@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 { ISI:000280946500002,
	title = {In situ cosmogenic Be-10 production-rate calibration from the Southern Alps, New Zealand},
	journal = {QUATERNARY GEOCHRONOLOGY},
	volume = {5},
	number = {{4}},
	year = {2010},
	month = {AUG},
	pages = {392-409},
	type = {Article},
	abstract = {We present a Be-10 production-rate calibration derived from an early Holocene debris-flow deposit at about 1000 m above sea level in the central Southern Alps, New Zealand, in the mid-latitude Southern Hemisphere. Ten radiocarbon ages on macrofossils from a soil horizon buried by the deposit date the deposit to 9690 +/- 50 calendar years before AD2008. Surface Be-10 concentrations of seven large boulders partially embedded in the stable surface of the deposit are tightly distributed, yielding a standard deviation of similar to 2\%. Conversion of the Be-10 measurements to sea level/high-latitude values using each of five standard scaling methods indicates Be-10 production rates of 3.84 +/- 0.08, 3.87 +/- 0.08, 3.83 +/- 0.08, 4.15 +/- 0.09, and 3.74 +/- 0.08 atoms g(-1) a(-1), relative to the {\textquoteleft}07KNSTD{\textquoteright} Be-10 AMS standard, and including only the local time-integrated production-rate uncertainties. When including a sea level high-latitude scaling uncertainty the overall error is similar to 2.5\% (1 sigma) for each rate. To test the regional applicability of this production-rate calibration, we measured Be-10 concentrations in a set of nearby moraines deposited before 18060 +/- 200 years before AD2008. The Be-10 ages are only consistent with minimum-limiting C-14 age data when calculated using the new production rates. This also suggests that terrestrial in situ cosmogenic-nuclide production did not change significantly from Last Glacial Maximum to Holocene time in New Zealand. Our production rates agree well with those of a recent calibration study from northeastern North America, but are 12-14\% lower than other commonly adopted values. The production-rate values presented here can be used elsewhere in New Zealand for rock surfaces exposed during or since the last glacial period. (C) 2009 Elsevier B.V. All rights reserved.},
	keywords = {Be-10, C-14, Cosmogenic nuclide, Debris flow, Holocene, Last glacial maximum, Moraine, Production rate, South Island},
	issn = {1871-1014},
	doi = {10.1016/j.quageo.2009.12.001},
	author = {Putnam, A. E. and Schaefer, J. M. and Barrell, D. J. A. and Vandergoes, M. and Denton, G. H. and Kaplan, M. R. and Finkel, R. C. and Schwartz, R. and Goehring, B. M. and Kelley, S. E.}
}
@article {2446,
	title = {Method for determining coal carbon in the reclaimed minesoils contaminated with coal},
	journal = {Soil Science Society of America Journal},
	volume = {72},
	year = {2008},
	note = {24},
	month = {Jan-Feb},
	pages = {231-237},
	abstract = {Minesoils are anthropic soils developed on land disturbed by mining activities. Minesoils developed on the reclaimed surface-mined sites for coal are contaminated with coal particles resulting from mining and reclamation activities. Therefore, the total organic carbon (TOC) pool in these sites is a mixture of coal and plant-derived recent soil organic carbon (SOC). Accurate estimates of SOC pools and C sequestration rates in the reclaimed minesoils (RMS) is limited by the lack of a standard and cost-effective method for determination of coal C concentrations in the RMS. The chemi-thermal method, based on the oxidative resistance of coal, was developed and validated with radiocarbon analysis using selected artificial soil-coal mixtures and minesoil samples. Radiocarbon analysis of RMS samples indicated that minesoils from the top 10-cm depth developing from topsoil applied during reclamation was coal C free. The contribution of coal C and the radiocarbon age of TOC increased with increasing soil depth. The coal C fraction accounted for 0 to 92\% of TOC in the RMS samples. The coal C fraction was highly correlated with delta C-13 (r(2) = 0.84), suggesting that stable isotope composition could estimate the coal C concentration in RMS samples. Analysis of coal and artificial soil and coal mixtures indicated that chemi-thermal treatment was effective in removing recent SOC with minimum effect on coal. Analysis of RMS samples indicated that both radiocarbon activity and the chemi-thermal method were effective in estimating coal C concentration in RMS of southeast Ohio. The coal C concentrations for both methods were highly correlated (r(2) = 0.95), suggesting that the chemi-thermal method was as effective as radiocarbon activity measurement in estimating coal C concentration in these soils.},
