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<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)1756-1051" xmlns="http://purl.org/rss/1.0/"><title>Nordic Journal of Botany</title><description> Wiley Online Library : Nordic Journal of Botany</description><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2F%28ISSN%291756-1051</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/">© Nordic Journal of Botany</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">0107-055X</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1756-1051</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">May 2013</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">31</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/">129</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">256</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/more.2013.31.issue-2/asset/cover.gif?v=1&amp;s=0f0b8f3a5505498742f31ae3c5090122cd8d4938"/><items><rdf:Seq><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00014.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00039.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00034.x"/><rdf:li 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xmlns="http://purl.org/rss/1.0/"><title> Centaurea shahuensis and C. ravansarensis spp. nov. (Asteraceae, Cardueae) from west Iran</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00014.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Centaurea shahuensis and C. ravansarensis spp. nov. (Asteraceae, Cardueae) from west Iran</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Massoud Ranjbar, Kazem Negaresh, Roya Karamian</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-23T07:49:09.62865-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.00014.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.1756-1051.2012.00014.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00014.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Two new species of <em>Centaurea</em> L. sect. <em>Cynaroides</em> Boiss. ex Walp. (Asteraceae), <em>C. shahuensis</em> Ranjbar and Negaresh and <em>C. ravansarensis</em> Ranjbar and Negaresh are described and illustrated from Kermanshah Province, west Iran. They are closely related to <em>C. regia</em> Boiss. subsp. <em>regia</em>. However, <em>C. shahuensis</em> differs from it by median stem leaves broadly oblanceolate or subpandurate, phyllaries densely lanate-tomentose, appendages small, concealing a minor part of phyllaries, and also median appendage margin entire sometimes with 1–2 cilia, 1.2–3.0 mm long on each side. <em>Centaurea ravansarensis</em> is distinguished by upper stem leaves loosely arachnoid, phyllaries loosely floccose-tomentose, inner appendages deep brown to blackish, and spine 4.5–6.0 mm long. Habitat, conservation status and the geographical distribution of the new species are given.</p></div>
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Two new species of Centaurea L. sect. Cynaroides Boiss. ex Walp. (Asteraceae), C. shahuensis Ranjbar and Negaresh and C. ravansarensis Ranjbar and Negaresh are described and illustrated from Kermanshah Province, west Iran. They are closely related to C. regia Boiss. subsp. regia. However, C. shahuensis differs from it by median stem leaves broadly oblanceolate or subpandurate, phyllaries densely lanate-tomentose, appendages small, concealing a minor part of phyllaries, and also median appendage margin entire sometimes with 1–2 cilia, 1.2–3.0 mm long on each side. Centaurea ravansarensis is distinguished by upper stem leaves loosely arachnoid, phyllaries loosely floccose-tomentose, inner appendages deep brown to blackish, and spine 4.5–6.0 mm long. Habitat, conservation status and the geographical distribution of the new species are given.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00039.x" xmlns="http://purl.org/rss/1.0/"><title> Elaphoglossum clathratum sp. nov. (Dryopteridaceae) from the eastern side of the Andes in Ecuador</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00039.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Elaphoglossum clathratum sp. nov. (Dryopteridaceae) from the eastern side of the Andes in Ecuador</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fernando B. Matos, Robbin C. Moran</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-20T05:30:27.056117-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.00039.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.1756-1051.2012.00039.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00039.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Elaphoglossum clathratum</em> F. B. Matos &amp; R. C. Moran sp. nov. (Dryopteridaceae), which grows at middle elevations on the eastern side of the Andes in Ecuador, is described, illustrated, and compared to its most similar species. It is unusual in <em>Elaphoglossum</em> by having lamina margin scales that are strongly clathrate. Research on the phylogeny of the genus has shown that the new species belongs to <em>Elaphoglossum</em> sect. <em>Polytrichia</em>. However, it is unique in the subulate-scaled clade of <em>Elaphoglossum</em> by having planar, not subulate, scales.</p></div>
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Elaphoglossum clathratum F. B. Matos &amp; R. C. Moran sp. nov. (Dryopteridaceae), which grows at middle elevations on the eastern side of the Andes in Ecuador, is described, illustrated, and compared to its most similar species. It is unusual in Elaphoglossum by having lamina margin scales that are strongly clathrate. Research on the phylogeny of the genus has shown that the new species belongs to Elaphoglossum sect. Polytrichia. However, it is unique in the subulate-scaled clade of Elaphoglossum by having planar, not subulate, scales.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00034.x" xmlns="http://purl.org/rss/1.0/"><title> Elatostema planinerve and E. longicuspe spp. nov. (Urticaceae) from Guizhou Province, China</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00034.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Elatostema planinerve and E. longicuspe spp. nov. (Urticaceae) from Guizhou Province, China</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fang Wen, Long-Fei Fu, Yi-Gang Wei, Wen-Tsai Wang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-13T12:02:48.538201-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.00034.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.1756-1051.2012.00034.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00034.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Two new species, <em>Elatostema planinerve</em> W. T. Wang &amp; Y. G. Wei sp. nov. and <em>E. longicuspe</em> W. T. Wang &amp; Y. G. Wei sp. nov. are described and illustrated from the Guizhou province, China. The former resembles <em>E. bracteosum</em> but differs in leaves, pistillate bracts and pistillate bracteoles; the latter is similar to <em>E. tenuicornutum</em>, but differs in stem surface, leaf shape, venation, cystoliths, staminate inflorescence bracts, bracteolate and staminate flowers.</p></div>
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Two new species, Elatostema planinerve W. T. Wang &amp; Y. G. Wei sp. nov. and E. longicuspe W. T. Wang &amp; Y. G. Wei sp. nov. are described and illustrated from the Guizhou province, China. The former resembles E. bracteosum but differs in leaves, pistillate bracts and pistillate bracteoles; the latter is similar to E. tenuicornutum, but differs in stem surface, leaf shape, venation, cystoliths, staminate inflorescence bracts, bracteolate and staminate flowers.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00057.x" xmlns="http://purl.org/rss/1.0/"><title> Didymocarpus dissectus sp. nov. (Gesneriaceae) from Fujian, eastern China</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00057.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Didymocarpus dissectus sp. nov. (Gesneriaceae) from Fujian, eastern China</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fang Wen, Yan-Lian Qiu, Jie Huang, Bo Zhao, Yi-Gang Wei</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-06T10:23:26.328831-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.00057.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.1756-1051.2012.00057.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00057.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>A new species of Gesneriaceae, <em>Didymocarpus dissectus</em> Fang Wen, Y. L. Qiu &amp; Y. G. Wei, from Fujian province, China, is described and illustrated. It is similar to <em>D. heucherifolius</em> in flower shape, but can be easily distinguished by leaf blade shape, split extent of calyx and equal calyx lobes, indumentum of corolla and number of staminodes.</p></div>
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A new species of Gesneriaceae, Didymocarpus dissectus Fang Wen, Y. L. Qiu &amp; Y. G. Wei, from Fujian province, China, is described and illustrated. It is similar to D. heucherifolius in flower shape, but can be easily distinguished by leaf blade shape, split extent of calyx and equal calyx lobes, indumentum of corolla and number of staminodes.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01628.x" xmlns="http://purl.org/rss/1.0/"><title>Three hawkweeds (Hieracium, Asteraceae) from the Netherlands typified and raised to species rank</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01628.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Three hawkweeds (Hieracium, Asteraceae) from the Netherlands typified and raised to species rank</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rense Haveman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-28T06:30:26.70584-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01628.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.1756-1051.2012.01628.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01628.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>After a short sketch of Dutch hieraciology, three taxa belonging to <em>Hieracium</em> sectt. <em>Vulgata</em> and <em>Tridentata</em> that were described from the Netherlands at the rank of subspecies or variety by Zahn are typified and raised to species rank. <em>Hieracium meppelense</em> (Zahn) Haveman comb. et stat nov. is found in the province of Drenthe in the northeastern part of the country, <em>H. limburgense</em> (Zahn) Haveman comb. et stat nov. in south-Limburg in the southernmost part and <em>H. macrodontophyllum</em> (Van Soest et Zahn) Haveman comb. et stat nov. in the surroundings of Nijmegen and Arnhem, and further north in the central sand area. Photographs of the types as well as maps with the hitherto known distribution of these three species are included.</p></div>
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After a short sketch of Dutch hieraciology, three taxa belonging to Hieracium sectt. Vulgata and Tridentata that were described from the Netherlands at the rank of subspecies or variety by Zahn are typified and raised to species rank. Hieracium meppelense (Zahn) Haveman comb. et stat nov. is found in the province of Drenthe in the northeastern part of the country, H. limburgense (Zahn) Haveman comb. et stat nov. in south-Limburg in the southernmost part and H. macrodontophyllum (Van Soest et Zahn) Haveman comb. et stat nov. in the surroundings of Nijmegen and Arnhem, and further north in the central sand area. Photographs of the types as well as maps with the hitherto known distribution of these three species are included.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01561.x" xmlns="http://purl.org/rss/1.0/"><title> Macromitrium ousiense, a neglected Chinese moss species (Orthotrichaceae, Bryopsida) with new synonym and records</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01561.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Macromitrium ousiense, a neglected Chinese moss species (Orthotrichaceae, Bryopsida) with new synonym and records</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jing Yu, Shui-Liang Guo, Yahong Ma, Tong Cao</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-28T06:29:14.533891-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01561.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.1756-1051.2012.01561.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01561.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Macromitrium ousiense</em> is a neglected Chinese moss species, differing from other taxa of the genus in its leaves with smooth laminal cells and gymnostomus capsules with hairy calyptrae. We found that <em>M. heterodictyon</em> Dixon is a new synonym of <em>M. ousiense</em>, and Japan is a new distribution record for the species.</p></div>
