132 research outputs found
Recommended from our members
Biogeochemical Studies of the South Pacific Ocean Using Thorium and Protactinium Isotopes
The ocean is both a repository and reactor for chemicals at the Earth’s surface. As chemicals enter the ocean they are taken up by organisms, transported by currents, reacted with particle surfaces, and eventually buried at the seafloor. This dynamic set of chemical processes and exchanges are encapsulated by the term biogeochemistry.
Marine biogeochemistry can be broadly deconstructed into two parts: ocean interfaces and internal cycling. Ocean interfaces are where chemical constituents enter and leave the ocean, including the air-sea boundary, mid-ocean ridges, continental margins, and rivers. Internal cycling is how chemical constituents are reacted, transported, taken up by organisms, and redistributed within the ocean. For a complete understanding of marine biogeochemical cycles, the input, output, and internal cycling rates of major and trace elements must be quantified. However, this rate information is difficult to infer from the observational snapshots of chemical concentrations typically collected on oceanographic expeditions.
The long-lived radioisotopes of thorium (Th) and protactinium (Pa) provide an opportunity to quantify these elusive biogeochemical rates. The radiogenic isotopes 230Th and 231Pa are produced at a uniform rate throughout the water column by uranium decay. A third isotope, 232Th, is primordial and brought to the ocean by the dissolution of lithogenic matter. While uranium is highly soluble, Th and Pa are highly insoluble, and are rapidly removed from solution by adsorption onto settling particle matter. Due to their insolubility and known input rates, 230Th and 231Pa have well-constrained 1-d mass budgets between radiogenic production and scavenging removal.
This thesis explores new ways Th and Pa isotopes can be used to understand and quantify rates of biogeochemical processes in the South Pacific Ocean, and to assess how measurements of sedimentary Th and Pa isotopes can be used to study these processes in the geologic past. In chapter 1, I characterize the effects of submarine hydrothermal activity on the distributions of 230Th and 231Pa, finding strong removal due to adsorption by Fe and Mn oxide particles. In chapter two, I utilize the radioactive disequilibria of two additional radiogenic thorium isotopes with much shorter half-lives, 234Th and 228Th, to constrain the kinetics of Th scavenging by hydrothermal particles.
Chapter three switches gears towards quantifying the internal cycling of particulate organic carbon in the subtropical South Pacific. Using a new method based on measurements of particulate 230Th, I generated high-resolution water column profiles of particulate organic carbon flux to constrain carbon regeneration lengthscales in both oligotrophic and oxygen minimum zone settings. In chapter 4, I demonstrate the importance of isopycnal mixing in transporting 230Th, 231Pa, and 232Th into the Pacific Southern Ocean, showing the first high-resolution dissolved Th and Pa data from the region.
Chapter 5 provides estimates of dust input spanning the South Pacific using two methods based on paired 230Th-232Th, evaluates the flux of dust-borne iron, and discusses the impacts on measured and modeled nitrogen fixation rates in the South Pacific gyre. Finally, in chapter 6 I present enigmatic profiles of Th and Pa isotopes from the semi-enclosed Peru and Bauer Basins, with anomalous Th and Pa removal extending 1-2km above the seafloor. I hypothesize that these depletions are related to the extent of water mass contact the seafloor, allowing for scavenging removal of Th and Pa by resuspended sediments
²³⁰Th normalization: New insights on an essential tool for quantifying sedimentary fluxes in the modern and Quaternary ocean
