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  • 1
    Type of Medium: Online Resource
    Pages: Online-Ressource (88 Seiten, 3,3 MB) , Diagramme, Karten
    Series Statement: Berichte aus dem Institut für Meereskunde an der Christian-Albrechts-Universität Kiel 238
    Language: English
    Note: Zusammenfassung in deutscher und englischer Sprache
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  • 2
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    PANGAEA
    In:  Supplement to: Croot, Peter L; Baars, Oliver; Streu, Peter (2011): The distribution of dissolved zinc in the Atlantic sector of the Southern Ocean. Deep Sea Research Part II: Topical Studies in Oceanography, 58(25-26), 2707-2719, https://doi.org/10.1016/j.dsr2.2010.10.041
    Publication Date: 2023-10-28
    Description: The distribution of dissolved zinc (Zn) was investigated in the Atlantic sector of the Southern Ocean in the austral autumn of 2008 as part of the IPY GEOTRACES expedition ZERO & DRAKE. Research focused on transects across the major frontal systems along the Zero Meridian and across the Drake Passage. There was a strong gradient in surface zinc concentrations observed across the Antarctic Polar Front along both transects and high zinc levels were found in surface waters throughout the Southern Ocean. Vertical profiles for dissolved Zinc showed the presence of local minima and maxima in the upper 200 m consistent with significant uptake by phytoplankton and release by zooplankton grazing, respectively. Highest deep water zinc concentrations were found in the centre of the Weddell Gyre associated with Central Intermediate Water (CIW), a water mass which is depleted in O2, elevated in CO2 and is regionally a CFC minimum. Our data suggests that the remineralization of sinking particles is a key control on the distribution of Zn in the Southern Ocean. Disappearance ratios of zinc to phosphate (Zn:P) in the upper water column increased southwards along both transects and based on laboratory studies they suggest slower growth rates of phytoplankton due to iron or light limitation. Zinc and silicate were strongly correlated throughout the study region but the disappearance ratio (Zn:Si) was relatively uniform overall except for the region close to the ice edge on the Zero Meridian.
    Keywords: ANT-XXIV/3; Bottle number; CTD/Rosette, ultra clean; CTD-UC; Date/Time of event; DEPTH, water; Drake Passage; Element analyser AAS, graphite furnace, Perkin-Elmer 4100 ZL; Elevation of event; Event label; GEOTRACES; Global marine biogeochemical cycles of trace elements and their isotopes; Latitude of event; Longitude of event; Nitrate and Nitrite; Nitrite; Phosphate; Polarstern; Pressure, water; Priority Programme 1158 Antarctic Research with Comparable Investigations in Arctic Sea Ice Areas; PS71; PS71/103-1; PS71/104-2; PS71/107-3; PS71/113-3; PS71/119-1; PS71/128-1; PS71/131-5; PS71/141-1; PS71/150-2; PS71/167-1; PS71/230-6; PS71/236-3; PS71/241-6; PS71/249-3; Salinity; Scotia Sea, southwest Atlantic; Silicate; South Atlantic Ocean; SPP1158; Temperature, water; Weddell Sea; Zinc, dissolved
    Type: Dataset
    Format: text/tab-separated-values, 1184 data points
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  • 3
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    PERGAMON-ELSEVIER SCIENCE LTD
    In:  EPIC3Deep-Sea Research Part II-Topical Studies in Oceanography, PERGAMON-ELSEVIER SCIENCE LTD, 58(25-26), pp. 2707-2719, ISSN: 0967-0645
    Publication Date: 2019-07-17
    Description: The distribution of dissolved zinc (Zn) was investigated in the Atlantic sector of the Southern Ocean in the austral autumn of 2008 as part of the IPY GEOTRACES expedition ZERO & DRAKE. Research focused on transects across the major frontal systems along the Zero Meridian and across the Drake Passage. There was a strong gradient in surface zinc concentrations observed across the Antarctic Polar Front along both transects and high zinc levels were found in surface waters throughout the Southern Ocean. Vertical profiles for dissolved Zinc showed the presence of local minima and maxima in the upper 200 m consistent with significant uptake by phytoplankton and release by zooplankton grazing, respectively. Highest deep water zinc concentrations were found in the centre of the Weddell Gyre associated with Central Intermediate Water (CIW), a water mass which is depleted in O2, elevated in CO2 and is regionally a CFC minimum. Our data suggests that the remineralization of sinking particles is a key control on the distribution of Zn in the Southern Ocean. Disappearance ratios of zinc to phosphate (Zn:P) in the upper water column increased southwards along both transects and based on laboratory studies they suggest slower growth rates of phytoplankton due to iron or light limitation. Zinc and silicate were strongly correlated throughout the study region but the disappearance ratio (Zn:Si) was relatively uniform overall except for the region close to the ice edge on the Zero Meridian.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 4
    Publication Date: 2021-04-23
    Description: Certification of trace metals in seawater certified reference materials (CRMs) NASS-7 and CASS-6 is described. At the National Research Council Canada (NRC), column separation was performed to remove the seawater matrix prior to the determination of Cd, Cr, Cu, Fe, Pb, Mn, Mo, Ni, U, V, and Zn, whereas As was directly measured in 10-fold diluted seawater samples, and B was directly measured in 200-fold diluted seawater samples. High-resolution inductively coupled plasma mass spectrometry (HR-ICPMS) was used for elemental analyses, with double isotope dilution for the accurate determination of B, Cd, Cr, Cu, Fe, Pb, Mo, Ni, U, and Zn in seawater NASS-7 and CASS-6, and standard addition calibration for As, Co, Mn, and V. In addition, all analytes were measured using standard addition calibration with triple quadrupole (QQQ)-ICPMS to provide a second set of data at NRC. Expert laboratories worldwide were invited to contribute data to the certification of trace metals in NASS-7 and CASS-6. Various analytical methods were employed by participants including column separation, co-precipitation, and simple dilution coupled to ICPMS detection or flow injection analysis coupled to chemiluminescence detection, with use of double isotope dilution calibration, matrix matching external calibration, and standard addition calibration. Results presented in this study show that majority of laboratories have demonstrated their measurement capabilities for the accurate determination of trace metals in seawater. As a result of this comparison, certified/reference values and associated uncertainties were assigned for 14 elements in seawater CRMs NASS-7 and CASS-6, suitable for the validation of methods used for seawater analysis.
