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dc.contributor.authorStachnik, Lukasz
dc.contributor.authorHawkings, Jonathan Robert
dc.contributor.authorSpolaor, Andrea
dc.contributor.authorStachniak, Katarzyna
dc.contributor.authorIgnatiuk, Dariusz
dc.contributor.authorSitek, Sławomir
dc.contributor.authorJanik, Krzysztof
dc.contributor.authorŁepkowska, Elżbieta
dc.contributor.authorBurgay, Francois
dc.contributor.authorSyczewski, Marcin Daniel
dc.contributor.authorSegato, Delia
dc.contributor.authorForjanes, Pablo
dc.contributor.authorBenning, Liane G.
dc.date.accessioned2025-07-09T12:30:59Z
dc.date.available2025-07-09T12:30:59Z
dc.date.issued2025-06-16
dc.description.abstractRapid warming in polar and alpine areas is causing significant glacier mass loss and resulting in increasing freshwater delivery to the oceans. Recent research indicates that higher meltwater water runoff is likely to increase solute and sediment transport, which will include nutrients, to downstream environments. This enhanced delivery may drive a negative feedback effect on atmospheric CO<sub>2</sub> concentrations by stimulating primary production in fjords and near-coastal regions. Labile sediment-bound nutrient species constitute a high proportion of the total nutrient yield from glacierised catchments, but studies that investigate their source and behaviour are sparse. Here we determine sediment-bound and dissolved nutrient (Si, Fe, P) delivery from a polythermal glacier in SW Spitsbergen. Suspended sediment and dissolved samples were collected from subglacial outflows and a downstream site. Our results show high spatial variability in chemical weathering processes resulting in differences in sediment-bound nutrient concentration. Sulphide oxidation and carbonate dissolution appear more important in a channelised system underlain by rocks metamorphosed in green schist facies, and silicate mineral weathering appears more important in smaller subglacial outflows underlain by rocks undergone intense metamorphism in amphibolite facies. Sediments from the channelised outlet have two times higher content of sediment-bound highly reactive iron (∼0.29 % dry weight, hereafter d.w.) than the minor subglacial outflows. In contrast, sediment-bound amorphous silica (ASi) is almost double in the minor subglacial outflows compared to the channelised outlet (∼0.17 % d.w. vs ∼0.10 % d.w.). The yield of sediment-bound Fe and Si (2.3 and 1.3 10<sup>3</sup> kg km<sup>−2</sup> yr<sup>−1</sup>, respectively) was several times higher than the dissolved flux of those elements. Sediment-bound Fe yields were in the range of values noted previously for the Greenland Ice Sheet. Our data reinforces the critical role of sediment-bound nutrients on elemental cycling in glacierised basins of the high Arctic.en_US
dc.identifier.citationStachnik L, Hawkings JR, Spolaor A, Stachniak, Ignatiuk D, Sitek S, Janik, Łepkowska E, Burgay F, Syczewski, Segato, Forjanes, Benning LG. Controls of sediment-bound and dissolved nutrient transport from a glacierised metasedimentary catchment in the high Arctic. Chemical Geology. 2025;691en_US
dc.identifier.cristinIDFRIDAID 2392153
dc.identifier.doi10.1016/j.chemgeo.2025.122940
dc.identifier.issn0009-2541
dc.identifier.issn1872-6836
dc.identifier.urihttps://hdl.handle.net/10037/37494
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.journalChemical Geology
dc.relation.projectIDNational Science Foundation: 2232980en_US
dc.relation.projectIDEC/H2020: 101005611en_US
dc.relation.projectIDNorges forskningsråd: 332635en_US
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/101005611/Norway/Electron and X-ray microscopy Community for structural and chemical Imaging Techniques for Earth materials/EXCITE/en_US
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2025 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleControls of sediment-bound and dissolved nutrient transport from a glacierised metasedimentary catchment in the high Arcticen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)