ORCID Profile
0000-0001-8635-9193
Current Organisations
Universita Ca Foscari Dipartimento di Scienze Ambientali
,
Istituto di Scienze Polari Consiglio Nazionale delle Ricerche
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Sensory Processes, Perception and Performance | Psychology
Publisher: Copernicus GmbH
Date: 08-03-2013
Abstract: Abstract. Sea ice is an important parameter in the climate system and its changes impact upon the polar albedo and the atmospheric and oceanic circulation. Iodine (I) and bromine (Br) have been measured in a shallow ice core drilled at the summit of the Holtedahlfonna glacier (Northwest Spitsbergen, Svalbard). Changing I concentrations can be linked to the spring maximum sea ice extension. Bromine enrichment, indexed to the Br/Na sea water mass ratio, appears to be influenced by changes in the seasonal sea ice area. I is emitted from marine biota and so the retreat of spring sea ice coincides with enlargement of the open ocean surface which enhances marine primary production and consequent I emission. The observed Br enrichment can be explained by greater Br emissions during the Br explosion that have been observed to occur above first year sea ice during the early springtime. In this work we present the first comparison between halogens in surface snow and Arctic sea ice extension. Although further investigation is required to characterize potential depositional and post-depositional processes, these preliminary findings suggest that I and Br can be linked to variability in the spring maximum sea ice extension and seasonal sea ice surface area.
Publisher: Royal Society of Chemistry (RSC)
Date: 2012
DOI: 10.1039/C1JA10276A
Publisher: Copernicus GmbH
Date: 24-08-2015
Abstract: Abstract. The role of sea ice in the Earth climate system is still under debate, although it is known to influence albedo, ocean circulation, and atmosphere-ocean heat and gas exchange. Here we present a reconstruction of AD 1950 to 1998 sea ice in the Laptev Sea based on the Akademii Nauk ice core (Severnaya Zemlya, Russian Arctic). The halogens bromine (Br) and iodine (I) are strongly influenced by sea ice processes. Bromine reacts with the sea ice surface in auto-catalyzing "Bromine explosion" events causing an enrichment of the Br / Na ratio and the bromine excess (Brexc) in snow compared to that in seawater. Iodine is emitted from algal communities growing under sea ice. The results suggest a connection between Brexc and spring sea ice area, as well as a connection between iodine concentration and summer sea ice area. These two halogens are therefore good candidates for extended reconstructions of past sea ice changes in the Arctic.
Publisher: Springer Science and Business Media LLC
Date: 30-06-2015
DOI: 10.1007/S00216-015-8820-1
Abstract: A simple and accurate methodology for Br isotope ratio measurements in seawater by multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS) with pneumatic nebulization for s le introduction was developed. The Br(+) signals could be measured interference-free at high mass resolution. Memory effects for Br were counteracted using 5 mmol L(-1) of NH4OH in s le, standard, and wash solutions. The major cation load of seawater was removed via cation exchange chromatography using Dowex 50WX8 resin. Subsequent Br preconcentration was accomplished via evaporation of the s le solution at 90 °C, which did not induce Br losses or isotope fractionation. Mass discrimination was corrected for by external correction using a Cl-matched standard measured in a s le-standard bracketing approach, although Sr, Ge, and Se were also tested as potential internal standards for internal correction for mass discrimination. The δ(81)Br (versus standard mean ocean bromide (SMOB)) values thus obtained for the NaBr isotopic reference material NIST SRM 977 and for IRMM BCR-403 seawater certified reference material are in agreement with literature values. For NIST SRM 977, the (81)Br/(79)Br ratio (0.97291) was determined with a precision ≤0.08‰ relative standard deviation (RSD).
Publisher: Copernicus GmbH
Date: 31-10-2013
Abstract: Abstract. Sea ice is an important parameter in the climate system and its changes impact upon the polar albedo and atmospheric and oceanic circulation. Iodine (I) and bromine (Br) have been measured in a shallow firn core drilled at the summit of the Holtedahlfonna glacier (Northwest Spitsbergen, Svalbard). Changing I concentrations can be linked to the March–May maximum sea ice extension. Bromine enrichment, indexed to the Br / Na sea water mass ratio, appears to be influenced by changes in the seasonal sea ice area. I is emitted from marine biota and so the retreat of March–May sea ice coincides with enlargement of the open-ocean surface which enhances marine primary production and consequent I emission. The observed Br enrichment could be explained by greater Br emissions during the Br explosions that have been observed to occur mainly above first year sea ice during the early springtime. In this work we present the first comparison between halogens in surface snow and Arctic sea ice extension. Although further investigation is required to characterize potential depositional and post-depositional processes, these preliminary findings suggest that I and Br can be linked to variability in the spring maximum sea ice extension and seasonal sea ice surface area.
Publisher: Copernicus GmbH
Date: 05-12-2012
Abstract: Abstract. Atmospheric fluxes of iron (Fe) over the past 200 kyr are reported for the coastal Antarctic Talos Dome ice core, based on acid leachable Fe concentrations. Fluxes of Fe to Talos Dome were consistently greater than those at Dome C, with the greatest difference observed during interglacial climates. We observe different Fe flux trends at Dome C and Talos Dome during the deglaciation and early Holocene, attributed to a combination of deglacial activation of dust sources local to Talos Dome and reorganization of atmospheric transport pathways with the retreat of the Ross Sea ice shelf. This supports similar findings based on dust particle sizes and fluxes and Rare Earth Element fluxes. We show that Ca and Fe should not be used as quantitative proxies for mineral dust, as they all demonstrate different deglacial trends at Talos Dome and Dome C. Considering that a 20 ppmv decrease in atmospheric CO2 at the coldest part of the last glacial maximum occurs contemporaneously with the period of greatest Fe and dust flux to Antarctica, we conclude that the maximum contribution of aeolian dust deposition to Southern Ocean sequestration of atmospheric CO2 is approximately 20 ppmv.
