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1.
In this study, variations of the chemical composition of precipitation in Nanjing, China, over a 12-year period (1992–2003) are presented. The average annual concentration of pH value was 5.15, ranging from 4.93 to 5.36, and there was no significant trend in the acidity of precipitation. SO42−, Cl− and NO3− were the main anions, while Ca2+, NH4+ and Mg2+ were the main cations. The concentrations of these main ions were very high compared to those reported in many other areas around the world. Most of the ions came from anthropogenic and crustal sources. High correlations were found among dust-derived cations Ca2+, Mg2+and K+, between Cl− and SO42−, between Cl− and NH4+ and between acidic anions and dust-derived cations, such as SO42− and Ca2+, SO42− and K+, Cl− and Ca2+, Cl− and K+, F− and Mg2+ and F− and K+. A significant decreasing trend was observed in concentration of SO42− because of the abatement strategies for SO2 emissions and energy policy change, while a significant increasing trend was found in the contribution of NO3− to acidification due to the rapidly growing number of motor vehicles. A significant decreasing trend was found in dust-derived cation Ca2+ due to more stringent controls of industrial dust emissions and rapid urbanization reducing the amount of open land, while the contribution of NH4+ to neutralization increased relatively.  相似文献   

2.
This study describes the chemical composition of dry deposition collected at a highway traffic site in central Taiwan during daytime and nighttime periods by using a dry deposition plate (DDP) and water surface sampler (WSS). In addition, the characterization for mass and water-soluble species of total suspended particulate (TSP), both PM2.5 and PM10, was studied at the study site from August 22 to November 30, 2006. Dry deposition fluxes of ambient air particulates and inorganic species (Na+, NH4+, K+, Mg2+, Ca2+, Cl−, NO3− and SO42−) were analyzed by Ion Chromatography (DIONEX-100).Results of the particulate dry deposition fluxes and mass concentrations are higher in the water surface sampler with respect to the dry deposition plate used in this study. Statistical results also showed the average dry deposition flux of the ionic species (Na+, NH4+, K+, Cl−, NO3− and SO42−) obtained by the DDP and WSS displayed significant differences. Also, the average concentrations of Mg2+ and, Ca2+ were statistically the same at this study site.  相似文献   

3.
The apportionment of atmospheric aerosols undertaken in Northern France during two sampling campaigns allowed to determine the influence of the atmospheric contribution of a heavy industrialized urban center on the particulate matter composition at a nearby rural site. The concentrations of major components and trace elements sampled by bulk filtration have been determined on June–July 2000 and January–February 2001, and the comparison of these two campaigns shows very well the importance of wind directions. The sources of 10 trace elements (Al, Ba, Cu, Fe, K, Mn, Pb, Sr, Ti and Zn) and 7 major components (Cl−, NO3−, SO42−, NH4+, Na, Mg and Ca) are better identified by studying their elemental contribution at each sampling site according to wind sectors. This kind of study shows that the concentrations recorded at the urban sampling site are always higher than those observed at the rural site as well during the summer campaign (about + 35%) as during the winter campaign (+ 90%), because of the predominance of the W–NW wind sector, corresponding to the influence of the urban and industrialized areas.  相似文献   

4.
《Atmospheric Research》2005,73(1-2):1-22
We compare the characteristics of dew at nearly the same latitude (42–45°N) for the Mediterranean island of Corsica (Ajaccio, France) and two continental locations (Bordeaux, France, Atlantic coastal area; Grenoble, France, alpine valley). Dew amount was measured on a horizontal reference plate made of polymethylmethacrylate (PMMA) and placed at 1 m above the ground. Data are correlated with plate and air temperature, air relative humidity, wind speed and cloud cover during the period from 14-08-1999 to 15-01-2003.General features as well as particularities of the sampling sites are discussed. The average daily dew yield is higher for the island station at Ajaccio (0.070 mm) than the Bordeaux coastal area (0.046 mm) or the Grenoble valley (0.036 mm). However, the accumulated dew yield was highest for the coastal station (9.8 mm/year) as compared to the island (8.4 mm/year), and much larger than in the alpine valley (4 mm/year). The difference between cumulated and average dew yield stems from the greater number of dew days in the coastal area (58%) versus 33% for the island and 30% in the valley. The higher wind speeds at the island station (average wind during dew is 2 m/s) and lower relative humidity explain the smaller number of dew days. The dew rate seasonal variation is negligible in Bordeaux and exhibits during summer a maximum in Ajaccio and a minimum in Grenoble.A computer model that includes simple meteorological data (air temperature and relative humidity, wind speed, cloud cover) is used to determine the thermal balance and fit to dew mass evolution. Two parameters that account for heat and mass exchange can be adjusted. It was found that, within the uncertainties, these two numbers are the same for the two continental sites, thus allowing dew formation on plates to be evaluated from only simple meteorological measurements. Somewhat larger values are found for the island, due to limitations in the model, which are discussed.  相似文献   

