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	<title>global &#8211; Science</title>
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	<title>global &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>Hidden Moss Worlds Thrive on China&#8217;s Degraded Karst Landscapes</title>
		<link>https://scienmag.com/hidden-moss-worlds-thrive-on-chinas-degraded-karst-landscapes/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Mon, 21 Sep 2026 01:05:53 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[adaptation of biocrusts in humid vs arid regions]]></category>
		<category><![CDATA[biogeography]]></category>
		<category><![CDATA[biological soil crusts]]></category>
		<category><![CDATA[Biological soil crusts in Chinese karst landscapes]]></category>
		<category><![CDATA[community assembly]]></category>
		<category><![CDATA[Cyanobacteria]]></category>
		<category><![CDATA[ecological significance of biocrusts in China]]></category>
		<category><![CDATA[ecosystem restoration]]></category>
		<category><![CDATA[effects of rocky desertification on soil ecosystems]]></category>
		<category><![CDATA[environmental filtering]]></category>
		<category><![CDATA[global]]></category>
		<category><![CDATA[Guizhou]]></category>
		<category><![CDATA[Hyophila rosea]]></category>
		<category><![CDATA[impact of land degradation on soil stabilization]]></category>
		<category><![CDATA[karst ecosystems]]></category>
		<category><![CDATA[land-use pressure on karst ecosystems]]></category>
		<category><![CDATA[moss and lichen communities in humid regions]]></category>
		<category><![CDATA[mosses]]></category>
		<category><![CDATA[Plant Biosystems]]></category>
		<category><![CDATA[rocky desertification]]></category>
		<category><![CDATA[role of cyanobacteria in soil nutrient fixation]]></category>
		<category><![CDATA[soil crust composition in Guizhou Province]]></category>
		<category><![CDATA[species diversity of biocrusts in subtropical environments]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=204864</guid>

					<description><![CDATA[A new survey of Guizhou's degraded karst landscapes reveals moss-dominated biological soil crusts that are taxonomically distinct from the world's dryland crusts.]]></description>
										<content:encoded><![CDATA[<p>Beneath the cracked, chalky surfaces of southern China&#8217;s degraded karst terrain, an unexpected biological empire has been quietly holding the ground together. A new study of biological soil crusts—thin, living skins of mosses, lichens, algae, and cyanobacteria that bind soil particles at the land surface—reveals that these communities in Guizhou Province are strikingly different from their celebrated dryland counterparts. Published in Plant Biosystems, the research offers the most comprehensive species-level portrait yet of biocrusts in the South China Karst, a region where centuries of land-use pressure and soluble carbonate bedrock have produced some of the most severe rocky desertification on Earth.</p>
<p>Biological soil crusts are among the most studied living surfaces in arid and semi-arid environments, where they stabilize soils, fix carbon and nitrogen, and modulate water infiltration across millions of square kilometers. Yet the subtropical humid karst landscapes of Guizhou have remained a conspicuous gap in this global picture. Unlike deserts, these humid regions receive abundant rainfall and support dense vegetation mosaics, raising questions about whether biocrusts even form meaningful communities there, and if so, which species assemble them and why. The new study set out to answer precisely those questions by surveying six representative areas spanning a gradient of ecosystem degradation across the province.</p>
<p>The findings are taxonomically striking. Across all six study areas, the researchers documented 22 distinct biocrust species drawn from four major phyla. Mosses led the roster with 12 species spanning six families and nine genera, followed by eight algal and cyanobacterial species from six families and seven genera, and two lichen species from the phylum Ascomycota. Within the algal component, cyanobacteria dominated heavily, accounting for six species against only two green algae. This asymmetry hints that nitrogen-fixing, stress-tolerant cyanobacteria play a foundational role in these humid, calcium-rich soils, much as they do at the earliest successional stages of crust development in drylands.</p>
<p>But it is the mosses that rule the surface. In every area surveyed, mosses were the absolute dominant crust type, contributing between 75 and 100 percent of total biocrust cover. At the heart of this dominance sits a single, remarkably persistent species: Hyophila rosea, an acrocarpous moss that emerged as the ubiquitous dominant across the entire degradation gradient. Whether a site was lightly disturbed or profoundly degraded, H. rosea held its ground, a biological constant in landscapes otherwise defined by change. Its closest co-dominants, Brachymenium exile and Trichostomum brachydontium, share a similar profile of extremotolerance—traits that allow these diminutive plants to endure the thin soils, high calcium concentrations, and episodic desiccation that define karst surfaces.</p>
<p>Not every moss in these communities is a hardened local specialist. The cosmopolitan silvergreen bryum moss, Bryum argenteum, appeared as an associated, gap-filling taxon, exploiting bare patches between the dominants rather than anchoring the community itself. This division of labor—resilient local specialists forming the structural backbone while widespread opportunists fill the interstices—offers a textbook illustration of how habitat filtering and dispersal dynamics jointly shape community assembly. In karst environments, where soil calcium acts as a well-documented environmental filter, only lineages with tolerance for calcareous, drought-prone microhabitats can persist, and the species list reflects that pruning with unusual clarity.</p>
<p>The study also uncovered a strong spatial signature in where biocrusts thrive. Rather than spreading evenly across the landscape, the crusts showed pronounced habitat preferences, becoming notably enriched in managed groves such as plantations of Zanthoxylum bungeanum, the Sichuan pepper tree, and Camellia oleifera, the oil-tea camellia. By contrast, croplands and natural grasslands supported far less crust development. The pattern makes ecological sense: managed groves experience less frequent mechanical disturbance than cultivated fields, while their canopy structure moderates temperature and moisture extremes at the soil surface in ways that open grasslands do not. Human management, in other words, is not merely degrading these landscapes—it can actively create refugia for the very organisms that aid recovery.</p>
<p>Perhaps the most consequential result emerges from the study&#8217;s global comparison. When the team overlapped its species list with the extensive biocrust literature from the world&#8217;s drylands, the taxonomic overlap proved vanishingly small—less than five percent. Nearly everything living in these Guizhou crusts is different from what lives in desert crusts elsewhere on the planet. Only one cyanobacterial species, the globally widespread Nostoc commune, bridged the two worlds. Every other cyanobacterial and algal species identified in the karst study sites was exclusive to these habitats. Such profound biogeographic differentiation suggests that the prevailing scientific emphasis on dryland biocrusts has, until now, left an entire class of humid-climate crust ecosystems essentially unclassified.</p>
<p>Why does this matter beyond taxonomy? Biocrusts are increasingly recognized as engineers of ecosystem function, and karst landscapes are in desperate need of engineering. Rocky desertification—the exposure of barren carbonate bedrock following soil erosion—degrades water retention, carbon storage, and agricultural productivity across millions of hectares in southwestern China. Prior work by overlapping research groups has shown that moss-dominated crusts in these landscapes modulate soil nitrogen, influence microbial communities, and alter enzyme activities, with effects that vary along degradation gradients. Knowing precisely which species build the crusts provides the species-level baseline required to move from description to intervention: restoration practitioners can now identify, cultivate, and transplant the actual organisms best adapted to the harshest karst conditions.</p>
<p>The study&#8217;s implications also run in the opposite direction. As global change reshapes disturbance regimes, humid-region biocrusts may prove more vulnerable than their desert-adapted relatives, which have evolved under chronic water stress. Understanding which species anchor crust cover in managed groves—and why agricultural and grassland settings suppress them—gives land managers in Guizhou a concrete tool for steering vegetation recovery. A system in which H. rosea and its co-dominants can be encouraged on the right land uses, and shielded on the wrong ones, transforms a minute layer of the biosphere into a lever for landscape-scale rehabilitation.</p>
