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	<title>perennial grasses &#8211; Science</title>
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	<title>perennial grasses &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>The Kengyilia hirsuta karyotype polymorphisms as revealed by FISH with tandem repeats and single-gene probes</title>
		<link>https://scienmag.com/the-kengyilia-hirsuta-karyotype-polymorphisms-as-revealed-by-fish-with-tandem-repeats-and-single-gene-probes/</link>
		
		<dc:creator><![CDATA[Juliet Wilcox]]></dc:creator>
		<pubDate>Tue, 20 Oct 2026 11:01:17 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[Science News]]></category>
		<category><![CDATA[chromosomal diversity in cold- and drought-tolerant grasses]]></category>
		<category><![CDATA[chromosomal translocations]]></category>
		<category><![CDATA[chromosome mapping]]></category>
		<category><![CDATA[chromosome variation in Qinghai populations]]></category>
		<category><![CDATA[conservation of gene order in wheat relatives]]></category>
		<category><![CDATA[FISH analysis of grass genomes]]></category>
		<category><![CDATA[fluorescence in situ hybridization]]></category>
		<category><![CDATA[fluorescence in situ hybridization in grass species]]></category>
		<category><![CDATA[genome organization]]></category>
		<category><![CDATA[genomic organization of Kengyilia species]]></category>
		<category><![CDATA[hirsuta]]></category>
		<category><![CDATA[karyotype polymorphism]]></category>
		<category><![CDATA[karyotype polymorphisms in perennial grasses]]></category>
		<category><![CDATA[Kengyilia]]></category>
		<category><![CDATA[Kengyilia hirsuta]]></category>
		<category><![CDATA[Kengyilia hirsuta chromosome map]]></category>
		<category><![CDATA[perennial grasses]]></category>
		<category><![CDATA[Qinghai populations]]></category>
		<category><![CDATA[structural chromosome rearrangements in Triticeae]]></category>
		<category><![CDATA[structural rearrangements in Y]]></category>
		<category><![CDATA[tandem repeat and single-gene probes in plant cytogenetics]]></category>
		<category><![CDATA[Triticeae]]></category>
		<category><![CDATA[wheat relatives]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=318089</guid>

					<description><![CDATA[A cytogenetic study of 29 Kengyilia hirsuta plants from seven Qinghai populations identified 47 chromosome variants and mapped conserved and rearranged regions relative to wheat chromosomes.]]></description>
										<content:encoded><![CDATA[<p>Researchers have constructed a chromosome-level map of the perennial grass <em>Kengyilia hirsuta</em>, revealing strong conservation of gene order in its St genome, several structural rearrangements in the Y and P genomes, and 47 chromosome variants among 29 plants from seven populations in Qinghai, China. The study used fluorescence in situ hybridization (FISH), genomic in situ hybridization and repetitive-sequence probes to identify the chromosomes, establish their correspondence with the seven homoeologous groups of common wheat and characterize variation within natural populations. The reference karyotype was based on plants from the Haiyan population, while the broader survey covered seven locations. These findings provide a physical framework for locating genes in a cold- and drought-tolerant perennial relative of wheat, although the study did not isolate or validate any trait gene.</p>
<p><em>Kengyilia hirsuta</em> is a member of the grass tribe Triticeae and a close wild relative of wheat. The source material describes approximately 32 documented species and subspecies in the genus, which occurs in meadows, steppes, forest fringes and dry or semi-desert habitats across central Asia and the Qinghai–Tibetan Plateau. <em>K. hirsuta</em> is distributed in Qinghai and Gansu and grows in sandy areas at high elevations. It is characterized by tall stalks, high seed-setting rates and mild seed shattering, making it a potential candidate for perennial grain development. Its chromosome complement consists of St, Y and P genomes, conventionally denoted StPY; the St genome is associated with <em>Pseudoroegneria</em>, the P genome with <em>Agropyron</em>, and the origin of the Y genome remains unknown. The species’ large, repetitive and complex genome makes targeted gene discovery difficult, even with modern sequencing methods.</p>
