<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>ecosystem functioning &#8211; Science</title>
	<atom:link href="https://scienmag.com/tag/ecosystem-functioning/feed/" rel="self" type="application/rss+xml" />
	<link>https://scienmag.com</link>
	<description></description>
	<lastBuildDate>Thu, 24 Sep 2026 00:03:08 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.1.2</generator>

<image>
	<url>https://scienmag.com/wp-content/uploads/2024/07/cropped-scienmag_ico-32x32.jpg</url>
	<title>ecosystem functioning &#8211; Science</title>
	<link>https://scienmag.com</link>
	<width>32</width>
	<height>32</height>
</image> 
<site xmlns="com-wordpress:feed-additions:1">73899611</site>	<item>
		<title>Billions of Marine Worms Move Mountains of Estuary Mud, Study Finds</title>
		<link>https://scienmag.com/billions-of-marine-worms-move-mountains-of-estuary-mud-study-finds/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Thu, 24 Sep 2026 00:03:08 +0000</pubDate>
				<category><![CDATA[Climate]]></category>
		<category><![CDATA[Bahia Brazil estuary study]]></category>
		<category><![CDATA[Bayesian modeling]]></category>
		<category><![CDATA[benthic invertebrate ecosystem functions]]></category>
		<category><![CDATA[bioturbation]]></category>
		<category><![CDATA[conservation]]></category>
		<category><![CDATA[ecological scaling of invertebrate activities]]></category>
		<category><![CDATA[ecosystem functioning]]></category>
		<category><![CDATA[estuarine ecology]]></category>
		<category><![CDATA[estuarine organic matter consumption]]></category>
		<category><![CDATA[functional redundancy]]></category>
		<category><![CDATA[long-term benthic monitoring]]></category>
		<category><![CDATA[macrofauna]]></category>
		<category><![CDATA[Marine worm ecological impact]]></category>
		<category><![CDATA[organic material processing in estuaries]]></category>
		<category><![CDATA[organic matter decomposition]]></category>
		<category><![CDATA[polychaete sediment reworking]]></category>
		<category><![CDATA[polychaetes]]></category>
		<category><![CDATA[role of marine worms in sediment turnover]]></category>
		<category><![CDATA[salinity gradient]]></category>
		<category><![CDATA[sediment displacement by worms]]></category>
		<category><![CDATA[sediment dynamics in estuarine environments]]></category>
		<category><![CDATA[sediment reworking]]></category>
		<category><![CDATA[tropical estuary]]></category>
		<category><![CDATA[tropical estuary biodiversity]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=211498</guid>

					<description><![CDATA[A new study estimates that polychaete worms in a tropical Brazilian estuary consume over 232 tons of organic matter and rework more than 6,000 cubic meters of sediment every four days, revealing how laboratory experiments and long-term monitoring can be combined to quantify ecosystem-level functions.]]></description>
										<content:encoded><![CDATA[<p>Beneath the mudflats of a tropical Brazilian estuary, an army of unassuming marine worms is quietly performing labor on a staggering scale. A new study estimates that polychaetes—bristled segmented worms that most beachgoers never notice—consume roughly 232.6 tons of organic material and rework more than 6,000 cubic meters of sediment every 96 hours across a 23.7 square kilometer stretch of the Jaguaripe River estuary in Bahia, Brazil. That sediment volume, the researchers note, is equivalent to about two and a half Olympic swimming pools, or roughly 407 dump truckloads, moved by worms in just four days. The work, published in the journal Discover Ecology, represents one of the first attempts to scale up the ecological functions of estuarine invertebrates from laboratory bench measurements to an entire ecosystem.</p>
<p>The research team, led by Amanda Martins of the Federal University of Bahia together with Marcos Krull and Francisco Barros, combined two rarely united sources of evidence: a long-term benthic monitoring dataset stretching back to 2004, and controlled laboratory experiments that measured exactly how much organic matter individual worms eat and how much sediment they displace. The monitoring data came from ten sampling stations along the estuary&#8217;s salinity gradient, surveyed on six separate occasions between 2004 and 2022. At each station, researchers collected cores of sediment, sieved the samples through a 0.5 millimeter mesh, and identified the invertebrates to the family level. Polychaetes made up more than half of all benthic macroinvertebrates in the system, making them the natural focal group for the study.</p>
