Air-ice CO2 fluxes and pCO2 dynamics in the Arctic coastal area (Amundsen Gulf, Canada)

NASA Astrophysics Data System (ADS)

Geilfus, Nicolas-Xavier; Tison, Jean Louis; Carnat, Gauthier; Else, Brent; Borges, Alberto V.; Thomas, Helmuth; Shadwick, Elizabeth; Delille, Bruno

2010-05-01

Sea ice covers about 7% of the Earth surface at its maximum seasonal extent. For decades sea ice was assumed to be an impermeable and inert barrier for air - sea exchange of CO2 so that global climate models do not include CO2 exchange between the oceans and the atmosphere in the polar regions. However, uptake of atmospheric CO2 by sea ice cover was recently reported raising the need to further investigate pCO2 dynamics in the marine cryosphere realm and related air-ice CO2 fluxes. In addition, budget of CO2 fluxes are poorly constrained in high latitudes continental shelves [Borges et al., 2006]. We report measurements of air-ice CO2 fluxes above the Canadian continental shelf and compare them to previous measurements carried out in Antarctica. We carried out measurements of pCO2 within brines and bulk ice, and related air-ice CO2 fluxes (chamber method) in Antarctic first year pack ice ("Sea Ice Mass Balance in Antarctica -SIMBA" drifting station experiment September - October 2007) and in Arctic first year land fast ice ("Circumpolar Flaw Lead" - CFL, April - June 2008). These 2 experiments were carried out in contrasted sites. SIMBA was carried out on sea ice in early spring while CFL was carried out in from the middle of the winter to the late spring while sea ice was melting. Both in Arctic and Antarctic, no air-ice CO2 fluxes were detected when sea ice interface was below -10°C. Slightly above -10°C, fluxes toward the atmosphere were observed. In contrast, at -7°C fluxes from the atmosphere to the ice were significant. The pCO2 of the brine exhibits a same trend in both hemispheres with a strong decrease of the pCO2 anti-correlated with the increase of sea ice temperature. The pCO2 shifted from a large over-saturation at low temperature to a marked under-saturation at high temperature. These air-ice CO2 fluxes are partly controlled by the permeability of the air-ice interface, which depends of the temperature of this one. Moreover, air-ice CO2 fluxes are

Infrared Spectra and Thermodynamic Properties of Co2/Methanol Ices

NASA Astrophysics Data System (ADS)

Maté, Belén; Gálvez, Óscar; Herrero, Víctor J.; Escribano, Rafael

2009-01-01

Ices of mixtures of carbon dioxide and methanol have been studied in a range of temperatures relevant for star-forming regions, comets, polar caps of planets and satellites, and other solar system bodies. We have performed temperature-programmed desorption measurements and recorded IR spectra of various types of samples. The presence of two slightly different structures of CO2 is manifest. A distorted CO2 structure is characterized by bandshifts between 5 cm-1 (ν3) and 10 cm-1 (ν2) with respect to normal CO2. If the samples are heated above 130 K, the distorted CO2 sublimates and only the normal structure remains. The latter can stay trapped until the sublimation of crystalline methanol (150 K). The desorption energy (E d ~ 20 kJ mol-1) of CO2 from methanol ice, and the specific adsorption surface area (6 m2 g-1) of amorphous CH3OH ice, have been determined. CO2 does not penetrate into crystalline ice. Whereas the desorption energy is similar to that of CO2/H2O samples, the specific surface of methanol is much smaller than that of amorphous solid water (ASW). The interaction of CO2 molecules with water and methanol is similar but ices of CH3OH are much less porous than ASW. The inclusion of CO2 into previously formed ices containing these two species would take place preferentially into ASW. However, in processes of simultaneous deposition, methanol ice can admit a larger amount of CO2 than water ice. CO2/CH3OH ices formed by simultaneous deposition admit two orders of magnitude more CO2 than sequentially deposited ices. These findings can have direct relevance to the interpretation of observations from protostellar environments (e.g., RAFGL7009S) and comet nuclei.

An Ice Core Melter System for Continuous Major and Trace Chemical Analyses of a New Mt. Logan Summit Ice Core

NASA Astrophysics Data System (ADS)

Osterberg, E. C.; Handley, M. J.; Sneed, S. D.; Mayewski, P. A.; Kreutz, K. J.; Fisher, D. A.

2004-12-01

The ice core melter system at the University of Maine Climate Change Institute has been recently modified and updated to allow high-resolution (<1-2 cm ice/sample), continuous and coregistered sampling of ice cores, most notably the 2001 Mt. Logan summit ice core (187 m to bedrock), for analyses of 34 trace elements (Sr, Cd, Sb, Cs, Ba, Pb, Bi, U, As, Al, S, Ca, Ti, V, Cr, Mn, Fe, Co, Cu, Zn, REE suite) by inductively coupled plasma mass spectrometry (ICP-MS), 8 major ions (Na+, Ca2+, Mg2+, K+, Cl-, SO42-, NO3-, MSA) by ion chromatography (IC), stable water isotopes (δ 18O, δ D, d) and volcanic tephra. The UMaine continuous melter (UMCoM) system is housed in a dedicated clean room with HEPA filtered air. Standard clean room procedures are employed during melting. A Wagenbach-style continuous melter system has been modified to include a pure Nickel melthead that can be easily dismantled for thorough cleaning. The system allows melting of both ice and firn without wicking of the meltwater into unmelted core. Contrary to ice core melter systems in which the meltwater is directly channeled to online instruments for continuous flow analyses, the UMCoM system collects discrete samples for each chemical analysis under ultraclean conditions. Meltwater from the pristine innermost section of the ice core is split between one fraction collector that accumulates ICP-MS samples in acid pre-cleaned polypropylene vials under a class-100 HEPA clean bench, and a second fraction collector that accumulates IC samples. A third fraction collector accumulates isotope and tephra samples from the potentially contaminated outer portion of the core. This method is advantageous because an archive of each sample remains for subsequent analyses (including trace element isotope ratios), and ICP-MS analytes are scanned for longer intervals and in replicate. Method detection limits, calculated from de-ionized water blanks passed through the entire UMCoM system, are below 10% of average Mt

Ice core carbonyl sulfide measurements from a new South Pole ice core (SPICECORE)

NASA Astrophysics Data System (ADS)

Aydin, M.; Nicewonger, M. R.; Saltzman, E. S.

2017-12-01

Carbonyl sulfide (COS) is the most abundant sulfur gas in the troposphere with a present-day mixing ratio of about 500 ppt. Direct and indirect emissions from the oceans are the predominant sources of atmospheric COS. The primary removal mechanism is uptake by terrestrial plants during photosynthesis. Because plants do not respire COS, atmospheric COS levels are linked to terrestrial gross primary productivity (GPP). Ancient air trapped in polar ice cores has been used to reconstruct COS records of the past atmosphere, which can be used to infer past GPP variability and potential changes in oceanic COS emission. We are currently analyzing samples from a newly drilled intermediate depth ice core from South Pole, Antarctica (SPICECORE). This core is advantageous for studying COS because the cold temperatures of South Pole ice lead to very slow rates of in situ loss due to hydrolysis. One hundred and eighty-four bubbly ice core samples have been analyzed to date with gas ages ranging from about 9.2 thousand (733 m depth) to 75 years (126 m depth) before present. After a 2% correction for gravitational enrichment in the firn, the mean COS mixing ratio for the data set is 312±15 ppt (±1s), with the data set median also equal to 312 ppt. The only significant long-term trend in the record is a 5-10% increase in COS during the last 2-3 thousand years of the Holocene. The SPICECORE data agree with previously published ice core COS records from other Antarctic sites during times of overlap, confirming earlier estimates of COS loss rates to in situ hydrolysis in ice cores. Antarctic ice core data place strict constraints on the COS mixing ratio and its range of variability in the southern hemisphere atmosphere during the last several millennia. Implications for the atmospheric COS budget will be discussed.

First investigations of an ice core from Eisriesenwelt cave (Austria)

NASA Astrophysics Data System (ADS)

May, B.; Spötl, C.; Wagenbach, D.; Dublyansky, Y.; Liebl, J.

2011-02-01

Investigations into the genesis and dynamical properties of cave ice are essential for assessing the climate significance of these underground glaciers. We drilled an ice core through a 7.1 m-thick ice body filling a large cavern of the dynamic ice cave Eisenriesenwelt (Austria). In addition to visual core inspections, quasi-continuous measurements at 2 cm resolution comprised particulate matter, stable water isotope (δ18O, δD) and electrolytic conductivity profiles supplemented by specifically selected samples analyzed for tritium and radiocarbon. We found that recent ablation led to an almost complete loss of bomb-derived tritium removing any ice accumulated since, at least, the early fifties leaving the actual ice surface even below the natural tritium level. The small particulate organic masses rendered radiocarbon dating inconclusive, though a crude estimate gave a basal ice age in the order of several thousand years. The visual stratigraphy and all investigated parameters showed a clear dichotomy between the upper 2 m and the bottom 3 m of the core, which points to a substantial change in the ice formation process. Main features of the core comprise the changing appearance and composition of distinct cryocalcite layers, extremely low total ion content and a surprisingly high variability of the isotope signature. Co-isotope evaluation (δD versus δ18O) of the core in comparison with data from precipitation and karst spring water clearly indicate that ice formation is governed by (slow) freezing of dripping water.

The behavior of N2 and O2 in pure, mixed or layered CO ices

NASA Astrophysics Data System (ADS)

Bisschop, Suzanne E.; Fraser, Helen J.; Fuchs, Guido; Öberg, Karin I.; Acharyya, Kinsuk; van Broekhuizen, Fleur; Schlemmer, Stephan; van Dishoeck, Ewine F.

N2 and O2 are molecules that are predicted to be abundant in dense molecular clouds. Both molecules are difficult to detect as neither has a dipole moment. The chemical abundance of N2 is mostly inferred from its daughter species N2H+, but was recently detected in the ISM for the first time, with an abundance of 3.3 × 10-7 (Knauth et al 2004). Searches for the submillimeter lines of O2 have given upper limits for the abundance of ≤ 2.6 10-7 for star forming clouds and ≤ 3 10-6 for cold dark clouds (Goldsmith et al. 2000). Pontoppidan et al. (2003) deduced from the CO line profile that CO is present in both H2O poor and H2O rich ice layers, so it follows that N2 is likely to be present in a H2O poor ice layer. In many cold and protostellar cores N2H+ is found to anti-correlate with HCO+ and CO (Bergin et al. 2001; Jørgensen et al. 2004). Models by, for example Bergin & Langer (1997), assume this is due to the balance between freeze-out and evaporation, where ratios for the binding energy for N2 compared to CO of 0.50-0.70 are used. To model these processes, and reproduce the observed abundances of each species it is important to determine empirically the binding energies, sticking probabilities and desorption kinetics of model ice systems containing CO, N2 and O2. It seems that these quantities depend on the degree to which N2 and O2 mix with CO. Therefore, CO and N2 ices were studied extensively in a Ultra High Vacuum (UHV) experiment (P ~ 1 × 10-10 Torr) (Oberg et al. 2005; Bisschop et al submitted)). Ice samples were deposited at 14 K on a polycrystalline gold sample, mounted in the UHV chamber, covering morphologies from pure CO and N2, and 1:1 mixtures, to 1/1 layers of both CO over N2 and N2 over CO, and layers of 40 L of CO (1 L ≈ 1 monolayer) covered with 5 to 50 L of N2. The ices were studied using a combination of Reflection Absorption Infrared Spectroscopy (RAIRS) and Temperature Programmed Desorption (TPD), at a ramp-rate of 0.1 K min-1. The TPD

High-resolution mineral dust and sea ice proxy records from the Talos Dome ice core

NASA Astrophysics Data System (ADS)

Schüpbach, S.; Federer, U.; Kaufmann, P. R.; Albani, S.; Barbante, C.; Stocker, T. F.; Fischer, H.

2013-12-01

In this study we report on new non-sea salt calcium (nssCa2+, mineral dust proxy) and sea salt sodium (ssNa+, sea ice proxy) records along the East Antarctic Talos Dome deep ice core in centennial resolution reaching back 150 thousand years (ka) before present. During glacial conditions nssCa2+ fluxes in Talos Dome are strongly related to temperature as has been observed before in other deep Antarctic ice core records, and has been associated with synchronous changes in the main source region (southern South America) during climate variations in the last glacial. However, during warmer climate conditions Talos Dome mineral dust input is clearly elevated compared to other records mainly due to the contribution of additional local dust sources in the Ross Sea area. Based on a simple transport model, we compare nssCa2+ fluxes of different East Antarctic ice cores. From this multi-site comparison we conclude that changes in transport efficiency or atmospheric lifetime of dust particles do have a minor effect compared to source strength changes on the large-scale concentration changes observed in Antarctic ice cores during climate variations of the past 150 ka. Our transport model applied on ice core data is further validated by climate model data. The availability of multiple East Antarctic nssCa2+ records also allows for a revision of a former estimate on the atmospheric CO2 sensitivity to reduced dust induced iron fertilisation in the Southern Ocean during the transition from the Last Glacial Maximum to the Holocene (T1). While a former estimate based on the EPICA Dome C (EDC) record only suggested 20 ppm, we find that reduced dust induced iron fertilisation in the Southern Ocean may be responsible for up to 40 ppm of the total atmospheric CO2 increase during T1. During the last interglacial, ssNa+ levels of EDC and EPICA Dronning Maud Land (EDML) are only half of the Holocene levels, in line with higher temperatures during that period, indicating much reduced sea

Formation of Glycerol through Hydrogenation of CO Ice under Prestellar Core Conditions

NASA Astrophysics Data System (ADS)

Fedoseev, G.; Chuang, K.-J.; Ioppolo, S.; Qasim, D.; van Dishoeck, E. F.; Linnartz, H.

2017-06-01

Observational studies reveal that complex organic molecules (COMs) can be found in various objects associated with different star formation stages. The identification of COMs in prestellar cores, I.e., cold environments in which thermally induced chemistry can be excluded and radiolysis is limited by cosmic rays and cosmic-ray-induced UV photons, is particularly important as this stage sets up the initial chemical composition from which ultimately stars and planets evolve. Recent laboratory results demonstrate that molecules as complex as glycolaldehyde and ethylene glycol are efficiently formed on icy dust grains via nonenergetic atom addition reactions between accreting H atoms and CO molecules, a process that dominates surface chemistry during the “CO freeze-out stage” in dense cores. In the present study we demonstrate that a similar mechanism results in the formation of the biologically relevant molecule glycerol—HOCH2CH(OH)CH2OH—a three-carbon-bearing sugar alcohol necessary for the formation of membranes of modern living cells and organelles. Our experimental results are fully consistent with a suggested reaction scheme in which glycerol is formed along a chain of radical-radical and radical-molecule interactions between various reactive intermediates produced upon hydrogenation of CO ice or its hydrogenation products. The tentative identification of the chemically related simple sugar glyceraldehyde—HOCH2CH(OH)CHO—is discussed as well. These new laboratory findings indicate that the proposed reaction mechanism holds much potential to form even more complex sugar alcohols and simple sugars.

Sea Ice as a Sink for CO2 and Biogeochemical Material: a Novel Sampling Method and Astrobiological Applications

NASA Astrophysics Data System (ADS)

Wilner, J.; Hofmann, A.; Hand, K. P.

2017-12-01

Accurately modelling the intensification of greenhouse gas effects in the polar regions ("polar amplification") necessitates a thorough understanding of the geochemical balance between atmospheric, sea ice, and oceanic layers. Sea ice is highly permeable to CO2 and therefore represents a major sink of oceanic CO2 in winter and of atmospheric CO2 in summer, sinks that are typically either poorly constrained in or fully absent from global climate models. We present a novel method for sampling both trapped and dissolved gases (CO2, CH4 and δ13CH4) in sea ice with a Picarro 2132-i Methane Analyzer, taking the following sampling considerations into account: minimization of water and air contamination, full headspace sampling, prevention of inadvertent sample bag double-puncturing, and ease of use. This method involves melting of vacuum-sealed ice cores to evacuate trapped gases to the headspace and sampling the headspace gas with a blunt needle sheathed by a beveled puncturing needle. A gravity catchment tube prevents input of dangerous levels of liquid water to the Picarro cavity. Subsequent ultrasonic degassing allows for dissolved gas measurement. We are in the process of using this method to sample gases trapped and dissolved in Arctic autumn sea ice cores and atmospheric samples collected during the 2016 Polarstern Expedition and during a May 2017 field campaign north of Barrow, Alaska. We additionally employ this method, together with inductively coupled plasma mass spectrometry (ICP-MS), to analyze the transfer of potential biogeochemical signatures of underlying hydrothermal plumes to sea ice. This has particular relevance to Europa and Enceladus, where hypothetical hydrothermal plumes may deliver seafloor chemicals to the overlying ice shell. Hence, we are presently investigating the entrainment of methane and other hydrothermal material in sea ice cores collected along the Gakkel Ridge that may serve as biosignatures of methanogenic organisms in seafloor

Studies of proton irradiated H2O + CO2 and H2O + CO ices and analysis of synthesized molecules

NASA Technical Reports Server (NTRS)

Moore, M. H.; Khanna, R.; Donn, B.

1991-01-01

Infrared spectra of H2O + CO2 and H2O + CO ices before and after proton irradiation showed that a major reaction in both mixtures was the interconversion of CO2 yields CO. Radiation synthesized organic compounds such as carbonic acid were identified in the H2O + CO2 ice. Different chemical pathways dominate in the H2O + CO ice in which formaldehyde, methanol, ethanol, and methane were identified. Sublimed material was also analyzed using a mass spectrometer. Implications of these results are discussed in reference to comets.

Quantification of UV stimulated ice chemistry: CO and CO2

NASA Technical Reports Server (NTRS)

Anicich, V. G.; Arakelian, T.; Hanner, M. S.

1991-01-01

Recent laboratory experiments are presented that show that during photolysis of the pure ices there is evidence of the interconversion of CO to CO2 and CO2 to CO using Lyman alpha (1216A) radiation. In addition, there is a substantial amount of another substance being produced. This substance is evident by its infrared absorption peak at 2235 cm(-1). It is believed that this new peak is due to carbon suboxide, C3O2. CO and CO2 have already been detected in comets, and C3O2 has been suggested as a cometary from radiation of CO. Comparisons are made between our results at 1215A and proton radiation experiments and radiation at other wavelengths. The suggestion is that the processing of ices is energy dependent, i.e., dependent on the type of radiation. Several difficult problems have to be solved before these radiation conversions can be quantified. The steps that we are taking to quantify the kinetics are discussed.

Porosity and thermal collapse measurements of H2O, CH3OH, CO2, and H2O:CO2 ices.

PubMed

Isokoski, K; Bossa, J-B; Triemstra, T; Linnartz, H

2014-02-28

The majority of astronomical and laboratory based studies of interstellar ices have been focusing on ice constituents. Ice structure is a much less studied topic. Particularly the amount of porosity is an ongoing point of discussion. A porous ice offers more surface area than a compact ice, for reactions that are fully surface driven. In this paper we discuss the amount of compaction for four different ices--H2O, CH3OH, CO2 and mixed H2O : CO2 = 2 : 1--upon heating over an astronomically relevant temperature regime. Laser interference and Fourier transform infrared spectroscopy are used to confirm that for amorphous solid water the full signal loss of dangling OH bonds is not a proof for full compaction. These data are compared with the first compaction results for pure CH3OH, pure CO2 and mixed H2O : CO2 = 2 : 1 ice. Here we find that thermal segregation benefits from a higher degree of porosity.

First investigations of an ice core from Eisriesenwelt cave (Austria)

NASA Astrophysics Data System (ADS)

May, B.; Spötl, C.; Wagenbach, D.; Dublyansky, Y.; Liebl, J.

2010-09-01

Investigations into the genesis and dynamical properties of cave ice are essential for assessing the climate significance of these underground glaciers. We drilled an ice core through a 7.1 m thick ice body filling a large cavern of the dynamic ice cave Eisenriesenwelt (Austria). In addition to visual core inspections, quasi-continuous measurements at 2 cm resolution comprised particulate matter, stable water isotope (δ18O, δD) and electrolytic conductivity profiles supplemented by specifically selected samples analysed for tritium and radiocarbon. We found that recent ablation led to an almost complete loss of bomb derived tritium removing any ice accumulated, since at least, the early fifties leaving the actual ice surface even below the natural tritium level. The small particulate organic masses made radiocarbon dating inconclusive, though a crude estimate gave a maximum ice age in the order of several thousand years. The visual stratigraphy and all investigated parameters showed a clear dichotomy between the upper 4 m and the bottom 3 m of the core, which points to a substantial change in the ice formation process. Main features of the core comprise the changing appearance and composition of distinct cyro-calcite layers, a extremely low total ion content and a surprisingly high variability of the isotope signature. Co-isotope evaluation (δD versus δ18O) of the core in comparison with data from precipitation and karst spring water clearly indicate that ice formation is governed by (slow) freezing of dripping water.

Detection and monitoring of H2O and CO2 ice clouds on Mars

USGS Publications Warehouse

Bell, J.F.; Calvin, W.M.; Ockert-Bell, M. E.; Crisp, D.; Pollack, James B.; Spencer, J.

1996-01-01

We have developed an observational scheme for the detection and discrimination of Mars atmospheric H2O and CO2 clouds using ground-based instruments in the near infrared. We report the results of our cloud detection and characterization study using Mars near IR images obtained during the 1990 and 1993 oppositions. We focused on specific wavelengths that have the potential, based on previous laboratory studies of H2O and CO2 ices, of yielding the greatest degree of cloud detectability and compositional discriminability. We have detected and mapped absorption features at some of these wavelengths in both the northern and southern polar regions of Mars. Compositional information on the nature of these absorption features was derived from comparisons with laboratory ice spectra and with a simplified radiative transfer model of a CO2 ice cloud overlying a bright surface. Our results indicate that both H2O and CO2 ices can be detected and distinguished in the polar hood clouds. The region near 3.00 ??m is most useful for the detection of water ice clouds because there is a strong H2O ice absorption at this wavelength but only a weak CO2 ice band. The region near 3.33 ??m is most useful for the detection of CO2 ice clouds because there is a strong, relatively narrow CO2 ice band at this wavelength but only broad "continuum" H2O ice absorption. Weaker features near 2.30 ??m could arise from CO2 ice at coarse grain sizes, or surface/dust minerals. Narrow features near 2.00 ??m, which could potentially be very diagnostic of CO2 ice clouds, suffer from contamination by Mars atmospheric CO2 absorptions and are difficult to interpret because of the rather poor knowledge of surface elevation at high latitudes. These results indicate that future ground-based, Earth-orbital, and spacecraft studies over a more extended span of the seasonal cycle should yield substantial information on the style and timing of volatile transport on Mars, as well as a more detailed understanding of

Formation of Glycerol through Hydrogenation of CO Ice under Prestellar Core Conditions

DOE Office of Scientific and Technical Information (OSTI.GOV)

Fedoseev, G.; Chuang, K.-J.; Qasim, D.

Observational studies reveal that complex organic molecules (COMs) can be found in various objects associated with different star formation stages. The identification of COMs in prestellar cores, i.e., cold environments in which thermally induced chemistry can be excluded and radiolysis is limited by cosmic rays and cosmic-ray-induced UV photons, is particularly important as this stage sets up the initial chemical composition from which ultimately stars and planets evolve. Recent laboratory results demonstrate that molecules as complex as glycolaldehyde and ethylene glycol are efficiently formed on icy dust grains via nonenergetic atom addition reactions between accreting H atoms and CO molecules,more » a process that dominates surface chemistry during the “CO freeze-out stage” in dense cores. In the present study we demonstrate that a similar mechanism results in the formation of the biologically relevant molecule glycerol—HOCH{sub 2}CH(OH)CH{sub 2}OH—a three-carbon-bearing sugar alcohol necessary for the formation of membranes of modern living cells and organelles. Our experimental results are fully consistent with a suggested reaction scheme in which glycerol is formed along a chain of radical–radical and radical–molecule interactions between various reactive intermediates produced upon hydrogenation of CO ice or its hydrogenation products. The tentative identification of the chemically related simple sugar glyceraldehyde—HOCH{sub 2}CH(OH)CHO—is discussed as well. These new laboratory findings indicate that the proposed reaction mechanism holds much potential to form even more complex sugar alcohols and simple sugars.« less

An observational search for CO2 ice clouds on Mars

NASA Technical Reports Server (NTRS)

Bell, James F., III; Calvin, Wendy M.; Pollack, James B.; Crisp, David

1993-01-01

CO2 ice clouds were first directly identified on Mars by the Mariner 6 and 7 infrared spectrometer limb scans. These observations provided support for early theoretical modeling efforts of CO2 condensation. Mariner 9 IRIS temperature profiles of north polar hood clouds were interpreted as indicating that these clouds were composed of H2O ice at lower latitudes and CO2 ice at higher latitudes. The role of CO2 condensation on Mars has recently received increased attention because (1) Kasting's model results indicated that CO2 cloud condensation limits the magnitude of the proposed early Mars CO2/H2O greenhouse, and (2) Pollack el al.'s GCM results indicated that the formation of CO2 ice clouds is favorable at all polar latitudes during the fall and winter seasons. These latter authors have shown that CO2 clouds play an important role in the polar energy balance, as the amount of CO2 contained in the polar caps is constrained by a balance between latent heat release, heat advected from lower latitudes, and thermal emission to space. The polar hood clouds reduce the amount of CO2 condensation on the polar caps because they reduce the net emission to space. There have been many extensive laboratory spectroscopic studies of H2O and CO2 ices and frosts. In this study, we use results from these and other sources to search for the occurrence of diagnostic CO2 (and H2O) ice and/or frost absorption features in ground based near-infrared imaging spectroscopic data of Mars. Our primary goals are (1) to try to confirm the previous direct observations of CO2 clouds on Mars; (2) to determine the spatial extent, temporal variability, and composition (H2O/CO2 ratio) of any clouds detected; and (3) through radiative transfer modeling, to try to determine the mean particle size and optical depth of polar hood clouds, thus, assessing their role in the polar heat budget.

An Optical Dye Method for Continuous Determination of Acidity in Ice Cores.

PubMed

Kjær, Helle Astrid; Vallelonga, Paul; Svensson, Anders; Elleskov L Kristensen, Magnus; Tibuleac, Catalin; Winstrup, Mai; Kipfstuhl, Sepp

2016-10-04

The pH of polar ice is important for the stability and mobility of impurities in ice cores and can be strongly influenced by volcanic eruptions or anthropogenic emissions. We present a simple optical method for continuous determination of acidity in ice cores based on spectroscopically determined color changes of two common pH-indicator dyes, bromophenol blue, and chlorophenol red. The sealed-system method described here is not equilibrated with CO 2 , making it simpler than existing methods for pH determination in ice cores and offering a 10-90% peak response time of 45 s and a combined uncertainty of 9%. The method is applied to Holocene ice core sections from Greenland and Antarctica and compared to standard techniques such as electrical conductivity measurement (ECM) conducted on the solid ice, and electrolytic meltwater conductivity, EMWC. Acidity measured in the Greenland NGRIP ice core shows good agreement with acidity calculated from ion chromatography. Conductivity and dye-based acidity H dye + are found to be highly correlated in the Greenland NEGIS firn core (75.38° N, 35.56° W), with all signals greater than 3σ variability coinciding with either volcanic eruptions or possible wild fire activity. In contrast, the Antarctic Roosevelt Island ice core (79.36° S, 161.71° W) features an anticorrelation between conductivity and H dye + , likely due to strong influence of marine salts.

Visual-Stratigraphic Dating of the GISP2 Ice Core: Basis, Reproducibility, and Application

NASA Technical Reports Server (NTRS)

Alley, R. B.; Shuman, C. A.; Meese, D. A.; Gow, A. J.; Taylor, K. C.; Cuffey, K. M.; Fitzpatrick, J. J.; Grootes, P. M.; Zielinski, G. A.; Ram, M.;

Visual-stratigraphic dating of the GISP2 ice core: Basis, reproducibility, and application

NASA Astrophysics Data System (ADS)

Alley, R. B.; Shuman, C. A.; Meese, D. A.; Gow, A. J.; Taylor, K. C.; Cuffey, K. M.; Fitzpatrick, J. J.; Grootes, P. M.; Zielinski, G. A.; Ram, M.; Spinelli, G.; Elder, B.

1997-11-01

Annual layers are visible in the Greenland Ice Sheet Project 2 ice core from central Greenland, allowing rapid dating of the core. Changes in bubble and grain structure caused by near-surface, primarily summertime formation of hoar complexes provide the main visible annual marker in the Holocene, and changes in "cloudiness" of the ice correlated with dustiness mark Wisconsinan annual cycles; both markers are evident and have been intercalibrated in early Holocene ice. Layer counts are reproducible between different workers and for one worker at different times, with 1% error over century-length times in the Holocene. Reproducibility is typically 5% in Wisconsinan ice-age ice and decreases with increasing age and depth. Cumulative ages from visible stratigraphy are not significantly different from independent ages of prominent events for ice older than the historical record and younger than approximately 50,000 years. Visible observations are not greatly degraded by "brittle ice" or many other core-quality problems, allowing construction of long, consistently sampled time series. High accuracy requires careful study of the core by dedicated observers.

Holocene Accumulation and Ice Flow near the West Antarctic Ice Sheet Divide Ice Core Site

NASA Technical Reports Server (NTRS)

Koutnik, Michelle R.; Fudge, T.J.; Conway, Howard; Waddington, Edwin D.; Neumann, Thomas A.; Cuffey, Kurt M.; Buizert, Christo; Taylor, Kendrick C.

2016-01-01

The West Antarctic Ice Sheet Divide Core (WDC) provided a high-resolution climate record from near the Ross-Amundsen Divide in Central West Antarctica. In addition, radar-detected internal layers in the vicinity of the WDC site have been dated directly from the ice core to provide spatial variations in the age structure of the region. Using these two data sets together, we first infer a high-resolution Holocene accumulation-rate history from 9.2 thousand years of the ice-core timescale and then confirm that this climate history is consistent with internal layers upstream of the core site. Even though the WDC was drilled only 24 kilometers from the modern ice divide, advection of ice from upstream must be taken into account. We evaluate histories of accumulation rate by using a flowband model to generate internal layers that we compare to observed layers. Results show that the centennially averaged accumulation rate was over 20 percent lower than modern at 9.2 thousand years before present (B.P.), increased by 40 percent from 9.2 to 2.3 thousand years B.P., and decreased by at least 10 percent over the past 2 thousand years B.P. to the modern values; these Holocene accumulation-rate changes in Central West Antarctica are larger than changes inferred from East Antarctic ice-core records. Despite significant changes in accumulation rate, throughout the Holocene the regional accumulation pattern has likely remained similar to today, and the ice-divide position has likely remained on average within 5 kilometers of its modern position. Continent-scale ice-sheet models used for reconstructions of West Antarctic ice volume should incorporate this accumulation history.

CO-ices in embedded Young Stellar Objects

NASA Astrophysics Data System (ADS)

Teixeira, Teresa Cláeira V. S.

1998-09-01

Stars are born in dense cores within molecular clouds, enshrouded in large cocoons of gas and dust which completely obscure the forming star. The large degree of obscuration towards the young stars is due to the presence of solid dust grains in their circumstellar envelopes, which efficiently absorb the radiation from the star at visual and ultraviolet wavelengths, reradiating that energy at far-infrared and submillimeter wavelengths. The composition and structure of the dust grains is not well known, but current studies point to grains having a refractory core and acquiring ice mantles in the cool, shielded conditions of molecular clouds. Such ice mantles are the subject of this thesis. Infrared spectroscopy is an important tool in the study of the complex ice mantles on interstellar grains. A variety of absorption features at these wavelengths, which have been identified as the vibrational transitions of the molecules in the ices, can provide important information on the composition, structure and evolution of the grains. The work reported in this thesis consists of an observational study of the composition of the ice mantles acquired by the dust grains in molecular clouds (with particular emphasis on the CO-ices in the material surrounding embedded Young Stellar Objects in nearby molecular clouds), what can be learned from that about the physical conditions in the regions where the ice mantles exist, and what may affect their survival and evolution. In this work, spectra of the 4.67 micron solid CO absorption feature are presented, mostly towards embedded objects in Taurus. The thesis starts with a brief overview of technical aspects of spectroscopic observations at thermal infrared wavelengths, where the CO stretch absorption feature is located. The observations and data reduction procedures are then reported and discussed in detail. The likely composition of the CO-bearing ices is analysed by fitting the observations with laboratory data. The statistical

CO2 jets formed by sublimation beneath translucent slab ice in Mars' seasonal south polar ice cap

USGS Publications Warehouse

Kieffer, H.H.; Christensen, P.R.; Titus, T.N.

2006-01-01

The martian polar caps are among the most dynamic regions on Mars, growing substantially in winter as a significant fraction of the atmosphere freezes out in the form of CO2 ice. Unusual dark spots, fans and blotches form as the south-polar seasonal CO2 ice cap retreats during spring and summer. Small radial channel networks are often associated with the location of spots once the ice disappears. The spots have been proposed to be simply bare, defrosted ground; the formation of the channels has remained uncertain. Here we report infrared and visible observations that show that the spots and fans remain at CO2 ice temperatures well into summer, and must be granular materials that have been brought up to the surface of the ice, requiring a complex suite of processes to get them there. We propose that the seasonal ice cap forms an impermeable, translucent slab of CO2 ice that sublimates from the base, building up high-pressure gas beneath the slab. This gas levitates the ice, which eventually ruptures, producing high-velocity CO 2 vents that erupt sand-sized grains in jets to form the spots and erode the channels. These processes are unlike any observed on Earth. ?? 2006 Nature Publishing Group.

Ice Core Investigations

ERIC Educational Resources Information Center

Krim, Jessica; Brody, Michael

2008-01-01

What can glaciers tell us about volcanoes and atmospheric conditions? How does this information relate to our understanding of climate change? Ice Core Investigations is an original and innovative activity that explores these types of questions. It brings together popular science issues such as research, climate change, ice core drilling, and air…

Ice Core Records of Recent Northwest Greenland Climate

NASA Astrophysics Data System (ADS)

Osterberg, E. C.; Wong, G. J.; Ferris, D.; Lutz, E.; Howley, J. A.; Kelly, M. A.; Axford, Y.; Hawley, R. L.

2014-12-01

Meteorological station data from NW Greenland indicate a 3oC temperature rise since 1990, with most of the warming occurring in fall and winter. According to remote sensing data, the NW Greenland ice sheet (GIS) and coastal ice caps are responding with ice mass loss and margin retreat, but the cryosphere's response to previous climate variability is poorly constrained in this region. We are developing multi-proxy records (lake sediment cores, ice cores, glacial geologic data, glaciological models) of Holocene climate change and cryospheric response in NW Greenland to improve projections of future ice loss and sea level rise in a warming climate. As part of our efforts to develop a millennial-length ice core paleoclimate record from the Thule region, we collected and analyzed snow pit samples and short firn cores (up to 21 m) from the coastal region of the GIS (2Barrel site; 76.9317o N, 63.1467o W, 1685 m el.) and the summit of North Ice Cap (76.938o N, 67.671o W, 1273 m el.) in 2011, 2012 and 2014. The 2Barrel ice core record has statistically significant relationships with regional spring and fall Baffin Bay sea ice extent, summertime temperature, and annual precipitation. Here we evaluate relationships between the 2014 North Ice Cap firn core glaciochemical record and climate variability from regional instrumental stations and reanalysis datasets. We compare the coastal North Ice Cap record to more inland records from 2Barrel, Camp Century and NEEM to evaluate spatial and elevational gradients in recent NW Greenland climate change.

Observed Arctic sea-ice loss directly follows anthropogenic CO2 emission.

PubMed

Notz, Dirk; Stroeve, Julienne

2016-11-11

Arctic sea ice is retreating rapidly, raising prospects of a future ice-free Arctic Ocean during summer. Because climate-model simulations of the sea-ice loss differ substantially, we used a robust linear relationship between monthly-mean September sea-ice area and cumulative carbon dioxide (CO 2 ) emissions to infer the future evolution of Arctic summer sea ice directly from the observational record. The observed linear relationship implies a sustained loss of 3 ± 0.3 square meters of September sea-ice area per metric ton of CO 2 emission. On the basis of this sensitivity, Arctic sea ice will be lost throughout September for an additional 1000 gigatons of CO 2 emissions. Most models show a lower sensitivity, which is possibly linked to an underestimation of the modeled increase in incoming longwave radiation and of the modeled transient climate response. Copyright © 2016, American Association for the Advancement of Science.

CO2 (dry ice) cleaning system

NASA Technical Reports Server (NTRS)

Barnett, Donald M.

1995-01-01

Tomco Equipment Company has participated in the dry ice (solid carbon dioxide, CO2) cleaning industry for over ten years as a pioneer in the manufacturer of high density, dry ice cleaning pellet production equipment. For over four years Tomco high density pelletizers have been available to the dry ice cleaning industry. Approximately one year ago Tomco introduced the DI-250, a new dry ice blast unit making Tomco a single source supplier for sublimable media, particle blast, cleaning systems. This new blast unit is an all pneumatic, single discharge hose device. It meters the insertion of 1/8 inch diameter (or smaller), high density, dry ice pellets into a high pressure, propellant gas stream. The dry ice and propellant streams are controlled and mixed from the blast cabinet. From there the mixture is transported to the nozzle where the pellets are accelerated to an appropriate blasting velocity. When directed to impact upon a target area, these dry ice pellets have sufficient energy to effectively remove most surface coatings through dry, abrasive contact. The meta-stable, dry ice pellets used for CO2 cleaning, while labeled 'high density,' are less dense than alternate, abrasive, particle blast media. In addition, after contacting the target surface, they return to their equilibrium condition: a superheated gas state. Most currently used grit blasting media are silicon dioxide based, which possess a sharp tetrahedral molecular structure. Silicon dioxide crystal structures will always produce smaller sharp-edged replicas of the original crystal upon fracture. Larger, softer dry ice pellets do not share the same sharp-edged crystalline structures as their non-sublimable counterparts when broken. In fact, upon contact with the target surface, dry ice pellets will plastically deform and break apart. As such, dry ice cleaning is less harmful to sensitive substrates, workers and the environment than chemical or abrasive cleaning systems. Dry ice cleaning system

Climatic Changes on Tibetan Plateau Based on Ice Core Records

NASA Astrophysics Data System (ADS)

Yao, T.

2008-12-01

Climatic changes have been reconstructed for the Tibetan Plateau based on ice core records. The Guliya ice core on the Tibetan Plateau presents climatic changes in the past 100,000 years, thus is comparative with that from Vostok ice core in Antarctica and GISP2 record in Arctic. These three records share an important common feature, i.e., our climate is not stable. It is also evident that the major patterns of climatic changes are similar on the earth. Why does climatic change over the earth follow a same pattern? It might be attributed to solar radiation. We found that the cold periods correspond to low insolation periods, and warm periods to high insolation periods. We found abrupt climatic change in the ice core climatic records, which presented dramatic temperature variation of as much as 10 °C in 50 or 60 years. Our major challenge in the study of both climate and environment is that greenhouse gases such as CO2, CH4 are possibly amplifying global warming, though at what degree remains unclear. One of the ways to understand the role of greenhouse gases is to reconstruct the past greenhouse gases recorded in ice. In 1997, we drilled an ice core from 7100 m a.s.l. in the Himalayas to reconstruct methane record. Based on the record, we found seasonal cycles in methane variation. In particular, the methane concentration is high in summer, suggestiing active methane emission from wet land in summer. Based on the seasonal cycle, we can reconstruct the methane fluctuation history in the past 500 years. The most prominent feature of the methane record in the Himalayan ice core is the abrupt increase since 1850 A.D.. This is closely related to the industrial revolution worldwide. We can also observe sudden decrease in methane concentration during the World War I and World War II. It implies that the industrial revolution has dominated the atmospheric greenhouse gas emission for about 100 years. Besides, the average methane concentration in the Himalayan ice core is

Greenhouse Gas Concentration Records Extended Back to 800,000 Years From the EPICA Dome C Ice Core

NASA Astrophysics Data System (ADS)

Chappellaz, J.; Luethi, D.; Loulergue, L.; Barnola, J.; Bereiter, B.; Blunier, T.; Jouzel, J.; Lefloch, M.; Lemieux, B.; Masson-Delmotte, V.; Raynaud, D.; Schilt, A.; Siegenthaler, U.; Spahni, R.; Stocker, T.

2007-12-01

The deep ice core recovered from Dome Concordia in the framework of EPICA, the European Project for Ice Coring in Antarctica, has extended the record of Antarctic climate history back to 800,000 years [Jouzel et al., 2007]. We present the current status of measurements of CO2, CH4 and N2O on air trapped in the bubbles of the Dome C ice core. CO2 is measured in two laboratories using different techniques (laser absorption spectroscopy or gas chromatography on samples of 8 and 40 g of ice which are mechanically crushed or milled, respectively). CH4 and N2O are extracted using a melt-refreeze technique and then measured by gas chromatography (in two laboratories for CH4). The greenhouse gas concentrations have now been measured on the lowest 200 m of the Dome C core, going back to Marine Isotope Stage 20 (MIS 20) as verified by a consistent gas age/ice age difference determined at termination IX [Jouzel et al., 2007]. The atmospheric CO2 concentration mostly lagged the Antarctic temperature with a rather strong correlation throughout the eight and a half glacial cycles, but with significantly lower CO2 values between 650 and 750 kyr BP. Its lowest level ever measured in ice cores (172 ppmv) is observed during MIS 16 (minimum centered at 667 kyr BP according to the EDC3 chronology) redetermining the natural span of CO2 to 172-300 ppmv. With 2245 individual measurements, the CH4 concentration is now reconstructed over 800,000 years from a single core, with an average time resolution of 380 years. Spectral analyses of the CH4 signal show an increasing contribution of precession during the last four climatic cycles compared with the four older ones, suggesting an increasing impact of low latitudes sources/sinks. Millennial scale features in this very detailed signal allows us to compare their occurrence with ice volume reconstructions and the isotopic composition of precipitation over the East Antarctic plateau. N2O is still affected by glaciological artefacts involving

Effects of sea-ice and biogeochemical processes and storms on under-ice water fCO2 during the winter-spring transition in the high Arctic Ocean: Implications for sea-air CO2 fluxes

NASA Astrophysics Data System (ADS)

Fransson, Agneta; Chierici, Melissa; Skjelvan, Ingunn; Olsen, Are; Assmy, Philipp; Peterson, Algot K.; Spreen, Gunnar; Ward, Brian

2017-07-01

We performed measurements of carbon dioxide fugacity (fCO2) in the surface water under Arctic sea ice from January to June 2015 during the Norwegian young sea ICE (N-ICE2015) expedition. Over this period, the ship drifted with four different ice floes and covered the deep Nansen Basin, the slopes north of Svalbard, and the Yermak Plateau. This unique winter-to-spring data set includes the first winter-time under-ice water fCO2 observations in this region. The observed under-ice fCO2 ranged between 315 µatm in winter and 153 µatm in spring, hence was undersaturated relative to the atmospheric fCO2. Although the sea ice partly prevented direct CO2 exchange between ocean and atmosphere, frequently occurring leads and breakup of the ice sheet promoted sea-air CO2 fluxes. The CO2 sink varied between 0.3 and 86 mmol C m-2 d-1, depending strongly on the open-water fractions (OW) and storm events. The maximum sea-air CO2 fluxes occurred during storm events in February and June. In winter, the main drivers of the change in under-ice water fCO2 were dissolution of CaCO3 (ikaite) and vertical mixing. In June, in addition to these processes, primary production and sea-air CO2 fluxes were important. The cumulative loss due to CaCO3 dissolution of 0.7 mol C m-2 in the upper 10 m played a major role in sustaining the undersaturation of fCO2 during the entire study. The relative effects of the total fCO2 change due to CaCO3 dissolution was 38%, primary production 26%, vertical mixing 16%, sea-air CO2 fluxes 16%, and temperature and salinity insignificant.

Laboratory Investigations of Physical State of CO2 Ice on Mars

NASA Astrophysics Data System (ADS)

Portyankina, G.; Merrison, J.; Iversen, J. J.; Yoldi, Z.; Hansen, C. J.; Aye, K.-M.; Pommeroll, A.

2016-09-01

We used Environmental Wind Tunnel to simulate CO2 ice condensation under the conditions of the martian polar areas. We find that under conditions usual for martian fall and winter, CO2 ice always deposits from atmosphere as a translucent slab.

H-implantation in SO 2 and CO 2 ices

NASA Astrophysics Data System (ADS)

Garozzo, M.; Fulvio, D.; Gomis, O.; Palumbo, M. E.; Strazzulla, G.

2008-07-01

Ices in the solar system are observed on the surface of planets, satellites, comets and asteroids where they are continuously subordinate at particle fluxes (cosmic ions, solar wind and charged particles caught in the magnetosphere of the planets) that deeply modify their physical and structural properties. Each incoming ion destroys molecular bonds producing fragments that, by recombination, form new molecules also different from the original ones. Moreover, if the incoming ion is reactive (H +, O n+ , S n+ , etc.), it can concur to the formation of new molecules. Those effects can be studied by laboratory experiments where, with some limitation, it is possible to reproduce the astrophysical environments of planetary ices. In this work, we describe some experiments of 15-100 keV H + and He + implantation in pure sulfur dioxide (SO 2) at 16 and 80 K and carbon dioxide (CO 2) at 16 K ices aimed to search for the formation of new molecules. Among other results we confirm that carbonic acid (H 2CO 3) is formed after H-implantation in CO 2, vice versa H-implantation in SO 2 at both temperatures does not produce measurable quantity of sulfurous acid (H 2SO 3). The results are discussed in the light of their relevance to the chemistry of some solar system objects, particularly of Io, the innermost of Jupiter's Galilean satellites, that exhibits a surface very rich in frost SO 2 and it is continuously bombarded with H + ions caught in Jupiter's magnetosphere.

A common and optimized age scale for Antarctic ice cores

NASA Astrophysics Data System (ADS)

Parrenin, F.; Veres, D.; Landais, A.; Bazin, L.; Lemieux-Dudon, B.; Toye Mahamadou Kele, H.; Wolff, E.; Martinerie, P.

2012-04-01

Dating ice cores is a complex problem because 1) there is a age shift between the gas bubbles and the surrounding ice 2) there are many different ice cores which can be synchronized with various proxies and 3) there are many methods to date the ice and the gas bubbles, each with advantages and drawbacks. These methods fall into the following categories: 1) Ice flow (for the ice) and firn densification modelling (for the gas bubbles); 2) Comparison of ice core proxies with insolation variations (so-called orbital tuning methods); 3) Comparison of ice core proxies with other well dated archives; 4) Identification of well-dated horizons, such as tephra layers or geomagnetic anomalies. Recently, an new dating tool has been developped (DATICE, Lemieux-Dudon et al., 2010), to take into account all the different dating information into account and produce a common and optimal chronology for ice cores with estimated confidence intervals. In this talk we will review the different dating information for Antarctic ice cores and show how the DATICE tool can be applied.

