Skip to main content

Advertisement

Log in

Conversion of organic carbon from decayed native and invasive plant litter in Jiuduansha wetland and its implications for SOC formation and sequestration

  • Soils, Sec 1 • Soil Organic Matter Dynamics and Nutrient Cycling • Research Article
  • Published:
Journal of Soils and Sediments Aims and scope Submit manuscript

Abstract

Purpose

It is still controversial which type of plant litter is conducive to soil organic carbon (SOC) formation. Here we are to explore the conversion of organic carbon (OC) from decayed plant litter in soil and its influence on final SOC sequestration.

Materials and methods

In situ investigation combined with laboratory soil incubation experiments were conducted in mixing zones dominated by halophytes of Phragmites communis and Spartina alterniflora in the Jiuduansha wetland of the Yangtze River estuary to investigate differences in conversion patterns of OC from two decayed plant litters of different characteristics using traditional physicochemical indicators and stable isotope tracing. Additionally, the mechanism of biotransformation was investigated through analysis of soil microbial community structure.

Results and discussion

Due to the higher content of lignin and cellulose in P. communis litter, the associated soil microbial community was more conducive to the formation of soil humus (HS). By contrast, more easily decomposable S. alterniflora litter induced its related soil microbial community more amenable to mineralization. Consequently, OC from decayed S. alterniflora litter remained in soil for less time than that from decayed P. communis, and the lost OC was more readily converted into CO2. OC from decayed P. communis was degraded very slowly during the early stage of conversion (November), and its longer duration in soil was favorable for HS formation.

Conclusions

Analysis of the conversion of intermediates derived from different types of decayed plants can provide insight into plant litter input and SOC formation, and indicate the whereabouts of lost OC. From the perspective of plant biomass and conversion of plant litter-derived OC, P. communis is more conducive to soil carbon sequestration than S. alterniflora.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

References

  • Berg B, McClaugherty C (2014) Plant litter: decomposition, humus formation, carbon sequestration, third ed. Springer, Berlin Heidelberg

    Google Scholar 

  • Bergey DH, Holt JG (1994) Bergey’s manual of determinative bacteriology, ninth ed. Lippincott Williams & Wilkins, Baltimore

    Google Scholar 

  • Caesar-Tonthat TC, Cochran VL (2000) Soil aggregate stabilization by a saprophytic lignin-decomposing basidiomycete fungus I. Microbiological aspects. Biol Fertil Soils 32:374–380

    Google Scholar 

  • Carter MR, Gregorich EG (2008) Soil sampling and methods of analysis. CRC Press, Florida

    Google Scholar 

  • Chen L, Xu J, Feng Y, Wang J, Yu Y, Brookes PC (2015) Responses of soil microeukaryotic communities to short-term fumigation-incubation revealed by MiSeq amplicon sequencing. Front Microbiol 6:1149

    Google Scholar 

  • Cheng X, Luo Y, Chen J, Lin G, Chen J, Li B (2006) Short-term C4 plant Spartina alterniflora invasions change the soil carbon in C3 plant-dominated tidal wetlands on a growing estuarine island. Soil Biol Biochem 38:3380–3386

    CAS  Google Scholar 

  • Cheng X, Luo Y, Xu Q, Lin G, Zhang Q, Chen J, Li B (2010) Seasonal variation in CH4 emission and its 13C-isotopic signature from Spartina alterniflora and Scirpus mariqueter soils in an estuarine wetland. Plant Soil 327:85–94

    CAS  Google Scholar 

  • Chomel M, Guittonny-Larchevêque M, Fernandez C, Gallet C, DesRochers A, Paré D, Jackson BG, Baldy V (2016) Plant secondary metabolites: a key driver of litter decomposition and soil nutrient cycling. J Ecol 104:1527–1541

    Google Scholar 

  • Cotrufo MF, Wallenstein MD, Boot CM, Denef K, Paul E (2013) The Microbial Efficiency-Matrix Stabilization (MEMS) framework integrates plant litter decomposition with soil organic matter stabilization: do labile plant inputs form stable soil organic matter? Glob Chang Biol 19:988–995

    Google Scholar 

  • Currin CA, Newell SY, Paerl HW (1995) The role of standing dead Spartina alterniflora and benthic microalgae in salt marsh food webs: considerations based on multiple stable isotope analysis. Mar Ecol-Prog Ser 121:99–116

    Google Scholar 

  • Duan H, Wang L, Zhang Y, Fu X, Tsang YF, Wu J, Le Y (2018) Variable decomposition of two plant litters and their effects on the carbon sequestration ability of wetland soil in the Yangtze River estuary. Geoderma 319:230–238

