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rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00545.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00546.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00548.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00549.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12026"/></rdf:Seq></items></channel><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12036" xmlns="http://purl.org/rss/1.0/"><title>Co-evolution of gametes of the Greater Bandicoot Rat, Bandicota indica – a murine rodent from South-East Asia</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12036</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Co-evolution of gametes of the Greater Bandicoot Rat, Bandicota indica – a murine rodent from South-East Asia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fiona Dorman, Priscilla Balsamo, Chris Leigh, William G. Breed</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T00:37:12.565989-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12036</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12036</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12036</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Most Old World mice and rats, subfamily Murinae, have a spermatozoon with an apical hook, a long tail and, as seen typically in eutherian mammals, a bilaterally flattened head. Dramatically different from this are the sperm of the Greater Bandicoot Rat, <em>Bandicota indica</em>. Here, we ask the question has the structure of the sperm head co-evolved with that of the egg coat, the zona pellucida? For this, we first summarise the morphological features of the spermatozoon of <em>B. indica</em> that may relate to zona pellucida penetration at the time of fertilisation, and we confirm that the sperm head is generally round, not bilaterally flattened, in profile and has a huge acrosome. We then show that the zona pellucida around oocytes in tertiary follicles also differs from that of the other murine rodents in being only about 4 μm thick and, as demonstrated by lectin staining, has an unusual abundance of alpha-L-fucose. These findings indicate that both the male and female gametes of this South-East Asian murine rodent are highly divergent in their structural organisation. One of the functional implications of this probably relates to sperm–zona interactions and the release of acrosomal enzymes that probably facilitate penetration by digestion of the zona matrix at the time of fertilisation.</p></div>
]]></content:encoded><description>

Most Old World mice and rats, subfamily Murinae, have a spermatozoon with an apical hook, a long tail and, as seen typically in eutherian mammals, a bilaterally flattened head. Dramatically different from this are the sperm of the Greater Bandicoot Rat, Bandicota indica. Here, we ask the question has the structure of the sperm head co-evolved with that of the egg coat, the zona pellucida? For this, we first summarise the morphological features of the spermatozoon of B. indica that may relate to zona pellucida penetration at the time of fertilisation, and we confirm that the sperm head is generally round, not bilaterally flattened, in profile and has a huge acrosome. We then show that the zona pellucida around oocytes in tertiary follicles also differs from that of the other murine rodents in being only about 4 μm thick and, as demonstrated by lectin staining, has an unusual abundance of alpha-L-fucose. These findings indicate that both the male and female gametes of this South-East Asian murine rodent are highly divergent in their structural organisation. One of the functional implications of this probably relates to sperm–zona interactions and the release of acrosomal enzymes that probably facilitate penetration by digestion of the zona matrix at the time of fertilisation.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12035" xmlns="http://purl.org/rss/1.0/"><title>Underwater sound emission as part of an antipredator mechanism in Ceratophrys cranwelli tadpoles</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12035</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Underwater sound emission as part of an antipredator mechanism in Ceratophrys cranwelli tadpoles</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carolina Salgado Costa, Mariana Chuliver Pereyra, Leandro Alcalde, Raúl Herrera, Vance L. Trudeau, Guillermo S. Natale</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-12T20:49:42.181073-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12035</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12035</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12035</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We report the emission of underwater sounds in the tadpoles of a second member of the family Ceratophryidae, <em>Ceratophrys cranwelli</em>. These tadpoles produce a short metallic-like sound, which consists of short trains of pulses at Gosner stages 25, 28, and 37. Experiment I was designed to record underwater sounds and their characteristics. Experiment II was designed to test: (i) if at higher densities (total number of tadpoles/L) but fixed predator–prey proportions <em>C. cranwelli</em> larvae are cannibalistic, (ii) if cannibalism increases at higher proportions of predators at a fixed density, and (iii) if tadpoles display a mechanism of intraspecific recognition that may diminish the frequency of cannibalism. Each treatment combines larvae of <em>C. cranwelli</em> (predator) with those of <em>Rhinella arenarum</em> (prey). The number of live and dead individuals was recorded during 72 h, and the following variables were calculated: time to eat the first and second prey, time without eating, time to eat a congener, and number of events of cannibalism. The results indicate that relative predator–prey availability affects the frequency of predation between conspecifics. We consider that an antipredator mechanism exists in <em>C. cranwelli</em> tadpoles and that the underwater sound is part of it.</p></div>
]]></content:encoded><description>

We report the emission of underwater sounds in the tadpoles of a second member of the family Ceratophryidae, Ceratophrys cranwelli. These tadpoles produce a short metallic-like sound, which consists of short trains of pulses at Gosner stages 25, 28, and 37. Experiment I was designed to record underwater sounds and their characteristics. Experiment II was designed to test: (i) if at higher densities (total number of tadpoles/L) but fixed predator–prey proportions C. cranwelli larvae are cannibalistic, (ii) if cannibalism increases at higher proportions of predators at a fixed density, and (iii) if tadpoles display a mechanism of intraspecific recognition that may diminish the frequency of cannibalism. Each treatment combines larvae of C. cranwelli (predator) with those of Rhinella arenarum (prey). The number of live and dead individuals was recorded during 72 h, and the following variables were calculated: time to eat the first and second prey, time without eating, time to eat a congener, and number of events of cannibalism. The results indicate that relative predator–prey availability affects the frequency of predation between conspecifics. We consider that an antipredator mechanism exists in C. cranwelli tadpoles and that the underwater sound is part of it.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12033" xmlns="http://purl.org/rss/1.0/"><title>Anatomy of the fully formed chondrocranium of Podocnemis unifilis (Pleurodira: Podocnemididae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12033</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Anatomy of the fully formed chondrocranium of Podocnemis unifilis (Pleurodira: Podocnemididae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christopher A. Sheil, Krista Zaharewicz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-08T20:42:49.915094-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12033</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12033</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12033</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study describes the anatomy of the chondrocranium of <em>Podocnemis unifilis</em> (Pleurodira, Podocnemididae), based on recently hatched specimens, and cleared and double-stained specimens. The orbitotemporal region is dramatically different from those observed for other species of turtles in that the: (1) planum supraseptale is greatly reduced and present only as tiny projections on the posterodorsal margin of the interorbital septum, (2) pila metoptica is free from all neighbouring structures and bifurcates distally, (3) pila antotica is greatly reduced, (4) foramina for optic nerve, ophthalmic artery and oculomotor nerves are open dorsally by virtue of this species lacking the taenia marginalis and taenia medialis, and (5) tectum synoticum is present and invested dorsally by the supraoccipital, despite the fact that this bone forms by replacement of the supraoccipital. The unique morphology of the pila metoptica is explained either as <em>de novo</em> formation of processes on the terminus of this cartilage or by retention of portions of the taenia medialis (anteriorly) and pila antotica or pila accessoria (posteriorly). Variation in the orbitotemporal region presented here is discussed for two other pleurodiran turtles (<em>Phrynops hilarii</em> and <em>Emydura subglobosa</em>) and briefly compared with the anatomy observed in Cryptodira.</p></div>
]]></content:encoded><description>

This study describes the anatomy of the chondrocranium of Podocnemis unifilis (Pleurodira, Podocnemididae), based on recently hatched specimens, and cleared and double-stained specimens. The orbitotemporal region is dramatically different from those observed for other species of turtles in that the: (1) planum supraseptale is greatly reduced and present only as tiny projections on the posterodorsal margin of the interorbital septum, (2) pila metoptica is free from all neighbouring structures and bifurcates distally, (3) pila antotica is greatly reduced, (4) foramina for optic nerve, ophthalmic artery and oculomotor nerves are open dorsally by virtue of this species lacking the taenia marginalis and taenia medialis, and (5) tectum synoticum is present and invested dorsally by the supraoccipital, despite the fact that this bone forms by replacement of the supraoccipital. The unique morphology of the pila metoptica is explained either as de novo formation of processes on the terminus of this cartilage or by retention of portions of the taenia medialis (anteriorly) and pila antotica or pila accessoria (posteriorly). Variation in the orbitotemporal region presented here is discussed for two other pleurodiran turtles (Phrynops hilarii and Emydura subglobosa) and briefly compared with the anatomy observed in Cryptodira.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12034" xmlns="http://purl.org/rss/1.0/"><title>The haemocytes of the salp Thalia democratica (Tunicata, Thaliacea): an ultrastructural and histochemical study in the oozoid</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12034</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The haemocytes of the salp Thalia democratica (Tunicata, Thaliacea): an ultrastructural and histochemical study in the oozoid</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Francesca Cima, Federico Caicci, Paolo Sordino</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-08T20:42:30.165491-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12034</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12034</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12034</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In comparative immunology and evolution of the chordate immune system, tunicates hold an important phylogenetic position as sister group of vertebrates. However, knowledge of the tunicate immune system is limited to the class Ascidiacea, in which some species are now considered model organisms. In the class Thaliacea, represented by fragile pelagic species, the few studies on their haemocytes go back to several decades ago and do not consider comparative aspects with ascidian haemocytes. In this study, we identified various haemocyte types and their distribution in the common salp <em>Thalia democratica</em> by comparative observations under light and electron microscopy and by histochemical, histoenzymatic and immunohistochemical techniques. By comparing specialisations with those of ascidian haemocytes, we detected an undifferentiated cell type (lymphocyte-like cell) and three categories with four cell types, that is, (i) phagocytic line (hyaline amoebocyte and amoebocyte with large vacuoles), (ii) mast cell-like line (granular cell) and (iii) storage cells (nephrocyte). Both phagocytes and granular cells appear to migrate in the tunic. Phagocytes adhere to the tunic which internally covers the oral siphon, where they probably function as sentinel cells of the pharynx. Results show the variety of haemolymph cells in the salp similar to phlebobranch ascidians.</p></div>
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In comparative immunology and evolution of the chordate immune system, tunicates hold an important phylogenetic position as sister group of vertebrates. However, knowledge of the tunicate immune system is limited to the class Ascidiacea, in which some species are now considered model organisms. In the class Thaliacea, represented by fragile pelagic species, the few studies on their haemocytes go back to several decades ago and do not consider comparative aspects with ascidian haemocytes. In this study, we identified various haemocyte types and their distribution in the common salp Thalia democratica by comparative observations under light and electron microscopy and by histochemical, histoenzymatic and immunohistochemical techniques. By comparing specialisations with those of ascidian haemocytes, we detected an undifferentiated cell type (lymphocyte-like cell) and three categories with four cell types, that is, (i) phagocytic line (hyaline amoebocyte and amoebocyte with large vacuoles), (ii) mast cell-like line (granular cell) and (iii) storage cells (nephrocyte). Both phagocytes and granular cells appear to migrate in the tunic. Phagocytes adhere to the tunic which internally covers the oral siphon, where they probably function as sentinel cells of the pharynx. Results show the variety of haemolymph cells in the salp similar to phlebobranch ascidians.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12032" xmlns="http://purl.org/rss/1.0/"><title>Comparative description of the hairy structures in two endemic Velia species (Insecta: Hemiptera: Heteroptera: Veliidae): V. currens (Fabricius, 1794) and V. gridellii Tamanini, 1947</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12032</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparative description of the hairy structures in two endemic Velia species (Insecta: Hemiptera: Heteroptera: Veliidae): V. currens (Fabricius, 1794) and V. gridellii Tamanini, 1947</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fabio Cianferoni, Giacomo Santini</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-26T01:10:47.597035-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12032</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12032</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12032</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study provides the first description, based on SEM imagery, of the hairy structures related to life on the water surface of two Alpine-Apenninic species belonging to the genus <em>Velia</em>:<em> V. currens</em> (Fabricius, 1794) and <em>V. gridellii</em> Tamanini, 1947. In general, no relevant differences in the organization and form of these structures were found between the two species. Similarly, few differences were observed between males and females, and in comparison with the only congeneric with hairy structures thus far described, <em>V. caprai</em> Tamanini, 1947, confirming a substantial homogeneity within the subgenus <em>Plesiovelia</em>. The discovery of a double layer of microtrichia in both our species allowed us to detect them even in <em>V. caprai</em>, for which only a single layer was previously described. Finally, the presence of a structure corresponding to the male grasping comb was discovered in females of <em>V. gridellii</em> and is reported for the first time in the genus and in the Old World Veliinae. A similar structure was not identified in <em>V. currens</em>. This difference may be relevant for better understanding the relationships among species belonging to this genus.</p></div>
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This study provides the first description, based on SEM imagery, of the hairy structures related to life on the water surface of two Alpine-Apenninic species belonging to the genus Velia: V. currens (Fabricius, 1794) and V. gridellii Tamanini, 1947. In general, no relevant differences in the organization and form of these structures were found between the two species. Similarly, few differences were observed between males and females, and in comparison with the only congeneric with hairy structures thus far described, V. caprai Tamanini, 1947, confirming a substantial homogeneity within the subgenus Plesiovelia. The discovery of a double layer of microtrichia in both our species allowed us to detect them even in V. caprai, for which only a single layer was previously described. Finally, the presence of a structure corresponding to the male grasping comb was discovered in females of V. gridellii and is reported for the first time in the genus and in the Old World Veliinae. A similar structure was not identified in V. currens. This difference may be relevant for better understanding the relationships among species belonging to this genus.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12031" xmlns="http://purl.org/rss/1.0/"><title>Morphological adaptations to arboreal habitats and heart position in species of the neotropical whipsnakes genus Chironius</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12031</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Morphological adaptations to arboreal habitats and heart position in species of the neotropical whipsnakes genus Chironius</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Murilo Guimarães, Marília P. Gaiarsa, Hamanda B. Cavalheri</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-02T01:16:43.658809-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12031</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12031</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12031</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The evolution of arboreality in snakes is accompanied by modifications that are remarkably similar across species. Gravity is one of the most important selective agents, and arboreal snakes present adaptations to circumvent the gradient of pressure, including modifications on heart position (HP) and body slenderness (BS). However, the degree to which different life-history traits influence the cardiovascular system of snakes remains unclear. Here, we used an ecological and a phylogenetic approach to explore the relationship between habitat, HP, BS, and heart size (HS) in five species of the neotropical whipsnakes genus <em>Chironius</em> that occupy terrestrial, semiarboreal, and arboreal habits. Our ecological comparison indicated that the arboreal species have the most posterior-positioned heart, the most slender body, and the smallest HS, whereas the terrestrial representative of the group exhibited the most anterior heart, the less flattened body, and the largest HS. After removing the phylogenetic effect, we found no difference in HP and BS between terrestrial and arboreal species. Habitat only differed when contrasting with HS. Body slenderness and HS were correlated with HP. Our results suggest that different restrictions, such as anatomical constraints, behavior, and phylogenetic inertia, may be important for the studied species.</p></div>
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The evolution of arboreality in snakes is accompanied by modifications that are remarkably similar across species. Gravity is one of the most important selective agents, and arboreal snakes present adaptations to circumvent the gradient of pressure, including modifications on heart position (HP) and body slenderness (BS). However, the degree to which different life-history traits influence the cardiovascular system of snakes remains unclear. Here, we used an ecological and a phylogenetic approach to explore the relationship between habitat, HP, BS, and heart size (HS) in five species of the neotropical whipsnakes genus Chironius that occupy terrestrial, semiarboreal, and arboreal habits. Our ecological comparison indicated that the arboreal species have the most posterior-positioned heart, the most slender body, and the smallest HS, whereas the terrestrial representative of the group exhibited the most anterior heart, the less flattened body, and the largest HS. After removing the phylogenetic effect, we found no difference in HP and BS between terrestrial and arboreal species. Habitat only differed when contrasting with HS. Body slenderness and HS were correlated with HP. Our results suggest that different restrictions, such as anatomical constraints, behavior, and phylogenetic inertia, may be important for the studied species.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12027" xmlns="http://purl.org/rss/1.0/"><title>Adaptive morphology of the heart of Southern-Fur-Seal (Arctocephalus australis – Zimmermamm, 1783)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12027</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Adaptive morphology of the heart of Southern-Fur-Seal (Arctocephalus australis – Zimmermamm, 1783)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Juliana P. Guimarães, Renata B. Mari, Alfredo Bas, Ii-Sei Watanabe</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-21T02:47:18.065989-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12027</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12027</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12027</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The Southern-fur-seal belongs to the order Carnivora, suborder Pinnipedia, and Otariidae family. This species inhabits aquatic and terrestrial environments, thus presenting important morphophysiological adaptive changes, especially in the cardiac system. For this purpose, Southern-fur-seal (<em>Arctocephalus australis</em>) hearts were used from animals that died from natural causes. Gross morphology observations were supported by light, scanning and transmission electron microscopy. The heart was long and flat; it was lined by pericardium and partly covered by lungs. Structurally, atrium and ventricle muscle fibers exhibit typical features of cardiac fibers revealing myofibrils bundles, mitochondria, plate-shaped junctions, anastomosis between myofibrils bundles, and electron-dense granule natriuretic around the nucleus and mitochondria of atrium muscle cells. The Southern-fur-seal heart was structurally similar to other mammals; however, it presented morphological changes that assist in their adaptation to their environment.</p></div>
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The Southern-fur-seal belongs to the order Carnivora, suborder Pinnipedia, and Otariidae family. This species inhabits aquatic and terrestrial environments, thus presenting important morphophysiological adaptive changes, especially in the cardiac system. For this purpose, Southern-fur-seal (Arctocephalus australis) hearts were used from animals that died from natural causes. Gross morphology observations were supported by light, scanning and transmission electron microscopy. The heart was long and flat; it was lined by pericardium and partly covered by lungs. Structurally, atrium and ventricle muscle fibers exhibit typical features of cardiac fibers revealing myofibrils bundles, mitochondria, plate-shaped junctions, anastomosis between myofibrils bundles, and electron-dense granule natriuretic around the nucleus and mitochondria of atrium muscle cells. The Southern-fur-seal heart was structurally similar to other mammals; however, it presented morphological changes that assist in their adaptation to their environment.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12030" xmlns="http://purl.org/rss/1.0/"><title>Immunocytochemistry indicates that glycine-rich beta-proteins are present in the beta-layer, while cysteine-rich beta-proteins are present in beta- and alpha-layers of snake epidermis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12030</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Immunocytochemistry indicates that glycine-rich beta-proteins are present in the beta-layer, while cysteine-rich beta-proteins are present in beta- and alpha-layers of snake epidermis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lorenzo Alibardi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-19T21:00:55.029639-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12030</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12030</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12030</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Immunolocalization of glycine-rich and cysteine–glycine-medium-rich beta-proteins (Beta-keratins) in snake epidermis indicates a different distribution between beta- and alpha-layers. Acta Zoologica, Stockholm. The epidermis of snakes consists of hard beta-keratin layers alternated with softer and pliable alpha-keratin layers. Using Western blot, light and ultrastructural immunolocalization, we have analyzed the distribution of two specific beta-proteins (formerly beta-keratins) in the epidermis of snakes. The study indicates that the antibody HgG5, recognizing glycine-rich beta-proteins of 12–15 kDa, is poorly or not reactive with the beta-layer of snake epidermis. This suggests that glycine-rich proteins similar to those present in lizards are altered during maturation of the beta-layer. Conversely, a glycine–cysteine-medium-rich beta-protein (HgGC10) of 10–12 kDa is present in beta- and alpha-layers, but it is reduced or disappears in precorneous and suprabasal cells destined to give rise to beta- and alpha-cells. Together with the previous studies on reptilian epidermis, the present results suggest that beta-proteins rich in glycine mainly accumulate on a scaffold of alpha-keratin producing a resistant and hydrophobic beta-layer. Conversely, beta-proteins lower in glycine but higher in cysteine accumulate on alpha-keratin filaments present in beta- and alpha-layers producing resistant but more pliable layers.</p></div>
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Immunolocalization of glycine-rich and cysteine–glycine-medium-rich beta-proteins (Beta-keratins) in snake epidermis indicates a different distribution between beta- and alpha-layers. Acta Zoologica, Stockholm. The epidermis of snakes consists of hard beta-keratin layers alternated with softer and pliable alpha-keratin layers. Using Western blot, light and ultrastructural immunolocalization, we have analyzed the distribution of two specific beta-proteins (formerly beta-keratins) in the epidermis of snakes. The study indicates that the antibody HgG5, recognizing glycine-rich beta-proteins of 12–15 kDa, is poorly or not reactive with the beta-layer of snake epidermis. This suggests that glycine-rich proteins similar to those present in lizards are altered during maturation of the beta-layer. Conversely, a glycine–cysteine-medium-rich beta-protein (HgGC10) of 10–12 kDa is present in beta- and alpha-layers, but it is reduced or disappears in precorneous and suprabasal cells destined to give rise to beta- and alpha-cells. Together with the previous studies on reptilian epidermis, the present results suggest that beta-proteins rich in glycine mainly accumulate on a scaffold of alpha-keratin producing a resistant and hydrophobic beta-layer. Conversely, beta-proteins lower in glycine but higher in cysteine accumulate on alpha-keratin filaments present in beta- and alpha-layers producing resistant but more pliable layers.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12029" xmlns="http://purl.org/rss/1.0/"><title>Green fluorescent protein (GFP) expression patterns in the olfactory epithelium of GFP transgenic cloned Jinhua pigs</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12029</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Green fluorescent protein (GFP) expression patterns in the olfactory epithelium of GFP transgenic cloned Jinhua pigs</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Atsushi Hirao, Tatsuo Kawarasaki, Kenjiro Konno, Satoko Enya, Masatoshi Shibata, Akihisa Kangawa, Eiji Kobayashi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-19T21:00:30.628976-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12029</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12029</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12029</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Domestic pigs possess a well-developed sense of smell. However, the morphology of the porcine olfactory epithelium (OE) is poorly understood. Recently, several strains of transgenic cloned pigs that are presumed to ubiquitously express green fluorescent protein (GFP) have been created. Thus, the purpose of this study was to elucidate the features of porcine OE using the tissues of GFP transgenic cloned pigs. Based on observations of Hematoxylin and Eosin staining and measurements of thickness, porcine OE tissue portions were classified into three categories (thick, standard, and thin). Cryosections revealed that the prominent GFP signals were expressed in olfactory sensory neurons (OSN), Bowman's glands, and olfactory nerve. A few GFP-expressing sustentacular cells were seen; however, the intensity of GFP fluorescence was slight. In the thick portion, numerous GFP-expressing polygonal OSN that did not possess dendrites were found. In the standard portions, GFP-expressing cells had longitudinal dendrites. A few GFP-expressing cells were found in the thin portion. In the thick and standard portions, most of the prominent GFP-expressing cells were positive for olfactory marker protein. Moreover, double immunofluorescence staining with boiled GFP and Sox2 antibody revealed that GFP expression patterns in OSN are synchronized with Sox2 immunoreactive patterns.</p></div>
]]></content:encoded><description>

