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	<title>Spartina alterniflora &#8211; Science</title>
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	<title>Spartina alterniflora &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>Hidden Deep Soil Carbon Emerges as a Hidden Cost of Coastal Wetland Restoration</title>
		<link>https://scienmag.com/hidden-deep-soil-carbon-emerges-as-a-hidden-cost-of-coastal-wetland-restoration/</link>
		
		<dc:creator><![CDATA[Drew Townsend]]></dc:creator>
		<pubDate>Sat, 10 Oct 2026 03:39:22 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[blue carbon]]></category>
		<category><![CDATA[blue carbon storage capacity in wetlands]]></category>
		<category><![CDATA[coastal wetland soil carbon dynamics]]></category>
		<category><![CDATA[coastal wetlands]]></category>
		<category><![CDATA[deep horizon biogeochemistry in coastal environments]]></category>
		<category><![CDATA[deep soil microbial activity in restored wetlands]]></category>
		<category><![CDATA[deep tillage]]></category>
		<category><![CDATA[effects of black plastic sheeting on soil health]]></category>
		<category><![CDATA[Hangzhou Bay]]></category>
		<category><![CDATA[hidden carbon loss in wetland restoration]]></category>
		<category><![CDATA[impact of invasive plant removal on soil chemistry]]></category>
		<category><![CDATA[iron-bound carbon]]></category>
		<category><![CDATA[long-term effects of wetland restoration on soil carbon]]></category>
		<category><![CDATA[microbial biomass]]></category>
		<category><![CDATA[microbial response to restoration techniques]]></category>
		<category><![CDATA[plastic mulching]]></category>
		<category><![CDATA[salt level changes in coastal soils]]></category>
		<category><![CDATA[soil biogeochemistry]]></category>
		<category><![CDATA[soil carbon sequestration in coastal ecosystems]]></category>
		<category><![CDATA[soil organic carbon]]></category>
		<category><![CDATA[soil salinity]]></category>
		<category><![CDATA[Spartina alterniflora]]></category>
		<category><![CDATA[underground soil chemistry changes during wetland recovery]]></category>
		<category><![CDATA[wetland restoration]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=257250</guid>

					<description><![CDATA[An 18-month field experiment in Hangzhou Bay shows that plastic mulching during coastal wetland restoration desalinizes the entire soil profile, boosts deep-soil microbial biomass, and coincides with major losses of iron-protected carbon down to one metre.]]></description>
										<content:encoded><![CDATA[<p>Beneath the cordgrass marshes of Hangzhou Bay in eastern China lies a vast, dark reservoir of carbon that scientists have long assumed was safely locked away. A new field experiment suggests that assumption may be dangerously wrong. When restoration crews stripped out invasive plants and covered the ground with black plastic sheeting, the effects rippled far beyond the surface: salt levels plunged through the entire top metre of soil, microbial life surged in deep horizons that were thought to be biologically dormant, and substantial amounts of carbon vanished from the profile. The study, published in the journal Biogeosciences by Jingwen Gao of the Chinese Academy of Forestry and colleagues, is among the first to track how common restoration techniques reshape the hidden chemistry of deep coastal soils.</p>
<p>Coastal wetlands are celebrated as blue carbon powerhouses, capable of storing up to roughly 200 megagrams of carbon per hectare in their top metre of soil. Crucially, about 60 to 70 percent of that carbon sits below 30 centimetres, where waterlogged, oxygen-poor conditions slow decomposition and iron minerals bind organic molecules into stable complexes. Most restoration assessments, however, monitor only vegetation recovery and the top 30 centimetres of soil, implicitly treating everything beneath as inert. The Hangzhou Bay team set out to test whether that assumption holds when management interventions dramatically alter salinity and moisture at the surface.</p>
<p>The researchers established three field conditions in a wetland overrun since the 1980s by the invasive cordgrass Spartina alterniflora. Untouched invaded stands served as the control. In a second set of plots, crews removed all aboveground vegetation and covered the soil with 0.1-millimetre black polyethylene film to suppress regrowth and curb evaporative salt accumulation, a technique known as plastic mulching. In a third set, vegetation was removed and the soil mechanically tilled to 160 centimetres with a rotary cultivator to boost aeration and physical disruption, a technique called deep tillage. Five replicate plots of 20 by 20 metres were established for each treatment, separated by at least 50 metres to minimise spatial interference.</p>
