Lake Pavin History, geology, biogeochemistry, and sedimentology of a deep meromictic maar lake
275 collected in strata where an optimal activity of methanotro- phy was observed. A wide range of growing conditions was achiev ...
276 AOM coupled to denitrification CH 4 oxidation coupled to denitrification was first demon- strated in an anaerobic enrichme ...
277 Enrichment cultures consisted of 10 % archaea of the order Methanosarcinales distantly related to ANME-2, named ANME-2d, the ...
278 for the growth of microorganisms performing AOM: anoxia, availability of CH 4 and of alternative electron acceptors other th ...
279 the superficial sediments and in the dysoxic and anoxic waters of Lake Pavin are bacterial C 16 fatty acids and hopanoids (d ...
280 Bapteste E, Brochier C, Boucher Y (2005) Higher-level classification of the Archaea: evolution of methanogenesis and methano ...
281 genic archaeon isolated from human faeces. Int J Syst Evol Mirobiol 62:1902–1907 Dubrunfault M (1856) Note sur la chaleur et ...
282 Knittel K, Boetius A (2009) The anaerobic oxidation of methane- progress with an unknown process. Annu Rev Microbiol 63:311– ...
283 Nüsslein B, Eckert W, Conrad R (2003) Stable isotope biogeochemistry of methane formation in profundal sediments of Lake Kin ...
284 Von Stockar U, Marison IW (1989) The use of calorimetry in biotech- nology. In: Fiechter A (ed) Advances in biochemical engi ...
© Springer International Publishing Switzerland 2016 285 T. Sime-Ngando et al. (eds.), Lake Pavin, DOI 10.1007/978-3-319-39961-4 ...
286 osmoregulation of cells (White and Broadley 2001 ), and is an important electrolyte for regulation of muscle function and sy ...
287 Gustavsson et al. 2012 ). Thus, a large proportion of Cl− deposited in terrestrial ecosystems can be transformed into Clorg ...
288 17.2.2 Processes of OM Chlorination Oceans, with a water volume of about 1.36 × 10^8 km^3 and a Cl content of approximately ...
289 (DCA) or also carbon tetrachloride can be released (Gribble 2004 ). Some human activities can also accelerate these natu- ra ...
290 lignocellulose in order to access carbon, a limited resource in some environments, (ii) to dissolve cell wall for cell penet ...
291 They may catalyze the synthesis of chlorinated antibiotics in bacteria (Bernhardt et al. 2011 ). V-CPOs seem to be exclusive ...
292 media (Fig. 17.5) (Kirk and Conrad 1999 ). The peroxyacids oxidize Cl− to OCl−, which then halogenates organic sub- strates ...
293 enzyme effects chlorination rather than hydroxylation of unactivated methyl groups in substrates (Fujimori and Walsh 2007 ; ...
294 totally different reaction mechanisms, under aerobic or anaerobic conditions (Janssen et al. 2001 ; de Jong and Dijkstra 200 ...
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