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  1. Abstract

    Fully and accurately reconstructing changes in oceanic productivity and carbon export and their controls is critical to determining the efficiency of the biological pump and its role in the global carbon cycle through time, particularly in modern CO2source regions like the eastern equatorial Pacific (EEP). Here we present new high-resolution records of sedimentary230Th-normalized opal and nannofossil carbonate fluxes and [231Pa/230Th]xs ratios from site MV1014-02-17JC in the Panama Basin. We find that, across the last deglaciation, phytoplankton community structure is driven by changing patterns of nutrient (nitrate, iron, and silica) availability which, in turn, are caused by variability in the position of the Intertropical Convergence Zone (ITCZ) and associated changes in biogeochemical cycling and circulation in the Southern Ocean. Our multi-proxy work suggests greater scrutiny is required in the interpretation of common geochemical proxies of productivity and carbon export in the EEP.

     
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  2. Abstract

    North African dust is known to be deposited in the Gulf of Mexico, but its deposition rate and associated supply of lithogenic dissolved metals, such as the abiotic metal thorium or the micronutrient metal iron, have not been well‐quantified.232Th is an isotope with similar sources as iron and its input can be quantified using radiogenic230Th. By comparing dissolved232Th fluxes at three sites in the northern Gulf of Mexico with upwind sites in the North Atlantic, we place an upper bound on North African dust contributions to232Th and Fe in the Gulf of Mexico, which is about 30% of the total input. Precision on this bound is hindered by uncertainty in the relative rates of dust deposition in the North Atlantic and the northern Gulf of Mexico. Based on available radium data, shelf sources, including rivers, submarine groundwater discharge, and benthic sedimentary releases are likely as important if not more important than dust in the budget of lithogenic metals in the Gulf of Mexico. In other words, it is likely there is no one dominant source of Th and Fe in the Gulf of Mexico. Finally, our estimated Fe input in the northern Gulf of Mexico implies an Fe residence time of less than 6 months, similar to that in the North Atlantic despite significantly higher supply rates in the Gulf of Mexico.

     
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  3. Abstract

    We compile full ocean‐depth size‐fractionated (1–51 and >51 μm) particle concentration and composition of suspended particulate matter from three recent U.S. GEOTRACES cruises, and exploit detailed information of particle characteristics measured to give insights into controls on sinking velocity and mass flux. Our model integrates the concept of fractal scaling into Stokes' Law by incorporating one of two porosity‐size power law relationships that result in fractal dimensions of 1.4 and 2.1. The medians of pump‐derived total (>1 μm) mass flux in the upper 100 m of gyre stations are 285.1, 609.2, and 99.3 mg/m2/d in the North Atlantic, Eastern Tropical South Pacific, and Western Arctic Ocean cruises, respectively. In this data set, variations in particle concentration were generally more important than sinking velocity in controlling variations in mass flux. We examine different terms in a Stokes' Law model to explore how variations in particle and water column characteristics from these three cruises affect mass flux. The decomposition of different aspects of the Stokes' relationship sheds light on the lowest total mass flux of the three cruises in the Western Arctic, which could be explained by the Arctic having the lowest particle concentrations as well as the lowest sinking velocities due to having the smallest particle sizes and the most viscous water. This work shows the importance of both particle characteristics and size distribution for mass fluxes, and similar methods can be applied to existing and future size‐fractionated filtered particulate measurements to improve our understanding of the biological pump elsewhere.

     
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  4. Abstract

    Coastal ecosystems are highly dynamic areas for carbon cycling and are likely to be negatively impacted by increasing ocean acidification. This research focused on dissolved inorganic carbon (DIC) and total alkalinity (TA) in the Mississippi Sound to understand the influence of local rivers on coastal acidification. This area receives large fluxes of freshwater from local rivers, in addition to episodic inputs from the Mississippi River through a human‐built diversion, the Bonnet Carré Spillway. Sites in the Sound were sampled monthly from August 2018 to November 2019 and weekly from June to August 2019 in response to an extended spillway opening. Prior to the 2019 spillway opening, the contribution of the local, lower alkalinity rivers to the Sound may have left the study area more susceptible to coastal acidification during winter months, with aragonite saturation states (Ωar) < 2. After the spillway opened, despite a large increase in TA throughout the Sound, aragonite saturation states remained low, likely due to hypoxia and increased CO2concentrations in subsurface waters. Increased Mississippi River input could represent a new normal in the Sound's hydrography during spring and summer months. The spillway has been utilized more frequently over the last two decades due to increasing precipitation in the Mississippi River watershed, which is primarily associated with climate change. Future increases in freshwater discharge and the associated declines in salinity, dissolved oxygen, and Ωarin the Sound will likely be detrimental to oyster stocks and the resilience of similar ecosystems to coastal acidification.

     
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  5. null (Ed.)
  6. Abstract

    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−1in 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 excess230Th activities. Th‐normalized pBaxsfluxes, with barite as the likely phase, have subsurface maxima in the top 1,000 m (∼100–200 μmol m−2 year−1average) 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 pBaxsburial 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.

     
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  7. Abstract

    Ocean time‐series sites are influenced by both temporal variability, as in situ conditions change, as well as spatial variability, as water masses move across the fixed observation point. To remove the effect of spatial variability, this study made sub‐daily Lagrangian observations of trace elements and isotopes (Al, Sc, Mn, Fe, Co, Ni, Cu, Zn, Cd, Pb,232Th, and230Th) in surface water over a 12‐day period (July–August 2015) in the North Pacific near the Hawaii Ocean Time‐series Station ALOHA. Additionally, a vertical profile in the upper 250 m was analyzed. This dataset is intercalibrated with GEOTRACES standards and provides a consistent baseline for trace element studies in the oligotrophic North Pacific. No diel changes in trace elements could be resolved, although day‐to‐day variations were resolved for some elements (Fe, Cu, and Zn), which may be related to organic matter cycling or ligand availability. Pb concentrations remained relatively constant during 1997–2015, presenting a change from previous decreases. Nutrient to trace element stoichiometric ratios were compared to those observed in phytoplankton as an indication of the extent of biological trace element utilization in this ecosystem, providing a basis for future ecological trace element studies.

     
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