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       <title>Volume 26, Number 3, July 2016 - British Herpetological Society</title>
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       <url>https://www.thebhs.org/joomlatools-files/docman-images/HJ_cover_26_3.png</url>
           <title>Volume 26, Number 3, July 2016 - British Herpetological Society</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016?format=html</link>
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           <title>01. Comparison of female and male vocalisation and larynx morphology in the size dimorphic foot-flagging frog species [i]Staurois guttatus[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/893-01-comparison-of-female-and-male-vocalisation-and-larynx-morphology-in-the-size-dimorphic-foot-flagging-frog-species-i-staurois-guttatus-i?format=html</link>
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           <media:title type="plain">01. Comparison of female and male vocalisation and larynx morphology in the size dimorphic foot-flagging frog species [i]Staurois guttatus[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp. 187-197</p>
<p><em>Authors:&nbsp;</em>Doris Preininger, Stephan Handschuh, Markus Boeckle, Marc Sztatecsny &amp; Walter Hödl</p>
<p><span style="font-size: 12.16px;"><strong>Abstract:</strong>&nbsp;</span><span style="font-size: 12.16px;">In anurans, males have larger laryngeal structures than females and produce conspicuous species-specific calls in various social contexts. Knowledge of female vocalisations is not well established and we start by summarising available spectral and behavioural information on calls in females. We then present novel data on female and male calls in </span><em style="font-size: 12.16px;">Staurois guttatus</em><span style="font-size: 12.16px;"> and ask how larynx morphology influences call characteristics. While there was no difference in the dominant frequency between the sexes, sound pressure of female calls was lower than in males suggesting that they could be masked by ambient stream noise in the natural habitat. In an experimental setup, unreceptive females started calling when approached by a male less than 30 cm away, indicating an agonistic function of calling behaviour. In accordance with the overall size dimorphism in </span><em style="font-size: 12.16px;">S. guttatus</em><span style="font-size: 12.16px;">, laryngeal muscles as analysed by microCT were larger in females than in males whereas a reverse dimorphism was reported for most anuran species with silent and vocal females. We argue that in noisy environments such as streams, small male larynx size associated with high frequency calls is advantageous due to reduced masking and discuss the functional differences and communalities in signalling behaviour between the sexes and in the genus </span><em style="font-size: 12.16px;">Staurois</em><span style="font-size: 12.16px;">.</span></p>
<p><strong>Key words:&nbsp;</strong>&nbsp;anuran, female calls, laryngeal structures, noisy environment, visual signal</p>
<p><span style="font-size: 12.16px;"></span></p>
<p class="MsoNormal">&nbsp;</p>]]></media:description>
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           <description><![CDATA[<p>pp. 187-197</p>
<p><em>Authors:&nbsp;</em>Doris Preininger, Stephan Handschuh, Markus Boeckle, Marc Sztatecsny &amp; Walter Hödl</p>
<p><span style="font-size: 12.16px;"><strong>Abstract:</strong>&nbsp;</span><span style="font-size: 12.16px;">In anurans, males have larger laryngeal structures than females and produce conspicuous species-specific calls in various social contexts. Knowledge of female vocalisations is not well established and we start by summarising available spectral and behavioural information on calls in females. We then present novel data on female and male calls in </span><em style="font-size: 12.16px;">Staurois guttatus</em><span style="font-size: 12.16px;"> and ask how larynx morphology influences call characteristics. While there was no difference in the dominant frequency between the sexes, sound pressure of female calls was lower than in males suggesting that they could be masked by ambient stream noise in the natural habitat. In an experimental setup, unreceptive females started calling when approached by a male less than 30 cm away, indicating an agonistic function of calling behaviour. In accordance with the overall size dimorphism in </span><em style="font-size: 12.16px;">S. guttatus</em><span style="font-size: 12.16px;">, laryngeal muscles as analysed by microCT were larger in females than in males whereas a reverse dimorphism was reported for most anuran species with silent and vocal females. We argue that in noisy environments such as streams, small male larynx size associated with high frequency calls is advantageous due to reduced masking and discuss the functional differences and communalities in signalling behaviour between the sexes and in the genus </span><em style="font-size: 12.16px;">Staurois</em><span style="font-size: 12.16px;">.</span></p>
<p><strong>Key words:&nbsp;</strong>&nbsp;anuran, female calls, laryngeal structures, noisy environment, visual signal</p>
<p><span style="font-size: 12.16px;"></span></p>
<p class="MsoNormal">&nbsp;</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>02. Body size affects digestive performance in a Mediterranean lizard</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/894-02-body-size-affects-digestive-performance-in-a-mediterranean-lizard?format=html</link>