	keywords = {BLACK CARBON, C-14, FOREST, GENESIS, MATTER, MINING DISTRICT, RICH MINE SOILS, sediments, SITES, SOIL ORGANIC-CARBON},
	isbn = {0361-5995},
	doi = {10.1016/j.dsr2.2008.07.005},
	author = {Ussiri, D. A. N. and Lai, R.}
}
@conference {1802,
	title = {Taphonomy and ages of bivalve shells from San Salvador Island, Bahamas},
	volume = {40},
	year = {2008},
	note = {id: 2219; Source type: conferencepapers\&proceedings; Object type: Article; Object type: Conference Paper; Copyright: GeoRef, Copyright 2008, American Geological Institute. Reference includes data supplied by the Geological Society of America, Boulder, CO, United States; CSAUnique: 2010-024085; AccNum: 2010-024085; ISSN: 0016-7592; CODEN: GAAPBC},
	month = {2008},
	pages = {230},
	publisher = {Geological Society of America (GSA), Boulder, CO, United States (USA)},
	organization = {Geological Society of America (GSA), Boulder, CO, United States (USA)},
	address = {United States (USA)},
	abstract = {Paleontological interpretations of taphonomic processes can be complimented by examining abrasion and age of shells in modern settings. A preliminary analysis of the ages of bivalves from Haitian Boat Beach (just east of Barkers Point, northwest coast of San Salvador Island, Bahamas) provides a range of ages of shell material exposed on modern beaches of San Salvador Island and provides estimates of the timing of beach rock lithification. At Haitian Boat Beach Beach, bivalves and gastropods were collected from shell accumulations preserved on the beach as well as within a single 3 to 5-cm thick horizon of beach rock. The ages of 2 valves (Genus Chione) from the beach and 4 valves (Genus Chione and Genus Glycymeris) from the beach rock were analyzed. Two of the most abraded shells were selected for analysis from the beach in an attempt to get a maximum age of beach shell material. These shells were radiocarbon dated by measuring carbon-14 at NOSAMS and converted to calendar years using the CALIB program of Stuiver and Reimer (1993). Two abraded valves collected from the beach yielded calendar year ages BP of 512 and 549 years. The beach rock valves yielded calendar year ages BP of 143, 129, and 1628. These results suggest lithification of beach rock was initiated},
	keywords = {10, abrasion, absolute age, Bahamas, beachrock, Bivalvia, C-14, carbon, carbonate rocks, Caribbean region, Cenozoic, Chione, dates, Gastropoda, Glycymeris, Heterodonta, Holocene, interpretation, Invertebrata, Invertebrate paleontology, isotopes, lithification, living taxa, Mollusca, Quaternary, radioactive isotopes, San Salvador, sedimentary rocks, sediments, shells, taphonomy, upper Holocene, Veneridae, Veneroida, West Indies},
	author = {Pruss, Sara B.}
}
@article {2444,
	title = {A study of secondary organic aerosol formation in the anthropogenic-influenced southeastern United States},
	journal = {Journal of Geophysical Research-Atmospheres},
	volume = {112},
	year = {2007},
	note = {263D13302
},
	month = {Jul},
