The spatial variation of Asian dust and marine aerosol contributions to glaciochemical signals in central Asia

Short-term (6 months to 17 years) glaciochemical records have been collected from several glacier basins in the mountains of central Asia. The spatial distribution of snow chemistry in central Asia is controlled by the influx of dust from the large expanse of arid and semiarid regions in central Asia. Glaciers in the Northern and Western Tibetan Plateau show elevated concentrations and elevated annual fluxes of calcium, sodium, chloride, sulphate and nitrate due to the influx of desert dust from nearby arid and semi-arid regions. Glaciers in the Southeastern Tibetan Plateau show lower concentrations and lower annual fluxes of major ions due to longer transport distances of dust from the arid and semi-arid regions of Western China. Snow from the Karakoram and Western Himalaya show ion concentrations similar to those in Southeastern Tibetan Plateau, but much higher annual fluxes suggesting that much of the aerosol and moisture transported with the westerly jet stream is removed as it ascends the Southwest margin of the Tibetan Plateau. Snow from the Southern slopes of the Eastern Himalayas shows very low concentrations and very low annual fluxes of major ions, indicating that this region is relatively free from the chemical influence of Asian dust. The glaciochemical data suggest that glaciers which are removed from large source areas of mineral aerosol, such as those in the Himalaya, the Karakoram, and the Southeastern Tibetan Plateau, are the ones most likely to contain longer-term glaciochemical records which detail annual to decadal variation in the strength of the Asian monsoon and long-range transport of Asian dust

A review of Central Asian glaciochemical data

The glaciers of central Asia provide suitable locations from which to recover continuous, high-resolution glaciochemical records on a continental scale. Although the glaciochemical investigations undertaken to date in central Asia are few in number and limited in terms of spatial coverage and length of record, some preliminary observations can be made concerning regional and seasonal trends in snow chemistry in this region. The sodium chloride ratio for most snow samples collected in central Asia approaches the ratio found in sea water (0.86 in /Leq kg-I ), reflecting a marine source for these constituents. Sodium and chloride concentrations are, on average, 3-10 times higher in the Himalayas than in the Karakoram, demonstrating the greater influence of monsoonal sources of moisture in the Himalayas. Very high sodium concentrations from Khel Khod Glacier probably reflect a local crustal source from surrounding ice-free areas. Low nitrate concentrations were found in snow collected from the southern margin of the Himalayas and high concentrations in snow deposited on the north margin of the Himalayas. This strong regional trend in the spatial distribution of nitrate suggests the influx of continental aerosols, rich in nitrate, originating from the arid regions of central Asia. High calcium concentrations measured in snow from Mount Everest and the north-west corner of China are also indicative of dust derived from the arid regions of central Asia. Very high sulfate concentrations found in snow from the Tien Shan and the Bogda Shan most likely reflect local anthropogenic sources. The altitude effect on isotopic composition is not apparent from snow samples collected in central Asia. Understanding the processes which control the chemical content of snow, the local-to-regional scale complexities, and the seasonal variability are fundamental steps necessary to assess the potential for recovering representative long-term glaciochemical records from central Asia

A 200-year 210Pb record from Greenland

A continuous profile of 210Pb activity extending back to 1766 has been developed for a firn/ice core collected at Site D in central Greenland in 1984. Unexpectedly high activities of 210Pb were found at the base of this core (0.032 pCi kg−1 in samples more than 200 years old), calling into question the common assumption that supported 210Pb can be neglected when constructing chronologies in glacial snow and ice. It is problematic to assert that all of the 210Pb measured at depth should be attributed to the supported fraction, given previous estimates of dust loading in Greenland ice cores. However, even if an estimated constant value of 0.032 pCi supported210Pb kg−1 is subtracted from the measured values to estimate excess 210Pb, the 210Pb chronology for Site D yields ages that are significantly younger (mean accumulation rate too high) than an independent depth-age scale based on annual layer counting. It is apparent that the flux of excess and/or supported 210Pb to this site must have decreased over the past 2 centuries, with decreasing trends in both fractions most likely. Previously published 210Pb profiles for cores from Summit and Dye 3, Greenland, show similar trends, which had been interpreted as decreasing fluxes of excess 210Pb only. For all three sites, it is not possible to separate variations in the fluxes of the excess and supported fractions of 210Pb, but variations in the total 210Pb flux will impact 210Pb-based chronologies generally if these variations have not been restricted to the Greenland ice sheet

