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       <title>Volume 3, Number 1, January 1993 - British Herpetological Society</title>
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       <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993?format=html</link>
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       <url>https://www.thebhs.org/joomlatools-files/docman-images/HJ03-1__Front-Cover.jpg</url>
           <title>Volume 3, Number 1, January 1993 - British Herpetological Society</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993?format=html</link>
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           <title>07. Embryonic and laryal survival of the Common Frog ([i]Rana temporaria[/i] L ) in acidic and limed ponds</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1311-07-embryonic-and-laryal-survival-of-the-common-frog-rana-temporaria-l-in-acidic-and-limed-ponds?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1311-07-embryonic-and-laryal-survival-of-the-common-frog-rana-temporaria-l-in-acidic-and-limed-ponds/file" length="1171871" type="application/pdf" />
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                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1311-07-embryonic-and-laryal-survival-of-the-common-frog-rana-temporaria-l-in-acidic-and-limed-ponds/file"
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           <media:title type="plain">07. Embryonic and laryal survival of the Common Frog ([i]Rana temporaria[/i] L ) in acidic and limed ponds</media:title>
           <media:description type="html"><![CDATA[<p>pp.43-48</p>
<p><strong>Authors</strong>:&nbsp;R. C. Beattie, R. J. Aston And A. G. P. Milner</p>
<p><strong>Abstract</strong>:&nbsp;Limestone was added to two acidic ponds in upland, northern England in an attempt to improve the survival of embryos and larvae of&nbsp;the common frog (<em>Rana temporaria</em> L.). As expected, the addition of limestone to the ponds resulted in a significant increase in both the&nbsp;pH and the dissolved calcium concentration of the pond water. Fertilization success of common frog eggs was approximately 87% in&nbsp;acidic water and increased to I 00% following liming. Embryonic survival in the two acidic ponds increased from 0% and 22% to 69%&nbsp;and 93% respectively following liming. A year after liming, embryonic survival in one pond had decreased significantly from 93% to&nbsp;79%. It was estimated that at least 2. 1 % of the eggs deposited in a limed pond gave rise to metamorphs. The environmental implications&nbsp;of liming acidic frog breeding ponds are discussed.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1311-07-embryonic-and-laryal-survival-of-the-common-frog-rana-temporaria-l-in-acidic-and-limed-ponds?format=html</guid>
           <description><![CDATA[<p>pp.43-48</p>
<p><strong>Authors</strong>:&nbsp;R. C. Beattie, R. J. Aston And A. G. P. Milner</p>
<p><strong>Abstract</strong>:&nbsp;Limestone was added to two acidic ponds in upland, northern England in an attempt to improve the survival of embryos and larvae of&nbsp;the common frog (<em>Rana temporaria</em> L.). As expected, the addition of limestone to the ponds resulted in a significant increase in both the&nbsp;pH and the dissolved calcium concentration of the pond water. Fertilization success of common frog eggs was approximately 87% in&nbsp;acidic water and increased to I 00% following liming. Embryonic survival in the two acidic ponds increased from 0% and 22% to 69%&nbsp;and 93% respectively following liming. A year after liming, embryonic survival in one pond had decreased significantly from 93% to&nbsp;79%. It was estimated that at least 2. 1 % of the eggs deposited in a limed pond gave rise to metamorphs. The environmental implications&nbsp;of liming acidic frog breeding ponds are discussed.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:54 +0000</pubDate>
       </item>
              <item>
