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  • 1
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    Authigenic Formation of Clay Minerals in the Abyssal North Pacific (2022)
    Details
    Publication Date: 2023-07-19
    Description: Present estimates of the biogeochemical cycles of calcium, strontium, and potassium in the ocean reveal large imbalances between known input and output fluxes. Using pore fluid, incubation, and solid sediment data from North Pacific multi‐corer cores we show that, contrary to the common paradigm, the top centimeters of abyssal sediments can be an active site of authigenic precipitation of clay minerals. In this region, clay authigenesis is the dominant sink for potassium and strontium and consumes nearly all calcium released from benthic dissolution of calcium carbonates. These observations support the idea that clay authigenesis occurring over broad regions of the world ocean may be a major buffer for ocean chemistry on the time scale of the ocean overturning circulation, and key to the long‐term stability of Earth's climate.
    Description: Key Points: North Pacific red clay sediments are a sink for marine calcium, strontium, and potassium. Authigenic formation of clay minerals is prevalent in pelagic sediments throughout the North Pacific. The main mechanism for clay formation is recrystallization of aluminosilicates, neoformation can occur in biogenic silica rich sediments.
    Description: EC H2020 PRIORITY “Excellent science” H2020 European Research Council http://dx.doi.org/10.13039/100010663
    Description: Blavatnik Family Foundation http://dx.doi.org/10.13039/100011643
    Description: Isaac Newton Trust http://dx.doi.org/10.13039/501100004815
    Description: Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659
    Description: National Science Foundation http://dx.doi.org/10.13039/100000001
    Description: https://doi.pangaea.de/10.1594/PANGAEA.946881
    Keywords: ddc:549 ; reverse weathering ; clay authigenesis ; calcium ; potassium ; porewater ; strontium
    Language: English
    Type: doc-type:article
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    CITATION GEO-LEO
  • 2
    Electronic Resource
    Electronic Resource
    Variability of the North Atlantic thermohaline circulation during the last interglacial period (1997)
    [s.l.] : Macmillan Magazines Ltd.
    Nature 390 (1997), S. 154-156 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Studies of natural climate variability are essential for evaluating its future evolution. Greenland ice cores suggest that the modern warm period (the Holocene) has been relatively stable for the past 9,000 years. Much less is known about other warm interglacial periods, which comprise less ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/36540
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    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Millennial-scale trends in west Pacific warm pool hydrology since the Last Glacial Maximum (2007)
    [s.l.] : Nature Publishing Group
    Nature 449 (2007), S. 452-455 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Models and palaeoclimate data suggest that the tropical Pacific climate system plays a key part in the mechanisms underlying orbital-scale and abrupt climate change. Atmospheric convection over the western tropical Pacific is a major source of heat and moisture to extratropical regions, and ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/nature06164
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    Paper (German National Licenses)
    Fulltext
  • 4
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    Glacial weathering, sulfide oxidation, and global carbon cycle feedbacks (2017)
    National Academy of Sciences
    In:  Proceedings of the National Academy of Sciences of the United States of America (PNAS), 114 (33). pp. 8716-8721.
    Details
    Publication Date: 2020-02-06
    Description: Connections between glaciation, chemical weathering, and the global carbon cycle could steer the evolution of global climate over geologic time, but even the directionality of feedbacks in this system remain to be resolved. Here, we assemble a compilation of hydrochemical data from glacierized catchments, use this data to evaluate the dominant chemical reactions associated with glacial weathering, and explore the implications for long-term geochemical cycles. Weathering yields from catchments in our compilation are higher than the global average, which results, in part, from higher runoff in glaciated catchments. Our analysis supports the theory that glacial weathering is characterized predominantly by weathering of trace sulfide and carbonate minerals. To evaluate the effects of glacial weathering on atmospheric pCO2, we use a solute mixing model to predict the ratio of alkalinity to dissolved inorganic carbon (DIC) generated by weathering reactions. Compared with nonglacial weathering, glacial weathering is more likely to yield alkalinity/DIC ratios less than 1, suggesting that enhanced sulfide oxidation as a result of glaciation may act as a source of CO2 to the atmosphere. Back-of-the-envelope calculations indicate that oxidative fluxes could change ocean–atmosphere CO2 equilibrium by 25 ppm or more over 10 ky. Over longer timescales, CO2 release could act as a negative feedback, limiting progress of glaciation, dependent on lithology and the concentration of atmospheric O2. Future work on glaciation–weathering–carbon cycle feedbacks should consider weathering of trace sulfide minerals in addition to silicate minerals.
