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  • Ocean Drilling Program; ODP  (2)
  • Magnesium
Collection
Keywords
Years
  • 1
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2006. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography 21 (2006): PA1007, doi:10.1029/2005PA001158.
    Description: Core top samples from Atlantic (Little Bahama Banks (LBB)) and Pacific (Hawaii and Indonesia) depth transects have been analyzed in order to assess the influence of bottom water temperature (BWT) and aragonite saturation levels on Mg/Ca and Sr/Ca ratios in the aragonitic benthic foraminifer Hoeglundina elegans. Both the Mg/Ca and Sr/Ca ratios in H. elegans tests show a general decrease with increasing water depth. Although at each site the decreasing trends are consistent with the in situ temperature profile, Mg/Ca and Sr/Ca ratios in LBB are substantially higher than in Indonesia and Hawaii at comparable water depths with a greater difference observed with increasing water depth. Because we find no significant difference between results obtained on “live” and “dead” specimens, we propose that these differences are due to primary effects on the metal uptake during test formation. Evaluation of the water column properties at each site suggests that in situ CO3 ion concentrations play an important role in determining the H. elegans Mg/Ca and Sr/Ca ratios. The CO3 ion effect is limited, however, only to aragonite saturation levels ([ΔCO3]aragonite) below 15 μmol kg−1. Above this level, temperature exerts a dominant effect. Accordingly, we propose that Mg/Ca and Sr/Ca in H. elegans tests can be used to reconstruct thermocline temperatures only in waters oversaturated with respect to the mineral aragonite using the following relationships: Mg/Ca = (0.034 ± 0.002)BWT + (0.96 ± 0.03) and Sr/Ca = (0.060 ± 0.002)BWT + (1.53 ± 0.03) (for [ΔCO3]aragonite 〉 15 μmol kg−1). The standard error associated with these equations is about ±1.1°C. Reconstruction of deeper water temperatures is complicated because in undersaturated waters, changes in Mg/Ca and Sr/Ca ratios reflect a combination of changes in [CO3] and BWT. Overall, we find that Sr/Ca, rather than Mg/Ca, in H. elegans may be a more accurate proxy for reconstructing paleotemperatures.
    Description: Yair Rosenthal acknowledges the support of Amtzia Genin and the Hebrew University, Forchheimer Fellowship, during his sabbatical in the Inter-University Institute in Eilat, Israel. This project has been funded by NSF Awards OCE 0220922 to Y.R. and OCE 0220776 to D.W.O. and B.K.L.
    Keywords: Benthic foraminifera ; Paleothermometry ; Magnesium
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 2
    Publication Date: 2024-01-09
    Description: Paired benthic foraminiferal trace metal and stable isotope records have been constructed from equatorial Pacific Ocean Drilling Program Site 1218. The records include the two largest abrupt (〈1 Myr) increases in the Cenozoic benthic oxygen isotope record: Oi‐1 in the earliest Oligocene (∼34 Ma) and Mi‐1 in the earliest Miocene (∼23 Ma). The paired Mg/Ca and oxygen isotope records are used to calculate seawater δ18O (δw). Calculated δw suggests that a large Antarctic ice sheet formed during Oi‐1 and subsequently fluctuated throughout the Oligocene on both short (〈0.5 Myr) and long (2–3 Myr) timescales, between about 50 and 100% of its maximum earliest Oligocene size. The magnitudes of these fluctuations are consistent with estimates of sea level derived from sequence stratigraphy. The transient expansion of the Antarctic ice sheet at Mi‐1 is marked in the benthic δ18O record by two positive excursions between 23.7 and 22.9 Ma, each with a duration of 200–300 kyr. Bottom water temperatures decreased by ∼2°C over the 150 kyr immediately prior to both rapid δ18O excursions. However, the onset of each of these phases of ice growth is synchronous, within the resolution of the records, with the onset of a 2°C warming over ∼150 kyr. We suggest that the warming during these glacial expansions reflect increased greenhouse forcing prompted by a sudden decrease in global chemical weathering rates as Antarctic basement silicate rocks became blanketed by an ice sheet. This represents a negative feedback process that might have operated during major abrupt growth phases of the Antarctic ice sheet.
    Keywords: Ocean Drilling Program; ODP
    Type: Dataset
    Format: application/zip, 3 datasets
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  • 3
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    PANGAEA
    In:  Supplement to: Greenop, Rosanna; Hain, Mathis P; Sosdian, Sindia M; Oliver, Kevin I C; Goodwin, Philip; Chalk, Thomas B; Lear, Caroline H; Wilson, Paul A; Foster, Gavin L (2017): A record of Neogene seawate d11B reconstructed from paired d11B analyses on benthic and planktic foraminifera. Climate of the Past, 13(2), 149-170, https://doi.org/10.5194/cp-13-149-2017
    Publication Date: 2024-01-09
    Description: The boron isotope composition (d11B) of planktic foraminiferal calcite, which reflects seawater pH, is a well-established proxy for reconstructing palaeo-atmospheric CO2 and seawater carbonate chemistry. However, to translate d11B measurements determined in calcareous fossils into pH we need to know the boron isotope composition of the parent seawater (d11Bsw). While a number of d11Bsw reconstructions exist, the discrepancies between them reveals uncertainties and deficiencies that need to be addressed. Here we present a new d11Bsw record based on the d11B difference between planktic and benthic foraminifera and an estimate of the pH gradient between surface and deep water. We then calculate d11Bsw two different ways. One variant of our method assumes that the pH gradient between surface and deep has remained the same as today over the past 23 Ma; the other uses the d13C gradient between surface and deep to represent change in the pH gradient through time. The results of these two methods of calculating d11Bsw are broadly consistency with each other, however, based on extensive carbon cycle modelling using CYCLOPS and GENIE we favour the d13C gradient method. In our favoured d11Bsw reconstruction, d11Bsw is around 2 per mil lower than today at ~37.5 per mil during the early and middle Miocene and increases to the modern value (39.61 per mil) by ~5 Ma. A similar pattern of change is evident in the seawater composition of three other stable isotope systems, Mg, Li and Ca. Concurrent shifts in the seawater isotopic composition of all four of these elements during the late Miocene, suggest a common forcing mechanism. We hypothesise the most likely cause of these shifts is a change in the isotopic composition of the riverine input, potentially driven by an increase in secondary mineral formation since ~15 Ma.
    Keywords: Ocean Drilling Program; ODP
    Type: Dataset
    Format: application/zip, 2 datasets
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