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Abstract On polar ice sheets, water vapor interacts with surface snow, and through the exchange of water molecules, imprints an isotopic climate signal into the ice sheet. This exchange is not well understood due to sparse observations in the atmosphere. There are currently no published vertical profiles of water isotopes above ice sheets that span the planetary boundary layer and portions of the free troposphere. Here, we present a novel data set of water‐vapor isotopes (O, D, ) and meteorological variables taken by fixed‐wing uncrewed aircraft on the northeast Greenland Ice Sheet (GIS). During June–July (2022), we collected 104 profiles of water‐vapor isotopes and meteorological variables up to 1,500 m above ground level. Concurrently, surface snow samples were collected at 12‐hr intervals, allowing connection to surface‐snow processes. We pair observations with modeling output from a regional climate model as well as an atmospheric transport and water‐isotope distillation model. Climate model output of mean temperature and specific humidity agrees well with observations, with a mean difference of +0.095°C and −0.043 g/kg (−2.91%), respectively. We find evidence that along an air parcel pathway, the distillation model is not removing enough water prior to onsite arrival. Below the mean temperature inversion (200 m), water‐isotope observations indicate a kinetic fractionating process, likely the result of mixing sublimated vapor from the ice sheet surface along with an unknown fraction of katabatic wind vapor. Modeled does not agree well with observations, a result that requires substantial future analysis of kinetic fractionation processes along the entire moisture pathway. 

Climate change is a major concern to undergraduate students. Understanding climate change relies on an understanding of polar regions. However, courses on polar regions are rare at undergraduate institutions. Polar ENgagement through GUided INquiry (PENGUIN) modules were designed to give students experience with polar research in a variety of standard courses, including physics, computer science, physical chemistry, and economics, through using course-specific and computational tools to analyze polar data. Here, we present a new PENGUIN module taught in a statistics class, in which students apply statistical tools to ice core data to reconstruct past temperature records. Quantitative student responses on pre- and post-surveys were collected in a quasi-experimental context to assess student knowledge gains for a test group of 91 students and a control group of 73 students (who did not complete the module). Test-group students made statistically significant increases of 25 to 46% on all six statistics questions, with a normalized gain of 56%. By contrast, control group statistics knowledge gains ranged from −4 to 25%, with statistically significant increases for only three questions and a normalized gain of 22%. For polar research questions, the test group demonstrated increases in correct responses to polar research questions (11 to 31%), with statistically significant improvements (p < .05) of 22-31% on 3 of 6 polar research questions. These findings support the conclusion that PENGUIN modules can successfully teach course concepts while increasing polar literacy. 

Abstract. We document the isotopic evolution of near-surface snow at the East Greenland Ice Core Project (EastGRIP) ice core site in northeast Greenland using a time-resolved array of 1 m deep isotope (δ18O, δD) profiles. The snow profiles were taken from May–August during the 2017–2019 summer seasons. An age–depth model was developed and applied to each profile, mitigating the impacts of stratigraphic noise on isotope signals. Significant changes in deuterium excess (d) are observed in surface snow and near-surface snow as the snow ages. Decreases in d of up to 5 ‰ occur during summer seasons after deposition during two of the three summer seasons observed. The d always experiences a 3 ‰–5 ‰ increase after aging 1 year in the snow due to a broadening of the autumn d maximum. Models of idealized scenarios coupled with prior work indicate that the summertime post-depositional changes in d (Δd) can be explained by a combination of surface sublimation, forced ventilation of the near-surface snow down to 20–30 cm, and isotope-gradient-driven diffusion throughout the column. The interannual Δd is also partly explained with isotope-gradient-driven diffusion, but other mechanisms are at work that leave a bias in the d record. Thus, d does not just carry information about source-region conditions and transport history as is commonly assumed, but also integrates local conditions into summer snow layers as the snow ages through metamorphic processes. Finally, we observe a dramatic increase in the seasonal isotope-to-temperature sensitivity, which can be explained solely by isotope-gradient-driven diffusion. Our results are dependent on the site characteristics (e.g., wind, temperature, accumulation rate, snow properties) but indicate that more process-based research is necessary to understand water isotopes as climate proxies. Recommendations for monitoring and physical modeling are given, with special attention to the d parameter. 

Abstract. Accurate boundary layer temperature and humidity profiles are crucial for successful forecasting of fog, and accurate retrievals of liquid water path are important for understanding the climatological significance of fog. Passive ground-based remote sensing systems such as microwave radiometers (MWRs) and infrared spectrometers like the Atmospheric Emitted Radiance Interferometer (AERI), which measures spectrally resolved infrared radiation (3.3 to 19.2 µm), can retrieve both thermodynamic profiles and liquid water path. Both instruments are capable of long-term unattended operation and have the potential to support operational forecasting. Here we compare physical retrievals of boundary layer thermodynamic profiles and liquid water path during 12 cases of thin (LWP<40 g m−2) supercooled radiation fog from an MWR and an AERI collocated in central Greenland. We compare both sets of retrievals to in-situ measurements from radiosondes and surface-based temperature and humidity sensors. The retrievals based on AERI observations accurately capture shallow surface-based temperature inversions (0–10 m a.g.l.) with lapse rates of up to −1.2 ∘C m−1, whereas the strength of the surface-based temperature inversions retrieved from MWR observations alone are uncorrelated with in-situ measurements, highlighting the importance of constraining MWR thermodynamic profile retrievals with accurate surface meteorological data. The retrievals based on AERI observations detect fog onset (defined by a threshold in liquid water path) earlier than those based on MWR observations by 25 to 185 min. We propose that, due to the high sensitivity of the AERI instrument to near-surface temperature and small changes in liquid water path, the AERI (or an equivalent infrared spectrometer) could be a useful instrument for improving fog monitoring and nowcasting, particularly for cases of thin radiation fog under otherwise clear skies, which can have important radiative impacts at the surface. 

Abstract. This study presents the first full annual cycle (2019–2020) of ambient surface aerosol particle number concentration measurements (condensationnuclei > 20 nm, N20) collected at Summit Station (Summit), in the centre of the Greenland Ice Sheet (72.58∘ N, −38.45∘ E; 3250 ma.s.l.). The mean surface concentration in 2019 was 129 cm−3, with the 6 h mean ranging between 1 and 1441 cm−3. The highest monthly mean concentrations occurred during the late spring and summer, with the minimum concentrations occurring in February (mean: 18 cm−3). High-N20 events are linked to anomalous anticyclonic circulation over Greenland and the descent of free-tropospheric aerosol down to the surface, whereas low-N20 events are linked to anomalous cyclonic circulation over south-east Greenland that drives upslope flow and enhances precipitation en route to Summit. Fog strongly affects particle number concentrations, on average reducing N20 by 20 % during the first 3 h of fog formation. Extremely-low-N20 events (< 10 cm−3) occur in all seasons, and we suggest that fog, and potentially cloud formation, can be limited by low aerosol particle concentrations over central Greenland.