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  • Copernicus GmbH  (18)
  • Biodiversity Research  (18)
  • 1
    In: Biogeosciences, Copernicus GmbH, Vol. 15, No. 20 ( 2018-10-26), p. 6315-6328
    Abstract: Abstract. Manganese geochemistry in deep-sea sediments is known to vary greatly over the first few centimeters, which overlaps the in-sediment depth habitats of several benthic foraminiferal species. Here we investigated manganese incorporation in benthic foraminiferal shell carbonate across a six-station depth transect in the Gulf of Lions, NW Mediterranean, to unravel the impacts of foraminiferal ecology and Mn pore water geochemistry. Over this transect water depth increases from 350 to 1987 m, while temperature (∼13 ∘C) and salinity (∼38.5) remained relatively constant. Manganese concentrations in the tests of living (rose bengal stained) benthic foraminiferal specimens of Hoeglundina elegans, Melonis barleeanus, Uvigerina mediterranea, and Uvigerina peregrina were measured using laser ablation inductively coupled mass spectrometry (laser ablation ICP-MS). Pore water manganese concentrations show a decrease from shallow to deeper waters, which corresponds to a generally decreasing organic-matter flux with water depth. Differences in organic-matter loading at the sediment–water interface affects oxygen penetration depth into the sediment and hence Mn pore water profiles. Mn ∕ Ca values for the investigated foraminiferal species reflect pore water geochemistry and species-specific microhabitat in the sediment. The observed degree of variability within a single species is in line with known ranges in depth habitat and gradients in redox conditions. Both the Mn ∕ Ca ratio and interspecific variability hence reflect past Mn cycling and related early diagenetic processes within the sediment, making this a potential tool for bottom-water oxygenation and organic-matter fluxes. Dynamics of both in-sediment foraminiferal depth habitats and Mn cycling, however, limit the application of such a proxy to settings with relatively stable environmental conditions.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
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  • 2
    In: Biogeosciences, Copernicus GmbH, Vol. 16, No. 10 ( 2019-05-20), p. 2115-2130
    Abstract: Abstract. Shell chemistry of foraminiferal carbonate proves to be useful in reconstructing past ocean conditions. A new addition to the proxy toolbox is the ratio of sulfur (S) to calcium (Ca) in foraminiferal shells, reflecting the ratio of SO42- to CO32- in seawater. When comparing species, the amount of SO42- incorporated, and therefore the S∕Ca of the shell, increases with increasing magnesium (Mg) content. The uptake of SO42- in foraminiferal calcite is likely connected to carbon uptake, while the incorporation of Mg is more likely related to Ca uptake since this element substitutes for Ca in the crystal lattice. The relation between S and Mg incorporation in foraminiferal calcite therefore offers the opportunity to investigate the timing of processes involved in Ca and carbon uptake. To understand how foraminiferal S∕Ca is related to Mg∕Ca, we analyzed the concentration and within-shell distribution of S∕Ca of three benthic species with different shell chemistry: Ammonia tepida, Bulimina marginata and Amphistegina lessonii. Furthermore, we investigated the link between Mg∕Ca and S∕Ca across species and the potential influence of temperature on foraminiferal S∕Ca. We observed that S∕Ca is positively correlated with Mg∕Ca on a microscale within specimens, as well as between and within species. In contrast, when shell Mg∕Ca increases with temperature, foraminiferal S∕Ca values remain similar. We evaluate our findings in the light of previously proposed biomineralization models and abiological processes involved during calcite precipitation. Although all kinds of processes, including crystal lattice distortion and element speciation at the site of calcification, may contribute to changes in either the amount of S or Mg that is ultimately incorporated in foraminiferal calcite, these processes do not explain the covariation between Mg∕Ca and S∕Ca values within specimens and between species. We observe that groups of foraminifera with different calcification pathways, e.g., hyaline versus porcelaneous species, show characteristic values for S∕Ca and Mg∕Ca, which might be linked to a different calcium and carbon uptake mechanism in porcelaneous and hyaline foraminifera. Whereas Mg incorporation might be controlled by Ca dilution at the site of calcification due to Ca pumping, S is linked to carbonate ion concentration via proton pumping. The fact that we observe a covariation of S and Mg within specimens and between species suggests that proton pumping and Ca pumping are intrinsically coupled across multiple scales.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2019
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  • 3
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    Copernicus GmbH ; 2018
    In:  Biogeosciences Vol. 15, No. 7 ( 2018-04-16), p. 2205-2218
    In: Biogeosciences, Copernicus GmbH, Vol. 15, No. 7 ( 2018-04-16), p. 2205-2218
