Synergies in elemental mobility during weathering of tetrahedrite [(Cu,Fe,Zn)<sub>12</sub>(Sb,As)<sub>4</sub>S<sub>13</sub>]: Field observations, electron microscopy, isotopes of Cu, C, O, radiometric dating, and water geochemistry

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Authors

  • J. Majzlan
  • S. Kiefer
  • Julia Hermann
  • M. Števko
  • J. Sejkora
  • M. Chovan
  • T. Lánczos
  • M. Lazarov
  • A. Gerdes
  • F. Langenhorst
  • A. Borčinová Radková
  • H. Jamieson
  • R. Milovský

Research Organisations

External Research Organisations

  • Goethe University Frankfurt
  • Friedrich Schiller University Jena
  • National Museum Prague
  • Comenius University
  • Queen's University Kingston
  • Slovak Academy of Sciences
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Details

Original languageEnglish
Pages (from-to)1-20
Number of pages20
JournalChemical geology
Volume488
Publication statusPublished - 5 Jun 2018

Abstract

Tetrahedrite [(Cu,Fe,Zn) 12(Sb,As) 4S 13] is commonly present in many ore deposits and may be transferred to mining waste. Here, we describe the behavior of all elements in tetrahedrite during oxidative dissolution in a natural oxidation zone at Piesky (Slovakia), this being a long-term analogue of weathering of tetrahedrite-rich mining wastes. Electron microprobe work identified initial, early, advanced, and mature stages of weathering. The initial stages include formation of secondary covellite and chalcocite, the following stages only oxidic products, divided into greenish masses and brown veinlets. Both of them are nanocrystalline mixtures of minerals. The masses are Cu-Sb-As-rich and consist of a nanocrystalline pyrochlore phase. The veinlets are Fe-Sb-As rich and contain tripuhyite, goethite, and pyrochlores. Quantitative elemental budgets show that some elements (Zn, S, Ni, Co) are rapidly lost whereas others (especially Cu and As) are retained and form copper arsenates in the mature stages of weathering. About 10% As and almost 50% of Sb are lost during weathering, likely released into water; some Sb is stored in secondary minerals such as camérolaite, cualstibite, or tripuhyite. Light carbon isotopic composition (δ 13C down to −11.1‰) document significant biological contribution for C in the secondary minerals. Copper isotopes become progressively heavier during weathering (from initial δ 65Cu of −2.45‰ in tetrahedrite up to 4.3‰ in some azurite samples but −6.3‰ in covellite and chalcocite), documenting cyclic removal of light copper isotopes into covellite and chalcocite. The observation of elemental synergies during weathering of tetrahedrite shows that the solubility and mobility of As is controlled by copper arsenates, not by iron oxides, in an environment rich in tetrahedrite but poor in pyrite. Antimony, another element of environmental concern, is mostly released into water and creates low-concentration anomalies in stream sediments and soils.

Keywords

    Carbon, oxygen, copper isotopes, Electron microprobe, Radiometric dating, Stibiconite, Tetrahedrite, Tripuhyite, Water geochemistry, Weathering

ASJC Scopus subject areas

Cite this

Synergies in elemental mobility during weathering of tetrahedrite [(Cu,Fe,Zn)<sub>12</sub>(Sb,As)<sub>4</sub>S<sub>13</sub>]: Field observations, electron microscopy, isotopes of Cu, C, O, radiometric dating, and water geochemistry. / Majzlan, J.; Kiefer, S.; Hermann, Julia et al.
In: Chemical geology, Vol. 488, 05.06.2018, p. 1-20.

Research output: Contribution to journalArticleResearchpeer review

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title = "Synergies in elemental mobility during weathering of tetrahedrite [(Cu,Fe,Zn)12(Sb,As)4S13]: Field observations, electron microscopy, isotopes of Cu, C, O, radiometric dating, and water geochemistry",
abstract = "Tetrahedrite [(Cu,Fe,Zn) 12(Sb,As) 4S 13] is commonly present in many ore deposits and may be transferred to mining waste. Here, we describe the behavior of all elements in tetrahedrite during oxidative dissolution in a natural oxidation zone at Piesky (Slovakia), this being a long-term analogue of weathering of tetrahedrite-rich mining wastes. Electron microprobe work identified initial, early, advanced, and mature stages of weathering. The initial stages include formation of secondary covellite and chalcocite, the following stages only oxidic products, divided into greenish masses and brown veinlets. Both of them are nanocrystalline mixtures of minerals. The masses are Cu-Sb-As-rich and consist of a nanocrystalline pyrochlore phase. The veinlets are Fe-Sb-As rich and contain tripuhyite, goethite, and pyrochlores. Quantitative elemental budgets show that some elements (Zn, S, Ni, Co) are rapidly lost whereas others (especially Cu and As) are retained and form copper arsenates in the mature stages of weathering. About 10% As and almost 50% of Sb are lost during weathering, likely released into water; some Sb is stored in secondary minerals such as cam{\'e}rolaite, cualstibite, or tripuhyite. Light carbon isotopic composition (δ 13C down to −11.1‰) document significant biological contribution for C in the secondary minerals. Copper isotopes become progressively heavier during weathering (from initial δ 65Cu of −2.45‰ in tetrahedrite up to 4.3‰ in some azurite samples but −6.3‰ in covellite and chalcocite), documenting cyclic removal of light copper isotopes into covellite and chalcocite. The observation of elemental synergies during weathering of tetrahedrite shows that the solubility and mobility of As is controlled by copper arsenates, not by iron oxides, in an environment rich in tetrahedrite but poor in pyrite. Antimony, another element of environmental concern, is mostly released into water and creates low-concentration anomalies in stream sediments and soils.",
keywords = "Carbon, oxygen, copper isotopes, Electron microprobe, Radiometric dating, Stibiconite, Tetrahedrite, Tripuhyite, Water geochemistry, Weathering",
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year = "2018",
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TY - JOUR

T1 - Synergies in elemental mobility during weathering of tetrahedrite [(Cu,Fe,Zn)12(Sb,As)4S13]: Field observations, electron microscopy, isotopes of Cu, C, O, radiometric dating, and water geochemistry

AU - Majzlan, J.

