Byrne Robert H.

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Byrne
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Robert H.
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  • Article
    The marine inorganic carbon system along the Gulf of Mexico and Atlantic coasts of the United States : insights from a transregional coastal carbon study
    (Association for the Sciences of Limnology and Oceanography, 2013-01) Wang, Zhaohui Aleck ; Wanninkhof, Rik ; Cai, Wei-Jun ; Byrne, Robert H. ; Hu, Xinping ; Peng, Tsung-Hung ; Huang, Wei-Jen
    Distributions of total alkalinity (TA), dissolved inorganic carbon (DIC), and other parameters relevant to the marine inorganic carbon system were investigated in shelf and adjacent ocean waters during a U.S. Gulf of Mexico and East Coast Carbon cruise in July–August 2007. TA exhibited near-conservative behavior with respect to salinity. Shelf concentrations were generally high in southern waters (Gulf of Mexico and East Florida) and decreased northward from Georgia to the Gulf of Maine. DIC was less variable geographically and exhibited strongly nonconservative behavior. As a result, the ratio of TA to DIC generally decreased northward. The spatial patterns of other CO2 system parameters closely followed those of the TA : DIC ratio. All sampled shelf waters were supersaturated with respect to aragonite (saturation state ΩA > 1). The most intensely buffered and supersaturated waters (ΩA > 5.0) were in northern Gulf of Mexico river-plume waters; the least intensely buffered and least supersaturated waters (ΩA < 1.3) were in the deep Gulf of Maine. Due to their relatively low pH, ΩA, and buffer intensity, waters of the northeastern U.S. shelves may be more susceptible to acidification pressures than are their southern counterparts. In the Mid-Atlantic Bight, alongshore mixing tended to increase DIC concentrations southward, but this effect was largely offset by the opposing effects of biogeochemical processing. In the Gulf of Mexico, downstream increases in Loop Current DIC suggested significant contributions from shelf and gulf waters, estimated at 9.1 × 109 mol C d−1. Off the southeastern U.S., along-flow chemical changes in the Florida Current were dominated by mixing associated with North Atlantic subtropical recirculation.
  • Article
    Shallow calcium carbonate cycling in the North Pacific Ocean
    (American Geophysical Union, 2022-05-06) Subhas, Adam V. ; Dong, Sijia ; Naviaux, John D. ; Rollins, Nick E. ; Ziveri, Patrizia ; Gray, William R. ; Rae, James W. B. ; Liu, Xuewu ; Byrne, Robert H. ; Chen, Sang ; Moore, Christopher ; Martell-Bonet, Loraine ; Steiner, Zvi ; Antler, Gilad ; Hu, Huanting ; Lunstrum, Abby ; Hou, Yi ; Kemnitz, Nathaniel ; Stutsman, Johnny ; Pallacks, Sven ; Dugenne, Mathilde ; Quay, Paul D. ; Berelson, William M. ; Adkins, Jess F.
    The cycling of biologically produced calcium carbonate (CaCO3) in the ocean is a fundamental component of the global carbon cycle. Here, we present experimental determinations of in situ coccolith and foraminiferal calcite dissolution rates. We combine these rates with solid phase fluxes, dissolved tracers, and historical data to constrain the alkalinity cycle in the shallow North Pacific Ocean. The in situ dissolution rates of coccolithophores demonstrate a nonlinear dependence on saturation state. Dissolution rates of all three major calcifying groups (coccoliths, foraminifera, and aragonitic pteropods) are too slow to explain the patterns of both CaCO3 sinking flux and alkalinity regeneration in the North Pacific. Using a combination of dissolved and solid-phase tracers, we document a significant dissolution signal in seawater supersaturated for calcite. Driving CaCO3 dissolution with a combination of ambient saturation state and oxygen consumption simultaneously explains solid-phase CaCO3 flux profiles and patterns of alkalinity regeneration across the entire N. Pacific basin. We do not need to invoke the presence of carbonate phases with higher solubilities. Instead, biomineralization and metabolic processes intimately associate the acid (CO2) and the base (CaCO3) in the same particles, driving the coupled shallow remineralization of organic carbon and CaCO3. The linkage of these processes likely occurs through a combination of dissolution due to zooplankton grazing and microbial aerobic respiration within degrading particle aggregates. The coupling of these cycles acts as a major filter on the export of both organic and inorganic carbon to the deep ocean.
