Present Address: Thomas Pape, Research Center Ocean Margins, University of Bremen, PO Box 330440, D-28334 Bremen, Germany.
The influence of ultramafic rocks on microbial communities at the Logatchev hydrothermal field, located 15°N on the Mid-Atlantic Ridge
Article first published online: 16 MAY 2007
FEMS Microbiology Ecology
Volume 61, Issue 1, pages 97–109, July 2007
How to Cite
Perner, M., Kuever, J., Seifert, R., Pape, T., Koschinsky, A., Schmidt, K., Strauss, H. and Imhoff, J. F. (2007), The influence of ultramafic rocks on microbial communities at the Logatchev hydrothermal field, located 15°N on the Mid-Atlantic Ridge. FEMS Microbiology Ecology, 61: 97–109. doi: 10.1111/j.1574-6941.2007.00325.x
Editor: Gary King
- Issue published online: 16 MAY 2007
- Article first published online: 16 MAY 2007
- Received 7 September 2006; revised 18 February 2007; accepted 27 February 2007.First published online 16 May 2007.
- Logatchev hydrothermal field;
The ultramafic-hosted Logatchev hydrothermal field (LHF) on the Mid-Atlantic Ridge is characterized by high hydrogen and methane contents in the subseafloor, which support a specialized microbial community of phylogenetically diverse, hydrogen-oxidizing chemolithoautotrophs. We compared the prokaryotic communities of three sites located in the LHF and encountered a predominance of archaeal sequences affiliated with methanogenic Methanococcales at all three. However, the bacterial composition varied in accordance with differences in fluid chemistry between the three sites investigated. An increase in hydrogen seemed to coincide with the diversification of hydrogen-oxidizing bacteria. This might indicate that the host rock indirectly selects this specific group of bacteria. However, next to hydrogen availability further factors are evident (e.g. mixing of hot reduced hydrothermal fluids with cold oxygenated seawater), which have a significant impact on the distribution of microorganisms.
Deep-sea hydrothermal environments contain a variety of biotopes which are characterized by steep physical and chemical gradients (Kelley et al., 2002). The physico-chemical conditions which provide the essentials for microbial life include pH, temperature, oxygen levels and energy sources, e.g. hydrogen, sulfur and methane (Kelley et al., 2002). The most important physiological group of microorganisms is the chemolithoautotrophs. They are responsible for the local microbial primary production.
Both basalt- and ultramafic-hosted hydrothermal systems are found in Mid-Ocean Ridge spreading areas. The type of host rock determines the chemical composition of the fluids emitted from the vent systems. In turn, these fluid emissions supply the indigenous prokaryotes with the energy and carbon sources necessary to fuel primary production. The fluids found in ultramafic-hosted systems reveal significantly higher concentrations of hydrogen than those which occur in basalt-hosted systems (Wetzel & Shock, 2000).
Several studies are available on the microbial diversity of geographically distinct basalt-hosted systems. In contrast, only three (including the present study) have concerned themselves with ultramafic-hosted hydrothermal environments (the Lost City, Rainbow and Logatchev hydrothermal fields; for references see Table 1). Generally, the chemolithoautotrophic communities of hydrothermal environments show a clear predominance of only a few phylogenetic lineages. These include representatives of Methanococcales, Epsilonproteobacteria or Aquificales (e.g. Huber et al., 2002, 2003; Takai et al., 2003, 2004a; Nakagawa et al., 2005a).
|Mid-Ocean Ridge||EPR||CIR||Rainbow§||MAR||Lost City∥|
|Hydrothermal vent field||NT†||Edmond‡||Logatchev¶|
|Vent site of microbiological sample||Near Bio 9||Fuzzy toothpick||Irina II||Irina I||Site B||Atlantis massif|
|H2S (μmol kg−1)||≤3.300*||ND||≤2.500||116||277||1.241||64*|
|H2 (mmol kg−1)||≤0.3*||0.2*||13.0*||2.2||5.9||1.8||≤14|
|CH4 (mmol kg−1)||≤0.015*||0.4*||2.2*||0.7||1.5||0.6||≤2|
|Methanosarcinales ANME Group||−||−||ND||−||−||+||+|
Members of the archaeal order Methanococcales are strictly anaerobic and use hydrogen and carbon dioxide as a substrate for methanogenesis (Whitman et al., 1992). They have been associated with the subvent biosphere (Huber et al., 2002; Nakagawa et al., 2005a), where they are probably among the most important primary producers (Huber et al., 2002). Within the bacterial domain many affiliates of the Epsilonproteobacteria have been described as autotrophs (Campbell et al., 2006). They might also play a considerable part in primary production in vent environments. Their ability to utilize a wide range of electron donors and electron acceptors (e.g. hydrogen, sulfur compounds, nitrate and oxygen) suggests their importance in hydrogen, sulfur and nitrogen cycling in hydrothermal biotopes (Takai et al., 2003; Nakagawa et al., 2005b; Campbell et al., 2006). Epsilonproteobacterial representatives have been classified into at least six subgroups, known as A, B, C, D, F and G (Corre et al., 2001). However, it recently came to light that the group C sequences had been misclassified (Campbell et al., 2006). Other chemolithotrophic bacteria involved in hydrogen oxidation include thermophiles of deeply rooted lineages e.g. Persephonella spp. or Desulfurobacterium spp. (L'Haridon et al., 1998; Götz et al., 2002). Additionally, sulfur-oxidizing mesophiles such as Thiomicrospira spp. have been encountered in hydrothermal emissions (Jannasch et al., 1985; Takai et al., 2004b).
