Amphipod newsletter 36 36 ( 2012 ) Facebook and other List of new genera Feature Interview Meetings and info media A list of the new genera of our new Feature starts out with 15th ICA, Poland 2013 Amphipods everywhere! Amphipoda since AN 10 (1970) Wim Vader. Page 58 Page 2 Page 34 Page 55 Palermo 2011. Bibliography Page 59 Page 4 GREETINGS FROM THE EDITORS In addition to the bibliography in this newsletter is a list of the new genera of Amphipoda since AN 10 (1970). One update we hope you will find useful in this Newsletter are direct links to some of the papers (those underlined in blue) in the Bibliography Also included in this Newsletter is a list of new amphipod genera described since AN 10 (1970). This list is provided to you from the hard and loving work of Wim. Thank you Wim! It is also available in excel format. Please look for it on the webpage. New to this Newsletter is a section titled — an Amphipodologist Interview. We have long thought about how to highlight the career and personality of one of your colleagues. To open this segment, we thought it would be most appropriate to interview someone very close to us - Wim Vader. We hope you enjoy this segment. Look for it in future AN’s. And if there is anyone whom you would like us to interview, please send your suggestions to co-editor Adam Baldinger. Reports on recent amphipod conference/meetings are included. And information on upcoming meetings, namely the 15^^ International Colloquium on Amphipoda to be held 2-7 September 2013 in Szczawnica, Poland is provided as well. Also, included is information on the relatively new Amphipod Facebook page. And amphipods have been in news this last year, and co-editor Miranda Lowe tells you more about that. We have promised you a new and updated website/ webpage. Progress is being made, although much slower than expected. If any of you are interested in helping to develop an amphipod webpage /website, please contact Adam Baldinger. We hope you will enjoy Amphipod Newsletter 36! We are very happy to hear from you! Please continue to send us your comments, particularly on how we can make this/your Amphipod Newsletter better. With our best wishes, Wim, Adam, Miranda and Anne Helene 1 Amphipod newsletter 36 J. Amphipods on Facebook ! Murat Ozbek thought it was time to do something about the family-feeling within the amphipod-gang also for the newcomers - and so he started a facebookpage. On January 3 1®*^ 201 2 (facebook is good on keeping track) the page was started, with the comment: “the aim of this is to strengthen friendship between the amphipod workers from all over the world. I hope this will be useful :)” So far (end may 2012) there are 36 members of the group, and more are welcome. Amphipodworkers both new and more seasoned have joined, and people have posted links to their new papers, their cool pictures (or other peoples pictures they really like), have asked questions about literature and practicalities like dissection methods and photography, and posted information and photos of meetings new and old. We promise to post this newsletter there too, of course, and hope more of you readers will see the use and fun of this site. Murat - who started the group How to join: To become a member of the amphipod group on facebook^ pleace go to hffp:// www.facebook.com/groups/ 238356639577927/ and register as a member. Easy! Welcome!! You are invited to share your questions^ papers^ frustrations^ ideas, pictures and thoughts - or just to hang around and see what everybody else is writing/ posting. Find us on Facebook Super giant shrimp deep under cover Its not often we come across such a big amphipod story in the news to say the least, but in February this year a story surfaced about a 28cm (11 in) amphipod! Expedition leader Dr Alan Jamieson (University of Aberdeen's Oceanlab), Dr Ashley Rowden (National Institute of Water and Atmospheric Research, New Zealand) and their team were doing some research in the Kermadec Trench which is one of Earth's deepest oceanic trenches to hnd deep-sea snail hsh using large metal traps encased in sapphire glass to resist the deep ocean high pressures and submergence cameras. Snailhsh had not been seen or photographed since the 1950’s. When the traps emerged back on deck to their great surprise not only the sight of snailhsh caught there attention! There was excitement of seeing the snailhsh again but a few seconds later Dr Jamieson spotted a huge amphipod 28cm (11 in) long - "It's a bit like hnding a foot-long cockroach." he said. From left to right: Toyo Fujii, Alan Jamieson, and Ashley Rowden. Photograph courtesy Oceanlab, University of Aberdeen 2 Amphipod newsletter 36 This was the hst time this amphipod had been observed from the deep trench even though the team had sampled from this area twice before. It was a golden moment to be short lived as a few days later the sampling equipment was deployed again and there was not a single giant amphipod in sight! This amphipod may not be out of the scientihc gaze for too long as one of The Natural History Museum, London researchers is a close collaborator with Dr Jamieson and has promised to enquire about having a specimen for the London collections in the future. Photograph courtesy Oceanlab, University of Aberdeen The average size of most deep water amphipods found elsewhere is usually 2-3 cm although but this super giant amphipod seems to have a size range from 28 cm — 34 cm. Seven specimens were brought up on the ship and nine of the largest size (34cm) were observed on camera only. It is thought that perhaps unusual environmental conditions or the food environment may be the cause of its huge size but there are still lots of questions still to be answered. There is still a lot learn about ocean life in New Zealand's most deep and unique habitat. Perhaps this amphipod is Alicella gigantea as this is the largest species of amphipod ever observed, with some individuals reaching up to 340 millimetres (13 in) long and can be found in deep-waters. Miranda Lowe Department of Life Sciences, The Natural History Museum (NHM), South Kensington, London, UK. Shrimp invasion UK! A new invasive shrimp guide has been written by Michael Dobson (Director, The Freshwater Biological Association) and photos by Miranda Lowe. The shrimp guide is now complete and accessible as a free download from: http:/ / www.fba.org.uk/ downloads Feedback is welcome and if you do have any comments please email these to the author: mdobson@,fba. org.uk . Identffying Invasive F^es^^va!ef Shnmps and Isopods Cofcv:#' 3 Amphipod newsletter 36 BIBLIOGRAPHY 36 (15 IV 2012) AGOSTINO, M., M. MOREIRA- SANTOS & R. RIBEIRO 201 L A freshwater amphipod toxicity test based on postexposure feeding and the population consumption inhibitory concentrations. — Chemosphere, in press. (Test organism was Echinogammarus meridionalis.) AHYONG, S. T. J. K. EOWRY, M. AEONSO, R. N. BAMBER, G. A. BOXSHAEE, P. CASTRO, S. GERKEN, G. S. KARAMAN, J. W. GOY, D. S. JONES, K. MEEAND, D. S. ROGERS &J. SVAVARSSON 2011. Subphylum Crustacea Briinnich, 1772. In: Zhang, Z.-Q (Ed.). Animal biodiversity: An outline of higher- level classihcation and survey of taxonomic richness. — ^ootaxa 3148^ 165-191. AMSEER, G. D., J. B. McGEINTOGK & B. J. BAKER 2012. Amphipods exclude hlamentous algae from the Western Antarctic Peninsula benthos: experimental evidence. — Polar Biology 35, 171-177. (Filamentous algae, transplanted from the intertidal to the subtidal, are rapidly eaten by amphipods) ANDRADE, H. & P. E. RENAUD 2011. Polychaete/ amphipod ratio as an indicator of environmental impact related to offshore oil and gas production along the Norwegian continental shelf — Marine Pollution Bulletin 62, 2836-2844. ANTEAU, M. J. 2011. Do interactions of land use and climate affect productivity of water birds and prairie- pothole wetlands? — Wetlands 32, 1-10. APPY, R. & E. W. BUTTERWORTH 2011. Development of Ascarophis sp. (Nematoda: Cystidicolidae) to maturity in Gammams deubeni (sic) (Amphipoda). — Journal of Parasitology 97, 1035-1048 ARBAGIAUSKAS, K., G. VISINSKIENE & S. SMIEGEVICIENE 2011. Non-indigenous macroinvertebrate species in Eithuanian fresh waters. Part 2. Macroinvertebrate assemblage deviation from naturalness in lotic systems and the consequent potential impacts on ecological quality assessment.. — Knowledge and Management of Aquatic Ecosystems 402-13, 18 pp. (The amphipods Pontogammarus robustoides and Chelicorophium curvispinum had a high impact on Eithuanian lotic systems. Three further amphipods in Table 1) ARIYAMA, H. & K. AZUMA 20 1 1 . A new genus and species of Paracalliopiidae (Crustacea: Amphipoda) from the Shimanto Estuary, western Japan. — Species Diversity 16, 137-147. (Not seen. Macro c alliop e shimantoensis n. gen., n. sp) ARIYAMA. H. & Y. FUJIWARA 2011. First record of Ericthonius megalopus (Sars, 1979) from bathyal Sagami Bay, including synonymization of Ericthonius tolli Briiggen, 1909 with Ericthonius megalopus (Crustacea: Amphipoda: Ischyroceridae). — Journal of Natural History 45, 2795-2814. (The correct name of this amphipod is Ericthonius megalops. WV) ARPONEN, H. & G. BOSTROM 2012. Responses of mobile epifauna to small-scale seagrass patchiness: is fragmentation important? — Hydrobiologia 680, 1-10. (Edge effects may have a more important role than patch size.) ASPIRAS, A. G., R. PRASAD, D. W. FONG, B. B. GAREINI & D. R. ANGEEINI 2012. Parallel reduction in expression of the eye development gene hedgehog in separately derived cave populations of the amphipod Gammarus minus. — Journal of Evolutionary Biology 25, 995-1001. 4 AVERILL. M. 2011. The ‘killer shrimp’ — a new invasive speeies diseovered in the UK. — Dragonfly News 59, 22. (Deals with Dikerogammarus villosus) AYARI, A., D. BOHLI & K. NASRI-AMMAR 2011. Population dynamics and structure of talitrid amphipods from Bizerte sandy beach (North of Tunisia). — Travaux de Hnstitute Scientiflque, Rabat 2011-6, 13-16. AYARI, A. & K. NASRI-AMMAR 2012. Seasonal variation of the endogenous rhythm in two sympatric amphipods: Talitrus saltator and Talorchestia deshayesii from Bizerte beach (Northern Tunisia). — Biological Rhythm Research, in press. DOI: 10. 1080/09291016.201 1.613620 AYARI, A. & K. NASRI-AMMAR 2012. Locomotory rhythm phenology of Talitrus saltator from two geomorphologically different beaches of Tunisia: Bizerte (N. of Tunisia) and Gulf of Gabes (S. of Tunisia). — Biological Rhythm Research 43, 113-123. AZMAN, B. A. R. & B. H. R. OTHMAN 20 12. Two new species of amphipods of the superfamily Aoroidea (Grustacea: Gorophiidea) from the Strait of Malacca, Malaysia, with a description of a new genus. — Z^oloflcal Studies 81, 232-247. (Deals with Grandidierella melakaensis n. sp. (Melaka, Malaysia) and Klebang barnardi n. gen. n. sp. (Unciolidae, also Melaka, Malaysia).) BAGELA-SPYGHALSKA, K., R. A. WATTIER, G. GENTON & T. RIGAUD 2012. Microsporidian disease of the invasive amphipod Dikerogammarus villosus and the potential for its transfer to local invertebrate fauna. — Biological Invasions, in press. (The microsporidian is Cucumispora dikerogammari’, until now it has only been found in pontogammarids.) BACH, E. & I. DAHEEOF 2012. Eocal contamination in relation to population genetic diversity and resilience of an arctic marine amphipod. — Aquatic Toxicology 114/115C, 58-66. (The amphipod is Orchomenella pinguis.) BAIRD, H. P, K. J. MIEEER &J. S. STARK 2012. Genetic population structure in the Antarctic benthos: Insights from the widespread amphipod, Orchomenella franklini — PLoS One7-3, e 34363. (Considerable genetic diversity was revealed.) BAEASHOy Yu. S. 2011. Parasitism and ecological parasitology. — Entomological Review 91, 1216-1223. BARKOy D. V & E. A. KURASHOV 2011. (Sostav pishchi i skorost’ pitanyia Baikal’skogo vselentsa Gmelinoides fasciatus (Stebbing, 1899) v Eadozhskom Ozere.) — Biology a Vnutrennikh Vod 2011-3, 51-61. (In Russian, not seen) BARNES, R. S. K. & M. D. EARNON EEEWOOD 2011. Macrobenthic assemblage structure in a cool-temperate intertidal dwarf eelgrass bed in comparison with those from lower latitudes. — Biological Journal of the Linnean Society 104, 527-540. (The only amphipod is Gammarus locusta) BARTEETT, A. J., ROGHFORT, E. R. BROWN &J. MARSAEEK 2011. Causes of toxicity to Hyalella azteca in a stormwater management facility receiving highway runoff and snowmelt. Part 1 : Polycyclic aromatic hydrocarbons and metals. — Science of the Total Environment 414, 227-237. BARTEETT, A. J., ROGHFORT, E. R. BROWN &J. MARSAEEK 2011. Causes of toxicity to Hyalella azteca in a stormwater management facility receiving highway runoff and snowmelt. Part II: Salts, nutrients, and water quality. — Science of the Total Environment 414, 238-247. BAUZA-RIBOT, M. M., D. JAUME, J. J. FORNOS, G. JUAN &J. PONS 2011. Islands beneath islands: phylogeography of a groundwater amphipod crustacean in the Balearic archipelago. — BMC Evolutionary Biology 2011-11, 1 1 pp. (A study of Metacrangonyx longipes.) 5 BEDINI, R., M. PERTUSATI, E BAToologylSTINI & E. PIAZZI 201 L Spatial and temporal variation of motile maero-invertebrate assemblages assoeiated with Posidonia oceanica meadows. — Acta Adriatic a 52, 201-214. (Amphipods listed on pp 204-205.) BEERMANN, J. & H.-D. FRANKE 201 1. A supplement to the amphipod (Grustaeea) speeies inventory of Helgoland (German Bight, North Sea): indieation of rapid reeent ehange. — Marine Biodiversity Records 4, 15 pp (At least 7 spp are new to the area.) BEERMANN, J. & H.-D. FRANKE 2012. Differenees in resouree utilization and behaviour between eoexisting Jassa speeies (Grustaeea, Amphipoda). — Marine Biology, in press. (Jassa falcata,J. herdmanni andj marmorata on Helgoland.) BEEAIDI, N., A. TAEEB, A. MAHI & G. MESSANA 2011. Gomposition and distribution of stygobionts in the Tafna alluvial aquifer (north-western Algeria). — Subterranean Biology 8 (2010), 21-32. (3 amphipod spp) BERAGKO, P, A. SYKOROVA & A. STANGEER 2012. Life history, seeondary produetion and population dynamies of Gammarus fossarum (Koeh, 1836) in a eonstant temperature stream. — Biologia 67, 164-171. (A Slovakian held study) BERGSMA, G. 2009. Tube-dwelling coral symbionts induce signihcant morphological change in Montipora. — Symbiosis 59 , 143-150. BERGSMA, G. S. 2011. Epibiotic mutualists alter coral susceptibility and response to biotic disturbances through cascading trait-mediated indirect interactions. — Coral Reefs, in press (Amphipods not named, but they change the form of the coral) BERGSMA, G. S. & G. M. MARTINEZ 2011. Mutualist-induced morphological changes enhance growth and survival of corals. — Marine Biology 158, 2261-2211 . (Unidentihed amphipods) BIRDSEY, E. M., E. L. JOHNSTON & A. G. B. POORE 2012. Diversity and cover of a sessile animal assemblage does not predict its associated mobile fauna. — Marine Biology 159, 551-560. (An Australian study.) BLAKESLEE, A. M. H. & A. E. FOWLER 2012 Aquatic introductions and genetic founder effects: How do parasites compare to hosts? — Pp 315-336 in M. Galiskas (Ed.). Analysis of genetic variation in animals. Amazon Digital Services BLOOR, M. G. 2011. Dietary preference of Gammarus pulex wndAsellus aquaticus during a laboratory breeding programme for ecotoxicological studies. — International Journal of fpology 2011, 5 pp BLUHM, B. A., A. V GEBRUK, R. GRADINGER, R. R. HOPGROFT, E HUETMANN, K. N. KOSOBOKOVA, B. I. SIRENKO &J. M. WESLAWSKI 2011. Arctic marine biodiversity. An update of species richness and examples of biodiversity change. — Oceanography 24, 232-248. BLYTHE, M. J., S. MALLA, R. EVERALL, Y. SHIH, V LEMAY, J. MORETON, R. WILSON & A. A. ABOOBAKER 2012. High through-put sequencing of the Parhyale hawaiensis mRNAs and micro RNAs to aid comparative developmental studies. — PLoS One 7-3, e33784. BOETS, P, K. LOGK & P. L. M. GOETHALS 2012. Assessing the importance of alien macro-Grustacea (Malacostraca) within macroinvertebrate assemblages in Belgian coastal harbours. — Helgoland Marine Research, in press BOETS, P, K. LOGK, P. L. M. GOETHALS, G. R. JANSEN & K. A. G. DE SGHAMPHELAERE 2012. A comparison of the short-term toxicity of cadmium to indigenous and alien gammarid species. — Ecotoxicology, in press (The indigenous spp are Gammarus pulex and G. fossarum, the alien spp Dikerogammarus villosus, Echinogammarus berilloni, Gammarus roeseli and G. tigrinus. Large differences between species, but no clear trend. ) 6 BOROWSKY, B. 2011. Responses to light in two eyeless eave dwelling amphipods [Niphargus ictus diivd Niphargus frasassianus). — Journal of Crustacean Biology 3f 613-616. (Both speeies ean detect light and show some negative phototaxis.) BORZA, P. 2011. Revision of invasion history, distributional patterns, and new records of Gorophiidae (Crustacea: Amphipoda) in Hungary. — Acta JpologLca Academiae Scientiarum Hungaricae 57 ^ 75-84. (The oldest records (1917), earlier identihed as Corophium curvispinum^ were in fact C. sowinskyi; C. curvispinum arrived later. Also C. maeoticum (1943 only) and C. robustum (from 2007) have been found.) BOUSLAMA, M. E, F. GHARFI-GHEIKHROUHA, M. EL GTARI, K. NASRI-AMMAR, A. OUESLATI & F. SGAPINI 2011. Relationships between biological characteristics of the crustacean amphipod Talitrus saltator, including behavioural responses, and local environmental features. Case studies of Zouara and Korba (Tunisia). — Travaux de Hnstitute Scientifique, Rabat 2011-6, 17-23. BOYERO, L., L. A. BARMUTA, L. RATNARAYAH, K. SCHMIDT & R. G. PEARSON 2012. Effects of exotic riparian vegetation on leaf breakdown by shredders: a tropical-temperate comparison. — Freshwater Science 31, 296-303. (i.a. Antipodeus wellingtoni in Tasmania.) BRANDT, A. 2012. Southern ocean deep-sea isopod biodiversity research: from census to ecosystem functioning. Pp 21-34 in G. di Prisco & G. Verde (Eds). Adaptation and evolution in marine environments. Volume I. From pole to pole. Springer- Verlag Berlin-Heidelberg. (Also of interest for amphipod workers!) BRANDT, A. & J. GUTT 2011. Biodiversity of a unique environment: the Southern Ocean benthos shaped and threatened by climate change. Pp 503-526 in F. E. Zachos & J. G. Habel (eds). Biodiversity hotspots. Springer- Verlag Berlin Heidelberg. BROOKS, S. J. & C. LLOYD MILLS 2011. Osmoregulation in hypogean population of the freshwater amphipod, Gammarus pulex (L.). — Journal of Crustacean Biology 31, 332-338. BUHL-MORTENSEN, L., P. BUHL-MORTENSEN, M. F. J. DOLAN, J. DANNHEIM, V BELLEG & B. HOLTE 2012. Habitat complexity and bottom fauna composition at different scales on the continental shelf and slope of northern Norway. — Hydrobiologia 685, 191-219 BUNDSCHUH, M., J. P. ZUBROD, D. ENGLERT, F. SEITZ, R. R. ROSENFELDT & R. SCHULZ 2011. Effects of nano-Ti02 in combination with ambient UV-radiation on a leaf shredding amphipod. — Chemosphere 85, 1563-1567. {Gammarus fossarum) BUSGHBAUM, G., D. LACKSCHEWITZ & K. REISE 2012. Nonnative macrobenthos in the Wadden Sea ecosystem. — Ocean & Coastal Management, in press. {Caprella mutica and Gammarus tigrinus the only amphipods treated.) CARDOSO, G. M., A. A. de la P. BUENO & R. L. FERREIRA 201 1. A new troglobitic species of Hyalella (Crustacea, Amphipoda, Dogielinotodae) from Southeastern Brazil. — JVauplius 19, 17-26. {H. spelaea Bueno & Cardoso n. sp.) CARDOSO, G. M., G. MATTOS, G. H. S. GAETANO, T. M. B. GABRINI, L. B. GALHARDO & F. MEIREIS 2012. Effects of environmental gradients on sandy beach macrofauna of a semi-enclosed bay. — Marine Ecology 33, 106-116 CARDOSO, R. S., F. MEIREIS & G. MATTOS 2011. Crustaceans composition in sandy beaches of Sepetiba Bay, Rio de Janeiro, Brazil. — Check List 7-6, 778-781. (Five amphipod species, i.a. Ruffosius fluminensis, in Table 1, p. 780.) 