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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

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.

Mercury deposition onto the Greenland Ice Sheet increased from the Last Glacial Termination to early Holocene as the North Atlantic warmed and sea ice retreated, according to an ice-core mercury record and atmospheric chemistry modelling.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.

It has been established that various anthropogenic contaminants have already reached all the world's pristine locations, including the polar regions. While some of those contaminants, such as lead and soot, are decreasing in the environment, thanks to international regulations, other novel contaminants emerge. Plastic pollution has been shown as a durable novel pollutant, and, since recently, smaller and smaller plastics particles have been identified in various environments (air, water and soil). Considerable research already exists measuring the plastics in the 5 mm to micrometre size range (microplastics). However, far less is known about the plastics debris that fragmented to the sub-micrometre size (nanoplastics). As these small particles are light, it is expected that they have already reached the most remote places on Earth, e.g. transported across the globe by air movement. In this work, we used a novel method based on Thermal Desorption – Proton Transfer Reaction – Mass Spectrometry (TD-PTR-MS) to detect and measure nanoplastics of different types in the water sampled from a Greenland firn core (T2015-A5) and a sea ice core from Antarctica. We identify polyethylene (PE), polypropylene (PP), polyethylene terephthalate (PET), polystyrene (PS), polyvinyl chloride (PVC), and Tire wear nanoparticles in the 14 m deep Greenland firn core and PE, PP and PET in sea ice from Antarctica. Nanoplastics mass concentrations were on average 13.2 ng/mL for Greenland firn samples and 52.3 ng/mL for Antarctic sea ice. We further discuss the possible sources of nanoplastics that we found at these remote locations, which likely involve complex processes of plastic circulation (emission from both land and sea surface, atmospheric and marine circulation).

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.

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.

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.

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.

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).

A new study finds that the North East Greenland ice stream is not as stable as previously thought and that this will affect its future evolution.Mass loss near the ice-sheet margin is evident from remote sensing as frontal retreat and increases in ice velocities. Velocities in the ice sheet interior are orders of magnitude smaller, making it challenging to detect velocity change. Here, we analyze a 35-year record of remotely sensed velocities, and a 6-year record of repeated GPS observations, at the East Greenland Ice-core Project (EastGRIP), located in the middle of the Northeast-Greenland Ice Stream (NEGIS). We find that the shear margins of NEGIS are accelerating, indicating a widening of the ice stream. We demonstrate that the widening of the ice stream is unlikely to be a response to recent changes at the outlets of NEGIS. Modelling indicates that the observed spatial fingerprint of acceleration is more consistent with a softening of the shear margin, e.g. due to evolving fabric or temperature, than a response to external forcing at the surface or bed.

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).

A new study finds that the North East Greenland ice stream is not as stable as previously thought and that this will affect its future evolution.Mass loss near the ice-sheet margin is evident from remote sensing as frontal retreat and increases in ice velocities. Velocities in the ice sheet interior are orders of magnitude smaller, making it challenging to detect velocity change. Here, we analyze a 35-year record of remotely sensed velocities, and a 6-year record of repeated GPS observations, at the East Greenland Ice-core Project (EastGRIP), located in the middle of the Northeast-Greenland Ice Stream (NEGIS). We find that the shear margins of NEGIS are accelerating, indicating a widening of the ice stream. We demonstrate that the widening of the ice stream is unlikely to be a response to recent changes at the outlets of NEGIS. Modelling indicates that the observed spatial fingerprint of acceleration is more consistent with a softening of the shear margin, e.g. due to evolving fabric or temperature, than a response to external forcing at the surface or bed.

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 kab2k), 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 disti

It has been established that various anthropogenic contaminants have already reached all the world's pristine locations, including the polar regions. While some of those contaminants, such as lead and soot, are decreasing in the environment, thanks to international regulations, other novel contaminants emerge. Plastic pollution has been shown as a durable novel pollutant, and, since recently, smaller and smaller plastics particles have been identified in various environments (air, water and soil). Considerable research already exists measuring the plastics in the 5 mm to micrometre size range (microplastics). However, far less is known about the plastics debris that fragmented to the sub-micrometre size (nanoplastics). As these small particles are light, it is expected that they have already reached the most remote places on Earth, e.g. transported across the globe by air movement. In this work, we used a novel method based on Thermal Desorption - Proton Transfer Reaction - Mass Spectrometry (TD-PTR-MS) to detect and measure nanoplastics of different types in the water sampled from a Greenland firn core (T2015-A5) and a sea ice core from Antarctica. We identify polyethylene (PE), poly-propylene (PP), polyethylene terephthalate (PET), polystyrene (PS), polyvinyl chloride (PVC), and Tire wear nanoparticles in the 14 m deep Greenland firn core and PE, PP and PET in sea ice from Antarctica. Nanoplastics mass concentrations were on average 13.2 ng/mL for Greenland firn samples and 52.3 ng/mL for Antarctic sea ice. We further discuss the possible sources of nanoplastics that we found at these remote locations, which likely involve complex processes of plastic circulation (emission from both land and sea surface, atmospheric and marine circulation).

