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Results from six firn cores obtained during a 426 km long northern Greenland traverse in 2015 between the NEEM and the EGRIP deep drilling stations situated on the Western and Eastern side of the Greenland ice sheet, respectively. The cores (9 to 14 m long) are analysed for chemical impurities by means of Continuous Flow Analysis (CFA); Insoluble dust, ammonium, calcium, acid, conductivity and peroxide. The data was dated by means of annual layer counting of mainly peroxide supplemented by calcium seasonal cycles and spans 18 to 53 years (±3 yrs) depending on local snow accumulation that decreases from west to east. Insoluble dust, ammonium, and calcium concentrations in the 6 firn cores overlap, and also the seasonal cycles are similar in timing and magnitude across sites, while peroxide (H2O2) and conductivity both have spatial variations. H2O2 is driven by the accumulation pattern and conductivity is likely influenced by sea salt. Data is published as part of Kjær et al. 2022, Climate of the past, https://doi.org/10.5194/cp-2021-99

We combine consistently dated benthic carbon isotopic records distributed over the entire Atlantic Ocean with numerical simulations performed by a glacial configuration of the Norwegian Earth System Model with active ocean biogeochemistry, in order to interpret the observed Cibicides δ13C changes at the stadial-interstadial transition corresponding to the end of Heinrich Stadial 4 (HS4) in terms of ocean circulation and remineralization changes. We show that the marked increase in Cibicides δ13C observed at the end of HS4 between ~2000 and 4200 m in the Atlantic can be explained by changes in nutrient concentrations as simulated by the model in response to the halting of freshwater input in the high latitude glacial North Atlantic. Our model results show that this Cibicides δ13C signal is associated with changes in the ratio of southern-sourced (SSW) versus northern-sourced (NSW) water masses at the core sites, whereby SSW is replaced by NSW as a consequence of the resumption of deep water formation in the northern North Atlantic and Nordic Seas after the freshwater input is halted. Our results further suggest that the contribution of ocean circulation changes to this signal increases from ~40 % at 2000 m to ~80 % at 4000 m. Below ~4200 m, the model shows little ocean circulation change but an increase in remineralization across the transition marking the end of HS4. The simulated lower remineralization during stadials than interstadials is particularly pronounced in deep subantarctic sites, in agreement with the decrease in the export production of carbon to the deep Southern Ocean during stadials found in previous studies.

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).

The role of icebergs in narrow fjords hosting marine terminating glaciers in Greenland is poorly understood, even though icebergs provide a substantial freshwater flux that can exceed the subglacial discharge. Iceberg melt is distributed at depth, contributing to fjord stratification, thus impacting melt and dynamics of the glacier front. We model the high-silled Ilulissat Icefjord in Western Greenland with the MITgcm ocean model, using the IceBerg package to study the effect of icebergs on fjord properties, and compare our results with available observations from 2014. We find the subglacial discharge plume to be the primary driver of the seasonality of circulation, glacier melt and iceberg melt. Icebergs are necessary to include to correctly understand the properties of Ilulissat Icefjord, since they modify the fjord in three main ways: First, icebergs cool and freshen the water column within their vertical extent; Second, icebergs depress the neutral buoyancy depth of the plume and the outflow route of glacially modified water; Third, icebergs modify the deep basin, below their vertical extent, due to both increased entrainment of glacially modified water into the fjord, and iceberg modification of the incoming ambient water. Furthermore, the depressed neutral buoyancy depth of the plume limits melt to the deep section of the front of Sermeq Kujalleq (Jakobshavn Isbræ) even during peak summer, and thus promotes undercutting. We postulate that the impact of icebergs on the neutral buoyancy depth of the plume is a key mechanism connecting iceberg melange and glacier calving, independent of mechanical support.

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.

