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  • 1
    Publication Date: 2019-09-23
    Description: In order to evaluate the influence of diagenetic and post-sampling processes on the stable oxygen and carbon isotope compositions of biogenic carbonates, we conducted a multiproxy study of organic-rich sediments from the eastern Pacific oxygen minimum zone. Core MD02-2520, which was retrieved from the Gulf of Tehuantepec (Mexico), has seasonal laminations and covers the last 40 kyr. Together with the presence of gypsum crystals and inorganic calcite aggregates, the occurrence of large excursions in the stable oxygen and carbon isotope records of both planktonic and benthic foraminifera (as large as +3‰ in d18O and -5‰ in d13C) point to significant secondary transformations. Storage-related gypsum precipitation was ruled out since it implies sulfide reoxidation by oxygen that triggers biogenic calcite dissolution, which proved to be of minor importance here. Instead, precipitation of authigenic calcite during early diagenesis appears to be the most likely process responsible for the observed isotopic excursions. The d13C composition for inorganic calcite aggregates (-5 to -7‰) suggests a major contribution from anaerobic oxidation of organic matter. The d34S composition for gypsum crystals (-10 to +15‰) suggests a major contribution from anaerobic reoxidation of authigenic sulfides, potentially involving reactions with metal oxides and sulfur disproportionation. A minor part of the gypsum might possibly have formed as a result of local pore water salinity increases induced by gas hydrate formation.
    Type: Article , PeerReviewed
    Format: text
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  • 2
    Publication Date: 2013-10-24
    Type: Conference or Workshop Item , NonPeerReviewed
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  • 3
    Publication Date: 2013-10-30
    Description: It is generally thought that the sulfate reduction metabolism is ancient and would have been established well before the Neoarchean. It is puzzling, therefore, that the sulfur isotope record of the Neoarchean is characterized by a signal of atmospheric mass-independent chemistry rather than a strong overprint by sulfate reducers. Here,...
    Keywords: Chemistry and Applications in Nature of Mass Independent Isotope Effects Special Feature
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 4
    Publication Date: 2013-12-31
    Description: The fossilization of organic remains and shell material by calcium phosphate minerals provides an illuminating, but time-bounded, window into Ediacaran–Cambrian animal evolution. For reasons that remain unknown, phosphatic fossil preservation declined significantly through Cambrian Series 2. Here, we investigate the phosphorus (P) sources for phosphatic Cambrian carbonates, presenting sedimentological, petrographic, and geochemical data from the Cambrian Series 2–3 Thorntonia Limestone, Australia, some of the youngest Cambrian strata to display exceptional phosphatic preservation of small shelly fossils. We find that within Thorntonia sediments, phosphate was remobilized by organic decay and bacterial iron reduction, with subsequent reprecipitation largely as apatite within the interiors of small shelly fossils. We discuss the merits of bioclastic-derived, organic matter–bound, or iron-bound P as potential sources to these strata. Petrographic observations suggest that the dissolution of phosphatic skeletal material did not provide the P for fossil preservation. In contrast, high organic carbon contents imply significant organic fluxes of P to Thorntonia sediments. Sedimentology and iron-speciation data indicate that phosphorus enrichment occurred during times of expanded anoxic, ferruginous conditions in subsurface water masses, suggesting that phosphorus adsorption to iron minerals precipitating from the water column provided a second significant P source to Thorntonia sediments. Simple stoichiometric models suggest that, by themselves, neither organic carbon burial nor an iron shuttle can account for the observed phosphorus enrichment. Thus, we infer that both processes were necessary for the observed phosphorus enrichment and subsequent fossil preservation in the Thorntonia Limestone.
    Print ISSN: 0016-7606
    Electronic ISSN: 1943-2674
    Topics: Geosciences
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  • 5
    Publication Date: 2015-10-20
    Description: The Cretaceous period (~145–65 m.y. ago) was characterized by intervals of enhanced organic carbon burial associated with increased primary production under greenhouse conditions. The global consequences of these perturbations, oceanic anoxic events (OAEs), lasted up to 1 m.y., but short-term nutrient and climatic controls on widespread anoxia are poorly understood. Here, we present a high-resolution reconstruction of oceanic redox and nutrient cycling as recorded in subtropical shelf sediments from Tarfaya, Morocco, spanning the initiation of OAE2. Iron-sulfur systematics and biomarker evidence demonstrate previously undescribed redox cyclicity on orbital time scales, from sulfidic to anoxic ferruginous (Fe-rich) water-column conditions. Bulk geochemical data and sulfur isotope modeling suggest that ferruginous conditions were not a consequence of nutrient or sulfate limitation, despite overall low sulfate concentrations in the proto–North Atlantic. Instead, fluctuations in the weathering influxes of sulfur and reactive iron, linked to a dynamic hydrological cycle, likely drove the redox cyclicity. Despite the potential for elevated phosphorus burial in association with Fe oxides under ferruginous conditions on the Tarfaya shelf, porewater sulfide generation drove extensive phosphorus recycling back to the water column, thus maintaining widespread open-ocean anoxia.