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

It has been established that various anthropogenic contaminants have already reached all the world's pristine locations, including the polar regions. While some of those contaminants, such as lead and soot, are decreasing in the environment, thanks to international regulations, other novel contaminants emerge. Plastic pollution has been shown as a durable novel pollutant, and, since recently, smaller and smaller plastics particles have been identified in various environments (air, water and soil). Considerable research already exists measuring the plastics in the 5 mm to micrometre size range (microplastics). However, far less is known about the plastics debris that fragmented to the sub-micrometre size (nanoplastics). As these small particles are light, it is expected that they have already reached the most remote places on Earth, e.g. transported across the globe by air movement. In this work, we used a novel method based on Thermal Desorption - Proton Transfer Reaction - Mass Spectrometry (TD-PTR-MS) to detect and measure nanoplastics of different types in the water sampled from a Greenland firn core (T2015-A5) and a sea ice core from Antarctica. We identify polyethylene (PE), poly-propylene (PP), polyethylene terephthalate (PET), polystyrene (PS), polyvinyl chloride (PVC), and Tire wear nanoparticles in the 14 m deep Greenland firn core and PE, PP and PET in sea ice from Antarctica. Nanoplastics mass concentrations were on average 13.2 ng/mL for Greenland firn samples and 52.3 ng/mL for Antarctic sea ice. We further discuss the possible sources of nanoplastics that we found at these remote locations, which likely involve complex processes of plastic circulation (emission from both land and sea surface, atmospheric and marine circulation).

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 kab2k), 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 disti

It has been established that various anthropogenic contaminants have already reached all the world's pristine locations, including the polar regions. While some of those contaminants, such as lead and soot, are decreasing in the environment, thanks to international regulations, other novel contaminants emerge. Plastic pollution has been shown as a durable novel pollutant, and, since recently, smaller and smaller plastics particles have been identified in various environments (air, water and soil). Considerable research already exists measuring the plastics in the 5 mm to micrometre size range (microplastics). However, far less is known about the plastics debris that fragmented to the sub-micrometre size (nanoplastics). As these small particles are light, it is expected that they have already reached the most remote places on Earth, e.g. transported across the globe by air movement. In this work, we used a novel method based on Thermal Desorption – Proton Transfer Reaction – Mass Spectrometry (TD-PTR-MS) to detect and measure nanoplastics of different types in the water sampled from a Greenland firn core (T2015-A5) and a sea ice core from Antarctica. We identify polyethylene (PE), polypropylene (PP), polyethylene terephthalate (PET), polystyrene (PS), polyvinyl chloride (PVC), and Tire wear nanoparticles in the 14 m deep Greenland firn core and PE, PP and PET in sea ice from Antarctica. Nanoplastics mass concentrations were on average 13.2 ng/mL for Greenland firn samples and 52.3 ng/mL for Antarctic sea ice. We further discuss the possible sources of nanoplastics that we found at these remote locations, which likely involve complex processes of plastic circulation (emission from both land and sea surface, atmospheric and marine circulation)., SCOPUS: ar.j, info:eu-repo/semantics/published

There are enormous costs involved in transporting snow and ice samples to home laboratories for “simple” analyses in order to constrain annual layer thicknesses and identify accumulation rates of specific sites. It is well known that depositional noise, incurred from factors such as wind drifts, seasonally biased deposition and melt layers can influence individual snow and firn records and that multiple cores are required to produce statistically robust time series. Thus, at many sites, core samples are measured in the field for densification, but the annual accumulation and the content of chemical impurities are often represented by just one core to reduce transport costs. We have developed a portable “lightweight in situ analysis” (LISA) box for ice, firn and snow analysis that is capable of constraining annual layers through the continuous flow analysis of meltwater conductivity and hydrogen peroxide under field conditions. The box can run using a small gasoline generator and weighs less than 50 kg. The LISA box was tested under field conditions at the East Greenland Ice-core Project (EastGRIP) deep ice core drilling site in northern Greenland. Analysis of the top 2 m of snow from seven sites in northern Greenland allowed the reconstruction of regional snow accumulation patterns for the 2015–2018 period (summer to summer).