Publisher: Copernicus GmbH
Date: 12-07-2013
Abstract: Abstract. Sea ice is an integral part of the earth's climate system because it affects planetary albedo, sea-surface salinity, and the atmosphere–ocean exchange of reactive gases and aerosols. Bromine and iodine chemistry is active at polar sea ice margins with the occurrence of bromine explosions and the biological production of organoiodine from sea ice algae. Satellite measurements demonstrate that concentrations of bromine oxide (BrO) and iodine oxide (IO) decrease over sea ice toward the Antarctic interior. Here we present speciation measurements of bromine and iodine in the TALDICE (TALos Dome Ice CorE) ice core (159°11' E, 72°49' S 2315 m a.s.l.) spanning the last 215 ky. The Talos Dome ice core is located 250 km inland and is sensitive to marine air masses intruding onto the Antarctic Plateau. Talos Dome bromide (Br−) is positively correlated with temperature and negatively correlated with sodium (Na). Based on the Br−/Na seawater ratio, bromide is depleted in the ice during glacial periods and enriched during interglacial periods. Total iodine, consisting of iodide (I−) and iodate (IO3−), peaks during glacials with lower values during interglacial periods. Although IO3− is considered the most stable iodine species in the atmosphere it was only observed in the TALDICE record during glacial maxima. Sea ice dynamics are arguably the primary driver of halogen fluxes over glacial–interglacial timescales, by altering the distance between the sea ice edge and the Antarctic plateau and by altering the surface area of sea ice available to algal colonization. Based on our results we propose the use of both halogens for examining Antarctic variability of past sea ice extent.
Publisher: Copernicus GmbH
Date: 13-07-2016
DOI: 10.5194/CP-2016-74
Abstract: Abstract. The Law Dome site is ideal for the evaluation of sea ice proxies due to its location near to the Antarctic coast, regular and high accumulation throughout the year, an absence of surface melting or remobilization, and minimal multiyear sea ice. We present records of bromine and iodine concentrations and their enrichment beyond seawater compositions, arguing that halogen enrichment is indicative of the local sea ice area, particularly the 90–110° E sector of the Wilkes coast. Our findings support the results of previous studies of sea ice variability from Law Dome, indicating that Wilkes coast sea ice area is currently at its lowest level since the start of the 20th century. From the Law Dome DSS1213 firn core, 26 years of monthly deposition data indicate that the period of peak bromine enrichment is during Austral spring-summer, from November to February. Results from a traverse along the lee (Western) side of Law Dome show low levels of sodium and bromine deposition, with the greatest fluxes in the vicinity of the Law Dome summit. Finally, iodine enrichment is well correlated to that of bromine, indicating a common, sea ice source for their enrichment.
Publisher: Springer Science and Business Media LLC
Date: 21-09-2016
DOI: 10.1038/SREP33925
Abstract: Reconstructing the past variability of Arctic sea ice provides an essential context for recent multi-year sea ice decline, although few quantitative reconstructions cover the Holocene period prior to the earliest historical records 1,200 years ago. Photochemical recycling of bromine is observed over first-year, or seasonal, sea ice in so-called “bromine explosions” and we employ a 1-D chemistry transport model to quantify processes of bromine enrichment over first-year sea ice and depositional transport over multi-year sea ice and land ice. We report bromine enrichment in the Northwest Greenland Eemian NEEM ice core since the end of the Eemian interglacial 120,000 years ago, finding the maximum extension of first-year sea ice occurred approximately 9,000 years ago during the Holocene climate optimum, when Greenland temperatures were 2 to 3 °C above present values. First-year sea ice extent was lowest during the glacial stadials suggesting complete coverage of the Arctic Ocean by multi-year sea ice. These findings demonstrate a clear relationship between temperature and first-year sea ice extent in the Arctic and suggest multi-year sea ice will continue to decline as polar lification drives Arctic temperatures beyond the 2 °C global average warming target of the recent COP21 Paris climate agreement.
Publisher: Copernicus GmbH
Date: 18-12-2019
Abstract: Abstract. Atmospheric iodine chemistry has a large influence on the oxidizing capacity and associated radiative impacts in the troposphere. However, information on the evolution of past atmospheric iodine levels is restricted to the industrial period while its long-term natural variability remains unknown. The current levels of iodine in the atmosphere are controlled by anthropogenic ozone deposition to the ocean surface. Here, using high-resolution geochemical measurements from coastal eastern Greenland ReCAP (REnland ice CAP project) ice core, we report the first record of atmospheric iodine variability in the North Atlantic during the Holocene (i.e., the last 11 700 years). Surprisingly, our results reveal that the highest iodine concentrations in the record were found during the Holocene Thermal Maximum (HTM ∼ 11 500–5500 years before-present). These high iodine levels could be driven by marine primary productivity resulting in an Early Holocene “biological iodine explosion”. The high and stable iodine levels during this past warm period are a useful observational constraint on projections of future changes in Arctic atmospheric composition and climate resulting from global warming.