<p>To translate counts of worms into estimates of ecosystem-wide function, the team turned to Bayesian generalized linear mixed models, a statistical framework that allows researchers to predict abundance across unsampled areas while quantifying uncertainty. The models incorporated environmental predictors including salinity and sediment grain size fractions—ranging from coarse sand upstream to fine sand and mud downstream—drawn from high-resolution environmental layers covering the modeled estuarine portion of the system. The researchers tested both Poisson and negative binomial distributions, with and without zero-inflation parameters, and compared generalized additive and generalized linear mixed models. Model selection relied on leave-one-out cross-validation using Pareto-smoothed importance sampling, and the winning models were fitted with Markov Chain Monte Carlo methods using a Hamiltonian sampler, with four independent chains and weakly informative priors to regularize the estimates.</p>
<p>The result of this statistical machinery was a population estimate of roughly 2,062.5 million individual polychaetes across the estuarine system, with a 95 percent credible interval spanning about 1.87 to 2.63 billion individuals. Seven families dominated the analysis: Orbiniidae, Spionidae, Eunicidae, Pilargidae, Lumbrineridae, Onuphidae, and Goniadidae. Orbiniidae alone accounted for an estimated 1,045.9 million individuals, followed by Onuphidae with 671.6 million. Densities were highest in the marine-influenced regions of the estuary, particularly for these two dominant families, setting the stage for a strongly spatially patterned delivery of ecological functions.</p>
<p>The functional measurements themselves came from a previous experimental study in which worms collected from the Jaguaripe estuary were kept under controlled laboratory conditions. Organic matter decomposition was quantified as the consumption rate of standardized pieces of shrimp tissue over 96 hours, corrected for natural decomposition using controls. Bioturbation—the reworking of sediment—was measured as the volume of sediment displaced by each species, reconstructed from computed tomography scans of the burrow systems the worms produced. This CT-based approach allowed the researchers to visualize and measure the three-dimensional architecture of worm burrows without disturbing them, providing an unusually precise metric of a notoriously difficult-to-quantify process.</p>
<p>When the per-individual rates were multiplied by the model-predicted abundances across the estuary, the numbers were striking. Polychaetes consumed an estimated 232.56 tons of organic material over 96 hours, with Orbiniidae responsible for 123.16 tons—about 53 percent of the total—and Onuphidae contributing another 89.81 tons, or nearly 39 percent. Bioturbation totaled an estimated 6,098.3 cubic meters of sediment over the same period, again dominated by Orbiniidae at 4,495.1 cubic meters and Onuphidae at 1,070.7 cubic meters, together accounting for more than 91 percent of the total. Smaller families such as Eunicidae, Spionidae, and Lumbrineridae contributed comparatively little to bioturbation, while Eunicidae and Pilargidae were minor players in organic matter consumption as well.</p>
<p>The spatial patterns were equally revealing. Both functions peaked in regions of elevated salinity, in the euhaline and polyhaline zones near the estuary&#8217;s mouth. Orbiniidae and Onuphidae delivered their largest contributions at salinities between 25 and 40, whereas Spionidae showed a strikingly different profile, contributing up to 80 percent of decomposition and bioturbation in the lower-salinity upstream reaches, between roughly 5 and 20 on the salinity scale. Sediment grain size also mattered: the dominant families responded to different granulometric fractions, with Orbiniidae and Onuphidae key in coarse sand and mud regions respectively, and Spionidae playing its characteristic upstream role in very fine sand. No single sediment variable was consistently selected across all taxa, underscoring that each family responds to its own combination of environmental conditions.</p>
<p>Correlation analyses of the functional contributions revealed another important pattern: functional redundancy. In the marine lower estuary, the contributions of Orbiniidae, Onuphidae, and Lumbrineridae rose and fell together, with correlation coefficients for bioturbation reaching 0.93 between Orbiniidae and Onuphidae and 0.92 between Lumbrineridae and Onuphidae. This overlap means that if one family were lost, others performing similar roles could partially compensate, buffering the ecosystem against disturbance. In the oligohaline upstream zones, by contrast, fewer families contributed to the functions, and redundancy was correspondingly lower—making those reaches potentially more vulnerable to species loss. Spionidae, with low correlations to all other taxa, stands out as functionally irreplaceable in the upstream areas where it dominates.</p>