Domestic pigs possess a well-developed sense of smell. However, the morphology of the porcine olfactory epithelium (OE) is poorly understood. Recently, several strains of transgenic cloned pigs that are presumed to ubiquitously express green fluorescent protein (GFP) have been created. Thus, the purpose of this study was to elucidate the features of porcine OE using the tissues of GFP transgenic cloned pigs. Based on observations of Hematoxylin and Eosin staining and measurements of thickness, porcine OE tissue portions were classified into three categories (thick, standard, and thin). Cryosections revealed that the prominent GFP signals were expressed in olfactory sensory neurons (OSN), Bowman's glands, and olfactory nerve. A few GFP-expressing sustentacular cells were seen; however, the intensity of GFP fluorescence was slight. In the thick portion, numerous GFP-expressing polygonal OSN that did not possess dendrites were found. In the standard portions, GFP-expressing cells had longitudinal dendrites. A few GFP-expressing cells were found in the thin portion. In the thick and standard portions, most of the prominent GFP-expressing cells were positive for olfactory marker protein. Moreover, double immunofluorescence staining with boiled GFP and Sox2 antibody revealed that GFP expression patterns in OSN are synchronized with Sox2 immunoreactive patterns.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12028" xmlns="http://purl.org/rss/1.0/"><title>Between a rock and a soft place: microtopography of the locomotor substrate and the morphology of the setal fields of Namibian day geckos (Gekkota: Gekkonidae: Rhoptropus)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12028</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Between a rock and a soft place: microtopography of the locomotor substrate and the morphology of the setal fields of Namibian day geckos (Gekkota: Gekkonidae: Rhoptropus)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anthony P. Russell, Megan K. Johnson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-15T02:58:25.196514-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12028</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12028</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12028</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Many species of gekkotans possess adhesive subdigital pads that allow them to adhere to, and move on, a wide variety of surfaces. The natural surfaces exploited by these lizards may be rough, undulant and unpredictable and therefore likely provide only limited, patchy areas for adhesive contact. Here, we examine the microtopography of rock surfaces used by seven species of <em>Rhoptropus</em> and compare this to several rough and smooth artificial surfaces employed in previous studies of gekkotan adhesion. These data are considered in relation to the form, configuration, compliance and functional morphology of the setal fields of these species. Our results demonstrate that natural rock surfaces are rough and unpredictable at the scale of the setal arrays, with equal amounts of variation existing within and between the various types of rock surfaces examined. Such surfaces differ from smooth and rough artificial surfaces in the proportion of surface area available for attachment and the relative predictability of surface undulance. Generally, setal field characteristics of individual species are not relatable to specific substrates, but instead are configured to allow for sufficient attachment to a wide variety of unpredictable surfaces. Our findings provide insight into the evolution and microanatomy of the adhesive system of gekkotan lizards and its adaptive relationship to topographically unpredictable surfaces.</p></div>
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Many species of gekkotans possess adhesive subdigital pads that allow them to adhere to, and move on, a wide variety of surfaces. The natural surfaces exploited by these lizards may be rough, undulant and unpredictable and therefore likely provide only limited, patchy areas for adhesive contact. Here, we examine the microtopography of rock surfaces used by seven species of Rhoptropus and compare this to several rough and smooth artificial surfaces employed in previous studies of gekkotan adhesion. These data are considered in relation to the form, configuration, compliance and functional morphology of the setal fields of these species. Our results demonstrate that natural rock surfaces are rough and unpredictable at the scale of the setal arrays, with equal amounts of variation existing within and between the various types of rock surfaces examined. Such surfaces differ from smooth and rough artificial surfaces in the proportion of surface area available for attachment and the relative predictability of surface undulance. Generally, setal field characteristics of individual species are not relatable to specific substrates, but instead are configured to allow for sufficient attachment to a wide variety of unpredictable surfaces. Our findings provide insight into the evolution and microanatomy of the adhesive system of gekkotan lizards and its adaptive relationship to topographically unpredictable surfaces.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12025" xmlns="http://purl.org/rss/1.0/"><title>Microvascular anatomy and histomorphology of extrapulmonary bronchi in adult Xenopus laevis Daudin (Lissamphibia; Anura) point to a role in aerial gas exchange – histomorphology of tissue sections and scanning electron microscopy of vascular corrosion casts</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12025</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Microvascular anatomy and histomorphology of extrapulmonary bronchi in adult Xenopus laevis Daudin (Lissamphibia; Anura) point to a role in aerial gas exchange – histomorphology of tissue sections and scanning electron microscopy of vascular corrosion casts</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wasan Tangphokhanon, Alois Lametschwandtner</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-15T00:06:00.955652-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12025</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12025</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12025</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Studies on the amphibian respiratory tract microvascular anatomy are few. Using scanning electron microscopy (SEM) of vascular corrosion casts (VCCs) and light microscopy of perfusion-fixed tissue sections, we studied the bronchial microvascular anatomy in the adult South African Clawed Toad, <em>Xenopus laevis </em>Daudin. Histomorphology showed that the bronchial wall consists (from luminal to abluminal) of squamous epithelium, subepithelial capillary bed, cartilage rings or cartilage plates, a layer of dense connective tissue, a layer of smooth muscle cells, and squamous epithelium (serosa). SEM of VCCs reveals that bilaterally a ventral, a dorsal (Ø 77.21 ± 7.61 μm), and a caudal bronchial artery supply the bronchial subepithelial capillary bed. The ventral bronchial artery has 3–4 branching orders (interbranching distances: 506.3 ± 392.12 μm; branching angles of first- and second-order bifurcations: 24.60 ± 10.24° and 29.59 ± 14.3°). Casts of bronchial arteries display imprints of flow dividers and sphincters. Cranial and caudal bronchial veins (Ø 154.78 ± 49.68 μm) drain into pulmonary veins. They lack microvenous valves. The location of the dense subepithelial capillary meshwork just beneath the thin squamous bronchial epithelium and its drainage into the pulmonary veins make it likely that in <em>Xenopus,</em> bronchi assist in aerial gas exchange.</p></div>
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Studies on the amphibian respiratory tract microvascular anatomy are few. Using scanning electron microscopy (SEM) of vascular corrosion casts (VCCs) and light microscopy of perfusion-fixed tissue sections, we studied the bronchial microvascular anatomy in the adult South African Clawed Toad, Xenopus laevis Daudin. Histomorphology showed that the bronchial wall consists (from luminal to abluminal) of squamous epithelium, subepithelial capillary bed, cartilage rings or cartilage plates, a layer of dense connective tissue, a layer of smooth muscle cells, and squamous epithelium (serosa). SEM of VCCs reveals that bilaterally a ventral, a dorsal (Ø 77.21 ± 7.61 μm), and a caudal bronchial artery supply the bronchial subepithelial capillary bed. The ventral bronchial artery has 3–4 branching orders (interbranching distances: 506.3 ± 392.12 μm; branching angles of first- and second-order bifurcations: 24.60 ± 10.24° and 29.59 ± 14.3°). Casts of bronchial arteries display imprints of flow dividers and sphincters. Cranial and caudal bronchial veins (Ø 154.78 ± 49.68 μm) drain into pulmonary veins. They lack microvenous valves. The location of the dense subepithelial capillary meshwork just beneath the thin squamous bronchial epithelium and its drainage into the pulmonary veins make it likely that in Xenopus, bronchi assist in aerial gas exchange.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12023" xmlns="http://purl.org/rss/1.0/"><title>Pattern of serotonin-like immunoreactive cells in scyphozoan and hydrozoan planulae and their relation to settlement</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12023</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Pattern of serotonin-like immunoreactive cells in scyphozoan and hydrozoan planulae and their relation to settlement</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tatiana Mayorova, Jacob Kach, Igor Kosevich</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-14T01:21:51.243302-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12023</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12023</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12023</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The planulae of almost all investigated cnidarian species possess neuron-like cells. The distribution of these cells is usually uneven throughout the long axis of the planula. The majority of these cells are located in the anterior half of the planula body. Scyphozoan planulae, as well as anthozoan planulae, have a sensory structure at the anterior pole called an apical organ, which is believed to take part in metamorphosis induction. Hydrozoan planulae also possess sensory cells. It has been previously shown in several cnidarian larvae that their neuronal cells contain the neurotransmitter, serotonin. The present study describes the peculiarities of serotonin-like immunoreactive cells in <em>Aurelia aurita</em> (Scyphozoa) and <em>Gonothyraea loveni</em> (Hydrozoa) planulae. We show that several cells in the presumptive apical organ of <em>A. aurita</em> are immunoreactive to antibodies against serotonin, while <em>G. loveni</em> planulae have an accumulation of serotonin-positive cells near the anterior pole. Additional serotonin-like immunoreactive cells are found in the lateral ectoderm of both planulae. Treatment of <em>A. aurita</em> and <em>G. loveni</em> planulae with serotonin or its blockers show that serotonin is likely involved in the initiation of planula settlement.</p></div>
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The planulae of almost all investigated cnidarian species possess neuron-like cells. The distribution of these cells is usually uneven throughout the long axis of the planula. The majority of these cells are located in the anterior half of the planula body. Scyphozoan planulae, as well as anthozoan planulae, have a sensory structure at the anterior pole called an apical organ, which is believed to take part in metamorphosis induction. Hydrozoan planulae also possess sensory cells. It has been previously shown in several cnidarian larvae that their neuronal cells contain the neurotransmitter, serotonin. The present study describes the peculiarities of serotonin-like immunoreactive cells in Aurelia aurita (Scyphozoa) and Gonothyraea loveni (Hydrozoa) planulae. We show that several cells in the presumptive apical organ of A. aurita are immunoreactive to antibodies against serotonin, while G. loveni planulae have an accumulation of serotonin-positive cells near the anterior pole. Additional serotonin-like immunoreactive cells are found in the lateral ectoderm of both planulae. Treatment of A. aurita and G. loveni planulae with serotonin or its blockers show that serotonin is likely involved in the initiation of planula settlement.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12024" xmlns="http://purl.org/rss/1.0/"><title>Humerus development in moles (Talpidae, Mammalia)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12024</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Humerus development in moles (Talpidae, Mammalia)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Constanze Bickelmann, Rafael Jiménez, Michael K. Richardson, Marcelo R. Sánchez-Villagra</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-07T06:43:31.217757-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12024</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12024</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12024</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The humerus of fossorial moles has a highly derived anatomy, reflecting the ecological specialization of these animals for digging. It is short and broad, with enlarged muscle attachment sites and pronounced articulations compared to non-fossorial sister taxa and other mammals. Both condyles are rotated in opposite directions, resulting in a torsion which is unique among eutherian mammals. The development of this exceptional bone was studied in embryonic stages of the fossorial Iberian mole (<em>Talpa occidentalis</em>) from mesenchymal condensation to incipient ossification based on histological serial sections using 3D reconstruction methods. For comparison, embryonic stages of the semi-fossorial Japanese shrew mole (<em>Urotrichus talpoides</em>) as well as a sister taxon of moles, the terrestrial North American least shrew (<em>Cryptotis parva</em>), were studied. Results show that the humerus of <em>Talpa</em> already shows its derived anatomy with broadened muscle attachment sites and distinct articulations at early cartilaginous stages, when ossification has just started in the mid-diaphyseal region. The torsion takes place simultaneously with the medial rotation of the forelimbs. The supracondylar foramen is closed in all studied <em>Talpa</em> embryos, but patent in <em>Cryptotis</em> and <em>Urotrichus</em>. This is an example of developmental penetrance, suggesting that variation of adult elements can be found at early stages as well.</p></div>
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The humerus of fossorial moles has a highly derived anatomy, reflecting the ecological specialization of these animals for digging. It is short and broad, with enlarged muscle attachment sites and pronounced articulations compared to non-fossorial sister taxa and other mammals. Both condyles are rotated in opposite directions, resulting in a torsion which is unique among eutherian mammals. The development of this exceptional bone was studied in embryonic stages of the fossorial Iberian mole (Talpa occidentalis) from mesenchymal condensation to incipient ossification based on histological serial sections using 3D reconstruction methods. For comparison, embryonic stages of the semi-fossorial Japanese shrew mole (Urotrichus talpoides) as well as a sister taxon of moles, the terrestrial North American least shrew (Cryptotis parva), were studied. Results show that the humerus of Talpa already shows its derived anatomy with broadened muscle attachment sites and distinct articulations at early cartilaginous stages, when ossification has just started in the mid-diaphyseal region. The torsion takes place simultaneously with the medial rotation of the forelimbs. The supracondylar foramen is closed in all studied Talpa embryos, but patent in Cryptotis and Urotrichus. This is an example of developmental penetrance, suggesting that variation of adult elements can be found at early stages as well.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12016" xmlns="http://purl.org/rss/1.0/"><title>Morphological characteristics of the Pterodoras granulosus digestive tube (Valenciennes, 1821) (Osteichthyes, Doradidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12016</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Morphological characteristics of the Pterodoras granulosus digestive tube (Valenciennes, 1821) (Osteichthyes, Doradidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ricardo Melo Germano, Sandra Regina Stabille, Renata Britto Mari, Joice Naiara Bertaglia Pereira, Juliana Raquel Scoz Faglioni, Marcílio Hubner Miranda Neto</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-03T23:39:50.92733-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12016</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12016</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12016</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Little is known about the digestive tube (DT) morphology of the fish <em>Pterodoras granulosus</em>. Therefore, macro-, meso- and microscopic aspects of 15 <em>P. granulosus </em>DTs were analysed. The muscular layer was composed of striated skeletal muscle in the oesophagus and smooth muscle in the other segments. The epithelium progressed from a stratified pavement in the oesophagus to a simple column in the other segments, with a flat striated border in the intestine. A large number of mucus-secreting periodic acid-Schiff (PAS)-positive cells were observed in the oesophagus. In the stomach, the number of glands in the region decreased towards the cardiac–fundic region, and none were found in the pylorus. The intestine showed an epithelium with absorption cells and an increasing number of PAS-positive caliciform cells towards the distal region. Tests showed that the oesophagus is adapted for passing and preparing food for the chemical digestion that occurs in the stomach, which also has storage functions without grinding action. The proximal intestinal region was consistent with fat absorption, and the medium region, with the absorption of other nutrients. The distal region was short and consistent with a role in absorption for osmoregulation as well as in the formation, storage and disposal of faeces.</p></div>
]]></content:encoded><description>

Little is known about the digestive tube (DT) morphology of the fish Pterodoras granulosus. Therefore, macro-, meso- and microscopic aspects of 15 P. granulosus DTs were analysed. The muscular layer was composed of striated skeletal muscle in the oesophagus and smooth muscle in the other segments. The epithelium progressed from a stratified pavement in the oesophagus to a simple column in the other segments, with a flat striated border in the intestine. A large number of mucus-secreting periodic acid-Schiff (PAS)-positive cells were observed in the oesophagus. In the stomach, the number of glands in the region decreased towards the cardiac–fundic region, and none were found in the pylorus. The intestine showed an epithelium with absorption cells and an increasing number of PAS-positive caliciform cells towards the distal region. Tests showed that the oesophagus is adapted for passing and preparing food for the chemical digestion that occurs in the stomach, which also has storage functions without grinding action. The proximal intestinal region was consistent with fat absorption, and the medium region, with the absorption of other nutrients. The distal region was short and consistent with a role in absorption for osmoregulation as well as in the formation, storage and disposal of faeces.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12015" xmlns="http://purl.org/rss/1.0/"><title>Cephalodiscus reproductive biology (Pterobranchia, Hemichordata)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12015</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cephalodiscus reproductive biology (Pterobranchia, Hemichordata)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter N. Dilly</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-16T05:27:12.948006-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12015</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12015</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12015</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Sexually mature adults and embryos and larvae of <em>Cephalodiscus nigrescens</em> and <em>C</em>. <em>gracilis</em> were studied by light and electron microscopy. Contrary to claims in the literature, individual coenecial cavities are inhabited by colonies of up to 15 joined zooids and not by single individuals, which is important for the interpretation of the mode of life of the related fossil group the graptolites. Some aspects of the reproductive apparatus and reproduction in <em>Cephalodiscus</em> are reported. The ultrastructure of the spermatozoon is described for the first time. Coelom formation is by schizocoely. The structure of the larva at several developmental stages is illustrated. Not all fertilised eggs are destined to become motile larvae and some develop into zooids omitting the motile stage. The lumen of the oviduct is much larger than previously supposed. Spermatozoa are shed into the cavity of the coenecium. It is proposed that fertilisation takes place within the coenecium. The ultrastructure of the enigmatic black ‘Comma Body’ is described and a reproductive function is proposed. Budding takes place from a base common to several zooids. This base probably also serves as an attachment foot. Large masses of yolk have been discovered within the coelom of some zooids and muscle stalks. It is inconceivable that a colony of <em>Cephalodiscus nigrescens</em> could survive unless it spent most of its life outside the coenecium.</p></div>
]]></content:encoded><description>

Sexually mature adults and embryos and larvae of Cephalodiscus nigrescens and C. gracilis were studied by light and electron microscopy. Contrary to claims in the literature, individual coenecial cavities are inhabited by colonies of up to 15 joined zooids and not by single individuals, which is important for the interpretation of the mode of life of the related fossil group the graptolites. Some aspects of the reproductive apparatus and reproduction in Cephalodiscus are reported. The ultrastructure of the spermatozoon is described for the first time. Coelom formation is by schizocoely. The structure of the larva at several developmental stages is illustrated. Not all fertilised eggs are destined to become motile larvae and some develop into zooids omitting the motile stage. The lumen of the oviduct is much larger than previously supposed. Spermatozoa are shed into the cavity of the coenecium. It is proposed that fertilisation takes place within the coenecium. The ultrastructure of the enigmatic black ‘Comma Body’ is described and a reproductive function is proposed. Budding takes place from a base common to several zooids. This base probably also serves as an attachment foot. Large masses of yolk have been discovered within the coelom of some zooids and muscle stalks. It is inconceivable that a colony of Cephalodiscus nigrescens could survive unless it spent most of its life outside the coenecium.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12022" xmlns="http://purl.org/rss/1.0/"><title>Morphology of the carpal region in some rodents with special emphasis on hystricognaths</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12022</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Morphology of the carpal region in some rodents with special emphasis on hystricognaths</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jan Prochel, Sabine Begall, Hynek Burda</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-07T21:25:29.196421-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12022</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12022</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12022</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We examined the morphology of the wrist (carpal region) skeleton using histological serial sections and cleared and stained forelimbs of representatives of three rodent clades: ‘Hystricomorpha’ (Caviomorpha: <em>Ctenomys opimus</em>,<em> C. talarum</em>,<em> Cuniculus taczanowskii</em>,<em> Erethizon dorsatum</em>,<em> Galea</em> sp., <em>Lagostomus maximus</em>,<em> Spalacopus cyanus</em>; Phiomorpha: <em>Fukomys mechowii</em>,<em> Heliophobius argenteocinereus, Hystrix cristata, H. africaeaustralis</em>; Ctenodactylids (<em>Ctenodactylus gundi</em>)), ‘Myomorpha’ (<em>Arvicola amphibius</em>,<em> Ondatra zibethicus</em>,<em> Meriones unguiculatus</em>,<em> Myodes glareolus</em>,<em> Spalax</em> sp.) and ‘Sciuromorpha’ (<em>Eliomys quercinus</em>,<em> Glis glis</em>,<em> Marmota marmota</em>). We describe the arrangement of the carpal bones and identify several variable traits, some of which represent convergent evolution. One element, the Os posthamatum, lies in the carpal region and has not been recorded before. We interpret this bone as a putative autapomorphy of Hystricognathi but not of ‘Hystricomorpha’.</p></div>
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We examined the morphology of the wrist (carpal region) skeleton using histological serial sections and cleared and stained forelimbs of representatives of three rodent clades: ‘Hystricomorpha’ (Caviomorpha: Ctenomys opimus, C. talarum, Cuniculus taczanowskii, Erethizon dorsatum, Galea sp., Lagostomus maximus, Spalacopus cyanus; Phiomorpha: Fukomys mechowii, Heliophobius argenteocinereus, Hystrix cristata, H. africaeaustralis; Ctenodactylids (Ctenodactylus gundi)), ‘Myomorpha’ (Arvicola amphibius, Ondatra zibethicus, Meriones unguiculatus, Myodes glareolus, Spalax sp.) and ‘Sciuromorpha’ (Eliomys quercinus, Glis glis, Marmota marmota). We describe the arrangement of the carpal bones and identify several variable traits, some of which represent convergent evolution. One element, the Os posthamatum, lies in the carpal region and has not been recorded before. We interpret this bone as a putative autapomorphy of Hystricognathi but not of ‘Hystricomorpha’.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12007" xmlns="http://purl.org/rss/1.0/"><title>Skeletogenesis in anurans: cranial and postcranial development in metamorphic and postmetamorphic stages of Leptodactylus bufonius (Anura: Leptodactylidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12007</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Skeletogenesis in anurans: cranial and postcranial development in metamorphic and postmetamorphic stages of Leptodactylus bufonius (Anura: Leptodactylidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Miriam Corina Vera, María Laura Ponssa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-07T07:16:35.427164-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12007</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12007</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12007</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Osteological studies of anurans generally have focused on the descriptions of adults and larval chondrocrania, including developmental series of chondrocrania. Thus, the changes occurring during postmetamorphic stages have largely been overlooked. Herein, we describe cranial and postcranial skeletogenesis, and change in skull shape through the metamorphic and postmetamorphic development of <em>Leptodactylus bufonius</em>. Several elements, particularly those of the cranium, are already ossified at metamorphic climax; among these elements are the frontoparietals, prootics, premaxillae, maxillae, squamosals, pterygoids, neopalatines, angulosplenials, dentaries, mentomeckelians, and the mesosternum. Determining the exact timing of ossification of some elements is difficult because variation in their development may result from extrinsic factors. The otic region and that of the jaw closure undergo the greatest changes in shape, which may imply functional constraints. The development of many skeletal elements is still incomplete at metamorphosis; thus, the changes occurring postmetamorphically are crucial to achieving the configuration and function of an adult skeleton. María Laura Ponssa. CONICET. Instituto de Herpetología, Fundación Miguel Lillo. S. M. de Tucumán, c/p (4000), Argentina. E-mail: <!--TODO: clickthrough URL--><a href="mailto:mlponssa@hotmail.com" title="Link to email address">mlponssa@hotmail.com</a>.</p></div>
]]></content:encoded><description>

Osteological studies of anurans generally have focused on the descriptions of adults and larval chondrocrania, including developmental series of chondrocrania. Thus, the changes occurring during postmetamorphic stages have largely been overlooked. Herein, we describe cranial and postcranial skeletogenesis, and change in skull shape through the metamorphic and postmetamorphic development of Leptodactylus bufonius. Several elements, particularly those of the cranium, are already ossified at metamorphic climax; among these elements are the frontoparietals, prootics, premaxillae, maxillae, squamosals, pterygoids, neopalatines, angulosplenials, dentaries, mentomeckelians, and the mesosternum. Determining the exact timing of ossification of some elements is difficult because variation in their development may result from extrinsic factors. The otic region and that of the jaw closure undergo the greatest changes in shape, which may imply functional constraints. The development of many skeletal elements is still incomplete at metamorphosis; thus, the changes occurring postmetamorphically are crucial to achieving the configuration and function of an adult skeleton. María Laura Ponssa. CONICET. Instituto de Herpetología, Fundación Miguel Lillo. S. M. de Tucumán, c/p (4000), Argentina. E-mail: mlponssa@hotmail.com.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12021" xmlns="http://purl.org/rss/1.0/"><title>Sexual dimorphism in histological characteristics and contractility of the iliofibularis muscle in the lizard Sceloporus torquatus</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12021</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sexual dimorphism in histological characteristics and contractility of the iliofibularis muscle in the lizard Sceloporus torquatus</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Erendira Quintana, Javier Manjarrez, Margarita Martínez-Gómez, Liliana D'Alba, Jorge Rodríguez-Antolín, Victor Fajardo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-28T02:01:19.257592-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12021</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12021</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12021</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The iliofibularis is a hindlimb muscle used in lizard locomotion that is composed of at least three types of fibres: fast-twitch-glycolytic (FG), fast-twitch-oxidative-glycolytic fibre (FOG) and slow-twitch-oxidative (SO). The striated skeletal muscle is a highly plastic tissue undergoing phenotypic change in response to activity. The lizard <em>Sceloporus torquatus</em> has sexual differences associated with microhabitat use, which can be reflected in the physiology and anatomy of the muscle, and thus, in our study, we analysed the morphological and contractile characteristics of the iliofibularis muscle (IF) of <em>S. torquatus</em> males and females. We found a larger prevalence of FOG compared with FG and SO fibres in the muscle of both sexes. We also found that males show larger areas of the three types of fibres, develop greater strength but also faster fatigue than females, suggesting that strength is a key functional feature that enables males to perform faster movements (but for shorter periods), associated with the demands of territoriality.</p></div>
]]></content:encoded><description>

The iliofibularis is a hindlimb muscle used in lizard locomotion that is composed of at least three types of fibres: fast-twitch-glycolytic (FG), fast-twitch-oxidative-glycolytic fibre (FOG) and slow-twitch-oxidative (SO). The striated skeletal muscle is a highly plastic tissue undergoing phenotypic change in response to activity. The lizard Sceloporus torquatus has sexual differences associated with microhabitat use, which can be reflected in the physiology and anatomy of the muscle, and thus, in our study, we analysed the morphological and contractile characteristics of the iliofibularis muscle (IF) of S. torquatus males and females. We found a larger prevalence of FOG compared with FG and SO fibres in the muscle of both sexes. We also found that males show larger areas of the three types of fibres, develop greater strength but also faster fatigue than females, suggesting that strength is a key functional feature that enables males to perform faster movements (but for shorter periods), associated with the demands of territoriality.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12018" xmlns="http://purl.org/rss/1.0/"><title>A morphological, morphometric and histochemical study of the oviduct in pregnant and non-pregnant females of the plains viscacha (Lagostomus maximus)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12018</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A morphological, morphometric and histochemical study of the oviduct in pregnant and non-pregnant females of the plains viscacha (Lagostomus maximus)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mirta A. Flamini, Claudio G. Barbeito, Enrique L. Portiansky</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-28T02:01:15.976753-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12018</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12018</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12018</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The oviduct is a very thin organ with a very tortuous appearance. It is divided into three segments: the infundibulum, the ampulla and the isthmus. Particularly, the oviduct of the viscacha lacks the intramural portion described in other species. The mucosa shows longitudinal pleats. The free edge of the infundibulum ends as small fimbriae that are of variable length and do not completely cover the ovary. The proportion of ciliated and secretory epithelial cells varied both in relation to the segments of the oviduct analysed and to the physiological state (anoestrus, follicular phase, early pregnancy and late pregnancy). The glycocalix and the apical region of the superficial epithelial cells are PAS and alcian-blue positive. The muscular layers vary in thickness in different regions. Some lectins such as UEA-1 and DBA showed variations in the binding pattern during the different physiological stages analysed whereas RCA-1and WGA had a very stable pattern.</p></div>
]]></content:encoded><description>