<p>For the reference analysis, the investigators selected 14 full-length complementary DNA probes that had previously been mapped to the short and long arms of the seven homoeologous chromosome groups in common wheat. Most probes produced the expected six FISH signals in <em>K. hirsuta</em>, corresponding to a site on each member of its three paired chromosome sets. Probe 6L-1 produced eight signals, while 7S-1 produced 10, indicating that some gene-associated sequences were present on more than one chromosome. The researchers then used sequential hybridizations with probes for 45S ribosomal DNA, 5S ribosomal DNA, pAs1 and the (AAG)<sub>10</sub> tandem repeat to identify additional landmarks. A final round of genomic in situ hybridization with DNA from <em>Pseudoroegneria stipifolia</em> and <em>Agropyron cristatum</em> assigned the identified chromosomes to the St, Y and P genomes. The sequential procedure produced a molecular karyotype and idiogram in which each chromosome was associated with both gene-probe and repeat-probe positions.</p>
<p>Chromosome measurements showed that the three genomes differed markedly in size. St chromosomes ranged from 6.60 to 8.76 micrometres in length and averaged 7.68 micrometres, while Y chromosomes ranged from 5.54 to 7.56 micrometres and averaged 6.55 micrometres. P chromosomes were substantially larger, measuring 11.70 to 14.21 micrometres with an average of 12.96 micrometres. Long-arm to short-arm ratios ranged from 1.07 to 2.13 in the St genome, 1.09 to 2.08 in the Y genome and 1.12 to 1.90 in the P genome. Repeated sequences also supplied recognizable landmarks: 1St and 5St carried 5S and 45S ribosomal DNA sites on their short arms, respectively; 1P had a major 45S site in the telomeric region of its short arm; 5P carried separated 5S and 45S sites; and 7P displayed dispersed pAs1 signals on both arms. These markers allow chromosomes to be recognized even where repeat patterns differ among individuals.</p>
<p>Comparison with common wheat showed that the St genome was the most strongly conserved. All 14 single-gene probes hybridized at their expected positions in the corresponding St chromosomes, indicating a high degree of chromosomal synteny. The Y genome retained much of the same organization but contained localized departures. The 7S-1 probe produced an additional interstitial signal on 3Y, and both 7S-1 and 7L-4 mapped to the long arm of 7Y, a pattern consistent with a pericentric inversion. The researchers also noted a 5S ribosomal DNA site on 2Y even though 1Y lacked one, suggesting that a rearrangement may have transferred the site between these chromosomes. These interpretations are based on probe positions and were presented as structural assignments rather than as complete sequence-level descriptions of the affected regions.</p>
<p>The P genome displayed the greatest distortion of wheat-like collinearity. The 2S-1 and 4S-6 probes hybridized on 4P, whereas 2L-1 and 4L-4 signals appeared on 2P, leading the team to interpret chromosomes 2P and 4P as reciprocal translocation chromosomes. They tentatively designated these as 4PL/2PL and 2PS/4PS, pending further structural evidence. Additional hybridization of 6L-1 was detected in the subtelomeric long-arm region of 1P, and an additional 7S-1 site occurred in the telomeric short-arm region of 2P. Comparisons with <em>A. cristatum</em> indicated that the 2P–4P reciprocal translocation may be an ancient feature shared by the two species, while other structural differences distinguished their 1P chromosomes. <em>K. hirsuta</em> also lacked the paracentric inversion on the long arm of 6P previously reported in <em>A. cristatum</em>.</p>
