@article {2667,
	title = {Sources and radiocarbon ages of organic carbon in different grain size fractions of Yellow River-transported particles and coastal sediments},
	journal = {Chemical Geology},
	volume = {534},
	year = {2020},
	month = {Jan-02-2020},
	pages = {119452},
	keywords = {organic matter, RadiocarbonStable carbon isotope, Sediment grain size, Yellow River},
	issn = {00092541},
	doi = {10.1016/j.chemgeo.2019.119452},
	url = {https://www.sciencedirect.com/science/article/pii/S0009254119305819},
	author = {Ge, Tiantian and Xue, Yuejun and Jiang, Xueyan and Zou, Li and Wang, Xuchen}
}
@article {2642,
	title = {Temporal constraints on lateral organic matter transport along a coastal mud belt},
	journal = {Organic Geochemistry},
	volume = {128},
	year = {2019},
	month = {Jan-02-2019},
	pages = {86 - 93},
	abstract = {Constraints on timescales of lateral transport of sedimentary organic carbon (OC) over continental shelves and associated influences on the distribution and abundance of OC remain sparse. Preferential degradation of labile, young OC during lateral transport results in apparent {\textquotedblleft}diagenetic aging{\textquotedblright} of OC. Additionally, sediment translocation can also result in {\textquotedblleft}transport time-associated aging{\textquotedblright} of associated organic matter (OM) as a function of the lateral transport time (LTT). Here, we use a coupled thermal decomposition and radiocarbon (14C) approach to constrain timescales of lateral transport and concomitant loss of OC associated with different grain size fractions of sediments collected from two locations \~{}275 km apart along a dispersal pathway on the inner shelf of the East China Sea. The 14C age contrasts between corresponding thermal fractions are used to distinguish these two components of sedimentary OM {\textquotedblleft}aging{\textquotedblright}. To minimize interferences from hydrodynamic sorting and diagenetic aging of OC accompanying lateral transport, we assess 14C age differences of decomposition products from the most thermally-refractory OC components associated with specific grain size fractions between locations. We show that LTTs vary among different grain size fractions, and examine relationships between LTTs and sedimentary OC loss in order to assess the decomposition of OC as a consequence of lateral transport. We suggest that the decomposition of OC associated with protracted lateral transport exerts a strong influence on OC burial efficiency, with broad implications for carbon cycling over continental shelves.},
	keywords = {14C aging, Continental shelf seas, East China Sea, Mud belt, organic matter, Sediment resuspension},
	issn = {01466380},
	doi = {10.1016/j.orggeochem.2019.01.007},
	url = {https://www.sciencedirect.com/science/article/pii/S0146638019300075},
	author = {Bao, Rui and Zhao, Meixun and McNichol, Ann and Galy, Valier and McIntyre, Cameron and Haghipour, Negar and Eglinton, Timothy I.}
}
@article {2867,
	title = {Seasonal variability in the source and composition of particulate matter in the depositional zone of Baltimore Canyon, U.S. Mid-Atlantic Bight},
	journal = {Deep Sea Research Part I: Oceanographic Research Papers},
	volume = {127},
	year = {2017},
	month = {Jan-09-2017},
	pages = {77 - 89},
	abstract = {Submarine canyons are often hotspots of biomass due to enhanced productivity and funneling of organic matter of marine and terrestrial origin. However, most deep-sea canyons remain poorly studied in terms of their role as conduits of terrestrial and marine particles. A multi-tracer geochemical investigation of particles collected yearlong by a sediment trap in Baltimore Canyon on the US Mid-Atlantic Bight (MAB) revealed temporal variability in source, transport, and fate of particulate matter. Both organic biomarker composition (sterol and n-alkanes) and bulk characteristics (δ13C, Δ14C, Chl-a) suggest that while on average the annual contribution of terrestrial and marine organic matter sources are similar, 42\% and 52\% respectively, marine sources dominate. Elevated Chlorophyll-a and sterol concentrations during the spring sampling period highlight a seasonal influx of relatively fresh phytodetritus. In addition, the contemporaneous increase in the particle reactive micronutrients cadmium (Cd) and molybdenum (Mo) in the spring suggest increased