	abstract = {[1] The formation of secondary organic aerosol (SOA) in an anthropogenic-influenced region in the southeastern United States is investigated by a comparison with urban plumes in the northeast. The analysis is based on measurements of fine-particle organic compounds soluble in water (WSOC) as a measure of secondary organic aerosol. Aircraft measurements over a large area of northern Georgia, including the Atlanta metropolitan region, and in plumes from New York City and surrounding urban regions in the northeast show that fine-particle WSOC are spatially correlated with vehicle emission tracers (e.g., CO), yet the measurements indicate that vehicles do not directly emit significant particulate WSOC. In addition to being correlated, WSOC concentrations were in similar proportions to anthropogenic tracers in both regions, despite biogenic volatile organic compounds (VOCs) that were on average 10-100 times higher over northern Georgia. In contrast, radiocarbon analysis on WSOC extracted from integrated filters deployed in Atlanta suggests that roughly 70-80\% of the carbon in summertime WSOC is modern. If both findings are valid, the combined results indicate that in northern Georgia, fine-particle WSOC was secondary and formed through a process that involves mainly modern biogenic VOCs but which is strongly linked to an anthropogenic component that may largely control the mass of SOA formed. Independent of the radiocarbon results, a strong association between SOA and anthropogenic sources has implications for control strategies in urban regions with large biogenic VOC emissions.},
	keywords = {AMBIENT AEROSOL, atmosphere, C-14, emissions, evolution, GASOLINE, OXIDATION, PARTICLES, RATIOS, ZURICH},
	isbn = {2169-897X},
	doi = {10.1029/2007JD008408},
	author = {Weber, R. J. and Sullivan, A. P. and Peltier, R. E. and Russell, A. and Yan, B. and Zheng, M. and de Gouw, J. and Warneke, C. and Brock, C. and Holloway, J. S. and Atlas, E. L. and Edgerton, E.}
}
@article {2003,
	title = {Input of particulate organic and dissolved inorganic carbon from the Amazon to the Atlantic Ocean},
	journal = {Geochemistry Geophysics Geosystems},
	volume = {6},
	year = {2005},
	note = {909pwTimes Cited:17
Cited References Count:21
},
	month = {Mar 18},
	abstract = {We report concentrations and isotope measurements (radiocarbon and stable carbon) of dissolved inorganic carbon (DIC) and suspended particulate organic carbon (POC) in waters collected from the mouth of the Amazon River and the North Brazil Current. Samples were collected in November 1991, when the Amazon hydrograph was at its annual minimum and the North Brazil Current had retroflected into the equatorial North Atlantic. The DIC D 14 C results revealed postbomb carbon in river and ocean waters, with slightly higher values at the river mouth. The low DIC delta(13)C signature of the river end-member (-11\%) demonstrates that about half of the DIC originated from the remineralization of terrestrially derived organic matter. A linear relationship between DIC and salinity indicates that DIC was mixed nearly conservatively in the transition zone from the river mouth to the open ocean, though there was a small amount (<= 10\%) of organic matter remineralization in the mesohaline region. The POC Delta(14)C values in the river mouth were markedly lower than those values from the western Amazon region (Hedges et al., 1986). We conclude that the dominant source of POC near the river mouth and in the inner Amazon plume during November 1991 was aged, resuspended material of significant terrestrial character derived from shelf sediments, while the outer plume contained mainly marine-derived POC.},
	keywords = {accumulation, amazon, C-14, carbon cycling, CO2, continental-shelf, poc, radiocarbon, river system, Sediment, total co(2), water},
	isbn = {1525-2027},
	doi = {10.1029/2004GC000842},
	author = {Druffel, E. R. M. and Bauer, J. E. and Griffin, S.}
}
@article {2083,
	title = {Penetration of anthropogenic carbon into organic particles of the deep ocean},
	journal = {Geophysical Research Letters},
	volume = {30},
	year = {2003},
	note = {709dpTimes Cited:12
Cited References Count:29
},
	month = {Jul 23},
	pages = {1744},