²³⁰Th‐normalization is a valuable paleoceanographic tool for reconstructing high‐resolution sediment fluxes during the late Pleistocene (last ~500,000 years). As its application has expanded to ever more diverse marine environments, the nuances of ²³⁰Th systematics, with regards to particle type, particle size, lateral advective/diffusive redistribution, and other processes, have emerged. We synthesized over 1000 sedimentary records of ²³⁰Th from across the global ocean at two time slices, the Late Holocene (0‐5000 years ago, or 0‐5 ka) and the Last Glacial Maximum (18.5‐23.5 ka), and investigated the spatial structure of ²³⁰Th‐normalized mass fluxes. On a global scale, sedimentary mass fluxes were significantly higher during the Last Glacial Maximum (1.79‐2.17 g/cm²kyr, 95% confidence) relative to the Holocene (1.48‐1.68 g/cm²kyr, 95% confidence). We then examined the potential confounding influences of boundary scavenging, nepheloid layers, hydrothermal scavenging, size dependent sediment fractionation, and carbonate dissolution on the efficacy of ²³⁰Th as a constant flux proxy. Anomalous ²³⁰Th behavior is sometimes observed proximal to hydrothermal ridges and in continental margins where high particle fluxes and steep continental slopes can lead to the combined effects of boundary scavenging and nepheloid interference. Notwithstanding these limitations, we found that ²³⁰Th‐normalization is a robust tool for determining sediment mass accumulation rates in the majority of pelagic marine settings (> 1000 m water depth)
Atmospheric Dust Inputs, Iron Cycling, and Biogeochemical Connections in the South Pacific Ocean from Thorium Isotopes
One of the primary sources of micronutrients to the sea surface in remote ocean regions is the deposition of atmospheric dust. Geographic patterns in biogeochemical processes such as primary production and nitrogen fixation that require micronutrients like iron (Fe) are modulated in part by the spatial distribution of dust supply. Global models of dust deposition rates are poorly calibrated in the open ocean, owing to the difficulty of determining dust fluxes in sparsely sampled regions. We present new estimates of dust and Fe input rates from measurements of dissolved and particulate thorium isotopes ²³⁰Th and ²³²Th on the FS Sonne SO245 section (GEOTRACES process study GPpr09) in the South Pacific. We first discuss high‐resolution upper water column profiles of Th isotopes and the implications for the systematics of dust flux reconstructions from seawater Th measurements. We find dust fluxes in the center of the highly oligotrophic South Pacific Gyre that are the lowest of any mean annual dust input rates measured in the global oceans, but that are 1–2 orders of magnitude higher than those estimated by global dust models. We also determine dust‐borne Fe fluxes and reassess the importance of individual Fe sources to the surface South Pacific Gyre, finding that dust dissolution, not vertical or lateral diffusion, is the primary Fe source. Finally, we combine our estimates of Fe flux in dust with previously published cellular and enzymatic quotas to determine theoretical upper limits on annual average nitrogen fixation rates for a given Fe deposition rate
Atmospheric Dust Inputs, Iron Cycling, and Biogeochemical Connections in the South Pacific Ocean from Thorium Isotopes
One of the primary sources of micronutrients to the sea surface in remote ocean regions is the deposition of atmospheric dust. Geographic patterns in biogeochemical processes such as primary production and nitrogen fixation that require micronutrients like iron (Fe) are modulated in part by the spatial distribution of dust supply. Global models of dust deposition rates are poorly calibrated in the open ocean, owing to the difficulty of determining dust fluxes in sparsely sampled regions. We present new estimates of dust and Fe input rates from measurements of dissolved and particulate thorium isotopes ²³⁰Th and ²³²Th on the FS Sonne SO245 section (GEOTRACES process study GPpr09) in the South Pacific. We first discuss high‐resolution upper water column profiles of Th isotopes and the implications for the systematics of dust flux reconstructions from seawater Th measurements. We find dust fluxes in the center of the highly oligotrophic South Pacific Gyre that are the lowest of any mean annual dust input rates measured in the global oceans, but that are 1–2 orders of magnitude higher than those estimated by global dust models. We also determine dust‐borne Fe fluxes and reassess the importance of individual Fe sources to the surface South Pacific Gyre, finding that dust dissolution, not vertical or lateral diffusion, is the primary Fe source. Finally, we combine our estimates of Fe flux in dust with previously published cellular and enzymatic quotas to determine theoretical upper limits on annual average nitrogen fixation rates for a given Fe deposition rate
