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  • 1
    In: Frontiers in Marine Science, Frontiers Media SA, Vol. 8 ( 2021-12-8)
    Type of Medium: Online Resource
    ISSN: 2296-7745
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2021
    detail.hit.zdb_id: 2757748-X
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  • 2
    In: Global Biogeochemical Cycles, American Geophysical Union (AGU), Vol. 27, No. 3 ( 2013-09), p. 950-961
    Abstract: At the surface, SAM-enhanced DIC is partly compensated by enhanced alkalinity The mixed‐layer DIC in the AZ increases mainly from vertical diffusion
    Type of Medium: Online Resource
    ISSN: 0886-6236 , 1944-9224
    URL: Issue
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2013
    detail.hit.zdb_id: 2021601-4
    SSG: 12
    SSG: 13
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  • 3
    In: Global Biogeochemical Cycles, American Geophysical Union (AGU), Vol. 37, No. 9 ( 2023-09)
    Abstract: p CO 2 seasonal cycle amplitude changes over 1985–2018 are detectable against both mapping uncertainty and natural variability uncertainty The dominant driver of p CO 2 amplitude increases over decadal timescales is attributed to the direct effect of C ant invasion A discrepancy is found with surface dissolved inorganic carbon (DIC) seasonality being systematically less in global ocean biogeochemistry models than in surface DIC observation‐based products
    Type of Medium: Online Resource
    ISSN: 0886-6236 , 1944-9224
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2023
    detail.hit.zdb_id: 2021601-4
    SSG: 12
    SSG: 13
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  • 4
    Online Resource
    Online Resource
    Copernicus GmbH ; 2021
    In:  Ocean Science Vol. 17, No. 4 ( 2021-08-02), p. 1011-1030
    In: Ocean Science, Copernicus GmbH, Vol. 17, No. 4 ( 2021-08-02), p. 1011-1030
    Abstract: Abstract. To derive an optimal observation system for surface ocean pCO2 in the Atlantic Ocean and the Atlantic sector of the Southern Ocean, 11 observation system simulation experiments (OSSEs) were completed. Each OSSE is a feedforward neural network (FFNN) that is based on a different data distribution and provides ocean surface pCO2 for the period 2008–2010 with a 5 d time interval. Based on the geographical and time positions from three observational platforms, volunteering observing ships, Argo floats and OceanSITES moorings, pseudo-observations were constructed using the outputs from an online-coupled physical–biogeochemical global ocean model with 0.25∘ nominal resolution. The aim of this work was to find an optimal spatial distribution of observations to supplement the widely used Surface Ocean CO2 Atlas (SOCAT) and to improve the accuracy of ocean surface pCO2 reconstructions. OSSEs showed that the additional data from mooring stations and an improved coverage of the Southern Hemisphere with biogeochemical ARGO floats corresponding to least 25 % of the density of active floats (2008–2010) (OSSE 10) would significantly improve the pCO2 reconstruction and reduce the bias of derived estimates of sea–air CO2 fluxes by 74 % compared to ocean model outputs.
