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Observations of snow properties, superimposed ice, and atmospheric heat fluxes have been performed on first-year and second-year sea ice in the western Weddell Sea, Antarctica. Snow in this region is particular as it does usually survive summer ablation. Measurements were performed during Ice Station Polarstern (ISPOL), a 5-week drift station of the German icebreaker RV Polarstern. Net heat flux to the snowpack was 8 W m−2, causing only 0.1 to 0.2 m of thinning of both snow cover types, thinner first-year and thicker second-year snow. Snow thinning was dominated by compaction and evaporation, whereas melt was of minor importance and occurred only internally at or close to the surface. Characteristic differences between snow on first-year and second-year ice were found in snow thickness, temperature, and stratigraphy. Snow on second-year ice was thicker, colder, denser, and more layered than on first-year ice. Metamorphism and ablation, and thus mass balance, were similar between both regimes, because they depend more on surface heat fluxes and less on underground properties. Ice freeboard was mostly negative, but flooding occurred mainly on first-year ice. Snow and ice interface temperature did not reach the melting point during the observation period. Nevertheless, formation of discontinuous superimposed ice was observed. Color tracer experiments suggest considerable meltwater percolation within the snow, despite below-melting temperatures of lower layers. Strong meridional gradients of snow and sea-ice properties were found in this region. They suggest similar gradients in atmospheric and oceanographic conditions and implicate their importance for melt processes and the location of the summer ice edge.

Firn air was sampled on the Antarctic plateau in Dronning Maud Land (DML), during the Norwegian Antarctic Research Expedition (NARE) 2000/2001. In this paper, we describe the analyses for methyl chloride and nonmethane hydrocarbons (NMHCs) in these firn air samples. For the first time, the NMHCs ethane, propane, and acetylene have been measured in Antarctic firn air, and concentration profiles for these gases have been derived. A one-dimensional numerical firn air diffusion model was used to interpret the measured profiles and to derive atmospheric concentrations as a function of time. The atmospheric trends we derived for the NMHC and methyl chloride at DML cover the period from 1975 to 2000. Methyl chloride shows a decreasing trend of 1.2 ± 0.6 ppt per year (annual mean concentration 548 ± 32 ppt). For ethane we found an increasing trend of 1.6 ± 0.6 ppt per year (annual mean concentration 241 ± 12 ppt). The concentrations of propane and acetylene appear to be constant over the period 1975–2000, with annual mean concentrations of 30 ± 4 ppt for propane and 24 ± 2 ppt for acetylene.

This paper presents atmospheric concentrations of ethane, propane, acetylene, and methyl chloride, inferred from firn air by using a numerical one-dimensional firn diffusion model. The firn air was collected on the Antarctic plateau in Dronning Maud Land during the Norwegian Antarctic Research Expedition (NARE) 2000/2001. The influences of seasonal variations in temperature and pressure and the variation in accumulation rate were studied and are not negligible, but appear to cancel each other out if all variability is taken into account. This paper also demonstrates that firn air from the uppermost firn layer (30 m) can be used to derive seasonal cycles of these trace gases, without needing a year-round facility. These cycles display higher atmospheric mixing ratios during the Antarctic winter and lower atmospheric mixing ratios in summer. The cycles for the year 2000 show amplitudes of 140 ± 25 ppt for ethane, 30 ± 10 ppt for propane, 24 ± 6 ppt for acetylene, and 40 ± 20 ppt for methyl chloride. For ethane and propane the amplitudes and months of maximum atmospheric concentration (phase) are in reasonable agreement with year-round measurements at the South Pole and Baring Head (New Zealand). The amplitudes for methyl chloride and acetylene are significantly greater than seen in year-round measurements at the South Pole and at Neumayer (Antarctica), although the phase is in line. While biomass burning and removal by OH radicals can partially explain these large amplitudes, the exact cause still remains unclear for methyl chloride and acetylene.

