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  • 2010-2014  (141)
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  • 1
    In: Geology, Melville, NY : American Institute of Physics, 1973, 39(2011), 11, Seite 1039-1042, 1943-2682
    In: volume:39
    In: year:2011
    In: number:11
    In: pages:1039-1042
    Materialart: Online-Ressource
    Seiten: graph. Darst
    ISSN: 1943-2682
    Sprache: Englisch
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Publikationsdatum: 2018-08-15
    Beschreibung: One of the key activities during the initial phase of the international GEOTRACES program was an extensive international intercalibration effort, to ensure that results for a range of trace elements and isotopes (TEIs) from different cruises and from different laboratories can be compared in a meaningful way. Here we present the results from the intercalibration efforts on neodymium isotopes and rare earth elements in seawater and marine particles. Fifteen different laboratories reported results for dissolved 143Nd/144Nd ratios in seawater at three different locations (BATS 15 m, BATS 2000 m, SAFe 3000 m), with an overall agreement within 47 to 57 ppm (2σ standard deviation of the mean). A similar agreement was found for analyses of an unknown pure Nd standard solution carried out by 13 laboratories (56 ppm), indicating that mass spectrometry is the main variable in achieving accurate and precise Nd isotope ratios. Overall, this result is very satisfactory, as the achieved precision is a factor of 40 better than the range of Nd isotopic compositions observed in the global ocean. Intercalibration for dissolved rare earth element concentrations (REEs) by six laboratories for two water depths at BATS yielded a reproducibility of 15% or better for all REE except Ce, which seems to be the most blank-sensitive REE. Neodymium concentrations from 12 laboratories show an agreement within 9%, reflecting the best currently possible reproducibility. Results for Nd isotopic compositions and REE concentrations on marine particles are inconclusive, and should be revisited in the future.
    Materialart: Article , PeerReviewed
    Format: text
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Publikationsdatum: 2017-05-10
    Beschreibung: Previous studies have demonstrated the potential for the Li content of coral aragonite to record information about environmental conditions, but no detailed study of tropical corals exists. Here we present the Li and Mg to Ca ratios at a bimonthly to monthly resolution over 25 years in two modern Porites corals, the genus most often used for paleoclimate reconstructions in the tropical Indo-Pacific. A strong relationship exists between coral Li/Ca and locally measured SST, indicating that coral Li/Ca can be used to reconstruct tropical SST variations. However, Li/Ca ratios of the skeleton deposited during 1979-1980 do not track local SST well and are anomalously high in places. The Mg/Ca ratios of this interval are also anomalously high, and we suggest Li/Ca can be used to reconstruct tropical SST only when Mg/Ca data are used to carefully screen for relatively rare biological effects. Mg/Li or Li/Mg ratios provide little advantage over Li/Ca ratios, except that the slope of the Li/Mg temperature relationship is more similar between the two corals. The Mg/Li temperature relationship for the coral that experienced a large temperature range is similar to that found for cold water corals and aragonitic benthic foraminifera in previous studies. The comparison with data from other biogenic aragonites suggests the relationship between Li/Mg and water temperature can be described by a single exponential relationship. Despite this hint at an overarching control, it is clear that biological processes strongly influence coral Li/Ca, and more calibration work is required before widely applying the proxy
    Materialart: Article , PeerReviewed
    Format: text
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  • 4
    Publikationsdatum: 2017-06-19
    Beschreibung: The radiogenic neodymium (Nd) isotope composition of foraminiferal shells provides a powerful archive to investigate past changes in sources and mixing of water masses. However, seawater Nd isotope ratios extracted from foraminiferal shells can be biased by contaminant phases such as organic matter, silicates, or ferromanganese coatings, the removal of which requires rigorous multiple step cleaning of the samples. Here we investigate the efficiency of Flow Through and batch cleaning methods to extract seawater Nd isotope compositions from planktonic foraminifera in a shelf setting in the Gulf of Guinea that is strongly influenced by riverine sediment inputs. Nd isotope analyses of reductively and oxidatively cleaned mono-specific planktonic foraminiferal samples and reductively cleaned mixed benthic foraminifera were complemented by analyses of non-reductively cleaned mono-specific planktonic foraminiferal samples, Fe–Mn coatings of de-carbonated bulk sediment leachates, and the residual detrital fraction of the same sediment. Al/Ca and Mn/Ca ratios of fully cleaned foraminiferal samples reveal indistinguishable levels of cleaning efficiency between the batch and the Flow Through methods and the Nd isotope compositions obtained from application of both methods are identical within error. Furthermore, non-reductively cleaned foraminiferal samples have the same Nd isotope composition as reductively cleaned foraminifera at our study sites. Close to the Niger River mouth the Nd isotope composition of the foraminifera agree with the seawater Nd isotope composition of nearby stations. Based on the combined extracted Nd isotope signatures and element to calcium ratios, as well as rare earth element distribution patterns, we infer that the planktonic foraminiferal Nd isotope signatures reflect bottom water/pore water signatures. The isotopic composition of the bulk de-carbonated sediment leachates (Fe–Mn coatings) differs significantly from the foraminiferal data at this site and probably reflects particles that acquired their ferromanganese/pre-formed pre-formed/ferromanganese coatings in nearby rivers. Therefore, in such river influenced shelf settings foraminiferal shells should be used to obtain unbiased bottom seawater signatures.