    Type of Medium: Online Resource
    ISSN: 1812-0792
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2021
    detail.hit.zdb_id: 2183769-7
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  • 5
    Online Resource
    Online Resource
    Copernicus GmbH ; 2018
    In:  Biogeosciences Vol. 15, No. 14 ( 2018-07-30), p. 4661-4682
    In: Biogeosciences, Copernicus GmbH, Vol. 15, No. 14 ( 2018-07-30), p. 4661-4682
    Abstract: Abstract. The North Atlantic Ocean is a major sink region for atmospheric CO2 and contributes to the storage of anthropogenic carbon (Cant). While there is general agreement that the intensity of the meridional overturning circulation (MOC) modulates uptake, transport and storage of Cant in the North Atlantic Subpolar Ocean, processes controlling their recent variability and evolution over the 21st century remain uncertain. This study investigates the relationship between transport, air–sea flux and storage rate of Cant in the North Atlantic Subpolar Ocean over the past 53 years. Its relies on the combined analysis of a multiannual in situ data set and outputs from a global biogeochemical ocean general circulation model (NEMO–PISCES) at 1∕2∘ spatial resolution forced by an atmospheric reanalysis. Despite an underestimation of Cant transport and an overestimation of anthropogenic air–sea CO2 flux in the model, the interannual variability of the regional Cant storage rate and its driving processes were well simulated by the model. Analysis of the multi-decadal simulation revealed that the MOC intensity variability was the major driver of the Cant transport variability at 25 and 36∘ N, but not at OVIDE. At the subpolar OVIDE section, the interannual variability of Cant transport was controlled by the accumulation of Cant in the MOC upper limb. At multi-decadal timescales, long-term changes in the North Atlantic storage rate of Cant were driven by the increase in air–sea fluxes of anthropogenic CO2. North Atlantic Central Water played a key role for storing Cant in the upper layer of the subtropical region and for supplying Cant to Intermediate Water and North Atlantic Deep Water. The transfer of Cant from surface to deep waters occurred mainly north of the OVIDE section. Most of the Cant transferred to the deep ocean was stored in the subpolar region, while the remainder was exported to the subtropical gyre within the lower MOC.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2158181-2
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  • 6
    Online Resource
    Online Resource
    Copernicus GmbH ; 2019
    In:  Biogeosciences Vol. 16, No. 11 ( 2019-06-07), p. 2343-2367
    In: Biogeosciences, Copernicus GmbH, Vol. 16, No. 11 ( 2019-06-07), p. 2343-2367
    Abstract: Abstract. The Arctic Ocean is projected to experience not only amplified climate change but also amplified ocean acidification. Modeling future acidification depends on our ability to simulate baseline conditions and changes over the industrial era. Such centennial-scale changes require a global model to account for exchange between the Arctic and surrounding regions. Yet the coarse resolution of typical global models may poorly resolve that exchange as well as critical features of Arctic Ocean circulation. Here we assess how simulations of Arctic Ocean storage of anthropogenic carbon (Cant), the main driver of open-ocean acidification, differ when moving from coarse to eddy-admitting resolution in a global ocean-circulation–biogeochemistry model (Nucleus for European Modeling of the Ocean, NEMO; Pelagic Interactions Scheme for Carbon and Ecosystem Studies, PISCES). The Arctic's regional storage of Cant is enhanced as model resolution increases. While the coarse-resolution model configuration ORCA2 (2∘) stores 2.0 Pg C in the Arctic Ocean between 1765 and 2005, the eddy-admitting versions ORCA05 and ORCA025 (1∕2∘ and 1∕4∘) store 2.4 and 2.6 Pg C. The difference in inventory between model resolutions that is accounted for is only from their divergence after 1958, when ORCA2 and ORCA025 were initialized with output from the intermediate-resolution configuration (ORCA05). The difference would have been larger had all model resolutions been initialized in 1765 as was ORCA05. The ORCA025 Arctic Cant storage estimate of 2.6 Pg C should be considered a lower limit because that model generally underestimates observed CFC-12 concentrations. It reinforces the lower limit from a previous data-based approach (2.5 to 3.3 Pg C). Independent of model resolution, there was roughly 3 times as much Cant that entered the Arctic Ocean through lateral transport than via the flux of CO2 across the air–sea interface. Wider comparison to nine earth system models that participated in the Coupled Model Intercomparison Project Phase 5 (CMIP5) reveals much larger diversity of stored Cant and lateral transport. Only the CMIP5 models with higher lateral transport obtain Cant inventories that are close to the data-based estimates. Increasing resolution also enhances acidification, e.g., with greater shoaling of the Arctic's average depth of the aragonite saturation horizon during 1960–2012, from 50 m in ORCA2 to 210 m in ORCA025. Even higher model resolution would likely further improve such estimates, but its prohibitive costs also call for other more practical avenues for improvement, e.g., through model nesting, addition of coastal processes, and refinement of subgrid-scale parameterizations.