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  • Elsevier  (3)
  • Newark :John Wiley & Sons, Incorporated,  (2)
  • 1
    Online Resource
    Online Resource
    Newark :John Wiley & Sons, Incorporated,
    Keywords: Geomicrobiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (443 pages)
    Edition: 1st ed.
    ISBN: 9781444309027
    DDC: 579
    Language: English
    Note: Intro -- Preface -- 1 Microbial properties and diversity -- 1.1 Classification of life -- 1.2 Physical properties of microorganisms -- 1.2.1 Prokaryotes -- 1.2.2 Eukaryotes -- 1.3 Requirements for growth -- 1.3.1 Physical requirements -- 1.3.2 Chemical requirements -- 1.3.3 Growth rates -- 1.4 Microbial diversity -- 1.5 Life in extreme environments -- 1.5.1 Hydrothermal systems -- 1.5.2 Polar environments viable population is available to seed the global -- 1.5.3 Acid environments -- 1.5.4 Hypersaline and alkaline environments -- 1.5.5 Deep-subsurface environments -- 1.5.6 Life on other planets -- 1.5.7 Panspermia -- 1.6 Summary -- 2 Microbial metabolism -- 2.1 Bioenergetics -- 2.1.1 Enzymes -- 2.1.2 Oxidation-reduction -- 2.1.3 ATP generation -- 2.1.4 Chemiosmosis -- 2.2 Photosynthesis -- 2.2.1 Pigments -- 2.2.2 The light reactions - anoxygenic photosynthesis -- 2.2.3 Classification of anoxygenic photosynthetic bacteria -- 2.2.4 The light reactions - oxygenic photosynthesis -- 2.2.5 The dark reactions -- 2.2.6 Nitrogen fixation -- 2.3 Catabolic processes -- 2.3.1 Glycolysis and fermentation -- 2.3.2 Respiration -- 2.4 Chemoheterotrophic pathways -- 2.4.1 Aerobic respiration -- 2.4.2 Dissimilatory nitrate reduction -- 2.4.3 Dissimilatory manganese reduction -- 2.4.4 Dissimilatory iron reduction -- 2.4.5 Trace metal and metalloid reductions -- 2.4.6 Dissimilatory sulfate reduction -- 2.4.7 Methanogenesis and homoacetogenesis -- 2.5 Chemolithoautotrophic pathways -- 2.5.1 Hydrogen oxidizers -- 2.5.2 Homoacetogens and methanogens -- 2.5.3 Methylotrophs -- 2.5.4 Sulfur oxidizers -- 2.5.5 Iron oxidizers -- 2.5.6 Manganese oxidizers -- 2.5.7 Nitrogen oxidizers -- 3 Cell surface reactivity and metal sorption -- 3.1 The cell envelope -- 3.1.1 Bacterial cell walls -- 3.1.2 Bacterial surface layers -- 3.1.3 Archaeal cell walls. , 3.1.4 Eukaryotic cell walls -- 3.2 Microbial surface charge -- 3.2.1 Acid-base chemistry of microbial surfaces -- 3.2.2 Electrophoretic mobility -- 3.2.3 Chemical equilibrium models -- 3.3 Passive metal adsorption -- 3.3.1 Metal adsorption to bacteria -- 3.3.2 Metal adsorption to eukaryotes -- 3.3.3 Metal cation partitioning -- 3.3.4 Competition with anions -- 3.4 Active metal adsorption -- 3.4.1 Surface stability requirements -- 3.4.2 Metal binding to microbial exudates -- 3.5 Bacterial metal sorption models -- 3.5.1 Kd coefficients -- 3.5.2 Freundlich isotherms -- 3.5.3 Langmuir isotherms -- 3.5.4 Surface complexation -- 3.5.5 Does a generalized sorption model exist? -- 3.6 The microbial role in contaminant mobility -- 3.6.1 Microbial sorption to solid surfaces -- 3.6.2 Microbial transport through porous media -- 3.7 Industrial applications based on microbial surface reactivity -- 3.7.1 Bioremediation -- 3.7.2 Biorecovery -- 3.8 Summary -- 4 Biomineralization -- 4.1 Biologically induced mineralization -- 4.1.1 Mineral nucleation and growth -- 4.1.2 Iron hydroxides -- 4.1.3 Magnetite -- 4.1.4 Manganese oxides -- 4.1.5 Clays -- 4.1.6 Amorphous silica -- 4.1.7 Carbonates -- 4.1.8 Phosphates -- 4.1.9 Sulfates -- 4.1.10 Sulfide minerals -- 4.2 Biologically controlled mineralization -- 4.2.1 Magnetite -- 4.2.2 Greigite -- 4.2.3 Amorphous silica -- 4.2.4 Calcite -- 4.3 Fossilization -- 4.3.1 Silicification -- 4.3.2 Other authigenic minerals -- 4.4 Summary -- 5 Microbial weathering -- 5.1 Mineral dissolution -- 5.1.1 Reactivity at mineral surfaces -- 5.1.2 Microbial colonization and organic reactions -- 5.1.3 Silicate weathering -- 5.1.4 Carbonate weathering -- 5.1.5 Soil formation -- 5.1.6 W eathering and