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	<title>bioregenerative life support &#8211; Science</title>
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	<title>bioregenerative life support &#8211; Science</title>
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		<title>Hydrogel Granules Could Slash Water Use for Growing Food in Space</title>
		<link>https://scienmag.com/hydrogel-granules-could-slash-water-use-for-growing-food-in-space/</link>
		
		<dc:creator><![CDATA[Alan Morgan]]></dc:creator>
		<pubDate>Thu, 15 Oct 2026 13:51:19 +0000</pubDate>
				<category><![CDATA[Science News]]></category>
		<category><![CDATA[Technology and Engineering]]></category>
		<category><![CDATA[Advanced Plant Habitat]]></category>
		<category><![CDATA[arcillite]]></category>
		<category><![CDATA[bioregenerative life support]]></category>
		<category><![CDATA[hydrogel properties for space]]></category>
		<category><![CDATA[hydrogel versus clay in space]]></category>
		<category><![CDATA[hydrogel water efficiency]]></category>
		<category><![CDATA[hydrogels]]></category>
		<category><![CDATA[International Space Station]]></category>
		<category><![CDATA[ionomics]]></category>
		<category><![CDATA[microgravity plant growth]]></category>
		<category><![CDATA[photosystem II]]></category>
		<category><![CDATA[plant growth in space missions]]></category>
		<category><![CDATA[polyacrylamide]]></category>
		<category><![CDATA[radish]]></category>
		<category><![CDATA[Raphanus sativus]]></category>
		<category><![CDATA[space agriculture]]></category>
		<category><![CDATA[space farming substrates]]></category>
		<category><![CDATA[space station crop cultivation]]></category>
		<category><![CDATA[sustainable space farming solutions]]></category>
		<category><![CDATA[synthetic polymer granules]]></category>
		<category><![CDATA[water conservation in space]]></category>
		<category><![CDATA[water recycling in space agriculture]]></category>
		<category><![CDATA[water-use efficiency]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=275244</guid>

					<description><![CDATA[Radishes grown in polyacrylamide hydrogel granules matched the yields of plants raised in the clay substrate used on the International Space Station while requiring significantly less water, positioning hydrogels as a promising foundation for space agriculture.]]></description>
										<content:encoded><![CDATA[<p>Radishes grown in synthetic polymer granules produced the same leaf and bulb biomass as those grown in the clay substrate currently used aboard the International Space Station, but required significantly less water, according to a new study published in Frontiers in Space Technologies. The finding, from researchers Nicholas Miklave and Karl Hasenstein at the University of Louisiana at Lafayette, suggests that hydrogels such as polyacrylamide could outperform the calcined montmorillonite clay known as arcillite in the water-limited environments of long-duration spaceflight, where every liter of water must be recycled, stored, or launched at enormous cost.</p>
<p>Arcillite is the substrate of choice in NASA&#8217;s Advanced Plant Habitat, where porous tubes deliver water into a bed of 1 to 2 millimeter clay particles that distribute moisture through the root zone while maintaining the air-filled pores that roots need to avoid hypoxia. That particle size window is critical in microgravity, where the absence of buoyancy-driven drainage makes water behavior in porous media fundamentally different from that on Earth. Yet arcillite carries a persistent liability: as a natural, calcined clay product, its mineral composition varies considerably between batches, and excess soluble minerals can stunt germination and growth when the substrate is not properly conditioned.</p>
<p>Hydrogels, by contrast, are manufactured materials whose chemical and physical properties can be engineered with precision. Terrestrial agriculture has long used them as soil amendments to improve water retention in arid regions and clay-heavy soils, and they can be formulated to slowly release fertilizers and other agrochemicals. Because they can be packaged dry and rehydrated on demand, hydrogels also promise dramatic reductions in launch mass and storage volume compared with dense ceramic granules. The open question was whether these benefits persist when a hydrogel serves as the sole growth substrate rather than a minor additive.</p>
