<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"><channel rdf:about="http://onlinelibrary.wiley.com/rss/journal/10.1111/(ISSN)1654-109X" xmlns="http://purl.org/rss/1.0/"><title>Applied Vegetation Science</title><description> Wiley Online Library : Applied Vegetation Science</description><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2F%28ISSN%291654-109X</link><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc</dc:publisher><dc:language xmlns:dc="http://purl.org/dc/elements/1.1/">en</dc:language><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/">© International Association for Vegetation Science</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1402-2001</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1654-109X</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">April 2013</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">16</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">2</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">169</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">351</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/avsc.2013.16.issue-2/asset/cover.gif?v=1&amp;s=90a2670efd28e1041292ff903e94eeb0c8e556ed"/><items><rdf:Seq><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12048"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12047"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12046"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12039"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12034"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12042"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12044"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12038"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12040"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12037"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12036"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12033"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12032"/><rdf:li 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rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12023"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12018"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12017"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12021"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12019"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12016"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12009"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12013"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12004"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12011"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12007"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12006"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12003"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12005"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12014"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12022"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01221.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01227.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01222.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01228.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01220.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01215.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01226.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01224.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01218.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01216.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12001"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01217.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01225.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12000"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01223.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12002"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01219.x"/></rdf:Seq></items></channel><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12048" xmlns="http://purl.org/rss/1.0/"><title>Savanna woody vegetation classification – now in 3-D</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12048</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Savanna woody vegetation classification – now in 3-D</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jolene T. Fisher, Barend F.N. Erasmus, Ed T.F. Witkowski, Jan Aardt, Konrad J. Wessels, Gregory P. Asner</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-21T06:44:28.132747-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12048</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12048</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12048</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12048-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>The co-existence of woody plants and grasses characterize savannas, with the horizontal and vertical spatial arrangement of trees creating a heterogeneous biotic environment. To understand the influence of biogeophysical drivers on the spatial patterns of 3-D structure of woody vegetation, these patterns need to be explained over large areas to capture the context. Is there a spatially explicit, ecologically meaningful way to capture the patterns and context of 3-D woody vegetation structure?</p></div></div>
<div class="section" id="avsc12048-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Classification development and testing sites: landscapes in Bushbuckridge Municipality, Sabi Sand Wildtuin and Kruger National Park, Mpumalanga province, north-east South Africa.</p></div></div>
<div class="section" id="avsc12048-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>The aforementioned structural classification approach requires appropriate 3-D and spatially explicit remote sensing data. A LiDAR-based canopy height model (CHM) and volumetric pixel (voxel) data from the Carnegie Airborne Observatory Alpha system were used to create the structural classification. First, we segmented the CHM images using multi-threshold and multi-resolution image segmentation techniques, and classified the image segments into four height classes, namely shrub (1–3 m), low tree (3–6 m), high tree (6–10 m) or tall tree (&gt;10 m). A hierarchical <em>a priori</em> approach was used to develop classification criteria. The following metrics were calculated for 0.25-ha grid cells based on the cover and spatial arrangement of the four height classes: canopy cover, sub-canopy cover, canopy layers, Simpson's diversity index and cohesion. Top of canopy vegetation was classified using each metric at the 0.25-ha scale, with canopy cover being the primary classification metric. Subsequently, individual layers identified within the canopy were classified using the voxel data. We use a code system for describing classes to ensure standardization between different regions; a more traditional naming system may be used in addition for interpretation.</p></div></div>
<div class="section" id="avsc12048-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>This system provides a more comprehensive classification of the horizontal and vertical structural diversity of savannas compared to the traditional vegetation classification systems. The description of multi-layers within the canopy should allow for a sensitive change detection method. The classification can be used in many current focus areas, including habitat suitability mapping for biodiversity conservation, strategic adaptive management and monitoring land-cover change.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12048/asset/image_m/avsc12048-toc-0001-m.png?v=1&amp;s=9bdc3080e9511d8ad53a88b8247b394dace87c28" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12048/asset/image_n/avsc12048-toc-0001.gif?v=1&amp;s=7522b562bb29651162d0c91d063eb4cd637a46c1"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We developed a three-dimensional woody vegetation structural classification for savannas to capture the context of biogeophysical drivers. LiDAR (Light Detection and Ranging) data were used to calculate Canopy Cover, Sub-canopy Cover, Canopy Layers, Simpson's Diversity Index and Cohesion for 0.25 ha grid cells based on vertical and horizontal spatial arrangement of vegetation. The classification provides a sensitive change detection method.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
The co-existence of woody plants and grasses characterize savannas, with the horizontal and vertical spatial arrangement of trees creating a heterogeneous biotic environment. To understand the influence of biogeophysical drivers on the spatial patterns of 3-D structure of woody vegetation, these patterns need to be explained over large areas to capture the context. Is there a spatially explicit, ecologically meaningful way to capture the patterns and context of 3-D woody vegetation structure?


Location
Classification development and testing sites: landscapes in Bushbuckridge Municipality, Sabi Sand Wildtuin and Kruger National Park, Mpumalanga province, north-east South Africa.


Methods
The aforementioned structural classification approach requires appropriate 3-D and spatially explicit remote sensing data. A LiDAR-based canopy height model (CHM) and volumetric pixel (voxel) data from the Carnegie Airborne Observatory Alpha system were used to create the structural classification. First, we segmented the CHM images using multi-threshold and multi-resolution image segmentation techniques, and classified the image segments into four height classes, namely shrub (1–3 m), low tree (3–6 m), high tree (6–10 m) or tall tree (&gt;10 m). A hierarchical a priori approach was used to develop classification criteria. The following metrics were calculated for 0.25-ha grid cells based on the cover and spatial arrangement of the four height classes: canopy cover, sub-canopy cover, canopy layers, Simpson's diversity index and cohesion. Top of canopy vegetation was classified using each metric at the 0.25-ha scale, with canopy cover being the primary classification metric. Subsequently, individual layers identified within the canopy were classified using the voxel data. We use a code system for describing classes to ensure standardization between different regions; a more traditional naming system may be used in addition for interpretation.


Conclusion
This system provides a more comprehensive classification of the horizontal and vertical structural diversity of savannas compared to the traditional vegetation classification systems. The description of multi-layers within the canopy should allow for a sensitive change detection method. The classification can be used in many current focus areas, including habitat suitability mapping for biodiversity conservation, strategic adaptive management and monitoring land-cover change.

We developed a three-dimensional woody vegetation structural classification for savannas to capture the context of biogeophysical drivers. LiDAR (Light Detection and Ranging) data were used to calculate Canopy Cover, Sub-canopy Cover, Canopy Layers, Simpson's Diversity Index and Cohesion for 0.25 ha grid cells based on vertical and horizontal spatial arrangement of vegetation. The classification provides a sensitive change detection method.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12047" xmlns="http://purl.org/rss/1.0/"><title>Identifying the trait syndromes of conservation indicator species: how distinct are British ancient woodland indicator plants from other woodland species?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12047</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Identifying the trait syndromes of conservation indicator species: how distinct are British ancient woodland indicator plants from other woodland species?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adam Kimberley, George A. Blackburn, James D. Whyatt, Keith Kirby, Simon M. Smart</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-17T01:00:21.676224-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12047</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12047</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12047</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12047-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Ancient woodland indicator species (AWIs) are plant species which are thought to be restricted to areas of long-continuity woodland habitat. In many cases, however, these species have been identified on the basis of personal, to some extent, subjective experience. Do the species proposed as AWIs according to these lists have traits in common, and how distinct is their trait profile from that of other woodland plant species?</p></div></div>
<div class="section" id="avsc12047-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>United Kingdom.</p></div></div>
<div class="section" id="avsc12047-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We applied classification tree analysis to a plant trait database to assess the extent to which proposed AWI species can be clearly separated from other woodland plants based upon their traits. We contrasted AWI species with an objectively defined list of plants that are not considered to be AWIs but that have been commonly recorded in woodlands. We also investigate the effects of phylogeny and region specificity on species' proposed AWI status.</p></div></div>
<div class="section" id="avsc12047-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The results provide support for the distinctiveness of plant species thought to be associated with ancient woodland; they were found to be almost exclusively short, perennial species, usually with a high seed weight. Results also indicate that rarer AWIs have a more distinguishable trait profile than more common species. No link was found between phylogeny and AWI status.</p></div></div>
<div class="section" id="avsc12047-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>AWI species do have a distinguishable trait profile, despite their often partially subjective selection. The results of the classification tree analysis suggest that traits reflecting poor dispersal ability may be partly responsible for confining these species to ancient woodlands. This confirms other studies that emphasize their low ability to colonize secondary woodland sites and hence vulnerability to habitat conversion.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12047/asset/image_m/avsc12047-toc-0001-m.png?v=1&amp;s=c4e1e6fb89374ee2cf958167173577b47655b472" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12047/asset/image_n/avsc12047-toc-0001.gif?v=1&amp;s=659efab117b9c4ff0c91d0191833b84460c2c4d2"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Classification tree analysis was used to determine how effectively ancient woodland indicator plants can be distinguished based upon life history traits. Characteristics such as plant height and lifespan were effective in separating these species from other woodland plants. More common ancient woodland indicators were less successfully discriminated in this way however, and may potentially be less reliable as indicator species.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Ancient woodland indicator species (AWIs) are plant species which are thought to be restricted to areas of long-continuity woodland habitat. In many cases, however, these species have been identified on the basis of personal, to some extent, subjective experience. Do the species proposed as AWIs according to these lists have traits in common, and how distinct is their trait profile from that of other woodland plant species?


Location
United Kingdom.


Methods
We applied classification tree analysis to a plant trait database to assess the extent to which proposed AWI species can be clearly separated from other woodland plants based upon their traits. We contrasted AWI species with an objectively defined list of plants that are not considered to be AWIs but that have been commonly recorded in woodlands. We also investigate the effects of phylogeny and region specificity on species' proposed AWI status.


Results
The results provide support for the distinctiveness of plant species thought to be associated with ancient woodland; they were found to be almost exclusively short, perennial species, usually with a high seed weight. Results also indicate that rarer AWIs have a more distinguishable trait profile than more common species. No link was found between phylogeny and AWI status.


Conclusions
AWI species do have a distinguishable trait profile, despite their often partially subjective selection. The results of the classification tree analysis suggest that traits reflecting poor dispersal ability may be partly responsible for confining these species to ancient woodlands. This confirms other studies that emphasize their low ability to colonize secondary woodland sites and hence vulnerability to habitat conversion.

Classification tree analysis was used to determine how effectively ancient woodland indicator plants can be distinguished based upon life history traits. Characteristics such as plant height and lifespan were effective in separating these species from other woodland plants. More common ancient woodland indicators were less successfully discriminated in this way however, and may potentially be less reliable as indicator species.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12046" xmlns="http://purl.org/rss/1.0/"><title>Nitrogen and phosphorus fertilizer regime affect jarrah forest restoration after bauxite mining in Western Australia</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12046</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Nitrogen and phosphorus fertilizer regime affect jarrah forest restoration after bauxite mining in Western Australia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Matthew I. Daws, Rachel J. Standish, John M. Koch, Tim K. Morald</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-17T00:56:55.576437-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12046</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12046</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12046</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12046-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Removal of vegetation and disturbance of the soil profile during mining reduce nutrient pools available for plants during mine site restoration. Thus, fertilizer is needed to replace the loss of nutrients available to support vegetation establishment. Yet the application of fertilizer can promote the establishment of competitively dominant species to the exclusion of others, particularly in low-fertility ecosystems. Here, we test effects of fertilizer application rates on the establishment of jarrah forest.</p></div></div>
<div class="section" id="avsc12046-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Five restored mine pits in the jarrah forest that grows on low-fertility soils in southwest Western Australia.</p></div></div>
<div class="section" id="avsc12046-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Nitrogen (0 and 20 kg elemental N·ha<sup>−1</sup>) and phosphorus (0, 10, 20 and 40 kg elemental P·ha<sup>−1</sup>) were applied factorially to 20 m × 20 m field plots at five sites restored after bauxite mining with seeds and seedlings of jarrah forest species.</p></div></div>
<div class="section" id="avsc12046-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Two and a half years after the experiment was established, there were no effects of N application rates on species richness, percentage vegetation cover or community composition of the restored jarrah forest. In contrast, P application had a number of effects on the restored jarrah forest. Species richness was highest at intermediate P application rates (10–20 kg·ha<sup>−1</sup>) and lowest at the two extreme treatments (0 and 40 kg·ha<sup>−1</sup>). Higher rates of P application resulted in a higher seedling density (2.5 vs 5.0 m<sup>−2</sup> for 0 and 40 kg P·ha<sup>−1</sup>, respectively) and increased plant cover. Fertilizer P also significantly affected community composition, favouring ephemerals and weeds at high application rates and re-sprouting species at lower application rates. Community composition was more similar to the restoration target (unmined jarrah forest) at 0 kg·P·ha<sup>−1</sup> (similarity value of 36%) than at higher P application rates.</p></div></div>
<div class="section" id="avsc12046-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The data suggest that, in terms of maximizing species richness and percentage cover, a P application rate of between 10 kg·P·ha<sup>−1</sup>and 20 kg·P·ha<sup>−1</sup>is optimal for jarrah forest restoration after bauxite mining. Additionally, the data suggest no benefit of N application at a rate of 20 kg·N·ha<sup>−1</sup>.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12046/asset/image_m/avsc12046-toc-0001-m.png?v=1&amp;s=bf3d5666bd975950c8cf1d997faa8d71bf0494dd" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12046/asset/image_n/avsc12046-toc-0001.gif?v=1&amp;s=4c18588b91ded9d316e46f8fb69d2cdb871f4fed"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>To address loss of soil nutrients in the mining process, fertiliser is generally added in mine-site restoration. We investigated fertiliser effects on restoration outcomes for jarrah-forest restored after bauxite mining. Fertiliser-P significantly affected plant cover, species richness and community composition suggesting a trade-off between using fertiliser to stimulate rapid plant establishment to minimise erosion and achieving high species richness.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Removal of vegetation and disturbance of the soil profile during mining reduce nutrient pools available for plants during mine site restoration. Thus, fertilizer is needed to replace the loss of nutrients available to support vegetation establishment. Yet the application of fertilizer can promote the establishment of competitively dominant species to the exclusion of others, particularly in low-fertility ecosystems. Here, we test effects of fertilizer application rates on the establishment of jarrah forest.


Location
Five restored mine pits in the jarrah forest that grows on low-fertility soils in southwest Western Australia.


Methods
Nitrogen (0 and 20 kg elemental N·ha−1) and phosphorus (0, 10, 20 and 40 kg elemental P·ha−1) were applied factorially to 20 m × 20 m field plots at five sites restored after bauxite mining with seeds and seedlings of jarrah forest species.


Results
Two and a half years after the experiment was established, there were no effects of N application rates on species richness, percentage vegetation cover or community composition of the restored jarrah forest. In contrast, P application had a number of effects on the restored jarrah forest. Species richness was highest at intermediate P application rates (10–20 kg·ha−1) and lowest at the two extreme treatments (0 and 40 kg·ha−1). Higher rates of P application resulted in a higher seedling density (2.5 vs 5.0 m−2 for 0 and 40 kg P·ha−1, respectively) and increased plant cover. Fertilizer P also significantly affected community composition, favouring ephemerals and weeds at high application rates and re-sprouting species at lower application rates. Community composition was more similar to the restoration target (unmined jarrah forest) at 0 kg·P·ha−1 (similarity value of 36%) than at higher P application rates.


Conclusions
The data suggest that, in terms of maximizing species richness and percentage cover, a P application rate of between 10 kg·P·ha−1and 20 kg·P·ha−1is optimal for jarrah forest restoration after bauxite mining. Additionally, the data suggest no benefit of N application at a rate of 20 kg·N·ha−1.

To address loss of soil nutrients in the mining process, fertiliser is generally added in mine-site restoration. We investigated fertiliser effects on restoration outcomes for jarrah-forest restored after bauxite mining. Fertiliser-P significantly affected plant cover, species richness and community composition suggesting a trade-off between using fertiliser to stimulate rapid plant establishment to minimise erosion and achieving high species richness.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12039" xmlns="http://purl.org/rss/1.0/"><title>The effect of weed management systems and location on arable weed species communities in glyphosate-resistant cropping systems</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12039</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The effect of weed management systems and location on arable weed species communities in glyphosate-resistant cropping systems</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David J. Gibson, Karla L. Gage, Joseph L. Matthews, Bryan G. Young, Micheal D.K. Owen, Robert G. Wilson, Stephen C. Weller, David R. Shaw, David L. Jordan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T05:39:49.635428-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12039</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12039</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12039</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12039-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>How do different weed management systems based on glyphosate-resistant (GR) crops affect weed community structure and composition?</p></div></div>
<div class="section" id="avsc12039-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>A total of 156 agricultural fields across six US states.</p></div></div>
<div class="section" id="avsc12039-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Fields were selected and categorized into three weed management systems based on a 3-yr history: (1) a single continuous GR crop; (2) a rotation of two GR crops; and (3) a GR crop rotated with a non-GR crop. Weed species population density was surveyed in 20 0.5-m<sup>2</sup> plots per field four times each season from 2006 to 2010. Weed population density, species richness and diversity were analysed using repeated measures mixed models to test the effect of year, geographic location (based on plant hardiness zone) and weed management system (as described above). Weed community composition was analysed using NMDS ordination. The importance of geographic location, planted crop and weed management system were analysed using analysis of similarity and permutational ANOVA based on the Bray–Curtis similarity among sites calculated from the maximum weed species population density per site per year.</p></div></div>
<div class="section" id="avsc12039-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>A total of 329 weed species were identified across the six states and all time periods. Weed communities were most strongly correlated with geographic location and secondarily to the crop planted. Weed management system affected similarity among weed communities through an interaction with site location but not every year. The weed management systems of crop rotation and GR trait rotation generally reduced weed population density and species diversity, but the effect of crop rotation varied by geographic location.</p></div></div>
<div class="section" id="avsc12039-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The overall effects of weed management systems in fields including the GR trait on arable weed communities reinforce the need for locally adapted weed management programmes to steward the GR crop trait to manage for high weed diversity while reducing crop–weed competition and maximizing yield.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12039/asset/image_m/avsc12039-toc-0001-m.png?v=1&amp;s=d8d3a6682362a56068354215a6ebea1d42151ded" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12039/asset/image_n/avsc12039-toc-0001.gif?v=1&amp;s=34b4deffd6a7bb100057bf91d33a5eea5eba66cf"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Weed management systems that included the use of glyphosate-resistant crops had only a limited effect on arable weed species communities in 156 fields across six US states over five years. Rather, these communities were most affected by location and the crop planted. Locally-adapted management is required to maintain weed biodiversity while maximizing crop yield.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
How do different weed management systems based on glyphosate-resistant (GR) crops affect weed community structure and composition?


Location
A total of 156 agricultural fields across six US states.


Methods
Fields were selected and categorized into three weed management systems based on a 3-yr history: (1) a single continuous GR crop; (2) a rotation of two GR crops; and (3) a GR crop rotated with a non-GR crop. Weed species population density was surveyed in 20 0.5-m2 plots per field four times each season from 2006 to 2010. Weed population density, species richness and diversity were analysed using repeated measures mixed models to test the effect of year, geographic location (based on plant hardiness zone) and weed management system (as described above). Weed community composition was analysed using NMDS ordination. The importance of geographic location, planted crop and weed management system were analysed using analysis of similarity and permutational ANOVA based on the Bray–Curtis similarity among sites calculated from the maximum weed species population density per site per year.


Results
A total of 329 weed species were identified across the six states and all time periods. Weed communities were most strongly correlated with geographic location and secondarily to the crop planted. Weed management system affected similarity among weed communities through an interaction with site location but not every year. The weed management systems of crop rotation and GR trait rotation generally reduced weed population density and species diversity, but the effect of crop rotation varied by geographic location.


Conclusions
The overall effects of weed management systems in fields including the GR trait on arable weed communities reinforce the need for locally adapted weed management programmes to steward the GR crop trait to manage for high weed diversity while reducing crop–weed competition and maximizing yield.

Weed management systems that included the use of glyphosate-resistant crops had only a limited effect on arable weed species communities in 156 fields across six US states over five years. Rather, these communities were most affected by location and the crop planted. Locally-adapted management is required to maintain weed biodiversity while maximizing crop yield.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12034" xmlns="http://purl.org/rss/1.0/"><title>Fire impact on the woody plant components of dry deciduous forest in Central Menabe, Madagascar</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12034</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fire impact on the woody plant components of dry deciduous forest in Central Menabe, Madagascar</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tabea Ehrensperger, Zora Lea Urech, Maik Rehnus, Jean-Pierre Sorg</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T05:39:43.243781-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12034</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12034</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12034</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12034-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>We investigated the effects of human-induced fires on woody plant components of dry deciduous forest in Madagascar. Specifically, we addressed the following questions: (1) which forest layers are most affected by fire; (2) how is forest structure, species richness, diversity and composition affected by fire disturbance; and (3) does the forest recover after fire disturbance?</p></div></div>
<div class="section" id="avsc12034-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Kirindy Forest in Central Menabe, western Madagascar.</p></div></div>
<div class="section" id="avsc12034-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We conducted our investigations in seven areas of the Kirindy Forest, which was burned between 1984 and 2009. Vegetation data were collected in nested plots for the different forest layers in the burned and unburned forest. Using GLM, we assessed fire impact on forest structure, species richness and diversity of the different forest layers. The recovery of burned forest was investigated using correlation analysis. In addition, we used descriptive methods to analyse fire impact on species composition.</p></div></div>
<div class="section" id="avsc12034-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Fire mainly influenced the middle forest layers, trees &gt;1.50-m high and diameters &lt;15 cm, and significantly reduced tree density, basal area, species richness and diversity. Fire had no significant impact on the measured parameters of the shrub and top layers. Despite the severe impact of fire on the middle forest layers, most of the measured parameters of these layers were able to recover from fire disturbance within a short time. Twelve years after fire disturbance, tree density, basal area, species richness and diversity in burned forest areas no longer differed from unburned forest areas. However, species composition differed substantially between burned and unburned forests.</p></div></div>
<div class="section" id="avsc12034-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>We conclude that fire severely impacts the middle forest layers and alters forest structure, i.e. species richness and tree diversity, of the dry deciduous forest of Central Menabe.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12034/asset/image_m/avsc12034-toc-0001-m.png?v=1&amp;s=17365578fc04bf2eaadcd2dda53f2646f6984ff0" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12034/asset/image_n/avsc12034-toc-0001.gif?v=1&amp;s=39c887da9fc65a9dc151b266dbe1d48e1bba60d8"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We investigated the effects of human-induce fires on woody plant components a dry decidous forest. We conclude from our results that fire severely impacts the middle forest layers with trees higher than 1.50 m and diameters less than 15 cm and alters forest structure, including species richness and diversity of trees of the dry deciduous forest of Central Menabe.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
We investigated the effects of human-induced fires on woody plant components of dry deciduous forest in Madagascar. Specifically, we addressed the following questions: (1) which forest layers are most affected by fire; (2) how is forest structure, species richness, diversity and composition affected by fire disturbance; and (3) does the forest recover after fire disturbance?


Location
Kirindy Forest in Central Menabe, western Madagascar.


Methods
We conducted our investigations in seven areas of the Kirindy Forest, which was burned between 1984 and 2009. Vegetation data were collected in nested plots for the different forest layers in the burned and unburned forest. Using GLM, we assessed fire impact on forest structure, species richness and diversity of the different forest layers. The recovery of burned forest was investigated using correlation analysis. In addition, we used descriptive methods to analyse fire impact on species composition.


Results
Fire mainly influenced the middle forest layers, trees &gt;1.50-m high and diameters &lt;15 cm, and significantly reduced tree density, basal area, species richness and diversity. Fire had no significant impact on the measured parameters of the shrub and top layers. Despite the severe impact of fire on the middle forest layers, most of the measured parameters of these layers were able to recover from fire disturbance within a short time. Twelve years after fire disturbance, tree density, basal area, species richness and diversity in burned forest areas no longer differed from unburned forest areas. However, species composition differed substantially between burned and unburned forests.


Conclusions
We conclude that fire severely impacts the middle forest layers and alters forest structure, i.e. species richness and tree diversity, of the dry deciduous forest of Central Menabe.

We investigated the effects of human-induce fires on woody plant components a dry decidous forest. We conclude from our results that fire severely impacts the middle forest layers with trees higher than 1.50 m and diameters less than 15 cm and alters forest structure, including species richness and diversity of trees of the dry deciduous forest of Central Menabe.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12042" xmlns="http://purl.org/rss/1.0/"><title>A functional trait approach to fen restoration analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12042</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A functional trait approach to fen restoration analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Petter Hedberg, Peter Saetre, Sebastian Sundberg, Håkan Rydin, Wiktor Kotowski</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-30T04:33:07.783537-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12042</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12042</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12042</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12042-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>Ecological restoration has traditionally been evaluated with analyses focused on species identities and abundances. These analyses provide no ecological explanation to why certain species change in abundance. One solution may be a functional trait analysis. We asked whether shifts in functional traits could explain vegetation changes in fens restored through tree cutting and rewetting, and how the functional traits in the restored sites compare to those of the reference site?</p></div></div>
<div class="section" id="avsc12042-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Three former rich fens in east-central Sweden.</p></div></div>
<div class="section" id="avsc12042-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Tree cutting and rewetting were applied in a factorial design, and species and abundance data were recorded for 8 yrs. Abundance data and trait data of canopy height, specific leaf area (SLA) and diaspore mass were used to calculate functional richness (FRic), functional divergence (FDiv), functional dispersion (FDis) and community-weighted mean (CWM) of functional traits. Data were analysed in a linear mixed effect model for vascular plants and bryophytes jointly, and for vascular plants separately. Results of restoration treatments were compared to data from a reference site.</p></div></div>
<div class="section" id="avsc12042-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Among vascular plants, tree cutting caused a decrease in SLA, as shade-sensitive species increased. In accordance with the change in SLA, FDis increased. In the joint analysis, tree cutting led to increased FDis, FDiv and FRic, indicating reduced filtering caused by the removal of the shading canopy, which allowed shade-sensitive species to establish. The comparison to the reference site shows that even after 8 yrs, the restoration treatments have higher trait diversity than the reference site, indicating that the restoration sites have a too relaxed trait filter compared to conditions in an undisturbed fen. Our interpretation is that this is primarily caused by insufficient rewetting (and increased nutrient availability) that allow species of both natural and degraded fen conditions to co-exist, and which failed to suppress the regrowth of trees.</p></div></div>
<div class="section" id="avsc12042-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Analysis of functional diversity improves our understanding of the ecological mechanisms affecting restoration results, and allows comparison among regions and communities with different species composition.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12042/asset/image_m/avsc12042-toc-0001-m.png?v=1&amp;s=ada2a3375c8cc8c0b996119e883b0939b4dc48c7" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12042/asset/image_n/avsc12042-toc-0001.gif?v=1&amp;s=f5b6381e23d88dbe1107463e3efb92cbc34bc38c"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study is one of the first to use a functional trait analysis to analyse the outcome of ecological restoration. The study shows that a functional trait analysis can reveal trait changes caused by the restoration actions, as well as shed light on differences in functional trait composition between the restoration site and the reference site.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
Ecological restoration has traditionally been evaluated with analyses focused on species identities and abundances. These analyses provide no ecological explanation to why certain species change in abundance. One solution may be a functional trait analysis. We asked whether shifts in functional traits could explain vegetation changes in fens restored through tree cutting and rewetting, and how the functional traits in the restored sites compare to those of the reference site?


Location
Three former rich fens in east-central Sweden.


Methods
Tree cutting and rewetting were applied in a factorial design, and species and abundance data were recorded for 8 yrs. Abundance data and trait data of canopy height, specific leaf area (SLA) and diaspore mass were used to calculate functional richness (FRic), functional divergence (FDiv), functional dispersion (FDis) and community-weighted mean (CWM) of functional traits. Data were analysed in a linear mixed effect model for vascular plants and bryophytes jointly, and for vascular plants separately. Results of restoration treatments were compared to data from a reference site.


Results
Among vascular plants, tree cutting caused a decrease in SLA, as shade-sensitive species increased. In accordance with the change in SLA, FDis increased. In the joint analysis, tree cutting led to increased FDis, FDiv and FRic, indicating reduced filtering caused by the removal of the shading canopy, which allowed shade-sensitive species to establish. The comparison to the reference site shows that even after 8 yrs, the restoration treatments have higher trait diversity than the reference site, indicating that the restoration sites have a too relaxed trait filter compared to conditions in an undisturbed fen. Our interpretation is that this is primarily caused by insufficient rewetting (and increased nutrient availability) that allow species of both natural and degraded fen conditions to co-exist, and which failed to suppress the regrowth of trees.


Conclusions
Analysis of functional diversity improves our understanding of the ecological mechanisms affecting restoration results, and allows comparison among regions and communities with different species composition.

This study is one of the first to use a functional trait analysis to analyse the outcome of ecological restoration. The study shows that a functional trait analysis can reveal trait changes caused by the restoration actions, as well as shed light on differences in functional trait composition between the restoration site and the reference site.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12044" xmlns="http://purl.org/rss/1.0/"><title>Drought-induced woody plant mortality in an encroached semi-arid savanna depends on topoedaphic factors and land management</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12044</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Drought-induced woody plant mortality in an encroached semi-arid savanna depends on topoedaphic factors and land management</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dirac Twidwell, Carissa L. Wonkka, Charles A. Taylor, Chris B. Zou, Jeremiah J. Twidwell, William E. Rogers</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-30T04:32:06.538943-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12044</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12044</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12044</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12044-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How do recent patterns of drought-induced woody plant mortality in Texas semi-arid savanna compare to the extended drought of the 1950s? Does the relative composition of the woody plant community shift ubiquitously across the landscape following woody plant mortality and dieback or are shifts dependent on differences among species, soils, land use and plant demography?</p></div></div>
<div class="section" id="avsc12044-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Texas Agrilife Research Station, Sonora, Texas, USA (30.1° N 100.3° W).</p></div></div>
<div class="section" id="avsc12044-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Following an exceptional drought from 1951 to 1957, a study was conducted to quantify rates of mortality for various woody plant species. In 2011, we repeated this study within three long-term grazing treatments that were established in 1948. Ten transects were established in each treatment to quantify the frequency and cover of live and dead woody individuals for all woody species. Rates of woody plant dieback were determined for each species and tested for differences among height classes, soil categories, total woody densities and pastoral treatments.</p></div></div>
<div class="section" id="avsc12044-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Flash droughts (defined as rapidly intensifying droughts characterized by moisture deficits and high temperatures) from 2000 to 2011 were the second most severe since 1919 (low PDSI = −4) and were only surpassed by the prolonged drought from 1951 to 1957 (low PDSI = −5.17). Drought-induced shifts from one woody plant community to another did not occur uniformly across the landscape. Instead, high mortality rates of mature <em>Juniperus ashei</em> trees in deep soils (67.3%, 33 of 49 trees), combined with the recruitment of <em>Quercus</em> species where grazing had been excluded for the last 60 yr, were the only patch types to shift from a <em>Juniperus–Quercus</em> woodland to an alternate state.</p></div></div>
<div class="section" id="avsc12044-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Flash droughts since 2000 resulted in significant mortality and dieback, but dieback in cover was 28% higher following the more severe drought of the 1950s. Legacies from long-term land management practices interacted with localized differences in topoedaphic factors to drive patch-level shifts in woody vegetation following drought.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12044/asset/image_m/avsc12044-toc-0001-m.png?v=1&amp;s=88fc3d720e6fdee7a8acdec380262afc984a9f42" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12044/asset/image_n/avsc12044-toc-0001.gif?v=1&amp;s=718887e3cc553662ca84de1808ab562d57a0a946"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We repeated a historical field experiment to compare rates of woody mortality resulting from recent droughts to the exceptional drought of 1951–1957. Mortality was greater following the more severe drought of the 1950s than recent flash droughts from 2000 to 2011. Long-term land management legacies interacted with localized differences in topoedaphic factors to drive patch-level shifts in woody vegetation following drought.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How do recent patterns of drought-induced woody plant mortality in Texas semi-arid savanna compare to the extended drought of the 1950s? Does the relative composition of the woody plant community shift ubiquitously across the landscape following woody plant mortality and dieback or are shifts dependent on differences among species, soils, land use and plant demography?


Location
Texas Agrilife Research Station, Sonora, Texas, USA (30.1° N 100.3° W).


Methods
Following an exceptional drought from 1951 to 1957, a study was conducted to quantify rates of mortality for various woody plant species. In 2011, we repeated this study within three long-term grazing treatments that were established in 1948. Ten transects were established in each treatment to quantify the frequency and cover of live and dead woody individuals for all woody species. Rates of woody plant dieback were determined for each species and tested for differences among height classes, soil categories, total woody densities and pastoral treatments.


