Published March 4, 2021 | Version v1
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Jassa (Crustacea: Amphipoda): a new morphological and molecular assessment of the genus

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Conlan, Kathleen E., Desiderato, Andrea, Beermann, Jan (2021): Jassa (Crustacea: Amphipoda): a new morphological and molecular assessment of the genus. Zootaxa 4939 (1): 1-191, DOI: 10.11646/zootaxa.4939.1.1

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  • Adami, M.L. & Gordillo, S. (1999) Structure and dynamics of the biota associated with Macrocystis pyrifera (Phaeophyta) from the Beagle Channel, Tierra del Fuego. Scientia Marina, 63 (Supplement 1), 183-191. https://doi.org/10.3989/scimar.1999.63s1183
  • Almeida, L.P. & Coolen, J.W.P. (2020) Modelling thickness variations of macrofouling communities on offshore platforms in the Dutch North Sea. Journal of Sea Research, 56, 101836. https://doi.org/10.1016/j.seares.2019.101836
  • Alonso de Pina, G.M. (2005) Anew species of Notopoma Lowry & Barents, 1996, and a new record of Jassa marmorata Holmes, 1905, from the southwestern Atlantic (Amphipoda: Corophiidea: Ischyroceridae). Proceedings of the Biological Society of Washington, 118, 528-538. https://doi.org/10.2988/0006-324X(2005)118[528:ANSONL]2.0.CO;2
  • Angelone, M., Gasparini, C., Guerra, M., Lombardi, S., Pizzino, L., Quattrocchi, F., Sacchi, E. & Zuppi, G.M. (2005) Fluid geochemistry of the Sardinian Rift-Campidano Graben (Sardinia, Italy): fault segmentation, seismic quiescence of geochemically "active" faults, and new constraints forselection of CO2 storage sites. Applied Geochemistry, 20 (2), 317-340. https://doi.org/10.1016/j.apgeochem.2004.08.008
  • Armsby, M. & Tisch, N. (2006) Intraguild predation and cannibalism in a size-structured community of marine amphipods. Journal of Experimental Marine Biology and Ecology, 333, 286-295. https://doi.org/10.1016/j.jembe.2006.01.004
  • Barnard, J.L. (1969) Gammaridean amphipoda of the rocky intertidal of California: Monterey Bay to La Jolla. Bulletin of the United States National Museum, 258, 1-230. https://doi.org/10.5479/si.03629236.258.1
  • Barnard, J.L. (1974) Gammaridean Amphipoda of Australia, Part II. Smithsonian Institution Press, Washington. 148 pp. https://doi.org/10.5479/si.00810282.139
  • Barnard, J.L. & Karaman, G.S. (1991) The families and genera of marine gammaridean Amphipoda (except marine gammaroids) (Part 1). Records of the Australian Museum, Supplement 13, 419-866. https://doi.org/10.3853/j.0812-7387.13.1991.367
  • Barnard, J.L. & Reish, D.J. (1959) Ecology of Amphipoda and Polychaeta of Newport Bay, California. Allan Hancock Foundation Publications, Occasional Paper, 21, 1-106.
  • Barnes, D.K.A., Griffiths, H.J. & Kaiser, S. (2009) Geographic range shift responses to climate change by Antarctic benthos: where we should look. Marine Ecology Progress Series, 393, 13-26. https://doi.org/10.3354/meps08246
  • Bate, C.S. (1862) Catalogue of the specimens of amphipodous Crustacea in the collection of the British Museum. Taylor & Francis, London, 399 pp.
  • Bate, C.S. & Westwood, J.O. (1863) Ahistory of the British sessile-eyed Crustacea. Vol. I. John van Voorst, London, 507 pp. https://doi.org/10.5962/bhl.title.9917
  • Bate, C.S. & Westwood, J.O. (1868) Ahistory of the British sessile-eyed Crustacea. Vol. II. John van Voorst, London. 536 pp.
  • Beermann, J. (2014) Spatial and seasonal population dynamics of sympatric Jassa species (Crustacea, Amphipoda). Journal of Experimental Marine Biology and Ecology, 459, 8-16. https://doi.org/10.1016/j.jembe.2014.05.008
  • Beermann, J. & Boos, K. (2015) Flexible microhabitat partitioning between hemi-sessile congeners. Marine Ecology Progress Series, 520, 143-151. https://doi.org/10.3354/meps11115
  • Beermann, J. & Franke, H.-D. (2011) Asupplement to the amphipod (Crustacea) species inventory of Helgoland (German Bight, North Sea): indication of rapid recent change. Marine Biodiversity Records, 4, e41. https://doi.org/10.1017/S1755267211000388
  • Beermann, J. & Franke, H.-D. (2012) Differences in resource utilization and behaviour between coexisting Jassa species (Crustacea, Amphipoda). Marine Biology, 159 (5), 951-957. https://doi.org/10.1007/s00227-011-1872-7
  • Beermann, J., Hall-Mullen, A.K., Havermans, C., Coolen, J.W.P., Crooijmans, R.P.M.A., Dibbits, B., Held, C. & Desiderato, A. (2020) Ancient globetrotters-connectivity and putative native ranges of two cosmopolitan biofouling amphipods. PeerJ, 8, e9613. https://doi.org/10.7717/peerj.9613
  • Beermann, J. & Purz, A.K. (2013) Comparison of life history parameters in coexisting species of the genus J assa (Amphipoda, Ischyroceridae). Journal of Crustacean Biology, 33 (6), 784-792. https://doi.org/10.1163/1937240X-00002190
  • Bellan, G. (1980) Relationship of pollution to rocky substratum polychaetes on the French Mediterranean coast. Marine Pollution Bulletin, 11 (11), 318-321. https://doi.org/10.1016/0025-326X(80)90048-X
  • Bennett, B. Griffiths, C.L. & Penrith, M.-L. (1983) The diets of littoral fish from the Cape Peninsula. South African Journal of Zoology, 18 (4), 343-352. https://doi.org/10.1080/02541858.1983.11447837
  • Blankley, W.O. (1982) Feeding ecology of three inshore fish species at Marion Island (Southern Ocean). South African Journal of Zoology, 17 (4), 164-170. https://doi.org/10.1080/02541858.1982.11447798
  • Bloecher, N., Olsen, Y. & Guenther, J. (2013) Variability of biofouling communities on fish cage nets: A 1-year field study at a Norwegian salmon farm. Aquaculture, 416-417, 302-309. https://doi.org/10.1016/j.aquaculture.2013.09.025
  • Boeck A. (1871) Bidrag til Californiens amphipodefauna. Forhandlinger i Videnskabs-Selskabet i Christiana, 1871, 32-51.
  • Bonifazi, A., Lezzi, M., Ventura, D., Lisco, S., Cardone, F. & Gravina, M.F. (2019) Macrofaunal biodiversity associated with different developmental phases of a threatened Mediterranean Sabellaria alveolata (Linnaeus, 1767) reef. Marine Environmental Research, 145, 97-111. https://doi.org/10.1016/j.marenvres.2019.02.009
  • Bonifazi, A., Mancini, E. & Ventura, D. (2018) First record of the invasive and cryptogenic species Jassa slatteryi Conlan, 1990 (Crustacea: Amphipoda) in Italian coastal waters. Journal of Sea Research, 136, 37-41. https://doi.org/10.1016/j.seares.2018.03.005
  • Borowsky, B. (1983) Reproductive behavior of three tube-building peracarid crustaceans: the amphipods Jassa falcata and Ampithoe valida and the tanaid Tanais cavolinii. Marine Biology, 77, 257-263. https://doi.org/10.1007/BF00395814
  • Borowsky, B. (1985) Differences in reproductive behavior between two male morphs of the amphipod crustacean Jassa falcata Montagu. Physiological Zoology, 58 (5), 497-502. https://doi.org/10.1086/physzool.58.5.30158577
  • Bouckaert, R.R. & Drummond,A.J. (2017) ModelTest: Bayesianphylogeneticsite modelaveragingandmodel comparison. BMC Evolutionary Biology, 17 (1), 42. https://doi.org/10.1186/s12862-017-0890-6
  • Bousfield, E.L. (1952) Zoological investigations in the Maritime provinces. Annual report of the National Museum of Canada 1950-1951. Bulletin of the National Museum of Canada, 126, 188-194.
  • Bousfield, E.L. (1956a) Malacostracan crustaceans from the shores of western Nova Scotia. Proceedings of the Nova Scotian Institute of Science, 24, 1954-1958.
  • Bousfield, E.L. (1956b) Studies on the shore Crustacea collected in eastern Nova Scotia and Newfoundland, 1954. Bulletin of the National Museum of Canada, 142, 127-152.
  • Bousfield, E.L. (1958) Littoral marine arthropods and mollusks collected in western Nova Scotia, 1956. Proceedings of the Nova Scotia Institute of Science, 1956-1957, 24, 303-325.
  • Bousfield, E.L. (1962) Studies on littoral marine arthropods from the Bay of Fundy region. Bulletin of the National Museum of Canada, 183, 42-62.
  • Bousfield, E.L. (1973) Shallow-water Gammaridean Amphipoda of New England. Cornell University Press, Ithaca, New York, 324 pp.
  • Bousfield, E.L. & Laubitz, D.R. (1972) Station lists and new distributional records of littoral marine invertebrates of the Canadian Atlantic and New England region. National Museums of Canada, Publications in Biological Oceanography, 5, 1-49.
  • Bousfield, E.L. & Leim, A.H. (1959) The fauna of Minas Basin and Minas Channel. Bulletin of the National Museum of Canada, 166, 1-30.
  • Brawley, S.H. & Fei, X.G. (1987) Studies of mesoherbivory in aquaria and in an unbarricaded mariculture farm on the Chinese coast. Journal of Phycology, 23, 614-623. https://doi.org/10.1111/j.1529-8817.1987.tb04214.x
  • Bueno, M. & Leite, F.P.P. (2019) Age and life style affect macroalgae colonization by amphipods in shallow marine environments. Journal of Experimental Marine Biology and Ecology, 514, 59-66. https://doi.org/10.1016/j.jembe.2019.03.013
  • Bunker, F. (2004) Biology and Video Surveys of North Hoyle Wind Turbines, 11-13 August 2004. Report to Centre for Marine and Coastal Studies Ltd (CMACS) by MarineSeen, Estuary Cottage, Bentlass, Hundleton, Pembrokeshire SA71 5RN. MarineSeen, Estuary Collage, Bentlass, Bentlass, Hundleton, Pembrokeshire, 32 pp.
  • Caplins, S.A. & Turbeville, J.M. (2011) Feeding rates of the nemertean Prosorhochmus americanus (Hoplonemertea) on two species of gammaridean amphipods. Invertebrate Biology, 130 (1), 34-42. https://doi.org/10.1111/j.1744-7410.2010.00211.x
  • Carlton, J.T., Chapman, J.W., Geller, J.B., Miller, J.A., Carlton, D.A., McCuller, M., Treneman, N.C., Steves, B.P. & Ruiz, G.M. (2017) Tsunami-driven rafting: Transoceanic species dispersal and implications for marine biogeography. Science, 357 (6358), 1402-1406. https://doi.org/10.1126/science.aao1498
  • Carlton, J.T., Chapman, J.W., Geller, J.B., Miller, J.A., Carlton, D.A., McCuller, M., Treneman, N.C., Steves, B.P. & Ruiz, G.M. (2019) Chapter 7: Characterization of the invertebrate, protist, and fish biodiversity arriving with Japanese tsunami marine debris in North America and the Hawaiian Islands. In: Clarke Murray, C., Therriault, T.W., Maki, H. & Wallace, N. (Eds.), The Effects of Marine Debris Caused by the Great Japan Tsunami of 2011. PICES Special Publication 6. North Pacific Marine Science Organization (PICES), Sidney, British Columbia, pp. 69-99. Available from: https://core.ac.uk/download/ pdf/286777757.pdf (accessed 20 January 2021)
  • Carlton, J.T. & Hodder, J. (1995) Biogeography and dispersal of coastal marine organisms: experimental studies on a replica of a 16th-century sailing vessel. Marine Biology, 121 (4), 721-730. https://doi.org/10.1007/BF00349308
  • Cartes, J.E. & Sorbe, J.C. (1999) Deep-water amphipods from the Catalan Sea slope (western Mediterranean): Bathymetric distribution, assemblage composition and biological characteristics. Journal of Natural History, 33 (8), 1133-1158. https://doi.org/10.1080/002229399299978
  • Chan, F.T., MacIsaac, H.J. & Bailey, S.A. (2015) Relative importance of vessel hull fouling and ballast water as transport vectors of nonindigenous species to the Canadian Arctic. Canadian Journal of Fisheries and Aquatic Sciences, 72 (8), 1230-1242. https://doi.org/10.1139/cjfas-2014-0473
  • Chilton, C. (1883) Further additions to our knowledge of the New Zealand Crustacea. Transactions and Proceedings of the New Zealand Institute, 15, 69-86.