	abstract = {[1] In the late 1980s, bomb C-14 was present in suspended particulate organic carbon (POC) from the North Central Pacific (NCP) and Sargasso Sea ( SS) throughout most of the water column, demonstrating that deep POC had exchanged with atmospheric CO2 in the past 30 years. Upon reoccupation of these sites in 1999 and 2000, respectively, we observed that the delta(13)C values of suspended POC were lower than those measured a decade earlier. This demonstrates that anthropogenic CO2 from fossil fuel and biomass burning has penetrated a major organic matter pool in the deep ocean. Delta(14)C measured in the suspended POC showed similar or higher values in the deep Sargasso Sea and decreased values in the deep NCP compared to those measured previously. We use a box model to show that the differences in the radiocarbon results are likely due to the presence of resuspended sediment that is laterally advected from the continental margin to the deep Sargasso Sea.},
	keywords = {bomb radiocarbon, C-14, CO2, delta-c-13, MATTER, NORTH PACIFIC-OCEAN, SARGASSO SEA, Sediment, variability, water},
	isbn = {0094-8276},
	doi = {10.1029/2003GL017423},
	author = {Druffel, E. R. M. and Bauer, J. E. and Griffin, S. and Hwang, J.}
}
@article {2436,
	title = {Installation of a 134-sample MC-SNICS ion source at NOSAMS and first results},
	journal = {Nuclear Instruments \& Methods in Physics Research Section B-Beam Interactions with Materials and Atoms},
	volume = {172},
	year = {2000},
	note = {8th International Conference on Accelerator Mass SpectrometrySEP 06-10, 1999
VIENNA, AUSTRIA
},
	month = {Oct},
	pages = {247-251},
	abstract = {In April 1999, the National Ocean Sciences AMS (NOSAMS) facility received the shipment of a 134-sample MC-SNICS ion source from the National Electrostatics Corporation (NEC). It replaced one of the two 59-sample spherical ionizer sources (US-AMS Model 3090A, HVEE Model 846). In this paper, we will describe the adaptation of the NEC ion source to the US-AMS/HVEE recombinator injector at NOSAMS. This is the first lime that the two leading sputter ion source designs are directly comparable on the same system. We will present ion beam optics calculations for both in comparison with measured results. Once fully operational, the new ion source will assume all of the sputter sample measurements at NOSAMS, while the remaining 59-sample source will be replaced by the newly developed microwave gas ion source. One of the most desirable features of the MC-SNICS design is the smaller cathode geometry. At comparable extracted currents, the surface diameter of the pressed samples is reduced from 1.5 to 1 mm. A new, automatic sample pressing procedure is being developed for this design. This will improve the capability for preparing and analyzing smaller sputter samples (carbon weight <100 <mu>g). Our US-AMS cathodes showed considerable reduction in the extracted currents when the sample diameter was reduced to 1 mm, even with samples of normal size (>200 mug C). (C) 2000 Elsevier Science B.V. All rights reserved.},
	keywords = {AMS, beam extraction/injection, C-14, ion sources, ocean, pacific},
	isbn = {0168-583X},
	author = {von Reden, K. F. and Bellino, M. and Long, P. and Schneider, R. J. and Loger, R.}
}
@conference {1692,
	title = {Microscale AMS (super <sup>14</sup>) C measurement at NOSAMS},
	volume = {40},
	year = {1998},
	note = {id: 2237; Source type: conferencepapers\&proceedings; Object type: Article; Object type: Conference Paper; Copyright: GeoRef, Copyright 2007, American Geological Institute.; CSAUnique: 1999-044438; AccNum: 1999-044438; ISSN: 0033-8222; CODEN: RACAAT},
	month = {1998},
	pages = {61-75},
	publisher = {University of Arizona, Department of Geosciences, Tucson, AZ, United States (USA)},
	organization = {University of Arizona, Department of Geosciences, Tucson, AZ, United States (USA)},
	address = {United States (USA)},
	abstract = {Techniques for making precise and accurate radiocarbon accelerator mass spectrometry (AMS) measurements on samples containing less than a few hundred micrograms of carbon are being developed at the NOSAMS facility. A detailed examination of all aspects of the sample preparation and data analysis process shows encouraging results. Small quantities of CO (sub 2) are reduced to graphite over cobalt catalyst at an optimal temperature of 605 degrees C. Measured (super 14) C/ (super 12) C ratios of the resulting targets are affected by machine-induced isotopic fractionation, which appears directly related to the decrease in ion current generated by the smaller sample sizes. It is possible to compensate effectively for this fractionation by measuring samples relative to small standards of identical size. Examination of the various potential sources of background (super 14) C contamination indicates that the sample combustion process is the largest contributor, adding ca. 1 mu g of carbon with a less-than-modern (super 14) C concentration.},
