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	<title>biomass allocation &#8211; Science</title>
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	<title>biomass allocation &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>Silicon and mycorrhizal fungi shape maize drought response differently</title>
		<link>https://scienmag.com/silicon-and-mycorrhizal-fungi-shape-maize-drought-response-differently/</link>
		
		<dc:creator><![CDATA[Roger Howard]]></dc:creator>
		<pubDate>Thu, 22 Oct 2026 00:30:21 +0000</pubDate>
				<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[arbuscular]]></category>
		<category><![CDATA[arbuscular mycorrhizal fungi]]></category>
		<category><![CDATA[biomass allocation]]></category>
		<category><![CDATA[Biomass allocation in drought conditions]]></category>
		<category><![CDATA[Combined silicon and fungi application in drought stress]]></category>
		<category><![CDATA[controlled experiment]]></category>
		<category><![CDATA[Drought resilience mechanisms in maize]]></category>
		<category><![CDATA[drought stress]]></category>
		<category><![CDATA[Effects of silicon on stem thickness]]></category>
		<category><![CDATA[Experimental evaluation of plant drought responses]]></category>
		<category><![CDATA[fungi]]></category>
		<category><![CDATA[maize]]></category>
		<category><![CDATA[Maize drought tolerance]]></category>
		<category><![CDATA[mycorrhizal]]></category>
		<category><![CDATA[Mycorrhizal fungi influence on root biomass]]></category>
		<category><![CDATA[Plant morphological changes under drought]]></category>
		<category><![CDATA[plant water status]]></category>
		<category><![CDATA[Role of arbuscular mycorrhizal fungi in leaf area expansion]]></category>
		<category><![CDATA[root growth]]></category>
		<category><![CDATA[shoot biomass]]></category>
		<category><![CDATA[Short-term drought response in maize]]></category>
		<category><![CDATA[silicon]]></category>
		<category><![CDATA[Silicon effects on plant water content]]></category>
		<category><![CDATA[Water status measurement in drought-stressed maize]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=331247</guid>

					<description><![CDATA[A controlled experiment found that silicon and arbuscular mycorrhizal fungi produced distinct changes in water status, growth and biomass allocation in drought-stressed maize.]]></description>
										<content:encoded><![CDATA[<p>In an experiment on drought-stressed maize, silicon and arbuscular mycorrhizal fungi produced distinct changes in plant performance, with silicon associated with thicker stems and higher relative water content and fungal inoculation associated with larger leaves and greater root dry weight. After a seven-day drought imposed at the vegetative growth stage, silicon increased stem diameter to 15.17 millimeters and produced the highest relative water content, at 88.33%. Arbuscular mycorrhizal fungi increased leaf area to 88.41 square centimeters and root dry weight to 25.12 grams. Applying silicon and the fungi together produced the greatest shoot dry weight, reaching 99.10 grams.</p>
<p>The researchers evaluated silicon alone, arbuscular mycorrhizal fungi alone and the combined treatment in maize, <i>Zea mays</i>. Leaf water-status traits were measured immediately after the drought, while morphological and biomass traits were evaluated following a five-day recovery period after rewatering. This timing distinction is important because the water measurements and the growth responses were not all collected at the same stage. The study examined biomass allocation and plant water relations under controlled experimental conditions; it did not establish improvements in field yield, long-term drought resilience or production under sustained water limitation.</p>
<p>The clearest contrasts involved traits associated with different parts of the plant. Silicon was associated with greater stem diameter and maintained relative water content, whereas fungal inoculation was associated with larger leaf area and greater root dry weight. The combination supported greater shoot biomass, but this did not translate into a significant change in every measured characteristic. Root-to-shoot ratio, water saturation deficit and water uptake capacity were not significantly affected. The results therefore indicate that silicon and arbuscular mycorrhizal fungi altered selected components of maize performance rather than producing a uniform improvement across all biomass- and water-related traits.</p>
<p>Principal component analysis summarized associations among the biomass- and water-related traits and accounted for 61.5% of the total variation. The analysis identifies patterns linking plant form, resource allocation and water status, but it does not independently demonstrate an effect on crop yield. Collectively, the experiment shows that silicon and arbuscular mycorrhizal fungi can influence different aspects of maize performance during drought and subsequent recovery. The findings support further evaluation of these interventions for water-limited maize production, while the experimental scope leaves questions about field performance and longer-term benefits unresolved.</p>
