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	<title>dissolved organic carbon &#8211; Science</title>
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	<title>dissolved organic carbon &#8211; Science</title>
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		<title>Enzyme Pretreatment Shows Opposite Effects on Soil Solidification and Slurry Dewatering</title>
		<link>https://scienmag.com/enzyme-pretreatment-shows-opposite-effects-on-soil-solidification-and-slurry-dewatering/</link>
		
		<dc:creator><![CDATA[Denise Maddox]]></dc:creator>
		<pubDate>Mon, 19 Oct 2026 08:38:39 +0000</pubDate>
				<category><![CDATA[Science News]]></category>
		<category><![CDATA[Technology and Engineering]]></category>
		<category><![CDATA[ABTS]]></category>
		<category><![CDATA[binder-soil interface modification]]></category>
		<category><![CDATA[biogeotechnics]]></category>
		<category><![CDATA[calcium carbide residue]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[effects of enzymes on soil properties]]></category>
		<category><![CDATA[enzymatic pretreatment]]></category>
		<category><![CDATA[enzyme pretreatment]]></category>
		<category><![CDATA[geotechnical engineering innovations]]></category>
		<category><![CDATA[geotextile tube]]></category>
		<category><![CDATA[humic substances interference]]></category>
		<category><![CDATA[humic-rich soil]]></category>
		<category><![CDATA[laccase]]></category>
		<category><![CDATA[organic interference in soil treatment]]></category>
		<category><![CDATA[organic matter in excavation]]></category>
		<category><![CDATA[redox mediator]]></category>
		<category><![CDATA[slurry dewatering]]></category>
		<category><![CDATA[soil solidification]]></category>
		<category><![CDATA[soil solidification challenges]]></category>
		<category><![CDATA[soil stabilization]]></category>
		<category><![CDATA[sustainable soil stabilization methods]]></category>
		<category><![CDATA[unconfined compressive strength]]></category>
		<category><![CDATA[underground construction dewatering techniques]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=310974</guid>

					<description><![CDATA[Laccase enzyme pretreatment dramatically strengthens humic-rich soil for solidification but adding the ABTS mediator improves slurry dewatering instead, revealing that enzyme-mediator formulations must be tailored to the intended engineering process.]]></description>
										<content:encoded><![CDATA[<p>Excavation, tunnelling, dredging, and underground construction generate enormous volumes of fine-grained soil and high-water-content slurry that must be dewatered, stabilized, or both before transport, reuse, and disposal. When the excavated material is rich in humic substances, the central difficulty is not simply low intrinsic strength or excess water, but persistent organic interference at reactive interfaces. Carboxyl, phenolic, and other oxygen-containing groups in humic matter adsorb on mineral and binder surfaces, complex calcium- and aluminum-bearing species, retain water, and alter particle associations. In compacted binder-treated soils, these effects restrict particle-binder contact, suppress hydration-product development, and weaken the continuity of the load-bearing cemented network. Increasing cementitious reagent dosage can partly compensate for this inhibition, but it does not remove the interfacial cause of the problem, which is why researchers have been searching for ways to modify the humic-rich interface before binder addition or coagulation rather than relying solely on higher reagent dosages.</p>
<p>A new study published in Frontiers in Bioengineering and Biotechnology by Xuanyu Chen, Prithvendra Singh, Kaiwei Luo, Qianwei Ma, and Ningjun Jiang of Southeast University&#8217;s Institute of Geotechnical Engineering, working with the Jiangsu Key Laboratory of Low Carbon and Sustainable Geotechnical Engineering and the Indian Institute of Technology Bombay, has now demonstrated that laccase-based enzymatic pretreatment produces strikingly different engineering responses depending on whether the humic-rich soil is being solidified or dewatered. The research team used an artificial humic-rich soil containing 10 percent humic acid, classified as organic clay under the Unified Soil Classification System, to compare laccase pretreatment in composite-binder solidification and slurry dewatering. The artificial soil was prepared from 18 percent quartz-rich silt, 27 percent kaolin, 45 percent calcium bentonite, and 10 percent commercial humic acid, providing a reproducible humic-rich model system for comparing the tested treatment routes.</p>
<p>Laccase is well suited to modifying organic interfaces because it oxidizes a broad range of phenolic and aromatic substrates under mild aqueous conditions using molecular oxygen as the terminal electron acceptor. Its effective reaction domain can be extended with a low-molecular-mass redox mediator such as 2,2&#8242;-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), commonly abbreviated ABTS, which transfers oxidative equivalents from the enzyme to less accessible substrates. For humic-rich soil, however, a larger reaction domain cannot be assumed to be universally beneficial. Humic substances themselves participate in laccase-driven transformations and can also aggregate with or inhibit laccase, so enzyme performance depends on the physicochemical environment in which the catalytic system operates. The engineering question is therefore not whether ABTS increases laccase reactivity in isolation, but whether the resulting spatial pattern of organic transformation is favorable for the subsequent engineering process.</p>
<p>The experimental program comprised four parts: a laccase-dose comparison for solidification, a component-comparison test of laccase alone, laccase plus ABTS, and laccase plus ABTS plus carboxymethyl chitosan, bench-scale coagulation and flocculation with vacuum filtration, and geotextile-tube dewatering. For solidification, the treated soil was mixed with 8 percent of a self-developed calcium-rich composite curing agent consisting of carbide residue, gypsum, and Portland cement at a dry-mass ratio of 20:1:1 after 24 hours of pretreatment. For dewatering, the same solids were dispersed as a high-water-content slurry with an initial water content of 383.9 percent on a dry-mass basis and conditioned with polyaluminum chloride followed by carboxymethyl chitosan or cationic polyacrylamide.</p>
<p>The solidification results were unambiguous. At laccase dosages of 20,000 and 40,000 units per kilogram of dry soil, the 14-day unconfined compressive strength reached 841.4 and 818.3 kilopascals respectively, compared with only 434.9 kilopascals for the untreated control. The 20,000-unit dosage was therefore selected for subsequent experiments because increasing the nominal laccase input to 40,000 units per kilogram did not provide additional strength improvement. In the component-comparison test, the 14-day strength was 797.4 kilopascals with laccase alone, 630.6 kilopascals with laccase plus ABTS, 518.0 kilopascals with laccase plus ABTS plus carboxymethyl chitosan, and 410.6 kilopascals for the control. Laccase alone combined the highest 14-day strength with the lowest axial expansion of 1.74 percent, compared with 2.58 percent for the control. The addition of ABTS, and particularly the subsequent incorporation of carboxymethyl chitosan, progressively diminished the strengthening effect rather than providing an additive benefit.</p>
<p>Microstructural evidence from the solidification branch supported this interpretation. Scanning electron microscopy showed that the 14-day laccase-treated specimen had the densest interparticle morphology, with particle surfaces more extensively covered by cementitious products and adjacent particles connected by more continuous solid bridges. Energy-dispersive X-ray spectroscopy revealed that the calcium content increased from 9.63 weight percent in the control to 13.65 weight percent in the laccase-treated specimen, with the atomic calcium-to-silicon ratio rising from 0.410 to 0.774. X-ray diffraction patterns showed broadly similar crystalline-phase assemblages dominated by quartz, calcite, and portlandite, indicating that enzymatic pretreatment did not alter the principal aluminosilicate mineral framework but instead produced treatment-dependent differences in the relative prominence of existing calcium-bearing reflections.</p>
<p>In contrast, mediator addition benefited slurry treatment. In the bench-scale tests, laccase plus ABTS followed by polyaluminum chloride and carboxymethyl chitosan reduced supernatant turbidity to 3.73 nephelometric turbidity units, the lowest value among the chitosan-based formulations, and reduced vacuum-filtrate turbidity to 81.7 units while decreasing cake water content to 57.66 percent. Notably, two formulations with similar zeta potentials of approximately -7 millivolts showed markedly different turbidity and cake water content, indicating that charge reduction alone did not determine clarification performance. Once electrostatic repulsion is reduced, aggregate architecture, floc strength, compressibility, and pore connectivity become increasingly important in controlling dewaterability.</p>
<p>The difference between formulations became even more pronounced during geotextile-tube drainage. Although polyaluminum chloride plus cationic polyacrylamide produced the fastest initial release of water, releasing 725 milliliters within the first 5 minutes, the laccase plus ABTS plus polyaluminum chloride plus carboxymethyl chitosan route subsequently achieved the greatest cumulative water release. At 30 hours, the cumulative filtrate volume reached 1,702.8 milliliters for the enzymatic route, compared with 1,340 milliliters for polyaluminum chloride plus carboxymethyl chitosan and 1,392 milliliters for polyaluminum chloride plus cationic polyacrylamide, representing increases of 27.1 percent and 22.3 percent respectively. The final central-region cake water content was 84.94 percent for the enzymatic route, substantially lower than 112.19 percent for the chitosan route and 127.23 percent for the polyacrylamide route. The directly collected filtrate from the enzymatic route also remained relatively clear at 9.99 turbidity units, compared with 82.86 units for the chitosan route without biochemical pretreatment.</p>
<p>Dissolved organic carbon analysis revealed a paradoxical finding. The DOC concentration decreased from 40.50 milligrams of carbon per liter in untreated soil to 29.07 after laccase treatment, a reduction of 28.2 percent, and further decreased to 20.33 milligrams of carbon per liter after ABTS addition, representing a reduction of 49.8 percent relative to untreated soil. Yet the corresponding 14-day strength decreased from 797.4 to 630.6 kilopascals. Thus, maximizing the reduction in extractable dissolved organic carbon was not equivalent to maximizing solidification performance. The authors suggest that differences in the location or form of organic-matter transformation influenced subsequent particle-binder interactions, with laccase alone producing a more favorable interfacial condition for cementation while ABTS-assisted treatment extended organic transformation over a broader fraction of the system.</p>
<p>The contrasting effects of ABTS on solidification and dewatering reflect the different structural requirements of the two engineering processes. In composite-binder solidification, performance depends on the development of mechanically effective particle-binder contacts during curing, whereas slurry dewatering depends on aggregate formation and the persistence of water-conducting pathways during filtration and cake consolidation. In compacted soil, strength develops primarily at particle-binder contacts; in slurry, organic matter and mineral particles are dispersed throughout the aqueous phase, providing conditions for ABTS-mediated electron transfer to extend organic modification beyond the immediate enzyme-accessible region. ABTS therefore had opposite engineering effects in the two processes: it reduced solidification performance relative to laccase alone but enhanced prolonged chitosan-based slurry dewatering. The authors conclude that the enzyme-mediator combination should be selected according to the intended engineering process rather than treated as universally additive, and they note that validation with natural humic-rich soils and sediments will further define the range of applicability of these formulation trends.</p>
<p><strong>Subject of Research:</strong> Enzymatic soil pretreatment with laccase and ABTS shows opposite effects on solidification and dewatering of humic-rich soil</p>
<p><strong>Article Title:</strong> Differential effects of ABTS-assisted laccase pretreatment on solidification and dewatering of humic-rich soil</p>
<p><strong>Article References:</strong> Chen, X., Singh, P., Luo, K., Ma, Q., &amp; Jiang, N. (2026). Differential effects of ABTS-assisted laccase pretreatment on solidification and dewatering of humic-rich soil. <em>Frontiers in Bioengineering and Biotechnology, 14</em>, Article 1996007. <a href="https://doi.org/10.3389/fbioe.2026.1996007" rel="noopener noreferrer">https://doi.org/10.3389/fbioe.2026.1996007</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3389/fbioe.2026.1996007" rel="noopener noreferrer">10.3389/fbioe.2026.1996007</a></p>
<p><strong>Keywords:</strong> laccase, ABTS, humic-rich soil, soil solidification, slurry dewatering, redox mediator, geotextile tube, unconfined compressive strength, calcium carbide residue, dissolved organic carbon, enzymatic pretreatment, biogeotechnics</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">310974</post-id>	</item>
		<item>
		<title>Hidden Engineers of the Forest Floor: Shrubs Rewire Soil Carbon and Nutrient Cycling</title>
		<link>https://scienmag.com/hidden-engineers-of-the-forest-floor-shrubs-rewire-soil-carbon-and-nutrient-cycling/</link>
		
