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       <title>Volume 1, Number 12, June 1991 - British Herpetological Society</title>
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       <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991?format=html</link>
              <image>
       <url>https://www.thebhs.org/joomlatools-files/docman-images/HJ01-12__Front-Cover.jpg</url>
           <title>Volume 1, Number 12, June 1991 - British Herpetological Society</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991?format=html</link>
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           <title>07. Preliminary study on the breeding pattern of the Egyptian tortoise, [i]Testudo kleinmanni[/i], in Israel</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1256-07-preliminary-study-on-the-breeding-pattern-of-the-egyptian-tortoise-testudo-kleinmanni-in-israel?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1256-07-preliminary-study-on-the-breeding-pattern-of-the-egyptian-tortoise-testudo-kleinmanni-in-israel/file" length="884536" type="application/pdf" />
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                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1256-07-preliminary-study-on-the-breeding-pattern-of-the-egyptian-tortoise-testudo-kleinmanni-in-israel/file"
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           <media:title type="plain">07. Preliminary study on the breeding pattern of the Egyptian tortoise, [i]Testudo kleinmanni[/i], in Israel</media:title>
           <media:description type="html"><![CDATA[<p>pp.574-577</p>
<p><strong>Authors</strong>:&nbsp;Eli Geffen And Heinrich Mendelssohn</p>
<p><strong>Abstract</strong>:&nbsp;Egyptian tortoises were collected in the field and X-rayed at 2-4 week intervals during two breeding seasons. Females laid 2-3 clutches per year, each consisting of 1-3 large eggs. The internesting period was estimated to be 20-30 days. The nest was a shallow pit at a base of a bush. The breeding biology of Testudo kleinmanni is similar to that of other small highly specialised tortoises.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1256-07-preliminary-study-on-the-breeding-pattern-of-the-egyptian-tortoise-testudo-kleinmanni-in-israel?format=html</guid>
           <description><![CDATA[<p>pp.574-577</p>
<p><strong>Authors</strong>:&nbsp;Eli Geffen And Heinrich Mendelssohn</p>
<p><strong>Abstract</strong>:&nbsp;Egyptian tortoises were collected in the field and X-rayed at 2-4 week intervals during two breeding seasons. Females laid 2-3 clutches per year, each consisting of 1-3 large eggs. The internesting period was estimated to be 20-30 days. The nest was a shallow pit at a base of a bush. The breeding biology of Testudo kleinmanni is similar to that of other small highly specialised tortoises.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:43 +0000</pubDate>
       </item>
              <item>
           <title>08. Visual stimuli and spontaneous locomotor patterns of common lizards, [i]Lacerta vivipara[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1257-08-visual-stimuli-and-spontaneous-locomotor-patterns-of-common-lizards-lacerta-vivipara?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1257-08-visual-stimuli-and-spontaneous-locomotor-patterns-of-common-lizards-lacerta-vivipara/file" length="778580" type="application/pdf" />
           <media:content
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           <media:title type="plain">08. Visual stimuli and spontaneous locomotor patterns of common lizards, [i]Lacerta vivipara[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp.577-579</p>
<p><strong>Authors</strong>:&nbsp;G. Cowlishaw And R. A. Avery</p>
<p><strong>Abstract</strong>:&nbsp;The movement pattern of adult male <em>Lacerta vivipara</em> travelling spontaneously along a wooden-walled channel&nbsp;was similar to the previously measured pattern of animals moving across an open space, comprising an alternation&nbsp;of short (-1 s) bursts of locomotion with even shorter (-0.1 s) pauses. Changing the structure and appearance of&nbsp;the walls of the channel altered the locomotor pattern. Grass turf separated from the lizards by glass h ad the greatest&nbsp;effect, causing a decrease in mean burst speed and an increase in mean pause duration. This persisted for 25 trials,&nbsp;suggesting that the response to the visual stimulus presented by turf was investigatory and not merely due to its&nbsp;novelty, whereas the smaller effect seen when the walls were of white card waned with time and so may have been&nbsp;primarily a response to change.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1257-08-visual-stimuli-and-spontaneous-locomotor-patterns-of-common-lizards-lacerta-vivipara?format=html</guid>
