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       <title>Volume 26, Number 2, April 2016 - British Herpetological Society</title>
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           <title>Volume 26, Number 2, April 2016 - British Herpetological Society</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016?format=html</link>
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           <title>Front Cover</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/860-front-cover-2?format=html</link>
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           <media:title type="plain">Front Cover</media:title>
           <media:description type="html"><![CDATA[<p>&nbsp;</p>]]></media:description>
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           <description><![CDATA[<p>&nbsp;</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>01. Nest attendance influences the diet of nesting female spectacled caiman ([i]Caiman crocodilus[/i]) in Central Amazonia, Brazil</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/861-01-nest-attendance-influences-the-diet-of-nesting-female-spectacled-caiman-i-caiman-crocodilus-i-in-central-amazonia-brazil?format=html</link>
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           <media:title type="plain">01. Nest attendance influences the diet of nesting female spectacled caiman ([i]Caiman crocodilus[/i]) in Central Amazonia, Brazil</media:title>
           <media:description type="html"><![CDATA[<p>﻿pp. 65- 71</p><p><em>Authors: </em>﻿José António Lemos Barão-Nóbrega, Boris Marioni, Diogo Dutra-Araújo, Robinson Botero-Arias, António J.A. Nogueira, William E. Magnusson & Ronis Da Silveira</p>
<p><strong>﻿Abstract</strong>﻿<strong>﻿:</strong>﻿ Although nesting ecology is well studied in crocodilians, there is little information on the diet and feeding habits of nesting females. During the annual dry season (November–December) of 2012, we studied the diet of female spectacled caiman (<em>Caiman crocodilus</em>) attending nests (<em>n</em>=33) and far from nests (<em>n</em>=16) in Piagaçu-Purus Sustainable Development Reserve (PPSDR), Central Amazonia, Brazil. The proportion of empty stomachs in nest-attending females was larger, and the occurrence of fresh food items was lower when compared to females not attending nests. Fish was the most frequent prey item for non-nesting females, while terrestrial invertebrates and snail operculae were the prey items most commonly recovered from stomachs of nesting females. Our study demonstrates that, despite enduring periods of food deprivation associated with nest attendance, nesting females of <em>C. crocodilus</em> still consume nearby available prey, possibly leaving their nest temporarily unattended.</p>
<p><strong>Key words: </strong>Amazonia, diet, feeding, nest, parental care, spectacled caiman</p>]]></media:description>
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           <description><![CDATA[<p>﻿pp. 65- 71</p><p><em>Authors: </em>﻿José António Lemos Barão-Nóbrega, Boris Marioni, Diogo Dutra-Araújo, Robinson Botero-Arias, António J.A. Nogueira, William E. Magnusson & Ronis Da Silveira</p>
<p><strong>﻿Abstract</strong>﻿<strong>﻿:</strong>﻿ Although nesting ecology is well studied in crocodilians, there is little information on the diet and feeding habits of nesting females. During the annual dry season (November–December) of 2012, we studied the diet of female spectacled caiman (<em>Caiman crocodilus</em>) attending nests (<em>n</em>=33) and far from nests (<em>n</em>=16) in Piagaçu-Purus Sustainable Development Reserve (PPSDR), Central Amazonia, Brazil. The proportion of empty stomachs in nest-attending females was larger, and the occurrence of fresh food items was lower when compared to females not attending nests. Fish was the most frequent prey item for non-nesting females, while terrestrial invertebrates and snail operculae were the prey items most commonly recovered from stomachs of nesting females. Our study demonstrates that, despite enduring periods of food deprivation associated with nest attendance, nesting females of <em>C. crocodilus</em> still consume nearby available prey, possibly leaving their nest temporarily unattended.</p>
<p><strong>Key words: </strong>Amazonia, diet, feeding, nest, parental care, spectacled caiman</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>02. Effects of habitat and fragmented-landscape parameters on amphibian distribution at a large spatial scale</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/862-02-effects-of-habitat-and-fragmented-landscape-parameters-on-amphibian-distribution-at-a-large-spatial-scale?format=html</link>
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           <media:title type="plain">02. Effects of habitat and fragmented-landscape parameters on amphibian distribution at a large spatial scale</media:title>
           <media:description type="html"><![CDATA[<p>pp. 73-84</p><p><em>Authors</em>﻿: Audrey Trochet, Jérémy Dechartre, Hugo Le Chevalier, Boris Baillat, Olivier Calvez, Simon Blanchet & Alexandre Ribéron</p>
<p><strong>﻿Abstract: </strong>Amphibians generally have low dispersal abilities and are often habitat specialised, which makes them particularly sensitive to landscape changes, such as habitat destruction and fragmentation. Because they depend on wetlands for breeding, many conservation studies focus on aquatic habitat degradation and destruction. Additionally, few studies showed that changes in terrestrial habitats could be another threat that may cause the decline of amphibian populations. However, little is known about the terrestrial habitat preferences of most species. Although the proximity of forests and wetlands was expected to be positively related to amphibian presence, while human-modified habitats were expected to be avoided by these species, we still have little information on how these responses are species-specific. Based on an ecological niche factor analysis completed by partial least squares path modelling, we tested whether or not relationships between terrestrial and aquatic habitat parameters and occurrences are congruent across a metacommunity of seven amphibian species co-occurring at the regional spatial scale. We highlight that habitat type could strongly affect amphibian presence at large spatial scales, but in different ways. Agricultural landscapes, semi-natural areas and fragmented-landscape parameters showed expected negative correlations with the presence of some species. However, these habitats were also positively associated to the presence of other species. Indeed, because they could offer some benefits, some species could show a preference for these landscapes. Our results should have implications in conservation programmes, and could help predict future distribution and responses of these species to global change, which could be different among species.</p>
<p><strong>﻿Key words: </strong>﻿agricultural landscapes, amphibian presence, ecological niche factor analysis, habitat preference, landscape parameters, partial least squares path modeling</p>
<p>﻿</p>]]></media:description>
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           <description><![CDATA[<p>pp. 73-84</p><p><em>Authors</em>﻿: Audrey Trochet, Jérémy Dechartre, Hugo Le Chevalier, Boris Baillat, Olivier Calvez, Simon Blanchet & Alexandre Ribéron</p>
<p><strong>﻿Abstract: </strong>Amphibians generally have low dispersal abilities and are often habitat specialised, which makes them particularly sensitive to landscape changes, such as habitat destruction and fragmentation. Because they depend on wetlands for breeding, many conservation studies focus on aquatic habitat degradation and destruction. Additionally, few studies showed that changes in terrestrial habitats could be another threat that may cause the decline of amphibian populations. However, little is known about the terrestrial habitat preferences of most species. Although the proximity of forests and wetlands was expected to be positively related to amphibian presence, while human-modified habitats were expected to be avoided by these species, we still have little information on how these responses are species-specific. Based on an ecological niche factor analysis completed by partial least squares path modelling, we tested whether or not relationships between terrestrial and aquatic habitat parameters and occurrences are congruent across a metacommunity of seven amphibian species co-occurring at the regional spatial scale. We highlight that habitat type could strongly affect amphibian presence at large spatial scales, but in different ways. Agricultural landscapes, semi-natural areas and fragmented-landscape parameters showed expected negative correlations with the presence of some species. However, these habitats were also positively associated to the presence of other species. Indeed, because they could offer some benefits, some species could show a preference for these landscapes. Our results should have implications in conservation programmes, and could help predict future distribution and responses of these species to global change, which could be different among species.</p>