		<dc:creator><![CDATA[Chloe Pearson]]></dc:creator>
		<pubDate>Sun, 11 Oct 2026 19:25:31 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[alder buckthorn and soil nitrogen cycling]]></category>
		<category><![CDATA[biogeochemical engineering by forest shrubs]]></category>
		<category><![CDATA[biogeochemistry]]></category>
		<category><![CDATA[carbon sequestration]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[effects of understory plants on soil microbial activity]]></category>
		<category><![CDATA[enzyme activity]]></category>
		<category><![CDATA[European hazel and soil nutrient dynamics]]></category>
		<category><![CDATA[forest ecology]]></category>
		<category><![CDATA[forest ecology and soil nutrient management]]></category>
		<category><![CDATA[forest soil nutrient cycling]]></category>
		<category><![CDATA[litter decomposition]]></category>
		<category><![CDATA[mineral-associated organic matter]]></category>
		<category><![CDATA[nitrogen cycling]]></category>
		<category><![CDATA[Podzols]]></category>
		<category><![CDATA[rowan impact on forest carbon reservoirs]]></category>
		<category><![CDATA[sandy Podzols soil properties in forests]]></category>
		<category><![CDATA[Scots pine]]></category>
		<category><![CDATA[shrub-mediated soil carbon and nitrogen fluxes]]></category>
		<category><![CDATA[shrubs]]></category>
		<category><![CDATA[soil carbon storage in forests]]></category>
		<category><![CDATA[soil organic matter]]></category>
		<category><![CDATA[temperate forest understory species ecological roles]]></category>
		<category><![CDATA[understory shrub influence on soil chemistry]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=262930</guid>

					<description><![CDATA[A study of Polish pine forests shows that hazel, buckthorn, and rowan shrubs each leave distinct biochemical fingerprints on soil carbon storage, nutrient leaching, and enzyme activity, revealing the understory as an active regulator of forest biogeochemistry.]]></description>
										<content:encoded><![CDATA[<p>Beneath the quiet canopy of Scots pine forests in southern Poland, an unassuming cast of understory shrubs is quietly rewriting the rules of soil chemistry. A new study published in the journal Plant and Soil reveals that three common shrub species—European hazel, alder buckthorn, and rowan—do far more than fill the space between trees. They act as active biochemical engineers, dramatically altering how carbon and nitrogen are stored, released, and cycled through one of Earth&#8217;s most important carbon reservoirs: forest soil.</p>
<p>The research, conducted by a team from the University of Agriculture in Krakow and partner institutions, examined forty plots of eighty-year-old pine stands in the Olkusz Forest District, some with dense shrub biogroups and some without. The sites sat on sandy Podzols developed from fluvioglacial sands, with nearly identical texture across plots—roughly 88 percent sand—which allowed the researchers to isolate the effect of shrub identity from confounding soil factors. Mean annual temperature at the sites is 7.1 degrees Celsius, with 737 millimeters of yearly precipitation, a typical temperate setting for these widespread European understory species.</p>
<p>What the team found challenges a long-standing assumption in forest ecology. Shrubs have often been treated as structural bystanders—green filler beneath the canopy. Instead, the study shows they are powerful regulators of soil organic matter, the heterogeneous mixture of plant and microbial residues that determines soil fertility, water retention, and the planet&#8217;s capacity to lock away atmospheric carbon. Soils beneath all three shrub species contained significantly more total carbon and nitrogen than pure pine stands, along with higher concentrations of dissolved organic carbon and nitrogen, the mobile compounds that feed soil microbes and transport nutrients downward through the profile.</p>
<p>The key to understanding these effects lies in how soil organic matter is fractionated. The researchers used a density-based physical separation technique, employing a heavy sodium metatungstate solution to divide organic matter into a free light fraction, an occluded light fraction released by sonication, and a mineral-associated fraction. Each fraction tells a different story about time. The light fractions consist of recently shed leaf litter and fine roots that decompose within months to years, fueling rapid microbial activity. The mineral-associated fraction, by contrast, represents organic matter bound to clay and mineral surfaces—a far more stable pool that can persist for decades or centuries and underpins long-term carbon sequestration.</p>
<p>The results showed a striking species-specific signature. European hazel emerged as the strongest soil modifier, significantly boosting carbon and nitrogen in both light fractions, elevating the activity of carbon-degrading enzymes such as beta-glucosidase, beta-D-cellobiosidase, and beta-xylosidase, and increasing the mobility of dissolved nutrients. Alder buckthorn produced the highest dissolved organic carbon concentrations and the greatest sums of dissolved cations and anions, indicating intensified leaching and nutrient turnover—though it also produced the most acidic soils. Rowan took a different path entirely: its soils showed the highest carbon and nitrogen accumulation in the mineral-associated fraction, and the greatest dehydrogenase activity, a marker of overall microbial metabolism, suggesting a role in longer-term carbon stabilization rather than short-term nutrient flushing.</p>
<p>Statistical modeling reinforced the mechanistic story. Multiple linear regression showed that carbon in the free light fraction was strongly predicted by total soil carbon and nitrogen, with the model explaining nearly 89 percent of the variance. Yet the mineral-associated fraction responded only moderately, and the occluded fraction barely at all—confirming the researchers&#8217; hypothesis that shrubs primarily influence the labile, fast-cycling pools while the stabilized pools remain governed by slower processes of microbial processing and mineral binding. A principal component analysis, capturing 65 percent of total variance, cleanly separated hazel- and buckthorn-influenced soils, with their high organic matter content and enzyme activity, from pure pine soils clustered at the low end of the biochemical spectrum, with rowan soils occupying an intermediate position.</p>
<p>The enzymatic measurements provide some of the most vivid evidence of shrub influence. Six extracellular enzymes were assayed, including those that dismantle cellulose and hemicellulose and one, N-acetyl-beta-glucosaminidase, that microbes deploy when mining nitrogen from organic residues. Hazel soils showed the highest activities of the nitrogen-acquiring enzyme and the highest beta-xylosidase and beta-D-cellobiosidase activities, reflecting abundant, nutrient-rich substrates. Rowan soils led in dehydrogenase activity. Pine monoculture soils consistently registered the lowest values across nearly every assay, a sign of limited substrate availability and sluggish organic matter turnover beneath the needle litter.</p>
<p>Why would shrub species differ so sharply? The answer likely lies in litter chemistry and root behavior. Hazel produces nutrient-rich, readily decomposable litter with a lower carbon-to-nitrogen ratio than pine needles, promoting rapid incorporation of organic residues into labile pools and potentially shifting microbial communities from slower, fungal-dominated decomposition toward faster bacterial processing. Root exudates—sugars and organic acids released by living roots—further stimulate distinct microbial processes in the rhizosphere. Buckthorn&#8217;s pronounced leaching effect suggests its litter releases highly soluble compounds, while rowan&#8217;s comparatively modest litter inputs may explain its weaker but more selective influence on stabilized carbon pools.</p>
<p>The broader implications reach into climate science and forest management. Soil holds more carbon than the atmosphere and vegetation combined, and the balance between fast-cycling labile fractions and slow mineral-stabilized pools determines whether that carbon stays put. The study suggests that ongoing shrub expansion in pine-dominated forests—driven by canopy disturbances, changing light regimes, and management decisions—could accelerate nutrient cycling and increase vertical transport of dissolved carbon, with consequences for nutrient retention and ecosystem carbon budgets that depend on which shrub species moves in. Because mineral-associated pools showed such inertia, short-term vegetation shifts will be recorded first in the labile fractions, making these fractions sensitive early-warning indicators of change.</p>
<p>The authors note that this is the first study to directly couple physical organic matter fractionation, dissolved organic matter dynamics, and enzymatic activity across different understory shrub species in temperate pine forests. They caution that microbial communities were not directly assessed, and they call for future work integrating microbial community analysis, shrub functional traits, and long-term observation. But the central message is already clear: the shrub layer is not scenery. It is a working part of the forest&#8217;s biochemical machinery, and the identity of the species that occupy it may help decide how much carbon temperate forests store, and for how long.</p>
<p><strong>Subject of Research:</strong> Effects of understory shrub species on soil organic matter fractionation and biochemical processes in temperate pine forests</p>
<p><strong>Article Title:</strong> Effect of shrub vegetation on soil organic matter fractionation and soil biochemical processes</p>
<p><strong>Article References:</strong> Lasota, J., Kaczorek, D., Delgado-Moreira, M. I., &amp; Błońska, E. (2026). Effect of shrub vegetation on soil organic matter fractionation and soil biochemical processes. <em>Plant and Soil</em>. <a href="https://doi.org/10.1007/s11104-026-09061-x" rel="noopener noreferrer">https://doi.org/10.1007/s11104-026-09061-x</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s11104-026-09061-x" rel="noopener noreferrer">10.1007/s11104-026-09061-x</a></p>
<p><strong>Keywords:</strong> soil organic matter, shrubs, carbon sequestration, dissolved organic carbon, enzyme activity, nitrogen cycling, Scots pine, Podzols, forest ecology, mineral-associated organic matter, litter decomposition, biogeochemistry</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">262930</post-id>	</item>
		<item>
		<title>Warming Seas Push Carbon Into Microbial Loop, Study of Red Sea Finds</title>
		<link>https://scienmag.com/warming-seas-push-carbon-into-microbial-loop-study-of-red-sea-finds/</link>
		
		<dc:creator><![CDATA[Morgan Morrow]]></dc:creator>
		<pubDate>Sat, 10 Oct 2026 01:39:38 +0000</pubDate>
				<category><![CDATA[Marine]]></category>
		<category><![CDATA[bacterial growth efficiency]]></category>
		<category><![CDATA[bacterial respiration]]></category>
		<category><![CDATA[biological carbon pump]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[dissolved organic carbon in Red Sea]]></category>
		<category><![CDATA[effects of climate change on marine carbon sequestration]]></category>
		<category><![CDATA[Gulf of Aqaba]]></category>
		<category><![CDATA[Gulf of Aqaba environmental study]]></category>
		<category><![CDATA[impact of temperature on phytoplankton carbon fixation]]></category>
		<category><![CDATA[marine carbon cycle]]></category>
		<category><![CDATA[microbial activity and organic matter recycling]]></category>
		<category><![CDATA[microbial loop]]></category>
		<category><![CDATA[microbial loop in warming seas]]></category>
		<category><![CDATA[microbial respiration of oceanic carbon]]></category>
		<category><![CDATA[ocean carbon cycle]]></category>
		<category><![CDATA[ocean warming]]></category>
		<category><![CDATA[ocean's biological carbon pump efficiency]]></category>
		<category><![CDATA[oligotrophic ocean]]></category>
		<category><![CDATA[primary production]]></category>
		<category><![CDATA[Red Sea]]></category>
		<category><![CDATA[Red Sea ecosystem and climate interactions]]></category>
		<category><![CDATA[seasonal changes in ocean carbon dynamics]]></category>
		<category><![CDATA[water-column stratification]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=256870</guid>