This is the first assessment of microorganisms inhabiting the Logatchev hydrothermal field (LHF). The aim of this study was to evaluate the microbial communities present in hydrothermal vent emissions at three sites and to identify possible shifts in community composition linked to changes in the chemistry of the hydrothermal fluids. Ultramafic-hosted hydrothermal systems possibly represent our closest analogue to early earth environments (Holm & Charlou, 2001). They could have played a role in the origin and evolution of life (Shock & Schulte, 1998). It is therefore vital that we expand our understanding of the interplay between source rock, fluid chemistry and the microbial populations in ultramafic-hosted hydrothermal systems such as the LHF.
Materials and methods
Site description, sample collection and fluid characteristics
Hydrothermal fluid samples were retrieved during dives made by the remotely operated vehicle (ROV) QUEST (MARUM, University of Bremen) during the HYDROMAR I (M60/3, 2004) and HYDROMAR II (M64/2, 2005) cruises to the LHF. The LHF is located at 14°45′N and 44°58′W on the northern Mid-Atlantic Ridge (MAR) in water depths of between 2960 and 3060 m (Bogdanov et al., 1997; Kuhn et al., 2004). High-temperature fluid emissions were collected from two smoking craters (Irina I and Site B) and the chimney structure at Irina II, which are all located within an area of 0.04 km2.
The samples were retrieved using a pumped flow-through system (Kiel Pumping System KIPS) specially designed for the ROV QUEST (Garbe-Schönberg et al., 2006). To minimize microbial cross-contamination between the ambient seawater and the hydrothermal fluids the nozzle of the KIPS was placed into the hot vent orifice before collection of the samples. To ensure a complete exchange of fluids while samples were being taken, pumping continued for c. 1 h. Fluid chemical analysis and microbial diversity studies were conducted using hydrothermal liquids from aliquots of the same sample. Once on board the ship, the liquids intended for microbiological studies were concentrated on 0.2-μm pore size polycarbonate filters (Sartorius) and stored at −20°C.
While exit temperatures of 300–350°C were measured in fluid emissions from the smoking crater sites temperatures recorded for fluid outflow at the main chimney complex (Irina II) were lower (170°C) (Table 1) (Lackschewitz et al., 2005). The LHF ultramafic-hosted hydrothermal system shows distinct differences in rock mineralogy (Kuhn et al., 2004). The reaction of heated seawater with gabbroic rocks is indicated. Serpentinization processes, caused by ultramafic rock-water interactions, are responsible for extremely high hydrogen (≤19 mM) and methane (≤3.5 mM) concentrations in the hydrothermal fluids, while sulfide concentrations do not exceed 3.5 mM (Schmidt et al., 2007).
Analysis of fluid chemical parameters
The pH and sulfide concentrations were determined immediately after sample recovery. The pH was measured (Mettler electrodes with Ag/AgCl reference electrode) at 25°C in unfiltered sample aliquots. Sulfide concentrations were determined photometrically following the methylene blue method (Cline, 1969) or, for samples with low concentrations, by voltammetry (Metrohm Application Bulletin 199/3e). Methane was analyzed on board by applying a purge and trap technique (Seifert et al., 1999). In order to determine the δ13C of methane, the water samples were degassed into a high-grade vacuum. Aliquots of the released gas were stored in gastight glass ampoules for later on-shore analysis by GC-Isotope-Ratio-Mass-Spectrometry (Seifert et al., 2006). For on-board measurements of dissolved hydrogen the water sample was degassed into a high-grade vacuum. Aliquots of the released gas were analyzed by gas chromatography (Thermo Electron Corporation Trace GC Ultra, column: packed stainless steel (Molecular sieve 5 Å), oven temperature: isotherm 40°C, carrier gas: He, detection: pulsed discharge detector). Analytical procedures were calibrated daily with standard commercial gas (LINDE). Extrapolation of the sample concentrations to end-member concentration was carried out on the assumption that the hydrothermal end-member fluids do not contain dissolved magnesium (Mg=0) (Mottl & Holland, 1978). All presented values are end-member concentrations.