<p><strong>﻿Key words: </strong>﻿agricultural landscapes, amphibian presence, ecological niche factor analysis, habitat preference, landscape parameters, partial least squares path modeling</p>
<p>﻿</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
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           <title>02. Appendix</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/863-02-appendix?format=html</link>
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           <media:title type="plain">02. Appendix</media:title>
           <media:description type="html"><![CDATA[<p>Online appendix for 02.&#160;Effects of habitat and fragmented-landscape parameters on amphibian distribution at a large spatial scale.</p>]]></media:description>
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           <description><![CDATA[<p>Online appendix for 02.&#160;Effects of habitat and fragmented-landscape parameters on amphibian distribution at a large spatial scale.</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>03. Quantitative analysis of courtship and mating behaviours in the big-headed turtle, [i]Platysternon megacephalum[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/864-03-quantitative-analysis-of-courtship-and-mating-behaviours-in-the-big-headed-turtle-i-platysternon-megacephalum-i?format=html</link>
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                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/864-03-quantitative-analysis-of-courtship-and-mating-behaviours-in-the-big-headed-turtle-i-platysternon-megacephalum-i/file"
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           <media:title type="plain">03. Quantitative analysis of courtship and mating behaviours in the big-headed turtle, [i]Platysternon megacephalum[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp. 85-91</p><p>&#65279;&#65279;<em>Authors</em>:&#160;&#65279;Yufeng Wei, Shiping Gong, Haitao Shi &amp; Weiye Li</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;Turtles are an excellent group for understanding the theory of sexual selection, sexual dimorphism and the evolution of courtship behaviour. Asia has a rich diversity of turtle species, but quantitative analysis of courtship behaviour has only been conducted on a single species. This study quantitatively analysed courtship and mating behaviours of captive <em>Platysternon megacephalum</em> to serve as a basis for future comparisons with other freshwater turtles. A total of 259 courtship behaviour sequences stemming from 66 pairings between 12 males and 24 females were analysed. Seven (approaching, sniffing, chasing, resting, mounting, subduing female, copulating) and three mutually exclusive motor patterns (fleeing, mating resistance, mating acceptance) were performed by males and females, respectively. The temporal sequences of courtship and mating behaviours were analysed using Chi-square tests and Kappa analyses, from which a flow diagram was constructed. Male courtship display patterns involved tactile, visual and olfactory cues for conspecific and sexual recognition. In response, females may have emitted olfactory cues regarding their sex and reproductive status. Male <em>P. megacephalum</em> exhibited biting, but no head movement or foreclaw display in courtship, which differs from other freshwater turtles. This study provides the first record of male biting during courtship behaviour in an Asian turtle species. Recommendations for captive breeding of the endangered species <em>P. megacephalum</em> are presented.</p>
<p><strong>&#65279;Key words</strong>&#65279;<strong>&#65279;:&#160;</strong>&#65279;Asia, behavioural sequences, biting, cinematographic techniques, kappa analysis, Platysternidae</p>]]></media:description>
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           <description><![CDATA[<p>pp. 85-91</p><p>&#65279;&#65279;<em>Authors</em>:&#160;&#65279;Yufeng Wei, Shiping Gong, Haitao Shi &amp; Weiye Li</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;Turtles are an excellent group for understanding the theory of sexual selection, sexual dimorphism and the evolution of courtship behaviour. Asia has a rich diversity of turtle species, but quantitative analysis of courtship behaviour has only been conducted on a single species. This study quantitatively analysed courtship and mating behaviours of captive <em>Platysternon megacephalum</em> to serve as a basis for future comparisons with other freshwater turtles. A total of 259 courtship behaviour sequences stemming from 66 pairings between 12 males and 24 females were analysed. Seven (approaching, sniffing, chasing, resting, mounting, subduing female, copulating) and three mutually exclusive motor patterns (fleeing, mating resistance, mating acceptance) were performed by males and females, respectively. The temporal sequences of courtship and mating behaviours were analysed using Chi-square tests and Kappa analyses, from which a flow diagram was constructed. Male courtship display patterns involved tactile, visual and olfactory cues for conspecific and sexual recognition. In response, females may have emitted olfactory cues regarding their sex and reproductive status. Male <em>P. megacephalum</em> exhibited biting, but no head movement or foreclaw display in courtship, which differs from other freshwater turtles. This study provides the first record of male biting during courtship behaviour in an Asian turtle species. Recommendations for captive breeding of the endangered species <em>P. megacephalum</em> are presented.</p>
<p><strong>&#65279;Key words</strong>&#65279;<strong>&#65279;:&#160;</strong>&#65279;Asia, behavioural sequences, biting, cinematographic techniques, kappa analysis, Platysternidae</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
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           <title>04. Fisheries impact on breeding of olive ridley turtles ([i]Lepidochelys olivacea[/i]) along the Gahirmatha coast, Bay of Bengal, Odisha, India</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/865-04-fisheries-impact-on-breeding-of-olive-ridley-turtles-i-lepidochelys-olivacea-i-along-the-gahirmatha-coast-bay-of-bengal-odisha-india?format=html</link>
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           <media:title type="plain">04. Fisheries impact on breeding of olive ridley turtles ([i]Lepidochelys olivacea[/i]) along the Gahirmatha coast, Bay of Bengal, Odisha, India</media:title>
           <media:description type="html"><![CDATA[<p>pp. 93-98&#160;</p><p><em>&#65279;Authors</em>&#65279;<em>&#65279;:</em>&#65279;&#160;Satyaranjan Behera1, Basudev Tripathy, K. Sivakumar, Binod C. Choudhury<br />&amp; Bivash Pandav</p>
<p><strong>&#65279;Abstract:</strong>&#65279;&#160;In India, the Gahirmatha coast is among the most important nesting grounds of olive ridley turtles, <em>Lepidochelys olivacea</em>. The coastal waters of Odisha are also subjected to heavy commercial fishing activities, leading to turtle-fisheries conflicts. This study was carried out to quantify the effects of fishing on breeding turtles. Data on stranded, dead turtles were collected during three breeding seasons (2007&#8211;08, 2008&#8211;09 and 2009&#8211;10) between November and April along a 35 km stretch. A total of 13,443 dead olive ridleys were counted (2008&#8211;09: n=9502, 2007&#8211;08: n=2754, 2009&#8211;10: n=1187). Maximum mortality occurred in February. Few strandings of dead male turtles were recorded. Stranded turtles had a curved carapace length between 51.3 and 77 cm. Mortality is largely attributed to drowning in trawl nets and caused by gill nets. A decrease in size of adults may be related to their high mortality.</p>