					<description><![CDATA[A five-month study in the Gulf of Aqaba shows that as summer stratification intensifies, phytoplankton fix less carbon but release a growing share of it as dissolved organic matter that bacteria rapidly respire near the surface, potentially weakening the ocean's capacity to store carbon at depth.]]></description>
										<content:encoded><![CDATA[<p>In the warm, sunlit waters of the Gulf of Aqaba at the northern tip of the Red Sea, summer does something quietly profound to the ocean&#8217;s carbon cycle. As the surface warms and the water column settles into a stable, layered state, the microscopic algae that anchor the marine food web slow their carbon fixation, and an ever-larger share of the carbon they do capture leaks out of their cells as dissolved organic material. That dissolved carbon, rather than sinking to the deep sea as particles, is quickly consumed and respired by bacteria near the surface. A new five-month study published in the journal Ocean Science by Eyal Rahav of the Israel Oceanographic and Limnological Research and the University of California, Santa Cruz, and Adina Paytan of the University of California, Santa Cruz, documents this seasonal shift in remarkable quantitative detail, and its implications reach far beyond this small desert-fringed basin.</p>
<p>The ocean is one of the planet&#8217;s most important carbon reservoirs, and the efficiency with which carbon fixed by phytoplankton is transferred from the surface to the deep sea, the so-called biological carbon pump, helps determine how much carbon dioxide the ocean can lock away on climatically relevant timescales. In vast stretches of the open ocean, chronic nutrient scarcity keeps primary production low and dominated by tiny cells such as the cyanobacterium Prochlorococcus. Under these conditions, much of the newly fixed carbon never leaves the surface layer at all. Instead, it is retained and remineralized within the microbial loop, a closed circuit in which bacteria and other heterotrophic microbes rapidly recycle organic matter back into carbon dioxide. The result is a low transfer efficiency: little carbon reaches higher trophic levels or the ocean interior.</p>
<p>The Gulf of Aqaba offers an ideal natural laboratory for studying how this efficiency changes with the seasons. Every winter, deep convective mixing injects nutrients from below into the surface layer, fueling phytoplankton blooms. In summer, the picture reverses. Surface waters warm to between 25 and 28 degrees Celsius, and a sharp vertical temperature gradient isolates the sunlit euphotic zone from the nutrient-rich waters below. During the 2023 study period, from May to September, the researchers measured the mixed layer shoaling from about 45 meters in early summer to just 15 to 20 meters at the height of stratification in July and August. Nutrient concentrations in the upper 100 meters were correspondingly meager: nitrate plus nitrite ranged from below detection to only 0.14 micromoles per liter, orthophosphate hovered between 0.01 and 0.03 micromoles per liter, and the ratio of nitrogen to phosphorus fell well below the canonical Redfield ratio of 16 to 1, pointing to nitrogen limitation of the microbial community.</p>
<p>To track where the carbon actually went, the team used radiocarbon labeling. Seawater samples collected at 20-meter intervals from the surface down to 100 meters were spiked with sodium bicarbonate labeled with carbon-14 and incubated for 24 hours under ambient temperature and light. After incubation, the samples were gently filtered through glass-fiber filters with a nominal pore size of 0.7 micrometers. The carbon-14 retained on the filters measured particulate primary production, the carbon incorporated into algal biomass, while the labeled carbon passing through the filters quantified dissolved primary production, the photosynthate released extracellularly by the cells. Bacterial production was measured separately using tritiated leucine incorporation, and community respiration was estimated from the decline in dissolved oxygen in dark 24-hour incubations monitored with fiber-optic oxygen sensors. From these measurements the team calculated the percentage of extracellular release and the bacterial growth efficiency, the fraction of consumed organic carbon that bacteria convert into their own biomass rather than respire away.</p>
<p>The seasonal trajectory was unambiguous. Depth-integrated particulate primary production collapsed from 1.26 grams of carbon per square meter per day in May to just 0.35 grams per square meter per day as stratification intensified, a decline of more than 70 percent. Surface rates fell from roughly 25 micrograms of carbon per liter per day to about 8. Meanwhile, the fraction of total production released as dissolved organic carbon climbed steadily: the integrated percentage of extracellular release rose from 2.5 percent in May to between 5.7 and 6.4 percent during June through August, and reached 7.4 percent by September. Near the base of the euphotic zone, below 40 to 60 meters, extracellular release in individual samples climbed as high as 20 percent. The authors attribute this to nutrient stress: when carbon fixation outpaces the assimilation of nitrogen and phosphorus, cells exude excess low-molecular-weight photosynthates, effectively leaking carbon-rich, nutrient-poor dissolved organic matter into the surrounding water.</p>
<p>That leaked carbon did not linger. Dissolved primary production, though modest at 0.02 to 0.03 grams of carbon per square meter per day, correlated positively with bacterial production, which ranged from 0.08 to 0.16 grams of carbon per square meter per day and was highest in mid- to late summer. This coupling suggests that freshly released dissolved substrates directly fuel heterotrophic bacteria, forming a tight conduit between algal photosynthesis and microbial consumption. A statistical analysis of all depth-resolved measurements across the five cruises reinforced the picture: dissolved production correlated significantly with bacterial production, while particulate production showed a negative correlation with chlorophyll, indicating that carbon fixation and release track physiological activity rather than standing biomass. Chlorophyll itself was concentrated in a deep chlorophyll maximum between 60 and 100 meters, which the authors interpret as a photo-acclimation maximum, cells packing more chlorophyll per unit biomass under low light, rather than a true biomass maximum.</p>
<p>Perhaps the most consequential finding concerns bacterial growth efficiency. Despite the decline in primary production, bacterial respiration remained substantial throughout the summer, between 0.23 and 0.52 grams of carbon per square meter per day across the upper 100 meters. As a result, bacterial growth efficiency stayed low to moderate, ranging from 13 percent in May and June to 28 to 30 percent later in the season. In other words, for every unit of organic carbon the bacteria processed, the majority was respired back into dissolved inorganic carbon rather than converted into biomass that could enter the food web or sink. The authors argue that in the hyper-oligotrophic, warm, and physically isolated summer water column, nutrient limitation forces bacteria to respire surplus carbon through overflow metabolism to satisfy their nutritional demands while covering high basal metabolic costs. This contrasts with systems such as the Taiwan Strait, where recent work has reported elevated growth efficiencies, suggesting that oligotrophy alone does not dictate bacterial metabolism; substrate quality, stoichiometry, and physical setting all matter.</p>
<p>The authors also addressed a potential methodological concern: because Prochlorococcus cells are smaller than the nominal 0.7-micrometer pore size of glass-fiber filters, some cells might pass through and inflate the dissolved fraction. Prior work, they note, shows that under low-vacuum filtration comparable to their protocol, roughly 95 percent of Prochlorococcus cells are retained, and chlorophyll recovery on glass-fiber filters matches that of finer 0.2-micrometer membranes in oligotrophic waters. Moreover, the seasonal rise in extracellular release tracked changes in nutrient availability and microbial physiology rather than chlorophyll biomass, supporting the interpretation that the increase reflects a genuine physiological response of nutrient-stressed algae rather than a filtration artifact.</p>
<p>The broader significance lies in what this seasonal snapshot implies for a warming ocean. Climate change is intensifying density stratification across low- and mid-latitude seas, and the Gulf of Aqaba&#8217;s summer regime may foreshadow conditions becoming more widespread. If stronger stratification generally shifts carbon allocation from particulate biomass toward dissolved pathways, then more of the ocean&#8217;s primary production will be recycled within the surface microbial loop rather than exported to depth, weakening the biological carbon pump and shortening the residence time of carbon in the ocean&#8217;s upper layers. The authors call for long-term observations and targeted experiments that manipulate stratification, nutrient supply, and temperature, integrated with trait-based ecosystem models, to predict how microbial communities will adjust their carbon processing as oligotrophication progresses. For now, the message from this small corner of the Red Sea is clear: as the sea warms and stratifies, the microbes that dominate its surface waters become increasingly efficient recyclers and increasingly poor couriers of carbon to the deep.</p>
<p><strong>Subject of Research:</strong> Seasonal water-column stratification and microbial carbon cycling in the oligotrophic Gulf of Aqaba, northern Red Sea</p>
<p><strong>Article Title:</strong> Seasonal stratification regulates carbon allocation between particulate and dissolved pathways in the Gulf of Aqaba</p>
<p><strong>Article References:</strong> Rahav, E., &amp; Paytan, A. (2026). Seasonal stratification regulates carbon allocation between particulate and dissolved pathways in the Gulf of Aqaba. <em>Ocean Science, 22</em>(5), 2711-2723. <a href="https://doi.org/10.5194/os-22-2711-2026" rel="noopener noreferrer">https://doi.org/10.5194/os-22-2711-2026</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.5194/os-22-2711-2026" rel="noopener noreferrer">10.5194/os-22-2711-2026</a></p>
<p><strong>Keywords:</strong> ocean carbon cycle, biological carbon pump, Gulf of Aqaba, Red Sea, water-column stratification, primary production, dissolved organic carbon, bacterial respiration, bacterial growth efficiency, microbial loop, oligotrophic ocean, ocean warming</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">256870</post-id>	</item>
		<item>
		<title>Grazing Disturbance Splits Grassland Life Above and Below the Ground</title>
		<link>https://scienmag.com/grazing-disturbance-splits-grassland-life-above-and-below-the-ground/</link>
		
		<dc:creator><![CDATA[Morgan Morrow]]></dc:creator>
		<pubDate>Fri, 09 Oct 2026 20:28:35 +0000</pubDate>
				<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[aboveground versus belowground biodiversity responses]]></category>
		<category><![CDATA[biodiversity patterns in grasslands]]></category>
		<category><![CDATA[community ecology]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[disturbance gradients in grassland ecosystems]]></category>
		<category><![CDATA[Ecosystem Resilience]]></category>
		<category><![CDATA[effects of grazing on plant and belowground ecosystems]]></category>
		<category><![CDATA[Eurasian meadow steppe ecology]]></category>
		<category><![CDATA[global change]]></category>
		<category><![CDATA[grassland ecology]]></category>
		<category><![CDATA[grassland management and conservation]]></category>
		<category><![CDATA[grazing]]></category>
		<category><![CDATA[Grazing disturbance impact on grassland biodiversity]]></category>
		<category><![CDATA[human-driven grassland disturbances]]></category>
		<category><![CDATA[intermediate disturbance hypothesis]]></category>
		<category><![CDATA[Intermediate Disturbance Hypothesis limitations]]></category>
		<category><![CDATA[livestock grazing and soil health]]></category>
		<category><![CDATA[meadow steppe]]></category>
		<category><![CDATA[microbial ecology]]></category>
		<category><![CDATA[multitrophic communities]]></category>
		<category><![CDATA[soil biodiversity]]></category>
		<category><![CDATA[soil ecosystem resilience to grazing]]></category>
		<category><![CDATA[soil microbial diversity under grazing]]></category>
		<category><![CDATA[stress-gradient hypothesis]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=255778</guid>

