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  • 1
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Hydrocarbons. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (691 pages)
    Edition: 1st ed.
    ISBN: 9783031056239
    Series Statement: Topics in Geobiology Series ; v.53
    DDC: 553.28
    Language: English
    Note: Intro -- Preface -- References -- Contents -- Contributors -- Part I: Biogeochemical Processes -- Chapter 1: Geochemistry of Cold Hydrocarbon Seeps: An Overview -- 1.1 Introduction -- 1.2 The Redox Cascade -- 1.3 Methane Oxidation -- 1.4 Seep Carbonate Formation -- 1.5 Iron and Sulfur Cycling at Seeps -- 1.6 Isotope Geochemistry of Cold Seeps -- 1.6.1 Carbon and Oxygen Isotopes in Seep Carbonates -- 1.6.2 Carbonate-Clumped Isotopes -- 1.6.3 C and O Isotopes in Shells of Seep Fauna -- 1.6.4 Strontium and Neodymium Isotopes -- 1.6.5 Sulfur Isotopes -- 1.7 Elemental Geochemistry of Cold Seeps -- 1.7.1 Rare Earth Elements -- 1.7.2 Non-lanthanide Elements -- 1.8 Summary -- Appendix -- References -- Chapter 2: Biomarkers in Ancient Hydrocarbon Seep Carbonates -- 2.1 Introduction -- 2.1.1 What Are Biomarkers? -- 2.1.2 Pioneer Studies on Biomarkers at Cold Seeps -- 2.2 Basic Guide to Biomarker Studies of Ancient Seeps -- 2.2.1 Sample Preparation, Lipid Extraction, and Analysis -- 2.2.2 Effects of Allochthonous Biomarkers, Thermal Maturity, and Biodegradation -- 2.3 Biomarkers of AOM-Performing Microbes -- 2.3.1 Biomarkers of ANME Archaea -- 2.3.2 Biomarkers of SRB Partners -- 2.4 Biomarkers of Aerobic Methanotrophs -- 2.5 Stable Carbon Isotope Signatures of Seep-Related Biomarkers -- 2.5.1 Carbon Isotopic Composition of ANME Biomarkers -- 2.5.2 Carbon Isotopic Composition of SRB Biomarkers -- 2.5.3 Carbon Isotopic Composition of Aerobic Methanotroph Biomarkers -- 2.6 AOM Community and Seep Environment -- 2.6.1 Factors Controlling the Distribution of AOM Communities -- 2.6.2 Micro-distribution of AOM Communities in Seep Carbonates -- 2.7 Future Outlook -- References -- Chapter 3: Ancient Seep Carbonates: From Outcrop Appearance to Microscopic Petrography -- 3.1 Introduction -- 3.2 Size of Seep Deposits -- 3.2.1 Extant Seep Deposits. , 3.2.2 Ancient Seep Deposits -- 3.3 Macroscopic Appearance -- 3.3.1 Extant Seep Carbonates -- 3.3.2 Ancient Seep Carbonates -- 3.4 Macroscopic Petrography -- 3.4.1 Extant Seep Carbonates -- 3.4.2 Ancient Seep Carbonates -- 3.5 Microscopic Petrography -- 3.5.1 Extant Seep Carbonates -- 3.5.2 Ancient Seep Carbonates -- 3.6 Concluding Remarks and Future Directions -- References -- Part II: Seep Biota -- Chapter 4: Microbes in Modern and Ancient Hydrocarbon Seeps -- 4.1 Introduction -- 4.2 Current Knowledge on Extant Systems -- 4.3 Paths to Fossilization (Taphonomy) -- 4.4 Microbial Fossil Record at Seeps -- 4.5 Search Strategy for Future Studies -- 4.5.1 Targeting Particular Petrofabrics -- 4.5.2 Utilization of More Focused Technologies -- 4.5.3 Connection with Clearer Geochemical Proxies -- 4.6 Conclusions -- References -- Chapter 5: Crustaceans in Cold Seep Ecosystems: Fossil Record, Geographic Distribution, Taxonomic Composition, and Biology -- 5.1 Introduction -- 5.2 Crustaceans in Fossil Cold Seeps: A Quantitative Analysis -- 5.3 Decapod Crustaceans -- 5.3.1 Modern Occurrences and Composition -- 5.3.2 Biology -- 5.3.3 Fossil Record and Evolution -- 5.3.3.1 Body Fossils -- 5.3.3.2 Burrows -- 5.3.3.3 Fecal Pellets -- 5.3.3.4 Repair Scars -- 5.4 Ostracods -- 5.4.1 Modern Occurrences and Composition -- 5.4.2 Biology -- 5.4.3 Fossil Record and Evolution -- 5.5 Barnacles -- 5.5.1 Modern Occurrences and Composition -- 5.5.2 Biology -- 5.5.3 Fossil Record and Evolution -- 5.6 Conclusions -- References -- Chapter 6: Non-calcareous Tubeworms in Ancient Hydrocarbon Seeps -- 6.1 Introduction -- 6.2 Non-calcareous Tubeworms -- 6.2.1 Family Siboglinidae -- 6.2.1.1 Overview -- 6.2.1.2 Biology -- 6.2.1.3 Fossil Record and Evolution -- 6.2.1.4 Classification and Tube Characters -- 6.2.2 Family Chaetopteridae -- 6.2.2.1 Overview -- 6.2.2.2 Biology. , 6.2.2.3 Fossil Record and Evolution -- 6.2.2.4 Classification and Tube Characters -- 6.3 Other Organic Tube Dwellers at Seeps -- 6.4 Agglutinated Tube Dwellers at Seeps -- 6.5 Conclusions -- References -- Chapter 7: Calcareous Tubeworms in Ancient Hydrocarbon Seeps -- 7.1 Introduction -- 7.2 Calcareous Tubeworms -- 7.2.1 Family Serpulidae -- 7.2.1.1 Overview -- 7.2.1.2 Biology -- 7.2.1.3 Fossil Record and Evolution -- 7.2.1.4 Classification and Tube Characters -- 7.3 Conclusions -- References -- Chapter 8: Brachiopods at Hydrocarbon Seeps -- 8.1 Introduction -- 8.2 Overview of Brachiopod Occurrences at Palaeozoic Hydrocarbon Seeps -- 8.2.1 Order: Lingulida Waagen, 1885 -- 8.2.2 Order: Rhynchonellida Kuhn, 1949 -- 8.2.3 Order: Atrypida Rzhonsnitskaia, 1960 -- 8.3 Overview of Brachiopod Occurrences at Mesozoic and Cenozoic Hydrocarbon Seeps -- 8.3.1 Lingulida Waagen, 1885 -- 8.3.2 Rhynchonellida Kuhn, 1949 -- 8.3.3 Order: Terebratulida Waagen, 1883 -- 8.4 Palaeoecological and Evolutionary Patterns: The Elusive Case of Brachiopod-Dominated Seep Communities -- 8.4.1 Ecological Constraints -- 8.4.2 Possible Controls on the Brachiopod Versus Bivalve Dominance at Seeps Over Time -- 8.4.2.1 Palaeogeographic Hypothesis and the Role of the Frasnian-Famennian Crisis -- 8.4.2.2 Feeding Strategy Hypothesis, with Constraints from Habitat Preferences and Background Seawater Sulphate Chemistry -- 8.5 Conclusions -- References -- Chapter 9: Extant and Fossil Sponges Associated with Hydrothermal Vent and Cold Seep Communities -- 9.1 Introduction -- 9.2 Porifera Grant, 1836 -- 9.2.1 Homoscleromorpha Bergquist, 1978 -- 9.2.2 Demospongiae Sollas, 1885 -- 9.2.3 Hexactinellida Schmidt, 1870 -- 9.2.4 Calcarea Bowerbank, 1862 -- 9.3 Extant Sponges Associated with Vent and Seep Communities -- 9.4 Fossil Sponges Associated with Vent and Seep Communities. , 9.4.1 Cambrian of China -- 9.4.2 Jurassic of France and Spitsbergen -- 9.4.3 Cretaceous (Campanian) of Hokkaido, Japan -- 9.4.4 Paleogene and Neogene of Oregon and Washington, USA -- 9.5 Discussion and Summary -- References -- Chapter 10: Bivalvia in Ancient Hydrocarbon Seeps -- 10.1 Introduction -- 10.2 Family Solemyidae -- 10.2.1 Fossil Record and Evolution -- 10.2.2 Classification and Shell Characters -- 10.3 Family Nucinellidae -- 10.3.1 Fossil Record and Evolution -- 10.3.2 Classification and Shell Characters -- 10.4 Family Mytilidae -- 10.4.1 Fossil Record and Evolution -- 10.4.2 Classification and Shell Characters -- 10.5 Families Modiomorphidae and Kalenteridae -- 10.5.1 Fossil Record and Evolution -- 10.5.2 Classification and Shell Characters -- 10.6 Family Lucinidae -- 10.6.1 Fossil Record and Evolution -- 10.6.2 Classification and Shell Characters -- 10.7 Family Thyasiridae -- 10.7.1 Fossil Record and Evolution -- 10.7.2 Classification and Shell Characteristics -- 10.8 Family Vesicomyidae -- 10.8.1 Fossil Record and Evolution -- 10.8.2 Classification and Shell Characters -- 10.9 The Anomalodesmata -- 10.10 Conclusions -- References -- Chapter 11: A Review of Gastropods at Ancient Hydrocarbon Seeps -- 11.1 Introduction -- 11.2 Abyssochrysoidea -- 11.2.1 Hokkaidoconchidae -- 11.2.2 Abyssochrysidae -- 11.2.3 Paskentanidae -- 11.2.4 Alviniconchinae New Subfamily -- 11.2.5 Desbruyeresidae New Family -- 11.2.6 Provannidae -- 11.2.7 Rubyspiridae New Family -- 11.3 Neomphalida -- 11.4 Limpets -- 11.4.1 Cocculinida -- 11.4.2 Lepetellida -- 11.4.3 Patellida -- 11.5 Trochomorph Vetigastropods -- 11.5.1 Seguenziida -- 11.5.2 Trochida -- 11.5.2.1 Colloniidae Cossmann in Cossmann and Peyrot, 1917 -- 11.6 Neritimorpha -- 11.7 Neogastropoda -- 11.7.1 Purpurinidae and Pseudotritonidae -- 11.7.2 Buccinoidea -- 11.7.3 Conoidea -- 11.7.4 Muricoidea. , 11.8 Heterobranchia -- 11.8.1 Cephalaspidea -- 11.8.2 Orbitestellidae -- 11.8.3 Hyalogyrinidae -- 11.8.4 Xylodisculidae -- 11.9 Other Groups -- 11.9.1 Rissoidae -- 11.9.2 Aporrhaidae -- 11.9.3 Ampullinidae and Naticidae -- 11.9.4 Eulimidae -- 11.10 Conclusions and Future Directions -- References -- Chapter 12: Ammonites as Inhabitants of Ancient Hydrocarbon Seeps -- 12.1 Introduction -- 12.2 Ammonite Paleobiology -- 12.3 Methane Seep Deposits -- 12.3.1 Antarctica -- 12.3.2 Argentina -- 12.3.3 Canadian Arctic -- 12.3.4 England -- 12.3.5 France -- 12.3.6 Greenland -- 12.3.7 Japan -- 12.3.8 Morocco -- 12.3.9 New Zealand -- 12.3.10 Novaya Zemlya -- 12.3.11 Oregon, USA -- 12.3.12 Spitsbergen (Svalbard) -- 12.3.13 Turkey -- 12.3.14 Western Interior, USA -- 12.4 Conclusions -- Appendix -- References -- Chapter 13: Echinoderms at Ancient Hydrocarbon Seeps and Cognate Communities -- 13.1 Introduction -- 13.2 Occurrences -- 13.2.1 Antarctica -- 13.2.2 England -- 13.2.3 France -- 13.2.4 Germany -- 13.2.5 Greenland -- 13.2.6 Italy -- 13.2.7 Japan -- 13.2.8 Morocco -- 13.2.9 Namibia -- 13.2.10 New Zealand -- 13.2.11 Novaya Zemlya -- 13.2.11.1 Poland -- 13.2.12 Svalbard -- 13.2.13 Turkey -- 13.2.14 Washington State, USA -- 13.2.15 Western Interior, USA -- 13.3 Conclusions -- Appendix -- References -- Chapter 14: Vertebrates: Skate and Shark Egg Capsules at Ancient Hydrocarbon Seeps -- 14.1 Overview and Examples -- References -- Part III: Fossil Seep Ecosystems -- Chapter 15: Methane Seeps in the Late Cretaceous Western Interior Seaway, USA -- 15.1 Introduction -- 15.2 Geologic Setting -- 15.3 Geomorphology of Seep Deposits -- 15.4 Geographic Distribution -- 15.5 Stratigraphic Distribution -- 15.6 Methods of Study -- 15.7 Oxygen and Carbon Isotopic Composition -- 15.8 Origin of Methane -- 15.9 Seep Duration -- 15.10 Seep Structure and Faunal Distribution. , 15.11 Faunal Composition.