global climate -- 5.2 Sulfide oxidation -- 5.2.1 Pyrite oxidation mechanisms -- 5.2.2 Biological role in pyrite oxidation -- 5.2.3 Bioleaching. , 5.2.4 Biooxidation of refractory gold -- 5.3 Microbial corrosion -- 5.3.1 Chemolithoautotrophs -- 5.3.2 Chemoheterotrophs -- 5.3.3 Fungi -- 5.4 Summary -- 6 Microbial zonation -- 6.1 Microbial mats -- 6.1.1 Mat development -- 6.1.2 Photosynthetic mats -- 6.1.3 Chemolithoautotrophic mats -- 6.1.4 Biosedimentary structures -- 6.2 Marine sediments -- 6.2.1 Organic sedimentation -- 6.2.2 An overview of sediment diagenesis -- 6.2.3 Oxic sediments -- 6.2.4 Suboxic sediments -- 6.2.5 Anoxic sediments -- 6.2.6 Preservation of organic carbon Preservation of organic carbon -- 6.2.7 Diagenetic mineralization -- 6.2.8 Sediment hydrogen concentrations -- 6.2.9 Problems with the biogeochemical zone scheme -- 6.3 Summary -- 7 Early microbial life -- 7.1 The prebiotic Earth -- 7.1.1 The Hadean environment -- 7.1.2 Origins of life -- 7.1.3 Mineral templates -- 7.2 The first cellular life forms -- 7.2.1 The chemolithoautotrophs -- 7.2.2 Deepest-branching Bacteria and Archaea -- 7.2.3 The fermenters and initial respirers -- 7.3 Evolution of photosynthesis -- 7.3.1 Early phototrophs -- 7.3.2 Photosynthetic expansion -- 7.3.3 The cyanobacteria -- 7.4 Metabolic diversification -- 7.4.1 Obligately anaerobic respirers -- 7.4.2 Continental platforms as habitats -- 7.4.3 Aerobic respiratory pathways -- 7.5 Earth's oxygenation -- 7.5.1 The changing Proterozoic environment -- 7.5.2 Eukaryote evolution -- 7.6 Summary -- References -- Index.
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  • 2
    Online Resource
    Online Resource
    Newark :John Wiley & Sons, Incorporated,
    Keywords: Geobiology. ; Biosphere. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (481 pages)
    Edition: 1st ed.
    ISBN: 9781118280867
    DDC: 508
    Language: English
    Note: Intro -- FUNDAMENTALS OF GEOBIOLOGY -- Contents -- Contributors -- 1. What is Geobiology? -- 1.1 Introduction -- 1.2 Life interacting with the Earth -- 1.3 Pattern and process in geobiology -- 1.4 New horizons in geobiology -- References -- 2. The Global Carbon Cycle: Biological Processes -- 2.1 Introduction -- 2.2 A brief primer on redox reactions -- 2.3 Carbon as a substrate for biological reactions -- 2.4 The evolution of photosynthesis -- 2.5 The evolution of oxygenic phototrophs -- 2.6 Net primary production -- 2.7 What limits NPP on land and in the ocean? -- 2.8 Is NPP in balance with respiration? -- 2.9 Conclusions and extensions -- References -- 3. The Global Carbon Cycle: Geological Processes -- 3.1 Introduction -- 3.2 Organic carbon cycling -- 3.3 Carbonate cycling -- 3.4 Mantle degassing -- 3.5 Metamorphism -- 3.6 Silicate weathering -- 3.7 Feedbacks -- 3.8 Balancing the geological carbon cycle -- 3.9 Evolution of the geological carbon cycle through Earth's history: proxies and models -- 3.10 The geological C cycle through time -- 3.11 Limitations and perspectives -- References -- 4. The Global Nitrogen Cycle -- 4.1 Introduction -- 4.2 Geological nitrogen cycle -- 4.3 Components of the global nitrogen cycle -- 4.4 Nitrogen redox chemistry -- 4.5 Biological reactions of the nitrogen cycle -- 4.6 Atmospheric nitrogen chemistry -- 4.7 Summary and areas for future research -- References -- 5. The Global Sulfur Cycle -- 5.1 Introduction -- 5.2 The global sulfur cycle from two perspectives -- 5.3 The evolution of S metabolisms -- 5.4 The interaction of S with other biogeochemical cycles -- 5.5 The evolution of the S cycle -- 5.6 Closing remarks -- Acknowledgements -- References -- 6. The Global Iron Cycle -- 6.1 Overview -- 6.2 The inorganic geochemistry of iron: redox and reservoirs -- 6.3 Iron in modern biology and biogeochemical cycles. , 6.4 Iron through time -- 6.5 Summary -- Acknowledgements -- References -- 7. The Global Oxygen Cycle -- 7.1 Introduction -- 7.2 The chemistry and biochemistry of oxygen -- 7.3 The