           <title>06. Functions of the foam in foam nesting Leptodactylids the nest as a post hatching refuge in [i]Physalaemus pustulosus[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1310-06-functions-of-the-foam-in-foam-nesting-leptodactylids-the-nest-as-a-post-hatching-refuge-in-physalaemus-pustulosus?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1310-06-functions-of-the-foam-in-foam-nesting-leptodactylids-the-nest-as-a-post-hatching-refuge-in-physalaemus-pustulosus/file" length="1300670" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1310-06-functions-of-the-foam-in-foam-nesting-leptodactylids-the-nest-as-a-post-hatching-refuge-in-physalaemus-pustulosus/file"
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           <media:title type="plain">06. Functions of the foam in foam nesting Leptodactylids the nest as a post hatching refuge in [i]Physalaemus pustulosus[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp.35-42</p>
<p><strong>Authors</strong>:&nbsp;J. R. Downie</p>
<p><strong>Abstract</strong>:&nbsp;At 28°C, isolated <em>Physalaemus pusrulosus</em> eggs hatch after approximately 40 hours incubation. However. few tadpoles emerge&nbsp;from foam nests at this time. From nests incubated so that the foam remains moist. emergence occurs progressively over the next&nbsp;day. If the foam is allowed to dry on top, complete emergence takes even longer. Manipulation of the incubation environment shows&nbsp;that emergence is not stimulated by dark or light, nor does it occur at a particular time of day. Since hatching occurs at Gosner stage&nbsp;21 and the last tadpoles to emerge from foam have reached Gosner stage 23-24, it is suggested that late emergence allows hatchlings&nbsp;to continue development to a more advanced stage in a protected environment: the foam acts as a post-hatching refuge. However,&nbsp;it is also shown that tadpoles emerging early are able to grow to Gosner stage 25 by the time the last tadpoles leave the nest: remaining&nbsp;in the nest therefore bears a cost. In addition. part of the delay in emergence may simply result from the time small tadpoles take&nbsp;to wriggle free from a large mass of cohesive foam.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1310-06-functions-of-the-foam-in-foam-nesting-leptodactylids-the-nest-as-a-post-hatching-refuge-in-physalaemus-pustulosus?format=html</guid>
           <description><![CDATA[<p>pp.35-42</p>
<p><strong>Authors</strong>:&nbsp;J. R. Downie</p>
<p><strong>Abstract</strong>:&nbsp;At 28°C, isolated <em>Physalaemus pusrulosus</em> eggs hatch after approximately 40 hours incubation. However. few tadpoles emerge&nbsp;from foam nests at this time. From nests incubated so that the foam remains moist. emergence occurs progressively over the next&nbsp;day. If the foam is allowed to dry on top, complete emergence takes even longer. Manipulation of the incubation environment shows&nbsp;that emergence is not stimulated by dark or light, nor does it occur at a particular time of day. Since hatching occurs at Gosner stage&nbsp;21 and the last tadpoles to emerge from foam have reached Gosner stage 23-24, it is suggested that late emergence allows hatchlings&nbsp;to continue development to a more advanced stage in a protected environment: the foam acts as a post-hatching refuge. However,&nbsp;it is also shown that tadpoles emerging early are able to grow to Gosner stage 25 by the time the last tadpoles leave the nest: remaining&nbsp;in the nest therefore bears a cost. In addition. part of the delay in emergence may simply result from the time small tadpoles take&nbsp;to wriggle free from a large mass of cohesive foam.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:53 +0000</pubDate>
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              <item>
           <title>05. Observations on the reproductive behaviour of the Smith Frog [i]Hyla Jaber[/i]</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1309-05-observations-on-the-reproductive-behaviour-of-the-smith-frog-hyla-jaber?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1309-05-observations-on-the-reproductive-behaviour-of-the-smith-frog-hyla-jaber/file" length="1014367" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1309-05-observations-on-the-reproductive-behaviour-of-the-smith-frog-hyla-jaber/file"
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           <media:title type="plain">05. Observations on the reproductive behaviour of the Smith Frog [i]Hyla Jaber[/i]</media:title>
