ABSTRACT. Recent snow accumulation rate is a key quantity for ice-core and mass-balance studies. Several accumulation measurement methods (stake farm, fin core, snow-radar profiling, surface morphology, remote sensing) were used, compared and integrated at eight sites along a transect from Terra Nova Bay to Dome C, East Antarctica, to provide information about the spatial and temporal variability of snow accumulation. Thirty-nine cores were dated by identifying tritium/b marker levels (1965-66) and non-sea-salt (nss) SO 4 2-spikes of the Tambora (Indonesia) volcanic event (1816) in order to provide information on temporal variability. Cores were linked by snow radar and global positioning system surveys to provide detailed information on spatial variability in snow accumulation. Stake-farm and ice-core accumulation rates are observed to differ significantly, but isochrones (snow radar) correlate well with ice-core derived accumulation. The accumulation/ablation pattern from stake measurements suggests that the annual local noise (metre scale) in snow accumulation can approach 2 years of ablation and more than four times the average annual accumulation, with no accumulation or ablation for a 5 year period in up to 40% of cases. The spatial variability of snow accumulation at the kilometre scale is one order of magnitude higher than temporal variability at the multi-decadal/secular scale. Stake measurements and firn cores at Dome C confirm an approximate 30% increase in accumulation over the last two centuries, with respect to the average over the last 5000 years.
a b s t r a c tThe EPICA ice core from Dome C extends 3259 m in depth, and encompasses 800 ka of datable and sequential ice. Numerous chemical species have been measured along the length of the cores. Here we concentrate on interpreting the main low-resolution patterns of major ions. We extend the published record for non-sea-salt calcium, sea-salt sodium and non-sea-salt sulfate flux to 800 ka. The non-sea-salt calcium record confirms that terrestrial dust originating from South America closely mirrored Antarctic climate, both at orbital and millennial timescales. A major cause of the main trends is most likely climate in southern South America, which could be sensitive to subtle changes in atmospheric circulation. Seasalt sodium also follows temperature, but with a threshold at low temperature. We re-examine the use of sodium as a sea ice proxy, concluding that it is probably reflecting extent, with high salt concentrations reflecting larger ice extents. With this interpretation, the sodium flux record indicates low ice extent operating as an amplifier in warm interglacials. Non-sea-salt sulfate flux is almost constant along the core, confirming the lack of change in marine productivity (for sulfur-producing organisms) in the areas of the Southern Ocean contributing to the flux at Dome C. For the first time we also present long records of reversible species such as nitrate and chloride, and show that the pattern of post-depositional losses described for shallower ice is maintained in older ice. It appears possible to use these concentrations to constrain snow accumulation rates in interglacial ice at this site, and the results suggest a possible correction to accumulation rates in one early interglacial. Taken together the chemistry records offer a number of constraints on the way the Earth system combined to give the major climate fluctuations of the late Quaternary period.
Abstract. Number
concentrations of ice-nucleating particles (NINP) in the Arctic
were derived from ground-based filter samples. Examined samples had been
collected in Alert (Nunavut, northern Canadian archipelago on Ellesmere
Island), Utqiaġvik, formerly known as Barrow (Alaska), Ny-Ålesund
(Svalbard), and at the Villum Research Station (VRS; northern Greenland). For
the former two stations, examined filters span a full yearly cycle. For VRS,
10 weekly samples, mostly from different months of one year, were included.
Samples from Ny-Ålesund were collected during the months from March until
September of one year. At all four stations, highest concentrations were
found in the summer months from roughly June to September. For those stations
with sufficient data coverage, an annual cycle can be seen. The spectra of
NINP observed at the highest temperatures, i.e., those obtained
for summer months, showed the presence of INPs that nucleate ice up to
−5 ∘C. Although the nature of these highly ice-active INPs could
not be determined in this study, it often has been described in the
literature that ice activity observed at such high temperatures originates
from the presence of ice-active material of biogenic origin. Spectra observed
at the lowest temperatures, i.e., those derived for winter months, were on
the lower end of the respective values from the literature on Arctic INPs or
INPs from midlatitude continental sites, to which a comparison is presented
herein. An analysis concerning the origin of INPs that were ice active at
high temperatures was carried out using back trajectories and satellite
information. Both terrestrial locations in the Arctic and the adjacent sea
were found to be possible source areas for highly active INPs.
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