Abstract
Aims
Rising atmospheric CO2 concentrations and nitrogen (N) deposition alter litter decomposition processes that control soil carbon (C) and nutrient cycles. However, few studies have explored such impacts on litter decomposition and micronutrient and macronutrient (C, N, phosphorus (P), potassium (K), calcium (Ca), and magnesium (Mg)) release in a heavy-metal-contaminated environment.
Methods
We performed an open-top chamber experiment to explore the effects of 15-month elevated CO2 and N addition on leaf litter decomposition rate and nutrient release of Cinnamomum camphora (non-N-fixing species) and Acacia auriculiformis (N-fixing species) during litter decomposition in cadmium (Cd)-contaminated environment.
Results
We found that Cd addition consistently reduced leaf litter nutrient (C, N, P, K, Ca, and Mg) loss, while these negative effects were offset by elevated CO2 (average 10.6%) and N addition (average 23.9%). The mitigative effects of elevated CO2 and N addition together (β = −0.78) far exceeded the effects of each (β = −0.15 for elevated CO2 and β = −0.42 for N addition) separately. Such mitigative effects were related to higher litter quality (the increased N, P and Ca in the initial litter), and higher soil microbial activities (higher ligninase and cellulase activities). Additionally, these mitigative effects on leaf litter nutrient release were greater in C. camphora litter than in A. auriculiformis litter, due to its higher C:N and cellulose: N ratios.
Conclusions
Our results suggest that N addition and elevated CO2 concentration may diminish the negative effects of Cd addition on leaf litter decomposition and increase nutrient cycle, especially in non-N fixing trees under the global change.
Similar content being viewed by others
References
Adair EC, Reich PB, Hobbie SE, Knops JMH (2009) Interactive effects of time, CO2, N and diversity on total belowground carbon allocation and ecosystem carbon storage in a grassland community. Ecosystems 12:1037–1052
Allison SD, Vitousek PM (2005) Responses of extracellular enzymes to simple and complex nutrient inputs. Soil Biol Biochem 37:937–944
Alster CJ, German Donovan P, Ying L, Allison Steven D (2013) Microbial enzymatic responses to drought and to nitrogen addition in a southern California grassland. Soil Biol Biochem 64:68–79
Andersson M, Kjøller A, Struwe S (2004) Microbial enzyme activities in leaf litter, humus and mineral soil layers of European forests. Soil Biol Biochem 36:1527–1537
Bremner JM, Mulvaney CS (1982) Nitrogen-total. In: Page AL, Miller RH, Keeney DR (eds) Methods of soil analysis, part 2: chemical and microbial properties, agronomy monograph 9. Agronomy Society of America, Madison, pp 595–624
Cenini VL, Fornara DA, McMullan G et al (2016) Linkages between extracellular enzyme activities and the carbon and nitrogen content of grassland soils. Soil Biol Biochem 96:198–206
Chen YP, Liu Q, Liu YJ, Jia FA, He XH (2014) Responses of soil microbial activity to cadmium pollution and elevated CO2. Sci Rep 4:4287
Cleveland CC, Reed SC, Keller AB, Nemergut DR, O’Neill SP, Ostertag R, Vitousek PM (2014) Litter quality versus soil microbial community controls over decomposition: a quantitative analysis. Oecologia 174:283–294
Cotrufo MF, Raschi A, Lanini M, Ineson P (1999) Decomposition and nutrient dynamic of Quercus pubescens leaf litter in a naturally enriched CO2 Mediterranean ecosystem. Ecology 13:343–351
Duan QN, Lee JC, Liu YS, Chen H, Hu HY (2016) Distribution of heavy metal pollution in surface soil samples in China: a graphical review. Bull Environ Contam Toxicol 97:303–309
