Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-26T13:15:12.040Z Has data issue: false hasContentIssue false

Imposex occurrence in Nassarius vibex from South America: a potential bioindicator in estuarine environments

Published online by Cambridge University Press:  07 April 2010

Flávia Bezerra Lima-Verde*
Affiliation:
Laboratório de Zoobentos—Instituto de Ciências do Mar, Avenida da Abolição, 3207 Bairro Meireles, 60165-081, Fortaleza, CE, Brazil
Ítalo Braga de Castro
Affiliation:
Laboratório de Microcontaminantes Orgânicos e Ecotoxicologia Aquática—Fundação Universidade Federal do Rio Grande, CP 474, CEP 96201-900, Rio Grande, RS, Brazil
Cristina de Almeida Rocha-Barreira
Affiliation:
Laboratório de Zoobentos—Instituto de Ciências do Mar, Avenida da Abolição, 3207 Bairro Meireles, 60165-081, Fortaleza, CE, Brazil
*
Correspondence should be addressed to: F.B. Lima-Verde, Laboratório de Zoobentos—Instituto de Ciências do Mar, Avenida da Abolição, 3207 Bairro Meireles, 60165-081, Fortaleza, CE, Brazil email: [email protected]
Get access

Abstract

Research on organotin compounds (OTCs) contamination in South America is focused on sand/rocky environments; estuarine areas have not yet been investigated. Imposex is an important tool to evaluate OTC contamination. The aim of the present study was to assess the sensitivity of a typical estuarine species to OTC contamination and to biomonitor the spatial extent of such compounds in the estuary. Sampling was conducted along the Ceará River estuary (north-eastern Brazil) and imposex expression was quantified in Nassarius vibex females. Imposexed females developed small papillae or penis, with smaller lengths compared to males. Passive monitoring was conducted on 10 sampling stations around 2 shipyards using imposex quantification indices. Imposex percentage in the population ranged from 0 to 33.3% and relative penis length index ranged from 0 to 26.4%. The present research is the first application of N. vibex as a bioindicator of organotin compounds in Brazil.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2010

