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  • 1
    In: Geochemistry, geophysics, geosystems, Hoboken, NJ : Wiley, 2000, 9(2008), 10, 1525-2027
    In: volume:9
    In: year:2008
    In: number:10
    In: extent:18
    Type of Medium: Online Resource
    Pages: 18 , graph. Darst
    ISSN: 1525-2027
    Language: English
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  • 2
    Publication Date: 2022-05-25
    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 Earth and Planetary Science Letters 463 (2017): 159-170, doi:10.1016/j.epsl.2017.01.032.
    Description: The Proterozoic Eon hosted the emergence and initial recorded diversification of eukaryotes. Oxygen levels in the shallow marine settings critical to these events were lower than today’s, although how much lower is debated. Here, we use concentrations of iodate (the oxidized iodine species) in shallow-marine limestones and dolostones to generate the first comprehensive record of Proterozoic near-surface marine redox conditions. The iodine proxy is sensitive to both local oxygen availability and the relative proximity to anoxic waters. To assess the validity of our approach, Neogene-Quaternary carbonates are used to demonstrate that diagenesis most often decreases and is unlikely to increase carbonate-iodine contents. Despite the potential for diagenetic loss, maximum Proterozoic carbonate iodine levels are elevated relative to those of the Archean, particularly during the Lomagundi and Shuram carbon isotope excursions of the Paleo- and Neoproterozoic, respectively. For the Shuram anomaly, comparisons to Neogene-Quaternary carbonates suggest that diagenesis is not responsible for the observed iodine trends. The baseline low iodine levels in Proterozoic carbonates, relative to the Phanerozoic, are linked to a shallow oxic-anoxic interface. Oxygen concentrations in surface waters would have at least intermittently been above the threshold required to support eukaryotes. However, the diagnostically low iodine data from mid-Proterozoic shallow-water carbonates, relative to those of the bracketing time intervals, are consistent with a dynamic chemocline and anoxic waters that would have episodically mixed upward and laterally into the shallow oceans. This redox instability may have challenged early eukaryotic diversification and expansion, creating an evolutionary landscape unfavorable for the emergence of animals.
    Description: TL, ZL, and DH thank NSF EAR-1349252. ZL further thanks OCE-1232620. DH, ZL, and TL acknowledge further funding from a NASA Early Career Collaboration Award. TL, AB, NP, DH, and AK thank the NASA Astrobiology Institute. TL and NP received support from the Earth-Life Transitions Program of the NSF. AB acknowledges support from NSF grant EAR-05-45484 and an NSERC Discovery and Accelerator Grants. CW acknowledges support from NSFC grant 40972021.
    Keywords: Proterozoic oxygen ; Shuram isotope anomaly ; Carbonate diagenesis ; Bahamas ; Iodine ; Metazoan evolution
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 3
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2015. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography 30 (2015): 510–526, doi:10.1002/2014PA002741.
    Description: Global warming lowers the solubility of gases in the ocean and drives an enhanced hydrological cycle with increased nutrient loads delivered to the oceans, leading to increases in organic production, the degradation of which causes a further decrease in dissolved oxygen. In extreme cases in the geological past, this trajectory has led to catastrophic marine oxygen depletion during the so-called oceanic anoxic events (OAEs). How the water column oscillated between generally oxic conditions and local/global anoxia remains a challenging question, exacerbated by a lack of sensitive redox proxies, especially for the suboxic window. To address this problem, we use bulk carbonate I/Ca to reconstruct subtle redox changes in the upper ocean water column at seven sites recording the Cretaceous OAE 2. In general, I/Ca ratios were relatively low preceding and during the OAE interval, indicating deep suboxic or anoxic waters exchanging directly with near-surface waters. However, individual sites display a wide range of initial values and excursions in I/Ca through the OAE interval, reflecting the importance of local controls and suggesting a high spatial variability in redox state. Both I/Ca and an Earth System Model suggest that the northeast proto-Atlantic had notably higher oxygen levels in the upper water column than the rest of the North Atlantic, indicating that anoxia was not global during OAE 2 and that important regional differences in redox conditions existed. A lack of correlation with calcium, lithium, and carbon isotope records suggests that neither enhanced global weathering nor carbon burial was a dominant control on the I/Ca proxy during OAE 2.
    Description: Z.L. thanks NSF OCE 1232620. J.D.O. is supported by an Agouron Postdoctoral Fellowship. T.W.L. acknowledges support from the NSF-EAR and NASA-NAI. A.R. thanks the support of NERC via NE/J01043X/1.
