scholarly journals Methanesulphonic acid movement in solid ice cores

2004 ◽  
Vol 39 ◽  
pp. 540-544 ◽  
Author(s):  
Barbara T. Smith ◽  
Tas D. Van Ommen ◽  
Mark A. J. Curran

AbstractMethanesulphonic acid (MSA) is an important trace-ion constituent in ice cores, with connections to biological activity and sea-ice distribution. Post-depositional movement of MSA has been documented in firn, and this study investigates movement in solid ice by measuring variations in MSA distribution across several horizontal sections from an ice core after 14.5 years storage. The core used is from below the bubble close-off depth at Dome Summit South, Law Dome, East Antarctica. MSA concentration was studied at 3 and 0.5 cm resolution across the core widths. Its distribution was uniform through the core centres, but the outer 3 cm showed gradients in concentrations down to less than half of the central value at the core edge. This effect is consistent with diffusion to the surrounding air during its 14.5 year storage. The diffusion coefficient is calculated to be 2 ×10–13 m2 s–1, and the implications for the diffusion mechanism are discussed.

2019 ◽  
Vol 116 (10) ◽  
pp. 4099-4104 ◽  
Author(s):  
Louise C. Sime ◽  
Peter O. Hopcroft ◽  
Rachael H. Rhodes

Greenland ice cores provide excellent evidence of past abrupt climate changes. However, there is no universally accepted theory of how and why these Dansgaard–Oeschger (DO) events occur. Several mechanisms have been proposed to explain DO events, including sea ice, ice shelf buildup, ice sheets, atmospheric circulation, and meltwater changes. DO event temperature reconstructions depend on the stable water isotope (δ18O) and nitrogen isotope measurements from Greenland ice cores: interpretation of these measurements holds the key to understanding the nature of DO events. Here, we demonstrate the primary importance of sea ice as a control on Greenland ice coreδ18O: 95% of the variability inδ18O in southern Greenland is explained by DO event sea ice changes. Our suite of DO events, simulated using a general circulation model, accurately captures the amplitude ofδ18O enrichment during the abrupt DO event onsets. Simulated geographical variability is broadly consistent with available ice core evidence. We find an hitherto unknown sensitivity of theδ18O paleothermometer to the magnitude of DO event temperature increase: the change inδ18O per Kelvin temperature increase reduces with DO event amplitude. We show that this effect is controlled by precipitation seasonality.


2021 ◽  
Author(s):  
Pete D. Akers ◽  
Joël Savarino ◽  
Nicolas Caillon ◽  
Mark Curran ◽  
Tas Van Ommen

<p>Precise Antarctic snow accumulation estimates are needed to understand past and future changes in global sea levels, but standard reconstructions using water isotopes suffer from competing isotopic effects external to accumulation. We present here an alternative accumulation proxy based on the post-depositional photolytic fractionation of nitrogen isotopes (d<sup>15</sup>N) in nitrate. On the high plateau of East Antarctica, sunlight penetrating the uppermost snow layers converts snow-borne nitrate into nitrogen oxide gas that can be lost to the atmosphere. This nitrate loss favors <sup>14</sup>NO<sub>3</sub><sup>-</sup> over <sup>15</sup>NO<sub>3</sub><sup>-</sup>, and thus the d<sup>15</sup>N of nitrate remaining in the snow will steadily increase until the nitrate is eventually buried beneath the reach of light. Because the duration of time until burial is dependent upon the rate of net snow accumulation, sites with lower accumulation rates have a longer burial wait and thus higher d<sup>15</sup>N values. A linear relationship (r<sup>2</sup> = 0.86) between d<sup>15</sup>N and net accumulation<sup>-1</sup> is calculated from over 120 samples representing 105 sites spanning East Antarctica. These sites largely encompass the full range of snow accumulation rates observed in East Antarctica, from 25 kg m-<sup>2</sup> yr<sup>-1</sup> at deep interior sites to >400 kg m-<sup>2</sup> yr<sup>-1</sup> at near coastal sites. We apply this relationship as a transfer function to an Aurora Basin ice core to produce a 700-year record of accumulation changes. Our nitrate-based estimate compares very well with a parallel reconstruction for Aurora Basin that uses volcanic horizons and ice-penetrating radar. Continued improvements to our database may enable precise independent estimates of millennial-scale accumulation changes using deep ice cores such as EPICA Dome C and Beyond EPICA-Oldest Ice.</p>


2016 ◽  
Vol 62 (236) ◽  
pp. 1037-1048 ◽  
Author(s):  
F. PARRENIN ◽  
S. FUJITA ◽  
A. ABE-OUCHI ◽  
K. KAWAMURA ◽  
V. MASSON-DELMOTTE ◽  
...  