           <media:description type="html"><![CDATA[<p>pp.31-34&nbsp;</p>
<p><strong>Authors</strong>:&nbsp;Marcio Martins</p>
<p><strong>Abstract</strong>:&nbsp;The reproductive behaviour of the Smith Frog, <em>Hyla Jaber</em>, was studied in an artificial permanent pond in southeastern Brazil.&nbsp;Males. built nests at the edges of this pond where eggs were laid. Reproductive activity continued from late October, 1988 through&nbsp;early March, 1989. Twenty five males and 20 females were marked at the pond. There was no sexual dimorphism in size and females&nbsp;did not choose the larger males. Mean male residency was 15.5 nights; only two females were observed for more than one night.&nbsp;Three different vocalizations were emitted during female attraction and courtship. Courtship behaviour was complex and nearly&nbsp;invariable. Male reproductive success varied between 1 -7 matings and was not correlated with male size, but was positively correlated&nbsp;with length of residency. Only one female was observed mating more than once. Except for minor details, the reproductive&nbsp;behaviour of the Smith Frog is very similar to that observed for <em>Hyla rosenbergi</em>, an ecologically and phylogenetically related species.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1309-05-observations-on-the-reproductive-behaviour-of-the-smith-frog-hyla-jaber?format=html</guid>
           <description><![CDATA[<p>pp.31-34&nbsp;</p>
<p><strong>Authors</strong>:&nbsp;Marcio Martins</p>
<p><strong>Abstract</strong>:&nbsp;The reproductive behaviour of the Smith Frog, <em>Hyla Jaber</em>, was studied in an artificial permanent pond in southeastern Brazil.&nbsp;Males. built nests at the edges of this pond where eggs were laid. Reproductive activity continued from late October, 1988 through&nbsp;early March, 1989. Twenty five males and 20 females were marked at the pond. There was no sexual dimorphism in size and females&nbsp;did not choose the larger males. Mean male residency was 15.5 nights; only two females were observed for more than one night.&nbsp;Three different vocalizations were emitted during female attraction and courtship. Courtship behaviour was complex and nearly&nbsp;invariable. Male reproductive success varied between 1 -7 matings and was not correlated with male size, but was positively correlated&nbsp;with length of residency. Only one female was observed mating more than once. Except for minor details, the reproductive&nbsp;behaviour of the Smith Frog is very similar to that observed for <em>Hyla rosenbergi</em>, an ecologically and phylogenetically related species.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:52 +0000</pubDate>
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              <item>
           <title>03. Individual growth and allometry of young Green Turtles ([i]Chelonia mydas[/i] L )</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1307-03-individual-growth-and-allometry-of-young-green-turtles-chelonia-mydas-l?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1307-03-individual-growth-and-allometry-of-young-green-turtles-chelonia-mydas-l/file" length="1237136" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1307-03-individual-growth-and-allometry-of-young-green-turtles-chelonia-mydas-l/file"
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           <media:title type="plain">03. Individual growth and allometry of young Green Turtles ([i]Chelonia mydas[/i] L )</media:title>
           <media:description type="html"><![CDATA[<p>pp.19-25</p>
<p><strong>Authors</strong>:&nbsp;John Da Yenport And Colin R. Scott</p>
<p><strong>Abstract</strong>:&nbsp;Twelve young green turtles (<em>Chelonia mydas</em> L. ) varied considerably in growth rate when fed satiation rations (mean specific&nbsp;growth rate ranged from 0.01045-0.0l462), but individual animals had constant specific growth rates. The following mean&nbsp;morphometric relationships were found: log y = -3.42 + 2.94 log x (where y = live weight (g) and x = carapace length mm)); log y&nbsp;= 0.069 + 0.93 log x (where y = carapace width (mm) and x = carapace length (mm)); log y = -0. 