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1.
南京冬季辐射雾和平流辐射雾的化学特征差异   总被引：1，自引：0，他引：1  
利用2006和2007年冬季南京雾外场试验中取得的雾水离子成分资料,分析了雾水化学组分特征,探讨了雾水酸度来源及辐射雾和平流辐射雾的化学特征差异。结果表明,南京冬季雾水中总离子浓度偏高,浓度最高的3种离子成份是SO^-24、NH^＋4和Ca^2＋,但雾水酸性不强,碱性离子成分的中和作用是pH值较高的原因。平流辐射雾中雾水离子总浓度约为辐射雾的2.2倍,平流辐射雾中浓度最高的阳离子为NH^＋4,辐射雾中为Ca^2＋。  相似文献   

2.
The deposition fluxes of inorganic compounds dissolved in fog and rain were quantified for two different ecosystems in Europe. The fogwater deposition fluxes were measured by employing the eddy covariance method. The site in Switzerland that lies within an agricultural area surrounded by the Jura mountains and the Alps is often exposed to radiation fog. At the German mountain forest ecosystem, on the other hand, advection fog occurs most frequently. At the Swiss site, fogwater deposition fluxes of the dominant components SO42− (0.027 mg S m−2 day−1), NO3− (0.030 mg N m−2 day−1) and NH4+ (0.060 mg N m−2 day−1) were estimated to be <5% of the measured wet deposition (0.85, 0.70 and 1.34 mg m−2 day−1, respectively). The corresponding fluxes at the forest site (0.62, 0.82 and 1.16 mg m−2 day−1, respectively) were of the same order of magnitude as wet deposition (1.04, 1.01 and 1.36 mg m−2 day−1), illustrating the importance of fog (or occult) deposition. Trajectory analyses at the forest site indicate significantly higher fogwater concentrations of all major ions if air originated from the east (i.e. the Czech Republic), which is in close agreement with earlier studies.  相似文献   

3.
Processing of atmospheric organic matter by California radiation fogs   总被引：2，自引：0，他引：2  
Considerable effort has been put into characterizing the ionic composition of fogs and clouds over the past twenty-five years. Recently it has become evident that clouds and fogs often contain large concentrations of organic material as well. Here we report findings from a series of studies examining the organic composition of radiation fogs in central California. Organic compounds in these fogs comprise a major fraction of total solute mass, with total organic carbon sometimes reaching levels of several tens of mg/L. This organic matter is comprised of a wide variety of compounds, ranging from low molecular weight organic acids to high molecular weight compounds with molecular masses approaching several hundred to a thousand g/mole. The most abundant individual compounds are typically formic acid, acetic acid, and formaldehyde. High concentrations are also observed of some dicarboxylic acids (e.g., oxalate) and dicarbonyls (e.g., glyoxal and methylglyoxal) and of levoglucosan, an anhydrosugar characteristically emitted by biomass combustion. Many other compounds have been identified in fog water by GC/MS, including long chain n-alkanoic acids, n-alkanes, PAH, and others, although these compounds typically comprise a total of only a few percent of fog TOC. Measurements of fog scavenging of organic and elemental carbon reveal preferential scavenging of organic carbon. Tracking of individual organic compounds utilized as source type markers suggests the fogs differentially scavenge carbonaceous particles from different source types, with more active processing of wood smoke than vehicle exhaust. Observations of high deposition velocities of fog-borne organic carbon, in excess of 1 cm/s, indicate that fogs in the region represent an important mechanism for cleansing the atmosphere of pollution.  相似文献   

4.
We have recently set up a new procedure for characterising the water soluble organic compounds (WSOC) in fog water, for which information is still rather limited. Fog samples collected during the 1998–1999 fall–winter season in the Po Valley (Italy) were analysed following this procedure, which allows a quantitative determination of three main classes of organic compounds (neutral species, mono- and di-carboxylic acids, polycarboxylic acids), together accounting for ca. 85% of the total WSOC. This procedure also provides information on the main chemical characteristics of these three classes of compounds (functional groups, aliphatic vs. aromatic character, etc.). The enhanced chemical knowledge on fog/cloud chemical composition opens new scenarios as far as chemical and microphysical processes in clouds and fogs are concerned.  相似文献   

