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Autres Crustacés Autres crustacés Nom scientifique Nom scientifique valide Dénomination Code FAO Date de notification Astacus leptodactylus Ecrevisse à pattes grêles, écrevisse CRD Callinectes sapidus crabe bleu CRB 05/2016 tourteau Jona (sa chair peut être vendue Cancer borealis CRJ comme chair de crabe) tourteau du Pacifique (sa chair peut être Cancer edwardsi CWE vendue comme chair de crabe) 03/2012 tourteau poinclos (sa chair peut être vendue Cancer irroratus CRK comme chair de crabe) crabe tourteau, tourteau (sa chair peut être Cancer pagurus CRE vendue comme chair de crabe) Carcinus maenas crabe vert CRG 05/2016 Cervimunida johni galathée bleue ou galathée ou munida CZJ gérion ouest afticain (sa chair peut être Chaceon maritae CGE vendue comme chair de crabe) Charybdis feriatus crabe nageur, crabe KHF 05/2016 Charybdis natator crabe nageur, crabe KHN 05/2016 Cherax quadricarinatus écrevisse australienne CRP Toutes les espèces du genre crabe des neiges, (la chair peut être vendue - Chionoecetes comme chair de crabe) Homarus americanus Homard américain, homard canadien LBA 09/2014 Homarus gammarus homard, homard européen LBE crabe-crapaud du Canada ou crabe-lyre du Hyas araneus Canada (sa chair peut être vendue comme MVD chair de crabe) crabe-lyre du Canada (sa chair peut être Hyas coarctatus MHV vendue comme chair de crabe) Ibacus ciliatus cigale japonaise, cigale IBC 05/2016 Ibacus novemdentatus cigale japonaise, cigale IBN 05/2016 Jasus edwardsii langouste rouge d'Australie, langouste rouge LOR 05/2016 Jasus frontalis langouste rouge du Chili, langouste rouge LOF 12/2016 Jasus lalandii langouste rouge du Cap, langouste rouge LBC 12/2016 langouste de Saint Paul, langouste australe, Jasus paulensis JSP langouste rouge Jasus tristani langouste de Tristan, langouste rouge LBT 11/2017 Autres crustacés Lithodes aequispina crabe royal brun KAQ 12/2018 Lithodes santolla crabe royal de l’Antarctique KCR 10/2013 Macropipus puber Necora puber étrille LIO Maja squinado araignée de mer SCR Metanephrops andamanicus langoustine andamane NEA 05/2016 Metanephrops challengeri langoustine de Nouvelle Zélande MEC Metanephrops rubellus langoustine d'Uruguay MFS 05/2016 langoustine à raies rouge ou langoustine de Metanephrops thomsoni MFH mer de Chine Nephrops norvegicus langoustine NEP Ovalipes punctatus crabe des sables, crabe OVP 04/2015 Pacifastacus leniusculus écrevisse de Californie, écrevisse signal PCL 07/2019 Palinurus charlestoni langouste du Cap vert, langouste rose NRH 05/2016 Palinurus delagoae langouste de Natal, langouste rose SLN 05/2016 Palinurus gilchristi langouste du Sud, langouste rose SLS 05/2016 Palinurus mauritanicus langouste rose PSL Palinurus vulgaris Palinurus elephas langouste rouge, langouste SLO Panulirus argus langouste blanche, langouste caraïbe SLC 05/2016 Panulirus cygnus Langouste d'Australie LOA Panulirus gracilis langouste verte NUG 05/2016 Panulirus homarus langouste festonnée, langouste tropicale LOK 05/2016 Panulirus interruptus langouste du Mexique, langouste tropicale NUT 05/2016 Panulirus laevicauda langouste indienne, langouste verte NUL 05/2016 Panulirus longipes langouste diablotin, langouste tropicale LOJ 05/2016 Panulirus ornatus langouste ornée, langouste verte NUR 05/2016 Panulirus penicillatus langouste fourchette, langouste tropicale NUP 05/2016 Panulirus polyphagus langouste de vase, langouste verte LMS 05/2016 Panulirus regius langouste