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1.
We present the first application of a multi-stage impactor to study volcanic particle emissions to the troposphere from Masaya volcano, Nicaragua. Concentrations of soluble SO4 2–,Cl–, F–, NO3 –, K+, Na+,NH4 +, Ca2+ and Mg2+ were determined in 11 size bins from 0.07 m to >25.5 m. The near-source size distributions showed major modes at 0.5m (SO4 2–, H+,NH4 +); 0.2 m and 5.0 m (Cl–) and 2.0–5.0 m(F–). K+ and Na+ mirrored the SO4 2– size-resolvedconcentrations closely, suggesting that these were transported primarily asK2SO4 and Na2SO4 in acidic solution, while Mg2+ andCa2+ presented modes in both <1 m and >1 m particles. Changes in relative humidity were studied by comparing daytime (transparent plume) and night-time (condensed plume) results. Enhanced particle growth rates were observed in the night-time plume as well as preferential scavenging of soluble gases, such as HCl, by condensed water. Neutralisation of the acidic aerosol by background ammonia was observed at the crater rim and to a greater extent approximately 15 km downwind of the active crater. We report measurements of re-suspended near-source volcanic dust, which may form a component of the plume downwind. Elevated levels ofSO4 2–, Cl–, F–,H+, Na+, K+ and Mg2+ were observed around the 10 m particle diameter in this dust. The volcanic SO4 2– flux leaving the craterwas 0.07 kg s–1.  相似文献   

2.
An investigation of the influence of mineral dust ontrace gas cycles in the troposphere is carried out inthis study. A 3D regional scale atmospheric chemistrymodel (STEM-III) which includes aerosol processes isused for the numerical simulations for May 1987.Heterogeneous interactions between gaseous species(SO2, N2O5, HNO3, HO2andH2O2) and the dust particles are considered.Emissions of dust behind convective cold fronts aremodeled. The transport and distribution of mineraldust predicted from the model is compared withsatellite measurements (aerosol index from TOMS). Themodel is shown to capture the synoptic variability inthe observed aerosol index. Calculations show twomajor dust events in May 1987, during which thedust levels close to the source reach more than500 g/m3. The transport of dust is mostlyrestricted towards the north, with the net continentaloutflow of 6 Tg for the entire month. Results showthat the presence of mineral aerosol can greatlyimpact sulfate and nitrate distributions. Averagedover the month of May, the presence of dust isestimated to increase particulate sulfate and nitratelevels in east Asia by 40%. Furthermore, the sulfateand nitrate on the dust particles are predicted to beassociated with the coarse mode (3–5 m particlediameter), consistent with observations over Japan.The influence of mineral dust on the photochemicaloxidant cycle is also investigated. For the entiremonth, a5–10% decrease in boundary layer ozone ispredicted by the model closer to regions of higherdust levels. The ratio of nitric acid to NOx overmarine regions is reduced by a factor between 1 and 2in the boundary layer to more than 2 in the freetroposphere as a result of aerosol processes.  相似文献   

3.
During April 1986, as part of an international arctic air chemistry study (AGASP-2), ground level observations of aerosol trace elements, oxides of sulphur and nitrogen and particle number size distribution were made at Alert Canada (82.5N, 62.3W). Pollution haze was evident as indicated by daily aerosol number (size > 0.15 m diameter) and SO4 = concentrations in the range 125 – 260 cm–3 and 1.6 – 4.5 g m–3, respectively. Haze and associated acidic gases tended to increase throughout the period. SO2 and peroxyacetylnitrate (PAN) mixing ratios were in the range 140 – 480 and 370 – 590 ppt(v), respectively. About 88% of the total end-product nitrogen was in the form of PAN. In air dried to 2% relative humidity by warming to room temperature, the aerosol mass size distribution had a major mode at 0.3 m diameter and a minor one at 2.5 m. Aerosol mass below 1.5 m was well correlated with SO4 =, K+ and PAN. There was a steady increase in the oxidized fraction of total airborne sulphur and nitrogen oxide throughout April as the sun rose above the horizon and remained above. The mean oxidation rate of SO2 between Eurasia and Alert was estimated as 0.25 – 0.5% h–1. The molar ratio of total nitrogen oxide to total sulphur oxide in the arctic atmosphere (0.67±0.17) was comparable to that in European emissions. A remarkably strong inverse correlation of filterable Br and O3 led to the conclusion that O3 destruction and filterable Br production below the Arctic surface radiation inversion is associated with tropospheric photochemical reactions involving naturally occurring gaseous bromine compounds.  相似文献   