  • Chilton, C. (1884) Additions to the sessile-eyed Crustacea of New Zealand. Transactions and Proceedings of the New Zealand Institute, 16, 249-265.
  • Chilton C. (1911) Note on the dispersal of marine Crustacea by means of ships. Transactions and Proceedings of the New Zealand Institute, 43, 131-133.
  • Choi, H.C., Huh, S.-J. & Park, J.M. (2017) Size-related and temporal dietary variations of Hexagrammos otakii in the mid-western coast of Korea. Korean Journal of Ichthyology, 29 (2), 117-123.
  • Clancy, N. (1997) Environmental and population-specific contributions to growth rate variation in the marine amphipod Jassa marmorata Holmes. Journal of Experimental Marine Biology and Ecology, 209, 185-200. https://doi.org/10.1016/S0022-0981(96)02683-4
  • Clark, R.A. (1997) Dimorphic males display alternative reproductive strategies in the marine amphipod Jassa marmorata Holmes (Corophioidea: Ischyroceridae). Ethology, 103, 531-553. https://doi.org/10.1111/j.1439-0310.1997.tb00166.x
  • Clark, R. & Caudill, C.C. (2001) Females of the marine amphipod Jassa marmorata mate multiple times with the same or different males. Marine and Freshwater Behaviour and Physiology, 34, 131-138. https://doi.org/10.1080/10236240109379066
  • Clarke Murray, C., Carlton, J.T., Nelson, J.C., Ruiz, G.M. & Therriault, T.W. (2019) Chapter 16: An evaluation of Japanese Tsunami Marine Debris as a potential vector of invasive species. In: Clarke Murray, C., Therriault, T.W., Maki, H. & Wallace, N. (Eds.), The Effects of Marine Debris Caused by the Great Japan Tsunami of 2011. PICES Special Publication 6. North Pacific Marine Science Organization (PICES), Sidney, British Columbia, pp. 243-259. Available from: https://core. ac.uk/download/pdf/286777757.pdf (accessed 20 January 2021)
  • Coleman, C.O. (1994) Karyological studies in Amphipoda (Crustacea). Ophelia 39 (2), 93-105. https://doi.org/10.1080/00785326.1994.10429537
  • Conlan, K.E. (1989) Delayed reproduction andadult dimorphism in malesof theamphipod genus Jassa (Corophioidea: Ischyroceridae): an explanation for systematic confusion. Journal of Crustacean Biology, 9 (4), 601-625. https://doi.org/10.1163/193724089X00629
  • Conlan, K.E. (1990) Revision of the crustacean amphipod genus Jassa Leach (Corophioidea: Ischyroceridae). Canadian Journal of Zoology, 68, 2031-2075. https://doi.org/10.1139/z90-288
  • Conlan, K.E. (1995) Thumbing doesn't always make the genus: revision of Microjassa Stebbing (Crustacea: Amphipoda: Ischyroceridae). Bulletin of Marine Science, 57, 333-377. https://doi.org/10.1139/z90-288
  • Conlan, K.E. (2021) New genera for species of Jassa Leach (Crustacea: Amphipoda) and their relationship to a revised Ischyrocerini. Zootaxa, 4921 (1), 001-072. https://doi.org/10.11646/zootaxa.4921.1.1
  • Conradi, M. & Lopez-Gonzalez, P.J. (1999) The benthic Gammaridea (Crustacea, Amphipoda) fauna of Algeciras Bay (Strait of Gibraltar): distributional ecology and some biogeographical considerations. Helgoland Marine Research, 53 (1), 2-8. https://doi.org/10.1007/PL00012134
  • Conradi, M., Lopez-Gonzalez, P.J., Cervera, J.L. & Garcia-Gomez, C. (2000) Seasonality and spatial distribution of peracarids associated with the bryozoan Bugula neritina in Algeciras Bay, Spain. Journal of Crustacean Biology, 20 (2), 334-349. https://doi.org/10.1163/20021975-99990045
  • Coolen, J.W., Lengkeek, W., van der Have, T. & Bittner, O. (2019) Upscaling positive effects of scour protection in offshore wind farms: Quick scan of the potential to upscale positive effects of scour protection on benthic macrofauna and associated fish species. Wageningen Marine Research Report C008/19. Wageningen Marine Research, Den Helder, 34 pp. https://doi.org/10.18174/475354
  • Coolen, J.W., Van Der Weide, B., Cuperus, J., Blomberg, M., Van Moorsel, G.W., Faasse, M.A., Bos, O.G., Degraer, S. & Lindeboom, H.J. (2018) Benthic biodiversity on old platforms, young wind farms, and rocky reefs. ICES Journal of Marine Science, 77 (3), 1250-1265. https://doi.org/10.1093/icesjms/fsy092
  • Copilas-Ciocianu, D., Sidorov, D. & Gontcharov, A. (2019) Adrift across tectonic plates: molecular phylogenetics supports the ancient Laurasian origin of old limnic crangonyctid amphipods. Organisms Diversity & Evolution, 19 (2), 191-207. https://doi.org/10.1007/s13127-019-00401-7
  • Costa, M.F.B., Mansur, K.F.R. & Leite, F.P.P. (2015) Temporal variation of the gammaridean fauna (Crustacea, Amphipoda) associated with the sponge Mycale angulosa (Porifera, Demospongiae) in southeastern Brazil. Nauplius, 23 (1), 79-87. https://doi.org/10.1590/S0104-64972015002312
  • Craig M.T., Burke, J., Clifford, K., Mochon-Collura, E., Chapman, J.W. & Hyde, J.R. (2018) Trans-Pacific rafting in tsunami associated debris by the Japanese yellowtail jack, Seriola aureovittata Temminck & Schlegel, 1845 (Pisces, Carangidae). Aquatic Invasions, 13 (1), 173-177. https://doi.org/10.3391/ai.2018.13.1.13
  • Dailey, M.D., Gulland, F.M., Lowenstine, L.J., Silvagni, P. & Howard, D. (2000) Prey, parasites and pathology associated with the mortality of a juvenile gray whale (Eschrichtius robustus) stranded along the northern California coast. Diseases of Aquatic Organisms, 42 (2), 111-117. https://doi.org/10.3354/dao042111
  • Dana, J.D. (1852a) Conspectus crustaceorum quae in orbis terrarum circumnavigatione, Carolo Wilkes e classe Reipublicae Faederatae Duce, lexit et descripsit Jacobus D. Dana, Pars III (Amphipoda n°1). Proceedings of the American Academy of Arts and Sciences, 2, 201-220.
  • Dana, J.D. (1852b) On the classification of the Crustacea Choristopoda or Tetradecapoda. American Journal of Sciences and Arts, Series 2, 14, 297-316.
  • Dana, J.D. (1853) Crustacea. Part II. United States Exploring Expedition, during the years 1838, 1839, 1840, 1841, 1842, under the command of Charles Wilkes. U.S.N.C., 14, 689-1618.
  • Dauvin, J.C., Andrade, H., de-la-Ossa-Carretero, J.A., Del-Pilar-Ruso, Y. & Riera, R. (2016) Polychaete/amphipod ratios: An approach to validating simple benthic indicators. Ecological Indicators, 63, 89-99. https://doi.org/10.1016/j.ecolind.2015.11.055
  • Dauvin, J.C., Pezy, J.P., Baffreau, A., Bachelet, Q., Baux, N., Mear, Y., Murat, A. & Poizot, E. (2020) Effects of a salmon fish farm on benthic habitats in a high-energy hydrodynamic system: The case of the Rade de Cherbourg (English Channel). Aquaculture, 518, 734832. https://doi.org/10.1016/j.aquaculture.2019.734832
  • Dauvin, J.C. & Ruellet, T. (2007) Polychaete/amphipod ratio revisited. Marine Pollution Bulletin, 55 (1-6), 215-224. https://doi.org/10.1016/j.marpolbul.2006.08.045
  • Davoult, D., Surget, G., Stiger-Pouvreau, V., Noisette, F., Riera, P., Stagnol, D., Androuin, T. & Poupart, N. (2017) Multiple effects of a Gracilaria vermiculophylla invasion on estuarine mudflat functioning and diversity. Marine Environmental Research, 131, 227-235. https://doi.org/10.1016/j.marenvres.2017.09.020
  • de-la-Ossa-Carreterro, A. & Dauvin, J.C. (2010) Acomparison of two biotic indices, AMBI and BOPA/BO2A, for assessing the ecological quality status (EcoQS) of benthic macro-invertebrates. Transitional Waters Bulletin, 4 (1), 12-24. https://doi.org/10.1285/i1825229Xv4n1p12
  • Della Valle, A. (1893) Fauna und flora des Golfes von Neapel und der angrenzenden meeres-abschnitte herausgeben von der zoologischen station zu Neapel. 20. Monographie: Gammarini. R. Friedlander & Sohn, Berlin, 948 pp.
  • De Troch, M., Reubens, J.T., Heirman, E., Degraer, S. & Vincx, M. (2013) Energy profiling of demersal fish: Acase-study in wind farm artificial reefs. Marine Environmental Research, 92, 224-233. https://doi.org/10.1016/j.marenvres.2013.10.001
  • Dennenmoser, S. & Thiel, M. (2015) Cryptic female choice in crustaceans. In: Peretti, A.V. & Aisenberg, A. (Eds.), Cryptic Female Choice in Arthropods. Patterns, Mechanisms and Prospects. Springer International Publishing, Cham, pp. 203-237. https://doi.org/10.1007/978-3-319-17894-3_8
  • Derweduwen, R.J., Wittoeck, J. & Hostens, K. (2016) Chapter 10. Feeding behaviour of Lesser Weever (Echiichthys vipera) and Dab (Limanda limanda) in the C-Power Wind farm. In: Environmental impacts of offshore wind farms in the Belgian part of the North Sea: Environmental impact monitoring reloaded. Marine Ecology and Management Section, OD Natural Environment, Royal Belgian Institute of Natural Sciences, Brussels, pp. 143-166.
  • Desiderato, A. (2020) Amphipod fouling: diversity, biogeography and drivers of an understudied community. Ph.D. Thesis, Universidade Federal do Parana, Curitiba, 198 pp.
  • Deysher, L.E. (1984) Reproductive phenology of newly introduced populations of the brown alga Sargassum muticum (Yendo) Fensholt. Hydrobiologia, 116/117, 403-407. https://doi.org/10.1007/BF00027710
  • Di Camillo, C.G., Giordano, G., Bo, M., Betti, F., Mori, M., Puce, S. & Bavestrello, G. (2013) Seasonal patterns in the abundance of Ectopleura crocea (Cnidaria: Hydrozoa) on a shipwreck in the Northern Adriatic. Marine Ecology, 34, 25-32. https://doi.org/10.1111/maec.12025
  • Diviacco, G. (1979) Icrostacei anfipodi del fouling nella centrale termoelettrica di Vado Ligure (Savona). Bolletino dei Musei e degli Istituti Biologici dell' Universita di Genova, 47, 93-99.