7 CARROLL, M. L. & W. G. AMBROSE 2012. Benthic infaunal community variability on the northern Svalbard shelf — Polar Biology, in press. CARVALHO, S., M. R. GUNHA, E PEREIRA, P. POUSAO-FERREIRA, M. N. SANTOS & M. B. CASPAR 2011. The effect of depth and sediment type on the spatial distribution of shallow soft-bottom amphipods along the southern Portuguese coast. — Helgolarid Marine Research, in press. (Eots of interesting data!) GEVIK, G., E. GAVAS, S. MAVRUK, O. B. DERICI & E GEVIK 2012. Macrobenthic assemblages of newly introduced Caulerpa taxifola from the Eastern Mediterranean coast of Turkey. — Biological Invasions 14: 499-501. Doi: 10.1007/sl0530-01 1-0095-7 (Names of the 31 crustaceans are in the online version - see through the doi.) CHAOUTI, A. & A. BAYED 2011. Categories of importance as a promising approach to valuate and conserve ecosystem integrity: the case study of Asilah sandy beach. — Travaux de ^Institute Scientijique, Rabat 2011-6, 107-110. (Deals i. a. with 5 species of sand-living amphipods) CHENEEOT, H., S. C. JEWETT & M. K. HOBERG 2011. Macrobenthos of the nearshore Aleutian Archipelago, with emphasis on invertebrates associated with Clathromorphum nereostratum (Rhodophyta, Corallinaceae). — Marine Biodiversity 41, 413-424. (Amphipods only identihed to family) GROWN, S. E. 2012. Antarctic marine biodiversity and deep-sea hydrothermal vents. — PLOS Biology 10-1, 1-4. CISNEROS, K. O., A. T. SMIT, J. EAUDIEN & D. S. SCHOEMAN 2011. Complex, dynamic combination of physical, chemical and nutritional variables controls spatio-temporal variation of sandy beach community structure. — PLOS One 6-8, 1 3 pp (A S. African study.) COFFIN, M. R. S. , M. A. BARBEAU & D. J. HAMIETON 2012. Effect of the mud snail Ilyanassa obsoleta on vital rates of the intertidal amphipod Corophium volutator. — Journal of Experimental Marine Biology and Ecology 418-419, 12-23. GOEEMAN, G. O. & E. MATURANA HEINZ 201 1. A new Curidia (Crustacea, Amphipoda, Ochlesidae) from Christmas Island, Australia, Indian Ocean. — fposystematics and Evolution 87, 197-203. [Curidia andreae n. sp.) GONNEELY, T. E., D. DEIBEE & G. G. PARRISH 2011. Elemental composition, total lipid content, and lipid class proportions in zooplankton from the benthic boundary layer of the Beaufort Sea shelf (Canadian Arctic). — Polar Biology , in press (With data on 16 amphipod species) GONEAN K. E., S. E. KIM, A. R. THURBER & E. HENDRYGKS 2010. Benthic changes at McMurdo Station, Antarctica following local sewage treatment and regional iceberg-mediated productivity decline. — Marine Pollution Bulletin 60, 419-432. (Amphipods listed in Appendix 1) CONVEY, P, D. K. A. BARNES, H. J. GRIFFITHS, S. M. GRANT, K. EINSE & D. N. THOMAS 2012. Biogeography and regional classifications of Antarctica. — Chapter 15 in A. D. Rogers, N. M. Johnston, E. J. Murphy & A. Clarke (eds). Antarctic ecosystems: an extreme environment in a changing world. John Wiley & Sons, Etd, Chichester, UK. (Not seen) COOK, K., M. A. VANDERKEIFT & A. G. B. POORE 2011. Strong effects of herbivorous amphipods on epiphyte biomass in a temperate seagrass meadow. — Marine Ecology Progress Series 442, 263-269. (When amphipods were excluded — by a slow-release insecticide — this resulted in a large increase in epiphytic algae in a Posidonia meadow.) GORBARI, E., E. DURAND, M.-A. GAMBON-BONAVITA , E GAEE & Ph. COMPERE 2012. New digestive symbiosis in the hydrothermal vent amphipod Ventiella sulfuris. — Comptes Rendus Biologies, in press (Bacterial communities are present in the midgut and hindgut.) 8 GORDAUX, R., S. PIGHON, H. BEN AFIA HATIRA, V DOUBLET, P. GREVE, L MARGADE, G. BRAQUART-VARNIER, G. SOUTY-GROSSET, E GHARFI-GHEIKHROUHA & D. BOUGHON 2012. Widespread Wolbachia infeedon in terrestrial isopods and other crustaceans. — ^ooKeys 176^ 123-131. (Found in Talitrus saltator in SW France.) GORNET, S. 2012. Density-dependent effects on parasite growth and parasite-induced host immunodepression in the larval helminth Pomphorhynchus laeuis. — Parasitology 138, 257-265. (A parasite of Gammarus pulex.) GORNET, S., G. LUQUET & L. BOLLAGHE 2011. Influence of female moulting status on pairing decisions and size-assortative mating in amphipods. — Journal of Zoology 286, 312-319. (Studies on Gammarus pulex.) GOTHRAN, R. D. , K. GHAPMAN, A. R. STIFF & R. A. RELYEA 2012 “Gryptic” direct benefits of mate choice: choosy females experience reduced predation risk while in precopula. — Behavioural Ecology & Sociobiology, in press. (Studies on two cryptic Hyalella species from Ganada.) GOTHRAN, R. D., A. KUZNIG, G. A. WELLBORN & R. A. RELYEA 2010. Phenotypic manipulation provides insights into the function of a sexually selected trait in a freshwater crustacean species complex. — Animal Behavior 80, 543-549. (Not seen. A study on Hyalella.) GOTHRAN, R. D., A. R. STIFF, P. D. JEYASINGH & R. A. RELYEA 2011. Eutrophication and predation risk interact to affect sexual trait expression and mating success. — Evolution 66, 708-719. (Studies on Hyalella) GOTTIN, D., D. ROUSSEL, N. FOUGREAU, E HERVANT & G. PISGART 2012. Disentangling the effects of local and regional factors on the thermal tolerance of freshwater crustaceans. — Naturwissenschcften 99, 259-264. (A study on Gammarus pulex) GOULAUD, R., O. GEFFARD, B. XUEREB, E. LAGAZE, H. QUEAU, J. GARRIG & A. GHAUMOT 2011. In situ feeding assay with Gammarus fossarum (Grustacea): modelling the influence of confounding factors to improve water quality biomonitoring. — Water Research, in press. GRUZ-RIVERA, E. & M. FRIED LANDER 2011. Feeding preferences of mesograzers on aquacultured Gracilaria and sympatric algae. — Aquaculture 322-323, 218-222. DABRIN, A., G. L. DURAND, J. GARRIG, O. EFEARD, B. J. D. FERRARI & M. GOQUERY 2012. Goupling geochemical and biological approaches to assess the availability of cadmium in freshwater sediment. — Science of the Total Environment, in press. {Gammarus fossarum one of three test animals) DANELIYA, M. E., R. M. KAMALTYNOV «& R. VAINOLA 2011. Phylogeography and systematics of Acanthogammarus s. str., giant amphipod crustaceans from Lake Baikal. — Scripta 40, 623-637. (An important molecular study, with taxonomic consequences, which will apparently be specified elsewhere.) DEGKER, G., M. MORINEAUX, S. VAN GAEVER, J.-G. GAPRAIS, A. LIGHTSGHLAG, O. GAUTHIER, A. G. ANDERSEN & K. OLU 2011. Habitat heterogeneity influences cold-seep macrofaunal communities within and among seeps along the Norwegian margin. Part 1: macrofaunal community structure. — Marine Ecology, in press. (Many amphipods, but not specifically identified.) DOI: 10. 1 1 1 1/j. 1439-0485.201 1.00503.x DEGKER, G. & K. OLU 2011. Habitat heterogeneity influences cold-seep macrofaunal communities within and among seeps along the Norwegian margin. Part 2: contribution of chemosynthesis and nutritional patterns. — Marine Ecology, in DOI: 10. 1 1 1 1/j. 1439-0485.201 1.00486.x DEJUAN, S. &J. E. GARTES 2011. Influence of environmental factors on the dynamics of macrobenthic crustaceans on soft-bottoms of the Ebro Delta continental shelf (Northwestern Mediterranean). — Scientia Marina 75, 691-700 (Amphipods listed on p. 694.) 9 De-la-OSSA-CARRETEROJ. A., Y del PIEAR-RUSO, E GIMENEZ-GASAEDUEROJ. E. SAnGHEZ- EIZASO & J. D. DAUVIN 2011. Sensidvity of amphipods to sewage pollution. — Estuarine, Coastal and Shelf Science 96, 129-138. (The many amphipods are listed in Table 1.) De los RIOS-ESGAEANTE, P. & A. M. EAZGANO 2011 (?). Aquatie Grustaeeans in the Driest Desert on Earth: REports from the Eoa River, Ataeama Desert, Antofagasta Region, Chile. — Global Advances in Biogeography, Ghpt 1 1. 209- 218.. [Hyalella fossamanchini and H. kochi - geographieal table on p 211) DEEGADO, E., E GUERAO & G. RIBERA 2011. Effeets of different salinities on juvenile growth of Gammarus aequicauda (Malaeostraea: Amphipoda). — International Journal of Jpology 2011, 6pp. DEMCHENKO, N. E. 2010. Eeologieal aspeets of the dominant ^imfcivpod Monoporeia affinis (Amphipoda: Pontoporeiidae) in the infralittoral zone on the northeastern eoast of the Sakhalin Island (Sea of Okhotsk). — Jpol. baetica21, 143-149. DEMCHENKO, N. E. & V I. FADEYEV 2011. Composition and distribution of Amphipoda at the North East eoast of Sakhalin Island, Sea of Okhotsk, (translation of russian title). — Isvestia TInro 166, 244-254. (Figure labels in English, else artiele is in Russian.) DEZFUEI, B. S., A. EUI, S. SQUERZANTI, M. EORENZONI & A. P. SHINN 2012. Gonhrmation of the hosts involved in the life eyele of an aeanthoeephalan parasite of Anguilla anguilla (E.) from Eake Piedilueo and its effeets on the reproduetive potential of its amphipod intermediate host. — Parasitolo^cal Research, in press. (The intermediate host is Echinogammarus tibaldii, and infeeted hosts had fewer eggs) DIEEON, M. 2012. Measuring acute toxicity by using Hyalella azteea in an in situ bioassay for oil contamination on the Kalamazoo river. — Senior Individualized Projeet, Kalamazoo College (Not seen) DIONNE, K., R. VERGIEINO, E DUFRESNE, E GHAREES & G. NOZAIS 201 1. No evidenee for temporal variation in a eryptie speeies eommunity of freshwater amphipods of the Hyalella azteea species complex. — Diversity 3, 390-404. (Three sympatric cryptic Hyalella spp in one Quebec lake!) DIXON, M. J. & P. J. SHAW 2011. Watercress and water quality: The effect of phenethyl isothiocyanate on the mating behaviour of Gammarus pulex. — International Journal of Zoology 2011, 9 pp. DO, V T, X. De MONTAUDOUIN, N. EEVESQUE, H. BEANGHET & H. GUYARD 2011. Seagrass colonization: knock-on effects on zoobenthic community, populations and individual health. — Estuarine, Coastal and Shelf Science 95, 458-469. DOBRZYGKA-KRAHEE, A. &J. SUROWIEC 2011. Osmoregulation in Pontogammarus robustoides (G. O. Sars, 1894) (Amphipoda) and its distribution in the brackish waters of northern Poland. — Crustaceana 84, 1755-1767. DOYEE, S. R., E R. MOMO, J.-G. BRETHES & G. A. FERREYRA 2011. Metabolic rate and food availability of the Antarctic amphipod Gondogeneia antarctica (Ghevreux 1906): seasonal variation in allometric scaling and temperature dependence. — Polar Biology 35, 413-424. DROEET, D. 2009. Distribution and movement of the intertidal amphipod Corophium volutator in the upper Bay of Eundy. — PhD Thesis, Univ. of New Brunswick, 200 pp (Not seen) DROEET, D. & M. A. BARBEAU 2012. Population structure of a resident, immigrant and swimming population of Corophium volutator (Amphipoda) on an intertidal mudflat in the Bay of Eundy Canada. — Journal of Sea Research 70, 1-13 lO DROLET, D., T T BRINGLOE, M. R. S. COFFIN, M. A. BARBEAU & DJ. HAMIETON 2012. Potential for between-mudflat movement and metapopulation dynamics in an intertidal burrowing amp bipod. — Marine Ecology Progress Series 449, 197-209. [Corophium volutator.) DUARTE, G., K. ACUNA, J. M. NAVARRO & I. GOMEZ 2011. Intra-plant differences in seaweed nutritional quality and chemical defenses: importance for the feeding behaviour of the intertidal amphipod Orchestoidea tuberculata. — Journal of Sea Research 66, 215-221. DUFOUR, G. 2010. The influence of stranded kelp (Durvillea antarcticaj on the macrofaunal assemblages of a southern New Zealand exposed beach. — M. Sc Thesis, Univ. of Otago, NZ (Not seen) DUFRESNE, E & N. JEFFERY 201 1. A guided tour of large genome size in animals: what we know and where we are heading. — Chromosome Research 19, 925-938. (Earge genome sizes are particularly common in Arctic amphipods.) DUTRA, B. K., R. B. SANTOS, A. A. P. BUENO & G. T. OEIVEIRA 2011. Effects of different diets in the biochemical composition, lipid peroxidation and reproductive traits of Hyalella pleoacuta and Hyalella curvispina. — Animal Biology 61, 349-368. (Not seen) DVORETSKY, A. G. 2011. Epibionts of the great spider crab, Hyas araneus (Einnaeus, 1758), in the Barents Sea. — Polar Biology 35, 625-631. (4 amphipods spp, i.a. Ischyrocerus commensalis, in Table 2) DVORETSKY, A. G. & V G. DVORETSKY 2011. Interspecihc competition of symbiotic and fouling species of red king crab in the Barents Sea. — Doklady Biological Sciences 440, 300-302. (i.a. Ischyrocerus commensalis) DVORETSKY, A. G. & V G. DVORETSKY 2011. Population biology of Ischyrocerus commensalis, a crab-associated amphipod, in the southern Barents Sea: a multi-annual summer study. — Marine Ecology 32, 498-508. ENOCHS, I. G. 2012. Motile cryptofauna associated with live and dead coral substrates: implications for coral mortality and framework erosion. — Marine Biology 159, 709-722. ENVIRONMENTAE PROTECTION AUTHORITY, WE STERN. AUSTRAEIA 20 1 2. T review of subterranean fauna assessment in Western Australia. Discussion Paper. — Environmental Protection Agency, Perth, 66 pp. (not seen) ESQUETE, P, J. MORIERA &J. S. TRONCOSO 2011. Peracarid assemblages of meadows in an estuarine ecosystem (O Grove inlet, NW Iberian peninsula): spatial distribution and seasonal variation. — Helgoland Marine Research 65, 445-455. (Amph. listed on p. 453) EABREGA, J., R. TANTRA, A. AMER, B. STOEPE, J. TOMKINS, T FRY, J. R. EEAD, G. R. TYEER & T GAEEOWAY 2012. Sequestration of zinc from zinc oxide nanoparticles and life cycle effects in the sediment dweller amphipod Corophium volutator. — Environmental Science & Technology 46(2),\ 128-1 135. DOI: 10. 1021/es202570g EANINI, E., G. M. MARGHETTI, A. BAGZEWSKA, K. SZTYBOR & E SGAPINI 2012. Behavioural adaptation to different salinities in the sandhopper Talitrus saltator (Crustacea: Amphipoda): Mediterranean vs Baltic populations. — Marine & Ereshwater Research 63, 275-281. (Not seen) FINSTON, T. E., M. S. JOHNSON, S. M. EBERHARD, J. S. COCKING, J. M. McRAE, S. A. HAESE & B. KNOTT 2011. A new genus and two new species of groundwater paramelitid amphipods from the Pilbara, Western Australia: a combined molecular and morphological approach. — Records of the Western Australian Museum 26, 154-178. (Deals with Maarrka weeliwolli n. gen, n. sp. (Paramelitidae), found in the upper Fortescue River drainage, Pilbara, W. Australia, and M. etheli n sp. from Ethel Greek, Pilbara. Extensive molecular data on, as well as a key to Pilbara Paramelitidae are provided) n FISHER, T T, RJ. LAW, H. S. RUMNEY, M. E KIRBY & C. KELLY 201 L Towards a scheme of toxic equivalency factors (TEFs) for the acute toxicity of PAHs in sediment. — Ecotoxicology and Environmental Safety, 74(8), 2245-2251. {Corophium volutatork test animal) FITZSIMONS, J. A. & M. ANTOS 2011. Ecological notes on the East Gippsland burrowing crayhsh Engaeus orientalis, including burrow structure and associated fauna. — -Australian fpologist 35, 853-857. (Unidentihed amphipod found in the burrows). FORD, A. 2012. Intersexuality in Grustaeea: An environmental issue? — Aquatic Toxicology, 108, 125-129. FORSLUND, H., O. ERIKSSON & L. KAUTSKY 2012. Grazing and geographic range of the Baltic seaweed Eucus radicans (Phaeophyceae). — Marine Biology Research 8, 386-394 (Gammarus spp important grazers.) GALIL, B.S., P. F. GLAK &J. T. CARLTON (eds.) 2011. In the Wrong Place - Alien Marine Grustaeeans: Distribution, Biology and Impacts. Invading Nature. — Springer Series in Invasion Ecology 6. 716 pages, 163 illustrations (87 in colour). ISBN- 10: 9400705905; ISBN- 13: 9789400705906. GALIPAUD, M., Z. GAUTHEY & L. BOLLACHE 2012. Pairing success and sperm reserve of male Gammarus pulex infected by Cyathocephalus truncatus (Gestoda: Spathobothriidae). — Parasitology 138, 1429-1425. GALLARDO, B., M. PAZ ERREA & D. G. ALDRIDGE 2011. Application of bioclimatic models coupled with network analysis for risk assessment of the killer shrimp, Dikerogammarus villosus, in Great Britain. — Biological Invasions, in press. DOI: 10. 1007 /si 0530-01 1-0154-0 GERGS, R., J. GREY & K.-O. ROTHHAUPT 2011. Temporal variation in zebra mussel [Dreissena polymorpha) density structure the benthic food web and community composition on hard substrates in Lake Gonstanee, Germany. — Biological Invasions, 13(12), 2727-2738. GERHARDT, A., M. BLOOR & G. LLOYD MILLS 2011. Gammarus: important taxon in freshwater and marine changing environments. — International Journal of Zoology 2011, 2pp (Introduction to Gammarus issue) GIRIBET, G. & G. D. EDGECOMBE 2012. Reevaluating the arthropod tree of life. — Annual Review of Entomology, 57, 167-186. GIUSTI, A., L. A. SOMMA & L. FERRARI 2012. Cadmium toxieity assessment in juveniles of the austral South America amphipod Hyalella curvispina. — Ecotoxicology and Environmental Safety, 79, 163-169. GISMONDI, E., G. COSSU-LEGUILLE &J.-N. BEISEL 2012. Acanthocephalan parasites: help or burden in gammarid amphipods exposed to cadmium? — Ecotoxicology, 21(4), 1 188-1 193. DOI: 10. 1007/s 10646-0 12-087 3-8 iPolymorphus minutus in Gammarus roeseli', results are different for male and female amphipods.) GISMONDI, E., T. RIGAUD, J.-N. BEISEL & C. GOSSU-LEGUILLE 2012. Microsporidia parasites disrupt the responses to cadmium exposure in a gammarid. — Environmental Pollution 160, 17-23. {Gammarus roeselii) GLADYSHEy M. L, N. N. SUSHCHIK, G. S. KALACHOVA & O. N. MAKHUTOVA 2012. Stable isotope composition of fatty acids in organisms of different trophic levels in the Yenisei River. — PLoS One 7-3, e 34059. (i.a. Eulimnogammarus viridis.) GLAZIER, D. S., E. M. BUTLER, S. A. LOMBARDI , T. J. DEPTOLA, A. J. REESE & E. V SATTERTHWAITE 2011. Ecological effects on metabolic scaling: amphipod responses to hsh predators in freshwater springs. — Ecological Monographs 81, 599-618. (Not seen. Studies on Gammarus minus.) GLAZIER, D. S. & T. J. DEPTOLA 2011. The amphipod Gammarus minus has larger eyes in freshwater springs with numerous hsh predators. — Invertebrate Biology 130, 60-67. 12 GOLDING, L. A., U. BORGMANN & G DUNN 2011. Validation of a chronic dietary cadmium bioaccumulation and toxicity model for Hyalella azteca exposed to field contaminated periphyton and lake water. — Environmental Toxicology and Chemistry, 30(1 1), 2628-2638. GONGALVES, S. G. &J. C. MARQUES 2011. The effects of season and wrack subsidy on the community functioning of exposed sandy beaches. — Estuarine, Coastal and Shelf Science 95, 165-177. (A Portuguese study) GOMEZ, J. & O. DEFEO 2011. Predictive modelling of the sandy-beach supralittoral ?imYthvpod Atlantorchestoidea brasiliensis along a macroscale estuarine gradient. — Estuarine, Coastal and Shelf Science 98, 84-93. GRABOWSKI, M., T. MAMOS, T. REWIGZ, K. BAGELA-SPYCHAESKA & M. OVGHARENKO 2012. Gammarus varsoviensis ]?czdzGwAd, 1975 (Amphipoda, Gammaridae): a long overlooked species in Ukrainian rivers. — North-western Journal of 8, in press. GRABOWSKI, M., T. REWIGZ, K. BACEEA-SPYGHALSKA, A. KONOPACKA, T. MAMOS & K. JAZDZEWSKI 2011. Cryptic invasion of Baltic lowlands by freshwater amphipod of Pontic origin. — Aquatic Invasions 7, in press doi: 10.3391 /ai. 201 2. 7. accepted [Gammarus varsoviensis is a Pontic invader, probably already expanding in the 1 9th century) GREBMAIER, J. M. 2012. Shifting patterns of life in the Pacihc Arctic and sub-arctic seas. — Annual Review of Marine Science 4, 63-75. GUERRA-GARGIA. J. M., M. P. CABEZAS, E. BAEZA-ROJANO &J. G. GARCIA-GOMEZ 2011. Spatial patterns and seasonal fluctuations of intertidal macroalgal assemblages from Tarifa island, southern Spain: relationship with associated Crustacea. — Journal of the Marine Biological Association UK 91, 107-116. GUERRA-GARGIA, J. M., M. P. CABEZAS, E. BAEZA-ROMANO, D. IZQUIERDO, J. CORZO, M. ROS, J. A. SANCHEZ, A. DUGO-GOTA, A. M. FEORES-EEON & M. M. SOEER-HURTADO 20 1 1 . Abundance patterns of macrofauna associated to marine macroalgae along the Iberian penisnula. — Jpologia Baetica 22, 3-17. GUERRA-GARGIA, J. M., M. ROS, A. DUGO-GOTA, V BURGOD, A. M. FLORES-LEON, E. BAEZA- ROJANO, M. P. CABEZAS &J. NUNEZ 2011. Geographical expansion of the invader Caprella scaura (Crustacea: Amphipoda: Gaprellidae) to the East Atlantic coast. — Marine Biology 158, 2617-2622. (Found in SW Spain and on Tenerife , Canary islands.) GUERRA-GARGIA. J. M., M. ROS, D. IZQUIERDO & M. M. SOEER-HURTADO 2012. The invasive Asparagopsis armata versus the native Corallina elongata. Differences in associated peracarid assemblages. — Journal of Experimental Marine Biology & Ecology 416-417, 121-128. GUELSTROM, M., S. BADEN & M. LINDEGARTH 2011. Spatial patterns and environmental correlates in leaf- associated epifaunal assemblages of temperate seagrass [Jpstera marina) meadows. — Marine Biology 159, 413-425. (A Swedish study; Corophium insidiosum and Ericthonius dfformis very abundant) GURKAN, S., T. M. SEVER & E. TASKAVAK 2011. Seasonal food composition and prey-length relationship of pipehsh A7ro/?/zz4 ophidion (Einnaeus, 1758) inhabiting the Aegean Sea. — Acta Adriatica 52, 5-14. (Amphipods are the predominant prey) GUTOW, L., J. D. EONG, O. CERDA, I. A. HINOJOSA, E. ROTHAUSLER, E TALA & M. THIEL 2011. Herbivorous amphipods inhabit protective microhabitats within thaUi of giant kelp Macrocystis pyrifera. — Marine Biology 139, 141-149. (Studies on Peramphithoe femorata in Chile.) HANFLING, B., F. EDWARDS & F. GHERARDI 2011. Invasive alien Crustacea: dispersal, establishment, impact and control. — BioControl 56, 573-595. 13 HANNIBAL, R. L., A. L. PRICE & N. H. PATEL 2011. The functional relationship between ectodermal and mesodermal segmentation on the crustacean, Parhyale hawaiensis. — Developmental Biology, 361, 427-438. HARTKE, T R., G. FISER, J. HOHAGEN, S. KLEBER, R. HARTMANN & S. KOENEMANN 2011. Morphological and molecular analysis of closely related species in the stygobiontic Mphargus (Amphipoda). — Journal of Crustacean Biology 31, 701-709. (On K aquilex, K fontanus, K schellenbergi, K rhenorhodanensis and AC virei) HARTLAND, A., G. D. FENWICK & S. J. BURY 2012. Tracing sewage-derived organic matter into a shallow groundwater food web using stable isotope and fluorescence signature. — Marine & Freshwater Research 62, 1 19-126. (i.a. Paraleptamphopus) HATCHER, M. J., J. T. A. DICK & A. M. DUNN 2012. Diverse effects of parasites in ecosystems: linking interdependent processes. — Frontiers in Ecology and the Environment, 10(4), 186-194. (Not seen) HAUG, C., G. MAYER, V KUTSCHERA, D. WALOSZEK, A. MAAS &J. T. HAUG 2011. Imaging and documenting Gammarideans. — International Journal of fpology 2011-11, 9 pp. (A most useful survey of different methods) HELGOM 2012. Checklist of Baltic Sea Macro-species. Baltic Sea Environmental Proceedings 130. 1-203. HERKUL, K. & J. KOTTA 2009. Effects of eelgrass {fpstera marina) canopy removal and sediment addition on sediment characteristics and benthic communities in the Northern Baltic Sea. — Marine Ecology 30, Suppl. 