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1.
Measurements of fog and rain water chemistry at the summit of Mt. Fuji, the highest peak in Japan, as well as at Tarobo, the ESE slope of Mt. Fuji in September 2002. The pH of fog and rain water sampled at Mt. Fuji varied over a range of 4.0–6.8. Acidic fogs (pH < 5.0) were observed at the summit when the air mass came from the industrial regions on the Asian continent. The ratio of [SO42−]/[NO3−] in the fog water was lower at Tarobo than at the summit. High concentrations of Na+ and Cl− were determined in the rain water sampled at the summit, possibly because of the long-range transport of sea-salt particles raised by a typhoon through the middle troposphere. The vertical transport of sea-salt particles would influence the cloud microphysical properties in the middle troposphere. Significant loss of Mg2+ was seen in the rain water at the summit. The concentrations of peroxides in the fog and rain water were relatively large (10–105 μM). The potential capacity for SO2 oxidation seems to be strong from summer to early autumn at Mt. Fuji. The fog water peroxide concentrations displayed diurnal variability. The peroxide concentrations in the nighttime were significantly higher than those in the daytime.  相似文献   

2.
Measurements on drop size were made in cumulus clouds over Pune (inland region) during the summer monsoon seasons. In this paper, the measurements of the cloud drop spectra made in non-raining clouds at different levels and for different thickness have been studied. Also, those on the days with rain and with no rain (the rain being observed within the clouds) have been compared. The average spectra broadened with height. The concentration of drops >50 μm (NL), liquid water content (LWC), mean volume diameter (MVD) and dispersion increased with height. The concentration of drops <20 μm (NS) and total concentration (NT) decreased with height. The spectra were broader, while NS and NT are smaller and the other parameters are greater for thicker clouds as compared to those for thinner. The spectra were broader, while NS and NT are smaller and the other parameters are greater on the days with rain with respect to those on the days with no rain. The distributions were bimodal at higher levels, for thicker clouds and on the days with rain, while they were unimodal at lower levels, for thinner clouds and on the days with no rain. The variations of the cloud drop spectra, preceding rain, at initial stage of rain and following rain are discussed.  相似文献   

3.
The concentrations of H+, nitrate (NO3 -), and sulfate (SO4 2-) in rainwater and their temporal changes were analyzed on the basis of continuous observation from 1 July 1991 to 30 June 1992 at a suburb of Nagoya, Japan. The yearly average for pH was 4.4. In general, an increasing pH with increase in precipitation amount was observed for rain events. Relatively high pH rainwater was sometimes observed at the beginning of rainfall, even though high concentrations of NO3 - and SO4 2- were involved. The high pH values were considered to be caused by the neutralization process with particulate matter containing cations. The yearly averaged ratio of equivalent concentration of nitrate to sulfate (N/S) in rainwater was 0.58. In the early stage of rain, the N/S value was usually more than 1.0 due to the difference of scavenging process between NO3 - and SO4 2-. High values of N/S ranging from 5 to 10 were found under the atmospheric conditions of calm winds and low humidity, during which it is possible that atmospheric particles float for a long time in the air before a rain event. The adsorption of NO3 - in the early stage of rainfall by particulate matter was suggested from the difference in scavenging processes of NO3 - and SO4 2-. A possible scavenging process, called limb cloud scavenging, is presented to explain the interaction of particles and nitrate ions at the early stage of rain. In limb cloud scavenging, the repeated migration of cloud particles or raindrops between the inside and outside of clouds increases the absorption of ions to a highly condensed level, thus increasing the N/S value of rainwater. The influence of global scale seasonal phenomena with large amounts of particulates, such as typhoons or Asian dust storms, was also studied.  相似文献   

