Study of a high SO2 event observed over an urban site in western India

Continuous measurements of SO₂, NO_x and O₃ along with sampling based measurements of CO, CH₄, NMHCs and CO₂ were carried out during May, 2010 at Ahmedabad. The diurnal variations of SO₂ in ambient air exhibited elevated values during the night and lower levels during the sunlit hours. The mean concentration of SO₂ during the study period was 0.95 ± 0.88 ppbv. However, the ambient SO₂ exceeded 17 ppbv in the night of 20 May, 2010. On the same day, tropospheric columnar SO₂ from OMI showed almost 350% increase corroborating the surface observations over an extended height regime. This was also the highest columnar value of SO₂ during the summer of 2010. Columnar loadings were also found to be high for formaldehyde, precipitable water vapor and aerosol optical depth on 20 May. Elevated concentrations were also recorded for other trace gases like NO₂ and O₃. Analysis of related data of trace gases indicated characteristics of fresh emissions with dominant contributions from mobile sources during the study period. However, SO₂/NO₂ ratio of 0.36 during the event period on 20th May connotes non-local influences. Analyses of meteorological parameters suggest combined impacts of transport and inversion causing higher levels of SO₂ and other pollutants during 20?C21 May. Episodes of such enhancements may perturb chemical and radiative balance of the atmosphere.     

人为大气污染物对一次冬季浓雾形成发展的影响研究

基于WRF/Chem模式和雾的观测资料,开展了包含和不包含人为污染排放源两种大气背景条件下的数值模拟对比试验,在此基础上探讨了人为污染物对2009年12月1日发生在我国华北和华东地区的一次浓雾天气过程的影响机理.结果表明,在考虑污染排放源时,模式模拟的雾的空间分布和强度变化与卫星、能见度仪和微波辐射计的观测更为接近.污...     

Distributions of ozone and related trace gases at an urban site in western India

Continuous in-situ measurements of surface ozone (O₃), carbon monoxide (CO) and oxides of nitrogen (NOx) were conducted at Udaipur city in India during April 2010 to March 2011. We have analyzed the data to investigate both diurnal and seasonal variations in the mixing ratios of trace gases. The diurnal distribution of O₃ showed highest values in the afternoon hours and lower values from evening till early morning. The mixing ratios of CO and NOx showed a sharp peak in the morning hours but lowest in the afternoon hours. The daily mean data of O₃, CO and NOx varied in the ranges of 5–51 ppbv, 145–795 ppbv and 3–25 ppbv, respectively. The mixing ratios of O₃ were highest of 28 ppbv and lowest 19 ppbv during the pre-monsoon and monsoon seasons, respectively. While the mixing ratios of both CO and NOx showed highest and lowest values during the winter and monsoon seasons, respectively. The diurnal pattern of O₃ is mainly controlled by the variations in photochemistry and planetary boundary layer (PBL) depth. On the other hand, the seasonality of O₃, CO and NOx were governed by the long-range transport associated mainly with the summer and winter monsoon circulations over the Indian subcontinent. The back trajectory data indicate that the seasonal variations in trace gases were caused mainly by the shift in long-range transport pattern. In monsoon season, flow of marine air and negligible presence of biomass burning in India resulted in lowest O₃, CO and NOx values. The mixing ratios of CO and NOx show tight correlations during winter and pre-monsoon seasons, while poor correlation in the monsoon season. The emission ratio of ?CO/?NOx showed large seasonal variability but values were lower than those measured over the Indo Gangetic Plains (IGP). The mixing ratios of CO and NOx decreased with the increase in wind speed, while O₃ tended to increase with the wind speed. Effects of other meteorological parameters in the distributions of trace gases were also noticed.     

