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  • Elsevier  (3)
  • Malden, Mass. [u.a.] : Blackwell  (1)
  • 1
    Book
    Book
    Malden, Mass. [u.a.] : Blackwell
    Keywords: Geomicrobiology ; Geomicrobiology ; Einführung ; Geomikrobiologie ; Geomikrobiologie ; Biomineralisation ; Geomikrobiologie
    Type of Medium: Book
    Pages: X, 425, [8] S. , Ill., graph. Darst.
    Edition: 1. publ.
    ISBN: 0632054549 , 9780632054541
    DDC: 579
    RVK:
    RVK:
    Language: English
    Note: Includes bibliographical references and index
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  • 2
    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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  • 3
    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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  • 4
    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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