98 research outputs found

    Microbial communities in dark oligotrophic volcanic ice cave ecosystems of Mt. Erebus, Antarctica.

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    The Earth's crust hosts a subsurface, dark, and oligotrophic biosphere that is poorly understood in terms of the energy supporting its biomass production and impact on food webs at the Earth's surface. Dark oligotrophic volcanic ecosystems (DOVEs) are good environments for investigations of life in the absence of sunlight as they are poor in organics, rich in chemical reactants and well known for chemical exchange with Earth's surface systems. Ice caves near the summit of Mt. Erebus (Antarctica) offer DOVEs in a polar alpine environment that is starved in organics and with oxygenated hydrothermal circulation in highly reducing host rock. We surveyed the microbial communities using PCR, cloning, sequencing and analysis of the small subunit (16S) ribosomal and Ribulose-1,5-bisphosphate Carboxylase/Oxygenase (RubisCO) genes in sediment samples from three different caves, two that are completely dark and one that receives snow-filtered sunlight seasonally. The microbial communities in all three caves are composed primarily of Bacteria and fungi; Archaea were not detected. The bacterial communities from these ice caves display low phylogenetic diversity, but with a remarkable diversity of RubisCO genes including new deeply branching Form I clades, implicating the Calvin-Benson-Bassham (CBB) cycle as a pathway of CO2 fixation. The microbial communities in one of the dark caves, Warren Cave, which has a remarkably low phylogenetic diversity, were analyzed in more detail to gain a possible perspective on the energetic basis of the microbial ecosystem in the cave. Atmospheric carbon (CO2 and CO), including from volcanic emissions, likely supplies carbon and/or some of the energy requirements of chemoautotrophic microbial communities in Warren Cave and probably other Mt. Erebus ice caves. Our work casts a first glimpse at Mt. Erebus ice caves as natural laboratories for exploring carbon, energy and nutrient sources in the subsurface biosphere and the nutritional limits on life

    Impact of microbial Mn oxidation on the remobilization of bioreduced U(IV)

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    Effects of Mn redox cycling on the stability of bioreduced U(IV) are evaluated here. U(VI) can be biologically reduced to less soluble U(IV) species and the stimulation of biological activity to that end is a salient remediation strategy; however, the stability of these materials in the subsurface environments where they form remains unproven. Manganese oxides are capable of rapidly oxidizing U(IV) to U(VI) in mixed batch systems where the two solid phases are in direct contact. However, it is unknown whether the same oxidation would take place in a porous medium. To probe that question, U(IV) immobilized in agarose gels was exposed to conditions allowing biological Mn(II) oxidation (HEPES buffer, Mn(II), 5% O-2 and Bacillus sp. SG-1 spores). Results show the oxidation of U(IV) to U(VI) is due primarily to O-2 rather than to MnO2. U(VI) produced is retained within the gel to a greater extent when Mn oxides are present, suggesting the formation of strong surface complexes. The implication for the long-term stability of U in a bioremediated site is that, in the absence of competing ligands, biological Mn(II) oxidation may promote the immobilization of U(VI) produced by the oxidation of U(IV)

    Silica Biomineralization of Calothrix-Dominated Biofacies from Queen\u27s Laundry Hot-Spring, Yellowstone National Park, USA

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    Experiments on microorganisms capable of surviving silicification are often conducted to gain a better understanding of the process of silica biomineralization and to gain insights into microbially influenced rock formations and biofabrics like those found in ancient deposits such as the Early Archean Apex Chert formation (Schopf, 1993; House et al., 2000). An ideal microorganism for studying silicification is the large sheathed cyanobacterium Calothrix, which form distinctive organo-sedimentary structures in the low to moderate temperature regions of hydrothermal springs or columnar stromatolitic structures in aquatic systems. Our ability to identify and characterize microfossils from ancient deposits allows us to gain a better understanding of environmental conditions on early Earth. Here we characterized Calothrix-dominated biofacies along the outflow apron of Queen\u27s Laundry Hot-Spring in Yellowstone National Park using microscopy and molecular techniques to examine biofacies morphology and phylogenetic diversity. We found that flow regime and temperature had a profound effect on community composition as identified by the observation of five distinct Calothrix-dominated communities and on biofacies architecture along the outflow apron

    Silica Biomineralization of Calothrix-Dominated Biofacies from Queen\u27s Laundry Hot-Spring, Yellowstone National Park, USA

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    Experiments on microorganisms capable of surviving silicification are often conducted to gain a better understanding of the process of silica biomineralization and to gain insights into microbially influenced rock formations and biofabrics like those found in ancient deposits such as the Early Archean Apex Chert formation (Schopf, 1993; House et al., 2000). An ideal microorganism for studying silicification is the large sheathed cyanobacterium Calothrix, which form distinctive organo-sedimentary structures in the low to moderate temperature regions of hydrothermal springs or columnar stromatolitic structures in aquatic systems. Our ability to identify and characterize microfossils from ancient deposits allows us to gain a better understanding of environmental conditions on early Earth. Here we characterized Calothrix-dominated biofacies along the outflow apron of Queen\u27s Laundry Hot-Spring in Yellowstone National Park using microscopy and molecular techniques to examine biofacies morphology and phylogenetic diversity. We found that flow regime and temperature had a profound effect on community composition as identified by the observation of five distinct Calothrix-dominated communities and on biofacies architecture along the outflow apron

    Uranium speciation and stability after reductive immobilization in sediments

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    It has generally been assumed that the bioreduction of hexavalent uranium in groundwater systems will result in the precipitation of immobile uraninite (UO2). In order to explore the form and stability of uranium immobilized under these conditions, we introduced lactate (15 mM for 3 months) into flow-through columns containing sediments derived from a former uranium-processing site at Old Rifle, CO. This resulted in metal-reducing conditions as evidenced by concurrent uranium uptake and iron release. Despite initial augmentation with Shewanella oneidensis, bacteria belonging to the phylum Firmicutes dominated the biostimulated columns. The immobilization of uranium (similar to 1 mmol U per kg sediment) enabled analysis by Xray absorption spectroscopy (XAS). Tetravalent uranium associated with these sediments did not have spectroscopic signatures representative of U-U shells or crystalline UO2. Analysis by microfocused XAS revealed concentrated micrometer regions of solid U(IV) that had spectroscopic signatures consistent with bulk analyses and a poor proximal correlation (mu m scale resolution) between U and Fe. A plausible explanation, supported by biogeochemical conditions and spectral interpretations, is uranium association with phosphoryl moieties found in biomass; hence implicating direct enzymatic uranium reduction. After the immobilization phase, two months of in situ exposure to oxic influent did not result in substantial uranium remobilization. Ex situ flow-through experiments demonstrated more rapid uranium mobilization than observed in column oxidation studies and indicated that sediment-associated U(IV) is more mobile than biogenic UO2. This work suggests that in situ uranium bioimmobilization studies and subsurface modeling parameters should be expanded to account for non-uraninite U(IV) species associated with biomass. (C) 2011 Elsevier Ltd. All rights reserved
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