Urban air pollution: process identification, impact analysis and evaluation of forecast potential

The daily variations in the atmospheric pollutants like suspended particulate matter (SPM), respirable suspended particulate matter (RSPM), sulphur dioxide (SO₂) and nitrogen dioxide (NO₂) depend on both local meteorological processes and various natural as well as anthropogenic sources and sinks. It was shown in an earlier work (Goswami and Baruah in Mon Wea Rev 136(9):3597?C3607, 2008) that the daily variations in SPM over a location could be simulated quite well by considering daily meteorological fields from NCEP Reanalysis in combination with a model for natural and anthropogenic sources over Delhi. In the present work, we extend the scope of the model to include three other pollutants: RSPM, SO₂ and NO₂. While the basic conservation equations and the meteorological fields are common to all the three (and SPM) pollutants, the sources and sinks for each is modeled in a species-specific manner to obtain maximum skill. As we do not consider active chemistry, the present model provides the minimal dynamics of pollution over an urban location in terms of annual load; the model error is about 10% on the average, with no significant bias for any of the species.     

Investigating the Changes in Air Pollutant Emissions over the Beijing-Tianjin-Hebei Region in February from 2014 to 2019 through an Inverse Emission Method

In recent years, China has implemented several measures to improve air quality. The Beijing-Tianjin-Hebei(BTH)region is one area that has suffered from the most serious air pollution in China and has undergone huge changes in air quality in the past few years. How to scientifically assess these change processes remain the key issue in further improving the air quality over this region in the future. To evaluate the changes in major air pollutant emissions over this region, this paper employs ens...     

Tropospheric chemical composition measurements in Brazil during the dry season

Field measurement programs in Brazil during the dry seasons in August and September 1979 and 1980 have demonstrated the large importance of the continental tropics in global air chemistry. Many important trace gases are produced in large amounts over the continents. During the dry season, much biomass burning takes place, especially in the cerrado regions, leading to a substantial emission of air pollutants, such as CO, NO _x , N₂O, CH₄ and other hydrocarbons. Ozone concentrations are enhanced due to photochemical reactions. The large biogenic organic emissions from tropical forests play an important role in the photochemistry of the atmosphere and explain why CO is present in such high concentrations in the boundary layer of the tropical forest. Carbon monoxide production may represent more than 3% of the net primary productivity of the tropical forests. Ozone concentrations in the boundary layer of the tropical forests indicate strong removal processes. Due to atmospheric supply of NO _x by lightning, there is probably a large production of O₃ in the free troposphere over the Amazon tropical forests. This is transported to the marine-free troposphere and to the forest boundary layer.     

Trace gases and PM2.5-bound metal abundance over a tropical urban environment,South India

Pre and Post-Monsoon levels of ambient SO₂, NO₂, PM_2.5 and the trace metals Fe, Cu, etc. were measured at industrial and residential regions of the Kochi urban area in South India for a period of two years. The mean PM_2.5, SO₂ and NO₂ concentrations across all sites were 38.98?±?1.38 µg/m³, 2.78?±?0.85 µg/m³ and 11.90?±?4.68 µg/m³ respectively, which is lower than many other Indian cities. There was little difference in any on the measured species between the seasons. A few sites exceeded the NAAQS (define acronym and state standard) and most of the sites exceeded WHO (define acronym and state standard) standard for PM_2.5. The average trace metal concentrations (ng/m³) were found to be Fe (32.58)?>?Zn (31.93)?>?Ni (10.13)?>?Cr (5.48)?>?Pb (5.37)?>?Cu (3.24). The maximum concentration of trace metals except Pb were reported in industrial areas. The enrichment factor, of metals relative to crustal material, indicated anthropogenic dominance over natural sources for the trace metal concentration in Kochi’s atmosphere. This work demonstrates the importance of air quality monitoring in this area.

     

Abatement of Greenhouse Gases: Does Location Matter?