    CAS  Google Scholar 

  • Duarte CM, Middelburg JJ, Caraco N (2005) Major role of marine vegetation on the oceanic carbon cycle. Biogeosciences 2:1–8

    CAS  Google Scholar 

  • Ertel JR, Hedges JI (1984) The lignin component of humic substances: distribution among soil and sedimentary humic, fulvic, and base-insoluble fractions. Geochim Cosmochim AC 48:2065–2074

    CAS  Google Scholar 

  • Fan F, Li Z, Wakelin SA, Yu W, Liang Y (2012) Mineral fertilizer alters cellulolytic community structure and suppresses soil cellobiohydrolase activity in a long-term fertilization experiment. Soil Biol Biochem 55:70–77

    CAS  Google Scholar 

  • Fernandez I, Cadisch G (2003) Discrimination against 13C during degradation of simple and complex substrates by two white rot fungi. Rapid Commun Mass Spectrom 17:2614–2620

    CAS  Google Scholar 

  • Fukushima M, Yamamoto K, Ootsuka K, Komai T, Aramaki T, Ueda S, Horiya S (2009) Effects of the maturity of wood waste compost on the structural features of humic acids. Bioresour Technol 100:791–797

    CAS  Google Scholar 

  • Goering HK, Van Soest PJ (1970) Forage fiber analysis. Agriculture Handbook No. 379, US Government Printing Office, Washington, DC (USDA-ARS)

  • Graysston SJ, Wang S, Campbell CD, Edwards AC (1998) Selective influence of plant species on microbial diversity in the rhizosphere. Soil Biol Biochem 30:369–378

    Google Scholar 

  • Han SI (2016) Phylogenetic characteristics of bacterial populations and isolation of aromatic compounds utilizing bacteria from humus layer of oak forest. Korean J Microbiol 52:175–182

    Google Scholar 

  • Hu Y, Wang L, Tang Y, Li Y, Chen J, Xi X, Zhang Y, Fu X, Wu J, Sun Y (2014) Variability in soil microbial community and activity between coastal and riparian wetlands in the Yangtze River estuary—potential impacts on carbon sequestration. Soil Biol Biochem 70:221–228

    CAS  Google Scholar 

  • Jex C, Pate G, Blyth A, Spencer R, Hernes P, Khan S, Baker A (2014) Lignin biogeochemistry: from modern processes to quaternary archives. Quat Sci Rev 87:46–59

    Google Scholar 

  • José Luis M-M, María EH, Patricia M-C (2014) Comparing soil carbon sequestration in coastal freshwater wetlands with various geomorphic features and plant communities in Veracruz, Mexico. Plant Soil 378:189–203

    Google Scholar 

  • Kelleher BP, Simpson AJ (2006) Humic substances in soils: are they really chemically distinct? Environ Sci Technol 40:4605–4611

    CAS  Google Scholar 

  • Kutsch WL, Bahn M, Heinemeyer A (2010) Soil carbon dynamics. Cambridge University Press, New York

    Google Scholar 

  • Lehmann J, Kleber M (2015) The contentious nature of soil organic matter. Nature 528:60–68

    CAS  Google Scholar 

  • Lehmann J, Solomon D, Kinyangi J, Dathe L, Wirick S, Jacobsen C (2008) Spatial complexity of soil organic matter forms at nanometre scales. Nat Geosci 1:238–242

    CAS  Google Scholar 

  • Li X, Liu JP, Tian B (2016) Evolution of the Jiuduansha wetland and the impact of navigation works in the Yangtze estuary, China. Geomorphology 253:328–339

    Google Scholar 

  • Li X, Rui J, Mao Y, Yannarell A, Mackie R (2014) Dynamics of the bacterial community structure in the rhizosphere of a maize cultivar. Soil Biol Biochem 68:392–401

    CAS  Google Scholar 

  • Li Y, Chen N, Harmon ME, Li Y, Cao X, Chappell MA, Mao J (2015) Plant species rather than climate greatly alters the temporal pattern of litter chemical composition during long-term decomposition. Sci Rep 5:15783

    CAS  Google Scholar 

  • Liao C, Luo Y, Jiang L, Zhou X, Wu X, Fang C, Chen J, Li B (2007) Invasion of Spartina alterniflora enhanced ecosystem carbon and nitrogen stocks in the Yangtze estuary, China. Ecosystems 10:1351–1361

    CAS  Google Scholar 

  • Liao C, Peng R, Luo Y, Zhou X, Wu X, Fang C, Chen J, Li B (2008) Altered ecosystem carbon and nitrogen cycles by plant invasion: a meta-analysis. New Phytol 177:706–714