    Materialart: Article , PeerReviewed
    Format: text
    Format: text
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  • 5
    Publikationsdatum: 2017-09-26
    Beschreibung: Radiogenic isotopes of hafnium (Hf) and neodymium (Nd) are powerful tracers for water mass transport and trace metal cycling in the present and past oceans. However, due to the scarcity of available data the processes governing their distribution are not well understood. Here we present the first combined dissolved Hf and Nd isotope and concentration data from surface waters of the Atlantic sector of the Southern Ocean. The samples were collected along the Zero Meridian, in the Weddell Sea and in the Drake Passage during RV Polarstern expeditions ANTXXIV/3 and ANTXXIII/3 in the frame of the International Polar Year (IPY) and the GEOTRACES program. The general distribution of Hf and Nd concentrations in the region is similar. However, at the northernmost station located 200 km southwest of Cape Town a pronounced increase of the Nd concentration is observed, whereas the Hf concentration is minimal, suggesting much less Hf than Nd is released by the weathering of the South African Archean cratonic rocks. From the southern part of the Subtropical Front (STF) to the Polar Front (PF) Hf and Nd show the lowest concentrations (〈0.12 pmol/kg and 10 pmol/kg, respectively), most probably due to the low terrigenous flux in this area and efficient scavenging of Hf and Nd by biogenic opal. In the vicinity of landmasses the dissolved Hf and Nd isotope compositions are clearly labeled by terrigenous inputs. Near South Africa Nd isotope values as low as εNd = −18.9 indicate unradiogenic inputs supplied via the Agulhas Current. Further south the isotopic data show significant increases to εHf = 6.1 and εNd = −4.0 documenting exchange of seawater Nd and Hf with the Antarctic Peninsula. In the open Southern Ocean the Nd isotope compositions are relatively homogeneous (εNd ∼ −8 to −8.5) towards the STF, within the Antarctic Circumpolar Current, in the Weddell Gyre, and the Drake Passage. The Hf isotope compositions in the entire study area only show a small range between εHf = + 6.1 and +2.8 support Hf to be more readily released from young mafic rocks compared to old continental ones. The Nd isotope composition ranges from εNd = −18.9 to −4.0 showing Nd isotopes to be a sensitive tracer for the provenance of weathering inputs into surface waters of the Southern Ocean.
    Materialart: Article , PeerReviewed
    Format: text
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 6
    Publikationsdatum: 2019-09-23
    Beschreibung: Dissolved rare earth element (REE) concentrations and Nd isotope compositions were measured for surface waters and full water column profiles of the Gulf of Alaska (GoA), and compared to water mass properties and circulation in order to better understand the mechanisms controlling the input and transport of REEs in the ocean. The REEs display a typical open-ocean range of concentrations (i.e., La: 12-66 pM; Lu: 0.2-2.5 pM) and depth distributions (i.e., surface ocean depletion and enrichment with water depth). Nd isotope signatures are highly radiogenic, as expected for the North Pacific margin (ranging from -3.8 to +0.2 epsilon Nd). The most radiogenic values were found in the coastal waters but also in the cores of eddies, indicating efficient export of REEs from the margins and across the mixed layer. This is the first time that distinct Nd isotope distributions in near surface waters can be directly assigned to offshore eddy transport. A distinct mid-depth (similar to 2200 m) Nd isotope signal was found that most likely reflects advection of a water mass that formed through past down-welling in the Northern Pacific. Subsurface Nd isotope compositions appear to behave conservatively and can be explained through a REE distribution model proposed here. This model is based on multivariate analysis of the REEs and invokes two distinct "pools" of dissolved REEs: a "passive pool" complexed by carbonate ions, and a "bio-reactive pool" that is microbially manipulated. The latter "pool" is only significant in the upper water column and most likely reflects the indirect effects of microbial cycling of iron. Our model of the open ocean REE distribution contributes to explaining the conservative nature of Nd isotopes and provides a mechanism linking surface ocean and pore water REE dynamics
    Materialart: Article , PeerReviewed
    Format: text
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 7
    Publikationsdatum: 2017-06-19
