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       <title>Volume 27, Number 4, October 2017 - British Herpetological Society</title>
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           <title>Volume 27, Number 4, October 2017 - British Herpetological Society</title>
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           <title>Front cover 27(4)</title>
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           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Mon, 09 Oct 2017 15:28:16 +0100</pubDate>
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           <title>27(4) inside cover</title>
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           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:38:05 +0100</pubDate>
       </item>
              <item>
           <title>Online appendix for 05. Tadpole species richness within lentic and lotic microhabitats: an interactive influence of environmental and spatial factors</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1060-online-appendix-for-05-tadpole-species-richness-within-lentic-and-lotic-microhabitats-an-interactive-influence-of-environmental-and-spatial-factors?format=html</link>
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           <media:title type="plain">Online appendix for 05. Tadpole species richness within lentic and lotic microhabitats: an interactive influence of environmental and spatial factors</media:title>
           <media:description type="html"><![CDATA[<p>pp. 339-345</p>
<p><strong>Authors</strong>: Lilian Sayuri Ouchi de Melo, Thiago Gonçalves-Souza, Michel Varajão Garey &amp; Denise de Cerqueira</p>]]></media:description>
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           <description><![CDATA[<p>pp. 339-345</p>
<p><strong>Authors</strong>: Lilian Sayuri Ouchi de Melo, Thiago Gonçalves-Souza, Michel Varajão Garey &amp; Denise de Cerqueira</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:38:05 +0100</pubDate>
       </item>
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           <title>27(4) back cover</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1058-27-4-back-cover?format=html</link>
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           <media:title type="plain">27(4) back cover</media:title>
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           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:38:04 +0100</pubDate>
       </item>
              <item>
           <title>Volume 27, Number 4, October 2017 - Full Issue</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1057-volume-27-number-4-october-2017-full-issue?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1057-volume-27-number-4-october-2017-full-issue/file" length="5242316" type="application/pdf" />
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           <media:title type="plain">Volume 27, Number 4, October 2017 - Full Issue</media:title>
           <media:description type="html"><![CDATA[<p>pp. 307-378</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1057-volume-27-number-4-october-2017-full-issue?format=html</guid>
           <description><![CDATA[<p>pp. 307-378</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:38:03 +0100</pubDate>
       </item>
              <item>
           <title>08. Frogs in pre-industrial Britain</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1056-08-frogs-in-pre-industrial-britain?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1056-08-frogs-in-pre-industrial-britain/file" length="1571305" type="application/pdf" />
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           <media:title type="plain">08. Frogs in pre-industrial Britain</media:title>
           <media:description type="html"><![CDATA[<p>pp. 368-378</p>
<p><strong>Authors</strong>: Lee Raye</p>
<p><strong>Abstract</strong>: This paper examines the pre-industrial historical record of Britain’s anuran species. The records examined include especially<br />the writings of naturalists and physicians, most notably Gerald of Wales (1188), John of Gaddesden (c.1314), Edward Wotton<br />(1552), Timothie Bright (1580), Thomas Brown (1646), Robert Lovell (1660), Christopher Merrett (1667), Robert Sibbald (1684)<br />and John Morton (1712). The common frog is attested as present throughout the period. Several reliable historical records<br />are located that describe the presence or absence of a water frog species ([i]Peloyphylax[/i] spp.: two records of presence, two of<br />absence) and the tree frog ([i]Hyla arborea[/i]: five records of presence, three of absence). The moor frog (Rana arvalis) and agile<br />frog ([i]Rana dalmatina[/i]) are not described separately – if present in the time period, they may have been considered varieties<br />of the common frog. The evidence of presence comes exclusively from England. The records taken together confirm the<br />presence of populations of water frogs between (at least) the fifteenth and eighteenth century, and provide new evidence<br />attesting to populations of tree frogs between the sixteenth century (when the species may have been introduced) and the<br />eighteenth century (when the species seems to have become locally extinct/locally distributed).</p>