230Th Normalization: New Insights on an Essential Tool for Quantifying Sedimentary Fluxes in the Modern and Quaternary Ocean
230Th normalization is a valuable paleoceanographic tool for reconstructing high-resolution sediment fluxes during the late Pleistocene (last ~500,000 years). As its application has expanded to ever more diverse marine environments, the nuances of 230Th systematics, with regard to particle type, particle size, lateral advective/diffusive redistribution, and other processes, have emerged. We synthesized over 1000 sedimentary records of 230Th from across the global ocean at two time slices, the late Holocene (0–5,000 years ago, or 0–5 ka) and the Last Glacial Maximum (18.5–23.5 ka), and investigated the spatial structure of 230Th-normalized mass fluxes. On a global scale, sedimentary mass fluxes were significantly higher during the Last Glacial Maximum (1.79–2.17 g/cm2kyr, 95% confidence) relative to the Holocene (1.48–1.68 g/cm2kyr, 95% confidence). We then examined the potential confounding influences of boundary scavenging, nepheloid layers, hydrothermal scavenging, size-dependent sediment fractionation, and carbonate dissolution on the efficacy of 230Th as a constant flux proxy. Anomalous 230Th behavior is sometimes observed proximal to hydrothermal ridges and in continental margins where high particle fluxes and steep continental slopes can lead to the combined effects of boundary scavenging and nepheloid interference. Notwithstanding these limitations, we found that 230Th normalization is a robust tool for determining sediment mass accumulation rates in the majority of pelagic marine settings (\u3e1,000 m water depth)
Dissolved and particulate barium distributions along the US GEOTRACES North Atlantic and East Pacific zonal transects (GA03 and GP16): global implications for the marine barium cycle
Author Posting. © American Geophysical Union, 2022. 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 36(6), (2022): e2022GB007330, https://doi.org/10.1029/2022gb007330.Processes controlling dissolved barium (dBa) were investigated along the GEOTRACES GA03 North Atlantic and GP16 Eastern Tropical Pacific transects, which traversed similar physical and biogeochemical provinces. Dissolved Ba concentrations are lowest in surface waters (∼35–50 nmol kg−1) and increase to 70–80 and 140–150 nmol kg−1 in deep waters of the Atlantic and Pacific transects, respectively. Using water mass mixing models, we estimate conservative mixing that accounts for most of dBa variability in both transects. To examine nonconservative processes, particulate excess Ba (pBaxs) formation and dissolution rates were tracked by normalizing particulate excess 230Th activities. Th-normalized pBaxs fluxes, with barite as the likely phase, have subsurface maxima in the top 1,000 m (∼100–200 μmol m−2 year−1 average) in both basins. Barite precipitation depletes dBa within oxygen minimum zones from concentrations predicted by water mass mixing, whereas inputs from continental margins, particle dissolution in the water column, and benthic diffusive flux raise dBa above predications. Average pBaxs burial efficiencies along GA03 and GP16 are ∼37% and 17%–100%, respectively, and do not seem to be predicated on barite saturation indices in the overlying water column. Using published values, we reevaluate the global freshwater dBa river input as 6.6 ± 3.9 Gmol year−1. Estuarine mixing processes may add another 3–13 Gmol year−1. Dissolved Ba inputs from broad shallow continental margins, previously unaccounted for in global marine summaries, are substantial (∼17 Gmol year−1), exceeding terrestrial freshwater inputs. Revising river and shelf dBa inputs may help bring the marine Ba