Source apportionment in oil spill remediation

A pipe rupture during unloading led to a spillage of 350-700 tonnes of Ca?o Limon, a light sweet crude oil, into San Vicente Bay in 2007. Initial clean-up methods removed the majority of the oil from the sandy beaches although some oil remained on the rocky shores. It was necessary for the responsible party to clean the spilled oil even though at this location there were already crude oil hydrocarbons from previous industrial activity. A biosolvent based on vegetable oil derivatives was used to solubilise the remaining oil and a statistical approach to source apportionment was used to determine the efficacy of the cleaning. Sediment and contaminated rock samples were taken prior to cleaning and again at the same locations two days after application of the biosolvent. The oil was extracted using a modified USEPA Method 3550B. The alkanes were quantified together with oil biomarkers on a GC-MS. The contribution that Ca?o Limon made to the total oil hydrocarbons was calculated from a Partial Least Squares (PLS) analysis using Ca?o Limon crude oil as the source. By the time the biosolvent was applied, there had already been some attenuation of the oil with all alkanes 相似文献   

BP网络应用于大气颗粒物的源解析

应用BP网络对大气颗粒物进行源解析,将大气采集样本中的元素含量和大气颗粒物源成分谱构成训练样本集,用BP网络进行训练,由训练好的网络的权值可以计算出大气颗粒物的污染排放源的权重贡献率.将BP源解析法的计算结果与其它源解析法得到的结果比较,表明BP网络应用于大气颗粒物的源解析是可行的.     

Receptor model-based source apportionment of particulate pollution in Hyderabad, India

Air quality in Hyderabad, India, often exceeds the national ambient air quality standards, especially for particulate matter (PM), which, in 2010, averaged 82.2?±?24.6, 96.2?±?12.1, and 64.3?±?21.2 μg/m³ of PM₁₀, at commercial, industrial, and residential monitoring stations, respectively, exceeding the national ambient standard of 60 μg/m³. In 2005, following an ordinance passed by the Supreme Court of India, a source apportionment study was conducted to quantify source contributions to PM pollution in Hyderabad, using the chemical mass balance (version 8.2) receptor model for 180 ambient samples collected at three stations for PM₁₀ and PM_2.5 size fractions for three seasons. The receptor modeling results indicated that the PM₁₀ pollution is dominated by the direct vehicular exhaust and road dust (more than 60 %). PM_2.5 with higher propensity to enter the human respiratory tracks, has mixed sources of vehicle exhaust, industrial coal combustion, garbage burning, and secondary PM. In order to improve the air quality in the city, these findings demonstrate the need to control emissions from all known sources and particularly focus on the low-hanging fruits like road dust and waste burning, while the technological and institutional advancements in the transport and industrial sectors are bound to enhance efficiencies. Andhra Pradesh Pollution Control Board utilized these results to prepare an air pollution control action plan for the city.     

杭州市居室空气中芳香族化合物污染现状及其来源解析

用热解吸/气质联用技术研究了杭州市居室空气中芳香族化合物的组成。结果表明,杭州市居室空气中共存在60种芳香族化合物,其中苯系化合物48种,非苯芳香族化合物12种,检出率大于50%的23种;苯、甲苯、乙苯、苯乙烯、邻二甲苯、间(对)-二甲苯等10种化合物的总含量之和大于85.39%,是室内空气中主要的芳香族污染物,除萘外,其他22种污染物的平均浓度值均随装修时间间隔延长而降低;污染物主要来源是室内装修过程中使用的或装修材料中残留的有机溶剂、机动车辆排放的尾气、居民家庭中常用的清洁用品及含萘等成分的防蛀剂。     

Source apportionment of polycyclic aromatic hydrocarbons in the Dahuofang Reservoir, Northeast China