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Macromitrium ousiense is a neglected Chinese moss species, differing from other taxa of the genus in its leaves with smooth laminal cells and gymnostomus capsules with hairy calyptrae. We found that M. heterodictyon Dixon is a new synonym of M. ousiense, and Japan is a new distribution record for the species.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01674.x" xmlns="http://purl.org/rss/1.0/"><title>Two new polypores (Ceriporiopsis lavendula and Skeletocutis inflata spp. nov.) from Guangdong Province, China</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01674.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Two new polypores (Ceriporiopsis lavendula and Skeletocutis inflata spp. nov.) from Guangdong Province, China</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bao-Kai Cui</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-28T06:27:23.673294-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01674.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.1756-1051.2012.01674.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01674.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Two new polypores (<em>Ceriporiopsis lavendula</em> B. K. Cui sp. nov. and <em>Skeletocutis inflata</em> B. K. Cui sp. nov.) are described from the Guangdong Province in southern China. <em>Ceriporiopsis lavendula</em> is characterized by having resupinate basidiocarps with lavender to grayish blue pore surface and very thin to almost absent subiculum, a monomitic hyphal system with clamped generative hyphae, and oblong-ellipsoid to ellipsoid basidiospores. Moreover, it grows on wood of <em>Castanopsis</em> exclusively. <em>Skeletocutis inflata</em> is characterized by having pileate basidiocarps, smaller pores (8–10 per mm), inflated and partly dissolved skeletal hyphae in KOH. In addition, its tramal skeletal hyphae are parallel along the tubes. Identification keys to species of <em>Ceriporiopsis</em> and <em>Skeletocutis</em> occurring in China are provided.</p></div>
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Two new polypores (Ceriporiopsis lavendula B. K. Cui sp. nov. and Skeletocutis inflata B. K. Cui sp. nov.) are described from the Guangdong Province in southern China. Ceriporiopsis lavendula is characterized by having resupinate basidiocarps with lavender to grayish blue pore surface and very thin to almost absent subiculum, a monomitic hyphal system with clamped generative hyphae, and oblong-ellipsoid to ellipsoid basidiospores. Moreover, it grows on wood of Castanopsis exclusively. Skeletocutis inflata is characterized by having pileate basidiocarps, smaller pores (8–10 per mm), inflated and partly dissolved skeletal hyphae in KOH. In addition, its tramal skeletal hyphae are parallel along the tubes. Identification keys to species of Ceriporiopsis and Skeletocutis occurring in China are provided.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01620.x" xmlns="http://purl.org/rss/1.0/"><title>Nomenclatural notes on Rhododendron sparsifolium (Ericaceae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01620.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Nomenclatural notes on Rhododendron sparsifolium (Ericaceae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wen-Bin Yu, Fei He</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-28T06:25:22.281514-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01620.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.1756-1051.2012.01620.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01620.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Based on examination of original material, we demonstrate that the name <em>Rhododendron sparsifolium</em> W. P. Fang was indeed validly published when first published in 1983. Meanwhile, we correct the collectors of two of the three type gatherings listed in the protologue, including the holotype. Furthermore, we propose to reduce <em>R. hejiangense</em> to the synonymy of <em>R. sparsifolium</em> on the basis of morphological comparisons.</p></div>
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Based on examination of original material, we demonstrate that the name Rhododendron sparsifolium W. P. Fang was indeed validly published when first published in 1983. Meanwhile, we correct the collectors of two of the three type gatherings listed in the protologue, including the holotype. Furthermore, we propose to reduce R. hejiangense to the synonymy of R. sparsifolium on the basis of morphological comparisons.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00081.x" xmlns="http://purl.org/rss/1.0/"><title> Djinga cheekii sp. nov. (Podostemaceae) from Cameroon</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00081.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Djinga cheekii sp. nov. (Podostemaceae) from Cameroon</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jean-Paul Ghogue, Konrad A. Huber, Rolf Rutishauser</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T05:35:00.509385-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.00081.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.1756-1051.2012.00081.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00081.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>A new species is added to the monotypic African genus <em>Djinga. Djinga cheekii</em> Ghogue, Huber &amp; Rutish. (Podostemaceae) is described as a new species from Cameroon (Littoral Province) and its morphological affinities and conservation status are assessed. The main distinguishing characters are: stamens 2 (not 1 as in <em>D. felicis</em>), flower buds inside spathella strongly inclined (not only slightly inclined as in <em>D. felicis</em>), and stems lacking or only up to 6 mm long (not up to &gt; 6 cm as in <em>D. felicis</em>). A molecular analysis revealed that <em>D. cheekii</em> is sister to <em>D. felicis</em>, and both together are sister to <em>Ledermanniella linearifolia</em> and <em>L. pusilla</em> which show completely inverted flower buds inside the spathella, as typical for the large and still artificial genus <em>Ledermanniella.</em></p></div>
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A new species is added to the monotypic African genus Djinga. Djinga cheekii Ghogue, Huber &amp; Rutish. (Podostemaceae) is described as a new species from Cameroon (Littoral Province) and its morphological affinities and conservation status are assessed. The main distinguishing characters are: stamens 2 (not 1 as in D. felicis), flower buds inside spathella strongly inclined (not only slightly inclined as in D. felicis), and stems lacking or only up to 6 mm long (not up to &gt; 6 cm as in D. felicis). A molecular analysis revealed that D. cheekii is sister to D. felicis, and both together are sister to Ledermanniella linearifolia and L. pusilla which show completely inverted flower buds inside the spathella, as typical for the large and still artificial genus Ledermanniella.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01668.x" xmlns="http://purl.org/rss/1.0/"><title> Mouriri morleyii sp. nov. (Melastomataceae) from Brazil, with notes on its foliar stomatal crypts</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01668.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Mouriri morleyii sp. nov. (Melastomataceae) from Brazil, with notes on its foliar stomatal crypts</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Renato Goldenberg, Julia Meirelles, Erika Amano</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T05:32:29.011923-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01668.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.1756-1051.2012.01668.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01668.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Mouriri morleyii</em> R. Goldenb. &amp; Meirelles sp. nov. can be distinguished from the other species in the genus by its large stomatal crypts (the largest ones in the genus), columnar sclereids, tetramerous flowers and calyx closed in bud. This new species was collected on an inselberg in the state of Espírito Santo, Brazil.</p></div>
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Mouriri morleyii R. Goldenb. &amp; Meirelles sp. nov. can be distinguished from the other species in the genus by its large stomatal crypts (the largest ones in the genus), columnar sclereids, tetramerous flowers and calyx closed in bud. This new species was collected on an inselberg in the state of Espírito Santo, Brazil.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01619.x" xmlns="http://purl.org/rss/1.0/"><title> Rubia austrozhejiangensis sp. nov. (Rubiaceae) from Zhejiang, China</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01619.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Rubia austrozhejiangensis sp. nov. (Rubiaceae) from Zhejiang, China</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zu-Pei Lei, Ying-Ying Zhou, Rong-Wei Wang, Xiao-Feng Jin</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T05:30:35.419537-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01619.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.1756-1051.2012.01619.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01619.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Rubia austrozhejiangensis</em> Z. P. Lei, Y. Y. Zhou &amp; R. W. Wang, a new species of Rubiaceae from China, is described and illustrated. The new species is similar to <em>R. ovatifolia</em> Z. Ying Zhang and <em>R. argyi</em> (H. Lév. &amp; Vaniot) H. Hara ex Lauener, but differs from the former in having stems and branches cylindrical, not quadrate-angled, long-ovate to ovate-lanceolate leaf blades, many-flowered inflorescence, and smaller mericarps, 3–4 mm in diameter. In <em>R. ovatifolia</em>, stems and branches are quadrate-angled, leaf blades ovate, ovate-cordate to rounded cordate, and the inflorescences are sparsely flowered. Compared to <em>R. argyi</em>, the new species has cylindrical, not quadrate-angled stems and branches, leaf blades that are long-ovate to ovate-lanceolate, 3–5-veined, and slightly reflexed corolla lobes. In <em>R. argyi</em>, stems and branches are quadrate-angled or winged, the corolla lobes are spreading, and the mericarps are 5–7 mm in diameter.</p></div>
