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       <title>Volume 7, Number 2, April 1997 - British Herpetological Society</title>
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       <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997?format=html</link>
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       <url>https://www.thebhs.org/joomlatools-files/docman-images/HJ07-2__Front-Cover.jpg</url>
           <title>Volume 7, Number 2, April 1997 - British Herpetological Society</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997?format=html</link>
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              <item>
           <title>09. Actual and osteochronological estimated age of natterjack toads ([i]Bufo calamita[/i])</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1487-09-actual-and-osteochronological-estimated-age-of-natterjack-toads-bufo-calamita?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1487-09-actual-and-osteochronological-estimated-age-of-natterjack-toads-bufo-calamita/file" length="515500" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1487-09-actual-and-osteochronological-estimated-age-of-natterjack-toads-bufo-calamita/file"
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           <media:title type="plain">09. Actual and osteochronological estimated age of natterjack toads ([i]Bufo calamita[/i])</media:title>
           <media:description type="html"><![CDATA[<p>pp.81-82</p>
<p><strong>Authors</strong>:&nbsp;Miguel Tejedo, Ricardo Reques, And Marisa Esteban</p>]]></media:description>
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           <description><![CDATA[<p>pp.81-82</p>
<p><strong>Authors</strong>:&nbsp;Miguel Tejedo, Ricardo Reques, And Marisa Esteban</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:16 +0000</pubDate>
       </item>
              <item>
           <title>08. Behavioural observations of the chameleon [i]Calumma oshaughnessyi oshaughnessyi[/i] in Madagascar</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1486-08-behavioural-observations-of-the-chameleon-calumma-oshaughnessyi-oshaughnessyi-in-madagascar?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1486-08-behavioural-observations-of-the-chameleon-calumma-oshaughnessyi-oshaughnessyi-in-madagascar/file" length="1278749" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1486-08-behavioural-observations-of-the-chameleon-calumma-oshaughnessyi-oshaughnessyi-in-madagascar/file"
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           <media:title type="plain">08. Behavioural observations of the chameleon [i]Calumma oshaughnessyi oshaughnessyi[/i] in Madagascar</media:title>
           <media:description type="html"><![CDATA[<p>pp.77-80</p>
<p><strong>Authors</strong>:&nbsp;J. L. D. Kauffmann, L. D. Brady And R. K. B. Jenkins</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1486-08-behavioural-observations-of-the-chameleon-calumma-oshaughnessyi-oshaughnessyi-in-madagascar?format=html</guid>
           <description><![CDATA[<p>pp.77-80</p>
<p><strong>Authors</strong>:&nbsp;J. L. D. Kauffmann, L. D. Brady And R. K. B. Jenkins</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:15 +0000</pubDate>
       </item>
              <item>
           <title>06. A reassessment of [i]Hardella isoclina[/i] Dubois, 1908 (Testudines: Bataguridae) from the Trinil beds of the Javan Pleistocene</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1484-06-a-reassessment-of-hardella-isoclina-dubois-1908-testudines-bataguridae-from-the-trinil-beds-of-the-javan-pleistocene?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1484-06-a-reassessment-of-hardella-isoclina-dubois-1908-testudines-bataguridae-from-the-trinil-beds-of-the-javan-pleistocene/file" length="436123" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1484-06-a-reassessment-of-hardella-isoclina-dubois-1908-testudines-bataguridae-from-the-trinil-beds-of-the-javan-pleistocene/file"
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           <media:title type="plain">06. A reassessment of [i]Hardella isoclina[/i] Dubois, 1908 (Testudines: Bataguridae) from the Trinil beds of the Javan Pleistocene</media:title>
           <media:description type="html"><![CDATA[<p>pp.71-73</p>
<p><strong>Authors</strong>:&nbsp;Indraneil Das</p>]]></media:description>
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           <description><![CDATA[<p>pp.71-73</p>
<p><strong>Authors</strong>:&nbsp;Indraneil Das</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:14 +0000</pubDate>
       </item>
              <item>
           <title>07. Body temperatures of the Mexican lizard [i]Sceloporus ochoteranae[/i] from two populations in Guerrero, Mexico</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1485-07-body-temperatures-of-the-mexican-lizard-sceloporus-ochoteranae-from-two-populations-in-guerrero-mexico?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1485-07-body-temperatures-of-the-mexican-lizard-sceloporus-ochoteranae-from-two-populations-in-guerrero-mexico/file" length="482631" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1485-07-body-temperatures-of-the-mexican-lizard-sceloporus-ochoteranae-from-two-populations-in-guerrero-mexico/file"