<p>Eighteen months later, the team collected soil cores from each plot and sliced them into five depth intervals spanning 0 to 100 centimetres. The samples were analysed for pH, electrical conductivity, moisture, nitrogen pools, total and organic carbon, microbial biomass, and a suite of iron fractions extracted through sequential chemical procedures. The researchers also quantified iron-bound organic carbon, the fraction of soil carbon locked to iron oxides, and sequenced bacterial 16S rRNA genes from surface layers to characterise community shifts. Statistical models, including partial least squares path modeling, were then used to explore how the measured variables related to one another across depth.</p>
<p>The most striking finding was the sheer reach of plastic mulching. Salinity fell by 43 to 53 percent throughout the entire profile, and electrical conductivity dropped by 45 to 50 percent in deep soils compared with untouched stands. Deep tillage, by contrast, reduced surface salinity by only about 20 percent and had limited effect below. With the osmotic stress of salt lifted, microbial biomass carbon in deep soils under mulching climbed from roughly 25 percent above control levels at 30 to 50 centimetres to more than 100 percent at 50 to 100 centimetres. Meanwhile, microbial biomass in the surface 30 centimetres declined, revealing a wholesale redistribution of microbial life from the surface toward deeper horizons.</p>
<p>That microbial awakening coincided with substantial carbon losses. Total carbon under mulching fell by 19 to 35 percent across the profile relative to the control, and soil organic carbon declined by 34 to 65 percent, with the strongest losses at depth. Total nitrogen dropped even more sharply, by 51 to 74 percent. The carbon declines tracked a parallel weakening of mineral protection: poorly crystalline iron oxides, the highly reactive phases that scavenge organic matter, fell by 30 to 50 percent, and iron-bound organic carbon fell by 35 to 50 percent. Integrated across the full metre of soil, the fixed-depth estimate pointed to an apparent soil carbon stock decline of 65 plus or minus 12 megagrams of carbon per hectare over just 18 months.</p>
<p>The mechanistic story the authors propose centres on what soil scientists call the iron gate. In anaerobic wetland soils, iron oxides form organo-mineral complexes that resist microbial attack, effectively shielding carbon for decades or centuries. Rapid desalinization can alter the solubility and mobility of reactive iron phases through changes in ionic strength and pH, potentially dissolving those protective associations. At the same time, salt-stressed deep soil microbes, once freed from osmotic constraint, may become more active in carbon turnover. The path models were consistent with this picture: mulching was strongly associated with altered soil physicochemical conditions, which in turn were negatively associated with reactive iron pools and with soil organic and iron-bound carbon. In surface soils, bacterial community attributes were linked to carbon retention, while in deep soils, increased microbial biomass covaried with reactive iron decline and lower carbon.</p>
<p>The bacterial sequencing revealed dramatic community reorganisation in the surface layers. Untouched stands harboured elevated abundances of sulfur- and iron-cycling taxa such as Sulfurifustis and Acidibacter, tilled soils were enriched in Nocardioides and Nitrospira, and mulched soils were characterised by Thiobacillus and other taxa. Mantel tests showed that salinity and iron-carbon variables were the strongest correlates of community composition, explaining a large share of the variation. The authors are careful, however, to note the limits of their evidence: sequencing covered only the top 20 centimetres, and no direct measurements of carbon dioxide or methane fluxes, pore-water dissolved organic carbon, iron redox speciation, or lateral hydrological export were made. The lost carbon could have been mineralised to greenhouse gases, leached away as dissolved iron-organic complexes, or simply redistributed within the profile, and the study cannot distinguish among these fates.</p>
<p>Those caveats matter because the numbers are sobering when set against restoration gains. Aboveground biomass in restored coastal wetlands typically accumulates at only about 1 to 3 megagrams of carbon per hectare per year after native vegetation returns. A potential subsoil loss of 65 megagrams over 18 months could therefore dwarf the early carbon benefits of replanting, at least in the short term. Three trajectories remain possible for mulched sites: stabilisation as labile carbon pools are exhausted, deceleration as recovering vegetation rebuilds carbon inputs, or continued decline if weakened iron protection persists. Only multi-year monitoring with direct flux measurements can determine which path these sites actually follow, and whether they function as net atmospheric carbon sources.</p>