<p>To find out, the team synthesized polyacrylamide granules by polymerizing droplets of acrylamide solution in hot silicone oil, then washing and drying the resulting beads. They compared these against two distinct batches of arcillite, one acquired in 2019 and one in 2024, both sifted to the flight-standard 1 to 2 millimeter fraction. Root modules modeled on the Advanced Plant Habitat science carriers were filled with either 1,300 grams of arcillite or just 100 grams of dry polyacrylamide, infused with identical half-strength Murashige and Skoog nutrient solution, and planted with Cherry Belle radish seeds, a cultivar with an extensive history in space biology research.</p>
<p>Over three sequential grow-outs, the researchers tracked daily water loss gravimetrically, harvested plants at 28 days, and measured photosystem II efficiency, leaf mass per area, and the full elemental composition of leaves and bulbs using inductively coupled plasma optical emission spectroscopy. The results exposed a striking inconsistency between the two arcillite batches. Plants grown in the 2024 batch produced significantly less leaf tissue and smaller bulbs, consumed only 2.1 liters of water per container compared with 4.6 liters in the 2019 batch, and showed altered photosystem II behavior. Chemical analysis revealed that the poorly performing batch released substantially more soluble calcium, magnesium, selenium, and sulfur into the root zone.</p>
<p>The photosynthetic data provided a physiological signature of that stress. In plants grown in the 2019 arcillite and in polyacrylamide, the quantum yield of photosystem II declined by roughly 3 to 4 percent as leaves matured, a normal developmental pattern. In the 2024 arcillite, that age-related decline vanished entirely, a response the authors associate with stress, since drought, salinity, and nutrient toxicity are all known to disrupt the typical relationship between leaf age and photosynthetic efficiency. Excess calcium, in particular, has been linked in prior studies to reduced growth and impaired chlorophyll fluorescence, and the ionomic analysis suggested that high calcium and copper in the 2024 batch may have antagonized the uptake of manganese, iron, and other essential cations.</p>
<p>Against the well-behaved 2019 arcillite, polyacrylamide held its own on yield while winning decisively on water. There was no difference in leaf or bulb biomass or in photosystem II efficiency between the two substrates, but radishes in the hydrogel consumed significantly less water overall, translating into higher water use efficiency, the ratio of fresh biomass produced to water consumed. Because the closed containers lost no water to percolation or runoff, the authors attribute the advantage not to superior water retention but possibly to changes in substrate matric potential that alter how plants access and transpire water. Notably, evapotranspiration rates were identical across all substrates during the first 12 days, when substrate evaporation dominates, meaning the divergence emerged only once transpiration took over.</p>
<p>The study also uncovered an unexpected bonus: polyacrylamide appears to supply nitrogen. Leaf mass per area, a trait strongly correlated with leaf nitrogen content and photosynthetic capacity, was highest in hydrogel-grown plants during the first grow-out and declined with substrate reuse. The authors propose that acidic root exudates hydrolyzed some of the polymer&#8217;s amide side chains, releasing ammonium as a bioavailable nitrogen source during the first cropping cycle. The granules swelled about 2.5-fold when hydrated, and their water holding capacity actually increased after the first grow-out when hydrated with pure water, though it remained stable in nutrient solution, indicating reasonable durability across repeated use.</p>
