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  • 1
    Publication Date: 2022-05-25
    Description: © The Author(s), 2017. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Nature Communications 8 (2017): 844, doi:10.1038/s41467-017-00853-5.
    Description: Authigenic clay minerals formed on or in the seafloor occur in every type of marine sediment. They are recognized to be a major sink of many elements in the ocean but are difficult to study directly due to dilution by detrital clay minerals. The extremely low dust fluxes and marine sedimentation rates in the South Pacific Gyre (SPG) provide a unique opportunity to examine relatively undiluted authigenic clay. Here, using Mg isotopes and element concentrations combined with multivariate statistical modeling, we fingerprint and quantify the abundance of authigenic clay within SPG sediment. Key reactants include volcanic ash (source of reactive aluminium) and reactive biogenic silica on or shallowly buried within the seafloor. Our results, together with previous studies, suggest that global reorganizations of biogenic silica burial over the Cenozoic reduced marine authigenic clay formation, contributing to the rise in seawater Mg/Ca and decline in atmospheric CO2 over the past 50 million years.
    Description: Funding for this research was provided by the U.S. National Science Foundation to R.W.M. (OCE1130531) and to J.A.H. (OCE1654571).
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 2
    Publication Date: 2022-05-26
    Description: © The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Mayfield, K. K., Eisenhauer, A., Santiago Ramos, D. P., Higgins, J. A., Horner, T. J., Auro, M., Magna, T., Moosdorf, N., Charette, M. A., Gonneea, M. E., Brady, C. E., Komar, N., Peucker-Ehrenbrink, B., & Paytan, A. Groundwater discharge impacts marine isotope budgets of Li, Mg, Ca, Sr, and Ba. Nature Communications, 12(1), (2021): 148-020-20248-3, doi:10.1038/s41467-020-20248-3.
    Description: Groundwater-derived solute fluxes to the ocean have long been assumed static and subordinate to riverine fluxes, if not neglected entirely, in marine isotope budgets. Here we present concentration and isotope data for Li, Mg, Ca, Sr, and Ba in coastal groundwaters to constrain the importance of groundwater discharge in mediating the magnitude and isotopic composition of terrestrially derived solute fluxes to the ocean. Data were extrapolated globally using three independent volumetric estimates of groundwater discharge to coastal waters, from which we estimate that groundwater-derived solute fluxes represent, at a minimum, 5% of riverine fluxes for Li, Mg, Ca, Sr, and Ba. The isotopic compositions of the groundwater-derived Mg, Ca, and Sr fluxes are distinct from global riverine averages, while Li and Ba fluxes are isotopically indistinguishable from rivers. These differences reflect a strong dependence on coastal lithology that should be considered a priority for parameterization in Earth-system models.
    Description: We thank A. Beck, H. Dulai, I. Santos, C. Benitez-Nelson, W. Moore, A. Martin, and H. Windom for sample access. We also thank A. Kolevica, A. Heuser, H. Pryer, J. Middleton, R. Franks, F. Lon, N. Slater, and O. Šebek for their laboratory and analytical assistance. This material is based upon research supported by the National Science Foundation Graduate Research Fellowship Program and an internship provided through the U.S. Geological Survey Graduate Research Internship Program (GRIP). This research was also supported by grants from: the German Academic Exchange Service (DAAD), Northern California chapter of the Achievement Rewards for College Scientists Foundation, International Association of GeoChemistry, Geological Society of America, Northern California Geological Society, Myers Trust, Friends of Long Marine Lab, and UC MEXUS (to K.K.M.). We acknowledge funding from EU-ITN Horizon project 643084 (to A.E. and T.M.) and NSF grant Award Number 1259440 (to A.P.). We also acknowledge funding from NSF grant award number OCE-1736949 (to T.J.H.). Any use of trade, firm or product names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 3
    Publication Date: 2022-10-26
    Description: Author Posting. © American Geophysical Union, 2021. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Solid Earth 126(2), (2021): e2020JB020237, https://doi.org/10.1029/2020JB020237.