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           <media:title type="plain">07. Body temperatures of the Mexican lizard [i]Sceloporus ochoteranae[/i] from two populations in Guerrero, Mexico</media:title>
           <media:description type="html"><![CDATA[<p>pp.74-76</p>
<p><strong>Authors</strong>:&nbsp;Julio A. Lemos-espinal, Geoffrey R. Smith, And Royce E. Ballinger</p>]]></media:description>
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           <description><![CDATA[<p>pp.74-76</p>
<p><strong>Authors</strong>:&nbsp;Julio A. Lemos-espinal, Geoffrey R. Smith, And Royce E. Ballinger</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:14 +0000</pubDate>
       </item>
              <item>
           <title>05. Notes on the food habits of [i]Coluber hippocrepis nigrescens[/i] from Pantelleria Island a snake that feeds on both carrion and living prey</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1483-05-notes-on-the-food-habits-of-coluber-hippocrepis-nigrescens-from-pantelleria-island-a-snake-that-feeds-on-both-carrion-and-living-prey?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1483-05-notes-on-the-food-habits-of-coluber-hippocrepis-nigrescens-from-pantelleria-island-a-snake-that-feeds-on-both-carrion-and-living-prey/file" length="576216" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1483-05-notes-on-the-food-habits-of-coluber-hippocrepis-nigrescens-from-pantelleria-island-a-snake-that-feeds-on-both-carrion-and-living-prey/file"
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           <media:title type="plain">05. Notes on the food habits of [i]Coluber hippocrepis nigrescens[/i] from Pantelleria Island a snake that feeds on both carrion and living prey</media:title>
           <media:description type="html"><![CDATA[<p>pp.67-70</p>
<p><strong>Authors</strong>:&nbsp;Massimo Capula , Luca Luiselli , Lorenzo Rugiero, Fatima Evangelisti , Claudio Anibaldi And Ve Ronica Trujillo Jesus</p>
<p><strong>Abstract</strong>:&nbsp;The food habits of <em>Coluber hippocrepis nigrescens</em>, a colubrid snake endemic to the island of Pantelleria in the southern Mediterranean Sea, were studied by means of both stomach contents and faecal analyses. Snakes preyed only on vertebrates, and most of the prey eaten were rodents (especially <em>Rattus norvegicus</em>). Ingested biomass per snake averaged 55.63±48.94 g (range: 8 - 131 g), i.e. about 28.5 % of the average snake mass (195.18 ±65.61 g; range: 39-277 g). Log prey mass and log predator mass were positively correlated. The prey mass to predator mass ratio was not significantly correlated with log predator mass. 3 6.36% of the prey found in <em>C. hippocrepis</em> stomachs was eaten by snakes when it was already carrion, as demonstrated by the presence of abundant flesh-fly larvae in rats regurgitated by snakes. This is a very unusual foraging mode for snakes, which are known as active predators feeding on live organisms. We hypothesize that this unusual foraging mode is an adaptive strategy depending on (I) low level of food availability and (2) high abundance of dead prey, on this arid Mediterranean island.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1483-05-notes-on-the-food-habits-of-coluber-hippocrepis-nigrescens-from-pantelleria-island-a-snake-that-feeds-on-both-carrion-and-living-prey?format=html</guid>
           <description><![CDATA[<p>pp.67-70</p>
<p><strong>Authors</strong>:&nbsp;Massimo Capula , Luca Luiselli , Lorenzo Rugiero, Fatima Evangelisti , Claudio Anibaldi And Ve Ronica Trujillo Jesus</p>
<p><strong>Abstract</strong>:&nbsp;The food habits of <em>Coluber hippocrepis nigrescens</em>, a colubrid snake endemic to the island of Pantelleria in the southern Mediterranean Sea, were studied by means of both stomach contents and faecal analyses. Snakes preyed only on vertebrates, and most of the prey eaten were rodents (especially <em>Rattus norvegicus</em>). Ingested biomass per snake averaged 55.63±48.94 g (range: 8 - 131 g), i.e. about 28.5 % of the average snake mass (195.18 ±65.61 g; range: 39-277 g). Log prey mass and log predator mass were positively correlated. The prey mass to predator mass ratio was not significantly correlated with log predator mass. 3 6.36% of the prey found in <em>C. hippocrepis</em> stomachs was eaten by snakes when it was already carrion, as demonstrated by the presence of abundant flesh-fly larvae in rats regurgitated by snakes. This is a very unusual foraging mode for snakes, which are known as active predators feeding on live organisms. We hypothesize that this unusual foraging mode is an adaptive strategy depending on (I) low level of food availability and (2) high abundance of dead prey, on this arid Mediterranean island.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:13 +0000</pubDate>
       </item>
              <item>