Polycyclic aromatic hydrocarbons (PAHs) in 24 surface sediments from the Dahuofang Reservoir (DHF), the largest man-made lake in Northeast China, were measured. The results showed that the concentrations of 16 US EPA priority PAHs in the sediments ranged from 323 to 912 ng/g dry weight with a mean concentration of 592?±?139 ng/g. The PAH source contributions were estimated based on positive matrix factorization model. The coal combustion contributed to 31 % of the measured PAHs, followed by residential emissions (22 %), biomass burning (21 %), and traffic-related emissions (10 %). Pyrogenic sources contributed ～84 % of anthropogenic PAHs to the sediments, indicating that energy consumption release was a predominant contribution of PAH pollution in DHF. Compared with the results from the urban atmospheric PAHs in the region, there was a low contribution from traffic-related emissions in the sediments possibly due to the low mobility of the traffic-related derived 5+6-ring PAHs and their rapid deposition close to the urban area.     

Estimated distributions of personal exposure to respirable particles

A method of estimating distributions of exposure to respirable particles is presented. Using pollutant monitoring data from outdoors and indoors, time-activity data and a time-weighted exposure model, means and variances for exposure distributions are generated. Variances are estimated using Gauss' law of error propagation. The model is calibrated using data from a personal monitoring study. Estimated distributions of exposure to respirable particles for children in six cities living in homes with and without smokers are presented. The implications of these estimates for air pollution epidemiology and needs for further research are discussed.     

Chemistry of fogs at Agra, India: Influence of soil particulates and atmospheric gases

Fog water samples were collected in the months of December and January during 1998–2000 at Agra, India. The samples were analyzed for pH, major anions (F⁻, Cl⁻, SO₄ ²⁻, NO₃ ⁻, HCOO⁻ and CH₃COO⁻), major cations (Ca²⁺, Mg²⁺, Na⁺ and K⁺) and NH₄ ⁺ using ion chromatography, ICP-AES and spectrophotometer methods, respectively. pH of fog water samples ranged between 7.0 and 7.6 with a volume weighted mean of 7.2, indicating its alkaline characteristic. NH₄ ⁺ contributed 40%, SO₄ ²⁻ and NO₃ ⁻ accounted for 28%, while Ca²⁺, Mg²⁺, Na⁺ and K⁺ accounted for 16% of the total ionic concentration. The ratios of Mg²⁺/Ca²⁺ and Na⁺/Ca²⁺ in fog water indicates that 50–75% of fog water samples correspond to the respective ratios in local soil. Significant correlation between Ca²⁺, Mg²⁺, Na⁺ and K⁺ suggests their soil origin. The order of neutralization, NH₄ ⁺ (1.4) > Ca²⁺ (0.28) > Mg²⁺ (0.12), indicates that NH₄ ⁺ is the major neutralizing species. Fog water and atmospheric alkalinity were also computed and were found to be 873 and 903 neqm⁻³, respectively. Both of these values are higher than values reported from temperate sites and thus indicate that at the present level of pollutants, there is no risk of acid fog problem. The study also shows that the alkaline nature of fog water is due to dissolution of ammonia gas and partly due to interaction of fog water with soil derived aerosols.     

Viable fungi and bacteria in personal exposure samples in relation to microenvironments

Personal exposures to viable fungi and bacteria were compared with the concentrations being assessed by stationary samplers in home and workplace microenvironments. A random sample of 81 elementary school teachers in eastern Finland performed two 24-hour measurement periods in wintertime. Concentrations and prevalences of viable fungi and bacteria on the collection filters were determined by cultivation method. The geometric mean concentration was 3-12 cfu m(-3) for total viable fungi, 0.6-3.7 cfu m(-3) for Penicillium and mainly under 1 cfu m(-3) for other fungi. The samples with higher fungal concentrations also had higher diversity of fungi than samples with lower concentrations. The total number of fungal genera recovered was 39 for personal, 34 for home and 23 for work samples. The variation in concentration of Penicillium explained even 25-95% of the variations of total fungal concentration in personal exposure, home and workplace environments. There was an association between personal exposure and home concentration of viable fungi and between personal exposure and home and work concentrations of viable bacteria. Personal exposure and home concentrations of fungi were higher in rural areas than in urban areas. Our results also indicate that presence of a certain fungus in a microenvironment does not necessarily mean similar findings in personal exposure samples.     