					<description><![CDATA[A study of the Eurasian meadow steppe shows that plant communities peak in diversity at moderate grazing while soil multitrophic communities follow a different trajectory, revealing that the Intermediate Disturbance Hypothesis does not generalize across trophic compartments.]]></description>
										<content:encoded><![CDATA[<p>For nearly half a century, ecologists have leaned on one of the field&#8217;s most trusted rules of thumb: the Intermediate Disturbance Hypothesis, or IDH. The idea is elegantly simple. Where disturbance is rare, a few dominant species elbow out the competition and diversity stays low. Where disturbance is relentless, only the toughest survivors persist and diversity collapses again. Somewhere in between, at moderate levels of disruption, the greatest number of species can coexist. A new study of the Eurasian meadow steppe, published in Communications Earth &amp; Environment, now delivers a striking caveat to that classic framework: the rule holds for the plants you can see, but it breaks down for the sprawling, invisible web of life beneath the soil.</p>
<p>The research, led by Jinlong Gao and colleagues spanning the Chinese Academy of Sciences and partner institutions, examined a gradient of grazing-related disturbance across the meadow steppe, one of the most extensive grassland ecosystems in Eurasia. Grazing is among the most pervasive human-driven disturbances in grasslands worldwide, reshaping vegetation through defoliation, trampling, and the return of nutrients in dung and urine. Because livestock activity touches nearly every grassland on the continent, understanding how its intensity shapes biodiversity is not an academic curiosity; it is central to managing ecosystems that support herders, store carbon, and regulate water across vast regions.</p>
<p>Above the ground, the findings read like a textbook confirmation of the IDH. Plant communities responded to the disturbance gradient in a unimodal pattern, with diversity, biomass, and stability all peaking at intermediate levels of grazing-related disturbance. In other words, moderately grazed sites hosted the richest and most balanced plant assemblages, while both lightly disturbed and heavily disturbed sites fell short. This is precisely the hump-shaped relationship the hypothesis predicts, and it reinforces the long-standing management intuition that moderate grazing can sustain more diverse and more stable grassland vegetation than either strict exclusion or intensive use.</p>
<p>Below the ground, however, the story took an unexpected turn. Soil multitrophic communities, the combined assemblages of microbes, fungi, and the microscopic animals that feed on them and on each other, did not follow the same hump. Their alpha diversity, the diversity measured within a given site, was essentially insensitive to the disturbance gradient. No matter how hard the grassland was grazed, the number of soil life forms coexisting at a single location changed little. For a field that has often assumed aboveground rules transfer neatly to the soil, this is a consequential result.</p>
<p>Yet the soil communities were not indifferent to grazing; they simply responded along a different axis. Beta diversity, which captures how much community composition differs from place to place, peaked under moderate disturbance. At intermediate grazing intensity, soil communities across the landscape became most dissimilar from one another, suggesting that moderate disturbance reorganizes belowground life in ways that vary from site to site rather than uniformly reducing or enriching it. This spatial differentiation peaked exactly where plant diversity was highest, but the underlying mechanism and trajectory were clearly distinct.</p>
<p>The researchers also probed the architecture of the soil food web itself, mapping the networks of interactions among multitrophic communities. As disturbance increased, network complexity declined, and the character of the remaining connections shifted toward positive associations. In ecological terms, the intricate web of competition, predation, and antagonism that characterizes undisturbed soil gave way to simpler networks dominated by cooperation or mutual tolerance. The authors interpret this pattern as consistent with the stress-gradient hypothesis, the idea that as environmental stress intensifies, organisms increasingly rely on facilitation rather than competition to persist. Severe grazing, in this view, pushes soil communities into a reorganized, more cooperative state.</p>
<p>What could drive such a fundamental divergence between the visible and invisible halves of the grassland? The study points to a likely culprit: the flow of carbon from plants into the soil. Grazing reduces the biomass and productivity of vegetation, and the researchers found corresponding reductions in plant-derived carbon subsidies reaching belowground communities. Dissolved organic carbon, the labile carbon fraction that soil organisms readily consume, was lower under disturbance, and the remaining dissolved organic matter shifted toward more recalcitrant forms that are harder to decompose. In effect, heavy grazing starves the soil food web of its easiest energy source and forces it to subsist on tougher fare, a shift that plausibly explains both the reorganization of interactions and the changing spatial patterns of diversity.</p>
<p>This carbon mechanism matters far beyond the steppe. Soil multitrophic communities are the engines of decomposition, nutrient cycling, and carbon storage in grasslands, and their composition influences how much carbon these ecosystems lock away or release. If grazing decouples the response of plants from the response of soil organisms, then management strategies calibrated solely on vegetation, such as adjusting stocking rates to maximize plant diversity, may fail to safeguard the belowground processes that ultimately sustain the system. The study&#8217;s authors argue that their findings call for integrating belowground multitrophic dynamics into grassland resilience frameworks, particularly under global change, where shifting grazing regimes, altered precipitation, and rising temperatures will interact in ways that aboveground monitoring alone cannot anticipate.</p>
<p>The broader theoretical implication is equally provocative. The Intermediate Disturbance Hypothesis has been applied, debated, and tested across ecosystems from coral reefs to forests, and it has often been assumed to operate as a general law of biodiversity. By demonstrating that it holds for plants but not for soil multitrophic communities within the same landscape, the study delivers one of the clearest empirical demonstrations that disturbance responses are compartment-specific. The coupling between aboveground and belowground worlds, so often invoked in ecosystem science, is not automatic; disturbance can actively sever it, leaving plants and soil life marching to different ecological drumbeats.</p>
<p>For the Eurasian meadow steppe and the millions of hectares of grassland like it, the practical message is one of humility and nuance. Moderate grazing genuinely appears to be a sweet spot for plant diversity and stability, vindicating rotational and light-to-moderate stocking approaches. But the soil beneath those optimally grazed pastures is undergoing its own quiet transformation, with networks simplifying, communities differentiating, and carbon flows weakening in ways that no vegetation survey will reveal. As grasslands face intensifying pressure from livestock production and climate change, the study suggests that resilient management will require looking below the surface, treating the soil food web not as a passive mirror of the vegetation above but as a distinct and dynamic player with its own rules of response.</p>
<p><strong>Subject of Research:</strong> Effects of grazing disturbance on aboveground plant and belowground soil multitrophic communities in the Eurasian meadow steppe</p>
<p><strong>Article Title:</strong> Grazing-related disturbance decouples aboveground and belowground responses in the Eurasian meadow steppe</p>
<p><strong>Article References:</strong> Gao, J., Wu, S., Wang, H., Chen, S., Wang, S., Xu, M., Pan, Q., Han, X., &amp; Zhuang, X. (2026). Grazing-related disturbance decouples aboveground and belowground responses in the Eurasian meadow steppe. <em>Communications Earth &amp;amp; Environment</em>. <a href="https://doi.org/10.1038/s43247-026-04104-8" rel="noopener noreferrer">https://doi.org/10.1038/s43247-026-04104-8</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1038/s43247-026-04104-8" rel="noopener noreferrer">10.1038/s43247-026-04104-8</a></p>
<p><strong>Keywords:</strong> grassland ecology, grazing, Intermediate Disturbance Hypothesis, soil biodiversity, multitrophic communities, meadow steppe, dissolved organic carbon, stress-gradient hypothesis, community ecology, microbial ecology, ecosystem resilience, global change</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">255778</post-id>	</item>
		<item>
		<title>Rivers Carry a Quarter of Land&#8217;s Carbon to the Sea, but the Numbers Remain Shrouded in Uncertainty</title>
		<link>https://scienmag.com/rivers-carry-a-quarter-of-lands-carbon-to-the-sea-but-the-numbers-remain-shrouded-in-uncertainty/</link>
		
		<dc:creator><![CDATA[Violet Maxwell]]></dc:creator>
		<pubDate>Fri, 09 Oct 2026 16:19:03 +0000</pubDate>
				<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[Amazon River]]></category>
		<category><![CDATA[atmospheric carbon venting from rivers]]></category>
		<category><![CDATA[basin-scale carbon export variability]]></category>
		<category><![CDATA[carbon cycle]]></category>
		<category><![CDATA[carbon cycle in freshwater systems]]></category>
		<category><![CDATA[CO2 outgassing]]></category>
		<category><![CDATA[coastal sediment carbon burial]]></category>
		<category><![CDATA[Congo River]]></category>
		<category><![CDATA[dissolved inorganic carbon]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[dissolved organic carbon in rivers]]></category>
		<category><![CDATA[global carbon budget]]></category>
		<category><![CDATA[global carbon budget uncertainties]]></category>
		<category><![CDATA[impact of rain on carbon dissolution]]></category>
		<category><![CDATA[land-to-ocean flux]]></category>
		<category><![CDATA[Machine learning]]></category>
		<category><![CDATA[modeling challenges in riverine carbon flux]]></category>
		<category><![CDATA[particulate organic carbon in waterways]]></category>
		<category><![CDATA[Permafrost]]></category>
		<category><![CDATA[remote sensing]]></category>
		<category><![CDATA[riverine contribution to ocean carbon]]></category>
		<category><![CDATA[riverine land-to-ocean carbon flux]]></category>
		<category><![CDATA[rivers]]></category>
		<category><![CDATA[terrestrial carbon transport to oceans]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=254881</guid>

					<description><![CDATA[A major new review finds that rivers deliver roughly 0.8 to 1.0 petagrams of carbon to the ocean each year, but tropical giants like the Amazon and Congo remain so poorly observed that model estimates diverge by up to fivefold.]]></description>
										<content:encoded><![CDATA[<p>Every year, an enormous conveyor belt of carbon moves silently across the surface of the Earth. Rain falling on forests, grasslands, and mountains dissolves carbon dioxide, leaches organic matter from soils, and grinds down rocks, sending a continuous stream of dissolved and particulate carbon into the world&#8217;s rivers. From there, a portion of this carbon is delivered to the ocean, a portion is buried in sediments, and a surprisingly large fraction is vented straight back into the atmosphere. A new review published in Nature Reviews Earth &amp; Environment by Robert Spencer of Florida State University, Travis Drake of ETH Zurich, Maodian Liu of Peking University, and Peter Raymond of Yale University synthesizes decades of work on this riverine land-to-ocean carbon flux, and its central message is both reassuring and unsettling: the broad outlines of the global flux are now reasonably well constrained, yet the details remain stubbornly uncertain, with model estimates for individual carbon species spanning roughly threefold differences and basin-scale export estimates diverging by as much as a factor of five.</p>
<p>The scale of the terrestrial handoff to inland waters is staggering. The review estimates that land landscapes deliver between 3 and 4 petagrams of carbon per year to rivers, lakes, and streams, a figure comparable to the annual carbon uptake by terrestrial ecosystems or the fossil fuel emissions of entire continents. Yet only a small slice of that carbon ever reaches the sea. The majority is outgassed from inland water surfaces as carbon dioxide and methane before it can complete the journey. This means that rivers are not merely pipes connecting land and ocean; they are reactive biogeochemical reactors, hotspots of microbial metabolism, photochemical degradation, and gas exchange that fundamentally reshape the carbon they carry. Recognizing inland waters as active processors rather than passive conduits has been one of the major conceptual shifts in carbon cycle science over the past two decades, and the new review places that shift at the center of its framework.</p>
<p>When it comes to the flux that actually reaches the ocean, the models converge on a total global export of roughly 0.8 to 1.0 petagrams of carbon per year. That convergence at the global scale, however, masks deep disagreements beneath the surface. The review finds that estimates for individual carbon species, such as dissolved organic carbon, dissolved inorganic carbon, particulate organic carbon, and dissolved CO2, span approximately threefold ranges across the models that were synthesized. At the scale of individual ocean basins, the picture is even murkier: estimated export of some carbon species to the Atlantic and Pacific varies by up to fivefold between models. These discrepancies arise from differences in how models represent source inputs from soils and vegetation, transport processes within river networks, biogeochemical transformations along the aquatic continuum, and the climate and hydrological drivers that govern everything from flood pulses to drought-induced contraction of river networks.</p>
<p>One of the most striking findings in the synthesis concerns the geography of ignorance. The Amazon and Congo rivers together contribute approximately 21 percent of global river discharge, yet these tropical giants remain far less observed than many smaller temperate watersheds in North America and Europe. The world&#8217;s 30 largest rivers by discharge account for roughly half of global cumulative river discharge, meaning that a modest number of well-instrumented stations on major rivers could dramatically improve global flux estimates. But the tropical basins that dominate the discharge statistics are precisely where long-term monitoring is weakest. Dense tropical forests, vast floodplains, political instability, and logistical challenges have all conspired to leave the planet&#8217;s most important carbon arteries under-sampled, even as small, convenient catchments in wealthy temperate countries accumulate decades of high-frequency data.</p>
<p>The review traces the journey of carbon through the aquatic continuum in careful technical detail. Carbon enters rivers through multiple pathways: dissolved organic carbon leached from litter and soil horizons, dissolved inorganic carbon derived from the respiration of soil microbes and the chemical weathering of carbonate and silicate rocks, and particulate organic carbon stripped from landscapes by erosion. Hydrology acts as the master control. Storm events trigger what researchers call pulse-shunt dynamics, in which floods flush accumulated organic matter from soils into streams and rapidly shunt it downstream before it can be processed. The flood pulse concept, originally developed for river-floodplain systems, captures how seasonal inundation of floodplains connects stored carbon to the river channel. Temperature, meanwhile, controls the production of dissolved organic carbon in soils, while hydrology regulates its export, a decoupling that complicates predictions under a warming climate.</p>
<p>Once in the river network, carbon faces a gauntlet of transformations. Sunlight, particularly ultraviolet radiation, photochemically degrades dissolved organic matter, breaking complex molecules into simpler substrates that microbes can rapidly consume, and in some cases converting organic carbon directly to carbon dioxide. Microbial respiration does the same work in the dark. Gas exchange at the air-water interface, governed by turbulence, slope, and flow regime, determines how much of the resulting CO2 escapes to the atmosphere; studies have shown that small, high-energy streams exchange gases far more rapidly than sluggish lowland rivers. Dams interrupt the journey, trapping sediment and organic carbon in reservoirs, where burial can be efficient but where greenhouse gas emissions from reservoir surfaces can also be substantial. Floodplains act as transient storage zones where deposited organic carbon may be mineralized, buried, or remobilized during subsequent floods.</p>
<p>The fate of riverine carbon in the ocean is itself a scientific puzzle. For decades, oceanographers have debated what happens to terrestrial organic matter once it enters the sea. Radiocarbon measurements of dissolved organic carbon in the Atlantic and Pacific have revealed that terrigenous material is far less abundant in the deep ocean than riverine fluxes alone would predict, implying efficient removal near the coast. Recent work suggests that oxidation can camouflage terrestrial organic matter to appear marine-like, and that photochemical processes in coastal waters accelerate its degradation. Yet other studies indicate that terrestrial dissolved organic carbon inputs to the ocean may have been underestimated. Particulate organic carbon, by contrast, can be efficiently buried in marine sediments, particularly in systems like the Bengal fan, where the Himalayan erosional system delivers and buries organic carbon at remarkable rates. The balance between these fates, outgassing, burial, and oceanic export, determines whether rivers represent a net carbon sink or a net source to the atmosphere.</p>
<p>Human activities are actively rewiring this flux. Anthropogenic perturbations have enhanced water and carbon fluxes from land to ocean through land-use change, agricultural liming, and hydrological alteration. Dissolved inorganic carbon and alkalinity exports from large rivers have been increasing, partly in response to acidification recovery and agricultural practices. Domestic wastewater has been identified as an overlooked source of riverine dissolved carbon. Fires prime terrestrial organic carbon for riverine export. In the Arctic, thawing permafrost is mobilizing old, previously frozen carbon into rivers, and recent work has shown that old carbon is being routed from land to the atmosphere by global river systems, a feedback with potentially significant climate implications. Rising dissolved organic carbon concentrations in many northern rivers signal widespread environmental change, while dam construction and eutrophication are shifting the sources and fates of carbon in river-connected coastal wetlands.</p>
<p>The path forward, the authors argue, requires a concerted expansion of observations in precisely the places where data are scarcest. Sensor networks capable of high-frequency, in situ measurements of dissolved organic matter, carbon dioxide, and water chemistry are already transforming temperate catchment science, and deploying them across tropical and Arctic basins would close critical gaps. Remote sensing offers complementary reach: satellites can now retrieve dissolved organic carbon concentrations, particulate organic carbon fluxes, and even the optical color of rivers across the globe, and machine learning approaches trained on these datasets are beginning to fill spatial and temporal holes in the observational record. Integrating these large datasets with mechanistic studies of the biogeochemical processes that modulate carbon export, and embedding both within process-based and knowledge-guided machine learning models, would sharpen predictions of this globally important flux. As the climate warms and human pressures on rivers intensify, the review makes clear that understanding how much carbon rivers deliver to the ocean, and how much they release to the sky, is no longer a niche question for aquatic chemists. It is a first-order problem for the global carbon budget, and one whose answer depends on finally giving the world&#8217;s great rivers the scientific attention their size demands.</p>
<p><strong>Subject of Research:</strong> The global riverine flux of carbon from land to ocean and its uncertainties</p>
<p><strong>Article Title:</strong> The riverine land-to-ocean carbon flux</p>
<p><strong>Article References:</strong> Spencer, R. G. M., Drake, T. W., Liu, M., &amp; Raymond, P. A. (2026). The riverine land-to-ocean carbon flux. <em>Nature Reviews Earth &amp;amp; Environment</em>. <a href="https://doi.org/10.1038/s43017-026-00834-7" rel="noopener noreferrer">https://doi.org/10.1038/s43017-026-00834-7</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1038/s43017-026-00834-7" rel="noopener noreferrer">10.1038/s43017-026-00834-7</a></p>
<p><strong>Keywords:</strong> carbon cycle, rivers, land-to-ocean flux, dissolved organic carbon, dissolved inorganic carbon, CO2 outgassing, Amazon River, Congo River, permafrost, remote sensing, machine learning, global carbon budget</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">254881</post-id>	</item>
		<item>
		<title>Physics-based AI delivers first global picture of carbon cycling in ocean sediments</title>
		<link>https://scienmag.com/physics-based-ai-delivers-first-global-picture-of-carbon-cycling-in-ocean-sediments/</link>
		
