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       <title>Volume 8, Number 2, April 1998 - British Herpetological Society</title>
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       <url>https://www.thebhs.org/joomlatools-files/docman-images/HJ08-2__Front-Cover.jpg</url>
           <title>Volume 8, Number 2, April 1998 - British Herpetological Society</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998?format=html</link>
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           <title>08. Anuran assemblages in Crasto forest ponds (Sergipe State, Brazil) comparative structure and calling activity patterns</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1533-08-anuran-assemblages-in-crasto-forest-ponds-sergipe-state-brazil-comparative-structure-and-calling-activity-patterns?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1533-08-anuran-assemblages-in-crasto-forest-ponds-sergipe-state-brazil-comparative-structure-and-calling-activity-patterns/file" length="489458" type="application/pdf" />
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                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1533-08-anuran-assemblages-in-crasto-forest-ponds-sergipe-state-brazil-comparative-structure-and-calling-activity-patterns/file"
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           <media:title type="plain">08. Anuran assemblages in Crasto forest ponds (Sergipe State, Brazil) comparative structure and calling activity patterns</media:title>
           <media:description type="html"><![CDATA[<p>pp.11-113</p>
<p><strong>Authors</strong>:&nbsp;Cristina Arzabe, Cynara Xavier De Carvalho And Marcos A. Goes Costa</p>]]></media:description>
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           <description><![CDATA[<p>pp.11-113</p>
<p><strong>Authors</strong>:&nbsp;Cristina Arzabe, Cynara Xavier De Carvalho And Marcos A. Goes Costa</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:56 +0000</pubDate>
       </item>
              <item>
           <title>07. Natural history of [i]Tropidurus spinulosus[/i] (Squamata: Tropiduridae) from the dry chaco of Salta, Argentina</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1532-07-natural-history-of-tropidurus-spinulosus-squamata-tropiduridae-from-the-dry-chaco-of-salta-argentina?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1532-07-natural-history-of-tropidurus-spinulosus-squamata-tropiduridae-from-the-dry-chaco-of-salta-argentina/file" length="550138" type="application/pdf" />
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                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1532-07-natural-history-of-tropidurus-spinulosus-squamata-tropiduridae-from-the-dry-chaco-of-salta-argentina/file"
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           <media:title type="plain">07. Natural history of [i]Tropidurus spinulosus[/i] (Squamata: Tropiduridae) from the dry chaco of Salta, Argentina</media:title>
           <media:description type="html"><![CDATA[<p>pp.107-110</p>
<p><strong>Authors</strong>:&nbsp;Félix B. Cruz</p>]]></media:description>
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           <description><![CDATA[<p>pp.107-110</p>
<p><strong>Authors</strong>:&nbsp;Félix B. Cruz</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:55 +0000</pubDate>
       </item>
              <item>
           <title>06. Reproduction of the viviparous lizard [i]Liolaemus elongatus[/i] in the highlands of southern South America plastic cycles in response to climate</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1531-06-reproduction-of-the-viviparous-lizard-liolaemus-elongatus-in-the-highlands-of-southern-south-america-plastic-cycles-in-response-to-climate?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1531-06-reproduction-of-the-viviparous-lizard-liolaemus-elongatus-in-the-highlands-of-southern-south-america-plastic-cycles-in-response-to-climate/file" length="751638" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1531-06-reproduction-of-the-viviparous-lizard-liolaemus-elongatus-in-the-highlands-of-southern-south-america-plastic-cycles-in-response-to-climate/file"
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           <media:title type="plain">06. Reproduction of the viviparous lizard [i]Liolaemus elongatus[/i] in the highlands of southern South America plastic cycles in response to climate</media:title>
           <media:description type="html"><![CDATA[<p>pp.99-105</p>
<p><strong>Authors</strong>:&nbsp;Nora R. Ibargüengoytía And Victor E. Cussac</p>
