Reconstructing the chronology of the natural and anthropogenic uranium isotopic signals in a marine sediment core from Beppu Bay, Japan.

The long-lived U isotopes, 233U and 236U, have been used increasingly in recent years as marine circulation tracers and for identifying sources of uranium contamination in the environment. The sedimentation histories of these two U isotopes in combination with natural 238U were reconstructed for an anoxic sediment core collected from Beppu Bay, Japan, in the western North Pacific Ocean showing good time resolution (less than 2.6 y/sample). The 233U/236U atom ratio showed a prominent peak of (3.20 ± 0.30) × 10-2 around 1957 which can be attributed to the input from atmospheric nuclear weapons tests including thermonuclear tests conducting in the Equatorial Pacific. The integrated 233U/236U ratio of (1.64 ± 0.08) × 10-2 for the sediment was found to be in relatively good agreement with the representative ratio published for global fallout (∼1.4 × 10-2). A prominent increase in the authigenic ratio of 233U/238Ua,s in the leached fraction (1.39 ± 0.11 × 10-11) and the bulk digestion (1.36 ± 0.10 × 10-11) was also observed around 1957. This reflects the input supply of 233U to the seawater which is known to have a relatively constant 238U content. The authigenic 236U/238Ua,s ratio (0.18 ± 0.02 × 10-9) obtained for 1921 increased from the early 1950's to a maximum of (6.59 ± 0.60) × 10-9 around 1962. The variation in this ratio represents well the introduction history of U into the surface environment without site-specific U contamination and the time profile is also consistent with the 137Cs signature. This work thus provides a benchmark for the long-term use of the isotopic U composition as an input parameter for seawater circulation tracers and as a chronological marker for anoxic sediments and sedimentary rocks. Especially the 233U/236U ratio may serve as a key-marker for the new geological age Anthropocene.

Tracing Atlantic water transit time in the subarctic and Arctic Atlantic using 99Tc-233U-236U.

The pathway and transport time of Atlantic water passing northern Europe can be traced via anthropogenic radioisotopes released from reprocessing of spent nuclear fuels at Sellafield (SF) and La Hague (LH). These reprocessing derived radioisotopes, with extremely low natural background, are source specific and unique fingerprints for Atlantic water. This study explores a new approach using 99Tc-233U-236U tracer to estimate the transit time of Atlantic water in the coast of Greenland. We isolate the reprocessing plants (RP) signal of 236U (236URP) by incorporating 233U measurements and combine this with 99Tc which solely originates from RP, to estimate the transit time of Atlantic water circulating from Sellafield to the coast of Greenland-Iceland-Faroe Islands. Both being conservative radioisotopes, the temporal variation of 99Tc/236URP ratio in Atlantic water is only influenced by their historic discharges from RP, thus 99Tc/236URP can potentially be a robust tracer to track the transport of Atlantic water in the North Atlantic-Arctic region. Based on our observation data of 99Tc-233U-236U in seawater and the proposed 99Tc/236URP tracer approach, Atlantic water transit times were estimated to be 16-22, 25 and 25 years in the coast of Greenland, Iceland and Faroe Island, respectively. Our estimates from northeast Greenland coastal waters agree with earlier results (17-22 years). Therefore, this work provides an independent approach to estimate Atlantic water transit time with which to compare estimates from ocean modelling and other radiotracer approaches.

Correction: Novel 90Sr analysis of environmental samples by Ion-Laser InterAction Mass Spectrometry.

Correction for 'Novel 90Sr analysis of environmental samples by Ion-Laser InterAction Mass Spectrometry' by Maki Honda et al., Anal. Methods, 2022, 14, 2732-2738, https://doi.org/10.1039/D2AY00604A.

Understanding source terms of anthropogenic uranium in the Arctic Ocean - First 236U and 233U dataset in Barents Sea sediments.