royale ou verte LOY Panulirus versicolor langouste bariolée, langouste verte NUV 05/2016 Paralithodes brevipes crabe royal KCY Paralithodes camtschaticus crabe royal, crabe royal du Kamtchatka KCD Paralithodes platypus crabe royal KCI Paralomis granulosa crabe des neiges de l’Antarctique PAG 03/2013 Autres crustacés Platyxanthus orbignyi crabe - 12/2016 Pleuroncodes monodon galathée rouge ou galathée ou munida PQG Pleuroncodes planipes galathée pélagique, galathée LQL Pollicipes pollicipes pouce-pied PCB 03/2013 Toutes les espèces du genre Portunus crabe - 12/2016 Portunus pelagicus crabe SCD Portunus trituberculatus crabe gazami, crabe GAZ 04/2015 Parastacus brasiliensis écrevisse du Brésil TUY Ecrevisse rouge des marais, écrevisse de Procambarus clarkii RCW louisiane Projasus bahamondei langouste chilienne PJH Puerulus angulatus langouste fouet, langouste fouet bandé URL 09/19 Puerulus seweli langouste fouet ou langouste fouet arabe URW Scylla paramamosain crabe de palétuviers, crabe de mangrove YAR Scylla serrata crabe de palétuviers, crabe de mangrove MUD Scylla tranquebarica crabe de palétuviers, crabe de mangrove YAT Scyllarides arctus Scyllarus arctus petite cigale, cigale SCY 12/2016 Scyllarides brasiliensis cigale du Brésil, cigale YLI 12/2018 Scyllarides elisabethae cigale d’Afrique du Sud, cigale YLH 12/2018 Scyllarides herklotsii cigale rouge, cigale YLK 12/2016 Squilla mantis squille, mante de mer, mantis MTS 10/2020 Thenus orientalis cigale raquette, cigale THQ 12/2016 .
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  • Learning in Stomatopod Crustaceans
    International Journal of Comparative Psychology, 2006, 19 , 297-317. Copyright 2006 by the International Society for Comparative Psychology Learning in Stomatopod Crustaceans Thomas W. Cronin University of Maryland Baltimore County, U.S.A. Roy L. Caldwell University of California, Berkeley, U.S.A. Justin Marshall University of Queensland, Australia The stomatopod crustaceans, or mantis shrimps, are marine predators that stalk or ambush prey and that have complex intraspecific communication behavior. Their active lifestyles, means of predation, and intricate displays all require unusual flexibility in interacting with the world around them, imply- ing a well-developed ability to learn. Stomatopods have highly evolved sensory systems, including some of the most specialized visual systems known for any animal group. Some species have been demonstrated to learn how to recognize and use novel, artificial burrows, while others are known to learn how to identify novel prey species and handle them for effective predation. Stomatopods learn the identities of individual competitors and mates, using both chemical and visual cues. Furthermore, stomatopods can be trained for psychophysical examination of their sensory abilities, including dem- onstration of color and polarization vision. These flexible and intelligent invertebrates continue to be attractive subjects for basic research on learning in animals with relatively simple nervous systems. Among the most captivating of all arthropods are the stomatopod crusta- ceans, or mantis shrimps. These marine creatures, unfamiliar to most biologists, are abundant members of shallow marine ecosystems, where they are often the dominant invertebrate predators. Their common name refers to their method of capturing prey using a folded, anterior raptorial appendage that looks superficially like the foreleg of a praying mantis.
