@article {liu_pre-aged_2023,
	title = {Pre-aged terrigenous organic carbon biases ocean ventilation-age reconstructions in the North Atlantic},
	journal = {Nature Communications},
	volume = {14},
	number = {1},
	year = {2023},
	note = {Number: 1 Publisher: Nature Publishing Group},
	month = {06/2023},
	abstract = {Changes in ocean ventilation have been pivotal in regulating carbon sequestration and release on centennial to millennial timescales. However, paleoceanographic reconstructions documenting changes in deep-ocean ventilation using 14C dating, may bear multidimensional explanations, obfuscating the roles of ocean ventilation played on climate evolution. Here, we show that previously inferred poorly ventilated conditions in the North Atlantic were linked to enhanced pre-aged organic carbon (OC) input during Heinrich Stadial 1 (HS1). The 14C age of sedimentary OC was approximately 13,345 {\textpm} 692 years older than the coeval foraminifera in the central North Atlantic during HS1, which is coupled to a ventilation age of 5,169 {\textpm} 660 years. Old OC was mainly of terrigenous origin and exported to the North Atlantic by ice-rafting. Remineralization of old terrigenous OC in the ocean may have contributed to, at least in part, the anomalously old ventilation ages reported for the high-latitude North Atlantic during HS1.},
	keywords = {Carbon cycle, Marine chemistry, Palaeoceanography},
	issn = {2041-1723},
	doi = {10.1038/s41467-023-39490-6},
	url = {https://www.nature.com/articles/s41467-023-39490-6},
	author = {Liu, Jingyu and Wang, Yipeng and Jaccard, Samuel L. and Wang, Nan and Gong, Xun and Fang, Nianqiao and Bao, Rui}
}
@article {2923,
	title = {Carbon Isotopic and Lithologic Constraints on the Sources and Cycling of Inorganic Carbon in Four Large Rivers in China: Yangtze, Yellow, Pearl, and Heilongjiang},
	journal = {Journal of Geophysical Research: Biogeosciences},
	volume = {126},
	year = {2021},
	month = {Jan-02-2021},
	abstract = {Transport of terrigenous carbon by rivers has been affected extensively by climate change and anthropogenic activities in China over the last few decades. Here, we present results on carbon isotopes (C-13, C-14) of dissolved and particulate inorganic carbon (DIC and PIC) and combined with major lithologic ions measured in the four largest rivers in China, namely, the Yangtze, Yellow, Pearl, and Heilongjiang rivers, to reveal the sources and transport of terrigenous inorganic carbon in the rivers. The DIC concentrations showed large variations in the four rivers and ranged from 253 to 3,122 mu M. The Yangtze, Yellow and Pearl rivers transported high DIC contents that had low Delta C-14 values of millennium-aged DIC and very old PIC; however, the Heilongjiang River presented a lower DIC concentration with much younger C-14 ages than the global average (1,100 mu M). The strong correlations between the DIC isotope values and major lithological ions (Ca2+ and Mg2+) suggest that chemical weathering played important but variable roles in controlling the production and fate of DIC in the rivers. Using dual isotopes and the MixSIAR model, we calculated that the chemical weathering of carbonate rocks contributed 95 +/- 5\% of the riverine DIC to the headwater of the Yangtze River while silicate rock weathering and riverine organic matter respiration contributed 62 +/- 25\% and 5 +/- 5\% of the DIC in the middle and lower reaches of the river, respectively. In contrast, chemical weathering of silicate rocks contributed the dominant fraction of DIC in the Yellow (55 +/- 17\%), Pearl (61 +/- 20\%) and Heilongjiang (83 +/- 29\%) rivers.},
	keywords = {Carbon cycle, Chemical weathering, inorganic carbon in large rivers, radiocarbon, stable carbon isotope},
	issn = {2169-8953},
	doi = {10.1029/2020JG005901},