<p>For mission planners, the implications extend beyond the growth chamber. Hydrogels can be copolymerized or infused with growth regulators, vitamins, and amino acids tailored to specific crops, and their ion exchange capabilities could help strip toxic perchlorates from Martian regolith, a known barrier to germination there. Spent hydrogel substrate might even be repurposed as organic matter to seed soil formation in lunar or Martian greenhouses, or engineered into super-hygroscopic forms that scavenge humidity from cabin air to manage water in microgravity. The authors caution that open questions remain, including long-term reusability, hydraulic behavior under reduced gravity, the fate of polymer degradation products in closed-loop life support systems, and best practices for sterilization. They also suggest that hybrid substrates combining arcillite or regolith with hydrogel granules may ultimately deliver benefits neither material achieves alone. But the core message is clear: a synthetic, uniform, lightweight substrate that matches the yield of flight-proven clay while cutting water demand could reshape how future crews grow food on the way to Mars.</p>
<p><strong>Subject of Research:</strong> Comparison of polyacrylamide hydrogel and arcillite clay as plant growth substrates for space agriculture</p>
<p><strong>Article Title:</strong> A comparison between polyacrylamide and arcillite granules as substrates for space agriculture</p>
<p><strong>Article References:</strong> Miklave, N. M., &amp; Hasenstein, K. H. (2026). A comparison between polyacrylamide and arcillite granules as substrates for space agriculture. <em>Frontiers in Space Technologies, 7</em>, Article 1899542. <a href="https://doi.org/10.3389/frspt.2026.1899542" rel="noopener noreferrer">https://doi.org/10.3389/frspt.2026.1899542</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3389/frspt.2026.1899542" rel="noopener noreferrer">10.3389/frspt.2026.1899542</a></p>
<p><strong>Keywords:</strong> space agriculture, polyacrylamide, arcillite, hydrogels, radish, Raphanus sativus, water use efficiency, International Space Station, Advanced Plant Habitat, photosystem II, ionomics, bioregenerative life support</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">275244</post-id>	</item>
		<item>
		<title>Plant Cell Walls Hold Firm Under Everest-Level Low Pressure, Study Finds</title>
		<link>https://scienmag.com/plant-cell-walls-hold-firm-under-everest-level-low-pressure-study-finds/</link>
		
		<dc:creator><![CDATA[Alan Morgan]]></dc:creator>
		<pubDate>Tue, 06 Oct 2026 18:21:01 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[Arabidopsis thaliana]]></category>
		<category><![CDATA[bioregenerative life support]]></category>
		<category><![CDATA[bioregenerative life support systems]]></category>
		<category><![CDATA[Everest-level atmospheric pressure resistance]]></category>
		<category><![CDATA[genetically stable plant structures in space]]></category>
		<category><![CDATA[glycomics]]></category>
		<category><![CDATA[HPAEC-PAD]]></category>
		<category><![CDATA[hypobaria]]></category>
		<category><![CDATA[hypoxia]]></category>
		<category><![CDATA[impact of reduced pressure on plant tissues]]></category>
		<category><![CDATA[low-pressure space environments]]></category>
		<category><![CDATA[matrix polysaccharides]]></category>
		<category><![CDATA[NASA-funded plant biology research]]></category>
		<category><![CDATA[PDC1]]></category>
		<category><![CDATA[plant biochemical response to low pressure]]></category>
		<category><![CDATA[plant cell wall]]></category>
		<category><![CDATA[plant cell wall biomechanics]]></category>
		<category><![CDATA[space agriculture]]></category>
		<category><![CDATA[space agriculture resilience]]></category>
		<category><![CDATA[space farming sustainability]]></category>
		<category><![CDATA[space mission habitat safety]]></category>
		<category><![CDATA[spacecraft habitat design]]></category>
		<category><![CDATA[spaceflight]]></category>
		<category><![CDATA[SWEET11]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=242179</guid>

					<description><![CDATA[New research shows that Arabidopsis cell wall matrix polysaccharides remain biochemically unchanged under hypobaric pressures as low as 33 kilopascals, despite growth reductions and stress-related gene expression.]]></description>
										<content:encoded><![CDATA[<p>As space agencies sketch out plans for long-duration missions to the Moon and Mars, one engineering problem keeps surfacing: spacecraft cabins filled with sea-level atmospheric pressure are heavy, leak-prone, and wasteful. Running habitats at reduced pressure would ease structural loads, make spacewalks safer by reducing the risk of decompression sickness, and conserve precious gases. But lowered cabin pressure would also mean lowered pressure for the crops that future crews hope to grow inside bioregenerative life support systems. A new study published in Plant Direct has now delivered some of the most direct biochemical evidence yet that a key part of plant anatomy can withstand those alien conditions remarkably well. Researchers found that the matrix polysaccharides of the plant cell wall, the structural scaffolding that gives tissues their shape and flexibility, remain essentially unchanged even when seedlings are exposed to atmospheric pressures as low as those found at the summit of Mount Everest.</p>
