This work summarizes the methodical capabilities, improvements, and new developments in the radiocarbon laboratory of the accelerator mass spectrometry (AMS) facility at the University of Cologne, Germany, which was established in 2010. During the past years, the laboratory has specialized in the analysis of small and gaseous samples. We thus, recently installed a second ion source dedicated for radiocarbon (14C) analysis of CO2 samples at our 6 MV Tandetron AMS from High Voltage Engineering Europe B.V. that is coupled with the gas injection system from Ionplus and an EuroVector EA 3000 elemental analyzer. This work summarizes all pretreatment methods and analytical facilities established in our laboratory during the last years including 14C analysis of individual organic compounds and of CO2 trapped on molecular sieves. We also report different blank values including our long-term blank since 2011, which is for normal-sized, solid samples (650–1000 µg C) 0.0012 ± 0.0004 F14C (54,305 ± 2581 yr BP, n = 484). The precision obtained for modern samples measured as graphite is 0.5% and for gaseous samples injected with the GIS ≤2%.

The release of greenhouse gases from the large organic carbon stock in permafrost deposits in the circumarctic regions may accelerate global warming upon thaw. The extent of this positive climate feedback is thought to be largely controlled by the microbial degradability of the organic matter preserved in these sediments. In addition, weathering and oxidation processes may release inorganic carbon preserved in permafrost sediments as CO2, which is generally not accounted for. We used 13C and 14C analysis and isotopic mass balances to differentiate and quantify organic and inorganic carbon released as CO2 in the field from an active retrogressive thaw slump of Pleistocene-age Yedoma and during a 1.5-years incubation experiment. The results reveal that the dominant source of the CO2 released from freshly thawed Yedoma exposed as thaw mound is Pleistocene-age organic matter (48–80%) and to a lesser extent modern organic substrate (3–34%). A significant portion of the CO2 originated from inorganic carbon in the Yedoma (17–26%). The mixing of young, active layer material with Yedoma at a site on the slump floor led to the preferential mineralization of this young organic carbon source. Admixtures of younger organic substrates in the Yedoma thaw mound were small and thus rapidly consumed as shown by lower contributions to the CO2 produced during few weeks of aerobic incubation at 4°C corresponding to approximately one thaw season. Future CO2 fluxes from the freshly thawed Yedoma will contain higher proportions of ancient inorganic (22%) and organic carbon (61–78%) as suggested by the results at the end, after 1.5 years of incubation. The increasing contribution of inorganic carbon during the incubation is favored by the accumulation of organic acids from microbial organic matter degradation resulting in lower pH values and, in consequence, in inorganic carbon dissolution. Because part of the inorganic carbon pool is assumed to be of pedogenic origin, these emissions would ultimately not alter carbon budgets. The results of this study highlight the preferential degradation of younger organic substrates in freshly thawed Yedoma, if available, and a substantial release of CO2 from inorganic sources.

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Increasing demands for small-scale radiocarbon (14C) analyses required the installation of a “SO-110 B” type ion source (HVE Europa B.V.) at our 6 MV Tandetron AMS (HVE) dedicated for the direct injection of CO2 using either the gas injection system (GIS) from Ionplus AG or a EuroVector EA 3000 elemental analyzer (EA). We tested both systems with multiple series of 14C-free and modern standards (2.5–50 µg C) combusted in quartz ampoules or EA containers and were able to quantify exogenous C introduced. In EA-GIS-AMS analysis exogenous C is mainly derived from the EA sample containers. Blank values for 50 µg C combusted in solvent-cleaned tin (Sn) vessels were 0.0127 ± 0.0012 F14C (boats) and 0.0090 ± 0.0010 F14C (capsules), while they were much higher for thermally cleaned silver (Ag) capsules. The processing of gas samples for GIS-AMS yields similar blank values corresponding to 0.30 ± 0.08 µg exogenous C with 0.93 ± 0.23 F14C consisting of 0.28 µg C modern and 0.02 µg C fossil C. The combustion of larger amounts of blank material (1 mg C) in a single quartz tube split into aliquots gives lower blanks (0.0064 ± 0.0008 F14C; 50 µg C). Thus, 14C analysis of small, gaseous samples is now possible at CologneAMS.