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Rubia austrozhejiangensis Z. P. Lei, Y. Y. Zhou &amp; R. W. Wang, a new species of Rubiaceae from China, is described and illustrated. The new species is similar to R. ovatifolia Z. Ying Zhang and R. argyi (H. Lév. &amp; Vaniot) H. Hara ex Lauener, but differs from the former in having stems and branches cylindrical, not quadrate-angled, long-ovate to ovate-lanceolate leaf blades, many-flowered inflorescence, and smaller mericarps, 3–4 mm in diameter. In R. ovatifolia, stems and branches are quadrate-angled, leaf blades ovate, ovate-cordate to rounded cordate, and the inflorescences are sparsely flowered. Compared to R. argyi, the new species has cylindrical, not quadrate-angled stems and branches, leaf blades that are long-ovate to ovate-lanceolate, 3–5-veined, and slightly reflexed corolla lobes. In R. argyi, stems and branches are quadrate-angled or winged, the corolla lobes are spreading, and the mericarps are 5–7 mm in diameter.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00009.x" xmlns="http://purl.org/rss/1.0/"><title>Species richness and endemicity in the Spanish vascular flora</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00009.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Species richness and endemicity in the Spanish vascular flora</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carlos Aedo, Leopoldo Medina, Marta Fernández-Albert</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-23T09:10:24.663662-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.00009.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.1756-1051.2012.00009.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00009.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Data from an updated and revised checklist of the Spanish flora is analyzed. The Spanish vascular plant flora is composed of 204 families, 1433 genera and 7071 species. Floristic data are analysed by considering three regions: mainland Spain with 5984 species, the Balearic Islands with 1521 species and Canary Islands with 2066 species. Extinct species are included in the analysis, with an extinction rate of 0.35% of the flora. A total of 1488 endemic species are recognized, which account for 21% of the Spanish flora. The rate of endemism in the Canary Islands is 25.9%, considerably higher than for the Balearic Islands (6.9%) and for mainland Spain (13.8%). A list of the 35 strict endemic genera is compiled, of which 65.7% are Canarian, and another list of 27 subendemic genera of which 48.1% are also Canarian. An estimated 12% of the Spanish flora is non-native, with large variation between the 20.7% of the Canary flora, 10.5% of mainland Spain and 9.7% of the Balearic Islands. Finally, the composition of the Spanish flora for large groups and families is ana lysed. The data show that species richness and endemicity rates have been overestimated by previous authors, and are similar to other Mediterranean countries. It is concluded that a complete revision of the Macaronesian flora is strongly needed to obtain an accurate comparison with the flora of other areas.</p></div>
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Data from an updated and revised checklist of the Spanish flora is analyzed. The Spanish vascular plant flora is composed of 204 families, 1433 genera and 7071 species. Floristic data are analysed by considering three regions: mainland Spain with 5984 species, the Balearic Islands with 1521 species and Canary Islands with 2066 species. Extinct species are included in the analysis, with an extinction rate of 0.35% of the flora. A total of 1488 endemic species are recognized, which account for 21% of the Spanish flora. The rate of endemism in the Canary Islands is 25.9%, considerably higher than for the Balearic Islands (6.9%) and for mainland Spain (13.8%). A list of the 35 strict endemic genera is compiled, of which 65.7% are Canarian, and another list of 27 subendemic genera of which 48.1% are also Canarian. An estimated 12% of the Spanish flora is non-native, with large variation between the 20.7% of the Canary flora, 10.5% of mainland Spain and 9.7% of the Balearic Islands. Finally, the composition of the Spanish flora for large groups and families is ana lysed. The data show that species richness and endemicity rates have been overestimated by previous authors, and are similar to other Mediterranean countries. It is concluded that a complete revision of the Macaronesian flora is strongly needed to obtain an accurate comparison with the flora of other areas.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00045.x" xmlns="http://purl.org/rss/1.0/"><title> Cardamine calliphaea sp. nov. (Brassicaceae) from southwestern Greece</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00045.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Cardamine calliphaea sp. nov. (Brassicaceae) from southwestern Greece</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kit Tan, Konstantinos Giannopoulos, Gert Vold</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-10T05:26:49.905077-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.00045.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.1756-1051.2012.00045.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00045.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Cardamine calliphaea</em> Kit Tan, G. Vold &amp; Giannopoulos sp. nov. (Brassicaceae) is illustrated and described as a new species endemic to Greece. It occurs in the prefectures of Ilia in western Peloponnese and Etolias-Akarnanias in western Sterea Ellas and bears some resemblance to <em>C. graeca</em>, differing by its dense greyish–white indumentum and by the absence of leaf auricles. Affinities lie with <em>C. glauca</em> and <em>C. plumieri</em> from which it differs conspicuously, among other characters, by its imparipinnate leaves with the terminal leaflet smaller or equal in size to the lateral pairs.</p></div>
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Cardamine calliphaea Kit Tan, G. Vold &amp; Giannopoulos sp. nov. (Brassicaceae) is illustrated and described as a new species endemic to Greece. It occurs in the prefectures of Ilia in western Peloponnese and Etolias-Akarnanias in western Sterea Ellas and bears some resemblance to C. graeca, differing by its dense greyish–white indumentum and by the absence of leaf auricles. Affinities lie with C. glauca and C. plumieri from which it differs conspicuously, among other characters, by its imparipinnate leaves with the terminal leaflet smaller or equal in size to the lateral pairs.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00003.x" xmlns="http://purl.org/rss/1.0/"><title> Yuchengia, a new polypore genus segregated from Perenniporia (Polyporales) based on morphological and molecular evidence</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00003.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Yuchengia, a new polypore genus segregated from Perenniporia (Polyporales) based on morphological and molecular evidence</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Chang-Lin Zhao, Bao-Kai Cui, Kari Timo Steffen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-10T05:25:28.874929-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.00003.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.1756-1051.2012.00003.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00003.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Yuchengia</em> gen. nov. is proposed to accommodate <em>Perenniporia narymica</em>. It represents a monophyletic lineage within the core polyporoid clade based on sequences of the rDNA ITS and nLSU regions, and it is distinct from <em>Perenniporia</em> s.s. <em>Yuchengia</em> shares some characters with <em>Perenniporia</em>, both having thick-walled and cyanophilous basidiospores, but differs by having acyanophilous and amyloid skeletal hyphae dissolving in KOH, and non-dextrinoid basidiospores.</p></div>
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Yuchengia gen. nov. is proposed to accommodate Perenniporia narymica. It represents a monophyletic lineage within the core polyporoid clade based on sequences of the rDNA ITS and nLSU regions, and it is distinct from Perenniporia s.s. Yuchengia shares some characters with Perenniporia, both having thick-walled and cyanophilous basidiospores, but differs by having acyanophilous and amyloid skeletal hyphae dissolving in KOH, and non-dextrinoid basidiospores.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01445.x" xmlns="http://purl.org/rss/1.0/"><title>Comparative microsporogenesis and anther development of selected species from Magnoliaceae</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01445.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparative microsporogenesis and anther development of selected species from Magnoliaceae</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Feng-Xia Xu, Dong-Qin Chen, Chelsea Specht</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-09T04:28:29.862059-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01445.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.1756-1051.2012.01445.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01445.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Stamen development and microsporogenesis of four species from Magnoliaceae was investigated in order to provide additional data from this family. Stamen bases were found to be wide and short, without morphological differentiation in <em>Magnolia moto, M. paenetalauma</em> and <em>Woonyoungia septentrionalis</em>. In contrast, stamens are distinctly differentiated into anther and filament regions in <em>Michelia crassipes.</em> The orientation of dehiscence is introrse, introrse-latrorse and latrorse in <em>M. moto, M. paenetalauma</em> and <em>M. crassipes</em>, respectively. The vascular bundles range from three to five (<em>M. moto, M. paenetalauma</em>) to one (<em>M. crassipes</em>). The amount of the connective tissue has been reduced from three to two times of the sporogenous tissue in <em>M. moto</em> and <em>M. paenetalauma</em>. The two parts are nearly equal in <em>M. crassipess</em>. In <em>W. septentrionalis</em>, the orientation of dehiscence, the vascular bundles and the size of the connective tissue vary in different parts of the floral receptacle. The endothecium and endothecial-like cells form a ring that encloses the entire anther. The middle layer cells originate from both the outer and inner secondary parietal layers, and start to degenerate gradually at the microspore interphase stage or meiosis stage. The tapetum is of the secretory type, derived from the inner secondary parietal cells. The mature anther wall is composed of one epidermal, one endothecial, three to four middle layer(s) and one glandular tapetum. Only one epidermis, one endothecium, and the remnants of the middle layer and tapetum are left before anther dehiscence. Microspore tetrads appear as isobilateral, tetrahedral, decussate and T-shaped, produced by a modified simultaneous microsporogenesis, which have evolved from the common ancestor of all Magnoliaceae. Our results support an ancestral state with stamens with non-marginal sporangia and the amount of sterile tissue exceeding the amount of sporogenous tissue, and evolutionary trends toward equalization of the amount of fertile and sterile tissue on the stamen.</p></div>