<p><strong>&#65279;Key words:&#160;</strong>&#65279;breeding, fishing, mortality, <em>Lepidochelys olivacea</em>, olive ridley, size class</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/865-04-fisheries-impact-on-breeding-of-olive-ridley-turtles-i-lepidochelys-olivacea-i-along-the-gahirmatha-coast-bay-of-bengal-odisha-india?format=html</guid>
           <description><![CDATA[<p>pp. 93-98&#160;</p><p><em>&#65279;Authors</em>&#65279;<em>&#65279;:</em>&#65279;&#160;Satyaranjan Behera1, Basudev Tripathy, K. Sivakumar, Binod C. Choudhury<br />&amp; Bivash Pandav</p>
<p><strong>&#65279;Abstract:</strong>&#65279;&#160;In India, the Gahirmatha coast is among the most important nesting grounds of olive ridley turtles, <em>Lepidochelys olivacea</em>. The coastal waters of Odisha are also subjected to heavy commercial fishing activities, leading to turtle-fisheries conflicts. This study was carried out to quantify the effects of fishing on breeding turtles. Data on stranded, dead turtles were collected during three breeding seasons (2007&#8211;08, 2008&#8211;09 and 2009&#8211;10) between November and April along a 35 km stretch. A total of 13,443 dead olive ridleys were counted (2008&#8211;09: n=9502, 2007&#8211;08: n=2754, 2009&#8211;10: n=1187). Maximum mortality occurred in February. Few strandings of dead male turtles were recorded. Stranded turtles had a curved carapace length between 51.3 and 77 cm. Mortality is largely attributed to drowning in trawl nets and caused by gill nets. A decrease in size of adults may be related to their high mortality.</p>
<p><strong>&#65279;Key words:&#160;</strong>&#65279;breeding, fishing, mortality, <em>Lepidochelys olivacea</em>, olive ridley, size class</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>05. Species assignment in the [i]Pelophylax ridibundus[/i] x [i]P. perezi[/i] hybridogenetic complex based on 16 newly characterised microsatellite markers</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/866-05-species-assignment-in-the-i-pelophylax-ridibundus-i-x-i-p-perezi-i-hybridogenetic-complex-based-on-16-newly-characterised-microsatellite-markers?format=html</link>
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           <media:title type="plain">05. Species assignment in the [i]Pelophylax ridibundus[/i] x [i]P. perezi[/i] hybridogenetic complex based on 16 newly characterised microsatellite markers</media:title>
           <media:description type="html"><![CDATA[<p>pp. 99-108</p><p><em>&#65279;Authors:&#160;</em>&#65279;Gregorio S&#225;nchez-Montes, Ernesto Recuero, Jorge Guti&#233;rrez-Rodr&#237;guez,&#160;Ivan Gomez-Mestre &amp; I&#241;igo Mart&#237;nez-Solano</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;<em>Pelophylax perezi</em> is an Iberian green waterfrog with high tolerance to habitat alteration that at times shows local population growth and demographic expansion, even where other species decline. However, pond destruction, invasive predators and hybridisation with other European waterfrog species (<em>P. ridibundus</em>) threaten many of its populations across its range. Hybrids of <em>P. perezi</em> and <em>P. ridibundus</em> (<em>P. kl. grafi</em>) can breed successfully with the former parental species after discarding the whole <em>P. perezi</em> genome in the germinal line, thus representing a sexual parasite for <em>P. perez</em>i. However, little is known about the extent of the contact zone of this hybridogenetic complex. Due to the morphological similarity of the three taxa, molecular tools are needed to delineate their respective ranges. Here we characterise a set of 16 microsatellite markers specifically developed for <em>P. perezi</em>. These markers showed moderate to high polymorphism (2&#8211;17 alleles/locus) in two populations from central Spain (<em>n</em>=20 and <em>n</em>=23), allowing individual identification of frogs. Seven of these markers cross-amplified in individuals of P. ridibundus from southern France (3&#8211;8 alleles/locus). These markers were used to genotype samples along a transect from southern France to eastern Spain, encompassing both pure and hybrid individuals. Sample assignment to each taxon was based on the new microsatellite loci and compared with nuclear and mitochondrial sequence data. Our results show that these markers are useful to distinguish <em>P. ridibundus</em>, <em>P. perezi</em> and the hybrid form <em>P. kl. grafi</em> from each other, even when sample sizes are low. The newly characterised markers will also be useful in demographic and phylogeographic studies in <em>P. perezi</em> and are thus a valuable tool for evolutionary and conservation oriented research.</p>
<p><strong>&#65279;Key words:&#160;</strong>&#65279;cross-amplification, hybridisation, microsatellites, <em>Pelophylax kl. grafi</em>, <em>Pelophylax perezi,</em> <em>Pelophylax ridibundus</em></p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/866-05-species-assignment-in-the-i-pelophylax-ridibundus-i-x-i-p-perezi-i-hybridogenetic-complex-based-on-16-newly-characterised-microsatellite-markers?format=html</guid>
           <description><![CDATA[<p>pp. 99-108</p><p><em>&#65279;Authors:&#160;</em>&#65279;Gregorio S&#225;nchez-Montes, Ernesto Recuero, Jorge Guti&#233;rrez-Rodr&#237;guez,&#160;Ivan Gomez-Mestre &amp; I&#241;igo Mart&#237;nez-Solano</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;<em>Pelophylax perezi</em> is an Iberian green waterfrog with high tolerance to habitat alteration that at times shows local population growth and demographic expansion, even where other species decline. However, pond destruction, invasive predators and hybridisation with other European waterfrog species (<em>P. ridibundus</em>) threaten many of its populations across its range. Hybrids of <em>P. perezi</em> and <em>P. ridibundus</em> (<em>P. kl. grafi</em>) can breed successfully with the former parental species after discarding the whole <em>P. perezi</em> genome in the germinal line, thus representing a sexual parasite for <em>P. perez</em>i. However, little is known about the extent of the contact zone of this hybridogenetic complex. Due to the morphological similarity of the three taxa, molecular tools are needed to delineate their respective ranges. Here we characterise a set of 16 microsatellite markers specifically developed for <em>P. perezi</em>. These markers showed moderate to high polymorphism (2&#8211;17 alleles/locus) in two populations from central Spain (<em>n</em>=20 and <em>n</em>=23), allowing individual identification of frogs. Seven of these markers cross-amplified in individuals of P. ridibundus from southern France (3&#8211;8 alleles/locus). These markers were used to genotype samples along a transect from southern France to eastern Spain, encompassing both pure and hybrid individuals. Sample assignment to each taxon was based on the new microsatellite loci and compared with nuclear and mitochondrial sequence data. Our results show that these markers are useful to distinguish <em>P. ridibundus</em>, <em>P. perezi</em> and the hybrid form <em>P. kl. grafi</em> from each other, even when sample sizes are low. The newly characterised markers will also be useful in demographic and phylogeographic studies in <em>P. perezi</em> and are thus a valuable tool for evolutionary and conservation oriented research.</p>
<p><strong>&#65279;Key words:&#160;</strong>&#65279;cross-amplification, hybridisation, microsatellites, <em>Pelophylax kl. grafi</em>, <em>Pelophylax perezi,</em> <em>Pelophylax ridibundus</em></p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>06. Genetic differentiation and population dynamics of Alpine salamanders ([i]Salamandra atra[/i], Laurenti 1768) in Southeastern Alps and Dinarides</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/867-06-genetic-differentiation-and-population-dynamics-of-alpine-salamanders-i-salamandra-atra-i-laurenti-1768-in-southeastern-alps-and-dinarides?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/867-06-genetic-differentiation-and-population-dynamics-of-alpine-salamanders-i-salamandra-atra-i-laurenti-1768-in-southeastern-alps-and-dinarides/file" length="1869323" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/867-06-genetic-differentiation-and-population-dynamics-of-alpine-salamanders-i-salamandra-atra-i-laurenti-1768-in-southeastern-alps-and-dinarides/file"
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           <media:title type="plain">06. Genetic differentiation and population dynamics of Alpine salamanders ([i]Salamandra atra[/i], Laurenti 1768) in Southeastern Alps and Dinarides</media:title>