  • Dixon, I.M.T. & Moore, P.G. (1997) Acomparative study on the tubes and feeding behaviour of eight species of corophioid Amphipoda and their bearing on phylogenetic relationships within the Corophioidea. Philosophical Transactions of the Royal Society of London B, 352, 93-112. https://doi.org/10.1098/rstb.1997.0006
  • Domenech, F., Badillo, F.J., Tomas, J., Raga, J.A. & Aznar, F.J. (2015) Epibiont communities of loggerhead marine turtles (Caretta caretta) in the western Mediterranean: influence of geographic and ecological factors. Journal of the Marine Biological Association of the United Kingdom, 94 (4), 851-861. https://doi.org/10.1017/S0025315414001520
  • Donahue, M.J., Nichols, A., Santamaria, C.A., League-Pike, P.E., Krediet, C.J., Perez, K.O. & Shulman, M.J. (2009) Predation risk, prey abundance, and the vertical distribution of three brachyuran crabs on Gulf Of Maine Shores. Journal of Crustacean Biology, 29 (4), 523-531. https://doi.org/10.1651/08-3061.1
  • Drummond, A.J. & Bouckaert, R.R. (2014) Bayesian Evolutionary Analysis with BEAST 2. Cambridge University Press. 249 pp. https://doi.org/10.1017/CBO9781139095112
  • Duchene, J.C. (2012) Hydroid and serpulid recruitment patterns using a new laser microtopography technique. Journal of Experimental Marine Biology and Ecology, 412, 27-36. https://doi.org/10.1016/j.jembe.2011.10.016
  • d'Udekem d'Acoz, C. (1993) Presence et abondance de Jassa herdmanni (Walker, 1893) sur la cote belge (Crustacea, Amphipoda, Ischyroceridae). De Strandvlo, 13 (4), 134-138.
  • d'Udekem d'Acoz, C. (2010) Contribution to the knowledge of European Liljeborgiidae (Crustacea, Amphipoda), with considerations on the family and its affinities. Bulletin of the Royal Belgian Institute of Natural Sciences, Biology, 80, 127-259.
  • Duffy, J.E. (1990) Amphipods on seaweeds: partners or pests? Oecologia, 83, 267-276. https://doi.org/10.1007/BF00317764
  • Eilertsen, M., Norderhaug, K.M. & Sjotun, K. (2011) Does the amphipod fauna associated with epiphytes on kelp (Laminaria hyperborea) change with depth? Marine Biology Research, 7, 224-234. https://doi.org/10.1080/17451000.2010.492592
  • Ellis, D. & Stoker, M.S. (2014) The Faroe-Shetland Basin: a regional perspective from the Paleocene to the present day and its relationship to the opening of the North Atlantic Ocean. Geological Society, London, Special Publications, 397 (1), 11-31. https://doi.org/10.1144/SP397.1
  • Farris, D.W., Jaramillo, C., Bayona, G., Restrepo-Moreno, S.A., Montes, C., Cardona, A., Mora, A., Speakman, R.J., Glascock, M.D. & Valencia, V. (2011) Fracturing of the Panamanian Isthmus during initial collision with South America. Geology, 39 (11), 1007-1010. https://doi.org/10.1130/G32237.1
  • Fernandez-Gonzalez, V., Fernandez-Jover, D., Toledo-Guedes, K. & Valero-Rodriguez, J.M. (2014) Nocturnal planktonic assemblages of amphipods vary due to the presence of coastal aquaculture cages. Marine Environmental Research, 101, 22-28. https://doi.org/10.1016/j.marenvres.2014.08.001
  • Fernandez-Gonzalez, V., Martinez-Garcia, E. & Sanchez-Jerez, P. (2016) Role of fish farm fouling in recolonisation of nearby soft-bottom habitats affected by coastal aquaculture. Journal of Experimental Marine Biology and Ecology, 474, 210- 215. https://doi.org/10.1016/j.jembe.2015.10.019
  • Fernandez-Gonzalez, V. & Sanchez-Jerez, P. (2017) Fouling assemblages associated with off-coast aquaculture facilities: an overall assessmentof the Mediterranean Sea. Mediterranean Marine Science, 18, 87-96. https://doi.org/10.12681/mms.1806
  • Fernandez-Leborans, G., Fernandez-Gonzalez, V., Sanchez-Jerez, P. & Roura, A. (2016) Epibiontic associations between apostomid ciliates Conidophrys spp. and amphipods associated with fish farms fouling in the western Mediterranean Sea. Helgoland Marine Research, 7, 1-12. https://doi.org/10.1186/s10152-016-0463-x
  • Fitzpatrick, J.F. (1987) Notes on the so-called "blue color phase" in North American cambarid crawfishes (Decapoda, Astacoidea). Crustaceana, 52 (3), 316-319. https://doi.org/10.1163/156854087X00556
  • Flynn, M.N. & Valerio-Berardo, M.T. (2009) Depth-associated patterns in the development of Amphipoda (Crustacea) assemblages on artificial substrata in the S"o Sebasti"o Channel, Southeastern Brazil. Nauplius, 17 (2), 127-134.
  • Flynn, M.N., Valerio-Berardo, M.T. & Pereira, W.R. (2011) Impacto ecotoxicologico do derramamento de petroleo, em S"o Sebastiao, Sao Paulo sobre as taxas vitais de populacao do anfipode Jassa slaterryi. Revista Intertox de Toxicologia, Risco Ambiental e Sociedade, 4 (3), 65-78. https://doi.org/10.22280/revintervol4ed3.95
  • Fofonoff, P.W., Ruiz, G.M., Steves, B., Simkanin, C. & Carlton, J.T. (2019) National exotic marine and estuarine species information system. Marine Invasions Lab, Smithsonian Environmental Research Center, Edgewater, Maryland.Available from: http://invasions.si.edu/nemesis/ (accessed 4 October 2019)
  • Folmer, O., Black, M., Hoeh, W., Lutz, R. & Vrijenhoek, R. (1994) DNA primers for amplification of mitochondrial cytochrome c oxidase subunit Ifrom diverse metazoan invertebrates. Molecular Marine Biology and Biotechnology, 3, 294-299.
  • Franz, D.R. (1989) Population density and demography of a fouling community amphipod. Journal of Experimental Marine Biology and Ecology, 125, 117-136. https://doi.org/10.1016/0022-0981(89)90038-5
  • Franz, D.R. & Mohamed, Y. (1989) Short-distance dispersal in a fouling community amphipod crustacean, Jassa marmorata Holmes. Journal of Experimental Marine Biology and Ecology, 133, 1-13. https://doi.org/10.1016/0022-0981(89)90154-8
  • Galil, B.S., Boero, F., Fraschetti, S., Piraino, S., Campbell, M.L., Hewitt, C.L., Carlton, J.T., Cook, E.J., Jelmert, A., Macpherson, E., Marchini, A., Occhipinti-Ambrogi, A., McKenzie, C.H., Minchin, D., Ojaveer, H., Olenin, S. & Ruiz, G. (2015) The enlargement of the Suez Canal and introduction of non-indigenous species to the Mediterranean Sea. Limnology and Oceanography Bulletin, 24 (2), 43-45. https://doi.org/10.1002/lob.10036
  • Genzano, G.N. (2005) Trophic ecology of a benthic intertidal hydroid, Tubularia crocea, at Mar del Plata, Argentina. Journal of the Marine Biological Association of the United Kingdom, 85 (2), 307-312. https://doi.org/10.1017/S0025315405011197h
  • Gittenberger, A., Rensing, M., Stegenga, H. & Hoeksema, B. (2010) Native and non-native species of hard substrata in the Dutch Wadden Sea. Nederlandse Faunistische Mededelingen, 33, 21-76.
  • Glarou, M., Zrust, M. & Svendsen J.C. (2020) Using artificial-reef knowledge to enhance the ecological function of offshore wind turbine foundations: implications for fish abundance and diversity. Journal of Marine Science and Engineering, 8 (332), 1-26. https://doi.org/10.3390/jmse8050332
  • Gonzalez, M.L., Perez-Schultheiss, J. & Lopez, D.A. (2011) Exotic amphipods in aquaculture systems: presence and potential use. Crustaceana, 84 (7), 769-775. https://doi.org/10.1163/001121611X579132
  • Gonzalez-Silvera, D., Izquierdo-Gomez, D., Fernandez-Gonzalez, V., Martinez-Lopez, F.J., Lopez-Jimenez, J.A. & Sanchez- Jerez, P. (2015) Mediterranean fouling communities assimilate the organic matter derived from coastal fish farms as a new trophic resource. Marine Pollution Bulletin, 91, 45-53 https://doi.org/10.1016/j.marpolbul.2014.12.029
  • Gouillieux, B. (2017) New records of benthic amphipods, Jassa slatteryi Conlan, 1990 and Ampithoe valida Smith, 1873 (Crustacea : Peracarida : Amphipoda) forthe Bayof Biscay, France, withmorphological notes. Cahiersde Biologie Marine, 58, 279-289. https://doi.org/10.21411/CBM.A.F205EFDE.
  • Gray, J.S., Clarke, K.R., Warwick, R.M. & Hobbs, G. (1990) Detection of initial effects of pollution on marine benthos: an example from the Ekofisk and Eldfisk oilfields, North Sea. Marine Ecology Progress Series, 66, 285-299. https://doi.org/10.3354/meps066285
  • Griffiths, C., Robinson, T. & Mead, A. (2011) The alien and cryptogenic marine crustaceans of South Africa. In: Galil, B.S., Clark, P.F. & Carlton, J.T. (Eds.), In the Wrong Place-Alien Marine Crustaceans: Distribution, Biology and Impacts. Invading Nature-Springer Series in Invasion Ecology. Vol. 6. Springer, Dordrect, pp. 269-282. https://doi.org/10.1007/978-94-007-0591-3_8
  • Guerra-Garcia, J.M., Ros, M., Izquierdo, D. & Soler-Hurtado, M. (2012) The invasive Asparagopsis armata versus the native Corallina elongata: Differences in associated peracarid assemblages. Journal of Experimental Marine Biology and Ecology, 416-417, 121-128. https://doi.org/10.1016/j.jembe.2012.02.018
  • Guerra-Garcia, J.M., Ruiz-Tabares, A., Baeza-Rojano, E., Cabezas, M.P., Diaz-Pavon, J.J., Pacios, I., Maestre, M., Gonzalez, A.R., Espinosa, F. & Garcia-Gomez, J.C. (2010) Trace metals in Caprella (Crustacea: Amphipoda). Anew tool for monitoring pollution in coastal areas? Ecological Indicators, 10 (3), 734-743. https://doi.org/10.1016/j.ecolind.2009.12.003
  • Guindon, S., Dufayard, J.F., Lefort, V., Anisimova, M., Hordijk, W. & Gascuel, O. (2010) New algorithms and methods to estimate maximum-likelihood phylogenies: Assessing the performance of PhyML 3.0. Systematic Biology, 59 (3), 307-321. https://doi.org/10.1093/sysbio/syq010
  • Gutow, L., Beermann, J., Buschbaum, C., Rivadeneira, M.M. & Thiel, M. (2015) Castaways can't be choosers-Homogenization of rafting assemblages on floating seaweeds. Journal of Sea Research, 95, 161-171. https://doi.org/10.1016/j.seares.2014.07.005
  • Haberlin, M.D. (2018) The role of fronts, eddies and bubbles on the distribution, abundance and advection of gelatinous zooplankton: new insights for finfish aquaculture. Ph.D. Thesis, University College Cork, Cork, 228 pp. http://creativecommons.org/licenses/by-nc-nd/3.0/
  • Hacker, S.D. & Steneck, R.S. (1990) Habitat architecture and the abundance and body-size-dependent habitat selection of a phytal amphipod. Ecology, 71 (6), 2269-2285. https://doi.org/10.2307/1938638
  • Hamdy, R., Langeneck, J., Atta, M.M., Dorgham, M.M., El-Rashidy, H.H. & Musco, L. (2019) Diversity and ecology of crustaceans from shallow rocky habitats along the Mediterranean coast of Egypt. Marine Biodiversity, 49 (1), 221-233. https://doi.org/10.1007/s12526-017-0787-z
  • Haska, C.L., Yarish, C., Kraemer, G., Blaschik, N., Whitlatch, R., Zhang, H. & Lin, S. (2012) Bait worm packaging as a potential vector of invasive species. Biological Invasions, 14, 481-493. https://doi.org/10.1007/s10530-011-0091-y
  • Haswell, W.A. (1879) On some additional new genera and species of amphipodous crustaceans. Proceedings of the Linnean Society of New South Wales, 4, 319-356. https://doi.org/10.5962/bhl.part.22854
  • Haswell, W.A., 1880. Preliminary report on the Australian Amphipoda. Annals and Magazine of Natural History, Series 5, 5, 30-34. https://doi.org/10.1080/00222938009459377
  • Haupt, T.M., Griffiths, C.L. & Robinson, T.B. (2012) Intra-regional translocations of epifaunal and infaunal species associated with cultured Pacific oysters Crassostrea gigas. African Journal of Marine Science, 34 (2), 187-194. https://doi.org/10.2989/1814232X.2012.673293
  • Havermans, C., De Broyer, C., Mallefet, J. & Zintzen, V. (2007) Dispersal mechanisms in amphipods: a case study of Jassa herdmani (Crustacea, Amphipoda) in the North Sea. Marine Biology, 153 (1), 83-89. https://doi.org/10.1007/s00227-007-0788-8
  • Heller, C. (1866) Beitrage zur naheren kenntnis der amphipoden des Adriatischen Meeres. Denkschriften. Akademie der Wissenschaften in Wien, Mathematisch-Naturwissenschaftliche Klasse, 26 (2), 1-62.