	keywords = {03, absolute age, accelerator mass spectroscopy, accuracy, C-14, C-14/C-12, carbon, Carbon dioxide, combustion, data processing, Geochronology, graphite, isotope fractionation, isotopes, mass spectroscopy, mathematical methods, methods, native elements, radioactive isotopes, sample preparation, size, spectroscopy, Stable isotopes},
	doi = {10.1017/S0033822200017902},
	url = {http://hdl.handle.net/10150/653650},
	author = {Pearson, Ann and McNichol, Ann P. and Schneider, Robert J. and von Reden, Karl F. and Zheng, Yan}
}
@conference {1800,
	title = {(super 14) C AMS measurements of},
	volume = {40},
	year = {1998},
	note = {id: 2239; Source type: conferencepapers\&proceedings; Object type: Article; Object type: Conference Paper; Copyright: GeoRef, Copyright 2007, American Geological Institute.; CSAUnique: 1999-044459; AccNum: 1999-044459; ISSN: 0033-8222; CODEN: RACAAT},
	month = {1998},
	pages = {247-253},
	publisher = {University of Arizona, Department of Geosciences, Tucson, AZ, United States (USA)},
	organization = {University of Arizona, Department of Geosciences, Tucson, AZ, United States (USA)},
	address = {United States (USA)},
	abstract = {The NOSAMS facility at Woods Hole Oceanographic Institution has started to develop and apply techniques for measuring very small samples on a standard Tandetron accelerator mass spectrometry (AMS) system with high-current hemispherical Cs sputter ion sources. Over the past year, results on samples ranging from 7 to 160 mu g C showed both the feasibility of such analyses and the present limitations on reducing the size of solid carbon samples. One of the main factors affecting the AMS results is the dependence of a number of the beam optics parameters on the extracted ion beam current. The extracted currents range from 0.5 to 10 mu A of (super 12) C (super -) for the sample sizes given above. We here discuss the setup of the AMS system and methods for reliable small-sample measurements and give the AMS-related limits to sample size and the measurement uncertainties.},
	keywords = {03, absolute age, accelerator mass spectroscopy, C-14, carbon, dilution, Geochronology, ions, isotopes, mass spectroscopy, precision, radioactive isotopes, sample preparation, spectroscopy, volume},
	author = {von Reden, Karl F. and McNichol, Ann P. and Pearson, Ann and Schneider, Robert J.}
}
@article {2340,
	title = {Post-bomb radiocarbon records of surface corals from the tropical Atlantic Ocean},
	journal = {Radiocarbon},
	volume = {38},
	year = {1996},
	note = {Xd080Times Cited:25
Cited References Count:20
},
	month = {1996},
	pages = {563-572},
	abstract = {Delta(14)C records are reported for post-bomb corals from three sites in the tropical Atlantic Ocean. In corals from 18 degrees S in the Brazil Current, Delta(14)C values increased from ca.-58 parts per thousand in the early 1950s to +138 parts per thousand by 1974, then decreased to 110 parts per thousand by 1982 Shorter records from 8 degrees S off Brazil and from the Cape Verde Islands (17 degrees N) showed initially higher Delta(14)C values before 1965 than those at 18 degrees S, but showed lower rates of increase of Delta(14)C during the early 1960s. There is general agreement between the coral results and Delta(14)C of dissolved inorganic carbon (DIC) measured in seawater previously for locations in the tropical Atlantic Ocean. Delta(14)C values at our tropical ocean sites increased at a slower rate than those observed previously in the temperate North Atlantic (Florida and Bermuda), owing to the latter{\textquoteright}s proximity to the bomb C-14 input source in the northern hemisphere. Model results show that from 1960-1980 the Cape Verde coral and selected DIC Delta(14)C values from the North Equatorial Current agree with that calculated for the North Atlantic based on an isopycnal mixing model with a constant water mass renewal rate between surface and subsurface waters. This is in contrast to Delta(14)C values in Bermuda corals that showed higher post-bomb values than those predicted using a constant water mass renewal rate, hence indicating that ventilation in the western north Atlantic Ocean had decreased by a factor of 3 during the 1960s and 1970s (Druffel 1989).},
