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            type="text/xsl"?><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)1752-4571" xmlns="http://purl.org/rss/1.0/"><title>Evolutionary Applications</title><description> Wiley Online Library : Evolutionary Applications</description><link>http://dx.doi.org/10.1111%2F%28ISSN%291752-4571</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/">© Blackwell Publishing Ltd</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1752-4571</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1752-4571</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">January 2012</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">5</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">101</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/eva.2012.5.issue-1/asset/cover.gif?v=1&amp;s=a91aa852d493476317c5ca14b35c787af328b9de"/><items><rdf:Seq><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00248.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00245.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00240.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00244.x"/><rdf:li 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rdf:resource="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00211.x"/></rdf:Seq></items></channel><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00248.x" xmlns="http://purl.org/rss/1.0/"><title>Evolutionary dynamics of separate and combined exposure of Pseudomonas fluorescens SBW25 to antibiotics and bacteriophage</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00248.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evolutionary dynamics of separate and combined exposure of Pseudomonas fluorescens SBW25 to antibiotics and bacteriophage</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Patricia Escobar-Páramo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Claire Gougat-Barbera</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael E. Hochberg</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-23T00:54:49.732837-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00248.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.1752-4571.2012.00248.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00248.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The use of bacteriophages against pathogenic bacteria in health care and in the food industry is now being advocated as an alternative to the use of antibiotics. But what is the evolutionary response for a bacterial population if both antibiotics and phages are used in combination? We employ an experimental evolution approach to address these questions and exposed <em>Pseudomonas fluorescens</em> SBW25 and a related hypermutator strain (<em>mutS</em>−) to the action of the antibiotic rifampicin and the lytic bacteriophage SBW25ϕ2. We then compared the densities, growth rates, and the mutations at the <em>rpoB</em> locus leading to rifampicin resistance of the evolved bacterial populations. We observed that the evolutionary response of populations under different treatments varied depending on the order in which the antimicrobials were added and whether the bacterium was a hypermutator. We found that wild-type rifampicin-resistant populations involved in biofilm formation often reverted to rifampicin sensitivity when stresses were added sequentially. In contrast, when the mortality agents were added simultaneously, phage populations frequently went extinct and the bacteria evolved antibiotic resistance. However, populations of the hypermutator <em>mutS</em>− converged to a single genotype at the <em>rpoB</em> locus. Future investigation on other bacteria and using different antibiotics and bacteriophage are needed to evaluate the generality of our findings.</p></div>]]></content:encoded><description>The use of bacteriophages against pathogenic bacteria in health care and in the food industry is now being advocated as an alternative to the use of antibiotics. But what is the evolutionary response for a bacterial population if both antibiotics and phages are used in combination? We employ an experimental evolution approach to address these questions and exposed Pseudomonas fluorescens SBW25 and a related hypermutator strain (mutS−) to the action of the antibiotic rifampicin and the lytic bacteriophage SBW25ϕ2. We then compared the densities, growth rates, and the mutations at the rpoB locus leading to rifampicin resistance of the evolved bacterial populations. We observed that the evolutionary response of populations under different treatments varied depending on the order in which the antimicrobials were added and whether the bacterium was a hypermutator. We found that wild-type rifampicin-resistant populations involved in biofilm formation often reverted to rifampicin sensitivity when stresses were added sequentially. In contrast, when the mortality agents were added simultaneously, phage populations frequently went extinct and the bacteria evolved antibiotic resistance. However, populations of the hypermutator mutS− converged to a single genotype at the rpoB locus. Future investigation on other bacteria and using different antibiotics and bacteriophage are needed to evaluate the generality of our findings.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00245.x" xmlns="http://purl.org/rss/1.0/"><title>Life history change in response to fishing and an introduced predator in the East African cyprinid Rastrineobola argentea</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00245.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Life history change in response to fishing and an introduced predator in the East African cyprinid Rastrineobola argentea</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Diana M. T. Sharpe</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Silvester B. Wandera</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lauren J. Chapman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-23T00:53:13.105598-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00245.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.1752-4571.2012.00245.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00245.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Fishing and introduced species are among the most important stressors affecting freshwaters and can also be strong selective agents. We examined the combined effects of commercial fishing and an introduced predator (Nile perch, <em>Lates niloticus</em>) on life history traits in an African cyprinid fish (<em>Rastrineobola argentea</em>) native to the Lake Victoria basin in East Africa. To understand whether these two stressors have driven shifts in life history traits of <em>R. argentea</em>, we tested for associations between life history phenotypes and the presence/absence of stressors both spatially (across 10 Ugandan lakes) and temporally (over four decades in Lake Victoria). Overall, introduced Nile perch and fishing tended to be associated with a suite of life history responses in <em>R. argentea</em>, including: decreased body size, maturation at smaller sizes, and increased reproductive effort (larger eggs; and higher relative fecundity, clutch volume, and ovary weight). This is one of the first well-documented examples of fisheries-induced phenotypic change in a tropical, freshwater stock; the magnitude of which raises some concerns for the long-term sustainability of this fishery, now the most important (by mass) in Lake Victoria.</p></div>]]></content:encoded><description>Fishing and introduced species are among the most important stressors affecting freshwaters and can also be strong selective agents. We examined the combined effects of commercial fishing and an introduced predator (Nile perch, Lates niloticus) on life history traits in an African cyprinid fish (Rastrineobola argentea) native to the Lake Victoria basin in East Africa. To understand whether these two stressors have driven shifts in life history traits of R. argentea, we tested for associations between life history phenotypes and the presence/absence of stressors both spatially (across 10 Ugandan lakes) and temporally (over four decades in Lake Victoria). Overall, introduced Nile perch and fishing tended to be associated with a suite of life history responses in R. argentea, including: decreased body size, maturation at smaller sizes, and increased reproductive effort (larger eggs; and higher relative fecundity, clutch volume, and ovary weight). This is one of the first well-documented examples of fisheries-induced phenotypic change in a tropical, freshwater stock; the magnitude of which raises some concerns for the long-term sustainability of this fishery, now the most important (by mass) in Lake Victoria.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00240.x" xmlns="http://purl.org/rss/1.0/"><title>Genomic regions in crop–wild hybrids of lettuce are affected differently in different environments: implications for crop breeding</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00240.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genomic regions in crop–wild hybrids of lettuce are affected differently in different environments: implications for crop breeding</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yorike Hartman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Danny A. P. Hooftman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Brigitte Uwimana</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Clemens C. M. van de Wiel</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marinus J. M. Smulders</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Richard G. F. Visser</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter H. van Tienderen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-23T00:52:35.902531-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00240.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.1752-4571.2012.00240.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00240.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Many crops contain domestication genes that are generally considered to lower fitness of crop–wild hybrids in the wild environment. Transgenes placed in close linkage with such genes would be less likely to spread into a wild population. Therefore, for environmental risk assessment of GM crops, it is important to know whether genomic regions with such genes exist, and how they affect fitness. We performed quantitative trait loci (QTL) analyses on fitness(-related) traits in two different field environments employing recombinant inbred lines from a cross between cultivated <em>Lactuca sativa</em> and its wild relative <em>Lactuca serriola</em>. We identified a region on linkage group 5 where the crop allele consistently conferred a selective advantage (increasing fitness to 212% and 214%), whereas on linkage group 7, a region conferred a selective disadvantage (reducing fitness to 26% and 5%), mainly through delaying flowering. The probability for a putative transgene spreading would therefore depend strongly on the insertion location. Comparison of these field results with greenhouse data from a previous study using the same lines showed considerable differences in QTL patterns. This indicates that care should be taken when extrapolating experiments from the greenhouse, and that the impact of domestication genes has to be assessed under field conditions.</p></div>]]></content:encoded><description>Many crops contain domestication genes that are generally considered to lower fitness of crop–wild hybrids in the wild environment. Transgenes placed in close linkage with such genes would be less likely to spread into a wild population. Therefore, for environmental risk assessment of GM crops, it is important to know whether genomic regions with such genes exist, and how they affect fitness. We performed quantitative trait loci (QTL) analyses on fitness(-related) traits in two different field environments employing recombinant inbred lines from a cross between cultivated Lactuca sativa and its wild relative Lactuca serriola. We identified a region on linkage group 5 where the crop allele consistently conferred a selective advantage (increasing fitness to 212% and 214%), whereas on linkage group 7, a region conferred a selective disadvantage (reducing fitness to 26% and 5%), mainly through delaying flowering. The probability for a putative transgene spreading would therefore depend strongly on the insertion location. Comparison of these field results with greenhouse data from a previous study using the same lines showed considerable differences in QTL patterns. This indicates that care should be taken when extrapolating experiments from the greenhouse, and that the impact of domestication genes has to be assessed under field conditions.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00244.x" xmlns="http://purl.org/rss/1.0/"><title>Gene flow networks among American Aedes aegypti populations</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00244.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Gene flow networks among American Aedes aegypti populations</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anders Gonçalves da Silva</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ivana C. L. Cunha</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Walter S. Santos</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sérgio L. B. Luz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paulo E. M. Ribolla</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fernando Abad-Franch</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-15T21:59:54.937516-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00244.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.1752-4571.2012.00244.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00244.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The mosquito <em>Aedes aegypti</em>, the dengue virus vector, has spread throughout the tropics in historical times. While this suggests man-mediated dispersal, estimating contemporary connectivity among populations has remained elusive. Here, we use a large mtDNA dataset and a Bayesian coalescent framework to test a set of hypotheses about gene flow among American <em>Ae. aegypti</em> populations. We assessed gene flow patterns at the continental and subregional (Amazon basin) scales. For the Americas, our data favor a stepping-stone model in which gene flow is higher among adjacent populations but in which, at the same time, North American and southeastern Brazilian populations are directly connected, likely via sea trade. Within Amazonia, the model with highest support suggests extensive gene flow among major cities; Manaus, located at the center of the subregional transport network, emerges as a potentially important connecting hub. Our results suggest substantial connectivity across <em>Ae. aegypti</em> populations in the Americas. As long-distance active dispersal has not been observed in this species, our data support man-mediated dispersal as a major determinant of the genetic structure of American <em>Ae. aegypti</em> populations. The inferred topology of interpopulation connectivity can inform network models of <em>Ae. aegypti</em> and dengue spread.</p></div>]]></content:encoded><description>The mosquito Aedes aegypti, the dengue virus vector, has spread throughout the tropics in historical times. While this suggests man-mediated dispersal, estimating contemporary connectivity among populations has remained elusive. Here, we use a large mtDNA dataset and a Bayesian coalescent framework to test a set of hypotheses about gene flow among American Ae. aegypti populations. We assessed gene flow patterns at the continental and subregional (Amazon basin) scales. For the Americas, our data favor a stepping-stone model in which gene flow is higher among adjacent populations but in which, at the same time, North American and southeastern Brazilian populations are directly connected, likely via sea trade. Within Amazonia, the model with highest support suggests extensive gene flow among major cities; Manaus, located at the center of the subregional transport network, emerges as a potentially important connecting hub. Our results suggest substantial connectivity across Ae. aegypti populations in the Americas. As long-distance active dispersal has not been observed in this species, our data support man-mediated dispersal as a major determinant of the genetic structure of American Ae. aegypti populations. The inferred topology of interpopulation connectivity can inform network models of Ae. aegypti and dengue spread.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00246.x" xmlns="http://purl.org/rss/1.0/"><title>Evolution of pathogenicity traits in the apple scab fungal pathogen in response to the domestication of its host</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00246.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evolution of pathogenicity traits in the apple scab fungal pathogen in response to the domestication of its host</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Amandine Lê Van</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pierre Gladieux</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christophe Lemaire</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Amandine Cornille</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tatiana Giraud</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Charles-Eric Durel</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Valérie Caffier</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bruno Le Cam</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-15T21:59:47.615865-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00246.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.1752-4571.2012.00246.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00246.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Understanding how pathogens emerge is essential to bring disease-causing agents under durable human control. Here, we used cross-pathogenicity tests to investigate the changes in life-history traits of the fungal pathogen <em>Venturia inaequalis</em> associated with host-tracking during the domestication of apple and subsequent host-range expansion on the wild European crabapple (<em>Malus sylvestris</em>). Pathogenicity of 40 isolates collected in wild and domesticated ecosystems was assessed on the domesticated apple, its Central Asian main progenitor (<em>M</em>.<em> sieversii</em>) and <em>M. sylvestris</em>. Isolates from wild habitats in the centre of origin of the crop were not pathogenic on the domesticated apple and less aggressive than other isolates on their host of origin. Isolates from the agro-ecosystem in Central Asia infected a higher proportion of plants with higher aggressiveness, on both the domesticated host and its progenitor. Isolates from the European crabapple were still able to cause disease on other species but were less aggressive and less frequently virulent on these hosts than their endemic populations. Our results suggest that the domestication of apple was associated with the acquisition of virulence in the pathogen following host-tracking. The spread of the disease in the agro-ecosystem would also have been accompanied by an increase in overall pathogenicity.</p></div>]]></content:encoded><description>Understanding how pathogens emerge is essential to bring disease-causing agents under durable human control. Here, we used cross-pathogenicity tests to investigate the changes in life-history traits of the fungal pathogen Venturia inaequalis associated with host-tracking during the domestication of apple and subsequent host-range expansion on the wild European crabapple (Malus sylvestris). Pathogenicity of 40 isolates collected in wild and domesticated ecosystems was assessed on the domesticated apple, its Central Asian main progenitor (M. sieversii) and M. sylvestris. Isolates from wild habitats in the centre of origin of the crop were not pathogenic on the domesticated apple and less aggressive than other isolates on their host of origin. Isolates from the agro-ecosystem in Central Asia infected a higher proportion of plants with higher aggressiveness, on both the domesticated host and its progenitor. Isolates from the European crabapple were still able to cause disease on other species but were less aggressive and less frequently virulent on these hosts than their endemic populations. Our results suggest that the domestication of apple was associated with the acquisition of virulence in the pathogen following host-tracking. The spread of the disease in the agro-ecosystem would also have been accompanied by an increase in overall pathogenicity.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00243.x" xmlns="http://purl.org/rss/1.0/"><title>The response of correlated traits following cessation of fishery-induced selection</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00243.