<p>The population survey used the repeat probes as chromosomal landmarks to karyotype 29 individuals from seven locations: Guinan, Haiyan, Gangcha and Qilian in Qinghai. It identified 47 variants in total, comprising 19 in the St genome, 16 in the Y genome and 12 in the P genome. Most variants were changes in the presence, absence, duplication or deletion of pAs1, (AAG)<sub>10</sub> or ribosomal DNA hybridization sites rather than differences affecting entire chromosome sets. Chromosomes 1St, 5Y, 6Y, 4P, 6P and 7P had identical variants across the populations and were the most stable, whereas 7St was the most variable, with more than three forms. A tentative pericentric inversion was identified in 5P in different populations. The sampled populations did not contain equal numbers of individuals, so the survey describes the chromosomes represented by this collection rather than providing a complete estimate of diversity throughout the species’ range.</p>
<p>Less common rearrangements occurred in individual plants. A chromosome carrying a P-genome segment within a Y chromosome was identified in the GCN population, consistent with an inter-genomic translocation. In the HCZ population, a reciprocal translocation involving 4Y and 3P was detected. The Qilian sample showed the greatest chromosome heterozygosis: all five sampled individuals had mixed chromosome states, equivalent to 80 percent heterozygosis in that population. Across the complete sample, 10 of 29 plants, or 34.48 percent, had heterozygous karyotypes. The researchers suggested that this pattern may indicate outcrossing, but they did not directly measure reproductive behavior. The proposed origin of <em>Kengyilia</em> through natural hybridization between an StY species and the P-genome species <em>A. cristatum</em> provides a possible context for such variation, while the role of facultative allogamy remains unresolved.</p>
<p>The chromosome map could assist targeted gene discovery in group 3, whose relevance to domestication was illustrated by the conserved locations of the seed-shattering genes <em>Btr-1</em> and <em>Btr-2</em> on the short arms of group 3 chromosomes in barley and wheat. The study found conserved synteny in 3St and 3P and possible structural change in 3Y. It also established that group 3 chromosomes could be recognized with specific markers, providing a basis for their possible isolation by flow sorting or microdissection. More generally, knowledge of collinearity and rearrangement helps determine whether a chromosome segment can be compared directly with the annotated wheat genome or whether structural differences must first be accounted for. The study did not transfer genes or produce a perennial crop, so its contribution is a cytogenetic reference rather than proof of improved breeding performance.</p>
<p>The ribosomal DNA findings also supplied useful but unresolved targets for further research. In <em>K. hirsuta</em>, 45S rDNA sites were mapped to the short arms of 5St, 1P and 5P, and the positions in 1P and 5P were consistent with those in the P genome of <em>A. cristatum</em>. The placement of 45S, 5S or both on the short arms of group 5 chromosomes across the three genomes was also consistent with the strong conservation of that group in common wheat. Population differences in whether 45S or 5S signals were present could reflect copy-number or positional variation, and 2P sometimes carried an additional 5S site. The authors noted that rDNA copy number and location may be sensitive to genomic stress and may contribute to adaptive responses, but they did not establish that the observed variants were caused by stress or associated with population differentiation. The resulting karyotype offers a detailed physical framework for testing those questions and for investigating the genetic basis of useful traits in <em>K. hirsuta</em>.</p>
<p><strong>Subject of Research:</strong> Chromosomal organization and karyotype variation in the perennial wheat relative Kengyilia hirsuta</p>
<p><strong>Article Title:</strong> The Kengyilia hirsuta karyotype polymorphisms as revealed by FISH with tandem repeats and single-gene probes</p>
<p><strong>Article References:</strong> Tao, X., Liu, B., &amp; Dou, Q. (2021). The Kengyilia hirsuta karyotype polymorphisms as revealed by FISH with tandem repeats and single-gene probes. <em>Comparative Cytogenetics, 15</em>(4), 375-392. <a href="https://doi.org/10.3897/compcytogen.v15.i4.71525" rel="noopener noreferrer">https://doi.org/10.3897/compcytogen.v15.i4.71525</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3897/compcytogen.v15.i4.71525" rel="noopener noreferrer">10.3897/compcytogen.v15.i4.71525</a></p>