	keywords = {atmosphere, banded corals, bermuda, C-14, pacific, rings, ventilation},
	isbn = {0033-8222},
	author = {Druffel, E. R. M.}
}
@conference {1758,
	title = {Progress of the NOSAMS facility WOCE (super 14) C data analysis},
	volume = {38},
	year = {1996},
	note = {id: 2242; Source type: conferencepapers\&proceedings; Object type: Article; Object type: Conference Paper; Copyright: GeoRef, Copyright 2007, American Geological Institute.; CSAUnique: 1999-071631; AccNum: 1999-071631; ISSN: 0033-8222; CODEN: RACAAT},
	month = {1996},
	pages = {123},
	publisher = {University of Arizona, Department of Geosciences, Tucson, AZ, United States (USA)},
	organization = {University of Arizona, Department of Geosciences, Tucson, AZ, United States (USA)},
	address = {United States (USA)},
	keywords = {02D, 07, accelerator mass spectroscopy, C-14, carbon, Isotope geochemistry, isotopes, mass spectroscopy, Oceanography, Pacific Ocean, progress report, radioactive isotopes, report, sea water, spectroscopy},
	author = {von Reden, K. F. and McNichol, A. P. and Schneider, Robert J.}
}
@conference {1794,
	title = {Stable and radio-carbon isotope measurements in the Pacific Ocean; contributions from NOSAMS},
	volume = {77},
	year = {1996},
	note = {id: 2240; Source type: conferencepapers\&proceedings; Object type: Article; Object type: Conference Paper; Copyright: GeoRef, Copyright 2007, American Geological Institute.; CSAUnique: 1997-047916; AccNum: 1997-047916; ISSN: 0096-3941; CODEN: EOSTAJ},
	month = {1996},
	pages = {79},
	publisher = {American Geophysical Union, Washington, DC, United States (USA)},
	organization = {American Geophysical Union, Washington, DC, United States (USA)},
	address = {United States (USA)},
	keywords = {02D, 07, accelerator mass spectroscopy, C-13/C-12, C-14, carbon, chemical analysis, geochemical indicators, high-resolution methods, Isotope geochemistry, isotope ratios, isotopes, marine geology, mass spectroscopy, National Ocean Sciences Accelerator Mass Spectrometry, NOSAMS, Oceanography, Pacific Ocean, radioactive isotopes, radioactive tracers, sampling, sea water, spectroscopy, Stable isotopes, tracers, Woods Hole Oceanographic Institution},
	author = {McNichol, A. P. and von Reden, K. F. and Schneider, R. J. and Key, R. M. and Jones, G. A.}
}
@article {2369,
	title = {The Rapid Preparation of Seawater Sigma-Co2 for Radiocarbon Analysis at the National Ocean Sciences Ams Facility},
	journal = {Radiocarbon},
	volume = {36},
	year = {1994},
	note = {Pz926Times Cited:61
Cited References Count:14
},
	month = {1994},
	pages = {237-246},
	abstract = {We have established a laboratory for extracting Sigma CO2 from seawater samples for AMS analysis of the radiocarbon content. The seawater samples are collected at sea, poisoned and stored until analysis in the laboratory. Each sample is acidified; the inorganic carbon is stripped out as CO2 with an inert carrier gas and then converted to graphite. We present results for Buzzards Bay surface H2O and Na2CO3 standards that demonstrate we strip > 98\% of inorganic carbon from seawater. Stable isotope analyses are performed to better than 0.2 parts per thousand, and the reproducibility of C-14 measurements on Buzzards Bay seawater is better than 13 parts per thousand. Finally, we compare data from samples collected in 1991 to those collected in the 1970s and to large volume samples.},
	keywords = {accelerator mass-spectrometry, C-14, samples},
	isbn = {0033-8222},
	author = {McNichol, A. P. and Jones, G. A. and Hutton, D. L. and Gagnon, A. R. and Key, R. M.}
}