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Stamen development and microsporogenesis of four species from Magnoliaceae was investigated in order to provide additional data from this family. Stamen bases were found to be wide and short, without morphological differentiation in Magnolia moto, M. paenetalauma and Woonyoungia septentrionalis. In contrast, stamens are distinctly differentiated into anther and filament regions in Michelia crassipes. The orientation of dehiscence is introrse, introrse-latrorse and latrorse in M. moto, M. paenetalauma and M. crassipes, respectively. The vascular bundles range from three to five (M. moto, M. paenetalauma) to one (M. crassipes). The amount of the connective tissue has been reduced from three to two times of the sporogenous tissue in M. moto and M. paenetalauma. The two parts are nearly equal in M. crassipess. In W. septentrionalis, the orientation of dehiscence, the vascular bundles and the size of the connective tissue vary in different parts of the floral receptacle. The endothecium and endothecial-like cells form a ring that encloses the entire anther. The middle layer cells originate from both the outer and inner secondary parietal layers, and start to degenerate gradually at the microspore interphase stage or meiosis stage. The tapetum is of the secretory type, derived from the inner secondary parietal cells. The mature anther wall is composed of one epidermal, one endothecial, three to four middle layer(s) and one glandular tapetum. Only one epidermis, one endothecium, and the remnants of the middle layer and tapetum are left before anther dehiscence. Microspore tetrads appear as isobilateral, tetrahedral, decussate and T-shaped, produced by a modified simultaneous microsporogenesis, which have evolved from the common ancestor of all Magnoliaceae. Our results support an ancestral state with stamens with non-marginal sporangia and the amount of sterile tissue exceeding the amount of sporogenous tissue, and evolutionary trends toward equalization of the amount of fertile and sterile tissue on the stamen.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01566.x" xmlns="http://purl.org/rss/1.0/"><title> Campanula mugeana sp. nov. (Campanulaceae) from western Anatolia, Turkey</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01566.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Campanula mugeana sp. nov. (Campanulaceae) from western Anatolia, Turkey</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hasan Yıldırım</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-07T09:21:37.970864-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01566.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.1756-1051.2012.01566.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01566.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Campanula mugeana</em> Yıldırım (Campanulaceae) is described as a new species. Diagnostic morphological characters, full descriptions and detailed illustrations of the new species are given. Micrographs of seeds and pollen were taken with scanning electron microscopy (SEM). <em>Campanula mugeana</em> is restricted to the province of İzmir in western Anatolia, Turkey. It belongs to the section <em>Quinqueloculares</em>, subgenus <em>Campanula</em> based on floral features. Although <em>C. mugeana</em> has no close relatives within sect. <em>Quinqueloculares</em>, it shows some morphological similarities with <em>C. saxatilis</em> and <em>C. davisii.</em></p></div>
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Campanula mugeana Yıldırım (Campanulaceae) is described as a new species. Diagnostic morphological characters, full descriptions and detailed illustrations of the new species are given. Micrographs of seeds and pollen were taken with scanning electron microscopy (SEM). Campanula mugeana is restricted to the province of İzmir in western Anatolia, Turkey. It belongs to the section Quinqueloculares, subgenus Campanula based on floral features. Although C. mugeana has no close relatives within sect. Quinqueloculares, it shows some morphological similarities with C. saxatilis and C. davisii.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01706.x" xmlns="http://purl.org/rss/1.0/"><title>Mating system variation in Veronica (Plantaginaceae): inferences from pollen/ovule ratios and other reproductive traits</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01706.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Mating system variation in Veronica (Plantaginaceae): inferences from pollen/ovule ratios and other reproductive traits</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Romain Scalone, Markus Kolf, Dirk C. Albach</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T09:19:10.634372-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01706.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.1756-1051.2012.01706.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01706.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>The pollen–ovule ratio (P/O) is commonly used to estimate the mode of sexual reproduction in flowering plants. In previous studies, a clear correspondence has been detected between this character and the degree of autogamy. We here investigate variation in this character and its expected correlates in the genus <em>Veronica</em> (Plantaginaceae). Pollen–ovule ratios of 45 species representing eleven percent of all the species in the genus were investigated and compared with results from crossing experiments from previous studies. In addition, multiple populations of 17 of the 45 studied species were sampled and a controlled-environment experiment was conducted to evaluate the extent of intraspecific variation. Moreover, relationships between P/O and other primary and secondary reproductive characters of the <em>Veronica</em> flower were investigated in relation to a phylogenetic hypothesis in order to determine the phylogenetic constraints on reproductive characters. The differences in P/O among species correspond well to the diversity of mating systems in <em>Veronica</em> and correlate well with other floral characters such as corolla size. These characters together seem to allow a powerful and fast tool to infer mating systems. However, causes for intraspecific variation of P/O, such as different cytotypes, ecotypes or different growth conditions, need to be considered.</p></div>
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The pollen–ovule ratio (P/O) is commonly used to estimate the mode of sexual reproduction in flowering plants. In previous studies, a clear correspondence has been detected between this character and the degree of autogamy. We here investigate variation in this character and its expected correlates in the genus Veronica (Plantaginaceae). Pollen–ovule ratios of 45 species representing eleven percent of all the species in the genus were investigated and compared with results from crossing experiments from previous studies. In addition, multiple populations of 17 of the 45 studied species were sampled and a controlled-environment experiment was conducted to evaluate the extent of intraspecific variation. Moreover, relationships between P/O and other primary and secondary reproductive characters of the Veronica flower were investigated in relation to a phylogenetic hypothesis in order to determine the phylogenetic constraints on reproductive characters. The differences in P/O among species correspond well to the diversity of mating systems in Veronica and correlate well with other floral characters such as corolla size. These characters together seem to allow a powerful and fast tool to infer mating systems. However, causes for intraspecific variation of P/O, such as different cytotypes, ecotypes or different growth conditions, need to be considered.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01532.x" xmlns="http://purl.org/rss/1.0/"><title>Trichome micromorphology in Turkish species of Ziziphora (Lamiaceae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01532.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Trichome micromorphology in Turkish species of Ziziphora (Lamiaceae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ayla Kaya, Fatih Satil, Tuncay Dirmenci, Selami Selvi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-06T10:43:01.069474-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01532.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.1756-1051.2012.01532.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01532.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Ziziphora</em> L. is represented by 5 species and 2 subspecies in the flora of Turkey: <em>Z. clinopodioides, Z. capitata, Z. persica, Z. tenuior, Z. taurica</em> subsp. <em>taurica, Z. taurica</em> subsp. <em>cleonioides.</em> It is difficult to distinguish between some <em>Ziziphora</em> taxa because of their morphological similarities. In this study, the leaf and calyx trichomes of <em>Ziziphora</em> taxa in Turkey were studied in order to assess anatomical variations that may serve as distinguishing characters. Their micromorphological features were surveyed by scanning electron microscopy (SEM) and light microscopy (LM). Trichomes on leaves and calyx can be divided into two general types: non-glandular trichomes and glandular (secretory) trichomes. The non- glandular trichomes are simple, acicular or curved with cuticular micropapillae. They usually consist of one or more additional cells. The glandular trichomes are divided into two types: peltate and capitate and <em>Ziziphora</em> taxa can easily be distinguished by presence/absence, density and types of glandular trichomes on leaves and calyx. The peltate trichomes consist of 12 or 18 secretory head cells in a single disc; four or six central cells surrounded by eight or twelve peripheral ones. Peltate trichomes are absent on the adaxial leaf surface of <em>Z. capitata</em> and <em>Z. persica.</em> Two types of capitate trichomes are present in <em>Ziziphora</em>. The capitate trichomes are only absent on the calyx surface of <em>Z. persica.</em> In addition, the trichome micromorphology provides some support for separating the two subspecies of <em>Z. taurica</em>. In conclusion, <em>Ziziphora</em> taxa can easily be distinguished by cell number, cell shape presence/absence and density of the glandular trichomes on leaves and calyx.</p></div>
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Ziziphora L. is represented by 5 species and 2 subspecies in the flora of Turkey: Z. clinopodioides, Z. capitata, Z. persica, Z. tenuior, Z. taurica subsp. taurica, Z. taurica subsp. cleonioides. It is difficult to distinguish between some Ziziphora taxa because of their morphological similarities. In this study, the leaf and calyx trichomes of Ziziphora taxa in Turkey were studied in order to assess anatomical variations that may serve as distinguishing characters. Their micromorphological features were surveyed by scanning electron microscopy (SEM) and light microscopy (LM). Trichomes on leaves and calyx can be divided into two general types: non-glandular trichomes and glandular (secretory) trichomes. The non- glandular trichomes are simple, acicular or curved with cuticular micropapillae. They usually consist of one or more additional cells. The glandular trichomes are divided into two types: peltate and capitate and Ziziphora taxa can easily be distinguished by presence/absence, density and types of glandular trichomes on leaves and calyx. The peltate trichomes consist of 12 or 18 secretory head cells in a single disc; four or six central cells surrounded by eight or twelve peripheral ones. Peltate trichomes are absent on the adaxial leaf surface of Z. capitata and Z. persica. Two types of capitate trichomes are present in Ziziphora. The capitate trichomes are only absent on the calyx surface of Z. persica. In addition, the trichome micromorphology provides some support for separating the two subspecies of Z. taurica. In conclusion, Ziziphora taxa can easily be distinguished by cell number, cell shape presence/absence and density of the glandular trichomes on leaves and calyx.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01541.x" xmlns="http://purl.org/rss/1.0/"><title>The identity of the genus Metaeritrichium in Boraginaceae</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01541.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The identity of the genus Metaeritrichium in Boraginaceae</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bao-Cai Han, Ming-Li Zhang, David J. Goyder</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-03T10:55:33.60911-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01541.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.1756-1051.2012.01541.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01541.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Metaeritrichium</em> has been considered monotypic and endemic to China in traditional taxonomic treatments. However, our examinations of specimens and bibliography, combined with field observations, reveal that <em>Metaeritrichium microuloides</em> is conspecific with <em>Actinocarya acaulis. Metaeritrichium</em> is therefore treated as a synonym of <em>Actinocarya</em>. We also clarify the typification of <em>Actinocarya acaulis.