           <title>04. On phylogenetic relationships within [i]Dendrotriton[/i] (Amphibia: Caudata: Plethodontidae) is there sufficient evidence</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1482-04-on-phylogenetic-relationships-within-dendrotriton-amphibia-caudata-plethodontidae-is-there-sufficient-evidence?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1482-04-on-phylogenetic-relationships-within-dendrotriton-amphibia-caudata-plethodontidae-is-there-sufficient-evidence/file" length="960497" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1482-04-on-phylogenetic-relationships-within-dendrotriton-amphibia-caudata-plethodontidae-is-there-sufficient-evidence/file"
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           <media:title type="plain">04. On phylogenetic relationships within [i]Dendrotriton[/i] (Amphibia: Caudata: Plethodontidae) is there sufficient evidence</media:title>
           <media:description type="html"><![CDATA[<p>pp.55-65</p>
<p><strong>Authors</strong>:&nbsp;Mark Wilkinson</p>
<p><strong>Abstract</strong>:&nbsp;Previous phylogenetic analyses of the relationships among five Central American salamanders of the genus <em>Dendrotriton</em> are reviewed. The available data was reanalysed using parsimony under a variety of analytical treatments. The results are highly sensitive to (I) the coding method used to convert quantitative characters into discrete character states; (2) different scalings (weighting) of multistate characters; and (3) the omission or inclusion of potentially problematic characters. Explorations of length differences between most parsimonious trees and selected less parsimonious alternatives reveal that under each treatment, most parsimonious trees are only marginally more parsimonious than alternatives and that Bremer support for the clades occurring in MPTs is always low. Tree length distributions are not highly left-skewed as would be expected of phylogenetically informative data. These analyses suggest that there is little phylogenetic signal in the available data and that these data provide little basis for well supported phylogenetic inferences. Both parsimony and compatibility-based randomization tests confirm this interpretation. The null hypotheses that the data are not significantly different from phylogenetically uninformative randomly permuted data cannot be rejected for any of the analytical treatments. Given failure to reject the null hypothesis, phylogenetic hypotheses for <em>Dendrotriton</em> based on the available data are uncompelling. Additional data are needed. Results of the randomization tests are consistent with the view that there has been extensive homoplasy in bolitoglossine salamanders.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1482-04-on-phylogenetic-relationships-within-dendrotriton-amphibia-caudata-plethodontidae-is-there-sufficient-evidence?format=html</guid>
           <description><![CDATA[<p>pp.55-65</p>
<p><strong>Authors</strong>:&nbsp;Mark Wilkinson</p>
<p><strong>Abstract</strong>:&nbsp;Previous phylogenetic analyses of the relationships among five Central American salamanders of the genus <em>Dendrotriton</em> are reviewed. The available data was reanalysed using parsimony under a variety of analytical treatments. The results are highly sensitive to (I) the coding method used to convert quantitative characters into discrete character states; (2) different scalings (weighting) of multistate characters; and (3) the omission or inclusion of potentially problematic characters. Explorations of length differences between most parsimonious trees and selected less parsimonious alternatives reveal that under each treatment, most parsimonious trees are only marginally more parsimonious than alternatives and that Bremer support for the clades occurring in MPTs is always low. Tree length distributions are not highly left-skewed as would be expected of phylogenetically informative data. These analyses suggest that there is little phylogenetic signal in the available data and that these data provide little basis for well supported phylogenetic inferences. Both parsimony and compatibility-based randomization tests confirm this interpretation. The null hypotheses that the data are not significantly different from phylogenetically uninformative randomly permuted data cannot be rejected for any of the analytical treatments. Given failure to reject the null hypothesis, phylogenetic hypotheses for <em>Dendrotriton</em> based on the available data are uncompelling. Additional data are needed. Results of the randomization tests are consistent with the view that there has been extensive homoplasy in bolitoglossine salamanders.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:12 +0000</pubDate>
       </item>
              <item>