	url = {https://apps.webofknowledge.com/InboundService.do?product=WOS\&Func=Frame\&DestFail=http\%3A\%2F\%2Fwww.webofknowledge.com\&SrcApp=search\&SrcAuth=Alerting\&SID=7EQ3XpZtZiWye3DFos4\&customersID=Alerting\&mode=FullRecord\&IsProductCode=Yes\&AlertId=4d48b20a-7d27-4fa2-},
	author = {Shan, Sen and Luo, Chunle and Qi, Yuanzhi and Cai, Wei-Jun and Sun, Shuwen and Fan, Di and Wang, Xuchen}
}
@article {2921,
	title = {Climate control on terrestrial biospheric carbon turnover},
	journal = {Proceedings of the National Academy of Sciences},
	volume = {118},
	year = {2021},
	month = {Nov-02-2022},
	pages = {e2011585118},
	abstract = {Terrestrial vegetation and soils hold three times more carbon than the atmosphere. Much debate concerns how anthropogenic activity will perturb these surface reservoirs, potentially exacerbating ongoing changes to the climate system. Uncertainties specifically persist in extrapolating point-source observations to ecosystem-scale budgets and fluxes, which require consideration of vertical and lateral processes on multiple temporal and spatial scales. To explore controls on organic carbon (OC) turnover at the river basin scale, we present radiocarbon (C-14) ages on two groups of molecular tracers of plant-derived carbon-leaf-wax lipids and lignin phenols-from a globally distributed suite of rivers. We find significant negative relationships between the C-14 age of these biomarkers and mean annual temperature and precipitation. Moreover, riverine biospheric-carbon ages scale proportionally with basin-wide soil carbon turnover times and soil C-14 ages, implicating OC cycling within soils as a primary control on exported biomarker ages and revealing a broad distribution of soil OC reactivities. The ubiquitous occurrence of a long-lived soil OC pool suggests soil OC is globally vulnerable to perturbations by future temperature and precipitation increase. Scaling of riverine biospheric-carbon ages with soil OC turnover shows the former can constrain the sensitivity of carbon dynamics to environmental controls on broad spatial scales. Extracting this information from fluvially dominated sedimentary sequences may inform past variations in soil OC turnover in response to anthropogenic and/or climate perturbations. In turn, monitoring riverine OC composition may help detect future climate-change-induced perturbations of soil OC turnover and stocks.},
	keywords = {Carbon cycle, carbon turnover times, fluvial carbon, plant biomarkers, radiocarbon},
	issn = {0027-8424},
	doi = {10.1073/pnas.2011585118},
	url = {https://www.researchgate.net/publication/349357864_Climate_control_on_terrestrial_biospheric_carbon_turnover},
	author = {Eglinton, Timothy I. and Galy, Valier V. and Hemingway, Jordon D. and Feng, Xiaojuan and Bao, Hongyan and Blattmann, Thomas M. and Dickens, Angela F. and Gies, Hannah and Giosan, Liviu and Haghipour, Negar and Hou, Pengfei and Lupker, Maarten and McIntyre, Cameron P. and Montlu{\c c}on, Daniel B. and Peucker-Ehrenbrink, Bernhard and Ponton, Camilo and Schefu{\ss}, Enno and Schwab, Melissa S. and Voss, Britta M. and Wacker, Lukas and Wu, Ying and Zhao, Meixun}
}
@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 {2636,
	title = {Using Stable Carbon Isotopes to Quantify Radiocarbon Reservoir Age Offsets in the Coastal Black SeaAbstract},
	journal = {Radiocarbon},
	volume = {61},
	year = {2019},
	month = {Jan-02-2019},
	pages = {309 - 318},
