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Article: Trace lead impacts biomineralization pathways during bacterial iron reduction

TitleTrace lead impacts biomineralization pathways during bacterial iron reduction
Authors
KeywordsLead
Biomineralization
Dissimilatory Iron Reduction
Lead mobility
Issue Date2008
Citation
Chemical Geology, 2008, v. 249, n. 3-4, p. 282-293 How to Cite?
AbstractDissimilatory Iron Reduction (DIR) is often implicated in both the remobilization of trace metals from sediments, and in the sequestration of trace metals into secondary mineral products. However, the factors controlling the extent of dissolution versus solid-phase redistribution have been elusive. We have made the following observations after incubating pure and Pb-substituted Fe (hydr)oxides with Shewanella putrefaciens 200R over 1200 h: 1) Pb substitution at a molar ratio of Pb:Fe = 5.19 × 10- 4 inhibited Fe reduction; 2) the presence of Pb enhanced Fe dissolution and inhibited biologically induced magnetite formation; 3) Pb dissolved incongruently with Fe and accumulated to 190 nmol l- 1 in the aqueous phase; and 4) the residual solid-phase Pb was partitioned between an unresolved poorly reducible phase and weak acid extractable (surface sorbed or carbonate) phases. The presence of trace metals and Pb in soils and sediments could partially explain the apparent absence of magnetite in many Fe-reducing environments and its paucity in the sedimentary record. Organic matter degradation rates in Pb contaminated ecosystems may be reduced because of the inhibition of DIR by Pb. We assert that Pb should be largely immobile under Fe-reducing conditions due to its incorporation into refractory secondary minerals. © 2008 Elsevier B.V. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/269683
ISSN
2023 Impact Factor: 3.6
2023 SCImago Journal Rankings: 1.506
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSturm, Arne-
dc.contributor.authorCrowe, Sean A.-
dc.contributor.authorFowle, David A.-
dc.date.accessioned2019-04-30T01:49:17Z-
dc.date.available2019-04-30T01:49:17Z-
dc.date.issued2008-
dc.identifier.citationChemical Geology, 2008, v. 249, n. 3-4, p. 282-293-
dc.identifier.issn0009-2541-
dc.identifier.urihttp://hdl.handle.net/10722/269683-
dc.description.abstractDissimilatory Iron Reduction (DIR) is often implicated in both the remobilization of trace metals from sediments, and in the sequestration of trace metals into secondary mineral products. However, the factors controlling the extent of dissolution versus solid-phase redistribution have been elusive. We have made the following observations after incubating pure and Pb-substituted Fe (hydr)oxides with Shewanella putrefaciens 200R over 1200 h: 1) Pb substitution at a molar ratio of Pb:Fe = 5.19 × 10- 4 inhibited Fe reduction; 2) the presence of Pb enhanced Fe dissolution and inhibited biologically induced magnetite formation; 3) Pb dissolved incongruently with Fe and accumulated to 190 nmol l- 1 in the aqueous phase; and 4) the residual solid-phase Pb was partitioned between an unresolved poorly reducible phase and weak acid extractable (surface sorbed or carbonate) phases. The presence of trace metals and Pb in soils and sediments could partially explain the apparent absence of magnetite in many Fe-reducing environments and its paucity in the sedimentary record. Organic matter degradation rates in Pb contaminated ecosystems may be reduced because of the inhibition of DIR by Pb. We assert that Pb should be largely immobile under Fe-reducing conditions due to its incorporation into refractory secondary minerals. © 2008 Elsevier B.V. All rights reserved.-
dc.languageeng-
dc.relation.ispartofChemical Geology-
dc.subjectLead-
dc.subjectBiomineralization-
dc.subjectDissimilatory Iron Reduction-
dc.subjectLead mobility-
dc.titleTrace lead impacts biomineralization pathways during bacterial iron reduction-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.chemgeo.2008.01.017-
dc.identifier.scopuseid_2-s2.0-41349103605-
dc.identifier.volume249-
dc.identifier.issue3-4-
dc.identifier.spage282-
dc.identifier.epage293-
dc.identifier.isiWOS:000255720100004-
dc.identifier.issnl0009-2541-

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