DNA extraction, 16S rRNA gene amplification, cloning and sequencing
DNA was extracted from filters using the Ultra Clean Soil DNA Isolation Kit (MoBio) according to the manufacturer's instructions. Archaeal and bacterial 16S rRNA genes were PCR-amplified using oligonucleotide primer sets consisting of 21F and 958R (DeLong, 1992) and 27F and 1492R (Lane, 1991), respectively. Primers (50 pmol μL−1), 1 μL (bacteria) and 1.5 μL (archaea) of DNA template, and sterile water were added to PuReTaq Ready-To-Go-PCR Beads (Amersham Biosciences) to a total volume of 25 μL. An initial denaturation step (92°C for 2 min) was followed by 20 cycles of 92°C for 40 s, 50°C for 40 s, 72°C for 1 min for bacteria and 94°C for 1 min, 58°C for 1 min and 72°C for 1 min for archaea. The final extension was 5 min at 72°C. To minimize PCR bias 20 cycles were conducted (Qiu et al., 2001). The amplified product was purified by the Roche PCR purification kit according to the manufacturer's instructions and reamplified as described above using 1 μL of the purified extracts. PCR products were repurified as mentioned previously and subcloned with a TOPO-TA cloning kit (Invitrogen, Carlsbad, CA). In order to screen for 16S rRNA genes, 100 clones for each site were randomly picked and then resuspended in 25 μL of sterile water. The clones were checked for correct insert size by PCR with the M13F and M13R vector primers. PCR products of the correct size (∼1500 bp) were screened and partially sequenced (∼500 bp) for bacteria or archaea with 27F or 21F, respectively. Sequencing was performed using the ABI PRISM® BigDye™ Terminator Ready Reaction Kit (Applied Biosystems) and an ABI PRISM® 310 Genetic Analyzer (Perkin Elmer Applied Biosystems). To clarify phylogenetic affiliation of specific bacterial sequences, full sequences were obtained using the primers 342F, 1492R (Lane, 1991), 534R (Muyzer et al., 1993) and 1094R (Munson et al., 1991).
Sequences were edited and assembled with Lasergene Software seqman (DNAStar Inc.). Chimeric sequences were identified using the chimera-check software available from Ribosomal Database Project (Cole et al., 2003) and then eliminated. Sequences were compared with DNA sequences in the public domain through blastn searches (Altschul et al., 1997). Sequence data was compiled using arb software (http://www.arb-home.de) and then aligned with sequences obtained from the GenBank database using the arb fastaligner utility (Ludwig et al., 2004). The resulting alignments were manually verified against known secondary structure regions. Maximum-likelihood-based trees were constructed using PhyML (Guindon & Gascuel, 2003). The phylip version 3.65 package (J. Felsenstein, University of Washington, Seattle) was used additionally to construct a maximum-parsimony tree (DNAPARS) for sequences of deeply rooted lineages. Bootstrap analysis (SEQBOOT) was used to provide confidence estimates for maximum parsimony tree topologies. All trees were constructed using 100 bootstrap replicates and near full-length sequences. The trees were imported into arb and shorter sequences added to trees using the Parsimony Quick and Add option.
End-member concentrations of the hydrothermal fluids emanating at the three vent sites (Irina I, Irina II and Site B) are summarized in Table 1. Both the pH measurements and sulfide concentrations of Irina I and Irina II were strongly affected by dilution of the hydrothermal sample with seawater prior to and during sampling (Mg>40 mM). The pH (25°C) for fluids at Irina I, Irina II and Site B were 6.2, 7.3 and 3.8, respectively (Table 1). Fluid samples taken at Irina I revealed the highest hydrogen and methane concentrations in this study (5.9 and 1.5 mM, respectively), but low sulfide contents (277 μM) (Table 1). The hydrogen and methane contents of fluid samples taken at Irina II amounted to 2.2 and 0.7 mM, respectively, and 116 μM of sulfide was found (Table 1). In contrast, at Site B, where the level of seawater dilution was lowest (50% end-member), the highest sulfide concentrations in this study were observed (1.2 mM). Hydrogen and methane contents accounted for 1.8 and 0.6 mM, respectively. Stable carbon isotope signatures were determined for methane and ranged between −9.3‰ and −13.9‰.
Three archaeal and bacterial clone libraries were constructed with samples originating from three vent sites in the ultramafic-hosted LHF. Fluid emissions from the chimney structure at Irina II and the smoking craters at Irina I and Site B yielded 65, 80 and 93 bacterial and 46, 35 and 34 archaeal sequences, respectively. Clone sequences with similarities of ≥97% were defined as an operational taxonomic unit (OTU).
Sequences retrieved from fluid emissions at the LHF, but which are generally found in the open water column (e.g. Acinas et al., 1999; Long & Azam, 2001; Bano & Hollibaugh, 2002), were not taken into consideration. Their presence was assumed to be caused by mixing with ambient seawater during collection of fluid samples, with the ultramafic setting of the LHF not being a significant selection factor. Bacterial sequences not considered for this reason amount to 73%, 30% and 32% of fluid emissions at Irina I, Irina II and Site B, respectively. These mainly include Gammaproteobacteria (e.g. Vibrionales, Alteromonadales, Oceanospirillales), Alphaproteobacteria (Rhodobacterales) and Bacteroidetes as well as very few Betaproteobacteria (Burkholderiales), Planctomycetales, Clostridia or Actinobacteria. Among archaea, 26%, 33% and 47% of sequences retrieved from fluids at Irina I, Irina II and Site B, respectively, were excluded from analyses for the same reason as that mentioned above. This includes a major faction affiliated to the Crenarchaeotic Marine Benthic Group I, which occurs at various locations. However, percentages of OTUs were calculated from the total number of all bacterial or archaeal clone sequences obtained per vent site.
A large part of the indigenous microbial community (bacteria and archaea) of the LHF was related to organisms known as autotrophic hydrogen-oxidizers. The limitations to inferring physiological properties from the analysis of 16S rRNA gene sequences have already been demonstrated (e.g. Kashefi et al., 2002). Nevertheless, in some instances, it may be possible to infer physiological traits of uncultured organisms from the physiology of very closely related microorganisms that are available in culture or from group-specific characteristics. For example, all cultured Epsilonproteobacteria affiliated to group D are capable of oxidizing hydrogen (for review see Campbell et al., 2006).
