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Abstract Ice nucleating particles (INPs) affect the cloud radiative budget in the rapidly warming Arctic by changing the cloud liquid/ice phase balance. Dust emitted in the Arctic (Arctic dust) has been suggested to be a major contributor to INPs in the Arctic lower troposphere. However, how Arctic dust and its impacts on ice nucleation change with Arctic warming has not been explored. Here we find that the simulated dust emission flux in the Arctic (>60°N) in global model simulations increases by 20% from 1981–1990 to 2011–2020. This increase weakens the sensitivity of ice nucleation in Arctic lower tropospheric clouds to warming by 40% compared to the case without considering Arctic dust emission increases. Our results demonstrate a better understanding of the counterbalancing feedbacks of Arctic dust (i.e., increasing emissions and decreasing ice nucleation efficiency) is needed for more accurate estimates of changes in ice nucleation in the rapidly changing Arctic climate.

In recent decades, surface melting on the inland Greenland ice sheet has increased, leading to significant meltwater-refreezing in the snow and firn. Increased knowledge of the physical and chemical characteristics of these melt features (i.e., ice layers) is needed to help estimate future global sea-level rise. Here, using a combination of microscopy and spectroscopy, we investigate the size, shape, location, and chemical compositions of inclusions in 12 ice layers of the SIGMA-A ice core in the northwestern Greenland ice sheet (78°03′06″N, 67°37′42″W, 1490 m a.s.l.). In the ice layers, we found inclusions exceeding 30 μm diameter that could only be formed by melting–refreezing, which we classify into columnar-, particle-, and rod-like inclusions. We propose that the smaller columnar- and particle-like inclusions of solid Na2SO4⋅10H2O and CaSO4⋅2H2O form first, within the ice grains, followed by the larger rod-like inclusions of brines with mainly Na+ and Cl− in grain boundaries. Our results suggest a new proxy that may help identify past warm climates in deeper ice cores in Greenland and for studying future ice sheet melting behavior.

Summer sea ice retreat in the high latitude North Atlantic since 2000 is associated with increases in oceanic emissions of dimethyl sulfide, according to a record of methane sulfonic acid fluxes from an ice core in southeast Greenland.

Abstract Previous reconstructions of summer temperatures from ice cores have relied on a statistical relationship between a melt layer and temperature observed at nearby stations. This study presents a novel method for reconstructing summer temperatures from melt layers in ice cores using an energy balance model that incorporates heat conduction and meltwater refreezing in the firn. We use the seasonal patterns in the ERA‐Interim reanalysis data set for an ice core site to calculate the amounts of refreezing water within the firn under various summer mean temperature (SMT) and annual precipitation conditions, and prepared calibration tables containing these three variables. We then estimate the SMTs from the refreezing amount and annual accumulation, both of which can be obtained from an ice core. We apply this method to four ice cores that were recovered from sites with different climates: two sites on the Greenland Ice Sheet, one in Alaska, and one in Russian Altai. The reconstructed SMTs show comparable variations with those of observed temperatures at nearby stations. The nonlinear relationship between SMT and melt layer thickness differs between sites, indicating that a single linear approximation cannot be employed to estimate SMT. Sensitivity analyses suggest that the annual temperature range, amount of annual precipitation, and firn albedo (which is a time‐invariant value in the model) significantly affect the relationship between SMT and melt layer thickness. This new method provides an alternative to existing approaches and yields an independent estimate of SMT from ice cores that have been affected by melting.

From glaciological observations, we found spatial variation in the input of insoluble particles (ISP) on a glacier surface from atmospheric deposition and outcropping at the surface of the glacier by surface ablation at the ablation area of the Qaanaaq Ice Cap in northwestern Greenland. Possible sources of ISP input to the glacier surface were outcropping at the surface of the glacier by ablation at intermediate and low elevations, and from atmospheric deposition at high elevations. The annual atmospheric deposition of ISP was larger at high elevations than at intermediate and low elevations. The annual abundance of outcropping ISP was larger at intermediate elevations than at low elevations, where the annual ablation rate of the glacier surface was 1.5 times larger than at intermediate elevations. The ISP concentration in the glacier ice at intermediate sites was approximately 10 times larger than at low sites. The water stable isotopes of glacier ice at intermediate sites indicated that glacier ice at the intermediate sites did not form since the last glacial maximum, possibly the Holocene Thermal Maximum. Therefore, the accumulation of the ISP, which is outcropping at the intermediate site, occurred at high elevations after Holocene Thermal Maximum.