Publisher: Copernicus GmbH
Date: 23-02-2021
Abstract: Abstract. Iron (Fe) is a key element in the Earth climate system, as it can enhance marine primary productivity in the high-nutrient low-chlorophyll (HNLC) regions where, despite a high concentration of major nutrients, chlorophyll production is low due to iron limitation. Eolian mineral dust represents one of the main Fe sources to the oceans thus, quantifying its variability over the last glacial cycle is crucial to evaluate its role in strengthening the biological carbon pump. Polar ice cores, which preserve detailed climate records in their stratigraphy, provide a sensitive and continuous archive for reconstructing past eolian Fe fluxes. Here, we show the Northern Hemisphere Fe record retrieved from the NEEM ice core (Greenland), which offers a unique opportunity to reconstruct the past Fe fluxes in a portion of the Arctic over the last 108 kyr. Holocene Fe fluxes (0.042–11.7 ka, 0.5 mg m−2 yr−1) at the NEEM site were 4 times lower than the average recorded over the last glacial period (11.7–108 ka, 2.0 mg m−2 yr−1), whereas they were greater during the Last Glacial Maximum (LGM 14.5–26.5 ka, 3.6 mg m−2 yr−1) and Marine Isotope Stage 4 (MIS 4 60–71 ka, 5.8 mg m−2 yr−1). Comparing the NEEM Fe record with paleoceanographic records retrieved from the HNLC North Pacific, we found that the coldest periods, characterized by the highest Fe fluxes, were distinguished by low marine primary productivity in the subarctic Pacific Ocean, likely due to the greater sea ice extent and the absence of major nutrients upwelling. This supports the hypothesis that Fe fertilization during colder and dustier periods (i.e., LGM and MIS 4) was more effective in other regions, such as the midlatitude North Pacific, where a closer relationship between marine productivity and the NEEM Fe fluxes was observed.
Publisher: Copernicus GmbH
Date: 08-03-2013
Abstract: Abstract. Atmospheric fluxes of iron (Fe) over the past 200 kyr are reported for the coastal Antarctic Talos Dome ice core, based on acid leachable Fe concentrations. Fluxes of Fe to Talos Dome were consistently greater than those at Dome C, with the greatest difference observed during interglacial climates. We observe different Fe flux trends at Dome C and Talos Dome during the deglaciation and early Holocene, attributed to a combination of deglacial activation of dust sources local to Talos Dome and the reorganisation of atmospheric transport pathways with the retreat of the Ross Sea ice shelf. This supports similar findings based on dust particle sizes and fluxes and Rare Earth Element fluxes. We show that Ca and Fe should not be used as quantitative proxies for mineral dust, as they all demonstrate different deglacial trends at Talos Dome and Dome C. Considering that a 20 ppmv decrease in atmospheric CO2 at the coldest part of the last glacial maximum occurs contemporaneously with the period of greatest Fe and dust flux to Antarctica, we confirm that the maximum contribution of aeolian dust deposition to Southern Ocean sequestration of atmospheric CO2 is approximately 20 ppmv.
Publisher: Copernicus GmbH
Date: 28-02-2014
Publisher: Copernicus GmbH
Date: 25-07-2023
DOI: 10.5194/CP-2023-52
Abstract: Abstract. Climate reconstructions of the last millennium rely on networks of high resolution and well-dated proxy records. This study presents age-at-depth data and preliminary results from the new Mount Brown South ice cores, collected at an elevation of 2,084 metres on the boundary of Princess Elizabeth and Kaiser Wilhelm II Land in East Antarctica. We show an initial analysis of the site meteorology, mean annual chemical species concentrations, and seasonal cycles including analysis of a seasonal cycle in fluoride concentrations with a potential link to sea ice formation. The annually resolved chronologies were developed from this data using a site-specific layer-counting methodology which employed seasonally varying trace chemical species and water isotope ratios, combined with a volcanic horizon alignment approach. The chronologies developed include the ‘Main’ 295 m record spanning 1,137 years (873–2009 CE), and three surface cores spanning the most recent 39–52 years up to the surface age at the time of drilling (austral summer 2017/2018). Mean annual trace chemical concentrations are compared to the Law Dome ice core further to the east and discussed in terms of atmospheric transport, and the uncertainty in the determination of annual horizons via layer counting is quantified. The MBS chronologies presented here – named MBS2023 – will underpin the development of new palaeoclimate records spanning the past millennium from this under-represented region of East Antarctica.
Publisher: American Geophysical Union (AGU)
Date: 27-04-2013
DOI: 10.1002/GRL.50296
Publisher: Springer Science and Business Media LLC
Date: 17-02-2012
DOI: 10.1007/S00216-012-5806-0
Abstract: Iodine and bromine species participate in key atmospheric reactions including the formation of cloud condensation nuclei and ozone depletion. We present a novel method coupling a high-performance liquid chromatography with ion chromatography and inductively coupled plasma mass spectrometry, which allows the determination of iodine (I) and bromine (Br) species (IO(3)(-), I(-), Br(-), BrO(3)(-) ) at the picogram-per-gram levels presents in Antarctic ice. Chromatographic separation was achieved using an IONPAC® AS16 Analytical Column with NaOH as eluent. Detection limits for I and Br species were 5 to 9 pg g(-1) with an uncertainty of less than 2.5% for all considered species. Inorganic iodine and bromine species have been determined in Antarctic ice core s les, with concentrations close to the detection limits for iodine species, and approximately 150 pg g(-1) for Br(-). Although iodate (IO(3)(-)) is the most abundant iodine species in the atmosphere, only the much rarer iodide (I(-)) species was present in Antarctic Holocene ice. Bromine was found to be present in Antarctic ice as Br(-).
