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  • Articles  (13)
  • Climate change  (8)
  • Carbon cycle  (6)
  • 04. Solid Earth::04.06. Seismology::04.06.03. Earthquake source and dynamics
  • American Geophysical Union  (13)
  • American Institute of Physics
  • American Institute of Physics (AIP)
  • 2020-2023  (13)
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  • Articles  (13)
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  • 1
    Publication Date: 2022-10-26
    Description: 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(1), (2022): e2021GB007113, https://doi.org/10.1029/2021GB007113.
    Description: Stordalen Mire is a peatland in the discontinuous permafrost zone in arctic Sweden that exhibits a habitat gradient from permafrost palsa, to Sphagnum bog underlain by permafrost, to Eriophorum-dominated fully thawed fen. We used three independent approaches to evaluate the annual, multi-decadal, and millennial apparent carbon accumulation rates (aCAR) across this gradient: seven years of direct semi-continuous measurement of CO2 and CH4 exchange, and 21 core profiles for 210Pb and 14C peat dating. Year-round chamber measurements indicated net carbon balance of −13 ± 8, −49 ± 15, and −91 ± 43 g C m−2 y−1 for the years 2012–2018 in palsa, bog, and fen, respectively. Methane emission offset 2%, 7%, and 17% of the CO2 uptake rate across this gradient. Recent aCAR indicates higher C accumulation rates in surface peats in the palsa and bog compared to current CO2 fluxes, but these assessments are more similar in the fen. aCAR increased from low millennial-scale levels (17–29 g C m−2 y−1) to moderate aCAR of the past century (72–81 g C m−2 y−1) to higher recent aCAR of 90–147 g C m−2 y−1. Recent permafrost collapse, greater inundation and vegetation response has made the landscape a stronger CO2 sink, but this CO2 sink is increasingly offset by rising CH4 emissions, dominated by modern carbon as determined by 14C. The higher CH4 emissions result in higher net CO2-equivalent emissions, indicating that radiative forcing of this mire and similar permafrost ecosystems will exert a warming influence on future climate.
    Description: We would like to acknowledge the following funding in support of this project: Swedish Research Council (Vetenskapsrådet, VR) grants (NT 2007-4547 and NT 2013-5562 to P. Crill), U.S. Department of Energy grants (DE-SC0004632 and DE-SC0010580 to V. Rich and S. Saleska), and U.S. National Science Foundation MacroSystems Biology grant (NSF EF #1241037, PI Varner). This work was supported by the U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research under the Genomic Science program. We also acknowledge funding from the National Science Foundation for the EMERGE Biology Integration Institute, NSF Award #2022070.
    Description: 2022-07-03
    Keywords: Peat ; Carbon cycling ; Permafrost ; Carbon-14 ; Lead-210 ; Climate change
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  • 2
    Publication Date: 2022-10-26
    Description: 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 Journal of Geophysical Research: Oceans 127(1), (2022): e2021JC017424, https://doi.org/10.1029/2021JC017424.
    Description: By compiling boreal summer (June to October) CO2 measurements from 1989 to 2019 on the Bering and eastern Chukchi Sea shelves, we find that the study areas act as a CO2 sink except when impacted by river runoff and wind-driven upwelling. The CO2 system in this area is seasonally dominated by the biological pump especially in the northern Bering Sea and near Hanna Shoal, while wind-driven upwelling of CO2-rich bottom water can cause episodic outgassing. Seasonal surface ΔfCO2 (oceanic fCO2 – air fCO2) is dominantly driven by temperature only during periods of weak CO2 outgassing in shallow nearshore areas. However, after comparing the mean summer ΔfCO2 during the periods of 1989–2013 and 2014–2019, we suggest that temperature does drive long-term, multi-decadal patterns in ΔfCO2. In the northern Chukchi Sea, rapid warming concurrent with reduced seasonal sea-ice persistence caused the regional summer CO2 sink to decrease. By contrast, increasing primary productivity caused the regional summer CO2 sink on the Bering Sea shelf to increase over time. While additional time series are needed to confirm the seasonal and annual trajectory of CO2 changes and ocean acidification in these dynamic and spatially complex ecosystems, this study provides a meaningful mechanistic analysis of recent changes in inorganic carbonate chemistry. As high-resolution time series of inorganic carbonate parameters lengthen and short-term variations are better constrained in the coming decades, we will have stronger confidence in assessing the mechanisms contributing to long-term changes in the source/sink status of regional sub-Arctic seas.