Deep ice coring to bedrock (3028m in depth) at Dome Fuji Station is planned during three successive summer seasons starting from 2003/2004. An improved JARE deep ice core drill (12.2m in length and 3.8m in maximum core length) was developed in December 2001 for the ice coring at Dome Fuji. In January/February of 2002,we performed experiments on drill performance using artificial ice blocks in Rikubetsu, Hokkaido. In this paper, we outline the experiment and report the results. It was found through the experiment that an ice core of 3.8m length was smoothly obtained by the improved drill with three screws in the chip chamber and cutting pitch of 5mm/cycle. About 45000 small holes 1.2mm in diameter were made on the surface of the chip chamber. These small holes enabled liquid to circulate between cutters and outside of the drill through the chip chamber in the drill. The dry density of the chips was 440 to 500kg/m^3 and the chip recovery rate during ice coring was 65 to 91%. A check valve installed at the bottom of the chip chamber to prevent outflow of chips from the drill was not tested enough, but more durability is needed for the valve. The newly developed motor system and core catchers of the drill worked perfectly. The average coring speed was 24.5cm/min with cutting pitch of 5mm/cycle. The average power consumption during ice coring was 171W.

We developed a Handheld Integrating Sphere Snow Grain Sizer (HISSGraS) for field use to measure the specific surface area (SSA) of snow. In addition to snow samples, HISSGraS can directly measure snow surfaces and snow pit walls. The basic measurement principle is the same as that of the IceCube SSA instrument. The retrieval algorithm for SSA from reflectance employs two conversion equations formulated using spherical and nonspherical grain shape models. We observed SSAs using HISSGraS, IceCube and the gas adsorption method in a snowfield in Hokkaido, Japan. Intercomparison of the results confirmed that with HISSGraS direct measurement, SSA profile observations can be completed in just ~1/10 the time required for measurement of snow samples. Our results also suggest that HISSGraS and IceCube have similar accuracy when the same snow samples are measured using the same grain shape model. However, SSAs of near-surface snow layers measured using the three techniques exhibited some biases, possibly due to rapid snow metamorphism or melting during measurement and some technical issues with optical techniques. When excluding SSA data for the surface layer, which metamorphosed remarkably during measurement, IceCube- and HISSGraS-derived SSAs correlated strongly with those obtained by gas adsorption and HISSGraS accuracy is 21–34%.

The roles and impacts of black carbon (BC), an important aerosol species affecting Earth's radiation budget, are not well understood owing to lack of accurate long-term observations. To study the temporal changes in BC since the pre-industrial period, we analysed BC in an ice core drilled in northwest Greenland. Using an improved technique for BC measurement and a continuous flow analysis system, we obtained accurate and high temporal resolution records of BC particle size and mass/number concentrations for the past 350 years. Number and mass concentrations, which both started to increase in the 1870s associated with inflow of anthropogenically derived BC, reached their maxima in the 1910s-1920s and then subsequently decreased. On the basis of backward trajectory analyses, we found that North America was the dominant source region of the anthropogenic BC in the ice core. The increase in anthropogenic BC shifted the annual concentration peaks of BC from summer to winter-early spring. After BC concentrations diminished to pre-industrial levels, the annual peak concentration of BC returned to the summer. We found that anthropogenic BC particles were larger than biomass burning BC particles. By separating the BC in winter and summer, we reconstructed the temporal variations in BC that originated from biomass burning, including the period with large anthropogenic input. The BC that originated from biomass burning showed no trend of increase until the early 2000s. Finally, possible albedo reductions due to BC are discussed. Our new data provide key information for validating aerosol and climate models, thereby supporting improved projections 31 of future climate and environment. [ABSTRACT FROM AUTHOR]

Ice cores can provide long-term records of black carbon (BC), an important aerosol species closely linked to the climate and environment. However, previous studies of ice cores only analysed BC particles with diameter of <600-850 nm, which could have led to underestimation of BC mass concentrations. Information on the size distribution of BC particles is very limited, and there are no Arctic ice core records of the temporal variation in BC size distribution. In this study, we applied a recently developed improved technique to analyse the BC concentration in an ice core drilled at the SIGMA-D site in northwest Greenland. The improved technique, which uses a modified Single-Particle Soot Photometer and a high-efficiency nebulizer, widens the measurable range of BC particle size. For high-resolution continuous analyses of ice cores, we developed a continuous flow analysis (CFA) system (resolution: 10-40 mm). Coupling of the improved BC measurement technique with the CFA system allows accurate high-resolution measurements of the size distribution and concentration of BC particles with diameter between 70 nm and 4 µm, with minimal particle losses. Using this technique, we reconstructed the size distributions and the number and mass concentrations of BC particles during the past 350 years. On the basis of the size distributions, we assessed the underestimation of BC mass concentrations measured using the conventional method. For the period 2003-2013, the underestimation of the average mass concentration would have been 12%-17% for the SIGMA-D core. [ABSTRACT FROM AUTHOR]