At Irina I, Irina II and Site B affiliates of the Epsilonproteobacteria constituted 19%, 45% and 49%, respectively, of all retrieved bacterial clone sequences. Phylogenetically diverse representatives of Epsilonproteobacteria were encountered in emissions at Irina I and Irina II (Fig. 1a). This included members of groups B, D, F and Sulfurospirillum spp. (Irina I) and affiliates of groups A, B, F and G (Irina II) (Fig. 1a). By contrast, Site B epsilonproteobacterial sequences were restricted to groups B and F (Fig. 1a).
At Irina II, representatives of group A comprised 9% of the clone sequences and were closely related (99%) to Hydrogenimonas thermophila (Fig. 1a). At Irina I only 6% of bacterial sequences were related to members of group F. In contrast, they contributed significantly to the clone libraries recovered from fluids at Irina II and Site B (31% and 47%, respectively). The majority of these sequences clustered into a deeply diverging group with no known cultured representatives (Fig. 1a). They were related exclusively to sequences originating from vent environments. The closest described isolate of these LHF sequences was Sulfurovum lithotrophicum (sequence similarities 86–98%). Only a minority of clone sequences at Irina I (6%), Irina II (3%) and Site B (1%) were associated with group B (Fig. 1a). Sequences affiliated to Sulfurospirillum spp. were restricted to Irina I (Fig. 1a).
Deeply rooted lineages
Sequences of deeply rooted lineages constituted a minor fraction of clones (Fig. 1b). At Irina I, 5% of the bacterial clone sequences were closely related to Desulfurobacterium sp. (99%), Persephonella sp. (98%) and Oceanithermus profundus (99%) (Fig. 1b).
A single sequence originating from fluids emitted at Irina I and 9% of sequences at Irina II were affiliated with sequences of the group C Epsilonproteobacteria, recently recognized as having been misclassified (Campbell et al., 2006). New tree calculations place them as a new group (RE1) in close proximity to the candidate division SR1 (Fig. 1b). High bootstrap values support this position in maximum likelihood and maximum parsimony tree topologies (Fig. 1b). The OTUs were related to sequences from different hydrothermal environments such as the Guaymas Basin (Dhillon et al., 2003), the East Pacific Rise (Alain et al., 2004) or the Mid-Atlantic Ridge (Corre et al., 2001) (Fig. 1b). Two sequences from Site B were grouped in the uncultured candidate divisions SR1 and OD1, which were only distantly related (94%) to their closest relatives (Fig. 1b).
At Irina II 8% of the bacterial sequences were identical to thioautotrophic and methylotrophic symbionts of Bathymodiolus spp. A single sequence at Irina I clustered with methylotrophic symbionts of these vent mussels. In contrast, at Site B no sequences were related to symbionts of Bathymodiolus spp. However, at this site two gammaproteobacterial sequences were found that resembled symbiont sequences of Escarpia spicata (Di Meo et al., 2000) and Codakia orbicularis (Gros et al., 1996).
Fluids at Irina II and Site B additionally included members of the Deltaproteobacteria (8% and 15%, respectively). They were exclusively associated with the Desulfobulbaceae family (Fig. 1c). The majority of fluid sequences at Irina II (5%) and at Site B (11%) were related to Desulfocapsa sulfexigens (Fig. 1c).
At the Irina I, Irina II and Site B vent locations, members of the order Methanococcales accounted for 74%, 68% and 50% of archaeal clone sequences, respectively (Fig. 1d). Only a few species of the Deep-Sea Hydrothermal Vent Euryarchotic Groups I and II, with no cultured representatives, were identified (data not shown).
Sequences related to “Methanococcus aeolicus” prevailed among the archaeal clone libraries at Irina I (43%), Irina II (54%) and Site B (47%) (Fig. 1d). Representatives related to Methanocaldococcus infernus were also present at Irina I (14%), at Irina II (4%) and at Site B (3%) (98–99% sequence similarities). Other methanogens found at Irina I (11%) include Methanothermococcus thermolithotrophicus (99% sequence similarity). At Irina II, 9% of the sequences were only distantly related (94%) to Methanocaldococcus janaschii. Additionally at Site B a single sequence was identified as a member of the ANME-2 lineage.
Our study was the first assessment of the microbial community inhabiting the LHF. The geological setting of the ultramafic-hosted field results in the release of high hydrogen concentrations within the emanated fluids (Table 1). Possibly, as a consequence, a large fraction of the microorganisms inhabiting the LHF was associated with hydrogen-oxidizers (Fig. 1a, b and d).
The archaeal community from all studied vent locations was very similar and detected archaea were mainly affiliated to Methanococcales (Fig. 1d). In contrast, the bacterial communities varied at the three locations studied. It seemed that an increase in hydrogen results in a diversification of potential hydrogen-oxidizing bacteria. Nonetheless, the microorganisms detected were associated with cultured prokaryotes differing in growth temperatures and tolerances towards oxygen. This strongly suggests the importance of mixing processes next to the abundance of available energy sources for the inhabitance of the hydrothermal biotopes.