5.
Two almost identical eddy covariance measurement setups were used to measure the fogwater fluxes to a forest ecosystem in the “Fichtelgebirge” mountains (Waldstein research site, 786 m a.s.l.) in Germany. During the first experiment, an intercomparison was carried out with both setups running simultaneously at the same measuring height on a meteorological tower, 12.5 m above the forest canopy. The results confirmed a close agreement of the turbulent fluxes between the two setups, and allowed to intercalibrate liquid water content (LWC) and gravitational fluxes. During the second experiment, the setups were mounted at a height of 12.5 and 3 m above the canopy, respectively. For the 22 fog events, a persistent negative flux divergence was observed with a greater downward flux at the upper level. To extrapolate the turbulent liquid water fluxes measured at height z to the canopy of height hc, a conversion factor 1/[1+0.116(z−hc)] was determined. For the fluxes of nonvolatile ions, no such correction is necessary since the net evaporation of the fog droplets appears to be the primary cause of the vertical flux divergence. Although the net evaporation reduces the liquid water flux reaching the canopy, it is not expected to change the absolute amount of ions dissolved in fogwater.  相似文献   

6.
Differences in total iron and manganese concentrations between large (d > 23 m) and small (4 < d < 23 m) cloud and fog drops were investigated at four locations in the United States. The study examined coastal stratus and stratocumulus clouds in southern California and northern Oregon, frontal and orographic clouds at Mt. Mitchell, North Carolina, and radiation fogs in California's San Joaquin Valley. The speciation of iron as a function of drop size was also examined in some fog samples from the San Joaquin Valley. Total iron and manganese concentrations were generally higher in large drops than in small drops in clouds sampled at Mt. Mitchell and along the southern California coast. These species were typically enriched in small drops at the Oregon coast and San Joaquin Valley sites. Ratios of dissolved Fe(III) to total dissolved Fe ranged from 0.88 to 0.93 in small fog drops. Non-uniform distributions of iron and manganese across the drop size spectrum can influence rates of metal catalyzed S(IV) autooxidation. Approximately 50% of the sampled clouds were calculated to experience autooxidation rate enhancements greater than 30% due to variations in drop acidity and catalyst concentrations with drop size.  相似文献   

7.
In order to determine if pollutants from the Wollongong-Sydney-Newcastle industrial area in southeastern Australia can be transported northwards, affecting precipitation quality to the north, a preliminary study of fog and rainwater quality was carried out from January to April 1989. Samples were collected from two sites in the state of New South Wales, one in the Barrington Tops and the other near Dorrigo. These samples were analyzed for the cations sodium, calcium, magnesium, potassium, and ammonium, and the anions chloride, nitrate, sulfate, methanesulfonate, formate and acetate, as well as pH and conductivity.The mean pH of fogwater from the two sites was 5.48, compared to 5.62 for rainwater. Fogwater also had concentrations of ions 2–6 times those in rainwater. For both fog and rain the ions sodium, chloride, magnesium, and methanesulfonate at both sites were essentially entirely sea-salt derived, while only 5–50% of potassium, calcium, and sulfate were derived from sea-salt. The acid-base balance was adequately described (r=0.76) by a balance between the acidity contributed by sulfuric and nitric acids, neutralized by the alkalinity of ammonia and (soil dust-derived) calcium carbonate. Comparing this study with others, both within Australia and overseas, fog and rainwater at both sites are not polluted, with acidity only slightly greater than background and concentrations of anthropogenic pollutants very low, and with sea-salt influences accounting for the majority of ionic loading.  相似文献   

8.
Nitrite oxidation in the tropospheric aqueous phase by freezing was evaluated by freezing a field sample. Nitrite oxidation by dissolved oxygen in the freezing process is much faster than by other oxidation processes, such as reactions with ozone, hydrogen peroxide or dissolved oxygen in an aqueous solution at pHs 3 to –6. At pH 4.5 and 25°C, the lifetime of nitrite in the aqueous phase is ca. 1 hr in oxidation by ozone (6×10-10 mol dm-3), ca. 10 hr in oxidation by H2O2 (2×10-4 mol dm-3), and 7.5 hr (Fischer and Warneck, 1996) in photodissociation at midday in summer. Under the same conditions at a temperature below 0°C, the lifetime of nitrite in the freezing process is estimated as ca. 2 sec when the droplets are frozen within a second. The reaction by freezing is affected by the presence of salts, such as NaCl or KCl, or orgnaic compounds, such as methanol or acetone. The results of freezing a field rain or fog sample showed that nitrite oxidation proceeds below pH 6, and the conversion ratio of nitrate from nitrite increases with decreasing pH. The oxidation of nitrite by freezing was also observed in freezing fog particles generated by an ultrasonic humidifier. The ratios of the concentrations of ions in the winter sample to those in the summer sample (or those in the fog sample) were almost the same values. However, the concentration of nitrite in the winter sample was lower than that estimated by the ratios of other ions. From the present study, it seems that the freezing process plays an important role in the nitrite sink process in the tropospheric aqueous phase.  相似文献   