    Description: 2015-11-13
    Keywords: I/Ca ; OAE 2 ; Oxygenation
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 4
    Publication Date: 2022-05-25
    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.
    Description: 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.
    Description: 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.
    Keywords: I/TOC ; Bottom water ; OAE 2 ; Black shale ; Baltic
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 5
    Publication Date: 2023-05-31
    Description: The decline in dissolved oxygen in global oceans (ocean deoxygenation) is a potential consequence of global warming which may have important impacts on ocean biogeochemistry and marine ecosystems. Current climate models do not agree on the trajectory of future deoxygenation on different timescales, in part due to uncertainties in the complex, linked effects of changes in ocean circulation, productivity and organic matter respiration. More (semi-)quantitative reconstructions of oceanic oxygen levels over the Pleistocene glacial cycles may provide a critical test of our mechanistic understanding of the response of oceanic oxygenation to climate change. Even the most promising proxies for bottom water oxygen (BWO) have limitations, which calls for new proxy development and a multi-proxy compilation to evaluate glacial ocean oxygenation. We use Holocene benthic foraminifera to explore I/Ca in Cibicidoides spp. as a BWO proxy. We propose that low I/Ca (e.g., 〈3 μmol/mol) in conjunction with benthic foraminiferal carbon isotope gradients and/or the surface pore area percentages in foraminiferal tests (e.g., 〉15%) may provide semi-quantitative estimates of low BWO in past oceans (e.g., 〈∼50 μmol/kg). We present I/Ca records in five cores and a global compilation of multiproxy data, indicating that bottom waters were generally less-oxygenated during glacial periods, with low O2 waters (〈∼50 μmol/kg) occupying some parts of the Atlantic and Pacific Oceans. Water mass ventilation and circulation may have been important in deoxygenation of the glacial deep Pacific and South Atlantic, whereas enhanced remineralization of organic matter may have had a greater impact on reducing the oxygen content of the interior Atlantic Ocean.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , peerRev
    Format: application/pdf
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  • 6
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    Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu
    Publication Date: 2022-10-31
    Description: Dataset: Atlantic croaker otolith geochemical concentrations
    Description: Geochemical concentrations (ppm) of six elements measured in otoliths of Atlantic croaker sampled on board of the R/V Oregon II during the NOAA Seamap Fall Groundfish Survey of 2014 (Oct 10 to Nov 4) and 2015 (Oct 8 to Nov 22). For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/784969
    Description: NSF Division of Ocean Sciences (NSF OCE) OCE-1633020
    Keywords: Hypoxia ; Gulf of Mexico ; Otolith ; Elements ; Atlantic Croaker
    Repository Name: Woods Hole Open Access Server
    Type: Dataset
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  • 7
    Publication Date: 2018-03-14
    Description: The sensitivity of sea level to melting from polar ice sheets and glaciers during recent natural and anthropogenic climate fluctuations is poorly constrained beyond the period of direct observation by satellite. We have investigated glacial meltwater events during the Anthropocene by adapting the pioneering approach of modeling trends in d18O in the pore waters of deep‐sea cores, previously used to constrain the size of ice sheets during the Last Glacial Maximum. We show that during recent warm periods, meltwater from glacier retreat drains into the coastal fjords, leaving a signature of depleted d18O values and low Cl concentrations in the pore water profiles of rapidly accumulating sediments. Here we model such pore water profiles in a piston core to constrain the timing and magnitude of an ice sheet retreat event at Caley Glacier on the west Antarctic Peninsula, and the result is compared with local ice front movement. This approach of pore water modeling was then applied in another kasten core and tested by a series of sensitivity analyses. The results suggest that our approach may be applied in fjords of different sedimentary settings to reconstruct the glacier history and allow insight into the sensitivity of polar glaciers to abrupt warming events.
