Quartz |
Adenine |
200–300 nm |
Under N2
|
Under O2
|
Photo-oxidation by O2 (Oro & Holzer 1979). |
Quartz |
Glycine |
200–300 nm |
Under N2
|
Under O2
|
Photo-oxidation by O2 (Oro & Holzer 1979). |
Quartz |
Naphthalene |
200–300 nm |
x |
Under O2/N2
|
Photo-oxidation by O2 (Oro & Holzer 1979). |
Murchison meteorite |
Indigenous organics |
200–300 nm |
x |
Under O2/N2
|
Photo-oxidation by O2 (Oro & Holzer 1979). |
Palagonite |
Glycine |
210–710 nm |
x |
Under Martian-like atmosphere |
Photolysis into CH4, C2H6, C2H4 (Stoker & Bullock 1997). |
JSC Mars-1 and Salten Skov Martian soil analogs |
Indigenous amino acids |
190–325 nm |
x |
Under Martian-like atmosphere |
Decomposition induced by radicals produced by photolysis of water condensed onto minerals (Garry et al. 2006). |
JSC Mars-1 Martian soil analog |
Carboxylic acids α-aminoisobutyric acid (AIB), mellitic acid, phthalic acid, and trimesic acid |
Solar radiation > 200 nm |
x |
Under low Earth orbit conditions |
Decomposition induced by radicals/oxidants produced by TiO2–photocatalysis (Stalport et al. 2010). |
I-MAR Martian regolith simulant |
Amino acids L-Alanine, L-valine, L-aspartic acid, L-glutamic acid, and glycine |
210–900 nm |
x |
Under Martian-like atmosphere |
Photolytic oxidation up to UV penetration depth, then decomposition induced by radicals formed from condensed atmospheric water vapor diffused into the regolith (Johnson & Pratt 2011). |
Aqueous suspensions of anatase, goethite, and hematite |
Carboxylic, hydroxycarboxylic, and aminocarboxylic acids, carboxylated aromatics, amino acids and peptides |
355 nm |
x |
Under N2
|
Decarboxylation initiated by charge transfer from the metal oxide to the adsorbate. Specifically, anatase, goethite, and hematite feature a similar photocatalytic activity for aromatic, carboxylic, and hydroxycarboxylic acids, while for α-amino acids and peptides hematite has reduced activity (Shkrob et al. 2010). |
Aqueous suspensions of anatase, goethite, and hematite |
Nucleic acid components |
355 nm |
Only for double-stranded oligoribonucleotides and DNA |
Under N2
|
Oxidation of purine nucleotides leads to formation of purine radical cations and sugar-phosphate radicals. In the case of pyrimidine nucleotides other than thymine only the sugar-phosphate moiety undergoes oxidation, while deprotonation from the methyl group of the base occurs for thymine derivatives. Single-stranded (ss) oligoribonucleotides and wild-type ss RNA are oxidized at purine sites, while double-stranded (ds) oligoribonucleotides and DNA show high stability against oxidation (Shkrob et al. 2011). |
Aqueous suspensions of montmorillonite and kaolinite |
DNA |
266 nm |
Under terrestrial ambient conditions |
x |
Photoprotection due to specific molecule-mineral interactions; specifically, a change in DNA configuration from B to A when adsorbed on the mineral surface, which is more compact and its binding to the surface sites may take place through electrostatic and/or hydrogen bonds likely stabilizing the molecule (Scappini et al. 2004). |
Aqueous suspensions of montmorillonite |
RNA molecule ADHR1 |
254 nm |
Under terrestrial ambient conditions |
x |
Photoprotection due to specific molecule-mineral interactions (Biondi et al. 2007). |
Nontronite |
Glycine and adenine |
190–400 nm |
Under N2
|
x |
Photoprotection is not only due to mechanical shielding, but also stabilizing molecule-mineral interactions, such as electrostatic interactions of the molecules in the interlayers and/ or on the edges of nontronite allowing a more efficient energy dissipation and/or easier recombination for the fragments of the photo-dissociated molecules (Poch et al. 2015). |
Nontronite |
Urea |
190–400 nm |
x |
Under N2
|
Catalysis in urea photo-oxidation and decomposition, maybe due to chelation with Fe3+ ions (Poch et al. 2015). |
Smectites montmorillonite, nontronite and saponite |
25 Amino acids |
200–400 nm |
Under Martian-like conditions |
x |
Photoprotection by mechanical shielding effect (dos Santos et al. 2016). |
Sulfates gypsum and jarosite |
25 Amino acids |
200–400 nm |
Under Martian-like conditions |
x |
Photoprotection due to low UV absorbance of sulfates or entrapment of amino acids upon recrystallization of partially dissolved sulfate (dos Santos et al. 2016). |
Augite, enstatite, hematite and basaltic lava |
25 Amino acids |
200–400 nm |
x |
Under Martian-like conditions |
Photocatalytic activity due to iron(II) reactions (dos Santos et al. 2016). |
Calcite, calcium sulphate, kaolinite, clay-bearing Atacama desert soil + 0.6% NaClO4
|
Purine, pyrimidine and uracil |
200–400 nm |
Under Martian-like conditions |
x |
Photoprotection mechanism not specified (Ertem et al. 2017). |
Ferric oxide + 0.6% NaClO4
|
Purine, pyrimidine and uracil |
200–400 nm |
x |
Under Martian-like conditions |
Complete decomposition before UV irradiation (Ertem et al. 2017). |
Magnesium oxide and forsterite |
Adenine, uracil, cytosine, and hypoxanthine |
185–2000 nm |
x |
Under vacuum |
Catalysis likely due to a proximity effect (Fornaro et al. 2013). |
Lizardite, antigorite and apatite |
AMP and UMP |
200–930 nm |
Under Martian-like conditions |
x |
Various photoprotection mechanisms: mechanical shielding/stabilizing molecule-mineral interactions for lizardite and antigorite, photo-luminescence for apatite (Fornaro et al. 2018). |
Labradorite, natrolite, hematite, forsterite |
AMP and UMP |
200–930 nm |
x |
Under Martian-like conditions |
Remarkable catalytic activity of labradorite and natrolite, likely due to photo-ionization phenomena that may occur inside the mineral matrix promoting redox processes. For hematite and forsterite the catalytic activity is not so high, maybe due to the opacity of iron to UV radiation (Fornaro et al. 2018). |