Podocerus Variegatus Leach, 1814

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Podocerus variegatus Leach, 1814 AphiaID: 103056 ANFÍPODE Animalia (Reino) >Arthropoda (Filo) >Crustacea (Subfilo) >Multicrustacea (Superclasse) >Malacostraca (Classe) >Eumalacostraca (Subclasse) > Peracarida (Superordem) > Amphipoda (Ordem) > Senticaudata (Subordem) > Corophiida (Infraordem) > Caprellidira (Parvordem) > Caprelloidea (Superfamilia) > Podoceridae (Familia) Sinónimos Jassa variegatus Leach, 1814 Jassa variegatus Leach, 1814 Podocerus darwinii (Spence Bate, 1857) Referências additional source Hayward, P.J.; Ryland, J.S. (Ed.). (1990). The marine fauna of the British Isles and North-West Europe: 1. Introduction and protozoans to arthropods. Clarendon Press: Oxford, UK. ISBN 0-19-857356-1. 627 pp. [details] basis of record Bellan-Santini, D.; Costello, M.J. (2001). Amphipoda. in: Costello, M.J. et al. (Ed.) (2001). European register of marine species: a check-list of the marine species in Europe and a bibliography of guides to their identification. Collection Patrimoines Naturels 50: pp. 295-308. [details] original description LEACH W.E. (1814a). Crustaceology The Edinburgh Encyclopedia, 7: 402-404. [details] additional source Bachelet, G.; Dauvin, J.-C.; Sorbe, J.C. (2003). An updated checklist of marine and brackish water Amphipoda (Crustacea: Peracarida) of the southern Bay of Biscay (NE Atlantic). Cah. Biol. Mar. 44(2): 121-151 [details] additional source Leach, W. E. (1816). A tabular view of the external characters of four classes of animals, which Linné arranged under Insecta; with the distribution of the genera composing three of these classes into orders, &c. and descriptions of several new genera and species. Transactions of the Linnean Society of London. 11(2): 306-400., available online at http://biodiversitylibrary.org/page/756873 [details] original description Leach, W.E. (1814). Crustaceology. In: Brewster’s Edinburgh Encyclopaedia. 7: 383-437., available online athttps://www.biodiversitylibrary.org/item/114403#page/431/mode/1up 1 [details] additional source Stebbing, T.R.R. (1888). Report on the Amphipoda collected by H.M.S. Challenger during the years 1873-1876. Report on the Scientific Results of the Voyage of H.M.S. Challenger during the years 1873–76. Zoology. 29 (part 67): i-xxiv, 1-1737, pl. 1-212., available online at http://19thcenturyscience.org/HMSC/HMSC-Reports/Zool-67/htm/doc.html [details] additional source Stebbing T.R.R. (1906). Amphipoda. I. Gammaridea. Das Tiereich. 21, 1-806, 127 figs., available online at http://www.biodiversitylibrary.org/page/998303#page/7/mode/1up [details] Última atualização: 30 Nov. 2017 2.

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The 17Th International Colloquium on Amphipoda
Biodiversity Journal, 2017, 8 (2): 391–394 MONOGRAPH The 17th International Colloquium on Amphipoda Sabrina Lo Brutto1,2,*, Eugenia Schimmenti1 & Davide Iaciofano1 1Dept. STEBICEF, Section of Animal Biology, via Archirafi 18, Palermo, University of Palermo, Italy 2Museum of Zoology “Doderlein”, SIMUA, via Archirafi 16, University of Palermo, Italy *Corresponding author, email: [email protected] th th ABSTRACT The 17 International Colloquium on Amphipoda (17 ICA) has been organized by the University of Palermo (Sicily, Italy), and took place in Trapani, 4-7 September 2017. All the contributions have been published in the present monograph and include a wide range of topics. KEY WORDS International Colloquium on Amphipoda; ICA; Amphipoda. Received 30.04.2017; accepted 31.05.2017; printed 30.06.2017 Proceedings of the 17th International Colloquium on Amphipoda (17th ICA), September 4th-7th 2017, Trapani (Italy) The first International Colloquium on Amphi- Poland, Turkey, Norway, Brazil and Canada within poda was held in Verona in 1969, as a simple meet- the Scientific Committee: ing of specialists interested in the Systematics of Sabrina Lo Brutto (Coordinator) - University of Gammarus and Niphargus. Palermo, Italy Now, after 48 years, the Colloquium reached the Elvira De Matthaeis - University La Sapienza, 17th edition, held at the “Polo Territoriale della Italy Provincia di Trapani”, a site of the University of Felicita Scapini - University of Firenze, Italy Palermo, in Italy; and for the second time in Sicily Alberto Ugolini - University of Firenze, Italy (Lo Brutto et al., 2013). Maria Beatrice Scipione - Stazione Zoologica The Organizing and Scientific Committees were Anton Dohrn, Italy composed by people from different countries.
