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dc.contributor.authorMartínez Ruiz, Francisca
dc.contributor.authorGonzález Muñoz, María Teresa 
dc.contributor.authorJroundi, Fadwa 
dc.contributor.authorAbad Ortega, María del Mar 
dc.date.accessioned2020-05-22T07:05:40Z
dc.date.available2020-05-22T07:05:40Z
dc.date.issued2018-10-06
dc.identifier.citationF. Martinez-Ruiz, et al. Barite formation in the ocean: Origin of amorphous and crystalline precipitates. Chemical Geology 511 (2019) 441–451 [https://doi.org/10.1016/j.chemgeo.2018.09.011]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/62181
dc.descriptionWe also thank editors and two anonymous reviewers for helpful comments that have significantly improved this contribution.es_ES
dc.description.abstractOcean export production is a key constituent in the global carbon cycle impacting climate. Past ocean export production is commonly estimated by means of barite and Barium proxies. However, the precise mechanisms underlying barite precipitation in the undersaturated marine water column are not fully understood. Here we present a detailed mineralogical and crystallographic analysis of barite from size-fractionated particulate material collected using multiple unit large volume in-situ filtration systems in the North Atlantic and the Southern Ocean. Our data suggest that marine barite forms from an initial amorphous phosphorus-rich phase that binds Ba, which evolves into barite crystals whereby phosphate groups are substituted by sulfate. Scanning electron microscopy observations also show the association of barite particles with organic matter aggregates and with extracellular polymeric substances (EPS). These results are consistent with experimental work showing that in bacterial biofilms Ba binds to phosphate groups in both cells and EPS, which promotes locally high concentrations of Ba leading to saturated microenvironments favoring barite precipitation. These results strongly suggest a similar precipitation mechanism in the ocean, which is consistent with the close link between bacterial production and abundance of Ba-rich particulates in the water column. We argue that EPS play a major role in mediating barite formation in the undersaturated oceanic water column; specifically, increased productivity and organic matter degradation in the mesopelagic zone would entail more extensive EPS production, thereby promoting Ba bioaccumulation and appropriate microenvironments for barite precipitation. This observation contributes toward better understanding of Ba proxies and their utility for reconstructing past ocean export productivity. This article is part of a special issue entitled: “Cycles of trace elements and isotopes in the ocean – GEOTRACES and beyond” - edited by Tim M. Conway, Tristan Horner, Yves Plancherel, and Aridane G. González.es_ES
dc.description.sponsorshipThis study was supported by the European Regional Development Fund (ERDF) co-financed grants CGL2015-66830-R and CGL2017- 92600-EXP (MINECO Secretaría de Estado de Investigación, Desarrollo e Innovación, Spain), Research Group RNM-179 and BIO 103 (Consejería de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía) and the University of Granada (Unidad Científica de Excelencia UCE-PP2016-05). We thank the Center for Scientific Instrumentation (CIC, University of Granada), the Warm Core Rings project, and NSF OCE- 0961660 for supporting sample collection during MV1101.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectMarine baritees_ES
dc.subjectOcean productivityes_ES
dc.subjectBacteria es_ES
dc.subjectBiofilmses_ES
dc.subjectSustancias poliméricas extracelulares (EPS)es_ES
dc.subjectExtracellular polymeric substances (EPS)es_ES
dc.subjectBarite precipitationes_ES
dc.subjectMarine baritees_ES
dc.titleBarite formation in the ocean: Origin of amorphous and crystalline precipitateses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.1016/j.chemgeo.2018.09.011


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