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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"><channel rdf:about="http://onlinelibrary.wiley.com/rss/journal/10.1111/(ISSN)1744-7410" xmlns="http://purl.org/rss/1.0/"><title>Invertebrate Biology</title><description> Wiley Online Library : Invertebrate Biology</description><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2F%28ISSN%291744-7410</link><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc</dc:publisher><dc:language xmlns:dc="http://purl.org/dc/elements/1.1/">en</dc:language><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/">© American Microscopical Society</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1077-8306</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1744-7410</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">March 2013</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">132</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">80</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/ivb.2013.132.issue-1/asset/cover.gif?v=1&amp;s=63b05cbeeb55fb6f5e6fa6b4a27ec6506ed473c0"/><items><rdf:Seq><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12019"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12018"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12020"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12017"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12016"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12010"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12014"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12012"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12004"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12008"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12011"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12009"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12013"/></rdf:Seq></items></channel><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12019" xmlns="http://purl.org/rss/1.0/"><title>Relationship between environmental variables and surface activity of scorpions in the Arid Chaco ecoregion of Argentina</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12019</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Relationship between environmental variables and surface activity of scorpions in the Arid Chaco ecoregion of Argentina</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mónica F. Nime, Fernando Casanoves, David E. Vrech, Camilo I. Mattoni</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T10:41:26.313425-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12019</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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>Many environmental factors may influence the activity of scorpions in arid ecosystems. In this study, we examined the effects of such factors on scorpion activity at a mature and a secondary forest site in the Chancaní Reserve (Arid Chaco ecoregion in Córdoba, Argentina). Scorpions were collected using pitfall traps, and their nocturnal activity was observed by means of UV light during 14 nights. Temperature, air humidity, atmospheric pressure, and wind velocity were measured, and the percentage of visible moon was estimated. A total of 440 scorpions, representing seven species belonging to two families (Bothriuridae and Buthidae), were observed in the study area. <em>Brachistosternus ferrugineus</em> was the species most commonly observed using both methods. Mature and secondary forest shared slightly more than 50% of species. Surface activity of scorpions observed with the two methods differed significantly between the two areas. Surface activity of all scorpions and of <em>B. ferrugineus</em> were negatively related to the phase of the moon and positively related to air temperature. Physical factors thus have important effects on scorpion activity.</p></div>
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Many environmental factors may influence the activity of scorpions in arid ecosystems. In this study, we examined the effects of such factors on scorpion activity at a mature and a secondary forest site in the Chancaní Reserve (Arid Chaco ecoregion in Córdoba, Argentina). Scorpions were collected using pitfall traps, and their nocturnal activity was observed by means of UV light during 14 nights. Temperature, air humidity, atmospheric pressure, and wind velocity were measured, and the percentage of visible moon was estimated. A total of 440 scorpions, representing seven species belonging to two families (Bothriuridae and Buthidae), were observed in the study area. Brachistosternus ferrugineus was the species most commonly observed using both methods. Mature and secondary forest shared slightly more than 50% of species. Surface activity of scorpions observed with the two methods differed significantly between the two areas. Surface activity of all scorpions and of B. ferrugineus were negatively related to the phase of the moon and positively related to air temperature. Physical factors thus have important effects on scorpion activity.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12018" xmlns="http://purl.org/rss/1.0/"><title>Host autophagic degradation and associated symbiont loss in response to heat stress in the symbiotic anemone, Aiptasia pallida</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12018</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Host autophagic degradation and associated symbiont loss in response to heat stress in the symbiotic anemone, Aiptasia pallida</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shanna D. Hanes, Stephen C. Kempf</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T10:41:09.961167-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12018</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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>Coral bleaching involves the loss of essential photosynthetic dinoflagellates (<em>Symbiodinium</em> sp.) from host gastrodermal cells in response to temperature or light stress. Although numerous potential cellular bleaching mechanisms have been proposed, there remains much uncertainty regarding which cellular events occur during early breakdown of the host–dinoflagellate symbiosis. In this study, transmission electron microscopy was used to conduct a detailed examination of symbiotic tissues of the tropical anemone <em>Aiptasia pallida</em> during early stages of host stress. Bleaching was induced by exposing specimens to a stress treatment of 32.5±0.5°C at 140±7<sup> </sup>μ mol photons m<sup>−2</sup> s<sup>−1</sup> light intensity for 12 h, followed by 12 h at 24±1°C in darkness, repeated over a 48 h period. Ultrastructural examinations revealed numerous dense autophagic structures and associated cellular degradation in tentacle tissues after ~12 h of the stress treatment. Anemones treated with rapamycin, a known autophagy inducer, exhibited the same ultrastructural characteristics as heat-stressed tissues, confirming that the structures observed during heat stress treatment were autophagic. In addition, symbionts appeared to be expelled from host cells via an apocrine-like detachment mechanism from the apical ends of autophagic gastrodermal cells. This study provides the first ultrastructural evidence of host autophagic degradation during thermal stress in a cnidarian system and also supports earlier suggestions that autophagy is an active cellular mechanism during early stages of bleaching.</p></div>