<p><strong>Keywords</strong>: pool frog, tree frog, native status, species history, historical analysis</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1056-08-frogs-in-pre-industrial-britain?format=html</guid>
           <description><![CDATA[<p>pp. 368-378</p>
<p><strong>Authors</strong>: Lee Raye</p>
<p><strong>Abstract</strong>: This paper examines the pre-industrial historical record of Britain’s anuran species. The records examined include especially<br />the writings of naturalists and physicians, most notably Gerald of Wales (1188), John of Gaddesden (c.1314), Edward Wotton<br />(1552), Timothie Bright (1580), Thomas Brown (1646), Robert Lovell (1660), Christopher Merrett (1667), Robert Sibbald (1684)<br />and John Morton (1712). The common frog is attested as present throughout the period. Several reliable historical records<br />are located that describe the presence or absence of a water frog species ([i]Peloyphylax[/i] spp.: two records of presence, two of<br />absence) and the tree frog ([i]Hyla arborea[/i]: five records of presence, three of absence). The moor frog (Rana arvalis) and agile<br />frog ([i]Rana dalmatina[/i]) are not described separately – if present in the time period, they may have been considered varieties<br />of the common frog. The evidence of presence comes exclusively from England. The records taken together confirm the<br />presence of populations of water frogs between (at least) the fifteenth and eighteenth century, and provide new evidence<br />attesting to populations of tree frogs between the sixteenth century (when the species may have been introduced) and the<br />eighteenth century (when the species seems to have become locally extinct/locally distributed).</p>
<p><strong>Keywords</strong>: pool frog, tree frog, native status, species history, historical analysis</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:38:02 +0100</pubDate>
       </item>
              <item>
           <title>07. The trade of [i]Kinosternon scorpioides[/i] on Marajó island, Brazilian Amazon: from hunting to consumption</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1055-07-the-trade-of-i-kinosternon-scorpioides-i-on-marajo-island-brazilian-amazon-from-hunting-to-consumption?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1055-07-the-trade-of-i-kinosternon-scorpioides-i-on-marajo-island-brazilian-amazon-from-hunting-to-consumption/file" length="1828109" type="application/pdf" />
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           <media:title type="plain">07. The trade of [i]Kinosternon scorpioides[/i] on Marajó island, Brazilian Amazon: from hunting to consumption</media:title>
           <media:description type="html"><![CDATA[<p>pp. 361-367</p>
<p><strong>Authors</strong>: Samuel Silva de Cristo, Pedro Chaves Baía Júnior, Joilson Silva da Silva, José Ribamar Felipe<br />Marques &amp; Diva Anelie de Araújo Guimarães</p>
<p><strong>Abstract</strong>: We studied the trade network of the Scorpion Mud Turtle, [i]Kinosternon scorpioides[/i], on Marajó Island, Brazil, from hunting to<br />the final product consumption. We conducted semi-structured interviews at the urban centers of the cities of Soure, Salvaterra<br />and Cachoeira do Arari, where we investigated: A) the socioeconomic profile of the merchants and their activity; B) the origin,<br />form and the frequency of marketing [i]K. scorpioides[/i]; and C) the demand for the product. Scorpion Mud Turtle hunting was<br />carried out using the following methods: hand-collection (100%), probing (62%) and burning (54%). They were hunted for two<br />reasons: personal consumption and sale, which was conducted in urban centers. The hunters knew the empirical aspects of the<br />species biology in the wild: habitat, trophic ecology, and reproduction, among others. The trade of [i]K. scorpioides[/i] is still a strong<br />activity on Marajó Island, and the legal regulations are not enough to inhibit this practice, which poses a threat to the future of<br />this species in this area. The establishment of educational efforts and captive breeding programs of this species will contribute<br />to employment, to local family income, and to the conservation of this genetic resource. These efforts also be important for<br />that the local population could produce and consume this species in a more sustainable way.</p>
<p><strong>Keywords</strong>: biodiversity; ethnobiology; scorpion mud turtle; chelonians</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1055-07-the-trade-of-i-kinosternon-scorpioides-i-on-marajo-island-brazilian-amazon-from-hunting-to-consumption?format=html</guid>
           <description><![CDATA[<p>pp. 361-367</p>
<p><strong>Authors</strong>: Samuel Silva de Cristo, Pedro Chaves Baía Júnior, Joilson Silva da Silva, José Ribamar Felipe<br />Marques &amp; Diva Anelie de Araújo Guimarães</p>