<p>For a layer of life often dismissed as a smear of green on stone, the biological soil crusts of Guizhou have now been given a name, a roster, and an ecological identity all their own. Twenty-two species, one indispensable moss, and a community unlike any other on Earth: the living skin of China&#8217;s karst is no longer an anonymous footnote to dryland science, but a distinct biogeographic province in its own right—one whose guardians may hold the keys to healing one of the world&#8217;s most degraded terrains.</p>
<p><strong>Subject of Research:</strong> Species composition and community assembly of biological soil crusts in degraded subtropical karst ecosystems of Guizhou, China</p>
<p><strong>Article Title:</strong> Species composition and community assembly characteristics of biological soil crusts in degraded karst ecosystems of Guizhou, China</p>
<p><strong>Article References:</strong> Liu, J., Zhao, X., Deng, M., Zhang, F., Wu, Q., Liu, R., Long, M., &amp; Li, X. (2026). Species composition and community assembly characteristics of biological soil crusts in degraded karst ecosystems of Guizhou, China. <em>Plant Biosystems, 160</em>(5), Article 249. <a href="https://doi.org/10.1007/s44473-026-00257-8" rel="noopener noreferrer">https://doi.org/10.1007/s44473-026-00257-8</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44473-026-00257-8" rel="noopener noreferrer">10.1007/s44473-026-00257-8</a></p>
<p><strong>Keywords:</strong> biological soil crusts, karst ecosystems, mosses, cyanobacteria, rocky desertification, Guizhou, community assembly, environmental filtering, Hyophila rosea, ecosystem restoration, biogeography, Plant Biosystems</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">204864</post-id>	</item>
		<item>
		<title>Selenium Spray Supercharges Antioxidant-Rich Chinese Dwarf Cherry Fruit</title>
		<link>https://scienmag.com/selenium-spray-supercharges-antioxidant-rich-chinese-dwarf-cherry-fruit/</link>
		
		<dc:creator><![CDATA[Daisy Hatcher]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 21:46:51 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[anthocyanins]]></category>
		<category><![CDATA[antioxidant capacity]]></category>
		<category><![CDATA[antioxidant enhancement through foliar spray]]></category>
		<category><![CDATA[Cerasus humilis]]></category>
		<category><![CDATA[Chinese dwarf cherry]]></category>
		<category><![CDATA[flavonoid biosynthesis]]></category>
		<category><![CDATA[flavonoids and anthocyanins in fruit nutrition]]></category>
		<category><![CDATA[foliar spray]]></category>
		<category><![CDATA[fruit quality]]></category>
		<category><![CDATA[genetic mechanisms of selenium-induced metabolic changes]]></category>
		<category><![CDATA[global]]></category>
		<category><![CDATA[health benefits of selenium-rich fruits]]></category>
		<category><![CDATA[impact of trace elements on fruit antioxidant capacity]]></category>
		<category><![CDATA[low-cost strategies for micronutrient enrichment]]></category>
		<category><![CDATA[organic selenium]]></category>
		<category><![CDATA[phenylpropanoid pathway]]></category>
		<category><![CDATA[role of selenium in plant secondary metabolism]]></category>
		<category><![CDATA[selenium biofortification]]></category>
		<category><![CDATA[Selenium biofortification in Chinese dwarf cherry]]></category>
		<category><![CDATA[selenium's role in plant stress response and ripening]]></category>
		<category><![CDATA[sodium selenite]]></category>
		<category><![CDATA[transcriptome analysis]]></category>
		<category><![CDATA[transcriptome analysis of selenium-treated plants]]></category>
		<category><![CDATA[underutilized Chinese fruits with bioactive compounds]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=198796</guid>

					<description><![CDATA[A new study shows that foliar sodium selenite sprays at 120 mg per liter boost selenium content, antioxidant capacity, and flavonoid biosynthesis in Chinese dwarf cherry fruit.]]></description>
										<content:encoded><![CDATA[<p>A single trace element, applied as a simple foliar spray at just the right moments of fruit development, can transform the nutritional profile of one of China&#8217;s most promising underutilized fruits, according to new research published in the journal Plant and Soil. The study, conducted by a team at Shanxi Agricultural University in collaboration with Universiti Teknologi Malaysia, demonstrates that spraying sodium selenite onto Chinese dwarf cherry (Cerasus humilis) trees significantly boosts the fruit&#8217;s selenium content, antioxidant capacity, and levels of health-promoting flavonoids and anthocyanins. The findings offer a practical, low-cost strategy for selenium biofortification of a fruit that is already prized for its dense concentration of bioactive compounds, while also revealing, through transcriptome analysis, the genetic machinery that selenium recruits to rewire the fruit&#8217;s secondary metabolism.</p>
<p>Selenium occupies a curious position in plant biology. It is not considered an essential element for higher plants, yet it functions as a cofactor for a suite of antioxidant enzymes, including the glutathione peroxidases, and it participates in secondary metabolism, stress responses, and the ripening process. For humans, the picture is clearer: selenium is an essential micronutrient, and deficiency affects an estimated one billion people worldwide, with consequences ranging from compromised immune function to increased oxidative stress. Because dietary selenium intake depends heavily on the selenium content of soils where crops are grown, agronomic biofortification—enriching food crops with selenium through fertilization—has emerged as a major strategy in global nutrition efforts. Foliar spraying, in which a selenium solution is applied directly to leaves and developing fruit, is particularly attractive because it bypasses the complex soil chemistry that often locks selenium into unavailable forms and allows precise control over dose and timing.</p>
<p>The Chinese dwarf cherry, known in China as Oula Li, is a small drupe native to northern China that has attracted growing scientific and commercial attention. Despite its modest size, the fruit accumulates remarkable levels of phenolic compounds, flavonoids, anthocyanins, and vitamin C, and previous studies have documented substantial genotypic diversity in its antioxidant capacity. It is also valued for its calcium content and has been the subject of metabolomic investigations into its organic acid composition. Yet until now, no comprehensive study had examined how exogenous selenium application affects the fruit&#8217;s quality, selenium accumulation, or the underlying gene expression programs that govern its flavonoid biosynthesis.</p>
<p>To fill this gap, the research team sprayed &#8216;Jinou-2&#8217; Chinese dwarf cherry trees with sodium selenite solutions ranging from 0 to 150 milligrams per liter, applying the treatments at two critical developmental windows: the young fruit stage and the fruit expansion stage. These stages were chosen because they represent periods of intense cell division and resource allocation, when the fruit&#8217;s metabolic machinery is most responsive to external inputs. After treatment, the researchers measured a battery of fruit quality parameters, including fruit size, peel coloration, soluble solids, organic acid and ascorbic acid content, selenium concentration and speciation, flavonoid and anthocyanin levels, and overall antioxidant activity. They then performed transcriptome sequencing on treated and untreated fruit to identify the genes and pathways responding to selenium.</p>
<p>The results were strikingly dose-dependent. At 120 milligrams per liter, sodium selenite produced the most remarkable improvements across nearly every quality metric. Fruits were larger, their peels displayed deeper redness—an indicator of anthocyanin accumulation—and their flavor profile improved. Critically, the treatment shifted the speciation of selenium within the fruit: the proportion of organic selenium rose while inorganic selenium declined. This shift matters enormously from a nutritional and safety standpoint. Organic selenium compounds, such as selenomethionine incorporated into proteins, are generally more bioavailable and less toxic than inorganic selenite or selenate, so a fruit that converts absorbed inorganic selenium into organic forms delivers a safer and more effective nutritional payload.</p>
<p>Alongside the selenium transformation, the treated fruits showed significantly enhanced antioxidant activity, accompanied by marked increases in ascorbic acid, total flavonoids, and anthocyanins. These compounds form the chemical backbone of the fruit&#8217;s health-promoting reputation, and their coordinated elevation suggests that selenium acts not merely as a passive accumulator but as an active elicitor of secondary metabolism. However, the benefits were not unlimited. When the spray concentration was pushed to 150 milligrams per liter, the positive effects attenuated, indicating that excessive selenium crosses a threshold where it begins to impose stress on the plant rather than support it. This biphasic response—stimulation at moderate doses, inhibition at high doses—is a well-recognized feature of selenium biology and underscores the importance of precise dosing in any biofortification program.</p>