4.
By making use of TOVS Path-B satellite retrievals and ECMWF reanalyses, correlations between bulk microphysical properties of large-scale semi-transparent cirrus (visible optical thickness between 0.7 and 3.8) and thermodynamic and dynamic properties of the surrounding atmosphere have been studied on a global scale. These clouds constitute about half of all high clouds. The global averages (from 60°N to 60°S) of mean ice crystal diameter, De, and ice water path (IWP) of these clouds are 55 μm and 30 g m−2, respectively. IWP of these cirrus is slightly increasing with cloud-top temperature, whereas De of cold cirrus does not depend on this parameter. Correlations between De and IWp of large-scale cirrus seem to be different in the midlatitudes and in the tropics. However, we observe in general stronger correlations between De and IWP and atmospheric humidity and winds deduced from the ECMWF reanalyses: De and IWP increase both with increasing atmospheric water vapour. There is also a good distinction between different dynamical situations: In humid situations, IWP is on average about 10 gm−2 larger in regions with strong large-scale vertical updraft only that in regions with strong large-scale horizontal winds only, whereas the mean De of cold large-scale cirrus decreases by about 10 μm if both strong large-scale updraft and horizontal winds are present.  相似文献   

5.
A total of 48 precipitation samples have been collected from individual precipitation events at the Nam Co Monitoring and Research Station for Multisphere Interactions (Nam Co Station, 30°47′N, 90°58′E; 4730 m a.s.l) located in the central Tibetan Plateau from August 2005 to August 2006. All samples were analyzed for major cations (NH4+, Na+, K+, Ca2+ and Mg2+) and anions (Cl−, NO3− and SO42−), conductivity and pH. Precipitation pH values ranged from 6.03 to 7.38 with an average value of 6.59. The high pH is due to large inputs of crustal aerosols in the atmosphere, which contain a large fraction of carbonate. Ca2+ is the dominant cation in precipitation with an average value of 65.58 μeq L− 1 (4.91–301.41 μeq L− 1), accounting for 54% of the total cations in precipitation. HCO3− is the predominant anion, accounting for 62% of the total anions. When compared with data from a snow pit in the Zhadang Glacier 50 km away (5800 m a.s.l), major ion concentration in precipitation at the Nam Co Station is much higher due to local aerosol inputs. Correlation and empirical orthogonal function (EOF) analysis indicate that regional crustal aerosols and species from combustion emissions of residents are the major sources for these ions, lake salt aerosols from the Nam Co nearby and regional mineral aerosols from dry lake sediments are secondary sources, and sea salt contribution is the least due to the long distance transport.  相似文献   

6.
Volatile organic compounds (VOCs) emissions by vegetation present in the Mediterranean area are not well known. They may contribute with anthropogenic VOC emissions to the tropospheric ozone formation that reaches important level in the European Mediterranean region. The present work, carried out as part of the European ESCOMPTE project «fiEld experimentS to COnstrain Models of atmospheric Pollution and Transport of Emissions», adds a new contribution to the inventory of the main natural hydrocarbons sources likely to participate in the ozone production. The corresponding measurement campaign was conducted in La Barben, a site close to Marseilles (France), with the aim to quantify the terpenic emission pattern and the behaviour of Pinus halepensis, an important Mediterranean species slightly studied.The determination of biogenic emissions from P. halepensis was done by the enclosure of an intact branch in a Teflon cuvette. Main emitted monoterpenes were β trans-ocimene and linalool. The total monoterpenic emission rates thus recorded were found to reach maximum values around 30 μg gdry weight−1 h−1. The normalized emission rates calculated at 30 °C and 1000 μmol m−2 s−1 with Guenther's algorithm was 14.76, 8.65 and 4.05 μg gdry weight−1 h−1, respectively, for the total monoterpenes, β trans-ocimene and linalool.  相似文献   