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                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/894-02-body-size-affects-digestive-performance-in-a-mediterranean-lizard/file"
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           <media:title type="plain">02. Body size affects digestive performance in a Mediterranean lizard</media:title>
           <media:description type="html"><![CDATA[<p>pp. 199-205</p><p><em>Authors:&nbsp;</em>P. Pafilis, S. Meiri, K. Sagonas, D. Karakasi, E. Kourelou &amp; E.D. Valakos</p>
<p><strong>Abstract:&nbsp;</strong><span style="font-size: 12.16px;">Effective digestion is decisive for survival. In nature, where most animals feed sporadically, high digestive performance guarantees they will gain the most out of their infrequent meals. Larger body size implies higher energy requirements and digestion should function properly to provide this extra energy. Comparing Skyros wall lizards (</span><em style="font-size: 12.16px;">Podarcis gaigeae</em><span style="font-size: 12.16px;">) from Skyros Island to large (“giant”) lizards from a nearby islet, we tested the hypothesis that digestion in large individuals is more efficient than in small individuals. We anticipated that giant lizards would have higher gut passage time (GPT), longer gastrointestinal (GI) tracts and higher apparent digestive efficiencies (ADE) for lipids, sugars and proteins. These predictions were only partially verified. Giant lizards indeed had longer (than expected based on body length) GI tract and longer GPTs but achieved higher ADE only for proteins, while ADEs for lipids and sugars did not differ from the normal-sized lizards. We postulated that the observed deviations from the typical digestive pattern are explained by cannibalism being more prominent on the islet. Giant lizards regularly consume tail fragments of their conspecifics and even entire juveniles. To break down their hard-to-digest vertebrate prey, they need to extend GPT and thus they have developed a longer GI tract. Also, to fuel tail regeneration they have to raise ADEproteins. It seems that larger size, through the evolution of longer GI tract, enables giant lizards to take advantage of tails lost in agonistic encounters as a valuable food source.</span><span style="font-size: 12.16px;"></span></p>
<p class="MsoNormal">&nbsp;<strong>Key words:&nbsp;</strong>&nbsp;body size, cannibalism, digestion, gigantism, islands, reptiles</p>
<p><span style="font-size: 12.16px;"></span></p>
<p><span style="font-size: 12.16px;"></span></p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/894-02-body-size-affects-digestive-performance-in-a-mediterranean-lizard?format=html</guid>
           <description><![CDATA[<p>pp. 199-205</p><p><em>Authors:&nbsp;</em>P. Pafilis, S. Meiri, K. Sagonas, D. Karakasi, E. Kourelou &amp; E.D. Valakos</p>
<p><strong>Abstract:&nbsp;</strong><span style="font-size: 12.16px;">Effective digestion is decisive for survival. In nature, where most animals feed sporadically, high digestive performance guarantees they will gain the most out of their infrequent meals. Larger body size implies higher energy requirements and digestion should function properly to provide this extra energy. Comparing Skyros wall lizards (</span><em style="font-size: 12.16px;">Podarcis gaigeae</em><span style="font-size: 12.16px;">) from Skyros Island to large (“giant”) lizards from a nearby islet, we tested the hypothesis that digestion in large individuals is more efficient than in small individuals. We anticipated that giant lizards would have higher gut passage time (GPT), longer gastrointestinal (GI) tracts and higher apparent digestive efficiencies (ADE) for lipids, sugars and proteins. These predictions were only partially verified. Giant lizards indeed had longer (than expected based on body length) GI tract and longer GPTs but achieved higher ADE only for proteins, while ADEs for lipids and sugars did not differ from the normal-sized lizards. We postulated that the observed deviations from the typical digestive pattern are explained by cannibalism being more prominent on the islet. Giant lizards regularly consume tail fragments of their conspecifics and even entire juveniles. To break down their hard-to-digest vertebrate prey, they need to extend GPT and thus they have developed a longer GI tract. Also, to fuel tail regeneration they have to raise ADEproteins. It seems that larger size, through the evolution of longer GI tract, enables giant lizards to take advantage of tails lost in agonistic encounters as a valuable food source.</span><span style="font-size: 12.16px;"></span></p>
<p class="MsoNormal">&nbsp;<strong>Key words:&nbsp;</strong>&nbsp;body size, cannibalism, digestion, gigantism, islands, reptiles</p>
<p><span style="font-size: 12.16px;"></span></p>
<p><span style="font-size: 12.16px;"></span></p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>03. Salinity and thermal tolerance of Japanese stream tree frog ([i]Buergeria japonica[/i]) tadpoles from island populations</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/895-03-salinity-and-thermal-tolerance-of-japanese-stream-tree-frog-i-buergeria-japonica-i-tadpoles-from-island-populations?format=html</link>
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           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/895-03-salinity-and-thermal-tolerance-of-japanese-stream-tree-frog-i-buergeria-japonica-i-tadpoles-from-island-populations/file"