9.
The indoor PM2.5 aerosol samples for charcoal broiling source under Chinese traditional charbroiling and the ambient fine aerosols samples (PM2.5) were collected in Beijing to investigate the characteristics of the charcoal broiling source and its impact on the fine organic aerosols in the atmosphere. The concentrations of 20 species of the trace organic compounds, including polycyclic aromatic hydrocarbons (PAHs), fatty acids, levoglucosan, and cholesterol in PM2.5 were identified and quantified by GC/MS. The total PAHs and fatty acids emitted from charcoal broiling to PM2.5 were 8.97 and 87,000 ng mg−1 respectively. The concentrations of the light molecular weight (LMW) 3- and 4-ring PAHs were much higher than those of the high molecular weight (HMW) 5- and 6-ring PAHs. Fatty acids were the most abundant species in source profile, accounting for over 90% of all identified organic compounds. More polyunsaturated fatty acid (linoleic acids) than the saturated fatty acid (stearic acids) emitted in the cooking. Charcoal broiling is a minor source of PAHs compared to the source of biomass burning. Comparing the ratios of levoglucosan/fatty acid and levoglucosan/cholesterol in the charcoal broiling samples to the ambient samples, it is evident that meat cooking is an important source of fatty acids, but a less important source of cholesterol. Cooking, as one of the source of fine organic particles, plus other anthropogenic sources would be related to the formation of the severe haze occurred and spread over the urban atmosphere in most of the cities of China in the past several years.  相似文献   

10.
The fog meteorology, fog chemistry and fog deposition on epiphytic bryophytes were investigated from July 2000 to June 2001 in the Yuanyang Lake forest ecosystem. The elevation of the site ranges from 1650 to 2420 m, at which the high frequency of fog occurrence throughout the year has been thought to be of benefit to the establishment of the primary Taiwan yellow cypress forest [Chamaecyparis obtusa var. formosana (Hayata) Rehder] and to the extensive growth of the epiphytic bryophytes. A weather station including a visibility sensor and an active fog collector was installed for fog meteorological and chemical study. The fog deposition rate on epiphytic bryophytes was estimated by measuring the increase rate in plant weight when exposed to fog. Average fog duration of 4.7 and 11.0 h per day was measured in summer months (June to August) and the rest of the year, respectively. November 2000 was the foggiest month in which the average fog duration reached 14.9 h per day. The ionic composition of fog water revealed that the area was less polluted than expected from literature data. The in situ exposure experiments done with the dominant epiphytic bryophytes showed an average fog deposition rate of 0.63 g H2O g−1 d. w. h−1, which approximated 0.17 mm h−1 at the stand scale. The nutrient fluxes estimated for February 2001 showed that for all ions, more than 50% of the ecosystem input was through fog deposition. These results demonstrate the importance of epiphytic bryophytes and fog deposition in nutrient cycling of this subtropical montane forest ecosystem. The incorporation of fog study in the long-term ecosystem research projects is necessary in this area.  相似文献   

