Monitoreo de contaminación por tributilestaño (TBT) en puertos de Paracas, Ica (Perú), mediante el fenómeno de Imposex en Stramonita chocolata
DOI:
https://doi.org/10.21142/cient.v12i3.328Keywords:
Imposex, Organoestañosos, Tributilestaño, S. chocolataAbstract
El imposex es la imposición de caracteres sexuales masculinos sobre el sistema reproductivo femenino de caracoles gasterópodos prosobranquios. Este fenómeno se ha asociado a compuestos organoestañosos empleados como
agentes biocidas en las pinturas antiincrustantes aplicadas sobre muelles, embarcaciones e instalaciones de cultivo,
principalmente con el tributilestaño (TBT). El presente trabajo pretende evaluar la ocurrencia de imposex en los caracoles
marinos Stramonita chocolata que habitan en la playa La Mina de la isla San Gallán (Ica, Perú). El porcentaje de imposex
fue del 33,3 %. El índice de la longitud relativa del pene (RPLI) fue de 36,23. La relación entre la longitud de la conchilla y
la longitud del pene en machos y en hembras no fue estadísticamente significativa.
Downloads
References
Almeida E, Diamantino T, De Sousa O. Marine paints: The particular case of antifouling paints. Progress in Organic Coatings. 2007; 59: 2-20.
Chacón O, Cuevas F, De La Fuente C, Díaz F, Huaquín L. Disrupción endocrina e imposex. Avances en Ciencias Veterinarias 2007; 22: 42-8.
Axiak V, Micallef D, Muscat J, Vella A, Mintoff B. Imposex as a biomonitoring tool for marine pollution by tributyltin: Some further observations. Environment International 2003; 28: 743-9.
Guzmán M, Ramírez P. Disfunción endocrina debido a contaminantes ambientales. Elementos 2012; 87: 19-25.
Gravel P, Johanning K, McLachlan J, Vargas J, Oberdörster E. Imposex in the intertidal snail Thais brevidentata (Gastropoda-Muricidae) from the Pacific coast of Costa Rica. Rev. Biol. Trop. 2006; 54: 21-6.
Oberdörster E, McClellan-Green P. The neuropeptide APGWamide induces imposex in the mud snail, Ilyanassa obsoleta. Peptides 2000; 21: 1323-30.
Oberdörster E, Romano J, McClellan-Green P. The Neuropeptide APGWamide as a Penis Morphogenic Factor (PMF) in Gastropod Mollusks. Integr. Comp. Biol. 2005; 45 (1): 28-32.
Gooding M, Gallardo C, Leblanc G. Imposex in three marine gastropod species in Chile and potential impact on mariciculture. Marine Pollution Bulletin 1999; 38: 1227-31.
LeBlanc G, Gooding M, Sternberg R. Testosterone-Fatty acid esterification: a unique target for the endocrine toxicity of tributyltin to gastropods. Integr. Comp. Biol. 2005; 45 (1): 81-7.
Matthiesen P, Gibbs P. Critical appraisal of the evidence for tributyltin-mediated endocrine disruption in mollusks. Environ. Toxicol. Chem. 1998; 17: 37-43.
McAllister B, Kime D. Early life exposure to environmental levels of the aromatase inhibitor tributyltin causes masculinization and irreversible sperm damage in zebrafish (Daniorerio). Aquat. Toxicol. 2003; 65: 309-16.
Gibbs P, Pascoe P, Burt G. Sex change in the female dogwhelks Nucella lapillus, induced by tributyltin from antifouling paints. Journal of the Marine Biological Association of the United Kingdom 1988; 68: 715-31.
Oehlmann J, Bettin C. Tributyltin- induced imposex and the role of steroids in marine snails. Malacol. Rev. Suppl. 1996; 6: 157-61.
Rodríguez F. Imposex en la laguna de Términos, Campeche, México. Revista Científica UDO Agrícola 2010; 10: 141-9.
Castro I, Perina F, Fillmann G. Organotin contamination in South American coastal areas. Environmental Monitoring and Assessment 2011; 184: 1781-99.
Kotrikla A. Environmental management aspects for TBT antifouling wastes from the shipyards. Journal of Environmental Management 2009; 90: 77-85.
Bryan G, Gibbs P, Pascoe P, Burt G. 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 1987; 67: 507-23.
Stroben E, Oehlmann J, Fioroni P. Hinia reticulata and Nucella lapillus. Comparison of two gastropod tributyltin bioindicators. Marine Biology 1992; 114: 289-96.