<p><strong>Subject of Research:</strong> Effects of silicon and arbuscular mycorrhizal fungi on drought response and biomass allocation in maize</p>
<p><strong>Article Title:</strong> Silicon and arbuscular mycorrhizal fungi alter biomass partitioning and water-use traits in drought-stressed maize (Zea mays)</p>
<p><strong>Article References:</strong> Guanzon, I. M., Dolores, J. F. A. H., Dungo, L. P. P., Mariano, M. A. L., &amp; Vergara, C. J. E. (2026). Silicon and arbuscular mycorrhizal fungi alter biomass partitioning and water-use traits in drought-stressed maize (Zea mays). <em>Discover Sustainability</em>. <a href="https://doi.org/10.1007/s43621-026-04732-2" rel="noopener noreferrer">https://doi.org/10.1007/s43621-026-04732-2</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s43621-026-04732-2" rel="noopener noreferrer">10.1007/s43621-026-04732-2</a></p>
<p><strong>Keywords:</strong> maize, drought stress, silicon, arbuscular mycorrhizal fungi, biomass allocation, plant water status, root growth, shoot biomass, controlled experiment, arbuscular, mycorrhizal, fungi</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">331247</post-id>	</item>
		<item>
		<title>When Drought Strikes Late: Timing Holds the Key to Alpine Meadow Survival</title>
		<link>https://scienmag.com/when-drought-strikes-late-timing-holds-the-key-to-alpine-meadow-survival/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Sun, 11 Oct 2026 13:12:35 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[alpine meadow]]></category>
		<category><![CDATA[Alpine meadow drought resilience]]></category>
		<category><![CDATA[biomass allocation]]></category>
		<category><![CDATA[climate change]]></category>
		<category><![CDATA[climate change effects on alpine ecosystems]]></category>
		<category><![CDATA[drought timing]]></category>
		<category><![CDATA[effects of late-season drought on plant resource allocation]]></category>
		<category><![CDATA[extreme events]]></category>
		<category><![CDATA[grassland ecology]]></category>
		<category><![CDATA[high-altitude precipitation manipulation studies]]></category>
		<category><![CDATA[legacy effect]]></category>
		<category><![CDATA[long-term ecological experiments in high-altitude environments]]></category>
		<category><![CDATA[modeling grassland responses to climate variability]]></category>
		<category><![CDATA[plant biomass and community dynamics during drought periods]]></category>
		<category><![CDATA[plant plasticity]]></category>
		<category><![CDATA[precipitation manipulation]]></category>
		<category><![CDATA[Qinghai-Tibet Plateau]]></category>
		<category><![CDATA[Qinghai-Tibet Plateau ecosystem]]></category>
		<category><![CDATA[root architecture and drought memory]]></category>
		<category><![CDATA[root-to-shoot ratio]]></category>
		<category><![CDATA[seasonal drought stress in grasslands]]></category>
		<category><![CDATA[soil nitrogen]]></category>
		<category><![CDATA[soil physicochemical changes under drought conditions]]></category>
		<category><![CDATA[timing of drought impact on grassland plants]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=262290</guid>

					<description><![CDATA[A four-year rainout shelter experiment on the Qinghai-Tibet Plateau shows that late season drought shifts root-to-shoot allocation in alpine meadows far more strongly than early season drought, with sequential droughts producing powerful synergistic effects.]]></description>
										<content:encoded><![CDATA[<p>On the vast, windswept expanse of the Qinghai-Tibet Plateau, the question of when a drought arrives may matter as much as how severe it is. A new four-year field experiment, published in the journal Plant and Soil, reveals that extreme drought striking late in the growing season reshapes the way alpine meadow plants invest their resources far more dramatically than drought striking early in the season. The finding, drawn from one of the longest precipitation-manipulation studies ever conducted in this high-altitude ecosystem, carries sobering implications for how scientists model the fate of grasslands under a warming climate, and it offers a striking example of how the hidden architecture of roots can betray the memory of past stress.</p>
<p>The research team, led by Jiayu Xu and Biying Qiu of Henan University and Liaoning University together with colleagues, set up rainout shelters across an alpine meadow site on the plateau between 2021 and 2024. Using a two-factor randomized complete block design, they simulated extreme drought either early or late in the growing season, or in both windows sequentially, and then measured aboveground and belowground biomass, community characteristics, and soil physicochemical properties every year. The statistical toolkit was correspondingly rigorous: two-way repeated-measures analysis of variance to isolate treatment effects, structural equation modeling to trace causal pathways among biotic and abiotic variables, and linear regression to quantify correlations across the four years of data.</p>