4.
Aerosol chemical composition and trace gas measurements were made at twolocations on the northeastern peninsula of Tenerife during the ACE-2HILLCLOUD experiment, between 28 June and 23 July 1997. Measurementswere made of coarse (#gt;2.5 m aerodynamic diameter) and fine (#lt; 2.5m) aerosol Cl–, NO3 –,SO4 2–, non-sea saltSO4 2– (NSSS),CH3SO3 – (MSA) andNH4 +, and gas phase dimethylsulphide (DMS), HCl,HNO3, SO2, CH3COOH, HCOOH andNH3. Size distributions were measured using a cascadeimpactor. Results show that in marine air masses NSSS and MSA wereformed via DMS oxidation, with additional NSSS present in air massescontaining a continental component. Using a Eulerian box model approachfor aerosols transported between upwind and downwind sites, a mean NSSSproduction rate of 4.36 × 10–4 gm–3 s–1 was calculated for daytimeclear sky periods (highest insolation), with values for cloudy periodsduring daytime and nighttime of 3.55 × 10–4 and2.40 × 10–4 g m–3s–1, respectively. The corresponding rates for MSA were6.23 × 10–6, 8.49 × 10–6and 6.95 × 10–6 g m–3s–1, respectively. Molar concentration ratios forMSA/NSSS were 8.7% (1.8–18.2%) and 1.9%(1.3–3.5%) in clean and polluted air masses, respectively.Reactions occurring within clouds appeared to have a greater influenceon rates of MSA production, than of NSSS, while conversely daytime gasphase reactions were more important for NSSS. For MSA, nighttimein-cloud oxidation rates exceeded rates of daytime gas phase productionvia OH oxidation of DMS. NSSS, MSA and ammonium had trimodal sizedistributions, with modes at 0.3, 4.0 and >10.0 m (NSSS andNH4 +), and 0.3, 1.5 and 4.0 m (MSA). Nosignificant production of other aerosol species was observed, with theexception of ammonium, which was formed at variable rates dependent onneutralisation of the aerosol with ammonia released from spatiallynon-uniform surface sources. Seasalt components were mainly present incoarse particles, although sub-micrometre chloride was also measured.Losses by deposition exceeded calculated expectations for all species,and were highest for the seasalt fraction and nitrate.  相似文献   

5.
Thermal and optical techniques were used at Barrow, Alaska during AGASP II (3/20/86–4/7/86) to measure in-situ variability of major aerosol components present in Arctic Haze. The experiment provided continuous data on the concentration, size distribution and relative proportions of sulfate species and refractory aerosol for particle diameters of 0.15 to 5 m. Filter samples were also taken for determination of aerosol optical absorption due to soot (EC-elemental carbon). Although pronounced haze events were absence during this period the haze aerosol present varied in concentration between 2 and 6 g/m3 but showed little change in relative constituents. Apart from local influences, the optical data indicated a persistent fine-mode sulfate aerosol with a NH4 +/SO4 – molar ratio of about 0.4 and a refractory component of somewhat less than 10% by mass. A preliminary comparison of soot estimates determined from the light absorption data with the size distributions of refractory aerosol observed independently by the optical particle counter showed good agreement during the sample period. In the absence of local pollution, values of single scatter albedo derived from light scattering and light absorption showed similar variation about the average value of 0.86 found by us during flights north of Barrow three years earlier during AGASP I.  相似文献   

6.
Rain and air of Florence have been collected in a continuous way andanalysed by flow analysis spectrofluorimetric methods for formaldehydeand hydrogen peroxide. Diurnal and seasonal variations were observed;the mean/maximum concentrations of all data (as gm–3) are 3.3/23.4 for HCHO and 0.4/4.93 forH2O2. The effect of external sources and ofphotochemical reactions produces periods of positive and negativecorrelations for these compounds. The mean/maximum rain concentration ofall data are 98/443 g l–1 for HCHO and 84/685 g l–1 for H2O2. Concentrationratios rain/air and discrepancies to Henry's Law equilibrium arediscussed.  相似文献   