5.
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   

6.
A comprehensive study on the chemical compositions of wet precipitation was carried out from January 2004 to December 2004 in Jinhua, southeastern China's Zhejiang Province. All samples were analyzed for pH, electrical conductivity and major ions (F−, Cl−, NO3−, SO42−, K+, Na+, Ca2+, Mg2+ and NH4+). The rainwater was typically acidic with a volume-weighted mean pH of 4.54, which ranged from 3.64 to 6.76. SO42− and NO3− were the main anions, while NH4+ and Ca2+ were the main cations. The concentrations of these major ions were generally higher compared to those reported in other parts of the world, but much lower than those in northern China.Wet deposition fluxes of major ions showed pronounced seasonal variations with maximum in spring and minimum in autumn. Significant correlations were found in soil-derived species among Ca2+, Mg2+ and K+ and sea-salt species between Na+ and Cl−. Other relatively good correlations were also observed between Ca2+ and SO42-, Mg2+ and SO42-, Mg2+ and NO3−, Mg2+ and Cl−. Principal component analysis was also performed on individual precipitation to find possible sources of the major ionic species. Varimax rotated four components accounting for 85.9% of the total variance, and were interpreted as acid and alkaline pollutants, sea spray and mixed source, soil and acid/neutralization. Calculation of enrichment factors for rainwater components relative to soil and seawater indicated that Ca2+ and K+ mainly originated from the terrestrial source, and SO42- and NO3− were mostly attributed for the anthropogenic activities in the study area. In general, the results suggested that precipitation chemistry is strongly influenced by anthropogenic sources rather than natural and marine sources. The pollutants in rainwater were mainly derived from long distance transport, local industry and traffic sources.  相似文献   

7.
In this paper, the basic composition of fog and low cloud water are presented, resulting from the analyses of water samples from 111 fog/cloud events. The samples were collected at five sites located in various regions of the Czech Republic. Two sampling sites are in mountainous regions and three sites represent various urban areas. The mountain stations are located in two regions of the Czech Republic with different industry types. At all the sites, active fog collectors were employed. In the water samples, the conductivity, acidity (pH), cations (H+, Na+, K+, NH4+, Mg2+, Ca2+) and anions (F−, Cl−, NO3−, SO42−) were determined.A mean pH value of about 4.5 was obtained at mountain sites whereas the measurements in urban areas showed mean pH values from 4.9 to 6.4. The mean conductivity values in the samples from the two mountain stations were 137 and 191.5 μS cm−1. The samples from urban sites showed mean values between 127.7 and 654.4 μS cm−1. The maximum concentration means for the three dominant pollutants (expressed by the ratio mountain sites/urban sites) are 32.9/99.6 mg l−1 for NO3−, 32.5/192.9 mg l−1 for SO42− and 18.5/52.7 mg l−1 for NH4+. As expected, we found higher ion concentrations in the northern part of the Czech Republic where larger numbers of lignite-burning power plants, chemical factories and opencast lignite mines are located. A decrease in ion concentrations was observed at higher altitude sites, probably reflecting at least in part higher liquid water contents at these locations.  相似文献   