           <title>03. Reproductive activity and sexual dimorphism of [i]Liolaemus multimaculatus[/i] (Sauria Tropiduridae)</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1481-03-reproductive-activity-and-sexual-dimorphism-of-liolaemus-multimaculatus-sauria-tropiduridae?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1481-03-reproductive-activity-and-sexual-dimorphism-of-liolaemus-multimaculatus-sauria-tropiduridae/file" length="581236" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1481-03-reproductive-activity-and-sexual-dimorphism-of-liolaemus-multimaculatus-sauria-tropiduridae/file"
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           <media:title type="plain">03. Reproductive activity and sexual dimorphism of [i]Liolaemus multimaculatus[/i] (Sauria Tropiduridae)</media:title>
           <media:description type="html"><![CDATA[<p>pp.49-53</p>
<p><strong>Authors</strong>:&nbsp;Laura E. Vega</p>
<p><strong>Abstract</strong>:&nbsp;The lizard <em>Liolaemus multimaculatus</em> inhabits coastal sand dunes of the Buenos Aires Province of Argentina, and exhibits reproductive activity during the spring and early summer months. Females had vitellogenic follicles and oviductal eggs between September and December, and the size at maturity was 48.2 mm (snout-vent length). Five females with yolked follicles as well as eggs were collected in November, indicating that at least some females can produce more than one clutch per reproductive period. Mean clutch size was 4.2 eggs (range 3 to 7) and clutch size was positively correlated with female body size. In males, testicular diameter pe ked in August (late winter) and September (early summer) and declined in January (mid-summer). Testis size increased gradually from January onwards. Individual males were seen more frequently during the reproductive period than females. Hatchlings were first seen in February and March and the smallest measured 26. 7 mm (snout-vent length). <em>Liolaemus multimaculatus</em> males were larger than females in several morphological traits: snout-vent length, head length, distance between fore and hind limbs, tibio-fibulla, hand and foot lengths.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1481-03-reproductive-activity-and-sexual-dimorphism-of-liolaemus-multimaculatus-sauria-tropiduridae?format=html</guid>
           <description><![CDATA[<p>pp.49-53</p>
<p><strong>Authors</strong>:&nbsp;Laura E. Vega</p>
<p><strong>Abstract</strong>:&nbsp;The lizard <em>Liolaemus multimaculatus</em> inhabits coastal sand dunes of the Buenos Aires Province of Argentina, and exhibits reproductive activity during the spring and early summer months. Females had vitellogenic follicles and oviductal eggs between September and December, and the size at maturity was 48.2 mm (snout-vent length). Five females with yolked follicles as well as eggs were collected in November, indicating that at least some females can produce more than one clutch per reproductive period. Mean clutch size was 4.2 eggs (range 3 to 7) and clutch size was positively correlated with female body size. In males, testicular diameter pe ked in August (late winter) and September (early summer) and declined in January (mid-summer). Testis size increased gradually from January onwards. Individual males were seen more frequently during the reproductive period than females. Hatchlings were first seen in February and March and the smallest measured 26. 7 mm (snout-vent length). <em>Liolaemus multimaculatus</em> males were larger than females in several morphological traits: snout-vent length, head length, distance between fore and hind limbs, tibio-fibulla, hand and foot lengths.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:11 +0000</pubDate>
       </item>
              <item>
           <title>02. Determination of minimum sample size to estimate diet diversity in anuran species</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1480-02-determination-of-minimum-sample-size-to-estimate-diet-diversity-in-anuran-species?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1480-02-determination-of-minimum-sample-size-to-estimate-diet-diversity-in-anuran-species/file" length="613653" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1480-02-determination-of-minimum-sample-size-to-estimate-diet-diversity-in-anuran-species/file"
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           <media:title type="plain">02. Determination of minimum sample size to estimate diet diversity in anuran species</media:title>
           <media:description type="html"><![CDATA[<p>pp.43-47</p>
<p><strong>Authors</strong>:&nbsp;T . Kovacsánd J.Török</p>
<p><strong>Abstract</strong>:&nbsp;Rarefaction analysis was applied to determine the minimum sample size required for any desired degree of accuracy of diet diversity of six anuran species in a particular habitat. This method is suggested for the design of sampling strategies in long-term amphibian studies. In the present study the minimum sample sizes were 28, 36, 32, 1 3 , 24 and 8 for <em>Rana esculenta</em>, <em>R. arvalis</em>, <em>Hyla arborea</em>, <em>Bombina bombina</em>, <em>Pelobates fuscus</em> and <em>Bufo bufo</em>, respectively. The greater the diet diversity of a species, the larger the minimum sample size required, and the smaller the simila ity between individuals within species.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1480-02-determination-of-minimum-sample-size-to-estimate-diet-diversity-in-anuran-species?format=html</guid>