    Description: We gratefully acknowledge the support of the funding agencies that supported this analysis, including the New Sustained Observations for Arctic Research project and the DBO-NCIS project (NA14OAR4320158, NA19OAR4320074) from the NOAA Arctic Research Program.
    Description: 2022-06-17
    Keywords: Pacific Arctic region ; Sea-air CO2 flux ; Ocean acidification ; Climate change ; Sea-ice loss ; Surface ocean CO2 Atlas
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  • 3
    Publication Date: 2022-12-23
    Description: 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 Geophysical Research Letters 49(12), (2022): e2021GL097598, https://doi.org/10.1029/2021GL097598.
    Description: The ocean is inhomogeneous in hydrographic properties with diverse water masses. Yet, how this inhomogeneity has evolved in a rapidly changing climate has not been investigated. Using multiple observational and reanalysis datasets, we show that the spatial standard deviation (SSD) of the global ocean has increased by 1.4 ± 0.1% in temperature and 1.5 ± 0.1% in salinity since 1960. A newly defined thermohaline inhomogeneity index, a holistic measure of both temperature and salinity changes, has increased by 2.4 ± 0.1%. Climate model simulations suggest that the observed ocean inhomogeneity increase is dominated by anthropogenic forcing and projected to accelerate by 200%–300% during 2015–2100. Geographically, the rapid upper-ocean warming at mid-to-low latitudes dominates the temperature inhomogeneity increase, while the increasing salinity inhomogeneity is mainly due to the amplified salinity contrast between the subtropical and subpolar latitudes.
    Description: This work is supported by the Strategic Priority Research Program of Chinese Academy of Sciences (grant XDB42000000 and XDB40000000), the National Key R&D Program of China (2017YFA0603200), and the Shandong Provincial Natural Science Foundation (ZR2020JQ17), and the U.S. National Science Foundation Physical Oceanography Program (OCE- 2048336).
    Description: 2022-12-23
    Keywords: Global ocean ; Temperature ; Salinity ; Spatial inhomogeneity ; Climate change
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  • 4
    Publication Date: 2022-11-06
    Description: 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(5), (2022): e2022GB007388, https://doi.org/10.1029/2022gb007388.
    Description: 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.
    Description: This work was funded by NSF OCE-1220301 to W.B., NSF OCE-1220600 to J.F.A., and startup funding for A.V.S.
    Description: 2022-11-06
    Keywords: Calcium carbonate ; Dissolution ; Carbon cycle
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  • 5
    Publication Date: 2022-10-27
    Description: Author Posting. © American Geophysical Union, 2021. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Biogeosciences 126(1), (2021): e2019JG005621, https://doi.org/10.1029/2019JG005621.
    Description: Ongoing ocean warming can release methane (CH4) currently stored in ocean sediments as free gas and gas hydrates. Once dissolved in ocean waters, this CH4 can be oxidized to carbon dioxide (CO2). While it has been hypothesized that the CO2 produced from aerobic CH4 oxidation could enhance ocean acidification, a previous study conducted in Hudson Canyon shows that CH4 oxidation has a small short‐term influence on ocean pH and dissolved inorganic radiocarbon. Here we expand upon that investigation to assess the impact of widespread CH4 seepage on CO2 chemistry and possible accumulation of this carbon injection along 234 km of the U.S. Mid‐Atlantic Bight. Consistent with the estimates from Hudson Canyon, we demonstrate that a small fraction of ancient CH4‐derived carbon is being assimilated into the dissolved inorganic radiocarbon (mean fraction of 0.5 ± 0.4%). The areas with the highest fractions of ancient carbon coincide with elevated CH4 concentration and active gas seepage. This suggests that aerobic CH4 oxidation has a greater influence on the dissolved inorganic pool in areas where CH4 concentrations are locally elevated, instead of displaying a cumulative effect downcurrent from widespread groupings of CH4 seeps. A first‐order approximation of the input rate of ancient‐derived dissolved inorganic carbon (DIC) into the waters overlying the northern U.S. Mid‐Atlantic Bight further suggests that oxidation of ancient CH4‐derived carbon is not negligible on the global scale and could contribute to deepwater acidification over longer time scales.
    Description: This study was sponsored by U.S. Department of Energy (DE‐FE0028980, awarded to J. D. K; DE‐FE0026195 interagency agreement with C. D. R.). We thank the crew of the R/V Hugh R. Sharp for their support, G. Hatcher, J. Borden, and M. Martini of the USGS for assistance with the LADCP, and Zach Bunnell, Lillian Henderson, and Allison Laubach for additional support at sea.