Today's climate policy is based on the assumption that the location of emissions reductions has no impact on the overall climate effect. However, this may not be the case since reductions of greenhouse gases generally will lead to changes in emissions of short-lived gases and aerosols. Abatement measures may be primarily targeted at reducing CO₂, but may also simultaneously reduce emissions of NO_x, CO, CH₄ and SO₂ and aerosols. Emissions of these species may cause significant additional radiative forcing. We have used a global 3-D chemical transport model and a radiative transfer model to study the impact on climate in terms of radiative forcing for a realistic change in location of the emissions from large-scale sources. Based on an assumed 10% reduction in CO₂ emissions, reductions in the emissions of other species have been estimated. Climate impact for the SRES A1B scenario is compared to two reduction cases, with the main focus on a case with emission reductions between 2010 and 2030, but also a case with sustained emission reductions. The emission reductions are applied to four different regions (Europe, China, South Asia, and South America). In terms of integrated radiative forcing (over 100 yr), the total effect (including only the direct effect of aerosols) is always smaller than for CO₂ alone. Large variations between the regions are found (53–86% of the CO₂ effect). Inclusion of the indirect effects of sulphate aerosols reduces the net effect of measures towards zero. The global temperature responses, calculated with a simple energy balance model, show an initial additional warming of different magnitude between the regions followed by a more uniform reduction in the warming later. A major part of the regional differences can be attributed to differences related to aerosols, while ozone and changes in methane lifetime make relatively small contributions. Emission reductions in a different sector (e.g. transportation instead of large-scale sources) might change this conclusion since the NO_x to SO₂ ratio in the emissions is significantly higher for transportation than for large-scale sources. The total climate effect of abatement measures thus depends on (i) which gases and aerosols are affected by the measure, (ii) the lifetime of the measure implemented, (iii) time horizon over which the effects are considered, and (iv) the chemical, physical and meteorological conditions in the region. There are important policy implications of the results. Equal effects of a measure cannot be assumed if the measure is implemented in a different region and if several gases are affected. Thus, the design of emission reduction measures should be considered thoroughly before implementation.     

Evolution of anthropogenic and biomass burning emissions of air pollutants at global and regional scales during the 1980�C2010 period

Several different inventories of global and regional anthropogenic and biomass burning emissions are assessed for the 1980?C2010 period. The species considered in this study are carbon monoxide, nitrogen oxides, sulfur dioxide and black carbon. The inventories considered include the ACCMIP historical emissions developed in support of the simulations for the IPCC AR5 assessment. Emissions for 2005 and 2010 from the Representative Concentration Pathways (RCPs) are also included. Large discrepancies between the global and regional emissions are identified, which shows that there is still no consensus on the best estimates for surface emissions of atmospheric compounds. At the global scale, anthropogenic emissions of CO, NO_x and SO₂ show the best agreement for most years, although agreement does not necessarily mean that uncertainty is low. The agreement is low for BC emissions, particularly in the period prior to 2000. The best consensus is for NO_x emissions for all periods and all regions, except for China, where emissions in 1980 and 1990 need to be better defined. Emissions of CO need better quantification in the USA and India for all periods; in Central Europe, the evolution of emissions during the past two decades needs to be better determined. The agreement between the different SO₂ emissions datasets is rather good for the USA, but better quantification is needed elsewhere, particularly for Central Europe, India and China. The comparisons performed in this study show that the use of RCP8.5 for the extension of the ACCMIP inventory beyond 2000 is reasonable, until more global or regional estimates become available. Concerning biomass burning emissions, most inventories agree within 50?C80%, depending on the year and season. The large differences between biomass burning inventories are due to differences in the estimates of burned areas from the different available products, as well as in the amount of biomass burned.     

Simultaneous measurements of ozone and its precursors on a diurnal scale at a semi urban site in India

Simultaneous observations of surface ozone (O₃) with its precursors namely, carbon monoxide (CO) and oxides of nitrogen (NO_x) have been taken on diurnal scale from a tropical semi-urban site, Pune (18.54°N, 73.81°E) in India. We present the data for one year (2003–2004) period to study the salient features of these trace gases. The peak in amplitude of ozone is found during the noontime whereas in CO and NO_X it is observed in the morning hours between 0800 and 0900 H. The concentration of these pollutants drop down considerably during southwest monsoon months and the diurnal pattern also become very weak. The diurnal trends of these gases are found to be different for different seasons, which are specific to the receptor site. Model simulations using 3-D chemical-transport model with regional emission inventories and observed winds have also been carried out. The comparison of model results with observations, on seasonal basis yielded a reasonable qualitative agreement. The relative role of local emissions and long range transport in the diurnal pattern for different seasons has been outlined, which reveals that the ozone is highly influenced by regional/long range transport in this region. The effect of precursor amounts in the morning on afternoon ozone peak levels has been investigated using the lag correlation study, which reveals that a time lag of 5–7 h is required for most of these precursor gases to photo-chemically produce ozone to its maximum potential. Results are discussed in the light of available topographic and meteorological conditions.     