    Abstract: Abstract. Accurate reconstructions of seawater salinity could provide valuable constraints for studying past ocean circulation, the hydrological cycle and sea level change. Controlled growth experiments and field studies have shown the potential of foraminiferal Na ∕ Ca as a direct salinity proxy. Incorporation of minor and trace elements in foraminiferal shell carbonate varies, however, greatly between species and hence extrapolating calibrations to other species needs validation by additional (culturing) studies. Salinity is also known to impact other foraminiferal carbonate-based proxies, such as Mg ∕ Ca for temperature and Sr ∕ Ca for sea water carbonate chemistry. Better constraints on the role of salinity on these proxies will therefore improve their reliability. Using a controlled growth experiment spanning a salinity range of 20 units and analysis of element composition on single chambers using laser ablation-Q-ICP-MS, we show here that Na ∕ Ca correlates positively with salinity in two benthic foraminiferal species (Ammonia tepida and Amphistegina lessonii). The Na ∕ Ca values differ between the two species, with an approximately 2-fold higher Na ∕ Ca in A. lessonii than in A. tepida, coinciding with an offset in their Mg content (∼ 35 mmol mol−2 versus ∼ 2.5 mmol mol−1 for A. lessonii and A. tepida, respectively). Despite the offset in average Na ∕ Ca values, the slopes of the Na ∕ Ca–salinity regressions are similar between these two species (0.077 versus 0.064 mmol mol−1 change per salinity unit). In addition, Mg ∕ Ca and Sr ∕ Ca are positively correlated with salinity in cultured A. tepida but show no correlation with salinity for A. lessonii. Electron microprobe mapping of incorporated Na and Mg of the cultured specimens shows that within chamber walls of A. lessonii, Na ∕ Ca and Mg ∕ Ca occur in elevated bands in close proximity to the primary organic lining. Between species, Mg banding is relatively similar, even though Mg content is 10 times lower and that variation within the chamber wall is much less pronounced in A. tepida. In addition, Na banding is much less prominent in this species than it is in A. lessonii. Inter-species differences in element banding reported here are hypothesized to be caused by differences in biomineralization controls responsible for element uptake.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
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  • 4
    In: Biogeosciences, Copernicus GmbH, Vol. 15, No. 20 ( 2018-10-15), p. 5991-6018
    Abstract: Abstract. 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 to 29.5 ∘C under constant salinity conditions. Foraminiferal Na∕Ca values positively correlate with seawater salinity (Na/CaT. sacculifer=0.97+0.115⋅salinity, R=0.97, p〈0.005). Temperature, on the other hand, exhibits no statistically significant relationship with Na∕Ca values, indicating salinity to be one of the dominant factors controlling Na incorporation. The culturing results are corroborated by measurements on T. sacculifer from Caribbean and Gulf of Guinea surface sediments, indicating no dissolution effect on Na∕Ca in foraminiferal calcite with increasing water depth up to 〉4 km. In conclusion, planktonic foraminiferal Na∕Ca can be applied as a potential proxy for reconstructing sea surface salinities, although species-specific calibrations might be necessary.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
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  • 5
    In: Biogeosciences, Copernicus GmbH, Vol. 20, No. 14 ( 2023-07-28), p. 3027-3052
    Abstract: Abstract. The chemical composition of mollusk shells is a useful tool in (paleo)climatology since it captures inter- and intra-annual variability in environmental conditions. Trace element and stable isotope analysis with improved sampling resolution now allows in situ determination of the composition of mollusk shell volumes precipitated at daily to sub-daily time intervals. Here, we discuss hourly resolved Mg / Ca, Mn / Ca, Sr / Ca, and Ba / Ca profiles measured by laser ablation inductively coupled plasma – mass spectrometry (ICP-MS) through shells of the photosymbiotic giant clams (Tridacna maxima, T. squamosa, and T. squamosina) and the non-photosymbiotic scallop Pecten maximus. Precise sclerochronological age models and spectral analysis allowed us to extract daily and tidal rhythms in the trace element composition of these shells. We find weak but statistically significant expressions of these periods and conclude that this cyclicity explains less than 10 % of the sub-annual variance in trace element profiles. Tidal and diurnal rhythms explain variability of, at most, 0.2 mmol mol−1 (∼ 10 % of mean value) in Mg / Ca and Sr / Ca, while ultradian Mn / Ca and Ba / Ca cyclicity has a median amplitude of less than 2 µmol mol−1 mol mol−1 (∼ 40 % and 80 % of the mean of Mn / Ca and Ba / Ca, respectively). Daily periodicity in Sr / Ca and Ba / Ca is stronger in Tridacna than in Pecten, with Pecten showing stronger tidal periodicity. One T. squamosa specimen which grew under a sunshade exhibits among the strongest diurnal cyclicity. Daily cycles in the trace element composition of giant clams are therefore unlikely to be driven by variations in direct insolation but rather reflect an inherent biological rhythmic process affecting element incorporation. Finally, the large amount of short-term trace element variability unexplained by tidal and daily rhythms highlights the dominance of aperiodic processes in mollusk physiology and/or environmental conditions over shell composition at the sub-daily scale. Future studies should aim to investigate whether this remaining variability in shell chemistry reliably records weather patterns or circulation changes in the animals' environment.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2023