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           <media:title type="plain">03. Salinity and thermal tolerance of Japanese stream tree frog ([i]Buergeria japonica[/i]) tadpoles from island populations</media:title>
           <media:description type="html"><![CDATA[<p>pp. 207-211</p><p><em>Authors:&nbsp;</em>Shohei Komaki, Takeshi Igawa, Si-Min Lin &amp; Masayuki Sumida</p>
<p><span style="font-size: 12.16px;"><strong>Abstract:&nbsp;</strong></span><span style="font-size: 12.16px;">Physiological tolerance to variable environmental conditions is essential for species to disperse over habitat boundaries and sustain populations in new habitats. In particular, salinity and temperature are one of the major factors determining species’ distributions. The tree frog </span><em style="font-size: 12.16px;">Buergeria japonica</em><span style="font-size: 12.16px;"> is the most widely distributed amphibian species found in the Ryukyu Archipelago in Japan and Taiwan, and uses a wide range of breeding sites. Such characteristics suggest a high salinity and thermal tolerance in </span><em style="font-size: 12.16px;">B. japonica</em><span style="font-size: 12.16px;"> tadpoles. We measured the salinity and thermal tolerance of tadpoles from three islands to determine if physiological tolerance could have contributed to the wide dispersal and survival across different environments. The critical salinity of </span><em style="font-size: 12.16px;">B. japonica</em><span style="font-size: 12.16px;"> was 10–11‰, a value markedly below seawater. We also observed a critical maximum temperature of approximately 40°C, a value which is higher than what is commonly observed for other anuran species. This high thermal tolerance may have favoured island dispersal and survival, particularly in volcanic islands.</span></p>
<p class="MsoNormal">&nbsp;<strong>Key words:&nbsp;</strong>&nbsp;adaptation, geothermal hot springs, physiological tolerances, Ryukyu Archipelago, survival rate, Taiwan, volcanic islands</p>
<p><span style="font-size: 12.16px;"></span></p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/895-03-salinity-and-thermal-tolerance-of-japanese-stream-tree-frog-i-buergeria-japonica-i-tadpoles-from-island-populations?format=html</guid>
           <description><![CDATA[<p>pp. 207-211</p><p><em>Authors:&nbsp;</em>Shohei Komaki, Takeshi Igawa, Si-Min Lin &amp; Masayuki Sumida</p>
<p><span style="font-size: 12.16px;"><strong>Abstract:&nbsp;</strong></span><span style="font-size: 12.16px;">Physiological tolerance to variable environmental conditions is essential for species to disperse over habitat boundaries and sustain populations in new habitats. In particular, salinity and temperature are one of the major factors determining species’ distributions. The tree frog </span><em style="font-size: 12.16px;">Buergeria japonica</em><span style="font-size: 12.16px;"> is the most widely distributed amphibian species found in the Ryukyu Archipelago in Japan and Taiwan, and uses a wide range of breeding sites. Such characteristics suggest a high salinity and thermal tolerance in </span><em style="font-size: 12.16px;">B. japonica</em><span style="font-size: 12.16px;"> tadpoles. We measured the salinity and thermal tolerance of tadpoles from three islands to determine if physiological tolerance could have contributed to the wide dispersal and survival across different environments. The critical salinity of </span><em style="font-size: 12.16px;">B. japonica</em><span style="font-size: 12.16px;"> was 10–11‰, a value markedly below seawater. We also observed a critical maximum temperature of approximately 40°C, a value which is higher than what is commonly observed for other anuran species. This high thermal tolerance may have favoured island dispersal and survival, particularly in volcanic islands.</span></p>
<p class="MsoNormal">&nbsp;<strong>Key words:&nbsp;</strong>&nbsp;adaptation, geothermal hot springs, physiological tolerances, Ryukyu Archipelago, survival rate, Taiwan, volcanic islands</p>
<p><span style="font-size: 12.16px;"></span></p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
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              <item>
           <title>04. Does tail regeneration following autotomy restore lizard sprint speed? Evidence from the lacertid [i]Psammodromus algirus[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/896-04-does-tail-regeneration-following-autotomy-restore-lizard-sprint-speed-evidence-from-the-lacertid-i-psammodromus-algirus-i?format=html</link>
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           <media:title type="plain">04. Does tail regeneration following autotomy restore lizard sprint speed? Evidence from the lacertid [i]Psammodromus algirus[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp. 213-218</p><p><em>Authors:&nbsp;</em>Francisco Javier Zamora-Camacho, María Virtudes Rubiño-Hispán, Senda Reguera &amp; Gregorio Moreno-Rueda</p>
<p><strong>Abstract:&nbsp;</strong><span style="font-size: 12.16px;">Tail autotomy is a widespread antipredator strategy among lizards, which consists of the capability of willingly detaching a portion of the tail in order to escape predator attacks. Nonetheless, tail autotomy has a number of costs, including reduced sprint speed which increases predation risk. However, lizards regenerate the tail following autotomy, although a regenerated tail is usually shorter and histologically different from the original tail. In the present work, we assess the effect of tail regeneration on sprint speed by comparing </span><em style="font-size: 12.16px;">Psammodromus algirus</em><span style="font-size: 12.16px;"> lizards with intact and regenerated tails under controlled laboratory conditions. We found that sprint speed was similar in lizards with intact and regenerated tails. Therefore, tail regeneration following autotomy effectively restored sprint speed, although regenerated tails were shorter than intact ones. Thus, regenerating shorter tails could diminish anabolic costs with no negative consequences on flight ability.</span></p>