<p>The headline result is deceptively simple but ecologically profound. Late season drought increased the ratio of root biomass to shoot biomass by 56 percent, compared with a 24 percent increase under early season drought. The root-to-shoot ratio is one of the most fundamental currencies in plant ecology, a measure of how a plant splits its carbon budget between the organs it needs to forage for water and nutrients below ground and the organs it needs to capture light and carbon dioxide above ground. A larger ratio typically signals a plant hedging its bets against water scarcity, building more root infrastructure to chase receding soil moisture at the expense of leafy growth.</p>
<p>Why would late season drought push plants to reallocate so much more aggressively than early season drought? The researchers traced the answer to a combination of legacy effects and constrained plasticity. Early season drought, they found, created a legacy by depleting shallow soil moisture and altering the physiological status of the plants, leaving them in a compromised state heading into the rest of the season. But it was the late season drought that limited the plants&#8217; capacity to respond plastically, because by that point in the season soil moisture, plant cover, and soil nitrogen availability had all been reduced. In other words, plants hit by drought late in the season face the stress with fewer resources and less time to reorganize their growth, forcing a stronger shift of biomass below ground.</p>
<p>Perhaps the most striking discovery, however, lies in what happens when both droughts occur in the same year. Early season and late season drought did not simply add their effects together; they showed a positive synergistic interaction. Early season drought alone increased the root-to-shoot ratio by 1.0 unit, but when it was followed by late season drought, that increase swelled to 6.4 units. A mirrored pattern appeared for late season drought, whose effect was likewise amplified when an early season drought had preceded it. The sequential double punch, in which an early drought primes the system and a late drought delivers the blow, produces allocation shifts far larger than either stress in isolation, a signature of compound extreme events that most climate models have yet to capture.</p>
<p>This synergy matters because climate change is not only making droughts more intense; it is shifting when they occur. Warming is altering the seasonal distribution of precipitation across the globe, and on the Qinghai-Tibet Plateau specifically, studies have documented changes in precipitation concentration, multi-type drought propagation, and amplified precipitation seasonality. Alpine meadows cover enormous areas of the plateau and underpin the livelihoods of pastoral communities, the water resources of major Asian rivers, and significant carbon stocks. If the timing of drought determines how these ecosystems restructure themselves, then projections that treat drought as a seasonally anonymous stressor may systematically misjudge future vegetation change, forage production, and carbon sequestration.</p>
<p>The structural equation modeling in the study helps explain the mechanism in more detail. By linking soil moisture, plant cover, and nitrogen availability to biomass allocation within a single causal framework, the analysis showed that late season drought constrains plant plasticity through multiple simultaneous pathways. Reduced soil moisture directly limits water uptake; reduced plant cover diminishes the photosynthetic machinery available to generate new biomass; and reduced soil nitrogen availability constrains the construction of new tissue, since nitrogen is a core building block of proteins and chlorophyll. A plant facing this triple constraint late in the season has little option but to favor roots, the organs that determine whether it can survive into the next year.</p>
<p>The findings also connect to a broader literature on drought legacy effects in grasslands. Previous work has shown that drought can alter soil respiration through root exudates, that high belowground bud abundance can speed ecosystem recovery, and that drought timing differentially affects aboveground and belowground productivity in mesic grasslands. What the new study adds is a quantified, multi-year demonstration from an alpine system that the sequence of droughts within a single season, not just their individual occurrence, governs the magnitude of allocation shifts. The amplification factor, from a 1.0-unit increase to a 6.4-unit increase in the root-to-shoot ratio, gives modelers a concrete parameter to test against.</p>
