@article {2675,
	title = {Biomass-Derived Provenance Dominates Glacial Surface Organic Carbon in the Western HimalayaBiomass-Derived Provenance Dominates Glacial Surface Organic Carbon in the Western Himalaya},
	journal = {Environmental Science \& Technology},
	volume = {54},
	year = {2020},
	month = {Sep-07-2021},
	pages = {8612 - 8621},
	abstract = {The origin, transport pathway, and spatial variability of total organic carbon (OC) in the western Himalayan glaciers are poorly understood compared to those of black carbon (BC) and dust, but it is critically important to evaluate the climatic role of OC in the region. By applying the distribution of OC activation energy; C-14 activity; and radiogenic isotopes of Pb-208/Pb-204, (207)pb/(204)pb and (206)pb/Pb-204 in glacial debris and atmospheric particulate matter (PM10 size fraction), we demonstrate that 98.3 +/- 1.6 and 1.7 +/- 1.6\% of OC in western Himalayan glaciers are derived from biomass and petrogenic sources, respectively. The (delta C-13 and N/C composition indicates that the biomass is a complex mixture of C3 vegetation and autochthonous photoautotrophic input modified by heterotrophic microbial activity. The data set reveals that the studied western Himalayan glacier has negligible contributions from fossil-fuel- derived particles, which contrasts to the central and eastern Himalayan glaciers that have significant contributions from fossil fuel sources. We show that this spatial variability of OC sources relates to regional differences in air mass transport pathways and precipitation regimes over the Himalaya. Moreover, our observation suggests that biomass-derived carbon could be the only primary driver of carbon-induced glacier melting in the western Himalaya.},
	keywords = {; MASS BALANCES, AEROSOLS, ALBEDO REDUCTION, ATMOSPHERIC LEAD, BLACK CARBON, DUST TRANSPOR, isotopic composition, PB, SNOW ALBEDO, TIBETAN PLATEAU},
	issn = {0013-936X},
	doi = {10.1021/acs.est.0c0271010.1021/acs.est.0c02710.s001},
	url = {https://apps.webofknowledge.com/InboundService.do?product=WOS\&Func=Frame\&DestFail=http\%3A\%2F\%2Fwww.webofknowledge.com\&SrcApp=search\&SrcAuth=Alerting\&SID=8Aqj2WiW4A71bymjSli\&customersID=Alerting\&mode=FullRecord\&IsProductCode=Yes\&AlertId=ab9062f8-b111-4f95-},
	author = {Nizam, Sarwar and Sen, Indra S. and Vinoj, Velu and Galy, Valier and Selby, David and Azam, Mohammad F. and Pandey, Satyendra K. and Creaser, Robert A. and Agarwal, Avinash K. and Singh, Akhilendra P. and Bizimis, Michael}
}
@article {2766,
	title = {Sources and radiocarbon ages of aerosol organic carbon along the east coast of China and implications for atmospheric fossil carbon contributions to China marginal seas},
	journal = {Science of The Total Environment},
	volume = {619-620},
	year = {2018},
	month = {Jan-04-2018},
	pages = {957 - 965},
	abstract = {Aerosol deposition is an important mechanism for the delivery of terrestrial organic carbon (OC) to marginal seas, but OC age characteristics of aerosols are not well constrained and their contributions to sediment OC burial have not been quantified. Total suspended particle samples were collected along the east coast of China at Changdao (CD), Qingdao (QD) and Huaniao Island (HNI), and were analyzed for total organic carbon (TOC) isotopes (13C and 14C) in order to bridge this information gap. TOC δ13C and Δ14C values ranged from - 23.6 to - 30.5{\textperthousand}, and - 153 to - 687{\textperthousand}, respectively, with the latter corresponding to 14C ages ranging from 1280 to 9260 yr. Estimated contributions of fossil carbon to TOC based on 14C mass balance approach ranged from 26 to 73\%, with strong seasonal variations in fossil carbon observed at CD. Fossil carbon at CD showed the highest proportion (73\%) in winter, reflecting anthropogenic emissions and the lowest proportion (26\%) in summer, caused by biomass contribution (annual ave., 52\% {\textpm} 17\%). In contrast, the fossil carbon at both QD (57{\textendash}64\%) and HNI (57{\textendash}67\%) dominated throughout the year, reflecting local anthropogenic influences and long-range transport. Mass balance estimates indicate that atmospheric deposition and riverine export accounted for 31\% and 69\% of fossil carbon inputs to the China marginal seas (CMS) respectively, with fossil carbon burial efficiencies approaching 100\% in the CMS. On a global scale, an atmospheric fossil carbon deposition flux of 17.2 Tg C yr- 1 was estimated, equivalent to 40\% of the estimated fluvial flux to the ocean, and potentially accounting for 24{\textendash}41\% of fossil OC burial in marine sediments. Therefore, the atmospheric deposition constitutes an important source of fossil carbon to marine sediments, and could play a key role in regional and global scale OC budgets and biogeochemical cycles.},
	keywords = {AEROSOLS, China marginal seas, Fossil carbon, Radiocarbon (14C) tracer, Total organic carbon},
	issn = {00489697},
	doi = {10.1016/j.scitotenv.2017.11.201},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S004896971733259X},
	author = {Yu, Meng and Guo, Zhigang and Wang, Xuchen and Eglinton, Timothy Ian and Yuan, Zineng and Xing, Lei and Zhang, Hailong and Zhao, Meixun}
}
