Over the course of one year (2021), we monitored the carbon isotope composition of atmospheric CO2 at three locations in Croatia: the Adriatic port city of Rijeka (Cfa climate) and at two rural sites: Gornje Jelenje (Cfb climate) in the vicinity of a main road and clean-air site Parg (Dfb climate). Carbon isotope composition at all sites shows seasonal variation, ranging from –41.3 to 25.2‰ for Δ14C and from –13.1 to –11.3‰ for δ13C. Rijeka systematically has the lowest and Parg the highest Δ14C, and δ13C at the sites are not statistically different one from another. The Δ14C of leaves of deciduous trees reflect the trend of atmospheric Δ14C. Based on the assumption that the investigated area is under the influence of two main sources of CO2: fossil and natural (sea exchange, biosphere, and undisturbed – clean air atmospheric component) the approximate share of fossil CO2 in total atmospheric CO2 has been estimated for Rijeka (2.1 ± 1.3%) and Gornje Jelenje (1.0 ± 0.9%). Comparison of our results with the data from European CO2 sampling stations indicates strong influence of CO2 from sea and biosphere. Backward trajectories indicate a possibility of Δ14CCO2 contribution from distant EU nuclear power plants, but movement of air masses should be considered in more detail to confirm this.

Reliable radiocarbon (14C) ages of foraminifera are a prerequisite to generate robust high-resolution age-depth models or to obtain precise understanding of past carbon cycle dynamics. With the advance of small-scale 14C measurements, instrumental precision and levels of contamination (extraneous carbon introduced during sample pretreatment or analysis) became increasingly important to consider. To reduce the effect of carbon contamination, an attempt can be made to remove it by leaching the surface with weak acids. Alternatively, mathematical corrections (e.g., subtraction) based on processing blanks can be applied. We report on 14C analyses of monospecific foraminifera samples compared between different blank corrections (correction against 14C-free CO2, IAEA-C1 and foraminifera) and sample treatments (i) to examine whether chemical pretreatment and mathematical blank subtraction are comparable, and (ii) to determine limitations hindering reliable 14C dating with ever smaller sample sizes. The data show that chemical pretreatment of foraminifera corrected against IAEA-C1 does remove surface contamination and that the same effect can be achieved for untreated samples that were mathematically corrected for blank values determined from sample size-matched 14C-free foraminifera. Leaching only has a beneficial effect on 14C data for older samples, where the isotopic difference between untreated and chemically pretreated samples exceeds the analytical precision.

Radiocarbon (14C) generated by the thermonuclear tests in the late 1950s to early 1960s has been used as a tracer to study atmospheric and oceanic circulations, carbon exchange between different reservoirs, and fossil fuel emissions. Here we report the first measurements of 14C in atmospheric CO2 of maritime air collected over the South China Sea (SCS) during July 2014. We also present 14C of the dissolved inorganic carbon (DIC) in the sea surface water in the same region. Most of the Δ14C values of the atmospheric CO2 vary in the range of 15.6±1.6‰– 22.0±1.6‰, indicating that the central SCS maritime air is well-mixed and consistent with the clean background air in the Northern Hemisphere. The 14C values of the DIC (DI14C) in the surface seawater vary between 28.3±2.5‰ and 40.6±2.7‰, mainly due to the lateral mixing between the SCS and western Pacific. The average surface seawater DI14C is 15.4 ± 5.1‰ higher than that of the maritime air 14CO2. The reversal of the sea–air Δ14C gradient occurred at ∼2000, marking the start of the upper ocean transferring bomb 14C back to the atmosphere in the SCS.