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  • PANGAEA  (35)
  • AGU (American Geophysical Union)  (10)
  • Copernicus
  • ELSEVIER SCIENCE BV
  • 2020-2024  (28)
  • 2000-2004  (13)
  • 1995-1999  (3)
  • 1990-1994  (1)
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  • 1
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    AGU (American Geophysical Union)
    In:  Geophysical Research Letters, 24 . pp. 1763-1766.
    Publication Date: 2018-02-13
    Description: The partial pressure of CO2 (pCO2) was measured during the 1995 South-West Monsoon in the Arabian Sea. The Arabian Sea was characterized throughout by a moderate supersaturation of 12–30 µatm. The stable atmospheric pCO2 level was around 345 µatm. An extreme supersaturation was found in areas of coastal upwelling off the Omani coast with pCO2 peak values in surface waters of 750 µatm. Such two-fold saturation (218%) is rarely found elsewhere in open ocean environments. We also encountered cold upwelled water 300 nm off the Omani coast in the region of Ekman pumping, which was also characterized by a strongly elevated seawater pCO2 of up to 525 µatm. Due to the strong monsoonal wind forcing the Arabian Sea as a whole and the areas of upwelling in particular represent a significant source of atmospheric CO2 with flux densities from around 2 mmol m−2 d−1 in the open ocean to 119 mmol m−2 d−1 in coastal upwelling. Local air masses passing the area of coastal upwelling showed increasing CO2 concentrations, which are consistent with such strong emissions.
    Type: Article , PeerReviewed
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  • 2
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    AGU (American Geophysical Union)
    In:  Journal of Geophysical Research: Oceans, 99 (C2). pp. 3407-3415.
    Publication Date: 2018-04-27
    Description: The effect of dissolution from particulates into the supernatant solution in sediment trap sample cups has been measured for fatty acids. A mooring array with time series sediment traps was deployed in the northeast Atlantic Ocean (59°N, 21°W) for 14 months. Selected representative samples from the trap at 2200 m (poisoned with NaN3) were analyzed for total and free fatty acids in both the solution and particulate phase by means of gas chromatography‐mass spectrometry with an ion trap detector. The flux contribution of the dissolved total fatty acids (∑ DTFA) was found to be between 15 and 75% of the total flux (∑ TTFA, sum of the fluxes of total fatty acids in both particles and supernatants). Dissolved free fatty acids (∑ DFFA) represented 25–88% of the total flux of free fatty acids (∑ TFFA). Absolute concentrations of total and free fatty acids in both compartments are discussed in terms of the processes controlling the distribution between the two phases, for example, readsorption. Sample handling, poisoning, bacterial activity, and swimmers may also affect fatty acid distribution. Flux data (sum of particulate and dissolved fluxes) are presented for individual fatty acids. Also, the degree of dissolution of individual fatty acids is shown for one sample (dissolved fraction ranging between 16 and 98% of total flux).
    Type: Article , PeerReviewed
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  • 3
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    AGU (American Geophysical Union)
    In:  Global Biogeochemical Cycles, 17 (1). pp. 1005-1024.
    Publication Date: 2018-03-16
    Description: Temporal trends in oceanic dissolved inorganic carbon (DIC) and δ13C-DIC were reconstructed along five isopycnals in the upper 1000 m of the North Atlantic Ocean using a back-calculation approach. The mean anthropogenic DIC increase was 1.21 ± 0.07 μmol kg−1 yr−1 and the mean 13C decrease was −0.026 ± 0.002‰ yr−1, both in good agreement with the results from previous studies. The observed δ13C-DIC perturbation ratio is −0.024 ± 0.003‰ (μmol kg−1)−1. Our results indicate that the North Atlantic is able to maintain equilibrium with the anthropogenic perturbation for DIC and follows it with decadal time lag for δ13C. A CFC-calibrated one-dimensional isopycnal advection-diffusion model is used to evaluate temporal DIC and δ13C trends and perturbation ratios of the reconstructions. We investigate the time history of the air-sea CO2 and 13C disequilibria in the North Atlantic and discuss the importance of physical and biological processes in maintaining them. We find evidence that the North Atlantic Ocean is characterized by enhanced uptake of anthropogenic CO2. Also, we use the model to examine how the time rate of change of δ13C depends on changes in the temporal evolution of δ13C in the atmosphere. The model evolution explains the curious result that the time rate of change of surface water δ13C in the North Atlantic Ocean can exceed that observed concurrently in the atmosphere. Finally we introduce a powerful way of estimating the global air-sea pCO2 disequilibrium based on the oceanic δ13C-DIC perturbation ratio.
