Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-13T07:15:24.184Z Has data issue: false hasContentIssue false

Ecological plasticity of the European eel Anguilla anguilla in a tidal Atlantic lake system in Ireland

Published online by Cambridge University Press:  07 February 2019

Takaomi Arai*
Affiliation:
Environmental and Life Sciences Programme, Faculty of Science, Universiti Brunei Darussalam, Jalan Tungku Link, Gadong, BE 1410, Brunei Darussalam
Aya Kotake
Affiliation:
Atmosphere and Ocean Research Institute, The University of Tokyo 5-1-5, Kashiwanoha, Kashiwa, Chiba 277-8564, Japan
Chris Harrod
Affiliation:
Department of Zoology, National University of Ireland, Galway, University Road, Galway, Ireland Instituto de Ciencias Naturales Alexander Von Humboldt, Universidad de Antofagasta, Avenida Angamos 601, Antofagasta, Chile
Michelle Morrissey
Affiliation:
Department of Zoology, National University of Ireland, Galway, University Road, Galway, Ireland
T. Kieran McCarthy
Affiliation:
Department of Zoology, National University of Ireland, Galway, University Road, Galway, Ireland
*
Author for correspondence: Takaomi Arai, E-mail: takaomi.arai@ubd.edu.bn

Abstract

Recent studies have shown that anguillid eel populations in habitats spanning the marine–freshwater ecotone can display extreme plasticity in the range of catadromy expressed by individual fish. The apparent use of marine and freshwater habitats by the European eel Anguilla anguilla was examined by analysing the strontium (Sr) and calcium (Ca) concentrations in otoliths of eels collected from a tidal Atlantic lake system in Ireland. Variations of the Sr:Ca ratio in the otoliths indicated that a variety of environmental salinities had been experienced in the habitats that were occupied during the growth phase of these individuals in the tidal Atlantic lake system. The otolith microchemistry of these eels indicated that most of the eels had entered each salinity environment (freshwater (FW); brackish water (BW); marine-dominated water (MW) and full seawater (SW)) from fresh water to full seawater just after recruitment and had stayed in each environment until maturation without movement to other salinity environments. Only 2 of 93 (2%) eels had shifted their habitat once in their lives. This result suggests that each individual might have an environmental habitat preference, although each individual could move along a short (<2 km) salinity gradient.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2019 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Arai, T and Chino, N (2012) Diverse migration strategy between freshwater and seawater habitats in the freshwater eels genus Anguilla. Journal of Fish Biology 81, 442455.Google Scholar
Arai, T and Chino, N (2017) Influence of water salinity on the strontium:calcium ratios in otoliths of the giant mottled eel, Anguilla marmorata. Environmental Biology of Fishes 100, 281286.Google Scholar
Arai, T, Otake, T and Tsukamoto, K (2000) Timing of metamorphosis and larval segregation of the Atlantic eels, Anguilla rostrata and A. anguilla, as revealed by otolith microstructure and microchemistry. Marine Biology 137, 3945.Google Scholar
Arai, T, Kotake, A, Ohji, M, Miller, MJ, Tsukamoto, K and Miyazaki, N (2003 a) Occurrence of sea eels of Anguilla japonica along the Sanriku Coast of Japan. Ichthyological Research 50, 7881.Google Scholar
Arai, T, Kotake, A, Ohji, M, Miyazaki, N and Tsukamoto, K (2003 b) Migratory history and habitat use of Japanese eel Anguilla japonica in the Sanriku Coast of Japan. Fisheries Science 69, 813818.Google Scholar
Arai, T, Kotake, A, Lokman, PM, Miller, MJ and Tsukamoto, K (2004) Evidence of different habitat use by New Zealand freshwater eels, Anguilla australis and A. dieffenbachii, as revealed by otolith microchemistry. Marine Ecology Progress Series 266, 213225.Google Scholar
Arai, T, Kotake, A and McCarthy, TK (2006) Habitat use by the European eel Anguilla anguilla in Irish waters. Estuarine Coastal and Shelf Science 67, 569578.Google Scholar
Arkhipkin, AI, Schuchert, PC and Danyushevsky, L (2009) Otolith chemistry reveals fine population structure and close affinity to the Pacific and Atlantic oceanic spawning grounds in the migratory southern blue whiting (Micromesistius australis australis). Fisheries Research 96, 188194.Google Scholar
Berkes, F and Seixas, CS (2005) Building resilience in lagoon social-ecological systems: a local-level perspective. Ecosystems 8, 967974.Google Scholar
Bertin, L (1956) Eels – A Biological Study. London: Cleaver-Hume Press.Google Scholar