Tropospheric ozone (O3) concentrations depend on a combination of hemispheric, regional, and local-scale processes. Estimates of how much O3 is produced locally vs. transported from further afield are essential in air quality management and regulatory policies. Here, a tagged-ozone mechanism within the Weather Research and Forecasting model coupled with chemistry (WRF-Chem) is used to quantify the contributions to surface O3 in the UK from anthropogenic nitrogen oxide (NOx) emissions from inside and outside the UK during May–August 2015. The contribution of the different source regions to three regulatory O3 metrics is also examined. It is shown that model simulations predict the concentration and spatial distribution of surface O3 with a domain-wide mean bias of −3.7 ppbv. Anthropogenic NOx emissions from the UK and Europe account for 13 % and 16 %, respectively, of the monthly mean surface O3 in the UK, as the majority (71 %) of O3 originates from the hemispheric background. Hemispheric O3 contributes the most to concentrations in the north and the west of the UK with peaks in May, whereas European and UK contributions are most significant in the east, south-east, and London, i.e. the UK's most populated areas, intensifying towards June and July. Moreover, O3 from European sources is generally transported to the UK rather than produced in situ. It is demonstrated that more stringent emission controls over continental Europe, particularly in western Europe, would be necessary to improve the health-related metric MDA8 O3 above 50 and 60 ppbv. Emission controls over larger areas, such as the Northern Hemisphere, are instead required to lessen the impacts on ecosystems as quantified by the AOT40 metric.

Permafrost is perennially frozen ground, such as soil, rock, and ice. In permafrost regions, plant and microbial life persists primarily in the near-surface soil that thaws every summer, called the ‘active layer’ (Figure 20). The cold and wet conditions in many permafrost regions limit decomposition of organic matter. In combination with soil mixing processes caused by repeated freezing and thawing, this has led to the accumulation of large stocks of soil organic carbon in the permafrost zone over multi-millennial timescales. As the climate warms, permafrost carbon could be highly vulnerable to climatic warming. Permafrost occurs primarily in high latitudes (e.g. Arctic and Antarctic) and at high elevation (e.g. Tibetan Plateau, Figure 21). The thickness of permafrost varies from less than 1 m (in boreal peatlands) to more than 1 500 m (in Yakutia). The coldest permafrost is found in the Transantarctic Mountains in Antarctica (−36°C) and in northern Canada for the Northern Hemisphere (-15°C; Obu et al., 2019, 2020). In contrast, some of the warmest permafrost occurs in peatlands in areas with mean air temperatures above 0°C. Here permafrost exists because thick peat layers insulate the ground during the summer. Most of the permafrost existing today formed during cold glacials (e.g. before 12 000 years ago) and has persisted through warmer interglacials. Some shallow permafrost (max 30–70m depth) formed during the Holocene (past 5000 years) and some even during the Little Ice Age from 400–150 years ago. There are few extensive regions suitable for row crop agriculture in the permafrost zone. Additionally, in areas where large-scale agriculture has been conducted, ground destabilization has been common. Surface disturbance such as plowing or trampling of vegetation can alter the thermal regime of the soil, potentially triggering surface subsidence or abrupt collapse. This may influence soil hydrology, nutrient cycling, and organic matter storage. These changes often have acute and negative consequences for continued agricultural use of such landscapes. Thus, row-crop agriculture could have a negative impact on permafrost (e.g. Grünzweig et al., 2014). Conversely, animal husbandry is widespread in the permafrost zone, including horses, cattle, and reindeer.

Greenland ice cores provide information about past climate. However, the number of firn and ice cores from Greenland are limited and thus the spatial variability of the chemical impurities used as proxies is largely unconstrained. Furthermore, few impurity records covering the past two decades exist from Greenland. We have by means of Continuous Flow analysis investigated 6 shallow firn cores obtained in Northern Greenland as part of the NEEM to EastGRIP traverse in 2015. The oldest reach back to 1966. The annual mean and quartiles of the insoluble dust, ammonium, and calcium concentrations in the 6 firn cores spanning a distance of 426 km overlap, and also the seasonal cycles have similar peaks in timing and magnitude across sites. Peroxide (H2O2) is accumulation dependent and varies from site to site and conductivity, likely influenced by sea salts, also vary spatially. The temporal variability of the records is further assessed. We find no evidence for increases in total dust concentration, but find an increase in the large dust particle fluxes that we contribute to an activation of Greenland local sources in the recent years (1998–2015). We observe the expected acid and conductivity increase in the mid 70’s as a result of anthropogenic contamination and the following decrease due to mitigation. After detrending using the five year average the conductivity and acid records several volcanic horizons were identified and associated with Icelandic eruptions and volcanic eruptions in the Barents sea region. By creating a composite based on excess ammonium compared to the five year running average, we obtain a robust forest fire proxy associated primarily with Canadian forest fires (R = 0.51). We also note that the peak ammonium in the individual firn cores appear more scattered between cores than the peak volcanic layers, suggesting that the forest fire signal is more dispersed in the atmosphere than the acid from volcanic eruptions.