11.
Concentration differences between small (r < 8.5 m) and large droplets(r > 8.5 m) were observed for formic acid, acetic acid and formaldehyde in fog droplets collected in California's Central Valley. The concentration ratios (large/small droplets) of these compounds were investigated by a stepwise model approach. Assuming thermodynamic equilibrium (KH eff) results in an overestimate of the concentration ratios. Considering the time dependence of gas phase diffusion and interfacial mass transport, it appears that the lifetime of fog droplets might be sufficiently long to enable phase equilibrium for formaldehyde and acetic acid, but not for formic acid (at pH 7). Oxidation by the OH radical has no effect on formaldehyde concentrations but reduces formic acid concentrations uniformly in all drop size classes. The corresponding reaction for acetic acid is less efficient so that only in large droplets, where replenishment is slowed because the uptake rate of acid from the gas phase is slower, is the acid concentration reduced leading to a smaller concentration ratio. Formaldehyde concentrations in fog can be higher than predicted by Henry's Law due to the formation of hydroxymethanesulfonate. Its formation is dependent on the sulfur(IV) concentration. At high pH values the uptake rate for sulfur(IV) is drop-size dependent. However, the observed concentration ratios for formaldehyde cannot be fully explained by the adduct formation. Finally, it is estimated that mixing effects, i.e., the combination of individual droplets into a bulk sample, have a minor influence (<15%) on the measured heterogeneities.  相似文献   

12.
Chemical characterization was performed on cloud and rainwater samples collected as part of the Rain In Cumulus over the Ocean Experiment (RICO). This experiment took place at a mountaintop site (East Peak) in Puerto Rico from December 2004 to March 2007 in order to determine water-soluble organic and nitrogen fractions in a marine background environment. For cloud water, similar average concentrations of 1.0 (±0.3) mg/L were found for total organic carbon (TOC) and total nitrogen (TN) and an average concentration of 0.8 (±0.2) mg/L was found for dissolved organic carbon (DOC). In rainwater, these concentrations were lower, ranging from 0.3 to 0.5 (±0.1) mg/L. Changes in the concentrations of these species were observed in periods under the influence of anthropogenic, African dust, and volcanic ash air masses. In these periods the concentrations of TOC, DOC, and TN were 2 to 4 times higher than in periods under the influence of trade winds. The insoluble organic material arriving during African dust events showed total carbon (TC) concentrations on averaging 1.5 mg/L for cloud water. The TC was composed mainly of organic carbon with polar compounds from low to high molecular weight (MW). The polar compounds with high MW were probably associated with pollution (e.g., fossil fuel combustion) from other regions. Crustal species (Al and Fe) dominated particles associated with dust episodes, confirming the soil origin. Our results suggested that a fraction (40–80%) of TOC and (<100%) of TN in Puerto Rican cloud/rainwater could be originated from long-range transport of dust, ash and/or pollution.  相似文献   

13.
This study aims at evaluating the variability of the optical properties of chromophoric dissolved organic matter (CDOM) of rainwater during the cold season, specifically between Autumn and Winter periods. The spectroscopic characteristics of rainwater samples collected at a town (Aveiro) in western Portugal were assessed by UV-Vis absorbance and three-dimensional excitation-emission matrix (EEM) fluorescence spectroscopies. Rainwater samples showed similar characteristics to those of natural humic substances when analysed by UV-Vis absorbance spectroscopy, but a significant difference was observed in the volume weight average (VWA) of absorbances between Autumn and Winter. In general, the EEM fluorescence spectra of the Autumn and Winter samples disclosed the presence of six fluorophores with different VWA specific fluorescence intensities: three humic-like (λ excitation/λ emission ≈ 230/415 nm; 290/415 nm; and 340/415 nm) and three protein-like (λ excitation/λ emission ≈ 230/350 nm; 280/340 nm; and 225/300 nm), but one of the humic-like peaks (≈340/415 nm) does not always appear in the EEM fluorescence spectra of the Winter samples. During the cold season, chromophoric compounds are important constituents of rainwater dissolved organic matter and the presence of these highly absorbing and fluorescing compounds may exert a determining effect in atmospheric absorption of solar radiation.  相似文献   