This work reports the first dataset of 236U and 233U in sediment cores taken from the Barents Sea, with the aim to better understand the source terms of anthropogenic uranium in the Arctic region. Concentrations of 236U and 233U along with 137Cs, and 233U/236U atomic ratio were measured in six sediment profiles. The cumulative areal inventories of 236U and 233U obtained in this work are (3.50-12.7) × 1011 atom/m2 and (4.92-21.2) × 109 atom/m2, with averages values of (8.08 ± 2.93) × 1011 atom/m2 and (1.08 ± 0.56) × 1010 atom/m2, respectively. The total quantities of 236U and 233U deposited in the Barents Sea bottom sediments were estimated to be 507 ± 184 g and 7 ± 3 g, respectively, which are negligible compared to the total direct deposition of 236U (6000 g) and 233U (40-90 g) from global fallout in the Barents Sea. The integrated atomic ratios of 233U/236U ranging in (0.98-1.57) × 10-2 reflect the predominant global fallout signal of 236U in the Barents Sea sediments and the highest reactor-236U contribution accounts for 30 ± 14 % among the six sediment cores. The reactor-236U input in the Barents Sea sediments is most likely transported from the European reprocessing plants rather than related to any local radioactive contamination. These results provide better understanding on the source term of anthropogenic 236U in the Barents Sea, prompt the oceanic tracer application of 236U for studying the dynamics of the Atlantic-Arctic Ocean and associated climate changes. The 236U-233U benchmarked age-depth profiles seem to match reasonably well with the reported input function history of radioactive contamination in the Barents Sea, indicating the high potential of anthropogenic 236U-233U pair as a useful tool for sediment dating.

Novel 90Sr analysis of environmental samples by Ion-Laser InterAction Mass Spectrometry.

The sensitive analysis of 90Sr with accelerator mass spectrometry (AMS) was developed to advance environmental radiology. One advantage of AMS is the ability to analyze environmental samples with 90Sr/88Sr atomic ratios of 10-14 in following a simple chemical separation. Three different IAEA samples with known 90Sr concentrations (moss-soil, animal bone, Syrian soil: 1 g each) were analyzed to assess the validity of the chemical separation and the AMS measurement. The 90Sr measurements were conducted on the AMS system VERA combined with the Ion Laser InterAction Mass Spectrometry (ILIAMS) setup at the University of Vienna, which has excellent isobaric separation performance. The isobaric interference of 90Zr in the 90Sr AMS was first largely removed by chemical separation. The separation factor of Zr in two-step column chromatography with Sr resin and anion exchange resin was 106. The 90Zr remaining in the sample was effectively suppressed by ILIAMS. This procedure achieved a limit of detection <0.1 mBq in the 90Sr AMS, which is lower than typical ß-ray detection. The agreement between AMS measurements and nominal values for the 90Sr concentrations of IAEA samples indicated that the new highly-sensitive 90Sr analysis in the environmental samples with AMS is reliable.

Deciphering sources of U contamination using isotope ratio signatures in the Loire River sediments: Exploring the relevance of 233U/236U and stable Pb isotope ratios.

A broad range of contaminants has been recorded in sediments of the Loire River over the last century. Among a variety of anthropogenic activities of this nuclearized watershed, extraction of uranium and associated activities during more than 50 years as well as operation of several nuclear power plants led to industrial discharges, which could persist for decades in sedimentary archives of the Loire River. Highlighting and identifying the origin of radionuclides that transited during the last decades and were recorded in the sediments is challenging due to i) the low concentrations which are often close or below the detection limits of routine environmental surveys and ii) the mixing of different sources. The determination of the sources of anthropogenic radioactivity was performed using multi-isotopic fingerprints (236U/238U, 206Pb/207Pb and 208Pb/207Pb) and the newly developed 233U/236U tracer. For the first time 233U/236U data in a well-dated river sediment core in the French river Loire are reported here. Results highlight potential sources of contamination among which a clear signature of anthropogenic inputs related to two accidents of a former NUGG NPP that occurred in 1969 and 1980. The 233U and 236U isotopes were measured by recent high performance analytical methods due to their ultra-trace levels in the samples and show a negligible radiological impact on health and on the environment. The determination of mining activities by the use of stable Pb isotopes is still challenging probably owing to the limited dissemination of the Pb-bearing material marked by the U-ore signature downstream to the former U mines.

Deciphering anthropogenic uranium sources in the equatorial northwest Pacific margin.

