PREDICTING THE DECOMPOSITION RATE, MASS LOSS, AND NUTRIENT RELEASE OF SINGLE AND MIXED LEAF LITTER TYPES USING DECOMPOSITION MODELS IN THE NORTHERN GUINEA SAVANNAH OF NIGERIA

Folasade A. Akinsola, Ishaku Y. Amapu, Eunice Y. Oyinyola, Drame Marieme, Christopher Aboyeji

Abstract


Background: This study presented a non-linear model to biologically describe the decomposition pattern, mass loss and nutrient release of four leaf litter species: Khaya senegalensis (African mahogany), Mangifera indica (Mango), Gmelina arborea (Beechwood), Eucalyptus camaldulensis (River red gum) and a mixture of the leaf litters using the standard litter bag technique. Objective: To explore different mathematical decomposition decay models in evaluating the decomposition rate and the relationship between mass loss and chemical parameters of some selected trees in Nigeria's northern Guinea savannah.  Methodology: The experiment was a Completely Randomized Design with three replications. Fifteen litter bags were randomly placed in the field and retrieved at intervals of 0, 14, 28, 42, 56, 84, and 112 days (16 weeks).  Three non-linear models were used to estimate the decomposition rate of the litter. Pearson correlation analysis was used to determine the relationship between mass loss and chemical composition. Results: Decomposition pattern gradually increased from 7 % up to 78.5 % by week 0 to 16 weeks. The leaf litter of Mangifera indica had the highest mass loss (62.9 %), followed by the litter mixture (44.0 %), Eucalyptus camaldulensis (43.6 %), Gmelina arborea (40.5 %) and Khaya senegalensis (39.3 %). Single exponential model (Adj R2=93.25-98.59%), double exponential model (Adj R2=87.93-98.98%), and three parameters asymptotic negative exponential model (Adj R2=93.82-98.84%), described the decomposition process efficiently. Correlation analysis of mass loss and chemical composition was highly significant (p ≤ 0.05), among all the leaf litter chemical properties, organic carbon, phosphorus, and nitrogen were the restraining factors. Implication: The mass loss was closely linked to the chemical properties of all the litter types. Among these properties, organic carbon and phosphorus were the limiting factors. Conclusion: We conclude that the single-leaf litter of Mangifera indica and Khaya senegalensis were superior in chemical composition, and decomposition than the mixed-leaf litter therefore they have the potential to enhancing soil fertility in the study area.

Keywords


decomposition rate; exponential model; leaf litter; mass loss; soil fertility

Full Text:

PDF

References


Aber, J.D., Melillo, J.M. and McClaugherty, C.A., 1990. Predicting long-term patterns of mass loss, nitrogen dynamics, and soil organic matter formation from initial fine litter chemistry in temperate forest ecosystems. Canadian Journal of Botany; 68, pp. 2201-2208. https://doi.org/10.1139/b90-287

Aerts, R. and Caluwe, H., 1997. Nutritional and plant-mediated controls on leaf litter decomposition of Carex species. Ecology, 78(1), pp. 244-260. https://doi.org/10.2307/2265993

Ahlam, A.M., 2004. Assessment of rate of decomposition and nutrient release from leaf residue of some tree species. M.Sc. Thesis in Desertification and Desert Cultivation, University of Khartoum, Sudan.

Anderson, C., Peterson, M. and Curtin, D., 2017. Base cations, KC and Ca2C, have contrasting effects on soil carbon, nitrogen and denitrification dynamics as pH rises. Soil Biology and Biochemistry, 113, pp. 99-107. https://doi.org/10.2136/vzj2017.08.0155

Asigbaase, M., Dawoe, E., Sjogerstan, S. and Lomax, B.H., 2021. Decompositon and nutrient mineralization of leaf litter in smallholder cocoa agroforest: a comparison of organic and conventional farms in Ghana. Journal of Soil and Sediments, 21, pp. 1010-1023. https://doi.org/10.1007/s11368-020-02871-6

Barrios, E., Valencia, V., Jonsson, M., Brauman, A., Hairiah, K., Mortimer, P.E., and Okubo, S., 2018. Contribution of trees to the conservation of biodiversity and ecosystem services in agricultural landscapes. International Journal of Biodiversity of Science and Ecosystem Service Management, 14, pp.1–16. https://doi.org/10.1080/21513732.2017.1399167