           <media:description type="html"><![CDATA[<p>pp. 109-117</p><p><em>&#65279;Authors:&#160;</em>&#65279;Andrej Razpet, Emina &#352;unje, Belma Kalamuji&#263;, Una Tuli&#263;, Naris Pojski&#263;, David Stankovi&#263;,&#160;Imre Krizmani&#263; &amp; Sa&#353;a Mari&#263;</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;The genetic structure of Alpine salamander (<em>Salamandra atra</em>, Laurenti 1768) populations in the Dinarides with respect to continuous populations in the Alps is still poorly understood. To compare Dinaric populations with the nearest Alpine populations, eleven populations were genotyped using seven microsatellite loci. Two major groups were detected: a more diverse Alpine group in the Steiner and Julian Alps, and a less diverse Dinaric group. The Pokljuka population was assigned to the Dinaric group despite its geographical location in the Alps, placing the divide between major groups north of the southern Alpine orographic boundary. Bottlenecks dated at the end of the last glaciation event were suggested for Alpine populations, but not for Dinaric populations. Genetic signatures of migration were detected within Dinaric and Alpine regions, but not between them. Populations from the Prenj Mountain (Bosnia-Herzegovina), where the subspecies <em>S. atra</em> prenjensis was described, were not genetically distinct from other Dinaric populations. These results suggest that, if the taxon remains valid, <em>S. atra</em> <em>prenjensis</em> should include the entire Dinarides as well as the Pokljuka population located in the Alps.</p>
<p><strong>&#65279;Key words:&#160;</strong>&#65279;Alpine salamander, Alps, Dinarides, genetic diversity, microsatellites, population history</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/867-06-genetic-differentiation-and-population-dynamics-of-alpine-salamanders-i-salamandra-atra-i-laurenti-1768-in-southeastern-alps-and-dinarides?format=html</guid>
           <description><![CDATA[<p>pp. 109-117</p><p><em>&#65279;Authors:&#160;</em>&#65279;Andrej Razpet, Emina &#352;unje, Belma Kalamuji&#263;, Una Tuli&#263;, Naris Pojski&#263;, David Stankovi&#263;,&#160;Imre Krizmani&#263; &amp; Sa&#353;a Mari&#263;</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;The genetic structure of Alpine salamander (<em>Salamandra atra</em>, Laurenti 1768) populations in the Dinarides with respect to continuous populations in the Alps is still poorly understood. To compare Dinaric populations with the nearest Alpine populations, eleven populations were genotyped using seven microsatellite loci. Two major groups were detected: a more diverse Alpine group in the Steiner and Julian Alps, and a less diverse Dinaric group. The Pokljuka population was assigned to the Dinaric group despite its geographical location in the Alps, placing the divide between major groups north of the southern Alpine orographic boundary. Bottlenecks dated at the end of the last glaciation event were suggested for Alpine populations, but not for Dinaric populations. Genetic signatures of migration were detected within Dinaric and Alpine regions, but not between them. Populations from the Prenj Mountain (Bosnia-Herzegovina), where the subspecies <em>S. atra</em> prenjensis was described, were not genetically distinct from other Dinaric populations. These results suggest that, if the taxon remains valid, <em>S. atra</em> <em>prenjensis</em> should include the entire Dinarides as well as the Pokljuka population located in the Alps.</p>
<p><strong>&#65279;Key words:&#160;</strong>&#65279;Alpine salamander, Alps, Dinarides, genetic diversity, microsatellites, population history</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>06. Appendix</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/868-06-appendix?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/868-06-appendix/file" length="481424" type="application/pdf" />
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           <media:title type="plain">06. Appendix</media:title>
           <media:description type="html"><![CDATA[<p>Online appendex for 06.&#160;Genetic differentiation and population dynamics of Alpine salamanders (Salamandra atra, Laurenti 1768) in Southeastern Alps and Dinarides</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/868-06-appendix?format=html</guid>
           <description><![CDATA[<p>Online appendex for 06.&#160;Genetic differentiation and population dynamics of Alpine salamanders (Salamandra atra, Laurenti 1768) in Southeastern Alps and Dinarides</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>07. Reproductive biology of the southernmost [i]Kentropyx[/i] lizard from the Wet Chaco of Corrientes, Argentina</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/869-07-reproductive-biology-of-the-southernmost-i-kentropyx-i-lizard-from-the-wet-chaco-of-corrientes-argentina?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/869-07-reproductive-biology-of-the-southernmost-i-kentropyx-i-lizard-from-the-wet-chaco-of-corrientes-argentina/file" length="4698727" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/869-07-reproductive-biology-of-the-southernmost-i-kentropyx-i-lizard-from-the-wet-chaco-of-corrientes-argentina/file"
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           <media:title type="plain">07. Reproductive biology of the southernmost [i]Kentropyx[/i] lizard from the Wet Chaco of Corrientes, Argentina</media:title>
           <media:description type="html"><![CDATA[<p>pp. 119-130</p><p><em>Authors:</em>&#65279;&#160;Mart&#237;n A. Ortiz, Jorgelina M. Boretto &amp; Nora R. Ibarg&#252;engoyt&#237;a</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;Studies on reproductive modes, size at maturity, clutch size and clutch frequency have contributed greatly to our understanding of life history variation among lizard populations, and thereby, to implement conservation strategies. Herein, we studied the reproductive biology of the vulnerable tegu lizard <em>Kentropyx</em> <em>viridistriga</em> from Corrientes, northeastern Argentina (Wet Chaco). <em>Kentropyx</em> <em>viridistriga</em> are active from early summer to late autumn, with temperature and photoperiod influencing the timing of reproduction and the brumation period. Females showed an annual reproductive cycle, and males exhibited a continuous reproductive cycle during the activity season. Females laid at least two clutches of on average three eggs per reproductive season. Neonates occured in spring, and reached sexual maturity in the first year of life. Females reached sexual maturity at a larger snout-vent length (64.1 mm) than males (54.8 mm). Sexual dimorphism is evident, with males showing greater head size and longer tails than females, while females exhibit larger interlimb length than males. This study reveals that the reproductive strategy of <em>K</em>. <em>viridistriga</em> is adjusted to the environmental conditions of the southernmost distribution for the genus.</p>
<p>&#65279;<strong>Key words:&#160;</strong>&#65279;life history,<em> Kentropyx viridistriga</em>, reproductive cycle, Squamata, Teiidae</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/869-07-reproductive-biology-of-the-southernmost-i-kentropyx-i-lizard-from-the-wet-chaco-of-corrientes-argentina?format=html</guid>
           <description><![CDATA[<p>pp. 119-130</p><p><em>Authors:</em>&#65279;&#160;Mart&#237;n A. Ortiz, Jorgelina M. Boretto &amp; Nora R. Ibarg&#252;engoyt&#237;a</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;Studies on reproductive modes, size at maturity, clutch size and clutch frequency have contributed greatly to our understanding of life history variation among lizard populations, and thereby, to implement conservation strategies. Herein, we studied the reproductive biology of the vulnerable tegu lizard <em>Kentropyx</em> <em>viridistriga</em> from Corrientes, northeastern Argentina (Wet Chaco). <em>Kentropyx</em> <em>viridistriga</em> are active from early summer to late autumn, with temperature and photoperiod influencing the timing of reproduction and the brumation period. Females showed an annual reproductive cycle, and males exhibited a continuous reproductive cycle during the activity season. Females laid at least two clutches of on average three eggs per reproductive season. Neonates occured in spring, and reached sexual maturity in the first year of life. Females reached sexual maturity at a larger snout-vent length (64.1 mm) than males (54.8 mm). Sexual dimorphism is evident, with males showing greater head size and longer tails than females, while females exhibit larger interlimb length than males. This study reveals that the reproductive strategy of <em>K</em>. <em>viridistriga</em> is adjusted to the environmental conditions of the southernmost distribution for the genus.</p>
