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Records of chemical impurities from ice cores enable us to reconstruct the past deposition of aerosols onto polar ice sheets and alpine glaciers. Through this they allow us to gain insight into changes of the source, transport and deposition processes that ultimately determine the deposition flux at the coring location. However, the low concentrations of the aerosol species in the ice and the resulting high risk of contamination pose a formidable analytical challenge, especially if long, continuous and highly resolved records are needed. Continuous flow analysis, CFA, the continuous melting, decontamination and analysis of ice-core samples has mostly overcome this issue and has quickly become the de facto standard to obtain high-resolution aerosol records from ice cores after its inception at the University of Bern in the mid-1990s. Here, we present continuous records of calcium (Ca2+), sodium (Na+), ammonium (NH+4), nitrate (NO-3) and electrolytic conductivity at 1 mm depth resolution from the NGRIP (North Greenland Ice Core Project) and NEEM (North Greenland Eemian Ice Drilling) ice cores produced by the Bern Continuous Flow Analysis group in the years 2000 to 2011 (Erhardt et al., 2021). Both of the records were previously used in a number of studies but were never published in full 1 mm resolution. Alongside the 1 mm datasets we provide decadal averages, a detailed description of the methods, relevant references, an assessment of the quality of the data and its usable resolution. Along the way we will also give some historical context on the development of the Bern CFA system.

We introduce an algorithm (called REDFITmc2) for spectrum estimation in the presence of timescale errors. It is based on the Lomb-Scargle periodogram for unevenly spaced time series, in combination with the Welch's Overlapped Segment Averaging procedure, bootstrap bias correction and persistence estimation. The timescale errors are modelled parametrically and included in the simulations for determining (1) the upper levels of the spectrum of the red-noise AR(1) alternative and (2) the uncertainty of the frequency of a spectral peak. Application of REDFITmc2 to ice core and stalagmite records of palaeoclimate allowed a more realistic evaluation of spectral peaks than when ignoring this source of uncertainty. The results support qualitatively the intuition that stronger effects on the spectrum estimate (decreased detectability and increased frequency uncertainty) occur for higher frequencies. The surplus information brought by algorithm REDFITmc2 is that those effects are quantified. Regarding timescale construction, not only the fixpoints, dating errors and the functional form of the age-depth model play a role. Also the joint distribution of all time points (serial correlation, stratigraphic order) determines spectrum estimation.

Continuous sea salt and mineral dust aerosol records have been studied on the two EPICA (European Project for Ice Coring in Antarctica) deep ice cores. The joint use of these records from opposite sides of the East Antarctic plateau allows for an estimate of changes in dust transport and emission intensity as well as for the identification of regional differences in the sea salt aerosol source. The mineral dust flux records at both sites show a strong coherency over the last 150 kyr related to dust emission changes in the glacial Patagonian dust source with three times higher dust fluxes in the Atlantic compared to the Indian Ocean sector of the Southern Ocean (SO). Using a simple conceptual transport model this indicates that transport can explain only 40% of the atmospheric dust concentration changes in Antarctica, while factor 5–10 changes occurred. Accordingly, the main cause for the strong glacial dust flux changes in Antarctica must lie in environmental changes in Patagonia. Dust emissions, hence environmental conditions in Patagonia, were very similar during the last two glacials and interglacials, respectively, despite 2–4 °C warmer temperatures recorded in Antarctica during the penultimate interglacial than today. 2–3 times higher sea salt fluxes found in both ice cores in the glacial compared to the Holocene are difficult to reconcile with a largely unchanged transport intensity and the distant open ocean source. The substantial glacial enhancements in sea salt aerosol fluxes can be readily explained assuming sea ice formation as the main sea salt aerosol source with a significantly larger expansion of (summer) sea ice in the Weddell Sea than in the Indian Ocean sector. During the penultimate interglacial, our sea salt records point to a 50% reduction of winter sea ice coverage compared to the Holocene both in the Indian and Atlantic Ocean sector of the SO. However, from 20 to 80 ka before present sea salt fluxes show only very subdued millennial changes d