<p>The study also carries an important design lesson. Because both managed treatments involved vegetation removal before mulching or tillage, the contrasts reflect responses to integrated field management states rather than isolated single-factor effects, and the single-site results from Hangzhou Bay may not generalise to wetlands with different salinity, tides, or sediment textures. Still, the central message is hard to ignore: the magnitude and spatial extent of hydro-geochemical change, not disturbance intensity alone, appears to govern the fate of deep soil carbon after invasive plant removal. The authors argue that blue carbon accounting frameworks should incorporate full-profile soil monitoring to at least one metre, iron-associated carbon metrics as indicators of mineral protection, and multi-year measurements of gaseous and dissolved carbon fluxes. As coastal restoration accelerates worldwide in the fight against climate change, the invisible carbon beneath the marsh surface may prove to be the most important number nobody was counting.</p>
<p><strong>Subject of Research:</strong> Effects of plastic mulching and deep tillage restoration interventions on deep-soil salinity, microbial biomass, and iron-bound carbon in a Spartina alterniflora-invaded coastal wetland</p>
<p><strong>Article Title:</strong> Profile-wide desalinization is associated with increased deep-soil microbial biomass and reduced iron-bound carbon in coastal wetland restoration</p>
<p><strong>Article References:</strong> Profile-wide desalinization is associated with increased deep-soil microbial biomass and reduced iron-bound carbon in coastal wetland restoration. (n.d.). <a href="https://doi.org/10.5194/bg-23-6671-2026" rel="noopener noreferrer">https://doi.org/10.5194/bg-23-6671-2026</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.5194/bg-23-6671-2026" rel="noopener noreferrer">10.5194/bg-23-6671-2026</a></p>
<p><strong>Keywords:</strong> coastal wetlands, blue carbon, soil organic carbon, iron-bound carbon, Spartina alterniflora, soil salinity, microbial biomass, wetland restoration, deep tillage, plastic mulching, soil biogeochemistry, Hangzhou Bay</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">257250</post-id>	</item>
		<item>
		<title>Rain, Not the River, Drives How Fast Louisiana Marsh Grass Decays</title>
		<link>https://scienmag.com/rain-not-the-river-drives-how-fast-louisiana-marsh-grass-decays/</link>
		
		<dc:creator><![CDATA[Sloane Callahan]]></dc:creator>
		<pubDate>Wed, 30 Sep 2026 20:21:28 +0000</pubDate>
				<category><![CDATA[Climate]]></category>
		<category><![CDATA[brackish marsh]]></category>
		<category><![CDATA[carbon sequestration]]></category>
		<category><![CDATA[coastal Louisiana]]></category>
		<category><![CDATA[ecological consequences of coastal restoration projects]]></category>
		<category><![CDATA[effects of freshwater inflow on marsh plant decay]]></category>
		<category><![CDATA[effects of rising sea levels on Louisiana shoreline]]></category>
		<category><![CDATA[freshwater siphon]]></category>
		<category><![CDATA[impact of hurricanes and erosion on Louisiana wetlands]]></category>
		<category><![CDATA[influence of canals and levees on Mississippi River delta]]></category>
		<category><![CDATA[inundation]]></category>
		<category><![CDATA[land loss]]></category>
		<category><![CDATA[litter decomposition]]></category>
		<category><![CDATA[Louisiana coastal land loss]]></category>
		<category><![CDATA[Mississippi River]]></category>
		<category><![CDATA[precipitation]]></category>
		<category><![CDATA[river diversion impacts on marsh ecology]]></category>
		<category><![CDATA[role of rain versus river in marsh grass decomposition]]></category>
		<category><![CDATA[salinity]]></category>
		<category><![CDATA[sediment delivery and marsh rebuilding efforts]]></category>
		<category><![CDATA[Spartina alterniflora]]></category>
		<category><![CDATA[Spartina alterniflora decomposition in brackish marshes]]></category>
		<category><![CDATA[study of plant decay processes in]]></category>
		<category><![CDATA[wetland restoration]]></category>
		<category><![CDATA[wetland restoration strategies]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=218910</guid>

					<description><![CDATA[A three-year litter bag experiment in coastal Louisiana shows that rainfall and siphon-driven freshening, rather than temperature or salinity alone, control how quickly cordgrass litter decomposes in brackish marshes.]]></description>