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  • 2
    Online Resource
    Online Resource
    Cham : Springer International Publishing | Cham : Imprint: Springer
    Keywords: Physical geography. ; Paleoecology. ; Evolution (Biology). ; Geochemistry. ; Meeressediment ; Hydrothermalquelle ; Cold Seep ; Fossil ; Fossile Tiere ; Paläontologie ; Meeresökosystem ; Fossil ; Geoökosystem ; Palökologie ; Kohlenwasserstoffe
    Description / Table of Contents: Chapter 1-Introduction -- Chapter 2-Biogeochemical processes -- Chapter 3-Taphonomy and diagenesis of seeps -- Chapter 4-Biota -- Chapter 5-Seeps around the world -- Chapter 6-Seeps as ecosystems -- Chapter 7-Evolution of seep communities over geological time -- Chapter 8-Cognate communities.
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource(XVII, 687 p. 129 illus., 71 illus. in color.)
    Edition: 1st ed. 2022.
    ISBN: 9783031056239
    Series Statement: Topics in Geobiology 50
    Language: English
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  • 3
    Publication Date: 2022-05-26
    Description: © The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Horowitz, E. J., Cochran, J. K., Bacon, M. P., & Hirschberg, D. J. 210Po and 210Pb distributions during a phytoplankton bloom in the North Atlantic: implications for POC export. Deep-Sea Research Part I: Oceanographic Research Papers, 164, (2020): 103339, doi:10.1016/j.dsr.2020.103339.
    Description: During the North Atlantic Bloom Experiment (NABE) of the Joint Global Ocean Flux Study (JGOFS), water column sampling for particulate and dissolved 210Po and 210Pb was performed four times (26 April and 4, 20, 30 May 1989) during a month-long Lagrangian time-series occupation of the NABE site, as well as one-time samplings at stations during transit to and from the site. There are few prior studies documenting short-term changes in 210Po and 210Pb profiles over the course of a phytoplankton bloom, and we interpret the profiles in terms of the classical “steady-state” (SS) approach used in most studies, as well as by using a non-steady state approach suggested by the temporal evolution of the profiles. Changes in 210Po profiles during a bloom are expectable as this radionuclide is scavenged and exported. During NABE, 210Pb profiles also displayed non-steady state, with significant increases in upper water column inventory occurring midway through the experiment. Export of 210Po from the upper 150 m using the classic “steady-state” model shows increases from 0.5 ± 8.5 dpm m−2 d−1 to 68.2 ± 4.2 dpm m−2 d−1 over the ~one-month occupation. Application of a non-steady state model, including changes in both 210Pb and 210Po profiles, gives higher 210Po export fluxes. Detailed depth profiles of particulate organic carbon (〉0.8 μm) and particulate 210Po (〉0.4 μm) are available from the 20 and 30 May samplings and show maxima in POC/Po at ~37 m. Applying the POC/210Po ratios at 150 m to the “steady state” 210Po fluxes yields POC export from the upper 150 m of 8.2 ± 1.5 mmol C m− 2 d−1 on 20 May and 6.0 ± 1.6 mmol C m−2 d−1 on 30 May. The non-steady state model applied to the interval 20 to 30 May yields POC export of 24.3 mmol C m−2 d−1. The non-steady state (NSS) 210Po-derived POC fluxes are comparable to, but somewhat less than, those estimated previously from 234Th/238U disequilibrium for the same time interval (37.3 and 45.0 mmol m−2 d−1, depending on the POC/Th ratio used). In comparison, POC fluxes measured with a floating sediment trap deployed at 150 m from 20 to 30 May were 11.6 mmol m−2 d−1. These results suggest that non-steady state Po-derived POC fluxes during the NABE agree well with those derived from 234Th/238U disequilibrium and agree with sediment trap fluxes within a factor of ~2. However, unlike the 234Th-POC flux proxy, non-steady stage changes in profiles of 210Pb, the precursor of 210Po, must be considered.
    Description: We are grateful to T. Hammar and A. Fleer (WHOI) for assistance at sea and in the laboratory. This work was supported originally by National Science Foundation (United States) grant OCE-8819544 to JKC and more recently by OCE-1736591. We thank Stephen Thurston (American Museum of Natural History) for graphics assistance Robert Aller, Steven Beaupre, and two anonymous reviewers for helpful comments.
