Abstract
Background and aims
Decomposition of leaf and root litter contributes large amounts of phosphorus (P) to soil and is strongly determined by litter quality, morphology, and microbial activity, but the individual and interactive roles of these factors remain underexplored.
Methods
To fill this gap, field litter decomposition experiment was conducted by collecting leaf and fine root litters (< 2 mm) of crop (from cropland), shrub (from shrubland) and wood (from woodland) and placing the litters into woodland soil for 2 years in subtropical China, in order to evaluate effects of the above factors on leaf and fine root litter P loss of three species among different decomposition stages.
Results
Leaf litter P loss was positively correlated with root P loss, and both were primarily controlled by microbes. Leaf litter P loss was more affected by litter quality, while root litter P loss was more affected by morphology during whole decomposition. However, morphology and litter quality were also important controls of leaf P loss at mid-to-late stages and of root P loss at early-to-mid stages.
Conclusion
Our results highlighted that microbes exerted dominant controls with different importance of litter morphology and litter quality during different decomposition, which weakened the coordination between leaf and root decomposition. Overall, different regulation processes of leaf and root litter P loss and associated drivers at different decomposition stages provided novel insight into accurately predicting litter decomposition related to nutrient cycling under future afforestation.
Similar content being viewed by others
Data availability
The data that support the findings of this study are available on request from the corresponding author.
Abbreviations
- P:
-
Phosphorus
- C:
-
Carbon
- SOC:
-
Soil organic C
- N:
-
Nitrogen
- SLA:
-
Specific leaf area
- SRL:
-
Specific root length
- RTD:
-
Root tissue density
- G+ :
-
Gram-positive bacteria
- G− :
-
Gram-negative bacteria
- F:
-
Fungi
- ACT:
-
Actinomycetes
- SEM:
-
Structural equation modeling
References
Allison SD, Lu Y, Weihe C, Goulden ML, Martiny AC, Treseder KK, Martiny JB (2013) Microbial abundance and composition influence litter decomposition response to environmental change. Ecology 94(3):714–725. https://doi.org/10.1890/12-1243.1
Berg B, Johansson MB, Meentemeyer V (2000) Litter decomposition in a transect of Norway spruce forests: substrate quality and climate control. Can J For Res 30(7):1136–1147. https://doi.org/10.1139/x00-044
Berg B, McClaugherty C (2008) Decomposition, humus formation, carbon sequestration. Plant litter, 2nd edn. Springer-Verlag, Berlin, Heidelberg
Bhatnagar JM, Peay KG, Treseder KK (2018) Litter chemistry influences decomposition through activity of specific microbial functional guilds. Ecol Monogr 88(3):429–444. https://doi.org/10.1002/ecm.1303
Bradford MA, Berg B, Maynard DS, Wieder WR, Wood SA (2016) Understanding the dominant controls on litter decomposition. J Ecol 104(1):229–238. https://doi.org/10.1111/1365-2745.12507
Chen D, Zheng S, Shan Y, Taube F, Bai Y (2013) Vertebrate herbivore-induced changes in plants and soils: linkages to ecosystem functioning in a semi-arid steppe. Funct Ecol 27(1):273–281. https://doi.org/10.1111/1365-2435.12027
Cheng XL, Yang YH, Li M, Dou XL, Zhang QF (2013) The impact of agricultural land use changes on soil organic carbon dynamics in the Danjiangkou Reservoir area of China. Plant Soil 366(1):415–424. https://doi.org/10.1007/s11104-012-1446-6
Collins SL, Micheli F, Hartt L (2000) A method to determine rates and patterns of variability in ecological communities. Oikos 91(2):285–293. https://doi.org/10.1034/j.1600-0706.2000.910209.x
Cotrufo MF, Soong JL, Horton AJ, Campbell EE, Haddix ML, Wall DH, Parton WJ (2015) Formation of soil organic matter via biochemical and physical pathways of litter mass loss. Nat Geosci 8(10):776–779. https://doi.org/10.1038/ngeo2520
Elser JJ (2012) Phosphorus: a limiting nutrient for humanity? Curr Opin Biotechnol 23(6):833–838. https://doi.org/10.1016/j.copbio.2012.03.001