The selection of ultramafic rocks for microorganisms
Methanococcales use hydrogen and CO2 as a substrate for hydrogenotrophic methanogenesis (Whitman et al., 1992). The prevalence of archaeal sequences associated with the Methanococcales at all investigated LHF sites (Fig. 1d) might indicate a selection for methanogenic archaea by the ultramafic-hosted system. Stable carbon isotope signatures determined for methane do not hint at a significant proportion of biogenic methane. This argues against the metabolic significance of Methanococcales in the LHF. Nevertheless, a biogenic methane signature might be masked due to a high background level of nonbiogenic methane.
Representatives of the Epsilonproteobacteria and of deeply rooted lineages have been associated with hydrogen oxidation (L'Haridon et al., 1998; Götz et al., 2002; Campbell et al., 2006). In contrast to the archaeal community, the fluids at each of the three vent emission sites support different bacterial communities (Fig. 1a–c). It seemed that an increase of hydrogen led to a more diverse community of putative hydrogen-oxidizing bacteria. For example, at Irina I, where the highest hydrogen concentrations were found in this study, potential hydrogen-oxidizing affiliates were distributed throughout the entire bacterial domain. These included Aquificales and Epsilonproteobacteria (group D) (Fig. 1a and b). At Irina II, where significantly lower hydrogen concentrations were found, less diverse potential hydrogen-oxidizing bacteria were present (Fig. 1a, Table 1). They were limited to the epsilon subdivision of the Proteobacteria (groups A and G). In contrast, at Site B, which had only slightly lower hydrogen contents than Irina II, no typical hydrogen-oxidizing bacteria were observed. The organisms detected here were affiliated to groups B and F (Fig. 1a). Only some associates of these groups have been shown to be capable of hydrogen oxidation, while others are able to utilize reduced sulfur compounds (Campbell et al., 2006). However, studies conducted on the NiFe-Uptake Hydrogenase (catalyzes the oxidation of molecular hydrogen), from fluids emitted at Irina II and Site B, demonstrated the potential of diverse Epsilonproteobacteria to be involved in hydrogen oxidation (M. Perner, unpublished data). The presence of putative hydrogen-oxidizers at all LHF locations might indicate that the ultramafic rock hosting the hydrothermal system selects for organisms with specific physiologies (hydrogen oxidation). If the nature of the host rock was the only factor influencing the distribution of the microorganisms, one would expect this to be reflected in diversity analyses obtained from other ultramafic-hosted systems. However, this is not the case (Table 1).
Out of all the active venting sites, the Rainbow vent field, with its geological setting and fluid-physico-chemistry, is the one most similar to the LHF (Donval et al., 1997; Lackschewitz et al., 2005). Nonetheless, in Rainbow hydrothermal environments hydrogen-oxidizers such as Aquificales or of members associated with e.g. groups A or D (Epsilonproteobacteria) were not detected (López-García et al., 2003) (Table 1). However, the three LHF locations have shown that bacterial diversity can differ significantly even though general chemical parameters seem to be similar (Table 1). In contrast, Methanococcales were found at the Rainbow field using functional gene analysis (Nercessian et al., 2005). This is in agreement with archaeal communities observed in the LHF emissions (Fig. 1d). Although the Lost City vent field is ultramafic-hosted and fluids have high hydrogen concentrations, the physico-chemical features of the emitting fluids are very different to those found in the LHF and the Rainbow field (for references see Table 1). The role of methane as a microbial energy source seems to be pronounced in the Lost City environment (Brazelton et al., 2006). Again, however, even though high hydrogen contents were ascertained, no typical hydrogen-oxidizing organisms were apparent (Brazelton et al., 2006). However, hydrogen oxidation has been suggested for some prokaryotes (Brazelton et al., 2006).
In contrast to the ultramafic-hosted systems described above, basalt-hosted hydrothermal systems typically reveal lower hydrogen contents (e.g. Van Dover et al., 2001; Von Damm & Lilley, 2004). Despite the low hydrogen concentrations of these basalt-hosted environments, microbial communities consisted in part of organisms related to phylogenetically diverse hydrogen-oxidizing microorganisms (e.g. Hoek et al., 2003; Kormas et al., 2006) (Table 1). As microorganisms detected at Site B show, relatively high concentrations of hydrogen do not necessarily result in phylogenetically diverse hydrogen-oxidizing communities. This set of findings indicates the importance of several other parameters essential in controlling the composition of the microbial population. The large number of phylogenetically diverse species affiliated with organisms characterized by various temperature and oxygen requirements suggests that mixing processes (hydrothermal fluids and oxygenated seawater) play an important role for the microbial community.