Synoptic weather conditions and aerosol episodes over Indo-Gangetic Plains,India

The present study focuses on identifying the main atmospheric circulation characteristics associated with aerosol episodes (AEs) over Kanpur, India during the period 2001–2010. In this respect, mean sea level pressure (MSLP) and geopotential height of 700 hPa (Z700) data obtained from the NCEP/NCAR Reanalysis Project were used along with daily Terra-MODIS AOD₅₅₀ data. The analysis identifies 277 AEs [AOD₅₀₀ >  \( \overline{AOD} \) ₅₀₀ + 1STDEV (standard deviation)] over Kanpur corresponding to 13.2 % of the available AERONET dataset, which are seasonally distributed as 12.5, 9.1, 14.7 and 18.6 % for winter (Dec–Feb), pre-monsoon (Mar–May), monsoon (Jun–Sep) and post-monsoon (Oct–Nov), respectively. The post-monsoon and winter AEs are mostly related to anthropogenic emissions, in contrast to pre-monsoon and monsoon episodes when a significant component of dust is found. The multivariate statistical methods Factor and Cluster Analysis are applied on the dataset of the AEs days’ Z700 patterns over south Asia, to group them into discrete clusters. Six clusters are identified and for each of them the composite means for MSLP and Z700 as well as their anomalies from the mean 1981–2010 climatology are studied. Furthermore, the spatial distribution of Terra-MODIS AOD₅₅₀ over Indian sub-continent is examined to identify aerosol hot-spot areas for each cluster, while the SPRINTARS model simulations reveal incapability in reproducing the large anthropogenic AOD, suggesting need of further improvement in model emission inventories. This work is the first performed over India aiming to analyze and group the atmospheric circulation patterns associated with AEs over Indo-Gangetic Plains and to explore the influence of meteorology on the accumulation of aerosols.     

不同人为源排放清单对大气污染物浓度数值模拟的影响:以浙江省为例

应用大气化学模式WRF-Chem(Weather Research and Forecast-Chemistry),分别选用亚洲排放源清单INTEX-B(Intercontinental Chemical Transport Experiment-Phase B)、REASv2.1(Regional Emission inventory in Asia version 2.1)以及全球排放源清单HTAP_v2(Hemispheric Transport of Air Pollution version 2),对浙江省2013年12月进行模拟,分别记为IN、RE和HT试验,研究人为源排放清单对大气污染物浓度数值模拟的影响。结果表明,3组试验合理的反映出PM2.5(空气动力学当量直径小于等于2.5μm的颗粒物,即细颗粒物)、PM10(空气动力学当量直径小于等于10μm的颗粒物,即可吸入颗粒物)和NO_2近地面浓度的时空分布特征,相关系数为0.5~0.8,85%以上的模拟值落在观测值的0.5~2倍范围内,但对SO_2近地面浓度模拟较差。IN、RE、HT试验对PM2.5和PM10的模拟偏差均成递减趋势,约为30%、16%和6%,HT试验的模拟值更加接近观测。INTEX-B清单中PM2.5的一次排放与二次气溶胶前提物SO_2均高于REAS与HTAP清单,因此会导致更多的硫酸盐生成,从而进一步增加PM2.5浓度。HTAP_v2清单中较低的NH3排放会抑制硝酸盐的生成,从而有助于降低PM2.5浓度。3个清单的基准年与模拟年的差异对SO_2浓度模拟的准确性影响更大,INTEX-B清单中SO_2排放量明显高于REASv2.1与HTAP_v2清单,尤其在浙北和沿海工业发达地区,导致IN试验模拟的SO_2在这些地区存在明显高估。3组试验模拟的NO_2浓度偏差最小且更为接近(-8%~4%),主要原因是3个清单在浙江省的NOx排放十分一致。从3组试验结果之间的差异程度来看,浙江省范围内PM2.5、PM10、SO_2和NO_2逐日浓度模拟值之间的平均差异程度分别约为14%、15%、51%和16%,最大差异程度分别为69%、78%、137%和132%。月均浓度与逐日浓度的平均差异程度基本一致,但最大差异程度明显更低。总体来看3组试验模拟的PM2.5、PM10与NO_2的差异程度明显低于SO_2。     

