Abstract. The aim of this paper is to provide the community with a comprehensive overview of the studies of glaciers in the tropical Andes conducted in recent decades leading to the current status of the glaciers in the context of climate change. In terms of changes in surface area and length, we show that the glacier retreat in the tropical Andes over the last three decades is unprecedented since the maximum extension of the Little Ice Age (LIA, mid-17th-early 18th century). In terms of changes in mass balance, although there have been some sporadic gains on several glaciers, we show that the trend has been quite negative over the past 50 yr, with a mean mass balance deficit for glaciers in the tropical Andes that is slightly more negative than the one computed on a global scale. A break point in the trend appeared in the late 1970s with mean annual mass balance per year decreasing from −0.2 m w.e. in the period 1964-1975 to −0.76 m w.e. in the period 1976-2010. In addition, even if glaciers are currently retreating everywhere in the tropical Andes, it should be noted that this is much more pronounced on small glaciers at low altitudes that do not have a permanent accumulation zone, and which could disappear in the coming years/decades. Monthly mass balance measurements performed in Bolivia, Ecuador and Colombia show that variability of the surface temperature of the Pacific Ocean is the main factor governing variability of the mass balance at the decadal timescale. Precipitation did not display a significant trend in the tropical Andes in the 20th century, and consequently cannot explain the glacier recession.Published by Copernicus Publications on behalf of the European Geosciences Union. A. Rabatel et al.: Current state of glaciers in the tropical AndesOn the other hand, temperature increased at a significant rate of 0.10 • C decade −1 in the last 70 yr. The higher frequency of El Niño events and changes in its spatial and temporal occurrence since the late 1970s together with a warming troposphere over the tropical Andes may thus explain much of the recent dramatic shrinkage of glaciers in this part of the world.

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.

Abstract. Accurate measurement of black carbon (BC) mass concentrations in snow and ice is crucial for the assessment of climatic impacts. However, it is difficult to compare methods used to assess BC levels in the literature as they are not the same. The single particle soot photometer (SP2) method appears to be one of the most suitable to measure low concentrations of BC in snow and ice. In this paper, we evaluated a method for the quantification of refractory BC (rBC) in snow and ice samples coupling the SP2 with the APEX-Q nebulizer. The paper reviews all the steps of rBC determination, including SP2 calibration, correction for rBC particle aerosolization efficiency (75 ± 7% using the APEX-Q nebulizer), and treatment of the samples. In addition, we compare the SP2 method and the thermal–optical method – Sunset organic carbon (OC) / elemental carbon (EC) aerosol analyzer with EUSAAR2 protocol – using snow and firn samples with different characteristics from the Greenland Summit, the French Alps, the Caucasus, and the Himalayas. Careful investigation was undertaken of analytical artifacts that potentially affect both methods. The SP2-based rBC quantification may be underestimated when the SP2 detection range does not cover correctly the existing size distribution of the sample. Thermal–optical EC measurements can be underestimated by low filtration efficiency of quartz fiber filter before analysis or dust properties (concentration and type), and overestimated by pyrolyzed OC artifacts during EC analysis. These results underline the need for careful assessment of the analytical technique and procedure for correct data interpretation.