The importance of mixing processes
Our frequent encounters of bacteria and archaea related to cultured representatives with different temperature and oxygen requirements suggests mixing processes at the three vent locations. As hydrothermal fluids rise to the surface they mix with ambient seawater and cause physico-chemical gradients. These physico-chemical features are reflected in the physiologies of organisms adapted to these environments. Therefore the detection of specific groups can give an indication of the intensity of these mixing processes. The highest phylogenetic diversity throughout the bacterial domain was observed at Irina I. It included members of Epsilonproteobacteria and deeply rooted lineages (Fig. 1a and b). A thermophilic lifestyle is a group-specific characteristic of some of these representatives (L'Haridon et al., 1998; Götz et al., 2002; Campbell et al., 2006). Again, in emissions from Irina II, organisms were detected which were linked to thermophilic Epsilonproteobacteria. However, these Epsilonproteobacteria are characterized by slightly lower growth temperatures compared to cultured members of the deeply rooted lineages found at Irina I but absent from Irina II. This implies that the habitable environments at Irina I allow less intense mixing processes than the biotopes at Irina II. At Site B, no prokaryotes were observed related to thermophilic bacteria. The only microorganisms typically known for a thermophilic lifestyle included archaea of the order Methanococcales (Fig. 1d). Epsilonproteobacteria inhabiting Site B biotopes were exclusively affiliated to members of groups B and F. Their cultured representatives have been described as mesophiles (for review see Campbell et al., 2006). This could indicate that bacterial life at this location is only possible in environments where dilution of the hydrothermal fluids is ensured.
The presence of chemical gradients observed is also reflected in different levels of oxygen requirements characteristic for certain cultivated groups. As shown, several organisms at Irina I were related to bacteria with a thermophilic lifestyle. This suggests less intense mixing with oxygenated water. However, alongside sequences related to strictly anaerobic organisms were those also associated with aerobic and microaerophilic bacteria (Fig. 1a–c). Therefore, oxygen must be available in some areas. Nevertheless, merely one phylotype of group F Epsilonproteobacteria was encountered at Irina I (Fig. 1a). Judging from the group-specific characteristics of these bacteria, they are not only associated with lower growth temperatures but also with tolerance towards oxygen (Campbell et al., 2006). Members of this group were, however, detected in great diversity at Irina II and Site B. Their occurrence in the fluids next to anaerobic Desulfobulbaceae implicates mixing processes which have caused multiple biotopes to arise along the fluid pathways. The absence of Deltaproteobacteria at Irina I might indicate a limitation of sulfate or other oxidized sulfur species, or the influence of oxygen on the selection of bacteria.
The presence of thioautotrophic and methylotrophic symbionts of the vent mussel Bathymodiolus spp. in outflows at Irina II is not surprising, as Bathymodiolus assemblages colonize the entire surroundings (Kuhn et al., 2004; Lackschewitz et al., 2005). Predation or natural death of Bathymodiolus spp. could explain the occurrence of symbionts among free-living prokaryotes of the area.
Because thermophilic Methanococcales have been detected in low-temperature emissions, it has been argued that they might originate from subsurface environments (Huber et al., 2002; Takai et al., 2004a; Nakagawa et al., 2005a). They are independent of seawater-derived oxidants. The uniformity of the archaeal community at the LHF could suggest that parts of the Methanococcales originate from the subsurface.
Other environmental parameters
A single sequence at Irina I OTU IB488 and 10% of bacterial sequences from Irina II fluids were affiliated with the new group (RE1) (Fig. 1b), of which no cultured representatives exist. As all sequences of this group are derived from reduced environments, the name of RE1 for ‘reduced environment’ is proposed. It is conspicuous that, with the exception of two sequences retrieved from termites, all others originate from hydrothermal vent environments (Fig. 1b). The chemical conditions, i.e. low sulfide concentrations and high hydrogen concentrations (Table 1), could be favorable for the occurrence of RE1 members. However, several sequences of this group are derived from Snake Pit (Corre et al., 2001). Significantly higher sulfide concentrations (6 mM) have been determined at Snake Pit (Douville et al., 2002) than at the LHF (Table 1). The role these uncultured affiliates play in the ecosystem remains to be investigated.
For the first time, we report a sequence affiliated with the ANME-2 lineage of the Methanosarcinales from hot hydrothermal emissions. Interestingly, it was detected at Site B, where the lowest methane concentrations were measured (0.6 mM) (Table 1, Fig. 1d). Affiliates of ANME-2 mediate the anaerobic oxidation of methane and have been found in anoxic sediments, seep environments and also hydrothermally active sediment (e.g. Boetius et al., 2000; Orphan et al., 2001). The question of whether the sequence affiliated with the ANME-2 group is associated with methane oxidation remains open, as no significant methane oxidation rates were measured at diffusive and hot emission sites at the LHF (J. Felden, pers. commun.).
We would like to thank the captain and the crews of the RV Meteor and ROV QUEST (MARUM, Bremen) for helping us to obtain deep-sea vent samples. Further, we thank Dr Jörg Süling and Andrea Gärtner for assisting with the collection and handling of the samples, and Dr Siegi Ertl and Gunnar Schroll for measurements of methane concentrations. The authors wish to thank Dr Sven Petersen for his constructive comments on this manuscript. The work was supported by grants from the priority program 1144 of the German Science Foundation. This is publication no. 9 of the priority program 1144 “From Mantle to Ocean: Energy-, Material- and Life-cycles at Spreading Axes” of the DFG.