<p>For the carbon cycle, the implications run deep. Roots are the primary conduit through which photosynthesized carbon enters the soil, and shifts in allocation toward belowground biomass can change rhizodeposition, soil organic matter formation, and ultimately whether an ecosystem acts as a carbon sink or source. If late season droughts become more frequent under future precipitation regimes, alpine meadows could channel progressively more of their carbon underground, altering soil carbon storage in ways that depend critically on drought timing. The authors argue that their results provide empirical evidence for improving predictions of alpine meadow ecosystem responses to future climate scenarios, and the four-year duration of the experiment lends that claim unusual weight for a field manipulation at this altitude.</p>
<p>The study, published on 8 September 2026 in Plant and Soil and supported by the National Natural Science Foundation of China, arrives at a moment when ecologists are increasingly recognizing that the impacts of climate extremes depend crucially on their timing. As one of the first experiments to disentangle early and late season drought effects on biomass allocation in an alpine meadow over multiple consecutive years, it delivers a clear message: to understand how grasslands will weather the climate of the coming decades, scientists must stop asking only how much rain falls, and start asking precisely when it fails to fall. On the roof of the world, the calendar of drought may decide the fate of the meadows below.</p>
<p><strong>Subject of Research:</strong> Effects of drought timing on plant biomass allocation in alpine meadows on the Qinghai-Tibet Plateau</p>
<p><strong>Article Title:</strong> Late season drought has stronger effects on plant biomass allocation than early season drought in alpine meadows</p>
<p><strong>Article References:</strong> Xu, J., Qiu, B., Yang, J., Sun, Y., Guo, M., Yang, Z., Miao, R., &amp; Li, G. (2026). Late season drought has stronger effects on plant biomass allocation than early season drought in alpine meadows. <em>Plant and Soil</em>. <a href="https://doi.org/10.1007/s11104-026-09068-4" rel="noopener noreferrer">https://doi.org/10.1007/s11104-026-09068-4</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s11104-026-09068-4" rel="noopener noreferrer">10.1007/s11104-026-09068-4</a></p>
<p><strong>Keywords:</strong> drought timing, biomass allocation, root-to-shoot ratio, alpine meadow, Qinghai-Tibet Plateau, legacy effect, precipitation manipulation, climate change, grassland ecology, plant plasticity, soil nitrogen, extreme events</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">262290</post-id>	</item>
		<item>
		<title>Winning Microbe: Sinorhizobium fredii Outperforms Rivals in Cowpea Nodulation Trial</title>
		<link>https://scienmag.com/winning-microbe-sinorhizobium-fredii-outperforms-rivals-in-cowpea-nodulation-trial/</link>
		
		<dc:creator><![CDATA[Alan Morgan]]></dc:creator>
		<pubDate>Sat, 03 Oct 2026 20:51:03 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[biofertilizer]]></category>
		<category><![CDATA[biological nitrogen fixation]]></category>
		<category><![CDATA[biological nitrogen fixation in crop production]]></category>
		<category><![CDATA[biomass allocation]]></category>
		<category><![CDATA[Bradyrhizobium japonicum]]></category>
		<category><![CDATA[cowpea]]></category>
		<category><![CDATA[Cowpea nitrogen fixation]]></category>
		<category><![CDATA[cowpea nodulation trials]]></category>
		<category><![CDATA[crop-soil-microbe interactions in legume cultivation]]></category>
		<category><![CDATA[effects of native vs. introduced rhizobia]]></category>
		<category><![CDATA[impact of heat treatment on soil microbes]]></category>
		<category><![CDATA[legume crop resilience in sub-Saharan Africa]]></category>
		<category><![CDATA[microbial partnership in smallholder farming]]></category>
		<category><![CDATA[nodulation]]></category>
		<category><![CDATA[rhizobia inoculant performance]]></category>
		<category><![CDATA[rhizobial inoculation]]></category>
		<category><![CDATA[role of Sinorhizobium fredii in legume growth]]></category>
		<category><![CDATA[sandy loam soil]]></category>
		<category><![CDATA[Sinorhizobium fredii]]></category>
		<category><![CDATA[soil microbial communities in agriculture]]></category>
		<category><![CDATA[soil microbiology]]></category>
		<category><![CDATA[sustainable agriculture]]></category>
		<category><![CDATA[sustainable soil fertility practices]]></category>
		<category><![CDATA[symbiotic effectiveness]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=231918</guid>

					<description><![CDATA[A controlled screenhouse trial shows Sinorhizobium fredii inoculation produces the highest nodulation, biomass and symbiotic advantage in cowpea under both heat-treated and unsterilised sandy loam soils.]]></description>
										<content:encoded><![CDATA[<p>For millions of smallholder farmers across sub-Saharan Africa, cowpea is more than a crop. It is a staple source of dietary protein, a soil builder that feeds nitrogen back into exhausted fields, and a buffer against hunger in regions where synthetic fertiliser is scarce or unaffordable. The engine behind that resilience is a microscopic partnership: soil bacteria known as rhizobia infect the plant&#8217;s roots and form nodules, specialised organs in which atmospheric nitrogen is converted into forms the plant can use. A new screenhouse study from Nigerian and Ghanaian researchers, published in Discover Soil, has now put that partnership under an unusually rigorous microscope, tracking how two commercial inoculant strains perform when the surrounding soil microbial community is either left intact or deliberately suppressed by heat.</p>