concept of redox balance -- 7.4 The modern O2 cycle -- 7.5 Cycling of O2 and H2 on the early Earth -- 7.6 Synthesis: speculations about the timing and cause of the rise of atmospheric O2 -- References -- 8. Bacterial Biomineralization -- 8.1 Introduction -- 8.2 Mineral nucleation and growth -- 8.3 How bacteria facilitate biomineralization -- 8.4 Iron oxyhydroxides -- 8.5 Calcium carbonates -- Acknowledgements -- References -- 9. Mineral-Organic-Microbe Interfacial Chemistry -- 9.1 Introduction -- 9.2 The mineral surface (and mineral-bio interface) and techniques for its study -- 9.3 Mineral-organic-microbe interfacial processes: some key examples -- Acknowledgements -- References -- 10. Eukaryotic Skeletal Formation -- 10.1 Introduction -- 10.2 Mineralization by unicellular organisms -- 10.3 Mineralization by multicellular organisms -- 10.4 A brief history of skeletons -- 10.5 Summary -- Acknowledgements -- References -- 11. Plants and Animals as Geobiological Agents -- 11.1 Introduction -- 11.2 Land plants as geobiological agents -- 11.3 Animals as geobiological agents -- 11.4 Conclusions -- Acknowledgements -- References -- 12. A Geobiological View of Weathering and Erosion -- 12.1 Introduction -- 12.2 Effects of biota on weathering -- 12.3 Effects of organic molecules on weathering -- 12.4 Organomarkers in weathering solutions -- 12.5 Elemental profiles in regolith -- 12.6 Time evolution of profile development -- 12.7 Investigating chemical, physical, and biological weathering with simple models -- 12.8 Conclusions -- Acknowledgements -- References -- 13. Molecular Biology's Contributions to Geobiology -- 13.1 Introduction -- 13.2 Molecular approaches used in geobiology. , 13.3 Case study: anaerobic oxidation of methane -- 13.4 Challenges and opportunities for the next generation -- Acknowledgements -- References -- 14. Stable Isotope Geobiology -- 14.1 Introduction -- 14.2 Isotopic notation and the biogeochemical elements -- 14.3 Tracking fractionation in a system -- 14.4 Applications -- 14.5 Using isotopes to ask a geobiological question in deep time -- 14.6 Conclusions -- Acknowledgements -- References -- 15. Biomarkers: Informative Molecules for Studies in Geobiology -- 15.1 Introduction -- 15.2 Origins of biomarkers -- 15.3 Diagenesis -- 15.4 Isotopic compositions -- 15.5 Stereochemical considerations -- 15.6 Lipid biosynthetic pathways -- 15.7 Classification of lipids -- 15.8 Lipids diagnostic of Archaea -- 15.9 Lipids diagnostic of Bacteria -- 15.10 Lipids of Eukarya -- 15.11 Preservable cores -- 15.12 Outlook -- Acknowledgements -- References -- 16. The Fossil Record of Microbial Life -- 16.1 Introduction -- 16.2 The nature of Earth's early microbial record -- 16.3 Paleobiological inferences from microfossil morphology -- 16.4 Inferences from microfossil chemistry and ultrastructure (new technologies) -- 16.5 Inferences from microbialites -- 16.6 A brief history, with questions -- 16.7 Conclusions -- Acknowledgements -- References -- 17. Geochemical Origins of Life -- 17.1 Introduction -- 17.2 Emergence as a unifying concept in origins research -- 17.3 The emergence of biomolecules -- 17.4 The emergence of macromolecules -- 17.5 The emergence of self-replicating systems -- 17.6 The emergence of natural selection -- 17.7 Three scenarios for the origins of life -- Acknowledgements -- References -- 18. Mineralogical Co-evolution of the Geosphere and Biosphere -- 18.1 Introduction -- 18.2 Prebiotic mineral evolution I - evidence from meteorites -- 18.3 Prebiotic mineral evolution II - crust and mantle reworking. , 18.4 The anoxic Archean biosphere -- 18.5 The Great Oxidation Event -- 18.6 A billion years of stasis -- 18.7 The snowball Earth -- 18.8 The rise of skeletal mineralization -- 18.9 Summary -- Acknowledgements -- References -- 19. Geobiology of the Archean Eon -- 19.1 Introduction -- 19.2 Carbon cycle -- 19.3 Sulfur cycle -- 19.4 Iron cycle -- 19.5 Oxygen cycle -- 19.6 Nitrogen cycle -- 