	abstract = {Constraining radiocarbon (C-14) reservoir age offsets is critical to deriving accurate calendar-age chronologies from C-14 dating of materials which did not draw carbon directly from the atmosphere. The application of C-14 dating to such materials is severely limited in hydrologically sensitive environments like the Black Sea because of the difficulty to quantify reservoir age offsets, which can vary quickly and significantly through time, due to the dynamics of the biogeochemical cycling of carbon. Here we reconstruct C-14 reservoir age offsets (Rshell-atm) of Holocene bivalve shells from the coastal Black Sea relatively to their contemporaneous atmosphere. We show that the C-14 reservoir age offset and the stable carbon isotope composition of bivalve shells are linearly correlated in this region. From a biogeochemical standpoint, this suggests that inorganic stable carbon isotope and C-14 compositions of Black Sea coastal waters are controlled by the balance between autochthonous primary productivity and heterotrophic respiration of allochthonous pre-aged terrestrial organic matter supplied by rivers. This provided an important implication for Black Sea geochronology as the reservoir age offset of C-14-dated bivalve shell can be inferred from its stable carbon isotope composition. Our results provide a fundamental and inexpensive geochemical tool which will considerably improve the accuracy of Holocene calendar age chronologies in the Black Sea.},
	keywords = {Black Sea, Carbon cycle, freshwater reservoir effect, Geochronology, Reservoir age},
	issn = {0033-8222},
	doi = {10.1017/RDC.2018.61},
	url = {https://www.cambridge.org/core/product/identifier/S0033822218000619/type/journal_articlehttps://www.cambridge.org/core/services/aop-cambridge-core/content/view/S0033822218000619},
	author = {Soulet, Guillaume and Giosan, Liviu and Flaux, Cl{\'e}ment and Galy, Valier}
}
@article {2840,
	title = {Aged dissolved organic carbon exported from rivers of the Tibetan Plateau},
	journal = {PLOS ONE},
	volume = {12},
	year = {2017},
	month = {Feb-05-2019},
	pages = {e0178166},
	abstract = {The role played by river networks in regional and global carbon cycle is receiving increasing attention. Despite the potential of radiocarbon measurements (14C) to elucidate sources and cycling of different riverine carbon pools, there remain large regions such as the climate-sensitive Tibetan Plateau for which no data are available. Here we provide new 14C data on dissolved organic carbon (DOC) from three large Asian rivers (the Yellow, Yangtze and Yarlung Tsangpo Rivers) running on the Tibetan Plateau and present the carbon transportation pattern in rivers of the plateau versus other river system in the world. Despite higher discharge rates during the high flow season, the DOC yield of Tibetan Plateau rivers (0.41 gC m-2 yr-1) was lower than most other rivers due to lower concentrations. Radiocarbon ages of the DOC were older/more depleted (511{\textpm}294 years before present, yr BP) in the Tibetan rivers than those in Arctic and tropical rivers. A positive correlation between radiocarbon age and permafrost watershed coverage was observed, indicating that 14C-deplted/old carbon is exported from permafrost regions of the Tibetan Plateau during periods of high flow. This is in sharp contrast to permafrost regions of the Arctic which export 14C-enriched carbon during high discharge periods.},
	keywords = {Carbon cycle, Carbon dioxide, Climate change, Rain, Rivers, Surface water, Tibetan people, TIBETAN PLATEAU},
	doi = {10.1371/journal.pone.0178166},
	url = {https://dx.plos.org/10.1371/journal.pone.0178166},
	author = {Qu, Bin and Sillanp{\"a}{\"a}, Mika and Li, Chaoliu and Kang, Shichang and Stubbins, Aron and Yan, Fangping and Aho, Kelly Sue and Zhou, Feng and Raymond, Peter A.},
	editor = {Lin, Senjie}
}
@article {2487,
	title = {Methane emissions proportional to permafrost carbon thawed in Arctic lakes since the 1950s},
	journal = {Nature Geoscience},
	volume = {9},
	year = {2016},
	month = {Oct-08-2017},
	pages = {679 - 682},