CO2 flux over young and snow-covered Arctic pack ice in winter and spring

NASA Astrophysics Data System (ADS)

Nomura, Daiki; Granskog, Mats A.; Fransson, Agneta; Chierici, Melissa; Silyakova, Anna; Ohshima, Kay I.; Cohen, Lana; Delille, Bruno; Hudson, Stephen R.; Dieckmann, Gerhard S.

2018-06-01

Rare CO2 flux measurements from Arctic pack ice show that two types of ice contribute to the release of CO2 from the ice to the atmosphere during winter and spring: young, thin ice with a thin layer of snow and older (several weeks), thicker ice with thick snow cover. Young, thin sea ice is characterized by high salinity and high porosity, and snow-covered thick ice remains relatively warm ( > -7.5 °C) due to the insulating snow cover despite air temperatures as low as -40 °C. Therefore, brine volume fractions of these two ice types are high enough to provide favorable conditions for gas exchange between sea ice and the atmosphere even in mid-winter. Although the potential CO2 flux from sea ice decreased due to the presence of the snow, the snow surface is still a CO2 source to the atmosphere for low snow density and thin snow conditions. We found that young sea ice that is formed in leads without snow cover produces CO2 fluxes an order of magnitude higher than those in snow-covered older ice (+1.0 ± 0.6 mmol C m-2 day-1 for young ice and +0.2 ± 0.2 mmol C m-2 day-1 for older ice).

Raman spectroscopy on ice cores from Greenland and Antarctica

NASA Astrophysics Data System (ADS)

Weikusat, C.; Kipfstuhl, S.

2012-04-01

Ice cores are invaluable archives for the reconstruction of the climatic history of the earth. Besides the analysis of various climatic processes from isotopes and chemical signatures they offer the unique possibility of directly extracting the past atmosphere from gaseous inclusions in the ice. Many aspects of the formation and alterations of these inclusions, e.g. the entrapment of air at the firn-ice-transition, the formation of crystalline gas hydrates (clathrates) from the bubbles or the structural relaxation during storage of the cores, need to be better understood to enable reliable interpretations of the obtained data. Modern micro Raman spectroscopy is an excellent tool to obtain high-quality data for all of these aspects. It has been productively used for phase identification of solid inclusions [1], investigation of air clathrates [2] and high-resolution measurements of N2/O2 mixing ratios inside individual air bubbles [3,4]. Detailed examples of the various uses of Raman spectroscopy will be presented along with practical information about the techniques required to obtain high-quality spectra. Retrieval and interpretation of quantitative data from the spectra will be explained. Future possibilities for advanced uses of Raman spectroscopy for ice core research will be discussed. [1] T. Sakurai et al., 2009, Direct observation of salts as micro-inclusions in the Greenland GRIP ice core. Journal of Glaciology, 55, 777-783. [2] F. Pauer et al., 1995, Raman spectroscopic study of nitrogen/oxygen ratio in natural ice clathrates in the GRIP ice core. Geophysical Research Letters, 22, 969-971. [3] T. Ikeda-Fukazawa et al., 2001, Variation in N2/O2 ratio of occluded air in Dome Fuji antarctic ice. Journal of Geophysical Research, 106, 17799-17810. [4] C. Weikusat et al., Raman spectroscopy of gaseous inclusions in EDML ice core: First results - microbubbles. Journal of Glaciology, accepted.

Making an Ice Core.

ERIC Educational Resources Information Center

Kopaska-Merkel, David C.

1995-01-01

Explains an activity in which students construct a simulated ice core. Materials required include only a freezer, food coloring, a bottle, and water. This hands-on exercise demonstrates how a glacier is formed, how ice cores are studied, and the nature of precision and accuracy in measurement. Suitable for grades three through eight. (Author/PVD)

The Role of Sea Ice in 2 x CO2 Climate Model Sensitivity. Part 2; Hemispheric Dependencies

NASA Technical Reports Server (NTRS)

Rind, D.; Healy, R.; Parkinson, C.; Martinson, D.

1997-01-01

How sensitive are doubled CO2 simulations to GCM control-run sea ice thickness and extent? This issue is examined in a series of 10 control-run simulations with different sea ice and corresponding doubled CO2 simulations. Results show that with increased control-run sea ice coverage in the Southern Hemisphere, temperature sensitivity with climate change is enhanced, while there is little effect on temperature sensitivity of (reasonable) variations in control-run sea ice thickness. In the Northern Hemisphere the situation is reversed: sea ice thickness is the key parameter, while (reasonable) variations in control-run sea ice coverage are of less importance. In both cases, the quantity of sea ice that can be removed in the warmer climate is the determining factor. Overall, the Southern Hemisphere sea ice coverage change had a larger impact on global temperature, because Northern Hemisphere sea ice was sufficiently thick to limit its response to doubled CO2, and sea ice changes generally occurred at higher latitudes, reducing the sea ice-albedo feedback. In both these experiments and earlier ones in which sea ice was not allowed to change, the model displayed a sensitivity of -0.02 C global warming per percent change in Southern Hemisphere sea ice coverage.

On the nature of the dirty ice at the bottom of the GISP2 ice core

USGS Publications Warehouse

Bender, Michael L.; Burgess, Edward; Alley, Richard B.; Barnett, Bruce; Clow, Gary D.

2010-01-01

We present data on the triple Ar isotope composition in trapped gas from clean, stratigraphically disturbed ice between 2800 and 3040m depth in the GISP2 ice core, and from basal dirty ice from 3040 to 3053m depth. We also present data for the abundance and isotopic composition of O2 and N2, and abundance of Ar, in the basal dirty ice. The Ar/N2 ratio of dirty basal ice, the heavy isotope enrichment (reflecting gravitational fractionation), and the total gas content all indicate that the gases in basal dirty ice originate from the assimilation of clean ice of the overlying glacier, which comprises most of the ice in the dirty bottom layer. O2 is partly to completely depleted in basal ice, reflecting active metabolism. The gravitationally corrected ratio of 40Ar/38Ar, which decreases with age in the global atmosphere, is compatible with an age of 100-250ka for clean disturbed ice. In basal ice, 40Ar is present in excess due to injection of radiogenic 40Ar produced in the underlying continental crust. The weak depth gradient of 40Ar in the dirty basal ice, and the distribution of dirt, indicate mixing within the basal ice, while various published lines of evidence indicate mixing within the overlying clean, disturbed ice. Excess CH4, which reaches thousands of ppm in basal dirty ice at GRIP, is virtually absent in overlying clean disturbed ice, demonstrating that mixing of dirty basal ice into the overlying clean ice, if it occurs at all, is very slow. Order-of-magnitude estimates indicate that the mixing rate of clean ice into dirty ice is sufficient to maintain a steady thickness of dirty ice against thinning from the mean ice flow. The dirty ice appears to consist of two or more basal components in addition to clean glacial ice. A small amount of soil or permafrost, plus preglacial snow, lake or ground ice could explain the observations.

A review of sea ice proxy information from polar ice cores

NASA Astrophysics Data System (ADS)

Abram, Nerilie J.; Wolff, Eric W.; Curran, Mark A. J.

2013-11-01

Sea ice plays an important role in Earth's climate system. The lack of direct indications of past sea ice coverage, however, means that there is limited knowledge of the sensitivity and rate at which sea ice dynamics are involved in amplifying climate changes. As such, there is a need to develop new proxy records for reconstructing past sea ice conditions. Here we review the advances that have been made in using chemical tracers preserved in ice cores to determine past changes in sea ice cover around Antarctica. Ice core records of sea salt concentration show promise for revealing patterns of sea ice extent particularly over glacial-interglacial time scales. In the coldest climates, however, the sea salt signal appears to lose sensitivity and further work is required to determine how this proxy can be developed into a quantitative sea ice indicator. Methane sulphonic acid (MSA) in near-coastal ice cores has been used to reconstruct quantified changes and interannual variability in sea ice extent over shorter time scales spanning the last ˜160 years, and has potential to be extended to produce records of Antarctic sea ice changes throughout the Holocene. However the MSA ice core proxy also requires careful site assessment and interpretation alongside other palaeoclimate indicators to ensure reconstructions are not biased by non-sea ice factors, and we summarise some recommended strategies for the further development of sea ice histories from ice core MSA. For both proxies the limited information about the production and transfer of chemical markers from the sea ice zone to the Antarctic ice sheets remains an issue that requires further multidisciplinary study. Despite some exploratory and statistical work, the application of either proxy as an indicator of sea ice change in the Arctic also remains largely unknown. As information about these new ice core proxies builds, so too does the potential to develop a more comprehensive understanding of past changes in sea

Mesospheric CO2 ice clouds on Mars observed by Planetary Fourier Spectrometer onboard Mars Express

NASA Astrophysics Data System (ADS)

Aoki, S.; Sato, Y.; Giuranna, M.; Wolkenberg, P.; Sato, T. M.; Nakagawa, H.; Kasaba, Y.

2018-03-01

We have investigated mesospheric CO2 ice clouds on Mars through analysis of near-infrared spectra acquired by Planetary Fourier Spectrometer (PFS) onboard the Mars Express (MEx) from MY 27 to MY 32. With the highest spectral resolution achieved thus far in the relevant spectral range among remote-sensing experiments orbiting Mars, PFS enables precise identification of the scattering peak of CO2 ice at the bottom of the 4.3 μm CO2 band. A total of 111 occurrences of CO2 ice cloud features have been detected over the period investigated. Data from the OMEGA imaging spectrometer onboard MEx confirm all of PFS detections from times when OMEGA operated simultaneously with PFS. The spatial and seasonal distributions of the CO2 ice clouds detected by PFS are consistent with previous observations by other instruments. We find CO2 ice clouds between Ls = 0° and 140° in distinct longitudinal corridors around the equatorial region (± 20°N). Moreover, CO2 ice clouds were preferentially detected at the observational LT range between 15-16 h in MY 29. However, observational biases prevent from distinguishing local time dependency from inter-annual variation. PFS also enables us to investigate the shape of mesospheric CO2 ice cloud spectral features in detail. In all cases, peaks were found between 4.240 and 4.265 μm. Relatively small secondary peaks were occasionally observed around 4.28 μm (8 occurrences). These spectral features cannot be reproduced using our radiative transfer model, which may be because the available CO2 ice refractive indices are inappropriate for the mesospheric temperatures of Mars, or because of the assumption in our model that the CO2 ice crystals are spherical and composed by pure CO2 ice.

Solving the riddle of interglacial temperatures over the last 1.5 million years with a future IPICS "Oldest Ice" ice core

NASA Astrophysics Data System (ADS)

Fischer, Hubertus

2014-05-01

The sequence of the last 8 glacial cycles is characterized by irregular 100,000 year cycles in temperature and sea level. In contrast, the time period between 1.5-1.2 million years ago is characterized by more regular cycles with an obliquity periodicity of 41,000 years. Based on a deconvolution of deep ocean temperature and ice volume contributions to benthic δ18O (Elderfield et al., Science, 2012), it is suggested that glacial sea level became progressively lower over the last 1.5 Myr, while glacial deep ocean temperatures were very similar. At the same time many interglacials prior to the Mid Brunhes event showed significantly cooler deep ocean temperatures than the Holocene, while at the same time interglacial ice volume remained essentially the same. In contrast, interglacial sea surface temperatures in the tropics changed little (Herbert et al., Science,2010) and proxy reconstructions of atmospheric CO2 using δ11B in planktic foraminifera (Hönisch et al., Science, 2009) suggest that prior to 900,000 yr before present interglacial CO2 levels did not differ substantially from those over the last 450,000 years. Accordingly, the conundrum arises how interglacials can differ in deep ocean temperature without any obvious change in ice volume or greenhouse gas forcing and what caused the change in cyclicity of glacial interglacial cycles over the Mid Pleistocene Transition. Probably the most important contribution to solve this riddle is the recovery of a 1.5 Myr old ice core from Antarctica, which among others would provide an unambiguous, high-resolution record of the greenhouse gas history over this time period. Accordingly, the international ice core community, as represented by the International Partnership for Ice Core Science (IPICS), has identified such an 'Oldest Ice' ice core as one of the most important scientific targets for the future (http://www.pages.unibe.ch/ipics/white-papers). However, finding stratigraphically undisturbed ice, which covers this

The physical and infrared spectral properties of CO2 in astrophysical ice analogs

NASA Technical Reports Server (NTRS)

Sandford, S. A.; Allamandola, L. J.

1990-01-01

Results of measurements of the infrared spectroscopic and condensation-vaporization properties of CO2 in pure and mixed ices are presented. Detailed examination of five infrared CO2 bands, 2.20, 2.78, 4.27, 15.2, and 4.39 microns, shows that the peak position, FWHM, and profile of the bands provide important information about the composition, formation, and subsequent thermal history of the ices. Absorption coefficients and their temperature dependence for all five CO2 bands are determined. The temperature dependence variation is found to be less than 15 percent from 10 to 150 K, i.e., the temperature at which H2O ice sublimes. The number of parameters associated with the physical behavior of CO2 in CO2- and H2O-rich ices, including surface binding energies, and condensation and sublimation temperatures, are determined under experimental conditions. The implications of the data obtained for cometary models are considered.

Measurements of ethane in Antarctic ice cores

NASA Astrophysics Data System (ADS)

Verhulst, K. R.; Fosse, E. K.; Aydin, K. M.; Saltzman, E. S.

2011-12-01

Ethane is one of the most abundant hydrocarbons in the atmosphere. The major ethane sources are fossil fuel production and use, biofuel combustion, and biomass-burning emissions and the primary loss pathway is via reaction with OH. A paleoatmospheric ethane record would be useful as a tracer of biomass-burning emissions, providing a constraint on past changes in atmospheric methane and methane isotopes. An independent biomass-burning tracer would improve our understanding of the relationship between biomass burning and climate. The mean annual atmospheric ethane level at high southern latitudes is about 230 parts per trillion (ppt), and Antarctic firn air measurements suggest that atmospheric ethane levels in the early 20th century were considerably lower (Aydin et al., 2011). In this study, we present preliminary measurements of ethane (C2H6) in Antarctic ice core samples with gas ages ranging from 0-1900 C.E. Samples were obtained from dry-drilled ice cores from South Pole and Vostok in East Antarctica, and from the West Antarctic Ice Sheet Divide (WAIS-D). Gases were extracted from the ice by melting under vacuum in a glass vessel sealed by indium wire and were analyzed using high resolution GC/MS with isotope dilution. Ethane levels measured in ice core samples were in the range 100-220 ppt, with a mean of 157 ± 45 ppt (n=12). System blanks contribute roughly half the amount of ethane extracted from a 300 g ice core sample. These preliminary data exhibit a temporal trend, with higher ethane levels from 0-900 C.E., followed by a decline, reaching a minimum between 1600-1700 C.E. These trends are consistent with variations in ice core methane isotopes and carbon monoxide isotopes (Ferretti et al., 2005, Wang et al., 2010), which indicate changes in biomass burning emissions over this time period. These preliminary data suggest that Antarctic ice core bubbles contain paleoatmospheric ethane levels. With further improvement of laboratory techniques it appears

Modeling CO, CO2, and H2O Ice Abundances in the Envelopes of Young Stellar Objects in the Magellanic Clouds

NASA Astrophysics Data System (ADS)

Pauly, Tyler; Garrod, Robin T.

2018-02-01

Massive young stellar objects (MYSOs) in the Magellanic Clouds show infrared absorption features corresponding to significant abundances of CO, CO2, and H2O ice along the line of sight, with the relative abundances of these ices differing between the Magellanic Clouds and the Milky Way. CO ice is not detected toward sources in the Small Magellanic Cloud, and upper limits put its relative abundance well below sources in the Large Magellanic Cloud and the Milky Way. We use our gas-grain chemical code MAGICKAL, with multiple grain sizes and grain temperatures, and further expand it with a treatment for increased interstellar radiation field intensity to model the elevated dust temperatures observed in the MCs. We also adjust the elemental abundances used in the chemical models, guided by observations of H II regions in these metal-poor satellite galaxies. With a grid of models, we are able to reproduce the relative ice fractions observed in MC MYSOs, indicating that metal depletion and elevated grain temperature are important drivers of the MYSO envelope ice composition. Magellanic Cloud elemental abundances have a subgalactic C/O ratio, increasing H2O ice abundances relative to the other ices; elevated grain temperatures favor CO2 production over H2O and CO. The observed shortfall in CO in the Small Magellanic Cloud can be explained by a combination of reduced carbon abundance and increased grain temperatures. The models indicate that a large variation in radiation field strength is required to match the range of observed LMC abundances. CH3OH abundance is found to be enhanced in low-metallicity models, providing seed material for complex organic molecule formation in the Magellanic Clouds.

Carbonyl sulfide during the late Holocene from measurements in Antarctic ice cores (Invited)

NASA Astrophysics Data System (ADS)

Aydin, M.; Fudge, T. J.; Verhulst, K. R.; Waddington, E. D.; Saltzman, E. S.

2013-12-01

Carbonyl sulfide (COS) is the most abundant sulfur gas in the troposphere with a global average mixing ratio of about 500 parts per trillion (ppt) and a lifetime of 3 years. It is produced by a variety of natural and anthropogenic sources. Oceans are the largest source, emitting COS and precursors carbon disulfide and dimethyl sulfide. The most important removal process of COS is uptake by terrestrial plants during photosynthesis. Interest in the atmospheric variability of COS is primarily due to its potential value as a proxy for changes in gross primary productivity of the land biosphere. Ice core COS records may provide the long term observational basis needed to explore climate driven changes in terrestrial productivity and the resulting impacts, for example, on atmospheric CO2 levels. Previous measurements in a South Pole ice core established the preindustrial COS levels at ~30% of the modern atmosphere and revealed that atmospheric COS increased at an average rate of 1.8 ppt per 100 years over the last 2,000 years [Aydin et al., 2008]. We have since measured COS in 5 additional ice cores from 4 different sites in Antarctica. These measurements display a site-dependent downcore decline in COS, apparently driven by in situ hydrolysis. The reaction is strongly temperature dependent, with the hydrolysis lifetimes (e-folding) ranging from thousands to hundreds of thousands of years. We implement a novel technique that uses ice and heat flow models to predict temperature histories for the ice core samples from different sites and correct for the COS lost to in situ hydrolysis assuming first order kinetics. The 'corrected' COS records confirm the trend observed previously in the COS record from the South Pole ice core. The new, longer record suggests the slow increase in atmospheric COS may have started about 5,000 years ago and continued for 4,500 years until levels stabilized about 500 years ago. Atmospheric CO2 was also rising during this time period, suggesting

Chemistry of microparticles trapped in last glacial period ice of EPICA-DML deep ice core

NASA Astrophysics Data System (ADS)

Nedelcu, Aneta F.; Faria, Sérgio H.; Kipfstuhl, Sepp; Kuhs, Werner F.

2010-05-01

The EDML ice core, drilled within the framework of the European project for Ice Coring in Antarctica, (EPICA), in the interior of Dronning Maud Land, DML, Antarctica (at 75°S, 0°E), is the first deep ice core in the Atlantic sector of the Southern Ocean region that provides higher-resolution atmosphere and climate records for the last glacial period, when compared with other ice cores retrieved from the East Antarctic plateau [1]. The chemical impurities embedded in the ice matrix of an ice sheet are basic proxies for climate reconstruction, and their concentration and composition usually determine the occurrence of distinct (cloudy or clear) strata in the ice sheet structure. The easiest observable impurities in polar ice are air bubbles. But a considerable amount of the impurities trapped inside ice layers are observed as microscopic deposits of solid (soluble or insoluble) particles, not bigger than a few micra in size, called microinclusions. Layers of ice with a high content of (micro)inclusions are in general called cloudy bands and are considered to have been formed from the precipitations deposited during colder periods. Roughly, we expect that the colder the climate during the time the snow accumulated, the cloudier the ice stratum that forms afterwards [2]. Mainly by means of in-situ micro-Raman spectroscopy, it has been shown that in Antarctic glacial ice the soluble microinclusions occur mostly as sulphate and nitrate salts [3], while in Arctic ice more commonly as carbonate salts [4]. These findings could be explained in terms of different aerosol compositions determined by the specific regional environments and climatic conditions [5]. Regarding the insoluble particles that might exist in natural ice, with higher frequency in ice layers formed during glacial type stages, the general findings classify them in the (alumino)silicate mineralogical class [6]. Microinclusions existent in solid samples taken from clear and cloudy ice layers, corresponding

The isotopic composition of methane in polar ice cores

NASA Technical Reports Server (NTRS)

Craig, H.; Chou, C. C.; Welhan, J. A.; Stevens, C. M.; Engelkemeir, A.

1988-01-01

Air bubbles in polar ice cores indicate that about 300 years ago the atmospheric mixing ratio of methane began to increase rapidly. Today the mixing ratio is about 1.7 parts per million by volume, and, having doubled once in the past several hundred years, it will double again in the next 60 years if current rates continue. Carbon isotope ratios in methane up to 350 years in age have been measured with as little as 25 kilograms of polar ice recovered in 4-meter-long ice-core segments. The data show that: (1) in situ microbiology or chemistry has not altered the ice-core methane concentrations, and (2) that the carbon-13 to carbon-12 ratio of atmospheric CH4 in ice from 100 years and 300 years ago was about 2 per mil lower than at present. Atmospheric methane has a rich spectrum of isotopic sources: the ice-core data indicate that anthropogenic burning of the earth's biomass is the principal cause of the recent C-13H4 enrichment, although other factors may also contribute.

Implications of high amplitude atmospheric CO2 fluctuations on past millennium climate change

NASA Astrophysics Data System (ADS)

van Hoof, Thomas; Kouwenberg, Lenny; Wagner-Cremer, Friederike; Visscher, Henk

2010-05-01

Stomatal frequency analysis of leaves of land plants preserved in peat and lake deposits can provide a proxy record of pre-industrial atmospheric CO2 concentration complementary to measurements in Antarctic ice cores. Stomatal frequency based CO2 trends from the USA and NW European support the presence of significant CO2 variability during the first half of the last millennium (Kouwenberg et al., 2005; Wagner et al., 2004; van Hoof et al., 2008). The timing of the most significant perturbation in the stomata records (1200 AD) is in agreement with an observed CO2 fluctuation in the D47 Antarctic ice-core record (Barnola et al., 1995; van Hoof et al., 2005). The amplitude of the stomatal frequency based CO2 changes (> 34ppmv) exceeds the maximum amplitude of CO2 variability in the D47 ice core (< 10 ppmv). A modelling experiment taking into account firn-densification based smoothing processes in the D47 ice core proved, however, that the amplitude difference between the stomata record and the D47 ice-core can be explained by natural smoothing processes in the ice (van Hoof et al., 2005). This observation gives credence to the existence of high-amplitude CO2 fluctuations during the last millennium and suggests that high resolution ice core CO2 records should be regarded as a smoothed representation of the atmospheric CO2 signal. In the present study, potential marine and terrestrial sources and sinks associated with the observed atmospheric CO2 perturbation will be discussed. The magnitude of the observed CO2 variability implies that inferred changes in CO2 radiative forcing are of a similar magnitude as variations ascribed to other forcing mechanisms (e.g. solar forcing and volcanism), therefore challenging the IPCC concept of CO2 as an insignificant preindustrial climate forcing factor. References Barnola J.M., M. Anklin, J. Porcheron, D. Raynaud, J. Schwander and B. Stauffer 1995. CO2 evolution during the last millennium as recorded by Antarctic and Greenland ice

Characterization of thin film CO2 ice through the infrared ν1 + ν3 combination mode

NASA Astrophysics Data System (ADS)

He, Jiao; Vidali, Gianfranco

2018-01-01

Carbon dioxide is abundant in ice mantles of dust grains; some is found in the pure crystalline form as inferred from the double peak splitting of the bending profile at about 650 cm-1. To study how CO2 segregates into the pure form from water-rich mixtures of ice mantles and how it then crystallizes, we used Reflection Absorption InfraRed Spectroscopy to study the structural change of pure CO2 ice as a function of both ice thickness and temperature. We found that the ν1 + ν3 combination mode absorption profile at 3708 cm-1 provides an excellent probe to quantify the degree of crystallinity in CO2 ice. We also found that between 20 and 30 K, there is an ordering transition that we attribute to reorientation of CO2 molecules, while the diffusion of CO2 becomes significant at much higher temperatures. In the formation of pure crystalline CO2 in interstellar medium ices, the rate limiting process is the diffusion/segregation of CO2 molecules in the ice instead of the phase transition from amorphous to crystalline after clusters/islands of CO2 are formed.

Synthesis and detection the oxidization of Co cores of Co@SiO2 core-shell nanoparticles by in situ XRD and EXAFS.

PubMed

Zhang, Kunhao; Zhao, Ziyan; Wu, Zhonghua; Zhou, Ying

2015-01-01

In this paper, the Co@SiO2 core-shell nanoparticles were prepared by the sol-gel method. The oxidization of Co core nanoparticles was studied by the synchrotron radiation-based techniques including in situ X-ray diffraction (XRD) and X-ray absorption fine structure (XAFS) up to 800°C in air and N2 protection conditions, respectively. It was found that the oxidization of Co cores is undergoing three steps regardless of being in air or in N2 protection condition. In the first step ranging from room temperature to 200°C, the Co cores were dominated by Co(0) state as well as small amount of Co(2+) ions. When temperature was above 300°C, the interface between Co cores and SiO2 shells was gradually oxidized into Co(2+), and the CoO layer was observed. As the temperature increasing to 800°C, the Co cores were oxidized to Co3O4 or Co3O4/CoO. Nevertheless, the oxidization kinetics of Co cores is different for the Co@SiO2 in air and N2 gas conditions. Generally, the O2 in the air could get through the SiO2 shells easily onto the Co core surface and induce the oxidization of the Co cores due to the mesoporous nature of the SiO2 shells. However, in N2 gas condition, the O atoms can only be from the SiO2 shells, so the diffusion effect of O atoms in the interface between Co core and SiO2 shell plays a key role.

Experimental evidence for carbonate precipitation and CO 2 degassing during sea ice formation

NASA Astrophysics Data System (ADS)

Papadimitriou, S.; Kennedy, H.; Kattner, G.; Dieckmann, G. S.; Thomas, D. N.

2004-04-01

Chemical and stable carbon isotopic modifications during the freezing of artificial seawater were measured in four 4 m 3 tank incubations. Three of the four incubations were inoculated with a nonaxenic Antarctic diatom culture. The 18 days of freezing resulted in 25 to 27 cm thick ice sheets overlying the residual seawater. The ice phase was characterized by a decrease in temperature from -1.9 to -2.2°C in the under-ice seawater down to -6.7°C in the upper 4 cm of the ice sheet, with a concurrent increase in the salinity of the under-ice seawater and brine inclusions of the ice sheet as a result of physical concentration of major dissolved salts by expulsion from the solid ice matrix. Measurements of pH, total dissolved inorganic carbon (C T) and its stable isotopic composition (δ 13C T) all exhibited changes, which suggest minimal effect by biological activity during the experiment. A systematic drop in pH and salinity-normalized C T by up to 0.37 pH SWS units and 376 μmol C kg -1 respectively at the lowest temperature and highest salinity part of the ice sheet were coupled with an equally systematic 13C enrichment of the C T. Calculations based on the direct pH and C T measurements indicated a steady increase in the in situ concentration of dissolved carbon dioxide (CO 2(aq)) with time and increasing salinity within the ice sheet, partly due to changes in the dissociation constants of carbonic acid in the low temperature-high salinity range within sea ice. The combined effects of temperature and salinity on the solubility of CO 2 over the range of conditions encountered during this study was a slight net decrease in the equilibrium CO 2(aq) concentration as a result of the salting-out overriding the increase in solubility with decreasing temperature. Hence, the increase in the in situ CO 2(aq) concentration lead to saturation or supersaturation of the brine inclusions in the ice sheet with respect to atmospheric pCO 2 (≈3.5 × 10 -4 atm). When all physico

Toward an integrated ice core chronology using relative and orbital tie-points

NASA Astrophysics Data System (ADS)

Bazin, L.; Landais, A.; Lemieux-Dudon, B.; Toyé Mahamadou Kele, H.; Blunier, T.; Capron, E.; Chappellaz, J.; Fischer, H.; Leuenberger, M.; Lipenkov, V.; Loutre, M.-F.; Martinerie, P.; Parrenin, F.; Prié, F.; Raynaud, D.; Veres, D.; Wolff, E.

2012-04-01

Precise ice cores chronologies are essential to better understand the mechanisms linking climate change to orbital and greenhouse gases concentration forcing. A tool for ice core dating (DATICE [developed by Lemieux-Dudon et al., 2010] permits to generate a common time-scale integrating relative and absolute dating constraints on different ice cores, using an inverse method. Nevertheless, this method has only been applied for a 4-ice cores scenario and for the 0-50 kyr time period. Here, we present the bases for an extension of this work back to 800 ka using (1) a compilation of published and new relative and orbital tie-points obtained from measurements of air trapped in ice cores and (2) an adaptation of the DATICE inputs to 5 ice cores for the last 800 ka. We first present new measurements of δ18Oatm and δO2/N2 on the Talos Dome and EPICA Dome C (EDC) ice cores with a particular focus on Marine Isotopic Stages (MIS) 5, and 11. Then, we show two tie-points compilations. The first one is based on new and published CH4 and δ18Oatm measurements on 5 ice cores (NorthGRIP, EPICA Dronning Maud Land, EDC, Talos Dome and Vostok) in order to produce a table of relative gas tie-points over the last 400 ka. The second one is based on new and published records of δO2/N2, δ18Oatm and air content to provide a table of orbital tie-points over the last 800 ka. Finally, we integrate the different dating constraints presented above in the DATICE tool adapted to 5 ice cores to cover the last 800 ka and show how these constraints compare with the established gas chronologies of each ice core.

FTIR study of CO2 and H2O/CO2 nanoparticles and their temporal evolution at 80 K.

PubMed

Taraschewski, M; Cammenga, H K; Tuckermann, R; Bauerecker, S

2005-04-21

Fourier transform infrared (FTIR) spectroscopy combined with a long-path collisional cooling cell was used to investigate the temporal evolution of CO2 nanoparticles and binary H2O/CO2 nanocomposites in the aerosol phase at 80 K. The experimental conditions for the formation of different CO2 particle shapes as slab, shell, sphere, cube, and needle have been studied by comparison with calculated data from the literature. The H2O/CO2 nanoparticles were generated with a newly developed multiple-pulse injection technique and with the simpler flow-in technique. The carbon dioxide nu3-vibration band at 2360 cm(-1) and the water ice OH-dangling band at 3700 cm(-1) were used to study the evolution of structure, shape, and contact area of the nanocomposites over 150 s. Different stages of binary nanocomposites with primary water ice cores were identified dependent on the injected CO2 portion: (a) disordered (amorphous) CO2 slabs on water particle surfaces, (b) globular crystalline CO2 humps sticking on the water cores, and (c) water cores being completely enclosed in bigger predominantly crystalline CO2 nanoparticles. However, regular CO2 shell structures on primary water particles showing both longitudinal (LO) and transverse (TO) optical mode features of the nu3-vibration band could not be observed. Experiments with reversed nucleation order indicate that H2O/CO2 composite particles with different initial structures evolve toward similar molecular nanocomposites with separated CO2 and H2O regions.

On the use of δ18Oatm for ice core dating

NASA Astrophysics Data System (ADS)

Extier, Thomas; Landais, Amaelle; Bréant, Camille; Prié, Frédéric; Bazin, Lucie; Dreyfus, Gabrielle; Roche, Didier M.; Leuenberger, Markus

2018-04-01

Deep ice core chronologies have been improved over the past years through the addition of new age constraints. However, dating methods are still associated with large uncertainties for ice cores from the East Antarctic plateau where layer counting is not possible. Indeed, an uncertainty up to 6 ka is associated with AICC2012 chronology of EPICA Dome C (EDC) ice core, which mostly arises from uncertainty on the delay between changes recorded in δ18Oatm and in June 21st insolation variations at 65°N used for ice core orbital dating. Consequently, we need to enhance the knowledge of this delay to improve ice core chronologies. We present new high-resolution EDC δ18Oatm record (153-374 ka) and δO2/N2 measurements (163-332 ka) performed on well-stored ice to provide continuous records of δ18Oatm and δO2/N2 between 100 and 800 ka. The comparison of δ18Oatm with the δ18Ocalcite from East Asian speleothems shows that both signals present similar orbital and millennial variabilities, which may represent shifts in the InterTropical Convergence Zone position, themselves associated with Heinrich events. We thus propose to use the δ18Ocalcite as target for δ18Oatm orbital dating. Such a tuning method improves the ice core chronology of the last glacial inception compared to AICC2012 by reconciling NGRIP and mid-latitude climatic records. It is especially marked during Dansgaard-Oeschger 25 where the proposed chronology is 2.2 ka older than AICC2012. This δ18Oatm - δ18Ocalcite alignment method applied between 100 and 640 ka improves the EDC ice core chronology, especially over MIS 11, and leads to lower ice age uncertainties compared to AICC2012.

The condensation and vaporization behavior of ices containing SO2, H2S, and CO2: Implications for Io

NASA Technical Reports Server (NTRS)

Sandford, Scott A.; Allamandola, Louis J.

1993-01-01

In an extension of previously reported work on ices containing CO, CO2, H2O, CH3OH, NH3, and H2, measurements of the physical and infrared spectral properties of ices containing molecules relevant to Jupiter's moon Io are presented. These include studies on ice systems containing SO2, H2S, and CO2. The condensation and sublimation behaviors of each ice system and surface binding energies of their components are discussed. The surface binding energies can be used to calculate the residence times of the molecules on a surface as a function of temperature and thus represent important parameters for any calculation that attempts to model the transport of these molecules on Io's surface. The derived values indicate that SO2 frosts on Io are likely to anneal rapidly, resulting in less fluffy, 'glassy' ices and that H2S can be trapped in the SO2 ices of Io during night-time hours provided that SO2 deposition rates are on the order of 5 micrometers/hr or larger.

Precession and atmospheric CO2 modulated variability of sea ice in the central Okhotsk Sea since 130,000 years ago

NASA Astrophysics Data System (ADS)

Lo, Li; Belt, Simon T.; Lattaud, Julie; Friedrich, Tobias; Zeeden, Christian; Schouten, Stefan; Smik, Lukas; Timmermann, Axel; Cabedo-Sanz, Patricia; Huang, Jyh-Jaan; Zhou, Liping; Ou, Tsong-Hua; Chang, Yuan-Pin; Wang, Liang-Chi; Chou, Yu-Min; Shen, Chuan-Chou; Chen, Min-Te; Wei, Kuo-Yen; Song, Sheng-Rong; Fang, Tien-Hsi; Gorbarenko, Sergey A.; Wang, Wei-Lung; Lee, Teh-Quei; Elderfield, Henry; Hodell, David A.

2018-04-01

Recent reduction in high-latitude sea ice extent demonstrates that sea ice is highly sensitive to external and internal radiative forcings. In order to better understand sea ice system responses to external orbital forcing and internal oscillations on orbital timescales, here we reconstruct changes in sea ice extent and summer sea surface temperature (SSST) over the past 130,000 yrs in the central Okhotsk Sea. We applied novel organic geochemical proxies of sea ice (IP25), SSST (TEX86L) and open water marine productivity (a tri-unsaturated highly branched isoprenoid and biogenic opal) to marine sediment core MD01-2414 (53°11.77‧N, 149°34.80‧E, water depth 1123 m). To complement the proxy data, we also carried out transient Earth system model simulations and sensitivity tests to identify contributions of different climatic forcing factors. Our results show that the central Okhotsk Sea was ice-free during Marine Isotope Stage (MIS) 5e and the early-mid Holocene, but experienced variable sea ice cover during MIS 2-4, consistent with intervals of relatively high and low SSST, respectively. Our data also show that the sea ice extent was governed by precession-dominated insolation changes during intervals of atmospheric CO2 concentrations ranging from 190 to 260 ppm. However, the proxy record and the model simulation data show that the central Okhotsk Sea was near ice-free regardless of insolation forcing throughout the penultimate interglacial, and during the Holocene, when atmospheric CO2 was above ∼260 ppm. Past sea ice conditions in the central Okhotsk Sea were therefore strongly modulated by both orbital-driven insolation and CO2-induced radiative forcing during the past glacial/interglacial cycle.

Cosmogenic 10Be Depth Profile in top 560 m of West Antarctic Ice Sheet Divide Ice Core

NASA Astrophysics Data System (ADS)

Welten, K. C.; Woodruff, T. E.; Caffee, M. W.; Edwards, R.; McConnell, J. R.; Bisiaux, M. M.; Nishiizumi, K.

2009-12-01

Concentrations of cosmogenic 10Be in polar ice samples are a function of variations in solar activity, geomagnetic field strength, atmospheric mixing and annual snow accumulation rates. The 10Be depth profile in ice cores also provides independent chronological markers to tie Antarctic to Greenland ice cores and to tie Holocene ice cores to the 14C dendrochronology record. We measured 10Be concentrations in 187 samples from depths of 0-560 m of the main WAIS Divide core, WDC06A. The ice samples are typically 1-2 kg and represent 2-4 m of ice, equivalent to an average temporal resolution of ~12 years, based on the preliminary age-depth scale proposed for the WDC core, (McConnell et al., in prep). Be, Al and Cl were separated using ion exchange chromatography techniques and the 10Be concentrations were measured by accelerator mass spectrometry (AMS) at PRIME lab. The 10Be concentrations range from 8.1 to 19.1 x 10^3 at/g, yielding an average of (13.1±2.1) x 10^3 at/g. Adopting an average snow accumulation rate of 20.9 cm weq/yr, as derived from the age-depth scale, this value corresponds to an average 10Be flux of (2.7±0.5) x 10^5 atoms/yr/cm2. This flux is similar to that of the Holocene part of the Siple Dome (Nishiizumi and Finkel, 2007) and Dome Fuji (Horiuchi et al. 2008) ice cores, but ~30% lower than the value of 4.0 x 10^5 atoms/yr/cm2 for GISP2 (Finkel and Nishiizumi, 1997). The periods of low solar activity, known as Oort, Wolf, Spörer, Maunder and Dalton minima, show ~20% higher 10Be concentrations/fluxes than the periods of average solar activity in the last millennium. The maximum 10Be fluxes during some of these periods of low solar activity are up to ~50% higher than average 10Be fluxes, as seen in other polar ice cores, which makes these peaks suitable as chronologic markers. We will compare the 10Be record in the WAIS Divide ice core with that in other Antarctic as well as Greenland ice cores and with the 14C treering record. Acknowledgment. This

Laboratory IR Studies and Astrophysical Implications of C2H2-Containing Binary Ices

NASA Technical Reports Server (NTRS)

Knez, C.; Moore, M.; Ferrante, R.; Hudson, R.

2012-01-01

Studies of molecular hot cores and protostellar environments have shown that the observed abundance of gas-phase acetylene (C2H2) cannot be matched by chemical models without the inclusion of C2H2 molecules subliming from icy grain mantles. Searches for infrared (IR) spectral features of solid-phase acetylene are under way, but few laboratory reference spectra of C2H2 in icy mixtures, which are needed for spectral fits to observational data, have been published. Here, we report a systematic study of the IR spectra of condensed-phase pure acetylene and acetylene in ices dominated by carbon monoxide (CO), carbon dioxide (CO2), methane (CH4), and water (H2O). We present new spectral data for these ices, including band positions and intrinsic band strengths. For each ice mixture and concentration, we also explore the dependence of acetylene's nu5-band position (743 cm-1, 13.46 micrometers) and FWHM on temperature. Our results show that the nu5 feature is much more cleanly resolved in ices dominated by non-polar and low-polarity molecules, specifically CO, CO2, and CH4, than in mixtures dominated by H2O-ice. We compare our laboratory ice spectra with observations of a quiescent region in Serpens.

The role of sea ice in 2 x CO2 climate model sensitivity. Part 1: The total influence of sea ice thickness and extent

NASA Technical Reports Server (NTRS)

Rind, D.; Healy, R.; Parkinson, C.; Martinson, D.

1995-01-01

As a first step in investigating the effects of sea ice changes on the climate sensitivity to doubled atmospheric CO2, the authors use a standard simple sea ice model while varying the sea ice distributions and thicknesses in the control run. Thinner ice amplifies the atmospheric temperature senstivity in these experiments by about 15% (to a warming of 4.8 C), because it is easier for the thinner ice to be removed as the climate warms. Thus, its impact on sensitivity is similar to that of greater sea ice extent in the control run, which provides more opportunity for sea ice reduction. An experiment with sea ice not allowed to change between the control and doubled CO2 simulations illustrates that the total effect of sea ice on surface air temperature changes, including cloud cover and water vapor feedbacks that arise in response to sea ice variations, amounts to 37% of the temperature sensitivity to the CO2 doubling, accounting for 1.56 C of the 4.17 C global warming. This is about four times larger than the sea ice impact when no feedbacks are allowed. The different experiments produce a range of results for southern high latitudes with the hydrologic budget over Antarctica implying sea level increases of varying magnitude or no change. These results highlight the importance of properly constraining the sea ice response to climate perturbations, necessitating the use of more realistic sea ice and ocean models.

FIRST INFRARED BAND STRENGTHS FOR AMORPHOUS CO{sub 2}, AN OVERLOOKED COMPONENT OF INTERSTELLAR ICES

DOE Office of Scientific and Technical Information (OSTI.GOV)

Gerakines, Perry A.; Hudson, Reggie L., E-mail: Reggie.Hudson@NASA.gov

2015-08-01

Solid carbon dioxide (CO{sub 2}) has long been recognized as a component of both interstellar and solar system ices, but a recent literature search has revealed significant qualitative and quantitative discrepancies in the laboratory spectra on which the abundances of extraterrestrial CO{sub 2} are based. Here we report new infrared (IR) spectra of amorphous CO{sub 2}-ice along with band intensities (band strengths) of four mid-IR absorptions, the first such results in the literature. A possible thickness dependence for amorphous-CO{sub 2} IR band shapes and positions also is investigated, and the three discordant reports of amorphous CO{sub 2} spectra in themore » literature are addressed. Applications of our results are discussed with an emphasis on laboratory investigations and results from astronomical observations. A careful comparison with earlier work shows that the IR spectra calculated from several databases for CO{sub 2} ices, all ices being made near 10 K, are not for amorphous CO{sub 2}, but rather for crystalline CO{sub 2} or crystalline-amorphous mixtures.« less

Systematic Variations in CO2/H2O Ice Abundance Ratios in Nearby Galaxies Found with AKARI Near-infrared Spectroscopy

NASA Astrophysics Data System (ADS)

Yamagishi, M.; Kaneda, H.; Ishihara, D.; Oyabu, S.; Onaka, T.; Shimonishi, T.; Suzuki, T.

2015-07-01

We report CO2/H2O ice abundance ratios in seven nearby star-forming galaxies based on the AKARI near-infrared (2.5-5.0 μm) spectra. The CO2/H2O ice abundance ratios show clear variations between 0.05 and 0.2 with the averaged value of 0.14 ± 0.01. The previous study on M82 revealed that the CO2/H2O ice abundance ratios strongly correlate with the intensity ratios of the hydrogen recombination Brα line to the polycyclic aromatic hydrocarbon (PAH) 3.3 μm feature. In the present study, however, we find no correlation for the seven galaxies as a whole due to systematic differences in the relation between CO2/H2O ice abundance and Brα/PAH 3.3 μm intensity ratios from galaxy to galaxy. This result suggests that there is another parameter that determines the CO2/H2O ice abundance ratios in a galaxy in addition to the Brα/PAH 3.3 μm ratios. We find that the CO2/H2O ice abundance ratios positively correlate with the specific star formation rates of the galaxies. From these results, we conclude that CO2/H2O ice abundance ratios tend to be high in young star-forming galaxies.

Structure, spectroscopy and dynamics of layered H2O and CO2 ices

USGS Publications Warehouse

,; Plattner, Nuria; Meuwly, Markus

2012-01-01

Molecular dynamics simulations of structural, spectroscopic and dynamical properties of mixed water–carbon dioxide (H2O–CO2) ices are discussed over temperature ranges relevant to atmospheric and astrophysical conditions. The simulations employ multipolar force fields to represent electrostatic interactions which are essential for spectroscopic and dynamical investigations. It is found that at the water/CO2 interface the water surface acts as a template for the CO2 component. The rotational reorientation times in both bulk phases agree well with experimental observations. A pronounced temperature effect on the CO2 reorientation time is observed between 100 K and 200 K. At the interface, water reorientation times are nearly twice as long compared to water in the bulk. The spectroscopy of such ices is rich in the far-infrared region of the spectrum and can be related to translational and rotational modes. Furthermore, spectroscopic signatures mediated across the water/CO2 interface are found in this frequency range (around 440 cm−1). These results will be particularly important for new airborne experiments such as planned for SOFIA.

The volume- and surface-binding energies of ice systems containing CO, CO2, and H2O

NASA Technical Reports Server (NTRS)

Sandford, Scott A.; Allamandola, Louis J.

1990-01-01

Laboratory-measured, temperature-dependent sticking efficiencies are presently used to derive the surface-binding energies of CO and CO2 on H2O-rich ices, with a view to determining the condensation and vaporization properties of these systems as well as to the measured energies' implications for both cometary behavior and the evolution of interstellar ices. The molecular volume and the surface binding energies are not found to be necessarily related on the basis of simple nearest-neighbor scaling in surface and bulk sites; this may be due to the physical constraints associated with matrix structure-associated physical constraints, which sometimes dominate the volume-binding energies.

Reconstructing the history of water ice formation from HDO/H2O and D2O/HDO ratios in protostellar cores

NASA Astrophysics Data System (ADS)

Furuya, K.; van Dishoeck, E. F.; Aikawa, Y.

2016-02-01

Recent interferometer observations have found that the D2O/HDO abundance ratio is higher than that of HDO/H2O by about one order of magnitude in the vicinity of low-mass protostar NGC 1333-IRAS 2A, where water ice has sublimated. Previous laboratory and theoretical studies show that the D2O/HDO ice ratio should be lower than the HDO/H2O ice ratio, if HDO and D2O ices are formed simultaneously with H2O ice. In this work, we propose that the observed feature, D2O/HDO > HDO/H2O, is a natural consequence of chemical evolution in the early cold stages of low-mass star formation as follows: 1) majority of oxygen is locked up in water ice and other molecules in molecular clouds, where water deuteration is not efficient; and 2) water ice formation continues with much reduced efficiency in cold prestellar/protostellar cores, where deuteration processes are highly enhanced as a result of the drop of the ortho-para ratio of H2, the weaker UV radiation field, etc. Using a simple analytical model and gas-ice astrochemical simulations, which traces the evolution from the formation of molecular clouds to protostellar cores, we show that the proposed scenario can quantitatively explain the observed HDO/H2O and D2O/HDO ratios. We also find that the majority of HDO and D2O ices are likely formed in cold prestellar/protostellar cores rather than in molecular clouds, where the majority of H2O ice is formed. This work demonstrates the power of the combination of the HDO/H2O and D2O/HDO ratios as a tool to reveal the past history of water ice formation in the early cold stages of star formation, and when the enrichment of deuterium in the bulk of water occurred. Further observations are needed to explore if the relation, D2O/HDO > HDO/H2O, is common in low-mass protostellar sources.