19.7 Phosphorus cycle -- 19.8 Bioaccretion of sediment -- 19.9 Bioalteration -- 19.10 Conclusions -- References -- 20. Geobiology of the Proterozoic Eon -- 20.1 Introduction -- 20.2 The Great Oxidation Event -- 20.3 The early Proterozoic: Era geobiology in the wake of the GOE -- 20.4 The mid-Proterozoic: a last gasp of iron formations, deep ocean anoxia, the 'boring' billion, and a mid-life crisis -- 20.5 The history of Proterozoic life: biomarker records -- 20.6 The history of Proterozoic life: mid-Proterozoic fossil record -- 20.7 The late Proterozoic: a supercontinent, oxygen, ice, and the emergence of animals -- 20.8 Summary -- Acknowledgements -- References -- 21. Geobiology of the Phanerozoic -- 21.1 The beginning of the Phanerozoic Eon -- 21.2 Cambrian mass extinctions -- 21.3 The terminal Ordovician mass extinction -- 21.4 The impact of early land plants -- 21.5 Silurian biotic crises -- 21.6 Devonian mass extinctions -- 21.7 Major changes of the global ecosystem in Carboniferous time -- 21.8 Low-elevation glaciation near the equator -- 21.9 Drying of climates -- 21.10 A double mass extinction in the Permian -- 21.11 The absence of recovery in the early Triassic -- 21.12 The terminal Triassic crisis -- 21.13 The rise of atmospheric oxygen since early in Triassic time -- 21.14 The Toarcian anoxic event -- 21.15 Phytoplankton, planktonic foraminifera, and the carbon cycle -- 21.16 Diatoms and the silica cycle -- 21.17 Cretaceous climates. , 21.18 The sudden Paleocene-Eocene climatic shift -- 21.19 The cause of the Eocene-Oligocene climatic shift -- 21.20 The re-expansion of reefs during Oligocene time -- 21.21 Drier climates and cascading evolutionary radiations on the land -- References -- 22. Geobiology of the Anthropocene -- 22.1 Introduction -- 22.2 The Anthropocene -- 22.3 When did the Anthropocene begin? -- 22.4 Geobiology and human population -- 22.5 Human appropriation of the Earth -- 22.6 The carbon cycle and climate of the Anthropocene -- 22.7 The future of geobiology -- Acknowledgements -- References -- Index -- Colour plates.
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  • 3
    Publication Date: 2018-12-17
    Description: The Boolgeeda Iron Formation and overlying Turee Creek Group, Hamersley Basin, Western Australia, represent a conformable succession of sediment deposited between 2.45 and 2.22 Ga. This interval of geologic history is of significant interest because it spans the Great Oxidation Event (GOE), when oxygen first accumulated in Earth’s atmosphere. Here we present geochemical and petrographic data from the uppermost 45 m of the Boolgeeda Iron Formation and an additional 30 m of the overlying Kungarra Formation mudstones, as sampled from the Turee Creek Drilling Project 1 drill core (TCDP1). This core captures the termination of BIF deposition in the Hamersley Basin and coincides with a global decline in BIF deposition in the Paleoproterozoic. We provide a continuous, high resolution chemostratigraphic dataset of major and trace element concentrations, as well as Fe speciation data, to assess the relationship between the rise of atmospheric oxygen and the subsequent decline in BIF deposition. We also highlight the interplay between local and global controls on the preservation of redox signatures, including the rise and fall of local base-level, input of weathered continental material, influx of reduced sulfur species associated with the continental weathering, and global increases in atmospheric oxygen. We interpret Boolgeeda deposition to have taken place under shallow water, oxic conditions overlying anoxic ferruginous deep water. Intermittent periods of oxidative weathering led to influxes of redox sensitive trace elements from land as continental sulfide minerals were weathered. This also led to the temporary disappearance of MIF-S, but O2 remained below the threshold capable of completely eliminating S isotope signatures associated with the MIF-S recycling.