Publisher: Copernicus GmbH
Date: 17-10-2016
DOI: 10.5194/TC-2016-220
Abstract: Abstract. Halogen chemistry in the polar regions occurs through the release of sea salt rich aerosols from sea ice surfaces and organic compounds from algae colonies living within the sea ice environment. Measurements of halogen species in polar snow s les are limited to a few sites although they are shown to be closely related to sea ice extent. We examine here total bromine, iodine and sodium concentrations in a series of 2 m cores collected during a traverse from Talos Dome (72°48' S, 159°06' E) to GV7 (70°41' S, 158°51' E), analyzed by Inductively Coupled Plasma Sector Field Mass Spectrometry (ICP-SFMS) at a resolution of 5 cm. We find a distinct seasonality of the bromine enrichment signal in all cores, with maxima during the austral late spring. Iodine showed average concentrations of 0.04 ppb with little variability. No distinct seasonality was found for iodine and sodium. The transect revealed homogeneous fluxes for the three chemical species along the transect, due to competing effects of air masses originating from the Ross Sea and the Southern Ocean. The flux measurements are consistent with the uniform values of BrO and IO detected from satellite observations. Similar trends are found for annual bromine enrichment and 130–190° E First Year Sea Ice for the 2010–2013 period.
Publisher: Copernicus GmbH
Date: 16-09-2014
Abstract: Abstract. The atmospheric chemistry of iodine and bromine in Polar regions is of interest due to the key role of halogens in many atmospheric processes, particularly tropospheric ozone destruction. Bromine is emitted from the open ocean but is enriched above first-year sea ice during springtime bromine explosion events, whereas iodine emission is attributed to biological communities in the open ocean and hosted by sea ice. It has been previously demonstrated that bromine and iodine are present in Antarctic ice over glacial–interglacial cycles. Here we investigate seasonal variability of bromine and iodine in polar snow and ice, to evaluate their emission, transport and deposition in Antarctica and the Arctic and better understand potential links to sea ice. We find that bromine and iodine concentrations and Br enrichment (relative to sea salt content) in polar ice do vary seasonally in Arctic snow and Antarctic ice. Although seasonal variability in halogen emission sources is recorded by satellite-based observations of tropospheric halogen concentrations, seasonal patterns observed in snowpack are likely also influenced by photolysis-driven processes. Peaks of bromine concentration and Br enrichment in Arctic snow and Antarctic ice occur in spring and summer, when sunlight is present. A secondary bromine peak, observed at the end of summer, is attributed to bromine deposition at the end of the polar day. Iodine concentrations are largest in winter Antarctic ice strata, contrary to contemporary observations of summer maxima in iodine emissions. These findings support previous observations of iodine peaks in winter snow strata attributed to the absence of sunlight-driven photolytic re-mobilisation of iodine from surface snow. Further investigation is required to confirm these proposed mechanisms explaining observations of halogens in polar snow and ice, and to evaluate the extent to which halogens may be applied as sea ice proxies.
Publisher: Copernicus GmbH
Date: 28-02-2014
Abstract: Abstract. Biomass burning is a major source of greenhouse gases and influences regional to global climate. Pre-industrial fire-history records from black carbon, charcoal and other proxies provide baseline estimates of biomass burning at local to global scales, but there remains a need for broad-scale fire proxies that span millennia in order to understand the role of fire in the carbon cycle and climate system. We use the specific biomarker levoglucosan, and multi-source black carbon and ammonium concentrations to reconstruct fire activity from the North Greenland Eemian (NEEM) ice cores (77.49° N 51.2° W, 2480 m a.s.l.) over the past 2000 years. Increases in boreal fire activity (1000–1300 CE and 1500–1700 CE) over multi-decadal timescales coincide with the most extensive central and northern Asian droughts of the past two millennia. The NEEM biomass burning tracers coincide with temperature changes throughout much of the past 2000 years except for during the extreme droughts, when precipitation changes are the dominant factor. Many of these multi-annual droughts are caused by monsoon failures, thus suggesting a connection between low and high latitude climate processes. North America is a primary source of biomass burning aerosols due to its relative proximity to the NEEM c . During major fire events, however, isotopic analyses of dust, back-trajectories and links with levoglucosan peaks and regional drought reconstructions suggest that Siberia is also an important source of pyrogenic aerosols to Greenland.
