Abstract
Spartina alterniflora, an invasive plant widely distributed in China’s coastal regions, has had a significant impact on the stability of wetland ecosystems and elemental biogeochemical cycles. The invasion of S. alterniflora has been found to lead to the accumulation of sulfides in the soil. The cycling of sulfur and iron in the soil is closely interconnected. Coastal estuarine wetlands are influenced by both freshwater in rivers and seawater tides, as well as the frequent variations in redox conditions caused by tidal fluctuations, which makes the cycling of sulfur and iron in the soil invaded by S. alterniflora more intricate. In this study, field surveys and laboratory experiments were conducted to explore the effects of S. alterniflora invasion and hydrological changes on the cycling of sulfur and iron as well as related functional microorganisms in the soil. The invasion of S. alterniflora showed an increase in soil reduced inorganic sulfur (RIS) components in both high and low marshes of Jiuduansha wetland, with higher content observed in summer and autumn. The tidal simulation experiments revealed abundant sulfate in seawater tidal conditions could promote the formation of acid volatile sulfides (AVS) in the soil of low marshes invaded by S. alterniflora and ensuring the continuous increase in AVS content. Diffusive gradients in-thin-films (DGT) technology indicated the existence of high-concentration soluble S2− enrichment zones in the soil of low marshes invaded by S. alterniflora, which may be related to S. alterniflora root exudates. Tidal action increased the relative abundance of sulfur-reducing bacteria (SRB) in the soil of low marshes, and under the influence of seawater tidal action, SRB exhibited higher relative abundance. However, S. alterniflora might inhibit the activity of iron-reducing bacteria (FeRB) in the soil of low marshes. In conclusion, S. alterniflora may enhance the sulfate reduction rate and promote the formation of free sulfides in tidal salt marsh ecosystems by releasing root exudates that stimulate the activity of SRB, while concurrently inhibiting the activity of FeRB and reducing their competition with SRB. This effect is particularly pronounced in low marshes under seawater tidal conditions. Thus, S. alterniflora is capable of rapidly invading tidal salt marshes by utilizing sulfides effectively.
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References
An SQ, Gu BH, Zhou CF et al (2007) Spartina invasion in China: implications for invasive species management and future research. Weed Res 47:183–191. https://doi.org/10.1111/j.1365-3180.2007.00559.x
Backlund K, Boman A, Fröjdö S, Åström M (2005) An analytical procedure for determination of sulphur species and isotopes in boreal acid sulphate soils and sediments. Agric Food Sci 14:70–82. https://doi.org/10.2137/1459606054224147
Barabanov AA, Bukatov GD, Zakharov VA et al (2006) Kinetic Study of Ethylene Polymerization Over Supported Bis(imino)pyridine Iron (II) Catalysts. Macromol Chem Phys 207:1368–1375. https://doi.org/10.1002/macp.200600122
Beck M, Dellwig O, Holstein JM et al (2008) Sulphate, dissolved organic carbon, nutrients and terminal metabolic products in deep pore waters of an intertidal flat. Biogeochemistry 89:221–238. https://doi.org/10.1007/s10533-008-9215-6
Birnbaum C, Waryszak P, Farrer EC (2021) Direct and Indirect Effects of Climate Change in Coastal Wetlands: Will Climate Change Influence Wetlands by Affecting Plant Invasion? Wetlands 41:59. https://doi.org/10.1007/s13157-021-01456-z