The oviduct is a very thin organ with a very tortuous appearance. It is divided into three segments: the infundibulum, the ampulla and the isthmus. Particularly, the oviduct of the viscacha lacks the intramural portion described in other species. The mucosa shows longitudinal pleats. The free edge of the infundibulum ends as small fimbriae that are of variable length and do not completely cover the ovary. The proportion of ciliated and secretory epithelial cells varied both in relation to the segments of the oviduct analysed and to the physiological state (anoestrus, follicular phase, early pregnancy and late pregnancy). The glycocalix and the apical region of the superficial epithelial cells are PAS and alcian-blue positive. The muscular layers vary in thickness in different regions. Some lectins such as UEA-1 and DBA showed variations in the binding pattern during the different physiological stages analysed whereas RCA-1and WGA had a very stable pattern.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12019" xmlns="http://purl.org/rss/1.0/"><title>Periostracal mineralization in the gastrochaenid bivalve Spengleria</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12019</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Periostracal mineralization in the gastrochaenid bivalve Spengleria</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Antonio G. Checa, Elizabeth M. Harper</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-20T03:52:24.270621-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12019</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12019</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12019</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We investigated the spikes on the outer shell surface of the endolithic gastrochaenid bivalve genus <em>Spengleria</em> with a view to understand the mechanism by which they form and evaluate their homology with spikes in other heterodont and palaeoheterodont bivalves. We discovered that spike formation varied in mechanism between different parts of the valve. In the posterior region, spikes form within the translucent layer of the periostracum but separated from the calcareous part of the shell. By contrast those spikes in the anterior and ventral region, despite also forming within the translucent periostracal layer, become incorporated into the outer shell layer. Spikes in the posterior area of <em>Spengleria mytiloides</em> form only on the outer surface of the periostracum and are therefore, not encased in periostracal material. Despite differences in construction between these gastrochaenid spikes and those of other heterodont and palaeoheterodont bivalves, all involve calcification of the inner translucent periostracal layer which may indicate a deeper homology.</p></div>
]]></content:encoded><description>

We investigated the spikes on the outer shell surface of the endolithic gastrochaenid bivalve genus Spengleria with a view to understand the mechanism by which they form and evaluate their homology with spikes in other heterodont and palaeoheterodont bivalves. We discovered that spike formation varied in mechanism between different parts of the valve. In the posterior region, spikes form within the translucent layer of the periostracum but separated from the calcareous part of the shell. By contrast those spikes in the anterior and ventral region, despite also forming within the translucent periostracal layer, become incorporated into the outer shell layer. Spikes in the posterior area of Spengleria mytiloides form only on the outer surface of the periostracum and are therefore, not encased in periostracal material. Despite differences in construction between these gastrochaenid spikes and those of other heterodont and palaeoheterodont bivalves, all involve calcification of the inner translucent periostracal layer which may indicate a deeper homology.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12020" xmlns="http://purl.org/rss/1.0/"><title>Tyrosine phosphatase inhibitor triggers rodlet cell discharge in sunfish scale epidermis cultures</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12020</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Tyrosine phosphatase inhibitor triggers rodlet cell discharge in sunfish scale epidermis cultures</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joseph A. DePasquale</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-20T03:46:17.534852-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12020</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12020</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12020</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Epidermal rodlet cells were evaluated after treatment with the tyrosine phosphatase inhibitor pervanadate. Treatment of sunfish explant cell cultures with the inhibitor triggered a contraction of the rodlet cells and expulsion of cell contents. Time-lapse video differential interference contrast (DIC) microscopy was used to evaluate rodlet cell contraction and rodlet discharge. Three general steps in pervanadate triggered discharge were identified. First the rodlet cell undergoes a constriction of the midsection. Constriction is followed by a rapid forward movement of rodlets and sacs to the apical end of cell, culminating in discharge of rodlets and other cellular contents, including the nucleus. A ring-shaped structure around the apical pore was identified with DIC microscopy. Fluorescent-labeled phalloidin and antibodies to alpha-actinin and phosphotyrosine strongly stained the apical ring. A diffuse granular staining for both antibodies was also observed throughout the fibrous capsule. The results suggest that tyrosine kinases play a role in rodlet cell contraction. Alpha-actinin is a known substrate for tyrosine kinases and is a potential target for triggering rodlet cell contraction and rodlet ejection. Modification of alpha-actinin tyrosines could also be a mechanism for regulating the structural integrity of the fibrous capsule.</p></div>
]]></content:encoded><description>

Epidermal rodlet cells were evaluated after treatment with the tyrosine phosphatase inhibitor pervanadate. Treatment of sunfish explant cell cultures with the inhibitor triggered a contraction of the rodlet cells and expulsion of cell contents. Time-lapse video differential interference contrast (DIC) microscopy was used to evaluate rodlet cell contraction and rodlet discharge. Three general steps in pervanadate triggered discharge were identified. First the rodlet cell undergoes a constriction of the midsection. Constriction is followed by a rapid forward movement of rodlets and sacs to the apical end of cell, culminating in discharge of rodlets and other cellular contents, including the nucleus. A ring-shaped structure around the apical pore was identified with DIC microscopy. Fluorescent-labeled phalloidin and antibodies to alpha-actinin and phosphotyrosine strongly stained the apical ring. A diffuse granular staining for both antibodies was also observed throughout the fibrous capsule. The results suggest that tyrosine kinases play a role in rodlet cell contraction. Alpha-actinin is a known substrate for tyrosine kinases and is a potential target for triggering rodlet cell contraction and rodlet ejection. Modification of alpha-actinin tyrosines could also be a mechanism for regulating the structural integrity of the fibrous capsule.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12017" xmlns="http://purl.org/rss/1.0/"><title>Structure of the male reproductive system of the blue swimmer crab Portunus pelagicus (Decapoda: Portunidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12017</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Structure of the male reproductive system of the blue swimmer crab Portunus pelagicus (Decapoda: Portunidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Raghunath Ravi, Mary Kurian Manisseri, Nandiath Karayi Sanil</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-12T05:34:22.243539-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12017</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12017</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12017</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>An attempt was made here to study the structure of the male reproductive system of <em>Portunus pelagicus</em>, which would improve the knowledge base on the reproductive biology of the species and also help in the maintenance of broodstock under controlled conditions. Male <em>P. pelagicus</em> of different sizes were collected from the Palk Bay off Mandapam (9°17′ N, 79°9′ E) and maintained under controlled conditions for the study. Tissues from testis, anterior vas deferens (AVD), median vas deferens (MVD), posterior vas deferens (PVD), ejaculatory duct and penis were fixed in Bouin's fluid and 2.5% buffered glutaraldehyde separately and processed for light and electron microscopic studies, respectively. The reproductive system consisted of testis, commissure, vas deferens, ejaculatory duct and penis. The vas deferens was divided based on the morphology and/or histology into AVD, MVD and PVD. The AVD was further divided based on histology into proximal and distal regions, and the MVD, based on diameter into major and minor coils. The testicular lobe had several lobules with a central seminiferous tubule, which continued till the penis. The seminiferous tubule was lined by a layer of cuboidal or columnar epithelium. The lining of the central tubule of the vas deferens formed several ‘folds’, which at times formed ‘pouches’. High incidence of cell organelles in the columnar epithelial cells, aggregations of vesicles and occurrence of blebs at the luminal periphery and the projection of numerous microvilli containing electron-dense materials into the lumen from the cell lining denoted high secretory activity of the epithelial cells.</p></div>
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An attempt was made here to study the structure of the male reproductive system of Portunus pelagicus, which would improve the knowledge base on the reproductive biology of the species and also help in the maintenance of broodstock under controlled conditions. Male P. pelagicus of different sizes were collected from the Palk Bay off Mandapam (9°17′ N, 79°9′ E) and maintained under controlled conditions for the study. Tissues from testis, anterior vas deferens (AVD), median vas deferens (MVD), posterior vas deferens (PVD), ejaculatory duct and penis were fixed in Bouin's fluid and 2.5% buffered glutaraldehyde separately and processed for light and electron microscopic studies, respectively. The reproductive system consisted of testis, commissure, vas deferens, ejaculatory duct and penis. The vas deferens was divided based on the morphology and/or histology into AVD, MVD and PVD. The AVD was further divided based on histology into proximal and distal regions, and the MVD, based on diameter into major and minor coils. The testicular lobe had several lobules with a central seminiferous tubule, which continued till the penis. The seminiferous tubule was lined by a layer of cuboidal or columnar epithelium. The lining of the central tubule of the vas deferens formed several ‘folds’, which at times formed ‘pouches’. High incidence of cell organelles in the columnar epithelial cells, aggregations of vesicles and occurrence of blebs at the luminal periphery and the projection of numerous microvilli containing electron-dense materials into the lumen from the cell lining denoted high secretory activity of the epithelial cells.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12011" xmlns="http://purl.org/rss/1.0/"><title>Comparative morphology of the tentorium and hypopharyngeal–premental sclerites in sporophagous and non-sporophagous adult Aleocharinae (Coleoptera: Staphylinidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12011</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparative morphology of the tentorium and hypopharyngeal–premental sclerites in sporophagous and non-sporophagous adult Aleocharinae (Coleoptera: Staphylinidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Daniela Weide, Margaret K. Thayer, Oliver Betz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-10T04:45:52.060358-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12011</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12011</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12011</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We elucidate the configuration of the tentorium and the sclerites of the hypopharynx–prementum complex in selected spore- (pollen-) and non-spore-feeding Aleocharinae (Staphylinidae) by presenting the first comparative 3D reconstructions of these structures for 19 staphylinoid beetle species (six outgroups, 13 Aleocharinae). General organization of the tentorium follows the groundplan previously proposed for adult Staphylinidae, although some taxa have reduced or lost the dorsal (all Aleocharinae studied, <em>Agathidium mandibulare</em> [Leiodidae]) or anterior (<em>Omalium rivulare</em> [Omaliinae], <em>Anotylus sculpturatus</em> [Oxytelinae]) tentorial arms. All species investigated have premental and hypopharyngeal sclerites that are partly homologizable across taxa. We clarified that Musculus praementopalpalis externus originates from the premental sclerite, resolving its unclear origin reported in our previous publications. Eight of 13 investigated Aleocharinae species are spore/pollen feeders, six obligatorily. Three of these six (<em>Eumicrota</em>,<em> Gyrophaena fasciata</em>,<em> G. gentilis</em>) have grinding pseudomolae and a fully developed hypopharyngeal suspensorium with posterior bridge and anterior elongations; the remaining three (<em>Oxypoda, Pagla, Polylobus</em>) lack pseudomolae and suspensorial bridge, but have the suspensorium elongated anteriorly. The dorsolateral side of the hypopharyngeal sclerite interacts with the pseudomola. Obligate sporophagy/pollinivory apparently arose at least three times in Aleocharinae, not always involving the pseudomola–hypopharynx grinding mechanism.</p></div>
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We elucidate the configuration of the tentorium and the sclerites of the hypopharynx–prementum complex in selected spore- (pollen-) and non-spore-feeding Aleocharinae (Staphylinidae) by presenting the first comparative 3D reconstructions of these structures for 19 staphylinoid beetle species (six outgroups, 13 Aleocharinae). General organization of the tentorium follows the groundplan previously proposed for adult Staphylinidae, although some taxa have reduced or lost the dorsal (all Aleocharinae studied, Agathidium mandibulare [Leiodidae]) or anterior (Omalium rivulare [Omaliinae], Anotylus sculpturatus [Oxytelinae]) tentorial arms. All species investigated have premental and hypopharyngeal sclerites that are partly homologizable across taxa. We clarified that Musculus praementopalpalis externus originates from the premental sclerite, resolving its unclear origin reported in our previous publications. Eight of 13 investigated Aleocharinae species are spore/pollen feeders, six obligatorily. Three of these six (Eumicrota, Gyrophaena fasciata, G. gentilis) have grinding pseudomolae and a fully developed hypopharyngeal suspensorium with posterior bridge and anterior elongations; the remaining three (Oxypoda, Pagla, Polylobus) lack pseudomolae and suspensorial bridge, but have the suspensorium elongated anteriorly. The dorsolateral side of the hypopharyngeal sclerite interacts with the pseudomola. Obligate sporophagy/pollinivory apparently arose at least three times in Aleocharinae, not always involving the pseudomola–hypopharynx grinding mechanism.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12014" xmlns="http://purl.org/rss/1.0/"><title>Cranial osteology of Picini (Aves: Piciformes: Picidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12014</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cranial osteology of Picini (Aves: Piciformes: Picidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Reginaldo J. Donatelli</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-03T00:27:01.310507-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12014</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12014</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12014</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The Picini is composed of 26 species of woodpeckers from the old world that are grouped into seven genera. Given the absence of detailed studies on the cranial osteology of the Picini, the purpose of this study is to describe the cranial osteology of 14 species of Picini from six genera and to compare these species with each other, with other species of woodpeckers and with other bird groups. The results of the analysis of the bone structures of the skull of the Picini indicate that there are seven outstanding characteristic of bones involved in the functional mechanistics of the jaw apparatus. In the <em>ossa cranii</em>, these include the frontal overhang, the postorbital process, the extension of the parietal versus the frontal region and the temporal fossa. In the <em>ossa faciei</em>, these include the rostral expansion of the pterygoid, the ventral palatine fossa and the orbital process of the quadrate bone. For all of the structures associated with the cranial osteology of the investigated species, there is a clear distinction between the species of the genus <em>Picus</em> and the other species studied. <em>Blythipicus rubiginosus</em>,<em> Chrysocolaptes lucidus</em>,<em> Reinwardtipicus validus</em>,<em> Gecinulus viridis</em> and the species of the genus <em>Dinopium</em> exhibit additional particularities.</p></div>
]]></content:encoded><description>

The Picini is composed of 26 species of woodpeckers from the old world that are grouped into seven genera. Given the absence of detailed studies on the cranial osteology of the Picini, the purpose of this study is to describe the cranial osteology of 14 species of Picini from six genera and to compare these species with each other, with other species of woodpeckers and with other bird groups. The results of the analysis of the bone structures of the skull of the Picini indicate that there are seven outstanding characteristic of bones involved in the functional mechanistics of the jaw apparatus. In the ossa cranii, these include the frontal overhang, the postorbital process, the extension of the parietal versus the frontal region and the temporal fossa. In the ossa faciei, these include the rostral expansion of the pterygoid, the ventral palatine fossa and the orbital process of the quadrate bone. For all of the structures associated with the cranial osteology of the investigated species, there is a clear distinction between the species of the genus Picus and the other species studied. Blythipicus rubiginosus, Chrysocolaptes lucidus, Reinwardtipicus validus, Gecinulus viridis and the species of the genus Dinopium exhibit additional particularities.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12013" xmlns="http://purl.org/rss/1.0/"><title>Rodlet cells in epidermal explant cultures of Lepomis Macrochirus</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12013</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Rodlet cells in epidermal explant cultures of Lepomis Macrochirus</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joseph A. DePasquale</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-28T18:34:30.709318-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12013</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12013</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12013</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Sunfish rodlet cells were examined <em>in vitro</em> using a novel tissue explant system. Outgrowth of epidermal cell layers from explanted fish scales enabled both live cell videomicroscopy and immunocytochemical analysis of rodlet cells within the cell layer. Cells stained with fluorescent phallotoxin and antibody to tubulin showed that F-actin is a component of the fibrous capsule that envelopes the cell and a microtubule network extends from the basal to apical ends of the cell interior. The fibrous capsule is also enriched for phosphotyrosine suggesting a potential signal-transducing capability is present in this structure. Videomicroscopy analysis of live explant cultures demonstrated that rodlet cells are immobile and that interior structures are highly dynamic. Rodlet sacs can undergo extension and retraction, while intracellular particles can move rapidly within these cells. Fish scale tissue explants provide a useful system for analyzing the molecular composition and dynamic behavior of rodlet cells.</p></div>
]]></content:encoded><description>

Sunfish rodlet cells were examined in vitro using a novel tissue explant system. Outgrowth of epidermal cell layers from explanted fish scales enabled both live cell videomicroscopy and immunocytochemical analysis of rodlet cells within the cell layer. Cells stained with fluorescent phallotoxin and antibody to tubulin showed that F-actin is a component of the fibrous capsule that envelopes the cell and a microtubule network extends from the basal to apical ends of the cell interior. The fibrous capsule is also enriched for phosphotyrosine suggesting a potential signal-transducing capability is present in this structure. Videomicroscopy analysis of live explant cultures demonstrated that rodlet cells are immobile and that interior structures are highly dynamic. Rodlet sacs can undergo extension and retraction, while intracellular particles can move rapidly within these cells. Fish scale tissue explants provide a useful system for analyzing the molecular composition and dynamic behavior of rodlet cells.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12008" xmlns="http://purl.org/rss/1.0/"><title>Structural organization of the toe pads in the amphibian Philautus annandalii (Boulenger, 1906)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12008</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Structural organization of the toe pads in the amphibian Philautus annandalii (Boulenger, 1906)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Saurabh Chakraborti, Debasish Das, Subrata K. De, Tapas C. Nag</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T04:51:21.1956-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12008</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12008</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12008</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We describe the morphology of toe pads in the Himalayan tree frog <em>Philautus annandalii</em>. These are expanded tips of digits and show modifications of their ventral epidermis for adhesion. The outer cells of toe pad epidermis (TPE) bear surface microstructures (0.7 × 0.2 μm), which are keratinized. Their cytoplasm contains no organelles, but pleomorphic nuclei and mucous granules (0.4–0.5 μm) that glue the keratin filaments. In the intermediate cell layer of TPE, similar keratinized microstructures as in the outer cells are present, so that when the outer layer is shed, it is ready with features for adhesion. These cells contain more keratin than the outer cells. The basal cell layer contains thin keratin bundles and usual cell organelles. The dermis contains mucous-secreting glands, whose ducts open in the outer epidermal cell layer in channels. The dorsal epidermal cells lack surface microstructures and keratin bundles. Ultrastructural features suggest that toe pads utilize the surface microstructures for adhesion aided by mucus, in which the intermediate cell layer seems to bear the shear stress generated during locomotion. Further, TPE can expand and fit into an increased contact area of the substrate. The long, surface microstructures may also help in mechanical interlocking with rough surfaces on plants.</p></div>
]]></content:encoded><description>

We describe the morphology of toe pads in the Himalayan tree frog Philautus annandalii. These are expanded tips of digits and show modifications of their ventral epidermis for adhesion. The outer cells of toe pad epidermis (TPE) bear surface microstructures (0.7 × 0.2 μm), which are keratinized. Their cytoplasm contains no organelles, but pleomorphic nuclei and mucous granules (0.4–0.5 μm) that glue the keratin filaments. In the intermediate cell layer of TPE, similar keratinized microstructures as in the outer cells are present, so that when the outer layer is shed, it is ready with features for adhesion. These cells contain more keratin than the outer cells. The basal cell layer contains thin keratin bundles and usual cell organelles. The dermis contains mucous-secreting glands, whose ducts open in the outer epidermal cell layer in channels. The dorsal epidermal cells lack surface microstructures and keratin bundles. Ultrastructural features suggest that toe pads utilize the surface microstructures for adhesion aided by mucus, in which the intermediate cell layer seems to bear the shear stress generated during locomotion. Further, TPE can expand and fit into an increased contact area of the substrate. The long, surface microstructures may also help in mechanical interlocking with rough surfaces on plants.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12012" xmlns="http://purl.org/rss/1.0/"><title>Sexual size dimorphism in greater mouse-eared bat Myotis myotis (Chiroptera: Vespertilionidae) from a Mediterranean region</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12012</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sexual size dimorphism in greater mouse-eared bat Myotis myotis (Chiroptera: Vespertilionidae) from a Mediterranean region</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fulgencio Lisón, Ángeles Haz, Carlos González-Revelles, José F. Calvo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T04:43:33.920413-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12012</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12012</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12012</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Although sexual size dimorphism (SSD) is common among mammals, there is no clear explanation for its maintenance in nature. Bats are one of the few groups of mammals where reverse SSD appears. In this group, the size of individuals may have very important ecological consequences related with flight. In this study, we examine sexual dimorphism in the wing measurements of 195 adult individuals (141 males and 54 females) of the greater mouse-eared bat <em>Myotis myotis</em> in the south-east of the Iberian Peninsula. We also investigated size differences between paired and single males in a swarming roost. The results indicate that there are significant differences in the wing measurements between sexes, females being bigger than males in this respect. While no significant differences in the wing measurements of paired and single males were observed, significant differences were found in their relative weight and fitness, single males being significantly heavier and having a better physical condition. We discuss the implications of SSD for the female of <em>M. myotis</em> in terms of reproductive advantages, trophic niche segregation and a greater ability to move, which may favour gene flow between populations.</p></div>
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Although sexual size dimorphism (SSD) is common among mammals, there is no clear explanation for its maintenance in nature. Bats are one of the few groups of mammals where reverse SSD appears. In this group, the size of individuals may have very important ecological consequences related with flight. In this study, we examine sexual dimorphism in the wing measurements of 195 adult individuals (141 males and 54 females) of the greater mouse-eared bat Myotis myotis in the south-east of the Iberian Peninsula. We also investigated size differences between paired and single males in a swarming roost. The results indicate that there are significant differences in the wing measurements between sexes, females being bigger than males in this respect. While no significant differences in the wing measurements of paired and single males were observed, significant differences were found in their relative weight and fitness, single males being significantly heavier and having a better physical condition. We discuss the implications of SSD for the female of M. myotis in terms of reproductive advantages, trophic niche segregation and a greater ability to move, which may favour gene flow between populations.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12010" xmlns="http://purl.org/rss/1.0/"><title>Ultrastructure and distribution of sensilla on the antennae of female fig wasp Eupristina sp. (Hymenoptera: Agaonidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12010</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ultrastructure and distribution of sensilla on the antennae of female fig wasp Eupristina sp. (Hymenoptera: Agaonidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zongbo Li, Pei Yang, Yanqiong Peng, Darong Yang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-23T00:19:05.849018-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12010</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12010</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12010</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In the species-specific and obligate mutualism between the fig (Moraceae: <em>Ficus</em> spp.) and its pollinator (Hymenoptera: Agaonidae), the continuity of lifecycle of both partners completely depends on the female pollinator's ability to detect receptive figs. To better understand the chemical location mechanism, we examined the antennae and their sensilla of the female fig pollinator <em>Eupristina</em> sp. using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The antennae of female <em>Eupristina</em> sp. are geniculated, and in total, there were seven types of sensilla found on the antennae: two types of multiporous placoid sensilla (type 1 is sausage-like and type 2 is rounded), sensilla trichodea (ST), basiconic sensilla (BS), chaetica sensilla (ChS), coeloconic sensilla (CoS), and one specialized sensillum classified as sensillum obscurum (SO). We described external morphology, abundance, distribution, ultrastructure and discussed putative functions. We inferred from their ultrastructures as chemoreceptors that two types of multiporous placoid sensilla, BS and CoS, were innervated by sensory neurons. The aporous type ST, ChS, and SO were not innervated by dendrites which may function as mechanoreceptor/proprioceptor. These results were also discussed in relation to the interaction between <em>Eupristina</em> sp. and its host fig.</p></div>
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In the species-specific and obligate mutualism between the fig (Moraceae: Ficus spp.) and its pollinator (Hymenoptera: Agaonidae), the continuity of lifecycle of both partners completely depends on the female pollinator's ability to detect receptive figs. To better understand the chemical location mechanism, we examined the antennae and their sensilla of the female fig pollinator Eupristina sp. using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The antennae of female Eupristina sp. are geniculated, and in total, there were seven types of sensilla found on the antennae: two types of multiporous placoid sensilla (type 1 is sausage-like and type 2 is rounded), sensilla trichodea (ST), basiconic sensilla (BS), chaetica sensilla (ChS), coeloconic sensilla (CoS), and one specialized sensillum classified as sensillum obscurum (SO). We described external morphology, abundance, distribution, ultrastructure and discussed putative functions. We inferred from their ultrastructures as chemoreceptors that two types of multiporous placoid sensilla, BS and CoS, were innervated by sensory neurons. The aporous type ST, ChS, and SO were not innervated by dendrites which may function as mechanoreceptor/proprioceptor. These results were also discussed in relation to the interaction between Eupristina sp. and its host fig.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12009" xmlns="http://purl.org/rss/1.0/"><title>Seromucous anal gland in a New World hystricognath rodent Thrichomys apereoides (Lund, 1839)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12009</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Seromucous anal gland in a New World hystricognath rodent Thrichomys apereoides (Lund, 1839)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sônia A. Talamoni, Miguel Angelo C. Assis, Melina Maciel F. Freitas, Hugo Pereira Godinho, Nilo Bazzoli</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-19T07:21:00.796784-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12009</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12009</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12009</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>New World species of the Hystricognathi comprise a group of rodents that exhibit poorly understood social behaviour. One such species, the echimyid <em>Thrichomys apereoides</em>, has a behavioural and social repertoire which suggests the use of its eversible anal gland in communication between individuals; however, no information on the morphology of this gland is available. In this study, the anal gland of nineteen adult individuals (11 males and 8 females) was analysed through histological and histochemical techniques. The gland was located in the submucosal of the anal region, cranial to the anus, and had an opening located dorsally in the rectum mucosa at approximately 1 mm from the anus. The gland was characterized as seromucous, secreting neutral glycoprotein. Not all individuals studied presented secretion in the glandular ducts, indicating a possible functional variation in the gland. This was the first record of an anal gland of the seromucous type in rodents.</p></div>
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New World species of the Hystricognathi comprise a group of rodents that exhibit poorly understood social behaviour. One such species, the echimyid Thrichomys apereoides, has a behavioural and social repertoire which suggests the use of its eversible anal gland in communication between individuals; however, no information on the morphology of this gland is available. In this study, the anal gland of nineteen adult individuals (11 males and 8 females) was analysed through histological and histochemical techniques. The gland was located in the submucosal of the anal region, cranial to the anus, and had an opening located dorsally in the rectum mucosa at approximately 1 mm from the anus. The gland was characterized as seromucous, secreting neutral glycoprotein. Not all individuals studied presented secretion in the glandular ducts, indicating a possible functional variation in the gland. This was the first record of an anal gland of the seromucous type in rodents.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12005" xmlns="http://purl.org/rss/1.0/"><title>Comparative ultrastructure of the spermatozoa of the Majoidea (Crustacea, Decapoda, Brachyura) with new data on six species in five genera</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12005</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparative ultrastructure of the spermatozoa of the Majoidea (Crustacea, Decapoda, Brachyura) with new data on six species in five genera</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christopher C. Tudge,  David M. Scheltinga,  Barrie G. M. Jamieson,  Danièle Guinot, Bertrand Richer de Forges</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-07T01:10:01.720345-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12005</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12005</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12005</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Comparative ultrastructure of majoid spermatozoa belonging to 23 species, in 19 genera and five families, is considered, with new data on <em>Schizophrys aspera</em>;<em> S. rufescens</em> (Majidae, Majinae); <em>Camposcia retusa</em> (Inachidae); <em>Pyromaia tuberculata</em> (Inachoididae); and <em>Huenia heraldica</em> and <em>Menaethius monoceros</em> (Epialtidae, Epialtinae). The oregoniid <em>Chionoecetes opilio</em>, and inachids <em>Cyrtomaia furici</em>,<em> Platymaia rebierei</em>,<em> Macropodia longirostris</em> and <em>Inachus phalangium</em>, possibly with <em>Camposcia retusa</em>, but not <em>Podochela riisei</em>, appear to form a group. Within the inachids, <em>Macropodia</em> and <em>Inachus</em> are especially close. A domed central acrosome zone, seen in most inachid sperm, in majines (both <em>Schizophrys</em> species), in pisines (<em>Oxypleurodon orbiculatus</em> and <em>O. stuckiae</em>) and epialtines (<em>Huenia heraldica</em> and <em>Menaethius monoceros</em>), appears to be an autapomorphy of these majoids. A peripheral acrosome zone is seen in the inachid <em>Grypacheus hyalinus</em>, two inachoidids (<em>P. tuberculata</em> and <em>Stenorhynchus seticornis</em>) and the majid <em>Maja squinado</em>. <em>Pyromaia tuberculata</em> differs from other inachoidids in having a slightly dome-shaped operculum. The mithracine <em>Macrocoeloma trispinosum</em> (Majidae) sperm more closely resembles Inachoididae, than Inachidae. Spermatologically, the family Majidae and the subfamily Majinae are not homogeneous. Spermatozoal ultrastructure does not support a majoid–hymenosomatid relationship and is equivocal with regard to the placement of Cryptochiridae in either the Thoracotremata or Heterotremata, the prominent operculum strongly differentiates cryptochirids from Majoidea.</p></div>
]]></content:encoded><description>