    CAS  Google Scholar 

  • Loya WM, Johnson LC, Nadelhoffer KJ (2004) Seasonal dynamics of leaf- and root-derived C in arctic tundra mesocosms. Soil Biol Biochem 36:655–666

    CAS  Google Scholar 

  • Lundell TK, Mäkelä MR, de Vries RP, Hildén KS (2014) Chapter eleven—genomics, lifestyles and future prospects of wood-decay and litter-decomposing basidiomycota. Adv Bot Res 70:329–370

    Google Scholar 

  • Lundell TK, Mäkelä MR, Hildén K (2010) Lignin-modifying enzymes in filamentous basidiomycetes—ecological, functional and phylogenetic review. J Basic Microbiol 50:5–20

    CAS  Google Scholar 

  • Mazzilli S, Kemanian A, Ernst O, Jackson R, Pineiro G (2015) Greater humification of belowground than aboveground biomass carbon into particulate soil organic matter in no-till corn and soybean crops. Soil Biol Biochem 85:22–30

    CAS  Google Scholar 

  • Mendes R, Kruijt M, de Bruijn I, Dekkers E, van der Voort M, Schneider JHM, Piceno YM, DeSantis TZ, Andersen GL, Bakker PAHM, Raaijmakers JM (2011) Deciphering the rhizosphere microbiome for disease-suppressive bacteria. Science 332:1097–1100

    CAS  Google Scholar 

  • Millard P, Midwood AJ, Hunt JE, Whitehead D, Boutton TW (2008) Partitioning soil surface CO2 efflux into autotrophic and heterotrophic components, using natural gradients in soil δ13C in an undisturbed savannah soil. Soil Biol Biochem 40:1575–1582

    CAS  Google Scholar 

  • Moorhead DL, Sinsabaugh RL (2006) A theoretical model of litter decay and microbial interaction. Ecol Monogr 76:151–174

    Google Scholar 

  • Orellana R, Chaput G, Markillie LM, Mitchell H, Gaffrey M, Orr G, DeAngelis KM (2017) Multi-time series RNA-seq analysis of Enterobacter lignolyticus SCF1 during growth in lignin-amended medium. PLoS One 12:e0186440

    Google Scholar 

  • Paul EA (2016) The nature and dynamics of soil organic matter: plant inputs, microbial transformations, and organic matter stabilization. Soil Biol Biochem 98:109–126

    CAS  Google Scholar 

  • Peršoh D (2015) Plant-associated fungal communities in the light of meta’omics. Fungal Divers 75:1–25

    Google Scholar 

  • Phillips DL, Gregg JW (2001) Uncertainty in source partitioning using stable isotopes. Oecologia 127:171–179

    Google Scholar 

  • Quintino V, Sangiorgio F, Ricardo F, Mamede R, Pires A, Freitas R, Rodrigues AM, Basset A (2009) In situ experimental study of reed leaf decomposition along a full salinity gradient. Estuar Coast Shelf Sci 85:497–506

    CAS  Google Scholar 

  • Ravit B, Ehrenfeld JG, Haggblom MM (2003) A comparison of sediment microbial communities associated with Phragmites australis and Spartina alterniflora in two brackish wetlands of New Jersey. Estuar Coasts 26:465–474

    Google Scholar 

  • Šárka A, Tomáš C, Gerrit A, Hana Š, Jiří B, Jan F (2017) Retention of dead standing plant biomass (marcescence) increases subsequent litter decomposition in the soil organic layer. Plant Soil 418:571–579

    Google Scholar 

  • Schmidt MW, Torn MS, Abiven S, Dittmar T, Guggenberger G, Janssens IA, Kleber M, Kogel-Knabner I, Lehmann J, Manning DA, Nannipieri P, Rasse DP, Weiner S, Trumbore SE (2011) Persistence of soil organic matter as an ecosystem property. Nature 478:49–56

    CAS  Google Scholar 

  • Semenov AV, Pereira e Silva MC, Szturc-Koestsier AE, Schmitt H, Falcão Salles J, van Elsas JD (2012) Impact of incorporated fresh 13C potato tissues on the bacterial and fungal community composition of soil. Soil Biol Biochem 49:88–95

    CAS  Google Scholar 

  • Sinsabaugh RL (2010) Phenol oxidase, peroxidase and organic matter dynamics of soil. Soil Biol Biochem 42:391–404

    CAS  Google Scholar 

  • Sinsabaugh RL, Carreiro MM, Repert DA (2002) Allocation of extracellular enzymatic activity in relation to litter composition, N deposition, and mass loss. Biogeochemistry 60:1–24

