Adam Johnson Department of Molecular and Cellular Biochemistry

Lisa M. Pratt Department of Geological Sciences

Indiana University Bloomington, Indiana Introduction

€ Recent activity on Mars has rekindled thoughts of life on the surface and subsurface € Thus far, the search for organic carbon and biomarkers on Mars yielded negative results y Active oxidation process y Hypothesized oxidants include: ○ Photochemical ○ Ionizing radiation ○ Peroxides and oxides/hydroxides ○ Chemical reactivity of the regolith (Fenton) € Work must be done to determine cumulative effects, primary mechanisms and kinetics of organic matter oxidation Experimental Goals

€ Perform long term simulation study with accurate mimicking of Mars surface conditions and regolith composition € Investigate the cumulative effects of photochemical and regolith reactivity on biomarker oxidation y Investigate the effects of depth below the profile surface y Correlate oxidation kinetics with various reaction pathways (UV, peroxide, Fenton oxidation) What Biomarker?

Dextrorotary Alanine Levorotary Alanine

€ 50% dry cell weight € Moderately good preservation potential € Optical activity differentiates from abiotic forms Indiana Mars Analog Regolith Simulant-2 (I-MARS-2) € Holocene andesitic basalt w/ olivine € Various iron oxides, phyllosilicates, iron sulfates and sulfate salts Mars Simulated Atmospheric Composition Mars Simulated Solar Spectrum Mars Diurnal Cycle Experimental Layout

€ Quartz tubes € ~1.0 gram regolith with ~3.0 cm depth profile y Subsampled at 1.0 cm depth profiles € 100 ppm of L-Asp, L-Glu, L- Ala, L-Val and Gly € Three sample categories y Mars conditions with UV y Mars conditions w/o UV y Controls at room temp and RH € Triplicate samples removed at 0, 10, 20, 30 and 40 days. Results

€ Acid hydrolysis, desalting, separation via HPLC as their OPA/NAC derivatives with UV detection

Retention Time € Rapid drop in the top of UV irradiated samples (red) y Small change in middle and bottom profiles until T=3 € Dark samples (blue) show minimal/no change at T=1 and increase with depth to plateau near -100 ppm; largest values at bottom. € Control samples (green) show minimal loss in the bottom layer until after T=2; maximum loss occurring in the top and middle layers. -kt Nt=N0 e

€ First order kinetics € Obvious trends in oxidation rate data; y UV samples show top down decrease y Dark samples show bottom up decrease y Controls show rate constant fairly independent; maybe increase in middle € Oxidation Rates Converge as they Approach Bottom; Similar Oxidation Mechanism Below the Top Centimeter? Conclusions

€ Data indicates multiple oxidation mechanisms y Photochemical oxidation in upper cm of UV sample ○ Only accounts for irradiation of about 0.1% of surface area; the remaining amount must be something else y Water increases rates of oxidation several orders of magnitude ○ Oxide radicals (Yen, 2000); peroxides (Bullock, 1994); hydroxide radicals (Benner, 2000) through metal leaching € So increased water increased oxidation! € Oxidation mechanisms that are controlled at depth by the rate of diffusion of water through the sample Dark Samples •Low temp; water in regolith freezes UV •Upper and middle Samples layers rapidly •Higher Temp sublimate; re-saturate (radiative heat) with time with •Water in regolith downward diffusion rapidly vaporizes away Control •UV in the upper layer Samples rapidly oxidizes organics •MUCH higher temp; •Diffusion of rapid diffusion and water/peroxides exchange of water through regolith with between regolith and time atmosphere from all depths Conclusions

€ A two part oxidation mechanism y A photolytic component in UV irradiated samples gives rise to rapid oxidation y With time and in a depth dependent manner, the diffusion of water and/or products from water photolysis diffusion through the regolith y Increased oxidation of the Martian regolith is due to the interaction of even minor amounts of water with minerals on the Martian surface € Missions designed to search for organic carbon/signs of life on Mars must sample from below this diffusion boundary! Acknowledgements

€ Indiana Princeton Tennessee Institute y Lisa Pratt € TechShot Laboratories of Greenville, IN € Collaborators from several universities y , Princeton y Rocco Mancinelli, SETI y Lynn Rothschild, NASA Ames y Susan Pfiffner, Tennessee y Lyle White, McGill University y Gaetan Borgonie, University of Ghent y Ruth Bryant, Albert Einstein School of Medicine € Indiana Space Grant References

€ Benner, S. A, et al. 2000. PNAS. 97, 2425-2430. € Biemann, K., et al. 1977. J. Geophys. Res. 82, 4641- 4658. € Bullock, M. A.,et al. 1994. Icarus. 107, 142-154. € Chun, S. F. S., et al. 1978. Nature. 274, 875-876. € Garry, J. R. C., et al. 2006. MAPS. 41, 391-405. € Kminek, G., Bada, J. L., 2006. EPSL. 245, 1-5. € McDonald, G. D., et al. 1998. Icarus. 132, 170-175. € Mumma, M. J., et al. 2009. Science. 1041-1045. € Yen, A. S., et al. 2000. Science. 289, 1909-1912. € Zent, A. P. McKay, C. P., 1994. Icarus. 108, 146- 157.