Areas of marine geothermal
activity, such as hydrothermal vents provide a habitat rich in nutrients. This results
in hotspots of many species of organisms, and can account for some of the most
productive ecosystems on Earth. The depth at which these vents are formed far
exceed the reaches of light to aid photosynthetic processes, therefore the
organisms present at these vents rely on chemosynthesis. Chemoautotrophic micro
organisms account for the primary production, forming the base of many food
webs at these vent systems. The chemoautotrophs derive their nutrients from sulphur, iron or
magnesium, which are often products from the vent processes. They can be
present as microbial mats, symbiotes, free living, or they can be found in the
tubes of the vents themselves.
The hydrothermal vents
of Loihi seamount, located 21 miles East of Hawaii were used in this study.
Loihi seamount is seismically active, and the youngest of the island arc
formations of the Hawaiian Islands. The original vents which were discovered there
were named Pele’s Vents. They showed high concentrations of dissolved carbon
dioxide resulting in the low pH of 4.2. Fe(II) concentrations were
also high (a magnitude of 6 times higher than that of the surrounding water),
but the dissolved oxygen, magnesium and sulphate were depleted.
Following an eruption in 1996, Pele’s Vents
became extinct and Pele’s Pit, a caldera, took its place (a caldera is a crater
formed from the collapse of a volcano once the magma chambers below can no
longer support its weight). The vents in this caldera and in the areas
surrounding it (Naha and Ula Nui Vents) were the sites used in this study
(figure 1). Depths of the vents varied from 1116m to 4988m, and temperatures
ranged from 2°C to 165°C.
Figure 1: Map
of Pele’s Pit, and the locations where the microbial growth chambers were
deployed.
To conduct this study,
microbial growth chambers (MGCs) were constructed using plexiglass cylinders
which were enclosed at both ends to prevent the entry of macrofauna. The
interior of the cylinders were covered in a fine mesh of silica wool (8μm
diameter), which would be used as a substrate for micro organisms.
They were then deployed at seven sample sites (figure 1) using submersibles and
ROV’s, and kept there for short term (4-10 days) or long term periods (1-6
years). In total, 41 MGCs were deployed and recovered; 28 short term and 13 long
term over a ten year period. Once recovered, the MGCs were opened using aseptic
techniques, the silica wool was removed, placed into a sample bag, and frozen
immediately at -80°C until ready for processing. When necessary, the samples
were thawed on ice, the microbes present were isolated, DNA extraction took
place, and then a PCR was conducted to amplify the DNA.
All vent sites had
iron-rich microbial mats due to the Fe(II) enriched waters from the vents. The
cooler temperature vents were predominantly colonized by iron-oxidising ζ-proteobacteria,
and the warmer vents by sulphur-cycling ε-proteobacteria. Vents with an
intermediate temperature were colonized by both ε-proteobacteria and ζ-proteobacteria.
Therefore, the ε-proteobacteria and ζ-proteobacteria are the main colonisers of
the hydrothermal vents in the Loihu seamount, Hawaii.
I did enjoy reading
this paper, and it was the first to study and show that ζ-proteobacteria are
the dominant colonisers of low temperature hydrothermal vents. However, I
personally found that some of the methods used weren’t very well described, and
so I found it a bit difficult to interpret them into my own words.
Rassa, A. C.,
McAllister, S. M., Safran, S. A. & Moyer, C. L. (2009) Zeta-Proteobacteria dominate the colonization and formation of
microbial mats in low-temperature hydrothermal vents at Loihi Seamount, Hawaii.
Geomicrobiology Journal. 26: 623-638.
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