Corresponding millennial-scale climate changes have been reported from the North Atlantic region and from east Asia for the last glacial period on independent timescales only. To assess their degree of synchrony we suggest interpreting Greenland ice core dust parameters as proxies for the east Asian monsoon systems. This allows comparing North Atlantic and east Asian climate on the same timescale in high resolution ice core data without relative dating uncertainties. We find that during Dansgaard-Oeschger events North Atlantic region temperature and east Asian storminess were tightly coupled and changed synchronously within 5–10 years with no systematic lead or lag, thus providing instantaneous climatic feedback. The tight link between North Atlantic and east Asian glacial climate could have amplified changes in the northern polar cell to larger scales. We further find evidence for an early onset of a Younger Dryas-like event in continental Asia, which gives evidence for heterogeneous climate change within east Asia during the last deglaciation.

Udgivelsesdato: March 21

Udgivelsesdato: 23 March

A continuous high-resolution record of digital images has been obtained from the North Greenland Ice Core Project (NorthGRIP) ice core (75.1N, 42.3W) in the depth interval from 1330 m to the bedrock at 3085 m. The ice core stratigraphy is clearly visible throughout the glacial period with the most frequent and brightest visible layers appearing during the coldest events. Down to a depth of 2600 m the horizontal layeringis very regular; below this depth, small irregularities in the layering start to appear, and below 2800 m the visual stratigraphy becomes more uncertain, perhaps because of penetration into climatically warmer ice. Comparison of the visual stratigraphy with high-resolution continuous records of chemical impurities and dust reveals a high degree of correlation, which indicates that the visible layers are caused by these impurities. Anew approach is used to automatically determine annual layer thicknesses from the visual stratigraphy record by carrying out a frequency analysis of the most prominent visible layers in the profile. The result gives strong support for the NorthGRIP timescale model.

The timing and synchronisation of Greenland and Antarctic climate events that occurred during the last glacial period are still under debate, as is the magnitude of temperature change associated with these events. Here we present detailed records of local and moisture-source temperature changes spanning the period 27-45 kyr BP from water stable isotope measurements (δD and δ18O) in the recently drilled EPICA Dome C ice core, East Antarctic plateau. Using a simple isotopic model, site (Δ T site) and source (Δ T source) temperatures are extracted from the initial 50-yr high-resolution isotopic records, taking into account the changes in seawater isotopic composition. The deuterium isotope variability is very similar to the less precise δD record from the Vostok ice core, and the site temperature inversion leads to a temperature profile similar to the classical palaeothermometry method, due to compensations between source and ocean water corrections. The reconstructed Δ T site and Δ T source profiles show different trends during the glacial: the former shows a decreasing trend from the warm A1 event (38 kyr BP) toward the Last Glacial Maximum, while the latter shows increasing values from 41 to 28 kyr BP. The low-frequency deuterium excess fluctuations are strongly influenced by obliquity fluctuations, controlling the low- to high-latitude temperature gradients, and show a remarkable similarity with a high-resolution southeast Atlantic sea surface temperature record. A comparison of the temperature profiles (site and source) and temperature gradient (Δ T source-Δ T site) with the non-sea-salt calcium and sodium records suggests a secondary influence of atmospheric transport changes on aerosol variations. © 2003 Elsevier B.V. All rights reserved., SCOPUS: ar.j, info:eu-repo/semantics/published

