SP-1231 Fig. II.6.2.2/2. Fossil rod-shaped bacteria (sausage-shaped structures) embedded <str<strong>on</strong>g>in</str<strong>on</strong>g> gra<str<strong>on</strong>g>in</str<strong>on</strong>g>y biofilm. From <str<strong>on</strong>g>the</str<strong>on</strong>g> Hooggenoeg Formati<strong>on</strong>, Onverwacht Group, South Africa (age 3445-3472 Myr). 160 II.6.2.2 Microscopic Scale On a microscopic scale, biogenic structures that can be seen <str<strong>on</strong>g>in</str<strong>on</strong>g>clude: • undulat<str<strong>on</strong>g>in</str<strong>on</strong>g>g biofilm lam<str<strong>on</strong>g>in</str<strong>on</strong>g>ae of <str<strong>on</strong>g>the</str<strong>on</strong>g> order of 100 µm; • microfossils with a maximum dimensi<strong>on</strong>
<str<strong>on</strong>g>Search</str<strong>on</strong>g><str<strong>on</strong>g>in</str<strong>on</strong>g>g <str<strong>on</strong>g>for</str<strong>on</strong>g> signs of extant or ext<str<strong>on</strong>g>in</str<strong>on</strong>g>ct life <str<strong>on</strong>g>in</str<strong>on</strong>g>cludes <str<strong>on</strong>g>the</str<strong>on</strong>g> evaluati<strong>on</strong> of direct evidence <str<strong>on</strong>g>in</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> <str<strong>on</strong>g>for</str<strong>on</strong>g>m of preserved fossils, ei<str<strong>on</strong>g>the</str<strong>on</strong>g>r m<str<strong>on</strong>g>in</str<strong>on</strong>g>eralised or as organic rema<str<strong>on</strong>g>in</str<strong>on</strong>g>s, as well as a more <str<strong>on</strong>g>in</str<strong>on</strong>g>direct approach utilis<str<strong>on</strong>g>in</str<strong>on</strong>g>g geochemical and/or isotopic proxies <str<strong>on</strong>g>for</str<strong>on</strong>g> past biologically-driven processes and <str<strong>on</strong>g>the</str<strong>on</strong>g>ir metabolic products, as discussed <str<strong>on</strong>g>in</str<strong>on</strong>g> Secti<strong>on</strong> II.5. As such, <str<strong>on</strong>g>the</str<strong>on</strong>g> presence of organic compounds and/or certa<str<strong>on</strong>g>in</str<strong>on</strong>g> chemical elements that represent important build<str<strong>on</strong>g>in</str<strong>on</strong>g>g blocks of life (i.e. C, H, N, S, P), <str<strong>on</strong>g>the</str<strong>on</strong>g>ir specific isotopic compositi<strong>on</strong>s and <str<strong>on</strong>g>the</str<strong>on</strong>g>ir presence as m<str<strong>on</strong>g>in</str<strong>on</strong>g>eral matter of presumed biological orig<str<strong>on</strong>g>in</str<strong>on</strong>g> might provide evidence <str<strong>on</strong>g>for</str<strong>on</strong>g> (or aga<str<strong>on</strong>g>in</str<strong>on</strong>g>st) <str<strong>on</strong>g>the</str<strong>on</strong>g> presence or past presence of life. In additi<strong>on</strong> to <str<strong>on</strong>g>the</str<strong>on</strong>g> exclusive search <str<strong>on</strong>g>for</str<strong>on</strong>g> evidence of life, a thorough characterisati<strong>on</strong> of <str<strong>on</strong>g>the</str<strong>on</strong>g> present and past envir<strong>on</strong>mental c<strong>on</strong>diti<strong>on</strong>s should be a prerequisite. In comparis<strong>on</strong> to terrestrial sett<str<strong>on</strong>g>in</str<strong>on</strong>g>gs, a wide variability <str<strong>on</strong>g>in</str<strong>on</strong>g> habitats do show flourish<str<strong>on</strong>g>in</str<strong>on</strong>g>g life. However, certa<str<strong>on</strong>g>in</str<strong>on</strong>g> physical and chemical parameters provide boundary c<strong>on</strong>diti<strong>on</strong>s that limit its survival. Of particular <str<strong>on</strong>g>in</str<strong>on</strong>g>terest are m<str<strong>on</strong>g>in</str<strong>on</strong>g>erals that presumably <str<strong>on</strong>g>for</str<strong>on</strong>g>med through biological processes, i.e. biom<str<strong>on</strong>g>in</str<strong>on</strong>g>erals. Pyrite (FeS 2) is a ubiquitous m<str<strong>on</strong>g>in</str<strong>on</strong>g>eral <str<strong>on</strong>g>in</str<strong>on</strong>g> terrestrial sediments and frequently of biogenic orig<str<strong>on</strong>g>in</str<strong>on</strong>g>. A