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Coral bleaching involves the loss of essential photosynthetic dinoflagellates (Symbiodinium sp.) from host gastrodermal cells in response to temperature or light stress. Although numerous potential cellular bleaching mechanisms have been proposed, there remains much uncertainty regarding which cellular events occur during early breakdown of the host–dinoflagellate symbiosis. In this study, transmission electron microscopy was used to conduct a detailed examination of symbiotic tissues of the tropical anemone Aiptasia pallida during early stages of host stress. Bleaching was induced by exposing specimens to a stress treatment of 32.5±0.5°C at 140±7 μ mol photons m−2 s−1 light intensity for 12 h, followed by 12 h at 24±1°C in darkness, repeated over a 48 h period. Ultrastructural examinations revealed numerous dense autophagic structures and associated cellular degradation in tentacle tissues after ~12 h of the stress treatment. Anemones treated with rapamycin, a known autophagy inducer, exhibited the same ultrastructural characteristics as heat-stressed tissues, confirming that the structures observed during heat stress treatment were autophagic. In addition, symbionts appeared to be expelled from host cells via an apocrine-like detachment mechanism from the apical ends of autophagic gastrodermal cells. This study provides the first ultrastructural evidence of host autophagic degradation during thermal stress in a cnidarian system and also supports earlier suggestions that autophagy is an active cellular mechanism during early stages of bleaching.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12020" xmlns="http://purl.org/rss/1.0/"><title>Survival and colonization of nematodes in a composting process</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12020</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Survival and colonization of nematodes in a composting process</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hanne Steel, Freija Verdoodt, Andrea Čerevková, Marjolein Couvreur, Pamela Fonderie, Tom Moens, Wim Bert</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T10:41:03.064519-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12020</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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>Nematodes are omnipresent in composts and are active in virtually all stages of the composting process. Major shifts in species composition, life strategies, and feeding behavior occur during the composting process. Due to the heat peak, nematodes can be virtually absent, but several taxa appear immediately when the temperatures drop. These comprise both taxa present before the heat peak and new taxa. However, it is not known how nematodes populate the compost. In this study, we aimed to assess the survival and colonization capacity of nematodes in compost. Our results showed that composting processes inaccessible to insects or not in contact with soil did not significantly influence nematode succession during composting. However, differences between treatments were found for some specific taxa (i.e., for <em>Acrostichus</em> sp., Neodiplogasteridae sp., <em>Nygolaimoides</em> sp., and Rhabditidae sp. 1), illustrating the importance of insects for the dispersal of nematodes to compost. Experiments in the lab with the blue bottle fly as a possible carrier demonstrated actual transport of nematodes isolated from compost by the fly (i.e., <em>Halicephalobus</em> cfr. <em>gingivalis</em>,<em> Diploscapter coronatus</em>,<em> Diplogasteritus</em> sp., <em>Acrostichus</em> sp., and <em>Mesorhabditis</em> sp.). Juveniles and dauer stages of <em>Aphelenchoides</em> sp., <em>Panagrolaimus</em> sp., and rhabditids survived an experimentally induced temperature peak, while members of Tylenchidae did not. In conclusion, our results indicate that the rapidly changing nematode community in compost is the result of both differential survival and colonization capacities.</p></div>
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Nematodes are omnipresent in composts and are active in virtually all stages of the composting process. Major shifts in species composition, life strategies, and feeding behavior occur during the composting process. Due to the heat peak, nematodes can be virtually absent, but several taxa appear immediately when the temperatures drop. These comprise both taxa present before the heat peak and new taxa. However, it is not known how nematodes populate the compost. In this study, we aimed to assess the survival and colonization capacity of nematodes in compost. Our results showed that composting processes inaccessible to insects or not in contact with soil did not significantly influence nematode succession during composting. However, differences between treatments were found for some specific taxa (i.e., for Acrostichus sp., Neodiplogasteridae sp., Nygolaimoides sp., and Rhabditidae sp. 1), illustrating the importance of insects for the dispersal of nematodes to compost. Experiments in the lab with the blue bottle fly as a possible carrier demonstrated actual transport of nematodes isolated from compost by the fly (i.e., Halicephalobus cfr. gingivalis, Diploscapter coronatus, Diplogasteritus sp., Acrostichus sp., and Mesorhabditis sp.). Juveniles and dauer stages of Aphelenchoides sp., Panagrolaimus sp., and rhabditids survived an experimentally induced temperature peak, while members of Tylenchidae did not. In conclusion, our results indicate that the rapidly changing nematode community in compost is the result of both differential survival and colonization capacities.