Methanogenesis In Environments Research Articles

Evidence of novel phylogenetic lineages of methanogenic archaea from hypersaline microbial mats.

Methanogenesis in hypersaline and high-sulfate environments is typically dominated by methylotrophic methanogens because sulfate reduction is thermodynamically favored over hydrogenotrophic methanogenesis in these environments. We characterized the community composition of methanogenic archaea in both unmanipulated and incubated microbial mats from different hypersaline environments in Baja California Sur, Mexico. Clone libraries of methyl coenzyme-M reductase (mcrA) sequences and DGGE band patterns of 16S rRNA and mcrA sequences showed that the methanogen community in these microbial mats is dominated by methylotrophic methanogens of the genus Methanohalophilus. However, phylogenetic analyses of mcrA sequences from these mats also revealed two new lineages corresponding to putative hydrogenotrophic methanogens related with the strictly hydrogenotrophic order Methanomicrobiales. Stimulated methane production under decreased salinity and sulfate concentrations also suggested the presence of hydrogenotrophic methanogens in these samples. The relative abundance of mcrA gene and transcripts, estimated by SYBR green I qPCR assays, suggested the activity of different phylogenetic groups of methanogens, including the two novel clusters, in unmanipulated samples of hypersaline microbial mats. Using geochemical and molecular approaches, we show that substrate limitation and values of salinity and sulfate higher than 3 % and 25 mM (respectively) are potential environmental constraints for methanogenesis in these environments. Microcosm experiments with modifications of salinity and sulfate concentrations and TMA addition showed that upper salt and sulfate concentrations for occurrence of methylotrophic methanogenesis were 28 % and 263 mM, respectively. This study provides phylogenetic information about uncultivated and undescribed methanogenic archaea from hypersaline environments.

Dolomitization of Holocene Shallow-Marine Deposits Mediated by Sulfate Reduction and Methanogenesis in Normal-Salinity Seawater, Northern Belize

ABSTRACT Dolomite constitutes an average of 12% of the Holocene organic-rich sediments over a 15 km2 area of the Cangrejo Shoals mudbank in northern Belize. Although it defines a laterally persistent stratiform body that averages 3 m thick, it is present throughout the 7.6-m-thick sediment section. These transgressive sediments are less than 6400 years old and were deposited in shallow-marine environments of normal salinity. The dolomite is dominantly cement, and average crystal size is 7 m. There are no significant correlations among amount of dolomite vs. sediment texture, mineralogy, porosity, or mole % MgCO3 in associated particulate high-Mg calcite, depth, or location on the shoals. The dolomites are poorly ordered and calcic (39.5-44.5 mole % MgCO3), with low mean Mn (210 ppm) and relatively high mean Sr (1034 ppm) concentrations. There is no evidence of recrystallization or geochemical alteration of the dolomite. 18O values of the dolomites range from 0.5 to 2.8o/ooPDB, and the mean value (2.1o/oo) suggests that the dolomite precipitated from normal-salinity pore water. Dolomite 13C values range from -5.2o/oo to +11.6o/ooPDB (mean seawater 13C = 0.5o/oo), which suggests dolomitization promoted by both bacterial sulfate reduction and methanogenesis in environments with anoxic pore water. Dolomitization attending these organodiagenetic reactions apparently was reversible over time, and episodic rather than continual precipitation is indicated. Requisite Mg and Ca were provided by seawater and by some dissolution of host sediments. The most rapid period of dolomitization may have been during early transgression, when relatively high sedimentation rates sustained high levels of organodiagenesis and pore-water alkalinities.