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Table T16. Culturing efforts, Hole U1372A.

Core, section,
interval (cm)
Media Vials
inoculated
(N)
Growth
330-U1372A-
4R-3, 71–82                   Autotrophic S oxidizers 2 ND*
Heterotrophic S oxidizers 2 ND*
Autotrophic SO42– reducers 2 ND*
Heterotrophic SO42– reducers 2 ND*
Autotrophic methanogens 2 ND*
Heterotrophic methanogens 2 ND*
Autotrophic Fe reducers 2 ND*
Heterotrophic Fe reducers 2 ND*
Autotrophic Fe oxidizers 2 ND*
Aerobic heterotrophs 3 ND*
8R-5, 27–35         Autotrophic Fe reducers 2 ND
Heterotrophic Fe reducers 2 ND
Autotrophic Fe oxidizers 2 ND
Aerobic heterotrophs 2 +
Heterotrophic SO42– reducers 1 Not sure
18R-2, 44–51           Autotrophic S oxidizers 2 +
Heterotrophic S oxidizers 2 +
Autotrophic Fe reducers 2 ND
Heterotrophic Fe reducers 2 ND
Autotrophic Fe oxidizers 2 ND
Aerobic heterotrophs 2 +
29R-1, 21–31           Autotrophic S oxidizers 2 +
Autotrophic SO42– reducers 2
Autotrophic Fe reducers 2 ND
Heterotrophic Fe reducers 2 ND
Autotrophic Fe oxidizers 2 ND
Aerobic heterotrophs 2 +

* = growth could not be determined via turbidity because inoculum itself was turbid. † = growth could not be determined because Fe oxides that are part of media are very turbid, and changes in turbidity due to cell growth were impossible to detect by eye. ‡ = turbidity was apparent but may have been due to inoculum (this was only culture experiment inoculated with a rock chip, which likely had particles on it to begin with). + = only one vial was positive, – = no growth.

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