<p class="MsoNormal">&nbsp;<strong>Key words:</strong>&nbsp;intact tail, lizard, regenerated tail, sprint speed, tail autotomy</p>
<p><span style="font-size: 12.16px;"></span></p>
<p><span style="font-size: 12.16px;"></span></p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/896-04-does-tail-regeneration-following-autotomy-restore-lizard-sprint-speed-evidence-from-the-lacertid-i-psammodromus-algirus-i?format=html</guid>
           <description><![CDATA[<p>pp. 213-218</p><p><em>Authors:&nbsp;</em>Francisco Javier Zamora-Camacho, María Virtudes Rubiño-Hispán, Senda Reguera &amp; Gregorio Moreno-Rueda</p>
<p><strong>Abstract:&nbsp;</strong><span style="font-size: 12.16px;">Tail autotomy is a widespread antipredator strategy among lizards, which consists of the capability of willingly detaching a portion of the tail in order to escape predator attacks. Nonetheless, tail autotomy has a number of costs, including reduced sprint speed which increases predation risk. However, lizards regenerate the tail following autotomy, although a regenerated tail is usually shorter and histologically different from the original tail. In the present work, we assess the effect of tail regeneration on sprint speed by comparing </span><em style="font-size: 12.16px;">Psammodromus algirus</em><span style="font-size: 12.16px;"> lizards with intact and regenerated tails under controlled laboratory conditions. We found that sprint speed was similar in lizards with intact and regenerated tails. Therefore, tail regeneration following autotomy effectively restored sprint speed, although regenerated tails were shorter than intact ones. Thus, regenerating shorter tails could diminish anabolic costs with no negative consequences on flight ability.</span></p>
<p class="MsoNormal">&nbsp;<strong>Key words:</strong>&nbsp;intact tail, lizard, regenerated tail, sprint speed, tail autotomy</p>
<p><span style="font-size: 12.16px;"></span></p>
<p><span style="font-size: 12.16px;"></span></p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>04. Appendix</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/897-04-appendix?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/897-04-appendix/file" length="519609" type="application/pdf" />
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           <media:title type="plain">04. Appendix</media:title>
           <media:description type="html"><![CDATA[<p>Online appendix for&nbsp;04. Does tail regeneration following autotomy restore lizard sprint speed? Evidence from the lacertid <em>Psammodromus algirus</em></p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/897-04-appendix?format=html</guid>
           <description><![CDATA[<p>Online appendix for&nbsp;04. Does tail regeneration following autotomy restore lizard sprint speed? Evidence from the lacertid <em>Psammodromus algirus</em></p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>05. Geographic variation in advertisement calls among populations of [i]Dendropsophus cruzi[/i] (Anura: Hylidae)</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/898-05-geographic-variation-in-advertisement-calls-among-populations-of-i-dendropsophus-cruzi-i-anura-hylidae?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/898-05-geographic-variation-in-advertisement-calls-among-populations-of-i-dendropsophus-cruzi-i-anura-hylidae/file" length="1084786" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/898-05-geographic-variation-in-advertisement-calls-among-populations-of-i-dendropsophus-cruzi-i-anura-hylidae/file"
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           <media:title type="plain">05. Geographic variation in advertisement calls among populations of [i]Dendropsophus cruzi[/i] (Anura: Hylidae)</media:title>
           <media:description type="html"><![CDATA[<p>pp. 219-224</p><p><em>Authors:&nbsp;</em>Geiziane Tessarolo, Natan Medeiros Maciel, Alessandro Ribeiro Morais &amp; Rogério Pereira Bastos</p>
<p><strong>Abstract:&nbsp;</strong><span style="font-size: 12.16px;">Anuran advertisement calls receive much attention because of their importance in mating behaviour and the recognition of conspecifics. Herein, we studied geographic variation in the advertisement call of </span><em style="font-size: 12.16px;">Dendropsophus cruzi</em><span style="font-size: 12.16px;"> from central Brazil, to test the hypothesis that between-population differences in call parameters can be explained by geographical distance. We recorded 129 individuals from 10 populations of </span><em style="font-size: 12.16px;">D. cruzi</em><span style="font-size: 12.16px;"> in Goiás State, Brazil, measuring call parameters of five calls of each individual. We found that dominant frequency is useful to distinguish populations, and that geographic distance is not a predictor of overall call differences. However, clinal geographical patterns were found for call duration, dominant frequency, call rate and snout-vent length (SVL). We suggest that differences in calls among populations can be due to local selective pressures.</span></p>