Measurements of Trace Gases in the Inflow of South China Sea Background Air and Outflow of Regional Pollution at Tai O, Southern China

We present a 16-month record of ozone (O₃), carbon monoxide (CO), total reactive nitrogen (NO_y), sulphur dioxide (SO₂), methane (CH₄), C₂ – C₈ non-methane hydrocarbons (NMHCs), C₁ – C₂ halocarbons, and dimethyl sulfide (DMS) measured at a southern China coastal site. The study aimed to establish/update seasonal profiles of chemically active trace gases and pollution tracers in subtropical Asia and to characterize the composition of the `background' atmosphere over the South China Sea (SCS) and of pollution outflow from the industrialized Pearl River Delta (PRD) region and southern China. Most of the measured trace gases of anthropogenic origin exhibited a winter maximum and a summer minimum, while O₃ showed a maximum in autumn which is in contrast to the seasonal behavior of O₃ in rural eastern China and in many mid-latitude remote locations in the western Pacific. The data were segregated into two groups representing the SCS background air and the outflow of regional continental pollution (PRD plus southern China), based on CO mixing ratios and meteorological conditions. NMHCs and halocarbon data were further analyzed to examine the relationships between their variability and atmospheric lifetime and to elucidate the extent of atmospheric processing in the sampled air parcels. The trace gas variability (S) versus lifetime (τ) relationship, defined by the power law, S_lnx = Aτ^{− b}, (where X is the trace gas mixing ratio) gives a fit parameter A of 1.39 and exponent b of 0.42 for SCS air, and A of 2.86 and b of 0.31 for the regional continental air masses. An examination of ln[n-butane]/ln[ethane] versus ln[propane]/ln[ethane] indicates that their relative abundance was dominated by mixing as opposed to photochemistry in both SCS and regional outflow air masses. The very low ratios of ethyne/CO, propane/ethane and toluene/benzene suggest that the SCS air mass has undergone intense atmospheric processing since these gases were released into the atmosphere. Compared to the results from other polluted rural sites and from urban areas, the large values of these species in the outflow of PRD/southern China suggest source(s) emitting higher levels of ethyne, benzene, and toluene, relative to light alkanes. These chemical characteristics could be unique indicators of anthropogenic emissions from southern China.     

Characterization of aerosol optical depth, aerosol mass concentration, UV irradiance and black carbon aerosols over Indo-Gangetic plains, India, during fog period

Every year during winter months (December?CJanuary) fog formation over Indo-Gangetic plains (IGP) of Indian region is believed to create numerous hazards. The present study addresses variations in aerosol optical properties, aerosol mass concentration and their impact on solar irradiance for pre-during-post fog conditions of December 2004 over IGP, India. Continuous measurements on aerosol optical depth (AOD), total aerosol mass concentration, black carbon (BC) aerosols, UV_ery and UVA were carried out for pre, during and post fog periods over study site of Allahabad, India, during December 2004 as a part of Aerosol Land Campaign-II conducted by Indian Space Research Organization (ISRO). High aerosol mass concentrations were observed during fog and post-fog periods. Accumulation mode particle loading was found to be high during pre-fog period and coarse mode particle loading was observed to be high during fog and post-fog periods. Considerable reduction in UV_ery and UVA irradiance was observed during fog period compared with pre and post-fog periods. Analysis of NOAA-HYSPLIT model runs suggested that enhanced biomass burning episodes down-wind to the study area increased the concentration of AOD and BC.     