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The response of correlated traits following cessation of fishery-induced selection</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Santiago Salinas</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kestrel O. Perez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tara A. Duffy</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stephen J. Sabatino</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lyndie A. Hice</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stephan B. Munch</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David O. Conover</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-15T21:57:36.362164-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00243.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.1752-4571.2012.00243.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00243.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The application of evolutionary principles to the management of fisheries has gained considerable attention recently. Harvesting of fish may apply directional or disruptive selection to key life-history traits, and evidence for fishery-induced evolution is growing. The traits that are directly selected upon are often correlated (genetically or phenotypically) with a suite of interrelated physiological, behavioral, and morphological characters. A question that has received comparatively little attention is whether or not, after cessation of fishery-induced selection, these correlated traits revert back to previous states. Here, we empirically examine this question. In experiments with the Atlantic silverside, <em>Menidia menidia</em>, we applied size-selective culling for five generations and then maintained the lines a further five generations under random harvesting. We found that some traits do return to preharvesting levels (e.g., larval viability), some partially recover (e.g., egg volume, size-at-hatch), and others show no sign of change (e.g., food consumption rate, vertebral number). Such correlations among characters could, in theory, greatly accelerate or decelerate the recovery of fish populations. These results may explain why some fish stocks fail to recover after fishing pressure is relaxed.</p></div>]]></content:encoded><description>The application of evolutionary principles to the management of fisheries has gained considerable attention recently. Harvesting of fish may apply directional or disruptive selection to key life-history traits, and evidence for fishery-induced evolution is growing. The traits that are directly selected upon are often correlated (genetically or phenotypically) with a suite of interrelated physiological, behavioral, and morphological characters. A question that has received comparatively little attention is whether or not, after cessation of fishery-induced selection, these correlated traits revert back to previous states. Here, we empirically examine this question. In experiments with the Atlantic silverside, Menidia menidia, we applied size-selective culling for five generations and then maintained the lines a further five generations under random harvesting. We found that some traits do return to preharvesting levels (e.g., larval viability), some partially recover (e.g., egg volume, size-at-hatch), and others show no sign of change (e.g., food consumption rate, vertebral number). Such correlations among characters could, in theory, greatly accelerate or decelerate the recovery of fish populations. These results may explain why some fish stocks fail to recover after fishing pressure is relaxed.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00242.x" xmlns="http://purl.org/rss/1.0/"><title>Scanning SNPs from a large set of expressed genes to assess the impact of artificial selection on the undomesticated genetic diversity of white spruce</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00242.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Scanning SNPs from a large set of expressed genes to assess the impact of artificial selection on the undomesticated genetic diversity of white spruce</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marie-Claire Namroud</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jean Bousquet</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Trevor Doerksen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jean Beaulieu</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-07T08:21:11.48493-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00242.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.1752-4571.2012.00242.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00242.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A scan involving 1134 single-nucleotide polymorphisms (SNPs) from 709 expressed genes was used to assess the potential impact of artificial selection for height growth on the genetic diversity of white spruce. Two case populations of different sizes simulating different family selection intensities (<em>K </em>=<em> </em>13% and 5%, respectively) were delineated from the Quebec breeding program. Their genetic diversity and allele frequencies were compared with those of control populations of the same size and geographic origin to assess the effect of increasing the selection intensity. The two control populations were also compared to assess the effect of reducing the sampling size. On one hand, in all pairwise comparisons, genetic diversity parameters were comparable and no alleles were lost in the case populations compared with the control ones, except for few rare alleles in the large case population. Also, the distribution of allele frequencies did not change significantly (<em>P </em>≤<em> </em>0.05) between the populations compared, but ten and nine SNPs (0.8%) exhibited significant differences in frequency (<em>P </em>≤<em> </em>0.01) between case and control populations of large and small sizes, respectively. Results of association tests between breeding values for height at 15 years of age and these SNPs supported the hypothesis of a potential effect of selection on the genes harboring these SNPs. On the other hand, contrary to expectations, there was no evidence that selection induced an increase in linkage disequilibrium in genes potentially affected by selection. These results indicate that neither the reduction in the sampling size nor the increase in selection intensity was sufficient to induce a significant change in the genetic diversity of the selected populations. Apparently, no loci were under strong selection pressure, confirming that the genetic control of height growth in white spruce involves many genes with small effects. Hence, selection for height growth at the present intensities did not appear to compromise background genetic diversity but, as predicted by theory, effects were detected at a few gene SNPs harboring intermediate allele frequencies.</p></div>]]></content:encoded><description>A scan involving 1134 single-nucleotide polymorphisms (SNPs) from 709 expressed genes was used to assess the potential impact of artificial selection for height growth on the genetic diversity of white spruce. Two case populations of different sizes simulating different family selection intensities (K = 13% and 5%, respectively) were delineated from the Quebec breeding program. Their genetic diversity and allele frequencies were compared with those of control populations of the same size and geographic origin to assess the effect of increasing the selection intensity. The two control populations were also compared to assess the effect of reducing the sampling size. On one hand, in all pairwise comparisons, genetic diversity parameters were comparable and no alleles were lost in the case populations compared with the control ones, except for few rare alleles in the large case population. Also, the distribution of allele frequencies did not change significantly (P ≤ 0.05) between the populations compared, but ten and nine SNPs (0.8%) exhibited significant differences in frequency (P ≤ 0.01) between case and control populations of large and small sizes, respectively. Results of association tests between breeding values for height at 15 years of age and these SNPs supported the hypothesis of a potential effect of selection on the genes harboring these SNPs. On the other hand, contrary to expectations, there was no evidence that selection induced an increase in linkage disequilibrium in genes potentially affected by selection. These results indicate that neither the reduction in the sampling size nor the increase in selection intensity was sufficient to induce a significant change in the genetic diversity of the selected populations. Apparently, no loci were under strong selection pressure, confirming that the genetic control of height growth in white spruce involves many genes with small effects. Hence, selection for height growth at the present intensities did not appear to compromise background genetic diversity but, as predicted by theory, effects were detected at a few gene SNPs harboring intermediate allele frequencies.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00241.x" xmlns="http://purl.org/rss/1.0/"><title>Demographic history of an elusive carnivore: using museums to inform management</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00241.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Demographic history of an elusive carnivore: using museums to inform management</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joseph D. Holbrook</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Randy W. DeYoung</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael E. Tewes</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">John H. Young</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-07T08:20:48.307548-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00241.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.1752-4571.2012.00241.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00241.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Elusive carnivores present a challenge to managers because traditional survey methods are not suitable. We applied a genetic approach using museum specimens to examine how historical and recent conditions influenced the demographic history of <em>Puma concolor</em> in western and southern Texas, USA. We used 10 microsatellite loci and indexed population trends by estimating historical and recent genetic diversity, genetic differentiation and effective population size. Mountain lions in southern Texas exhibited a 9% decline in genetic diversity, whereas diversity remained stable in western Texas. Genetic differentiation between western and southern Texas was minimal historically (<em>F</em><sub>ST</sub> = 0.04, <em>P </em>&lt;<em> </em>0.01), but increased 2–2.5 times in our recent sample. An index of genetic drift for southern Texas was seven to eight times that of western Texas, presumably contributing to the current differentiation between western and southern Texas. Furthermore, southern Texas exhibited a <em>&gt;</em>50% temporal decline in effective population size, whereas western Texas showed no change. Our results illustrate that population declines and genetic drift have occurred in southern Texas, likely because of contemporary habitat loss and predator control. Population monitoring may be needed to ensure the persistence of mountain lions in the southern Texas region. This study highlights the utility of sampling museum collections to examine demographic histories and inform wildlife management.</p></div>]]></content:encoded><description>Elusive carnivores present a challenge to managers because traditional survey methods are not suitable. We applied a genetic approach using museum specimens to examine how historical and recent conditions influenced the demographic history of Puma concolor in western and southern Texas, USA. We used 10 microsatellite loci and indexed population trends by estimating historical and recent genetic diversity, genetic differentiation and effective population size. Mountain lions in southern Texas exhibited a 9% decline in genetic diversity, whereas diversity remained stable in western Texas. Genetic differentiation between western and southern Texas was minimal historically (FST = 0.04, P &lt; 0.01), but increased 2–2.5 times in our recent sample. An index of genetic drift for southern Texas was seven to eight times that of western Texas, presumably contributing to the current differentiation between western and southern Texas. Furthermore, southern Texas exhibited a &gt;50% temporal decline in effective population size, whereas western Texas showed no change. Our results illustrate that population declines and genetic drift have occurred in southern Texas, likely because of contemporary habitat loss and predator control. Population monitoring may be needed to ensure the persistence of mountain lions in the southern Texas region. This study highlights the utility of sampling museum collections to examine demographic histories and inform wildlife management.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00233.x" xmlns="http://purl.org/rss/1.0/"><title>Birds in space and time: genetic changes accompanying anthropogenic habitat fragmentation in the endangered black-capped vireo (Vireo atricapilla)</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00233.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Birds in space and time: genetic changes accompanying anthropogenic habitat fragmentation in the endangered black-capped vireo (Vireo atricapilla)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Giridhar Athrey</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kelly R. Barr</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Richard F. Lance</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paul L. Leberg</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-24T05:01:17.897169-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00233.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.1752-4571.2011.00233.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00233.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Anthropogenic alterations in the natural environment can be a potent evolutionary force. For species that have specific habitat requirements, habitat loss can result in substantial genetic effects, potentially impeding future adaptability and evolution. The endangered black-capped vireo (<em>Vireo atricapilla</em>) suffered a substantial contraction of breeding habitat and population size during much of the 20th century. In a previous study, we reported significant differentiation between remnant populations, but failed to recover a strong genetic signal of bottlenecks. In this study, we used a combination of historical and contemporary sampling from Oklahoma and Texas to (i) determine whether population structure and genetic diversity have changed over time and (ii) evaluate alternate demographic hypotheses using approximate Bayesian computation (ABC). We found lower genetic diversity and increased differentiation in contemporary samples compared to historical samples, indicating nontrivial impacts of fragmentation. ABC analysis suggests a bottleneck having occurred in the early part of the 20th century, resulting in a magnitude decline in effective population size. Genetic monitoring with temporally spaced samples, such as used in this study, can be highly informative for assessing the genetic impacts of anthropogenic fragmentation on threatened or endangered species, as well as revealing the dynamics of small populations over time.</p></div>]]></content:encoded><description>Anthropogenic alterations in the natural environment can be a potent evolutionary force. For species that have specific habitat requirements, habitat loss can result in substantial genetic effects, potentially impeding future adaptability and evolution. The endangered black-capped vireo (Vireo atricapilla) suffered a substantial contraction of breeding habitat and population size during much of the 20th century. In a previous study, we reported significant differentiation between remnant populations, but failed to recover a strong genetic signal of bottlenecks. In this study, we used a combination of historical and contemporary sampling from Oklahoma and Texas to (i) determine whether population structure and genetic diversity have changed over time and (ii) evaluate alternate demographic hypotheses using approximate Bayesian computation (ABC). We found lower genetic diversity and increased differentiation in contemporary samples compared to historical samples, indicating nontrivial impacts of fragmentation. ABC analysis suggests a bottleneck having occurred in the early part of the 20th century, resulting in a magnitude decline in effective population size. Genetic monitoring with temporally spaced samples, such as used in this study, can be highly informative for assessing the genetic impacts of anthropogenic fragmentation on threatened or endangered species, as well as revealing the dynamics of small populations over time.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00239.x" xmlns="http://purl.org/rss/1.0/"><title>Life history and demographic determinants of effective/census size ratios as exemplified by brown trout (Salmo trutta)</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00239.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Life history and demographic determinants of effective/census size ratios as exemplified by brown trout (Salmo trutta)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dimitar Serbezov</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Per Erik Jorde</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Louis Bernatchez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Esben Moland Olsen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leif Asbjørn Vøllestad</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-23T06:48:56.675608-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00239.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.1752-4571.2012.00239.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00239.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A number of demographic factors, many of which related to human-driven encroachments, are predicted to decrease the effective population size (<em>N</em><sub>e</sub>) relative to the census population size (<em>N</em>), but these have been little investigated. Yet, it is necessary to know which factors most strongly impact <em>N</em><sub>e</sub>, and how to mitigate these effects through sound management actions. In this study, we use parentage analysis of a stream-living brown trout (<em>Salmo trutta</em>) population to quantify the effect of between-individual variance in reproductive success on the effective number of breeders (<em>N</em><sub>b</sub>) relative to the census number of breeders (<em>N</em><sub>i</sub>). Comprehensive estimates of the <em>N</em><sub>b</sub><em>/N</em> ratio were reduced to 0.16–0.28, almost entirely due to larger than binomial variance in family size. We used computer simulations, based on empirical estimates of age-specific survival and fecundity rates, to assess the effect of repeat spawning (iteroparity) on <em>N</em><sub>e</sub> and found that the variance in lifetime reproductive success was substantially higher for repeat spawners. Random family-specific survival, on the other hand, acts to buffer these effects. We discuss the implications of these findings for the management of small populations, where maintaining high and stable levels of <em>N</em><sub>e</sub> is crucial to extenuate inbreeding and protect genetic variability.</p></div>]]></content:encoded><description>A number of demographic factors, many of which related to human-driven encroachments, are predicted to decrease the effective population size (Ne) relative to the census population size (N), but these have been little investigated. Yet, it is necessary to know which factors most strongly impact Ne, and how to mitigate these effects through sound management actions. In this study, we use parentage analysis of a stream-living brown trout (Salmo trutta) population to quantify the effect of between-individual variance in reproductive success on the effective number of breeders (Nb) relative to the census number of breeders (Ni). Comprehensive estimates of the Nb/N ratio were reduced to 0.16–0.28, almost entirely due to larger than binomial variance in family size. We used computer simulations, based on empirical estimates of age-specific survival and fecundity rates, to assess the effect of repeat spawning (iteroparity) on Ne and found that the variance in lifetime reproductive success was substantially higher for repeat spawners. Random family-specific survival, on the other hand, acts to buffer these effects. We discuss the implications of these findings for the management of small populations, where maintaining high and stable levels of Ne is crucial to extenuate inbreeding and protect genetic variability.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00238.x" xmlns="http://purl.org/rss/1.0/"><title>Genetic structure and rabies spread potential in raccoons: the role of landscape barriers and sex-biased dispersal</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00238.