1 15 + 1 .01 log x (where y = plastron&nbsp;length (mm) and x = carapace length (mm)); log y = -0.417 + 2.04 log x (where y = plastron area (mm2) and x = plastron length&nbsp;(mm)). Growth was isometric throughout the period of study. There was no significant relationship between the allometric coefficients&nbsp;of the individual turtles and their specific growth rates or between carapace length/width ratios and specific growth rates. No&nbsp;turtle shape, or pattern of shape/weight change is associated with high or low rates of specific growth. The plastral scute patterns of&nbsp;green turtles are stable over time and are individually identifiable. Carapace scutes grow asymmetrically, with little posterior or&nbsp;medial growth, most scutal growth taking place anteriorly and laterally. Photocopying of the plastron and scute patterns as a growth/&nbsp;identity technique was shown to be effective and inexpensive.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1307-03-individual-growth-and-allometry-of-young-green-turtles-chelonia-mydas-l?format=html</guid>
           <description><![CDATA[<p>pp.19-25</p>
<p><strong>Authors</strong>:&nbsp;John Da Yenport And Colin R. Scott</p>
<p><strong>Abstract</strong>:&nbsp;Twelve young green turtles (<em>Chelonia mydas</em> L. ) varied considerably in growth rate when fed satiation rations (mean specific&nbsp;growth rate ranged from 0.01045-0.0l462), but individual animals had constant specific growth rates. The following mean&nbsp;morphometric relationships were found: log y = -3.42 + 2.94 log x (where y = live weight (g) and x = carapace length mm)); log y&nbsp;= 0.069 + 0.93 log x (where y = carapace width (mm) and x = carapace length (mm)); log y = -0. 1 15 + 1 .01 log x (where y = plastron&nbsp;length (mm) and x = carapace length (mm)); log y = -0.417 + 2.04 log x (where y = plastron area (mm2) and x = plastron length&nbsp;(mm)). Growth was isometric throughout the period of study. There was no significant relationship between the allometric coefficients&nbsp;of the individual turtles and their specific growth rates or between carapace length/width ratios and specific growth rates. No&nbsp;turtle shape, or pattern of shape/weight change is associated with high or low rates of specific growth. The plastral scute patterns of&nbsp;green turtles are stable over time and are individually identifiable. Carapace scutes grow asymmetrically, with little posterior or&nbsp;medial growth, most scutal growth taking place anteriorly and laterally. Photocopying of the plastron and scute patterns as a growth/&nbsp;identity technique was shown to be effective and inexpensive.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:51 +0000</pubDate>
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              <item>
           <title>04. Individuality of growth, appetite, metabolic rate and assimilation of nutrients in young Green Turtles ([i]Chelonia mydas[/i] L )</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1308-04-individuality-of-growth-appetite-metabolic-rate-and-assimilation-of-nutrients-in-young-green-turtles-chelonia-mydas-l?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1308-04-individuality-of-growth-appetite-metabolic-rate-and-assimilation-of-nutrients-in-young-green-turtles-chelonia-mydas-l/file" length="807044" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1308-04-individuality-of-growth-appetite-metabolic-rate-and-assimilation-of-nutrients-in-young-green-turtles-chelonia-mydas-l/file"
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           <media:title type="plain">04. Individuality of growth, appetite, metabolic rate and assimilation of nutrients in young Green Turtles ([i]Chelonia mydas[/i] L )</media:title>
           <media:description type="html"><![CDATA[<p>pp.26-30</p>
<p><strong>Authors</strong>:&nbsp;John Davenport And Colin R. Scott</p>