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Abstract. This paper presents the light-scattering properties of atmospheric aerosol particles measured over the past decade at 28 ACTRIS observatories, which are located mainly in Europe. The data include particle light scattering (σsp) and hemispheric backscattering (σbsp) coefficients, scattering Ångström exponent (SAE), backscatter fraction (BF) and asymmetry parameter (g). An increasing gradient of σsp is observed when moving from remote environments (arctic/mountain) to regional and to urban environments. At a regional level in Europe, σsp also increases when moving from Nordic and Baltic countries and from western Europe to central/eastern Europe, whereas no clear spatial gradient is observed for other station environments. The SAE does not show a clear gradient as a function of the placement of the station. However, a west-to-east-increasing gradient is observed for both regional and mountain placements, suggesting a lower fraction of fine-mode particle in western/south-western Europe compared to central and eastern Europe, where the fine-mode particles dominate the scattering. The g does not show any clear gradient by station placement or geographical location reflecting the complex relationship of this parameter with the physical properties of the aerosol particles. Both the station placement and the geographical location are important factors affecting the intra-annual variability. At mountain sites, higher σsp and SAE values are measured in the summer due to the enhanced boundary layer influence and/or new particle-formation episodes. Conversely, the lower horizontal and vertical dispersion during winter leads to higher σsp values at all low-altitude sites in central and eastern Europe compared to summer. These sites also show SAE maxima in the summer (with corresponding g minima). At all sites, both SAE and g show a strong variation with aerosol particle loading. The lowest values of g are always observed together with low σsp values, indicating a larger contribution from particles in the smaller accumulation mode. During periods of high σsp values, the variation of g is less pronounced, whereas the SAE increases or decreases, suggesting changes mostly in the coarse aerosol particle mode rather than in the fine mode. Statistically significant decreasing trends of σsp are observed at 5 out of the 13 stations included in the trend analyses. The total reductions of σsp are consistent with those reported for PM2.5 and PM10 mass concentrations over similar periods across Europe.

Abstract. We applied a climate-chemistry global model to evaluate the impact of black carbon (BC) deposition on the Himalayan snow cover from 1998 to 2008. Using a stretched grid with a resolution of 50 km over this complex topography, the model reproduces reasonably well the remotely sensed observations of the snow cover duration. Similar to observations, modelled atmospheric BC concentrations in the central Himalayas reach a minimum during the monsoon and a maximum during the post-and pre-monsoon periods. Comparing the simulated BC concentrations in the snow with observations is more challenging because of their high spatial variability and complex vertical distribution. We simulated spring BC concentrations in surface snow varying from tens to hundreds of µg kg −1 , higher by one to two orders of magnitude than those observed in ice cores extracted from central Himalayan glaciers at high elevations (> 6000 m a.s.l.), but typical for seasonal snow cover sampled in middle elevation regions (< 6000 m a.s.l.). In these areas, we estimate that both wet and dry BC depositions affect the Himalayan snow cover reducing its annual duration by 1 to 8 days. In our simulations, the effect of anthropogenic BC deposition on snow is quite low over the Tibetan Plateau because this area is only sparsely snow covered. However, the impact becomes larger along the entire Hindu-Kush, Karakorum and Himalayan mountain ranges. In these regions, BC in snow induces an increase of the net short-wave radiation at the surface with an annual mean of 1 to 3 W m −2 leading to a localised warming between 0.05 and 0.3 • C.

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Abstract.A shallow ice core was extracted at the summit of Mera Peak at 6376 m a.s.l. in the southern flank of the Nepalese Himalaya range. From this core, we reconstructed the seasonal deposition fluxes of dust and refractory black carbon (rBC) since 1999. This archive presents well preserved seasonal cycles based on a monsoonal precipitation pattern. According to the seasonal precipitation regime in which 80 % of annual precipitation falls between June and September, we estimated changes in the concentrations of these aerosols in surface snow. The analyses revealed that mass fluxes are a few orders of magnitude higher for dust (10.4 ± 2.8 g m −2 yr −1 ) than for rBC (7.9 ± 2.8 mg m −2 yr −1 ). The relative lack of seasonality in the dust record may reflect a high background level of dust inputs, whether from local or regional sources. Over the 10-year record, no deposition flux trends were detected for any of the species of interest. The data were then used to simulate changes in the surface snow albedo over time and the potential melting caused by these impurities. Mean potential melting caused by dust and rBC combined was 713 kg m −2 yr −1 , and for rBC alone, 342 kg m −2 yr −1 for rBC under certain assumptions. Compared to the melting rate measured using the mass and energy balance at 5360 m a.s.l. on Mera Glacier between November 2009 and October 2010, i.e. 3000 kg m −2 yr −1 and 3690 kg m −2 yr −1 respectively, the impact of rBC represents less than 16 % of annual potential melting while the contribution of dust and rBC combined to surface melting represents a maximum of 26 %. Over the 10-year period, rBC variability in the ice core signal primarily reflected variability of the monsoon signal rather than variations in the intensity of emissions.