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  • Iron isotopes  (2)
  • 11-105; 129-801C; 185-1149A; 185-1149C; 22-216; 40-364; 92-597C; Comment; Copper; Deep Sea Drilling Project; DRILL; Drilling/drill rig; DSDP; DSDP/ODP/IODP sample designation; Event label; Glomar Challenger; Indian Ocean//RIDGE; Joides Resolution; Leg11; Leg129; Leg185; Leg22; Leg40; Leg92; North Atlantic/HILL; North Pacific Ocean; Number; Sample code/label; Sample material; South Atlantic/SYNCLINE; South Pacific; δ65Cu; δ65Cu, standard deviation  (1)
  • 123-765D; Aluminium oxide; Calcium oxide; Calculated; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Inductively coupled plasma atomic emission spectroscope (ICP-AES); Inductively coupled plasma - mass spectrometry (ICP-MS); Iron oxide, Fe2O3; Iron oxide, FeO; Joides Resolution; Leg123; Loss on ignition; Magnesium oxide; Manganese oxide; Ocean Drilling Program; ODP; Phosphorus pentoxide; Potassium oxide; Rock type; Sample code/label; Sample type; Silicon dioxide; Sodium oxide; South Indian Ridge, South Indian Ocean; Sum; Titanium dioxide; δ57Fe  (1)
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  • 1
    Publication Date: 2023-06-27
    Keywords: 11-105; 129-801C; 185-1149A; 185-1149C; 22-216; 40-364; 92-597C; Comment; Copper; Deep Sea Drilling Project; DRILL; Drilling/drill rig; DSDP; DSDP/ODP/IODP sample designation; Event label; Glomar Challenger; Indian Ocean//RIDGE; Joides Resolution; Leg11; Leg129; Leg185; Leg22; Leg40; Leg92; North Atlantic/HILL; North Pacific Ocean; Number; Sample code/label; Sample material; South Atlantic/SYNCLINE; South Pacific; δ65Cu; δ65Cu, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 102 data points
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  • 2
    Publication Date: 2024-04-16
    Keywords: 123-765D; Aluminium oxide; Calcium oxide; Calculated; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Inductively coupled plasma atomic emission spectroscope (ICP-AES); Inductively coupled plasma - mass spectrometry (ICP-MS); Iron oxide, Fe2O3; Iron oxide, FeO; Joides Resolution; Leg123; Loss on ignition; Magnesium oxide; Manganese oxide; Ocean Drilling Program; ODP; Phosphorus pentoxide; Potassium oxide; Rock type; Sample code/label; Sample type; Silicon dioxide; Sodium oxide; South Indian Ridge, South Indian Ocean; Sum; Titanium dioxide; δ57Fe
    Type: Dataset
    Format: text/tab-separated-values, 102 data points
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  • 3
    Publication Date: 2022-05-25
    Description: Author Posting. © The Author(s), 2009. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Geochimica et Cosmochimica Acta 73 (2009): 4045-4059, doi:10.1016/j.gca.2009.04.026.
    Description: Recent studies have suggested that rivers may present an isotopically light Fe source to the oceans. Since the input of dissolved iron from river water is generally controlled by flocculation processes that occur during estuarine mixing, it is important to investigate potential fractionation of Fe-isotopes during this process. In this study, we investigate the influence of the flocculation of Fe-rich colloids on the iron isotope composition of pristine estuarine waters and suspended particles. The samples were collected along a salinity gradient from the fresh water to the ocean in the North River estuary (MA, USA). Estuarine samples were filtered at 0.22 μm and the iron isotope composition of the two fractions (dissolved and particles) were analyzed using high resolution MC-ICP-MS after chemical purification. Dissolved iron results show positive δ56Fe values (with an average of 0.43 ± 0.04 ‰) relative to the IRMM-14 standard and do not display any relationships with salinity or with percentage of colloid flocculation. The iron isotopic composition of the particles suspended in fresh water is characterized by more negative δ56Fe values than for dissolved Fe and correlate with the percentage of Fe flocculation. Particulate δ56Fe values vary from -0.09‰ at no flocculation to ~ 0.1‰ at the flocculation maximum, which reflect mixing effects between river-borne particles, lithogenic particles derived from coastal seawaters and newly precipitated colloids. Since the process of flocculation produces minimal Fe-isotope fractionation in the dissolved Fe pool, we suggest that the pristine iron isotope composition of fresh water is preserved during estuarine mixing and that the value of the global riverine source into the ocean can be identified from the fresh water values. However, this study also suggests that δ56Fe composition of rivers can also be characterized by more positive δ56Fe values (up to 0.3 per mil) relative to the crust than previously reported. In order to improve our current understanding of the oceanic iron isotope cycling, further work is now required to determine the processes controlling the fractionation of Fe isotopes during continental run-off.
    Description: This study was supported by the National Science Foundation (OCE 0550066) to O. Rouxel and Edward Sholkovitz.
    Keywords: Iron isotopes ; Rivers ; Estuary ; Flocculation ; Iron cycle ; Colloids
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 4
    Publication Date: 2022-05-26
    Description: Author Posting. © Elsevier B.V., 2008. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Chemical Geology 252 (2008): 214-227, doi:10.1016/j.chemgeo.2008.03.009.
    Description: In this study, we report on coupled Fe- and S-isotope systematics of hydrothermal fluids and sulfide deposits from the East Pacific Rise at 9-10°N to better constrain processes affecting Fe- isotope fractionation in hydrothermal environments. We aim to address three fundamental questions: (1) is there significant Fe isotope fractionation during sulfide precipitation? (2) Is there significant variability of Fe-isotope composition of the hydrothermal fluids reflecting sulfide precipitation in subsurface environments? (3) Are there any systematics between Fe- and S- isotopes in sulfide minerals? The results show that chalcopyrite, precipitating in the interior wall of a hydrothermal chimney displays a limited range of δ56Fe values and δ34S values, between –0.11 to –0.33‰ and 2.2 to 2.6‰ respectively. The δ56Fe values are, on average, slightly higher by 0.14‰ relative to coeval vent fluid composition while δ34S values suggest significant S-isotope fractionation (-0.6±0.2‰) during chalcopyrite precipitation. In contrast, systematically lower δ56Fe and δ34S values relative to hydrothermal fluids, by up to 0.91‰ and 2.0‰ respectively, are observed in pyrite and marcasite precipitating in the interior of active chimneys. These results suggest isotope disequilibrium in both Fe- and S-isotopes due to S-isotopic exchange between hydrothermal H2S and seawater SO42- followed by rapid formation of pyrite from FeS precursors, thus preserving the effects of a strong kinetic Fe-isotope fractionation during FeS precipitation. In contrast, δ56Fe and δ34S values of pyrite from inactive massive sulfides, which show evidence of extensive late-stage reworking, are essentially similar to the hydrothermal fluids. Multiple stages of remineralization of ancient chimney deposits at the seafloor appear to produce minimal Fe-isotope fractionation. Similar affects are indicated during subsurface sulfide precipitation as demonstrated by the lack of systematic differences between δ56Fe values in both high-temperature, Fe-rich black smokers and lower temperature, Fe-depleted vents.
    Description: Support for W. Bach and K. Edwards was provided by NSF grant OCE-0241791 and support for O. Rouxel was provided by funding from the WHOI Deep Ocean Exploration Institute and NSF grant OCE-0622982 and OCE-0647948.
    Keywords: Iron isotopes ; Sulfur isotopes ; Hydrothermal systems ; Sulfide deposits
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
    Format: application/pdf
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