<p class="MsoNormal">&nbsp;<strong>Key words:&nbsp;</strong>Anuran, dominant frequency, geographical patterns, isolation by distance</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/898-05-geographic-variation-in-advertisement-calls-among-populations-of-i-dendropsophus-cruzi-i-anura-hylidae?format=html</guid>
           <description><![CDATA[<p>pp. 219-224</p><p><em>Authors:&nbsp;</em>Geiziane Tessarolo, Natan Medeiros Maciel, Alessandro Ribeiro Morais &amp; Rogério Pereira Bastos</p>
<p><strong>Abstract:&nbsp;</strong><span style="font-size: 12.16px;">Anuran advertisement calls receive much attention because of their importance in mating behaviour and the recognition of conspecifics. Herein, we studied geographic variation in the advertisement call of </span><em style="font-size: 12.16px;">Dendropsophus cruzi</em><span style="font-size: 12.16px;"> from central Brazil, to test the hypothesis that between-population differences in call parameters can be explained by geographical distance. We recorded 129 individuals from 10 populations of </span><em style="font-size: 12.16px;">D. cruzi</em><span style="font-size: 12.16px;"> in Goiás State, Brazil, measuring call parameters of five calls of each individual. We found that dominant frequency is useful to distinguish populations, and that geographic distance is not a predictor of overall call differences. However, clinal geographical patterns were found for call duration, dominant frequency, call rate and snout-vent length (SVL). We suggest that differences in calls among populations can be due to local selective pressures.</span></p>
<p class="MsoNormal">&nbsp;<strong>Key words:&nbsp;</strong>Anuran, dominant frequency, geographical patterns, isolation by distance</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>05. Appendix</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/899-05-appendix?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/899-05-appendix/file" length="781052" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/899-05-appendix/file"
                fileSize="781052"
                type="application/pdf"
                medium="document"
           />
           <media:title type="plain">05. Appendix</media:title>
           <media:description type="html"><![CDATA[<p>Online appendix for&nbsp;05. Geographic variation in advertisement calls among populations of Dendropsophus cruzi (Anura: Hylidae)&nbsp;</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/899-05-appendix?format=html</guid>
           <description><![CDATA[<p>Online appendix for&nbsp;05. Geographic variation in advertisement calls among populations of Dendropsophus cruzi (Anura: Hylidae)&nbsp;</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>06. Sexual dimorphism and interspecific head variation in the [i]Liolaemus melanops[/i] complex (Squamata: Liolaemini) based on geometric morphometrics</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/900-06-sexual-dimorphism-and-interspecific-head-variation-in-the-i-liolaemus-melanops-i-complex-squamata-liolaemini-based-on-geometric-morphometrics?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/900-06-sexual-dimorphism-and-interspecific-head-variation-in-the-i-liolaemus-melanops-i-complex-squamata-liolaemini-based-on-geometric-morphometrics/file" length="2517496" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/900-06-sexual-dimorphism-and-interspecific-head-variation-in-the-i-liolaemus-melanops-i-complex-squamata-liolaemini-based-on-geometric-morphometrics/file"
                fileSize="2517496"
                type="application/pdf"
                medium="document"
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           <media:title type="plain">06. Sexual dimorphism and interspecific head variation in the [i]Liolaemus melanops[/i] complex (Squamata: Liolaemini) based on geometric morphometrics</media:title>
           <media:description type="html"><![CDATA[<p>pp. 225-235</p><p><em>Authors:&nbsp;</em>Ignacio Minoli, M. Morando &amp; Luciano J. Avila</p>
<p><strong>Abstract:&nbsp;</strong><span style="font-size: 12.16px;">By analysing size and shape separately, geometric morphometric methods (GM) are a powerful tool to evaluate morphological differences within and between taxa. In this work, we used GM to investigate whether lizards of the </span><em style="font-size: 12.16px;">Liolaemus melanops</em><span style="font-size: 12.16px;"> complex differ in shape and size. Specifically, we analysed head shape and size variation to quantify intraspecific sexual dimorphism and interspecific differences. We found sexual dimorphism in six of the seven investigated species (</span><em style="font-size: 12.16px;">L. canqueli, L. dumerili, L. goetschi, L. martorii, L. melanops </em><span style="font-size: 12.16px;">and</span><em style="font-size: 12.16px;"> L. morenoi</em><span style="font-size: 12.16px;">). Five species (</span><em style="font-size: 12.16px;">L. canqueli, L. casamiquelai, L. martorii, L. melanops </em><span style="font-size: 12.16px;">and</span><em style="font-size: 12.16px;"> L. morenoi</em><span style="font-size: 12.16px;">) were distinct in shape and size, </span><em style="font-size: 12.16px;">whereas L. goetschi </em><span style="font-size: 12.16px;">and</span><em style="font-size: 12.16px;"> L. dumerili</em><span style="font-size: 12.16px;"> were indiscernible from each other. This work illustrates the value of GM to study morphological variation in lizards, suggesting that similar studies would be valuable for testing species boundaries in other groups of </span><em style="font-size: 12.16px;">Liolaemus</em><span style="font-size: 12.16px;">.</span></p>