Blaber, SJM, Young, JW and Dunning, MC (1985) Community structure and zoogeographic affinities of the coastal fishes of Dampier region of north-western Australia. Australian Journal of Marine and Freshwater Research 36, 247266.Google Scholar
Boëtius, J (1985) Greenland eels. Anguilla rostrata Lesueur. Dana 4, 4148.Google Scholar
Bozeman, EK, Helfman, GS and Richardson, T (1985) Population size and home range of American eels in a Georgia tidal creek. Transaction of American Fisheries Society 114, 821825.Google Scholar
Burnet, AMR (1969) The growth of New Zealand freshwater eels in three Canterbury streams. New Zealand Journal of Marine and Freshwater Research 3, 376384.Google Scholar
Campana, SE (1999) Chemistry and composition of fish otoliths: pathways, mechanisms and applications. Marine Ecology Progress Series 188, 263297.Google Scholar
Casselman, JM (2003) Dynamics of resources of the American eel, Anguilla rostrata: declining abundance in the 1990s. In Aida, K, Tsukamoto, K and Yamauchi, K (eds), Eel Biology. Tokyo: Springer-Verlag, pp. 255274.Google Scholar
Chisnall, BL and Hicks, BJ (1993) Age and growth of longfinned eels (Anguilla dieffenbachii) in pastoral and forested streams in the Waikato River basin, and in two hydroelectric lakes in the North Island. New Zealand Journal of Marine and Freshwater Research 27, 317332.Google Scholar
Dekker, W, Casselman, JM, Cairns, DK, Tsukamoto, K, Jellyman, D and Lickers, H (2003) Worldwide decline of eel resources necessitates immediate action: Québec Declaration of Concern. Fisheries 28, 2830.Google Scholar
Elsdon, TS and Gillanders, BM (2002) Interactive effects of temperature and salinity on otolith chemistry: challenges for determining environmental histories of fish. Canadian Journal of Fisheries and Aquatic Science 59, 17961808.Google Scholar
Fernandez-Delgado, C, Hernando, JA, Herrera, M and Bellido, M (1989) Age and growth of yellow eels, Anguilla anguilla, in the estuary of the Guadalquiver River (south-west Spain). Journal of Fish Biology 34, 561570.Google Scholar
Ford, TE and Mercer, E (1986) Density, size distribution and home range of American eels, Anguilla rostrata, in a Massachusetts salt marsh. Environmental Biology of Fishes 17, 309314.Google Scholar
Frost, PC, Tank, SE, Turner, MA and Elser, JJ (2003) Elemental composition of littoral invertebrates from oligotrophic and eutrophic Canadian lakes. Journal of the North American Benthological Society 22, 5162.Google Scholar
Gross, MR (1987) The evolution of diadromy fishes. American Fisheries Society Symposium 1, 1425.Google Scholar
Gross, MR, Coleman, RM and McDowall, RM (1988) Aquatic productivity and the evolution of diadromous fish migration. Science 239, 12911293.Google Scholar
Harrod, C, Grey, J, McCarthy, TK and Morrissey, M (2005) Stable isotope analyses provide new insights into ecological plasticity in a mixohaline population of European eel. Oecologia 144, 673683.Google Scholar
Jellyman, DJ and Sykes, JRE (2003) Diel and seasonal movements of radio-tagged freshwater eels, Anguilla spp., in two New Zealand streams. Environmental Biology of Fishes 66, 143154.Google Scholar
Kennish, MJ and Paerl, HW (2010) Coastal Lagoons: Critical Habitats of Environmental Change. Boca Raton, FL: CRC Press.Google Scholar
Kjerve, B (ed.) (1990) Coastal lagoons. In Coastal Lagoon Processes, Elsevier Oceanographic Series 60. Amsterdam: Elsevier, pp. 18.Google Scholar
Kotake, A, Arai, T, Ozawa, T, Nojima, S, Miller, MJ and Tsukamoto, K (2003) Variation in migratory history of Japanese eels, Anguilla japonica, collected in coastal waters of the Amakusa Islands, Japan, inferred from otolith Sr/Ca ratios. Marine Biology 142, 849854.Google Scholar
Kotake, A, Okamura, A, Yamada, Y, Utoh, T, Arai, T, Miller, MJ, Oka, HP and Tsukamoto, K (2005) Seasonal variation in migratory history of the Japanese eel, Anguilla japonica, in Mikawa Bay, Japan. Marine Ecology Progress Series 293, 213221.Google Scholar
Kraus, RT and Secor, DH (2004) Incorporation of strontium into otoliths of an estuarine fish. Journal of Experimental Marine Biology and Ecology 302, 85106.Google Scholar
Lamson, H, Shiao, JC, Iizuka, Y, Tzeng, WN and Cairns, DK (2006) Movement patterns of American eels (Anguilla rostrata) between salt- and freshwater in a coastal watershed, based on otolith microchemistry. Marine Biology 149, 15671576.Google Scholar
Lenanton, TCJ (1982) Alternative non-estuarine nursery habitats for some commercially and recreationally important fish species of south-western Australia. Australian Journal of Marine and Freshwater Research 33, 881900.Google Scholar