           <description><![CDATA[<p>pp.577-579</p>
<p><strong>Authors</strong>:&nbsp;G. Cowlishaw And R. A. Avery</p>
<p><strong>Abstract</strong>:&nbsp;The movement pattern of adult male <em>Lacerta vivipara</em> travelling spontaneously along a wooden-walled channel&nbsp;was similar to the previously measured pattern of animals moving across an open space, comprising an alternation&nbsp;of short (-1 s) bursts of locomotion with even shorter (-0.1 s) pauses. Changing the structure and appearance of&nbsp;the walls of the channel altered the locomotor pattern. Grass turf separated from the lizards by glass h ad the greatest&nbsp;effect, causing a decrease in mean burst speed and an increase in mean pause duration. This persisted for 25 trials,&nbsp;suggesting that the response to the visual stimulus presented by turf was investigatory and not merely due to its&nbsp;novelty, whereas the smaller effect seen when the walls were of white card waned with time and so may have been&nbsp;primarily a response to change.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:43 +0000</pubDate>
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           <title>06. Amphibians of the Whitemoor Channel early Flandrian site near Bosley, East Cheshire; with remarks on the fossil distribution of [i]Bufo calamita[/i] in Brita</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1255-06-amphibians-of-the-whitemoor-channel-early-flandrian-site-near-bosley-east-cheshire-with-remarks-on-the-fossil-distribution-of-bufo-calamita-in-brita?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1255-06-amphibians-of-the-whitemoor-channel-early-flandrian-site-near-bosley-east-cheshire-with-remarks-on-the-fossil-distribution-of-bufo-calamita-in-brita/file" length="1214776" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1255-06-amphibians-of-the-whitemoor-channel-early-flandrian-site-near-bosley-east-cheshire-with-remarks-on-the-fossil-distribution-of-bufo-calamita-in-brita/file"
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           <media:title type="plain">06. Amphibians of the Whitemoor Channel early Flandrian site near Bosley, East Cheshire; with remarks on the fossil distribution of [i]Bufo calamita[/i] in Brita</media:title>
           <media:description type="html"><![CDATA[<p>pp.568-573</p>
<p><strong>Authors</strong>:&nbsp;J. Alan Holman And Anthony J. Stuart</p>
<p><strong>Abstract</strong>:&nbsp;A lacustrine <em>Chara</em> marl (ea. 10,000-8,800 radiocarbon years BP) at the Whitemoor Channel Site near Bosley,&nbsp;East Cheshire, yielded fossil amphibian remains, including palmate newt <em>Trirurus helvericus</em>, smooth newt <em>Triturus&nbsp;vulgaris</em>, natterjack toad <em>Bufo calamira</em>, common toad <em>Bufo bufo</em>, common frog <em>Rana temporaria</em> and material&nbsp;belonging to these genera which probably represent the same five species. All of these species are extant and occur&nbsp;naturally in Britain today, although for the past two hundred years the natterjack toad <em>Bufo calamira</em> has occurred&nbsp;only locally in Britain, being essentially restricted to coastal dunes and inland heaths. The well-dated Flandrian&nbsp;(early Holocene) finds from Whitemoor Channel are an important addition to previous, poorly stratified, records&nbsp;from Cow Cave, Chudleigh, Devon, and Ightham Fissures, Sevenoaks, Kent. Taken together, these records&nbsp;demonstrate early colonisation of England by <em>B. calamira</em> after the last Cold Stage and suggest a wider geographical&nbsp;occurrence of the natterjack than in Britain today.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1255-06-amphibians-of-the-whitemoor-channel-early-flandrian-site-near-bosley-east-cheshire-with-remarks-on-the-fossil-distribution-of-bufo-calamita-in-brita?format=html</guid>
           <description><![CDATA[<p>pp.568-573</p>
<p><strong>Authors</strong>:&nbsp;J. Alan Holman And Anthony J. Stuart</p>
<p><strong>Abstract</strong>:&nbsp;A lacustrine <em>Chara</em> marl (ea. 10,000-8,800 radiocarbon years BP) at the Whitemoor Channel Site near Bosley,&nbsp;East Cheshire, yielded fossil amphibian remains, including palmate newt <em>Trirurus helvericus</em>, smooth newt <em>Triturus&nbsp;vulgaris</em>, natterjack toad <em>Bufo calamira</em>, common toad <em>Bufo bufo</em>, common frog <em>Rana temporaria</em> and material&nbsp;belonging to these genera which probably represent the same five species. All of these species are extant and occur&nbsp;naturally in Britain today, although for the past two hundred years the natterjack toad <em>Bufo calamira</em> has occurred&nbsp;only locally in Britain, being essentially restricted to coastal dunes and inland heaths. The well-dated Flandrian&nbsp;(early Holocene) finds from Whitemoor Channel are an important addition to previous, poorly stratified, records&nbsp;from Cow Cave, Chudleigh, Devon, and Ightham Fissures, Sevenoaks, Kent. Taken together, these records&nbsp;demonstrate early colonisation of England by <em>B. calamira</em> after the last Cold Stage and suggest a wider geographical&nbsp;occurrence of the natterjack than in Britain today.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:42 +0000</pubDate>