    Type: Article , PeerReviewed
    Format: text
    DOI: 10.1073/pnas.1702953114
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 5
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    Synchronous volcanic eruptions and abrupt climate change ∼17.7 ka plausibly linked by stratospheric ozone depletion (2017)
    National Academy of Sciences
    In:  PNAS Proceedings of the National Academy of Sciences of the United States of America, 114 (38). pp. 10035-10040.
    Details
    Publication Date: 2020-02-06
    Description: Significance: Cold and dry glacial-state climate conditions persisted in the Southern Hemisphere until approximately 17.7 ka, when paleoclimate records show a largely unexplained sharp, nearly synchronous acceleration in deglaciation. Detailed measurements in Antarctic ice cores document exactly at that time a unique, ∼192-y series of massive halogen-rich volcanic eruptions geochemically attributed to Mount Takahe in West Antarctica. Rather than a coincidence, we postulate that halogen-catalyzed stratospheric ozone depletion over Antarctica triggered large-scale atmospheric circulation and hydroclimate changes similar to the modern Antarctic ozone hole, explaining the synchronicity and abruptness of accelerated Southern Hemisphere deglaciation. Abstract: Glacial-state greenhouse gas concentrations and Southern Hemisphere climate conditions persisted until ∼17.7 ka, when a nearly synchronous acceleration in deglaciation was recorded in paleoclimate proxies in large parts of the Southern Hemisphere, with many changes ascribed to a sudden poleward shift in the Southern Hemisphere westerlies and subsequent climate impacts. We used high-resolution chemical measurements in the West Antarctic Ice Sheet Divide, Byrd, and other ice cores to document a unique, ∼192-y series of halogen-rich volcanic eruptions exactly at the start of accelerated deglaciation, with tephra identifying the nearby Mount Takahe volcano as the source. Extensive fallout from these massive eruptions has been found 〉2,800 km from Mount Takahe. Sulfur isotope anomalies and marked decreases in ice core bromine consistent with increased surface UV radiation indicate that the eruptions led to stratospheric ozone depletion. Rather than a highly improbable coincidence, circulation and climate changes extending from the Antarctic Peninsula to the subtropics—similar to those associated with modern stratospheric ozone depletion over Antarctica—plausibly link the Mount Takahe eruptions to the onset of accelerated Southern Hemisphere deglaciation ∼17.7 ka.
    Type: Article , PeerReviewed
    Format: text
    DOI: 10.1073/pnas.1705595114
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 6
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    Carbonic anhydrase, coral calcification and a new model of stable isotope vital effects (2018)
    Elsevier
    In:  Geochimica et Cosmochimica Acta, 236 . pp. 179-197.
