<?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>ammonium nitrogen &#8211; Science</title>
	<atom:link href="https://scienmag.com/tag/ammonium-nitrogen/feed/" rel="self" type="application/rss+xml" />
	<link>https://scienmag.com</link>
	<description></description>
	<lastBuildDate>Sun, 04 Oct 2026 04:24:06 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.1.3</generator>

<image>
	<url>https://scienmag.com/wp-content/uploads/2024/07/cropped-scienmag_ico-32x32.jpg</url>
	<title>ammonium nitrogen &#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>Tiny Soil Worms Rewrite the Rules of Life on Arid Mountains</title>
		<link>https://scienmag.com/tiny-soil-worms-rewrite-the-rules-of-life-on-arid-mountains/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Sun, 04 Oct 2026 04:24:06 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[adaptation of soil worms to drought]]></category>
		<category><![CDATA[ammonium nitrogen]]></category>
		<category><![CDATA[arid mountain ecosystems]]></category>
		<category><![CDATA[biodiversity]]></category>
		<category><![CDATA[community assembly]]></category>
		<category><![CDATA[dispersal and chance in soil organism communities]]></category>
		<category><![CDATA[drought adaptation]]></category>
		<category><![CDATA[drought resilience in soil organisms]]></category>
		<category><![CDATA[dry-hot valley]]></category>
		<category><![CDATA[ecological role of nematodes in fragile environments]]></category>
		<category><![CDATA[ecology of dry-hot valleys]]></category>
		<category><![CDATA[elevation effects on soil biodiversity]]></category>
		<category><![CDATA[elevation gradient]]></category>
		<category><![CDATA[impact of Foehn effect on soil communities]]></category>
		<category><![CDATA[microbial and microscopic soil fauna]]></category>
		<category><![CDATA[microbial biomass carbon]]></category>
		<category><![CDATA[nutrient availability in dry soils]]></category>
		<category><![CDATA[soil food web]]></category>
		<category><![CDATA[soil moisture]]></category>
		<category><![CDATA[soil nematodes]]></category>
		<category><![CDATA[soil nutrients]]></category>
		<category><![CDATA[Yunnan China]]></category>
		<category><![CDATA[Yunnan Province dry-hot valley ecology]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=233478</guid>

					<description><![CDATA[A study in China's Yuanjiang Dry-Hot Valley finds that soil nematode abundance rises with elevation and moisture, while nutrient chemistry and dispersal limitation, not drought filtering, drive the assembly of these hidden soil communities.]]></description>
										<content:encoded><![CDATA[<p>Deep beneath the scorched savannas of southwestern China, an unassuming cast of microscopic worms is challenging one of ecology&#8217;s most stubborn assumptions. Soil nematodes, threadlike animals barely visible to the naked eye, have long been treated as prisoners of water: where soils dry out, these creatures are expected to dwindle, and where moisture returns, they are expected to rebound. A new study conducted in the Yuanjiang Dry-Hot Valley of Yunnan Province confirms half of that expectation and upends the other half, revealing that communities of these worms are shaped not simply by drought, but by a subtle interplay of nutrients, dispersal, and chance that shifts dramatically with elevation.</p>
<p>The research, published in the journal Ecology and Evolution, focused on one of the most ecologically fragile landscapes in Asia. The Yuanjiang Dry-Hot Valley is an anomaly born of physics: subsiding air currents and the Foehn effect, in which air descends and warms as it spills over mountains, combine to create a parched, savanna-like climate in the heart of otherwise humid southwestern China. At the valley floor, soils hold little water and plants such as Heteropogon contortus, Euphorbia royleana, and Woodfordia fruticosa dominate the landscape. Climb toward 1600 meters, however, and the vegetation transitions into relatively intact montane evergreen broadleaf forest, with both precipitation and soil moisture rising steadily with altitude. That steep environmental gradient, compressed into a single mountainside, makes the valley a natural laboratory for asking how belowground life responds to drought.</p>
