@article {castrillejo_comparability_2023,
	title = {Comparability of Radiocarbon Measurements in Dissolved Inorganic Carbon of Seawater Produced at ETH-Zurich},
	journal = {Radiocarbon},
	year = {2023},
	note = {Publisher: Cambridge University Press},
	month = {03/2023},
	pages = {1{\textendash}10},
	abstract = {Radiocarbon observations (Δ14C) in dissolved inorganic carbon (DIC) of seawater provide useful information about ocean carbon cycling and ocean circulation. To deliver high-quality observations, the Laboratory of Ion Beam Physics (LIP) at ETH-Zurich developed a new simplified method allowing the rapid analysis of radiocarbon in DIC of small seawater samples, which is continually assessed by following internal quality controls. However, a comparison with externally produced 14C measurements to better establish an equivalency between methods was still missing. Here, we make the first intercomparison with the National Ocean Sciences Accelerator Mass Spectrometry (NOSAMS) facility based on 14 duplicate seawater samples collected in 2020. We also compare with prior deep-water observations from the 1970s to 1990s. The results show a very good agreement in both comparisons. The mean Δ14C of 12 duplicate samples measured by LIP and NOSAMS were statistically identical within one sigma uncertainty while two other duplicate samples agreed within two sigma. Based on this small number of duplicate samples, LIP values appear to be slightly lower than the NOSAMS values, but more measurements will be needed for confirmation. We also comment on storage and preservation techniques used in this study, including the freezing of samples collected in foil bags.},
	keywords = {14C, comparison, DIC, dissolved inorganic carbon, radiocarbon, SEAWATER},
	issn = {0033-8222, 1945-5755},
	doi = {10.1017/RDC.2023.16},
	url = {https://www.cambridge.org/core/journals/radiocarbon/article/comparability-of-radiocarbon-measurements-in-dissolved-inorganic-carbon-of-seawater-produced-at-ethzurich/B9F6C6AA45835FA3ED0BF8E0CD9788E3},
	author = {Castrillejo, Maxi and Hansman, Roberta L. and Graven, Heather D. and Lester, Joanna G. and Bollhalder, Silvia and K{\"u}ndig, Kayley and Wacker, Lukas}
}
@article {2615,
	title = {Microbial decomposition of marine dissolved organic matter in cool oceanic crust},
	journal = {Nature Geoscience},
	volume = {11},
	year = {2018},
	month = {Jan-05-2018},
	pages = {334 - 339},
	abstract = {Marine dissolved organic carbon (DOC) is one of the largest active reservoirs of reduced carbon on Earth. In the deep ocean, DOC has been described as biologically recalcitrant and has a radiocarbon age of 4,000 to 6,000 years, which far exceeds the timescale of ocean overturning. However, abiotic removal mechanisms cannot account for the full magnitude of deep-ocean DOC loss. Deep-ocean water circulates at low temperatures through volcanic crust on ridge flanks, but little is known about the associated biogeochemical processes and carbon cycling.
Here we present analyses of DOC in fluids from two borehole observatories installed in crustal rocks west of the Mid-Atlantic Ridge, and show that deep-ocean DOC is removed from these cool circulating fluids. The removal mechanism is isotopically selective and causes a shift in specific features of molecular composition, consistent with microbe-mediated oxidation. We suggest organic molecules with an average radiocarbon age of 3,200 years are bioavailable to crustal microbes, and that this removal mechanism may account for at least 5\% of the global loss of DOC in the deep ocean. Cool crustal circulation probably contributes to maintaining the deep ocean as a reservoir of {\textquoteright}aged{\textquoteright} and refractory DOC by discharging the surviving organic carbon constituents that are molecularly degraded and depleted in C-14 and C-13 into the deep ocean.},
	keywords = {carbon, community, deep-ocean, DISTINCT, extraction, fluid-flow, HEAT, MID-ATLANTIC RIDGE, SEAWATER, WESTERN FLANK},
	issn = {1752-0894},
	doi = {10.1038/s41561-018-0109-5},
	url = {http://www.nature.com/articles/s41561-018-0109-5http://www.nature.com/articles/s41561-018-0109-5.pdfhttp://www.nature.com/articles/s41561-018-0109-5http://www.nature.com/articles/s41561-018-0109-5.pdf},
	author = {Shah Walter, Sunita R. and Jaekel, Ulrike and Osterholz, Helena and Fisher, Andrew T. and Huber, Julie A. and Pearson, Ann and Dittmar, Thorsten and Girguis, Peter R.}
}
@article {1284,
	title = { Allochthonous sources and dynamic cycling of ocean dissolved organic carbon revealed by carbon isotopes},
	journal = {GEOPHYSICAL RESEARCH LETTERS},
	volume = {44},
	year = {2017},
	month = {03/2017},
	pages = {2407-2415},
