Sub-annual measurements, eight increments per year, of cellulose in a Scots pine tree growing in central Norway are presented as a proxy for tropospheric 14CO2 at biweekly to monthly resolution. The results are validated by comparison to direct atmospheric measurements in the years 1959–1965, and a new dataset is obtained for 1953–1958. In this period, our cellulose measurements deviate from the Bomb 13 NH1 calibration curve, which is derived from single-year measurements of tree rings. This is due to seasonal cycles in tropospheric radiocarbon (14C) concentrations, caused by the first series of atmospheric nuclear weapons tests.

Speleothem organic matter can be a powerful tracer for past environmental conditions and karst processes. Carbon isotope measurements (δ13C and 14C) in particular can provide crucial information on the provenance and age of speleothem organic matter, but are challenging due to low concentrations of organic matter in stalagmites. Here, we present a method development study on extraction and isotopic characterization of speleothem organic matter using a rapid procedure with low laboratory contamination risk. An extensive blank assessment allowed us to quantify possible sources of contamination through the entire method. Although blank contamination is consistently low (1.7 ± 0.34 – 4.3 ± 0.86 μg C for the entire procedure), incomplete sample decarbonation poses a still unresolved problem of the method, but can be detected when considering both δ13C and 14C values. We test the method on five stalagmites, showing reproducible results on samples as small as 7 μg C for δ13C and 20 μg C for 14C. Furthermore, we find consistently lower non-purgeable organic carbon (NPOC) 14C values compared to the carbonate 14C over the bomb spike interval in two stalagmites from Yok Balum Cave, Belize, suggesting overprint of a pre-aged or even fossil source of carbon on the organic fraction incorporated by these stalagmites.