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Differences in organochlorine accumulation accompanying life history in the catadromous eel Anguilla japonica and the marine eel Conger myriaster

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Abstract

In order to examine the ecological risk for organic pollutants in diadromous fish migrating between sea and freshwater, organochlorine compounds (OCs) were determined in the catadromous eel Anguilla japonica having marine, estuarine and freshwater residence life histories. The eels were collected in Japanese coastal areas. We also compared the OCs accumulation with the marine eel Conger myriaster, which has a similar life history as A. japonica in the marine environment. The ontogenic changes in the otolith strontium (Sr) and calcium (Ca) concentrations were examined along the life history transect to discriminate the migration type. There were generally three different patterns, which were categorized as ‘marine residence’ (spent most of their life in the sea and did not enter freshwater), ‘estuarine residence’ (inhabited estuaries or switched between different habitats), and ‘freshwater residence’ (entered and remained in freshwater river habitats after arrival in the estuary) according to the otolith Sr:Ca ratio. There were generally no correlations between OCs such as Dichlorodiphenyltrichloroethanes (DDTs), Hexachlorobenzene (HCB), Hexachlorocyclohexanes (HCHs) and Chlordanes (CHLs) accumulation and each biological characteristic such as TL, BW and age in A. japonica. A positive correlation between the lipid content and concentrations of OCs were found. Additionally, the concentrations of HCB, ∑HCHs, ∑CHLs and ∑DDTs in A. japonica were significantly higher than those of C. myriaster, associating with the higher lipid contents (14% on average) in the former than the latter eels (9% on average). A negative linear relationship was found between the otolith Sr:Ca ratios and concentration of each OCs in A. japonica. The ecological risk of OCs increase as the freshwater residence period in the eel becomes longer. It is clear that migratory histories and lipid contents directly affected OCs accumulation in the anguillid eels.

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References

  • Albaigfs J, Farran A, Soler M, Gallifa A (1987) Accumulation and distribution of biogenic and pollutant hydrocarbons, PCBs and DDTs in tissues of western Mediterranean fish. Mar Environ Res 22:1–18

    Article  Google Scholar 

  • Arai T, Otake T, Tsukamoto K (1997) Drastic changes in otolith microstructure and microchemistry accompanying the onset of metamorphosis in the Japanese eel Anguilla japonica. Mar Ecol Prog Ser 161:17–22

    Article  CAS  Google Scholar 

  • Arai T, Kotake A, Lokman PM, Miller MJ, Tsukamoto K (2004) Evidence of different habitat use by New Zealand freshwater eels Anguilla australis and A. dieffenbachii, as revealed by otolith microchemistry. Mar Ecol Prog Ser 266:213–225

    Article  Google Scholar 

  • Arai T, Kotake A, McCarthy TK (2006) Habitat use by the European eel Anguilla anguilla in Irish waters. Estuar Coast Shelf Sci 67:569–578

    Article  Google Scholar 

  • Bidleman TF, Wall MD, Roura R, Carr E, Schmidt S (1993) Organochlorine pesticides in the atmosphere of the Southern Ocean and Antarctica, January–March, 1990. Mar Pollut Bull 26:258–262

    Article  CAS  Google Scholar 

  • Boetius I, Boetius J (1980) Experimental maturation of female silver eels, Anguilla Anguilla estimated of fecundity and energy reserves for migration and spawning. Dana 1:1–28

    Google Scholar 

  • Chino N, Arai T (2009) Relative contribution of migratory type on the reproduction of migrating silver eels, Anguilla japonica, collected off Shikoku Island, Japan. Mar Biol 156:661–668

    Article  CAS  Google Scholar 

  • Chino N, Arai T (2010a) Migratory history of the giant mottled eel Anguilla marmorata in the Bonin Islands of Japan. Ecol Freshw Fish 19:19–25

    Article  Google Scholar 

  • Chino N, Arai T (2010b) Occurrence of marine resident tropical eel Anguilla bicolor bicolor in Indonesia. Mar Biol 157:1075–1081

    Article  Google Scholar 

  • Chino N, Arai T (2010c) Habitat use and habitat transitions in the tropical eel, Anguilla bicolor bicolor. Environ Biol Fish 89:571–578

    Article  Google Scholar 

  • Chiuchiolo AL, Dickhut RM, Cochran MA, Ducklow HW (2004) Pesticides organic pollutants at the base of the Antarctic marine food web. Environ Sci Technol 38:3551–3557

    Article  CAS  Google Scholar 

  • Colborn T, Smolen MJ (1996) Epidemiological analysis of persistent organochlorine contaminants in cetaceans. Rev Environ Contam Toxicol 146:91–172

    Article  CAS  Google Scholar 

  • Corsi I, Mariottini M, Badesso A, Caruso T, Borghesi N, Bonacci S, Iacocca A, Focardi S (2005) Contamination and sub-lethal toxicological effects of persistent organic pollutants in the European eel (Anguilla anguilla) in the Orbetello lagoon (Tuscany, Italy). Hydrobiologia 550:237–249