	abstract = {We present concentration and isotopic profiles of total, size, and polarity fractionated dissolved organic carbon (DOC) from Station ALOHA (A Long-term Oligotrophic Habitat Assessment), an oligotrophic site in the North Pacific Ocean. The data show that, between the surface and 3500 m, low molecular weight (LMW) hydrophilic DOC, LMW hydrophobic DOC, and high molecular weight (HMW) DOC constitute 22-33\%, 45-52\%, and 23-35\% of DOC, respectively. LMW hydrophilic DOC is more isotopically depleted (delta C-13 of -23.9 parts per thousand to -31.5 parts per thousand and Delta C-14 of -304 parts per thousand to -795 parts per thousand; mean age of 2850 to 15000 years) than the LMW hydrophobic DOC (delta C-13 of -22 parts per thousand to -23 parts per thousand and Delta C-14 of -270 parts per thousand to -568 parts per thousand; 2470 to 6680 years) and HMW DOC (delta C-13 of similar to-21 parts per thousand and Delta C-14 of -24 parts per thousand to -294 parts per thousand; 135-2700 years). Our analyses suggest that a large fraction of DOC may be derived from allochthonous sources such as terrestrial and hydrothermal DOC and cycle on much longer time scales of > 10000 years or enter the ocean as preaged carbon.},
	keywords = {ATLANTIC BIGHT, BLACK CARBON, C-14, HUMIC SUBSTANCES, MATTER, NORTH PACIFIC-OCEAN, RADIOCARBON ANALYSIS, SARGASSO SEA, SEAWATER, SPECTROMETRY},
	doi = {10.1002/2016GL071348},
	author = {Zigah, Prosper K. and McNichol, Ann P. and Xu, Li and Johnson, Carl and Santinelli, Chiara and Karl, David M. and Repeta, Daniel J.}
}
@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.}
}
@article {2094,
	title = {Precambrian marine carbonate isotope database: Version 1.1},
	journal = {Geochemistry Geophysics Geosystems},
	volume = {3},
	year = {2002},
	note = {561enTimes Cited:103
Cited References Count:26
},
	month = {Jun 6},
	pages = {1-12},
	abstract = {[1] We present a compilation of strontium, carbon, and oxygen isotope compositions of roughly 10,000 marine carbonate rocks of Archean - Ordovician age (3800 Ma - 450 Ma). The Precambrian Marine Carbonate Isotope Database (PMCID) has been compiled from 152 published and 3 unpublished articles and books of the past 40 years. Also included are 30 categories of relevant "metadata{\textquoteright}{\textquoteright} that allow detailed comparisons and quality assessments of the isotope data to be made. The PMCID will be updated periodically as new data and better age constraints come to light. Here we outline the structure of the first published version of the database and its inherent merits and limitations.},
	keywords = {1010 geochemistry : chemical evolution, 1030 geochemistry : geochemical cycles (0330), 1040 geochemistry : isotopic composition/chemistry, 1050 geochemistry : marine geochemistry (4835,4850), calcite, carbonates, cycle, dolomite, evolution, Geochemistry, isotope stratigraphy, oceans, precambrian, SEAWATER, sediments, strontium, sulfur, time},
	isbn = {1525-2027},
	doi = {10.1029/2001GC000266},
	author = {Shields, G. and Veizer, J.}
}
@article {2299,
	title = {An isotopic biogeochemical study of Neoproterozoic and Early Cambrian sediments from the Centralian Superbasin, Australia},
	journal = {Geochim Cosmochim Acta},
	volume = {61},
	year = {1997},
	note = {Logan, G ASummons, R E
Hayes, J M
eng
Research Support, U.S. Gov{\textquoteright}t, Non-P.H.S.
1997/01/01 00:00
Geochim Cosmochim Acta. 1997;61(24):5391-409.
},
	month = {1997},
	pages = {5391-409},
	abstract = {Organic matter from Neoproterozoic and Early Cambrian sediments of the Amadeus and Officer basins of the Centralian Superbasin, Australia, has been studied for biomarker distributions and the carbon isotopic compositions of kerogen and individual hydrocarbons. These sediments represent both shallow and deep water marine facies in the older sections and marine and saline lacustrine carbonate deposits in the Cambrian. Hydrocarbon biomarker patterns were found to be quite consistent with the known sedimentary environments and provide valuable insights into the biogeochemical changes which accompanied the transition from a microbially-dominated ocean to the early stages of metazoan radiation. In particular, carbon isotopic data for n-alkyl and isoprenoid lipids presented here, and in earlier studies, showed a reversal in carbon isotopic ordering between the Proterozoic and Phanerozoic. By comparison with the delta 13C of kerogen, n-alkyl lipids from deep-water Proterozoic sediments were enriched in 13C and appear to be derived mainly from heterotrophs whilst open marine Phanerozoic counterparts are 13C depleted and evidently derived mainly from autotrophs. Data from the samples studied here are consistent with a model invoking a change in the redox structure of the ocean, possibly aided by the innovation of faecal pellets.},
	keywords = {Alkanes/analysis/chemistry, Animals, australia, biomarkers, carbon isotopes, Carbon/analysis/*chemistry, Cyanobacteria, Eukaryota, Feces, Fossils, Geologic Sediments/*analysis/chemistry, Hydrocarbons/analysis, NASA Discipline Exobiology, Non-NASA Center, Paleontology, phytoplankton, SEAWATER, Terpenes/analysis, Zooplankton},
	isbn = {0016-7037 (Print)0016-7037 (Linking)
},
	url = {https://www.ncbi.nlm.nih.gov/pubmed/11540731},
	author = {Logan, G. A. and Summons, R. E. and Hayes, J. M.}
}