Rapid changes in ice core gas records - Part 1: On the accuracy of methane synchronisation of ice cores

NASA Astrophysics Data System (ADS)

Köhler, P.

2010-08-01

Methane synchronisation is a concept to align ice core records during rapid climate changes of the Dansgaard/Oeschger (D/O) events onto a common age scale. However, atmospheric gases are recorded in ice cores with a log-normal-shaped age distribution probability density function, whose exact shape depends mainly on the accumulation rate on the drilling site. This age distribution effectively shifts the mid-transition points of rapid changes in CH4 measured in situ in ice by about 58% of the width of the age distribution with respect to the atmospheric signal. A minimum dating uncertainty, or artefact, in the CH4 synchronisation is therefore embedded in the concept itself, which was not accounted for in previous error estimates. This synchronisation artefact between Greenland and Antarctic ice cores is for GRIP and Byrd less than 40 years, well within the dating uncertainty of CH4, and therefore does not calls the overall concept of the bipolar seesaw into question. However, if the EPICA Dome C ice core is aligned via CH4 to NGRIP this synchronisation artefact is in the most recent unified ice core age scale (Lemieux-Dudon et al., 2010) for LGM climate conditions of the order of three centuries and might need consideration in future gas chronologies.

First estimates of the contribution of CaCO3 precipitation to the release of CO2 to the atmosphere during young sea ice growth

NASA Astrophysics Data System (ADS)

Geilfus, N.-X.; Carnat, G.; Dieckmann, G. S.; Halden, N.; Nehrke, G.; Papakyriakou, T.; Tison, J.-L.; Delille, B.

2013-01-01

report measurements of pH, total alkalinity, air-ice CO2 fluxes (chamber method), and CaCO3 content of frost flowers (FF) and thin landfast sea ice. As the temperature decreases, concentration of solutes in the brine skim increases. Along this gradual concentration process, some salts reach their solubility threshold and start precipitating. The precipitation of ikaite (CaCO3.6H2O) was confirmed in the FF and throughout the ice by Raman spectroscopy and X-ray analysis. The amount of ikaite precipitated was estimated to be 25 µmol kg-1 melted FF, in the FF and is shown to decrease from 19 to 15 µmol kg-1 melted ice in the upper part and at the bottom of the ice, respectively. CO2 release due to precipitation of CaCO3 is estimated to be 50 µmol kg-1 melted samples. The dissolved inorganic carbon (DIC) normalized to a salinity of 10 exhibits significant depletion in the upper layer of the ice and in the FF. This DIC loss is estimated to be 2069 µmol kg-1 melted sample and corresponds to a CO2 release from the ice to the atmosphere ranging from 20 to 40 mmol m-2 d-1. This estimate is consistent with flux measurements of air-ice CO2 exchange. Our measurements confirm previous laboratory findings that growing young sea ice acts as a source of CO2 to the atmosphere. CaCO3 precipitation during early ice growth appears to promote the release of CO2 to the atmosphere; however, its contribution to the overall release by newly formed ice is most likely minor.

Sea ice and pollution-modulated changes in Greenland ice core methanesulfonate and bromine

NASA Astrophysics Data System (ADS)

Maselli, Olivia J.; Chellman, Nathan J.; Grieman, Mackenzie; Layman, Lawrence; McConnell, Joseph R.; Pasteris, Daniel; Rhodes, Rachael H.; Saltzman, Eric; Sigl, Michael

2017-01-01

Reconstruction of past changes in Arctic sea ice extent may be critical for understanding its future evolution. Methanesulfonate (MSA) and bromine concentrations preserved in ice cores have both been proposed as indicators of past sea ice conditions. In this study, two ice cores from central and north-eastern Greenland were analysed at sub-annual resolution for MSA (CH3SO3H) and bromine, covering the time period 1750-2010. We examine correlations between ice core MSA and the HadISST1 ICE sea ice dataset and consult back trajectories to infer the likely source regions. A strong correlation between the low-frequency MSA and bromine records during pre-industrial times indicates that both chemical species are likely linked to processes occurring on or near sea ice in the same source regions. The positive correlation between ice core MSA and bromine persists until the mid-20th century, when the acidity of Greenland ice begins to increase markedly due to increased fossil fuel emissions. After that time, MSA levels decrease as a result of declining sea ice extent but bromine levels increase. We consider several possible explanations and ultimately suggest that increased acidity, specifically nitric acid, of snow on sea ice stimulates the release of reactive Br from sea ice, resulting in increased transport and deposition on the Greenland ice sheet.

Recent Increases in Snow Accumulation and Decreases in Sea-Ice Concentration Recorded in a Coastal NW Greenland Ice Core

NASA Astrophysics Data System (ADS)

Osterberg, E. C.; Thompson, J. T.; Wong, G. J.; Hawley, R. L.; Kelly, M. A.; Lutz, E.; Howley, J.; Ferris, D. G.

2013-12-01

A significant rise in summer temperatures over the past several decades has led to widespread retreat of the Greenland Ice Sheet (GIS) margin and surrounding sea ice. Recent observations from geodetic stations and GRACE show that ice mass loss progressed from South Greenland up to Northwest Greenland by 2005 (Khan et al., 2010). Observations from meteorological stations at the U.S. Thule Air Force Base, remote sensing platforms, and climate reanalyses indicate a 3.5C mean annual warming in the Thule region and a 44% decrease in summer (JJAS) sea-ice concentrations in Baffin Bay from 1980-2010. Mean annual precipitation near Thule increased by 12% over this interval, with the majority of the increase occurring in fall (SON). To improve projections of future ice loss and sea-level rise in a warming climate, we are currently developing multi-proxy records (lake sediment cores, ice cores, glacial geologic data, glaciological models) of Holocene climate variability and cryospheric response in NW Greenland, with a focus on past warm periods. As part of our efforts to develop a millennial-length ice core paleoclimate record from the Thule region, we collected and analyzed snow pit samples and short firn cores (up to 20 m) from the coastal region of the GIS (2Barrel site; 76.9317 N, 63.1467 W) and the summit of North Ice Cap (76.938 N, 67.671 W) in 2011 and 2012, respectively. The 2Barrel ice core was sampled using a continuous ice core melting system at Dartmouth, and subsequently analyzed for major anion and trace element concentrations and stable water isotope ratios. Here we show that the 2Barrel ice core spanning 1990-2010 records a 25% increase in mean annual snow accumulation, and is positively correlated (r = 0.52, p<0.01) with ERA-Interim precipitation. The 2Barrel annual sea-salt Na concentration is strongly correlated (r = 0.5-0.8, p<0.05) with summer and fall sea-ice concentrations in northern Baffin Bay near Thule (Figure 1). We hypothesize that the positive

The evolution of pCO2, ice volume and climate during the middle Miocene

NASA Astrophysics Data System (ADS)

Foster, Gavin L.; Lear, Caroline H.; Rae, James W. B.

2012-08-01

The middle Miocene Climatic Optimum (17-15 Ma; MCO) is a period of global warmth and relatively high CO2 and is thought to be associated with a significant retreat of the Antarctic Ice Sheet (AIS). We present here a new planktic foraminiferal δ11B record from 16.6 to 11.8 Ma from two deep ocean sites currently in equilibrium with the atmosphere with respect to CO2. These new data demonstrate that the evolution of global climate during the middle Miocene (as reflected by changes in the cyrosphere) was well correlated to variations in the concentration of atmospheric CO2. What is more, within our sampling resolution (∼1 sample per 300 kyr) there is no evidence of hysteresis in the response of ice volume to CO2 forcing during the middle Miocene, contrary to what is understood about the Antarctic Ice Sheet from ice sheet modelling studies. In agreement with previous data, we show that absolute levels of CO2 during the MCO were relatively modest (350-400 ppm) and levels either side of the MCO are similar or lower than the pre-industrial (200-260 ppm). These new data imply the presence of either a very dynamic AIS at relatively low CO2 during the middle Miocene or the advance and retreat of significant northern hemisphere ice. Recent drilling on the Antarctic margin and shore based studies indicate significant retreat and advance beyond the modern limits of the AIS did occur during the middle Miocene, but the complete loss of the AIS was unlikely. Consequently, it seems that ice volume and climate variations during the middle Miocene probably involved a more dynamic AIS than the modern but also some component of land-based ice in the northern hemisphere.

Toward unified ice core chronologies with the DatIce tool

NASA Astrophysics Data System (ADS)

Toye Mahamadou Kele, H.; Lemieux-Dudon, B.; Blayo, E.

2012-04-01

Antarctic and Greenland ice cores provide a means to study the phase relationships of climate changes in both hemispheres. They also enable to study the timing between climate, and greenhouse gases or orbital forcings. One key step for such studies is to improve the absolute and relative precisions of ice core age scales (for ice and trapped gas), and beyond that, to try to reach the best consistency between chronologies of paleo records of any kind. The DatIce tool is designed to increase the consistency between pre-existing (also called background) core chronologies. It formulates a variational inverse problem which aims at correcting three key quantities that uniquely define the core age scales: the accumulation rate, the total thinning function, and the close-off depth. For that purpose, it integrates paleo data constraints of many types among which age markers (with for instance documented volcanoes eruptions), and stratigraphic links (with for instance abrupt changes in methane concentration). A cost function is built that enables to calculate new chronologies by making a trade-off between all the constraints (background chronologies and paleo data). The method presented in Lemieux-Dudon et al (2010) has already been applied simultaneously to EPICA EDML and EDC, Vostok and NGRIP. Currently, on going works are conducted at LSCE Saclay and LGGE Grenoble laboratories to construct unified Antarctic chronologies by applying the DatIce tool with new ice cores and new sets of paleo measurements. We here present the DatIce tool, the underlying methodology, and its potential applications. We further show some improvements that have been made recently. We especially adress the issue related to the calibration of the error of pre-existing core chronologies. They are inputs that may have a strong impact on the results. However these uncertainties are uneasy to analyze, since prior chronologies are most of the time assessed on the basis of glaciological models (firn

The Effect of CO2 Ice Cap Sublimation on Mars Atmosphere

NASA Technical Reports Server (NTRS)

Batterson, Courtney

2016-01-01

Sublimation of the polar CO2 ice caps on Mars is an ongoing phenomenon that may be contributing to secular climate change on Mars. The transfer of CO2 between the surface and atmosphere via sublimation and deposition may alter atmospheric mass such that net atmospheric mass is increasing despite seasonal variations in CO2 transfer. My study builds on previous studies by Kahre and Haberle that analyze and compare data from the Phoenix and Viking Landers 1 and 2 to determine whether secular climate change is happening on Mars. In this project, I use two years worth of temperature, pressure, and elevation data from the MSL Curiosity rover to create a program that allows for successful comparison of Curiosity pressure data to Viking Lander pressure data so a conclusion can be drawn regarding whether CO2 ice cap sublimation is causing a net increase in atmospheric mass and is thus contributing to secular climate change on Mars.

An Improved Extraction and Analysis Technique for Determination of Carbon Monoxide Stable Isotopes and Mixing Ratios from Ice Core and Atmospheric Air Samples.

NASA Astrophysics Data System (ADS)

Place, P., Jr.; Petrenko, V. V.; Vimont, I.

2017-12-01

Carbon Monoxide (CO) is an important atmospheric trace gas that affects the oxidative capacity of the atmosphere and contributes indirectly to anthropogenic radiative forcing. Carbon monoxide stable isotopes can also serve as a tracer for variations in biomass burning, particularly in the preindustrial atmosphere. A good understanding of the past variations in CO mole fractions and isotopic composition can help improve the skill of chemical transport models and constrain biomass burning changes. Ice cores may preserve a record of past atmospheric CO for analysis and interpretation. To this end, a new extraction system has been developed for analysis of stable isotopes (δ13CO and δC18O) of atmospheric carbon monoxide from ice core and atmospheric air samples. This system has been designed to measure relatively small sample sizes (80 cc STP of air) to accommodate the limited availability of ice core samples. Trapped air is extracted from ice core samples via melting in a glass vacuum chamber. This air is expanded into a glass expansion loop and then compressed into the sample loop of a Reducing Gas Detector (Peak Laboratories, Peak Performer 1 RCP) for the CO mole fraction measurement. The remaining sample gas will be expelled from the melt vessel into a larger expansion loop via headspace compression for isotopic analysis. The headspace compression will be accomplished by introduction of clean degassed water into the bottom of the melt vessel. Isotopic analysis of the sample gas is done utilizing the Schütze Reagent to convert the carbon monoxide to carbon dioxide (CO2) which is then measured using continuous-flow isotope ratio mass spectrometry (Elementar Americas, IsoPrime 100). A series of cryogenic traps are used to purify the sample air, capture the converted sample CO2, and cryofocus the sample CO2 prior to injection.

Atmospheric CO2 and abrupt climate change on submillennial timescales

NASA Astrophysics Data System (ADS)

Ahn, Jinho; Brook, Edward

2010-05-01

How atmospheric CO2 varies and is controlled on various time scales and under various boundary conditions is important for understanding how the carbon cycle and climate change are linked. Ancient air preserved in ice cores provides important information on past variations in atmospheric CO2. In particular, concentration records for intervals of abrupt climate change may improve understanding of mechanisms that govern atmospheric CO2. We present new multi-decadal CO2 records that cover Greenland stadial 9 (between Dansgaard-Oeschger (DO) events 8 and 9) and the abrupt cooling event at 8.2 ka. The CO2 records come from Antarctic ice cores but are well synchronized with Greenland ice core records using new high-resolution CH4 records,precisely defining the timing of CO2 change with respect to abrupt climate events in Greenland. Previous work showed that during stadial 9 (40~38 ka), CO2 rose by about 15~20 ppm over around 2,000 years, and at the same time temperatures in Antarctica increased. Dust proxies indicate a decrease in dust flux over the same period. With more detailed data and better age controls we now find that approximately half of the CO2 increase during stadial 9 occurred abruptly, over the course of decades to a century at ~39.6 ka. The step increase of CO2 is synchronous with a similar step increase of Antarctic isotopic temperature and a small abrupt change in CH4, and lags after the onset of decrease in dust flux by ~400 years. New atmospheric CO2 records at the well-known ~8.2 ka cooling event were obtained from Siple Dome ice core, Antarctica. Our preliminary CO2 data span 900 years and include 19 data points within the 8.2 ka cooling event, which persisted for ~160 years (Thomas et al., Quarternary Sci. Rev., 2007). We find that CO2 increased by 2~4 ppm during that cooling event. Further analyses will improve the resolution and better constrain the CO2 variability during other times in the early Holocene to determine if the variations observed

Marine Isotope Stage 11 : The Role of Co2, Insolation and Antarctica Ice Sheet On This Interglacial

NASA Astrophysics Data System (ADS)

Raynaud, D.; Loutre, M. F.; Ritz, C.; Barnola, J.-M.; Berger, A.; Chappellaz, J.; Jouzel, J.; Lipenkov, V.; Petit, J.-R.; Vimeux, F.

The Marine Isotopic Stage 11 (MIS 11), around 400kyr BP ago, has been suggested as an analogue for a future climate under natural forcing because of the similar condi- tions of orbitally driven insolation during this interglacial period and the one covering the Holocene and the near future. There are many open questions about unusual MIS 11 climatic conditions (length of the interglacial, temperature, sea level, marine car- bonate system), as recorded in different marine and continental records. The Antarctic Vostok ice core provides the only atmospheric record extending back to MIS 11 and we use it to discuss the Antarctic temperature, the atmospheric CO2 concentration and the ice sheet stability in the central part of East Antarctica during this interglacial. The unique nature of the Vostok atmospheric record leads us to use the available Vos- tok data to drive climate and ice sheet models for MIS 11. A model of intermediate complexity (LLN-2D model) is used to investigate the sensitivity of the simulated MIS 11 deglaciation to the interplay between insolation and CO2. It is shown that the length of the simulated interglacial depends strongly on the phasing between these two climate forcings. We also investigate the response of the Antarctic Ice Sheet to changing climate through simulations performed with the LGGE 3-D ice sheet model. The results indicate that sea level stands during MIS 11 as high as 20 m. above present level, as suggested by different elevated marine terraces, cannot be explained, except by assuming that MIS 11 was very dry over Antarctica.

14CO in Antarctic Glacial Ice as a Tracer of Changes in Atmospheric OH Abundance from 1880 AD to Present

NASA Astrophysics Data System (ADS)

Neff, P. D.; Petrenko, V. V.; Hmiel, B.; Smith, A. W.; Buizert, C.; Etheridge, D. M.; Murray, L. T.; Dyonisius, M.

2017-12-01

OH is the main tropospheric oxidant and determines the lifetime of methane and most other trace gases in the atmosphere, thereby controlling the amount of greenhouse warming that these gases can produce. Changes in [OH] in response to large changes in reactive trace gas emissions (which may occur in the future) are uncertain. Measurements of 14C-containing carbon monoxide (14CO) and other tracers such as methyl chloroform over the last ≈25 years have been successfully used to monitor changes in average OH concentration ([OH]), but there are no observational constraints on [OH] further back in time. Reconstructions of 14CO from ice cores could in principle provide such constraints but are complicated by in-situ production of 14CO by cosmic rays directly in the ice. Recent work in Antarctica and Greenland shows that this in-situ component would be relatively small and can be accurately corrected for at sites with very high snow accumulation rates. We propose to sample firn-air and shallow ice to ≈230 m depth at Law Dome, Antarctica (site DE-08, 1.2 m a-1 ice-equivalent snow accumulation), extracting trapped air from the ice cores on-site using a new large-volume ice melting system. 14CO will be analyzed in firn and ice core air samples, and accurate corrections made for the in-situ cosmogenic 14CO component in the ice—allowing for the atmospheric 14CO history to be reconstructed. This 14CO history will be interpreted with the aid of a chemistry-transport model to place the first observational constraints on the variability of Southern Hemisphere [OH] since ≈1880 AD.

Complex Coacervate Core Micelles Containing Poly(vinyl alcohol) Inhibit Ice Recrystallization.

PubMed

Sproncken, Christian C M; Surís-Valls, Romà; Cingil, Hande E; Detrembleur, Christophe; Voets, Ilja K

2018-04-10

Complex coacervate core micelles (C3Ms) form upon complexation of oppositely charged copolymers. These co-assembled structures are widely investigated as promising building blocks for encapsulation, nanoparticle synthesis, multimodal imaging, and coating technology. Here, the impact on ice growth is investigated of C3Ms containing poly(vinyl alcohol), PVA, which is well known for its high ice recrystallization inhibition (IRI) activity. The PVA-based C3Ms are prepared upon co-assembly of poly(4-vinyl-N-methyl-pyridinium iodide) and poly(vinyl alcohol)-block-poly(acrylic acid). Their formation conditions, size, and performance as ice recrystallization inhibitors are studied. It is found that the C3Ms exhibit IRI activity at PVA monomer concentrations as low as 1 × 10 -3 m. The IRI efficacy of PVA-C3Ms is similar to that of linear PVA and PVA graft polymers, underlining the influence of vinyl alcohol monomer concentration rather than polymer architecture. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Microshear in the deep EDML ice core analyzed using cryogenic EBSD

NASA Astrophysics Data System (ADS)

Kuiper, Ernst-Jan; Pennock, Gill; Drury, Martyn; Kipfstuhl, Sepp; Faria, Sérgio; Weikusat, Ilka

2017-04-01

Ice sheets play an important role in sea level evolution by storing large amounts of fresh water on land. The ice in an ice sheet flows from the interior of the ice sheet to the edges where it either melts or calves into the ocean. This flow of ice results from internal deformation of the ice aggregate. Dislocation creep is assumed to be the dominant deformation mechanism for polar ice and is grain size insensitive. Recently, a different deformation mechanism was identified in the deeper part of the EDML ice core (Antarctica) where, at a depth of 2385 meters, the grain size strongly decreases, the grain aspect ratio increase and, the inclination of the grain elongation changes (Faria et al., 2006; Weikusat et al., 2017). At this depth the borehole displacement increases strongly (Weikusat et al., 2017), which indicates a relatively high strain rate. Part of this EDML ice core section was studied using cryogenic electron backscattered diffraction (cryo-EBSD) (Weikusat et al, 2011). EBSD produces high resolution, full crystallographic (a-axis and c-axis) maps of the ice core samples. EBSD samples were taken from an ice core section at 2392.2 meter depth. This section was chosen for its very small grain size and the strongly aligned grain boundaries. The EBSD maps show a very low orientation gradient of <0.3° per millimetre inside the grains, which is 5-10 times lower than the orientation gradients found in other parts of the ice core. Furthermore, close to some grain boundaries, a relatively strong orientation gradient of 1°-2° per millimetre was found. The subgrain boundaries developed such that they elongate the sliding boundaries in order to accommodate the incompatibilities and maintain the strongly aligned grain boundary network. We identify the dominant deformation mechanism in this part of the ice core as grain boundary sliding accommodated by localized dislocation creep, which is a process similar to microshear (Drury and Humpreys, 1988). The existence of

Laboratory Spectra of CO2 Vibrational Modes in Planetary Ice Analogs

NASA Technical Reports Server (NTRS)

White, Douglas; Mastrapa, Rachel M.; Sandford, Scott

2012-01-01

Laboratory spectra have shown that CO2 is a powerful diagnostic tool for analyzing infrared data from remote observations, as it has been detected on icy moons in the outer Solar System as well as dust grain surfaces in the interstellar medium (ISM). IR absorption band profiles of CO2 within ice mixtures containing H2O and CH3OH change with respect to temperature and mixture ratios. In this particular study, the CO2 asymmetric stretching mode near 4.3 m (2350 cm (exp-1)), overtone mode near 1.97 m (5080 cm (exp-1)), and the combination bands near 2.7 m (3700 cm (exp-1)), 2.8 m (3600 cm (exp-1)), and 2.02 m (4960 cm (exp -1)), are systematically observed in different mixtures with H2O and CH3OH in temperature ranges from 15K to 150 K. Additionally, some high-temperature deposits (T greater than 50 K) of H2O, CH3OH, and CO2 ice mixtures were performed. These data may then be used to interpret infrared observational data obtained from icy surfaces in the outer Solar System and beyond.

Dansgaard-Oeschger cycles observed in the Greenland ReCAP ice core project

NASA Astrophysics Data System (ADS)

Kjær, Helle Astrid; Vallelonga, Paul; Vinther, Bo; Simonsen, Marius; Maffezzoli, Niccoló; Gkinis, Vasileios; Svensson, Anders; Jensen, Camilla Marie; Dallmayr, Remi; Spolaor, Andrea; Edwards, Ross

2017-04-01

The new REnland ice CAP (RECAP) ice core was drilled in summer 2015 in Greenland and measured by means of Continuous flow analysis (CFA) during the last 3 months of 2015. The Renland ice core was obtained as part of the ReCAP project, extending 584.11 meters to the bottom of the Renland ice cap located in east Greenland. The unique position on a mountain saddle above 2000 meters altitude, but close to the coast, ensures that the Renland ice core offers high accumulation, but also reaches far back in time. Results show that despite the short length the RECAP ice core holds ice all the way back to the past warm interglacial period, the Eemian. The glacial section is strongly thinned and covers on 20 meters of the ReCAP core, but nonetheless due to the high resolution of the measurements all 25 expected DO events could be identified. The record was analyzed for multiple elements including the water isotopes, forest fire tracers NH4+ and black carbon, insoluble dust particles by means of Abakus laser particle counter and the dust ion Ca2+, sea salt Na+, and sea ice proxies as well as acidity useful for finding volcanic layers to date the core. Below the glacial section another 20 meters of warm Eemian ice have been analysed. Here we present the chemistry results as obtained by continuous flow analysis (CFA) and compare the glacial section with the chemistry profile from other Greenland ice cores.

Optical properties of CO2 ice and CO2 snow from ultraviolet to infrared: Application to frost deposits and clouds on Mars

NASA Technical Reports Server (NTRS)

Hansen, Gary B.; Warren, Stephen G.; Leovy, Conway B.

1991-01-01

Researchers found that it is possible to grow large clear samples of CO2 ice at Mars-like temperatures of 150-170K if a temperature controlled refrigerator is connected to an isolated two-phase pure CO2 system. They designed a chamber for transmission measurements whose optical path between the 13mm diameter window is adjustable from 1.6mm to 107mm. This will allow measurements of linear absorption down to less than 0.01 cm (exp -1). A preliminary transmission spectrum of a thick sample of CO2 ice in the near infrared was obtained. Once revised optical constants have been determined as a function of wavelength and temperature, they can be applied to spectral reflectance/emissivity models for CO2 snow surfaces, both pure and contaminated with dust and water ice, using previously established approaches. It will be useful, also, to develop an infrared scattering-emission cloud radiance model (especially as viewed from near the limb) in order to develop a strategy for the identification of CO2 cloud layers by the atmospheric infrared radiometer instrument on the Mars Observer.

Ikaite crystal distribution in winter sea ice and implications for CO2 system dynamics

NASA Astrophysics Data System (ADS)

Rysgaard, S.; Søgaard, D. H.; Cooper, M.; Pućko, M.; Lennert, K.; Papakyriakou, T. N.; Wang, F.; Geilfus, N. X.; Glud, R. N.; Ehn, J.; McGinnis, D. F.; Attard, K.; Sievers, J.; Deming, J. W.; Barber, D.

2013-04-01

The precipitation of ikaite (CaCO3 ⋅ 6H2O) in polar sea ice is critical to the efficiency of the sea ice-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the ice is poorly known. We report unique observations of ikaite in unmelted ice and vertical profiles of ikaite abundance and concentration in sea ice for the crucial season of winter. Ice was examined from two locations: a 1 m thick land-fast ice site and a 0.3 m thick polynya site, both in the Young Sound area (74° N, 20° W) of NE Greenland. Ikaite crystals, ranging in size from a few μm to 700 μm, were observed to concentrate in the interstices between the ice platelets in both granular and columnar sea ice. In vertical sea ice profiles from both locations, ikaite concentration determined from image analysis, decreased with depth from surface-ice values of 700-900 μmol kg-1 ice (~25 × 106 crystals kg-1) to values of 100-200 μmol kg-1 ice (1-7 × 106 crystals kg-1) near the sea ice-water interface, all of which are much higher (4-10 times) than those reported in the few previous studies. Direct measurements of total alkalinity (TA) in surface layers fell within the same range as ikaite concentration, whereas TA concentrations in the lower half of the sea ice were twice as high. This depth-related discrepancy suggests interior ice processes where ikaite crystals form in surface sea ice layers and partly dissolve in layers below. Melting of sea ice and dissolution of observed concentrations of ikaite would result in meltwater with a pCO2 of <15 μatm. This value is far below atmospheric values of 390 μatm and surface water concentrations of 315 μatm. Hence, the meltwater increases the potential for seawater uptake of CO2.

SYSTEMATIC VARIATIONS IN CO{sub 2}/H{sub 2}O ICE ABUNDANCE RATIOS IN NEARBY GALAXIES FOUND WITH AKARI NEAR-INFRARED SPECTROSCOPY

DOE Office of Scientific and Technical Information (OSTI.GOV)

Yamagishi, M.; Kaneda, H.; Ishihara, D.

2015-07-01

We report CO{sub 2}/H{sub 2}O ice abundance ratios in seven nearby star-forming galaxies based on the AKARI near-infrared (2.5–5.0 μm) spectra. The CO{sub 2}/H{sub 2}O ice abundance ratios show clear variations between 0.05 and 0.2 with the averaged value of 0.14 ± 0.01. The previous study on M82 revealed that the CO{sub 2}/H{sub 2}O ice abundance ratios strongly correlate with the intensity ratios of the hydrogen recombination Brα line to the polycyclic aromatic hydrocarbon (PAH) 3.3 μm feature. In the present study, however, we find no correlation for the seven galaxies as a whole due to systematic differences in themore » relation between CO{sub 2}/H{sub 2}O ice abundance and Brα/PAH 3.3 μm intensity ratios from galaxy to galaxy. This result suggests that there is another parameter that determines the CO{sub 2}/H{sub 2}O ice abundance ratios in a galaxy in addition to the Brα/PAH 3.3 μm ratios. We find that the CO{sub 2}/H{sub 2}O ice abundance ratios positively correlate with the specific star formation rates of the galaxies. From these results, we conclude that CO{sub 2}/H{sub 2}O ice abundance ratios tend to be high in young star-forming galaxies.« less

The impact of dissolved organic carbon and bacterial respiration on pCO2 in experimental sea ice

NASA Astrophysics Data System (ADS)

Zhou, J.; Kotovitch, M.; Kaartokallio, H.; Moreau, S.; Tison, J.-L.; Kattner, G.; Dieckmann, G.; Thomas, D. N.; Delille, B.

2016-02-01

Previous observations have shown that the partial pressure of carbon dioxide (pCO2) in sea ice brines is generally higher in Arctic sea ice compared to those from the Antarctic sea ice, especially in winter and early spring. We hypothesized that these differences result from the higher dissolved organic carbon (DOC) content in Arctic seawater: Higher concentrations of DOC in seawater would be reflected in a greater DOC incorporation into sea ice, enhancing bacterial respiration, which in turn would increase the pCO2 in the ice. To verify this hypothesis, we performed an experiment using two series of mesocosms: one was filled with seawater (SW) and the other one with seawater with an addition of filtered humic-rich river water (SWR). The addition of river water increased the DOC concentration of the water from a median of 142 μmol Lwater-1 in SW to 249 μmol Lwater-1 in SWR. Sea ice was grown in these mesocosms under the same physical conditions over 19 days. Microalgae and protists were absent, and only bacterial activity has been detected. We measured the DOC concentration, bacterial respiration, total alkalinity and pCO2 in sea ice and the underlying seawater, and we calculated the changes in dissolved inorganic carbon (DIC) in both media. We found that bacterial respiration in ice was higher in SWR: median bacterial respiration was 25 nmol C Lice-1 h-1 compared to 10 nmol C Lice-1 h-1 in SW. pCO2 in ice was also higher in SWR with a median of 430 ppm compared to 356 ppm in SW. However, the differences in pCO2 were larger within the ice interiors than at the surfaces or the bottom layers of the ice, where exchanges at the air-ice and ice-water interfaces might have reduced the differences. In addition, we used a model to simulate the differences of pCO2 and DIC based on bacterial respiration. The model simulations support the experimental findings and further suggest that bacterial growth efficiency in the ice might approach 0.15 and 0.2. It is thus credible

The design and performance of IceCube DeepCore

NASA Astrophysics Data System (ADS)

Abbasi, R.; Abdou, Y.; Abu-Zayyad, T.; Ackermann, M.; Adams, J.; Aguilar, J. A.; Ahlers, M.; Allen, M. M.; Altmann, D.; Andeen, K.; Auffenberg, J.; Bai, X.; Baker, M.; Barwick, S. W.; Bay, R.; Bazo Alba, J. L.; Beattie, K.; Beatty, J. J.; Bechet, S.; Becker, J. K.; Becker, K.-H.; Benabderrahmane, M. L.; BenZvi, S.; Berdermann, J.; Berghaus, P.; Berley, D.; Bernardini, E.; Bertrand, D.; Besson, D. Z.; Bindig, D.; Bissok, M.; Blaufuss, E.; Blumenthal, J.; Boersma, D. J.; Bohm, C.; Bose, D.; Böser, S.; Botner, O.; Brown, A. M.; Buitink, S.; Caballero-Mora, K. S.; Carson, M.; Chirkin, D.; Christy, B.; Clevermann, F.; Cohen, S.; Colnard, C.; Cowen, D. F.; Cruz Silva, A. H.; D'Agostino, M. V.; Danninger, M.; Daughhetee, J.; Davis, J. C.; De Clercq, C.; Degner, T.; Demirörs, L.; Descamps, F.; Desiati, P.; de Vries-Uiterweerd, G.; DeYoung, T.; Díaz-Vélez, J. C.; Dierckxsens, M.; Dreyer, J.; Dumm, J. P.; Dunkman, M.; Eisch, J.; Ellsworth, R. W.; Engdegård, O.; Euler, S.; Evenson, P. A.; Fadiran, O.; Fazely, A. R.; Fedynitch, A.; Feintzeig, J.; Feusels, T.; Filimonov, K.; Finley, C.; Fischer-Wasels, T.; Fox, B. D.; Franckowiak, A.; Franke, R.; Gaisser, T. K.; Gallagher, J.; Gerhardt, L.; Gladstone, L.; Glüsenkamp, T.; Goldschmidt, A.; Goodman, J. A.; Góra, D.; Grant, D.; Griesel, T.; Groß, A.; Grullon, S.; Gurtner, M.; Ha, C.; Haj Ismail, A.; Hallgren, A.; Halzen, F.; Han, K.; Hanson, K.; Heinen, D.; Helbing, K.; Hellauer, R.; Hickford, S.; Hill, G. C.; Hoffman, K. D.; Hoffmann, B.; Homeier, A.; Hoshina, K.; Huelsnitz, W.; Hülß, J.-P.; Hulth, P. O.; Hultqvist, K.; Hussain, S.; Ishihara, A.; Jacobi, E.; Jacobsen, J.; Japaridze, G. S.; Johansson, H.; Kampert, K.-H.; Kappes, A.; Karg, T.; Karle, A.; Kenny, P.; Kiryluk, J.; Kislat, F.; Klein, S. R.; Köhne, J.-H.; Kohnen, G.; Kolanoski, H.; Köpke, L.; Koskinen, D. J.; Kowalski, M.; Kowarik, T.; Krasberg, M.; Kroll, G.; Kurahashi, N.; Kuwabara, T.; Labare, M.; Laihem, K.; Landsman, H.; Larson, M. J.; Lauer, R.; Lünemann, J.; Madsen, J.; Marotta, A.; Maruyama, R.; Mase, K.; Matis, H. S.; Meagher, K.; Merck, M.; Mészáros, P.; Meures, T.; Miarecki, S.; Middell, E.; Milke, N.; Miller, J.; Montaruli, T.; Morse, R.; Movit, S. M.; Nahnhauer, R.; Nam, J. W.; Naumann, U.; Nygren, D. R.; Odrowski, S.; Olivas, A.; Olivo, M.; O'Murchadha, A.; Panknin, S.; Paul, L.; Pérez de los Heros, C.; Petrovic, J.; Piegsa, A.; Pieloth, D.; Porrata, R.; Posselt, J.; Price, P. B.; Przybylski, G. T.; Rawlins, K.; Redl, P.; Resconi, E.; Rhode, W.; Ribordy, M.; Richman, M.; Rodrigues, J. P.; Rothmaier, F.; Rott, C.; Ruhe, T.; Rutledge, D.; Ruzybayev, B.; Ryckbosch, D.; Sander, H.-G.; Santander, M.; Sarkar, S.; Schatto, K.; Schmidt, T.; Schönwald, A.; Schukraft, A.; Schultes, A.; Schulz, O.; Schunck, M.; Seckel, D.; Semburg, B.; Seo, S. H.; Sestayo, Y.; Seunarine, S.; Silvestri, A.; Spiczak, G. M.; Spiering, C.; Stamatikos, M.; Stanev, T.; Stezelberger, T.; Stokstad, R. G.; Stößl, A.; Strahler, E. A.; Ström, R.; Stüer, M.; Sullivan, G. W.; Swillens, Q.; Taavola, H.; Taboada, I.; Tamburro, A.; Tepe, A.; Ter-Antonyan, S.; Tilav, S.; Toale, P. A.; Toscano, S.; Tosi, D.; van Eijndhoven, N.; Vandenbroucke, J.; Van Overloop, A.; van Santen, J.; Vehring, M.; Voge, M.; Walck, C.; Waldenmaier, T.; Wallraff, M.; Walter, M.; Weaver, Ch.; Wendt, C.; Westerhoff, S.; Whitehorn, N.; Wiebe, K.; Wiebusch, C. H.; Williams, D. R.; Wischnewski, R.; Wissing, H.; Wolf, M.; Wood, T. R.; Woschnagg, K.; Xu, C.; Xu, D. L.; Xu, X. W.; Yanez, J. P.; Yodh, G.; Yoshida, S.; Zarzhitsky, P.; Zoll, M.

2012-05-01

The IceCube neutrino observatory in operation at the South Pole, Antarctica, comprises three distinct components: a large buried array for ultrahigh energy neutrino detection, a surface air shower array, and a new buried component called DeepCore. DeepCore was designed to lower the IceCube neutrino energy threshold by over an order of magnitude, to energies as low as about 10 GeV. DeepCore is situated primarily 2100 m below the surface of the icecap at the South Pole, at the bottom center of the existing IceCube array, and began taking physics data in May 2010. Its location takes advantage of the exceptionally clear ice at those depths and allows it to use the surrounding IceCube detector as a highly efficient active veto against the principal background of downward-going muons produced in cosmic-ray air showers. DeepCore has a module density roughly five times higher than that of the standard IceCube array, and uses photomultiplier tubes with a new photocathode featuring a quantum efficiency about 35% higher than standard IceCube PMTs. Taken together, these features of DeepCore will increase IceCube's sensitivity to neutrinos from WIMP dark matter annihilations, atmospheric neutrino oscillations, galactic supernova neutrinos, and point sources of neutrinos in the northern and southern skies. In this paper we describe the design and initial performance of DeepCore.

The Design and Performance of IceCube DeepCore

NASA Technical Reports Server (NTRS)

Stamatikos, M.

2012-01-01

The IceCube neutrino observatory in operation at the South Pole, Antarctica, comprises three distinct components: a large buried array for ultrahigh energy neutrino detection, a surface air shower array, and a new buried component called DeepCore. DeepCore was designed to lower the IceCube neutrino energy threshold by over an order of magnitude, to energies as low as about 10 GeV. DeepCore is situated primarily 2100 m below the surface of the icecap at the South Pole, at the bottom center of the existing IceCube array, and began taking pbysics data in May 2010. Its location takes advantage of the exceptionally clear ice at those depths and allows it to use the surrounding IceCube detector as a highly efficient active veto against the principal background of downward-going muons produced in cosmic-ray air showers. DeepCore has a module density roughly five times higher than that of the standard IceCube array, and uses photomultiplier tubes with a new photocathode featuring a quantum efficiency about 35% higher than standard IceCube PMTs. Taken together, these features of DeepCore will increase IceCube's sensitivity to neutrinos from WIMP dark matter annihilations, atmospheric neutrino oscillations, galactic supernova neutrinos, and point sources of neutrinos in the northern and southern skies. In this paper we describe the design and initial performance of DeepCore.

Modelling the effects of ice-sheet activity on CO2 outgassing by Icelandic volcanoes

NASA Astrophysics Data System (ADS)

Armitage, J. J.; Ferguson, D.; Petersen, K. D.; Creyts, T. T.

2017-12-01

Glacial cycles may play a significant role in mediating the flux of magmatic CO2 between the Earth's mantle and atmosphere. In Iceland, it is thought that late-Pleistocene deglaciation led to a significant volcanic pulse, evidenced by increased post-glacial lava volumes and changes in melt chemistry consistent with depressurization. Investigating the extent to which glacial activity may have affected volcanic CO2 emissions from Iceland, and crucially over what timescale, requires detailed knowledge of how the magma system responded to the growth and collapse of the ice-sheet before and after the LGM. To investigate this, we coupled a model of magma generation and transport with a history of ice-sheet activity. Our results show that the emplacement and removal of the LGM ice-sheet likely led to two significant pulses of magmatic CO2. The first, and most significant of these, is associated with ice-sheet growth and occurs as the magma system recovers from glacial loading. This recovery happens from the base of the melting region upwards, producing a pulse of CO2 rich magma that is predicted to reach the surface around 20 ka after the loading event, close in time to the LGM. The second peak in CO2 output occurs abruptly following deglaciation as a consequence of increased rates of melt generation and transport in the shallow mantle. Although these post-glacial melts are relatively depleted in CO2, the increase in magma flux leads to a short-lived period of elevated CO2 emissions. Our results therefore suggest a negative feedback, whereby ice-sheet growth produces a delayed pulse of magmatic CO2, which, in addition to increased geothermal heat flux, may contribute towards driving deglaciation, which itself then causes further magmatism and CO2 outgassing. This model is consistent with the seismic structure of the asthenosphere below Iceland, and the established compositional and volumetric trends for sub- and post-glacial volcanism in Iceland. These trends show that

Variability of sea salts in ice and firn cores from Fimbul Ice Shelf, Dronning Maud Land, Antarctica

NASA Astrophysics Data System (ADS)

Paulina Vega, Carmen; Isaksson, Elisabeth; Schlosser, Elisabeth; Divine, Dmitry; Martma, Tõnu; Mulvaney, Robert; Eichler, Anja; Schwikowski-Gigar, Margit

2018-05-01

Major ions were analysed in firn and ice cores located at Fimbul Ice Shelf (FIS), Dronning Maud Land - DML, Antarctica. FIS is the largest ice shelf in the Haakon VII Sea, with an extent of approximately 36 500 km2. Three shallow firn cores (about 20 m deep) were retrieved in different ice rises, Kupol Ciolkovskogo (KC), Kupol Moskovskij (KM), and Blåskimen Island (BI), while a 100 m long core (S100) was drilled near the FIS edge. These sites are distributed over the entire FIS area so that they provide a variety of elevation (50-400 m a.s.l.) and distance (3-42 km) to the sea. Sea-salt species (mainly Na+ and Cl-) generally dominate the precipitation chemistry in the study region. We associate a significant sixfold increase in median sea-salt concentrations, observed in the S100 core after the 1950s, to an enhanced exposure of the S100 site to primary sea-salt aerosol due to a shorter distance from the S100 site to the ice front, and to enhanced sea-salt aerosol production from blowing salty snow over sea ice, most likely related to the calving of Trolltunga occurred during the 1960s. This increase in sea-salt concentrations is synchronous with a shift in non-sea-salt sulfate (nssSO42-) toward negative values, suggesting a possible contribution of fractionated aerosol to the sea-salt load in the S100 core most likely originating from salty snow found on sea ice. In contrast, there is no evidence of a significant contribution of fractionated sea salt to the ice-rises sites, where the signal would be most likely masked by the large inputs of biogenic sulfate estimated for these sites. In summary, these results suggest that the S100 core contains a sea-salt record dominated by the proximity of the site to the ocean, and processes of sea ice formation in the neighbouring waters. In contrast, the ice-rises firn cores register a larger-scale signal of atmospheric flow conditions and a less efficient transport of sea-salt aerosols to these sites. These findings are a

The response of Antarctic sea ice algae to changes in pH and CO2.

PubMed

McMinn, Andrew; Müller, Marius N; Martin, Andrew; Ryan, Ken G

2014-01-01

Ocean acidification substantially alters ocean carbon chemistry and hence pH but the effects on sea ice formation and the CO2 concentration in the enclosed brine channels are unknown. Microbial communities inhabiting sea ice ecosystems currently contribute 10-50% of the annual primary production of polar seas, supporting overwintering zooplankton species, especially Antarctic krill, and seeding spring phytoplankton blooms. Ocean acidification is occurring in all surface waters but the strongest effects will be experienced in polar ecosystems with significant effects on all trophic levels. Brine algae collected from McMurdo Sound (Antarctica) sea ice was incubated in situ under various carbonate chemistry conditions. The carbon chemistry was manipulated with acid, bicarbonate and bases to produce a pCO2 and pH range from 238 to 6066 µatm and 7.19 to 8.66, respectively. Elevated pCO2 positively affected the growth rate of the brine algal community, dominated by the unique ice dinoflagellate, Polarella glacialis. Growth rates were significantly reduced when pH dropped below 7.6. However, when the pH was held constant and the pCO2 increased, growth rates of the brine algae increased by more than 20% and showed no decline at pCO2 values more than five times current ambient levels. We suggest that projected increases in seawater pCO2, associated with OA, will not adversely impact brine algal communities.

Ikaite crystal distribution in Arctic winter sea ice and implications for CO2 system dynamics

NASA Astrophysics Data System (ADS)

Rysgaard, S.; Søgaard, D. H.; Cooper, M.; Pućko, M.; Lennert, K.; Papakyriakou, T. N.; Wang, F.; Geilfus, N. X.; Glud, R. N.; Ehn, J.; McGinnnis, D. F.; Attard, K.; Sievers, J.; Deming, J. W.; Barber, D.

2012-12-01

The precipitation of ikaite (CaCO3·6H2O) in polar sea ice is critical to the efficiency of the sea ice-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the ice is poorly known. We report unique observations of ikaite in unmelted ice and vertical profiles of ikaite abundance and concentration in sea ice for the crucial season of winter. Ice was examined from two locations: a 1 m thick land-fast ice site and a 0.3 m thick polynya site, both in the Young Sound area (74° N, 20° W) of NE Greenland. Ikaite crystals, ranging in size from a few µm to 700 µm were observed to concentrate in the interstices between the ice platelets in both granular and columnar sea ice. In vertical sea-ice profiles from both locations, ikaite concentration determined from image analysis, decreased with depth from surfaceice values of 700-900 µmol kg-1 ice (~ 25 × 106 crystals kg-1) to bottom-layer values of 100-200 µmol kg-1 ice (1-7 × 106 kg-1), all of which are much higher (4-10 times) than those reported in the few previous studies. Direct measurements of total alkalinity (TA) in surface layers fell within the same range as ikaite concentration whereas TA concentrations in bottom layers were twice as high. This depth-related discrepancy suggests interior ice processes where ikaite crystals form in surface sea ice layers and partly dissolved in bottom layers. From these findings and model calculations we relate sea ice formation and melt to observed pCO2 conditions in polar surface waters, and hence, the air-sea CO2 flux.

