 
 
The oldest biofossils
  
  The geologic source of the 3.556 billion-year-old samples proved questionable, 
  but Schopf and others reexamined the 3.465 billion-year-old filaments for their 
  authenticity with Laser-Raman spectroscopy, focusing in particular on the compositional 
  aspects of the fossilized materials (Nature, v. 416, 2002, p. 73-76). 
  The new data reasserted the biogenicity, or biological origin, of the Apex chert 
  filaments. Other investigators, however, do not agree with these conclusions. 
  They contend that Schopf's fossils are likely artifacts, based on reinterpretations 
  of the Warrawoona structures  after new geologic mapping, more extensive 
  optical and electron microscopy, stable isotopic analyses, and Raman spectroscopy 
  of other carbonaceous materials.
  
  Martin Brasier at the University of Oxford and others suggest that the locality 
  of the Apex chert microfossils is not, as previously suggested, a bedded conglomerate, 
  but rather a metalliferous hydrothermal vein that formed at temperatures of 
  250 to 350 C  more than 100 C hotter than even the most optimistic view 
  of the upper limit for life (Nature, v. 416, 2002, p. 76-81). They further 
  argue that abiotic synthesis may be responsible for the reduced carbon compounds 
  analyzed in the chert and their light isotopic signatures. Jill Pasteris and 
  Brigitte Wopenka of Washington University take further issue with the Raman 
  analysis of the Apex fossils (Nature, v. 420, 2002, p. 476-477). They 
  note that this technique can in no way unambiguously identify biogenic carbon, 
  citing numerous examples of clearly non-biogenic carbon compounds that yield 
  spectra indistinguishable from Schopf's spectra. In their reply, Schopf and 
  colleagues state that Raman spectra can hint at biogenicity, but add that these 
  data should always be interpreted in connection with other lines of evidence 
   evidence, which, however, is also being reevaluated (Nature, v. 
  420, 2002, p. 477).
The oldest chemofossils
  
  In May of last year, Chris Fedo and Martin Whitehouse reported evidence that 
  directly contradicts the origin of the Greenland rocks that harbor the oldest 
  chemofossils (Science, v. 296, 2002, p. 1448-1452). What Mojzsis and 
  colleagues described as a metamorphosed sedimentary banded iron formation, Fedo 
  and Whitehouse interpreted as an ultramafic igneous rock. This reinterpretation 
  is largely based on trace element comparisons between this and various igneous 
  rocks and on a different reading of the regional geologic history. The new view, 
  if accurate, precludes that the isotopically light, graphitic carbon analyzed 
  by Mojzsis' group represents a biological signature. Whether or not the rocks 
  in question are sedimentary in origin remains unresolved, and, consequently, 
  so does the validity of the chemofossils at about 3.8 billion years (Palin, 
  Science, v. 298, 2002, p. 961).
Sunlight-independent microbial 
  metabolism
  
  Solar radiation provides energy to photosynthetic life, driving the progression 
  of otherwise thermodynamically unfavorable reactions. A few studies notwithstanding, 
  there is a consensus, however, that the earliest organisms on Earth were chemotrophs 
  and not phototrophs. In addition, approximately the first billion years of life 
  predated oxygenic photosynthesis. Hence, finding extant communities that live 
  completely independent from photosynthesis is of great interest. Such communities 
  and their environments would provide significant clues not only for understanding 
  life's origin on Earth, but also for elucidating extraterrestrial ecosystems 
  {emdash} most directly, subsurface abodes for microbes on Mars and Europa.
  
  In January 2002, Francis Chapelle and others described a hydrogen-based microbial 
  community 200 meters down in the subsurface hydrothermal groundwater of Lidy 
  Hot Springs in Idaho (Nature, v. 415, 2002, p. 312-315). Based on three 
  different culturing-independent molecular techniques, they determined that more 
  than 95 percent of the microbial population belonged to the domain Archaea (which 
  together with the domain Bacteria defines the prokaryotes); no eukaryotes and 
  only 1 to 5 percent Bacteria were present. Further, phylogenetic analyses revealed 
  that more than 90 percent of the archaeal sequences were most closely related 
  to methanogens  strict anaerobes that use carbon dioxide to oxidize hydrogen, 
  forming methane and water. Geochemical analyses showed that neither organic 
  carbon nor oxygen, which are common products of photosynthesis, figured in the 
  microbial metabolism at this site. Chapelle and colleagues argue that hot water-rock 
  interactions produced the hydrogen, which serves as the primary energy for these 
  subsurface communities.
  
  Hydrogen is also a critical source of energy and reducing power in other continental 
  and marine hydrothermal ecosystems. A recent review on this topic by Anna-Louise 
  Reysenbach and Everett Shock (Science, v. 296, 2002, p. 1077-1082) reminds 
  us that methanogenesis and sulfur-reduction  two hydrogen-consuming processes 
   are common metabolic strategies of primary producers deep in the global 
  phylogenetic tree of life. Many high temperature Archaea and Bacteria, most 
  of which thrive in the dark subsurface, are fueled by thermodynamically favorable, 
  but kinetically inhibited redox reactions. Reysenbach and Shock also note that 
  both genomes and rocks are "records of evolutionary changes;" once 
  encoded and annotated, they may reveal how Earth became habitable first to chemosynthetic, 
  most likely thermophilic, single-celled life  later to photosynthesizers, 
  eukaryotes, and ultimately the explosion of multicellular organisms.
  
  Expanding the field
  
  Although the timing and process of life's origin remain obscured and the extent 
  to which life inhabits Earth's subsurface and extraterrestrial planets remains 
  unbounded, the sandbox in which a geomicrobiologist plays is rapidly expanding. 
  Rovers will scour the martian surface next year looking for clues to life. Ocean 
  and continental drilling programs are aggressively incorporating  in fact 
  rallying around  geomicrobiology. This year, the National Science Foundation 
  will fund its first research proposals through the Biogeosciences Program. New 
  journals are targeting the biology-geology interface; Geobiology will 
  publish its inaugural volume later this year. In short, the field of geomicrobiology 
  is more dynamic than ever, and the questions being pursued hit at the core of 
  life on Earth 
 and elsewhere.
  
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