7.
The effects of below-cloud aerosol on the acidification process of rain   总被引：1，自引：0，他引：1  
Using a model of the acidification process of rain, we calculate and analyze the effects and contributions of a below-cloud aerosol in its different concentrations and acidities on the pH and ion components of rain (SO 4 2– , H+, NO 3 – , NH 4 + , etc.) under the conditions of different concentrations of pollution gases. The results show that the aerosol has an acidification or alkalization effect on the rain which changes the pHs of rain and aerosol. As acidifying pollution gas concentrations (SO2, HNO3) are low, the acid aerosol has important effects on the pH and H+ of rain, but as the gas concentrations are high, the acid aerosol has very little effect. The alkalizing aerosol makes the pH of rain increase by between 0.3 and 0.5 and neutralizes about 60% of H+ in the rain. As alkalizing pollution gas NH3 exists, the acid aerosol has important effects on the pH and H+ of rain. But the alkalizing aerosol has very little effect, especially as the NH3 concentration is high. The percentage contribution of the aerosol to SO 4 2– in rain is generally 7–15%, the contribution of the aerosol to NO 3 – is nearly the same as that of HNO3=1 ppb, and the contribution of the aerosol to NH 4 + is nearly the same as that of NH3, from 5 to 7 ppb, and is an important source of NH 4 + in rain. Finally, according to the actual conditions of typical regions in the south and north of China (Chongqing and Beijing), we analyze the effects of aerosol and pollution gases on the ion components of rain.  相似文献   

8.
This paper reports the results of a study on the transformation of benzene in the presence of solid nitrate salts (NaNO3, NH4NO3) under irradiation in a gas-solid photoreactor. Sodium and ammonium nitrate have been chosen as representative of the composition of atmospheric particulate, benzene as a model aromatic molecule. The purpose is to simulate the transformations that aromatic compounds undergo on the surface of dispersed particles in the atmosphere. Irradiation of sodium nitrate causes hydroxylation and nitration of benzene, yielding phenol and nitrobenzene. This is most likely due to the generation of •OH and •NO2 radicals upon nitrate photolysis, with •OH + O2 leading to the formation of phenol and •OH + •NO2 yielding nitrobenzene. The percentage of oxygen in the reaction environment influences the transformation pathways, with phenol formation being favoured and nitrobenzene formation depressed by high O2 concentration. In the presence of hematite (α-Fe2O3, another component of atmospheric particulate) very relevant formation of nitrobenzene takes place even with 21% oxygen (simulated air), indicating that the interaction between hematite and nitrate can lead to the formation of aromatic nitroderivatives on the surface of atmospheric particulate. The effect of hematite is possibly due to protonation of peroxynitrite, formed upon nitrate photoisomerisation, to peroxynitrous acid, a powerful nitrating agent. A similar effect leads to relevant formation of nitrobenzene under atmospheric conditions upon irradiation of the acid salt ammonium nitrate.  相似文献   

9.
PM10 and heavy metal measurements in an industrial area of southern Italy   总被引：1，自引：0，他引：1  
Atmospheric particulate concentrations and heavy metal content are measured from March to July 2001 at an industrial site located in a rural zone of the southern Italy. PM10 samples are collected by a low-volume sampler and each sample is analysed by AAS techniques for its content of Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn. We measure also temperature, atmospheric pressure and relative humidity, and we collect anemometric data. The study purpose is the investigation of pollutant levels in an industrial area located in a rather unpolluted region and the characterization of the correlation structure among particulate concentrations, heavy metal content and local meteorological parameters. Data analysis is carried out by means of univariate and multivariate statistical methods. In the investigated period, the average value of PM10 daily concentrations (24 μg Nm− 3) does not exceed the national standard of 40 μg Nm− 3 and only nine values are higher than the European daily limit value of 50 μg Nm− 3. Particularly, the occurrence of two anomalous values (183 μg Nm− 3 in 3 March and 94 μg Nm− 3 in 22 June) seems to be related to no-local events as confirmed both by in situ data measured in the AQM network of Potenza city (about 10 km far from the study area) and by remote measurements performed in the same days. Regarding the heavy metal levels, we observe high levels of Cr (34 ng Nm− 3), Ni (85 ng Nm− 3) and Zn (214 ng Nm− 3) in agreement with the local industrial source pattern. The multivariate analysis, carried out using meteorological parameters as exogenous variables, allow to evaluate the role of the different variables as driving factors of the correlation structure among the metals.  相似文献   