Multisite high resolution measurements of carbon monoxide along Greenland ice cores: evidence for in-situ production and potential for atmospheric reconstruction

NASA Astrophysics Data System (ADS)

Faïn, Xavier; Chappellaz, Jérôme; Rhodes, Rachael; Stowasser, Christopher; Blunier, Thomas; McConnell, Joseph; Brook, Edward; Desbois, Thibault; Romanini, Daniele

2014-05-01

Carbon monoxide (CO) is the principal sink for hydroxyl radicals (OH) in the troposphere. Consequently, changes in atmospheric CO levels can considerably perturb the oxidizing capacity of the atmosphere, affecting mixing ratios of a host of chemical species oxidized by OH, including methane. In addition, CO variations (and changes in its stable isotopic composition) are expected to be good tracers of changes in biomass burning emissions. Investigating past mixing ratios of carbon monoxide is thus a promising approach towards reducing uncertainty related to the past oxidative capacity of the atmosphere and biogeochemical cycling of methane. Recent developments in optical spectrometry (Optical Feedback Cavity Enhanced Absorption Spectrometry, OFCEAS), combined with continuous flow analysis (CFA) systems, allow efficient, precise measurements of CO concentrations in ice cores. Coupling our OFCEAS spectrometer with the CFA melter operated at DRI (Reno, USA) provided the first continuous CO measurements along the NEEM (Greenland) core covering the last 1800 yr at an unprecedented resolution. Although the most recent section of this record (i.e., since 1700 AD) agreed with existing discrete CO measurements from the Eurocore ice core and the deep NEEM firn, it was difficult to interpret in terms of atmospheric CO variation due to high frequency, high amplitudes spikes related to in-situ production (Faïn et al., Climate of the Past Discussion). During a recent 8-week analytical campaign, three different ice archives from Greenland were melted on the DRI CFA and analyzed continuously for CO with the OFCEAS spectrometer: (i) the D4 core (spanning the last 170 yr), (ii) the NEEM core (extending the existing record from 200 AD to 800 BC), and (iii) the Tunu core (spanning the last 1800 yr). Although in-situ production of CO is observed at all sites, these new records reveal different CO patterns and trends. This multisite approach allows us to better characterize the

Landscape Evolution and the Reincarnation of the Residual CO2 Ice Cap of Mars

NASA Astrophysics Data System (ADS)

Byrne, S.; Zuber, M.

2006-12-01

Observations of the southern residual CO2 cap of Mars reveal a wide range of landforms including flat-floored quasi-circular pits with steep walls (dubbed Swiss-cheese features). Interannual comparisons show that these depressions are expanding laterally at rates of ~2m/yr to ~4m/yr, prompting suggestions of climate change. The residual CO2 ice cap is up to 10m thick and underlain by an involatile basement, it also contains layers roughly 2m thick representing different accumulation episodes in the recent past. Changes in the appearance of the residual ice between the Mariner 9 and Viking missions indicate that the top-most layer was deposited in that time-frame, soon after the global dust storm of 1971. The spatial density of the Swiss-cheese features, and the rate at which they expand, mean that it is unlikely that any part of the residual ice cap is older than a few centuries. Given this, we may ask: how can there be a residual cap present today for us to observe? To answer this and other questions we have developed a model to examine the evolution of a CO2 ice landscape. This model reproduces the morphologies and expansion rates seen in the actual residual CO2 ice cap. Our model results indicate that the fate of CO2 ice surfaces is controlled by their surface roughness. Surface roughness always increases with time, which results in an unstable situation. When the surface roughness exceeds a critical point small pits can begin to develop. The walls of these pits rapidly steepen and begin retreating which enlarges and deepens the pit. This situation always occurs even if the surface of the CO2 slab has a high enough albedo to have a net mass gain each year. Once these pits begin expanding they quickly erode the entire ice slab. When the underlying non-CO2 material is exposed, it will not frost over again if Mars were to repeat like clockwork every year. We conclude that interannual climatic variability is actually a requirement for the continued existence of a

Ikaite crystals in melting sea ice - implications for pCO2 and pH levels in Arctic surface waters

NASA Astrophysics Data System (ADS)

Rysgaard, S.; Glud, R. N.; Lennert, K.; Cooper, M.; Halden, N.; Leakey, R. J. G.; Hawthorne, F. C.; Barber, D.

2012-08-01

A major issue of Arctic marine science is to understand whether the Arctic Ocean is, or will be, a source or sink for air-sea CO2 exchange. This has been complicated by the recent discoveries of ikaite (a polymorph of CaCO3·6H2O) in Arctic and Antarctic sea ice, which indicate that multiple chemical transformations occur in sea ice with a possible effect on CO2 and pH conditions in surface waters. Here, we report on biogeochemical conditions, microscopic examinations and x-ray diffraction analysis of single crystals from a melting 1.7 km2 (0.5-1 m thick) drifting ice floe in the Fram Strait during summer. Our findings show that ikaite crystals are present throughout the sea ice but with larger crystals appearing in the upper ice layers. Ikaite crystals placed at elevated temperatures disintegrated into smaller crystallites and dissolved. During our field campaign in late June, melt reduced the ice floe thickness by 0.2 m per week and resulted in an estimated 3.8 ppm decrease of pCO2 in the ocean surface mixed layer. This corresponds to an air-sea CO2 uptake of 10.6 mmol m-2 sea ice d-1 or to 3.3 ton km-2 ice floe week-1. This is markedly higher than the estimated primary production within the ice floe of 0.3-1.3 mmol m-2 sea ice d-1. Finally, the presence of ikaite in sea ice and the dissolution of the mineral during melting of the sea ice and mixing of the melt water into the surface oceanic mixed layer accounted for half of the estimated pCO2 uptake.

UV photoprocessing of CO2 ice: a complete quantification of photochemistry and photon-induced desorption processes

NASA Astrophysics Data System (ADS)

Martín-Doménech, R.; Manzano-Santamaría, J.; Muñoz Caro, G. M.; Cruz-Díaz, G. A.; Chen, Y.-J.; Herrero, V. J.; Tanarro, I.

2015-12-01

Context. Ice mantles that formed on top of dust grains are photoprocessed by the secondary ultraviolet (UV) field in cold and dense molecular clouds. UV photons induce photochemistry and desorption of ice molecules. Experimental simulations dedicated to ice analogs under astrophysically relevant conditions are needed to understand these processes. Aims: We present UV-irradiation experiments of a pure CO2 ice analog. Calibration of the quadrupole mass spectrometer allowed us to quantify the photodesorption of molecules to the gas phase. This information was added to the data provided by the Fourier transform infrared spectrometer on the solid phase to obtain a complete quantitative study of the UV photoprocessing of an ice analog. Methods: Experimental simulations were performed in an ultra-high vacuum chamber. Ice samples were deposited onto an infrared transparent window at 8K and were subsequently irradiated with a microwave-discharged hydrogen flow lamp. After irradiation, ice samples were warmed up until complete sublimation was attained. Results: Photolysis of CO2 molecules initiates a network of photon-induced chemical reactions leading to the formation of CO, CO3, O2, and O3. During irradiation, photon-induced desorption of CO and, to a lesser extent, O2 and CO2 took place through a process called indirect desorption induced by electronic transitions, with maximum photodesorption yields (Ypd) of ~1.2 × 10-2 molecules incident photon-1, ~9.3 × 10-4 molecules incident photon-1, and ~1.1 × 10-4 molecules incident photon-1, respectively. Conclusions: Calibration of mass spectrometers allows a direct quantification of photodesorption yields instead of the indirect values that were obtained from infrared spectra in most previous works. Supplementary information provided by infrared spectroscopy leads to a complete quantification, and therefore a better understanding, of the processes taking place in UV-irradiated ice mantles. Appendix A is available in

High Resolution Continuous Flow Analysis System for Polar Ice Cores

NASA Astrophysics Data System (ADS)

Dallmayr, Remi; Azuma, Kumiko; Yamada, Hironobu; Kjær, Helle Astrid; Vallelonga, Paul; Azuma, Nobuhiko; Takata, Morimasa

2014-05-01

In the last decades, Continuous Flow Analysis (CFA) technology for ice core analyses has been developed to reconstruct the past changes of the climate system 1), 2). Compared with traditional analyses of discrete samples, a CFA system offers much faster and higher depth resolution analyses. It also generates a decontaminated sample stream without time-consuming sample processing procedure by using the inner area of an ice-core sample.. The CFA system that we have been developing is currently able to continuously measure stable water isotopes 3) and electrolytic conductivity, as well as to collect discrete samples for the both inner and outer areas with variable depth resolutions. Chemistry analyses4) and methane-gas analysis 5) are planned to be added using the continuous water stream system 5). In order to optimize the resolution of the current system with minimal sample volumes necessary for different analyses, our CFA system typically melts an ice core at 1.6 cm/min. Instead of using a wire position encoder with typical 1mm positioning resolution 6), we decided to use a high-accuracy CCD Laser displacement sensor (LKG-G505, Keyence). At the 1.6 cm/min melt rate, the positioning resolution was increased to 0.27mm. Also, the mixing volume that occurs in our open split debubbler is regulated using its weight. The overflow pumping rate is smoothly PID controlled to maintain the weight as low as possible, while keeping a safety buffer of water to avoid air bubbles downstream. To evaluate the system's depth-resolution, we will present the preliminary data of electrolytic conductivity obtained by melting 12 bags of the North Greenland Eemian Ice Drilling (NEEM) ice core. The samples correspond to different climate intervals (Greenland Stadial 21, 22, Greenland Stadial 5, Greenland Interstadial 5, Greenland Interstadial 7, Greenland Stadial 8). We will present results for the Greenland Stadial -8, whose depths and ages are between 1723.7 and 1724.8 meters, and 35.520 to

Buried CO2 Ice traces in South Polar Layered Deposits of Mars detected by radar sounder

NASA Astrophysics Data System (ADS)

Castaldo, L.; Mège, D.; Orosei, R.; Séjourné, A.

2014-12-01

SHARAD (SHAllow RADar) is the subsurface sounding radar provided by the Italian Space Agency (ASI) as a facility instrument to NASA's 2005 Mars Reconnaissance Orbiter (MRO). The Reduced Data Record of SHARAD data covering the area of the South Polar Layered Deposits (SPLD), has been used. The elaboration and interpretation of the data, aimed to estimate electromagnetic properties of surface layers, has been performed in terms of permittivity. The theory of electromagnetic scattering from fractal surfaces, and the estimation of geometric parameters from topographic data by Mars Orbiter Laser Altimeter (MOLA) which was one of five instruments on board the Mars Global Surveyor (MGS) spacecraft, has been used. A deep analysis of inversion has been made on all Mars and extended to the South Polar Caps in order to extract the area with a permittivity constant of CO2 ice. Several corrections have been applied to the data, moreover the calibration of the signal requires the determination of a constant that takes into account the power gain due to the radar system and the surface in order to compensate the power losses due to the orbitographic phenomena. The determination of regions with high probability of buried CO2 ice in the first layer of the Martian surface, is obtained extracting the real part of the permittivity constant of the CO2 ice (~2), estimated by other means. The permittivity of CO2ice is extracted from the Global Permittivity Map of Mars using the global standard deviation of itself as following: ɛCO2ice=ɛCO2ice+ Σ (1)where Σ=±std(ɛMapMars)/2Figure 1(a) shows the south polar areas where the values of the permittivity point to the possibility of a CO2 ice layer. Figure 1(b) is the corresponding geologic map. The comparison between the two maps indicates that the area with probable buried CO2 overlaps Hesperian and Amazonian polar units (Hp, Hesperian plains-forming deposits marked by narrow sinuous, anabranching ridges and irregular depressions, and

Devon island ice cap: core stratigraphy and paleoclimate.

PubMed

Koerner, R M

1977-04-01

Valuable paleoclimatic information can be gained by studying the distribution of melt layers in deep ice cores. A profile representing the percentage of ice in melt layers in a core drilled from the Devon Island ice cap plotted against both time and depth shows that the ice cap has experienced a period of very warm summers since 1925, following a period of colder summers between about 1600 and 1925. The earlier period was coldest between 1680 and 1730. There is a high correlation between the melt-layer ice percentage and the mass balance of the ice cap. The relation between them suggests that the ice cap mass balance was zero (accumulation equaled ablation) during the colder period but is negative in the present warmer one. There is no firm evidence of a present cooling trend in the summer conditions on the ice cap. A comparison with the melt-layer ice percentage in cores from the other major Canadian Arctic ice caps shows that the variation of summer conditions found for the Devon Island ice cap is representative for all the large ice caps for about 90 percent of the time. There is also a good correlation between melt-layer percentage and summer sea-ice conditions in the archipelago. This suggests that the search for the northwest passage was influenced by changing climate, with the 19th-century peak of the often tragic exploration coinciding with a period of very cold summers.

H-atom addition and abstraction reactions in mixed CO, H2CO and CH3OH ices - an extended view on complex organic molecule formation

NASA Astrophysics Data System (ADS)

Chuang, K.-J.; Fedoseev, G.; Ioppolo, S.; van Dishoeck, E. F.; Linnartz, H.

2016-01-01

Complex organic molecules (COMs) have been observed not only in the hot cores surrounding low- and high-mass protostars, but also in cold dark clouds. Therefore, it is interesting to understand how such species can be formed without the presence of embedded energy sources. We present new laboratory experiments on the low-temperature solid state formation of three complex molecules - methyl formate (HC(O)OCH3), glycolaldehyde (HC(O)CH2OH) and ethylene glycol (H2C(OH)CH2OH) - through recombination of free radicals formed via H-atom addition and abstraction reactions at different stages in the CO→H2CO→CH3OH hydrogenation network at 15 K. The experiments extend previous CO hydrogenation studies and aim at resembling the physical-chemical conditions typical of the CO freeze-out stage in dark molecular clouds, when H2CO and CH3OH form by recombination of accreting CO molecules and H-atoms on ice grains. We confirm that H2CO, once formed through CO hydrogenation, not only yields CH3OH through ongoing H-atom addition reactions, but is also subject to H-atom-induced abstraction reactions, yielding CO again. In a similar way, H2CO is also formed in abstraction reactions involving CH3OH. The dominant methanol H-atom abstraction product is expected to be CH2OH, while H-atom additions to H2CO should at least partially proceed through CH3O intermediate radicals. The occurrence of H-atom abstraction reactions in ice mantles leads to more reactive intermediates (HCO, CH3O and CH2OH) than previously thought, when assuming sequential H-atom addition reactions only. This enhances the probability to form COMs through radical-radical recombination without the need of UV photolysis or cosmic rays as external triggers.

Ab initio Quantum Chemical Studies of Reactions in Astrophysical Ices. Reactions Involving CH3OH, CO2, CO, HNCO in H2CO/NH3/H2O Ices

NASA Technical Reports Server (NTRS)

Woon, David E.

2006-01-01

While reactions between closed shell molecules generally involve prohibitive barriers in the gas phase, prior experimental and theoretical studies have demonstrated that some of these reactions are significantly enhanced when confined within an icy grain mantle and can occur efficiently at temperatures below 100 K with no additional energy processing. The archetypal case is the reaction of formaldehyde (H2CO) and ammonia (NH3) to yield hydroxymethylamine (NH2CH2OH). In the present work we have characterized reactions involving methanol (CH3OH), carbon dioxide (CO2), carbon monoxide (CO), and isocyanic acid (HNCO) in search of other favorable cases. Most of the emphasis is on CH3OH, which was investigated in the two-body reaction with one H2CO and the three-body reaction with two H2CO molecules. The addition of a second H2CO to the product of the reaction between CH3OH and H2CO was also considered as an alternative route to longer polyoxymethylene polymers of the -CH2O- form. The reaction between HNCO and NH3 was studied to determine if it can compete against the barrierless charge transfer process that yields OCN(-) and NH4(+). Finally, the H2CO + NH3 reaction was revisited with additional benchmark calculations that confirm that little or no barrier is present when it occurs in ice.

POLLiCE (POLLen in the iCE): climate history from Adamello ice cores

NASA Astrophysics Data System (ADS)

Cristofori, Antonella; Festi, Daniela; Maggi, Valter; Casarotto, Christian; Bertoni, Elena; Vernesi, Cristiano

2017-04-01

Glaciers can be viewed as the most complete and effective past climate and environment archives severely threatened by climate change. These threats are particularly dramatic across European Alps. The Adamello glacier is the largest, 16.4 km2, and deepest, 270 m, Italian glacier. We aim at estimating biodiversity changes over the last centuries in relation to climate and human activities in the Adamello catchment area. We, therefore, recently launched the POLLiCE project (pollice.fmach.it) for specifically targeting the biological component (e.g. pollen, leaves, plant remains) trapped in ice cores. Classical morphological pollen analysis will be accompanied by DNA metabarcoding. This approach has the potential to provide a detailed taxonomical identification - at least genus level- thus circumventing the limitations of microscopic analysis such as time-consuming procedures and shared features of pollen grains among different taxa. Moreover, ice cores are subjected to chemical and physical analyses - stable isotopes, ions, hyperspectral imaging, etc.- for stratigraphic and climatic determination of seasonality. A pilot drilling was conducted on March 2015 and the resulting 5 m core has been analysed in terms of pollen spectrum, stable isotopes and ions in order to demonstrate the feasibility of the study. The first encouraging results showed that even in this superficial core a stratigraphy is evident with indication of seasonality as highlighted by both by pollen taxa and stable isotopes. Finally, DNA has been successfully extracted and amplified with specific DNA barcodes. A medium drilling was performed on April 2016 with the extraction of a 45 m ice core. The analysis of this core constitutes the subject of a specific research project, CALICE*, just funded by Euregio Science Fund (IPN57). The entire depth, 270 m, of the Adamello glacier is scheduled to be drilled in 2018 winter to secure the unique memory archived by the ice. * See EGU2017 poster by Festi et al

Dust Records in Ice Cores from the Tibetan Plateau

NASA Astrophysics Data System (ADS)

Wang, N.; Yao, T.; Thompson, L. G.

2014-12-01

Dust plays an important role in the Earth system, and it usually displays largely spatial and temporal variations. It is necessary for us to reconstruct the past variations of dust in different regions to better understand the interactions between dust and environments. Ice core records can reveal the history of dust variations. In this paper, we used the Guliya, Dunde, Malan and Dasuopu ice cores from the Tibetan Plateau to study the spatial distribution, the seasonal variations and the secular trends of dust. It was found that the mean dust concentration was higher by one or two order of magnitudes in the Guliya and Dunde ice cores from the northern Tibetan Plateau than in the Dasuopu ice core from the southern Tibetan Plateau. During the year, the highest dust concentration occurs in the springtime in the northern Tibetan Plateau while in the non-monsoon season in the southern Tibetan Plateau. Over the last millennium, the Dasuopu ice core record shows that the 1270s~1380s and 1870s~1990s were the two epochs with high dust concentration. However, the Malan ice core from the northern Tibetan Plateau indicates that high dust concentration occurred in the 1130s~1550s and 1770s~1940s. Interestingly, climatic and environmental records of the ice cores from the Tibetan Plateau reflected that the correlation between dust concentration and air temperature was strongly positive in the southern Plateau while negative in the northern Plateau over the last millennium. This implies that climatic and environmental changes existed considerable differences in the different parts of the Plateau. Moreover, four Asian megadroughts occurred in 1638~1641, 1756~1758, 1790~1796 and 1876~1878, which caused more than tens millions people died, were revealed clearly by dust record in the Dasuopu ice core.

How Will Sea Ice Loss Affect the Greenland Ice Sheet? On the Puzzling Features of Greenland Ice-Core Isotopic Composition

NASA Technical Reports Server (NTRS)

Pausata, Francesco S. R.; Legrande, Allegra N.; Roberts, William H. G.

2016-01-01

The modern cryosphere, Earth's frozen water regime, is in fast transition. Greenland ice cores show how fast theses changes can be, presenting evidence of up to 15 C warming events over timescales of less than a decade. These events, called Dansgaard/Oeschger (D/O) events, are believed to be associated with rapid changes in Arctic sea ice, although the underlying mechanisms are still unclear. The modern demise of Arctic sea ice may, in turn, instigate abrupt changes on the Greenland Ice Sheet. The Arctic Sea Ice and Greenland Ice Sheet Sensitivity (Ice2Ice Chttps://ice2ice.b.uib.noD) initiative, sponsored by the European Research Council, seeks to quantify these past rapid changes to improve our understanding of what the future may hold for the Arctic. Twenty scientists gathered in Copenhagen as part of this initiative to discuss the most recent observational, technological, and model developments toward quantifying the mechanisms behind past climate changes in Greenland. Much of the discussion focused on the causes behind the changes in stable water isotopes recorded in ice cores. The participants discussed sources of variability for stable water isotopes and framed ways that new studies could improve understanding of modern climate. The participants also discussed how climate models could provide insights into the relative roles of local and nonlocal processes in affecting stable water isotopes within the Greenland Ice Sheet. Presentations of modeling results showed how a change in the source or seasonality of precipitation could occur not only between glacial and modern climates but also between abrupt events. Recent fieldwork campaigns illustrate an important role of stable isotopes in atmospheric vapor and diffusion in the final stable isotope signal in ice. Further, indications from recent fieldwork campaigns illustrate an important role of stable isotopes in atmospheric vapor and diffusion in the final stable isotope signal in ice. This feature complicates

IceChrono1: a probabilistic model to compute a common and optimal chronology for several ice cores

NASA Astrophysics Data System (ADS)

Parrenin, F.; Bazin, L.; Capron, E.; Landais, A.; Lemieux-Dudon, B.; Masson-Delmotte, V.

2015-05-01

Polar ice cores provide exceptional archives of past environmental conditions. The dating of ice cores and the estimation of the age-scale uncertainty are essential to interpret the climate and environmental records that they contain. It is, however, a complex problem which involves different methods. Here, we present IceChrono1, a new probabilistic model integrating various sources of chronological information to produce a common and optimized chronology for several ice cores, as well as its uncertainty. IceChrono1 is based on the inversion of three quantities: the surface accumulation rate, the lock-in depth (LID) of air bubbles and the thinning function. The chronological information integrated into the model are models of the sedimentation process (accumulation of snow, densification of snow into ice and air trapping, ice flow), ice- and air-dated horizons, ice and air depth intervals with known durations, depth observations (depth shift between synchronous events recorded in the ice and in the air) and finally air and ice stratigraphic links in between ice cores. The optimization is formulated as a least squares problem, implying that all densities of probabilities are assumed to be Gaussian. It is numerically solved using the Levenberg-Marquardt algorithm and a numerical evaluation of the model's Jacobian. IceChrono follows an approach similar to that of the Datice model which was recently used to produce the AICC2012 (Antarctic ice core chronology) for four Antarctic ice cores and one Greenland ice core. IceChrono1 provides improvements and simplifications with respect to Datice from the mathematical, numerical and programming point of views. The capabilities of IceChrono1 are demonstrated on a case study similar to the AICC2012 dating experiment. We find results similar to those of Datice, within a few centuries, which is a confirmation of both IceChrono1 and Datice codes. We also test new functionalities with respect to the original version of Datice

Air content and O2/N2 tuned chronologies on local insolation signatures in the Vostok ice core are similar

NASA Astrophysics Data System (ADS)

Lipenkov, V.; Raynaud, D.; Loutre, M.-F.; Duval, P.; Lemieux-Dudon, B.

2009-04-01

An accurate chronology of ice cores is needed for interpreting the paleoclimatic record and understanding the relation between insolation and climate. A new domain of research in this area has been initially stimulated by the work of M. Bender (2002) linking the record of O2/N2 ratio in the air trapped in the Vostok ice with the local insolation. More recently, it has been proposed that the long-term changes in air content, V, recorded in ice from the high Antarctic plateau is also dominantly imprinted by the local summer insolation (Raynaud et al., 2007). The present paper presents a new V record from Vostok, which is compared with the published Vostok O2/N2 record for the same period of time (150-400 ka BP) by using the same spectral analysis methods. The spectral differences between the two properties and the possible mechanisms linking them with insolation through the surface snow structure and the close-off processes are discussed. The main result of our study is that the two experimentally independent local insolation proxies lead to absolute (orbital) time scales, which agree together within a standard deviation of 0.6 ka. This result strongly adds credibility to the air content of ice and the O2 to N2 ratio of the air trapped in ice as equally reliable and complementary tools for accurate dating of existing and future deep ice cores. References: M. Bender, Orbital tuning chronology for the Vostok climate record supported by trapped gas composition, Earth and Planetary Science Letters 204(2002) 275-289. D. Raynaud, V. Lipenkov, B. Lemieux-Dudon, P. Duval, M.F. Loutre, N. Lhomme, The local insolation signature of air content in Antarctic ice: a new step toward an absolute dating of ice records, Earth and Planetary Science Letters 261(2007) 337-349.

Pre-cometary ice composition from hot core chemistry.

PubMed

Tornow, Carmen; Kührt, Ekkehard; Motschmann, Uwe

2005-10-01

Pre-cometary ice located around star-forming regions contains molecules that are pre-biotic compounds or pre-biotic precursors. Molecular line surveys of hot cores provide information on the composition of the ice since it sublimates near these sites. We have combined a hydrostatic hot core model with a complex network of chemical reactions to calculate the time-dependent abundances of molecules, ions, and radicals. The model considers the interaction between the ice and gas phase. It is applied to the Orion hot core where high-mass star formation occurs, and to the solar-mass binary protostar system IRAS 16293-2422. Our calculations show that at the end of the hot core phase both star-forming sites produce the same prebiotic CN-bearing molecules. However, in the Orion hot core these molecules are formed in larger abundances. A comparison of the calculated values with the abundances derived from the observed line data requires a chemically unprocessed molecular cloud as the initial state of hot core evolution. Thus, it appears that these objects are formed at a much younger cloud stage than previously thought. This implies that the ice phase of the young clouds does not contain CN-bearing molecules in large abundances before the hot core has been formed. The pre-biotic molecules synthesized in hot cores cause a chemical enrichment in the gas phase and in the pre-cometary ice. This enrichment is thought to be an important extraterrestrial aspect of the formation of life on Earth and elsewhere.

Towards multi-decadal to multi-millennial ice core records from coastal west Greenland ice caps

NASA Astrophysics Data System (ADS)

Das, Sarah B.; Osman, Matthew B.; Trusel, Luke D.; McConnell, Joseph R.; Smith, Ben E.; Evans, Matthew J.; Frey, Karen E.; Arienzo, Monica; Chellman, Nathan

2017-04-01

The Arctic region, and Greenland in particular, is undergoing dramatic change as characterized by atmospheric warming, decreasing sea ice, shifting ocean circulation patterns, and rapid ice sheet mass loss, but longer records are needed to put these changes into context. Ice core records from the Greenland ice sheet have yielded invaluable insight into past climate change both regionally and globally, and provided important constraints on past surface mass balance more directly, but these ice cores are most often from the interior ice sheet accumulation zone, at high altitude and hundreds of kilometers from the coast. Coastal ice caps, situated around the margins of Greenland, have the potential to provide novel high-resolution records of local and regional maritime climate and sea surface conditions, as well as contemporaneous glaciological changes (such as accumulation and surface melt history). But obtaining these records is extremely challenging. Most of these ice caps are unexplored, and thus their thickness, age, stratigraphy, and utility as sites of new and unique paleoclimate records is largely unknown. Access is severely limited due to their high altitude, steep relief, small surface area, and inclement weather. Furthermore, their relatively low elevation and marine moderated climate can contribute to significant surface melting and degradation of the ice stratigraphy. We recently targeted areas near the Disko Bay region of central west Greenland where maritime ice caps are prevalent but unsampled, as potential sites for new multi-decadal to multi-millennial ice core records. In 2014 & 2015 we identified two promising ice caps, one on Disko Island (1250 m. asl) and one on Nuussuaq Peninsula (1980 m. asl) based on airborne and ground-based geophysical observations and physical and glaciochemical stratigraphy from shallow firn cores. In spring 2015 we collected ice cores at both sites using the Badger-Eclipse electromechanical drill, transported by a medley

The alkenone method for pCO2 reconstructions: challenges and strategies

NASA Astrophysics Data System (ADS)

Zhang, Y.; Pearson, A.; Benthien, A.; Dong, L.; Henderiks, J.; Huybers, P. J.

2016-12-01

The alkenone-pCO2 method is one of the most widely used approaches to reconstruct atmospheric CO2 in the Cenozoic. The method depends upon fractionation of stable carbon isotopes, expressed as ɛp37:2, and a physiological scaling parameter, b, that accounts for algal growth rate and cell size. Alkenone-derived CO2 records for the late Pleistocene, however, often are poorly correlated with ice core CO2 records. We show that poor correlation largely results from (1) systematic overestimation of b and (2) low sensitivity of ɛp37:2 to atmospheric CO2 variations at low-productivity sites [1]. Records are presented from two sites with high ɛp37:2 sensitivity: the South China Sea (SCS) and the tropical Altantic Ocean. Values of b are back calculated to determine their full range over glacial-interglacial cycles using ɛp37:2, ice core pCO2 records, and ocean temperature reconstructions. Air-sea equilibrium of CO2 is assumed at both sites, and the high-resolution temperature record from the SCS site is tuned to ice core pCO2 to eliminate age model discrepancies. The mean value of b is applied to obtain pCO2 estimates. By definition, this approach must yield the correct mean value for pCO2, but observed amplitudes are also reproduced. We further explore the relationship between coccolithophore cell size and growth rate using coccolith size measurements and back-calculated values of b, which suggests a potential proxy to constrain the history of phytoplankton growth rate and b. [1] Zhang, Y.G., Pearson, A., Huybers, P. and Pagani, M, 2016, Refining the alkenone-pCO2 method: The role of algal growth conditions, Paleoceanography, in review

On the size dependence of the scattering greenhouse effect of CO2 ice particles

NASA Astrophysics Data System (ADS)

Kitzmann, D.; Patzer, A. B. C.; Rauer, H.

2011-10-01

In this contribution we study the potential greenhouse effect due to scattering of CO2 ice clouds for atmospheric conditions of terrestrial extrasolar planets. Therefore, we calculate the scattering and absorption properties of CO2 ice particles using Mie theory for assumed particle size distributions with different effective radii and particle densities to determine the scattering and absorption characteristics of such clouds. Implications especially in view of a potential greenhouse warming of the planetary surface are discussed.

Synchronous change of atmospheric CO2 and Antarctic temperature during the last deglacial warming.

PubMed

Parrenin, F; Masson-Delmotte, V; Köhler, P; Raynaud, D; Paillard, D; Schwander, J; Barbante, C; Landais, A; Wegner, A; Jouzel, J

2013-03-01

Understanding the role of atmospheric CO2 during past climate changes requires clear knowledge of how it varies in time relative to temperature. Antarctic ice cores preserve highly resolved records of atmospheric CO2 and Antarctic temperature for the past 800,000 years. Here we propose a revised relative age scale for the concentration of atmospheric CO2 and Antarctic temperature for the last deglacial warming, using data from five Antarctic ice cores. We infer the phasing between CO2 concentration and Antarctic temperature at four times when their trends change abruptly. We find no significant asynchrony between them, indicating that Antarctic temperature did not begin to rise hundreds of years before the concentration of atmospheric CO2, as has been suggested by earlier studies.

Ikaite crystals in melting sea ice - implications for pCO2 and pH levels in Arctic surface waters

NASA Astrophysics Data System (ADS)

Rysgaard, S.; Glud, R. N.; Lennert, K.; Cooper, M.; Halden, N.; Leakey, R. J. G.; Hawthorne, F. C.; Barber, D.

2012-03-01

A major issue of Arctic marine science is to understand whether the Arctic Ocean is, or will be, a source or sink for air-sea CO2 exchange. This has been complicated by the recent discoveries of ikaite (CaCO3·6H2O) in Arctic and Antarctic sea ice, which indicate that multiple chemical transformations occur in sea ice with a possible effect on CO2 and pH conditions in surface waters. Here we report on biogeochemical conditions, microscopic examinations and x-ray diffraction analysis of single crystals from an actively melting 1.7 km2 (0.5-1 m thick) drifting ice floe in the Fram Strait during summer. Our findings show that ikaite crystals are present throughout the sea ice but with larger crystals appearing in the upper ice layers. Ikaite crystals placed at elevated temperatures gradually disintegrated into smaller crystallites and dissolved. During our field campaign in late June, melt reduced the ice flow thickness by ca. 0.2 m per week and resulted in an estimated 1.6 ppm decrease of pCO2 in the ocean surface mixed layer. This corresponds to an air-sea CO2 uptake of 11 mmol m-2 sea ice d-1 or to 3.5 ton km-2 ice floe week-1.

Methane and nitrous oxide in the ice core record.

PubMed

Wolff, Eric; Spahni, Renato

2007-07-15

Polar ice cores contain, in trapped air bubbles, an archive of the concentrations of stable atmospheric gases. Of the major non-CO2 greenhouse gases, methane is measured quite routinely, while nitrous oxide is more challenging, with some artefacts occurring in the ice and so far limited interpretation. In the recent past, the ice cores provide the only direct measure of the changes that have occurred during the industrial period; they show that the current concentration of methane in the atmosphere is far outside the range experienced in the last 650,000 years; nitrous oxide is also elevated above its natural levels. There is controversy about whether changes in the pre-industrial Holocene are natural or anthropogenic in origin. Changes in wetland emissions are generally cited as the main cause of the large glacial-interglacial change in methane. However, changing sinks must also be considered, and the impact of possible newly described sources evaluated. Recent isotopic data appear to finally rule out any major impact of clathrate releases on methane at these time-scales. Any explanation must take into account that, at the rapid Dansgaard-Oeschger warmings of the last glacial period, methane rose by around half its glacial-interglacial range in only a few decades. The recent EPICA Dome C (Antarctica) record shows that methane tracked climate over the last 650,000 years, with lower methane concentrations in glacials than interglacials, and lower concentrations in cooler interglacials than in warmer ones. Nitrous oxide also shows Dansgaard-Oeschger and glacial-interglacial periodicity, but the pattern is less clear.

TRACEing Last Glacial Period (25-80 ka b2k) tephra horizons within North Atlantic marine cores and exploring links to the Greenland ice-cores

NASA Astrophysics Data System (ADS)

Abbott, P. M.; Davies, S. M.; Griggs, A. J.; Bourne, A. J.; Cook, E.; Pearce, N. J. G.; Austin, W. E. N.; Chapman, M.; Hall, I. R.; Purcell, C. S.; Scourse, J. D.; Rasmussen, T. L.

2015-12-01

Tephrochronology is a powerful technique for the correlation and synchronisation of disparate palaeoclimatic records from different depositional environments and has considerable potential for testing climatic phasing. For example, the relative timing of atmospheric and marine changes caused by the abrupt climatic events that punctuated the last glacial period within the North Atlantic region. Here we report on efforts to establish a framework of tephra horizons within North Atlantic marine sequences that can correlate these records and if traced in the Greenland ice-cores can act as isochronous tie-lines. Investigations have been conducted on a network of marine cores from a number of sites across the North Atlantic. Tephra horizons have been identified using cryptotephra extraction techniques more commonly applied to the study of terrestrial sequences. There are two main challenges with assessing cryptotephras in the glacial North Atlantic; i) determining the transportation processes and ii) assessing the influence of secondary reworking processes and the stratigraphic integrity of the isochrons. These processes and their influence are investigated for each cryptotephra using shard size variations, major element heterogeneity and co-variance of IRD input for some cores. Numerous Icelandic cryptophras have been successfully identified in the marine records and we will discuss the integration of a number of these with an isochronous nature into a marine tephra framework and how potential correlations to the Greenland ice-core tephra framework are determined. Spatial patterns in the nature of tephra records that are emerging from the core network will be highlighted to outline some of the key areas that could be explored in the future. In addition, the synchronisation of multiple North Atlantic records to the Greenland ice-cores using the North Atlantic Ash Zone II to test the synchroneity of an abrupt cooling in the North Atlantic will be discussed.

Interannual observations and quantification of summertime H2O ice deposition on the Martian CO2 ice south polar cap

USGS Publications Warehouse

Brown, Adrian J.; Piqueux, Sylvain; Titus, Timothy N.

2014-01-01

The spectral signature of water ice was observed on Martian south polar cap in 2004 by the Observatoire pour l'Mineralogie, l'Eau les Glaces et l'Activite (OMEGA) ( Bibring et al., 2004). Three years later, the OMEGA instrument was used to discover water ice deposited during southern summer on the polar cap ( Langevin et al., 2007). However, temporal and spatial variations of these water ice signatures have remained unexplored, and the origins of these water deposits remains an important scientific question. To investigate this question, we have used observations from the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) instrument on the Mars Reconnaissance Orbiter (MRO) spacecraft of the southern cap during austral summer over four Martian years to search for variations in the amount of water ice. We report below that for each year we have observed the cap, the magnitude of the H2O ice signature on the southern cap has risen steadily throughout summer, particularly on the west end of the cap. The spatial extent of deposition is in disagreement with the current best simulations of deposition of water ice on the south polar cap (Montmessin et al., 2007). This increase in water ice signatures is most likely caused by deposition of atmospheric H2O ice and a set of unusual conditions makes the quantification of this transport flux using CRISM close to ideal. We calculate a ‘minimum apparent‘ amount of deposition corresponding to a thin H2O ice layer of 0.2 mm (with 70% porosity). This amount of H2O ice deposition is 0.6–6% of the total Martian atmospheric water budget. We compare our ‘minimum apparent’ quantification with previous estimates. This deposition process may also have implications for the formation and stability of the southern CO2 ice cap, and therefore play a significant role in the climate budget of modern day Mars.

Detection of Organic Matter in Greenland Ice Cores by Deep-UV Fluorescence

NASA Astrophysics Data System (ADS)

Willis, M.; Malaska, M.; Wanger, G.; Bhartia, R.; Eshelman, E.; Abbey, W.; Priscu, J. C.

2017-12-01

The Greenland Ice Sheet is an Earthly analog for icy ocean worlds in the outer Solar System. Future missions to such worlds including Europa, Enceladus, and Titan may potentially include spectroscopic instrumentation to examine the surface/subsurface. The primary goal of our research is to test deep UV/Raman systems for in the situ detection and localization of organics in ice. As part of this effort we used a deep-UV fluorescence instrument able to detect naturally fluorescent biological materials such as aromatic molecules found in proteins and whole cells. We correlated these data with more traditional downstream analyses of organic material in natural ices. Supraglacial ice cores (2-4 m) were collected from several sites on the southwest outlet of the Greenland Ice Sheet using a 14-cm fluid-free mechanical coring system. Repeat spectral mapping data were initially collected longitudinally on uncut core sections. Cores were then cut into 2 cm thick sections along the longitudinal axis, slowly melted and analyzed for total organic carbon (TOC), total dissolved nitrogen (TDN), and bacterial density. These data reveal a spatial correlation between organic matter concentration, cell density, and the deep UV fluorescence maps. Our results provide a profile of the organics embedded within the ice from the top surface into the glacial subsurface, and the TOC:TDN data from the clean interior of the cores are indicative of a biological origin. This work provides a background dataset for future work to characterize organic carbon in the Greenland Ice Sheet and validation of novel instrumentation for in situ data collection on icy bodies.

Low-latitude ice cores and freshwater availability

NASA Astrophysics Data System (ADS)

Kehrwald, Natalie Marie

2009-12-01

Recent retreat of Tibetan Plateau glaciers affects at least half a billion people. Himalayan glaciers seasonally release meltwater into tributaries of the Indus, Ganges, and Brahmaputra Rivers and supply freshwater necessary to support agricultural and economic practices. Tibetan Plateau glaciers are retreating more rapidly than mountain glaciers elsewhere in the world, and this retreat is accelerating. The Naimona'nyi (30°27'N; 81°91'E, 6050 m a.s.l), Guliya (35°17'N; 81°29'E, 6710 m a.s.l.) and Dasuopu (28°23'N; 85°43'E, 7200 m a.s.l.) ice cores place this recent retreat into a longer time perspective through quantifying climate parameters such as past temperature, aridity, and atmospheric chemistry. Naimona'nyi has not accumulated mass since at least 1950, as evidenced by the virtual lack of radiogenic isotopes (36Cl, 3 H, and beta radioactivity) present in the ice core. These isotopes were produced by U.S. and Soviet atmospheric thermonuclear bomb tests conducted in the 1950s and 1960s and provide independent dating horizons for the ice cores. Lead-210 dates imply that the uppermost preserved glacial ice on Naimona'nyi formed during the 1940s. While this is the highest documented glacial thinning in the world other glaciers at elevations similar to that of Naimona'nyi, such as Kilimanjaro (3°4'S; 37°21'E, 5893 m a.s.l.), are also losing mass at their summits. The global scope of high-elevation glacial thinning suggests that ablation on the Earth's highest ice fields may be more prevalent as global mean temperatures continue to increase. Glacial thinning has not been taken into account in future projections of regional freshwater availability, and the net mass loss indicates that Himalayan glaciers currently store less freshwater than assumed in models. The acceleration of Tibetan Plateau glacial retreat has been hypothesized to be due in part to deposition of black carbon (BC) from biomass burning on to ice fields, thereby lowering the reflectivity of

IceChrono1: a probabilistic model to compute a common and optimal chronology for several ice cores

NASA Astrophysics Data System (ADS)

Parrenin, Frédéric; Bazin, Lucie; Capron, Emilie; Landais, Amaëlle; Lemieux-Dudon, Bénédicte; Masson-Delmotte, Valérie

2016-04-01

Polar ice cores provide exceptional archives of past environmental conditions. The dating of ice cores and the estimation of the age scale uncertainty are essential to interpret the climate and environmental records that they contain. It is however a complex problem which involves different methods. Here, we present IceChrono1, a new probabilistic model integrating various sources of chronological information to produce a common and optimized chronology for several ice cores, as well as its uncertainty. IceChrono1 is based on the inversion of three quantities: the surface accumulation rate, the Lock-In Depth (LID) of air bubbles and the thinning function. The chronological information integrated into the model are: models of the sedimentation process (accumulation of snow, densification of snow into ice and air trapping, ice flow), ice and air dated horizons, ice and air depth intervals with known durations, Δdepth observations (depth shift between synchronous events recorded in the ice and in the air) and finally air and ice stratigraphic links in between ice cores. The optimization is formulated as a least squares problem, implying that all densities of probabilities are assumed to be Gaussian. It is numerically solved using the Levenberg-Marquardt algorithm and a numerical evaluation of the model's Jacobian. IceChrono follows an approach similar to that of the Datice model which was recently used to produce the AICC2012 chronology for 4 Antarctic ice cores and 1 Greenland ice core. IceChrono1 provides improvements and simplifications with respect to Datice from the mathematical, numerical and programming point of views. The capabilities of IceChrono is demonstrated on a case study similar to the AICC2012 dating experiment. We find results similar to those of Datice, within a few centuries, which is a confirmation of both IceChrono and Datice codes. We also test new functionalities with respect to the original version of Datice: observations as ice intervals

Canadian Arctic sea ice reconstructed from bromine in the Greenland NEEM ice core.

PubMed

Spolaor, Andrea; Vallelonga, Paul; Turetta, Clara; Maffezzoli, Niccolò; Cozzi, Giulio; Gabrieli, Jacopo; Barbante, Carlo; Goto-Azuma, Kumiko; Saiz-Lopez, Alfonso; Cuevas, Carlos A; Dahl-Jensen, Dorthe

2016-09-21

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 amplification drives Arctic temperatures beyond the 2 °C global average warming target of the recent COP21 Paris climate agreement.

Reassessment of the Upper Fremont Glacier Ice-Core Chronologies by Synchronizing of Ice-Core-Water Isotopes to a Nearby Tree-Ring Chronology.

PubMed

Chellman, Nathan; McConnell, Joseph R; Arienzo, Monica; Pederson, Gregory T; Aarons, Sarah M; Csank, Adam

2017-04-18

The Upper Fremont Glacier (UFG), Wyoming, is one of the few continental glaciers in the contiguous United States known to preserve environmental and climate records spanning recent centuries. A pair of ice cores taken from UFG have been studied extensively to document changes in climate and industrial pollution (most notably, mid-19th century increases in mercury pollution). Fundamental to these studies is the chronology used to map ice-core depth to age. Here, we present a revised chronology for the UFG ice cores based on new measurements and using a novel dating approach of synchronizing continuous water isotope measurements to a nearby tree-ring chronology. While consistent with the few unambiguous age controls underpinning the previous UFG chronologies, the new interpretation suggests a very different time scale for the UFG cores with changes of up to 80 years. Mercury increases previously associated with the mid-19th century Gold Rush now coincide with early-20th century industrial emissions, aligning the UFG record with other North American mercury records from ice and lake sediment cores. Additionally, new UFG records of industrial pollutants parallel changes documented in ice cores from southern Greenland, further validating the new UFG chronologies while documenting the extent of late 19th and early 20th century pollution in remote North America.

Reassessment of the Upper Fremont Glacier ice-core chronologies by synchronizing of ice-core-water isotopes to a nearby tree-ring chronology

USGS Publications Warehouse

Chellman, Nathan J.; McConnell, Joseph R.; Arienzo, Monica; Pederson, Gregory T.; Aarons, Sarah; Csank, Adam

2017-01-01

The Upper Fremont Glacier (UFG), Wyoming, is one of the few continental glaciers in the contiguous United States known to preserve environmental and climate records spanning recent centuries. A pair of ice cores taken from UFG have been studied extensively to document changes in climate and industrial pollution (most notably, mid-19th century increases in mercury pollution). Fundamental to these studies is the chronology used to map ice-core depth to age. Here, we present a revised chronology for the UFG ice cores based on new measurements and using a novel dating approach of synchronizing continuous water isotope measurements to a nearby tree-ring chronology. While consistent with the few unambiguous age controls underpinning the previous UFG chronologies, the new interpretation suggests a very different time scale for the UFG cores with changes of up to 80 years. Mercury increases previously associated with the mid-19th century Gold Rush now coincide with early-20th century industrial emissions, aligning the UFG record with other North American mercury records from ice and lake sediment cores. Additionally, new UFG records of industrial pollutants parallel changes documented in ice cores from southern Greenland, further validating the new UFG chronologies while documenting the extent of late 19th and early 20th century pollution in remote North America.

Physical analysis of an Antarctic ice core-towards an integration of micro- and macrodynamics of polar ice*

NASA Astrophysics Data System (ADS)

Weikusat, Ilka; Jansen, Daniela; Binder, Tobias; Eichler, Jan; Faria, Sérgio H.; Wilhelms, Frank; Kipfstuhl, Sepp; Sheldon, Simon; Miller, Heinrich; Dahl-Jensen, Dorthe; Kleiner, Thomas

2017-02-01

Microstructures from deep ice cores reflect the dynamic conditions of the drill location as well as the thermodynamic history of the drill site and catchment area in great detail. Ice core parameters (crystal lattice-preferred orientation (LPO), grain size, grain shape), mesostructures (visual stratigraphy) as well as borehole deformation were measured in a deep ice core drilled at Kohnen Station, Dronning Maud Land (DML), Antarctica. These observations are used to characterize the local dynamic setting and its rheological as well as microstructural effects at the EDML ice core drilling site (European Project for Ice Coring in Antarctica in DML). The results suggest a division of the core into five distinct sections, interpreted as the effects of changing deformation boundary conditions from triaxial deformation with horizontal extension to bedrock-parallel shear. Region 1 (uppermost approx. 450 m depth) with still small macroscopic strain is dominated by compression of bubbles and strong strain and recrystallization localization. Region 2 (approx. 450-1700 m depth) shows a girdle-type LPO with the girdle plane being perpendicular to grain elongations, which indicates triaxial deformation with dominating horizontal extension. In this region (approx. 1000 m depth), the first subtle traces of shear deformation are observed in the shape-preferred orientation (SPO) by inclination of the grain elongation. Region 3 (approx. 1700-2030 m depth) represents a transitional regime between triaxial deformation and dominance of shear, which becomes apparent in the progression of the girdle to a single maximum LPO and increasing obliqueness of grain elongations. The fully developed single maximum LPO in region 4 (approx. 2030-2385 m depth) is an indicator of shear dominance. Region 5 (below approx. 2385 m depth) is marked by signs of strong shear, such as strong SPO values of grain elongation and strong kink folding of visual layers. The details of structural observations are

Trapping of CH4, CO, and CO2 in Amorphous Water Ice

NASA Astrophysics Data System (ADS)

Mastrapa, R. M. E.; Brown, R. H.; Anicich, V. G.; Cohen, B. A.; Dai, W.; Lunine, J. I.