<p>The study&#8217;s authors are candid about its limitations. Only seven families and two functions were analyzed, other taxa in the estuary may contribute substantially, and variables such as food resources beyond the measured organic matter could not be included. The decomposition measurements represent early-stage, macrofauna-mediated breakdown driven by direct consumption at the sediment surface, not the full complexity of benthic metabolism. Body size, which likely influences per-individual function, could not be incorporated because weight data were unavailable for several taxa. Still, the researchers argue, the demonstration that laboratory experiments can be combined with long-term monitoring and Bayesian modeling to produce ecosystem-level estimates is itself a methodological advance, offering a template for other systems where functional data remain scarce—particularly in the tropics, where most species-specific functional measurements to date have been conducted in temperate terrestrial environments.</p>
<p>The broader implications extend to conservation and climate adaptation. Estuaries are hotspots of organic matter input and nutrient cycling, disproportionately productive relative to their area, yet they face mounting pressures from eutrophication, metal pollution, shrimp farming, and sea-level rise. Because polychaete bioturbation aerates deeper sediment layers, reduces compaction, and accelerates organic matter processing, the loss of these worms could tip sediments toward anoxia, with cascading effects on entire benthic communities. The functional maps generated by the study highlight regions of high activity that could guide conservation priorities, and the identification of low-redundancy upstream zones flags areas where monitoring should be intensified. As climate change reshapes salinity gradients and species distributions, the authors suggest that modeling the distribution and functioning of organisms under future scenarios will be essential for predicting trends—and for protecting the billions of small engineers whose invisible labor keeps coastal ecosystems running.</p>
<p><strong>Subject of Research:</strong> Ecosystem-level estimation of polychaete-mediated organic matter decomposition and bioturbation in a tropical estuary</p>
<p><strong>Article Title:</strong> Scaling up polychaete contributions to estuarine ecosystem functions</p>
<p><strong>Article References:</strong> Martins, A., Krull, M., &amp; Barros, F. (2026). Scaling up polychaete contributions to estuarine ecosystem functions. <em>Discover Ecology, 2</em>(1), Article 6. <a href="https://doi.org/10.1007/s44396-026-00023-2" rel="noopener noreferrer">https://doi.org/10.1007/s44396-026-00023-2</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44396-026-00023-2" rel="noopener noreferrer">10.1007/s44396-026-00023-2</a></p>
<p><strong>Keywords:</strong> polychaetes, estuarine ecology, bioturbation, organic matter decomposition, ecosystem functioning, Bayesian modeling, functional redundancy, salinity gradient, macrofauna, tropical estuary, sediment reworking, conservation</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">211498</post-id>	</item>
		<item>
		<title>Sacred Forests of Eastern India Prove to Be Powerful Engines of Nutrient Cycling</title>
		<link>https://scienmag.com/sacred-forests-of-eastern-india-prove-to-be-powerful-engines-of-nutrient-cycling/</link>
		
		<dc:creator><![CDATA[Chloe Pearson]]></dc:creator>
		<pubDate>Sun, 20 Sep 2026 21:45:25 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[biocultural conservation]]></category>
		<category><![CDATA[biodiversity preservation through cultural practices]]></category>
		<category><![CDATA[community-led biodiversity conservation]]></category>
		<category><![CDATA[decomposition]]></category>
		<category><![CDATA[ecological significance of sacred groves]]></category>
		<category><![CDATA[ecosystem functioning]]></category>
		<category><![CDATA[in situ conservation of biodiversity]]></category>
		<category><![CDATA[leaf litter]]></category>
		<category><![CDATA[leaf litter decomposition rates]]></category>
		<category><![CDATA[litterbags]]></category>
		<category><![CDATA[litterfall]]></category>
		<category><![CDATA[nutrient cycling]]></category>
		<category><![CDATA[nutrient cycling in tropical forests]]></category>
		<category><![CDATA[nutrient flux in sacred woodlands]]></category>