<p>The transcriptome analysis provided the mechanistic depth that elevates the study beyond simple agronomy. Sequencing revealed that the differentially expressed genes between selenium-treated and control fruits were predominantly enriched in the phenylpropanoid and flavonoid biosynthesis pathways. The phenylpropanoid pathway is the metabolic superhighway of plant secondary chemistry: it begins with the amino acid phenylalanine and branches into an enormous diversity of compounds, including lignins, flavonoids, and anthocyanins, many of which serve as antioxidants, pigments, and defense molecules. The finding that selenium treatment upregulates genes in these pathways, and that this transcriptional shift correlates consistently with the measured increases in flavonoid and anthocyanin content, provides a coherent causal narrative: selenium signals the fruit to invest more heavily in its antioxidant chemical arsenal, and the genes encoding the biosynthetic enzymes respond accordingly.</p>
<p>This mechanism resonates with a growing body of literature on selenium&#8217;s elicitor-like effects across horticultural crops. Foliar selenium applications have been shown to enhance anthocyanin biosynthesis in purple lettuce, activate phenylpropanoid metabolism in peach, improve quality and nutrient profiles in citrus, blueberries, strawberries, pomegranate, kiwifruit, and table grapes, and modulate postharvest quality in apples. What the new study adds is a complete chain of evidence—from field application through fruit chemistry to gene expression—in a fruit species that had not previously been examined in this context. The consistency of the transcriptomic data with the biochemical measurements strengthens the conclusion that the flavonoid pathway is a genuine target of selenium signaling in Cerasus humilis, rather than an incidental correlation.</p>
<p>The practical implications are considerable. For growers of Chinese dwarf cherry, the study offers a targeted cultivation protocol: foliar spraying of 120 milligrams per liter sodium selenite at the young fruit and fruit expansion stages provides selenium biofortification and quality enhancement simultaneously, without genetic modification, without altering the crop, and with an input cost measured in pennies per tree. For nutrition policy, it demonstrates that selenium-deficient regions could potentially address local micronutrient gaps by fortifying locally adapted fruit crops rather than relying exclusively on staple cereals. And for the broader field of biofortification research, the study reinforces the emerging view that selenium is not just a nutrient to be accumulated but a metabolic lever that can be pulled to enhance the nutraceutical value of foods.</p>
<p>The authors are appropriately cautious about scaling up. Their conclusions apply to the &#8216;Jinou-2&#8217; cultivar under the single-site field conditions of this study, and they emphasize that multi-site verification is required before large-scale popularization. Cultivar-specific responses, regional soil and climate variations, and the cumulative selenium load in orchard ecosystems all warrant further investigation. Nevertheless, the study marks a significant step forward in the science of fruit biofortification, showing that with a precisely timed spray of a simple selenium salt, a small cherry with an outsized nutritional reputation can be made even more remarkable—one gene, one flavonoid, and one harvest at a time.</p>
<p><strong>Subject of Research:</strong> Foliar selenium biofortification and flavonoid metabolism in Cerasus humilis fruit</p>
<p><strong>Article Title:</strong> Foliar selenium spray enhances selenium content, antioxidant capacity and flavonoid metabolic pathway in Cerasus humilis fruit</p>
<p><strong>Article References:</strong> Lv, J., Liu, N., Dang, Y., Jia, L., Zhang, S., Wang, P., Lee, C. T., Mu, X., &amp; Zhang, J. (2026). Foliar selenium spray enhances selenium content, antioxidant capacity and flavonoid metabolic pathway in Cerasus humilis fruit. <em>Plant and Soil</em>. <a href="https://doi.org/10.1007/s11104-026-09097-z" rel="noopener noreferrer">https://doi.org/10.1007/s11104-026-09097-z</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s11104-026-09097-z" rel="noopener noreferrer">10.1007/s11104-026-09097-z</a></p>
<p><strong>Keywords:</strong> selenium biofortification, Cerasus humilis, Chinese dwarf cherry, sodium selenite, flavonoid biosynthesis, anthocyanins, antioxidant capacity, phenylpropanoid pathway, transcriptome analysis, fruit quality, organic selenium, foliar spray</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">198796</post-id>	</item>
		<item>
		<title>Brain-Wide Activity Ties Subcortical Decline to Spreading Tau in Early Alzheimer&#8217;s</title>
		<link>https://scienmag.com/brain-wide-activity-ties-subcortical-decline-to-spreading-tau-in-early-alzheimers/</link>
		
		<dc:creator><![CDATA[Cassandra Pierce]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 19:50:51 +0000</pubDate>
				<category><![CDATA[Medicine]]></category>
		<category><![CDATA[Alzheimer's disease]]></category>
		<category><![CDATA[Alzheimer's disease progression]]></category>
		<category><![CDATA[Biomarkers]]></category>
		<category><![CDATA[Braak stages]]></category>
		<category><![CDATA[Braak staging of tau pathology]]></category>
		<category><![CDATA[brain]]></category>
		<category><![CDATA[brain-wide activity patterns]]></category>
		<category><![CDATA[cortex]]></category>
		<category><![CDATA[early Alzheimer's biomarkers]]></category>
		<category><![CDATA[global]]></category>
		<category><![CDATA[global brain activity]]></category>
		<category><![CDATA[global brain activity analysis]]></category>
		<category><![CDATA[impact of tau on neuronal loss]]></category>
		<category><![CDATA[Nature Communications.]]></category>
		<category><![CDATA[neurodegeneration]]></category>
		<category><![CDATA[neurofibrillary tangles]]></category>
		<category><![CDATA[neuroimaging]]></category>
		<category><![CDATA[subcortical brain degeneration]]></category>
		<category><![CDATA[subcortical degeneration]]></category>
		<category><![CDATA[subcortical involvement in Alzheimer's]]></category>
		<category><![CDATA[subcortical-cortical degeneration linkage]]></category>
		<category><![CDATA[tau accumulation in hippocampus]]></category>
		<category><![CDATA[tau pathology]]></category>
		<category><![CDATA[tau protein spread]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=198088</guid>

					<description><![CDATA[New research in Nature Communications shows that degeneration in deep subcortical brain regions becomes progressively linked to cortical tau accumulation across Braak stages during early Alzheimer's disease.]]></description>
										<content:encoded><![CDATA[<p>Alzheimer&#8217;s disease has long been portrayed as a story written in the cortex, the wrinkled outer layer of the brain where memory and thought reside. But a new study published in Nature Communications suggests that the opening chapters of that story may be unfolding deeper, in the evolutionarily ancient structures buried beneath the cortical surface. By analyzing global patterns of brain activity, the researchers show that degeneration in subcortical regions is progressively linked to the accumulation of tau protein in the cortex, and that this coupling strengthens as patients move through the earliest stages of the disease.</p>
<p>The research focuses on tau, one of the two hallmark proteins of Alzheimer&#8217;s pathology. Tau accumulates inside neurons in a remarkably stereotyped sequence, first appearing in the transentorhinal region, then spreading through the hippocampal formation and association cortices in a progression that pathologists have catalogued for decades as Braak stages. Neurofibrillary tangles of tau are closely correlated with neuronal loss and cognitive decline, which is why imaging tau in living brains has become one of the most actively pursued goals in dementia research.</p>
<p>What has remained less clear is how this cortical tau burden relates to the well-documented degeneration of subcortical structures such as the thalamus, basal ganglia, and brainstem nuclei. These deep gray matter regions are not passive bystanders in Alzheimer&#8217;s disease. Postmortem studies repeatedly find tau pathology and neuronal loss in structures like the locus coeruleus and the nucleus basalis, which send widespread projections throughout the cortex and are among the earliest sites of pathological change. Yet the functional relationship between subcortical damage and cortical tau spread has been difficult to quantify in living patients.</p>