1999-09-01

In this study, CO, CH4, and CO2 were trapped in H2O at temperatures as low as 20 K and pressures between 10-5 and 10-8 Torr. IR spectra were taken of each sample before sublimation to confirm the presence of volatiles. The samples were then heated at rates from 0.25 K/min to 1 K/min and the escape ranges were measured with a mass spectrometer. The volatiles escaped from the ice mixtures in temperature ranges similar to those found in previous work (1, 2, 3), namely 48-52 K, 145-160 K, 170-185 K. H2O is released from 150 K to 185 K. However, the temperature range of escape is strongly dependent on deposition temperature and heating rate. If the deposition temperature is below the point where the solid volatile rapidly sublimates in the ambient environment of our experiment, then the first range of volatile escape is centered around it's sublimation point, and there is little of the volatile remaining from 170-185 K. The location of the third escape range shifts to lower temperatures with slower sublimation rate. It was determined that 0.5 K/min is the ideal sample heating rate to determine these escape ranges. In our data, the infrared spectrum of CO trapped in water ice shows a splitting of the 2145 cm-1 solid CO line into two bands at 2343 cm-1 and 2135 cm-1. These shifts are similar to those seen by Sandford, et al. (4). (1) Bar-Nun, A., G. Herman, D. Laufer, and M. L. Rappaport, (1985), Icarus, 63, 317-332. (2) Bar-Nun, A., J. Dror, E. Kochavi, and D. Laufer, (1987), Physical Review B, 35, no. 5, 2427-2435. (3) Hudson, R. L., and B. Donn, (1991), Icarus, 94, 326-332. (4) Sandford, S. A., L. J. Allamandola, A. G. G. M. Tielens, and G. J. Valero, (1988), Astrophysical Journal, 329, 498-510.

Neutrino oscillation studies with IceCube-DeepCore

DOE Office of Scientific and Technical Information (OSTI.GOV)

Aartsen, M. G.; Abraham, K.; Ackermann, M.

IceCube, a gigaton-scale neutrino detector located at the South Pole, was primarily designed to search for astrophysical neutrinos with energies of PeV and higher. This goal has been achieved with the detection of the highest energy neutrinos to date. At the other end of the energy spectrum, the DeepCore extension lowers the energy threshold of the detector to approximately 10 GeV and opens the door for oscillation studies using atmospheric neutrinos. An analysis of the disappearance of these neutrinos has been completed, with the results produced being complementary with dedicated oscillation experiments. Following a review of the detector principle andmore » performance, the method used to make these calculations, as well as the results, is detailed. Finally, the future prospects of IceCube-DeepCore and the next generation of neutrino experiments at the South Pole (IceCube-Gen2, specifically the PINGU sub-detector) are briefly discussed.« less

Neutrino oscillation studies with IceCube-DeepCore

DOE PAGES

Aartsen, M. G.; Abraham, K.; Ackermann, M.; ...

2016-03-30

IceCube, a gigaton-scale neutrino detector located at the South Pole, was primarily designed to search for astrophysical neutrinos with energies of PeV and higher. This goal has been achieved with the detection of the highest energy neutrinos to date. At the other end of the energy spectrum, the DeepCore extension lowers the energy threshold of the detector to approximately 10 GeV and opens the door for oscillation studies using atmospheric neutrinos. An analysis of the disappearance of these neutrinos has been completed, with the results produced being complementary with dedicated oscillation experiments. Following a review of the detector principle andmore » performance, the method used to make these calculations, as well as the results, is detailed. Finally, the future prospects of IceCube-DeepCore and the next generation of neutrino experiments at the South Pole (IceCube-Gen2, specifically the PINGU sub-detector) are briefly discussed.« less

The influence of continental ice, atmospheric CO2, and land albedo on the climate of the last glacial maximum

NASA Astrophysics Data System (ADS)

Broccoli, A. J.; Manabe, S.

1987-02-01

The contributions of expanded continental ice, reduced atmospheric CO2, and changes in land albedo to the maintenance of the climate of the last glacial maximum (LGM) are examined. A series of experiments is performed using an atmosphere-mixed layer ocean model in which these changes in boundary conditions are incorporated either singly or in combination. The model used has been shown to produce a reasonably realistic simulation of the reduced temperature of the LGM (Manabe and Broccoli 1985b). By comparing the results from pairs of experiments, the effects of each of these environmental changes can be determined. Expanded continental ice and reduced atmospheric CO2 are found to have a substantial impact on global mean temperature. The ice sheet effect is confined almost exclusively to the Northern Hemisphere, while lowered CO2 cools both hemispheres. Changes in land albedo over ice-free areas have only a minor thermal effect on a global basis. The reduction of CO2 content in the atmosphere is the primary contributor to the cooling of the Southern Hemisphere. The model sensitivity to both the ice sheet and CO2 effects is characterized by a high latitude amplification and a late autumn and early winter maximum. Substantial changes in Northern Hemisphere tropospheric circulation are found in response to LGM boundary conditions during winter. An amplified flow pattern and enhanced westerlies occur in the vicinity of the North American and Eurasian ice sheets. These alterations of the tropospheric circulation are primarily the result of the ice sheet effect, with reduced CO2 contributing only a slight amplification of the ice sheet-induced pattern.

Core/shell structure NiCo2O4@MnCo2O4 nanofibers fabricated by different temperatures for high-performance supercapacitors

NASA Astrophysics Data System (ADS)

Wang, Qing; Qin, Xuefeng; Jiang, Pengcheng; Dai, Jianfeng; Li, Weixue; Gao, Haoran

2018-03-01

Core/shell structure NiCo2O4@MnCo2O4 nanofibers (NiCo2O4@MnCo2O4 NFs) were prepared by a facile co-electrospinning method and heat treatment. The composites annealed at 500 °C have a complete, continuously obvious core/shell structure, and clear interface of composites with good morphology, while annealed at 600 °C were stacked on each other and were unable to sustain three-dimensional network structures and 700 °C calcination have completely lost one-dimensional structure. The core NiCo2O4 is about 70 nm in diameter and the MnCo2O4 shell behaves a thickness about 60 nm. When investigated as an electrode material for supercapacitors, the NiCo2O4@MnCo2O4 NFs annealed at 500 °C exihibited the specific capacitance of 463 F g-1 (0.926 F cm-2) at 1 A g-1, higher than that annealed at 600 °C 362 F g-1, 1 A g-1 (0.724 F cm-2, 1 A g-1) and 700 °C 283 F g-1, 1 A g-1 (0.566 F cm-2, 1 A g-1). These results suggest that core/shell NiCo2O4@MnCo2O4 NFs annealed at 500 °C have formed a good morphology with continuously complete core/shell structure which lead to good properties would be potential electrodes for supercapacitors.

Improved methodologies for continuous-flow analysis of stable water isotopes in ice cores

NASA Astrophysics Data System (ADS)

Jones, Tyler R.; White, James W. C.; Steig, Eric J.; Vaughn, Bruce H.; Morris, Valerie; Gkinis, Vasileios; Markle, Bradley R.; Schoenemann, Spruce W.

2017-02-01

Water isotopes in ice cores are used as a climate proxy for local temperature and regional atmospheric circulation as well as evaporative conditions in moisture source regions. Traditional measurements of water isotopes have been achieved using magnetic sector isotope ratio mass spectrometry (IRMS). However, a number of recent studies have shown that laser absorption spectrometry (LAS) performs as well or better than IRMS. The new LAS technology has been combined with continuous-flow analysis (CFA) to improve data density and sample throughput in numerous prior ice coring projects. Here, we present a comparable semi-automated LAS-CFA system for measuring high-resolution water isotopes of ice cores. We outline new methods for partitioning both system precision and mixing length into liquid and vapor components - useful measures for defining and improving the overall performance of the system. Critically, these methods take into account the uncertainty of depth registration that is not present in IRMS nor fully accounted for in other CFA studies. These analyses are achieved using samples from a South Pole firn core, a Greenland ice core, and the West Antarctic Ice Sheet (WAIS) Divide ice core. The measurement system utilizes a 16-position carousel contained in a freezer to consecutively deliver ˜ 1 m × 1.3 cm2 ice sticks to a temperature-controlled melt head, where the ice is converted to a continuous liquid stream and eventually vaporized using a concentric nebulizer for isotopic analysis. An integrated delivery system for water isotope standards is used for calibration to the Vienna Standard Mean Ocean Water (VSMOW) scale, and depth registration is achieved using a precise overhead laser distance device with an uncertainty of ±0.2 mm. As an added check on the system, we perform inter-lab LAS comparisons using WAIS Divide ice samples, a corroboratory step not taken in prior CFA studies. The overall results are important for substantiating data obtained from LAS

Laboratory IR Detection of H2O, CO2 in Ion-Irradiated Ices Relevant to Europa

NASA Technical Reports Server (NTRS)

Moore, Marla H.; Hudson, R. L.

1999-01-01

Hydrogen peroxide has been identified on Europa (Carlson et al. 1999) based in part on the 3.50 micron absorption feature observed in Galileo NIMS spectra. The observed feature was fitted with laboratory reflectance spectra of H2O + H2O2. Since condensed phase molecules on Europa (H2O, CO2, SO2, and H2O2) are bombarded with a significant flux of energetic particles (H(+), O(n+), S(n+) and e-), we examined the proton irradiation of H2O at 80 K and the conditions for the IR detection of H2O2 near 3.5 microns. Contrary to expectations, H2O2 was not detected if pure H2O ice was irradiated at 80 K. This was an unexpected result since, H2O2 was detected if pure H2O was irradiated at 18 K. We find, however, that if H2O ice contains either O2 or CO2 then H2O2 is detected after irradiation at 80 K (Moore and Hudson, 1999). The source of O2 for the H2O ice on Europa could come from surface interactions with the tenuous oxygen atmosphere, or from the bombardment of the surface by O(n+).

A method to precisely measure Ar isotopes and Xe/Kr ratios in air trapped in ice cores for simultaneous ice core dating and mean ocean temperature reconstruction

NASA Astrophysics Data System (ADS)

Yan, Y.; Ng, J.; Higgins, J. A.; Kurbatov, A.; Clifford, H.; Spaulding, N. E.; Mayewski, P. A.; Brook, E.; Bender, M. L.; Severinghaus, J. P.

2017-12-01

Antarctic efforts are underway to find and retrieve ice cores older than 800 thousand years (kyr) by both shallow drilling in "blue ice" areas and classic deep ice coring. Ice stratigraphy at "blue ice" sites is typically disordered, and the high cost of deep drilling mandates rapid reconnaissance drilling (e.g. RAID) with very small sample size. Both approaches therefore require methods of absolute dating on a single piece of ice without stratigraphic context. Here we present a dating method modified from Bender et al. (2008; PNAS) to precisely measure the isotopic composition of argon (36Ar, 38Ar, and 40Ar) in air bubbles trapped in the ice, which changes over time in a known way. Our method has an analytical uncertainty of 110 kyr (1σ) or 10% of the age of the sample, whichever is greater. We measured Ar isotopes from the Allan Hills blue ice areas, East Antarctica, where 1 Ma ice was previously found by Higgins et al. (2015; PNAS). Results show ice as old as 2.7±0.3 million years, but the ice column is stratigraphically disturbed. Hence Allan Hills ice core records should be viewed as a series of "climate snapshots" rather than a continuum. Xenon-to-krypton (Xe/Kr) ratios are also measured in the same aliquot of extracted gas to reconstruct mean ocean temperature (Shackleton et al., 2016; Fall AGU). Preliminary mean ocean temperature in ice older than 1 Ma ranges from -0.3 to -1.2 deg. colder than present with an uncertainty of 0.24 deg., which agrees well with other Pleistocene ocean temperature records (e.g. Rohling et al., 2014; Nature and Elderfield et al., 2012; Science). The observed range is 40% of the glacial-interglacial variability in the 100-kyr climate cycles ( 2 deg.), close to the 50% reduction in the glacial-interglacial δ18O amplitude across the Mid-Pleistocene Transition. Finally, Xe/Kr ratios are found to correlate positively with δD of the ice, implying a coupling between the global ocean temperature and Antarctic temperature throughout

Core drilling through the ross ice shelf (antarctica) confirmed Basal freezing.

PubMed

Zotikov, I A; Zagorodnov, V S; Raikovsky, J V

1980-03-28

New techniques that have been used to obtain a continuous ice core through the whole 416-meter thickness of the Ross Ice Shelf at Camp J-9 have demonstrated that the bottom 6 meters of the ice shelf consists of sea ice. The rate of basal freezing that is forming this ice is estimated by different methods to be 2 centimeters of ice per year. The sea ice is composed of large vertical crystals, which form the waffle-like lower boundary of the shelf. A distinct alignment of the crystals throughout the sea ice layer suggests the presence of persistent long-term currents beneath the ice shelf.

Establishing a Reliable Depth-Age Relationship for the Denali Ice Core

NASA Astrophysics Data System (ADS)

Wake, C. P.; Osterberg, E. C.; Winski, D.; Ferris, D.; Kreutz, K. J.; Introne, D.; Dalton, M.

2015-12-01

Reliable climate reconstruction from ice core records requires the development of a reliable depth-age relationship. We have established a sub-annual resolution depth-age relationship for the upper 198 meters of a 208 m ice core recovered in 2013 from Mt. Hunter (3,900 m asl), Denali National Park, central Alaska. The dating of the ice core was accomplished via annual layer counting of glaciochemical time-series combined with identification of reference horizons from volcanic eruptions and atmospheric nuclear weapons testing. Using the continuous ice core melter system at Dartmouth College, sub-seasonal samples have been collected and analyzed for major ions, liquid conductivity, particle size and concentration, and stable isotope ratios. Annual signals are apparent in several of the chemical species measured in the ice core samples. Calcium and magnesium peak in the spring, ammonium peaks in the summer, methanesulfonic acid (MSA) peaks in the autumn, and stable isotopes display a strong seasonal cycle with the most depleted values occurring during the winter. Thin ice layers representing infrequent summertime melt were also used to identify summer layers in the core. Analysis of approximately one meter sections of the core via nondestructive gamma spectrometry over depths from 84 to 124 m identified a strong radioactive cesium-137 peak at 89 m which corresponds to the 1963 layer deposited during extensive atmospheric nuclear weapons testing. Peaks in the sulfate and chloride record have been used for the preliminary identification of volcanic signals preserved in the ice core, including ten events since 1883. We are confident that the combination of robust annual layers combined with reference horizons provides a timescale for the 20th century that has an error of less than 0.5 years, making calibrations between ice core records and the instrumental climate data particularly robust. Initial annual layer counting through the entire 198 m suggests the Denali Ice

Experimental investigation of insolation-driven dust ejection from Mars' CO2 ice caps

NASA Astrophysics Data System (ADS)

Kaufmann, E.; Hagermann, A.

2017-01-01

Mars' polar caps are - depending on hemisphere and season - partially or totally covered with CO2 ice. Icy surfaces such as the polar caps of Mars behave differently from surfaces covered with rock and soil when they are irradiated by solar light. The latter absorb and reflect incoming solar radiation within a thin layer beneath the surface. In contrast, ices are partially transparent in the visible spectral range and opaque in the infrared. Due to this fact, the solar radiation can penetrate to a certain depth and raise the temperature of the ice or dust below the surface. This may play an important role in the energy balance of icy surfaces in the solar system, as already noted in previous investigations. We investigated the temperature profiles inside CO2 ice samples including a dust layer under Martian conditions. We have been able to trigger dust eruptions, but also demonstrated that these require a very narrow range of temperature and ambient pressure. We discuss possible implications for the understanding of phenomena such as arachneiform patterns or fan shaped deposits as observed in Mars' southern polar region.

Initial Continuous Chemistry Results From The Roosevelt Island Ice Core (RICE)

NASA Astrophysics Data System (ADS)

Kjær, H. A.; Vallelonga, P. T.; Simonsen, M. F.; Neff, P. D.; Bertler, N. A. N.; Svensson, A.; Dahl-Jensen, D.

2014-12-01

The Roosevelt Island ice core (79.36° S, -161.71° W) was drilled in 2011-13 at the top of the Roosevelt Island ice dome, a location surrounded by the Ross ice shelf. The RICE ice core provides a unique opportunity to look into the past evolution of the West Antarctic Ice sheet. Further the site has high accumulation; 0.26 m of ice equivalent is deposited annually allowing annual layer determination for many chemical parameters. The RICE core was drilled to bedrock and has a total length of 763 metres. Preliminary results derived from water isotopes suggest that the oldest ice reaches back to the Eemian, with the last glacial being compressed in the bottom 60 metres. We present preliminary results from the RICE ice core including continuous measurements of acidity using an optical dye method, insoluble dust particles, conductivity and calcium. The core was analyzed at the New Zealand National Ice Core Research Facility at GNS Science in Wellington. The analytical set up used to determine climate proxies in the ice core was a modified version of the Copenhagen CFA system (Bigler et al., 2011). Key volcanic layers have been matched to those from the WAIS record (Sigl et al., 2013). A significant anti-correlation between acidity and calcium was seen in the Holocene part of the record. Due to the proximity to the ocean a large fraction of the calcium originates from sea salt and is in phase with total conductivity and sodium. In combination with the insoluble dust record, calcium has been apportioned into ocean-related and dust-related sources. Variability over the Holocene is presented and attributed to changing inputs of marine and dust aerosols.

Measurements of 14C in ancient ice from Taylor Glacier, Antarctica constrain in situ cosmogenic 14CH4 and 14CO production rates

NASA Astrophysics Data System (ADS)

Petrenko, Vasilii V.; Severinghaus, Jeffrey P.; Schaefer, Hinrich; Smith, Andrew M.; Kuhl, Tanner; Baggenstos, Daniel; Hua, Quan; Brook, Edward J.; Rose, Paul; Kulin, Robb; Bauska, Thomas; Harth, Christina; Buizert, Christo; Orsi, Anais; Emanuele, Guy; Lee, James E.; Brailsford, Gordon; Keeling, Ralph; Weiss, Ray F.

2016-03-01

Carbon-14 (14C) is incorporated into glacial ice by trapping of atmospheric gases as well as direct near-surface in situ cosmogenic production. 14C of trapped methane (14CH4) is a powerful tracer for past CH4 emissions from ;old; carbon sources such as permafrost and marine CH4 clathrates. 14C in trapped carbon dioxide (14CO2) can be used for absolute dating of ice cores. In situ produced cosmogenic 14C in carbon monoxide (14CO) can potentially be used to reconstruct the past cosmic ray flux and past solar activity. Unfortunately, the trapped atmospheric and in situ cosmogenic components of 14C in glacial ice are difficult to disentangle and a thorough understanding of the in situ cosmogenic component is needed in order to extract useful information from ice core 14C. We analyzed very large (≈1000 kg) ice samples in the 2.26-19.53 m depth range from the ablation zone of Taylor Glacier, Antarctica, to study in situ cosmogenic production of 14CH4 and 14CO. All sampled ice is >50 ka in age, allowing for the assumption that most of the measured 14C originates from recent in situ cosmogenic production as ancient ice is brought to the surface via ablation. Our results place the first constraints on cosmogenic 14CH4 production rates and improve on prior estimates of 14CO production rates in ice. We find a constant 14CH4/14CO production ratio (0.0076 ± 0.0003) for samples deeper than 3 m, which allows the use of 14CO for correcting the 14CH4 signals for the in situ cosmogenic component. Our results also provide the first unambiguous confirmation of 14C production by fast muons in a natural setting (ice or rock) and suggest that the 14C production rates in ice commonly used in the literature may be too high.

Temperature reconstruction for the Tibetan Plateau in the past 2ka years from ice cores and human documentary record

NASA Astrophysics Data System (ADS)

Yang, X.

2011-12-01

Temperature variation in the past 2000 years on the plateau is reconstructed from Puruogangri ice core d18O, and compared before compositing with other three ice core records as the Dunde ice core (northeast Plateau), Guliya ice core (northwest Plateau) and Dasuopu ice core (south Plateau). The comparison reveals the synchroneity of large-scale climate events, and the composition highlights the warming in the 7th century and 12-13th centuries, and the cold in the 19th century. We searched for historical documentary about Tibet since A.D. 620, extracting record of human activities and social development directly determined or indirectly influenced by climate, and categorizing it into five aspects as basic resources, economic development, military strength, national coherence, and cultural and religious development, to quantify Tibetan development till A.D. 1900. Curve based upon the sum of the five aspects shows Tibetan national strength variation in the past 2000 years. The composited ice core record and Tibetan national strength variation shows consistency, especially during the Songtsen Gampo reign, medieval warm period and the 19th century cold period, thus suggesting the dominative role of climate change in Tibetan civilization before modern ages, as well as proposing the potential application of historical record in paleoclimate reconstruction on the Tibetan Plateau.

A Method for Continuous (239)Pu Determinations in Arctic and Antarctic Ice Cores.

PubMed

Arienzo, M M; McConnell, J R; Chellman, N; Criscitiello, A S; Curran, M; Fritzsche, D; Kipfstuhl, S; Mulvaney, R; Nolan, M; Opel, T; Sigl, M; Steffensen, J P

2016-07-05

Atmospheric nuclear weapons testing (NWT) resulted in the injection of plutonium (Pu) into the atmosphere and subsequent global deposition. We present a new method for continuous semiquantitative measurement of (239)Pu in ice cores, which was used to develop annual records of fallout from NWT in ten ice cores from Greenland and Antarctica. The (239)Pu was measured directly using an inductively coupled plasma-sector field mass spectrometer, thereby reducing analysis time and increasing depth-resolution with respect to previous methods. To validate this method, we compared our one year averaged results to published (239)Pu records and other records of NWT. The (239)Pu profiles from the Arctic ice cores reflected global trends in NWT and were in agreement with discrete Pu profiles from lower latitude ice cores. The (239)Pu measurements in the Antarctic ice cores tracked low latitude NWT, consistent with previously published discrete records from Antarctica. Advantages of the continuous (239)Pu measurement method are (1) reduced sample preparation and analysis time; (2) no requirement for additional ice samples for NWT fallout determinations; (3) measurements are exactly coregistered with all other chemical, elemental, isotopic, and gas measurements from the continuous analytical system; and (4) the long half-life means the (239)Pu record is stable through time.

Physical analysis of an Antarctic ice core-towards an integration of micro- and macrodynamics of polar ice.

PubMed

Weikusat, Ilka; Jansen, Daniela; Binder, Tobias; Eichler, Jan; Faria, Sérgio H; Wilhelms, Frank; Kipfstuhl, Sepp; Sheldon, Simon; Miller, Heinrich; Dahl-Jensen, Dorthe; Kleiner, Thomas

2017-02-13

Microstructures from deep ice cores reflect the dynamic conditions of the drill location as well as the thermodynamic history of the drill site and catchment area in great detail. Ice core parameters (crystal lattice-preferred orientation (LPO), grain size, grain shape), mesostructures (visual stratigraphy) as well as borehole deformation were measured in a deep ice core drilled at Kohnen Station, Dronning Maud Land (DML), Antarctica. These observations are used to characterize the local dynamic setting and its rheological as well as microstructural effects at the EDML ice core drilling site (European Project for Ice Coring in Antarctica in DML). The results suggest a division of the core into five distinct sections, interpreted as the effects of changing deformation boundary conditions from triaxial deformation with horizontal extension to bedrock-parallel shear. Region 1 (uppermost approx. 450 m depth) with still small macroscopic strain is dominated by compression of bubbles and strong strain and recrystallization localization. Region 2 (approx. 450-1700 m depth) shows a girdle-type LPO with the girdle plane being perpendicular to grain elongations, which indicates triaxial deformation with dominating horizontal extension. In this region (approx. 1000 m depth), the first subtle traces of shear deformation are observed in the shape-preferred orientation (SPO) by inclination of the grain elongation. Region 3 (approx. 1700-2030 m depth) represents a transitional regime between triaxial deformation and dominance of shear, which becomes apparent in the progression of the girdle to a single maximum LPO and increasing obliqueness of grain elongations. The fully developed single maximum LPO in region 4 (approx. 2030-2385 m depth) is an indicator of shear dominance. Region 5 (below approx. 2385 m depth) is marked by signs of strong shear, such as strong SPO values of grain elongation and strong kink folding of visual layers. The details of structural

Dynamic ikaite production and dissolution in sea ice - control by temperature, salinity and pCO2 conditions

NASA Astrophysics Data System (ADS)

Rysgaard, S.; Wang, F.; Galley, R. J.; Grimm, R.; Lemes, M.; Geilfus, N.-X.; Chaulk, A.; Hare, A. A.; Crabeck, O.; Else, B. G. T.; Campbell, K.; Papakyriakou, T.; Sørensen, L. L.; Sievers, J.; Notz, D.

2013-12-01

Ikaite is a hydrous calcium carbonate mineral (CaCO3 · 6H2O). It is only found in a metastable state, and decomposes rapidly once removed from near-freezing water. Recently, ikaite crystals have been found in sea ice and it has been suggested that their precipitation may play an important role in air-sea CO2 exchange in ice-covered seas. Little is known, however, of the spatial and temporal dynamics of ikaite in sea ice. Here we present evidence for highly dynamic ikaite precipitation and dissolution in sea ice grown at an out-door pool of the Sea-ice Environmental Research Facility (SERF). During the experiment, ikaite precipitated in sea ice with temperatures below -3 °C, creating three distinct zones of ikaite concentrations: (1) a mm to cm thin surface layer containing frost flowers and brine skim with bulk concentrations of > 2000 μmol kg-1, (2) an internal layer with concentrations of 200-400 μmol kg-1 and (3) a~bottom layer with concentrations of < 100 μmol kg-1. Snowfall events caused the sea ice to warm, dissolving ikaite crystals under acidic conditions. Manual removal of the snow cover allowed the sea ice to cool and brine salinities to increase, resulting in rapid ikaite precipitation. The modeled (FREZCHEM) ikaite concentrations were in the same order of magnitude as observations and suggest that ikaite concentration in sea ice increase with decreasing temperatures. Thus, varying snow conditions may play a key role in ikaite precipitation and dissolution in sea ice. This will have implications for CO2 exchange with the atmosphere and ocean.

The Radiolytic Destruction of Glycine Diluted in H2O and CO2 Ice: Implications for Mars and Other Planetary Environments

NASA Astrophysics Data System (ADS)

Gerakines, Perry A.; Hudson, R. L.

2013-10-01

Future missions to Mars and other planetary surfaces will probe under the surfaces of these worlds for signs of organic chemistry. In previous studies we have shown that glycine and other amino acids have radiolytic destruction rates that depend on temperature and on dilution within an H2O ice matrix (Gerakines et al., 2012; Gerakines and Hudson 2013). In the new work presented here, we have examined the destruction of glycine diluted in CO2 ice at various concentrations and irradiated with protons at 0.8 MeV, typical of cosmic rays and solar energetic particles. Destruction rates for glycine were measured by infrared spectroscopy in situ, without removing or warming the ice samples. New results on the half life of glycine in solid CO2 will be compared to those found in H2O ice matrices. The survivability of glycine in icy planetary surfaces rich in H2O and CO2 ice will be discussed, and the implications for planetary science missions will be considered. References: Gerakines, P. A., Hudson, R. L., Moore, M. H., and Bell, J-L. (2012). In-situ Measurements of the Radiation Stability of Amino Acids at 15 - 140 K. Icarus, 220, 647-659. Gerakines, P. A. and Hudson, R. L. (2013). Glycine's Radiolytic Destruction in Ices: First in situ Laboratory Measurements for Mars. Astrobiology, 13, 647-655.

Deep Radiostratigraphy of the East Antarctic Plateau: Connecting the Dome C and Vostok Ice Core Sites

NASA Technical Reports Server (NTRS)

Cavitte, Marie G. P.; Blankenship, Donald D.; Young, Duncan A.; Schroeder, Dustin M.; Parrenin, Frederic; Lemeur, Emmanuel; Macgregor, Joseph A.; Siegert, Martin J.

2016-01-01

Several airborne radar-sounding surveys are used to trace internal reflections around the European Project for Ice Coring in Antarctica Dome C and Vostok ice core sites. Thirteen reflections, spanning the last two glacial cycles, are traced within 200 km of Dome C, a promising region for million-year-old ice, using the University of Texas Institute for Geophysics High-Capacity Radar Sounder. This provides a dated stratigraphy to 2318 m depth at Dome C. Reflection age uncertainties are calculated from the radar range precision and signal-to-noise ratio of the internal reflections. The radar stratigraphy matches well with the Multichannel Coherent Radar Depth Sounder (MCoRDS) radar stratigraphy obtained independently. We show that radar sounding enables the extension of ice core ages through the ice sheet with an additional radar-related age uncertainty of approximately 1/3-1/2 that of the ice cores. Reflections are extended along the Byrd-Totten Glacier divide, using University of Texas/Technical University of Denmark and MCoRDS surveys. However, core-to-core connection is impeded by pervasive aeolian terranes, and Lake Vostok's influence on reflection geometry. Poor radar connection of the two ice cores is attributed to these effects and suboptimal survey design in affected areas. We demonstrate that, while ice sheet internal radar reflections are generally isochronal and can be mapped over large distances, careful survey planning is necessary to extend ice core chronologies to distant regions of the East Antarctic ice sheet.

Modeling CO 2 ice clouds with a Mars Global Climate Model

NASA Astrophysics Data System (ADS)

Audouard, Joachim; Määttänen, Anni; Listowski, Constantino; Millour, Ehouarn; Forget, Francois; Spiga, Aymeric

2016-10-01

Since the first claimed detection of CO2 ice clouds by the Mariner campaign (Herr and Pimentel, 1970), more recent observations and modelling works have put new constraints concerning their altitude, region, time and mechanisms of formation (Clancy and Sandor, 1998; Montmessin et al., 2007; Colaprete et al., 2008; Määttänen et al., 2010; Vincendon et al., 2011; Spiga et al. 2012; Listowski et al. 2014). CO2 clouds are observed at the poles at low altitudes (< 20 km) during the winter and at high altitudes (60-110 km) in the equatorial regions during the first half of the year. However, Martian CO2 clouds's variability and dynamics remain somehow elusive.Towards an understanding of Martian CO2 clouds and especially of their precise radiative impact on the climate throughout the history of the planet, including their formation and evolution in a Global Climate Model (GCM) is necessary.Adapting the CO2 clouds microphysics modeling work of Listowski et al. (2013; 2014), we aim at implementing a complete CO2 clouds scheme in the GCM of the Laboratoire de Météorologie Dynamique (LMD, Forget et al., 1999). It covers CO2 microphysics, growth, evolution and dynamics with a methodology inspired from the water ice clouds scheme recently included in the LMD GCM (Navarro et al., 2014).Two main factors control the formation and evolution of CO2 clouds in the Martian atmosphere: sufficient supersaturation of CO2 is needed and condensation nuclei must be available. Topography-induced gravity-waves (GW) are expected to propagate to the upper atmosphere where they produce cold pockets of supersaturated CO2 (Spiga et al., 2012), thus allowing the formation of clouds provided enough condensation nuclei are present. Such supersaturations have been observed by various instruments, in situ (Schofield et al., 1997) and from orbit (Montmessin et al., 2006, 2011; Forget et al., 2009).Using a GW-induced temperature profile and the 1-D version of the GCM, we simulate the formation of CO2

IceChrono v1: a probabilistic model to compute a common and optimal chronology for several ice cores

NASA Astrophysics Data System (ADS)

Parrenin, Frédéric

2015-04-01

Polar ice cores provide exceptional archives of past environmental conditions. The dating of ice cores is essential to interpret the paleo records that they contain, but it is a complicated problem since it involves different dating methods. Here I present IceChrono v1, a new probabilistic model to combine different kinds of chronological information to obtain a common and optimized chronology for several ice cores, as well as its uncertainty. It is based on the inversion of three quantities: the surface accumulation rate, the Lock-In Depth (LID) of air bubbles and the vertical thinning function. The chronological information used are: models of the sedimentation process (accumulation of snow, densification of snow into ice and air trapping, ice flow), ice and gas dated horizons, ice and gas dated depth intervals, Δdepth observations (depth shift between synchronous events recorded in the ice and in the air), stratigraphic links in between ice cores (ice-ice, air-air or mix ice-air and air-ice links). The optimization problem is formulated as a least squares problems, that is, all densities of probabilities are assumed gaussian. It is numerically solved using the Levenberg-Marquardt algorithm and a numerical evaluation of the model's Jacobian. IceChrono is similar in scope to the Datice model, but has differences from the mathematical, numerical and programming point of views. I apply IceChrono on an AICC2012-like experiment and I find similar results than Datice within a few centuries, which is a confirmation of both IceChrono and Datice codes. IceChrono v1 is freely available under the GPL v3 open source license.

Eemian interglacial reconstructed from a Greenland folded ice core.

PubMed

2013-01-24

Efforts to extract a Greenland ice core with a complete record of the Eemian interglacial (130,000 to 115,000 years ago) have until now been unsuccessful. The response of the Greenland ice sheet to the warmer-than-present climate of the Eemian has thus remained unclear. Here we present the new North Greenland Eemian Ice Drilling ('NEEM') ice core and show only a modest ice-sheet response to the strong warming in the early Eemian. We reconstructed the Eemian record from folded ice using globally homogeneous parameters known from dated Greenland and Antarctic ice-core records. On the basis of water stable isotopes, NEEM surface temperatures after the onset of the Eemian (126,000 years ago) peaked at 8 ± 4 degrees Celsius above the mean of the past millennium, followed by a gradual cooling that was probably driven by the decreasing summer insolation. Between 128,000 and 122,000 years ago, the thickness of the northwest Greenland ice sheet decreased by 400 ± 250 metres, reaching surface elevations 122,000 years ago of 130 ± 300 metres lower than the present. Extensive surface melt occurred at the NEEM site during the Eemian, a phenomenon witnessed when melt layers formed again at NEEM during the exceptional heat of July 2012. With additional warming, surface melt might become more common in the future.

Greenland ice cores tell tales on past sea level changes

NASA Astrophysics Data System (ADS)

Dahl-Jensen, D.

2017-12-01

All the deep ice cores drilled to the base of the Greenland ice sheet contain ice from the previous warm climate period, the Eemian 130-115 thousand years before present. This demonstrates the resilience of the Greenland ice sheet to a warming of 5 oC. Studies of basal material further reveal the presence of boreal forest over Greenland before ice covered Greenland. Conditions for Boreal forest implies temperatures at this time has been more than 10 oC warmer than the present. To compare the paleo-behavior of the Greenland ice sheet to the present in relation to sea level rise knowledge gabs include the reaction of ice streams to climate changes. To address this the international EGRIP-project is drilling an ice core in the center of the North East Greenland Ice Stream (NEGIS). The first results will be presented.

Continuous analysis of phosphate in a Greenland shallow ice core

NASA Astrophysics Data System (ADS)

Kjær, Helle Astrid; Svensson, Anders; Bigler, Matthias; Vallelonga, Paul; Kettner, Ernesto; Dahl-Jensen, Dorthe

2010-05-01

Phosphate is an important and sometimes limiting nutrient for primary production in the oceans. Because of deforestation and the use of phosphate as a fertilizer changes in the phosphate cycle have occurred over the last centuries. On longer time scales, sea level changes are thought to have also caused changes in the phosphate cycle. Analyzing phosphate concentrations in ice cores may help to gain important knowledge about those processes. In the present study, we attach a phosphate detection line to an existing continuous flow analysis (CFA) setup for ice core analysis at the University of Copenhagen. The CFA system is optimized for high-resolution measurements of insoluble dust particles, electrolytic melt water conductivity, and the concentrations of ammonium and sodium. For the phosphate analysis we apply a continuous and highly sensitive absorption method that has been successfully applied to determine phosphate concentrations of sea water (Zhang and Chi, 2002). A line of melt water from the CFA melt head (1.01 ml per minute) is combined with a molybdate blue reagent and an ascorbic acid buffer. An uncompleted reaction takes place in five meters of heated mixing coils before the absorption measurement at a wavelength of 710 nanometer takes place in a 2 m long liquid waveguide cell (LWCC) with an inner volume of 0.5 ml. The method has a detection limit of around 0.1 ppb and we are currently investigating a possible interference from molybdate reacting with silicates that are present in low amounts in the ice. Preliminary analysis of early Holocene samples from the NGRIP ice core show phosphate concentration values of a few ppb. In this study, we will attempt to determine past levels of phosphate in a shallow Northern Greenland firn core with an annual layer thickness of about 20 cm ice equivalent. With a melt speed of 2.5 cm ice per minute our method should allow the resolution of any seasonal variability in phosphate concentrations.

Geographic Distribution of N2, CH4, CO2, and H2O Ices on Triton from Near-IR Spectroscopic Monitoring

NASA Astrophysics Data System (ADS)

Grundy, W. M.; Young, L. A.; Young, E. F.; Buie, M. W.; Spencer, J. R.

2004-11-01

We present new 0.8 to 2.4 μ m spectral observations of Neptune's satellite Triton, obtained at IRTF\\slash SpeX between 2001 and 2004 as part of an ongoing search for time-variable phenomena associated with Triton's seasonal volatile transport processes, and also perhaps with reported shorter-term "reddening" events. The ability to detect spectral changes on these time scales depends critically on accurate characterization of any cyclic variations resulting from Triton's 5.877 day rotation period. We will report on our observations of periodic variations of Triton's near-IR absorption bands of N2, CH4, and H2O ices, but not of CO2 ice, in this initial stage of our Triton monitoring program. The observed variations (or lack thereof) give an indication of how these four ice species are distributed in longitude. The most heterogeneously distributed ice is N2, which shows nearly twice as much absorption on Triton's Neptune-facing hemisphere as on the anti-Neptune hemisphere. Comparison with Voyager-era, visual wavelength imaging of Triton's surface suggest that the observed N2 ice is concentrated on low-latitude regions of Triton's polar cap, which are predominantly located on the Neptune-facing hemisphere. Non-volatile H2O ice seems to be slightly concentrated on Triton's leading hemisphere. Despite being highly diluted in N2 ice, the longitudinal distribution of Triton's CH4 ice differs from that of Triton's N2 ice, being slightly concentrated on Triton's trailing hemisphere. Triton's CO2 ice shows the least longitudinal variation, suggesting that it is either very uniformly distributed or that it is confined to high latitudes. This work was supported by NASA's Planetary Astronomy and Planetary Geology &\\ Geophysics programs, and by NSF's Planetary Astronomy program. \\hangindent=0.3truein Grundy, W.M., and L.A. Young (2004) Near infrared spectral monitoring of Triton with IRTF\\slash SpeX I: Establishing a baseline. Icarus (in press).

The 2140 cm(exp -1) (4.673 Microns) Solid CO Band: The Case for Interstellar O2 and N2 and the Photochemistry of Non-Polar Interstellar Ice Analogs

NASA Technical Reports Server (NTRS)

Elsila, Jamie; Allamandola, Louis J.; Sandford, Scott A.; Witteborn, Fred C. (Technical Monitor)

1996-01-01

The infrared spectra of CO frozen in non-polar ices containing N2, CO2, O2, and H2O, and the ultraviolet photochemistry of these interstellar/precometary ice analogs are reported. The spectra are used to test the hypothesis that the narrow 2140/cm (4.673 micrometer) interstellar absorption feature attributed to solid CO might be produced by CO frozen in ices containing non-polar species such as N2 and O2. It is shown that mixed molecular ices containing CO, N2, O2, and CO2 provide a very good match to the interstellar band at all temperatures between 12 and 30 K both before and after photolysis. The optical constants (real and imaginary parts of the index of refraction) in the region of the solid CO feature are reported for several of these ices.

SHARAD Finds Voluminous CO2 Ice Sequestered in the Martian South Polar Layered Deposits

NASA Astrophysics Data System (ADS)

Phillips, R. J.; Davis, B. J.; Byrne, S.; Campbell, B. A.; Carter, L. M.; Haberle, R. M.; Holt, J. W.; Kahre, M. A.; Nunes, D. C.; Plaut, J. J.; Putzig, N. E.; Smith, I. B.; Smrekar, S. E.; Tanaka, K. L.; Titus, T. N.

2010-12-01

The SHARAD instrument on the Mars Reconnaissance Orbiter (MRO) mission has carried out systematic radar soundings of the layered deposits at both martian polar regions. While well-organized sets of radar reflectors are ubiquitous in the North Polar Layered Deposits, those in the South Polar Layered Deposits (SPLD) are limited to specific regions, and it is difficult to map SPLD-wide radar stratigraphy. What is evident in the radar observations are four regional reflection-free zones (RFZ) distinguished qualitatively by their radar characteristics. They are up to a kilometer in thickness and extend downward from near the surface. One such zone (RFZ3) occurs beneath the South Polar Residual Cap (SPRC), which is composed of ~5 m of solid CO2 underlain by an apparently thin layer of water ice. Using a correlation technique, we inverted for the real permittivity, ɛ', on each of 41 usable SHARAD orbits over RFZ3. The results were mean values of ɛ' = 2.0 or 2.1, with a σ of 0.2. A secondary technique based on the “smoothest” solution gave similar results. These values are exceptionally close to the laboratory-measured permittivity value of bulk CO2 ice [Pettinelli et al., 2003] and distant from the bulk water ice value (ɛ' = 3.15); water ice is the dominant volatile in the SPLD. An alternative hypothesis for ɛ' = 2.0-2.1 is that the RFZ3 material is porous water ice, but this can be strongly discounted based on theoretical and empirical models of ɛ' of porous water ice vs. thickness. By the same arguments, the proposed CO2 material also cannot be very porous, and ɛ' should be close to the bulk value. With the permittivity estimates, radar time delays were converted to depth, and for RFZ3 a mean thickness of 210-220 m and a volume of 4,200-4,400 km3 result. This is unlikely to be the entire volume because MRO’s orbital inclination precludes SHARAD sounding poleward of ~87°S, where RFZ3 appears to extend. We do find a very good spatial correlation of RFZ3 with

Spatially-controlled NiCo2O4@MnO2 core-shell nanoarray with hollow NiCo2O4 cores and MnO2 flake shells: an efficient catalyst for oxygen evolution reaction.

PubMed

Xue, Hairong; Yu, Hongjie; Li, Yinghao; Deng, Kai; Xu, You; Li, Xiaonian; Wang, Hongjing; Wang, Liang

2018-07-13

Control of structures and components of the nanoarray catalysts is very important for electrochemical energy conversion. Herein, unique NiCo 2 O 4 @MnO 2 core-shell nanoarray with hollow NiCo 2 O 4 Cores and MnO 2 flake shells is in situ fabricated on carbon textile via a two-step hydrothermal treatment followed by a subsequent annealing. The as-made nanoarray is highly active and durable catalyst for oxygen evolution reaction in alkaline media attribute to the synergetic effect derived from spatially separated nanoarray with favorable NiCo 2 O 4 and MnO 2 compositions.

The condensation and vaporization behavior of ices containing SO2, H2S, and CO2 - Implications for Io

NASA Astrophysics Data System (ADS)

Sandford, Scott A.; Allamandola, Louis J.

1993-12-01

The present compilation of measurements of the physical and IR spectral properties of ices whose molecular compositions are relevant to the case of Io encompasses ice systems containing SO2, H2S, and CO2. Surface-binding energies used to calculate the residence times of molecules on a surface as a function of temperature furnish crucially important parameters for models attending to the transport of such molecules to the surface of Io. The values thus derived show that SO2 frosts anneal rapidly.

Chronology of Pu isotopes and 236U in an Arctic ice core.

PubMed

Wendel, C C; Oughton, D H; Lind, O C; Skipperud, L; Fifield, L K; Isaksson, E; Tims, S G; Salbu, B

2013-09-01

In the present work, state of the art isotopic fingerprinting techniques are applied to an Arctic ice core in order to quantify deposition of U and Pu, and to identify possible tropospheric transport of debris from former Soviet Union test sites Semipalatinsk (Central Asia) and Novaya Zemlya (Arctic Ocean). An ice core chronology of (236)U, (239)Pu, and (240)Pu concentrations, and atom ratios, measured by accelerator mass spectrometry in a 28.6m deep ice core from the Austfonna glacier at Nordaustlandet, Svalbard is presented. The ice core chronology corresponds to the period 1949 to 1999. The main sources of Pu and (236)U contamination in the Arctic were the atmospheric nuclear detonations in the period 1945 to 1980, as global fallout, and tropospheric fallout from the former Soviet Union test sites Novaya Zemlya and Semipalatinsk. Activity concentrations of (239+240)Pu ranged from 0.008 to 0.254 mBq cm(-2) and (236)U from 0.0039 to 0.053 μBq cm(-2). Concentrations varied in concordance with (137)Cs concentrations in the same ice core. In contrast to previous published results, the concentrations of Pu and (236)U were found to be higher at depths corresponding to the pre-moratorium period (1949 to 1959) than to the post-moratorium period (1961 and 1962). The (240)Pu/(239)Pu ratio ranged from 0.15 to 0.19, and (236)U/(239)Pu ranged from 0.18 to 1.4. The Pu atom ratios ranged within the limits of global fallout in the most intensive period of nuclear atmospheric testing (1952 to 1962). To the best knowledge of the authors the present work is the first publication on biogeochemical cycles with respect to (236)U concentrations and (236)U/(239)Pu atom ratios in the Arctic and in ice cores. Copyright © 2013 Elsevier B.V. All rights reserved.