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12017" xmlns="http://purl.org/rss/1.0/"><title>Longevity costs of same-sex interactions: first evidence from a parasitic wasp</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12017</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Longevity costs of same-sex interactions: first evidence from a parasitic wasp</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Giovanni Benelli, Gabriele Gennari, Alessandra Francini, Angelo Canale</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T10:40:57.706515-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12017</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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>Costs of sexual interactions play a key role in life-history evolution. Although the costs of reproduction have been investigated in both sexes of many insects, the costs of same-sex interactions have been examined in few species. In parasitic wasps, very little has been reported about the longevity costs of heterosexual interactions, and nothing is known about longevity costs of same-sex interactions. In this study, the effects of heterosexual and homosexual activities on longevity were evaluated in <em>Psyttalia concolor</em> (Hymenoptera: Braconidae), a synovigenic koinobiont larval-pupal endoparasitoid of tephritid flies. When compared with individually housed virgin wasps, male longevity was strongly reduced both in males kept with females, and in males kept with other males. When females were kept with males, their longevity was reduced compared with the virgin females and females kept with other females. Overall, the costs of male–female interactions were considerable in both sexes of <em>P. concolor</em>, while same-sex activities were found to be costly only among males, suggesting that they may have implications for the evolution of the <em>P. concolor</em> mating system.</p></div>
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Costs of sexual interactions play a key role in life-history evolution. Although the costs of reproduction have been investigated in both sexes of many insects, the costs of same-sex interactions have been examined in few species. In parasitic wasps, very little has been reported about the longevity costs of heterosexual interactions, and nothing is known about longevity costs of same-sex interactions. In this study, the effects of heterosexual and homosexual activities on longevity were evaluated in Psyttalia concolor (Hymenoptera: Braconidae), a synovigenic koinobiont larval-pupal endoparasitoid of tephritid flies. When compared with individually housed virgin wasps, male longevity was strongly reduced both in males kept with females, and in males kept with other males. When females were kept with males, their longevity was reduced compared with the virgin females and females kept with other females. Overall, the costs of male–female interactions were considerable in both sexes of P. concolor, while same-sex activities were found to be costly only among males, suggesting that they may have implications for the evolution of the P. concolor mating system.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12016" xmlns="http://purl.org/rss/1.0/"><title>Chromatophore radial muscle fibers anchor in flexible squid skin</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12016</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Chromatophore radial muscle fibers anchor in flexible squid skin</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">George R.R. Bell, Alan M. Kuzirian, Stephen L. Senft, Lydia M. Mäthger, Trevor J. Wardill, Roger T. Hanlon</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T10:40:52.319349-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12016</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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>Cephalopod skin is soft, flexible, and produces rapid color changes for camouflage and signaling primarily by regulating the shapes of its numerous chromatophore organs. Each chromatophore has 10–30 radial muscle cells, termed fibers, under central nervous system control. Each fiber contains myofilaments that contract in concert to stretch the pigment-containing cell from its punctate, spherical state to a fully expanded thin disk of color. Expansion occurs in less than one second and can result in a 14-fold expansion in pigment cell diameter. We investigated the anchoring mechanism of radial muscle fibers that expand pigment cells in the longfin squid, <em>Doryteuthis (Loligo) pealeii</em>. The proximal Active Zone of a radial muscle fiber adheres to the pigment cell within an ensheathing sinus. The distal portion forms terminal arbors, thereby increasing the surface area, to adhere it to the dermal extracellular matrix (ECM). While the muscle fiber is attached to the pigment cell with haptosomes, the remainder of the fiber is adhered to the surrounding basal lamina (part of the ECM) by numerous, closely spaced, small costamere-like projections. Branching of the radial muscle fiber termini and the costamere-like attachments are key anatomical specializations that anchor the radial muscle fibers in the pliable skin while allowing the freedom of movement required for large changes in pigment cell diameter. We postulate that these features may be relevant for the development of soft actuation models in materials science.</p></div>
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Cephalopod skin is soft, flexible, and produces rapid color changes for camouflage and signaling primarily by regulating the shapes of its numerous chromatophore organs. Each chromatophore has 10–30 radial muscle cells, termed fibers, under central nervous system control. Each fiber contains myofilaments that contract in concert to stretch the pigment-containing cell from its punctate, spherical state to a fully expanded thin disk of color. Expansion occurs in less than one second and can result in a 14-fold expansion in pigment cell diameter. We investigated the anchoring mechanism of radial muscle fibers that expand pigment cells in the longfin squid, Doryteuthis (Loligo) pealeii. The proximal Active Zone of a radial muscle fiber adheres to the pigment cell within an ensheathing sinus. The distal portion forms terminal arbors, thereby increasing the surface area, to adhere it to the dermal extracellular matrix (ECM). While the muscle fiber is attached to the pigment cell with haptosomes, the remainder of the fiber is adhered to the surrounding basal lamina (part of the ECM) by numerous, closely spaced, small costamere-like projections. Branching of the radial muscle fiber termini and the costamere-like attachments are key anatomical specializations that anchor the radial muscle fibers in the pliable skin while allowing the freedom of movement required for large changes in pigment cell diameter. We postulate that these features may be relevant for the development of soft actuation models in materials science.