21 research outputs found

    Influence of biological carbon export on ocean carbon uptake over the annual cycle across the North Pacific Ocean

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    Author Posting. © American Geophysical Union, 2017. 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 31 (2017): 81–95, doi:10.1002/2016GB005527.We evaluate the influences of biological carbon export, physical circulation, and temperature-driven solubility changes on air-sea CO2 flux across the North Pacific basin (35°N–50°N, 142°E–125°W) throughout the full annual cycle by constructing mixed layer budgets for dissolved inorganic carbon (DIC) and pCO2, determined on 15 container ship transects between Hong Kong and Long Beach, CA, from 2008 to 2012. Annual air-sea CO2 flux is greatest in the western North Pacific and decreases eastward across the basin (2.7 ± 0.9 mol C m−2 yr−1 west of 170°E, as compared to 2.1 ± 0.3 mol C m−2 yr−1 east of 160°W). East of 160°W, DIC removal by annual net community production (NCP) more than fully offsets the DIC increase due to air-sea CO2 flux. However, in the region west of 170°E influenced by deep winter mixing, annual NCP only offsets ~20% of the DIC increase due to air-sea CO2 flux, requiring significant DIC removal by geostrophic advection. Temperature-driven solubility changes have no net influence on pCO2 and account for <25% of annual CO2 uptake. The seasonal timing of NCP strongly affects its influence on air-sea CO2 flux. Biological carbon export from the mixed layer has a stronger influence on pCO2 in summer when mixed layers are shallow, but changes in pCO2 have a stronger influence on air-sea CO2 flux in winter when high wind speeds drive more vigorous gas exchange. Thus, it is necessary to determine the seasonal timing as well as the annual magnitude of NCP to determine its influence on ocean carbon uptake.NDSEG Fellowship from the Office of Naval Research; NSF Graduate Research Fellowship; NSF Ocean Sciences Grant Numbers: 0628663, 1259055; NOAA Climate Program Office Grant Number: A10OAR43100882017-07-2

    The North Atlantic biological pump : insights from the Ocean Observatories Initiative Irminger Sea Array

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    Author Posting. © The Oceanography Society, 2018. This article is posted here by permission of The Oceanography Society for personal use, not for redistribution. The definitive version was published in Oceanography 31, no. 1 (2018): 42–49, doi:10.5670/oceanog.2018.108.The biological pump plays a key role in the global carbon cycle by transporting photosynthetically fixed organic carbon into the deep ocean, where it can be sequestered from the atmosphere over annual or longer time scales if exported below the winter ventilation depth. In the subpolar North Atlantic, carbon sequestration via the biological pump is influenced by two competing forces: a spring diatom bloom that features large, fast-sinking biogenic particles, and deep winter mixing that requires particles to sink much further than in other ocean regions to escape winter ventilation. We synthesize biogeochemical sensor data from the first two years of operations at the Ocean Observatories Initiative Irminger Sea Array of moorings and gliders (September 2014–July 2016), providing the first simultaneous year-round observations of biological carbon cycling processes in both the surface ocean and the seasonal thermocline in this critical but previously undersampled region. These data show significant mixed layer net autotrophy during the spring bloom and significant respiration in the seasonal thermocline during the stratified season (~5.9 mol C m–2 remineralized between 200 m and 1,000 m). This respired carbon is subsequently ventilated during winter convective mixing (>1,000 m), a significant reduction in potential carbon sequestration. This highlights the importance of year-round observations to accurately constrain the biological pump in the subpolar North Atlantic, as well as other high-latitude regions that experience deep winter mixing.Hilary Palevsky acknowledges support from the Postdoctoral Scholar Program at the Woods Hole Oceanographic Institution, with funding provided by the Weston Howland Jr. Postdoctoral Scholarship

    How choice of depth horizon influences the estimated spatial patterns and global magnitude of ocean carbon export flux