Ice Mapping Observations in Galactic Star-Forming Regions: the AKARI Legacy

NASA Astrophysics Data System (ADS)

Fraser, Helen Jane; Suutarinnen, Aleksi; Noble, Jennifer

2015-08-01

It is becoming increasingly clear that explaining the small-scale distribution of many gas-phase molecules relies on our interpretation of the complex inter-connectivity between gas- and solid-phase interstellar chemistries. Inputs to proto-stellar astrochemical models are required that exploit ice compositions reflecting the historical physical conditions in pre-stellar environments when the ices first formed. Such data are required to translate the near-universe picture of ice-composition to our understanding of the role of extra-galactic ices in star-formation at higher redshifts.Here we present the first attempts at multi-object ice detections, and the subsequent ice column density mapping. The AKARI space telescope was uniquely capable of observing all the ice features between 2 and 5 microns, thereby detecting H2O, CO and CO2 ices concurrently, through their stretching vibrational features. Our group has successfully extracted an unprecedented volume of ice spectra from AKARI, including sources with not more than 2 mJy flux at 3 microns, showing:(a) H2O CO and CO2 ices on 30 lines of sight towards pre-stellar and star-forming cores, which when combined with laboratory experiments indicate how the chemistries of these three ices are interlinked (Noble et al (2013)),(b) ice maps showing the spatial distribution of water ice across 12 pre-stellar cores, in different molecular clouds (Suutarinnen et al (2015)), and the distribution of ice components within these cores on 1000 AU scales (Noble et al (2015)),(c) over 200 new detections of water ice, mostly on lines of sight towards background sources (> 145), indicating that water ice column density has a minimum value as a function of Av, but on a cloud-by-cloud basis typically correlates with Av, and dust emissivity at 250 microns (Suutarinnen et al (2015)),(d) the first detections of HDO ice towards background stars (Fraser et al (2015)).We discuss whether these results support the picture of a generic chemical

Taxonomic characterization and the bio-potential of bacteria isolated from glacier ice cores in the High Arctic.

PubMed

Singh, Purnima; Singh, Shiv Mohan; Roy, Utpal

2016-03-01

Glacier ice and firn cores have ecological and biotechnological importance. The present study is aimed at characterizing bacteria in crustal ice cores from Svalbard, the Arctic. Counts of viable isolates ranged from 10 to 7000 CFU/ml (mean 803 CFU/ml) while the total bacterial numbers ranged from 7.20 × 10(4) to 2.59 × 10(7)  cells ml(-1) (mean 3.12 × 10(6)  cells ml(-1) ). Based on 16S rDNA sequence data, the identified species belonged to seven species, namely Bacillus barbaricus, Pseudomonas orientalis, Pseudomonas oryzihabitans, Pseudomonas fluorescens, Pseudomonas syncyanea, Sphingomonas dokdonensis, and Sphingomonas phyllosphaerae, with a sequence similarity ranging between 93.5 and 99.9% with taxa present in the database. The isolates exhibited unique phenotypic properties, and three isolates (MLB-2, MLB-5, and MLB-9) are novel species, yet to be described. To the best of our knowledge, this is the first report on characterization of cultured bacterial communities from Svalbard ice cores. We conclude that high lipase, protease, cellulase, amylase, and urease activities expressed by most of the isolates provide a clue to the potential industrial applications of these organisms. These microbes, producing cold-adapted enzymes may provide an opportunity for biotechnological research. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Remote-Raman and Micro-Raman Studies of Solid CO2, CH4, Gas Hydrates and Ice

NASA Technical Reports Server (NTRS)

Sharma, S. K.; Misra, A. K.; Lucey, P. G.; Exarhos, G. J.; Windisch, C. F., Jr.

2004-01-01

It is well known that on Mars CO2 is the principal constituent of the thin atmosphere and on a seasonal basis CO2 snow and frost coats the polar caps. Also over 25% of the Martian atmosphere freezes out and sublimes again each year. The Mars Odyssey Emission Imaging system (THEMIS) has discovered water ice exposed near the edge of Mars southern perennials cap. In recent years, it has been suggested that in Martian subsurface CO2 may exist as gas hydrate (8CO2 + 44 H2O) with melting temperature of 10C. Since the crust of Mars has been stable for enough time there is also a possibility that methane formed by magmatic processes and/or as a byproduct of anaerobic deep biosphere activity to have raised toward the planet s surface. This methane would have been captured and stored as methane hydrate, which concentrates methane and water. Determination of abundance and distribution of these ices on the surface and in the near surface are of fundamental importance for understanding Martian atmosphere, and for future exploration of Mars. In this work, we have evaluated feasibility of using remote Raman and micro-Raman spectroscopy as potential nondestructive and non-contact techniques for detecting solid CO2, CH4 gas, and gas hydrates as well as water-ice on planetary surfaces.

Brief communication: ikaite (CaCO3*6H2O) discovered in Arctic sea ice

NASA Astrophysics Data System (ADS)

Dieckmann, G. S.; Nehrke, G.; Uhlig, C.; Göttlicher, J.; Gerland, S.; Granskog, M. A.; Thomas, D. N.

2010-02-01

We report for the first time on the discovery of calcium carbonate crystals as ikaite (CaCO3*6H2O) in sea ice from the Arctic (Kongsfjorden, Svalbard). This finding demonstrates that the precipitation of calcium carbonate during the freezing of sea ice is not restricted to the Antarctic, where it was observed for the first time in 2008. This finding is an important step in the quest to quantify its impact on the sea ice driven carbon cycle and should in the future enable improvement parametrization sea ice carbon models.

CO2 Ice Formation and CO2 Gas Depletion in the Polar Winter Atmosphere of Mars from Mars Climate Sounder Measurements

NASA Astrophysics Data System (ADS)

Kleinboehl, A.; Patel, P. K.; Schofield, J. T.; Kass, D. M.; Hayne, P. O.; McCleese, D. J.

2016-12-01

Temperatures in the martian lower atmosphere commonly reach the frost point of CO2 in the polar winter vortices over an extended vertical range. New retrievals from the Mars Climate Sounder (MCS) instrument on Mars Reconnaissance Orbiter allow the characterization of the winter polar regions with improved accuracy. MCS is a passive infrared sounder with 5 mid-infrared, 3 far infrared, and one broadband visible/near-infrared channels. Each spectral channel uses a linear detector array consisting of 21 elements, which provides -10 to 90 km altitude coverage when pointed at the Mars limb. From the infrared measurements, vertical profiles of temperature and aerosols are retrieved with an altitude resolution of about 5 km. Due to their long optical path through the atmosphere, limb measurements are susceptible to horizontal gradients in temperature or absorber amount in their line-of-sight, an effect that is particularly important in polar winter regions due to strong latitudinal temperature gradients in the atmosphere. The new retrievals take horizontal gradients in temperature and aerosols into account by means of a two-dimensional radiative transfer scheme. The resulting temperature profiles reveal that temperatures in the south winter polar region repeatedly drop several degrees below the frost point of CO2. This behavior is consistent with the removal of CO2 from the atmosphere through condensation, resulting in an atmosphere that is depleted in gaseous CO2 and enhanced in non-condensable gases like N2 and Ar. In these regions emission features at 22 μm are often found in MCS limb measurements, consistent with the presence of CO2 ice in the polar vortex. We will map these depletions of CO2 gas and show correlations with the occurrence of CO2 ice. We will provide comparisons of these effects between the southern and the northern polar winter vortices.

Isotopic composition of ice cores and meltwater from upper fremont glacier and Galena Creek rock glacier, Wyoming

USGS Publications Warehouse

DeWayne, Cecil L.; Green, J.R.; Vogt, S.; Michel, R.; Cottrell, G.

1998-01-01

Meltwater runoff from glaciers can result from various sources, including recent precipitation and melted glacial ice. Determining the origin of the meltwater from glaciers through isotopic analysis can provide information about such things as the character and distribution of ablation on glaciers. A 9.4 m ice core and meltwater were collected in 1995 and 1996 at the glacigenic Galena Creek rock glacier in Wyoming's Absaroka Mountains. Measurements of chlorine-36 (36Cl), tritium (3H), sulphur-35 (35S), and delta oxygen-18 (??18O) were compared to similar measurements from an ice core taken from the Upper Fremont Glacier in the Wind River Range of Wyoming collected in 1991-95. Meltwater samples from three sites on the rock glacier yielded 36Cl concentrations that ranged from 2.1 ?? 1.0 X 106 to 5.8??0.3 X 106 atoms/l. The ice-core 36Cl concentrations from Galena Creek ranged from 3.4??0.3 X 105 to 1.0??0.1 X 106 atoms/l. Analysis of an ice core from the Upper Fremont Glacier yielded 36Cl concentrations of 1.2??0.2 X 106 and 5.2??0.2 X 106 atoms/l for pre- 1940 ice and between 2 X 106 and 3 X 106 atoms/l for post-1980 ice. Purdue's PRIME Lab analyzed the ice from the Upper Fremont Glacier. The highest concentration of 36Cl in the ice was 77 ?? 2 X 106 atoms/l and was deposited during the peak of atmospheric nuclear weapons testing in the late 1950s. This is an order of magnitude greater than the largest measured concentration from both the Upper Fremont Glacier ice core that was not affected by weapons testing fallout and the ice core collected from the Galena Creek rock glacier. Tritium concentrations from the rock glacier ranged from 9.2??0.6 to 13.2??0.8 tritium units (TU) in the meltwater to -1.3??1.3 TU in the ice core. Concentrations of 3H in the Upper Fremont Glacier ice core ranged from 0 TU in the ice older than 50 years to 6-12 TU in the ice deposited in the last 10 years. The maximum 3H concentration in ice from the Upper Fremont Glacier deposited in the

Tree ring and ice core time scales around the Santorini eruption

NASA Astrophysics Data System (ADS)

Löfroth, Elin; Muscheler, Raimund; Aldahan, Ala; Possnert, Göran; Berggren, Ann-Marie

2010-05-01

When studying cosmogenic radionuclides in ice core and tree ring archives around the Santorini eruption a ~20 year discrepancy was found between the records (Muscheler 2009). In this study a new 10Be dataset from the NGRIP ice core is presented. It has a resolution of 7 years and spans the period 3752-3244 BP (1803-1295 BC). The NGRIP 10Be record and the previously published 10Be GRIP record were compared to the IntCal datasets to further investigate the discrepancy between the ice core and tree ring chronologies. By modelling the 14C production rate based on atmospheric 14C records a comparison could be made to the 10Be flux which is assumed to represent the 10Be production rate. This showed a time shift of ~23 years between the records. The sensitivity of the results to changes in important model parameters was evaluated. Uncertainties in the carbon cycle model cannot explain a substantial part of the timing differences. Potential influences of climate and atmospheric processes on the 10Be deposition were studied using δ18O from the respective cores and GISP2 ice core ion data. The comparison to δ18O revealed a small but significant correlation between 10Be flux and δ18O when the 14C-derived production signal was removed from the 10Be curves. The ion data, as proxies for atmospheric circulation changes, did not show any correlations to the 10Be record or the 10Be/14C difference. When including possible data uncertainties there is still a minimum discrepancy of ~10 years between the 10Be ice core and the 14C tree ring record. Due to lack of alternative explanations it is concluded that the ice core and/or the tree ring chronologies contains unaccounted errors in this range. This also reconciles the radiocarbon 1627-1600 BC (Friedrich et al., 2006) and ice core 1642±5 BC (Vinther et al., 2006) datings of the Santorini eruption. Friedrich, W.L., Kromer, B., Friedrich, M., Heinemeier, J., Pfeiffer, T., & Talamo, S., 2006: Santorini eruption radiocarbon dated to

Automated Laser-Light Scattering measurements of Impurities, Bubbles, and Imperfections in Ice Cores

NASA Astrophysics Data System (ADS)

Stolz, M. R.; Ram, M.

2004-12-01

Laser- light scattering (LLS) on polar ice, or on polar ice meltwater, is an accepted method for measuring the concentration of water insoluble aerosol deposits (dust) in the ice. LLS on polar ice can also be used to measure water soluble aerosols, as well as imperfections (air bubbles and cavities) in the ice. LLS was originally proposed by Hammer (1977a, b) as a method for measuring the dust concentration in polar ice meltwater. Ram et al. (1995) later advanced the method and applied it to solid ice, measuring the dust concentration profile along the deep, bubble-free sections of the Greenland Ice Sheet Projetct 2 (GISP2) ice core (Ram et al., 1995, 2000) from central Greenland. In this paper, we will put previous empirical findings (Ram et al., 1995, 2000) on a theoretical footing, and extend the usability of LLS on ice into the realm of the non-transparent, bubbly polar ice. For LLS on clear, bubble-free polar ice, we studied numerically the scattering of light by soluble and insoluble (dust) aerosol particles embedded in the ice to complement previous experimental studies (Ram et al., 2000). For air bubbles in polar ice, we calculated the effects of multiple light scattering using Mie theory and Monte Carlo simulations, and found a method for determining the bubble number size and concentration using LLS on bubbly ice. We also demonstrated that LLS can be used on bubbly ice to measure annual layers rapidly in an objective manner. Hammer, C. U. (1977a), Dating of Greenland ice cores by microparticle concentration analyses., in International Symposium on Isotopes and Impurities in Snow and Ice, pp. 297-301, IAHS publ. no. 118. Hammer, C. U. (1977b), Dust studies on Greenland ice cores, in International Symposium on Isotopes and Impurities in Snow and Ice, pp. 365-370, IAHS publ. no. 118. Ram, M., M. Illing, P. Weber, G. Koenig, and M. Kaplan (1995), Polar ice stratigraphy from laser-light scattering: Scattering from ice, Geophys. Res. Lett., 22(24), 3525

Atmospheric CO2 variations on millennial-scale during MIS 6

NASA Astrophysics Data System (ADS)

Shin, Jinhwa; Grilli, Roberto; Chappellaz, Jérôme; Teste, Grégory; Nehrbass-Ahles, Christoph; Schmidely, Loïc; Schmitt, Jochen; Stocker, Thomas; Fischer, Hubertus

2017-04-01

Understanding natural carbon cycle / climate feedbacks on various time scales is highly important for predicting future climate changes. Paleoclimate records of Antarctic temperatures, relative sea level and foraminiferal isotope and pollen records in sediment cores from the Portuguese margin have shown climate variations on millennial time scale over the Marine Isotope Stage 6 (MIS 6; from approximately 135 to 190 kyr BP). These proxy data suggested iceberg calving in the North Atlantic result in cooling in the Northern hemisphere and warming in Antarctica by changes in the Atlantic Meridional Overturning Circulation, which is explained by a bipolar see-saw trend in the ocean (Margari et al., 2010). Atmospheric CO2 reconstruction from Antarctic ice cores can provide key information on how atmospheric CO2 concentrations are linked to millennial-scale climate changes. However, existing CO2 records cannot be used to address this relationship because of the lack of suitable temporal resolution. In this work, we will present a new CO2 record with an improved time resolution, obtained from the Dome C ice core (75˚ 06'S, 123˚ 24'E) spanning the MIS 6 period, using dry extraction methods. We will examine millennial-scale features in atmospheric CO2, and their possible links with other proxies covering MIS 6. Margari, V., Skinner, L. C., Tzedakis, P. C., Ganopolski, A., Vautravers, M., and Shackleton, N. J.: The nature of millennial scale climate variability during the past two glacial periods, Nat.Geosci., 3, 127-131, 2010.

Quantification of ikaite in Antarctic sea ice

NASA Astrophysics Data System (ADS)

Fischer, M.; Thomas, D. N.; Krell, A.; Nehrke, G.; Göttlicher, J.; Norman, L.; Riaux-Gobin, C.; Dieckmann, G. S.

2012-02-01

Calcium carbonate precipitation in sea ice can increase pCO2 during precipitation in winter and decrease pCO2 during dissolution in spring. CaCO3 precipitation in sea ice is thought to potentially drive significant CO2 uptake by the ocean. However, little is known about the quantitative spatial and temporal distribution of CaCO3 within sea ice. This is the first quantitative study of hydrous calcium carbonate, as ikaite, in sea ice and discusses its potential significance for the carbon cycle in polar oceans. Ice cores and brine samples were collected from pack and land fast sea ice between September and December 2007 during an expedition in the East Antarctic and another off Terre Adélie, Antarctica. Samples were analysed for CaCO3, Salinity, DOC, DON, Phosphate, and total alkalinity. A relationship between the measured parameters and CaCO3 precipitation could not be observed. We found calcium carbonate, as ikaite, mostly in the top layer of sea ice with values up to 126 mg ikaite per liter melted sea ice. This potentially represents a contribution between 0.12 and 9 Tg C to the annual carbon flux in polar oceans. The horizontal distribution of ikaite in sea ice was heterogenous. We also found the precipitate in the snow on top of the sea ice.

Ice cores and SeaRISE: What we do (and don't) know

NASA Technical Reports Server (NTRS)

Alley, Richard B.

1991-01-01

Ice core analyses are needed in SeaRISE to learn what the West Antarctic ice sheet and other marine ice sheets were like in the past, what climate changes led to their present states, and how they behave. The major results of interest to SeaRISE from previous ice core analyses in West Antarctic are that the end of the last ice age caused temperature and accumulation rate increases in inland regions, leading to ice sheet thickening followed by thinning to the present.

An automated approach for annual layer counting in ice cores

NASA Astrophysics Data System (ADS)

Winstrup, M.; Svensson, A.; Rasmussen, S. O.; Winther, O.; Steig, E.; Axelrod, A.

2012-04-01

The temporal resolution of some ice cores is sufficient to preserve seasonal information in the ice core record. In such cases, annual layer counting represents one of the most accurate methods to produce a chronology for the core. Yet, manual layer counting is a tedious and sometimes ambiguous job. As reliable layer recognition becomes more difficult, a manual approach increasingly relies on human interpretation of the available data. Thus, much may be gained by an automated and therefore objective approach for annual layer identification in ice cores. We have developed a novel method for automated annual layer counting in ice cores, which relies on Bayesian statistics. It uses algorithms from the statistical framework of Hidden Markov Models (HMM), originally developed for use in machine speech recognition. The strength of this layer detection algorithm lies in the way it is able to imitate the manual procedures for annual layer counting, while being based on purely objective criteria for annual layer identification. With this methodology, it is possible to determine the most likely position of multiple layer boundaries in an entire section of ice core data at once. It provides a probabilistic uncertainty estimate of the resulting layer count, hence ensuring a proper treatment of ambiguous layer boundaries in the data. Furthermore multiple data series can be incorporated to be used at once, hence allowing for a full multi-parameter annual layer counting method similar to a manual approach. In this study, the automated layer counting algorithm has been applied to data from the NGRIP ice core, Greenland. The NGRIP ice core has very high temporal resolution with depth, and hence the potential to be dated by annual layer counting far back in time. In previous studies [Andersen et al., 2006; Svensson et al., 2008], manual layer counting has been carried out back to 60 kyr BP. A comparison between the counted annual layers based on the two approaches will be presented

"Self-preservation" of CO(2) gas hydrates--surface microstructure and ice perfection.

PubMed

Falenty, Andrzej; Kuhs, Werner F

2009-12-10

Gas hydrates can exhibit an anomalously slow decomposition outside their thermodynamic stability field; the phenomenon is called "self-preservation" and is mostly studied at ambient pressure and at temperatures between approximately 240 K and the melting point of ice. Here, we present a combination of in situ neutron diffraction studies, pVT work, and ex situ scanning electron microscopy (SEM) on CO(2) clathrates covering a much broader p-T field, stretching from 200 to 270 K and pressures between the hydrate stability limit and 0.6 kPa (6 mbar), a pressure far outside stability. The self-preservation regime above 240 K is confirmed over a broad pressure range and appears to be caused by the annealing of an ice cover formed in the initial hydrate decomposition. Another, previously unknown regime of the self-preservation exists below this temperature, extending however only over a rather narrow pressure range. In this case, the initial ice microstructure is dominated by a fast two-dimensional growth covering rapidly the clathrate surface. All observations lend strong support to the idea that the phenomenon of self-preservation is linked to the permeability of the ice cover governed by (1) the initial microstructure of ice and/or (2) the subsequent annealing of this ice coating. The interplay of the microstructure of newly formed ice and its annealing with the ongoing decomposition reaction leads to various decomposition paths and under certain conditions to a very pronounced preservation anomaly.

Revisiting the Scattering Greenhouse Effect of CO2 Ice Clouds

NASA Astrophysics Data System (ADS)

Kitzmann, D.

2016-02-01

Carbon dioxide ice clouds are thought to play an important role for cold terrestrial planets with thick CO2 dominated atmospheres. Various previous studies showed that a scattering greenhouse effect by carbon dioxide ice clouds could result in a massive warming of the planetary surface. However, all of these studies only employed simplified two-stream radiative transfer schemes to describe the anisotropic scattering. Using accurate radiative transfer models with a general discrete ordinate method, this study revisits this important effect and shows that the positive climatic impact of carbon dioxide clouds was strongly overestimated in the past. The revised scattering greenhouse effect can have important implications for the early Mars, but also for planets like the early Earth or the position of the outer boundary of the habitable zone.

Application of composite flow laws to grain size distributions derived from polar ice cores

NASA Astrophysics Data System (ADS)

Binder, Tobias; de Bresser, Hans; Jansen, Daniela; Weikusat, Ilka; Garbe, Christoph; Kipfstuhl, Sepp

2014-05-01

Apart from evaluating the crystallographic orientation, focus of microstructural analysis of natural ice during the last decades has been to create depth-profiles of mean grain size. Several ice flow models incorporated mean grain size as a variable. Although such a mean value may coincide well with the size of a large proportion of the grains, smaller/larger grains are effectively ignored. These smaller/larger grains, however, may affect the ice flow modeling. Variability in grain size is observed on centimeter, meter and kilometer scale along deep polar ice cores. Composite flow laws allow considering the effect of this variability on rheology, by weighing the contribution of grain-size-sensitive (GSS, diffusion/grain boundary sliding) and grain-size-insensitive (GSI, dislocation) creep mechanisms taking the full grain size distribution into account [1]. Extraction of hundreds of grain size distributions for different depths along an ice core has become relatively easy by automatic image processing techniques [2]. The shallow ice approximation is widely adopted in ice sheet modeling and approaches the full-Stokes solution for small ratios of vertical to horizontal characteristic dimensions. In this approximation shear stress in the vertical plain dominates the strain. This assumption is not applicable at ice divides or dome structures, where most deep ice core drilling sites are located. Within the upper two thirds of the ice column longitudinal stresses are not negligible and ice deformation is dominated by vertical strain. The Dansgaard-Johnsen model [3] predicts a dominating, constant vertical strain rate for the upper two thirds of the ice sheet, whereas in the lower ice column vertical shear becomes the main driver for ice deformation. We derived vertical strain rates from the upper NEEM ice core (North-West Greenland) and compared them to classical estimates of strain rates at the NEEM site. Assuming intervals of constant accumulation rates, we found a

Low pCO2 under sea-ice melt in the Canada Basin of the western Arctic Ocean

NASA Astrophysics Data System (ADS)

Kosugi, Naohiro; Sasano, Daisuke; Ishii, Masao; Nishino, Shigeto; Uchida, Hiroshi; Yoshikawa-Inoue, Hisayuki

2017-12-01

In September 2013, we observed an expanse of surface water with low CO2 partial pressure (pCO2sea) (< 200 µatm) in the Chukchi Sea of the western Arctic Ocean. The large undersaturation of CO2 in this region was the result of massive primary production after the sea-ice retreat in June and July. In the surface of the Canada Basin, salinity was low (< 27) and pCO2sea was closer to the air-sea CO2 equilibrium (˜ 360 µatm). From the relationships between salinity and total alkalinity, we confirmed that the low salinity in the Canada Basin was due to the larger fraction of meltwater input (˜ 0.16) rather than the riverine discharge (˜ 0.1). Such an increase in pCO2sea was not so clear in the coastal region near Point Barrow, where the fraction of riverine discharge was larger than that of sea-ice melt. We also identified low pCO2sea (< 250 µatm) in the depth of 30-50 m under the halocline of the Canada Basin. This subsurface low pCO2sea was attributed to the advection of Pacific-origin water, in which dissolved inorganic carbon is relatively low, through the Chukchi Sea where net primary production is high. Oxygen supersaturation (> 20 µmol kg-1) in the subsurface low pCO2sea layer in the Canada Basin indicated significant net primary production undersea and/or in preformed condition. If these low pCO2sea layers surface by wind mixing, they will act as additional CO2 sinks; however, this is unlikely because intensification of stratification by sea-ice melt inhibits mixing across the halocline.

Laboratory measurements of heterogeneous CO2 ice nucleation on nanoparticles under conditions relevant to the Martian mesosphere

NASA Astrophysics Data System (ADS)

Nachbar, Mario; Duft, Denis; Mangan, Thomas Peter; Martin, Juan Carlos Gomez; Plane, John M. C.; Leisner, Thomas

2016-05-01

Clouds of CO2 ice particles have been observed in the Martian mesosphere. These clouds are believed to be formed through heterogeneous nucleation of CO2 on nanometer-sized meteoric smoke particles (MSPs) or upward propagated Martian dust particles (MDPs). Large uncertainties still exist in parameterizing the microphysical formation process of these clouds as key physicochemical parameters are not well known. We present measurements on the nucleation and growth of CO2 ice on sub-4 nm radius iron oxide and silica particles representing MSPs at conditions close to the mesosphere of Mars. For both particle materials we determine the desorption energy of CO2 to be ΔFdes = (18.5 ± 0.2) kJ mol-1 corresponding to ΔFdes = (0.192 ± 0.002) eV and obtain m = 0.78 ± 0.02 for the contact parameter that governs heterogeneous nucleation by analyzing the measurements using classical heterogeneous nucleation theory. We did not find any temperature dependence for the contact parameter in the temperature range examined (64 K to 73 K). By applying these values for MSPs in the Martian mesosphere, we derive characteristic temperatures for the onset of CO2 ice nucleation, which are 8-18 K below the CO2 frost point temperature, depending on particle size. This is in line with the occurrence of highly supersaturated conditions extending to 20 K below frost point temperature without the observation of clouds. Moreover, the sticking coefficient of CO2 on solid CO2 was determined to be near unity. We further argue that the same parameters can be applied to CO2 nucleation on upward propagated MDPs.

Earth's Climate History from Glaciers and Ice Cores

NASA Astrophysics Data System (ADS)

Thompson, Lonnie

2013-03-01

Glaciers serve both as recorders and early indicators of climate change. Over the past 35 years our research team has recovered climatic and environmental histories from ice cores drilled in both Polar Regions and from low to mid-latitude, high-elevation ice fields. Those ice core -derived proxy records extending back 25,000 years have made it possible to compare glacial stage conditions in the Tropics with those in the Polar Regions. High-resolution records of δ18O (in part a temperature proxy) demonstrate that the current warming at high elevations in the mid- to lower latitudes is unprecedented for the last two millennia, although at many sites the early Holocene was warmer than today. Remarkable similarities between changes in the highland and coastal cultures of Peru and regional climate variability, especially precipitation, imply a strong connection between prehistoric human activities and regional climate. Ice cores retrieved from shrinking glaciers around the world confirm their continuous existence for periods ranging from hundreds to thousands of years, suggesting that current climatological conditions in those regions today are different from those under which these ice fields originated and have been sustained. The ongoing widespread melting of high-elevation glaciers and ice caps, particularly in low to middle latitudes, provides strong evidence that a large-scale, pervasive and, in some cases, rapid change in Earth's climate system is underway. Observations of glacier shrinkage during the 20th and 21st century girdle the globe from the South American Andes, the Himalayas, Kilimanjaro (Tanzania, Africa) and glaciers near Puncak Jaya, Indonesia (New Guinea). The history and fate of these ice caps, told through the adventure, beauty and the scientific evidence from some of world's most remote mountain tops, provide a global perspective for contemporary climate. NSF Paleoclimate Program

Timing of insolation forcing, CO2 and sea level changes around the current and last four interglacial periods

NASA Astrophysics Data System (ADS)

Kawamura, K.; Aoki, S.; Nakazawa, T.; Abe-Ouchi, A.; Saito, F.

2013-12-01

Investigation of the roles of different forcings (e.g. orbital variations and greenhouse gases) on climate and sea level requires a paleoclimate chronology with high accuracy. Such a chronology for the past 360 ky was constructed through orbital tuning of O2/N2 ratio of trapped air in the Dome Fuji and Vostok ice cores with local summer insolation (Kawamura et al., 2007). We extend the O2/N2 chronology back to ~500 kyr by analyzing the second Dome Fuji ice core, and find the duration of 11 ka, 5 ka, 9 ka, and 20 ka for MIS 5e, 7e, 9e and 11c interglacial periods in Antarctica, with similar variations in atmospheric CO2. The termination timings are consistent with the rising phase of Northern Hemisphere summer insolation. Marine sediment cores from northern North Atlantic contain millennial-scale signatures in various proxy records (e.g. SST, IRD), including abrupt climatic shifts and bipolar seesaw. Based on the bipolar correlation of millennial-scale events, it is possible to transfer our accurate chronology to marine cores from the North Atlantic. As a first attempt, we correlate the planktonic δ18O and IRD records from the marine core ODP 980 with the ice-core δ18O and CH4 around MIS 11. We find that the durations of interglacial plateaus of planktonic δ18O (proxy for sea surface environments) and benthic δ18O (proxy for ice volume and deep-sea temperature) for MIS 11c are 20 and 15 ka, respectively, which are significantly shorter than originally suggested. These durations are similar to that of Antarctic climate and atmospheric CO2. However, the onsets of interglacial levels in ODP980 for MIS 11 are significantly later than those in Antarctic δ18O and atmospheric CO2 (by as much as ~10 ka), suggesting very long duration (more than one precession cycle) for the complete deglaciation and northern high-latitude warming for Termination V. Atmospheric CO2 may have been the critical forcing for this termination. The long duration of Termination V is consistent

Continuous methane measurements from a late Holocene Greenland ice core: Atmospheric and in-situ signals

NASA Astrophysics Data System (ADS)

Rhodes, Rachael H.; Faïn, Xavier; Stowasser, Christopher; Blunier, Thomas; Chappellaz, Jérôme; McConnell, Joseph R.; Romanini, Daniele; Mitchell, Logan E.; Brook, Edward J.

2013-04-01

Ancient air trapped inside bubbles in ice cores can now be analysed for methane concentration utilising a laser spectrometer coupled to a continuous melter system. We present a new ultra-high resolution record of atmospheric methane variability over the last 1800 yr obtained from continuous analysis of a shallow ice core from the North Greenland Eemian project (NEEM-2011-S1) during a 4-week laboratory-based measurement campaign. Our record faithfully replicates the form and amplitudes of multi-decadal oscillations previously observed in other ice cores and demonstrates the detailed depth resolution (5.3 cm), rapid acquisition time (30 m day-1) and good long-term reproducibility (2.6%, 2σ) of the continuous measurement technique. In addition, we report the detection of high frequency ice core methane signals of non-atmospheric origin. Firstly, measurements of air from the firn-ice transition region and an interval of ice core dating from 1546-1560 AD (gas age) resolve apparently quasi-annual scale methane oscillations. Traditional gas chromatography measurements on discrete ice samples confirm these signals and indicate peak-to-peak amplitudes of ca. 22 parts per billion (ppb). We hypothesise that these oscillations result from staggered bubble close-off between seasonal layers of contrasting density during time periods of sustained multi-year atmospheric methane change. Secondly, we report the detection of abrupt (20-100 cm depth interval), high amplitude (35-80 ppb excess) methane spikes in the NEEM ice that are reproduced by discrete measurements. We show for the first time that methane spikes present in thin and infrequent layers in polar, glacial ice are accompanied by elevated concentrations of carbon- and nitrogen-based chemical impurities, and suggest that biological in-situ production may be responsible.

Electron Irradiation of Kuiper Belt Surface Ices: Ternary N2-CH4-CO Mixtures as a Case Study

NASA Astrophysics Data System (ADS)

Kim, Y. S.; Kaiser, R. I.

2012-10-01

The space weathering of icy Kuiper Belt Objects was investigated in this case study by exposing methane (CH4) and carbon monoxide (CO) doped nitrogen (N2) ices at 10 K to ionizing radiation in the form of energetic electrons. Online and in situ Fourier transform infrared spectroscopy was utilized to monitor the radiation-induced chemical processing of these ices. Along with isocyanic acid (HNCO), the products could be mainly derived from those formed in irradiated binary ices of the N2-CH4 and CO-CH4 systems: nitrogen-bearing products were found in the form of hydrogen cyanide (HCN), hydrogen isocyanide (HNC), diazomethane (CH2N2), and its radical fragment (HCN2); oxygen-bearing products were of acetaldehyde (CH3CHO), formyl radical (HCO), and formaldehyde (H2CO). As in the pure ices, the methyl radical (CH3) and ethane (C2H6) were also detected, as were carbon dioxide (CO2) and the azide radical (N3). Based on the temporal evolution of the newly formed products, kinetic reaction schemes were then developed to fit the temporal profiles of the newly formed species, resulting in numerical sets of rate constants. The current study highlights important constraints on the preferential formation of isocyanic acid (HNCO) over hydrogen cyanide (HCN) and hydrogen isocyanide (HNC), thus guiding the astrobiological and chemical evolution of those distant bodies.

Antarctic ice core samples: culturable bacterial diversity.

PubMed

Shivaji, Sisinthy; Begum, Zareena; Shiva Nageswara Rao, Singireesu Soma; Vishnu Vardhan Reddy, Puram V; Manasa, Poorna; Sailaja, Buddi; Prathiba, Mambatta S; Thamban, Meloth; Krishnan, Kottekkatu P; Singh, Shiv M; Srinivas, Tanuku N R

2013-01-01

Culturable bacterial abundance at 11 different depths of a 50.26 m ice core from the Tallaksenvarden Nunatak, Antarctica, varied from 0.02 to 5.8 × 10(3) CFU ml(-1) of the melt water. A total of 138 bacterial strains were recovered from the 11 different depths of the ice core. Based on 16S rRNA gene sequence analyses, the 138 isolates could be categorized into 25 phylotypes belonging to phyla Actinobacteria, Bacteroidetes, Firmicutes and Proteobacteria. All isolates had 16S rRNA sequences similar to previously determined sequences (97.2-100%). No correlation was observed in the distribution of the isolates at the various depths either at the phylum, genus or species level. The 25 phylotypes varied in growth temperature range, tolerance to NaCl, growth pH range and ability to produce eight different extracellular enzymes at either 4 or 18 °C. Iso-, anteiso-, unsaturated and saturated fatty acids together constituted a significant proportion of the total fatty acid composition. Copyright © 2012 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.

The 1500m South Pole Ice Core: Recovering a 40 Ka Environmental Record

NASA Technical Reports Server (NTRS)

Casey, Kimberly Ann; Neumann, Thomas Allen; Fudge, T. J.; Neumann, T. A.; Steig, E. J.; Cavitte, M. G. P.; Blankenship, D. D.

2014-01-01

Supported by the US National Science Foundation, a new 1500 m, approximately 40 ka old ice core will be recovered from South Pole during the 2014/15 and 2015/16 austral summer seasons using the new US Intermediate Depth Drill. The combination of low temperatures, relatively high accumulation rates and low impurity concentrations at South Pole will yield detailed records of ice chemistry and trace atmospheric gases. The South Pole ice core will provide a climate history record of a unique area of the East Antarctic plateau that is partly influenced by weather systems that cross the West Antarctic ice sheet. The ice at South Pole flows at approximately 10m a(exp-1) and the South Pole ice-core site is a significant distance from an ice divide. Therefore, ice recovered at depth originated progressively farther upstream of the coring site. New ground-penetrating radar collected over the drill site location shows no anthropogenic influence over the past approximately 50 years or upper 15 m. Depth-age scale modeling results show consistent and plausible annual-layer thicknesses and accumulation rate histories, indicating that no significant stratigraphic disturbances exist in the upper 1500m near the ice-core drill site.

Glycine formation in CO2:CH4:NH3 ices induced by 0-70 eV electrons

NASA Astrophysics Data System (ADS)

Esmaili, Sasan; Bass, Andrew D.; Cloutier, Pierre; Sanche, Léon; Huels, Michael A.

2018-04-01

Glycine (Gly), the simplest amino-acid building-block of proteins, has been identified on icy dust grains in the interstellar medium, icy comets, and ice covered meteorites. These astrophysical ices contain simple molecules (e.g., CO2, H2O, CH4, HCN, and NH3) and are exposed to complex radiation fields, e.g., UV, γ, or X-rays, stellar/solar wind particles, or cosmic rays. While much current effort is focused on understanding the radiochemistry induced in these ices by high energy radiation, the effects of the abundant secondary low energy electrons (LEEs) it produces have been mostly assumed rather than studied. Here we present the results for the exposure of multilayer CO2:CH4:NH3 ice mixtures to 0-70 eV electrons under simulated astrophysical conditions. Mass selected temperature programmed desorption (TPD) of our electron irradiated films reveals multiple products, most notably intact glycine, which is supported by control measurements of both irradiated or un-irradiated binary mixture films, and un-irradiated CO2:CH4:NH3 ices spiked with Gly. The threshold of Gly formation by LEEs is near 9 eV, while the TPD analysis of Gly film growth allows us to determine the "quantum" yield for 70 eV electrons to be about 0.004 Gly per incident electron. Our results show that simple amino acids can be formed directly from simple molecular ingredients, none of which possess preformed C—C or C—N bonds, by the copious secondary LEEs that are generated by ionizing radiation in astrophysical ices.

Glycine formation in CO2:CH4:NH3 ices induced by 0-70 eV electrons.

PubMed

Esmaili, Sasan; Bass, Andrew D; Cloutier, Pierre; Sanche, Léon; Huels, Michael A

2018-04-28

Glycine (Gly), the simplest amino-acid building-block of proteins, has been identified on icy dust grains in the interstellar medium, icy comets, and ice covered meteorites. These astrophysical ices contain simple molecules (e.g., CO 2 , H 2 O, CH 4 , HCN, and NH 3 ) and are exposed to complex radiation fields, e.g., UV, γ, or X-rays, stellar/solar wind particles, or cosmic rays. While much current effort is focused on understanding the radiochemistry induced in these ices by high energy radiation, the effects of the abundant secondary low energy electrons (LEEs) it produces have been mostly assumed rather than studied. Here we present the results for the exposure of multilayer CO 2 :CH 4 :NH 3 ice mixtures to 0-70 eV electrons under simulated astrophysical conditions. Mass selected temperature programmed desorption (TPD) of our electron irradiated films reveals multiple products, most notably intact glycine, which is supported by control measurements of both irradiated or un-irradiated binary mixture films, and un-irradiated CO 2 :CH 4 :NH 3 ices spiked with Gly. The threshold of Gly formation by LEEs is near 9 eV, while the TPD analysis of Gly film growth allows us to determine the "quantum" yield for 70 eV electrons to be about 0.004 Gly per incident electron. Our results show that simple amino acids can be formed directly from simple molecular ingredients, none of which possess preformed C-C or C-N bonds, by the copious secondary LEEs that are generated by ionizing radiation in astrophysical ices.

Critical Fracture Toughness Measurements of an Antarctic Ice Core

NASA Astrophysics Data System (ADS)

Christmann, Julia; Müller, Ralf; Webber, Kyle; Isaia, Daniel; Schader, Florian; Kippstuhl, Sepp; Freitag, Johannes; Humbert, Angelika

2014-05-01

Fracture toughness is a material parameter describing the resistance of a pre-existing defect in a body to further crack extension. The fracture toughness of glacial ice as a function of density is important for modeling efforts aspire to predict calving behavior. In the presented experiments this fracture toughness is measured using an ice core from Kohnen Station, Dronning Maud Land, Antarctica. The samples were sawed in an ice lab at the Alfred Wegener Institute in Bremerhaven at -20°C and had the dimensions of standard test samples with thickness 14 mm, width 28 mm and length 126 mm. The samples originate from a depth of 94.6 m to 96 m. The grain size of the samples was also identified. The grain size was found to be rather uniform. The critical fracture toughness is determined in a four-point bending approach using single edge V-notch beam samples. The initial notch length was around 2.5 mm and was prepared using a drilling machine. The experimental setup was designed at the Institute of Materials Science at Darmstadt. In this setup the force increases linearly, until the maximum force is reached, where the specific sample fractures. This procedure was done in an ice lab with a temperature of -15°C. The equations to calculate the fracture toughness for pure bending are derived from an elastic stress analysis and are given as a standard test method to detect the fracture toughness. An X-ray computer tomography (CT scanner) was used to determine the ice core densities. The tests cover densities from 843 kg m-3 to 871 kg m-3. Thereby the influence of the fracture toughness on the density was analyzed and compared to previous investigations of this material parameter. Finally the dependence of the measured toughness on thickness, width, and position in the core cross-section was investigated.

Arrival of Sulfate Aerosols from Iceland's Laki Eruption (1783-1784 AD) to the Greenland Ice Sheet: A Critical Ice Core Dating Tool

NASA Astrophysics Data System (ADS)

Wei, L.; Mosley-Thompson, E.

2006-12-01

The Laki (Iceland) volcanic event was a basaltic flood lava eruption lasting from June 8, 1783 to February 7, 1784. The timing of the arrival of the sulfate aerosols and volcanic fragments to the Greenland Ice Sheet (GIS) remains uncertain, but is important to confirm as the highly conductive sulfate layer has been consistently used as a time stratigraphic marker (1783 AD) in ice cores collected across Greenland. However, in the GISP2 ice core a few glass shards were found within the annual layer lying just below that containing the sulfate aerosols from Laki suggesting that the ash arrived first, in 1783, while the aerosols arrived the following year [Fiacco et al., 1994]. Additional published ice core results have neither confirmed nor refuted this observation. We have taken advantage of the accurately dated, high temporal resolution ice cores collected by PARCA (Program for Arctic Regional Climate Assessment) to (1) determine more precisely the timing of the arrival of Laki's sulfate aerosols and (2) assess the spatial variability of the excess sulfate contributed by Laki to the GIS. Our results indicate that the sulfate emitted from the Laki eruption most likely arrived on the GIS in the late summer or early fall of 1783 AD. This is also supported by contemporary weather logs and official reports of the appearance of Laki haze [Thordarson and Self, 2003]. The flux of Laki sulfate varies significantly over the GIS, largely as a function of the regional annual accumulation rate. Laki sulfate aerosols also arrived as a single pulse in most of the PARCA cores, suggesting that only a small fraction of the gases emitted from Laki reached the stratosphere. References: Fiacco, R.J.,et al., Atmospheric aerosol loading and transport due to the 1783-84 Laki eruption in Iceland, interpreted from ash particles and acidity in the GISP2 ice core, Quat. Res., 42, 231-240, 1994. Thordarson, T, and S. Self, Atmospheric and environmental effects of the 1783-1784 Laki eruption: A

Ice cores and calcite precipitates from alpine ice caves as useful proxies in paleoclimate reconstructions

NASA Astrophysics Data System (ADS)

Colucci, Renato R.; Barbante, Carlo; Bertò, Michele; Dreossi, Giuliano; Festi, Daniela; Forte, Emanuele; Gabrieli, Jacopo; Guglielmin, Mauro; Lenaz, Davide; Luetscher, Marc; Maggi, Valter; Princivalle, Francesco; Schwikowski, Margit; Stenni, Barbara; Žebre, Manja

2017-04-01

In the last years a growing set of research campaigns have been undertaken in the European southeastern Alps. The aim of such interest is mainly due to the peculiar climatic conditions of this area, allowing the existence of periglacial and glacial evidence at the lowest altitude in the Alps. The reason for such "anomaly" is likely ascribable to very high mean annual precipitation and local topoclimatic amplifications. In the frame of this research, in the fall 2013 a 7.8 m long ice-core has been extracted from a permanent cave ice deposit located in the area of Mt. Canin (2,587 masl) in the Julian Alps. The ice-core has been cut and analysed in terms of: a) oxygen and hydrogen isotope composition; b); black carbon and dust concentrations; c) water conductivity; d) mineralogical analyses via X-ray powder diffraction. In the fall 2016, in the same area, a set of 1.0 m long horizontal ice cores have been extracted in another ice cave deposit, intercepting a preserved layer of coarse cryogenic cave carbonates (CCCcoarse). Such original finding represents the first alpine evidence of in situ CCCcoarse and the first occurrence from the southern side of the Alps. A unique opportunity to better understand the processes associated with the formation of CCCcoarse and the well-preserved status of samples allow planning, besides U/Th datings, several different analyses which may be associated with the precipitation of CCC. Subglacial calcite crusts, widespread in the area, represents a further proxy able to help understanding the evolution of climate during the holocene in this alpine sector. In the light of accelerated climate change we discuss here the potential of this still untapped and fragile cryospheric archives for paleoclimatic reconstructions in high elevated areas of the Alps.

The Late Holocene Atmospheric Methane Budget Reconstructed from Ice Cores

NASA Astrophysics Data System (ADS)

Mitchell, Logan E.

In this thesis I used a newly developed methane measurement line to make high-resolution, high-precision measurements of methane during the late Holocene (2800 years BP to present). This new measurement line is capable of an analytical precision of < 3 ppb using ˜120 g samples. The reduced sample size requirements as well as automation of a significant portion of the analysis process have enabled me to make >1500 discrete ice core methane measurements and construct the highest resolution records of methane available over the late Holocene. I first used a shallow ice core from WAIS Divide (WDC05A) to produce a 1000 year long methane record with a ˜9 year temporal resolution. This record confirmed the existence of multidecadal scale variations that were first observed in the Law Dome, Antarctica ice core. I then explored a range of paleoclimate archives for possible mechanistic connections with methane concentrations on multidecadal timescales. In addition, I present a detailed description of the analytical methods used to obtain high-precision measurements of methane including the effects of solubility and a new chronology for the WDC05A ice core. I found that, in general, the correlations with paleoclimate proxies for temperature and precipitation were low over a range of geographic regions. Of these, the highest correlations were found from 1400-1600 C.E. during the onset of the Little Ice Age and with a drought index in the headwater region of the major East Asian rivers. Large population losses in Asia and the Americas are also coincident with methane concentration decreases indicating that anthropogenic activities may have been impacting multidecadal scale methane variability. In the second component I extended the WAIS Divide record back to 2800 years B.P. and also measured methane from GISP2D over this time interval. These records allowed me to examine the methane Inter-Polar Difference (IPD) which is created by greater northern hemispheric sources. The IPD

Historical Isotopic Temperature Record from the Vostok Ice Core (420,000 years BP-present)

DOE Data Explorer

Petit, J. R. [Laboratoire de Glaciogie et Geophysique de l'Environnement; Raynaud, D. [Laboratoire de Glaciogie et Geophysique de l'Environnement; Lorius, C. [Laboratoire de Glaciogie et Geophysique de l'Environnement; Jouzel, J. [Laboratoire des Sciences du Climat et de l'Environnement; Delaygue, G. [Laboratoire des Sciences du Climat et de l'Environnement; Barkov, N. I. [Arctic and Antarctic Research Inst. (AARI), St. Petersburg (Russian Federation); Kotlyakov, V. M. [Institute of Geography, Russia

2000-01-01

Because isotopic fractions of the heavier oxygen-18 (18O) and deuterium (D) in snowfall are temperature-dependent and a strong spatial correlation exists between the annual mean temperature and the mean isotopic ratio (18O or δD) of precipitation, it is possible to derive ice-core climate records. The record presented by Jouzel et al. (1987) was the first ice core record to span a full glacial-interglacial cycle. That record was based on an ice core drilled at the Russian Vostok station in central east Antarctica. The 2083-m ice core was obtained during a series of drillings in the early 1970s and 1980s and was the result of collaboration between French and former-Soviet scientists. Drilling continued at Vostok and was completed in January 1998, reaching a depth of 3623 m, the deepest ice core ever recovered (Petit et al. 1997, 1999). The resulting core allows the ice core record of climate properties at Vostok to be extended to ~420 kyr BP.