The climate of the sub-Antarctic is important in understanding the environmental conditions of Antarctica and the Southern Ocean. However, regional climate proxy records from this region are scarce. In this study, we present the stable water isotopes, major ion chemistry, and dust records from the first ice core from the (sub-)Antarctic Young Island. We present and discuss various dating approaches based on commonly used ice core proxies, such as stable water isotopes and seasonally deposited ions, together with site-specific characteristics such as melt layers. The dating approaches are compared with estimated precipitation rates from reanalysis data (ERA5) and volcanic cryptotephra shards likely presenting an absolute tie point from a 2001 CE eruption on neighboring Sturge Island. The resulting ice core age scale spans the period 2016 to 1995, with an uncertainty of ±2 years.

There are enormous costs involved in transporting snow and ice samples to home laboratories for “simple” analyses in order to constrain annual layer thicknesses and identify accumulation rates of specific sites. It is well known that depositional noise, incurred from factors such as wind drifts, seasonally biased deposition and melt layers can influence individual snow and firn records and that multiple cores are required to produce statistically robust time series. Thus, at many sites, core samples are measured in the field for densification, but the annual accumulation and the content of chemical impurities are often represented by just one core to reduce transport costs. We have developed a portable “lightweight in situ analysis” (LISA) box for ice, firn and snow analysis that is capable of constraining annual layers through the continuous flow analysis of meltwater conductivity and hydrogen peroxide under field conditions. The box can run using a small gasoline generator and weighs less than 50 kg. The LISA box was tested under field conditions at the East Greenland Ice-core Project (EastGRIP) deep ice core drilling site in northern Greenland. Analysis of the top 2 m of snow from seven sites in northern Greenland allowed the reconstruction of regional snow accumulation patterns for the 2015–2018 period (summer to summer).

There are enormous costs involved in transporting snow and ice samples to home laboratories for "simple"analyses in order to constrain annual layer thicknesses and identify accumulation rates of specific sites. It is well known that depositional noise, incurred from factors such as wind drifts, seasonally biased deposition and melt layers can influence individual snow and firn records and that multiple cores are required to produce statistically robust time series. Thus, at many sites, core samples are measured in the field for densification, but the annual accumulation and the content of chemical impurities are often represented by just one core to reduce transport costs. We have developed a portable "lightweight in situ analysis"(LISA) box for ice, firn and snow analysis that is capable of constraining annual layers through the continuous flow analysis of meltwater conductivity and hydrogen peroxide under field conditions. The box can run using a small gasoline generator and weighs less than 50 kg. The LISA box was tested under field conditions at the East Greenland Ice-core Project (EastGRIP) deep ice core drilling site in northern Greenland. Analysis of the top 2 m of snow from seven sites in northern Greenland allowed the reconstruction of regional snow accumulation patterns for the 2015-2018 period (summer to summer).

The climate of the sub-Antarctic is important in understanding the environmental conditions of Antarctica and the Southern Ocean. However, regional climate proxy records from this region are scarce. In this study, we present the stable water isotopes, major ion chemistry, and dust records from the first ice core from the (sub-)Antarctic Young Island. We present and discuss various dating approaches based on commonly used ice core proxies, such as stable water isotopes and seasonally deposited ions, together with site-specific characteristics such as melt layers. The dating approaches are compared with estimated precipitation rates from reanalysis data (ERA5) and volcanic cryptotephra shards likely presenting an absolute tie point from a 2001 CE eruption on neighboring Sturge Island. The resulting ice core age scale spans the period 2016 to 1995, with an uncertainty of ±2 years.

There are enormous costs involved in transporting snow and ice samples to home laboratories for "simple"analyses in order to constrain annual layer thicknesses and identify accumulation rates of specific sites. It is well known that depositional noise, incurred from factors such as wind drifts, seasonally biased deposition and melt layers can influence individual snow and firn records and that multiple cores are required to produce statistically robust time series. Thus, at many sites, core samples are measured in the field for densification, but the annual accumulation and the content of chemical impurities are often represented by just one core to reduce transport costs. We have developed a portable "lightweight in situ analysis"(LISA) box for ice, firn and snow analysis that is capable of constraining annual layers through the continuous flow analysis of meltwater conductivity and hydrogen peroxide under field conditions. The box can run using a small gasoline generator and weighs less than 50 kg. The LISA box was tested under field conditions at the East Greenland Ice-core Project (EastGRIP) deep ice core drilling site in northern Greenland. Analysis of the top 2 m of snow from seven sites in northern Greenland allowed the reconstruction of regional snow accumulation patterns for the 2015-2018 period (summer to summer).