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    Author Posting. © American Geophysical Union, 2018. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 45 (2018): 4171-4179, doi:10.1029/2017GL076498.Estimated rates and efficiency of ocean carbon export flux are sensitive to differences in the depth horizons used to define export, which often vary across methodological approaches. We evaluate sinking particulate organic carbon (POC) flux rates and efficiency (e‐ratios) in a global earth system model, using a range of commonly used depth horizons: the seasonal mixed layer depth, the particle compensation depth, the base of the euphotic zone, a fixed depth horizon of 100 m, and the maximum annual mixed layer depth. Within this single dynamically consistent model framework, global POC flux rates vary by 30% and global e‐ratios by 21% across different depth horizon choices. Zonal variability in POC flux and e‐ratio also depends on the export depth horizon due to pronounced influence of deep winter mixing in subpolar regions. Efforts to reconcile conflicting estimates of export need to account for these systematic discrepancies created by differing depth horizon choices.Woods Hole Oceanographic Institution (WHOI); National Science Foundation Grant Number: OCE‐14340002018-10-2

    Discrepant estimates of primary and export production from satellite algorithms, a biogeochemical model, and geochemical tracer measurements in the North Pacific Ocean

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    Author Posting. © American Geophysical Union, 2016. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 43 (2016): 8645–8653, doi:10.1002/2016GL070226.Estimates of primary and export production (PP and EP) based on satellite remote sensing algorithms and global biogeochemical models are widely used to provide year-round global coverage not available from direct observations. However, observational data to validate these approaches are limited. We find that no single satellite algorithm or model can reproduce seasonal and annual geochemically determined PP, export efficiency (EP/PP), and EP rates throughout the North Pacific basin, based on comparisons throughout the full annual cycle at time series stations in the subarctic and subtropical gyres and basin-wide regions sampled by container ship transects. The high-latitude regions show large PP discrepancies in winter and spring and strong effects of deep winter mixed layers on annual EP that cannot be accounted for in current satellite-based approaches. These results underscore the need to evaluate satellite- and model-based estimates using multiple productivity parameters measured over broad ocean regions throughout the annual cycle.NDSEG Fellowship from the Office of Naval Research; NSF Graduate Research Fellowship; ARCS Foundation Fellowship2017-02-2

    Synoptic Mesoscale to Basin Scale Variability in Biological Productivity and Chlorophyll in the Kuroshio Extension Region

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    The Kuroshio current separates from the Japanese coast to become the eastward flowing Kuroshio Extension (KE) characterized by a strong latitudinal density front, high levels of mesoscale (eddy) energy, and high chlorophyll a (Chl). While satellite measurements of Chl show evidence of the impact of mesoscale eddies on the standing stock of phytoplankton, there have been very limited synoptic, spatially resolved in situ estimates of productivity in this region. Here, we present underway measurements of oxygen/argon supersaturation (ΔO2/Ar), a tracer of net biological productivity, for the KE made in spring, summer, and early autumn. We find large seasonal differences in the relationships between ΔO2/Ar, Chl, and sea level anomaly (SLA), a proxy for local thermocline depth deviations driven by mesoscale eddies derived from satellite observations. We show that the KE is a pronounced hotspot of high ΔO2/Ar in spring, but corresponding surface Chl values are low and have no correlation with ΔO2/Ar. In summer, there is a hotspot of productivity associated with the Oyashio front, where ΔO2/Ar and Chl are strongly positively correlated. In autumn, ΔO2/Ar and Chl are consistently low throughout the region and also positively correlated. By combining our analysis of the in situ ΔO2/Ar data with complementary Argo, BGC-Argo, repeat hydrography, and SLA observations, we infer the combination of physical and biological controls that drive the observed distributions of ΔO2/Ar and Chl. We find that the KE and Oyashio currents both act to supply nutrients laterally, fueling regions of high productivity in spring and summer, respectively

    Seasonal asymmetry in the evolution of surface ocean pCO2 and pH thermodynamic drivers and the influence on sea‐air CO2 flux