<p><strong>Keywords:</strong> Kengyilia hirsuta, fluorescence in situ hybridization, chromosome mapping, karyotype polymorphism, Triticeae, wheat relatives, genome organization, chromosomal translocations, perennial grasses, Qinghai populations, Kengyilia, hirsuta</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">318089</post-id>	</item>
		<item>
		<title>Nine-Year Field Trial Reveals Which Perennial Grasses Best Restore Degraded Semi-Arid Soils</title>
		<link>https://scienmag.com/nine-year-field-trial-reveals-which-perennial-grasses-best-restore-degraded-semi-arid-soils/</link>
		
		<dc:creator><![CDATA[Alan Morgan]]></dc:creator>
		<pubDate>Wed, 07 Oct 2026 11:48:16 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[Bundelkhand]]></category>
		<category><![CDATA[carbon management index]]></category>
		<category><![CDATA[climate resilience in semi-arid agriculture]]></category>
		<category><![CDATA[comparison of grass species for degraded land]]></category>
		<category><![CDATA[Degraded semi-arid soil restoration]]></category>
		<category><![CDATA[drought-prone region land rehabilitation]]></category>
		<category><![CDATA[fodder productivity]]></category>
		<category><![CDATA[grass species effectiveness in soil fertility restoration]]></category>
		<category><![CDATA[guinea grass]]></category>
		<category><![CDATA[impact of irrigation on grass-based soil restoration]]></category>
		<category><![CDATA[Indian grassland research for soil restoration]]></category>
		<category><![CDATA[irrigation]]></category>
		<category><![CDATA[Land degradation]]></category>
		<category><![CDATA[long-term field trial soil recovery]]></category>
		<category><![CDATA[perennial grasses]]></category>
		<category><![CDATA[perennial grasses for soil improvement]]></category>
		<category><![CDATA[restoration efficiency index]]></category>
		<category><![CDATA[semi-arid agroecosystems]]></category>
		<category><![CDATA[semi-arid land degradation solutions]]></category>
		<category><![CDATA[soil microbial biomass]]></category>
		<category><![CDATA[soil organic carbon]]></category>
		<category><![CDATA[soil organic carbon enhancement in semi-arid regions]]></category>
		<category><![CDATA[soil restoration]]></category>
		<category><![CDATA[sustainable land management in semi-arid ecosystems]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=244329</guid>

					<description><![CDATA[A nine-year Indian field trial found that guinea grass and a tri-specific hybrid grass most effectively rebuilt soil carbon, fertility, and microbial health in degraded semi-arid land, with irrigation amplifying gains and the hybrid showing superior drought resilience.]]></description>
										<content:encoded><![CDATA[<p>In the drought-prone Bundelkhand region of central India, where summer temperatures can climb to 49 degrees Celsius and nearly all of the year&#8217;s roughly 908 millimeters of rain falls in just four monsoon months, a nine-year field experiment has delivered some of the clearest evidence yet that the right perennial grass can rebuild a broken landscape. Researchers at the ICAR-Indian Grassland and Fodder Research Institute in Jhansi set out to answer a deceptively simple question: if you plant degraded semi-arid farmland with perennial grasses, which species actually restores the soil best, and does it matter whether you irrigate? Their answer, published in the open-access journal Discover Soil, carries practical weight for the roughly one-quarter of Earth&#8217;s land surface now classified as degraded.</p>
<p>The team, led by Mukesh Choudhary and Mahendra Prasad, compared four perennial grasses over nine consecutive growing seasons from 2015-16 to 2023-24: guinea grass (Megathyrsus maximus), a tri-specific hybrid (TSH), the bajra-napier hybrid (BNH), and the hardy rangeland grass Cenchrus ciliaris. Each species was grown under two contrasting moisture regimes, rainfed and irrigated, in a factorial randomized block design with three replications. The starting point was a sandy clay loam classified as a Typic Haplustept, with soil organic carbon of just 5.0 grams per kilogram in the top 15 centimeters, available nitrogen of 170 kilograms per hectare, and the low fertility typical of a region battered by recurrent drought, shallow undulating soils, and potential evapotranspiration of 2,565 millimeters per year.</p>