<p>Why should anyone care about worms too small to see? The answer lies in their ecological leverage. Nematodes occupy multiple trophic levels in the soil: bacterivores graze on bacteria, fungivores consume fungi, plant parasites feed on roots, and omnivore-predators sit near the top of the soil food web. Because they thread through so many links in the underground economy, nematodes help regulate carbon and nitrogen cycling, processes with consequences that ripple all the way to the atmosphere. Yet despite their importance, belowground biodiversity along elevational gradients remains strikingly understudied, particularly in arid and semi-arid mountains, where most ecological attention has historically gone to the more visible life above ground.</p>
<p>The research team, working from the Yuanjiang Dry-Hot Valley Ecological Station, sampled soils at four elevations: 400, 800, 1200, and 1600 meters. In October 2023 and January 2024, they established plots in flat terrain, collected soil from the top ten centimeters, and extracted live nematodes using the classic Baermann funnel technique, in which active worms migrate through water over 48 hours. Under a Leica microscope, the researchers identified nematodes to genus based on morphological characteristics and sorted them into the four feeding groups. In parallel, they measured a battery of soil properties: moisture, pH, ammonium and nitrate nitrogen, available and total phosphorus, total nitrogen, soil organic carbon, dissolved organic carbon, and microbial biomass carbon.</p>
<p>The first headline result was deceptively simple: total nematode abundance and diversity were lowest at 400 meters and rose significantly with elevation. All four feeding groups had their lowest abundances at the valley floor, and the pattern tracked soil moisture, which climbed from a mere 6.34 percent at 400 meters. This makes intuitive sense. Nematodes live in the thin water films that coat soil particles and depend on those films to move, feed, and reproduce. In a drought-stricken valley floor, the aquatic highways of the soil effectively vanish. But the story quickly grew more complicated. Bacterivore and omnivore-predator abundances were also shaped by soil pH and available phosphorus, while fungivore abundance correlated negatively with microbial biomass carbon and dissolved organic carbon. Moisture, in other words, was only part of the equation.</p>
<p>Nutrients turned out to play a surprisingly dual role. Ammonium nitrogen, which increased with elevation, boosted both the abundance and diversity of plant-parasitic nematodes, likely because nitrogen enrichment enhances the plant resources those parasites exploit. Yet the same compound reduced the diversity of bacterivores and fungivores, apparently acting as a toxic selective pressure on these environmentally sensitive groups. Ammonium thus functions simultaneously as a resource and a filter, promoting some lineages while pruning others. Meanwhile, microbial biomass carbon, a proxy for the food available to microbe-eating nematodes, increased bacterivore diversity, and available phosphorus raised the abundances of bacterivores and plant parasites. When the researchers ranked the drivers of overall community composition, microbial biomass carbon and ammonium nitrogen outperformed soil moisture itself, explaining 62.5 percent and 59.3 percent of the variation respectively.</p>
<p>The study&#8217;s most provocative findings came from community assembly theory, which asks whether ecological communities are built by predictable forces or by luck. Deterministic processes, such as environmental filtering and competition, produce communities that track environmental gradients in a repeatable way. Stochastic processes, including random birth, death, and dispersal events, produce communities that are largely unpredictable. The researchers applied a neutral community model, in which a goodness-of-fit value close to one indicates that randomness fully explains community structure. Conventional wisdom, and the team&#8217;s own hypothesis, held that drought acts as a harsh environmental filter, making assembly more deterministic at the hot, dry valley floor and more random as conditions ease uphill.</p>
<p>The data said otherwise. The share of community variation explained by stochastic processes actually declined with elevation, falling from 53.2 percent at 400 meters to 34.9 percent at 1600 meters. Rather than being filtered out by drought, the valley&#8217;s nematodes appear to have adapted to it. The dominant genus at low elevations, Acrobeles, is typically drought-tolerant, suggesting that these communities have evolved to withstand the very conditions once assumed to exclude them. At the valley floor, low moisture suppresses nematode abundance and limits dispersal, and dispersal limitation is a well-known amplifier of randomness in community assembly. Meanwhile, the higher concentrations of microbial biomass carbon and available phosphorus, and lower ammonium levels, at low elevations eased environmental stress, further weakening deterministic filtering. In arid systems, moisture seems to govern nematode communities indirectly, by controlling how many worms exist and how far they travel, rather than by directly screening species.</p>
