Exemplar Abstract for Gallionella ferruginea Ehrenberg 1838 (Approved Lists 1980).

2003 ◽  
Author(s):  
Charles Thomas Parker ◽  
Kara Mannor ◽  
George M Garrity
2003 ◽  
Author(s):  
Charles Thomas Parker ◽  
Dorothea Taylor ◽  
George M Garrity

Author(s):  
Evelyn Krawczyk-Bärsch ◽  
Andreas C. Scheinost ◽  
André Rossberg ◽  
Katharina Müller ◽  
Frank Bok ◽  
...  

2011 ◽  
Vol 77 (21) ◽  
pp. 7873-7875 ◽  
Author(s):  
Tomoko Suzuki ◽  
Hideki Hashimoto ◽  
Hiromichi Ishihara ◽  
Tomonari Kasai ◽  
Hitoshi Kunoh ◽  
...  

ABSTRACTThe structural and spatial associations of Fe with O and C in the outer coat fibers of theLeptothrix ochraceasheath were shown to be substantially similar to the stalk fibers ofGallionella ferruginea, i.e., a central C core, probably of bacterial origin, and aquatic Fe interacting with O at the surface of the core.


2012 ◽  
Vol 27 (3) ◽  
pp. 338-341 ◽  
Author(s):  
Tomoko Suzuki ◽  
Hideki Hashimoto ◽  
Hiromichi Ishihara ◽  
Nobuyuki Matsumoto ◽  
Hitoshi Kunoh ◽  
...  

Author(s):  
Evelyn Krawczyk-Bärsch ◽  
Andreas C. Scheinost ◽  
André Rossberg ◽  
Katharina Müller ◽  
Frank Bok ◽  
...  

1968 ◽  
Vol 14 (4) ◽  
pp. 385-389 ◽  
Author(s):  
Jay W. Nunley ◽  
Noel R. Krieg

In seven out of ten separate trials, contaminants in cultures of Gallionella ferruginea were eliminated by incubation of the crude culture for 1–2 days in Wolfe's medium containing 0.5% formalin. Purity was judged microscopically and also by the absence of contaminant growth in a variety of heterotrophic and autotrophic test media. Parallel cultures not treated with formalin exhibited growth of contaminants in most test media. Pure cultures of G. ferruginea have been maintained by serial transfer for at least 14 months and in continuous flow culture for at least 3 months. Preservation has been possible by storage at −80 °C in 15% glycerol. G. ferruginea in impure culture grew as a microaerophilic band closer to the surface of the fluid in the culture bottles than it did in pure culture; in the pure culture state it grew in a dense mat on the surface of the submerged ferrous sulfide agar. This difference probably resulted from the absence of oxygen-utilizing contaminants in the pure state.


2003 ◽  
Vol 807 ◽  
Author(s):  
Craig R. Anderson ◽  
Karsten Pedersen

ABSTRACTBiofilms were grown in situ 296 metres below sea level in the Äspö Hard Rock Laboratory. The prominent organism in these biofilms wasGallionella ferruginea, which is an iron oxidising chemolithotrophic microorganism that grows in low oxygen conditions. This organism grows an organic stalk structure capable of binding and concentrating trace metals. This stalk structure also allows amorphous ferric iron oxyhydroxides, or BIOS, (bacteriogenic iron oxides) to precipitate. The pH of the groundwater within the system was between 7.4 and 7.6, with Eh potential between 150 and 190 mV and oxygen saturation between 3 and 15%. Biofilms developed within two weeks and were sampled every two weeks for three months. Cell number and stalk length was recorded for each sample. The concentration of Cr, Ni, Cu, Zn, Mo, REE (rare earth elements), U-238 and Th-232 was measured by ICP-MS. Early results suggested thatGallionellabiofilms and associated BIOS could potentially concentrate trace metals up to 1000 fold higher than levels within the host rock and over 1 000 000 times the levels in the groundwater over a period of years. These new experiments indicate thatGallionellabiofilms and BIOS can rapidly attenuate metals to levels over 1000 fold higher than the levels in the groundwater. This process can occur anywhere where reduced groundwater enters the waste repository tunnel, open cavities or where groundwater extrudes at the surface. Because of this, there is huge potential to use biofilms and BIOS for retention of radionuclides and pollution control.


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