  • Article
    Best practice data standards for discrete chemical oceanographic observations
    (Frontiers Media, 2022-01-21) Jiang, Li-Qing ; Pierrot, Denis ; Wanninkhof, Rik ; Feely, Richard A. ; Tilbrook, Bronte ; Alin, Simone R. ; Barbero, Leticia ; Byrne, Robert H. ; Carter, Brendan ; Dickson, Andrew G. ; Gattuso, Jean-Pierre ; Greeley, Dana ; Hoppema, Mario ; Humphreys, Matthew P. ; Karstensen, Johannes ; Lange, Nico ; Lauvset, Siv K. ; Lewis, Ernie R. ; Olsen, Are ; Perez, Fiz F. ; Sabine, Christopher ; Sharp, Jonathan D. ; Tanhua, Toste ; Trull, Thomas W. ; Velo, Anton ; Allegra, Andrew J. ; Barker, Paul M. ; Burger, Eugene ; Cai, Wei-Jun ; Chen, Chen-Tung A. ; Cross, Jessica N. ; Garcia, Hernan E. ; Hernandez-Ayon, Jose Martin ; Hu, Xinping ; Kozyr, Alex ; Langdon, Chris ; Lee, Kitack ; Salisbury, Joseph E. ; Wang, Zhaohui Aleck ; Xue, Liang
    Effective data management plays a key role in oceanographic research as cruise-based data, collected from different laboratories and expeditions, are commonly compiled to investigate regional to global oceanographic processes. Here we describe new and updated best practice data standards for discrete chemical oceanographic observations, specifically those dealing with column header abbreviations, quality control flags, missing value indicators, and standardized calculation of certain properties. These data standards have been developed with the goals of improving the current practices of the scientific community and promoting their international usage. These guidelines are intended to standardize data files for data sharing and submission into permanent archives. They will facilitate future quality control and synthesis efforts and lead to better data interpretation. In turn, this will promote research in ocean biogeochemistry, such as studies of carbon cycling and ocean acidification, on regional to global scales. These best practice standards are not mandatory. Agencies, institutes, universities, or research vessels can continue using different data standards if it is important for them to maintain historical consistency. However, it is hoped that they will be adopted as widely as possible to facilitate consistency and to achieve the goals stated above.
  • Article
    Storm-induced upwelling of high pCO2 waters onto the continental shelf of the western Arctic Ocean and implications for carbonate mineral saturation states
    (American Geophysical Union, 2012-04-11) Mathis, Jeremy T. ; Pickart, Robert S. ; Byrne, Robert H. ; McNeil, Craig L. ; Moore, G. W. K. ; Juranek, Laurie W. ; Liu, Xuewu ; Ma, Jian ; Easley, Regina A. ; Elliot, Matthew M. ; Cross, Jessica N. ; Reisdorph, Stacey C. ; Bahr, Frank B. ; Morison, James H. ; Lichendorf, Trina ; Feely, Richard A.
    The carbon system of the western Arctic Ocean is undergoing a rapid transition as sea ice extent and thickness decline. These processes are dynamically forcing the region, with unknown consequences for CO2 fluxes and carbonate mineral saturation states, particularly in the coastal regions where sensitive ecosystems are already under threat from multiple stressors. In October 2011, persistent wind-driven upwelling occurred in open water along the continental shelf of the Beaufort Sea in the western Arctic Ocean. During this time, cold (<−1.2°C), salty (>32.4) halocline water—supersaturated with respect to atmospheric CO2 (pCO2 > 550 μatm) and undersaturated in aragonite (Ωaragonite < 1.0) was transported onto the Beaufort shelf. A single 10-day event led to the outgassing of 0.18–0.54 Tg-C and caused aragonite undersaturations throughout the water column over the shelf. If we assume a conservative estimate of four such upwelling events each year, then the annual flux to the atmosphere would be 0.72–2.16 Tg-C, which is approximately the total annual sink of CO2 in the Beaufort Sea from primary production. Although a natural process, these upwelling events have likely been exacerbated in recent years by declining sea ice cover and changing atmospheric conditions in the region, and could have significant impacts on regional carbon budgets. As sea ice retreat continues and storms increase in frequency and intensity, further outgassing events and the expansion of waters that are undersaturated in carbonate minerals over the shelf are probable.
  • Article
    Uncertainty sources for measurable ocean carbonate chemistry variables
    (Association for the Sciences of Limnology and Oceanography (ASLO), 2023-12-14) Carter, Brendan R. ; Sharp, Jonathan D. ; Dickson, Andrew G. ; Alvarez, Marta ; Fong, Michael B. ; Garcia-Ibanez, Maribel I. ; Woosley, Ryan J. ; Takeshita, Yuichiro ; Barbero, Leticia ; Byrne, Robert H. ; Cai, Wei-Jun ; Chierici, Melissa ; Clegg, Simon L. ; Easley, Regina A. ; Fassbender, Andrea J. ; Fleger, Kalla L. ; Li, Xinyu ; Martin-Mayor, Macarena ; Schockman, Katelyn M. ; Wang, Zhaohui Aleck
    The ocean carbonate system is critical to monitor because it plays a major role in regulating Earth's climate and marine ecosystems. It is monitored using a variety of measurements, and it is commonly understood that all components of seawater carbonate chemistry can be calculated when at least two carbonate system variables are measured. However, several recent studies have highlighted systematic discrepancies between calculated and directly measured carbonate chemistry variables and these discrepancies have large implications for efforts to measure and quantify the changing ocean carbon cycle. Given this, the Ocean Carbonate System Intercomparison Forum (OCSIF) was formed as a working group through the Ocean Carbon and Biogeochemistry program to coordinate and recommend research to quantify and/or reduce uncertainties and disagreements in measurable seawater carbonate system measurements and calculations, identify unknown or overlooked sources of these uncertainties, and provide recommendations for making progress on community efforts despite these uncertainties. With this paper we aim to (1) summarize recent progress toward quantifying and reducing carbonate system uncertainties; (2) advocate for research to further reduce and better quantify carbonate system measurement uncertainties; (3) present a small amount of new data, metadata, and analysis related to uncertainties in carbonate system measurements; and (4) restate and explain the rationales behind several OCSIF recommendations. We focus on open ocean carbonate chemistry, and caution that the considerations we discuss become further complicated in coastal, estuarine, and sedimentary environments.