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  • 1
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    Th-234 sorption and export models in the water column : a review (2006)
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    Publication Date: 2022-05-25
    Description: Author Posting. © The Authors, 2005. 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 Marine Chemistry 100 (2006): 234-249, doi:10.1016/j.marchem.2005.10.014.
    Description: Over the past few decades, the radioisotope pair of 238U/234Th has been widely and increasingly used to describe particle dynamics and particle export fluxes in a variety of aquatic systems. The present paper is one of five review articles dedicated to 234Th. It is focused on the models associated with 234Th whereas the companion papers (same issue) are focused on present and future methodologies and techniques (Rutgers van der Loeff et al.), C/234Th ratios (Buesseler et al.), 234Th speciation (Santschi et al.) and present and future applications of 234Th (Waples et al.). In this paper, we review current 234Th scavenging models and discuss the relative importance of the non steady state and physical terms associated with the most commonly used model to estimate 234Th flux. Based on this discussion we recommend that for future work the use of models should be accompanied by a discussion of the effect that model and data uncertainty have on the model results. We also suggest that future field work incorporate repeat occupations of sample sites on time scales of 1-4 weeks in order to evaluate steady state versus non steady state estimates of 234Th export, especially during high flux events (〉 ca. 800 dpm m-2 d-1). Finally, knowledge of the physical oceanography of the study area is essential, particularly in ocean margins and in areas of established upwelling (e.g. Equatorial Pacific). These suggestions will greatly enhance the application of 234Th as a tracer of particle dynamics and flux in more complicated regimes.
    Description: This paper grew out of discussion held at the “Future Applications of 234Th in Aquatic Systems” workshop held at Woods Hole Oceanographic Institution in August, 2004 (see: http://www.geol.sc.edu/cbnelson/Thmeeting/). We are grateful to the US National Science Foundation Chemical Oceanography Program (OCE 0354757) for its support of the workshop. We thank the US National Science Foundation, the National Oceanic and Atmospheric Administration and the Belgian Science Policy for their support of many of the field and modeling efforts described in this paper.
    Keywords: Th-234 ; Model ; Scavenging ; Export ; Particle dynamics
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 2
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    A review of present techniques and methodological advances in analyzing Th-234 in aquatic systems (2006)
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    Publication Date: 2022-05-26
    Description: Author Posting. © The Authors, 2005. 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 Marine Chemistry 100 (2006): 190-212, doi:10.1016/j.marchem.2005.10.012.
    Description: The short-lived thorium isotope 234Th (half-life 24.1 days) has been used as a tracer for a variety of transport processes in aquatic systems. Its use as a tracer of oceanic export via sinking particles has stimulated a rapidly increasing number of studies that require analyses of 234Th in both marine and freshwater systems. The original 234Th method is labour intensive. Thus, there has been a quest for simpler techniques that require smaller sample volumes. Here, we review current methodologies in the collection and analysis of 234Th from the water column, discuss their individual strengths and weaknesses, and provide an outlook on possible further improvements and future challenges. Also included in this review are recommendations on calibration procedures and the production of standard reference materials as well as a flow chart designed to help researchers find the most appropriate 234Th analytical technique for a specific aquatic regime and known sampling constraints.
    Description: Individuals and science efforts discussed herein were supported by many national science programs, including the U.S. National Science Foundation and U.S. Department of Energy and the Ministerio de Educación y Ciencia of Spain. The Agency is grateful for the support provided to its Marine Environment Laboratory by the Government of the Principality of Monaco".
    Keywords: Th-234 ; Methodology ; Sampling ; Analytical techniques, ; Export
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
    Format: 327450 bytes
    Format: 289061 bytes
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  • 3
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    Flux of particulate elements in the North Atlantic Ocean constrained by multiple radionuclides (2019)
    American Geophysical Union
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    Publication Date: 2022-10-26
    Description: Author Posting. © American Geophysical Union, 2019. 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 32(12), (2019): 1738-1758, doi:10.1029/2018GB005994.