Results
Flash droughts (defined as rapidly intensifying droughts characterized by moisture deficits and high temperatures) from 2000 to 2011 were the second most severe since 1919 (low PDSI = −4) and were only surpassed by the prolonged drought from 1951 to 1957 (low PDSI = −5.17). Drought-induced shifts from one woody plant community to another did not occur uniformly across the landscape. Instead, high mortality rates of mature Juniperus ashei trees in deep soils (67.3%, 33 of 49 trees), combined with the recruitment of Quercus species where grazing had been excluded for the last 60 yr, were the only patch types to shift from a Juniperus–Quercus woodland to an alternate state.


Conclusions
Flash droughts since 2000 resulted in significant mortality and dieback, but dieback in cover was 28% higher following the more severe drought of the 1950s. Legacies from long-term land management practices interacted with localized differences in topoedaphic factors to drive patch-level shifts in woody vegetation following drought.

We repeated a historical field experiment to compare rates of woody mortality resulting from recent droughts to the exceptional drought of 1951–1957. Mortality was greater following the more severe drought of the 1950s than recent flash droughts from 2000 to 2011. Long-term land management legacies interacted with localized differences in topoedaphic factors to drive patch-level shifts in woody vegetation following drought.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12038" xmlns="http://purl.org/rss/1.0/"><title>Fifty years of tree line change in the Khibiny Mountains, Russia: advantages of combined remote sensing and dendroecological approaches</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12038</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fifty years of tree line change in the Khibiny Mountains, Russia: advantages of combined remote sensing and dendroecological approaches</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ingrid E. Mathisen, Anna Mikheeva, Olga V. Tutubalina, Sigrun Aune, Annika Hofgaard</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-25T05:01:34.3227-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12038</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12038</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12038</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12038-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>Tree line ecotone regions are expected to respond swiftly to climate changes. In this paper, remote sensing- and ground-based tree population data are used to examine past and on-going changes of the tree line ecotone in a sub-arctic region characterized by precipitation increase. Questions addressed are: (1) at what rate has the tree line ecotone changed since the mid-20th century; (2) can specific temporal dynamics be identified; and (3) do combined remote sensing and tree population analyses add essential knowledge for the interpretation of tree line changes?</p></div></div>
<div class="section" id="avsc12038-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Khibiny Mountains, Kola Peninsula, northwest Russia.</p></div></div>
<div class="section" id="avsc12038-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Aerial photos from 1958, high-resolution satellite imagery from 2006/2008 and age structure data for dominant tree line species (birch and pine) were used to analyse rate of change and temporal and species-specific tree line recruitment patterns. This was accomplished using digital elevation models, resolution-merging procedures, visual interpretation and dendroecological methods.</p></div></div>
<div class="section" id="avsc12038-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Mean tree line advance for birch and pine was recorded as 29 and 27 altitudinal metres (0.6 and 0.5 m·yr<sup>−1</sup>), respectively. The advance was accompanied by an apparent infilling of pre-established tree populations and by recruitment beyond the tree line. Evident increased recruitment occurred in the late 1980s for birch and in the 1970s and 1990s for pine. Establishment showed no strong correlations with climate variables, but the importance of non-growing season variables was indicated.</p></div></div>
<div class="section" id="avsc12038-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The recorded tree line advance is modest compared to global model predictions for advance at high latitudes, but in accordance with results from a number of high-latitude areas. Concomitantly, the apparent increased recruitment is indicative of a more rapidly advancing tree line zone. Studies combining remote sensing and ground-based data minimize the risk of under- or overestimating potential tree line advance. Low detectability of small seedlings and saplings by remote sensing can cause underestimation of the current potential, while ground-based data used alone can overestimate potential advance. A balance between the two approaches is beneficial and enhances quality in production of change scenarios related to high latitudinal tree line areas at local to large regional scales.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12038/asset/image_m/avsc12038-toc-0001-m.png?v=1&amp;s=bfbacf647d0a122fa98257b0b810e0f2f7dbc40a" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12038/asset/image_n/avsc12038-toc-0001.gif?v=1&amp;s=9231c196692cc3eff05f7f773d313b96498de1b4"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Subarctic treelines are commonly predicted to show pronounced advance in response to climate change. This study, combining remote sensing techniques and ground based age structure data, shows modest rates. Studies combining these methods minimize the risk of under- or overestimating potential advance.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
Tree line ecotone regions are expected to respond swiftly to climate changes. In this paper, remote sensing- and ground-based tree population data are used to examine past and on-going changes of the tree line ecotone in a sub-arctic region characterized by precipitation increase. Questions addressed are: (1) at what rate has the tree line ecotone changed since the mid-20th century; (2) can specific temporal dynamics be identified; and (3) do combined remote sensing and tree population analyses add essential knowledge for the interpretation of tree line changes?


Location
Khibiny Mountains, Kola Peninsula, northwest Russia.


Methods
Aerial photos from 1958, high-resolution satellite imagery from 2006/2008 and age structure data for dominant tree line species (birch and pine) were used to analyse rate of change and temporal and species-specific tree line recruitment patterns. This was accomplished using digital elevation models, resolution-merging procedures, visual interpretation and dendroecological methods.


Results
Mean tree line advance for birch and pine was recorded as 29 and 27 altitudinal metres (0.6 and 0.5 m·yr−1), respectively. The advance was accompanied by an apparent infilling of pre-established tree populations and by recruitment beyond the tree line. Evident increased recruitment occurred in the late 1980s for birch and in the 1970s and 1990s for pine. Establishment showed no strong correlations with climate variables, but the importance of non-growing season variables was indicated.


Conclusions
The recorded tree line advance is modest compared to global model predictions for advance at high latitudes, but in accordance with results from a number of high-latitude areas. Concomitantly, the apparent increased recruitment is indicative of a more rapidly advancing tree line zone. Studies combining remote sensing and ground-based data minimize the risk of under- or overestimating potential tree line advance. Low detectability of small seedlings and saplings by remote sensing can cause underestimation of the current potential, while ground-based data used alone can overestimate potential advance. A balance between the two approaches is beneficial and enhances quality in production of change scenarios related to high latitudinal tree line areas at local to large regional scales.

Subarctic treelines are commonly predicted to show pronounced advance in response to climate change. This study, combining remote sensing techniques and ground based age structure data, shows modest rates. Studies combining these methods minimize the risk of under- or overestimating potential advance.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12040" xmlns="http://purl.org/rss/1.0/"><title>Differences in spatial autocorrelation (SAc), plant species richness and diversity, and plant community composition in grazed and ungrazed grasslands along a moisture gradient, North Dakota, USA</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12040</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Differences in spatial autocorrelation (SAc), plant species richness and diversity, and plant community composition in grazed and ungrazed grasslands along a moisture gradient, North Dakota, USA</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lindsey M. Meyers, Edward S. DeKeyser, Jack E. Norland</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-17T03:24:37.253004-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12040</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12040</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12040</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12040-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How are plant species richness and diversity related to spatial autocorrelation under grazed and ungrazed conditions in grassland communities? Is spatial autocorrelation dissimilar within different plant communities?</p></div></div>
<div class="section" id="avsc12040-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>The grasslands of southeast North Dakota, USA.</p></div></div>
<div class="section" id="avsc12040-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>The study was conducted during the summer of 2009 in six grasslands under different management (grazed vs ungrazed with fire) along a moisture gradient. Spatial autocorrelation at each site was measured along 50-m transects among three different landscape positions representing different moisture levels. Dissimogram multivariate analysis was used to measure the nugget, dissimilarity and patch diameter. Additionally, richness and Shannon diversity indices and nonmetric multidimensional scaling analysis were compared to the dissimogram results.</p></div></div>
<div class="section" id="avsc12040-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Mean patch diameter was significantly higher in grazed mid-slope sites than in ungrazed sites. Spatial autocorrelation was not different between the landscape positions (higher, dry areas were not different from lower, mesic areas). However, plant species richness, diversity and community composition were found to be different between landscape positions and management, with key differences in the presence of certain invasive species.</p></div></div>
<div class="section" id="avsc12040-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Disturbance and moisture level were reflected differently in the spatial autocorrelation analysis compared to the richness, diversity and ordination analyses. This indicates that disturbance and management impacted spatial autocorrelation separate from plant community composition and species diversity. This also highlights changes in the plant community caused by different management actions and the spread of invasive species.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12040/asset/image_m/avsc12040-toc-0001-m.png?v=1&amp;s=d2890119855b5d7797a6a22e406f88203a2dd115" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12040/asset/image_n/avsc12040-toc-0001.gif?v=1&amp;s=93170b6e8c6345ed9138aa237ac7993da52fd73c"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Our study was conducted within plant communities in grasslands that were either grazed or ungrazed. We compared spatial autocorrelation to richness, Shannon diversity, and Nonmetric Multidimensional Scaling. We found that disturbance and moisture level were reflected differently in the different analyses. Spatial autocorrelation is another tool that can be used by managers to analyze plant communities and make decisions.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How are plant species richness and diversity related to spatial autocorrelation under grazed and ungrazed conditions in grassland communities? Is spatial autocorrelation dissimilar within different plant communities?


Location
The grasslands of southeast North Dakota, USA.


Methods
The study was conducted during the summer of 2009 in six grasslands under different management (grazed vs ungrazed with fire) along a moisture gradient. Spatial autocorrelation at each site was measured along 50-m transects among three different landscape positions representing different moisture levels. Dissimogram multivariate analysis was used to measure the nugget, dissimilarity and patch diameter. Additionally, richness and Shannon diversity indices and nonmetric multidimensional scaling analysis were compared to the dissimogram results.


Results
Mean patch diameter was significantly higher in grazed mid-slope sites than in ungrazed sites. Spatial autocorrelation was not different between the landscape positions (higher, dry areas were not different from lower, mesic areas). However, plant species richness, diversity and community composition were found to be different between landscape positions and management, with key differences in the presence of certain invasive species.


Conclusions
Disturbance and moisture level were reflected differently in the spatial autocorrelation analysis compared to the richness, diversity and ordination analyses. This indicates that disturbance and management impacted spatial autocorrelation separate from plant community composition and species diversity. This also highlights changes in the plant community caused by different management actions and the spread of invasive species.

Our study was conducted within plant communities in grasslands that were either grazed or ungrazed. We compared spatial autocorrelation to richness, Shannon diversity, and Nonmetric Multidimensional Scaling. We found that disturbance and moisture level were reflected differently in the different analyses. Spatial autocorrelation is another tool that can be used by managers to analyze plant communities and make decisions.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12037" xmlns="http://purl.org/rss/1.0/"><title>Choosing a DIVA: a comparison of emerging digital imagery vegetation analysis techniques</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12037</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Choosing a DIVA: a comparison of emerging digital imagery vegetation analysis techniques</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christopher F. Jorgensen, Ryan J. Stutzman, Lars C. Anderson, Suzanne E. Decker, Larkin A. Powell, Walter H. Schacht, Joseph J. Fontaine</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-13T00:16:59.672143-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12037</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12037</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12037</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12037-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>What is the precision of five methods of measuring vegetation structure using ground-based digital imagery and processing techniques?</p></div></div>
<div class="section" id="avsc12037-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Lincoln, Nebraska, USA</p></div></div>
<div class="section" id="avsc12037-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Vertical herbaceous cover was recorded using digital imagery techniques at two distinct locations in a mixed-grass prairie. The precision of five ground-based digital imagery vegetation analysis (DIVA) methods for measuring vegetation structure was tested using a split-split plot analysis of covariance. Variability within each DIVA technique was estimated using coefficient of variation of mean percentage cover.</p></div></div>
<div class="section" id="avsc12037-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Vertical herbaceous cover estimates differed among DIVA techniques. Additionally, environmental conditions affected the vertical vegetation obstruction estimates for certain digital imagery methods, while other techniques were more adept at handling various conditions. Overall, percentage vegetation cover values differed among techniques, but the precision of four of the five techniques was consistently high.</p></div></div>
<div class="section" id="avsc12037-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>DIVA procedures are sufficient for measuring various heights and densities of standing herbaceous cover. Moreover, digital imagery techniques can reduce measurement error associated with multiple observers' standing herbaceous cover estimates, allowing greater opportunity to detect patterns associated with vegetation structure.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12037/asset/image_m/avsc12037-toc-0001-m.png?v=1&amp;s=ac1c263b6cc1700723ec2863d5681cafabd5ed8b" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12037/asset/image_n/avsc12037-toc-0001.gif?v=1&amp;s=875a98a28cf12a45e23bbf8aa65a4c57382cff95"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We examined the precision of five methods of measuring vertical herbaceous cover using ground-based digital imagery vegetation analysis (DIVA) techniques. Although environmental conditions affected the vertical vegetation obstruction estimates, certain DIVA techniques were capable of accounting for various conditions. Overall, four of the five DIVA techniques proved sufficient for measuring standing herbaceous cover and reduced error associated with multiple observers.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
What is the precision of five methods of measuring vegetation structure using ground-based digital imagery and processing techniques?


Location
Lincoln, Nebraska, USA


Methods
Vertical herbaceous cover was recorded using digital imagery techniques at two distinct locations in a mixed-grass prairie. The precision of five ground-based digital imagery vegetation analysis (DIVA) methods for measuring vegetation structure was tested using a split-split plot analysis of covariance. Variability within each DIVA technique was estimated using coefficient of variation of mean percentage cover.


Results
Vertical herbaceous cover estimates differed among DIVA techniques. Additionally, environmental conditions affected the vertical vegetation obstruction estimates for certain digital imagery methods, while other techniques were more adept at handling various conditions. Overall, percentage vegetation cover values differed among techniques, but the precision of four of the five techniques was consistently high.


Conclusions
DIVA procedures are sufficient for measuring various heights and densities of standing herbaceous cover. Moreover, digital imagery techniques can reduce measurement error associated with multiple observers' standing herbaceous cover estimates, allowing greater opportunity to detect patterns associated with vegetation structure.

We examined the precision of five methods of measuring vertical herbaceous cover using ground-based digital imagery vegetation analysis (DIVA) techniques. Although environmental conditions affected the vertical vegetation obstruction estimates, certain DIVA techniques were capable of accounting for various conditions. Overall, four of the five DIVA techniques proved sufficient for measuring standing herbaceous cover and reduced error associated with multiple observers.





</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12036" xmlns="http://purl.org/rss/1.0/"><title>Edges, exotics and deer: the seed bank of a suburban secondary successional temperate deciduous forest</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12036</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Edges, exotics and deer: the seed bank of a suburban secondary successional temperate deciduous forest</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vanessa B. Beauchamp, Nureen Ghuznavi, Stephanie M. Koontz, Roland P. Roberts</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-02T07:20:29.480342-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12036</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12036</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12036</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12036-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>(1) What is the utility of the soil seed bank in passive restoration of a suburban secondary successional temperate deciduous forest? (2) What is the composition and structure of the seed bank? (3) How abundant are woody and exotic species and how are they distributed in the seed bank? (4) Are edge effects evident in seed bank composition? (5) What is the influence of a suite of abiotic and biotic variables, including deer browse, on seed bank richness and abundance?</p></div></div>
<div class="section" id="avsc12036-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>A 413-ha suburban forest near Baltimore, Maryland, USA.</p></div></div>
<div class="section" id="avsc12036-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We sampled the seed bank and vegetation of 100 permanent plots in a <em>Liriodendron</em>–<em>Fagus</em>–<em>Acer</em>–<em>Quercus</em> dominated secondary successional forest. Information on soil chemistry, canopy cover, leaf litter cover and depth, deer browse severity and distance to the nearest urban edge and path was also collected for each plot. Seedling emergence was monitored in a greenhouse over 2 yr.</p></div></div>
<div class="section" id="avsc12036-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>A total of 76 species emerged from the seed bank, including 16 woody species and 22 exotic species. Compositional similarity between the seed bank and vegetation was low. Woody species were under-represented and exotic species were over-represented, with exotic species found in the seed bank of 94 of 100 plots. Species composition and exotic species richness and abundance were similar between edge or path and interior plots. Leaf litter cover, vegetation cover, browse severity and variables related to soil fertility were included in top models explaining patterns in seed bank richness and abundance.</p></div></div>
<div class="section" id="avsc12036-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Reliance on the soil seed bank as a passive restoration strategy will be insufficient for restoring a mature secondary successional suburban forest community. However, a suite of shade-tolerant exotic shrubs and vines that are of concern to management do not appear to use the seed bank, indicating that targeted removal of these species may be successful. Increased deer browse was associated with decreased seed bank abundance and richness, suggesting that deer may directly reduce inputs to the seed bank. If deer are impacting seed bank composition, active restoration will need to include understorey herbs in addition to overstorey species.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12036/asset/image_m/avsc12036-toc-0001-m.png?v=1&amp;s=e25b944871e49ec103f2b890d458864058036c7f" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12036/asset/image_n/avsc12036-toc-0001.gif?v=1&amp;s=a5feacf07515f0d2db78cfdbffe71d4af1c9cc0c"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The seed bank contained 76 species with overrepresentation of exotic species and underrepresentation of woody species. Exotic species occurred throughout the entire property and high deer browse was correlated with decreased seed bank abundance and richness. Reliance on the soil seed bank as a passive restoration strategy will be insufficient for restoring a mature secondary successional suburban forest community.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
(1) What is the utility of the soil seed bank in passive restoration of a suburban secondary successional temperate deciduous forest? (2) What is the composition and structure of the seed bank? (3) How abundant are woody and exotic species and how are they distributed in the seed bank? (4) Are edge effects evident in seed bank composition? (5) What is the influence of a suite of abiotic and biotic variables, including deer browse, on seed bank richness and abundance?


Location
A 413-ha suburban forest near Baltimore, Maryland, USA.


Methods
We sampled the seed bank and vegetation of 100 permanent plots in a Liriodendron–Fagus–Acer–Quercus dominated secondary successional forest. Information on soil chemistry, canopy cover, leaf litter cover and depth, deer browse severity and distance to the nearest urban edge and path was also collected for each plot. Seedling emergence was monitored in a greenhouse over 2 yr.


Results
A total of 76 species emerged from the seed bank, including 16 woody species and 22 exotic species. Compositional similarity between the seed bank and vegetation was low. Woody species were under-represented and exotic species were over-represented, with exotic species found in the seed bank of 94 of 100 plots. Species composition and exotic species richness and abundance were similar between edge or path and interior plots. Leaf litter cover, vegetation cover, browse severity and variables related to soil fertility were included in top models explaining patterns in seed bank richness and abundance.


Conclusions
Reliance on the soil seed bank as a passive restoration strategy will be insufficient for restoring a mature secondary successional suburban forest community. However, a suite of shade-tolerant exotic shrubs and vines that are of concern to management do not appear to use the seed bank, indicating that targeted removal of these species may be successful. Increased deer browse was associated with decreased seed bank abundance and richness, suggesting that deer may directly reduce inputs to the seed bank. If deer are impacting seed bank composition, active restoration will need to include understorey herbs in addition to overstorey species.

The seed bank contained 76 species with overrepresentation of exotic species and underrepresentation of woody species. Exotic species occurred throughout the entire property and high deer browse was correlated with decreased seed bank abundance and richness. Reliance on the soil seed bank as a passive restoration strategy will be insufficient for restoring a mature secondary successional suburban forest community.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12033" xmlns="http://purl.org/rss/1.0/"><title>Soil biota of different size classes change the impact of soil compaction on a plant community</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12033</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Soil biota of different size classes change the impact of soil compaction on a plant community</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mara E. Beck, Susanne Wurst</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-30T01:52:42.200888-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12033</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12033</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12033</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12033-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Does a reduction in size class of soil biota aggravate the impacts of soil compaction on plant communities?</p></div></div>
<div class="section" id="avsc12033-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Controlled mesocosm study with a European ruderal plant community exposed to soil compaction and soil biota communities of different size classes.</p></div></div>
<div class="section" id="avsc12033-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We evaluated the individual and combined effects of soil compaction and soil biota communities of different size classes (&lt;2000, &lt;212, &lt;20 μm, natural control) on the structure and productivity of a ruderal plant community, and the establishment of a neophyte (<em>Lupinus polyphyllus</em>) in a full-factorial mesocosm study.</p></div></div>
<div class="section" id="avsc12033-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Soil compaction reduced the productivity of the plant community, but the negative effect decreased in magnitude as the size class of the soil biota community was reduced. Consistently, shoot growth of the dominant grasses was most reduced by soil compaction when bigger soil biota were present; the shoot growth of forbs showed an opposite pattern. In contrast, legumes seem to profit from soil compaction independent of the size class of the soil biota community, and were detrimentally affected only in the natural control soil. Establishment of the neophyte <em>L. polyphyllus</em> was best under natural soil conditions and was not affected by soil compaction.</p></div></div>
<div class="section" id="avsc12033-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>A reduction in soil biota size due to intensified management may change the impacts of soil compaction on plant communities. The results indicate that soil compaction has the most detrimental effect on primary productivity in soil communities where a range of size classes of soil biota is present and the functional complexity of the soil biota community is therefore high.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12033/asset/image_m/avsc12033-toc-0001-m.png?v=1&amp;s=ebce07db2ed177f7f2e5c24b454990a6fcbcca06" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12033/asset/image_n/avsc12033-toc-0001.gif?v=1&amp;s=5c97613d45cd281ccb931290a21e3a8721b8d6cd"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Soil compaction and a reduction in soil biota size classes are common consequences of intensified land use. Our results show that a reduction of soil biota sizes may change the impact of soil compaction on plant communities. The most detrimental effects of soil compaction were detected in soils with a range of soil biota size classes and thus higher complexity.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Does a reduction in size class of soil biota aggravate the impacts of soil compaction on plant communities?


Location
Controlled mesocosm study with a European ruderal plant community exposed to soil compaction and soil biota communities of different size classes.


Methods
We evaluated the individual and combined effects of soil compaction and soil biota communities of different size classes (&lt;2000, &lt;212, &lt;20 μm, natural control) on the structure and productivity of a ruderal plant community, and the establishment of a neophyte (Lupinus polyphyllus) in a full-factorial mesocosm study.


Results
Soil compaction reduced the productivity of the plant community, but the negative effect decreased in magnitude as the size class of the soil biota community was reduced. Consistently, shoot growth of the dominant grasses was most reduced by soil compaction when bigger soil biota were present; the shoot growth of forbs showed an opposite pattern. In contrast, legumes seem to profit from soil compaction independent of the size class of the soil biota community, and were detrimentally affected only in the natural control soil. Establishment of the neophyte L. polyphyllus was best under natural soil conditions and was not affected by soil compaction.


Conclusions
A reduction in soil biota size due to intensified management may change the impacts of soil compaction on plant communities. The results indicate that soil compaction has the most detrimental effect on primary productivity in soil communities where a range of size classes of soil biota is present and the functional complexity of the soil biota community is therefore high.

Soil compaction and a reduction in soil biota size classes are common consequences of intensified land use. Our results show that a reduction of soil biota sizes may change the impact of soil compaction on plant communities. The most detrimental effects of soil compaction were detected in soils with a range of soil biota size classes and thus higher complexity.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12032" xmlns="http://purl.org/rss/1.0/"><title>Effects of changes in management on resistance and resilience in three grassland communities</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12032</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effects of changes in management on resistance and resilience in three grassland communities</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leoš Klimeš, Michal Hájek, Ondřej Mudrák, Martin Dančák, Zdenka Preislerová, Petra Hájková, Ivana Jongepierová, Jitka Klimešová</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-12T09:22:23.80261-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12032</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12032</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12032</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12032-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Diversification of grassland management is recommended as a tool for conservation of different taxonomic groups living in those habitats. How resistant and resilient are species-rich grasslands in terms of plant species richness and vegetation composition to short-term, small-scale perturbations caused by changes in management practice?</p></div></div>
<div class="section" id="avsc12032-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Bílé Karpaty Mountains, SE Czech Republic.</p></div></div>
<div class="section" id="avsc12032-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>The experiment included the effect of six management regimes (mowing in June; mowing in September; mowing in June and September; mowing in June and high stubble left; no management; mowing in June and mulching). It was conducted in species-rich wooded grasslands in the White Carpathians Mts., Czech Republic, represented by three types of plant community: a <em>Bromus erectus</em> community (with high species richness and low productivity), a <em>Molinia arundinacea</em> community (with high species richness and high productivity), and a <em>Calamagrostis epigejos</em> community (with low species richness and high productivity). After 3 yr, resistance was assessed, and traditional management (mowing once each year in June) was resumed; resilience was evaluated after three more years.</p></div></div>
<div class="section" id="avsc12032-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>While the species-rich, unproductive <em>Bromus</em> community was relatively resistant to less intensive management in terms of species richness, and therefore its resilience could not be assessed, it changed substantially in terms of vegetation composition (maximum dissimilarity between control and abandoned plots was 63%). The more productive <em>Molinia</em> and <em>Calamagrostis</em> communities lost up to 37% of species due to abandonment, but not as a consequence of other changes management regimes. After the traditional management was resumed, resilience was higher in the <em>Calamagrostis</em> community than in the <em>Molinia</em> community. Vegetation composition was not affected by treatments.</p></div></div>
<div class="section" id="avsc12032-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The results show that short-term abandonment causes loss of plant diversity in productive grasslands but not in less productive, species-rich grasslands in the short term. Other relaxed management regimes (e.g. high stubble and delayed mowing) were comparable with the control and can be used for a short time to increase diversity of management without an effect on plant species richness. However, further research is needed to assess the effects of these management practices when they are applied repeatedly or over the long term.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12032/asset/image_m/avsc12032-toc-0001-m.png?v=1&amp;s=0d911fac832f1233652120c5986cecbe257085a1" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12032/asset/image_n/avsc12032-toc-0001.gif?v=1&amp;s=39fdbfad5ffbf263f85d8672cc93b583b763c056"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Diversification of grassland management is recommended as a tool for conservation of different taxonomical groups. We studied plant response in species-rich grasslands to short-term changes in management practice. Abandonment but not other relaxed management regimes (high stubble, delayed mowing) caused loss of plant diversity in productive grasslands but not in less productive grasslands. Grassland productivity should be considered when applying relaxed management in grassland.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Diversification of grassland management is recommended as a tool for conservation of different taxonomic groups living in those habitats. How resistant and resilient are species-rich grasslands in terms of plant species richness and vegetation composition to short-term, small-scale perturbations caused by changes in management practice?


Location
Bílé Karpaty Mountains, SE Czech Republic.


Methods
The experiment included the effect of six management regimes (mowing in June; mowing in September; mowing in June and September; mowing in June and high stubble left; no management; mowing in June and mulching). It was conducted in species-rich wooded grasslands in the White Carpathians Mts., Czech Republic, represented by three types of plant community: a Bromus erectus community (with high species richness and low productivity), a Molinia arundinacea community (with high species richness and high productivity), and a Calamagrostis epigejos community (with low species richness and high productivity). After 3 yr, resistance was assessed, and traditional management (mowing once each year in June) was resumed; resilience was evaluated after three more years.


Results
While the species-rich, unproductive Bromus community was relatively resistant to less intensive management in terms of species richness, and therefore its resilience could not be assessed, it changed substantially in terms of vegetation composition (maximum dissimilarity between control and abandoned plots was 63%). The more productive Molinia and Calamagrostis communities lost up to 37% of species due to abandonment, but not as a consequence of other changes management regimes. After the traditional management was resumed, resilience was higher in the Calamagrostis community than in the Molinia community. Vegetation composition was not affected by treatments.


Conclusions
The results show that short-term abandonment causes loss of plant diversity in productive grasslands but not in less productive, species-rich grasslands in the short term. Other relaxed management regimes (e.g. high stubble and delayed mowing) were comparable with the control and can be used for a short time to increase diversity of management without an effect on plant species richness. However, further research is needed to assess the effects of these management practices when they are applied repeatedly or over the long term.

Diversification of grassland management is recommended as a tool for conservation of different taxonomical groups. We studied plant response in species-rich grasslands to short-term changes in management practice. Abandonment but not other relaxed management regimes (high stubble, delayed mowing) caused loss of plant diversity in productive grasslands but not in less productive grasslands. Grassland productivity should be considered when applying relaxed management in grassland.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12030" xmlns="http://purl.org/rss/1.0/"><title>Post-fire regeneration in Mediterranean reforested sites as affected by mechanical site preparation: lessons for restoration</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12030</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Post-fire regeneration in Mediterranean reforested sites as affected by mechanical site preparation: lessons for restoration</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nurit Hibsher, Yossi Moshe, Eitan Bney-Moshe, Ezra Ben-Moshe, Ela Zangi, Aviram Zuck, Yagil Osem</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-06T03:28:57.146572-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12030</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12030</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12030</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12030-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>The importance of silvicultural site preparation techniques in determining vegetation succession is increasingly recognized. We studied the effects of mechanical site preparation (MSP) on post-fire vegetation regeneration within reforested sites in Mediterranean Israel.</p></div></div>
<div class="section" id="avsc12030-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Upper Galilee region, Israel.</p></div></div>
<div class="section" id="avsc12030-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Vegetation cover and composition, ruderal species colonization and pine regeneration were monitored in four reforested sites for 3 yr following wildland fires that burned mature <em>Pinus brutia</em> and <em>P. halepensis</em> plantations. In each reforested site, a 50 m × 50 m monitoring area was assigned and measurements were conducted within five subplots (2 m × 50 m) encompassing three MSP patch types: ploughed patches (P), unploughed patches (UP) and planting mounds (M) that combined ploughing, pit digging and wood-chip mulching.</p></div></div>
<div class="section" id="avsc12030-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Recovery of vegetation cover (excluding pines) was rapid. The MSP patch type significantly affected vegetation cover in the first spring following the fire: cover was lowest on M, intermediate on P and highest on UP. However, these differences became minor by the third spring following the fire. Total woody species richness was not affected by MSP patch type, although there were minor effects on relative abundance of woody species. Two ruderal species were found, but their abundance became untraceable by the third year. Patterns of MSP effects on pine regeneration were similar for <em>P. halepensis</em> and <em>P. brutia</em>. Density of emerging seedlings of both pine species during the first year following the fire was significantly affected by MSP patch type: lower in P and M than in UP by more than 50% and 90%, respectively. However, emergence and/or survival during the following 2 yr was higher in P and M than in UP, with overall outcome of pine regeneration still about 50% lower in P and M than in UP.</p></div></div>
<div class="section" id="avsc12030-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The MSP treatments had only a minor, short-term effect on post-fire regeneration and colonization of vegetation, except for pine recruitment, which was more severely affected.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12030/asset/image_m/avsc12030-toc-0001-m.png?v=1&amp;s=28c146793e3e96a6e032d5edc9fc000daedfb882" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12030/asset/image_n/avsc12030-toc-0001.gif?v=1&amp;s=6e4300d85f77ed14f9e8862adbc4ec877961c06c"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Biria forest, November 2006, following the wildland fire which occurred in the previous summer (August). Salvage logging was already applied in part of the burned area.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
The importance of silvicultural site preparation techniques in determining vegetation succession is increasingly recognized. We studied the effects of mechanical site preparation (MSP) on post-fire vegetation regeneration within reforested sites in Mediterranean Israel.


Location
Upper Galilee region, Israel.


Methods
Vegetation cover and composition, ruderal species colonization and pine regeneration were monitored in four reforested sites for 3 yr following wildland fires that burned mature Pinus brutia and P. halepensis plantations. In each reforested site, a 50 m × 50 m monitoring area was assigned and measurements were conducted within five subplots (2 m × 50 m) encompassing three MSP patch types: ploughed patches (P), unploughed patches (UP) and planting mounds (M) that combined ploughing, pit digging and wood-chip mulching.


Results
Recovery of vegetation cover (excluding pines) was rapid. The MSP patch type significantly affected vegetation cover in the first spring following the fire: cover was lowest on M, intermediate on P and highest on UP. However, these differences became minor by the third spring following the fire. Total woody species richness was not affected by MSP patch type, although there were minor effects on relative abundance of woody species. Two ruderal species were found, but their abundance became untraceable by the third year. Patterns of MSP effects on pine regeneration were similar for P. halepensis and P. brutia. Density of emerging seedlings of both pine species during the first year following the fire was significantly affected by MSP patch type: lower in P and M than in UP by more than 50% and 90%, respectively. However, emergence and/or survival during the following 2 yr was higher in P and M than in UP, with overall outcome of pine regeneration still about 50% lower in P and M than in UP.


Conclusions
The MSP treatments had only a minor, short-term effect on post-fire regeneration and colonization of vegetation, except for pine recruitment, which was more severely affected.