    Type: Article , PeerReviewed
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  • 4
    Publication Date: 2018-03-16
    Description: The results of 1 year of automated pCO2 measurements in 2002/2003 onboard the car carrier M/V Falstaff are presented and analyzed with regard to the driving forces that change the seawater pCO2 in the midlatitude North Atlantic Ocean. The pCO2 in surface seawater is controlled by thermodynamics, biology, air-sea gas exchange, and physical mixing. Here we estimate the effects on the annual cycle of pCO2 and relate this property to parameters like SST, nitrate, and chlorophyll. On the basis of the amplitude in seawater pCO2 for all 4° × 5° grid boxes, this region can be separated into an eastern and western basin. The annual pCO2 cycle in the eastern basin (10°W–35°W) is less variable, which can be related to the two counteracting effects of temperature and biology; air-sea gas exchange plays a minor role when using climatological MLD. In the western basin (36°W–70°W) the pCO2 amplitude is more variable and strongly follows the thermodynamic forcing, since the biological forcing (as derived from nitrate concentrations) is decreased. Biology and air-sea exchange strongly depend on the MLD and therefore also include physical mixing effects. The pCO2 data of the analyzed region between 34°N and 52°N compare well to the Takahashi et al. [2002] climatology except for regions north of 45°N during the wintertime where the bias is significant.
    Type: Article , PeerReviewed
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  • 5
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    AGU (American Geophysical Union)
    In:  Journal of Geophysical Research: Oceans, 103 (C9). pp. 18681-18689.
    Publication Date: 2018-04-30
    Description: The penetration of anthropogenic or “excess” CO2 into the North Atlantic Ocean was studied along WOCE‐WHP section A2 from 49°N/11°W to 43°N/49°W using hydrographic data obtained during the METEOR cruise 30–2 in October/November 1994. A backcalculation technique based on measurements of temperature, salinity, oxygen, alkalinity, and total dissolved inorganic carbon was applied to identify the excess CO2. Everywhere along the transect surface water contained almost its full component of anthropogenic CO2 ( ∼62 μmol kg−1). Furthermore, anthropogenic CO2 has penetrated through the entire water column in the western basin of the North Atlantic Ocean. Even in the deepest waters (5000 m) of the western basin a mean value of 10.4 μmol kg−1 excess CO2 was calculated. The maximum penetration depth of excess CO2 in the eastern basin of the North Atlantic Ocean was ∼3500 m with values falling below 5 μmol kg−1 in greater depths. These results compare well with distributions of carbontetrachloride. They are also in agreement with the current understanding of the role of the “global ocean conveyor belt” for the uptake of anthropogenic CO2 into the deep ocean.
    Type: Article , PeerReviewed
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  • 6
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    AGU (American Geophysical Union)
    In:  Geophysical Research Letters, 26 . pp. 2065-2068.
    Publication Date: 2018-02-13
    Description: We compare estimates of the anthropogenic CO2 content of seawater samples from the subpolar North Atlantic Ocean calculated on the basis of a back-calculation technique with measurements of the chlorofluorocarbon CFC-11. Estimated anthropogenic CO2 concentrations are in the range 10–80 µmol kg-1, while CFC-11 concentrations cover the full range from below detection limit to 〉 5 pmol kg-1 in waters at atmospheric equilibrium. The majority of the data points show a linear correlation between anthropogenic CO2 concentrations and CFC-11 saturation, which can only be explained by the strongly advective nature of the North Atlantic Ocean. Only deep eastern basin samples deviate from this general observation in that they show still significant concentrations of anthropogenic CO2 where CFC-11 is no longer detectable. In order to remove the influence of the Revelle factor reflected in the anthropogenic CO2 concentrations we have calculated 'excess' pCO2, showing an even tighter linear correlation with atmospheric equilibrium concentrations of CFC-11.