<p>The research team, led by James Ukwumonu Yahaya of the University of Ilorin and the University of Ghana, grew cowpea variety Sampea15 in pots filled with sandy loam soil collected from a long-cultivated agricultural field. The soil was split into two contrasting treatments. One portion was left unsterilised, preserving its native microbial community, including indigenous rhizobia that had built up over years of legume and cereal cropping. The other was dry-heated at 160 degrees Celsius for two hours to drastically reduce the microbial load. Into these two soil environments the researchers introduced four nitrogen regimes: inoculation with Sinorhizobium fredii strain N8, inoculation with the reference strain Bradyrhizobium japonicum USDA 110, mineral nitrogen supplied as urea at 90 kilograms of nitrogen per hectare, and a non-inoculated control. The eight treatment combinations were arranged in a completely randomised design with three replicates and monitored for ten weeks after planting.</p>
<p>The choice of strains was deliberate. S. fredii was selected for its broad host range, rapid growth, and documented effectiveness in legume symbiosis, while B. japonicum USDA 110 served as a widely used benchmark in rhizobial research. Seeds were surface sterilised with ethanol and sodium hypochlorite before planting to ensure that any nodulation observed could be attributed to soil-borne or applied bacteria rather than seed-borne contaminants. Inoculum was standardised to roughly 10 to the power of 8 colony-forming units per millilitre, a concentration regarded as effective for legume studies, and applied at one millilitre per seed immediately before sowing.</p>
<p>The nodulation results were striking. Under unsterilised soil, nodules appeared as early as two weeks after planting, and S. fredii-inoculated plants quickly pulled ahead, climbing from 3.00 nodules per plant at two weeks to a peak of 74.00 nodules per plant at ten weeks, the highest figure recorded anywhere in the experiment. B. japonicum followed a similar but lower trajectory, reaching 46.00 nodules per plant at ten weeks. The non-inoculated control in unsterilised soil produced only 10.00 nodules per plant by the end of the trial, a baseline that reflects the activity of native rhizobia naturally present in the field soil. Under heat-treated soil, the picture changed dramatically: most treatments produced no nodules at all during the first four weeks, and nodulation did not begin in earnest until around week six. Even so, S. fredii again dominated, finishing with 45.33 nodules per plant compared with 27.00 for B. japonicum and just 5.00 for the non-inoculated control.</p>
<p>That residual nodulation in the heat-treated control is itself scientifically revealing. Rhizobia are non-spore-forming organisms, so true thermal persistence is considered unlikely. The authors suggest the late-appearing nodules in the treated control probably arose from external contamination during irrigation or handling, or from microbes sheltered within soil aggregates that shielded them from the oven&#8217;s heat. The finding underscores a persistent methodological headache in inoculant research: complete sterilisation of soil is notoriously difficult to achieve, and even aggressive heat treatment can leave enough biological activity to muddy the interpretation of results. It also means the study&#8217;s contrasts should be read as effects of heat-treated soil conditions rather than as direct proof that microbial abundance was reduced to zero, a caveat the authors state explicitly.</p>
<p>Growth and biomass data reinforced the nodulation story. Plants receiving mineral nitrogen grew taller early on, an expected consequence of immediately available nitrogen, but that advantage faded as the season progressed. Inoculated treatments, particularly those given S. fredii, maintained steady vegetative growth throughout, and by harvest the inoculated plants had produced the highest shoot and root biomass. S. fredii treatments recorded shoot biomass of 5.70 grams per plant and root biomass between 2.70 and 2.80 grams per plant, the largest values in the study. Leaf number and stem girth followed similar patterns, with the clearest separation between treatments appearing under heat-treated soil, where the absence of a buffering native community allowed inoculant performance to shine through. In unsterilised soil, resident microbes lifted the baseline for every treatment, compressing the apparent differences between inoculated and uninoculated plants.</p>
