S. K. Sharma, T. K. Mandal, A. Sharma, Saraswati, Srishti Jain
{"title":"2010-2017年印度德里特大城市PM10碳质物种的季节和年趋势","authors":"S. K. Sharma, T. K. Mandal, A. Sharma, Saraswati, Srishti Jain","doi":"10.1007/s10874-018-9379-y","DOIUrl":null,"url":null,"abstract":"<p>PM<sub>10</sub> samples were collected to characterize the seasonal and annual trends of carbonaceous content in?PM<sub>10</sub> at an urban site of megacity Delhi, India from January 2010 to December 2017. Organic carbon (OC) and elemental carbon (EC) concentrations were quantified by thermal-optical transmission (TOT) method of PM<sub>10</sub> samples collected at Delhi. The average concentrations of PM<sub>10</sub>, OC, EC and TCA (total carbonaceous aerosol) were 222?±?87 (range: 48.2–583.8?μg?m<sup>?3</sup>), 25.6?±?14.0 (range: 4.2–82.5?μg?m<sup>?3</sup>), 8.7?±?5.8 (range: 0.8–35.6?μg?m<sup>?3</sup>) and 54.7?±?30.6?μg?m<sup>?3</sup> (range: 8.4–175.2?μg?m<sup>?3</sup>), respectively during entire sampling period. The average secondary organic carbon (SOC) concentration ranged from 2.5–9.1 μg?m<sup>?3</sup> in PM<sub>10</sub>, accounting from 14 to 28% of total OC mass concentration of PM<sub>10</sub>. Significant seasonal variations were recorded in concentrations of PM<sub>10</sub>, OC, EC and TCA with maxima during winter and minima during monsoon seasons. In the present study, the positive linear trend between OC and EC were recorded during winter (<i>R</i><sup><i>2</i></sup>?=?0.53), summer (<i>R</i><sup><i>2</i></sup>?=?0.59) and monsoon (<i>R</i><sup><i>2</i></sup>?=?0.78) seasons. This behaviour suggests the contribution of similar sources and common atmospheric processes in both the fractions. OC/EC weight?ratio suggested that vehicular emissions, fossil fuel combustion and biomass burning could be the major sources of carbonaceous aerosols of PM<sub>10</sub> at the megacity Delhi, India. Trajectory analysis indicates that the air mass approches to the sampling site is mainly from Indo Gangetic plain (IGP) region (Uttar Pradesh, Haryana and Punjab etc.), Thar desert, Afghanistan, Pakistan and surrounding areas.</p>","PeriodicalId":611,"journal":{"name":"Journal of Atmospheric Chemistry","volume":"75 3","pages":"305 - 318"},"PeriodicalIF":3.0000,"publicationDate":"2018-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s10874-018-9379-y","citationCount":"22","resultStr":"{\"title\":\"Seasonal and annual trends of carbonaceous species of PM10 over a megacity Delhi, India during 2010–2017\",\"authors\":\"S. K. Sharma, T. K. Mandal, A. Sharma, Saraswati, Srishti Jain\",\"doi\":\"10.1007/s10874-018-9379-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>PM<sub>10</sub> samples were collected to characterize the seasonal and annual trends of carbonaceous content in?PM<sub>10</sub> at an urban site of megacity Delhi, India from January 2010 to December 2017. Organic carbon (OC) and elemental carbon (EC) concentrations were quantified by thermal-optical transmission (TOT) method of PM<sub>10</sub> samples collected at Delhi. The average concentrations of PM<sub>10</sub>, OC, EC and TCA (total carbonaceous aerosol) were 222?±?87 (range: 48.2–583.8?μg?m<sup>?3</sup>), 25.6?±?14.0 (range: 4.2–82.5?μg?m<sup>?3</sup>), 8.7?±?5.8 (range: 0.8–35.6?μg?m<sup>?3</sup>) and 54.7?±?30.6?μg?m<sup>?3</sup> (range: 8.4–175.2?μg?m<sup>?3</sup>), respectively during entire sampling period. The average secondary organic carbon (SOC) concentration ranged from 2.5–9.1 μg?m<sup>?3</sup> in PM<sub>10</sub>, accounting from 14 to 28% of total OC mass concentration of PM<sub>10</sub>. Significant seasonal variations were recorded in concentrations of PM<sub>10</sub>, OC, EC and TCA with maxima during winter and minima during monsoon seasons. In the present study, the positive linear trend between OC and EC were recorded during winter (<i>R</i><sup><i>2</i></sup>?=?0.53), summer (<i>R</i><sup><i>2</i></sup>?