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The availability of snow accumulation data is a critical factor in accurate Surface Mass Balance predictions of the Greenland Ice Sheet, which forms the base for predictions of sea level rise in a warming climate. Currently, this data remains deficient due to incomplete geographical coverage and poor temporal resolution. The Lightweight In Situ Analysis (LISA) box is a portable system built for fast and straightforward accumulation measurements on firn cores directly in the field. The sample cores are melted from one end, and Continuous Flow Analysis (CFA) of seasonally varying chemical impurities and conductivity in the melt water reveals annual layers in the firn. With additional firn density measurements with a typical depth resolution of 0.5−1m, the accumulation rate of the years that are represented in the core can be reconstructed to annual resolution. This thesis works towards a high-resolution density measurement method for the LISA box to achieve sub-annual accumulation rate resolution. An ultrasonic distance sensor now automates the melt speed measurement with high resolution. Furthermore, a liquid flow meter continuously measures the flow rate of melt water produced, which is proportional to the density of the melted sample section. The flow meter has an absolute accuracy of 10% for a flow rate of 100mL/min. Theoretically, a firn density measurement with an uncertainty of 15 − 17% could be achieved, with the low uncertainty for cores that are low density, have a large radius, and maintain a regular shape. The uncertainty could be further reduced by choosing a flow meter with higher accuracy. In practice however, to prevent water loss by overflow, the water is drained at a generously set rate. This induces air bubbles to the melt water that alter the flow rate measurements. Detailed sensitivity tests have shown that the effect can be corrected with a linear

Mercury is a pollutant of global concern, especially in the Arctic, where high levels are found in biota despite its remote location. Mercury is transported to the Arctic via atmospheric, oceanic and riverine long-range pathways, where it accumulates in aquatic and terrestrial ecosystems. While present-day mercury deposition in the Arctic from natural and anthropogenic emissions is extensively studied, the control of past climate changes on natural mercury variability remains unknown. Here we present an Arctic mercury record covering the Last Glacial Termination to the early Holocene epoch (15.7–9.0 thousand years before 2000 ce), collected as part of the East Greenland Ice-Core Project. We find a threefold increase in mercury depositional fluxes from the Last Glacial Termination into the early Holocene, which coincided with abrupt regional climate warming. Atmospheric chemistry modelling, combined with available sea-ice proxies, indicates that oceanic mercury evaporation and atmospheric bromine drove the increase in mercury flux during this climatic transition. Our results suggest that environmental changes associated with climate warming may contribute to increasing mercury levels in Arctic ecosystems.

Iodine has a significant impact on promoting the formation of new ultrafine aerosol particles and accelerating tropospheric ozone loss, thereby affecting radiative forcing and climate. Therefore, understanding the long-term natural evolution of iodine, and its coupling with climate variability, is key to adequately assess its effect on climate on centennial to millennial timescales. Here, using two Greenland ice cores (NEEM and RECAP), we report the Arctic iodine variability during the last 127,000 years. We find the highest and lowest iodine levels recorded during interglacial and glacial periods, respectively, modulated by ocean bioproductivity and sea ice dynamics. Our sub-decadal resolution measurements reveal that high frequency iodine emission variability occurred in pace with Dansgaard/Oeschger events, highlighting the rapid Arctic ocean-ice-atmosphere iodine exchange response to abrupt climate changes. Finally, we discuss if iodine levels during past warmer-than-present climate phases can serve as analogues of future scenarios under an expected ice-free Arctic Ocean. We argue that the combination of natural biogenic ocean iodine release (boosted by ongoing Arctic warming and sea ice retreat) and anthropogenic ozone-induced iodine emissions may lead to a near future scenario with the highest iodine levels of the last 127,000 years.

Large volcanic eruptions occurring in the last glacial period can be detected by their accompanying sulfuric acid deposition in continuous ice cores. Here we employ continuous sulfate and sulfur records from three Greenland and three Antarctic ice cores to estimate the emission strength, the frequency and the climatic forcing of large volcanic eruptions that occurred during the second half of the last glacial period and the early Holocene, 60–9 kyr before 2000 CE (b2k). Over most of the investigated interval the ice cores are synchronized, making it possible to distinguish large eruptions with a global sulfate distribution from eruptions detectable in one hemisphere only. Due to limited data resolution and large variability in the sulfate background signal, particularly in the Greenland glacial climate, we only list Greenland sulfate depositions larger than 20 kg km−2 and Antarctic sulfate depositions larger than 10 kg km−2. With those restrictions, we identify 1113 volcanic eruptions in Greenland and 737 eruptions in Antarctica within the 51 kyr period – for which the sulfate deposition of 85 eruptions is found at both poles (bipolar eruptions). Based on the ratio of Greenland and Antarctic sulfate deposition, we estimate the latitudinal band of the bipolar eruptions and assess their approximate climatic forcing based on established methods. A total of 25 of the identified bipolar eruptions are larger than any volcanic eruption occurring in the last 2500 years, and 69 eruptions are estimated to have larger sulfur emission strengths than the Tambora, Indonesia, eruption (1815 CE). Throughout the investigated period, the frequency of volcanic eruptions is rather constant and comparable to that of recent times. During the deglacial period (16–9 ka b2k), however, there is a notable increase in the frequency of volcanic events recorded in Greenland and an obvious increase in the fraction of very large eruptions. For Antarctica, the deglacial period cannot be distinguish