<p><strong>Abstract</strong>:&nbsp;Squamate viviparity has evolved on several occasions, and probably independently within the genus <em>Liolaemus</em> itself. Hypotheses about the origin of reptilian viviparity emphasize the advantage of providing an adequate thermal environment for the embryo. At the same time, high latitudes and altitudes limit the availability of heat to perform vitellogenesis and gestation. The genus <em>Liolaemus</em> includes both oviparous and viviparous modes of reproduction, as well as reproductive cycles with great variations in the timing of the events. In the present work maximum juvenile size, sexual dimorphism, gonadal cycle and litter size of viviparous <em>Liolaemus elongatus</em> were studied. Female lizards may have annual or biennial cycles, but males reproduce annually in synchronization with the female cycle. Phenotypic plasticity may be one way that allows the species to cope with environmental constraints, and may be a reproductive adaptation that <em>Liolaemus</em> has evolved in response to the the cold climate in the highlands of southern South America.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1531-06-reproduction-of-the-viviparous-lizard-liolaemus-elongatus-in-the-highlands-of-southern-south-america-plastic-cycles-in-response-to-climate?format=html</guid>
           <description><![CDATA[<p>pp.99-105</p>
<p><strong>Authors</strong>:&nbsp;Nora R. Ibargüengoytía And Victor E. Cussac</p>
<p><strong>Abstract</strong>:&nbsp;Squamate viviparity has evolved on several occasions, and probably independently within the genus <em>Liolaemus</em> itself. Hypotheses about the origin of reptilian viviparity emphasize the advantage of providing an adequate thermal environment for the embryo. At the same time, high latitudes and altitudes limit the availability of heat to perform vitellogenesis and gestation. The genus <em>Liolaemus</em> includes both oviparous and viviparous modes of reproduction, as well as reproductive cycles with great variations in the timing of the events. In the present work maximum juvenile size, sexual dimorphism, gonadal cycle and litter size of viviparous <em>Liolaemus elongatus</em> were studied. Female lizards may have annual or biennial cycles, but males reproduce annually in synchronization with the female cycle. Phenotypic plasticity may be one way that allows the species to cope with environmental constraints, and may be a reproductive adaptation that <em>Liolaemus</em> has evolved in response to the the cold climate in the highlands of southern South America.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:54 +0000</pubDate>
       </item>
              <item>
           <title>05. Reproductive dynamics of a population of small marbled newts ([i]Triturus marmoratus pygmaeus[/i]) in south western Spain</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1530-05-reproductive-dynamics-of-a-population-of-small-marbled-newts-triturus-marmoratus-pygmaeus-in-south-western-spain?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1530-05-reproductive-dynamics-of-a-population-of-small-marbled-newts-triturus-marmoratus-pygmaeus-in-south-western-spain/file" length="1424280" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1530-05-reproductive-dynamics-of-a-population-of-small-marbled-newts-triturus-marmoratus-pygmaeus-in-south-western-spain/file"
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           <media:title type="plain">05. Reproductive dynamics of a population of small marbled newts ([i]Triturus marmoratus pygmaeus[/i]) in south western Spain</media:title>
           <media:description type="html"><![CDATA[<p>pp.93-98</p>
<p><strong>Authors</strong>:&nbsp;Carmen Díaz- Paniagua</p>
<p><strong>Abstract</strong>:&nbsp;A breeding population of small marbled newts in a temporary pond in SW Spain was sampled over five successive years. Males and females entered the pond just after it flooded in autumn. The adult aquatic season persisted until March or April, with maximum capture rates occurring mostly in January. Several sampling methods were used of which the most efficient was funnel trapping. Recapture rates were low. The population was estimated at about 1000 newts in 1987. Sex ratio did not differ from 1:1 in three seasons. In the other two seasons, which were characterized by low autumn rainfall, males outnumbered females by 2:1, probably as a result of many females failing to enter the pond to breed in those years. In the last two study years, the mean body size of newts was smaller than in previous years, possibly as a consequence of the adverse conditions of the two preceding autumns, which would have had repercussions for the growth of juveniles. An increase in physical condition and individual body mass throughout the aquatic season was observed in both sexes, confirming that the adult aquatic phase is advantageous for growth and maintenance of newts, as well as being necessary for reproduction. The age structure of the population was obtained in one of the seasons. Most males and females were 2-3 years old and a small percentage was one year old. The frequency of 1 year old mature females was lower than that of males. Females showed higher survival rates than males.