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Chen, SJ, Russell LM, Cappa CD, Zhang XL, Kleeman MJ, Kumar A, Liu D, Ramanathana V.  2019.  Comparing black and brown carbon absorption from AERONET and surface measurements at wintertime Fresno. Atmospheric Environment. 199:164-176.   10.1016/j.atmosenv.2018.11.032   AbstractWebsite

The radiative impacts of black carbon (BC) and brown carbon (BrC) are widely recognized but remain highly uncertain. The Aerosol Robotic Network (AERONET) provides measurements of aerosol optical depth (AOD), aerosol absorption optical depth (AAOD), and other parameters. AERONET AAOD measurements have been used to estimate the relative contributions of BC and BrC to the total absorption at select sites and have the potential to be used across the global network, but the accuracy of the partitioning method has not been established and the uncertainties not characterized. We made surface-level measurements of aerosol optical properties from January 13 to February 10, 2013, and from December 25, 2014, to January 13, 2015, at Fresno, California. The contribution of BrC and BC to the absorption at 405 nm was estimated from the surface-level measurements using a combined mass absorption coefficient and thermodenuder method. The surface-level measurements were compared with BC and BrC absorption at 440 nm estimated from AERONET measurements of the absolute AAOD and the absorption angstrom ngstrom exponent (AERONET-AAE method). In 2013, AERONET results showed that BC and BrC contributed 67% and 33%, respectively, of absorption at 440 nm while the surface-level measurements showed that BC and BrC contributed 89% and 11%, respectively, of absorption at 405 nm. In 2014, AERONET results showed BC and BrC absorption were 72% and 28%, respectively, and the BC and BrC surface measurements were 68% and 32%, respectively. The boundary layer conditions showed that the comparison between AERONET measurements and surface-based estimates was more appropriate in 2014 than in 2013. As a result, AERONET measurements and surface-based estimates had strong or moderate correlations and slopes near unity in 2014. Thus, surface measurements were more representative of column BC and BrC absorption in 2014.

Bosch, C, Andersson A, Kirillova EN, Budhavant K, Tiwari S, Praveen PS, Russell LM, Beres ND, Ramanathan V, Gustafsson O.  2014.  Source-diagnostic dual-isotope composition and optical properties of water-soluble organic carbon and elemental carbon in the South Asian outflow intercepted over the Indian Ocean. Journal of Geophysical Research-Atmospheres. 119:11743-11759.   10.1002/2014jd022127   AbstractWebsite

The dual carbon isotope signatures and optical properties of carbonaceous aerosols have been investigated simultaneously for the first time in the South Asian outflow during an intensive campaign at the Maldives Climate Observatory on Hanimaadhoo (MCOH) (February and March 2012). As one component of the Cloud Aerosol Radiative Forcing Dynamics Experiment, this paper reports on the sources and the atmospheric processing of elemental carbon (EC) and water-soluble organic carbon (WSOC) as examined by a dual carbon isotope approach. The radiocarbon (C-14) data show that WSOC has a significantly higher biomass/biogenic contribution (865%) compared to EC (594%). The more C-13-enriched signature of MCOH-WSOC (-20.80.7) compared to MCOH-EC (-25.8 +/- 0.3 parts per thousand) and megacity Delhi WSOC (-24.1 +/- 0.9 parts per thousand) suggests that WSOC is significantly more affected by aging during long-range transport than EC. The C-13-C-14 signal suggests that the wintertime WSOC intercepted over the Indian Ocean largely represents aged primary biomass burning aerosols. Since light-absorbing organic carbon aerosols (Brown Carbon (BrC)) have recently been identified as potential contributors to positive radiative forcing, optical properties of WSOC were also investigated. The mass absorption cross section of WSOC (MAC(365)) was 0.5 +/- 0.2 m(2)g(-1) which is lower than what has been observed at near-source sites, indicating a net decrease of WSOC light-absorption character during long-range transport. Near-surface WSOC at MCOH accounted for similar to 1% of the total direct solar absorbance relative to EC, which is lower than the BrC absorption inferred from solar spectral observations of ambient aerosols, suggesting that a significant portion of BrC might be included in the water-insoluble portion of organic aerosols.

Chung, CE, Ramanathan V, Decremer D.  2012.  Observationally constrained estimates of carbonaceous aerosol radiative forcing. Proceedings of the National Academy of Sciences of the United States of America. 109:11624-11629.   10.1073/pnas.1203707109   AbstractWebsite

Carbonaceous aerosols (CA) emitted by fossil and biomass fuels consist of black carbon (BC), a strong absorber of solar radiation, and organic matter (OM). OM scatters as well as absorbs solar radiation. The absorbing component of OM, which is ignored in most climate models, is referred to as brown carbon (BrC). Model estimates of the global CA radiative forcing range from 0 to 0.7 Wm(-2), to be compared with the Intergovernmental Panel on Climate Change's estimate for the pre-Industrial to the present net radiative forcing of about 1.6 Wm(-2). This study provides a model-independent, observationally based estimate of the CA direct radiative forcing. Ground-based aerosol network data is integrated with field data and satellite-based aerosol observations to provide a decadal (2001 through 2009) global view of the CA optical properties and direct radiative forcing. The estimated global CA direct radiative effect is about 0.75 Wm(-2) (0.5 to 1.0). This study identifies the global importance of BrC, which is shown to contribute about 20% to 550-nm CA solar absorption globally. Because of the inclusion of BrC, the net effect of OM is close to zero and the CA forcing is nearly equal to that of BC. The CA direct radiative forcing is estimated to be about 0.65 (0.5 to about 0.8) Wm(-2), thus comparable to or exceeding that by methane. Caused in part by BrC absorption, CAs have a net warming effect even over open biomass-burning regions in Africa and the Amazon.

Praveen, PS, Ahmed T, Kar A, Rehman IH, Ramanathan V.  2012.  Link between local scale BC emissions in the Indo-Gangetic Plains and large scale atmospheric solar absorption. Atmospheric Chemistry and Physics. 12:1173-1187.   10.5194/acp-12-1173-2012   AbstractWebsite

Project Surya has documented indoor and outdoor concentrations of black carbon (BC) from traditional biomass burning cook stoves in a rural village located in the Indo-Gangetic Plains (IGP) region of N. India from November 2009-September 2010. In this paper, we systematically document the link between local scale aerosol properties and column averaged regional aerosol optical properties and atmospheric radiative forcing. We document observations from the first phase of Project Surya and estimate the source dependent (biomass and fossil fuels) aerosol optical properties from local to regional scale. Data were collected using surface based observations of BC, organic carbon (OC), aerosol light absorption, scattering coefficient at the Surya village (SVI_1) located in IGP region and integrated with satellite and AERONET observations at the regional scale (IGP). The daily mean BC concentrations at SVI_1 showed a large increase of BC during the dry season (December to February) with values reaching 35 mu g m(-3). Space based LIDAR data revealed how the biomass smoke was trapped within the first kilometer during the dry season and extended to above 5 km during the pre-monsoon season. As a result, during the dry season, the variance in the daily mean single scattering albedo (SSA), the ratio of scattering to extinction coefficient, and column aerosol optical properties at the local IGP site correlated (with slopes in the range of 0.85 to 1.06 and R-2 > 0.4) well with the "IGP_AERONET" (mean of six AERONET sites). The statistically significant correlation suggested that in-situ observations can be used to derive spatial mean forcing, at least for the dry season. The atmospheric forcing due to BC and OC exceeded 20 Wm(-2) during all months from November to May, supporting the deduction that elimination of cook stove smoke emissions through clean cooking technologies will likely have a major positive impact not only on human health but also on regional climate.