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genetic structure and rabies spread potential in raccoons: the role of landscape barriers and sex-biased dispersal</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Héloïse Côté</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dany Garant</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Karine Robert</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Julien Mainguy</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fanie Pelletier</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-23T06:48:42.596369-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00238.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.1752-4571.2012.00238.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00238.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Identifying natural barriers to movements of hosts associated with infectious diseases is essential for developing effective control strategies. Raccoon rabies variant (RRV) is a zoonosis of concern for humans because its main vector, the raccoon (<em>Procyon lotor</em>), is found near residential areas. In Québec, Canada, all cases of RRV found in raccoons since 2006 were detected on the eastern side of the Richelieu River, suggesting that this river acts as a barrier to gene flow and thus the potential for RRV to spread. The objectives of this study were to characterize the genetic structure of raccoon populations and assess the effect of the Richelieu River on the population structure in southern Québec, Canada. We also evaluated whether RRV spread potential differed between sex and at a larger spatial scale. Our analyses revealed a weak signal of genetic differentiation among individuals located on each side of the Richelieu River. At a larger spatial scale, genetic structuring was weak. Our results suggest that rivers might not always efficiently restrain raccoon movements and spread of RRV. We suggest that the difference in genetic structure found between sexes can be partly explained by male movements during the breeding season in winter, when ice bridges allow passage over most rivers in Québec.</p></div>]]></content:encoded><description>Identifying natural barriers to movements of hosts associated with infectious diseases is essential for developing effective control strategies. Raccoon rabies variant (RRV) is a zoonosis of concern for humans because its main vector, the raccoon (Procyon lotor), is found near residential areas. In Québec, Canada, all cases of RRV found in raccoons since 2006 were detected on the eastern side of the Richelieu River, suggesting that this river acts as a barrier to gene flow and thus the potential for RRV to spread. The objectives of this study were to characterize the genetic structure of raccoon populations and assess the effect of the Richelieu River on the population structure in southern Québec, Canada. We also evaluated whether RRV spread potential differed between sex and at a larger spatial scale. Our analyses revealed a weak signal of genetic differentiation among individuals located on each side of the Richelieu River. At a larger spatial scale, genetic structuring was weak. Our results suggest that rivers might not always efficiently restrain raccoon movements and spread of RRV. We suggest that the difference in genetic structure found between sexes can be partly explained by male movements during the breeding season in winter, when ice bridges allow passage over most rivers in Québec.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00237.x" xmlns="http://purl.org/rss/1.0/"><title>Phylogeny meets ecotoxicology: evolutionary patterns of sensitivity to a common insecticide</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00237.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Phylogeny meets ecotoxicology: evolutionary patterns of sensitivity to a common insecticide</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">John I. Hammond</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Devin K. Jones</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Patrick R. Stephens</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rick A. Relyea</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-23T05:57:50.639703-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00237.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.1752-4571.2011.00237.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00237.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Pesticides commonly occur in aquatic systems and pose a substantial challenge to the conservation of many taxa. Ecotoxicology has traditionally met this challenge by focusing on short-term, single-species tests and conducting risk assessments based on the most sensitive species tested. Rarely have ecotoxicology data been examined from an evolutionary perspective, and to our knowledge, there has never been a phylogenetic analysis of sensitivity, despite the fact that doing so would provide insights into patterns of sensitivity among species and identify which clades are the most sensitive to a particular pesticide. We examined phylogenetic patterns of pesticide sensitivity in amphibians, a group of conservation concern owing to global population declines. Using the insecticide endosulfan, we combined previously published results across seven species of tadpoles and added eight additional species from the families Bufonidae, Hylidae, and Ranidae. We found significant phylogenetic signal in the sensitivity to the insecticide and in the existence of time lag effects on tadpole mortality. Bufonids were less sensitive than hylids, which were less sensitive than the ranids. Moreover, mortality time lags were common in ranids, occasional in hylids, and rare in bufonids. These results highlight the importance of an evolutionary perspective and offer important insights for conservation.</p></div>]]></content:encoded><description>Pesticides commonly occur in aquatic systems and pose a substantial challenge to the conservation of many taxa. Ecotoxicology has traditionally met this challenge by focusing on short-term, single-species tests and conducting risk assessments based on the most sensitive species tested. Rarely have ecotoxicology data been examined from an evolutionary perspective, and to our knowledge, there has never been a phylogenetic analysis of sensitivity, despite the fact that doing so would provide insights into patterns of sensitivity among species and identify which clades are the most sensitive to a particular pesticide. We examined phylogenetic patterns of pesticide sensitivity in amphibians, a group of conservation concern owing to global population declines. Using the insecticide endosulfan, we combined previously published results across seven species of tadpoles and added eight additional species from the families Bufonidae, Hylidae, and Ranidae. We found significant phylogenetic signal in the sensitivity to the insecticide and in the existence of time lag effects on tadpole mortality. Bufonids were less sensitive than hylids, which were less sensitive than the ranids. Moreover, mortality time lags were common in ranids, occasional in hylids, and rare in bufonids. These results highlight the importance of an evolutionary perspective and offer important insights for conservation.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00236.x" xmlns="http://purl.org/rss/1.0/"><title>Phages limit the evolution of bacterial antibiotic resistance in experimental microcosms</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00236.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Phages limit the evolution of bacterial antibiotic resistance in experimental microcosms</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Quan-Guo Zhang</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Angus Buckling</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-13T02:43:58.084194-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00236.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.1752-4571.2011.00236.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00236.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The evolution of multi-antibiotic resistance in bacterial pathogens, often resulting from <em>de novo</em> mutations, is creating a public health crisis. Phages show promise for combating antibiotic-resistant bacteria, the efficacy of which, however, may also be limited by resistance evolution. Here, we suggest that phages may be used as supplements to antibiotics in treating initially sensitive bacteria to prevent resistance evolution, as phages are unaffected by most antibiotics and there should be little cross-resistance to antibiotics and phages. <em>In vitro</em> experiments using the bacterium <em>Pseudomonas fluorescens</em>, a lytic phage, and the antibiotic kanamycin supported this prediction: an antibiotic–phage combination dramatically decreased the chance of bacterial population survival that indicates resistance evolution, compared with antibiotic treatment alone, whereas the phage alone did not affect bacterial survival. This effect of the combined treatment in preventing resistance evolution was robust to immigration of bacteria from an untreated environment, but not to immigration from environment where the bacteria had coevolved with the phage. By contrast, an isogenic hypermutable strain constructed from the wild-type <em>P. fluorescens</em> evolved resistance to all treatments regardless of immigration, but typically suffered very large fitness costs. These results suggest that an antibiotic–phage combination may show promise as an antimicrobial strategy.</p></div>]]></content:encoded><description>The evolution of multi-antibiotic resistance in bacterial pathogens, often resulting from de novo mutations, is creating a public health crisis. Phages show promise for combating antibiotic-resistant bacteria, the efficacy of which, however, may also be limited by resistance evolution. Here, we suggest that phages may be used as supplements to antibiotics in treating initially sensitive bacteria to prevent resistance evolution, as phages are unaffected by most antibiotics and there should be little cross-resistance to antibiotics and phages. In vitro experiments using the bacterium Pseudomonas fluorescens, a lytic phage, and the antibiotic kanamycin supported this prediction: an antibiotic–phage combination dramatically decreased the chance of bacterial population survival that indicates resistance evolution, compared with antibiotic treatment alone, whereas the phage alone did not affect bacterial survival. This effect of the combined treatment in preventing resistance evolution was robust to immigration of bacteria from an untreated environment, but not to immigration from environment where the bacteria had coevolved with the phage. By contrast, an isogenic hypermutable strain constructed from the wild-type P. fluorescens evolved resistance to all treatments regardless of immigration, but typically suffered very large fitness costs. These results suggest that an antibiotic–phage combination may show promise as an antimicrobial strategy.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00235.x" xmlns="http://purl.org/rss/1.0/"><title>Genetic monitoring and complex population dynamics: insights from a 12-year study of the Rio Grande silvery minnow</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00235.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genetic monitoring and complex population dynamics: insights from a 12-year study of the Rio Grande silvery minnow</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Megan J. Osborne</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Evan W. Carson</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Thomas F. Turner</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-12T00:37:20.356882-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00235.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.1752-4571.2011.00235.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00235.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The endangered Rio Grande silvery minnow persists as a remnant population in a highly fragmented and regulated arid-land river system. The species is subject to dramatic annual fluctuations in density. Since 2003, the wild population has been supplemented by hatchery-reared fish. We report on a 12-year (1999–2010) monitoring study of genetic diversity and effective population size (<em>N</em><sub>e</sub>) of wild and hatchery stocks. Our goals were to evaluate how genetic metrics responded to changes in wild fish density and whether they corresponded to the number and levels of diversity of hatchery-reared repatriates. Genetic diversity and all measures of <em>N</em><sub>e</sub> in the wild population did not correlate with wild fish density until hatchery supplementation began in earnest. Estimates of variance and inbreeding effective size were not correlated. Our results suggest source–sink dynamics where captive stocks form a genetically diverse source and the wild population behaves as a sink. Nevertheless, overall genetic diversity of silvery minnow has been maintained over the last decade, and we attribute this to a well-designed and executed propagation management plan. When multiple factors like environmental fluctuation and hatchery supplementation act simultaneously on a population, interpretation of genetic monitoring data may be equally complex and require considerable ecological data.</p></div>]]></content:encoded><description>The endangered Rio Grande silvery minnow persists as a remnant population in a highly fragmented and regulated arid-land river system. The species is subject to dramatic annual fluctuations in density. Since 2003, the wild population has been supplemented by hatchery-reared fish. We report on a 12-year (1999–2010) monitoring study of genetic diversity and effective population size (Ne) of wild and hatchery stocks. Our goals were to evaluate how genetic metrics responded to changes in wild fish density and whether they corresponded to the number and levels of diversity of hatchery-reared repatriates. Genetic diversity and all measures of Ne in the wild population did not correlate with wild fish density until hatchery supplementation began in earnest. Estimates of variance and inbreeding effective size were not correlated. Our results suggest source–sink dynamics where captive stocks form a genetically diverse source and the wild population behaves as a sink. Nevertheless, overall genetic diversity of silvery minnow has been maintained over the last decade, and we attribute this to a well-designed and executed propagation management plan. When multiple factors like environmental fluctuation and hatchery supplementation act simultaneously on a population, interpretation of genetic monitoring data may be equally complex and require considerable ecological data.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00234.x" xmlns="http://purl.org/rss/1.0/"><title>Toward responsible stock enhancement: broadcast spawning dynamics and adaptive genetic management in white seabass aquaculture</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00234.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Toward responsible stock enhancement: broadcast spawning dynamics and adaptive genetic management in white seabass aquaculture</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kristen M. Gruenthal</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mark A. Drawbridge</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-12T00:24:00.680204-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00234.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.1752-4571.2011.00234.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00234.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The evolutionary effects captive-bred individuals that can have on wild conspecifics are necessary considerations for stock enhancement programs, but breeding protocols are often developed without the knowledge of realized reproductive behavior. To help fill that gap, parentage was assigned to offspring produced by a freely mating group of 50 white seabass (<em>Atractoscion nobilis</em>), a representative broadcast spawning marine finfish cultured for conservation. Similar to the well-known and closely related red drum (<em>Sciaenops ocellatus</em>), <em>A. nobilis</em> exhibited large variation in reproductive success. More males contributed and contributed more equally than females within and among spawns in a mating system best described as lottery polygyny. Two females produced 27% of the seasonal offspring pool and female breeding effective size averaged 1.85 per spawn and 12.38 seasonally, whereas male breeding effective size was higher (6.42 and 20.87, respectively), with every male contributing 1–7% of offspring. Further, females batch spawned every 1–5 weeks, while males displayed continuous reproductive readiness. Sex-specific mating strategies resulted in multiple successful mate pairings and a breeding effective to census size ratio of ≥0.62. Understanding a depleted species’ mating system allowed management to more effectively utilize parental genetic variability for culture, but the fitness consequences of long-term stocking can be difficult to address.</p></div>]]></content:encoded><description>The evolutionary effects captive-bred individuals that can have on wild conspecifics are necessary considerations for stock enhancement programs, but breeding protocols are often developed without the knowledge of realized reproductive behavior. To help fill that gap, parentage was assigned to offspring produced by a freely mating group of 50 white seabass (Atractoscion nobilis), a representative broadcast spawning marine finfish cultured for conservation. Similar to the well-known and closely related red drum (Sciaenops ocellatus), A. nobilis exhibited large variation in reproductive success. More males contributed and contributed more equally than females within and among spawns in a mating system best described as lottery polygyny. Two females produced 27% of the seasonal offspring pool and female breeding effective size averaged 1.85 per spawn and 12.38 seasonally, whereas male breeding effective size was higher (6.42 and 20.87, respectively), with every male contributing 1–7% of offspring. Further, females batch spawned every 1–5 weeks, while males displayed continuous reproductive readiness. Sex-specific mating strategies resulted in multiple successful mate pairings and a breeding effective to census size ratio of ≥0.62. Understanding a depleted species’ mating system allowed management to more effectively utilize parental genetic variability for culture, but the fitness consequences of long-term stocking can be difficult to address.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00231.x" xmlns="http://purl.org/rss/1.0/"><title>Can we understand modern humans without considering pathogens?</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00231.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Can we understand modern humans without considering pathogens?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Frédéric Thomas</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Simon P. Daoust</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michel Raymond</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-09T01:54:51.684937-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00231.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.1752-4571.2011.00231.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00231.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">SYNTHESIS</prism:section><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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Throughout our evolutionary history, humankind has always lived in contact with large numbers of pathogens. Some cultural traits, such as sedentarization and animal domestication, have considerably increased new parasitic contacts and epidemic transitions. Here, we review the various phenotypic traits that have been proposed to be affected by the highly parasitic human environment, including fertility, birth weight, fluctuating asymmetry, body odours, food recipes, sexual behaviour, pregnancy sickness, language, religion and intellectual quotient. We also discuss how such knowledge is important to understanding several aspects of the current problems faced by humanity in our changing world and to predicting the long-term consequences of parasite eradication policies on our health and well-being. The study of the evolutionary interactions between humans and parasites is a burgeoning and most promising field, as demonstrated by the recent increasing popularity of Darwinian medicine.