36Cl, 10Be and 26Al analyses from the GISP2 bedrock core and the stability of the Greenland Ice Sheet

NASA Astrophysics Data System (ADS)

Schaefer, J. M.; Finkel, R. C.; Fifield, L. K.; Balco, G.; Caffee, M.; Alley, R. B.; Briner, J. P.; Young, N. E.; Gow, A. J.; Schwartz, R.

2017-12-01

The Greenland Ice Sheet (GIS) contains the equivalent of 7.4 meters (24 feet) of global sea-level rise. Its stability in our warming climate is therefore a pressing concern. However, the scarcity of proxy evidence of the palaeo-stability of the GIS means that its history remains controversial (for example 1 vs. 2). Current model simulations of the past GIS configuration during warm periods remain ambiguous but do show that both the magnitude and the duration of warmth are critical to ice-sheet stability. Much of this uncertainty reflects the fact that the direct evidence, if it exists, is buried beneath the present ice sheet. Here we attempt to overcome this obstacle via cosmogenic nuclide analysis of sub-GIS bedrock. Cosmogenic nuclides directly monitor periods of surface exposure to cosmic ray bombardment and thus ice-free conditions, and the ratios between cosmogenic nuclides of differing half-lives are diagnostic for periods the GIS shielded the bedrock. We focus on the bedrock underneath the 3042 m long GISP2 ice core, retrieved in 1993, and recently published the 10Be (half-life 1.4 Myr) and 26Al (half-life 0.7 Myr) analyses from quartz of this bedrock core 3. The published results show that Greenland was nearly ice-free for extended periods during the Pleistocene (2.6 Myr -11.7 kyr ago) and narrow the spectrum of possible GIS histories: the longest period of stability of the present ice sheet that is consistent with the 10Be and 26Al measurements is 1.1 Myr, assuming that this was preceded by more than 280 kyr of ice-free conditions. More dynamic scenarios, in which Greenland was ice-free during any or all Pleistocene interglacials, would be also consistent with the 10Be and 26Al data. We now present 36Cl (half-life 0.3 Myr) data from feldspars separated from this bedrock core. The measured 36Cl depth profile is consistent with the 10Be and 26Al data, indicating that most of the analyzed 36Cl was produced by neutron spallation during periods of nearly ice

State dependence of climatic instability over the past 720,000 years from Antarctic ice cores and climate modeling.

PubMed

Kawamura, Kenji; Abe-Ouchi, Ayako; Motoyama, Hideaki; Ageta, Yutaka; Aoki, Shuji; Azuma, Nobuhiko; Fujii, Yoshiyuki; Fujita, Koji; Fujita, Shuji; Fukui, Kotaro; Furukawa, Teruo; Furusaki, Atsushi; Goto-Azuma, Kumiko; Greve, Ralf; Hirabayashi, Motohiro; Hondoh, Takeo; Hori, Akira; Horikawa, Shinichiro; Horiuchi, Kazuho; Igarashi, Makoto; Iizuka, Yoshinori; Kameda, Takao; Kanda, Hiroshi; Kohno, Mika; Kuramoto, Takayuki; Matsushi, Yuki; Miyahara, Morihiro; Miyake, Takayuki; Miyamoto, Atsushi; Nagashima, Yasuo; Nakayama, Yoshiki; Nakazawa, Takakiyo; Nakazawa, Fumio; Nishio, Fumihiko; Obinata, Ichio; Ohgaito, Rumi; Oka, Akira; Okuno, Jun'ichi; Okuyama, Junichi; Oyabu, Ikumi; Parrenin, Frédéric; Pattyn, Frank; Saito, Fuyuki; Saito, Takashi; Saito, Takeshi; Sakurai, Toshimitsu; Sasa, Kimikazu; Seddik, Hakime; Shibata, Yasuyuki; Shinbori, Kunio; Suzuki, Keisuke; Suzuki, Toshitaka; Takahashi, Akiyoshi; Takahashi, Kunio; Takahashi, Shuhei; Takata, Morimasa; Tanaka, Yoichi; Uemura, Ryu; Watanabe, Genta; Watanabe, Okitsugu; Yamasaki, Tetsuhide; Yokoyama, Kotaro; Yoshimori, Masakazu; Yoshimoto, Takayasu

2017-02-01

Climatic variabilities on millennial and longer time scales with a bipolar seesaw pattern have been documented in paleoclimatic records, but their frequencies, relationships with mean climatic state, and mechanisms remain unclear. Understanding the processes and sensitivities that underlie these changes will underpin better understanding of the climate system and projections of its future change. We investigate the long-term characteristics of climatic variability using a new ice-core record from Dome Fuji, East Antarctica, combined with an existing long record from the Dome C ice core. Antarctic warming events over the past 720,000 years are most frequent when the Antarctic temperature is slightly below average on orbital time scales, equivalent to an intermediate climate during glacial periods, whereas interglacial and fully glaciated climates are unfavourable for a millennial-scale bipolar seesaw. Numerical experiments using a fully coupled atmosphere-ocean general circulation model with freshwater hosing in the northern North Atlantic showed that climate becomes most unstable in intermediate glacial conditions associated with large changes in sea ice and the Atlantic Meridional Overturning Circulation. Model sensitivity experiments suggest that the prerequisite for the most frequent climate instability with bipolar seesaw pattern during the late Pleistocene era is associated with reduced atmospheric CO 2 concentration via global cooling and sea ice formation in the North Atlantic, in addition to extended Northern Hemisphere ice sheets.

State dependence of climatic instability over the past 720,000 years from Antarctic ice cores and climate modeling

PubMed Central

Kawamura, Kenji; Abe-Ouchi, Ayako; Motoyama, Hideaki; Ageta, Yutaka; Aoki, Shuji; Azuma, Nobuhiko; Fujii, Yoshiyuki; Fujita, Koji; Fujita, Shuji; Fukui, Kotaro; Furukawa, Teruo; Furusaki, Atsushi; Goto-Azuma, Kumiko; Greve, Ralf; Hirabayashi, Motohiro; Hondoh, Takeo; Hori, Akira; Horikawa, Shinichiro; Horiuchi, Kazuho; Igarashi, Makoto; Iizuka, Yoshinori; Kameda, Takao; Kanda, Hiroshi; Kohno, Mika; Kuramoto, Takayuki; Matsushi, Yuki; Miyahara, Morihiro; Miyake, Takayuki; Miyamoto, Atsushi; Nagashima, Yasuo; Nakayama, Yoshiki; Nakazawa, Takakiyo; Nakazawa, Fumio; Nishio, Fumihiko; Obinata, Ichio; Ohgaito, Rumi; Oka, Akira; Okuno, Jun’ichi; Okuyama, Junichi; Oyabu, Ikumi; Parrenin, Frédéric; Pattyn, Frank; Saito, Fuyuki; Saito, Takashi; Saito, Takeshi; Sakurai, Toshimitsu; Sasa, Kimikazu; Seddik, Hakime; Shibata, Yasuyuki; Shinbori, Kunio; Suzuki, Keisuke; Suzuki, Toshitaka; Takahashi, Akiyoshi; Takahashi, Kunio; Takahashi, Shuhei; Takata, Morimasa; Tanaka, Yoichi; Uemura, Ryu; Watanabe, Genta; Watanabe, Okitsugu; Yamasaki, Tetsuhide; Yokoyama, Kotaro; Yoshimori, Masakazu; Yoshimoto, Takayasu

2017-01-01

Climatic variabilities on millennial and longer time scales with a bipolar seesaw pattern have been documented in paleoclimatic records, but their frequencies, relationships with mean climatic state, and mechanisms remain unclear. Understanding the processes and sensitivities that underlie these changes will underpin better understanding of the climate system and projections of its future change. We investigate the long-term characteristics of climatic variability using a new ice-core record from Dome Fuji, East Antarctica, combined with an existing long record from the Dome C ice core. Antarctic warming events over the past 720,000 years are most frequent when the Antarctic temperature is slightly below average on orbital time scales, equivalent to an intermediate climate during glacial periods, whereas interglacial and fully glaciated climates are unfavourable for a millennial-scale bipolar seesaw. Numerical experiments using a fully coupled atmosphere-ocean general circulation model with freshwater hosing in the northern North Atlantic showed that climate becomes most unstable in intermediate glacial conditions associated with large changes in sea ice and the Atlantic Meridional Overturning Circulation. Model sensitivity experiments suggest that the prerequisite for the most frequent climate instability with bipolar seesaw pattern during the late Pleistocene era is associated with reduced atmospheric CO2 concentration via global cooling and sea ice formation in the North Atlantic, in addition to extended Northern Hemisphere ice sheets. PMID:28246631

Carbonaceous aerosol tracers in ice-cores record multi-decadal climate oscillations

PubMed Central

Seki, Osamu; Kawamura, Kimitaka; Bendle, James A. P.; Izawa, Yusuke; Suzuki, Ikuko; Shiraiwa, Takayuki; Fujii, Yoshiyuki

2015-01-01

Carbonaceous aerosols influence the climate via direct and indirect effects on radiative balance. However, the factors controlling the emissions, transport and role of carbonaceous aerosols in the climate system are highly uncertain. Here we investigate organic tracers in ice cores from Greenland and Kamchatka and find that, throughout the period covered by the records (1550 to 2000 CE), the concentrations and composition of biomass burning-, soil bacterial- and plant wax- tracers correspond to Arctic and regional temperatures as well as the warm season Arctic Oscillation (AO) over multi-decadal time-scales. Specifically, order of magnitude decreases (increases) in abundances of ice-core organic tracers, likely representing significant decreases (increases) in the atmospheric loading of carbonaceous aerosols, occur during colder (warmer) phases in the high latitudinal Northern Hemisphere. This raises questions about causality and possible carbonaceous aerosol feedback mechanisms. Our work opens new avenues for ice core research. Translating concentrations of organic tracers (μg/kg-ice or TOC) from ice-cores, into estimates of the atmospheric loading of carbonaceous aerosols (μg/m3) combined with new model constraints on the strength and sign of climate forcing by carbonaceous aerosols should be a priority for future research. PMID:26411576

Dating of 30m ice cores drilled by Japanese Antarctic Research Expedition and environmental change study

NASA Astrophysics Data System (ADS)

Motoyama, H.; Suzuki, T.; Fukui, K.; Ohno, H.; Hoshina, Y.; Hirabayashi, M.; Fujita, S.

2017-12-01

1. Introduction It is possible to reveal the past climate and environmental change from the ice core drilled in polar ice sheet and glaciers. The 54th Japanese Antarctic Research Expedition conducted several shallow core drillings up to 30 m depth in the inland and coastal areas of the East Antarctic ice sheet. Ice core sample was cut out at a thickness of about 5 cm in the cold room of the National Institute of Polar Research, and analyzed ion, water isotope, dust and so one. We also conducted dielectric profile measurement (DEP measurement). The age as a key layer of large-scale volcanic explosion was based on Sigl et al. (Nature Climate Change, 2014). 2. Inland ice core Ice cores were collected at the NDF site (77°47'14"S, 39°03'34"E, 3754 m.a.s.l.) and S80 site (80°00'00"S, 40°30'04"E, 3622 m.a.s.l.). Dating of ice core was done as follows. Calculate water equivalent from core density. Accumulate water equivalent from the surface. Approximate the relation of depth - cumulative water equivalent by a quartic equation. We determined the key layer with nssSO42 - peak corresponding to several large volcanic explosions. The accumulation rate was kept constant between the key layers. As a result, NDF was estimated to be around 1360 AD and S80 was estimated to be around 1400 AD in the deepest ice core. 3. Coastal ice core An ice core was collected at coastal H15 sites (69°04'10"S, 40°44'51"E, 1030 m.a.s.l.). Dating of ice core was done as follows. Calculate water equivalent from ice core density. Accumulate water equivalent from the surface. Approximate the relation of depth - cumulative water equivalent by a quartic equation. Basically we decided to summer (December) and winter (June) due to the seasonal change of the water isotope (δD or δ18O). In addition to the seasonal change of isotope, confirm the following. Maximum of SO42- / Na +, which is earlier in time than the maximum of water isotope. Maximum of MSA at about the same time as the maximum of the

Marine biological controls on atmospheric CO2 and climate

NASA Technical Reports Server (NTRS)

Mcelroy, M. B.

1983-01-01

It is argued that the ocean is losing N gas faster than N is being returned to the ocean, and that replenishment of the N supply in the ocean usually occurs during ice ages. Available N from river and estruarine transport and from rainfall after formation by lightning are shown to be at a rate too low to compensate for the 10,000 yr oceanic lifetime of N. Ice sheets advance and transfer moraine N to the ocean, lower the sea levels, erode the ocean beds, promote greater biological productivity, and reduce CO2. Ice core samples have indicated a variability in the atmospheric N content that could be attributed to the ice age scenario.

Eastern Ross Ice Sheet Deglacial History inferred from the Roosevelt Island Ice Core

NASA Astrophysics Data System (ADS)

Fudge, T. J.; Buizert, C.; Lee, J.; Waddington, E. D.; Bertler, N. A. N.; Conway, H.; Brook, E.; Severinghaus, J. P.

2017-12-01

The Ross Ice Sheet drains large portions of both West and East Antarctica. Understanding the retreat of the Ross Ice Sheet following the Last Glacial Maximum is particularly difficult in the eastern Ross area where there is no exposed rock and the Ross Ice Shelf prevents extensive bathymetric mapping. Coastal domes, by preserving old ice, can be used to infer the establishment of grounded ice and be used to infer past ice thickness. Here we focus on Roosevelt Island, in the eastern Ross Sea, where the Roosevelt Island Climate Evolution project recently completed an ice core to bedrock. Using ice-flow modeling constrained by the depth-age relationship and an independent estimate of accumulation rate from firn-densification measurements and modeling, we infer ice thickness histories for the LGM (20ka) to present. Preliminary results indicate thinning of 300m between 15ka and 12ka is required. This is similar to the amount and timing of thinning inferred at Siple Dome, in the central Ross Sea (Waddington et al., 2005; Price et al., 2007) and supports the presence of active ice streams throughout the Ross Ice Sheet advance during the LGM.

Physical properties of the WAIS Divide ice core

USGS Publications Warehouse

Fitzpatrick, Joan J.; Voigt, Donald E.; Fegyveresi, John M.; Stevens, Nathan T.; Spencer, Matthew K.; Cole-Dai, Jihong; Alley, Richard B.; Jardine, Gabriella E.; Cravens, Eric; Wilen, Lawrence A.; Fudge, T. J.; McConnell, Joseph R.

2014-01-01

The WAIS (West Antarctic Ice Sheet) Divide deep ice core was recently completed to a total depth of 3405 m, ending ∼50 m above the bed. Investigation of the visual stratigraphy and grain characteristics indicates that the ice column at the drilling location is undisturbed by any large-scale overturning or discontinuity. The climate record developed from this core is therefore likely to be continuous and robust. Measured grain-growth rates, recrystallization characteristics, and grain-size response at climate transitions fit within current understanding. Significant impurity control on grain size is indicated from correlation analysis between impurity loading and grain size. Bubble-number densities and bubble sizes and shapes are presented through the full extent of the bubbly ice. Where bubble elongation is observed, the direction of elongation is preferentially parallel to the trace of the basal (0001) plane. Preferred crystallographic orientation of grains is present in the shallowest samples measured, and increases with depth, progressing to a vertical-girdle pattern that tightens to a vertical single-maximum fabric. This single-maximum fabric switches into multiple maxima as the grain size increases rapidly in the deepest, warmest ice. A strong dependence of the fabric on the impurity-mediated grain size is apparent in the deepest samples.

Clouds in the atmospheres of extrasolar planets. IV. On the scattering greenhouse effect of CO2 ice particles: Numerical radiative transfer studies

NASA Astrophysics Data System (ADS)

Kitzmann, D.; Patzer, A. B. C.; Rauer, H.

2013-09-01

Context. Owing to their wavelength-dependent absorption and scattering properties, clouds have a strong impact on the climate of planetary atmospheres. The potential greenhouse effect of CO2 ice clouds in the atmospheres of terrestrial extrasolar planets is of particular interest because it might influence the position and thus the extension of the outer boundary of the classic habitable zone around main sequence stars. Such a greenhouse effect, however, is a complicated function of the CO2 ice particles' optical properties. Aims: We study the radiative effects of CO2 ice particles obtained by different numerical treatments to solve the radiative transfer equation. To determine the effectiveness of the scattering greenhouse effect caused by CO2 ice clouds, the radiative transfer calculations are performed over the relevant wide range of particle sizes and optical depths, employing different numerical methods. Methods: We used Mie theory to calculate the optical properties of particle polydispersion. The radiative transfer calculations were done with a high-order discrete ordinate method (DISORT). Two-stream radiative transfer methods were used for comparison with previous studies. Results: The comparison between the results of a high-order discrete ordinate method and simpler two-stream approaches reveals large deviations in terms of a potential scattering efficiency of the greenhouse effect. The two-stream methods overestimate the transmitted and reflected radiation, thereby yielding a higher scattering greenhouse effect. For the particular case of a cool M-type dwarf, the CO2 ice particles show no strong effective scattering greenhouse effect by using the high-order discrete ordinate method, whereas a positive net greenhouse effect was found for the two-stream radiative transfer schemes. As a result, previous studies of the effects of CO2 ice clouds using two-stream approximations overrated the atmospheric warming caused by the scattering greenhouse effect

Dating an 800,000 year Antarctic ice core record using the isotopic composition of trapped air

NASA Astrophysics Data System (ADS)

Dreyfus, Gabrielle Boissier

Here we measure the isotopic composition of air trapped in the European Project for Ice Coring in Antarctica Dome C (EDC) ice core, and use this geochemical information to improve the ice core agescale and our understanding of air enclosure processes. A first result is the detection of a flow anomaly in the bottom 500m of the EDC ice core using the delta18O of atmospheric oxygen (noted delta18Oatm). By tuning the measured delta18Oatm to the orbital precession signal, we correct the EDC agescale over 400-800 ka for flow-induced distortions in the duration of events. Uncertainty in delta 18Oatm phasing with respect to precession limits the accuracy of the tuned agescale to +/-6 ka. We use this improved agescale to date two 10Be peaks detected in the EDC ice core and associated with the Matuyama-Brunhes geomagnetic boundary. While the ice age of the "precursor" event agrees within uncertainty with the age of radioisotopically dated lavas, the volcanic age for the younger reversal is approximately 10 ka older than the mid-point of the 10 Be peak in the ice. Since 80% of the lavas recording the Matuyama-Brunhes reversal are located in the Central Pacific, the observed age difference may indicate that the magnetic field orientation at this location changed prior to the dipole intensity minimum recorded by the ice core 10Be, as suggested by recent geodynamo modeling. A particular challenge for ice core dating is accurately accounting for the age difference between the trapped air and surrounding ice. This gas age - ice age difference (noted Deltaage) depends on the age of the ice at the bottom of the firn. delta15N of N2 is constant in the atmosphere over the timescales considered here, so any deviation from atmospheric composition reflects fractionation processes in the firn. We show that delta15N is positively correlated with the ice deuterium content, a proxy for temperature, over the entire EDC record, and propose an accumulation-permeability-convection mechanism

Synthesis and properties MFe2O4 (M = Fe, Co) nanoparticles and core-shell structures

NASA Astrophysics Data System (ADS)

Yelenich, O. V.; Solopan, S. O.; Greneche, J. M.; Belous, A. G.

2015-08-01

Individual Fe3-xO4 and CoFe2O4 nanoparticles, as well as Fe3-xO4/CoFe2O4 core/shell structures were synthesized by the method of co-precipitation from diethylene glycol solutions. Core/shell structure were synthesized with CoFe2O4-shell thickness of 1.0, 2.5 and 3.5 nm. X-ray diffraction patterns of individual nanoparticles and core/shell are similar and indicate that all synthesized samples have a cubic spinel structure. Compares Mössbauer studies of CoFe2O4, Fe3-xO4 nanoparticles indicate superparamagnetic properties at 300 K. It was shown that individual magnetite nanoparticles are transformed into maghemite through oxidation during the synthesis procedure, wherein the smallest nanoparticles are completely oxidized while a magnetite core does occur in the case of the largest nanoparticles. The Mössbauer spectra of core/shell nanoparticles with increasing CoFe2O4-shell thickness show a gradual decrease in the relative intensity of the quadrupole doublet and significant decrease of the mean isomer shift value at both RT and 77 K indicating a decrease of the superparamagnetic relaxation phenomena. Specific loss power for the prepared ferrofluids was experimentally calculated and it was determined that under influence of ac-magnetic field magnetic fluid based on individual CoFe2O4 and Fe3-xO4 particles are characterized by very low heating temperature, when magnetic fluids based on core/shell nanoparticles demonstrate higher heating effect.

Implications for carbon processing beneath the Greenland Ice Sheet from dissolved CO2 and CH4 concentrations of subglacial discharge

NASA Astrophysics Data System (ADS)

Pain, A.; Martin, J.; Martin, E. E.

2017-12-01

Subglacial carbon processes are of increasing interest as warming induces ice melting and increases fluxes of glacial meltwater into proglacial rivers and the coastal ocean. Meltwater may serve as an atmospheric source or sink of carbon dioxide (CO2) or methane (CH4), depending on the magnitudes of subglacial organic carbon (OC) remineralization, which produces CO2 and CH4, and mineral weathering reactions, which consume CO2 but not CH4. We report wide variability in dissolved CO2 and CH4 concentrations at the beginning of the melt season (May-June 2017) between three sites draining land-terminating glaciers of the Greenland Ice Sheet. Two sites, located along the Watson River in western Greenland, drain the Isunnguata and Russell Glaciers and contained 1060 and 400 ppm CO2, respectively. In-situ CO2 flux measurements indicated that the Isunnguata was a source of atmospheric CO2, while the Russell was a sink. Both sites had elevated CH4 concentrations, at 325 and 25 ppm CH4, respectively, suggesting active anaerobic OC remineralization beneath the ice sheet. Dissolved CO2 and CH4 reached atmospheric equilibrium within 2.6 and 8.6 km downstream of Isunnguata and Russell discharge sites, respectively. These changes reflect rapid gas exchange with the atmosphere and/or CO2 consumption via instream mineral weathering. The third site, draining the Kiagtut Sermiat in southern Greenland, had about half atmospheric CO2 concentrations (250 ppm), but approximately atmospheric CH4 concentrations (2.1 ppm). Downstream CO2 flux measurements indicated ingassing of CO2 over the entire 10-km length of the proglacial river. CO2 undersaturation may be due to more readily weathered lithologies underlying the Kiagtut Sermiat compared to Watson River sites, but low CH4 concentrations also suggest limited contributions of CO2 and CH4 from OC remineralization. These results suggest that carbon processing beneath the Greenland Ice Sheet may be more variable than previously recognized

High-resolution Sulfur Isotopes in Ice Cores Identify Large Stratospheric Eruptions

NASA Astrophysics Data System (ADS)

Burke, A.; Sigl, M.; Moore, K.; Nita, D. C.; Adkins, J. F.; Paris, G.; McConnell, J.

2016-12-01

The record of the volcanic forcing of climate over the past 2500 years is reconstructed primarily from sulfate concentrations in ice cores. Of particular interest are stratospheric eruptions, as these afford sulfate aerosols the longest residence time and largest dispersion in the atmosphere, and thus the greatest impact on radiative forcing. Identification of stratospheric eruptions currently relies on the successful matching of the same volcanic sulfate peak in ice cores from both the Northern and Southern hemispheres (a "bipolar event"). These are interpreted to reflect the global distribution of sulfur aerosols by the stratospheric winds. Despite its recent success, this method relies on precise and accurate dating of ice cores, in order to distinguish between a true `bipolar event' and two separate eruptions that occurred in close temporal succession. Sulfur isotopes can been used to distinguish between these two scenarios since stratospheric sulfur aerosols are exposed to UV radiation which imparts a mass independent fractionation (Baroni et al., 2007). Mass independent fractionation of sulfate in ice cores thus offers a novel method of fingerprinting stratospheric eruptions, and thus refining the historic record of explosive volcanism and its forcing of climate. Here we present new high-resolution (sub-annual) sulfur isotope data from the Tunu Ice core in Greenland over seven eruptions. Sulfur isotopes were measured by MC-ICP-MS, which substantially reduces sample size requirements and allows high temporal resolution from a single ice core. We demonstrate the efficacy of the method on recent, well-known eruptions (including Pinatubo and Katmai/Novarupta), and then apply it to unidentified sulfate peaks, allowing us to identify new stratospheric eruptions. Baroni, M., Thiemens, M. H., Delmas, R. J., & Savarino, J. (2007). Mass-independent sulfur isotopic compositions in stratospheric volcanic eruptions. Science, 315(5808), 84-87. http://doi.org/10

A New Fast, Reliable Technique for the Sampling of Dissolved Inorganic Carbon in Sea Ice

NASA Astrophysics Data System (ADS)

Hu, Y.; Wang, F.; Rysgaard, S.; Barber, D. G.

2015-12-01

For a long time, sea ice was considered to act as a lid over seawater preventing CO2 exchange between the atmosphere and ocean. Recent observations suggest that sea ice can be an active source or a sink for CO2, although its magnitude is not very clear. The direct measurements on CO2 flux based on the chamber method and eddy covariance often do not agree with each other. It is therefore important to measure the dissolved inorganic carbon (DIC) stock in sea ice precisely in order to better understand the CO2 flux through sea ice. The challenges in sea ice DIC sampling is how to melt the ice core without being exposed to the air gaining or losing CO2. A common practice is to seal the ice core in a self-prepared gas-tight plastic bag and suck the air out of the bag gently using a syringe (together with a needle) through a valve mounted on one side of the bag. However, this method is time consuming (takes up to several minutes to suck the air out) and very often there is large headspace found in the bag after the ice melts due to the imperfect bag-preparation, which might affect the DIC concentration in melt ice-water. We developed a new technique by using a commercially available plastic bag with a vacuum sealer to seal the ice core. In comparison to syringe-based method, this technique is fast and easy to operate; it takes less than 10 seconds to vacuum and seal the bag all in one button with no headspace left in the bag. Experimental tests with replicate ice cores sealed by those two methods showed that there is no difference in the DIC concentration measured after these two methods, suggesting that there is no loss of DIC during the course of vacuum sealing. In addition, a time series experiment on DIC in melt ice-water stored in the new bag shows that when the samples were not poisoned, the DIC concentration remains unchanged for at least 3 days in the bag; while poisoned by HgCl2, there is no change in DIC for at least 21 days, indicating that this new bag is

Ice Chemistry on Outer Solar System Bodies: Electron Radiolysis of N2-, CH4-, and CO-Containing Ices

NASA Astrophysics Data System (ADS)

Materese, Christopher K.; Cruikshank, Dale P.; Sandford, Scott A.; Imanaka, Hiroshi; Nuevo, Michel

2015-10-01

Radiation processing of the surface ices of outer Solar System bodies may be an important process for the production of complex chemical species. The refractory materials resulting from radiation processing of known ices are thought to impart to them a red or brown color, as perceived in the visible spectral region. In this work, we analyzed the refractory materials produced from the 1.2-keV electron bombardment of low-temperature N2-, CH4-, and CO-containing ices (100:1:1), which simulates the radiation from the secondary electrons produced by cosmic ray bombardment of the surface ices of Pluto. Despite starting with extremely simple ices dominated by N2, electron irradiation processing results in the production of refractory material with complex oxygen- and nitrogen-bearing organic molecules. These refractory materials were studied at room temperature using multiple analytical techniques including Fourier-transform infrared spectroscopy, X-ray absorption near-edge structure (XANES) spectroscopy, and gas chromatography coupled with mass spectrometry (GC-MS). Infrared spectra of the refractory material suggest the presence of alcohols, carboxylic acids, ketones, aldehydes, amines, and nitriles. XANES spectra of the material indicate the presence of carboxyl groups, amides, urea, and nitriles, and are thus consistent with the IR data. Atomic abundance ratios for the bulk composition of these residues from XANES analysis show that the organic residues are extremely N-rich, having ratios of N/C ∼ 0.9 and O/C ∼ 0.2. Finally, GC-MS data reveal that the residues contain urea as well as numerous carboxylic acids, some of which are of interest for prebiotic and biological chemistries.

eVolv2k: A new ice core-based volcanic forcing reconstruction for the past 2000 years

NASA Astrophysics Data System (ADS)

Toohey, Matthew; Sigl, Michael

2016-04-01

Radiative forcing resulting from stratospheric aerosols produced by major volcanic eruptions is a dominant driver of climate variability in the Earth's past. The ability of climate model simulations to accurately recreate past climate is tied directly to the accuracy of the volcanic forcing timeseries used in the simulations. We present here a new volcanic forcing reconstruction, based on newly updated ice core composites from Antarctica and Greenland. Ice core records are translated into stratospheric aerosol properties for use in climate models through the Easy Volcanic Aerosol (EVA) module, which provides an analytic representation of volcanic stratospheric aerosol forcing based on available observations and aerosol model results, prescribing the aerosol's radiative properties and primary modes of spatial and temporal variability. The evolv2k volcanic forcing dataset covers the past 2000 years, and has been provided for use in the Paleo-Modeling Intercomparison Project (PMIP), and VolMIP experiments within CMIP6. Here, we describe the construction of the eVolv2k data set, compare with prior forcing sets, and show initial simulation results.

The tephrostratigraphy of Mt. Berlin volcano, Antarctica: Integrating blue ice tephra and ice core tephra records

NASA Astrophysics Data System (ADS)

Iverson, N. A.; Dunbar, N. W.; McIntosh, W. C.; Kurbatov, A.

2016-12-01

Reconstructing volcanic activity in Antarctica is difficult because of the limited outcrop exposure. However, ice is an excellent medium for sampling tephra, allowing for a more complete eruptive record than can be found in other depositional environments. Furthermore, because of low ambient temperature, glass shards trapped in ice remain unaltered and unhydrated. Mt. Berlin is an ice covered volcano in Marie Byrd Land, Antarctica, and, because of heavy glaciation, eruptive records on the volcano itself are sparse. Here, we present the integration of two different records of Mt. Berlin volcanism: the blue ice record found at Mt. Moulton (Dunbar et al., 2008) and the ice core record from the WAIS Divide ice core. Tephra from Mt. Berlin are also found in other ice and marine core records, and these have been correlated and integrated into the combined volcanic record. The Mt. Moulton blue ice area is located 30 km from Mt. Berlin and hosts a fabulous tephra record spanning the last 500 ka. A total of 36 tephra from Mt. Berlin were sampled in stratigraphic order and nine were directly dated by 40Ar/39Ar dating method. Twenty five tephra from WAIS Divide have been analyzed and are geochemically similar to Mt. Berlin with ice core ages dating back to 70 ka. The two tephra records were integrated using their respective timescales. In locations where the Mt. Moulton record does not have precise chronology, the δ18O records from Mt. Moulton (Popp, 2008) and WAIS (WAIS, 2015) were used to integrate the stratigraphy. In total 61 tephra from both ice sections provide an excellent record of the magmatic evolution of Mt. Berlin over the past 500 ka. EMP analyses on glass shards show a gradual change in Fe and S over time. Most of the other major elements remain relatively unchanged. The trend in Fe and S could be produced by progressive tapping of a single, stratified magma chamber, but the long duration of volcanism makes this unlikely. We instead favor small batches of

Younger Dryas cooling and the Greenland climate response to CO2.

PubMed

Liu, Zhengyu; Carlson, Anders E; He, Feng; Brady, Esther C; Otto-Bliesner, Bette L; Briegleb, Bruce P; Wehrenberg, Mark; Clark, Peter U; Wu, Shu; Cheng, Jun; Zhang, Jiaxu; Noone, David; Zhu, Jiang

2012-07-10

Greenland ice-core δ(18)O-temperature reconstructions suggest a dramatic cooling during the Younger Dryas (YD; 12.9-11.7 ka), with temperatures being as cold as the earlier Oldest Dryas (OD; 18.0-14.6 ka) despite an approximately 50 ppm rise in atmospheric CO(2). Such YD cooling implies a muted Greenland climate response to atmospheric CO(2), contrary to physical predictions of an enhanced high-latitude response to future increases in CO(2). Here we show that North Atlantic sea surface temperature reconstructions as well as transient climate model simulations suggest that the YD over Greenland should be substantially warmer than the OD by approximately 5 °C in response to increased atmospheric CO(2). Additional experiments with an isotope-enabled model suggest that the apparent YD temperature reconstruction derived from the ice-core δ(18)O record is likely an artifact of an altered temperature-δ(18)O relationship due to changing deglacial atmospheric circulation. Our results thus suggest that Greenland climate was warmer during the YD relative to the OD in response to rising atmospheric CO(2), consistent with sea surface temperature reconstructions and physical predictions, and has a sensitivity approximately twice that found in climate models for current climate due to an enhanced albedo feedback during the last deglaciation.

Towards a new common Greenland Ice Core Chronology for the last 5000 years

NASA Astrophysics Data System (ADS)

Winstrup, Mai; Olander Rasmussen, Sune; Møllesøe Vinther, Bo; Cook, Eliza; Svensson, Anders; McConnell, Joe; Steffensen, Jørgen Peder

2017-04-01

Since the development of the Greenland Ice Core Chronology 2005 (GICC05), it has been widely used as a reference chronology in paleoclimate research. However, recent research (Sigl et al, 2015) demonstrated that this timescale has small, but significant, issues over historical time. These discrepancies was found by counting annual layers in high-resolution chemistry records from the NEEM S1 shallow core, and confirmed by linking via 10Be marker horizons to the layer-counted WAIS Divide ice core, Antarctica, and accurately-dated tree-ring series. This work showed that a revision of GICC05 is required prior to 1250AD. We here refine and extend this work. Layer-counting in a single core will always involve some uncertainty, and we hence use data from multiple Greenland ice cores, for which high-resolution impurity records recently have been measured. These ice cores have been synchronized using volcanic marker horizons, and the layer-counting is performed automatically using the StratiCounter algorithm (Winstrup et al, 2012), while ensuring that the number of layers between volcanic horizons are the same in all cores. Based on this extended multiple-core data set, we are further able to extend the new Greenland timescale another few thousand years back in time. This will, among others, provide a new ice-core date for the catastrophic volcanic eruption ( 1600 BC) that destroyed the Greek Minoan culture, an important time marker in Greek history.

Permafrost carbon as a missing link to explain CO 2 changes during the last deglaciation

NASA Astrophysics Data System (ADS)

Crichton, K. A.; Bouttes, N.; Roche, D. M.; Chappellaz, J.; Krinner, G.

2016-09-01

The atmospheric concentration of CO2 increased from 190 to 280 ppm between the last glacial maximum 21,000 years ago and the pre-industrial era. This CO2 rise and its timing have been linked to changes in the Earth’s orbit, ice sheet configuration and volume, and ocean carbon storage. The ice-core record of δ13CO2 (refs ,) in the atmosphere can help to constrain the source of carbon, but previous modelling studies have failed to capture the evolution of δ13CO2 over this period. Here we show that simulations of the last deglaciation that include a permafrost carbon component can reproduce the ice core records between 21,000 and 10,000 years ago. We suggest that thawing permafrost, due to increasing summer insolation in the northern hemisphere, is the main source of CO2 rise between 17,500 and 15,000 years ago, a period sometimes referred to as the Mystery Interval. Together with a fresh water release into the North Atlantic, much of the CO2 variability associated with the Bølling-Allerod/Younger Dryas period ~15,000 to ~12,000 years ago can also be explained. In simulations of future warming we find that the permafrost carbon feedback increases global mean temperature by 10-40% relative to simulations without this feedback, with the magnitude of the increase dependent on the evolution of anthropogenic carbon emissions.

Paleoclimatic significance of insoluble microparticle records from Canadian Arctic and Greenland ice cores

NASA Astrophysics Data System (ADS)

Zdanowicz, Christian Michel

1999-10-01

The past and present variability of climate in the Arctic region is investigated using ice core records of atmospheric dust (microparticles) and volcanic aerosols developed from the Canadian Arctic and Greenland. A high- resolution, 10 4-year long proxy record of atmospheric dust deposition is developed from an ice core (P95) drilled through the Penny Ice Cap, Baffin Island. Snowpit studies indicate that dust deposited on the Penny Ice Cap are representative of background mineral aerosol, and demonstrate that the variability of dust fallout is preserved in the P95 core at multi-annual to longer time scales. The P95 dust record reveals a significant increase in dust deposition on the Penny Ice Cap between ca 7500-5000 yr ago. This increase was driven by early to mid-/late Holocene transformations in the Northern Hemisphere landscape (ice cover retreat, postglacial land emergence) and climate (transition to colder, drier conditions) that led to an expansion of sources and enhanced eolian activity. Comparison between dust records in the P95 and GISP2 (Greenland) ice cores shows an increasing divergence between the two records beginning ca 7500 years ago. The effects of Northern Hemisphere atmospheric circulation and snow cover extent on atmospheric dust deposition in the Arctic are evaluated by comparing the P95 dust record with observational data. Changes in dust deposition are strongly linked to modes of the Northern Hemisphere winter circulation. Most prominently, an inverse relationship between the P95 dust record and the intensity of the winter Siberian High accounts for over 50% of the interannual variance of these two parameters over the period 1899-1995. On inter- to multi- annual time scales, the P95 dust record is significantly anticorrelated with variations in spring, and to a lesser extent fall, snow cover extent in the mid-latitude interior regions of Eurasia and North America. These relationships account for an estimated 10 to 20% of variance in the P95

Hydrogenated CoOx nanowire@Ni(OH)2 nanosheet core-shell nanostructures for high-performance asymmetric supercapacitors

NASA Astrophysics Data System (ADS)

Zhu, Jianxiao; Huang, Lei; Xiao, Yuxiu; Shen, Leo; Chen, Qi; Shi, Wangzhou

2014-05-01

We report a facile strategy to prepare 3D core-shell nanowire heterostructures with microporous hydrogenated CoOx (H-CoOx) nanowires as the conducting scaffold to support Ni(OH)2 nanosheets. Benefiting from the H-CoOx nanowire core to provide the effective pathway for charge transport and the core-shell heterostructures with synergistic effects, the H-CoOx@Ni(OH)2 core-shell nanowire electrode achieved the specific capacitance of 2196 F g-1 (areal capacitance of 5.73 F cm-2), which is approximately a 1.4-fold enhancement compared with the Co3O4@Ni(OH)2 core-shell nanowires. An aqueous asymmetric supercapacitor (ASC) device was fabricated by using H-CoOx@Ni(OH)2 nanowires as the positive electrode and reduced graphene oxide @Fe3O4 nanocomposites as the negative electrode. The ASCs achieved high energy density (~45.3 W h kg-1 at 1010 W kg-1), high power density (~7080 W kg-1 at 23.4 W h kg-1) and high cycling stability. Furthermore, after charging for ~1 min, one such 22 cm2 ASC device demonstrated to be able to drive a small windmill (0.8 V, 0.1 W) for 20 min. Two such ASCs connected in series can power up a seven-color LED (3.2 V) efficiently.We report a facile strategy to prepare 3D core-shell nanowire heterostructures with microporous hydrogenated CoOx (H-CoOx) nanowires as the conducting scaffold to support Ni(OH)2 nanosheets. Benefiting from the H-CoOx nanowire core to provide the effective pathway for charge transport and the core-shell heterostructures with synergistic effects, the H-CoOx@Ni(OH)2 core-shell nanowire electrode achieved the specific capacitance of 2196 F g-1 (areal capacitance of 5.73 F cm-2), which is approximately a 1.4-fold enhancement compared with the Co3O4@Ni(OH)2 core-shell nanowires. An aqueous asymmetric supercapacitor (ASC) device was fabricated by using H-CoOx@Ni(OH)2 nanowires as the positive electrode and reduced graphene oxide @Fe3O4 nanocomposites as the negative electrode. The ASCs achieved high energy density (~45.3 W h kg-1 at

Estimating Last Glacial Maximum Ice Thickness Using Porosity and Depth Relationships: Examples from AND-1B and AND-2A Cores, McMurdo Sound, Antarctica

NASA Astrophysics Data System (ADS)

Hayden, T. G.; Kominz, M. A.; Magens, D.; Niessen, F.

2009-12-01

We have estimated ice thicknesses at the AND-1B core during the Last Glacial Maximum by adapting an existing technique to calculate overburden. As ice thickness at Last Glacial Maximum is unknown in existing ice sheet reconstructions, this analysis provides constraint on model predictions. We analyze the porosity as a function of depth and lithology from measurements taken on the AND-1B core, and compare these results to a global dataset of marine, normally compacted sediments compiled from various legs of ODP and IODP. Using this dataset we are able to estimate the amount of overburden required to compact the sediments to the porosity observed in AND-1B. This analysis is a function of lithology, depth and porosity, and generates estimates ranging from zero to 1,000 meters. These overburden estimates are based on individual lithologies, and are translated into ice thickness estimates by accounting for both sediment and ice densities. To do this we use a simple relationship of Xover * (ρsed/ρice) = Xice; where Xover is the overburden thickness, ρsed is sediment density (calculated from lithology and porosity), ρice is the density of glacial ice (taken as 0.85g/cm3), and Xice is the equalivant ice thickness. The final estimates vary considerably, however the “Best Estimate” behavior of the 2 lithologies most likely to compact consistently is remarkably similar. These lithologies are the clay and silt units (Facies 2a/2b) and the diatomite units (Facies 1a) of AND-1B. These lithologies both produce best estimates of approximately 1,000 meters of ice during Last Glacial Maximum. Additionally, while there is a large range of possible values, no combination of reasonable lithology, compaction, sediment density, or ice density values result in an estimate exceeding 1,900 meters of ice. This analysis only applies to ice thicknesses during Last Glacial Maximum, due to the overprinting effect of Last Glacial Maximum on previous ice advances. Analysis of the AND-2A

Rapid ice drilling with continual air transport of cuttings and cores: General concept

NASA Astrophysics Data System (ADS)

Wang, Rusheng; An, Liu; Cao, Pinlu; Chen, Baoyi; Sysoev, Mikhail; Fan, Dayou; Talalay, Pavel G.

2017-12-01

This article describes the investigation of the feasibility of rapid drilling in ice sheets and glaciers to depths of up to 600 m, with cuttings and cores continually transported by air reverse circulation. The method employs dual wall drill rods. The inner tubes provide a continuous pathway for the chips and cores from the drill bit face to the surface. To modify air reverse circulation drilling technology according to the conditions of a specific glacier, original cutter drill bits and air processing devices (air-cooled aftercoolers, air receivers, coalescing filters, desiccant dryers) should be used. The airflow velocity for conveying a 60-mm diameter and 200-mm long ice core should not be lower than 22.5 m/s, and the minimal airflow rate for continual chip and cores transport is 6.8 m3/min at 2.3-2.6 MPa. Drilling of a 600-m deep hole can be accomplished within 1.5 days in the case of 24 h drilling operations. However, to avoid sticking while drilling through ice, the drilling depth should to be limited to 540 m at a temperature of -20 °C and to 418 m at a temperature of -10 °C.

Synthesis of basalt fiber@Zn1-xMgxO core/shell nanostructures for selective photoreduction of CO2 to CO

NASA Astrophysics Data System (ADS)

Kwak, Byeong Sub; Kim, Kang Min; Park, Sun-Min; Kang, Misook

2017-06-01

This study focused on the development of a catalyst for converting carbon dioxide, the main cause of global warming, into a beneficial energy source. Core@shell structured particles, BF@ZnO and BF@Zn1-xMgxO, are synthesized in order to selectively obtain CO gas from the photoreduction of CO2. A modified sol-gel process is used to synthesize the core@shell structures with a three-dimensional microstructure, which are subsequently characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometry (EDAX), ultraviolet (UV)-vis absorption, photoluminescence (PL), and photocurrent density analysis. The CO2 adsorption abilities of the core@shell particles are estimated through CO2-temperature programmed desorption (TPD). The core@shell structured BF@Zn1-xMgxO particles including the Mg ingredient significantly increased the adsorption of CO2 gas at the microfiber/nanoparticle interface. Both the BF@ZnO and BF@Zn1-xMgxO particles selectively reduce the carbon dioxide to carbon monoxide, with almost no other reduced products being observed. These results are attributed to the effective adsorption of CO2 gas and inhibited recombination of the photogenerated electron-hole pairs. BF@Zn0.75Mg0.25O exhibited superior photocatalytic behavior and selectively produced 5.0 μmolgcat-1 L-1 of CO gas after 8 h of reaction.

The Mount Logan (Yukon) Ice Cores: Preliminary Results

NASA Astrophysics Data System (ADS)

Fisher, D. A.

2004-05-01

Three ice cores were taken at different elevations on or near My Logan in the years 2001 and 2002. The summit core (PRCol) comes from the summit plateau ( 5340 masl, length 187 m to bedrock, mean temperature -29 C ) and was done by the Geological Survey of Canada. The NIPR group cored 210m on the flanks of the mountain at King Col (4200 masl mean temperature -16C) and the UNH group cored 20 km from the mountain at Eclipse "Dome" (3015 masl,length 345 m mean temperature -5C) . The three cores were done cooperatively by GSC, NIPR and UNH and cover nominally 30 ka, 1 ka and 2ka respectively . Located very close to the Gulf of Alaska these core records are thought to reflect the climate history of the Pacific Ocean and having three widely spaced elevations, the sites "see" different distances to different sources. The lowest site (Eclipse) has excellent seasonals but a very muted δ 18O history with no obvious little ice age, whereas the most recent 1ka of the PRCol summit sites contains two very large and sudden δ 18O and d (deuterium excess) shifts at 1850 AD and ~ 800 AD. The δ 18O shifts which happen from one year to the next are about 4 o/oo . The summit site (PRCol) δ 18O response is "backwards", ie the Little Ice Age δ 18O values are 4 o/oo more positive than recent ones. The PRCol δ 18O and d suggest that the source water can either be ëlocalí (Gulf of Alaska) or very distant (tropics) . The Eclipse site seems only to get the local water . A massive dust storm originating in central Asia (Gobi) in April 2001 dumped a visible layer all over the St Elias Mountains and this layer was sampled, to provide a calibration "Asian dust event". The satellite and isotoic signatures both agreed that Gobi was the source. The PRCol record covers the Holocene and well back into the ice age. The transition is defined by a sudden ECM shift on the flanks of a more gradual O18 shift. Acknowledgements. Logan consortium consists of : Geological Survey of Canada : Jocelyne

Bipolar volcanic events in ice cores and the Toba eruption at 74 ka BP (Invited)

NASA Astrophysics Data System (ADS)

Svensson, A.