  • Hinojosa-Arango, G., Maggs, C.A., Johnson, M.P. & Riosmena-Rodriguez, R.R. (2013) When rhodoliths do not roll: Invertebrate community responses to environmental stability and natural disturbance. In: Riosmena-Rodriguez, R.R. (Ed.), Invertebrates: Classification, Evolution and Biodiversity. Nova Science Publishers, New York, pp. 131-151.
  • Hoek, P.P.C. (1883) Report on the Cirripedia collected by HMS 'Challenger' during the years 1873-1876. Report on the Scientific Results of the Voyage of HMS 'Challenger' during the years 1873-1876, Zoology, 8, 1-169. https://doi.org/10.5962/bhl.title.12873
  • Holmes, S.J. (1905) The Amphipoda of southern New England. Bulletin of the United States Bureau of Fisheries, 24, 457- 529.
  • Holmlund, M.B., Peterson, C.H. & Hay, M.E. (1990) Does algal morphology affect amphipod susceptibility to fish predation? Journal of Experimental Marine Biology and Ecology, 139 (1-2), 65-83. https://doi.org/10.1016/0022-0981(90)90039-F
  • Hombron, J.B. & Jacquinot, H. (1846) Crustaces. In: Voyage au pole sud et dans l'oceanie sur les corvettes l'Astrolabe et la Zelee pendant les annees 1837-1838-1839-1840 sous le commandement de M. Dumont-d'Urville capitaine de vaisseau publie par ordre du commandant de la Zelee. Zoologie. Atlas. Gide, Paris, pl. 8.
  • Hong, J.S. (1983) Three tube-building amphipods from experimental plates in Deukryang Bay in the southern coast of Korea. Korean Journal of Zoology, 26 (2), 135-153.
  • Hooper, A.K., Lehtonen, J., Schwanz, L.E. & Bonduriansky, R. (2018) Sexual competition and the evolution of condition-dependent ageing. Evolution Letters, 2 (1), 37-48. https://doi.org/10.1002/evl3.36
  • Horton, T., Lowry, J., De Broyer, C., Bellan-Santini, D., Coleman, C.O., Corbari, L., Costello, M.J., Daneliya, M., Dauvin, J.- C., Fiser, C., Gasca, R., Grabowski, M., Guerra-Garcia, J.M., Hendrycks, E., Hughes, L., Jaume, D., Jazdzewski, K., Kim, Y.-H., King, R., Krapp-Schickel, T., LeCroy, S., Lˆ rz, A.-N., Mamos, T., Senna, A.R., Serejo, C., Sket, B., Souza-Filho, J.F., Tandberg, A.H., Thomas, J.D., Thurston, M., Vader, W., Vainˆ la, R., Vonk, R., White, K. & Zeidler, W. (2020) World Amphipoda Database. Available from: http://www.marinespecies.org/amphipoda (accessed 2 February 2020) https://doi.org/10.14284/368
  • Inglis, G., Gust, N., Fitridge, I., Floerl, O., Hayden, B.J. & Fenwick, G.D. (2006a) Dunedin Harbour (Port Otago and Port Chalmers): Baseline survey for non-indigenous marine species. Biosecurity New Zealand Technical Paper No.: 2005/10. Prepared for Biosecurity New Zealand Post-Clearance Directorate for Project ZBS2000-04. MAF Information Bureau, Wellington, 67 pp.
  • Inglis, G., Gust, N., Fitridge, I., Floerl, O., Woods, C., Hayden, B.J. & Fenwick, G.D. (2006b) Port of Timaru: Baseline survey for non-indigenous marine species. Biosecurity New Zealand Technical Paper No.: 2005/06. Prepared for Biosecurity New Zealand Post-clearance Directorate for Project ZBS2000-04. MAF Information Bureau, Wellington, 61 pp.
  • Inglis, G., Gust, N., Fitridge, I., Floerl, O., Woods, C., Hayden, B.J. & Fenwick, G.D. (2006c) Whangarei Harbour (Whangarei Port and Marsden Point): Baseline survey for non-indigenous marine species. Biosecurity New Zealand Technical Paper No.: 2005/16. Prepared for Biosecurity New Zealand Post-clearance Directorate for Project ZBS2000-04. MAF Information Bureau, Wellington, 68 pp.
  • Inglis, G., Gust, N., Fitridge, I., Floerl, O., Woods, C., Kospartov, M., Hayden, B. & Fenwick, G.D. (2008) Port of Lyttelton: Second baseline survey for non-indigenous marine species. Biosecurity New Zealand Technical Paper No.: 2008/02. Prepared for MAF Biosecurity New Zealand Post Border Directorate for Project ZBS2000-04. MAF Information Bureau, Wellington, 139 pp.
  • Izquierdo, D. & Guerra-Garcίa, J.M. (2011) Distribution patterns of the peracarid crustaceans associated with the alga Corallina elongata along the intertidal rocky shores of the Iberian Peninsula. Helgoland Marine Research, 65, 233-243. https://doi.org/10.1007/s10152-010-0219-y
  • Jacobucci, G. B., Vieira, E. A. & Leite, F. P. (2019) Influence of a narrow depth gradient on the spatial structure of Sargassum peracarid assemblages in Southeastern Brazil. Marine Biodiversity, 49 (2), 1001-1011. https://doi.org/10.1007/s12526-018-0885-6
  • Jak, R. & Glorius, S.T. (2017) Macrobenthos in offshore wind farms; Areview of research, results, and relevance for future developments. Wageningen Marine Research report C043/17. Wageningen Marine Research (University & Research Centre), Wageningen, 477 pp. https://doi.org/10.18174/415357
  • Jeong, S.J., Suh, H.-L. & Kang, C.-K. (2012) Trophic diversity in amphipods within a temperate eelgrass ecosystem as determined by gut contents and Cand Nisotope analysis. Marine Biology, 159 (9), 1943-1954. https://doi.org/10.1007/s00227-012-1981-y
  • Jeong, S.J., Yu, O.H. & Suh, H.L. (2004) Seasonal variation and feeding habits of amphipods inhabiting Zostera marina beds in Gwangyang Bay, Korea. Journal of the Korean Fisheries Society, 37, 122-128. https://doi.org/10.5657/kfas.2004.37.2.122
  • Jeong, S.J., Yu, O.H. & Suh, H.L. (2006) Secondary production of Jassa slatteryi (Amphipoda, Ischyroceridae) on a Zostera marina seagrass bed in southern Korea. Marine Ecology Progress Series, 309, 205-211. https://doi.org/10.3354/meps309205
  • Jeong, S.J., Yu, O.H. & Suh, H.L. (2007) Life history and reproduction of Jassa slatteryi (Amphipoda, Ischyroceridae) on a seagrass bed (Zostera marina L.) in Southern Korea. Journal of Crustacean Biology, 27 (1), 65-70. https://doi.org/10.1651/S-2739.1
  • Johnston, G. (1829) Contributions to the British fauna. Zoological Journal, 4, 416-421.
  • Jorgensen, N.M. & Christie, H. (2003) Diurnal, horizontal and vertical dispersal of kelp-associated fauna. Hydrobiologia, 503, 69-76. https://doi.org/10.1023/B:HYDR.0000008491.89382.e5
  • Karez, R. & Ludynia, K. (2003) Niche differentiation in habitat and current preference corroborates taxonomic distinction of Jassa falcata and Jassa marmorata (Amphipoda, Crustacea). Estuarine, Coastal and Shelf Science, 58, 279-292. https://doi.org/10.1016/S0272-7714(03)00080-5
  • Kaufmann, R.S. (1994) Structure and function of chemoreceptors in scavenging lysianassoid amphipods. Journal of Crustacean Biology, 14 (1), 54-71. https://doi.org/10.1163/193724094X00470
  • Kerckhof, F., Rumes, B., Jacques, T., Degraer, S. & Norro, A. (2010a) Early development of the subtidal marine biofouling on a concrete offshore windmill foundation on the Thornton Bank (southern North Sea): first monitoring results. International Journal of the Society for Underwater Technology, 29 (3), 137-149. https://doi.org/10.3723/ut.29.137
  • Kerckhof, F., Rumes, B., Norro, A., Jacques, T.G. & Degraer, S. (2010b) Chapter 5. Seasonal variation and vertical zonation of the marine biofouling on a concrete offshore windmill foundation on the Thornton Bank (southern North Sea). In: Degraer, S., Brabant, R. & Rumes, B. (Eds.), Offshore wind farms in the Belgian part of the North Sea: Early environmental impact assessment and spatio-temporal variability. Marine Ecosystem Management Unit, Management Unit of the North Sea Mathematical Models, Belgian Institute of Natural Sciences, Brussels, pp. 53-68.
  • Khammassi, M., Jourde, J., Zaabar, W., Laabidi, S., Sauriau, P.G. & Achouri, M.S. (2019) Inventory and new records of benthic amphipods from macrophytes and fine sand communities of the Bizerte lagoon (Tunisia, SW Mediterranean Sea). Marine Biodiversity Records, 12 (1), 1-10. https://doi.org/10.1186/s41200-019-0182-5
  • Kimura M. (1980) Asimple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences. Journal of Molecular Evolution, 16, 111-120. https://doi.org/10.1007/BF01731581
  • Kodama, M., Kawamura, T., Nakamoto, K., Ohtsuchi, N., Hayakawa, J., Kitagawa, T. & Watanabe, Y. (2017) Acomparison of amphipod assemblages between canopy and understory strata in seaweed and seagrass beds off the coast of Otsuchi Bay, Japan. Biodiversity Journal, 8 (2), 471-473.
