ALBERT

Description: We study a firn and ice core drilled at the new “Lock-In” site in East Antarctica, located 136 km away from Concordia station towards Dumont d'Urville. High-resolution chemical and physical measurements were performed on the core, with a particular focus on the trapping zone of the firn where air bubbles are formed. We measured the air content in the ice, closed and open porous volumes in the firn, firn density, firn liquid conductivity, major ion concentrations, and methane concentrations in the ice. The closed and open porosity volumes of firn samples were obtained using the two independent methods of pycnometry and tomography, which yield similar results. The measured increase in the closed porosity with density is used to estimate the air content trapped in the ice with the aid of a simple gas-trapping model. Results show a discrepancy, with the model trapping too much air. Experimental errors have been considered but do not explain the discrepancy between the model and the observations. The model and data can be reconciled with the introduction of a reduced compression of the closed porosity compared to the open porosity. Yet, it is not clear if this limited compression of closed pores is the actual mechanism responsible for the low amount of air in the ice. High-resolution density measurements reveal the presence of strong layering, manifesting itself as centimeter-scale variations. Despite this heterogeneous stratification, all layers, including the ones that are especially dense or less dense compared to their surroundings, display similar pore morphology and closed porosity as a function of density. This implies that all layers close in a similar way, even though some close in advance or later compared to the bulk firn. Investigation of the chemistry data suggests that in the trapping zone, the observed stratification is partly related to the presence of chemical impurities.

Description: In order to interpret the paleoclimatic record stored in the air enclosed in polar ice cores, it is crucial to understand the fundamental lock-in process. Within the porous firn, bubbles are sealed continuously until the respective horizontal layer reaches a critical porosity. Present-day firn air models use a postulated temperature dependence of this value as the only parameter to adjust to the surrounding conditions of individual sites. However, no direct measurements of the firn microstructure could confirm these assumptions. Here we show that the critical porosity is a climate-independent constant by providing an extensive data set of micrometer-resolution 3-D X-ray computer tomographic measurements for ice cores representing different extremes of the temperature and accumulation ranges. We demonstrate why indirect measurements suggest a climatic dependence and substantiate our observations by applying percolation theory as a theoretical framework for bubble trapping. The incorporation of our results significantly influences the dating of trace gas records, changing gas-age–ice-age differences by up to more than 1000 years. This may further help resolve inconsistencies, such as differences between East Antarctic δ15N records (as a proxy for firn height) and model results. We expect our findings to be the basis for improved firn air and densification models, leading to lower dating uncertainties. The reduced coupling of proxies and surrounding conditions may allow for more sophisticated reinterpretations of trace gas records in terms of paleoclimatic changes and will benefit the development of new proxies, such as the air content as a marker of local insolation.

Description: We study a firn and ice core drilled at the new "Lock-In" site in East Antarctica, located 136 km away from Concordia station towards Durmont d'Urville. High resolution chemical and physical measurements were performed on the core, with a particular focus on the trapping zone of the firn where air bubbles are formed. We measured the air content in the ice, closed and open porous volumes in the firn, firn density, firn liquid conductivity and major ion concentrations, as well as methane concentrations in the ice. The closed and open porosity volumes of firn samples were obtained by the two independent methods of pycnometry and tomography, that yield similar results. The measured increase of the closed porosity with density is used to estimate the air content trapped in the ice with the aid of a simple gas trapping model. Results show a discrepancy, with the model trapping too much air. Experimental errors have been considered but do not explain the discrepancy between the model and the observations. The model and data can be reconciled with the introduction of a reduced compression of the closed porosity compared to the open porosity. Yet, it is not clear if this limited compression of closed pores is the actual mechanism responsible for the low amount of air in the ice. High resolution density measurements reveal the presence of a strong layering, manifesting itself as centimeter scale variations. Despite this heterogeneous stratification, all layers, including the ones that are especially dense or less dense compared to their surroundings, display similar pore morphology and closed porosity as function of density. This implies that all layers close in a similar way, even though some close in advance or later compared to the bulk firn. Investigation of the chemistry data suggests that in the trapping zone, the observed stratification is partly related to the presence of chemical impurities.

