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  • 1
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    PANGAEA
    In:  Supplement to: Nomura, Daiki; Assmy, Philipp; Nehrke, Gernot; Granskog, Mats A; Fischer, Michael; Dieckmann, Gerhard S; Fransson, Agneta; Hu, Yubin; Schnetger, Bernhard (2013): Characterization of ikaite (CaCO3 6H2O) crystals in first-year Arctic sea ice north of Svalbard. Annals of Glaciology, 54(62), 125-131, https://doi.org/10.3189/2013AoG62A034
    Publication Date: 2023-10-28
    Description: We identified ikaite crystals (CaCO3 · 6H2O) and examined their shape and size distribution in first-year Arctic pack ice, overlying snow and slush layers during the spring melt onset north of Svalbard. Additional measurements of total alkalinity (TA) were made for melted snow and sea-ice samples. Ikaite crystals were mainly found in the bottom of the snowpack, in slush and the surface layers of the sea ice where the temperature was generally lower and salinity higher than in the ice below. Image analysis showed that ikaite crystals were characterized by a roughly elliptical shape and a maximum caliper diameter of 201.0±115.9 µm (n = 918). Since the ice-melting season had already started, ikaite crystals may already have begun to dissolve, which might explain the lack of a relationship between ikaite crystal size and sea-ice parameters (temperature, salinity, and thickness of snow and ice). Comparisons of salinity and TA profiles for melted ice samples suggest that the precipitation/dissolution of ikaite crystals occurred at the top of the sea ice and the bottom of the snowpack during ice formation/melting processes.
    Keywords: Priority Programme 1158 Antarctic Research with Comparable Investigations in Arctic Sea Ice Areas; SPP1158
    Type: Dataset
    Format: application/zip, 3 datasets
    Location Call Number Limitation Availability
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  • 2
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    Unknown
    PANGAEA
    In:  Supplement to: Fischer, Michael; Thomas, David N; Krell, Andreas; Nehrke, Gernot; Göttlicher, Jörg; Norman, Marc D; Meiners, Klaus M; Riaux-Gobin, C; Dieckmann, Gerhard S (2012): Quantification of ikaite in Antarctic sea ice. Antarctic Science, 25(03), 421-432, https://doi.org/10.1017/S0954102012001150
    Publication Date: 2023-10-28
    Description: Calcium carbonate 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, although it is hypothesized that high quantities of dissolved organic matter and/or phosphate (common in sea ice) may inhibit its formation. In this quantitative study of hydrous calcium carbonate as ikaite, sea ice cores and brine samples were collected from pack and land fast sea ice between September and December 2007 during two expeditions, one in the East Antarctic sector and the other off Terre Adélie. Samples were analysed for CaCO3, salinity, dissolved organic carbon/nitrogen, inorganic phosphate, and total alkalinity. No relationship between these parameters and CaCO3 precipitation was evident. Ikaite was found mostly in the uppermost layers of sea ice with maximum concentrations of up to 126 mg ikaite per litre melted sea ice being measured, although both the temporal and horizontal spatial distributions of ikaite were highly heterogeneous. The precipitate was also found in the snow on top of the sea ice at some of the sampling locations.