Bolyen E, Rideout JR, Dillon MR et al (2019) Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2. Nat Biotechnol 37:852–857. https://doi.org/10.1038/s41587-019-0209-9
Bu N-S, Qu J-F, Li G et al (2015) Reclamation of coastal salt marshes promoted carbon loss from previously-sequestered soil carbon pool. Ecol Eng 81:335–339. https://doi.org/10.1016/j.ecoleng.2015.04.051
Callahan BJ, McMurdie PJ, Rosen MJ et al (2016) DADA2: High-resolution sample inference from Illumina amplicon data. Nat Methods 13:581–583. https://doi.org/10.1038/nmeth.3869
Cao M, Cui L, Sun H et al (2021) Effects of Spartina alterniflora Invasion on Soil Microbial Community Structure and Ecological Functions. Microorganisms 9:138. https://doi.org/10.3390/microorganisms9010138
Chen S, Zhou Y, Chen Y, Gu J (2018a) fastp: an ultra-fast all-in-one FASTQ preprocessor. Bioinformatics 34:i884–i890. https://doi.org/10.1093/bioinformatics/bty560
Chen W, Zhang S, Li R, Shahabi H (2018b) Performance evaluation of the GIS-based data mining techniques of best-first decision tree, random forest, and naïve Bayes tree for landslide susceptibility modeling. Sci Total Environ 644:1006–1018. https://doi.org/10.1016/j.scitotenv.2018.06.389
Chen Y, Shen L, Huang T et al (2020) Transformation of sulfur species in lake sediments at Ardley Island and Fildes Peninsula, King George Island, Antarctic Peninsula. Sci Total Environ 703:135591. https://doi.org/10.1016/j.scitotenv.2019.135591
Clarke D, Williams S, Jahiruddin M et al (2015) Projections of on-farm salinity in coastal Bangladesh. Environ Sci: Processes Impacts 17:1127–1136. https://doi.org/10.1039/C4EM00682H
Cui L, Berger U, Cao M et al (2023) Conservation and Restoration of Mangroves in Response to Invasion of Spartina alterniflora Based on the MaxEnt Model: A Case Study in China. Forests 14:1220. https://doi.org/10.3390/f14061220
Derry LA, Murray RW (2004) Continental Margins and the Sulfur Cycle. Science 303:1981–1982. https://doi.org/10.1126/science.303.5666.1981
Fang W, Williams PN, Fang X et al (2018) Field-Scale Heterogeneity and Geochemical Regulation of Arsenic, Iron, Lead, and Sulfur Bioavailability in Paddy Soil. Environ Sci Technol 52:12098–12107. https://doi.org/10.1021/acs.est.8b01947
Gao G-F, Li P-F, Zhong J-X et al (2019) Spartina alterniflora invasion alters soil bacterial communities and enhances soil N2O emissions by stimulating soil denitrification in mangrove wetland. Sci Total Environ 653:231–240. https://doi.org/10.1016/j.scitotenv.2018.10.277
Ge Y, Pan H, Zhang J et al (2020) Exotic Spartina alterniflora invasion changes temporal dynamics and composition of spider community in a salt marsh of Yangtze Estuary, China. Estuar Coast Shelf Sci 239:106755. https://doi.org/10.1016/j.ecss.2020.106755
Gedan KB, Kirwan ML, Wolanski E et al (2011) The present and future role of coastal wetland vegetation in protecting shorelines: answering recent challenges to the paradigm. Clim Change 106:7–29. https://doi.org/10.1007/s10584-010-0003-7
Gu J, Luo M, Zhang X et al (2018) Losses of salt marsh in China: Trends, threats and management. Estuar Coast Shelf Sci 214:98–109. https://doi.org/10.1016/j.ecss.2018.09.015
Guiry EJ, Orchard TJ, Needs-Howarth S, Szpak P (2022) Freshwater wetland–driven variation in sulfur isotope compositions: Implications for human paleodiet and ecological research. Front Ecol Evol 10. https://doi.org/10.3389/fevo.2022.953042
Guo W, Cecchetti AR, Wen Y et al (2020) Sulfur Cycle in a Wetland Microcosm: Extended 34S-Stable Isotope Analysis and Mass Balance. Environ Sci Technol 54:5498–5508. https://doi.org/10.1021/acs.est.9b05740
