100m-scale isotopic (δ18O) variability of the top-meter at location B52, East Antarctica

Small-scale (100 meter) isotopic composition of the top-meter of the snowpack around Kohnen station, Droning-Maud Land, East-Antarctica. The snow was sampled with the dual-tube sampling technique and the isotopic analysis were realized by CRDS (Cavity-Ring-Down Spectroscopy, l2130-i, Picarro Inc.) at the Alfred-Wegener-Institut Helmholtz-Zentrum für Polar-und Meeresforschung, in Bremerhaven, Germany

5km-scale isotopic (δ18O) variability of the top-meter between locations B50 and B49, East Antarctica

Intermediate-scale (5 kilometers) isotopic composition of the top-meter of the snowpack around Kohnen station, Dronning-Maud Land, East-Antarctica. The snow was sampled with the dual-tube sampling technique and the isotopic analysis were realized by CRDS (Cavity-Ring-Down Spectroscopy, l2130-i, Picarro Inc.) at the Alfred-Wegener-Institut Helmholtz-Zentrum für Polar-und Meeresforschung, in Bremerhaven, Germany

A dual-tube sampling technique for snowpack studies

The validity of any glaciological paleo proxy used to interpret climate records is based on the level of understanding of their transfer from the atmosphere into the ice sheet and their recording in the snowpack. Large spatial noise in snow properties is observed, as the wind constantly redistributes the deposited snow at the surface routed by the local topography. To increase the signal-tonoise ratio and getting a representative estimate of snow properties with respect to the high spatial variability, a large number of snow profiles is needed. However, the classical way of obtaining profiles via snow-pits is time and energy-consuming, and thus unfavourable for large surface sampling programs. In response, we present a dual-tube technique to sample the upper metre of the snowpack at a variable depth resolution with high efficiency. The developed device is robust and avoids contact with the samples by exhibiting two tubes attached alongside each other in order to (1) contain the snow core sample and (2) to access the bottom of the sample, respectively. We demonstrate the performance of the technique through two case studies in East Antarctica where we analysed the variability of water isotopes at a 100 m and 5 km spatial scales

Major elemental concentrations from NGRIP ice core across the interstadial period GI-21.2

Several abrupt shifts from periods of extreme cold (Greenland stadials, GS) to relatively warmer conditions (Greenland interstadials, GI) called Dansgaard-Oeschger events are recorded in the Greenland ice cores. Using cryo-cell UV-laser-ablation inductively-coupled-plasma mass spectrometry (UV-LA-ICPMS), we analysed a 2.85 m NGRIP ice core section (~ 250 years; 2691.50–2688.65 m depth) across the transitions of GI-21.2, a short-lived interstadial prior to interstadial GI-21.1 (GI-21.2: 84.87–85.09 ka b2k). GI-21.2 is a ~100-year-long period with d18O values 3–4 per mil higher than the following ~200 years of stadial conditions (GS-21.2), which precede the major GI-21.1 warming. We report concentrations of "major" elements indicative of dust and/or sea salt (Na, Fe, Al, Ca, Mg) at a spatial resolution of ~ 200 µm, while maintaining detection limits in the low-ppb range, thereby achieving sub-annual time resolution even in deep NGRIP ice. We present an improved external calibration and quantification procedure using a set of five ice standards made from aqueous (international) standard solutions. Our results show that element concentrations decrease drastically (more than tenfold) at the warming onset of GI-21.2 at the scale of a single year, followed by relatively low concentrations characterizing the interstadial part before gradually reaching again typical stadial values

Fe²⁺ in ice cores as a new potential proxy to detect past volcanic eruptions

Volcanic eruptions are widely used in ice core science to date or synchronize ice cores. Volcanoes emit large amounts of SO₂ that is subsequently converted inthe atmosphere into sulfuric acid/sulphate.Its discrete and continuous quantification is currently used to determine the ice layers impacted by volcanic emissions, but available high-resolution sulphate quantification methods in ice core (Continuous Flow Analysis (CFA)) struggle with insufficient sensitivity. Here, we present a new high-resolution CFA chemiluminescence method for the continuous determination of Fe²⁺ species in ice cores thatshowsclear Fe²⁺ peaks concurrent with volcanicsulphate peaks in the ice core record. The method, applied on a Greenland ice core, correctly identifies all volcanic eruptions from between 1588 to 1611 and from 1777 to 1850. The method has a detection limit of ∽5pgg⁻¹ and a quadratic polynomial calibration range of up to at least 1760 pg g⁻¹. Our results show that Fe²⁺ is a suitable proxy for identifying past volcanic events

Ice-nucleating particle concentrations of the past: insights from a 600-year-old Greenland ice core

Ice-nucleating particles (INPs) affect the microphysics in cloud and precipitation processes. Hence, they modulate the radiative properties of clouds. However, atmospheric INP concentrations of the past are basically unknown. Here, we present INP measurements from an ice core in Greenland, which dates back to the year 1370. In total 135 samples were analyzed with the FRIDGE droplet freezing assay in the temperature range from −14 to −35 ∘C. The sampling frequency was set to 1 in 10 years from 1370 to 1960. From 1960 to 1990 the frequency was increased to one sample per year. Additionally, a few special events were probed, including volcanic episodes. The typical time coverage of a sample was on the order of a few months. Historical atmospheric INP concentrations were estimated with a conversion factor, which depends on the snow accumulation rate of the ice core, particle dry deposition velocity, and wet scavenging ratio. Typical atmospheric INP concentrations were on the order of 0.1 L−1 at −25 ∘C. The INP variability was found to be about 1–2 orders of magnitude. Yet, the short-term variability from samples over a seasonal cycle was considerably lower. INP concentrations were significantly correlated to some chemical tracers derived from continuous-flow analysis (CFA) and ion chromatography (IC) over a broad range of nucleation temperatures. The highest correlation coefficients were found for the particle concentration (spherical diameter dp > 1.2 µm). The correlation is higher for a time period of seasonal samples, where INP concentrations follow a clear annual pattern, highlighting the importance of the annual dust input in Greenland from East Asian deserts during spring. Scanning electron microscopy (SEM) analysis of selected samples found mineral dust to be the dominant particle fraction, verifying their significance as INPs. Overall, the concentrations compare reasonably well to present-day INP concentrations, albeit they are on the lower side. However, we found that the INP concentration at medium supercooled temperatures differed before and after 1960. Average INP concentrations at −23, −24, −25, −26, and −28 ∘C were significantly higher (and more variable) in the modern-day period, which could indicate a potential anthropogenic impact, e.g., from land-use change