<p>The new work addresses that gap by treating the brain as a single integrated dynamical system rather than a collection of independent regions. Using resting-state functional imaging, the team derived measures of global brain activity, capturing how fluctuations in neural signaling are coordinated across the entire organ. Instead of examining the cortex and the subcortex in isolation, the analysis explicitly tested whether the strength of global activity coupling changes systematically across Braak-defined regions as Alzheimer&#8217;s progresses from preclinical stages through mild cognitive impairment.</p>
<p>The results reveal a clear progressive pattern. In individuals without measurable tau pathology, the functional dialogue between subcortical structures and the cortex follows a relatively stable organization. But as tau begins to accumulate in the transentorhinal and limbic regions, defined by the early Braak stages, the relationship shifts. Degeneration in subcortical gray matter becomes increasingly tied to global activity measures, and this linkage intensifies as tau advances into neocortical association areas in later preclinical and early symptomatic stages.</p>
<p>Crucially, the progression is spatially organized. The researchers found that the strength of the subcortical-cortical coupling tracked the sequential involvement of Braak regions, meaning that the deepest subcortical degeneration was most strongly associated with tau burden in precisely those cortical areas known to be affected at each stage. This staged correspondence argues against the idea that subcortical atrophy is merely a nonspecific consequence of overall disease severity. Instead, it suggests a mechanistic relationship in which damage to deep nuclei that broadly innervate the cortex may influence, or at least mirror, the regional vulnerability of the cortex to tau.</p>
<p>One plausible biological interpretation involves the cholinergic and noradrenergic systems. The nucleus basalis of Meynert, located in the basal forebrain, supplies acetylcholine to the entire cortical mantle, while the locus coeruleus in the brainstem provides norepinephrine with an even wider reach. Both systems are compromised early in Alzheimer&#8217;s disease, and both play roles in regulating neural activity, arousal, and the cellular stress responses that govern tau phosphorylation. A failing subcortical modulatory system could plausibly alter cortical network dynamics in ways that create conditions favorable to tau aggregation and spread along existing anatomical connections.</p>
<p>The study&#8217;s use of global brain activity as an integrative marker also carries methodological significance. Standard analyses often average activity within predefined regions of interest, which can obscure distributed phenomena. By characterizing whole-brain signal properties, the researchers captured a systems-level signature of disease progression that single-region measures would miss. This approach aligns with a growing recognition, driven by large-scale neuroimaging consortia, that Alzheimer&#8217;s disease is fundamentally a network disorder, with pathology propagating along functional and structural connections rather than emerging randomly across the brain.</p>
<p>The clinical implications are potentially substantial. If subcortical degeneration and global activity disruption can be measured reliably in the preclinical window, they may serve as early indicators of impending cortical tau spread, complementing existing PET-based tau imaging and cerebrospinal fluid biomarkers. Because subcortical structures can be quantified with widely available MRI sequences, a systems-level marker derived from standard scans could extend the reach of early detection to clinical settings where advanced PET imaging is not accessible, and could provide sensitive outcome measures for trials of anti-tau therapies targeting the earliest disease stages.</p>
<p>The findings also reframe the conceptual geography of Alzheimer&#8217;s disease. Rather than a cortical illness with subcortical complications, the condition increasingly appears as a whole-brain process in which deep nuclei and the cortex deteriorate in a coordinated, staged fashion. Understanding the direction of causality, whether subcortical dysfunction actively promotes cortical tau spread or both reflect a shared upstream trigger, remains the central open question. Longitudinal studies combining serial tau PET, structural imaging of subcortical nuclei, and global activity mapping in the same individuals will be essential to answer it. For now, the study adds a compelling piece of evidence that the brain operates as an integrated system in health and in disease, and that the seeds of cortical destruction in Alzheimer&#8217;s may be nourished from below.</p>
<p><strong>Subject of Research:</strong> Progressive coupling of subcortical degeneration and cortical tau spread across Braak regions in early Alzheimer&#x27;s disease measured by global brain activity</p>
<p><strong>Article Title:</strong> Global brain activity links subcortical degeneration to cortical tau progressively across Braak regions over early Alzheimer’s disease stages</p>
<p><strong>Article References:</strong> Mao, Y., Pan, B., &amp; Liu, X. (2026). Global brain activity links subcortical degeneration to cortical tau progressively across Braak regions over early Alzheimer’s disease stages. <em>Nature Communications</em>. <a href="https://doi.org/10.1038/s41467-026-77748-x" rel="noopener noreferrer">https://doi.org/10.1038/s41467-026-77748-x</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1038/s41467-026-77748-x" rel="noopener noreferrer">10.1038/s41467-026-77748-x</a></p>
<p><strong>Keywords:</strong> Alzheimer&#x27;s disease, tau pathology, Braak stages, subcortical degeneration, global brain activity, neuroimaging, cortex, biomarkers, neurodegeneration, Nature Communications, Global, brain</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">198088</post-id>	</item>
		<item>
		<title>Two Decades of Data Reveal Central Indian Forests Flipping From Carbon Sinks to Sources</title>
		<link>https://scienmag.com/two-decades-of-data-reveal-central-indian-forests-flipping-from-carbon-sinks-to-sources/</link>
		
		<dc:creator><![CDATA[Violet Maxwell]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 15:21:38 +0000</pubDate>
				<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[analysis of forest degradation and reforestation patterns]]></category>
		<category><![CDATA[carbon sequestration]]></category>
		<category><![CDATA[Central India]]></category>
		<category><![CDATA[Central Indian forests carbon sink to source transition]]></category>
		<category><![CDATA[climate change]]></category>
		<category><![CDATA[community forest rights]]></category>
		<category><![CDATA[deforestation]]></category>
		<category><![CDATA[dry deciduous forests]]></category>
		<category><![CDATA[ecological sensitivity of Central Indian forests]]></category>
		<category><![CDATA[effects of deforestation and climate change on Indian tropical forests]]></category>
		<category><![CDATA[forest carbon dynamics]]></category>
		<category><![CDATA[global]]></category>
		<category><![CDATA[impact of dry and moist deciduous forests on carbon cycle]]></category>
		<category><![CDATA[implications for India's climate commitments and carbon budget]]></category>
		<category><![CDATA[India State of Forest Report]]></category>
		<category><![CDATA[long-term trends in forest carbon sequestration in Central India]]></category>
		<category><![CDATA[REDD+]]></category>
		<category><![CDATA[role of forest management in carbon flux changes]]></category>
		<category><![CDATA[significance of 20-year forest carbon loss data]]></category>
		<category><![CDATA[soil organic carbon]]></category>
		<category><![CDATA[sustainable forest management]]></category>
		<category><![CDATA[systematic review]]></category>
		<category><![CDATA[systematic review of forest carbon dynamics in India]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=195823</guid>

					<description><![CDATA[A systematic review of 223 studies published between 2005 and 2025 finds that Central India's tropical forests may be shifting from net carbon sinks to net carbon sources, with a recorded net loss of 59 gigagrams of carbon driven by deforestation, degradation, fire and climate stress.]]></description>
										<content:encoded><![CDATA[<p>The forests of Central India have long been counted among the quiet workhorses of the global carbon cycle, pulling carbon dioxide from the atmosphere through photosynthesis and locking it away in tree trunks, roots and soils. A sweeping new synthesis of two decades of research, however, suggests that this reliability can no longer be assumed. A systematic review consolidating 223 studies published between 2005 and 2025 finds that parts of Central India, a region dominated by ecologically sensitive dry and moist deciduous forests, may be transitioning from net carbon sinks toward net carbon sources, with a recorded net loss of 59 gigagrams of carbon over the last twenty years. The finding, published in the open-access journal Discover Forests, carries uncomfortable implications for India&#8217;s climate commitments and for the health of one of the world&#8217;s largest tracts of tropical forest.</p>