<p>The headline finding is that guinea grass emerged as the standout restoration champion. Under irrigation it produced a mean green fodder yield of 85.9 tonnes per hectare and dry fodder yield of 20.4 tonnes per hectare, increases of 37.0 and 28.3 percent over rainfed conditions. More importantly for soil health, irrigated guinea grass plots recorded the highest total organic carbon of any treatment, 9.56 grams per kilogram in the surface soil, along with the greatest hot water soluble carbon (146.13 milligrams per kilogram), particulate organic carbon (6.12 grams per kilogram), labile carbon (371.75 milligrams per kilogram), and soil microbial biomass carbon (365.83 micrograms per gram). These values exceeded the tri-specific hybrid, bajra-napier hybrid, and Cenchrus ciliaris by margins ranging from 2 percent to as much as 234 percent depending on the indicator.</p>
<p>Across all species, irrigation proved a powerful amplifier of both productivity and soil recovery. Green fodder yields rose by 11.9 to 44.7 percent under irrigation compared with rainfed conditions, and dry yields by 5.5 to 34.4 percent. Below ground, irrigation lifted total organic carbon by about 5 percent, hot water soluble carbon by roughly 19 percent, particulate organic carbon by about 12 percent, labile carbon by around 6 percent, and microbial biomass carbon by approximately 23 percent. Carbon buildup relative to the experiment&#8217;s starting conditions ranged from 3 to 41 percent under rainfed management and climbed to 5 to 49 percent with irrigation, with guinea grass and the tri-specific hybrid consistently at the top of that range. Available nitrogen, phosphorus, and potassium followed the same pattern, with guinea grass under irrigation increasing nutrient availability by 5.8 to 16.6 percent relative to its rainfed counterpart.</p>
<p>To move beyond single measurements, the researchers deployed two composite metrics. The carbon management index, which combines a carbon pool index with a lability index against a reference fallow soil, exceeded 185 under guinea grass in both moisture regimes, a value well above the threshold of 100 that signals sustainable soil management. Under irrigation, guinea grass posted a carbon management index 21, 45, and 75 percent higher than the tri-specific hybrid, bajra-napier hybrid, and Cenchrus ciliaris respectively. The team also introduced a restoration efficiency index, a weighted composite integrating productivity, soil fertility, microbial health, and soil carbon dynamics, with biological recovery and carbon restoration weighted at 0.30 each. Guinea grass scored above 80 percent, the study&#8217;s threshold for high restoration efficiency, in both rainfed (86.7 percent) and irrigated (84.8 percent) conditions, while Cenchrus ciliaris languished at the bottom.</p>
<p>Interestingly, the tri-specific hybrid revealed a different kind of strength. Although its absolute yields and carbon metrics trailed guinea grass, it suffered the smallest penalty when the irrigation was switched off: its irrigated green fodder yield of 78.6 tonnes per hectare was only 12.0 percent above its rainfed yield, and its dry yield just 5.5 percent higher. That drought resilience translated into moderate restoration efficiency under rainfed conditions, with a carbon management index of at least 150 and a restoration efficiency index above 60 percent. The authors&#8217; practical recommendation therefore splits by context: guinea grass for maximizing biomass and soil carbon restoration wherever water allows, and the tri-specific hybrid as the more reliable choice for purely rainfed systems.</p>
<p>The study also probed the quality and vertical distribution of the carbon being accumulated. The recalcitrant index, the proportion of carbon resistant to acid hydrolysis, varied only narrowly, from 95.91 to 97.13 percent, with Cenchrus ciliaris and the bajra-napier hybrid tending toward slightly higher values. The authors interpret the lower recalcitrant index under guinea grass and the tri-specific hybrid not as a weakness but as evidence of active carbon cycling, with abundant labile fractions turning over rapidly in these biologically vigorous rhizospheres. In soils this depleted, they argue, carbon sink strength is limited primarily by the quantity of carbon inputs rather than by the soil&#8217;s capacity to stabilize them. Stratification ratios, comparing surface to subsurface carbon pools, ranged from 0.89 to 1.22 and trended higher under irrigation, consistent with litter, fine root turnover, and rhizodeposition enriching the upper 15 centimeters of the profile.</p>
