| 1. |
- Bisht, D. S., et al.
(författare)
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Tethered balloon-born and ground-based measurements. of black carbon and particulate profiles within the lower troposphere during the foggy period in Delhi, India
- 2016
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Ingår i: Science of the Total Environment. - : Elsevier BV. - 0048-9697 .- 1879-1026. ; 573, s. 894-905
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Tidskriftsartikel (refereegranskat)abstract
- The ground and vertical profiles of particulate matter (PM) were mapped as part of a pilot study using a Tethered balloon within the lower troposphere (1000 m) during the foggy episodes in the winter season of 2015-16 in New Delhi, India. Measurements of black carbon (BC) aerosol and PM <2.5 and 10 mu m (PM2.5 &PM-10 respectively) concentrations and their associated particulate optical properties along with meteorological parameters were made. The mean concentrations of PM2.5, PM10, BC370 (nm), and BC880 nm were observed to be 146.8 +/- 42.1, 245.4 +/- 65.4, 30.3 +/- 122, and 24.1 +/- 103 mu g m(-3), respectively. The mean value of PM2.5 was similar to 12 times higher than the annual US-EPA air quality standard. The fraction of BC in PM2.5 that contributed to absorption in the shorter visible wavelengths (BC370 nm) was-21%. Compared to clear days, the ground level mass concentrations of PM2.5 and BC370 nm particles were substantially increased (59% and 24%, respectively) during the foggy episode. The aerosol light extinction coefficient (sigma(ext)) value was much higher (mean: 610 Mm(-1)) during the lower visibility (foggy) condition. Higher concentrations of PM2.5 (89 mu g m(-3)) and longer visible wavelength absorbing BC880 am (25.7 mu g m(-3)) particles were observed up to 200 m. The BC880 nm and PM2.5 aerosol concentrations near boundary layer (1 km) were significantly higher (similar to 1.9 and 12 mu g m(-3)), respectively. The BC (i.e BCtot) aerosol direct radiative forcing (DRF) values were estimated at the top of the atmosphere (TOA), surface (SFC), and atmosphere (ATM) and its resultant forcing were- 75.5 Wm(-2) at SFC indicating the cooling effect at the surface. A positive value (20.9 Wm(-2)) of BC aerosol DRF at TOA indicated the warming effect at the top of the atmosphere over the study region. The net DRF value due to BC aerosol was positive (96.4 Wm(-2)) indicating a net warming effect in the atmosphere. The contribution of fossil and biomass fuels to the observed BC aerosol DRF values was -78% and-22%, respectively. The higher mean atmospheric heating rate (2.71 K clay(-1)) by BC aerosol in the winter season would probably strengthen the temperature inversion leading to poor dispersion and affecting the formation of clouds. Serious detrimental impacts on regional climate due to the high concentrations of BC and PM (especially PM2.5) aerosol are likely based on this study and suggest the need for immediate, stringent measures to improve the regional air quality in the northern India.
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| 2. |
- Rao, P. S. P., et al.
(författare)
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Sources of chemical species in rainwater during monsoon and non-monsoonal periods over two mega cities in India and dominant source region of secondary aerosols
- 2016
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310 .- 1873-2844. ; 146, s. 90-99
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Tidskriftsartikel (refereegranskat)abstract
- Samples of rainwater (RW) were collected to characterize the chemistry and sources in two representative megacities at Pune (Southwest) and Delhi (Northern) India from 2011 to 2014 across two seasons: monsoon (MN) and non-monsoon (NMN). Collected RW samples were analyzed for major chemical constituents (F-, Cl-, SO42-, NO3-, NH4+, Na+, K+, Ca2+, and Mg2+), pH and conductivity. In addition, bicarbonate (HCO3-) was also estimated. The mean pH values of the RW were >6 at Pune and <6 at Delhi and 4% and 26% were acidic, respectively. The mean sum of all measured ionic species in Pune and Delhi was 304.7 and 536.4 mu ep/l, respectively, indicating that significant atmospheric pollution effects in these Indian mega cities. Both the Ca2+ and SO42- were the dominant ions, accounting for 43% (Pune) and 54% (Delhi) of the total ions. The sum of measured ions during the NMN period was greater than the NM period by a factor of 1.5 for Pune (278.4: NM and 412.1: NMN mu eq/l) and a factor of about 2.5 for Delhi (406 and 1037.7 mu eq/l). The contributions of SO42- and NO3- to the RW acidity were similar to 40% and 60%, respectively, at Pune and correspondingly, 36% and 64% at Delhi. The concentrations of secondary aerosols (SO42- and NO3-) were higher by a factor of two and three when the air masses were transported to Pune from the continental side. At Delhi, the concentrations of SO42-, NO3-, Ca2+, and Mg2+ were significantly higher when the air masses arrive from Punjab, Haryana, and Pakistan indicating the greater atmospheric pollution over the Indo-Gangetic Plain. Positive matrix factorization was applied to the source apportionment of the deposition fluxes of these ions. Three factors were obtained for Pune and four for Delhi. The sources at Pune were secondary aerosols from fossil fuel combustion, soil dust, and marine, whereas, at Delhi, the sources were soil, fossil fuel combustion, biomass burning, and industrial chlorine.
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| 3. |
- Brauer, M., et al.