<p>The review, led by Shishir Chandrakar and Krishna Kumar Chandra of Guru Ghasidas Vishwavidyalaya together with Bhavana Dixit of Chhattisgarh Rajya Niti Aayog, is deliberately framed as a critical synthesis rather than a new empirical study. The authors screened more than 90,000 records from Web of Science, Scopus and Google Scholar, narrowing these through duplicate removal, title and abstract screening, and full-text assessment to a final pool of 223 publications meeting rigorous methodological criteria. The twenty-year window they define as long-term is not arbitrary: it spans four assessment cycles of the India State of Forest Report, covers the entire post-2005 period against which India&#8217;s Nationally Determined Contributions and forest-carbon pledges are tracked, and is long enough to capture slow processes such as soil organic carbon turnover and stand-level biomass accumulation that shorter studies simply cannot resolve.</p>
<p>The technical picture that emerges is one of enormous variability and genuine alarm. Aboveground biomass carbon in Central Indian forests fluctuated between 26.4 and 131.1 megagrams of carbon per hectare across the reviewed studies, while soil organic carbon stocks ranged from 24.6 to 50.2 megagrams per hectare. Total biomass in some landscapes reached 338.3 megagrams per hectare, and closed natural forests held considerably more carbon, around 208.22 megagrams per hectare, than open forests at roughly 95.11. Intact stands of mixed sal and teak performed best, and carbon stock densities across various forest types spanned roughly 50 to 180 megagrams per hectare, depending on tree density, species diversity, age structure and management history. These ranges matter because carbon accounting schemes, carbon markets and national inventories all depend on knowing how much carbon a given hectare actually stores.</p>
<p>What makes the findings striking is the disconnect they reveal between national aggregates and regional reality. Nationally, Indian forests remain recognised as vital carbon sinks, holding an estimated 7,124 million tonnes of carbon, and national reports recorded a net increase of 377 million tonnes of carbon between 1995 and 2005. Yet the granular, site-level evidence compiled in this review shows that vulnerable ecosystems in Central India are actively degrading and releasing carbon even as headline statistics improve. In one disturbed tropical forest landscape, approximately 1,851.8 hectares were lost between 2000 and 2020, largely to agricultural conversion, producing a net loss of 0.065 teragrams of biomass and roughly 59 gigagrams of carbon, equivalent to about 216 gigagrams of carbon dioxide. National averages, the authors argue, may be masking precisely the localised declines that matter most for conservation and climate policy.</p>
<p>The drivers of this carbon loss are neither mysterious nor singular. Deforestation driven by agricultural expansion, mining, urbanisation and infrastructure development remains the dominant force, but the review highlights a web of interacting pressures that together erode carbon stocks. Overgrazing suppresses regeneration and shifts species composition toward lower-biomass stands. Repeated low-intensity fires, many of them human-ignited, kill trees and reduce both biomass and soil carbon availability. Linear infrastructure such as roads and transmission lines fragments habitat and creates edge effects that elevate tree mortality and fire risk. Fuelwood extraction has a long history in the region, with an estimated deficit of 86 million tonnes recorded as far back as 1996, and excessive livestock grazing has stunted forest floor regeneration in around 67 percent of national parks and 83 percent of wildlife sanctuaries. Timber extraction alone accounted for roughly half of degradation in some studied landscapes, followed by fuelwood collection, fires and grazing.</p>
<p>Climate change is compounding, rather than replacing, these anthropogenic pressures. The Intergovernmental Panel on Climate Change projects global temperature rises of 1.5 to 4.5 degrees Celsius alongside doubled atmospheric carbon dioxide by the end of the century, and Central India sits squarely in the crosshairs. Vulnerability assessments rank Chhattisgarh, Madhya Pradesh and Odisha among the most climate-exposed regions in the country. Projections summarised in the review suggest that by 2050, large areas of tropical moist deciduous and semi-evergreen forest, covering some 520,280 square kilometres of India&#8217;s most dominant forest types, will fall within climatic hotspots, facing altered precipitation, elevated temperatures and increased drought and fire. Conflicting model scenarios add to the uncertainty: greenhouse gas forcing models predict warmer and wetter conditions that could boost productivity, while aerosol-inclusive models foresee drier, water-stressed futures that would accelerate the shift from moist to drier forest types.</p>
<p>Perhaps most unsettling is the evidence that extreme climate events can temporarily flip the sign of the regional carbon budget. During drought episodes, plant respiration in Central India&#8217;s deciduous forests has been documented to exceed primary productivity, releasing an estimated 210 million tonnes of carbon annually under those conditions. Drought-linked tree mortality accelerates decay-driven carbon release and raises fire probability, and El Niño-associated droughts globally amplify exactly this pattern. Soils, which hold the largest share of India&#8217;s forest carbon at over 50 percent of total stocks, are particularly exposed: decomposition rates respond directly to warming and shifting moisture, and the review notes a clear decline of soil organic carbon with depth, meaning topsoil degradation translates disproportionately into carbon loss.</p>
<p>The synthesis does not end on a purely pessimistic note, and its prescriptions are unusually concrete. Sustainable forest management, assisted natural regeneration of degraded lands, mixed-species planting with native species, soil moisture conservation, fire-line maintenance and invasive species control all emerge as proven levers for restoring carbon storage. India&#8217;s Nationally Determined Contributions target the sequestration of 2.5 to 3 billion tonnes of additional carbon dioxide and the restoration of 26 million hectares of degraded land by 2030, and the rehabilitation of degraded forests is estimated to offer a further 1,008.49 teragrams of carbon mitigation potential over 75 years. Species diversity itself matters: taxonomic richness and structural diversity correlate strongly with aboveground biomass through niche complementarity, and dominant regional species such as Diospyros melanoxylon, Butea monosperma and Shorea robusta are key carbon contributors. Monoculture plantations, by contrast, typically store less carbon and are more vulnerable to pests and climate extremes, a nuance the authors stress against simplistic area-based afforestation targets.</p>
<p>Community governance emerges as perhaps the decisive variable. Madhya Pradesh holds India&#8217;s largest forest area and second-largest carbon stock at 608 million tonnes, with Chhattisgarh close behind at 505 million tonnes, and both states sit at the heart of the Green India Mission and World Bank-supported Ecosystem Services Improvement Project. Chhattisgarh has been actively financing Community Forest Resource management plans developed by gram sabhas, the village assemblies empowered under the Forest Rights Act. Yet the review documents persistent friction: village councils often struggle to access funds because of complex administrative prerequisites and lingering resistance from state forest departments, while growing investment interest in forest lands for mining, carbon schemes and ecotourism raises concerns about pressure on Adivasi territories. The authors argue that genuine carbon mitigation in Central India hinges on authentic devolution of rights and finance to forest communities rather than on the scale of announced programmes.</p>
<p>Ultimately, the review positions Central India as both a warning and a test bed. The evidence for a region-wide shift to net carbon source status still rests on a limited number of regional studies rather than a dense monitoring network, and the authors are candid that belowground carbon dynamics remain under-sampled and methodological differences across studies complicate comparisons. But the direction of travel is clear enough that the distinction between national gains and regional losses cannot be ignored. Meeting India&#8217;s forest-carbon commitments, the synthesis concludes, will depend less on planting trees across aggregate areas and more on safeguarding the quality, species composition and soil integrity of existing natural forests in Chhattisgarh, Madhya Pradesh and Odisha. The authors call for harmonised long-term monitoring networks that integrate field inventories, remote sensing and soil carbon measurement, calibrated to Forest Survey of India assessment cycles. In a region where ecological sensitivity and socio-economic dependence on forests converge at their most intense, the next two decades will determine whether these landscapes slip further into carbon deficit or recover their role as durable climate allies.</p>