    Description: Sinking particles strongly regulate the distribution of reactive chemical substances in the ocean, including particulate organic carbon and other elements (e.g., P, Cd, Mn, Cu, Co, Fe, Al, and 232Th). Yet, the sinking fluxes of trace elements have not been well described in the global ocean. The U.S. GEOTRACES campaign in the North Atlantic (GA03) offers the first data set in which the sinking flux of carbon and trace elements can be derived using four different radionuclide pairs (238U:234Th ;210Pb:210Po; 228Ra:228Th; and 234U:230Th) at stations co‐located with sediment trap fluxes for comparison. Particulate organic carbon, particulate P, and particulate Cd fluxes all decrease sharply with depth below the euphotic zone. Particulate Mn, Cu, and Co flux profiles display mixed behavior, some cases reflecting biotic remineralization, and other cases showing increased flux with depth. The latter may be related to either lateral input of lithogenic material or increased scavenging onto particles. Lastly, particulate Fe fluxes resemble fluxes of Al and 232Th, which all have increasing flux with depth, indicating a dominance of lithogenic flux at depth by resuspended sediment transported laterally to the study site. In comparing flux estimates derived using different isotope pairs, differences result from different timescales of integration and particle size fractionation effects. The range in flux estimates produced by different methods provides a robust constraint on the true removal fluxes, taking into consideration the independent uncertainties associated with each method. These estimates will be valuable targets for biogeochemical modeling and may also offer insight into particle sinking processes.
    Description: This study grew out of a synthesis workshop at the Lamont‐Doherty Earth Observatory of Columbia University in August 2016. This workshop was sponsored by the U.S. GEOTRACES Project Office (NSF 1536294) and the Ocean Carbon and Biogeochemistry (OCP) Project Office (NSF 1558412 and NASA NNX17AB17G). The U.S. National Science Foundation supported all of the analytical work on GA03. Kuanbo Zhou measured 228Th in the large size class particles (NSF 0925158 to WHOI). NSF 1061128 to Stony Brook University supported the BaRFlux project, for which Chistina Heilbrun is acknowledged for laboratory and field work. The lead author acknowledges support from a start‐up grant from the University of Southern Mississippi. Two anonymous reviewers are thanked for their constructive comments. All GEOTRACES GA03 data used in this study are accessible through the Biological and Chemical Oceanography Data Management Office (http://data.bco‐dmo.org/jg/dir/BCO/GEOTRACES/NorthAtlanticTransect/), and derived parameters are reported in the supporting information.
    Description: 2019-05-22
    Keywords: Biological carbon pump ; Trace metals ; North Atlantic ; Export ; GEOTRACES
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 4
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    Ironing out Fe residence time in the dynamic upper ocean (2020)
    American Geophysical Union
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    Publication Date: 2022-10-26
    Description: © The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Black, E. E., Kienast, S. S., Lemaitre, N., Lam, P. J., Anderson, R. F., Planquette, H., Planchon, F., & Buesseler, K. O. Ironing out Fe residence time in the dynamic upper ocean. Global Biogeochemical Cycles, 34(9), (2020): e2020GB006592, doi:10.1029/2020GB006592.
    Description: Although iron availability has been shown to limit ocean productivity and influence marine carbon cycling, the rates of processes driving iron's removal and retention in the upper ocean are poorly constrained. Using 234Th‐ and sediment‐trap data, most of which were collected through international GEOTRACES efforts, we perform an unprecedented observation‐based assessment of iron export from and residence time in the upper ocean. The majority of these new residence time estimates for total iron in the surface ocean (0–250 m) fall between 10 and 100 days. The upper ocean residence time of dissolved iron, on the other hand, varies and cycles on sub‐annual to annual timescales. Collectively, these residence times are shorter than previously thought, and the rates and timescales presented here will contribute to ongoing efforts to integrate iron into global biogeochemical models predicting climate and carbon dioxide sequestration in the ocean in the 21st century and beyond.
    Description: We would like to thank S. Albani for providing the dust model results (Community Atmosphere Model, C4fn) and the three anonymous reviewers for their constructive comments. The U.S. GEOTRACES work was supported by the National Science Foundation (OCE‐1232669 and OCE‐1518110) and E. Black was also funded by a NASA Earth and Space Science Graduate Fellowship (NNX13AP31H) and the Ocean Frontier Institute. The GEOVIDE work was funded by the Flanders Research Foundation (G071512N), the Vrije Universiteit Brussel (SRP‐2), the French ANR Blanc GEOVIDE (ANR‐13‐BS06‐0014), ANR RPDOC BITMAP (ANR‐12‐PDOC‐0025‐01), IFREMER, CNRS‐INSU (programme LEFE), INSU OPTIMISP, and Labex‐Mer (ANR‐10‐LABX‐19).
    Keywords: Thorium‐234 ; Iron ; Export ; GEOTRACES ; Residence time
    Repository Name: Woods Hole Open Access Server
    Type: Article
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