7.
Weekly bulk aerosol samples collected at Funafuti, Tuvalu (8°30S, 179°12E), American Samoa (14°15S, 170°35W), and Rarotonga (21°15S, 159°45W), from 1983 through most of 1987 have been analyzed for nitrate and other constituents. The mean nitrate concentration is about 0.11 g m–3 at each of these stations: 0.107±0.011 g m–3 at Funafuti; 0.116±0.008 at American Samoa; and 0.117±0.010 at Rarotonga. Previous measurements of mineral aerosol and trace metal concentrations at American Samoa are among the lowest ever recorded for the near-surface troposphere and indicate that this region is minimally affected by transport of soil material and pollutants from the continents. Consequently, the nitrate concentration of 0.11 g m–3 can be regarded as the natural level for the remote marine boundary layer of the tropical South Pacific Ocean. In contrast, over the tropical North Pacific which is significantly impacted by the transport of material from Asia and North America, the mean nitrate concentrations are about three times higher, 0.29 and 0.36 g m–3 at Midway and Oahu, respectively. The major sources of the nitrate over the tropical South Pacific are still very uncertain. A very significant correlation between the nitrate concentrations at American Samoa and the concentrations of 210Pb suggests that transport from continental sources might be important. This continental source could be lightning, which occurs most frequently over the tropical continents. A near-zero correlation with 7Be indicates that the stratosphere and upper troposphere are probably not the major sources. A significant biogenic source would be consistent with the higher mean nitrate concentrations, 0.16 to 0.17 g m–3, found over the equatorial Pacific at Fanning Island (3°55N, 159°20W) and Nauru (0°32S, 166°57E). The lack of correlation between nitrate and nss sulfate at American Samoa does not necessarily preclude an important role for marine biogenic sources.  相似文献   

8.
Summary Regional climate model (RegCM2) and sulfur transport model (NJUADMS) were combined to simulate the distribution of anthropogenic sulfate aerosol burden over China, where a look up table method was applied to illustrate sulfate formation from SO2-oxidation. Direct radiative forcing of sulfate aerosol was further estimated using the scheme suggested by Charlson et al (1991). Investigations show that the annual average total sulfate column over mainland China is 2.01mg/m2 with high value in East and Central areas (more than 7mg/m2). The annual average direct radiative forcing of China is about –0.85W/m2. The forcing can reach –7W/m2 in Central and East China during the winter season. Total sulfate column shows significant seasonal variations with winter maximum-summer minimum in the Southern part of China and spring maximum-autumn minimum in the northern part of China. Strong seasonal cycles of direct radiative forcing are also found due to the influence of total sulfate column, cloud, relative humidity and the reflectivity of underlying surfaceReceived May 16, 2001; accepted August 5, 2002 Published online: May 8, 2003  相似文献   

9.
On the determination of the height of the Ekman boundary layer   总被引：1，自引：1，他引：1  
The heighth of the Ekman turbulent boundary layer determined by the momentum flux profile is estimated with the aid of considerations of similarity and an analysis of the dynamic equations. Asymptotic formulae have been obtained showing that, with increasing instability,h increases as ¦¦1/2 (where is the non-dimensional stratification parameter); with increasing stability, on the other hand,h decreases as –1/2. For comparison, a simple estimate of the boundary-layer heighth u determined by the velocity profile is given. As is shown, in unstable stratification,h u behaves asymptotically as ¦¦–1, i.e., in a manner entirely different from that ofh .  相似文献   

