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Biosorption of thorium on the external shell surface of bivalve mollusks: The role of shell surface microtopography
- Source :
-
Chemosphere . Feb2012, Vol. 86 Issue 6, p680-683. 4p. - Publication Year :
- 2012
-
Abstract
- Abstract: External shell surface (ESS) of bivalve mollusks is known to adsorb various metals dissolved in ambient water in high concentration. It is hypothesized here that the surface microtopography of the thin organic coating layer, periostracum, or calcareous shell (if periostracum was destroyed) plays a major role in the adsorption of actinides on ESS. Thorium (natural alpha-emitter) was used in short-term biosorption experiment with shell fragments of five bivalve mollusks. After a 72h exposure to Th (∼6kBqL−1), thorium concentration was measured on ESS using laser ablation inductively coupled plasma mass spectrometry; the distribution and density of alpha tracks were subsequently visualized by α-track autoradiography. A trend in reduced Th concentrations on the ESS was observed depending upon the species tested: (group 1 ∼4000μgg−1) Chlamys islandica (M.), Mercenaria mercenaria (L.), Dreissena polymorpha (P.)>(group 2 ∼1200μgg−1) Crassostrea virginica (G.)≫(group 3 ∼150μgg−1) Mytilus edulis L. The microtopography of ESS was characterized by scanning electron microscopy revealing the high porosity of the calcareous surface of C. islandica and M. mercenaria, lamellate surface of periostracum in D. polymorpha, uneven but a weakly porous surface of periostracum of C. virginica, and a nearly smooth surface of the periostracum of M. edulis. This work has demonstrated, for the first time, the presence of a strong correlation between concentration of adsorbed Th and ESS microtopography, and the role of the periostracum in this process is discussed. [Copyright &y& Elsevier]
Details
- Language :
- English
- ISSN :
- 00456535
- Volume :
- 86
- Issue :
- 6
- Database :
- Academic Search Index
- Journal :
- Chemosphere
- Publication Type :
- Academic Journal
- Accession number :
- 71250606
- Full Text :
- https://doi.org/10.1016/j.chemosphere.2011.11.023