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H. E. Scheel H. Areskoug H. Geiss B. Gomiscek K. Granby L. Haszpra L. Klasinc D. Kley T. Laurila A. Lindskog M. Roemer R. Schmitt P. Simmonds S. Solberg G. Toupance 《Journal of Atmospheric Chemistry》1997,28(1-3):11-28
Surface ozone data from 25 Europeanlow-altitude sites and mountain sites located between79°N and 28°N were studied. The analysiscovered the time period March 1989–February 1993.Average summer and winter O3 concentrations inthe boundary layer over the continent gave rise togradients that were strongest in the north-west tosouth-east direction and west-east direction, respectively. WintertimeO3 ranged from 19 to 27 ppbover the continent, compared to about 32 ppb at thewestern border, while for summer the continentalO3 values ranged between 39 and 56 ppb and theoceanic mixing ratios were around 37 ppb. In the lowerfree troposphere average wintertime O3 mixingratios were around 38 ppb, with only an 8 ppbdifference between 28°N and 79°N. For summerthe average O3 levels decreased from about 55 ppbover Central Europe to 32 ppb at 79°N. Inaddition, O3 and Ox(= O3 + NO2)in polluted and clean air were compared. Theamplitudes of the seasonal ozone variations increasedin the north-west to south-east direction, while thetime of the annual maximum was shifted from spring (atthe northerly sites) to late summer (at sites inAustria and Hungary), which reflected the contributionof photochemical ozone production in the lower partsof the troposphere. 相似文献
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Ocean Dynamics - Lagrangian particle tracking, based on currents derived from hydrodynamic models, is an important tool in quantifying bio-physical transports in the ocean. Particle tracking in the... 相似文献
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Abstract. Diet and foraging behavior of Octopus dofleini in Prince William Sound and Port Graham, Alaska, were studied from collections of den litter, measurements of octopuses and estimates of live prey abundance. Based on 193 den collections from depths of - 31 to + 1.3 m, a diet of hard-bodied prey could be identified. The five most common litter species made up 80% of the litter remains, with nearly 30 species of various taxa malung up the rest. The proportions of major hard-bodied prey species in each litter pile significantly differed with depth of den, associated substrata, presence of cobble and geographical location but not with the presence of boulders or outcrop, the density of kelp or season of litter collection. Octopus weight was not significantly correlated with the size of prey remains although O. dofleini may take a wide range of prey sizes once it reaches 2.5 kg. O. dofleini was more likely to be found at sites with crabs, although no litter species was significantly preferred over its estimated abundance, and one species was significantly avoided. These results suggest that O. dofleini includes suitable bivalve and crab species in its diet in relation to live abundance, while at the same time exercising an element of selectivity, as some species were actively avoided. Comparison of litter remains from the northern-most range of O. dofleini with those published for British Columbia show that diet breadth was similar, but the identity of major hard-bodied prey species was very different for Alaskan octopuses. 相似文献
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M.P.W. Schneider T. Scheel P. van Hees K. Kalbitz 《Geochimica et cosmochimica acta》2010,74(5):1606-3154
Amorphous Al hydroxides (am-Al(OH)3) strongly sorb and by this means likely protect dissolved organic matter (OM) against microbial decay in soils. We carried out batch sorption experiments (pH 4.5; 40 mg organic C L−1) with OM extracted from organic horizons under a Norway spruce and a European beech forest. The stabilization of OM by sorption was analyzed by comparing the CO2 mineralized during the incubation of sorbed and non-sorbed OM. The mineralization of OM was evaluated based in terms of (i) the availability of the am-Al(OH)3, thus surface OM loadings, (ii) spectral properties of OM, and (iii) the presence of phosphate as a competitor for OM. This was done by varying the solid-to-solution ratio (SSR = 0.02-1.2 g L−1) during sorption. At low SSRs, hence limited am-Al(OH)3 availability, only small portions of dissolved OM were sorbed; for OM from Oa horizons, the mineralization of the sorbed fraction exceeded that of the original dissolved OM. The likely reason is competition with phosphate for sorption sites favouring the formation of weak mineral-organic bindings and the surface accumulation of N-rich, less aromatic and less complex OM. This small fraction controlled the mineralization of sorbed OM even at higher SSRs. At higher SSRs, i.e., with am-Al(OH)3 more available, competition of phosphate decreased and aromatic compounds were sorbed selectively, which resulted in pronounced resistance of sorbed OM against decay. The combined OC mineralization of sorbed and non-sorbed OM was 12-65% less than that of the original DOM. Sorbed OM contributed only little to the overall OC mineralization. Stabilization of OC increased in direct proportion to am-Al(OH)3 availability, despite constant aromatic C (∼30%). The strong stabilization at higher mineral availability is primarily governed by strong Al-OM bonds formed under less competitive conditions. Due to these strong bonds and the resulting strong stabilization, the surface loading, a proxy for the mineral’s occupation by OM, was not a factor in the mineralization of sorbed OM over a wide range of C sorption (0.2-1.1 mg C m−2). This study demonstrates that sorption to am-Al(OH)3 results in stabilization of OM. The mineral availability as well as the inorganic solution chemistry control sorptive interactions, thereby the properties of sorbed OM, and the stability of OM against microbial decay. 相似文献