He C, Cheng L, Wang D et al (2021a) Spartina alterniflora raised soil sulfide content by regulating sulfur cycle-associated bacteria in the Jiuduansha Wetland of China. Plant Soil 469:107–121. https://doi.org/10.1007/s11104-021-05154-x
He C, Wang X, Wang D et al (2021b) Impact of Spartina alterniflora invasion on soil bacterial community and associated greenhouse gas emission in the Jiuduansha wetland of China. Appl Soil Ecol 168:104168. https://doi.org/10.1016/j.apsoil.2021.104168
Herbert ER, Boon P, Burgin AJ et al (2015) A global perspective on wetland salinization: ecological consequences of a growing threat to freshwater wetlands. Ecosphere 6:art206. https://doi.org/10.1890/ES14-00534.1
Hines ME, Evans RS, Genthner BRS et al (1999) Molecular phylogenetic and biogeochemical studies of sulfate-reducing bacteria in the rhizosphere of Spartina alterniflora. Appl Environ Microbiol 65:2209–2216
Holmer M, Gribsholt B, Kristensen E (2002) Effects of sea level rise on growth of Spartina anglica and oxygen dynamics in rhizosphere and salt marsh sediments. Mar Ecol Prog Ser 225:197–204. https://doi.org/10.3354/meps225197
Howard RJ, Biagas J, Allain L (2016) Growth of Common Brackish Marsh Macrophytes Under Altered Hydrologic and Salinity Regimes. Wetlands 36:11–20. https://doi.org/10.1007/s13157-015-0711-x
Hsieh YP, Shieh YN (1997) Analysis of reduced inorganic sulfur by diffusion methods: improved apparatus and evaluation for sulfur isotopic studies. Chem Geol 137:255–261. https://doi.org/10.1016/S0009-2541(96)00159-3
Huang Y, Guo H, Chen X et al (2019) Meteorological controls on evapotranspiration over a coastal salt marsh ecosystem under tidal influence. Agric for Meteorol 279:107755. https://doi.org/10.1016/j.agrformet.2019.107755
Huang Y, Chen Z, Tian B et al (2020) Tidal effects on ecosystem CO2 exchange in a Phragmites salt marsh of an intertidal shoal. Agric for Meteorol 292–293:108108. https://doi.org/10.1016/j.agrformet.2020.108108
Jiang M, Sheng Y, Zhao G, Wang W (2021) Coupling mechanisms of S-Fe–P in surface sediments under the stresses of high salinity and heavy metals in coastal rivers. J Soils Sediments 21:3234–3245. https://doi.org/10.1007/s11368-021-02948-5
Johnston SG, Burton ED, Aaso T, Tuckerman G (2014) Sulfur, iron and carbon cycling following hydrological restoration of acidic freshwater wetlands. Chem Geol 371:9–26. https://doi.org/10.1016/j.chemgeo.2014.02.001
Karimian N, Johnston SG, Burton ED (2018) Iron and sulfur cycling in acid sulfate soil wetlands under dynamic redox conditions: A review. Chemosphere 197:803–816. https://doi.org/10.1016/j.chemosphere.2018.01.096
Kirwan ML, Guntenspergen GR, Morris JT (2009) Latitudinal trends in Spartina alterniflora productivity and the response of coastal marshes to global change. Glob Change Biol 15:1982–1989. https://doi.org/10.1111/j.1365-2486.2008.01834.x
Klepac-Ceraj V, Bahr M, Crump BC et al (2004) High overall diversity and dominance of microdiverse relationships in salt marsh sulphate-reducing bacteria. Environ Microbiol 6:686–698. https://doi.org/10.1111/j.1462-2920.2004.00600.x
Koop-Jakobsen K, Mueller P, Meier RJ et al (2018) Plant-Sediment interactions in salt marshes – an optode imaging study of O2, pH, and CO2 gradients in the rhizosphere. Front Plant Sci 9. https://doi.org/10.3389/fpls.2018.00541
LaFond-Hudson S, Johnson NW, Pastor J, Dewey B (2018) Iron sulfide formation on root surfaces controlled by the life cycle of wild rice (Zizania palustris). Biogeochemistry 141:95–106. https://doi.org/10.1007/s10533-018-0491-5