Variations in CO,O<Subscript>3</Subscript> and black carbon aerosol mass concentrations associated with planetary boundary layer (PBL) over tropical urban environment in India

Carbon monoxide (CO), Ozone (O₃) and Black Carbon (BC) aerosol mass concentrations in relation to planetary boundary layer (PBL) height measurements were analyzed from January–December, 2008 over tropical urban environment of Hyderabad, India. DMSP-OLS night-time satellite data were analyzed for fire occurrence over the region and its correlation with pollution concentrations over the urban region. Results of the study suggested considerable increase in CO and BC concentrations during early morning hours. Higher concentration of BC, CO and ozone was observed during pre-monsoon, post-monsoon and winter and lowest concentrations exhibited during monsoon season. NCEP/NCAR reanalysis winds suggested long range transport of aerosols and trace gases from forest fires are enhancing the pollutant concentrations over the study area.     

An experimental investigation of Arctic haze at Alert,N.W.T., March 1985

Abstract

Arctic haze has been attributed to industrial pollution released at mid‐latitudes. Our current understanding has been pieced together from routine meteorological data, ground‐based air chemistry observations and limited aircraft measurements. This study investigates the relationship between synoptic boundary‐layer meteorology and the composition of the near‐surface atmosphere during the polar sunrise at Alert, N.W.T. A secondary objective is to characterize the influence of local activity on the atmospheric composition at a site for a new baseline monitoring station and at a location where aerosol chemistry and grab‐flask samples for CO₂ have been made for many years. Detailed measurements of the vertical distribution of aerosols were obtained from an upward‐looking lidar to complement the ground‐based measurements. Meteorological profiles of the near‐surface boundary layer were obtained from both free‐flying and tethered balloons. Near‐surface measurements were made of aerosol physical and chemical properties, O₃, NO₂, NO/NO_x, Peroxyacetylnitrate (PAN) and hydrocarbons.

The study period was characterized by prolonged periods with strong surface inversions, which were broken up occasionally by intrusions of cold air into the warmer air aloft. Lidar observations showed that ice crystals often accompanied aerosols and were responsible for reducing visibility below 30–40 km. There was a strong correlation between aerosol mass in the diameter size range 0.15 to 1.5 μm and total SO₄ ⁼ . PAN found at concentrations of about 200 ppt(v) was the main carrier of atmospheric nitrogen. Aerosol trace elements were divisible into anthropogenic soil, mixed soil/anthropogenic sea salt and halogens. Vertical transport in the surface boundary layer, as regulated by the strength of the surface radiation inversion, may play an important role in influencing the chemical composition of the air at the ground. The location of the new baseline monitoring laboratory was found to be generally windier and warmer than the lower altitude weather station, and the influence of local activity was found to be minimal.     

Influence of atmospheric pollutants on cloud microphysics and rainfall

For investigating the physical reasons for the observed increase in rainfall, field observational programmes have been undertaken in the upwind and downwind of industrial complexes of the Bombay region. During these programmes, surface observations of trace gases ( SO₂ and NO_x), giant size hygroscopic and nonhygroscopic aerosols and rain water samples have been made in the years 1972, 1973 and 1974. Aircraft observations of trace gases (SO₂ and NH₃), giant size aerosols, cloud condensation nuclei as well as of cloud liquid water content, cloud droplet spectra and temperature have been made on limited days during August 1974. Results of the analysis of the surface and aircraft observations have indicated that the chemical, thermal and microphysical conditions of clouds are markedly different in the upwind and downwind regions of the industrial complexes in the Bombay region. It is hypothesised that observed increase in rainfall in the region following the industrialisation is due to the differences in the chemical and physical conditions in the downwind clouds.     

中国实施铁路电气化的节能减排量估算

基于中国铁路部门逐年统计数据,计算了1975-2007年中国电气化铁路带来的逐年节能量和CO2、烟尘、SO2、CO、NOx与CnHm的直接减排量,并分析了其变化特点.结果表明,33年来电气化铁路使得中国铁路运输行业年均节省123.0万t标准煤的能源消耗,节能量年均增长13.9万t标准煤;CO2、烟尘、SO2、CO、NO...     