10.
The absorption cross-sections of HCFC-123 (CF3–CHCl2), HCFC-141b (CH3–CFCl2) and HCFC-142b (CH3–CF2Cl) are measured between 170 and 250 nm for temperatures ranging from 295 to 210 K with uncertainties between 2 and 4%. They are compared with other available determinations. Temperature effects are discussed and parametrical formulae are proposed to compute the absorption cross-section for wavelengths and temperatures useful in atmospheric modelling calculations. Photodissociation coefficients are presented and their temperature-dependence is discussed.  相似文献   

11.
We have analyzed the fine-structure of 131 electric field (E) waveforms that were radiated during the onset of first return strokes in cloud-to-ocean lightning. The dE/dt waveforms were recorded using an 8-bit waveform digitizer sampling at 100 MHz, and the E waveforms were sampled at 10 MHz using a 10-bit digitizer. 49 (or 37%) of the dE/dt waveforms contain one or more large pulses within ± 1 μs of the largest (or dominant) peak in dE/dt, i.e. within an interval from − 1 μs to + 1 μs, where t = 0 μs is the time of the dominant peak, and 37 (or 28%) have one or more large pulses in the interval from 4 μs before to 1 μs before the dominant peak, i.e. − 4 μs to − 1 μs, and only the dominant peak within ± 1 μs . We give statistics on the amplitude and timing of dE/dt pulses that are near the dominant peak, and we show how the presence of these pulses adds considerable fine-structure to the shape of Eint, the integrated dE/dt waveform, on a time-scale of tens to hundreds of nanoseconds. This fine-structure includes fast pulses near the beginning of the slow front, large pulses and shoulders within the slow front and during the fast-transition, and very narrow peaks in Eint. Our overall conclusion is that the electromagnetic environment near the point(s) where lightning leaders attach to the surface is often more complicated than what would be produced by a single current pulse propagating up a single channel at the time of onset.  相似文献   

12.
In November 2004–January 2005, a micro orifice uniform deposit impactor (MOUDI) and a Nanometer (nanometer)-MOUDI were used in the center of Taiwan to measure particle size (18 nm particle size 18 μm) distributions of atmospheric aerosols at a traffic site during the winter period. The average Mass in Media Aerodynamic Diameter (MMAD) of suspended particles is 0.99 μm this study. As for the ultra fine and nanometer (nanometer) particle mode, the composition order for these major ions species was SO42− NH4+ NO3− Mg2+ Ca2+ Na+ K+ Cl−. An ion Chromatography (DIONEX-100) was used to analyze major anion species, Cl−, NO3−, SO42− and cation species, NH4+Na+, K+, Ca2+Mg2+. Their concentrations were also extracted from various particles size modes (nanometer (nanometer), ultra fine, fine and coarse). The results obtained in this study also indicated that the average portions for the major ionic species (SO42−, NH4+ and Mg2+) in the nanometer (nanometer), ultra fine, fine and coarse particulate modes are about 34%, 37%, 63% and 30%, respectively at this traffic sampling site during the winter period.  相似文献   

13.
Data concerning carbon cycle variations on the earth's surface during the past 200,000 years are reviewed.The variations of the surface temperature (T) and concentration of carbon dioxide (CO2) in the atmosphere of Antarctica are compared to those of the isotopic ratios of oxygen 18O/16O (δ18O) and of carbon 13C/12C (°13C) of waters in the deep oceans for the two last glacial cycles. This comparison shows that the decrease of the atmospheric CO2 concentration is accompanied by a carbon transferase from the continental biosphere to the oceanic deep waters. At the glacial maximum this transfer is estimated to be about 500 GtC (1 GtC = 1015g of carbon) equivalent to 25% of the carbon storage of the biosphere. It occurs mainly in the high latitudes of the Southern Hemisphere by incorporation of CO2 into particulate matter during photosynthesis. It is shown that the mean oceanic productivity does not increase with a supplementary supply of ions such as phosphate (PO43−) or nitrate (NO3−) but that the intensity of the thermohaline circulation is certainly reduced. As the warming up of the oceans and the melting of the ice-sheet begin carbon transfer takes place to restore the continental biosphere.Another carbon transfer of a much more important intensity is also at work in the sea shore environment. Its intensity could be sufficient to renew the entire carbon of the continental biospheric, atmospheric and oceanic reservoirs in a length of time comparable to a glacial cycle. This fact shows the importance of studying the deposition of carbon in oceanic zones which are uncovered with drops in sea level. At the present time data on the coastal environment in relation to the global carbon cycle are very scarce and warrants more research in this area.  相似文献   