<p>These findings carry implications well beyond one Chinese valley. As climate models project more frequent and intense droughts across the globe, understanding how soil fauna persist under water stress becomes a matter of predicting how nutrient cycling itself will respond. If drought-adapted nematode communities can persist at the dry end of a gradient, belowground food webs may prove more resilient than feared, but the study also shows that nutrient shifts, particularly nitrogen enrichment, can restructure these communities in ways that moisture alone cannot explain. The dual action of ammonium, feeding plant parasites while suppressing microbial grazers, hints that atmospheric nitrogen deposition could quietly reshape soil food webs even where water is plentiful.</p>
<p>There is also a methodological lesson. Elevational studies of soil biodiversity have reported declining, increasing, and mid-elevation peak patterns in different systems, a confusing spread of results that this study helps untangle by separating abundance from diversity and both from community composition. In the Yuanjiang Dry-Hot Valley, abundance rose with moisture, diversity responded to nutrient chemistry, and assembly stochasticity followed dispersal dynamics. Three different ecological currencies, three different rules. For a field that has long treated the soil as a black box beneath more charismatic mountaintop biodiversity, the message from these microscopic worms is clear: the underground story of climate change is being written in water, nutrients, and chance all at once, and only by reading all three can ecologists predict how the hidden majority of terrestrial life will fare as the world&#8217;s drylands expand.</p>
<p><strong>Subject of Research:</strong> Elevational distribution and community assembly mechanisms of soil nematodes in an arid dry-hot valley ecosystem</p>
<p><strong>Article Title:</strong> Distribution Patterns and Community Assembly of Soil Nematodes Along Elevation Gradients in a Dry‐Hot Valley</p>
<p><strong>Article References:</strong> Zhang, J., Lei, H., Lin, N., Hou, C., Yue, C., Chen, Y., &amp; Wu, J. (2026). Distribution Patterns and Community Assembly of Soil Nematodes Along Elevation Gradients in a Dry‐Hot Valley. <em>Ecology and Evolution, 16</em>(10), Article e74358. <a href="https://doi.org/10.1002/ece3.74358" rel="noopener noreferrer">https://doi.org/10.1002/ece3.74358</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1002/ece3.74358" rel="noopener noreferrer">10.1002/ece3.74358</a></p>
<p><strong>Keywords:</strong> soil nematodes, elevation gradient, dry-hot valley, community assembly, soil moisture, soil nutrients, ammonium nitrogen, microbial biomass carbon, drought adaptation, biodiversity, soil food web, Yunnan China</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">233478</post-id>	</item>
		<item>
		<title>Wild Soybean Recruits Hidden Soil Microbes to Beat Saline-Alkali Stress</title>
		<link>https://scienmag.com/wild-soybean-recruits-hidden-soil-microbes-to-beat-saline-alkali-stress/</link>
		
		<dc:creator><![CDATA[Alan Morgan]]></dc:creator>
		<pubDate>Thu, 01 Oct 2026 22:51:40 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[alkaline phosphatase]]></category>
		<category><![CDATA[ammonium nitrogen]]></category>
		<category><![CDATA[crop resilience under salinity]]></category>
		<category><![CDATA[Glycine soja]]></category>
		<category><![CDATA[leucine aminopeptidase]]></category>
		<category><![CDATA[microbial community function]]></category>
		<category><![CDATA[microbial community structure]]></category>
		<category><![CDATA[microbial recruitment mechanisms]]></category>
		<category><![CDATA[plant genetics and microbiome]]></category>
		<category><![CDATA[plant stress tolerance]]></category>
		<category><![CDATA[plant-microbe interactions]]></category>
		<category><![CDATA[rhizosphere bacteria]]></category>
		<category><![CDATA[rhizosphere microbiome]]></category>
		<category><![CDATA[saline-alkali stress]]></category>
		<category><![CDATA[saline-alkali stress tolerance]]></category>
		<category><![CDATA[soil alkalinity adaptation]]></category>
		<category><![CDATA[soil bacteria]]></category>
		<category><![CDATA[soil enzymes]]></category>