Alpine ice core research has long focused on a few suitable drilling sites at high elevation in the Western European Alps, assuming that the counterparts at lower elevation in the eastern sector are unsuitable for paleoenvironmental studies, due to the presence of melting and temperate basal conditions. However, it has been demonstrated that even in the Eastern Alpine range, below 4,000 m a.s.l., cold ice frozen to bedrock can exist. In fact, millennial-old ice has been found at some locations, such as at the Weißseespitze (WSS) summit ice cap (Ӧtztal Alps, 3,499m a.s.l.), where about 6 kyrs appear locked into 10mof ice. In this work, we present a full profile of the stable water isotopes (δ18O, δ²H), major ions (Na+, K+, Mg2+, Ca2+, NH4+, Cl-, NO3-, SO42-), levoglucosan, and microcharcoal for two parallel ice cores drilled at the Weißseespitze cap. We find that, despite the ongoing ice loss, the chemical and isotopic signatures appear preserved, and may potentially offer an untapped climatic record. This is especially noteworthy considering that chemical signals of other archives at similar locations have been partially or full corrupted by meltwater (i.e., Silvretta glacier, Grand Combin glacier, Ortles glacier). In addition, the impurity concentration near the surface shows no signs of anthropogenic contamination at WSS, which constrains the age at the surface to fall within the pre-industrial age. [ABSTRACT FROM AUTHOR]

In situ meteorological data are essential to better understand ongoing environmental changes in the Arctic. Here, we present a dataset of quality-controlled meteorological observations by two automatic weather stations in northwest Greenland from July 2012 to the end of August 2020. The stations were installed in an accumulation area on the Greenland Ice Sheet (SIGMA-A site, 1490 m a.s.l.) and near the equilibrium line of the Qaanaaq Ice Cap (SIGMA-B site, 944 m a.s.l.). We describe the two-step sequence of quality-control procedures that we used to create increasingly reliable datasets by masking erroneous data records. We analyzed the resulting 2012-2020 time series of air temperature, positive degree-days, snow height, surface albedo, and histograms of longwave radiation (a proxy of cloud formation frequency). We found that snow height increased and albedo remained steady at the SIGMA-A site, whereas high air temperatures and clear-sky conditions prevailed while snow height and albedo decreased in the summers of 2015, 2019, and 2020 at the SIGMA-B site. Therefore, it appears that these weather conditions led to notable snow height degradation at the SIGMA-B site but not at the SIGMA-A site. We anticipate that this quality-control method and these datasets will aid in climate studies of northwest Greenland as well as contribute to the advancement of broader polar climate studies. [ABSTRACT FROM AUTHOR]

In order to construct reliable deposited-aerosol database on the Anthropocene (from 1850 to 2020), we obtained a 250-meter-long ice core from the Southeastern Greenland Dome on May and June 2021, where is one of the highest accumulation domes in Greenland. The age of the ice core at a depth of 250 m was roughly estimated to be AD 1827 based on the timescale from a previously analyzed shallower ice core. The age of the sampled ice core satisfied the prerequisite conditions for constructing aerosol deposition database for Anthropocene. In addition, surface elevation, borehole temperatures, and internal stratigraphy of the ice sheet were performed, and meteorological and snow-pit observations were also conducted. Furthermore, we sampled aerosol and snow from the ice sheet for chemical and physical analyses. [ABSTRACT FROM AUTHOR]

Previous studies reconstructing summer temperature from an ice core relied on statistical relationship between melt feature and instrumental temperature observed at a nearby station. This study demonstrates a novel method to reconstruct summer temperature from ice layer thickness in an ice core using an energy balance model, in which heat conduction and refreezing of meltwater in firn are taken into account. Using seasonal patterns of the ERA-Interim reanalysis dataset for an ice core site, we calculated amounts of refreezing water within firn under various settings of summer mean temperature (SMT) and annual precipitation, and prepared lookup tables containing these three variables. We then estimated SMT from the refreezing amount and annual accumulation, both available in an ice core. We applied this method to four ice cores drilled in the sites of different climates; two sites on the Greenland Ice Sheet, one in Alaska, and one in Russian Altai Mountains. Reconstructed SMTs show comparable variations to the temperatures observed at nearby stations. Relationships between SMT and ice layer thickness differ site by site, indicating that a single approximation cannot be applicable to estimate SMT. Sensitivity analyses suggest that annual temperature range, amount of annual precipitation and firn albedo setting significantly affect the relationship between SMT and ice layer thickness. This new method provides alternative and independent estimation of SMT from ice cores affected by melting. [ABSTRACT FROM AUTHOR]