<p><strong>Subject of Research:</strong> Twenty-year synthesis of forest carbon dynamics, stocks and sink-to-source transition in Central Indian tropical forests</p>
<p><strong>Article Title:</strong> A critical synthesis of forest carbon dynamics in central india over two decades</p>
<p><strong>Article References:</strong> Chandrakar, S., Chandra, K. K., &amp; Dixit, B. (2026). A critical synthesis of forest carbon dynamics in central india over two decades. <em>Discover Forests, 2</em>(1), Article 64. <a href="https://doi.org/10.1007/s44415-026-00123-7" rel="noopener noreferrer">https://doi.org/10.1007/s44415-026-00123-7</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44415-026-00123-7" rel="noopener noreferrer">10.1007/s44415-026-00123-7</a></p>
<p><strong>Keywords:</strong> forest carbon dynamics, Central India, carbon sequestration, soil organic carbon, deforestation, REDD+, sustainable forest management, climate change, systematic review, India State of Forest Report, community forest rights, dry deciduous forests</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">195823</post-id>	</item>
		<item>
		<title>Weighing 606 Million Buildings Reveals Stark Global Inequality in Urban Materials</title>
		<link>https://scienmag.com/weighing-606-million-buildings-reveals-stark-global-inequality-in-urban-materials/</link>
		
		<dc:creator><![CDATA[Courtney Benton]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 12:20:58 +0000</pubDate>
				<category><![CDATA[Social Science]]></category>
		<category><![CDATA[buildings]]></category>
		<category><![CDATA[built environment]]></category>
		<category><![CDATA[built environment material analysis]]></category>
		<category><![CDATA[characterization]]></category>
		<category><![CDATA[cities]]></category>
		<category><![CDATA[concrete]]></category>
		<category><![CDATA[environmental footprint of buildings]]></category>
		<category><![CDATA[environmental impact of urban development]]></category>
		<category><![CDATA[global]]></category>
		<category><![CDATA[global building material stock]]></category>
		<category><![CDATA[global construction industry data]]></category>
		<category><![CDATA[global infrastructure material distribution]]></category>
		<category><![CDATA[high-income vs low-income city construction]]></category>
		<category><![CDATA[material efficiency]]></category>
		<category><![CDATA[material intensity in urban areas]]></category>
		<category><![CDATA[material stocks]]></category>
		<category><![CDATA[resource use]]></category>
		<category><![CDATA[structural imbalance in urban infrastructure]]></category>
		<category><![CDATA[Sustainability]]></category>
		<category><![CDATA[sustainability of city materials]]></category>
		<category><![CDATA[urban form]]></category>
		<category><![CDATA[urban inequality]]></category>
		<category><![CDATA[urban material inequality]]></category>
		<category><![CDATA[urbanization and resource consumption]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=194067</guid>

					<description><![CDATA[A building-level global database of 606 million structures finds 835 gigatonnes of materials in use and stark inequalities between high-income and low-income countries.]]></description>
										<content:encoded><![CDATA[<p>Every city on Earth rests on an invisible mountain of stuff. Steel frames, concrete foundations, brick facades, glass curtain walls, timber floors and copper wiring together form what researchers call the built environment&#8217;s material stock, and for the first time scientists have put that mountain on a global scale, building by building. A new analysis published in Nature Cities has assembled a database covering 606 million individual structures and concluded that humanity has locked approximately 835 gigatonnes of materials into its buildings. That staggering figure, equivalent to roughly 110 tonnes for every person alive, is not distributed evenly across the planet. The study&#8217;s most striking finding is that the world&#8217;s building materials are concentrated overwhelmingly in high-income countries, while hundreds of millions of people in low-income regions live in structures that embody only a fraction of the material intensity found in wealthy urban centres. The researchers describe this pattern as urban material inequality, a structural imbalance with profound consequences for both human development and the global environment.</p>
<p>The methodology behind the estimate represents a significant advance in how scientists quantify the physical economy. Rather than extrapolating from sparse national statistics, the team constructed a building-level characterization that records the footprint, height, typology and inferred material composition of individual structures worldwide. By combining machine-learning classification of satellite and geospatial data with engineering relationships that translate a building&#8217;s geometry into mass of concrete, steel, masonry, timber and other materials, the researchers could weight each of the 606 million structures much as an accountant weighs each asset on a balance sheet. The result is a high-resolution global map of where material mass physically sits, from the reinforced concrete towers of East Asian megacities to the low-rise masonry neighbourhoods of Europe and the lightweight dwellings of sub-Saharan Africa.</p>
<p>The headline number, 835 gigatonnes, confirms that buildings dominate the material dimension of human civilization. Earlier work, including a landmark study published in the Proceedings of the National Academy of Sciences in 2017, showed that global socioeconomic material stocks rose twenty-three-fold over the twentieth century and that maintaining and expanding those stocks now requires roughly half of all annual resource use. The new building-level inventory sharpens that picture considerably by showing exactly which objects consume those resources. Buildings, it turns out, are the single largest store of anthropogenic materials, outweighing infrastructure, vehicles and machinery combined by a wide margin. Concrete and aggregate dominate the stock, followed by brick, steel and timber, with the mix varying systematically by region, income level and urban form.</p>
<p>What elevates the study beyond a bookkeeping exercise is its demonstration that material stock correlates strongly with urban form, and that urban form is a policy variable. Dense, compact cities with mid-rise and high-rise construction embody far less material per unit of floor area than sprawling, low-density development built with single-family homes. A detached suburban house may require several times more material per square metre of living space than an apartment in a well-engineered residential tower, because it spreads foundations, walls and roofs across a much larger footprint for the same usable area. The researchers show that cities which have grown vertically, whether in East Asia or in dense European cores, deliver housing and commercial space with markedly higher material efficiency than cities that have grown outward. The choice of urban form made today, in other words, is a choice about how many gigatonnes of stone, sand, iron and cement future generations will need to extract.</p>
<p>The inequality dimension of the findings is likely to spark the most debate. High-income countries hold a disproportionately large share of the global building stock relative to their populations, reflecting decades of accumulated construction, larger per-capita floor areas and heavier material specifications. Low-income countries, by contrast, face an enormous unfinished task: providing adequate housing, schools, clinics and workplaces for growing urban populations with building stocks that are materially thin. A household in a wealthy economy may be sheltered by hundreds of tonnes of embodied material, while a household in a low-income country may live within a structure embodying a fraction of that mass. Closing this material gap is a development imperative, yet it collides head-on with planetary limits, because the cement, steel and aluminium industries already account for a substantial share of global carbon dioxide emissions and industrial energy demand.</p>
<p>This tension frames what the study&#8217;s authors call efficiency paths. If low-income nations simply replicate the material-intensive development trajectories of the twentieth century, the global building stock could balloon in ways that climate targets cannot absorb. But the building-level database suggests alternatives. Material-efficient urban forms, compact neighbourhoods served by shared infrastructure, mid-rise construction that balances density with buildability, and designs that extend structural lifetimes and enable reuse of components, could deliver comparable human wellbeing with dramatically less new material. Scenario analyses published in Nature Communications in 2021 estimated that material-efficiency strategies in residential buildings alone could save billions of tonnes of resources and significant emissions, and the new global inventory provides the granular baseline needed to identify where those strategies would pay off most.</p>