Biria forest, November 2006, following the wildland fire which occurred in the previous summer (August). Salvage logging was already applied in part of the burned area.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12025" xmlns="http://purl.org/rss/1.0/"><title>Classification of Taiwan forest vegetation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12025</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Classification of Taiwan forest vegetation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ching-Feng Li, Milan Chytrý, David Zelený, Ming-Yih Chen, Tze-Ying Chen, Chyi-Rong Chiou, Yue-Joe Hsia, Ho-Yih Liu, Sheng-Zehn Yang, Ching-Long Yeh, Jenn-Che Wang, Chiou-Feng Yu, Yen-Jen Lai, Wei-Chun Chao, Chang-Fu Hsieh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-06T00:17:04.191182-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12025</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12025</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12025</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12025-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Aim</h4><div class="para"><p>We identify the main forest vegetation types in Taiwan, provide their formal definitions and describe their species composition, habitat affinities and distribution.</p></div></div>
<div class="section" id="avsc12025-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Taiwan.</p></div></div>
<div class="section" id="avsc12025-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>A data set of 9822 vegetation plots with environmental characteristics recorded in the field or derived from digital maps in GIS was compiled from historical literature and an extensive field survey. Using expert knowledge, 6574 of these plots were used to build a classification into broad vegetation types. The units of the resulting classification were formally defined using a Cocktail determination key, which can be used for the automatic assignment of new vegetation plots to these vegetation types.</p></div></div>
<div class="section" id="avsc12025-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Twelve vegetation types of zonal forests and nine types of azonal forests were distinguished. Zonal types in the subtropical region, from high mountains to foothills, are <em>Juniperus</em> subalpine coniferous woodland, <em>Abies–Tsuga</em> upper-montane coniferous forest, <em>Chamaecyparis</em> montane mixed cloud forest, <em>Fagus</em> montane deciduous broad-leaved cloud forest, <em>Quercus</em> montane evergreen broad-leaved cloud forest, <em>Machilus–Castanopsis</em> sub-montane evergreen broad-leaved forest, <em>Phoebe</em>–<em>Machilus</em> sub-montane evergreen broad-leaved forest and <em>Ficus</em>–<em>Machilus</em> semi-evergreen foothill forest. Zonal types in the tropical region, from high mountains to foothills, are <em>Pasania</em>–<em>Elaeocarpus</em> montane evergreen broad-leaved cloud forest, <em>Drypetes</em>–<em>Helicia</em> sub-montane evergreen broad-leaved forest, <em>Dysoxylum–Machilus</em> foothill evergreen broad-leaved forest and <em>Aglaia</em>–<em>Ficus</em> foothill evergreen broad-leaved forest. Azonal types are <em>Illicium</em>–<em>Cyclobalanopsis</em> tropical winter monsoon forest, <em>Pyrenaria</em>–<em>Machilus</em> subtropical winter monsoon forest, <em>Diospyros</em>–<em>Champereia</em> tropical rock-outcrop forest, <em>Zelkova–Quercus</em> subtropical rock-outcrop forest, <em>Pinus</em> successional woodland, <em>Alnus</em> successional woodland, <em>Trema–Mallotus</em> successional woodland, <em>Scaevola–Hibiscus</em> seashore woodland and <em>Kandelia</em> mangrove.</p></div></div>
<div class="section" id="avsc12025-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The diversity of forest vegetation in Taiwan is strongly structured by the temperature and moisture gradient. Along the temperature gradient, five altitudinal zones can be recognized. Azonal forest types develop at sites affected by the winter monsoon, on steep slopes, rocky soils, in seashore saline habitats and in places disturbed by fire, landslides and human activities. Zonal vegetation contains a higher ratio of endemic and Pacific species and occurs in wetter habitats, whereas azonal vegetation contains co-existing species from different regions and usually occurs in drier habitats.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12025/asset/image_m/avsc12025-toc-0001-m.png?v=1&amp;s=618b2b2df4794cf9cac0b518e741ff11e551a2fa" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12025/asset/image_n/avsc12025-toc-0001.gif?v=1&amp;s=b68bb25b70ec6f8fbc8a5900ffc57db08f105b55"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This paper is the first description of subtropical Eastern Asia's forest vegetation in a broad scale using large vegetation database. It is also the first vegetation classification scheme applying the azonal concept in this region. The result of classification is formalized by Cocktail Determination Key (CoDeK). A R-based program and example plots for running CoDeK are provided in the appendices.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Aim
We identify the main forest vegetation types in Taiwan, provide their formal definitions and describe their species composition, habitat affinities and distribution.


Location
Taiwan.


Methods
A data set of 9822 vegetation plots with environmental characteristics recorded in the field or derived from digital maps in GIS was compiled from historical literature and an extensive field survey. Using expert knowledge, 6574 of these plots were used to build a classification into broad vegetation types. The units of the resulting classification were formally defined using a Cocktail determination key, which can be used for the automatic assignment of new vegetation plots to these vegetation types.


Results
Twelve vegetation types of zonal forests and nine types of azonal forests were distinguished. Zonal types in the subtropical region, from high mountains to foothills, are Juniperus subalpine coniferous woodland, Abies–Tsuga upper-montane coniferous forest, Chamaecyparis montane mixed cloud forest, Fagus montane deciduous broad-leaved cloud forest, Quercus montane evergreen broad-leaved cloud forest, Machilus–Castanopsis sub-montane evergreen broad-leaved forest, Phoebe–Machilus sub-montane evergreen broad-leaved forest and Ficus–Machilus semi-evergreen foothill forest. Zonal types in the tropical region, from high mountains to foothills, are Pasania–Elaeocarpus montane evergreen broad-leaved cloud forest, Drypetes–Helicia sub-montane evergreen broad-leaved forest, Dysoxylum–Machilus foothill evergreen broad-leaved forest and Aglaia–Ficus foothill evergreen broad-leaved forest. Azonal types are Illicium–Cyclobalanopsis tropical winter monsoon forest, Pyrenaria–Machilus subtropical winter monsoon forest, Diospyros–Champereia tropical rock-outcrop forest, Zelkova–Quercus subtropical rock-outcrop forest, Pinus successional woodland, Alnus successional woodland, Trema–Mallotus successional woodland, Scaevola–Hibiscus seashore woodland and Kandelia mangrove.


Conclusions
The diversity of forest vegetation in Taiwan is strongly structured by the temperature and moisture gradient. Along the temperature gradient, five altitudinal zones can be recognized. Azonal forest types develop at sites affected by the winter monsoon, on steep slopes, rocky soils, in seashore saline habitats and in places disturbed by fire, landslides and human activities. Zonal vegetation contains a higher ratio of endemic and Pacific species and occurs in wetter habitats, whereas azonal vegetation contains co-existing species from different regions and usually occurs in drier habitats.

This paper is the first description of subtropical Eastern Asia's forest vegetation in a broad scale using large vegetation database. It is also the first vegetation classification scheme applying the azonal concept in this region. The result of classification is formalized by Cocktail Determination Key (CoDeK). A R-based program and example plots for running CoDeK are provided in the appendices.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12031" xmlns="http://purl.org/rss/1.0/"><title>Phytosociology and ecology of the high-alpine to subnival scree vegetation of N and NW Iran (Alborz and Azerbaijan Mts.)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12031</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Phytosociology and ecology of the high-alpine to subnival scree vegetation of N and NW Iran (Alborz and Azerbaijan Mts.)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jalil Noroozi, Wolfgang Willner, Harald Pauli, Georg Grabherr</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-06T00:16:38.755553-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12031</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12031</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12031</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12031-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>The vegetation of high-alpine and subnival scree habitats in Iranian mountains has been poorly investigated so far despite the large variety of narrowly distributed vascular plant species and the expected vulnerability of these ecosystems to global warming. Which plant communities occupy these ecosystems and what is their syntaxonomic position? Which environmental factors determine the species composition of these habitats?</p></div></div>
<div class="section" id="avsc12031-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Alborz and Azerbaijan Mountains in N and NW Iran.</p></div></div>
<div class="section" id="avsc12031-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>A total of 141 phytosociological relevés were collected from 3200 to 4800 m a.s.l. This data set was classified using TWINSPAN, and the numerical classification was translated into a syntaxonomic system. Floristic differences between vegetation types were evaluated with detrended correspondence analysis (DCA). We determined the means and SD of measured environmental and vegetation parameters for all associations. Differences in the major environmental parameters among associations and alliances were analysed using ANOVA and <em>post-hoc</em> tests. Moreover, we determined the mean cover percentage of life forms in all associations.</p></div></div>
<div class="section" id="avsc12031-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>All high-alpine and subnival scree communities are arranged in one class (<em>Didymophyso aucheri-Dracocephaletea aucheri</em>), two orders (<em>Physoptychio gnaphalodis-Brometalia tomentosi</em>,<em> Didymophysetalia aucheri</em>), three alliances (<em>Elymo longearistati-Astragalion macrosemii</em>,<em> Erigerontion venusti</em>,<em> Didymophysion aucheri</em>) and ten associations, which are new to science, except for one association. The territory of the class extends from Alborz to NW Iran and probably to E Anatolia, Transcaucasia and the Zagros Mountains. Altitude, aspect and edaphic qualities are the major ecological factors influencing the species composition and vegetation mosaic.</p></div></div>
<div class="section" id="avsc12031-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Our study introduces a formal syntaxonomic classification of the scree vegetation at high altitudes in Iran, thus providing a scheme for ongoing ecological surveys and monitoring programmes to assess the impacts of climate warming and of human land use on these unique ecosystems.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12031/asset/image_m/avsc12031-toc-0001-m.png?v=1&amp;s=c363495b63b3078ff5b3c2d2c3bf75ae6999c3d8" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12031/asset/image_n/avsc12031-toc-0001.gif?v=1&amp;s=7f3248b73f4c57dc7e5f2277ebeff8fb99594c2f"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In this study we investigated the vegetation of high alpine and subnival scree habitats in high mountains of N and NW Iran. Altitude, aspect and soil conditions are the major ecological factors determining species composition of the studied vegetation types. We present a new classification scheme arranging the communities in one class, two orders, three alliances and ten associations.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
The vegetation of high-alpine and subnival scree habitats in Iranian mountains has been poorly investigated so far despite the large variety of narrowly distributed vascular plant species and the expected vulnerability of these ecosystems to global warming. Which plant communities occupy these ecosystems and what is their syntaxonomic position? Which environmental factors determine the species composition of these habitats?


Location
Alborz and Azerbaijan Mountains in N and NW Iran.


Methods
A total of 141 phytosociological relevés were collected from 3200 to 4800 m a.s.l. This data set was classified using TWINSPAN, and the numerical classification was translated into a syntaxonomic system. Floristic differences between vegetation types were evaluated with detrended correspondence analysis (DCA). We determined the means and SD of measured environmental and vegetation parameters for all associations. Differences in the major environmental parameters among associations and alliances were analysed using ANOVA and post-hoc tests. Moreover, we determined the mean cover percentage of life forms in all associations.


Results
All high-alpine and subnival scree communities are arranged in one class (Didymophyso aucheri-Dracocephaletea aucheri), two orders (Physoptychio gnaphalodis-Brometalia tomentosi, Didymophysetalia aucheri), three alliances (Elymo longearistati-Astragalion macrosemii, Erigerontion venusti, Didymophysion aucheri) and ten associations, which are new to science, except for one association. The territory of the class extends from Alborz to NW Iran and probably to E Anatolia, Transcaucasia and the Zagros Mountains. Altitude, aspect and edaphic qualities are the major ecological factors influencing the species composition and vegetation mosaic.


Conclusions
Our study introduces a formal syntaxonomic classification of the scree vegetation at high altitudes in Iran, thus providing a scheme for ongoing ecological surveys and monitoring programmes to assess the impacts of climate warming and of human land use on these unique ecosystems.

In this study we investigated the vegetation of high alpine and subnival scree habitats in high mountains of N and NW Iran. Altitude, aspect and soil conditions are the major ecological factors determining species composition of the studied vegetation types. We present a new classification scheme arranging the communities in one class, two orders, three alliances and ten associations.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12029" xmlns="http://purl.org/rss/1.0/"><title>Elevated nitrogen effects on Bromus tectorum dominance and native plant diversity in an arid montane ecosystem</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12029</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Elevated nitrogen effects on Bromus tectorum dominance and native plant diversity in an arid montane ecosystem</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Amy L. Concilio, Michael E. Loik</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-05T01:05:12.92951-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12029</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12029</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12029</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12029-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>Dominance of the widespread fire-altering invasive grass, <em>Bromus tectorum,</em> is markedly reduced at upper elevations in the Great Basin Desert. Here, we evaluated whether increased anthropogenic nitrogen (N) deposition would have an effect on species composition and ecosystem invasibility by <em>B. tectorum</em> at high elevations, and whether <em>B. tectorum</em> cover was associated with decreased native plant diversity.</p></div></div>
<div class="section" id="avsc12029-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Sagebrush steppe of the eastern Sierra Nevada, CA, US, at the western edge of the Great Basin Desert.</p></div></div>
<div class="section" id="avsc12029-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We set up 54 paired plots, half of which were exposed to elevated N deposition (50 kg·ha<sup>−1</sup>·yr<sup>−1</sup> at the time of snowmelt for 4 yr) and half acted as controls, in areas differing in disturbance history (grazed, burned and grazed–burned). We monitored species composition each summer from 2008 to 2011 and then compared species richness, Shannon's diversity (<em>H</em>'), Simpson's dominance (<em>D</em>'), Simpson's evenness (<em>E</em><sub>1/D</sub>), <em>B. tectorum</em> dominance and community similarity (with ANOSIM and SIMPER analyses) by N treatment and disturbance history.</p></div></div>
<div class="section" id="avsc12029-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Species composition differed by disturbance history in all years (ANOSIM,<em> P</em> &lt; 0.05), and the grazed–burned plots consistently had the highest levels of <em>B. tectorum</em> dominance (<em>P</em> ≤ 0.0003) and cover (<em>P</em> ≤ 0.0001). <em>Bromus tectorum</em> cover was inversely related to native forb species richness (<em>r</em> = −0.44, <em>P</em> &lt; 0.0001), <em>H</em>'(<em>r</em><sub><em>s</em></sub> = −0.73, <em>P</em> &lt; 0.0001), -ln(<em>D</em>') (<em>r</em><sub><em>s</em></sub> = −0.75, <em>P</em> &lt; 0.0001) and <em>E</em><sub>1/D</sub>'(<em>r</em><sub><em>s</em></sub> = −0.49, <em>P</em> &lt; 0.0001). We found no evidence that increased N deposition would affect native plant diversity after 4 yr in this arid montane ecosystem, but the possibility of longer-term effects cannot be eliminated.</p></div></div>
<div class="section" id="avsc12029-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Results suggest that high-elevation plant communities are already experiencing invasion impacts even though changes to the fire cycle have not yet occurred. In the most disturbed areas, <em>B. tectorum</em> cover is approaching the threshold for increased fire risk, which could result in more severe impacts at high elevations.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12029/asset/image_m/avsc12029-toc-0001-m.png?v=1&amp;s=ee2e7c5030f84c94a4aa3733882fe944bdcea5ca" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12029/asset/image_n/avsc12029-toc-0001.gif?v=1&amp;s=9f43902c45311774acb2013e3819a1f43bcf6578"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We evaluated how increased nitrogen deposition might affect dominance of the invasive annual grass, <em>Bromus tectorum,</em> at one of its high elevation range margins. Although we found no evidence that nitrogen would affect its spread, our results indicated that <em>B. tectorum</em> cover was negatively associated with native forb diversity, which is notable at such an early stage of invasion.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
Dominance of the widespread fire-altering invasive grass, Bromus tectorum, is markedly reduced at upper elevations in the Great Basin Desert. Here, we evaluated whether increased anthropogenic nitrogen (N) deposition would have an effect on species composition and ecosystem invasibility by B. tectorum at high elevations, and whether B. tectorum cover was associated with decreased native plant diversity.


Location
Sagebrush steppe of the eastern Sierra Nevada, CA, US, at the western edge of the Great Basin Desert.


Methods
We set up 54 paired plots, half of which were exposed to elevated N deposition (50 kg·ha−1·yr−1 at the time of snowmelt for 4 yr) and half acted as controls, in areas differing in disturbance history (grazed, burned and grazed–burned). We monitored species composition each summer from 2008 to 2011 and then compared species richness, Shannon's diversity (H'), Simpson's dominance (D'), Simpson's evenness (E1/D), B. tectorum dominance and community similarity (with ANOSIM and SIMPER analyses) by N treatment and disturbance history.


Results
Species composition differed by disturbance history in all years (ANOSIM, P &lt; 0.05), and the grazed–burned plots consistently had the highest levels of B. tectorum dominance (P ≤ 0.0003) and cover (P ≤ 0.0001). Bromus tectorum cover was inversely related to native forb species richness (r = −0.44, P &lt; 0.0001), H'(rs = −0.73, P &lt; 0.0001), -ln(D') (rs = −0.75, P &lt; 0.0001) and E1/D'(rs = −0.49, P &lt; 0.0001). We found no evidence that increased N deposition would affect native plant diversity after 4 yr in this arid montane ecosystem, but the possibility of longer-term effects cannot be eliminated.


Conclusions
Results suggest that high-elevation plant communities are already experiencing invasion impacts even though changes to the fire cycle have not yet occurred. In the most disturbed areas, B. tectorum cover is approaching the threshold for increased fire risk, which could result in more severe impacts at high elevations.

We evaluated how increased nitrogen deposition might affect dominance of the invasive annual grass, Bromus tectorum, at one of its high elevation range margins. Although we found no evidence that nitrogen would affect its spread, our results indicated that B. tectorum cover was negatively associated with native forb diversity, which is notable at such an early stage of invasion.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12028" xmlns="http://purl.org/rss/1.0/"><title>High-resolution remote sensing data improves models of species richness</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12028</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">High-resolution remote sensing data improves models of species richness</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Linda Camathias, Ariel Bergamini, Meinrad Küchler, Silvia Stofer, Andri Baltensweiler</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T01:30:41.135788-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12028</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12028</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12028</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12028-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Can predictors derived from air- and space-borne high-resolution remote sensing data improve models of species richness commonly built using coarser-scaled environmental variables?</p></div></div>
<div class="section" id="avsc12028-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Switzerland, covering 41 244 km<sup>2</sup> of Central Europe.</p></div></div>
<div class="section" id="avsc12028-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We applied linear regressions to model species richness of woody species, herbs, edaphic bryophytes and epiphytic lichens in Swiss forests. We included high-resolution predictors derived from digital height models and from satellite spectral images. Coarser-scaled predictors characterizing climatic and topographic conditions were also included, as were soil properties and geology. We applied hierarchical partitioning to regression models to investigate the independent contribution of each predictor set to species richness models.</p></div></div>
<div class="section" id="avsc12028-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Predictors derived from high-resolution remote sensing data substantially improved the species richness models (increase 14–55% of <em>R</em><sup>2</sup>). However, coarse-scaled climatic and topographic predictors still explained a high proportion of the variance in the species richness data in all models, independently of other predictors commonly used. The importance of the remotely sensed variables was strongly dependent on the biogeographic region considered. The species richness models of smaller organisms of the forest floor (herbs and edaphic bryophytes) benefited greatly from adding high-resolution topographic predictors, indicating the importance of microtopographic heterogeneity for these groups. Both epiphytic lichens and herbs responded strongly to indicators of structural properties of the forest stand.</p></div></div>
<div class="section" id="avsc12028-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>High-resolution remote sensing data is a proxy for micro-environmental structures and variation in these structures. Our results show that predictors derived from such data can improve species richness models considerably, especially in regions with low climatic and/or topographic variation. High-resolution remote sensing variables excellently complement coarser-scaled predictors, as they are available over large areas at low cost.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12028/asset/image_m/avsc12028-toc-0001-m.png?v=1&amp;s=b035f8f4d4eadb557e7304658ed1bc9412ad9939" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12028/asset/image_n/avsc12028-toc-0001.gif?v=1&amp;s=d335be0ada56c5568c7579843e7a1da496e101e8"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We studied if predictors derived from high resolution remote sensing data can improve models of species richness. We found that such predictors substantially improved species richness models. Improvement, however, depended on biogeographic regions and the species group considered. We concluded that high-resolution predictors excellently complement more commonly used coarser-scaled predictors as they are available over large areas at low cost.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Can predictors derived from air- and space-borne high-resolution remote sensing data improve models of species richness commonly built using coarser-scaled environmental variables?


Location
Switzerland, covering 41 244 km2 of Central Europe.


Methods
We applied linear regressions to model species richness of woody species, herbs, edaphic bryophytes and epiphytic lichens in Swiss forests. We included high-resolution predictors derived from digital height models and from satellite spectral images. Coarser-scaled predictors characterizing climatic and topographic conditions were also included, as were soil properties and geology. We applied hierarchical partitioning to regression models to investigate the independent contribution of each predictor set to species richness models.


Results
Predictors derived from high-resolution remote sensing data substantially improved the species richness models (increase 14–55% of R2). However, coarse-scaled climatic and topographic predictors still explained a high proportion of the variance in the species richness data in all models, independently of other predictors commonly used. The importance of the remotely sensed variables was strongly dependent on the biogeographic region considered. The species richness models of smaller organisms of the forest floor (herbs and edaphic bryophytes) benefited greatly from adding high-resolution topographic predictors, indicating the importance of microtopographic heterogeneity for these groups. Both epiphytic lichens and herbs responded strongly to indicators of structural properties of the forest stand.


Conclusions
High-resolution remote sensing data is a proxy for micro-environmental structures and variation in these structures. Our results show that predictors derived from such data can improve species richness models considerably, especially in regions with low climatic and/or topographic variation. High-resolution remote sensing variables excellently complement coarser-scaled predictors, as they are available over large areas at low cost.

We studied if predictors derived from high resolution remote sensing data can improve models of species richness. We found that such predictors substantially improved species richness models. Improvement, however, depended on biogeographic regions and the species group considered. We concluded that high-resolution predictors excellently complement more commonly used coarser-scaled predictors as they are available over large areas at low cost.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12026" xmlns="http://purl.org/rss/1.0/"><title>Soil seed banks of remnant and degraded Swartland Shale Renosterveld</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12026</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Soil seed banks of remnant and degraded Swartland Shale Renosterveld</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Steffen Heelemann, Cornelia B. Krug, Karen J. Esler, Christoph Reisch, Peter Poschlod</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-28T01:55:39.844018-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12026</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12026</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12026</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12026-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>What are the characteristics of soil seed banks in highly endangered renosterveld vegetation and adjacent degraded sites? What is the contribution of the soil seed bank to restoring renosterveld vegetation after degradation through agriculture or afforestation?</p></div></div>
<div class="section" id="avsc12026-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Tygerberg Nature Reserve – one of the largest remaining fragments of Swartland Shale Renosterveld, Cape Floristic Region, South Africa.</p></div></div>
<div class="section" id="avsc12026-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Assessment of vegetation, soil parameters and soil seed banks in three renosterveld sites, two adjacent abandoned fields, one pine plantation and one pine plantation clear-cut site. Smoke primer (i.e. fire surrogate) was applied to soil seed bank samples to evaluate fire as a possible management and restoration tool.</p></div></div>
<div class="section" id="avsc12026-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Abandoned agricultural fields adjacent to renosterveld remnants are characterized by alien grass cover, nutrient enrichment of the soil and depletion of the indigenous soil seed bank. In contrast, pine plantations show less alien species infestation, soil nutrient alteration and have a viable soil seed bank as well as re-development of indigenous renosterveld vegetation after clearance. Seedling recruitment was not significantly influenced by application of a smoke primer compared to the magnitude of fire response in fynbos.</p></div></div>
<div class="section" id="avsc12026-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Abandoned agricultural fields (previously renosterveld) at Tygerberg have a very low restoration potential. In contrast, pine plantation sites should be given priority in restoration, because soil chemistry is less significantly altered and a viable indigenous soil seed bank is still present, which can be successfully activated through clearance management.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12026/asset/image_m/avsc12026-toc-0001-m.png?v=1&amp;s=2704de4fe00c40906e97b1266883dfcbae591407" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12026/asset/image_n/avsc12026-toc-0001.gif?v=1&amp;s=f62b6ba679a159e19cb06409ee2f21518d6ad771"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The Tygerberg is one of the largest remaining fragments of threatended renosterveld vegetation in South Africa. Here, it was found that abandoned agricultural fields have a very low restoration potential. In contrast, pine plantation sites should be given priority in restoration with soil chemistry less significantly altered and a viable indigenous soil seed bank still present.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
What are the characteristics of soil seed banks in highly endangered renosterveld vegetation and adjacent degraded sites? What is the contribution of the soil seed bank to restoring renosterveld vegetation after degradation through agriculture or afforestation?


Location
Tygerberg Nature Reserve – one of the largest remaining fragments of Swartland Shale Renosterveld, Cape Floristic Region, South Africa.


Methods
Assessment of vegetation, soil parameters and soil seed banks in three renosterveld sites, two adjacent abandoned fields, one pine plantation and one pine plantation clear-cut site. Smoke primer (i.e. fire surrogate) was applied to soil seed bank samples to evaluate fire as a possible management and restoration tool.


Results
Abandoned agricultural fields adjacent to renosterveld remnants are characterized by alien grass cover, nutrient enrichment of the soil and depletion of the indigenous soil seed bank. In contrast, pine plantations show less alien species infestation, soil nutrient alteration and have a viable soil seed bank as well as re-development of indigenous renosterveld vegetation after clearance. Seedling recruitment was not significantly influenced by application of a smoke primer compared to the magnitude of fire response in fynbos.


Conclusion
Abandoned agricultural fields (previously renosterveld) at Tygerberg have a very low restoration potential. In contrast, pine plantation sites should be given priority in restoration, because soil chemistry is less significantly altered and a viable indigenous soil seed bank is still present, which can be successfully activated through clearance management.

The Tygerberg is one of the largest remaining fragments of threatended renosterveld vegetation in South Africa. Here, it was found that abandoned agricultural fields have a very low restoration potential. In contrast, pine plantation sites should be given priority in restoration with soil chemistry less significantly altered and a viable indigenous soil seed bank still present.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12027" xmlns="http://purl.org/rss/1.0/"><title>The role of domestic goats in the conservation of four endangered species of cactus: between dispersers and predators</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12027</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The role of domestic goats in the conservation of four endangered species of cactus: between dispersers and predators</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Baraza, S. Fernández-Osores</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-28T01:55:33.110121-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12027</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12027</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12027</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12027-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>The aim of this study was to establish the potential of domestic goats to act as cactus seed dispersers by assessing: (1) the proportion of cactus seeds that can pass undamaged through the domestic goat gut, (2) the temporal pattern of seed defecation, (3) whether ingestion by goats enhances or depresses cactus seed germination, and (4) whether the viable cactus seeds contained within goat faecal pellets can germinate directly from the faeces.</p></div></div>
<div class="section" id="avsc12027-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>River basin of Zapotitlán, Tehuacán-Cuicatlán Biosphere Reserve, Mexico.</p></div></div>
<div class="section" id="avsc12027-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Four groups of goats, each comprising three females of similar size and age, were fed the fruits of four endemic cactus species (<em>Echinocactus platyacanthus</em> f. <em>grandis, Ferocactus flavovirens, F. robustus</em> and <em>F. latispinus</em> var<em>. spiralis</em>). The percentage of undamaged seeds in the goat faeces was calculated at different times of collection following ingestion. Recovered seeds were tested for germination and viability, alongside seeds taken directly from the fruit. Intact and artificially cracked faecal pellets, collected from grazed natural areas, were kept in a greenhouse while seedling emergence was quantified. After 103 d, all cactus seeds that remained within the faecal pellets were recovered and their germination capacity was compared to that of the seeds taken directly from fruits.</p></div></div>
<div class="section" id="avsc12027-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>For the four species, between 28% and 61% of the seeds ingested were later recovered in the faecal pellets. No significant differences were found between species in the proportion of seeds retrieved during each collection time point. However, the time interval between ingestion and collection significantly influenced the number of seeds retrieved, peaking at between 16–32 hr. The digestion process significantly decreased the seed germination rate. Cactus germination from cracked faecal pellets was significantly higher than from intact pellets. Both contained viable seeds of all four cactus species, but particularly <em>E. platyacanthus</em> f. <em>grandis</em>.</p></div></div>
<div class="section" id="avsc12027-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Domestic goats are potential dispersers of the studied cactus species, although degradation of the faecal pellets is necessary to fully permit seedling emergence. These findings should be taken into account when designing management plans to conserve these endangered species.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12027/asset/image_m/avsc12027-toc-0001-m.png?v=1&amp;s=96c7640eb7fd871b26a319fa2e44af5c1ef4c543" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12027/asset/image_n/avsc12027-toc-0001.gif?v=1&amp;s=06f6c4f00bb31550d92c004ded85efecab80a5cd"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study analyzed the role of domestic goat as disperser of four endangered and endemic species of cacti. We analyzed the survival of seed after passage through the digestive tract of the goat and evaluated the capacity of viable seeds to germinate directly from fecal pellets. Our results show that domestic goat are potential dispersers of these species.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
The aim of this study was to establish the potential of domestic goats to act as cactus seed dispersers by assessing: (1) the proportion of cactus seeds that can pass undamaged through the domestic goat gut, (2) the temporal pattern of seed defecation, (3) whether ingestion by goats enhances or depresses cactus seed germination, and (4) whether the viable cactus seeds contained within goat faecal pellets can germinate directly from the faeces.


Location
River basin of Zapotitlán, Tehuacán-Cuicatlán Biosphere Reserve, Mexico.


Methods
Four groups of goats, each comprising three females of similar size and age, were fed the fruits of four endemic cactus species (Echinocactus platyacanthus f. grandis, Ferocactus flavovirens, F. robustus and F. latispinus var. spiralis). The percentage of undamaged seeds in the goat faeces was calculated at different times of collection following ingestion. Recovered seeds were tested for germination and viability, alongside seeds taken directly from the fruit. Intact and artificially cracked faecal pellets, collected from grazed natural areas, were kept in a greenhouse while seedling emergence was quantified. After 103 d, all cactus seeds that remained within the faecal pellets were recovered and their germination capacity was compared to that of the seeds taken directly from fruits.


Results
For the four species, between 28% and 61% of the seeds ingested were later recovered in the faecal pellets. No significant differences were found between species in the proportion of seeds retrieved during each collection time point. However, the time interval between ingestion and collection significantly influenced the number of seeds retrieved, peaking at between 16–32 hr. The digestion process significantly decreased the seed germination rate. Cactus germination from cracked faecal pellets was significantly higher than from intact pellets. Both contained viable seeds of all four cactus species, but particularly E. platyacanthus f. grandis.


Conclusions
Domestic goats are potential dispersers of the studied cactus species, although degradation of the faecal pellets is necessary to fully permit seedling emergence. These findings should be taken into account when designing management plans to conserve these endangered species.

This study analyzed the role of domestic goat as disperser of four endangered and endemic species of cacti. We analyzed the survival of seed after passage through the digestive tract of the goat and evaluated the capacity of viable seeds to germinate directly from fecal pellets. Our results show that domestic goat are potential dispersers of these species.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12015" xmlns="http://purl.org/rss/1.0/"><title>Pre-fire fuel reduction treatments influence plant communities and exotic species 9 years after a large wildfire</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12015</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Pre-fire fuel reduction treatments influence plant communities and exotic species 9 years after a large wildfire</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kristen L. Shive, Amanda M. Kuenzi, Carolyn H. Sieg, Peter Z. Fulé</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T10:59:15.853107-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12015</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12015</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12015</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12015-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How did post-wildfire understorey plant community response, including exotic species response, differ between pre-fire treated areas that were less severely burned, and pre-fire untreated areas that were more severely burned? Were these differences consistent through time?</p></div></div>
<div class="section" id="avsc12015-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>East-central Arizona, southwestern US.</p></div></div>
<div class="section" id="avsc12015-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We used a multi-year data set from the 2002 Rodeo–Chediski Fire to detect post-fire trends in plant community response in burned ponderosa pine forests. Within the burn perimeter, we examined the effects of pre-fire fuels treatments on post-fire vegetation by comparing paired treated and untreated sites on the Apache-Sitgreaves National Forest. We sampled these paired sites in 2004, 2005 and 2011.</p></div></div>
<div class="section" id="avsc12015-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>There were significant differences in pre-fire treated and untreated plant communities by species composition and abundance in 2004 and 2005, but these communities were beginning to converge in 2011. Total understorey plant cover was significantly higher in untreated areas for all 3 yr. Plant cover generally increased between 2004 and 2005 and markedly decreased in 2011, with the exception of shrub cover, which steadily increased through time. The sharp decrease in forb and graminoid cover in 2011 is likely related to drought conditions since the fire. Annual/biennial forb and graminoid cover decreased relative to perennial cover through time, consistent with the initial floristics hypothesis. Exotic plant response was highly variable and not limited to the immediate post-fire, annual/biennial community. Despite low overall exotic forb and graminoid cover for all years (&lt;2.5%), several exotic species increased in frequency, and the relative proportion of exotic to native cover increased through time.</p></div></div>
<div class="section" id="avsc12015-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Pre-treatment fuel reduction treatments helped maintain foundation overstorey species and associated native plant communities following this large wildfire. The overall low cover of exotic species on these sites supports other findings that the disturbance associated with high-severity fire does not always result in exotic species invasions. The increase in relative cover and frequency though time indicates that some species are proliferating, and continued monitoring is recommended. Patterns of exotic species invasions after severe burning are not easily predicted, and are likely more dependent on site-specific factors such as propagules, weather patterns and management.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12015/asset/image_m/avsc12015-toc-0001-m.png?v=1&amp;s=b48e196ba2447b2abc3a8e01fd0304540284368c" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12015/asset/image_n/avsc12015-toc-0001.gif?v=1&amp;s=2f93a18165deae35bcd5ff14bf83c9c7456a86c1"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Pre-wildfire fuels treatments in ponderosa pine forests had lasting effects on plant communities. Composition and abundance differed between treated and untreated areas initially, but began to converge 9 yr post-fire. Overall exotic species cover was &lt;2.5% for all years, but the frequency of several exotic species and the ratio of exotic to native cover increased in untreated areas over time.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How did post-wildfire understorey plant community response, including exotic species response, differ between pre-fire treated areas that were less severely burned, and pre-fire untreated areas that were more severely burned? Were these differences consistent through time?


