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  • Articles  (45)
  • 2000-2004  (32)
  • 1985-1989  (13)
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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 429 (2004), S. 349-349 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] ...As a child, I dreamed of being a scientist, but when I left middle school this looked impossible. Because of illness during my final exams, my grades were too low to obtain a stipend to continue to university, and so I switched to a shorter course in civil engineering. I found it interesting ...
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 415 (2002), S. 23-23 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] ...For the past three centuries, the effects of humans on the global environment have escalated. Because of these anthropogenic emissions of carbon dioxide, global climate may depart significantly from natural behaviour for many millennia to come. It seems appropriate to assign the term ...
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 330 (1987), S. 108-109 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] LIFE on Earth is in a constant state of flux, with new species emerging and others becoming extinct as a result of changing environmental pressures. The average life span of a species is 1-10 million years (Myr). The process is not steady, however, the most celebrated jolt being the ...
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 324 (1986), S. 651-655 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. 1 Size distributions of H"l"(H2O)n cluster ions (upper abscissa and left ordinate) for an altitude of 17 km, an H2O-vapour volume mixing ratio of 3 x 106 and temperatures of 180,190, 200, 210 and 220 K (thermodynamical data of Lau et a/.17). Also shown is the fraction F of H+(H2O)n ions (lower ...
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  • 5
    ISSN: 1432-0894
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract A one-dimensional coupled climate and chemistry model has been developed to estimate past and possible future changes in atmospheric temperatures and chemical composition due to human activities. The model takes into account heat flux into the oceans and uses a new tropospheric temperature lapse rate formulation. As found in other studies, we estimate that the combined “greenhouse effect” of CH4, O3, CF2Cl2, CFCl3 and N2O in the future will be about as large as that of CO2. Our model calculates an increase in average global surface temperatures by about 0.6°C since the start of the industrial era and predicts for A.D. 2050 a twice as large additional rise. Substantial depletions of ozone in the upper stratosphere by between 25% and 55% are calculated, depending on scenario. Accompanying temperature changes are between 15°C and 25°C. Bromine compounds are found to be important, if no rigid international regulations on CFC emissions are effective. Our model may, however, concivably underestimate possible effects of CFCl3, CF2Cl2, C2F3Cl3 and other CFC and organic bromine emissions on lower stratospheric ozone, because it can not simulate the rapid breakdown of ozone which is now being observed worldwide. An uncertainty study regarding the photochemistry of stratospheric ozone, especially in the region below about 25 km, is included. We propose a reaction, involving excited molecular oxygen formation from ozone photolysis, as a possible solution to the problem of ozone concentrations calculated to be too low above 45 km. We also estimate that tropospheric ozone concentrations have grown strongly in the northern hemisphere since pre-industrial times and that further large increases may take place, especially if global emissions of NOx from fossil fuel and biomass burning were to continue to increase. Growing NOx emissions from aircraft may play an important role in ozone concentrations in the upper troposphere and low stratosphere.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 3 (1985), S. 1-1 
    ISSN: 1573-0662
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
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  • 7
    ISSN: 1573-0662
    Keywords: non-methane hydrocarbons ; ozone ; HO x ; CO ; NO x ; tropospheric chemistry ; global ; 3-d modeling ; upper troposphere
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The impact of natural and anthropogenicnon-methane hydrocarbons (NMHC) on troposphericchemistry is investigated with the global,three-dimensional chemistry-transport model MOGUNTIA.This meteorologically simplified model allows theinclusion of a rather detailed scheme to describeNMHC oxidation chemistry. Comparing model resultscalculated with and without NMHC oxidation chemistryindicates that NMHC oxidation adds 40–60% to surfacecarbon monoxide (CO) levels over the continents andslightly less over the oceans. Free tropospheric COlevels increase by 30–60%. The overall yield of COfrom the NMHC mixture considered is calculated to beabout 0.4 CO per C atom. Organic nitrate formationduring NMHC oxidation, and their transport anddecomposition affect the global distribution of NO x and thereby O3 production. The impact of theshort-lived NMHC extends over the entire tropospheredue to the formation of longer-lived intermediateslike CO, and various carbonyl and carboxyl compounds.NMHC oxidation almost doubles the net photochemicalproduction of O3 in the troposphere and leads to20–80% higher O3 concentration inNO x -rich boundarylayers, with highest increases over and downwind ofthe industrial and biomass burning regions. Anincrease by 20–30% is calculated for the remotemarine atmosphere. At higher altitudes, smaller, butstill significant increases, in O3 concentrationsbetween 10 and 60% are calculated, maximizing in thetropics. NO from lightning also enhances the netchemical production of O3 by about 30%, leading to asimilar increase in the global mean OH radicalconcentration. NMHC oxidation decreases the OH radicalconcentrations in the continental boundary layer withlarge NMHC emissions by up to 20–60%. In the marineboundary layer (MBL) OH levels can increase in someregions by 10–20% depending on season and NO x levels.However, in most of the MBL OH will decrease by10–20% due to the increase in CO levels by NMHCoxidation chemistry. The large decreases especiallyover the continents strongly reduce the markedcontrasts in OHconcentrations between land and oceanwhich are calculated when only the backgroundchemistry is considered. In the middle troposphere, OHconcentrations are reduced by about 15%, although dueto the growth in CO. The overall effect of thesechanges on the tropospheric lifetime of CH4 is a 15%increase from 6.5 to 7.4 years. Biogenic hydrocarbonsdominate the impact of NMHC on global troposphericchemistry. Convection of hydrocarbon oxidationproducts: hydrogen peroxides and carbonyl compounds,especially acetone, is the main source of HO x in theupper troposphere. Convective transport and additionof NO from lightning are important for the O3 budgetin the free troposphere.