8.
In the present study, the wet and dry depositions of particulate NO3−, SO42−, Cl− and NH4+ were measured using a wet/dry sampler as a surrogate surface. Gas phase compounds of nitrogen, sulfur and chloride (HNO3, NH3, SO2 and HCl) were measured by an annular denuder system (ADS) equipped with a back up filter for the collection of particles with diameter ≤ 5 μm. Ambient concentrations of NO, NO2 and SO2 were also taken into consideration. Sampling was conducted at an urban site in the center of the city of Thessaloniki, northern Greece. The presence of the aerosol species was examined by cold/warm period and the possible compounds in dry deposits were also considered. Dry deposition fluxes were found to be well correlated with ambient particle concentrations in order to be used for the calculation of particle deposition velocity. Average particulate deposition velocities calculated were 0.36, 0.20, 0.20 and 0.10 cm s− 1 for Cl−, NO3−, SO42− and NH4+, respectively. Total dry deposition fluxes (gas and particles) were estimated at 3.24 kg ha− 1 year− 1 for chloride (HCl + p-Cl), 9.97 kg ha− 1 year− 1 for nitrogen oxidized (NO + NO2 + HNO3 + p-NO3), 5.32 kg ha− 1 year− 1 for nitrogen reduced (NH3 + p-NH4) and 15.77 kg ha− 1 year− 1 for sulfur (SO2 + p-SO4). 70–90% total dry deposition was due to gaseous species deposition. The contribution of dry deposition to the total (wet + dry) was at the level of 60–70% for sulfur and nitrogen (oxidized and reduced), whereas dry chloride deposition contributed 35% to the total. The dry-to-wet deposition ratio of all the studied species was found to be significantly associated with the precipitation amount, with nitrogen species being better and higher correlated. Wet, dry and total depositions measured in Thessaloniki, were compared with other countries of Europe, US and Asia.  相似文献   

9.
The pH variation and chemical characteristics of rainwater were investigated from January 2006 to December 2006 at an urban site of Guangzhou, South China. The rainwater was typically acidic with a volume-weighted mean pH value of 4.49, which ranged from 3.52 to 6.28. The volume-weighted mean equivalent concentration of components followed the order: SO42− > Ca2+ > Cl− > NH4+ > Na+ > NO3− > K+ > Mg2+ > F−, indicating that SO42−, Cl− and NO3− were the main anions, while Ca2+ and NH4+, were the main cations. Ca2+ and NH4+ were major neutralization constituents of the precipitation. Furthermore, correlation analysis and principal component analysis method were performed to identify possible common sources of major ions. Sources of the major ions were assessed based on enrichment factor method.  相似文献   

10.
The formation of dew, deposition of frost and accumulation of snow mainly on the upper domes of a non-ventilated net radiometer seriously affect the measurement of available energy (net radiation). Net radiometers measure radiation, and energy balances and are widely used for estimation of evapotranspiration throughout the world. To study the effects of dew, frost, and snow on a non-ventilated net radiometer, a radiation station was set up which uses 2 CM21 Kipp & Zonen pyranometers (one inverted), 2 CG1 Kipp & Zonen pyrgeometers (one inverted), along with a Q7.1 net radiometer (Radiation & Energy Balance Systems, Inc.; REBS) in a semi-arid mountainous valley in Logan, Utah, U.S.A. The pyranometers and pyrgeometers were ventilated using 4 CV2 Kipp & Zonen ventilation systems. The net radiometer was not ventilated. The ventilation of pyranometers and pyrgeometers prevents dew and frost deposition and snow accumulation which otherwise would disturb measurements. All sensors were installed at about 3.0 m above the ground, which was covered with natural vegetation during the growing season (May–September). The incoming and outgoing solar or shortwave radiation, the incoming (atmospheric) and outgoing (terrestrial) longwave radiation, and the net radiation have been continuously measured by pyranometers, pyrgeometers and a net radiometer, respectively, since 1995. These parameters have been measured every 2 s and averaged into 20 min. To evaluate the effects of dew, frost, and snow, three days were chosen: 26 April 2004 with early morning dew, 6 January 2005 with an early morning frost, and the snowy day of 24 February 2005. Dew formation, frost deposition, and snow accumulation occurred mainly on the upper dome of the non-ventilated Q7.1 net radiometer on the related days, while the ventilated Kipp & Zonen system was free of dew, frost and snow. Net radiation measured by the non-ventilated net radiometer Rn,unvent. during dew and frost periods of the above-mentioned days was greater than ventilated ones Rn,vent. (− 0.2 MJ m− 2 vs. − 0.8 MJ m− 2 during almost 4 h on 26 April 2004, and − 0.2 MJ m− 2 vs. − 0.7 MJ m− 2 during almost 6.5 h on 6 January 2005). The reason for higher reading by the non-ventilated net radiometer during dew and frost periods was due to emission of additional longwave radiation from water and ice crystals formed mainly on the upper dome of the Q7.1 net radiometer. In contrast, during the snowy day of 24 February 2005, the Rn,unvent. was less than Rn,vent. (− 4.00 MJ m− 2 vs. 0.77 MJ m− 2, mainly from sunrise to sunset). The extremely low Rn,unvent. measured by the non-ventilated net radiometer on 24 February 2005 is due to blocking of the incoming solar radiation (mainly diffuse radiation) by the snow-covered upper dome.  相似文献   