    Article  CAS  Google Scholar 

  • De Boer J, Dao QT, van Leeuwen SPJ, Kotterman MJJ, Schobben JHM (2010) Thirty year monitoring of PCBs, organochlorine pesticides and tetrabromodiphenylether in eel from The Netherlands. Environ Pollut 158:1228–1236

    Article  Google Scholar 

  • de Brito APX, Ueno D, Takahashi S, Tanabe S (2002) Organochlorine and butyltin residues in walleye Pollock (Theragra chalcogramma) from Bering Sea, Gulf of Alaska and Japan Sea. Chemosphere 46:401–411

    Article  Google Scholar 

  • De Silva SS, Gunasekera RM, Collins RO (2002) Some morphometric and biochemical features of ready-to-migrate silver and pre-migratory yellow stages of the shortfin eel of south-eastern Australian waters. J Fish Biol 61:915–928

    Article  Google Scholar 

  • Ewald GP, Larsson H, Linge L, Okla L, Szarzi N (1998) Biotransport of organic pollutants to an inland Alaska lake by migrating sockeye salmon (Onchorhynchus nerka). Arctic 51:40–47

    Google Scholar 

  • Ferrante MC, Clausi MT, Meli R, Fusco G, Naccari C, Lucisano A (2010) Polychlorinated biphenyls and organochlorine pesticides in European eel (Anguilla anguilla) from the Garigliano River (Campania region, Italy). Chemosphere 78:709–716

    Article  CAS  Google Scholar 

  • Fisk AT, Tittlemier SA, Pranschke JL, Norstrom RJ (2002) Using anthropogenic contaminants and stable isotopes to assess the feeding ecology of Greenland shark. Ecology 83:2162–2172

    Article  Google Scholar 

  • Fu S, Chu S, Xu X (2001) Organochlorine pesticide residue in soils from Tibet, China. Bull Environ Contam Toxicol 66:171–177

    Article  CAS  Google Scholar 

  • Hamilton MC, Hites RA, Schwager SJ, Foran JA, Knuth BA, Carpenter DO (2005) Lipid composition and contaminations in farmed and wild salmon. Environ Sci Technol 39:8622–8629

    Article  CAS  Google Scholar 

  • Iwata H, Tanabe S, Sakai N, Tatsukawa R (1993) Distribution of persistent organochlorines in the oceanic air and surface seawater and the role of ocean on their global transport and fate. Environ Sci Technol 27:1080–1098

    Article  CAS  Google Scholar 

  • Knights B (1997) Risk assessment and management of contamination of eels (Anguilla spp.) by persistent xenobiotic organochlorine compounds. Chem Ecol 13:171–212

    Article  CAS  Google Scholar 

  • Krümmel EM, MacDonald RW, Kimpe LE, Gregory-Eaves I, Demers MJ, Smol JP, Finney B, Blais JM (2003) Delivery of pollutants by spawning salmon. Nature 425:255–256

    Article  Google Scholar 

  • Larsson P, Hamrin S, Okla L (1991) Factors determining the uptake of persistent pollutants in a eel population (Anguilla anguilla L.). Environ Pollut 69:39–50

    Article  CAS  Google Scholar 

  • Lokman PM, Vermeulen G, Lambert JGD, Young G (1998) Gonad histology and plasma steroid profiles in wild New Zealand freshwater eels (Anguilla dieffenbachii and A. australis) before and at the onset of the natural spawning migration. I. Females. Fish Physiol Biochem 19:325–338

    Article  CAS  Google Scholar 

  • Lum KR, Kaiser KLE, Comba ME (1987) Export of mirex from Lake Ontario to the St. Lawrence estuary. Sci Total Environ 67:41–51

    Article  CAS  Google Scholar 

  • Maes J, Goemans G, Belpaire C (2008) Spatial variation and temporal pollution profiles of polychlorinated biphenyls, organochlorine pesticides and heavy metals in European yellow eel (Anguilla anguilla L.) (Flanders, Belgium). Environ Pollut 153:223–237

    Article  CAS  Google Scholar 

  • Matsui I (1972) Eel biology-biological study. Koseisha-Koseikaku, Tokyo

    Google Scholar 

  • McHugh B, Poole R, Corcoran J, Anninou P, Boyle B, Joyce E, Foley MB, McGovern E (2010) The occurrence of persistent chlorinated and brominated organic contaminants in the European eel (Anguilla anguilla) in Irish waters. Chemosphere 79:305–313

    Article  CAS  Google Scholar 

  • Merna JW (1986) Contamination of stream fishes with chlorinated hydrocarbons from eggs to Great Lakes salmon. Trans Am Fish Soc 115:69–74

    Article  CAS  Google Scholar 

  • Monirith I, Nakata H, Tanabe S, Tana TS (1999) Persistent organochlorine residues in marine and freshwater fish in Cambodia. Mar Pollut Bull 38:604–612