<p>&#65279;<strong>Key words:&#160;</strong>&#65279;life history,<em> Kentropyx viridistriga</em>, reproductive cycle, Squamata, Teiidae</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>08. Habitat use by grass snakes and three sympatric lizard species on lowland heath managed using ‘conservation grazing’</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/870-08-habitat-use-by-grass-snakes-and-three-sympatric-lizard-species-on-lowland-heath-managed-using-conservation-grazing?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/870-08-habitat-use-by-grass-snakes-and-three-sympatric-lizard-species-on-lowland-heath-managed-using-conservation-grazing/file" length="716422" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/870-08-habitat-use-by-grass-snakes-and-three-sympatric-lizard-species-on-lowland-heath-managed-using-conservation-grazing/file"
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           <media:title type="plain">08. Habitat use by grass snakes and three sympatric lizard species on lowland heath managed using ‘conservation grazing’</media:title>
           <media:description type="html"><![CDATA[<p>&#65279;pp. 131-138</p><p><em>&#65279;Authors:&#160;</em>&#65279;Christopher J. Reading &amp; Gabriela M. Jofr&#233;</p>
<p><strong>Abstract:&#160;</strong>&#65279;Cattle grazing is being used increasingly by landowners and statutory conservation bodies to manage heathlands in parts of mainland Europe and in the UK, where it is called &#8216;conservation grazing&#8217;. Between 2010 and 2013, cattle were excluded from six hectares of lowland heath, in southern England, that had been subject to annual summer cattle grazing between May 1997 and autumn 2009. Changes in grass snake <em>Natrix</em> <em>natrix</em>, common lizard <em>Zootoca</em> <em>vivipara</em>, slow worm <em>Anguis</em> <em>fragilis</em> and sand lizard <em>Lacerta</em> <em>agilis</em> numbers were recorded annually in the ungrazed area and in a four hectare area of heathland adjacent to it that continued to be grazed. The number of grass snake, common lizard and slow worm sightings were significantly higher in the ungrazed heath than the grazed heath and were associated with increased habitat structure, resulting principally from increased height and cover of grasses, particularly <em>Molinia</em> <em>caerulea</em>. Conversely, there was no significant difference in the number of adult sand lizard sightings between the grazed and ungrazed heath though sighting frequency was inversely correlated with both grass and grass litter cover. Our results suggest that the use of cattle grazing as a management tool on lowland heath is detrimental to grass snake, slow worm and common lizard populations but may be less so to adult sand lizards. Although newborn slow worms and common lizards were observed throughout the study area, significantly fewer were found in the grazed areas than the ungrazed areas. The absence of newborn grass snakes and sand lizards in the grazed areas suggests that successful breeding had not occurred in these areas.</p>
<p><strong>&#65279;Key words</strong>&#65279;:&#160;<em>Anguis fragilis, Calluna vulgaris</em>, cattle grazing, habitat structure, <em>Lacerta agilis, Molinia caerulea,&#160;</em><em>Natrix natrix, Zootoca vivipara,</em></p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/870-08-habitat-use-by-grass-snakes-and-three-sympatric-lizard-species-on-lowland-heath-managed-using-conservation-grazing?format=html</guid>
           <description><![CDATA[<p>&#65279;pp. 131-138</p><p><em>&#65279;Authors:&#160;</em>&#65279;Christopher J. Reading &amp; Gabriela M. Jofr&#233;</p>
<p><strong>Abstract:&#160;</strong>&#65279;Cattle grazing is being used increasingly by landowners and statutory conservation bodies to manage heathlands in parts of mainland Europe and in the UK, where it is called &#8216;conservation grazing&#8217;. Between 2010 and 2013, cattle were excluded from six hectares of lowland heath, in southern England, that had been subject to annual summer cattle grazing between May 1997 and autumn 2009. Changes in grass snake <em>Natrix</em> <em>natrix</em>, common lizard <em>Zootoca</em> <em>vivipara</em>, slow worm <em>Anguis</em> <em>fragilis</em> and sand lizard <em>Lacerta</em> <em>agilis</em> numbers were recorded annually in the ungrazed area and in a four hectare area of heathland adjacent to it that continued to be grazed. The number of grass snake, common lizard and slow worm sightings were significantly higher in the ungrazed heath than the grazed heath and were associated with increased habitat structure, resulting principally from increased height and cover of grasses, particularly <em>Molinia</em> <em>caerulea</em>. Conversely, there was no significant difference in the number of adult sand lizard sightings between the grazed and ungrazed heath though sighting frequency was inversely correlated with both grass and grass litter cover. Our results suggest that the use of cattle grazing as a management tool on lowland heath is detrimental to grass snake, slow worm and common lizard populations but may be less so to adult sand lizards. Although newborn slow worms and common lizards were observed throughout the study area, significantly fewer were found in the grazed areas than the ungrazed areas. The absence of newborn grass snakes and sand lizards in the grazed areas suggests that successful breeding had not occurred in these areas.</p>
<p><strong>&#65279;Key words</strong>&#65279;:&#160;<em>Anguis fragilis, Calluna vulgaris</em>, cattle grazing, habitat structure, <em>Lacerta agilis, Molinia caerulea,&#160;</em><em>Natrix natrix, Zootoca vivipara,</em></p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>08. Appendix</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/871-08-appendix?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/871-08-appendix/file" length="563018" type="application/pdf" />
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           <media:title type="plain">08. Appendix</media:title>
           <media:description type="html"><![CDATA[<p>Online appendix for&#160;&#65279;08. Habitat use by grass snakes and three sympatric lizard species on lowland heath managed using &#8216;conservation grazing&#8217;.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/871-08-appendix?format=html</guid>
           <description><![CDATA[<p>Online appendix for&#160;&#65279;08. Habitat use by grass snakes and three sympatric lizard species on lowland heath managed using &#8216;conservation grazing&#8217;.</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>09. Calls and tadpoles of the species of [i]Pseudis[/i] (Anura, Hylidae, Pseudae)</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/872-09-calls-and-tadpoles-of-the-species-of-i-pseudis-i-anura-hylidae-pseudae?format=html</link>
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           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/872-09-calls-and-tadpoles-of-the-species-of-i-pseudis-i-anura-hylidae-pseudae/file"
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           <media:title type="plain">09. Calls and tadpoles of the species of [i]Pseudis[/i] (Anura, Hylidae, Pseudae)</media:title>
           <media:description type="html"><![CDATA[<p>pp. 139-148</p><p><em>Authors:&#160;</em>&#65279;Diego Jos&#233; Santana, Felipe de Medeiros Magalh&#227;es, Vin&#237;cius de Avelar S&#227;o Pedro, Sarah&#160;M&#226;ngia, Talita Ferreira Amado &amp; Adrian Antonio Garda</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;The use of larval and bioacoustical characters has been essential to solve taxonomic problems of many anuran species. Herein, we describe the advertisement call and tadpoles of <em>Pseudis</em> <em>fusca</em> and<em> P. tocantins</em> and compare them with descriptions of all other Pseudae. The advertisement calls of <em>Pseudis</em> species are formed by pulsed notes. In <em>P. cardosoi</em> and <em>P. minuta</em> all pulses within a single note are concatenated, while in <em>P. bolbodactyla, P. fusca, P. paradoxa</em> and <em>P. tocantins</em> the notes are formed by sets of concatenated pulses. Moreover, the calls of <em>P. bolbodactyla, P. fusca</em> and<em> P. paradoxa</em> are indistinguishable. Tadpoles of<em> P. fusca</em> and<em> P. tocantins</em> resemble other <em>Pseudis</em> tadpoles described so far: their body is oval-shaped in dorsal view and triangular in lateral view and higher than wide; they possess an anteroventral oral disc with five tooth rows (two anterior and three posterior) and well developed tail musculature. The large larval size is in agreement with other species in the genus. We evaluate which characters best distinguish species within <em>Pseudis</em>.</p>