    Description: 2021-06-23
    Keywords: Radiocarbon ; Methane ; DIC ; Ocean acidification ; Climate change ; U.S Mid-Atlantic Bight
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  • 6
    Publication Date: 2022-10-19
    Description: Author Posting. © American Geophysical Union, 2021. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography and Paleoclimatology 36(7), (2021): e2020PA004088, https://doi.org/10.1029/2020PA004088.
    Description: We reconstruct deep water-mass salinities and spatial distributions in the western North Atlantic during the Last Glacial Maximum (LGM, 19–26 ka), a period when atmospheric CO2 was significantly lower than it is today. A reversal in the LGM Atlantic meridional bottom water salinity gradient has been hypothesized for several LGM water-mass reconstructions. Such a reversal has the potential to influence climate, ocean circulation, and atmospheric CO2 by increasing the thermal energy and carbon storage capacity of the deep ocean. To test this hypothesis, we reconstructed LGM bottom water salinity based on sedimentary porewater chloride profiles in a north-south transect of piston cores collected from the deep western North Atlantic. LGM bottom water salinity in the deep western North Atlantic determined by the density-based method is 3.41–3.99 ± 0.15% higher than modern values at these sites. This increase is consistent with: (a) the 3.6% global average salinity change expected from eustatic sea level rise, (b) a northward expansion of southern sourced deep water, (c) shoaling of northern sourced deep water, and (d) a reversal of the Atlantic's north-south deep water salinity gradient during the LGM.
    Description: This work was supported by the US National Science Foundation (grant numbers 1433150 and 1537485).
    Description: 2021-10-24
    Keywords: Carbon cycle ; Climate change ; Deep water ; Glaciation ; Meridional overturning circulation ; Paleosalinity ; Porewater
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  • 7
    Publication Date: 2022-10-20
    Description: Author Posting. © American Geophysical Union, 2021. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Water Resources Research 57(7), (2021): e2020WR028727, https://doi.org/10.1029/2020WR028727.
    Description: Numerous wetlands in the prairies of Canada provide important ecosystem services, yet are threatened by climate and land-use changes. Understanding the impacts of climate change on prairie wetlands is critical to effective conservation planning. In this study, we construct a wetland model with surface water balance and ecoregions to project future distribution of wetlands. The climatic conditions downscaled from the Weather Research and Forecasting model were used to drive the Noah-MP land surface model to obtain surface water balance. The climate change perturbation is derived from an ensemble of general circulation models using the pseudo global warming method, under the RCP8.5 emission scenario by the end of 21st century. The results show that climate change impacts on wetland extent are spatiotemporally heterogenous. Future wetter climate in the western Prairies will favor increased wetland abundance in both spring and summer. In the eastern Prairies, particularly in the mixed grassland and mid-boreal upland, wetland areas will increase in spring but experience enhanced declines in summer due to strong evapotranspiration. When these effects of climate change are considered in light of historical drainage, they suggest a need for diverse conservation and restoration strategies. For the mixed grassland in the western Canadian Prairies, wetland restoration will be favorable, while the highly drained eastern Prairies will be challenged by the intensified hydrological cycle. The outcomes of this study will be useful to conservation agencies to ensure that current investments will continue to provide good conservation returns in the future.
    Description: Z. Zhang was funded by a Mitacs Accelerate Fellowship funded by Ducks Unlimited Canada's Institute for Wetland and Waterfowl Research. Z. Zhang, Z. Li, and Y. Li acknowledge the financial support from the Natural Sciences and Engineering Research Council of Canada (NSERC) Discovery Grant, and Global Water Futures Program, Canada First Research Excellence Fund. This project was supported by grants from Wildlife Habitat Canada, Bass Pro Shops Cabela’s Outdoor Fund, and the Alberta NAWMP Partnership.
    Description: 2021-12-21
    Keywords: Wetland ; Hydrology ; Climate change ; Prairie Pothole Region ; Waterfowl ; Conservation
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  • 8
    Publication Date: 2022-10-20
    Description: Author Posting. © American Geophysical Union, 2021. 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 48(11), (2021): e2021GL093178, https://doi.org/10.1029/2021GL093178.