Location
East-central Arizona, southwestern US.


Methods
We used a multi-year data set from the 2002 Rodeo–Chediski Fire to detect post-fire trends in plant community response in burned ponderosa pine forests. Within the burn perimeter, we examined the effects of pre-fire fuels treatments on post-fire vegetation by comparing paired treated and untreated sites on the Apache-Sitgreaves National Forest. We sampled these paired sites in 2004, 2005 and 2011.


Results
There were significant differences in pre-fire treated and untreated plant communities by species composition and abundance in 2004 and 2005, but these communities were beginning to converge in 2011. Total understorey plant cover was significantly higher in untreated areas for all 3 yr. Plant cover generally increased between 2004 and 2005 and markedly decreased in 2011, with the exception of shrub cover, which steadily increased through time. The sharp decrease in forb and graminoid cover in 2011 is likely related to drought conditions since the fire. Annual/biennial forb and graminoid cover decreased relative to perennial cover through time, consistent with the initial floristics hypothesis. Exotic plant response was highly variable and not limited to the immediate post-fire, annual/biennial community. Despite low overall exotic forb and graminoid cover for all years (&lt;2.5%), several exotic species increased in frequency, and the relative proportion of exotic to native cover increased through time.


Conclusions
Pre-treatment fuel reduction treatments helped maintain foundation overstorey species and associated native plant communities following this large wildfire. The overall low cover of exotic species on these sites supports other findings that the disturbance associated with high-severity fire does not always result in exotic species invasions. The increase in relative cover and frequency though time indicates that some species are proliferating, and continued monitoring is recommended. Patterns of exotic species invasions after severe burning are not easily predicted, and are likely more dependent on site-specific factors such as propagules, weather patterns and management.

Pre-wildfire fuels treatments in ponderosa pine forests had lasting effects on plant communities. Composition and abundance differed between treated and untreated areas initially, but began to converge 9 yr post-fire. Overall exotic species cover was &lt;2.5% for all years, but the frequency of several exotic species and the ratio of exotic to native cover increased in untreated areas over time.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12024" xmlns="http://purl.org/rss/1.0/"><title>Unmanned aerial vehicles as innovative remote sensing platforms for high-resolution infrared imagery to support restoration monitoring in cut-over bogs</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12024</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Unmanned aerial vehicles as innovative remote sensing platforms for high-resolution infrared imagery to support restoration monitoring in cut-over bogs</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christian Knoth, Birte Klein, Torsten Prinz, Till Kleinebecker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T08:40:32.0197-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12024</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12024</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12024</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12024-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Can UAV-based NIR remote sensing support restoration monitoring of cut-over bogs by providing valid information on species distribution and surface structure?</p></div></div>
<div class="section" id="avsc12024-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Restored polders of the Uchter Moor, a bog complex in NW Germany.</p></div></div>
<div class="section" id="avsc12024-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We used autonomously flying quadrocopters, supplied with either a panchromatic or colour infrared calibrated small frame digital camera to generate high resolution images of the restored bog surface. We performed a two-step classification process of automatic image segmentation and object-based classification to distinguish between four pre-defined classes (waterlogged bare peat, <em>Sphagnum</em> spp., <em>Eriophorum vaginatum</em> and <em>Betula pubescens</em>. An independent validation procedure was performed to evaluate the accuracy of the classification.</p></div></div>
<div class="section" id="avsc12024-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>A set-up composed of decision rules for reflectance, geometry and textural features was applied for identification of the four classes. The presented classification revealed an overall accuracy level of 91%. Most reliable attribution was obtained for waterlogged bare peat and <em>Sphagnum</em>-covered surfaces, revealing producer accuracies of 95% and 91%, respectively. Lower but still feasible accuracy levels were obtained for <em>Eriophorum vaginatum</em> and <em>Betula pubescens</em> individuals (89% and 84%, respectively).</p></div></div>
<div class="section" id="avsc12024-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>UAV-based NIR remote sensing is a promising tool for monitoring the restoration of cut-over bogs and has the potential to significantly reduce laborious field surveys. UAVs may increasingly play a significant role in future ecological monitoring studies, since they are small in size, highly flexible, easy to handle, non-emissive and available at a comparatively low cost.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12024/asset/image_m/avsc12024-toc-0001-m.png?v=1&amp;s=8d631cfbdea9befab499389092fca9003cccf0f1" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12024/asset/image_n/avsc12024-toc-0001.gif?v=1&amp;s=12631e808d762fbe2b2a34d1ff60b8dc5a14b2cf"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We tested whether high resolution images acquired with unmanned aerial vehicles (UAV) and modified digital cameras provide reliable information on species distribution and surface structure in a restored cut-over bog. The results document the high potential of UAV-based near infrared remote sensing techniques as a rapid and cost effective tool to support conservation and restoration monitoring of large peat bog areas.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Can UAV-based NIR remote sensing support restoration monitoring of cut-over bogs by providing valid information on species distribution and surface structure?


Location
Restored polders of the Uchter Moor, a bog complex in NW Germany.


Methods
We used autonomously flying quadrocopters, supplied with either a panchromatic or colour infrared calibrated small frame digital camera to generate high resolution images of the restored bog surface. We performed a two-step classification process of automatic image segmentation and object-based classification to distinguish between four pre-defined classes (waterlogged bare peat, Sphagnum spp., Eriophorum vaginatum and Betula pubescens. An independent validation procedure was performed to evaluate the accuracy of the classification.


Results
A set-up composed of decision rules for reflectance, geometry and textural features was applied for identification of the four classes. The presented classification revealed an overall accuracy level of 91%. Most reliable attribution was obtained for waterlogged bare peat and Sphagnum-covered surfaces, revealing producer accuracies of 95% and 91%, respectively. Lower but still feasible accuracy levels were obtained for Eriophorum vaginatum and Betula pubescens individuals (89% and 84%, respectively).


Conclusions
UAV-based NIR remote sensing is a promising tool for monitoring the restoration of cut-over bogs and has the potential to significantly reduce laborious field surveys. UAVs may increasingly play a significant role in future ecological monitoring studies, since they are small in size, highly flexible, easy to handle, non-emissive and available at a comparatively low cost.

We tested whether high resolution images acquired with unmanned aerial vehicles (UAV) and modified digital cameras provide reliable information on species distribution and surface structure in a restored cut-over bog. The results document the high potential of UAV-based near infrared remote sensing techniques as a rapid and cost effective tool to support conservation and restoration monitoring of large peat bog areas.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12020" xmlns="http://purl.org/rss/1.0/"><title>Cost-effective assessment of conservation status of fens</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12020</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cost-effective assessment of conservation status of fens</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dagmar K. Andersen, Bettina Nygaard, Jesper R. Fredshavn, Rasmus Ejrnæs</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-07T07:07:52.317059-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12020</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12020</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12020</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12020-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How can conservation status of rich fen and alkaline spring areas be assessed most cost-effectively based on existing monitoring data? What is the precision and accuracy of available indicators?</p></div></div>
<div class="section" id="avsc12020-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Rich fen and alkaline spring areas in Denmark.</p></div></div>
<div class="section" id="avsc12020-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Potential indicators of conservation status were evaluated based on: accuracy, measured as the ability to predict the number of typical species in monitoring plots; precision, measured as variation over years of indicators in repeated plots; and cost of obtaining data for the indicator. Indicators were derived using data from the Danish National Monitoring and Assessment Programme for the Aquatic and Terrestrial Environment from 2000 to 2009. Indicators included biotic indices derived from species lists, abiotic measurements of pH and nutrients and structural measurements of vegetation height and tree cover.</p></div></div>
<div class="section" id="avsc12020-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The majority of indicators showed a significant correlation with the number of typical species. Floristic indicators, especially based on Ellenberg nutrient values, showed superior correlation and were furthermore very stable over years. Structural indicators were generally accurate, but were highly imprecise with high between-year variation. Among the abiotic indicators, pH and soil P were inaccurate, whereas tissue N content and nitrate in water were accurate but with low precision. When balancing efficiency of indicators with monitoring costs, laboratory analyses stand out as expensive compared to recording of a species list, the latter providing up to five valuable indicators.</p></div></div>
<div class="section" id="avsc12020-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Floristic indicators derived from Ellenberg values, and especially those related to nutrient availability, are cost-effective indicators of conservation status. The method is applicable to all regions where Ellenberg indicator values have been calibrated to fit local conditions.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12020/asset/image_m/avsc12020-toc-0001-m.png?v=1&amp;s=af12f4541edb18f7a0a84e156333883cb829b256" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12020/asset/image_n/avsc12020-toc-0001.gif?v=1&amp;s=45c0da26eeb61c04d682d50d3006206900d29c37"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Different indicators of conservation status in rich fens and alkaline springs were evaluated based on accuracy (ability to predict number of typical species), precision (variation over years) and cost. We found that biotic indices based on Ellenberg indicator values, particularly the ratio between Ellenberg Nutrient and Ellenberg Reaction, outperformed chemical and structural indicators.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How can conservation status of rich fen and alkaline spring areas be assessed most cost-effectively based on existing monitoring data? What is the precision and accuracy of available indicators?


Location
Rich fen and alkaline spring areas in Denmark.


Methods
Potential indicators of conservation status were evaluated based on: accuracy, measured as the ability to predict the number of typical species in monitoring plots; precision, measured as variation over years of indicators in repeated plots; and cost of obtaining data for the indicator. Indicators were derived using data from the Danish National Monitoring and Assessment Programme for the Aquatic and Terrestrial Environment from 2000 to 2009. Indicators included biotic indices derived from species lists, abiotic measurements of pH and nutrients and structural measurements of vegetation height and tree cover.


Results
The majority of indicators showed a significant correlation with the number of typical species. Floristic indicators, especially based on Ellenberg nutrient values, showed superior correlation and were furthermore very stable over years. Structural indicators were generally accurate, but were highly imprecise with high between-year variation. Among the abiotic indicators, pH and soil P were inaccurate, whereas tissue N content and nitrate in water were accurate but with low precision. When balancing efficiency of indicators with monitoring costs, laboratory analyses stand out as expensive compared to recording of a species list, the latter providing up to five valuable indicators.


Conclusions
Floristic indicators derived from Ellenberg values, and especially those related to nutrient availability, are cost-effective indicators of conservation status. The method is applicable to all regions where Ellenberg indicator values have been calibrated to fit local conditions.

Different indicators of conservation status in rich fens and alkaline springs were evaluated based on accuracy (ability to predict number of typical species), precision (variation over years) and cost. We found that biotic indices based on Ellenberg indicator values, particularly the ratio between Ellenberg Nutrient and Ellenberg Reaction, outperformed chemical and structural indicators.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12023" xmlns="http://purl.org/rss/1.0/"><title>Effects of plant community composition and flowering phenology on honeybee foraging in Mediterranean sylvo-pastoral systems</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12023</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effects of plant community composition and flowering phenology on honeybee foraging in Mediterranean sylvo-pastoral systems</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Simonetta Bagella, Alberto Satta, Ignazio Floris, Maria Carmela Caria, Ivo Rossetti, János Podani</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-07T07:02:49.974494-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12023</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12023</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12023</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12023-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>Which are the most effective plant communities for honeybee foraging and honey production in Mediterranean sylvo-pastoral systems? What is the relationship between flowering phenology and pollen occurring in honey sediments?</p></div></div>
<div class="section" id="avsc12023-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Mediterranean sylvo-pastoral system in Gallura, Sardinia, Italy.</p></div></div>
<div class="section" id="avsc12023-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Phytosociological and phenological surveys were performed in a circular area of 1.5 km radius with a small apiary placed in the centre. Polleniferous and nectariferous values of plant communities were assessed based on the cover and the polleniferous and nectariferous value of each constituting species. Honey production was quantified during the main flow (March–June) and subjected to melissopalynological analysis. Data were evaluated by ordination through principal components analysis and principal coordinates analysis. The latter utilized a new index, developed for calculating the phenological distances based on the individual distributions of flowering frequencies.</p></div></div>
<div class="section" id="avsc12023-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Plant communities richest in species providing pollen and nectar were <em>Rhamnus</em> hedges. There was a close correlation between polleniferous and nectariferous values, suggesting that plant communities are important for honeybee foraging of both resources. The temporal flowering sequence ensured the supply of nectar and pollen throughout the spring season. Pollen foraged from 12 <em>Trifolium</em> species with different flowering phenology was the most abundant. <em>Salix purpurea</em> and <em>Rhamnus alaternus</em> were productive at the beginning of the season, followed by <em>Lavandula stoechas</em>,<em> Echium plantagineum</em> and <em>E. italicum</em>.</p></div></div>
<div class="section" id="avsc12023-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Plant communities vary in importance for honeybee foraging mainly due to differences in floristic composition and flowering phenology. Communities characterized by human presence (e.g. semi-natural grasslands and hedges) are the most relevant. Some target species (e.g. <em>Trifolium</em> spp.) favoured by grazing livestock ensure foraging for honeybees throughout the season. Plant communities of wild areas, such as the garrigue vegetation, provide foraging for unifloral valuable honey (i.e. ‘<em>Lavandula</em>’ honey).</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12023/asset/image_m/avsc12023-toc-0001-m.png?v=1&amp;s=8ed35aaa2aa1f44f06a7c44864b20755de3c7e29" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12023/asset/image_n/avsc12023-toc-0001.gif?v=1&amp;s=6d8b648f5d40fe6c17df233021800cf8d9315faf"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Plant communities vary in importance for honeybee foraging mainly due to differences in floristic composition and flowering phenology. Communities characterized by human presence are the most relevant. Some target species favoured by grazing livestock ensure foraging for honeybees throughout the season. Plant communities of wild areas, such as the garrigue vegetation, provide foraging for unifloral valuable honey.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
Which are the most effective plant communities for honeybee foraging and honey production in Mediterranean sylvo-pastoral systems? What is the relationship between flowering phenology and pollen occurring in honey sediments?


Location
Mediterranean sylvo-pastoral system in Gallura, Sardinia, Italy.


Methods
Phytosociological and phenological surveys were performed in a circular area of 1.5 km radius with a small apiary placed in the centre. Polleniferous and nectariferous values of plant communities were assessed based on the cover and the polleniferous and nectariferous value of each constituting species. Honey production was quantified during the main flow (March–June) and subjected to melissopalynological analysis. Data were evaluated by ordination through principal components analysis and principal coordinates analysis. The latter utilized a new index, developed for calculating the phenological distances based on the individual distributions of flowering frequencies.


Results
Plant communities richest in species providing pollen and nectar were Rhamnus hedges. There was a close correlation between polleniferous and nectariferous values, suggesting that plant communities are important for honeybee foraging of both resources. The temporal flowering sequence ensured the supply of nectar and pollen throughout the spring season. Pollen foraged from 12 Trifolium species with different flowering phenology was the most abundant. Salix purpurea and Rhamnus alaternus were productive at the beginning of the season, followed by Lavandula stoechas, Echium plantagineum and E. italicum.


Conclusions
Plant communities vary in importance for honeybee foraging mainly due to differences in floristic composition and flowering phenology. Communities characterized by human presence (e.g. semi-natural grasslands and hedges) are the most relevant. Some target species (e.g. Trifolium spp.) favoured by grazing livestock ensure foraging for honeybees throughout the season. Plant communities of wild areas, such as the garrigue vegetation, provide foraging for unifloral valuable honey (i.e. ‘Lavandula’ honey).

Plant communities vary in importance for honeybee foraging mainly due to differences in floristic composition and flowering phenology. Communities characterized by human presence are the most relevant. Some target species favoured by grazing livestock ensure foraging for honeybees throughout the season. Plant communities of wild areas, such as the garrigue vegetation, provide foraging for unifloral valuable honey.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12018" xmlns="http://purl.org/rss/1.0/"><title>Effect of geomorphology and nitrogen deposition on rate of vegetation succession in inland drift sands</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12018</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effect of geomorphology and nitrogen deposition on rate of vegetation succession in inland drift sands</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laurens B. Sparrius, Annemieke M. Kooijman, Michel P.J.M. Riksen, Jan Sevink</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-28T04:41:55.71592-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12018</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12018</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12018</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12018-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>(1) At what rate does succession take place in active and more stabilized drift sands in regions with low and high N deposition in the Netherlands? (2) What is the present composition of pioneer vegetation in active and more stabilized drift sands in regions with low and high N deposition? (3) What efforts are necessary to conserve bare sand in drift sands?</p></div></div>
<div class="section" id="avsc12018-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Eight inland dunes in the Netherlands, which represent four active and four more stabilized drift sands in regions with low and high N deposition.</p></div></div>
<div class="section" id="avsc12018-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Aerial photographs from 1950, 1981, 1995 and 2007 were used to compare rates of succession from bare sand towards forest. For each site, a detailed vegetation map was made in 2007.</p></div></div>
<div class="section" id="avsc12018-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>In all studied sites, bare sand decreased, especially in regions with high N deposition. This decline was significantly higher between 1981 and 2007 than between 1950 and 1981. The loss of bare sand did not lead to an increase of pioneer vegetation, which remained more or less stable; it led, however, to an increase of heath and forest. In active drift sands, pioneer vegetation was characterized by <em>Corynephorus canescens</em> and <em>Polytrichum piliferum</em>, while lichens, lichen-rich grassland and <em>Campylopus introflexus</em> were more common in stabilized drift sands. In regions with high N deposition, the proportion of <em>Campylopus introflexus</em> to older pioneer stages was significantly higher, and the contribution of forest to the ‘heath/forest’ vegetation class was also higher. The calculated life span of bare sand decreased in all sites. Extrapolation of the results suggests that in the absence of restoration measures, bare sand will vanish by 2035.</p></div></div>
<div class="section" id="avsc12018-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>In both active and more stabilized drift sands, a generic loss of bare sand and an increase in forest area was found. The increase was higher in regions with high N deposition. Conservation management should include the annual transformation of 43 ha of forest into bare sand in order to stop the loss of bare sand.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12018/asset/image_m/avsc12018-toc-0001-m.png?v=1&amp;s=8c767bf7bf6e37b07db6da1a4d1ae332e5da0007" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12018/asset/image_n/avsc12018-toc-0001.gif?v=1&amp;s=f27719feb0023b9f259c68575c601751d2ba53bd"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In eight larger inland dune reserves in the Netherlands, half of the bare sand area became covered in vegetation between 1950 and 2007. The decline of this semi-natural habitat is still going on. Apart from a generic increase in cover, terrain topology and nitrogen deposition where found to be important factors explaining the current vegetation.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
(1) At what rate does succession take place in active and more stabilized drift sands in regions with low and high N deposition in the Netherlands? (2) What is the present composition of pioneer vegetation in active and more stabilized drift sands in regions with low and high N deposition? (3) What efforts are necessary to conserve bare sand in drift sands?


Location
Eight inland dunes in the Netherlands, which represent four active and four more stabilized drift sands in regions with low and high N deposition.


Methods
Aerial photographs from 1950, 1981, 1995 and 2007 were used to compare rates of succession from bare sand towards forest. For each site, a detailed vegetation map was made in 2007.


Results
In all studied sites, bare sand decreased, especially in regions with high N deposition. This decline was significantly higher between 1981 and 2007 than between 1950 and 1981. The loss of bare sand did not lead to an increase of pioneer vegetation, which remained more or less stable; it led, however, to an increase of heath and forest. In active drift sands, pioneer vegetation was characterized by Corynephorus canescens and Polytrichum piliferum, while lichens, lichen-rich grassland and Campylopus introflexus were more common in stabilized drift sands. In regions with high N deposition, the proportion of Campylopus introflexus to older pioneer stages was significantly higher, and the contribution of forest to the ‘heath/forest’ vegetation class was also higher. The calculated life span of bare sand decreased in all sites. Extrapolation of the results suggests that in the absence of restoration measures, bare sand will vanish by 2035.


Conclusions
In both active and more stabilized drift sands, a generic loss of bare sand and an increase in forest area was found. The increase was higher in regions with high N deposition. Conservation management should include the annual transformation of 43 ha of forest into bare sand in order to stop the loss of bare sand.

In eight larger inland dune reserves in the Netherlands, half of the bare sand area became covered in vegetation between 1950 and 2007. The decline of this semi-natural habitat is still going on. Apart from a generic increase in cover, terrain topology and nitrogen deposition where found to be important factors explaining the current vegetation.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12017" xmlns="http://purl.org/rss/1.0/"><title>Vegetation diversity of salt-rich grasslands in Southeast Europe</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12017</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Vegetation diversity of salt-rich grasslands in Southeast Europe</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pavol Eliáš, Desislava Sopotlieva, Daniel Dítě, Petra Hájková, Iva Apostolova, Dušan Senko, Zuzana Melečková, Michal Hájek</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-27T03:49:37.889306-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12017</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12017</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12017</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Special Feature: Grassland Classification</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12017-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>How does the plant species composition of Pontic–Pannonian salt-rich habitats vary on a large geographical scale? Do the floristic differences between Pannonia and the Balkans correspond to the current phytosociological classification?</p></div></div>
<div class="section" id="avsc12017-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Pannonia (Hungary, Slovakia, Austria, Czech Republic, Croatia, Serbia, Romania) and the Balkans (Bulgaria, Macedonia, Greece).</p></div></div>
<div class="section" id="avsc12017-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Two thousand four hundred and thirty-seven relevés from halophytic and sub-halophytic habitats were classified using a modified TWINSPAN. The crispness of classification was checked. DCA and CCA with climate data as explanatory variables were applied.</p></div></div>
<div class="section" id="avsc12017-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The classification was best interpreted at the level of 15 clusters. The vegetation changed along the salinity gradient from sub-halophytic grasslands (including <em>Trifolion resupinati</em> alliance of the <em>Molinio-Arrhenatheretalia</em> class and <em>Beckmannion eruciformis</em> and <em>Festucion pseudovinae</em> p. p. alliances of the <em>Festuco-Puccinellietea</em> class) and reed beds (<em>Bolboschoenion maritimi</em> p. p. alliance; the <em>Phragmito-Magnocaricetea</em> class), through steppe and wet inland halophytic vegetation (<em>Festucion pseudovinae</em> p. p.<em>, Puccinellion limosae, Pucinellion convolutae, Bolboschoenion maritimi</em> p. p. and <em>Juncion gerardii</em> of the <em>Festuco-Puccinellietea</em> class) towards the extreme halophytic vegetation of the <em>Thero-Salicornietea, Crypsietea</em> and <em>Juncetea maritimi</em> classes. This gradient was longer in the Balkan region, where it spanned from the sub-mediterranean salt-rich grasslands to the extremely halophytic vegetation at the Black Sea coast. The second most important gradient coincided with the water regime. Some vegetation types appeared to be confined to either the Pannonian or the Balkan region (especially within dry sub-halophytic and steppe halophytic grasslands), while others were distributed across the entire study area. The above-mentioned pattern did not always correspond with current classification systems.</p></div></div>
<div class="section" id="avsc12017-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Variation in salt-rich vegetation predominantly follows the salinity and water regime gradients. Geographical variation, generally coinciding with climatic and historical effects, is also important, especially in drier salt-rich habitats. Our large-scale analysis of the floristic variation of salt-rich habitats might be useful for the unification of classification systems that differ substantially between the countries involved. In addition, the analysis may be useful for adjustment of a classification system in the poorly explored Balkan region, where particular vegetation types were identified with, or delimited from, Central European vegetation types without detailed comparative analysis until now.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12017/asset/image_m/avsc12017-toc-0001-m.png?v=1&amp;s=adf16e544c8d6ee4ca46ceaf563fbd29736a11a6" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12017/asset/image_n/avsc12017-toc-0001.gif?v=1&amp;s=e6c6d01a7a370d245c1ef9b442da22a77dbc4156"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In order to find how the plant species composition of Pontic–Pannonian salt-rich habitats varies on a large geographical scale and whether floristic differences between Pannonian and Balkan regions correspond to phytosociological classification, we classified 2437 relevés from halophytic and sub-halophytic habitats from the Pannonian–Balkan region spanning ten European countries. A syntaxonomic synopsis is presented for this region.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
How does the plant species composition of Pontic–Pannonian salt-rich habitats vary on a large geographical scale? Do the floristic differences between Pannonia and the Balkans correspond to the current phytosociological classification?


Location
Pannonia (Hungary, Slovakia, Austria, Czech Republic, Croatia, Serbia, Romania) and the Balkans (Bulgaria, Macedonia, Greece).


Methods
Two thousand four hundred and thirty-seven relevés from halophytic and sub-halophytic habitats were classified using a modified TWINSPAN. The crispness of classification was checked. DCA and CCA with climate data as explanatory variables were applied.


Results
The classification was best interpreted at the level of 15 clusters. The vegetation changed along the salinity gradient from sub-halophytic grasslands (including Trifolion resupinati alliance of the Molinio-Arrhenatheretalia class and Beckmannion eruciformis and Festucion pseudovinae p. p. alliances of the Festuco-Puccinellietea class) and reed beds (Bolboschoenion maritimi p. p. alliance; the Phragmito-Magnocaricetea class), through steppe and wet inland halophytic vegetation (Festucion pseudovinae p. p., Puccinellion limosae, Pucinellion convolutae, Bolboschoenion maritimi p. p. and Juncion gerardii of the Festuco-Puccinellietea class) towards the extreme halophytic vegetation of the Thero-Salicornietea, Crypsietea and Juncetea maritimi classes. This gradient was longer in the Balkan region, where it spanned from the sub-mediterranean salt-rich grasslands to the extremely halophytic vegetation at the Black Sea coast. The second most important gradient coincided with the water regime. Some vegetation types appeared to be confined to either the Pannonian or the Balkan region (especially within dry sub-halophytic and steppe halophytic grasslands), while others were distributed across the entire study area. The above-mentioned pattern did not always correspond with current classification systems.


Conclusions
Variation in salt-rich vegetation predominantly follows the salinity and water regime gradients. Geographical variation, generally coinciding with climatic and historical effects, is also important, especially in drier salt-rich habitats. Our large-scale analysis of the floristic variation of salt-rich habitats might be useful for the unification of classification systems that differ substantially between the countries involved. In addition, the analysis may be useful for adjustment of a classification system in the poorly explored Balkan region, where particular vegetation types were identified with, or delimited from, Central European vegetation types without detailed comparative analysis until now.

In order to find how the plant species composition of Pontic–Pannonian salt-rich habitats varies on a large geographical scale and whether floristic differences between Pannonian and Balkan regions correspond to phytosociological classification, we classified 2437 relevés from halophytic and sub-halophytic habitats from the Pannonian–Balkan region spanning ten European countries. A syntaxonomic synopsis is presented for this region.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12021" xmlns="http://purl.org/rss/1.0/"><title>Drivers of beta-diversity variation in Bromus erectus semi-natural dry grasslands</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12021</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Drivers of beta-diversity variation in Bromus erectus semi-natural dry grasslands</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sabina Burrascano, Ilaria Anzellotti, Emanuela Carli, Eva Del Vico, Laura Facioni, Francesca Pretto, Francesco M. Sabatini, Agnese Tilia, Carlo Blasi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-26T06:35:53.691265-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12021</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12021</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12021</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12021-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>What are the main drivers of variation in beta-diversity for <em>Bromus erectus</em> semi-natural dry grasslands of habitat 6210(*) at different scales? How should environmental variables and spatial patterns be taken into account to conserve the maximum possible beta-diversity within the habitat?</p></div></div>
<div class="section" id="avsc12021-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Central Italy.</p></div></div>
<div class="section" id="avsc12021-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We used 195 vegetation relevés distributed in three nested extents: a single mountain, a mountain chain and southern Lazio. Multiple regression on distance matrices was performed using dissimilarity matrices based on: (1) species abundances as response variables; (2) spatial coordinates and environmental parameters (altitude, slope, percentage of rock and stone coverage, aspect, annual rainfall) as explanatory variables. The two groups of explanatory variables were used separately to partition the variation, and jointly to assess the relative contribution of each individual variable. Those variables found to significantly affect beta-diversity were used to: (1) compare beta-diversity levels between a set of randomly selected and a set of stratified relevés; and (2) analyse the habitat distribution across environmental gradients. These analyses, together with the curves describing the relationships between spatial distances and composition dissimilarities, were used to inform management decisions for the habitat.</p></div></div>
<div class="section" id="avsc12021-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Most of the variance was explained by environmental variables, whose share was higher in the smallest and intermediate extent than in the broadest extent. Community dissimilarity increased in proportion to differences in altitude and spatial distances at every extent. Accordingly, at all the extents, the selection of relevés stratified by altitude or selected taking into account a minimum spatial distance included significantly higher levels of within-habitat beta-diversity, than randomly selected relevés. The relation of beta-diversity to the variation in aspect and annual rainfall varied at different extents.</p></div></div>
<div class="section" id="avsc12021-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Our results demonstrate that dry grassland management plans aimed at conserving the maximum within-habitat beta-diversity should take into account variation in environmental variables, among which altitude proved to be a critical factor at every extent. Also, spatial distances positively affect within-habitat beta-diversity levels, and scale-dependent minimum distances among habitat patches should be taken into account when selecting patches of habitat 6210(*) to be conserved in the study area.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12021/asset/image_m/avsc12021-toc-0001-m.png?v=1&amp;s=125b15e14b8ecfcfe4c57dd12ef82072464ab8ee" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12021/asset/image_n/avsc12021-toc-0001.gif?v=1&amp;s=0604e1d59dad280a5a1e4edf41bf4e1f561b39f8"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We identified the drivers of variation in dry grasslands β-diversity at multiple scales to help managers define conservation priorities. Our results demonstrate that environmental variables, especially altitude, are critical factors affecting the within-habitat β-diversity levels. Moreover scale-dependent minimum distances among habitat patches should be taken into account when selecting grasslands patches to be conserved.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
What are the main drivers of variation in beta-diversity for Bromus erectus semi-natural dry grasslands of habitat 6210(*) at different scales? How should environmental variables and spatial patterns be taken into account to conserve the maximum possible beta-diversity within the habitat?


Location
Central Italy.


Methods
We used 195 vegetation relevés distributed in three nested extents: a single mountain, a mountain chain and southern Lazio. Multiple regression on distance matrices was performed using dissimilarity matrices based on: (1) species abundances as response variables; (2) spatial coordinates and environmental parameters (altitude, slope, percentage of rock and stone coverage, aspect, annual rainfall) as explanatory variables. The two groups of explanatory variables were used separately to partition the variation, and jointly to assess the relative contribution of each individual variable. Those variables found to significantly affect beta-diversity were used to: (1) compare beta-diversity levels between a set of randomly selected and a set of stratified relevés; and (2) analyse the habitat distribution across environmental gradients. These analyses, together with the curves describing the relationships between spatial distances and composition dissimilarities, were used to inform management decisions for the habitat.


Results
Most of the variance was explained by environmental variables, whose share was higher in the smallest and intermediate extent than in the broadest extent. Community dissimilarity increased in proportion to differences in altitude and spatial distances at every extent. Accordingly, at all the extents, the selection of relevés stratified by altitude or selected taking into account a minimum spatial distance included significantly higher levels of within-habitat beta-diversity, than randomly selected relevés. The relation of beta-diversity to the variation in aspect and annual rainfall varied at different extents.