Publisher: Copernicus GmbH
Date: 22-03-2021
Publisher: Copernicus GmbH
Date: 07-02-2023
Abstract: Abstract. Insoluble particles in ice cores record signatures of past climate parameters like vegetation dynamics, volcanic activity, and aridity. For some of them, the analytical detection relies on intensive bench microscopy investigation and requires dedicated s le preparation steps. Both are laborious, require in-depth knowledge, and often restrict s ling strategies. To help overcome these limitations, we present a framework based on flow imaging microscopy coupled to a deep neural network for autonomous image classification of ice core particles. We train the network to classify seven commonly found classes, namely mineral dust, felsic and mafic (basaltic) volcanic ash grains (tephra), three species of pollen (Corylus avellana, Quercus robur, Quercus suber), and contamination particles that may be introduced onto the ice core surface during core handling operations. The trained network achieves 96.8 % classification accuracy at test time. We present the system's potential and its limitations with respect to the detection of mineral dust, pollen grains, and tephra shards, using both controlled materials and real ice core s les. The methodology requires little s le material, is non-destructive, fully reproducible, and does not require any s le preparation procedures. The presented framework can bolster research in the field by cutting down processing time, supporting human-operated microscopy, and further unlocking the paleoclimate potential of ice core records by providing the opportunity to identify an array of ice core particles. Suggestions for an improved system to be deployed within a continuous flow analysis workflow are also presented.
Publisher: Proceedings of the National Academy of Sciences
Date: 24-10-2022
Abstract: 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 (Br enr ) 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 litude of high-frequency sea ice fluctuations increased through interstadials. Our findings suggest that the rapid replacement of widespread MYSI with seasonal sea ice lified 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.
Publisher: Copernicus GmbH
Date: 20-07-2021
Abstract: Abstract. 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 millennium human activities might have influenced wildfire frequency/occurrence substantially.
Publisher: Copernicus GmbH
Date: 19-12-2019
Abstract: Abstract. 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 open-water 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, multi-year sea ice extent was greatest during Marine Isotope Stage (MIS) 2 and possibly during MIS 4, with more extended first-year 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.
Publisher: Copernicus GmbH
Date: 13-06-2019
Publisher: Copernicus GmbH
Date: 23-03-2020
DOI: 10.5194/EGUSPHERE-EGU2020-3520
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Publisher: Copernicus GmbH
Date: 29-10-2014
Abstract: Abstract. Biomass burning is a major source of greenhouse gases and influences regional to global climate. Pre-industrial fire-history records from black carbon, charcoal and other proxies provide baseline estimates of biomass burning at local to global scales spanning millennia, and are thus useful to examine the role of fire in the carbon cycle and climate system. Here we use the specific biomarker levoglucosan together with black carbon and ammonium concentrations from the North Greenland Eemian (NEEM) ice cores (77.49° N, 51.2° W 2480 m a.s.l) over the past 2000 years to infer changes in boreal fire activity. Increases in boreal fire activity over the periods 1000–1300 CE and decreases during 700–900 CE coincide with high-latitude NH temperature changes. Levoglucosan concentrations in the NEEM ice cores peak between 1500 and 1700 CE, and most levoglucosan spikes coincide with the most extensive central and northern Asian droughts of the past millennium. Many of these multi-annual droughts are caused by Asian monsoon failures, thus suggesting a connection between low- and high-latitude climate processes. North America is a primary source of biomass burning aerosols due to its relative proximity to the Greenland Ice Cap. During major fire events, however, isotopic analyses of dust, back trajectories and links with levoglucosan peaks and regional drought reconstructions suggest that Siberia is also an important source of pyrogenic aerosols to Greenland.
Publisher: Copernicus GmbH
Date: 21-12-2017
DOI: 10.5194/CP-2017-158
Abstract: Abstract. Abstract. High latitude Southern Hemisphere fire history was reconstructed by determining the specific biomarker levoglucosan in ice cores from the TALos Dome Ice CorE drilling project (TALDICE) during the Mid-Late Holocene (750–6000 yr BP). Potassium was also analyzed in order to provide a comparison with another fire proxy to create a more robust biomass burning record. The levoglucosan record is characterized by a long-term increase with higher rates starting at ~ 4000 yr BP and higher peaks between 1500 and 2500 yr BP. Comparisons with charcoal syntheses help evaluate fire sources, showing a possible higher contribution from Patagonian fires rather than Australian biomass burning. We interpret the anomalous increase in levoglucosan centred at ~ 2000 yr BP as a combination of the atmospheric transport pathway and the interplay between climatic factors.
Publisher: Copernicus GmbH
Date: 12-02-2013
DOI: 10.5194/ACPD-13-3881-2013
Abstract: Abstract. Sea ice is an integral part of the Earth's climate system because it affects planetary albedo, sea surface salinity, and the atmosphere-ocean exchange of reactive gases and aerosols. Bromine and iodine chemistry is active at polar sea ice margins with the occurrence of bromine explosions and the biological production of organo-iodine from sea ice algae. Satellite measurements demonstrate that concentrations of bromine oxide (BrO) and iodine oxide (IO) decrease over sea ice toward the Antarctic interior. Here we present speciation measurements of bromine and iodine in the TALDICE (TALos Dome Ice CorE) ice core (159°11' E, 72°49' S, 2315 m a.s.l.) spanning the last 215 ky. The Talos Dome ice core is located 250 km inland and is sensitive to marine air masses intruding onto the Antarctic Plateau. Talos Dome bromide (Br−) is positively correlated with temperature and negatively correlated with sodium (Na). Based on the Br−/Na seawater ratio, bromide is depleted in the ice during glacial periods and enriched during interglacial periods. Total iodine, consisting of iodide (I−) and iodate (IO3−), peaks during glacials with lower values during interglacial periods. Although IO3− is considered the most stable iodine species in the atmosphere it was only observed in the TALDICE record during glacial maxima. Sea ice dynamics are arguably the primary driver of halogen fluxes over glacial-interglacial timescales, by altering the distance between the sea ice edge and the Antarctic plateau and by altering the surface area of sea ice available to algal colonization. Based on our results we propose the use of both halogens for examining Antarctic variability of past sea ice extent.