  • Kodama, M., Kawamura, T., Nakamoto, K., Ohtsuchi, N., Hayakawa, J., Kanki, T., Kitagawa, T. & Watanabe, Y. (2020) Effect of algal phenology on seasonal dynamics of gammarid assemblages: differences between canopy and understory strata in a Sargassum yezoense bed. Marine Ecology Progress Series, 634, 63-76. https://doi.org/10.3354/meps13194
  • Kodama, M. & Kawamura, T. (2019) Anew species of Bemlos Shoemaker, 1925 (Amphipoda: Aoridae) from deepwater off Tanabe Bay, Japan, with a review of the deep-sea aorids and their adaptations to the deep sea. Journal of Crustacean Biology 39 (1), 54-61. https://doi.org/10.1093/jcbiol/ruy098
  • Krapp, T., Grasso, R. & Ruffo, S. (2010) New data on the genus Jassa Leach (Amphipoda, Ischyroceridae). Zoologica Baetica, 21, 85-100.
  • Krapp, T., Rampin, M. & Libertini, A. (2008) Acytogenetical study of Ischyroceridae (Amphipoda) allows the identification of a new species, Jassa cadetta sp. n., in the Lagoon of Venice. Organisms, Diversity & Evolution, 8, 337-345. https://doi.org/10.1016/j.ode.2008.06.001
  • Krapp-Schickel, G. (1974) Camill Hellers Sammlung adriatischer Amphipoden-1866 und heute. Annalen des Naturhistorischen Museums in Wien, 78, 319-379.
  • Krapp-Schickel, G. (1993) Do algal-dwelling amphipods react to the 'critical zones' of a coastal slope? Journal of Natural History, 27, 883-900. https://doi.org/10.1080/00222939300770541
  • Krapp-Schickel, T. (2011) New antarctic stenothoids sensu lato (Amphipoda, Crustacea). European Journal of Taxonomy, 2, 1-17. https://doi.org/10.5852/ejt.2011.2
  • Krˆ ncke, I. (1994) Macrobenthos composition, abundance and biomass in the Arctic Ocean along a transect between Svalbard and the Makarov Basin. Polar Biology, 14, 519-529. https://doi.org/10.1007/BF00238221
  • Krˆ ncke, I. (1998) Macrofauna communities in the Amundsen Basin, at the Morris Jesup Rise and at the Yermak Plateau (Eurasian Arctic Ocean). Polar Biology, 19, 383-392. https://doi.org/10.1007/s003000050263
  • Krone, R., Gutowa, L., Joschko, T.J. & Schrˆ der, A. (2013) Epifauna dynamics at an offshore foundation - Implications of future wind power farming in the North Sea. Marine Environmental Research, 85, 1-12. https://doi.org/10.1016/j.marenvres.2012.12.004
  • Kumar, S., Stecher, G., Li, M., Knyaz, C. & Tamura, K. (2018) MEGA X: molecular evolutionary genetics analysis across computing platforms. Molecular Biology and Evolution, 35 (6), 1547-1549. https://doi.org/10.1093/molbev/msy096
  • Kurdziel, J. P. & Knowles, L.L. (2002) The mechanisms of morph determination in the amphipod Jassa: implications for the evolution of alternative male phenotypes. Proceedings of the Royal Society of London B, 269, 1749-1754. https://doi.org/10.1098/rspb.2002.2089
  • Laskowski, Z. & Zdzitowiecki, K. (2017) Chapter 8. Acanthocephalans in Sub-Antarctic and Antarctic. In: Klimpel, S., Kuhn, T. & Mehlhorn, H. (Eds.), Biodiversity and Evolution of Parasitic Life in the Southern Ocean. Parasitology Research Monographs. Vol. 9. Springer International Publishing, Cham, pp. 141-182. https://doi.org/10.1007/978-3-319-46343-8_8
  • Leach, W.E. (1814) Crustaceology. The Edinburgh Encyclopedia, 7, 402-404.
  • Leblanc, C., Schaal, G., Cosse, A., Destombe, C., Valero, M., Riera, P. & Potin, P. (2011) Trophic and biotic interactions in Laminaria digitata beds: which factors could influence the persistence of marine kelp forests in northern Brittany? Cahiers de Biologie Marine, 52, 415-427.
  • LeCroy, S.E. (2007) An Illustrated Identification Guide to the Nearshore Marine and Estuarine Gammaridean Amphipoda of Florida. Vol. 4. Families Anamixidae, Eusiridae, Hyalellidae, Hyalidae, Iphimediidae, Ischyroceridae, Lysianassidae, Megaluropidae and Melphidippidae. Annual Report for DEP Contract Number WM880. State of Florida, Department of Environmental Protection, Tallahassee, Florida, 614 pp.
  • LeCroy, S.E., Gasca, R., Winfield, I., Ortiz, M. & Escobar-Briones, E. (2009) Amphipoda (Crustacea) of the Gulf of Mexico. In: Felder, D.L. & Camp, D.K. (Eds.), Gulf of Mexico-Origins, Waters, and Biota. Biodiversity. Texas A&M University Press, College Station, Texas, pp. 941-972.
  • Ledoyer, M. (1986) Crustaces amphipodes gammariens, familles des Haustoriidae a Vitjazianidae. Faune de Madagascar, 59 (2), 599-1112.
  • Lefort, V., Longueville, J.-E. & Gascuel, O. (2017) SMS: Smart Model Selection in PhyML. Molecular Biology and Evolution, 34 (9), 2422-2424. https://doi.org/10.1093/molbev/msx149
  • Lewis, P.N., Bergstrom, D.M. & Whinam, J. (2006) Barging in: a temperate marine community travels to the subantarctic. Biological Invasions, 8, 787-795. https://doi.org/10.1007/s10530-005-3837-6
  • Libertini, A., Colomba, M.S. & Vitturi, R. (2000) Cytogenetics of the amphipod Jassa marmorata (Corophioidea: Ischyroceridae): karyotype morphology, chromosome banding, fluorescent in situ hybridization, and nuclear DNA content. Journal of Crustacean Biology, 20 (2), 350-356. https://doi.org/10.1163/20021975-99990046
  • Lim, B.-J. & Park, J.-Y. (2006) Redescription of Jassa slatteryi (Crustacea: Amphipoda: Ischyroceridae). Korean Journal of Environmental Biology, 24 (3), 300-305.
  • Lim, B.-J., Park, J.-Y. & Min, G.-S. (2008) New record of two species of Jassa from Korea (Crustacea: Amphipoda: Ischyroceridae). Korean Journal of Systematic Zoology, 24 (2), 219-223. https://doi.org/10.5635/KJSZ.2008.24.2.219
  • Lin, H., Wang, J., Liu, W., Liu, K., Zhang, S., He, X., Huang, Y., Lin, J., Mou, J., Zheng, C. & Yan, T. (2017) Fouling community characteristics in subtropical coastal waters of the southwestern East China Sea. Acta Oceanologica Sinica, 36 (10), 70-78. https://doi.org/10.1007/s13131-017-1007-1
  • Lincoln, R.J. (1979) British marine Amphipoda: Gammaridea. British Museum (Natural History), London, 658 pp.
  • Lobo, J., Ferreira, M.S., Antunes, I.C., Teixeira, M.A.L., Borges, L.M.S., Sousa, R., Gomes, P.A., Costa, M.H., Cunha, M.R. & Costa, F.O. (2017) Contrasting morphological and DNA barcode-suggested species boundaries among shallow-water amphipod fauna from the southern European Atlantic coast. Genome, 60, 147-157. https://doi.org/10.1139/gen-2016-0009
  • Luttikhuizen, P.C., Beermann, J., Crooijmans, R.P.M.A., Jak, R.G. & Coolen, J.W.P. (2019) Low genetic connectivity in a fouling amphipod among man-made structures in the southern North Sea. Marine Ecology Progress Series, 615, 133-142. https://doi.org/10.3354/meps12929
  • Lyons, J. & Myers, A.A. (1991) Amphipoda Gammaridea from coral rubble in the Gulf of Aqaba, Red Sea: families Dexaminidae, Eusiridae, Isaeidae, Ischyroceridae, Leucothoidae, Liljeborgiidae and Lysianassidae. Journal of Natural History, 25, 597-621. https://doi.org/10.1080/00222939100770381
  • Machado, G.B., Ferreira, A.P., Bueno, M., Siqueira, S.G. & Leite, F.P. (2019) Effects of macroalgal host identity and predation on an amphipod assemblage from a subtropical rocky shore. Hydrobiologia, 836 (1), 65-81. https://doi.org/10.1007/s10750-019-3941-8
  • Macquart-Moulin, C. (1968) Les amphipodes bentho-planctoniques du golfe de Marseille. Analyse des captures faites au cours de peches planctoniques nocturnes regulieres (annees 1963-1964). Recueil des travaux de la Station marine dʹEndoume, 43 (59), 311-332.
  • Mamos, T., Wattier, R., Burzynski, A. & Grabowski, M. (2016) The legacy of a vanished sea: a high level of diversification within a European freshwater amphipod species complex driven by 15 My of Paratethys regression. Molecular Ecology, 25 (3), 795-810. https://doi.org/10.1111/mec.13499
  • Mangano, M.C., Ape, F. & Mirto, S. (2019) The role of two non-indigenous serpulid tube worms in shaping artificial hard substrata communities: case study of a fish farm in the central Mediterranean Sea. Aquaculture Environment Interactions, 11, 41-51. https://doi.org/10.3354/aei00291
  • Marchini, A. & Cardeccia, A. (2017) Alien amphipods in a sea of troubles: cryptogenic species, unresolved taxonomy and overlooked introductions. Marine Biology, 164, 164-169. https://doi.org/10.1007/s00227-017-3093-1
  • Marchini, A., Ragazzola, F., Vasapollo, C., Castelli, A., Cerrati, G., Gazzola, F., Jiang, C., Langeneck, J., Manauzzi, M.C., Musco, L., Nannini, M., Zekonyte, J. & Lombardi, C. (2019) Intertidal Mediterranean coralline algae habitat is expecting a shift toward a reduced growth and a simplified associated fauna under climate change. Frontiers in Marine Science, 6, 106. https://doi.org/10.3389/fmars.2019.00106
  • Martinez-Laiz, G., Ulman, A., Ros, M. & Marchini, A. (2019) Is recreational boating a potential vector for non-indigenous peracarid crustaceans in the Mediterranean Sea? Acombined biological and social approach. Marine Pollution Bulletin, 140, 403-415. https://doi.org/10.1016/j.marpolbul.2019.01.050
  • Mavraki, N., Degraer S. & Vanaverbeke, J. (2019) Feeding behaviour of seven important fouling species: The key to their success? In: Mees, J. & Seys, J. (Eds.), 2019. Book of abstracts-VLIZ Marine Science Day. Bredene, Belgium, 13 March 2019. VLIZ Special Publication 83. Vlaams Instituut voor de Zee-Flanders Marine Institute (VLIZ), Oostende, Belgium, p. 121.