</p></div>]]></content:encoded><description>Throughout our evolutionary history, humankind has always lived in contact with large numbers of pathogens. Some cultural traits, such as sedentarization and animal domestication, have considerably increased new parasitic contacts and epidemic transitions. Here, we review the various phenotypic traits that have been proposed to be affected by the highly parasitic human environment, including fertility, birth weight, fluctuating asymmetry, body odours, food recipes, sexual behaviour, pregnancy sickness, language, religion and intellectual quotient. We also discuss how such knowledge is important to understanding several aspects of the current problems faced by humanity in our changing world and to predicting the long-term consequences of parasite eradication policies on our health and well-being. The study of the evolutionary interactions between humans and parasites is a burgeoning and most promising field, as demonstrated by the recent increasing popularity of Darwinian medicine.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00226.x" xmlns="http://purl.org/rss/1.0/"><title>No recent adaptive selection on the apyrase of Mediterranean Phlebotomus: implications for using salivary peptides to vaccinate against canine leishmaniasis</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00226.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">No recent adaptive selection on the apyrase of Mediterranean Phlebotomus: implications for using salivary peptides to vaccinate against canine leishmaniasis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shazia S. Mahamdallie</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paul D. Ready</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-26T02:17:30.276832-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00226.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.1752-4571.2011.00226.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00226.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Vaccine development is informed by a knowledge of genetic variation among antigen alleles, especially the distribution of positive and balancing selection in populations and species. A combined approach using population genetic and phylogenetic methods to detect selective signatures can therefore be informative for identifying vaccine candidates. Parasitic <em>Leishmania</em> species cause the disease leishmaniasis in humans and mammalian reservoir hosts after inoculation by female phlebotomine sandflies. Like other arthropod vectors of disease agents, sandflies use salivary peptides to counteract host haemostatic and immunomodulatory responses during bloodfeeding, and these peptides are vaccine candidates because they can protect against <em>Leishmania</em> infection. We detected no contemporary adaptive selection on one salivary peptide, apyrase, in 20 populations of <em>Phlebotomus ariasi</em>, a European vector of <em>Leishmania infantum</em>. Maximum likelihood branch models on a gene phylogeny showed apyrase to be a single copy in <em>P. ariasi</em> but an ancient duplication event associated with temporary positive selection was observed in its sister group, which contains most Mediterranean vectors of <em>L. infantum</em>. The absence of contemporary adaptive selection on the apyrase of <em>P. ariasi</em> may result from this sandfly’s opportunistic feeding behaviour. Our study illustrates how the molecular population genetics of arthropods can help investigate the potential of salivary peptides for disease control and for understanding geographical variation in vector competence.</p></div>]]></content:encoded><description>Vaccine development is informed by a knowledge of genetic variation among antigen alleles, especially the distribution of positive and balancing selection in populations and species. A combined approach using population genetic and phylogenetic methods to detect selective signatures can therefore be informative for identifying vaccine candidates. Parasitic Leishmania species cause the disease leishmaniasis in humans and mammalian reservoir hosts after inoculation by female phlebotomine sandflies. Like other arthropod vectors of disease agents, sandflies use salivary peptides to counteract host haemostatic and immunomodulatory responses during bloodfeeding, and these peptides are vaccine candidates because they can protect against Leishmania infection. We detected no contemporary adaptive selection on one salivary peptide, apyrase, in 20 populations of Phlebotomus ariasi, a European vector of Leishmania infantum. Maximum likelihood branch models on a gene phylogeny showed apyrase to be a single copy in P. ariasi but an ancient duplication event associated with temporary positive selection was observed in its sister group, which contains most Mediterranean vectors of L. infantum. The absence of contemporary adaptive selection on the apyrase of P. ariasi may result from this sandfly’s opportunistic feeding behaviour. Our study illustrates how the molecular population genetics of arthropods can help investigate the potential of salivary peptides for disease control and for understanding geographical variation in vector competence.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00227.x" xmlns="http://purl.org/rss/1.0/"><title>The Red Queen and the seed bank: pathogen resistance of ex situ and in situ conserved barley</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00227.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The Red Queen and the seed bank: pathogen resistance of ex situ and in situ conserved barley</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Helen R. Jensen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Antonín Dreiseitl</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mohammed Sadiki</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Daniel J. Schoen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-22T05:57:39.586668-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00227.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.1752-4571.2011.00227.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00227.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Plant geneticists have proposed that the dynamic conservation of crop plants in farm environments (<em>in situ</em> conservation) is complementary to static conservation in seed banks (<em>ex situ</em> conservation) because it may help to ensure adaptation to changing conditions. Here, we test whether collections of a traditional variety of Moroccan barley (<em>Hordeum vulgare</em> ssp. <em>vulgare</em>) conserved <em>ex situ</em> showed differences in qualitative and quantitative resistance to the endemic fungal pathogen, <em>Blumeria graminis</em> f.sp. <em>hordei</em>, compared to collections that were continuously cultivated <em>in situ.</em> In detached-leaf assays for qualitative resistance, there were some significant differences between <em>in situ</em> and <em>ex situ</em> conserved collections from the same localities. Some <em>ex situ</em> conserved collections showed lower resistance levels, while others showed higher resistance levels than their <em>in situ</em> conserved counterparts. In field trials for quantitative resistance, similar results were observed, with the highest resistance observed <em>in situ</em>. Overall, this study identifies some cases where the Red Queen appears to drive the evolution of increased resistance <em>in situ.</em> However, <em>in situ</em> conservation does not always result in improved adaptation to pathogen virulence, suggesting a more complex evolutionary scenario, consistent with several published examples of plant–pathogen co-evolution in wild systems.</p></div>]]></content:encoded><description>Plant geneticists have proposed that the dynamic conservation of crop plants in farm environments (in situ conservation) is complementary to static conservation in seed banks (ex situ conservation) because it may help to ensure adaptation to changing conditions. Here, we test whether collections of a traditional variety of Moroccan barley (Hordeum vulgare ssp. vulgare) conserved ex situ showed differences in qualitative and quantitative resistance to the endemic fungal pathogen, Blumeria graminis f.sp. hordei, compared to collections that were continuously cultivated in situ. In detached-leaf assays for qualitative resistance, there were some significant differences between in situ and ex situ conserved collections from the same localities. Some ex situ conserved collections showed lower resistance levels, while others showed higher resistance levels than their in situ conserved counterparts. In field trials for quantitative resistance, similar results were observed, with the highest resistance observed in situ. Overall, this study identifies some cases where the Red Queen appears to drive the evolution of increased resistance in situ. However, in situ conservation does not always result in improved adaptation to pathogen virulence, suggesting a more complex evolutionary scenario, consistent with several published examples of plant–pathogen co-evolution in wild systems.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00228.x" xmlns="http://purl.org/rss/1.0/"><title>Genetic structure and local adaptation of European wheat yellow rust populations: the role of temperature-specific adaptation</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00228.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genetic structure and local adaptation of European wheat yellow rust populations: the role of temperature-specific adaptation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mamadou Mboup</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bochra Bahri</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marc Leconte</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Claude De Vallavieille-Pope</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Oliver Kaltz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jérôme Enjalbert</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-22T00:39:28.13647-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00228.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.1752-4571.2011.00228.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00228.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Environmental heterogeneity influences coevolution and local adaptation in host–parasite systems. This also concerns applied issues, because the geographic range of parasites may depend on their capacity to adapt to abiotic conditions. We studied temperature-specific adaptation in the wheat yellow/stripe rust pathogen, <em>Puccinia striiformis</em> f.sp. <em>tritici</em> (<em>PST</em>). Using laboratory experiments, <em>PST</em> isolates from northern and southern France were studied for their ability to germinate and to infect bread and durum wheat cultivars over a temperature gradient. Pathogen origin × temperature interactions for infectivity and germination rate suggest local adaptation to high- versus low-temperature regimes in south and north. Competition experiments in southern and northern field sites showed a general competitive advantage of southern over northern isolates. This advantage was particularly pronounced in the southern ‘home’ site, consistent with a model integrating laboratory infectivity and field temperature variation. The stable <em>PST</em> population structure in France likely reflects adaptation to ecological and genetic factors: persistence of southern <em>PST</em> may be due to adaptation to the warmer Mediterranean climate; and persistence of northern <em>PST</em> can be explained by adaptation to commonly used cultivars, for which southern isolates are lacking the relevant virulence genes. Thus, understanding the role of temperature-specific adaptations may help to improve forecast models or breeding programmes.</p></div>]]></content:encoded><description>Environmental heterogeneity influences coevolution and local adaptation in host–parasite systems. This also concerns applied issues, because the geographic range of parasites may depend on their capacity to adapt to abiotic conditions. We studied temperature-specific adaptation in the wheat yellow/stripe rust pathogen, Puccinia striiformis f.sp. tritici (PST). Using laboratory experiments, PST isolates from northern and southern France were studied for their ability to germinate and to infect bread and durum wheat cultivars over a temperature gradient. Pathogen origin × temperature interactions for infectivity and germination rate suggest local adaptation to high- versus low-temperature regimes in south and north. Competition experiments in southern and northern field sites showed a general competitive advantage of southern over northern isolates. This advantage was particularly pronounced in the southern ‘home’ site, consistent with a model integrating laboratory infectivity and field temperature variation. The stable PST population structure in France likely reflects adaptation to ecological and genetic factors: persistence of southern PST may be due to adaptation to the warmer Mediterranean climate; and persistence of northern PST can be explained by adaptation to commonly used cultivars, for which southern isolates are lacking the relevant virulence genes. Thus, understanding the role of temperature-specific adaptations may help to improve forecast models or breeding programmes.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00225.x" xmlns="http://purl.org/rss/1.0/"><title>Genotype × genotype interactions between the toxic cyanobacterium Microcystis and its grazer, the waterflea Daphnia</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00225.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genotype × genotype interactions between the toxic cyanobacterium Microcystis and its grazer, the waterflea Daphnia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Veerle Lemaire</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Silvia Brusciotti</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ineke van Gremberghe</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wim Vyverman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joost Vanoverbeke</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Luc De Meester</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-22T00:39:23.983157-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00225.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.1752-4571.2011.00225.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00225.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Toxic algal blooms are an important problem worldwide. The literature on toxic cyanobacteria blooms in inland waters reports widely divergent results on whether zooplankton can control cyanobacteria blooms or cyanobacteria suppress zooplankton by their toxins. Here we test whether this may be due to genotype × genotype interactions, in which interactions between the large-bodied and efficient grazer <em>Daphnia</em> and the widespread cyanobacterium <em>Microcystis</em> are not only dependent on <em>Microcystis</em> strain or <em>Daphnia</em> genotype but are specific to genotype × genotype combinations. We show that genotype × genotype interactions are important in explaining mortality in short-time exposures of <em>Daphnia</em> to <em>Microcystis</em>. These genotype × genotype interactions may result in local coadaptation and a geographic mosaic of coevolution. Genotype × genotype interactions can explain why the literature on zooplankton–cyanobacteria interactions is seemingly inconsistent, and provide hope that zooplankton can contribute to the suppression of cyanobacteria blooms in restoration projects.</p></div>]]></content:encoded><description>Toxic algal blooms are an important problem worldwide. The literature on toxic cyanobacteria blooms in inland waters reports widely divergent results on whether zooplankton can control cyanobacteria blooms or cyanobacteria suppress zooplankton by their toxins. Here we test whether this may be due to genotype × genotype interactions, in which interactions between the large-bodied and efficient grazer Daphnia and the widespread cyanobacterium Microcystis are not only dependent on Microcystis strain or Daphnia genotype but are specific to genotype × genotype combinations. We show that genotype × genotype interactions are important in explaining mortality in short-time exposures of Daphnia to Microcystis. These genotype × genotype interactions may result in local coadaptation and a geographic mosaic of coevolution. Genotype × genotype interactions can explain why the literature on zooplankton–cyanobacteria interactions is seemingly inconsistent, and provide hope that zooplankton can contribute to the suppression of cyanobacteria blooms in restoration projects.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00230.x" xmlns="http://purl.org/rss/1.0/"><title>Changing organisms in rapidly changing anthropogenic landscapes: the significance of the ‘Umwelt’-concept and functional habitat for animal conservation</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00230.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Changing organisms in rapidly changing anthropogenic landscapes: the significance of the ‘Umwelt’-concept and functional habitat for animal conservation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hans Van Dyck</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-16T08:05:46.165509-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00230.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.1752-4571.2011.00230.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00230.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">PERSPECTIVE</prism:section><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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>There is a growing recognition for the significance of evolutionary thinking in ecology and conservation biology. However, ecology and conservation studies often work with species-specific, fixed traits that ignore intraspecific variation. The way the habitat of a species is considered is an example of typological thinking biased by human perception. Structural habitat units (e.g., land cover types) as perceived by humans may not represent functional habitat units for other organisms. Human activity may also interfere with the environmental information used by organisms. Therefore, the Umwelt-concept from ethology needs to be integrated in the way we think about habitat and habitat selection. It states that different organisms live in different perceptual worlds dealing with specific subsamples of the environment as a result of their evolutionary and developmental history. The resource-based habitat concept is a functional habitat model based on resource distributions (consumables and conditions) and individual movements. This behavioural approach takes into account aspects that relate to the perceptual world of organisms. This approach may offer new opportunities for conservation and may help avoid failures with habitat restoration. Perceptual ability may be subject to adaptive change, but it may also constrain organisms from showing adaptive behaviours in rapidly changing environments.</p></div>]]></content:encoded><description>There is a growing recognition for the significance of evolutionary thinking in ecology and conservation biology. However, ecology and conservation studies often work with species-specific, fixed traits that ignore intraspecific variation. The way the habitat of a species is considered is an example of typological thinking biased by human perception. Structural habitat units (e.g., land cover types) as perceived by humans may not represent functional habitat units for other organisms. Human activity may also interfere with the environmental information used by organisms. Therefore, the Umwelt-concept from ethology needs to be integrated in the way we think about habitat and habitat selection. It states that different organisms live in different perceptual worlds dealing with specific subsamples of the environment as a result of their evolutionary and developmental history. The resource-based habitat concept is a functional habitat model based on resource distributions (consumables and conditions) and individual movements. This behavioural approach takes into account aspects that relate to the perceptual world of organisms. This approach may offer new opportunities for conservation and may help avoid failures with habitat restoration. Perceptual ability may be subject to adaptive change, but it may also constrain organisms from showing adaptive behaviours in rapidly changing environments.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00223.x" xmlns="http://purl.org/rss/1.0/"><title>Gene flow among wild and domesticated almond species: insights from chloroplast and nuclear markers</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00223.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Gene flow among wild and domesticated almond species: insights from chloroplast and nuclear markers</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Malou Delplancke</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nadir Alvarez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anahí Espíndola</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hélène Joly</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laure Benoit</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Elise Brouck</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nils Arrigo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-16T05:21:52.032665-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00223.