GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Book
    Book
    Amsterdam [u.a.] : Elsevier
    Type of Medium: Book
    Pages: VI, 194 S , Ill., graph. Darst
    Series Statement: Marine chemistry 120.2010,1/4
    Language: English
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2020-02-06
    Description: The geological calcium cycle is linked to the geological carbon cycle through the weathering and burial of carbonate rocks. As a result, calcium (Ca) isotope ratios (44Ca/40Ca, expressed as δ44/40Ca) can help to constrain ancient carbon cycle dynamics if Ca cycle behavior can be reconstructed. However, the δ44/40Ca of carbonate rocks is influenced not only by the δ44/40Ca of seawater but also by diagenetic processes and fractionation associated with carbonate precipitation. In this study, we investigate the dominant controls on carbonate δ44/40Ca in Upper Permian to Middle Triassic limestones (ca. 253 to 244 Ma) from south China and Turkey. This time interval is ideal for assessing controls on Ca isotope ratios in carbonate rocks because fluctuations in seawater δ44/40Ca may be expected based on several large carbon isotope (δ13C) excursions ranging from − 2 to + 8‰. Parallel negative δ13C and δ44/40Ca excursions were previously identified across the end-Permian extinction horizon. Here, we find a second negative excursion in δ44/40Ca of ~ 0.2‰ within Lower Triassic strata in both south China and Turkey; however, this excursion is not synchronous between regions and thus cannot be interpreted to reflect secular change in the δ44/40Ca of global seawater. Additionally, δ44/40Ca values from Turkey are consistently 0.3‰ lower than contemporaneous samples from south China, providing further support for local or regional influences. By measuring δ44/40Ca and Sr concentrations ([Sr]) in two stratigraphic sections located at opposite margins of the Paleo-Tethys Ocean, we can determine whether the data represent global conditions (e.g., secular variations in the δ44/40Ca of seawater) versus local controls (e.g., original mineralogy or diagenetic alteration). The [Sr] and δ44/40Ca data from this study are best described statistically by a log-linear correlation that also exists in many previously published datasets of various geological ages. Using a model of early marine diagenetic water-rock interaction, we illustrate that this general correlation can be explained by the chemical evolution of bulk carbonate sediment samples with different initial mineralogical compositions that subsequently underwent recrystallization. Although early diagenetic resetting and carbonate mineralogy strongly influence the carbonate δ44/40Ca values, the relationship between [Sr] and δ44/40Ca holds potential for reconstructing first-order secular changes in seawater δ44/40Ca composition.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2021-02-08
    Description: Coccoliths comprise a major fraction of the global carbonate sink. Therefore, changes in coccolithophores' Ca isotopic fractionation could affect seawater Ca isotopic composition, affecting interpretations of the global Ca cycle and related changes in seawater chemistry and climate. Despite this, a quantitative interpretation of coccolith Ca isotopic fractionation and a clear understanding of the mechanisms driving it are not yet available. Here, we address this gap in knowledge by developing a simple model (CaSri–Co) to track coccolith Ca isotopic fractionation during cellular Ca uptake and allocation to calcification. We then apply it to published and new δ44/40Ca and Sr/Ca data of cultured coccolithophores of the species Emiliania huxleyi and Gephyrocapsa oceanica. We identify changes in calcification rates, Ca retention efficiency and solvation–desolvation rates as major drivers of the Ca isotopic fractionation and Sr/Ca variations observed in cultures. Higher calcification rates, higher Ca retention efficiencies and lower solvation–desolvation rates increase both coccolith Ca isotopic fractionation and Sr/Ca. Coccolith Ca isotopic fractionation is most sensitive to changes in solvation–desolvation rates. Changes in Ca retention efficiency may be a major driver of coccolith Sr/Ca variations in cultures. We suggest that substantial changes in the water structure strength caused by past changes in temperature could have induced significant changes in coccolithophores' Ca isotopic fractionation, potentially having some influence on seawater Ca isotopic composition. We also suggest a potential effect on Ca isotopic fractionation via modification of the solvation environment through cellular exudates, a hypothesis that remains to be tested.