Sea salts and halogens in aerosols, frost flowers, and brine play an important role in atmospheric chemistry in polar regions. Simultaneous sampling and observations of frost flowers, brine, and aerosol particles were conducted around Siorapaluk in northwestern Greenland during December 2013 to March 2014. Results show that water-soluble frost flower and brine components are sea-salt components (e.g., Na+, Cl−, Mg2+, K+, Ca2+, Br−, and iodine). Concentration factors of sea-salt components of frost flowers and brine relative to seawater were 1.14–3.67. Sea-salt enrichment of Mg2+, K+, Ca2+, and halogens (Cl−, Br−, and iodine) in frost flowers is associated with sea-salt fractionation by precipitation of mirabilite and hydrohalite. High aerosol number concentrations correspond to the occurrence of higher abundance of sea-salt particles in both coarse and fine modes, and blowing snow and strong winds. Aerosol number concentrations, particularly in coarse mode, are increased considerably by release from the sea-ice surface under strong wind conditions. Sulfate depletion by sea-salt fractionation was found to be limited in sea-salt aerosols because of the presence of non-sea-salt (NSS) SO42−. However, coarse and fine sea-salt particles were found to be rich in Mg. Strong Mg enrichment might be more likely to proceed in fine sea-salt particles. Magnesium-rich sea-salt particles might be released from the surface of snow and slush layer (brine) on sea ice and frost flowers. Mirabilite-like and ikaite-like particles were identified only in aerosol samples collected near new sea-ice areas. From the field evidence and results from earlier studies, we propose and describe sea-salt cycles in seasonal sea-ice areas. [ABSTRACT FROM AUTHOR]

Sea-salts and halogens in aerosols, frost flowers and brine play an important role in atmospheric chemistry in polar regions. Simultaneous sampling and observations of frost flowers, brine, and aerosol particles were conducted around Siorapaluk in north-western Greenland during December 2013-March 2014. Results show that water-soluble frost flower and brine constituents were sea salts (e.g., Na+, Cl-, Mg2+, and Br-). Concentration factors of sea-salt constituents of frost flowers and brine relative to seawater were 1.14-3.67. Sea-salt enrichments of Mg2+, K+, Ca2+, and halogens (Cl-, Br-, and I) in frost flowers were associated with sea-salt fractionation by precipitation of mirabilite and hydrohalite. Aerosol number concentrations, particularly in coarse mode, were increased considerably by release from the sea-ice surface under strong wind conditions. Sulphate depletion by sea-salt fractionation was found to be slight in sea-salt aerosols because of heterogeneous SO42- formation on sea-salt particles. However, coarse and fine sea-salt particles were found to be rich in Mg. Strong Mg enrichment might be more likely to proceed in fine sea-salt particles. Mg-rich sea-salt particles might be released from the sea-ice surface and frost flowers. Mirabilite-like and ikaite-like particles were identified only in aerosol samples collected near new sea-ice areas. [ABSTRACT FROM AUTHOR]

The Institute of Low Temperature Science at Hokkaido University conducted ice-core drilling in alpine glaciers in the northern North Pacific region to reconstruct climate change in this region for the past few hundred years. We drilled two ice cores in the Kamchatka Peninsula, Russia. An ice core with a length of 211 m was drilled on a glacier at the summit caldera of Ushkovsky mountain in 1998. A second core, with a length of 115 m (until bedrock was reached), was drilled on a glacier at the summit caldera of Ichinsky mountain in 2006. We drilled three further ice cores in Alaska, USA. Two ice cores with lengths of 50 and 212 m were drilled on a glacier at the summit caldera of Mount Wrangell in 2003 and 2004. The third ice core was drilled on the ice divide among three glaciers, Black Rapids, Trident and Susitna glaciers, which represent a flat saddle north of Aurora Peak in the Alaska Range. This paper details the field operations and characteristics of the different ice-drilling systems used and the problems encountered. [ABSTRACT FROM AUTHOR]

To study the glaciological processes controlling the mass budget of Greenland's peripheral glaciers and ice caps, field measurements were carried out on Qaanaaq ice cap, a 20 km long ice cap in northwestern Greenland. In the summer of 2012, we measured surface melt rate, ice flow velocity and ice thickness along a survey route spanning the ice margin (200ma.s.l.) to the ice-cap summit (1110ma.s.l.). Melt rates in the ablation area were clearly influenced by dark materials covering the ice surface, where degree-day factors varied from 5.44mmw.e. K-1 d-1 on a clean surface to 8.26mmw.e. K-1 d-1 in the dark regions. Ice velocity showed diurnal variations, indicating the presence of surface-meltwater induced basal sliding. Mean ice thickness along the survey route was 120 m, with a maximum thickness of 165 m. Ice velocity and temperature fields were computed using a thermomechanically coupled numerical glacier model. Modelled ice temperature, obtained by imposing estimated annual mean air temperature as the surface boundary condition, was substantially lower than implied by the observed ice velocity. This result suggests that the ice dynamics and thermodynamics of the ice cap are significantly influenced by heat transfer from meltwater and changing ice geometry. [ABSTRACT FROM AUTHOR]