</em></p></div>]]></content:encoded><description>Metaeritrichium has been considered monotypic and endemic to China in traditional taxonomic treatments. However, our examinations of specimens and bibliography, combined with field observations, reveal that Metaeritrichium microuloides is conspecific with Actinocarya acaulis. Metaeritrichium is therefore treated as a synonym of Actinocarya. We also clarify the typification of Actinocarya acaulis.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2013.00082.x" xmlns="http://purl.org/rss/1.0/"><title>Topography as a driver of local terrestrial vascular plant diversity patterns</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2013.00082.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Topography as a driver of local terrestrial vascular plant diversity patterns</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jesper Erenskjold Moeslund, Lars Arge, Peder Klith Bøcher, Tommy Dalgaard, Jens-Christian Svenning</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T09:09:15.49954-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2013.00082.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.1756-1051.2013.00082.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2013.00082.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">129</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">144</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>At landscape and regional scales topography is recognized as one of the most important determinants of vascular plant diversity, primarily due to the influence of mountains. As temperature changes markedly over the elevation ranges in mountain areas, topography offers a wide variety of different habitats as well as buffering against climate change. However, for local vegetation, notably in lowland areas, the general importance of topography is less well recognized and the mechanisms by which it exerts influence on local vascular plant diversity are not comprehensively understood. In this review, we provide an overview of the evidence for the different mechanisms involved in topography’s control of local patterns in potential vegetation drivers, namely incident solar energy, wind exposure, hydrology, geochemistry, and biotic conditions. Furthermore, we review the processes through which these factors shape local terrestrial vascular plant diversity patterns and provide directions for future studies on this topic. We find that topography is an important factor for local vascular plant diversity patterns in a broad range of habitats throughout the world, even in relatively flat lowlands. However, the mechanisms involved are varied and complex. Local patterns in soil moisture seem to be affected by topography through more mechanisms than other topographically controlled factors and have a strong and consistent influence on local plant diversity. Hence, local hydrology is probably the main mechanistic factor through which topography influences local terrestrial vascular plant diversity patterns. Future research should focus on employing high-coverage fine-resolution topographic data to comprehensively explore the role of topography in controlling local dynamics over large areas. Moreover, we recommend including several different habitats, particularly those in which the role of topography is poorly understood. Finally, we propose to integrate relevant functional topographic variables such as topographic wetness indices instead of simple topographic measures into future investigations.</p></div>
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At landscape and regional scales topography is recognized as one of the most important determinants of vascular plant diversity, primarily due to the influence of mountains. As temperature changes markedly over the elevation ranges in mountain areas, topography offers a wide variety of different habitats as well as buffering against climate change. However, for local vegetation, notably in lowland areas, the general importance of topography is less well recognized and the mechanisms by which it exerts influence on local vascular plant diversity are not comprehensively understood. In this review, we provide an overview of the evidence for the different mechanisms involved in topography’s control of local patterns in potential vegetation drivers, namely incident solar energy, wind exposure, hydrology, geochemistry, and biotic conditions. Furthermore, we review the processes through which these factors shape local terrestrial vascular plant diversity patterns and provide directions for future studies on this topic. We find that topography is an important factor for local vascular plant diversity patterns in a broad range of habitats throughout the world, even in relatively flat lowlands. However, the mechanisms involved are varied and complex. Local patterns in soil moisture seem to be affected by topography through more mechanisms than other topographically controlled factors and have a strong and consistent influence on local plant diversity. Hence, local hydrology is probably the main mechanistic factor through which topography influences local terrestrial vascular plant diversity patterns. Future research should focus on employing high-coverage fine-resolution topographic data to comprehensively explore the role of topography in controlling local dynamics over large areas. Moreover, we recommend including several different habitats, particularly those in which the role of topography is poorly understood. Finally, we propose to integrate relevant functional topographic variables such as topographic wetness indices instead of simple topographic measures into future investigations.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01558.x" xmlns="http://purl.org/rss/1.0/"><title>The role of the Weberian Reform in European Rubus research and the taxonomy of locally distributed species – which species should we describe?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01558.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The role of the Weberian Reform in European Rubus research and the taxonomy of locally distributed species – which species should we describe?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rense Haveman, Iris de Ronde</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-04-27T10:19:29.693326-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01558.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.1756-1051.2012.01558.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01558.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">145</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">150</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>After Sudre published his treatment of European <em>Rubi</em> in the early 20th century, <em>Rubus</em> taxonomy in Europe suffered from a scholastic phase and a longer period of stagnation. The so-called ‘Weberian Reform’ initiated the necessary revival of European batology. It rests on four major pillars: 1) mapping projects over larger areas, 2) evaluation of type material, 3) visits to loci classici, and 4) evaluation of the status of species by means of their distribution areas. Subsequently, it has become widely accepted in European batology that only species with a distribution area over 50 km should be described. Although this pragmatic species concept has been useful in making a continent-wide overview of brambles, we argue that it is lacking a scientific basis, and should thus be rejected.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>There are at least four distinctive problems when treating locally distributed brambles: 1) primary hybrids, 2) locally distributed stabilised apomicts, 3) intraspecific variation in species with a larger distribution range, and 4) unstabilised swarms of hybridogenic biotypes and the derivates thereof (mainly in the montane regions). When facing the problems in <em>Rubus</em> systematics, we argue that all independently evolving lineages should be described as species, including apomictic lineages with very small distribution ranges, both from the mountain-dwelling glandular series and from the lowlands. Neither primary hybrids (which are not stabilised by apomixis), nor biotypes without an independent and coherent distribution area are independently evolving lineages, and should thus not be described as species. We advocate a restrained attitude when describing new species with limited distribution areas.</p></div>
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After Sudre published his treatment of European Rubi in the early 20th century, Rubus taxonomy in Europe suffered from a scholastic phase and a longer period of stagnation. The so-called ‘Weberian Reform’ initiated the necessary revival of European batology. It rests on four major pillars: 1) mapping projects over larger areas, 2) evaluation of type material, 3) visits to loci classici, and 4) evaluation of the status of species by means of their distribution areas. Subsequently, it has become widely accepted in European batology that only species with a distribution area over 50 km should be described. Although this pragmatic species concept has been useful in making a continent-wide overview of brambles, we argue that it is lacking a scientific basis, and should thus be rejected.
There are at least four distinctive problems when treating locally distributed brambles: 1) primary hybrids, 2) locally distributed stabilised apomicts, 3) intraspecific variation in species with a larger distribution range, and 4) unstabilised swarms of hybridogenic biotypes and the derivates thereof (mainly in the montane regions). When facing the problems in Rubus systematics, we argue that all independently evolving lineages should be described as species, including apomictic lineages with very small distribution ranges, both from the mountain-dwelling glandular series and from the lowlands. Neither primary hybrids (which are not stabilised by apomixis), nor biotypes without an independent and coherent distribution area are independently evolving lineages, and should thus not be described as species. We advocate a restrained attitude when describing new species with limited distribution areas.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00012.x" xmlns="http://purl.org/rss/1.0/"><title>Identification and typification of Nepenthes blancoi, with N. abalata sp. nov. from the western Visayas, Philippines</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00012.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Identification and typification of Nepenthes blancoi, with N. abalata sp. nov. from the western Visayas, Philippines</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Martin Cheek, Matthew Jebb</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T05:30:30.81739-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.00012.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.1756-1051.2012.00012.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.00012.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">151</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">156</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Nepenthes blancoi</em> Bl. is neotypified on material conspecific with <em>N. alata</em> Blanco. Material previously associated with <em>N. blancoi</em> is described as <em>N. abalata</em> Jebb &amp; Cheek sp. nov. This is a grassland species seemingly related to <em>N. philippinensis</em> Macfarl. but with similarities to the grassland species of Indo-China. Its conservation status is assessed as ‘Critically Endangered’ (CR).</p></div>
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Nepenthes blancoi Bl. is neotypified on material conspecific with N. alata Blanco. Material previously associated with N. blancoi is described as N. abalata Jebb &amp; Cheek sp. nov. This is a grassland species seemingly related to N. philippinensis Macfarl. but with similarities to the grassland species of Indo-China. Its conservation status is assessed as ‘Critically Endangered’ (CR).