	abstract = {Permafrost thaw exposes previously frozen soil organic matter to microbial decomposition. This process generates methane and carbon dioxide, and thereby fuels a positive feedback process that leads to further warming and thaw1. Despite widespread permafrost degradation during the past ~40 years2, 3, 4, the degree to which permafrost thaw may be contributing to a feedback between warming and thaw in recent decades is not well understood. Radiocarbon evidence of modern emissions of ancient permafrost carbon is also sparse5. Here we combine radiocarbon dating of lake bubble trace-gas methane (113 measurements) and soil organic carbon (289 measurements) for lakes in Alaska, Canada, Sweden and Siberia with numerical modelling of thaw and remote sensing of thermokarst shore expansion. Methane emissions from thermokarst areas of lakes that have expanded over the past 60 years were directly proportional to the mass of soil carbon inputs to the lakes from the erosion of thawing permafrost. Radiocarbon dating indicates that methane age from lakes is nearly identical to the age of permafrost soil carbon thawing around them. Based on this evidence of landscape-scale permafrost carbon feedback, we estimate that 0.2 to 2.5 Pg permafrost carbon was released as methane and carbon dioxide in thermokarst expansion zones of pan-Arctic lakes during the past 60 years.},
	keywords = {Carbon cycle, Climate change, Cryospheric science},
	issn = {1752-0894},
	doi = {10.1038/ngeo2795},
	url = {http://www.nature.com/doifinder/10.1038/ngeo2795},
	author = {Walter Anthony, Katey and Daanen, Ronald and Anthony, Peter and Schneider von Deimling, Thomas and Ping, Chien-Lu and Chanton, Jeffrey P. and Grosse, Guido}
}
@article {2638,
	title = {Hidden cycle of dissolved organic carbon in the deep ocean},
	journal = {Proceedings of the National Academy of Sciences},
	volume = {111},
	year = {2014},
	month = {Jan-11-2016},
	pages = {16706 - 16711},
	abstract = {Marine dissolved organic carbon (DOC) is a large (660 Pg C) reactive carbon reservoir that mediates the oceanic microbial food web and interacts with climate on both short and long timescales. Carbon isotopic content provides information on the DOC source via [Formula: see text]C and age via [Formula: see text]C. Bulk isotope measurements suggest a microbially sourced DOC reservoir with two distinct components of differing radiocarbon age. However, such measurements cannot determine internal dynamics and fluxes. Here we analyze serial oxidation experiments to quantify the isotopic diversity of DOC at an oligotrophic site in the central Pacific Ocean. Our results show diversity in both stable and radio isotopes at all depths, confirming DOC cycling hidden within bulk analyses. We confirm the presence of isotopically enriched, modern DOC cocycling with an isotopically depleted older fraction in the upper ocean. However, our results show that up to 30\% of the deep DOC reservoir is modern and supported by a 1 Pg/y carbon flux, which is 10 times higher than inferred from bulk isotope measurements. Isotopically depleted material turns over at an apparent time scale of 30,000 y, which is far slower than indicated by bulk isotope measurements. These results are consistent with global DOC measurements and explain both the fluctuations in deep DOC concentration and the anomalous radiocarbon values of DOC in the Southern Ocean. Collectively these results provide an unprecedented view of the ways in which DOC moves through the marine carbon cycle.},
	keywords = {Carbon cycle, carbon isotopes, dissolved organic carbon, Oceanography, radiocarbon},
	issn = {0027-8424},
	doi = {10.1073/pnas.1407445111},
	url = {http://www.pnas.org/lookup/doi/10.1073/pnas.1407445111https://syndication.highwire.org/content/doi/10.1073/pnas.1407445111},
	author = {Follett, Christopher L. and Repeta, Daniel J. and Rothman, Daniel H. and Xu, Li and Santinelli, Chiara}
}
@article { ISI:000290199000003,
	title = {Multiple-source heterotrophy fueled by aged organic carbon in an urbanized estuary},
	journal = {MARINE CHEMISTRY},
	volume = {124},
	number = {{1-4}},
	year = {2011},
	month = {MAR 20},