Comparative ultrastructure of majoid spermatozoa belonging to 23 species, in 19 genera and five families, is considered, with new data on Schizophrys aspera; S. rufescens (Majidae, Majinae); Camposcia retusa (Inachidae); Pyromaia tuberculata (Inachoididae); and Huenia heraldica and Menaethius monoceros (Epialtidae, Epialtinae). The oregoniid Chionoecetes opilio, and inachids Cyrtomaia furici, Platymaia rebierei, Macropodia longirostris and Inachus phalangium, possibly with Camposcia retusa, but not Podochela riisei, appear to form a group. Within the inachids, Macropodia and Inachus are especially close. A domed central acrosome zone, seen in most inachid sperm, in majines (both Schizophrys species), in pisines (Oxypleurodon orbiculatus and O. stuckiae) and epialtines (Huenia heraldica and Menaethius monoceros), appears to be an autapomorphy of these majoids. A peripheral acrosome zone is seen in the inachid Grypacheus hyalinus, two inachoidids (P. tuberculata and Stenorhynchus seticornis) and the majid Maja squinado. Pyromaia tuberculata differs from other inachoidids in having a slightly dome-shaped operculum. The mithracine Macrocoeloma trispinosum (Majidae) sperm more closely resembles Inachoididae, than Inachidae. Spermatologically, the family Majidae and the subfamily Majinae are not homogeneous. Spermatozoal ultrastructure does not support a majoid–hymenosomatid relationship and is equivocal with regard to the placement of Cryptochiridae in either the Thoracotremata or Heterotremata, the prominent operculum strongly differentiates cryptochirids from Majoidea.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12006" xmlns="http://purl.org/rss/1.0/"><title>Character distribution maps: a visualization method for comparative cladistics</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12006</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Character distribution maps: a visualization method for comparative cladistics</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">John A. Whitlock, Jeffrey A. Wilson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-02T04:36:09.709897-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12006</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12006</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12006</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The rise of computational methods and widespread availability of phylogenetic software packages has resulted in a dramatic increase in the number of phylogenetic analyses published each year. We anticipate that as the number of workers and the number of analyses continues to increase, interest in so-called ‘meta-analyses’ that compare not just the resultant trees, but the data themselves, will also increase. Here, we demonstrate a simple method for authors to facilitate such comparisons by visually representing the character data included in their analyses, the Character Distribution Map (CDM).</p></div>
]]></content:encoded><description>

The rise of computational methods and widespread availability of phylogenetic software packages has resulted in a dramatic increase in the number of phylogenetic analyses published each year. We anticipate that as the number of workers and the number of analyses continues to increase, interest in so-called ‘meta-analyses’ that compare not just the resultant trees, but the data themselves, will also increase. Here, we demonstrate a simple method for authors to facilitate such comparisons by visually representing the character data included in their analyses, the Character Distribution Map (CDM).
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12004" xmlns="http://purl.org/rss/1.0/"><title>Histology of the venom gland of Trachinus draco (Actinopterygii, Trachinidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12004</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Histology of the venom gland of Trachinus draco (Actinopterygii, Trachinidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrés Portillo Strempel, Enrique Herrera Ceballos</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-01T04:11:07.722928-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12004</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12004</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12004</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The structure of the venom gland of <em>Trachinus draco</em> was studied by histological techniques using light microscopy. New structures in the large glandular cells were detected, including concentric cytoplasmic laminae, basal vesicles, silver nitrate staining cytoplasmic granules, and a high affinity for wheat-germ agglutinin lectin in the cytoplasm of mature large glandular cells.We also describe morphologic changes of the venom gland during thermal test. At low temperatures, the large glandular cells and their nuclei become enlarged, whereas at high temperatures the large glandular cells are smaller and their nuclei irregular in shape. Similarly, samples from fish captured during two opposite seasons showed differences in their nuclei, which were smaller in summer than winter. The larger growth of supporting cells at low temperatures, together with their aggregation during conditions of stress and their vacuoles secretion, suggest that supporting cells could be played several roles.</p></div>
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The structure of the venom gland of Trachinus draco was studied by histological techniques using light microscopy. New structures in the large glandular cells were detected, including concentric cytoplasmic laminae, basal vesicles, silver nitrate staining cytoplasmic granules, and a high affinity for wheat-germ agglutinin lectin in the cytoplasm of mature large glandular cells.We also describe morphologic changes of the venom gland during thermal test. At low temperatures, the large glandular cells and their nuclei become enlarged, whereas at high temperatures the large glandular cells are smaller and their nuclei irregular in shape. Similarly, samples from fish captured during two opposite seasons showed differences in their nuclei, which were smaller in summer than winter. The larger growth of supporting cells at low temperatures, together with their aggregation during conditions of stress and their vacuoles secretion, suggest that supporting cells could be played several roles.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12003" xmlns="http://purl.org/rss/1.0/"><title>Comparative immunolocalization of keratin-associated beta-proteins (beta-keratins) supports a new explanation for the cyclical process of keratinocyte differentiation in lizard epidermis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12003</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparative immunolocalization of keratin-associated beta-proteins (beta-keratins) supports a new explanation for the cyclical process of keratinocyte differentiation in lizard epidermis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lorenzo Alibardi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-10-17T00:57:00.125043-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12003</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12003</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12003</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Lizard epidermis is made of beta- and alpha-layers. Using Western blot tested antibodies, the ultrastructural immunolocalization of specific keratin-associated beta-proteins in the epidermis of different lizard species reveals that glycine-rich beta-proteins (HgG5) localize in the beta-layer, while glycine–cysteine-medium-rich beta-proteins (HgGC10) are present in oberhautchen and alpha-layers. This suggests a new explanation for the formation of different epidermal layers during the shedding cycle in lepidosaurian epidermis instead of an alternance between beta-keratins and alpha-keratins. It is proposed that different sets of genes coding for specific beta-proteins are activated in keratinocytes during the renewal phase of the shedding cycle. Initially, glycine–cysteine-medium-rich beta-proteins with hydrophilic and elastic properties accumulate over alpha-keratins in the oberhautchen but are replaced in the next cell layer with glycine-rich hydrophobic beta-proteins forming a resistant, stiff, and hydrophobic beta-layer. The synthesis of glycine-rich proteins terminates in mesos and alpha-cells where these proteins are replaced with glycine–cysteine-rich beta-proteins. The pattern of beta-protein deposition onto a scaffold of intermediate filament keratins is typical for keratin-associated proteins and the association between alpha-keratins and specific keratin-associated beta-proteins during the renewal phase of the shedding cycle gives rise to epidermal layers possessing different structural, mechanical, and texture properties.</p></div>
]]></content:encoded><description>

Lizard epidermis is made of beta- and alpha-layers. Using Western blot tested antibodies, the ultrastructural immunolocalization of specific keratin-associated beta-proteins in the epidermis of different lizard species reveals that glycine-rich beta-proteins (HgG5) localize in the beta-layer, while glycine–cysteine-medium-rich beta-proteins (HgGC10) are present in oberhautchen and alpha-layers. This suggests a new explanation for the formation of different epidermal layers during the shedding cycle in lepidosaurian epidermis instead of an alternance between beta-keratins and alpha-keratins. It is proposed that different sets of genes coding for specific beta-proteins are activated in keratinocytes during the renewal phase of the shedding cycle. Initially, glycine–cysteine-medium-rich beta-proteins with hydrophilic and elastic properties accumulate over alpha-keratins in the oberhautchen but are replaced in the next cell layer with glycine-rich hydrophobic beta-proteins forming a resistant, stiff, and hydrophobic beta-layer. The synthesis of glycine-rich proteins terminates in mesos and alpha-cells where these proteins are replaced with glycine–cysteine-rich beta-proteins. The pattern of beta-protein deposition onto a scaffold of intermediate filament keratins is typical for keratin-associated proteins and the association between alpha-keratins and specific keratin-associated beta-proteins during the renewal phase of the shedding cycle gives rise to epidermal layers possessing different structural, mechanical, and texture properties.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00578.x" xmlns="http://purl.org/rss/1.0/"><title>Skin structure and hair morphology of different body parts in the Common Pipistrelle (Pipistrellus pipistrellus)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00578.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Skin structure and hair morphology of different body parts in the Common Pipistrelle (Pipistrellus pipistrellus)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jan P. Madej, Lucie Mikulová, Alexandra Gorošová, Štěpán Mikula, Zdeněk Řehák, František Tichý, Marcela Buchtová</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-18T03:12:00.66162-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00578.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00578.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00578.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The bat skin shows an unusual morphology that corresponds to flying adaptations but also performs multiple functions including a protective barrier against microbes and parasites. Here, we compare the microscopic structure of the skin and hairs collected from the membranes with other body parts in the Common Pipistrelle (<em>Pipistrellus pipistrellus</em>) in relation to parasite availability. Statistical analysis of whole-skin thickness revealed two main groups according to body regions; the first with thin skin (wing and tail membrane) and the second with thick skin (head and dorsum, abdomen, footpad). The density of hair was evaluated by a novel method, and it revealed that the density was significantly higher in the head region than in dorsal and ventral body parts. These differences possibly play a role for bat ectoparasites when choosing the preferred region of their host. Along the axis of each hair, the scale morphology was found to be variable. Hair morphology, however, did not vary among body regions. Mast cells were numerous in the hairy areas around vessels and hair follicles of the dorsum and abdomen, which are easily accessible to ectoparasites. Increased numbers of mast cells in hair-bearing skin are part of the host adaptation system in parasite-preferred locations.</p></div>
]]></content:encoded><description>