		<category><![CDATA[soil functionality]]></category>
		<category><![CDATA[soil microbes]]></category>
		<category><![CDATA[soil microbial diversity]]></category>
		<category><![CDATA[stress-resistant soybean varieties]]></category>
		<category><![CDATA[wild soybean]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=224090</guid>

					<description><![CDATA[New research shows that salt-tolerant wild soybean genotypes reshape their rhizosphere bacterial communities and boost soil enzyme functionality to withstand saline-alkali stress.]]></description>
										<content:encoded><![CDATA[<p>Soil salinity and alkalinity are among the most punishing forces in agriculture, stunting crops across millions of hectares worldwide. But new research on wild soybean suggests that the secret to surviving these hostile soils may lie not only in the plant&#8217;s own genes, but in the invisible community of bacteria clustered around its roots. A study published in Plant and Soil examined how saline-alkali stress reshapes the diversity and functionality of soil microbes in wild soybean (Glycine soja), the hardy ancestor of cultivated soybean, and the findings point to a fascinating division of labor between tolerant and sensitive plant types.</p>
<p>The research team, led by Mingjing Li of Jilin Agricultural University together with colleagues at the Heilongjiang Academy of Agricultural Sciences, set out to address a gap that has frustrated both ecologists and crop breeders. It is well established that rhizosphere bacteria, the microbial community hugging the root surface and the thin layer of soil it influences, play important roles in helping plants cope with environmental stress. What has remained poorly understood, however, is how the regulatory interplay between the plant and its microbiome differs between genotypes that tolerate saline-alkali conditions and those that succumb to them.</p>
<p>To probe this question, the researchers compared three wild soybean genotypes: two designated as saline-alkali tolerant, labeled 100 and 142, and one saline-alkali sensitive type, labeled 047. By growing these types under control conditions and under saline-alkali treatment, and then analyzing the bacterial communities in the surrounding soil alongside measurements of soil chemistry and enzyme activity, the team could trace how each genotype&#8217;s microbial partnership shifted as stress mounted. The approach allowed them to connect changes in microbial community structure with tangible shifts in soil functionality.</p>
<p>One of the first signals emerged from soil nitrogen chemistry. The tolerant types, 142 and 100, maintained significantly higher contents of ammonium nitrogen (NH4+) in their rhizosphere soil than the sensitive type 047. Ammonium is a preferred nitrogen source for many plants and microbes, and its elevated presence in the tolerant genotypes hints at enhanced nitrogen cycling in the soil surrounding their roots. Because nitrogen availability is tightly coupled to microbial activity, this difference suggests that tolerant wild soybeans may cultivate a soil environment that better sustains nutrient supply even when salt and alkali pressures would otherwise suppress it.</p>
<p>Intriguingly, the overall alpha diversity of bacteria, a measure of how many different bacterial types are present within a sample, did not differ dramatically between the sensitive and tolerant soybean types. In other words, the tolerant plants were not simply hosting more diverse microbial communities. The critical distinction lay instead in the structure of the community, meaning which specific bacterial groups dominated the rhizosphere. This finding challenges the intuitive assumption that diversity alone equals resilience, and instead highlights community composition, the identity of the players, as the decisive variable.</p>
<p>At the phylum level, the tolerant genotypes showed enrichment of Pseudomonadota, Bacteroidota, and Dependentiae, while Chloroflexota was less abundant compared with the sensitive type. These shifts are meaningful because different bacterial phyla carry different metabolic repertoires. Pseudomonadota, for example, includes many species known for rapid growth, nutrient cycling, and plant growth-promoting traits. The enrichment of such groups around tolerant roots suggests the tolerant plants may actively favor microbes that contribute to stress alleviation and nutrient mobilization.</p>