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  • 8
    ISSN: 1573-0662
    Keywords: isoprene oxidation ; global atmospheric modeling ; condensed chemical mechanism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract A new condensed isoprene oxidation mechanism forglobal atmospheric modeling (MIM) was derived from ahighly detailed master chemical mechanism (MCM). In abox model intercomparison covering a wide range ofboundary layer conditions the MIM was compared withthe MCM and with five other condensed mechanisms, someof which have already been used in global modelingstudies of nonmethane hydrocarbon chemistry. Theresults of MCM and MIM were generally in goodagreement, but the other tested mechanisms exhibitedsubstantial differences relative to the MCM as well asrelative to each other. Different formation yields,reactivities and degradation pathways of organicnitrates formed in the course of isoprene oxidationwere identified as a major reason for the deviations.The relevance of the box model results for chemistrytransport models is discussed, and the need for avalidated reference mechanism and for an improvedrepresentation of isoprene chemistry in global modelsis pointed out.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 37 (2000), S. 81-112 
    ISSN: 1573-0662
    Keywords: precipitation scavenging ; Henry's Lawdependence ; global model study ; convection ; gasrejection on freezing ; trace gas vertical transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract With the global Chemistry-Transport model MATCHsensitivity simulations were performed to determinethe degree to which especially upward transport ofgases from the earth's surface is limited byconvective and large-scale precipitation scavenging.When only dissolution of species in the liquid phaseis taken into account, mixing ratio reductions in themiddle and upper troposphere by ≈10% arecalculated for gases with a Henry's Law constant H of103 mol/l/atm. The removal increases to ≈50% forH = 104 mol/l/atm, and to 90% for H =105 mol/l/atm. We also consider scavenging by theice phase, which is generally much less efficient thanby the aqueous phase. In fact, rejection of gases fromfreezing water droplets may be a source of trace gasat higher altitudes.H2O2 and the strong acids (H2SO4,HNO3, HCl, HBr, HI) have such large solubilitiesthat they become largely removed by precipitation.When significant concentrations of these gases andsulfate aerosol exist above the liquid water domain ofthe atmosphere, they have likely been produced thereor at higher altitudes, although some could have comefrom trace gas rejection from ice particles or fromevaporating hydrometeors. Several other gases areaffected by precipitation, but not strongly enough toprevent fractional transfer to the middle and uppertroposphere: e.g., HNO4, HNO2 at pH ≤5,CH2O, the organic acids at pH ≤6,CH3SOCH3, HOCl, HOBr, and HOI. NH3 islargely removed by liquid phase scavenging at pH ≤7 and SO2 atpH ≥7. At pH less thanabout 6, upward transport of SO2 should largelydepend on the efficiency of oxidation processes in thewater droplets by O3 and H2O2.Most gases have solubilities which are too low forsignificant precipitation scavenging and aqueous phaseoxidation to occur. This holds, e.g., for O3, CO,the hydrocarbons, NO, NO2, HCN, CH3CN,CH3SCH3, CH3O2H, CH3CHOandhigher aldehydes, CH3OH and higher alcohols,peroxyacetylnitrate (PAN), CH3COCH3 andother ketones (note that some of these are not listedin Table I because their solubilities are below 10mol/l/atm). Especially for the short-lived gases,transfer from the boundary layer to the middle andupper troposphere is actually promoted by the enhancedupward transport that occurs in clouds.
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  • 10
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