A Glaciochemical Survey of the Summit Region, Greenland

Spatial representativeness and an understanding of controls on chemical species distribution are essential requirements of any significant ice core investigation. Snowpit studies provide an essential tool in this process. In preparation for the central Greenland deep drilling effort a series of snowpits was sampled in detail for oxygen isotopes, major anions, major cations, total acidity and radionuclides. The results of this sampling program are used to define: (I) the chemical composition of the snow in the region, (2) the input timing and spatial distribution of major chemical species, (3) the potential dependence of species concentration on accumulation rate, and (4) the signal characteristics identifiable in the region over the last few years

Climatic impact of the A.D. 1783 Asama (Japan) Eruption was minimal: Evidence from the GISP2 Ice Core

Assessing the climatic impact of the A.D. 1783 eruption of Mt. Asama, Japan, is complicated by the concurrent eruption of Laki, Iceland. Estimates of the stratospheric loading of H2SO4 for the A.D. 1108 eruption of Asama derived from the SO42− time series in the GISP2 Greenland ice core indicate a loading of about 10.4 Tg H2SO4 with a resulting stratospheric optical depth of 0.087. Assuming sulfur emissions from the 1783 eruption were only one‐third of the 1108 event yields a H2SO4 loading value of 3.5 Tg and a stratospheric optical depth of only 0.029. These results suggest minimal climatic effects in the Northern Hemisphere from the 1783 Asama eruption, thus any volcanically‐induced cooling in the mid‐1780s is probably due to the Laki eruption

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

A High-Altitude Snow Chemistry Record from Amundsenisen, Dronning Maud Land, Antarctica

In this paper a detailed record of major ions from a 20 in deep firn core from Amundsenisen, western Dronning Maud Land, Antarctica, is presented. The core was drilled at 75degreesS, 2degrees 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-, SO42- 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 to Tarawera, 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 Nino-Southern Oscillation events

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

The effect of spatial and temporal accumulation rate variability in west Antarctica on soluble ion deposition

Annually‐dated snowpit and ice core records from two areas of West Antarctica are used to investigate spatial accumulation patterns and to evaluate temporal accumulation rate/glaciochemical concentration and flux relationships. Mean accumulation rate gradients in Marie Byrd Land (11–23 gcm−2yr−1 over 150 km, decreasing to the south) and Siple Dome (10–18 gcm−2yr−1 over 60 km, decreasing to the south) are consistent for at least the last several decades, and demonstrate the influence of the offshore quasi‐permanent Amundsen Sea low pressure system on moisture flux into the region. Local and regional‐scale topography in both regions appears to affect orographic lifting, air mass trajectories, and accumulation distribution. Linear regression of mean annual soluble ion concentration and flux data vs. accumulation rates in both regions indicates that 1) concentrations are independent of and thus not a rescaling of accumulation rate time‐series, and 2) chemical flux to the ice sheet surface is mainly via wet deposition, and changes in atmospheric concentration play a significant role. We therefore suggest that, in the absence of detailed air/snow transfer models, ice core chemical concentration and not flux time‐series provide a better estimate of past aerosol loading in West Antarctica

A Northern Hemisphere Volcanic Chemistry Record (1869-1984) and Climatic Implications using a South Greenland Ice Core

The effect of volcanic emISSIOn of acidic aerosols on climate is well documented. The presence of acid droplets in the stratosphere can reduce transmissivity and hence decrease surface temperatures. Since the amount and chemical composition of erupted material has important effects on regional climate, knowledge of past volcanic events is of extreme importance. Detailed glaciochemical records provide the only milieu wherein the geochemistry of paleovolcanic events can be fully documented. We present a detailed sulfate and chloride record from an ice core drilled at site 20 D, 40 km SW of Dye 3 in southern Greenland. The record spans the time period 1869-1984 with chemical analyses of approximately eight samples per year. Time series decomposition and locally weighted scatter plot smoothing techniques were used to extract long term trends from the data so that individual volcanic eruptions could be documented. A number of events identified here have been unnoticed previously and a high percentage of the major chemical signatures documenting these events is associated with large decreases in temperature in the latitudinal zone 60-90° N. Many authors have pointed out that the amount of volcanic acids such as HCI and H2S04 injected into the atmosphere has a very important influence on global climate, yet this volcanic input has been difficult to quantify prior to ~1960. Our data help to alleviate this problem. These individual events can be compared to available frost tree ring data from North America, further establishing a volcanism—climatic linkage

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

The Dominion Range Ice Core, Queen Maud Mountains, Antarctica - General Site and Core Characteristics with Implications

The Transantarctic Mountains of East Antarctica provide a new milieu for retrieval of ice-core records. We report here on the initial findings from the first of these records, the Dominion Range ice-core record. Sites such as the Dominion Range are valuable for the recovery of records detailing climate change, volcanic activity, and changes in the chemistry of the atmosphere. The unique geographic location of this site and a relatively low accumulation rate combine to provide a relatively long record of change for this potentially sensitive climatic region. As such, information concerning the site and general core characteristics are presented, including ice surface, ice thickness, bore-hole temperature, mean annual net accumulation, crystal size, crystal fabric, oxygen-isotope composition, and examples of ice chemistry and isotopic composition of trapped gases

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\u27 S, 58°50\u27 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 δ18O profile suggests that the principal peaks of methanesulfonate are associated with snow deposited in summer and autumn. A careful examination of MSA, SO42-and nssSO42- profiles indicates that two of the three peaks in the MSA profile mayresult mainlyfrom 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/nssSO42- ratio should be changed. The MSA/nssSO42- ratio obtained bya new computation is 0.22, 10% higher than that ignoring the effect of MSA migration