ABSTRACTDocumenting past changes in the East Antarctic surface mass balance is important to improve ice core chronologies and to constrain the ice-sheet contribution to global mean sea-level change. Here we reconstruct past changes in the ratio of surface mass balance (SMB ratio) between the EPICA Dome C (EDC) and Dome Fuji (DF) East Antarctica ice core sites, based on a precise volcanic synchronization of the two ice cores and on corrections for the vertical thinning of layers. During the past 216 000 a, this SMB ratio, denoted SMBEDC/SMBDF, varied between 0.7 and 1.1, being small during cold periods and large during warm periods. Our results therefore reveal larger amplitudes of changes in SMB at EDC compared with DF, consistent with previous results showing larger amplitudes of changes in water stable isotopes and estimated surface temperature at EDC compared with DF. Within the last glacial inception (Marine Isotope Stages, MIS-5c and MIS-5d), the SMB ratio deviates by up to 0.2 from what is expected based on differences in water stable isotope records. Moreover, the SMB ratio is constant throughout the late parts of the current and last interglacial periods, despite contrasting isotopic trends.


2021 ◽  
Author(s):  
Theo Jenk ◽  
Daniela Festi ◽  
Margit Schwikowski ◽  
Valter Maggi ◽  
Klaus Oeggl

<p>Dating glaciers is an arduous yet essential task in ice core studies, which becomes even more challenging for the dating of glaciers suffering from mass loss in the accumulation zone as result of climate warming. In this context, we present the dating of a 46 m deep ice core from the Central Italian Alps retrieved in 2016 from the Adamello glacier (Pian di Neve, 3100 m a.s.l.). We will show how the timescale for the core could be obtained by integrating results from the analyses of the radionuclides <sup>210</sup>Pb and <sup>137</sup>Cs with annual layer counting derived from pollen and refractory black carbon concentrations. Our results clearly indicate that the surface of the glacier is older than the drilling date of 2016 by about 20 years and that the 46 m ice core reaches back to around 1944. Despite the severe mass loss affecting this glacier even in the accumulation zone, we show that it is possible to obtain a reliable timescale for such a temperate glacier. These results are very encouraging and open new perspectives on the potential of such glaciers as informative palaeoarchives. We thus consider it important to present our dating approach to a broader audience.</p>


1991 ◽  
Vol 37 (127) ◽  
pp. 357-367
Author(s):  
J.-L. Tison ◽  
E. M. Morris ◽  
R. Souchez ◽  
J. Jouzel

AbstractResults from a detailed profile in a 5.54 m multi-year sea-ice core from the rift area in the southern part of George VI Ice Shelf are presented. Stratigraphy, stable isotopes and Na content are used to investigate the growth processes of the ice cover and to relate them to melting processes at the bottom of the ice shelf.The thickest multi-year sea ice in the sampling area appears to be second-year sea ice that has survived one melt season. Combined salinity/stable-isotope analyses show large-scale sympathetic fluctuations that can be related to the origin of the parent water. Winter accretion represents half of the core length and mainly consists of frazil ice of normal sea-water origin. However, five major dilution events of sea water, with fresh-water input from the melting base of the ice shelf reaching 20% on two occasions, punctuate this winter accretion. Two of them correspond to platelet-ice production, which is often related to the freezing of ascending supercooled water from the bottom of the ice shelf.Brackish ice occurs between 450 and 530 cm in the core. It is demonstrated that this results from the freezing of brackish water (Jeffries and others, 1989) formed by mixing of normal sea water with melted basal shelf ice, with dilution percentages of maximum 80% fresh water.


1994 ◽  
Vol 40 (136) ◽  
pp. 504-508 ◽  
Author(s):  
Michael Ram ◽  
Matthias Illing

Abstract We describe a new laser-light-scattering instrument for measuring variations in dust concentration along polar ice cores. We have used this instrument with considerable success on the GISP2 ice core from central Greenland. Reproducibility is excellent and the required ice-sample size is relatively small. When combined with visual stratigraphy and ECM, the distinct annual spring/ summer dust peaks we observe can be used to date the core with tree-ring-like precision.


2013 ◽  
Vol 9 (6) ◽  
pp. 2789-2807 ◽  
Author(s):  
S. Schüpbach ◽  
U. Federer ◽  
P. R. Kaufmann ◽  
S. Albani ◽  
C. Barbante ◽  
...  