Ferreira V, Koricheva J, Duarte S, Niyogi DK, Guerold F (2016) Effects of anthropogenic heavy metal contamination on litter decomposition in streams- a meta-analysis. Environ Pollut 210:261–270
Freeman C, Liska G, Ostle NJ, Jones SE, Lock MA (1995) The use of fluorogenic substrates for measuring enzyme activity in peatlands. Plant Soil 175:147–152
Gallo M, Amonette R, Lauber C, Sinsabaugh R, Zak D (2004) Microbial community structure and oxidative enzyme activity in nitrogen-amended north temperate forest soils. Microb Ecol 48:218–229
Galloway JN, Townsend AR, Erisman JW et al (2008) Transformation of the nitrogen cycle: recent trends, questions, and potential solutions. Science 320:889–892
Ge XM, Wu L, Tang LZ (2013) Review on research progress of relationships between enzyme and litter decomposition. World For Res 26(1):43–48
He ZM, Yu ZP, Huang ZQ et al (2016) Litter decomposition, residue chemistry and microbial community structure under two subtropical forest plantations: a reciprocal litter transplant study. Appl Soil Ecol 101:84–92
Hobbie SE, Eddy WC, Buyarski CR, Adair EC, Ogdahl ML, Weisenhorn P (2012) Response of decomposing litter and its microbial community to multiple forms of nitrogen enrichment. Ecol Monogr 82:389–405
Hou EQ, Xiang HM, Li JL, Li J, Wen DZ (2014) Heavy metal contamination in soils of remnant natural and plantation forests in an urbanized region of the Pearl River Delta, China. Forests 5(5):885–900
IPCC (2019) IPCC special report on the ocean and cryosphere in a changing climate
Koopmans CJ, Tietema A, Verstraten JM (1998) Effects of reduced N deposition on litter decomposition and N cycling in two N saturated forests in the Netherlands. Soil Biol Biochem 30:141–151
Li J, Fang YT, Yoh M, Wang XM, Wu ZY, Kuang YW, Wen DZ (2012) Organic nitrogen deposition in precipitation in metropolitan Guangzhou city of southern China. Atmos Res 113:57–67
Liu GS, Jiang NH, Zhang LD (1996) Soil physical and chemical analysis & description of soil profiles. Standards Press of China, Beijing
Liu JX, Fang X, Deng Q, Han TF, Huang WJ, Li YY (2015) CO2 enrichment and N addition increase nutrient loss from decomposing leaf litter in subtropical model forest ecosystems. Sci Rep 5:7952
Lü YN, Wang CY, Wang FY, Zhao GY, Pu GZ, Ma X, Tian XJ (2013) Effects of nitrogen addition on litter decomposition, soil microbial biomass, and enzyme activities between leguminous and non-leguminous forests. Ecol Res 28:793–800
Luo XZ, Hou EQ, Zang XW, Zhang LL, Yi YF, Wen DZ (2019a) Effects of elevated atmospheric CO2 and nitrogen deposition on leaf litter and soil carbon degrading enzyme activities in a cd-contaminated environment: a mesocosm study. Sci Total Environ 671:157–164
Luo XZ, Hou EQ, Zhang LL, Zang XW, Yi YF, Zhang GH, Wen DZ (2019b) Effects of forest conversion on carbon-degrading enzyme activities in subtropical China. Sci Total Environ 696:133968
Mo JM, Brown S, Xue JH, Fang YT, Li ZA (2006) Response of litter decomposition to simulated N deposition in disturbed, rehabilitated and mature forests in subtropical China. Plant Soil 282:135–151
Nelson DW, Sommers L (1982) Total carbon, organic carbon, and organic matter. Methods of Soil Analysis, Part 2. Chemical and Microbial Properties. Agronomy Society of America, Agronomy Monograph 9, Madison, pp. 539-552
Ochoa-Hueso R, Delgado-Baquerizo M, An King PT, 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
Olson JS (1963) Energy storage and the balance of producers and decomposition in ecological system. Ecology 44:322–331
Pancotto VA, Sala OE, Cabello M, Lopez M, Robson TM, Ballare C, Caldwell MM, Scopel A (2003) Solar UV-B decreases decomposition in herbaceous plant litter in Tierra del Fuego, Argentina: potential role of an altered decomposer community. Glob Change Biol 9(10):1465–1474