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1530-05-reproductive-dynamics-of-a-population-of-small-marbled-newts-triturus-marmoratus-pygmaeus-in-south-western-spain?format=html</guid>
           <description><![CDATA[<p>pp.93-98</p>
<p><strong>Authors</strong>:&nbsp;Carmen Díaz- Paniagua</p>
<p><strong>Abstract</strong>:&nbsp;A breeding population of small marbled newts in a temporary pond in SW Spain was sampled over five successive years. Males and females entered the pond just after it flooded in autumn. The adult aquatic season persisted until March or April, with maximum capture rates occurring mostly in January. Several sampling methods were used of which the most efficient was funnel trapping. Recapture rates were low. The population was estimated at about 1000 newts in 1987. Sex ratio did not differ from 1:1 in three seasons. In the other two seasons, which were characterized by low autumn rainfall, males outnumbered females by 2:1, probably as a result of many females failing to enter the pond to breed in those years. In the last two study years, the mean body size of newts was smaller than in previous years, possibly as a consequence of the adverse conditions of the two preceding autumns, which would have had repercussions for the growth of juveniles. An increase in physical condition and individual body mass throughout the aquatic season was observed in both sexes, confirming that the adult aquatic phase is advantageous for growth and maintenance of newts, as well as being necessary for reproduction. The age structure of the population was obtained in one of the seasons. Most males and females were 2-3 years old and a small percentage was one year old. The frequency of 1 year old mature females was lower than that of males. Females showed higher survival rates than males.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:53 +0000</pubDate>
       </item>
              <item>
           <title>03. Body temperatures of captive tortoises at high altitude in Zimbabwe, with comments on the use of living models</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1528-03-body-temperatures-of-captive-tortoises-at-high-altitude-in-zimbabwe-with-comments-on-the-use-of-living-models?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1528-03-body-temperatures-of-captive-tortoises-at-high-altitude-in-zimbabwe-with-comments-on-the-use-of-living-models/file" length="699213" type="application/pdf" />
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                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1528-03-body-temperatures-of-captive-tortoises-at-high-altitude-in-zimbabwe-with-comments-on-the-use-of-living-models/file"
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           <media:title type="plain">03. Body temperatures of captive tortoises at high altitude in Zimbabwe, with comments on the use of living models</media:title>
           <media:description type="html"><![CDATA[<p>pp.79-84</p>
<p><strong>Authors</strong>:&nbsp;Adrian Hailey And John P. Loveridge</p>
<p><strong>Abstract</strong>:&nbsp;It is difficult to devise physical models which precisely mimic the body temperatures (T<sub>b</sub> 's) of large reptiles in the field. Studies of large reptiles have the compensating advantage that individuals can be fol lowed for long periods, so that translocated individuals can be used as ' living models'. We compare T<sub>b</sub>'s of two tortoise species in an enclosure in Harare (altitude 1500 m) with those in the field at Sengwa (900m), where mean air temperatures were about 5°C higher. Kinixys spekii, which occurs naturally near Harare, had similar T<sub>b</sub> 's at the two sites (means 27.6 and 27.0°C, respectively). Geochelone pardalis had significantly lower T<sub>b</sub> 's in Harare (29. 1 °C) than at Sengwa (32.6°C), even though activity was shifted towards midday in Harare. The inability to reach high T<sub>b</sub> during activity may explain the absence of G. pardalis near Harare, and the distribution of this species in southern Africa.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1528-03-body-temperatures-of-captive-tortoises-at-high-altitude-in-zimbabwe-with-comments-on-the-use-of-living-models?format=html</guid>