		<dc:creator><![CDATA[Violet Maxwell]]></dc:creator>
		<pubDate>Sun, 04 Oct 2026 14:21:45 +0000</pubDate>
				<category><![CDATA[Marine]]></category>
		<category><![CDATA[AI for climate change research]]></category>
		<category><![CDATA[AI-driven environmental modeling]]></category>
		<category><![CDATA[carbon cycle]]></category>
		<category><![CDATA[carbon sequestration]]></category>
		<category><![CDATA[climate modelling]]></category>
		<category><![CDATA[computational challenges in oceanography]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[dissolved organic carbon in ocean sediments]]></category>
		<category><![CDATA[global marine sediment carbon storage prediction]]></category>
		<category><![CDATA[innovative approaches to Earth system modeling]]></category>
		<category><![CDATA[large-scale carbon flux estimation]]></category>
		<category><![CDATA[machine learning emulators]]></category>
		<category><![CDATA[marine sediments]]></category>
		<category><![CDATA[mechanistic models of carbon reactions]]></category>
		<category><![CDATA[mineral sorption]]></category>
		<category><![CDATA[neural networks]]></category>
		<category><![CDATA[Occam's Razor]]></category>
		<category><![CDATA[ocean biogeochemistry]]></category>
		<category><![CDATA[Ocean sediment carbon cycling]]></category>
		<category><![CDATA[oceanic biogeochemical processes]]></category>
		<category><![CDATA[physics-based AI]]></category>
		<category><![CDATA[physics-based artificial intelligence in marine science]]></category>
		<category><![CDATA[sediment mineral surface interactions]]></category>
		<category><![CDATA[University of Manchester]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=235310</guid>

					<description><![CDATA[University of Manchester researchers used physics-based AI emulators to produce the first global-scale quantification of dissolved organic carbon exchange between seawater and marine sediments.]]></description>
										<content:encoded><![CDATA[<p>For decades, one of the most important pieces of Earth&#8217;s carbon puzzle has remained stubbornly out of reach. Beneath the ocean floor, in the thin layer of sediment that blankets the seabed, dissolved organic carbon continuously moves between seawater and solid particles, shaping how much carbon the ocean stores, releases, and locks away over geological timescales. Scientists knew this hidden exchange mattered, but the mechanistic models needed to quantify it were so computationally demanding that running them globally was simply impossible. Now, researchers at The University of Manchester have shown that a carefully engineered physics-based artificial intelligence framework can do what brute-force numerical simulation never could: deliver the first accurate, global-scale predictions of dissolved organic carbon cycling in marine sediments.</p>
<p>The study, published in The Innovation, was led by Dr Peyman Babakhani from the Department of Civil Engineering and Management and carried out in collaboration with Dr Majid Sedighi. Their starting point was an existing mechanistic model, a set of coupled differential equations describing how organic carbon reacts, dissolves, diffuses, and binds to mineral surfaces within sediment columns. Models of this kind are the gold standard for environmental process research because they are grounded in physical and biogeochemical reality. Yet they are also notoriously slow to solve and often numerically unstable when pushed across the enormous diversity of real-world conditions found in the ocean, from shallow coastal shelves to the deepest abyssal plains.</p>
<p>The Manchester team&#8217;s solution was to train AI emulators, machine learning systems designed to reproduce the input-output behaviour of the full mechanistic model at a tiny fraction of the computational cost. Instead of replacing physics with data-driven guesswork, the approach keeps the mechanistic model at its core: the emulator learns directly from the model&#8217;s own solutions, effectively compressing years of expensive simulation into a fast surrogate that can be evaluated millions of times. Once trained, the emulators could be applied across the entire global ocean, predicting dissolved organic carbon behaviour at resolutions and spatial scales that the original numerical model alone could never achieve.</p>
<p>The results quantify, for the first time, the global magnitude of this previously unmeasured carbon pathway. According to the study, 11 percent of the particulate organic carbon arriving at the seafloor is returned to the water column as dissolved organic carbon, while 24 percent becomes sorbed onto mineral surfaces within the sediment. Perhaps most striking of all, the researchers estimate that roughly half of all solid-phase organic carbon in the upper metre of marine sediments originates not from intact particles settling from above, but from dissolved carbon that was once in seawater or porewater and later bound itself to mineral grains. In other words, the dissolved pool is not a footnote to the sediment carbon budget; it is one of its principal architects.</p>
<p>These numbers carry real weight for Earth&#8217;s long-term carbon accounting. Marine sediments hold one of the planet&#8217;s largest reservoirs of organic carbon, and the fraction that escapes remineralisation determines how much carbon is buried for millions of years versus how much cycles back into the ocean and atmosphere. By demonstrating that mineral sorption of dissolved organic carbon supplies about half of the solid-phase carbon stock in the uppermost metre of sediment, the study reshapes how scientists should think about the seafloor&#8217;s role as a carbon sink. A pathway that was too small, too slow, or too complex to resolve in global models turns out to be a first-order control on the planet&#8217;s carbon budget.</p>
<p>What makes the technical achievement even more remarkable is the choice of algorithm. In developing the modelling framework, the researchers systematically compared deep learning architectures, random forest models, and simpler feedforward artificial neural networks. The expectation in much of modern machine learning is that bigger, deeper, more heavily parameterised models perform better. Here, the opposite occurred: the simplest algorithms produced the most accurate predictions. The team found that increasing the complexity of the neural network structures consistently reduced prediction accuracy, a result that offers rare empirical support for the Principle of Parsimony, better known as Occam&#8217;s Razor, within AI model development. When the underlying process is governed by well-defined physics, a lean model that respects that structure can outperform far more elaborate machinery.</p>
<p>Accuracy was not taken on faith. The researchers validated their emulator outputs in two independent ways. First, they compared predictions against low-resolution global maps in regions where the original mechanistic model remained numerically solvable, confirming that the surrogate faithfully reproduced the full model&#8217;s behaviour wherever a ground truth existed. Second, they checked emulator outputs against algebraic solutions for variables with known analytic expressions, providing an exact mathematical benchmark rather than a merely approximate one. This dual validation strategy is what allows the team to describe their global predictions as accurate rather than merely plausible, and it reflects a broader lesson for the use of machine learning in the geosciences: an emulator is only as trustworthy as the evidence that it has genuinely learned the physics it was meant to imitate.</p>
<p>The implications extend well beyond sediment geochemistry. Quantifying carbon budgets across the sediment-water interface has long been recognised as essential for understanding global climate dynamics, but progress has been hindered by exactly the computational limitations this study overcomes. General circulation models, the workhorses of climate projection, cannot currently afford to embed full mechanistic sediment models at every grid cell of the ocean. A fast, scalable, and accurate surrogate changes that calculus. The new AI-based framework can be integrated into global circulation models, allowing sediment carbon processes to be represented explicitly rather than crudely parameterised, and opening the door to systematic exploration of how the ocean&#8217;s carbon reservoirs may respond to warming, acidification, and altered productivity in the coming decades.</p>
<p>The framework also creates new opportunities for evaluating ocean-based climate change mitigation strategies before any real-world intervention is attempted. Dr Babakhani noted that the modelling framework can play a substantial role in testing potential ocean-based climate change mitigation scenarios in silico, adding that with this approach the team can finally explore global-scale carbon cycling processes that were previously impossible to quantify. The ability to run thousands of counterfactual simulations, each asking how sediment carbon storage might shift under a different management or emissions scenario, is precisely the kind of capability that policy-relevant climate science has lacked for the sediment realm.</p>
<p>There is a broader lesson here for how artificial intelligence enters the environmental sciences. Rather than chasing ever-larger architectures trained on ever-larger datasets, the Manchester study suggests that the most powerful role for AI in many geophysical problems is as a disciplined student of mechanistic models, learning their behaviour, compressing their cost, and extending their reach to scales where the underlying equations could never be solved directly. In doing so, physics-based AI has turned an intractable computational problem into an answerable scientific question, and in the process revealed that the quiet chemistry of the seafloor plays a far larger role in Earth&#8217;s carbon cycle than anyone had been able to measure before.</p>
<p><strong>Subject of Research:</strong> Physics-based artificial intelligence modelling of dissolved organic carbon cycling between seawater and marine sediments</p>
<p><strong>Article Title:</strong> Physics based AI unlocks first global predictions of carbon cycling in ocean sediments</p>
<p><strong>Article References:</strong> Physics based AI unlocks first global predictions of carbon cycling in ocean sediments. (n.d.). <a href="https://www.eurekalert.org/news-releases/1143010" rel="noopener noreferrer">Original publication</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> Not provided</p>
<p><strong>Keywords:</strong> dissolved organic carbon, marine sediments, carbon cycle, physics-based AI, machine learning emulators, neural networks, Occam&#x27;s Razor, carbon sequestration, mineral sorption, climate modelling, ocean biogeochemistry, University of Manchester</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">235310</post-id>	</item>
		<item>
		<title>Mixing Sand Into Oily Soil Supercharges Plant-Microbe Cleanup of Petroleum Pollution</title>
		<link>https://scienmag.com/mixing-sand-into-oily-soil-supercharges-plant-microbe-cleanup-of-petroleum-pollution/</link>
		
		<dc:creator><![CDATA[Savannah Blake]]></dc:creator>
		<pubDate>Thu, 01 Oct 2026 15:28:46 +0000</pubDate>
				<category><![CDATA[Climate]]></category>
		<category><![CDATA[bioremediation]]></category>
		<category><![CDATA[Dietzia]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[engineered soil amendments for oil spill cleanup]]></category>
		<category><![CDATA[groundwater protection from petroleum pollutants]]></category>
		<category><![CDATA[Italian ryegrass]]></category>
		<category><![CDATA[loam]]></category>
		<category><![CDATA[long-term soil health after petroleum contamination]]></category>
		<category><![CDATA[microbial enhancement in oily soils]]></category>
		<category><![CDATA[microbial inoculants]]></category>
		<category><![CDATA[oil spill cleanup using soil engineering]]></category>
		<category><![CDATA[Petroleum hydrocarbon soil contamination]]></category>
		<category><![CDATA[petroleum hydrocarbons]]></category>
		<category><![CDATA[phytoremediation]]></category>
		<category><![CDATA[plant-microbe interactions in contaminated soil]]></category>
		<category><![CDATA[rapid bioremediation techniques for petroleum pollution]]></category>
		<category><![CDATA[rhizodegradation]]></category>
		<category><![CDATA[rhizosphere]]></category>
		<category><![CDATA[soil contamination]]></category>
		<category><![CDATA[soil physical properties and pollutant removal efficiency]]></category>
		<category><![CDATA[soil structure and pollutant degradation]]></category>
		<category><![CDATA[soil texture]]></category>
		<category><![CDATA[soil texture modification for bioremediation]]></category>
		<category><![CDATA[sustainable soil remediation methods]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=223422</guid>