<p>The technical achievement of characterizing 606 million buildings also matters for how cities are managed. Material stocks are not static; they are slow-motion flows. Every year, part of the stock is demolished and replaced, releasing construction and demolition waste, while new construction draws fresh resources from mines, quarries and forests. Knowing where materials are concentrated, how old they are and what they are made of allows planners to treat the existing city as a reservoir, an urban mine whose steel and concrete can be recovered and reused rather than discarded. It also enables more accurate life-cycle assessment, better forecasts of future demolition waste, and more precise carbon accounting, since the emissions embedded in a city&#8217;s buildings can now be estimated structure by structure rather than guessed from national averages.</p>
<p>The study builds on a rapid recent evolution in the field. A 2025 analysis in the Journal of Industrial Ecology produced the first global high-resolution map of building material stocks, and a 2024 study in Engineering used big geodata to reveal spatial patterns of built-environment stocks across and within fifty Chinese cities, showing that material intensity varies not only between countries but dramatically between neighbourhoods of the same city. The new Nature Cities work scales this building-level approach to the entire planet and adds the explicit inequality framing, quantifying the gap between the material abundance of wealthy urban systems and the material scarcity of poorer ones. In doing so, it connects two research communities that have often worked separately: industrial ecologists tracking global resource flows, and urban scientists studying the shape and growth of cities.</p>
<p>The implications reach into international climate negotiations, development finance and urban planning practice alike. For high-income countries, the findings suggest that the priority is not merely reducing new construction but managing an already massive stock efficiently, through renovation, densification, adaptive reuse and circular-economy strategies that keep existing materials in service. For low-income and middle-income countries, the findings argue for infrastructure and housing policies that leapfrog the most material-wasteful development patterns, adopting compact urban forms and efficient construction technologies before car-dependent sprawl and resource-hungry building standards become locked in. The 835 gigatonnes already in the ground cannot be un-built, but the next several hundred tonnes that humanity will inevitably add remain, for now, a choice. The new global inventory of the world&#8217;s buildings makes that choice visible, measurable and, for the first time, mappable at the scale of every structure on Earth.</p>
<p><strong>Subject of Research:</strong> Global building-level quantification of urban material stocks and inequality</p>
<p><strong>Article Title:</strong> Global characterization of building-level weight reveals urban material inequality</p>
<p><strong>Article References:</strong> Global characterization of building-level weight reveals urban material inequality. (2026). <em>Nature Cities</em>. <a href="https://doi.org/10.1038/s44284-026-00509-w" rel="noopener noreferrer">https://doi.org/10.1038/s44284-026-00509-w</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1038/s44284-026-00509-w" rel="noopener noreferrer">10.1038/s44284-026-00509-w</a></p>
<p><strong>Keywords:</strong> material stocks, built environment, urban inequality, buildings, concrete, material efficiency, urban form, sustainability, cities, resource use, Global, characterization</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">194067</post-id>	</item>
		<item>
		<title>Environmental structuring of mixoplankton functional types within marine protist communities: a global analysis</title>
		<link>https://scienmag.com/environmental-structuring-of-mixoplankton-functional-types-within-marine-protist-communities-a-global-analysis/</link>
		
		<dc:creator><![CDATA[Violet Maxwell]]></dc:creator>
		<pubDate>Thu, 03 Sep 2026 20:38:27 +0000</pubDate>
				<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[analysis]]></category>
		<category><![CDATA[communities]]></category>
		<category><![CDATA[DNA metabarcoding of ocean microbes]]></category>
		<category><![CDATA[environmental]]></category>
		<category><![CDATA[environmental drivers of plankton communities]]></category>
		<category><![CDATA[functional]]></category>
		<category><![CDATA[global]]></category>
		<category><![CDATA[global ocean plankton analysis]]></category>
		<category><![CDATA[machine learning in oceanography]]></category>
		<category><![CDATA[marine]]></category>
		<category><![CDATA[marine protist functional types]]></category>
		<category><![CDATA[microbial community structure in oceans]]></category>
		<category><![CDATA[mixoplankton]]></category>
		<category><![CDATA[Mixoplankton distribution]]></category>
		<category><![CDATA[mixotrophic marine microbes]]></category>
		<category><![CDATA[nutrient and temperature gradients in marine ecosystems]]></category>
		<category><![CDATA[ocean microbiome mapping]]></category>
		<category><![CDATA[protist]]></category>
		<category><![CDATA[protist functional diversity]]></category>
		<category><![CDATA[role of mixoplankton in marine food webs]]></category>
		<category><![CDATA[Scientific Research]]></category>
		<category><![CDATA[structuring]]></category>
		<category><![CDATA[types]]></category>
		<category><![CDATA[within]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=186716</guid>

					<description><![CDATA[In the sunlit layers of the world ocean, a remarkable group of microscopic organisms quietly blurs the boundary between plant and animal. Known as mixoplankton, these single-celled protists can both photosynthesize like algae and engulf prey like predators, and a]]></description>
										<content:encoded><![CDATA[<p>In the sunlit layers of the world ocean, a remarkable group of microscopic organisms quietly blurs the boundary between plant and animal. Known as mixoplankton, these single-celled protists can both photosynthesize like algae and engulf prey like predators, and a new global analysis has now mapped, with unprecedented breadth, where each of their distinct functional types lives and why. By combining tens of thousands of DNA sequences from across the planet with machine learning and classical oceanographic statistics, an international research team has shown that these versatile microbes are not ecological curiosities at the margins of marine food webs but ubiquitous, environmentally structured players whose distributions follow temperature, salinity, and nutrient gradients with striking consistency.</p>
<p>The study, published in the journal Ocean Microbiology, drew on the metaPR2 database, a curated collection of processed 18S rRNA gene metabarcodes from more than forty studies spanning thousands of samples worldwide. The researchers classified roughly 47,000 marine protist amplicon sequence variants, or ASVs, into functional categories using the Mixoplankton Database, a resource that catalogues known mixotrophic species and their trophic strategies. Four mixoplankton types emerged as the focus of the analysis: constitutive mixoplankton, which build their own chloroplasts; generalist non-constitutive mixoplankton, which steal chloroplasts from a broad range of prey; plastidic specialist non-constitutive mixoplankton, which selectively retain plastids and even nuclear material from specific prey for weeks or months; and endosymbiotic specialist non-constitutive mixoplankton, which harbor long-term photosynthetic symbionts inside their cells.</p>
<p>These distinctions matter because each strategy carries different physiological costs and ecological consequences. Constitutive mixoplankton, which include familiar dinoflagellate and haptophyte genera such as Alexandrium, Karlodinium, and Karenia, can photosynthesize continuously while opportunistically consuming prey. Generalists of the non-constitutive kind, such as ciliates in the genera Strombidium and Laboea, must feed frequently, on scales of hours to days, because their stolen plastids degrade quickly. Plastidic specialists such as Mesodinium and Dinophysis can maintain sequestered photosynthetic machinery for extended periods, while endosymbiotic specialists like Ornithocercus and the green form of Noctiluca scintillans sustain stable partnerships with algal cells that contribute sugars and recycle nutrients derived from prey digestion.</p>
<p>After filtering the data to euphotic-zone samples, those from the upper 200 meters where light penetrates, the final dataset comprised nearly 44,000 ASVs and more than 366 million reads from 4,190 samples reaching latitudes from roughly 74 degrees south to 89 degrees north. Mixoplankton appeared in 94 percent of the samples, confirming their global ubiquity. Overall, mixoplankton accounted for about 7 percent of protist ASVs, corresponding to 3,537 sequence variants and 192 species, which represents some 44 percent of the species listed in the Mixoplankton Database. Protozooplankton and parasites dominated the ASV counts at 38 and 24 percent respectively, while diatoms made up 8 percent and other phytoplankton 22 percent.</p>