<p><strong>Key words:&#160;</strong>&#65279;bioacoustics, hydrographic basins, larvae, paradoxical frogs, taxonomy</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/872-09-calls-and-tadpoles-of-the-species-of-i-pseudis-i-anura-hylidae-pseudae?format=html</guid>
           <description><![CDATA[<p>pp. 139-148</p><p><em>Authors:&#160;</em>&#65279;Diego Jos&#233; Santana, Felipe de Medeiros Magalh&#227;es, Vin&#237;cius de Avelar S&#227;o Pedro, Sarah&#160;M&#226;ngia, Talita Ferreira Amado &amp; Adrian Antonio Garda</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;The use of larval and bioacoustical characters has been essential to solve taxonomic problems of many anuran species. Herein, we describe the advertisement call and tadpoles of <em>Pseudis</em> <em>fusca</em> and<em> P. tocantins</em> and compare them with descriptions of all other Pseudae. The advertisement calls of <em>Pseudis</em> species are formed by pulsed notes. In <em>P. cardosoi</em> and <em>P. minuta</em> all pulses within a single note are concatenated, while in <em>P. bolbodactyla, P. fusca, P. paradoxa</em> and <em>P. tocantins</em> the notes are formed by sets of concatenated pulses. Moreover, the calls of <em>P. bolbodactyla, P. fusca</em> and<em> P. paradoxa</em> are indistinguishable. Tadpoles of<em> P. fusca</em> and<em> P. tocantins</em> resemble other <em>Pseudis</em> tadpoles described so far: their body is oval-shaped in dorsal view and triangular in lateral view and higher than wide; they possess an anteroventral oral disc with five tooth rows (two anterior and three posterior) and well developed tail musculature. The large larval size is in agreement with other species in the genus. We evaluate which characters best distinguish species within <em>Pseudis</em>.</p>
<p><strong>Key words:&#160;</strong>&#65279;bioacoustics, hydrographic basins, larvae, paradoxical frogs, taxonomy</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>10. Chemical discrimination of sympatric snakes by the mountain lizard [i]Iberolacerta galani[/i] (Squamata: Lacertidae)</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/873-10-chemical-discrimination-of-sympatric-snakes-by-the-mountain-lizard-i-iberolacerta-galani-i-squamata-lacertidae?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/873-10-chemical-discrimination-of-sympatric-snakes-by-the-mountain-lizard-i-iberolacerta-galani-i-squamata-lacertidae/file" length="827253" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/873-10-chemical-discrimination-of-sympatric-snakes-by-the-mountain-lizard-i-iberolacerta-galani-i-squamata-lacertidae/file"
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           <media:title type="plain">10. Chemical discrimination of sympatric snakes by the mountain lizard [i]Iberolacerta galani[/i] (Squamata: Lacertidae)</media:title>
           <media:description type="html"><![CDATA[<p>pp. 149-155</p><p><em>&#65279;Authors:&#160;</em>&#65279;Abraham Menc&#237;a, Zaida Ortega &amp; Valent&#237;n P&#233;rez-Mellado</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;We conducted an experiment on chemical discrimination of two saurophagous snakes (the smooth snake, <em>Coronella</em> <em>austriaca</em> and the Seoane's viper, <em>Vipera</em> <em>seoanei</em>) as well as the aquatic <em>Natrix</em> <em>maura</em>, by the mountain lizard <em>Iberolacerta</em> <em>galani</em>. Using terraria, 24 lizards were exposed to scents by the three snakes as well as an odourless control. We quantified fourteen behavioural variables, twelve of which significantly differed among treatments. Lizards are able to recognise the scents of both predatory snakes, and react to them with intense antipredatory responses. The antipredatory behaviour found in <em>I. galani</em> was similar for the scents of the two different predatory snakes, despite differences in their foraging behaviour. The behaviour displayed by lizards confronted with chemical cues suggests an adaptation to minimise the likelihood of being attacked.</p>
<p><strong>Key words:&#160;</strong>&#65279;antipredatory behaviour, chemoreception, <em>Iberolacerta</em> <em>galani</em>, Lacertidae, Reptiles, Squamata</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/873-10-chemical-discrimination-of-sympatric-snakes-by-the-mountain-lizard-i-iberolacerta-galani-i-squamata-lacertidae?format=html</guid>
           <description><![CDATA[<p>pp. 149-155</p><p><em>&#65279;Authors:&#160;</em>&#65279;Abraham Menc&#237;a, Zaida Ortega &amp; Valent&#237;n P&#233;rez-Mellado</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;We conducted an experiment on chemical discrimination of two saurophagous snakes (the smooth snake, <em>Coronella</em> <em>austriaca</em> and the Seoane's viper, <em>Vipera</em> <em>seoanei</em>) as well as the aquatic <em>Natrix</em> <em>maura</em>, by the mountain lizard <em>Iberolacerta</em> <em>galani</em>. Using terraria, 24 lizards were exposed to scents by the three snakes as well as an odourless control. We quantified fourteen behavioural variables, twelve of which significantly differed among treatments. Lizards are able to recognise the scents of both predatory snakes, and react to them with intense antipredatory responses. The antipredatory behaviour found in <em>I. galani</em> was similar for the scents of the two different predatory snakes, despite differences in their foraging behaviour. The behaviour displayed by lizards confronted with chemical cues suggests an adaptation to minimise the likelihood of being attacked.</p>
<p><strong>Key words:&#160;</strong>&#65279;antipredatory behaviour, chemoreception, <em>Iberolacerta</em> <em>galani</em>, Lacertidae, Reptiles, Squamata</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>11. How to form a group: effects of heterospecifics, kinship and familiarity in the grouping preference of green and golden bell frog tadpoles</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/874-11-how-to-form-a-group-effects-of-heterospecifics-kinship-and-familiarity-in-the-grouping-preference-of-green-and-golden-bell-frog-tadpoles?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/874-11-how-to-form-a-group-effects-of-heterospecifics-kinship-and-familiarity-in-the-grouping-preference-of-green-and-golden-bell-frog-tadpoles/file" length="706917" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/874-11-how-to-form-a-group-effects-of-heterospecifics-kinship-and-familiarity-in-the-grouping-preference-of-green-and-golden-bell-frog-tadpoles/file"
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           <media:title type="plain">11. How to form a group: effects of heterospecifics, kinship and familiarity in the grouping preference of green and golden bell frog tadpoles</media:title>
           <media:description type="html"><![CDATA[<p>pp. 157-164</p><p><em>&#65279;Authors:&#160;</em>&#65279;L&#237;gia Pizzatto, Michelle Stockwell, Simon Clulow, John Clulow &amp; Michael Mahony</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;Social aggregations are widespread among animal groups. They are relatively common in amphibian larvae, likely conferring protection against predators, advantages for microhabitat selection, foraging efficiency, and thermoregulatory efficiency. Group formation involves selection of individuals to group with by the other members, and several tadpoles are reported to recognise and prefer to aggregate with siblings or familiar individuals. In Australia, tadpoles of the endangered green and golden bell frog, <em>Litoria</em> <em>aurea</em>, are attracted to conspecifics and form schools. We conducted two choice experiments for captive breed tadpoles of this species to test their grouping preferences. Tadpoles preferred to aggregate with conspecifics to heterospecifics of a sympatric species; however, when conspecifics were absent they preferred to aggregate with the heterospecifcs than to remain alone. Tadpoles also preferred unfamiliar kin to unfamiliar non-kin conspecifics, but had no preferences between unfamiliar and familiar siblings. Once widespread in southeast Australia, the green and golden bell frog has suffered considerable declines and local extinctions in recent decades. Susceptibility to chytridiomycosis is likely the major threat for most remaining fragmented populations and the major challenge for reintroduction programs. The strong gregarious behaviour of this species may affect disease dynamics, especially chytridiomicosis that continues to threaten remaining wild populations.</p>