    Type: Article , PeerReviewed
    Format: text
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  • 4
    Publication Date: 2022-01-31
    Description: Highlights • The adsorption of Co, Ni, Cu, and Zn to Synechococcus sp PCC 7002 was studied using a surface complexation modelling approach. • A surface complexation model was developed to determine the thermodynamic binding constants of Co, Ni, Cu, and Zn to Synechococcus. • The surface complexation model was able to accurately predict the competitive adsorptionof the four metals to Synechococcus. • Synechococcus could have been an important exit channel for trace elements into ancient sediments such as BIF Marine bacterial plankton play a key role in elemental cycling through their ability to bind, assimilate, metabolize, and modify the redox state of trace metals in seawater. Of those processes, arguably the least studied are the mechanisms underpinning trace metal adsorption to planktonic marine bacteria, despite a plethora of literature pertaining to terrestrial species. Recently, Liu et al. (2015) demonstrated that the marine cyanobacterium Synechococcus sp. PCC 7002 has the capacity to remove appreciable amounts of Cd2+, a proxy for other divalent cations, from seawater by adsorption. In this study, we build on that work and employ a surface complexation modelling (SCM) approach using titration and pH adsorption edge experiments to calculate the thermodynamic binding constants of four bioessential transition metals (Co, Ni, Cu, Zn) to Synechococcus in simulated seawater. Based on the titration results, the major functional groups involved in metal binding were carboxyl groups with a pKa of 5.59 and phosphoryl groups with a pKa of 7.61. Metal adsorption experiments indicate that Synechococcus can bind considerable concentrations of Zn, Cu, Ni, and Co at pH 8. When all four metals are simultaneously added to solution, the same adsorption pattern of Zn 〉 Cu 〉 Ni 〉 Co is maintained, and accurately predicted by the SCM. Based on average marine cell densities and turnover rates of Synechococcus cells in the photic zone, we calculate that Synechococcus, in the absence of competing ligands such as dissolved organic matter (DOM), has the theoretical capacity to remove nearly all of the free metal cations from seawater. These observations highlight the surface reactivity of marine cyanobacteria as a potentially important vector for the transfer of dissolved metals from the photic zone to deeper waters or the seafloor in modernoceans, but they also have implications for the Precambrian oceans as sinking cyanobacteria could have acted as an exit channel for trace elements into ancient sediments including banded iron formations (BIF).
    Type: Article , PeerReviewed
    Format: text
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  • 5
    Publication Date: 2024-02-07
    Description: Highlights • The adsorption of Cd to Synechocystis sp. PCC 6803 was investigated at both marine and freshwater ionic strength. • The thermodynamic binding constants of Cd to Synechocystis were calculated using a surface complexation modeling approach. • Synechocystis and other planktonic cyanobacteria may be an important vector of trace metals transport to marine settings. Cyanobacteria are abundant in nearly every surface environment on Earth. Understanding their chemical reactivity and metal binding capacity with varying ionic strength (IS) is paramount to understanding trace metal cycling in natural environments. We conducted an investigation on the cell surface reactivity of the freshwater cyanobacterium Synechocystis sp. PCC 6803 at freshwater (0.01 M NaCl) and marine (0.56 M NaCl) IS. Potentiometric titration data were used to develop a multiple discrete site, non-electrostatic surface complexation model (SCM), and corresponding cell surface functional group identities were verified using attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Synechocystis cells were best modeled in FITEQL 4.0 using a non-electrostatic 2-site protonation model. Cadmium (Cd) adsorption experiments paired with SCM was utilized to calculate the binding constants of Cd. Synechocystis surface functional groups demonstrated a stronger affinity for Cd across the entire pH range studied (3–9) at freshwater IS, with the greatest difference at circumneutral pH (6–8) where Cd adsorption in freshwater IS was 60% greater than at marine IS. These data combined with the ubiquitous distribution of Synechocystis in freshwater and brackish environments suggest that these organisms could play an important role in trace metal cycling in environments with large salinity gradients, such as estuaries and deltas, and could act as a transport mechanism for trace metals from terrestrial to marine settings.
    Type: Article , PeerReviewed
    Format: text
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