<p><strong>Abstract</strong>: We studied the trade network of the Scorpion Mud Turtle, [i]Kinosternon scorpioides[/i], on Marajó Island, Brazil, from hunting to<br />the final product consumption. We conducted semi-structured interviews at the urban centers of the cities of Soure, Salvaterra<br />and Cachoeira do Arari, where we investigated: A) the socioeconomic profile of the merchants and their activity; B) the origin,<br />form and the frequency of marketing [i]K. scorpioides[/i]; and C) the demand for the product. Scorpion Mud Turtle hunting was<br />carried out using the following methods: hand-collection (100%), probing (62%) and burning (54%). They were hunted for two<br />reasons: personal consumption and sale, which was conducted in urban centers. The hunters knew the empirical aspects of the<br />species biology in the wild: habitat, trophic ecology, and reproduction, among others. The trade of [i]K. scorpioides[/i] is still a strong<br />activity on Marajó Island, and the legal regulations are not enough to inhibit this practice, which poses a threat to the future of<br />this species in this area. The establishment of educational efforts and captive breeding programs of this species will contribute<br />to employment, to local family income, and to the conservation of this genetic resource. These efforts also be important for<br />that the local population could produce and consume this species in a more sustainable way.</p>
<p><strong>Keywords</strong>: biodiversity; ethnobiology; scorpion mud turtle; chelonians</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:38:01 +0100</pubDate>
       </item>
              <item>
           <title>06. Evolutionary patterns in life-history traits of lizards of the genus [i]Xenosaurus[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1054-06-evolutionary-patterns-in-life-history-traits-of-lizards-of-the-genus-i-xenosaurus-i?format=html</link>
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           <media:title type="plain">06. Evolutionary patterns in life-history traits of lizards of the genus [i]Xenosaurus[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp. 346-360</p>
<p><strong>Authors</strong>: J. Jaime Zúñiga-Vega, Jesualdo A. Fuentes-G., J. Gastón Zamora-Abrego, Uri O. García-<br />Vázquez, Adrián Nieto-Montes de Oca &amp; Emília P. Martins</p>
<p><strong>Abstract</strong>: Life histories are directly related to fitness and, hence, are the focus of strong selective pressures. However, different life-history<br />traits may evolve at different paces and may respond differentially to particular selective pressures. We examined patterns<br />of evolutionary change in the following life-history traits of xenosaurid lizards: size at maturity, average size of adult females,<br />litter size, neonate size, and relative litter mass. We used a phylogenetic hypothesis of the genus <em>Xenosaurus</em> and different<br />phylogenetic comparative methods to search for evolutionary relationships between traits as well as to estimate ancestral<br />states, rates of evolution, and the amount of phylogenetic signal on each trait. In addition, we searched for differences in<br />these life-history traits among the different environments where these lizards inhabit (cloud forest, tropical forest, oak-pine<br />forest, and xeric scrub). We found an evolutionary relationship between size at maturity and average adult size, with larger<br />species maturing at larger sizes. We also found an evolutionary trade-off between litter size and neonate size. Ancestral state<br />reconstructions revealed differences among traits in the relative timing of diversification. Litter size and neonate size began<br />diversification early in the history of the genus. In contrast, size at maturity and relative litter mass remained phenotypically<br />invariant for a long time period before diverging into distinct phenotypic values. Litter size exhibited significant phylogenetic<br />signal because the diversification history of this trait has tracked the phylogeny closely. The observed variation among species<br />in neonate size also showed some trace of the phylogenetic relationships. The remaining three traits diverged throughout time<br />without a clear phylogenetic pattern. In addition, litter size and relative litter mass exhibited the highest evolutionary rates<br />whereas average adult size and neonate size exhibited the lowest rates. Litter size was the only trait that differed significantly<br />among environments, with largest litters in cloud forests. We discuss potential hypotheses to explain the observed differences<br />among life-history traits in the tempo and mode of evolution.</p>
<p><strong>Keywords</strong>: ancestral state reconstructions, evolutionary rates, life histories, phylogenetic signal, trade-offs, xenosaurid lizards</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1054-06-evolutionary-patterns-in-life-history-traits-of-lizards-of-the-genus-i-xenosaurus-i?format=html</guid>
           <description><![CDATA[<p>pp. 346-360</p>
<p><strong>Authors</strong>: J. Jaime Zúñiga-Vega, Jesualdo A. Fuentes-G., J. Gastón Zamora-Abrego, Uri O. García-<br />Vázquez, Adrián Nieto-Montes de Oca &amp; Emília P. Martins</p>