<p>The study&#8217;s most methodologically interesting contribution lies in its integrative indices, which go beyond the single-parameter assessments that dominate much of the inoculant literature. The researchers calculated a nodulation biomass efficiency ratio, expressing shoot biomass produced per nodule; a biomass allocation ratio, the quotient of root to shoot biomass; and a symbiotic advantage index, which measures the biomass gain of inoculated plants relative to uninoculated controls. These indices separated the treatments far more sharply than nodule counts or biomass alone. S. fredii treatments posted symbiotic advantage index values of 1.08 under unsterilised soil and 1.01 under heat-treated soil, meaning inoculated plants more than doubled the biomass of their uninoculated counterparts. B. japonicum trailed with values of 0.91 and 0.85 respectively. The biomass allocation ratio was also highest in S. fredii treatments, at 0.49 and 0.47, signalling greater investment in the root systems where nodules form and nitrogen fixation takes place.</p>
<p>Pearson correlation analysis at ten weeks added statistical muscle to these interpretations. Nodulation correlated positively with root biomass (r = 0.819), biomass allocation ratio (r = 0.840), the symbiotic advantage index (r = 0.552), and shoot biomass (r = 0.437). Root biomass itself showed an almost perfect association with the allocation ratio (r = 0.980) and a strong link to the symbiotic advantage index (r = 0.797). The nodulation biomass efficiency ratio, by contrast, correlated negatively with nodulation, root biomass, and allocation, an artefact of its mathematical structure rather than a sign of biological inferiority, since heavily nodulated plants inevitably produce less biomass per individual nodule. Treatment-level correlations revealed near-identical response patterns between the two inoculants within each soil type, with coefficients approaching 1.000, while non-inoculated controls clustered apart, confirming that inoculation, not soil condition alone, drove the performance differences.</p>
<p>The mineral nitrogen results carry practical weight for fertiliser policy. Urea supported early shoot growth but did not translate into greater root biomass or symbiotic efficiency, and nodulation, while not completely suppressed at the applied rate, remained well below that of inoculated treatments. The authors interpret this as a shift in carbon allocation away from roots and nodulation structures when external nitrogen is readily available, a well-documented antagonism between mineral nitrogen supply and biological nitrogen fixation. In other words, fertiliser buys a fast start, but an effective rhizobial partnership delivers sustained nitrogen nutrition together with the root development that supports water and nutrient uptake, all without the cost and emissions associated with synthetic nitrogen.</p>
<p>The researchers are careful about the limits of their work. Indigenous rhizobial populations were not quantified before planting using the most probable number technique, no molecular characterisation confirmed the identity of the S. fredii isolate, and nodule occupancy and nitrogenase activity were not measured, so the indices capture symbiotic performance indirectly rather than fixing nitrogen directly. They recommend molecular confirmation, field validation over multiple seasons, direct enumeration of native rhizobia before and after soil treatment, and routine adoption of integrative indices in inoculant screening. Even with those caveats, the message is clear: Sinorhizobium fredii strain N8 outperformed the reference strain across both microbial environments and emerges as a strong biofertiliser candidate for cowpea in comparable agroecological zones, while the study&#8217;s combined nodulation-biomass framework offers a sharper lens for judging which inoculants actually deliver in the messy, microbially crowded soils that farmers actually plant.</p>
<p><strong>Subject of Research:</strong> Rhizobial inoculation effects on nodulation and biomass allocation in cowpea under contrasting soil microbial conditions</p>
<p><strong>Article Title:</strong> Integrative evaluation of symbiotic performance and biomass allocation in rhizobial inoculated cowpea under contrasting soil microbial conditions</p>
<p><strong>Article References:</strong> Yahaya, J. U., Fawole, O. B., Lawal, O. I., Dada, H. A., &amp; Ikuoponiyi, D. A. (2026). Integrative evaluation of symbiotic performance and biomass allocation in rhizobial inoculated cowpea under contrasting soil microbial conditions. <em>Discover Soil, 3</em>(1), Article 125. <a href="https://doi.org/10.1007/s44378-026-00269-y" rel="noopener noreferrer">https://doi.org/10.1007/s44378-026-00269-y</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44378-026-00269-y" rel="noopener noreferrer">10.1007/s44378-026-00269-y</a></p>
<p><strong>Keywords:</strong> cowpea, rhizobial inoculation, Sinorhizobium fredii, Bradyrhizobium japonicum, biological nitrogen fixation, nodulation, biomass allocation, symbiotic effectiveness, soil microbiology, sandy loam soil, biofertilizer, sustainable agriculture</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">231918</post-id>	</item>