Barreiro R, Quintela M, Ruiz JM. TBT e imposex en Galicia: los efectos de un disruptor endocrino en poblaciones de gasterópodos marinos. Ecosistemas 2004; 13: 13-29.
Rodríguez J, Tueros I, Borja A, Franco J, Ignacio G, Garmendia J, Muxica I, Sariego C, Valencia V. European ports and along coastal areas. Continental Shelf Research 2008; 29: 1165-73.
De Mora S. The tributyltin debate: ocean transportation versus seafood harvesting. In: De Mora SJ (ed.). Tributyltin: case of study of an environmental contaminant. Cambridge: Cambridge University Press; 1996.
Fent K. Ecotoxicology of organotin compounds. Crit. Rev. Toxicol. 1996; 26: 1-117.
Champ M. A review of organotin regulatory strategies, pending actions, related costs and benefits. Sci. Total Environ. 2000; 258: 21-71.
Golub M, Doherty J. Triphenyltin as a potential human endocrine disruptor. Journal Toxicol. Environ. 2004; 7: 281-95.
Smith B. Tributyltin compounds induce male characteristics on female mud snails Nassarius obsoletus = Ilyanassa obsoleta. Journal Appl. Toxicol. 1981; 1: 141-4.
Smith B. The estuarine mud snail, Nassarius obsoletus: abnormalities in the reproductive system. Journal Mollus. Stud. 1980; 46: 247-56.
Bryan G, Burt G, Gibbs P, Pascoe P. 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 1993; 73: 913-29.
Horiguchi T, Shiraishi H, Shimizu M, Morita M. Imposex in sea snails, caused by organotin (tributyltin and triphenyltin) pollution in Japan: a survey. Appl. Organomet. Chem. 1997; 11: 451-5.
Nishikawa J. Imposex in marine gastropods may be caused by binding of organotins to retinoid X receptor. Mar. Biol. 2006; 149: 117-24.
Oehlmann J, Di Benedetto P, Tillman M, Duft M, Oetken M, Shulte-Oehlmann U. Endocrine disruption in prosobranch mollusks: evidence and ecological relevance. Ecotoxicology 2007; 16: 29-43.
Tittley-O´Neal C, MacDonald B, Pelletier E, Saint-Louis R, Phillips O. The relationship between imposex and Tributyltin (TBT) concentration in Strombus gigas from the British Virgin islands. Bulletin of Marine Science 2011; 87: 421-35.
Ramírez R, Paredes C, Arenas J. Moluscos del Perú. Revista de Biología Tropical 2003; 51: 225-89.
Castro I, Fillman G. High tribultyltin and imposex levels in the comercial muricid Thais chocolata from two Peruvian harbor areas. Environmental Toxicology and Chemistry 2012; 31: 1-6.
Miloslavich P, Penchaszadeh P, Bigatti G. Imposex en gastrópodos de Venezuela. Ciencias Marinas 2007; 33: 319-24.
Guabloche A, Álvarez J, Rivas R, Hurtado S, Pradel R, Iannacone J. Imposex in the marine snail Xanthochorus buxea (Broderip, 1833) (Muricidae) from the South American Pacific. The Biologist 2013; 11 (2): 237-49.
Vasconcelos P, Moura P, Barroso C, Gaspar M. Size matters: Importance of penis length variation on reproduction studies and imposex monitoring in Bolinus brandaris. Hydrobiologia 2011; 661: 363-75.
Bezerra F, Braga I, De Almeida C. Imposex occurrence in Nassarius vibex from South America: a potential bioindicator in estuarine environments. Marine Biodiversity Records 2010; 3.
Caetano C, Albsalao R. Imposex in Olivancillaria vesica (Gmelin) (Gastropoda,Olividae) from Southeastern Brazilian Sandy beach. Revista Brasileira de Zoologia 2002; 19: 215-18.
Morcillo Y, Porte C. Monitoring of organotin compounds and their effects in marine molluscs. Trends Anal. Chem. 1998; 17: 109-16.
Kure L, Depledge M. Accumulation of organotin in Littorina littorea and Mya arenaria from Danish coastal waters. Environ. Pollut. 1994; 84: 149-57.
Downloads
Published
Issue
Section
License
Este obra está bajo una licencia de Creative Commons Reconocimiento-NoComercial-CompartirIgual 4.0 Internacional.