An ammonia-oxidizing, carbon-fixing archaeon, Candidatus ''Nitrosopumilus maritimus,'' recently was isolated from a salt-water aquarium, definitively confirming that chemoautotrophy exists among the marine archaea. However, in other incubation studies, pelagic archaea also were capable of using organic carbon. It has remained unknown what fraction of the total marine archaeal community is autotrophic in situ. If archaea live primarily as autotrophs in the natural environment, a large ammonia-oxidizing population would play a significant role in marine nitrification. Here we use the natural distribution of radiocarbon in archaeal membrane lipids to quantify the bulk carbon metabolism of archaea at two depths in the subtropical North Pacific gyre. Our compound-specific radiocarbon data show that the archaea in surface waters incorporate modern carbon into their membrane lipids, and archaea at 670 m incorporate carbon that is slightly more isotopically enriched than inorganic carbon at the same depth. An isotopic mass balance model shows that the dominant metabolism at depth indeed is autotrophy (83%), whereas heterotrophic consumption of modern organic carbon accounts for the remainder of archaeal biomass. These results reflect the in situ production of the total community that produces tetraether lipids and are not subject to biases associated with incubation and͞or culture experiments. The data suggest either that the marine archaeal community includes both autotrophs and heterotrophs or is a single population with a uniformly mixotrophic metabolism. The metabolic and phylogenetic diversity of the marine archaea warrants further exploration; these organisms may play a major role in the marine cycles of nitrogen and carbon.biomarkers ͉ carbon isotopes ͉ microbial ecology ͉ nitrogen cycle ͉ oceanography N onthermophilic archaea represent up to 40% of the free-living prokaryotic community in the water column of the world's oceans (1-6), but until recently there has been limited information about the sources of carbon and energy that fuel these organisms (7-11). The characteristic membrane lipids of planktonic archaea include glycerol dialkyl glycerol tetraethers (GDGTs) (12). These compounds are ubiquitous in marine sediments and ocean water (12-15). The relative abundance of individual GDGTs recovered from sediments is used to reconstruct sea-surface temperatures (16)(17)(18). This distribution, known as TEX 86 , has been shown through experimental manipulation of surface-water mesocosm experiments to respond to changes in incubation temperature (18). In addition, the ␦ 13 C values of GDGTs display a remarkably constant offset from ␦ 13 C values of dissolved inorganic carbon (DIC) over a range of settings and geologic time (13,(19)(20)(21). The collective metabolic activities of the numerous archaea in the ocean are likely to play a significant role in the cycling of organic carbon (OC) and nutrients, and their membrane lipids show significant utility for paleoceanography. However, neither the metabolic requiremen...

We have developed techniques for accurately and precisely measuring samples containing less than a few hundred micrograms of carbon, using a compact AMS system (NEC 0.5 MV 1.5SDH-1). Detailed discussions of the sample preparation, measurement setup, data analysis and background corrections for a variety of standard samples ranging from 0.002 to 1 mgC are reported. Multiple aliquots of small amounts of CO 2 were reduced to graphite with H 2 over pre-baked iron powder catalyst. A reduction reaction temperature of 450°C was adopted for graphite samples below 0.05 mgC, rather than the usual 550°C used on samples of 0.1-1 mgC. In our regular reactors ($3.1 cm 3 ), this reduction in temperature improved the graphite yield from $60 to 90-100% for samples ranging from 0.006-0.02 mgC. The combination of lower reaction temperature with a reduced reactor volume ($1.6 cm 3 ) gave yields as high as 100% on graphite samples <0.006 mgC. High performance measurements on ultra-small samples are possible also due to a modified NEC MC-SNIC ion-source that generates C À currents of 1 lA per lg of carbon for samples in the 0.002 to 0.010 mgC range, combined with on-line measurement of 12 C and 13 C (AMS d 13 C) to correct machine-induced isotopic fractionation. Source efficiencies are in excess of 10%, which enables 4-5% of the radiocarbon atoms in 0.005-0.010 mgC samples to be measured. Examination of the background samples revealed two components: (a) 0.2-1 lg of modern carbon and (b) 0.1-0.5 lg of dead carbon. The latter component can be ignored when measuring unknown samples paired to small standards of precisely identical size (matching size normalizing standard method). Otherwise, one must make corrections for both background components. Ultra-small samples from 0.002 to 0.01 mgC can be measured with accuracy and precision of a few percent, based on scatter in results for multiple aliquots of a primary standard and deviations of secondary standards from their known values.

This paper presents a compilation of atmospheric radiocarbon for the period 1950–2019, derived from atmospheric CO2 sampling and tree rings from clean-air sites. Following the approach taken by Hua et al. (2013), our revised and extended compilation consists of zonal, hemispheric and global radiocarbon (14C) data sets, with monthly data sets for 5 zones (Northern Hemisphere zones 1, 2, and 3, and Southern Hemisphere zones 3 and 1–2). Our new compilation includes smooth curves for zonal data sets that are more suitable for dating applications than the previous approach based on simple averaging. Our new radiocarbon dataset is intended to help facilitate the use of atmospheric bomb 14C in carbon cycle studies and to accommodate increasing demand for accurate dating of recent (post-1950) terrestrial samples.

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