           <description><![CDATA[<p>pp.79-84</p>
<p><strong>Authors</strong>:&nbsp;Adrian Hailey And John P. Loveridge</p>
<p><strong>Abstract</strong>:&nbsp;It is difficult to devise physical models which precisely mimic the body temperatures (T<sub>b</sub> 's) of large reptiles in the field. Studies of large reptiles have the compensating advantage that individuals can be fol lowed for long periods, so that translocated individuals can be used as ' living models'. We compare T<sub>b</sub>'s of two tortoise species in an enclosure in Harare (altitude 1500 m) with those in the field at Sengwa (900m), where mean air temperatures were about 5°C higher. Kinixys spekii, which occurs naturally near Harare, had similar T<sub>b</sub> 's at the two sites (means 27.6 and 27.0°C, respectively). Geochelone pardalis had significantly lower T<sub>b</sub> 's in Harare (29. 1 °C) than at Sengwa (32.6°C), even though activity was shifted towards midday in Harare. The inability to reach high T<sub>b</sub> during activity may explain the absence of G. pardalis near Harare, and the distribution of this species in southern Africa.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:52 +0000</pubDate>
       </item>
              <item>
           <title>04. Morphological variation in the lacertid [i]Gallotia simonyi machadoi[/i] and a comparison with the extinct [i]Gallotia simonyi simonyi[/i] from El Hierro (Canary Is )</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1529-04-morphological-variation-in-the-lacertid-gallotia-simonyi-machadoi-and-a-comparison-with-the-extinct-gallotia-simonyi-simonyi-from-el-hierro-canary-is?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1529-04-morphological-variation-in-the-lacertid-gallotia-simonyi-machadoi-and-a-comparison-with-the-extinct-gallotia-simonyi-simonyi-from-el-hierro-canary-is/file" length="762631" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1529-04-morphological-variation-in-the-lacertid-gallotia-simonyi-machadoi-and-a-comparison-with-the-extinct-gallotia-simonyi-simonyi-from-el-hierro-canary-is/file"
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           <media:title type="plain">04. Morphological variation in the lacertid [i]Gallotia simonyi machadoi[/i] and a comparison with the extinct [i]Gallotia simonyi simonyi[/i] from El Hierro (Canary Is )</media:title>
           <media:description type="html"><![CDATA[<p>pp.85-91</p>
<p><strong>Authors</strong>:&nbsp;M. A. Rodríguez-domínguez , C. Castillo , J. J. Coello And M. Molina-borja</p>
<p><strong>Abstract</strong>:&nbsp;Morphological variation was investigated in 56 live adult specimens (3 1 male, 25 female) and ten dead near-hatching embryos of <em>G. simonyi machadoi</em> from the "Centro de Reproducción e Investigación del lagarto gigante del Hierro" (Frontera, El Hierro). Dimensions, scalation and teeth traits were measured and quantified. Males and females differed significantly (multivariate analysis of variance) in most of these traits, with values for males being greater than those for females. All traits significantly increased with SVL at a greater rate in males than in females, except for body weight, where no significant difference was found. A qualitative comparison between data from <em>G. s. machadoi</em> and those for ten <em>G. s. simonyi</em> showed that for most biometric traits, ranges overlapped for the two subspecies, but mean and maximum values were higher in <em>G. s. simonyi</em>. Hind limb length increased at a greater rate relative to SVL in<em> G. s. simonyi</em> than in <em>G. s. machadoi.</em></p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1529-04-morphological-variation-in-the-lacertid-gallotia-simonyi-machadoi-and-a-comparison-with-the-extinct-gallotia-simonyi-simonyi-from-el-hierro-canary-is?format=html</guid>
           <description><![CDATA[<p>pp.85-91</p>
<p><strong>Authors</strong>:&nbsp;M. A. Rodríguez-domínguez , C. Castillo , J. J. Coello And M. Molina-borja</p>