    Description: The effects of heterogeneous reactions between river-borne particles and the carbonate system were studied in the plumes of the Mississippi and Brazos rivers. Measurements within these plumes revealed significant removal of dissolved inorganic carbon (DIC) and total alkalinity (TA). After accounting for all known DIC and TA sinks and sources, heterogeneous reactions (i.e., heterogeneous CaCO3 precipitation and cation exchange between adsorbed and dissolved ions) were found to be responsible for a significant fraction of DIC and TA removal, exceeding 10% and 90%, respectively, in the Mississippi and Brazos plume waters. This finding was corroborated by laboratory experiments, in which the seeding of seawater with the riverine particles induced the removal of the DIC and TA. The combined results demonstrate that heterogeneous reactions may represent an important controlling mechanism of the seawater carbonate system in particle-rich coastal areas and may significantly impact the coastal carbon cycle.
    Description: This research was funded by the National Science Foundation (NSF) and the Bi-National Science Foundation U.S-Israel award number OCE-BSF 1635388.
    Description: 2021-11-20
    Keywords: Calcium carbonate ; Carbon cycle ; Carbonate chemistry ; Heterogeneous reactions ; Mississippi ; River mouths
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  • 9
    Publication Date: 2022-10-26
    Description: © The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Hayes, C. T., Costa, K. M., Anderson, R. F., Calvo, E., Chase, Z., Demina, L. L., Dutay, J., German, C. R., Heimburger-Boavida, L., Jaccard, S. L., Jacobel, A., Kohfeld, K. E., Kravchishina, M. D., Lippold, J., Mekik, F., Missiaen, L., Pavia, F. J., Paytan, A., Pedrosa-Pamies, R., Petrova, M., V., Rahman, S., Robinson, L. F., Roy-Barman, M., Sanchez-Vidal, A., Shiller, A., Tagliabue, A., Tessin, A. C., van Hulten, M., & Zhang, J. Global ocean sediment composition and burial flux in the deep sea. Global Biogeochemical Cycles, 35(4), (2021): e2020GB006769, https://doi.org/10.1029/2020GB006769.
    Description: Quantitative knowledge about the burial of sedimentary components at the seafloor has wide-ranging implications in ocean science, from global climate to continental weathering. The use of 230Th-normalized fluxes reduces uncertainties that many prior studies faced by accounting for the effects of sediment redistribution by bottom currents and minimizing the impact of age model uncertainty. Here we employ a recently compiled global data set of 230Th-normalized fluxes with an updated database of seafloor surface sediment composition to derive atlases of the deep-sea burial flux of calcium carbonate, biogenic opal, total organic carbon (TOC), nonbiogenic material, iron, mercury, and excess barium (Baxs). The spatial patterns of major component burial are mainly consistent with prior work, but the new quantitative estimates allow evaluations of deep-sea budgets. Our integrated deep-sea burial fluxes are 136 Tg C/yr CaCO3, 153 Tg Si/yr opal, 20Tg C/yr TOC, 220 Mg Hg/yr, and 2.6 Tg Baxs/yr. This opal flux is roughly a factor of 2 increase over previous estimates, with important implications for the global Si cycle. Sedimentary Fe fluxes reflect a mixture of sources including lithogenic material, hydrothermal inputs and authigenic phases. The fluxes of some commonly used paleo-productivity proxies (TOC, biogenic opal, and Baxs) are not well-correlated geographically with satellite-based productivity estimates. Our new compilation of sedimentary fluxes provides detailed regional and global information, which will help refine the understanding of sediment preservation.
    Description: 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. The 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, and the authors would like to acknowledge all attendees of this meeting. The authors acknowledge the participants of the 68th cruise of RV Akademik Mstislav Keldysh for helping acquire samples. Christopher T. Hayes acknowledges support from US-NSF awards 1658445 and 1737023. Some data compilation on Arctic shelf seas was supported by the Russian Science Foundation, grant number 20-17-00157. This work was also supported through project CRESCENDO (grant no. 641816, European Commission). Zanna Chase acknowledges support from the Australian Research Council’s Discovery Projects funding scheme (project DP180102357). Christopher R. German acknowledges US-NSF awards 1235248 and 1234827. Some colorbars used in the figures were designed by Kristen Thyng et al. (2016) and Patrick Rafter.
    Keywords: Barium ; Carbon cycle ; Marine atlas ; Mercury ; Opal ; Sediment burial
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  • 10
    Publication Date: 2022-10-26
    Description: Author Posting. © American Geophysical Union, 2021. 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 48(10), (2021): e2021GL092904, https://doi.org/10.1029/2021GL092904.