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12010" xmlns="http://purl.org/rss/1.0/"><title>The triradiate sucking pharynx in animal phylogeny</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12010</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The triradiate sucking pharynx in animal phylogeny</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Claus Nielsen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-21T12:47:18.411526-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12010</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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/">1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">13</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>Independent sucking/swallowing pharynges, as found in members of at least ten animal phyla, are pharynges that are opened by muscles that are not attached to the outer body wall. Their musculature is derived from either mesoderm or ectoderm, the latter taking the form of a myoepithelium. I review results of previous work on the morphology of independent sucking/swallowing pharynges among invertebrates and provide new information on the ultrastructure of the pharynx of the cyclostome bryozoan <em>Crisia eburnea</em>. The various morphologies of this type of pharynx have been used in some phylogenetic considerations, but only the myoepithelial sucking pharynx with a triradiate lumen was considered significant in analyses of relationships between phyla. However, I argue that this shape is the only one that makes an efficient suction pump, and this, together with different orientations of the myoepithelial pharyngeal pump and its phylogenetic distribution, indicates that the triradiate myoepithelial pharynx has evolved convergently in a number of lineages.</p></div>
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Independent sucking/swallowing pharynges, as found in members of at least ten animal phyla, are pharynges that are opened by muscles that are not attached to the outer body wall. Their musculature is derived from either mesoderm or ectoderm, the latter taking the form of a myoepithelium. I review results of previous work on the morphology of independent sucking/swallowing pharynges among invertebrates and provide new information on the ultrastructure of the pharynx of the cyclostome bryozoan Crisia eburnea. The various morphologies of this type of pharynx have been used in some phylogenetic considerations, but only the myoepithelial sucking pharynx with a triradiate lumen was considered significant in analyses of relationships between phyla. However, I argue that this shape is the only one that makes an efficient suction pump, and this, together with different orientations of the myoepithelial pharyngeal pump and its phylogenetic distribution, indicates that the triradiate myoepithelial pharynx has evolved convergently in a number of lineages.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12014" xmlns="http://purl.org/rss/1.0/"><title>Neural correlates of settlement in veliger larvae of the gastropod, Crepidula fornicata</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12014</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Neural correlates of settlement in veliger larvae of the gastropod, Crepidula fornicata</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jacob R. Penniman, Margaret K. Doll, Anthony Pires</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-05T14:35:32.324946-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12014</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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/">14</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">26</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>Settlement behavior of molluscan veliger larvae prior to metamorphosis requires cessation of swimming, accomplished by arrest of prototrochal cilia on the margin of the velum (the larval swimming organ). Ciliary arrest in larvae of gastropods is mediated by an action potential that occurs synchronously across the velum as a consequence of electrical coupling between the prototrochal ciliated cells. We developed a preparation for extracellular recording of such ciliary arrest spikes from intact swimming and crawling veliger larvae of the caenogastropod <em>Crepidula fornicata</em>, using a fine wire electrode. Ciliary arrest spike rates during bouts of substrate crawling were significantly higher than those recorded during preceding swimming periods in larvae that were competent for metamorphosis, but not in precompetent larvae. Spike rates were similar on clean polystyrene substrates, and on substrates that had been coated with a natural cue for metamorphosis (mucus from conspecific adults). We used immunohistochemical methods to localize neuromodulators that might regulate the function of velar cilia. Labeled terminals for serotonin, FMRFamide, and tyrosine hydroxylase (an enzyme for catecholamine synthesis) were located in positions consistent with modulatory effects on the prototrochal ciliated cells. Prototrochal ciliary arrest spike rates and beat frequencies were measured in isolated velar lobes from competent larvae, which were exposed to serotonin, FMRFamide, and dopamine (10<sup>−5</sup> mol L<sup>−1</sup>). Serotonin abolished arrest spiking and increased beat frequency; dopamine also increased beat frequency, and FMRFamide depressed it. Competent larvae tested in a small static water column swam to the top of the column when exposed to serotonin, but occupied lower positions than controls when in the presence of dopamine and FMRFamide. The larval nervous system appears to regulate velar functions that are critical for settlement behavior, and is likely to do so by integrating different sensory modalities in an age-dependent manner.</p></div>
