2007
DOI: 10.1016/j.marenvres.2007.03.001
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Stramonita haemastoma as a bioindicator for organotin contamination in coastal environments

Abstract: Stramonita haemastoma was investigated as a suitable bioindicator of TBT and TPhT contamination in the tropical Atlantic Ocean by: 1. Imposex induction in healthy females after inoculation with TBT and TPhT in the laboratory; and 2. Determining incidence of imposex in S. haemastoma collected from areas with various levels of tributyltin (TBT) and triphenyltin (TPhT) and determining the concentrations of these chemical in its tissues and that of its prey, the mussell Perna pernas. Imposex intensities and organo… Show more

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Cited by 48 publications
(23 citation statements)
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References 44 publications
(63 reference statements)
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“…It can accumulate more in animals at lower trophic levels because they have a poor capacity to degrade this compound. 33 The results of this study can be compared with those obtained by Limaverde et al 20 using the gastropod Stramonita haemastoma and the bivalve Perna perna as bioindicators, with TBT concentrations ranging from < LOD to 62 ng Sn g -1 (155 ng TBT g -1 ) for S. haemastoma and < LOD to 110 ng Sn g -1 (275 ng TBT g -1 ) for P. perna. For crustaceans, Takeuchi et al 30 quantified TBT in amphipods (Caprella spp.)…”
Section: Application Of the Methodsmentioning
confidence: 68%
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“…It can accumulate more in animals at lower trophic levels because they have a poor capacity to degrade this compound. 33 The results of this study can be compared with those obtained by Limaverde et al 20 using the gastropod Stramonita haemastoma and the bivalve Perna perna as bioindicators, with TBT concentrations ranging from < LOD to 62 ng Sn g -1 (155 ng TBT g -1 ) for S. haemastoma and < LOD to 110 ng Sn g -1 (275 ng TBT g -1 ) for P. perna. For crustaceans, Takeuchi et al 30 quantified TBT in amphipods (Caprella spp.)…”
Section: Application Of the Methodsmentioning
confidence: 68%
“…The tissue extraction is a modification of the proposed method by Limaverde et al 20 for organotin extractions in mussel tissue. The extraction was performed by adding 3.5 mL of hydrochloric acid and 5 mL of methanol, homogenizing in vortex for 1 min for digestion.…”
Section: Butyltin Extractionmentioning
confidence: 99%
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