scavenging, aggregation, and sinking of phytodetrital biomass in response to enhanced surface production within the nutricline. While tidally driven currents within the canyon resuspend sediment between 200 and 600 m, resulting in the formation of a nepheloid layer rich in lithogenic material, near-bed sediment remobilization in the canyon depositional zone was minimal. Instead, vertical transport and lateral transport across the continental margin were the dominant processes driving seasonal input of particulate matter. In turn, seasonal variability in deposited particulate organic matter is likely linked to benthic faunal composition and ecosystem scale carbon cycling.},
	keywords = {Deep-sea ecosystems, Geochemical analyses, organic matter, sediment trap, Submarine canyons},
	issn = {09670637},
	doi = {10.1016/j.dsr.2017.08.004},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0967063717300602},
	author = {Prouty, N.G. and Mienis, F. and Campbell-Swarzenski, P. and Roark, E.B. and Davies, A.J. and Robertson, C.M. and Duineveld, G. and Ross, S.W. and Rhode, M. and Demopoulos, A.W.J.}
}
@article { ISI:000337285500012,
	title = {Organic matter transformation in the peat column at Marcell Experimental Forest: Humification and vertical stratification},
	journal = {JOURNAL OF GEOPHYSICAL RESEARCH-BIOGEOSCIENCES},
	volume = {119},
	number = {{4}},
	year = {2014},
	month = {APR 28},
	pages = {661-675},
	type = {Article},
	abstract = {We characterized peat decomposition at the Marcell Experimental Forest (MEF), Minnesota, USA, to a depth of 2m to ascertain the underlying chemical changes using Fourier transform infrared (FT IR) and C-13 nuclear magnetic resonance (NMR) spectroscopy) and related these changes to decomposition proxies C:N ratio, C-13 and N-15, bulk density, and water content. FT IR determined that peat humification increased rapidly between 30 and 75cm, indicating a highly reactive intermediate-depth zone consistent with changes in C:N ratio, C-13 and N-15, bulk density, and water content. Peat decomposition at the MEF, especially in the intermediate-depth zone, is mainly characterized by preferential utilization of O-alkyl-C, carboxyl-C, and other oxygenated functionalities with a concomitant increase in the abundance of alkyl- and nitrogen-containing compounds. Below 75cm, less change was observed but aromatic functionalities and lignin accumulated with depth. Significant correlations with humification indices, identified by FT IR spectroscopy, were found for C:N ratios. Incubation studies at 22 degrees C revealed the highest methane production rates, greatest CH4:CO2 production ratios, and significant O-alkyl-C utilization within this 30 and 75cm zone. Oxygen-containing functionalities, especially O-alkyl-C, appear to serve as excellent proxies for soil decomposition rate and should be a sensitive indicator of the response of the solid phase peat to increased temperatures caused by climate change and the field study manipulations that are planned to occur at this site. Radiocarbon signatures of microbial respiration products in deeper pore waters at the MEF resembled the signatures of more modern dissolved organic carbon rather than solid phase peat, indicating that recently photosynthesized organic matter fueled the bulk of subsurface microbial respiration. These results indicate that carbon cycling at depth at the MEF is not isolated from surface processes.},
	keywords = {FT-IR spectroscopy, humification, NMR spectroscopy, organic matter, peatlands, vertical stratification},
	issn = {2169-8953},
	doi = {10.1002/2013JG002492},
	author = {Tfaily, Malak M. and Cooper, William T. and Kostka, Joel E. and Chanton, Patrick R. and Schadt, Christopher W. and Hanson, Paul J. and Iversen, Colleen M. and Chanton, Jeffrey P.}
}
@article {2460,
	title = {Seasonal variability of organic matter composition in an Alaskan glacier outflow: insights into glacier carbon sources},
	journal = {Environmental Research Letters},
	volume = {9},
	year = {2014},
	month = {Jan-05-2014},
	pages = {055005},
	abstract = {Glacier ecosystems are a significant source of bioavailable, yet ancient dissolved organic carbon
(DOC). Characterizing DOC in Mendenhall Glacier out flow (southeast Alaska) we document a
seasonal persistence to the radiocarbon-depleted signature of DOC, highlighting ancient DOC as