This work reports the first high-resolution deposition records of anthropogenic uranium (236U and 233U) in a sediment core taken at the continental slope of the Philippine Sea off Mindanao Island in the equatorial northwest Pacific Ocean. Two notable peaks were observed in both profiles of 236U and 233U concentrations, with a narrower peak in 1951-1957 corresponding to close-in Pacific Proving Grounds (PPG) signal, and a broader peak in 1960s-1980s corresponding to the global fallout from nuclear weapons testing. 236U and 233U areal cumulative inventories in the studied sediment core are (2.79 ± 0.20) ∙ 1012 atom ∙ m-2 and (3.12 ± 0.41) ∙ 1010 atom ∙ m-2, respectively, about 20-30% of reported 233U and 236U inventories from the direct global fallout deposition. The overall 233U/236U atomic ratios obtained in this work vary within (0.3-3.5) âˆ™ 10-2, with an integrated 233U/236U atomic ratio of (1.12 ± 0.17) âˆ™ 10-2. The contribution from global fallout and close-in PPG fallout to 236U in the sediment core is estimated to be about 69% and 31%, respectively. We believe the main driving process for anthropogenic uranium deposition in the Philippine sediment is continuous scavenging of dissolved 236U from the surface seawater by sinking particles.

Anthropogenic 236U and 233U in the Baltic Sea: Distributions, source terms, and budgets.

The Baltic Sea receives substantial amounts of hazardous substances and nutrients, which accumulate for decades and persistently impair the Baltic ecosystems. With long half-lives and high solubility, anthropogenic uranium isotopes (236U and 233U) are ideal tracers to depict the ocean dynamics in the Baltic Sea and the associated impacts on the fates of contaminants. However, their applications in the Baltic Sea are hampered by the inadequate source-term information. This study reports the first three-dimensional distributions of 236U and 233U in the Baltic Sea (2018-2019) and the first long-term hindcast simulation for reprocessing-derived 236U dispersion in the North-Baltic Sea (1971-2018). Using 233U/236U fingerprints, we distinguish 236U from the nuclear weapon testing and civil nuclear industries, which have comparable contributions (142 ± 13 and 174 ± 40 g) to the 236U inventory in modern Baltic seawater. Budget calculations for 236U inputs since the 1950s indicate that, the major 236U sources in the Baltic Sea are the atmospheric fallouts (∼1.35 kg) and discharges from nuclear reprocessing plants (> 211 g), and there is a continuous sink of 236U to the anoxic sediments (589 ± 43 g). Our findings also indicate that the limited water renewal endows the Baltic Sea a strong "memory effect" retaining aged 236U signals, and the previously unknown 236U in the Baltic Sea is likely attributed to the retention of the mid-1990s' discharges from the nuclear reprocessing plants. Our preliminary results demonstrate the power of 236U-129I dual-tracer in investigating water-mass mixing and estimating water age in the Baltic Sea, and this work provides fundamental knowledge for future 236U tracer studies in the Baltic Sea.

Revisiting the Middle and Upper Palaeolithic archaeology of Gruta do Caldeirão (Tomar, Portugal).

Gruta do Caldeirão features a c. 6 m-thick archaeological stratification capped by Holocene layers ABC-D and Ea, which overlie layer Eb, a deposit of Magdalenian age that underwent significant disturbance, intrusion, and component mixing caused by funerary use of the cave during the Early Neolithic. Here, we provide an updated overview of the stratigraphy and archaeological content of the underlying Pleistocene succession, whose chronology we refine using radiocarbon and single-grain optically stimulated luminescence dating. We find a high degree of stratigraphic integrity. Dating anomalies exist in association with the succession's two major discontinuities: between layer Eb and Upper Solutrean layer Fa, and between Early Upper Palaeolithic layer K and Middle Palaeolithic layer L. Mostly, the anomalies consist of older-than-expected radiocarbon ages and can be explained by bioturbation and palimpsest-forming sedimentation hiatuses. Combined with palaeoenvironmental inferences derived from magnetic susceptibility analyses, the dating shows that sedimentation rates varied in tandem with the oscillations in global climate revealed by the Greenland oxygen isotope record. A steep increase in sedimentation rate is observed through the Last Glacial Maximum, resulting in a c. 1.5 m-thick accumulation containing conspicuous remains of occupation by people of the Solutrean technocomplex, whose traditional subdivision is corroborated: the index fossils appear in the expected stratigraphic order; the diagnostics of the Protosolutrean and the Lower Solutrean predate 24,000 years ago; and the constraints on the Upper Solutrean place it after Greenland Interstadial 2.2. (23,220-23,340 years ago). Human usage of the site during the Early Upper and the Middle Palaeolithic is episodic and low-intensity: stone tools are few, and the faunal remains relate to carnivore activity. The Middle Palaeolithic is found to persist beyond 39,000 years ago, at least three millennia longer than in the Franco-Cantabrian region. This conclusion is upheld by Bayesian modelling and stands even if the radiocarbon ages for the Middle Palaeolithic levels are removed from consideration (on account of observed inversions and the method's potential for underestimation when used close to its limit of applicability). A number of localities in Spain and Portugal reveal a similar persistence pattern. The key evidence comes from high-resolution fluviatile contexts spared by the site formation issues that our study of Caldeirão brings to light-palimpsest formation, post-depositional disturbance, and erosion. These processes. are ubiquitous in the cave and rock-shelter sites of Iberia, reflecting the impact on karst archives of the variation in climate and environments that occurred through the Upper Pleistocene, and especially at two key points in time: between 37,000 and 42,000 years ago, and after the Last Glacial Maximum. Such empirical difficulties go a long way towards explaining the controversies surrounding the associated cultural transitions: from the Middle to the Upper Palaeolithic, and from the Solutrean to the Magdalenian. Alongside potential dating error caused by incomplete decontamination, proper consideration of sample association issues is required if we are ever to fully understand what happened with the human settlement of Iberia during these critical intervals, and especially so with regards to the fate of Iberia's last Neandertal populations.