    Type: Article , PeerReviewed
    Format: text
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2017-12-19
    Description: Highlights • δ44Ca was measured in bulk carbonate and barite at two sites over the PETM. • Diagenetic effects on δ44Ca are observed associated with ocean acidification. • Multiple sites and proxy archives necessary to reconstruct the past accurately. Abstract Carbonates are used extensively to reconstruct paleoclimate and paleoceanographic conditions over geologic time scales. However, these archives are susceptible to diagenetic alteration via dissolution, recrystallization and secondary precipitation, particularly during ocean acidification events when intense dissolution can occur. Despite the possible effects of diagenesis on proxy fidelity, the impacts of diagenesis on the calcium isotopic composition (δ44Ca) of carbonates are unclear. To shed light on this issue, bulk carbonate δ44Ca was measured at high resolution in two Pacific deep sea sediment cores (ODP Sites 1212 and 1221) with considerably different dissolution histories over the Paleocene–Eocene Thermal Maximum (PETM, ∼55 Ma∼55 Ma). The δ44Ca of marine barite was also measured at the deeper Site 1221, which experienced severe carbonate dissolution during the PETM. Large variations (∼0.8‰∼0.8‰) in bulk carbonate δ44Ca occur in the deeper of the two sites at depths corresponding to the peak carbon isotope excursion, which correlate with a large drop in carbonate weight percent. Such an effect is not observed in either the 1221 barite record or the bulk carbonate record at the shallower Site 1212, which is also less affected by dissolution. We contend that ocean chemical changes associated with abrupt and massive carbon release into the ocean–atmosphere system and subsequent ocean acidification at the PETM affected the bulk carbonate δ44Ca record via diagenesis in the sedimentary column. Such effects are considerable, and need to be taken into account when interpreting Ca isotope data and, potentially, other geochemical proxies over extreme climatic events that drive sediment dissolution.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Publication Date: 2023-02-08
    Description: Boron isotope (δ11B) analysis using bulk foraminifera samples is a widely used method to reconstruct paleo sea water pH conditions. Although, these analyses exhibit high analytical precision, short term information is lost due to the pooling of tests with distinct and diverse boron isotope signatures resulting in average values for the time interval encompassed in the sample. Here we present and assess the analysis of δ11B of individual foraminifera by means of Laser Ablation Multi-Collector Inductively Coupled Plasma Mass Spectrometry (LA-MC-ICP-MS) to obtain seasonal variability patterns and to test the limits of precision of LA-MC-ICP-MS on the planktonic foraminifera Orbulina universa. The results show that relative seasonal differences (of ∼11 ‰) can be captured from either uncleaned or cleaned individual O. universa tests with an average precision of ±2.9 ‰ (2 SE). The δ11B variability among foraminifera representing the same season is on average 7.4 ‰ (2 SD) irrespective of cleaning state. With our approach, analyses on oxidatively cleaned O. universa do not require the use of a matrix matched standard to obtain B isotope values in the range of those expected for solution multi-specimen analyses from determining local pH. Our results are useful for considering the potential spread caused by foraminifera vital effects and for obtaining information of seasonal ranges of pH and possible bias related to seasonality hidden within conventional solution based δ11B analyses.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Publication Date: 2022-01-31
    Description: Atmospheric deposition can be an important source of nutrients and trace metals to oligotrophic alpine lakes, affecting their biogeochemistry. We measured trace metal concentrations and lead (Pb) isotope ratios in lake water, river water, ground water, and aerosol total suspended particles (TSP), as well as nutrient (NO 3 − , NH 4 + , PO 4 3− ) concentrations in TSP in the Tahoe Basin. The contribution of TSP deposition to the lake trace metal budget was assessed. Our results show seasonality in TSP and associated trace metal concentrations with higher concentrations during Oct – April. However, trace metal solubilities are higher during May – Sept, resulting in a higher contribution of soluble trace metals to the lake water. The source of most of the trace metals in TSP in the Lake Tahoe Basin is mineral dust; however, Zn, Cu, and Cd also have an anthropogenic origin. Among major nutrients, NO 3 − concentrations are slightly higher during Oct – April, while