isotope budget more into balance.The International GEOTRACES Programme is possible in part thanks to the support from the U.S. National Science Foundation (Grant OCE-1840868) to the Scientific Committee on Oceanic Research (SCOR). This research was supported by the National Science Foundation under Grant No. NSF OCE-0927951, NSF OCE-1137851, NSF OCE-1261214, and NSF OCE-1925503 to A. M. Shiller; NSF OCE-1829563 to R. F. Anderson; NSF OCE-0927064 and NSF OCE-1233688 to R. F. Anderson and M. Q. Fleisher; NSF OCE-0927754 to R. Lawrence Edwards; NSF OCE-1233903 to R. Lawrence Edwards and H. Cheng; NSF OCE-0926860 to L. F. Robinson; NSF OCE-0963026 and NSF OCE-1518110 to P. J. Lam; and NSF OCE-1232814 to B. S. Twining
230 Th normalization: new insights on an essential tool for quantifying sedimentary fluxes in the modern and quaternary ocean
© The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Costa, K. M., Hayes, C. T., Anderson, R. F., Pavia, F. J., Bausch, A., Deng, F., Dutay, J., Geibert, W., Heinze, C., Henderson, G., Hillaire-Marcel, C., Hoffmann, S., Jaccard, S. L., Jacobel, A. W., Kienast, S. S., Kipp, L., Lerner, P., Lippold, J., Lund, D., Marcantonio, F., McGee, D., McManus, J. F., Mekik, F., Middleton, J. L., Missiaen, L., Not, C., Pichat, S., Robinson, L. F., Rowland, G. H., Roy-Barman, M., Alessandro, Torfstein, A., Winckler, G., & Zhou, Y. 230 Th normalization: new insights on an essential tool for quantifying sedimentary fluxes in the modern and quaternary ocean. Paleoceanography and Paleoclimatology, 35(2), (2020): e2019PA003820, doi:10.1029/2019PA003820.230Th normalization is a valuable paleoceanographic tool for reconstructing high‐resolution sediment fluxes during the late Pleistocene (last ~500,000 years). As its application has expanded to ever more diverse marine environments, the nuances of 230Th systematics, with regard to particle type, particle size, lateral advective/diffusive redistribution, and other processes, have emerged. We synthesized over 1000 sedimentary records of 230Th from across the global ocean at two time slices, the late Holocene (0–5,000 years ago, or 0–5 ka) and the Last Glacial Maximum (18.5–23.5 ka), and investigated the spatial structure of 230Th‐normalized mass fluxes. On a global scale, sedimentary mass fluxes were significantly higher during the Last Glacial Maximum (1.79–2.17 g/cm2kyr, 95% confidence) relative to the Holocene (1.48–1.68 g/cm2kyr, 95% confidence). We then examined the potential confounding influences of boundary scavenging, nepheloid layers, hydrothermal scavenging, size‐dependent sediment fractionation, and carbonate dissolution on the efficacy of 230Th as a constant flux proxy. Anomalous 230Th behavior is sometimes observed proximal to hydrothermal ridges and in continental margins where high particle fluxes and steep continental slopes can lead to the combined effects of boundary scavenging and nepheloid interference. Notwithstanding these limitations, we found that 230Th normalization is a robust tool for determining sediment mass accumulation rates in the majority of pelagic marine settings (>1,000 m water depth).We thank Zanna Chase and one anonymous reviewer for valuable feedback. K. M. C. was supported by a Postdoctoral Scholarship at WHOI. L. M. acknowledges funding from the Australian Research Council grant DP180100048. The contribution of C. T. H., J. F. M., and R. F. A. were supported in part by the U.S. National Science Foundation (US‐NSF). G. H. R. was supported by the Natural Environment Research Council (grant NE/L002434/1). S. L. J. acknowledges support from the Swiss National Science Foundation (grants PP002P2_144811 and PP00P2_172915). This study was supported by the Past Global Changes (PAGES) project, which in turn received support from the Swiss Academy of Sciences and the US‐NSF. This work grew out of a 2018 workshop in Aix‐Marseille, France, funded by PAGES, GEOTRACES, SCOR, US‐NSF, Aix‐Marseille Université, and John Cantle Scientific. All data are publicly available as supporting information to this document and on the National Center for Environmental Information (NCEI) at https://www.ncdc.noaa.gov/paleo/study/28791
- …