    Description: We report marine dissolved organic carbon (DOC) concentrations, and DOC Δ14C and δ13C values in seawater collected from the Southern Ocean and eastern Pacific GOSHIP cruise P18 in 2016/2017. The aging of 14C in DOC in circumpolar deep water northward from 69°S to 20°N was similar to that measured in dissolved inorganic carbon in the same samples, indicating that the transport of deep waters northward is the primary control of 14C in DIC and DOC. Low DOC ∆14C and δ13C measurements between 1,200 and 3,400 m depth may be evidence of a source of DOC produced in nearby hydrothermal ridge systems (East Pacific Rise).
    Description: This work was supported by NSF (OCE-1458941 and OCE-1951073 to Ellen R. M. Druffel), Fred Kavli Foundation, Keck Carbon Cycle AMS Laboratory, NSF/NOAA funded GO-SHIP Program, Canada Research Chairs program (to Brett D. Walker) and American Chemical Society Petroleum Research Fund New Directions (55,430-ND2 to Ellen R. M. Druffel and Brett D. Walker).
    Description: 2021-11-24
    Keywords: 13C ; Carbon cycle ; Circumpolar deep water ; Dissolved inorganic carbon ; Dissolved organic carbon ; Radiocarbon
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  • 11
    Publication Date: 2022-10-26
    Description: © The Author(s), 2019. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Proshutinsky, A., Krishfield, R., Toole, J. M., Timmermans, M-L., Williams, W. J., Zimmermann, S., Yamamoto-Kawai, M., Armitage, T. W. K., Dukhovskoy, D., Golubeva, E., Manucharyan, G. E., Platov, G., Watanabe, E., Kikuchi, T., Nishino, S., Itoh, M., Kang, S-H., Cho, K-H., Tateyama, K., & Zhao, J. Analysis of the Beaufort Gyre freshwater content in 2003-2018. Journal of Geophysical Research-Oceans, 124(12), (2019): 9658-9689, doi:10.1029/2019JC015281.
    Description: Hydrographic data collected from research cruises, bottom‐anchored moorings, drifting Ice‐Tethered Profilers, and satellite altimetry in the Beaufort Gyre region of the Arctic Ocean document an increase of more than 6,400 km3 of liquid freshwater content from 2003 to 2018: a 40% growth relative to the climatology of the 1970s. This fresh water accumulation is shown to result from persistent anticyclonic atmospheric wind forcing (1997–2018) accompanied by sea ice melt, a wind‐forced redirection of Mackenzie River discharge from predominantly eastward to westward flow, and a contribution of low salinity waters of Pacific Ocean origin via Bering Strait. Despite significant uncertainties in the different observations, this study has demonstrated the synergistic value of having multiple diverse datasets to obtain a more comprehensive understanding of Beaufort Gyre freshwater content variability. For example, Beaufort Gyre Observational System (BGOS) surveys clearly show the interannual increase in freshwater content, but without satellite or Ice‐Tethered Profiler measurements, it is not possible to resolve the seasonal cycle of freshwater content, which in fact is larger than the year‐to‐year variability, or the more subtle interannual variations.
    Description: National Science Foundation. Grant Numbers: PLR‐1302884,OPP‐1719280, and OPP‐1845877, PLR‐1303644 and OPP‐1756100, OPP‐1756100, PLR‐1303644, OPP‐1845877, OPP‐1719280, PLR‐1302884 Key Program of National Natural Science Foundation of China. Grant Number: 41330960 Global Change Research Program of China. Grant Number: 2015CB953900 Ministry of Education, Korea Japan Aerospace Exploration Agency (JAXA) /Earth Observation Research Center (EORC) Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) Stanback Postdoctoral Fellowship Russian Foundation for Basic Research. Grant Number: 17‐05‐00382 Presidium of Russian Academy of Sciences HYCOM NOPP. Grant Number: N00014‐15‐1‐2594 DOE. Grant Number: DE‐SC0014378 National Aeronautics and Space Administration Tokyo University of Marine Science and Technology Department of Fisheries and Oceans Canada Woods Hole Oceanographic Institution
    Keywords: Beaufort Gyre ; Arctic Ocean ; Freshwater balance ; Circulation ; Modeling ; Climate change
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  • 12
    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 Geophysical Research Letters 46(16), (2019): 9851-9860, doi:10.1029/2019GL083726.
