Helle A. Kjær

Greenland 2012 melt event effects on CryoSat‐2 radar altimetry

CryoSat-2 data are used to study elevation changes over an area in the interior part of the Greenland Ice Sheet during the extreme melt event in July 2012. The penetration of the radar signal into dry snow depends heavily on the snow stratigraphy, and the rapid formation of refrozen ice layers can bias the surface elevations obtained from radar altimetry. We investigate the change in CryoSat-2 waveforms and elevation estimates over the melt event and interpret the findings by comparing in situ surface and snow pit observations from the North Greenland Eemian Ice Drilling Project camp. The investigation shows a major transition of scattering properties around the area, and an apparent elevation increase of 56 ± 26 cm is observed in reprocessed CryoSat-2 data. We suggest that this jump in elevation can be explained by the formation of a refrozen melt layer that raised the reflective surface, introducing a positive elevation bias.

Organic phosphorus in the terrestrial environment: a perspective on the state of the art and future priorities

BackgroundThe dynamics of phosphorus (P) in the environment is important for regulating nutrient cycles in natural and managed ecosystems and an integral part in assessing biological resilience against environmental change. Organic P (Po) compounds play key roles in biological and ecosystems function in the terrestrial environment being critical to cell function, growth and reproduction.ScopeWe asked a group of experts to consider the global issues associated with Po in the terrestrial environment, methodological strengths and weaknesses, benefits to be gained from understanding the Po cycle, and to set priorities for Po research.ConclusionsWe identified seven key opportunities for Po research including: the need for integrated, quality controlled and functionally based methodologies; assessment of stoichiometry with other elements in organic matter; understanding the dynamics of Po in natural and managed systems; the role of microorganisms in controlling Po cycles; the implications of nanoparticles in the environment and the need for better modelling and communication of the research. Each priority is discussed and a statement of intent for the Po research community is made that highlights there are key contributions to be made toward understanding biogeochemical cycles, dynamics and function of natural ecosystems and the management of agricultural systems.

Determination of 129I in Arctic snow by a novel analytical approach using IC-ICP-SFMS

The environmental radiation background has increased in the last century due to human nuclear activities and in this context 129I may be used to evaluate the anthropogenic contribution to global nuclear contamination. We present a fast and novel method for iodine-129 measurements. Coupling ion chromatography and inductively coupled plasma sector field mass spectrometry (IC-ICP-SFMS) allows the determination of iodine-129 at picogram per gram levels. The capability of the Dionex IONPAC® AS16 column to retain iodine species in the absence of NaOH has been used to pre-concentrate 5 mL samples. Although 129I suffers from isobaric spectral interference due to the presence of 129Xe, the IC-ICP-SFMS technique allows 129I to be determined by removing all other isobaric interferents. Furthermore, the 129Xe interference is sufficiently small and stable to be treated as a background correction. This strategy permits the evaluation of 129I speciation at sub-picogram per gram levels with a limit of detection (LOD) of 0.7 pg g−1. Thus the range of possible applications of this technique is expanded to low-concentration environmental samples such as polar snow. Preliminary results obtained from Greenland (NEEM) snow pit samples confirm its applicability in environmental research.

Continuous flow analysis method for determination of dissolved reactive phosphorus in ice cores.

Phosphorus (P) is an essential macronutrient for all living organisms. Phosphorus is often present in nature as the soluble phosphate ion PO4(3-) and has biological, terrestrial, and marine emission sources. Thus PO4(3-) detected in ice cores has the potential to be an important tracer for biological activity in the past. In this study a continuous and highly sensitive absorption method for detection of dissolved reactive phosphorus (DRP) in ice cores has been developed using a molybdate reagent and a 2-m liquid waveguide capillary cell (LWCC). DRP is the soluble form of the nutrient phosphorus, which reacts with molybdate. The method was optimized to meet the low concentrations of DRP in Greenland ice, with a depth resolution of approximately 2 cm and an analytical uncertainty of 1.1 nM (0.1 ppb) PO4(3-). The method has been applied to segments of a shallow firn core from Northeast Greenland, indicating a mean concentration level of 2.74 nM (0.26 ppb) PO4(3-) for the period 1930-2005 with a standard deviation of 1.37 nM (0.13 ppb) PO4(3-) and values reaching as high as 10.52 nM (1 ppb) PO4(3-). Similar levels were detected for the period 1771-1823. Based on impurity abundances, dust and biogenic particles were found to be the most likely sources of DRP deposited in Northeast Greenland.

A 2700-year annual timescale and accumulation history for an ice core from Roosevelt Island, West Antarctica