10.
Characterisation of the carbonate content of atmospheric aerosols   总被引：4，自引：0，他引：4  
A programme of aerosol sampling by dichotomous sampler has been undertaken with analysis of soluble ions plus carbonate. The technique for carbonate involved release of CO2 by HCl vapour and quantitative measurement of the CO2 by FTIR spectroscopy. The method is suitable for amounts down to below 10g CO3 2- per filter. The prevailing atmospheric levels in an urban area were found to be below 1g m-3. Information on the particle size from the dichotomous sampler was supplemented by use of a cascade impactor. Although CaCO3 is clearly the dominant species initial analyses demonstrated higher carbonate levels than could be accounted for on the basis of the concentrations of calcium and magnesium ions which are the most likely cations in mineral carbonates. Analysis with and without heating to 100°C in a vacuum oven demonstrates the presence of carbonate in volatile form. This could be due to carbon dioxide adsorbed onto particulate matter such as soot.  相似文献   

11.
Cloud water and interstitial aerosol samples collected at Mt. Sonnblick (SBO) were analyzed for sulfate and aerosol carbon to calculate in-cloud scavenging efficiencies. Scavenging efficiencies for sulfate (SO) ranged from 0.52 to 0.99 with an average of 0.80. Aerosol carbon was scavenged less efficiently with an average value (AC) of 0.45 and minimum and maximum values of 0.14 and 0.81, respectively. Both SO and AC showed a marked, but slightly different, dependence on the liquid water content (LWC) of the cloud. At low LWC, SO increased with rising LWC until it reached a relatively constant value of 0.83 above an LWC of 0.3 g/m3. In the case of aerosol carbon, we obtained a more gradual increase of AC up to an LWC of 0.5 g/m3. At higher LWCs, _ remained relatively constant at 0.60. As the differences between SO and A varied across the LWC range observed at SBO, we assume that part of the aerosol carbon was incorporated into the cloud droplets independently from sulfate. This hypothesis is supported by size classified aerosol measurements. The differences in the size distributions of sulfate and total carbon point to a partially external mixture. Thus, the different chemical nature and the differences in the size and mixing state of the aerosol particles are the most likely candidates for the differences in the scavenging behavior.  相似文献   

12.
Precipitation Chemistry in the Sahelian Savanna of Niger, Africa   总被引：1，自引：0，他引：1  
Within the framework of the IDAF (IGAC DEBITS AFRICA) network, we present in this paper data on precipitation and aerosol chemistry in the semiarid savanna of the Sahelian region of Niger. An automatic wet-only precipitation collector was operated at the Banizoumbou station during the entire 1996 rainy season (June to September 1996). Inorganic (Na+, NH 4 + , K+, Mg2+, Ca2+, Cl-, NO 3 - , SO 4 2- ) and organic contents of the precipitation (HCOOH, CH3COOH, C2H5COOH) were determined by Ion Chromatography (IC) in 29 rainfall events. Once per week, bulk particle samples were collected on the same site, and soluble water material was determined by IC. We examined the influence of atmospheric gas and particle sources on the precipitation and aerosol chemical contents. We established the influence of marine, terrigenous, and biogenic sources in the Sahelian region. The terrigenous signature is dominant and related to Sahelian soil erosion, with a high calcium content in precipitation (31.2 eq L-1) and in aerosols (1.8 g m-3). Two other signatures of atmospheric sources are highlighted by the relatively high nitrogenous (ammonium and nitrate) and organic contents (formate, acetate) in the precipitation. Ammonium (12.9 eq L-1) and nitrate (12.3 eq L-1) contents confirm respectively the biogenic source of ammonia released by domestic animal excreta in Niger and the natural emissions from semiarid savannas soils, perturbed by wild or domestic animal grazing. In spite of a high potential acidity given by nitrate, formate and acetate; a weak acidity (H+ (2.1 eq L-1) is calculated from the mean pH of 5.67 measured. A statistical analysis of the aerosol chemical composition clearly indicates that nitrates are strongly correlated at the 1% level with terrigenous ions, i.e., Ca2+ and Mg2+ (0.95 < r < 1). We observed a similar relationship between all the terrigenous ions and nitrate in the precipitation. In the Sahelian region, alkaline soil dust representative of the terrigenous contribution interact, with gaseous nitrogenous and carbonaceous compounds, leading to the neutralization of acid gases and subsequent weak acidity in precipitation. Finally, taking into account the main chemical characteristics of Banizoumbou precipitations and aerosols, which demonstrate the importance of heterogeneous and multiphase chemical processes, we propose a conceptual model of the atmospheric chemistry in the Sahelian region.  相似文献   