=?0.59) and monsoon (<i>R</i><sup><i>2</i></sup>?=?0.78) seasons. This behaviour suggests the contribution of similar sources and common atmospheric processes in both the fractions. OC/EC weight?ratio suggested that vehicular emissions, fossil fuel combustion and biomass burning could be the major sources of carbonaceous aerosols of PM<sub>10</sub> at the megacity Delhi, India. Trajectory analysis indicates that the air mass approches to the sampling site is mainly from Indo Gangetic plain (IGP) region (Uttar Pradesh, Haryana and Punjab etc.), Thar desert, Afghanistan, Pakistan and surrounding areas.</p>\",\"PeriodicalId\":611,\"journal\":{\"name\":\"Journal of Atmospheric Chemistry\",\"volume\":\"75 3\",\"pages\":\"305 - 318\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2018-11-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1007/s10874-018-9379-y\",\"citationCount\":\"22\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Atmospheric Chemistry\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10874-018-9379-y\",\"RegionNum\":4,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Atmospheric Chemistry","FirstCategoryId":"89","ListUrlMain":"https://link.springer.com/article/10.1007/s10874-018-9379-y","RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Seasonal and annual trends of carbonaceous species of PM10 over a megacity Delhi, India during 2010–2017
PM10 samples were collected to characterize the seasonal and annual trends of carbonaceous content in?PM10 at an urban site of megacity Delhi, India from January 2010 to December 2017. Organic carbon (OC) and elemental carbon (EC) concentrations were quantified by thermal-optical transmission (TOT) method of PM10 samples collected at Delhi. The average concentrations of PM10, OC, EC and TCA (total carbonaceous aerosol) were 222?±?87 (range: 48.2–583.8?μg?m?3), 25.6?±?14.0 (range: 4.2–82.5?μg?m?3), 8.7?±?5.8 (range: 0.8–35.6?μg?m?3) and 54.7?±?30.6?μg?m?3 (range: 8.4–175.2?μg?m?3), respectively during entire sampling period. The average secondary organic carbon (SOC) concentration ranged from 2.5–9.1 μg?m?3 in PM10, accounting from 14 to 28% of total OC mass concentration of PM10. Significant seasonal variations were recorded in concentrations of PM10, OC, EC and TCA with maxima during winter and minima during monsoon seasons. In the present study, the positive linear trend between OC and EC were recorded during winter (R2?=?0.53), summer (R2?=?0.59) and monsoon (R2?=?0.78) seasons. This behaviour suggests the contribution of similar sources and common atmospheric processes in both the fractions. OC/EC weight?ratio suggested that vehicular emissions, fossil fuel combustion and biomass burning could be the major sources of carbonaceous aerosols of PM10 at the megacity Delhi, India. Trajectory analysis indicates that the air mass approches to the sampling site is mainly from Indo Gangetic plain (IGP) region (Uttar Pradesh, Haryana and Punjab etc.), Thar desert, Afghanistan, Pakistan and surrounding areas.
期刊介绍:
The Journal of Atmospheric Chemistry is devoted to the study of the chemistry of the Earth''s atmosphere, the emphasis being laid on the region below about 100 km. The strongly interdisciplinary nature of atmospheric chemistry means that it embraces a great variety of sciences, but the journal concentrates on the following topics:
Observational, interpretative and modelling studies of the composition of air and precipitation and the physiochemical processes in the Earth''s atmosphere, excluding air pollution problems of local importance only.
The role of the atmosphere in biogeochemical cycles; the chemical interaction of the oceans, land surface and biosphere with the atmosphere.
Laboratory studies of the mechanics in homogeneous and heterogeneous transformation processes in the atmosphere.
Descriptions of major advances in instrumentation developed for the measurement of atmospheric composition and chemical properties.