Lalonde K, Mucci A, Ouellet A, Gélinas Y (2012) Preservation of organic matter in sediments promoted by iron. Nature 483:198–200. https://doi.org/10.1038/nature10855
Lamers L, Govers L, Janssen I et al (2013) Sulfide as a soil phytotoxin—a review. Front Plant Sci 4. https://doi.org/10.3389/fpls.2013.00268
Leyden E, Farkaš J, Hutson J, Mosley LM (2023) Controls on sulfide accumulation in coastal soils during simulated sea level rise. Geochim Cosmochim Acta 347:88–101. https://doi.org/10.1016/j.gca.2023.02.018
Li B, Liao C, Zhang X et al (2009) Spartina alterniflora invasions in the Yangtze River estuary, China: An overview of current status and ecosystem effects. Ecol Eng 35:511–520. https://doi.org/10.1016/j.ecoleng.2008.05.013
Li Y, Hua J, He C et al (2023) Spartina alterniflora raised sediment sulfide in a tidal environment and buffered it with iron in the Jiuduansha Wetland. J Soils Sediments. https://doi.org/10.1007/s11368-023-03656-y
Lin W, Chen G, Guo P et al (2015) Remote-Sensed Monitoring of Dominant Plant Species Distribution and Dynamics at Jiuduansha Wetland in Shanghai, China. Remote Sens 7:10227–10241. https://doi.org/10.3390/rs70810227
Liu C, Li P, Xie W et al (2021) Changes of sulfur fractions in sediment following Spartina alterniflora invasion in a seaward direction in a temperate salt marsh, China. Ecol Indic 131:108217. https://doi.org/10.1016/j.ecolind.2021.108217
Lu Q, Bai J, Gao Z et al (2016) Effects of Water Level and Salinity on Total Sulfur Contents in Salt Marsh Soils of the Yellow River Delta, China. Wetlands 36:137–143. https://doi.org/10.1007/s13157-015-0661-3
Lu Q, Bai J, Yan D et al (2020) Sulfur forms in wetland soils with different flooding periods before and after flow-sediment regulation in the Yellow River Delta, China. J Clean Prod 276:122969. https://doi.org/10.1016/j.jclepro.2020.122969
Luo M, Zeng C-S, Tong C et al (2014) Abundance and speciation of iron across a subtropical tidal marsh of the Min River Estuary in the East China Sea. Appl Geochem 45:1–13. https://doi.org/10.1016/j.apgeochem.2014.02.014
Luo M, Zeng C-S, Tong C et al (2016) Iron Reduction Along an Inundation Gradient in a Tidal Sedge (Cyperus malaccensis) Marsh: the Rates, Pathways, and Contributions to Anaerobic Organic Matter Mineralization. Estuar Coast 39:1679–1693. https://doi.org/10.1007/s12237-016-0094-0
Magoč T, Salzberg SL (2011) FLASH: fast length adjustment of short reads to improve genome assemblies. Bioinformatics 27:2957–2963. https://doi.org/10.1093/bioinformatics/btr507
Mandernack KW, Lynch L, Krouse HR, Morgan MD (2000) Sulfur cycling in wetland peat of the New Jersey Pinelands and its effect on stream water chemistry. Geochim Cosmochim Acta 64:3949–3964. https://doi.org/10.1016/S0016-7037(00)00491-9
Mazhar S, Pellegrini E, Contin M et al (2022) Impacts of salinization caused by sea level rise on the biological processes of coastal soils - A review. Front Environ Sci 10. https://doi.org/10.3389/fenvs.2022.909415
Medina-Calderón JH, Mancera-Pineda JE, Castañeda-Moya E, Rivera-Monroy VH (2021) Hydroperiod and salinity interactions control mangrove root dynamics in a karstic oceanic island in the Caribbean Sea (San Andres, Colombia). Front Marine Sci 7. https://doi.org/10.3389/fmars.2020.598132
Mo S, He S, Sang Y et al (2023) Integration of Microbial Transformation Mechanism of Polyphosphate Accumulation and Sulfur Cycle in Subtropical Marine Mangrove Ecosystems with Spartina alterniflora Invasion. Microb Ecol 85:478–494. https://doi.org/10.1007/s00248-022-01979-w
