Search

We present results from a systematic study of vertical profiles of aerosol number size distribution and black carbon (BC) concentrations conducted in the Arctic, over Ny-Ålesund (Svalbard). The campaign lasted 2 years (2011-2012) and resulted in 200 vertical profiles measured by means of a tethered balloon (up to 1200 m a.g.l.) during the spring and summer seasons. In addition, chemical analysis of filter samples, aerosol size distribution and a full set of meteorological parameters were determined at ground. The collected experimental data allowed a classification of the vertical profiles into different typologies, which allowed us to describe the seasonal phenomenology of vertical aerosol properties in the Arctic. During spring, four main types of profiles were found and their behavior was related to the main aerosol and atmospheric dynamics occurring at the measuring site. Background conditions generated homogenous profiles. Transport events caused an increase of aerosol concentration with altitude. High Arctic haze pollution trapped below thermal inversions promoted a decrease of aerosol concentration with altitude. Finally, ground-based plumes of locally formed secondary aerosol determined profiles with decreasing aerosol concentration located at different altitude as a function of size. During the summer season, the impact from shipping caused aerosol and BC pollution plumes to be constrained close to the ground, indicating that increasing shipping emissions in the Arctic could bring anthropogenic aerosol and BC in the Arctic summer, affecting the climate.

Size-segregated particle samples were collected in the Arctic (Ny-Ålesund, Svalbard) in April 2011 both at ground level and in the free atmosphere exploiting a tethered balloon equipped also with an optical particle counter (OPC) and meteorological sensors. Individual particle properties were investigated by scanning electron microscopy coupled with energy dispersive microanalysis (SEM-EDS). Results of the SEM-EDS were integrated with particle size and optical measurements of the aerosols properties at ground level and along the vertical profiles. Detailed analysis of two case studies reveals significant differences in composition despite the similar structure (layering) and the comparable texture (grain size distribution) of particles in the air column. Differences in the mineral chemistry of samples point at both local (plutonic/metamorphic complexes in Svalbard) and remote (basic/ultrabasic magmatic complexes in Greenland and/or Iceland) geological source regions for dust. Differences in the particle size and shape are put into relationship with the mechanism of particle formation, that is, primary (well sorted, small) or secondary (idiomorphic, fine to coarse grained) origin for chloride and sulfate crystals and transport/settling for soil (silicate, carbonate and metal oxide) particles. The influence of size, shape, and mixing state of particles on ice nucleation and radiative properties is also discussed.

Size-segregated particle samples were collected in the Arctic (Ny-Ålesund, Svalbard) in April 2011 both at ground level and in the free atmosphere exploiting a tethered balloon equipped also with an optical particle counter (OPC) and meteorological sensors. Individual particle properties were investigated by scanning electron microscopy coupled with energy dispersive microanalysis (SEM-EDS). Results of the SEM-EDS were integrated with particle size and optical measurements of the aerosols properties at ground level and along the vertical profiles. Detailed analysis of two case studies reveals significant differences in composition despite the similar structure (layering) and the comparable texture (grain size distribution) of particles in the air column. Differences in the mineral chemistry of samples point at both local (plutonic/metamorphic complexes in Svalbard) and remote (basic/ultrabasic magmatic complexes in Greenland and/or Iceland) geological source regions for dust. Differences in the particle size and shape are put into relationship with the mechanism of particle formation, that is, primary (well sorted, small) or secondary (idiomorphic, fine to coarse grained) origin for chloride and sulfate crystals and transport/settling for soil (silicate, carbonate and metal oxide) particles. The influence of size, shape, and mixing state of particles on ice nucleation and radiative properties is also discussed.