Sea ice plays a pivotal role in Earth's climate and its past reconstruction is crucial to investigate the connections and feedbacks with the other components of the climate system. Among the available archives that store information of past sea ice are marine and ice cores. Recent studies on the IP 25 biomarker extracted from marine sediments has shown great skill to infer past changes of Arctic sea ice. In ice matrixes, sodium, bromine and iodine have shown potential to store the fingerprint of sea ice presence. The development of an unambiguous sea ice proxy from ice cores, however, has proven to be a challenging task especially in the Arctic realm.In this work we analyze the sodium, bromine and iodine records in the RECAP ice core, coastal eastern Greenland, to investigate the sea ice variability in the northern North Atlantic Ocean through the last 11,000 years of the current interglacial, i.e. the Holocene. We compare the RECAP records with marine sea ice proxy records available from the northern North Atlantic.We suggest that RECAP sodium concentrations can be associated with variability of sea ice extent, while the bromine-to-sodium ratios and iodine are associated respectively with seasonal sea ice and bioproductivity from open ocean and fresh sea ice surfaces.According to our interpretation, we find that sea ice was at its lowest extent and seasonal in nature during the early Holocene in all regions of the North Atlantic. Increasing sea ice signals are seen from ca. 8-9 ka b2k, in line with long-term Holocene cooling. The increasing sea ice trend appears uninterrupted in the Fram Strait and North Iceland while reaching a maximum ca. 5 ka b2k in the East Greenland region. Sea ice modifications during the last 5000 years display great variability in East Greenland with intermediate conditions between the early and mid Holocene, possibly associated with local fjord dynamics. The last sea ice maximum was reached across all regions 1000 y

The climate of the sub-Antarctic is important in understanding the environmental conditions of Antarctica and the Southern Ocean. However, regional climate proxy records from this region are scarce. In this study, we present the stable water isotopes, major ion chemistry, and dust records from the first ice core from the (sub-)Antarctic Young Island. We present and discuss various dating approaches based on commonly used ice core proxies, such as stable water isotopes and seasonally deposited ions, together with site-specific characteristics such as melt layers. The dating approaches are compared with estimated precipitation rates from reanalysis data (ERA5) and volcanic cryptotephra shards likely presenting an absolute tie point from a 2001 CE eruption on neighboring Sturge Island. The resulting ice core age scale spans the period 2016 to 1995, with an uncertainty of +/- 2 years.

As the intricacies of paleoclimate dynamics are explored, it is becoming understood that sea-ice variability can instigate, or contribute to, climate change instabilities commonly described as "tipping points". Compared to ice sheets and circulating ocean currents, sea-ice is ephemeral and continentalscale changes to sea ice cover occur seasonally. Sea-ice greatly influences polar albedo, atmosphere-ocean gas exchange and vertical mixing of polar ocean masses. Major changes in sea ice distribution and thickness have been invoked as drivers of deglaciations as well as stadial climate variability described in Greenland climate records as "Dansgaard-Oeschger" cycles and described in Antarctic climate records as "Antarctic Isotopic Maxima".The role of halogens in polar atmospheric chemistry has been studied intensively over the past few decades. This research has been driven by the role of bromine, primarily as gas-phase bromine monoxide (BrO), which exerts a key control on polar tropospheric ozone concentrations. Initial findings led to the discovery of boundary-layer self-catalyzing heterogeneous bromine reactions fed by sunlight and ozone, known as bromine explosions. First-year sea-ice and blowing snow have been identified as key components for this heterogeneous bromine recycling in the polar boundary layer. This understanding of polar halogen chemistry - supported by an expanding body of observations and modeling - has formed the basis for investigating quantitative links between halogen concentrations in the polar atmospheric boundary layer and sea-ice presence and/or extent.Despite the clear importance of sea-ice in paleoclimate research, the ice core community lacks a conservative and quantitative proxy for sea-ice extent. The most commonly applied proxy, methanesulphonic acid (MSA), is volatile and has not been demonstrated reliably for ice core records extending beyond the last few centuries. Sodium has also been applied to reconstruct sea-ic

Biomass burning influences global atmospheric chemistry by releasing greenhouse gases and climate-forcing aerosols. There is controversy about the magnitude and timing of Holocene changes in biomass burning emissions from millennial to centennial timescales and, in particular, about the possible impact of ancient civilizations. Here we present a 5 kyr record of fire activity proxies levoglucosan, black carbon, and ammonium measured in the RECAP (Renland ice cap) ice core, drilled in coastal eastern Greenland, and therefore affected by processes occurring in the high North Atlantic region. Levoglucosan and ammonium fluxes are high from 5 to 4.5 kyr BP (thousand years before 2000 CE) followed by an abrupt decline, possibly due to monotonic decline in Northern Hemisphere summer insolation. Levoglucosan and black carbon show an abrupt decline at 1.1 kyr BP, suggesting a decline in the wildfire regime in Iceland due to the extensive land clearing caused by Viking colonizers. All fire proxies reach a minimum during the second half of the last century, after which levoglucosan and ammonium fluxes increase again, in particular over the last 200 years. We find that the fire regime reconstructed from RECAP fluxes seems mainly related to climatic changes; however over the last mil-lennium human activities might have influenced wildfire frequency/occurrence substantially.