Elser JJ, Bracken ME, Cleland EE, Gruner DS, Harpole WS, Hillebrand H, Ngai JT, Seabloom EW, Shurin JB, Smith JE (2007) Global analysis of nitrogen and phosphorus limitation of primary producers in freshwater, marine and terrestrial ecosystems. Ecol Lett 10(12):1135–1142. https://doi.org/10.1111/j.1461-0248.2007.01113.x
Esperschütz J, Zimmermann C, Dümig A, Welzl G, Buegger F, Elmer M, Munch JC, Schloter M (2013) Dynamics of microbial communities during decomposition of litter from pioneering plants in initial soil ecosystems. Biogeosciences 10(7):5115–5124. https://doi.org/10.5194/bg-10-5115-2013
Fujii S, Makita N, Mori AS, Takeda H (2016) A stronger coordination of litter decomposability between leaves and fine roots for woody species in a warmer region. Trees 30:395–404. https://doi.org/10.1007/s00468-015-1221-4
Fujii S, Takeda H (2010) Dominant effects of litter substrate quality on the difference between leaf and root decomposition process above-and belowground. Soil Biol Biochem 42(12):2224–2230. https://doi.org/10.1016/j.soilbio.2010.08.022
García-Palacios P, McKie BG, Handa IT, Frainer A, Hättenschwiler S (2016a) The importance of litter traits and decomposers for litter decomposition: a comparison of aquatic and terrestrial ecosystems within and across biomes. Funct Ecol 30(5):819–829
García-Palacios P, Shaw EA, Wall DH, Hättenschwiler S (2016b) Temporal dynamics of biotic and abiotic drivers of litter decomposition. Ecol Lett 19(5):554–563. https://doi.org/10.1111/1365-2435.12589
Ge JL, Ma BY, Xu WT, Zhao CM, Xie ZQ (2022) Temporal shifts in the relative importance of climate and leaf litter traits in driving litter decomposition dynamics in a chinese transitional mixed forest. Plant Soil 1–14. https://doi.org/10.1007/s11104-022-05425-1
Gessner MO, Swan CM, Dang CK, McKie BG, Bardgett RD, Wall DH, Hättenschwiler S (2010) Diversity meets decomposition. Trends Ecol Evol 25(6):372–380. https://doi.org/10.1016/j.tree.2010.01.010
Grace JB (2006) Structural equation modeling and natural systems. Cambridge University Press, Cambridge
Guo L, Deng M, Yang S, Liu W, Wang X, Wang J, Liu L (2021) The coordination between leaf and fine root litter decomposition and the difference in their controlling factors. Glob Ecol Biogeogr 30(11):2286–2296. https://doi.org/10.1111/geb.13384
Harpole WS, Ngai JT, Cleland EE, Seabloom EW, Borer ET, Bracken ME, Elser JJ, Gruner DS, Hillebrand H, Shurin JB, Smith JE (2011) Nutrient co-limitation of primary producer communities. Ecol Lett 14(9):852–862. https://doi.org/10.1111/j.1461-0248.2011.01651.x
Hättenschwiler S, Tiunov AV, Scheu S (2005) Biodiversity and litter decomposition in terrestrial ecosystems. Annu Rev Ecol Evol Syst 36:191–218. https://doi.org/10.1146/annurev.ecolsys.36.112904.151932
Helfrich M, Ludwig B, Thoms C, Gleixner G, Flessa H (2015) The role of soil fungi and bacteria in plant litter decomposition and macroaggregate formation determined using phospholipid fatty acids. Appl Soil Ecol 96:261–264. https://doi.org/10.1016/j.apsoil.2015.08.023
Hobbie SE, Oleksyn J, Eissenstat DM, Reich PB (2010) Fine root decomposition rates do not mirror those of leaf litter among temperate tree species. Oecologia 162:505–513. https://doi.org/10.1007/s00442-009-1479-6
Horodecki P, Nowiński M, Jagodziński AM (2019) Advantages of mixed tree stands in restoration of upper soil layers on postmining sites: a five-year leaf litter decomposition experiment. Land Degrad Dev 30(1):3–13. https://doi.org/10.1002/ldr.3194
Hu Z, Xu C, McDowell NG, Johnson DJ, Wang M, Luo Y, Zhou X, Huang Z (2017) Linking microbial community composition to C loss rates during wood decomposition. Soil Biol Biochem 104:108–116. https://doi.org/10.1016/j.soilbio.2016.10.017
Johansson JF, Paul LR, Finlay RD (2004) Microbial interactions in the mycorrhizosphere and their significance for sustainable agriculture. FEMS Microbiol Ecol 48(1):1–13. https://doi.org/10.1016/j.femsec.2003.11.012
Kaiser C, Franklin O, Dieckmann U, Richter A (2014) Microbial community dynamics alleviate stoichiometric constraints during litter decay. Ecol Lett 17(6):680–690. https://doi.org/10.1111/ele.12269