<p>Correlation and network analyses added a systems-level view of how restoration proceeds. Soil organic carbon correlated almost perfectly with total organic carbon (r = 1.00) and very strongly with microbial biomass carbon (r = 0.97), particulate organic carbon (r = 0.95), labile carbon (r = 0.95), and the carbon management index (r = 0.95). Microbial biomass carbon itself tracked available nitrogen at r = 0.99. Within the correlation network, built from significant correlations of r at or above 0.85, the variables with the greatest connector importance were the carbon management index, labile carbon, microbial quotient, particulate organic carbon, and microbial biomass carbon, marking them as the most informative sentinels of recovery. The restoration efficiency index behaved differently, correlating negatively with these indicators, which the authors attribute to the mathematical structure of the composite index rather than any biological trade-off, and they candidly flag indicator redundancy and the author-defined weighting scheme as limitations requiring validation in independent datasets.</p>
<p>The broader significance is considerable. Land degradation undermines food security, biodiversity, and climate resilience worldwide, and restoring degraded lands is embedded in the United Nations Sustainable Development Goals. Perennial grasses work as restoration agents because their deep, persistent root networks pump carbon below ground year after year, stabilize aggregates, reduce erosion, and feed the microbial communities that drive nutrient cycling. This trial shows that species choice and water availability jointly determine how fast that recovery happens, and it offers farmers and land managers in semi-arid regions a concrete, evidence-based menu: guinea grass where biomass and carbon gains are the priority, the tri-specific hybrid where drought risk dominates. The authors caution that the study covered a limited set of species in a single semi-arid environment, that the persistence of these gains under future climate variability remains untested, and that microbial community dynamics, greenhouse gas fluxes, and economic feasibility were beyond its scope. Still, after nine years of monitoring, the message from Bundelkhand is unusually clear: the humblest of crops, a well-chosen perennial grass, may be among the cheapest and most effective tools humanity has for putting carbon, fertility, and life back into exhausted soil.</p>
<p><strong>Subject of Research:</strong> Long-term comparative evaluation of perennial grass species for restoring soil carbon and fertility in degraded semi-arid agroecosystems under rainfed and irrigated conditions</p>
<p><strong>Article Title:</strong> Comparative assessment of perennial grasses for restoring degraded semi-arid agroecosystems under contrasting moisture regimes</p>
<p><strong>Article References:</strong> Choudhary, M., Prasad, M., Dixit, A. K., Kantwa, S. R., Mahawer, S. K., &amp; Palsaniya, D. R. (2026). Comparative assessment of perennial grasses for restoring degraded semi-arid agroecosystems under contrasting moisture regimes. <em>Discover Soil, 3</em>(1), Article 182. <a href="https://doi.org/10.1007/s44378-026-00342-6" rel="noopener noreferrer">https://doi.org/10.1007/s44378-026-00342-6</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44378-026-00342-6" rel="noopener noreferrer">10.1007/s44378-026-00342-6</a></p>
<p><strong>Keywords:</strong> perennial grasses, soil restoration, soil organic carbon, semi-arid agroecosystems, carbon management index, restoration efficiency index, guinea grass, land degradation, soil microbial biomass, irrigation, fodder productivity, Bundelkhand</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">244329</post-id>	</item>
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