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  • AGU (American Geophysical Union)  (3)
  • 1
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    AGU (American Geophysical Union)
    In:  Eos, Transactions American Geophysical Union, 89 (43).
    Publication Date: 2017-03-03
    Type: Article , NonPeerReviewed
    Format: text
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  • 2
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    AGU (American Geophysical Union)
    In:  Journal of Geophysical Research: Oceans, 117 . C01021.
    Publication Date: 2018-02-27
    Description: In this study, results from the Baltic Sea Tracer Release Experiment (BATRE) are described, in which deep water mixing rates and mixing processes in the central Baltic Sea were investigated. In September 2007, an inert tracer gas (CF3SF5) was injected at approximately 200 m depth in the Gotland Basin, and the subsequent spreading of the tracer was observed during six surveys until February 2009. These data describe the diapycnal and lateral mixing during a stagnation period without any significant deep water renewal due to inflow events. As one of the main results, vertical mixing rates were found to dramatically increase after the tracer had reached the lateral boundaries of the basin, suggesting boundary mixing as the key process for basin-scale vertical mixing. Basin-scale vertical diffusivities were of the order of 10−5 m2 s−1 (about 1 order of magnitude larger than interior diffusivities) with evidence for a seasonal and vertical variability. In contrast to tracer experiments in the open ocean, the basin geometry (hypsography) was found to have a crucial impact on the vertical tracer spreading. The e-folding time scale for deep water renewal due to mixing was slightly less than 2 years, the time scale for the lateral homogenization of the tracer patch was of the order of a few months. Key Points: Mixing rates in the Gotland Basin are dominated by boundary mixing processes; The time scale for Gotland Basin deep water renewal is approximately 2 years; Mixing rates determined from the tracer CF3SF5
    Type: Article , PeerReviewed
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  • 3
    Publication Date: 2024-02-07
    Description: Upward transport and/or mixing of trace gas-enriched subsurface waters fosters the exchange of nitrous oxide (N2O) and methane (CH4) with the atmosphere in the Eastern-South Atlantic (ESA). To date, it is, however, unclear whether this source is maintained by local production or advection of trace gas-enriched water masses. The meridional and zonal variability of N2O and CH4 in the ESA were investigated to identify the contributions of the major regional water masses to the overall budget of N2O and CH4. The maximal sea surface N2O and CH4 concentrations and the main ESA upwelling cells co-occurred with a strong negative correlation with the sea surface temperature (SST) (p 〈 0.05). The dominance of the central water masses in the winter and spring seasons and the interplay between shelf topography and wind regime are suggested to determine enhanced gas transfer toward the sea-air interface or “capping” at midwater depth. These parameters are supposed to be critical in the local budget of N2O and CH4 in the ESA. Our findings also show that the shape of N2O and CH4 gradients is very similar both meridionally and zonally; however, the extent of the differences between the high-end and low-end members of the concentrations/saturations range is different. This suggests a more pronounced effect of local sources on CH4 than N2O distribution, in particular in the Walvis Bay area. With respect to N2O, however, low-oxygen waters from the poleward undercurrent impinge in the shelf close to Cape Frio and often result in N2O concentrations significantly higher than off Lüderitz (p 〈 0.05)
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
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