- 1999) Diversity of free-living and attached bacteria in offshore western mediterranean waters as depicted by analysis of genes encoding 16S rRNA. Appl Environ Microbiol 65: 514–522. , & (
- 2004) Early steps in microbial colonization processes at deep-sea hydrothermal vents. Environ Microbiol 6: 227–241. , , , , , & (
- 1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25: 3389–3402. , , , , , & (
- 2002) Phylogenetic composition of bacterioplankton assemblages from the Arctic Ocean. Appl Environ Microbiol 68: 505–518. & (
- 2000) A marine microbial consortium apparently mediating anaerobic oxidation of methane. Nature 407: 623–626. , , , , , , , , & (
- 1997) A new type of modern mineral-forming systems: black smokers of the hydrothermal field at 14°45′N latitude, Mid-Atlantic Ridge. Geol Ore Dep 39: 68–90. , , , & (
- 2006) Methane- and sulfur-metabolizing microbial communities dominate the Lost City hydrothermal field ecosystem. Appl Environ Microbiol 72: 6257–6270. , , & (
- 2006) The versatile ɛ-proteobacteria: key players in sulphidic habitats. Nature Rev Microbiol 4: 458–468. , , & (
- 1969) Spectrophotometric determination of hydrogen sulfide in natural waters. Limnol Oceanogr 14: 454–458. (
- 2003) The Ribosomal Database Project (RDP-II): previewing a new autoaligner that allows regular updates and the new prokaryotic taxonomy. Nucleic Acids Res 31: 442–443. , , et al. (
- 2001) Epsilonproteobacterial diversity from a deep-sea hydrothermal vent on the Mid-Atlantic Ridge. FEMS Microbiol Lett 205: 329–335. , & (
- 1992) Archaea in coastal marine environments. Proc Natl Acad Sci USA 89: 5685–5689. (
- 2003) Molecular characterization of sulfate-reducing bacteria in the Guaymas Basin. Appl Environ Microbiol 69: 2765–2772. , , , & (
- 2000) Genetic variation among endosymbionts of widely distributed vestimentiferan tubeworms. Appl Environ Microbiol 66: 651–658. , , , , & (
- 1997) High H2 and CH4 content in hydrothermal fluids from Rainbow site newly sampled at 36°14′N on the AMAR segment, Mid-Atlantic Ridge (diving FLORES cruise, July 1997). Comparison with other MAR sites. EOS 78: 832. , , , , , , & (
- 2002) The Rainbow vent fluids (36 degrees 14′N, MAR); the influence of ultramafic rocks and phase separation on trace metal content in Mid-Atlantic Ridge hydrothermal fluids. Chem Geol 184: 37–48. , , , , , , , & (
- 2006) KIPS – A new multiport valve-based all – teflon fluid sampling system for ROVs. EGU Meeting Vienna, Austria. Geophys Res Abstr 8: 07032. , , , & (
- 2002) Persephonella marina gen. nov., sp. nov. and Persephonella guaymasensis sp. nov., two novel, thermophilic, hydrogen-oxidizing microaerophiles from deep-sea hydrothermal vents. Int J Syst Evol Microbiol 52: 1349–1359. , , , , & (
- 1996) Environmental transmission of a sulfur-oxidizing bacterial gill endosymbiont in the tropical lucinid bivalve Codakia orbicularis. Appl Environ Microbiol 62: 2324–2330. , , , & (
- 2003) A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 52: 696–704. & (
- 2003) Microbial diversity of a sulphide spire located in the Edmond deep-sea hydrothermal vent field on the Central Indian Ridge. Geobiol 1: 119–127. , & (
- 2001) Initial indications of abiotic formation of hydrocarbons in the Rainbow ultramafic hydrothermal system, Mid-Atlantic Ridge. Earth Plan Sci Lett 191: 1–8. & (
- 2002) Temporal changes in archaeal diversity and chemistry in a mid-ocean ridge subseafloor habitat. Appl Environ Microbiol 68: 1585–1594. , & (
- 2003) Bacterial diversity in a subseafloor habitat following a deep-sea volcanic eruption. FEMS Microbiol Ecol 43: 393–409. , & (
- 1985) Thiomicrospira crunogena sp. nov., a colorless, sulfur-oxidizing bacterium from a deep-sea hydrothermal vent. Int J Syst Bacteriol 35: 422–424. , , & (
- 2002) Use of Fe(III) as an electron acceptor to recover previously uncultured hyperthermophiles: isolation and characterization of Geothermobacterium ferrireducens gen. nov., sp. nov. Appl Environ Microbiol 68: 1735–1742. , , & (
- 2001) An off-axis hydrothermal vent field near the Mid-Atlantic Ridge at 30°N. Nature 412: 145–149. , , et al. (
- 2002) Volcanoes, fluids, and life at mid-ocean ridge spreading centers. Ann Rev Earth Plan Sci 30: 385–490. , & (
- 2006) Bacterial and archaeal phylotypes associated with distinct mineralogical layers of a white smoker spire from a deep-sea hydrothermal vent site (9°N, East Pacific Rise). Environ Microbiol 8: 909–920. , , & (
- 2004) Mineralogical, geochemical, and biological investigations of hydrothermal systems on the Mid-Atlantic Ridge between 14°45′N and 15°05′N (HYDROMAR I). Cruise Report. [online] http://www.ifm-geomar.de/index.php?id=sppnews&L=1 , , et al. (