Description: The effective size of snow grains (reff) affects the reflectivity of snow surfaces and thus the local surface energy budget in particular in polar regions. Therefore, the specific surface area (SSA) was monitored for a two-month period in central Antarctica (Kohnen research station) during austral summer 2013/14. The data were retrieved on the basis of spectral surface albedo measurements collected by the COmpact RAdiation measurement System (CORAS, ground-based) and the Spectral Modular Airborne Radiation measurement sysTem (SMART, airborne). The Snow Grain Size and Pollution amount (SGSP) algorithm, originally developed to analyze spaceborne reflectance measurements by the MODerate Resolution Imaging Spectroradiometer (MODIS), was modified and applied to the ground-based and airborne observations collected in this study. Furthermore, spectral ratios of surface albedo at 1280 nm and 1100 nm wavelength were used to reduce the retrieval uncertainty. Additionally, the algorithm originally developed for cloudless conditions was adapted to handle overcast conditions. Optical in situ observations of SSA utilizing an IceCube device were used to validate the retrieval results. The SSA retrieved from CORAS observations varied between 27 m2 kg-1 and 86 m2 kg-1. Snowfall events caused distinct SSA maxima which were often followed by a gradual decrease in SSA due to snow metamorphism and wind-induced transport of fresh fallen ice crystals (vice versa for reff). SSA retrieved by data from CORAS and MODIS agree with the in situ observations within the ranges given by the measurement uncertainties. However, SSA retrieved by the airborne SMART observations underestimated the ground-based observations by a factor of 2.1 (overestimation of reff).

Description: In order to interpret the paleoclimatic record stored in the air enclosed in polar ice cores, it is crucial to understand the fundamental lock-in process. Within the porous firn, bubbles are sealed continuously until the respective horizontal layer reaches a critical porosity. Present-day firn models use a postulated temperature dependence of this value as the only parameter to adjust to the surrounding conditions of individual sites. However, no direct measurements of the firn microstructure could confirm these assumptions. Here we show that the critical porosity is a universal constant by providing a statistically solid data set of μm-resolution 3D X-ray computer tomographic measurements for ice cores representing different extremes of the temperature and accumulation ranges. We demonstrate why indirect measurements yield misleading data and substantiate our observations by applying percolation theory as a theoretical framework for bubble trapping. Incorporation of our results does significantly influence the dating of trace gas records, changing gas age–ice age differences by up to more than 1000 years. This will help resolve inconsistencies, such as differences between East Antarctic δ15N records (as a proxy for firn height) and model results. We expect our findings to be the basis for improved firn air and densification models, leading to lower dating uncertainties. The reduced coupling of proxies and surrounding conditions may allow for more sophisticated reinterpretations of trace gas records in terms of paleoclimatic changes and will foster the development of new proxies, such as the air content as a marker of local insolation.

Description: Along a traverse through North Greenland in May 2015 we collected snow cores up to 2 m depth and analyzed their density and water isotopic composition. A new sampling technique and an adapted algorithm for comparing data sets from different sites and aligning stratigraphic features are presented. We find good agreement of the density layering in the snowpack over hundreds of kilometers, which allows the construction of a representative density profile. The results are supported by an empirical statistical density model, which is used to generate sets of random profiles and validate the applied methods. Furthermore we are able to calculate annual accumulation rates, align melt layers and observe isotopic temperatures in the area back to 2010. Distinct relations of δ18O with both accumulation rate and density are deduced. Inter alia the depths of the 2012 melt layers and high-resolution densities are provided for applications in remote sensing.

Description: Quantifying the magnitude of post-depositional processes affecting the isotopic composition of surface snow is essential for a more accurate interpretation of ice core data. To achieve this, high temporal resolution measurements of both lower atmospheric water vapor and surface snow isotopic composition are required. This study presents continuous measurements of water vapor isotopes performed in East Antarctica (Kohnen station) from December 2013 to January 2014 using a laser spectrometer. Observations have been compared with the outputs of two atmospheric general circulation models (AGCMs) equipped with water vapor isotopes: ECHAM5-wiso and LMDZ5Aiso. During our monitoring period, the signals in the 2 m air temperature T, humidity mixing ratio q and both water vapor isotopes δD and δ18O are dominated by the presence of diurnal cycles. Both AGCMs simulate similar diurnal cycles with a mean amplitude 30 to 70 % lower than observed, possibly due to an incorrect simulation of the surface energy balance and the boundary layer dynamics. In parallel, snow surface samples were collected each hour over 35 h, with a sampling depth of 2–5 mm. A diurnal cycle in the isotopic composition of the snow surface is observed in phase with the water vapor, reaching a peak-to-peak amplitude of 3 ‰ for δD over 24 h (compared to 36 ‰ for δD in the water vapor). A simple box model treated as a closed system has been developed to study the exchange of water molecules between an air and a snow reservoir. In the vapor, the box model simulations show too much isotopic depletion compared to the observations. Mixing with other sources (advection, free troposphere) has to be included in order to fit the observations. At the snow surface, the simulated isotopic values are close to the observations with a snow reservoir of  ∼ 5 mm depth (range of the snow sample depth). Our analysis suggests that fractionation occurs during sublimation and that vapor–snow exchanges can no longer be considered insignificant for the isotopic composition of near-surface snow in polar regions.