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Settlement behavior of molluscan veliger larvae prior to metamorphosis requires cessation of swimming, accomplished by arrest of prototrochal cilia on the margin of the velum (the larval swimming organ). Ciliary arrest in larvae of gastropods is mediated by an action potential that occurs synchronously across the velum as a consequence of electrical coupling between the prototrochal ciliated cells. We developed a preparation for extracellular recording of such ciliary arrest spikes from intact swimming and crawling veliger larvae of the caenogastropod Crepidula fornicata, using a fine wire electrode. Ciliary arrest spike rates during bouts of substrate crawling were significantly higher than those recorded during preceding swimming periods in larvae that were competent for metamorphosis, but not in precompetent larvae. Spike rates were similar on clean polystyrene substrates, and on substrates that had been coated with a natural cue for metamorphosis (mucus from conspecific adults). We used immunohistochemical methods to localize neuromodulators that might regulate the function of velar cilia. Labeled terminals for serotonin, FMRFamide, and tyrosine hydroxylase (an enzyme for catecholamine synthesis) were located in positions consistent with modulatory effects on the prototrochal ciliated cells. Prototrochal ciliary arrest spike rates and beat frequencies were measured in isolated velar lobes from competent larvae, which were exposed to serotonin, FMRFamide, and dopamine (10−5 mol L−1). Serotonin abolished arrest spiking and increased beat frequency; dopamine also increased beat frequency, and FMRFamide depressed it. Competent larvae tested in a small static water column swam to the top of the column when exposed to serotonin, but occupied lower positions than controls when in the presence of dopamine and FMRFamide. The larval nervous system appears to regulate velar functions that are critical for settlement behavior, and is likely to do so by integrating different sensory modalities in an age-dependent manner.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12012" xmlns="http://purl.org/rss/1.0/"><title>Androdioecy and hermaphroditism in five species of clam shrimps (Crustacea: Branchiopoda: Spinicaudata) from India and Thailand</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12012</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Androdioecy and hermaphroditism in five species of clam shrimps (Crustacea: Branchiopoda: Spinicaudata) from India and Thailand</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Justin S. Brantner, Donald W. Ott, R. Joel Duff, La-orsri Sanoamuang, Gulli Palli Simhachalam, K. K. Subhash Babu, Stephen C. Weeks</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-19T13:27:40.313191-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12012</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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/">27</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">37</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>Crustaceans in the order Spinicaudata display a broad range of reproductive strategies, ranging from pure hermaphroditism to pure dioecy (separate males and females), and intermediate combinations. One particularly interesting genus of these “clam shrimps” is <em>Eulimnadia</em>. Based on offspring sex ratios, it has been suggested that all members of the genus are androdioecious: populations consist of mixtures of males and hermaphrodites. However, only two of the ~40 species in this genus have been examined histologically to confirm the presence of ovotestes in the purported hermaphrodites of this group. Here, we report both sex ratio and histological evidence showing that populations of five additional <em>Eulimnadia</em> species from India and Thailand are indeed mixes of males and hermaphrodites (four species) or hermaphrodite only (one species). Sex ratios of adults and offspring from isolated hermaphrodites are in accordance with those previously reported for 15 <em>Eulimnadia</em> species, and histological assays of four of the five species show the presence of both testicular and ovarian tissue in these hermaphrodites. As has been previously reported, the testicular tissue in members of these <em>Eulimnadia</em> spp. is located in a small section at the distal end of the gonad. In addition, the sperm produced in these hermaphrodites forms distinct plaques of compacted chromatin. Overall, these data are consistent with a single origin of hermaphroditism in <em>Eulimnadia</em>, and support the notion that all members of the genus are either androdioecious or all-hermaphroditic.</p></div>
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Crustaceans in the order Spinicaudata display a broad range of reproductive strategies, ranging from pure hermaphroditism to pure dioecy (separate males and females), and intermediate combinations. One particularly interesting genus of these “clam shrimps” is Eulimnadia. Based on offspring sex ratios, it has been suggested that all members of the genus are androdioecious: populations consist of mixtures of males and hermaphrodites. However, only two of the ~40 species in this genus have been examined histologically to confirm the presence of ovotestes in the purported hermaphrodites of this group. Here, we report both sex ratio and histological evidence showing that populations of five additional Eulimnadia species from India and Thailand are indeed mixes of males and hermaphrodites (four species) or hermaphrodite only (one species). Sex ratios of adults and offspring from isolated hermaphrodites are in accordance with those previously reported for 15 Eulimnadia species, and histological assays of four of the five species show the presence of both testicular and ovarian tissue in these hermaphrodites. As has been previously reported, the testicular tissue in members of these Eulimnadia spp. is located in a small section at the distal end of the gonad. In addition, the sperm produced in these hermaphrodites forms distinct plaques of compacted chromatin. Overall, these data are consistent with a single origin of hermaphroditism in Eulimnadia, and support the notion that all members of the genus are either androdioecious or all-hermaphroditic.