					<description><![CDATA[Australian researchers found that blending oil-contaminated soils to an intermediate loamy texture, combined with Italian ryegrass and microbial inoculants, boosted petroleum hydrocarbon removal to as much as 94 percent in six months.]]></description>
										<content:encoded><![CDATA[<p>Petroleum hydrocarbons are among the most stubborn pollutants on Earth. When crude oil is extracted, refined, transported, or stored, spills and leaks leave behind soils saturated with toxic compounds that can destroy soil structure, poison microbes and soil animals, starve plants of nutrients, and slash crop yields. Contaminated ground does not simply sit still, either. Rainwater trickling through oily soil can carry hydrocarbons into groundwater, wind can lift contaminated dust into the air, and crop plants can accumulate petroleum residues in their tissues, creating health risks for people who inhale, ingest, or drink these pollutants. Now, a team of researchers in Australia has shown that one of the most overlooked physical properties of soil, its texture, can be deliberately engineered to dramatically accelerate the natural cleanup of oil-contaminated ground, achieving removal rates of up to 94 percent in just six months.</p>
<p>The study, published in the journal Cleaner Engineering and Technology, was led by Ebhohon Endurance Odion of Deakin University together with Chuxia Lin, Jiaojiao Ma, and Lambert Brau. Rather than focusing solely on the microbes or plants that break down petroleum, the team asked a more fundamental question: does the physical makeup of the soil itself, the balance between fine clay particles and coarse sand grains, control how fast hydrocarbons disappear? The answer, it turns out, is a resounding yes, and the finding could reshape how we remediate oil spills in some of the world&#8217;s most polluted landscapes.</p>
<p>To test this idea, the researchers built a controlled experiment of unusual rigor. They formulated five distinct soil textures by mixing a clayey garden soil with beach sand collected from Williamstown Beach in Melbourne, ranging from pure clay through intermediate loams to pure sand. Each soil was spiked with 50 milliliters of commercial engine oil per kilogram of soil, producing an initial total extractable petroleum hydrocarbon concentration of 45,680 milligrams per kilogram. Crucially, the contamination was dominated by the hard-to-degrade fractions: 26,000 milligrams per kilogram in the C16-C34 range and 19,500 milligrams per kilogram in the C34-C40 range, with only a tiny 180 milligrams per kilogram in the lighter C10-C16 fraction. This mimics the situation in arid oil-producing regions, where volatile short-chain hydrocarbons evaporate quickly and leave behind persistent long-chain residues.</p>
<p>Into each pot went 25 seedlings of Italian ryegrass, Lolium multiflorum, a species chosen for its dense fibrous root system, rapid establishment, and proven tolerance of hydrocarbon stress. Half of the pots also received a blend of two commercial microbial inoculants, RemActiv from Ziltek and Ultra-Archaea from Ultra-Tech International, whose dominant bacterial genera, including Propionibacterium, Clostridium, Sphingomonas, and Ralstonia, were confirmed by DNA sequencing before application. The pots were grown in a randomized block design in a growth chamber at 23 degrees Celsius with a 16-hour photoperiod, watered every two days, and monitored for six months. Hydrocarbon analysis was performed by an accredited laboratory using gas chromatography, while the soil bacterial communities were profiled through 16S rRNA gene sequencing.</p>
<p>The plant growth results revealed a striking sweet spot. The mixed-loam soil containing equal parts clayey soil and sand, designated Type M, produced the tallest plants and by far the greatest biomass, with inoculated plants in that treatment reaching 36.73 grams of fresh root biomass and 37.98 grams of fresh shoot biomass, the highest values in the entire experiment. Deviating from that ratio in either direction reduced growth. Pure sand performed worst of all, hampered not only by its coarse texture but also by a pH of 9, elevated salinity of 628 microsiemens per centimeter, and almost no organic matter or nutrients. Surprisingly, the pure clay soil, despite containing the highest total concentrations of nitrogen, phosphorus, and potassium, also supported relatively poor growth, because nutrients in clay-rich soils become locked away through fixation processes and the oil itself clogs the already restricted pore network, choking off oxygen and water movement.</p>
<p>This nutrient paradox is one of the study&#8217;s most instructive lessons. Total nutrient concentration alone did not predict plant success; accessibility did. In the balanced loam, roots could proliferate freely, oxygen could diffuse, and nutrients could be mineralized and mobilized, partly with the help of the added microbes. In every soil texture, inoculated plants outgrew their uninoculated counterparts, suggesting the inoculants boosted growth by enhancing nutrient mineralization and by quickly degrading the most phytotoxic hydrocarbons, giving seedlings a cleaner start in life.</p>
<p>The microbial sequencing data added another layer of intrigue. Actinobacteria and Proteobacteria dominated all soils, and inoculation consistently increased both the total number of sequence variants and the abundance of known hydrocarbon degraders. But here is the twist: none of the bacterial genera originally present in the commercial inoculants were detected at harvest. The introduced strains had apparently lost the competition with native microbes. Their benefit was instead a kind of microbial starter motor, kick-starting degradation early in the experiment when indigenous degraders were still sluggish, lowering toxicity, and allowing the plants and their native microbial partners to take over.</p>
<p>The chain of causation the researchers uncovered is elegant. Better soil texture produced better root growth. More root biomass released more dissolved organic carbon into the rhizosphere through root exudation and decaying plant debris. The data showed a strong positive relationship between dried root biomass and soil dissolved organic carbon, and an equally tight relationship between that carbon and the abundance of the eleven major hydrocarbon-degrading bacterial genera. In other words, plants feed the exact microbes that eat the pollution, and as those microbes dismantle the hydrocarbons, the soil becomes less toxic, allowing the plants to grow even more. Notably, non-degrading bacteria did not benefit from this carbon windfall, likely because hydrocarbon degraders enjoy a competitive advantage, able to exploit both plant-derived carbon and petroleum itself as food. Among the degraders, the genus Dietzia dominated across all soil types, thriving in the experiment&#8217;s 23-degree, near-neutral conditions, while genera preferring hotter or more acidic conditions, such as Rhodococcus, remained suppressed.</p>
<p>The bottom-line remediation numbers are what make this study genuinely exciting. After six months, uninoculated control soils removed only 15 to 47 percent of their total petroleum hydrocarbons, while inoculated soils achieved removal rates between 29 and 94 percent. The strongest performances came from the intermediate textures, the loamy sand and clayey loam, which offered the best balance of water retention, aeration, oxygen diffusion, nutrient supply, and root penetration. These results align with earlier work showing that loamy sands outperform silty clays for hydrocarbon removal, and they confirm that even the best microbial inoculant cannot compensate for hostile soil physics.</p>
<p>The practical implications reach far beyond the greenhouse. Many of the world&#8217;s oil-producing nations sit in desert and semi-desert regions where coarse, sandy soils dominate and long-chain hydrocarbons persist after the volatile fractions evaporate. Kuwait&#8217;s first Gulf War oil fires inundated 114 square kilometers of desert land, and similar contamination is widespread across oil-producing regions. This study suggests a deceptively simple, cost-effective intervention: blend overly coarse or overly fine contaminated soils toward an intermediate texture, plant hydrocarbon-tolerant grasses, and add an initial microbial boost. The authors are candid about limitations, noting that unplanted controls were not included, so the exact share of hydrocarbon loss attributable to rhizosphere processes versus plant-free dissipation could not be partitioned, and that freshly spiked soils differ from aged field contamination. Future work with naturally contaminated field soils, mixed contaminants such as heavy metals and salinity, and field-scale trials will be needed. But the core message stands: sometimes the key to cleaning up pollution lies not in adding more chemistry or more microbes, but in reshaping the very ground beneath our feet.</p>
<p><strong>Subject of Research:</strong> Enhancing rhizodegradation of mid- to long-chain petroleum hydrocarbons in contaminated soils through soil texture modification, plant growth, and microbial inoculation</p>
<p><strong>Article Title:</strong> Modification of soil texture as a means to enhance rhizodegradation of mid- to long-chain petroleum hydrocarbons in soils</p>
<p><strong>Article References:</strong> Odion, E. E., Lin, C., Ma, J., &amp; Brau, L. (2026). Modification of soil texture as a means to enhance rhizodegradation of mid- to long-chain petroleum hydrocarbons in soils. <em>Cleaner Engineering and Technology, 35</em>, Article 101331. <a href="https://doi.org/10.1016/j.clet.2026.101331" rel="noopener noreferrer">https://doi.org/10.1016/j.clet.2026.101331</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1016/j.clet.2026.101331" rel="noopener noreferrer">10.1016/j.clet.2026.101331</a></p>
<p><strong>Keywords:</strong> soil texture, rhizodegradation, petroleum hydrocarbons, bioremediation, Italian ryegrass, microbial inoculants, rhizosphere, dissolved organic carbon, Dietzia, soil contamination, phytoremediation, loam</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">223422</post-id>	</item>
		<item>
		<title>Brewery Waste Doubles as Stream Cleaner in Wastewater Nutrient Experiment</title>
		<link>https://scienmag.com/brewery-waste-doubles-as-stream-cleaner-in-wastewater-nutrient-experiment/</link>
		
		<dc:creator><![CDATA[Chloe Pearson]]></dc:creator>
		<pubDate>Thu, 24 Sep 2026 08:02:06 +0000</pubDate>
				<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[biogeochemistry]]></category>
		<category><![CDATA[biogeochemistry of nutrient removal]]></category>
		<category><![CDATA[biological wastewater treatment innovations]]></category>
		<category><![CDATA[Brewery waste as stream nutrient absorber]]></category>
		<category><![CDATA[diel variability]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[eutrophication]]></category>
		<category><![CDATA[freshwater ecological restoration techniques]]></category>
		<category><![CDATA[heterotrophic microbes]]></category>
		<category><![CDATA[Mediterranean stream]]></category>
		<category><![CDATA[microbial nutrient cycling in streams]]></category>
		<category><![CDATA[nitrate]]></category>
		<category><![CDATA[nitrogen uptake]]></category>
		<category><![CDATA[nutrient stoichiometry]]></category>
		<category><![CDATA[nutrient stoichiometry in microbial communities]]></category>
		<category><![CDATA[organic carbon addition in freshwater ecosystems]]></category>
		<category><![CDATA[phosphorus uptake]]></category>
		<category><![CDATA[role of heterotrophic bacteria in nutrient removal]]></category>
		<category><![CDATA[stream ecology]]></category>
		<category><![CDATA[stream water chemistry monitoring]]></category>
		<category><![CDATA[sustainable waste reuse in water quality improvement]]></category>
		<category><![CDATA[use of brewery by-products in ecological experiments]]></category>
		<category><![CDATA[wastewater effluent]]></category>
		<category><![CDATA[wastewater treatment plant effluent management]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=212270</guid>

