
of greenhouse gases (Sagan and Chyba, 1997), or that oceans
may have been partially covered by ice and warmed by sub-
marine volcanism and periodic impacts (Bada et al., 1994).
Evidence and controversy for early life
The need to understand the timing of and conditions for the origin
of life is one of the principle motivations for assessing the early
Archean environment. The primary requirements for evolution
of life are organic molecules, a source of energy, and liquid water.
Organic molecules could have been delivered to Earth by carbo-
naceous meteorites and comets, and energy was available from
the Sun and terrestrial volcanism. The precipitation of liquid
water from an early steam-rich atmosphere was thus the final
ingredient for an environment where life could have evolved dur-
ing the period 4.4–4.0 Ga, perhaps to be extinguished by large
bolide impacts or during the late heavy bombardment at 3.9
Ga. Theoretical limits of the habitability of the early Earth are
thoroughly discussed elsewhere (see Nisbet and Sleep, 2001),
but here we focus on evidence for early life from the rock record.
The earliest evidence for life is a distinctive carbon isotope
signature from metamorphosed sedimentary rocks of southwes-
tern Greenland. Low carbon isotope ratios (
13
C/
12
C) in reduced
sedimentary carbon are commonly the result of isotope fractiona-
tion by biological pathways, and thus are taken as a “fingerprint”
of ancient life even in the absence of preserved fossils (Schi-
dlowski, 2001). While some studies have been controversial,
the best evidence for early life comes from southwest Greenland:
low carbon isotope ratios of graphite particles in clastic sedimen-
tary rocks from 3.8 to 3.7 Ga rocks at Isua (Rosing, 1999). These
rocks are preserved in low-strain zones, were clearly waterlain,
and the graphite may represent original organic detritus.
The earliest fossil evidence for life are 3.5 Ga microscopic
structures in the Apex chert of Australia as well as numerous
occurrences of stromatolites (mounds produced by photosyn-
thetic microbes). These microstructures are interpreted as being
the remains of various Archean microbes (Schopf, 1993).
This claim of diversity of life has been challenged by Brasier
et al. (2002), based on morphology of the features as well as
a hydrothermal origin of the host-rock. However, the kero-
gen-like Raman spectra and low carbon isotope ratios are
strong evidence of biologic activity (Schopf et al., 2002).
Furthermore, abundant stromatolites are found in associated
rocks. The association of microfossils with seafloor hydrother-
mal systems has been recognized in rocks as old as 3.5 Ga
(Van Kranendonk, 2001), supporting the hypothesis that life
originally evolved near submarine vents or springs in early
Archean oceans (e.g., Nisbet and Sleep, 2001).
William H. Peck and John W. Valley
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ARCHEAN ENVIRONMENTS 37