		<category><![CDATA[nutrient recycling efficiency in protected forests]]></category>
		<category><![CDATA[Odisha]]></category>
		<category><![CDATA[religious protection of forests]]></category>
		<category><![CDATA[sacred forests]]></category>
		<category><![CDATA[Sacred forests of Odisha]]></category>
		<category><![CDATA[sal-dominated forest ecosystems]]></category>
		<category><![CDATA[seasonal effects on forest floor processes]]></category>
		<category><![CDATA[Shorea robusta]]></category>
		<category><![CDATA[soil fertility]]></category>
		<category><![CDATA[tropical dry deciduous forest]]></category>
		<category><![CDATA[tropical savanna climate impact on forests]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=203216</guid>

					<description><![CDATA[A year-long study of four sacred forests in Western Odisha, India, reveals exceptionally high litterfall and rapid decomposition that make these culturally protected groves powerful engines of nutrient cycling.]]></description>
										<content:encoded><![CDATA[<p>Deep in the western districts of Odisha, India, small patches of forest have been protected for generations not by fences or legislation, but by faith. These sacred forests, guarded by local communities through religious beliefs and cultural traditions, are among the oldest forms of in situ biodiversity conservation on the subcontinent. A new year-long study has now revealed that these culturally protected woodlands are not merely spiritual refuges; they are also remarkably efficient nutrient-recycling machines, churning through leaf litter at speeds that rival or exceed those of better-studied tropical forests.</p>
<p>Researchers from Sambalpur University, Terracon Ecotech, and the Government of Odisha set out to quantify litterfall production, standing litter biomass, decomposition rates, and nutrient fluxes in four sacred forests across the region: Andhari, Dedungri, Medha, and Papanga. Three of the sites are dominated by sal (Shorea robusta), while Papanga is dominated by Cleistanthus collinus. The forests lie within a tropical savanna climate zone, where annual rainfall ranges from 900 to 1,400 millimeters, almost all of it delivered during the June-to-September monsoon, and where pre-monsoon temperatures can exceed 45 degrees Celsius. That pronounced seasonality shapes nearly everything that happens on the forest floor.</p>
<p>Between January and December 2023, the team measured litter inputs monthly using one-square-meter collection pits established at least ten meters inside each forest boundary to avoid edge effects. The collected material was separated into leaves, twigs, branches, and miscellaneous fragments, then oven-dried and weighed. Annual litterfall ranged from 8.59 megagrams per hectare per year at Andhari to 11.32 megagrams per hectare per year at Medha, figures that sit comfortably within the global range for tropical forests and actually exceed values reported for several other tropical dry deciduous forests in India. Leaves dominated the mix, contributing between 80.65 and 83.35 percent of total litterfall, followed by twigs, branches, and other material.</p>
<p>The seasonal signal was unmistakable. Litter production peaked in March at all four sites, coinciding with the height of the dry season, when water stress triggers leaf senescence and abscission in deciduous trees. Statistical analysis confirmed that month-to-month variation within sites was highly significant, while differences among the four forests were not. In other words, climate and phenology, not site identity, are the primary engines driving litterfall in these ecosystems. Standing litter biomass followed the same rhythm, accumulating to a maximum in March and dwindling to a minimum during the rainy and post-rainy months of August through November, with annual means ranging from 2.39 megagrams per hectare at Andhari to 2.68 at Medha.</p>
<p>The speed at which that litter disappeared was the study&#8217;s most striking finding. Using the classic litterbag technique, the researchers placed 20-gram samples of mixed-species fresh leaf litter, collected during the February-March peak litterfall period, into 20-by-20-centimeter nylon bags with one-millimeter mesh and laid them on the forest floor in a completely randomized design. Six bags were retrieved from each site every month. Roughly 95 percent of the initial litter mass had vanished within six months at every site. The fitted decay constants ranged from 5.75 to 6.65 per year, corresponding to half-lives of just 38 to 44 days. Model-based extrapolation suggested that 99 percent decomposition would be achieved within 274 to 318 days, although the authors caution that these figures extend beyond the six-month observation window.</p>