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Hans J. Scheel 《Natural Hazards》2014,70(1):951-956
Tsunami impact on a coast can be reduced by applying a submerged vertical barrier to reflect tsunami before the catastrophic waves are built up near the coast. However, construction of such long walls by conventional submarine technology is difficult. In this paper, the construction of extended submarine walls at a depth of between 50 and 500 m below sea level by a relatively simple and efficient technology is described. The submarine walls can consist either of high-strength steel fences with anchors or two parallel steel fences with distance holders, lowered into the sea and fixed with rocks inserted from top. Alternatively, the barriers could be built from gabions (prefabricated steel net baskets filled with rocks) and lowered into the sea. The space between these tsunami barriers and the coast can be filled with solid material, thus allowing reclamation of new land, or this gap can be used for fish farming. These barriers can contribute to preservation of beaches and natural ecosystems at the coast. 相似文献
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Biodegradation of forest floor organic matter bound to minerals via different binding mechanisms 总被引：6，自引：0，他引：6
Robert Mikutta Christian Mikutta Thorsten Scheel Reinhold Jahn 《Geochimica et cosmochimica acta》2007,71(10):2569-2590
Mineral-associated organic matter (OM) represents a large reservoir of organic carbon (OC) in natural environments. The factors controlling the extent of the mineral-mediated OC stabilization, however, are poorly understood. The protection of OM against biodegradation upon sorption to mineral phases is assumed to result from the formation of strong bonds that limit desorption. To test this, we studied the biodegradation of OM bound to goethite (α-FeOOH), pyrophyllite, and vermiculite via specific mechanisms as estimated from OC uptake in different background electrolytes and operationally defined as ‘ligand exchange’, ‘Ca2+ bridging’, and ‘van der Waals forces’. Organic matter extracted from an Oa forest floor horizon under Norway spruce (Picea abies (L.) Karst) was reacted with minerals at dissolved OC concentrations of ∼5-130 mg/L at pH 4. Goethite retained up to 30.1 mg OC/g predominantly by ‘ligand exchange’; pyrophyllite sorbed maximally 12.5 mg OC/g, largely via ‘van der Waals forces’ and ‘Ca2+ bridging’, while sorption of OM to vermiculite was 7.3 mg OC/g, mainly due to the formation of ‘Ca2+ bridges’. Aromatic OM components were selectively sorbed by all minerals (goethite ? phyllosilicates). The sorption of OM was strongly hysteretic with the desorption into 0.01 M NaCl being larger for OM held by ‘Ca2+ bridges’ and ‘van der Waals forces’ than by ‘ligand exchange’. Incubation experiments under aerobic conditions (initial pH 4; 90 days) revealed that OM mainly bound to minerals by ‘ligand exchange’ was more resistant against mineralization than OM held by non-columbic interactions (‘van der Waals forces’). Calcium bridges enhanced the stability of sorbed OM, especially for vermiculite, but less than the binding via ‘ligand exchange’. Combined evidence suggests that the extent and rate of mineralization of mineral-associated OM are governed by desorption. The intrinsic stability of sorbed OM as related to the presence of resistant, lignin-derived aromatic components appears less decisive for the sorptive stabilization of OM than the involved binding mechanisms. In a given environment, the type of minerals present and the solution chemistry determine the operating binding mechanisms, thereby the extent of OM sorption and desorption, and thus ultimately the bioavailability of mineral-associated OM. 相似文献
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Since 1978, a measuring station has been operated at Cape Point (34°21 S, 18°29 E). In this article, results of measurements of CO, CFCl3, CCl4, O3, N2O and CH4 are presented as monthly means and analyzed with respect to long-term trends and seasonal variations. For CO and CH4, very similar seasonal variations have been observed, indicating strong interrelations between these two gases. For CO and O3, no significant changes of the mean annual concentrations can be established for the observation periods of 10 and 5 years, respectively. The measurements yield a growth rate of 9.1 pptv yr-1 for CFCl3 (1980–1987) and 0.6 ppbv yr-1 for N2O (1983–1987). The concentration increases of CH4 (10.3 ppbv yr-1 for 1983–1987) and of CCl4 (2.1 pptv yr-1 for 1980–1988) are analyzed for temporal changes during the last years.Presented at the Second Conference on Baseline Observations in Atmospheric Chemistry (SABOAC II) in Melbourne, Australia, November 1988. 相似文献
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