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  • 6
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    Copernicus GmbH ; 2021
    In:  Biogeosciences Vol. 18, No. 2 ( 2021-01-18), p. 393-401
    In: Biogeosciences, Copernicus GmbH, Vol. 18, No. 2 ( 2021-01-18), p. 393-401
    Abstract: Abstract. Marine calcification is an important component of the global carbon cycle. The mechanism by which some organisms take up inorganic carbon for the production of their shells or skeletons, however, remains only partly known. Although foraminifera are responsible for a large part of the global calcium carbonate production, the process by which they concentrate inorganic carbon is debated. Some evidence suggests that seawater is taken up by vacuolization and participates relatively unaltered in the process of calcification, whereas other results suggest the involvement of transmembrane transport and the activity of enzymes like carbonic anhydrase. Here, we tested whether inorganic-carbon uptake relies on the activity of carbonic anhydrase using incubation experiments with the perforate, large benthic, symbiont-bearing foraminifer Amphistegina lessonii. Calcification rates, determined by the alkalinity anomaly method, showed that inhibition of carbonic anhydrase by acetazolamide (AZ) stopped most of the calcification process. Inhibition of photosynthesis either by 3-(3,4-Dichlorophenyl)-1,1-dimethylurea (DCMU) or by incubating the foraminifera in the dark also decreased calcification rates but to a lesser degree than with AZ. Results from this study show that carbonic anhydrase plays a key role in biomineralization of Amphistegina lessonii and indicates that calcification of those perforate, large benthic foraminifera might, to a certain extent, benefit from the extra dissolved inorganic carbon (DIC), which causes ocean acidification.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2021
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  • 7
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    Copernicus GmbH ; 2017
    In:  Biogeosciences Vol. 14, No. 3 ( 2017-02-02), p. 497-510
    In: Biogeosciences, Copernicus GmbH, Vol. 14, No. 3 ( 2017-02-02), p. 497-510
    Abstract: Abstract. In this study we analyzed the impact of seawater carbonate chemistry on the incorporation of elements in both hyaline and porcelaneous larger benthic foraminifera. We observed a higher incorporation of Zn and Ba when pCO2 increases from 350 to 1200 ppm. Modeling the activity of free ions as a function of pCO2 shows that speciation of some elements (like Zn and Ba) is mainly influenced by the formation of carbonate complexes in seawater. Hence, differences in foraminiferal uptake of these might be related primarily by the speciation of these elements in seawater. We investigated differences in trends in element incorporation between hyaline (perforate) and porcelaneous (imperforate) foraminifera in order to unravel processes involved in element uptake and subsequent foraminiferal calcification. In hyaline foraminifera we observed a correlation of element incorporation of different elements between species, reflected by a general higher incorporation of elements in species with higher Mg content. Between porcelaneous species, inter-element differences are much smaller. Besides these contrasting trends in element incorporation, however, similar trends are observed in element incorporation as a function of seawater carbonate chemistry in both hyaline and porcelaneous species. This suggests similar mechanisms responsible for the transportation of ions to the site of calcification for these groups of foraminifera, although the contribution of these processes might differ across species.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2017
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  • 8
    In: Biogeosciences, Copernicus GmbH, Vol. 14, No. 12 ( 2017-06-22), p. 3067-3082
    Abstract: Abstract. The Mn / Ca of calcium carbonate tests of living (rose-Bengal-stained) benthic foraminifera (Elphidium batialis, Uvigerina spp., Bolivina spissa, Nonionellina labradorica and Chilostomellina fimbriata) were determined in relation to pore water manganese (Mn) concentrations for the first time along a bottom water oxygen gradient across the continental slope along the NE Japan margin (western Pacific). The local bottom water oxygen (BWO) gradient differs from previous field study sites focusing on foraminiferal Mn / Ca and redox chemistry, therefore allowing further resolution of previously observed trends. The Mn / Ca ratios were analysed using laser ablation inductively coupled plasma-mass spectrometer (ICP-MS), allowing single-chamber determination of Mn / Ca. The incorporation of Mn into the carbonate tests reflects environmental conditions and is not influenced by ontogeny. The inter-species variability in Mn / Ca reflected foraminiferal in-sediment habitat preferences and associated pore water chemistry but also showed large interspecific differences in Mn partitioning. At each station, Mn / Ca ratios were always lower in the shallow infaunal E. batialis, occupying relatively oxygenated sediments, compared to intermediate infaunal species, Uvigerina spp. and B. spissa, which were typically found at greater depth, under more reducing conditions. The highest Mn / Ca was always recorded by the deep infaunal species N. labradorica and C. fimbriata. Our results suggest that although partitioning differs, Mn / Ca ratios in the intermediate infaunal taxa are promising tools for palaeoceanographic reconstructions as their microhabitat exposes them to higher variability in pore water Mn, thereby making them relatively sensitive recorders of redox conditions and/or bottom water oxygenation.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2017