    Type: Article , PeerReviewed
    Format: text
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  • 5
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    Elsevier
    In:  Deep Sea Research Part I: Oceanographic Research Papers, 40 (6). pp. 1155-1168.
    Publication Date: 2018-03-05
    Description: Particulate fluxes of aluminium, cadmium, cobalt, copper, iron, manganese, nickel, phosphorus, lead, vanadium and zinc in the northeast subtropical Atlantic Ocean have been determined from sediment trap samples collected between 1 December 1986 and 30 April 1987 at 1020 and 4120 m below the ocean surface. The fluxes of most elements (except Cd and P) show small variations between the different layers, and are closely associated with the vertical transport of aluminium. Elemental composition and flux rates suggest that aerosol loadings from northeast trade winds are the major contributor of these elements to depositing material. Extremely low fluxes of copper, lead and zinc also indicate that anthropogenic perturbations are of insignificant importance in this region.
    Type: Article , PeerReviewed
    Format: text
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  • 6
    Publication Date: 2021-04-23
    Description: Dissolved iron (DFe) concentrations in oxygen minimum zones (OMZs) of Eastern Boundary Upwelling Systems are enhanced as a result of high supply rates from anoxic sediments. However, pronounced variations in DFe concentrations in anoxic coastal waters of the Peruvian OMZ indicate that there are factors in addition to dissolved oxygen concentrations (O2) that control Fe cycling. Our study demonstrates that sediment-derived reduced Fe (Fe(II)) forms the main DFe fraction in the anoxic/euxinic water column off Peru, which is responsible for DFe accumulations of up to 200 nmol L-1. Lowest DFe values were observed in anoxic shelf waters in the presence of nitrate and nitrite. This reflects oxidation of sediment-sourced Fe(II) associated with nitrate/nitrite reduction and subsequent removal as particulate Fe(III) oxyhydroxides. Unexpectedly, the highest DFe levels were observed in waters with elevated concentrations of hydrogen sulfide (up to 4 µmol L-1) and correspondingly depleted nitrate/nitrite concentrations (〈0.18 µmol L-1). Under these conditions, Fe removal was reduced through stabilization of Fe(II) as aqueous iron sulfide (FeSaqu) which comprises complexes (e.g., FeSH+) and clusters (e.g., Fe2S2|4H2O). Sulfidic events on the Peruvian shelf consequently enhance Fe availability, and may increase in frequency in future due to projected expansion and intensification of OMZs.