key process <str<strong>on</strong>g>in</str<strong>on</strong>g> its <str<strong>on</strong>g>for</str<strong>on</strong>g>mati<strong>on</strong> is <str<strong>on</strong>g>the</str<strong>on</strong>g> bacterial reducti<strong>on</strong> of sulphate to H 2S and subsequent reacti<strong>on</strong> with ir<strong>on</strong> m<str<strong>on</strong>g>in</str<strong>on</strong>g>erals, to <str<strong>on</strong>g>for</str<strong>on</strong>g>m ir<strong>on</strong> sulphide. <str<strong>on</strong>g>The</str<strong>on</strong>g> <str<strong>on</strong>g>for</str<strong>on</strong>g>mati<strong>on</strong> of sedimentary pyrite, specifically of biological orig<str<strong>on</strong>g>in</str<strong>on</strong>g>, and <str<strong>on</strong>g>the</str<strong>on</strong>g> relati<strong>on</strong>ship between pyrite morphology, orig<str<strong>on</strong>g>in</str<strong>on</strong>g> and depositi<strong>on</strong>al envir<strong>on</strong>ment, has been studied <str<strong>on</strong>g>for</str<strong>on</strong>g> many decades (e.g. Berner, 1970; Goldhaber & Kaplan, 1974; Berner, 1984; Morse et al., 1987; Scho<strong>on</strong>en & Barnes, 1991; Sawlowicz, 1993; Wilk<str<strong>on</strong>g>in</str<strong>on</strong>g> et al., 1996, Wilk<str<strong>on</strong>g>in</str<strong>on</strong>g> & Barnes, 1997). Fur<str<strong>on</strong>g>the</str<strong>on</strong>g>rmore, pyrite has been c<strong>on</strong>sidered as a potential orig<str<strong>on</strong>g>in</str<strong>on</strong>g> of life (e.g. Wächtershäuser, 1988; Russel et al., 1989; 1990). Of all <str<strong>on</strong>g>the</str<strong>on</strong>g> possible biogenic morphologies, framboidal pyrite c<strong>on</strong>sist<str<strong>on</strong>g>in</str<strong>on</strong>g>g of m<str<strong>on</strong>g>in</str<strong>on</strong>g>ute pyritic gra<str<strong>on</strong>g>in</str<strong>on</strong>g>s resembl<str<strong>on</strong>g>in</str<strong>on</strong>g>g raspberries (Rust, 1935) has received most attenti<strong>on</strong>. Generally, <str<strong>on</strong>g>the</str<strong>on</strong>g> sizes of <str<strong>on</strong>g>the</str<strong>on</strong>g>se framboids range from 5 mm to 20 mm, but framboids as large as 250 mm have occasi<strong>on</strong>ally been observed. Alternatively, framboids as small as 1 mm were also seen. Agglomerati<strong>on</strong> of <str<strong>on</strong>g>in</str<strong>on</strong>g>dividual framboids might result <str<strong>on</strong>g>in</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> so called polyframboids with sizes rang<str<strong>on</strong>g>in</str<strong>on</strong>g>g from 35 mm to 900 mm (average 50- 200 mm). Thus, a c<strong>on</strong>t<str<strong>on</strong>g>in</str<strong>on</strong>g>uous spectrum of sizes, microframboids–framboids– polyframboids, exists (e.g. Sawlowicz, 1993). In terrestrial sett<str<strong>on</strong>g>in</str<strong>on</strong>g>gs, framboidal pyrite is most comm<strong>on</strong> <str<strong>on</strong>g>in</str<strong>on</strong>g> recent and ancient sedimentary envir<strong>on</strong>ments, but has also been reported from magmatic rocks or hydro<str<strong>on</strong>g>the</str<strong>on</strong>g>rmal occurrences (e.g. Sassano & Schrijver, 1989). <str<strong>on</strong>g>The</str<strong>on</strong>g> framboidal texture is usually associated with pyrite, but has also team III: <str<strong>on</strong>g>the</str<strong>on</strong>g> <str<strong>on</strong>g>in</str<strong>on</strong>g>specti<strong>on</strong> of subsurface aliquots and surface rocks/II.6 Fig. II.6.2.2/3. Fossil coccoid bacteria 1 µm <str<strong>on</strong>g>in</str<strong>on</strong>g> diameter show<str<strong>on</strong>g>in</str<strong>on</strong>g>g cellular divisi<strong>on</strong>. <str<strong>on</strong>g>The</str<strong>on</strong>g>se structures have a size typical <str<strong>on</strong>g>for</str<strong>on</strong>g> terrestrial bacteria. High magnificati<strong>on</strong>s are needed to image <str<strong>on</strong>g>the</str<strong>on</strong>g>m (>100 times with resoluti<strong>on</strong>s of at least 0.25 µm per pixel). II.6.3 Investigati<strong>on</strong> of Biom<str<strong>on</strong>g>in</str<strong>on</strong>g>erals 161