<p>Litter turnover rates told a similar story. The ratio of annual litterfall to standing litter biomass, a standard index of how quickly organic matter cycles through the forest floor, ranged from 3.59 to 4.22 per year, equivalent to residence times of only 87 to 102 days. Those turnover rates are higher than values reported for tropical semi-deciduous, tropical dry evergreen, and tropical evergreen forests, indicating that these small sacred groves process organic matter unusually fast. The researchers attribute the rapid decay to favorable temperature and moisture conditions during the decomposition period, which stimulate microbial activity, possibly combined with relatively high litter nutrient quality.</p>
<p>That quality question was addressed through chemical analysis of the mixed-species litter. Initial concentrations of nitrogen, phosphorus, and potassium differed significantly among the four forests, with Papanga showing the highest nutrient levels and the most favorable stoichiometric profile. Correlation analyses revealed that initial nitrogen and phosphorus concentrations were significantly associated with decomposition rates, while carbon content was not. The authors note an important caveat: lignin and cellulose, structural compounds that strongly regulate decomposability, were not measured, so the full biochemical picture of litter quality in these forests remains incomplete.</p>
<p>Nutrient release during decomposition followed a clear hierarchy: potassium was lost fastest, followed by nitrogen, then phosphorus. Potassium, highly soluble and prone to leaching, declined rapidly throughout the experiment, with release reaching 98.72 to 99.20 percent across the sites. Nitrogen loss ranged from 92.26 to 95.08 percent, and phosphorus from 80.54 to 95.34 percent after six months. Papanga recorded the highest total nutrient loss at 96.57 percent. Meanwhile, nitrogen and phosphorus concentrations actually increased in the residual litter, a pattern the researchers attribute to microbial immobilization, in which decomposer organisms accumulate these nutrients in their own biomass before releasing them back to the soil. Carbon concentrations remained relatively stable at Andhari and Medha but declined at Dedungri and Papanga.</p>
<p>The study&#8217;s authors are candid about its limitations. There were no non-sacred control forests for direct comparison, so the work characterizes variation within sacred forests rather than testing the effects of sacred-forest protection itself. Repeated temporal observations were not analyzed with mixed-effects models, and the correlation results should be read as associations rather than causal claims. Still, the baseline data fill a genuine gap: while litterfall and nutrient cycling have been extensively documented in tropical evergreen forests and, to a lesser degree, in sacred groves elsewhere in India, comparable information for the dry deciduous sacred forests of Western Odisha had been essentially absent.</p>
<p>The implications extend beyond ecology into conservation policy. Sacred forests persist as biodiversity hotspots and providers of ecosystem services, including carbon sequestration, water regulation, and soil conservation, precisely because community restrictions limit timber extraction, grazing, and fuelwood collection. Yet pressures such as fuelwood harvesting, livestock grazing, and non-timber forest product extraction persist to varying degrees, with Andhari and Dedungri showing signs of moderate degradation while Medha and Papanga remain relatively well preserved. By demonstrating that these culturally protected patches sustain high litter production, rapid decomposition, and substantial nutrient turnover, the study provides quantitative evidence that sacred forests function as localized reservoirs of soil fertility in human-dominated landscapes. As land-use intensification continues across tropical India, the researchers argue, protecting these living laboratories of biocultural conservation may be one of the most cost-effective strategies for maintaining nutrient cycling and ecological resilience in dry deciduous landscapes.</p>
<p><strong>Subject of Research:</strong> Litterfall production, decomposition rates, and nutrient cycling in tropical dry deciduous sacred forests of Western Odisha, India</p>
<p><strong>Article Title:</strong> Litterfall dynamics and decomposition-driven nutrient cycling in sacred forests of Eastern India</p>