										<content:encoded><![CDATA[<p>Coastal Louisiana is losing land at a pace that few places on Earth can match. Since 1932, roughly 5,180 square kilometers of coastal wetlands have vanished beneath the Gulf of Mexico, and without intervention, the state&#8217;s coastline is projected to shed another 2,848 square kilometers over the next fifty years. The causes are a tangle of natural and human forces: hurricanes, erosion, subsidence, and rising seas, all made worse by canals and levees that have cut the Mississippi River off from the delta it built. In response, engineers and ecologists have turned to a strikingly counterintuitive strategy—reconnecting the river to its estuary through diversions and siphons that once again deliver freshwater, nutrients, and sediment to marshes starved of them. But a new study reveals that these restoration projects may be quietly reshaping one of the most fundamental processes in wetland ecology: the decay of dead plants.</p>
<p>Researchers led by Aine O&#8217;Nuanain of Louisiana State University set out to measure how the decomposition of smooth cordgrass, Spartina alterniflora, varies across brackish marshes at different distances from the West Pointe à la Hache freshwater siphon in Plaquemines Parish. The siphon, built in 1991, consists of eight tubes each 183 centimeters in diameter and can push up to 76.5 cubic meters of Mississippi River water per second into wetlands that were historically disconnected from the river. Its stated goals are to raise the ratio of marsh to open water, reduce salinity, and improve growing conditions for saltmeadow cordgrass. Yet the freshwater and nutrients it delivers could also accelerate or slow the breakdown of plant litter—a process that recycles nutrients, builds soil, and ultimately determines whether a marsh can keep pace with rising seas.</p>
<p>Decomposition sits at the heart of marsh survival. In organic-rich marsh soils, the balance between plant production and plant decay controls whether the land surface gains or loses elevation. Fast decay can release carbon to the atmosphere and water, while slow decay allows organic matter to accumulate and support the soil. Prior research has linked decomposition rates to inundation, temperature, salinity, and precipitation, but the picture is messy: some studies find that more flooding speeds decay, others find it slows it, and salinity has been reported to have positive, negative, or negligible effects depending on the marsh. Disentangling these collinear drivers is notoriously difficult, and the effects of river diversions on litter decomposition in brackish and saltwater wetlands had never been well quantified.</p>
<p>The team deployed a classic litter bag experiment at three Spartina alterniflora-dominated sites—WPH1, WPH2, and PS7—located 1.2, 6.2, and 11.5 kilometers from the siphon. Live cordgrass collected near Cocodrie, Louisiana was dried at 60 degrees Celsius, and exactly 25.0 grams of leaves and stems were sealed into each mesh bag. Five bags were strung along a line and staked to the marsh surface at plots 1, 10, 25, 50, and 100 meters from the marsh edge along a transect at each site. The bags sat through two-month deployments in the summers of 2018 and 2019, when the siphon was closed, and 2021, when it was open, for durations of 63 to 65 days. Recovered bags were rinsed over a 125-micron sieve, dried to constant mass, and weighed to the nearest 0.1 milligram to calculate the percentage of litter lost per day and an exponential decay coefficient.</p>
<p>The results defied the researchers&#8217; expectations. Decomposition was fastest in 2021—the year the siphon was running—when rates averaged 1.27 percent of mass lost per day, compared with 1.20 percent in 2018 and 1.15 percent in 2019. But 2021 was also the year with the lowest water temperature, the lowest air temperature, and the lowest salinity, contradicting the common finding that warmer, saltier conditions accelerate decay. Salinity in 2021 averaged just 3.42 practical salinity units, versus 10.93 in 2018 and 8.17 in 2019, a dramatic freshening driven by the combination of siphon discharge and heavy rainfall. When the team ran a formal model selection analysis using the Akaike Information Criterion corrected for small sample size, a single variable emerged as the best predictor of decomposition: precipitation, with a positive relationship and an AIC weight of 0.56.</p>