    Details
    Publication Date: 2021-02-08
    Description: The stable isotope compositions of biogenic carbonates have been used for paleoceanographic and paleoclimatic reconstructions for decades, and produced some of the most iconic records in the field. However, we still lack a fully mechanistic understanding of the stable isotope proxies, especially the biological overprint on the environmental signals termed “vital effects”. A ubiquitous feature of stable isotope vital effects in marine calcifying organisms is a strong correlation between δ18O and δ13C in a range of values that are depleted from inorganic calcite/aragonite. Two mechanisms have been proposed to explain this correlation, one based on kinetic isotope effects during CO2(aq)-HCO3− inter-conversion, the other based on equilibrium isotope exchange during pH dependent speciation of the dissolved inorganic carbon (DIC) pool. Neither mechanism explains all the stable isotope features observed in biogenic carbonates. Here we present a fully kinetic model of biomineralization and its isotope effects using deep-sea corals as a test organism. A key component of our model is the consideration of the enzyme carbonic anhydrase in catalyzing the CO2(aq)-HCO3− inter-conversion reactions in the extracellular calcifying fluid (ECF). We find that the amount of carbonic anhydrase not only modulates the carbonate chemistry of the calcifying fluid, but also helps explain the slope of the δ18O-δ13C correlation. Differences in CA activity in the biomineralization process can possibly explain the observed range of δ18O-δ13C slopes in different calcifying organisms. A mechanistic understanding of stable isotope vital effects with numerical models can help us develop better paleoceanographic tracers.
    Type: Article , PeerReviewed
    Format: text
    DOI: 10.1016/j.gca.2018.02.032
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 7
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    Shallow Calcium Carbonate Cycling in the North Pacific Ocean (2022)
    AGU (American Geophysical Union) | Wiley
    Details
    Publication Date: 2024-02-07
    Description: Key Points: - High resolution carbonate chemistry, δ13C-DIC, and particle flux measurements in the NE Pacific sheds light on the upper oceancalcium carbonate and alkalinity cycles. - Based on this sampling campaign, there isevidence for substantial CaCO3 dissolution in the mesopelagic zone above the saturation horizon. - Dissolution experiments, observations, and modeling suggest that shallow CaCO3 dissolutionis coupled to the consumption of organic carbon, through a combination of zooplankton grazing and oxic respiration within particle microenvironments. The cycling of biologically produced calcium carbonate (CaCO3) in the ocean is a fundamental component of the global carbon cycle. Here, we present experimental determinations of in situcoccolith and foraminiferal calcite dissolution rates.We combine these rates with solid phase fluxes,dissolved tracers, and historical data to constrain the alkalinity cycle in the shallow North Pacific Ocean.The in situ dissolution rates of coccolithophores demonstrate a nonlinear dependence on saturation state. Dissolution ratesof all three major calcifying groups (coccoliths, foraminifera, and aragonitic pteropods)aretoo slow to explainthe patternsofboth CaCO3sinking fluxand alkalinity regenerationin the NorthPacific.Usinga combination of dissolved and solid-phase tracers, we document a significant dissolution signal in seawater supersaturated for calcite. Driving CaCO3dissolutionwith acombination of ambient saturation state and oxygen consumption simultaneously explainssolid-phase CaCO3flux profiles and patterns of alkalinity regeneration across the entire N. Pacific basin. Wedo not need to invokethe presence ofcarbonate phases with higher solubilities.Instead, biomineralization and metabolic processesintimately associatethe acid (CO2) and the base (CaCO3) in the same particles,driving the coupled shallow remineralization of organic carbonand CaCO3.The linkage of these processes likely occurs through a combination of dissolution due to zooplankton grazing and microbial aerobic respiration withindegrading particle aggregates.The coupling of these cyclesacts as a major filter on the export of both organic and inorganic carbon to the deep ocean.
