@article {2661,
	title = {On the Origin of Aged Sedimentary Organic Matter Along a River-Shelf-Deep Ocean Transect},
	journal = {Journal of Geophysical Research: Biogeosciences},
	volume = {124},
	year = {2019},
	month = {Jun-08-2021},
	pages = {2582 - 2594},
	abstract = {To assess the influences of carbon sources and transport processes on the C-14 age of organic matter (OM) in continental margin sediments, we examined a suite of samples collected along a river-shelf-deep ocean transect in the East China Sea (ECS). Ramped pyrolysis-oxidiation was conducted on suspended particulate matter in the Yangtze River and on surface sediments from the ECS shelf and northern Okinawa Trough. C-14 ages were determined on OM decomposition products within different temperature windows. These measurements suggest that extensive amounts of pre-old (i.e., millennial age) organic carbon (OC) are subject to degradation within and beyond the Yangtze River Delta, and this process is accompanied by an exchange of terrestrial and marine OM. These results, combined with fatty acid concentration data, suggest that both the nature and extent of OM preservation/degradation as well as the modes of transport influence the C-14 ages of sedimentary OM. Additionally, we find that the age of (thermally) refractory OC increases during across-shelf transport and that the age offset between the lowest and highest temperature OC decomposition fractions also increases along the shelf-to-trough transect. Amplified interfraction spread or C-14 heterogeneity is the greatest in the Okinawa Trough. Aged sedimentary OM across the transect may be a consequence of several reasons including fossil OC input, selective degradation of younger OC, hydrodynamic sorting processes, and aging during lateral transport. Consequently, each of them should be considered in assessing the C-14 results of sedimentary OM and its implications for the carbon cycle and interpretation of sedimentary records.},
	keywords = {Carbon cycle, hydrodynamic processes, organic carbon, radiocarbon, sediments},
	issn = {2169-8953},
	doi = {10.1029/2019JG005107},
	url = { https://doi.org/10.1029/2019JG005107},
	author = {Bao, Rui and Zhao, Meixun and McNichol, Ann and Wu, Ying and Guo, Xinyu and Haghipour, Negar and Eglinton, Timothy I.}
}
@article {2641,
	title = {Petrocarbon evolution: Ramped pyrolysis/oxidation and isotopic studies of contaminated oil sediments from the Deepwater Horizon oil spill in the Gulf of Mexico},
	journal = {PLOS ONE},
	volume = {14},
	year = {2019},
	month = {Apr-02-2021},
	pages = {e0212433},
	abstract = {Hydrocarbons released during the Deepwater Horizon (DWH) oil spill weathered due to exposure to oxygen, light, and microbes. During weathering, the hydrocarbons{\textquoteright} reactivity and lability was altered, but it remained identifiable as "petrocarbon" due to its retention of the distinctive isotope signatures (C-14 and C-13) of petroleum. Relative to the initial estimates of the quantity of oil-residue deposited in Gulf sediments based on 2010-2011 data, the overall coverage and quantity of the fossil carbon on the seafloor has been attenuated. To analyze recovery of oil contaminated deep-sea sediments in the northern Gulf of Mexico we tracked the carbon isotopic composition (C-13 and C-14, radiocarbon) of bulk sedimentary organic carbon through time at 4 sites. Using ramped pyrolysis/oxidation, we determined the thermochemical stability of sediment organic matter at 5 sites, two of these in time series. There were clear differences between crude oil (which decomposed at a lower temperature during ramped oxidation), natural hydrocarbon seep sediment (decomposing at a higher temperature; Delta C-14 = -189 parts per thousand) and our control site (decomposing at a moderate temperature; Delta C-14 = -189 parts per thousand), in both the stability (ability to withstand ramped temperatures in oxic conditions) and carbon isotope signatures. We observed recovery toward our control site bulk Delta C-14 composition at sites further from the wellhead in similar to 4 years, whereas sites in closer proximity had longer recovery times. The thermographs also indicated temporal changes in the composition of contaminated sediment, with shifts towards higher temperature CO2 evolution over time at a site near the wellhead, and loss of higher temperature CO2 peaks at a more distant site.},
	keywords = {C-14 ANALYSES; MARINE SNOW, degradation, fractionation, organic-matter, POLYCYCLIC AROMATIC-HYDROCARBONS; MICROBIAL COMMUNITY RESPONSE, radiocarbon, STABLE CARBON, surface sediments},
	doi = {10.1371/journal.pone.0212433},
	url = {https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0212433},
	author = {Rogers, Kelsey L. and Bosman, Samantha H. and Lardie-Gaylord, Mary and McNichol, Ann and Rosenheim, Brad E. and Montoya, Joseph P. and Chanton, Jeffrey P.},
	editor = {Cooper, Lee W.}
}
@article {2600,
	title = {Turning up the Heat on Organic Matter to Track Carbon},
	journal = {Eos},
	volume = {98},
	year = {2017},
	month = {Jul-09-2018},
	keywords = {Antarctic sediments, Foraminifera, radiocarbon, stable carbon isotopes},
	doi = {10.1029/2017EO080771},
	url = {https://eos.org/meeting-reports/turning-up-the-heat-on-organic-matter-to-track-carbon},
	author = {McNichol, Ann and Rosenheim, Brad and Galy, Valier}
}