<p>The explanation lies in the dual role of rain. Precipitation directly wets plant litter on the marsh surface, and wetting is known to enhance microbial breakdown of the labile, easily decomposed fraction of organic matter. Indirectly, rainfall and river discharge both push salinity down, and lower salinity may favor different microbial communities and improve litter quality for decomposers. Because water temperature, salinity, and precipitation were cross-correlated across years, the authors caution that their relative contributions cannot be fully separated. Still, the coincidence of high rainfall, low salinity, and peak decomposition in 2021—when the siphon was open—suggests that freshwater inputs from both sky and river acted together to speed the decay of cordgrass litter.</p>
<p>Among sites, the pattern was equally surprising. The marsh farthest from the siphon, PS7, had the highest decomposition rate at 1.29 percent per day, while the two sites closer to the siphon, WPH1 and WPH2, averaged 1.16 and 1.17 percent per day and did not differ from each other. Elevation and inundation explained this gradient: PS7 sat highest above the water at 0.248 meters NAVD88 and was flooded only 8.90 hours per day on average, whereas WPH1, the lowest site at 0.109 meters, was inundated 15.83 hours per day. Contrary to the prediction that more flooding means faster decay, the driest site decayed fastest. The likely mechanism is oxygen: prolonged flooding starves the marsh surface of air, slowing the metabolism of detritivores and aerobic microbes. Previous work by White and Trapani likewise found that increased tidal inundation reduced Spartina litter decomposition, and the authors note that detritivore activity, which they did not measure directly, may underlie the pattern.</p>
<p>The study has honest limitations. The team could not measure nutrient conditions across sites or years, even though Mississippi River water carries elevated nitrate and ammonia that prior research suggests can accelerate microbial breakdown of organic matter. If nutrient enrichment mattered, its effect should have been strongest at WPH1, closest to the siphon—yet that site did not have the highest decomposition rates, even in 2021. Soil chemistry may also cap how much added nutrients can stimulate decay. Site-specific precipitation and air temperature data were unavailable, and a sonde failure at WPH1 in 2019 forced the researchers to interpolate water temperature and salinity from a nearby station using regression models with r-squared values of 0.98 and 0.51 respectively. These compromises are common in litter bag studies, but they add uncertainty to an already tangled web of correlated drivers.</p>
<p>The broader implications reach into the heart of Louisiana&#8217;s fifty-billion-dollar coastal master plan. River diversions and siphons hold genuine promise for rebuilding land, but this study shows they can also alter the ecological machinery that determines whether rebuilt land persists. Wet years will bring more freshwater runoff into brackish marshes, higher river stages, and more frequent opening of diversions—compounding freshwater conditions and, apparently, accelerating litter decay. Faster decay could undermine the carbon sequestration and soil-building services that make marshes resilient to sea-level rise, a concern other researchers have raised about nutrient influx from rivers. The authors recommend that future restoration monitoring quantify litter decomposition, soil and water nutrients, and—critically—the decay of belowground biomass, which contributes most of the organic matter in marsh soils. As the delta&#8217;s engineers reopen the pipes to the Mississippi, the invisible world of decomposers may prove just as important as the sediment they deliver.</p>
<p><strong>Subject of Research:</strong> Effects of a Mississippi River freshwater siphon and environmental drivers on Spartina alterniflora litter decomposition in Louisiana brackish marshes</p>
<p><strong>Article Title:</strong> Decomposition of Spartina alterniflora (smooth cordgrass) in coastal Louisiana brackish marshes influenced by a freshwater siphon</p>
<p><strong>Article References:</strong> O’Nuanain, A., Benelli, A., Winston, J., Swenson, E. M., López-Duarte, P. C., Roberts, B. J., &amp; Polito, M. J. (2025). Decomposition of Spartina alterniflora (smooth cordgrass) in coastal Louisiana brackish marshes influenced by a freshwater siphon. <em>Discover Ecology, 1</em>(1), Article 16. <a href="https://doi.org/10.1007/s44396-025-00019-4" rel="noopener noreferrer">https://doi.org/10.1007/s44396-025-00019-4</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44396-025-00019-4" rel="noopener noreferrer">10.1007/s44396-025-00019-4</a></p>
<p><strong>Keywords:</strong> Spartina alterniflora, litter decomposition, coastal Louisiana, Mississippi River, freshwater siphon, brackish marsh, wetland restoration, salinity, precipitation, inundation, carbon sequestration, land loss</p>
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