<p>The research team, funded by NASA and the USDA National Institute of Food and Agriculture, set out to test a long-standing hypothesis in space plant biology. Previous transcriptomic studies had shown that when plants are placed in low-pressure environments, hundreds of genes change their expression, including genes involved in cell wall biosynthesis and sugar transport. Genes encoding galacturonosyltransferases such as GAUT7, which build pectin backbones, and xyloglucan endo-transglycosylase/hydrolases such as XTH16, which remodel hemicellulose, were differentially expressed, as were sugar transporter genes of the SWEET family. On paper, that molecular activity suggested the cell wall might be physically altered by hypobaria. But gene expression is only a proxy. Until now, no one had directly measured the actual biochemical composition of cell walls from plants grown under low pressure, leaving a gap between molecular hints and material reality.</p>
<p>To close that gap, the researchers grew four genotypes of Arabidopsis thaliana, the standard workhorse of plant genetics: the wild-type accessions Columbia (Col-0) and Wassilewskija (Ws), plus two knockout mutants, pdc1 and sweet11, each disrupted in a gene previously implicated in the hypobaric response. The seedlings were raised vertically in sterile culture for ten days under constant light at 23 degrees Celsius, then subjected to three-day pressure treatments in a trio of interconnected polycarbonate chambers with a combined interior volume of roughly 7,500 cubic centimeters. A vacuum controller held the chambers at target pressures of 75, 50, or 33 kilopascals, with 98 kilopascals serving as the sea-level control. Because the atmospheric composition was not artificially manipulated, reducing total pressure also reduced the partial pressure of oxygen, creating combined hypobaric-hypoxic conditions with oxygen partial pressures of approximately 16, 10.7, and 7 kilopascals respectively.</p>
<p>The choice of 33 kilopascals was deliberate and dramatic. That figure approximates the total atmospheric pressure at the peak of Mount Everest, some 8,847 meters above sea level, and sits well below the roughly 47 kilopascals that appears to mark the natural altitudinal limit of terrestrial plant life. It also falls far outside the 55 to 65 kilopascals proposed for future spacecraft cabins. In other words, the seedlings were pushed beyond anything in the evolutionary experience of lowland crop plants, into a regime that exists on Earth only at the planet&#8217;s most extreme elevations, and even there only briefly and in combination with cold, drought, and intense ultraviolet radiation.</p>
<p>The morphological results were sobering but expected. Seedlings grown at 33 kilopascals were visibly smaller and stunted compared with controls, and their shoots showed statistically significant reductions in fresh weight. This aligns with a broader literature on hypobaric plant physiology: lettuce grown at 25 kilopascals for ten days lost roughly 46 percent of its dry leaf weight in one study, and other work across monocots and dicots has documented mixed but recurring growth penalties under low pressure. The picture is complicated by the fact that hypobaria and hypoxia travel together when atmospheric composition is uncorrected, and previous experiments have shown that drought-like stress responses can be triggered by low pressure even when water is freely available. Disentangling those components remains an active area of research.</p>