Conclusions
Our results demonstrate that dry grassland management plans aimed at conserving the maximum within-habitat beta-diversity should take into account variation in environmental variables, among which altitude proved to be a critical factor at every extent. Also, spatial distances positively affect within-habitat beta-diversity levels, and scale-dependent minimum distances among habitat patches should be taken into account when selecting patches of habitat 6210(*) to be conserved in the study area.

We identified the drivers of variation in dry grasslands β-diversity at multiple scales to help managers define conservation priorities. Our results demonstrate that environmental variables, especially altitude, are critical factors affecting the within-habitat β-diversity levels. Moreover scale-dependent minimum distances among habitat patches should be taken into account when selecting grasslands patches to be conserved.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12019" xmlns="http://purl.org/rss/1.0/"><title>Influence of forest road, road-surfacing material and stand age on floristic diversity and composition in a nutrient-poor environment</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12019</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Influence of forest road, road-surfacing material and stand age on floristic diversity and composition in a nutrient-poor environment</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laurent Bergès, Richard Chevalier, Catherine Avon</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-21T02:09:20.699871-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12019</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12019</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12019</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12019-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How did the presence of forest roads modify plant diversity and composition in a nutrient-poor environment? What was the effect of the use of limestone gravel as road surfacing material? How did floristic succession vary between roadside and forest interior?</p></div></div>
<div class="section" id="avsc12019-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>State Forest of Orléans, Loiret, northern France.</p></div></div>
<div class="section" id="avsc12019-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We sampled 30 pairs of 2000-m<sup>2</sup> plots, one on a road and the other 30 m inside the forest, on two road surfacing materials (limestone gravel and bare soil) and three stand ages (young, middle-aged and mature) in Scots and Corsican pine stands in a large managed forest. Plant diversity was analysed according to life-history traits (protection status, indigenousness, life form, habitat and ecological preferences). We tested the effects of plot position, road type and stand age on species richness, species composition and individual species response.</p></div></div>
<div class="section" id="avsc12019-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The species richness of all plant groups was always higher on roads compared to forest stands, and the forest plot communities were nearly completely nested within the roadside plot communities. Seven protected species and four non-native potentially invasive species were observed on roadsides. Limestone-gravelled roads hosted more species than bare soil roads, but acidophilous forest and grassland species richness was higher on bare soil roads. Plant composition similarity between the roadside and forest were higher at early successional stages and lower in older stages.</p></div></div>
<div class="section" id="avsc12019-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Roads have inseparable positive and negative effects on plant communities, but the negative ones are of great concern. To prevent further damage in these nutrient-poor ecosystems, we recommend monitoring road sections hosting protected acidophilous species, not increasing road density, and replacing limestone gravel with a low pH endogenous material.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12019/asset/image_m/avsc12019-toc-0001-m.png?v=1&amp;s=717c1594147cc0a684f7e349e6c9697d887a838e" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12019/asset/image_n/avsc12019-toc-0001.gif?v=1&amp;s=91faeaa2f4f1b555c19768f6501c4be8dcfe92df"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We compared vegetation on limestone-gravelled and bare soil forest roads in a large forest on acidic soils. We found that roads have inseparable positive and negative effects on plant communities. To prevent further damage in these nutrient-poor ecosystems, we recommend monitoring road sections hosting protected acidophilous species, not increasing road density, and replacing limestone gravel by a low-pH endogenous material.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How did the presence of forest roads modify plant diversity and composition in a nutrient-poor environment? What was the effect of the use of limestone gravel as road surfacing material? How did floristic succession vary between roadside and forest interior?


Location
State Forest of Orléans, Loiret, northern France.


Methods
We sampled 30 pairs of 2000-m2 plots, one on a road and the other 30 m inside the forest, on two road surfacing materials (limestone gravel and bare soil) and three stand ages (young, middle-aged and mature) in Scots and Corsican pine stands in a large managed forest. Plant diversity was analysed according to life-history traits (protection status, indigenousness, life form, habitat and ecological preferences). We tested the effects of plot position, road type and stand age on species richness, species composition and individual species response.


Results
The species richness of all plant groups was always higher on roads compared to forest stands, and the forest plot communities were nearly completely nested within the roadside plot communities. Seven protected species and four non-native potentially invasive species were observed on roadsides. Limestone-gravelled roads hosted more species than bare soil roads, but acidophilous forest and grassland species richness was higher on bare soil roads. Plant composition similarity between the roadside and forest were higher at early successional stages and lower in older stages.


Conclusions
Roads have inseparable positive and negative effects on plant communities, but the negative ones are of great concern. To prevent further damage in these nutrient-poor ecosystems, we recommend monitoring road sections hosting protected acidophilous species, not increasing road density, and replacing limestone gravel with a low pH endogenous material.

We compared vegetation on limestone-gravelled and bare soil forest roads in a large forest on acidic soils. We found that roads have inseparable positive and negative effects on plant communities. To prevent further damage in these nutrient-poor ecosystems, we recommend monitoring road sections hosting protected acidophilous species, not increasing road density, and replacing limestone gravel by a low-pH endogenous material.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12016" xmlns="http://purl.org/rss/1.0/"><title>Grassland afforestation impact on primary productivity: a remote sensing approach</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12016</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Grassland afforestation impact on primary productivity: a remote sensing approach</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Mercedes Vassallo, Hernán D. Dieguez, Martín F. Garbulsky, Esteban G. Jobbágy, José M. Paruelo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-20T00:45:47.098505-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12016</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12016</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12016</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12016-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>How is the magnitude and seasonality of carbon uptake affected by the replacement of native grasslands by eucalyptus plantations?</p></div></div>
<div class="section" id="avsc12016-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Río de la Plata Grasslands in Argentina and Uruguay.</p></div></div>
<div class="section" id="avsc12016-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>A total of 115 paired sites of fast-growing <em>Eucalyptus grandis</em> plantations and adjacent grasslands were used to characterize the magnitude and seasonality of (1) radiation interception by canopies and (2) above-ground net primary productivity based on a time series of MODIS-derived normalized difference vegetation index (NDVI). The response of NDVI to precipitation was explored across temporal scales.</p></div></div>
<div class="section" id="avsc12016-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>NDVI in afforested vs. grassland plots presented higher annual averages (1.3-fold), lower seasonal ranges (average relative range of 0.11 vs. 0.29) and delayed growing seasons (2-month shift). Temporally, NDVI was positively associated with precipitation input, showing a correlation with longer periods of precipitation accumulation in tree plantations compared to grasslands (&gt; 7 vs. 2–3 months). Estimated average annual above-ground net primary productivity (ANPP) almost quadrupled as a consequence of replacing grasslands by tree plantations (∼4 vs. ∼17 Mg dry matter. ha<sup>−1·</sup>yr<sup>−1</sup>), and this difference was evidenced throughout the whole study period.</p></div></div>
<div class="section" id="avsc12016-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Afforested grasslands intercept more radiation and have higher and more stable ANPP throughout the year, probably as a result of major changes in leaf phenology and root distribution patterns, which in turn allowed better access to water. Changes in carbon uptake can influence climate/biosphere feedbacks and should be considered in land-use planning, especially when grassland afforestation is recommended as a tool to mitigate global warming.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12016/asset/image_m/avsc12016-toc-0001-m.png?v=1&amp;s=949502638554871c2d1c85274f125a831f24bafc" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12016/asset/image_n/avsc12016-toc-0001.gif?v=1&amp;s=aadd922918d947e1a712a39ea67198bfeb412732"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Afforestation represents a dramatic structural and functional change when hosted by tree-less ecosystems. We showed that afforested plots in Río de la Plata Grasslands presented a delay in growing season, intercepted more radiation and had a higher and more stable primary productivity throughout the year. Furthermore tree plantations were more sensitive to past precipitation than grasslands.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
How is the magnitude and seasonality of carbon uptake affected by the replacement of native grasslands by eucalyptus plantations?


Location
Río de la Plata Grasslands in Argentina and Uruguay.


Methods
A total of 115 paired sites of fast-growing Eucalyptus grandis plantations and adjacent grasslands were used to characterize the magnitude and seasonality of (1) radiation interception by canopies and (2) above-ground net primary productivity based on a time series of MODIS-derived normalized difference vegetation index (NDVI). The response of NDVI to precipitation was explored across temporal scales.


Results
NDVI in afforested vs. grassland plots presented higher annual averages (1.3-fold), lower seasonal ranges (average relative range of 0.11 vs. 0.29) and delayed growing seasons (2-month shift). Temporally, NDVI was positively associated with precipitation input, showing a correlation with longer periods of precipitation accumulation in tree plantations compared to grasslands (&gt; 7 vs. 2–3 months). Estimated average annual above-ground net primary productivity (ANPP) almost quadrupled as a consequence of replacing grasslands by tree plantations (∼4 vs. ∼17 Mg dry matter. ha−1·yr−1), and this difference was evidenced throughout the whole study period.


Conclusions
Afforested grasslands intercept more radiation and have higher and more stable ANPP throughout the year, probably as a result of major changes in leaf phenology and root distribution patterns, which in turn allowed better access to water. Changes in carbon uptake can influence climate/biosphere feedbacks and should be considered in land-use planning, especially when grassland afforestation is recommended as a tool to mitigate global warming.

Afforestation represents a dramatic structural and functional change when hosted by tree-less ecosystems. We showed that afforested plots in Río de la Plata Grasslands presented a delay in growing season, intercepted more radiation and had a higher and more stable primary productivity throughout the year. Furthermore tree plantations were more sensitive to past precipitation than grasslands.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12009" xmlns="http://purl.org/rss/1.0/"><title>Fragment size, vegetation structure and physical environment control grassland functioning: a test based on artificial neural networks</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12009</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fragment size, vegetation structure and physical environment control grassland functioning: a test based on artificial neural networks</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lorena P. Herrera, M. Texeira, J.M. Paruelo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-11T06:28:23.828554-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12009</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12009</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12009</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12009-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How do fragment-level characteristics affect remnant grassland functioning in a highly transformed landscape? Are artificial neural networks (ANNs) a better statistical tool to model variations in grassland functioning compared to linear regression models (LRMs)?</p></div></div>
<div class="section" id="avsc12009-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Tandilia Range, Southern Pampa, Buenos Aires Province, Argentina.</p></div></div>
<div class="section" id="avsc12009-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We characterized the dynamics of the vegetation functioning in 60 remnant grasslands using enhanced vegetation index (EVI) data provided by MODIS/Terra images from July 2000 to June 2005. First, we performed a principal components analysis (PCA) on the fragment mean monthly values of EVI in order to obtain synthetic measures (i.e. the PCA axes) of grassland functioning. Grassland fragments were also characterized by size, vegetation structure (abundance of the tall-tussock grass <em>Paspalum quadrifarium</em>) and physical environment (soil type – abundance of litholitic soils – elevation, aspect and slope). The relationship between grassland functioning and these explanatory variables was explored using linear regression models (LRMs) and artificial neural networks (ANNs).</p></div></div>
<div class="section" id="avsc12009-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The first and second PCA axes were related to the annual integral of EVI (EVI-I) and EVI seasonality (EVI-S), respectively; these explained jointly ca. 80% of total variability in mean EVI values. ANNs captured better than regression models the relationships among the proposed controls and the spatial variability of grassland functioning in Southern Pampa. Results showed that EVI-I variability was related to all independent variables except aspect. While fragment size, litholitic soils and slope were negatively related to EVI-I, the abundance of <em>P. quadrifarium</em> had a positive effect on the spectral index. Grasslands with high seasonality were large and had high slope and aspect, low abundance of <em>P. quadrifarium</em> and increased abundance of litholitic soils.</p></div></div>
<div class="section" id="avsc12009-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Our results showed that grassland functioning in Southern Pampa, as estimated by EVI, depends on fragment size, vegetation structure and physical factors (soil type, aspect and slope). <em>Paspalum quadrifarium</em> may have an important functional role in this grassland system.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12009/asset/image_m/avsc12009-toc-0001-m.png?v=1&amp;s=5c153e6a3d96ef84dbedfc34f816bc2d582cf9a6" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12009/asset/image_n/avsc12009-toc-0001.gif?v=1&amp;s=b42914b8399e6b0eacc288a8ca6266a4f6f0d575"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Through artificial neural networks we showed that the temporal dynamics of remnant grasslands in Southern Pampa (Argentina) is controlled by the size of fragments, the vegetation structure (abundance of native grass <em>Paspalum quadrifarium</em>) … and the physical environment? (soil, aspect and slope). We highlight the importance of landscape structure as a key control of ecosystem functioning, an aspect seldom considered in the literature.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How do fragment-level characteristics affect remnant grassland functioning in a highly transformed landscape? Are artificial neural networks (ANNs) a better statistical tool to model variations in grassland functioning compared to linear regression models (LRMs)?


Location
Tandilia Range, Southern Pampa, Buenos Aires Province, Argentina.


Methods
We characterized the dynamics of the vegetation functioning in 60 remnant grasslands using enhanced vegetation index (EVI) data provided by MODIS/Terra images from July 2000 to June 2005. First, we performed a principal components analysis (PCA) on the fragment mean monthly values of EVI in order to obtain synthetic measures (i.e. the PCA axes) of grassland functioning. Grassland fragments were also characterized by size, vegetation structure (abundance of the tall-tussock grass Paspalum quadrifarium) and physical environment (soil type – abundance of litholitic soils – elevation, aspect and slope). The relationship between grassland functioning and these explanatory variables was explored using linear regression models (LRMs) and artificial neural networks (ANNs).


Results
The first and second PCA axes were related to the annual integral of EVI (EVI-I) and EVI seasonality (EVI-S), respectively; these explained jointly ca. 80% of total variability in mean EVI values. ANNs captured better than regression models the relationships among the proposed controls and the spatial variability of grassland functioning in Southern Pampa. Results showed that EVI-I variability was related to all independent variables except aspect. While fragment size, litholitic soils and slope were negatively related to EVI-I, the abundance of P. quadrifarium had a positive effect on the spectral index. Grasslands with high seasonality were large and had high slope and aspect, low abundance of P. quadrifarium and increased abundance of litholitic soils.


Conclusions
Our results showed that grassland functioning in Southern Pampa, as estimated by EVI, depends on fragment size, vegetation structure and physical factors (soil type, aspect and slope). Paspalum quadrifarium may have an important functional role in this grassland system.

Through artificial neural networks we showed that the temporal dynamics of remnant grasslands in Southern Pampa (Argentina) is controlled by the size of fragments, the vegetation structure (abundance of native grass Paspalum quadrifarium) … and the physical environment? (soil, aspect and slope). We highlight the importance of landscape structure as a key control of ecosystem functioning, an aspect seldom considered in the literature.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12013" xmlns="http://purl.org/rss/1.0/"><title>Disturbance and recovery in semi-arid Mediterranean grasslands</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12013</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Disturbance and recovery in semi-arid Mediterranean grasslands</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Theodora P. Merou, Spyros Tsiftsis, Vasilios P. Papanastasis</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-04T04:16:31.543224-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12013</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12013</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12013</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12013-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Aims</h4><div class="para"><p>(1) To investigate the temporal response of semi-arid Mediterranean grasslands to multiple disturbances as well as P fertilization and irrigation; and (2) to determine the reaction of single species or groups of species as well as the extent of recovery of the grassland community following cessation of the above interventions.</p></div></div>
<div class="section" id="avsc12013-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>North Greece.</p></div></div>
<div class="section" id="avsc12013-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>In a fenced area, six treatments (burning, irrigation, digging, cutting, P fertilization and control) were applied, for three growing seasons, in a completely randomized block design with four blocks. Biomass was sampled in five (0.5 × 0.5 m) quadrats per plot at the end of the growing season and sorted into the following functional groups: annual grasses, perennial grasses, annual legumes and forbs (that included all the other species). Measurements were repeated 1 and 7 yr after cessation of the treatments.</p></div></div>
<div class="section" id="avsc12013-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Annual grasses and legumes were positively favoured by cutting, burning and digging, which produced changes in vegetation composition over time. P fertilization had a positive influence on total legume biomass. Effects on individual species were not uniform. Plant composition after cessation of the disturbance treatments was quite different. Total legume biomass remained high 1 yr after the cessation of P fertilization but declined thereafter. Annual grasses and legumes constituted the largest portion of the total biomass in the first year of the experiment. Disturbance (burning, cutting and digging) gradually reduced their biomass in favour of forbs. Seven years after cessation of the treatments, the tall annual, as well as perennial grasses constituted more than 80% of the total biomass. Under conditions of disturbance, short annual species had an advantage over perennials, while cessation of disturbance enables perennial grasses to dominate.</p></div></div>
<div class="section" id="avsc12013-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Disturbance promotes the dominance of annuals, especially species with a persistent seed bank. Repeated disturbance encourages an increase of small or prostrate species. Cessation of disturbance leads to the rapid recovery of biomass production. Tall annuals are promoted. P fertilization clearly favours legumes in the short term.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12013/asset/image_m/avsc12013-toc-0001-m.png?v=1&amp;s=2012117d708ac8664831d2658dce85f92998f90c" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12013/asset/image_n/avsc12013-toc-0001.gif?v=1&amp;s=0ec53f8a3f0c6f4b1848c4193405638d5cd63ec4"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The study investigates the reaction of species and assemblages to disturbance, P-fertilization and irrigation in a Mediterranean grassland. Disturbance favours annuals, especially those with persistent seed banks. Repeated disturbance favours prostrate species while cessation of disturbance leads to the rapid recovery of biomass production. P-fertilization favours legumes in the short term while irrigation has no obvious effect on species composition.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Aims
(1) To investigate the temporal response of semi-arid Mediterranean grasslands to multiple disturbances as well as P fertilization and irrigation; and (2) to determine the reaction of single species or groups of species as well as the extent of recovery of the grassland community following cessation of the above interventions.


Location
North Greece.


Methods
In a fenced area, six treatments (burning, irrigation, digging, cutting, P fertilization and control) were applied, for three growing seasons, in a completely randomized block design with four blocks. Biomass was sampled in five (0.5 × 0.5 m) quadrats per plot at the end of the growing season and sorted into the following functional groups: annual grasses, perennial grasses, annual legumes and forbs (that included all the other species). Measurements were repeated 1 and 7 yr after cessation of the treatments.


Results
Annual grasses and legumes were positively favoured by cutting, burning and digging, which produced changes in vegetation composition over time. P fertilization had a positive influence on total legume biomass. Effects on individual species were not uniform. Plant composition after cessation of the disturbance treatments was quite different. Total legume biomass remained high 1 yr after the cessation of P fertilization but declined thereafter. Annual grasses and legumes constituted the largest portion of the total biomass in the first year of the experiment. Disturbance (burning, cutting and digging) gradually reduced their biomass in favour of forbs. Seven years after cessation of the treatments, the tall annual, as well as perennial grasses constituted more than 80% of the total biomass. Under conditions of disturbance, short annual species had an advantage over perennials, while cessation of disturbance enables perennial grasses to dominate.


Conclusions
Disturbance promotes the dominance of annuals, especially species with a persistent seed bank. Repeated disturbance encourages an increase of small or prostrate species. Cessation of disturbance leads to the rapid recovery of biomass production. Tall annuals are promoted. P fertilization clearly favours legumes in the short term.

The study investigates the reaction of species and assemblages to disturbance, P-fertilization and irrigation in a Mediterranean grassland. Disturbance favours annuals, especially those with persistent seed banks. Repeated disturbance favours prostrate species while cessation of disturbance leads to the rapid recovery of biomass production. P-fertilization favours legumes in the short term while irrigation has no obvious effect on species composition.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12004" xmlns="http://purl.org/rss/1.0/"><title>Comparison of species and trait-based approaches for describing sagebrush steppe response to range management</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12004</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparison of species and trait-based approaches for describing sagebrush steppe response to range management</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Emily Kachergis, Monique E. Rocca, Maria E. Fernandez-Gimenez</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-01T03:40:20.228373-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12004</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12004</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12004</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12004-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Is valuable information lost when plant trait group composition is used, rather than species composition, to describe plant community response to range management?</p></div></div>
<div class="section" id="avsc12004-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Elkhead Watershed, Colorado, US.</p></div></div>
<div class="section" id="avsc12004-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Current model-building efforts use species composition to define changes in ecosystem state, but plant traits may offer a faster and more broadly applicable alternative. We (1) compare states defined by species composition to those defined by trait-based groups of differing complexity and (2) determine how management and environmental site characteristics relate to species- and trait group-defined states. We sampled 72 plots with different grazing and chemical shrub treatment histories on two soil types. We measured plant species composition in each plot and categorized species into trait groups using three classification schemes, which represented increasing numbers of traits and levels of classification complexity. The classifications employed easily measured traits that affect plant response to range management: life form, life history, resprouting ability, height, vegetative reproduction and N-fixation. Using hierarchical cluster analysis, we identified states with similar species or trait group composition. We explored relationships between each set of potential states and management history and environmental factors using logistic regression.</p></div></div>
<div class="section" id="avsc12004-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Trait-based group composition and species composition identified many of the same potential states and responses to grazing and chemical shrub treatment. Relationships between species and trait group composition and management and environmental characteristics differed on the two soil types. Species composition was sensitive to more different management practices, on average, than trait group composition. Trait group composition revealed some relationships to management and environmental drivers that were not detected using species composition.</p></div></div>
<div class="section" id="avsc12004-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>This study confirms that species composition is a more sensitive indicator of sagebrush steppe response to range management, and some information is lost with a trait-based approach. However, traits also add to depth of understanding by revealing additional community patterns related to different drivers. Using the most complex trait grouping scheme that is feasible in a particular study, and also looking for patterns based on simpler trait groups, will provide the most complete understanding of sagebrush steppe response to range management.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12004/asset/image_m/avsc12004-toc-0001-m.png?v=1&amp;s=6cfa4a0889454ecc8b4568b76890d8d19e0f019b" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12004/asset/image_n/avsc12004-toc-0001.gif?v=1&amp;s=4e0b62d9b346e10a4c2efc8bc486455c4c1de7ed"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Is valuable information lost when trait group composition is used instead of species composition for describing vegetation dynamics? In the sagebrush steppe, we found that some information is lost: species composition is a more sensitive indicator of vegetation response to range management. However, traits contributed to understanding by revealing additional patterns related to different drivers. The two approaches are complementary. 
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Is valuable information lost when plant trait group composition is used, rather than species composition, to describe plant community response to range management?


Location
Elkhead Watershed, Colorado, US.


Methods
Current model-building efforts use species composition to define changes in ecosystem state, but plant traits may offer a faster and more broadly applicable alternative. We (1) compare states defined by species composition to those defined by trait-based groups of differing complexity and (2) determine how management and environmental site characteristics relate to species- and trait group-defined states. We sampled 72 plots with different grazing and chemical shrub treatment histories on two soil types. We measured plant species composition in each plot and categorized species into trait groups using three classification schemes, which represented increasing numbers of traits and levels of classification complexity. The classifications employed easily measured traits that affect plant response to range management: life form, life history, resprouting ability, height, vegetative reproduction and N-fixation. Using hierarchical cluster analysis, we identified states with similar species or trait group composition. We explored relationships between each set of potential states and management history and environmental factors using logistic regression.


Results
Trait-based group composition and species composition identified many of the same potential states and responses to grazing and chemical shrub treatment. Relationships between species and trait group composition and management and environmental characteristics differed on the two soil types. Species composition was sensitive to more different management practices, on average, than trait group composition. Trait group composition revealed some relationships to management and environmental drivers that were not detected using species composition.


Conclusion
This study confirms that species composition is a more sensitive indicator of sagebrush steppe response to range management, and some information is lost with a trait-based approach. However, traits also add to depth of understanding by revealing additional community patterns related to different drivers. Using the most complex trait grouping scheme that is feasible in a particular study, and also looking for patterns based on simpler trait groups, will provide the most complete understanding of sagebrush steppe response to range management.

Is valuable information lost when trait group composition is used instead of species composition for describing vegetation dynamics? In the sagebrush steppe, we found that some information is lost: species composition is a more sensitive indicator of vegetation response to range management. However, traits contributed to understanding by revealing additional patterns related to different drivers. The two approaches are complementary. 







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12011" xmlns="http://purl.org/rss/1.0/"><title>Impacts of Tamarix-mediated soil changes on restoration plant growth</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12011</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Impacts of Tamarix-mediated soil changes on restoration plant growth</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Erik A. Lehnhoff, Fabian D. Menalled</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-27T18:46:36.401328-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12011</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12011</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12011</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12011-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Do soils impacted by <em>Tamarix</em> spp. affect the growth of plants used for restoration through altered soil chemistry and/or plant-soil feedbacks?</p></div></div>
<div class="section" id="avsc12011-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>The Bighorn River, the Yellowstone River and the Fort Peck Reservoir, Montana, western USA.</p></div></div>
<div class="section" id="avsc12011-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Soil was collected from paired subsites where <em>Tamarix</em> was either present or absent along three water bodies. To evaluate chemical and biological soil effects on plant growth, eight plant species (<em>Achnatherum hymenoides</em>,<em> Astragalus cicer</em>,<em> Dalea candida</em>,<em> Elymus lanceolatus</em>,<em> Leymus cinereus</em>,<em> Pascopyrum smithii</em>,<em> Ratibida columnifera</em> and <em>Trifolium pratense</em>) commonly used in restoration projects at <em>Tamarix</em>-invaded sites were grown in the collected soil. Plant-soil feedbacks were evaluated by growing two species (<em>D. candida</em> and <em>P. smithii</em>) in greenhouse soils inoculated with small amounts of the field soils. Germination, emergence and growth characteristics were compared between <em>Tamarix</em>-invaded and un-invaded subsites and across water bodies.</p></div></div>
<div class="section" id="avsc12011-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Seedling emergence and plant relative growth rate, total biomass production and allocation of resources to roots and shoots were not negatively affected in field soils or in greenhouse soil inoculated with soil from areas where <em>Tamarix</em> was present. In fact, overall, plants emerged earlier and produced more biomass in soils affected by <em>Tamarix</em> than in soils from where <em>Tamarix</em> was not present. These results indicate that for sites in the northern range of <em>Tamarix</em>, restoration would not be inhibited by <em>Tamarix</em>-induced soil changes.</p></div></div>
<div class="section" id="avsc12011-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p><em>Tamarix</em> is a relatively new invader in the northern USA, and little is known about its impacts in this area or the potential implications for restoration. However, our results indicate that neither altered soil chemistry nor plant-soil feedbacks negatively impact native plant growth, and restoration efforts would not be hindered by <em>Tamarix</em>-induced changes to soil chemistry or microbiota.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12011/asset/image_m/avsc12011-toc-0001-m.png?v=1&amp;s=ff82e3d7f75e3d0bb47791079f6467c78a0477f3" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12011/asset/image_n/avsc12011-toc-0001.gif?v=1&amp;s=d2136dbaac3d5c166b29e65c165545945bc00504"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Some non-native plants can induce soil chemistry changes or biologically-mediated plant-soil feedbacks (PSF) that negatively affect other species. The impact of the non-native <em>Tamarix</em> spp. on the growth of other plant species was evaluated for soils from three water bodies in Montana (USA). Altered soil chemistry increased plant growth, but biological PSF did not impact the growth of other species.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Do soils impacted by Tamarix spp. affect the growth of plants used for restoration through altered soil chemistry and/or plant-soil feedbacks?


Location
The Bighorn River, the Yellowstone River and the Fort Peck Reservoir, Montana, western USA.


Methods
Soil was collected from paired subsites where Tamarix was either present or absent along three water bodies. To evaluate chemical and biological soil effects on plant growth, eight plant species (Achnatherum hymenoides, Astragalus cicer, Dalea candida, Elymus lanceolatus, Leymus cinereus, Pascopyrum smithii, Ratibida columnifera and Trifolium pratense) commonly used in restoration projects at Tamarix-invaded sites were grown in the collected soil. Plant-soil feedbacks were evaluated by growing two species (D. candida and P. smithii) in greenhouse soils inoculated with small amounts of the field soils. Germination, emergence and growth characteristics were compared between Tamarix-invaded and un-invaded subsites and across water bodies.


Results
Seedling emergence and plant relative growth rate, total biomass production and allocation of resources to roots and shoots were not negatively affected in field soils or in greenhouse soil inoculated with soil from areas where Tamarix was present. In fact, overall, plants emerged earlier and produced more biomass in soils affected by Tamarix than in soils from where Tamarix was not present. These results indicate that for sites in the northern range of Tamarix, restoration would not be inhibited by Tamarix-induced soil changes.


Conclusions
Tamarix is a relatively new invader in the northern USA, and little is known about its impacts in this area or the potential implications for restoration. However, our results indicate that neither altered soil chemistry nor plant-soil feedbacks negatively impact native plant growth, and restoration efforts would not be hindered by Tamarix-induced changes to soil chemistry or microbiota.

Some non-native plants can induce soil chemistry changes or biologically-mediated plant-soil feedbacks (PSF) that negatively affect other species. The impact of the non-native Tamarix spp. on the growth of other plant species was evaluated for soils from three water bodies in Montana (USA). Altered soil chemistry increased plant growth, but biological PSF did not impact the growth of other species.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12007" xmlns="http://purl.org/rss/1.0/"><title>Salt application as an effective measure to control ruderal invaders threatening endangered halophytic plant species</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12007</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Salt application as an effective measure to control ruderal invaders threatening endangered halophytic plant species</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zeeba Khan, Matthias Albrecht, Anna Traveset</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-20T06:43:21.211472-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12007</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12007</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12007</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12007-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How does salinity affect germination, seedling performance and survival of the critically endangered <em>Limonium barceloi,</em> compared to ruderal species invading its salt marsh habitat? Is salt application an effective management tool for controlling invaders and favouring endangered halophytes?</p></div></div>
<div class="section" id="avsc12007-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Ses Fontanelles, Mallorca, Balearic Islands, Spain.</p></div></div>
<div class="section" id="avsc12007-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>The germination of seeds of <em>L. barceloi</em> and nine ruderal species was tested in five salinity levels (0–37 g·L<sup>−1</sup>), and also in freshwater after a pre-treatment with seawater. The ruderal study species were: <em>Asphodelus fistulosus, Avena barbata</em>,<em> Geranium molle</em>,<em> Hypochoeris achyrophorus</em>,<em> Oryzopsis miliacea</em>,<em> Plantago coronopus, Reichardia picroides, Sonchus asper</em> and <em>Sonchus tenerrimus</em>. Two salt concentration levels (18 and 37 g·L<sup>−1</sup>) were applied twice monthly, weekly or twice weekly to examine the effect of salt irrigation schemes on the performance and seedling survival of <em>L. barceloi</em> compared to two of the principal species invading these salt marshes, <em>S. tenerrimus</em> and <em>A. fistulosus</em>.</p></div></div>
<div class="section" id="avsc12007-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Germination of <em>L. barceloi</em> and most ruderal species was highest at low salinity (0–8 g·L<sup>−1</sup>). Seeds of <em>L. barceloi, A. fistulosus</em> and <em>S. tenerrimus</em> were also able to germinate at the highest salinity level, in contrast to the other species. Germination in freshwater after seawater pre-treatment was highest in <em>L. barceloi</em> (72 ± 6%). Seedling performance and survival of <em>A. fistulosus</em> and <em>S. tenerrimus</em> decreased with frequency and concentration of the salt treatment. An application of 37 g·L<sup>−1</sup> salt twice a week reduced seedling survival of <em>A. fistulosus</em> and <em>S. tenerrimus</em> by 83.3 and 91.6%, respectively. In contrast, 100% of the <em>L. barceloi</em> seedlings survived and showed similar performance among treatments.</p></div></div>
<div class="section" id="avsc12007-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p><em>Limonium barceloi</em> had higher seedling growth and survival than ruderal invaders when salinity levels were high (37 g·L<sup>−1</sup>). Nevertheless, at lower salinity, ruderal species may germinate and grow better and thus salinity level changes may represent a threat to the survival of this critically endangered species. Although further field testing is required, our experiments suggest that salt application could be an effective measure to protect <em>L. barceloi</em> and other endangered halophytic plant species from less salt-tolerant invaders.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12007/asset/image_m/avsc12007-toc-0001-m.png?v=1&amp;s=2bd7a300b75630629d80e20395dd84761025553e" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12007/asset/image_n/avsc12007-toc-0001.gif?v=1&amp;s=6e517eea15e3c75cf707ce339ad751fa3b306b88"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Salt application could be an effective measure to protect endangered halophytic plant species from less salt tolerant invaders. We experimentally tested this for the critically endangered <em>Limonium barceloi</em> and ruderals invading its salt marsh habitat. Seedling performance and survival of the ruderals – in contrast to <em>R. barceloi</em> – strongly decreased with frequency and concentration of the salt treatment.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How does salinity affect germination, seedling performance and survival of the critically endangered Limonium barceloi, compared to ruderal species invading its salt marsh habitat? Is salt application an effective management tool for controlling invaders and favouring endangered halophytes?


