『Abstract
Carbonaceous matter (CM) from ca. 3.5 Ga hydrothermal black cherts
of the Pilbara Craton of Western Australia and the Barberton Greenstone
Belt of South Africa yielded transmission electron microscopy
(TEM) images that are suggestive of microbial remains and possible
remnants of microbial cell walls. These are compared to a potential
modern analogue, the hyperthermophilic Methanocaldococcus jannaschii,
derived from an active seafloor hydrothermal environment and cultured
under similar conditions. A striking resemblance to the early
Archaean forms was evident in wall structure and thermal degradation
mode. Cell disintegration of the cultures occurred at 100℃ marking
the limits f life. Complete disintegration, deformation and shrinkage
occurred at 132℃. A multidisciplinary approach to the characterisation
of the CM was undertaken using organic petrology, TEM coupled
with electron dispersive spectral analysis (EDS), high resolution
TEM (HRTEM) to determine molecular ordering, and elemental and
carbon isotope geochemistry. Reflectance measurements of the CM
to determine thermal stress yielded a range of values corresponding
to several populations, and pointing to different sources and
processes The δ13C values of Dresser Formation CM (-36.5
o -32.1‰) are negatively correlated with TOC (0.13-0.75%) and
positively correlated with C/N ratio (134-569), which is interpreted
to reflect the relative abundance of high Ro/oxidised/recycled
CM and preferential loss of 12C and N during thermal
maturation. TEM observations, inferred carbon isotopic heterogeneity
and isotope fractionations of -27 to -32‰ are consistent with
the activity of chemosynthetic microbes in a seafloor hydrothermal
system where rapid silicification at relatively low temperature
preserved the CM.
Keywords: Archaean; Pilbara Craton; Barberton Greenstone Belt;
Carbonaceous matter; Methanocaldococcus jannaschii; Transmission
electron microscopy; Carbon isotopes』
1. Introduction
2. General geology and methods of study
2.1. Geological setting
2.2. Sample processing
2.3. Microbiological procedures
2.4. Organic petrology
2.5. Scanning and transmission electron microscopy
2.6. Carbon isotope analysis
2.7. Total organic carbon (TOC) and elemental analysis
3. Results
3.1. Organic petrology
3.2. Scanning and transmission electron microscopy
3.3. Carbon isotopes and elemental composition
4. Discussion
4.1. Temperatures obtained from reflectance (Ro)
4.2. Comparison with an extant hyperthermophile
4.3. Origin of CM from carbon isotopes and elemental composition
5. Conclusion
Acknowledgments
References