    Description: Alteration of mantle peridotite in the Samail ophiolite forms secondary minerals, mainly serpentine and Mg‐rich carbonates. Magnesium accounts for ∼25 – 30% of peridotite mass and its mobility can be used to trace this alteration. We report the first set of Mg isotope measurements from peridotites and their alteration products in Oman. Partially serpentinized peridotites have Mg isotope ratios that are indistinguishable from estimates for the average mantle and bulk silicate earth (δ26Mg = −0.25 ± 0.04‰). However, more extensively altered peridotite samples show large shifts in Mg isotopic composition. The range of δ26Mg values for our suite of alteration products from the mantle section is ∼4.5‰ (from −3.39‰ to 1.19‰), or 〉60% of the total range of terrestrial variability in δ26Mg values. Serpentine veins are typically enriched in 26Mg (max δ26Mg value = 0.96‰) whereas Mg‐carbonate veins are associated with low 26Mg/24Mg ratios (magnesite δ26Mg = −3.3‰, dolomite δ26Mg = −1.91‰). Our preferred explanation for the range in δ26Mg values involves coprecipitation of serpentine and carbonates at water‐to‐rock ratios 〉103. The coincidence of alteration products characterized by δ26Mg values that are both lower and higher than bulk silicate Earth and the finite 14C ages of the carbonates suggest that both serpentinization and carbonation are ongoing in Oman. Rates of calcite precipitation in travertines inferred from Δ26Mgcal‐fl suggest that travertine formation in Oman sequesters a total of 106–107 kg CO2/yr, consistent with previous estimates.
    Description: This work was supported through the Sloan Foundation–Deep Carbon Observatory (Grant 2014‐3‐01, Kelemen PI), the U.S.‐National Science Foundation (NSF‐EAR‐1516300, Kelemen lead PI).
    Description: 2021-06-04
    Keywords: Carbonation ; Mg isotopes ; Oman ; Ophiolite ; Peridotite ; Serpentinization
    Repository Name: Woods Hole Open Access Server
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  • 4
    Publication Date: 2024-02-05
    Description: This table includes temperatures calculated from organic biomarker (TEX86) measurements performed on Paleocene, Eocene and Oligocene sediment material from Ocean Drilling Program (ODP) Hole 198-1209A, Shatsky Rise.
    Keywords: 198-1209A; Acyclic glycerol dialkyl glycerol tetraether, fractional abundance; AGE; Biomarker; Branched and isoprenoid tetraether index; Calculated; Calculated according to Schouten et al. (2002); Calculated after Hopmans et al. (2004); Calculated after Zhang et al. (2011); Calculated after Zhang et al. (2016); Calculated from TEX86 (Tierney and Tingley, 2014, 2015); Calculated from TEX86H (Kim et al., 2010); Cenozoic; Crenarchaeol, fractional abundance; Crenarchaeol isomer, fractional abundance; Depth, composite; DEPTH, sediment/rock; Dicyclic glycerol dialkyl glycerol tetraether, fractional abundance; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Eocene; IODP Depth Scale Terminology; Joides Resolution; Leg198; Methane index; Monocyclic glycerol dialkyl glycerol tetraether, fractional abundance; North Pacific Ocean; ODP 1209; Oligocene; Pacific; Paleocene; Ratio; Ring index; Ring index of tetraether index of 86 carbon atoms; Sample code/label; Sea surface temperature; Tetraether index of 86 carbon atoms; TEX86; Tricyclic glycerol dialkyl glycerol tetraether, fractional abundance; upper ocean temperatures; ΔRing index
    Type: Dataset
    Format: text/tab-separated-values, 874 data points
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Mathematische Zeitschrift 115 (1970), S. 366-370 
    ISSN: 1432-1823
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 27 (1982), S. 476-478 
    ISSN: 1573-2568
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
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    Elsevier
    In:  Earth and Planetary Science Letters, 245 (3-4). pp. 523-537.