Liao C, Long CY, Zhang Q, Cheng XL (2022) Stronger effect of litter quality than microorganisms on leaf and root litter C and N loss at different decomposition stages following a subtropical land use change. Funct Ecol. Accepted Author Manuscript. https://doi.org/10.1111/1365-2435.13999
Lin D, Yang S, Dou P, Wang H, Wang F, Qian S, Yang G, Zhao L, Yang Y, Fanin N (2020) A plant economics spectrum of litter decomposition among coexisting fern species in a sub-tropical forest. Ann Bot 125(1):145–155. https://doi.org/10.1093/aob/mcz166
Luo D, Cheng R, Shi Z, Wang W (2017) Decomposition of leaves and fine roots in three subtropical plantations in China affected by litter substrate quality and soil microbial community. Forests 8(11):412. https://doi.org/10.3390/f8110412
Luo M, Moorhead DL, Ochoa-Hueso R, Mueller CW, Ying SC, Chen J (2022) Nitrogen loading enhances phosphorus limitation in terrestrial ecosystems with implications for soil carbon cycling. Funct Ecol 36:2845–2858. https://doi.org/10.1111/1365-2435.14178
Makita N, Kawamura A, Osawa A (2015) Size-dependent morphological and chemical property of fine root litter decomposition. Plant Soil 393(1):283–295. https://doi.org/10.1007/s11104-015-2491-8
Moore TR, Trofymow JA, Prescott CE, Fyles J, Titus BD (2006) Patterns of carbon, nitrogen and phosphorus dynamics in decomposing foliar litter in canadian forests. Ecosystems 9(1):46–62. https://doi.org/10.1007/s10021-004-0026-x
Ochoa-Hueso R, Delgado-Baquerizo M, King PTA, Benham M, Arca V, Power SA (2019) Ecosystem type and resource quality are more important than global change drivers in regulating early stages of litter decomposition. Soil Biol Biochem 129:144–152. https://doi.org/10.1016/j.soilbio.2018.11.009
Parsons SA, Congdon RA, Lawler IR (2014) Determinants of the pathways of litter chemical decomposition in a tropical region. New Phytol 203(3):873–882. https://doi.org/10.1111/nph.12852
Peng Y, Yang W, Yue K, Tan B, Huang C, Xu Z, Li X, Zhang L, Wu F (2018) Temporal dynamics of phosphorus during aquatic and terrestrial litter decomposition in an alpine forest. Sci Total Environ 642:832–841. https://doi.org/10.1016/j.scitotenv.2018.06.135
Plaster E (2013) Soil science and management. Cengage Learning
Portillo-Estrada M, Pihlatie M, Korhonen JF, Levula J, Frumau AK, Ibrom A, Jonas J, Lembrechts JJ, Morillas L, Horváth L, Jones SK, Niinemets Ü (2016) Climatic controls on leaf litter decomposition across european forests and grasslands revealed by reciprocal litter transplantation experiments. Biogeosciences 13(5):1621–1633. https://doi.org/10.5194/bg-13-1621-2016
Qu H, Pan C, Zhao X, Lian J, Wang S, Wang X, Ma X, Liu L (2019) Initial lignin content as an indicator for predicting leaf litter decomposition and the mixed effects of two perennial gramineous plants in a desert steppe: a 5-year long‐term study. Land Degrad Dev 30(14):1645–1654. https://doi.org/10.1002/ldr.3343
Schlesinger WH (1977) Carbon balance in terrestrial detritus. Annu Rev Ecol Syst 8(1):51–81. https://doi.org/10.1146/annurev.es.08.110177.000411
See CR, Luke McCormack M, Hobbie SE, Flores-Moreno H, Silver WL, Kennedy PG (2019) Global patterns in fine root decomposition: climate, chemistry, mycorrhizal association and woodiness. Ecol Lett 22(6):946–953. https://doi.org/10.1111/ele.13248
Strickland MS, Osburn E, Lauber C, Fierer N, Bradford MA (2009) Litter quality is in the eye of the beholder: initial decomposition rates as a function of inoculum characteristics. Funct Ecol 23(3):627–636. https://doi.org/10.1111/j.1365-2435.2008.01515.x
Sun T, Hobbie SE, Berg B, Zhang H, Wang Q, Wang Z, Hättenschwiler S (2018) Contrasting dynamics and trait controls in first-order root compared with leaf litter decomposition. Proc Natl Acad Sci USA 115(41):10392–10397. https://doi.org/10.1073/pnas.1716595115
van Chen J, Hungate BA, Terrer C, van Groenigen JW, Maestre FT, Ying SC, Luo YQ, Jorgensen U, Sinsabaugh RL, Olesen JE, Elsgaard L (2020) Long-term nitrogen loading alleviates phosphorus limitation in terrestrial ecosystems. Glob Chang Biol 26:5077–5086. https://doi.org/10.1111/gcb.15218
Van Soest PJ, Robertson JB, Lewis BA (1991) Methods for Dietary Fiber, Neutral Detergent Fiber, and Nonstarch Polysaccharides in Relation to Animal Nutrition. J Dairy Sci 74(10):3583–3597. https://doi.org/10.3168/jds.S0022-0302(91)78551-2