Abstract. In this study we report on new non-sea salt calcium (nssCa2+, mineral dust proxy) and sea salt sodium (ssNa+, sea ice proxy) records along the East Antarctic Talos Dome deep ice core in centennial resolution reaching back 150 thousand years (ka) before present. During glacial conditions nssCa2+ fluxes in Talos Dome are strongly related to temperature as has been observed before in other deep Antarctic ice core records, and has been associated with synchronous changes in the main source region (southern South America) during climate variations in the last glacial. However, during warmer climate conditions Talos Dome mineral dust input is clearly elevated compared to other records mainly due to the contribution of additional local dust sources in the Ross Sea area. Based on a simple transport model, we compare nssCa2+ fluxes of different East Antarctic ice cores. From this multi-site comparison we conclude that changes in transport efficiency or atmospheric lifetime of dust particles do have a minor effect compared to source strength changes on the large-scale concentration changes observed in Antarctic ice cores during climate variations of the past 150 ka. Our transport model applied on ice core data is further validated by climate model data. The availability of multiple East Antarctic nssCa2+ records also allows for a revision of a former estimate on the atmospheric CO2 sensitivity to reduced dust induced iron fertilisation in the Southern Ocean during the transition from the Last Glacial Maximum to the Holocene (T1). While a former estimate based on the EPICA Dome C (EDC) record only suggested 20 ppm, we find that reduced dust induced iron fertilisation in the Southern Ocean may be responsible for up to 40 ppm of the total atmospheric CO2 increase during T1. During the last interglacial, ssNa+ levels of EDC and EPICA Dronning Maud Land (EDML) are only half of the Holocene levels, in line with higher temperatures during that period, indicating much reduced sea ice extent in the Atlantic as well as the Indian Ocean sector of the Southern Ocean. In contrast, Holocene ssNa+ flux in Talos Dome is about the same as during the last interglacial, indicating that there was similar ice cover present in the Ross Sea area during MIS 5.5 as during the Holocene.


1990 ◽  
Vol 14 ◽  
pp. 350
Author(s):  
R. Mulvaney ◽  
A.P. Reid ◽  
D A. Peel

A continuous, detailed, 200-years record of the anionic species, chloride, nitrate and sulphate, has been measured on an ice core from Dolleman Island (70°35.2′ S, 60°55.5′ W), Antarctic Peninsula. The site lies on the east coast of the Peninsula, and the chemistry of the core is dominated by the changing pattern of sea-ice distribution and storm activity in the Wed dell Sea. Strong annual cycles in chloride and non sea salt sulphate reflect the dominance of the seasonal cycle in sea-ice distribution in the Weddell Sea, observed in time series derived from satellite imagery since the early 1970s. However, in the case of chloride there is also an exceptionally strong interannual variability, which in many parts of the core dominates the seasonal cycle. Secular variations in the sea-ice extent appear to have a strong influence on the climate of the region and may play a major role in determining how long-term climate change in the Antarctic Peninsula relates to global climate change. The paper examines documented evidence for sea-ice extent in the Weddell Sea sector, and evaluates the usefulness of ice-core data for reconstructing this parameter in the earlier period.


2011 ◽  
Vol 52 (57) ◽  
pp. 347-354 ◽  
Author(s):  
Sharon B. Sneed ◽  
Paul A. Mayewski ◽  
Daniel A. Dixon

AbstractUsing results stemming from the International Trans-Antarctic Scientific Expedition (ITASE) ice-core array plus data from ice cores from the South Pole and Siple Dome we investigate the use of sodium (Na+), non-sea-salt sulfate (nssSO42–) and methylsulfonate (MS–) as proxies for Antarctic sea-ice extent (SIE). Maximum and mean annual chemistry concentrations for these three species correlate significantly with maximum, mean and minimum annual SIE, offering more information and clarification than single ice-core and single species approaches. Significant correlations greater than 90% exist between Na+ and maximum SIE; nssSO42– with minimum and mean SIE; and MS– with mean SIE. Correlations with SIE within large geographic regions are in the same direction for all ice-core sites for Na+ and nssSO42– but not MS–. All ice cores display an SIE correlation with nssSO42– and MS–, but not all correlate with Na+. This multi-core multi-parameter study provides the initial step in determining which chemical species can be used reliably and in which regions as a building block for embedding other ice-core records. Once established, the resulting temporal and spatial matrix can be used to relate ice extents, atmospheric patterns, biological productivity and site conditions.


2009 ◽  
Vol 55 (193) ◽  
pp. 784-788 ◽  
Author(s):  
Jason L. Roberts ◽  
Tas D. Van Ommen ◽  
Mark A.J. Curran ◽  
Tessa R. Vance

AbstractThe loss of methanesul phonic acid (MSA) from stored ice cores can be significant over typical storage times, with diffusion to the ice-core surface controlling the loss. Methods for minimizing this loss are discussed and it is shown how measurements can be corrected by calculating the amount of MSA lost. A revised diffusion coefficient for MSA in solid ice, (4.1 × 10−13) ± (2.5 × 10−14) m2 s−1, is derived to improve such MSA loss corrections.


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