Publisher: Elsevier BV
Date: 12-2021
Publisher: Copernicus GmbH
Date: 27-02-2017
Abstract: Abstract. The Law Dome site is ideal for the evaluation of sea ice proxies due to its location near to the Antarctic coast, regular and high accumulation throughout the year, an absence of surface melting or remobilization, and minimal multiyear sea ice. We present records of bromine and iodine concentrations and their enrichment beyond seawater compositions and compare these to satellite observations of first-year sea ice area in the 90–130° E sector of the Wilkes coast. Our findings support the results of previous studies of sea ice variability from Law Dome, indicating that Wilkes coast sea ice area is currently at its lowest level since the start of the 20th century. From the Law Dome DSS1213 firn core, 26 years of monthly deposition data indicate that the period of peak bromine enrichment is during austral spring–summer, from November to February. Results from a traverse along the lee (western) side of Law Dome show low levels of sodium and bromine deposition, with the greatest fluxes in the vicinity of the Law Dome summit. Finally, multidecadal variability in iodine enrichment appears well correlated to bromine enrichment, suggesting a common source of variability that may be related to the Interdecadal Pacific Oscillation (IPO).
Publisher: Copernicus GmbH
Date: 25-03-2014
DOI: 10.5194/ACPD-14-8185-2014
Abstract: Abstract. The atmospheric chemistry of iodine and bromine in polar regions is of interest due to the key role of halogens in many atmospheric processes, particularly tropospheric ozone destruction. Bromine is emitted from the open ocean but is enriched above first-year sea ice during springtime bromine explosion events, whereas iodine is emitted from biological communities hosted by sea ice. It has been previously demonstrated that bromine and iodine are present in Antarctic ice over glacial-interglacial cycles. Here we investigate seasonal variability of bromine and iodine in polar snow and ice, to evaluate their emission, transport and deposition in Antarctica and the Arctic and better understand potential links to sea ice. We find that bromine enrichment (relative to sea salt content) and iodine concentrations in polar ice do vary seasonally in Arctic snow and Antarctic ice and we relate such variability to satellite-based observations of tropospheric halogen concentrations. Peaks of bromine enrichment in Arctic snow and Antarctic ice occur in spring and summer, when sunlight is present. Iodine concentrations are largest in winter Antarctic ice strata, contrary to contemporary observations of summer maxima in iodine emissions.
Publisher: Copernicus GmbH
Date: 27-03-2020
Abstract: Abstract. Acquiring not only field-specific knowledge but also a set of transferable professional skills becomes increasingly important for Early Career Scientists (ECS) in Geosciences and other academic disciplines. Although the need for training in transferable skills adds to the work-load of an in idual Early Career Scientist, it is often neglected within the traditional academic environments. International Early Career Networks (ECN) are global voluntary communities of early career scientists aiming (i) to advocate for early stage researchers and (ii) to advance the careers of their members by raising their profiles and training them in specific transferable skills, such as networking, collaborating and outreach. Accordingly, ECN can be a tool to move beyond institutional barriers and to improve the inclusion of ECS into the international scientific community. In 2019 we conducted three surveys in order to assess ECN from the perspective of its members and regarding the structures of different ECN within a specific discipline and across disciplines. We use the survey results alongside with case studies from well-established and long term networks to elucidate the attributes that make a successful, sustainable ECN. Important characteristics of these international ECN include (1) developing the ECN organizational schemes to promote early career scientists within a specific discipline and across disciplines, (2) scoping for members needs, evaluating the performance of the network, and adapting to feedback, (3) continuity of the organizing committee by ensuring representation of different stages of ECS, and (4) erse membership to provide strong foundational and personnel support within the network. These characteristics can support the development of best practices for developing ECN successfully, which can guide existing and future networks within Geosciences and other scientific disciplines.
Publisher: Copernicus GmbH
Date: 27-03-2022
DOI: 10.5194/EGUSPHERE-EGU22-5683
Abstract: & & Over the last four decades, the Southern Ocean has been characterized by now-persistent stronger westerly winds, with consequences for the Antarctic region climate, including variations in sea ice extent and primary productivity. Here we present the first ever bromine, sodium and iodine records, tracers of sea salt aerosols, sea ice and primary productivity, from five sub-Antarctic ice cores, retrieved from Bouvet, Young, Peter I and Mount Siple Island and Mertz glacier. The aim of the study is (1) to assess if halogens deposited in sub-Antarctic regions are influenced by recent changes in wind forcing and (2) to better understand the underlying processes of halogens emission from ocean/sea ice, their transport and deposition over the Antarctic region.& & & & The trends of sodium and bromine, emitted and transported with sea salt aerosols, suggest that wind strengthening leads to more halogens deposited in the sub-Antarctic. Also, we find that bromine is depleted with respect to the bromine-to-sodium sea-water ratio at all sites, indicating that bromine species are sustained in the marine boundary layer by halogen chemistry and are less prone to be deposited. Iodine records show a positive correlation with marginal sea ice and primary productivity variability, suggesting that iodine species emitted at the edge are deposited more efficiently than bromine species.& &
Publisher: Copernicus GmbH
Date: 24-08-2015
Publisher: Copernicus GmbH
Date: 17-07-2018
DOI: 10.5194/CP-2018-80
Abstract: Abstract. Although it has been demonstrated that the speed and magnitude of recent Arctic sea ice decline is unprecedented for the past 1,450 years, few records are available to provide a paleoclimate context for Arctic sea ice extent. Here we present a 120 kyr record of bromine enrichment from the RECAP ice core, coastal East Greenland, and reconstruct past sea ice conditions in the North Atlantic as far north as the entrance of the Arctic Ocean (50–85° N). Bromine enrichment has been previously employed to reconstruct first-year sea ice (FYSI) in the Canadian Arctic over the last glacial cycle. We find that during the last deglaciation, the transition from multi-year sea ice (MYSI) to FYSI started at ∼ 17.6 kyr, synchronous with sea ice reductions observed in the eastern Nordic seas (Müller and Stein, 2014 Hoff et al., 2016) and with the increase of North Atlantic ocean temperature (Dokken and Jansen, 1999). FYSI reached its maximum extent at 12.4–11.8 kyr, after which open-water conditions started to dominate, as supported by sea ice records from the eastern Nordic seas and the North Icelandic shelf. Our results show that over the last 120,000 years, sea ice extent was greatest during Marine Isotope Stage (MIS) 2 and MIS4, with decreased levels during MIS3 and the onset of the last glacial period (late-MIS5). Sea ice extent during the last 10 kyr (Holocene/MIS1) has been less than at any time in the last 120 kyr.