    Type: Article , PeerReviewed
    Format: other
    Format: text
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 8
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    Trace Element Geochemistry in North Pacific Red Clay Sediment Porewaters and Implications for Water‐Column Studies (2023)
    AGU (American Geophysical Union) | Wiley
    Details
    Publication Date: 2024-02-07
    Description: Geochemical analyses of trace elements in the ocean water column have suggested that pelagic clay‐rich sediments are a major source of various elements to bottom‐waters. However, corresponding high‐quality measurements of trace element concentrations in porewaters of pelagic clay‐rich sediments are scarce, making it difficult to evaluate the contributions from benthic processes to global oceanic cycles of trace elements. To bridge this gap, we analyzed porewater and bulk sediment concentrations of vanadium, chromium, cobalt, nickel, copper, arsenic, molybdenum, barium and uranium, as well as concentrations of the major oxidants nitrate, manganese, iron, and sulfate in the top 30 cm of cores collected along a transect from Hawaii to Alaska. The data show large increases in porewater concentrations of vanadium, manganese, cobalt, nickel, copper, and arsenic within the top cm of the sediment, consistent with the release of these elements from remineralized organic matter. The sediments are a sink for sulfate, uranium, and molybdenum, even though conditions within the sampled top 30 cm remain aerobic. Porewater chromium concentrations generally increase with depth due to release from sediment particles. Extrapolated to the global aerial extent of pelagic clay sediment, the benthic fluxes in mol yr −1 are Ba 3.9 ± 3.6 × 10 9 , Mn 3.4 ± 3.5 × 10 8 , Co 2.6 ± 1.3 × 10 7 , Ni 9.6 ± 8.6 × 10 8 , Cu 4.6 ± 2.4 × 10 9 , Cr 1.7 ± 1.1 × 10 8 , As 6.1 ± 7.0 × 10 8 , V 6.0 ± 2.5 × 10 9 . With the exception of vanadium, calculated fluxes across the sediment–water interface are consistent with the variability in bottom‐water concentrations and ocean residence time of the studied elements.
    Type: Article , PeerReviewed
    Format: text
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 9
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    On calcium-to-alkalinity anomalies in the North Pacific, Red Sea, Indian Ocean and Southern Ocean (2021)
    Elsevier
    Details
    Publication Date: 2024-02-07
    Description: An important factor for predicting the effect of increased CO2 on future acidification of the ocean is a proper understanding of the interactions controlling production and dissolution of calcium carbonate minerals (CaCO3). The production and dissolution of CaCO3 in the ocean can be assessed over large spatial scales by measuring seawater calcium concentrations and total alkalinity (AT), yet past studies suggest that there could be large discrepancies between calcium and AT-based balances of the CaCO3 cycle in the North Pacific and Indian Oceans. Here, we analyse water column samples collected along transects in the North Pacific, Southern Ocean, tropical Indian Ocean and Red Sea for their concentrations of calcium, nutrients, and AT. We find that there is an excess calcium over AT anomaly in the top 1000 m of the tropical Indian Ocean water-column. The source of this anomaly is the dissolution of subsurface gypsum deposits in the Red Sea. We find no evidence for calcium-over-AT anomalies in the North Pacific, in contrast to previous studies. Our results show that, in most cases, calcium and AT data agree well and can be used to reconstruct the marine CaCO3 cycle.
    Type: Article , PeerReviewed
    Format: text
    Format: text
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    OceanRep: Article in a Scientific Journal - peer-reviewed
  • 10
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    Authigenic formation of clay minerals in the abyssal North Pacific (2022)
    AGU (American Geophysical Union) | Wiley
    Details
    Publication Date: 2024-02-07
    Description: Present estimates of the biogeochemical cycles of calcium, strontium and potassium in the ocean reveal large imbalances between known input and output fluxes. Using pore fluid, incubation and solid sediment data from North Pacific multi-corer cores we show that, contrary to the common paradigm, the top centimetres of abyssal sediments can be an active site of authigenic precipitation of clay minerals. In this region, clay authigenesis is the dominant sink for potassium and strontium and consumes nearly all calcium released from benthic dissolution of calcium carbonates. These observations support the idea that clay authigenesis occurring over broad regions of the world ocean may be a major buffer for ocean chemistry on the time scale of the ocean overturning circulation, and key to the long-term stability of Earth’s climate. Key Points North Pacific red clay sediments are a sink for marine calcium, strontium and potassium Authigenic formation of clay minerals is prevalent in pelagic sediments throughout the North Pacific The main mechanism for clay formation is recrystallisation of aluminosilicates, neoformation can occur in biogenic silica rich sediments
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
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    OceanRep: Article in a Scientific Journal - peer-reviewed
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