The bat skin shows an unusual morphology that corresponds to flying adaptations but also performs multiple functions including a protective barrier against microbes and parasites. Here, we compare the microscopic structure of the skin and hairs collected from the membranes with other body parts in the Common Pipistrelle (Pipistrellus pipistrellus) in relation to parasite availability. Statistical analysis of whole-skin thickness revealed two main groups according to body regions; the first with thin skin (wing and tail membrane) and the second with thick skin (head and dorsum, abdomen, footpad). The density of hair was evaluated by a novel method, and it revealed that the density was significantly higher in the head region than in dorsal and ventral body parts. These differences possibly play a role for bat ectoparasites when choosing the preferred region of their host. Along the axis of each hair, the scale morphology was found to be variable. Hair morphology, however, did not vary among body regions. Mast cells were numerous in the hairy areas around vessels and hair follicles of the dorsum and abdomen, which are easily accessible to ectoparasites. Increased numbers of mast cells in hair-bearing skin are part of the host adaptation system in parasite-preferred locations.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12001" xmlns="http://purl.org/rss/1.0/"><title>
Embryos in Deep Time, the Rock Record of Biological Development Sánchez, M.University of California Press, Berkeley, 256 pp, ISBN978-0-520-27193-7, Price $39.95.
</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12001</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">
Embryos in Deep Time, the Rock Record of Biological Development Sánchez, M.University of California Press, Berkeley, 256 pp, ISBN978-0-520-27193-7, Price $39.95.
</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. G. M. Thewissen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-18T00:17:50.80763-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12001</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12001</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12001</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Book Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00572.x" xmlns="http://purl.org/rss/1.0/"><title>Morphology of the female reproductive organs of the African lion (Panthera leo)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00572.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Morphology of the female reproductive organs of the African lion (Panthera leo)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marthinus J. Hartman, Hermanus B. Groenewald, Robert M. Kirberger</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-25T00:09:46.188148-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00572.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00572.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00572.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The topography and splanchnology of the reproductive organs of the African lioness were studied and described <em>in situ</em> and after removal. The kidneys were located far caudally in relation to the thirteenth ribs. The suspensory ligament was very well developed, originated in a fan-like manner from the dorsolateral abdominal wall lateral to the kidney and extended up to a few centimetres cranial to the kidney. The proper ligament of the ovary as well as the round ligament was well developed. The round ligament inserted on the medial femoral fascia. The left ovary was bigger than the right. The ovarian bursa had a short mesosalpinx that did not cover any part of the ovary and the fimbriae extended along the entire length. The urethral tuberculum as well as the urethral crest were well developed. The left uterine horn was longer than the right. The uterine tube was found to open directly into the tip of the uterine horn and not onto a papilla. The reproductive organs of the lioness resembled those of the domestic cat and dog but with some major differences.</p></div>]]></content:encoded><description>The topography and splanchnology of the reproductive organs of the African lioness were studied and described in situ and after removal. The kidneys were located far caudally in relation to the thirteenth ribs. The suspensory ligament was very well developed, originated in a fan-like manner from the dorsolateral abdominal wall lateral to the kidney and extended up to a few centimetres cranial to the kidney. The proper ligament of the ovary as well as the round ligament was well developed. The round ligament inserted on the medial femoral fascia. The left ovary was bigger than the right. The ovarian bursa had a short mesosalpinx that did not cover any part of the ovary and the fimbriae extended along the entire length. The urethral tuberculum as well as the urethral crest were well developed. The left uterine horn was longer than the right. The uterine tube was found to open directly into the tip of the uterine horn and not onto a papilla. The reproductive organs of the lioness resembled those of the domestic cat and dog but with some major differences.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00577.x" xmlns="http://purl.org/rss/1.0/"><title>Histological and histochemical study of the duodenum of the plains viscacha (Lagostomus maximus) at different stages of its ontogenetic development</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00577.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Histological and histochemical study of the duodenum of the plains viscacha (Lagostomus maximus) at different stages of its ontogenetic development</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">María Florencia Tano de la Hoz, Mirta Alicia Flamini, Alcira Ofelia Díaz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-19T23:31:33.83191-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00577.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00577.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00577.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The general objective of this study focused on the duodenal histological and histochemical analysis of fetuses and adults of plains viscacha (<em>Lagostomus maximus</em>) from the Buenos Aires province (Argentina). Histological techniques, histochemical procedures for localizing and characterizing glycoproteins (GPs) and lectin histochemical techniques for the identification of specific sugar residues were used. The duodenal structure of all age groups here considered was typical of mammals. We identified a proliferation phase and an epithelial morphogenesis in mid-gestational fetuses, an intermediate period of cell differentiation in at-term fetuses and a posterior stage of physiological maturation in adults. According to histochemistry, the diverse GPs elaborated and secreted into the duodenum show a high degree of histochemical complexity related to the multiple functions of mucus in the digestive tract. The GPs in the duodenum of <em>L. maximus</em> and their glycosylation patterns varied according to the animal's age and the developmental state of the organ.</p></div>]]></content:encoded><description>The general objective of this study focused on the duodenal histological and histochemical analysis of fetuses and adults of plains viscacha (Lagostomus maximus) from the Buenos Aires province (Argentina). Histological techniques, histochemical procedures for localizing and characterizing glycoproteins (GPs) and lectin histochemical techniques for the identification of specific sugar residues were used. The duodenal structure of all age groups here considered was typical of mammals. We identified a proliferation phase and an epithelial morphogenesis in mid-gestational fetuses, an intermediate period of cell differentiation in at-term fetuses and a posterior stage of physiological maturation in adults. According to histochemistry, the diverse GPs elaborated and secreted into the duodenum show a high degree of histochemical complexity related to the multiple functions of mucus in the digestive tract. The GPs in the duodenum of L. maximus and their glycosylation patterns varied according to the animal's age and the developmental state of the organ.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00576.x" xmlns="http://purl.org/rss/1.0/"><title>Comparative morphology of the pectoral fin spine of the Persian sturgeon Acipenser persicus, the Russian sturgeon Acipenser gueldenstaedtii, and the Starry sturgeon Acipenser stellatus in Iranian waters of the Caspian Sea</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00576.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparative morphology of the pectoral fin spine of the Persian sturgeon Acipenser persicus, the Russian sturgeon Acipenser gueldenstaedtii, and the Starry sturgeon Acipenser stellatus in Iranian waters of the Caspian Sea</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shima Bakhshalizadeh, Ali Bani, Shahram Abdolmalaki</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-10T04:36:47.578362-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00576.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00576.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00576.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The morphological characteristics of the pectoral fin spine were compared in three species of sturgeon, the Persian sturgeon (<em>Acipenser persicus</em>), the Russian sturgeon (<em>Acipenser gueldenstaedtii</em>), and the Starry sturgeon (<em>Acipenser stellatus</em>), all sampled from the Caspian Sea. On the basis of morphological characters of the pectoral fin spine, 62.2% of the individuals were correctly classified into separate groups. The cluster analysis also divided the three species into two major subgroups. <em>Acipenser persicus</em> and <em>A. gueldenstaedtii</em> were grouped together, suggesting a similar evolutionary basis. Significant morphological heterogeneity in pectoral fin spine characteristics was observed among the three sturgeon species. Principal component analysis identified the largest differences were in the pectoral fin spine size and the angle between distal pectoral fin spine and the horizontal line (A°). The first and second principal components (PC1 and PC2) of all observations accounted for 64.19% and 14.33% of the total variation, respectively. The combination of all analyses showed the relevance of applying pectoral fin spine shape for interspecific distinction of the three species of sturgeons.</p></div>]]></content:encoded><description>The morphological characteristics of the pectoral fin spine were compared in three species of sturgeon, the Persian sturgeon (Acipenser persicus), the Russian sturgeon (Acipenser gueldenstaedtii), and the Starry sturgeon (Acipenser stellatus), all sampled from the Caspian Sea. On the basis of morphological characters of the pectoral fin spine, 62.2% of the individuals were correctly classified into separate groups. The cluster analysis also divided the three species into two major subgroups. Acipenser persicus and A. gueldenstaedtii were grouped together, suggesting a similar evolutionary basis. Significant morphological heterogeneity in pectoral fin spine characteristics was observed among the three sturgeon species. Principal component analysis identified the largest differences were in the pectoral fin spine size and the angle between distal pectoral fin spine and the horizontal line (A°). The first and second principal components (PC1 and PC2) of all observations accounted for 64.19% and 14.33% of the total variation, respectively. The combination of all analyses showed the relevance of applying pectoral fin spine shape for interspecific distinction of the three species of sturgeons.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00573.x" xmlns="http://purl.org/rss/1.0/"><title>Microvascular anatomy of the esophagus in larval and adult Xenopus laevis Daudin: a scanning electron microscope study of microvascular corrosion casts and correlative light microscopy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00573.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Microvascular anatomy of the esophagus in larval and adult Xenopus laevis Daudin: a scanning electron microscope study of microvascular corrosion casts and correlative light microscopy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alois Lametschwandtner, Heidi Bartel, Bernd Minnich</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-06T01:54:35.947295-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00573.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00573.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00573.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Larval to adult microvascular anatomy of the esophagus was studied in the South African Clawed Toad, <em>Xenopus laevis</em> (Daudin) by scanning electron microscopy of vascular corrosion casts and correlative light microscopy of paraplast embedded stained tissue sections. Analyses of vascular corrosion casts of tadpole esophaguses at premetamorphosis revealed a wide-meshed, but mature looking capillary bed which during following prometamorphosis increased in density and gained the adult-like pattern during late metamorphic climax by sprouting and nonsprouting angiogenesis. In adult <em>Xenopus,</em> the esophageal mucosa possessed a dense subepithelial capillary bed fed by one or two esophageal arteries that originated from right and/or left thoracic aorta just distal to the origin of the subclavian arteries. In the adult undistended esophagus, esophageal arteries revealed an undulating course, a pattern that guarantees a continuous blood supply when the esophagus is extremely wide expanded as it is the case when adult <em>Xenopus</em> swallows large prey.</p></div>]]></content:encoded><description>Larval to adult microvascular anatomy of the esophagus was studied in the South African Clawed Toad, Xenopus laevis (Daudin) by scanning electron microscopy of vascular corrosion casts and correlative light microscopy of paraplast embedded stained tissue sections. Analyses of vascular corrosion casts of tadpole esophaguses at premetamorphosis revealed a wide-meshed, but mature looking capillary bed which during following prometamorphosis increased in density and gained the adult-like pattern during late metamorphic climax by sprouting and nonsprouting angiogenesis. In adult Xenopus, the esophageal mucosa possessed a dense subepithelial capillary bed fed by one or two esophageal arteries that originated from right and/or left thoracic aorta just distal to the origin of the subclavian arteries. In the adult undistended esophagus, esophageal arteries revealed an undulating course, a pattern that guarantees a continuous blood supply when the esophagus is extremely wide expanded as it is the case when adult Xenopus swallows large prey.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00575.x" xmlns="http://purl.org/rss/1.0/"><title>Effect of long-term injection of dopamine on the ovarian growth of Cherax quadricarinatus juvenile females (Parastacidae, Decapoda)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00575.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effect of long-term injection of dopamine on the ovarian growth of Cherax quadricarinatus juvenile females (Parastacidae, Decapoda)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carolina Tropea, Laura S. López Greco</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-03T07:10:38.704314-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00575.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00575.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00575.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The neurotransmitter dopamine (DA) modulates many physiological processes in decapod crustaceans, including reproduction. This study was aimed at evaluating whether the long-term injection of DA affects ovarian growth in the freshwater crayfish <em>Cherax quadricarinatus</em>. Three experiments were performed with females of different mean initial size: 4.15 g (Group A); 9.65 g (Group B); and 13.98 g (Group C). Treated females were injected with DA and control females with physiological saline twice a week for 90 (Group B), 105 (Group A) and 120 (Group C) days. At the end of the experiments, the animals were killed, and the stage of ovarian development, gonadosomatic index, and mean oocyte diameter were determined. DA had a differential effect according to female size: it negatively affected ovarian growth of females in a weight range of 4–14 g and had no effect on ovarian maturation when injected to females with an initial weight of 14 g. The results are compared with previous reports in freshwater decapod crustaceans.</p></div>]]></content:encoded><description>The neurotransmitter dopamine (DA) modulates many physiological processes in decapod crustaceans, including reproduction. This study was aimed at evaluating whether the long-term injection of DA affects ovarian growth in the freshwater crayfish Cherax quadricarinatus. Three experiments were performed with females of different mean initial size: 4.15 g (Group A); 9.65 g (Group B); and 13.98 g (Group C). Treated females were injected with DA and control females with physiological saline twice a week for 90 (Group B), 105 (Group A) and 120 (Group C) days. At the end of the experiments, the animals were killed, and the stage of ovarian development, gonadosomatic index, and mean oocyte diameter were determined. DA had a differential effect according to female size: it negatively affected ovarian growth of females in a weight range of 4–14 g and had no effect on ovarian maturation when injected to females with an initial weight of 14 g. The results are compared with previous reports in freshwater decapod crustaceans.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00574.x" xmlns="http://purl.org/rss/1.0/"><title>Reproductive morphology of the male Tuatara, Sphenodon punctatus</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00574.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reproductive morphology of the male Tuatara, Sphenodon punctatus</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Justin L. Rheubert, Alison Cree, Matthew Downes, David M. Sever</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-03T07:10:21.71888-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00574.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00574.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00574.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Over the past decade, studies on reproductive morphology in the Squamata (snakes and lizards) have expanded tremendously. With the accumulation of these studies and revisions of the terminology based on structural similarities and differences, it is imperative to review the work on tuataras to determine whether the structural organization fits the revised terminology of vertebrates. We investigated the morphology of the male reproductive system in the Tuatara, <em>Sphenodon punctatus</em> (Rhynchocephalia), the sister taxon to the Squamata. Previous studies on the Tuatara used a nomenclature for the testicular ducts different from the current terminology for amniotes. The reproductive system in the Tuatara is consistent with reports in the Squamata. Two rete testis tubules exit the testis within a connective tissue sheath similar to that shown in other squamate species and the protherian Echidna. Each rete testis divides into multiple ductuli efferentes that fuse with the epididymis. The epididymis transitions into the ductus deferens where the sperm become more concentrated into spherical bundles. The ductus deferens enters the cloacal urodeum separately from the ureter. An ampulla ureter or ampulla urogenital papilla was not observed, which differs from previous studies of lepidosaurians. Furthermore, a sexual segment of the kidney (SSK) was not observed, consistent with previous studies on the Tuatara.</p></div>]]></content:encoded><description>Over the past decade, studies on reproductive morphology in the Squamata (snakes and lizards) have expanded tremendously. With the accumulation of these studies and revisions of the terminology based on structural similarities and differences, it is imperative to review the work on tuataras to determine whether the structural organization fits the revised terminology of vertebrates. We investigated the morphology of the male reproductive system in the Tuatara, Sphenodon punctatus (Rhynchocephalia), the sister taxon to the Squamata. Previous studies on the Tuatara used a nomenclature for the testicular ducts different from the current terminology for amniotes. The reproductive system in the Tuatara is consistent with reports in the Squamata. Two rete testis tubules exit the testis within a connective tissue sheath similar to that shown in other squamate species and the protherian Echidna. Each rete testis divides into multiple ductuli efferentes that fuse with the epididymis. The epididymis transitions into the ductus deferens where the sperm become more concentrated into spherical bundles. The ductus deferens enters the cloacal urodeum separately from the ureter. An ampulla ureter or ampulla urogenital papilla was not observed, which differs from previous studies of lepidosaurians. Furthermore, a sexual segment of the kidney (SSK) was not observed, consistent with previous studies on the Tuatara.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00571.x" xmlns="http://purl.org/rss/1.0/"><title>Ontogeny and tissue differentiation of the pelvic girdle and hind limbs of anurans</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00571.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ontogeny and tissue differentiation of the pelvic girdle and hind limbs of anurans</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adriana Manzano, Virginia Abdala, María L. Ponssa, Mónica Soliz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-06-29T04:31:24.737697-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00571.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00571.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00571.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We present the ontogeny of the integrated musculoskeletal complex that comprises the pelvic girdle and hind limbs of anurans. Our histological data show that the pelvic girdle originates from a single mesenchymatic condensation. The tissue differentiation sequence is cartilage, muscle and tendon. The intrusion of the ischiadic nerve into the limb bud is produced very early in ontogeny. The pre-cartilage appears in the pre-motile stage. Therefore, the nerve produces a movement analogous to the ‘embryonic motility’ that would induce the emergence of the pre-cartilage. The acetabulum is the first of all cavitation processes to form, the second one being the knee. The acetabulum appears before the muscles are mature, although it has been stressed that the muscle contraction maintains joint progenitors committed to their fate. Our data indicate an explosive differentiation of all 11 muscular masses together. We provide three new characters that support the monophyly of Hyloides, Acosmanura and Neobatrachia.</p></div>]]></content:encoded><description>We present the ontogeny of the integrated musculoskeletal complex that comprises the pelvic girdle and hind limbs of anurans. Our histological data show that the pelvic girdle originates from a single mesenchymatic condensation. The tissue differentiation sequence is cartilage, muscle and tendon. The intrusion of the ischiadic nerve into the limb bud is produced very early in ontogeny. The pre-cartilage appears in the pre-motile stage. Therefore, the nerve produces a movement analogous to the ‘embryonic motility’ that would induce the emergence of the pre-cartilage. The acetabulum is the first of all cavitation processes to form, the second one being the knee. The acetabulum appears before the muscles are mature, although it has been stressed that the muscle contraction maintains joint progenitors committed to their fate. Our data indicate an explosive differentiation of all 11 muscular masses together. We provide three new characters that support the monophyly of Hyloides, Acosmanura and Neobatrachia.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00570.x" xmlns="http://purl.org/rss/1.0/"><title>Animal Eyes 2nd edn. Land, M. F. and Nilsson, D.-E. (2012). Oxford University Press, Oxford, 271 pp, Hardback GBP 65.00, Paperback GBP 32,50. ISBN 978-0-19-958114-6.</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00570.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Animal Eyes 2nd edn. Land, M. F. and Nilsson, D.-E. (2012). Oxford University Press, Oxford, 271 pp, Hardback GBP 65.00, Paperback GBP 32,50. ISBN 978-0-19-958114-6.</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Roland R Melzer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-06-20T01:25:24.894834-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00570.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00570.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00570.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Book Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00567.x" xmlns="http://purl.org/rss/1.0/"><title>Cnidae in the sea anemone Sagartiogeton viduatus (Muller, 1776) (Cnidaria, Anthozoa); A comparison to cnidae in the sea anemone Metridium senile (Linnaeus, 1761) (Cnidaria, Anthozoa)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00567.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cnidae in the sea anemone Sagartiogeton viduatus (Muller, 1776) (Cnidaria, Anthozoa); A comparison to cnidae in the sea anemone Metridium senile (Linnaeus, 1761) (Cnidaria, Anthozoa)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carina Östman, Fredrik Borg, Carsten Roat, Jens Roat Kultima, Sau Yu Grace Wong</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-05-27T22:58:09.226539-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00567.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00567.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00567.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The cnidom of the sea anemone <em>Sagartiogeton viduatus</em> (Muller, 1776) is described from interference-contrast light micrographs (LMs) and scanning electron micrographs (SEMs). Special attention is given to nematocyst maturation, including the differentiation of the shaft into proximal and main regions as helical folding of the shaft wall proceeds. Comparisons are made with <em>Metridium senile</em> (Linnaeus, 1761), whose cnidom, with a few exceptions, is closely similar to that of <em>S. viduatus</em>. The two anemones possess b- and p-mastigophores, p-amastigophores, isorhizas and spirocysts. Although the majority of cnidae in <em>S. viduatus</em> is smaller than corresponding ones in <em>M. senile</em>, they are grouped into the same size classes as those of <em>M. senile</em>, namely small, medium and large. The main differences from <em>M. senile</em> cnidae are the followings: (1) Large acontia p-amastigophores are the largest nematocysts in <em>S. viduatus</em>. (2) They are noticeably larger than the large acontia b-mastigophores, and (3) they are separated from the p-amastigophores of <em>M. senile</em> by the sinusoid pattern of their U-shaped capsular matrix. (4) The large acontia b-mastigophores are microbasic and not mesobasic as in <em>M. Senile</em>, and (5) they do not produce darts. (6) Another difference from <em>M. senile</em> is the absence of catch-tentacle isorhizas.</p></div>]]></content:encoded><description>The cnidom of the sea anemone Sagartiogeton viduatus (Muller, 1776) is described from interference-contrast light micrographs (LMs) and scanning electron micrographs (SEMs). Special attention is given to nematocyst maturation, including the differentiation of the shaft into proximal and main regions as helical folding of the shaft wall proceeds. Comparisons are made with Metridium senile (Linnaeus, 1761), whose cnidom, with a few exceptions, is closely similar to that of S. viduatus. The two anemones possess b- and p-mastigophores, p-amastigophores, isorhizas and spirocysts. Although the majority of cnidae in S. viduatus is smaller than corresponding ones in M. senile, they are grouped into the same size classes as those of M. senile, namely small, medium and large. The main differences from M. senile cnidae are the followings: (1) Large acontia p-amastigophores are the largest nematocysts in S. viduatus. (2) They are noticeably larger than the large acontia b-mastigophores, and (3) they are separated from the p-amastigophores of M. senile by the sinusoid pattern of their U-shaped capsular matrix. (4) The large acontia b-mastigophores are microbasic and not mesobasic as in M. Senile, and (5) they do not produce darts. (6) Another difference from M. senile is the absence of catch-tentacle isorhizas.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00569.x" xmlns="http://purl.org/rss/1.0/"><title>Characterization of mature testis and sperm morphology of Gymnotus carapo (Gymnotidae, Teleostei) from the southeast of Brazil</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00569.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Characterization of mature testis and sperm morphology of Gymnotus carapo (Gymnotidae, Teleostei) from the southeast of Brazil</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cristiane dos S. Vergílio, Renata V. Moreira, Carlos E.V. Carvalho, Edésio J.T. Melo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-05-22T21:32:40.937671-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00569.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00569.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00569.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The present study examined the testicular structure and sperm morphology of freshwater fish <em>Gymnotus carapo</em>. Testicular structure and sperm morphology were analyzed using light, transmission and scanning electron microscopy. Anatomically, the testes weighed 0.070 ± 0.01 g and were oval with a yellow-white color. The <em>G. caparo</em> testis is organized in interstitial and tubular compartments. Spermatogenesis occurs in seminiferous tubules where the germinal epithelium is organized in spermatogenic cystis. Germ cells are seen in different stages of differentiation: type A (SPGA) and type B (SPGB) spermatogonia, primary (SPCI) and secondary (SPCII) spermatocytes, and spermatids (SPD). Differentiated spermatozoa (SZ) are seen within the cysts, characterized by a round head, a short midpiece, and a single flagellum with absence of acrosome. Spermatids were seen in the lumen of the testicular tubules together with spermatozoa, suggesting that spermatogenesis is of the semicystic type. The present study shows that <em>G. carapo</em> has an anastomosing tubular type of testis with an unrestricted distribution of the spermatogonia and semicystic type of spermatogenesis. Sperm structure follows the general pattern described for other teleostei species. These descriptions are important for a better understanding of reproductive biology and phylogeny, particularly of tropical fishes, for which data remain scarce in the literature.</p></div>]]></content:encoded><description>The present study examined the testicular structure and sperm morphology of freshwater fish Gymnotus carapo. Testicular structure and sperm morphology were analyzed using light, transmission and scanning electron microscopy. Anatomically, the testes weighed 0.070 ± 0.01 g and were oval with a yellow-white color. The G. caparo testis is organized in interstitial and tubular compartments. Spermatogenesis occurs in seminiferous tubules where the germinal epithelium is organized in spermatogenic cystis. Germ cells are seen in different stages of differentiation: type A (SPGA) and type B (SPGB) spermatogonia, primary (SPCI) and secondary (SPCII) spermatocytes, and spermatids (SPD). Differentiated spermatozoa (SZ) are seen within the cysts, characterized by a round head, a short midpiece, and a single flagellum with absence of acrosome. Spermatids were seen in the lumen of the testicular tubules together with spermatozoa, suggesting that spermatogenesis is of the semicystic type. The present study shows that G. carapo has an anastomosing tubular type of testis with an unrestricted distribution of the spermatogonia and semicystic type of spermatogenesis. Sperm structure follows the general pattern described for other teleostei species. These descriptions are important for a better understanding of reproductive biology and phylogeny, particularly of tropical fishes, for which data remain scarce in the literature.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00568.x" xmlns="http://purl.org/rss/1.0/"><title>Jaw musculature of the Meiglyptini (Aves: Piciformes: Picidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00568.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Jaw musculature of the Meiglyptini (Aves: Piciformes: Picidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Reginaldo J. Donatelli</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-05-14T08:17:04.153227-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00568.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00568.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00568.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The Meiglyptini comprise eight species of woodpeckers grouped into three genera, two of which contain three species (<em>Meiglyptes</em> and <em>Mulleripicus</em>), while one genus includes two species (<em>Hemicircus</em>). The purpose of this study is to describe the mandibular apparatus found in six species of Meiglyptini and to compare them with each other and with other woodpecker species. The results reveal a number of structures that are worth mentioning: (i) the components of the external mandibular adductor system of <em>Hemicircus concretus</em>, particularly the <em>M. adductor mandibulae externus caudalis medialis</em>, are underdeveloped compared with the other investigated species; (ii) the muscles of the internal mandibular system are structurally different among <em>Meiglyptes</em> species and are less developed, both in size and in structure, in <em>H. concretus</em>; (iii) the <em>M</em>. <em>protractor quadrati</em> is vestigial in <em>Meiglyptes</em> species; (iv) the muscles of the protractor system of the quadrate are relatively undeveloped in <em>H. concretus</em>; (v) most of the muscles of the <em>pterygoideus</em> system are structurally differentiated in <em>Meiglyptes</em> species. It appears that the complexity of the mandibular apparatus is associated with the type of food consumed, as the apparatus of the frugivorous species <em>H. concretus</em> is markedly different from that of the insectivorous species.</p></div>]]></content:encoded><description>The Meiglyptini comprise eight species of woodpeckers grouped into three genera, two of which contain three species (Meiglyptes and Mulleripicus), while one genus includes two species (Hemicircus). The purpose of this study is to describe the mandibular apparatus found in six species of Meiglyptini and to compare them with each other and with other woodpecker species. The results reveal a number of structures that are worth mentioning: (i) the components of the external mandibular adductor system of Hemicircus concretus, particularly the M. adductor mandibulae externus caudalis medialis, are underdeveloped compared with the other investigated species; (ii) the muscles of the internal mandibular system are structurally different among Meiglyptes species and are less developed, both in size and in structure, in H. concretus; (iii) the M. protractor quadrati is vestigial in Meiglyptes species; (iv) the muscles of the protractor system of the quadrate are relatively undeveloped in H. concretus; (v) most of the muscles of the pterygoideus system are structurally differentiated in Meiglyptes species. It appears that the complexity of the mandibular apparatus is associated with the type of food consumed, as the apparatus of the frugivorous species H. concretus is markedly different from that of the insectivorous species.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00566.x" xmlns="http://purl.org/rss/1.0/"><title>Histomorphological structure of the palate and histochemical profiles of the salivary palatine glands in the Chukar partridge (Alectoris chukar, Gray 1830)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00566.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Histomorphological structure of the palate and histochemical profiles of the salivary palatine glands in the Chukar partridge (Alectoris chukar, Gray 1830)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hakan Sağsöz, Serkan Erdoğan, Mehmet E. Akbalik</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-04-01T23:56:18.727276-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00566.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00566.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00566.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Morphology of the palatine mucosa and its secretion was described in Chukar partridges, by gross morphology and histochemistry techniques. For this purpose, 10 healthy adults (five male and five female) were sacrificed. After sacrifice, the palatine tissues were extirpated and fixed in 10% formol-alcohol for 18 h and were embedded longitudinally and transversally in paraffin. The 5-μm sections were employed histological and histochemical staining techniques. The lateral rims of the caudal part of the choanal cleft were bordered by large conical papillae. In the periphery of the choanal and the infundibular cleft, small papillae were scattered across the palatine mucosa. The palate was lined by keratinized stratified squamous epithelium, which contained conical papillae of varying height. However, the folds of the keratinized stratified squamous epithelial layer covering the choanal and infundibular cleft were nonkeratinized. The rostral aspect of the choanal cleft contained simple branched tubulo-alveolar glands of both mucous and sero-mucous characteristic, whilst the caudal aspect included mucous simple branched tubular glands. Furthermore, it was ascertained that the secretion of the palatine glands contained glycoproteins, carboxylated proteoglycans, weakly and strongly sulphated mucins, sialic acid and hyaluronic acid, but lacked glycogen. In conclusion, it was demonstrated that the histological structure of the mucosal epithelium and the supporting elements displayed similarity to those of other domestic avian species.</p></div>]]></content:encoded><description>Morphology of the palatine mucosa and its secretion was described in Chukar partridges, by gross morphology and histochemistry techniques. For this purpose, 10 healthy adults (five male and five female) were sacrificed. After sacrifice, the palatine tissues were extirpated and fixed in 10% formol-alcohol for 18 h and were embedded longitudinally and transversally in paraffin. The 5-μm sections were employed histological and histochemical staining techniques. The lateral rims of the caudal part of the choanal cleft were bordered by large conical papillae. In the periphery of the choanal and the infundibular cleft, small papillae were scattered across the palatine mucosa. The palate was lined by keratinized stratified squamous epithelium, which contained conical papillae of varying height. However, the folds of the keratinized stratified squamous epithelial layer covering the choanal and infundibular cleft were nonkeratinized. The rostral aspect of the choanal cleft contained simple branched tubulo-alveolar glands of both mucous and sero-mucous characteristic, whilst the caudal aspect included mucous simple branched tubular glands. Furthermore, it was ascertained that the secretion of the palatine glands contained glycoproteins, carboxylated proteoglycans, weakly and strongly sulphated mucins, sialic acid and hyaluronic acid, but lacked glycogen. In conclusion, it was demonstrated that the histological structure of the mucosal epithelium and the supporting elements displayed similarity to those of other domestic avian species.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00565.x" xmlns="http://purl.org/rss/1.0/"><title>Comparative study of sperm ultrastructure of Donax hanleyanus and Donax gemmula (Bivalvia: Donacidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00565.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparative study of sperm ultrastructure of Donax hanleyanus and Donax gemmula (Bivalvia: Donacidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gisele O. Introíni, Flávio D. Passos, Shirlei M. Recco-Pimentel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-30T01:18:45.460283-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00565.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00565.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00565.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The ultrastructure of bivalve spermatozoa can be species-specific and often provides important taxonomic traits for systematic reviews and phylogenetic reconstructions. Young individuals of the Donacidae species <em>Donax hanleyanus</em> are often identified as samples of <em>Donax gemmula</em>. Hence, the spermatozoa ultrastructure of both species was described in the present work, aiming to identify characters that could be useful for further taxonomic and phylogenetic analyses. <em>D. hanleyanus</em> and <em>D. gemmula</em> spermatozoa were different especially in relation to acrosomal characteristics and chromatin condensation. The spermatozoon produced by <em>D. hanleyanus</em> had a nucleus (exhibiting granular chromatin with a rope-like appearance) capped by a long and conical acrosomal vesicle, which extended itself outward beyond the anterior nuclear fossa. Otherwise, the nucleus of the sperm cell of <em>D. gemmula</em> showed well-compacted chromatin, and its acrosome, which was partially inserted into the anterior nuclear fossa, had a bubble-like tip. In conclusion, the conspicuous ultra-structural differences found between the spermatozoan morphologies were helpful for the discrimination of the species. In conclusion, our results suggest that analyses of sperm ultrastructure of the bivalves in the family Donacidae can be valuable to investigate their taxonomic relatedness. The present results also contribute to assess the monophyletic status of the family.</p></div>]]></content:encoded><description>The ultrastructure of bivalve spermatozoa can be species-specific and often provides important taxonomic traits for systematic reviews and phylogenetic reconstructions. Young individuals of the Donacidae species Donax hanleyanus are often identified as samples of Donax gemmula. Hence, the spermatozoa ultrastructure of both species was described in the present work, aiming to identify characters that could be useful for further taxonomic and phylogenetic analyses. D. hanleyanus and D. gemmula spermatozoa were different especially in relation to acrosomal characteristics and chromatin condensation. The spermatozoon produced by D. hanleyanus had a nucleus (exhibiting granular chromatin with a rope-like appearance) capped by a long and conical acrosomal vesicle, which extended itself outward beyond the anterior nuclear fossa. Otherwise, the nucleus of the sperm cell of D. gemmula showed well-compacted chromatin, and its acrosome, which was partially inserted into the anterior nuclear fossa, had a bubble-like tip. In conclusion, the conspicuous ultra-structural differences found between the spermatozoan morphologies were helpful for the discrimination of the species. In conclusion, our results suggest that analyses of sperm ultrastructure of the bivalves in the family Donacidae can be valuable to investigate their taxonomic relatedness. The present results also contribute to assess the monophyletic status of the family.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00563.x" xmlns="http://purl.org/rss/1.0/"><title>Histological structure of the female gonads and ovipositor of the European bitterling, Rhodeus amarus (Bloch, 1782) (Cyprinidae: Acheilognathinae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00563.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Histological structure of the female gonads and ovipositor of the European bitterling, Rhodeus amarus (Bloch, 1782) (Cyprinidae: Acheilognathinae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anna V. Khlopova, Sergey Kul'bachnyi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T08:48:43.346968-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00563.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00563.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00563.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We investigated the histological structure of the female gonads and ovipositor of the European bitterling, <em>Rhodeus amarus</em>. The base of the ovipositor was formed by the conical organ or ‘eminence’. Based on the structure of the conical organ, including a special distribution of collagenous and muscular fibrils, a well-developed vascular system and numerous scyphoid mucous cells in the internal epithelium, this organ was used for temporary storage of oocytes during the spawning period and for their movement along the ovipositor. An extensive network of blood vessels, muscular fibrils and numerous collagenous fibrils in the connective tissue of the ovipositor may make a functional contribution to the ovipositor by making it firmer during egg laying. Mucous cells were detected in the medial and distal regions of the ovipositor, which may play a role in facilitating insertion of the ovipositor into the exhalant siphon of a mussel during oviposition. European bitterling are batch spawners, and the female spawns eggs in clutches at intervals during the breeding season, which were visible as three distinct cohorts of oocytes in the ovary.</p></div>]]></content:encoded><description>We investigated the histological structure of the female gonads and ovipositor of the European bitterling, Rhodeus amarus. The base of the ovipositor was formed by the conical organ or ‘eminence’. Based on the structure of the conical organ, including a special distribution of collagenous and muscular fibrils, a well-developed vascular system and numerous scyphoid mucous cells in the internal epithelium, this organ was used for temporary storage of oocytes during the spawning period and for their movement along the ovipositor. An extensive network of blood vessels, muscular fibrils and numerous collagenous fibrils in the connective tissue of the ovipositor may make a functional contribution to the ovipositor by making it firmer during egg laying. Mucous cells were detected in the medial and distal regions of the ovipositor, which may play a role in facilitating insertion of the ovipositor into the exhalant siphon of a mussel during oviposition. European bitterling are batch spawners, and the female spawns eggs in clutches at intervals during the breeding season, which were visible as three distinct cohorts of oocytes in the ovary.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00564.x" xmlns="http://purl.org/rss/1.0/"><title>Functional morphology of the mandibular gland of queens of the ant Monomorium pharaonis (L.)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00564.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Functional morphology of the mandibular gland of queens of the ant Monomorium pharaonis (L.)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sofie Boonen, Dieter Eelen, Lisbeth Børgesen, Johan Billen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T07:31:09.983252-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00564.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00564.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00564.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In this study, the functional morphology of the mandibular glands of pharaoh ant queens is investigated through histological and behavioural observations. The mandibular glands of queens of different age stages and mating status were examined at the light microscopical as well as the ultrastructural level. The results clearly show a high activity of the gland at the time of hatching, followed by a rapid degeneration independent of the queens' mating status. We therefore hypothesize the glandular secretion serves to stimulate workers to remove the queens' pupal skin. Experiments to compare hatching ability of isolated pupae and pupae assisted by workers confirmed the necessity of worker assistance, which is even more crucial to allow proper wing formation in queens and males. Together with the histological data, this suggests that the mandibular gland may indeed play a role in the social facilitation of hatching, although bioassays are required to give decisive answers about the mandibular gland's function.</p></div>]]></content:encoded><description>In this study, the functional morphology of the mandibular glands of pharaoh ant queens is investigated through histological and behavioural observations. The mandibular glands of queens of different age stages and mating status were examined at the light microscopical as well as the ultrastructural level. The results clearly show a high activity of the gland at the time of hatching, followed by a rapid degeneration independent of the queens' mating status. We therefore hypothesize the glandular secretion serves to stimulate workers to remove the queens' pupal skin. Experiments to compare hatching ability of isolated pupae and pupae assisted by workers confirmed the necessity of worker assistance, which is even more crucial to allow proper wing formation in queens and males. Together with the histological data, this suggests that the mandibular gland may indeed play a role in the social facilitation of hatching, although bioassays are required to give decisive answers about the mandibular gland's function.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00562.x" xmlns="http://purl.org/rss/1.0/"><title>An assessment approach for application of spermatic data in phylogenetic analyses: within the genus Moenkhausia Eigenmann, 1903 (Characiformes: Characidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00562.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">An assessment approach for application of spermatic data in phylogenetic analyses: within the genus Moenkhausia Eigenmann, 1903 (Characiformes: Characidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Júlio C. O. Santana, Clarianna M. Baicere-Silva, Priscila Gusmão-Pompiani, Ricardo C. Benine, Irani Quagio-Grassiotto</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-23T05:49:47.854726-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00562.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00562.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00562.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Spermiogenesis and sperm ultrastructure from 21 species of <em>Moenkhausia</em> and others related genera are described. To evaluate the phylogenetic signals, 18 unordered characters were utilized in implied weighting analysis through the program TNT 1.1. Four variations of spermiogenesis were found. In the earliest spermatids, the nucleus can be positioned lateral, eccentric, strongly eccentric or nearly medial in relation to the distal centriole. The nuclear rotation can be present or absent. These spermiogenesis processes are related or intermediate to Type I and Type III. Taking into account the degrees of nuclear rotation during the spermiogenesis and other characteristics, distinct forms of spermatozoa are observed among the species analyzed. The phylogenetic analysis yielded a single most parsimonious tree with fit value 2.70000 and the topology obtained founds <em>Moenkhausia</em> as non-monophyletic. However, some hypothesis of relationships previously proposed viz the clade 20, which contains the type species <em>Moenkhausia xinguensis</em>, is recovered herein. This clade is supported by five synapomorphies, and it allows the supposition that these species constitute a monophyletic group. The whole topology is presented and discussed.</p></div>]]></content:encoded><description>Spermiogenesis and sperm ultrastructure from 21 species of Moenkhausia and others related genera are described. To evaluate the phylogenetic signals, 18 unordered characters were utilized in implied weighting analysis through the program TNT 1.1. Four variations of spermiogenesis were found. In the earliest spermatids, the nucleus can be positioned lateral, eccentric, strongly eccentric or nearly medial in relation to the distal centriole. The nuclear rotation can be present or absent. These spermiogenesis processes are related or intermediate to Type I and Type III. Taking into account the degrees of nuclear rotation during the spermiogenesis and other characteristics, distinct forms of spermatozoa are observed among the species analyzed. The phylogenetic analysis yielded a single most parsimonious tree with fit value 2.70000 and the topology obtained founds Moenkhausia as non-monophyletic. However, some hypothesis of relationships previously proposed viz the clade 20, which contains the type species Moenkhausia xinguensis, is recovered herein. This clade is supported by five synapomorphies, and it allows the supposition that these species constitute a monophyletic group. The whole topology is presented and discussed.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00560.x" xmlns="http://purl.org/rss/1.0/"><title>Sexual dimorphisms in the dermal structure of the lesser-spotted catshark, Scyliorhinus canicula (Linnaeus, 1758)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00560.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sexual dimorphisms in the dermal structure of the lesser-spotted catshark, Scyliorhinus canicula (Linnaeus, 1758)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Neil Crooks, Colin P. Waring</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-25T01:38:50.086242-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2012.00560.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2012.00560.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2012.00560.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Sexual dimorphisms in the dermal structures of two elasmobranch species have previously been reported and it has been linked to the use of the mouth by males during copulation. Until relatively recently, the fact, that male <em>Scyliorhinus canicula</em> use their mouths for grasping and biting females during copulation was unknown. This study reveals that not only do adult (M ≥ 525 mm, F ≥ 550 mm) <em>S. canicula</em> show a sexual dimorphism in the epidermis and dermis, but that hatchling <em>S. canicula</em> are born with a sexually dimorphic epidermal layer and this persists into the juvenile stage (M &lt; 525 mm, F &lt; 550 mm). A sexual dimorphism was found in all size classes with both hatchling and juvenile female <em>S. canicula</em> having significantly thicker epidermal layers than hatchling and juvenile male <em>S. canicula</em>. Adult female <em>S. canicula</em> were found to possess both a significantly thicker epidermal and dermal layer than adult male <em>S. canicula</em>. The presence of a sexual dimorphism in the epidermal and dermal layers of adult <em>S. canicula</em> could be directly related to reproductive behaviour in response to the male biting the female prior to copulation.</p></div>]]></content:encoded><description>Sexual dimorphisms in the dermal structures of two elasmobranch species have previously been reported and it has been linked to the use of the mouth by males during copulation. Until relatively recently, the fact, that male Scyliorhinus canicula use their mouths for grasping and biting females during copulation was unknown. This study reveals that not only do adult (M ≥ 525 mm, F ≥ 550 mm) S. canicula show a sexual dimorphism in the epidermis and dermis, but that hatchling S. canicula are born with a sexually dimorphic epidermal layer and this persists into the juvenile stage (M &lt; 525 mm, F &lt; 550 mm). A sexual dimorphism was found in all size classes with both hatchling and juvenile female S. canicula having significantly thicker epidermal layers than hatchling and juvenile male S. canicula. Adult female S. canicula were found to possess both a significantly thicker epidermal and dermal layer than adult male S. canicula. The presence of a sexual dimorphism in the epidermal and dermal layers of adult S. canicula could be directly related to reproductive behaviour in response to the male biting the female prior to copulation.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00557.x" xmlns="http://purl.org/rss/1.0/"><title>The complete larval development of Panopeus lacustris Desbonne 1867 (Brachyura: Panopeidae), from the Amazon region, reared in the laboratory</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00557.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The complete larval development of Panopeus lacustris Desbonne 1867 (Brachyura: Panopeidae), from the Amazon region, reared in the laboratory</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adelson S. de Souza, Rauquírio M. da Costa, Fernando A. Abrunhosa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-25T01:32:31.182535-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00557.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00557.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00557.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>de Souza, A.S., da Costa R.M. and Abrunhosa F.A. 2011. The complete larval development of <em>Panopeus lacustris</em> Desbonne 1867 (Brachyura: Panopeidae), from the Amazon region, reared in the laboratory. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–16.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Larvae of the mud crab <em>Panopeus lacustris</em> were reared in laboratory from ovigerous females collected in the estuarine area of the Caeté River in the Amazonian region. The complete development of this species consisted of four zoeal and one megalopal stages, which were described and illustrated in detail. The results are compared with those of other previous studies on larval development of the species belonging to the genus <em>Panopeus</em> and then briefly discussed.</p></div>]]></content:encoded><description>de Souza, A.S., da Costa R.M. and Abrunhosa F.A. 2011. The complete larval development of Panopeus lacustris Desbonne 1867 (Brachyura: Panopeidae), from the Amazon region, reared in the laboratory. —Acta Zoologica (Stockholm) 00: 1–16.Larvae of the mud crab Panopeus lacustris were reared in laboratory from ovigerous females collected in the estuarine area of the Caeté River in the Amazonian region. The complete development of this species consisted of four zoeal and one megalopal stages, which were described and illustrated in detail. The results are compared with those of other previous studies on larval development of the species belonging to the genus Panopeus and then briefly discussed.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00558.x" xmlns="http://purl.org/rss/1.0/"><title>Sensilla on maxillary and labial palps in a helicophagous ground beetle larva (Coleoptera, Carabidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00558.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sensilla on maxillary and labial palps in a helicophagous ground beetle larva (Coleoptera, Carabidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anita Giglio, Enrico Perrotta, Federica Talarico, Tullia Zetto Brandmayr, Enrico A. Ferrero</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-18T02:11:03.275843-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00558.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00558.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00558.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Giglio, A., Perrotta, E., Talarico, F., Zetto Brandmayr, T. and Ferrero, E.A. 2011. Sensilla on maxillary and labial palps in a helicophagous ground beetle larva (Coleoptera, Carabidae). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–8.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Sensilla on the labial and maxillary palp of <em>Carabus lefebvrei</em> Dejean, 1826 larvae were investigated using scanning and transmission electron microscopy. Two identical sets of sensilla were present on the tips of both palp pairs, and four morphological types of sensilla were identified: sensilla basiconica types 1 and 2, sensilla coeloconica and sensilla digitiformia. Ultrastructure indicates that the sensilla basiconica type 1 and coeloconica have a chemical role as gustatory and olfactory receptors, respectively, while sensilla basiconica type 2 are mechanoreceptors and the sensilla digitiformia are probably thermo- and hygroreceptors. Their function is discussed in relation to specialized prey detection and habitat adaptations.</p></div>]]></content:encoded><description>Giglio, A., Perrotta, E., Talarico, F., Zetto Brandmayr, T. and Ferrero, E.A. 2011. Sensilla on maxillary and labial palps in a helicophagous ground beetle larva (Coleoptera, Carabidae). —Acta Zoologica (Stockholm) 00: 1–8.Sensilla on the labial and maxillary palp of Carabus lefebvrei Dejean, 1826 larvae were investigated using scanning and transmission electron microscopy. Two identical sets of sensilla were present on the tips of both palp pairs, and four morphological types of sensilla were identified: sensilla basiconica types 1 and 2, sensilla coeloconica and sensilla digitiformia. Ultrastructure indicates that the sensilla basiconica type 1 and coeloconica have a chemical role as gustatory and olfactory receptors, respectively, while sensilla basiconica type 2 are mechanoreceptors and the sensilla digitiformia are probably thermo- and hygroreceptors. Their function is discussed in relation to specialized prey detection and habitat adaptations.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00556.x" xmlns="http://purl.org/rss/1.0/"><title>Morphology of the female genital ducts of the blue land crab Cardisoma guanhumi (Crustacea: Brachyura: Gecarcinidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00556.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Morphology of the female genital ducts of the blue land crab Cardisoma guanhumi (Crustacea: Brachyura: Gecarcinidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leonardo P. de Souza, José R.F. Silva, Andréa M. Araujo, Maria I. Camargo-Mathias</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-06T07:44:45.298931-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00556.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00556.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00556.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>de Souza. L.P., Silva, J.R.F., Araujo, A.M. and Camargo-Mathias M.I. (2011). Morphology of the female genital ducts of the blue land crab <em>Cardisoma guanhumi</em> (Crustacea: Brachyura: Gecarcinidae). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–8.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This is a histological and histochemical analysis of the terminal portion of the female reproductive system and genital ducts of the blue land crab (<em>Cardisoma guanhumi</em>). Animals were collected in the Jaguaribe estuary (Ceará, Brazil) and dissected. Genital duct fragments were fixed and submitted to different staining techniques. The female reproductive system consists of a pair of ovaries and a pair of genital ducts. In the mid-posterior portion of each lobe, the ovaries communicate with the genital ducts, which are subdivided into oviduct, spermatheca, vagina, and gonopore. Histologically, the spermatheca of <em>C. guanhumi</em> is composed of columnar secretory epithelium and is divided into a dorsal zone and a ventral zone, the latter covered internally by a cuticle layer. Both zones are enveloped by a thin layer of loose connective tissue. Histological cross sections revealed the vagina to be concave, a pattern considered phylogenetically more advanced than the simple, tubular form. Our findings suggest fertilization is internal, favoring sperm from the most recent copulation.</p></div>]]></content:encoded><description>de Souza. L.P., Silva, J.R.F., Araujo, A.M. and Camargo-Mathias M.I. (2011). Morphology of the female genital ducts of the blue land crab Cardisoma guanhumi (Crustacea: Brachyura: Gecarcinidae). —Acta Zoologica (Stockholm) 00: 1–8.This is a histological and histochemical analysis of the terminal portion of the female reproductive system and genital ducts of the blue land crab (Cardisoma guanhumi). Animals were collected in the Jaguaribe estuary (Ceará, Brazil) and dissected. Genital duct fragments were fixed and submitted to different staining techniques. The female reproductive system consists of a pair of ovaries and a pair of genital ducts. In the mid-posterior portion of each lobe, the ovaries communicate with the genital ducts, which are subdivided into oviduct, spermatheca, vagina, and gonopore. Histologically, the spermatheca of C. guanhumi is composed of columnar secretory epithelium and is divided into a dorsal zone and a ventral zone, the latter covered internally by a cuticle layer. Both zones are enveloped by a thin layer of loose connective tissue. Histological cross sections revealed the vagina to be concave, a pattern considered phylogenetically more advanced than the simple, tubular form. Our findings suggest fertilization is internal, favoring sperm from the most recent copulation.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00555.x" xmlns="http://purl.org/rss/1.0/"><title>Ovarian maturation and oogenesis in the blue swimmer crab, Portunus pelagicus (Decapoda: Portunidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00555.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ovarian maturation and oogenesis in the blue swimmer crab, Portunus pelagicus (Decapoda: Portunidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Raghunath Ravi, Mary K. Manisseri, Nandiath Karayi Sanil</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-06T06:23:41.647215-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00555.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00555.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00555.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Ravi, R., Manisseri, M.K. and K.S., N. 2011. Ovarian maturation and oogenesis in the blue swimmer crab, <em>Portunus pelagicus</em> (Decapoda: Portunidae). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–9.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The study was aimed at understanding the process of reproduction and the changes happening in the ovary of <em>Portunus pelagicus</em> during maturation, which would be useful for its broodstock development for hatchery purposes. For that, tissue samples from different regions of the ovary at various stages of maturation were subjected to light and electron microscopy, and based on the changes revealed and the differences in ovarian morphology, the ovary was divided into five stages such as immature (previtellogenic oocytes), early maturing (early vitellogenic oocytes), late maturing (late vitellogenic oocytes), mature (vitellogenic oocytes), and spent (resorbing oocytes). The ovarian wall comprised of an outermost thin pavement epithelium, a middle layer of connective tissue, and an innermost layer of germinal epithelium. The oocytes matured as they moved from the centrally placed germinal zone toward the ovarian wall. The peripheral arrangement of nucleolar materials and the high incidence of cell organelles during the initial stages indicated vitellogenesis I. Movement of follicle cells toward oocytes in the early maturing stage and low incidence of mitochondria and endoplasmic reticulum in the ooplasm during late vitellogenic stage marked the commencement and end of vitellogenesis II, respectively. Yolk granules at various stages of development were seen in the ooplasm from late vitellogenic stage onwards. The spent ovary had an area with resorbing oocytes and empty follicle cells denoting the end of one reproductive cycle and another area with oogonial cells and previtellogenic oocytes indicating the beginning of the next.</p></div>]]></content:encoded><description>Ravi, R., Manisseri, M.K. and K.S., N. 2011. Ovarian maturation and oogenesis in the blue swimmer crab, Portunus pelagicus (Decapoda: Portunidae). —Acta Zoologica (Stockholm) 00: 1–9.The study was aimed at understanding the process of reproduction and the changes happening in the ovary of Portunus pelagicus during maturation, which would be useful for its broodstock development for hatchery purposes. For that, tissue samples from different regions of the ovary at various stages of maturation were subjected to light and electron microscopy, and based on the changes revealed and the differences in ovarian morphology, the ovary was divided into five stages such as immature (previtellogenic oocytes), early maturing (early vitellogenic oocytes), late maturing (late vitellogenic oocytes), mature (vitellogenic oocytes), and spent (resorbing oocytes). The ovarian wall comprised of an outermost thin pavement epithelium, a middle layer of connective tissue, and an innermost layer of germinal epithelium. The oocytes matured as they moved from the centrally placed germinal zone toward the ovarian wall. The peripheral arrangement of nucleolar materials and the high incidence of cell organelles during the initial stages indicated vitellogenesis I. Movement of follicle cells toward oocytes in the early maturing stage and low incidence of mitochondria and endoplasmic reticulum in the ooplasm during late vitellogenic stage marked the commencement and end of vitellogenesis II, respectively. Yolk granules at various stages of development were seen in the ooplasm from late vitellogenic stage onwards. The spent ovary had an area with resorbing oocytes and empty follicle cells denoting the end of one reproductive cycle and another area with oogonial cells and previtellogenic oocytes indicating the beginning of the next.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00553.x" xmlns="http://purl.org/rss/1.0/"><title>Genital morphology of female goblin spiders (Arachnida: Araneae: Oonopidae) with functional implications</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00553.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genital morphology of female goblin spiders (Arachnida: Araneae: Oonopidae) with functional implications</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Matthias Burger</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-19T01:41:04.254033-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00553.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00553.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00553.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Burger, M. 2011. Genital morphology of female goblin spiders (Arachnida: Araneae: Oonopidae) with functional implications. —<em>Acta Zoologica</em> (Stockholm) <b>00:</b> 1–11.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Spider genital morphology usually provides the best characters for taxonomy. Furthermore, functional genital morphology helps to understand the evolution of complex genitalia and their role in the context of sexual selection. The genital systems of most haplogyne spider families are poorly investigated with respect to their morphology. The present study investigates the female genitalia of the oonopids <em>Oonops pulcher</em>, <em>Oonopinus kilikus</em>, and <em>Pseudotriaeris</em> sp. by means of light microscopy and SEM. The male palps are briefly described. Females of <em>O. pulcher</em> store spermatozoa in an anterior and a posterior receptaculum (PRe). The genitalia resemble the primitive dysderoid genitalia supporting the hypothesis that the subfamily Oonopinae contains more basal oonopids. In <em>O. kilikus,</em> the anterior receptaculum is reduced to a sclerite. Spermatozoa are stored in a PRe. The receptacula of <em>Pseudotriaeris</em> sp. are reduced to sclerites. Spermatozoa in the uterus internus indicate that fertilization happens there or in the ovary. The anterior sclerite might serve females to lock the uterus during copulation as suggested for other gamasomorphines. The male palp of <em>O. kilikus</em> is simple, whereas the palps of <em>O. pulcher</em> and <em>Pseudotriaeris</em> sp. appear more complex. Complicated structures on the palp of <em>Pseudotriaeris</em> sp. indicate that males exert copulatory courtship.</p></div>]]></content:encoded><description>Burger, M. 2011. Genital morphology of female goblin spiders (Arachnida: Araneae: Oonopidae) with functional implications. —Acta Zoologica (Stockholm) 00: 1–11.Spider genital morphology usually provides the best characters for taxonomy. Furthermore, functional genital morphology helps to understand the evolution of complex genitalia and their role in the context of sexual selection. The genital systems of most haplogyne spider families are poorly investigated with respect to their morphology. The present study investigates the female genitalia of the oonopids Oonops pulcher, Oonopinus kilikus, and Pseudotriaeris sp. by means of light microscopy and SEM. The male palps are briefly described. Females of O. pulcher store spermatozoa in an anterior and a posterior receptaculum (PRe). The genitalia resemble the primitive dysderoid genitalia supporting the hypothesis that the subfamily Oonopinae contains more basal oonopids. In O. kilikus, the anterior receptaculum is reduced to a sclerite. Spermatozoa are stored in a PRe. The receptacula of Pseudotriaeris sp. are reduced to sclerites. Spermatozoa in the uterus internus indicate that fertilization happens there or in the ovary. The anterior sclerite might serve females to lock the uterus during copulation as suggested for other gamasomorphines. The male palp of O. kilikus is simple, whereas the palps of O. pulcher and Pseudotriaeris sp. appear more complex. Complicated structures on the palp of Pseudotriaeris sp. indicate that males exert copulatory courtship.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00552.x" xmlns="http://purl.org/rss/1.0/"><title>Autophagy as the cell survival in response to a microsporidian infection of the midgut epithelium of Isohypsibius granulifer granulifer (Eutardigrada: Hypsibiidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00552.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Autophagy as the cell survival in response to a microsporidian infection of the midgut epithelium of Isohypsibius granulifer granulifer (Eutardigrada: Hypsibiidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Magdalena M. Rost-Roszkowska, Izabela Poprawa, Łukasz Kaczmarek</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-19T01:40:55.398453-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00552.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00552.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00552.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Rost-Roszkowska, M.M., Poprawa, I., Kaczmarek, Ł. 2011. Autophagy as the cell survival in response to a microsporidian infection of the midgut epithelium of <em>Isohypsibius granulifer granulifer</em> (Eutardigrada: Hypsibiidae). —<em>Acta Zoologica</em> (Stockholm) <b>00:</b> 1–7.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The midgut epithelial cells of many invertebrates may possess microorganisms which act as symbionts or pathogens (bacteria, microsporidia, viruses). During our previous studies on <em>Isohypsibius granulifer granulifer</em> Thulin, 1928 (Tardigrada, Eutardigrada), which examined alterations of the midgut epithelium during oogenesis, we found that some of the specimens were infected with microsporidia. All stages of pathogens occurred in the cytoplasm of the digestive cells in the midgut epithelium of <em>I. g. granulifer</em> that were infected with microsporidia: meronts, sporonts, sporoblasts, and spores. The cytoplasm of the digestive cells was rich in mitochondria, cisterns of rough endoplasmic reticulum (RER), and Golgi complexes. Autophagy in the digestive cells of the dorsal midgut was much more intensive in comparison with noninfected specimens. Membranes of phagophores surrounded the pathogens forming autophagosomes. These latter structures fused with lysosomes forming autolysosomes and residual bodies appeared. Neither glycogen granules nor droplets of varying electron density, which accumulated in digestive cells during vitellogenesis and choriogenesis, appeared in individuals with microsporidia. While the midgut epithelium in noninfected specimens takes part in vitellogenesis and choriogenesis, in infected specimens, midgut cells are involved in the process of autophagy as a survival strategy.</p></div>]]></content:encoded><description>Rost-Roszkowska, M.M., Poprawa, I., Kaczmarek, Ł. 2011. Autophagy as the cell survival in response to a microsporidian infection of the midgut epithelium of Isohypsibius granulifer granulifer (Eutardigrada: Hypsibiidae). —Acta Zoologica (Stockholm) 00: 1–7.The midgut epithelial cells of many invertebrates may possess microorganisms which act as symbionts or pathogens (bacteria, microsporidia, viruses). During our previous studies on Isohypsibius granulifer granulifer Thulin, 1928 (Tardigrada, Eutardigrada), which examined alterations of the midgut epithelium during oogenesis, we found that some of the specimens were infected with microsporidia. All stages of pathogens occurred in the cytoplasm of the digestive cells in the midgut epithelium of I. g. granulifer that were infected with microsporidia: meronts, sporonts, sporoblasts, and spores. The cytoplasm of the digestive cells was rich in mitochondria, cisterns of rough endoplasmic reticulum (RER), and Golgi complexes. Autophagy in the digestive cells of the dorsal midgut was much more intensive in comparison with noninfected specimens. Membranes of phagophores surrounded the pathogens forming autophagosomes. These latter structures fused with lysosomes forming autolysosomes and residual bodies appeared. Neither glycogen granules nor droplets of varying electron density, which accumulated in digestive cells during vitellogenesis and choriogenesis, appeared in individuals with microsporidia. While the midgut epithelium in noninfected specimens takes part in vitellogenesis and choriogenesis, in infected specimens, midgut cells are involved in the process of autophagy as a survival strategy.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00550.x" xmlns="http://purl.org/rss/1.0/"><title>Spermatophore formation and sperm ultrastructure of Sundathelphusa philippina (Crustacea: Brachyura: Gecarcinucidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00550.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Spermatophore formation and sperm ultrastructure of Sundathelphusa philippina (Crustacea: Brachyura: Gecarcinucidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sebastian Klaus, Susann Münzner, Anna-Christina Modenbach, Bruno Streit, Christopher C. Tudge</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-19T01:40:50.863155-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00550.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00550.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00550.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Klaus, S., Münzner, S., Modenbach, A.-C., Streit, B. and Tudge, C.C. (2011). Spermatophore formation and sperm ultrastructure of <em>Sundathelphusa philippina</em> (Crustacea: Brachyura: Gecarcinucidae). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–6.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We investigated the morphology of spermatozoa, spermatophores and the anterior vas deferens (AVD) of the gecarcinucid freshwater crab <em>Sundathelphusa philippina</em>. The morphology of the acrosome (proportions, structure and arrangement of acrosomal layers) and the spermatophores complies with the known sperm and spermatophore morphology of the brachyuran family Gecarcinucidae. The sperm cells are packed within coenospermic spermatophores that are of a mucous type, lacking a complex spermatophore wall. Spermatophore formation takes place in the distal part of the AVD. The strongly proliferated inner epithelium of the vas deferens releases vesicles via apocrine secretion. These vesicles fuse with the incipient spermatophores that subsequently coalesce, thus forming the coenospermic aggregates that represent the mature spermatophores.</p></div>]]></content:encoded><description>Klaus, S., Münzner, S., Modenbach, A.-C., Streit, B. and Tudge, C.C. (2011). Spermatophore formation and sperm ultrastructure of Sundathelphusa philippina (Crustacea: Brachyura: Gecarcinucidae). —Acta Zoologica (Stockholm) 00: 1–6.We investigated the morphology of spermatozoa, spermatophores and the anterior vas deferens (AVD) of the gecarcinucid freshwater crab Sundathelphusa philippina. The morphology of the acrosome (proportions, structure and arrangement of acrosomal layers) and the spermatophores complies with the known sperm and spermatophore morphology of the brachyuran family Gecarcinucidae. The sperm cells are packed within coenospermic spermatophores that are of a mucous type, lacking a complex spermatophore wall. Spermatophore formation takes place in the distal part of the AVD. The strongly proliferated inner epithelium of the vas deferens releases vesicles via apocrine secretion. These vesicles fuse with the incipient spermatophores that subsequently coalesce, thus forming the coenospermic aggregates that represent the mature spermatophores.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00541.x" xmlns="http://purl.org/rss/1.0/"><title>Chironomid midges: a forgotten model of developmental biology research</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00541.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Chironomid midges: a forgotten model of developmental biology research</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leena J. Thorat, Bimalendu B. Nath</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-14T21:47:44.334218-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00541.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00541.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00541.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">REVIEW ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>Thorat, L.J. and Nath, B.B. 2011. Chironomid midges: a forgotten model of developmental biology research. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–5.</p></div></div><div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h4>Abstract</h4><div class="para"><p>For more than a century, embryologists have been exploring various model systems to gain insights into developmental processes. This article presents an overview of the role of chironomid midges in embryology research since their introduction as model organisms in the 19th century. We present the vestiges of bibliography since the days of Weismann (1834–1914), who raised preliminary queries to unravel many unique features of insect embryogenesis using midges as a crucible. Unfortunately, over the years, chironomid midges got lost into obscurity as a model for developmental biology, which is evident from the paucity of developmental biology–related literature on midges in the past decades. Through this essay, the authors intend to share reminiscences of the heydays of chironomid research with the wider community of zoologists with an aim of reviving chironomid embryology. Midges not only possess the basic qualities essential for an ideal model system, but being one of the ancestral dipteran stocks, they can also prove an excellent test system for evo-devo, transgenetic, and embryogenomic investigations that utilize methodologies at the interface of developmental biology and high-throughput molecular genetic and genomics approach. An introspection of re-introducing chironomid midgesas model system will be rewarding for the contemporary developmental biologists.</p></div></div>]]></content:encoded><description>Thorat, L.J. and Nath, B.B. 2011. Chironomid midges: a forgotten model of developmental biology research. —Acta Zoologica (Stockholm) 00: 1–5.AbstractFor more than a century, embryologists have been exploring various model systems to gain insights into developmental processes. This article presents an overview of the role of chironomid midges in embryology research since their introduction as model organisms in the 19th century. We present the vestiges of bibliography since the days of Weismann (1834–1914), who raised preliminary queries to unravel many unique features of insect embryogenesis using midges as a crucible. Unfortunately, over the years, chironomid midges got lost into obscurity as a model for developmental biology, which is evident from the paucity of developmental biology–related literature on midges in the past decades. Through this essay, the authors intend to share reminiscences of the heydays of chironomid research with the wider community of zoologists with an aim of reviving chironomid embryology. Midges not only possess the basic qualities essential for an ideal model system, but being one of the ancestral dipteran stocks, they can also prove an excellent test system for evo-devo, transgenetic, and embryogenomic investigations that utilize methodologies at the interface of developmental biology and high-throughput molecular genetic and genomics approach. An introspection of re-introducing chironomid midgesas model system will be rewarding for the contemporary developmental biologists.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00539.x" xmlns="http://purl.org/rss/1.0/"><title>The contribution of developmental palaeontology to extensions of evolutionary theory</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00539.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The contribution of developmental palaeontology to extensions of evolutionary theory</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laura A. B. Wilson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-09T23:09:36.840563-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00539.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00539.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00539.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Wilson, L.A.B. 2011. The contribution of developmental palaeontology to extensions of evolutionary theory. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–7.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Evo-devo is featuring prominently in current discussion to extend evolutionary theory. Developmental palaeontology, the study of life history evolution and ontogeny in fossils, remains an area of investigation that could benefit from, but also illuminate, the discourse and research agenda of evo-devo. Understanding how and why evolution proceeds in phenotypic space is an important goal of evo-devo and one that can be significantly enriched through the examination of development in the fossil record (Palaeo-evo-devo). Such an approach permits developmental pathways to be extended into the past, constraining hypotheses of developmental evolution in ways that cannot be predicted by patterns observed from extant taxa alone. The comparison of developmental dynamics among extant and extinct taxa yields a more complete understanding of the temporal persistence of factors that shape evolution in phenotypic space. As more data are compiled that document ‘fossilized ontogenies’, a stage will emerge from which insights into the evolution of development can begin to appraise those phenotypes that are inaccessible to evo-devo.</p></div>]]></content:encoded><description>Wilson, L.A.B. 2011. The contribution of developmental palaeontology to extensions of evolutionary theory. —Acta Zoologica (Stockholm) 00: 1–7.Evo-devo is featuring prominently in current discussion to extend evolutionary theory. Developmental palaeontology, the study of life history evolution and ontogeny in fossils, remains an area of investigation that could benefit from, but also illuminate, the discourse and research agenda of evo-devo. Understanding how and why evolution proceeds in phenotypic space is an important goal of evo-devo and one that can be significantly enriched through the examination of development in the fossil record (Palaeo-evo-devo). Such an approach permits developmental pathways to be extended into the past, constraining hypotheses of developmental evolution in ways that cannot be predicted by patterns observed from extant taxa alone. The comparison of developmental dynamics among extant and extinct taxa yields a more complete understanding of the temporal persistence of factors that shape evolution in phenotypic space. As more data are compiled that document ‘fossilized ontogenies’, a stage will emerge from which insights into the evolution of development can begin to appraise those phenotypes that are inaccessible to evo-devo.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00533.x" xmlns="http://purl.org/rss/1.0/"><title>External eggshell morphology of Anastrepha fruit flies (Diptera: Tephritidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00533.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">External eggshell morphology of Anastrepha fruit flies (Diptera: Tephritidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Julia V. A. Figueiredo, André L. P. Perondini, Eliana M. Ruggiro, Leandro F. Prezotto, Denise Selivon</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-08T02:20:57.665451-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00533.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00533.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00533.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">REVIEW ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">125</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">133</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Figueiredo J.V.A., Perondini A.L.P., Ruggiro EM., Prezotto LF. and Selivon D. (2011). External eggshell morphology of <em>Anastrepha</em> fruit flies (Diptera: Tephritidae). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>:1–9.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The eggshell external morphology of <em>Anastrepha</em> species of different taxonomic intrageneric groups was determined by light and scanning electron microscopy. The eggs of <em>Anastrepha alveata</em> Stone and <em>A. consobrina</em> (Loew) are described for the first time, and a more detailed description of previously studied eggs from <em>A. amita</em> Zucchi, <em>A. pickeli</em> Lima, <em>A. bistrigata</em> Bezzi, <em>A. grandis</em> (Macquart), <em>A. obliqua</em> (Macquart), <em>A. pseudoparallela</em> (Loew), <em>A. striata</em> Schiner, <em>A. suspensa</em> (Loew), and <em>A. zenildae</em> Zucchi is presented. Several relatively plastic morphological characters of the eggs were discerned, such as length, width, tapering, curvature, chorion ornamentation, respiratory lobes, and position of the micropyle. Scores were attributed to these characters, allowing a comparison of egg morphology among 17 species of <em>Anastrepha</em>. A cluster analysis based on these scores did not group the eggs according to the taxonomic intrageneric groups of the species. Nonetheless, this analysis indicated that the egg of each species can be described by a set of morphological scores. The possibility of species identificaton using immature stages will be of great help for the taxonomy of <em>Anastrepha</em> fruit flies.</p></div>
]]></content:encoded><description>