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SP-1231 Exobiology
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Cover Fossil coccoid bacteria, 1 µ
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4 I.5 Potential Non-Martian Sites <
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6 6.2 Imaging of F
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The Exobio
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pyrolysis, or similar techniques, f
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Ignasi Casanova, Institute
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I AN EXOBIOLOGICAL VIEW OF THE SOLA
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SP-1231 18 surface pressure of CO 2
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SP-1231 20 10 bar befor</st
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SP-1231 22 kilometres in</s
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SP-1231 24 Laboratory Investigation
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I.3 Limits of Life
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temperatures of 95-106ºC. This sug
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(mainly found <str
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cannot exclude fin
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Responses to Cosmic Radiation <stro
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acid to identify the</stron
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Horneck, G. (1993). Responses of Ba
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SP-1231 Fig. I.4.2.2/1. Size distri
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SP-1231 Fig. I.4.2.2/4. Evaporite w
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SP-1231 Fig. I.4.2.3/1A (left). Net
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SP-1231 48 A detailed chemical anal
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SP-1231 Fig. I.4.3.1.1/1. Scheme of
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SP-1231 Fig. I.4.3.1.2/1. A: Compar
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SP-1231 54 I.4.3.2.1 Sedimentary Or
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SP-1231 56 The iso
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SP-1231 Fig. I.4.3.2.3/1. Cholester
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SP-1231 60 References regard to non
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SP-1231 62 Klein,
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SP-1231 64 ities in</strong
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SP-1231 Fig. I.5.1.1/1. A 34×42 km
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SP-1231 Fig. I.5.2.1/1. Titan’s a
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SP-1231 Fig. I.5.2.2/2. Modelled Ti
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SP-1231 72 Galileo: images availabl
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SP-1231 74 TABLE I.6.2/1 EVIDENCE O
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SP-1231 I.6.3 What to Searc
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SP-1231 78 I.7.3 Organic Chemistry
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II.1 Introduction The</stro
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II.2 The Planet Ma
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cover the range 4.
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The depletion of c
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valley networks (Fig. II.2.5/2) are
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plate tectonic evidence has been ob
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Table II.2.7.4/1. Potential Mars <s
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II.3 The Martian M
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principal atmosphe
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Lines of evidence
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indicated by carbo
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quest for
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Anders, E. (1989). Prebiotic organi
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