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Distribución De Los Anfípodos (Crustacea, Malacostraca, Peracarida) De Los Subórdenes Gammaridea, Caprellidea E Hyperiidea, Presentes En El Archipiélago Cubano
Distribución de los anfípodos (crustacea, malacostraca, peracarida) de los subórdenes gammaridea, caprellidea e hyperiidea, presentes en el archipiélago cubano Item Type Journal Contribution Authors Ortiz, M.; Lalana, R. Citation Revista de Investigaciones Marinas, 31 (2), p. 75-90 Download date 27/09/2021 06:30:40 Item License http://creativecommons.org/licenses/by-nc/3.0/ Link to Item http://hdl.handle.net/1834/4520 Rev. Invest. Mar. 31(2):75-90, 2010 DISTRIBUCIÓN DE LOS ANFÍPODOS (CRUSTACEA, MALACOSTRACA, PERACARIDA) DE LOS SUBÓRDENES GAMMARIDEA, CAPRELLIDEA E HYPERIIDEA, PRESENTES EN EL ARCHIPIÉLAGO CUBANO Manuel Ortiz y Rogelio Lalana Centro de Investigaciones Marinas, Universidad de La Habana, Calle 16 No. 114, Playa, CP 11300, Ciudad Habana, Cuba Autor correspondiente: Email: [email protected] RESUMEN Se presenta la distribución espacial y vertical de las 152 especies (37 familias y 83 géneros) de los anfípodos gammarídeos; de las 11 especies (5 familias y 10 géneros) de caprélideos, así como las 36 especies (14 familias y 22 géneros) de hiperídeos, que se han registrado en el Archipiélago Cubano, desde 1970. Cada especie ha sido situada en una tabla que se corresponde con las ecorregiones marinas de Cuba, donde además se ofrece el número de veces que dicha especie ha sido colectada en cada localidad, así como el tipo de sustrato. Palabras clave: distribución de especies; Amphipoda; ASW, Cuba. ABSTRACT The spatial and vertical distribution of the 152 species (37 families and 83 genera) of the gammaridean amphipods; the 11 species (five families, 10 genera)of the caprellidean amphipods, as well as of the 36 species (14 families and 22 genera) of Hyperiidean amphipod crustaceans recorded for the Cuban waters, from 1970, are given.
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(Amphipoda, Podoceridae) Commensal with a Sea Urchin!
A New Species of Dulichia (Amphipoda, Podoceridae) Commensal with a Sea Urchin! L. R. MCCLOSKEy2 THIS REPORT is a description of a new species 6. Inner lobe of maxilla I fringed with 7 of amphipod, Dulicb ia rhabdoplastis n. sp. or 8 setae; inner margin of inner (Gammaridea; Podoceridae) , with observations lobe in maxilla II with long row of on its distribution, behavior, and unique com setae g. X enodice Boeck mensal relationship with the red sea urchin Inner lobe of maxilla I shor t and with Strongylocentrotus [ranciscanus ( Agassiz) . The out setae; inner marg in of inner lobe work was done during a period of postdoctoral of maxilla II with a few bristles support at Friday Harbor Laboratories under · g. N eoxenodice Schellenberg NSF Grant GB-5531. 7. Gnathopods I and II subchelate . ... Tax onom y · g. Podocerus Leach Gurjanova's key (1951, p. 987) to the Podo Gnathopo ds I and II simple . ceridae lists only the three genera found in Rus · g. Icilius Dana sian waters. Stebbing's key (1906, p. 695) does 8. Last pair of uropods normal . not include N eoxenodice Schellenberg. Th ere · g. Dnlicbia Kreyer fore a key to the nine genera in the family is Last pair of uropods rud imentary . included here. · g. Paradulicbi« Boeck KEY TO THE GENERA OF PODOCERIDAE Dnlichia Kroyer, 1845 1. Antenna I without accessory flagellum 2 Body long, slender, cylindrical; first pereo Antenna I with accessory flagellum 4 nite the shortest; sixth and seventh segments 2. Pleon with only five distinct segments fused. Pleon of only five segments-three pleo preceding the telson .
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Table of Contents
TABLE OF CONTENTS Table of Contents.................................................................................................................1 Introduction..........................................................................................................................3 Amphipod Superfamilies.....................................................................................................4 Index of Families.................................................................................................................7 I Suborder Ingolfiellidea....................................................................................................12 Suborder Senticaudata Infraorder Talitrida II. Superfamily Talitroidea........................................................................20 Infraorder Corophiida III. Superfamily Aoroidea.........................................................................65 IV. Superfamily Cheluroidea.....................................................................91 V. Superfamily Chevalioidea....................................................................96 VI. Superfamily Corophioidea.................................................................100 Infraorder Caprellida VII. Superfamily Caprelloidea................................................................142 VIII. Superfamily Neomegamphopoidea................................................191 IX. Superfamily Photoidea......................................................................199 Infraorder Hadziida X.