Location
Ses Fontanelles, Mallorca, Balearic Islands, Spain.


Methods
The germination of seeds of L. barceloi and nine ruderal species was tested in five salinity levels (0–37 g·L−1), and also in freshwater after a pre-treatment with seawater. The ruderal study species were: Asphodelus fistulosus, Avena barbata, Geranium molle, Hypochoeris achyrophorus, Oryzopsis miliacea, Plantago coronopus, Reichardia picroides, Sonchus asper and Sonchus tenerrimus. Two salt concentration levels (18 and 37 g·L−1) were applied twice monthly, weekly or twice weekly to examine the effect of salt irrigation schemes on the performance and seedling survival of L. barceloi compared to two of the principal species invading these salt marshes, S. tenerrimus and A. fistulosus.


Results
Germination of L. barceloi and most ruderal species was highest at low salinity (0–8 g·L−1). Seeds of L. barceloi, A. fistulosus and S. tenerrimus were also able to germinate at the highest salinity level, in contrast to the other species. Germination in freshwater after seawater pre-treatment was highest in L. barceloi (72 ± 6%). Seedling performance and survival of A. fistulosus and S. tenerrimus decreased with frequency and concentration of the salt treatment. An application of 37 g·L−1 salt twice a week reduced seedling survival of A. fistulosus and S. tenerrimus by 83.3 and 91.6%, respectively. In contrast, 100% of the L. barceloi seedlings survived and showed similar performance among treatments.


Conclusions
Limonium barceloi had higher seedling growth and survival than ruderal invaders when salinity levels were high (37 g·L−1). Nevertheless, at lower salinity, ruderal species may germinate and grow better and thus salinity level changes may represent a threat to the survival of this critically endangered species. Although further field testing is required, our experiments suggest that salt application could be an effective measure to protect L. barceloi and other endangered halophytic plant species from less salt-tolerant invaders.

Salt application could be an effective measure to protect endangered halophytic plant species from less salt tolerant invaders. We experimentally tested this for the critically endangered Limonium barceloi and ruderals invading its salt marsh habitat. Seedling performance and survival of the ruderals – in contrast to R. barceloi – strongly decreased with frequency and concentration of the salt treatment.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12006" xmlns="http://purl.org/rss/1.0/"><title>Differential succession towards woodland along a nutrient gradient</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12006</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Differential succession towards woodland along a nutrient gradient</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Franz Rebele</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-12T06:25:19.985943-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12006</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12006</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12006</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12006-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How do different substrate types and soil nutrient levels influence species composition and successional sequences, as represented by different life-history traits? Is the rate of succession increasing or decreasing along a gradient from low to high fertility?</p></div></div>
<div class="section" id="avsc12006-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Ecological field station Dahlem, Berlin, Germany.</p></div></div>
<div class="section" id="avsc12006-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>An 18-yr permanent plot study of succession on soils of differing fertility. The original substrates were a nutrient-poor sandy soil from a sandpit, ruderal subsoil of moderate fertility and nutrient-rich topsoil.</p></div></div>
<div class="section" id="avsc12006-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>In plots with sand, monocarpic perennials were dominant at the beginning, which were then replaced by perennial grasses, those being then replaced by woody perennials. On ruderal soil, monocarpic perennials were co-dominant with perennial herbs at first, then were replaced by perennial herbs, which were then also replaced by woody plants. Dominance of woody species was attained after about 10 yr, both on sand and on ruderal soil. In plots with topsoil, there was a short phase at the start where monocarpic perennials were co-dominant with perennial herbs, followed by a relatively long period of perennial herb dominance. There were about twice as many woody species growing on the substrates of low and intermediate fertility compared to the nutrient-rich soil. If we compare the time necessary for woody species to reach 10% and 50% cover, woody colonization was much slower on the resource-rich site. DCA ordination revealed a clear separation of samples along the nutrient gradient. It also showed slower community change with increasing soil fertility.</p></div></div>
<div class="section" id="avsc12006-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>This study demonstrates that woodlands can be created on bare ground in a temperate climate through natural colonization in a relatively short time, if substrates are not too nutrient-rich. The assumption that the rate of succession increases with increasing productivity could not be confirmed. Succession towards woodland can be rapid on soils of low and intermediate fertility. In contrast, a nutrient-rich substrate favours perennial herbaceous vegetation, which inhibits woody colonization and arrests succession.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12006/asset/image_m/avsc12006-toc-0001-m.png?v=1&amp;s=ac1b6de5a1319400912410e9621a674044135030" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12006/asset/image_n/avsc12006-toc-0001.gif?v=1&amp;s=233e9c59fb08c4808ad798bff2ad024f3bd378d0"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Woodlands can be created on bare ground in temperate climate by natural colonization in relatively short time. The rate of succession does not increase with increasing productivity. Succession towards woodland can be rapid on soils of low and intermediate fertility. On the contrary, a nutrient-rich substrate favours perennial herbaceous vegetation which inhibits woody colonization and arrest succession.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How do different substrate types and soil nutrient levels influence species composition and successional sequences, as represented by different life-history traits? Is the rate of succession increasing or decreasing along a gradient from low to high fertility?


Location
Ecological field station Dahlem, Berlin, Germany.


Methods
An 18-yr permanent plot study of succession on soils of differing fertility. The original substrates were a nutrient-poor sandy soil from a sandpit, ruderal subsoil of moderate fertility and nutrient-rich topsoil.


Results
In plots with sand, monocarpic perennials were dominant at the beginning, which were then replaced by perennial grasses, those being then replaced by woody perennials. On ruderal soil, monocarpic perennials were co-dominant with perennial herbs at first, then were replaced by perennial herbs, which were then also replaced by woody plants. Dominance of woody species was attained after about 10 yr, both on sand and on ruderal soil. In plots with topsoil, there was a short phase at the start where monocarpic perennials were co-dominant with perennial herbs, followed by a relatively long period of perennial herb dominance. There were about twice as many woody species growing on the substrates of low and intermediate fertility compared to the nutrient-rich soil. If we compare the time necessary for woody species to reach 10% and 50% cover, woody colonization was much slower on the resource-rich site. DCA ordination revealed a clear separation of samples along the nutrient gradient. It also showed slower community change with increasing soil fertility.


Conclusions
This study demonstrates that woodlands can be created on bare ground in a temperate climate through natural colonization in a relatively short time, if substrates are not too nutrient-rich. The assumption that the rate of succession increases with increasing productivity could not be confirmed. Succession towards woodland can be rapid on soils of low and intermediate fertility. In contrast, a nutrient-rich substrate favours perennial herbaceous vegetation, which inhibits woody colonization and arrests succession.

Woodlands can be created on bare ground in temperate climate by natural colonization in relatively short time. The rate of succession does not increase with increasing productivity. Succession towards woodland can be rapid on soils of low and intermediate fertility. On the contrary, a nutrient-rich substrate favours perennial herbaceous vegetation which inhibits woody colonization and arrest succession.








</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12003" xmlns="http://purl.org/rss/1.0/"><title>Drove roads as local biodiversity reservoirs: effects on landscape pattern and plant communities in a Mediterranean region</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12003</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Drove roads as local biodiversity reservoirs: effects on landscape pattern and plant communities in a Mediterranean region</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Francisco M. Azcárate, Irene Robleño, Javier Seoane, Pablo Manzano, Begoña Peco</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-07T04:15:21.245188-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12003</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12003</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12003</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12003-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>What are the effects of traditional drove roads on landscape pattern and plant communities?</p></div></div>
<div class="section" id="avsc12003-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Madrid Autonomous Region, Central Spain.</p></div></div>
<div class="section" id="avsc12003-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We selected four study localities in different landscape units. Within each locality, we selected eight sites and within each site, we established three 1-ha plots, each corresponding to one of three situations: drove road, adjacent matrix or distant matrix. The landscape pattern of each plot was characterized by the cover of the different patch types, the patch type richness ha<sup>−1</sup> and the patch type evenness ha<sup>−1</sup>. At one site per locality, we also recorded vegetation by randomly distributing twenty 20 cm × 20 cm quadrats per plot. We characterized each quadrat by its species richness, plant species composition and plant functional composition. We also analysed species richness by constructing rarefaction curves for each plot.</p></div></div>
<div class="section" id="avsc12003-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>In the localities situated in croplands, sub-mediterranean forests and coniferous forests, drove roads were found to be an important source of spatial heterogeneity and a reservoir for a large number of plant species. In contrast, drove roads did not differ from the matrix habitats in rangelands, suggesting that the processes shaping drove road vegetation are similar to the general processes that shape grazed systems. Drove roads did not imply a significant increase in functional diversity. Our results were heavily scale-dependent: while drove roads provided heterogeneity at the local scale, they showed a remarkable similarity at the large scale.</p></div></div>
<div class="section" id="avsc12003-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Drove roads act as authentic local biodiversity reservoirs, especially in environments with low grazing levels. At the same time, drove roads imply structural and functional continuity on a large scale, increasing potential connectivity at the regional level. We recommend the preservation of drove roads in a functional state, because of their benefits to plant biodiversity conservation, and claim that these benefits should be considered when designing livestock policies with different intensification scenarios.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12003/asset/image_m/avsc12003-toc-0001-m.png?v=1&amp;s=722f85ed7b3a6b3dad709986ba2087c7dc3a2ba9" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12003/asset/image_n/avsc12003-toc-0001.gif?v=1&amp;s=cd35992f7cf08b4ca308f7789ce26ac65ad15b89"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The corridors used by pastoralists to move their animals to seasonal pastures are known to be key for plant dispersal, but their role hosting biodiversity has not been properly quantified. This case study from Central Spain shows that they increase local richness by increasing habitat heterogeneity. Given the extent of pastoralism, the implications for biodiversity conservation have a global reach.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
What are the effects of traditional drove roads on landscape pattern and plant communities?


Location
Madrid Autonomous Region, Central Spain.


Methods
We selected four study localities in different landscape units. Within each locality, we selected eight sites and within each site, we established three 1-ha plots, each corresponding to one of three situations: drove road, adjacent matrix or distant matrix. The landscape pattern of each plot was characterized by the cover of the different patch types, the patch type richness ha−1 and the patch type evenness ha−1. At one site per locality, we also recorded vegetation by randomly distributing twenty 20 cm × 20 cm quadrats per plot. We characterized each quadrat by its species richness, plant species composition and plant functional composition. We also analysed species richness by constructing rarefaction curves for each plot.


Results
In the localities situated in croplands, sub-mediterranean forests and coniferous forests, drove roads were found to be an important source of spatial heterogeneity and a reservoir for a large number of plant species. In contrast, drove roads did not differ from the matrix habitats in rangelands, suggesting that the processes shaping drove road vegetation are similar to the general processes that shape grazed systems. Drove roads did not imply a significant increase in functional diversity. Our results were heavily scale-dependent: while drove roads provided heterogeneity at the local scale, they showed a remarkable similarity at the large scale.


Conclusions
Drove roads act as authentic local biodiversity reservoirs, especially in environments with low grazing levels. At the same time, drove roads imply structural and functional continuity on a large scale, increasing potential connectivity at the regional level. We recommend the preservation of drove roads in a functional state, because of their benefits to plant biodiversity conservation, and claim that these benefits should be considered when designing livestock policies with different intensification scenarios.

The corridors used by pastoralists to move their animals to seasonal pastures are known to be key for plant dispersal, but their role hosting biodiversity has not been properly quantified. This case study from Central Spain shows that they increase local richness by increasing habitat heterogeneity. Given the extent of pastoralism, the implications for biodiversity conservation have a global reach.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12005" xmlns="http://purl.org/rss/1.0/"><title>Quantitative vs qualitative vegetation sampling methods: a lesson from a grazing experiment in a Mediterranean grassland</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12005</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Quantitative vs qualitative vegetation sampling methods: a lesson from a grazing experiment in a Mediterranean grassland</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carly Golodets, Jaime Kigel, Yuval Sapir, Marcelo Sternberg</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-10-24T06:23:26.49897-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12005</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12005</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12005</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12005-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>How well does a time-saving, qualitative sampling method compare with an intensive, quantitative sampling method in identifying the effects of reduction and cessation of cattle grazing on compositional change in a Mediterranean grassland?</p></div></div>
<div class="section" id="avsc12005-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Upper Galilee, northern Israel.</p></div></div>
<div class="section" id="avsc12005-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Experimental treatments involved two levels of grazing intensity and protection from grazing for different time periods. Sampling methods included a quantitative method, involving harvesting of vegetative biomass from small (25 × 25 cm) quadrats within 10 × 10 m exclosures, and a qualitative method, involving recording presence only of plant species within the same exclosures.</p></div></div>
<div class="section" id="avsc12005-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Both sampling methods revealed differences between protected vegetation and grazed vegetation; however they were not comparable in the way they described differences in species composition between grazed and ungrazed vegetation, and neither method could discriminate between the two levels of grazing intensity. The discrepancy between the two methods in the number and identity of species recorded ranged from 37% to 51% per plot for species recorded by both methods.</p></div></div>
<div class="section" id="avsc12005-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Qualitative sampling highlighted species that are indicative of protection from grazing; however it did not satisfactorily describe alteration in community composition, since the studied grassland is characterized by changing dominance of common species among treatments, instead of major species turnover. Suitable methods of data collection and monitoring will depend primarily on manpower and the specific characteristics of the studied community.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12005/asset/image_m/avsc12005-toc-0001-m.png?v=1&amp;s=c31af9c21339c33e2aefc3d3201aa1ef710a2033" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12005/asset/image_n/avsc12005-toc-0001.gif?v=1&amp;s=a70553e5bba24127e1b25241fb5aa3b9a3dbd8bc"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We compared how qualitative and quantitative sampling methods identified effects of cattle grazing on species composition in a Mediterranean grassland. Both methods revealed differences between grazed and ungrazed vegetation, but not between grazing intensities. Qualitative sampling was faster, but did not satisfactorily describe changes in species composition. The research highlights the importance of community characteristics for determining suitable sampling methods.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
How well does a time-saving, qualitative sampling method compare with an intensive, quantitative sampling method in identifying the effects of reduction and cessation of cattle grazing on compositional change in a Mediterranean grassland?


Location
Upper Galilee, northern Israel.


Methods
Experimental treatments involved two levels of grazing intensity and protection from grazing for different time periods. Sampling methods included a quantitative method, involving harvesting of vegetative biomass from small (25 × 25 cm) quadrats within 10 × 10 m exclosures, and a qualitative method, involving recording presence only of plant species within the same exclosures.


Results
Both sampling methods revealed differences between protected vegetation and grazed vegetation; however they were not comparable in the way they described differences in species composition between grazed and ungrazed vegetation, and neither method could discriminate between the two levels of grazing intensity. The discrepancy between the two methods in the number and identity of species recorded ranged from 37% to 51% per plot for species recorded by both methods.


Conclusions
Qualitative sampling highlighted species that are indicative of protection from grazing; however it did not satisfactorily describe alteration in community composition, since the studied grassland is characterized by changing dominance of common species among treatments, instead of major species turnover. Suitable methods of data collection and monitoring will depend primarily on manpower and the specific characteristics of the studied community.

We compared how qualitative and quantitative sampling methods identified effects of cattle grazing on species composition in a Mediterranean grassland. Both methods revealed differences between grazed and ungrazed vegetation, but not between grazing intensities. Qualitative sampling was faster, but did not satisfactorily describe changes in species composition. The research highlights the importance of community characteristics for determining suitable sampling methods.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12014" xmlns="http://purl.org/rss/1.0/"><title>Can exotic pine trees assist in restoration?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12014</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Can exotic pine trees assist in restoration?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David A. Norton, Adam Forbes</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T03:29:13.726586-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12014</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12014</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12014</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Commentary</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">169</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">170</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Invasive exotic woody species, including conifers escaped from plantations, are usually regarded as serious threats to native biodiversity. Becerra &amp; Montenegro (<em>Applied Vegetation Science,</em> 16, 2013, 2) present an interesting example of invasive <em>Pinus radiata</em> facilitating native woody regeneration in semi-arid central Chile. However, the positive value of invasive conifers for restoration and conservation will not necessarily apply in all situations.</p></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12014/asset/image_m/avsc12014-toc-0001-m.png?v=1&amp;s=65cb37caed0360dc629708968ae8890dfa902d72" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12014/asset/image_n/avsc12014-toc-0001.gif?v=1&amp;s=5f33693d1dd7571413489e9d0fdaa87a20ee03aa"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Invasive exotic woody species, including conifers escaped from plantations, are usually regarded as serious threats to native biodiversity. Becerra &amp; Montenegro (<em>Applied Vegetation Science,</em> 16, 2013, 2) present an interesting example of invasive <em>Pinus radiata</em> facilitating native woody regeneration in semi-arid central Chile. However, the positive value of invasive conifers for restoration and conservation will not necessarily apply in all situations.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>

Invasive exotic woody species, including conifers escaped from plantations, are usually regarded as serious threats to native biodiversity. Becerra &amp; Montenegro (Applied Vegetation Science, 16, 2013, 2) present an interesting example of invasive Pinus radiata facilitating native woody regeneration in semi-arid central Chile. However, the positive value of invasive conifers for restoration and conservation will not necessarily apply in all situations.
Invasive exotic woody species, including conifers escaped from plantations, are usually regarded as serious threats to native biodiversity. Becerra &amp; Montenegro (Applied Vegetation Science, 16, 2013, 2) present an interesting example of invasive Pinus radiata facilitating native woody regeneration in semi-arid central Chile. However, the positive value of invasive conifers for restoration and conservation will not necessarily apply in all situations.





</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12022" xmlns="http://purl.org/rss/1.0/"><title>Local trait organization established</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12022</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Local trait organization established</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ingolf Kühn</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-04T03:29:13.726586-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12022</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12022</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12022</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Commentary</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">171</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">172</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Traditionally, ecological theory on community assembly and <em>Applied Vegetation Science</em> are considered distinct. Fischer et al. (this issue of <em>Applied Vegetation Science</em>), however, show neatly how differences in trait composition between resident and colonizing species could be established. By using an environmental context-specific approach, the analysis bridges the gap between application and more theoretical understanding of vegetation ecology.</p></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12022/asset/image_m/avsc12022-toc-0001-m.png?v=1&amp;s=753f349e865bbe01d64e0ea0887a6a19a101aa7f" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12022/asset/image_n/avsc12022-toc-0001.gif?v=1&amp;s=fde16ff455f1b822234446ee32147b832a6a1482"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Traditionally, ecological theory on community assembly and applied vegetation science are considered distinct. Fischer et al. (this issue of <em>Applied Vegetation Science</em>), however, show neatly how differences in trait composition between resident and colonizing species could be established. By using an environmental context-specific approach, the analysis bridges the gap between application and more theoretical understanding of vegetation ecology.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>

Traditionally, ecological theory on community assembly and Applied Vegetation Science are considered distinct. Fischer et al. (this issue of Applied Vegetation Science), however, show neatly how differences in trait composition between resident and colonizing species could be established. By using an environmental context-specific approach, the analysis bridges the gap between application and more theoretical understanding of vegetation ecology.
Traditionally, ecological theory on community assembly and applied vegetation science are considered distinct. Fischer et al. (this issue of Applied Vegetation Science), however, show neatly how differences in trait composition between resident and colonizing species could be established. By using an environmental context-specific approach, the analysis bridges the gap between application and more theoretical understanding of vegetation ecology.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01221.x" xmlns="http://purl.org/rss/1.0/"><title>The widely invasive tree Pinus radiata facilitates regeneration of native woody species in a semi-arid ecosystem</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01221.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The widely invasive tree Pinus radiata facilitates regeneration of native woody species in a semi-arid ecosystem</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pablo I. Becerra, Gloria Montenegro</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-23T03:02:13.314407-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01221.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01221.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01221.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">173</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">183</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1221-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>What is the effect of invading individuals of the widely invasive species <em>Pinus radiata </em>D. Don on regeneration of native woody species in a semi-arid ecosystem?</p></div></div>
<div class="section" id="avsc1221-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>A semi-arid ecosystem in central Chile.</p></div></div>
<div class="section" id="avsc1221-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We sampled natural regeneration of native woody species in 40 plots in each of three canopy types: (1) under young adult invading trees of <em>P</em>. <em>radiata</em> located in formerly open (disturbed) sites; (2) in patches of native trees; and (3) in open (disturbed) sites, in two localities where this exotic tree is invading. Additionally, we carried out a field experiment in one of these localities; in eight of each of these canopy types we sowed seeds of ten widely distributed woody native species and monitored their recruitment. We also assessed different biotic and abiotic variables in these canopy types.</p></div></div>
<div class="section" id="avsc1221-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>We found that soil water content, depth and cover of leaf litter were higher and photosythetically active radiation was lower under <em>P. radiata</em> trees and native patches than in open sites. In the natural regeneration study, species richness of seedlings was higher in native patches and under <em>P. radiata</em> trees than in open sites, and total abundance of seedlings (including all species) was higher only in native patches than in open sites. In the field experiment, both species richness and total abundance of seedlings were higher in native patches and under <em>P. radiata</em> trees than in open sites. Moreover, in the field experiment species richness recruiting in native patches was higher than under <em>P. radiata</em> trees.</p></div></div>
<div class="section" id="avsc1221-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>We suggest that native patches as well as <em>P. radiata</em> trees invading open sites facilitate or have the potential to facilitate regeneration of native species, although facilitation produced by native trees was stronger than that produced by <em>P. radiata</em>. Thus, in sites where nurse plants are not available, invasion by this exotic tree may be exploited in restoration processes through sowing or planting native species under the canopy of invading young trees of <em>P. radiata</em>, eliminating <em>P. radiata</em> individuals after native regeneration has established.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01221.x/asset/image_m/avsc1221-toc-0001-m.png?v=1&amp;s=3d6448da001dc9186816a978245b092fadfa8e46" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01221.x/asset/image_n/avsc1221-toc-0001.gif?v=1&amp;s=98d3aeef39e26fa3ea2677e2d7d2211d88d2b049"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In this paper we document that invading individuals of the widely invasive species, <em>Pinus radiata</em>, may facilitates regeneration of native woody species in central Chile, increasing species richness and abundance. We also propose that invasion by this exotic tree may be exploited in restoration processes in semiarid ecosystems by using invading individuals as nurse plants for native species. </p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
What is the effect of invading individuals of the widely invasive species Pinus radiata D. Don on regeneration of native woody species in a semi-arid ecosystem?


Location
A semi-arid ecosystem in central Chile.


Methods
We sampled natural regeneration of native woody species in 40 plots in each of three canopy types: (1) under young adult invading trees of P. radiata located in formerly open (disturbed) sites; (2) in patches of native trees; and (3) in open (disturbed) sites, in two localities where this exotic tree is invading. Additionally, we carried out a field experiment in one of these localities; in eight of each of these canopy types we sowed seeds of ten widely distributed woody native species and monitored their recruitment. We also assessed different biotic and abiotic variables in these canopy types.


Results
We found that soil water content, depth and cover of leaf litter were higher and photosythetically active radiation was lower under P. radiata trees and native patches than in open sites. In the natural regeneration study, species richness of seedlings was higher in native patches and under P. radiata trees than in open sites, and total abundance of seedlings (including all species) was higher only in native patches than in open sites. In the field experiment, both species richness and total abundance of seedlings were higher in native patches and under P. radiata trees than in open sites. Moreover, in the field experiment species richness recruiting in native patches was higher than under P. radiata trees.


Conclusions
We suggest that native patches as well as P. radiata trees invading open sites facilitate or have the potential to facilitate regeneration of native species, although facilitation produced by native trees was stronger than that produced by P. radiata. Thus, in sites where nurse plants are not available, invasion by this exotic tree may be exploited in restoration processes through sowing or planting native species under the canopy of invading young trees of P. radiata, eliminating P. radiata individuals after native regeneration has established.

In this paper we document that invading individuals of the widely invasive species, Pinus radiata, may facilitates regeneration of native woody species in central Chile, increasing species richness and abundance. We also propose that invasion by this exotic tree may be exploited in restoration processes in semiarid ecosystems by using invading individuals as nurse plants for native species. 





</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01227.x" xmlns="http://purl.org/rss/1.0/"><title>Ecological resistance to Acer negundo invasion in a European riparian forest: relative importance of environmental and biotic drivers</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01227.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ecological resistance to Acer negundo invasion in a European riparian forest: relative importance of environmental and biotic drivers</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Patrick Saccone, Jacky Girel, Jean-Philippe Pages, Jean-Jacques Brun, Richard Michalet</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-10T09:23:21.274373-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01227.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01227.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01227.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">184</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">192</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1227-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>The relative importance of environmental vs. biotic resistance of recipient ecological communities remains poorly understood in invasion ecology. <em>Acer negundo</em>, a North American tree, has widely invaded riparian forests throughout Europe at the ecotone between early- (<em>Salix</em> spp. and <em>Populus</em> spp.) and late-successional (<em>Fraxinus</em> spp.) species. However, it is not present in the upper part of the Rhône River, where native <em>Alnus incana</em> occurs at an intermediate position along the successional riparian gradient. Is this absence of the invasive tree due to environmental or biotic resistance of the recipient communities, and in particular due to the presence of <em>Alnus</em>?</p></div></div>
<div class="section" id="avsc1227-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Upper Rhône River, France.</p></div></div>
<div class="section" id="avsc1227-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We undertook a transplant experiment in an <em>Alnus</em>-dominated community along the Upper Rhône River, where we compared <em>Acer negundo</em> survival and growth, with and without biotic interactions (tree and herb layer effects), to those of four native tree species from differing successional positions in the Upper Rhône communities (<em>P. alba</em>,<em> S. alba</em>,<em> F. excelsior</em> and <em>Alnus incana</em>).</p></div></div>
<div class="section" id="avsc1227-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Without biotic interactions <em>Acer negundo</em> performed similarly to native species, suggesting that the Upper Rhône floodplain is not protected from <em>Acer</em> invasion by a simple abiotic barrier. In contrast, this species performed less well than <em>F. excelsior</em> and <em>Alnus incana</em> in environments with intact tree and/or herb layers. <em>Alnus</em> showed the best growth rate in these conditions, indicating biotic resistance of the native plant community.</p></div></div>
<div class="section" id="avsc1227-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>We did not find evidence for an abiotic barrier to <em>Acer negundo</em> invasion of the Upper Rhône River floodplain communities, but our results suggest a biotic resistance. In particular, we demonstrated that (i) additive competitive effects of the tree and herb layer led to <em>Acer negundo</em> suppression and (ii) <em>Alnus incana</em> grew more rapidly than <em>Acer negundo</em> in this intermediate successional niche.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01227.x/asset/image_m/avsc1227-toc-0001-m.png?v=1&amp;s=ae3772daf794101d4357c089b9997cd111a2e21d" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01227.x/asset/image_n/avsc1227-toc-0001.gif?v=1&amp;s=95b90f653a44ecfdedbe4c8f2a4c160e479e8573"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In this study we investigated how plant-plant interactions contributed to the <em>Alnus incana</em> riparian communities of the French Upper Rhone River resistance to <em>Acer negundo</em> invasion. Our results showed that in the presence of tree canopy and herb layer the <em>Acer</em> seedling survival strongly decreased compared to open areas and the <em>Alnus</em> growth rate was twice than those of other species.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
The relative importance of environmental vs. biotic resistance of recipient ecological communities remains poorly understood in invasion ecology. Acer negundo, a North American tree, has widely invaded riparian forests throughout Europe at the ecotone between early- (Salix spp. and Populus spp.) and late-successional (Fraxinus spp.) species. However, it is not present in the upper part of the Rhône River, where native Alnus incana occurs at an intermediate position along the successional riparian gradient. Is this absence of the invasive tree due to environmental or biotic resistance of the recipient communities, and in particular due to the presence of Alnus?


Location
Upper Rhône River, France.


Methods
We undertook a transplant experiment in an Alnus-dominated community along the Upper Rhône River, where we compared Acer negundo survival and growth, with and without biotic interactions (tree and herb layer effects), to those of four native tree species from differing successional positions in the Upper Rhône communities (P. alba, S. alba, F. excelsior and Alnus incana).


Results
Without biotic interactions Acer negundo performed similarly to native species, suggesting that the Upper Rhône floodplain is not protected from Acer invasion by a simple abiotic barrier. In contrast, this species performed less well than F. excelsior and Alnus incana in environments with intact tree and/or herb layers. Alnus showed the best growth rate in these conditions, indicating biotic resistance of the native plant community.


Conclusions
We did not find evidence for an abiotic barrier to Acer negundo invasion of the Upper Rhône River floodplain communities, but our results suggest a biotic resistance. In particular, we demonstrated that (i) additive competitive effects of the tree and herb layer led to Acer negundo suppression and (ii) Alnus incana grew more rapidly than Acer negundo in this intermediate successional niche.

In this study we investigated how plant-plant interactions contributed to the Alnus incana riparian communities of the French Upper Rhone River resistance to Acer negundo invasion. Our results showed that in the presence of tree canopy and herb layer the Acer seedling survival strongly decreased compared to open areas and the Alnus growth rate was twice than those of other species.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01222.x" xmlns="http://purl.org/rss/1.0/"><title>Both complete clearing and thinning of invasive trees lead to short-term recovery of native riparian vegetation in the Western Cape, South Africa</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01222.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Both complete clearing and thinning of invasive trees lead to short-term recovery of native riparian vegetation in the Western Cape, South Africa</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sheunesu Ruwanza, Mirijam Gaertner, Karen J. Esler, David M. Richardson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-15T02:31:49.752864-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01222.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01222.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01222.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">193</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">204</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1222-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>Most rivers in the Western Cape Province of South Africa are heavily invaded by alien trees, often resulting in profound changes in biodiversity and ecosystem functioning. Although large-scale management operations are underway to clear invasive trees and restore ecosystem function, little is known regarding native species recovery after alien clearing. Has <em>Eucalyptus</em> invasion along the Berg River altered the distribution and composition of native vegetation? How does the removal of invasive trees through complete clearing and thinning facilitate the recovery of native vegetation?</p></div></div>
<div class="section" id="avsc1222-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Berg River, Western Cape, South Africa.</p></div></div>
<div class="section" id="avsc1222-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We assessed the recovery of native vegetation after 4 yr of complete clearing of the invasive tree <em>Eucalyptus camaldulensis</em> (100% alien cover removal) and thinning (40–50% alien cover removal) along the Berg River in the Western Cape, South Africa. Native and alien plant cover, species richness and diversity were recorded on completely cleared and thinned sites and compared to natural (non-invaded control sites) and <em>E. camaldulensis</em> invaded sites.</p></div></div>
<div class="section" id="avsc1222-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Species richness and diversity were significantly higher in both completely cleared and thinned sites compared to natural and invaded sites. Increases in species richness and diversity in completely cleared and thinned sites were a result of re-invasion by alien herbaceous and graminoid species, which have the potential to hinder native species recovery. Cover of native trees and shrubs was higher in both completely cleared and thinned sites compared to invaded sites. Species composition (relative cover) in completely cleared and thinned sites was similar to species composition in natural sites.</p></div></div>
<div class="section" id="avsc1222-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Both complete clearing and thinning methods promote indigenous vegetation recovery and a positive trajectory towards recovery of ecosystem structure and composition can be expected in future. To improve management operations, a four-stage thinning process that has the potential to facilitate native species recovery is suggested.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01222.x/asset/image_m/avsc1222-toc-0001-m.png?v=1&amp;s=26c07d7f8fdfa992927ad25df27b4427ef77a2c1" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01222.x/asset/image_n/avsc1222-toc-0001.gif?v=1&amp;s=0b3087be83fce73e98ba643dac0479a010f48754"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In this paper we show that both complete clearing and thinning of invasive eucalypts promote indigenous vegetation recovery in riparian ecosystems. The fact that native species re-established without active restoration intervention suggests that the native ecosystem was still resilient enough for autogenic recovery. To improve management operations we suggest a four-stage thinning process that has the potential to facilitate native species recovery. </p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
Most rivers in the Western Cape Province of South Africa are heavily invaded by alien trees, often resulting in profound changes in biodiversity and ecosystem functioning. Although large-scale management operations are underway to clear invasive trees and restore ecosystem function, little is known regarding native species recovery after alien clearing. Has Eucalyptus invasion along the Berg River altered the distribution and composition of native vegetation? How does the removal of invasive trees through complete clearing and thinning facilitate the recovery of native vegetation?


Location
Berg River, Western Cape, South Africa.


Methods
We assessed the recovery of native vegetation after 4 yr of complete clearing of the invasive tree Eucalyptus camaldulensis (100% alien cover removal) and thinning (40–50% alien cover removal) along the Berg River in the Western Cape, South Africa. Native and alien plant cover, species richness and diversity were recorded on completely cleared and thinned sites and compared to natural (non-invaded control sites) and E. camaldulensis invaded sites.