1, 74-82 HOOP, L. de, A. SGHIPPER, R. LEUVEN, M. HUIJBREGTS, G. H. OLSEN, M. SMIT &J. HENDRIKS 2011. Sensitivity of polar and temperate marine organisms to oil components. — Environmental Science and Technology, in press. HOP, H., G. J. MUNDY, M. GOSSELIN, A. L. ROSSNAGEL & D. G. BARBER 2011. Zooplankton boom and ice amphipod bust below melting sea ice in the Amundsen Gulf, Arctic Canada. — Polar Biology 34, 1947-1958. HOU, Z., B. SKET, G. FISER & S. LI 201 1. Eocene habitat shift from saline to freshwater promoted Tethyan amphipod diversihcation. — Proceedings of the National Academy of Sciences USA 108, 14533-14538. (An important molecular study on 115 species of Gammarus s. 1.) HOWE, P. L. & M. W. CLARK 2011. Toxicity of raw and neutralized bauxite rehnery residue liquors to the freshwater cladoceran Ceriodaphnia dubia and the marine amphipod Paracalliope australis. — Environmental Toxicology, 30(12), 2817-2824. HUNNEKUHL, V S. & G. WOLFF 2012. Reconstruction of cell lineage and spatiotemporal pattern formation of the mesoderm in the amphipod crustacean Orchestia cavimana. — Developmental Dynamics, in press. HYNE, R. V 2011. Review of the reproductive biology of amphipods and their endocrine regulation: identihcation of mechanistic pathways for reproductive toxicants. — Environmental Toxicology and Chemistry, 30(12), 2647-2657. (An important review paper) lANNILLI, V, T. KRAPP & S. RUFFO 2011. Freshwater amphipods from Madagascar with description of a new family, three new genera and six new species (Crustacea, Amphipoda). — Bollettino del Museo Civico di Storia Naturale di Verona, Botanica fpologia 35, 93-137. (Deals with Davidia new genus (In the here erected family Austroniphargidae), with D. spinicaudata n. sp. (Fianarantsoa), Dussartiella aurifex n. sp. (Antananarivo), Libertinia n. gen. (Austroniphargidae) with L. latibasis n. sp. (generotype, Tulear) and L. lonftelson n. sp.(Tulear), Reinhardia n. gen. (Austroniphargidae) , monotypic for R. dimorpha n. sp. (Antsiranana), and Sandro spinidactylus n. sp. (Fianarantsoa). A key to all Madegassan freshwater species is provided, as well as a survey of all reported non-marine species on the island. There is an extensive discussion on the phylogeny and classihcation of the freshwater species of Madagascar; most belong in the 14 here erected family Austroniphargidae; besides the three new genera this family contains the genera Austroniphargus and Sandro. The taxonomic position of Dussartiella remains unclear.) ILARRI, M. L, E FREITAS, S. COSTA-DIAZ, C. ANTUNES, L. GUILHERMINO & R. SOUZA 2012. Associated macrozoobenthos with the invasive Asian clam Corbicula fluminea. — Journal of Sea Research^ in press. (A study from NW Spain) doi: 10. 101 6/j. scares. 201 1.10.0002 ILIFFE, T. M., R. KVITEK, S. BLASCO, K. BLASGO & R. COVILL 2011. Search for Bermuda’s deep water caves. — Hydrobiologia, 677, 157-168. DOI 10. 1007/sl0750-01 1-0883-1 INGELS, J., A. VANREUSEL, A. BRANDT, A. I. GATARINO, B. DAVID, C. DE RIDDER, Ph. DUBOIS, A. J. GOODAY, P. MARTIN, F. PASOTTI & H. ROBERT 2012. Possible effects of global environmental changes on Antarctic benthos: a synthesis across hve major taxa. Ecology and Evolution 2, 453-485. (Not seen, unfortunately. Amphipoda one of the hve taxa.) ITO, A, M. N. AOKI, K. YAHATA & H. WADA 2011. Embryonic development and expression analysis of Distal- less in Caprella scaura (Crustacea, Amphipoda, Gaprellidea). — Biological Bulletin 22 f 206-214. (Not seen) JACKSON, B. P, D. BUGGE,J. F. RANVILLE & C. CHEN 2012. Bioavalability toxicity, and bioaccumulation of quantum dot nanoparticles to the amphipod Leptocheirus plumulosus. — Environmental Science and Technology^ in press DOI: 10.1021/es202864r JACOB, U, A. THIERRY, U. BROSE, W. E. ARNTZ, S. BERG, T. BREY, I. FETZER, T. JONSSON, K. MINTENBECK, C. MOLLMANN, O. L. PETGHEY, J. O. RIEDE &J. A. DUNNE 2011. The role of body size in complex food webs: A cold case. — Advances in Ecological Research 45^ 181-223. (This paper discusses the food web in the Weddell Sea. A species list is found on pp 206-216.) JAMIESON, A. J., A.-N. LORZ, T. FUHI & I. G. PRIEDE 2011. In situ observations of trophic behaviour of Princaxelia amphipods (Crustacea: Pardaliscidae) at hadal depths in four West Pacihc Trenches. — Journal of the Marine Biolof cal Association UK 92, 143-150. (Strong and persistent swimmers, these amphipods, Rjamiesoni, prey on smaller lysianassoids near bait.) JANIAK, D. S. & R. B. WHITLATGH 2012. Epifaunal and algal assemblages associated with the native Chondrus crispus (Stackhouse) and the non-native Grateloupia turuturu (Yamada) in eastern Long Sound. — Journal of Experimental Marine Biology and Ecology 413, 38-44. (Fewer species and individuals in Grateloupia) JAZDZEWSKA, A. & T. KRAPP-SCHICKEL 2011. New data on the distribution of stenothoid amphipods (Crustacea) from Scotia Arc, West Antarctic. — Polish Polar Research 32, 293-320. (With data on Metopoides clavata, M. cf crass a, M. heterostylis, M. lata, M. magellanica, Scaphodactylus carinatus (with Torometopa pseudoperlata as a synonym), S. dentimanus (with Proboloides laevis as a synonym), Torometopa cf antarctica, T. cf crenatipalmatus, ?T macrocheir (with Proboloides nititus as a synonym), Antatelson walkeri, and Prometopa tuberculata. A list of all stenothoids collected is given in Table 1 (pp. 314-315).) JELASSI, R., H. KHEMAISSIA & K. NASRI-AMMAR 2012. Intra-annual variation of the spatiotemporal distribution and abundance of Talitridae and Oniscidea (Crustacea, Peracarida) at Bizerte Lagoon (northern Tunisia). — African Journal of Ecology DOI: 10.1 1 1 1/j. 1365-2028. 2012. 01326.x JONES, D., G. MRABURE & A. GATES 2011. Using industrial remotely operated vehicles in stand-by time for deep-water biodiversity assessment: a case study from offshore Nigeria. — Society of Petroleum Engineers, Annual Technical Conference and Exhibition, Denver, Colorado, Oct.-Nov. 2011. SPE 146439 JOSEFSSON, S., K. LEONARDSSON, J. S. GUNNARSSON & K. WIBERG 2011. Influence of contaminant burial depth on the bioaccumulation of PCBs and PBDEs by two benthic invertebrates [Monoporeia ciffinis and Marenzelleria spp.). — Chemosphere, 85,1444-1451. 15 JOYDAS, T V, M. A. QURBAN, A. AL-SUWAILEM, P. K. KRISHNAKUMAR, Z. NAHEER & N. A. GAEL Macrobenthic community structure in the northern Saudi waters of the Gulf, 14 years after the 1991 oil spill. — Marine Pollution Bulletin 64, 325-335. (Mainly about polychaetes. ‘Oil sensitive amphipods had recolonized the study area.’) JUBEAUX, G., R. SIMON, A. SALVADOR, H. QUEAU, A. GHAMOT & O. GEFEARD 2012. Vitellogenin-like proteins in the freshwater amphipod Gammams fossarum (Koch, 1835): Functional characterization throughout reproductive process, potential for use as an indicator of oocyte quality and endocrine biomarker in males. — Aquatic Toxicology 112/113, 72-82. JUNKER, K., D. SOVILJ, I. KRONGKE &J. W. DIPPNER 2012. Glimate induced changes in benthic macrofauna — ^A non-linear model approach. — Journal of Marine Systems, in press. JUST,J. 2012. Siphonoecetinijust, 1983 (Grustacea, Amphipoda, Ischyroceridae) 9: New species \n Rhinoecetes 1983, Cephaloecetes gen. nov. ?ind Neoecetes gen. nov. from the south-eastern Australian shelf — fpotaxa 3234, 1-42. (Deals with Rhinoecetes robustus, Rh. rhinoceros n. sp. (Pittwater, Sydney, NSW), Rh. dinoceros n. sp. Jervis Bay, NSW), Rh. brevirostris n. sp. (Burwood Beach, NSW), Rh. coclearis n. sp. (E. Bass Strait, Vic.), Rh meridianus n. sp. (Port Phillip Bay, Vic.), Rh. albomaculosus n. sp. Jervis Bay, NSW), Cephalocoetes enigmaticus n. gen. n. sp. Jervis Bay, NSW) Neoecetes conipes n. gen. n. sp.(Port Phillip Bay, Vic.). Key to all the taxa are provided.) KARAMAN, G. S. 2011. Gatalogue: Fauna of Gammaridean Amphipoda (Grustacea, Malacostraca) of the Adriatic Sea. Montenegrin Academy of Sciences and Arts 2, 1-288. (A complete and critical listing of all amphipod records from the Adriatic Sea, an important contribution to our zoogeographic knowledge) KEDRA, M., J. LEGEZYNSKA & W. WALKUSZ 2011. Shallow winter and summer macrofauna in a high Arctic ^ord (79*N, Spitsbergen). — Marine Biodiversity 41, 425-439. (Amphipods listed on p. 437.) KELLY, J. R., R. E. SGHEIBLING & T. BALGH 2011. Invasion-mediated shifts in the macrobenthic assemblage of a rocky subtidal ecosystem. — Marine Ecology Progress Series 437, 69-78. (A studies of changes in Nova Scotia sub tidal ecosystems after sea urchin depredations and invasions of Membranipora and Codium). KENNEDY, K., M. A. BARBEAU & D. DROLET 2011. Winter population dynamics of the intertidal amphipod Corophium^ volutator in the Bay of Fundy. — CGU HS Committee on River Ice Processes and the Environment. 16th Workshop on River Ice, Winnipeg, Sept. 2011., 225-237. KHALAMAN, V V & A. Yu. KOMENDANTOV 2011. Structure of fouling communities formed by Halichondria panicea (Porifera: Demospongiae) in the White Sea. — Russian Journal of Ecology 42, 493-501. (Six amphipod spp in Table 1.) KHAN, E R., N. R. BURY & G. HOGSTRAND 2012. Gopper and zinc detoxihcation in Gammams pulex (L.). — Journal of Experimental Biology 215, 822-832. (Not seen) KI, J.-S., H.-U. DAHM, I.-G. KIM, H. G. PARK, H. HOP & J.-S. LEE 2011. Molecular relationships of gammaridean amphipods from Arctic sea ice. — Polar Biology 34, 1559-1569. (New data on Apherusa glacialis, Gammams wilkitzkii, Onisimus glacialis and 0. nanseni) KILGALLEN, N. M. 2011. New species of Hyalidae (Grustacea, Peracarida, Amphipoda) from New Zealand waters. — New fealand Journal of fpology 38, 251-259. [Apohyale papanuiensis n. sp. (Otago Peninsula, earlier reported as Hyale media), wcid A. freemanae n. sp. (Antipodes islands), with a key to NZ Apohyale) KIM, Y.-H. 2012. Sinocorophium hangangense sp. n. (Grustacea, Amphipoda, Gorophiidae), a new species from Korea, with a key to the genus Sinocorophium. — ZooKeys 181: 53-65. (S. hangangense new species from the Gongreung Stream, Paju-si, Korea; key to all Sinocorophium species and a synoptic table comparing 7 species) 16 KIM, Y-H., E. A. HENDRYCKS & K.-S. EEE 20 IL The genus Guernea Ghevreux, 1887 from Korean waters (Crustacea: Amphipoda: Dexaminidae). — ^ootaxa 3104, 1-25. (Deals with Guernea ezoensis, Gjguensis n. sp. Jejudo Islands), G. namhaensis n. sp. (S. Korean coast) and G. nullispina. A key to N. Pacihc Guernea is provided.) KING, R. A. & R. EEYS 2011. The Australian freshwater amphipods Austrochiltonia australis and Austro chiltonia subtenuis (Amphipoda: Talitroidea: Ghiltoniidae) conhrmed and two new cryptic Tasmanian species revealed using a combined molecular and morphological approach.) — Invertebrate Systematics 25, 171-196. (This nice study deals with Au. australis, Au. clydensis n. sp. (Clyde river, Tasmania), Au. cooperi n. sp. (Take Petrarch, Tasmania) and Au. subtenuis, for which taxon a neotype is established. A key to known Australian chiltoniids is provided.) KNOX, M. A., I. D. HOGG, G. A. PIEDITGH, A.-N. EORZ & S. D. NODDER 2012. Abundance and diversity of epibenthic amphipods (Crustacea) from contrasting bathyal habitats. — Deep Sea Research 1 62, 1-9 KOBAK, J., M. POZNANSKA & T. KAKAREKO 2012. Behavioural changes of zebra mussel Dreissena polymorpha (Bivalvia) induced by Ponto-Gaspian gammarids. — Biological Invasions, in press. DOI: 10. 1007/s 10530-01 2-0 197-x KOBAYASHI, S., T. GOMI, R. C. SID EE &J. N. NEGISHI 2012. Distribution of amphipods [Gammams nipponensis Ueno) among mountain headwater streams with different legacies of debris flow occurrence. — Ecohydrology, in press. DOI: 10.1002/eco.l249 KOEHEER, A. V, Y P. SPRINGER, H. S. RANDHAVA, T. E. E EEUNG, D. B. KEENEY & R. POUEIN 2011. Genetic and phenotypic influences on clone-level success and host specialization in a generalist parasite. — Journal of Evolutionary Biology, on line. (The trematode Maritrema novaezealandensis is a general parasite of N. Zealand amphipods and decapods.-) KOEHEER, E van ARSDAEE 2011. Genetics and ecology of host specificity in the trematode parasite Maritrema novaezealandensis. — Doctoral Thesis, Univ. of Otago, NZ (Not seen. The hosts are Paracalliope novizealancliae and Heterophoxus Stephens eni.) KOKON, M. G. H. &J. GRAEE 2011. Easier detection of invertebrate ”identiflcation-key characters” with light of different wavelengths. — Erontiers in fpology 8/X/21 . (Deep blue or ultraviolet light makes many features much easier to see.) KOPEOVITS, G. &J. B. McGEINTOGK 2011. An evaluation of chemical and physical defenses against flsh predation in a suite of seagrass-associated ascidians. — Journal of Experimental Marine Biology and Ecology 407, 48-53. KOPPEN, K. & C. O. COEEMAN 2011. Seba henriki, a new amphipod (Crustacea, Sebidae) from Norfolk Island, Australia. — fposystematics and Evolution 87, 319-326. KORNOBIS, E. & S. PAESSON 2011. Discordance in variation of the ITS region and the mitochondrial GOI gene in the subterranean amphipod Crangonyx islandicus. — Journal of Molecular Ecology 73, 34-44. KORNOBIS, E., S. PAESSON &J. SVAVARSSON 2012. Glassiflcation of Crangonyx islandicus (Amphipoda, Grangonyctidae) based on morphological characters and comparison with molecular phylogenies. — Jpotaxa 3233, 52-66. KRAFT, A., E. BAUERNFEIND & E.-M. NOTHIG 2011. Amphipod abundance in sediment trap samples at the long-term observatory HAUSGARTEN (Fram Strait, ~79'^N/4'^E). Variability in species community patterns. — Marine Biodiversity 41, 353-364. (Nine pelagic amphipod spp listed on p. 357, with Themisto spp dominant.) KRAFT, A., E. BAUERNFEIND & E.-M. NOTHIG 2011. Size structure and life cycle patterns of dominant pelagic amphipods collected as swimmers in sediment traps in the eastern Fram Strait. — Journal of Marine Systems, 95, 1-15. 17 KRAPP- SCHICKEL, T 2011. New Antarctic stenothoids sensu lato (Amphipoda, Crustacea). — European Journal of Taxonomy 2, 1-17. (Deals with Prometopa cedrici n. sp. (Larsen B area), with key to Prometopa, Antatelson walkeri, and A. claudei n. sp. (Shag Rocks), with key to Antatelson.) KRAPP-SCHICKEL, T. & H.-G. MULLER 2011. Known and unknown hadzioidean amphipods from Polynesia with Elasmopus polynesus sp. nov. and Kairos segregans gen. nov., sp. nov.. — Marine Biodiversity Records 4, 1 1 pp. (Deals with Elasmopus alalo, E. hawaiensis, E. hooheno, E. polynesus n. sp. (Bora Bora) and Kairos segregans n. gen, n. sp. (Carangoliopsidae; Bora Bora).) KREBES, L., M. BLANK & R. BASTROP 2011. Phylogeography historical demography and postglacial colonization routes of two amphi-Atlantic distributed amphipods. — Systematics and Biogeography 9, 259-273. (The species concerned are Gammarus duebeni and G. oceanicus. ) KRONCKE, L, H. REISS, J. D. EGGLETON, J. ALDRIDGE, M. J. N. BERGMAN, S. COCHRANE, J. A. CRAEYMEERSCH, S. DEGRAER, N. DESROY, J.-M. DEWARUMEZ, G. C. A. DUINEVELD, K. ESSINK, H. HILLEWAERT, M. S. S. LAVALEYE, A. MOLL, S. NEHRING, R. NEWELL, E. OUG, T. POHLMANN, E. RACHOR, M. ROBERTSON, H. RUMOHR, M. SCHRATZBERGER, R. WMITH, E. VANDEN BERGHE, J. van DALFSEN, G. van HOEY, M. VINCX, W. WILLEMS & H. L. REES 2011. Changes in North Sea macrofauna communities and species distribution between 1986 and 2000. — Estuarine, Coastal and Shelf Science 94, 1-15. KRONENBERGER, K., C. DICKO & E VOLLRATH 201 1. A novel marine silk. — Naturwissenschaften 99, 3-10. (Describes and analyzes the amphipod silk from Crassicorophium bonellii.) KRONENBERGER, K., P. G. MOORE, K. HALCROW & E VOLLRATH 2012. Spinning a marine silk for the purpose of tube-building. — Journal of Crustacean Biology 32, 191-202. [Crassicorophium bonellii and Lembos websteri.) LA PORTA, B., M. TARGUI, L. LATTANZI, P. LA VALLE, D. PAGNETTI & L. NICOLETTI 2009. Relict sand dredging for beach nourishment in the central Tyrrhenian Sea (Italy): effects on benthic assemblages. — Marine Ecology 30, Suppl. 1, 97-104. (Many amphipods listed on p. 100.) LACERDA, M. B. & S. MASUNARI 2011. (Identihcation key for caprellids (Crustacea, Amphipoda) from the coast of Parana and Santa Catarina states). — Biota Neotropica 1T3, 12 pp. (In Portuguese, covering 10 species.) LACERDA, M. B., I. TAKEUCHI & S. MASUNARI 2011. Redescription of the rare amphipod crustacean Pseudaeginella montoucheti (Quitete, 1971) from Brazil. — JpoKeys 146. 1-17. (With a key to all Pseudaeginella) LALONDE, B. A. & W. ERNST 2012. Analysis of benthic invertebrate communities as a function of distance from two hsh-processing plant effluent discharges in New Brunswick, Canada. — Archives of Environmental Contamination and Toxicology, in press. DOI 10. 1007 /s00244-0 12-9749-4 LANNIN, R. & K. HOVEL 2011. Variable prey density modihes the effects of seagrass structure on predator-prey interactions. — Marine Ecology Progress Series 442, 59-70. LARSEN, M. H., K. T. JENSEN & K. N. MOURITZEN 2011. Climate influences parasite-mediated competitive release. — Parasitology 138(11), 1436-1441. (Data on Corophium arenarium and C. volutator.) LARSEN, P. E 2012. The macroinvertebrate fauna of rockweed [Ascophyllum nodosurr^-dornmvit^d low-energy rocky shores of the northern Gulf of Maine. — Journal of Coastal Research 28, 36-42. LAUDIEN, J. &J.-B. ORCHARD, 2012. The signiflcance of depth and substratum incline for the structure of a hard bottom sublittoral community in glacial Kongs^orden (Svalbard, Arctic) — an underwater imagery approach. — Polar Biology , in press. DOI 10. 1007 /s003000-00 1-1 153-4 18 LAWSON HANDLEY, L.-J., A. ESTOUP, D. M. EVANS, C. E. THOMAS, E. EOMBAERT, B. FACON, A. AEBI & H. E. ROY 2011. Ecological genetics of invasive alien species. — BioControl 56, 409-428. EAZO-WASEM, E. A., T. PINOU, A. PENA DE NIZ & A. FEUERSTEIN 2011. Epibionts associated with nesting marine turtles Lepidochelys olivacea and Chelonia mydas in Jalisco, Mexico: A review and field guide. — Bulletin of the Peabody Museum, of Natural History, 52(2), 221-240. [Podocerus chelonophilus and other turtle epibionts; nice images) EEEVES, S. A. 2011. Bioaccumulation of arsenic, cadmium, mercury, lead and selenium in the benthic arid pelagic food chain of Lake Baikal. — M Sc Thesis, Norwegian University of Science and Technology. (Not seen) EEGEZYNSKA, J., M. KEDRA & W. WAEKUSZ 2012. When season does not matter: summer and winter trophic ecology of Arctic amphipods. — Hydrobiologia 684, 189-214. (‘In general, amphipods feeding habits appeared to be independent of the seasonal phytodetrital pulses.’) El, M. 2011. Interactive effects of phosphorus and copper on Hyalella azteca and periphyton. — M Sc Thesis, Univ. of Michigan, 40pp. EIM, J. H. C. & I. TAKEUGHI 2012. The distinctive species characteristics of Metaprotella sandalensis Mayer, 1898 (Crustacea: Amphipoda), commonly distributed throughout the tropical west Pacihc coasts. — The Raffles Bulletin of fpology 60, 23-34. (This redescription of topotypic material shows that Af. sandalensis auct. probably is a species complex.) EIZOTTE, R. E., E D. SHIEEDS, J. N. MURDOCK & S. S. KNIGHT 2012. Responses of Hyalella azteca and phytoplankton to a simulated agricultural runoff event in a managed backwater wetland. — Chemosphere 87, 684-691. EORZ, A.-N. 2012. First records of Epimeriidae and Iphimediidae (Crustacea, Amphipoda) from Macquarie Ridge, with description of a new species and its juveniles. — fpotaxa 3200, 49-60 (Deals with Epimeria ashleyi n. sp. (Hjort Seamount, Macquarie Ridge, 1 580m) and Labriphimedia pulchridentata, earlier only known from off Heard Island.) EORZ, A.-N., K. EINSE, P. j. smith & D. STEINKE 2012. First molecular evidence for underestimated biodiversity of Rhachotropis (Crustacea, Amphipoda), with description of a new species. — PLoS One 7 (3), e 32365. (The new species is Rh. novazealandica from the Chatham Rise, NZ. The study suggests the presence of further cryptic species in the New Zealand area.) EORZ, A.-N., P. SMITH, K. EINSE & D. STEINKE 2011. High genetic diversity within Epimeria georgiana (Amphipoda) from the southern Scotia Arc. — Marine Biodiversity, in press. ( DNA barcoding revealed 4 clades among E. georgiana s.l. material, three of which are morphologically indistinguishable. The fourth is here described as E. angelikae n. sp. (off Kap Norvegia, E. Weddell Sea).) EOWRY, J. K. & H. E. STODDART 2012. The Pachynidae fam. Nov. (Crustacea: Amphipoda: Eysianassoidea). — fpotaxa 2146, 1-69. (This is a monograph over this family, which here for the hrst time is erected officially. It consists of the following taxa, which almost all are described and illustrated here: Acheronia pegasus, Coriolisa novae aledonia, Drummondia corinellae, D. luce n. sp.(Golfo Gorcovado, Chile), D. marlo n. sp.( Bass Strait, Vic.), D. parviramus, D. tridentata n. sp. (Point Hicks, Vic.), Ekelofia eltanin n. sp. (Ross Sea, 76'^02’S, 179"^57’W), E. oculata, Eigorella angulosa n. sp. (E. of Merimbula, NSW, 1600m), E corindon, E formosa n. sp. (E. of Nowra, NSW), E franklin n. sp. (NE of Twofold bay, NSW, 1000m j, E macrophoculata, E tanidea, E tasmanica, Pachychelium davidis, P fucaense n. sp. Juan de Fuca Strait, BG, Canada). P tropicale n. sp. (off Flynn Reef, Qld, 1000m), Pachynus barnardi, P chelatum, P denticulatum, P obsolescens n. sp. ( Bass Strait, Tasm.) , P puflator, Prachynella epa n. sp. (SW of San Francisco, Calif, 2010m), P lodo, P mediterranea, P. oculata n. sp. (32’^31’N, 1 17"^15’W, Calif), P shijiki n. sp. (W. Kyushu, Japan), Renella n. gen, monotypic, ^ov Drummondia sculptidentata , Sheardella kapala, S. tangaroa, Smaraldia n. g&n.forS. springthorpei n. sp.