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           <title>05. Differences in thermoregulation between [i]Testudo hermanni[/i] and [i]Testudo marginata[/i] and their ecological significance</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1254-05-differences-in-thermoregulation-between-testudo-hermanni-and-testudo-marginata-and-their-ecological-significance?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1254-05-differences-in-thermoregulation-between-testudo-hermanni-and-testudo-marginata-and-their-ecological-significance/file" length="1127095" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1254-05-differences-in-thermoregulation-between-testudo-hermanni-and-testudo-marginata-and-their-ecological-significance/file"
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           <media:title type="plain">05. Differences in thermoregulation between [i]Testudo hermanni[/i] and [i]Testudo marginata[/i] and their ecological significance</media:title>
           <media:description type="html"><![CDATA[<p>pp.559-567</p>
<p><strong>Authors</strong>:&nbsp;Ronald E. Willemsen</p>
<p><strong>Abstract</strong>:&nbsp;The activity patterns and body temperatures of <em>T. hermanni</em> and <em>T. marginata</em> were studied in the Peloponnese&nbsp;(southern Greece) during May, June, August and October 1984.<br /><em>T. hermanni:</em><br />In May the daily activity patterns of <em>T. hermanni</em> were uni modal , in June and August they were bi modal. In&nbsp;August during the afternoon the activity increased significantly. in October the activity was very low.&nbsp;In August basking decreased significantly and mating increased significantly.&nbsp;During these four months no significant differences in body temperatures were found. In May a maximum body&nbsp;temperature of 35°C was found; in feeding tortoises a maximum temperature of 34°C. After May no temperatures&nbsp;over 32°C were found.<br /><em>T. marginata:</em><br />In May and June the activity patterns of <em>T. marginata</em> were bimodal with the highest activity during the afternoon.&nbsp;In August an uni modal low activity pattern was found during the afternoon. In October the activity of <em>T. marginata&nbsp;</em>was uni modal and shifted towards the middle of the day. Sexual activity was seen in October only.&nbsp;Body temperatures in all<em> T. marginata</em> samples were significantly higher than those in <em>T. hermanni</em>. During May a&nbsp;maximum body temperature of 36°C was found in basking tortoises, a maximum of 37°C in feeding tortoises.&nbsp;The trend towards lower body temperatures in summer was greater in <em>T. marginata</em> than in <em>T. hermanni</em>. Body&nbsp;temperatures found in feeding tortoises in October equalled those found in May.<br /><em>Ecological Consequences:</em><br />In southern Greece the habitat separation between <em>T. hermanni</em> and<em> T. marginata</em> can be explained by&nbsp;morphological differences and a higher body temperature tolerance in T. marginata. Differences in the annual cycle&nbsp;of activities might also be of importance as regards the habitat separation between both species.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1254-05-differences-in-thermoregulation-between-testudo-hermanni-and-testudo-marginata-and-their-ecological-significance?format=html</guid>
           <description><![CDATA[<p>pp.559-567</p>
<p><strong>Authors</strong>:&nbsp;Ronald E. Willemsen</p>
<p><strong>Abstract</strong>:&nbsp;The activity patterns and body temperatures of <em>T. hermanni</em> and <em>T. marginata</em> were studied in the Peloponnese&nbsp;(southern Greece) during May, June, August and October 1984.<br /><em>T. hermanni:</em><br />In May the daily activity patterns of <em>T. hermanni</em> were uni modal , in June and August they were bi modal. In&nbsp;August during the afternoon the activity increased significantly. in October the activity was very low.&nbsp;In August basking decreased significantly and mating increased significantly.&nbsp;During these four months no significant differences in body temperatures were found. In May a maximum body&nbsp;temperature of 35°C was found; in feeding tortoises a maximum temperature of 34°C. After May no temperatures&nbsp;over 32°C were found.