<p>But the biochemical story turned out very differently. Using a technique called high-performance anion-exchange chromatography with pulsed amperometric detection, or HPAEC-PAD, the team quantified nine cell wall monosaccharides, including fucose, rhamnose, arabinose, galactose, glucose, xylose, mannose, galacturonic acid, and glucuronic acid, in both root and shoot tissues. The procedure involved extracting the alcohol insoluble residue from roughly 100 milligrams of frozen tissue, hydrolyzing the wall polysaccharides with 2 molar trifluoroacetic acid at 120 degrees Celsius for 90 minutes, and normalizing the released sugars against an internal ribose standard and an external calibration curve. The result across three independent experimental repetitions was strikingly uniform: no consistent differences in matrix polysaccharide composition attributable to pressure treatment, in either tissue type, at any of the tested pressures.</p>
<p>Equally notable was the behavior of the mutants. The sweet11 knockout was of particular interest because earlier work using Fourier transform infrared spectroscopy had suggested that disrupting SWEET11 and its relative SWEET12 could alter the abundance of acidic pectins and rhamnogalacturonans in the wall. Yet in this study, sweet11 showed no consistent differences in monosaccharide composition from its Col-0 wild type or from the Ws ecotype, at control pressure or under any hypobaric treatment. The pdc1 mutant, chosen because pyruvate decarboxylase 1 is reliably induced under both normoxic and hypoxic hypobaria and plays a central role in low-oxygen responses, likewise failed to diverge from wild type. Whatever roles these genes play in the hypobaric stress response, they do not appear to be required for maintaining the bulk monosaccharide composition of the cell wall matrix.</p>
<p>The authors are careful about what this resilience does and does not mean. The technique measures the overall abundance of constituent monosaccharides, not the fine structural organization of the polysaccharides, their degree of methylesterification or acetylation, or their cross-linking architecture. Subtle chemical modifications that would not show up in a monosaccharide profile remain unexplored. The experiments also covered only three days of exposure in young seedlings, so the effects of long-term hypobaria spanning a full life cycle, or of plants germinated and grown entirely under low pressure, are still unknown. And the fresh weight penalty at 33 kilopascals shows that resilience at the biochemical level does not translate into unimpaired growth under the most severe conditions tested.</p>
<p>Nevertheless, the study represents a genuine first: the earliest application of glycomic techniques to the question of how hypoxic hypobaric environments affect plant cell wall composition at the monosaccharide level. Its central conclusion, that the cell wall matrix of young Arabidopsis seedlings is resilient to hypobaric exposure, offers cautious encouragement for the designers of extraterrestrial greenhouses. The transcriptomic alarm bells that ring when plants encounter low pressure, it turns out, do not necessarily signal structural damage to the wall itself; they may reflect regulatory adjustments that successfully preserve wall composition. For mission planners weighing the trade-offs between cabin pressure and crop performance, that distinction matters. If the structural fabric of plant tissues holds steady at pressures relevant to proposed habitats, the engineering case for low-pressure agriculture in space grows stronger, even as the questions about long-term adaptation, wall architecture, and growth under sustained hypobaria keep the field busy for years to come.</p>
<p><strong>Subject of Research:</strong> The biochemical resilience of plant cell wall matrix polysaccharides under hypobaric stress relevant to space agriculture</p>
<p><strong>Article Title:</strong> Hypobaric Resilience of Matrix Polysaccharide Biosynthesis in Plants</p>
<p><strong>Article References:</strong> Strickland, H. F., Jacobson, T., Smith, G., Voiniciuc, C., Schuerger, A. C., Paul, A.-L., &amp; Ferl, R. (2026). Hypobaric Resilience of Matrix Polysaccharide Biosynthesis in Plants. <em>Plant Direct, 10</em>(10), Article e70190. <a href="https://doi.org/10.1002/pld3.70190" rel="noopener noreferrer">https://doi.org/10.1002/pld3.70190</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1002/pld3.70190" rel="noopener noreferrer">10.1002/pld3.70190</a></p>
<p><strong>Keywords:</strong> hypobaria, plant cell wall, Arabidopsis thaliana, space agriculture, bioregenerative life support, matrix polysaccharides, HPAEC-PAD, hypoxia, SWEET11, PDC1, spaceflight, glycomics</p>
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