Spatial variability of climate and past atmospheric circulation patterns from central West Antarctic glaciochemistry

Atmospheric circulation patterns and the spatial variability of atmospheric chemistry and moisture transport in central West Antarctica are investigated using new 40 year long (1954–1994 A.D.) glaciochemical and accumulation rate records developed from four firn cores from this region. The core sites lie on a 200 km traverse from 82° 22′ S, 119° 17′ W to 81° 22′ S, 107° 17′ W. The glaciochemical records represent the major ionic species present in Antarctic snow: Na+, K+, Mg2+, Ca2+, Cl−, NO3−, and SO42−. High spatial variability appears in comparisons of full record averages and poor intersite linear correlation results. Accumulation rates show 50–100% changes over distances of 50–100 km and sea‐salt concentrations drop by 50% between the middle two sites. One likely contributor to the high variability seen at this spatial scale is variability in synoptic‐ and finer‐scale meteorology. Empirical orthogonal function (EOF) analysis shows that 80% or more of the variance in site chemistry can be attributed to two types of air masses: winter season air (50–70% of site variance) with a strong marine signature (heavy loading of sea‐salt species) and summer season air (21% of the variance), marked by marine biogenic non‐sea‐salt SO4 plus NO3. This pattern of winter and summer regimes appears at other West Antarctic sites suggesting it may apply to the entire region. We show that a general picture of the patterns of variability in West Antarctica can best be drawn by using an analysis technique that fully exploits high resolution, multiparameter, multisite data sets

A high-altitude snow chemistry record from Amundsenisen, Dronning Maud Land, Antarctica

In this paper a detailed record of major ions from a 20 m deep firn core from Amundsenisen, western Dronning Maud Land, Antarctica, is presented. The core was drilled at 75° S, 2° E (2900 m a.s.l.) during austral summer 1991/92. The following ions were measured at 3 cm resolution: Na+, Mg2+, Ca2+, Cl−, NO3−, S04 2− and CH3SO3H (MSA). The core was dated back to 1865 using a combination of chemical records and volcanic reference horizons. The volcanic eruptions identified in this core are Mount Ngauruhoe, New Zealand (1974–75), Mount Agung, Indonesia (1963), Azul, Argentina (1932), and a broad peak that corresponds in time toTarawera, New Zealand (1886), Falcon Island, South Shetlands, Southern Ocean (1885), and Krakatau, Indonesia (1883). There are no trends in any of the ion records, but the annual to decadal changes are large. The mean concentrations of the measured ions are in agreement with those from other high-altitude cores from the Antarctic plateau. At this core site there may be a correspondence between peaks in the MSA record and major El Niño–Southern Oscillation events

Chemical species spatial distribution and relationship to elevation and snow accumulation rate over the Greenland Ice Sheet

Major chemical species (Cl−, NO−3, SO2−4, Na+, K+, Mg2+, Ca2+) from 24 snowpits (sampled at a resolution of 3 cm, total 2995 samples) collected from northern, central, and southern Greenland were used for this investigation. The annual and seasonal (winter and summer) concentration of each chemical species was calculated and used to study the spatial distribution of chemical species over the central portion of the Greenland Ice Sheet. A two‐sided t‐distribution test (α = 0.05) suggests that concentrations of major chemical species in snow do not vary significantly over this portion of central Greenland. The relationship between chemical concentration and snow accumulation rate was investigated using annual data from two groups of snowpits: those from coastal sites (northern and southern Greenland); and those from high‐altitude inland sites (central Greenland). The snowpit data from a single group, when examined independently of the other group, show that chemical concentrations do not vary with snow accumulation rate. However, when data from the two groups are integrated into a single data set, pseudorelationships appear, with NO−3 concentration decreasing and Na+, K+, Mg2+, and Cl− increasing as snow accumulation rate increases. Therefore we suggest that it is improper to study the relationship between chemical concentration and snow accumulation rate by using data collected from different geographic sites. The relationship between elevation and chemical concentration was investigated using the same suite of annual data sets. We find that Cl−, Na+, and Mg2+ concentrations decrease, while NO−3 concentration increases, with increasing elevation on the Greenland Ice Sheet