<p><strong>Key words:&#160;</strong>&#65279;amphibian, conspecific attraction, familiarity, grouping, kin recognition, <em>Litoria aurea</em></p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/874-11-how-to-form-a-group-effects-of-heterospecifics-kinship-and-familiarity-in-the-grouping-preference-of-green-and-golden-bell-frog-tadpoles?format=html</guid>
           <description><![CDATA[<p>pp. 157-164</p><p><em>&#65279;Authors:&#160;</em>&#65279;L&#237;gia Pizzatto, Michelle Stockwell, Simon Clulow, John Clulow &amp; Michael Mahony</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;Social aggregations are widespread among animal groups. They are relatively common in amphibian larvae, likely conferring protection against predators, advantages for microhabitat selection, foraging efficiency, and thermoregulatory efficiency. Group formation involves selection of individuals to group with by the other members, and several tadpoles are reported to recognise and prefer to aggregate with siblings or familiar individuals. In Australia, tadpoles of the endangered green and golden bell frog, <em>Litoria</em> <em>aurea</em>, are attracted to conspecifics and form schools. We conducted two choice experiments for captive breed tadpoles of this species to test their grouping preferences. Tadpoles preferred to aggregate with conspecifics to heterospecifics of a sympatric species; however, when conspecifics were absent they preferred to aggregate with the heterospecifcs than to remain alone. Tadpoles also preferred unfamiliar kin to unfamiliar non-kin conspecifics, but had no preferences between unfamiliar and familiar siblings. Once widespread in southeast Australia, the green and golden bell frog has suffered considerable declines and local extinctions in recent decades. Susceptibility to chytridiomycosis is likely the major threat for most remaining fragmented populations and the major challenge for reintroduction programs. The strong gregarious behaviour of this species may affect disease dynamics, especially chytridiomicosis that continues to threaten remaining wild populations.</p>
<p><strong>Key words:&#160;</strong>&#65279;amphibian, conspecific attraction, familiarity, grouping, kin recognition, <em>Litoria aurea</em></p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>12. Morphological variation within [i]Thamnodynastes pallidus[/i] (Linnaeus, 1758) (Serpentes: Dipsadidae: Xenodontinae: Tachymenini)</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/875-12-morphological-variation-within-i-thamnodynastes-pallidus-i-linnaeus-1758-serpentes-dipsadidae-xenodontinae-tachymenini?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/875-12-morphological-variation-within-i-thamnodynastes-pallidus-i-linnaeus-1758-serpentes-dipsadidae-xenodontinae-tachymenini/file" length="3465117" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/875-12-morphological-variation-within-i-thamnodynastes-pallidus-i-linnaeus-1758-serpentes-dipsadidae-xenodontinae-tachymenini/file"
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           <media:title type="plain">12. Morphological variation within [i]Thamnodynastes pallidus[/i] (Linnaeus, 1758) (Serpentes: Dipsadidae: Xenodontinae: Tachymenini)</media:title>
           <media:description type="html"><![CDATA[<p>pp. 165-174</p>
<p><em>Authors:&nbsp;</em>Romulo Pantoja Nóbrega, Giovanna Gondim Montingelli, Vivian Trevine, Francisco Luis&nbsp;Franco, Gustavo H.C. Vieira, Gabriel C. Costa &amp; Daniel Oliveira Mesquita</p>
<p><strong>Abstract:&nbsp;</strong>The genus <em>Thamnodynastes</em> is comprised of 19 valid species distributed throughout South America. <em>Thamnodynastes</em> <em>pallidus</em> is associated with the Amazon region and the Atlantic forest of northeastern Brazil, exhibiting a disjunct distribution. The characters employed in the definition of this species are controversial, and its morphological variation is poorly known. Some authors do not consider its distribution in the Atlantic Forest, attributing these specimens to <em>T. almae</em>. This study aims to compare the Amazonian and the Atlantic populations of <em>T. pallidus</em> by performing an analysis of morphological (colouration, morphometry, pholidosis and hemipenial morphology) and geographical variations. We examined 70 specimens of T. pallidus from the Atlantic Forest, and 61 from the Amazon Forest. A logistic regression selected the number of infralabials, number of subcaudals, and snout length as the only predictors that could discriminate the two populations. The distribution model shows regions with higher climatic suitability for <em>T. pallidus</em> spread across the Amazon basin and the Atlantic Forest. We provide sufficient evidence to characterise <em>T. pallidus</em>, and differentiate it from its congeners. Although we demonstrate the occurrence of variation with respect to some meristic and hemipenial characters between and within each population, we conclude that these variations are not sufficient to recognise them as distinct species.&nbsp;&nbsp;</p>
<p><strong>Key words:&nbsp;</strong>Amazon Forest, Atlantic Forest, hemipenis, pholidosis, South America, Squamata</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/875-12-morphological-variation-within-i-thamnodynastes-pallidus-i-linnaeus-1758-serpentes-dipsadidae-xenodontinae-tachymenini?format=html</guid>
           <description><![CDATA[<p>pp. 165-174</p>
<p><em>Authors:&nbsp;</em>Romulo Pantoja Nóbrega, Giovanna Gondim Montingelli, Vivian Trevine, Francisco Luis&nbsp;Franco, Gustavo H.C. Vieira, Gabriel C. Costa &amp; Daniel Oliveira Mesquita</p>
<p><strong>Abstract:&nbsp;</strong>The genus <em>Thamnodynastes</em> is comprised of 19 valid species distributed throughout South America. <em>Thamnodynastes</em> <em>pallidus</em> is associated with the Amazon region and the Atlantic forest of northeastern Brazil, exhibiting a disjunct distribution. The characters employed in the definition of this species are controversial, and its morphological variation is poorly known. Some authors do not consider its distribution in the Atlantic Forest, attributing these specimens to <em>T. almae</em>. This study aims to compare the Amazonian and the Atlantic populations of <em>T. pallidus</em> by performing an analysis of morphological (colouration, morphometry, pholidosis and hemipenial morphology) and geographical variations. We examined 70 specimens of T. pallidus from the Atlantic Forest, and 61 from the Amazon Forest. A logistic regression selected the number of infralabials, number of subcaudals, and snout length as the only predictors that could discriminate the two populations. The distribution model shows regions with higher climatic suitability for <em>T. pallidus</em> spread across the Amazon basin and the Atlantic Forest. We provide sufficient evidence to characterise <em>T. pallidus</em>, and differentiate it from its congeners. Although we demonstrate the occurrence of variation with respect to some meristic and hemipenial characters between and within each population, we conclude that these variations are not sufficient to recognise them as distinct species.&nbsp;&nbsp;</p>
<p><strong>Key words:&nbsp;</strong>Amazon Forest, Atlantic Forest, hemipenis, pholidosis, South America, Squamata</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>13. Mitochondrial phylogeny of the [i]Darevskia saxicola[/i] complex: two highly deviant evolutionary lineages from the easternmost part of the range</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/876-13-mitochondrial-phylogeny-of-the-i-darevskia-saxicola-i-complex-two-highly-deviant-evolutionary-lineages-from-the-easternmost-part-of-the-range?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/876-13-mitochondrial-phylogeny-of-the-i-darevskia-saxicola-i-complex-two-highly-deviant-evolutionary-lineages-from-the-easternmost-part-of-the-range/file" length="1867348" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/876-13-mitochondrial-phylogeny-of-the-i-darevskia-saxicola-i-complex-two-highly-deviant-evolutionary-lineages-from-the-easternmost-part-of-the-range/file"
                fileSize="1867348"