<p><strong>Abstract</strong>:&nbsp;Mean appetite and oxygen uptake were highly variable amongst the 12 young green (<em>Chelonia mydas</em> L.) turtles studied. Neither&nbsp;appetite nor oxygen uptake had a statistically significant influence on specific growth rate. Amongst the efficiencies of assimilation&nbsp;of nutrients, there were quite wide individual variations in the rates of assimilation of energy, lipid and dry mass, but protein was&nbsp;assimilated with a uniformly high efficiency. Assimilation efficiencies of lipid and dry mass were significantly and positively correlated&nbsp;with specific growth rate. There were also strong positive correlations between the efficiencies of assimilation of different&nbsp;nutrients. There were weak negative correlations between appetite and the assimilation rates for energy and dry mass. These suggest&nbsp;that turtles compensate for a low efficiency of assimilation of these nutrients by an increased rate of food intake. Lipid assimilation&nbsp;in the turtles was lower than for the other nutrients. It was found that fatty acids are not all absorbed to the same extent. Saturated&nbsp;fatty acids and monounsaturated fatty acids were relatively poorly absorbed by comparison with polyunsaturated fatty acids.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1308-04-individuality-of-growth-appetite-metabolic-rate-and-assimilation-of-nutrients-in-young-green-turtles-chelonia-mydas-l?format=html</guid>
           <description><![CDATA[<p>pp.26-30</p>
<p><strong>Authors</strong>:&nbsp;John Davenport And Colin R. Scott</p>
<p><strong>Abstract</strong>:&nbsp;Mean appetite and oxygen uptake were highly variable amongst the 12 young green (<em>Chelonia mydas</em> L.) turtles studied. Neither&nbsp;appetite nor oxygen uptake had a statistically significant influence on specific growth rate. Amongst the efficiencies of assimilation&nbsp;of nutrients, there were quite wide individual variations in the rates of assimilation of energy, lipid and dry mass, but protein was&nbsp;assimilated with a uniformly high efficiency. Assimilation efficiencies of lipid and dry mass were significantly and positively correlated&nbsp;with specific growth rate. There were also strong positive correlations between the efficiencies of assimilation of different&nbsp;nutrients. There were weak negative correlations between appetite and the assimilation rates for energy and dry mass. These suggest&nbsp;that turtles compensate for a low efficiency of assimilation of these nutrients by an increased rate of food intake. Lipid assimilation&nbsp;in the turtles was lower than for the other nutrients. It was found that fatty acids are not all absorbed to the same extent. Saturated&nbsp;fatty acids and monounsaturated fatty acids were relatively poorly absorbed by comparison with polyunsaturated fatty acids.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:51 +0000</pubDate>
       </item>
              <item>
           <title>02. A review of the genus [i]Lycophidion[/i] (Serpentes Colubridae) in Northeastern Africa</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1306-02-a-review-of-the-genus-lycophidion-serpentes-colubridae-in-northeastern-africa?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1306-02-a-review-of-the-genus-lycophidion-serpentes-colubridae-in-northeastern-africa/file" length="1907114" type="application/pdf" />
           <media:content
                url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1306-02-a-review-of-the-genus-lycophidion-serpentes-colubridae-in-northeastern-africa/file"
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           <media:title type="plain">02. A review of the genus [i]Lycophidion[/i] (Serpentes Colubridae) in Northeastern Africa</media:title>
           <media:description type="html"><![CDATA[<p>pp.8-18</p>
<p><strong>Authors</strong>:&nbsp;Donald G. Broadley And Barry Hughes</p>
<p><strong>Abstract</strong>:&nbsp;Variation in <em>Lycophidion</em> populations of the southern Sudan, Somalia, Ethiopia, Uganda and Kenya is analysed. Five species&nbsp;occur in this area:<em> L. irroraturn</em> and<em> L. ornaturn</em> are restricted to forests, <em>L. depressirostre</em> and<em> L. taylori sp</em>. nov. inhabit dry savannas,&nbsp;<em>L. capense jacksoni</em> is found in the moister savannas of the highlands and plateau areas, while <em>L. capense</em>&nbsp;<em>loveridgei</em> occurs in both&nbsp;forest and savanna of the coastal strip. <em>L. irroraturn</em> is readily distinguished by the paired apical pits on the dorsal scales. <em>L.&nbsp;depressirostre</em> and <em>L. taylori</em> both have lower ventral and subcaudal counts than the other taxa, but <em>L. depressirostre</em> can be distinguished&nbsp;from all other species by its more numerous maxillary teeth (8 to 9 + 19 to 24 compared with 7 to 8 + 11 to 1 8) and usually&nbsp;one colour pattern. <em>L. taylori</em> is very variable in colouration, but most specimens have a white blotch or collar on the nape and white&nbsp;dorsal stippling may be very extensive. The type series of <em>L. taylori</em> comes from the border between northern Somalia and Ethiopia,&nbsp;but there are isolated specimens from northern Kenya (Turkana District), Chad and Senegal.</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1306-02-a-review-of-the-genus-lycophidion-serpentes-colubridae-in-northeastern-africa?format=html</guid>