Figueiredo J.V.A., Perondini A.L.P., Ruggiro EM., Prezotto LF. and Selivon D. (2011). External eggshell morphology of Anastrepha fruit flies (Diptera: Tephritidae). —Acta Zoologica (Stockholm) 00:1–9.
The eggshell external morphology of Anastrepha species of different taxonomic intrageneric groups was determined by light and scanning electron microscopy. The eggs of Anastrepha alveata Stone and A. consobrina (Loew) are described for the first time, and a more detailed description of previously studied eggs from A. amita Zucchi, A. pickeli Lima, A. bistrigata Bezzi, A. grandis (Macquart), A. obliqua (Macquart), A. pseudoparallela (Loew), A. striata Schiner, A. suspensa (Loew), and A. zenildae Zucchi is presented. Several relatively plastic morphological characters of the eggs were discerned, such as length, width, tapering, curvature, chorion ornamentation, respiratory lobes, and position of the micropyle. Scores were attributed to these characters, allowing a comparison of egg morphology among 17 species of Anastrepha. A cluster analysis based on these scores did not group the eggs according to the taxonomic intrageneric groups of the species. Nonetheless, this analysis indicated that the egg of each species can be described by a set of morphological scores. The possibility of species identificaton using immature stages will be of great help for the taxonomy of Anastrepha fruit flies.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00537.x" xmlns="http://purl.org/rss/1.0/"><title>The ovarian cycle histochemistry and its relationship with hepatopancreas weight in the blue crab Callinectes danae (Crustacea: Portunidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00537.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The ovarian cycle histochemistry and its relationship with hepatopancreas weight in the blue crab Callinectes danae (Crustacea: Portunidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fernando J. Zara, Henrique H. Gaeta, Tânia M. Costa, Marcos H. Toyama, Flávio H. Caetano</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-17T23:27:33.817756-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00537.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00537.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00537.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">REVIEW ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">134</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">146</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Zara, F.J., Gaeta, H.H., Costa, T.M., Toyama, M.H. and Caetano, F.H. 2011. The ovarian cycle histochemistry and its relationship with hepatopancreas weight in the blue crab <em>Callinectes danae</em> (Crustacea: Portunidae). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>:1–13.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Several studies use macroscopic patterns of the ovarian development in crustaceans. Here, we examined the relationship between ovary histochemistry, changes in gonadosomatic and hepatosomatic indices against the macroscopic pattern of the ovarian development in <em>Callinectes danae</em>. Animals were collected in the south coast of São Paulo State, Brazil. Ovaries were macroscopically classified as juvenile, rudimentary, developing, intermediary, mature, and rudimentary ovigerous. Samples were fixed in 4% paraformaldehyde, processed for historesin, and stained with HE, protein, and neutral and acid polysaccharides detection. The juvenile oocytes are not enclosed by follicular cells and have fewer yolk nuclei being less intense in PAS reactivity than rudimentary oocytes. Developing oocytes show yolk granules and thick follicular cells. Yolk granules were positive for proteins and neutral polysaccharides. The intermediary stage is marked by a qualitative increase in yolk granules and the onset of chorion formation. In mature oocytes, cytoplasm is completely filled by yolk granules and the chorion is completely formed. Ovigerous ovaries have several atretic follicles and large quantities of hemocytes in the process of tissue reorganization. In <em>C. danae,</em> the changes in cell, goandosomatic and hepatosomatic indices coinciding with macroscopic observations and any combination of different macroscopic stages in a single pattern should be avoided.</p></div>
]]></content:encoded><description>