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.1752-4571.2011.00223.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00223.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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><b>Abstract</b> Hybridization has played a central role in the evolutionary history of domesticated plants. Notably, several breeding programs relying on gene introgression from the wild compartment have been performed in fruit tree species within the genus <em>Prunus</em> but few studies investigated spontaneous gene flow among wild and domesticated <em>Prunus</em> species. Consequently, a comprehensive understanding of genetic relationships and levels of gene flow between domesticated and wild <em>Prunus</em> species is needed. Combining nuclear and chloroplastic microsatellites, we investigated the gene flow and hybridization among two key almond tree species, the cultivated <em>Prunus dulcis</em> and one of the most widespread wild relative <em>Prunus orientalis</em> in the Fertile Crescent. We detected high genetic diversity levels in both species along with substantial and symmetric gene flow between the domesticated <em>P. dulcis</em> and the wild <em>P. orientalis</em>. These results were discussed in light of the cultivated species diversity, by outlining the frequent spontaneous genetic contributions of wild species to the domesticated compartment. In addition, crop-to-wild gene flow suggests that ad hoc transgene containment strategies would be required if genetically modified cultivars were introduced in the northwestern Mediterranean.</p></div>]]></content:encoded><description>Abstract Hybridization has played a central role in the evolutionary history of domesticated plants. Notably, several breeding programs relying on gene introgression from the wild compartment have been performed in fruit tree species within the genus Prunus but few studies investigated spontaneous gene flow among wild and domesticated Prunus species. Consequently, a comprehensive understanding of genetic relationships and levels of gene flow between domesticated and wild Prunus species is needed. Combining nuclear and chloroplastic microsatellites, we investigated the gene flow and hybridization among two key almond tree species, the cultivated Prunus dulcis and one of the most widespread wild relative Prunus orientalis in the Fertile Crescent. We detected high genetic diversity levels in both species along with substantial and symmetric gene flow between the domesticated P. dulcis and the wild P. orientalis. These results were discussed in light of the cultivated species diversity, by outlining the frequent spontaneous genetic contributions of wild species to the domesticated compartment. In addition, crop-to-wild gene flow suggests that ad hoc transgene containment strategies would be required if genetically modified cultivars were introduced in the northwestern Mediterranean.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00218.x" xmlns="http://purl.org/rss/1.0/"><title>Interpopulation variation in allelopathic traits informs restoration of invaded landscapes</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00218.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Interpopulation variation in allelopathic traits informs restoration of invaded landscapes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Richard A. Lankau</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-08T09:54:32.739857-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00218.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.1752-4571.2011.00218.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00218.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Invasive species can show substantial genetic variation in ecologically important traits, across ranges as well within the introduced range. If these traits affect competition with native species, then management may benefit from considering the genetic landscape of the invader. Across their introduced range, <em>Alliaria petiolata</em> populations vary in their investment in allelopathic traits according to invasion history, which could lead to gradients of impact on native species. Red oak (<em>Quercus rubra</em>) seedlings were transplanted into eight <em>A. petiolata</em>-invaded sites that varied in their invasion history and allelochemical concentrations. At each site, an invader removal treatment was crossed with experimental inoculations of native soil biota, to test whether the benefits of these restoration actions differed across invader populations. <em>Q. rubra</em> seedlings grew faster in invader populations with a longer invasion history and lower allelochemical concentrations. Invader removal and soil inoculation interacted to determine seedling growth, with the benefits of soil inoculation increasing in younger and more highly allelopathic invader populations. A greenhouse experiment using soils collected from experimentally inoculated field plots found similar patterns. These results suggest that the impact of this invader varies across landscapes and that knowledge of this variation could improve the efficacy and efficiency of restoration activities.</p></div>]]></content:encoded><description>Invasive species can show substantial genetic variation in ecologically important traits, across ranges as well within the introduced range. If these traits affect competition with native species, then management may benefit from considering the genetic landscape of the invader. Across their introduced range, Alliaria petiolata populations vary in their investment in allelopathic traits according to invasion history, which could lead to gradients of impact on native species. Red oak (Quercus rubra) seedlings were transplanted into eight A. petiolata-invaded sites that varied in their invasion history and allelochemical concentrations. At each site, an invader removal treatment was crossed with experimental inoculations of native soil biota, to test whether the benefits of these restoration actions differed across invader populations. Q. rubra seedlings grew faster in invader populations with a longer invasion history and lower allelochemical concentrations. Invader removal and soil inoculation interacted to determine seedling growth, with the benefits of soil inoculation increasing in younger and more highly allelopathic invader populations. A greenhouse experiment using soils collected from experimentally inoculated field plots found similar patterns. These results suggest that the impact of this invader varies across landscapes and that knowledge of this variation could improve the efficacy and efficiency of restoration activities.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00222.x" xmlns="http://purl.org/rss/1.0/"><title>Adaptive potential of ash (Fraxinus excelsior) populations against the novel emerging pathogen Hymenoscyphus pseudoalbidus</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00222.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Adaptive potential of ash (Fraxinus excelsior) populations against the novel emerging pathogen Hymenoscyphus pseudoalbidus</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Erik Dahl Kjær</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lea Vig McKinney</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lene Rostgaard Nielsen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lars Nørgaard Hansen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jon Kehlet Hansen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-03T02:57:46.716341-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00222.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.1752-4571.2011.00222.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00222.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>An emerging infectious pathogen <em>Hymenoscyphus pseudoalbidus</em> has spread across much of Europe within recent years causing devastating damage on European common ash trees (<em>Fraxinus excelsior</em>) and associated plant communities. The present study demonstrates the presence of additive genetic variation in susceptibility of natural <em>F. excelsior</em> populations to the new invasive disease. We observe high levels of additive variation in the degree of susceptibility with relatively low influence of environmental factors (narrow-sense heritability = 0.37–0.52). Most native trees are found to be highly susceptible, and we estimate that only around 1% has the potential of producing offspring with expected crown damage of &lt;10% under the present disease pressure. The results suggest that the presence of additive genetic diversity in natural <em>F. excelsior</em> populations can confer the species with important ability to recover, but that low resistance within natural European populations is to be expected because of a low frequency of the hypo-sensitive trees. Large effective population sizes will be required to avoid genetic bottlenecks. The role of artificial selection and breeding for protection of the species is discussed based on the findings.</p></div>]]></content:encoded><description>An emerging infectious pathogen Hymenoscyphus pseudoalbidus has spread across much of Europe within recent years causing devastating damage on European common ash trees (Fraxinus excelsior) and associated plant communities. The present study demonstrates the presence of additive genetic variation in susceptibility of natural F. excelsior populations to the new invasive disease. We observe high levels of additive variation in the degree of susceptibility with relatively low influence of environmental factors (narrow-sense heritability = 0.37–0.52). Most native trees are found to be highly susceptible, and we estimate that only around 1% has the potential of producing offspring with expected crown damage of &lt;10% under the present disease pressure. The results suggest that the presence of additive genetic diversity in natural F. excelsior populations can confer the species with important ability to recover, but that low resistance within natural European populations is to be expected because of a low frequency of the hypo-sensitive trees. Large effective population sizes will be required to avoid genetic bottlenecks. The role of artificial selection and breeding for protection of the species is discussed based on the findings.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00220.x" xmlns="http://purl.org/rss/1.0/"><title>Host tracking or cryptic adaptation? Phylogeography of Pediobius saulius (Hymenoptera, Eulophidae), a parasitoid of the highly invasive horse-chestnut leafminer</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00220.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Host tracking or cryptic adaptation? Phylogeography of Pediobius saulius (Hymenoptera, Eulophidae), a parasitoid of the highly invasive horse-chestnut leafminer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Antonio Hernández-López</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rodolphe Rougerie</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sylvie Augustin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David C. Lees</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rumen Tomov</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marc Kenis</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ejup Çota</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Endrit Kullaj</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christer Hansson</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Giselher Grabenweger</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alain Roques</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carlos López-Vaamonde</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-03T02:47:24.028303-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00220.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.1752-4571.2011.00220.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00220.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Classical biological control is often advocated as a tool for managing invasive species. However, accurate evaluations of parasitoid species complexes and assessment of host specificity are impeded by the lack of morphological variation. Here, we study the possibility of host races/species within the eulophid wasp <em>Pediobius saulius</em>, a pupal generalist parasitoid that parasitize the highly invasive horse-chestnut leaf-mining moth <em>Cameraria ohridella</em>. We analysed the population genetic structure, host associations and phylogeographic patterns of <em>P. saulius</em> in Europe using the COI mitochondrial gene. This marker strongly supports a division into at least five highly differentiated parasitoid complexes, within two of which clades with differing degrees of host specialization were found: a Balkan clade that mainly (but not only) attacks <em>C. ohridella</em> and a more generalist European group that attacks many hosts, including <em>C. ohridella</em>. The divergence in COI (up to 7.6%) suggests the existence of cryptic species, although this is neither confirmed by nuclear divergence nor morphology. We do not find evidence of host tracking. The higher parasitism rates observed in the Balkans and the scarcity of the Balkan–<em>Cameraria</em> haplotypes out of the Balkans open the possibility of using these Balkan haplotypes as biological control agents of <em>C. ohridella</em> elsewhere in Europe.</p></div>]]></content:encoded><description>Classical biological control is often advocated as a tool for managing invasive species. However, accurate evaluations of parasitoid species complexes and assessment of host specificity are impeded by the lack of morphological variation. Here, we study the possibility of host races/species within the eulophid wasp Pediobius saulius, a pupal generalist parasitoid that parasitize the highly invasive horse-chestnut leaf-mining moth Cameraria ohridella. We analysed the population genetic structure, host associations and phylogeographic patterns of P. saulius in Europe using the COI mitochondrial gene. This marker strongly supports a division into at least five highly differentiated parasitoid complexes, within two of which clades with differing degrees of host specialization were found: a Balkan clade that mainly (but not only) attacks C. ohridella and a more generalist European group that attacks many hosts, including C. ohridella. The divergence in COI (up to 7.6%) suggests the existence of cryptic species, although this is neither confirmed by nuclear divergence nor morphology. We do not find evidence of host tracking. The higher parasitism rates observed in the Balkans and the scarcity of the Balkan–Cameraria haplotypes out of the Balkans open the possibility of using these Balkan haplotypes as biological control agents of C. ohridella elsewhere in Europe.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00219.x" xmlns="http://purl.org/rss/1.0/"><title>Blocking the evolution of insecticide-resistant malaria vectors with a microsporidian</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00219.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Blocking the evolution of insecticide-resistant malaria vectors with a microsporidian</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jacob C. Koella</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adam Saddler</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Thomas P. S. Karacs</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-30T04:58:40.63786-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00219.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.1752-4571.2011.00219.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00219.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Finding a way to block the evolution insecticide resistance would be a major breakthrough for the control of malaria. We suggest that this may be possible by introducing a stress into mosquito populations that restores the sensitivity of genetically resistant mosquitoes and that decreases their longevity when they are not exposed to insecticide. We use a mathematical model to show that, despite the intense selection pressure imposed by insecticides, moderate levels of stress might tip the evolutionary balance between costs and benefits of resistance toward maintaining sensitivity. Our experimental work with the microsporidian parasite <em>Vavraia culicis</em> infecting two lines of resistant mosquitoes and a sensitive line suggests that it may indeed be possible to stress the mosquitoes in the required way. The mortality of resistant mosquitoes 24 h after exposure to the insecticide was up to 8.8 times higher in infected than in uninfected ones; if mosquitoes were not exposed to the insecticide, resistant mosquitoes infected by the microsporidian lived about half as long as uninfected ones and insecticide-sensitive mosquitoes (with or without the parasite). Our results suggest that biopesticides or other insecticides that interfere with the expression of resistance may help to manage insecticide resistance in programs of malaria control.</p></div>]]></content:encoded><description>Finding a way to block the evolution insecticide resistance would be a major breakthrough for the control of malaria. We suggest that this may be possible by introducing a stress into mosquito populations that restores the sensitivity of genetically resistant mosquitoes and that decreases their longevity when they are not exposed to insecticide. We use a mathematical model to show that, despite the intense selection pressure imposed by insecticides, moderate levels of stress might tip the evolutionary balance between costs and benefits of resistance toward maintaining sensitivity. Our experimental work with the microsporidian parasite Vavraia culicis infecting two lines of resistant mosquitoes and a sensitive line suggests that it may indeed be possible to stress the mosquitoes in the required way. The mortality of resistant mosquitoes 24 h after exposure to the insecticide was up to 8.8 times higher in infected than in uninfected ones; if mosquitoes were not exposed to the insecticide, resistant mosquitoes infected by the microsporidian lived about half as long as uninfected ones and insecticide-sensitive mosquitoes (with or without the parasite). Our results suggest that biopesticides or other insecticides that interfere with the expression of resistance may help to manage insecticide resistance in programs of malaria control.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00221.x" xmlns="http://purl.org/rss/1.0/"><title>Genetic and maternal effects on tail spine and body length in the invasive spiny water flea (Bythotrephes longimanus)</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00221.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genetic and maternal effects on tail spine and body length in the invasive spiny water flea (Bythotrephes longimanus)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrea L. J. Miehls</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Scott D. Peacor</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrew G. McAdam</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-30T04:55:14.213196-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00221.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.1752-4571.2011.00221.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00221.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Interest in the evolution of invasive species has grown in recent years, yet few studies have investigated sources of variation in invasive species traits experiencing natural selection. The spiny water flea, <em>Bythotrephes longimanus</em>, is an invasive zooplankton in the Great Lakes that exhibits seasonal changes in tail spine and body length consistent with natural selection. Evolution of <em>Bythotrephes</em> traits, however, depends on the presence and magnitude of quantitative genetic variation, which could change within or across years. Clonal analysis of wild-captured <em>Bythotrephes</em> indicated that variance components for distal spine length were variable among but not within years. Spine length was always heritable but was not always influenced by maternal effects. In contrast, variance components for body length varied both within and among years, but likewise body length was always heritable and not always influenced by maternal effects. Results indicate that important <em>Bythotrephes</em> traits have heritable variation comparable to native species and other invasive species that would enable an evolutionary response to natural selection. This evolutionary capacity could contribute to the widespread success and dramatic effects of <em>Bythotrephes</em> invasion in systems with diverse biotic and abiotic conditions.