Publisher: Copernicus GmbH
Date: 13-06-2019
DOI: 10.5194/CP-2019-71
Abstract: Abstract. Atmospheric iodine chemistry has a large influence on oxidizing capacity and associated radiative impacts in the troposphere. However, information on the evolution of atmospheric iodine levels is restricted to the Industrial Period while its long-term natural variability remains unknown. The current levels of iodine in the atmosphere are controlled by anthropogenic ozone deposition to the ocean surface. Here, using high-resolution ice core measurements from coastal eastern Greenland (ReCAP ice core), we report the first record of atmospheric iodine variability during the Holocene (last 11,700 years). Surprisingly, our results reveal that the highest iodine concentrations in the record, found during the Holocene Thermal Maximum (~ 11,500-–5,500 years before -present). These high iodine levels could be driven by ocean primary productivity resulting in an Early Holocene “Biological Iodine Explosion”. The iodine trend during this past warm period is a useful observational constraint on projections of future changes in Arctic atmospheric composition and climate resulting from global warming.
Publisher: Copernicus GmbH
Date: 21-06-2018
Abstract: Abstract. We determined the specific biomass burning biomarker levoglucosan in an ice core from the TALos Dome Ice CorE drilling project (TALDICE) during the mid- to late Holocene (6000–750 BP). The levoglucosan record is characterized by a long-term increase with higher rates starting at ∼ 4000 BP and peaks between 2500 and 1500 BP. The anomalous increase in levoglucosan centered at ∼ 2000 BP is consistent with other Antarctic biomass burning records. Multiple atmospheric phenomena affect the coastal Antarctic Talos Dome drilling site, where the Southern Annular Mode (SAM) is the most prominent as the Southern Annular Mode Index (SAMA) correlates with stable isotopes in precipitation throughout the most recent 1000 years of the ice core. If this connection remains throughout the mid- to late Holocene, then our results demonstrate that changes in biomass burning, rather than changes in atmospheric transport, are the major influence on the TALDICE levoglucosan record. Comparisons with charcoal syntheses help evaluate fire sources, showing a greater contribution from southern South American fires than from Australian biomass burning. The levoglucosan peak centered at ∼ 2000 BP occurs during a cool period throughout the Southern Hemisphere, yet during a time of increased fire activity in both northern and southern Patagonia. This peak in biomass burning is influenced by increased vegetation in southern South America from a preceding humid period, in which the vegetation desiccated during the following cool, dry period. The Talos Dome ice core record from 6000 to ∼ 750 BP currently does not provide clear evidence that the fire record may be strongly affected by anthropogenic activities during the mid- to late Holocene, although we cannot exclude at least a partial influence.
Publisher: Copernicus GmbH
Date: 13-07-2016
Publisher: Springer Science and Business Media LLC
Date: 13-06-2012
DOI: 10.1007/S00216-012-6166-5
Abstract: Iron and aluminium are the two most abundant metals on the Earth's crust, but they display quite different biogeochemical properties. While iron is essential to many biological processes, aluminium has not been found to have any biological function at all. In environmental studies, iron has been studied in detail for its limiting role in the bioproductivity of high nutrient, low carbon oceanic zones, while aluminium is routinely used as a reference of crustal contributions to atmospheric deposition archives including peat bogs, lacustrine and marine sediments and ice sheets and glaciers. We report here the development of a flow injection analysis technique, which has been optimised for the simultaneous determination of soluble iron and aluminium in polar ice cores. Iron was determined by its catalytic role in the reduction of N,N-dimethyl-p-phenylenediamene (DPD) to a semiquinonic form (DPDQ) and subsequent absorption spectroscopy at 514 nm. Aluminium was determined by spectroscopic analysis of an aluminium-lumogallion complex that exhibits fluorescence at 560 nm. These techniques have been applied to a section of Greenland ice dated to 1729-1733 AD and indicate that volcanism is a source of highly soluble aluminium and iron.