<p><strong>Key words:</strong>&nbsp;Lizards, Liolaemus, morphological diversity, species' boundaries</p>
<p><span style="font-size: 12.16px;"></span></p>
<p class="MsoNormal">&nbsp;</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/900-06-sexual-dimorphism-and-interspecific-head-variation-in-the-i-liolaemus-melanops-i-complex-squamata-liolaemini-based-on-geometric-morphometrics?format=html</guid>
           <description><![CDATA[<p>pp. 225-235</p><p><em>Authors:&nbsp;</em>Ignacio Minoli, M. Morando &amp; Luciano J. Avila</p>
<p><strong>Abstract:&nbsp;</strong><span style="font-size: 12.16px;">By analysing size and shape separately, geometric morphometric methods (GM) are a powerful tool to evaluate morphological differences within and between taxa. In this work, we used GM to investigate whether lizards of the </span><em style="font-size: 12.16px;">Liolaemus melanops</em><span style="font-size: 12.16px;"> complex differ in shape and size. Specifically, we analysed head shape and size variation to quantify intraspecific sexual dimorphism and interspecific differences. We found sexual dimorphism in six of the seven investigated species (</span><em style="font-size: 12.16px;">L. canqueli, L. dumerili, L. goetschi, L. martorii, L. melanops </em><span style="font-size: 12.16px;">and</span><em style="font-size: 12.16px;"> L. morenoi</em><span style="font-size: 12.16px;">). Five species (</span><em style="font-size: 12.16px;">L. canqueli, L. casamiquelai, L. martorii, L. melanops </em><span style="font-size: 12.16px;">and</span><em style="font-size: 12.16px;"> L. morenoi</em><span style="font-size: 12.16px;">) were distinct in shape and size, </span><em style="font-size: 12.16px;">whereas L. goetschi </em><span style="font-size: 12.16px;">and</span><em style="font-size: 12.16px;"> L. dumerili</em><span style="font-size: 12.16px;"> were indiscernible from each other. This work illustrates the value of GM to study morphological variation in lizards, suggesting that similar studies would be valuable for testing species boundaries in other groups of </span><em style="font-size: 12.16px;">Liolaemus</em><span style="font-size: 12.16px;">.</span></p>
<p><strong>Key words:</strong>&nbsp;Lizards, Liolaemus, morphological diversity, species' boundaries</p>
<p><span style="font-size: 12.16px;"></span></p>
<p class="MsoNormal">&nbsp;</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>06. Appendix</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/901-06-appendix-1?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/901-06-appendix-1/file" length="3342218" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/901-06-appendix-1/file"
                fileSize="3342218"
                type="application/pdf"
                medium="document"
           />
           <media:title type="plain">06. Appendix</media:title>
           <media:description type="html"><![CDATA[<p>Online appendix for&nbsp;06. Sexual dimorphism and interspecific head variation in the <em>Liolaemus melanops</em> complex (Squamata: Liolaemini) based on geometric morphometrics</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/901-06-appendix-1?format=html</guid>
           <description><![CDATA[<p>Online appendix for&nbsp;06. Sexual dimorphism and interspecific head variation in the <em>Liolaemus melanops</em> complex (Squamata: Liolaemini) based on geometric morphometrics</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>07. Escalated antipredator mechanisms of two neotropical marsupial treefrogs</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/902-07-escalated-antipredator-mechanisms-of-two-neotropical-marsupial-treefrogs?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/902-07-escalated-antipredator-mechanisms-of-two-neotropical-marsupial-treefrogs/file" length="21185213" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/902-07-escalated-antipredator-mechanisms-of-two-neotropical-marsupial-treefrogs/file"
                fileSize="21185213"
                type="application/pdf"
                medium="document"
           />
           <media:title type="plain">07. Escalated antipredator mechanisms of two neotropical marsupial treefrogs</media:title>
           <media:description type="html"><![CDATA[<div>pp. 237-244</div><div>&nbsp;</div>
<div><em>Authors:&nbsp;</em>Ricardo Lourenço-de-Moraes, Rodrigo B. Ferreira, Caio V. Mira-Mendes, Cassio Z. Zocca, Tadeu Medeiros, Danilo S. Ruas, Raoni Rebouças, Luís Felipe Toledo, Edmund D. Brodie Jr. &amp; Mirco Solé</div>
<div>&nbsp;</div>
<div><strong>Abstract:&nbsp;</strong>The sequence and intensity of antipredator mechanisms may be displayed according to the risk of predation. We tested this hypothesis using two species of marsupial treefrogs from Brazil’s Atlantic Forest. We observed <em>Gastrotheca recava</em> and <em>G. megacephala</em> displaying nine antipredator mechanisms and three types of defensive calls. These behaviours were displayed in an escalated sequence from motionless (passive behaviour) to biting (the most aggressive behaviour). This diversified set of antipredator mechanisms may be related to the interaction between predator and prey at the local scale. The escalated sequence of defensive behaviours should be considered in future studies on anuran-predator interaction.</div>
