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Modeling the global ocean iron cycle (2010)

Parekh, Payal ; Follows, Michael J. ; Boyle, Edward A.

American Geophysical Union

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Publication Date: 2022-05-25

Description: Author Posting. © American Geophysical Union, 2004. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Global Biogeochemical Cycles 18 (2004): GB1002, doi:10.1029/2003GB002061.

Description: We describe a model of the ocean transport and biogeochemical cycling of iron and the subsequent control on export production and macronutrient distributions. Ocean transport of phosphorus and iron are represented by a highly idealized six-box ocean model. Export production is parameterized simply; it is limited by light, phosphate, and iron availability in the surface ocean. We prescribe the regional variations in aeolian deposition of iron and examine three parameterizations of iron cycling in the deep ocean: (1) net scavenging onto particles, the simplest model; (2) scavenging and desorption of iron to and from particles, analogous to thorium; and (3) complexation. Provided that some unknown parameter values can be set appropriately, all three biogeochemical models are capable of reproducing the broad features of the iron distribution observed in the modern ocean and explicitly lead to regions of elevated surface phosphate, particularly in the Southern Ocean. We compare the sensitivity of Southern Ocean surface macronutrient concentration to increased aeolian dust supply for each parameterization. Both scavenging-based representations respond to increasing dust supply with a drawdown of surface phosphate in an almost linear relationship. The complexation parameterization, however, asymptotes toward a limited drawdown of phosphate under the assumption that ligand production does not respond to increased dust flux. In the scavenging based models, deep water iron concentrations and, therefore, upwelled iron continually increase with greater dust supply. In contrast, the availability of complexing ligand provides an upper limit for the deep water iron concentration in the latter model.

Description: M. J. F. is grateful for funding from NOAA (NA16GP2988) and NSSF (OCE-336839). P. P. is grateful to the MIT Martin Fellowship and NASA Earth System Science Fellowship (NGT5- 30362) for funding.

Keywords: Modeling ; Ocean iron cycle

Repository Name: Woods Hole Open Access Server

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The 8200 year B.P. event in the slope water system, western subpolar North Atlantic (2010)

Keigwin, Lloyd D. ; Sachs, Julian P. ; Rosenthal, Yair ; [et al.]

American Geophysical Union

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Publication Date: 2022-05-25

Description: Author Posting. © American Geophysical Union, 2005. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography 20 (2005): PA2003, doi:10.1029/2004PA001074.

Description: Stable isotope, trace metal, alkenone paleothermometry, and radiocarbon methods have been applied to sediment cores in the western subpolar North Atlantic between Hudson Strait and Cape Hatteras to reveal the history of climate in that region over the past ∼11 kyr. We focus on cores from the Laurentian Fan, which is known to have rapid and continuous accumulation of hemipelagic sediment. Although results among our various proxy data are not always in agreement, the weight of the evidence (alkenone sea surface temperature (SST), δ18O and abundance of Globigerinoides ruber) indicates a continual cooling of surface waters over Laurentian Fan, from about 18°C in the early Holocene to about 8°C today. Alternatively, Mg/Ca data on planktonic foraminifera indicate no systematic change in Holocene SST. The inferred long-term decrease in SST was probably driven by decreasing seasonality of Northern Hemisphere insolation. Two series of proxy data show the gradual cooling was interrupted by a two-step cold pulse that began 8500 years ago, and lasted about 700 years. Although this event is associated with the final deglaciation of Hudson Bay, there is no δ18O minimum anywhere in the Labrador Sea, yet there is some evidence for it as far south as Cape Hatteras. Finally, although the 8200 year B.P. event has been implicated in decreasing North Atlantic ventilation, and hence widespread temperature depression on land and at sea, we find inconsistent evidence for a change at that time in deep ocean nutrient content at ∼4 km water depth.

Description: Funding for JPS was from the NOAA Climate and Global Change Program (NA 16GP2679), NSF-Earth System History (0116940), the Jeptha H. and Emily V. Wade Award for Research, and a Henry L. and Grace Doherty Professorship. LDK and YR were funded by NSF grant OCE-0117149.

Keywords: Lake Agassiz ; 8200 year event ; Meltwater pulse

Repository Name: Woods Hole Open Access Server

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Did North Atlantic overturning halt 17,000 years ago? (2010)

Keigwin, Lloyd D. ; Boyle, Edward A.

American Geophysical Union

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Publication Date: 2022-05-25

Description: Author Posting. © American Geophysical Union, 2008. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography 23 (2008): PA1101, doi:10.1029/2007PA001500.

Description: Models indicate that a complete shutdown of deep and intermediate water production is a possible consequence of extreme climate conditions in the northern North Atlantic, and the high ratio of 231Pa to 230Th on Bermuda Rise is evidence that this might have happened ∼17 ka during Heinrich event 1 (H1). However, new radiocarbon data from bivalves that lived at ∼4.6 km on the Bermuda Rise during H1 lead to a different conclusion. The bivalve data do indeed indicate ventilation of the deep western North Atlantic was suppressed during H1 but not as much as it was during the last glacial maximum. We propose that high diatom flux to the Bermuda Rise during H1 is at least in part responsible for increased 231Pa/230Th at that time. Although we cannot say for sure why opal production was so high in a gyre center location at that time, increased leakage of silica rich waters from the Southern Ocean to the North Atlantic is one possibility.