Moderate-Resolution Imaging spectroradiometer (MODIS) land surface temperatures in Antarctica were processed in order to produce a gridded data set at 25 km resolution, spanning the period 2000-2011 at an hourly time step. The Aqua and Terra orbits and MODIS swath width, combined with frequent clear-sky conditions, lead to very high availability of quality-controlled observations: on average, hourly data are available 14 h per day at the grid points around the South Pole and more than 9 h over a large area of the Antarctic Plateau. Processed MODIS land surface temperatures, referred to hereinafter as MODISTs values, were compared with in situ hourly measurements of surface temperature collected over the entirety of the year 2009 by seven stations from the Baseline Surface Radiation Network (BSRN) and automatic weather stations (AWSs). In spite of an occasional failure in the detection of clouds, MODISTs values exhibit a good performance, with a bias ranging from ĝ̂'1.8 to 0.1 °C and errors ranging from 2.2 to 4.8 °C root mean square at the five stations located on the plateau. These results show that MODISTs values can be used as a precise and accurate reference to test other surface temperature data sets. Here, we evaluate the performance of surface temperature in the European Centre for Medium-Range Weather Forecasts (ECMWF) reanalysis known as ERA-Interim reanalysis. During conditions detected as cloud free by MODIS, ERA-Interim shows a widespread warm bias in Antarctica in every season, ranging from +3 to +6 °C on the plateau. This confirms a recent study which showed that the largest discrepancies in 2 m air temperature between ERA-Interim and the global temperature data set HadCRUT4 compiled by the Met Office Hadley Centre and the University of East Anglia's Climatic Research Unit occur in Antarctica. A comparison with in situ surface temperature shows that this bias is not strictly limited to clear-sky conditions. A detailed comparison with stand-alone simula

© 2014 R. Traversi et al. Here we present the first multi-year record of nitrate in the atmospheric aerosol (2005-2008) and surface snow (2006-08) from central Antarctica. PM10 and size-segregated aerosol, together with superficial snow, have been collected all year-round at high resolution (daily for all the snow samples and for most of aerosol samples) at Dome C since the 2004/05 field season and analysed for main and trace ionic markers. The suitability of the sampling location in terms of possible contamination from the base is shown in detail. In spite of the relevance of nitrate in Antarctic atmosphere, both for better understanding the chemistry of N cycle in the plateau boundary layer and for improving the interpretation of long-term nitrate records from deep ice core records, nitrate sources in Antarctica are not well constrained yet, neither in extent nor in timing. A recurring seasonal pattern was pointed out in both aerosol and snow records, showing summer maxima and winter minima, although aerosol maxima lead the snow ones of 1-2 months, possibly due to a higher acidity in the atmosphere in mid-summer, favouring the repartition of nitrate as nitric acid and thus its uptake by the surface snow layers. On the basis of a meteorological analysis of one major nitrate event, of data related to PSC I extent and of irradiance values, we propose that the high nitrate summer levels in aerosol and snow are likely due to a synergy of enhanced source of nitrate and/or its precursors (such as the stratospheric inputs), higher solar irradiance and higher oxidation rates in this season. Moreover, we show here a further evidence of the substantial contribution of HNO3/NOx re-emission from the snowpack, already shown in previous works, and which can explain a significant fraction of atmospheric nitrate, maintaining the same seasonal pattern in the snow. As concerning snow specifically, the presented data suggest that nitrate is likely to be controlled mainly b

Downwelling and upwelling shortwave and longwave radiation components from six active polar sites, taking part of the Baseline Surface Radiation Network (BSRN), were selected for the period of the last International Polar Year (March 2007 to March 2009), and included in the BSRN-IPY dataset, along with metadata and supplementary data for some of the stations. Two sites, located at Svalbard archipelago (Ny Ålesund) and Alaska (Barrow), represent Arctic sea-level conditions. Four Antarctic stations represent both sea-level (Dronning Maud Land and Cosmonaut Sea) and high-elevation conditions (South Pole and East Antarctic Plateau). The BSRN-IPY dataset content and quality are discussed. The dataset is now available at doi:10.1594/PANGAEA.737668, and can be used for free after accepting the BSRN data release guidelines. The dataset has been summarized as monthly averages and subject to further evaluation according to strict criteria not previously applied.