Results
Species richness and diversity were significantly higher in both completely cleared and thinned sites compared to natural and invaded sites. Increases in species richness and diversity in completely cleared and thinned sites were a result of re-invasion by alien herbaceous and graminoid species, which have the potential to hinder native species recovery. Cover of native trees and shrubs was higher in both completely cleared and thinned sites compared to invaded sites. Species composition (relative cover) in completely cleared and thinned sites was similar to species composition in natural sites.


Conclusions
Both complete clearing and thinning methods promote indigenous vegetation recovery and a positive trajectory towards recovery of ecosystem structure and composition can be expected in future. To improve management operations, a four-stage thinning process that has the potential to facilitate native species recovery is suggested.

In this paper we show that both complete clearing and thinning of invasive eucalypts promote indigenous vegetation recovery in riparian ecosystems. The fact that native species re-established without active restoration intervention suggests that the native ecosystem was still resilient enough for autogenic recovery. To improve management operations we suggest a four-stage thinning process that has the potential to facilitate native species recovery. 




</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01228.x" xmlns="http://purl.org/rss/1.0/"><title>Spatio-temporal dynamics of the invasive plant species Elytrigia atherica on natural salt marshes</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01228.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Spatio-temporal dynamics of the invasive plant species Elytrigia atherica on natural salt marshes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Roos M. Veeneklaas, Kees S. Dijkema, Norbert Hecker, Jan P. Bakker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-04T03:50:41.2098-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01228.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01228.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01228.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">205</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">216</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1228-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>In the past decades, the tall native invasive grass, <em>Elytrigia atherica</em>, has been increasing in frequency and dominance on salt marshes along the Wadden Sea coast. Is this rapid expansion an outcome of natural succession or is it driven by anthropogenic eutrophication resulting from atmospheric deposition?</p></div></div>
<div class="section" id="avsc1228-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Salt marshes on four back-barrier islands, Wadden Sea on the coast of the Netherlands and Germany.</p></div></div>
<div class="section" id="avsc1228-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We used a combination of time series of vegetation maps and chronosequence data of four naturally developed salt marshes to address our questions. These salt marshes have not been grazed by livestock or subject to other management regimes. By comparing development within and between four different salt marshes, we were able to study the spatial and temporal dynamics of the community dominated by <em>E. atherica</em> on natural salt marshes.</p></div></div>
<div class="section" id="avsc1228-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The expansion rate of the <em>E. atherica</em> community was highest on young salt marshes (up to 30 yr old) with vertical accretion rates of 0.35 cm·yr<sup>−1</sup>. The rate of expansion decreased on older marshes and the direction reversed, becoming negative, on the oldest marshes (around 90 yr old), which have no vertical accretion and are under waterlogged conditions.</p></div></div>
<div class="section" id="avsc1228-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The expansion of <em>E. atherica</em> on natural, back-barrier islands along the Wadden Sea coast is more influenced by the age of the salt marsh and patterns in vertical accretion of soil than by uniformly spread atmospheric deposition.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01228.x/asset/image_m/avsc1228-toc-0001-m.png?v=1&amp;s=c5abcd72d487a1bfac9cc3a8d702c4a40fcff4ec" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01228.x/asset/image_n/avsc1228-toc-0001.gif?v=1&amp;s=bd69216b47c76d4b5694ce5a988a71b84e1cffe3"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In the past decades an increase of monotonous stands of <em>E. atherica</em> is observed on salt marshes along the Wadden Sea coast. In this study we address the question whether this rapid expansion is driven by anthropogenic eutrophication or is it an outcome of natural succession. Secondly we reveal that there is a world beyond <em>E. atherica</em>. </p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
In the past decades, the tall native invasive grass, Elytrigia atherica, has been increasing in frequency and dominance on salt marshes along the Wadden Sea coast. Is this rapid expansion an outcome of natural succession or is it driven by anthropogenic eutrophication resulting from atmospheric deposition?


Location
Salt marshes on four back-barrier islands, Wadden Sea on the coast of the Netherlands and Germany.


Methods
We used a combination of time series of vegetation maps and chronosequence data of four naturally developed salt marshes to address our questions. These salt marshes have not been grazed by livestock or subject to other management regimes. By comparing development within and between four different salt marshes, we were able to study the spatial and temporal dynamics of the community dominated by E. atherica on natural salt marshes.


Results
The expansion rate of the E. atherica community was highest on young salt marshes (up to 30 yr old) with vertical accretion rates of 0.35 cm·yr−1. The rate of expansion decreased on older marshes and the direction reversed, becoming negative, on the oldest marshes (around 90 yr old), which have no vertical accretion and are under waterlogged conditions.


Conclusions
The expansion of E. atherica on natural, back-barrier islands along the Wadden Sea coast is more influenced by the age of the salt marsh and patterns in vertical accretion of soil than by uniformly spread atmospheric deposition.

In the past decades an increase of monotonous stands of E. atherica is observed on salt marshes along the Wadden Sea coast. In this study we address the question whether this rapid expansion is driven by anthropogenic eutrophication or is it an outcome of natural succession. Secondly we reveal that there is a world beyond E. atherica. 






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01220.x" xmlns="http://purl.org/rss/1.0/"><title>Quantifying landscape change during the last two centuries in Białowieża Primeval Forest</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01220.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Quantifying landscape change during the last two centuries in Białowieża Primeval Forest</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anna Mikusinska, Bernadetta Zawadzka, Tomasz Samojlik, Bogumiła Jędrzejewska, Grzegorz Mikusiński</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-01T03:15:54.860081-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01220.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01220.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01220.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">217</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">226</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1220-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>What changes in character and extent of land use have occurred during the last 200 yr in the Białowieża Primeval Forest (BPF)? Are the landscape transformations described from the multi-temporal analysis of historical maps coherent with vegetation changes expressed by the previous palynological analyses?</p></div></div>
<div class="section" id="avsc1220-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Białowieża Primeval Forest, Polish–Belarusian border.</p></div></div>
<div class="section" id="avsc1220-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We used five historical maps (from 1793 to 1936) and one digital land-use map (1999–2000) to quantify the landscape changes. Land-use types according to historical maps were digitized and georeferenced. The maps were then used for both comparing the extent of cover types in each time step and analysing the nature of change through transition matrices. The sequence of changes concerning the proportion of land-use types was then compared with classes of pollen, which were assumed to represent corresponding vegetation types.</p></div></div>
<div class="section" id="avsc1220-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Most of the area (&gt;70%) has been continuously covered with forest. In the period between 1793 and 1830, the forest declined, being the main donor to agricultural land and villages. In the 20th century, the trend was reversed. We found a significant correlation between the percentage of the main vegetation types derived from historical maps and the corresponding vegetation types, as indicated by pollen, with a mean time lag of 20 yr.</p></div></div>
<div class="section" id="avsc1220-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>The BPF landscape has been quite stable throughout the last 200 yr, mainly due to the high continuity of forest cover. The results obtained from landscape analysis based on maps are coherent with pollen data collected in the same area.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01220.x/asset/image_m/avsc1220-toc-0001-m.png?v=1&amp;s=70774dbb6d281eee6d255a73192e1075b5519b57" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01220.x/asset/image_n/avsc1220-toc-0001.gif?v=1&amp;s=efd504efc833e93cc33f16b216f88fe4d8b46ff1"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Maps covering the period 1793–1999 were used to quantify the landscape change in the Białowieża Primeval Forest. We found that most of the area (&gt;70%) has continuously been covered by forest, although some parts of it had been converted into agricultural land and villages, especially in the 19th century. In the 20th century, the trend was reversed.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
What changes in character and extent of land use have occurred during the last 200 yr in the Białowieża Primeval Forest (BPF)? Are the landscape transformations described from the multi-temporal analysis of historical maps coherent with vegetation changes expressed by the previous palynological analyses?


Location
Białowieża Primeval Forest, Polish–Belarusian border.


Methods
We used five historical maps (from 1793 to 1936) and one digital land-use map (1999–2000) to quantify the landscape changes. Land-use types according to historical maps were digitized and georeferenced. The maps were then used for both comparing the extent of cover types in each time step and analysing the nature of change through transition matrices. The sequence of changes concerning the proportion of land-use types was then compared with classes of pollen, which were assumed to represent corresponding vegetation types.


Results
Most of the area (&gt;70%) has been continuously covered with forest. In the period between 1793 and 1830, the forest declined, being the main donor to agricultural land and villages. In the 20th century, the trend was reversed. We found a significant correlation between the percentage of the main vegetation types derived from historical maps and the corresponding vegetation types, as indicated by pollen, with a mean time lag of 20 yr.


Conclusion
The BPF landscape has been quite stable throughout the last 200 yr, mainly due to the high continuity of forest cover. The results obtained from landscape analysis based on maps are coherent with pollen data collected in the same area.

Maps covering the period 1793–1999 were used to quantify the landscape change in the Białowieża Primeval Forest. We found that most of the area (&gt;70%) has continuously been covered by forest, although some parts of it had been converted into agricultural land and villages, especially in the 19th century. In the 20th century, the trend was reversed.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01215.x" xmlns="http://purl.org/rss/1.0/"><title>Spatial predictions of land-use transitions and associated threats to biodiversity: the case of forest regrowth in mountain grasslands</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01215.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Spatial predictions of land-use transitions and associated threats to biodiversity: the case of forest regrowth in mountain grasslands</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Loïc Pellissier, Maruska Anzini, Luigi Maiorano, Anne Dubuis, Julien Pottier, Pascal Vittoz, Antoine Guisan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-06-21T09:44:37.611883-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01215.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01215.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01215.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">227</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">236</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1215-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Can we predict where forest regrowth caused by abandonment of agricultural activities is likely to occur? Can we assess how it may conflict with grassland diversity hotspots?</p></div></div>
<div class="section" id="avsc1215-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Western Swiss Alps (400–3210 m a.s.l.).</p></div></div>
<div class="section" id="avsc1215-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We used statistical models to predict the location of land abandonment by farmers that is followed by forest regrowth in semi-natural grasslands of the Western Swiss Alps. Six modelling methods (GAM, GBM, GLM, RF, MDA, MARS) allowing binomial distribution were tested on two successive transitions occurring between three time periods. Models were calibrated using data on land-use change occurring between 1979 and 1992 as response, and environmental, accessibility and socio-economic variables as predictors, and these were validated for their capacity to predict the changes observed from 1992 to 2004. Projected probabilities of land-use change from an ensemble forecast of the six models were combined with a model of plant species richness based on a field inventory, allowing identification of critical grassland areas for the preservation of biodiversity.</p></div></div>
<div class="section" id="avsc1215-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Models calibrated over the first land-use transition period predicted the second transition with reasonable accuracy. Forest regrowth occurs where cultivation costs are high and yield potential is low, i.e. on steeper slopes and at higher elevations. Overlaying species richness with land-use change predictions, we identified priority areas for the management and conservation of biodiversity at intermediate elevations.</p></div></div>
<div class="section" id="avsc1215-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Combining land-use change and biodiversity projections, we propose applied management measures for targeted/identified locations to limit the loss of biodiversity that could otherwise occur through loss of open habitats. The same approach could be applied to other types of land-use changes occurring in other ecosystems.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01215.x/asset/image_m/avsc1215-toc-0001-m.png?v=1&amp;s=18e4b9ad24040170c6a480b08a809b62de9af66a" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01215.x/asset/image_n/avsc1215-toc-0001.gif?v=1&amp;s=6021e3ab056d59ca6b09c25a8c7fc8133d4981e9"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Less pervasive than intensification of human activities, land abandonment followed by forest regrowth occurring in more remote areas like mountain can also represent a serious threat to biodiversity through loss of species-rich grasslands. Here we show that the likely location of land abandonment can be predicted and those models can inform on where to protect threatened surfaces of high biodiversity. </p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Can we predict where forest regrowth caused by abandonment of agricultural activities is likely to occur? Can we assess how it may conflict with grassland diversity hotspots?


Location
Western Swiss Alps (400–3210 m a.s.l.).


Methods
We used statistical models to predict the location of land abandonment by farmers that is followed by forest regrowth in semi-natural grasslands of the Western Swiss Alps. Six modelling methods (GAM, GBM, GLM, RF, MDA, MARS) allowing binomial distribution were tested on two successive transitions occurring between three time periods. Models were calibrated using data on land-use change occurring between 1979 and 1992 as response, and environmental, accessibility and socio-economic variables as predictors, and these were validated for their capacity to predict the changes observed from 1992 to 2004. Projected probabilities of land-use change from an ensemble forecast of the six models were combined with a model of plant species richness based on a field inventory, allowing identification of critical grassland areas for the preservation of biodiversity.


Results
Models calibrated over the first land-use transition period predicted the second transition with reasonable accuracy. Forest regrowth occurs where cultivation costs are high and yield potential is low, i.e. on steeper slopes and at higher elevations. Overlaying species richness with land-use change predictions, we identified priority areas for the management and conservation of biodiversity at intermediate elevations.


Conclusions
Combining land-use change and biodiversity projections, we propose applied management measures for targeted/identified locations to limit the loss of biodiversity that could otherwise occur through loss of open habitats. The same approach could be applied to other types of land-use changes occurring in other ecosystems.

Less pervasive than intensification of human activities, land abandonment followed by forest regrowth occurring in more remote areas like mountain can also represent a serious threat to biodiversity through loss of species-rich grasslands. Here we show that the likely location of land abandonment can be predicted and those models can inform on where to protect threatened surfaces of high biodiversity. 





</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01226.x" xmlns="http://purl.org/rss/1.0/"><title>Temporal changes in forest plant communities at different site types</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01226.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Temporal changes in forest plant communities at different site types</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gorik Verstraeten, Lander Baeten, Tine den Broeck, Pieter Frenne, Andreas Demey, Wesley Tack, Bart Muys, Kris Verheyen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-07T06:26:36.256126-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01226.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01226.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01226.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">237</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">247</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1226-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Aims</h4><div class="para"><p>Given the significance of the herbaceous understorey layer for temperate forest ecosystem biodiversity and functioning, it is important to have a thorough understanding of its dynamics in response to environmental change. However, site-specific factors such as soil type may cause differential temporal herb layer changes within a single study area under comparable external pressure. Surprisingly, relatively few studies have examined herb layer changes on different site types within the same forest complex. The aim of this study is to determine the temporal differences in herb vegetation and to compare these for two differing site types in the same forest complex.</p></div></div>
<div class="section" id="avsc1226-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Ancient broad-leaved woodlands traditionally managed as coppice with standards in South Belgium, an area with secondary deposits and a mild temperate climate.</p></div></div>
<div class="section" id="avsc1226-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>In 2008 we re-inventoried 43 vegetation recordings from 1953 to 1954 in forests on two site types (acid and neutral forests). First, we described differences in soil pH, litter and overstorey characteristics between the sites. Next, multivariate analysis, Ellenberg indicator value and CSR signature were used to determine differences in herb layer diversity and composition between both the two survey times and the two site types. Finally, we analysed temporal differences in individual species abundances and frequencies.</p></div></div>
<div class="section" id="avsc1226-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The two site types clearly differed with respect to soil, litter and overstorey characteristics. Temporal changes between the surveys were mostly highly significant on the neutral sites and mostly not significant on the acid sites. On both site types, the species pool size declined. On the neutral site, the mean plot species richness also declined. Based on the plant-derived characteristics (Ellenberg indicator values) of the plots, light availability decreased and nitrogen availability significantly increased on the neutral sites.</p></div></div>
<div class="section" id="avsc1226-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Input of eutrophying deposits and management changes are seen as key drivers of herb layer changes in the study area over the last half-century. However, our study suggests that site characteristics such as parent material and soil pH should also be considered. Together with the key drivers, incorporating differences in site characteristics may improve our understanding of temporal shifts in herb layer vegetation in response to environmental change.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01226.x/asset/image_m/avsc1226-toc-0001-m.png?v=1&amp;s=7975f0f1784b67cb470b0e9da2574e1236172361" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01226.x/asset/image_n/avsc1226-toc-0001.gif?v=1&amp;s=a23fe4a3ec6740dba47ec2d22c6674132bc67f1c"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In 2008, vegetation recordings from 1953 to 1954 were re-inventoried in a forests on two site types in Belgium. The changes on the acidophilous sites where mostly not significant. On the neutrophilous sites, mean plot species richness declined significantly, and based on the plant-derived characteristics of the plots, light availability decreased and nitrogen availability significantly increased.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Aims
Given the significance of the herbaceous understorey layer for temperate forest ecosystem biodiversity and functioning, it is important to have a thorough understanding of its dynamics in response to environmental change. However, site-specific factors such as soil type may cause differential temporal herb layer changes within a single study area under comparable external pressure. Surprisingly, relatively few studies have examined herb layer changes on different site types within the same forest complex. The aim of this study is to determine the temporal differences in herb vegetation and to compare these for two differing site types in the same forest complex.


Location
Ancient broad-leaved woodlands traditionally managed as coppice with standards in South Belgium, an area with secondary deposits and a mild temperate climate.


Methods
In 2008 we re-inventoried 43 vegetation recordings from 1953 to 1954 in forests on two site types (acid and neutral forests). First, we described differences in soil pH, litter and overstorey characteristics between the sites. Next, multivariate analysis, Ellenberg indicator value and CSR signature were used to determine differences in herb layer diversity and composition between both the two survey times and the two site types. Finally, we analysed temporal differences in individual species abundances and frequencies.


Results
The two site types clearly differed with respect to soil, litter and overstorey characteristics. Temporal changes between the surveys were mostly highly significant on the neutral sites and mostly not significant on the acid sites. On both site types, the species pool size declined. On the neutral site, the mean plot species richness also declined. Based on the plant-derived characteristics (Ellenberg indicator values) of the plots, light availability decreased and nitrogen availability significantly increased on the neutral sites.


Conclusion
Input of eutrophying deposits and management changes are seen as key drivers of herb layer changes in the study area over the last half-century. However, our study suggests that site characteristics such as parent material and soil pH should also be considered. Together with the key drivers, incorporating differences in site characteristics may improve our understanding of temporal shifts in herb layer vegetation in response to environmental change.

In 2008, vegetation recordings from 1953 to 1954 were re-inventoried in a forests on two site types in Belgium. The changes on the acidophilous sites where mostly not significant. On the neutrophilous sites, mean plot species richness declined significantly, and based on the plant-derived characteristics of the plots, light availability decreased and nitrogen availability significantly increased.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01224.x" xmlns="http://purl.org/rss/1.0/"><title>Vegetation responses to long-term alkaline cement dust pollution in Pinus sylvestris-dominated boreal forests – niche breadth along the soil pH gradient</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01224.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Vegetation responses to long-term alkaline cement dust pollution in Pinus sylvestris-dominated boreal forests – niche breadth along the soil pH gradient</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jaanus Paal, Polina Degtjarenko, Ave Suija, Jaan Liira</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-13T09:40:39.480179-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01224.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01224.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01224.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">248</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">259</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1224-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How resilient is boreal forest vegetation growing on acidic podzols to the environmental change caused by alkaline kiln dust pollution? How adaptive is the vegetation, when species pool and time for dispersal do not limit? How constant is the species niche breadth along the soil pH gradient?</p></div></div>
<div class="section" id="avsc1224-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Region of 30 km around the Kunda cement plant, northern Estonia (59°30′ N, 26°32′ E), which has been continuously polluted last 140 years.</p></div></div>
<div class="section" id="avsc1224-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We sampled 20 forest stands on sandy gleyic podzols at various distances from the pollution source, leeward and windward of prevailing winds. Data processing: principal components analysis for gradient generalization, indicator species analysis for grouping species along the pollution gradient and generalized linear model analyses to estimate species reaction to pollution, considering covariates.</p></div></div>
<div class="section" id="avsc1224-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The impact of alkaline dust accumulated over a century persisted despite resolute reductions of pollution. Forest soil conditions changed 10 km leeward and 5 km windward from the source: the litter pH level changed from 3.6 to 4.5 in unpolluted forests to 7.1–7.4 in the heavily polluted forests, and soil Ca content increased ten-fold. Soil alkalization has induced a remarkable succession from typical boreal vegetation toward vegetation of boreo-nemoral or calcareous habitats. We detected a linear increase of species richness from habitats on acidic soils (unpolluted) to newly formed alkaline soils (polluted habitats), reflecting the species pool composition and size, which is known to be large for calcicolous species. The establishment of several endangered calcicolous species shows the lack of dispersal limitation and points on their narrow soil pH niche. The niche breadth of species along the pH gradient varied among species, but only a few species appeared to be pH generalists.</p></div></div>
<div class="section" id="avsc1224-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Species ranking along the pH and/or <span class="fixed-roman">Ca</span> gradients indicates (1) the existence of different ecological guilds in terms of ecological niche use, and (2) the formation of a new community is dictated by the tolerance level of each species. This supports the individualistic community assembly rule suggested by Gleason. We find that such polluted regions with disturbed communities have high scientific value as long-term ecological experiments, but this might lead to conflict between the peculiar biodiversity complex and human well-being.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01224.x/asset/image_m/avsc1224-toc-0001-m.png?v=1&amp;s=693fde6ab8153afced0790dd4fa9dfb07efc592f" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01224.x/asset/image_n/avsc1224-toc-0001.gif?v=1&amp;s=0bf8c03f3a0c048061f4c992f6cc07af5e893266"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Soil alkalization of the pine forest's in northern Estonia caused by cement kiln dust pollution has induced a succession from typical boreal vegetation toward vegetation of boreo-nemoral habitats. The establishment of calcicolous species shows their lack of dispersal limitation; species filtering success is determined by a critical level at the one end of the niche breath along the limiting gradient.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How resilient is boreal forest vegetation growing on acidic podzols to the environmental change caused by alkaline kiln dust pollution? How adaptive is the vegetation, when species pool and time for dispersal do not limit? How constant is the species niche breadth along the soil pH gradient?


Location
Region of 30 km around the Kunda cement plant, northern Estonia (59°30′ N, 26°32′ E), which has been continuously polluted last 140 years.


Methods
We sampled 20 forest stands on sandy gleyic podzols at various distances from the pollution source, leeward and windward of prevailing winds. Data processing: principal components analysis for gradient generalization, indicator species analysis for grouping species along the pollution gradient and generalized linear model analyses to estimate species reaction to pollution, considering covariates.


Results
The impact of alkaline dust accumulated over a century persisted despite resolute reductions of pollution. Forest soil conditions changed 10 km leeward and 5 km windward from the source: the litter pH level changed from 3.6 to 4.5 in unpolluted forests to 7.1–7.4 in the heavily polluted forests, and soil Ca content increased ten-fold. Soil alkalization has induced a remarkable succession from typical boreal vegetation toward vegetation of boreo-nemoral or calcareous habitats. We detected a linear increase of species richness from habitats on acidic soils (unpolluted) to newly formed alkaline soils (polluted habitats), reflecting the species pool composition and size, which is known to be large for calcicolous species. The establishment of several endangered calcicolous species shows the lack of dispersal limitation and points on their narrow soil pH niche. The niche breadth of species along the pH gradient varied among species, but only a few species appeared to be pH generalists.


Conclusions
Species ranking along the pH and/or Ca gradients indicates (1) the existence of different ecological guilds in terms of ecological niche use, and (2) the formation of a new community is dictated by the tolerance level of each species. This supports the individualistic community assembly rule suggested by Gleason. We find that such polluted regions with disturbed communities have high scientific value as long-term ecological experiments, but this might lead to conflict between the peculiar biodiversity complex and human well-being.

Soil alkalization of the pine forest's in northern Estonia caused by cement kiln dust pollution has induced a succession from typical boreal vegetation toward vegetation of boreo-nemoral habitats. The establishment of calcicolous species shows their lack of dispersal limitation; species filtering success is determined by a critical level at the one end of the niche breath along the limiting gradient.





</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01218.x" xmlns="http://purl.org/rss/1.0/"><title>Deforestation and precipitation patterns in the arid Chaco forests of central Argentina</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01218.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Deforestation and precipitation patterns in the arid Chaco forests of central Argentina</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">L.E. Hoyos, A.M. Cingolani, M.R. Zak, M.V. Vaieretti, D.E. Gorla, M.R. Cabido</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-09T02:59:39.139167-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01218.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01218.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01218.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">260</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">271</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1218-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Aims</h4><div class="para"><p>(1) to compare two series of precipitation data from different periods (1930–1950 and 1950–2000) in three sectors of the southern dry Chaco in the arid and semi-arid sub-regions; (2) construct maps showing the distribution of land-cover units for 1979, 1999, 2004 and 2010 for the same three sectors; and (3) assess the changes in land-cover units occurred between 1979 and 2010 in the three sectors.</p></div></div>
<div class="section" id="avsc1218-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Southern extreme of the dry Chaco in NE and NW Córdoba Province, central Argentina.</p></div></div>
<div class="section" id="avsc1218-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We compared annual and growth period (November–March) precipitation among the three sectors and between two series of data corresponding to different periods (1930–1950 and 1950–2000) using repeated measures ANOVA, with the station as the subject variable, period as the within-factor and sector as the between factor. Using three Landsat MSS (1979) and nine Landsat TM (1999, 2004 and 2010) images we mapped the distribution of eight land-cover units for the whole study area. For each sector (NE, NW and W), we performed a change detection analysis between 1979 and 2010.</p></div></div>
<div class="section" id="avsc1218-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The classification of Landsat MSS and TM images resulted in reliable land-cover maps (overall accuracy 80%). Our results showed that vegetation cover in the area is highly disturbed and that the present status of vegetation cover differs among the three sectors. In the more humid sector, the land-cover changes have been dominated by replacement of closed forests by crops, while in the driest portion of the study area forest loss was not related to agriculture. Additionally, we found that significant increases in precipitation have occurred in all three sectors, but the increase was highest in the humid sector.</p></div></div>
<div class="section" id="avsc1218-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The differences observed among the three sectors suggest that precipitation may have effectively played a dominant role in the process of forest conversion to agriculture.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01218.x/asset/image_m/avsc1218-toc-0001-m.png?v=1&amp;s=b21bcf689a909e64a816ade8302f03f909b06203" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01218.x/asset/image_n/avsc1218-toc-0001.gif?v=1&amp;s=bfc7dee1a215690c2a02e0d3f2c8c7479ffb3b5e"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The vegetation cover in the study area is highly disturbed. In the humid sector the land cover changes have been dominated by a replacement of closed forests by crops, while in the driest, forest loss was not related to agriculture. The significant increases in precipitation have occurred in the three sectors but in the humid one, the increase was highest.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Aims
(1) to compare two series of precipitation data from different periods (1930–1950 and 1950–2000) in three sectors of the southern dry Chaco in the arid and semi-arid sub-regions; (2) construct maps showing the distribution of land-cover units for 1979, 1999, 2004 and 2010 for the same three sectors; and (3) assess the changes in land-cover units occurred between 1979 and 2010 in the three sectors.


Location
Southern extreme of the dry Chaco in NE and NW Córdoba Province, central Argentina.


Methods
We compared annual and growth period (November–March) precipitation among the three sectors and between two series of data corresponding to different periods (1930–1950 and 1950–2000) using repeated measures ANOVA, with the station as the subject variable, period as the within-factor and sector as the between factor. Using three Landsat MSS (1979) and nine Landsat TM (1999, 2004 and 2010) images we mapped the distribution of eight land-cover units for the whole study area. For each sector (NE, NW and W), we performed a change detection analysis between 1979 and 2010.


Results
The classification of Landsat MSS and TM images resulted in reliable land-cover maps (overall accuracy 80%). Our results showed that vegetation cover in the area is highly disturbed and that the present status of vegetation cover differs among the three sectors. In the more humid sector, the land-cover changes have been dominated by replacement of closed forests by crops, while in the driest portion of the study area forest loss was not related to agriculture. Additionally, we found that significant increases in precipitation have occurred in all three sectors, but the increase was highest in the humid sector.


Conclusions
The differences observed among the three sectors suggest that precipitation may have effectively played a dominant role in the process of forest conversion to agriculture.

The vegetation cover in the study area is highly disturbed. In the humid sector the land cover changes have been dominated by a replacement of closed forests by crops, while in the driest, forest loss was not related to agriculture. The significant increases in precipitation have occurred in the three sectors but in the humid one, the increase was highest.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01216.x" xmlns="http://purl.org/rss/1.0/"><title>Urban grassland restoration: which plant traits make desired species successful colonizers?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01216.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Urban grassland restoration: which plant traits make desired species successful colonizers?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leonie K. Fischer, Moritz Lippe, Ingo Kowarik</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-02T06:15:27.344422-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01216.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01216.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01216.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">272</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">285</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1216-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>Which plant traits characterize successful and failed target species in urban grassland restoration? Do traits of successful target species differ from those of resident species? How do plant traits relate to environmental constraints?</p></div></div>
<div class="section" id="avsc1216-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>
<em>In-situ</em> experimental sites on wastelands in shrinking residential areas in Berlin, Germany.</p></div></div>
<div class="section" id="avsc1216-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We established grassland restoration treatments and explored plant traits of successful and failed target species (plant height, specific leaf area, seed mass, seed shape, seed longevity index, CSR strategy type, plant life form). To shed light on mechanisms that shape restoration success, we also analysed the same traits of species originating from the soil seed bank and species immigrating from the surroundings. We compared both trait sets to those of resident species. With RLQ analyses we related the trait data to abundance data of species and to variables describing the environmental setting of the sites.</p></div></div>
<div class="section" id="avsc1216-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>In the third year after treatment, several plant traits differed between the successful or failed target species and the resident vegetation, e.g. successful target species tended to be as tall as resident species, whereas failed target species were smaller, suggesting insufficient competitive ability of the latter. Species that successfully recruited from the soil seed bank were taller than resident species. Small specific leaf area was important for the establishment success of target species. Trait composition of the species assemblage clearly related to the environmental setting: mean specific leaf area and the proportion of annuals increased and the proportion of C-strategists decreased with increasing human-mediated impacts on the restoration sites.</p></div></div>
<div class="section" id="avsc1216-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Our results reveal clear trait differences between successful and failed target species in grassland restoration on urban wasteland sites, demonstrating that high competitive ability is crucial for success in target species. Grassland species that are successfully integrated into urban wasteland vegetation may thus fill well-defined vacant niches, while resembling the traits of the resident species in other ways. Our results may allow generalizations and transfer to similar urban settings, as the analysed trait states were assessed as relative values compared to resident species.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01216.x/asset/image_m/avsc1216-toc-0001-m.png?v=1&amp;s=5890916dcde08ca6e5e470edfe081941c243baef" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01216.x/asset/image_n/avsc1216-toc-0001.gif?v=1&amp;s=e543c28fdd6e98d6584f0e6e14d824d023f8c426"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Analysing trait composition of target and spontaneous species in grassland restoration on urban wastelands, we reveal clear differences between successful and failed target species (e.g., plant height). In comparison to resident and soil seed bank species, target species partially fill vacant niches, but also resemble traits of spontaneous species. High competitive ability is crucial for establishment success in target species.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
Which plant traits characterize successful and failed target species in urban grassland restoration? Do traits of successful target species differ from those of resident species? How do plant traits relate to environmental constraints?


Location

In-situ experimental sites on wastelands in shrinking residential areas in Berlin, Germany.


Methods
We established grassland restoration treatments and explored plant traits of successful and failed target species (plant height, specific leaf area, seed mass, seed shape, seed longevity index, CSR strategy type, plant life form). To shed light on mechanisms that shape restoration success, we also analysed the same traits of species originating from the soil seed bank and species immigrating from the surroundings. We compared both trait sets to those of resident species. With RLQ analyses we related the trait data to abundance data of species and to variables describing the environmental setting of the sites.


Results
In the third year after treatment, several plant traits differed between the successful or failed target species and the resident vegetation, e.g. successful target species tended to be as tall as resident species, whereas failed target species were smaller, suggesting insufficient competitive ability of the latter. Species that successfully recruited from the soil seed bank were taller than resident species. Small specific leaf area was important for the establishment success of target species. Trait composition of the species assemblage clearly related to the environmental setting: mean specific leaf area and the proportion of annuals increased and the proportion of C-strategists decreased with increasing human-mediated impacts on the restoration sites.


Conclusions
Our results reveal clear trait differences between successful and failed target species in grassland restoration on urban wasteland sites, demonstrating that high competitive ability is crucial for success in target species. Grassland species that are successfully integrated into urban wasteland vegetation may thus fill well-defined vacant niches, while resembling the traits of the resident species in other ways. Our results may allow generalizations and transfer to similar urban settings, as the analysed trait states were assessed as relative values compared to resident species.