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01150.x" xmlns="http://purl.org/rss/1.0/"><title> Maclurochloa tonkinensis sp. nov. (Poaceae: Bambusoideae) from Vietnam</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01150.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Maclurochloa tonkinensis sp. nov. (Poaceae: Bambusoideae) from Vietnam</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hoang Nghia Nguyen, Van Tien Tran</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T09:09:15.49954-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01150.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.1756-1051.2012.01150.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01150.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">157</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">160</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Maclurochloa</em> K. M. Wong (Gramineae: Bambusoideae) is a genus of clambering bamboos with dry caryopses. It was thought to be monotypic in Peninsular Malaysia, but here we report one more species from Vietnam which is new to science: <em>Maclurochloa tonkinensis</em> H. N. Nguyen et V. T. Tran sp. nov. <em>Maclurochloa tonkinensis</em> is most similar to <em>M. montana</em> (Ridl.) K. M. Wong from which differs mainly by having internodes 50–58 × 3.0–3.5 cm and culm leaves with auriculate sheaths and erect blade.</p></div>
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Maclurochloa K. M. Wong (Gramineae: Bambusoideae) is a genus of clambering bamboos with dry caryopses. It was thought to be monotypic in Peninsular Malaysia, but here we report one more species from Vietnam which is new to science: Maclurochloa tonkinensis H. N. Nguyen et V. T. Tran sp. nov. Maclurochloa tonkinensis is most similar to M. montana (Ridl.) K. M. Wong from which differs mainly by having internodes 50–58 × 3.0–3.5 cm and culm leaves with auriculate sheaths and erect blade.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01207.x" xmlns="http://purl.org/rss/1.0/"><title> Nanooravia gen. nov., subtribe Dimeriinae (Poaceae–Panicoideae–Andropogoneae) from India</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01207.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Nanooravia gen. nov., subtribe Dimeriinae (Poaceae–Panicoideae–Andropogoneae) from India</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. S. Kiran Raj, M. Sivadasan, J. F. Veldkamp, A. H. Alfarhan, Jacob Thomas</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T09:09:15.49954-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01207.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.1756-1051.2012.01207.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01207.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">161</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">165</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>The new genus <em>Nanooravia</em> Kiran Raj &amp; Sivad. (Poaceae–Andropogoneae–Dimeriinae) from the southwestern Ghats in India is described and illustrated, and the new combination <em>N. santapaui</em> (M. R. Almeida) Kiran Raj &amp; Sivad. is made. The genus is characterized by its usually unequal and intertwined racemes, triquetrous rachis, extremely oblique and glabrous pedicel tip, distantly arranged spikelets, long trigonous callus with oblique tip and densely covered with golden–yellow or yellowish–brown hairs along one angle, keel-less glumes with a dorsally echinate apex and apically auricled margins, and an upper lemma with a stout awn having a long column. The new genus is distinct from <em>Dimeria</em> R. Br. in which the species was originally described, but is similar to the monotypic Indian genus <em>Pogonachne</em> Bor currently placed in the subtribe Ischaeminae. It occurs in Peninsular India, a region considered as the centre of diversity of the subtribe with more than 50% of the known <em>Dimeria</em> species, including numerous endemics.</p></div>
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The new genus Nanooravia Kiran Raj &amp; Sivad. (Poaceae–Andropogoneae–Dimeriinae) from the southwestern Ghats in India is described and illustrated, and the new combination N. santapaui (M. R. Almeida) Kiran Raj &amp; Sivad. is made. The genus is characterized by its usually unequal and intertwined racemes, triquetrous rachis, extremely oblique and glabrous pedicel tip, distantly arranged spikelets, long trigonous callus with oblique tip and densely covered with golden–yellow or yellowish–brown hairs along one angle, keel-less glumes with a dorsally echinate apex and apically auricled margins, and an upper lemma with a stout awn having a long column. The new genus is distinct from Dimeria R. Br. in which the species was originally described, but is similar to the monotypic Indian genus Pogonachne Bor currently placed in the subtribe Ischaeminae. It occurs in Peninsular India, a region considered as the centre of diversity of the subtribe with more than 50% of the known Dimeria species, including numerous endemics.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01557.x" xmlns="http://purl.org/rss/1.0/"><title> Ceropegia pullaiahii sp. nov. (Apocynaceae, Asclepiadoideae) from India</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01557.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Ceropegia pullaiahii sp. nov. (Apocynaceae, Asclepiadoideae) from India</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. R. Kullayiswamy, S. Sandhyarani, S. Karuppusamy</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-07T10:34:17.594728-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01557.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.1756-1051.2012.01557.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01557.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">166</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">169</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Ceropegia pullaiahii</em> Kullayiswamy, Sandhyarani et Karuppusamy sp. nov. (Apocynaceae) is described from open dry deciduous forest of Anantapur district, Andhra Pradesh, India. Its tubers are eaten by the local people. It is similar to <em>C. mahabalei</em> Hemadri et Ansari but differs in its twining habit and 3-flowered cyme.</p></div>
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Ceropegia pullaiahii Kullayiswamy, Sandhyarani et Karuppusamy sp. nov. (Apocynaceae) is described from open dry deciduous forest of Anantapur district, Andhra Pradesh, India. Its tubers are eaten by the local people. It is similar to C. mahabalei Hemadri et Ansari but differs in its twining habit and 3-flowered cyme.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01624.x" xmlns="http://purl.org/rss/1.0/"><title> Abelmoschus enbeepeegearense sp. nov. (Malvaceae), an endemic species of okra from Western Ghats, India</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01624.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Abelmoschus enbeepeegearense sp. nov. (Malvaceae), an endemic species of okra from Western Ghats, India</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Joseph John, Sheen Scariah, V. A. Muhammed Nissar, K. V. Bhat, S. R. Yadav</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-25T05:32:26.227018-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01624.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.1756-1051.2012.01624.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01624.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">170</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">175</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Abelmoschus enbeepeegearense</em> J. John et al. is a new species occurring at low elevations in the Western Ghats of India, comprising Kerala, Karnataka and Tamil Nadu. The taxon is morphologically allied to <em>A. moschatus</em> subsp. <em>moschatus, A. moschatus</em> subsp. <em>tuberosus</em> and <em>A. crinitus</em>, but easily distinguishable by virtue of its orthotropic branching, 3–5-angled leaves, glandular hairy plant body with whitish waxy secretions, glandular non-setose epiclayx segmens which is more than eight in number and ovate hirsute fruits with a short mucro at the apex. It can be crossed with all three taxa with varying degree of success, but the hybrids are sterile. The material belonging to it was earlier identified as and placed under <em>A. moschatus</em> Medik. The taxon is described and illustrated with notes on its phenology, ecology and distribution. In additions, a key to all <em>Abelmoschus</em> taxa occurring in India is provided.</p></div>
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Abelmoschus enbeepeegearense J. John et al. is a new species occurring at low elevations in the Western Ghats of India, comprising Kerala, Karnataka and Tamil Nadu. The taxon is morphologically allied to A. moschatus subsp. moschatus, A. moschatus subsp. tuberosus and A. crinitus, but easily distinguishable by virtue of its orthotropic branching, 3–5-angled leaves, glandular hairy plant body with whitish waxy secretions, glandular non-setose epiclayx segmens which is more than eight in number and ovate hirsute fruits with a short mucro at the apex. It can be crossed with all three taxa with varying degree of success, but the hybrids are sterile. The material belonging to it was earlier identified as and placed under A. moschatus Medik. The taxon is described and illustrated with notes on its phenology, ecology and distribution. In additions, a key to all Abelmoschus taxa occurring in India is provided.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01609.x" xmlns="http://purl.org/rss/1.0/"><title>Four new species of Adenocalymma (Bignoniaceae) and a key to the species from southeastern Brazil</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01609.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Four new species of Adenocalymma (Bignoniaceae) and a key to the species from southeastern Brazil</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Renata Giassi Udulutsch, Marco Antonio de Assis, Pedro Dias</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-11T09:26:13.868683-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01609.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.1756-1051.2012.01609.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01609.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">176</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">185</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Four new species of <em>Adenocalymma</em> (Bignoniaceae, Bignonieae) from southeastern Brazil are described and illustrated: <em>A. aurantiacum</em>, characterized by dark orange and infundibuliform corolla; <em>A. cinereum</em>, characterized by shrubby habit, greyish inflorescence, infundibuliform corolla, and exserted stamens; <em>A. gibbosum</em>, characterized by gibbous and orange corolla and an inflorescence with dendritic trichomes; and <em>A. sessile</em>, characterized by sessile leaves and gibbous corolla. A discussion on the relationships of the new taxa and a key to all 29 species of <em>Adenocalymma</em> reported from southeastern Brazil are provided.</p></div>
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Four new species of Adenocalymma (Bignoniaceae, Bignonieae) from southeastern Brazil are described and illustrated: A. aurantiacum, characterized by dark orange and infundibuliform corolla; A. cinereum, characterized by shrubby habit, greyish inflorescence, infundibuliform corolla, and exserted stamens; A. gibbosum, characterized by gibbous and orange corolla and an inflorescence with dendritic trichomes; and A. sessile, characterized by sessile leaves and gibbous corolla. A discussion on the relationships of the new taxa and a key to all 29 species of Adenocalymma reported from southeastern Brazil are provided.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01186.x" xmlns="http://purl.org/rss/1.0/"><title>Reinstatement of the name Lithocarpus longinux (Fagaceae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01186.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reinstatement of the name Lithocarpus longinux (Fagaceae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wei Zhou, Yu-Song Huang, Nian-He Xia</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T09:09:15.49954-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01186.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.1756-1051.2012.01186.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01186.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">186</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">189</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>The name <em>Lithocarpus longinux</em> (Hu) Chun ex Y. C. Hsu &amp; H. W. Jen is reinstated. It used to be treated as a synonym of <em>L. areca</em> (Hickel &amp; A. Camus) A. Camus, but morphological characters of cupules and leaves support the reinstatement. These two species, together with <em>L. longzhouicus</em> (C. C. Huang &amp; Y. T. Chang) J. Q. Li &amp; L. Chen, make up a small group that is distributed in limestone areas and have similar morphological characters. A key is provided to distinguish between them, and their is discussed.</p></div>