    Description: Coral reef calcification is expected to decline due to climate change stressors such as ocean acidification and warming. Projections of future coral reef health are based on our understanding of the environmental drivers that affect calcification and dissolution. One such driver that may impact coral reef health is heterotrophy of oceanic‐sourced particulate organic matter, but its link to calcification has not been directly investigated in the field. In this study, we estimated net ecosystem calcification and oceanic particulate organic carbon (POCoc) uptake across the Kāne'ohe Bay barrier reef in Hawai'i. We show that higher rates of POCoc uptake correspond to greater net ecosystem calcification rates, even under low aragonite saturation states (Ωar). Hence, reductions in offshore productivity may negatively impact coral reefs by decreasing the food supply required to sustain calcification. Alternatively, coral reefs that receive ample inputs of POCoc may maintain higher calcification rates, despite a global decline in Ωar.
    Description: Data needed for calculations are available in the supporting information. Additional data can be provided upon request directly from the corresponding author or accessed by links provided in the supporting information. The authors declare no competing financial interests. We thank Texas Sea Grant for providing partial funding for this project to A. Kealoha through the Grants‐In‐Aid of Graduate Research Program. We also thank the NOAA Nancy Foster Scholarship for PhD program funding to A. Kealoha and Texas A&M University for funds awarded to Shamberger that supported this work. This research was also supported by funding from National Science Foundation Grant OCE‐1538628 to Rappé. The Hawaii Institute of Marine Biology (particularly the Rappé Lab and Jason Jones), NOAA's Coral Reef Ecosystem Program, Connie Previti, Serena Smith, and Chris Maupin were instrumental in sample collection and data analysis.
    Description: 2020-02-22
    Keywords: Coral reefs ; Ocean acidification ; Climate change ; Heterotrophy
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  • 13
    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 Journal of Geophysical Research: Biogeosciences 124(8), (2019): 2582-2594, doi: 10.1029/2019JG005107.
    Description: To assess the influences of carbon sources and transport processes on the 14C age of organic matter (OM) in continental margin sediments, we examined a suite of samples collected along a river‐shelf‐deep ocean transect in the East China Sea (ECS). Ramped pyrolysis‐oxidiation was conducted on suspended particulate matter in the Yangtze River and on surface sediments from the ECS shelf and northern Okinawa Trough. 14C ages were determined on OM decomposition products within different temperature windows. These measurements suggest that extensive amounts of pre‐old (i.e., millennial age) organic carbon (OC) are subject to degradation within and beyond the Yangtze River Delta, and this process is accompanied by an exchange of terrestrial and marine OM. These results, combined with fatty acid concentration data, suggest that both the nature and extent of OM preservation/degradation as well as the modes of transport influence the 14C ages of sedimentary OM. Additionally, we find that the age of (thermally) refractory OC increases during across‐shelf transport and that the age offset between the lowest and highest temperature OC decomposition fractions also increases along the shelf‐to‐trough transect. Amplified interfraction spread or 14C heterogeneity is the greatest in the Okinawa Trough. Aged sedimentary OM across the transect may be a consequence of several reasons including fossil OC input, selective degradation of younger OC, hydrodynamic sorting processes, and aging during lateral transport. Consequently, each of them should be considered in assessing the 14C results of sedimentary OM and its implications for the carbon cycle and interpretation of sedimentary records.
    Description: This study was supported by Doc. Mobility Fellowship (P1EZP2_159064; R. B.) from the Swiss National Science Foundation (SNSF). This study was also supported by SNF “CAPS‐LOCK” project 200021_140850 (T. I. E.), by the National Natural Science Foundation of China (NSFC; grants 41520104009 and 41630966, M. Z.), and by the “111” project (B13030). We are grateful for support of the NOSAMS staff in the execution of this project. We also appreciate the assistance from Yushuang Zhang (Ocean University of China) at NOSAMS and members of the Laboratory for Ion Beam Physics at ETH Zurich for AMS measurements. We acknowledge Lei Xing, Haidong Zhang, Guodong Song, Meng Yu, Yonghao Jia, and Shanshan Duan (Ocean University of China) for sampling assistance on the cruises. Assistance at sea by the crews of R/V Dongfanghong II and R/V Hakuhu Maru is also acknowledged. Readers can access or find the data from figures and tables in the supporting information.
    Keywords: Radiocarbon ; Carbon cycle ; Sediments ; Organic carbon ; Hydrodynamic processes
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