( Torbay Bay, W. Austr.), and Ultimachelium n. gen., with as type species U. tac n. sp.(Golfo de Ancud, Chile), and as further species U. barnardi and U. nichollsi, both transferred from Pachychelium. Keys to all taxa are provided.) 19 LOWRY, J. K. & H. E. STODDART 2012. Australian and South African conicostomatine amphipods (Amphipoda: Lysianassoidea; Lysianassidae: Gonicostomatinae subfam.nov.). — ^ootaxa 3248: 43-65. (Deals with the subfamily Conicostomatinae, here hnally formally erected, with a key to the 6 genera, and keys to all species.The genus Amphorites n. gen. is erected , with Stomacontion pungapunga as type, and further species yS. hurleyi ^ndAmphorites annasona n. sp. (Middleton Reef, Tasman Sea); Conicostoma carta is redescribed, and in Ocosingo there is also a new species, 0. yatala n. sp. (King Island, Bass str.). Finally, there are 3 new spp in Scopolostoma (which is a neutral noun).* S. darwinense n. sp. (Darwin, NT) , S. keurboomstrandense n. sp. (Port Elizabeth, S. Africa), the latter earlier recorded by Griffiths as S. prionoplax)^ and S. norah n. sp. (Norah Head, NSW. ).) EYUBINA, O. S., O. E. ZIMINA & N. A. ANISIMOVA 2012. Distribution and variation of the amphipod fauna (Grustacea, Amphipoda) in the Kola section (Barents Sea). — Doklady Biological Sciences 442, 27-30. MAGDONAED, E. G., M. G. GINN & D. J. HAMIETON 2012. Variability in foraging behaviour and implications for diet breadth among Semipalmated sandpipiers staging in the Upper Bay of Fundy. — The Condor 114, 135-144. (The birds feed mainly on Corophium volutator.) MAGDONAED, T A., B. J. BURD, V I. MAGDONAED & A. VAN ROODSEEAAR 2010. Taxonomic and feeding guild classihcation for the marine benthic macroinvertebrates of the Strait of Georgia, British Golumbia. — Canadian Technical Report of Fisheries and Aquatic Sciences 2874, iv + 63 p. (amphipod species abundance and biomass, in part used to establish large-scale picture of biota in the Strait of Georgia) MacNEIE, G., &J. T A. DIGK, 2011. Differential predatory and interference interactions between native and invasive freshwater amphipods and a co-occurring mysid (Grustacea). — Hydrobiologia 683, 35-42. [Gammams duebeni celticus, G. tigrinus, Crangonyx pseudogracilis ?aidMysis relicta in Eough Neigh, Ireland) MAITY, S., A. JANNASGH, J. ADAMEG, M. GRIBSKOV, T. NAEEPA, T O. HOOK & M. S. SEPUEVEDA 2012. Metabolite prohles in starved spp. Using liquid chromatography. mass spectrometry (Ec-Ms) based metabolomics. — Journal of Crustacean Biology 3 2 , 239-248. MAITY, S, A. JANNASGH, J. ADAMEG, T NAEEPA, T. O. HOOK & M. S. SEPUEVEDA 2012. Starvation causes disturbance in amino acid and fatty acid metabolism in Diporeia. — Comparative Biochemistry and Physiology B, 161, 348-355. MAEHI, G. S. 2012. The chronic toxicity of titanium dioxide nanoparticles to the freshwater amphipod Hyalella azteca. — M.Sc Thesis, Wilfred Eaurier University, Ganada. (Not seen) MANGINEEEI, G. 2012. On the trophic ecology of Gammaridea (Grustacea: Amphipoda) in coastal waters: A European-scale analysis of stable isotope data. — Estuarine, Coastal and Shelf Science, in press DOI: 10. 10 16/j.ecss.201 1.12.003. MANGINEEEI, G. 2012. To bite, or not to bite? A quantitative comparison of foraging strategies among three brackish crustaceans feeding on leaf litters. — Estuarine, Coastal & Shelf Science, in press DOI.org/ 10. 101 6/j.ecss. 2012.04.002. (One of the three is Gammams aequicauda.) MARIA, T. E, M. DE TROGH, J. VANAVERBEKE, A. M. ESTEVES & A. VANREUSEE 2011. Use of benthic vs planktonic organic matter by beach organisms: A food tracing experiment with 13G labelled diatoms. — Journal of Experimental Marine Biology and Ecology 407, 309-314. (i.a. Bathyporeia pilosa andR sarsi.) MARIN, I. & S. SINEENIKOV Metopelloides paguri sp. nov, a new species of symbiotic stenothoid amphipod (Grustacea; Amphipoda: Stenothoidae) associated with sublittoral hermit crabs from the Russian coast of the Sea of Japan. — Jpotaxa 3244, 59-67. (This new species was discovered on the hermit crab Pagurus pectinatus occupying sponges Suberites sp at Iturup, S. Kurile Islands.) 20 MATS, V D., D. Yu. SHCHERBAKOV & I. M. EFIMOVA 201 L Fate Cretaceous-Cenozoic history of the Fake Baikal depression and formation of its unique biodiversity — Stratigraphy and Geological Correlation 19, 404-421. (This most interesting paper contains i.a. a phylogenetic tree of Baikalian amphipods, superimposed on a time-scale.) MAYEN-ESTRADA, R. & R. AGUIEAR-AGUIEAR 2011. Track analysis and geographic distribution of some Lagenophrys Stein, 1952 (Protozoa: Giliophora: Peritrichia) species. — Journal of Natural History, 46 (3-4), 249-263. [L ampulla and L. nassa recorded on species of Gammaridae.) MAYER, G., A. MAAS & D. WAEOSZEK 2012. Mouthpart morphology of three sympatric native and nonnative gammaridean species: Gammarus pulex, G. fossarum, 3.nd Echinogammarus berilloni (Crustacea: Amphipoda). — International Journal of Zoology (2012), art. ID 493420, 23 pp. MEAD, A.,J. T. GARETON, G. E. GRIFFITHS & M. RIUS 2011. Introduced and cryptogenic marine and estuarine species of South Africa. — Journal of Natural History 45, 2463-2524. (1 1 amphipod spp listed on p. 2467 and discussed on pp 2484-2489.) MEDOC, V, T. RIGAUD, S. MOTRUEIE, M.-J. PERROT-MINOT & E. BOEEAGHE 2011. Paratenic hosts as regular transmission route in the acanthocephalan Pomphorhynchus laevis: potential implications for food webs. — Naturwissenschaften, 98 (10), 825-835. DOI: 10.1007/s001 14-01 10083 1-y. (This freshwater parasite uses amphipods as intermediate hosts; parasitized amphipods contribute to the transmission to a dehnitive host, small- sized hsh). MIRZAJANI, A., M. SAYAD RAHIM & A. SARI 2011. Reproductive traits of some amphipods (Crustacea: Peracarida) in different habitats of Iran and Southern Caspian Sea. — International Journal of Zoology (2011), 10 pp (Data on Gammarus lacustris, G. paricrenatus, G. komareki, G. aequicauda, Obesogammarus acuminatus, Pontogammarus maeoticus and P borceae.) MITGHEEE, R. J., A. E. MYERS, S. A. MABURY, K. R. SOEOMON & P. K. SIBEEY 2011. Toxicity of fluorotelomer carboxylic acids to the algae Pseudokirchnerietta subcapitata and Chlorella vulgaris, and the amphipod Hyalella azteca. — Ecotoxicology and Environmental Safety , 74(8), 2260-2267. MOENIGKES, S., A.-K. SCHNEIDER, E. MUHEE, E. ROHE, O. RICHTER & E SUHEING 2011. From population-level effects to individual response: modelling temperature dependence in Gammarus pulex. — Journal of Experimental Biology 214, 3678-3687. MOISEENKO, T. I. & A. N. SHAROV 2011. Modihcation of water ecosystems during and after the reduction of anthropogenic pollution. — Doklady Biological Sciences 441, 389-392. (Predominant zoobenthos of Fakes Eadoga, Onega and Imandra (northern European Russia) includes Monoporeia ajfnis, M. relicta and Pallasiola quadrispinosa.) MOEDOVAN, O. T, E. EEVEE, C. MARIN, M. BANGIU, H. E. BANCIU, C. PAVEEESGU, T. BRAD, M. CIMPEAN, I. MEEEG, S. lEPURE & I. POVARA 2011. Spatial distribution patterns of the hyporheic invertebrate communities in a polluted river in Romania. — Hydrobiologia 669, 63-82. (study includes Bogidiella sp. Niphargus romanicus and N transsylvanicus) MOEDOVAN, O. T, I.-N. MEEEG & A. PERSOIU 2011. Habitat fragmentation and its effects on groundwater populations. — Ecohydrology, in press. DOI: 10. 1002/ eco.237. {Niphargus andropus within samples from Ciur Izbuc Cave in northwestern Romania.) MORTON, B. & G. N. W. FEE 2011. The composition and spatial distribution of scavenging hyperbenthos in the Gape d’Aguilar Marine Reserve, Hong Kong. — Journal of the Marine Biological Association UK 92, 39-47. (Traps in very shallow water. Ceradocus sp. by far the most common amphipod (see Table 1, p. 41), but this species was even more common in unbaited traps.) MOSER, M. E. & D. S. FEE 2012. Foraging over Sargassum by western North Atlantic seabirds. — The Wilson Journal of Ornithology 124, 66-72. 21 MYERS, A.A., G. RIGOLET, E. THIEBAUT & S. E DUBOIS 2012. A new species of amphipod, Photis inornatus sp. nov. (Gorophiidea, Photidae) from a 'Haploops community’ in Brittany — ^ootaxa 3236, 55-61. (With a key to European Photis species.) NAHAVANDI, N., M. PEATH, R. TIEDEMANN & A. R. MIRZAJANI 2011. Sexual and natural selection on morphological traits in a marine amphipod, Pontogammarus maeoticus (Sowinsky 1894). — Marine Biology Research 7, 135-146. (sexually dimorphic traits in four populations of P maeoticus were studied.) NAVARRO-BARANGO, G., J. M. GUERRA-GARGIA, E. SANGHEZ-TOGINO &J. G. GARGIA-GOMEZ 2012. Soft-bottom assemblages in Mediterranean marine caves: the cave of Gerro Gordo (Granada, Spain) as case study. — Helgoland Marine Research, in press NEFF, J. M. & G. S. DUREEE 2011. Bioaccumulation of petroleum hydrocarbons in Arctic amphipods in the oil development area of the Alaskan Beaufort Sea. — Integrated Environment Assessment and Management, 8(2), 301-319. (study animal is Anonyx nugax) NGUYEN, E. T. H. , B. T. A. MUYSSEN & G. R. JANSSEN 2011. Single versus combined exposure of Hyalella azteca to zinc-contaminated sediment and food. — Chemosphere, 87(1), 84-90. NORDERHAUG, K. M. & H. GHRISTIE 2011. Secondary production in a Laminaria hyperborea kelp forest and variation according to wave exposure. — Estuarine, Coastal and Shelf Science 95, 135-144. NORDERHAUG, K. M., H. GHRISTIE , G. SOGN ANDERSEN & T. BEKKBY 2012. Does the diversity of kelp forest macrofauna increase with wave exposure? — Journal of Sea Research 69, 36-42. (Yes, it does!) NOYON, M., E NARGY, S. GASPARINI & P. MAYZAUD 2012. Ontogenic variations in fatty acid and alcohol composition of the pelagic amphipod Themisto libellula in Kongs^orden (Svalbard). — Marine Biology, 159, 805-816. NUNEZ-PONS, E., M. GARBONE, D. PARIS, D. MEEGK, P. RIOS, J. GRISTOBO, E GASTEEEUGGIO, M. GAVAGNIN & G. AVIEA 2012. Ghemo-ecological studies on hexactinellid sponges from the Southern Ocean. — Naturwissenschaften , in press {Cheirimedon femoratus as test animal for toxicity.) 0KEAND, K. A. 2012. (Grustacea, Amphipoda in fresh and brackish water in Norway. Identihcation key to four Gammarus species and three ice age immigrants.) — Eauna, Oslo 64, 9-17. (In Norwegian) 0KEAND, K. A., J. 0KEAND & E 0KEAND 2012. (A surprising record of the brackish water amphipod Gammarus zMdachi in the depth of a freshwater lake.) — Eauna, Oslo 64, 18-23. (In Norwegian) OESEN, G. H., M. G. D. SMIT, J. GARROEE, I. JAEGER, T. SMITH & E. GAMUS 2011. Arctic versus temperate comparison of risk assessment metrics for 2-methyl-naphthalene. — Marine Environmental Research, 72 (4), 179-187. ( Anonyx nugax and Gammarus sp.) ORTIZ, M., G. VAREEA & R. EAEANA 2011. (A new species of amphipod in the genus Photis (Gammaridea: Photidae) from the Guban archipelago.) — Novitates Caribaea 4, 10-16. (In Spanish. Photis lecroyae n. sp. from Puerte Padre, Eas Tunas province.) OSKARSSON, H., A.-K. ERIKS SON- WIKEUND, K. EINDH & E. KUMBEAD 2011. Effect studies of human pharmaceuticals on Eucus vesiculosus and Gammarus spp. — Marine Environment Research, 74, 1-8. (Baltic Sea study) OUISSE, V, P. REIRA, A. MIGNE, G. EEROUX & D. DAVOUEI 2012. Food web analysis in intertidal Zostera marina and noltii communities in winter and summer. — Marine Biology 159, 165-175. (A study from Bretagne) 22 OZBEK, M. 2012. A new freshwater amphipod species, Gammarus katagani sp. nov., from Turkey. — Zoology of the Middle East 55, 47-54. (In Kiitahya province, W. Anatolia) OZGUL OZALP, E, M. KUTEU & A. ISCAN 2011. The effects of thallium acetate on hepatopancreatic cells of Gammarus pulex (Crustacea: Amphipoda). — Ekoloji 20 (81), 15-20. PAAVO, B. L, D. HAM, S. GOREITZ & P. K. PROBERT 2011. How does tidal submersion time affect macroinvertebrate community patterns on a temperate sheltered sandflat? — Marine & Ereshwater Research 63, 68-77. (A New Zealand study, dominant species include Torridoharpina hurleyi, Paracalliope novizealandiae', other amphipod species listed) PAGGIARDI, E., A. M. DE BIASI & E. PIAZZI 2011. Effects of Caulerpa racemosa invasion on soft-bottom assemblages in the Western Mediterranean Sea. — Biological Invasions, 13, 2677-2690. (study includes spiniventris, Phtisica marina, Metaphoxus gruneri, Perioculodes aequimanus plus hve more amphipods.) PACHECO, A. S., M. THIEE, M. E. OEIVA &J. M. RIASGOS 2011. Effects of patch size and position above the substratum during early succession of subtidal soft-bottom communities. — Helgoland Marine Research, in press DOI 10. 1007/sl01 52-01 1-0288-6. (A Chilean study, with Eudevenopus gracilipes and Heterophoxus sp among the dominant species.) PADOVANI, E. N. , M. DEEEA VINAS, E SANCHEZ & H. MIANZAN 2011. Amphipod-supported food web: Themisto gaudichaudii, a key food resource for hshes in the southern Patagonian Shelf — Journal of Sea Research 67, 85-90. PAGANEEEI, D., A. MARCHINI & A. OCGHIPINTI-AMBROGI 2011. Functional structure of marine benthic assemblages using Biological Traits Analysis (BTA): A study along the Emilia-Romagna coastline (Italy, North-West Adriatic Sea). — Estuarine, Coastal and Shelf Science 96, 245-256. (Study Ampelisca diadema) PARK, T. S., E. YE, H. J. KIE, S. G. EEE & C. H. YI 201 1. A checklist of marine invertebrates (Polychaetes, Amphipods, Decapods and Molluscs) of Goseong-gun Gangwon-do area. — Journal of Korean Nature 4, 229-253. (Not seen) PASTORINHO, M. R., T. C. TEEFER, A. M. V M. SOARES & A. J. A. NOGUEIRA 201 1. A feeding inhibition based prediction of the toxic effect of dissolved metal mixtures upon Echinogammarus marinus (Crustacea: Amphipoda) at held relevant concentrations across a latitudinal gradient. — Journal of Environmental Monitoring 13, 3343-3350. DOI: 10.1039/G1EM10499G PAVESI, E., A. DEIDUN, E. DE MATTHAEIS, R. TIEDEMANN & V KETMAIER 2012. Mitochondrial DNA and microsatellites reveal signihcant divergence in the beachhea Orchestia montagui (Talitridae: Amphipoda). — Aquatic Sciences, in press. DOI 10. 1007/s00027-012-0250-y PECK, E. S. & M. S. CEARK 2012. Understanding adaptations and responses to change in Antarctica: recent physiological and genomic advances in marine environments. — Pp 157-182 in G. di Prisco & G. Verde (Eds). Adaptation and evolution in marine environments. Volume I, From pole to pole. Springer — Verlag, Berlin-Heidelberg PEREZ-SGHUETHEISS, J. 2011. Pseudiphimediella nodosa (Dana, 1852) (Amphipoda: Gammaridea): Iphimediidae) in Eos Eagos lagoon, Chile. — Boletin de Biodiversidad de Chile 6, 41-46. PETRYASHOV, V V, M. E. DANEEIYA & A. V CHERNYSHEV 2011. Stella Vladimirovna Vassilenko (1936-2011): in memoriam. — footaxa 3098, 47-54. (With a list of her papers, and taxa described by her). PISGART, C., E MERMIEEOD-BEONDIN, C. MAAZOUZI, S. MERGOUX & P MARMONIER 2011. Potential impact of invasive amphipods on leaf litter recycling in aquatic ecosystems. — Biological Invasions, 13, 2861-2868 23 DOI 10. 1007/s 10530-01 1-9969-y (The replacement of Gammarus roeselii hy Dikerogammarus villosus in the Rlione river leads to a 66% decrease in the rate of leaf litter recycling.) PLAISANGE, L., R. BRAINARD, M. J. GALEY & N. KNOWLTON 2011. Using DNA barcoding and standardized sampling to compare geographic and habitat differentiation of crustaceans: A Hawaiian Islands example. — Diversity ^,581-591. FOR, E D 2012. Ophel, the newly discovered hypoxic chemolithotrophic groundwater biome: a window to ancient animal life. — Pp 463-478 in A. V Altenbach et al. (eds). Anoxia: Evidence for Eukaryote survival and paleontological strategies. Gellular origin, life in extreme habitats and astrobiology. Springer Science. PRIGE, A.E., M. S. MODRELE, R. L. HANNIBAL & N. H. PATEL 2010. Mesoderm and ectoderm lineages in the crustacean Parhyale hawaiensis. — Developmental Biology 34 f 256-266. RADZIEJEWSKA, T, G. FENSKE, B. WAWZRYNIAK-WYDROWSKA, P. RIEL, A. WOZNIGZKA & P. GRUSZKA 2009. The zebra mussel {Dreissena polymorpha) and the benthic community in a coastal Baltic lagoon: another example of enhancement? — Marine Ecology 30, Suppl. 1, 138-150. RAINBOW, P. S. & S. N. LUOMA 2011. Metal toxicity, uptake and bioaccumulation in aquatic invertebrates — modelling zinc in crustaceans. — Aquatic Toxicology, 105 (3-4), 455-465. [Orchestia gammarellus one of three test animals.) RAMUS, A. P. & R. B. FORWARD 2012. The physiological ecology of the supratidal amphipod Talorchestia longicornis. — Comparative Biochemistry and Physiology A, 1 61 (2), 1 59- 1 65. RASMUSSEN, J.J., R. J. MONBERG, A. BAATTRUP-PEDERSEN, N. GEDERGREEN, P. WIBERG-LARSEN, B. STROBEL & B. KRONBERG 2012. Effects of a triazole fungicide and a pyrethroid insecticide on the decomposition of leaves in the presence or absence of macroinvertebrate shredders. — Aquatic Toxicology, 118-119, 54-61. RASTRIGK, S. P. & N. M. WHITELEY 2011. Gongeneric amphipods show different abilities to maintain metabolic rates with latitude. — Physiological and Biochemical Zoology 84, 154-165. ( A study on Gammarus duebeni, G. locusta, G. oceanicus and G. setosus.) RAUQUE, G. A., R. A. PATERSON, R. POULIN & D. M. TOMPKINS 2011. Do different parasite species interact in their effects on host htness? A case study on the parasites of the amphipod Paracalliope fluviatilis. — Parasitology 138, 1176-1182. RAUQUE, G. A. & L. SEMENAS 2009. Effects of two acanthocephalan species on the reproduction of Hyalella patagonica (Amphipoda, Hyalellidae) in an Andean Patagonian lake (Argentina). — Journal of Invertebrate Pathology 100, 35-39. RAUQUE, G. A. & L. SEMENOS 2011. Parasite volume as an indicator of competition: the case of Acanthocephalus tumescens and Pseudocorynosoma sp. (Acanthocephala) in their intermediate host. — Journal of Parasitology 97, 999-1002. (The intermediate host is Hyalella patagonica.) RAUQUE, G. A. & L. SEMENOS 2012. Interactions among four parasite species in an amphipod population from Patagonia. — Journal of Helminthology, in press. DOL10.1017/S0022149X12000107. [Hyalella patagonica) REYNOLDS, L. K., L. A. GARR & K. E. BOYER 2012. A non-native amphipod consumes eelgrass inflorescences in San Francisco Bay. — Marine Ecology Progress Series 451, 107-118. (The amphipod i^Ampithoe valida.) 24 RICHARDS, V P., M. J. STANHOPE & M. S. SHPVJI 2011. Island endemism, morphological stasis, and possible cryptic speciation in two leucothoid amphipods throughout Florida and the Caribbean. — Biodiversity and Conservation, 21 (2), 343-361. (The two spp are Leucothoe ashleyae and L. kensleyi.) RIEL, M. C. van, G. van der VELDE & A. bij de VAATE 2011. Dispersal of invasive species by drifting. — Current Zoology 57, 818-827. (In the Rhine, especially Chelicorophium curvispinum Dikerogammarus villosus drift in large numbers.) RIERA, R., J. D. DELGADO, M. RODRIGUEZ, O. MONTERROSSO & E. RAMOS 2012. Macrofaunal communities of threatened subtidal maerl seabeds on Tenerife (Canary Islands, north-east Atlantic Ocean) in summer. — Acta Oceanologica Sinica 31, 98-105 (14 amphipod spp listed on p. 101) RIERA, R., J. NUNEZ & D. MARTIN 2011. Effects of thermal pollution on the soft-bottoms surrounding a power station in the Canary Islands (NE Atlantic Ocean). — Oceanology 51, 1040-1048. ( Photis longicaudata and other amphipods near the power turbines.) RIERA, R., M. RODRIGUEZ & O. MONTERROSSO 2011. Macroinfaunal assemblages in sandy seabeds of San Bias (SE Tenerife, Canary islands, NE Atlantic Ocean). — Vieraea 39, 65-76. RIERA, R., E TUYA, E. RAMOS, M. RODRIGUEZ & O. MONTERROSSO 2012. Variability of macrofaunal assemblages on the surroundings of a brine disposal. — Desalination, in press, DOI: 10. 1016/j.desal.2012.02.003 (A study from Gran Canaria. 6 amphipod spp listed in table 2). RIGOLET, C., P. EE SOUCHU, X. CAISEY & S. E DUBOIS 2011. Group sweeping: feeding activity and hltration rate in the tubicolous amphipod Haploops nirae (Kaim-Malka, 1976). — Journal of Experimental Marine Biology and Ecology 406, 29-37. ROBINSON, A., A. N. COHEN, B. LINDSEY & L. GRENIER 2011. Distribution of macroinvertebrates across a tidal gradient , Marin County, California. — San Erancisco Estuary & Watershed Science 9 (3), 1-13. (study includes Corophium alienense, Grandiderellajaponica and Traskorchestia traskiana) ROSSANO, C. & E SCAPINI 2011. Endogenous locomotor activity rhythm of two sympatric species of Talitrids (Crustacea, Amphipoda) from a sandy beach of Tuscany, Italy. — Travaux de Hnstitute Scientifique, Rabat 2011-6, 81-85. [Talitrus saltator and Orchestia gammarellus) ROY, H. E., L.