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The name Lithocarpus longinux (Hu) Chun ex Y. C. Hsu &amp; H. W. Jen is reinstated. It used to be treated as a synonym of L. areca (Hickel &amp; A. Camus) A. Camus, but morphological characters of cupules and leaves support the reinstatement. These two species, together with L. longzhouicus (C. C. Huang &amp; Y. T. Chang) J. Q. Li &amp; L. Chen, make up a small group that is distributed in limestone areas and have similar morphological characters. A key is provided to distinguish between them, and their is discussed.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01540.x" xmlns="http://purl.org/rss/1.0/"><title> Juncus fernandez-carvajaliae sp. nov. (Juncaceae) from Castilla-La Mancha, central Spain</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01540.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Juncus fernandez-carvajaliae sp. nov. (Juncaceae) from Castilla-La Mancha, central Spain</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Romero-Zarco, V. J. Arán</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T09:09:15.49954-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01540.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.1756-1051.2012.01540.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01540.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">190</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">193</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Juncus fernandez-carvajaliae</em> Romero Zarco &amp; Arán sp. nov. (Juncaceae), collected from Castilla-La Mancha in central Spain, is described and illustrated. The main distinguishing features of the new species are compared with allied species of <em>J.</em> sect.<em>Tenageia</em>.</p></div>
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Juncus fernandez-carvajaliae Romero Zarco &amp; Arán sp. nov. (Juncaceae), collected from Castilla-La Mancha in central Spain, is described and illustrated. The main distinguishing features of the new species are compared with allied species of J. sect.Tenageia.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01396.x" xmlns="http://purl.org/rss/1.0/"><title> Limonium cedrorum sp. nov. (Plumbaginaceae) from Lebanon</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01396.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Limonium cedrorum sp. nov. (Plumbaginaceae) from Lebanon</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gianniantonio Domina, Francesco M. Raimondo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-17T04:59:36.749016-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01396.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.1756-1051.2012.01396.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01396.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">194</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">197</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Limonium cedrorum</em> Domina &amp; Ramondo, a new species belonging to the <em>L. palmare</em> aggr., is described and illustrated from the inland near Becharre (Lebanon). Its relationships with morphologically close taxa are discussed. <em>Limonium cedrorum</em> differs from <em>L. sieberi</em> and <em>L. postii</em> mainly by looser inflorescences and larger flowers. It differs from <em>L. galilaeum</em> by longer outer bract and longer scale below the first inflorescence branch, few sterile branches, thicker base of the inflorescence and denser spikes, and from <em>L. graecum</em> by the shape of the inflorescence, longer basal internodes and the shape of the calyx.</p></div>
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Limonium cedrorum Domina &amp; Ramondo, a new species belonging to the L. palmare aggr., is described and illustrated from the inland near Becharre (Lebanon). Its relationships with morphologically close taxa are discussed. Limonium cedrorum differs from L. sieberi and L. postii mainly by looser inflorescences and larger flowers. It differs from L. galilaeum by longer outer bract and longer scale below the first inflorescence branch, few sterile branches, thicker base of the inflorescence and denser spikes, and from L. graecum by the shape of the inflorescence, longer basal internodes and the shape of the calyx.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01452.x" xmlns="http://purl.org/rss/1.0/"><title>Taxonomic status of the subspecies of Teucrium lamiifolium in Turkey: reevaluation based on macro- and micro-morphology, anatomy and chemistry</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01452.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Taxonomic status of the subspecies of Teucrium lamiifolium in Turkey: reevaluation based on macro- and micro-morphology, anatomy and chemistry</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Süleyman Doğu, Muhittin Dinç, Ayla Kaya, Betül Demirci</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-06T07:35:26.035083-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01452.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.1756-1051.2012.01452.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01452.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">198</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">207</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Teucrium stachyophyllum</em> P. H. Davis was first described as a separate species in the ‘Syrian, Lebanon and Palestine Flora’, but was reduced to a subspecies of <em>T. lamiifolium</em> d’Urv. in the ‘Turkish Flora’. Studies on the macro- and micro-morphology as well as the anatomy of populations of <em>T. lamiifolium</em> subsp. <em>stachyophyllum</em> (P. H. Davis) Hedge &amp; Ekim and <em>T. lamiifolium</em> subsp. <em>lamiifolium</em> in Turkey have been carried out based on herbarium specimens and field observations. The results from the anatomical studies on stems and leaves show that although the two taxa are similar in stem anatomy, they differ in terms of mesophyll thickness and occurrence of crystals in the upper epidermal cells of the leaf. Light and scanning electron microscope analyzes revealed striking differences in colour, size, sculpture and gland density between nutlets of the two taxa. Morphological studies also showed that there were important differences between the two taxa in terms of inflorescence, indumentum, and stem length and thickness. In addition, the essential oils from aerial parts of <em>T. lamiifolium</em> subsp. <em>stachyophyllum</em> and <em>T. lamiifolium</em> subsp. <em>lamiifolium</em> were isolated by steam distillation and analysed by gas chromatography (GC) and gas chromatography–mass spectrometry (GC–MS). The major components were characterized as β-caryophyllene (23.5–44.8%), trans-β-bergamotene (22.4–26.4%), germacrene D (22.2%) and (Z)-β-farnesene (14.0%) for subp. <em>lamiifolium</em> and trans-β-bergamotene (38.1–41.1%) and β-caryophyllene (8.7–8.9%) for subsp. <em>stachyophyllum</em>, respectively. As a result of the studies, it is proposed that the taxon treated as <em>T. lamiifolium</em> subsp. <em>stachyophyllum</em> in the Turkish flora should be raised to specific rank as <em>T. stachyophyllum.</em></p></div>
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Teucrium stachyophyllum P. H. Davis was first described as a separate species in the ‘Syrian, Lebanon and Palestine Flora’, but was reduced to a subspecies of T. lamiifolium d’Urv. in the ‘Turkish Flora’. Studies on the macro- and micro-morphology as well as the anatomy of populations of T. lamiifolium subsp. stachyophyllum (P. H. Davis) Hedge &amp; Ekim and T. lamiifolium subsp. lamiifolium in Turkey have been carried out based on herbarium specimens and field observations. The results from the anatomical studies on stems and leaves show that although the two taxa are similar in stem anatomy, they differ in terms of mesophyll thickness and occurrence of crystals in the upper epidermal cells of the leaf. Light and scanning electron microscope analyzes revealed striking differences in colour, size, sculpture and gland density between nutlets of the two taxa. Morphological studies also showed that there were important differences between the two taxa in terms of inflorescence, indumentum, and stem length and thickness. In addition, the essential oils from aerial parts of T. lamiifolium subsp. stachyophyllum and T. lamiifolium subsp. lamiifolium were isolated by steam distillation and analysed by gas chromatography (GC) and gas chromatography–mass spectrometry (GC–MS). The major components were characterized as β-caryophyllene (23.5–44.8%), trans-β-bergamotene (22.4–26.4%), germacrene D (22.2%) and (Z)-β-farnesene (14.0%) for subp. lamiifolium and trans-β-bergamotene (38.1–41.1%) and β-caryophyllene (8.7–8.9%) for subsp. stachyophyllum, respectively. As a result of the studies, it is proposed that the taxon treated as T. lamiifolium subsp. stachyophyllum in the Turkish flora should be raised to specific rank as T. stachyophyllum.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01535.x" xmlns="http://purl.org/rss/1.0/"><title> Hedysarum kalatense sp. nov. (Fabaceae) from Iran</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01535.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Hedysarum kalatense sp. nov. (Fabaceae) from Iran</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. M. Dehshiri</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-06-27T09:14:25.406292-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01535.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.1756-1051.2012.01535.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01535.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">208</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">212</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><em>Hedysarum kalatense</em> Dehshiri sp. nov. (Fabaceae) is described and illustrated from Khorassan, Iran. It belongs to sect. <em>Crinifera</em> and is distinct among Iranian species. This species appears to be closely related to <em>H. macranthum</em> (Freyn &amp; Sint.) B. Fedtschenko. The diagnostic characters, as well as a full description and a detailed illustration are provided. <em>Hedysarum kalatense</em> is evaluated as ‘Vulnerable’ (VU) according to IUCN red list criteria.</p></div>
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Hedysarum kalatense Dehshiri sp. nov. (Fabaceae) is described and illustrated from Khorassan, Iran. It belongs to sect. Crinifera and is distinct among Iranian species. This species appears to be closely related to H. macranthum (Freyn &amp; Sint.) B. Fedtschenko. The diagnostic characters, as well as a full description and a detailed illustration are provided. Hedysarum kalatense is evaluated as ‘Vulnerable’ (VU) according to IUCN red list criteria.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01633.x" xmlns="http://purl.org/rss/1.0/"><title>What is Ornithogalum canaliculatum? New data on the African genus Stellarioides (Hyacinthaceae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01633.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">What is Ornithogalum canaliculatum? New data on the African genus Stellarioides (Hyacinthaceae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mario Martínez-Azorín, Manuel B. Crespo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-06-27T09:15:53.661012-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01633.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.1756-1051.2012.01633.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01633.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">213</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">221</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>In the frame of a taxonomic revision of <em>Stellarioides</em> Medik. we report here new data on the identity of <em>Ornithogalum canaliculatum</em> Lag. After studying natural populations and herbarium collections of <em>Stellarioides</em> Medik. from Africa, data supporting the synonymisation of <em>O. canaliculatum</em> Lag. to <em>Stellarioides sessiliflora</em> (Desf.) Speta are provided. A complete description is presented for this species, and data on typification, biology, habitat, and distribution are also included. Moreover, the new combination <em>Stellarioides lebaense</em> (Van Jaarsveld) Mart.-Azorín &amp; M. B. Crespo, is provided to accommodate the recently described <em>Ornithogalum lebaense</em> Van Jaarsveld from Angola.</p></div>
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In the frame of a taxonomic revision of Stellarioides Medik. we report here new data on the identity of Ornithogalum canaliculatum Lag. After studying natural populations and herbarium collections of Stellarioides Medik. from Africa, data supporting the synonymisation of O. canaliculatum Lag. to Stellarioides sessiliflora (Desf.) Speta are provided. A complete description is presented for this species, and data on typification, biology, habitat, and distribution are also included. Moreover, the new combination Stellarioides lebaense (Van Jaarsveld) Mart.-Azorín &amp; M. B. Crespo, is provided to accommodate the recently described Ornithogalum lebaense Van Jaarsveld from Angola.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01612.x" xmlns="http://purl.org/rss/1.0/"><title>Lectotypification of the Linnaean name Hypochaeris maculata (Asteraceae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01612.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Lectotypification of the Linnaean name Hypochaeris maculata (Asteraceae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Duilio Iamonico</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-07T10:34:40.201838-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01612.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.1756-1051.2012.01612.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01612.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">222</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">224</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>The typification of the name <em>Hypochaeris maculata</em> L. is discussed. A specimen from the Linnaean Herbarium (LINN) is designated as the lectotype.</p></div>