  • McCain, J.C. (1968) The Caprellidae (Crustacea: Amphipoda) of the Western North Atlantic. Bulletin of the United States National Museum, 278, 1-145. https://doi.org/10.5962/bhl.part.8960
  • McCollin, T. & Brown, L. (2014) Native and non native marine biofouling species present on commercial vessels using Scottish dry docks and harbours. Management of Biological Invasions, 5 (2), 85-96. https://doi.org/10.3391/mbi.2014.5.2.02
  • Miller, J.A., Gillman, R., Carlton, J.T., Murray, C.C., Nelson, J.C., Otani, M. & Ruiz, G.M. (2018) Trait-based characterization of species transported on Japanese tsunami marine debris: Effect of prior invasion history on trait distribution. Marine Pollution Bulletin, 132, 90-101. https://doi.org/10.1016/j.marpolbul.2017.12.064
  • Miller, J.A., Carlton, J.T., Chapman, J.W., Geller, J.B. & Ruiz, G.M. (2019a) Chapter 11: Survival and fitness of Japanese Tsunami Marine Debris rafting species. In: Clarke Murray, C., Therriault, T.W., Maki, H. & Wallace, N. (Eds.), The Effects of Marine Debris Caused by the Great Japan Tsunami of 2011. PICES Special Publication, 6, Sidney, British Columbia, Canada, pp. 169-176. Available from: https://core.ac.uk/download/pdf/286777757.pdf (accessed 20 January 2021)
  • Miller, J.A., Gillman, R., Carlton, J.T., Murray, C., Nelson, J.C., Otani, M. & Ruiz, G.M. (2019b) Chapter 12: Distributional, environmental, and life history attributes of Japanese Tsunami Marine Debris biota. In: Clarke Murray, C., Therriault, T.W., Maki, H. & Wallace, N. (Eds.), The Effects of Marine Debris Caused by the Great Japan Tsunami of 2011. PICES Special Publication 6. pp. 179-194. Available from: https://core.ac.uk/download/pdf/286777757.pdf (accessed 20 January 2021)
  • Miller, M.A., Pfeiffer, W. & Schwartz, T. (2010) Creating the CIPRES Science Gateway for inference of large phylogenetic trees. In: Gateway Computing Environments (Eds.), 2010 Gateway Computing Environments Workshop (GCE), New Orleans, Louisiana, 14 November 2010, pp. 1-8. https://doi.org/10.1109/GCE.2010.5676129
  • Monod, T. (1926) Tanaidaces, Isopodes et Amphipodes. In: Commission de la "Belgica" (corp. auth.), Expedition Antarctique Belge: Resultats du Voyage de la Belgica en 1897-1899 Sous le Commandement de A. de Gerlache de Gomery (Zoology). J.-E. Buschmann, Anvers, pp. 1-67.
  • Montagu, G. (1808) Description of several marine animals found on the south coast of Devonshire. Transactions of the Linnean Society of London, 9, 81-114. https://doi.org/10.1111/j.1096-3642.1818.tb00327.x
  • Montes, C., Cardona, A., Jaramillo, C., Pardo, A., Silva, J.C., Valencia, V., Ayala, C., Perez-Angel, L.C., Rodriguez-Parra, L.A., Ramirez, V. & Nino, H. (2015) Middle Miocene closure of the Central American seaway. S cience, 348 (6231), 226-229. https://doi.org/10.1126/science.aaa2815
  • Moore, P.G. (1973) The larger Crustacea associated with holdfasts of kelp (Laminaria hyperborea) in North-East Britain. Cahiers de Biologie Marine, 14, 493-518.
  • Moore, P.G. & Eastman, L.B. (2015) The tube-dwelling lifestyle in crustaceans and its relation to feeding. In: Thiel, M. & Watling, L. (Eds.), The Natural History of the Crustacea. Vol. 2. Oxford University Press, New York, New York, pp. 35-77.
  • Morino, H. (2019) List of amphipod type specimens relocated in the collection of the National Museum of Nature and Science, Tsukuba, Japan. Bulletin of the National Museum of Nature and Science, Series A, 45 (2), 39-43.
  • Moshchenko, A.V. & Zvyagintsev, A.U. (2004) Composition, structure and some distribution features of fouling community in the water intake tunnel of Vladivostok Heat and Power Plant. Ocean and Polar Research, 26 (4), 619-633. https://doi.org/10.4217/OPR.2004.26.4.619
  • Moshchenko, A.V. & Zvyagintsev, A.U. (2010) Macrofouling communities in the cooling system of the Vladivostok Heat and Power Plant. Ocean Science Journal, 45 (1), 41-54. https://doi.org/10.1007/s12601-010-0004-5
  • Mulayim, A., Arysal, S.B. & Balkys, H. (2015a) Distribution, diversity and some ecological characteristics of benthic amphipods in the Kapidad Peninsula (Marmara Sea, Turkey). Oceanological and Hydrological Studies, 44 (1), 28-37. https://doi.org/10.1515/ohs-2015-0004
  • Mulayim, A., Balkis, H. & Sezgin, M. (2015b) Benthic amphipod (Crustacea) fauna of the Bandyrma and Erdek Gulfs and some environmental factors affecting their distribution. Acta Adriatica, 56 (2), 171-188.
  • Murray, J. & Thomson, C.W. (1895) Report on the Scientific Results of the Voyage of HMS Challenger During the Years 1873-76 under the Command of Captain George S. Nares and the Late Captain Frank Tourle Thomson: Asummary of the scientific results. Printed for HM Stationery Office, London, LIV + XIX + 1608 + VIII + 32 pp.
  • Nagle, J.S. (1968) Distribution of the epibiota of macroepibenthic plants. Contributions in Marine Science, 13, 105-144.
  • Nair, K.C.C. & Anger, K. (1979) Experimental studies on the life cycle of Jassa falcata (Crustacea, Amphipoda). Helgolander wissenschaftliche Meeresuntersuchungen, 32, 444-452. https://doi.org/10.1007/BF02277988
  • Nall, C.R., Guerin, A.J. & Cook, E.J. (2015) Rapid assessment of marine non-native species in northern Scotland and a synthesis of existing Scottish records. Aquatic Invasions, 10 (1), 107-121. https://doi.org/10.3391/ai.2015.10.1.11
  • Nardo, G.D. (1847a) Prospetto della fauna marina volgare del Veneto Estuario con cenni sulle principali specie commestibili dell'Adriatico, sulle venete pesche, sulle valli, ecc. In: Privil, I.R. (Ed.), Venezia e le Sue Lagune. Vol. 2. G. Antonelli, Venezia, pp. 113-156.
  • Nardo, G.D. (1847b) Sinonimia moderna delle specie registrate nell' opera intitolata: descrizione de' crostacei, de' testacei e de' pesci che abitano le lagune e golfo Veneto rappresentanti in figure, a chiaro-scuro ed a colori dall' Abate Stefano Chiereghini: Venezia, Ven. Clodiense, applicata per commissione governativa dal Dr. Gio. Domenico Nardo. G. Antonelli, Venezia, 127 pp. https://doi.org/10.5962/bhl.title.120206
  • Nardo, G.D. (1869) Annotazioni illustranti cinquantaquattro specie di Crostacei podottalmi, endottalmi e succinatori del Mare Adriatico: Alcune delle quali nuove o male conosciute, accompagnate de trentatre figure litografate, e precedute dall storia della carcinologia Adriatica antica e recente. Memorie del Instituto Veneto, 14, 217-340. https://doi.org/10.5962/bhl.title.120193
  • Navarro-Barranco, C., Guerra-Garcia, J.M., Sanchez-Tocino, L., Ros, M., Florido, M., Garcia-Gomez, J.C. (2015) Colonization and successional patterns of a mobile epifaunal community along an environmental gradient in a marine cave. Marine Ecology Progress Series, 521, 105-115. https://doi.org/10.3354/meps11126
  • Navarro-Barranco, C., Munoz-Gomez, B., Saiz, D., Ros, M., Guerra-Garcia, J.M., Altamirano, M., Ostale-Valriberas, E. & Moreira, J. (2019) Can invasive habitat-forming species play the same role as native ones? The case of the exotic marine macroalga Rugulopteryx okamurae in the Strait of Gibraltar. Biological Invasions, 21 (11), 3319-3334. https://doi.org/10.1007/s10530-019-02049-y
  • Nebeski, O. (1880) Beitrage zur Kenntniss der Amphipoden der Adria. In: Claus, C. (Ed.), Arbeiten aus dem Zoologischen Institute Der Universitat Wien und der Zoologischen Station in Triest. Vol. 3. Alfred Holder, Wien, pp. 1-52.
  • Needham, A.E. (1970) Integumental pigments of the amphipod, Jassa. Nature, 228 (5278), 1336-1337. https://doi.org/10.1038/2281336a0
  • Neretin, N.Y., Zhadan, A.E. & Tzetlin, A.B. (2017) Aspects of mast building and the fine structure of "amphipod silk" glands in Dyopedos bispinis (Amphipoda, Dulichiidae). Contributions to Zoology, 86 (2), 145-168. https://doi.org/10.1163/18759866-08602003
  • Norderhaug, K.M. (2004) Use of red algae as hosts by kelp-associated amphipods. Marine Biology, 144, 225-230. https://doi.org/10.1007/s00227-003-1192-7
  • Norderhaug, K.M., Christie, H., Fossa, J.H. & Fredriksen, S. (2005) Fish-macrofauna interactions in a kelp (Laminaria hyperborea) forest. Journal of the Marine Biological Association of the U.K., 85, 1279-1286. https://doi.org/10.1017/S0025315405012439
  • Norderhaug, K.M., Christie, H. & Rinde, E. (2002) Colonisation of kelp imitations by epiphyte and holdfast fauna; a study of mobility patterns. Marine Biology, 141, 965-973. https://doi.org/10.1007/s00227-002-0893-7
  • Norderhaug, K.M., Fredriksen, S. & Nygaard, K. (2003) Trophic importance of Laminaria hyperborea to kelp forest consumers and the importance of bacterial degradation to food quality. Marine Ecology Progress Series, 255, 135-144. https://doi.org/10.3354/meps255135
  • Norman, A.M. (1905) VIII.-Revised nomenclature of the species described in Bate and Westwood's 'British Sessile-eyed Crustacea'. Journal of Natural History, 16 (91), 78-95. https://doi.org/10.1080/03745480509443653
  • O'Dea, A., Jackson, J.B.C., Fortunato, H., Smith, J.T., D'Croz, L., Johnson, K.G. & Todd, J.A. (2007) Environmental change preceded Caribbean extinction by 2 million years. Proceedings of the National Academy of Sciences of the United States of America, 104 (13), 5501-5506. https://doi.org/10.1073/pnas.0610947104
  • Pacios, I., Guerra-Garcia, J.M., Baeza-Rojano, E. & Cabezas, M.P. (2011) The non-native seaweed Asparagopsis armata supports a diverse crustacean assemblage. Marine Environmental Research, 71, 275e282. https://doi.org/10.1016/j.marenvres.2011.02.002
  • Pappalardo, P., Pringle, J.M., Wares, J.P. & Byers, J.E. (2015) The location, strength, and mechanisms behind marine biogeographic boundaries of the east coast of North America. Ecography, 38 (7), 722-731. https://doi.org/10.1111/ecog.01135
  • Pavia, H., Carr, H. & Aberg, P. (1999) Habitat and feeding preferences of crustacean mesoherbivores inhabiting the brown seaweed Ascophyllum nodosum (L.) Le Jol. and its epiphytic macroalgae. Journal of Experimental Marine Biology and Ecology, 236 (1), 15-32. https://doi.org/10.1016/S0022-0981(98)00191-9
  • Paz-Rios, C.E. & Ardisson, P.L. (2013) Benthic amphipods (Amphipoda: Gammaridea and Corophiidea) from the Mexican southeast sector of the Gulf of Mexico: checklist, new records and zoogeographic comments. Zootaxa, 3635 (2), 137- 173. https://doi.org/10.11646/zootaxa.3635.2.4
  • Pequegnat, W.E. & Pequegnat, L.H. (1968) Ecological Aspects of Marine Fouling in the Northeastern Gulf Of Mexico. No. A/M-Ref-68-22t. Texas A & M University, College Station, Texas, 88 pp.
  • Peters, K., Sink, K. & Robinson, T.B. (2019) Aliens cruising in: Explaining alien fouling macro-invertebrate species numbers on recreational yachts. Ocean & Coastal Management, 182, 104986. https://doi.org/10.1016/j.ocecoaman.2019.104986
  • Pfeffer, G. (1888) Die krebse von Sud-Georgien nach der ausbeute der Deutschen station 1882-83. 2. Die Amphipoden. Hamburg Wissenschafftlichen Anstalten Jahrbuch, 5, 75-142. https://doi.org/10.5962/bhl.title.10084
  • Philbrick, N. (2004) Sea of Glory: America's Voyage of Discovery: the US Exploring Expedition, 1838-1842. Penguin, New York, 451 pp.
