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dc.contributor.authorNuruzzama, Mohammaden_US
dc.contributor.authorRahaman, Waliuren_US
dc.contributor.authorTRIPATHY, GYANA RANJANen_US
dc.contributor.authorMohan, Rahulen_US
dc.contributor.authorPatil, Shramiken_US
dc.date.accessioned2020-05-29T05:11:01Z-
dc.date.available2020-05-29T05:11:01Z-
dc.date.issued2020-05en_US
dc.identifier.citationHydrological Processes, 34(11), 2351-2364.en_US
dc.identifier.issn1099-1085en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4634-
dc.identifier.urihttps://doi.org/10.1002/hyp.13734en_US
dc.description.abstractDissolved 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.isoenen_US
dc.publisherWileyen_US
dc.subjectAntarcticaen_US
dc.subjectCoastal lakesen_US
dc.subjectGlacial weatheringen_US
dc.subjectInverse modelen_US
dc.subjectSr isotopesen_US
dc.subjectWater chemistryen_US
dc.subjectTOC-MAY-2020en_US
dc.subject2020en_US
dc.subject2020-MAY-WEEK4en_US
dc.titleDissolved major ions, Sr and 87Sr/86Sr of coastal lakes from Larsemann hills, East Antarctica: Solute sources and chemical weathering in a polar environmenten_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Earth and Climate Scienceen_US
dc.identifier.sourcetitleHydrological Processesen_US
dc.publication.originofpublisherForeignen_US
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