<p><strong>Abstract</strong>: Life histories are directly related to fitness and, hence, are the focus of strong selective pressures. However, different life-history<br />traits may evolve at different paces and may respond differentially to particular selective pressures. We examined patterns<br />of evolutionary change in the following life-history traits of xenosaurid lizards: size at maturity, average size of adult females,<br />litter size, neonate size, and relative litter mass. We used a phylogenetic hypothesis of the genus <em>Xenosaurus</em> and different<br />phylogenetic comparative methods to search for evolutionary relationships between traits as well as to estimate ancestral<br />states, rates of evolution, and the amount of phylogenetic signal on each trait. In addition, we searched for differences in<br />these life-history traits among the different environments where these lizards inhabit (cloud forest, tropical forest, oak-pine<br />forest, and xeric scrub). We found an evolutionary relationship between size at maturity and average adult size, with larger<br />species maturing at larger sizes. We also found an evolutionary trade-off between litter size and neonate size. Ancestral state<br />reconstructions revealed differences among traits in the relative timing of diversification. Litter size and neonate size began<br />diversification early in the history of the genus. In contrast, size at maturity and relative litter mass remained phenotypically<br />invariant for a long time period before diverging into distinct phenotypic values. Litter size exhibited significant phylogenetic<br />signal because the diversification history of this trait has tracked the phylogeny closely. The observed variation among species<br />in neonate size also showed some trace of the phylogenetic relationships. The remaining three traits diverged throughout time<br />without a clear phylogenetic pattern. In addition, litter size and relative litter mass exhibited the highest evolutionary rates<br />whereas average adult size and neonate size exhibited the lowest rates. Litter size was the only trait that differed significantly<br />among environments, with largest litters in cloud forests. We discuss potential hypotheses to explain the observed differences<br />among life-history traits in the tempo and mode of evolution.</p>
<p><strong>Keywords</strong>: ancestral state reconstructions, evolutionary rates, life histories, phylogenetic signal, trade-offs, xenosaurid lizards</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:38:00 +0100</pubDate>
       </item>
              <item>
           <title>05. Tadpole species richness within lentic and lotic microhabitats: an interactive influence of environmental and spatial factors</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1053-05-tadpole-species-richness-within-lentic-and-lotic-microhabitats-an-interactive-influence-of-environmental-and-spatial-factors?format=html</link>
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           <media:title type="plain">05. Tadpole species richness within lentic and lotic microhabitats: an interactive influence of environmental and spatial factors</media:title>
           <media:description type="html"><![CDATA[<p>pp. 339-345</p>
<p><strong>Authors</strong>: Lilian Sayuri Ouchi de Melo, Thiago Gonçalves-Souza, Michel Varajão Garey &amp; Denise de<br />Cerqueira</p>
<p><strong>Abstract</strong>: Anurans inhabiting lentic and lotic water bodies show distinct responses to environmental and spatial variables due to dispersal<br />by adults and microhabitat selection by tadpoles, which creates a hierarchical structure in these metacommunities. Aiming to<br />understand the influence of tadpole microhabitat selection and adult dispersal on species richness distribution, we tested the<br />influence of microhabitat environmental variables and habitat spatial variables on tadpole richness in lentic and lotic water<br />bodies located in the Atlantic Rainforest. We sampled tadpoles in 99 lentic microhabitats and 288 lotic microhabitats for<br />seven months. We performed a Hierarchical Partitioning Analysis to test the influence of environmental and spatial variables.<br />The percentage of aquatic vegetation within microhabitats and the main spatial gradient (dbMEM1) affected species richness<br />in lentic water bodies. Sand percentage, aquatic vegetation, and depth in the microhabitat and small-scale spatial gradient<br />(dbMEM4) affected species richness in lotic water bodies. Spatial processes indicate an influence of adult dispersal limitation<br />in search of reproductive habitats. The influence of microhabitat variables was mostly related to the amount of aquatic<br />vegetation, indicating the influence of environmental processes on the larval phase of anuran life cycle. In conclusion, both<br />environmental and spatial processes are driving the species richness in microhabitats inside lentic and lotic water bodies in<br />the Atlantic Rainforest.</p>
<p><strong>Keywords</strong>: Amphibians; biodiversity hotspot; microhabitat; species number; Tropical Rainforest</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1053-05-tadpole-species-richness-within-lentic-and-lotic-microhabitats-an-interactive-influence-of-environmental-and-spatial-factors?format=html</guid>
           <description><![CDATA[<p>pp. 339-345</p>