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    © The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Global Biogeochemical Cycles 32 (2018): 1476-1497, doi:10.1029/2017GB005855.It has become clear that anthropogenic carbon invasion into the surface ocean drives changes in the seasonal cycles of carbon dioxide partial pressure (pCO2) and pH. However, it is not yet known whether the resulting sea‐air CO2 fluxes are symmetric in their seasonal expression. Here we consider a novel application of observational constraints and modeling inferences to test the hypothesis that changes in the ocean's Revelle factor facilitate a seasonally asymmetric response in pCO2 and the sea‐air CO2 flux. We use an analytical framework that builds on observed sea surface pCO2 variability for the modern era and incorporates transient dissolved inorganic carbon concentrations from an Earth system model. Our findings reveal asymmetric amplification of pCO2 and pH seasonal cycles by a factor of two (or more) above preindustrial levels under Representative Concentration Pathway 8.5. These changes are significantly larger than observed modes of interannual variability and are relevant to climate feedbacks associated with Revelle factor perturbations. Notably, this response occurs in the absence of changes to the seasonal cycle amplitudes of dissolved inorganic carbon, total alkalinity, salinity, and temperature, indicating that significant alteration of surface pCO2 can occur without modifying the physical or biological ocean state. This result challenges the historical paradigm that if the same amount of carbon and nutrients is entrained and subsequently exported, there is no impact on anthropogenic carbon uptake. Anticipation of seasonal asymmetries in the sea surface pCO2 and CO2 flux response to ocean carbon uptake over the 21st century may have important implications for carbon cycle feedbacks.Cooperative Institute for Climate Science Grant Number: NA17RJ2612; David and Lucile Packard Foundation/MBARI Grant Number: 4696; NOAA Office of Climate Observations Grant Number: NA11OAR4310066; NOAA. Grant Number NA11OAR4310066; KBR Grant Numbers: A08OAR4320752, NA17RJ261

    The annual cycle of gross primary production, net community production, and export efficiency across the North Pacific Ocean

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    Author Posting. © American Geophysical Union, 2016. 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 30 (2016): 361–380, doi:10.1002/2015GB005318.We measured triple oxygen isotopes and oxygen/argon dissolved gas ratios as nonincubation-based geochemical tracers of gross oxygen production (GOP) and net community production (NCP) on 16 container ship transects across the North Pacific from 2008 to 2012. We estimate rates and efficiency of biological carbon export throughout the full annual cycle across the North Pacific basin (35°N–50°N, 142°E–125°W) by constructing mixed layer budgets that account for physical and biological influences on these tracers. During the productive season from spring to fall, GOP and NCP are highest in the Kuroshio region west of 170°E and decrease eastward across the basin. However, deep winter mixed layers (>200 m) west of 160°W ventilate ~40–90% of this seasonally exported carbon, while only ~10% of seasonally exported carbon east of 160°W is ventilated in winter where mixed layers are <120 m. As a result, despite higher annual GOP in the west than the east, the annual carbon export (sequestration) rate and efficiency decrease westward across the basin from export of 2.3 ± 0.3 mol C m−2 yr−1 east of 160°W to 0.5 ± 0.7 mol C m−2 yr−1 west of 170°E. Existing productivity rate estimates from time series stations are consistent with our regional productivity rate estimates in the eastern but not western North Pacific. These results highlight the need to estimate productivity rates over broad spatial areas and throughout the full annual cycle including during winter ventilation in order to accurately estimate the rate and efficiency of carbon sequestration via the ocean's biological pump.This work was funded by a NDSEG Fellowship from the Office of Naval Research, a NSF Graduate Research Fellowship, and an ARCS Foundation Fellowship to H.I.P. and by NSF Ocean Sciences (0628663 and 1259055 to P.D.Q.).2016-08-2

    Perspectives on Chemical Oceanography in the 21st century: Participants of the COME ABOARD Meeting examine aspects of the field in the context of 40 years of DISCO