70-Year Anthropogenic Uranium Imprints of Nuclear Activities in Baltic Sea Sediments.

A strongly stratified water structure and a densely populated catchment make the Baltic Sea one of the most polluted seas. Understanding its circulation pattern and time scale is essential to predict the dynamics of hypoxia, eutrophication, and pollutants. Anthropogenic 236U and 233U have been demonstrated as excellent transient tracers in oceanic studies, but unclear input history and inadequate long-term monitoring records limit their application in the Baltic Sea. From two dated Baltic sediment cores, we obtained high-resolution records of anthropogenic uranium imprints originating from three major human nuclear activities throughout the Atomic Era. Using the novel 233U/236U signature, we distinguished and quantified 236U inputs from global fallout (45.4-52.1%), Chernobyl accident (0.3-1.8%), and discharges from civil nuclear industries (46.1-54.3%) to the Baltic Sea. We estimated the total release of 233U (7-15 kg) from the atmospheric nuclear weapon testing and pinpointed the 233U peak signal in the mid-to-late 1950s as a potential time marker for the onset of the Anthropocene Epoch. This work also provides fundamental 236U data on Chernobyl accident and early discharges from civil nuclear facilities, prompting worldwide 233U-236U tracer studies. We anticipate our data to be used in a broader application in model-observation interdisciplinary research on water circulation and pollutant dynamics in the Baltic Sea.

An unknown source of reactor radionuclides in the Baltic Sea revealed by multi-isotope fingerprints.

We present an application of multi-isotopic fingerprints (i.e., 236U/238U, 233U/236U, 236U/129I and 129I/127I) for the discovery of previously unrecognized sources of anthropogenic radioactivity. Our data indicate a source of reactor 236U in the Baltic Sea in addition to inputs from the two European reprocessing plants and global fallout. This additional reactor 236U may come from unreported discharges from Swedish nuclear research facilities as supported by high 236U levels in sediment nearby Studsvik, or from accidental leakages of spent nuclear fuel disposed on the Baltic seafloor, either reported or unreported. Such leakages would indicate problems with the radiological safety of seafloor disposal, and may be accompanied by releases of other radionuclides. The results demonstrate the high sensitivity of multi-isotopic tracer systems, especially the 233U/236U signature, to distinguish environmental emissions of unrevealed radioactive releases for nuclear safeguards, emergency preparedness and environmental tracer studies.

On the Quality Control for the Determination of Ultratrace-Level 236U and 233U in Environmental Samples by Accelerator Mass Spectrometry.

Our recent attempt to determine ultratrace-level 236U and 233U in small-volume seawater samples was challenged by high and unstable procedure blanks in our environmental radioactivity laboratory, which used to be a spent fuel research facility. Through intercomparison experiments with different laboratories and background checks on the chemical reagents and laboratory dust, the resuspended U-bearing dust was identified as the dominating source of the 236U and 233U contamination. With the implementation of background control (especially dust control) measures, the procedure blanks and detection limits of 236U and 233U for the radiochemical separation procedure have been significantly improved by three orders of magnitudes. With well-controlled blanks, the analytical precision for 236U and 233U predominantly relies on the AMS counting statistics. Background check and dust control are strongly recommended before the analyses of environmental-level long-lived radionuclides (such as 236U and 233U) that are conducted in the former or active nuclear facilities, even if clearance of radioactivity relevant for radioprotection was achieved.