(författare)
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Ambient Air Pollution Exposure Estimation for the Global Burden of Disease 2013
- 2016
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Ingår i: Environmental Science & Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 50:1, s. 79-88
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Tidskriftsartikel (refereegranskat)abstract
- Exposure to ambient air pollution is a major risk factor for global disease. Assessment of the impacts of air pollution on population health and evaluation of trends relative to other major risk factors requires regularly updated, accurate, spatially resolved exposure estimates. We combined satellite-based estimates, chemical transport model simulations, and ground measurements from 79 different countries to produce global estimates of annual average fine particle (PM2.5) and ozone concentrations at 0.1 degrees X 0.1 degrees spatial resolution for five-year intervals from 1990 to 2010 and the year 2013. These estimates were applied to assess population-weighted mean concentrations for 1990-2013 for each of 188 countries. In 2013, 87% of the world's population lived in areas exceeding the World Health Organization Air Quality Guideline of 10 mu g/m(3) PM2.5 (annual average). Between 1990 and 2013, global population-weighted PM2.5 increased by 20.4% driven by trends in South Asia, Southeast Asia, and China. Decreases in population-weighted mean concentrations of PM2.5 were evident in most high income countries. Population-weighted mean concentrations of ozone increased globally by 8.9% from 1990-2013 with increases in most countries-except for modest decreases in North America, parts of Europe, and several countries in Southeast Asia.
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| 4. |
- Tiwari, Suresh, et al.
(författare)
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Atmospheric heating due to black carbon aerosol during the summer monsoon period over Ballia : A rural environment over Indo-Gangetic Plain
- 2016
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Ingår i: Atmospheric research. - : Elsevier BV. - 0169-8095 .- 1873-2895. ; 178, s. 393-400
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Tidskriftsartikel (refereegranskat)abstract
- Black carbon (BC) aerosols are one of the most uncertain drivers of global climate change. The prevailing view is that BC mass concentrations are low in rural areas where industrialization and vehicular emissions are at a minimum. As part of a national research program called the Ganga Basin Ground Based Experiment-2014 under the Cloud Aerosol Interaction and Precipitation Enhancement Experiment (CAIPEEX) Phase-III of Ministry of Earth Sciences, Government of India, the continuous measurements of BC and particulate matter (PM) mass concentrations, were conducted in a rural environment in the highly-polluted Indo-Gangetic Plain region during 16th June to 15th August (monsoon period), 2014. The mean mass concentration of BC was 4.03 (+/- 0.85) mu g m(-3) with a daily variability between 2.4 and 5.64 mu g m(-3), however, the mean mass PM concentrations [near ultrafine (PM1.0), fine (PM2.5) and inhalable (PM1.0)] were 29.1(+/- 16.2), 34.7 (+/- 19.9) and 43.7 (+/- 283) mu g m(-3), respectively. The contribution of BC in PM1.0 was approximately 13%, which is one of the highest being recorded. Diurnally, the BC mass concentrations were highest (mean: 5.89 mu g m(-3)) between 20:00 to 22:00 local time (LT) due to the burning of biofuels/biomass such as wood, dung, straw and crop residue mixed with dung by the local residents for cooking purposes. The atmospheric direct radiative forcing values due to the composite and BC aerosols were determined to be +78.3, +44.9, and +45.0 W m(-2) and +42.2, +35.4 and +34.3 W m(-2) during the months ofJune, July and August, respectively. The corresponding atmospheric heating rates (AHR) for composite and BC aerosols were 2.21,1.26 and 1.26; and 1.19, 0.99 and 0.96 K day(-1) for the month ofJune, July and August, respectively, with a mean of 1.57 and 1.05 K day(-1) which was 33% lower AHR (BC) than for the composite particles during the study period. This high AHR underscores the importance of absorbing aerosols such as BC contributed by residential cooking using biofuels in India. Our study demonstrates the need for immediate, effective regulations and policies that mitigate the emission of BC particles from domestic cooking in rural areas of India.
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| 5. |
- Sundqvist, Kristina, et al.
(författare)
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Receptor Modeling of PCDD/FS in Sediment of the Sundsvall Bay, Sweden
- 2008
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Ingår i: Organohalogen Compounds. ; 70:1641-4
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Tidskriftsartikel (refereegranskat)abstract
- In the Sundsvall Bay area, located in the southern Bothnian Sea (a sub-basin of the Baltic Sea), industrial history have included a large variety of activities, from small sawmills to large pulp and paper mills as well as chloralkali production. Previously, several sawmills in the area used chlorophenol formulations for wood preservation, and these were contaminated by PCDD/Fs. Chloralkali production using graphite electrodes and bleaching of pulp using chlorine are manufacturing processes also known to have caused PCDD/Fs emissions. A chemical industry has been active in the area since the 1930s and an aluminum smelter was built in 1942. Aluminum production, like many high temperature processes, is known to produce PCDD/Fs.The aim of this study was to investigate the possibility of using receptor modeling for identification and apportioning of the major sources of PCDD/Fs in the Sundsvall Bay. The Sundsvall Bay was chosen as the first study area of this modeling technique along the Swedish coast since there are several possible sources of PCDD/Fs in the area and a relatively large number of sediment samples have been analyzed. Current PCDD/F emissions have been investigated by sampling river water, industrial effluent entering the bay and, in addition, soil from two contaminated sawmill sites.
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