Morris JT, Haley C, Krest R (1996) Effects of Sulfide on Growth and Dimethylsulfoniopropionate (DMSP) Concentration in Spartina Alterniflora. In: Kiene RP, Visscher PT, Keller MD, Kirst GO (eds) Biological and Environmental Chemistry of DMSP and Related Sulfonium Compounds. Springer US, Boston, pp 87–95
Muyzer G, Stams AJM (2008) The ecology and biotechnology of sulphate-reducing bacteria. Nat Rev Microbiol 6:441–454. https://doi.org/10.1038/nrmicro1892
Myrbo A, Swain EB, Johnson NW et al (2017) Increase in Nutrients, Mercury, and Methylmercury as a Consequence of Elevated Sulfate Reduction to Sulfide in Experimental Wetland Mesocosms. J Geophys Res Biogeosci 122:2769–2785. https://doi.org/10.1002/2017JG003788
Neubauer SC, Givler K, Valentine S, Megonigal JP (2005) Seasonal Patterns and Plant-Mediated Controls of Subsurface Wetland Biogeochemistry. Ecology 86:3334–3344. https://doi.org/10.1890/04-1951
Nie M, Wang M, Li B (2009) Effects of salt marsh invasion by Spartina alterniflora on sulfate-reducing bacteria in the Yangtze River estuary, China. Ecol Eng 35:1804–1808. https://doi.org/10.1016/j.ecoleng.2009.08.002
Nie S, Mo S, Gao T et al (2023) Coupling effects of nitrate reduction and sulfur oxidation in a subtropical marine mangrove ecosystem with Spartina alterniflora invasion. Sci Total Environ 862:160930. https://doi.org/10.1016/j.scitotenv.2022.160930
O’brien RM (2007) A Caution Regarding Rules of Thumb for Variance Inflation Factors. Qual Quant 41:673–690. https://doi.org/10.1007/s11135-006-9018-6
Pan F, Liu H, Guo Z et al (2019) Effects of tide and season changes on the iron-sulfur-phosphorus biogeochemistry in sediment porewater of a mangrove coast. J Hydrol 568:686–702. https://doi.org/10.1016/j.jhydrol.2018.11.002
Pellegrini E, Incerti G, Pedersen O et al (2022) Flooding and Soil Properties Control Plant Intra- and Interspecific Interactions in Salt Marshes. Plants 11:1940. https://doi.org/10.3390/plants11151940
Peralta Ogorek LL, Takahashi H, Nakazono M, Pedersen O (2023) The barrier to radial oxygen loss protects roots against hydrogen sulphide intrusion and its toxic effect. New Phytol 238:1825–1837. https://doi.org/10.1111/nph.18883
Poulton SW, Krom MD, Raiswell R (2004) A revised scheme for the reactivity of iron (oxyhydr)oxide minerals towards dissolved sulfide. Geochim Cosmochim Acta 68:3703–3715. https://doi.org/10.1016/j.gca.2004.03.012
Qu Z-L, Liu B, Ma Y et al (2020) The response of the soil bacterial community and function to forest succession caused by forest disease. Funct Ecol 34:2548–2559. https://doi.org/10.1111/1365-2435.13665
Scherer HW (2009) Sulfur in soils. J Plant Nutr Soil Sci 172:326–335. https://doi.org/10.1002/jpln.200900037
Schoepfer VA, Bernhardt ES, Burgin AJ (2014) Iron clad wetlands: Soil iron-sulfur buffering determines coastal wetland response to salt water incursion. J Geophys Res Biogeosci 119:2209–2219. https://doi.org/10.1002/2014JG002739
Seliskar DM, Smart KE, Higashikubo BT, Gallagher JL (2004) Seedling sulfide sensitivity among plant species colonizing Phragmites-infested wetlands. Wetlands 24:426–433. https://doi.org/10.1672/0277-5212(2004)024[0426:SSSAPS]2.0.CO;2
Shang S, Hu S, Liu X et al (2022) Effects of Spartina alterniflora invasion on the community structure and diversity of wetland soil bacteria in the Yellow River Delta. Ecol Evol 12:e8905. https://doi.org/10.1002/ece3.8905
Sheng Y, Sun Q, Shi W et al (2015) Geochemistry of reduced inorganic sulfur, reactive iron, and organic carbon in fluvial and marine surface sediment in the Laizhou Bay region, China. Environ Earth Sci 74:1151–1160. https://doi.org/10.1007/s12665-015-4101-8