<p><strong>Abstract</strong>:&nbsp;Morphological variation was investigated in 56 live adult specimens (3 1 male, 25 female) and ten dead near-hatching embryos of <em>G. simonyi machadoi</em> from the "Centro de Reproducción e Investigación del lagarto gigante del Hierro" (Frontera, El Hierro). Dimensions, scalation and teeth traits were measured and quantified. Males and females differed significantly (multivariate analysis of variance) in most of these traits, with values for males being greater than those for females. All traits significantly increased with SVL at a greater rate in males than in females, except for body weight, where no significant difference was found. A qualitative comparison between data from <em>G. s. machadoi</em> and those for ten <em>G. s. simonyi</em> showed that for most biometric traits, ranges overlapped for the two subspecies, but mean and maximum values were higher in <em>G. s. simonyi</em>. Hind limb length increased at a greater rate relative to SVL in<em> G. s. simonyi</em> than in <em>G. s. machadoi.</em></p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:52 +0000</pubDate>
       </item>
              <item>
           <title>02. Growth, allometry and sexual dimorphism in the Florida box turtle, [i]Terrapene carolina bauri[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1527-02-growth-allometry-and-sexual-dimorphism-in-the-florida-box-turtle-terrapene-carolina-bauri?format=html</link>
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           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1527-02-growth-allometry-and-sexual-dimorphism-in-the-florida-box-turtle-terrapene-carolina-bauri/file"
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           <media:title type="plain">02. Growth, allometry and sexual dimorphism in the Florida box turtle, [i]Terrapene carolina bauri[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp.72-78</p>
<p><strong>Authors</strong>:&nbsp;Carl H. Ernst , James C . Wilgenbusch , Timothy P. Boucher And Steven W. Sekscienski</p>
<p><strong>Abstract</strong>:&nbsp;Male Florida box turtles, <em>Terrapene carolina bauri</em>, grow proportionally longer relative to their height and width, than do females, resulting in a longer, flatter carapace, whereas females develop shorter, higher, and slightly narrower carapaces, possibly as an adaptation to accommodate hard-shelled eggs before oviposition. The subspecies has a typical growth pattern for a North American emydine turtle. Growth is rapid in juveniles, but starts to slow once maturity is reached at an age of 12-13 years. Growth rates approach an asymptote at about age 17 years in males and 16 years in females; very little growth occurs after age 20 years. Florida <em>T. c. bauri</em> grows at a slower annual rate than does <em>T. c. carolina</em> from Maryland despite having a longer annual activity and growth period. The data presented here may be considered to represent the average growth pattern for <em>T. c. bauri</em> in Florida. The cervical scute and all vertebral scutes have a greater width:length ratio in juveniles, but this ratio declines as the scutes lengthen with elongation of the carapace; however, the rate of increase in length varies among the scutes</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1527-02-growth-allometry-and-sexual-dimorphism-in-the-florida-box-turtle-terrapene-carolina-bauri?format=html</guid>
           <description><![CDATA[<p>pp.72-78</p>
<p><strong>Authors</strong>:&nbsp;Carl H. Ernst , James C . Wilgenbusch , Timothy P. Boucher And Steven W. Sekscienski</p>
<p><strong>Abstract</strong>:&nbsp;Male Florida box turtles, <em>Terrapene carolina bauri</em>, grow proportionally longer relative to their height and width, than do females, resulting in a longer, flatter carapace, whereas females develop shorter, higher, and slightly narrower carapaces, possibly as an adaptation to accommodate hard-shelled eggs before oviposition. The subspecies has a typical growth pattern for a North American emydine turtle. Growth is rapid in juveniles, but starts to slow once maturity is reached at an age of 12-13 years. Growth rates approach an asymptote at about age 17 years in males and 16 years in females; very little growth occurs after age 20 years. Florida <em>T. c. bauri</em> grows at a slower annual rate than does <em>T. c. carolina</em> from Maryland despite having a longer annual activity and growth period. The data presented here may be considered to represent the average growth pattern for <em>T. c. bauri</em> in Florida. The cervical scute and all vertebral scutes have a greater width:length ratio in juveniles, but this ratio declines as the scutes lengthen with elongation of the carapace; however, the rate of increase in length varies among the scutes</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:51 +0000</pubDate>
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           <title>01. Resorption of oviductal eggs and embryos in squamate reptiles</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1526-01-resorption-of-oviductal-eggs-and-embryos-in-squamate-reptiles?format=html</link>