Study of personal exposure to airborne respirable particles and carbon monoxide

Simultaneous measurements of CO and respirable particles (RP) at outdoor network stations and of personal exposure in a sample of twelve volunteers were carried out during the winter and summer season of 1980/81 in order to evaluate how well personal exposure can be assessed from outdoor network station data.The results have shown that personal exposure of our subjects to both CO and RP is in best correlation with exposure at home where subjects spend in the average nearly 70% of their time. While personal exposure to CO can hardly be related to outdoor CO levels, personal exposure to RP is in fair agreement with simultaneously measured outdoor concentrations in winter (but not in summer). A large intercept on WAE axis of the WAE/RP relationship indicates that a considerable part of personal exposure to RP should be attributed to particles which are not of indoor origin. This part does not follow the seasonal and day-to-day changes in outdoor RP concentration and causes a negative, but highly significant correlation between WAE/RP ratio and RP.     

Distribution of suspended particulate matter with trace element composition and apportionment of possible sources in the Raniganj coalfield,India

Ambient air monitoring for suspended particulate matter was carried over a period of one year in some coal mining areas of the Raniganj coalfield. Concentrations of seven elements in suspended particulate matter were determined. The set of data obtained was analysed to determine the sources of trace elements by factor analysis. The data could be interpreted on the basis of five factors. These factors are attributed to various sources of particulate matter by noting the dependence of factors on the elements.     

Non-occupational exposure to silica dust in vicinity of slate pencil industry, India

Biomonitoring of polycyclic aromatic hydrocarbons (PAHs) in the leaves of Calotropis gigantea R.Br. were performed at seven sites in the surrounding areas of a Thermal Power Plant (TPP), using the gas chromatography and mass spectrometry technique. The primary objective of the study was to monitor the degree of PAHs load in the nearby sites around TPP compared to distant sites. Total PAH (SigmaPAH) concentrations in the leaves ranged from 372.18 (at control site 7) to 4362.35 ng g(-1) d.w. (at highest polluted site 4). The concentration factors ranged from 2.65 to 11.72 for the sites located at 1 km to the point source and 1.0 to 7.08 for distant sites. The share of carcinogenic PAHs to the total PAHs differed with the site, ranging from 10.76% to 26.92%. The sites located closer to TPP have shown higher concentrations of medium and high molecular weight PAHs, which decreased gradually with the distance from the source. The total PAH burden at control site was dominated by the low and medium molecular weight PAHs compounds viz., naphthalene, acenaphthylene, acenaphthene, phenanthrene, fluoranthene, pyrene, chrysene, coronene., whilst at other sites medium and high PAHs viz., fluoranthene, pyrene, benzo (a) anthracene, chrysene, benzo (b) fluoranthene, benzo (e) pyrene and coronene showed the highest values. These results support the biomonitoring ability of Calotropis gigantea R.Br. leaves to monitor PAHs contamination.     

Source identification study of heavy metal contamination in the industrial hub of Unnao,India

India's Unnao region is home to many leather-treatment facilities and related industries. Industrial and agricultural waste leads to heavy metal contamination that infiltrates groundwater and leads to human health hazards. This work measured the amount of heavy metal in groundwater at specific sites near the industrial facilities in Unnao and identified potential sources of contamination as anthropogenic or lithogenic. Groundwater samples were taken from 10 bore well sites chosen for depth and proximity to industry. Data obtained from sample sites was interpreted using a multivariate statistical analytical approach, i.e., principal component analysis, clustering analysis, and correlation analysis. The results of the multivariate analysis showed that cadmium, copper, manganese, nickel, lead, and zinc were correlated with anthropogenic sources, while iron and chromium were associated with lithogenic sources. These findings provide information on the possible sources of heavy metal contamination and could be a model for assessing and monitoring heavy metal pollution in groundwater in other locales. This study analyzed a selection of heavy metals chosen on the basis of industries located in the study area, which might not provide a complete range of information about the sources and availability of all heavy metals. Therefore, an extended investigation on heavy metal fractions will be developed in further studies.     