Lin, SH, Chang, CW, Iizuka, Y and Tzeng, WN (2007) Salinities, not diets, affect strontium/calcium ratios in otoliths of Anguilla japonica. Journal of Experimental Marine Biology and Ecology 34, 254263.Google Scholar
Lin, YJ, Yalçin-Özdilek, S, Iizuka, Y, Gümüş, A and Tzeng, WN (2011) Migratory life history of European eel Anguilla anguilla from freshwater regions of the River Asi, southern Turkey and their high otolith Sr:Ca ratios. Journal of Fish Biology 78, 860868.Google Scholar
Martin, GB, Thorrold, SR and Jones, CM (2004) Temperature and salinity effects on strontium incorporation in otoliths of larval spot (Leiostomus xanthurus). Canadian Journal of Fisheries and Aquatic Science 61, 3442.Google Scholar
McCarthy, TK, Cullen, P and O'Connor, W (1999) The biology and management of River Shannon eel populations. Fishery Bulletin (Dublin) 17, 920.Google Scholar
Moriarty, C (1996) The European eel fishery in 1993 and 1994. Fishery Bulletin (Dublin) 14, 152.Google Scholar
Munro, AR, McMahon, TE and Ruzycki, JR (2005) Natural chemical markers identify source and date of introduction of an exotic species: lake trout (Salvelinus namaycush) in Yellowstone Lake. Canadian Journal of Fisheries and Aquatic Science 62, 7987.Google Scholar
Oliveira, K (1997) Movement and growth rates of yellow phase American eels in the Annaquatucket River, Rhode Island. Transactions of American Fisheries Society 126, 638646.Google Scholar
Pankhurst, NW (1982) Relation of visual changes to the onset of sexual maturation in the European eel Anguilla anguilla (L.). Journal of Fish Biology 21, 127140.Google Scholar
Parker, SJ (1995) Homing ability and home-range of yellow-phase American eels in a tidally dominated estuary. Journal of the Marine Biological Association of the United Kingdom 75, 127140.Google Scholar
Penczak, T (1985) Phosphorus, nitrogen and carbon cycling by fish populations in two small lowland rivers in Poland. Hydrobiologia 120, 159165.Google Scholar
Poole, WR (1990) Summer fyke nets as a method of eel capture in a salmonid fishery. Aquaculture and Fisheries Management 21, 259262.Google Scholar
Salonen, K, Sarvala, J, Hakala, I and Viljanen, ML (1976) The relation of energy and organic carbon in aquatic invertebrates. Limnology and Oceanography 21, 724730.Google Scholar
Schmidt, J (1922) The breeding places of the eel. Philosophical Transactions of Royal Society of London B 211, 179208.Google Scholar
Schmidt, J (1925) The breeding places of the eel. Smithsonian Institute Annual Report 1924, 279316.Google Scholar
Schuchert, PC, Arkhipkin, AI and Koenig, AE (2010) Traveling around Cape Horn: otolith chemistry reveals a mixed stock of Patagonian hoki with separate Atlantic and Pacific spawning grounds. Fisheries Research 102, 8086.Google Scholar
Shiao, JC, Ložys, L, Iizuka, Y and Tzeng, WN (2006) Migratory patterns and contribution of stocking to the population of European eel in Lithuanian waters as indicated by otolith Sr:Ca ratios. Journal of Fish Biology 69, 749769.Google Scholar
Sokal, RR and Rohlf, FJ (1995) Biometry: The Principles and Practice of Statistics in Biological Research, 3rd Edn. New York, NY: WH Freeman.Google Scholar
Tabouret, H, Bareille, G, Claverie, F, Pécheyran, C, Prouzet, P and Donard, OFX (2010) Simultaneous use of strontium:calcium and barium:calcium ratios in otoliths as markers of habitat: application to the European eel (Anguilla anguilla) in the Adour basin, South West France. Marine Environmental Research 70, 3545.Google Scholar
Tanner, DK, Brazner, JC and Brady, VJ (2000) Factors influencing carbon, nitrogen, and phosphorus content of fish from a Lake Superior coastal wetland. Canadian Journal of Fisheries and Aquatic Science 57, 12431251.Google Scholar
Tesch, FW (2003) The Eel, 5th Edn. Oxford: Blackwell Publishing.Google Scholar
Tsukamoto, K and Arai, T (2001) Facultative catadromy of the eel, Anguilla japonica, between freshwater and seawater habitats. Marine Ecology Progress Series 220, 265276.Google Scholar
Tzeng, WN (1996) Effects of salinity and ontogenetic movements on strontium:calcium ratios in the otoliths of the Japanese eel, Anguilla japonica Temminck and Schlegel. Journal of Experimental Marine Biology and Ecology 199, 111122.Google Scholar
Tzeng, WN, Iizuka, Y, Shiao, JC, Yamada, Y and Oka, HP (2003) Identification and growth rates comparison of divergent migratory contingents of Japanese eel (Anguilla japonica). Aquaculture 216, 7786.Google Scholar
Wang, CH and Tzeng, WN (2000) The timing of metamorphosis and growth rates of American and European eel leptocephali: a mechanism of larval segregative migration. Fisheries Research 46, 191205.Google Scholar