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12004" xmlns="http://purl.org/rss/1.0/"><title>Morphological diversity of setae on the second maxilliped of fiddler crabs (Decapoda: Ocypodidae) from the southwestern Atlantic coast</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12004</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Morphological diversity of setae on the second maxilliped of fiddler crabs (Decapoda: Ocypodidae) from the southwestern Atlantic coast</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Karine Delevati Colpo, Maria Lucia Negreiros-Fransozo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-19T13:22:27.162288-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12004</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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/">38</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">45</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>Fiddler crabs are deposit feeders, and use the setae on their mouth appendages to manipulate sediment particles to extract food. The number of spoon-tipped setae on the second maxilliped is frequently related to the distribution of fiddler crabs on estuarine sediments, but no study has compared the morphological diversity of these setae among multiple fiddler crab species. Here, we describe and classify the setae of the second maxillipeds of the nine <em>Uca</em> spp. known from the Brazilian coast. The second maxilliped of each species was examined by scanning electron microscopy. Six types of setae (five papposerrate, and one pappose) were described on the meropodite of the second maxilliped. Among the papposerrate setae, one type had a spoon-like tip, and the morphology of this type, especially the degree of curvature, differed between species. Members of <em>Uca leptodactylus</em>,<em> U. uruguayensis,</em> and <em>U. maracoani</em> had highly concave spoon-tipped setae. In <em>U. rapax</em> and <em>U. cumulanta</em>, the setal tip was moderately curved, while in <em>U. thayeri</em>,<em> U. burgersi,</em> and <em>U. mordax,</em> this curvature was slight. At the other extreme, the meropodite of the second maxilliped of <em>U. vocator</em> lacked setae altogether. This is the first study that describes differences in the degree of curvature of spoon-tipped setae in fiddler crabs. This trait may be strongly related to the distribution of these fiddler crabs on different estuarine substrates.</p></div>
]]></content:encoded><description>

Fiddler crabs are deposit feeders, and use the setae on their mouth appendages to manipulate sediment particles to extract food. The number of spoon-tipped setae on the second maxilliped is frequently related to the distribution of fiddler crabs on estuarine sediments, but no study has compared the morphological diversity of these setae among multiple fiddler crab species. Here, we describe and classify the setae of the second maxillipeds of the nine Uca spp. known from the Brazilian coast. The second maxilliped of each species was examined by scanning electron microscopy. Six types of setae (five papposerrate, and one pappose) were described on the meropodite of the second maxilliped. Among the papposerrate setae, one type had a spoon-like tip, and the morphology of this type, especially the degree of curvature, differed between species. Members of Uca leptodactylus, U. uruguayensis, and U. maracoani had highly concave spoon-tipped setae. In U. rapax and U. cumulanta, the setal tip was moderately curved, while in U. thayeri, U. burgersi, and U. mordax, this curvature was slight. At the other extreme, the meropodite of the second maxilliped of U. vocator lacked setae altogether. This is the first study that describes differences in the degree of curvature of spoon-tipped setae in fiddler crabs. This trait may be strongly related to the distribution of these fiddler crabs on different estuarine substrates.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12008" xmlns="http://purl.org/rss/1.0/"><title>Population dynamics of a threatened giant millipede: implications for restoration</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12008</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Population dynamics of a threatened giant millipede: implications for restoration</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">James M. Lawrence, Michael J. Samways, Janine A. Kelly, Jock Henwood</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-15T12:40:37.819338-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12008</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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/">46</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">51</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 population dynamics of threatened invertebrates have important implications for their conservation and restoration. The Seychelles giant millipede (SGM), <em>Sechelleptus seychellarum</em>, is a threatened and functionally important macro-detritivore endemic to the Seychelles granitic islands. Here, we studied the population dynamics of the SGM from 1998 to 2009 on Cousine Island, Seychelles, to make practical restoration recommendations. Large fluctuations in millipede densities were found between 1998 and 2009. In 2002, 2003, 2005, and 2007 millipede densities were low, while densities were high in 1998 and 2009. Although the SGM is active all year round, millipede surface activity was positively correlated with rainfall, with millipede density high during the wet NW monsoon period (i.e., October to April) and low during the SE trade wind period (i.e., May to September). Female:male:juvenile ratios were ∼3:1:1. The implications of these results for restoration are that translocations should preferably be done in years of high millipede densities and during the wet season. Furthermore, chemical control of the invasive ant <em>Pheidole megacephala</em>, which is currently being carried out on Cousine Island and in future could be conducted on other Seychelles islands, should preferably be done during the low rainfall months, as the SGM readily consumes the hydramethylnon-based bait.</p></div>
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The population dynamics of threatened invertebrates have important implications for their conservation and restoration. The Seychelles giant millipede (SGM), Sechelleptus seychellarum, is a threatened and functionally important macro-detritivore endemic to the Seychelles granitic islands. Here, we studied the population dynamics of the SGM from 1998 to 2009 on Cousine Island, Seychelles, to make practical restoration recommendations. Large fluctuations in millipede densities were found between 1998 and 2009. In 2002, 2003, 2005, and 2007 millipede densities were low, while densities were high in 1998 and 2009. Although the SGM is active all year round, millipede surface activity was positively correlated with rainfall, with millipede density high during the wet NW monsoon period (i.e., October to April) and low during the SE trade wind period (i.e., May to September). Female:male:juvenile ratios were ∼3:1:1. The implications of these results for restoration are that translocations should preferably be done in years of high millipede densities and during the wet season. Furthermore, chemical control of the invasive ant Pheidole megacephala, which is currently being carried out on Cousine Island and in future could be conducted on other Seychelles islands, should preferably be done during the low rainfall months, as the SGM readily consumes the hydramethylnon-based bait.