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Ninth international conference on - Marum

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104<br />

Abstracts of posters<br />

Comparis<strong>on</strong> of microbial communities in sub-surface sediments from Haak<strong>on</strong> Mosby mud<br />

volcano and a n<strong>on</strong>-seep site in the Barents Sea<br />

A. G. Rike 1 , E. Eribe 1 , E. Roinaas 2 , R. Orr 3 , K. S. Jakobsen 3 , T. Kristensen 2<br />

1 Norwegian Geotechnical Institute, P.O.Box 3930 Ullevaal Stadi<strong>on</strong>, NO-0806 Oslo, Norway<br />

2 Department of Moleculear Biosciences, University of Oslo, Norway<br />

3 Centre for Ecological and Evoluti<strong>on</strong>ary Synthesis (CEES), Department of Biology, University of Oslo, Norway<br />

The archaeal and bacterial diversity in sub-surface sediments at the Haak<strong>on</strong> Mosby Mud Volcano (HMMV) site,<br />

located at 72.0020 o N – 14.4350 o E, and at a n<strong>on</strong>-seep site (NSS) west of HMMV, at 72.0030 o N – 14.3700 o E, in<br />

the Barents Sea was studied. Both sampling sites are located at about 1300 m water depth. HMMV has been<br />

investigated by both geologists and biologists, and the microbial communities at different habitats have been<br />

described (Lösekann et al 2007, Niemann et al 2006). To the best of our knowledge, the microbial diversity in<br />

sediments not influenced by seeps in this regi<strong>on</strong> has not been characterized, and we were interested in studying<br />

the differences of these two microbial habitats.<br />

The bacterial and archaeal diversity at the sites was determined in sediments from 2-20 cm depth by 16S<br />

ribosomal DNA (16S rDNA) sequence analysis. DNA isolated from the sediments was PCR amplified, with<br />

universal-bacterial and -archaeal primers, and cl<strong>on</strong>ed into Escherichia coli. Sequences of approximately 900<br />

bases of cl<strong>on</strong>ed 16S rDNA inserts were used to determine species identity, or closest relatives, by comparis<strong>on</strong><br />

with sequences of known species. Geochemical parameters of sediments and pore water were determined to<br />

provide an envir<strong>on</strong>mental c<strong>on</strong>text of the sediment c<strong>on</strong>diti<strong>on</strong>s.<br />

Altogether, 245 microbial cl<strong>on</strong>es (from archaea and bacteria) were sequenced from the two sites, 152 from<br />

HMMV and 93 from the NSS. Archaeal cl<strong>on</strong>es represented 36% of total cl<strong>on</strong>es at HMMV and 26% at NSS.<br />

All 79 archaeal cl<strong>on</strong>es sequenced were detected as novel and their sequences were organized into tree clusters of<br />

Chrenarchaeota (A, B and C) and two clusters of Euryarchaeota (D and E).<br />

The 55 archaeal cl<strong>on</strong>es retrieved from HMMV represent 13 different phylotypes, all bel<strong>on</strong>ging to the<br />

Euryarchaeota clade E of anaerobic methane oxidizing archaea (ANME). The phylotypes are affiliated with<br />

clusters of ANME-2A, ANME-2B, ANME-2C and ANME-3. No Crenarchaeota were detected in the HMMV<br />

sediment investigated in this study. With the excepti<strong>on</strong> of two cl<strong>on</strong>es closely related to uncultured<br />

Thermoplasmatales in the Euryarchaeota phylum, the other 22 cl<strong>on</strong>es from the NSS sample affiliated to the<br />

Chrenarchaeota phylum. 63% of the NSS achaeal cl<strong>on</strong>es were close relatives of uncultured Desulfurococcus.<br />

166 bacterial cl<strong>on</strong>es, 97 from HMMV and 69 from the NSS were sequenced. Uncultured Epsil<strong>on</strong>proteobacteria<br />

accounted for 49% of the total bacterial cl<strong>on</strong>es in the HMMV sediments. Other main bacterial phyla detected at<br />

HMMV were Deltaproteobacteria (12%) and Gammaproteobacteria (10%). At the NSS the dominating phyla<br />

were Planctomycetes (25% ), Alphaproteobacteria (23%) and Obsidian Pool 11 (OP11) (14%). Out of 17<br />

bacterial phyla <strong>on</strong>ly 4 (OP11 group, Chloroflexi I/II, Gammaproteobacteria I/II and Deltaproteobacteria I/II)<br />

were comm<strong>on</strong> to both sites but any cl<strong>on</strong>es were detected at both HMMV and the NSS.<br />

The archaeal diversity in the anaerobic methane and hydrocarb<strong>on</strong> influenced HMMV sediments was<br />

significantly lower than in the aerobic deep cold sediments from the NSS. The bacterial diversity, however, was<br />

great at both sites. This may indicate that the archaeal comp<strong>on</strong>ent of the microbial community is most suceptible<br />

to seep influence than the bacterial comp<strong>on</strong>ent.<br />

Microbial methane cycle in the Black Sea sediments and its effect <strong>on</strong> the atmosphere<br />

and water column<br />

I. Rusanov 1 , N. Pimenov 1 , S. Yusupov 1 , and M. Ivanov 1<br />

1 Winogradsky Institute of Microbiology, RAS<br />

Methane is am<strong>on</strong>g the major terminal products of anaerobic organic matter (OM) transformati<strong>on</strong>, c<strong>on</strong>tributing to<br />

the atmospheric pool of greenhouse gases. During the period of 1990–2007, a unified procedure was applied to<br />

the radioisotope investigati<strong>on</strong> of microbial methane producti<strong>on</strong> and oxidati<strong>on</strong>, with short-term incubati<strong>on</strong> under<br />

in situ c<strong>on</strong>diti<strong>on</strong>s.<br />

The Black Sea area includes the following characteristic biogeochemical z<strong>on</strong>es:<br />

(1)sediments of the highly productive shallow coastal z<strong>on</strong>e, river estuaries, and river alluvial deposits; (2)<br />

extensive areas of shelf sediments, depths over 40–50 m; (3) sediments of the c<strong>on</strong>tinental slope and deep basins,<br />

permanently covered with anaerobic water; and (4) sediments of the methane seeps and mud volcanoes.<br />

Methane levels of the upper 30–50 cm of the sediments from the Dnepr and Dnestr estuarine coastal z<strong>on</strong>e, of the<br />

Danube delta and prodelta, and of the coastal shallow shelf stati<strong>on</strong>s were rather high for marine sediments.<br />

Methane c<strong>on</strong>centrati<strong>on</strong> increased sharply from 0.01–0.5 ml/dm 3 at the surface sediments to 0.1–66.0 ml/dm 3 at<br />

the depth 25–30 cm. This distributi<strong>on</strong> is caused by extensive microbial methane producti<strong>on</strong> (up to tens of µl/dm 3<br />

per day) in the upper 50 cm of the sediment and methane migrati<strong>on</strong> from the deeper sediment horiz<strong>on</strong>s. The

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