14.
Cloud/fog water samples were collected at Daekwanreung (840 m msl), a ridge site, in South Korea, from March 2002 to September 2003, by using a Caltech type, self fabricated active strand cloud water collector. The pH, electrical conductivity and major ion concentrations were analyzed. The cloud water pH ranged from 3.6 to 6.8 with an average of 5.2, which was close to the atmospheric neutral point. However, the pH calculated from average concentrations of H+ was 4.7, indicating the cloud/fog water was weakly acidified. SO4 2−, NO3 − and NH4 + are predominant ions of which average concentrations were 203.1, 128.1, and 211.7 μeq⋅L−1, respectively. Samples were categorized into four groups by applying 48-hour back trajectory analysis, using the HYbrid Single-Particle Largrangian Integrated Trajectory (HYSPLIT) model. Chemical compositions for the four cases significantly differed from each other. For air masses transported from the East Sea (group E), sea salt concentrations, including Na+, Cl− Mg2+, were relatively high. Principal acidifying pollutants, such as NO3 − and nss-SO4 2−, significantly increased in the case of air masses transported from the Northeast Asian continent through North Korea (group N) and air masses from the Seoul metropolitan area (group W). However, the mean pH of group N was the highest while the mean pH of group W was the lowest. This suggests that most NO3 − and nss-SO4 2− in cloud/fog water was neutralized by ammonia and calcium compounds under the influence of air masses transported from Northeast Asia. N/S ratio for the group W was significantly higher than those for the other three groups, suggesting nitrogen species transported from the Seoul metropolitan area contributed to acidification of cloud/fog water at Daekwanreung. Principle Component analysis (PCA) was applied to the cloud/fog water data for presenting characteristics in the four different categories.  相似文献   

15.
Organic compounds in the atmosphere can influence the activation, growth and lifetimes of haze, fog and cloud droplets by changing the condensation and evaporation rates of liquid water by these aqueous aerosol particles. Depending on the nature and properties of the organic compounds, the change can be to enhance or reduce these rates. In this paper we used a tandem differential mobility analyzer (TDMA) to examine the effect of tetracosane, octanoic acid, and lauric acid on the hygroscopic properties of NaCl aerosol particles at relative humidities (RH) between 30 and 95%. These organic compounds have been identified in ambient aerosol particle samples. A slight lowering of the deliquescence relative humidity (DRH) and suppression of hygroscopic growth for the NaCl-organic compound mixtures were observed when compared to pure NaCl particles. The growth of pure NaCl particles was 2.25 in diameter at 85% RH while the growth of the mixed particles was 1.3 to 1.7 in particle diameter at 85% RH with organic mass fraction of 30–50%. This shows that these organic compounds have to be present in rather large mass fractions to effect the hygroscopic behavior to a similar degree observed for ambient aerosol during field measurements. Despite the mixing of the organic material with NaCl, hysteresis was observed for decreasing RH histories, suggesting the formation of metastable droplets. These laboratory results are strikingly similar to ambient field results. For example, if the total organic mass fraction of the particles is between 0.30 and 0.50, the particle growth at 85% RH is about a factor of 1.4 for the laboratory and field measurements. Such reduction in growth compared to the pure inorganic salt is in contradiction to speculations concerning significant effects by organic compounds on cloud condensation nuclei and thus formation on clouds.  相似文献   

16.
The abundance and optical characteristics of dissolved organic matter (DOM) were determined in 120 rain samples collected in Wilmington, North Carolina, USA, between February 21, 2002 and August 11, 2003. All rainwater samples contained chromophoric dissolved organic matter (CDOM) as well as fluorescent compounds. The absorbance spectra of CDOM in the samples decreased exponentially with wavelength with little or no measurable absorbance past 550 nm. Fluorescence excitation emission spectra (EEMS) of the precipitation revealed the presence of four major peaks indicating both terrestrial and marine influences. There was a strong positive correlation between total integrated fluorescence and the absorbance coefficient at 300 nm in rainwater samples, suggesting that these optical properties are directly interrelated and that the compounds responsible for absorbance may be the same as those responsible for fluorescence. Air-mass back-trajectory analysis indicated elevated CDOM levels in continentally influenced rainwater relative to marine dominated events implying that anthropogenic and/or terrestrial sources are important contributors to CDOM levels in precipitation. The presence of highly absorbing and fluorescing CDOM in rainwater has significant ramifications in atmospheric chemistry and may play a previously unrecognized role in the wavelength dependent spectral attenuation of solar radiation by atmospheric waters.  相似文献   

17.
The chemical composition of fogwater has been studied in the city of Strasbourg (France) from 1990 to 1999. During these years, fogwater samples have been collected and analysed for major ions and trace metals. This paper reports on the analysis of the collected dataset. The analysis revealed a significant decrease in acidity of approximately one pH unit over the course of the study. This decrease in acidity appears to be linked to a decrease in SO2(g) and the resulting SO42−. Trace metal concentrations have also strongly decreased over the 10-year period. Pb concentrations, following the elimination of leaded gasoline, decreased by more than one order of magnitude.  相似文献   