</p></div>]]></content:encoded><description>Interest in the evolution of invasive species has grown in recent years, yet few studies have investigated sources of variation in invasive species traits experiencing natural selection. The spiny water flea, Bythotrephes longimanus, is an invasive zooplankton in the Great Lakes that exhibits seasonal changes in tail spine and body length consistent with natural selection. Evolution of Bythotrephes traits, however, depends on the presence and magnitude of quantitative genetic variation, which could change within or across years. Clonal analysis of wild-captured Bythotrephes indicated that variance components for distal spine length were variable among but not within years. Spine length was always heritable but was not always influenced by maternal effects. In contrast, variance components for body length varied both within and among years, but likewise body length was always heritable and not always influenced by maternal effects. Results indicate that important Bythotrephes traits have heritable variation comparable to native species and other invasive species that would enable an evolutionary response to natural selection. This evolutionary capacity could contribute to the widespread success and dramatic effects of Bythotrephes invasion in systems with diverse biotic and abiotic conditions.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00217.x" xmlns="http://purl.org/rss/1.0/"><title>Genomic toolboxes for conservation biologists</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00217.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genomic toolboxes for conservation biologists</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Francesco Angeloni</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Niels Wagemaker</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Philippine Vergeer</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joop Ouborg</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-17T09:09:42.63951-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00217.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.1752-4571.2011.00217.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00217.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Conservation genetics is expanding its research horizon with a genomic approach, by incorporating the modern techniques of next-generation sequencing (NGS). Application of NGS overcomes many limitations of conservation genetics. First, NGS allows for genome-wide screening of markers, which may lead to a more representative estimation of genetic variation within and between populations. Second, NGS allows for distinction between neutral and non-neutral markers. By screening populations on thousands of single nucleotide polymorphism markers, signals of selection can be found for some markers. Variation in these markers will give insight into functional rather than neutral genetic variation. Third, NGS facilitates the study of gene expression. Conservation genomics will increase our insight in how the environment and genes interact to affect phenotype and fitness. In addition, the NGS approach opens a way to study processes such as inbreeding depression and local adaptation mechanistically. Conservation genetics programs are directed to a fundamental understanding of the processes involved in conservation genetics and should preferably be started in species for which large databases on ecology, demography and genetics are available. Here, we describe and illustrate the connection between the application of NGS technologies and the research questions in conservation. The perspectives of conservation genomics programs are also discussed.</p></div>]]></content:encoded><description>Conservation genetics is expanding its research horizon with a genomic approach, by incorporating the modern techniques of next-generation sequencing (NGS). Application of NGS overcomes many limitations of conservation genetics. First, NGS allows for genome-wide screening of markers, which may lead to a more representative estimation of genetic variation within and between populations. Second, NGS allows for distinction between neutral and non-neutral markers. By screening populations on thousands of single nucleotide polymorphism markers, signals of selection can be found for some markers. Variation in these markers will give insight into functional rather than neutral genetic variation. Third, NGS facilitates the study of gene expression. Conservation genomics will increase our insight in how the environment and genes interact to affect phenotype and fitness. In addition, the NGS approach opens a way to study processes such as inbreeding depression and local adaptation mechanistically. Conservation genetics programs are directed to a fundamental understanding of the processes involved in conservation genetics and should preferably be started in species for which large databases on ecology, demography and genetics are available. Here, we describe and illustrate the connection between the application of NGS technologies and the research questions in conservation. The perspectives of conservation genomics programs are also discussed.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00213.x" xmlns="http://purl.org/rss/1.0/"><title>The implications of nongenetic inheritance for evolution in changing environments</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00213.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The implications of nongenetic inheritance for evolution in changing environments</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Russell Bonduriansky</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Angela J. Crean</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Troy Day</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-08T03:18:28.134725-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00213.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.1752-4571.2011.00213.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00213.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">SYNTHESIS</prism:section><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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Nongenetic inheritance is a potentially important but poorly understood factor in population responses to rapid environmental change. Accumulating evidence indicates that nongenetic inheritance influences a diverse array of traits in all organisms and can allow for the transmission of environmentally induced phenotypic changes (‘acquired traits’), as well as spontaneously arising and highly mutable variants. We review models of adaptation to changing environments under the assumption of a broadened model of inheritance that incorporates nongenetic mechanisms of transmission, and survey relevant empirical examples. Theory suggests that nongenetic inheritance can increase the rate of both phenotypic and genetic change and, in some cases, alter the direction of change. Empirical evidence shows that a diversity of phenotypes – spanning a continuum from adaptive to pathological – can be transmitted nongenetically. The presence of nongenetic inheritance therefore complicates our understanding of evolutionary responses to environmental change. We outline a research program encompassing experimental studies that test for transgenerational effects of a range of environmental factors, followed by theoretical and empirical studies on the population-level consequences of such effects.</p></div>]]></content:encoded><description>Nongenetic inheritance is a potentially important but poorly understood factor in population responses to rapid environmental change. Accumulating evidence indicates that nongenetic inheritance influences a diverse array of traits in all organisms and can allow for the transmission of environmentally induced phenotypic changes (‘acquired traits’), as well as spontaneously arising and highly mutable variants. We review models of adaptation to changing environments under the assumption of a broadened model of inheritance that incorporates nongenetic mechanisms of transmission, and survey relevant empirical examples. Theory suggests that nongenetic inheritance can increase the rate of both phenotypic and genetic change and, in some cases, alter the direction of change. Empirical evidence shows that a diversity of phenotypes – spanning a continuum from adaptive to pathological – can be transmitted nongenetically. The presence of nongenetic inheritance therefore complicates our understanding of evolutionary responses to environmental change. We outline a research program encompassing experimental studies that test for transgenerational effects of a range of environmental factors, followed by theoretical and empirical studies on the population-level consequences of such effects.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00216.x" xmlns="http://purl.org/rss/1.0/"><title>Modeling intraspecific adaptation of Abies sachalinensis to local altitude and responses to global warming, based on a 36-year reciprocal transplant experiment</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00216.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Modeling intraspecific adaptation of Abies sachalinensis to local altitude and responses to global warming, based on a 36-year reciprocal transplant experiment</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wataru Ishizuka</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Susumu Goto</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-07T01:00:43.683388-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00216.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.1752-4571.2011.00216.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00216.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Intraspecific adaptation in <em>Abies sachalinensis</em> was examined using models based on long-term monitoring data gathered during a reciprocal transplant experiment with eight seed source populations and six transplantation sites along an altitudinal gradient. The consequence of local adaptation was evaluated by testing the home-site advantage for upslope and downslope transplants at five ages. The populations’ fitness-linked trait was set as their productivity (tree height × survival rate) at each age. The effects of global warming were evaluated on the basis of the 36-year performance of downslope transplants. Evidence was found for adaptive genetic variation affecting both height and survival from an early age. Increasing the distance between seed source and planting site significantly reduced productivity for both upslope and downslope transplantation, demonstrating the existence of a significant home-site advantage. The decrease in productivity was most distinct for upslope transplantations, indicating strong local adaptation to high altitudes. Global warming is predicted to increase the productivity of high-altitude populations. However, owing to their existing local adaptation, all tested populations exhibited lower productivity under warming than demes that were optimal for the new climate. These negative predictions should be considered when planning the management of locally adapted plant species such as <em>A. sachalinensis</em>.</p></div>]]></content:encoded><description>Intraspecific adaptation in Abies sachalinensis was examined using models based on long-term monitoring data gathered during a reciprocal transplant experiment with eight seed source populations and six transplantation sites along an altitudinal gradient. The consequence of local adaptation was evaluated by testing the home-site advantage for upslope and downslope transplants at five ages. The populations’ fitness-linked trait was set as their productivity (tree height × survival rate) at each age. The effects of global warming were evaluated on the basis of the 36-year performance of downslope transplants. Evidence was found for adaptive genetic variation affecting both height and survival from an early age. Increasing the distance between seed source and planting site significantly reduced productivity for both upslope and downslope transplantation, demonstrating the existence of a significant home-site advantage. The decrease in productivity was most distinct for upslope transplantations, indicating strong local adaptation to high altitudes. Global warming is predicted to increase the productivity of high-altitude populations. However, owing to their existing local adaptation, all tested populations exhibited lower productivity under warming than demes that were optimal for the new climate. These negative predictions should be considered when planning the management of locally adapted plant species such as A. sachalinensis.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00215.x" xmlns="http://purl.org/rss/1.0/"><title>Evolutionary and ecological feedbacks of the survival cost of reproduction</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00215.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evolutionary and ecological feedbacks of the survival cost of reproduction</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anna Kuparinen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David C. Hardie</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jeffrey A. Hutchings</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-07T01:00:32.445563-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00215.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.1752-4571.2011.00215.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00215.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Arguably the most fundamental of trade-offs in life-history evolution is the increase in natural mortality resulting from sexual maturity and reproduction. Despite its central importance, this increase in mortality, a survival cost, garners surprisingly little attention in fish and fisheries modeling studies. We undertook an exploratory analysis to evaluate the consequences of this omission for life-history projections. To this end, we developed a simulation approach that integrates quantitative genetics into the ecological dynamics of a fish population and parameterized the model for Atlantic cod (<em>Gadus morhua</em>, L.). When compared to simulations in which the mortality of immature and mature individuals is equal, the inclusion of a survival cost results in larger asymptotic body size, older age at maturity, and larger size at maturity. We also find that measures of population productivity (spawning stock biomass, recruits-per-spawner) are overestimated if the survival cost is excluded. This sensitivity of key metrics of population growth rate and reproductive capacity to the magnitude of the survival cost of reproduction underscores the need to explicitly account for this trade-off in projections of fish population responses to natural and anthropogenic environmental change, including fisheries.</p></div>]]></content:encoded><description>Arguably the most fundamental of trade-offs in life-history evolution is the increase in natural mortality resulting from sexual maturity and reproduction. Despite its central importance, this increase in mortality, a survival cost, garners surprisingly little attention in fish and fisheries modeling studies. We undertook an exploratory analysis to evaluate the consequences of this omission for life-history projections. To this end, we developed a simulation approach that integrates quantitative genetics into the ecological dynamics of a fish population and parameterized the model for Atlantic cod (Gadus morhua, L.). When compared to simulations in which the mortality of immature and mature individuals is equal, the inclusion of a survival cost results in larger asymptotic body size, older age at maturity, and larger size at maturity. We also find that measures of population productivity (spawning stock biomass, recruits-per-spawner) are overestimated if the survival cost is excluded. This sensitivity of key metrics of population growth rate and reproductive capacity to the magnitude of the survival cost of reproduction underscores the need to explicitly account for this trade-off in projections of fish population responses to natural and anthropogenic environmental change, including fisheries.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00214.x" xmlns="http://purl.org/rss/1.0/"><title>Genetic erosion impedes adaptive responses to stressful environments</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00214.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genetic erosion impedes adaptive responses to stressful environments</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Bijlsma</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Volker Loeschcke</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-07T01:00:28.265249-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00214.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.1752-4571.2011.00214.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00214.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">SYNTHESIS</prism:section><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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Biodiversity is increasingly subjected to human-induced changes of the environment. To persist, populations continually have to adapt to these often stressful changes including pollution and climate change. Genetic erosion in small populations, owing to fragmentation of natural habitats, is expected to obstruct such adaptive responses: (i) genetic drift will cause a decrease in the level of adaptive genetic variation, thereby limiting evolutionary responses; (ii) inbreeding and the concomitant inbreeding depression will reduce individual fitness and, consequently, the tolerance of populations to environmental stress. Importantly, inbreeding generally increases the sensitivity of a population to stress, thereby increasing the amount of inbreeding depression. As adaptation to stress is most often accompanied by increased mortality (cost of selection), the increase in the ‘cost of inbreeding’ under stress is expected to severely hamper evolutionary adaptive processes. Inbreeding thus plays a pivotal role in this process and is expected to limit the probability of genetically eroded populations to successfully adapt to stressful environmental conditions. Consequently, the dynamics of small fragmented populations may differ considerably from large nonfragmented populations. The resilience of fragmented populations to changing and deteriorating environments is expected to be greatly decreased. Alleviating inbreeding depression, therefore, is crucial to ensure population persistence.</p></div>]]></content:encoded><description>Biodiversity is increasingly subjected to human-induced changes of the environment. To persist, populations continually have to adapt to these often stressful changes including pollution and climate change. Genetic erosion in small populations, owing to fragmentation of natural habitats, is expected to obstruct such adaptive responses: (i) genetic drift will cause a decrease in the level of adaptive genetic variation, thereby limiting evolutionary responses; (ii) inbreeding and the concomitant inbreeding depression will reduce individual fitness and, consequently, the tolerance of populations to environmental stress. Importantly, inbreeding generally increases the sensitivity of a population to stress, thereby increasing the amount of inbreeding depression. As adaptation to stress is most often accompanied by increased mortality (cost of selection), the increase in the ‘cost of inbreeding’ under stress is expected to severely hamper evolutionary adaptive processes. Inbreeding thus plays a pivotal role in this process and is expected to limit the probability of genetically eroded populations to successfully adapt to stressful environmental conditions. Consequently, the dynamics of small fragmented populations may differ considerably from large nonfragmented populations. The resilience of fragmented populations to changing and deteriorating environments is expected to be greatly decreased. Alleviating inbreeding depression, therefore, is crucial to ensure population persistence.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00212.x" xmlns="http://purl.org/rss/1.0/"><title>Fates beyond traits: ecological consequences of human-induced trait change</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00212.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fates beyond traits: ecological consequences of human-induced trait change</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eric P. Palkovacs</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael T. Kinnison</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cristian Correa</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christopher M. Dalton</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrew P. Hendry</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-28T07:37:37.078766-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00212.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.1752-4571.2011.00212.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00212.