<p><strong>Article References:</strong> Pradhan, A., Mansingh, A., Gopinath, J. S., &amp; Ekka, N. J. (2026). Litterfall dynamics and decomposition-driven nutrient cycling in sacred forests of Eastern India. <em>Discover Plants, 3</em>(1), Article 412. <a href="https://doi.org/10.1007/s44372-026-00892-7" rel="noopener noreferrer">https://doi.org/10.1007/s44372-026-00892-7</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44372-026-00892-7" rel="noopener noreferrer">10.1007/s44372-026-00892-7</a></p>
<p><strong>Keywords:</strong> litterfall, decomposition, nutrient cycling, sacred forests, tropical dry deciduous forest, Odisha, Shorea robusta, litterbags, soil fertility, ecosystem functioning, biocultural conservation, leaf litter</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">203216</post-id>	</item>
		<item>
		<title>Tree Diversity and Fungal Partners Drive Forest Life Below Ground More Than Above</title>
		<link>https://scienmag.com/tree-diversity-and-fungal-partners-drive-forest-life-below-ground-more-than-above/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 04:19:54 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[below ground ecosystem dynamics]]></category>
		<category><![CDATA[belowground ecology]]></category>
		<category><![CDATA[biodiversity]]></category>
		<category><![CDATA[ecosystem functioning]]></category>
		<category><![CDATA[Forest biodiversity]]></category>
		<category><![CDATA[forest biodiversity drivers]]></category>
		<category><![CDATA[forest ecology]]></category>
		<category><![CDATA[forest restoration]]></category>
		<category><![CDATA[fungal partnerships in forest health]]></category>
		<category><![CDATA[influence of tree composition on soil life]]></category>
		<category><![CDATA[multitrophic interactions]]></category>
		<category><![CDATA[mycorrhiza]]></category>
		<category><![CDATA[mycorrhizal fungi and tree diversity]]></category>
		<category><![CDATA[Nature Ecology & Evolution]]></category>
		<category><![CDATA[role of fungi in forest ecosystems]]></category>
		<category><![CDATA[soil food webs]]></category>
		<category><![CDATA[soil microorganisms in forests]]></category>
		<category><![CDATA[soil nutrient exchange in forests]]></category>
		<category><![CDATA[symbiosis]]></category>
		<category><![CDATA[tree diversity]]></category>
		<category><![CDATA[tree species diversity impact]]></category>
		<category><![CDATA[trophic levels]]></category>
		<category><![CDATA[underground forest ecology]]></category>
		<category><![CDATA[underground interactions in forests]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=193710</guid>

					<description><![CDATA[A large-scale forest experiment reveals that tree species richness and mycorrhizal fungal dominance independently shape biodiversity across food webs, with the strongest effects occurring below ground.]]></description>
										<content:encoded><![CDATA[<p>Forests are often celebrated for what we can see — the towering trunks, layered canopies, and the birds and insects that move through them. Yet a new study published in Nature Ecology &amp; Evolution suggests that much of the real action in a forest ecosystem happens underground, where an intricate web of roots, fungi, and soil organisms responds to the composition of the trees above in ways that scientists are only beginning to untangle. The research, based on a large-scale experiment combining tree diversity with mycorrhizal fungal dominance, provides some of the clearest evidence yet that two fundamental features of forest stands — how many tree species grow together and which types of root-associated fungi dominate — independently shape biodiversity across multiple trophic levels.</p>
<p>The study addresses a long-standing puzzle in forest ecology. For decades, researchers have documented that forests with more tree species tend to support more diverse communities of animals, fungi, and microorganisms, a pattern broadly consistent with the idea that greater plant diversity creates more niches, more resources, and more structural complexity. At the same time, ecologists have recognized that nearly all tree species form symbiotic relationships with mycorrhizal fungi — root-dwelling partners that exchange soil nutrients for plant carbon — and that the two dominant types of these symbioses, associated with different nutrient-acquisition strategies, create profoundly different soil environments. What has remained unclear is whether these two factors operate independently, interact with one another, or merely reflect the same underlying gradient of forest conditions.</p>