14.
The changing chemical composition of cloud water and precipitation in the Western Sudety Mountains are discussed against the background of air-pollution changes in the Black Triangle since the 1980s until September 2004. A marked reduction of sulphur dioxide emissions between the early 1990's and the present (from almost 2 million tons to around 0.2 million tons) has been observed, with a substantial decline of sulphate and hydrogen concentration in cloud water (SO42− from more than 200 to around 70 μmol l− 1; H+ from 150 to 50 μmol l− 1) and precipitation (SO42− from around 80 to 20–30 μmol l− 1; H+ from around 60 to 10–15 μmol l− 1) samples. At some sites, where fog/cloud becomes the major source of pollutants, deposition hot spots are still observed where, for example, nitrogen deposition can exceed 20 times the relevant critical load. The results show that monitoring of cloud water chemistry can be a sensitive indicator of pollutant emissions.  相似文献   

15.
The present study was carried out between October 2003 and September 2004 at an urban background station near the Mediterranean coast in southeastern Spain. The sulfate and nitrate content was determined in 332 PM10 and PM2.5 daily samples. The results show that the seasonal variation of nitrate measured in PM10 does not correspond with what has been observed at other locations in the Iberian Peninsula, where the minima are reached during the summer months due to decomposition of ammonium nitrate at high temperatures. The recorded levels of PM10 nitrate were slightly higher in summer due to an increase in the concentrations of coarse mode nitrate. On the contrary, both the concentrations and the percentages of nitrate in PM2.5 were lowest from June to September. The sulfate levels in both PM10 and PM2.5 were maxima in summer because the oxidation rate of SO2 increases with solar radiation. An elevated correlation (0.72 < r < 0.92) between the monthly average concentrations and percentages of sulfate and solar radiation has been found. We have also investigated the influence that Saharan dust intrusions and high pollution episodes have upon the sulfate and nitrate concentrations. Both types of events increased NO3− and SO42− levels, particularly the high pollution episodes.  相似文献   

16.
The pH and the concentrations of sulfate, nitrate, ammonia, and calcium in rainwater were measured for two periods of a single midwest rainstorm which occurred over a mesometeorological network in central Illinois on 24–25 July 1979. Regression analysis was used to compare ion concentrations with rainfall amount, and ion balance was used to compare cation and anion concentrations at individual sites. Only the ions SO4 2- and NO3 - show any significant relationship to rainfall amount, decreasing as rainwater amounts increase (r=–0.57 and –0.60, respectively). During the first period of the rainstorm, a sequential sampler measurements allowed the calculation of detailed temporal variations in SO4 2-, pH, and rain rate. SO4 2- decreased, and pH increased as the rate increased and the opposite temporal pattern occurred as the rain decreased at the end of the period. Reasons for these variations are discussed.Research done while a visiting scientist at the Illinois State Water Survey, Champaign, Illinois, U.S.A.  相似文献   