We present a 2700-year annually resolved chronology and snow accumulation history for the Roosevelt Island Climate Evolution (RICE) ice core, Ross Ice Shelf, West Antarctica. The core adds information on past accumulation changes in an otherwise poorly constrained sector of Antarctica. The timescale was constructed by identifying annual cycles in high-resolution impurity records, and it constitutes the top part of the Roosevelt Island Ice Core Chronology 2017 (RICE17). Validation by volcanic and methane matching to the WD2014 chronology from the WAIS Divide ice core shows that the two timescales are in excellent agreement. In a companion paper, gas matching to WAIS Divide is used to extend the timescale for the deeper part of the core in which annual layers cannot be identified. Based on the annually resolved timescale, we produced a record of past snow accumulation at Roosevelt Island. The accumulation history shows that Roosevelt Island experienced slightly increasing accumulation rates between 700 BCE and 1300 CE, with an average accumulation of 0.25± 0.02 m water equivalent (w.e.) per year. Since 1300 CE, trends in the accumulation rate have been consistently negative, with an acceleration in the rate of decline after the mid-17th century. The current accumulation rate at Roosevelt Island is 0.210±0.002 m w.e. yr−1 (average since 1965 CE, ±2σ ), and it is rapidly declining with a trend corresponding to 0.8 mm yr−2. The decline observed since the mid-1960s is 8 times faster than the long-term decreasing trend taking place over the previous centuries, with decadal mean accumulation rates consistently being below average. Previous research has shown a strong link between Roosevelt Island accumulation rates and the location and intensity of the Amundsen Sea Low, which has a significant impact on regional sea-ice extent. The decrease in accumulation rates at Roosevelt Island may therefore be explained in terms of a recent strengthening of the ASL and the expansion of sea ice in the eastern Ross Sea. The start of the rapid decrease in RICE accumulation rates observed in 1965 CE may Published by Copernicus Publications on behalf of the European Geosciences Union. 752 M. Winstrup et al.: Timescale and accumulation history for an ice core from Roosevelt Island thus mark the onset of significant increases in regional seaice extent.

Greenland records of aerosol source and atmospheric lifetime changes from the Eemian to the Holocene

The Northern Hemisphere experienced dramatic changes during the last glacial, featuring vast ice sheets and abrupt climate events, while high northern latitudes during the last interglacial (Eemian) were warmer than today. Here we use high-resolution aerosol records from the Greenland NEEM ice core to reconstruct the environmental alterations in aerosol source regions accompanying these changes. Separating source and transport effects, we find strongly reduced terrestrial biogenic emissions during glacial times reflecting net loss of vegetated area in North America. Rapid climate changes during the glacial have little effect on terrestrial biogenic aerosol emissions. A strong increase in terrestrial dust emissions during the coldest intervals indicates higher aridity and dust storm activity in East Asian deserts. Glacial sea salt aerosol emissions in the North Atlantic region increase only moderately (50%), likely due to sea ice expansion. Lower aerosol concentrations in Eemian ice compared to the Holocene are mainly due to shortened atmospheric residence time, while emissions changed little.Past climate changes in Greenland ice were accompanied by large aerosol concentration changes. Here, the authors show that by correcting for transport effects, reliable source changes for biogenic aerosol from North America, sea salt aerosol from the North Atlantic, and dust from East Asian deserts can be derived.

Rapid increase in atmospheric iodine levels in the North Atlantic since the mid-20th century

Atmospheric iodine causes tropospheric ozone depletion and aerosol formation, both of which have significant climate impacts, and is an essential dietary element for humans. However, the evolution of atmospheric iodine levels at decadal and centennial scales is unknown. Here, we report iodine concentrations in the RECAP ice-core (coastal East Greenland) to investigate how atmospheric iodine levels in the North Atlantic have evolved over the past 260 years (1750–2011), this being the longest record of atmospheric iodine in the Northern Hemisphere. The levels of iodine tripled from 1950 to 2010. Our results suggest that this increase is driven by anthropogenic ozone pollution and enhanced sub-ice phytoplankton production associated with the recent thinning of Arctic sea ice. Increasing atmospheric iodine has accelerated ozone loss and has considerably enhanced iodine transport and deposition to the Northern Hemisphere continents. Future climate and anthropogenic forcing may continue to amplify oceanic iodine emissions with potentially significant health and environmental impacts at global scale.Despite its chemical importance, the evolution of atmospheric iodine concentrations over time is unknown. Here, the authors show that North Atlantic atmospheric iodine levels have tripled since 1950, and propose ozone pollution and enhanced biological production Arctic sea ice thinning as a primary driver.

120,000 year record of sea ice in the North Atlantic

Although it has been demonstrated that the speed and magnitude of the recent Arctic sea ice decline is unprecedented for the past 1450 years, few records are available to provide a paleoclimate context for Arctic sea ice extent. Bromine enrichment in ice cores has been suggested to indicate the extent of newly formed sea ice areas. Despite the similarities among sea ice indicators and ice core bromine enrichment records, uncertainties still exist regarding the quantitative linkages between bromine reactive chemistry and the first-year sea ice surfaces. Here we present a 120 000-year record of bromine enrichment from the RECAP (REnland ice CAP) ice core, coastal east Greenland, and interpret it as a record of first-year sea ice. We compare it to existing sea ice records from marine cores and tentatively reconstruct past sea ice conditions in the North Atlantic as far north as the Fram Strait (50–85 N). Our interpretation implies that during the last deglaciation, the transition from multi-year to first-year sea ice started at ∼ 17.5 ka, synchronously with sea ice reductions observed in the eastern Nordic Seas and with the increase in North Atlantic ocean temperature. First-year sea ice reached its maximum at 12.4–11.8 ka during the Younger Dryas, after which openwater conditions started to dominate, consistent with sea ice records from the eastern Nordic Seas and the North Icelandic shelf. Our results show that over the last 120 000 years, multiyear sea ice extent was greatest during Marine Isotope Stage (MIS) 2 and possibly during MIS 4, with more extended firstyear sea ice during MIS 3 and MIS 5. Sea ice extent during the Holocene (MIS 1) has been less than at any time in the last 120 000 years.

Correction to: Organic phosphorus in the terrestrial environment: a perspective on the state of the art and future priorities

The article “Organic phosphorus in the terrestrial environment: a perspective on the state of the art and future priorities”, written by Timothy S George et al., was originally published with incorrect affiliation information for one of the co-authors, E. Klumpp.