Sulfur redox chemistry governs diurnal antimony and arsenic cycles at Champagne Pool, Waiotapu, New Zealand

Champagne Pool, a sulfidic hot spring in New Zealand, exhibits distinct diurnal variations in antimony (Sb) and arsenic (As) concentrations, with daytime high and night-time low concentrations. To identify the underlying mobilization mechanisms, five sites along the drainage channel of Champagne Poo...

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Published inJournal of volcanology and geothermal research Vol. 262; pp. 164 - 177
Main Authors Ullrich, Maria K., Pope, James G., Seward, Terry M., Wilson, Nathaniel, Planer-Friedrich, Britta
Format Journal Article
LanguageEnglish
Published Oxford Elsevier B.V 15.07.2013
Elsevier
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Abstract Champagne Pool, a sulfidic hot spring in New Zealand, exhibits distinct diurnal variations in antimony (Sb) and arsenic (As) concentrations, with daytime high and night-time low concentrations. To identify the underlying mobilization mechanisms, five sites along the drainage channel of Champagne Pool were sampled every 2h during a 24h period. Temporal variations in elemental concentrations and Sb, As, and sulfur (S) speciation were monitored in the discharging fluid. Total trace element concentrations in filtered and unfiltered samples were analyzed using ICP-MS, and Sb, As and S species were determined by IC-ICP-MS. Sulfur speciation in the drainage channel was dominated by thiosulfate and sulfide at night, while sulfate dominated during the day. The distinct diurnal changes suggest that the transformations are caused by phototrophic sulfur-oxidizing bacteria. These bacteria metabolize thiosulfate and sulfide in daylight to form sulfate and, as suggested by modeling with PhreeqC, elemental sulfur. Sulfide consumption during the day results in undersaturation of antimony sulfides, which triggers the additional release of dissolved Sb. For As, diurnal cycles were much more pronounced in speciation than in total concentrations, with di- and trithioarsenate forming at night due to excess sulfide, and monothioarsenate forming from arsenite and elemental sulfur during the day. Sulfur speciation was thus found to control Sb and As in terms of both solubility and speciation. •We present detailed sulfur speciation data for Champagne Pool over a 24hcycle.•Sulfur speciation is subject to daylight dependent transformations.•Sulfide oxidation and thiosulfate disproportionation increase during the day.•Diurnal cycles in sulfur speciation control the equilibrium of stibnite dissolution.•Formation of thioarsenates is governed by diurnal cycles in sulfur species.
AbstractList Champagne Pool, a sulfidic hot spring in New Zealand, exhibits distinct diurnal variations in antimony (Sb) and arsenic (As) concentrations, with daytime high and night-time low concentrations. To identify the underlying mobilization mechanisms, five sites along the drainage channel of Champagne Pool were sampled every 2h during a 24h period. Temporal variations in elemental concentrations and Sb, As, and sulfur (S) speciation were monitored in the discharging fluid. Total trace element concentrations in filtered and unfiltered samples were analyzed using ICP-MS, and Sb, As and S species were determined by IC-ICP-MS. Sulfur speciation in the drainage channel was dominated by thiosulfate and sulfide at night, while sulfate dominated during the day. The distinct diurnal changes suggest that the transformations are caused by phototrophic sulfur-oxidizing bacteria. These bacteria metabolize thiosulfate and sulfide in daylight to form sulfate and, as suggested by modeling with PhreeqC, elemental sulfur. Sulfide consumption during the day results in undersaturation of antimony sulfides, which triggers the additional release of dissolved Sb. For As, diurnal cycles were much more pronounced in speciation than in total concentrations, with di- and trithioarsenate forming at night due to excess sulfide, and monothioarsenate forming from arsenite and elemental sulfur during the day. Sulfur speciation was thus found to control Sb and As in terms of both solubility and speciation. •We present detailed sulfur speciation data for Champagne Pool over a 24hcycle.•Sulfur speciation is subject to daylight dependent transformations.•Sulfide oxidation and thiosulfate disproportionation increase during the day.•Diurnal cycles in sulfur speciation control the equilibrium of stibnite dissolution.•Formation of thioarsenates is governed by diurnal cycles in sulfur species.
Champagne Pool, a sulfidic hot spring in New Zealand, exhibits distinct diurnal variations in antimony (Sb) and arsenic (As) concentrations, with daytime high and night-time low concentrations. To identify the underlying mobilization mechanisms, five sites along the drainage channel of Champagne Pool were sampled every 2 h during a 24 h period. Temporal variations in elemental concentrations and Sb, As, and sulfur (S) speciation were monitored in the discharging fluid. Total trace element concentrations in filtered and unfiltered samples were analyzed using ICP-MS, and Sb, As and S species were determined by IC-ICP-MS. Sulfur speciation in the drainage channel was dominated by thiosulfate and sulfide at night, while sulfate dominated during the day. The distinct diurnal changes suggest that the transformations are caused by phototrophic sulfur-oxidizing bacteria. These bacteria metabolize thiosulfate and sulfide in daylight to form sulfate and, as suggested by modeling with PhreeqC, elemental sulfur. Sulfide consumption during the day results in undersaturation of antimony sulfides, which triggers the additional release of dissolved Sb. For As, diurnal cycles were much more pronounced in speciation than in total concentrations, with di- and trithioarsenate forming at night due to excess sulfide, and monothioarsenate forming from arsenite and elemental sulfur during the day. Sulfur speciation was thus found to control Sb and As in terms of both solubility and speciation.
Author Wilson, Nathaniel
Seward, Terry M.
Planer-Friedrich, Britta
Ullrich, Maria K.
Pope, James G.
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  surname: Ullrich
  fullname: Ullrich, Maria K.
  email: maria.ullrich@uni-bayreuth.dec
  organization: University of Bayreuth, Environmental Geochemistry Group, Germany
– sequence: 2
  givenname: James G.
  surname: Pope
  fullname: Pope, James G.
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  fullname: Seward, Terry M.
  organization: Victoria University of Wellington, Volcanology, Geochemistry and Petrology Research Group, New Zealand
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  givenname: Nathaniel
  surname: Wilson
  fullname: Wilson, Nathaniel
  organization: University of Bayreuth, Environmental Geochemistry Group, Germany
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  givenname: Britta
  surname: Planer-Friedrich
  fullname: Planer-Friedrich, Britta
  organization: University of Bayreuth, Environmental Geochemistry Group, Germany
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Keywords As and Sb speciation
Diurnal variations
Elemental sulfur globules
Thioarsenates
time variations
bacteria
mobilization
Australasia
cycles
sulfates
diurnal variations
trace-element analyses
hot springs
arsenites
sulfides
antimony
concentration
consumption
arsenic
speciation
prokaryotes
channels
transformations
solubility
drainage
inductively coupled plasma
Language English
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Snippet Champagne Pool, a sulfidic hot spring in New Zealand, exhibits distinct diurnal variations in antimony (Sb) and arsenic (As) concentrations, with daytime high...
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SubjectTerms Antimony
As and Sb speciation
Bacteria
Champagne
Crystalline rocks
Diurnal variations
Earth sciences
Earth, ocean, space
Elemental sulfur globules
Exact sciences and technology
Igneous and metamorphic rocks petrology, volcanic processes, magmas
Pools
Speciation
Sulfates
Sulfides
Sulfur
Thioarsenates
Title Sulfur redox chemistry governs diurnal antimony and arsenic cycles at Champagne Pool, Waiotapu, New Zealand
URI https://dx.doi.org/10.1016/j.jvolgeores.2013.07.007
https://www.proquest.com/docview/1500785701
https://www.proquest.com/docview/1808127035
Volume 262
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