    CAS  Google Scholar 

  • Šnajdr J, Cajthaml T, Valášková V, Merhautová V, Petránková M, Spetz P, Leppänen K, Baldrian P (2011) Transformation of Quercus petraea litter: successive changes in litter chemistry are reflected in differential enzyme activity and changes in the microbial community composition. FEMS Microbiol Ecology 75:291–303

    Google Scholar 

  • Strope PK, Nickerson KW, Harris SD, Moriyama EN (2011) Molecular evolution of urea amidolyase and urea carboxylase in fungi. BMC Evol Biol 11:1–15

    Google Scholar 

  • Sun J, Steindler L, Thrash JC, Halsey KH, Smith DP, Carter AE, Landry ZC, Giovannoni SJ (2011) One carbon metabolism in SAR11 pelagic marine bacteria. PLoS One 6:e23973. https://doi.org/10.1371/journal.pone.0023973

    Article  CAS  Google Scholar 

  • Tang YS, Wang L, Jia JW, Fu XH, Le YQ, Xz C, Sun Y (2011) Response of soil microbial community in Jiuduansha wetland to different successional stages and its implications for soil microbial respiration and carbon turnover. Soil Biol Biochem 43:638–646

    CAS  Google Scholar 

  • Vandenkoornhuyse P, Baldauf SL, Leyval C, Straczek J, Young JPW (2002) Extensive fungal diversity in plant roots. Science 295:2051

    Google Scholar 

  • Vida C, Bonilla N, de Vicente A, Cazorla FM (2016) Microbial profiling of a suppressiveness-induced agricultural soil amended with composted almond shells. Front Microbiol 7:1–14

    Google Scholar 

  • Waldrop MP, Firestone MK (2004) Microbial community utilization of recalcitrant and simple carbon compounds: impact of oak-woodland plant communities. Oecologia 138:275–284

    Google Scholar 

  • Wang M, Wang Q, Sha C, Chen J (2018) Spartina alterniflorainvasion affects soil carbon in a C3 plant-dominated tidal marsh. Sci Rep 8(628). https://doi.org/10.1038/s41598-017-19111-1

  • Woo HL, Utturkar S, Klingeman D, Simmons BA, DeAngelis KM, Brown SD, Hazen TC (2014) Draft genome sequence of the lignin-degrading Burkholderia sp. strain LIG30, isolated from wet tropical forest soil. Genome Announc 2:e00637–e00614. https://doi.org/10.1128/genomeA.00637-14

    Article  Google Scholar 

  • Xia Y, Wang Y, Wang Y, Chin FY, Zhang T (2016) Cellular adhesiveness and cellulolytic capacity in Anaerolineae revealed by omics-based genome interpretation. Biotechnol Biofuels 9:111

    Google Scholar 

  • Yan J, Wang L, Hu Y, Tsang YF, Zhang Y, Wu J, Fu X, Sun Y (2018) Plant litter composition selects different soil microbial structures and in turn drives different litter decomposition pattern and soil carbon sequestration capability. Geoderma 319:194–203

    CAS  Google Scholar 

  • Yang W, An S, Zhao H, Xu L, Qiao Y, Cheng X (2016) Impacts of Spartina alterniflora invasion on soil organic carbon and nitrogen pools sizes, stability, and turnover in a coastal salt marsh of eastern China. Ecol Eng 86:174–182

    Google Scholar 

  • Zhang WW, Lu ZT, Yang K, Zhu JJ (2017) Impacts of conversion from secondary forests to larch plantations on the structure and function of microbial communities. Appl Soil Ecol 111:73–83

    Google Scholar 

Download references

Acknowledgments

We thanked the International Science Editing for editing the paper.

Funding

This work was supported by the National Natural Science Foundation of China (no. 21876127); National Key Research and Development Project of China (no. 2017YFC0506004); Research Grants Council of the Hong Kong SAR, China (nos. 28300015 and 18202116); the Internal Research Grant (RG 34/2017-2018R and RG 50/2017-2018R) of The Education University of Hong Kong; Science and Technology Developmental Fund Project of Pudong District (no. PKJ2015-C11); and Research Projects of City Environmental Protection Bureau of Pudong District (no. 2016012).

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Lei Wang or Yiu Fai Tsang.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Responsible editor: Zucong Cai

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

ESM 1

(DOCX 219 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yan, J., Wang, L., Tsang, Y.F. et al. Conversion of organic carbon from decayed native and invasive plant litter in Jiuduansha wetland and its implications for SOC formation and sequestration. J Soils Sediments 20, 675–689 (2020). https://doi.org/10.1007/s11368-019-02464-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11368-019-02464-7

Keywords

Navigation