Methanesulfonate in the firn of King George Island, Antarctica

Methanesulfonate was investigated as a potential contributor to the sulfur budget, based on analysis of a firn core from Collins Ice Cap, King George Island, Antarctica (62°10′ S, 58°50′ W). The anion was found to be present at a mean concentration of 0.17 μeq L−1, with a maximum of 0.73 μeq L−1. Dating based on the δ 18O profile suggests that the principal peaks of methanesulfonate are associated with snow deposited in summer and autumn. A careful examination of MSA, SO4 2− and nssSO4 2− profiles indicates that two of the three peaks in the MSA profile may result mainly from migration and relocation of MSA. The mechanism responsible for this might be similar to that for deep cores from other Antarctic glaciers, supporting the migration hypothesis proposed by prior researchers and extending it to near-temperate ice. Due to the post-depositional modification, the main part of the MSA profile of the firn is no longer indicative of the seasonal pattern of MSA in the atmosphere, and the basis for calculation of the MSA/nssSO4 2− ratio should be changed. The MSA/nssS04 2 ratio obtained by a new computation is 0.22, 10% higher than that ignoring the effect of MSA migration

A 110,000‐year history of change in continental biogenic emissions and related atmospheric circulation inferred from the Greenland Ice Sheet Project Ice Core

The 110,000‐year record of ammonium concentrations from the Greenland Ice Sheet Project 2 (GISP2) ice core provides the basis for an analysis of terrestrial biological production and atmospheric circulation patterns involved in the transport of biologically produced ammonium to the Greenland atmosphere. The directly measured concentration series was selected for analysis, rather than that of estimated ammonium flux, after a detailed analysis of the relationship among ice core glaciochemical concentrations and a high‐resolution simultaneous record of snow accumulation from the GISP2 core. Analysis of the ammonium concentration series shows that maxima in background levels of ammonium in the Greenland atmosphere are strongly related to and synchronous with summer forcing associated with the precessional cycle of insolation. Minima in background levels, on the other hand, are delayed relative to minima in summer insolation at those times when ice volume is significant. The duration of these delays are similar in magnitude (≈6000 years) to other paleoclimatic responses to changes in ice volume. Decadal and centennial scale variation about background levels of ammonium concentration exhibit two modes of behavior when compared to a record of polar atmospheric circulation intensity. During warmer periods ammonium transport to Greenland is similar to present patterns. Under coldest conditions the low levels of ammonium transported to Greenland are the result of extreme southerly excursions of the predominantly zonal polar circulation. The rapid transitions (≈200 years) between these two climatic conditions appear to be associated with a critical volume or extent of the continental ice sheets

Potential atmospheric impact of the Toba Mega‐Eruption ∼71,000 years ago

An ∼6‐year long period of volcanic sulfate recorded in the GISP2 ice core about 71,100 ± 5000 years ago may provide detailed information on the atmospheric and climatic impact of the Toba mega‐eruption. Deposition of these aerosols occur at the beginning of an ∼1000‐year long stadial event, but not immediately before the longer glacial period beginning ∼67,500 years ago. Total stratospheric loading estimates over this ∼6‐year period range from 2200 to 4400 Mt of H2SO4 aerosols. The range in values is given to compensate for uncertainties in aerosol transport. Magnitude and longevity of the atmospheric loading may have led directly to enhanced cooling during the initial two centuries of this ∼1000‐year cooling event