11.
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   

12.
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   

13.
In the present study, the precipitation near Büyükçekmece Lake, which is one of the important drinking water sources of Istanbul city, was studied during October 2001–July 2002. Seventy-nine bulk precipitation samples were collected at two sampling stations near the Lake (41°2′35″N, 28°35′25″E and 41°5′30″N, 28°37′7″E). The study comprised the determination of H+, Cl−, NO3−, SO42−, NH4+, Na, K, Mg, Ca, Al, Ba, Fe, Cu and Mn concentrations in bulk deposition rain event samples. The average volume-weighted pH value was found to be 4.81, which points out that the rain is slightly acidic. High sulfate concentrations were observed together with high H+ ion values. Sulfur emissions were the major cause for the observed high hydrogen ion levels. On the basis of factor analysis and correlation matrix analysis, it has been found that in this region, acid neutralization is brought about by calcium rather than the ammonium ion. The varimax rotated factor analysis grouped the variables into four factors, which are crustal, marine and two anthropogenic sources.  相似文献   

14.
Columnar observations of liquid water and of radar echo intensity in cloud were carried out, using a microwave radiometer and a vertically pointing radar respectively, in Ny-Ålesund, Svalbard. Chemical concentrations were also measured in aerosols, gases and snowfalls. Clouds with a large proportion of liquid water moved over the site after snow clouds, with a much lower liquid water content, had been present for about 16 h. The mass concentrations of most chemical species in snowfalls were lower from the first set of clouds than the second. The NO3− and SO42− concentrations in gases and aerosols associated with the first set of clouds were higher than in the second set, but Cl− concentration was less for the first set than the second.  相似文献   

15.
Dew and rain water collection in the Dalmatian Coast, Croatia   总被引：1，自引：0，他引：1  
Passive dew harvesting and rainwater collection requires a very small financial investment but can exploit a free, clean (outside urban/industrial zones) and inexhaustible source of water. This study investigates the relative contributions of dew and rain water in the Mediterranean Dalmatian coast and islands of Croatia, with emphasis on the dry summer season. In addition, we evaluate the utility of transforming abandoned roof rain collectors (“impluviums”) to collect dew water too. Two sites were chosen, an exposed open site on the coast favourable to dew formation (Zadar) and a less favourable site in a cirque of mountains in Komiža (Vis Island). Between July 1, 2003 and October 31, 2006, dew was collected two or three times per day on a 1 m2 inclined (30°) test dew condenser, together with standard meteorological data (air temperature and relative humidity, cloud cover, windspeed and direction). Maximum yields were 0.41 mm in Zadar and 0.6 mm in Komiža. The mean yearly cumulative dew yields were found to be 20 mm (Zadar) and 9.3 mm (Komiža). Because of its physical setting, Komiža represents a poor location for dew collection. However, during the dry season (May to October), monthly cumulative dew water yield can represent up to 38% of water collected by rainfall. In both July 2003 and 2006, dew water represented about 120% of the monthly cumulative rain water. Refurbishing the abandoned impluviums to permit dew collection could then provide useful supplementary water, especially during the dry season. As an example, the 1300 m2 impluvium at Podšpilje near Komiža could provide, in addition to rain water, 14,000 L dew water per year.  相似文献   

16.
Inorganic ions and trace metals in total suspended particles were measured during the period 2006–2007 at four sites; three urban sites in the Mexico City Metropolitan Area (MCMA) and one nearby rural site in the state of Morelos. SO42−, NO3−, Cl− and NH4+ ions were analyzed by ion chromatography; Na+, K+, Ca2+ and Mg2+ by flame atomic absorption spectroscopy, and Al, Cd, Cr, Mn, Pb and V by an atomic absorption spectrometer with a graphite furnace attachment. The results indicated that SO42− was the most abundant ion. All trace elements except Mn and V showed statistically significant differences between sampling sites. Pearson's correlation applied to all data showed a high correlation among SO42−, NO3− and NH4+, indicating a common anthropogenic origin. In addition, the correlation observed between Ca2+ and Al indicated a crustal origin, as supported by the enrichment factors. Over the total sampling period, significant differences in particles and trace metals were found between sites and meteorological seasons. To gain a better insight into the origin of trace metals and major inorganic ions, a Principal Component Analysis was applied to the results for six trace metal and eight inorganic ions.  相似文献   