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The typification of the name Hypochaeris maculata L. is discussed. A specimen from the Linnaean Herbarium (LINN) is designated as the lectotype.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01388.x" xmlns="http://purl.org/rss/1.0/"><title>Ecological and biodiversity gradients across alpine dry grassland habitats: implications for an endangered species</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01388.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ecological and biodiversity gradients across alpine dry grassland habitats: implications for an endangered species</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Gilardelli, R. Gentili, F. Prosser, C. Bonomi, C. Varotto, S. Sgorbati</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-09T04:28:06.94418-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01388.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.1756-1051.2012.01388.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01388.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">225</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">238</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Dry grasslands are of great interest for nature conservation in Europe, because they have a central role in the conservation of numerous rare and endangered species. In this study carried out in the Brenta mountain group (Italian alps), we investigated the effect of environmental factors mainly controlled by topography, on the biodiversity trends across different dry grassland habitats where the threatened alpine stenoendemic <em>Erysimum aurantiacum</em> grows. Plant community data and ecological factors were analysed by means of a multi-habitat CCA approach and by analysis of biodiversity gradients in 7 natural and semi-natural habitats. We found that species turnover and biodiversity patterns vary as a function of multi-factorial ecological gradients. For the single habitats, elevation gradient was the main factor explaining compositional variation, followed by inclination and proportion of exposed rock surface. Despite its endangered status, <em>E. aurantiacum</em> showed a relatively high degree of ecological plasticity across these semiarid grassland habitats that probably allows it to survive in different environments, including in some cases those impacted by human activities. This prompts for habitat- more than species-level conservation actions. According to their characteristics and threats, habitat-specific management practices are recommended for long term conservation of plant species communities in the different ecological niches.</p></div>
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Dry grasslands are of great interest for nature conservation in Europe, because they have a central role in the conservation of numerous rare and endangered species. In this study carried out in the Brenta mountain group (Italian alps), we investigated the effect of environmental factors mainly controlled by topography, on the biodiversity trends across different dry grassland habitats where the threatened alpine stenoendemic Erysimum aurantiacum grows. Plant community data and ecological factors were analysed by means of a multi-habitat CCA approach and by analysis of biodiversity gradients in 7 natural and semi-natural habitats. We found that species turnover and biodiversity patterns vary as a function of multi-factorial ecological gradients. For the single habitats, elevation gradient was the main factor explaining compositional variation, followed by inclination and proportion of exposed rock surface. Despite its endangered status, E. aurantiacum showed a relatively high degree of ecological plasticity across these semiarid grassland habitats that probably allows it to survive in different environments, including in some cases those impacted by human activities. This prompts for habitat- more than species-level conservation actions. According to their characteristics and threats, habitat-specific management practices are recommended for long term conservation of plant species communities in the different ecological niches.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01211.x" xmlns="http://purl.org/rss/1.0/"><title>Low soil temperature inhibits the stimulatory effect of elevated [CO2] on height and biomass accumulation of white birch seedlings grown under three non-limiting phosphorus conditions</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01211.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Low soil temperature inhibits the stimulatory effect of elevated [CO2] on height and biomass accumulation of white birch seedlings grown under three non-limiting phosphorus conditions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Titus Fondo Ambebe, Gabriel Danyagri, Qing-Lai Dang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T09:09:15.49954-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01211.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.1756-1051.2012.01211.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01211.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">239</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">246</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>White birch (<em>Betula papyrifera</em> Marsh.) seedlings were exposed to ambient or doubled ambient carbon dioxide concentration ([CO<sub>2</sub>]), three soil temperatures (<em>T</em><sub>soil</sub>) (low, intermediate, high), and three phosphorus (P) regimes (low, medium, high) in environment-controlled greenhouses. Height (<em>H</em>), root-collar diameter (RCD), biomass, and leaf phosphorus concentration (leaf P) were determined four months after initiation of treatments. The low <em>T</em><sub>soil</sub> reduced <em>H</em>, RCD, shoot biomass, root biomass and total seedling biomass whereas the high-P level and the [CO<sub>2</sub>] elevation increased all the growth and biomass parameters. Elevated [CO<sub>2</sub>] significantly reduced leaf P. There were significant two-factor interactions suggesting that the effect of elevated [CO<sub>2</sub>] on (1) <em>H</em>, total biomass, biomass of plant components, and leaf P was dependent on <em>T</em><sub>soil</sub>, (2) total biomass was contingent on P regime. For instance, the positive response of <em>H</em> and total biomass to elevated [CO<sub>2</sub>] was limited to seedlings raised under the intermediate and high <em>T</em><sub>soil</sub>, respectively. In addition, [CO<sub>2</sub>] elevation increased total biomass only at the high-P regime but not at the low- or medium-P level where the effect of [CO<sub>2</sub>] was statistically insignificant. No significant main effect of treatment or interaction was observed for root to shoot biomass ratio.</p></div>
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White birch (Betula papyrifera Marsh.) seedlings were exposed to ambient or doubled ambient carbon dioxide concentration ([CO2]), three soil temperatures (Tsoil) (low, intermediate, high), and three phosphorus (P) regimes (low, medium, high) in environment-controlled greenhouses. Height (H), root-collar diameter (RCD), biomass, and leaf phosphorus concentration (leaf P) were determined four months after initiation of treatments. The low Tsoil reduced H, RCD, shoot biomass, root biomass and total seedling biomass whereas the high-P level and the [CO2] elevation increased all the growth and biomass parameters. Elevated [CO2] significantly reduced leaf P. There were significant two-factor interactions suggesting that the effect of elevated [CO2] on (1) H, total biomass, biomass of plant components, and leaf P was dependent on Tsoil, (2) total biomass was contingent on P regime. For instance, the positive response of H and total biomass to elevated [CO2] was limited to seedlings raised under the intermediate and high Tsoil, respectively. In addition, [CO2] elevation increased total biomass only at the high-P regime but not at the low- or medium-P level where the effect of [CO2] was statistically insignificant. No significant main effect of treatment or interaction was observed for root to shoot biomass ratio.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01511.x" xmlns="http://purl.org/rss/1.0/"><title>Effects of grazing and fertilization on the relationship between species abundance and functional traits in an alpine meadow community on the Tibetan Plateau</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01511.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effects of grazing and fertilization on the relationship between species abundance and functional traits in an alpine meadow community on the Tibetan Plateau</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wei Li, Fu-Ping Tian, Zheng-Wei Ren, Hai-Zhou Huang, Zhi-Nan Zhang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T09:18:28.224361-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2012.01511.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.1756-1051.2012.01511.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2012.01511.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">247</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">255</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Trait-based approaches can provide a useful tool for linking plant attributes to community structure and ecosystem function. Seed mass and plant height play important roles in the dynamics of plant communities, but few empirical community level studies have tested this, especially in stressful environments. The aim of the present study was to determine if there is a relationship between functional traits (seed mass and plant height) and changes in species relative abundance (SRA) in response to grazing and fertilization. We measured SRA and plant functional traits for 40 common species in a Tibetan Plateau alpine meadow. In the fertilized meadow, seed mass and plant height was significantly positively correlated with the relative abundance of the species. In the grazed meadow, these variables were significantly negatively correlated. Our results demonstrates that plant functional traits can be used to predict the change of SRA in plant community. Grazing promotes the dominance of small-seeded and short-stature species, and fertilization facilitates the occurrence of large-seeded and tall-stature species.</p></div>
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Trait-based approaches can provide a useful tool for linking plant attributes to community structure and ecosystem function. Seed mass and plant height play important roles in the dynamics of plant communities, but few empirical community level studies have tested this, especially in stressful environments. The aim of the present study was to determine if there is a relationship between functional traits (seed mass and plant height) and changes in species relative abundance (SRA) in response to grazing and fertilization. We measured SRA and plant functional traits for 40 common species in a Tibetan Plateau alpine meadow. In the fertilized meadow, seed mass and plant height was significantly positively correlated with the relative abundance of the species. In the grazed meadow, these variables were significantly negatively correlated. Our results demonstrates that plant functional traits can be used to predict the change of SRA in plant community. Grazing promotes the dominance of small-seeded and short-stature species, and fertilization facilitates the occurrence of large-seeded and tall-stature species.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2013.00295.x" xmlns="http://purl.org/rss/1.0/"><title>Addendum to ‘A new taxonomy of the family Teloschistaceae’</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2013.00295.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Addendum to ‘A new taxonomy of the family Teloschistaceae’</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ulf Arup, Ulrik Søchting, Patrik Frödén</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T09:09:15.49954-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1756-1051.2013.00295.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.1756-1051.2013.00295.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1756-1051.2013.00295.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">256</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">256</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>The recently invalidly published name Teloschistaceae subfam. Teloschistoideae Arup, Søchting &amp; Frödén subfam. nov. is validated here by providing a diagnosis for the taxon (ICN Art. 38).</p></div>
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The recently invalidly published name Teloschistaceae subfam. Teloschistoideae Arup, Søchting &amp; Frödén subfam. nov. is validated here by providing a diagnosis for the taxon (ICN Art. 38).
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