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2019
    detail.hit.zdb_id: 2158181-2
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  • 7
    In: Biogeosciences, Copernicus GmbH, Vol. 19, No. 4 ( 2022-02-21), p. 1087-1109
    Abstract: Abstract. We have estimated global air–sea CO2 fluxes (fgCO2) from the open ocean to coastal seas. Fluxes and associated uncertainty are computed from an ensemble-based reconstruction of CO2 sea surface partial pressure (pCO2) maps trained with gridded data from the Surface Ocean CO2 Atlas v2020 database. The ensemble mean (which is the best estimate provided by the approach) fits independent data well, and a broad agreement between the spatial distribution of model–data differences and the ensemble standard deviation (which is our model uncertainty estimate) is seen. Ensemble-based uncertainty estimates are denoted by ±1σ. The space–time-varying uncertainty fields identify oceanic regions where improvements in data reconstruction and extensions of the observational network are needed. Poor reconstructions of pCO2 are primarily found over the coasts and/or in regions with sparse observations, while fgCO2 estimates with the largest uncertainty are observed over the open Southern Ocean (44∘ S southward), the subpolar regions, the Indian Ocean gyre, and upwelling systems. Our estimate of the global net sink for the period 1985–2019 is 1.643±0.125 PgC yr−1 including 0.150±0.010 PgC yr−1 for the coastal net sink. Among the ocean basins, the Subtropical Pacific (18–49∘ N) and the Subpolar Atlantic (49–76∘ N) appear to be the strongest CO2 sinks for the open ocean and the coastal ocean, respectively. Based on mean flux density per unit area, the most intense CO2 drawdown is, however, observed over the Arctic (76∘ N poleward) followed by the Subpolar Atlantic and Subtropical Pacific for both open-ocean and coastal sectors. Reconstruction results also show significant changes in the global annual integral of all open- and coastal-ocean CO2 fluxes with a growth rate of +0.062±0.006 PgC yr−2 and a temporal standard deviation of 0.526±0.022 PgC yr−1 over the 35-year period. The link between the large interannual to multi-year variations of the global net sink and the El Niño–Southern Oscillation climate variability is reconfirmed.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2022
    detail.hit.zdb_id: 2158181-2
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  • 8
    Online Resource
    Online Resource
    Copernicus GmbH ; 2016
    In:  Biogeosciences Vol. 13, No. 14 ( 2016-07-22), p. 4167-4185
    In: Biogeosciences, Copernicus GmbH, Vol. 13, No. 14 ( 2016-07-22), p. 4167-4185
    Abstract: Abstract. Anthropogenic changes in atmosphere–ocean and atmosphere–land CO2 fluxes have been quantified extensively, but few studies have addressed the connection between land and ocean. In this transition zone, the coastal ocean, spatial and temporal data coverage is inadequate to assess its global budget. Thus we use a global ocean biogeochemical model to assess the coastal ocean's global inventory of anthropogenic CO2 and its spatial variability. We used an intermediate resolution, eddying version of the NEMO-PISCES model (ORCA05), varying from 20 to 50 km horizontally, i.e. coarse enough to allow multiple century-scale simulations but finer than coarse-resolution models (∼  200 km) to better resolve coastal bathymetry and complex coastal currents. Here we define the coastal zone as the continental shelf area, excluding the proximal zone. Evaluation of the simulated air–sea fluxes of total CO2 for 45 coastal regions gave a correlation coefficient R of 0.8 when compared to observation-based estimates. Simulated global uptake of anthropogenic carbon results averaged 2.3 Pg C yr−1 during the years 1993–2012, consistent with previous estimates. Yet only 0.1 Pg C yr−1 of that is absorbed by the global coastal ocean. That represents 4.5 % of the anthropogenic carbon uptake of the global ocean, less than the 7.5 % proportion of coastal-to-global-ocean surface areas. Coastal uptake is weakened due to a bottleneck in offshore transport, which is inadequate to reduce the mean anthropogenic carbon concentration of coastal waters to the mean level found in the open-ocean mixed layer.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2016