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  • 9
    In: Biogeosciences, Copernicus GmbH, Vol. 17, No. 9 ( 2020-05-12), p. 2499-2519
    Abstract: Abstract. Hydrothermal vent fields found at mid-ocean ridges emit hydrothermal fluids that disperse as neutrally buoyant plumes. From these fluids seafloor massive sulfides (SMS) deposits are formed, which are being explored as possible new mining sites for (trace) metals and rare earth elements (REEs). It has been suggested that during mining activities large amounts of suspended matter will appear in the water column due to excavation processes and discharge of mining waste from the surface vessel. Understanding how hydrothermal plumes can be characterised by means of geochemistry and microbiology as they spread away from their source and how they affect their surrounding environment may help in characterising the behaviour of the dilute distal part of chemically enriched mining plumes. This study on the extensive Rainbow hydrothermal plume, observed up to 25 km downstream from the vent site, enabled us to investigate how microbial communities and (trace) metal composition change in a natural plume with distance. The (trace) metal and REE content of suspended particulate matter (SPM) was determined using sector field inductively coupled plasma mass spectrometry (SF-ICP-MS) with high resolution (HR), and the microbial communities of the neutrally buoyant plume, above-plume, below-plume, and near-bottom water and sediment were characterised by using 16S rRNA amplicon sequencing methods. Both vertically in the water column and horizontally along the neutrally buoyant plume, geochemical and biological changes were evident, as the neutrally buoyant plume stood out by its enrichments in (trace) metals and REEs, as, for example, Fe, Cu, V, Mn and REEs were enriched by factors of up to ∼80, ∼90, ∼52, ∼2.5 and ∼40, respectively, compared to above-plume water samples taken at 1000 m water depth. The concentrations of these elements changed as the plume aged, shown by the decrease in element ∕ Fe molar ratios of chalcophile elements (Cu, Co, Zn), indicative of rapid removal from the hydrothermal plume or removal from the solid phase. Conversely, increasing REE ∕ Fe molar ratios imply uptake of REEs from the ambient seawater onto Fe-oxyhydroxides. This was also reflected in the background pelagic system, as Epsilonproteobacteria started to dominate and univariate microbial biodiversity declined with distance away from the Rainbow hydrothermal vent field. The Rainbow hydrothermal plume provides a geochemically enriched natural environment, which is a heterogeneous, dynamic habitat that is conducive to ecological changes in a short time span. This study of a hydrothermal plume provides a baseline study to characterise the natural plume before the interference of deep-sea mining.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2020
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  • 10
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    Copernicus GmbH ; 2017
    In:  Biogeosciences Vol. 14, No. 14 ( 2017-07-19), p. 3387-3400
    In: Biogeosciences, Copernicus GmbH, Vol. 14, No. 14 ( 2017-07-19), p. 3387-3400
    Abstract: Abstract. Barium (Ba) incorporated in the calcite of many foraminiferal species is proportional to the concentration of Ba in seawater. Since the open ocean concentration of Ba closely follows seawater alkalinity, foraminiferal Ba ∕ Ca can be used to reconstruct the latter. Alternatively, Ba ∕ Ca from foraminiferal shells can also be used to reconstruct salinity in coastal settings in which seawater Ba concentration corresponds to salinity as rivers contain much more Ba than seawater. Incorporation of a number of minor and trace elements is known to vary (greatly) between foraminiferal species, and application of element ∕ Ca ratios thus requires the use of species-specific calibrations. Here we show that calcite Ba ∕ Ca correlates positively and linearly with seawater Ba ∕ Ca in cultured specimens of two species of benthic foraminifera: Heterostegina depressa and Amphistegina lessonii. The slopes of the regression, however, vary two- to threefold between these two species (0.33 and 0.78, respectively). This difference in Ba partitioning resembles the difference in partitioning of other elements (Mg, Sr, B, Li and Na) in these foraminiferal taxa. A general trend across element partitioning for different species is described, which may help develop new applications of trace elements in foraminiferal calcite in reconstructing past seawater chemistry.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2017
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