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  • 1
    Digitale Medien
    Digitale Medien
    [s.l.] : Nature Publishing Group
    Nature 378 (1995), S. 50-54 
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] Limited measurements of alcohols and carbonyls have been reported from ground sites generally in rural/urban environments5 7. Recently, we have developed and tested a semi-automated airborne instrument that uses a Reduction Gas Detector (ROD) for the sensitive (10 parts per trillion (1012) by ...
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    [s.l.] : Nature Publishing Group
    Nature 333 (1988), S. 51-52 
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] The air samples were collected in evacuated stainless steel electropolished canisters. Dissolved gas in seawater samples were stripped in situ with ultra-grade helium by a technique described by Bonsang et al.3. The analysis was performed in the laboratory by gas chromatography with a flame ...
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Journal of atmospheric chemistry 6 (1988), S. 3-20 
    ISSN: 1573-0662
    Schlagwort(e): Nonmethane hydrocarbons ; sea-air exchanges
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Geologie und Paläontologie
    Notizen: Abstract C2-C6 Nonmethane hydrocarbon (NMHC) concentrations in the atmospheric boundary layer and in surface seawater were simultaneously measured during an oceanographic cruise in the intertropical Indian Ocean. NMHC were found to be mainly C2-C4 alkenes and C2-C3 alkanes. Their concentrations ranged from 1 to 30×10−9 l/l in the seawater and 0.1 to 15 ppbv in the atmosphere. Seawater appeared to be a source because the C2-C6 NMHC were supersaturated with respect to the atmosphere by 2 or 3 orders of magnitude. After a selection of the pure marine atmospheric samples, performed with the help of stable and radioactive continental tracers, we found an identical composition in NMHC of surface air and seawater. This observation enabled us to establish that the gas transfer between sea and air occurred according to nonsteady state processes, and that the fluxes cannot be deduced only from atmospheric measurements. An order of magnitude value of the oceanic source for the different NMHC is however derived from the comparison of their sea water concentrations to that of propane and an independent evluation of the marine source of this last compound.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Journal of atmospheric chemistry 11 (1990), S. 169-178 
    ISSN: 1573-0662
    Schlagwort(e): Nonmethane hydrocarbons ; tropospheric chemistry ; background pollution ; air-sea exchanges
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Geologie und Paläontologie
    Notizen: Abstract Between January 1984 and May 1987, C2 to C5 NMHC concentrations, and Radon-222 activities were measured at Amsterdam Island in the Indian Ocean. A large variability of about one order of magnitude was observed in the NMHC concentrations. Most of the samples were collected under marine influence. Using ethene as a reference compound for marine emissions, it appears that the NMHC/ethene composition of the air and its variability directly reflect the composition of dissolved gases in surface seawater. Only the ethane/ethene ratio presents a significant deviation from this typical composition and this can be attributed to a continental component. At sea level, the reation frequency of OH radicals with the NMHC is similar to that of methane and carbon monoxide. Thus, the contribution of marine NMHC should be taken into account in the modelling of oxidants in remote atmospheres.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Journal of atmospheric chemistry 25 (1996), S. 115-148 
    ISSN: 1573-0662
    Schlagwort(e): NMHC budget ; tropospheric distributions ; methane budget ; TROPOZ II experiment
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Geologie und Paläontologie
    Notizen: Abstract One hundred atmospheric samples were collected aboard the French Caravelle research aircraft, during the TROPOZ II experiment (January 1991). Tropospheric meridional distributions versus height were then derived from 70° N to 60° S and between 0.25 km and 11 km for methane, acetylene, ethane and propane. Areas of significant emissions were identified over northern latitudes with, for acetylene, maximum mixing ratios in the north (1.896 ppbv) more than 70 times higher than in background southern latitudes (0.025 ppbv). The influence of emissions from biomass burning was also obvious in the tropical boundary layer. Significant dynamic phenomena led to high mixing ratio zones above 8 or 10 km even for the most reactive hydrocarbons. For the first time, simultaneous assessment of global tropospheric contents of several light hydrocarbons was carried out. Using TROPOZ II data (January 1991) and STRATOZ III data (June 1984) collected by Rudolph (1988) during similar aircraft flights in 1988, the following tropospheric loads (in Tg-compound) were estimated, in January 1991 and June 1984, respectively: 1.1 and 0.4 for acetylene, 5.0 and 3.9 for ethane, 3.6 and 1.4 for propane and 3545 for methane in January only. According to our results, 40 to 65% of acetylene and alkanes are oxidized in the tropics. In addition, by computing the annual tropospheric sink of acetylene and alkanes, an evaluation of their annual global fluxes was performed. The figures are, in Tg-compound y-1 with an uncertainty of 80% to an order of magnitude, based on January and June data, respectively: 10 and 6.6 for acetylene, 16.3 and 17.6 for ethane and 52.3 and 26.5 for propane.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Publikationsdatum: 2009-06-01
    Print ISSN: 0021-9584
    Digitale ISSN: 1938-1328
    Thema: Chemie und Pharmazie , Pädagogik
    Publiziert von American Chemical Society
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Publikationsdatum: 2019