AU - Kiefer, S.

AU - Hermann, Julia

AU - Števko, M.

AU - Sejkora, J.

AU - Chovan, M.

AU - Lánczos, T.

AU - Lazarov, M.

AU - Gerdes, A.

AU - Langenhorst, F.

AU - Borčinová Radková, A.

AU - Jamieson, H.

AU - Milovský, R.

N1 - Publisher Copyright: © 2018 Elsevier B.V.

PY - 2018/6/5

Y1 - 2018/6/5

N2 - Tetrahedrite [(Cu,Fe,Zn) 12(Sb,As) 4S 13] is commonly present in many ore deposits and may be transferred to mining waste. Here, we describe the behavior of all elements in tetrahedrite during oxidative dissolution in a natural oxidation zone at Piesky (Slovakia), this being a long-term analogue of weathering of tetrahedrite-rich mining wastes. Electron microprobe work identified initial, early, advanced, and mature stages of weathering. The initial stages include formation of secondary covellite and chalcocite, the following stages only oxidic products, divided into greenish masses and brown veinlets. Both of them are nanocrystalline mixtures of minerals. The masses are Cu-Sb-As-rich and consist of a nanocrystalline pyrochlore phase. The veinlets are Fe-Sb-As rich and contain tripuhyite, goethite, and pyrochlores. Quantitative elemental budgets show that some elements (Zn, S, Ni, Co) are rapidly lost whereas others (especially Cu and As) are retained and form copper arsenates in the mature stages of weathering. About 10% As and almost 50% of Sb are lost during weathering, likely released into water; some Sb is stored in secondary minerals such as camérolaite, cualstibite, or tripuhyite. Light carbon isotopic composition (δ 13C down to −11.1‰) document significant biological contribution for C in the secondary minerals. Copper isotopes become progressively heavier during weathering (from initial δ 65Cu of −2.45‰ in tetrahedrite up to 4.3‰ in some azurite samples but −6.3‰ in covellite and chalcocite), documenting cyclic removal of light copper isotopes into covellite and chalcocite. The observation of elemental synergies during weathering of tetrahedrite shows that the solubility and mobility of As is controlled by copper arsenates, not by iron oxides, in an environment rich in tetrahedrite but poor in pyrite. Antimony, another element of environmental concern, is mostly released into water and creates low-concentration anomalies in stream sediments and soils.

AB - Tetrahedrite [(Cu,Fe,Zn) 12(Sb,As) 4S 13] is commonly present in many ore deposits and may be transferred to mining waste. Here, we describe the behavior of all elements in tetrahedrite during oxidative dissolution in a natural oxidation zone at Piesky (Slovakia), this being a long-term analogue of weathering of tetrahedrite-rich mining wastes. Electron microprobe work identified initial, early, advanced, and mature stages of weathering. The initial stages include formation of secondary covellite and chalcocite, the following stages only oxidic products, divided into greenish masses and brown veinlets. Both of them are nanocrystalline mixtures of minerals. The masses are Cu-Sb-As-rich and consist of a nanocrystalline pyrochlore phase. The veinlets are Fe-Sb-As rich and contain tripuhyite, goethite, and pyrochlores. Quantitative elemental budgets show that some elements (Zn, S, Ni, Co) are rapidly lost whereas others (especially Cu and As) are retained and form copper arsenates in the mature stages of weathering. About 10% As and almost 50% of Sb are lost during weathering, likely released into water; some Sb is stored in secondary minerals such as camérolaite, cualstibite, or tripuhyite. Light carbon isotopic composition (δ 13C down to −11.1‰) document significant biological contribution for C in the secondary minerals. Copper isotopes become progressively heavier during weathering (from initial δ 65Cu of −2.45‰ in tetrahedrite up to 4.3‰ in some azurite samples but −6.3‰ in covellite and chalcocite), documenting cyclic removal of light copper isotopes into covellite and chalcocite. The observation of elemental synergies during weathering of tetrahedrite shows that the solubility and mobility of As is controlled by copper arsenates, not by iron oxides, in an environment rich in tetrahedrite but poor in pyrite. Antimony, another element of environmental concern, is mostly released into water and creates low-concentration anomalies in stream sediments and soils.

KW - Carbon, oxygen, copper isotopes

KW - Electron microprobe

KW - Radiometric dating

KW - Stibiconite

KW - Tetrahedrite

KW - Tripuhyite

KW - Water geochemistry

KW - Weathering

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U2 - 10.1016/j.chemgeo.2018.04.021

DO - 10.1016/j.chemgeo.2018.04.021

M3 - Article

VL - 488

SP - 1

EP - 20

JO - Chemical geology

JF - Chemical geology

SN - 0009-2541

ER -

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