    Type: Article , PeerReviewed
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  • 7
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    AGU (American Geophysical Union)
    In:  Eos, Transactions American Geophysical Union, 84 (21). pp. 197-204.
    Publication Date: 2017-02-14
    Description: Recent measurements and model studies have consistently identified a decreasing trend in the concentration of dissolved O2 in the ocean over the last several decades. This trend has important implications for our understanding of anthropogenic climate change. First, the observed oceanic oxygen changes may be a signal of the beginning of a reorganization of large-scale ocean circulation in response to anthropogenic radiative forcing. Second, the repartitioning of oxygen between the ocean and the atmosphere requires a revision of the current atmospheric carbon budget and the estimates of the terrestrial and oceanic carbon sinks as calculated by the Intergovernmental Panel on Climate Change (IPCC) from measurements of atmospheric O2/N2.
    Type: Article , NonPeerReviewed
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  • 8
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    AGU (American Geophysical Union)
    In:  Geophysical Research Letters, 30 . pp. 1085-1088.
    Publication Date: 2018-02-20
    Description: Normalization to a constant salinity (S) is widely used for the adjustment of marine inorganic carbon chemistry data such as total alkalinity (AT) and total dissolved inorganic carbon (CT). This procedure traces back to the earliest studies in marine chemistry, but ignores the influence of riverine input of alkalinity and of dissolution of biogenic carbonates in the ocean. We tested different adjustment possibilities for AT and conclude that in most parts of the surface ocean the normalization concept does not reflect relationships which represent reality. In this paper, we propose a salinity adjustment based on a constant and region-specific term for S = 0, which expresses river run off, upwelling from below the lysocline, calcification, and lateral sea surface water exchange. One application of the normalization concept is its extension to AT and also CT predictions and implementation in models. We give a brief discussion on the usage of such extensions.
    Type: Article , PeerReviewed
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  • 9
    Publication Date: 2023-09-19
    Description: During Meteor cruise 55 a strong undersaturation of surface seawater with respect to atmospheric CO2 was found in the Amazon River plume which is advected into the surface circulation of the tropical Atlantic. A conservative estimate of the plume-related CO2 sink in the tropical Atlantic yields a net air-sea flux of 0.014 ± 0.005 Pg C yr−1. The corresponding average CO2 flux density of 1.35 mmol m−2 d−1 is of similar magnitude but opposite sign as found elsewhere in the slightly supersaturated tropical Atlantic illustrating the significant impact of the Amazon on the biogeochemistry of large ocean areas. The dramatic change of the CO2 saturation state from highly supersaturated river waters to markedly undersaturated surface waters in the plume can be explained by a combination of the effects of CO2 outgassing from river water, of mixing between river and ocean water on the CO2 system properties, and of strong biological carbon drawdown in the plume.
    Type: Article , PeerReviewed
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  • 10
    Publication Date: 2024-02-07
    Description: When organic matter from thawed permafrost is released, the sources and sinks of greenhouse gases (GHGs), like carbon dioxide (CO2) and methane (CH4) in Arctic rivers will be influenced in the future. However, the temporal variation, environmental controls, and magnitude of the Arctic riverine GHGs are largely unknown. We measured in situ high temporal resolution concentrations of CO2, CH4, and oxygen (O2) in the Ambolikha River in northeast Siberia between late June and early August 2019. During this period, the largely supersaturated riverine CO2 and CH4 concentrations decreased steadily by 90% and 78%, respectively, while the O2 concentrations increased by 22% and were driven by the decreasing water temperature. Estimated gas fluxes indicate that during late June 2019, significant emissions of CO2 and CH4 were sustained, possibly by external terrestrial sources during flooding, or due to lateral exchange with gas-rich downstream-flowing water. In July and early August, the river reversed its flow constantly and limited the water exchange at the site. The composition of dissolved organic matter and microbial communities analyzed in discrete samples also revealed a temporal shift. Furthermore, the cumulative total riverine CO2 emissions (36.8 gC-CO2 m−2) were nearly five times lower than the CO2 uptake at the adjacent floodplain. Emissions of riverine CH4 (0.21 gC-CH4 m−2) were 16 times lower than the floodplain CH4 emissions. Our study revealed that the hydraulic connectivity with the land in the late freshet, and reversing flow directions in Arctic streams in summer, regulate riverine carbon replenishment and emissions.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
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