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    Molecular Phylogenetics and Evolution 40 (2006) 893–899 www.elsevier.com/locate/ympev Short communication Major rearrangements characterize the mitochondrial genome of the isopod Idotea baltica (Crustacea: Peracarida) Lars Podsiadlowski ¤, Thomas Bartolomaeus Institut für Biologie, Freie Universität Berlin, Germany Received 13 December 2005; revised 11 April 2006; accepted 11 April 2006 Available online 25 April 2006 1. Introduction cies only one euphausiacean and one amphipod species have been sequenced so far. Cladistic analyses of morpho- Mitochondrial genomes represent an important data logical data have led to alternative hypotheses about inter- source for phylogenetic analyses. Thirty-seven genes encod- relationships of living eumalacostracan taxa. The ing for 13 protein subunits, 2 rRNAs and 22 tRNAs are hypotheses of Schram (1986) and Richter and Scholtz usually present in a bilaterian mitochondrial genome (2001) diVer in the position of Decapoda (sister group to (Boore, 1999; Wolstenholme, 1992). Additionally, a non- Euphausiacea or to a clade combining the latter with Per- coding control region can be identiWed in most cases, prob- acarida and Syncarida). Wills (1998) places Syncarida and ably bearing the transcription initiation sites. DiVerent then Peracarida as sister groups to the remainder Eumala- rates of evolutionary change between diVerent parts of the costraca, while other authors favor a basal split between mitochondrial genome make them useful for a variety of Stomatopoda and all other eumalacostracan taxa (Richter phylogenetic questions ranging from studies at the popula- and Scholtz, 2001) or Peracarida and all other Eumalacost- tion level (mitochondrial control region, cytochrome c oxi- raca (Wheeler, 1998). In some studies, peracarids are not dase subunit I and cytochrome b, e.g., Liebers et al., 2004) monophyletic, as Mysidacea (Watling, 1999) do not cluster up to the interrelationships of animal phyla (concatenated with the other peracarid taxa.
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  • Revealed from Complete Mitochondrial Genomes Feng-Jiau Lin1†, Yuan Liu2†, Zhongli Sha2, Ling Ming Tsang3, Ka Hou Chu3, Tin-Yam Chan4, Ruiyu Liu2 and Zhaoxia Cui2*
    Lin et al. BMC Genomics 2012, 13:631 http://www.biomedcentral.com/1471-2164/13/631 RESEARCH ARTICLE Open Access Evolution and phylogeny of the mud shrimps (Crustacea: Decapoda) revealed from complete mitochondrial genomes Feng-Jiau Lin1†, Yuan Liu2†, Zhongli Sha2, Ling Ming Tsang3, Ka Hou Chu3, Tin-Yam Chan4, Ruiyu Liu2 and Zhaoxia Cui2* Abstract Background: The evolutionary history and relationships of the mud shrimps (Crustacea: Decapoda: Gebiidea and Axiidea) are contentious, with previous attempts revealing mixed results. The mud shrimps were once classified in the infraorder Thalassinidea. Recent molecular phylogenetic analyses, however, suggest separation of the group into two individual infraorders, Gebiidea and Axiidea. Mitochondrial (mt) genome sequence and structure can be especially powerful in resolving higher systematic relationships that may offer new insights into the phylogeny of the mud shrimps and the other decapod infraorders, and test the hypothesis of dividing the mud shrimps into two infraorders. Results: We present the complete mitochondrial genome sequences of five mud shrimps, Austinogebia edulis, Upogebia major, Thalassina kelanang (Gebiidea), Nihonotrypaea thermophilus and Neaxius glyptocercus (Axiidea). All five genomes encode a standard set of 13 protein-coding genes, two ribosomal RNA genes, 22 transfer RNA genes and a putative control region. Except for T. kelanang, mud shrimp mitochondrial genomes exhibited rearrangements and novel patterns compared to the pancrustacean ground pattern. Each of the two Gebiidea species (A. edulis and U. major) and two Axiidea species (N. glyptocercus and N. thermophiles) share unique gene order specific to their infraorders and analyses further suggest these two derived gene orders have evolved independently. Phylogenetic analyses based on the concatenated nucleotide and amino acid sequences of 13 protein-coding genes indicate the possible polyphyly of mud shrimps, supporting the division of the group into two infraorders.
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