Description: This work was funded by a grant from the Comer Foundation to WHOI’s Ocean and Climate Change Institute.

Keywords: North Atlantic Ocean ; Meridional overturning ; Heinrich event

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The composition of dissolved iron in the dusty surface ocean : an exploration using size-fractionated iron-binding ligands (2014)

Fitzsimmons, Jessica N. ; Bundy, Randelle M. ; Al-Subiai, Sherain N. ; [et al.]

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Publication Date: 2022-05-25

Description: Author Posting. © The Author(s), 2014. This is the author's version of the work. It is posted here by permission of Elsevier for personal use, not for redistribution. The definitive version was published in Marine Chemistry 173 (2015): 125-135, doi:10.1016/j.marchem.2014.09.002.

Description: The size partitioning of dissolved iron and organic iron-binding ligands into soluble and colloidal phases was investigated in the upper 150 m of two stations along the GA03 U.S. GEOTRACES North Atlantic transect. The size fractionation was completed using cross-flow filtration methods, followed by analysis by isotope dilution inductively-coupled plasma mass spectrometry (ID-ICP-MS) for iron and competitive ligand exchange-adsorptive cathodic stripping voltammetry (CLE-ACSV) for iron-binding ligands. On average, 80% of the 0.1-0.65 nM dissolved iron (〈0.2 μm) was partitioned into the colloidal iron (cFe) size fraction (10 kDa 〈 cFe 〈 0.2 μm), as expected for areas of the ocean underlying a dust plume. The 1.3-2.0 nM strong organic iron-binding ligands, however, overwhelmingly (75-77%) fell into the soluble size fraction (〈10 kDa). As a result, modeling the dissolved iron size fractionation at equilibrium using the observed ligand partitioning did not accurately predict the iron partitioning into colloidal and soluble pools. This suggests that either a portion of colloidal ligands are missed by current electrochemical methods because they react with iron more slowly than the equilibration time of our CLE-ACSV method, or part of the observed colloidal iron is actually inorganic in composition and thus cannot be predicted by our model of unbound iron-binding ligands. This potentially contradicts the prevailing view that greater than 99% of dissolved iron in the ocean is organically complexed. Untangling the chemical form of iron in the upper ocean has important implications for surface ocean biogeochemistry and may affect iron uptake by phytoplankton.

Description: J.N. Fitzsimmons was funded by a National Science Foundation Graduate Research Fellowship (NSF Award #0645960). Research funding was provided by the National Science Foundation (OCE #0926204 and OCE #0926197) and the Center for Microbial Oceanography: Research and Education (NSF-OIA Award #EF-0424599) to E.A. Boyle. R.M. Bundy was partially funded by NSF OCE-0550302 and NSF OCE-1233733 to K.A. Barbeau and an NSF-GK12 graduate fellowship.

Keywords: Iron ; Iron ligands ; CLE-ACSV ; Colloids ; Ultrafiltration ; Trace metals ; GEOTRACES ; North Atlantic Ocean ; Chemical oceanography

Repository Name: Woods Hole Open Access Server

Type: Preprint

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GEOTRACES IC1 (BATS) contamination-prone trace element isotopes Cd, Fe, Pb, Zn, Cu, and Mo intercalibration (2014)

Boyle, Edward A. ; John, Seth G. ; Abouchami, Wafa ; [et al.]

Association for the Sciences of Limnology and Oceanography

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Publication Date: 2022-05-26

Description: Author Posting. © Association for the Sciences of Limnology and Oceanography, 2012. This article is posted here by permission of Association for the Sciences of Limnology and Oceanography for personal use, not for redistribution. The definitive version was published in Limnology and Oceanography: Methods 10 (2012): 653-665, doi:10.4319/lom.2012.10.653.

Description: We report data on the isotopic composition of cadmium, copper, iron, lead, zinc, and molybdenum at the GEOTRACES IC1 BATS Atlantic intercalibration station. In general, the between lab and within-lab precisions are adequate to resolve global gradients and vertical gradients at this station for Cd, Fe, Pb, and Zn. Cd and Zn isotopes show clear variations in the upper water column and more subtle variations in the deep water; these variations are attributable, in part, to progressive mass fractionation of isotopes by Rayleigh distillation from biogenic uptake and/or adsorption. Fe isotope variability is attributed to heavier crustal dust and hydrothermal sources and light Fe from reducing sediments. Pb isotope variability results from temporal changes in anthropogenic source isotopic compositions and the relative contributions of U.S. and European Pb sources. Cu and Mo isotope variability is more subtle and close to analytical precision. Although the present situation is adequate for proceeding with GEOTRACES, it should be possible to improve the within-lab and between-lab precisions for some of these properties.

Description: The National Science Foundation sponsored the cruise and many of the shipboard participants; in particular E.B. was funded to participate on the cruise by NSF Grant OCE-0751409 and his preparation of this paper was partially supported by grants from the Kuwait Foundation for the Advancement of Science (KFAS) and the Singapore-MIT Alliance for Research and Technology (SMART).

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