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">SYNTHESIS</prism:section><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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Human-induced trait change has been documented in freshwater, marine, and terrestrial ecosystems worldwide. These trait changes are driven by phenotypic plasticity and contemporary evolution. While efforts to manage human-induced trait change are beginning to receive some attention, managing its ecological consequences has received virtually none. Recent work suggests that contemporary trait change can have important effects on the dynamics of populations, communities, and ecosystems. Therefore, trait changes caused by human activity may be shaping ecological dynamics on a global scale. We present evidence for important ecological effects associated with human-induced trait change in a variety of study systems. These effects can occur over large spatial scales and impact system-wide processes such as trophic cascades. Importantly, the magnitude of these effects can be on par with those of traditional ecological drivers such as species presence. However, phenotypic change is not always an agent of ecological change; it can also buffer ecosystems against change. Determining the conditions under which phenotypic change may promote vs prevent ecological change should be a top research priority.</p></div>]]></content:encoded><description>Human-induced trait change has been documented in freshwater, marine, and terrestrial ecosystems worldwide. These trait changes are driven by phenotypic plasticity and contemporary evolution. While efforts to manage human-induced trait change are beginning to receive some attention, managing its ecological consequences has received virtually none. Recent work suggests that contemporary trait change can have important effects on the dynamics of populations, communities, and ecosystems. Therefore, trait changes caused by human activity may be shaping ecological dynamics on a global scale. We present evidence for important ecological effects associated with human-induced trait change in a variety of study systems. These effects can occur over large spatial scales and impact system-wide processes such as trophic cascades. Importantly, the magnitude of these effects can be on par with those of traditional ecological drivers such as species presence. However, phenotypic change is not always an agent of ecological change; it can also buffer ecosystems against change. Determining the conditions under which phenotypic change may promote vs prevent ecological change should be a top research priority.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00208.x" xmlns="http://purl.org/rss/1.0/"><title>A crucial step toward realism: responses to climate change from an evolving metacommunity perspective</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00208.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A crucial step toward realism: responses to climate change from an evolving metacommunity perspective</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mark C. Urban</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Luc De Meester</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mark Vellend</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Robby Stoks</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joost Vanoverbeke</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-07T07:12:34.068204-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00208.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.1752-4571.2011.00208.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00208.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">PERSPECTIVE</prism:section><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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We need to understand joint ecological and evolutionary responses to climate change to predict future threats to biological diversity. The ‘evolving metacommunity’ framework emphasizes that interactions between ecological and evolutionary mechanisms at both local and regional scales will drive community dynamics during climate change. Theory suggests that ecological and evolutionary dynamics often interact to produce outcomes different from those predicted based on either mechanism alone. We highlight two of these dynamics: (i) species interactions prevent adaptation of nonresident species to new niches and (ii) resident species adapt to changing climates and thereby prevent colonization by nonresident species. The rate of environmental change, level of genetic variation, source-sink structure, and dispersal rates mediate between these potential outcomes. Future models should evaluate multiple species, species interactions other than competition, and multiple traits. Future experiments should manipulate factors such as genetic variation and dispersal to determine their joint effects on responses to climate change. Currently, we know much more about how climates will change across the globe than about how species will respond to these changes despite the profound effects these changes will have on global biological diversity. Integrating evolving metacommunity perspectives into climate change biology should produce more accurate predictions about future changes to species distributions and extinction threats.</p></div>]]></content:encoded><description>We need to understand joint ecological and evolutionary responses to climate change to predict future threats to biological diversity. The ‘evolving metacommunity’ framework emphasizes that interactions between ecological and evolutionary mechanisms at both local and regional scales will drive community dynamics during climate change. Theory suggests that ecological and evolutionary dynamics often interact to produce outcomes different from those predicted based on either mechanism alone. We highlight two of these dynamics: (i) species interactions prevent adaptation of nonresident species to new niches and (ii) resident species adapt to changing climates and thereby prevent colonization by nonresident species. The rate of environmental change, level of genetic variation, source-sink structure, and dispersal rates mediate between these potential outcomes. Future models should evaluate multiple species, species interactions other than competition, and multiple traits. Future experiments should manipulate factors such as genetic variation and dispersal to determine their joint effects on responses to climate change. Currently, we know much more about how climates will change across the globe than about how species will respond to these changes despite the profound effects these changes will have on global biological diversity. Integrating evolving metacommunity perspectives into climate change biology should produce more accurate predictions about future changes to species distributions and extinction threats.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00201.x" xmlns="http://purl.org/rss/1.0/"><title>Invasive species as drivers of evolutionary change: cane toads in tropical Australia</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00201.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Invasive species as drivers of evolutionary change: cane toads in tropical Australia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Richard Shine</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-21T23:58:14.218428-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00201.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.1752-4571.2011.00201.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00201.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">SYNTHESIS</prism:section><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[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The arrival of an invasive species can have wide-ranging ecological impacts on native taxa, inducing rapid evolutionary responses in ways that either reduce the invader’s impact or exploit the novel opportunity that it provides. The invasion process itself can cause substantial evolutionary shifts in traits that influence the invader’s dispersal rate (via both adaptive and non-adaptive mechanisms) and its ability to establish new populations. I briefly review the nature of evolutionary changes likely to be set in train by a biological invasion, with special emphasis on recent results from my own research group on the invasion of cane toads (<em>Rhinella marina</em>) through tropical Australia. The toads’ invasion has caused evolutionary changes both in the toads and in native taxa. Many of those changes are adaptive, but others may result from non-adaptive evolutionary processes: for example, the evolved acceleration in toad dispersal rates may be due to spatial sorting of dispersal-enhancing genes, rather than fitness advantages to faster-dispersing individuals. Managers need to incorporate evolutionary dynamics into their conservation planning, because biological invasions can affect both the rates and the trajectories of evolutionary change.</p></div>]]></content:encoded><description>The arrival of an invasive species can have wide-ranging ecological impacts on native taxa, inducing rapid evolutionary responses in ways that either reduce the invader’s impact or exploit the novel opportunity that it provides. The invasion process itself can cause substantial evolutionary shifts in traits that influence the invader’s dispersal rate (via both adaptive and non-adaptive mechanisms) and its ability to establish new populations. I briefly review the nature of evolutionary changes likely to be set in train by a biological invasion, with special emphasis on recent results from my own research group on the invasion of cane toads (Rhinella marina) through tropical Australia. The toads’ invasion has caused evolutionary changes both in the toads and in native taxa. Many of those changes are adaptive, but others may result from non-adaptive evolutionary processes: for example, the evolved acceleration in toad dispersal rates may be due to spatial sorting of dispersal-enhancing genes, rather than fitness advantages to faster-dispersing individuals. Managers need to incorporate evolutionary dynamics into their conservation planning, because biological invasions can affect both the rates and the trajectories of evolutionary change.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00253.x" xmlns="http://purl.org/rss/1.0/"><title>Evolutionary Applications open to all</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00253.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evolutionary Applications open to all</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Louis Bernatchez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michelle Tseng</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2012.00253.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.1752-4571.2012.00253.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2012.00253.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">EDITORIAL</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00202.x" xmlns="http://purl.org/rss/1.0/"><title>Evolution of plant–pollinator mutualisms in response to climate change</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00202.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evolution of plant–pollinator mutualisms in response to climate change</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Tucker Gilman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nicholas S. Fabina</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Karen C. Abbott</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nicole E. Rafferty</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00202.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.1752-4571.2011.00202.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00202.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">2</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">16</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Climate change has the potential to desynchronize the phenologies of interdependent species, with potentially catastrophic effects on mutualist populations. Phenologies can evolve, but the role of evolution in the response of mutualisms to climate change is poorly understood. We developed a model that explicitly considers both the evolution and the population dynamics of a plant–pollinator mutualism under climate change. How the populations evolve, and thus whether the populations and the mutualism persist, depends not only on the rate of climate change but also on the densities and phenologies of other species in the community. Abundant alternative mutualist partners with broad temporal distributions can make a mutualism more robust to climate change, while abundant alternative partners with narrow temporal distributions can make a mutualism less robust. How community composition and the rate of climate change affect the persistence of mutualisms is mediated by two-species Allee thresholds. Understanding these thresholds will help researchers to identify those mutualisms at highest risk owing to climate change.</p></div>]]></content:encoded><description>Climate change has the potential to desynchronize the phenologies of interdependent species, with potentially catastrophic effects on mutualist populations. Phenologies can evolve, but the role of evolution in the response of mutualisms to climate change is poorly understood. We developed a model that explicitly considers both the evolution and the population dynamics of a plant–pollinator mutualism under climate change. How the populations evolve, and thus whether the populations and the mutualism persist, depends not only on the rate of climate change but also on the densities and phenologies of other species in the community. Abundant alternative mutualist partners with broad temporal distributions can make a mutualism more robust to climate change, while abundant alternative partners with narrow temporal distributions can make a mutualism less robust. How community composition and the rate of climate change affect the persistence of mutualisms is mediated by two-species Allee thresholds. Understanding these thresholds will help researchers to identify those mutualisms at highest risk owing to climate change.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00203.x" xmlns="http://purl.org/rss/1.0/"><title>Hybridization and invasion: an experimental test with diffuse knapweed (Centaurea diffusa Lam.)</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00203.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Hybridization and invasion: an experimental test with diffuse knapweed (Centaurea diffusa Lam.)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Amy C. Blair</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dana Blumenthal</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ruth A. Hufbauer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00203.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.1752-4571.2011.00203.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00203.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">17</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">28</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A number of studies have suggested a link between hybridization and invasion. In this study, we experimentally test the potential for hybridization to influence invasion through a greenhouse common garden study. Diffuse knapweed (DK) (<em>Centaurea diffusa</em> Lam.) was introduced to North America with admixture from spotted knapweed (SK) (<em>Centaurea stoebe</em> subsp. <em>stoebe</em> L.). Comparisons between North American DK (including hybrid phenotypes) and native (European) DK in a common garden did not reveal enhanced performance or increased phenotypic variance, suggesting that pre-introduction hybridization or, more generally, post-introduction evolutionary change has not significantly contributed to the invasion of DK. In contrast, early generation hybrids [artificially created Backcross 1 (BC1) plants] exhibited increased variance for eight of the examined traits, and greater leaf and reproductive shoot production when compared to North American DK. Individual BC1 lines differed for several traits, suggesting the importance of the cross for drawing conclusions from such comparisons. When compared to the parental species (DK and SK), the BC1 plants were not transgressive for any of the measured traits. Overall, these findings suggest that if diploid SK is introduced to North America, interspecific hybridization has the potential to result in even more aggressive invaders.</p></div>]]></content:encoded><description>A number of studies have suggested a link between hybridization and invasion. In this study, we experimentally test the potential for hybridization to influence invasion through a greenhouse common garden study. Diffuse knapweed (DK) (Centaurea diffusa Lam.) was introduced to North America with admixture from spotted knapweed (SK) (Centaurea stoebe subsp. stoebe L.). Comparisons between North American DK (including hybrid phenotypes) and native (European) DK in a common garden did not reveal enhanced performance or increased phenotypic variance, suggesting that pre-introduction hybridization or, more generally, post-introduction evolutionary change has not significantly contributed to the invasion of DK. In contrast, early generation hybrids [artificially created Backcross 1 (BC1) plants] exhibited increased variance for eight of the examined traits, and greater leaf and reproductive shoot production when compared to North American DK. Individual BC1 lines differed for several traits, suggesting the importance of the cross for drawing conclusions from such comparisons. When compared to the parental species (DK and SK), the BC1 plants were not transgressive for any of the measured traits. Overall, these findings suggest that if diploid SK is introduced to North America, interspecific hybridization has the potential to result in even more aggressive invaders.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00204.x" xmlns="http://purl.org/rss/1.0/"><title>Interspecific hybridization transfers a previously unknown glyphosate resistance mechanism in Amaranthus species</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00204.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Interspecific hybridization transfers a previously unknown glyphosate resistance mechanism in Amaranthus species</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Todd A. Gaines</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sarah M. Ward</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bekir Bukun</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christopher Preston</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jan E. Leach</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Philip Westra</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00204.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.1752-4571.2011.00204.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00204.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">29</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">38</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A previously unknown glyphosate resistance mechanism, amplification of the 5-enolpyruvyl shikimate-3-phosphate synthase gene, was recently reported in <em>Amaranthus palmeri</em>. This evolved mechanism could introgress to other weedy <em>Amaranthus</em> species through interspecific hybridization, representing an avenue for acquisition of a novel adaptive trait. The objective of this study was to evaluate the potential for this glyphosate resistance trait to transfer via pollen from <em>A. palmeri</em> to five other weedy <em>Amaranthus</em> species (<em>Amaranthus hybridus</em>, <em>Amaranthus powellii</em>, <em>Amaranthus retroflexus</em>, <em>Amaranthus spinosus</em>, and <em>Amaranthus tuberculatus</em>). Field and greenhouse crosses were conducted using glyphosate-resistant male <em>A. palmeri</em> as pollen donors and the other <em>Amaranthus</em> species as pollen recipients. Hybridization between <em>A. palmeri</em> and <em>A. spinosus</em> occurred with frequencies in the field studies ranging from &lt;0.01% to 0.4%, and 1.4% in greenhouse crosses. A majority of the <em>A. spinosus</em> × <em>A. palmeri</em> hybrids grown to flowering were monoecious and produced viable seed. Hybridization occurred in the field study between <em>A. palmeri</em> and <em>A. tuberculatus</em> (&lt;0.2%), and between <em>A. palmeri</em> and <em>A. hybridus</em> (&lt;0.01%). This is the first documentation of hybridization between <em>A. palmeri</em> and both <em>A. spinosus</em> and <em>A. hybridus</em>.