First dataset of 236U and 233U around the Greenland coast: A 5-year snapshot (2012-2016).

We report the first combined dataset of 236U and 233U in the Greenland marine environment during the period of 2012-2016. Results are discussed in terms of time evolution and spatial distribution of 236U concentration, and atomic ratios of 236U/238U and 233U/236U. 236U concentrations along the Greenland coast are distributed within a relatively narrow range of (0.7-12.9) × 107 atom/L, corresponding to 236U/238U atomic ratios of (1.1-15.5) × 10-9. The 233U/236U atomic ratios obtained vary from 0.12 × 10-2 to 1.16 × 10-2, with the majority distributed in the range of (0.2-0.7) × 10-2. We applied 233U/236U and 236U/238U atomic ratios in a binary mixing model to identify possible 236U source terms. The results indicate that anthropogenic 236U and 233U in Greenland surface seawater originated from the direct global fallout (DGF) and the Sellafield and La Hague reprocessing plants (RP) is diluted by a third endmember, mostly likely natural ocean water (NOW), containing marginal 236U and 233U. A preliminary estimation of the source terms of 236U using 233U/236U atomic ratios indicate that, for both eastern and western Greenland seawater, contributions from global fallout (GF) constitute about 30% of 236U. The dominating source for 236U, i.e. 70 %, is associated to reactor 236U including discharges from RP and local reactor input in the Arctic Ocean.

Pushing Limits of ICP-MS/MS for the Determination of Ultralow 236U/238U Isotope Ratios.

Determination of uranium isotope ratios is of great expedience for assessing its origin in environmental samples. In particular, the 236U/238U isotope ratio provides a powerful tool to discriminate between the different sources of uranium (uranium ore, geochemical background, and uranium from anthropogenic activities). However, in the environment, this ratio is typically below 10-8. This low abundance of 236U and the presence in large excess of major isotopes (mainly 238U and 235U) complicates the accurate detection of 236U signal by mass spectrometry and thus highly sensitive analytical instruments providing high abundance sensitivity are required. This work pushes the limits of triple quadrupole-based ICP-MS technology for accurate detection of 236U/238U isotope ratios down to 10-10, which is so far mainly achievable by AMS. Coupled with an efficient desolvating module, N2O was used as the reaction gas in the collision reaction cell of the ICP-MS/MS. This configuration allows a significant decrease of the uranium polyatomic interferences (235UH+ ions) and an accurate determination of low 236U/238U isotope ratios. This new methodology was successfully validated through measurements of certified reference material from 10-7 to 10-9 and then through comparisons with AMS measurement results for ratios down to 10-10. This is the first time that 236U/238U isotope ratios as low as 10-10 were determined by ICP-MS/MS. The possibility of measuring low 236U/238U isotope ratios can offer a large variety of geochemical applications in particular for the determination of uranium sources in the environment.

Radiocarbon analysis of carbonaceous aerosols in Bratislava, Slovakia.

Aerosols dispersed in the atmosphere represent important factors influencing not only the environment, but also human health. Carbonaceous aerosols are one of the main components of total atmospheric aerosols, and their sources are of great interest. Radiocarbon analysis provides an excellent way to determine the fraction of fossil and non-fossil aerosols in the atmosphere. Over the period of one year (June 2017-June 2018), we sampled atmospheric aerosols with size greater than 0.3 µm in Bratislava, Slovakia and used the exposed quartz filters for radiocarbon analysis of the elemental carbon (EC) aerosol fraction. The results show that on average the fossil fuel combustion is the dominant source of EC aerosol particles in Bratislava. In summer months, they represent more than half (65-80%) of the total EC aerosols. The relative amount of EC particles derived from biomass burning was 20-35% in summer, which increased to 40-55% in winter months. The dominance of fossil fraction is caused by high degree of industrialization and urbanization of the city. The increase of biomass fraction in winter is probably caused by domestic wood burning in areas surrounding the Bratislava city.

Radionuclides in surface waters around the damaged Fukushima Daiichi NPP one month after the accident: Evidence of significant tritium release into the environment.