18.
庐山2016年冬季三级分档雾水化学特征   总被引：1，自引：0，他引：1  
探究不同尺度雾滴化学特征是深化雾微物理化学研究的重要内容。2016年12月—2017年1月在庐山开展雾综合观测实验,利用主动式三级分档雾水采集器（CASCC 3_stage）收集到3次雾过程73个分档雾水样本,雾滴分档粒径:4—16 μm（3级）,16—22 μm（2级）和≥22 μm（1级）。定量得到了分档雾水的pH、电导率（EC）及9种水溶性无机离子（Na+、NH4+、K+、Mg2+、Ca2+、Cl-、NO2-、NO3-、SO42-）浓度（μeq/L）。结果表明,庐山冬季雾水酸化严重,pH为3.96—5.82,pH < 5.6的样品占98.6%且直径4—16 μm小雾滴的强酸性（pH < 4.5）样品最多,占比达54.2%,小雾滴酸性和电导率更强;NH4+、Ca2+、NO3-、SO42-是雾水的主要离子组分,[NH4++Ca2++NO3-+SO42-]分别在三级分档雾水中占总离子浓度（TIC）的83.8%、88.0%和88.7%;综合3次雾过程,总离子浓度、NH4+、K+、NO3-、SO42-在4—16 μm小雾滴存在富集,表现出尺度依赖特征;86%雾水样品[SO42-]/[NO3-]介于0.5—3.0,属于硫酸和硝酸混合型酸化,雾水酸化主要原因是碱性缓冲物质与酸性组分不平衡以及可能存在有机酸贡献;同一观测点不同雾过程化学特征存在个例差异,第二次雾过程（12月25日14时—26日21时）（北京时）,总离子浓度、NH4+、Ca2+、NO3-、SO42-在16—22 μm尺度雾滴存在富集,这可能是雾区气溶胶浓度较低、降温、采样间隔和污染气体及气溶胶输送共同作用的结果。后向轨迹聚类和潜在源（PSCF）分析表明,观测期间影响庐山的气团均来自西部,来自湖南北部的局地气团占总轨迹数的68.99%,最为重要;PM2.5、SO2、NO2具有相似潜在源区空间分布,主要位于湖北、湖南、安徽西南部和江西北部等邻近省份地区,以近距离输送为主。   相似文献   

19.
Iron occurs in rain as particulateand dissolved Fe and includes both Fe(II) and Fe(III)species. Model calculations and correlation analysisindicate Fe(II)(aq) occurs almost exclusively as thefree ion whereas Fe(III)(aq) occurs as both ironoxalate and Fe(OH)2 +(aq) with largevariations over the pH range from 4.0 to 5.0. Complexation with humic-like compounds may also beimportant for Fe(III)(aq); however, the concentrationand structural characteristics of these compounds haveyet to be determined. 112 rain samples were collectedfor iron analysis in Wilmington, North Carolina,between 1 July 1997, and 30 June 1999. Total iron,particulate iron and Fe(III)(aq) were higher inconcentration in summer and spring rain relative towinter and autumn rain. Fe(II)(aq) concentrations, incontrast, did not vary seasonally. Particulate iron,which was approximately half the total rainwater iron,was highest between noon and 6 p.m. (EST), probably dueto more intense regional convection including land-seabreezes during that time. The ratio ofFe(II)(aq)/Fe(III)(aq) was also highest in rainreceived between noon and 6 p.m., which most likelyreflects photochemical reduction of Fe(III)(aq)complexes to form Fe(II)(aq). A conceptual modeldepicting the interplay between iron species, lightintensity and organic ligands in rainwater ispresented.  相似文献   

20.
Wet deposition due to radiation fog is examined in this paper. The area where the reported measurements were performed, the Po Valley, northern Italy, is characterized by both a high fog occurrence during the fall-winter months and fog water solutions of high ionic concentration and acidity.Estimated wet deposition for NH 4 + , NO inf3 sup- and SO inf4 sup2- ions due to fog droplet settling to the ground accounts for 13.2, 12.1 and 5.3 percent with respect to bulk precipitations over the same period: January–March and October–December (fog season).Fog deposition rates show that this process can be an important pathway of trace gases and particles loss from the air. First indicative results of fog removal efficiency with respect to air particulate matter are presented.Dry deposition parameters should be taken into account in evaluating the potential effect of fog droplet deposition on vegetation.  相似文献   

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