2001
DOI: 10.1128/aem.67.2.827-833.2001
|View full text |Cite
|
Sign up to set email alerts
|

Discovery and Description of Giant Submarine Smectite Cones on the Seafloor in Eyjafjordur, Northern Iceland, and a Novel Thermal Microbial Habitat

Abstract: With the submersible JAGO and by scuba diving we discovered three remarkable geothermal cones, rising 33, 25, and 45 m from the seafloor at a depth of 65 m in Eyjafjordur, northern Iceland. The greatest geothermal activity was on the highest cone, which discharged up to 50 liters of freshwater per s at 72°C and pH 10.0. The cones were built up from precipitated smectite, formed by mixing of the hot SiO 2 -rich geothermal fluid with the cold Mg-rich seawater. By connecting a rubber hose to one outflow, about 24… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

5
78
0
1

Year Published

2003
2003
2024
2024

Publication Types

Select...
6
2
1

Relationship

0
9

Authors

Journals

citations
Cited by 91 publications
(84 citation statements)
references
References 22 publications
5
78
0
1
Order By: Relevance
“…We speculate that exchange occurs by movement of groundwater through the permeable tephra and basalt that underlies western Vatnajökull (Flowers et al, 2003). Unattached cells are readily transported through basalt (Entry and Farmer, 2001;Marteinsson et al, 2001). The high similarity of Sulfuricurvum sequences from all of our samples and enrichments suggests that it derives from a single population beneath Vatnajö kull.…”
Section: Discussionmentioning
confidence: 81%
See 1 more Smart Citation
“…We speculate that exchange occurs by movement of groundwater through the permeable tephra and basalt that underlies western Vatnajökull (Flowers et al, 2003). Unattached cells are readily transported through basalt (Entry and Farmer, 2001;Marteinsson et al, 2001). The high similarity of Sulfuricurvum sequences from all of our samples and enrichments suggests that it derives from a single population beneath Vatnajö kull.…”
Section: Discussionmentioning
confidence: 81%
“…C-J enrichments had addition of 50 ml of 100Â yeast-acetate medium and were incubated with 80%/20% H 2 /CO 2 and 0.025% final wt v À 1 Na 2 S 9H 2 O. A-J enrichments were the same as C-J, but incubated aerobically with ambient headspace. Additional enrichments used R 2 A medium and 162 Thermus medium (Degryse et al, 1978), both aerobically with ambient headspace, and Thermotoga ('Toga') medium (Marteinsson et al, 1997) and YPS medium (Marteinsson et al, 2001) under pure N 2 headspace. Growth in enrichments was confirmed with phase-contrast microscopy (Olympus BX51).…”
Section: Enrichment Culturesmentioning
confidence: 99%
“…The high temperature and the casing of the borehole down to 165 m isolates the bottom environment from the upper layers or surface microorganisms (Ólafsson and Jakobsson, 2009). The high sterilizing temperature atop the borehole suggest indigenous subterrestrial microbiota that have probably disseminated from the below faults and cracks of the seafloor in a similar manner as has been reported for other various subterrestrial environments, geothermal boreholes in Reykjavík (Marteinsson et al, 2001a), fresh water hydrothermal vent cones in Eyjafjörður (Marteinsson et al, 2001b) and in subglacial lakes on Vatnajökull (Marteinsson et al, 2013). Furthermore, our results on the microbial diversity support such deep indigenous subterrestrial microbiota speculations as our 16S rRNA gene sequence showed only similarity to uncultivated taxon originated from the deep biosphere.…”
Section: Subsurface Samplesmentioning
confidence: 85%
“…Filters were stored in DNA extraction buffer (0.1 M pH 8.0 Tris buffer, 0.1 M pH 8.0 Na-EDTA, 0.1 M phosphate buffer, 1.5 M NaCl and 0.5% cetyl trimethyl ammonium bromide) at À80 1C. DNA extraction from filters was performed as described by Marteinsson et al (2001b). DNA was also extracted from 1.5 ml of sample that was centrifuged, the pellet re-suspended in lysis buffer consisting of Tris buffer (50 mM, pH 7.6), EDTA (1 mM, pH 8.0), 0.5% Tween-20 (Sigma-Aldrich, St Louis, MO, USA) and 200 mg ml À1 proteinase K, the buffer incubated for 2 h at 55 1C and then heated to 95 1C for 5 min.…”
Section: Enrichment Culturesmentioning
confidence: 99%