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Dissolved major ions, Sr and 87Sr/86Sr of coastal lakes from Larsemann hills, East Antarctica: Solute sources and chemical weathering in a polar environment

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dc.contributor.author Nuruzzama, Mohammad en_US
dc.contributor.author Rahaman, Waliur en_US
dc.contributor.author TRIPATHY, GYANA RANJAN en_US
dc.contributor.author Mohan, Rahul en_US
dc.contributor.author Patil, Shramik en_US
dc.date.accessioned 2020-05-29T05:11:01Z
dc.date.available 2020-05-29T05:11:01Z
dc.date.issued 2020-05 en_US
dc.identifier.citation Hydrological Processes, 34(11), 2351-2364. en_US
dc.identifier.issn 1099-1085 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4634
dc.identifier.uri https://doi.org/10.1002/hyp.13734 en_US
dc.description.abstract Dissolved major ions, Sr concentrations and 87Sr/86Sr ratios of 10 coastal lakes from the Larsemann Hills, East Antarctica have been studied to constrain their solute sources, transport and glacial weathering patterns in their catchments. In absence of perennial river/streams, lakes serve as only reliable archive to study land surface processes in these low‐temperature regions. The lake water chemistry is mostly Na‐Cl type and it does not show any significant depth variations. Sr isotope compositions of these lakes vary from 0.7110 to 0.7211 with an average value of 0.7145, which is higher than modern seawater value. In addition to oceanic sources, major ions and Sr isotopic data show appreciable amount of solute supply from chemical weathering of silicate rocks in lake catchments and dissolution of Ca‐Mg rich salts produced during the freezing of seawaters. The role of sulphide oxidation and carbonate weathering are found to be minimal on lake hydro‐chemistry in this part of Antarctica. Inverse model calculations using this chemical dataset provide first‐order estimates of dissolved cations and Sr; they are mostly derived from oceanic (seawater + snow) sources (cations approximately 76%) and (Sr approximately 92%) with minimal supplies from weathering of silicates (cations approximately 15%); (Sr approximately 2%) and Ca‐rich minerals (cations approximately 9%); (Sr approximately 7%). The silicate weathering rate and its corresponding atmospheric CO2 consumption rate estimates for Scandrett lake catchment (3.6 ± 0.3 tons/km2/year and 0.5 × 105 moles/km2/year), are lower than that of reported values for the average global river basins (5.4 tons/km2/year and 0.9 × 105 tons/km2/year) respectively. The present study provides a comprehensive report of chemical weathering intensity and its role in atmospheric CO2 consumption in low‐temperature pristine environment of Antarctica. These estimates underscore the importance of Antarctica weathering on atmospheric CO2 budget, particularly during the past warmer periods when the large area was exposed and available for intense chemical weathering. en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Antarctica en_US
dc.subject Coastal lakes en_US
dc.subject Glacial weathering en_US
dc.subject Inverse model en_US
dc.subject Sr isotopes en_US
dc.subject Water chemistry en_US
dc.subject TOC-MAY-2020 en_US
dc.subject 2020 en_US
dc.subject 2020-MAY-WEEK4 en_US
dc.title Dissolved major ions, Sr and 87Sr/86Sr of coastal lakes from Larsemann hills, East Antarctica: Solute sources and chemical weathering in a polar environment en_US
dc.type Article en_US
dc.contributor.department Dept. of Earth and Climate Science en_US
dc.identifier.sourcetitle Hydrological Processes en_US
dc.publication.originofpublisher Foreign en_US


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