Task Progress:
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During the reporting period we made significant progress on the stated objectives of this project. As our hypothesis is that reactive oxygen species (ROS) initiates the chemical reactions that lead to the toxicity of regolith, we began by exploring ROS production in simulated regolith. Our first objective was to establish laboratory methods to detect and quantify reactive oxygen species. We effectively adapted published methods into a high-throughput quantitative method. Based on this data, we showed grinding regolith in a mortal and pestle, a known mechanism to activate ROS, increased the ROS signal 5-fold over unground samples. We altered the chemical composition of the regolith by adding iron and chromium oxides to more closely mimic samples from the Apollo missions. The addition of these compounds did not significantly alter the production of ROS. Additionally, we tested whether storing the ground regolith under an inert gas would prevent loss of ROS (in normal air, ROS naturally deactivates over the course of a few hours). Ground regolith retained only 10% of its ROS producing activity after one week, suggesting the use of fresh ground regolith is advisable for future experiments.
Manual grinding of regolith approximates the decomposition of regolith pieces due to space weathering and micrometeor impacts. However, it’s a low energy approximation of these phenomena. We have begun a collaboration with the Vertical Gun Range at NASA Ames Research Center where we aim to use high velocity projectiles to better simulate the energy of micrometeors and generate more accurate simulants.
Next, we performed initial experiments on the microorganism we aim to use for phycoremediation: Spirulina. To this end, we first built a custom, water-cooled experimental setup to determine oxygen production by Spirulina when it is performing photosynthesis. The water-cooled setup prevents drift in the oxygen sensors due to temperature fluctuations as the light gets brighter. The resulting data was of high quality and provided the necessary experimental parameters for follow-on experiments. Finally, we verified methods to separate Spirulina from the regolith for down-stream analysis. We hypothesized that phototaxis – the ability of photosynthetic microorganisms to migrate towards a light source – could be used to separate microbes from the soil. Indeed, using targeting lighting, the Spirulina cells migrated away from the regolith towards the light, and could be isolated for additional testing. Taken together, all preliminary experiments have been completed and we are prepared to perform plant growth experiments in the coming months.
Looking forward, we will take these methods forward to accomplish the remaining objectives of this project. We anticipate being able to complete all tasks by the end of 2025.
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