    detail.hit.zdb_id: 2158181-2
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  • 9
    Online Resource
    Online Resource
    Copernicus GmbH ; 2018
    In:  Biogeosciences Vol. 15, No. 11 ( 2018-06-14), p. 3521-3539
    In: Biogeosciences, Copernicus GmbH, Vol. 15, No. 11 ( 2018-06-14), p. 3521-3539
    Abstract: Abstract. Concentrations of dissolved 230Th in the ocean water column increase with depth due to scavenging and downward particle flux. Due to the 230Th scavenging process, any change in the calcium carbonate (CaCO3) fraction of the marine particle flux due to changes in biological CaCO3 hard-shell production as a consequence of progressing ocean acidification would be reflected in the dissolved 230Th activity. Our prognostic simulations with a biogeochemical ocean general circulation model using different scenarios for the reduction of CaCO3 production under ocean acidification and different greenhouse gas emission scenarios – the Representative Concentration Pathways (RCPs) 8.5 to 2.6 – reveal the potential for deep 230Th measurements to detect reduced CaCO3 production at the sea surface. The time of emergence of an acidification-induced signal on dissolved 230Th is of the same order of magnitude as for alkalinity measurements. Interannual and decadal variability in factors other than a reduction in CaCO3 hard-shell production may mask the ocean-acidification-induced signal in dissolved 230Th and make detection of the pure CaCO3-induced signal more difficult so that only really strong changes in marine CaCO3 export would be unambiguously identifiable soon. Nevertheless, the impacts of changes in CaCO3 export production on marine 230Th are stronger than those for changes in POC (particulate organic carbon) or clay fluxes.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2158181-2
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  • 10
    In: Biogeosciences, Copernicus GmbH, Vol. 14, No. 5 ( 2017-03-09), p. 1123-1152
    Abstract: Abstract. Dissolved manganese (Mn) is a biologically essential element. Moreover, its oxidised form is involved in removing itself and several other trace elements from ocean waters. Here we report the longest thus far (17 500 km length) full-depth ocean section of dissolved Mn in the west Atlantic Ocean, comprising 1320 data values of high accuracy. This is the GA02 transect that is part of the GEOTRACES programme, which aims to understand trace element distributions. The goal of this study is to combine these new observations with new, state-of-the-art, modelling to give a first assessment of the main sources and redistribution of Mn throughout the ocean. To this end, we simulate the distribution of dissolved Mn using a global-scale circulation model. This first model includes simple parameterisations to account for the sources, processes and sinks of Mn in the ocean. Oxidation and (photo)reduction, aggregation and settling, as well as biological uptake and remineralisation by plankton are included in the model. Our model provides, together with the observations, the following insights: – The high surface concentrations of manganese are caused by the combination of photoreduction and sources contributing to the upper ocean. The most important sources are sediments, dust, and, more locally, rivers. – Observations and model simulations suggest that surface Mn in the Atlantic Ocean moves downwards into the southward-flowing North Atlantic Deep Water (NADW), but because of strong removal rates there is no elevated concentration of Mn visible any more in the NADW south of 40° N. – The model predicts lower dissolved Mn in surface waters of the Pacific Ocean than the observed concentrations. The intense oxygen minimum zone (OMZ) in subsurface waters is deemed to be a major source of dissolved Mn also mixing upwards into surface waters, but the OMZ is not well represented by the model. Improved high-resolution simulation of the OMZ may solve this problem. – There is a mainly homogeneous background concentration of dissolved Mn of about 0.10–0.15 nM throughout most of the deep ocean. The model reproduces this by means of a threshold on particulate manganese oxides of 25 pM, suggesting that a minimal concentration of particulate Mn is needed before aggregation and removal become efficient. – The observed distinct hydrothermal signals are produced by assuming both a strong source and a strong removal of Mn near hydrothermal vents.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2017
    detail.hit.zdb_id: 2158181-2
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