    Keywords: Polonium-210 ; Lead-210 ; 210Po ; 210Pb ; North Atlantic ; Spring bloom ; POC flux
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 4
    Publication Date: 2018-03-09
    Description: A mass balance for the naturally-occurring radium isotopes (224Ra, 223Ra, 228Ra, and 226Ra) in Jamaica Bay, NY, was conducted by directly estimating the individual Ra contributions of wastewater discharge, diffusion from fine-grained subtidal sediments, water percolation through marshes, desorption from resuspended particles, and water exchange at the inlet. The mass balance revealed a major unknown source term accounting for 19–71% of the total Ra input, which could only be resolved by invoking a source from submarine groundwater. Shallow (〈 2 m depth) groundwater from permeable sediments in Jamaica Bay was brackish and enriched in Ra relative to surface bay waters by over two orders of magnitude. To balance Ra fluxes, a submarine groundwater input of 0.8 × 109–9.0 × 109 L d− 1 was required. This flux was similar for all four isotopes, with individual estimates varying by less than a factor of 2. Our calculated groundwater flux was 6- to 70-fold higher than the fresh groundwater discharge to the bay estimated by hydrological methods, but closely matched direct flow rates measured with seepage meters. This suggests that a substantial portion of the discharge consisted of recirculated seawater. The magnitude of submarine groundwater discharge varied seasonally, in the order: summer 〉 autumn 〉 spring. Chemical analyses suggest that the recirculated seawater component of submarine groundwater delivers as much dissolved nitrogen to the bay as the fresh groundwater flux.
    Type: Article , PeerReviewed
    Format: text
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  • 5
    Publication Date: 2020-03-20
    Description: The MedFlux project was devised to determine and model relationships between organic matter and mineral ballasts of sinking particulate matter in the ocean. Specifically we investigated the ballast ratio hypothesis, tested various commonly used sampling and modeling techniques, and developed new technologies that would allow better characterization of particle biogeochemistry. Here we describe the rationale for the project, the biogeochemical provenance of the DYFAMED site, the international support structure, and highlights from the papers published here. Additional MedFlux papers can be accessed at the MedFlux web site (http://msrc.sunysb.edu/MedFlux/).
    Type: Article , PeerReviewed
    Format: text
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  • 6
    Publication Date: 2023-02-08
    Description: Glacial meltwater is an important source of bioessential trace elements to high latitude oceans. Upon delivery to coastal waters, glacially sourced particulate trace elements are processed during early diagenesis in sediments and may be sequestered or recycled back to the water column depending on local biogeochemical conditions. In the glaciated fjords of Svalbard, large amounts of reactive Fe and Mn (oxyhydr)oxides are delivered to the sediment by glacial discharge, resulting in pronounced Fe and Mn cycling concurrent with microbial sulfate reduction. In order to investigate the diagenetic cycling of selected trace elements (As, Co, Cu, Mo, Ni, and U) in this system, we collected sediment cores from two Svalbard fjords, Van Keulenfjorden and Van Mijenfjorden, in a transect along the head-to-mouth fjord axis and analyzed aqueous and solid phase geochemistry with respect to trace elements, sulfur, and carbon along with sulfate reduction rates. We found that Co and Ni associate with Fe and Mn (oxyhydr)oxides and enter the pore water upon reductive metal oxide dissolution. Copper is enriched in the solid phase where sulfate reduction rates are high, likely due to reactions with H2S and the formation of sulfide minerals. Uranium accumulates in the solid phase likely following reduction by both Fe- and sulfate-reducing bacteria, while Mo adsorbs to Fe and Mn (oxyhydr)oxides in the surface sediment and is removed from the pore water at depth where sulfidization makes it particle-reactive. Arsenic is tightly coupled to Fe redox cycling and its partitioning between solid and dissolved phases is influenced by competition with FeS for adsorption sites on crystalline Fe oxides. Differences in trace element cycling between the two fjords suggest delivery of varying amount and composition of tidewater glacier (Van Keulenfjorden) and meltwater stream (Van Mijenfjorden) material, likely related to oxidative processes occurring in meltwater streams. This processing produces a partially weathered, more reactive sediment that is subject to stronger redox cycling of Fe, Mn, S, and associated trace elements upon delivery to Van Mijenfjorden. With climate warming, the patterns of trace element cycling observed in Van Mijenfjorden may also become more prevalent in other Svalbard fjords as tidewater glaciers retreat into meltwater stream valleys.
    Type: Article , PeerReviewed
    Format: text
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