Short FT, Kosten S, Morgan PA et al (2016) Impacts of climate change on submerged and emergent wetland plants. Aquat Bot 135:3–17. https://doi.org/10.1016/j.aquabot.2016.06.006
Sim MS, Ono S, Bosak T (2012) Effects of Iron and Nitrogen Limitation on Sulfur Isotope Fractionation during Microbial Sulfate Reduction. Appl Environ Microbiol 78:8368–8376. https://doi.org/10.1128/AEM.01842-12
Stribling JM (1997) The relative importance of sulfate availability in the growth of Spartina alterniflora and Spartina cynosuroides. Aquat Bot 56:131–143. https://doi.org/10.1016/S0304-3770(96)01102-3
Sun Q, Sheng Y, Yang J et al (2016) Dynamic characteristics of sulfur, iron and phosphorus in coastal polluted sediments, north China. Environ Pollut 219:588–595. https://doi.org/10.1016/j.envpol.2016.06.019
Taillefert M, Neuhuber S, Bristow G (2007) The effect of tidal forcing on biogeochemical processes in intertidal salt marsh sediments. Geochem Trans 8:6. https://doi.org/10.1186/1467-4866-8-6
van der Heide T, Temmink RJM, Fivash GS et al (2021) Coastal restoration success via emergent trait-mimicry is context dependent. Biol Cons 264:109373. https://doi.org/10.1016/j.biocon.2021.109373
van der Welle MEW, Cuppens M, Lamers LPM, Roelofs JGM (2006) Detoxifying toxicants: interactions between sulfide and iron toxicity in freshwater wetlands. Environ Toxicol Chem 25:1592–1597. https://doi.org/10.1897/05-283r.1
Van Der Welle MEW, Smolders AJP, Op Den Camp HJM et al (2007) Biogeochemical interactions between iron and sulphate in freshwater wetlands and their implications for interspecific competition between aquatic macrophytes. Freshw Biol 52:434–447. https://doi.org/10.1111/j.1365-2427.2006.01683.x
Wang F, Chapman PM (1999) Biological implications of sulfide in sediment—a review focusing on sediment toxicity. Environ Toxicol Chem 18:2526–2532. https://doi.org/10.1002/etc.5620181120
Wang Z, Zhang H, He C et al (2019) Spatiotemporal variability in soil sulfur storage is changed by exotic Spartina alterniflora in the Jiuduansha Wetland, China. Ecol Eng 133:160–166. https://doi.org/10.1016/j.ecoleng.2019.04.014
Weston NB, Dixon RE, Joye SB (2006) Ramifications of increased salinity in tidal freshwater sediments: Geochemistry and microbial pathways of organic matter mineralization. J Geophys Res: Biogeosciences 111. https://doi.org/10.1029/2005JG000071
Wijsman JWM, Middelburg JJ, Herman PMJ et al (2001) Sulfur and iron speciation in surface sediments along the northwestern margin of the Black Sea. Mar Chem 74:261–278. https://doi.org/10.1016/S0304-4203(01)00019-6
Wilson BJ, Mortazavi B, Kiene RP (2015) Spatial and temporal variability in carbon dioxide and methane exchange at three coastal marshes along a salinity gradient in a northern Gulf of Mexico estuary. Biogeochemistry 123:329–347. https://doi.org/10.1007/s10533-015-0085-4
Xia L, Yang W, Zhao H et al (2015) High Soil Sulfur Promotes Invasion of Exotic Spartina alterniflora into Native Phragmites australis Marsh. CLEAN – Soil Air Water 43:1666–1671. https://doi.org/10.1002/clen.201300883
Yan Z, Xu Y, Zhang Q et al (2019) Decomposition of Spartina alterniflora and concomitant metal release dynamics in a tidal environment. Sci Total Environ 663:867–877. https://doi.org/10.1016/j.scitotenv.2019.01.422
Yang C, Lu G, Chen M et al (2016) Spatial and temporal distributions of sulfur species in paddy soils affected by acid mine drainage in Dabaoshan sulfide mining area, South China. Geoderma 281:21–29. https://doi.org/10.1016/j.geoderma.2016.06.032