NH 4 + and soluble reactive phosphorus (SRP) are higher during May – Sept. The distributions of trace metal concentrations and Pb isotopic ratios are homogenous throughout the lake water column, suggesting that the residence time of the trace metals in the lake is longer than the lake water mixing time. The contribution of atmospheric TSP deposition to the upper 20 m of lake water trace metal inventory is low, ranging from 0.03% for V to 5.7% for Mn. A triple-isotopes plot of Pb indicates that riverine and groundwater inputs are the major Pb sources, but aerosols still contribute some Pb to the lake. This article is part of a special issue entitled: Conway GEOTRACES - edited by Tim M. Conway, Tristan Horner, Yves Plancherel, and Aridane G. González.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    Publication Date: 2021-11-05
    Description: Highlights • Hydrologic, biologic processes play key roles in barite formation and geochemistry. • Sulfur and oxygen isotopes distinguish sulfate sources and (bio)chemical processes. • Radiogenic Sr identifies fluid sources, stable Sr isotopic signatures are not unique. • Marine pelagic barite stable Sr isotopes have consistent offset from seawater. Abstract Barite (BaSO4) is a highly stable and widely-distributed mineral found in magmatic, metamorphic, and sedimentary rocks of all ages, as well as in soils, aerosol dust, and extraterrestrial material. Barite can form in a variety of settings in the oceans (hydrothermal deposits, cold seeps, water column, or within sediments) and on the continents (soils, sulfidic springs and in the subsurface) when (1) two fluids mix – one containing barium and another containing sulfate, (2) sulfur is oxidized forming sulfate in a barium containing solution, or (3) barium or sulfate is concentrated in microenvironments where either sulfate or barium are already present. Hydrologic and biologic processes can therefore play key roles in the formation of barite and affect its geochemical composition. Characteristics of barite from various modern settings are identified here to serve as analogs for ancient systems, summarizing previous work and adding new details from the pelagic marine, hydrothermal, cold seep and continental setting. Radiogenic strontium in barite clearly identifies the source(s) of fluid forming barite with the most radiogenic values measured in continental sulfidic spring settings associated with a deep fluid component that interacts with ancient crustal rocks. Sulfur and oxygen isotopes can distinguish between sources of sulfate and identify settings where the influence of (bio)chemical processes such as sulfate reduction is prominent. There are no unique stable strontium isotopic signatures for barite formed in any of the settings investigated here, but Holocene coretop marine pelagic barite appears to have a constant offset from seawater of approximately −0.53‰ in coretop samples in contrast to the wide range of values in barite precipitated in other settings. Stable strontium mass dependent fractionation could be useful in understanding post-depositional and diagenetic processes such as authigenic precipitation and recrystallization.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 2024-02-07
    Description: Highlights • Hydrography and convection reconstructed in the Nordic Seas during MIS 11. • Active convection in the Nordic Seas occurred during prolonged freshwater input. • Freshwater input does not always impede convection on interglacial timescales. • Onset of polar convection may have helped to sustain interglacial conditions. Abstract The Atlantic meridional overturning circulation (AMOC) is a critical element of Earth's climate system and it is currently weakening. While this weakening is frequently explained by freshwater-driven disruptions to deep-water formation, uncertainties about the impacts of prolonged freshening limit our capacity to predict its future state. For example, during the warm and unusually long marine isotope stage (MIS) 11 interglacial, ∼424 to 374 ka, several lines of evidence suggest that a strong AMOC persisted concomitant with fresher-than-present conditions in the Nordic Seas, challenging our current understanding of deep-water formation. Here, we present new foraminifer-bound nitrogen isotope data along with multiple additional geochemical reconstructions of upper-ocean hydrography in the Nordic Seas during this anomalous interval. Our data suggest that a weak summer stratification was driven by the prolonged upper-ocean accumulation of freshwater beginning at the onset of the climatic optimum, ∼410 to 407 ka, which could have helped precondition the region for deep-water formation. A box model constrained by paleo-proxy data additionally suggests that the density gradient between the subpolar North Atlantic and Nordic Seas was favorable for the onset of deep-water formation in the Nordic Seas during the climatic optimum. It is thus likely that the Nordic Seas became a locus of deep-water formation around this time. Enhanced northern-hemisphere heating driven by deep-water formation in the Nordic Seas may have been important for delaying glacial conditions, thereby driving the extended warming characteristic of MIS 11. Such findings may also be relevant for near-future changes under a relatively fresher high-latitude North Atlantic.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    Publication Date: 2024-02-07