Risk factors and prevalence of dental fluorosis and dental caries in school children of North India

The aim of the study was to assess the prevalence of dental fluorosis, dental caries, and associated risk factors in the school children of district Fatehgarh Sahib, Punjab, India, using a cross-sectional study design. Oral health status of children aged between 8 and 15 years was assessed using World Health Organization (WHO) 2013 criteria. Dental fluorosis was assessed using Dean’s index, and dental caries were recorded using decayed, missing, filled/decayed, extracted, filled (DMF/def) indices. Four hundred school children were examined, of which 207 were in the 8–11-year-old group and 193 were in the 12–15-year-old group. The overall prevalence of dental fluorosis was 4.1%, which might be linked to a high concentration of fluoride in drinking water at certain locations of rural Punjab. The prevalence of dental caries was 36.5% with a mean DMF score of 0.3 and def score of 0.6. Risk factors for dental caries include oral hygiene behavior and sugar consumption patterns. The study highlights the need to increase awareness about the oral health and hygiene among the school children in India.     

Assessment of non-occupational exposure to polycyclic aromatic hydrocarbons through personal air sampling and urinary biomonitoring

Non-occupational inhalation and ingestion exposure to polycyclic aromatic hydrocarbons (PAHs) has been studied in 8 non-smoking volunteers through personal air sampling and urinary biomonitoring. The study period was divided into 4 segments (2 days/segment), including weekdays with regular commute and weekends with limited traffic related exposures; each segment had a high or low PAH diet. Personal air samples were collected continuously from the subjects while at home, at work, and while commuting to and from work. All urine excretions were collected as individual samples during the study. In personal air samples, 28 PAHs were measured, and in urine samples 9 mono-hydroxylated metabolites (OH-PAHs) from 4 parent PAHs (naphthalene, fluorene, phenanthrene and pyrene) were measured. Naphthalene was found at higher concentrations in air samples collected at the subjects' residences, whereas PAHs with four or more aromatic rings were found at higher levels in samples taken while commuting. Urinary OH-PAH biomarker levels increased following reported high inhalation and/or dietary exposure. On days with a low PAH diet, the total amount of inhaled naphthalene during each 24-hour period was well correlated with the amount of excreted naphthols, as was, to a lesser extent, fluorene with its urinary metabolites. During days with a high dietary intake, only naphthalene was significantly correlated with its excreted metabolite. These findings suggest that this group of non-occupational subjects were exposed to naphthalene primarily through indoor air inhalation, and exposed to other PAHs such as pyrene mainly through ingestion.     

Indoor exposure to respirable particulate matter and particulate-phase PAHs in rural homes in North India

In order to evaluate the exposure of the northern India rural population to polyaromatic hydrocarbon (PAH) inhalation, indoor pollution was assessed by collecting and analyzing the respirable particulate matter PM_2.5 and PM₁₀ in several homes of the village Bhithauli near Lucknow, UP. The home selection was determined by a survey. Given the nature of biomass used for cooking, homes were divided into two groups, one using all kinds of biomass and the second type using plant materials only. Indoor mean concentrations of PM_2.5 and associated PAHs during cooking ranged from 1.19 ± 0.29 to 2.38 ± 0.35 and 6.21 ± 1.54 to 12.43 ± 1.15 μg/m³, respectively. Similarly, PM₁₀ and total PAHs were in the range of 3.95 ± 1.21 to 8.81 ± 0.78 and 7.75 ± 1.42 to 15.77 ± 1.05 μg/m³, respectively. The pollutant levels during cooking were significantly higher compared to the noncooking period. The study confirmed that indoor pollution depends on the kind of biomass fuel used for cooking.     