           <description><![CDATA[<p>pp.8-18</p>
<p><strong>Authors</strong>:&nbsp;Donald G. Broadley And Barry Hughes</p>
<p><strong>Abstract</strong>:&nbsp;Variation in <em>Lycophidion</em> populations of the southern Sudan, Somalia, Ethiopia, Uganda and Kenya is analysed. Five species&nbsp;occur in this area:<em> L. irroraturn</em> and<em> L. ornaturn</em> are restricted to forests, <em>L. depressirostre</em> and<em> L. taylori sp</em>. nov. inhabit dry savannas,&nbsp;<em>L. capense jacksoni</em> is found in the moister savannas of the highlands and plateau areas, while <em>L. capense</em>&nbsp;<em>loveridgei</em> occurs in both&nbsp;forest and savanna of the coastal strip. <em>L. irroraturn</em> is readily distinguished by the paired apical pits on the dorsal scales. <em>L.&nbsp;depressirostre</em> and <em>L. taylori</em> both have lower ventral and subcaudal counts than the other taxa, but <em>L. depressirostre</em> can be distinguished&nbsp;from all other species by its more numerous maxillary teeth (8 to 9 + 19 to 24 compared with 7 to 8 + 11 to 1 8) and usually&nbsp;one colour pattern. <em>L. taylori</em> is very variable in colouration, but most specimens have a white blotch or collar on the nape and white&nbsp;dorsal stippling may be very extensive. The type series of <em>L. taylori</em> comes from the border between northern Somalia and Ethiopia,&nbsp;but there are isolated specimens from northern Kenya (Turkana District), Chad and Senegal.</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:50 +0000</pubDate>
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              <item>
           <title>01. British Quaternary herpetofaunas a history of adaptations to Pleistocene disruptions</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1305-01-british-quaternary-herpetofaunas-a-history-of-adaptations-to-pleistocene-disruptions?format=html</link>
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           <media:title type="plain">01. British Quaternary herpetofaunas a history of adaptations to Pleistocene disruptions</media:title>
           <media:description type="html"><![CDATA[<p>pp.1-7</p>
<p><strong>Authors</strong>:&nbsp;J. Alan Holman</p>
<p><strong>Abstract</strong>:&nbsp;The British Quaternary herpetofauna and the modern one are the products of adaptations to several disruptive patterns. These&nbsp;include mass habitat loss due to glaciation, alternating cold and temperate climates, and the development of seaways isolating the&nbsp;British Islands. Fossil herpetofaunas are now known from all of the Middle and Upper Pleistocene stages (except the Beestonian)&nbsp;and from the Flandrian. The cold stages have yielded only <em>Rana temporaria</em>,<em> Lacerta vivipara</em> and <em>Natrix natrix</em>. The temperate&nbsp;stages have been enriched by exotic continental species incuding: <em>Pelobates fuscus</em>,<em> Pelodytes punctatus</em>, <em>Hyla sp</em>., <em>Rana arvalis</em>,&nbsp;<em>Rana esculenta</em> or<em> ridibunda</em>, <em>Rana lessonae</em>, <em>Emys orbicularis</em>, <em>Elaphe longissima</em>, and <em>Natrix maura</em> or <em>tessellata</em>. Middle&nbsp;Pleistocene Cromerian Interglacial faunas collectively have 38.5% exotic species and Middle Pleistocene Hoxnian Interglacial faunas&nbsp;have 46.5% exotic species. Late Pleistocene Ipswichian (Last Interglacial) faunas have 45.5% exotic species. The only exotic&nbsp;species recorded from the Flandrian (Holocene) is <em>Emys orbicularis</em>. The modern British amphibian fauna must have been in place&nbsp;early in the Flandrian (Holocene), as five of the six modern species occur at the Whitemoor Channel Site, East Cheshire, 1 0,000 to&nbsp;8,500 BP; and there seems no reason to doubt that the modern reptile fauna was also then in place</p>]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1305-01-british-quaternary-herpetofaunas-a-history-of-adaptations-to-pleistocene-disruptions?format=html</guid>