Following the Fukushima nuclear accident (2011), radionuclides mostly of volatile elements (e.g., 131I, 134,137Cs, 132Te) have been investigated frequently for their presence in the atmosphere, pedosphere, biosphere, and the Pacific Ocean. Smaller releases of radionuclides with intermediate volatility, (e.g., 90Sr), have been reported for soil. However, few reports have been published which targeted the contamination of surface (fresh) waters in Japan soon after the accident. In the present study, 10 surface water samples (collected on April 10, 2011) have been screened for their radionuclide content (3H, 90Sr, 129I, 134Cs, and 137Cs), revealing partly unusually high contamination levels. Especially high tritium levels (184 ±â€¯2 Bq·L-1; the highest levels ever reported in scientific literature after Fukushima) were found in a puddle water sample from close to the Fukushima Daiichi nuclear power plant. The ratios between paddy/puddle water from one location only a few meters apart vary around 1% for 134Cs, 12% for 129I (131I), and around 40% for both 3H and 90Sr. This illustrates the adsorption of radiocesium on natural minerals and radioiodine on organic substances (in the rice paddy), whereas the concentration differences of 3H and 90Sr between the two waters are mainly dilution driven.

Radiocarbon re-dating of contact-era Iroquoian history in northeastern North America.

A time frame for late Iroquoian prehistory is firmly established on the basis of the presence/absence of European trade goods and other archeological indicators. However, independent dating evidence is lacking. We use 86 radiocarbon measurements to test and (re)define existing chronological understanding. Warminster, often associated with Cahiagué visited by S. de Champlain in 1615-1616 CE, yields a compatible radiocarbon-based age. However, a well-known late prehistoric site sequence in southern Ontario, Draper-Spang-Mantle, usually dated ~1450-1550, yields much later radiocarbon-based dates of ~1530-1615. The revised time frame dramatically rewrites 16th-century contact-era history in this region. Key processes of violent conflict, community coalescence, and the introduction of European goods all happened much later and more rapidly than previously assumed. Our results suggest the need to reconsider current understandings of contact-era dynamics across northeastern North America.

Limits on Supernova-Associated

We searched for the presence of ^{26}Al in deep-sea sediments as a signature of supernova influx. Our data show an exponential dependence of ^{26}Al with the sample age that is fully compatible with radioactive decay of terrigenic ^{26}Al. The same set of samples demonstrated a clear supernova ^{60}Fe signal between 1.7 and 3.2 Myr ago. Combining our ^{26}Al data with the recently reported ^{60}Fe data results in a lower limit of 0.18_{-0.08}^{+0.15} for the local interstellar ^{60}Fe/^{26}Al isotope ratio. It compares to most of the ratios deduced from nucleosynthesis models and is within the range of the observed average galactic ^{60}Fe/^{26}Al flux ratio of (0.15±0.05).

The increase of soil organic carbon as proposed by the "4/1000 initiative" is strongly limited by the status of soil development - A case study along a substrate age gradient in Central Europe.

During COP 21 in Paris 2015, several states and organizations agreed on the "4/1000" initiative for food security and climate. This initiative aims to increase world's soil organic carbon (SOC) stocks by 4‰ annually. The influence of soil development status on SOC dynamics is very important but usually not considered in studies. We analyse SOC accumulation under forest, grassland and cropping systems along a soil age gradient (10-17,000years) to show the influence of soil development status on SOC increase. SOC stocks (0-40cm) and accumulation rates along a chronosequence in alluvial soils of the Danube River in the Marchfeld (eastern Austria) were analysed. The analysed Fluvisols and Chernozems have been used as forest, grassland and cropland for decades or hundreds of years. The results showed that there is a fast build-up of OC stocks (0-40cm) in young soils with accumulation of ~1.3tha-1a-1 OC in the first 100years and ~0.5tha-1a-1 OC between 100 and 350years almost independent of land use. Chernozems with a sediment deposition age older than 5.000years have an accumulation rate<0.01tOCha-1a-1 (0-40cm). Radiocarbon dating showed that the topsoil (0-10cm) consists mainly of ">modern" and "modern" carbon indicating a fast carbon cycling. Carbon in subsoil is less exposed to decomposition and OC can be stored at long-time scales in the subsoil (14C age of 3670±35 BP). In view of the '4/1000' initiative, soils with constant carbon input (forest & grassland) fulfil the intended 4‰ growth rate of SOC stocks only in the first 60years of soil development. We proclaim that under the present climate in Central Europe, the increase of SOC stocks in soil is strongly affected by the state of soil development.