Changes in structural attributes of plant communities along disturbance gradients in a dry deciduous forest of Western Ghats, India

Changes in tree and understory plant diversity and community composition in two sites at different disturbance levels were studied on the Anaikatty hills, Western Ghats. Systematic sampling using small scale permanent quadrates (50 x 20 m for trees, 5 x 5 m for shrubs/saplings, 1 x 1 m for herbs/seedlings) enumerated 3,376 individuals of trees (106 species), 8,599 of individuals shrubs (122 species) and 16,659 individuals of herbs (145 species). Among the two sites, species richness and diversity were highest for low disturbed stand (98 and 3.9, respectively) compared to high disturbed site (45 and 2.71, respectively). Result of cluster analysis showed that two distinct clusters were formed on the basis of disturbance of the area in concordance with our field observation. A total of 37 species were common to both sites, sixty one species exclusively found in low disturbed site and eight species were pertained to highly disturbed site. Mann-Whitney test based on Monte Carlo approximation at 95% confidence levels indicated that both populations were not entirely different. The clear difference was only observed for average basal area of trees, density of seedlings, number of species, density and diversity for shrubs and number of species and diversity for herb. The species composition were different in two stand i.e., Nothopegia racemosa-Albizia amara-Maba neilghrrensis in low disturbed stand and Albizia amara-Pleiospermium alatum-Bauhinia racemosa in high disturbed stand. The major disturbance factors identification using spearman rank correlation indicated that the disturbance in low disturbed habitats were mostly from past logging followed by cutting and illicit felling and grazing, while in high disturbed habitats, it was human presence, past logging and lopping and fuel wood collection.     

The role of secondary particulates in European emission abatement strategies

Economic assessments have indicated that the greatest benefits of reducing atmospheric emissions of sulphur and nitrogen compounds in Europe come from the resulting reductions in secondary particulate concentrations. For comparison with abatement strategies devised to reduce exceedance of critical loads for acidification, this paper, therefore, considers optimisation of emission abatement strategies to reduce secondary particulate concentrations and minimise human exposure. It is seen that this changes the relative emphasis between some countries in reducing their emissions, and also places less importance on emissions of ammonia from agriculture relative to those of SO₂ and NO_x. The effect of placing emphasis on improvement in the more highly polluted areas of Europe is also examined by imposing a threshold. The benefits of the strategies in terms of ecosystem protection and human exposure to particulates are presented for all scenarios studied. The scenarios are also interpreted in terms of a blame matrix for human exposure to secondary particulates.     

A chemosorptive cylindrical denuder designed for personal exposure measurements of isocyanates-evaluation on generated aerosols of 4,4'-methylenediphenyl diisocyanate

A denuder/filter system constructed for solvent-free personal exposure measurements was evaluated for separation of vapour and particulate 4,4'-methylenediphenyl diisocyanate (4,4'-MDI) generated from heated PUR-foam. The two different phases were collected in the denuder and on the filter, respectively, by chemosorption on a polydimethylsiloxane (SE-30)-dibutylamine (DBA) stationary phase. Both repeatability and the total mass concentration of 4,4'-MDI were similar to that obtained from the reference method, in this case an impinger/filter system. The penetration of particles through the denuder at 300 ml min(-1) was nearly 100% in the particle size range 25 to 700 nm, which fits well with the Gormley-Kennedy equation. Denuder/filter sampling of the 4,4'-MDI aerosol at 500 ml min(-1) yielded a phase distribution that was in accordance with the results from the reference method. The method limit of detection was 6 ng m(-3) and 4 ng m(-3) for the denuder and filter, respectively, when using an air sampling flow rate of 300 ml min(-1) and a sampling period of 15 min. This is well below the Swedish occupational exposure limit (OEL) of 50 and 100 microg m(-3) for an 8-hour working day and a 5-min period, respectively.     

Indoor NO2 pollution and personal exposure to NO2 in two areas with different outdoor NO2 pollution

Indoor NO₂ concentrations were measured in the kitchen, the living room and bedroom of 612 houses in two different areas in the Netherlands. In a group of housewives living in these homes, personal exposure to NO₂ was measured. NO₂ concentrations indoors were dependent on the presence or absence of (un)vented gas appliances. Personal NO₂ exposure was only different between the two areas in the group with the lowest indoor concentrations. In this study, it was determined that gas appliances inside the house are the most important factor with respect to NO₂ exposure and that outside NO₂ concentration played a secondary role, except in situations where gas appliances were absent.