	pages = {14-22},
	type = {Article},
	abstract = {The lower Hudson River is a highly urbanized estuary that receives large inputs of treated wastewater. To determine how organic matter from wastewater influences carbon cycling in this type of system, we measured chlorophyll a, pCO(2). dissolved organic carbon (DOC), delta(13)C-DOC, and Delta(14)C-DOC along the salinity gradient and at wastewater treatment plants. Isotopic mixing curves indicate a net removal of DOC that is (13)C enriched and (14)C depleted. The amount of DOC removed was consistent with CO(2) evasion from the estuary. During two transects at average to low flow, the lower Hudson River Estuary was a heterotrophic system with CO(2) evasion balanced by the utilization of aged DOC derived from wastewater and marine phytoplankton that enter the estuary at the seaward end-member. DOC removals were largest during a period of high river flow, when isotopic mixing curves also suggest large contributions from labile terrestrial OC sources. Overall, our results suggest that net heterotrophy in the lower Hudson River Estuary is fueled by aged labile DOC derived from a combination of sources, which are influenced by seasonal phytoplankton blooms, hydrological conditions, and the nature of wastewater inputs. (C) 2010 Elsevier B.V. All rights reserved.},
	keywords = {(13)C, (14)C, Carbon cycle, Carbon dioxide, Chlorophyll, dissolved organic carbon, Heterotrophy, Hudson River Estuary, Isotope mixing curves, Sewage, USA, Wastewater},
	issn = {0304-4203},
	doi = {10.1016/j.marchem.2010.11.003},
	author = {Griffith, David R. and Raymond, Peter A.}
}
@article {2096,
	title = {Inorganic carbon in the Indian Ocean: Distribution and dissolution processes},
	journal = {Global Biogeochemical Cycles},
	volume = {16},
	year = {2002},
	note = {643rkTimes Cited:50
Cited References Count:72
},
	month = {Oct-Nov},
	abstract = {This study uses nearly 25,000 carbon measurements from the WOCE/JGOFS global CO2 survey to examine the distribution of dissolved inorganic carbon (DIC) and total alkalinity (TA) in the Indian Ocean. Shallow and intermediate distributions of inorganic carbon do not strictly follow temperature and salinity because of differing surface gradients and vertical biological processes that work to modify the circulation derived features. Anthropogenic CO2 has increased the shallow DIC by as much as 3\%, decreasing the vertical DIC gradient. Deep ocean DIC and TA increase toward the north because of the decomposition and dissolution of organic and inorganic particles. Calcite saturation depths range from 2900-3900 m with the deepest saturation depth in the central Indian Ocean. Variations of aragonite saturation depth (200-1400 m) are similar to calcite, but the deepest saturations are in the southwestern Indian Ocean. The shallowest aragonite saturation depths are found in the Bay of Bengal. In the northern Arabian Sea and Bay of Bengal, the current aragonite saturations are 100 and 200 m shallower, respectively, than in preindustrial times. Estimates of carbonate dissolution rates on isopycnal surfaces range from 0.017 to 0.083 mumol kg(-1) yr(-1) in deep waters. Upper water column dissolution rates range from 0 to 0.73 mumol kg(-1) yr(-1), with a local maximum occurring in intermediate waters just below the aragonite saturation horizon. Dissolution is also generally higher north of the Chemical Front at 10-20degreesS. There is some evidence for significant sedimentary sources in the northern Indian Ocean.},
	keywords = {alkalinity, anthropogenic co2, arabian sea, calcium carbonate, Carbon cycle, dioxide system, dissociation, indian ocean, pressure, saturation state, SEAWATER, Temperature, thermodynamics, total alkalinity, total co2, water},
	isbn = {0886-6236},
	doi = {10.1029/2002GB001869},
	author = {Sabine, C. L. and Key, R. M. and Feely, R. A. and Greeley, D.}
}