Chloride (Cl-) and sodium (Na+) in ice cores originate mainly from sea salt, and one would thus expect the Cl-/Na+ ratio to reflect the seawater ratio. However, at Dome C, a low-accumulation site in East Antarctica, this is not the case in present-day snow. Instead, a Cl- excess relative to Na+ is observed in surface snow, and within a few meters depth the Cl- concentration decreases, and the Cl-/Na+ ratio becomes significantly lower than the seawater ratio. Aerosol studies at coastal Antarctic sites have shown that the reaction of sea-salt aerosols with nitric and sulphuric acid leads to the formation of HCl that eventually escapes the sea-salt aerosol. The observed decrease in Cl- concentrations in the uppermost snow layers is due to reemission of HCl from the snow. Postdepositional loss of HCl depends among other factors on the accumulation rate at the site, with lower accumulation rates leading to larger losses. During the Last Glacial Maximum (LGM) the Cl-/Na+ ratio is relatively stable and close to the seawater ratio, despite the even lower accumulation rate during that time. The likely explanation for this conflicting observation is that high levels of dust neutralized nitric and sulphuric acids during the LGM which in turn reduced the formation of HCl from sea-salt aerosol. With less or no HCl formed, postdepositional loss would be prevented, keeping the Cl-/Na+ ratio close to that of sea water.

The sea ice surface, not open water, is the dominant source of sea salt to aerosol and ice cores in coastal Antarctica. Here, we show that it may also form the dominant source for central Antarctica. We can then explain higher concentrations in the winter and last glacial maximum (LGM) as being due to increased sea ice production. This suggests that ice core sea salt can indicate at least the timing of changes in Antarctic sea ice production. The pattern of sea salt in ice cores is consistent with marine evidence about sea ice changes in the Holocene and LGM. Sea salt shows no change at the initial CO2 increase out of the last glacial, making it unlikely this was primarily due to changing sea ice cover. The sea salt record should not be treated as an indicator of meridional transport.

Udgivelsesdato: 30 August

A compilation of nitrate (NO(3)(-)) data from Greenland has shown that recent NO(3)(-) concentrations reveal a temperature dependence similar to that seen in Antarctica. Except for sites with very low accumulation rates, lower temperatures tend to lead to higher NO(3)(-) concentrations preserved in the ice. Accumulation rate, which is closely linked to temperature, might influence the concentrations preserved in snow as well, but its effect cannot be separated from the temperature imprint. Processes involved in NO(3)(-) deposition are discussed and shown to be temperature- and/or accumulation-rate-dependent. Apart from scavenging of nitric acid (HNO(3)) during formation of precipitation, uptake of HNO(3) onto the ice crystal's surface during and after precipitation seems to contribute further to the NO(3)(-) concentrations found in surface snow. Post-depositional loss of NO(3)(-) from the top snow layers is caused by release of HNO(3) and by photolysis of NO(3)(-). It is suggested that photolysis accounts for considerable losses at sites with very low accumulation rates. Depending on the site characteristic, and given that the temperature and accumulation-rate dependence is quantified, it should be possible to infer changes in atmospheric HNO(3) concentrations.

Udgivelsesdato: 1 Feb.

In order to estimate past changes in atmospheric NOx concentration, nitrate, an oxidation product of NOx, has often been measured in polar ice cores. In the frame of the European Project for Ice Coring in Antarctica (EPICA), a high-resolution nitrate record was obtained by continuous flow analysis (CFA) of a new deep ice core drilled at Dome C. This record allows a detailed comparison of nitrate with other chemical trace substances in polar snow under different climatic regimes. Previous studies showed that it would be difficult to make firm conclusions about atmospheric NOx concentrations based on ice core nitrate without a better understanding of the factors controlling NO3− deposition and preservation. At Dome C, initially high nitrate concentrations (over 500 ppb) decrease within the top meter to steady low values around 15 ppb that are maintained throughout the Holocene ice. Much higher concentrations (averaging 53 ppb) are found in ice from the Last Glacial Maximum (LGM). Combining this information with data from previous sampling elsewhere in Antarctica, it seems that under climatic conditions of the Holocene, temperature and accumulation rate are the key factors determining the NO3− concentration in the ice. Furthermore, ice layers with high acidity show a depletion of NO3−, but higher concentrations are found before and after the acidity layer, indicating that NO3− has been redistributed after deposition. Under glacial conditions, where NO3− shows a higher concentration level and also a larger variability, non-sea-salt calcium seems to act as a stabilizer, preventing volatilization of NO3− from the surface snow layers.