					<description><![CDATA[Researchers in Spain enriched a wastewater-fed stream with brewery-derived dissolved organic carbon and found that the addition shifted the reach from a net nitrogen source to a nitrogen sink, though total nutrient export fell by less than fifteen percent.]]></description>
										<content:encoded><![CDATA[<p>In a small Mediterranean headwater stream in Catalonia, a team of freshwater ecologists has run one of the most controlled tests to date of a deceptively simple idea: that adding a dash of biologically available carbon to a nutrient-choked stream could coax its microbial communities into absorbing more of the nitrogen and phosphorus pouring out of a wastewater treatment plant. The experiment, led by David Pineda-Morante of the Centre d&#8217;Estudis Avançats de Blanes (CEAB-CSIC) and published in the journal Biogeochemistry, harnessed an unlikely source of that carbon—a dissolved organic matter solution derived from brewery by-product, generously supplied by the La Pirata Brewing company. Over four consecutive days, the researchers injected this carbon-rich brew into a stream fed exclusively by treatment plant effluent, then tracked the chemistry of the water hour by hour at three points along the channel.</p>
<p>The logic behind the experiment rests on a fundamental constraint of microbial life: stoichiometry. Heterotrophic bacteria—the workhorses of nutrient removal in streams—need carbon, nitrogen, and phosphorus in roughly balanced proportions to build biomass and fuel respiration. Wastewater treatment plant effluents disrupt that balance. They deliver heavy loads of dissolved inorganic nitrogen and soluble reactive phosphorus, but comparatively little bioavailable dissolved organic carbon. The result is a stream in which microbes are, in effect, starving for carbon while awash in nutrients, a condition that constrains their capacity to take up nitrogen and phosphorus and allows those nutrients to travel unimpeded downstream, where they can fuel algal blooms, oxygen depletion, and coastal eutrophication far from the source.</p>
<p>Pineda-Morante and colleagues—including Miquel Ribot, Susana Bernal, Anna Lupon, Sara Castelar, Esperança Gacia, Stephanie N. Merbt, Helena Guasch, and Eugènia Martí at CEAB-CSIC, together with Francesc Sabater at the University of Barcelona—began with a careful stoichiometric diagnosis of the receiving stream. Their analysis suggested that heterotrophic nutrient uptake in this system was constrained by both dissolved organic carbon and dissolved inorganic nitrogen, relative to an abundant supply of soluble reactive phosphorus. In other words, phosphorus was not the limiting resource here; carbon and nitrogen were. That diagnosis shaped the team&#8217;s hypothesis: enriching the stream with bioavailable dissolved organic carbon should partially relieve the carbon constraint, stimulate heterotrophic activity, and thereby enhance the uptake of both nitrogen and phosphorus within the stream reach itself.</p>
<p>What followed was a reach-scale enrichment of the kind that has become a gold standard in stream biogeochemistry. The researchers continuously dosed the stream with the brewery-derived dissolved organic matter solution for four days, while collecting hourly water samples from one station upstream of the injection point and two stations downstream. This high-frequency sampling design was essential for capturing a phenomenon that shorter, coarser studies routinely miss: the pronounced day–night rhythm, or diel variability, in stream nutrient processing. Streams are not chemically static. Photosynthesis by benthic algae during daylight hours and respiration by microbes around the clock generate cycles in oxygen, pH, and nutrient demand that can shift the apparent behavior of a reach from hour to hour.</p>
<p>The response to carbon enrichment was rapid and, in places, dramatic. Within the first meters downstream of the injection point, the team observed strong net removal of dissolved organic carbon, coinciding with pronounced oxygen depletion and the visible development of benthic microbial mats. Those mats—dense communities of bacteria and algae colonizing the streambed—were, in effect, the physical signature of a microbial economy suddenly flush with its limiting resource. The influx of carbon triggered a surge in heterotrophic demand, and the microbial community consumed the added carbon quickly enough to draw down oxygen concentrations in the water flowing over the mats, a classic indication of intense aerobic respiration.</p>
<p>Most consequentially for water quality, the stream reach flipped its functional identity. Before enrichment, the reach acted as a net source of dissolved inorganic nitrogen, meaning more nitrogen exited the reach than entered it—a counterintuitive but well-documented behavior in effluent-dominated streams, where internal processes such as mineralization can release more nitrogen than the reach retains. During the enrichment, that pattern reversed: the reach became a net sink for dissolved inorganic nitrogen, driven mainly by enhanced nitrate uptake. Nitrate, the most abundant and mobile form of nitrogen in most effluents, is notoriously difficult for streams to retain, so a carbon-triggered boost in nitrate uptake is precisely the outcome a nutrient manager would hope to see.</p>
<p>Not every nutrient responded equally, however, and the nuances matter. Ammonium uptake showed a weaker, more spatially localized, and more clearly diel-dependent response, waxing and waning with the daily light cycle rather than increasing uniformly. Soluble reactive phosphorus uptake, meanwhile, showed no clear effect of the carbon addition at all. That outcome is consistent with the team&#8217;s initial stoichiometric diagnosis: because phosphorus was already abundant relative to carbon and nitrogen in this stream, relieving the carbon limitation did not create additional phosphorus demand. Microbes with ample phosphorus and newly available carbon directed their extra assimilatory capacity toward nitrogen, particularly nitrate, rather than toward phosphorus.</p>
<p>The study also delivers a sobering reality check. Despite the enhanced local uptake within the dosed reach, the whole-reach reduction in nitrogen and phosphorus export remained below fifteen percent relative to the total nutrient loads delivered by the wastewater treatment plant. In other words, even a four-day, deliberately generous carbon subsidy that visibly transformed the streambed could only trim a modest fraction of the nutrient export leaving the system. Effluent-dominated streams, the findings imply, cannot simply metabolize their way out of the nutrient loads they receive; the loads are simply too large relative to the residence time and processing capacity of the water moving through the channel. Any carbon-based attenuation strategy would therefore need to be one component of a broader management approach that also addresses nutrient loads at the treatment plant itself.</p>
<p>Yet the experiment&#8217;s most durable contribution may be methodological rather than outcome-based. The authors frame their results as support for using system-specific carbon–nitrogen–phosphorus stoichiometry to guide dissolved-organic-carbon-based nutrient attenuation strategies. Rather than applying a generic carbon-dosing prescription, managers could first diagnose which element limits heterotrophic nutrient processing in a given stream—carbon, nitrogen, or phosphorus—and target the addition accordingly. In the Catalan study stream, the stoichiometric framework correctly anticipated that carbon enrichment would boost nitrate uptake but leave phosphorus uptake largely untouched, a predictive success that suggests the approach could be exported to other effluent-receiving streams with confidence.</p>
<p>The research also highlights how much fine-grained temporal sampling matters for understanding stream function. Because the team sampled hourly across both upstream and downstream stations for four straight days, they could separate the sustained effects of carbon enrichment from the background diel oscillations in uptake that would have confounded a single grab-sample campaign. Ammonium&#8217;s light-dependent response, in particular, would likely have been invisible without that cadence. As freshwater systems worldwide face intensifying pressure from urban effluents, seasonal drought, and warming, studies of this kind—integrating ecological stoichiometry, reach-scale manipulation, and high-frequency sensing—offer a template for diagnosing and, where feasible, engineering the microbial machinery that stands between wastewater and the downstream ecosystems those nutrients would otherwise reach. The work was supported by the Spanish Ministry of Science, Innovation, and Universities through multiple national research projects, and the article is published open access, making the full dataset and methods available to researchers and water managers confronting the same carbon–nutrient imbalances elsewhere.</p>
<p><strong>Subject of Research:</strong> How dissolved organic carbon enrichment alters microbial nitrogen and phosphorus uptake in a stream receiving wastewater treatment plant effluent</p>
<p><strong>Article Title:</strong> Dissolved organic matter addition alters diel nitrogen and phosphorus uptake downstream of a wastewater treatment plant effluent</p>
<p><strong>Article References:</strong> Pineda-Morante, D., Ribot, M., Bernal, S., Lupon, A., Castelar, S., Gacia, E., Merbt, S. N., Sabater, F., Guasch, H., &amp; Martí, E. (2026). Dissolved organic matter addition alters diel nitrogen and phosphorus uptake downstream of a wastewater treatment plant effluent. <em>Biogeochemistry</em>. <a href="https://doi.org/10.1007/s10533-026-01363-7" rel="noopener noreferrer">https://doi.org/10.1007/s10533-026-01363-7</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s10533-026-01363-7" rel="noopener noreferrer">10.1007/s10533-026-01363-7</a></p>
<p><strong>Keywords:</strong> biogeochemistry, wastewater effluent, dissolved organic carbon, nitrogen uptake, phosphorus uptake, nutrient stoichiometry, diel variability, stream ecology, heterotrophic microbes, nitrate, eutrophication, Mediterranean stream</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">212270</post-id>	</item>
		<item>
		<title>Aquaculture runoff may erode mangroves&#8217; iron-shielded carbon stores and flip nitrogen cycling toward recycling</title>
		<link>https://scienmag.com/aquaculture-runoff-may-erode-mangroves-iron-shielded-carbon-stores-and-flip-nitrogen-cycling-toward-recycling/</link>
		
		<dc:creator><![CDATA[Alan Morgan]]></dc:creator>
		<pubDate>Mon, 21 Sep 2026 00:08:25 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[Aquaculture runoff impact on mangrove carbon storage]]></category>
		<category><![CDATA[aquaculture wastewater]]></category>
		<category><![CDATA[blue carbon]]></category>
		<category><![CDATA[blue carbon preservation in coastal ecosystems]]></category>
		<category><![CDATA[coastal water quality]]></category>
		<category><![CDATA[denitrification]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[DNRA]]></category>
		<category><![CDATA[ecological services of mangroves in nutrient filtering]]></category>
		<category><![CDATA[effects of aquaculture wastewater on mangrove ecology]]></category>
		<category><![CDATA[environmental impacts of]]></category>
		<category><![CDATA[Forest Ecosystems]]></category>
		<category><![CDATA[influence of aquaculture on mangrove soil chemistry]]></category>
		<category><![CDATA[iron mineral binding in mangrove soils]]></category>
		<category><![CDATA[iron–organic carbon coupling]]></category>
		<category><![CDATA[mangroves]]></category>
		<category><![CDATA[Maowei Sea]]></category>
		<category><![CDATA[microbial nitrogen cycling in mangroves]]></category>
		<category><![CDATA[microbial processes governing nitrogen in coastal wetlands]]></category>
		<category><![CDATA[mineral armor protecting organic carbon in mangroves]]></category>
		<category><![CDATA[nitrogen cycling]]></category>
		<category><![CDATA[nitrogen transformation in mangrove sediments]]></category>
		<category><![CDATA[soil microbes]]></category>
		<category><![CDATA[vulnerability of mangrove carbon reservoirs to pollution]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=204428</guid>