17.
The solubilities and hydrolysis rates of PAN (peroxyacetyl nitrate) and its homologues PPN (peroxypropionyl nitrate), PnBN (peroxy-n-butyl nitrate), PiBN (peroxy-isobutyl nitrate) and MPAN (peroxymethacryloyl nitrate) in liquid water have been studied at 20 °C. Temperature dependencies were measured for PAN and PPN. The solubilities of peroxyacyl nitrates decrease smoothly with increasing carbon-chain length fromH (293 K)=4.1 M atm–1 (PAN) toH (293 K)=1.0 M atm–1 (PiBN). Hydrolysis-rate constants, which cover the range fromk h (293 K)=(2.4–7.4)×10–4 s–1, do not show a systematic chain-length dependency. Solubilities of PAN and PPN in solutions which mimic the composition and ionic strength of sea water are 15% and 20% lower than in pure water. The hydrolysis rate constants are not affected.  相似文献   

18.
The main objective of this study is to investigate the chemical characteristics of biomass burning aerosol and its impact on regional air quality during an agricultural waste burning period in early summer in the rural areas of Korea. A 12-h integrated intensive sampling of biomass burning aerosol in the fine and coarse modes was conducted on 2–20 June 2003 in Gwangju, Korea. The collected samples were analyzed for concentrations of mass, ionic, elemental, and carbonaceous species. Average concentrations of fine and coarse mass were measured to be 67.9 and 18.7 μg m− 3 during the biomass burning period, 41.9 and 18.8 μg m− 3 during the haze period, and 35.6 and 13.3 μg m− 3 during the normal period, respectively. An exceptionally high PM2.5 concentration of 110.3 μg m− 3 with a PM2.5/PM10 ratio of 0.79 was observed on 6 June 2003 during the biomass burning period. The potassium ratio method was used to identify biomass burning samples. The average ratio of potassium in the fine mode to the coarse mode (FK/CK) was 23.8 during the biomass burning period, 6.0 during the haze period, and 4.7 during the normal period, respectively. A FK/CK ratio above 9.2 was considered a criterion for biomass burning event in this study. Particulate matter from the open field burning of agricultural waste has an adverse impact on visibility, human health, and regional air quality.  相似文献   

19.
Aerosol mass size distribution has been measured by using an optical particle counter. The measurements were done in an urban background location in the western Mediterranean during winter 2006. The study has been focused in determining the mass size distribution under special meteorological conditions like moderate rain, considerable winds and high atmospheric stability. The results obtained showed a mass predominance of accumulation mode during rain and high stability periods although for different reasons. In the case of rain, it is due to greater atmospheric cleansing effectiveness that rain has upon coarse mode particles. However, during stagnant periods, the meteorological situation favored coagulation processes among nucleation mode particles giving like result a mass increase in the accumulation mode. Finally, strong winds favor the resuspension of the largest particles and the dispersion of particles with sizes inferior to 7.5 μm. Similar results have been reproduced using principal component analysis (PCA). In this way, three components were identified. The first (PC1) represents particles in the accumulation mode. The second component (PC2) is constituted by coarse particles to 7.5 μm, and the third (PC3) corresponds to coarser particles. The contribution of each group to the overall average concentration was determined: 27.2% corresponds to particles with sizes belonging within the first component, 35.4% to PC2 and 37.3% to PC3. Important percentage variability for each component under meteorological episodes has been obtained. Results obtained showed an important increase of PC1 during Rainy Days (53.8%) and High Pollution Days (40.2%). Contrary to this on Windy Days this component decreases to 7.4%. However, during this kind of day PC3 increases to 64.6%.  相似文献   

20.
A partial balance of mineral N is given for the basins of two coastal rivers in a forest zone in the Ivory Coast. The dry and wet depositions on the basin surfaces is given for particulate matter (NO3 –, NH4 +). The quantity of mineral N washed away in the rivers is evaluated. The losses from leaching of the soils by rainwater are about 0.33 to 1.0% of the atmospheric depositions for NH4 +–N and 2.2 to 5.8% for NO3 ––N. The yearly atmospheric input of N compounds to the ecosystem, about 1.4 g N m–2 y–1, is at least 14% of mineral N formed in the soils and is therefore quite significant.  相似文献   

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