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Because of mass and power constraints in spacecraft, plant growth units designed for spaceflight have limited volume and low photosynthetic photon flux (PPF). Sufficient lighting and nutrient delivery are basic challenges to the success of supporting long-term plant growth in space. At the Kennedy Space Center, plant lighting and nutrient delivery hardware currently under NASA-sponsored development are being evaluated to define some of the fundamental issues associated with producing different fresh salad crops. Lettuce crops performed well under all nutrient delivery systems and lighting sources tested. Spinach and radish yields were lower in the presence of zeoponic media (using an ASTROCULTURE™ root tray) relative to plant grown in conventional NFT systems. Within each nutrient delivery system, yields of salad crops under red LEDs + blue light were similar to those crops grown under conventional white light.

The PESTO (Photosynthesis Experiment and System Testing and Operation) spaceflight experiment is designed to directly measure gas exchange of developing stands of wheat (Triticum aestivum L.) on the International Space Station (ISS). Gas exchange measurements will characterize photosynthesis and transpiration in microgravity at different stages of development. The Biomass Production System (BPS), a double middeck-sized plant growth will be the plant growth hardware used to support this experiment on-board ISS. This report presents results from a 10-day functional test of PESTO protocols in the BPS. Wheat canopy CO2 assimilation rate for 14-24 day-old plants grown in the BPS chambers was 6-7 μmol m-2 s-1 during this test. Plant responses to CO2 and photosynthetic photon flux (PPF) response curves were obtained at different stages of development by altering CO2 and light conditions.

The objectives of these experiments were two fold: 1) to determine if accepted tissue fixation procedures can be adapted for long-term storage on-board the International Space Station (ISS) and 2) to test whether they are suitable for KSC Fixation Tubes (KFTs). Three tissue fixation parameters were tested: time, temperature and sample size.Fixation time:samples are normally fixed from several minutes to several hours, but because of the duration of the UF-1 mission to ISS, the tissue will be in fixative for up to 3 months. Super dwarf wheat tissue samples were fixed in either FAA (a fixative normally used for storage of plant tissues) or a glutaraldehyde-based fixative and stored for 100 days.

The development of a spaceflight-rated Porous Tube Insert Module (PTIM) nutrient delivery tray has facilitated a series of studies evaluating various aspects of water and nutrient delivery to plants as they would be cultivated in space. We report here on our first experiment using the PTIM with a software-driven feedback moisture sensor control strategy for maintaining root zone wetness level set-points. One-day-old wheat seedlings (Tritium aestivum cv Apogee; N=15) were inserted into each of three Substrate Compartments (SCs) pre-packed with 0.25–1 mm Profile™ substrate and maintained at root zone relative water content levels of 70, 80 and 90%. The SCs contained a bottom-situated porous tube around which a capillary mat was wrapped. Three Porous Tubes were planted using similar protocols (but without the substrate) and also maintained at these three moisture level set-points. Half-strength modified Hoagland’s nutrient solution was used to supply water and nutrients.

The chemical specificity of several adsorbents, capable of being recycled by thermal desorption, was determined using volatile organic compounds (VOCs) found in ISS cabin air. These VOC adsorbents will be used to design a reusable filter to control ethylene in plant growth chambers and other STS/ISS biological payloads. A reusable filter to remove plant-produced ethylene from plant growth chambers could help minimize the mass and power use of plant flight hardware. Spaceflight-rated plant growth chambers employ either passive or active catalytic scrubbers for maintaining acceptable levels of VOCs. Passive systems require consumables, while active systems require power and their performance can be degraded in high humidity environments. Each adsorbent was loaded with known amounts of VOCs at a known flow rate. The filtering capacity and chemical specificity of each compound was determined from measurements pre- and post-filter VOC concentration.

With the installation of the Water Recovery System (WRS) during mission STS-126 in 2008, the International Space Station (ISS) added the capability to recover clean water for reuse from crewmember urine and atmospheric humidity condensate, including EVA (Extravehicular Activity) wastes. The ability to collect, store and process these waste streams is required to increase potable water recovery and support the ISS crew augmentation planned for 2009. During ground testing of the Urine Processing Assembly (UPA), one of two primary component subsystems that comprise the WRS, significant fouling was repeatedly observed in stored urine pretreated with 0.56% of chromium trioxide and sulfuric acid. During initial observation, presumptive microbiological growth clogged and damaged flight-rated hardware under test as part of a risk-mitigation Flight Experiment (FE).

This work describes the microbiological assessment and materials compatibility of a silver-based biocide as an alternative to iodine for the Crew Exploration Vehicle (CEV) and future spacecraft potable water systems. In addition to physical and operational anti-microbial counter-measures, the prevention of microbial growth, biofilm formation, and microbiologically induced corrosion in water distribution and storage systems requires maintenance of a biologically-effective, residual biocide concentration in solution and on the wetted surfaces of the system. Because of the potential for biocide depletion in water distribution systems and the development of acquired biocide resistance within microbial populations, even sterile water with residual biocide may, over time, support the growth and/or proliferation of bacteria that pose a risk to crew health and environmental systems.