Analysing trait composition of target and spontaneous species in grassland restoration on urban wastelands, we reveal clear differences between successful and failed target species (e.g., plant height). In comparison to resident and soil seed bank species, target species partially fill vacant niches, but also resemble traits of spontaneous species. High competitive ability is crucial for establishment success in target species.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12001" xmlns="http://purl.org/rss/1.0/"><title>Plant seedlings in a species-rich meadow: effect of management, vegetation type and functional traits</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12001</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Plant seedlings in a species-rich meadow: effect of management, vegetation type and functional traits</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ondřej Mudrák, Jiří Doležal, Michal Hájek, Martin Dančák, Leoš Klimeš, Jitka Klimešová</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-04T22:41:38.51964-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12001</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12001</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12001</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">286</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">295</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12001-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>(1) How do various mowing regimes used for the preservation of diverse meadow biota affect the occurrence of plant seedlings? (2) Does the effect of mowing regime on seedlings differ among vegetation types? (3) Are the seedlings occurring under a particular management type characterized by distinct functional traits? (4) Do the traits of seedlings differ from those of resident adult plant species?</p></div></div>
<div class="section" id="avsc12001-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>White Carpathians (Bílé Karpaty) Mountains, Czech Republic.</p></div></div>
<div class="section" id="avsc12001-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>In a species-rich meadow, seedlings (non-graminoids only) were identified to species and counted in an experiment that included management cessation and five mowing regimes in three types of vegetation for 2 yr. The abundance-weighted averages of functional traits were compared between seedling and adult plant communities.</p></div></div>
<div class="section" id="avsc12001-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Seedling occurrence was suppressed by management cessation (abandonment) but differences among the five mowing treatments were small for all vegetation types. Seedling density and species richness were highest in vegetation dominated by <em>Bromus erectus</em>, intermediate in vegetation dominated by <em>Molinia arundinacea</em>, and lowest in vegetation dominated by <em>Calamagrostis epigejos</em>. Comparison of functional trait composition of seedlings with that of adult plants revealed that seedlings were largely produced by species with no or limited clonal growth and with low stature, and therefore with lower competitive ability.</p></div></div>
<div class="section" id="avsc12001-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The results indicate that short-term alteration of the mowing regime does not change conditions conducive to seedling occurrence, but even short-term abandonment hinders the establishment of small, non-clonal species. Rapid changes in species composition after abandonment in temperate meadows are therefore due not only to competitive exclusion of subordinate plant species, but also to their inability to establish from seeds.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12001/asset/image_m/avsc12001-toc-0001-m.png?v=1&amp;s=9585ff1378cc987484941a04fad3c1316fe89162" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12001/asset/image_n/avsc12001-toc-0001.gif?v=1&amp;s=40ac6605ffd809029c32e59f8fdec54a71344095"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We assessed number and identity of forb seedlings in species rich meadow after two years of various management. Number of plant seedling species was substantially suppressed after the management cessation. Plants producing seedlings were non-clonals threatened by abandonment and plants without seedlings were clonal dominants. Hindered generative regeneration was proposed as responsible for species decline after meadow abandonment.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
(1) How do various mowing regimes used for the preservation of diverse meadow biota affect the occurrence of plant seedlings? (2) Does the effect of mowing regime on seedlings differ among vegetation types? (3) Are the seedlings occurring under a particular management type characterized by distinct functional traits? (4) Do the traits of seedlings differ from those of resident adult plant species?


Location
White Carpathians (Bílé Karpaty) Mountains, Czech Republic.


Methods
In a species-rich meadow, seedlings (non-graminoids only) were identified to species and counted in an experiment that included management cessation and five mowing regimes in three types of vegetation for 2 yr. The abundance-weighted averages of functional traits were compared between seedling and adult plant communities.


Results
Seedling occurrence was suppressed by management cessation (abandonment) but differences among the five mowing treatments were small for all vegetation types. Seedling density and species richness were highest in vegetation dominated by Bromus erectus, intermediate in vegetation dominated by Molinia arundinacea, and lowest in vegetation dominated by Calamagrostis epigejos. Comparison of functional trait composition of seedlings with that of adult plants revealed that seedlings were largely produced by species with no or limited clonal growth and with low stature, and therefore with lower competitive ability.


Conclusions
The results indicate that short-term alteration of the mowing regime does not change conditions conducive to seedling occurrence, but even short-term abandonment hinders the establishment of small, non-clonal species. Rapid changes in species composition after abandonment in temperate meadows are therefore due not only to competitive exclusion of subordinate plant species, but also to their inability to establish from seeds.

We assessed number and identity of forb seedlings in species rich meadow after two years of various management. Number of plant seedling species was substantially suppressed after the management cessation. Plants producing seedlings were non-clonals threatened by abandonment and plants without seedlings were clonal dominants. Hindered generative regeneration was proposed as responsible for species decline after meadow abandonment.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01217.x" xmlns="http://purl.org/rss/1.0/"><title>Effects of grasses on sapling establishment and the role of transplanted saplings on the light environment of pastures: implications for tropical forest restoration</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01217.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effects of grasses on sapling establishment and the role of transplanted saplings on the light environment of pastures: implications for tropical forest restoration</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paula Meli, Rodolfo Dirzo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-05T05:07:39.694585-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01217.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01217.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01217.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">296</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">304</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1217-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Does the presence of grasses affect the establishment (survival and growth) of tree saplings in an abandoned tropical pasture, and what is the potential of established saplings to modify pasture microenvironmental conditions, particularly light incidence?</p></div></div>
<div class="section" id="avsc1217-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Abandoned cattle pasture, in the humid tropics of SE Mexico (18°25′–18°45′ N, 95°00′–95°18′ W).</p></div></div>
<div class="section" id="avsc1217-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>The establishment of four native fast-growing tree species in a tropical abandoned pasture was evaluated. Saplings of <em>
Cecropia obtusifolia</em>,<em> Hampea nutricia</em>,<em> Omphalea oleifera</em> and <em>
Erythrina folkersii</em> were transplanted using a split-plot design. Plant survival and growth were evaluated over 12 mo under two experimental treatments: presence and absence of grasses. Light incidence at ground level was used to evaluate microclimate conditions under the grass matrix, compared to light incidence under saplings established in the pasture.</p></div></div>
<div class="section" id="avsc1217-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Saplings had high survival (49–88%) regardless of the presence of grasses. In the presence of grasses, growth of surviving saplings either increased or was not impacted, and in only one out of eight comparisons did grasses negatively affect growth. The impact of saplings on light incidence in abandoned pastures depended on sapling species architecture: species with large total leaf area and canopy area (<em>
H. nutricia</em> and <em>
E. folkersii</em>) significantly reduced light incidence (12–29% of total incidence), while narrow-canopy species (<em>
C. obtusifolia</em> and <em>
O. oleifera</em>) generated less intense shade (37–89% of total incidence).</p></div></div>
<div class="section" id="avsc1217-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Grasses did not seem to represent a crucial limiting factor in sapling establishment of fast-growing native species in the short term. In addition, shading by recruited saplings of some native species could be important to out-compete grasses in the future, as well as for ‘facilitating’ regeneration of more shade-tolerant species. Transplantation of fast-growing native saplings into abandoned pastures, even without manipulation of the grasses, could be a useful practice for landscape-scale restoration programmes in tropical areas. Evaluation of the longer-term consequences (beyond the 1-yr span of this study) warrants further research.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01217.x/asset/image_m/avsc1217-toc-0001-m.png?v=1&amp;s=201dafd2c9a2a535980531a2b38e2de27b456765" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01217.x/asset/image_n/avsc1217-toc-0001.gif?v=1&amp;s=bf7ef6f19cc3c5c79a909defd51b2906c6204a96"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We evaluated the effects of grasses on the establishment of four fast-growth tree saplings in a Neotropical abandoned pasture, and the potential of saplings to modify light incidence. Grasses did not seem to represent a limiting factor in sapling establishment in the short term. Shading by recruited saplings could be important to outcompete grasses and therefore ‘facilitate’ more shade-tolerant species.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Does the presence of grasses affect the establishment (survival and growth) of tree saplings in an abandoned tropical pasture, and what is the potential of established saplings to modify pasture microenvironmental conditions, particularly light incidence?


Location
Abandoned cattle pasture, in the humid tropics of SE Mexico (18°25′–18°45′ N, 95°00′–95°18′ W).


Methods
The establishment of four native fast-growing tree species in a tropical abandoned pasture was evaluated. Saplings of 
Cecropia obtusifolia, Hampea nutricia, Omphalea oleifera and 
Erythrina folkersii were transplanted using a split-plot design. Plant survival and growth were evaluated over 12 mo under two experimental treatments: presence and absence of grasses. Light incidence at ground level was used to evaluate microclimate conditions under the grass matrix, compared to light incidence under saplings established in the pasture.


Results
Saplings had high survival (49–88%) regardless of the presence of grasses. In the presence of grasses, growth of surviving saplings either increased or was not impacted, and in only one out of eight comparisons did grasses negatively affect growth. The impact of saplings on light incidence in abandoned pastures depended on sapling species architecture: species with large total leaf area and canopy area (
H. nutricia and 
E. folkersii) significantly reduced light incidence (12–29% of total incidence), while narrow-canopy species (
C. obtusifolia and 
O. oleifera) generated less intense shade (37–89% of total incidence).


Conclusions
Grasses did not seem to represent a crucial limiting factor in sapling establishment of fast-growing native species in the short term. In addition, shading by recruited saplings of some native species could be important to out-compete grasses in the future, as well as for ‘facilitating’ regeneration of more shade-tolerant species. Transplantation of fast-growing native saplings into abandoned pastures, even without manipulation of the grasses, could be a useful practice for landscape-scale restoration programmes in tropical areas. Evaluation of the longer-term consequences (beyond the 1-yr span of this study) warrants further research.

We evaluated the effects of grasses on the establishment of four fast-growth tree saplings in a Neotropical abandoned pasture, and the potential of saplings to modify light incidence. Grasses did not seem to represent a limiting factor in sapling establishment in the short term. Shading by recruited saplings could be important to outcompete grasses and therefore ‘facilitate’ more shade-tolerant species.






</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01225.x" xmlns="http://purl.org/rss/1.0/"><title>Co-variation between plant above-ground biomass and phenology in sub-alpine grasslands</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01225.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Co-variation between plant above-ground biomass and phenology in sub-alpine grasslands</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Antoine Duparc, Claire Redjadj, Flore Viard-Crétat, Sandra Lavorel, Gunnar Austrheim, Anne Loison</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-21T02:56:20.562048-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01225.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01225.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01225.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">305</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">316</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1225-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Resources quality and quantity are both important determinants of habitat use for large herbivores. We aim to understand how these two variables vary throughout the growing season in sub-alpine grasslands. How do productivity and phenology (quality) of different plant communities within a landscape vary over time? Do productivity and phenology co-vary? Which environmental constraints or growth form composition best explain differences in productivity and phenology among plant communities?</p></div></div>
<div class="section" id="avsc1225-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Calcareous sub-alpine grasslands, the external Alps, France.</p></div></div>
<div class="section" id="avsc1225-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We assessed how productivity (above-ground biomass) and phenology varied with date, slope, radiation and altitude among seven plant communities. Then we explored (1) co-variation among maximum biomass, the date of maximum biomass and average community flowering date for each plant community, and (2) whether these variables were related to snow regime or growth form composition.</p></div></div>
<div class="section" id="avsc1225-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Temporal dynamics of biomass and phenology varied markedly among plant communities. More productive communities reached their maximum biomass later. Flowering occurred after the biomass peak, except for one plant community. However, the later the biomass peak, the shorter the lag to flowering peak. The timing of flowering and date of maximum biomass were best explained by differences in snow regimes among communities. The impact of growth form composition was marginal.</p></div></div>
<div class="section" id="avsc1225-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Plant communities are under strong time constraints to grow and flower. Snowmelt regime plays a crucial role at one end of the growing season, while time left for fruiting and maturing is likely to influence the other end. Sub-alpine grassland communities are highly heterogeneous in productivity, timing of maximum productivity and flowering phenology, creating small-scale variability in the forage quality and quantity available to large herbivores.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01225.x/asset/image_m/avsc1225-toc-0001-m.png?v=1&amp;s=6ed878ea27f8fb0fe77a39dec6d31a282e9a7703" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01225.x/asset/image_n/avsc1225-toc-0001.gif?v=1&amp;s=c55a13ac02e679bf764bd136ef0717cfa57b776e"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Covariation between phenology and temporal biomass dynamics at plant community level may be important criteria of resource selection for upper trophic levels. In subalpine grasslands, flowering, followed maximum productivity but with a shorter lag the later the peak of productivity. Snow regime explained when biomass peaked but the end of the growing season imposed a constraint on flowering dates. Picture by Marc Cornillon.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Resources quality and quantity are both important determinants of habitat use for large herbivores. We aim to understand how these two variables vary throughout the growing season in sub-alpine grasslands. How do productivity and phenology (quality) of different plant communities within a landscape vary over time? Do productivity and phenology co-vary? Which environmental constraints or growth form composition best explain differences in productivity and phenology among plant communities?


Location
Calcareous sub-alpine grasslands, the external Alps, France.


Methods
We assessed how productivity (above-ground biomass) and phenology varied with date, slope, radiation and altitude among seven plant communities. Then we explored (1) co-variation among maximum biomass, the date of maximum biomass and average community flowering date for each plant community, and (2) whether these variables were related to snow regime or growth form composition.


Results
Temporal dynamics of biomass and phenology varied markedly among plant communities. More productive communities reached their maximum biomass later. Flowering occurred after the biomass peak, except for one plant community. However, the later the biomass peak, the shorter the lag to flowering peak. The timing of flowering and date of maximum biomass were best explained by differences in snow regimes among communities. The impact of growth form composition was marginal.


Conclusions
Plant communities are under strong time constraints to grow and flower. Snowmelt regime plays a crucial role at one end of the growing season, while time left for fruiting and maturing is likely to influence the other end. Sub-alpine grassland communities are highly heterogeneous in productivity, timing of maximum productivity and flowering phenology, creating small-scale variability in the forage quality and quantity available to large herbivores.

Covariation between phenology and temporal biomass dynamics at plant community level may be important criteria of resource selection for upper trophic levels. In subalpine grasslands, flowering, followed maximum productivity but with a shorter lag the later the peak of productivity. Snow regime explained when biomass peaked but the end of the growing season imposed a constraint on flowering dates. Picture by Marc Cornillon.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12000" xmlns="http://purl.org/rss/1.0/"><title>Vegetation phenology can be captured with digital repeat photography and linked to variability of root nutrition in Hedysarum alpinum</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12000</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Vegetation phenology can be captured with digital repeat photography and linked to variability of root nutrition in Hedysarum alpinum</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">W. Nijland, N.C. Coops, S.C.P. Coogan, C.W. Bater, M.A. Wulder, S.E. Nielsen, G. McDermid, G.B. Stenhouse</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-24T21:10:28.035612-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12000</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12000</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12000</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">317</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">324</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12000-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Can repeat (time-lapse) photography be used to detect the phenological development of a forest stand, and linked to temporal patterns in root nutrition for <em>Hedysarum alpinum</em> (alpine sweetvetch) an important grizzly bear food species?</p></div></div>
<div class="section" id="avsc12000-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Eastern foothills and front ranges of the Rocky Mountains in Alberta, Canada. The area contains a diverse mix of mature and young forest, wetlands and alpine habitats.</p></div></div>
<div class="section" id="avsc12000-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>We deployed six automated cameras at three locations to acquire daily photographs at the plant and forest stand scales. Plot locations were also visited on a bi-weekly basis to record the phenological stage of <em>H. alpinum</em> and other target plant species, as well as to collect a root sample for determination of crude protein content.</p></div></div>
<div class="section" id="avsc12000-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Repeat photography and image analysis successfully detected all key phenological events (i.e. green-up, flowering, senescence). Given the relation between phenology and root nutrition, we illustrate how camera data can be used to predict the spatial and temporal distribution and quality of a key wildlife resource.</p></div></div>
<div class="section" id="avsc12000-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Repeat photography provides a cost-effective method for monitoring vegetation development, food availability, and nutritional quality at a forest stand scale. Since wildlife responds to the availability and quality of their food resources, detailed information on changes in resource availability helps with land-use management decisions and furthers our understanding of grizzly bear feeding ecology and habitat selection.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12000/asset/image_m/avsc12000-toc-0001-m.png?v=1&amp;s=2b6d4d1557e12ba100bd0a73b95e7c0821a681e7" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12000/asset/image_n/avsc12000-toc-0001.gif?v=1&amp;s=bb5416023ebf0f374f0a7612484bef0792338e50"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Repeat photography can reliably detect the phenological development of <em>Hedysarum alpinum,</em> an important grizzly bear food species in the foothills and front ranges of the Rocky Mountains in Alberta, Canada. Through the relation between phenology and root nutrition, we illustrate how camera data can be used to predict the spatial and temporal distribution and quality of a key wildlife resource.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Can repeat (time-lapse) photography be used to detect the phenological development of a forest stand, and linked to temporal patterns in root nutrition for Hedysarum alpinum (alpine sweetvetch) an important grizzly bear food species?


Location
Eastern foothills and front ranges of the Rocky Mountains in Alberta, Canada. The area contains a diverse mix of mature and young forest, wetlands and alpine habitats.


Methods
We deployed six automated cameras at three locations to acquire daily photographs at the plant and forest stand scales. Plot locations were also visited on a bi-weekly basis to record the phenological stage of H. alpinum and other target plant species, as well as to collect a root sample for determination of crude protein content.


Results
Repeat photography and image analysis successfully detected all key phenological events (i.e. green-up, flowering, senescence). Given the relation between phenology and root nutrition, we illustrate how camera data can be used to predict the spatial and temporal distribution and quality of a key wildlife resource.


Conclusions
Repeat photography provides a cost-effective method for monitoring vegetation development, food availability, and nutritional quality at a forest stand scale. Since wildlife responds to the availability and quality of their food resources, detailed information on changes in resource availability helps with land-use management decisions and furthers our understanding of grizzly bear feeding ecology and habitat selection.

Repeat photography can reliably detect the phenological development of Hedysarum alpinum, an important grizzly bear food species in the foothills and front ranges of the Rocky Mountains in Alberta, Canada. Through the relation between phenology and root nutrition, we illustrate how camera data can be used to predict the spatial and temporal distribution and quality of a key wildlife resource.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01223.x" xmlns="http://purl.org/rss/1.0/"><title>Leaf functional traits for the assessment of succession following management in semi-natural grasslands: a case study in the North Apennines, Italy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01223.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Leaf functional traits for the assessment of succession following management in semi-natural grasslands: a case study in the North Apennines, Italy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stefano Targetti, Alessandro Messeri, Nicolina Staglianò, Giovanni Argenti</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-09T05:10:44.699306-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01223.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01223.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01223.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">325</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">332</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1223-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Question</h4><div class="para"><p>Do leaf functional traits describe variation in the intensity of management in semi-natural grasslands?</p></div></div>
<div class="section" id="avsc1223-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Mugello, North Apennines, Italy.</p></div></div>
<div class="section" id="avsc1223-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>In an ecologically homogeneous area, we identified four grassland management practices (three different stocking rates and abandonment for 10 or more years). We measured leaf functional traits (LFT) of three dominant grass species – leaf dry matter content (LDMC), specific leaf area (SLA) and leaf N concentration (LNC) – in two permanent sampling plots per treatment for two consecutive years. Statistical tests and multivariate analysis were employed to compare the traits and analyse their sensitivity in responding to the different management intensities.</p></div></div>
<div class="section" id="avsc1223-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The robustness of LDMC and SLA in grass species ranking was confirmed. Weighted LDMC and SLA were able to differentiate the most intensely managed site from the others.</p></div></div>
<div class="section" id="avsc1223-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The results of the weighted LDMC and the weighted SLA encourage further studies aimed at the development of a LFT database for the most common grass species of Apennine semi-natural grasslands. This could be of great help in the development of indicators able to support the formulation of rational management plans for conservation and sustainable animal production.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01223.x/asset/image_m/avsc1223-toc-0001-m.png?v=1&amp;s=6df39eea36fb4b393f226b47fe4d4411d35cd278" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01223.x/asset/image_n/avsc1223-toc-0001.gif?v=1&amp;s=52941a6475c15a58038ff80560275d657094289a"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We identified four grassland sites in similar ecological conditions and under different management practices for ten or more years. Weighted Leaf Dry Matter Content, weighted Leaf Nitrogen Content and weighted Specific Leaf Area were able to differentiate the most intensely managed site from the others. Indicators based on leaf functional traits could aid the formulation of rational management plans.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Question
Do leaf functional traits describe variation in the intensity of management in semi-natural grasslands?


Location
Mugello, North Apennines, Italy.


Methods
In an ecologically homogeneous area, we identified four grassland management practices (three different stocking rates and abandonment for 10 or more years). We measured leaf functional traits (LFT) of three dominant grass species – leaf dry matter content (LDMC), specific leaf area (SLA) and leaf N concentration (LNC) – in two permanent sampling plots per treatment for two consecutive years. Statistical tests and multivariate analysis were employed to compare the traits and analyse their sensitivity in responding to the different management intensities.


Results
The robustness of LDMC and SLA in grass species ranking was confirmed. Weighted LDMC and SLA were able to differentiate the most intensely managed site from the others.


Conclusions
The results of the weighted LDMC and the weighted SLA encourage further studies aimed at the development of a LFT database for the most common grass species of Apennine semi-natural grasslands. This could be of great help in the development of indicators able to support the formulation of rational management plans for conservation and sustainable animal production.

We identified four grassland sites in similar ecological conditions and under different management practices for ten or more years. Weighted Leaf Dry Matter Content, weighted Leaf Nitrogen Content and weighted Specific Leaf Area were able to differentiate the most intensely managed site from the others. Indicators based on leaf functional traits could aid the formulation of rational management plans.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12002" xmlns="http://purl.org/rss/1.0/"><title>A methodological approach for assessing the effects of disturbance factors on the conservation status of Mediterranean coastal dune systems</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12002</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A methodological approach for assessing the effects of disturbance factors on the conservation status of Mediterranean coastal dune systems</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fabio Attorre, Alberto Maggini, Mario Di Traglia, Michele De Sanctis, Marcello Vitale</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-24T03:36:11.377136-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/avsc.12002</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/avsc.12002</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Favsc.12002</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">333</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">342</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc12002-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>How can the conservation status of Mediterranean coastal dunes be assessed? What is the effect of disturbance factors on it?</p></div></div>
<div class="section" id="avsc12002-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>Tyrrhenian coast of Central Italy.</p></div></div>
<div class="section" id="avsc12002-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Vegetation relevés along 164 transects lying perpendicular to the shoreline along the Tyrrhenian coast of Central Italy were used to identify the presence of dune habitats by means of TWINSPAN classification and detrended correspondence analysis. Multiple correspondence analysis was used to analyse relationship between habitats and disturbance factors. The resulting Burt's table was used to build an index (habitat-disturbance, HDi) for analysing this relationship. Based on HDi values, a correspondence analysis (CA) between presence/absence of habitats and disturbances was performed. The overall plant species diversity of dunes was measured with NH<sub>DUNE</sub>, a modified version of the Shannon index. Multi-way ANOVA procedure was used to investigate effect of single disturbance factors and their interactive effect on NH<sub>DUNE</sub>.</p></div></div>
<div class="section" id="avsc12002-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Classification and ordination procedures identified four sequential habitats moving from the shoreline to inland: annual vegetation on drift lines characterized by <em>Cakile maritima</em>; embryonic shifting dunes dominated by <em>Elymus farctus</em>; shifting dunes with <em>Ammophila arenaria</em> subsp. <em>australis</em>; back dune grasslands characterized by <em>Ononis variegata</em>. CA showed that disturbance factors influence dune habitats differently. In particular, the <em>Cakile</em> community had a negative relationship with beach tourism and mechanical cleaning; the <em>Elymus</em> community had a positive relationship with beach tourism and mechanical cleaning and a negative relationship with erosion and bathing establishments; the <em>Ammophila</em> community had a negative relationship with mechanical cleaning and bathing establishments and a positive relationship with dune cross-trampling; and the <em>Ononis</em> community had a negative relationship with bathing establishment. According to multi-way ANOVA, single disturbance factors can have different effects on plant species diversity as measured by NH<sub>DUNE</sub>. However, the overall effect is negative, with erosion as a single factor and the combination of mechanical cleaning and bathing establishments significantly lowering the plant diversity of coastal dune systems.</p></div></div>
<div class="section" id="avsc12002-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The proposed method allows a fast and replicable evaluation of the effects of disturbance factors on the conservation status of Mediterranean coastal dunes, providing the information necessary for development of conservation strategies focusing on a single habitat or on the overall dune system.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/avsc.12002/asset/image_m/avsc12002-toc-0001-m.png?v=1&amp;s=eadb8bdab5aa36dc6be5ba64e04665fc2a636783" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/avsc.12002/asset/image_n/avsc12002-toc-0001.gif?v=1&amp;s=4046a4d211131c33ca19199081d0d1181ce4acf2"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Mediterranean coastal dunes are threatened by human disturbances. For this reason the need for quantitatively assessing their conservation status and the effects of disturbance factors on them emerged. Our paper was aimed at evaluating the relationship between the presence of typical dune habitats and plant diversity indexes, and disturbance factors by means of Multiple Correspondence Analysis and multi-way ANOVA.
</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
How can the conservation status of Mediterranean coastal dunes be assessed? What is the effect of disturbance factors on it?


Location
Tyrrhenian coast of Central Italy.


Methods
Vegetation relevés along 164 transects lying perpendicular to the shoreline along the Tyrrhenian coast of Central Italy were used to identify the presence of dune habitats by means of TWINSPAN classification and detrended correspondence analysis. Multiple correspondence analysis was used to analyse relationship between habitats and disturbance factors. The resulting Burt's table was used to build an index (habitat-disturbance, HDi) for analysing this relationship. Based on HDi values, a correspondence analysis (CA) between presence/absence of habitats and disturbances was performed. The overall plant species diversity of dunes was measured with NHDUNE, a modified version of the Shannon index. Multi-way ANOVA procedure was used to investigate effect of single disturbance factors and their interactive effect on NHDUNE.


Results
Classification and ordination procedures identified four sequential habitats moving from the shoreline to inland: annual vegetation on drift lines characterized by Cakile maritima; embryonic shifting dunes dominated by Elymus farctus; shifting dunes with Ammophila arenaria subsp. australis; back dune grasslands characterized by Ononis variegata. CA showed that disturbance factors influence dune habitats differently. In particular, the Cakile community had a negative relationship with beach tourism and mechanical cleaning; the Elymus community had a positive relationship with beach tourism and mechanical cleaning and a negative relationship with erosion and bathing establishments; the Ammophila community had a negative relationship with mechanical cleaning and bathing establishments and a positive relationship with dune cross-trampling; and the Ononis community had a negative relationship with bathing establishment. According to multi-way ANOVA, single disturbance factors can have different effects on plant species diversity as measured by NHDUNE. However, the overall effect is negative, with erosion as a single factor and the combination of mechanical cleaning and bathing establishments significantly lowering the plant diversity of coastal dune systems.


Conclusions
The proposed method allows a fast and replicable evaluation of the effects of disturbance factors on the conservation status of Mediterranean coastal dunes, providing the information necessary for development of conservation strategies focusing on a single habitat or on the overall dune system.

Mediterranean coastal dunes are threatened by human disturbances. For this reason the need for quantitatively assessing their conservation status and the effects of disturbance factors on them emerged. Our paper was aimed at evaluating the relationship between the presence of typical dune habitats and plant diversity indexes, and disturbance factors by means of Multiple Correspondence Analysis and multi-way ANOVA.







</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01219.x" xmlns="http://purl.org/rss/1.0/"><title>Broad-scale satellite Normalized Difference Vegetation Index data predict plant biomass and peak date of nitrogen concentration in Arctic tundra vegetation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01219.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Broad-scale satellite Normalized Difference Vegetation Index data predict plant biomass and peak date of nitrogen concentration in Arctic tundra vegetation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Madeleine Doiron, Pierre Legagneux, Gilles Gauthier, Esther Lévesque</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-09T02:45:35.688654-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1654-109X.2012.01219.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1654-109X.2012.01219.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1654-109X.2012.01219.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">343</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">351</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="section" id="avsc1219-sec-0001" xmlns="http://www.w3.org/1999/xhtml"><h4>Questions</h4><div class="para"><p>Is the satellite-derived Normalized Difference Vegetation Index (NDVI) an adequate proxy for the timing of the peak in plant nitrogen concentration in an Arctic tundra system? Can NDVI be used to reliably assess seasonal changes in aboveground plant biomass?</p></div></div>
<div class="section" id="avsc1219-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Location</h4><div class="para"><p>The south plain of Bylot Island, an Arctic tundra ecosystem north of Baffin Island, Nunavut, Canada (73°08′ N, 80°00′ W).</p></div></div>
<div class="section" id="avsc1219-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Using plant data collected every 2 wk throughout the summer in 1991, 1993–1996 and 2006–2008, we assessed the relationship between four NDVI indices (AVHRR satellite data at 1-km<sup>2</sup> spatial resolution) and the date of peak nitrogen concentration in wetland graminoid plants, which represents seasonal variability in plant quality. We also examined the relationship between NDVI and the seasonal changes in aboveground live plant biomass.</p></div></div>
<div class="section" id="avsc1219-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Three out of the four NDVI metrics that we tested were significantly related to date of peak nitrogen concentration. The strongest relationship was found with the date at which NDVI values reached 50% of their annual maximum (<em>r</em><sup>2</sup> = 0.87). We also found a positive exponential relationship between NDVI and aboveground biomass of plants (<em>r</em><sup>2</sup> = 0.58), though this relationship was strongest early in the growing season.</p></div></div>
<div class="section" id="avsc1219-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>NDVI can be used as a proxy to determine date of peak nitrogen concentration in some tundra plants, and can thus be a reliable measure of the yearly changes in the timing of the availability of high quality food for herbivores. To a lesser extent, NDVI can also be used to assess seasonal change in plant biomass. This study provides additional support for the use of broad-scale satellite-derived NDVI to assess seasonal changes in habitat quality for herbivores.</p></div></div>
<a title="Link to full-size graphical abstract" class="figZoom" href="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01219.x/asset/image_m/avsc1219-toc-0001-m.png?v=1&amp;s=1946dd103d0390cf4825fa3db3d1f4d4a7cb697f" xmlns="http://www.w3.org/1999/xhtml"><img alt="Thumbnail image of graphical abstract" title="Thumbnail image of graphical abstract" src="http://onlinelibrary.wiley.com/store/10.1111/j.1654-109X.2012.01219.x/asset/image_n/avsc1219-toc-0001.gif?v=1&amp;s=7b9d0572f86f7c38656240d513163172b5b2c13b"/></a>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Using 8 yr of plant data, this study shows that satellite-derived NDVI can be a good proxy for aboveground biomass and the date of peak nitrogen concentration of wetland graminoid plants in an Arctic tundra system. We conclude that NDVI can be a reliable measure of seasonal changes in the timing and availability of high quality food for herbivores.</p><!--Unmatched element: w:blockFixed--></div>
]]></content:encoded><description>


Questions
Is the satellite-derived Normalized Difference Vegetation Index (NDVI) an adequate proxy for the timing of the peak in plant nitrogen concentration in an Arctic tundra system? Can NDVI be used to reliably assess seasonal changes in aboveground plant biomass?


Location
The south plain of Bylot Island, an Arctic tundra ecosystem north of Baffin Island, Nunavut, Canada (73°08′ N, 80°00′ W).


Methods
Using plant data collected every 2 wk throughout the summer in 1991, 1993–1996 and 2006–2008, we assessed the relationship between four NDVI indices (AVHRR satellite data at 1-km2 spatial resolution) and the date of peak nitrogen concentration in wetland graminoid plants, which represents seasonal variability in plant quality. We also examined the relationship between NDVI and the seasonal changes in aboveground live plant biomass.


Results
Three out of the four NDVI metrics that we tested were significantly related to date of peak nitrogen concentration. The strongest relationship was found with the date at which NDVI values reached 50% of their annual maximum (r2 = 0.87). We also found a positive exponential relationship between NDVI and aboveground biomass of plants (r2 = 0.58), though this relationship was strongest early in the growing season.


Conclusions
NDVI can be used as a proxy to determine date of peak nitrogen concentration in some tundra plants, and can thus be a reliable measure of the yearly changes in the timing of the availability of high quality food for herbivores. To a lesser extent, NDVI can also be used to assess seasonal change in plant biomass. This study provides additional support for the use of broad-scale satellite-derived NDVI to assess seasonal changes in habitat quality for herbivores.

Using 8 yr of plant data, this study shows that satellite-derived NDVI can be a good proxy for aboveground biomass and the date of peak nitrogen concentration of wetland graminoid plants in an Arctic tundra system. We conclude that NDVI can be a reliable measure of seasonal changes in the timing and availability of high quality food for herbivores.




</description></item></rdf:RDF>