Zara, F.J., Gaeta, H.H., Costa, T.M., Toyama, M.H. and Caetano, F.H. 2011. The ovarian cycle histochemistry and its relationship with hepatopancreas weight in the blue crab Callinectes danae (Crustacea: Portunidae). —Acta Zoologica (Stockholm) 00:1–13.
Several studies use macroscopic patterns of the ovarian development in crustaceans. Here, we examined the relationship between ovary histochemistry, changes in gonadosomatic and hepatosomatic indices against the macroscopic pattern of the ovarian development in Callinectes danae. Animals were collected in the south coast of São Paulo State, Brazil. Ovaries were macroscopically classified as juvenile, rudimentary, developing, intermediary, mature, and rudimentary ovigerous. Samples were fixed in 4% paraformaldehyde, processed for historesin, and stained with HE, protein, and neutral and acid polysaccharides detection. The juvenile oocytes are not enclosed by follicular cells and have fewer yolk nuclei being less intense in PAS reactivity than rudimentary oocytes. Developing oocytes show yolk granules and thick follicular cells. Yolk granules were positive for proteins and neutral polysaccharides. The intermediary stage is marked by a qualitative increase in yolk granules and the onset of chorion formation. In mature oocytes, cytoplasm is completely filled by yolk granules and the chorion is completely formed. Ovigerous ovaries have several atretic follicles and large quantities of hemocytes in the process of tissue reorganization. In C. danae, the changes in cell, goandosomatic and hepatosomatic indices coinciding with macroscopic observations and any combination of different macroscopic stages in a single pattern should be avoided.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00547.x" xmlns="http://purl.org/rss/1.0/"><title>Microstructural morphology in early dermal denticles of hammerhead sharks (Elasmobranchii: Sphyrnidae) and related taxa</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00547.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Microstructural morphology in early dermal denticles of hammerhead sharks (Elasmobranchii: Sphyrnidae) and related taxa</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Waldiney C. Mello, Jorge J. de Carvalho, Paulo M. M. Brito</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-21T05:53:49.251341-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00547.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00547.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00547.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">REVIEW ARTICLE</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">147</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">153</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Mello, W.C., de Carvalho, J.J., Brito, P.M.M. 2011. Microstructural morphology in early dermal denticles of hammerhead sharks (Elasmobranchii: Sphyrnidae) and related taxa. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–7.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study uses scanning electron microscopies to investigate and describe the microstructural diversity of dermal denticles in the family Sphyrnidae, which comprises all living hammerhead shark species, comparing them to other related taxa (i.e. <em>Carcharhinus dussumieri</em>, <em>Carcharhinus plumbeus</em>, <em>Carcharhinus acronotus</em>, <em>Rhizoprionodon acutus</em>, <em>Negaprion brevirostris</em> and <em>Hemigaleus microstoma</em>). The results reveal that sphyrnids present noticeable microstructures in the dermal denticles, distinguishing them from the other related species investigated. Additionally, scale patterns are the same in three distinct body regions (i.e. cephalic, branchial and dorsal fin). Species of Sphyrnidae that reach bigger total lengths and that are widely distributed (i.e. <em>Sphyrna lewini</em> and <em>Sphyrna mokarran</em>) presented more, smaller and nearly hexagonal microstructures that do not cover the entire scale surface, unlike species reaching smaller sizes and restricted to coastal habits (i.e. <em>Sphyrna tiburo</em>, <em>Sphyrna tudes</em>, <em>Sphyrna media</em> and <em>Eusphyra blochii</em>). The sphyrnid scales are similar to <em>R. acutus</em> and <em>C. dussumieri</em> rather than to the other species, but it is not possible to identify the sphyrnid species only by scale features. It is clear that a similar morphology of scales is not necessarily related to similar life habits, and that they are candidates to provide new characters in phylogenetical studies among sphyrnids.</p></div>
]]></content:encoded><description>

Mello, W.C., de Carvalho, J.J., Brito, P.M.M. 2011. Microstructural morphology in early dermal denticles of hammerhead sharks (Elasmobranchii: Sphyrnidae) and related taxa. —Acta Zoologica (Stockholm) 00: 1–7.
This study uses scanning electron microscopies to investigate and describe the microstructural diversity of dermal denticles in the family Sphyrnidae, which comprises all living hammerhead shark species, comparing them to other related taxa (i.e. Carcharhinus dussumieri, Carcharhinus plumbeus, Carcharhinus acronotus, Rhizoprionodon acutus, Negaprion brevirostris and Hemigaleus microstoma). The results reveal that sphyrnids present noticeable microstructures in the dermal denticles, distinguishing them from the other related species investigated. Additionally, scale patterns are the same in three distinct body regions (i.e. cephalic, branchial and dorsal fin). Species of Sphyrnidae that reach bigger total lengths and that are widely distributed (i.e. Sphyrna lewini and Sphyrna mokarran) presented more, smaller and nearly hexagonal microstructures that do not cover the entire scale surface, unlike species reaching smaller sizes and restricted to coastal habits (i.e. Sphyrna tiburo, Sphyrna tudes, Sphyrna media and Eusphyra blochii). The sphyrnid scales are similar to R. acutus and C. dussumieri rather than to the other species, but it is not possible to identify the sphyrnid species only by scale features. It is clear that a similar morphology of scales is not necessarily related to similar life habits, and that they are candidates to provide new characters in phylogenetical studies among sphyrnids.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00534.x" xmlns="http://purl.org/rss/1.0/"><title>Types and development pathways of lateral line scales in some teleost species</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00534.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Types and development pathways of lateral line scales in some teleost species</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Elena P. Voronina, Dianne R. Hughes</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-08T02:21:07.63045-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00534.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00534.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00534.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">154</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">166</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Voronina, E.P. and Hughes, D.R. 2011. Types and development pathways of lateral line scales in some teleost species. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–13.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A comparative study of lateral line scales (<em>lls</em>) in nine teleost species was undertaken to trace their ontogenetic structural changes. Three universal characters were used to describe and classify definitive and developing <em>lls</em>. The four main structural types in teleosts are represented. In adult fish, <em>lls</em> are the same structural type in all parts of lateral line in any one specimen, but number of tubules and their orientation may vary. In juvenile fish, except for one species, the structural type of every <em>lls</em> changes with growth, and this process progresses along the lateral line in the direction of development typical for the species. Definitive structural type of the <em>lls</em> is not determined by common scale type and size, presence or absence of nerve foramen on <em>lls</em>, scale overlapping or time of initiation of scales and trunk canal. Development pathways are proposed in which terminal states correspond to the final development of the most complex <em>lls</em> type in <em>Cyprinus carpio</em>, <em>Carassius carassius</em>, <em>Oncorhynchus mykiss</em>, <em>Diplodus annularis</em> and <em>Mullus barbatus</em>. The intermediate states of these pathways correspond to other types of <em>lls</em> as examples of pedomorphosis in <em>Perca fluviatilis</em>, <em>Sander lucioperca</em>, <em>Symphysodon aequifasciatus</em> and <em>Hippoglossoides platessoides</em>.</p></div>
]]></content:encoded><description>

Voronina, E.P. and Hughes, D.R. 2011. Types and development pathways of lateral line scales in some teleost species. —Acta Zoologica (Stockholm) 00: 1–13.
A comparative study of lateral line scales (lls) in nine teleost species was undertaken to trace their ontogenetic structural changes. Three universal characters were used to describe and classify definitive and developing lls. The four main structural types in teleosts are represented. In adult fish, lls are the same structural type in all parts of lateral line in any one specimen, but number of tubules and their orientation may vary. In juvenile fish, except for one species, the structural type of every lls changes with growth, and this process progresses along the lateral line in the direction of development typical for the species. Definitive structural type of the lls is not determined by common scale type and size, presence or absence of nerve foramen on lls, scale overlapping or time of initiation of scales and trunk canal. Development pathways are proposed in which terminal states correspond to the final development of the most complex lls type in Cyprinus carpio, Carassius carassius, Oncorhynchus mykiss, Diplodus annularis and Mullus barbatus. The intermediate states of these pathways correspond to other types of lls as examples of pedomorphosis in Perca fluviatilis, Sander lucioperca, Symphysodon aequifasciatus and Hippoglossoides platessoides.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00535.x" xmlns="http://purl.org/rss/1.0/"><title>Epibionts on the krill (Euphausia pacifica) from the E coast of Japan</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00535.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Epibionts on the krill (Euphausia pacifica) from the E coast of Japan</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gregorio Fernandez-Leborans</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-08T02:21:12.628051-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00535.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00535.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00535.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">167</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">176</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Fernandez-Leborans, G. 2011. Epibionts on the krill (<em>Euphausia pacifica</em>) from the E coast of Japan. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–10.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Specimens of <em>Euphausia pacifica</em> collected from shallow waters of the E coast of Japan showed ciliate epibionts belonging to two suctorian species: <em>Ephelota plana</em> and <em>Gymnodinioides</em> sp. The epibionts were present in a total of 27 anatomical units of <em>E. pacifica</em>, in numbers fluctuating between 8 and 80 individuals per basibiont. <em>Gymnodinioides</em> showed the highest mean number of epibionts. The presence–absence of epibionts indicated some specificity of the species by different locations on the basibiont body, which is corroborated by the analysis of the colonization throughout the longitudinal axis of the basibiont. <em>Ephelota plana</em> was recorded by the first time on <em>E. pacifica</em>, while <em>Gymnodinioides</em> sp. extended its geographical area with respect to previous studies. Morphological, taxonomical features of the species and the statistical analysis of their spatial distribution on <em>E. pacifica</em> are included.</p></div>
]]></content:encoded><description>

Fernandez-Leborans, G. 2011. Epibionts on the krill (Euphausia pacifica) from the E coast of Japan. —Acta Zoologica (Stockholm) 00: 1–10.
Specimens of Euphausia pacifica collected from shallow waters of the E coast of Japan showed ciliate epibionts belonging to two suctorian species: Ephelota plana and Gymnodinioides sp. The epibionts were present in a total of 27 anatomical units of E. pacifica, in numbers fluctuating between 8 and 80 individuals per basibiont. Gymnodinioides showed the highest mean number of epibionts. The presence–absence of epibionts indicated some specificity of the species by different locations on the basibiont body, which is corroborated by the analysis of the colonization throughout the longitudinal axis of the basibiont. Ephelota plana was recorded by the first time on E. pacifica, while Gymnodinioides sp. extended its geographical area with respect to previous studies. Morphological, taxonomical features of the species and the statistical analysis of their spatial distribution on E. pacifica are included.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00536.x" xmlns="http://purl.org/rss/1.0/"><title>Environmental condition related reproductive strategies and sex ratio in hydras</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00536.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Environmental condition related reproductive strategies and sex ratio in hydras</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anita Kaliszewicz, Agnieszka Lipińska</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-07T22:05:44.571546-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00536.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00536.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00536.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">177</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">183</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Kaliszewicz, A. and Lipińska, A. 2011. Environmental condition related reproductive strategies and sex ratio in hydras. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>:1–7.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Temperature and food supply appeared to affect sex ratio, sex composition and percentage of sexual individuals in three <em>Hydra</em> species: <em>Hydra vulgaris</em>, <em>Hydra circumcincta</em> and <em>Hydra viridissima</em>. We found three sexes present: females, males and hermaphrodites depending on environmental conditions. <em>Hydra vulgaris</em> appeared to be a species with a temperature-dependent sex determination (TSD). The males and hermaphrodites were present only under rising temperatures, whereas females were observed exclusively at lowering temperatures. Hydras reproduced asexually at constant room temperature. Unlimited food affected sex ratios and induced the presence of males in <em>H. circumcincta</em> at lowering temperatures. Thus, <em>H. circumcincta</em> may be recognised as another <em>Hydra</em> species in which sex is determined by environmental factors (ESD). Under rising temperatures, the number of hermaphroditic individuals was higher when food supply was unlimited in all three species, indicating that hermaphrodites may need more energy to produce both male and female gonads. Both temperature changes and food supply positively affected asexual reproductive strategies in hydras, especially budding rates. <em>Hydra circumcincta</em> appeared to be less agile than other hydras and able to self-fertilise. It is likely that self-fertilisation is an adaptation to the low probability of meeting a mate belonging to the other clone.</p></div>
]]></content:encoded><description>