<p>Disentangling these effects requires a special kind of experiment, one in which tree diversity and mycorrhizal composition are manipulated deliberately rather than merely observed. The researchers behind the new study designed exactly such an experiment, establishing forest plots in which the number of tree species and the identity of the mycorrhizal types associated with those trees were controlled in a replicated design. This approach allowed the team to statistically separate the influence of tree species richness from the influence of mycorrhizal dominance, and to measure how each factor cascades through food webs both above the soil surface and within it.</p>
<p>The central finding is striking: tree diversity and mycorrhizal type each exert their own distinct influence on the diversity of organisms at higher trophic levels, and these influences do not simply collapse into a single combined effect. In other words, a forest&#8217;s capacity to support diverse communities of herbivores, predators, decomposers, and microbes depends both on how many tree species are present and on which fungal symbionts dominate the root systems — and knowing one of these factors does not allow scientists to predict the other. This independence has important implications, because it means that conservation and restoration strategies targeting only one of these dimensions may miss critical levers for supporting biodiversity.</p>
<p>Perhaps the most consequential result concerns the direction of these effects relative to the soil surface. While tree diversity and mycorrhizal composition shaped communities both above and below ground, the strength of their influence was consistently greater below ground. Organisms living in the soil — from fungal and bacterial decomposers to root-feeding insects and the predators that hunt them — responded more strongly to variation in tree diversity and mycorrhizal type than did organisms living in the canopy and on the forest floor above. This asymmetry makes intuitive sense once the biology is considered: soil communities are physically close to the roots and fungal networks through which trees channel carbon and draw up nutrients, so any change in the composition of those roots and symbionts propagates rapidly through the belowground food web.</p>
<p>The belowground emphasis of the findings adds to a growing appreciation among ecologists that soils are not merely a substrate supporting plant life but a vast reservoir of biodiversity in their own right. A single handful of forest soil can contain thousands of species of bacteria, fungi, and microscopic animals, many of which remain formally undescribed. These organisms drive the decomposition of organic matter, the cycling of nitrogen and phosphorus, and the formation of soil structure — processes on which forest productivity and, ultimately, the global carbon cycle depend. If the diversity and composition of these communities are governed largely by the trees and their fungal partners above them, then the way forests are planted, managed, and restored will echo through soil ecosystems for decades.</p>
<p>The mycorrhizal dimension of the study deserves particular attention. Trees are commonly categorized by the type of mycorrhizal association they form, with two major groups dominating temperate and boreal forests. One group of fungi is especially adept at accessing nitrogen directly from organic matter in the soil, while the other excels at scavenging inorganic nutrients over larger soil volumes. These different strategies leave different chemical fingerprints on the soil: stands dominated by one mycorrhizal type tend to accumulate organic layers and cycle nutrients more slowly, while stands dominated by the other foster faster decomposition and different microbial assemblages. By manipulating which type dominated their experimental plots, the researchers could show that these fungal legacies shape entire communities of soil organisms independently of how many tree species were planted.</p>
<p>The experimental design also allowed the team to examine how the two factors play out across trophic levels — the successive tiers of a food web, from primary producers through herbivores and decomposers to predators. The results indicate that the influence of tree diversity and mycorrhizal type propagates upward and outward through these levels, affecting not only the organisms that directly consume plant material or live on roots, but also the predators and higher-order consumers that depend on them. This multitrophic perspective is critical for understanding ecosystem functioning, because the diversity of consumers influences processes such as herbivore control, pollination, and the rate at which organic matter is broken down and its nutrients returned to the soil.</p>