Lakes in permafrost regions are dynamic landscape components and play an important role for climate change feedbacks. Lake processes such as mineralization and flocculation of dissolved organic carbon (DOC), one of the main carbon fractions in lakes, contribute to the greenhouse effect and are part of the global carbon cycle. These processes are in the focus of climate research, but studies so far are limited to specific study regions. In our synthesis, we analyzed 2167 water samples from 1833 lakes across the Arctic in permafrost regions of Alaska, Canada, Greenland, and Siberia to provide first pan-Arctic insights for linkages between DOC concentrations and the environment. Using published data and unpublished datasets from the author team, we report regional DOC differences linked to latitude, permafrost zones, ecoregions, geology, near-surface soil organic carbon contents, and ground ice classification of each lake region. The lake DOC concentrations in our dataset range from 0 to 1130 mg L−1 (10.8 mg L−1 median DOC concentration). Regarding the permafrost regions of our synthesis, we found median lake DOC concentrations of 12.4 mg L−1 (Siberia), 12.3 mg L−1 (Alaska), 10.3 mg L−1 (Greenland), and 4.5 mg L−1 (Canada). Our synthesis shows a significant relationship between lake DOC concentration and lake ecoregion. We found higher lake DOC concentrations at boreal permafrost sites compared to tundra sites. We found significantly higher DOC concentrations in lakes in regions with ice-rich syngenetic permafrost deposits (yedoma) compared to non-yedoma lakes and a weak but significant relationship between soil organic carbon content and lake DOC concentration as well as between ground ice content and lake DOC. Our pan-Arctic dataset shows that the DOC concentration of a lake depends on its environmental properties, especially on permafrost extent and ecoregion, as well as vegetation, which is the most important driver of lake DOC in this study. This new dataset will be fundamental to quantify a pan-Arctic lake DOC pool for estimations of the impact of lake DOC on the global carbon cycle and climate change.

This study presents simulations of Greenland surface melt for the Eemian interglacial period (∼130 000 to 115 000 years ago) derived from regional climate simulations with a coupled surface energy balance model. Surface melt is of high relevance due to its potential effect on ice core observations, e.g., lowering the preserved total air content (TAC) used to infer past surface elevation. An investigation of surface melt is particularly interesting for warm periods with high surface melt, such as the Eemian interglacial period. Furthermore, Eemian ice is the deepest and most compressed ice preserved on Greenland, resulting in our inability to identify melt layers visually. Therefore, simulating Eemian melt rates and associated melt layers is beneficial to improve the reconstruction of past surface elevation. Estimated TAC, based on simulated melt during the Eemian, could explain the lower TAC observations. The simulations show Eemian surface melt at all deep Greenland ice core locations and an average of up to ∼30 melt days per year at Dye-3, corresponding to more than 600 mm water equivalent (w.e.) of annual melt. For higher ice sheet locations, between 60 and 150 mmw.e.yr-1 on average are simulated. At the summit of Greenland, this yields a refreezing ratio of more than 25 % of the annual accumulation. As a consequence, high melt rates during warm periods should be considered when interpreting Greenland TAC fluctuations as surface elevation changes. In addition to estimating the influence of melt on past TAC in ice cores, the simulated surface melt could potentially be used to identify coring locations where Greenland ice is best preserved.