Kaliszewicz, A. and Lipińska, A. 2011. Environmental condition related reproductive strategies and sex ratio in hydras. —Acta Zoologica (Stockholm) 00:1–7.
Temperature and food supply appeared to affect sex ratio, sex composition and percentage of sexual individuals in three Hydra species: Hydra vulgaris, Hydra circumcincta and Hydra viridissima. We found three sexes present: females, males and hermaphrodites depending on environmental conditions. Hydra vulgaris appeared to be a species with a temperature-dependent sex determination (TSD). The males and hermaphrodites were present only under rising temperatures, whereas females were observed exclusively at lowering temperatures. Hydras reproduced asexually at constant room temperature. Unlimited food affected sex ratios and induced the presence of males in H. circumcincta at lowering temperatures. Thus, H. circumcincta may be recognised as another Hydra species in which sex is determined by environmental factors (ESD). Under rising temperatures, the number of hermaphroditic individuals was higher when food supply was unlimited in all three species, indicating that hermaphrodites may need more energy to produce both male and female gonads. Both temperature changes and food supply positively affected asexual reproductive strategies in hydras, especially budding rates. Hydra circumcincta appeared to be less agile than other hydras and able to self-fertilise. It is likely that self-fertilisation is an adaptation to the low probability of meeting a mate belonging to the other clone.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00538.x" xmlns="http://purl.org/rss/1.0/"><title>Ovary structure and transovarial transmission of endosymbiotic microorganisms in Marchalina hellenica (Insecta, Hemiptera, Coccomorpha: Marchalinidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00538.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ovary structure and transovarial transmission of endosymbiotic microorganisms in Marchalina hellenica (Insecta, Hemiptera, Coccomorpha: Marchalinidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Teresa Szklarzewicz, Malgorzata Kalandyk-Kolodziejczyk, Marta Kot, Anna Michalik</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-17T23:27:40.125146-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00538.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00538.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00538.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">184</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">192</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Szklarzewicz, T., Kalandyk-Kolodziejczyk, M., Kot, M. and Michalik, A. 2011. Ovary structure and transovarial transmission of endosymbiotic microorganisms in <em>Marchalina hellenica</em> (Insecta, Hemiptera, Coccomorpha: Marchalinidae). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>:1–9.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The paired ovaries of <em>Marchalina hellenica</em> are composed of about 200 ovarioles of telotrophic type. In each ovariole, a trophic chamber, vitellarium and ovariolar stalk can be distinguished. The tropharia comprise trophocytes and early previtellogenic oocytes (termed arrested oocytes) or trophocytes only. The arrested oocytes are not capable of further development. In the vitellaria, single oocytes develop that are connected to the tropharium by means of broad nutritive cords. The number of germ cells (trophocytes and oocytes) constituting ovarioles is not constant and may range between 25 and 32. Numerous endosymbiotic bacteria occur in the cytoplasm of trophocytes. The endosymbionts are transported via nutritive cords to the developing oocyte. The obtained results are discussed in a phylogenetic context.</p></div>
]]></content:encoded><description>

Szklarzewicz, T., Kalandyk-Kolodziejczyk, M., Kot, M. and Michalik, A. 2011. Ovary structure and transovarial transmission of endosymbiotic microorganisms in Marchalina hellenica (Insecta, Hemiptera, Coccomorpha: Marchalinidae). —Acta Zoologica (Stockholm) 00:1–9.
The paired ovaries of Marchalina hellenica are composed of about 200 ovarioles of telotrophic type. In each ovariole, a trophic chamber, vitellarium and ovariolar stalk can be distinguished. The tropharia comprise trophocytes and early previtellogenic oocytes (termed arrested oocytes) or trophocytes only. The arrested oocytes are not capable of further development. In the vitellaria, single oocytes develop that are connected to the tropharium by means of broad nutritive cords. The number of germ cells (trophocytes and oocytes) constituting ovarioles is not constant and may range between 25 and 32. Numerous endosymbiotic bacteria occur in the cytoplasm of trophocytes. The endosymbionts are transported via nutritive cords to the developing oocyte. The obtained results are discussed in a phylogenetic context.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00542.x" xmlns="http://purl.org/rss/1.0/"><title>Tentacular apparatus ultrastructure in the larva of Bolinopsis infundibulum (Lobata: Ctenophora)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00542.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Tentacular apparatus ultrastructure in the larva of Bolinopsis infundibulum (Lobata: Ctenophora)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ilya Borisenko, Alexander V. Ereskovsky</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-23T22:06:10.189575-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00542.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00542.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00542.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">193</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">202</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Borisenko, I. and Ereskovsky, A.V. 2011. Tentacular apparatus ultrastructure in the larva of <em>Bolinopsis infundibulum</em> (Lobata: Ctenophora). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–10.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Most ctenophores have a tentacular apparatus, which plays some role in their feeding. Tentacle structure has been described in adults of only three ctenophore species, but the larval tentacles have remained completely unstudied. We made a light and electron microscopic study of the tentacular apparatus in the larvae of <em>Bolinopsis infundibulum</em> from the White Sea. The tentacular apparatus of <em>B. infundibulum</em> larvae consists of the tentacle proper and the tentacle root. The former contains terminally differentiated cells, while the latter contains stem cells and cells undergoing differentiation. The core of the tentacle is formed by myocytes, and its epidermis contains colloblasts (hunting cells), wall cells, degenerating cask cells, refractive vesicles, and ciliated sensory cells. Stem cells, colloblasts, and cask cells at various stages of differentiation and putative myocytes progenitors were revealed in the tentacle root. Two different populations of the stem cells in the tentacle root give rise to epidermal (colloblasts and cask cells) and mesogleal (myocytes) cell lines. Nervous elements, glandular cells, and basal lamina were not found. Step-by-step differentiation of colloblasts and cask cells is described.</p></div>
]]></content:encoded><description>

Borisenko, I. and Ereskovsky, A.V. 2011. Tentacular apparatus ultrastructure in the larva of Bolinopsis infundibulum (Lobata: Ctenophora). —Acta Zoologica (Stockholm) 00: 1–10.
Most ctenophores have a tentacular apparatus, which plays some role in their feeding. Tentacle structure has been described in adults of only three ctenophore species, but the larval tentacles have remained completely unstudied. We made a light and electron microscopic study of the tentacular apparatus in the larvae of Bolinopsis infundibulum from the White Sea. The tentacular apparatus of B. infundibulum larvae consists of the tentacle proper and the tentacle root. The former contains terminally differentiated cells, while the latter contains stem cells and cells undergoing differentiation. The core of the tentacle is formed by myocytes, and its epidermis contains colloblasts (hunting cells), wall cells, degenerating cask cells, refractive vesicles, and ciliated sensory cells. Stem cells, colloblasts, and cask cells at various stages of differentiation and putative myocytes progenitors were revealed in the tentacle root. Two different populations of the stem cells in the tentacle root give rise to epidermal (colloblasts and cask cells) and mesogleal (myocytes) cell lines. Nervous elements, glandular cells, and basal lamina were not found. Step-by-step differentiation of colloblasts and cask cells is described.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00543.x" xmlns="http://purl.org/rss/1.0/"><title>Morphometric differentiation of Pseudocalanus minutus populations in the Barents Sea</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00543.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Morphometric differentiation of Pseudocalanus minutus populations in the Barents Sea</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vladimir G. Dvoretsky, Alexander G. Dvoretsky</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-28T22:54:48.360438-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00543.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00543.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00543.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">203</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">214</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Dvoretsky VG. and Dvoretsky AG. 2011. Morphometric differentiation of <em>Pseudocalanus minutus</em> populations in the Barents Sea. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–12.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We investigated spatial variations in the morphometric characteristics (total length of body, lengths of cephalothorax, abdomen and antennules, and their relative proportions) of <em>Pseudocalanus minutus</em>, an abundant copepod species across the Barents Sea in August–September 2007. Females were found to have higher values for the measured parameters than males. The average absolute morphometric characters of both sexes increased from the south to the north. In most cases, parameters were similar in the southern, central, and eastern regions delineated by cluster analyses of oceanographic variables. The morphometric characteristics were strongly correlated with environmental variables in both males and females. Multiple regression analysis showed that temperature together with salinity explained 72–85% (in females) and 38–91% (in males) of the total variations in the log<sub>10</sub>-transformed morphometric parameters. According to principal component analysis and discriminant function analysis, two distinct groups could be separated in the Barents Sea. The first group included the copepods from the northern region; the other included populations from the southern, central, and eastern regions. The observed morphological variation can be interpreted as geographical variation connected with hydrological variability.</p></div>
]]></content:encoded><description>

Dvoretsky VG. and Dvoretsky AG. 2011. Morphometric differentiation of Pseudocalanus minutus populations in the Barents Sea. —Acta Zoologica (Stockholm) 00: 1–12.
We investigated spatial variations in the morphometric characteristics (total length of body, lengths of cephalothorax, abdomen and antennules, and their relative proportions) of Pseudocalanus minutus, an abundant copepod species across the Barents Sea in August–September 2007. Females were found to have higher values for the measured parameters than males. The average absolute morphometric characters of both sexes increased from the south to the north. In most cases, parameters were similar in the southern, central, and eastern regions delineated by cluster analyses of oceanographic variables. The morphometric characteristics were strongly correlated with environmental variables in both males and females. Multiple regression analysis showed that temperature together with salinity explained 72–85% (in females) and 38–91% (in males) of the total variations in the log10-transformed morphometric parameters. According to principal component analysis and discriminant function analysis, two distinct groups could be separated in the Barents Sea. The first group included the copepods from the northern region; the other included populations from the southern, central, and eastern regions. The observed morphological variation can be interpreted as geographical variation connected with hydrological variability.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00544.x" xmlns="http://purl.org/rss/1.0/"><title>Deconstructing morphology: reply to Scholtz (2010)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00544.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Deconstructing morphology: reply to Scholtz (2010)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nikolaus U. Szucsich, Christian S. Wirkner, Günther Pass</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-21T22:24:36.744693-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00544.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00544.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00544.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">COMMENT</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">215</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">217</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="sec-sum-1" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>Szucsich, N.U., Wirkner C.S. and Pass G. 2011. Deconstructing morphology: reply to Scholtz (2010). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–3</p></div></div>
<div class="section" id="abs1-1" xmlns="http://www.w3.org/1999/xhtml"><h4>Abstract</h4><div class="para"><p>Whenever concepts are taken over into new fields scientists have to take care that these concepts do not become unsubstantial due to ambiguities regarding their applicability. Here we argue why it makes sense to define the homology-concept in a way, so it is applicable for phylogenetic purposes. If used to define the relation among structures of organisms assigned to the same character state of a phylogenetic character, homology has to represent an equivalence relation, with the properties of transitivity and symmetry. This is exactly the reason why correspondence, not similarity should be used to define homology, since the latter is not transitive. Homology then also cannot be used to define the relation among character states of the same phylogenetic character, since this relation necessarily is asymmetric.</p></div></div>
]]></content:encoded><description>

Szucsich, N.U., Wirkner C.S. and Pass G. 2011. Deconstructing morphology: reply to Scholtz (2010). —Acta Zoologica (Stockholm) 00: 1–3


Abstract
Whenever concepts are taken over into new fields scientists have to take care that these concepts do not become unsubstantial due to ambiguities regarding their applicability. Here we argue why it makes sense to define the homology-concept in a way, so it is applicable for phylogenetic purposes. If used to define the relation among structures of organisms assigned to the same character state of a phylogenetic character, homology has to represent an equivalence relation, with the properties of transitivity and symmetry. This is exactly the reason why correspondence, not similarity should be used to define homology, since the latter is not transitive. Homology then also cannot be used to define the relation among character states of the same phylogenetic character, since this relation necessarily is asymmetric.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00545.x" xmlns="http://purl.org/rss/1.0/"><title>A plea for ‘genealogical thinking’ in comparative biology – a rebuttal to the reply of Szucsich, Wirkner, and Pass to my article ‘Deconstructing Morphology’</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00545.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A plea for ‘genealogical thinking’ in comparative biology – a rebuttal to the reply of Szucsich, Wirkner, and Pass to my article ‘Deconstructing Morphology’</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gerhard Scholtz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-23T22:06:13.800047-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00545.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00545.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00545.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">REPLY</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">218</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">221</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Scholtz G. in press. A plea for ‘genealogical thinking’ in comparative biology – a rebuttal to the reply of Szucsich, Wirkner, and Pass to my article ‘Deconstructing Morphology’. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–4.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Szucsich <em>et al.</em> (in press) claim that – in contrast to my statement – morphological thinking has to be ‘cladistic.’ Based on this premise, they stress the difference between the relationships among states of characters versus those among structures assigned to the same character state as implemented in numerical cladistic reasoning. SEA claim that my approach to the homology concept only deals with the problem of the integration of various character states into the same character, whereas the necessary relationships among structures assigned to the same state are not covered. Based on this distinction, SEA also criticise the application of similarity in my definition of homology. Furthermore, they address the issue of evolutionarily independent units.</p></div>
]]></content:encoded><description>

Scholtz G. in press. A plea for ‘genealogical thinking’ in comparative biology – a rebuttal to the reply of Szucsich, Wirkner, and Pass to my article ‘Deconstructing Morphology’. —Acta Zoologica (Stockholm) 00: 1–4.
Szucsich et al. (in press) claim that – in contrast to my statement – morphological thinking has to be ‘cladistic.’ Based on this premise, they stress the difference between the relationships among states of characters versus those among structures assigned to the same character state as implemented in numerical cladistic reasoning. SEA claim that my approach to the homology concept only deals with the problem of the integration of various character states into the same character, whereas the necessary relationships among structures assigned to the same state are not covered. Based on this distinction, SEA also criticise the application of similarity in my definition of homology. Furthermore, they address the issue of evolutionarily independent units.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00546.x" xmlns="http://purl.org/rss/1.0/"><title>Observations on the ultrastructure and distribution of chromatophores in the skin of chelonians</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00546.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Observations on the ultrastructure and distribution of chromatophores in the skin of chelonians</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lorenzo Alibardi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-30T23:04:56.393719-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00546.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00546.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00546.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">222</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">232</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Alibardi, L. 2011. Observations on the ultrastructure and distribution of chromatophores in the skin of chelonians. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>:1–11.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The cytology and distribution of chromatophores responsible for skin pigmentation in chelonians is analyzed. Epidermal melanocytes are involved in the formation of dark spots or stripes in growing shelled and non-shelled skin. Melanocytes rest in the basal layer of the epidermis and transfer melanosomes into keratinocytes during epidermal growth. Dermal melanophores and other chromatophores instead remain in the dermis and form the gray background of the skin. When dermal melanophores condense, they give origin to the dense spots or stripes in areas where no epidermal melanocytes are present. In the latter case, the epidermis and the corneous layer are transparent and reveal the dermal distribution of melanophores and other chromatophores underneath. As a result of this basic process of distribution of pigment cells, the dark areas visible in scales can have a double origin (epidermal and dermal) or a single origin (epidermal or dermal). Xanthophores, lipophores, and a cell containing both pterinosomes and lipid droplets are sparse in the loose dermis while iridophores are rarely seen in the skin of chelonians analyzed in the present study. Xanthophores and lipophores contribute to form the pale, yellow or oranges hues present among the dark areas of the skin in turtles.</p></div>
]]></content:encoded><description>

Alibardi, L. 2011. Observations on the ultrastructure and distribution of chromatophores in the skin of chelonians. —Acta Zoologica (Stockholm) 00:1–11.
The cytology and distribution of chromatophores responsible for skin pigmentation in chelonians is analyzed. Epidermal melanocytes are involved in the formation of dark spots or stripes in growing shelled and non-shelled skin. Melanocytes rest in the basal layer of the epidermis and transfer melanosomes into keratinocytes during epidermal growth. Dermal melanophores and other chromatophores instead remain in the dermis and form the gray background of the skin. When dermal melanophores condense, they give origin to the dense spots or stripes in areas where no epidermal melanocytes are present. In the latter case, the epidermis and the corneous layer are transparent and reveal the dermal distribution of melanophores and other chromatophores underneath. As a result of this basic process of distribution of pigment cells, the dark areas visible in scales can have a double origin (epidermal and dermal) or a single origin (epidermal or dermal). Xanthophores, lipophores, and a cell containing both pterinosomes and lipid droplets are sparse in the loose dermis while iridophores are rarely seen in the skin of chelonians analyzed in the present study. Xanthophores and lipophores contribute to form the pale, yellow or oranges hues present among the dark areas of the skin in turtles.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00548.x" xmlns="http://purl.org/rss/1.0/"><title>The claw closer muscle of two estuarine crab species, Cyrtograpsus angulatus and Neohelice granulata (Grapsoidea, Varunidae): histochemical fibre type composition</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00548.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The claw closer muscle of two estuarine crab species, Cyrtograpsus angulatus and Neohelice granulata (Grapsoidea, Varunidae): histochemical fibre type composition</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">María V. Longo, Alcira O. Díaz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-12T00:26:04.091878-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00548.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00548.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00548.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">233</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">239</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Longo, M.V. and Díaz, A.O. (2011). The claw closer muscle of two estuarine crab species, <em>Cyrtograpsus angulatus</em> and <em>Neohelice granulata</em> (Grapsoidea, Varunidae): histochemical fibre type composition. —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–7.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study permitted the characterization of four types of muscle fibres in the claw closer muscles of <em>Cyrtograpsus angulatus</em> and <em>Neohelice granulata</em>. Succinic dehydrogenase (SDH) for mitochondria, periodic acid Schiff (PAS) for glycogen, Sudan Black B for lipids and myosin-adenosine triphosphatase (m-ATPase) preincubated at alkaline and acid pHs were used for that purpose. The mean fibre diameters, the relative areas and frequencies of each muscle fibre type were calculated. Types I and IV would be considered ‘extreme’ groups with type I fibres large, weak and acid/alkaline-labile m-ATPase, weak SDH, PAS and Sudan, and type IV fibres small, very strong and acid/alkaline-resistant m-ATPase, strong SDH and PAS, and moderate Sudan. Types II and III would belong to a predominant ‘intermediate’ group. Type IV fibres were scarce in <em>C. angulatus</em> but represented 25% of the total fibre population in <em>N. granulata</em>. In <em>C. angulatus</em>, the relative area occupied by type I fibres was bigger than its relative proportion, whereas in <em>N. granulata,</em> types I and II had similar patterns. Concluding, variations in fibre type composition in the claw closer muscles of <em>C. angulatus</em> and <em>N. granulata</em> would be linked to different habitats and feeding behaviours.</p></div>
]]></content:encoded><description>

Longo, M.V. and Díaz, A.O. (2011). The claw closer muscle of two estuarine crab species, Cyrtograpsus angulatus and Neohelice granulata (Grapsoidea, Varunidae): histochemical fibre type composition. —Acta Zoologica (Stockholm) 00: 1–7.
This study permitted the characterization of four types of muscle fibres in the claw closer muscles of Cyrtograpsus angulatus and Neohelice granulata. Succinic dehydrogenase (SDH) for mitochondria, periodic acid Schiff (PAS) for glycogen, Sudan Black B for lipids and myosin-adenosine triphosphatase (m-ATPase) preincubated at alkaline and acid pHs were used for that purpose. The mean fibre diameters, the relative areas and frequencies of each muscle fibre type were calculated. Types I and IV would be considered ‘extreme’ groups with type I fibres large, weak and acid/alkaline-labile m-ATPase, weak SDH, PAS and Sudan, and type IV fibres small, very strong and acid/alkaline-resistant m-ATPase, strong SDH and PAS, and moderate Sudan. Types II and III would belong to a predominant ‘intermediate’ group. Type IV fibres were scarce in C. angulatus but represented 25% of the total fibre population in N. granulata. In C. angulatus, the relative area occupied by type I fibres was bigger than its relative proportion, whereas in N. granulata, types I and II had similar patterns. Concluding, variations in fibre type composition in the claw closer muscles of C. angulatus and N. granulata would be linked to different habitats and feeding behaviours.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00549.x" xmlns="http://purl.org/rss/1.0/"><title>Spermatological characters in the diphyllobothriidean Schistocephalus solidus (Cestoda)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00549.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Spermatological characters in the diphyllobothriidean Schistocephalus solidus (Cestoda)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Céline Levron, Aneta Yoneva, Martin Kalbe</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-12T00:27:11.882046-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1463-6395.2011.00549.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1463-6395.2011.00549.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1463-6395.2011.00549.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">240</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">247</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Levron, C., Yoneva, A. and Kalbe, M. 2011. Spermatological characters in the diphyllobothriidean <em>Schistocephalus solidus</em> (Cestoda). —<em>Acta Zoologica</em> (Stockholm) <b>00</b>: 1–8.</p></div>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The spermiogenesis and the mature spermatozoon of <em>Schistocephalus solidus</em> (Cestoda: Diphyllobothriidea) are described using transmission electron microscopy. Spermiogenesis in <em>S. solidus</em> begins with the formation in the spermatid of a differentiation zone surrounded by cortical microtubules and delimited by arching membranes. This conical area presents two centrioles associated with striated rootlets and a median cytoplasmic extension between them. The centrioles are separated by an intercentriolar body composed of three electron-dense plates dividing four electron-lucent plates. The centrioles give rise to two flagella that undergo a rotation and later fuse proximodistally with the median cytoplasmic expansion. The presence of an electron-dense material in the distal part of the differentiation zone is observed in the early stage of spermiogenesis. This pattern corresponds to Type I spermiogenesis according to the classification proposed by Bâ and Marchand (<em>Mémoires du Muséum National d’Histoire Naturelle</em> 1995; <b>166</b>: 87). The mature spermatozoon of <em>S. solidus</em> presents the Type I pattern defined by Levron <em>et al.</em> (<em>Biological Reviews</em> 2010; <b>85</b>: 523). It consists of five regions that exhibit two axonemes, parallel cortical microtubules, nucleus and electron-dense zones. The anterior tip of the spermatozoon possesses only a few singlets. The axonemes are of a 9 + ’1’ trepaxonematan pattern and do not reach the posterior extremity of the mature spermatozoon.</p></div>
]]></content:encoded><description>

Levron, C., Yoneva, A. and Kalbe, M. 2011. Spermatological characters in the diphyllobothriidean Schistocephalus solidus (Cestoda). —Acta Zoologica (Stockholm) 00: 1–8.
The spermiogenesis and the mature spermatozoon of Schistocephalus solidus (Cestoda: Diphyllobothriidea) are described using transmission electron microscopy. Spermiogenesis in S. solidus begins with the formation in the spermatid of a differentiation zone surrounded by cortical microtubules and delimited by arching membranes. This conical area presents two centrioles associated with striated rootlets and a median cytoplasmic extension between them. The centrioles are separated by an intercentriolar body composed of three electron-dense plates dividing four electron-lucent plates. The centrioles give rise to two flagella that undergo a rotation and later fuse proximodistally with the median cytoplasmic expansion. The presence of an electron-dense material in the distal part of the differentiation zone is observed in the early stage of spermiogenesis. This pattern corresponds to Type I spermiogenesis according to the classification proposed by Bâ and Marchand (Mémoires du Muséum National d’Histoire Naturelle 1995; 166: 87). The mature spermatozoon of S. solidus presents the Type I pattern defined by Levron et al. (Biological Reviews 2010; 85: 523). It consists of five regions that exhibit two axonemes, parallel cortical microtubules, nucleus and electron-dense zones. The anterior tip of the spermatozoon possesses only a few singlets. The axonemes are of a 9 + ’1’ trepaxonematan pattern and do not reach the posterior extremity of the mature spermatozoon.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12026" xmlns="http://purl.org/rss/1.0/"><title>Lumbar glands in the frog genera Pleurodema and Somuncuria (Anura: Leiuperidae): histological and histochemical perspectives</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12026</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Lumbar glands in the frog genera Pleurodema and Somuncuria (Anura: Leiuperidae): histological and histochemical perspectives</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-06T22:27:33.772413-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/azo.12026</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/azo.12026</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fazo.12026</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Corrigendum</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">248</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">248</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item></rdf:RDF>