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Amphipoda Key to Amphipoda Gammaridea
GRBQ188-2777G-CH27[411-693].qxd 5/3/07 05:38 PM Page 545 Techbooks (PPG Quark) Dojiri, M., and J. Sieg, 1997. The Tanaidacea, pp. 181–278. In: J. A. Blake stranded medusae or salps. The Gammaridea (scuds, land- and P. H. Scott, Taxonomic atlas of the benthic fauna of the Santa hoppers, and beachhoppers) (plate 254E) are the most abun- Maria Basin and western Santa Barbara Channel. 11. The Crustacea. dant and familiar amphipods. They occur in pelagic and Part 2 The Isopoda, Cumacea and Tanaidacea. Santa Barbara Museum of Natural History, Santa Barbara, California. benthic habitats of fresh, brackish, and marine waters, the Hatch, M. H. 1947. The Chelifera and Isopoda of Washington and supralittoral fringe of the seashore, and in a few damp terres- adjacent regions. Univ. Wash. Publ. Biol. 10: 155–274. trial habitats and are difficult to overlook. The wormlike, 2- Holdich, D. M., and J. A. Jones. 1983. Tanaids: keys and notes for the mm-long interstitial Ingofiellidea (plate 254D) has not been identification of the species. New York: Cambridge University Press. reported from the eastern Pacific, but they may slip through Howard, A. D. 1952. Molluscan shells occupied by tanaids. Nautilus 65: 74–75. standard sieves and their interstitial habitats are poorly sam- Lang, K. 1950. The genus Pancolus Richardson and some remarks on pled. Paratanais euelpis Barnard (Tanaidacea). Arkiv. for Zool. 1: 357–360. Lang, K. 1956. Neotanaidae nov. fam., with some remarks on the phy- logeny of the Tanaidacea. Arkiv. for Zool. 9: 469–475. Key to Amphipoda Lang, K.
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Author's Personal Copy
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Grandidierella Japonica Class: Multicrustacea, Malacostraca, Eumalacostraca
Phylum: Arthropoda, Crustacea Grandidierella japonica Class: Multicrustacea, Malacostraca, Eumalacostraca Order: Peracarida, Amphipoda, Senticaudata, A brackish water amphipod Corophiida, Corophiidira Family: Aoroidea, Aoridae Description Antenna 1: The first antenna in males Size: Males up to 22 mm in length, females is more than ½ body length (Chapman and 13 mm long (San Francisco Bay, Chapman Dorman 1975) and is much shorter in fe- and Dorman 1975; Myers 1981). The males. The peduncle is with short accessory illustrated specimen (a male, from Coos flagellum in both sexes (Fig. 1b). The male Bay) is 10 mm in length (Fig. 1). flagellum has 20 articles and is a little longer Color: Black head, mottled grey to grey than peduncle. The female flagellum is equal brown body (Chapman and Dorman 1975) to peduncle and consists of 18 articles with distal parts of limbs white (Stephensen (Stephensen 1938). Male antenna one longer 1938; Chapman 2007). This specimen white than its antenna two (Barnard 1973), however (preserved in ETOH). female antennae are of equal size General Morphology: The body of amphi- (Stephensen 1938) (female not figured). pod crustaceans can be divided into three Antenna 2: Length from ¾ of to longer major regions. The cephalon (head) or than antenna one (Chapman and Dorman cephalothorax includes antennules, anten- 1975) (see antenna 1). Spines present on nae, mandibles, maxillae and maxillipeds peduncle articles 3–5. Male second antenna (collectively the mouthparts). Posterior to stout and flagellum with seven articles the cephalon is the pereon (thorax) with (Stephensen 1938). Female second antenna seven pairs of pereopods attached to pere- length in equal to antenna one and fifth article onites followed by the pleon (abdomen) with of peduncle with four strong spines.
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Title STUDIES on MARINE GAMMARIDEAN AMPHIPODA OF
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1 Amphipoda of the Northeast Pacific
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Amphipoda: Senticaudata: Podoceridae
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First Observations of the Behaviour of the Deep-Sea Amphipod Dulichiopsis Dianae Sp
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The distribution of benthic amphipod crustaceans in Indonesian seas Tri Arfianti1 and Mark John Costello2,3 1 Research Center for Biology, Indonesian Institute of Sciences, Cibinong, Jawa Barat, Indonesia 2 School of Environment, University of Auckland, Auckland, New Zealand 3 Faculty of Bioscience and Aquaculture, Nord University, Bodø, Norway ABSTRACT Amphipod crustaceans are an essential component of tropical marine biodiversity. However, their distribution and biogeography have not been analysed in one of the world's largest tropical countries nested in the Coral Triangle, Indonesia. We collected and identified amphipod crustaceans from eight sites in Indonesian waters and combined the results with data from 32 additional sites in the literature. We analysed the geographic distribution of 147 benthic amphipod crustaceans using cluster analysis and the `Bioregions Infomaps' neural network method of biogeographic discrimination. We found five groups of benthic amphipod crustaceans which show relationships with sampling methods, depth, and substrata. Neural network biogeographic analysis indicated there was only one biogeographic region that matched with the global amphipod regions and marine biogeographic realms defined for all marine taxa. There was no support for Wallaces or other lines being marine biogeographic boundaries in the region. Species richness was lower than expected considering the region is within the Coral Triangle. We hypothesise that this low richness might be due to the intense fish predation which may have limited
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