Microbes and mineral precipitation, Miette Hot Springs, Jasper National Park, Alberta, Canada

2003 ◽  
Vol 40 (11) ◽  
pp. 1483-1500 ◽  
Author(s):  
Sandy Bonny ◽  
Brian Jones

At Miette Hot Springs, SO42–/H2S-, Ca2+-, Sr2+-, and CO32–-rich waters with a mean temperature of 51.2 °C are ejected from three spring vents and several minor seeps near the floor of Sulphur Creek valley. Runoff channels from the springs are colonized by cyanobacteria (Oscillatoria, Phormidium, Gloeocapsa, Synechococcus, Xenococcus) that grow in resistant mats and as loose filaments within 0.5 m of the spring vents, diatom assemblages (Cymbella, Mastagloia, Brachysira, Sellaphora, Rhopalodia, Nitzschia, Navicula, Pinnularia) that dominate the flow paths 0.5–2.0 m from the vents, and microbial mats with cyanobacteria and diatoms in the distal flow paths. Sulphate-reducing bacteria and green algae are also present. Gypsum, elemental sulphur, and lesser quantities of calcite and strontianite precipitate from the spring waters. Microbial populations influence accumulation of mineral precipitates by (i) forming mats close to the spring vents on which crystals grow, (ii) forming mats alongside the flow paths that trap and bind precipitates, and (iii) providing loose filaments to which microscopic gypsum crystals adhere. The microbes also influence crystal habit by (i) creating pores on the surfaces of gypsum crystals where smaller crystal precipitates form, and (ii) producing intercellular mucus in microbial mats, where suspended crystals can grow in all directions to produce polyterminal calcite crystals. Diatoms also mediate corrosion of the faces of calcite and gypsum crystals. Enriched δ13Cinorganicsignatures in the precipitates associated with microbial communities indicate that photosynthesis may promote precipitation of calcite and strontianite.

2007 ◽  
Vol 44 (6) ◽  
pp. 835-856 ◽  
Author(s):  
Sandy M Bonny ◽  
Brian Jones

The Flybye Springs, Northwest Territories, consist of 10 active vents and numerous small seeps that discharge sulphide- and barium-rich spring waters at an average temperature 8.5 °C. Oxidation of sulphide to sulphate drives precipitation of stellate and platy barite microcrystals in the proximal flow paths. Downstream, and in vent- and tributary-fed ponds, barite is precipitated among streamer and mat forming colonies of sulphur-tolerant microbes, including Thiothrix, Beggiatoa, Thioploca, Chromatium, Oscillatoria, fungi (dominantly Penicillium), and unicellular sulphate reducing bacteria. These microbes mediate barite saturation by adjusting redox gradients and via passive adsorption of barium ions to cell surfaces and extracellular polymeric substances. Passive biomineralization produces barite laminae in floating microbial mats, nanometric coatings, and micrometric encrustations around microbial cells and filaments, and local permineralization of Thiothrix, Beggiatoa, and Oscillatoria outer cell walls. Intracellular barium enrichment and (or) metabolic sulphur oxidation may be important to "active biomineralization" that produces nanometric barite globules on the tips of fungal hyphae, barite-filled cell cavities in Beggiatoa and Thiothrix, and baritized sulphur globules. Degradation of biomineralized cells generates detrital "microfossils," including barite tunnels, layered cylinders, solid cylindrical grains and chains of barite beads. The diversity of inorganic and biomineralized barite in the Flybye Springs flow path highlights the influence of ambient chemistry, microbial metabolism, and cellular structure on barite solubility and on the taphonomy of microfossils preserved in barite.


2012 ◽  
Vol 64 (1) ◽  
pp. 162-170 ◽  
Author(s):  
Kimberly A. Ross ◽  
Leah M. Feazel ◽  
Charles E. Robertson ◽  
Babu Z. Fathepure ◽  
Katherine E. Wright ◽  
...  

2006 ◽  
Vol 361 (1475) ◽  
pp. 1997-2008 ◽  
Author(s):  
David M Ward ◽  
Mary M Bateson ◽  
Michael J Ferris ◽  
Michael Kühl ◽  
Andrea Wieland ◽  
...  

We have investigated microbial mats of alkaline siliceous hot springs in Yellowstone National Park as natural model communities to learn how microbial populations group into species-like fundamental units. Here, we bring together empirical patterns of the distribution of molecular variation in predominant mat cyanobacterial populations, theory-based modelling of how to demarcate phylogenetic clusters that correspond to ecological species and the dynamic patterns of the physical and chemical microenvironments these populations inhabit and towards which they have evolved adaptations. We show that putative ecotypes predicted by the theory-based model correspond well with distribution patterns, suggesting populations with distinct ecologies, as expected of ecological species. Further, we show that increased molecular resolution enhances our ability to detect ecotypes in this way, though yet higher molecular resolution is probably needed to detect all ecotypes in this microbial community.


1974 ◽  
Author(s):  
M.S. Bedinger ◽  
F.J. Pearson ◽  
J.E. Reed ◽  
R.T. Sniegocki ◽  
C.G. Stone
Keyword(s):  

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