- 2005) Longterm study of hydrothermalism and biology at the Logatchev field, Mid-Atlantic Ridge at 14°45′N (revisit 2005; HYDROMAR II). Cruise Report. [online] http://www.ifm-geomar.de/index.php?id=sppnews&L=1 , , et al. (
- 1991) 16S/23S rRNA sequencing. Nucleic acid techniques in bacterial systematics (StackebrandtE & GoodfellowM, eds), pp 115–175. John Wiley & Sons, New York. (
- 1998) Desulfurobacterium thermolithotrophum gen. nov., sp. nov., a novel autotrophic, sulphur-reducing bacterium isolated from a deep-sea hydrothermal vent. Int J Syst Bacteriol 48: 701–711. , , , , , , & (
- 2001) Antagonistic interactions among marine pelagic bacteria. Appl Environ Microbiol 67: 4975–4983. & (
- 2003) Bacterial diversity in hydrothermal sediment and epsilonproteobacterial dominance in experimental microcolonizers at the Mid-Atlantic Ridge. Environ Microbiol 5: 961–976. , , , , & (
- 2004) ARB: a software environment for sequence data. Nucleic Acids Res 32: 1363–1371. , , et al. (
- 1978) Chemical exchange during hydrothermal alteration of basalt by seawater-I. Experimental results for major and minor components of seawater. Geochim Cosmochim Acta 42: 1103–1115. & (
- 1991) Evidence for the establishment of aphid-eubacterium endosymbiosis in an ancestor of four aphid families. J Bacteriol 173: 6321–6324. , , , , , & (
- 1993) Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA. Appl Environ Microbiol 59: 695–700. , & (
- 2005a) Variability in microbial community and venting chemistry in a sediment-hosted backarc hydrothermal system: impacts of subseafloor phase-separation. FEMS Microbiol Ecol 54: 141–155. , , , , , , , , & (
- 2005b) Nitratiruptor tergarcus gen. nov., sp. nov. and Nitratifractor salsuginis gen. nov., sp. nov., nitrate-reducing chemolithoautotrophs of the ɛ-Proteobacteria isolated from a deep-sea hydrothermal system in the Mid-Okinawa Trough. Int J Syst Evol Microbiol 55: 925–933. , , , & (
- 2005) Diversity of functional genes of methanogens, methanotrophs and sulfate reducers in deep-sea hydrothermal environments. Environ Microbiol 7: 118–132. , , , & (
- 2001) Comparative analysis of methane-oxidizing archaea and sulfate-reducing bacteria in anoxic marine sediments. Appl Environ Microbiol 67: 1922–1934. , , , , , , & (
- 2001) Evaluation of PCR-generated chimeras, mutations, and heteroduplexes with 16S rRNA gene-based cloning. Appl Environ Microbiol 67: 880–887. , , , , , & (
- 2007) Geochemistry of hydrothermal fluids from the ultramafic-hosted Logatchev field, 15°N MAR: temporal and spatial investigation. Chem Geol, in press. , , , & (
- 2004) Low archaeal diversity linked to subseafloor geochemical processes at the Lost City hydrothermal field, Mid-Atlantic Ridge. Environ Microbiol 6: 1086–1095. , , & (
- 1999) Ethylene and methane in the upper water column of the subtropical Atlantic. Biogeochemistry 44: 73–91. , , , , & (
- 2006) Methane dynamics in a microbial community of the Black Sea traced by stable carbon isotopes in vitro. Org Geochem 37: 1411–1419. , , , & (
- 1998) Organic synthesis during fluid mixing in hydrothermal systems. J Geophys Res 103: 513–528. & (
- 2003) Isolation and phylogenetic diversity of members of previously uncultivated Epsilonproteobacteria in deep-sea hydrothermal fields. FEMS Microbiol Lett 218: 167–174. , , , , , , & (
- 2004a) Geochemical and microbiological evidence for a hydrogen-based, hyperthermophilic subsurface lithoautotrophic microbial ecosystem (HyperSLiME) beneath an active deep-sea hydrothermal field. Extremophiles 8: 269–282. , , , , , & (
- 2004b) Thiomicrospira thermophila sp. nov., a novel microaerobic, thermotolerant, sulfur-oxidizing chemolithomixotroph isolated from a deep-sea hydrothermal fumarole in the TOTO caldera, Mariana Arc, Western Pacific. Int J Syst Evol Microbiol 54: 2325–2333. , , , , & (
- 2001) Biogeography and ecological setting of Indian Ocean hydrothermal vents. Science 294: 818–823. , , et al. (
- 2004) Diffuse flow hydrothermal fluids from 9° 50′N East Pacific Rise: origin, evolution and biogeochemical controls. The Subseafloor Biosphere at Mid-Ocean Ridges, Vol. 144 (WilcockWSD, DeLongEF, KelleyDS, BarossJA & CarySC, eds), pp. 245–268. Geophys Union Monogr Ser, Washington, DC. & (
- 2000) Distinguishing ultra-mafic from basalt-hosted submarine hydrothermal systems by comparing calculated vent fluid compositions. J Geophys Res 105: 8319–8340. & (
- 1992) The prokaryotes. The Methanogenic Bacteria (BalowsA, TrüperHG, DworkinM, HarderW & SchleiferK-H, eds), pp. 719–767. Springer-Verlag, New York. , & (