Yang J, Paytan A, Yang Y et al (2020) Organic carbon and reduced inorganic sulfur accumulation in subtropical saltmarsh sediments along a dynamic coast, Yancheng, China. J Mar Syst 211:103415. https://doi.org/10.1016/j.jmarsys.2020.103415
Yu X, Yang J, Liu L et al (2015) Effects of Spartina alterniflora invasion on biogenic elements in a subtropical coastal mangrove wetland. Environ Sci Pollut Res 22:3107–3115. https://doi.org/10.1007/s11356-014-3568-2
Zak D, Hupfer M, Cabezas A et al (2021) Sulphate in freshwater ecosystems: A review of sources, biogeochemical cycles, ecotoxicological effects and bioremediation. Earth Sci Rev 212:103446. https://doi.org/10.1016/j.earscirev.2020.103446
Zeleke J, Sheng Q, Wang J-G et al (2013) Effects of Spartina alterniflora invasion on the communities of methanogens and sulfate-reducing bacteria in estuarine marsh sediments. Front Microbiol 4. https://doi.org/10.3389/fmicb.2013.00243
Zhang Q, Yan Z, Li X (2021) Iron plaque formation and rhizosphere iron bacteria in Spartina alterniflora and Phragmites australis on the redoxcline of tidal flat in the Yangtze River Estuary. Geoderma 392:115000. https://doi.org/10.1016/j.geoderma.2021.115000
Zhang Z, Nie S, Sang Y et al (2022) Effects of Spartina alterniflora Invasion on Nitrogen Fixation and Phosphorus Solubilization in a Subtropical Marine Mangrove Ecosystem. Microbiol Spectr 10:e00682-e721. https://doi.org/10.1128/spectrum.00682-21
Zhao Z, Cheng L, He C et al (2022) Spartina alterniflora Invaded Coastal Wetlands by Raising Soil Sulfur Contents: A Meta-Analysis. Water 14:1633. https://doi.org/10.3390/w14101633
Zheng Y, Bu N-S, Long X-E et al (2017) Sulfate reducer and sulfur oxidizer respond differentially to the invasion of Spartina alterniflora in estuarine salt marsh of China. Ecol Eng 99:182–190. https://doi.org/10.1016/j.ecoleng.2016.11.031
Zhou C, An S, Deng Z et al (2009) Sulfur storage changed by exotic Spartina alterniflora in coastal saltmarshes of China. Ecol Eng 35:536–543. https://doi.org/10.1016/j.ecoleng.2008.01.004
Zhu M-X, Liu J, Yang G-P et al (2012) Reactive iron and its buffering capacity towards dissolved sulfide in sediments of Jiaozhou Bay, China. Mar Environ Res 80:46–55. https://doi.org/10.1016/j.marenvres.2012.06.010
Zhu Q, Cochran JK, Heilbrun C et al (2021) Small-Scale geochemical heterogeneities and seasonal variation of iron and sulfide in salt marshes revealed by two-dimensional sensors. Front Earth Sci 9. https://doi.org/10.3389/feart.2021.653698
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This study was financially supported by the Natural Science Foundation of China(41971055). Great thanks to the group who provided invaluable support while the samples were collected.
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Yuanhang Li: conceptualization, methodology, writing — original draft;
Jing Hua: investigation, methodology, writing — original draft, writing — review and editing;
Yanxiang Tao: investigation;
Chiquan He: writing — original draft, writing — review and editing, methodology, supervision.
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Li, Y., Hua, J., Tao, Y. et al. Invasion mechanism of Spartina alterniflora by regulating soil sulfur and iron cycling and microbial composition in the Jiuduansha Wetland. Environ Sci Pollut Res 31, 14775–14790 (2024). https://doi.org/10.1007/s11356-024-32118-2
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DOI: https://doi.org/10.1007/s11356-024-32118-2