<br /><em>T. marginata:</em><br />In May and June the activity patterns of <em>T. marginata</em> were bimodal with the highest activity during the afternoon.&nbsp;In August an uni modal low activity pattern was found during the afternoon. In October the activity of <em>T. marginata&nbsp;</em>was uni modal and shifted towards the middle of the day. Sexual activity was seen in October only.&nbsp;Body temperatures in all<em> T. marginata</em> samples were significantly higher than those in <em>T. hermanni</em>. During May a&nbsp;maximum body temperature of 36°C was found in basking tortoises, a maximum of 37°C in feeding tortoises.&nbsp;The trend towards lower body temperatures in summer was greater in <em>T. marginata</em> than in <em>T. hermanni</em>. Body&nbsp;temperatures found in feeding tortoises in October equalled those found in May.<br /><em>Ecological Consequences:</em><br />In southern Greece the habitat separation between <em>T. hermanni</em> and<em> T. marginata</em> can be explained by&nbsp;morphological differences and a higher body temperature tolerance in T. marginata. Differences in the annual cycle&nbsp;of activities might also be of importance as regards the habitat separation between both species.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:39 +0000</pubDate>
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              <item>
           <title>03. The distribution and breeding site characteristics of newts in Cumbria, England</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1252-03-the-distribution-and-breeding-site-characteristics-of-newts-in-cumbria-england?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1252-03-the-distribution-and-breeding-site-characteristics-of-newts-in-cumbria-england/file" length="1160850" type="application/pdf" />
           <media:content
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           <media:title type="plain">03. The distribution and breeding site characteristics of newts in Cumbria, England</media:title>
           <media:description type="html"><![CDATA[<p>pp.549-554</p>
<p><strong>Authors</strong>:&nbsp;J. S. Denton</p>
<p><strong>Abstract</strong>:&nbsp;The distribution and breeding site characteristics of the smooth newt, <em>Triturus vulgaris</em>, the palmate newt,&nbsp;<em>T. he!veticus</em> and the warty newt, <em>T. crisrarus</em> were investigated in Cumbria.<em> T. he!veticus</em> was the commonest species&nbsp;on the acidic rocks in the Lake District , but was not found in limestone areas.<em> T. crisrarus</em> was seldom found without&nbsp;the commoner<em> T. vulgaris</em>, and there was no evidence of the former preferring larger, deeper ponds than the latter.<br /><em>T. vulgaris</em> and<em> T. cristatus</em>, unlike <em>T. helvericus</em> were rarely found in water with pH&lt;6. T<em>. vulgaris</em> was usually&nbsp;found in water relatively rich in metal ions, while the reverse was true for <em>T. helveticus</em>.<br />Newts were found in ponds in a wide variety of terrestrial habitats, but most often in rough pasture land.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1252-03-the-distribution-and-breeding-site-characteristics-of-newts-in-cumbria-england?format=html</guid>
           <description><![CDATA[<p>pp.549-554</p>
<p><strong>Authors</strong>:&nbsp;J. S. Denton</p>
<p><strong>Abstract</strong>:&nbsp;The distribution and breeding site characteristics of the smooth newt, <em>Triturus vulgaris</em>, the palmate newt,&nbsp;<em>T. he!veticus</em> and the warty newt, <em>T. crisrarus</em> were investigated in Cumbria.<em> T. he!veticus</em> was the commonest species&nbsp;on the acidic rocks in the Lake District , but was not found in limestone areas.<em> T. crisrarus</em> was seldom found without&nbsp;the commoner<em> T. vulgaris</em>, and there was no evidence of the former preferring larger, deeper ponds than the latter.<br /><em>T. vulgaris</em> and<em> T. cristatus</em>, unlike <em>T. helvericus</em> were rarely found in water with pH&lt;6. T<em>. vulgaris</em> was usually&nbsp;found in water relatively rich in metal ions, while the reverse was true for <em>T. helveticus</em>.<br />Newts were found in ponds in a wide variety of terrestrial habitats, but most often in rough pasture land.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:38 +0000</pubDate>
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              <item>
           <title>04. Partitioning of water within the alligator ([i]Alligator mississippiensis[/i]) egg after 60 days of incubation</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1253-04-partitioning-of-water-within-the-alligator-alligator-mississippiensis-egg-after-60-days-of-incubation?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1253-04-partitioning-of-water-within-the-alligator-alligator-mississippiensis-egg-after-60-days-of-incubation/file" length="918754" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1253-04-partitioning-of-water-within-the-alligator-alligator-mississippiensis-egg-after-60-days-of-incubation/file"
