Phenomena related to the natural carbon cycle as the 14C distribution between atmosphere and ocean and the atmospheric response to the input of fossil fuel CO2 and of 14C produced in nuclear weapon tests have been quantitatively discussed by other authors using box models. However the exchange coefficients derived from the natural 14C distribution do not agree with those valid to describe the short‐term phenomena. A model consisting of a well mixed atmospheric box coupled to a long‐term biosphere, of an ocean surface box and a diffusive deep ocean is discussed. The dynamic parameters were derived from the preindustrial 14C distribution in atmosphere and ocean. A consistent description of phenomena with completely different characteristic times is possible, because in the box diffusion model the flux from mixed layer to deep sea increases for decreasing time constants of the perturbations. This is in contrary to box models where it is essentially independent of the time constants if they are smaller than a few hundred years. Due to this fact our model is valid for predictions of the atmospheric CO2 response to the various possible future CO2 input time functions.

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Abstract. Sublimation dominates the ablation process on cold, high-altitude glaciers in the tropical Andes. Transport of water vapor through the firn and exchange with ambient moisture alter the stable isotope composition of the surface layers. A sublimation experiment carried out during an ice core drilling campaign on Cerro Tapado (5536 m above sea level, 30ø08'S, 69ø55'W) revealed a strong enrichment in the 2H and •80 content in the surface layer. Concerning the deuterium excess, a decrease occurred at daytime, while during the night, the values remained comparatively constant. At daytime the sublimation is enhanced due to the higher moisture deficit of the ambient air accompanied by relatively high firn surface temperatures. Low surface temperatures at night cause condensation of water vapor in the firn pores near the surface and thus inhibit penetration of the isotopically enriched surface front into deeper firn layers. Measuring an isotope profile obtained through detailed sampling between the surface and 38 cm depth proved this mechanism. The observed modification of the isotopic composition at the surface was quantitatively described by a model, which also reproduced the mass loss measured with sublimation pans and calculated from relevant meteorological data. The results of this study suggest that the influence of sublimation on the preserved isotope record of ice cores under comparable environmental conditions is rather limited. In any case, simultaneous measurements of 82H and 8•80 help to identify layers in an ice core which might be effected by sublimation. However, since the mass loss due to sublimation was of the order of 2-4 mm per day during the experiment, important palaeoinformation from an isotope record could be eliminated during extended dry periods.

Ice cores drilled from glaciers around the world generally contain horizons with elevated levels of beta radioactivity including 36Cl and 3H associated with atmospheric thermonuclear bomb testing in the 1950s and 1960s. Ice cores collected in 2006 from Naimona'nyi Glacier in the Himalaya (Tibet) lack these distinctive marker horizons suggesting no net accumulation of mass (ice) since at least 1950. Naimona'nyi is the highest glacier (6050 masl) documented to be losing mass annually suggesting the possibility of similar mass loss on other high‐elevation glaciers in low and mid‐latitudes under a warmer Earth scenario. If climatic conditions dominating the mass balance of Naimona'nyi extend to other glaciers in the region, the implications for water resources could be serious as these glaciers feed the headwaters of the Indus, Ganges, and Brahmaputra Rivers that sustain one of the world's most populous regions.

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[1] Isotope records from Andean ice cores provide detailed and high-resolution climate information on various time scales. However, the relationship between these valuable isotope records and local or regional climate remains poorly understood. Here we present results from two new drillings in Bolivia, from the Illimani and the Sajama ice caps. All four high altitude isotope signals in the Andes now available (Huascarán, Quelccaya, Illimani and Sajama) show near identical decadal variability in the 20th century.Comparison with general circulation model results and meteorological data suggest that the Andean high altitude records are primarily controlled by precipitation variability over the Amazon basin.

Cr, Cu, Zn, Co, Ni, Mo, Rh, Pd, Ag, Cd, Sb, Pt, Au, and U have been determined in clean room conditions by inductively coupled plasma sector field mass spectrometry and other analytical techniques, in various sections of two dated snow/ice cores from the high-altitude (4450 m asl) glacier saddle Colle Gnifetti, Monte Rosa massif, located in the Swiss-Italian Alps. These cores cover a 350-year time period, from 1650 to 1994. The results show highly enhanced concentrations for most metals in snow/ice dated from the second half of the 20th century, compared with concentrations in ancient ice dated from the 17th and 18th centuries. The highest increase factors from the pre-1700 period to the post-1970 period are observed for Cd (36), Zn (19), Bi (15), Cu (11), and Ni (9), confirming the importance of atmospheric pollution by heavy metals in Europe. Metal concentrations observed in Colle Gnifetti snow around 1980 appear to be quantitatively related to metal emissions from Italy, Switzerland, Germany, France, Belgium, and Austria at that time, making it possible to reconstruct past changes in metal emission in these countries during the last centuries.

Lead concentrations and lead isotope ratios were analyzed in two firn/ice cores covering the period from 1650 to 1994, which were obtained from the 4450 m high glacier saddle Colle Gnifetti located in the Monte Rosa massif at the Swiss−Italian border. This study presents the first glaciochemical time series with annual resolution, spanning several centuries of lead concentrations and lead isotopic compositions in precipitation in Europe. Lead concentrations in firn dated from the 1970s are ∼25 times higher than in ice dated from the 17th century, confirming the massive rise in lead pollution in Europe during the last few centuries. A decline of the lead concentration is then observed during the last two decades, i.e., from 1975 to 1994. The lead isotope ratio 206Pb/207Pb decreased from about 1.18 in the 17th and 18th centuries to about 1.12 in the 1970s. These variations are in good agreement with available information on variations in anthropogenic lead emissions from West European countries, especially from the use of lead additives in gasoline.