<p><strong>Authors</strong>: Lilian Sayuri Ouchi de Melo, Thiago Gonçalves-Souza, Michel Varajão Garey &amp; Denise de<br />Cerqueira</p>
<p><strong>Abstract</strong>: Anurans inhabiting lentic and lotic water bodies show distinct responses to environmental and spatial variables due to dispersal<br />by adults and microhabitat selection by tadpoles, which creates a hierarchical structure in these metacommunities. Aiming to<br />understand the influence of tadpole microhabitat selection and adult dispersal on species richness distribution, we tested the<br />influence of microhabitat environmental variables and habitat spatial variables on tadpole richness in lentic and lotic water<br />bodies located in the Atlantic Rainforest. We sampled tadpoles in 99 lentic microhabitats and 288 lotic microhabitats for<br />seven months. We performed a Hierarchical Partitioning Analysis to test the influence of environmental and spatial variables.<br />The percentage of aquatic vegetation within microhabitats and the main spatial gradient (dbMEM1) affected species richness<br />in lentic water bodies. Sand percentage, aquatic vegetation, and depth in the microhabitat and small-scale spatial gradient<br />(dbMEM4) affected species richness in lotic water bodies. Spatial processes indicate an influence of adult dispersal limitation<br />in search of reproductive habitats. The influence of microhabitat variables was mostly related to the amount of aquatic<br />vegetation, indicating the influence of environmental processes on the larval phase of anuran life cycle. In conclusion, both<br />environmental and spatial processes are driving the species richness in microhabitats inside lentic and lotic water bodies in<br />the Atlantic Rainforest.</p>
<p><strong>Keywords</strong>: Amphibians; biodiversity hotspot; microhabitat; species number; Tropical Rainforest</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:37:59 +0100</pubDate>
       </item>
              <item>
           <title>04. Social spacing of the montane lizard [i]Tropidurus montanus[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1052-04-social-spacing-of-the-montane-lizard-i-tropidurus-montanus-i?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1052-04-social-spacing-of-the-montane-lizard-i-tropidurus-montanus-i/file" length="1367575" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1052-04-social-spacing-of-the-montane-lizard-i-tropidurus-montanus-i/file"
                fileSize="1367575"
                type="application/pdf"
                medium="document"
           />
           <media:title type="plain">04. Social spacing of the montane lizard [i]Tropidurus montanus[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp. 333-338</p>
<p><strong>Authors</strong>: Conrado A. B. Galdino Stefania P. R. Ventura, Clara Cabral Lisboa &amp; Robert J. Young</p>
<p><strong>Abstract</strong>: The way in which individuals use their surrounding space can be key to understanding species’ sociobiology. We studied the<br />social spacing of the lizard <em>Tropidurus montanus</em>. Males were found to have larger home ranges than females. Male body<br />size was not associated with home range area, and the number of females associated with a male’s home range was small<br />when compared to other Iguanian lizards, thus forming small harems. The larger home range areas and overlaps found during<br />the final period of the reproductive season might occur as a consequence of reduced social interactions at the end of the<br />reproductive season. We provide evidence that the tropidurid <em>T. montanus</em> may be establishing short-term exclusive-use areas.</p>
<p><strong>Keywords</strong>: Home range, site fidelity, space use, Tropiduridade</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1052-04-social-spacing-of-the-montane-lizard-i-tropidurus-montanus-i?format=html</guid>
           <description><![CDATA[<p>pp. 333-338</p>
<p><strong>Authors</strong>: Conrado A. B. Galdino Stefania P. R. Ventura, Clara Cabral Lisboa &amp; Robert J. Young</p>
<p><strong>Abstract</strong>: The way in which individuals use their surrounding space can be key to understanding species’ sociobiology. We studied the<br />social spacing of the lizard <em>Tropidurus montanus</em>. Males were found to have larger home ranges than females. Male body<br />size was not associated with home range area, and the number of females associated with a male’s home range was small<br />when compared to other Iguanian lizards, thus forming small harems. The larger home range areas and overlaps found during<br />the final period of the reproductive season might occur as a consequence of reduced social interactions at the end of the<br />reproductive season. We provide evidence that the tropidurid <em>T. montanus</em> may be establishing short-term exclusive-use areas.</p>
<p><strong>Keywords</strong>: Home range, site fidelity, space use, Tropiduridade</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:37:58 +0100</pubDate>
       </item>
              <item>