-J. LAWSON HANDLEY, K. SCHONROGGE, R. L. POLAND & B. V PURSE 2011. Can the enemy release hypothesis explain the success of invasive alien predators and parasitoids? — BioControl 56, 451-468. SALA, E. & P. K. DAYTON 2011. Predicting strong community impacts using experimental estimates of per capita interaction strength: benthic herbivores and giant kelp recruitment. — Marine Ecology 32, 300-312. SCAPINI, E & L. EANINI 2011. The role of scientists in providing formal and informal information for the dehnition of guidelines, regulations or management plans for sandy beaches. — Travaux de ^Institute Scientifique, Rabat 2011-6, 87-94. SCHLACHER, T. A. & L. THOMPSON 2012. Beach recreation impacts benthic invertebrates on ocean exposed sandy shores. — Biological Conservation 747,123-132 (A study from Eastern Australia) SCHLIEF, J. & M. MUTZ 2011. Leaf decay processes during and after a supra-seasonal hydrological drought in a temperate lowland stream. — International Review of Hydrobiology 96, 633-655. SCHMIDT, C. & H. KINKLER 2011. Asseln und Flohkrebse (Isopoda, Amphipoda) des NSG Gronenborger Teiche. — Decheniana 1 64, 117-121. 25 SCHULZ, M., M. BERGMANN, K. vonJUTERZENKA & T SOETWEDEE 2010. Colonisation of hard substrata along a channel system in the deep Greenland Sea. — Polar Biology 33, 1359-1369. SEEEESEAGH, J., S. EESOURD & R. AMARA 2011. Comparison of macrobenthic assemblages of three hsh estuarine nurseries and their importance as foraging grounds. — Journal of the Marine Biological Association UK 92, 85-97. (A study from the French Channel coast. Six amphipods listed in Table 3, p. 90. Bathyporeia sarsi very numerous.) SENNA, A. R. 20 1 1 . A new species of Elasmopus (Amphipoda: Hadzioidea: Maeridae) from Suape harbor. Northeastern Brazilian coast. — Anais da Academia Brasileira de Ciencias 83, 1031-1040. [E. souzafilhoi n. sp. ) SENNA, A. R. & J. E SOUZA-FIEHO 20 1 1 . A new species of Pseudharpinia (Amphipoda: Haustorioidea: Phoxocephalidae) from Southeastern Brazilian continental shelf — Nauplius 19, 7-16. [P tupinamb a n. sp., earlier reported from the area as P dentata). SEO,J.-Y, S.-H. PARK,J.-H. FEE &J.-W. CHOI 2012. Structural changes in Macrozoobenthic Communities due to Summer Hypoxia in Gamak Bay, Korea. — Ocean Science Journal 47: 27-40 http:/ /dx.doi.org/10. 1007/ sl2601-012-0003-9 (Amphipods listed in Table 1) SHIN, S. C., J. CHO, J. K. FEE, D. H. AHN, H. FEE & H. PARK 2012. Complete mitochondrial genome of the Antarctic amphipod Gondogeneia antarctica (Crustacea, Amphipoda). — Mitochondrial DMA 23 (1), 25-27. SIGINSKI, J., K. PABIS, K. JAZDZEWSKI, A. KONOPAGKA & M. BEAZEWIGZ-PASZKOWYGZ 2012. Macrozoobenthos of two Antarctic glacial coves: a comparison with non-disturbed bottom areas. — Polar Biology 35, 355-367 (Amphipods listed in Table 2.) SIMON, R., G.JUBEAUX, A. GHAUMOT,J. EEMOINE, O. GEFEARD & A. SAEVADOR 2010. Mass spectrometry assay as an alternative to the enzyme-linked immunosorbent assay test for biomarker quantitation in ecotoxicology: Application to vitellogenin in Crustacea [Gammarus fossarurri). — Journal of Chromatography A 1217, 5109-5115. SIMPSON, R. 2011. The invasive biology of the talitrid amphipod Platorchestia platensis in North West Europe. — The Plymouth Student Scientist 4, 278-292. SIMPSON, S. E., D. WARD, D. STROM & D. E JOEEEY 2012. Oxidation of acid-volatile sulhde in surface sediments increases the release and toxicity of copper to the benthic amphipod Melita plumulosa. — Chemosphere (in press) http: / / dx.xoi.org/ 10.101 6/j.chemosphere.20 1 2.03.026 SOEER-HURTADO, M. M. &J. M. GUERRA-GARGIA 2011. Study of the crustacean community associated to the invasive Asparagopsis armata Harvey, 1855 along the coast of the Iberian peninsula. — Jooloma Baetica 22, 33-49. (Amph. on pp 40-41.) SOEYANKO, K., V SPIRIDONOV & A. NAUMOV 2011. Benthic fauna of the Gorlo Strait, White Sea: a hrst inventory based on data from three different decades from the 1920s to 2000s. — Marine Biodiversity 41, 441-453. (Amphipods listed on p. 447; Hippomedon propinquus is new for the White Sea) SOREIDE, J. E. & H. NYGARD 2012. Challenges using stable isotopes for estimating trophic levels in marine amphipods. — Polar Biology 35, 447-453. (Data on Anonyx nugax, Gammarus wilkitzkii and Themisto libellula) SOUZA-FIEHO, J. E & A. R. SENNA 2012. First record of the gonn^ Megamphopus Norman, 1869 (Crustacea, Amphipoda, Photidae) from Brazilian waters, with description of a new deep sea species. — fposytematics and Evolution 88, 71-77. [Megamphopus robustisetae n. sp. from the Campos basin, Rio de Janeiro, 1045 depth. A kew to world Megamphopus (males only) is provided). 26 STIERS, L, N. CROHAIN, G. JOSENS & E. TRIEST 201 L Impact of three aquatic invasive species on native plants and macroinvertebrates in temperate ponds. — Biological Invasions 13, 2715-2726 (A Belgian study). STUDER, A., V M. GUBIEEOS, M. D. EAMARE, R. POUEIN & D. J. BURRITT 2012. Effects of ultraviolet radiation on an intertidal trematode parasite: An assessment of damage and protection. — International Journal for Parasitology 42(5), 453-461 (Maritrema novaezealandensis in Paracalliope novizealandiae) http://dx.doi.org/ 10.1016/j.ijpara.2012.02.014 STUDER, A. & R. POUEIN 2011. Effects of salinity on an intertidal host-parasite system: Is the parasite more sensitive than its host? — Journal of Experimental Marine Biology and Ecology, in press. [Maritrema novaezealandensis in Paracalliope novizealandiae in, you guessed it. New Zealand.) STURARO, N. &J. M. GUERRA-GARGIA 2012. A new species of Caprella (Grustacea: Amphipoda) from the Mediterranean Sea. — Helgoland Marine Research 66, 33-42. [Caprella tavolarensis n. sp from Sardinia, Italy) TABAGARU, I. & D. E. DANIEEOPOE 2011. Essai d’ analyse critique des principals hypotheses concernant la phylogenie des Malacostraces (Crustacea, Malacostraca). — Travaux de Hnstitut de Speologie ‘Emile Racovitza’’ 50, 87-1 19. (Not seen, unfortunately.) TANDBERG, A.H., H. T. RAPP, G. SGHANDER, W. VADER, A. K. SWEETMAN &J. BERGE 2011. Exitomelita sigynae gen. et sp. nov: a new amphipod from the Arctic Eoke Gastle vent held with potential gill ectosymbionts. — Polar Biology, 35, 705-716. (The new genus, from 2340 m deep, 73*33. 9N, 08*09. 5E, is in the Melitidae.) doi:10.1007/s00300-0n-l 115x TATO, R., P. ESQUETE &J. MOREIRA 201 1. A new species of Ampelisca (Grustacea, Amphipoda) from NW Iberian Peninsula: Ampelisca troncosoi sp. nov. . — Helgoland Marine Research, in press DOI 10.1007/ slOl 52-01 1-0273-0 (From de Ensenada de Baiona, Galicia. A synoptic table compares the new species with 6 close relatives) TEIEI, K., P. EABADIE, G. BOURGES, A. DESPORTES & M. GHEVREUIE 2012. Bioaccumulation of polybrominated diphenyl ethers by the freshwater benthic amphipod Gammarus pulex. — Archives of Environmental Contamination and Toxicology, in press. TRIGARIGO, E., G. MAZZA, G. ORIOEI, G. ROSSANO, E SGAPINI & E GHERARDI 2010. The killer shrimp, Dikerogammarus villosus (Sowinsky 1894) , is spreading in Italy. — Aquatic Invasions 5, 211-214. TURGOTTE, C. 2011. La caprellejaponaise Caprella mutica et son impact sur Pelevage de monies Mytilus spp: Un cas de cleptoparasitisme?. — . M Sc Thesis, Universite du Quebec a Rimouski, Canada. (Not seen) d’UDEKEM d’AGOZ, G. 2012. On the genus Halirages (Grustacea, Amphipoda), with the description of two new species from Scandinavia and Arctic Europe. — European Journal of Taxonomy 7, 1-32. (Deals with Halirages cainae n. sp (69*N 12*E, 2600m) (A synoptic table shows the differences with H. caecus, H. gorbunovi and H. quadridentatus), H. quadridentatus (with H. elegans as a junior synonym), and H. stappersi n. sp. (Kara Sea) [-H. elegans s. Stappers, non Norman). A survey of and a key to all Halirages species are provided.) d’UDEKEM d’AGOZ, G. & E. A. HENDRYGKS 201 1. A new deep-sea Liljeborgia (Grustacea: Amphipoda: Eiljeborgiidae) from the DIVA II cruise in the equatorial eastern Atlantic. — Proceedings of the Biological Society of Washington 124, 198-21 1. (Deals with Liljeborgia (Lilljeborgiella) famelicosa n. sp. from the Guinea Basin, 5142m, close to L. mozambica. A key to deep water Liljeborgia is provided.) UGOEINI, A., V PASQUAEI, D. BARONI & G. UNGHERESE 2012. Behavioural responses of the supralittoral amphipod Talitrus saltator (Montagu) to trace metals contamination. — Ecotoxicology 21, 139-147. 27 UNGHERESE, G, D. BARONI, P. BRUNI, S. E. FOCARDI & A. UGOEINI 201 L Metallothionein induction in the sandhopper Talitrus saltator (Montagu) (Crustacea, Amphipoda.) — Water, Air and Soil Pollution 219, 343-351. UNGHERESE, G, A. CINGINEEEI, T. MARTEEEINI & A. UGOEINI 2012. PBDEs in the supralittoral environment: The sandhopper Talitrus saltator (Montagu) as biomonitor? — Chemosphere 86 (3), 223-227. (Quite feasible) URYUPOVA, E. E, V A. SPIRIDONOV & D. G. ZHADAN 2011. Amphipods (Crustacea; Amphipoda) associated with red algae (Rhodophyta) in Kandalaksha Bay (the White Sea, Russia). — Journal of the Marine Biological Association UK 92, 265-273. (Amphipods listed in Table 2) VAEENGIA, B. & A. GIRAEDO 2011. Structure of hyperiid amphipod assemblages on Isla Gorgona, eastern tropical Pacihc off Colombia. — Journal of the Marine Biological Association UK, 1-11. http:/ /dx.doi.org/10. 1017/ S002531541 1001780 (Amphipods listed in Table 1). VAZQUEZ-EUIS, M., P. SANGHEZ-JEREZ &J. T. BAYEE-SEMPERE. 2012. Does the invasion of Caulerpa racemosa van cylindracea affect the feeding habits of amphipods (Crustacea: Amphipoda)? — Journal of the Marine Biological Association UK, in press. http://dx.doi.org/10.1017/S002531541200Q288 . (Further studies are necessary.) VEAS, R., E. HERNANDEZ-MIRANDA, R. A. QUINONES & E D. CARRASCO 2012. Spatio-temporal biodiversity of soft-bottom macrofaunal assemblages in shallow coastal waters exposed to episodic hypoxic events. — Marine Environmental Research, in press, http://dx.doi.org/ 1 0. 1 0 1 6/j.marenvres.20 1 2.02.008 VEEEINGER, C., M. PARANT, P. ROUSEEEE, E IMMEE, P. WAGNER & P. USSEGEIO-POEATERA 2011. Comparison of arsenate and cadmium toxicity in a freshwater amphipod [Gammarus pulex). — Environmental Pollution 160, 66-73. VERGIEINO, R., K. DIONNE, C. NOZAIS, E DUFRESNE & C. BEEZIEE 2012. Genome size differences in Hyalella cryptic species. — Genome 58, 134-139. VONK, R., B. W. HOEKSEMA & D. JAUME 201 1. A new interstitial Psammogammarus (Crustacea, Amphipoda, Melitidae) from Gura Ici Island, off western Halmahera (North Moluccas, Indonesia), and an overview of the genus. — fpoKeys 128, 53-73. [Psammogammarus wallacei n. sp. The ‘overview covers the entire Eriopisa group of the Melitidae, and the synoptic Table 1 compares all Psammogammarus species. The taxa Eriopisa inaequicaudata and E. mochinno are removed from Eriopisa, and probably do not even belong to the Eriopisa group of genera.) WAGEEE, H., A. KEUSSMANN-KOEB, M. KUHEMANN, G. HASZPRUNAR, D. EINDBERG, M A. KOCH & J. W. WAGEEE 2011. The taxonomist — an endangered race. A practical proposal for its survival. — Erontiers in Zoology 8-25, 1 pp. WAE, D. V. d. & P. M. J. HERMAN 2011. Ecosystem engineering effects of Aster tripolium and Salicornia procumbens salt marsh on macrofaunal community structure. — Estuaries and Coasts 35 (3), 714-726. WATKINS, J. M., E. G. RUDSEAM, E. E. MIEES & M. A. TEECE 2012. Coexistence of the native benthic amphipod Diporeia spp. and exotic dreissenid mussels in the New York Finger Fakes. — Journal of Great Lakes Research 38(2), 226-235. http://dx.doi.Org/10.1016/j.jglr.2012.02.001 . WEERMAN, E. J., P. M. J. HERMAN &J. v. d. KOPPEE 2011. Macrobenthos abundance and distribution on a spatially patterned intertidal flat. — Marine Ecology Progress Series 440, 95-103. (Studies on Hydrobia ulvae and Corophium volutator.) WESSEES, H., U. KARSTEN, G. WIENGKE & W. HAGEN 2012. Fatty acids as potential trophic markers in Arctic benthic systems: feeding experiments with nine diets of macroalgae. Polar Biology 35: 555-565. Doi: 10.1007/ s00300-0 11-1101-3 [Gammarellus homari is amphipod used) 28 WESTRAM, A. M. J. JOKELA, C. BAUMGARTNER & L KEEEER 201 L Spatial distribution of cryptic species diversity in European freshwater amphipods [Gammarus fossarum) as revealed by pyrosequencing. — PLOS One 6-8, 6 pp (On the distribution of three cryptic taxa in Central Europe) WHITE, K. N. 201 1. Caribbean Eeucothoidae (Crustacea: Amphipoda) of Panama. — Gulf and Caribbean Research 23, 23-35. (Deals With Anamixis cavatura, A. vanga, Leucothoe ashleyi, L. barana, L. flammosa, L. laurensi, L ubouhu, L. wuriti and L. sp. C Thomas & Klebba, 2007. A key to Caribbean Eeucothoidae in Panama is provided.) WHITE, K. N. 201 1. Nuclear 18S rDNA as a species-level molecular marker for Eeucothoidae. — Journal of Crustacean Biology 31, 710-716. WHITE, K. N. 201 1. A taxonomic review of the Eeucothoidae (Crustacea: Amphipoda). — Jpotaxa 3078, 1-1 13. (This PhD monograph contains a survey of all species, with diagnoses and identihcation keys.) WHITE, K. N. &J. D. REIMER 2012. Commensal Eeucothoidae (Crustacea, Amphipoda) of the Ryukyu Archipelago, Japan. Part I: ascidian-dwellers. — JpoKeys 163, 13-35. (Deals with Leucothoe amamiensis n. sp., L. elegans n. sp., L. nathani n. sp., L. obuchii n. sp., L trulla n. sp., L vulgaris n. sp., and Paranamixis thomasi n. sp., all from the Ryukyu Islands. A key to ascidian-dwelling species from the area is provided.) WHITE, K. N. &J. D. REIMER 2012. Commensal Eeucothoidae (Crustacea, Amphipoda) Of the Ryukyu Archipelago, Japan. Part II. Sponge-dwellers. — JooKeys 166, 1-58. (Deals with Leucothoe akaoni n. sp., L. bise n. sp., L daisukei n. sp., L. hashi n. sp., L lecroyae n. sp., L nagatekubi n. sp., L nurunuru n. sp., L ouraensis n. sp., L togatta n. sp., L toribe n. sp., and L. zanpa n. sp., all from the Ryukyu Islands. A key to sponge-dwelling species from the area is provided.) WHITE, K. N. &J. D. REIMER 2012. Commensal Eeucothoidae (Crustacea, Amphipoda) of the Ryukyu Archipelago, Japan. Part III: coral rubble dwellers. — ZooKeys 173, 1 1-50. (Deals WithAnamixis sentan n. sp. (Okinawa), Leucothoe akaisen n. sp. (Okinawa), L. akuma n.sp. (Okinawa), L chiisainame n. sp. (Kagoshima), L. enko n. sp. (Kagoshima), L kebukai n. sp. (Okinawa), and Paranamixis misakiensis. An identihcation key to all Ryukyu Eeucothoidae is provided) WHITEOW, W. E. &J. N. GRABOWSKI 2011. Examining how landscapes inhuence benthic community assemblages in seagrass and mudhats habitats in southern Maine. — Journal of Experimental Marine Biology and Ecology 411, 1-6. WIJNHOVEN, S., G. v. d. VEEDE & H. HUMMEE 2011. Corophium multisetosum Stock, 1952 an exotic invasive species in Europe? Distribution, habitat, and recent observations in the Netherlands. — Crustaceana 84, 975-1011. (Not seen) WIEHEEM, E M. & D. NEESON 2012. A non-lethal approach to estimate whole-body ^^G and ^^N stable isotope ratios of freshwater amphipods using walking legs. — Invertebrate Biology (in press) DOI: 10. 1 1 1 1 /j. 1744-7410.2012.00259.X WINFIEED, L, S. GHAZARO-OEVERA, M. ORTIZ & U. PAEOMO-AGUAYO 2011. (Updated checklist of marine invasive species of amphipods (Peracarida:Gammaridea and Corophiidea) from Mexico.) — Revista de Biologia Marina y Oceanografia 46, 349-361. (In Spanish, with data on 1 1 species considered to be invasive. Most are North American.) YU, O. H. & H.-E. SUH 2011. Secondary production of the eusirid amphipod Pontogeneia rostrata Gurjanova, 1938 (Crustacea: Peracarida) on a sandy shore in Korea. — Ocean Sciences Journal 46, 21 1-217. ZAMANPOORE, M., M. GRABOWSKI, M. POGKE & E SGHIEMER 2011. Taxonomic review of freshwater Gammarus (Crustacea: Amphipoda) from Iran. — Jpotaxa 3140, 1-14. (Deals with Gammarus anodon, G. bakhteyaricus, G. 29 baloutchi, G. crinicaudatus, G. hegmatanensis, G. komareki, G. lacustris, G. lobifer, G. loejfleri, G. lordeganensis, G. paricrenatus, G. parthicus, G. pretzmanni (with G. projectus as synonym), G. pseudosyriacus (with G. miae and G. plumipes as synonyms. This species has also often been misidentihed in the literature), G. sepidannus, G. shirazinus, G. sirvannus, and G. zagrosensis. A key to all Gammarus in Iran is provided.) ZHANG, Z.-Q^ 2011. Animal biodiversity: An introduction to higher-level classihcation and taxonomic richness. — Zootaxa3148, 7-12. ZHANG, Z.-Q 2011. Phylum Arthropoda von Siebold, 1848. In: Zhang, Z.-Q (Ed.) Animal biodiversity: An introduction to higher-level classihcation and taxonomic richness. — 3148, 99-103. ZUBROD, J. B. & M. BUNDSGHUH 2011. Ecotoxicological impact of the fungicide tebuconazole on an aquatic decomposer-detritivore system. Environmental Chemistry 30(12), 2718-2724. New amphipod taxa in AN 36 1. Families and subfamilies Austroniphargidae lannilli, Krapp & Ruffo, 2011 Conicostomatinae Eowry & Stoddart, 2012 Pachynidae Eowry & Stoddart, 2012 2. Genera and subgenera Amphorites Eowry & Stoddart, 20 1 2 Cephaloecetes Just, 2012 Davidia lannilli, Krapp & Ruffo, 2011 Exitomelita Tandberg et ah, 2011 Kairos Krapp -Schickel & Muller, 20 1 1 Libertinia lannilli, Krapp & Ruffo, 201 1 Klebang Azman & Othman, 2012 Maarrka Finston et ah, 2011 Mucrocalliope Ariyama & Azuma, 2011 Neoecetes Just, 2012 Reinhardia lannilli, Krapp & Ruffo, 2011 Renella Eowry & Stoddart, 2012 Smaraldia Eowry & Stoddart, 2012 Ultimachelium Eowry & Stoddart, 2012 Eysianassidae Conicostomatinae Ischyroceridae Austroniphargidae Melitidae Garangoliopsidae Austroniphargidae Unciolidae Paramelitidae Paracalliopiidae Ischyroceridae Austroniphargidae Pachynidae Pachynidae Pachynidae 3. Species and subspecies akaisen White & Reimer, 2012 [Leucothoe) akaoni White & Reimer, 2012 {Leucothoe) akuma White & Reimer, 2012 [Leucothoe) albomaculosus Just, 2012 [Rhinoecetes) amamiensis White & Reimer, 2012 [Leucothoe) andreae Coleman & Maturana Heinz, 2011 [Curidia) angelikae Eorz, Smith, Einse & Steinke, 2011 [Epimeria) angulosa Eowry & Stoddart, 2012 [Ligorella) annasona Eowry & Stoddart, 2012 [Amphorites) ashleyi Eorz, 2012 [Epimeria) aurifex lannilli, Krapp & Ruffo, 2011 [Dussartiella) barnardi Azman & Othman, 2012 [Klebang bise White & Reimer, 2012 [Leucothoe) Eeucothoidae Eeucothoidae Eeucothoidae Ischyroceridae Eeucothoidae Ochlesidae Epimeriidae Pachynidae Conicostomatinae Epimeriidae incertae sedis Unciolidae Eeucothoidae 30 brevirostris Just, 2012 [Rhinoecetes) cainae d’Udekem d’Acoz, 2012 {Halirages) cedrici Krapp-Schickel, 201 1 [Prometopd] chiisainame White & Reimer, 2012 [Leucothoe) claudei Krapp-Schickel, 2011 (Antatelson) clydensis King & Leys, 2011 {Austrochiltonia) coclearisjust, 2012 {Rhinoecetes) conipesjust, 2012 {JVeoecetes) cooperi King & Leys, 2011 {Austrochiltonia) daisukei White & Reimer, 20 1 2 {Leucothoe) darwinense Lowry & Stoddart, 2012 {Scopolostoma) dimorpha lannilli, Krapp & Rruffo, 2011 {Reinhardia) dinoceros Just, 2012 {Rhinoecetes) elegans White & Reimer, 2012 {Leucothoe) eltanin Lowry & Stoddart, 2012 {Ekelofia) enigmaticusjust, 2012 {Cephaloecetes) enko White & Reimer, 2012 {Leucothoe) epa Lowry & Stoddart, 2012 {Prachynella) etheli Finston et ah, 201 1 {Maarrka) famelicosa d’Udekem d’Acoz & Hendrycks, 2011 {Liljeborgia) formosa Lowry & Stoddart, 2012 {Figorella) franklin Lowry & Stoddart, 2012 {Figorella) freemanae Kilgallen, 201 1 {Apohyale) fucaense Lowry & Stoddart, 2012 {Pachychelium) hangangense Kim, 2012 {Sinocorophium) hashi White & Reimer, 2012 {Leucothoe) henriki Koppen & Coleman, 2011 {Seba) inornatus Myers, Rigolet, Thiebaut & Dubois, 20 1 2 {Photis) jejuensis Kim, Hendrycks & Lee, 2011 {Guernea) katagani Ozbek, 2012 [Gammarus] kebukai White & Reimer, 20 1 2 {Leucothoe) keurboomstrandense Lowry & Stoddart, 2012 {Scopolostoma) latibasis lannilli, Krapp & Ruffo, 2011 {Libertinid) lecroyae White & Reimer, 2012 {Leucothoe) lecroyae Ortiz, Varela & Lalana, 2011 {Photis) longitelson lannilli, Krapp & Ruffo, 2011 {Libertinia) luce Lowry & Stoddart, 20 1 2 {Drummondia) marlo Lowry & Stoddart, 2012 {Drummondia) melakaensis Azman & Othman, 2012 {Grandidierella) meridianus Just, 2012 {Rhinoecetes) nagatekubi White & Reimer, 2012 {Leucothoe) namhaensis Kim, Hendrycks & Lee, 2011 {Guernea) nathani White & Reimer, 2012 {Leucothoe) nor ah Lowry & Stoddart, 2012 {Scopolostoma) novazealandica Lorz, Linse, Smith & Steinke, 20 1 2 {Rhachotropis) nurumuru White & Reimer, 2012 {Leucothoe) obsolescens Lowry & Stoddart, 2012 {Pachynus) obuchii White & Reimer, 2012 {Leucothoe) oculata Lowry & Stoddart, 2012 {Prachynella) ouraensis White & Reimer, 2012 {Leucothoe) paguri Marin & Sinelnikov, 2012 {Metopelloides) papanuiensis Kilgallen, 201 1 {Apohyale) polynesus Krapp-Schickel & Muller, 2011 {Flasmopus) rhinoceros Just, 2012 {Rhinoecetes) Ischyroceridae Calliopiidae Stenothoidae Leucothoidae Stenothoidae Ghiltoniidae Ischyroceridae Ischyroceridae Ghiltoniidae Leucothoidae Gonicostomatinae Austroniphargidae Ischyroceridae Leucothoidae Pachynidae Ischyroceridae Leucothoidae Pachynidae Paramelitidae Liljeborgiidae Pachynidae Pachynidae Hyalidae Pachynidae Gorophiidae Leucothoidae Sebidae Photidae Dexaminidae Gammaridae Leucothoidae Gonicostomatinae Austroniphargiidae Leucothoidae Photidae Austroniphargidae Pachynidae Pachynidae Aoridae Ischyroceridae Leucothoidae Dexaminidae Leucothoidae Gonicostomatinae Eusiridae Leucothoidae Pachynidae Leucothoidae Pachynidae Leucothoidae Stenothoidae Hyalidae Maeridae Ischyroceridae 31 robustisetae Souza-Filho & Senna, 2012 [Megamphopus) segregans Krapp-Schickel & Muller, 201 1 [Kairos) sentan White & Reimer, 2012 {Anamixis) shijiki Lowry & Stoddart, 2012 [Prachynella) shimantoensis Ariyama & Azuma, 2011 [Mucrocalliope) sigynae Tandberg et ah, 201 1 (Exitomelita) souzafilhoi Senna, 201 1 [Elasmopus) spelaea Bueno & Cardoso, 201 1, in Cardoso et al.) [Hyalelld] spinicaudata lannilli, Krapp & Ruffo, 2011 [Davidid] spinidactylus lannilli, Krapp & Ruffo, 20 1 1 {Sandro) springthorpei Lowry & Stoddart, 20 1 2 {Smaraldia) stappersi d’Udekem d’Aeoz, 2012 [Halirages) tac Lowry & Stoddart, 2012 {Ultimachelium) tavolarensis Sturaro & Guerra-Gareia, 20 1 2 {Caprella) togatta White & Reimer, 2012 {Leucothoe) toribe White & Reimer, 20 1 2 [Leucothoe) tridentata Lowry & Stoddart, 212 [Drummondid] troncosoi Tato, Esquete & Moreira, 2011 {Ampeliscd) tropicale Lowry & Stoddart, 20 1 2 [Pachychelium) trulla White & Reimer, 2012 [Leucothoe) tupinamba Senna & Souza-Filho, 2011 [Pseudharpinia) vulgaris White & Reimer, 2012 [Leucothoe) wallacei Vonk, Hoeksema &Jaume, 2011 [Psammogammarus) weeliwolli Finston et ah, 2011 [Maarrka) yatala Lowry & Stoddart, 2012 [Ocosingo) zanpa White & Reimer, 2012 [Leucothoe) Photidae Garangoliopsidae Leueothoidae Paehynidae Paraealliopiidae Melitidae Maeridae Dogielinotidae Austroniphargidae Austroniphargidae Paehynidae Galliopiidae Paehynidae Caprellidae Leueothoidae Leueothoidae Paehynidae Ampeliseidae Paehynidae Leueothoidae Phoxoeephalidae Leueothoidae Melitidae Paramelitidae Conieostomatinae Leueothoidae 4. New taxa ranked taxonomically after families Ampeliseidae Aoridae Austroniphargidae Galliopiidae Caprellidae Garangoliopsidae Ghiltoniidae C onicostomatinae Gorophiidae Dexaminidae Dogielinotidae Epimeriidae Eusiridae Gammaridae Hyalidae Isehyroeeridae Ampelisea troncosoi Grandidierella melakaensis Davidia spinicaudata Libertinia latibasis, longitelson Reinhardia dimorpha Sandro spinidactylus Halirages cainae, stappersi Caprella tavolarensis Kairos segregans Austroehiltonia clydensis, cooperi Amphorites annasona Oeosingo yatala Seopolostoma darwinense, keurboomstrandense, norah Sinoeorophium hangangense Guernea jejuensis, namhaensis Hyalella spelaea Epimeria angelikae, ashleyi Rhachotropis novazealandica Gammarus katagani Apohyale freemanae, papanuiensis Cephaloecetes enigmaticus Neoecetes conipes Rhinoeeetes albomaculosus, brevirostris, coclearis, dinoceros, meridianus, rhinoceros 32 Lm&mmsp newsletter Liljeborgiidae Maeridae Meliddae Ochlesidae Pachynidae Paracalliopiidae Paramelitidae Photidae Phoxocephalidae Sebidae Stenothoidae Unciolidae Incertae sedis ^ ® Anamixis sentan Leucothoe akaisen, akaoni, akuma, amamiensis, bise, chiisainame, daisukei, elegans, enko, hashi, kebukai, lecroyae, nagatekubi, nathani, nurunuru. obuchii, ouraensis, togatta, toribe, trulla, vulgaris, zanpa Paranamixis thomasi Liljeborgia famelicosa Elasmopus polynesus, souzafilhoi Exitomelita sigynae Psammogammams wallacei Guridia andreae Drummondia luce, marlo, tridentate Ekelofia eltanin Figorella angulosa, formosa, franklin Pachychelium fucaense, tropicale Pachynus obsolescens Prachynella epa, oculata, shijiki Renella Smaraldia springthorpei Mucrocalliope shimantoensis Maarrka etheli, weeliwolli Megamphopus robustisetae Photis inornatus, lecroyae Pseudharpinia tupinamba Seba henriki Antatelson claudei Metopelloides paguri Prometopa cedrici lOebang barnardi Dussartiella aurifex 33 Amphipod newsletter 36 NEW AMPHIPOD GENERA (AN 10 - 35) AGANTHOGAMMARIDAE Sg Ancyracanthus Kamaltynov, 2001 Gammarus godlewskii victorii AN24-14 Aspretus Kamaltynov, 2001 Asprogammarus puer AN24-15 Asprogammarus Bazikalova, 1975 Gammarus rhodophthalmus AN 14-38 Sg Caecogammarus Kamaltynov, 2001 Plesiogammarus gerstaeckeri brevis AN24-15 Cornugammarus Kamaltynov, 2001 Polyacanthus maximus AN24-14 Dedyuola Kamaltynov, 2001 Gammarus armatus AN24-14 Diplacanthus Kamaltynov, 2001 Acanthogammarus godlewskii brevispinus AN 24-14 Dorogostaiskia Kamaltynov, 2001 Spinacanthus insularis AN24-14 Eremogammarus Kamaltynov, 2001 Gammarus puella AN24-15 Inobsequentus Takhteev, 2000 Poekilogammarus galini AN22-64 Koshovia Bazikalova, 1975 K. mirabilis AN 9-43 Nyctoporea Kamaltynov, 2001 Poekilogammarus sukaczewi AN24-15 Oxyacanthus Kamaltynov, 2001 Polyacanthus flavus AN24-14 Palicarinus Barnard & Barnard, 1983 Gammarus puzylli AN15-14 Sentogammarus Kamaltynov, 2001 Gammarus zienkowiczii AN24-15 Smaragdogammarus Bazikalova, 1975 Gammarus smaragdinus AN 14-38 Supernogammarus Kamaltynov, 2001 Sg Variogammarus Takhteew, 1 995 Plesiogammarus longicornis AN24-15 AGANTHONOTOZOMATIDAE Acanthonotozomopsis Wading & Holman, 1980 Acanthonotozomella pushkini Nodotergum Bellan-Santini, 1972 N. bicarinatum AN 2-18 Ochlesodius Eedoyer, 1982 O. spinicornis AN15-34 Stegopanoploea Karaman, 1980 Panoploea joubini AN15-31 AGANTHONOTOZOMEEEIDAE Amatiguakus Goleman & Barnard, 1991 A. forsberghii AN19-11 Paracanthonotozoma Bellan-Santini, 1971 P. trispinosum AN 2-18 AETIOPEDESIDAE Aetiopedes Moore & Myers, 1 988 A. gracilis AN 17-4 AEIGEEEIDAE Apotectonia Barnard & Ingram, 1990 A. heterostegos AN 19-8 Diatectonia Barnard & Ingram, 1990 D. typhodes AN 19-8 Tectovalopsis Barnard & Ingram, 1990. T. wegeneri AN 19-8 Transtectonia Barnard & Ingram, 1 990 T. torrentis AN 19-8 AMARYEEIDAE Bamarooka Eowry & Stoddart, 2002 Amaryllis bathycephala AN24-17 Devo Eowry & Stoddart, 2002 D. grahami AN24-17 Erikus Eowry & Stoddart, 1987 E. dahli AN17-14 34 Paravijaya Ren, 1998 P apiculata AN22-54 Pseudamaryllis Andres, 1 98 1 P nonconstricta AN15-11 Wonga Lowry & Stoddart, 2002 W. wonga AN24-17 AMATHILLOPSIDAE Jeanjustia Lowry & Myers, 2003 J. per da AN26-23 AMPHILOGHIDAE Afrogitanopsis Karaman, 1980 Gitanopsis paguri AN16-19 Apolochus Hoover & Bousfield, 2001 Amphilochus neapolitanus AN23-22 Gitanopsilis Rauschert, 1 994 G. amissio AN27-37 Hourstonius Hoover & Bousfield, 2001 Gitanopsis vilordes AN23-22 Paramphilochoides Lincoln, 1979 Amphilochoides intermedins AN13 Paramphilochus Ishimaru & Ikehara, 1986 P parachelatus AN 17-40 Pseudopeltocoxa Schiecke, 1977 P gibbosa AN 10-48 Rostrogitanopsis Karaman, 1980 Gitanopsis mariae AN16-19 AMPITHOIDAE Amphyllodomus Just, 1977 A. incurvaria AN 10-34 Sg Melanesius Ledoyer, 1984 Examphithoe cooki AN 16-2 2 Peramphithoe Gonlan & Bousfield, 1982 Ampithoe femorata AN 15-20 Plumithoe Barnard & Karaman, 1991 Ampithoe plumicornis AN 19-4 Pseudoamphithoides Ortiz, 1976 P bacescui AN 10-5 2 Pseudopleonexes Gonlan, 1982 Pleonexes lessoniae AN 15-20 ANISOGAMMARIDAE Annanogammarus Bousfield, 1979 Gammarus annadalei AN12-19 Barrowgammarus Bousfield, 1979 Anisogammarus macginitiei AN12-19 Carineogammarus Bousfield, 1979 Eogammarus makarovi AN 12-20 Eurypodogammarus Hon, Morino & Li L, 2005 E. helobius AN31-12 ?Fuxiana Sket, 2000 E yangi AN22-59 Fuxigammarus Sket & Liser, 2009 E antespinosus AN34-51 Jesogammarus Bousfield, 1979 Anisogammarus jesoensis AN12-19 Locus togammarus Bousfield, 1979 Gammarus locustoides AN12-19 Ramellogammarus Bousfield, 1979 Gammarus ramellus AN12-19 Spasskogammarus Bousfield, 1979 S. spasski AN12-19 Sg Spinulogammarus Tzvetkova, 1972 Gammarus ochotensis AN 2-23 AORIDAE Aorella Myers, 1981 A. multiplex AN 16-2 7 Archaeobemlos Myers, 1988 Autonoe philacantha AN 17-4 Arctolembos Myers, 1979 Microdeutopus arcticus AN13 Australomicrodeutopus Myers, 1988 Microdeutopus haswelli AN17-15 Sg Bigrandidierella Karaman, 1986 Microdeutopus megnae AN 17-42 Columbaora Gonlan & Bousfield, 1982 G. cyclocoxa AN 15-20 Sg Globosolembos Myers, 1985 Autonoe smith! AN 17-46 Meridiolembos Myers, 1 988 Lembos hippocrenes AN17-15 Paragrandidierella Ariyama, 2002 P minima AN24-3 Paramicrodeutopus Myers, 1988 Microdeutopus schmitti AN17-15 Plesiolemb os Myers, 1988 Lembos rectangulatus AN17-15 Protolembos Myers, 1 988 Lembos chiltoni AN17-15 Pseudobemlos Ariyama, 2004 P serratus AN27-2 Tetbybemlos Ariyama, 2004 T japonicus AN27-2 Tetbylembos Myers, 1988 Lembos viguieri AN17-15 35 ARISTIIDAE Boca Lowry & Stoddart, 1997 B. campi AN22-37 Memana Stoddart & Lowry, 2010 M. sarda AN34-53 Pratinas Stoddart & Lowry, 2009 P ludmilla AN34-53 ARTLSIIDAL Artesia Holsinger, 1980 A. subterranea AN13 AUSTRONIPHARGIDAL Dussartiella Ruffo, 1979 D. madegassa AN13 Sandro Karaman & Barnard, 1979 Austroniphargus starmuhlneri AN 12-2 7 BOGIDILLLIDAL Actogidiella Stock, 1981 A. cultrifera AN 15-49 Afridiella Karaman & Barnard, 1979 Bogidiella somala AN12-17 Sg Antillogidiella Stock, 1981 Bogidiella martini AN 15-49 Arganogidiella Koenemann & Holsingei ’, 1999 Bogidiella arganoi AN22-32 Argentinogidiella Koenemann & Holsinger, 1 999 Bogidiella hormocollensis AN22-32 Aurobogidiella Karaman, 1988 Bogidiella italica AN17-25 Bermudagidiella Koenemann & Holsinger, 1 999 Bogidiella antillensis AN22-32 Bogidomma Bradbury & Williams, 1995 B. australis AN21-11 Cabogidiella Stock & Vonk, 1992 G. littoralis AN20-35 Sg Dyticogidiella Grosso & Glaps, 1985 Bogidiella talampuyensis AN 17-39 Sg Eobogidiella Karaman, 1981 Bogidiella purmarmacensis AN 15-31 Fidelidiella Jaume, Gracia & Boxshall, 2007 L pectinata AN33-12 Grossogidiella Koenemann & Holsinger, 1999 Patagongidiella mauryi AN22-32 Sg Guagidiella Stock, 1 98 1 Bogidiella holsinger! AN 15-49 Sg Hagidiella Stock, 1985 Bogidiella prionura AN 16-34 Hebraegidiella Karaman, 1 988 H. bromleyana AN17-25 Indogidiella Koenemann & Holsinger, 1 999 Bogidiella sarawacensis AN22-32 Maghrebidiella Diviacco & Ruffo, 1985 M. maroccana AN 17-37 Marigidiella Stock, 1981 Bogidiella brasiliensis AN 15-49 Sg Marinobogidiella Karaman, 1981 Bogidiella tyrrhenica AN 15-31 Sg Medigidiella Stock, 1981 Bogidiella chappuisi AN 15-49 Megagidiella Koenemann & Holsinger, 1 999 M. ezul AN22-31 Sg Mesochtongidiella Grosso & Fernandez, 1985 Bogidiella tucumanensis AN19-15 Sg Mexigidiella Stock, 1981 Bogidiella tabascensis AN 15-49 Nubigidiella Karaman, 1988 Bogidiella nubica AN17-25 Omangidiella lannilli, Holsinger, Ruffo & Vonk, 2006 O. parvidactyla AN31-13 Sg Orchestigidiella Stock, 1 98 1 Bogidiella orchestipes AN 15-49 Parabogidiella Holsinger, 1 980 P americana AN13 Patagongidiella Grosso & Fernandez, 1993 P. mauryi AN21-22 Racovella Jaume, Gracia & Boxshall, 2007 R. birramea AN33-12 Somagidiella Stock, 1981 Bogidiella somala AN 15-49 Spelaeogammarus da Silva Brum, 1975 S. bahiensis AN 7-33 Stockigidiella lannilli, Holsinger, Ruffo & Vonk, 2006 36 S. aequimana AN31-13 Sg Stygogidiella Stock, 1 98 1 Bogidiella bredini AN 15-49 Sg Xystriogidiella Stock, 1984 Bogidiella capricornia AN 16-34 BOLTTSIIDAE Bolttsia Griffiths, 1976 B. minuta AN 8-29 GALLIOPIIDAE Callaska Barnard, 1978 Galliopiella pratti AN 10-3 7 Calliopiurus Bushueva, 1986 G. excellens AN17-35 Domicola Pretus & Albello, 1993 D. lithodesi AN20-29 Lopyastis Thurston, 1974 Atylopsis signiensis Membrilopus Barnard & Karaman, 1987 Metaleptamphopus membrisetata AN 17-6 Paracalliopiella Tzvetkova & Kudrjaschov, 1975 Eeptamphopus litoralis AN 9-55 Spongula Schiecke, 1973 S. depressa AN 4-28 Tylosapis Thurston, 1974 Atylopsis dentata GAPREEEIDAE Caprellaporema Guerra-Garcia, 2003 G. subantarctica AN26-13 Chaka Griffiths, 1974 G. leoni AN 4-23 Cubodeutella Ortiz, Guerra-Garcia & Ealana, 2009 G. cavernicola AN34-43 Heterocaprella Arimoto, 1976 H. clavifera AN 8-18 Jigurru Guerra-Garcia, 2006 J. vailhoggett AN31-10 Liriopes Arimoto, 1978 E. lunaticus AN12-17 Mayericaprella Guerra-Garcia, 2006 M. arimotoi AN31-10 Paradicaprella Hirayama, 1 990 P brucei AN19-16 Pedotrina Arimoto, 1978 P globosa AN12-17 Pedunculocaprella Kaim-Malka, 1983 P antennata AN16-19 Premohemiaegina Arimoto, 1978 P sola AN12-16 Pretritella Arimoto, 1 980 P divina AN13 Proto aeginella Eaubitz & Mills, 1972 P muriculata AN 2-28 Prototritella Arimoto, 1976 P ishigakensis AN12-16 Pseudoprellicana Guerra-Garcia, 2006 P johnsoni AN31-10 Quadrisegmentum Hirayama, 1 988 Q triangulum AN 17-3 Tanzacaprella Guerra-Garcia, 2001 T tanzaniensis AN24-10 Tropicaprella Guerra-Garcia & Takeuch; i, 2003 T minuta AN25-10 GEINIDAE Taihape Barnard, 1972 T karori AN 3-39 Waitomo Barnard, 1972 W. manene AN 3-39 GHEIDAE Cheus Thurston, 1982 G. annae AN 15-5 2 GHEIROGRATIDAE Aurohornellia Barnard & Karaman, 1982 Tulearogammarus sinuatus AN15-14 Cheirocarpochela Ren & Andres, 2006 G. sinica AN31-25 Cottarellia Ruffo, 1994 G. minima AN21-47 Degocheirocratus Karaman, 1985 D. spani AN17-12 Incratella Barnard & Drummond, 1982 Gheirocratus inermis AN15-13 37 Sg Indocratus Eedoyer, 1982 Gheirocratus inermis AN15-34/5 Prosocratus Barnard & Drummond, 1982 P. butcheri AN15-13 GHIETONIINAE Arabunnachiltonia King, 2009 A. murphyi AN34-30 Phreatochiltonia Zeidler, 1991 P anophthalma AN20-40 Wangiannachiltonia King, 2009 W. guzikae AN34-30 GONDUKIIDAE Condukius Barnard & Drummond, 1982 G. karkan AN15-13 Otagia Barnard & Karaman, 1 99 1 Platyischnopus neozelanicus AN 19-4 GOROPHIINAE Americorophium Bousfield & Hoover, 1997 Gorophium spinicorne Anonychocheirus Moore & Myers, 1983 A. riehardsoni Apocorophium Bousfield & Hoover, 1997 Gorophium aeutum Chaetocorophium Karaman, 1979 Paracorophium lueasi Chelicocorophium Bousfield & Hoover, 1997 Gorophium eurvispinum Crassicorophium Bousfield & Hoover, 1997 Gorophium erassieorne Eocorophium Bousfield & Hoover, 1997 Gorophium kitamari Hirayamaia Bousfield & Hoover, 1997 Gorophium mortoni Laticorophium Bousfield & Hoover, 1997 Gorophium baeoni Lobatocorophium Bousfield & Hoover, 1997 Gorophium lobatum Medicocorophium Bousfield & Hoover, 1997 Gorophium aeuleatum Microcorophium Bousfield & Hoover, 1997 Gorophium sextonae miospinulosum Monocorophium Bousfield & Hoover, 1997 Gorophium insidiosum Sinocorophium Bousfield & Hoover, 1997 Gorophium sinense Stenocorophium Karaman, 1979 S. bowmani GRANGONYGTIDAE Amurocrangonyx Sidorov & Holsinger, 2007 Grangonyx arsenjevi AN32-24 Prefalklandella Stoek & Platvoet, 1991 Falklandella euspidata AN20-34/5 Stygonyx Bousfield & Holsinger, 1 989 S. courtneyi AN 17-22 Uronyctus Stoek & Ilifie, 1990 U. longieaudus AN 19-2 7 GRYMOSTYGIDAE Crymostygius Kristjansson & Svavarsson, 2004 G. thingvallensis AN26-20 GYAMIDAE Sg Apocyamus Margolis, MeDonald & Bousfield, 2000 Gyamus seammoni AN22-40 Sg Mesocyamus Margolis, MeDonald & Bousfield, 2000 Gyamus mesorubraedon AN22-40 Sg Orcinocyamus Margolis, McDonald & Bousfield, 2000 Gyamus orcini AN22-40 Scutocyamus Eincoln & Hurley, 1974 S. parvus AN 5-29 GYPROIDEIDAE Gbroidea Eowry & Azman, 2008 G. dingaalana AN33-16 AN21-10 AN 15-39 AN21-10 AN13 AN21-10 AN21-10 AN21-10 AN21-10 AN21-11 AN21-10 AN21-10 AN21-10 AN21-10 AN21-10 AN 12 -26 38 Moolapheonoides Barnard, 1974 M. kadee AN 4-30 Terepeltopes Hirayama, 1983 T dolichorhunia AN 15-2 7 Unguj a Griffiths, 1976 U. yaya AN 8-29 Victorhensenioides Rauschert, 1996 V arntzi AN21-45 DEXAMINIDAE Dexaminoculus Eowry, 1981 Sphaerophthalmus grobbeni AN 15-36 Sebadexius Eedoyer, 1984 S. neocaledoniensis AN 16-2 2 DIDYMOGHEEIIDAE Apodidymochelia Thurston, 1997 A. castellata AN21-57 DIKWIDAE Dikwa Griffiths, 1974 D. acrania AN 5-27 DOGIEEINOTODAE Sg Austrohyalella Bousheld, 1996 Hyalella neonoma AN21-7 Dogielinoides Bousheld, 1982 Dogielinotus golikovi AN15-17 Eohaustorioides Bousheld & Tzvetkova, 1982 Haustorioides japonicus AN15-17 Exhyalella Stebbing, 1917 E. natalensis AN23-32 Marinohyalella Eazo-Wasem & Gable, 2001 Hyalella richardi AN23-32 Sg Mesohyalella Bousheld, 1996 Hyalella curvispina AN21-7 Parhaustorioides Ren, 2006 P littoralis AN31-25 Proboscinotus Bousheld, 1982 Dogielinotus loquax AN15-17 DUEIGHIIDAE Dulichiopsis Eaubitz, 1977 Dulichia spinossisima AN9-57 Paradyopedos Andres & Rauschert, 1 990 P. antarcticus AN 19-7 Pseudodulichia Rauschert, 1 990 Dulichia antarctica AN 19-24 EPIMERIIDAE Spindlerella Brandt & Vassilenko, 1 995 S. groenlandica AN21-12 Subepimeria Bellan-Santini, 1972 S. geodesiae AN 2-18 EUEIMNOGAMMARIDAE Berchinia Kamaltynov, 2001 Poekilogammarus curvimanus AN24-15 Barguzinia Kamaltynov, 2001 Abyssogammarus calceolatus AN24-15 Bazikalovia Takhteev, 2001 Microgammarus simplex AN24-24 Sg Lamogammarus Kamaltynov, 2001 Eulimnogammarus macrophthalmus AN24-15 Laxmannia Kamaltynov, 2001 Abyssogammarus swartschewskii AN24-15 Sg Pretiositus Kamaltynov, 2001 Ommatogammarus carneolus melanophthalmus AN24-15 Profundalia Kamaltynov, 2001 Eulimnogammarus tenuis AN24-15 Sluginella Kamaltynov, 2001 Eulimnogammarus pachycerus AN24-15 Tengisia Kamaltynov, 2001 Gammarus capelins AN24-15 EUSIRIDAE Dolobrotus Bowman, 1974 D. mardeni AN 5-25 Frigora Ren, 1991 E ascidicola AN20-30 Luckia Bellan-Santini & Thurston, 1996 E. striki AN21-5 39 Pleusiroides Ortiz, Lalana & Varela, 2007P. alcoladoi AN32-19 Podosirus Bellan-Santini, 2007 P. vaderi AN33-3 Ronconoides Ledoyer, 1973 R. brevicornis AN 3-26 Sennaia Bellan-Santini, 1997 S. bidaetyla AN21-5 Triquetramana Hendrycks & Gonlan, 2003 T brevipalpa AN26-14 EXOEDIGEROTIDAE Exoediceroides Bousfield, 1983 E. maximus Metoediceropsis Dang, 1968 M. dadoensis AN 16- 10 Notoediceros Bousfield, 1983 N. tasmanieus Patuki Gooper & Fineham, 1974 P breviuropodus AN14-40 Vadosiapus Barnard & Thomas, 1988 V eopaeabanus AN 17-7 Warreyus Barnard & Drummond, 1983 Exoedieeros maeulosus AN 15- 15 GAMMARAGANTHIDAE Sg Pseudacanthus Bousfield, 1989 Gammaraeanthus aestuariorum AN 17-22 Relictacanthus Bousfield, 1989 Gammaraeanthus relietus AN 17-22 GAMMAREEEIDAE Austroregia Barnard, 1 989 Atylus huxleyanus AN 17-21 GAMMARIDAE Abludogammarus Karaman, 1980 Gammarus fiavus Accubogammarus Karaman, 1974 Typhlogammarus algor Albanogammarus Ruffo, 1995 A. inguseoi Austrocrangonyx Barnard & Barnard, 1982 Gammarus barringtonensis Austrogammarus Barnard & Karaman, 1983 Gammarus australis Baku Karaman & Barnard, 1979 Pontogammarus paradoxus Cephalogammarus Karaman & Barnard, 1979 Gammarus maerocephalus Comatogammarus Stock, 1971 Sarothrogammarus ferghanensis Compactogammarus Stock, 1974 Niphargoides compactus Condiciogammarus Karaman, 1984 Gammarus retz Gammaropisa Ruffo & Vigna Taglianti, 1988 G. arganoi Jubeogammarus Karaman, 1984 Gammarus alsaticus Kergueleniola Ruffo, 1975 K. macra Kuzmelina Karaman & Barnard, 1979 Gmelina kusnezowi Lagunogammarus Sket, 1971 Gammarus zaddachi Lanceogammarus Karaman & Barnard, 1979 Gammarus andrussowi Laurogammarus Karaman, 1984 Garinogammarus scutarensis Lusigammarus Barnard & Barnard, 1983 Gammarus guernei Obesogammarus Stock, 1974 Gammarus obesus Pallasiola Barnard & Barnard, 1983 Pallasea cancelloides quadrispinosa Paraniphargoides Stock, 1974 Niphargoides motasi Rhipidogammarus Stock, 1971 Gammarus rhipidiophorus Scytaelina Stock, Mirzajani, Vonk, Naderi & Kiabi, 1998 S. simplex Sinogammarus Karaman & Ruffo, 1994/5 S. troglodytes Tadzhikistania Barnard & Barnard, 1983 Sarothrogammarus ruffoi Tadzocrangonyx Karaman & Barnard, 1979 Grangonyx schizurus Turcogammarus Karaman & Barnard, 1979 Obesogammarus turcarum AN 15-30 AN 5-29 AN21-47 AN15-14 AN15-15 AN 12-2 7 AN 12-2 7 AN2-35 AN 5-31 AN 17-41 AN 17-29 AN 17-41 AN 7-28 AN 12-2 7 AN 2-34 AN12 AN 16-20 AN15-14 AN 5-31 AN15-14 AN 5-31 AN 2-35 AN22-62 AN21-28 AN15-14 AN 12-2 7 AN 12-29 40 Tyrrhenogammarus Karaman & Ruffo, 1989 T. sardous AN19-18 Uroniphargoides Stock, 1974 Niphargoides spinieaudatus AN 5-31 Sg Wolgagammarus Stock, 1974 Stenogammarus dzjubani AN 5-31 Yogmelina Karaman & Barnard, 1979 Y limana AN 12-2 7 GAMMAROPOREIIDAE Gammaroporeia Bousfield, 1979 Mieruropus alaskensis AN12-19 HADZIIDAE Afrocrangonyx Karaman, 1981 Metaerangonyx spinieaudatus AN 15-31 Allotexiweckelia Holsinger, 1 980 A. hirsuta AN13 Apoweckelia Stock, 1985 A. serrata AN 17-51 Bahadzia Holsinger & Yager, 1985 B. williamsi AN 17-40 Brachina Barnard & Williams, 1995 B. invasa AN21-4 Sg Caribdzia Stoek, 1985 Metaniphargus nicholsoni AN 17-51 Carinomelita Bousfield, 1990 G. janstocki AN 19-9 Crangoweckelia Stock, 1985 G. spinicauda AN 17-51 Sg Croidzia Stock, 1985 Metaniphargus beattyi AN 17-51 Galapsiellus Barnard, 1976 Paraniphargus leleuporum AN 9-43 Sg Guadzia Stock, 1985 Metaniphargus bullipes AN 17-51 Sg Haidzia Stock, 1985 Metaniphargus plumicauda AN 17-51 Holsingerius Barnard & Karaman, 1982 Texiweekelia samacos AN15-14 Sg Hispadzia Stock, 1985 Metaniphargus longidaetylus AN 17-51 Ilvanella Vigna Taglianti, 1972 L inexpectata AN 3-31 Indoweckelia Holsinger & Ruffo, 2002 L superstes AN24-13 Sgjamadzia Stock, 1985 Metaniphargus jamaieae AN 17-51 May aweckelia Holsinger, 1977 M. yucatanensis AN28-98 Metahadzia Stock, 1977 Hadzia tavaresi AN 10-49 Nedsia Barnard & Williams, 1995 N. douglasi AN21-4 Sg Neoweckelia Dancau, 1973 Weekelia eubanica AN 4-21 Paraholsingerius Sawicki & Holsinger, 2005 Holsingerius smaragdinus AN29-18 Paramexiweckelia Holsinger, 1982 Mexiweekelia particeps AN16-17 Parasalentinella Bou, 1971 P rouehi AN 2-18 Parhadzia Vigna Taglianti, 1 988 P sbordonii AN 17-31 Phreatomelita Ruffo, 1979 P paeeae AN13 Pintoweckelia Stoek, 1985 P grandis AN 17-51 Protohadzia Zimmerman & Barnard, 1977 Eriopisa sehoenerae AN 10-51 Radaweckelia Stoek, 1985 R. brevicauda AN 17-51 Saliweckelia Stock, 1977 S. emarginata AN 10-49 Tamaweckelia Sawicki & Holsinger, 2005 T. apalpa AN29-18 Texiweckelia Holsinger, 1980 Mexiweekelia texensis AN13 Texiweckeliopsis Barnard & Karaman, 1982 Texiweckelia insolita AN15-14 Tuluweckelia Holsinger, 1 990 T eernua AN19-16 Zhadia Eowry & Fenwiek, 1983 Z. subantaretica AN 15-36 Zombiweckelia Stoek, 1985 Z. parvipalpus AN 