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Black carbon (BC) is an important atmospheric aerosol constituent that affects the climate by absorbing (directly) the sunlight and modifying cloud characteristics (indirectly). Here, we present first time yearlong measurements of BC and carbon monoxide (CO) from an urban location of Guwahati located in the Brahmaputra River valley (BRV) in the northeast region of India from 1st July 2013 to 30th June 2014. Daily BC concentrations varied within the range of 2.86 to 11.56 mu g m(-3) with an annual average of 7.17 +/- 1.89 mu g m(-3), while, CO varied from 0.19 to 1.20 ppm with a mean value of 0.51 +/- 0.19 ppm during the study period. The concentrations of BC (8.37 mu g m(-3)) and CO (0.67 ppm) were similar to 39% and similar to 55% higher during the dry months (October to March) than the wet months (April to September) suggesting that seasonal changes in meteorology and emission sources play an important role in controlling these species. The seasonal Delta BC/Delta CO ratios were highest (lowest) in the pre-monsoon (winter) 18.1 +/- 1.4 mu g m(-3) ppmv(-1) (12.6 +/- 2.2 mu g m(-3) ppmv(-1)) which indicate the combustion of biofuel/biomass as well as direct emissions from fossil fuel during the pre-monsoon season. The annual BC emission was estimated to be 2.72 Gg in and around Guwahati which is about 44% lower than the mega city 'Delhi' (4.86 Gg). During the study period, the annual mean radiative forcing (RF) at the top of the atmosphere (TOA) for clear skies of BC was +9.5Wm(-2), however, the RF value at the surface (SFC) was -21.1 Wm(-2) which indicates the net warming and cooling effects, respectively. The highest RF at SFC was in the month of April (-30 Wm(-2)) which is coincident with the highest BC mass level. The BC atmospheric radiative forcing (ARF) was +30.16 (annualmean) Wm(-2) varying from +23.1 to +43.8 Wm(-2). The annualmean atmospheric heating rate (AHR) due to the BC aerosols was 0.86 K day(-1) indicates the enhancement in radiation effect over the study region. The Weather Research and Forecasting model coupled with Chemistry(WRF-Chem) captured the seasonal cycle of observed BC fairly well but underestimated the observed BC during the month of May-August. Model results show that BC at Guwahati is controlled mainly by anthropogenic emissions except during the pre-monsoon season when open biomass burning also makes a similar contribution. (C) 2016 Elsevier B.V. All rights reserved.

期刊论文 2016-08-15 DOI: 10.1016/j.scitotenv.2016.03.157 ISSN: 0048-9697

Particulate matter (PM2.5) samples were collected over Delhi, India during January to December 2012 and analysed for carbonaceous aerosols and inorganic ions (SO42 -and NO3-) in order to examine variations in atmospheric chemistry, combustion sources and influence of long-range transport. The PM2.5 samples are measured (offline) via medium volume air samplers and analysed gravimetrically for carbonaceous (organic carbon, OC; elemental carbon, EC) aerosols and inorganic ions (SO42 -and NO3-). Furthermore, continuous (online) measurements of PM2.5 (via Beta-attenuation analyser), black carbon (BC) mass concentration (via Magee scientific Aethalometer) and carbon monoxide (via CO-analyser) are carried out. PM2.5 (online) range from 18.2 to 500.6 mu gm(-3) (annual mean of 124.6 +/- 87.9 mu gm(-3)) exhibiting higher night-time (129.4 mu gm(-3)) than daytime (103.8 mu g m(-3)) concentrations. The online concentrations are 38% and 28% lower than the offline during night and day, respectively. In general, larger night-time concentrations are found for the BC, OC, NO3- and SO42-, which are seasonally dependent with larger differences during late post-monsoon and winter. The high correlation (R-2=0.74) between OC and EC along with the OC/EC of 7.09 (day time) and 4.55 (night-time), suggest significant influence of biomass-burning emissions (burning of wood and agricultural waste) as well as secondary organic aerosol formation during daytime. Concentrated weighted trajectory (CWT) analysis reveals that the potential sources for the carbonaceous aerosols and pollutants are local emissions within the urban environment and transported smoke from agricultural burning in northwest India during post-monsoon. BC radiative forcing estimates result in very high atmospheric heating rates (similar to 1.8-2.0 K day(-1)) due to agricultural burning effects during the 2012 post-monsoon season. (C) 2015 Elsevier B.V. All rights reserved.

期刊论文 2015-07-15 DOI: 10.1016/j.scitotenv.2015.03.083 ISSN: 0048-9697

[1] Aerosol sources, transport, and sinks are simulated, and aerosol direct radiative effects are assessed over the Indian Ocean for the Indian Ocean Experiment (INDOEX) Intensive Field Phase during January to March 1999 using the Laboratoire de Meteorologie Dynamique (LMDZT) general circulation model. The model reproduces the latitudinal gradient in aerosol mass concentration and optical depth (AOD). The model-predicted aerosol concentrations and AODs agree reasonably well with measurements but are systematically underestimated during high-pollution episodes, especially in the month of March. The largest aerosol loads are found over southwestern China, the Bay of Bengal, and the Indian subcontinent. Aerosol emissions from the Indian subcontinent are transported into the Indian Ocean through either the west coast or the east coast of India. Over the INDOEX region, carbonaceous aerosols are the largest contributor to the estimated AOD, followed by sulfate, dust, sea salt, and fly ash. During the northeast winter monsoon, natural and anthropogenic aerosols reduce the solar flux reaching the surface by 25 W m(-2), leading to 10 - 15% less insolation at the surface. A doubling of black carbon (BC) emissions from Asia results in an aerosol single-scattering albedo that is much smaller than in situ measurements, reflecting the fact that BC emissions are not underestimated in proportion to other ( mostly scattering) aerosol types. South Asia is the dominant contributor to sulfate aerosols over the INDOEX region and accounts for 60 - 70% of the AOD by sulfate. It is also an important but not the dominant contributor to carbonaceous aerosols over the INDOEX region with a contribution of less than 40% to the AOD by this aerosol species. The presence of elevated plumes brings significant quantities of aerosols to the Indian Ocean that are generated over Africa and Southeast and east Asia.

期刊论文 2004-08-20 DOI: 10.1029/2004JD004557 ISSN: 2169-897X
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