Publisher: Copernicus GmbH
Date: 17-03-2017
Abstract: Abstract. Halogen chemistry in the polar regions occurs through the release of halogen elements from different sources. Bromine is primarily emitted from sea salt aerosols and other saline condensed phases associated with sea ice surfaces, while iodine is affected by the release of organic compounds from algae colonies living within the sea ice environment. Measurements of halogen species in polar snow s les are limited to a few sites although there is some evidence that they are related to sea ice extent. We examine here total bromine, iodine and sodium concentrations in a series of 2 m cores collected during a traverse from Talos Dome (72°48' S, 159°06' E) to GV7 (70°41' S, 158°51' E) analyzed by inductively coupled plasma-sector field mass spectrometry (ICP-SFMS) at a resolution of 5 cm. We find a distinct seasonality of the bromine enrichment signal in most of the cores, with maxima during the austral spring. Iodine shows average concentrations of 0.04 ppb with little variability. No distinct seasonality is found for iodine and sodium. The transect reveals homogeneous air-to-snow fluxes for the three chemical species along the transect due to competing effects of air masses originating from the Ross Sea and the Southern Ocean.
Publisher: Proceedings of the National Academy of Sciences
Date: 09-11-2020
Abstract: The last glacial period was marked by abrupt, high- litude Greenland warming events, known as Dansgaard–Oeschger (D-O) events, which were likely linked with Nordic Seas sea ice retreat. We reconstruct the sea ice variability during four D-O events ∼32–41 ka with unprecedented spatial representation and rigorous temporal constraints, using proxy records from two Norwegian Sea sediment cores and an East Greenland ice core. Our records reveal millennial-scale variations between extended sea ice conditions and reduced seasonal sea ice conditions, with rapid sea ice reductions at the onset of D-O events. Our findings imply that rapid sea ice reduction lified ocean-atmosphere processes causing the abrupt D-O climate transitions, providing constraints for model simulations of abrupt climate changes and their mechanisms.
Publisher: Copernicus GmbH
Date: 10-07-2020
DOI: 10.5194/CP-2020-77
Abstract: Abstract. Iron is a key element in the Earth climate system as it can enhance the marine primary productivity in the High-Nutrient Low-Chlorophyll (HNLC) regions where, despite a high concentration of major nutrients, the chlorophyll production is low due to iron limitation. One of the main Fe sources to the ocean is Aeolian dust. For this reason, ice cores provide a sensitive and continuous archive for reconstructing Fe fluxes over the last millennia. Here we show the first Northern Hemisphere Fe record retrieved from the NEEM ice core, which offers a unique opportunity to reconstruct the past Fe fluxes in the Arctic region over the last 108 kyr. Holocene Fe fluxes to the Arctic were three times lower than the average recorded over the last glacial period. They were greater during the Last Glacial Maximum (LGM) and the Marine Isotope Stage 4 (MIS 4). Comparing our data with palaeoceanographic records retrieved from the HNLC North Pacific, we demonstrated that during the coldest periods, characterized by the highest Fe fluxes, marine productivity in the subarctic Pacific Ocean did not increase due to a greater sea-ice extent and the absence of upwelling nutrient supply. This supports the hypothesis that Fe-fertilization was more effective in other regions, such as the transition zone of the North Pacific, where a closer relationship between marine productivity and the Aeolian Fe fluxes was observed.
Publisher: Springer Science and Business Media LLC
Date: 16-04-2018
DOI: 10.1038/S41467-018-03924-3
Abstract: 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.
Publisher: Copernicus GmbH
Date: 26-01-2016
Abstract: Abstract. The role of sea ice in the Earth climate system is still under debate, although it is known to influence albedo, ocean circulation, and atmosphere–ocean heat and gas exchange. Here we present a reconstruction of 1950 to 1998 AD sea ice in the Laptev Sea based on the Akademii Nauk ice core (Severnaya Zemlya, Russian Arctic). The chemistry of halogens bromine (Br) and iodine (I) is strongly active and influenced by sea ice dynamics, in terms of physical, chemical and biological process. Bromine reacts on the sea ice surface in autocatalyzing "bromine explosion" events, causing an enrichment of the Br / Na ratio and hence a bromine excess (Brexc) in snow compared to that in seawater. Iodine is suggested to be emitted from algal communities growing under sea ice. The results suggest a connection between Brexc and spring sea ice area, as well as a connection between iodine concentration and summer sea ice area. The correlation coefficients obtained between Brexc and spring sea ice (r = 0.44) as well as between iodine and summer sea ice (r = 0.50) for the Laptev Sea suggest that these two halogens could become good candidates for extended reconstructions of past sea ice changes in the Arctic.
Publisher: Copernicus GmbH
Date: 22-03-2021
DOI: 10.5194/CP-2021-26
Abstract: Abstract. 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 time scales and, in particular, on 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 ice core, drilled in the coastal East Greenland and therefore affected by processes occurring in the High North Atlantic Region. Levoglucosan and ammonium fluxes show high levels from 5 to 4.5 kyr 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 (before 2000 AD), suggesting a decline in wildfire regime in the Icelandic territory due to the extensive land clearing caused by Viking colonizers. A minimum is reached at 0.5 kyr BP for all fire proxies, 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 millennium human activities might have had a substantial influence controlling the occurrence of fire.
Location: Italy
Location: Italy
Start Date: 02-2011
End Date: 03-2015
Amount: $190,000.00
Funder: Australian Research Council
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