    Beschreibung: The East Scotia subduction zone, located in the Atlantic sector of the Southern Ocean, hosts a number of hydrothermal sites in both back-arc and island-arc settings. High temperature (〉348 °C) ‘black smoker’ vents have been sampled at three locations along segments E2 and E9 of the East Scotia back-arc spreading ridge, as well as ‘white smoker’ (〈212 °C) and diffuse (〈28 °C) hydrothermal fluids from within the caldera of the Kemp submarine volcano. The composition of the endmember fluids (Mg = 0 mmol/kg) is markedly different, with pH ranging from 〈1 to 3.4, [Cl−] from ∼90 to 536 mM, [H2S] from 6.7 to ∼200 mM and [F−] from 35 to ∼1000 μM. All of the vent sites are basalt- to basaltic andesite-hosted, providing an ideal opportunity for investigating the geochemical controls on rare earth element (REE) behaviour. Endmember hydrothermal fluids from E2 and E9 have total REE concentrations ranging from 7.3 to 123 nmol/kg, and chondrite-normalised distribution patterns are either light REE-enriched (LaCN/YbCN = 12.8–30.0) with a positive europium anomaly (EuCN/Eu∗CN = 3.45–59.5), or mid REE-enriched (LaCN/NdCN = 0.61) with a negative Eu anomaly (EuCN/Eu∗CN = 0.59). By contrast, fluids from the Kemp Caldera have almost flat REE patterns (LaCN/YbCN = 2.1–2.2; EuCN/Eu∗CN = 1.2–2.2). We demonstrate that the REE geochemistry of fluids from the East Scotia back-arc spreading ridge is variably influenced by ion exchange with host minerals, phase separation, competitive complexation with ligands, and anhydrite deposition, whereas fluids from the Kemp submarine volcano are also affected by the injection of magmatic volatiles which enhances the solubility of all the REEs. We also show that the REE patterns of anhydrite deposits from Kemp differ from those of the present-day fluids, potentially providing critical information about the nature of hydrothermal activity in the past, where access to hydrothermal fluids is precluded.
    Materialart: Article , PeerReviewed
    Format: text
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 8
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    Unbekannt
    Integrated Ocean Drilling Program Management International, Inc.
    In:  Proceedings of the Integrated Ocean Drilling Program, 320/321 . Integrated Ocean Drilling Program Management International, Inc., Tokyo, Japan, Diverse Zählungen pp.
    Publikationsdatum: 2019-06-25
    Beschreibung: Integrated Ocean Drilling Program Expedition 320/321, "Pacific Equatorial Age Transect" (Sites U1331–U1338), was designed to recover a continuous Cenozoic record of the equatorial Pacific by coring above the paleoposition of the Equator at successive crustal ages on the Pacific plate. These sediments record the evolution of the equatorial climate system throughout the Cenozoic. As we gained more information about the past movement of plates and when in Earth's history "critical" climate events took place, it became possible to drill an age transect ("flow-line") along the position of the paleoequator in the Pacific, targeting important time slices where the sedimentary archive allows us to reconstruct past climatic and tectonic conditions. The Pacific Equatorial Age Transect (PEAT) program cored eight sites from the sediment surface to basement, with basalt aged between 53 and 18 Ma, covering the time period following maximum Cenozoic warmth, through initial major glaciations, to today. The PEAT program allows the reconstruction of extreme changes of the calcium carbonate compensation depth (CCD) across major geological boundaries during the last 53 m.y. A very shallow CCD during most of the Paleogene makes it difficult to obtain well-preserved carbonate sediments during these stratigraphic intervals, but Expedition 320 recovered a unique sedimentary biogenic sediment archive for time periods just after the Paleocene/Eocene boundary event, the Eocene cooling, the Eocene–Oligocene transition, the "one cold pole" Oligocene, the Oligocene–Miocene transition, and the middle Miocene cooling. Expedition 321, the second part of the PEAT program, recovered sediments from the time period roughly from 25 Ma forward, including sediments crossing the Oligocene/Miocene boundary and two major Neogene equatorial Pacific sediment sections. Together with older Deep Sea Drilling Project and Ocean Drilling Program drilling in the equatorial Pacific, we can delineate the position of the paleoequator and variations in sediment thickness from ~150°W to 110°W longitude.
    Materialart: Report , NonPeerReviewed
    Format: other
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 9
    facet.materialart.
    Unbekannt
    In:  [Poster] In: 11. International Conference on Paleoceanography, 01.-06.09.2013, Sigtes - Barcelona, Spain .
    Publikationsdatum: 2016-04-26
    Materialart: Conference or Workshop Item , NonPeerReviewed
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 10
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    Unbekannt
    In:  [Poster] In: 11. International Conference on Paleoceanography (ICP11) 2013, 01.-06.09.2013, Sitges - Barcelona, Spain .
    Publikationsdatum: 2016-04-26
    Materialart: Conference or Workshop Item , NonPeerReviewed
    Standort Signatur Einschränkungen Verfügbarkeit
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