    Type: Article , PeerReviewed
    Format: text
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  • 7
    Publication Date: 2020-02-18
    Description: The deposition of atmospheric dust is the primary process supplying trace elements abundant in crustal rocks (e.g. Al, Mn and Fe) to the surface ocean. Upon deposition, the residence time in surface waters for each of these elements differs according to their chemical speciation and biological utilization. Presently, however, the chemical and physical processes occurring after atmospheric deposition are poorly constrained, principally because of the difficulty in following natural dust events in situ. In the present work we examined the temporal changes in the biogeochemistry of crustal metals (in particular Al, Mn and Fe) after an artificial dust deposition event. The experiment was contained inside trace metal clean mesocosms (0–12.5 m depths) deployed in the surface waters of the northwestern Mediterranean, close to the coast of Corsica within the frame of the DUNE project (a DUst experiment in a low Nutrient, low chlorophyll Ecosystem). Two consecutive artificial dust deposition events, each mimicking a wet deposition of 10 g m−2 of dust, were performed during the course of this DUNE-2 experiment. The changes in dissolved manganese (Mn), iron (Fe) and aluminum (Al) concentrations were followed immediately after the seeding with dust and over the following week. The Mn, Fe and Al inventories and loss or dissolution rates were determined. The evolution of the inventories after the two consecutive additions of dust showed distinct behaviors for dissolved Mn, Al and Fe. Even though the mixing conditions differed from one seeding to the other, Mn and Al showed clear increases directly after both seedings due to dissolution processes. Three days after the dust additions, Al concentrations decreased as a consequence of scavenging on sinking particles. Al appeared to be highly affected by the concentrations of biogenic particles, with an order of magnitude difference in its loss rates related to the increase of biomass after the addition of dust. In the case of dissolved Fe, it appears that the first dust addition resulted in a decrease as it was scavenged by sinking dust particles, whereas the second seeding induced dissolution of Fe from the dust particles due to the excess Fe binding ligand concentrations present at that time. This difference, which might be related to a change in Fe binding ligand concentration in the mesocosms, highlights the complex processes that control the solubility of Fe. Based on the inventories at the mesocosm scale, the estimations of the fractional solubility of metals from dust particles in seawater were 1.44 ± 0.19% and 0.91 ± 0.83% for Al and 41 ± 9% and 27 ± 19% for Mn for the first and the second dust addition. These values are in good agreement with laboratory-based estimates. For Fe no fractional solubility was obtained after the first seeding, but 0.12 ± 0.03% was estimated after the second seeding. Overall, the trace metal dataset presented here makes a significant contribution to enhancing our knowledge on the processes influencing trace metal release from Saharan dust and the subsequent processes of bio-uptake and scavenging in a low nutrient, low chlorophyll area
    Type: Article , PeerReviewed
    Format: text
    Format: archive
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  • 8
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    ASLO (Association for the Sciences of Limnology and Oceanography)
    In:  Limnology and Oceanography, 57 (3). pp. 684-697.
    Publication Date: 2019-07-09
    Description: Iron solubility (cFeS) ranged from 0.4 to 1.5 nmol L−1, decreasing from south to north in three different Southern Ocean zones (the Coastal Zone, the Antarctic Zone, and the Polar Frontal Zone plus the Subantarctic Zone). This decrease was at times correlated with an increase in temperature. Organic Fe solubility (cFeS,org), which was obtained by subtracting from total measured Fe solubility the solubility of inorganic species of iron (Fe) at the measurement temperature (20°C), ranged from 0.3 to 1.3 nmol L−1, representing an average of 32 ± 14% of the concentration of ligands in the dissolved size fraction as determined via competitive ligand exchange–absorptive cathodic stripping voltammetry (barring a handful of extremely high values from a transect run to the east of Prydz Bay). Values of cFeS were mainly lower than the predicted value for inorganic Fe solubility at the in situ temperature. Total in situ Fe solubility (cFeS,adj) was therefore estimated by adjusting for inorganic Fe solubility at in situ temperatures (between −2°C and +18°C). Because in situ temperatures in the Antarctic Circumpolar Current were mostly lower than +3°C, such cFeS,adj values, ranging from 0.5 to 1.8 nmol L−1, were roughly twice as large as cFeS,org. The adjustment relies heavily on model calculations of inorganic Fe solubility but, if correct, indicates that the bulk of the solubility of Fe in the cold waters of the Southern Ocean is tied to the solubility of inorganic Fe rather than to Fe ligands in the soluble size fraction.
    Type: Article , PeerReviewed
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  • 9
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    American Society of Limnology and Oceanography
    In:  Limnology and Oceanography: Methods, 11 . pp. 187-201.
    Publication Date: 2019-09-24
    Description: Vivaspin6® ultrafiltration units with molecular weight “cut-off” membranes of 5, 10, 30, 50, and 100 kDa were used together to examine the size distribution of newly formed iron (Fe) colloids in natural seawater samples and in the presence of several different Fe chelators with varying Fe binding strength. Artificial Fe chelators, such as TAC, and 2 kDG, when added at equimolar levels to Fe, supported the formation of a continuum of Fe-ligand colloids between 5 and 100 kDa. More than 90% of the added 55Fe in these solutions occurred in Fe aggregates/particles larger than 100 kDa. The strong siderophore DFO held the majority of the added 55Fe in the “truly” soluble fraction ≤ 5 kDa, whereas 90% of 55Fe added to UV-irradiated seawater was converted into Fe colloids with a size between 50 to 100 kDa (5–6 nm). Membranes with ≥ 10 kDa showed similar “cut-off” properties on natural seawater samplescollected in the water column off the Peruvian coast. Fe solubility determined with these membranes was approximately six times greater than Fe solubility determined with the 5 kDa membrane and the 0.02 μm syringe filters. This suggests that a seamless size continuum of organic chelators (≤5 kDa–10 kDa) is present in these seawaters and that estimates of ligand production based on 0.02 μm Anotop solubility experiments underestimates the abundance of soluble/colloidal ligands. Regarding these results, we recommend the use of Vivaspin 5 kDa membranes to separate the “truly” soluble from the colloidal Fe fraction.
    Type: Article , PeerReviewed
    Format: text
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  • 10
    Publication Date: 2012-02-23
    Type: Conference or Workshop Item , NonPeerReviewed
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