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  • 1
    Publication Date: 2021-03-18
    Description: The quantitative reconstruction of past seawater salinity has yet to be achieved and the search for a direct and independent salinity proxy is ongoing. Recent culture and field studies show a significant positive correlation of Na/Ca with salinity in benthic and planktonic foraminiferal calcite. For accurate paleoceanographic reconstructions, consistent and reliable calibrations are necessary, which are still missing. In order to assess the reliability of foraminiferal Na/Ca as a direct proxy for seawater salinity, this study presents electron microprobe Na/Ca data, measured on cultured specimens of Trilobatus sacculifer. The culture experiments were conducted over a wide salinity range of 26 to 45, while temperature was kept constant. To further understand potential controlling factors of Na incorporation, measurements were also performed on foraminifera cultured at various temperatures in the range of 19.5 °C to 29.5 °C under constant salinity conditions. Foraminiferal Na/Ca ratios positively correlate with seawater salinity (Na/Caforam = 0.97 + 0.115 ⋅ Salinity, R = 0.97, p 〈 0.005). Temperature on the other hand exhibits no statistically significant relationship with Na/Ca ratios indicating salinity to be the dominant factor controlling Na incorporation. The culturing results are corroborated by measurements on T. sacculifer from Caribbean and Gulf of Guinea surface sediments. In conclusion, planktonic foraminiferal Na/Ca can be applied as a reliable proxy for reconstructing sea surface salinities, albeit species-specific calibrations might be necessary.
    Type: Article , PeerReviewed
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  • 2
    Publication Date: 2013-10-28
    Description: About 30% of the anthropogenically released CO2 is taken up by the oceans; such uptake causes surface ocean pH to decrease and is commonly referred to as ocean acidification (OA). Foraminifera are one of the most abundant groups of marine calcifiers, estimated to precipitate ca. 50 % of biogenic calcium carbonate in the open oceans. We have compiled the state of the art literature on OA effects on foraminifera, because the majority of OA research on this group was published within the last three years. Disparate responses of this important group of marine calcifiers to OA were reported, highlighting the importance of a process-based understanding of OA effects on foraminifera. We cultured the benthic foraminifer Ammonia sp. under a range of carbonate chemistry manipulation treatments to identify the parameter of the carbonate system causing the observed effects. This parameter identification is the first step towards a process-based understanding. We argue that [CO32−] is the parameter affecting foraminiferal size-normalized weights (SNWs) and growth rates. Based on the presented data, we can confirm the strong potential of Ammonia sp. foraminiferal SNW as a [CO32−] proxy.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
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  • 3
    Publication Date: 2022-01-31
    Description: Sea surface salinity is one of the most important parameters to reconstruct in paleoclimatology, reflecting amongst others the hydrological cycle, paleo-density, ice volume, and regional and global circulation of water masses. Recent culture studies and a Red Sea field study revealed a significant positive relation between salinity and Na incorporation within benthic and planktonic foraminiferal shells. However, these studies reported varying partitioning of Na between and within the same species. The latter could be associated with ontogenetic variations, most likely spine loss. Varying Na concentrations were observed in different parts of foraminiferal shells, with especially spines and regions close to the primary organic sheet being enriched in Na. In this study, we unravel the Na composition of different components of the planktonic foraminiferal shell wall using Electron Probe Micro Analysis (EPMA) and solution-ICP-MS. A model is presented to interpret EPMA data for spines and spine bases to quantitatively assess differences in composition and contribution to whole shell Na/Ca signals. The same model can also be applied to other spatial inhomogeneities observed in foraminiferal shell chemistry, like elemental (e.g. Mg, Na, S) banding and/or hotspots. The relative contribution of shell calcite, organic linings, spines and spine bases to whole shell Na chemistry is considered quantitatively. This study shows that whereas the high Na areas may be susceptible to taphonomy, the Na chemistry of the shell itself seems relatively robust. Comparing both shell and spine Na/Ca values with salinity shows that shell chemistry records salinity, albeit with a very modest slope.
    Type: Article , PeerReviewed
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  • 4
    Publication Date: 2024-02-07
    Description: A new matrix-matched reference material has been developed – NFHS-2-NP (NIOZ Foraminifera House Standard-2-Nano-Pellet) – with element mass fractions, and isotope ratios resembling that of natural foraminiferal calcium carbonate. A 180–355 µm size fraction of planktic foraminifera was milled to nano-particles and pressed to pellets. We report reference and information values for mass fractions of forty-six elements measured by six laboratories as well as for 87Sr/86Sr (three laboratories), δ13C, δ18O (five laboratories), and 206,207,208Pb/204Pb isotope ratios (one laboratory) determined by ICP-MS, ICP-OES, MC-ICP-MS, IRMS, WD-XRF and TIMS. Inter- and intra-pellet elemental homogeneity was tested using multiple LA-ICP-MS analyses in two laboratories applying spot sizes of 60 and 70 µm. The LA-ICP-MS results for most of the elements relevant as proxies for palaeoclimate research show RSD values 〈 3%, demonstrating a satisfactory homogeneous composition. Homogeneity of 87Sr/86Sr ratios of the pellet was verified by repeated LA-MC-ICP-MS by two laboratories. Information values are reported for Pb isotope ratios and δ13C, δ18O values. The homogeneity for these isotope systems remains to be tested by LA-MC-ICP-MS and SIMS. Overall, our results confirm the suitability of NFHS-2-NP for calibration or monitoring the quality of in situ geochemical techniques.
    Type: Article , PeerReviewed
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