<p>Drilling down to the genus level revealed even finer patterns. Under normal, unstressed conditions, the genus Pseudomonas was enriched in the sensitive genotype 047, while an unclassified member of the family Vermiphilaceae was enriched in tolerant genotype 142. When saline-alkali stress was applied, the picture shifted again: norank_f_Saprospiraceae and norank_f_Vermiphilaceae became enriched in the tolerant genotype 142, whereas Aggregatilinea and norank_f_Anaerolineaceae were less abundant in tolerant genotypes compared with the sensitive one. These microbial signatures, some rising and others falling in tandem with stress, provide a detailed fingerprint of how the rhizosphere community reorganizes around roots that are coping versus roots that are struggling.</p>
<p>The study also identified the soil factors most tightly linked to these community shifts. Soil ammonium nitrogen, alkaline phosphatase activity (AP), and L-leucine aminopeptidase activity (S-LAP) emerged as important variables associated with changes in microbial community structure. Both enzymes are workhorses of soil nutrient cycling: alkaline phosphatase liberates phosphate from organic compounds, while leucine aminopeptidase breaks down proteins into amino acids that plants and microbes can absorb. Their prominence in explaining community variation ties the microbial reorganization directly to soil nutrient dynamics, painting a coherent picture of a feedback loop between plant stress tolerance, enzyme activity, and bacterial composition.</p>
<p>Perhaps most striking was the evidence on soil functionality. Under control conditions, soil functionality was significantly higher in tolerant type 100 than in sensitive type 047. Under saline-alkali treatment, both tolerant types, 100 and 142, showed elevated functionality relative to the sensitive type. Soil functionality, which integrates the capacity of the soil to support nutrient cycling, enzyme-mediated transformations, and biological activity, is widely regarded as a cornerstone of ecosystem health. The observation that tolerant wild soybeans sustain or even boost this functionality under stress suggests that the plant-microbe partnership is not a passive byproduct of salinity but an active component of tolerance itself.</p>
<p>Taken together, the authors conclude that soil functionality can be explained by changes in bacterial community structure, and that wild soybeans may actively reshape their soil microbial communities and their functionality as a strategy to resist saline-alkali stress. The implications ripple outward in several directions. For breeders, the microbial signatures enriched in tolerant genotypes could serve as markers for selecting resilient lines, or as clues for designing synthetic microbial communities that boost salt tolerance in cultivated soybean, a crop of enormous global importance for food and feed. For soil scientists, the identification of ammonium nitrogen and specific extracellular enzymes as key mediators reinforces a growing recognition in the field that microbial community composition, rather than diversity metrics alone, underpins ecosystem multifunctionality. And for anyone worried about the spread of saline-alkali soils, the message is quietly hopeful: the genetic resources of wild relatives like Glycine soja, paired with the microbes they recruit, may hold the keys to keeping farmland productive as soils grow saltier. As the authors&#8217; results show, the roots of resilience may be planted long before the first salt crystal hits the leaf.</p>
<p><strong>Subject of Research:</strong> The response of rhizosphere soil microbial diversity and functionality to saline-alkali stress in wild soybean</p>
<p><strong>Article Title:</strong> Response of soil microbial diversity and functionality to saline-alkali in wild soybean (Glycine soja)</p>
<p><strong>Article References:</strong> Li, M., Wang, S., Sun, S., Liu, M., Fan, C., Liang, W., Ji, X., &amp; Liu, J. (2026). Response of soil microbial diversity and functionality to saline-alkali in wild soybean (Glycine soja). <em>Plant and Soil</em>. <a href="https://doi.org/10.1007/s11104-026-09090-6" rel="noopener noreferrer">https://doi.org/10.1007/s11104-026-09090-6</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s11104-026-09090-6" rel="noopener noreferrer">10.1007/s11104-026-09090-6</a></p>
<p><strong>Keywords:</strong> wild soybean, Glycine soja, saline-alkali stress, rhizosphere microbiome, soil bacteria, microbial community structure, soil enzymes, alkaline phosphatase, leucine aminopeptidase, ammonium nitrogen, soil functionality, plant stress tolerance</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">224090</post-id>	</item>
	</channel>
</rss>
