The gabbroic microbial
community resulted to be relatively depauperate, consisting of a low
diversity of proteobacterial lineages closely related to known
hydrocarbon degraders, while little or no evidence of Archaea in
either rock or seawater samples was found by the authors, despite
their numerous attempts to amplify archaeal 16S rRNA genes.
Prokaryotic cell densities of interior sections of core samples over
the entire 1400 m interval were below the level of detection (<103
cells cm-3) and much lower than those normally reported
for basalts and carbonates in other studies. These low cell densities
were congruent with the low species diversity obtained by the authors
with DGGE and T-RFLP analysis. Microbial diversity however, was found
to vary with depth from 400–1400 mbsf and interestingly, this depth
variance was related to rock alteration, with the most altered rock
supporting the greatest microbial diversity. Probably because
alteration could result in changing permeability and oxidation state
of the rocks, providing thus, additional niches in the gabbroic
rocks.
Subsequently, in order to
provide insight into the potential metabolic diversity of the
microbial community, the authors analyzed conserved regions of
functional genes using a 'GeoChip' microarray. Results revealed that
genes coding for hydrocarbon degradation (methane and toluene
oxidation) and anaerobic respirations (nitrate, sulfate and iron
reduction) were present in rock samples, as well as genes for carbon
and nitrogen fixation, denitrification, ammonium-oxidation, organic
contaminant degradation and metal toxicity/resistance. The
predominant genes were found to code for organic contaminant
degradation, carbon degradation, carbon fixation, methane oxidation and
methane generation. For all these reasons, the authors suggested that
the gabbroic layer hosts a complex microbial community able to
degrade hydrocarbons, fix carbon and nitrogen and employ various
non-oxygen electron acceptors in both aerobic and anaerobic
conditions.
In this case, the presence of seawater circulation
processes in the upper 800 meters of oceanic crust, would provide the
limited amount of oxygen required for aerobic processes, with a
transition to anaerobic processes following oxygen depletion below
800 mbsf, where reducing conditions tend to prevail.
Since, marine basalts and
gabbros are nearly identical in chemical composition, the authors
initially hypothesized that similar organisms specialized for growth
in subsurface igneous rocks would have been recovered also from
gabbros. However, none of the clades endemic to basalts were found in
gabbros and the high similarity of gabbroic microorganisms to
hydrocarbon degrading bacteria, suggested instead, that gabbroic
microflora are not ocean crust endemic specialists, but rather they
are transient generalist microbes, able to survive in a variety of
hydrocarbon-rich environments, including deep subsurface igneous
rocks, such as those analyzed in this study. Abiotic production of
unbranched alkanes (including methane) through serpentinization
reactions in the Earth’s crust was suggested by the authors,
raising the intriguing possibility that these deep hydrocarbons could
provide carbon and energy to extant microbial communities and support
complex micro-endolithic populations in the interior of the oceanic
crust. In conclusion, since ocean crust covers 70% of the earth’s
surface, endolithic microbial processes in this subseafloor
environment, do really have the potential to significantly influence
oceanic and atmospheric biogeochemistry and so, future efforts should
be directed towards quantifying the role and the importance of these
processes on a global scale.
Reference:
Mason O. U., Di Meo-Savoie
C., Van Nostrand J. D., Zhou J., Fisk M. R., Giovannoni S. J. (2010).
First investigation of the microbiology of the deepest layer of ocean
crust. PLoS ONE5, e15399.
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