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Stable isotope ratios of oxygen ((18)O/(16)O) and hydrogen (D/H) in water have long been considered powerful indicators of paleoclimate. However, quantitative interpretation of isotope variations in terms of climate changes is hampered by a limited understanding of physical processes controlling the global isotope behavior. Analysis was conducted of time series of (18)O content (delta (18)O) of monthly precipitation and surface air temperature available through the International Atomic Energy Agency-World Meteorological Organization global network, "Isotopes in Precipitation." This study indicates that long-term changes of isotopic composition of precipitation over mid-and high-latitude regions during the past three decades closely followed long-term changes of surface air temperature with the average 8180-temperature coefficient around 0.6 per mil per degree Celsius.

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We present an estimate of net ecosystem exchange (NEE) of CO₂ in Europe for the years 2001 through 2007. It is derived with a data assimilation that uses a large set of atmospheric CO₂ mole fraction observations (<70 000) to guide relatively simple descriptions of terrestrial and oceanic net exchange, while fossil fuel and fire emissions are prescribed. Weekly terrestrial sources and sinks are optimized (i.e., a flux inversion) for a set of 18 large ecosystems across Europe in which prescribed climate, weather, and surface characteristics introduce finer scale gradients. We find that the terrestrial biosphere in Europe absorbed a net average of 2212165 TgC yr22121 over the period considered. This uptake is predominantly in non-EU countries, and is found in the northern coniferous (221294 TgC/yr) and mixed forests (221230 TgC yr22121) as well as the forest/field complexes of eastern Europe (221285 TgC yr22121). An optimistic uncertainty estimate derived using three biosphere models suggests the uptake to be in a range of 2212122 to 2212258 TgC yr22121, while a more conservative estimate derived from the a-posteriori covariance estimates is 2212165±437 TgC yr22121. Note however that uncertainties are hard to estimate given the nature of the system and are likely to be significantly larger than this. Interannual variability in NEE includes a reduction in uptake due to the 2003 drought followed by three years of more than average uptake. The largest anomaly of NEE occurred in 2005 concurrent with increased seasonal cycles of observed CO₂. We speculate these changes to result from the strong negative phase of the North Atlantic Oscillation in 2005 that lead to favorable summer growth conditions, and altered horizontal and vertical mixing in the atmosphere. All our results are available through http://www.carbontracker.e

As a follow-up to the meeting of experts convened at the International Atomic Energy Agency (IAEA) in February 1989, and the International 14C Workshop held in Glasgow in September 1989, the 14C Quality Assurance Program was formulated. In a joint effort of several radiocarbon teams and IAEA staff, we have prepared a set of five new intercomparison materials. These are natural materials frequently used by radiocarbon laboratories. The materials were distributed to 137 laboratories in May 1990. In February 1991, a meeting of experts was convened in Vienna to evaluate the results, to determine the radiocarbon activity of the five samples expressed in % Modern (pMC) terms and to define the 13C/12C ratio, and to make recommendations on further use of these materials. We present here the results of the exercise and the agreed consensus values for each of the five materials and discuss the different analyses that were undertaken.

The Craig-Gordon model (C-G model) [H. Craig, L.I. Gordon. Deuterium and oxygen 18 variations in the ocean and the marine atmosphere. In Stable Isotopes in Oceanographic Studies and Paleotemperatures, E. Tongiorgi (Ed.), pp. 9-130, Laboratorio di Geologia Nucleare, Pisa (1965).] has been synonymous with the isotope effects associated with the evaporation of water from surface waters, soils, and vegetations, which in turn constitutes a critical component of the global water cycle. On the occasion of the four decades of its successful applications to isotope geochemistry and hydrology, an attempt is made to: (a) examine its physical background within the framework of modern evaporation models, (b) evaluate our current knowledge of the environmental parameters of the C-G model, and (c) comment on a general strategy for the use of these parameters in field applications. Despite its simplistic representation of evaporation processes at the water-air interface, the C-G model appears to be adequate to provide the isotopic composition of the evaporation flux. This is largely due to its nature for representing isotopic compositions (a ratio of two fluxes of different isotopic water molecules) under the same environmental conditions. Among many environmental parameters that are included in the C-G model, accurate description and calculations are still problematic of the kinetic isotope effects that occur in a diffusion-dominated thin layer of air next to the water-air interface. In field applications, it is of importance to accurately evaluate several environmental parameters, particularly the relative humidity and isotopic compositions of the 'free-atmosphere', for a system under investigation over a given time-scale of interest (e.g., hourly to daily to seasonally). With a growing interest in the studies of water cycles of different spatial and temporal scales, including paleoclimate and water resource studies, the importance and utility of the C-G model is also likely to grow in the future.

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