           <title>03. Effects of Chinese tallow leaf litter on water chemistry and surfacing behaviour of anuran larvae</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1051-03-effects-of-chinese-tallow-leaf-litter-on-water-chemistry-and-surfacing-behaviour-of-anuran-larvae?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1051-03-effects-of-chinese-tallow-leaf-litter-on-water-chemistry-and-surfacing-behaviour-of-anuran-larvae/file" length="1390427" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1051-03-effects-of-chinese-tallow-leaf-litter-on-water-chemistry-and-surfacing-behaviour-of-anuran-larvae/file"
                fileSize="1390427"
                type="application/pdf"
                medium="document"
           />
           <media:title type="plain">03. Effects of Chinese tallow leaf litter on water chemistry and surfacing behaviour of anuran larvae</media:title>
           <media:description type="html"><![CDATA[<p>pp. 326-332</p>
<p><strong>Authors</strong>: Daniel Saenz &amp; Cory K. Adams</p>
<p><strong>Abstract</strong>: The establishment of exotic invasive species, including plants, has been linked to the decline of some amphibian populations.<br />Of particular concern with invasive plants, from an amphibian conservation perspective, is that they are disproportionately<br />wetland or riparian species. Recent evidence suggests that Chinese tallow (<em>Triadica sebifera</em>), an exotic deciduous tree species,<br />is expanding its range and becoming more abundant where it occurs in the United States. This is particularly relevant to<br />amphibian conservation considering that Chinese tallow tends to invade wetlands, and recent studies have demonstrated that<br />the leaf litter causes mortality of anuran eggs and larvae by reducing the dissolved oxygen and pH of water. The lethal effect<br />of Chinese tallow leaf litter is short lived and concentrated soon after leaf fall, typically December through to February in the<br />south-eastern United States. In this study, we were interested in determining the sub-lethal effects of Chinese tallow leaf litter<br />on the surfacing frequency and air-gulping behaviour of overwintering anuran larvae. <em>Lithobates catesbeianus</em> and <em>L. clamitans</em><br />clamitans are two frog species that commonly overwinter as aquatic larvae and extensively overlap in range with invasive<br />Chinese tallow, which may expose their tadpoles to the deleterious effects of the leaf litter. We conducted experiments where<br />we exposed tadpoles to four different concentrations of tallow leaf litter and recorded water chemistry and tadpole surfacing<br />frequency. We found that as Chinese tallow concentration increased, oxygen levels decreased. Both anuran species responded<br />similarly to our treatments and dissolved oxygen levels, where tadpoles swam to the water’s surface to air gulp at a significantly<br />higher rate in the treatments with greater tallow concentration. Such changes in behaviour induced by Chinese tallow could<br />have negative consequences on tadpole foraging efficiency and predator avoidance, ultimately reducing fitness. As biological<br />invasions will continue to be an important part of global change, more attention should be given to sub-lethal impacts, as they<br />pertain to fitness.</p>
<p><strong>Keywords</strong>: Anuran larvae; air gulping; Chinese tallow; leaf litter; invasive plants</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1051-03-effects-of-chinese-tallow-leaf-litter-on-water-chemistry-and-surfacing-behaviour-of-anuran-larvae?format=html</guid>
           <description><![CDATA[<p>pp. 326-332</p>
<p><strong>Authors</strong>: Daniel Saenz &amp; Cory K. Adams</p>
<p><strong>Abstract</strong>: The establishment of exotic invasive species, including plants, has been linked to the decline of some amphibian populations.<br />Of particular concern with invasive plants, from an amphibian conservation perspective, is that they are disproportionately<br />wetland or riparian species. Recent evidence suggests that Chinese tallow (<em>Triadica sebifera</em>), an exotic deciduous tree species,<br />is expanding its range and becoming more abundant where it occurs in the United States. This is particularly relevant to<br />amphibian conservation considering that Chinese tallow tends to invade wetlands, and recent studies have demonstrated that<br />the leaf litter causes mortality of anuran eggs and larvae by reducing the dissolved oxygen and pH of water. The lethal effect<br />of Chinese tallow leaf litter is short lived and concentrated soon after leaf fall, typically December through to February in the<br />south-eastern United States. In this study, we were interested in determining the sub-lethal effects of Chinese tallow leaf litter<br />on the surfacing frequency and air-gulping behaviour of overwintering anuran larvae. <em>Lithobates catesbeianus</em> and <em>L. clamitans</em><br />clamitans are two frog species that commonly overwinter as aquatic larvae and extensively overlap in range with invasive<br />Chinese tallow, which may expose their tadpoles to the deleterious effects of the leaf litter. We conducted experiments where<br />we exposed tadpoles to four different concentrations of tallow leaf litter and recorded water chemistry and tadpole surfacing<br />frequency. We found that as Chinese tallow concentration increased, oxygen levels decreased. Both anuran species responded<br />similarly to our treatments and dissolved oxygen levels, where tadpoles swam to the water’s surface to air gulp at a significantly<br />higher rate in the treatments with greater tallow concentration. Such changes in behaviour induced by Chinese tallow could<br />have negative consequences on tadpole foraging efficiency and predator avoidance, ultimately reducing fitness. As biological<br />invasions will continue to be an important part of global change, more attention should be given to sub-lethal impacts, as they<br />pertain to fitness.</p>