Description: Advances in trace gas analysis allow localised, non-atmospheric features to be resolved in ice cores, superimposed on the coherent atmospheric signal. These high-frequency signals could not have survived the low-pass filter effect that gas diffusion in the firn exerts on the atmospheric history and therefore do not result from changes in the atmospheric composition at the ice sheet surface. Using continuous methane (CH4) records obtained from five polar ice cores, we characterise these non-atmospheric signals and explore their origin. Isolated samples, enriched in CH4 in the Tunu13 (Greenland) record are linked to the presence of melt layers. Melting can enrich the methane concentration due to a solubility effect, but we find that an additional in situ process is required to generate the full magnitude of these anomalies. Furthermore, in all the ice cores studied there is evidence of reproducible, decimetre-scale CH4 variability. Through a series of tests, we demonstrate that this is an artifact of layered bubble trapping in a heterogeneous-density firn column; we use the term “trapping signal” for this phenomenon. The peak-to-peak amplitude of the trapping signal is typically 5 ppb, but may exceed 40 ppb. Signal magnitude increases with atmospheric CH4 growth rate and seasonal density contrast, and decreases with accumulation rate. Significant annual periodicity is present in the CH4 variability of two Greenland ice cores, suggesting that layered gas trapping at these sites is controlled by regular, seasonal variations in the physical properties of the firn. Future analytical campaigns should anticipate high-frequency artifacts at high-melt ice core sites or during time periods with high atmospheric CH4 growth rate in order to avoid misinterpretation of such features as past changes in atmospheric composition.

Description: In low-accumulation regions, the reliability of δ18O-derived temperature signals from ice cores within the Holocene is unclear, primarily due to the small climate changes relative to the intrinsic noise of the isotopic signal. In order to learn about the representativity of single ice cores and to optimise future ice-core-based climate reconstructions, we studied the stable-water isotope composition of firn at Kohnen Station, Dronning Maud Land, Antarctica. Analysing δ18O in two 50 m long snow trenches allowed us to create an unprecedented, two-dimensional image characterising the isotopic variations from the centimetre to the 100-metre scale. Our results show seasonal layering of the isotopic composition but also high horizontal isotopic variability caused by local stratigraphic noise. Based on the horizontal and vertical structure of the isotopic variations, we derive a statistical noise model which successfully explains the trench data. The model further allows one to determine an upper bound for the reliability of climate reconstructions conducted in our study region at seasonal to annual resolution, depending on the number and the spacing of the cores taken.

Description: Stable water isotopes in firn and ice cores are extensively used to infer past climate changes. In low-accumulation regions their interpretation is however challenged by poorly constrained effects that may influence the initial isotope signal during and after deposition. This is reflected in snow-pit isotope data from Kohnen Station, Antarctica, which exhibit a clear seasonal cycle but also strong inter-annual variations that contradict local temperature observations. These inconsistencies persist even after averaging many profiles and are thus not explained by local stratigraphic noise. Previous studies have suggested that post-depositional processes may significantly influence the isotopic composition of East Antarctic firn. Here, we reject the hypothesis of post-depositional change within the open-porous firn beyond diffusion and densification. To this end, we analyse 22 stable water isotope profiles obtained from two snow trenches at Kohnen Station and examine the temporal isotope modifications by comparing the new with published trench data extracted 2 years earlier. The initial isotope profiles undergo changes over time due to downward-advection, firn diffusion and densification in magnitudes consistent with independent estimates. Beyond that, we find no evidence for additional modification of the original isotope record. These results show that the discrepancy between local temperatures and isotopes most likely originates from spatially coherent processes prior to or during deposition, such as precipitation intermittency or systematic isotope modifications acting on drifting or loose surface snow.