		<item>
		<title>A Single Genetic Enhancer Helped Turn Wild Teosinte into High-Yielding Maize</title>
		<link>https://scienmag.com/a-single-genetic-enhancer-helped-turn-wild-teosinte-into-high-yielding-maize/</link>
		
		<dc:creator><![CDATA[Alan Morgan]]></dc:creator>
		<pubDate>Sun, 13 Sep 2026 00:55:37 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[biomass allocation]]></category>
		<category><![CDATA[domestication genes in maize]]></category>
		<category><![CDATA[enhancer]]></category>
		<category><![CDATA[evolutionary history of maize]]></category>
		<category><![CDATA[genetic basis of crop productivity]]></category>
		<category><![CDATA[genetic enhancer role in crop yield]]></category>
		<category><![CDATA[genetic factors influencing harvest efficiency]]></category>
		<category><![CDATA[grain yield]]></category>
		<category><![CDATA[harvest index]]></category>
		<category><![CDATA[harvest index in cereal crops]]></category>
		<category><![CDATA[HI1]]></category>
		<category><![CDATA[impact of selection on plant architecture]]></category>
		<category><![CDATA[maize domestication]]></category>
		<category><![CDATA[Maize domestication genetics]]></category>
		<category><![CDATA[maize genetic modification for high yield]]></category>
		<category><![CDATA[Nature Plants]]></category>
		<category><![CDATA[near-isogenic lines]]></category>
		<category><![CDATA[plant breeding]]></category>
		<category><![CDATA[plant resource allocation during domestication]]></category>
		<category><![CDATA[pleiotropy]]></category>
		<category><![CDATA[QTL mapping]]></category>
		<category><![CDATA[teosinte]]></category>
		<category><![CDATA[teosinte to maize evolutionary transformation]]></category>
		<category><![CDATA[wild grass transformation into staple crop]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=200264</guid>

					<description><![CDATA[Researchers identified a domestication-selected enhancer, Harvest Index 1, that helped raise maize harvest index by 81 percent compared with its wild ancestor teosinte.]]></description>
										<content:encoded><![CDATA[<p>One of the most dramatic transformations in the history of agriculture took place roughly nine thousand years ago in the valleys of southern Mexico, when Indigenous farmers began propagating teosinte, a wild grass with a sprawling, branching habit and a handful of hard-cased kernels, into the plant we now know as maize. Over millennia of selection, that grass was reshaped into one of the world&#8217;s most productive cereal crops. A new study published in Nature Plants, highlighted by editor Jun Lyu, adds an important piece to the genetic story of this transformation by showing that the domestication of maize substantially influenced a trait of enormous practical consequence: harvest index, the fraction of a plant&#8217;s total biomass that ends up in the harvested grain.</p>
<p>Harvest index sits at the heart of crop productivity. It is the ratio of grain yield to total above-ground biomass, and it captures how efficiently a plant partitions its resources between the parts people eat and the parts they do not. While decades of research have documented how maize domestication restructured the plant&#8217;s overall architecture and the architecture of its male and female inflorescences, the question of whether and how domestication genetically shaped harvest index had remained open. Answering that question requires comparing wild, traditional, and modern material in a controlled framework, and that is precisely what a research team led by Li Guo of China Agricultural University set out to do.</p>
<p>The team assembled a diversity panel that spans the full arc of maize evolution: thirty lines of teosinte, the wild ancestor; twenty maize landraces, representing the semi-domesticated forms grown by early farmers; and fifty modern inbred lines, the elite genetic material that underpins contemporary maize breeding. By evaluating harvest index across these three groups, the researchers quantified the cumulative effect of domestication on this trait. The result was striking. On average, domestication increased harvest index by 81 percent, meaning that modern maize devotes a dramatically larger share of its total plant mass to grain than its wild progenitor does.</p>
<p>An 81 percent increase is not a subtle adjustment. It reflects a deep reorganization of how the maize plant allocates carbon, nutrients, and developmental resources. Wild teosinte invests heavily in stems, branches, tassels, and protective structures that help it survive in the wild, but produce little food. Domesticated maize, through the combined action of many genes selected over generations, was redirected toward producing large, exposed ears packed with kernels. Understanding which genetic elements underlie this shift is essential both for reconstructing the history of the crop and for guiding future breeding efforts, particularly as breeders seek to push yield gains further in the face of climate change and growing global demand for grain.</p>