<div>&nbsp;</div>
<div><strong>Key words:&nbsp;&nbsp;</strong>Amphibia, Atlantic forest, defensive behaviour, defensive call, <em>Gastrotheca</em>, Hemiphractidae</div>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/902-07-escalated-antipredator-mechanisms-of-two-neotropical-marsupial-treefrogs?format=html</guid>
           <description><![CDATA[<div>pp. 237-244</div><div>&nbsp;</div>
<div><em>Authors:&nbsp;</em>Ricardo Lourenço-de-Moraes, Rodrigo B. Ferreira, Caio V. Mira-Mendes, Cassio Z. Zocca, Tadeu Medeiros, Danilo S. Ruas, Raoni Rebouças, Luís Felipe Toledo, Edmund D. Brodie Jr. &amp; Mirco Solé</div>
<div>&nbsp;</div>
<div><strong>Abstract:&nbsp;</strong>The sequence and intensity of antipredator mechanisms may be displayed according to the risk of predation. We tested this hypothesis using two species of marsupial treefrogs from Brazil’s Atlantic Forest. We observed <em>Gastrotheca recava</em> and <em>G. megacephala</em> displaying nine antipredator mechanisms and three types of defensive calls. These behaviours were displayed in an escalated sequence from motionless (passive behaviour) to biting (the most aggressive behaviour). This diversified set of antipredator mechanisms may be related to the interaction between predator and prey at the local scale. The escalated sequence of defensive behaviours should be considered in future studies on anuran-predator interaction.</div>
<div>&nbsp;</div>
<div><strong>Key words:&nbsp;&nbsp;</strong>Amphibia, Atlantic forest, defensive behaviour, defensive call, <em>Gastrotheca</em>, Hemiphractidae</div>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>08. Spawning location is linked to the relative size of olfactory nerves in anurans</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/905-08-spawning-location-is-linked-to-the-relative-size-of-olfactory-nerves-in-anurans?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/905-08-spawning-location-is-linked-to-the-relative-size-of-olfactory-nerves-in-anurans/file" length="1796008" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/905-08-spawning-location-is-linked-to-the-relative-size-of-olfactory-nerves-in-anurans/file"
                fileSize="1796008"
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                medium="document"
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           <media:title type="plain">08. Spawning location is linked to the relative size of olfactory nerves in anurans</media:title>
           <media:description type="html"><![CDATA[<p class="MsoNormal">pp. 245-248</p><p>&nbsp;</p>
<p class="MsoNormal"><em>Authors: </em>Qing Gui Wu, Shang Ling Lou, Yu Zeng &amp; Wen Bo Liao</p>
<p class="MsoNormal"><strong>Abstract: </strong>The brain is the most important organ associated with demands on cognitive ability, and selection pressures have been implicated to explain variation in brain size and brain architecture in a wide range of taxa. Using phylogenetic comparative methods, we studied the effect of spawning location (terrestrial, lentic and lotic) on variation in the size of different brain parts among 43 Chinese anuran species. Spawning location was not significantly associated with relative brain size, and there were no links between spawning location and independent contrasts in size of the olfactory bulbs, telencephalon, optic tecta and cerebellum. However, the independent contrasts in size of the olfactory nerves differed significantly among the three types of spawning location. Our findings provide evidence that the brain structures underlying olfaction are linked to life history attributes required for spawning in specific habitat types.</p>
<p class="MsoNormal"><strong>Key words: </strong>anurans, comparative method, olfactory nerves, spawning location</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/905-08-spawning-location-is-linked-to-the-relative-size-of-olfactory-nerves-in-anurans?format=html</guid>
           <description><![CDATA[<p class="MsoNormal">pp. 245-248</p><p>&nbsp;</p>
<p class="MsoNormal"><em>Authors: </em>Qing Gui Wu, Shang Ling Lou, Yu Zeng &amp; Wen Bo Liao</p>
<p class="MsoNormal"><strong>Abstract: </strong>The brain is the most important organ associated with demands on cognitive ability, and selection pressures have been implicated to explain variation in brain size and brain architecture in a wide range of taxa. Using phylogenetic comparative methods, we studied the effect of spawning location (terrestrial, lentic and lotic) on variation in the size of different brain parts among 43 Chinese anuran species. Spawning location was not significantly associated with relative brain size, and there were no links between spawning location and independent contrasts in size of the olfactory bulbs, telencephalon, optic tecta and cerebellum. However, the independent contrasts in size of the olfactory nerves differed significantly among the three types of spawning location. Our findings provide evidence that the brain structures underlying olfaction are linked to life history attributes required for spawning in specific habitat types.</p>
<p class="MsoNormal"><strong>Key words: </strong>anurans, comparative method, olfactory nerves, spawning location</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>08. Appendix</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/907-08-appendix-1?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/907-08-appendix-1/file" length="799664" type="application/pdf" />