    Beschreibung: 〈p〉Atmospheric deposition is a source of potentially bioavailable iron (Fe) and thus can partially control biological productivity in large parts of the ocean. However, the explanation of observed high aerosol Fe solubility compared to that in soil particles is still controversial, as several hypotheses have been proposed to explain this observation. Here, a statistical analysis of aerosol Fe solubility estimated from four models and observations compiled from multiple field campaigns suggests that pyrogenic aerosols are the main sources of aerosols with high Fe solubility at low concentration. Additionally, we find that field data over the Southern Ocean display a much wider range in aerosol Fe solubility compared to the models, which indicate an underestimation of labile Fe concentrations by a factor of 15. These findings suggest that pyrogenic Fe-containing aerosols are important sources of atmospheric bioavailable Fe to the open ocean and crucial for predicting anthropogenic perturbations to marine productivity.〈/p〉
    Digitale ISSN: 2375-2548
    Thema: Allgemeine Naturwissenschaft
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Publikationsdatum: 2017-01-22
    Beschreibung: We report a new synthesis of best estimates of the inputs of fixed nitrogen to the world ocean via atmospheric deposition, and compare this to fluvial inputs and di-nitrogen fixation. We evaluate the scale of human perturbation of these fluxes. Fluvial inputs dominate inputs to the continental shelf, and we estimate about 75% of this fluvial nitrogen escapes from the shelf to the open ocean. Biological di-nitrogen fixation is the main external source of nitrogen to the open ocean, i.e. beyond the continental shelf. Atmospheric deposition is the primary mechanism by which land based nitrogen inputs, and hence human perturbations of the nitrogen cycle, reach the open ocean. We estimate that anthropogenic inputs are currently leading to an increase in overall ocean carbon sequestration of ~0.4% (equivalent to an uptake of 0.15 Pg C yr -1 and less than the Duce et al., 2008 estimate). The resulting reduction in climate change forcing from this ocean CO 2 uptake is offset to a small extent by an increase in ocean N 2 O emissions. We identify four important feedbacks in the ocean atmosphere nitrogen system that need to be better quantified to improve our understanding of the perturbation of ocean biogeochemistry by atmospheric nitrogen inputs. These feedbacks are recycling of (1) ammonia and (2) organic nitrogen from the ocean to the atmosphere and back, (3) the suppression of nitrogen fixation by increased nitrogen concentrations in surface waters from atmospheric deposition, and (4) increased loss of nitrogen from the ocean by denitrification due to increased productivity stimulated by atmospheric inputs.
    Print ISSN: 0886-6236
    Digitale ISSN: 1944-9224
    Thema: Biologie , Chemie und Pharmazie , Geographie , Geologie und Paläontologie , Physik
    Publiziert von Wiley im Namen von American Geophysical Union (AGU).
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Publikationsdatum: 2016-02-26
    Beschreibung: The historical and future impacts of atmospheric deposition of inorganic nitrogen (N) and phosphorus (P) on the marine ecosystem in the east Mediterranean Sea are investigated by using a 1D coupled physical– biogeochemical model, set up for the Cretan Sea as a representative area of the basin. For the present-day simulation (2010), the model is forced by observations of atmospheric deposition fluxes at Crete, while for the hindcast (1860) and forecast (2030) simulations, the changes in atmospheric deposition calculated by global chemistry–transport models are applied to the present-day observed fluxes. The impact of the atmospheric deposition on the fluxes of carbon in the food chain is calculated together with the contribution of human activities to these impacts. The results show that total phytoplanktonic biomass increased by 16% over the past 1.5 centuries. Small fractional changes in carbon fluxes and planktonic biomasses are predicted for the near future. Simulations show that atmospheric deposition of N and P may be the main mechanism responsible for the anomalous N:P ratio observed in the Mediterranean Sea.
    Print ISSN: 0022-4928
    Digitale ISSN: 1520-0469
    Thema: Geographie , Geologie und Paläontologie , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Publikationsdatum: 2016-04-25
    Beschreibung: Reactive nitrogen emissions into the atmosphere are increasing as a result of human activities, affecting nitrogen deposition to the surface and impacting the productivity of terrestrial and marine ecosystems. An atmospheric chemistry–transport model [Tracer Model 4 of the Environmental Chemical Processes Laboratory (TM4-ECPL)] is here used to calculate the global distribution of total nitrogen deposition, accounting for the first time for both its inorganic and organic fractions in gaseous and particulate phases and past and projected changes due to anthropogenic activities. The anthropogenic and biomass-burning Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) historical and RCP6.0 and RCP8.5 emissions scenarios are used. Accounting for organic nitrogen (ON) primary emissions, the present-day global nitrogen atmospheric source is about 60% anthropogenic, while total N deposition increases by about 20% relative to simulations without ON primary emissions. About 20%–25% of total deposited N is ON. About 10% of the emitted nitrogen oxides are deposited as ON instead of inorganic nitrogen (IN), as is considered in most global models. Almost a threefold increase over land (twofold over the ocean) has been calculated for soluble N deposition due to human activities from 1850 to present. The investigated projections indicate significant changes in the regional distribution of N deposition and chemical composition, with reduced compounds gaining importance relative to oxidized ones, but very small changes in the global total flux. Sensitivity simulations quantify uncertainties due to the investigated model parameterizations of IN partitioning onto aerosols and of N chemically fixed on organics to be within 10% for the total soluble N deposition and between 25% and 35% for the dissolved ON deposition. Larger uncertainties are associated with N emissions.
    Print ISSN: 0022-4928
    Digitale ISSN: 1520-0469
    Thema: Geographie , Geologie und Paläontologie , Physik
    Standort Signatur Erwartet Verfügbarkeit
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