  • Pilgrim, E.M. & Darling, J.A. (2010) Genetic diversity in two introduced biofouling amphipods (Ampithoe valida & Jassa marmorata) along the Pacific North American coast: investigation into molecular identification and cryptic diversity. Diversity and Distributions, 16, 827-839. https://doi.org/10.1111/j.1472-4642.2010.00681.x
  • Piola, R. & Conwell, C. (2010) Vessel biofouling as a vector for the introduction of non-indigenous marine species to New Zealand: Fishing vessels. Biosecurity New Zealand Technical Paper No.: 2010/11. Prepared for Biosecurity New Zealand Post-clearance Directorate for Project 08-10840. 57 pp. Available from: https://www.mpi.govt.nz/dmsdocument/7335/direct (accessed 20 January 2021)
  • Plaisance, L., Brainard, R., Caley, M.J. & Knowlton, N. (2011a) Using DNA barcoding and standardized sampling to compare geographic and habitat differentiation of crustaceans: A Hawaiian Islands example. Diversity, 4, 581-591. https://doi.org/10.3390/d3040581.
  • Plaisance, L., Caley, M.J., Brainard, R.E. & Knowlton, N. (2011b) The diversity of coral reefs: What are we missing? PLoS ONE, 6 (10), e25026. https://doi.org/10.1371/journal.pone.0025026
  • Ponti, M., Grech, D., Mori, M., Perlini, R.A., Ventra, V., Panzalis, P.A. & Cerrano, C. (2016) The role of gorgonians on the diversity of vagile benthic fauna in Mediterranean rocky habitats. Marine Biology, 163, 120. https://doi.org/10.1007/s00227-016-2897-8
  • Pulfrich, A. & Griffiths, C.L. (1988) Feeding biology of the hottentot, Pachymetopon blochii (Val.), with an estimate of daily ration. African Zoology, 23 (3), 196-207. https://doi.org/10.1080/02541858.1988.11448102
  • Rambaut, A., Drummond, A.J, Xie, D., Baele, G. & Suchard, M.A. (2018) Posterior summarisation in Bayesian phylogenetics using Tracer 1.7. Systematic Biology, 67 (5), 901-904. https://doi.org/10.1093/sysbio/syy032
  • Rathke, H. (1843) Beitrage zur fauna Norwegens. Nova Acta Academiae Caesareae Leopoldino-Carolinae Naturae Curiosorum, Breslau & Bonn, 20, 1-264. https://doi.org/10.5962/bhl.title.120119
  • Raz-Guzman, A. & Soto, L.A. (2017) Updated checklist and zoogeographic remarks of benthic amphipods (Crustacea: Peracarida: Amphipoda) of two coastal lagoons in the western Gulf of Mexico. Revista Mexicana de Biodiversidad, 88 (3), 715-734. https://doi.org/10.1016/j.rmb.2017.07.002
  • Relini, G., Relini, M. & Montanari, M. (2000) An offshore buoy as a small artificial island and a fish-aggregating device (FAD) in the Mediterranean. Hydrobiologia, 440 (1-3), 65-80. https://doi.org/10.1023/A:1004101215965
  • Reubens, J., Degraer, S. & Vincx, M. (2010) The importance of marine wind farms, as artificial hard substrata, for the ecology of the ichthyofauna. In: Degraer, S., Brabant, R. & Rumes, B. (Eds.), Offshore wind farms in the Belgian part of the North Sea: Early environmental impact assessment and spatio-temporal variability. Marine Ecosystem Management Unit, Management Unit of the North Sea Mathematical Models, Belgian Institute of Natural Sciences, Brussels, pp. 69-82.
  • Reubens, J.T., Degraer, S. & Vincx, M. (2014a) The ecology of benthopelagic fishes at offshore wind farms: a synthesis of 4 years of research. Hydrobiologia, 727 (1), 121-136. https://doi.org/10.1007/s10750-013-1793-1
  • Reubens, J.T., De Rijcke, M., Degraer, S. & Vincx, M. (2014b) Diel variation in feeding and movement patterns of juvenile Atlantic cod at offshore wind farms. Journal of Sea Research, 85, 214-221. https://doi.org/10.1016/j.seares.2013.05.005
  • Reubens, J.T., Vandendriessche, S., Zenner, A.N., Degraer, S. & Vincx, M. (2013) Offshore wind farms as productive sites or ecological traps for gadoid fishes?-Impact on growth, condition index and diet composition. Marine Environmental Research, 90, 66-74. https://doi.org/10.1016/j.marenvres.2013.05.013
  • Riera, R., Ramos, E., Herrera, R. & Moro, L. (2014) Jassa marmorata (Holmes, 1905) and Monocorophium acherusicum (Costa, 1853) new amphipods (Crustacea: Amphipoda) to the Canary Islands. Revista de la Academia Canaria de Ciencias, 26, 27-31.
  • Ros, M., Navarro-Barranco, C., Gonzalez-Sanchez, M., Ostale-Valriberas, E., Cervera-Currado, L. & Guerra-Garcia, J.M. (2020) Starting the stowaway pathway: the role of dispersal behavior in the invasion success of low-mobile marine species. Biological Invasions, 22, 2797-2812. https://doi.org/10.1007/s10530-020-02285-7
  • Roxburgh, S.H., Shea, K. & Wilson, J.B. (2004) The intermediate disturbance hypothesis: patch dynamics and mechanisms of species coexistence. Ecology, 85 (2), 359-371. https://doi.org/10.1890/03-0266
  • Rumbold, C., Lancia, J., Vazquez, G., Albano, M., Farias, N., Moyano, M.P.S., Spivak, E. & Obenat, S. (2015a) Morphological and genetic confirmation of Jassa slatteryi (Crustacea: Amphipoda) in a harbour of Argentina. Marine Biodiversity Records, 8, 1-5. https://doi.org/10.1017/S1755267215000135
  • Rumbold, C.E., Obenat, S.M., Leonardi, M.S. & Spivak, E.D. (2015b) Intersex in the gonochoristic crustacean Tanais dulongii (Audouin, 1826) (Peracarida: Tanaidacea: Tanaididae): a comparison of external reproductive characteristics. Journal of Natural History, 49 (13-14), 775-788. https://doi.org/10.1080/00222933.2014.981309
  • Sano, M., Omori, M. & Taniguchi, K. (2003) Predator-prey systems of drifting seaweed communities off the Tohoku coast, northern Japan, as determined by feeding habitat analysis of phytal animals. Fisheries Science, 69, 260-268.
  • Sars, G.O. (1894) Amphipoda. Part XXVII & XXVIII. Podoceridae (concluded), Corophiidae, Cheluridae. An account of the Crustacea of Norway, with short descriptions and figures of all the species, 1, 589-628. https://doi.org/10.5962/bhl.title.1164
  • Schaal, G., Lecler, J.-C., Droual, G., Leroux, C. & Rierad, P. (2016) Biodiversity and trophic structure of invertebrate assemblages associated with understorey red algae in a Laminaria digitata bed. Marine Biology Research, 12 (5), 513-523. https://doi.org/10.1080/17451000.2016.1164318
  • Schejter, L., Rimondino, C., Chiesa, I., Diaz de Astarloa, J.M., Doti, B., Elias, R., Escolar, M., Genzano, G., Lopez-Gappa, J., Tatian, M., Zelaya, D.G., Cristobo, J., Perez, C.D., Cordeiro, R.T. & Bremec, C.S. (2016) Namuncura Marine Protected Area: an oceanic hot spot of benthic biodiversity at Burdwood Bank, Argentina. Polar Biology, 39, 2373-2386. https://doi.org/10.1007/s00300-016-1913-2
  • Schellenberg, A. (1926) Die Gammariden der Deutschen Sudpolar-Expedition 1901-1903. Deutsche Sudpolar-Expedition 1901-1903, 18 (10), 235-414.
  • Schuckel, U., Schuckel, S., Beck, M. & Liebezeit, G. (2010) New range expansion of Caprella mutica Schurin, 1935 (Malacostraca: Caprellidae) to the German coast, North Sea. Aquatic Invasions, 5 (1), S85-S89. https://doi.org/10.3391/ai.2010.5.S1.018
  • Schurin, A. (1935) Zur fauna der caprelliden in der Bucht Peters des Grossen (Japanisches Meer). Zoologischer Anzeiger 122, 198-203.
  • Schwindt, E., Carlton, J.T., Orensanz, J.M., Scarabino, F. & Bortolus, A. (2020) Past and future of the marine bioinvasions along the Southwestern Atlantic. Aquatic Invasions, 15 (1), 11-29. https://doi.org/10.3391/ai.2020.15.1.02.
  • Scinto, A., Benvenuto, C., Cerrano, C. & Mori, M. (2007) Seasonal cycle of Jassa marmorata Holmes, 1905 (Amphipoda) in the Ligurian Sea (Mediterranean, Italy). Journal of Crustacean Biology, 27 (2), 212-216. https://doi.org/10.1651/S-2693.1
  • Sebens, K.P. (1985) Chapter 23. Community ecology of vertical rock walls in the Gulf of Maine, U.S.A.: Small-scale processes and alternative community states. In: Moore, P.G. & Seed, R. (Eds.), The Ecology of Rocky Coasts. Hutchinson, London, pp. 346-371.
  • Sedano, F., de Figueroa, J.T., Navarro-Barranco, C., Ortega, E., Guerra-Garcia, J.M. & Espinosa, F. (2020a) Do artificial structures cause shifts in epifaunal communities and trophic guilds across different spatial scales? Marine Environmental Research, 158, 104998. https://doi.org/10.1016/j.marenvres.2020.104998
  • Sedano, F., Navarro-Barranco, C., Guerra-Garcia, J.M. & Espinosa, F. (2020b) From sessile to vagile: Understanding the importance of epifauna to assess the environmental impacts of coastal defence structures. Estuarine, Coastal and Shelf Science, 235, 106616. https://doi.org/10.1016/j.ecss.2020.106616
  • Sensurat-Genc, T., Akyol, O., Ozgul, A. & Ozden, U. (2019) Food composition of whiting Merlangius merlangus, captured around the sea-cage fish farms in Ordu, south-eastern Black Sea. Journal of the Marine Biological Association of the United Kingdom, 99 (7), 1651-1659. https://doi.org/10.1017/S0025315419000626
  • Sexton, E.W. & Reid, D.M. (1951) The life-history of the multiform species Jassa falcata (Montagu) (Crustacea Amphipoda) with a review of the bibliography of the species. Journal of the Linnean Society of London, Zoology, 42, 283, 29-91. https://doi.org/10.1111/j.1096-3642.1951.tb01852.x
  • Sheldon, C.M., Seidenkrantz, M.S., Pearce, C., Kuijpers, A., Hansen, M.J. & Christensen, E.Z. (2016) Holocene oceanographic changes in SW Labrador Sea, off Newfoundland. The Holocene, 26 (2), 274-289. https://doi.org/10.1177/0959683615608690
  • Short, S., Yang, G., Kille, P. & Ford, A.T. (2012) Awidespread and distinctive form of amphipod intersexuality not induced by known feminising parasites. Sexual Development, 6, 320-324. https://doi.org/10.1159/000343779
  • Siqueira, S.G.L., Cravo, A., Leite, F.P.P. & Amaral, A.C.Z. (2017) Macrofauna associated with the bryozoan Biflustra grandicella (Canu et Bassler, 1929) on the Brazilian coast. Biodiversity Journal, 8 (2), 653-654.
  • Sirenko, B., Denisenko, S., Deubel, H. & Rachor, E. (2004) Deep water communities of the Laptev Sea and adjacent parts of the Arctic Ocean. Russian Academy of Sciences, Zoological Institute. Explorations of the Fauna of the Seas, 54 (62), 28-73.