					<description><![CDATA[A study in the Maowei Sea shows aquaculture wastewater weakens iron-protected carbon storage in mangrove soils and shifts nitrogen cycling from permanent removal toward retention and recycling.]]></description>
										<content:encoded><![CDATA[<p>Mangrove forests are among the most powerful carbon reservoirs on Earth, locking away vast quantities of so-called blue carbon in waterlogged soils where decomposition proceeds slowly. Part of this remarkable preservation depends on chemistry that is easy to overlook: iron minerals in the sediment bind organic molecules and shield them from hungry microbes, creating a mineral armor around carbon that might otherwise escape into the atmosphere. At the same time, mangrove soils act as biological filters for coastal waters, transforming excess nitrogen that drains from farms, towns and fish ponds before it can fuel harmful algal blooms. A new study published in Forest Ecosystems suggests that both of these quiet services may be far more fragile than previously assumed when aquaculture wastewater seeps into the forest, weakening the iron–carbon partnership and rewiring the microbial machinery that governs nitrogen.</p>
<p>The research team, led by scientists from East China Normal University including Zhongzheng Yan, focused on mangrove stands in the Maowei Sea reserve in China&#8217;s Beibu Gulf, a region where shrimp and fish pond operations have long bordered the fringing forests. To capture a gradient of human influence, the researchers selected three contrasting sites. One served as a restored reference, located where nearby pond discharge had ceased roughly nine years before sampling. The other two sites sat directly beside active aquaculture pond systems that continued to release nutrient-rich effluent into the mangrove environment. By comparing soils, porewater chemistry and microbial gene profiles across this gradient, the team could trace how increasing wastewater exposure reshapes the underground processes that determine whether carbon stays buried and whether nitrogen is removed or merely recycled.</p>
<p>The chemical contrasts between the sites were striking. At the most heavily affected location, the concentration of dissolved organic carbon in porewater was approximately 99 percent lower than at the restored reference site. On its face, this might seem paradoxical, because aquaculture wastewater actually imports organic matter and nutrients into the forest. The explanation, the researchers conclude, lies in what those imports do to microbial communities. Nutrient enrichment appears to stimulate microbes to consume the readily available carbon pool far more aggressively, so the standing stock of dissolved organic carbon collapses even as carbon throughput increases. In effect, the wastewater does not simply add material to the soil; it activates an underground economy in which microbes burn through carbon faster than it can accumulate.</p>
<p>This accelerated carbon consumption carried a second, more consequential consequence: a shift toward more reducing conditions in the soil. As microbes devour oxygen and other oxidized compounds while processing organic matter, the sediment chemistry becomes progressively more anoxic and chemically reduced. That matters enormously for iron-bound carbon, because the protective coupling between organic matter and iron minerals depends on the oxidation state of the iron itself. Under increasingly reducing conditions, the mineral shields begin to destabilize, releasing previously protected organic carbon back into the microbial feeding ground. The study found that this enhanced consumption was associated with, and likely contributed to, the more reducing soil environment, together loosening the iron–organic carbon coupling that underpins long-term carbon storage.</p>
<p>The quantitative evidence for this destabilization is compelling. Around mangrove roots, the relatively persistent pool of organic carbon associated with crystalline iron minerals was 67 percent to 76 percent smaller at the two disturbed sites than at the restored reference. Crystalline iron oxides are among the most stable binding partners for organic matter, so a loss of this magnitude represents a substantial drawdown of the carbon that mangrove soils can preserve on decadal to centennial timescales. Intriguingly, carbon associated with a more reactive form of iron increased at the most affected site. The researchers interpret this as evidence of a fundamental shift in the carbon cycle: away from durable, mineral-protected storage and toward a more labile, less stable regime in which carbon circulates rapidly and remains vulnerable to microbial oxidation and eventual release as carbon dioxide.</p>
<p>The study&#8217;s second major finding concerns nitrogen, the nutrient that mangroves famously help scrub from coastal waters. Microbes handle nitrate through two principal pathways. Denitrification converts nitrate into gaseous forms of nitrogen that escape to the atmosphere, permanently removing it from the ecosystem. A competing pathway, dissimilatory nitrate reduction to ammonium, known as DNRA, instead converts nitrate into ammonium, keeping the nitrogen within the soil and making it available again to plants and microbes. The microbial gene evidence gathered in the Maowei Sea indicated that both pathways became active simultaneously under aquaculture stress, but with a telling emphasis: the balance appeared to tilt toward ammonium retention and internal recycling rather than permanent removal.</p>
<p>If that shift holds, the implications for coastal water quality could be significant. A mangrove forest functioning primarily as a nitrogen recycler acts more like a holding buffer than a sink, retaining reactive nitrogen within the ecosystem instead of eliminating the excess that flows in from aquaculture and other land uses. Under heavy nutrient loading, such a forest may no longer deliver the water-purifying service that coastal managers often count on, and ammonium retained in the soil could continue to fuel microbial activity and further carbon loss, linking the nitrogen and carbon findings into a self-reinforcing loop of change.</p>
<p>Among the study&#8217;s most practically interesting results is the identification of a marked transition in nitrogen cycling behavior around a dissolved organic carbon concentration of approximately 32 milligrams per liter. Below and above this porewater threshold, the microbial community&#8217;s nitrogen processing strategy appeared to differ noticeably, suggesting that DOC could serve as an early-warning signal of ecosystem state change. The authors are careful, however, to frame this value as a potential site-specific indicator rather than a universal rule. Because DOC dynamics vary with climate, sediment type, tidal regime and forest history, further studies across other mangrove systems will be needed before such a number can be confidently adopted as a general management threshold.</p>
<p>Taken together, the findings sketch a coherent mechanistic chain from aquaculture discharge to diminished carbon durability. Nutrient-rich wastewater stimulates microbial carbon consumption; intensified consumption drives soil chemistry toward more reducing conditions; reducing conditions destabilize the crystalline iron minerals that guard persistent organic carbon; and the resulting carbon mobilization feeds back into microbial activity while nitrogen pathways pivot from removal to retention. The two ecosystem services at stake, durable blue carbon storage and coastal nitrogen regulation, are therefore not independent functions but tightly coupled outcomes of the same underground chemistry and microbial ecology. Disturbing one leg of the system inevitably strains the other.</p>
<p>For coastal policymakers and restoration practitioners, the study underscores the importance of managing aquaculture discharge before it reaches mangrove soils, whether through improved pond effluent treatment, buffer zones or strategic placement of restoration sites away from active discharge. It also argues for monitoring programs that look beyond conventional water-quality parameters to track carbon–iron–microbial interactions directly, since the earliest signs of functional decline appear in porewater chemistry and gene profiles rather than in the visible health of the trees. As aquaculture continues to expand across tropical and subtropical coastlines worldwide, understanding these hidden soil processes may prove essential to preserving the blue carbon and nutrient-filtering benefits that mangrove forests quietly provide.</p>
<p><strong>Subject of Research:</strong> The effects of aquaculture wastewater on iron-bound organic carbon stabilization and microbial nitrogen cycling in mangrove soils</p>
<p><strong>Article Title:</strong> Aquaculture wastewater may weaken mangroves’ iron-based carbon storage and shift nitrogen cycling toward recycling</p>
<p><strong>Article References:</strong> Aquaculture wastewater may weaken mangroves’ iron-based carbon storage and shift nitrogen cycling toward recycling. (n.d.). <a href="https://www.eurekalert.org/news-releases/1144493" rel="noopener noreferrer">Original publication</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> Not provided</p>
<p><strong>Keywords:</strong> mangroves, blue carbon, aquaculture wastewater, iron–organic carbon coupling, dissolved organic carbon, nitrogen cycling, denitrification, DNRA, soil microbes, Maowei Sea, coastal water quality, Forest Ecosystems</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">204428</post-id>	</item>
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		<title>Hidden Viral Killings of Plankton Revealed Through Genetic Traces in Seawater</title>
		<link>https://scienmag.com/hidden-viral-killings-of-plankton-revealed-through-genetic-traces-in-seawater/</link>
		
		<dc:creator><![CDATA[Kristina Jarvis]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 21:09:26 +0000</pubDate>
				<category><![CDATA[Marine]]></category>
		<category><![CDATA[advances in marine genetic analysis]]></category>
		<category><![CDATA[biogeochemical cycles]]></category>
		<category><![CDATA[carbon sequestration]]></category>
		<category><![CDATA[carbon sequestration in oceans]]></category>
		<category><![CDATA[diatoms]]></category>
		<category><![CDATA[digital PCR]]></category>
		<category><![CDATA[dissolved organic carbon]]></category>
		<category><![CDATA[genetic traces in seawater]]></category>
		<category><![CDATA[hidden viral influence on marine ecosystems]]></category>
		<category><![CDATA[impact of plankton death on climate regulation]]></category>
		<category><![CDATA[Marine Ecosystems]]></category>
		<category><![CDATA[Marine plankton mortality]]></category>
		<category><![CDATA[microbial food webs and organic carbon release]]></category>
		<category><![CDATA[ocean biogeochemical cycles]]></category>
		<category><![CDATA[ocean carbon sink mechanisms]]></category>
		<category><![CDATA[ocean viruses]]></category>
		<category><![CDATA[phytoplankton]]></category>
		<category><![CDATA[plankton]]></category>
		<category><![CDATA[plankton viruses and infection]]></category>
		<category><![CDATA[plankton's role in global climate change]]></category>
		<category><![CDATA[raphidophytes]]></category>
		<category><![CDATA[role of phytoplankton in oxygen production]]></category>
		<category><![CDATA[rRNA]]></category>
		<category><![CDATA[viral lysis]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=198632</guid>

					<description><![CDATA[Kyoto University researchers have developed a digital PCR-based method that quantifies viral lysis of plankton by measuring cell-free rRNA in seawater, revealing that cell death peaks during bloom growth rather than decline.]]></description>
										<content:encoded><![CDATA[<p>Marine plankton may be invisible to the naked eye, but their influence on the planet is anything but small. These drifting microscopic organisms anchor the base of nearly every ocean food web, sustain fisheries that feed billions of people, and drive the biogeochemical cycles that regulate Earth&#8217;s climate. Phytoplankton in particular generate roughly half of the oxygen in the atmosphere through photosynthesis and act as vast carbon sinks, drawing carbon dioxide out of surface waters and exporting it to the deep ocean. Yet for all their importance, one of the most fundamental questions about plankton remains remarkably difficult to answer: when and how do these organisms die?</p>
<p>The question matters because plankton death is not simply an endpoint. When plankton cells die, their decomposing remains release dissolved organic carbon into the surrounding seawater, a form of carbon that microbes can transform and that can be stored in the ocean for thousands of years. The fate of this carbon shapes everything from microbial food webs to the ocean&#8217;s long-term capacity to sequester greenhouse gases. Understanding the mechanisms behind plankton mortality is therefore essential for reconstructing how marine ecosystems function and how material flows through them. The trouble is that a single plankton community can consist of hundreds of coexisting species, and pinpointing how many cells within such a crowded assemblage are dying, and at what rate, has long eluded researchers.</p>
<p>A team at Kyoto University has now tackled this challenge by focusing on one of the most pervasive causes of plankton death: viral infection. Viruses are extraordinarily abundant in seawater, and when they infect a plankton cell they often trigger cell lysis, the process by which the cell&#8217;s membrane breaks down and its contents, including genetic material, spill into the environment. This invisible death releases ribosomal RNA, or rRNA, into the water. Rather than trying to count dying cells directly, the researchers reasoned that they could measure the RNA these cells leave behind, turning the genetic debris of viral lysis into a quantitative signal of mortality.</p>
<p>To build such a measurement, the team first grew laboratory cultures of two phytoplankton groups, diatoms and raphidophytes, in a seawater-based medium. They then extracted the rRNA present in the medium and quantified it using digital PCR, a highly sensitive technique capable of counting individual nucleic acid molecules. The approach faced a fundamental obstacle, however: rRNA released into seawater does not persist. It degrades over time, meaning that any measured concentration reflects both the ongoing production of cell-free rRNA and its simultaneous disappearance. Without accounting for degradation, the method would systematically underestimate how much RNA dying cells actually release.</p>
<p>The researchers solved this problem with an elegant trick borrowed from analytical chemistry. They introduced a culture of spike-in ribosomes, a known quantity of ribosomal material that was not produced by the plankton, into the medium and tracked how quickly it degraded. This gave them a degradation rate constant specific to their experimental conditions. They then built a flux model that incorporated both the measured changes in host cell-free rRNA over time and this degradation constant. With both terms in hand, the model could correct for the RNA that had already broken down, making it possible to estimate the true rate of cell lysis at any given moment in the experiment.</p>
<p>The results were striking. Viral infection enhanced the rate of cell-free rRNA production approximately 46-fold compared with uninfected cultures, and subsequent cell lysis boosted it roughly 302-fold. In the non-infected solutions, only very small amounts of rRNA were actively released by living cells, underscoring how strongly lysis signals stand out from the background noise of a healthy population. The method effectively turns viral mortality into a measurable molecular beacon, one that can be detected while the deaths themselves are happening.</p>
<p>Perhaps the most surprising finding emerged from the timing. In the diatom experiment, dissolved rRNA production peaked before the population density began to decline as a result of viral infection. In other words, active cell lysis was already underway while the population as a whole was still growing steadily. From a biogeochemical perspective, this implies that the supply of dissolved organic matter to the environment through cell death may occur primarily during the growth phase of a bloom, rather than during its apparent decline, as conventional observations would suggest. Cells are dying and leaking their contents into the water long before anyone watching the population curve would notice.</p>
<p>We did not expect the temporal decoupling between population declines and cell lysis, says corresponding author Hisashi Endo of Kyoto University. Observing the dynamics of living cells is not enough to evaluate the dissolved organic carbon that phytoplankton contribute to marine environments. The statement carries significant weight for oceanographers who model carbon cycling, because it suggests that mortality-driven carbon fluxes may be systematically misattributed in time if they are inferred solely from changes in cell abundance. Carbon could be flowing into microbial food webs and the deep ocean at moments when blooms appear to be thriving.</p>
<p>The methods developed by the Kyoto team for quantifying this invisible death of plankton offer a valuable new lens for understanding material flows within ecosystems. The researchers are careful to note the study&#8217;s limits. The reasons for plankton mortality are diverse, spanning grazing, nutrient starvation, disease and viral attack, and this study did not distinguish between different causes of cell lysis. The flux model detects death, but not its perpetrator. The team now intends to develop approaches that can track both the impacts and the causes of cell lysis at the species level, a step that would allow ecologists to attribute carbon release to specific pathogens and specific hosts within complex natural communities.</p>
<p>For Endo, the work is the continuation of a long-standing fascination with the viral dark matter of the sea. Since we revealed that a wide variety of viruses are present in seawater, I have been interested in understanding their impact on the ecosystem, he says. Using this research as a starting point, I hope to shed light on the true nature of the plankton ecosystem. As the technique matures and moves from laboratory cultures toward field applications, it could transform how scientists monitor ocean health, refine global carbon models, and appreciate the ceaseless, mostly invisible cycle of life and death playing out in every drop of seawater.</p>
<p><strong>Subject of Research:</strong> Quantifying viral cell lysis of marine plankton using extracellular ribosomal RNA</p>
<p><strong>Article Title:</strong> Dead or alive, plankton support marine ecosystems</p>
<p><strong>Article References:</strong> Dead or alive, plankton support marine ecosystems. (n.d.). <a href="https://www.eurekalert.org/news-releases/1143424" rel="noopener noreferrer">Original publication</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> Not provided</p>
<p><strong>Keywords:</strong> plankton, viral lysis, phytoplankton, rRNA, digital PCR, dissolved organic carbon, marine ecosystems, biogeochemical cycles, diatoms, raphidophytes, carbon sequestration, ocean viruses</p>
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