We present a record of melt events obtained from the East Greenland Ice Core Project (EastGRIP) ice core in central northeastern Greenland, covering the largest part of the Holocene. The data were acquired visually using an optical dark-field line scanner. We detect and describe melt layers and lenses, seen as bubble-free layers and lenses, throughout the ice above the bubble–clathrate transition. This transition is located at 1150 m depth in the EastGRIP ice core, corresponding to an age of 9720 years b2k. We define the brittle zone in the EastGRIP ice core as that from 650 to 950 m depth, where we count on average more than three core breaks per meter. We analyze melt layer thicknesses, correct for ice thinning, and account for missing layers due to core breaks. Our record of melt events shows a large, distinct peak around 1014 years b2k (986 CE) and a broad peak around 7000 years b2k, corresponding to the Holocene Climatic Optimum. In total, we can identify approximately 831 mm of melt (corrected for thinning) over the past 10 000 years. We find that the melt event from 986 CE is most likely a large rain event similar to that from 2012 CE, and that these two events are unprecedented throughout the Holocene. We also compare the most recent 2500 years to a tree ring composite and find an overlap between melt events and tree ring anomalies indicating warm summers. Considering the ice dynamics of the EastGRIP site resulting from the flow of the Northeast Greenland Ice Stream (NEGIS), we find that summer temperatures must have been at least 3 ± 0.6 ∘C warmer during the Early Holocene compared to today.

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.

Sea ice decline in the North Atlantic and Nordic Seas has been proposed to contribute to the repeated abrupt atmospheric warmings recorded in Greenland ice cores during the last glacial period, known as Dansgaard-Oeschger (D-O) events. However, the understanding of how sea ice changes were coupled with abrupt climate changes during D-O events has remained incomplete due to a lack of suitable high-resolution sea ice proxy records from northwestern North Atlantic regions. Here, we present a subdecadal-scale bromine enrichment (Brenr) record from the NEEM ice core (Northwest Greenland) and sediment core biomarker records to reconstruct the variability of seasonal sea ice in the Baffin Bay and Labrador Sea over a suite of D-O events between 34 and 42 ka. Our results reveal repeated shifts between stable, multiyear sea ice (MYSI) conditions during cold stadials and unstable, seasonal sea ice conditions during warmer interstadials. The shift from stadial to interstadial sea ice conditions occurred rapidly and synchronously with the atmospheric warming over Greenland, while the amplitude of high-frequency sea ice fluctuations increased through interstadials. Our findings suggest that the rapid replacement of widespread MYSI with seasonal sea ice amplified the abrupt climate warming over the course of D-O events and highlight the role of feedbacks associated with late-interstadial seasonal sea ice expansion in driving the North Atlantic ocean-climate system back to stadial conditions.

Greenland ice cores provide information about past climate. Few impurity records covering the past 2 decades exist from Greenland. Here we present results from six firn cores obtained during a 426 km long northern Greenland traverse made in 2015 between the NEEM and the EGRIP deep-drilling stations situated on the western side and eastern side of the Greenland ice sheet, respectively. The cores (9 to 14 m long) are analyzed for chemical impurities and cover time spans of 18 to 53 years (+/- 3 years) depending on local snow accumulation that decreases from west to east.The high temporal resolution allows for annual layers and seasons to be resolved. Insoluble dust, ammonium, and calcium concentrations in the six firn cores overlap, and the seasonal cycles are also similar in timing and magnitude across sites, while peroxide (H2O2) and conductivity both have spatial variations, H2O2 driven by the accumulation pattern, and conductivity likely influenced by sea salt.Overall, we determine a rather constant dust flux over the period, but in the data from recent years (1998-2015) we identify an increase in large dust particles that we ascribe to an activation of local Greenland sources. We observe an expected increase in acidity and conductivity in the mid-1970s as a result of anthropogenic emissions, followed by a decrease due to mitigation. Several volcanic horizons identified in the conductivity and acidity records can be associated with eruptions in Iceland and in the Barents Sea region. From a composite ammonium record we obtain a robust forest fire proxy associated primarily with Canadian forest fires (R = 0.49).

Nitrate (NO3-), an abundant aerosol in polar snow, is a complex environmental proxy to interpret owing to its diverse sources and susceptibility to post-depositional processes. During the last glacial period, when dust concentrations in the Antarctic ice were upto similar to 50 times than today, mineral dust appears to have a stabilizing effect on the NO3- concentration in snow. However, the mechanism leading to the stabilization remains unclear. Here, we present the new and highly resolved records of NO3- and non-sea salt calcium (nssCa(2+), a proxy for mineral dust) from the Roosevelt Island Climate Evolution (RICE) ice core. We focus on the glacial period from 83 to 26 kilo years Before Present (ka BP). The data show a statistically significant correlation between NO3- and nssCa(2+) over this period. To put our findings into a spatial context, we compare RICE data with existing records from east Antarctica (EPICA Dome C [EDC], Vostok and central Dome Fuji) and West Antarctica (West Antarctic Ice Sheet Divide Ice Core [WDC]). Spatial analysis suggests that nssCa(2+) is contributing to the effective scavenging of NO3- from the atmosphere perhaps through the formation of calcium nitrate (Ca(NO3)(2)). The geographic pattern implies that the process of Ca(NO3)(2) formation occurs during the long-distance transport of mineral dust from mid-latitude source regions by Southern Hemisphere Westerly Winds (SHWW). The data also suggest that the correlation observed at various Antarctic locations may depend on the level of dust reaching the sites from the mid-latitude sources.