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

REFERENCES

Barreiro, R., Gonzáles, R., Quintela, M. and Ruiz, J.M. (2001) Imposex, organotin bioacumulation and sterility of female Nassarius reticulatus in polluted areas of NW Spain. Marine Ecology Progress Series 218, 203212.CrossRefGoogle Scholar
Barroso, C.M. and Moreira, M.H. (1998) Reproductive cycle of Nassarius reticulatus in the Ria de Aveiro, Portugal: implications for imposex studies. Journal of the Marine Biological Association of the United Kingdom 78, 12331246.CrossRefGoogle Scholar
Barroso, C.M., Moreira, M.H. and Bebianno, M.J. (2002a) Imposex, female sterility and organotin contamination of the prosobranch Nassarius reticulatus from the Portuguese coast. Marine Ecology Progress Series 230, 127135.Google Scholar
Barroso, C.M., Reis-Henriques, M.A., Ferreira, M.S. and Moreira, M.H. (2002b) The effectiveness of some compounds derived from antifouling paints in promoting imposex in Nassarius reticulatus. Journal of the Marine Biological Association of the United Kingdom 82, 249255.Google Scholar
Barroso, C.M., Moreira, M.H. and Richardson, C.A. (2005a) Age and growth of Nassarius reticulatus in Ria de Aveiro, north-west Portugal. Journal of the Marine Biological Association of the United Kingdom 85, 151156.CrossRefGoogle Scholar
Barroso, C.M., Reis-Henriques, M.A., Ferreira, M., Gibbs, P.E. and Moreira, M.H. (2005b) Organotin contamination, imposex and androgen/oestrogen ratios in natural populations of Nassarius reticulatus along a ship density gradient. Applied Organometallic Chemistry 19, 11411148.Google Scholar
Bigatti, G. and Penchaszadeh, P.E. (2005) Imposex in Odontocymbiola magellanica (Caenogastropoda: Volutidae) in Patagonia. Comunicaciones de la Sociedad Malacológica del Uruguay 88, 371375.Google Scholar
Bigatti, G., Primost, M., Cledón, M., Averbuj, A., Theobald, N., Gerwinski, W., Arntz, W., Morriconi, E. and Penchaszadeh, P. (2009) Biomonitoring of TBT contamination and imposex incidence along 4700 km of Argentinean shoreline (SW Atlantic: from 38S to 54S). Marine Pollution Bulletin 58, 695701.Google Scholar
Bryan, G.W., Burt, G.R., Gibbs, P.E. and Pascoe, P.L. (1993) Nassarius reticulatus (Nassariidae: Gastropoda) as an indicator of tributyltin pollution before and after TBT restrictions. Journal of the Marine Biological Association of the United Kingdom 73, 913929.Google Scholar
Cardoso, R.S., Caetano, C.H.S. and Cabrini, T.M.B. (2009) Biphallia in imposexed females of marine gastropods: new record for Nassarius vibex from Brazil. Brazilian Journal of Biology 69, 1, 223224.Google Scholar
Castro, I.B., Matthews-Cascon, H. and Fernandez, M.A. (2000) Imposex em Thais haemastoma (Linnaeus, 1767) (Mollusca: Gastropoda), uma indicação da contaminação por organoestânicos na costa do município de Fortaleza—Ceará—Brasil. Arquivos de Ciências do Mar 33, 5156.Google Scholar
Castro, I.B., Bemvenuti, C.E. and Fillmann, G. (2007a) Preliminary appraisal of imposex in areas under the influence of southern Brazilian harbors. Journal of the Brazilian Society of Ecotoxicology 2, 7379.CrossRefGoogle Scholar
Castro, I.B., Lima, A.F.A., Braga, A.R.C. and Rocha-Barreira, C.A. (2007b) Imposex in two muricid species (Mollusca: Gastropoda) from the northeastern Brazilian coast. Journal of the Brazilian Society of Ecotoxicology 2, 8191.Google Scholar
Chan, K. and Morton, B. (2003) The effects of organotin pollution on Nassarius festivus (Powys, 1835) (Gastropoda: Nassariidae) in Hong Kong. In Morton, B. (ed.) Proceedings of an International Workshop Reunion Conference, Hong Kong. Perspectives on Marine Environment Change in Hong Kong and Southern China, 1977–2001. Hong Kong: Hong Kong University Press, pp. 555578.Google Scholar
Coelho, J.P., Pimenta, J., Gomes, R., Barroso, C.M., Pereira, M.E., Pardal, M.A. and Duarte, A. (2006) Can Nassarius reticulatus be used as a bioindicator of Hg contamination? Results from a longitudinal study of the Portuguese coastline. Marine Pollution Bulletin 52, 674680.CrossRefGoogle ScholarPubMed
Demaintenon, M.J. (2001a) Analysis of reproductive system ontogeny and homology in Nassarius vibex (Gastropoda: Buccinidae: Nassariinae). Journal of Molluscan Studies 67, 3749.CrossRefGoogle Scholar
Demaintenon, M.J. (2001b) Ontogeny of the pseudohermafroditic reproductive system in Nassarius vibex (Gastropoda: Buccinidae: Nassariinae). Journal of Molluscan Studies 67, 5157.CrossRefGoogle Scholar
Fernandez, M.A., Wagener, A.D.L.R., Limaverde, A.M., Scofield, A.L., Pinheiro, F.M. and Rodrigues, E. (2005) Imposex and surface sediment speciation: a combined approach to evaluate organotin contamination in Guanabara Bay, Rio de Janeiro, Brazil. Marine Environmental Research 59, 435452.CrossRefGoogle ScholarPubMed
Gibbs, P.E., Bryan, G.W., Pascoe, P.L. & Burt, G.R. (1987) The use of the dog-whelk, Nucella lapillus, as an indicator of tributyltin (TBT) contamination. Journal of the Marine Biological Association of the United Kingdom 67, 507523.CrossRefGoogle Scholar
Gooding, M., Gallardo, C. and Leblanc, G. (1999) Imposex in three marine gastropod species in Chile and potential impact on mariculture. Marine Pollution Bulletin 38, 12271231.Google Scholar
Limaverde, A.M., Fernandez, M.A. and Coutinho, R. (2007) Stramonita haemastoma as a bioindicator for organotin contamination in coastal environments. Marine Environmental Research 64, 384398.CrossRefGoogle ScholarPubMed
Lima-Verde, F.B., Rocha-Barreira, C.A. and Castro, I.B. (2006) Caracterização do imposex em Nassarius vibex (Say, 1822) (Gastropoda, Nassariidae) no estuário do Rio Ceará, Fortaleza, Ceará. Proceedings of the XI Congresso Nordestino de Ecologia, 10–14 May 2006. Recife: Sociedade Nordestina de Ecologia. CD-ROM.Google Scholar
Marshall, D.J. and Rajkumar, A. (2003) Imposex in the indigenous Nassarius kraussianus (Mollusca: Neogastropoda). Marine Pollution Bulletin 46, 11501155.CrossRefGoogle ScholarPubMed
Matthews, H.R. (1968) Notas sobre a família Nassariidae no nordeste brasileiro (Mollusca: Gastropoda). Arquivo Da Estação Biológica Marinha Da Universidade Federal do Ceará 8, 141143.Google Scholar
Matthiessen, P. and Gibbs, P.E. (1998) Critical appraisal of the evidence for tributyltin-mediated endocrine disruption in mollusks. Environmental Toxicology and Chemistry 17, 3743.Google Scholar
Michaud, M.H. and Pelletier, E. (2006) Sources and fate of butyltins in the St Lawrence Estuary ecosystem. Chemosphere 64, 10741082.CrossRefGoogle Scholar
Pavoni, B., Centanni, E., Valcanover, S., Fasolato, M., Ceccato, S. and Tagliapietra, D. (2007) Imposex levels and concentrations of organotin compounds (TBT and its metabolites) in Nassarius nitidus from the Lagoon Venice. Marine Pollution Bulletin 55, 505511.Google Scholar
Penchaszadeh, P.E., Averbuj, A. and Cledón, M. (2001) Imposex in gastropods from Argentina (South-Western Atlantic). Marine Pollution Bulletin 42, 9, 790791.Google Scholar
Rato, M., Gaspar, M.B., Takahashi, S., Yano, S., Tanabe, S. and Barroso, C. (2008) Inshore/offshore gradients of imposex and organotin contamination in Nassarius reticulates (L.) along the Portuguese coast. Marine Pollution Bulletin 56, 13231331.CrossRefGoogle Scholar
Rios, E. (1994) Seashells of Brazil. 2nd edition. Rio Grande: Fundação Universidade do Rio Grande.Google Scholar
Shi, H.H., Huang, C.J., Zhu, X.S., Yu, X.J. and Xie, W.Y. (2005) Generalized system of imposex and reproductive failure in female gastropods of coastal waters of mainland China. Marine Ecology Progress Series 304, 179189.CrossRefGoogle Scholar
Smith, B.S. (1981) Tributyltin compounds induce male characteristics on female mud snails Nassarius obsoletus = Ilyanassa obsoleta. Journal of Applied Toxicology 1, 141144.Google Scholar
Sousa, A., Mendo, S. and Barroso, C. (2005) Imposex and organotin contamination in Nassarius reticulatus (L.) along the Portuguese coast. Applied Organometallic Chemistry 19, 315323.CrossRefGoogle Scholar