The main symptom observed in patients with HF is exercise intolerance, consequent not only to dyspnoea but also to severe skeletal muscle weakness (both in the limb and respiratory systems), with the latter being a robust predictor of quality of life and prognosis.3 Interestingly, initial evidence from independent studies indicates that some but not all skeletal

A more developed and modern technology replaced the old radiocarbon measuring methods in Hungary, based on isotope separation by accelerator mass spectrometry (AMS) and not on activity measurements. In summer 2011, the EnvironMICADAS was successfully installed in the Laboratory of HEKAL, Debrecen, Hungary. In this project, a multipurpose gas-handling system was developed for the gas ion source of EnvironMICADAS at ETH Zürich, designed for the measurement of small environmental origin samples (<50 μg carbon) with moderate precision requirements. The ultimate aim is an automated device for high sample throughput. Since its final installation and first year of operation, over 2000 graphite targets were analyzed. Long-term stability of the instrument is confirmed through measurements of the Ox-II standard and processed blank targets during the first half of 2012.

The radiocarbon (14C) calibration curve so far contains annually resolved data only for a short period of time. With accelerator mass spectrometry (AMS) matching the precision of decay counting, it is now possible to efficiently produce large datasets of annual resolution for calibration purposes using small amounts of wood. The radiocarbon intercomparison on single-year tree-ring samples presented here is the first to investigate specifically possible offsets between AMS laboratories at high precision. The results show that AMS laboratories are capable of measuring samples of Holocene age with an accuracy and precision that is comparable or even goes beyond what is possible with decay counting, even though they require a thousand times less wood. It also shows that not all AMS laboratories always produce results that are consistent with their stated uncertainties. The long-term benefits of studies of this kind are more accurate radiocarbon measurements with, in the future, better quantified uncertainties.

Atmospheric CO2 samples have been collected by the Trondheim Radiocarbon Laboratory since the 1960s. The remaining material from the measurements has been precipitated as CaCO3 and stored in glass containers. We investigated some of the stored samples to assess whether the material could still be used for remeasurements of atmospheric radiocarbon (14C) content, or if it has been contaminated during the years of storage. We attempted different methods to clean the carbonate and release the CO2 for new measurements. The results indicate that the older samples before 1970 show a significant change in 14C content compared to the original measurements, and that our cleaning methods have only little effect. Later samples from the 1970s, which were archived in glass containers with a different lid, show a lower contamination that, however, still leads to an added uncertainty of several pMC and makes these samples unreliable.

The Trondheim radiocarbon (14C) laboratory has evolved from a traditional radiocarbon decay counting laboratory to an accelerator mass spectrometry (AMS) facility primarily measuring 14C. This evolution required adjustments in sample preparation and data handling to match the capacity of the AMS system and reduction in sample sizes to about 1 mgC. We summarize here the steps involved in dating a sample at the National Laboratory for Age Determination in Trondheim, Norway. These include the structure of our sample database for information handling, sample cleaning procedures for different sample types, our reduction systems, both an automated EA-based system for regular use and a manual system for more challenging samples, and data evaluation. We will also briefly summarize the capabilities of our isotope-ratio mass spectrometer.

No abstract

No abstract

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.