Lake Pavin History, geology, biogeochemistry, and sedimentology of a deep meromictic maar lake
295 tition for reducing equivalents less important (Dolfing 1999 ). From a thermodynamic point of view, dehalogenation via route ...
296 2e− → RHCln−1 + HCl and dichloroelimination by: RCln + 2H+ 2e− → RHCln−2 + 2HCl. Hydrogenolysis is the major degra- dation ...
297 substances as carbon and electron source. Over the past decades, many investigations focused on microbial degradation of aro ...
298 concentrations. These cytochromes have been proposed to mediate hexachloroethane, pentachloroethane and tetrachlo- romethane ...
299 Co-metabolism of Chlorinated Aliphatics Various chlorinated aliphatic compounds including VC, DCE and trichloroethene (TCE) ...
300 phototrophic anaerobe, Rhodospirillum photometricum. For chloroethenes and chlorinated aromatics, their mineraliza- tion int ...
301 the related prokaryotic actors are provided in Chap. 19. As described in the above paragraph, OHR generally occurs under met ...
302 Future works aiming at identifying Clorg present in Lake Pavin as well as characterizing microbial populations and enzymatic ...
303 Dolfing J (1999) Comment on “Methane as a product of chloroethene biodegradation under methanogenic conditions”. Environ Sci ...
304 Janssen DB, Pries F, van der Ploeg JR (1994) Genetics and biochemis- try of dehalogenating enzymes. Annu Rev Microbiol 48:16 ...
305 Neumann CS, Fujimori DG, Walsh CT (2008) Halogenation strategies in natural product biosynthesis. Chem Biol 15:99–109 Ni X, ...
306 Wagenknecht HA, Woggon WD (1997) Identification of intermediates in the catalytic cycle of chlororperoxidase. Chem Biol 4:36 ...
© Springer International Publishing Switzerland 2016 307 T. Sime-Ngando et al. (eds.), Lake Pavin, DOI 10.1007/978-3-319-39961-4 ...
308 estimated during a short-term study (Bettarel et al. 2003 ). Finally, we used small microcosms to access growth rates of pro ...
309 Mixotrophic oligotrichs ( Strombidium viride , Pelagohalteria viridis, Strobilidium caudatum, Strombidium sp1 ) largely domi ...
310 on the diatom Asterionella formosa. Katablepharis ovalis , bodonids, and small unifl agellated cells were not found to inges ...
311 ciliates was 4 × 10^6 bacteria L −1 h −1. Epilimnetic bacterivo- rous ciliates were dominated largely by small heterotrophic ...
312 18.6 Phagotrophic Ciliates as a Trophic Link Between Nanoplankton and Metazoa The in situ growth rates of the dominant plank ...
313 rates of small algivorous Urotricha spp. and autotrophic nano- fl agellates in all of the fractions studied, supporting the ...
314 potential and bacterial production in Lake Pavin: a short-term study. Microb Ecol 45:119–127 Bird DF, Kalff J (1986) Bacteri ...
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