17-51 HYAEIDAE Apohyale Bousfield & Hendrycks, 2002 Allorehestes pugettensis AN25-3 Sg Boreohyale Bousfield & Hendrycks, 2002 Protohyale lamberti AN25-3 Diplohyale Bousfield & Hendryeks, 2002 Hyale diplodactyla AN25-3 41 Sg Leptohyale Bousfield & Hendrycks, 2002 Protohyale longipalpa AN25-3 Protohyale Bousfield & Hendrycks, 2002 Hyale frequens AN25-3 Ptilohyale Bousfield & Hendrycks, 2002 Allorchestes plumulosus AN25-3 Ruffohyale Bousfield & Hendrycks, 2002 Hyale milloti AN25-3 Serejohyale Bousfield & Hendrycks, 2002 Hyale spinidactyla AN25-3 HYPERIIDAE Laxohyperia Vinogradov & Volkov, 1982 E. vespuliformis AN15-52/53 INGOEFIEEEIDAE Sg Antilleella Rufib & Vigna Taglianti, 1 989 Ingolfiella tabularis AN 17-29 Sg Gevgeliella Stock, 1976 Ingolfiella putealis AN 9-49 Hansenliella Stock, 1981 AN 16-34 Paraleleupia Vonk & Schram, 2003 Trogloleleupia gobabis AN26-35 Proleleupia Vonk & Schram, 2003 Trogloleleupia nudicarpus AN26.35 Rapaleleupia Vonk & Schram, 2007 Trogloleleupia gobabis AN33-25 Stygobarnardia Rufib, 1985 S. caprellinoides AN 17-49 Sg Tethydiella Rufib & Vigna Taglianti, 1989 Ingolfiella fuscina AN 17-29 Sg Trianguliella Stock, 1976 Ingolfiella manni AN 9-49 Trogloleleupia Rufib, 1975 Ingolfiella leleupi AN 7-28 Sg Tyrrhenidiella Rufib & Vigna Taglianti, 1989 Ingolfiella cottarellii AN 17-29 IPANEMIDAE Ipanema Barnard & Thomas, 1988 I. talpa AN 17-7 IPHIMEDIIDAE Anisophimedia Karaman, 1 980 Iphimedia haurakiensis AN 15-31 Coboldus Krapp- Schickel, 1974 G. nitior AN14 Stegopanoploea Karaman, 1980 Panoploea joubini AN 15-31 ISAEIDAE Pagurisaea Moore, 1983 P schembrii AN 15-39 ISGHYROGERIDAE Sg Africoecetes Just, 1983 Goncholestes armatus AN15-29/30 Alatajassa Gonlan, 2007 A. similis AN33-7 Ambicholestes Just, 1998 Garibboecetes magellani AN21-26 Sg Australestesjust, 1998 Ambicholestes berentsae AN21 Sg Australoecetes Just, 1 98 3 Siphonoecetes sellicki AN15-29/30 Bathypoma Eowry & Berents, 1996 B. enigma AN21-34 Baracuma Barnard & Drummond, 1981 B. alquirta AN15-12 Borneoecetes Barnard & Thomas, 1984 B. wongi AN 16-5 Bubocorophium Karaman, 1980 Siphonoecetes tanabensis AN 15-30 Sg Caribboecetes Just, 1983 G. barbadensis AN15-29/30 Sg Centraloecetes Just, 1983 Siphonoecetes kroyeranus AN 15-29 Corocubanus Ortiz & Nazabal, 1984 G. guitarti AN 16-29 Coxischyrocerus Just, 2009 G. rhombocoxus AN34-28 Neoischyrocerus Gonlan, 1995 Microjassa claustra AN21-14 Notopoma Eowry & Berents, 1996 N. stoddartae AN21-34 Sg Orientoecetes Just, 1983 Siphonoecetes orientalis AN 15-29 Paracerapus Budnikova, 1989 Gerapus polikovi AN17-1 Polynesoecetes Myers, 1989 P kekeae AN 17-28 42 Sg Rhinoecetes Just, 1983 R. robustus AN15-29/30 Ruffojassa Vader & Myers, 1996 Parajassa angularis AN21-59 Scutischyrocerus Myers, 1995 S. scutatus AN21-40 Sg Stebbingoecetes Just, 1985 Siphonoeeetes australis AN17-12 Tropischyrocerus Just, 2009 T pugilus AN34-28 Veronajassa Vader & Myers, 1996 V festa AN21-59 IZINKALIDAE Izinkala Griffiths, 1977 L hhla AN 10-41 KAMAKIDAE Aorchoides Eedoyer, 1972 A. dilatata AN 2-28 Gammaropsella Myers, 1 995 G. simplex AN21-40 Heterokamaka Ariyama, 2008 H. isahaya AN33-2 Ledoyerella Myers, 1973 Eembos caputphotis AN 3-42 Natarajphotis Eyla, Velvizhi & Ajmal Khan, 1998 N. manieni AN25-16 Paraloiloi Myers, 1995 P vaga AN21-40 KOTUMSARIDAE Kotumsaria Messouli, Holsinger & Rang; a Reddy, 2007 K. bastarensis AN32-17 KURIIDAE Micropythia Krapp-Sehiekel, 1976 Allorehestes earinatus Pythia Krapp-Sehiekel, 1972 Allorehestes earinatus AN3-25 EAFYSTIIDAE Paralafystius Bousheld, 1987 P meallisteri AN28-97 Protolafystius Bousheld, 1987 P madillae AN28-97 EEPEGHINEEEIDAE Lepechinelloides Thurston, 1980 E. karii AN 12-28 Lepechinellopsis Eedoyer, 1982 E. brevieaudata AN 15-34 EEUGOTHOIDAE Leucothopsis Eedoyer, 1972 AN 2-28 Nepanamixis Thomas, 1997 N. dianthus AN21-57 EIEJEBORGIIDAE Isipingus Barnard & Karaman, 1987 Eiljeborgia epistomata AN 17-6 EUGIOBEIVIIDAE Lucioblivia Tomikawa, 2007 E. kozaensis AN32-27 EYSIANASSIDAE Bonassa Barnard & Karaman, 1991 Eysianassa bonairensis AN 19-5 Bruunosa Barnard & Karaman, 1987 Tryphosa bruuni AN 17-6 Caeconyx Barnard & Karaman, 1991 Tmetonyx eaeeulus AN 19-5 Concarnes Barnard & Karaman, 1991 Soearnes eoneavus AN 19-5 Conicostoma Eowry & Stoddart, 1983 G. karta AN 15-36 Coximedon Barnard & Karaman, 1991 Gheirimedon latimanus AN 19-5 Dartenassa Barnard & Karaman, 1991 Eysianassa dartevellei AN 19-5 43 Dissiminassa Barnard & Karaman, 199] L Aruga dissimilis AN 19-5 Eclecticus Lowry & Stoddart, 1997 E. eclecticus AN22-38 Falcanassa Barnard & Karaman, 1991 Eysianassa falcata AN 19-5 Falklandia De Broyer, 1985 Orchomenopsis reducta AN17-36 Gronella Barnard & Karaman, 1991 Anonyx groenlandicus AN 19-5 Kakanui Lowry & Stoddart, 1983 K. punui AN 15-36 Lepiduristes Barnard & Karaman, 1987 Uristes lepidus AN 17-6 Lucayarina Clark & Barnard, 1985 E. catacumba AN 16-9 Macronassa Barnard & Karaman, 1991 Aruga macromerus AN 19-5 Sg Orchomenyx De Broyer, 1984 Orchomenella macronyx AN16-10 Orenoquia Bellan-Santini, 1997 O. serrata AN21-5 Ottenwalderia Jaume & Wagner, 1998 O. kymbalion AN22-28 Pardia Ruffo, 1987 Gallisoma punctatum AN17-17 Rhinolabia Ruffo, 1972 R. parthenopeia AN 3-29 Rimakoroga Barnard & Karaman, 1987 Pseudokoroga rima AN 17-6 Riwo Lowry & Stoddart, 1995 R. mizeui AN21 Scopolostoma Lowry & Stoddart, 1983 Stomacontion prionoplax AN 15-36 Septcarnes Barnard & Karaman, 1991 Socarnes septimus AN 19-5 Tantena Ortiz, Lalana & Varela, 2007 T zladarkii AN32-19 Thaumodon Lowry & Stoddart, 1995 T poorei AN21-34 Ventiella Barnard & Ingram, 1 990 V sulfuris AN 19-8 Wecomedonjarrett & Bousfield, 1982 Hippomedon wecomus AN 15-29 MAERIDAE Anamaera Thomas & Barnard, 1985 A. hixoni AN 16-36 Austromaera Lowry & Springthorpe, 2005 Megamaera mastersii AN31-18 Ceradomaera Ledoyer, 1973 G. plumosa AN 3-26 Clessidra Krapp-Schickel & Vader, 2009 Maera tinkerensis AN34-32 Coxomaerella Karaman, 1981 G. pirloti AN 15-31 Sg Dentelasmopus Ledoyer, 1982 Elasmopus spinipalpus AN15-34/5 Dumosus Thomas & Barnard, 1985 D. atari AN 16-36 Glossomaera Krapp-Schickel, 2009 Maera octodens AN34-32 Hamimaera Krapp-Schickel, 2008 Maera hamigera AN33-14 Hoho Lowry & Fenwick, 1983 Mallacoota marilla AN 15-36 Jerbarnia Croker, 1971 J. macrochira AN 2-19 Linguimaera Pirlot, 1936 E. pirloti AN26-20 Lupimaera Barnard & Karaman, 1982 Maera lupana AN15-14 Maeracoota Myers, 1997 M. tridentata AN21-40 Megaceradocus Mukai, 1979 M. gigas AN 12-30 Miramaera Eowry & Springthorpe, 2005 M. thetis AN31-18 Otbomaera Krapp-Schickel, 2001 Gammarus othonis AN23-30 Pseudelasmopus Ledoyer. 1978 P cheliferus AN 10-44 Quadrimaera Krapp-Schickel & Ruffo, 2000 Gammarus quadrimanus AN22-34 Ruffomaera Krapp-Schickel, 2008 Maera williamsi AN33-14 Sauradocus Yerman & Krapp-Schickel, 2009 S. hobbit Spatbiopus Thomas & Barnard, 1985 S. looensis AN 16-36 Wimvadocus Krapp-Schickel & Jarrett, 2000 Geradocus torelli AN22-33 Zygomaera Krapp-Schickel, 2001 Maera eugeniae AN23-30 MAXILLIPIIDAE Maxillipides Ledoyer, 1984 M. laticarpus AN 16-2 2 Maxillipius Ledoyer, 1973 M. rectitelson AN 3-26 44 MEGALANGEOLIDAE Megalanceoloides Zeidler, 2009 Eanceola remipes AN 34-60 MEGAEUROPIDAE Gibberulus Thomas & Barnard, 1986 Megaluropus longimerus AN17-52 Resupinus Thomas & Barnard, 1986 R. spinicaudatus AN17-52 MEEITIDAE Abludomelita Karaman, 1981 Melita gladiosa AN 15-31 Allomelita Stock, 1984 Melita pellucida AN 16-34 Alsacomelita Karaman, 1984 A. semipalmata AN 17-41 Anchialella Barnard, 1979 A. vulcanella AN 11-34 Animoceradocus Karaman, 1984 Megamoera semiserrata AN 17-42 Caledopsis Stock & Iliffe, 1995 G. levis AN21-54 Cephalopisella Karaman, 1984 Eriopisella propagatio AN 17-42 Confodiopisa Karaman, 1984 Psammogammarus caesicolus AN17-41 Cottesloe Barnard, 1974 AN 4-30 Desdimelita Bousheld & Ghevrier, 1996 Melita desdichada AN21-25 Fiha Stock, 1988 E schminkei AN17-15 Flagitopis a Karaman, 1984 Niphargus philippensis AN 17-41 Giniphargus Karaman & Barnard, 1979 Niphargus pulchellus AN 12-2 7 Impertiopis a Karaman, 1984 Eriopisa gracilis AN17-41/2 Josephosella Ruffo, 1985 J. andamana AN 17-49 Madapisella Stock, 1980 Eriopisella madagascarensis AN13 Maleriopa Barnard & Karaman, 1982 Eriopisella dentifera AN15-14 Megamoera Sp. Bate, 1862 Gammarus dentatus AN21-25 Nainaloa Karaman & Barnard, 1979 Melita latimera AN 12-2 7 Nippopisella Stock, 1980 Eriopisella nagatai AN13 Norcapensis Bradbury & Williams, 1997 N. mandibulis AN21-11 Nurina Bradbury & Eberhard, 2000 N. poulteri AN22-8 Psammomelita Vonk, 1988 P uncinata AN17-31 Quadrus Karaman, 1984 Q vagabundus AN 17-42 Quasimelitajarrett & Bousheld, 1996 Melita quadrispinosa AN21-25 Roropis a Karaman, 1984 Victoriopisa atlantica AN17-41/2 Rotomelita Barnard, 1977 R. lokoa AN 10-3 7 Sriha Stock, 1989 Quadrus vagabundus AN17-15 Spiniferopisella Karaman, 1984 Eriopisella spinosa AN 17-42 Tabatzius McKinney & Barnard, 1977 T copillius AN 10-45 Tagua Eowry & Fenwick, 1983 T sporema AN 15-36 Tegano Barnard & Karaman, 1982 Melita seticornis AN15-14 Thalassostygius Vonk, 1 990 Th. exiguus AN 19-30 Tunisopisa Stock, 1980 Eriopisa seurati AN Valettiella Griffiths, 1977 V castellana AN 10-41 Verdeia Eowry & Springthorpe, 2007 Melita grandimana AN32-15 Vicitopisa Karaman, 1984 Eriopisa inaequicaudata AN 17-41 Victoriopisa Karaman & Barnard, 1979 Niphargus chilkensis AN 12-2 7 MEEPHIDIPPIDAE Melphisubchela Andres, 1981 M. prehenda AN15-11 MESOGAMMARIDAE Octopupilla Tomikawa, 2007 O. felix AN32-27 Paramesogammarus Bousheld, 1979 P americanus AN12-19 45 METAGRANGONYGTIDAE Longipodocrangonyx Boutin & Messouli, 1988 E. maroccanus AN 17-8 Pygocrangonyx Karaman & Barnard, 1979 Metacrangonyx remyi AN 12-2 7 MIRAMARASSIDAE Miramarassa Ortiz, Ealana & Eio, 1999. M. sanchezi AN23-41 MIGRUROPODIDAE Linevichella Kamaltynov, 2001 Gammarus vortex AN24-15 NAJNIDAE Carinonajna Bousfield & Marcoux, 2004 G. bicarinata AN27-5 NEOMEGAMPHOPIDAE Maragopsis Myers, 1973 Eemboides bidentata AN 3-42 Riwomegamphopus Myers, 1995 R. bamus AN21-40 Varohios Barnard, 1979 V topianus AN 11-34 NEONIPHARGIDAE Jasptorus Bradbury & Williams, 1997 J. solepti AN21-11 Neocrypta Bradbury & Williams, 1997 N. primaris AN21-11 Tasniphargus Williams & Barnard, 1 988 T. tyleri AN 17-5 Wesniphargus Williams & Barnard, 1988 Neoniphargus nichollsi AN 17-5 Wombeyanus Bradbury & Williams, 1997 W botulosus AN21-11 Yulia Wiliams & Barnard, 1988 Neoniphargus yuli AN 17-5 NIHOTUNGIDAE Nihotunga Barnard, 1972 N. iluka AN 3-39 NIPHARGIDAE Foroniphargus Karaman, 1985 E pori AN 17-42 Niphargobates Sket, 1981 N. orophobata AN 15-48 OGHEESIDAE Curidia Thomas, 1983 G. debrogania AN 15-51 Meraldia Barnard & Karaman, 1987 Ochlesis meraldi AN 17-6 ODIIDAE Antarctodius Berge, Vader & Goleman, 1999 Odius antarcticus AN22-5 Cryptodius Moore, 1992 Odius kelleri AN20-25 Imbrexodius Moore, 1992 L oclairi AN20-25 Postodius Hirayama, 1983 P imperfectus AN 15-2 7 OEDIGEROTIDAE Aborolobatea Eedoyer, 1984 A. paracheliformis AN 16-2 2 Americhelidium Bousfield & Ghevrier, 1996 Synchelidium spinipes AN21-8 Americulodes Bousfield & Ghevrier, 1 996 Monoculodes edwardsi AN21-8 Cavoplaxus Ren, 1992 G. jiaozhouwanensis AN28-99 Chitonomandibulum Jo, 1 990 G. emargicoxa AN 17-24 Cornudilla Barnard & Karaman, 1991 Westwoodilla cornuta AN 19-5 46 Deflexilodes Bousfield & Chevrier, 1996 Monoculodes tenuirostratus AN21-8 Eochelidium Bousfield & Chevrier, 1 996 Synchelidium lenorostratum AN21-8 Finoculodes Barnard, 1971 E omnifera AN2-17 Hartmanodes Bousfield & Chevrier, 1996 Monoculodes hartmannae AN21-8 Hongkongvena Hirayama, 1992 H. memoria AN20-14 Piroyera Sp.Bate, 1857 Monoculodes carinatus AN21-8 Limnoculodes Bousfield & Chevrier, 1996 Monoculodes limnophilus AN21-8 Machaironyx Coyle, 1980 M. muelleri AN 15-20 Pacifoculodes Bousfield & Chevrier, 1996 Monoculodes spinipes AN21-8 Paramonoculopsis Alonso de Pina, 1997 P. acuta AN21-1 Parexoediceros Bousfield, 1983 P latimerus Rostroculodes Bousfield & Chevrier, 1996 Monoculodes longirostris AN21-8 PACHYNIDAE Acheronia Lowry, 1 984 A. pegasus AN 16-2 3 Coriolisa Lowry & Stoddart, 1994 G. caledonica AN27-37 Drummondia Lowry, 1 984 D. corinellae AN 16-2 3 Ekelofia Lowry, 1 984 Pachychelium oculatum AN16-23/4 She ardella Lowry, 1984 S. kapala AN 16-2 3 PALLASEIDAE Babr Kamaltynov & Vainola, 2001 Gammarus lovenii Dybowsky AN24-15 Burchania Takhteev, 2000 Hakonboeckia meissneri AN24-25 Pallaseopsis Kamaltynov & Vainola, 2001 Gammarus grubii AN24-15 PARAGALLIOPIIDAE Doowia Barnard & Drummond, 1987 D. cooma AN 17-6 Indocalliope Barnard & Karaman, 1982 Paracalliope indica AN15-14 Katocalliope Barnard & Drummond, 1 984 K. kutyeri AN 16-5 Yhi Barnard & Thomas, 1991 Y. yindi AN20-2 PARAGERGOPIDAE Paracercops Vassilenko, 1972 P setifer AN 3-38 Pseudocercops Vassilenko, 1972 P kussakini AN 3-38 PARAGAMMAROPSIDAE Paragammaropsis Ren, 1991 P prenes AN20-30 PARALEPTAMPHOPIDAE Ringanui Fenwick, 2006 Calliope subterraneus AN31-8 Rudolphia Grosso & Peralta, 2009 R. macrodactylus AN34-21 PARAMELITIDAE Antipodeus Williams & Barnard, 1988 Gammarus antipodeus AN 17-5 Aquadulcaris Stewart & Griffiths, 1995 Gammarus crassicornis AN21-53 Chillagoe Barnard & Williams, 1995 G. thea AN21-4 Chydaekata Bradbury, 2000 G. acuminata AN22-8 I^uptus Finston, Johnson & Knott, 2008 K. linnaei ??? 47 Mathamelita Stewart & Griffiths, 1995 M. aequidentata AN21-53 Molina Bradbury, 2000 M. pleobranchos AN Pilbarus Bradbury & Williams, 1997 P mil] si AN21-11 Totgammarus Bradbury & Williams, 1995 T eximius AN21-11 Toulrabia Barnard & Williams, 1995 T willsi AN21-4 PARDALISGIDAE Andeepia Biswas, Coleman & Hendrycks, 2009 A. ingridae AN34-6 Antronicippe Stock & Iliffe, 1 990 A. serrata AN 17-58 Caleidoscopsis Karaman, 1974 Pardaliscopsis copal AN 5-28 Macroarthrus Hendrycks & Gonlan, 2003 M. victoriae AN26-14 Octomana Hendrycks & Gonlan, 2003 O. hadromischa AN26-14 Rhynohalicella Karaman, 1974 Halicella halona AN 5-28 Spelaeonicippe Stock & Vermeulen, 1982 S. provo AN 15-50 PHOTIDAE Corogammaropsis Tzvetkova, 1990 G. kudrjaschovi AN27-39 Dodophotis Karaman, 1986 Photis digitata AN 17-42 Falcigammaropsis Myers, 1995 E excavata Graciliphotis Myers, 2009 G. ruthae AN34-41 Latigammaropsis Myers, 2009 Gammaropsis atlantica AN34-41 Papuaphotis Myers, 1995 P regis AN21-40 Posophotis Barnard, 1979 P seri AN 11-34 Pseudophotis Hirayama, 1984 P ariakensis AN16-16 Rocasphotis Souza-Filho & Serejo, 2010 R. also AN34-51 Virgammaropsis Myers, 2009 V artemis AN34-42 PHOXOGEPHAEIDAE Baliphoxus Ortiz & Ealana, 1999 B. andresi AN22-49 Basuto Barnard & Drummond, 1978 Pontharpinia stimpsoni ANll-21 Bathybirubius Senna, 2010 B. margaretae AN34-49 Beringiophoxus Jarrett & Bousheld, 1994B. beringianus AN20-16 Birubius Barnard & Drummond, 1976 B. panamunus AN 8-18 Booranus Barnard & Drummond, 1978 B. weemus AN 11-20 Brolgus Barnard & Drummond, 1978 Paraphoxus tattersalli AN 11-20 Cephalophoxoides Gurjanova, 1977 Phoxocephalus bassi ANll-14 Cephalophoxus Gurjanova, 1977 Phoxocephalus regium ANll-14 Cocoharpinia Karaman, 1980 G. iliffei AN 15-30 Cunmurra Barnard & Drummond, 1978 G. itickerus AN 11-20 Diogodias Barnard & Drummond, 1978 Metaphoxus longicarpus ANll-21 Elpeddo Barnard & Drummond, 1978 E. kaikai AN 11-20 Eobrolgus Barnard, 1979 Paraphoxus spinosus AN12-17 Eusyrophoxus Gurjanova, 1977 Parharpinia calcarata AN12-17 Feriharpinia Barnard & Karaman, 1982 Harpinia ferentaria AN15-14 Foxiphalus Barnard, 1979 Pontharpinia obtusidens AN12-17 Fuegiphoxus Barnard & Barnard, 1980 Parharpinia fuegiensis AN13 Ganba Barnard & Drummond, 1978 G. pellati AN 11-20 Grandiphoxus Barnard, 1979 Phoxus grandis AN12-17 Griffithsius Jarrett & Bousheld, 1994 Mandibulophoxus latipes AN28-98 Hopiphoxus Barnard & Drummond, 1978 Metaphoxus simillimus ANll-21 Indophoxus Dang & Ee, 2005 L curvirostris AN29-5 Japara Barnard & Drummond, 1978 J. papporus ANll-21 Jerildaria Barnard & Drummond, 1978 J. joubiphoxus ANll-21 Kondoleus Barnard & Drummond, 1978 K. tekin ANll-21 48 Kotla Barnard & Drummond, 1978 K. batturi Kulgaphoxus Barnard & Drummond, 1978 K. borralis Kuritus Barnard & Drummond, 1978 K. nacoomus Leongathus Barnard & Drummond, 1978L. nootoo Linca Alonso de Pina, 1993 L. pinita Majoxiphalus Jarre tt & Bousfield, 1994 Foxiphalus major Matong Barnard & Drummond, 1978 M. matong Mesophoxus Gurjanova, 1977 M. laperusi Palabriaphoxus Gurjanova, 1977 Harpinia palabria Parafoxiphalus Alonso de Pina, 2001 P longicarpus Parajoubinella Gurjanova, 1977 Phoxocephalus concinna Paramesophoxus Gurjanova, 1977 P rakumae ?? Parametaphoxus Gurjanova, 1977 Phoxocephalus fultoni Phoxorgia Barnard & Barnard, 1980 Parharpinia sinuata Pseudfoxiphalus Andres, 1991 P setosus Rhepoxynius Barnard, 1979 Pondiarpinia epistoma Rikkarus Barnard & Drummond, 1978 R. lea Ringaringa Barnard & Karaman, 1991 Metaphoxus littoralis Synphoxus Gurjanova, 1980 S. novaezealandicus Tickalerus Barnard & Drummond, 1978 T birubi Tipimegus Barnard & Drummond, 1978 T thalerus Torridoharpinia Barnard & Karaman, 1982 Proharpinia hurleyi Uldanamia Barnard & Drummond, 1978 U. pillare Urophoxus Gurjanova, 1977 Urothoe pinguis Vasco Barnard & Drummond, 1978 Metaphoxus brevidactylus Vietophoxus Dang & Le, 2005 V longrostris Waipirophoxus Gurjanova, 1980 Paraphoxus waipiro Waitangi Fincham, 1977 Paraphoxus rakiura Wildus Barnard & Drummond, 1978 W thambaroo Yammacoona Barnard & Drummond, 1978 Y kunarella Yan Barnard & Drummond, 1978 Y. tiendi PHOXOGEPHALOPSIDAE Eophoxocephalopsis Thurston, 1989 E. rhachianensis Puelche Barnard & Clark, 1982 P orenzani PHREATOGAMMARIDAE Caledonietta lannilli & Ruffo, 2007 G. maryae Ruf&a Brehier, Vonk &Jaume, 2010 R. patagonica PEATYISGHNOPIDAE Eudevenopus Thomas & Barnard, 1983 Platyischnopus metagracilis Indischnopus Barnard & Drummond, 1979 Platyischnopus herdmani Skaptopus Thomas & Barnard, 1983 S. brychius Tiburonella Thomas & Barnard, 1983 Platyischnopus viscana Tittakunara Barnard & Drummond, 1979 T katoa Tomituka Barnard & Drummond, 1979 T doowi Yurrokus Barnard & Drummond, 1979 Y cooroo PEEUSTIDAE Anomalosymtes Hendrycks & Bousheld, 2004 A. coxalis Budnikopleustes Hendrycks & Bousheld, 2004 Pleusymtes vasinae Sg Catapleustes Bousheld & Hendrycks, 1994 Pleustes victoriae Chromopleustes Bousheld & Hendrycks, 1 995 ANll-21 ANll-21 AN 11-20 AN 11-20 AN20-1 AN20-16 AN 11-20 ANll-14 ANll-14 AN23-1 ANll-14 ANll-14 ANll-14 AN13 AN20-1 AN12-17 ANll-21 AN 19-5 AN13 ANll-21 AN 11-20 AN15-14 ANll-21 ANll-14 ANll-21 AN29-5 AN13 AN 9-56 AN 11-20 AN 11-20 ANll-21 AN 17-31 AN15-13 AN32-12 AN34-7 AN 15-51 AN12-18 AN15-51 AN 15-51 AN12-18 AN12-18 AN12-18 49 AN27-14 AN27-14 AN28-97 Parapleustes oculatus AN21-9 Commensipleustes Bousfield & Hendrycks, 1995 Parapleustes commensalis AN21-9 Dactylopleustes Karaman & Barnard, 1979 Parapleustes echinoicus AN 12-26 Eosymtes Bousfield & Hendrycks, 1 994 E. minutus AN20-4 Gnathopleustes Bousfield & Hendrycks, 1995 Iphimedia pugettensis AN21-9 Gracilipleustes Hendrycks & Bousfield, 2004 Sympleustes gracilis AN27-14 Heteropleustes Hendrycks & Bousfield, 2004 H. setosus AN27-14 Holopleustes Hendrycks & Bousfield, 2004 H. aequipes AN27-14 Inciso calliope Bousfield & Hendrycks, 1 995 L newportensis AN21-9 Kamptopleustes Hendrycks & Bousfield, 2004 K. spinosus AN27-14 Micropleustes Bousfield & Hendrycks, 1995 Parapleustes nautilus AN21-9 Myzotarsa Gadien & Martin, 1999 M. anaxiphilia AN22-9 Rhinopleustes Hendrycks & Bousfield, 2004 R. acuminatus AN27-14 Shoemakeroides Hendrycks & Bousfield, 2004 Sympleustes cornigera AN27-14 Tepidopleustes Karaman & Barnard, 1979 Parapleustes barnardi AN12-27 Thorlaksonius Bousfield & Hendrycks, 1 994 T. brevirostris AN28-97 Trachypleustes Bousfield & Hendrycks, 1995 T. trevori AN21-9 PODOGERIDAE Neoxenodice Eowry 1976 N. cryophila AN8-24 Podobothrus Barnard & Clark, 1985 P bermudensis AN17-33 Styloxenodice Eaubitz, 1983 Xenodice macrophthalma AN15-33/4 PONTOGENEIIDAE Abdia Barnard & Karaman, 1987 Atylopsis latipalpus AN 17-6 Antarctogeneia Thurston, 1974 A. macrodactyla AN6-23 Sg Ganigamoera Sidorov, 2009 Paramoera myslenkovi AM34-50 Haliogeneia Eowry & Stoddart, 1 998 H. crosnieri AN22-38 Sg Humilomoera Staude, 1 995 Paramoera leucophthalma AN21-52 Inhaca Ortiz, Berze-Freire & Wasikete, 1990 L gnatholobata AN20-27 Manerogeneia Barnard & Karaman, 1987 Pontogeneiella maneroo AN17-6 Sg Moonamoera Staude, 1995 Paramoera rua AN21-52 Nasageneia Barnard & Karaman, 1982 Pontogeneia nasa AN15-14 Relictomoera Barnard & Karaman, 1982Paramoera relicta AN15-14 Sg Rhithromoera Staude, 1995 Paramoera carlottensis AN21-52 Sternomoera Barnard & Karaman, 1982 Paramoera yezoensis AN15-14 Whangarusa Barnard & Karaman, 1987 Panoploea translucens AN 17-6 PONTOPOREIIDAE Diporeia Bousfield, 1989 Pontoporeia hoyi AN17-22 Monoporeia Bousfield, 1989 Pontoporeia affinis AN17-22 PRISGOMIEITARIDAE Paraphotis Ren, 1997 P sinensis AN22-54 Priscomilitaris Hirayama, 1988 P tenuis AN 17-3 PROSGINIDAE Cheloscina Shih & Hendrycks, 1996 G. antennata AN2 1-50/1 PROTOMEDEIINAE Cylindromolaris Ortiz & Ealana, 1 999 Gheiriphotis quadrichelata AN22-49 Pareurystheus Tzvetkova, 1977 Eurystheus anamae ANll-18 Pumiliophotis Myers, 2009 P queenslandicus 50 PSEUDONIPHARGIDAE Parapseudoniphargus Notenboom, 1988 P baetis AN17-16 RAKIROIDAE Rakiroa Eowry & Fenwick, 1982 R. rima AN 15-36 SGINIDAE Spinoscina Bowman & Gruner, 1973 Acanthoscina spinosa AN4-20 SGOPEEOGHEIRIDAE Anisocallisoma Hendrycks & Gonlan, 2003 A. armigera AN26-14 SEBIDAE Caribseba Shaw, 1989 Seba tropica AN20-32 Relictoseborgia Karaman, 1982 Seborgia relicta AN 15-3 2 SIGAFODIIDAE Sicafodia Just, 2004 S. stylos AN27-17 SINUROTHOIDAE Sinurothoe Ren, 1999 S. sinensis AN22-54 STEGOGEPHAEIDAE Alania Berge & Vader, 2001 Stegocephaloides calypsonis AN23-5 Austrocephaloides Berge & Vader, 2001 Stegocephaloides australis AN23-5/6 Austrophippsia Berge & Vader, 2001 Phippsia unihamata AN23-6 Bouscephalus Berge & Vader, 2001 Stegocephalopsis mamillidacta AN23-6 Gordania Berge & Vader, 2001 Phippsiella minima AN23-6 Glorandaniotis Eedoyer, 1986 G. fissicaudata AN 17-43 Mediterexis Berge & Vader, 2001 Andaniexis mimonectes AN23-5 Pseudo Berge & Vader, 2001 Phippsiella pseudophippsia AN23-6 Schellenbergia Berge & Vader, 2001 Stegocephaloides vanhoeffeni AN23-6 Stegocephalexia Moore, 1992 S. penelope AN20-25 Stegomorphia Berge & Vader, 2001 Phippsiella watlingi AN23-6 Stegonomadia Berge & Vader, 2001 Stegocephalina biofar AN23-6 Stegosoladius Barnard & Karaman, 1987Andaniotes simplex AN 17-6 Stegophippsiella Bellan-Santini & Eedoy ^er, 1974 S. pads AN 5-32 STERNOPHYSINGIDAE Sternophysinx Holsinger & Straskraba, 1973 AN 4-23 STENOTHOIDAE Aurometopa Barnard & Karaman, 1987 Metopoides aurorae AN 17-6 Chucullba Barnard, 1974 G. alia AN 4-30 Hardametopa Barnard & Karaman, 1991Metopa nasuta AN 19-5 PGiysmetop a Barnard & Karaman, 1987 Parametopa grandimana AN 17-6 Paraprobolisca Ren, 1991 P leptopoda AN20-30 Pycnopyge Krapp- Schickel, 2000 Prothaumatelson carinatum AN22-33 Raumahara Barnard, 1972 R. dertoo AN 3-39 Sandrothoe Krapp- Schickel, 2006 S. distans AN31-15 Scaphodactylus Rauschert & Andres, 1 994 S. simus AN21-45 Synkope laurina Krapp-Schickel, 1999 S. laurina AN22-33 51 Thaumatelsonella Rauschert & Andres, 1 990 T. kingelepha AN 19-24 Torometopa Barnard & Karaman, 1987 Metopa crenatipalmata AN 17-6 Verticotelson Krapp-Schickel, 2006 V mantis AN31-15 Vonimetopa Barnard & Karaman, 1987 Metopella dubia AN 17-6 Wallometopa Barnard, 1974 W. cabon AN 4-30 Yarra Krapp-Schickel, 2000 Y. unguiserra AN22-33 Zaikometopa Barnard & Karaman, 1987 Metopelloides erythrophthalmus AN17-6 STILIPEDIDAE Bathypanoploea Holman & Wading, 1983 B. schellenbergi AN 5 SYNOPIIDAE Ileraustroe Barnard, 1972 Austrosyrrhoe ilergetes AN 3-39 Latacunga Barnard, 1972 E. latacunga AN 3-39 Me tatiron Rabindranath, 1972 Pseudotiron brevidactylus AN 2-32 Priscosyrrhoe Barnard, 1972 Austrosyrrhoe priscis AN 3-39 Sg Telsosynopia Karaman, 1986 Synopia variabilis AN17-13 TAEITRIDAE Agilestia Friend, 1982 A. hyperocha AN 15-24 Americorchestia Bousheld, 1991 Orchestia longicornis AN 19-9 Atlantorchestia Serejo, 2004 Pseudorchestoidea brasiliensis AN27-29 Australorchestia Serejo & Eowry, 2008 A. occidentalis AN33-22 Austrotroides Friend, 1982 A. pectinalis AN 15-24 Bello rchestia Serejo & Eowry, 2008 B. richardsoni AN33-22 Bousfieldia Chou & Fee, 1996 B. phoenixae AN25-5 Brevitalitrus Bousheld, 1971 Talitrus hortulanus AN 2-19 Cariborchestia Smith, 1998 G. xerophila AN22-59 Caribotroides Bousheld, 1984 G. jamaicensis AN 16-7 Cerrorchestia Eindeman, 1990 G. hyloraina AN 19-20 Chelorchestia Bousheld, 1984 Orchestia costaricana AN 16-7 Chiltonorchestia Bousheld, 1984 Parorchestia pusilla AN16-7 Chroestia Marsden & Fenwick, 1984 G. lota AN16-25 Cochinorchestia Eowry & Peart, 2010 Parorchestia notabilis AN34-36 Dana Eowry, 2011 Deshayesorchestia Ruffo, 2003 Orchestia deshayesii AN 26-33 Eorchestia Bousheld, 1984 Orchestia rectipalma AN 16-7 Floresorchestia Bousheld, 1984 Orchestia horesiana AN 16-7 Hawaiorchestia Bousheld, 1984 Orchestia hawaiensis AN 16-7 Kanikania Duncan, 1994 Parorchestia improvisa AN25-7 Macarorchestia Stock, 1989 M. martini AN 17-30 Makawe Duncan, 1 994 Orchestia hurleyi AN25-7 Sg Mexitroides Eindeman, 1990 Garibotroides pecki AN 19-20 Microrchestia Bousheld, 1984 Parorchestia macrochela AN16-7 Notorchestia Serejo & Eowry, 2008 N. lobata AN33-22 Paciforchestia Bousheld, 1982 Parorchestia klawei AN15-17 Palmorchestia Stock & Martin, 1 988 P hypogaea AN17-18 Platorchestia Bousheld, 1982 Orchestia platensis AN15-17 Protaustrotroides Bousheld, 1984 P victoriae AN 16-7 Protorchestia Bousheld, 1982 Orchestia nitida AN15-17 Pseudorchestoidea Bousheld, 1982 Orchestoidea biolleyi AN15-17 Puhuruhuru Duncan, 1994 P aotearoa AN25-7 Sardorchestia Ruffo, 2003 Talorchestia pelecaniformis AN26-33 Sinorchestia Miyamoto & Morino, 1 999 Talorchestia sinensis AN22-43 52 Tara Duncan, 1994 Orchestia sylvicola AN25-7 Tethorchestia Bousfield, 1984 T antillensis AN 16-7 Transorchestia Bousfield, 1982 Orchestia chiliensis AN15-17 Traskorchestia Bousfield, 1982 Orchestia traskiana AN15-17 Uhlorchestia Bousfield, 1984 Orchestia uhleri AN 16-7 Waematau Duncan, 1 994 W. manawatahi AN25-7 TEMNOPHLIANTIDAE Hystriphlias Barnard & Karaman, 1987 Temnophlias hystrix AN 17-6 THORIEEEIDAE Parachevreuxiella Andres, 1987 P. lobata AN 17-6 THURSTONEEEIDAE Thurstonella Eowry & Zeidler, 2008 Glarencia chelata AN33-16 TUEEARIDAE Tulearus Eedoyer, 1979 T thomassini AN13 UNGIOEIDAE Dactylocorophium Karaman, 1980 Unciola obliquua AN 15-30 Janice Griffiths, 1973 J. spinidactyla AN 3-25 Liocuna Myers, 1981 E. caeca AN 16-28 Orstomia Myers, 1998 O. kanakia AN22-47 Pedicorophium Karaman, 1981 Unciola laminosa AN 15-30 Pterunciolajust, 1977 P. spinipes AN 10-42 Ritaumius Eedoyer, 1978 R. longicornis AN 10-44 Wombalano Thomas & Barnard, 1991 W. yerang AN20-36 Zoedeutopus Barnard, 1979 Z. cinaloanus AN 11-34 URISTIDAE Cedrosella Barnard & Karaman, 1987 Ambasiopsis fomes AN 17-6 Cicadosa Barnard & Karaman, 1987 Anonyx cicadoides AN 17-6 Dounialella Eedoyer, 1986 D. longichelata AN 17-43 Galathella Barnard & Karaman, 1987 Schisturella galatheae AN 17-6 Gippsia Eowry & Stoddart, 1995 G. jonesae AN21 Martensia Barnard & Karaman, 1991 Eysianassa martens! AN 19-5 Nagada Eowry & Stoddart, 1995 N. uwedoi AN21-34 Parschisturella Andres, 1983 P simplex AN15-12 Pseudonesimoides Bellan-Santini & Eedoyer, 1974 P cornutilabris AN 5-32 Stephonyx Eowry & Stoddart, 1 989 Euonyx biscayensis AN 17-56 UROHAUSTORIIDAE Dirimus Barnard & Drummond, 1982 D. tarlitus AN 15-13 Gheegerus Barnard & Drummond, 1982 G. garbaius AN 15- 13 Huarpe Barnard & Clark, 1982 H. escofeti AN 15- 13 Narunius Barnard & Drummond, 1982 N. tallerkus AN 15- 13 Nepella Barnard & Drummond, 1991 N. nelera AN20-2 To ttungus Barnard & Drummond, 1982 T. tungus AN 15- 13 Tuldarus Barnard & Drummond, 1982 T cangellus AN 15-13 Warragaia Berents, 1985 W. rintouli AN 16-6 53 Amphipod newsletter 36 UROTHOIDAE Cunicus Griffiths, 1974 G. profundus AN 5-27 Pseudurothoe Ledoyer, 1986 P. benthedii AN 17-43 VALETTIOPSIDAE Valettietta Eincoln & Thurston, 1983 V lobata AN 15-35 VIBIEIIDAE Vibilioides Ghevreux, 1905 AN26-37 VIGMUSIIDAE Acanthonotozomopsis Watling & Holman, 1980 Acanthonotozomella pushkini AN13 Vicmusiajust, 1990 V duplocoxa AN 18-5 WANDINIDAE Pseudocyphocaris Eedoyer, 1986 P coxalis AN 17-43 Wandin Eowry & Stoddart, 1 990 W. griffini AN 19-20 ZOBRAGHOIDAE Bumeralius Barnard & Drummond, 1982B. buchalius AN15-13 Chono Glark & Barnard, 1987 G. angustiarum AN17-35 Prantinus Barnard & Drummond, 1982 P talanggi AN15-13 Tonocote Glark & Barnard, 1988 T.magellani AN17-35 Incertae sedis Sensonator Notenboom, 1986 S. valentiensis AN 17-47 54 Amphipod newsletter 36 FEATURE INTERVIEW 2012 Wim Voder Early on and just after starting school (despite WW2 going on), Wim knew he wanted to study biology. His father, whom was the Mayor of their village wished differently for Wim, hoping that he would study something other than biology and that would eventually lead to a good career. At 12 years old, Wim got involved with a youth nature study group in Holland (Nedelandse Jeugdbond voor Natuurstudie). With this group Wim hiked all over Holland having the opportunity to explore beaches and study plants. His love for nature, particularly for flowers, began then. His 20 km bike ride to high school allowed him to increase his knowledge of plants while teaching his friend Riet (whom has now been Wim’s partner for the last 20 years) about them as well. One could say this was Wim’s beginnings as a systematist and teacher! Wim was the first in his family to attend University. During this time, Wim worked teaching and research assistant. When and why did Wim start studying amphipods? As a beginning student Wim was a member of Beach study group (Strand Werk Groep). He had asked an older student what to study. It was suggested Wim should have a look at amphipods, since “nobody” was interested in them anyway. Since then, “that was that.” Half of Wim’s Master’s degree research was on Bathyporeia (1 year). The other half not surprisingly, was on plants. Wim also worked 2 years as benthos zoologist at the Delta Institute (Yerseke, Holland). In 1965, Wim was awarded a University funded graduate student stipend that allowed him 5 years of study at the University of Bergen. Wim eventually became a research scholar (Norwegian Research Foundation- funded) for some years (UiB). His work involved a project on the ecology of Marinogammarus. Rumors were that “somebody in Scotland” was working on this genus, so he changed his focus to other amphipods {Onisimus normani) namely those associated with deep water (700m) cnidarians (Bolocera tuedeae) in Korsljorden south of Bergen. In the beginning he found almost two amphipods for every host, but after a few years they “disappeared”, and his PhD-studies came to a halt. During this time, Wim and his wife Sunniva had three children! They both eventually applied for jobs at the new University of Tromso (founded in 1968), and in 1973, Wim was offered the job as Zoological Conservator at the Tromso Museum. His responsibilities included “everything except insecta” - basically sponges to whales! After hearing something similar from someone in the US, Wim adopted his motto that “his science is like the Mississippi River: three miles wide and five inches deep.” While at the Tromso Museum, Wim believes he worked with every animal phylum. After colleague Einar Bruun died in an accident, for just over 10 years (1976-1990) Wim worked almost extensively on seabirds. Money for study of seabirds became available as well, in part to a Seabird-crisis (induced by a capelin crisis) and an offshore oil industry. Wim supervised several W/m and two of his now six students on their theses on birds. Wim quickly became known as the grandchildren; Sigurd and “bird-man” and birding has always been a great hobby for him. He has Arianne. 55 Amphipod newsletter 36 kept a “Blog”: “Birds and Seasons in Tromso” for the last 10 years. Wim takes several holidays (more and more frequent) to go birding “everywhere.” Wim’s interests in amphipods and their assoeiates has always been there, and he has eontinued this researeh during his sabbatieals (Bodega Bay 1979-80, Seripps (La Jolla) 1986, Sydney 1993, Cape Town 1999, Cork 2000). Wim’s researeh on sueh groups eontinues today. When and why did Wim start the Amphipod Newsletter? In 1970, with work being done on the Mediterranean book and with Sandro Ruffo in Verona, Wim sent out a questionnaire to eolleagues (ANl) asking if they wanted sueh a bibliography or any help? This was diseussed in Verona with Wim, Traudl Krapp-Sehiekel, Alan Myers, Gordan Karaman, Denise Bellan-Santini, Ulrieh Sehieeke and Sandro Ruffo. Sueh a positive response led to AN2 in 1972. Early ANs were mimeographs, and Wim relied upon regional helpers for assistanee mainly to solieit subseribers and to eolleet money. For some years they got some fmaneial support from Zootax (Sweden). Eventually AN was published eleetronieally. All remaining W/m and Riet - at the XIV ICA in Seville. subseription funding was used towards student travel stipends to attend meetings (Hungary /Tihany and Seville). Over the years, many people eontributed information and eitations to the AN’s partieularly Jan Stoek (Amsterdam), Juri Vinogradov (Moseow) and Franz Krapp (Bonn). Although the Tromso Museum gave Wim time to work on sueh projeets, namely the AN, many hours was done on his own time. Wim and his binoculars - ready to spot birds Verona-group: In 1967, Traudl Krapp-Sehiekel wrote to Wim asking about amphipods, and when Sandro Ruffo organized (1968) a meeting for writing the Monograph of Mediterranean Amphipods, Wim was ineluded. They had no eommon language for the whole group: they 56 considered French, but not all of them knew French; five in the group spoke Italian. So, part of the work was done in English, and it was decided early on that the monograph should be written in English - Sandro Ruffo knew no English. However Sandro coordinated and organized it all! Wim says his notes from these meetings were in a mixture of Dutch, French, English and probably something that looks almost like Italian (which he did not know). Wim was part of the 4th book/part of the Monograph - where he made an (illustrated) key to all families of amphipods in the Mediterranean. This is one of the things he still continues to make for several papers. He has continued to work with Traudl since these meetings with just last February visiting her in Adendorf for an unbelievable 26^^ time! Over the years they continue to keep a close and personal friendship. Amphipod Meetings - What is good (lovely!) with “the Amphipod family” is that there are no feuds. Most Amphipodologists seem to be personal friends, with amphipod meetings that are more a family gathering, and Wim feels (and hopes) that the new and “young” amphipod workers are included in this family feeling. No fights scientifically - this must have helped the progression of the amphipod work. The big “gurus” (J. Barnard, J. Stock, E. Bousfield, J. Eowry, etc) have always helped others - this is also very, very good! We have been lucky in this aspect! Wim says it’s very nice to see new “centres” of amphipod studies (Turkey, Iran, Tunisia, Brazil...) that have developed. The Polish group of amphipod workers particularly, have been important in keeping this good environment, and of course also Traudl. He has visited the homes of many amphipod workers (ex Traudl, Jim, Alan, Denise Bellan-Santini, Jerry Barnard, Geoff Moore, Ed Bousfield, Kathy Conlan and others) it shows the types of friendly relationships we have in our amphipod group/family. What is/are your favorite amphipod species name? (not an easy question to answer) the genus Hoho is good ;) likes names the stand out a little... (from Mollusca he really likes Abra cadabra...) What amphipod appendage (s) do you like illustrating the best? He does not like illustrating pieces - but pereopods are the easiest... Uropods are ok. What amphipod appendage (s) do you like illustrating the least? Mandibles, gnathopods often. Where is/are your favorite place (s) to collect amphipods? Bodega Bay (CA) and Falklands Islands were great places to sample - and intertidal on sandy beaches and sand fiats have been a favorite since childhood. (Wim has a friend who wrote a paper on “the beach when there is nothing to find there” and got inspired from this) Places you wished you never tried to collect amphipods? on the open sea on a small boat is not a favorite, (then you first fear you might die and then you fear you might not die) - but most all amphipod collecting trips have been great. Intertidal sampling on the beach at Bear Island in the Barents Sea was not the greatest amphipod moment. Describe/name your most memorable amphipod moment(s)? Sieving amphipods on the beaches and mudflats of Holland, and also searching for amphipods on the beaches of the Falkland Islands together with my daughter have been very happy moments. Finding associated amphipods on or in new hosts have also always given me a “kick”, for example on crabs at the Falklands, or on Pagurida in Australia.. (by Anne Helene and Adam) Wim field sampling with students Jon Roger and Cedric. 57 Amphipod newsletter 36 Dates and place for the 15th ICA already set up We are pleased to announce that the 15th International Colloquium on Amphipoda organized by the team from the Department of Invertebrate Zoology & Hydrobiology University of Lodz is hnally scheduled to take place from 2"'^ to 7* of September 20 1 3 in Szczawnica in Poland. Szczawnica is the pearl of the Polish health resorts. It is situated on the border of the Sqdeckie Beskids and the Pieniny Mountains in the picturesque valley of the rivulet Grajcarek. It is one of the most beautiful corners of Poland. The picturesque mountainous landscape with its unique gorge of the Dunajec, the vicinity of the Pieniny National Park and the Poprad Landscape Park make Szczawnica one of the most attractive tourist localities in Poland. To its geological foundations owes the health resort Szczawnica its mineral alkaline-salty waters, used in a variety of treatments. Concerning the transportation options, Szczawnica may be easily reached by bus from Krakow (Cracov), where the international Krakow Airport ( http:/ /www.krakowairport.pl/ en) is located. Alternatively, Szczawnica is easily reached by car through the A4 highway ( http:/ / en.wikipedia.org/ wiki/ A4 autostrada %28Poland%29) from Germany. The colloquium will be held in ‘JAN” HOTEL ( http:// www.hoteljan.net.pl/index en.php) . which is situated in a very peaceful and natural place, on the forest border, about 5 km from the city center, 1 00m from the main road. We will open the official 15* IGA website and Facebook page with preliminary schedule and pre-registration panel in September 2012. Following the long tradition of IGA we are trying to keep the costs at low limits, and due to the generally unstable economic situation in Europe we are not able to make the dehnite calculations such early. Thus, concerning the registration fee and accommodation prices, we will inform you about that in January 2013 at latest. We are looking forward to meet you all next year! On behalf of the organizing committee, Michal Grabowski Karolina Bacela-Spychalska More information upon the Szczawnica and its beautiful surroundings you may find under the following links: htto://en. wikiDedia.org/wiki/Szczawnica http://en. wikipedia.org/wiki/ Pieniny National Park %28Poland%29 http://en. wikipedia.org/wiki/ Dunaiec River Gorge http://en.wikipedia.org/wiki/Trzv Koronv http://www.pieninypn.pl/index.html7lang id=UK 58 Amphipod newsletter 36 New frontiers in Monitoring European Biodiversity: "The role and importance of Amphipod crustaceans" We walked through a pelting rain to reach the Botanical Garden of Palermo (Sicily, Italy) on the 27^^ of September 2011 for the MEB Conference, but when we reached the building and went through the door of the reception to start the usual queue for the registration, there were a lot of smiles around. There I had the conhrmation that I was missing that atmosphere. The idea of a big family is not trivial, I breathed the air of the Amphipod meetings from when I was a student and like what happens in big families the younger learns from the most expert and is grateful for this. The meeting in Palermo followed the same rule and was not different from the previous Amphipod meetings. And like the others it was a synergy of scientihc and human experiences. Traudl opened the Conference with her usual humor, introducing the importance of Amphipod taxonomy, and a total of 34 stimulating oral presentations followed on different topics: taxonomy and diversity of Amphipods, inspection of the modern tools based on morphological and molecular characters, the use of Amphipods in environmental monitoring and the impact of decline in traditional taxonomy on research. The oral presentations concluded with the instructive and amusing movie presented by Dirk on a male Amphipod guarding on a female. At the same time 34 posters were housed in the nearby historical building of Gymnasium within the Garden and scientihc discussions took place between a walk under the rich and exotic vegetation, a coffee and a stop in front of the posters. Some of the time for relax was dedicated to visit the historical Jails and the Ghiaramonte Palace now seat for the University of Palermo offices, and during the hnal dinner in the Gymnasium of the Botanical Garden on September the 29*, the participants could degust various Sicilian foods and wines, while local musicians played live folk music and the Sicilian Tarantella. This was the occasion for dancing, for laughing and for wishing to everybody all the best till the next meeting. A big thank to Sabrina Lo Brutto, to Valerio Ketmaier and to all their staff, and also to all the participant to the meeting for having made it so intense. Claudia Rossano For contributions to future Amphipod newsletters: Please contact Adam (abaldinger(at)oeb.harvardedu), Miranda (m.lowe(at)nhm.uk) or Anne Helene (annehelene.tandberg(at)imr.no). We are always happy to hear fromyou: what do you want us to include in the newsletter, do you have information about meetings, how do you think we can improve? Thankyou for your help! 59