    Print ISSN: 0091-7613
    Electronic ISSN: 1943-2682
    Topics: Geosciences
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  • 6
    Publication Date: 2013-04-19
    Description: A significant body of evidence suggests that the marine environment remained largely anoxic throughout most of the Precambrian. In contrast, the oxygenation history of terrestrial aquatic environments has received little attention, despite the significance of such settings for early eukaryote evolution. To address this, we provide here a geochemical and isotopic assessment of sediments from the late Mesoproterozoic Nonesuch Formation of central North America. We utilize rhenium-osmium (Re-Os) geochronology to yield a depositional age of 1078 ± 24 Ma, while Os isotope compositions support existing evidence for a lacustrine setting. Fe-S-C systematics suggest that the Nonesuch Formation was deposited from an anoxic Fe-rich (ferruginous) water column. Thus, similar to the marine realm, anoxia persisted in terrestrial aquatic environments in the Middle to Late Proterozoic, but sulfidic water column conditions were not ubiquitous. Our data suggest that oxygenation of the terrestrial realm was not pervasive at this time and may not have preceded oxygenation of the marine environment, signifying a major requirement for further investigation of links between the oxygenation state of terrestrial aquatic environments and eukaryote evolution.
    Print ISSN: 0091-7613
    Electronic ISSN: 1943-2682
    Topics: Geosciences
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  • 7
    Publication Date: 2013-05-21
    Description: Nitrogen cycling has been evaluated across a depth transect in the late Paleoproterozoic Animikie Basin (North America), spanning the end of Earth’s final period of global iron precipitation, and a major transition to euxinic conditions in areas of high productivity. Sediments from near shore, where productivity was highest, have 15 N compositions up to ~3 higher than at more distal sites. This suggests that as NH 4 + mixed vertically upward into the oxic photic zone from the anoxic ocean interior, it was either assimilated by organisms or oxidized. Subsequent enhanced production of N 2 by denitrification or anammox (anaerobic ammonium oxidation) led to the observed increase in 15 N close to shore. Any deficit in biologically available N was overcome by N 2 -fixing organisms, but the input of N with low 15 N from this process did not overwhelm the increase in 15 N from denitrification. Because there is no evidence for conditions of severe N stress arising from trace metal limitation (particularly Mo) of N fixation during the transition to euxinic conditions, losses of N were either very small (potentially because low O 2 levels limited NH 4 + oxidation), or alternative pathways that retained N were important. The fact that Mo appears to have remained bioavailable for N fixation, either suggests that the extent or severity of sulfidic water column conditions was not sufficient to quantitatively sequester Mo on a global scale, or that rivers directly delivered Mo to surface waters on the inner shelf. The effects of N 2 fixation on 15 N increased to more distal parts of the shelf, consistent with models invoked for modern upwelling zones over broad continental margins.
    Print ISSN: 0091-7613
    Electronic ISSN: 1943-2682
    Topics: Geosciences
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  • 8
    Publication Date: 2016-11-19
    Description: Petroleum source rocks are strongly enriched in organic carbon (OC), and their trace metal (TM) contents often reach low-grade ore levels. The mechanisms leading to these coenrichments are important for understanding how extreme environmental conditions support the formation of natural resources. We therefore studied organic-rich Eocene marls and limestones (oil shale) from the central Jordan Amzaq-Hazra subbasin, part of a Cretaceous–Paleogene shelf system along the southern Neo-Tethys margin. Geochemical analyses on two cores show highly dynamic depositional conditions, consistent with sedimentological and micropaleontological observations. Maximum and average contents, respectively, in OC (~26 and ~10 wt%), sulfur (~7 and ~2.4 wt%), phosphorus (~10 and ~2 wt%), molybdenum (〉400 and ~130 ppm), chromium (〉500 and ~350 ppm), vanadium (〉1600 and ~550 ppm) and zinc (〉3800 and ~900 ppm) are exceptional, in particular without any indication of hydrothermal or epigenetic processes. We propose a combination of two processes: physical reworking of OC- and metal-rich material from locally exposed Cretaceous–Paleogene sediments (as supported by reworked nannofossils), and high marine productivity fueled by chemical remobilization of nutrients and metals on land that sustained anoxic-sulfidic conditions. Burial of high-quality organic matter (hydrogen index 600–700 mgHC/gOC) was related to strongly reducing conditions, punctuated by only short-lived oxygenation events, and to excess H 2 S, promoting organic matter sulfurization. These processes likely caused the OC and TM coenrichments in a high-energy shallow-marine setting that contradicts common models for black shale formation, but may explain similar geochemical patterns in other black shales.
    Print ISSN: 0091-7613
    Electronic ISSN: 1943-2682
    Topics: Geosciences
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  • 9
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 10
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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