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           <media:title type="plain">01. Resorption of oviductal eggs and embryos in squamate reptiles</media:title>
           <media:description type="html"><![CDATA[<p>pp.65-71&nbsp;</p>
<p><strong>Authors</strong>:&nbsp;Daniel G. Blackburn</p>
<p><strong>Abstract</strong>:&nbsp;Among squamate reptiles, gravid females are frequently said to be able to resorb infertile and malformed eggs from their oviducts. This pattern, if it existed, would allow females to recycle nutrients from abortive attempts at reproduction, and to increase lifetime reproductive potential by modul . ating reproductive effort according to environmental circumstances. However, a review of the literature reveals that evidence for oviductal egg resorption is weak, and does not preclude other fates for abortive eggs (egg retention or expulsion). Furthermore, for the oviduct to resorb eggs would require that it have the functional properties of the digestive tract, properties that may be incompatible with its several reproductive functions. Future work should not assume oviductal egg resorption in squamates without definitive evidence that the eggs are not simply aborted or retained by females foll owing absorption of water.</p>]]></media:description>
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           <description><![CDATA[<p>pp.65-71&nbsp;</p>
<p><strong>Authors</strong>:&nbsp;Daniel G. Blackburn</p>
<p><strong>Abstract</strong>:&nbsp;Among squamate reptiles, gravid females are frequently said to be able to resorb infertile and malformed eggs from their oviducts. This pattern, if it existed, would allow females to recycle nutrients from abortive attempts at reproduction, and to increase lifetime reproductive potential by modul . ating reproductive effort according to environmental circumstances. However, a review of the literature reveals that evidence for oviductal egg resorption is weak, and does not preclude other fates for abortive eggs (egg retention or expulsion). Furthermore, for the oviduct to resorb eggs would require that it have the functional properties of the digestive tract, properties that may be incompatible with its several reproductive functions. Future work should not assume oviductal egg resorption in squamates without definitive evidence that the eggs are not simply aborted or retained by females foll owing absorption of water.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:50 +0000</pubDate>
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           <title>Volume 8, Number 2, April 1998 - Full Issue</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1525-volume-8-number-2-april-1998-full-issue?format=html</link>
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           <media:title type="plain">Volume 8, Number 2, April 1998 - Full Issue</media:title>
           <media:description type="html"><![CDATA[]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1525-volume-8-number-2-april-1998-full-issue?format=html</guid>
           <description><![CDATA[]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:49 +0000</pubDate>
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           <title>Table of Contents</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1524-table-of-contents-34?format=html</link>
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           <media:title type="plain">Table of Contents</media:title>
           <media:description type="html"><![CDATA[]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1524-table-of-contents-34?format=html</guid>
           <description><![CDATA[]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:48 +0000</pubDate>
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           <title>Front Cover</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1523-front-cover-42?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1523-front-cover-42/file" length="776135" type="application/pdf" />
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           <media:title type="plain">Front Cover</media:title>
           <media:description type="html"><![CDATA[]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-8-number-2-april-1998/1523-front-cover-42?format=html</guid>
           <description><![CDATA[]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 8, Number 2, April 1998</category>
           <pubDate>Fri, 02 Mar 2018 09:57:47 +0000</pubDate>
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