Voříšková J, Baldrian P (2013) Fungal community on decomposing leaf litter undergoes rapid successional changes. ISME J 7(3):477–486. https://doi.org/10.1038/ismej.2012.116
Wardle DA, Barker GM, Bonner KI, Nicholson KS (1998) Can comparative approaches based on plant ecophysiological traits predict the nature of biotic interactions and individual plant species effects in ecosystems? J Ecol 86(3):405–420. https://doi.org/10.1046/j.1365-2745.1998.00268.x
Wen Z, Li H, Shen Q, Tang X, Xiong C, Li H, Pang J, Ryan MH, Lambers H, Shen J (2019) Tradeoffs among root morphology, exudation and mycorrhizal symbioses for phosphorus-acquisition strategies of 16 crop species. New Phytol 223:882–895. https://doi.org/10.1111/nph.15833
Wickings K, Grandy AS, Reed SC, Cleveland CC (2012) The origin of litter chemical complexity during decomposition. Ecol Lett 15(10):1180–1188. https://doi.org/10.1111/j.1461-0248.2012.01837.x
Wilkinson SC, Anderson JM, Scardelis SP, Tisiafouli M, Taylor A, Wolters V (2002) PLFA profiles of microbial communities in decomposing conifer litters subject to moisture stress. Soil Biol Biochem 34(2):189–200. https://doi.org/10.1016/S0038-0717(01)00168-7
Williams M, Schwarz PA, Law BE, Irvine J, Kurpius MR (2005) An improved analysis of forest carbon dynamics using data assimilation. Glob Change Biol 11(1):89–105. https://doi.org/10.1111/j.1365-2486.2004.00891.x
Wu JJ, Zhang Q, Yang F, Lei Y, Zhang QF, Cheng XL (2016) Afforestation impacts microbial biomass and its natural (13)C and (15)N abundance in soil aggregates in central China. Sci Total Environ 568:52–56. https://doi.org/10.1016/j.scitotenv.2016.05.224
Xu X, Hirata E (2005) Decomposition patterns of leaf litter of seven common canopy species in a subtropical forest: N and P dynamics. Plant Soil 273(1):279–289. https://doi.org/10.1007/s11104-004-8069-5
Yue K, García-Palacios P, Parsons SA, Yang W, Peng Y, Tan B, Huang C, Wu F (2018) Assessing the temporal dynamics of aquatic and terrestrial litter decomposition in an alpine forest. Funct Ecol 32(10):2464–2475. https://doi.org/10.1111/1365-2435.13143
Zhang Q (2009) The south-to‐north water transfer project of China: Environmental implications and monitoring strategy 1.JAWRA J Am Water Resour Assoc 45(5):1238–1247. https://doi.org/10.1111/j.1752-1688.2009.00357.x
Zhu J, He X, Wu F, Yang W, Tan B (2012) Decomposition of Abies faxoniana litter varies with freeze–thaw stages and altitudes in subalpine/alpine forests of southwest China. Scand J Forest Res 27(6):586–596. https://doi.org/10.1080/02827581.2012.670726
Zhang Q, Wu J, Yang F, Lei Y, Zhang Q, Cheng X (2016) Alterations in soil microbial community composition and biomass following agricultural land use change. Sci Rep 6(1):1–10. https://doi.org/10.1038/srep36587
Acknowledgements
This research was financially supported by the National Natural Science Foundation of China (32130069) and the “Strategic Priority Research Program A of the Chinese Academy of Sciences” (XDA26010102). We thank Fan Yang, Dandan Zhang and Junjun Wu for assistance in the field and laboratory analyses.
Author information
Authors and Affiliations
Contributions
X.L. C and Q. Z conceived the ideas and designed the methodology; C. L and C.Y. L collected the data; C.Y. L and C. L. analyzed the data; X.L. C and C. L led the writing of the manuscript. All authors contributed critically to the drafts and gave final approval for publication.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Responsible Editor: Michael Luke McCormack.
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Chang Liao and Chunyan Long are joint first authors: These authors contributed equally to this work.
Supplementary information
Below is the link to the electronic supplementary material.
ESM 1
(DOCX 2.00 MB)
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Liao, C., Long, C., Zhang, Q. et al. Different regulation processes of litter phosphorus loss for leaf and root under subtropical afforestation. Plant Soil 486, 455–468 (2023). https://doi.org/10.1007/s11104-023-05884-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11104-023-05884-0