<p>To untangle the patterns hidden within this enormous dataset, the team turned to self-organizing maps, an unsupervised machine learning technique that condenses thousands of ASV abundance profiles into two-dimensional neuronal grids that can then be hierarchically clustered. Because sequencing methodology, particularly the choice between the V4 and V9 hypervariable regions of the 18S rRNA gene and the seawater filtration strategy, strongly shapes recovered community composition, the researchers deliberately analyzed separate subdatasets defined by consistent methods rather than pooling everything together. The clustering, applied independently to three subdatasets, each explained between 75 and 78 percent of total variance and produced community groupings that aligned with four major oceanic biomes: polar, subpolar to temperate, temperate to subtropical, and subtropical to tropical.</p>
<p>Those biome assignments were far from arbitrary. Principal component ordination and temperature-salinity-nitrate diagrams showed that the machine learning clusters ordered themselves consistently along environmental gradients of temperature, salinity, and nitrate concentration, with statistical tests confirming significant differences among clusters. Polar and subpolar communities were associated with the coldest waters and highest nitrate levels, while temperate, subtropical, and tropical communities corresponded with warmer, nutrient-poor conditions. Salinity played a comparatively weaker structural role, likely because it varies over a relatively narrow range in marine waters. The resulting biogeography matched classical oceanographic regions described in earlier plankton studies, lending confidence to the approach.</p>
<p>Within this framework, each mixoplankton functional type revealed its own ecological signature. Constitutive mixoplankton were broadly distributed across all biomes and showed distributional patterns closely paralleling those of non-diatom phytoplankton, suggesting either functional overlap or shared resource use between the two groups. Generalized additive models, which can capture non-linear relationships, showed that constitutive mixoplankton reached high relative abundances across a wide temperature span from near zero to 30 degrees Celsius, typical oceanic salinities, and low nitrate concentrations, consistent with the idea that mixotrophy confers a competitive advantage when dissolved nutrients are scarce. Endosymbiotic specialists, by contrast, were restricted to warmer subpolar through tropical waters and were largely absent from polar regions, with more than 88 percent of their sequence variants in one subdataset belonging to Collodaria, radiolarian colonies characteristic of oligotrophic open oceans.</p>
<p>The remaining two mixotypes were scarcer but ecologically revealing. Generalist non-constitutive mixoplankton, the least abundant group, consistently co-occurred with diatoms and extended into nitrate-rich regimes of 20 to 30 micromolar, echoing their dependence on frequent ingestion of phototrophic prey that flourish in productive waters; they were also detected in upwelling zones such as the equatorial Pacific and the Agulhas Current. Plastidic specialists spanned all biomes but were sparse, and in this study appeared in lower-nutrient conditions than previously reported, a shift the authors attribute to seasonal sampling differences and the capacity of retained plastids to sustain photosynthesis across varying nutrient regimes. Diatoms themselves, the only protists confidently confirmed as strictly phototrophic, were predominantly tied to cold, nitrate-rich waters, while protozooplankton and parasites displayed trends generally inverse to those of the mixoplankton, hinting at partitioned consumer niches and host-driven distributions.</p>
<p>The analysis also exposed how profoundly methodological choices shape what scientists see. Mixoplankton richness and relative abundance were, respectively, threefold and sixfold higher in the V9 dataset than in the V4 dataset, largely because the Tara Oceans V9 data captured radiolarians whose exceptionally high rRNA gene copy numbers are differentially amplified by the two marker regions. Comparisons of samples sequenced with both markers showed roughly 60 percent species overlap and significantly correlated abundances, yet one endosymbiotic radiolarian, Collozoum amoeboides, appeared three orders of magnitude more abundant in V9 than in V4. Filtration strategy added further complications, since fragile cells can be disrupted during size fractionation while unfractionated samples can mask rarer groups. The authors stress that these discrepancies do not undermine the conclusions but underscore the need for careful, method-aware interpretation.</p>
<p>By placing mixoplankton within the full context of marine protistan communities at a global scale, the study delivers the first community-level assessment of mixoplankton biogeography relative to co-occurring functional types, and it establishes an empirical foundation for incorporating these organisms into predictive models of marine ecosystem dynamics. The researchers argue that future work should prioritize targeted detection of the underrepresented generalist and plastidic specialist types, whose sparse detection partly reflects their small numbers of known species and the fragility of their cells, and should embrace emerging transcriptomic machine learning methods that can infer trophic mode from gene expression in field communities. As oceans warm and nutrient cycles shift, knowing which mixoplankton strategies dominate where, and under what environmental conditions, may prove essential for forecasting how marine food webs and biogeochemical cycles will respond.</p>
<p>The recognition of mixoplankton as a distinct ecological category represents a relatively recent shift in plankton science. For much of the twentieth century, marine protists were sorted into a simple dichotomy of phytoplankton and zooplankton, an arrangement that implicitly assumed photosynthesis and phagotrophy were mutually exclusive trophic modes. Observations of planktonic ciliates carrying algal plastids and dinoflagellates consuming prey date back more than a century, but only with the development of trait-based frameworks and curated databases has the full diversity of these strategies become systematically catalogued.</p>
<p>The ecological stakes of this reclassification are considerable. Because mixoplankton can acquire nutrients through both dissolved uptake and prey ingestion, they occupy a flexible position in microbial food webs, capable of acting as primary producers when inorganic nutrients are scarce and as grazers when prey are abundant. This dual capacity influences how carbon and nitrogen move through planktonic communities, and models that omit mixotrophy risk misallocating energy flow and nutrient recycling pathways.</p>
<p>The global niche patterns documented in the study also carry implications for a changing ocean. As surface waters warm and stratification intensifies, nutrient supply to the euphotic zone is expected to decline in many regions, conditions that favor organisms able to supplement photosynthesis with feeding. The observed affinity of constitutive mixoplankton for warm, oligotrophic waters, and of endosymbiotic specialists for tropical and subtropical biomes, suggests that these groups may expand as such conditions become more widespread, potentially reshaping community composition and the efficiency of biological carbon export.</p>
<p>Equally important is the methodological legacy of the work. By demonstrating that marker gene choice and sample processing measurably alter perceived mixoplankton abundance, the analysis provides a cautionary benchmark for future metabarcoding surveys and underscores the value of standardized, method-aware databases for tracking marine biodiversity over time.</p>
<p><strong>Subject of Research:</strong> Environmental structuring of mixoplankton functional types within marine protist communities: a global analysis</p>
<p><strong>Article Title:</strong> Environmental structuring of mixoplankton functional types within marine protist communities: a global analysis</p>
<p><strong>Article References:</strong> Larsson, M. E., Leles, S. G., Mitra, A., Faure, E., Vaulot, D., &amp; Santoferrera, L. (2026). Environmental structuring of mixoplankton functional types within marine protist communities: a global analysis. <em>Ocean Microbiology, 2</em>(1), Article 1. <a href="https://doi.org/10.1186/s44375-026-00007-3" rel="noopener noreferrer">https://doi.org/10.1186/s44375-026-00007-3</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s44375-026-00007-3" rel="noopener noreferrer">10.1186/s44375-026-00007-3</a></p>
<p><strong>Keywords:</strong> Environmental, structuring, mixoplankton, functional, types, within, marine, protist, communities, global, analysis, scientific research</p>
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