</p></div>]]></content:encoded><description>A previously unknown glyphosate resistance mechanism, amplification of the 5-enolpyruvyl shikimate-3-phosphate synthase gene, was recently reported in Amaranthus palmeri. This evolved mechanism could introgress to other weedy Amaranthus species through interspecific hybridization, representing an avenue for acquisition of a novel adaptive trait. The objective of this study was to evaluate the potential for this glyphosate resistance trait to transfer via pollen from A. palmeri to five other weedy Amaranthus species (Amaranthus hybridus, Amaranthus powellii, Amaranthus retroflexus, Amaranthus spinosus, and Amaranthus tuberculatus). Field and greenhouse crosses were conducted using glyphosate-resistant male A. palmeri as pollen donors and the other Amaranthus species as pollen recipients. Hybridization between A. palmeri and A. spinosus occurred with frequencies in the field studies ranging from &lt;0.01% to 0.4%, and 1.4% in greenhouse crosses. A majority of the A. spinosus × A. palmeri hybrids grown to flowering were monoecious and produced viable seed. Hybridization occurred in the field study between A. palmeri and A. tuberculatus (&lt;0.2%), and between A. palmeri and A. hybridus (&lt;0.01%). This is the first documentation of hybridization between A. palmeri and both A. spinosus and A. hybridus.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00206.x" xmlns="http://purl.org/rss/1.0/"><title>Detection of outlier loci and their utility for fisheries management</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00206.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Detection of outlier loci and their utility for fisheries management</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael A. Russello</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stephanie L. Kirk</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Karen K. Frazer</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paul J. Askey</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00206.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.1752-4571.2011.00206.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00206.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">39</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">52</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Genetics-based approaches have informed fisheries management for decades, yet remain challenging to implement within systems involving recently diverged stocks or where gene flow persists. In such cases, genetic markers exhibiting locus-specific (‘outlier’) effects associated with divergent selection may provide promising alternatives to loci that reflect genome-wide (‘neutral’) effects for guiding fisheries management. Okanagan Lake kokanee (<em>Oncorhynchus nerka</em>), a fishery of conservation concern, exhibits two sympatric ecotypes adapted to different reproductive environments; however, previous research demonstrated the limited utility of neutral microsatellites for assigning individuals. Here, we investigated the efficacy of an outlier-based approach to fisheries management by screening &gt;11 000 expressed sequence tags for linked microsatellites and conducting genomic scans for kokanee sampled across seven spawning sites. We identified eight outliers among 52 polymorphic loci that detected ecotype-level divergence, whereas there was no evidence of divergence at neutral loci. Outlier loci exhibited the highest self-assignment accuracy to ecotype (92.1%), substantially outperforming 44 neutral loci (71.8%). Results were robust among-sampling years, with assignment and mixed composition estimates for individuals sampled in 2010 mirroring baseline results. Overall, outlier loci constitute promising alternatives for informing fisheries management involving recently diverged stocks, with potential applications for designating management units across a broad range of taxa.</p></div>]]></content:encoded><description>Genetics-based approaches have informed fisheries management for decades, yet remain challenging to implement within systems involving recently diverged stocks or where gene flow persists. In such cases, genetic markers exhibiting locus-specific (‘outlier’) effects associated with divergent selection may provide promising alternatives to loci that reflect genome-wide (‘neutral’) effects for guiding fisheries management. Okanagan Lake kokanee (Oncorhynchus nerka), a fishery of conservation concern, exhibits two sympatric ecotypes adapted to different reproductive environments; however, previous research demonstrated the limited utility of neutral microsatellites for assigning individuals. Here, we investigated the efficacy of an outlier-based approach to fisheries management by screening &gt;11 000 expressed sequence tags for linked microsatellites and conducting genomic scans for kokanee sampled across seven spawning sites. We identified eight outliers among 52 polymorphic loci that detected ecotype-level divergence, whereas there was no evidence of divergence at neutral loci. Outlier loci exhibited the highest self-assignment accuracy to ecotype (92.1%), substantially outperforming 44 neutral loci (71.8%). Results were robust among-sampling years, with assignment and mixed composition estimates for individuals sampled in 2010 mirroring baseline results. Overall, outlier loci constitute promising alternatives for informing fisheries management involving recently diverged stocks, with potential applications for designating management units across a broad range of taxa.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00207.x" xmlns="http://purl.org/rss/1.0/"><title>Assessing the role of non-cotton refuges in delaying Helicoverpa armigera resistance to Bt cotton in West Africa</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00207.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Assessing the role of non-cotton refuges in delaying Helicoverpa armigera resistance to Bt cotton in West Africa</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Thierry Brévault</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Samuel Nibouche</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joseph Achaleke</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yves Carrière</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00207.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.1752-4571.2011.00207.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00207.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">53</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">65</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Non-cotton host plants without <em>Bacillus thuringiensis</em> (Bt) toxins can provide refuges that delay resistance to Bt cotton in polyphagous insect pests. It has proven difficult, however, to determine the effective contribution of such refuges and their role in delaying resistance evolution. Here, we used biogeochemical markers to quantify movement of <em>Helicoverpa armigera</em> moths from non-cotton hosts to cotton fields in three agricultural landscapes of the West African cotton belt (Cameroon) where Bt cotton was absent. We show that the contribution of non-cotton hosts as a source of moths was spatially and temporally variable, but at least equivalent to a 7.5% sprayed refuge of non-Bt cotton. Simulation models incorporating <em>H. armigera</em> biological parameters, however, indicate that planting non-Bt cotton refuges may be needed to significantly delay resistance to cotton producing the toxins Cry1Ac and Cry2Ab. Specifically, when the concentration of one toxin (here Cry1Ac) declined seasonally, resistance to Bt cotton often occurred rapidly in simulations where refuges of non-Bt cotton were rare and resistance to Cry2Ab was non-recessive, because resistance was essentially driven by one toxin (here Cry2Ab). The use of biogeochemical markers to quantify insect movement can provide a valuable tool to evaluate the role of non-cotton refuges in delaying the evolution of <em>H. armigera</em> resistance to Bt cotton.</p></div>]]></content:encoded><description>Non-cotton host plants without Bacillus thuringiensis (Bt) toxins can provide refuges that delay resistance to Bt cotton in polyphagous insect pests. It has proven difficult, however, to determine the effective contribution of such refuges and their role in delaying resistance evolution. Here, we used biogeochemical markers to quantify movement of Helicoverpa armigera moths from non-cotton hosts to cotton fields in three agricultural landscapes of the West African cotton belt (Cameroon) where Bt cotton was absent. We show that the contribution of non-cotton hosts as a source of moths was spatially and temporally variable, but at least equivalent to a 7.5% sprayed refuge of non-Bt cotton. Simulation models incorporating H. armigera biological parameters, however, indicate that planting non-Bt cotton refuges may be needed to significantly delay resistance to cotton producing the toxins Cry1Ac and Cry2Ab. Specifically, when the concentration of one toxin (here Cry1Ac) declined seasonally, resistance to Bt cotton often occurred rapidly in simulations where refuges of non-Bt cotton were rare and resistance to Cry2Ab was non-recessive, because resistance was essentially driven by one toxin (here Cry2Ab). The use of biogeochemical markers to quantify insect movement can provide a valuable tool to evaluate the role of non-cotton refuges in delaying the evolution of H. armigera resistance to Bt cotton.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00209.x" xmlns="http://purl.org/rss/1.0/"><title>Development on drought-stressed host plants affects life history, flight morphology and reproductive output relative to landscape structure</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00209.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Development on drought-stressed host plants affects life history, flight morphology and reproductive output relative to landscape structure</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Melanie Gibbs</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hans Van Dyck</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Casper J. Breuker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00209.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.1752-4571.2011.00209.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00209.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">66</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">75</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>With global climate change, rainfall is becoming more variable. Predicting the responses of species to changing rainfall levels is difficult because, for example in herbivorous species, these effects may be mediated indirectly through changes in host plant quality. Furthermore, species responses may result from a simultaneous interaction between rainfall levels and other environmental variables such as anthropogenic land use or habitat quality. In this eco-evolutionary study, we examined how male and female <em>Pararge aegeria</em> (L.) from woodland and agricultural landscape populations were affected by the development on drought-stressed host plants. Compared with individuals from woodland landscapes, when reared on drought-stressed plants agricultural individuals had longer development times, reduced survival rates and lower adult body masses. Across both landscape types, growth on drought-stressed plants resulted in males and females with low forewing aspect ratios and in females with lower wing loading and reduced fecundity. Development on drought-stressed plants also had a landscape-specific effect on reproductive output; agricultural females laid eggs that had a significantly lower hatching success. Overall, our results highlight several potential mechanisms by which low water availability, via changes in host plant quality, may differentially influence <em>P. aegeria</em> populations relative to landscape structure.</p></div>]]></content:encoded><description>With global climate change, rainfall is becoming more variable. Predicting the responses of species to changing rainfall levels is difficult because, for example in herbivorous species, these effects may be mediated indirectly through changes in host plant quality. Furthermore, species responses may result from a simultaneous interaction between rainfall levels and other environmental variables such as anthropogenic land use or habitat quality. In this eco-evolutionary study, we examined how male and female Pararge aegeria (L.) from woodland and agricultural landscape populations were affected by the development on drought-stressed host plants. Compared with individuals from woodland landscapes, when reared on drought-stressed plants agricultural individuals had longer development times, reduced survival rates and lower adult body masses. Across both landscape types, growth on drought-stressed plants resulted in males and females with low forewing aspect ratios and in females with lower wing loading and reduced fecundity. Development on drought-stressed plants also had a landscape-specific effect on reproductive output; agricultural females laid eggs that had a significantly lower hatching success. Overall, our results highlight several potential mechanisms by which low water availability, via changes in host plant quality, may differentially influence P. aegeria populations relative to landscape structure.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00210.x" xmlns="http://purl.org/rss/1.0/"><title>Introgression of domesticated alleles into a wild trout genotype and the impact on seasonal survival in natural lakes</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00210.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Introgression of domesticated alleles into a wild trout genotype and the impact on seasonal survival in natural lakes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wendy Vandersteen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pete Biro</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Les Harris</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Robert Devlin</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00210.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.1752-4571.2011.00210.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00210.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ORIGINAL ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">76</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">88</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We tested the fitness consequences of introgression of fast-growing domesticated fish into a wild population. Fry from wild and domesticated rainbow trout (<em>Oncorhynchus mykiss</em>) crosses, F<sub>1</sub> hybrids, and first- and second-generation backcrosses were released into two natural lakes. Parentage analysis using microsatellite loci facilitated the identification of survivors, so fitness was estimated in nature from the first-feeding stage. Results indicated that under certain conditions, domesticated fish survived at least as well as wild fish within the same environment. Relative growth and survival of the crosses, however, were highly dependent on environment. During the first summer, fastest-growing crosses had the highest survival, but this trend was reversed after one winter and another summer. Although the F<sub>1</sub> hybrids showed evidence of outbreeding depression because of the disruption of local adaptation, there was little evidence of outbreeding depression in the backcrosses, and the second-generation backcrosses exhibited a wild-type phenotype. This information is relevant for assessing the multigenerational risk of escaped or released domesticated fish should they successfully interbreed with wild populations and provides information on how to minimize detrimental impacts of a conservation breeding and/or management programme. These data also further understanding of the selection pressures in nature that maintain submaximal rates of growth.</p></div>]]></content:encoded><description>We tested the fitness consequences of introgression of fast-growing domesticated fish into a wild population. Fry from wild and domesticated rainbow trout (Oncorhynchus mykiss) crosses, F1 hybrids, and first- and second-generation backcrosses were released into two natural lakes. Parentage analysis using microsatellite loci facilitated the identification of survivors, so fitness was estimated in nature from the first-feeding stage. Results indicated that under certain conditions, domesticated fish survived at least as well as wild fish within the same environment. Relative growth and survival of the crosses, however, were highly dependent on environment. During the first summer, fastest-growing crosses had the highest survival, but this trend was reversed after one winter and another summer. Although the F1 hybrids showed evidence of outbreeding depression because of the disruption of local adaptation, there was little evidence of outbreeding depression in the backcrosses, and the second-generation backcrosses exhibited a wild-type phenotype. This information is relevant for assessing the multigenerational risk of escaped or released domesticated fish should they successfully interbreed with wild populations and provides information on how to minimize detrimental impacts of a conservation breeding and/or management programme. These data also further understanding of the selection pressures in nature that maintain submaximal rates of growth.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00211.x" xmlns="http://purl.org/rss/1.0/"><title>Anthropogenically induced adaptation to invade (AIAI): contemporary adaptation to human-altered habitats within the native range can promote invasions</title><link>http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00211.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Anthropogenically induced adaptation to invade (AIAI): contemporary adaptation to human-altered habitats within the native range can promote invasions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ruth A. Hufbauer</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Benoît Facon</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Virginie Ravigné</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Julie Turgeon</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Julien Foucaud</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carol E. Lee</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Olivier Rey</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Arnaud Estoup</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1752-4571.2011.00211.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.1752-4571.2011.00211.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1752-4571.2011.00211.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">PERSPECTIVE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">89</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">101</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Adaptive evolution is currently accepted as playing a significant role in biological invasions. Adaptations relevant to invasions are typically thought to occur either recently within the introduced range, as an evolutionary response to novel selection regimes, or within the native range, because of long-term adaptation to the local environment. We propose that recent adaptation within the native range, in particular adaptations to human-altered habitat, could also contribute to the evolution of invasive populations. Populations adapted to human-altered habitats in the native range are likely to increase in abundance within areas frequented by humans and associated with human transport mechanisms, thus enhancing the likelihood of transport to a novel range. Given that habitats are altered by humans in similar ways worldwide, as evidenced by global environmental homogenization, propagules from populations adapted to human-altered habitats in the native range should perform well within similarly human-altered habitats in the novel range. We label this scenario ‘Anthropogenically Induced Adaptation to Invade’. We illustrate how it differs from other evolutionary processes that may occur during invasions, and how it can help explain accelerating rates of invasions.</p></div>]]></content:encoded><description>Adaptive evolution is currently accepted as playing a significant role in biological invasions. Adaptations relevant to invasions are typically thought to occur either recently within the introduced range, as an evolutionary response to novel selection regimes, or within the native range, because of long-term adaptation to the local environment. We propose that recent adaptation within the native range, in particular adaptations to human-altered habitat, could also contribute to the evolution of invasive populations. Populations adapted to human-altered habitats in the native range are likely to increase in abundance within areas frequented by humans and associated with human transport mechanisms, thus enhancing the likelihood of transport to a novel range. Given that habitats are altered by humans in similar ways worldwide, as evidenced by global environmental homogenization, propagules from populations adapted to human-altered habitats in the native range should perform well within similarly human-altered habitats in the novel range. We label this scenario ‘Anthropogenically Induced Adaptation to Invade’. We illustrate how it differs from other evolutionary processes that may occur during invasions, and how it can help explain accelerating rates of invasions.</description></item></rdf:RDF>