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12011" xmlns="http://purl.org/rss/1.0/"><title>Inverted sand dollars actively orient themselves in flow to increase likelihood of righting</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12011</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Inverted sand dollars actively orient themselves in flow to increase likelihood of righting</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adam R. Hardy, Rachel A. Merz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-07T14:23:08.597512-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12011</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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/">52</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">61</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 fact that sand dollars are often dislodged and inverted is an inescapable consequence of living at or slightly below the sediment–water interface. Once inverted, however, how do sand dollars effectively right themselves, given their small spines and stiff internal skeletons? Here, we examined the possibility that individuals of <em>Mellita quinquiesperforata</em> and <em>Dendraster excentricus</em> may take advantage of the interaction of their morphology and flow to increase the likelihood of righting. Based on flow tank observations, the critical velocity required to flip an inverted sand dollar varies with orientation and increases with test size. For both species, the critical velocity was lower when inverted sand dollars were oriented with the posterior margin facing directly downstream, compared with when the posterior margin was positioned in an upstream orientation. To test whether inverted sand dollars would actively rotate into a more advantageous position for flipping, we exposed inverted animals in three starting orientations – with their posterior edge directed upstream (the least favored position for flipping), perpendicular, and downstream to flow – to the minimum flow expected to induce flipping and compared their responses. Time-lapse photography showed that regardless of initial orientation, within one hour, a majority of individuals of both species rotated into positions that were not statistically different from the downstream orientation (the most favored position for flipping). These results for <em>D. excentricus</em> were further confirmed in a field experiment. Taken together, these data suggest that inverted sand dollars are able to recognize flow direction and respond by modifying their orientation to maximize lift and drag for righting.</p></div>
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The fact that sand dollars are often dislodged and inverted is an inescapable consequence of living at or slightly below the sediment–water interface. Once inverted, however, how do sand dollars effectively right themselves, given their small spines and stiff internal skeletons? Here, we examined the possibility that individuals of Mellita quinquiesperforata and Dendraster excentricus may take advantage of the interaction of their morphology and flow to increase the likelihood of righting. Based on flow tank observations, the critical velocity required to flip an inverted sand dollar varies with orientation and increases with test size. For both species, the critical velocity was lower when inverted sand dollars were oriented with the posterior margin facing directly downstream, compared with when the posterior margin was positioned in an upstream orientation. To test whether inverted sand dollars would actively rotate into a more advantageous position for flipping, we exposed inverted animals in three starting orientations – with their posterior edge directed upstream (the least favored position for flipping), perpendicular, and downstream to flow – to the minimum flow expected to induce flipping and compared their responses. Time-lapse photography showed that regardless of initial orientation, within one hour, a majority of individuals of both species rotated into positions that were not statistically different from the downstream orientation (the most favored position for flipping). These results for D. excentricus were further confirmed in a field experiment. Taken together, these data suggest that inverted sand dollars are able to recognize flow direction and respond by modifying their orientation to maximize lift and drag for righting.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12009" xmlns="http://purl.org/rss/1.0/"><title>The anus as a second mouth: anal suspension feeding by an oral deposit-feeding sea cucumber</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12009</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The anus as a second mouth: anal suspension feeding by an oral deposit-feeding sea cucumber</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">William. B. Jaeckle, Richard. R. Strathmann</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-29T11:06:20.22416-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12009</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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/">62</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">68</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>Respiratory trees of holothurians are blind-ended evaginations of the posterior digestive system that are rhythmically inflated with seawater via the anus, and are considered to have respiratory and excretory functions. We tested the assimilatory capability of the respiratory tree epithelium by exposing adults of the oral deposit-feeding aspidochirotid sea cucumber <em>Parastichopus californicus</em> to (1) <sup>14</sup>C-labeled unicellular algae and (2) iron-containing macromolecules, and then following the distribution of the labels in various body regions. The abundance of the <sup>14</sup>C (nmol <sup>14</sup>C g wet weight<sup>−1</sup>) varied among body regions. The majority of the label was associated with the respiratory trees. The next greatest concentration was in the rete mirabile of the hemal system. The amount of <sup>14</sup>C within samples of the anterior digestive system, posterior digestive system, and body wall muscle at each sampling time was lower than that of the respiratory trees. The presence and abundance of the <sup>14</sup>C label in samples of the hemal system and the physical association between the respiratory tree and the rete mirabile suggest initial uptake by the respiratory tree and subsequent transfer to the hemal system. The iron label from the protein ferritin and the polysaccharide iron dextran entered cells of the respiratory tree luminal epithelium. The presence of the iron label in mesenchyme cells within the connective tissue compartment of the respiratory trees exposed to ferritin further suggests directional transfer of materials. Holothurians with respiratory trees are nutritionally bipolar; the anus serves as a second mouth.</p></div>