           <description><![CDATA[<p>pp.1-7</p>
<p><strong>Authors</strong>:&nbsp;J. Alan Holman</p>
<p><strong>Abstract</strong>:&nbsp;The British Quaternary herpetofauna and the modern one are the products of adaptations to several disruptive patterns. These&nbsp;include mass habitat loss due to glaciation, alternating cold and temperate climates, and the development of seaways isolating the&nbsp;British Islands. Fossil herpetofaunas are now known from all of the Middle and Upper Pleistocene stages (except the Beestonian)&nbsp;and from the Flandrian. The cold stages have yielded only <em>Rana temporaria</em>,<em> Lacerta vivipara</em> and <em>Natrix natrix</em>. The temperate&nbsp;stages have been enriched by exotic continental species incuding: <em>Pelobates fuscus</em>,<em> Pelodytes punctatus</em>, <em>Hyla sp</em>., <em>Rana arvalis</em>,&nbsp;<em>Rana esculenta</em> or<em> ridibunda</em>, <em>Rana lessonae</em>, <em>Emys orbicularis</em>, <em>Elaphe longissima</em>, and <em>Natrix maura</em> or <em>tessellata</em>. Middle&nbsp;Pleistocene Cromerian Interglacial faunas collectively have 38.5% exotic species and Middle Pleistocene Hoxnian Interglacial faunas&nbsp;have 46.5% exotic species. Late Pleistocene Ipswichian (Last Interglacial) faunas have 45.5% exotic species. The only exotic&nbsp;species recorded from the Flandrian (Holocene) is <em>Emys orbicularis</em>. The modern British amphibian fauna must have been in place&nbsp;early in the Flandrian (Holocene), as five of the six modern species occur at the Whitemoor Channel Site, East Cheshire, 1 0,000 to&nbsp;8,500 BP; and there seems no reason to doubt that the modern reptile fauna was also then in place</p>]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:49 +0000</pubDate>
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           <title>Table of Contents</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1303-table-of-contents-13?format=html</link>
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           <media:title type="plain">Table of Contents</media:title>
           <media:description type="html"><![CDATA[]]></media:description>
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           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:48 +0000</pubDate>
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              <item>
           <title>Volume 3, Number 1, January 1993 - Full Issue</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1304-volume-3-number-1-january-1993-full-issue?format=html</link>
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           <media:title type="plain">Volume 3, Number 1, January 1993 - Full Issue</media:title>
           <media:description type="html"><![CDATA[]]></media:description>
                      <guid isPermaLink="true">https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1304-volume-3-number-1-january-1993-full-issue?format=html</guid>
           <description><![CDATA[]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:48 +0000</pubDate>
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              <item>
           <title>Front Cover</title>
           <link>https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1302-front-cover-21?format=html</link>
           <enclosure url="https://www.thebhs.org/publications/the-herpetological-journal/volume-3-number-1-january-1993/1302-front-cover-21/file" length="364698" type="application/pdf" />
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           <media:title type="plain">Front Cover</media:title>
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           <description><![CDATA[]]></description>
           <author>webmaster@ayeayedesign.co.uk (Jen Drage)</author>
           <category>Volume 3, Number 1, January 1993</category>
           <pubDate>Thu, 01 Mar 2018 20:58:47 +0000</pubDate>
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