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           <media:title type="plain">04. Partitioning of water within the alligator ([i]Alligator mississippiensis[/i]) egg after 60 days of incubation</media:title>
           <media:description type="html"><![CDATA[<p>pp.554-558</p>
<p><strong>Authors</strong>: D. C. Deeming And M. W. J. Ferguson</p>
<p><strong>Abstract</strong>:&nbsp;Eggs of <em>Alligator mississippiensis</em> were incubated up to day 60 of incubation under either dry conditions (on metal&nbsp;shelves, without a substrate) or wet conditions (on vermiculite). Incubation temperatures were 30°C and 33°C. Eggs&nbsp;on the shelves lost water during incubation; water loss from eggs on vermiculite was small, and in some cases,&nbsp;negligible. On day 60, after incubation at 30°C, eggs incubated on shelves had significantly less amniotic fluid and&nbsp;yolk sac than eggs incubated on vermiculite. In eggs incubated at 33°C, on day 60 amniotic fluid was absent and the&nbsp;mass of the yolk sac was smaller in eggs incubated under dry conditions. Embryo mass and the amount of allantoic&nbsp;fluid were unaffected by the extent of water loss from the eggs at both temperatures. The mass of allantoic fluid was&nbsp;correlated with the mass of the egg on day 60. Yolk sac mass at both temperatures was not correlated with egg mass&nbsp;on day 60 but was correlated with the water lost from the egg. These results suggest that (1) in alligator eggs, loss of&nbsp;water is borne primarily by the yolk sac; and (2) that retention of water in the allantois may be associated with a need&nbsp;to prevent a deleterious build-up of waste metabolites. This contrasts with the situation in avian eggs where water&nbsp;loss is borne primarily by the allantois and embryonic tissues.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1253-04-partitioning-of-water-within-the-alligator-alligator-mississippiensis-egg-after-60-days-of-incubation?format=html</guid>
           <description><![CDATA[<p>pp.554-558</p>
<p><strong>Authors</strong>: D. C. Deeming And M. W. J. Ferguson</p>
<p><strong>Abstract</strong>:&nbsp;Eggs of <em>Alligator mississippiensis</em> were incubated up to day 60 of incubation under either dry conditions (on metal&nbsp;shelves, without a substrate) or wet conditions (on vermiculite). Incubation temperatures were 30°C and 33°C. Eggs&nbsp;on the shelves lost water during incubation; water loss from eggs on vermiculite was small, and in some cases,&nbsp;negligible. On day 60, after incubation at 30°C, eggs incubated on shelves had significantly less amniotic fluid and&nbsp;yolk sac than eggs incubated on vermiculite. In eggs incubated at 33°C, on day 60 amniotic fluid was absent and the&nbsp;mass of the yolk sac was smaller in eggs incubated under dry conditions. Embryo mass and the amount of allantoic&nbsp;fluid were unaffected by the extent of water loss from the eggs at both temperatures. The mass of allantoic fluid was&nbsp;correlated with the mass of the egg on day 60. Yolk sac mass at both temperatures was not correlated with egg mass&nbsp;on day 60 but was correlated with the water lost from the egg. These results suggest that (1) in alligator eggs, loss of&nbsp;water is borne primarily by the yolk sac; and (2) that retention of water in the allantois may be associated with a need&nbsp;to prevent a deleterious build-up of waste metabolites. This contrasts with the situation in avian eggs where water&nbsp;loss is borne primarily by the allantois and embryonic tissues.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:38 +0000</pubDate>
       </item>
              <item>
           <title>02. Summer activity patterns and thermoregulation in the wall l izard, [i]Podarcis muralis[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1251-02-summer-activity-patterns-and-thermoregulation-in-the-wall-l-izard-podarcis-muralis?format=html</link>
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           <media:title type="plain">02. Summer activity patterns and thermoregulation in the wall l izard, [i]Podarcis muralis[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp.544-549</p>
<p><strong>Authors</strong>:&nbsp;Florentino Braña</p>