Parton W, Silver WL, Burke IC, Grassens L, Harmon ME, Currie WS, King JY, Adair EC, Brandt LA, Hart SC, Fasth B (2007) Global-scale similarities in nitrogen release patterns during long-term decomposition. Science 315:361–364
Ren R, Mi F, Bai N (2000) A chemometrics analysis on the data of precipitation chemistry of China. J Beijing Polytech Univ 26:90–95
Rowland AP, Roberts JD (1994) Lignin and cellulose fractionation in decomposition studies using acid-detergent fibre methods. Commun Soil Sci Plan 25:269–277
Shen GQ, Cao LK, Lu YT, Hong JB (2005) Influence of phenanthrene on cadmium toxicity to soil enzymes and microbial growth. Environ Sci Pollut R 12:259–263
Siegenthaler A, Buttler A, Bragazza L, van der Heijden E, Grosvernier P, Gobat JM, Mithchell EAD (2010) Litter- and ecosystem-driven decomposition under elevated CO2 and enhanced N deposition in a Sphagnum peatland. Soil Biol Biochem 42:968–977
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
Song XZ, Zhou GM, Gu HH, Qi LH (2015) Management practices amplify the effects of N deposition on leaf litter decomposition of the Moso bamboo forest. Plant Soil 395:391–400
Sun FF, Kuang YW, Wen DZ et al (2010) Long-term tree growth rate, water use efficiency, and tree ring nitrogen isotope composition of Pinus massoniana L. in response to global climate change and local nitrogen deposition in southern China. J Soils Sediments 10:1453–1465
Vance ED, Brookes PC, Jenkinson DS (1987) An extraction method for measuring soil microbial biomass C. Soil Biol Biochem 19:703–707
Waring BG (2012) A meta-analysis of climatic and chemical controls on leaf litter decay rates in tropical forests. Ecosystems 15:999–1009
Xia MX, Talhelm AF, Pregitzer KS (2017) Chronic nitrogen deposition influences the chemical dynamics of leaf litter and fine roots during decomposition. Soil Biol Biochem 112:24–34
Xue YT, Lin YH, He XB, Luo YL, Wu X, Xiao JM, Chen T (2018) Effects of lead on the decomposition of Phyllostachys pubescens leaf litter in western Hu’nan province. J Chongqing Norm Univ 35(1):117–124
Zang XW, Luo XZ, Hou EQ et al (2022) Effects of elevated CO2 concentration and nitrogen addition on the chemical compositions, construction cost, and payback time of subtropical trees in Cd-contaminated mesocosm soil. Tree Physiol 42(5):1002–1015
Zheng ZM, Mamuti M, Liu HM, Shu YB, Hu SJ, Wang XH, Li BB, Lin L, Li X (2017) Effects of nutrient additions on litter decomposition regulated by phosphorus-induced changes in litter chemistry in a subtropical forest, China. Forest Ecol Manag 400(15):123–128
Zhou GX, Zhang JB, Qiu XW, Wei F, Xu XF (2018) Decomposing litter and associated microbial activity responses to nitrogen deposition in two subtropical forests containing nitrogen-fixing or non-nitrogen-fixing tree species. Sci Rep-UK 8:12934
Acknowledgements
This research was funded by the National Natural Science Foundation of China (31570483, 31870464, 32201406), and Guangdong Basic and Applied Basic Research Foundation (2021A1515110837).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors have no conflict of interest to declare.
Additional information
Responsible Editor: Alfonso Escudero.
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
ESM 1
(DOC 1427 kb)
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
Luo, X., Zhang, L., Yi, Y. et al. Elevated CO2 and nitrogen addition diminish the inhibitory effects of cadmium on leaf litter decomposition and nutrient release. Plant Soil 487, 311–324 (2023). https://doi.org/10.1007/s11104-023-05928-5
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11104-023-05928-5