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Respiratory trees of holothurians are blind-ended evaginations of the posterior digestive system that are rhythmically inflated with seawater via the anus, and are considered to have respiratory and excretory functions. We tested the assimilatory capability of the respiratory tree epithelium by exposing adults of the oral deposit-feeding aspidochirotid sea cucumber Parastichopus californicus to (1) 14C-labeled unicellular algae and (2) iron-containing macromolecules, and then following the distribution of the labels in various body regions. The abundance of the 14C (nmol 14C g wet weight−1) varied among body regions. The majority of the label was associated with the respiratory trees. The next greatest concentration was in the rete mirabile of the hemal system. The amount of 14C within samples of the anterior digestive system, posterior digestive system, and body wall muscle at each sampling time was lower than that of the respiratory trees. The presence and abundance of the 14C label in samples of the hemal system and the physical association between the respiratory tree and the rete mirabile suggest initial uptake by the respiratory tree and subsequent transfer to the hemal system. The iron label from the protein ferritin and the polysaccharide iron dextran entered cells of the respiratory tree luminal epithelium. The presence of the iron label in mesenchyme cells within the connective tissue compartment of the respiratory trees exposed to ferritin further suggests directional transfer of materials. Holothurians with respiratory trees are nutritionally bipolar; the anus serves as a second mouth.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12013" xmlns="http://purl.org/rss/1.0/"><title>Growing or reproducing in a temperate sea: optimization of resource allocation in a colonial ascidian</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.12013</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Growing or reproducing in a temperate sea: optimization of resource allocation in a colonial ascidian</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Susanna López-Legentil, Patrick M. Erwin, Marta Velasco, Xavier Turon</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-28T16:10:27.408291-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/ivb.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/ivb.12013</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fivb.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/">69</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">80</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>Relatively little is known about the life cycles of ascidians in temperate seas. Here, we investigated the biological cycle of the colonial ascidian <em>Didemnum fulgens</em>, a dominant species in some shallow localities of the NW Mediterranean Sea. Growth rates and frequencies of fission/fusion events were calculated over a period of 13 months, and the reproductive cycle determined after 32 months of observation. For analyses of reproduction, zooids were dissected in the laboratory and classified into five reproductive categories; these data were used to calculate a maturity index. For growth analyses, underwater photographs of marked colonies were used to estimate the surface area of <em>D. fulgens</em> colonies, calculate monthly growth rates, and document fusion and fission events. Clear seasonal patterns in reproduction and growth were observed, with distinct periods of investment into each function. Gonad maturation started in winter and larval release occurred in early summer, just before maximal sea temperatures were reached. After reproducing, colonies shrank and aestivated during the warmer summer months. Growth occurred during the cooler months, with maximal and minimal growth rates observed in winter and summer, respectively. Fusions and fissions occurred year-round, although fissions were more frequent in fall (coincident with high growth rates) and fusions in spring (coincident with reproduction). These results add to the mounting evidence that ascidian life cycles in temperate seas are characterized by a trade-off between investment in reproduction and growth, triggered by seasonal temperature shifts and constrained by resource availability during summer.</p></div>
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Relatively little is known about the life cycles of ascidians in temperate seas. Here, we investigated the biological cycle of the colonial ascidian Didemnum fulgens, a dominant species in some shallow localities of the NW Mediterranean Sea. Growth rates and frequencies of fission/fusion events were calculated over a period of 13 months, and the reproductive cycle determined after 32 months of observation. For analyses of reproduction, zooids were dissected in the laboratory and classified into five reproductive categories; these data were used to calculate a maturity index. For growth analyses, underwater photographs of marked colonies were used to estimate the surface area of D. fulgens colonies, calculate monthly growth rates, and document fusion and fission events. Clear seasonal patterns in reproduction and growth were observed, with distinct periods of investment into each function. Gonad maturation started in winter and larval release occurred in early summer, just before maximal sea temperatures were reached. After reproducing, colonies shrank and aestivated during the warmer summer months. Growth occurred during the cooler months, with maximal and minimal growth rates observed in winter and summer, respectively. Fusions and fissions occurred year-round, although fissions were more frequent in fall (coincident with high growth rates) and fusions in spring (coincident with reproduction). These results add to the mounting evidence that ascidian life cycles in temperate seas are characterized by a trade-off between investment in reproduction and growth, triggered by seasonal temperature shifts and constrained by resource availability during summer.
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