<p>To dissect the genetics behind the shift, Guo and colleagues turned to quantitative trait locus mapping, a classical but powerful technique that links regions of the genome to measurable trait differences in segregating populations. The researchers created two maize-teosinte crossing populations, each mixing chromosomes from the wild ancestor and domesticated maize in different combinations, and then mapped which genomic intervals were associated with variation in harvest index. The scan identified twenty quantitative trait loci, confirming that harvest index is a genetically complex trait shaped by many loci spread across the maize genome, as expected for a trait so tightly connected to overall plant growth and partitioning.</p>
<p>Among those twenty loci, one stood out. A major locus, which the researchers named Harvest Index 1, or HI1, showed consistent and large effects in both crossing populations. Consistency across independent populations is an important signal in genetics: it indicates that the effect is real and robust rather than an artifact of a particular cross. The magnitude of the HI1 effect, together with its reproducibility, marks it as a principal genetic contributor to the harvest index difference between teosinte and maize.</p>
<p>To pin down the function of HI1 more precisely, the team used near-isogenic lines, pairs of plants that are genetically almost identical except for a small chromosome segment carrying either the teosinte or the maize version of the locus. This design isolates the effect of the target gene from the noise of the rest of the genome. When the researchers compared near-isogenic lines carrying the maize allele of HI1 with those carrying the teosinte allele, they confirmed that the maize allele increases harvest index. But the locus also influenced total biomass and grain weight, revealing a pleiotropic effect: a single genetic change simultaneously affecting multiple traits of the plant.</p>
<p>Pleiotropy is a recurring theme in crop domestication genetics. The best-known domestication genes in maize, such as those controlling branching and glume architecture, also produce coordinated suites of changes, because the regulatory variants involved often act on shared developmental pathways rather than on a single trait. The apparent role of HI1 in modulating biomass and grain weight alongside harvest index suggests it may tune the growth and partitioning machinery of the plant more broadly, rather than acting narrowly on grain fill alone. Notably, as the research highlight&#8217;s framing emphasizes, HI1 joins a growing list of domestication-selected enhancers, regulatory DNA elements that altered gene expression under human selection rather than changes in the protein-coding sequence itself. This regulatory mode of domestication has emerged as a hallmark of how early farmers, deliberately or not, reshaped crops: subtle changes in when and where genes are turned on can reorganize a plant&#8217;s architecture without breaking the genes outright.</p>
<p>The identification of HI1 carries implications well beyond evolutionary history. Harvest index has been a cornerstone of modern yield improvement, and the gains achieved during the Green Revolution of the twentieth century came largely from breeding varieties that invested more heavily in grain and less in straw. Knowing the specific loci that raise harvest index gives breeders molecular targets for the next round of improvement, and the teosinte alleles preserved at loci like HI1 represent a reservoir of functional variation that could be deployed either to boost or, in some contexts, to rebalance trait architecture. As genomic tools make it increasingly feasible to edit or introgress specific regulatory regions, the boundary between the wild ancestor and the modern crop becomes not just a historical record but a practical resource. The study of harvest index during maize domestication, with HI1 as its newly identified centerpiece, illustrates how a single enhancer selected by ancient farmers continues to shape the productivity of one of humanity&#8217;s most important food crops, and how decoding the genetic logic of domestication can inform the future of crop improvement.</p>
<p><strong>Subject of Research:</strong> Identification of a domestication-selected enhancer, Harvest Index 1, that increased harvest index during maize domestication</p>
<p><strong>Article Title:</strong> Yet another domestication-selected enhancer</p>
<p><strong>Article References:</strong> Lyu, J. (2026). Yet another domestication-selected enhancer. <em>Nature Plants</em>. <a href="https://doi.org/10.1038/s41477-026-02416-3" rel="noopener noreferrer">https://doi.org/10.1038/s41477-026-02416-3</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1038/s41477-026-02416-3" rel="noopener noreferrer">10.1038/s41477-026-02416-3</a></p>
<p><strong>Keywords:</strong> maize domestication, teosinte, harvest index, HI1, enhancer, QTL mapping, near-isogenic lines, plant breeding, biomass allocation, grain yield, pleiotropy, Nature Plants</p>
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