17.
Intensive measurements of gas and aerosol for 2 weeks were carried out at Qingdao (gas and aerosol in 2000, 2001 and 2002), Fenghuangshan (gas and aerosol in 2000 and 2001), and Dalian (aerosol in 2002) in the winter–spring period. High SO2 episodes were observed on 18 January 2000 at both Qingdao and Fenghuangshan. According to back trajectory calculations and analysis of gaseous species, high SO2 episodes were caused by local pollution and transport.Nitrate, sulfate and ammonium were the major species in PM2.5. Mass fractions of NO3−, nss-SO42− and NH4+ at Qingdao in 2002 were 10%, 12% and 5.5% for PM2.5, respectively, which were higher than that of nss-Ca2+ (1%). Chemical compositions observed at Dalian and Fenghuangshan were similar to those at Qingdao. The mass ratio of nss-SO42−/SO2 at Qingdao in winter was low (< 1.2), indicating that sulfate was probably produced by the slow oxidation of SO2 in the gas phase and/or was transported from outside of Qingdao in winter. The equivalent ratio of NH4+ to nss-SO42− was 1.39, suggesting that ammonium sulfate was one of the major chemical compositions in PM2.5. The NO3−/SO42− ratio at Qingdao was higher than that at remote places in East Asia. Gas and aerosol data obtained at Fenghuangshan were similar to data at Qingdao, suggesting that emissions from small cities may have a great influence on pollution in northern China.  相似文献   

18.
In this study bulk airborne aerosol composition measured by the PILS-IC (integration time of 3 min 24 s) during TRACE-P P3B Flight 10 are used to investigate the ionic chemical composition and mixing state of biomass burning particles. A biomass burning plume, roughly 3–4 days old, moderately influenced by urban pollution aerosols recorded in the Philippine Sea is investigated. Focusing on the fine particle NO3−, SO42−, K+, NH4+, and water-soluble organics, the observed correlations and nearly 1-to-1 molar ratios between K+ and NO3− and between NH4+ and (SO42−+ inferred Organics) suggest the presence of fine-mode KNO3, (NH4)2SO4, and NH4(Organics) aerosols. Under the assumption that these ion pairs existed, and because KNO3 is thermodynamically less favored than K2SO4 in a mixture of NO3−, SO42−, K+, NH4+, and Organic anions, the measurements suggest that aerosols could be composed of biomass burning particles (KNO3) mixed to a large degree externally with the (NH4)2SO4 aerosols. A “closed-mode” thermodynamic aerosol simulation predicts that a degree of external mixing (by SO42− mass) of 60 to 100% is necessary to achieve the observed ionic associations in terms of the existence of KNO3. However, the degree of external mixing is most likely larger than 90%, based on both the presence of KNO3 and the amounts of NH4NO3. Calculations are also shown that the aerosol mixing state significantly impacts particle growth by water condensation/evaporation. In the case of P3B Flight #10, the internal mixture is generally more hygroscopic than the external mixture. This method for estimating particle mixing state from bulk aerosol data is less definitive than single particle analysis, but because the data are quantitative, it may provide a complementary method to single particle chemical analysis.  相似文献   

19.
The results presented are the first complete analysis of inorganic soluble ions in a tropical savannah region. Atmospheric particles were collected in six rural Venezuelan savannah sites. Concentrations and size distribution of NO3 –, SO4 2-, CI–, PO4 3-, NH4 +, Na+, K+, Ca2+ and Mg2+ were determined in samples collected with Hi Vol samplers equipped with five-stage cascade impactors. Concentrations were higher in the dry season, with a maximum during the burning periods. Using Na+ as a reference, the results show a deficit of Cl– and, with the exception of Mg2+, an enrichment of all other ions with respect to marine aerosols. Significant variations were observed in particle-size distribution between different periods. Various pairs of ions present similar size distributions: SO4 2- and NH4 +; Cl– and Na+; PO4 3- and K+; Ca2+, Mg2+ and NO3 –; indicating that the ions were produced by the same source and/or were involved in similar atmospheric processes. Possible primary sources, the gas-to-particle atmospheric process, environmental implication of long-range transport of nutrients during dry seasons, etc., are discussed.  相似文献   

20.
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   

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