    Publication Date: 2020-06-02
    Description: Extreme global warmth and an abrupt negative carbon isotope excursion during the Paleocene–Eocene Thermal Maximum (PETM) have been attributed to a massive release of methane hydrate from sediments on the continental slope [1]. However, the magnitude of the warming (5 to 6 °C [2],[3]) and rise in the depth of the CCD (〉 2 km; [4]) indicate that the size of the carbon addition was larger than can be accounted for by the methane hydrate hypothesis. Additional carbon sources associated with methane hydrate release (e.g. pore-water venting and turbidite oxidation) are also insufficient. We find that the oxidation of at least 5000 Gt C of organic carbon is the most likely explanation for the observed geochemical and climatic changes during the PETM, for which there are several potential mechanisms. Production of thermogenic CH4 and CO2 during contact metamorphism associated with the intrusion of a large igneous province into organic rich sediments [5] is capable of supplying large amounts of carbon, but is inconsistent with the lack of extensive carbon loss in metamorphosed sediments, as well as the abrupt onset and termination of carbon release during the PETM. A global conflagration of Paleocene peatlands [6] highlights a large terrestrial carbon source, but massive carbon release by fire seems unlikely as it would require that all peatlands burn at once and then for only 10 to 30 ky. In addition, this hypothesis requires an order of magnitude increase in the amount of carbon stored in peat. The isolation of a large epicontinental seaway by tectonic uplift associated with volcanism or continental collision, followed by desiccation and bacterial respiration of the aerated organic matter is another potential mechanism for the rapid release of large amounts of CO2. In addition to the oxidation of the underlying marine sediments, the desiccation of a major epicontinental seaway would remove a large source of moisture for the continental interior, resulting in the desiccation and bacterial oxidation of adjacent terrestrial wetlands.
    Type: Article , PeerReviewed
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  • 8
    Publication Date: 2023-02-08
    Description: Low-temperature (〈100 °C) alteration of oceanic crust plays an important role in determining the chemical composition of the oceans. Although a major sink of seawater potassium, little is known about the effects of low-temperature basalt alteration on the potassium isotopic composition of seawater (K∼0‰), which is ∼0.50‰ enriched relative to bulk silicate Earth (BSE, K= -0.54‰). Here, we present a suite of isotopic systems (K, Mg, Li, 87Sr/86Sr) and major/minor elements in bulk rock, veins and mineral separates from the upper volcanic section of Cretaceous (Troodos ophiolite) and Jurassic (Ocean Drilling Program Hole 801C) oceanic crust. We use these data to estimate the K isotopic fractionation associated with low-temperature oceanic crust alteration and provide new constraints on the role of this process in the global geochemical cycles of Mg and K in seawater. We find that hydrothermally altered basalts from the Troodos ophiolite and ODP Hole 801C, most of which are enriched in K relative to the unaltered glass compositions, have K values both higher and lower than BSE, ranging from +0.01‰ to -1.07‰ (n=83) and +0.04‰ to -0.88‰ (n=17), respectively. Average K values of bulk-rock samples from Troodos and Hole 801C are indistinguishable from each other at ∼-0.50‰, indicating that low-temperature basalt alteration is a sink of 39K from seawater, and explaining, in part, why seawater has a higher 41K/39K than BSE. In contrast to K, average Mg values for both Troodos (∼0.00‰) and Hole 801C (∼0.20‰) indicate that altered oceanic crust (AOC) is a sink of 26Mg from seawater, likely contributing to the light Mg composition of seawater (∼-0.8‰) relative to BSE (∼-0.2‰). We observe isotopically heavy Mg values in basalt samples characterized by small to no changes in bulk Mg content, consistent with extensive isotopic exchange of Mg between seawater and oceanic crust during low-temperature oceanic crust alteration. Finally, we find that variability in Li and K across three sites in the Troodos ophiolite can be explained by different styles of alteration that appear to be related to the timing of sedimentation and its effects on chemical and isotopic exchange between seawater and oceanic crust.
    Type: Article , PeerReviewed
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  • 9
    Publication Date: 2024-02-07
    Description: Groundwater-derived solute fluxes to the ocean have long been assumed static and subordinate to riverine fluxes, if not neglected entirely, in marine isotope budgets. Here we present concentration and isotope data for Li, Mg, Ca, Sr, and Ba in coastal groundwaters to constrain the importance of groundwater discharge in mediating the magnitude and isotopic composition of terrestrially derived solute fluxes to the ocean. Data were extrapolated globally using three independent volumetric estimates of groundwater discharge to coastal waters, from which we estimate that groundwater-derived solute fluxes represent, at a minimum, 5% of riverine fluxes for Li, Mg, Ca, Sr, and Ba. The isotopic compositions of the groundwater-derived Mg, Ca, and Sr fluxes are distinct from global riverine averages, while Li and Ba fluxes are isotopically indistinguishable from rivers. These differences reflect a strong dependence on coastal lithology that should be considered a priority for parameterization in Earth-system models.
    Type: Article , PeerReviewed
    Format: text
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