<p><strong>Abstract</strong>:&nbsp;Body temperature of active Podarcis muralis from Norefia (Asturias; Northern Spain) during summer averages&nbsp;33. 8°C (SO= 2.0, n = 116), and similar values were found in other close populations (grand mean: 33. 8°C, SO = 2.3,&nbsp;n = 171 ). There were no significant differences neither in body temperatures between populations nor between&nbsp;sex/age groups within populations. Daily activity pattern is bimodal, with depressed activity during the warmer&nbsp;hours at the midday. This pattern of activity, as well as the significant negative correlation between the percentage&nbsp;of lizards at sun and the environmental temperatures, are indicative of behavioural thermoregulation. The standard&nbsp;deviations of the mean body temperature and the slopes of the regressions of body temperature on environment&nbsp;temperatures are indicative of a relatively imprecise thermoregulation. Populations from the highest altitudes show&nbsp;a higher variability in body temperature and a greater dependence on the thermal environment.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1251-02-summer-activity-patterns-and-thermoregulation-in-the-wall-l-izard-podarcis-muralis?format=html</guid>
           <description><![CDATA[<p>pp.544-549</p>
<p><strong>Authors</strong>:&nbsp;Florentino Braña</p>
<p><strong>Abstract</strong>:&nbsp;Body temperature of active Podarcis muralis from Norefia (Asturias; Northern Spain) during summer averages&nbsp;33. 8°C (SO= 2.0, n = 116), and similar values were found in other close populations (grand mean: 33. 8°C, SO = 2.3,&nbsp;n = 171 ). There were no significant differences neither in body temperatures between populations nor between&nbsp;sex/age groups within populations. Daily activity pattern is bimodal, with depressed activity during the warmer&nbsp;hours at the midday. This pattern of activity, as well as the significant negative correlation between the percentage&nbsp;of lizards at sun and the environmental temperatures, are indicative of behavioural thermoregulation. The standard&nbsp;deviations of the mean body temperature and the slopes of the regressions of body temperature on environment&nbsp;temperatures are indicative of a relatively imprecise thermoregulation. Populations from the highest altitudes show&nbsp;a higher variability in body temperature and a greater dependence on the thermal environment.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:37 +0000</pubDate>
       </item>
              <item>
           <title>01. The Orientation behaviour of amphibians</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1250-01-the-orientation-behaviour-of-amphibians?format=html</link>
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           <media:title type="plain">01. The Orientation behaviour of amphibians</media:title>
           <media:description type="html"><![CDATA[<p>pp.541-544</p>
<p><strong>Authors</strong>: Ulrich Sinsch</p>]]></media:description>
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           <description><![CDATA[<p>pp.541-544</p>
<p><strong>Authors</strong>: Ulrich Sinsch</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:36 +0000</pubDate>
       </item>
              <item>
           <title>Volume 1, Number 12, June 1991 - Full Issue</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1249-volume-1-number-12-june-1991-full-issue?format=html</link>
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           <media:title type="plain">Volume 1, Number 12, June 1991 - Full Issue</media:title>
           <media:description type="html"><![CDATA[]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1249-volume-1-number-12-june-1991-full-issue?format=html</guid>
           <description><![CDATA[]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:35 +0000</pubDate>
       </item>
              <item>
           <title>Table of Contents</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1248-table-of-contents-8?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1248-table-of-contents-8/file" length="404881" type="application/pdf" />
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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-1-number-12-june-1991/1248-table-of-contents-8?format=html</guid>
           <description><![CDATA[]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:34 +0000</pubDate>
       </item>
              <item>
           <title>Front Cover</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1247-front-cover-16?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-1-number-12-june-1991/1247-front-cover-16/file" length="883701" 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-1-number-12-june-1991/1247-front-cover-16?format=html</guid>
           <description><![CDATA[]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 1, Number 12, June 1991</category>
           <pubDate>Thu, 01 Mar 2018 20:50:33 +0000</pubDate>
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