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    The questions that chemical oceanographers prioritize over the coming decades, and the methods we use to address these questions, will define our field's contribution to 21st century science. In recognition of this, the U.S. National Science Foundation and National Oceanic and Atmospheric Administration galvanized a community effort (the Chemical Oceanography MEeting: A BOttom-up Approach to Research Directions, or COME ABOARD) to synthesize bottom-up perspectives on selected areas of research in Chemical Oceanography. Representing only a small subset of the community, COME ABOARD participants did not attempt to identify targeted research directions for the field. Instead, we focused on how best to foster diverse research in Chemical Oceanography, placing emphasis on the following themes: strengthening our core chemical skillset; expanding our tools through collaboration with chemists, engineers, and computer scientists; considering new roles for large programs; enhancing interface research through interdisciplinary collaboration; and expanding ocean literacy by engaging with the public. For each theme, COME ABOARD participants reflected on the present state of Chemical Oceanography, where the community hopes to go and why, and actionable pathways to get there. A unifying concept among the discussions was that dissimilar funding structures and metrics of success may be required to accommodate the various levels of readiness and stages of knowledge development found throughout our community. In addition to the science, participants of the concurrent Dissertations Symposium in Chemical Oceanography (DISCO) XXV, a meeting of recent and forthcoming Ph.D. graduates in Chemical Oceanography, provided perspectives on how our field could show leadership in addressing long-standing diversity and early-career challenges that are pervasive throughout science. Here we summarize the COME ABOARD Meeting discussions, providing a synthesis of reflections and perspectives on the field

    Nonuniform ocean acidification and attenuation of the ocean carbon sink

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    Author Posting. © American Geophysical Union, 2017. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 44 (2017): 8404–8413, doi:10.1002/2017GL074389.Surface ocean carbon chemistry is changing rapidly. Partial pressures of carbon dioxide gas (pCO2) are rising, pH levels are declining, and the ocean's buffer capacity is eroding. Regional differences in short-term pH trends primarily have been attributed to physical and biological processes; however, heterogeneous seawater carbonate chemistry may also be playing an important role. Here we use Surface Ocean CO2 Atlas Version 4 data to develop 12 month gridded climatologies of carbonate system variables and explore the coherent spatial patterns of ocean acidification and attenuation in the ocean carbon sink caused by rising atmospheric pCO2. High-latitude regions exhibit the highest pH and buffer capacity sensitivities to pCO2 increases, while the equatorial Pacific is uniquely insensitive due to a newly defined aqueous CO2 concentration effect. Importantly, dissimilar regional pH trends do not necessarily equate to dissimilar acidity ([H+]) trends, indicating that [H+] is a more useful metric of acidification.2018-02-1

    OOI Biogeochemical Sensor Data: Best Practices and User Guide. Version 1.0.0.

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    The OOI Biogeochemical Sensor Data Best Practices and User Guide is intended to provide current and prospective users of data generated by biogeochemical sensors deployed on the Ocean Observatories Initiative (OOI) arrays with the information and guidance needed for them to ensure that the data is science-ready. This guide is aimed at researchers with an interest or some experience in ocean biogeochemical processes. We expect that users of this guide will have some background in oceanography, however we do not assume any prior experience working with biogeochemical sensors or their data. While initially envisioned as a “cookbook” for end users seeking to work with OOI biogeochemical (BGC) sensor data, our Working Group and Beta Testers realized that the processing required to meet the specific needs of all end users across a wide range of potential scientific applications and combinations of OOI BGC data from different sensors and platforms couldn’t be synthesized into a single “recipe”. We therefore provide here the background information and principles needed for the end user to successfully identify and understand all the available “ingredients” (data), the types of “cooking” (end user processing) that are recommended to prepare them, and a few sample “recipes” (worked examples) to support end users in developing their own “recipes” consistent with the best practices presented here. This is not intended to be an exhaustive guide to each of these sensors, but rather a synthesis of the key information to support OOI BGC sensor data users in preparing science-ready data products. In instances when more in-depth information might be helpful, references and links have been provided both within each chapter and in the Appendix
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