Ground-based zenith sky UV–visible measurements of stratospheric bromine monoxide (BrO) slant column densities are compared with simulations from the SLIMCAT three-dimensional chemical transport model. The observations have been obtained from a network of 11 sites, covering high and midlatitudes of both hemispheres. This data set gives for the first time a near-global picture of the distribution of stratospheric BrO from ground-based observations and is used to test our current understanding of stratospheric bromine chemistry. In order to allow a direct comparison between observations and model calculations, a radiative transfer model has been coupled to the chemical model to calculate simulated slant column densities. The model reproduces the observations in general very well. The absolute amount of the BrO slant columns is consistent with a total stratospheric bromine loading of 20 ± 4 ppt for the period 1998–2000, in agreement with previous estimates. The seasonal and latitudinal variations of BrO are well reproduced by the model. In particular, the good agreement between the observed and modeled diurnal variation provides strong evidence that the BrO-related bromine chemistry is correctly modeled. A discrepancy between observed and modeled BrO at high latitudes during events of chlorine activation can be resolved by increasing the rate constant for the reaction BrO + ClO → BrCl + O2 to the upper limit of current recommendations. However, other possible causes of the discrepancy at high latitudes cannot be ruled out.

A number of campaigns have been conducted in order to study Polar Mesosphere Summer Echos (PMSE) and Noctilucent Clouds (NLC) in the period 1991–1994. Several sounding rockets have been launched through these layers with measurements being performed on upleg as well as downleg. These include measurements of positive ions and electrons in both ram and wake positions, as well as measurements of charged aerosols in ram on upleg. In this paper we will review these measurements and make a preliminary classification of the data based upon the presence of PMSE and/or NLC. One of the mechanisms responsible for PMSE is the presence of neutral air turbulence in combination with a high Schmidt number. We will briefly discuss this type of echo using in situ rocket data. Differences and similarities of PMSE and NLC as observed both in the Arctic and the Antarctic will be discussed. Observations show that especially PMSE are much more frequent in the Arctic. This may be due to a difference in the water vapour content or the temperature at mesopause heights. Lack of data in the Antarctic makes it difficult to decide which of these two factors are the most important. More measurements, especially co-ordinated in situ and ground-based lidar and radar measurements, are needed to discuss the Arctic and Antarctic similarities and differences in further detail.

Levels of persistent organic pollutants (POPs), such as polychlorinated biphenyls and pesticides have been determined in ambient air at Signy Island, Antarctica, over a period of 17 weeks. Mean concentrations for single polychlorinated biphenyls (0.02–17 pg/m3), for chlordanes (0.04–0.9 pg/m3), DDT compounds (0.07–0.40 pg/m3) and γ-hexachlorocyclohexane (HCH, 22 pg/m3) were comparable to those in Arctic air. However, α-HCH levels were approximately one order of magnitude lower. Compared to the Arctic, differences were also observed in the concentration ratios of α-/γ-HCH and chlordane compounds. Two possible atmospheric long-range transport episodes from South America were found by comparing 10-day back trajectories with observed concentration changes. The lower limits of determination (LOD) were mainly governed by the field blanks. They were satisfactory for the most volatile PCBs. However, many concentrations for DDT and chlordane compounds were below the LODs (range 0.1–1 pg/m3) or even the instrumental detection limit (0.01–0.03 pg/m3).

In this paper we use output of a high-resolution general circulation model (ECHAM-3 T106, resolution 1.1°?1.1°) to study the spatial and temporal variation of sublimation on Antarctica. First, we compare model results with available observations of sublimation rates. The yearly cycle, with small latent heat fluxes during the winter, is well reproduced, and the agreement with sparsely available spot observations is fair. The model results suggest that a significant 10?15% of the annual precipitation over Antarctica is lost through sublimation and that sublimation plays an important role in the formation of blue ice areas. A preliminary analysis of the atmospheric boundary layer moisture budget shows that the spatial variation of sublimation in the coastal zone of East Antarctica can be explained by variations of horizontal advection of dry air. Dry air advection, and thus surface sublimation, is enhanced in areas where katabatic winds are strong and have a large downslope component and where the Antarctic topography drops suddenly from the plateau to the coastal zone. In areas where horizontal advection is small, like the plateau and the large ice shelves, special conditions must be met to make significant sublimation at the surface possible.