<p><strong>Keywords</strong>: Anuran larvae; air gulping; Chinese tallow; leaf litter; invasive plants</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:37:57 +0100</pubDate>
       </item>
              <item>
           <title>02. Amphibian species assemblages in a tropical forest of Bangladesh</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1050-02-amphibian-species-assemblages-in-a-tropical-forest-of-bangladesh?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1050-02-amphibian-species-assemblages-in-a-tropical-forest-of-bangladesh/file" length="1780098" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1050-02-amphibian-species-assemblages-in-a-tropical-forest-of-bangladesh/file"
                fileSize="1780098"
                type="application/pdf"
                medium="document"
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           <media:title type="plain">02. Amphibian species assemblages in a tropical forest of Bangladesh</media:title>
           <media:description type="html"><![CDATA[<p>pp. 318-325</p>
<p><strong>Authors</strong>: Animesh Ghose, Jiban Chandra Deb, Kwaku Brako Dakwa, Jay Prakash Ray &amp; AHM Ali<br />Reza5</p>
<p><strong>Abstract</strong>: Tropical forests are considered one of the most important biogeographic zones for amphibian species diversity. As a tropical<br />country in Asia, Bangladesh implements different types of forest management practices in its forests, which might affect<br />prevailing forest quality in the existing forest types. The current state of information on the impact of habitat alteration<br />on amphibian species assemblages in Bangladesh is inadequate. To evaluate this, we conducted a study in Khadimnagar<br />National Park (KNP) in north-eastern Bangladesh. We used a combination of several common amphibian study techniques<br />in 15 pre-marked transects covering three major habitat types in KNP: forest edge, forest interior and swamp area. Twelve<br />anuran species belonging to eleven genera and six families were recorded during the study period. <em>Euphlyctis cyanophlyctis</em><br />was the most abundant species, representing 51.7% of the recorded individuals, followed by <em>Fejervarya</em> spp. (18.9%); the<br />remaining 10 species altogether recorded less than 30% of the total abundance. <em>Duttaphrynus melanostictus</em>,<em> Kaloula pulchra</em><br />and <em>Raorchestes parvulus</em> in particular occurred with very low abundance. Species richness, Shannon-Wiener diversity index,<br />and evenness index value indicated that the amphibian species assemblage in the forest interior is more diverse than the forest<br />edge and swamp area.</p>
<p><strong>Keywords</strong>: Amphibian, species assemblages, abundance, diversity, habitat types, tropical forest</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1050-02-amphibian-species-assemblages-in-a-tropical-forest-of-bangladesh?format=html</guid>
           <description><![CDATA[<p>pp. 318-325</p>
<p><strong>Authors</strong>: Animesh Ghose, Jiban Chandra Deb, Kwaku Brako Dakwa, Jay Prakash Ray &amp; AHM Ali<br />Reza5</p>
<p><strong>Abstract</strong>: Tropical forests are considered one of the most important biogeographic zones for amphibian species diversity. As a tropical<br />country in Asia, Bangladesh implements different types of forest management practices in its forests, which might affect<br />prevailing forest quality in the existing forest types. The current state of information on the impact of habitat alteration<br />on amphibian species assemblages in Bangladesh is inadequate. To evaluate this, we conducted a study in Khadimnagar<br />National Park (KNP) in north-eastern Bangladesh. We used a combination of several common amphibian study techniques<br />in 15 pre-marked transects covering three major habitat types in KNP: forest edge, forest interior and swamp area. Twelve<br />anuran species belonging to eleven genera and six families were recorded during the study period. <em>Euphlyctis cyanophlyctis</em><br />was the most abundant species, representing 51.7% of the recorded individuals, followed by <em>Fejervarya</em> spp. (18.9%); the<br />remaining 10 species altogether recorded less than 30% of the total abundance. <em>Duttaphrynus melanostictus</em>,<em> Kaloula pulchra</em><br />and <em>Raorchestes parvulus</em> in particular occurred with very low abundance. Species richness, Shannon-Wiener diversity index,<br />and evenness index value indicated that the amphibian species assemblage in the forest interior is more diverse than the forest<br />edge and swamp area.</p>