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           <media:title type="plain">13. Mitochondrial phylogeny of the [i]Darevskia saxicola[/i] complex: two highly deviant evolutionary lineages from the easternmost part of the range</media:title>
           <media:description type="html"><![CDATA[<p>pp. 175-182</p>
<p><em>Authors:&nbsp;</em>David Tarkhnishvili, Mariam Gabelaia, Levan Mumladze &amp; Marine Murtskhvaladze</p>
<p><strong>Abstract:&nbsp;</strong>The rock lizards of the <em>Darevskia</em> <em>saxicola</em> complex are found exclusively in the west of the Greater Caucasus and in southern Crimea. The earliest split within this group occurred between <em>D. saxicola</em> from the northern and <em>D. brauneri</em> from the southern slopes of the Greater Caucasus, followed by the split between <em>D. brauneri</em> and the Crimean <em>D. lindholmi</em>, and the expansion of <em>D. saxicola</em> to the westernmost slopes of the Greater Caucasus. We collected nominal<em> D. brauneri</em> from the two easternmost populations of the species range: the valleys of the Tekhuri and Enguri rivers in Georgia. Analysis of mitochondrial DNA showed that the lizards from both valleys are deeply differentiated from each other and from previously characterised <em>D. brauneri</em>. Lizards from Tekhuri keep a basal position within the clade <em>D. saxicola</em> (excluding <em>D. praticola</em>), and lizards from Enguri are closer matrilineally to the northern Caucasian <em>D. saxicola</em> than to either of the populations of nominal <em>D. brauneri</em>. Tekhuri lizards have broader heads and more small scales between the inner and outer rows of supraoculars than the other populations of the group. We suggest that the taxonomy of the group requires revision, considering the multiple deeply divergent mitochondrial lineages and introgressive gene flow between the continental populations of nominal <em>D. saxicola</em> and <em>D. brauneri</em>. The <em>D. saxicola</em> complex in the Caucasus resembles a “ring species” arrangement as described for other taxa and mountain regions.</p>
<p><strong>Key words:&nbsp;</strong>Caucasus, cytochrome b, <em>Darevskia</em>, glacial refugia, mitochondrial DNA, scalation, Species Nova</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/876-13-mitochondrial-phylogeny-of-the-i-darevskia-saxicola-i-complex-two-highly-deviant-evolutionary-lineages-from-the-easternmost-part-of-the-range?format=html</guid>
           <description><![CDATA[<p>pp. 175-182</p>
<p><em>Authors:&nbsp;</em>David Tarkhnishvili, Mariam Gabelaia, Levan Mumladze &amp; Marine Murtskhvaladze</p>
<p><strong>Abstract:&nbsp;</strong>The rock lizards of the <em>Darevskia</em> <em>saxicola</em> complex are found exclusively in the west of the Greater Caucasus and in southern Crimea. The earliest split within this group occurred between <em>D. saxicola</em> from the northern and <em>D. brauneri</em> from the southern slopes of the Greater Caucasus, followed by the split between <em>D. brauneri</em> and the Crimean <em>D. lindholmi</em>, and the expansion of <em>D. saxicola</em> to the westernmost slopes of the Greater Caucasus. We collected nominal<em> D. brauneri</em> from the two easternmost populations of the species range: the valleys of the Tekhuri and Enguri rivers in Georgia. Analysis of mitochondrial DNA showed that the lizards from both valleys are deeply differentiated from each other and from previously characterised <em>D. brauneri</em>. Lizards from Tekhuri keep a basal position within the clade <em>D. saxicola</em> (excluding <em>D. praticola</em>), and lizards from Enguri are closer matrilineally to the northern Caucasian <em>D. saxicola</em> than to either of the populations of nominal <em>D. brauneri</em>. Tekhuri lizards have broader heads and more small scales between the inner and outer rows of supraoculars than the other populations of the group. We suggest that the taxonomy of the group requires revision, considering the multiple deeply divergent mitochondrial lineages and introgressive gene flow between the continental populations of nominal <em>D. saxicola</em> and <em>D. brauneri</em>. The <em>D. saxicola</em> complex in the Caucasus resembles a “ring species” arrangement as described for other taxa and mountain regions.</p>
<p><strong>Key words:&nbsp;</strong>Caucasus, cytochrome b, <em>Darevskia</em>, glacial refugia, mitochondrial DNA, scalation, Species Nova</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>14. Nest predation of the yellow-spotted Amazon River turtle ([i]Podocnemis unifilis[/i], Troschel, 1848) by the fire ant ([i]Solenopsis geminata[/i], Fabricius, 1804) in the Brazilian Amazon</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/877-14-nest-predation-of-the-yellow-spotted-amazon-river-turtle-i-podocnemis-unifilis-i-troschel-1848-by-the-fire-ant-i-solenopsis-geminata-i-fabricius-1804-in-the-brazilian-amazon?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/877-14-nest-predation-of-the-yellow-spotted-amazon-river-turtle-i-podocnemis-unifilis-i-troschel-1848-by-the-fire-ant-i-solenopsis-geminata-i-fabricius-1804-in-the-brazilian-amazon/file" length="1946956" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/877-14-nest-predation-of-the-yellow-spotted-amazon-river-turtle-i-podocnemis-unifilis-i-troschel-1848-by-the-fire-ant-i-solenopsis-geminata-i-fabricius-1804-in-the-brazilian-amazon/file"
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           <media:title type="plain">14. Nest predation of the yellow-spotted Amazon River turtle ([i]Podocnemis unifilis[/i], Troschel, 1848) by the fire ant ([i]Solenopsis geminata[/i], Fabricius, 1804) in the Brazilian Amazon</media:title>
           <media:description type="html"><![CDATA[<p>pp. 183-186</p><p><em>&#65279;Authors:&#160;</em>&#65279;Jos&#233; Erickson &amp; Fabr&#237;cio Baccaro</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;We report the effect of predation by the fire ant <em>Solenopsis</em> <em>geminata</em> on nests of the turtle <em>Podocnemis</em> <em>unifilis</em> in the Piaga&#231;u Purus Sustainable Development Reserve, Amazonas, Brazil. During three consecutive breeding seasons (between September and October of 2012, 2013 and 2014), 492 nests were monitored and 95 (19.3%) were predated. <em>Solenopsis</em> <em>geminata</em> was the main predator, accounting for 65.26% (<em>n</em>=62) of the losses. Nest predation by ants was not correlated with soil exposition time. However, all <em>P. unifilis</em> nests predated by <em>S. geminata</em> were entirely covered by vegetation, suggesting that ants may select nests at specific microhabitat conditions. Studies on larger scales, including areas where <em>S. geminata</em> is naturally absent, are needed to develop an adequate management of<em> P. unifilis</em>.</p>
<p><strong>&#65279;Key words:&#160;</strong>&#65279;fire ant, flooded forest, freshwater turtle,&#160;offspring</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-2-april-2016/877-14-nest-predation-of-the-yellow-spotted-amazon-river-turtle-i-podocnemis-unifilis-i-troschel-1848-by-the-fire-ant-i-solenopsis-geminata-i-fabricius-1804-in-the-brazilian-amazon?format=html</guid>
           <description><![CDATA[<p>pp. 183-186</p><p><em>&#65279;Authors:&#160;</em>&#65279;Jos&#233; Erickson &amp; Fabr&#237;cio Baccaro</p>
<p><strong>&#65279;Abstract:&#160;</strong>&#65279;We report the effect of predation by the fire ant <em>Solenopsis</em> <em>geminata</em> on nests of the turtle <em>Podocnemis</em> <em>unifilis</em> in the Piaga&#231;u Purus Sustainable Development Reserve, Amazonas, Brazil. During three consecutive breeding seasons (between September and October of 2012, 2013 and 2014), 492 nests were monitored and 95 (19.3%) were predated. <em>Solenopsis</em> <em>geminata</em> was the main predator, accounting for 65.26% (<em>n</em>=62) of the losses. Nest predation by ants was not correlated with soil exposition time. However, all <em>P. unifilis</em> nests predated by <em>S. geminata</em> were entirely covered by vegetation, suggesting that ants may select nests at specific microhabitat conditions. Studies on larger scales, including areas where <em>S. geminata</em> is naturally absent, are needed to develop an adequate management of<em> P. unifilis</em>.</p>
<p><strong>&#65279;Key words:&#160;</strong>&#65279;fire ant, flooded forest, freshwater turtle,&#160;offspring</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 2, April 2016</category>
           <pubDate>Mon, 25 Apr 2016 00:00:00 +0100</pubDate>
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