    Type: Article , PeerReviewed
    Format: text
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  • 8
    Publication Date: 2019-09-23
    Description: We measured halogen concentrations and I-129/I ratios in five drilling sites of Integrated Ocean Drilling Program Expedition 311 (offshore Vancouver Island, Canada) in order to identify potential sources of fluids and methane in gas hydrate fields. Iodine is dominated by organic decomposition and transports with fluids in reducing environments and the presence of the cosmogenic radioisotope I-129 (T-1/2 = 15.7 Ma) allows the age determination of organic sources for iodine. Here we report halogen concentrations in 135 pore water samples, I concentrations in 48 sediment samples, and I-129/I ratios measured in a subset of 20 pore water samples. Most I-129/I ratios fall into a range around 500 x 10(-15), corresponding to a minimum age of 25 Ma and the lowest ratio of 188 x 10(-15) (T-min = 47 Ma) was observed at 208 m below sea floor (mbsf) in Site 1326. These ages are considerably older than that of the local sediments in the gas hydrate fields and that of the subducting sediments on the Juan de Fuca plate, indicating that old, accreted sediments in the accretionary wedge contribute a significant amount of iodide and, by association, of methane to the gas hydrate occurrences. A geochemical transport-reaction model was applied to simulate the advection of deeply sourced fluids and the release of iodide, bromide, and ammonia in the host sediments due to organic matter degradation. The model was first tested with data from two well studied areas, Ocean Drilling Program Site 1230 (Peru margin) and Site 1245 (Hydrate Ridge). The model results for the Expedition 311 sites indicate that the in situ release of young iodine is relatively minor in comparison to the contribution of migrating fluids, carrying large amounts of old iodine from deep sources. The comparison between the sites demonstrates that the total organic content has a strong effect on the rate of in situ iodine release and that lateral flows along fractures can have a significant influence on pore water chemistry, especially at the Cascadia margin. The iodine results indicate that mobilization and transport of methane from sources in the upper plate of active margins is an important process which can also play a substantial role in the formation of gas hydrate fields.
    Type: Article , PeerReviewed
    Format: text
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  • 9
    Publication Date: 2024-02-07
    Description: Planktic and benthic foraminiferal iodine (I) to calcium (Ca) molar ratios have been proposed as an exciting new proxy to assess subsurface and bottom water oxygenation in the past. Compared to trace metals, the analysis of iodine in foraminiferal calcite is more challenging, as iodine is volatile in acid solution. Here, we compare previous analyses that use tertiary amine with alternative analyses using tetramethylammonium hydroxide (TMAH) and ammonium hydroxide (NH4OH) to stabilize iodine in solution. In addition, we assess the effect of sample size and cleaning on planktic and benthic foraminiferal I/Ca. Our stabilization experiments with TMAH and NH4OH show similar trends as those using tertiary amine, giving relatively low I/Ca ratios for planktic and benthic foraminifera samples from poorly oxygenated waters, and high ratios for well-oxygenated waters. This suggests that both alternative methods are suitable to stabilize iodine initially dissolved in acid. Samples that contain 5–10 specimens show a wide spread in I/Ca. Samples containing 20 specimens or more show more centered I/Ca values, indicating that a larger sample size is more representative of the average planktic foraminifera community. The impact of cleaning on planktic and benthic foraminifera I/Ca ratios is very similar to Mg/Ca, with the largest effect occurring during the clay removal step. The largest iodine contaminations were recorded at locations characterized by moderate to high organic carbon contents. In those circumstances, we recommend doubling the oxidative cleaning steps (4 instead of 2 repetitions) to ensure that all organic material is removed.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
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  • 10
    Publication Date: 2011-09-01
    Description: We compare here results of iodine dating in fluids collected from mud volcanoes and gas hydrate occurrences associated with active margins. This is a compilation of previously reported data for 7 subduction zones around the Pacific Rim with slab ages ranging from 6 Ma to 130 Ma, where we determined iodine concentrations and 129I/I ratios in more than two hundred pore water samples. Iodine ages consistently are older than the host sediments and show an age distribution independent of the slab ages associated with the subduction zones. The results suggest that iodine in gas hydrates and mud volcanoes is predominantly derived from organic matter in the upper plates of subduction zones and that iodine derived from host sediments or subducting marine sediments has only a minor presence in these fluids. Because potential source sediments typically are found at lateral distances of 20 km or more, our results also suggest that fluid movement is possible over considerable distances in fractures present in the upper plate sediments. The association between iodine and methane suggests that our results can be extrapolated to the origin and transport of methane to mud volcanoes and gas hydrates. Throughout all studied sites around the Pacific margins, ages of source sediments for iodine were found to fall into the same range, which starts at the early Eocene ([~]50 Ma) and has a broad peak around 30 Ma. Our results indicate that the occurrence of iodine and methane in gas hydrates and mud volcanoes is the result of transport in aqueous fluids and long-term remobilization of carbon in the upper plates of subduction zones.
    Print ISSN: 0002-9599
    Electronic ISSN: 1945-452X
    Topics: Geosciences
    Published by HighWire Press on behalf of The American Journal of Science.
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