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Tectonics, volcanism, and climate on Venus may be strongly coupled. Large excursions in surface temperature predicted to follow a global or near-global volcanic event diffuse into the interior and introduce thermal stresses of a magnitude sufficient to influence widespread tectonic deformation. This sequence of events accounts for the timing and many of the characteristics of deformation in the ridged plains of Venus, the most widely preserved volcanic terrain on the planet.

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We report on laboratory experiments which simulate the breakdown of organic compounds under Martian surface conditions. Chambers containing Mars-analog soil mixed with the amino acid glycine were evacuated and filled to 100 mbar pressure with a Martian atmosphere gas mixture and then irradiated with a broad spectrum Xe lamp. Headspace gases were periodically withdrawn and analyzed via gas chromatography for the presence of organic gases expected to be decomposition products of the glycine. The quantum efficiency for the decomposition of glycine by light at wavelengths from 2000 to 2400 angstroms was measured to be 1.46 +/- 1.0 x 10(-6) molecules/photon. Scaled to Mars, this represents an organic destruction rate of 2.24 +/- 1.2 x 10(-4) g of C m-2 yr-1. We compare this degradation rate with the rate that organic compounds are brought to Mars as a result of meteoritic infall to show that organic compounds are destroyed on Mars at rates far exceeding the rate that they are deposited by meteorites. Thus the fact that no organic compounds were found on Mars by the Viking Lander Gas Chromatograph Mass Spectrometer experiment can be explained without invoking the presence of strong oxidants in the surface soils. The organic destruction rate may be considered as an upper bound for the globally averaged biomass production rate of extant organisms at the surface of Mars. This upper bound is comparable to the slow growing cryptoendolithic microbial communities found in dry Antarctica deserts. Finally, comparing these organic destruction rates to recently reported experiments on the stability of carbonate on the surface of Mars, we find that organic compounds may currently be more stable than calcite.

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The Viking Gas Chromatograph Mass Spectrometer failed to detect organic compounds on Mars, and both the Viking Labeled Release and the Viking Gas Exchange experiments indicated a reactive soil surface. These results have led to the widespread belief that there are oxidants in the martian soil. Since H2O2 is produced by photochemical processes in the atmosphere of Mars, and has been shown in the laboratory to reproduce closely the Viking LR results, it is a likely candidate for a martian soil oxidant. Here, we report on the results of a coupled soil/atmosphere transport model for H2O2 on Mars. Upon diffusing into the soil, its concentration is determined by the extent to which it is adsorbed and by the rate at which it is catalytically destroyed. An analytical model for calculating the distribution of H2O2 in the martian atmosphere and soil is developed. The concentration of H2O2 in the soil is shown to go to zero at a finite depth, a consequence of the nonlinear soil diffusion equation. The model is parameterized in terms of an unknown quantity, the lifetime of H2O2 against heterogeneous catalytic destruction in the soil. Calculated concentrations are compared with a H2O2 concentration of 30 nmoles/cm3, inferred from the Viking Labeled Release experiment. A significant result of this model is that for a wide range of H2O2 lifetimes (up to 10(5) years), the extinction depth was found to be less than 3 m. The maximum possible concentration in the top 4 cm is calculated to be approximately 240 nmoles/cm3, achieved with lifetimes of greater than 1000 years. Concentrations higher than 30 nmoles/cm3 require lifetimes of greater than 4.3 terrestrial years. For a wide range of H2O2 lifetimes, it was found that the atmospheric concentration is only weakly coupled with soil loss processes. Losses to the soil become significant only when lifetimes are less than a few hours. If there are depths below which H2O2 is not transported, it is plausible that organic compounds, protected from an oxidizing environment, may still exist. They would have been deposited by meteors, or be the organic remains of past life.

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