Study on water-soluble ionic composition of PM10 and related trace gases over Bay of Bengal during W_ICARB campaign

Aerosol (PM₁₀) samples were collected and its precursor gases, i.e., NH₃, NO, NO₂, and SO₂ measured over Bay of Bengal (BoB) during winter months of December 2008 to January 2009 to understand the relationship between particular matter (PM) and precursor gases. The observations were done under the winter phase of Integrated Campaign on Aerosols, gases and Radiation Budget (W_ICARB). The distribution of water-soluble inorganic ionic composition (WSIC) and its interaction with precursor gases over BoB are reported in present case. Average atmospheric concentration of NH₃, NO, NO_2, and SO₂ were recorded as 4.78?±?1.68, 1.89?±?1.26, 0.31?±?0.14, and 0.80?±?0.30?μg?m^?3, whereas WSIC component of PM₁₀, i.e., NH₄ ⁺, SO₄ ^2?, NO₃ ^?, and Cl^? were recorded as 1.96?±?1.66, 8.68?±?3.75, 1.92?±?1.75, and 2.48?±?0.78?μg?m^?3, respectively. In the present case, abundance of nss-SO₄ ^2? in the particulate matter is recorded as 18?%. It suggests the possibility of long-range transport as well as marine biogenic origin. Higher SO₄ ^2?/(SO₂?+?SO₄ ^2?) equivalent molar ratio during the campaign indicates the gas-to-particle conversion with great efficiency over the study region.     

Chemical composition of rain water and influence of airmass trajectories at a rural site in an ecological sensitive area of Western Ghats (India)

Samples of rain water were collected during monsoon season (June to September) of 2006 and 2007 at Hudegadde, a rural site located in an ecological sensitive area of Western Ghats. The collected samples were analyzed for pH, conductivity and major ions. At this site, rainwater pH varied from 4.20 to 7.39 with 5.65 as volume weighed mean. The observed mean was slightly lower than the average pH reported at most of the Indian continental sites. Monthly variation showed that average pH of rain water was the lowest during September (end of monsoon) and the highest during July (peak of monsoon). Overall, marine sources had dominating influence at this site. However, significant influence of anthropogenic and crustal sources from local as well as inter-continental regions was also noticed. As compared to NO₃⁻, higher concentration of SO₄²⁻ was noticed which might be due to contribution from industrial activities responsible for SO₂ emission. At this site, influence of five types of airmass trajectories was noticed i.e. i) C.I.O. (Central part of Indian Ocean)-when air masses blown from Maldives and nearby region of central Indian ocean. These airmasses had higher concentrations of nss Ca²⁺ which did not show any adverse impact on the pH; ii) N.W.I.O.(North-West Indian Ocean)-when airmasses travelled from oceanic region close to north-east Africa. These airmassses had higher concentrations of nss sulphate and nitrate and gave rise to acid rain; iii) S.W.I.O. (South -West Indian Ocean)- when airmasses came from southern part of Indian ocean (close to Mauritius). During these airmasses, rain water samples had almost equal ratio of nss SO₄²⁻ and nss Ca²⁺ similar to N.W.I.O but very low NO₃⁻ ; iv) Gulf-when airmasses were observed coming from Gulf region. Although these airmasses contributed only 2% of the total number of samples but carried high amount of nss SO₄²⁻ which gave rise to acid rain. The second lowest pH was observed during these airmasses which might be due to very high nssSO₄²⁻/nssCa²⁺ ratios; v) N.W.I.O. + S.W.I.C. (North-West Indian Ocean+South-West Indian Continental)- when airmasses originated from north-west Indian Ocean travelling towards south continental part of India and then arriving to the site. During these airmasses, samples showed typical influence of urban activities having high concentrations of nss SO₄²⁻ and NO₃⁻ leading to the lowest pH of rain water.