13.
Dimethylsulfide (DMS) in surface seawater and the air, methanesulfonic acid (MSA) and non-sea-salt sulfate (nss-SO4 2–) in aerosol, and radon-222 (Rn-222) were measured in the northern North Pacific, including the Bering Sea, during summer (13 July – 6 September 1997). The mean atmospheric DMS concentrations in the eastern region (21.0 ± 5.8 nmole/m3 (mean ± S.D.), n=30) and Bering Sea (19.9 ± 9.8 nmole/m3, n=10) were higher than that in the western region (11.1 ± 6.4 nmole/m3, n=31) (p<0.05), although these regions did not significantly differ in the mean DMS concentration in surface seawater. Mean sea-to-air DMS flux in the eastern region (21.0 ± 10.4 mole/m2/day, n=19) was larger than those in the western region (11.3 ± 16.9 mole /m2/day, n=22) and Bering Sea (11.2 ± 7.8 mole/m2/day, n=7) (p<0.05). This suggests that the longitudinal difference in atmospheric DMS was produced by that in DMS flux owing to wind speed, while the possible causes of the higher DMS concentrations in the Bering Sea include (1) later DMS oxidation rates, (2) lower heights of the marine boundary layer, and (3) more inactive convection. The mean MSA concentrations in the eastern region (1.18 ± 0.84 nmole/m3, n=35) and Bering Sea (1.17 ± 0.87 nmole/m3, n=13) were higher than that in the western region (0.49 ± 0.25 nmole/m3, n=28) (p < 0.05). Thus the distribution of MSA was similar to that of DMS, while the nss-SO4 2– concentrations were higher near the continent. This suggests that nss-SO4 2– concentrations were regionally influenced by anthropogenic sulfur input, because the distribution of nss-SO4 2– was similar to that of Rn-222 used as a tracer of continental air masses.  相似文献   

14.
Radiative Heat Transfer and Hydrostatic Stability in Nocturnal Fog   总被引：1，自引：0，他引：1  
We have performed a one-dimensional and transient radiative heat transfer analysis in order to investigate interaction between atmospheric radiation and convective instability within a nocturnal fog. The radiation element method using the Ray Emission Model (REM2), which is a generalized numerical method, in conjunction with a line-by-line (LBL) method, is employed to attain high spectral resolution calculations for anisotropically scattering fog. The results show that the convective instability has a strong dependence on radiative properties of the fog. For the condition of a 20-m droplet diameter and liquid water content of 0.1 × 10–3 kg m–3;, the temperature profile within the fog becomes S shaped, and a convective instability layer forms in the middle or lower level of the fog. However, for the same water content and a 40-m diameter droplet, no strong convective instability layer forms, whereas for a 10-m diameter droplet a strong convective instability is observed.  相似文献   

15.
The Petryanov air filters combined into half-year sets were analyzed for the presence of 40K, 137Cs and 22Na by means of low-background gamma rays spectrometry. Each sample contains aerosols from more than 1 Mm3 of air. Samples were collected in ground level air at Kraków (Southern Poland) from 1996 to 2002. Activity concentrations of 40K are almost constant with the mean of 14.7± 4.5 Bq m–3. Activity concentrations of 137Cs, which are on the level of single Bq m– 3 show exponential decrease with effective half-life time of 7.07± 0.77 years. The cosmogenic 22Na shows a strong seasonal variation with significant different mean values activity concentration between 0.333± 0.095 Bq m–3 and 0.137± 0.045 Bq m–3, for summer and winter, respectively. Moreover, the activity ratio for two cosmogenic radionuclides: 22Na and measured previously 7Be show also changes with statistically significant seasonal differences. The lower values were found during winters. The mechanisms which might govern this ratio are discussed. The conclusion is that transport of 22Na during summer seems to be so much effective, that results in kind of relative depletion of stratosphere of this nuclide.  相似文献   