           <description><![CDATA[<p>pp.43-47</p>
<p><strong>Authors</strong>:&nbsp;T . Kovacsánd J.Török</p>
<p><strong>Abstract</strong>:&nbsp;Rarefaction analysis was applied to determine the minimum sample size required for any desired degree of accuracy of diet diversity of six anuran species in a particular habitat. This method is suggested for the design of sampling strategies in long-term amphibian studies. In the present study the minimum sample sizes were 28, 36, 32, 1 3 , 24 and 8 for <em>Rana esculenta</em>, <em>R. arvalis</em>, <em>Hyla arborea</em>, <em>Bombina bombina</em>, <em>Pelobates fuscus</em> and <em>Bufo bufo</em>, respectively. The greater the diet diversity of a species, the larger the minimum sample size required, and the smaller the simila ity between individuals within species.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:10 +0000</pubDate>
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           <title>01. Monitoring a breeding population of crested newts ([i]Triturus cristatus[/i]) in a housing development</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-7-number-2-april-1997/1479-01-monitoring-a-breeding-population-of-crested-newts-triturus-cristatus-in-a-housing-development?format=html</link>
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           <media:title type="plain">01. Monitoring a breeding population of crested newts ([i]Triturus cristatus[/i]) in a housing development</media:title>
           <media:description type="html"><![CDATA[<p>pp.37-41</p>
<p><strong>Authors</strong>:&nbsp;A. S. Cooke</p>
<p><strong>Abstract</strong>:&nbsp;A housing estate was built immediately adjacent to two water bodies utilized by crested newts (<em>Triturus cristatus</em>). Conservation management, particularly pond deepening and fish removal, was undertaken during and after development. This paper describes a monitoring study to determine the success of the operation. Counting adults at night in the breeding season indicated that numbers were at least maintained over a ten year period. Larval counts were made in each of the seven years after the houses were constructed, and more than half of the larvae wer e netted in one year, 1991. In the autumn of 1 990 both ponds were totally dry, and success in 1991 may have been associated with absence offish and low numbers of invertebrate predators. The overall conclusion was that it is possible to conserve crested newts satisfactorily in such a situation.</p>]]></media:description>
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           <description><![CDATA[<p>pp.37-41</p>
<p><strong>Authors</strong>:&nbsp;A. S. Cooke</p>
<p><strong>Abstract</strong>:&nbsp;A housing estate was built immediately adjacent to two water bodies utilized by crested newts (<em>Triturus cristatus</em>). Conservation management, particularly pond deepening and fish removal, was undertaken during and after development. This paper describes a monitoring study to determine the success of the operation. Counting adults at night in the breeding season indicated that numbers were at least maintained over a ten year period. Larval counts were made in each of the seven years after the houses were constructed, and more than half of the larvae wer e netted in one year, 1991. In the autumn of 1 990 both ponds were totally dry, and success in 1991 may have been associated with absence offish and low numbers of invertebrate predators. The overall conclusion was that it is possible to conserve crested newts satisfactorily in such a situation.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:09 +0000</pubDate>
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           <title>Volume 7, Number 2, April 1997 - Full Issue</title>
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           <media:title type="plain">Volume 7, Number 2, April 1997 - Full Issue</media:title>
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           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:08 +0000</pubDate>
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           <title>Table of Contents</title>
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           <media:title type="plain">Table of Contents</media:title>
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           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:07 +0000</pubDate>
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           <title>Front Cover</title>
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           <media:title type="plain">Front Cover</media:title>
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           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 7, Number 2, April 1997</category>
           <pubDate>Fri, 02 Mar 2018 09:52:06 +0000</pubDate>
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