    Article  CAS  Google Scholar 

  • Naiman RJ, Bilby RE, Schindler DE, Helfield JM (2002) Pacific salmon, nutrients, and the dynamics of freshwater and riparian ecosystems. Ecosystems 5:399–417

    Article  Google Scholar 

  • Naismith IA, Knights B (1990) Modelling of unexploited and exploited populations of Anguilla anguilla (L.), in the Thames Estuary. J Fish Biol 37:975–986

    Article  Google Scholar 

  • Niimi AJ, Oliver BG (1983) Biological half-lives of plychlorinated biphenyls (PCB) congeners in whole fish and muscle of rainbow trout (Salmo gardner). Can J Fish Aquat Sci 40:1388–1394

    Article  CAS  Google Scholar 

  • Pastor D, Boix J, Fernandez V, Albaiges J (1996) Bioaccumulation of organochlorinated contaminants in three estuarine fish species (Mullus barbatus, Mugil cephalus and Dicentrarcus labrax). Mar Pollut Bull 32:257–262

    Article  CAS  Google Scholar 

  • Pizza JC, O’Connor JM (1983) PCB dynamics in Hudson River striped bass. II Accumulation from dietary sources. Aquat Toxicol 3:313–327

    Article  CAS  Google Scholar 

  • Rossel D, Honsberger P, Tarradellas J (1987) Bioaccumulative behaviour of some PCB congeners in lake Geneva Brown Trout (Salmo trutta laccustris L.). Int J Environ Anal Chem 31:219–233

    Article  CAS  Google Scholar 

  • Scrudato RJ, McDowell WH (1989) Upstream transport of mirex by migrating salmonids. Can J Fish Aquat Sci 46:1484–1488

    Article  Google Scholar 

  • Sokal RR, Rohlf FJ (1995) Biometry. The principles and practice of statistics in biological research, 3rd edn. WH Freeman and Company, New York

    Google Scholar 

  • Spigarelli SA, Thommes MM, Prepejchal W (1983) Thermal and metabolic factors affecting PCB uptake by adult brown trout. Environ Sci Technol 17:88–94

    Article  CAS  Google Scholar 

  • Szlinder-Richert J, Usydus Z, Pelczarski W (2010) Organochlorine pollutants in European eel (Anguilla anguilla L.) from Poland. Chemosphere 80:93–99

    Article  CAS  Google Scholar 

  • Takai T (1959) Studies on the morphology, ecology and culture of the important apodal fishes, Muraenesox cinereus (Forsskal) and Conger myriaster (Brevoort). J Shimonoseki Coll Fish 8:209–555

    Google Scholar 

  • Tesch FW (1977) The eel. Biology and management of anguillid eels. Chapman & Hall, London

    Google Scholar 

  • Tulonen J, Vuorinen PJ (1996) Concentrations of PCBs and other organochlorine compounds in eels (Anguilla anguilla L.) of the Vanajavesi watercourse in southern Finland, 1990–1993. Sci Total Environ 187:11–18

    Article  CAS  Google Scholar 

  • Utoh T, Mikawa N, Okamura A, Yamada Y, Tanaka S, Horie N, Akazawa A, Oka HP (2004) Ovarian morphology of the Japanese eel in Mikawa Bay. J Fish Biol 64:502–513

    Article  Google Scholar 

  • Van der Oost R, Opperhuizen A, Satumalay K, Heida H, Vermeulen NPE (1996) Biomonitoring aquatic pollution with feral eel (Anguilla anguilla). 1. Bioaccumulation: biota-sediment ratios of PCBs, OCPs, PCDDs and PCDFs. Aquat Toxicol 35:21–46

    Article  Google Scholar 

  • Wania F, Mackay D (1996) Tracking the distribution of persistent organic pollutants. Environ Sci Technol 30:390–396

    Article  Google Scholar 

Download references

Acknowledgment

This work was supported in part by Grant-in-Aid No. 20688008 from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.

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Authors and Affiliations

  1. International Coastal Research Center, Ocean Research Institute, The University of Tokyo, 2-106-1, Akahama, Otsuchi, Iwate, 028-1103, Japan

    Takaomi Arai

  2. Department of Biology, Faculty of Science, Universiti Putra Malaysia, 43400, UPM Serdang, Selangor, Malaysia

    Takaomi Arai

  3. School of Fisheries Sciences, Kitasato University, 160-4, Sanriku, Ofunato, Iwate, 022-0101, Japan

    Akina Takeda

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  1. Takaomi Arai
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Correspondence to Takaomi Arai.

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Arai, T., Takeda, A. Differences in organochlorine accumulation accompanying life history in the catadromous eel Anguilla japonica and the marine eel Conger myriaster . Ecotoxicology 21, 1260–1271 (2012). https://doi.org/10.1007/s10646-012-0881-8

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