16.
Although extensive areas of forests and grasslands are burned in the tropics, relatively little scientific attention has been focused on this phenomenon. In order to determine the land area burned and estimate the charcoal (elemental or graphitic carbon) produced, I monitored agricultural burning in a 1145 km2 area in central Panama during the 1981 dry season. Over 10% of the land surface was burned in that year. Charcoal concentrations in the aerosol were also measured and reached values of 3.1 gC/m3 during the peak in burning. Off-peak values of aerosol charcoal are less than 1 gC/m3. The high charcoal concentration reflects the massive amounts of vegetational burning occurring in the area.The charcoal advected by the air mass flowing over the area has been estimated using a box model. Assuming an average aerosol concentration of charcoal of 1 gC/m3 for a three-month burning period, a 2 km atmospheric mixed layer, a 14 km/h wind velocity to the south, and a 150 km wide zone across the western Gulf of Panama watershed, I estimate that, during the dry season, 9×109 g charcoal are mobilized by the troposphere. If 4.1×1012 g phytomass are annually burned in this region, then the charcoal emission factor to the troposphere is 2.2×10–3.  相似文献   

17.
Summary The relationships between smoke concentrations, measured at two monitoring stations in Athens by the ASTM (American Society for Testing and Materials) and the OECD (Organization for Economic Co-Operation and Development) methods are studied by using a sample of 738 mean daily values of simultaneous measurements during the period 1984–1986. It is shown that an exponential model, different for each monitoring station, with smoke concentrations in COH (coefficient of haze) as the independent variable and smoke concentrations in gr/m3 as the dependent variable, was the most appropriate for transforming smoke data from COH to gr/m3. Also it is shown that the transformation models can be applied independent of the prevailing meteorological conditions. Finally some tentative conclusions are derived concerning the long term variations of smoke concentrations in gr/m3 for the period 1977–1990 and 1973–1990 at the two monitoring stations respectively. The trend analysis has shown that pollution abatement efforts resulted in an about 10% per year decreasing trend in smoke concentrations, during the period 1986–1990, at these two Athenian stations.With 4 Figures  相似文献   

18.
With the aid of eddy correlation instrumentation, the components of the energy budget and CO2 flux were measured over grain sorghum grown at Mead, Nebraska. Diurnal patterns of sensible heat, latent heat, CO2 and momentum flux are examined for typical days. On a mostly clear day when the crop leaf area index was 3.7, net radiation reached a mid-day peak of 560 W m-2, while sensible and latent heat fluxes peaked at 50 and 460 W m-2, respectively. The peak CO2 flux occurring just prior to solar noon was 1.5 mg m-2(ground area) s-1. CO2 flux (respiration from plants, soil and roots) in the early evening was about -0.28 mg m-2 (ground area) s-1.A relationship between CO2 flux and photosynthetically active radiation (PAR) was developed. Except during the late stage of growth (growth stage 8.5, toward the initiation of senescence), the crop showed no evidence of saturation up to PAR 1800 Ei m-2s-1. The light compensation point was found to be about 211 Ei m-2s-1. Examination of CO2 flux-PAR relationships for selected days through the season indicated an aging effect in terms of a decrease in photosynthetic activity of the sorghum canopy. Measurements made on two consecutive days demonstrate the effects of weather conditions on CO2 flux and carbon-water flux ratio (a measure of water use efficiency of the crop). The occurrence of regional sensible heat advection with concommitant high vapor pressure deficit and air temperature-limited CO2 exchange reduced the carbon-water flux ratio.Published as Paper No. 7717, Journal Series, Nebraska Agricultural Research Division. The work was conducted under Regional Research Project 11-33 and Nebraska Agricultural Research Division Project 27-003.Formerly Post Doctoral Research Associate (now at the University of Connecticut Department of Renewable Natural Resources Storrs CT)  相似文献   

19.
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.  相似文献   

20.
Airborne measurements made during August 1985 over Greenland and its environs show that both accumulation-mode (0.1 m D2.0 m) and giant (D2 m) particles were present in relatively high concentrations in arctic haze layers and that the accumulation-mode particles dominated light scattering. Particles with diameters (D) between 1 and 4 m consisted predominately of mixed materials, small and dense inclusions, and probably organic compounds containing sulfur. Many of the particles from 0.1 to 1 m in diameter were also of mixed composition, with sulfuric acid, ammonium sulfate and organics probably the dominant constituents.  相似文献   

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