2013-12-01

Acidity spikes in Greenland and Antarctic ice cores are applied as tracers of past volcanic activity. Besides providing information on the timing and magnitude of past eruptions, the acidity spikes are also widely used for synchronization of ice cores. All of the deep Greenland ice cores are thus synchronized throughout the last glacial cycle based on volcanic markers. Volcanic matching of ice cores from the two Hemispheres is much more challenging but it is feasible in periods of favourable conditions. Over the last two millennia, where ice cores are precisely dated, some 50 bipolar volcanic events have thus been identified. In order for an eruption to express a bipolar fingerprint it generally needs to be a low latitude eruption with stratospheric injection. Sometimes tephra is associated with the ice-core acidity spikes, but most often there is no tephra present in the ice. As yet, an unknown eruption occurring in 1259 AD is the only event reported to have deposited tephra in both Greenland and Antarctica. During the last glacial period bipolar volcanic matching is very challenging and very little work has been done, but recent high-resolution ice core records have the potential to provide bipolar ice core matching for some periods. Recently, Greenland and Antarctic ice cores have been linked by acidity spikes in the time window of the most recent eruption (the YTT eruption) of the Indonesian Toba volcano that is situated close to equator in Sumatra. Ash from this Toba event is widespread over large areas in Asia and has been identified as far west as Africa, but no corresponding tephra has been found in polar ice cores despite several attempts. The age of the YTT eruption is well constrained by recent Ar-Ar dating to have occurred some 74 ka ago close to the Marine Isotope Stage 4/5 boundary and close to the onset of the cold Greenland Stadial 20 and the corresponding mild Antarctic Isotopic Maxima 19 and 20. Surprisingly, no single outstanding acidity spike

A new method for geochemical characterization of atmospheric mineral dust from polar ice cores: preliminary results from Talos Dome ice core (East Antarctica, Pacific-Ross Sea sector)

NASA Astrophysics Data System (ADS)

Baccolo, Giovanni; Delmonte, Barbara; Clemenza, Massimiliano; Previtali, Ezio; Maggi, Valter

2015-04-01

Assessing the elemental composition of atmospheric dust entrapped in polar ice cores is important for the identification of the potential dust sources and thus for the reconstruction of past atmospheric circulation, at local, regional and global scale. Accurate determination of major and trace elements in the insoluble fraction of dust extracted from ice cores is also useful to better understand some geochemical and biogeochemical mechanisms which are linked with the climate system. The extremely reduced concentration of dust in polar ice (typical Antarctic concentrations during interglacials are in the range of 10 ppb), the limited availability of such samples and the high risk of contamination make these analyses a challenge. A new method based on low background Instrumental Neutron Activation Analysis (INAA) was specifically developed for this kind of samples. The method allows the determination of the concentration of up to 35 elements in extremely reduced dust samples (20-30 μg). These elements span from major to trace and ultra-trace elements. Preliminary results from TALDICE (TALos Dome Ice CorE, East Antarctica, Pacific-Ross Sea Sector) ice core are presented along with results from potential source areas in Victoria Land. A set of 5 samples from Talos Dome, corresponding to the last termination, MIS3, MIS4 and MIS6 were prepared and analyzed by INAA.

Atomistic and infrared study of CO-water amorphous ice onto olivine dust grain

NASA Astrophysics Data System (ADS)

Escamilla-Roa, Elizabeth; Moreno, Fernando; López-Moreno, J. Juan; Sainz-Díaz, C. Ignacio

2017-01-01

This work is a study of CO and H2O molecules as adsorbates that interact on the surface of olivine dust grains. Olivine (forsterite) is present on the Earth, planetary dust, in the interstellar medium (ISM) and in particular in comets. The composition of amorphous ice is very important for the interpretation of processes that occur in the solar system and the ISM. Dust particles in ISM are composed of a heterogeneous mixture of amorphous or crystalline silicates (e.g. olivine) organic material, carbon, and other minor constituents. These dust grains are embedded in a matrix of ices, such as H2O, CO, CO2, NH3, and CH4. We consider that any amorphous ice will interact and grow faster on dust grain surfaces. In this work we explore the adsorption of CO-H2O amorphous ice onto several (100) forsterite surfaces (dipolar and non-dipolar), by using first principle calculations based on density functional theory (DFT). These models are applied to two possible situations: i) adsorption of CO molecules mixed into an amorphous ice matrix (gas mixture) and adsorbed directly onto the forsterite surface. This interaction has lower adsorption energy than polar molecules (H2O and NH3) adsorbed on this surface; ii) adsorption of CO when the surface has previously been covered by amorphous water ice (onion model). In this case the calculations show that adsorption energy is low, indicating that this interaction is weak and therefore the CO can be desorbed with a small increase of temperature. Vibration spectroscopy for the most stable complex was also studied and the frequencies were in good agreement with experimental frequency values.

Deriving micro- to macro-scale seismic velocities from ice-core c axis orientations

NASA Astrophysics Data System (ADS)

Kerch, Johanna; Diez, Anja; Weikusat, Ilka; Eisen, Olaf

2018-05-01

One of the great challenges in glaciology is the ability to estimate the bulk ice anisotropy in ice sheets and glaciers, which is needed to improve our understanding of ice-sheet dynamics. We investigate the effect of crystal anisotropy on seismic velocities in glacier ice and revisit the framework which is based on fabric eigenvalues to derive approximate seismic velocities by exploiting the assumed symmetry. In contrast to previous studies, we calculate the seismic velocities using the exact c axis angles describing the orientations of the crystal ensemble in an ice-core sample. We apply this approach to fabric data sets from an alpine and a polar ice core. Our results provide a quantitative evaluation of the earlier approximative eigenvalue framework. For near-vertical incidence our results differ by up to 135 m s-1 for P-wave and 200 m s-1 for S-wave velocity compared to the earlier framework (estimated 1 % difference in average P-wave velocity at the bedrock for the short alpine ice core). We quantify the influence of shear-wave splitting at the bedrock as 45 m s-1 for the alpine ice core and 59 m s-1 for the polar ice core. At non-vertical incidence we obtain differences of up to 185 m s-1 for P-wave and 280 m s-1 for S-wave velocities. Additionally, our findings highlight the variation in seismic velocity at non-vertical incidence as a function of the horizontal azimuth of the seismic plane, which can be significant for non-symmetric orientation distributions and results in a strong azimuth-dependent shear-wave splitting of max. 281 m s-1 at some depths. For a given incidence angle and depth we estimated changes in phase velocity of almost 200 m s-1 for P wave and more than 200 m s-1 for S wave and shear-wave splitting under a rotating seismic plane. We assess for the first time the change in seismic anisotropy that can be expected on a short spatial (vertical) scale in a glacier due to strong variability in crystal-orientation fabric (±50 m s-1 per 10 cm

McCall Glacier record of Arctic climate change: Interpreting a northern Alaska ice core with regional water isotopes

NASA Astrophysics Data System (ADS)

Klein, E. S.; Nolan, M.; McConnell, J.; Sigl, M.; Cherry, J.; Young, J.; Welker, J. M.

2016-01-01

We explored modern precipitation and ice core isotope ratios to better understand both modern and paleo climate in the Arctic. Paleoclimate reconstructions require an understanding of how modern synoptic climate influences proxies used in those reconstructions, such as water isotopes. Therefore we measured periodic precipitation samples at Toolik Lake Field Station (Toolik) in the northern foothills of the Brooks Range in the Alaskan Arctic to determine δ18O and δ2H. We applied this multi-decadal local precipitation δ18O/temperature regression to ∼65 years of McCall Glacier (also in the Brooks Range) ice core isotope measurements and found an increase in reconstructed temperatures over the late-20th and early-21st centuries. We also show that the McCall Glacier δ18O isotope record is negatively correlated with the winter bidecadal North Pacific Index (NPI) climate oscillation. McCall Glacier deuterium excess (d-excess, δ2H - 8*δ18O) values display a bidecadal periodicity coherent with the NPI and suggest shifts from more southwestern Bering Sea moisture sources with less sea ice (lower d-excess values) to more northern Arctic Ocean moisture sources with more sea ice (higher d-excess values). Northern ice covered Arctic Ocean McCall Glacier moisture sources are associated with weak Aleutian Low (AL) circulation patterns and the southern moisture sources with strong AL patterns. Ice core d-excess values significantly decrease over the record, coincident with warmer temperatures and a significant reduction in Alaska sea ice concentration, which suggests that ice free northern ocean waters are increasingly serving as terrestrial precipitation moisture sources; a concept recently proposed by modeling studies and also present in Greenland ice core d-excess values during previous transitions to warm periods. This study also shows the efficacy and importance of using ice cores from Arctic valley glaciers in paleoclimate reconstructions.

Tephra layers in the Siple Dome and Taylor Dome ice cores, Antarctica: Sources and correlations

NASA Astrophysics Data System (ADS)

Dunbar, Nelia W.; Zielinski, Gregory A.; Voisins, Daniel T.

2003-08-01

Volcanic ash, or tephra layers, are found in the Taylor Dome, Siple Dome A, and Siple Dome B ice cores. Significant shard concentrations are found at a number of depths in all three cores. Electron and ion microprobe analyses indicate that the geochemical composition of most layers is basaltic, basanitic, or trachytic, and the geochemical signatures of the layers suggest derivation from the Pleiades volcanic center, Mt. Melbourne volcano, or small mafic centers, probably in the Royal Society Range area. Presence of tephra layers suggests an episode of previously unrecognized Antarctic volcanic activity between 1776 and 1805 A.D., from at least two volcanic centers. A strong geochemical correlation (D = 3.49 and 3.97 with a value of 4 considered identical) is observed between tephra layers at depth of 79.2 m in the Taylor Dome ice core, and layers between 97.2 and 97.7 m depth in the Siple B core. This correlation, and the highly accurate depth-age scale of the Siple B core suggest that the age of this horizon in the Taylor Dome ice core presented by [1998a, 2000] should be revised downward, to the younger age of 675 ± 25 years before 1995. This revised chronology is consistent with vertical strain measurements presented by [2003].

Massive CO2 Ice Deposits Sequestered in the South Polar Layered Deposits of Mars

USGS Publications Warehouse

Phillips, Roger J.; Davis, Brian J.; Tanaka, Kenneth L.; Byrne, Shane; Mellon, Michael T.; Putzig, Nathaniel E.; Haberle, Robert M.; Kahre, Melinda A.; Campbell, Bruce A.; Carter, Lynn M.; Smith, Isaac B.; Holt, John W.; Smrekar, Suzanne E.; Nunes, Daniel C.; Plaut, Jeffrey J.; Egan, Anthony F.; Titus, Timothy N.; Seu, Roberto

2011-01-01

Shallow Radar soundings from the Mars Reconnaissance Orbiter reveal a buried deposit of carbon dioxide (CO2) ice within the south polar layered deposits of Mars with a volume of 9500 to 12,500 cubic kilometers, about 30 times that previously estimated for the south pole residual cap. The deposit occurs within a stratigraphic unit that is uniquely marked by collapse features and other evidence of interior CO2 volatile release. If released into the atmosphere at times of high obliquity, the CO2 reservoir would increase the atmospheric mass by up to 80%, leading to more frequent and intense dust storms and to more regions where liquid water could persist without boiling.

Distance-dependent radiation chemistry: Oxidation versus hydrogenation of CO in electron-irradiated H2O/CO/H2O ices

DOE Office of Scientific and Technical Information (OSTI.GOV)

Petrik, Nikolay G.; Monckton, Rhiannon J.; Koehler, Sven

Electron-stimulated oxidation of CO in layered H2O/CO/H2O ices was investigated with infrared reflection-absorption spectroscopy (IRAS) as function of the distance of the CO layer from the water/vacuum interface. The results show that while both oxidation and reduction reactions occur within the irradiated water films, there are distinct regions where either oxidation or reduction reactions are dominant. At depths less than ~ 15 ML, CO oxidation dominates over the sequential hydrogenation of CO to methanol (CH3OH), and CO2 is the major product of CO oxidation, consistent with previous observations. At its highest yield, CO2 accounts for ~45% of all the reactedmore » CO. Another oxidation product is identified as the formate anion (HCO2-). In contrast, for CO buried more than ~ 35 ML below the water/vacuum interface, the CO-to-methanol conversion efficiency is close to 100%. Production of CO2 and formate are not observed for the more deeply buried CO layers, where hydrogenation dominates. Experiments with CO dosed on pre-irradiated ASW samples suggest that OH radicals are primarily responsible for the oxidation reactions. Possible mechanisms of CO oxidation, involving primary and secondary processes of water radiolysis at low temperature, are discussed. The observed distance-dependent radiation chemistry results from the higher mobility of hydrogen atoms that are created by the interaction of the 100 eV electrons with the water films. These hydrogen atoms, which are primarily created at or near the water/vacuum interface, can desorb from or diffuse into the water films, while the less-mobile OH radicals remain in the near-surface zone resulting in preferential oxidation reactions there. The diffusing hydrogen atoms are responsible for the hydrogenation reactions that are dominant for the more deeply buried CO layers.« less

Changes in Black Carbon Deposition to Antarctica from Two Ice Core Records, A.D. 1850-2000

NASA Technical Reports Server (NTRS)

Bisiaux, Marion M.; Edward, Ross; McConnell, Joseph R.; Curran, Mark A. J.; VanOmmen, Tas D.; Smith, Andrew M.; Neumann, Thomas A.; Pasteris, Daniel R.; Penner, Joyce E.; Taylor, Kendrick

2012-01-01

Continuous flow analysis was based on a steady sample flow and in-line detection of BC and other chemical substances as described in McConnell et al. (2007). In the cold room, previously cut one meter ice core sticks of 3x3cm, are melted continuously on a heated melter head specifically designed to eliminate contamination from the atmosphere or by the external parts of the ice. The melted ice from the most inner part of the ice stick is continuously pumped by a peristaltic pump and carried to a clean lab by Teflon lines. The recorded signal is continuous, integrating a sample volume of about 0.05 mL, for which the temporal resolution depends on the speed of melting, ice density and snow accumulation rate at the ice core drilling site. For annual accumulation derived from the WAIS and Law Dome ice cores, we assumed 3.1 cm water equivalent uncertainty in each year's accumulation from short scale spatial variability (glaciological noise) which was determined from several measurements of annual accumulation in multiple parallel ice cores notably from the WAIS Divide ice core site (Banta et al., 2008) and from South Pole site (McConnell et al., 1997; McConnell et al., 2000). Refractory black carbon (rBC) concentrations were determined using the same method as in (Bisiaux et al., 2011) and adapted to continuous flow measurements as described by (McConnell et al., 2007). The technique uses a single particle intracavity laser induced incandescence photometer (SP2, Droplet Measurement Technologies, Boulder, Colorado) coupled to an ultrasonic nebulizer/desolvation (CETAC UT5000) Flow Injection Analysis (FIA). All analyses, sample preparation etc, were performed in a class 100 cleanroom using anti contamination "clean techniques". The samples were not acidified.

Polar Ice Sheets Drive Paleohydroclimate Affecting Terrestrial Plant Distribution and CO2 Exchange Potential during the Upper Carboniferous

NASA Astrophysics Data System (ADS)

White, J. D.; Poulsen, C. J.; Montanez, I. P.; McElwain, J.; Wilson, J. P.; Hren, M. T.

2016-12-01

Variation in atmospheric CO2 concentration and presence or absence of polar ice sheets simulated for 310 mya using the GENESIS model show changes in terrestrial temperature, precipitation, and potential evapotranspiration at mid and lower latitudes. Classifying the data into Holdridge life zones for simulations with 280, 560, and 1120 ppm CO2, in the presence of a southern Gondwanan ice sheet resulted in progressive increase of cool temperate, humid-to-subhumid and tropical subhumid zones. Without the ice sheet, subtropical subhumid to semiarid zones expanded. Simulation results show that approximately 50% of the land area was classified as polar or tundra followed by 35 to 42%, depending on the scenario, classified as sub-tropical semiarid-to-subhumid. Only 5-8% were classified as temperate humid-to-subhumid or tropical humid-to-perhumid. Also, the absence of ice sheets reduced the moister sub-climates, such as within the tropical climate zone. Because different plant assemblages dominated each climate zone, for example cordaitaleans in the subtropical and medullosans and lycophytes in the tropics, physiological differences in these plants may have resulted in unequal CO2 exchange feedbacks to the atmosphere during climate shifts. Previous physiological modeling based on plant foliar traits indicates that late Paleozoic plant species differed in CO2 uptake capacity with highest sensitivity to water availability during periods with low atmospheric CO2 concentration. This implies that vegetation climate feedbacks during this period may have been non-uniform during climate change events. Inference of plant contribution to climate forcing must rely on understanding geographic distribution of affected vegetation, inherent vegetation physiological properties, and antecedent atmospheric CO2 concentrations. Our results indicate that seasonally dry climates prevailed in the low-latitude land area, and that slightly cooler temperatures than today must be considered. This

10Be evidence for the Matuyama-Brunhes geomagnetic reversal in the EPICA Dome C ice core.

PubMed

Raisbeck, G M; Yiou, F; Cattani, O; Jouzel, J

2006-11-02

An ice core drilled at Dome C, Antarctica, is the oldest ice core so far retrieved. On the basis of ice flow modelling and a comparison between the deuterium signal in the ice with climate records from marine sediment cores, the ice at a depth of 3,190 m in the Dome C core is believed to have been deposited around 800,000 years ago, offering a rare opportunity to study climatic and environmental conditions over this time period. However, an independent determination of this age is important because the deuterium profile below a depth of 3,190 m depth does not show the expected correlation with the marine record. Here we present evidence for enhanced 10Be deposition in the ice at 3,160-3,170 m, which we interpret as a result of the low dipole field strength during the Matuyama-Brunhes geomagnetic reversal, which occurred about 780,000 years ago. If correct, this provides a crucial tie point between ice cores, marine cores and a radiometric timescale.

The role of interfacial metal silicates on the magnetism in FeCo/SiO 2 and Fe 49% Co 49% V 2% /SiO 2 core/shell nanoparticles

DOE Office of Scientific and Technical Information (OSTI.GOV)

Desautels, R. D.; Freeland, J. W.; Rowe, M. P.

2015-05-07

We have investigated the role of spontaneously formed interfacial metal silicates on the magnetism of FeCo/SiO2 and Fe49%Co49%V2%/SiO2 core/shell nanoparticles. Element specific x-ray absorption and photoelectron spectroscopy experiments have identified the characteristic spectral features of metallic iron and cobalt from within the nanoparticle core. In addition, metal silicates of iron, cobalt, and vanadium were found to have formed spontaneously at the interface between the nanoparticle core and silica shell. X-ray magnetic circular dichroism experiments indicated that the elemental magnetism was a result of metallic iron and cobalt with small components from the iron, cobalt, and vanadium silicates. Magnetometry experiments havemore » shown that there was no exchange bias loop shift in the FeCo nanoparticles; however, exchange bias from antiferromagnetic vanadium oxide was measured in the V-doped nanoparticles. These results showed clearly that the interfacial metal silicates played a significant role in the magnetism of these core/shell nanoparticles, and that the vanadium percolated from the FeCo-cores into the SiO2-based interfacial shell.« less

High-resolution sulfur isotopes in ice cores identify large stratospheric volcanic eruptions

NASA Astrophysics Data System (ADS)

Burke, Andrea; Sigl, Michael; Adkins, Jess; Paris, Guillaume; McConnell, Joe

2016-04-01

The record of the volcanic forcing of climate over the past 2500 years is reconstructed primarily from sulfate concentrations in ice cores. Of particular interest are stratospheric eruptions, as these afford sulfate aerosols the longest residence time and largest dispersion in the atmosphere, and thus the greatest impact on radiative forcing. Identification of stratospheric eruptions currently relies on the successful matching of the same volcanic sulphate peak in ice cores from both the Northern and Southern hemispheres (a "bipolar event"). These are interpreted to reflect the global distribution of sulfur aerosols by the stratospheric winds. Despite its recent success, this method relies on precise and accurate dating of ice cores, in order to distinguish between a true 'bipolar event' and two separate eruptions that occurred in close temporal succession. Sulfur isotopes can been used to distinguish between these two scenarios since stratospheric sulfur aerosols are exposed to UV radiation which imparts a mass independent fractionation (Baroni et al., 2007). Mass independent fractionation of sulfate in ice cores thus offers a novel method of fingerprinting stratospheric eruptions, and thus refining the historic record of explosive volcanism and its forcing of climate. Here we present new high-resolution (sub-annual) sulfur isotope data from the Tunu Ice core in Greenland over seven eruptions. Sulfur isotopes were measured by MC-ICP-MS, which substantially reduces sample size requirements and allows high temporal resolution from a single ice core. We demonstrate the efficacy of the method on recent, well-known eruptions (including Pinatubo and Katmai/Novarupta), and then apply it to unidentified sulfate peaks, allowing us to identify new stratospheric eruptions. Baroni, M., Thiemens, M. H., Delmas, R. J., & Savarino, J. (2007). Mass-independent sulfur isotopic compositions in stratospheric volcanic eruptions. Science, 315(5808), 84-87. http://doi.org/10

CO2 Exsolution from CO2 Saturated Water: Core-Scale Experiments and Focus on Impacts of Pressure Variations.

PubMed

Xu, Ruina; Li, Rong; Ma, Jin; Jiang, Peixue

2015-12-15

For CO2 sequestration and utilization in the shallow reservoirs, reservoir pressure changes are due to the injection rate changing, a leakage event, and brine withdrawal for reservoir pressure balance. The amounts of exsolved CO2 which are influenced by the pressure reduction and the subsequent secondary imbibition process have a significant effect on the stability and capacity of CO2 sequestration and utilization. In this study, exsolution behavior of the CO2 has been studied experimentally using a core flooding system in combination with NMR/MRI equipment. Three series of pressure variation profiles, including depletion followed by imbibitions without or with repressurization and repetitive depletion and repressurization/imbibition cycles, were designed to investigate the exsolution responses for these complex pressure variation profiles. We found that the exsolved CO2 phase preferentially occupies the larger pores and exhibits a uniform spatial distribution. The mobility of CO2 is low during the imbibition process, and the residual trapping ratio is extraordinarily high. During the cyclic pressure variation process, the first cycle has the largest contribution to the amount of exsolved CO2. The low CO2 mobility implies a certain degree of self-sealing during a possible reservoir depletion.

Detailed history of atmospheric trace elements from the Quelccaya ice core (Southern Peru) during the last 1200 years

NASA Astrophysics Data System (ADS)

Uglietti, C.; Gabrielli, P.; Thompson, L. G.

2013-12-01

The recent increase in trace element concentrations, for example Cr, Cu, Zn, Ag, Pb, Bi, and U, in polar snow and ice has provided compelling evidence of a hemispheric change in atmospheric composition since the nineteenth century. This change has been concomitant with the expansion of the Industrial Revolution and points towards an anthropogenic source of trace elements in the atmosphere. There are very few low latitude trace element ice core records and these are believed to be sensitive to perturbations of regional significance. To date, these records have not been used to document a preindustrial anthropogenic impact on atmospheric composition at low latitudes. Ice cores retrieved from the tropical Andes are particularly interesting because they have the potential to reveal detailed information about the evolution and environmental consequences of mineral exploitation related to the Pre Inca Civilizations, the Inca Empire (1438-1533 AD) and the subsequent Spanish invasion and dominance (1532-1833 AD). The chemical record preserved in the ice of the Quelccaya ice cap (southern Peruvian Andes) offers the exceptional opportunity to geochemically constrain the composition of the tropical atmosphere at high resolution over the last ~1200 years. Quantification of twenty trace elements (Ag, Al, As, Bi, Cd, Co, Cr, Cu, Fe, Mn, Mo, Pb, Rb, Sb, Sn, Ti, Tl, U, V, and Zn) was performed by ICP-SFMS over 105 m of the Quelccaya North Dome core (5600 m asl, 128.57 m) by analyzing 2450 samples. This provides the first atmospheric trace element record in South America spanning continuously and at high resolution for the time period between 1990 and 790 AD. Ag, As, Bi, Cd, Cr, Co, Cu, Mn, Mo, Sb, Sn, Pb and Zn show increases in concentration and crustal enrichment factor starting at different times between 1450 and 1550 AD, in concomitance with the expansions of the Inca Empire and, subsequently, the Spanish Empire well before the inception of the Industrial Revolution. This

A 21 000-year record of fluorescent organic matter markers in the WAIS Divide ice core

NASA Astrophysics Data System (ADS)

D'Andrilli, Juliana; Foreman, Christine M.; Sigl, Michael; Priscu, John C.; McConnell, Joseph R.

2017-05-01

Englacial ice contains a significant reservoir of organic material (OM), preserving a chronological record of materials from Earth's past. Here, we investigate if OM composition surveys in ice core research can provide paleoecological information on the dynamic nature of our Earth through time. Temporal trends in OM composition from the early Holocene extending back to the Last Glacial Maximum (LGM) of the West Antarctic Ice Sheet Divide (WD) ice core were measured by fluorescence spectroscopy. Multivariate parallel factor (PARAFAC) analysis is widely used to isolate the chemical components that best describe the observed variation across three-dimensional fluorescence spectroscopy (excitation-emission matrices; EEMs) assays. Fluorescent OM markers identified by PARAFAC modeling of the EEMs from the LGM (27.0-18.0 kyr BP; before present 1950) through the last deglaciation (LD; 18.0-11.5 kyr BP), to the mid-Holocene (11.5-6.0 kyr BP) provided evidence of different types of fluorescent OM composition and origin in the WD ice core over 21.0 kyr. Low excitation-emission wavelength fluorescent PARAFAC component one (C1), associated with chemical species similar to simple lignin phenols was the greatest contributor throughout the ice core, suggesting a strong signature of terrestrial OM in all climate periods. The component two (C2) OM marker, encompassed distinct variability in the ice core describing chemical species similar to tannin- and phenylalanine-like material. Component three (C3), associated with humic-like terrestrial material further resistant to biodegradation, was only characteristic of the Holocene, suggesting that more complex organic polymers such as lignins or tannins may be an ecological marker of warmer climates. We suggest that fluorescent OM markers observed during the LGM were the result of greater continental dust loading of lignin precursor (monolignol) material in a drier climate, with lower marine influences when sea ice extent was higher and

Brief Communication: Ikaite (CaCO3·6H2O) discovered in Arctic sea ice

NASA Astrophysics Data System (ADS)

Dieckmann, G. S.; Nehrke, G.; Uhlig, C.; Göttlicher, J.; Gerland, S.; Granskog, M. A.; Thomas, D. N.

2010-05-01

We report for the first time on the discovery of calcium carbonate crystals as ikaite (CaCO3·6H2O) in sea ice from the Arctic (Kongsfjorden, Svalbard) as confirmed by morphology and indirectly by X-ray diffraction as well as XANES spectroscopy of its amorophous decomposition product. This finding demonstrates that the precipitation of calcium carbonate during the freezing of sea ice is not restricted to the Antarctic, where it was observed for the first time in 2008. This observation is an important step in the quest to quantify its impact on the sea ice driven carbon cycle.

Hydrogenated CoOx nanowire@Ni(OH)2 nanosheet core-shell nanostructures for high-performance asymmetric supercapacitors.

PubMed

Zhu, Jianxiao; Huang, Lei; Xiao, Yuxiu; Shen, Leo; Chen, Qi; Shi, Wangzhou

2014-06-21

We report a facile strategy to prepare 3D core-shell nanowire heterostructures with microporous hydrogenated CoOx (H-CoOx) nanowires as the conducting scaffold to support Ni(OH)2 nanosheets. Benefiting from the H-CoOx nanowire core to provide the effective pathway for charge transport and the core-shell heterostructures with synergistic effects, the H-CoOx@Ni(OH)2 core-shell nanowire electrode achieved the specific capacitance of 2196 F g(-1) (areal capacitance of 5.73 F cm(-2)), which is approximately a 1.4-fold enhancement compared with the Co3O4@Ni(OH)2 core-shell nanowires. An aqueous asymmetric supercapacitor (ASC) device was fabricated by using H-CoOx@Ni(OH)2 nanowires as the positive electrode and reduced graphene oxide @Fe3O4 nanocomposites as the negative electrode. The ASCs achieved high energy density (∼ 45.3 W h kg(-1) at 1010 W kg(-1)), high power density (∼ 7080 W kg(-1) at 23.4 W h kg(-1)) and high cycling stability. Furthermore, after charging for ∼ 1 min, one such 22 cm(2) ASC device demonstrated to be able to drive a small windmill (0.8 V, 0.1 W) for 20 min. Two such ASCs connected in series can power up a seven-color LED (3.2 V) efficiently.

A TEM analysis of nanoparticulates in a Polar ice core

DOE Office of Scientific and Technical Information (OSTI.GOV)

Esquivel, E.V.; Murr, L.E

2004-03-15

This paper explores the prospect for analyzing nanoparticulates in age-dated ice cores representing times in antiquity to establish a historical reference for atmospheric particulate regimes. Analytical transmission electron microscope (TEM) techniques were utilized to observe representative ice-melt water drops dried down on carbon/formvar or similar coated grids. A 10,000-year-old Greenland ice core was melted, and representative water drops were transferred to coated grids in a clean room environment. Essentially, all particulates observed were aggregates and either crystalline or complex mixtures of nanocrystals. Especially notable was the observation of carbon nanotubes and related fullerene-like nanocrystal forms. These observations are similar withmore » some aspects of contemporary airborne particulates including carbon nanotubes and complex nanocrystal aggregates.« less

Ice core records of climate variability on the Third Pole with emphasis on the Guliya ice cap, western Kunlun Mountains

NASA Astrophysics Data System (ADS)

Thompson, Lonnie G.; Yao, Tandong; Davis, Mary E.; Mosley-Thompson, Ellen; Wu, Guangjian; Porter, Stacy E.; Xu, Baiqing; Lin, Ping-Nan; Wang, Ninglian; Beaudon, Emilie; Duan, Keqin; Sierra-Hernández, M. Roxana; Kenny, Donald V.

2018-05-01

Records of recent climate from ice cores drilled in 2015 on the Guliya ice cap in the western Kunlun Mountains of the Tibetan Plateau, which with the Himalaya comprises the Third Pole (TP), demonstrate that this region has become warmer and moister since at least the middle of the 19th century. Decadal-scale linkages are suggested between ice core temperature and snowfall proxies, North Atlantic oceanic and atmospheric processes, Arctic temperatures, and Indian summer monsoon intensity. Correlations between annual-scale oxygen isotopic ratios (δ18O) and tropical western Pacific and Indian Ocean sea surface temperatures are also demonstrated. Comparisons of climate records during the last millennium from ice cores acquired throughout the TP illustrate centennial-scale differences between monsoon and westerlies dominated regions. Among these records, Guliya shows the highest rate of warming since the end of the Little Ice Age, but δ18O data over the last millennium from TP ice cores support findings that elevation-dependent warming is most pronounced in the Himalaya. This, along with the decreasing precipitation rates in the Himalaya region, is having detrimental effects on the cryosphere. Although satellite monitoring of glaciers on the TP indicates changes in surface area, only a few have been directly monitored for mass balance and ablation from the surface. This type of ground-based study is essential to obtain a better understanding of the rate of ice shrinkage on the TP.

The effect of acidified sample storage time on the determination of trace element concentration in ice cores by ICP-SFMS

NASA Astrophysics Data System (ADS)

Uglietti, C.; Gabrielli, P.; Lutton, A.; Olesik, J.; Thompson, L. G.

2012-12-01

Trace elements in micro-particles entrapped in ice cores are a valuable proxy of past climate and environmental variations. Inductively coupled plasma sector field mass spectrometry (ICP-SFMS) is generally recognized as a sensitive and accurate technique for the quantification of ultra-trace element concentrations in ice cores. Usually, ICP-SFMS analyses of ice core samples are performed by melting and acidifying aliquots. Acidification is important to transfer trace elements from particles into solution by partial and/or complete dissolution. Only elements in solution and in sufficiently small particles will be vaporized and converted to elemental ions in the plasma for detection by ICP-SFMS. However, experimental results indicate that differences in acidified sample storage time at room temperature may lead to the recovery of different trace element fractions. Moreover, different lithologies of the relatively abundant crustal material entrapped in the ice matrix could also influence the fraction of trace elements that are converted into elemental ions in the plasma. These factors might affect the determination of trace elements concentrations in ice core samples and hamper the comparison of results obtained from ice cores from different locations and/or epochs. In order to monitor the transfer of elements from particles into solution in acidified melted ice core samples during storage, a test was performed on sections from nine ice cores retrieved from low latitude drilling sites around the world. When compared to ice cores from polar regions, these samples are characterized by a relative high content of micro-particles that may leach trace elements into solution differently. Of the nine ice cores, five are from the Tibetan Plateau (Dasuopu, Guliya, Naimonanyi, Puruogangri and Dunde), two from the Andes (Quelccaya and Huascaran), one from Africa (Kilimanjaro) and one from the Eastern Alps (Ortles). These samples were decontaminated by triple rinsing, melted and

Polar ice magnetization: Comparison of results from NorthGRIP (Greenland) and Vostok (Antarctica) ice cores

NASA Astrophysics Data System (ADS)

Lanci, L.; Kent, D. V.

2007-12-01

Low temperature measurements of isothermal remanent magnetization (IRM) in Greenland ice spanning the last glacial and Holocene have shown that ice samples contain a measurable concentration of magnetic minerals which are part of the atmospheric aerosol. Assuming that the source materials do not change much with time, the concentration of magnetic minerals should be proportional to the measured concentration of dust in ice. We have indeed found a consistent linear relationship with the contents of dust. However, the linear relationship between low temperature ice magnetization vs. dust concentration has an offset, which when extrapolated to zero dust concentration would seemingly indicate that a significantly large magnetization corresponds to a null amount of dust in ice. Thermal relaxation experiments have shown that magnetic grains of nanometric size carry virtually all the uncorrelated magnetization. Magnetic measurements in Antarctic ice cores confirm the existence of a similar nanometric-size magnetic fraction, which also appear uncorrelated with measured aerosol concentration. The magnitude of the uncorrelated magnetization from Vostok is similar to that measured in NorthGRIP ice. Measurements of IRM at 250K suggest that the SP magnetic particles are in the size range of about 7-17 nm, which is compatible with the expected size of particles produced by ablation and subsequent condensation of meteorites in the atmosphere. The concentration of extraterrestrial material in NorthGRIP ice was estimated from the magnetic relaxation data based on a crude estimate of chondritic Ms. The resulting concentration of 0.78±0.22 ppb for Greenland is in good agreement with the outcome based on published iridium concentrations; a virtually identical concentration of 0.53±0.18 ppb has been measured in Vostok ice core.

Hydro-geophysical responses to the injection of CO2 in core plugs of Berea sandstone

NASA Astrophysics Data System (ADS)

Song, I.; Park, K. G.

2017-12-01

We have built a laboratory-scale core flooding system to measure the relative permeability of a core sample and the acoustic response to the CO2 saturation degree at in situ condition of pressure and temperature down to a few kilometer depths. The system consisted of an acoustic velocity core holder (AVC model from the Core Laboratories) between upstream where CO2 and H2O were injected separately and downstream where the mixed fluids came out of a core sample. Core samples with 4 cm in diameter and 5 cm in length of Berea sandstone were in turn placed in the core holder for confining and axial pressures. The flooding operations of the multiphase fluids were conducted through the sample at 40ºC in temperature and 8 MPa in backpressure. CO2 and H2O in the physical condition were injected separately into a sample at constant rate with various ratios. The two phases were mixed during flowing through the sample. The mixed fluids out of the sample were separated again by their different densities in a chamber equipped with a level gauge of the interface. From the level change of the water in the separator, we measured the volume of water coming out of the sample for each test with a constant ratio of the injection rates. Then it was possible to calculate the saturation degree of CO2 from the difference between input volume and output volume of water. The differential pressure between upstream and downstream was directly measured to calculate the relative permeability as a function of the CO2 saturation degree. We also conducted ultrasonic measurements using piezoelectric sensors on the end plugs. An electric pulse was given to a sensor on one end of sample, and then ultrasonic waves were recorded from the other end. The various ratios of injection rate of CO2 and H2O into Berea sandstone yielded a range of 0.1-0.7 in CO2 saturation degree. The relative permeability was obtained at the condition of steady-state flow for given stages from the velocity of each phase and

Ancient Biomolecules from Deep Ice Cores Reveal a Forested Southern Greenland

PubMed Central

Willerslev, Eske; Cappellini, Enrico; Boomsma, Wouter; Nielsen, Rasmus; Hebsgaard, Martin B.; Brand, Tina B.; Hofreiter, Michael; Bunce, Michael; Poinar, Hendrik N.; Dahl-Jensen, Dorthe; Johnsen, Sigfus; Steffensen, Jørgen Peder; Bennike, Ole; Schwenninger, Jean-Luc; Nathan, Roger; Armitage, Simon; de Hoog, Cees-Jan; Alfimov, Vasily; Christl, Marcus; Beer, Juerg; Muscheler, Raimund; Barker, Joel; Sharp, Martin; Penkman, Kirsty E.H.; Haile, James; Taberlet, Pierre; Gilbert, M. Thomas P.; Casoli, Antonella; Campani, Elisa; Collins, Matthew J.

2009-01-01

One of the major difficulties in paleontology is the acquisition of fossil data from the 10% of Earth’s terrestrial surface that is covered by thick glaciers and ice sheets. Here we reveal that DNA and amino acids from buried organisms can be recovered from the basal sections of deep ice cores and allow reconstructions of past flora and fauna. We show that high altitude southern Greenland, currently lying below more than two kilometers of ice, was once inhabited by a diverse array of conifer trees and insects that may date back more than 450 thousand years. The results provide the first direct evidence in support of a forested southern Greenland and suggest that many deep ice cores may contain genetic records of paleoenvironments in their basal sections. PMID:17615355

Synthesis of Co 2SnO 4@C core-shell nanostructures with reversible lithium storage

NASA Astrophysics Data System (ADS)

Qi, Yue; Du, Ning; Zhang, Hui; Wu, Ping; Yang, Deren

This paper reports the synthesis of Co 2SnO 4@C core-shell nanostructures through a simple glucose hydrothermal and subsequent carbonization approach. The as-synthesized Co 2SnO 4@C core-shell nanostructures have been applied as anode materials for lithium-ion batteries, which exhibit improved cyclic performance compared to pure Co 2SnO 4 nanocrystals. The carbon matrix has good volume buffering effect and high electronic conductivity, which may be responsible for the improved cyclic performance.

Identifying deformation mechanisms in the NEEM ice core using EBSD measurements

NASA Astrophysics Data System (ADS)

Kuiper, Ernst-Jan; Weikusat, Ilka; Drury, Martyn R.; Pennock, Gill M.; de Winter, Matthijs D. A.

2015-04-01

Deformation of ice in continental sized ice sheets determines the flow behavior of ice towards the sea. Basal dislocation glide is assumed to be the dominant deformation mechanism in the creep deformation of natural ice, but non-basal glide is active as well. Knowledge of what types of deformation mechanisms are active in polar ice is critical in predicting the response of ice sheets in future warmer climates and its contribution to sea level rise, because the activity of deformation mechanisms depends critically on deformation conditions (such as temperature) as well as on the material properties (such as grain size). One of the methods to study the deformation mechanisms in natural materials is Electron Backscattered Diffraction (EBSD). We obtained ca. 50 EBSD maps of five different depths from a Greenlandic ice core (NEEM). The step size varied between 8 and 25 micron depending on the size of the deformation features. The size of the maps varied from 2000 to 10000 grid point. Indexing rates were up to 95%, partially by saving and reanalyzing the EBSP patterns. With this method we can characterize subgrain boundaries and determine the lattice rotation configurations of each individual subgrain. Combining these observations with arrangement/geometry of subgrain boundaries the dislocation types can be determined, which form these boundaries. Three main types of subgrain boundaries have been recognized in Antarctic (EDML) ice core¹². Here, we present the first results obtained from EBSD measurements performed on the NEEM ice core samples from the last glacial period, focusing on the relevance of dislocation activity of the possible slip systems. Preliminary results show that all three subgrain types, recognized in the EDML core, occur in the NEEM samples. In addition to the classical boundaries made up of basal dislocations, subgrain boundaries made of non-basal dislocations are also common. ¹Weikusat, I.; de Winter, D. A. M.; Pennock, G. M.; Hayles, M

Initial results from geophysical surveys and shallow coring of the Northeast Greenland Ice Stream (NEGIS)

NASA Astrophysics Data System (ADS)

Vallelonga, P.; Christianson, K.; Alley, R. B.; Anandakrishnan, S.; Christian, J. E. M.; Dahl-Jensen, D.; Gkinis, V.; Holme, C.; Jacobel, R. W.; Karlsson, N. B.; Keisling, B. A.; Kipfstuhl, S.; Kjær, H. A.; Kristensen, M. E. L.; Muto, A.; Peters, L. E.; Popp, T.; Riverman, K. L.; Svensson, A. M.; Tibuleac, C.; Vinther, B. M.; Weng, Y.; Winstrup, M.

2014-07-01

The Northeast Greenland Ice Stream (NEGIS) is the sole interior Greenlandic ice stream. Fast flow initiates near the summit dome, and the ice stream terminates approximately 1000 km downstream in three large outlet glaciers that calve into the Greenland Sea. To better understand this important system, in the summer of 2012 we drilled a 67 m firn core and conducted ground-based radio-echo sounding (RES) and active-source seismic surveys at a site approximately 150 km downstream from the onset of streaming flow (NEGIS firn core, 75°37.61' N, 35°56.49' W). The site is representative of the upper part of the ice stream, while also being in a crevasse-free area for safe surface operations. Annual cycles were observed for insoluble dust, sodium and ammonium concentrations and for electrolytic conductivity, allowing a seasonally resolved chronology covering the past 400 yr. Annual layer thicknesses averaged 0.11 m ice equivalent (i.e.) for the period 1607-2011, although accumulation varied between 0.08 and 0.14 m i.e., likely due to flow-related changes in surface topography. Tracing of RES layers from the NGRIP (North Greenland Ice Core Project) ice core site shows that the ice at NEGIS preserves a climatic record of at least the past 51 kyr. We demonstrate that deep ice core drilling in this location can provide a reliable Holocene and late-glacial climate record, as well as helping to constrain the past dynamics and ice-lithosphere interactions of the Greenland Ice Sheet.

Monodisperse Metal-Organic Framework Nanospheres with Encapsulated Core-Shell Nanoparticles Pt/Au@Pd@{Co2(oba)4(3-bpdh)2}4H2O for the Highly Selective Conversion of CO2 to CO.

PubMed

Zhao, Xi; Xu, Haitao; Wang, XiaoXiao; Zheng, Zhizhong; Xu, Zhenliang; Ge, Jianping

2018-05-02

A new microporous metal-organic framework (MOF) with formula {Co 2 (oba) 4 (3-bpdh) 2 }4H 2 O [oba = 4,4'-oxybis(benzoic acid); 3-bpdh = N, N'-bis-(1-pyridine-3-yl-ethylidene)-hydrazine] was assembled, and its morphology was found to undergo a microrod-to-nanosphere transformation with temperature variation. Core-shell Au@Pd functional nanoparticles (NPs) were successfully encapsulated in the center of the monodisperse nanospheres, and Pt NPs were well-dispersed and fully immobilized on the surface of Au@Pd@1Co to build the Pt/Au@Pd@1Co composites, which exhibited NPs catalytic activity for the reverse water gas shift reaction. The core-shell Au@Pd NPs in MOF significantly enchanced the CO selectivity of the catalyst, and the Pt NP loading on the surface of the nanosphere afforded a desirable CO 2 conversion.

Chlorine-36 and cesium-137 in ice-core samples from mid-latitude glacial sites in the Northern Hemisphere

USGS Publications Warehouse

Green, J.R.; Cecil, L.D.; Synal, H.-A.; Kreutz, K.J.; Wake, C.P.; Naftz, D.L.; Frape, S.K.

2000-01-01

Chlorine-36 (36Cl) concentrations, 36Cl/Cl ratios, and 36Cl fluxes in ice-core samples collected from the Upper Fremont Glacier (UFG) in the Wind River Mountain Range, Wyoming, United States and the Nangpai Gosum Glacier (NGG) in the Himalayan Mountains, Nepal, were determined and compared with published results from the Dye-3 ice-core drilling site on the Greenland Ice Sheet. Cesium-137 (137Cs) concentrations in the NGG also were determined. The background fluxes for 36Cl for each glacial site were similar: (1.6??0.3)??10-2 atoms/cm2 s for the UFG samples, (0.7??0.1)??10-2 atoms/cm2 s for the NGG samples, and (0.4??0.1)??10-2 atoms/cm2 s for the Dye-3 samples. The 36Cl fluxes in ice that was deposited as snow during peak atmospheric nuclear weapon test (1957-1958) were (33??1)??10-2 atoms/cm2 s for the UFG site, (291??3)??10-2 atoms/cm2 s for the NGG site, and (124??5)??10-2 atoms/ cm2 s for the Dye-3 site. A weapon test period 137Cs concentration of 0.79??0.05 Bq/kg in the NGG ice core also was detected in the same section of ice that contained the largest 36Cl concentration. ?? 2000 Elsevier Science B.V. All rights reserved.

Mode change of millennial CO2 variability during the last glacial cycle associated with a bipolar marine carbon seesaw.

PubMed

Bereiter, Bernhard; Lüthi, Dieter; Siegrist, Michael; Schüpbach, Simon; Stocker, Thomas F; Fischer, Hubertus

2012-06-19

Important elements of natural climate variations during the last ice age are abrupt temperature increases over Greenland and related warming and cooling periods over Antarctica. Records from Antarctic ice cores have shown that the global carbon cycle also plays a role in these changes. The available data shows that atmospheric CO(2) follows closely temperatures reconstructed from Antarctic ice cores during these variations. Here, we present new high-resolution CO(2) data from Antarctic ice cores, which cover the period between 115,000 and 38,000 y before present. Our measurements show that also smaller Antarctic warming events have an imprint in CO(2) concentrations. Moreover, they indicate that during Marine Isotope Stage (MIS) 5, the peak of millennial CO(2) variations lags the onset of Dansgaard/Oeschger warmings by 250 ± 190 y. During MIS 3, this lag increases significantly to 870 ± 90 y. Considerations of the ocean circulation suggest that the millennial variability associated with the Atlantic Meridional Overturning Circulation (AMOC) undergoes a mode change from MIS 5 to MIS 4 and 3. Ocean carbon inventory estimates imply that during MIS 3 additional carbon is derived from an extended mass of carbon-enriched Antarctic Bottom Water. The absence of such a carbon-enriched water mass in the North Atlantic during MIS 5 can explain the smaller amount of carbon released to the atmosphere after the Antarctic temperature maximum and, hence, the shorter lag. Our new data provides further constraints for transient coupled carbon cycle-climate simulations during the entire last glacial cycle.

Ice core evidence for extensive melting of the greenland ice sheet in the last interglacial.

PubMed

Koerner, R M