    Description: Highlights • Dual geochemical approach using δ11B and B/Ca to evaluate coral calcifying fluids from West Maui, Hawai'i. • NMR analysis confirms boron is present as borate with no evidence of boric acid inclusion. • Increased pH up-regulation in corals exposed to high nutrient / low pH submarine groundwater discharge. • Calcifying fluid aragonite saturate state 9 to 10 times higher than ambient seawater. • Up-regulation as an internal coping mechanism to combat multiple stressors from land-based sources of pollution. Coral reefs and their ecosystems are threatened by both global stressors, including increasing sea-surface temperatures and ocean acidification (OA), and local stressors such as land-based sources of pollution that can magnify the effects of OA. Corals can physiologically control the chemistry of their internal calcifying fluids (CF) and can thereby regulate their calcification process. Specifically, increasing aragonite saturation state in the CF (ΩCF) may allow corals to calcify even under external low saturation conditions. Questions remain regarding the physiological processes that govern the CF chemistry and how they change in response to multiple stressors. To address this knowledge gap, the boron systematics (δ11B and B/Ca) were analyzed in tropical corals, Porites lobata, collected at submarine groundwater seeps impacted by the release of treated wastewater in west Maui, Hawai'i, to document the interactions between high nutrient / low pH seep water on CF carbonate chemistry. Results show substantial up-regulation of pH and dissolved inorganic carbon (DIC) with respect to seawater in P. lobata corals collected from within the wastewater impacted area at Kahekili Beach Park compared to the control site at Olowalu Beach. The ΩCF was 9 to 10 times higher than ambient seawater Ω, and 13 to 26% higher than in corals from the control site and from previously observed in tropical Porites spp. corals. Such elevated up-regulation suggests that corals exposed to nutrient-enriched, low pH effluent sustain CF supersaturated with respect to aragonite, possibly as an internal coping mechanism to combat multiple stressors from land-based sources of pollution. This elevated up-regulation has implications to coral vulnerability to future climate- and ocean-change scenarios.
    Type: Article , PeerReviewed
    Format: text
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 10
    Publication Date: 2011-07-01
    Description: During the Eocene-Oligocene transition (EOT, ca. 34 Ma), Earth's climate cooled significantly from a greenhouse to an icehouse climate, while the calcite (CaCO3) compensation depth (CCD) in the Pacific Ocean increased rapidly. Fluctuations in the CCD could result from various processes that create an imbalance between calcium (Ca) sources to, and sinks from, the ocean (e.g., weathering and CaCO3 deposition), with different effects on the isotopic composition of dissolved Ca in the oceans due to differences in the Ca isotopic composition of various inputs and outputs. We used Ca isotope ratios ({delta}44/40Ca) of coeval pelagic marine barite and bulk carbonate to evaluate changes in the marine Ca cycle across the EOT. We show that the permanent deepening of the CCD was not accompanied by a pronounced change in seawater {delta}44/40Ca, whereas time intervals in the Neogene with smaller carbonate depositional changes are characterized by seawater {delta}44/40Ca shifts. This suggests that the response of seawater {delta}44/40Ca to changes in weathering fluxes and to imbalances in the oceanic alkalinity budget depends on the chemical composition of seawater. A minor and transient fluctuation in the Ca isotope ratio of bulk carbonate may reflect a change in isotopic fractionation associated with CaCO3 precipitation from seawater due to a combination of factors, including changes in temperature and/or in the assemblages of calcifying organisms.
    Print ISSN: 0091-7613
    Electronic ISSN: 1943-2682
    Topics: Geosciences
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...