    Keywords: Priority Programme 1158 Antarctic Research with Comparable Investigations in Arctic Sea Ice Areas; SPP1158
    Type: Dataset
    Format: application/zip, 3 datasets
    Location Call Number Limitation Availability
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  • 3
    Publication Date: 2024-03-19
    Keywords: ANT-XXIX/6; ANT-XXIX/6_HELI200713-1; ANT-XXIX/6_HELI200713-2; Comment; Comment 2 (continued); DATE/TIME; Device type; Event label; HELI; Helicopter; ICE; Ice station; Investigator; Latitude of event; Lazarev Sea; Longitude of event; Polarstern; PS81/486-1; PS81/488-2; PS81/489-2; PS81/493-2; PS81/496-1; PS81/500-5; PS81/503-2; PS81/506-1; PS81/515-1; PS81/517-2; PS81 AWECS; Sample code/label; Weddell Sea
    Type: Dataset
    Format: text/tab-separated-values, 1200 data points
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  • 4
    Publication Date: 2019-07-17
    Description: Calcium carbonate 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, although it is hypothesized that high quantities of dissolved organic matter and/or phosphate (common in sea ice) may inhibit its formation. In this quantitative study of hydrous calcium carbonate as ikaite, sea ice cores and brine samples were collected from pack and land fast sea ice between September and December 2007 during two expeditions, one in the East Antarctic sector and the other off Terre Ade´lie. Samples were analysed for CaCO3, salinity, dissolved organic carbon/nitrogen, inorganic phosphate, and total alkalinity. No relationship between these parameters and CaCO3 precipitation was evident. Ikaite was found mostly in the uppermost layers of sea ice with maximum concentrations of up to 126 mg ikaite per litre melted sea ice being measured, although both the temporal and horizontal spatial distributions of ikaite were highly heterogeneous. The precipitate was also found in the snow on top of the sea ice at some of the sampling locations.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 5
    Publication Date: 2017-06-14
    Description: Ikaite (CaCO3�6H2O) has recently been discovered in sea ice, providing first direct evidence of CaCO3 precipitation in sea ice. However, the impact of ikaite precipitation on phosphate (PO4) concentration has not been considered so far. Experiments were set up at pH from 8.5 to 10.0, salinities from 0 to 105, temperatures from 24°C to 0°C, and PO4 concentrations from 5 to 50 mmol kg-1 in artificial sea ice brine so as to understand how ikaite precipitation affects the PO4 concentration in sea ice under different conditions. Our results show that PO4 is coprecipitated with ikaite under all experimental conditions. The amount of PO4 removed by ikaite precipitation increases with increasing pH. Changes in salinity (S 〉=35) as well as temperature have little impact on PO4 removal by ikaite precipitation. The initial PO4 concentration affects the PO4 coprecipitation. These findings may shed some light on the observed variability of PO4 concentration in sea ice.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 6
    Publication Date: 2019-07-17
    Description: Data pertaining to environmental conditions, sympagic (sea ice) microalgal dynamics and particle flux were collected before the spring ice break-up 2001 in Pierre Lejay Bay, adjacent to the Dumont d'Urville Station, Petrel Island, East Antarctica. An array of two multiple sediment traps and a current meter was deployed for five weeks, from 8 November to 6 December 2001. The sea-ice chlorophyll a and particulate organic carbon (POC) averaged 0.6 mg l−1 (30 mg m−2) and 20 mg l−1 (1 g m−2) near the coast. The POC export flux that reached a maximum of 79 mg m−2 d−1 during the study period was high compared to the one for the Weddell Sea. The flux was homogeneous from the surface to 47 m depth and increased sharply 33 days before the effective ice break-up. A north-western progressive vector of currents (i.e., Lagrangian drift) in the sub-ice surface waters was demonstrated. Bottom ice, platelet ice and under-ice water at 5 m were characterized by differences in colonization and short-term succession of microalgae.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 7
    Publication Date: 2019-07-17
    Description: This study investigated the incorporation of DOM from seawater into 〉2 day-old sea ice in tanks filled with seawater alone or amended with DOM extracted from the microalga, Chlorella vulgaris. Optical properties, including chromophoric DOM (CDOM) absorption and fluorescence, as well as concentrations of dissolved organic carbon (DOC), dissolved organic nitrogen (DON), dissolved carbohydrates (dCHOs) and dissolved uronic acids (dUAs) were measured. Enrichment factors (EFs), calculated from salinity-normalized concentrations of DOM in bulk ice, brine and frost flowers relative to under-ice water, were generally 〉1. The enrichment factors varied for different DOM fractions: EFs were the lowest for humic-like DOM (1.0–1.39) and highest for amino acid-like DOM (1.10–3.94). Enrichment was generally highest in frost flowers with there being less enrichment in bulk ice and brine. Size exclusion chromatography indicated that there was a shift towards smaller molecules in the molecular size distribution of DOM in the samples collected from newly formed ice compared to seawater. Spectral slope coefficients did not reveal any consistent differences between seawater and ice samples. We conclude that DOM is incorporated to sea ice relatively more than inorganic solutes during initial formation of sea ice and the degree of the enrichment depends on the chemical composition of DOM