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                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/907-08-appendix-1/file"
                fileSize="799664"
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                medium="document"
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           <media:title type="plain">08. Appendix</media:title>
           <media:description type="html"><![CDATA[<p>Online appendix for&nbsp;<span style="font-size: 12.16px;">08. Spawning location is linked to the relative size of olfactory nerves in anurans</span></p><p class="MsoNormal">&nbsp;</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/907-08-appendix-1?format=html</guid>
           <description><![CDATA[<p>Online appendix for&nbsp;<span style="font-size: 12.16px;">08. Spawning location is linked to the relative size of olfactory nerves in anurans</span></p><p class="MsoNormal">&nbsp;</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>09. A comparison of testes size and sperm length between [i]Polypedates megacephalus[/i] populations at different altitudes</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/908-09-a-comparison-of-testes-size-and-sperm-length-between-i-polypedates-megacephalus-i-populations-at-different-altitudes?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/908-09-a-comparison-of-testes-size-and-sperm-length-between-i-polypedates-megacephalus-i-populations-at-different-altitudes/file" length="622079" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/908-09-a-comparison-of-testes-size-and-sperm-length-between-i-polypedates-megacephalus-i-populations-at-different-altitudes/file"
                fileSize="622079"
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           <media:title type="plain">09. A comparison of testes size and sperm length between [i]Polypedates megacephalus[/i] populations at different altitudes</media:title>
           <media:description type="html"><![CDATA[<p class="MsoNormal">pp. 249-252</p><p class="MsoNormal"><em>Authors: </em>Cheng Chen, You You Huang &amp; Wen Bo Liao</p>
<p class="MsoNormal"><strong>Abstract: </strong>Variation in temperature and breeding season length caused by altitude has long been considered a major influence on the evolution of life-history traits in amphibians. Here, we examined differences in reproductive investment (testes mass and sperm length) of male spot-legged treefrog (<em>Polypedates megacephalus</em>) from two altitudes (680 m and 1300 m above sea level) in Guizhou Province, western China. Relative testes size from the high-altitude population was larger than that of the low-altitude population, whereas sperm length exhibited a converse cline. Testes mass but not sperm length increased with body size at both altitudes. Our findings suggest that differences in reproductive traits between populations might result from differences in the level of sperm competition.</p>
<p>&nbsp;</p>
<p class="MsoNormal"><strong>Key words: </strong>Altitude, life history, <em>Polypedates megacephalus</em>, sperm length, testes size</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/908-09-a-comparison-of-testes-size-and-sperm-length-between-i-polypedates-megacephalus-i-populations-at-different-altitudes?format=html</guid>
           <description><![CDATA[<p class="MsoNormal">pp. 249-252</p><p class="MsoNormal"><em>Authors: </em>Cheng Chen, You You Huang &amp; Wen Bo Liao</p>
<p class="MsoNormal"><strong>Abstract: </strong>Variation in temperature and breeding season length caused by altitude has long been considered a major influence on the evolution of life-history traits in amphibians. Here, we examined differences in reproductive investment (testes mass and sperm length) of male spot-legged treefrog (<em>Polypedates megacephalus</em>) from two altitudes (680 m and 1300 m above sea level) in Guizhou Province, western China. Relative testes size from the high-altitude population was larger than that of the low-altitude population, whereas sperm length exhibited a converse cline. Testes mass but not sperm length increased with body size at both altitudes. Our findings suggest that differences in reproductive traits between populations might result from differences in the level of sperm competition.</p>
<p>&nbsp;</p>
<p class="MsoNormal"><strong>Key words: </strong>Altitude, life history, <em>Polypedates megacephalus</em>, sperm length, testes size</p>]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
       </item>
              <item>
           <title>Front Cover</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/910-front-cover-3?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/910-front-cover-3/file" length="8271141" type="image/png" />
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                medium="image"
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           <media:title type="plain">Front Cover</media:title>
           <media:description type="html"><![CDATA[]]></media:description>
                      <media:thumbnail url="https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/910-front-cover-3/file" />
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-26-number-3-july-2016/910-front-cover-3?format=html</guid>
           <description><![CDATA[]]></description>
           <author>avonplettenberglaing@gmail.com (Anthony von Plettenberg Laing)</author>
           <category>Volume 26, Number 3, July 2016</category>
           <pubDate>Fri, 29 Jul 2016 00:00:00 +0100</pubDate>
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