<p>For forest managers and policymakers, the findings arrive at a moment when tree planting and forest restoration have become central pillars of climate and biodiversity policy around the world. Ambitious pledges to plant billions of trees frequently emphasize quantity — how many trees, how many hectares — while giving far less attention to which species are planted and in what combinations. The new study suggests that such considerations are not ecological fine print but fundamental determinants of how much biodiversity a restored forest can support. Mixtures of tree species spanning different mycorrhizal types, the results imply, are likely to support richer and more functionally robust communities both above and below ground than monocultures or narrowly composed plantations.</p>
<p>The research also carries implications for how scientists model and predict the consequences of global environmental change. As climate shifts, air pollution alters nutrient deposition, and land-use change simplifies forests, both tree diversity and the relative abundance of different mycorrhizal types are expected to change — often in ways that reinforce one another. Understanding that these two drivers operate independently gives modelers a clearer framework for predicting how forest biodiversity will respond, and it highlights the belowground realm as the arena where those responses will be felt most strongly and most rapidly. It is a reminder that the invisible architecture of roots and fungi beneath a forest floor may be as important to the future of biodiversity as the visible trees rising above it.</p>
<p>Beyond their immediate findings, studies of this kind contribute to a broader methodological shift in ecology. Observational surveys, while valuable, often struggle to separate correlated variables, because in natural forests tree species richness and mycorrhizal composition frequently co-vary with soil age, moisture, and land-use history. Manipulative experiments such as the one underlying this research allow ecologists to assign plots to combinations of tree species and mycorrhizal types at random, so that differences in biodiversity among plots can be attributed with confidence to the manipulated factors rather than to confounding environmental gradients. This is the same logic that underpins long-running grassland biodiversity experiments, which helped establish the relationship between plant diversity and ecosystem productivity decades ago, now extended to forest systems where trees interact with symbiotic fungi over much longer timescales.</p>
<p>The distinction between the two major mycorrhizal types also connects to fundamental biogeochemistry. Because one type mobilizes nitrogen from organic residues while the other relies more heavily on inorganic uptake, the two associations are associated with different rates of carbon storage in soils and different patterns of nutrient loss through leaching. Communities of decomposer animals, bacteria, and protists assemble differently under these contrasting conditions, which helps explain why belowground food webs responded so strongly in the experiment. For restoration practice, the practical takeaway is that species selection lists for planting programs could usefully include mycorrhizal type alongside growth rate and climate suitability, ensuring that new forests recreate not only the visible structure of natural stands but also the subterranean partnerships that sustain their biodiversity.</p>
<p><strong>Subject of Research:</strong> The independent effects of tree diversity and mycorrhizal fungal type on above- and belowground multitrophic biodiversity in forests.</p>
<p><strong>Article Title:</strong> Tree diversity and mycorrhizal type independently shape multitrophic biodiversity, with stronger effects belowground than aboveground</p>
<p><strong>Article References:</strong> Yi, H., Ferlian, O., Becker, P. J., Christel, H., Huang, Y., Köhler, M., Meier, I. C., Ul Haq, H., Wubet, T., &amp; Eisenhauer, N. (2026). Tree diversity and mycorrhizal type independently shape multitrophic biodiversity, with stronger effects belowground than aboveground. <em>Nature Ecology &amp;amp; Evolution, 10</em>(9), 1628-1643. <a href="https://doi.org/10.1038/s41559-026-03147-6" rel="noopener noreferrer">https://doi.org/10.1038/s41559-026-03147-6</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1038/s41559-026-03147-6" rel="noopener noreferrer">10.1038/s41559-026-03147-6</a></p>
<p><strong>Keywords:</strong> tree diversity, mycorrhiza, forest ecology, biodiversity, soil food webs, belowground ecology, ecosystem functioning, symbiosis, trophic levels, forest restoration, Nature Ecology &amp; Evolution, multitrophic interactions</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">193710</post-id>	</item>
	</channel>
</rss>