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 8
    Publication Date: 2014-07-30
    Description: Ikaite (CaCO3·6H2O) has only recently been discovered in sea ice, in a study that also provided first direct evidence of CaCO3 precipitation in sea ice. However, little is as yet known about the impact of physico-chemical processes on ikaite precipitation in sea ice. Our study focused on how the changes in pH, salinity, temperature and phosphate (PO4) concentration affect the precipitation of ikaite. Experiments were set up at pH from 8.5 to 10.0, salinities from 0 to 105 (in both artificial seawater (ASW) and NaCl medium), temperatures from 0 to −4 °C andPO4 concentrations from0 to 50 μmol kg−1. The results show that in ASW, calcium carbonate was precipitated as ikaite under all conditions. In the NaCl medium, the precipitates were ikaite in the presence of PO4 and vaterite in the absence of PO4. The onset time (τ) at which ikaite precipitation started, decreased nonlinearly with increasing pH. In ASW, τ increased with salinity. In the NaCl medium, τ first increased with salinity up to salinity 70 and subsequently decreased with a further increase in salinity; it was longer in ASW than in the NaCl medium under the same salinity. τ did not vary with temperature or PO4 concentration. These results indicate that ikaite is very probably the only phase of calcium carbonate formed in sea ice. PO4 is not, as previously postulated, crucial for ikaite formation in sea ice. The change in pH and salinity is the controlling factor for ikaite precipitation in sea ice. Within the ranges investigated in this study, temperature and PO4 concentration do not have a significant impact on ikaite precipitation.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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  • 9
    Publication Date: 2019-07-17
    Description: The structure of sea-ice bacterial communities is frequently different from that in seawater. Bacterial entrainment in sea ice has been studied with traditional microbiological, bacterial abundance, and bacterial production methods. However, the dynamics of the changes in bacterial communities during the transition from open water to frozen sea ice is largely unknown. Given previous evidence that the nutritional status of the parent water may affect bacterial communities during ice formation, bacterial succession was studied in under ice water and sea ice in two series of mesocosms: the first containing seawater from the North Sea and the second containing seawater enriched with algal-derived dissolved organic matter (DOM). The composition and dynamics of bacterial communities were investigated with terminal restriction fragment length polymorphism (T-RFLP), and cloning alongside bacterial production (thymidine and leucine uptake) and abundance measurements (measured by flow cytometry). Enriched and active sea-ice bacterial communities developed in ice formed in both unenriched and DOM-enriched seawater (0–6 days). γ-Proteobacteria dominated in the DOM-enriched samples, indicative of their capability for opportunistic growth in sea ice. The bacterial communities in the unenriched waters and ice consisted of the classes Flavobacteria, α- and γ-Proteobacteria, which are frequently found in natural sea ice in polar regions. Furthermore, the results indicate that seawater bacterial communities are able to adapt rapidly to sudden environmental changes when facing considerable physicochemical stress such as the changes in temperature, salinity, nutrient status, and organic matter supply during ice formation.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , peerRev
    Format: application/pdf
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  • 10
    Publication Date: 2019-07-17
    Description: A large-scale geographical study of the ice pack in the seasonal ice zone of the Weddell Sea, Antarctica, took place from September to October 2006. Sea ice brines with a salinity greater than 58 and temperature lower than -3.6oC were sampled from 22 ice stations. The brines had large deficits in total alkalinity and in the concentrations of the major dissolved macronutrients (total dissolved inorganic carbon, nitrate, and soluble reactive phosphorus) relative to their concentrations in the surface oceanic water and conservative behaviour during seawater freezing. The concentration deficits were related to the dissolved inorganic carbon-consuming processes of photosynthesis, CaCO3 precipitation, and CO2 degassing. The largest concentration deficits in total dissolved inorganic carbon were found to be associated with CaCO3 precipitation and CO2 degassing, because the magnitude of the photosynthesis-induced concentration deficit in total dissolved inorganic carbon is controlled by the size of the inorganic nutrient pool, which can be limited in sea ice by its openness to exchange with the surrounding oceanic water.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , peerRev
    Format: application/pdf
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