a ubiquitous feature of glacier out flow. We observed no systematic depletion in Δ14C-DOC with
increasing discharge during the melt season that would suggest mobilization of an aged subglacial carbon store. However, DOC concentration, δ13C-DOC,Δ14C-DOC and fluorescence signatures appear to have been in fluenced by runoff from vegetated hillslopes above the glacier during onset and senescence of melt. In the peak glacier melt period, the Δ 14 C-DOC of stream samples at the out flow (-181.7 to-355.3{\textperthousand}) was comparable to the Δ 14 C-DOC for snow samples from the accumulation zone (-207.2 to-390.9{\textperthousand}), suggesting that ancient DOC from the glacier surface is exported in glacier runoff. The pre-aged DOC in glacier snow and runoff is consistent with contributions from fossil fuel combustion sources similar to those documented previously in ice cores and thus provides evidence for anthropogenic perturbation of the carbon cycle. Overall, our results emphasize the need to further characterize DOC inputs to glacier ecosystems, particularly in light of predicted changes in glacier mass and runoff in the coming century.},
	keywords = {alaska, dissolved organic carbon, glacier, organic matter, radiocarbon},
	doi = {10.1088/1748-9326/9/5/055005},
	url = {http://iopscience.iop.org/article/10.1088/1748-9326/9/5/055005/meta},
	author = {Spencer, Robert G M and Vermilyea, Andrew and Fellman, Jason and Raymond, Peter and Stubbins, Aron and Scott, Durelle and Hood, Eran}
}
@conference {1278,
	title = {The Effect of Different Acid Treatments on the Radiocarbon Age of Sedimentary Organic Matter},
	booktitle = {EOS, Transactions, American Geophysical Union},
	year = {2001},
	note = {Date revised - 2007-02-01SuppNotes - Session: OS41A 9 The Truth About Paleoceanographic Proxies - What Are They Really Telling Us III Posters.Last updated - 2016-05-27},
	month = {January 2001},
	publisher = {American Geophysical Union, 2000 Florida Ave., N.W. Washington DC 20009 USA, [mailto:service@agu.org]},
	organization = {American Geophysical Union, 2000 Florida Ave., N.W. Washington DC 20009 USA, [mailto:service@agu.org]},
	abstract = {To date the bulk organic carbon in marine sediments it is necessary to first remove any inorganic carbon present by acidification. We tested three different acid treatments to see how the different methods affected the stable and radio-carbon isotopic values of the remaining organic matter. The standard NOSAMS method is to react the sediment with repeated aliquots of1.2N HCl until no visible dissolution reaction is present. The remaining sediment is then rinsed with distilled water. This method leaves a carbonate-free sediment that is easy to combust but suffers from the possible removal of acid-soluble organic matter. We compared this method to two methods that do not require rinsing of the sediments after acid treatment--a vapor phase acidification method using concentrated HCl (Hedges and Stern, 1984) and an in situ acidification with sulfurous acid (Verardo et al., 1990). Scaling these methods up to deal with the amount of sediment required for a radiocarbon date can present challenges that are not evident when dealing with the small quantities required for a percent organic carbon measurement. Vapor phase acidification of high carbonate sediments leaves hygroscopic salts that can impede sample combustion. Sulfurous acid is a weak acid and it is very difficult to determine when all the carbonate has been removed from a sediment sample. We tested sediments from 6 locations in (or near) the Atlantic Ocean that represented riverine, estuarine, and marine environments as well as a range of both organic and inorganic concentrations. We will present the isotopic results for these sediments and evaluate what is the most appropriate method to use. Hedges J.I. and J.H. Stern (1984) Limnol. Oceanogr. 29, 657-663. Verardo D.J., P.N. Froelich and A. McIntyre (1990) Deep-Sea Res. 37, 157-165.},
	keywords = {A, Atlantic, Acidification, Brackish, Brackishwater environment, carbon cycling, Chronostratigraphy, Estuarine sedimentation, organic carbon, organic matter, Palaeoceanography, Radioactivity and radioisotopes, Radiocarbon dating, Sediment chemistry, Stable isotopes},
	url = {https://search.proquest.com/docview/19468089?accountid=29119},
	author = {Batista, F and McNichol, A P and Gerlach, D S}
}