  • Slavik, K., Lemmen, C., Zhang, W., Kerimoglu, O., Klingbeil, K. & Wirtz, K.W. (2019) The large-scale impact of offshore wind farm structures on pelagic primary productivity in the southern North Sea. Hydrobiologia, 845 (1), 35-53. https://doi.org/10.1007/s10750-018-3653-5
  • Stebbing, T.R.R. (1888) Report on the Amphipoda collected by HMS 'Challenger' during the years 1873-1876. Report on the Scientific Results of the Voyage of HMS 'Challenger' during the years 1873-1876, Zoology, 29, 1-1737.
  • Stebbing, T.R.R. (1899a) XXXVII.-On the true Podocerus and some new genera of amphipods. Annals and Magazine of Natural History, Series 7, 3 (15), 237-241. https://doi.org/10.1080/00222939908678113
  • Stebbing, T.R.R. (1899b) XVIII.-Revision of Amphipoda (continued). Annals and Magazine of Natural History, Series 7, 4 (21), 205-211. https://doi.org/10.1080/00222939908678185
  • Stebbing, T.R.R. (1906) Amphipoda. I. Gammaridea. Das Tierreich, 21, 1-806.
  • Stebbing, T.R.R. & Fowler, G.H. (1904) Biscayan Plankton. Part II.-The Amphipoda and Cladocera, with notes on a larval thyrostracan. Transactions of the Linnean Society of London, Zoology, Series 2, 10 (2), 13-54. https://doi.org/10.1111/j.1096-3642.1904.tb00180.x
  • Steele, V.J. & Steele, D.H. (1997) Type II microtrich sensilla of amphipods: variations in external morphology and distributional patterns. Canadian Journal of Zoology, 75 (7), 1155-1165. https://doi.org/10.1139/z97-138
  • Steele, V.J. & Steele, D.H. (1999) Cellular organization and fine structure of type II microtrich sensilla in gammaridean amphipods (Crustacea). Canadian Journal of Zoology, 77 (1), 88-107. https://doi.org/10.1139/z98-185
  • Stenberg, C., Stottrup, J.G., van Deurs, M., Berg, C.W., Dinesen, G.E., Mosegaard, H., Grome, T.M. & Leonhard, S.B. (2015) Long-term effects of an offshore wind farm in the North Sea on fish communities. Marine Ecology Progress Series, 528, 257-265 https://doi.org/10.3354/meps11261
  • Stephensen, K. (1949) The Amphipoda of Tristan da Cunha. Results of the Norwegian Scientific Expedition to Tristan da Cunha 1937-1938, 3 (19), 1-61.
  • Stoner, A.W. (1980) Perception and choice of substratum by epifaunal amphipods associated with seagrasses. Marine Ecology Progress Series, 3 (10), 105-111. https://doi.org/10.3354/meps003105
  • Strong, J.A., Maggs, C.A. & Johnson, M.P. (2009) The extent of grazing release from epiphytism for Sargassum muticum (Phaeophyceae) within the invaded range. Journal of the Marine Biological Association of the United Kingdom, 89 (2), 303-314. https://doi.org/10.1017/S0025315408003226
  • Sudo, H. & Azeta, M. (1996) Life history and production of the amphipod Byblis japonicus Dahl (Gammaridea: Ampeliscidae) in a warm temperate zone habitat, Shijiki Bay, Japan. Journal of Experimental Marine Biology and Ecology, 198, 203-222. https://doi.org/10.1016/0022-0981(96)00012-3
  • Suwandy, J. (2012) Temporal Currency: Life-history Strategies of a Native Marine Invertebrate Increasingly Exposed to Urbanisation and Invasion. M.Sc. Thesis, University of Canterbury, Christchurch, 119 pp.
  • Switzer, S.E. (2010) Invertebrate fouling community composition associated with Pacific oyster (Crassostrea gigas) suspended tray culture. The University Of British Columbia, Vancouver, British Columbia, 76 pp.
  • Tanaka, M.O. & Leite, F.P. (2004) Distance effects on short-term recolonization of Sargassum stenophyllum by mobile epifauna, with an analysis of gammarid life habits. Journal of the Marine Biological Association of the United Kingdom, 84 (5), 901-910. https://doi.org/10.1017/S0025315404010173h
  • Thiel, M. (2011) Chapter 10. Chemical communication in peracarid crustaceans. In: Breithaupt, T. & Thiel, M. (Eds.), Chemical Communication in Crustaceans. Springer, New York, New York, pp. 199-218. https://doi.org/10.1007/978-0-387-77101-4_10
  • Thomson, G.M. (1883) General notes. Podocerus validus, Dana. New Zealand Journal of Science, 1 (11), 517.
  • Thurston, M.H. (1974) The Crustacea Amphipoda of Signy Island, South Orkney Islands. British Antarctic Survey Scientific Reports, 71, 1-133.
  • Tisch, N. (1997) Ecology and Evolution of Life History Variation in the Marine Amphipod Jassa marmorata Holmes. UMI Microform 9831122. Ph.D. Thesis, University of Rhode Island, Kingston, Rhode Island, 156 pp.
  • Ulman, A., Ferrario, J., Occhpinti-Ambrogi, A., Arvanitidis, C., Bandi, A., Bertolino, M., Bogi, C., Chatzigeorgiou, G., Cicek, B.A., Deidun, A., Ramos-Espla, A., Kocak, C., Lorenti, M., Martinez-Laiz, G., Merlo, G., Princisgh, E., Scribano, G. & Marchini, A. (2017) Amassive update of non-indigenous species records in Mediterranean marinas. PeerJ, 5, e3954. https://doi.org/10.7717/peerj.3954
  • Ulrich, I., Anger, K. & Schttler, U. (1995) Tube-building in two epifaunal amphipod species, Corophium insidiosum and Jassa falcata. Helgolander Meeresuntersuchungen, 49 (1), 393-398. https://doi.org/10.1007/BF02368364
  • Vader, W. & Krapp, T. (2005) Crab-associated amphipods from the Falkland Islands (Crustacea, Peracarida). Journal of Natural History, 39, 3075-3099. https://doi.org/10.1080/00222930500218573
  • Vader, W. & Tandberg, A.H.S. (2015) Amphipods as associates of other Crustacea: a survey. Journal of Crustacean Biology, 35 (4), 522-532. https://doi.org/10.1163/1937240X-00002343
  • Valentine, P., Carman, M.R. & Blackwood, D. (2016) Observations of recruitment and colonization by tunicates and associated invertebrates using giant one-meter2 recruitment plates at Woods Hole, Massachusetts. Management of Biological Invasions, 7 (1), 115-130. https://doi.org/10.3391/mbi.2016.7.1.14
  • Valerio-Berardo, M.T. & Flynn, M.N. (2002) Composition and seasonality of an amphipod community assoiated to the algae Bryocladia trysigera. Brazilian Journal of Biology, 62 (4A), 735-742. https://doi.org/10.1590/S1519-69842002000400021
  • Ventura, D., Bonhomme, V., Colangelo, P., Bonifazi, A., Lasinio, G.J. & Ardizzone, G. (2017) Does morphology predict trophic niche differentiation? Relationship between feeding habits and body shape in four co-occurring juvenile species (Pisces: Perciformes, Sparidae). Estuarine, Coastal and Shelf Science, 191, 84-95. https://doi.org/10.1016/j.ecss.2017.04.014
  • Viejo, R.M. (1999) Mobileepifaunainhabitingtheinvasive Sargassum muticum andtwolocal seaweedsinnorthern Spain. Aquatic Botany, 64 (2), 131-149. https://doi.org/10.1016/S0304-3770(99)00011-X
  • Wada, T., Yamada, T., Shimizu, D., Aritaki, M., Sudo, H., Yamashita, Y. & Tanaka, M. (2010) Successful stocking of a depleted species, spotted halibut Verasper variegatus, in Miyako Bay, Japan: evaluation from post-release surveys and landings. Marine Ecology Progress Series, 407, 243-255. https://doi.org/10.3354/meps08553
  • Wakabara, Y., Tararam, A.S. & Takeda, A.M. (1983) Comparative study of the amphipod fauna living on Sargassum of two Itanhaem shores, Brazil. Journal of Crustacean Biology, 3 (4), 602-607. https://doi.org/10.1163/193724083X00265
  • Walker, A.O. (1893) Podocerus herdmani, n. sp., In: Herdman, W.A., Sixth annual report of the Liverpool Marine Biology Committee and their biological station at Port Erin. P roceedings and Transactions of the Liverpool Biological Society. The Society, Liverpool, 1893, p. 79.
  • Walker, A.O. (1903) Amphipoda of the "Southern Cross" Antarctic Expedition. Journal of the Linnean Society of London, Zoology, 29 (187), 38-64. https://doi.org/10.1111/j.1096-3642.1903.tb00425.x
  • Walker, A.O. (1907) Crustacea. III. -Amphipoda. National Antarctic Expedition 1901-1904. Natural History, 3, 1-39.
  • Walker, A.O. (1911) Notes on Jassa falcata (Mont.). Transactions of the Liverpool Biological Society, 25, 67-72.
  • Wanless, R.M., Scott, S., Sauer, W.H.H., Andrew, T.G., Glass, J.P., Godfrey, B., Griffiths, C. & Yeld, E. (2010) Semi-submersible rigs: a vector transporting entire marine communities around the world. Biological Invasions, 12, 2573-2583. https://doi.org/10.1007/s10530-009-9666-2
  • White, C.A. (2017) Aquaculture-derived terrestrial fatty acids in marine food webs. Ph. D. Thesis, School of BioSciences, University of Melbourne, Melbourne, 237 pp. http://hdl.handle.net/11343/129829
  • Wichmann, C.S., Hinojosa, I.A. & Thiel, M. (2012) Floating kelps in Patagonian Fjords: an important vehicle for rafting invertebrates and its relevance for biogeography. Marine Biology, 159 (9), 2035-2049. https://doi.org/10.1007/s00227-012-1990-x
  • Wilber, D.H., Clarke, D.G., Ray, G.L. & Burlas, M. (2003) Response of surf zone fish to beach nourishment operations on the northern coast of New Jersey, USA. Marine Ecology Progress Series, 250, 231-246. https://doi.org/10.3354/meps250231
  • Winfield I., Herrera-Dorantes M.T. & Ardisson, P.L. (2021) Distribution of genus Jassa (Amphipoda, Ischyroceridae) in the Bay of Campeche, SW Gulf of Mexico, with a description of a new deepwater species. Bulletin of Marine Science, 97 (1), 219-236. https://doi.org/10.5343/bms.2020.0042
  • Yasumoto, S. & Nagasawa, K. (1996) Possible life cycle of Longicollum pagrosomi, an acanthocephalan parasite of cultured red sea bream. Fish Pathology, 31 (4), 235-236. https://doi.org/10.3147/jsfp.31.235
  • Yu, O.H., Soh, H.Y. & Suh, H.-L. (2002) Seasonal zonation patterns of benthic amphipods in a sandy shore surf zone of Korea. Journal of Crustacean Biology, 22 (2), 459-466. https://doi.org/10.1163/20021975-99990253
  • Yu, O.H., Jeong, S.J., Kim, D., Lee, J.-H. & Suh, H.-L. (2009) Seasonal variation in diel and tidal effects among benthic amphipods with different lifestyles in a sandy surf zone of Korea. Crustaceana, 82 (11), 1441-1456. https://doi.org/10.1163/001121609X12511103974376
  • Zintzen, V., Massin, C., Norro, A. & Mallefet, J. (2006) Epifaunal inventory of two shipwrecks from the Belgian Continental Shelf. Hydrobiologia, 555, 207-219. https://doi.org/10.1007/s10750-005-1117-1
  • Zintzen, V., Norro, A., Massin, C. & Mallefet, J. (2008) Temporal variation of Tubularia indivis a (Cnidaria, Tubulariidae) and associated epizoites on artificial habitat communities in the North Sea. Marine Biology, 153, 405-420. https://doi.org/10.1007/s00227-007-0819-5