Organically bound iodine as a bottom-water redox proxy : preliminary validation and application

dc.contributor.author Zhou, Xiaoli
dc.contributor.author Jenkyns, Hugh C.
dc.contributor.author Lu, Wanyi
dc.contributor.author Hardisty, Dalton S.
dc.contributor.author Owens, Jeremy D.
dc.contributor.author Lyons, Timothy W.
dc.contributor.author Lu, Zunli
dc.date.accessioned 2017-07-17T14:40:06Z
dc.date.issued 2017-03-15
dc.description © The Author(s), 2017. This is the author's version of the work. It is posted here under a nonexclusive, irrevocable, paid-up, worldwide license granted to WHOI. It is made available for personal use, not for redistribution. The definitive version was published in Chemical Geology 457 (2017): 95-106, doi:10.1016/j.chemgeo.2017.03.016. en_US
dc.description.abstract Carbonate-associated iodine (I/Ca) has been used as a proxy of local, upper-ocean redox conditions, and has successfully demonstrated highly dynamic spatial and temporal patterns across different time scales of Earth history. To further explore the utility of iodine as a paleo-environmental proxy, we present here a new method of extracting organically bound iodine (Iorg) from shale using volumes of samples on the order of tens of milligrams, thus offering the potential for high-resolution work across thin shale beds. The ratio of Iorg to total organic carbon (I/TOC) in modern surface and subsurface sediments decreases with decreasing bottom-water oxygen, which may be used to reconstruct paleo-redox changes. As a proof of concept, we evaluate the I/TOC proxy in Holocene sediments from the Baltic Sea, Landsort Deep (IODP 347) and discuss those data within a framework of additional independent redox proxies, e.g., iron speciation and [Mo]. The results imply that I/TOC may be sensitive to hypoxic–suboxic conditions, complementary to proxies sensitive to more reducing, anoxic–euxinic conditions. Then, we test the usage of I/TOC in sediments deposited during Late Cretaceous, Cenomanian–Turonian Oceanic Anoxic Event (OAE) 2 from ~ 94 million years ago (Ma). We generated I/TOC and Iorg records from six OAE 2 sections: Tarfaya (Morocco), Furlo (central Italy), Demerara Rise (western equatorial Atlantic), Cape Verde Basin (eastern equatorial Atlantic), South Ferriby (UK), and Kerguelen Plateau (southern Indian Ocean), which provide a broad spatial coverage. Generally, I/TOC decreases over the interval recorded by the positive carbon-isotope excursion, the global signature of OAE 2, suggesting an expansion of more reducing bottom-water conditions and consistent with independent constraints from iron speciation and redox-sensitive trace-metals (e.g., Mo). Relatively higher I/TOC values (thus more oxic conditions) are recorded at two high latitude sites for OAE 2, supporting previous model simulations (cGENIE) that indicated higher bottom water oxygen concentrations in these regions. Our results also indicate that organic-rich and oxygenated seafloors are likely a major sink of iodine and correspondingly influence its global seawater inventory. en_US
dc.description.sponsorship XZ, WL and ZL are supported by NSF EAR 1349252. DH and TWL acknowledge support from the Geobiology and Low-temperature Geochemistry (GG) Program of NSF. DH would like to acknowledge a Schlanger Ocean Drilling Fellowship. en_US
dc.identifier.uri https://hdl.handle.net/1912/9105
dc.language.iso en_US en_US
dc.relation.uri https://doi.org/10.1016/j.chemgeo.2017.03.016
dc.subject I/TOC en_US
dc.subject Bottom water en_US
dc.subject OAE 2 en_US
dc.subject Black shale en_US
dc.subject Baltic en_US
dc.title Organically bound iodine as a bottom-water redox proxy : preliminary validation and application en_US
dc.type Preprint en_US
dspace.entity.type Publication
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