<p><strong>Keywords</strong>: Amphibian, species assemblages, abundance, diversity, habitat types, tropical forest</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:37:56 +0100</pubDate>
       </item>
              <item>
           <title>01. Toxicity impact of butachlor on the development of green toad [i]Bufotes viridis[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1049-01-toxicity-impact-of-butachlor-on-the-development-of-green-toad-i-bufotes-viridis-i?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1049-01-toxicity-impact-of-butachlor-on-the-development-of-green-toad-i-bufotes-viridis-i/file" length="1948031" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1049-01-toxicity-impact-of-butachlor-on-the-development-of-green-toad-i-bufotes-viridis-i/file"
                fileSize="1948031"
                type="application/pdf"
                medium="document"
           />
           <media:title type="plain">01. Toxicity impact of butachlor on the development of green toad [i]Bufotes viridis[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp. 307-317</p>
<p><strong>Authors</strong>: Zahra Mossadeghi, Zeinab Parvaresh, Nazihe Seddighi, Fatemeh Roushenas, Samira Rahimi,<br />Elmira Hasani, Zahra Derakhshan &amp; Mohsen Nokhbatolfoghahai</p>
<p><strong>Abstract</strong>: Butachlor is the most commonly used herbicide on rice paddy fields in Asian countries. Paddy fields are habitats commonly<br />used for reproduction by many species of amphibians. We examined the effects of butachlor on <em>Bufotes viridis</em> development.<br />Amplectant pairs of <em>B. viridis</em> were kept in the laboratory in an aquarium overnight, and their spawn collected the next morning.<br />Eggs were exposed to butachlor at different concentrations (0.1, 0.2, 0.8, 1, 2, 3.5, 7, 14μg/l), all lower than the concentration<br />used in the area (rice paddy fields) by farmers. Eggs were allowed to develop to Gosner stage 24 and their developmental<br />patterns compared with those reared in normal conditions (control). In order to examine whether jelly coats have a significant<br />role in the protection of developing eggs from the toxin, another group of eggs were de-jellied and treated in the same<br />procedure. The LC50 value of butachlor was calculated as 14μg/l and 7μg/l after 96h for jellied eggs and de-jellied eggs<br />respectively. Butachlor lead to a range of external and internal body malformations. Butachlor concentrations of 2μg/l, 7μg/l<br />and 14μg/l reduced embryonic growth and development. A high mortality rate and both internal and external abnormalities<br />were observed at lower concentrations than used in fields, suggesting that butachlor can have significant negative effects on<br />amphibians where this herbicide is used.</p>
<p><strong>Keywords</strong>: amphibian; <em>Bufotes viridis</em>; butachlor; embryo; embryonic development; de-jellied egg</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-27-number-4-october-2017/1049-01-toxicity-impact-of-butachlor-on-the-development-of-green-toad-i-bufotes-viridis-i?format=html</guid>
           <description><![CDATA[<p>pp. 307-317</p>
<p><strong>Authors</strong>: Zahra Mossadeghi, Zeinab Parvaresh, Nazihe Seddighi, Fatemeh Roushenas, Samira Rahimi,<br />Elmira Hasani, Zahra Derakhshan &amp; Mohsen Nokhbatolfoghahai</p>
<p><strong>Abstract</strong>: Butachlor is the most commonly used herbicide on rice paddy fields in Asian countries. Paddy fields are habitats commonly<br />used for reproduction by many species of amphibians. We examined the effects of butachlor on <em>Bufotes viridis</em> development.<br />Amplectant pairs of <em>B. viridis</em> were kept in the laboratory in an aquarium overnight, and their spawn collected the next morning.<br />Eggs were exposed to butachlor at different concentrations (0.1, 0.2, 0.8, 1, 2, 3.5, 7, 14μg/l), all lower than the concentration<br />used in the area (rice paddy fields) by farmers. Eggs were allowed to develop to Gosner stage 24 and their developmental<br />patterns compared with those reared in normal conditions (control). In order to examine whether jelly coats have a significant<br />role in the protection of developing eggs from the toxin, another group of eggs were de-jellied and treated in the same<br />procedure. The LC50 value of butachlor was calculated as 14μg/l and 7μg/l after 96h for jellied eggs and de-jellied eggs<br />respectively. Butachlor lead to a range of external and internal body malformations. Butachlor concentrations of 2μg/l, 7μg/l<br />and 14μg/l reduced embryonic growth and development. A high mortality rate and both internal and external abnormalities<br />were observed at lower concentrations than used in fields, suggesting that butachlor can have significant negative effects on<br />amphibians where this herbicide is used.</p>
<p><strong>Keywords</strong>: amphibian; <em>Bufotes viridis</em>; butachlor; embryo; embryonic development; de-jellied egg</p>]]></description>
           <author>info@sarahberryonline.com (Sarah Berry)</author>
           <category>Volume 27, Number 4, October 2017</category>
           <pubDate>Sun, 01 Oct 2017 15:37:55 +0100</pubDate>
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