Berg, B., and McClaugherty, C., 2014. Plant Litter. Decomposition, Humus Formation, Carbon Sequestration, 3rd ed. Springer Verlag, Heidelberg, Berlin, pp. 317. https://doi.org/10.1007/978-3-662-05349-2

Berg, B., De Marco, A., Davey, M., Emmett, B., Hobbie, S., Liu, C., McClaugherty, C., Norell, L., Johansson, M.-B., Rutigliano, F., Vesterdal, L. and Virzo De Santo, A., 2010. Limit values for foliar litter decomposition in pine forests. Biogeochemistry, 100, pp. 57-73. https://doi.org/10.1007/s10533-009-9392-4

Berg, B., and Ekbohm, G., 1993. Decomposing needle litter in lodgepole pine (Pinus contorta) and Scots pine (Pinus sylvestris) monocultural systems. Is there a maximum mass loss? Scandinavian Journal of Forest Research, 8, pp. 457-465. https://doi.org/10.1080/02827589309382780.

Berg, B. and Staaf, H., 1981. Leaching, accumulation and release of nitrogen in decomposing forest litter. Ecological Bulletins, 33, pp. 163-78. https://www.jstor.org/stable/45128659

Blanco, R. and Aguilar, A., 2015. Soil erosion and erosion thresholds in an agroforestry system of coffee (Coffea arabica) and mixed shade trees (Inga spp. and Musa spp.) in Northern Nicaragua Agriculture Ecosystems and Environment, 210, pp. 25-35. https://doi.org/10.1016/j.agee.2015.04.032

Bockheim, J.G., Jepsen, E.A., and Heisey, D.M., 1991. Nutrient dynamics in decomposing leaf litter of four tree species on a sandy soil in northwestern Wisconsin. Canadian Journal of Forest Research, 21(6), pp. 803-812. https://doi.org/10.1139/x91-113

Bray, R.H. and Kurtz, L., 1945. Determination of total, organic, and available forms of phosphorus in soils. Soil Science; 59(1), pp. 39-46. https://doi.org/10.1097/00010694-194501000-00006

Bünemann, E.K, Bongiorno, G., Bai, Z., Creamer, R.E., De Deyn, G. and de Goede, R., 2018. Soil quality – a critical review. Soil Biology and Biochemistry, 120, pp. 105–125. https://doi.org/10.1016/j.soilbio.2018.01.030

Castro-Díez P., Fierro-Brunnenmeister N., González-Muñoz, N., and Gallardo, A., 2011. Effects of exotic and native tree leaf litter on soil properties of two contrasting sites in the Iberian Peninsula. Plant and Soil, 350, pp. 179–191. https://doi.org/10.1007/s11104-011-0893-9

Certini, G., Vestgarden, L.S., Forte, C., Tau, T. and Strand, L., 2015. Litter decomposition rate and soil organic matter quality in a patchwork heathland of southern Norway, Soil, 1, pp. 207–216. https://doi.org/10.5194/soil-1-207-2015

Dalal, R.C., 1998. Soil microbial biomass: What do the numbers really mean? Australian Journal of Experimental Agriculture, 38, pp. 649-665. https://doi.org/10.1071/EA97142

Dawoe, E.K., Isaac, M.E. and Quashie-Sam, J., 2010. Litterfall and litter nutrient dynamics under cocoa ecosystems in lowland humid Ghana. Plant and Soil, 330, pp. 55–64.https://doi.org/10.1007/s11104-009-0191-5

Domínguez, A., Bedano, C.J., Becker, A.R., and Arolfo, RV., 2014. Organic farming fosters agro-ecosystem functioning in Argentinian temperate soils: evidence from litter decomposition and soil fauna. Applied Soil and Ecology, 83, pp. 170–176. http://dx.doi.org/10.1016/j.apsoil.2013.11.008

Duan, H., Wang, L., Zhang, Y, Fu, X, Tsang, Y and Wu, J., 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, pp. 230–238. http://doi.org/10.1016/j.geoderma.2017.10.050

Fontes, A.G., Gama-Rodrigues, A.C., Gama-Rodrigues, E.F., Sales, M.V.S., Costa, M.G., and Machado, R.C.R., 2014. Nutrient stocks in litterfall and litter in cocoa agroforests in Brazil. Plant and Soil, 383, pp. 313–335. https://doi.org/10.1007/s11104-014-2175-9

Fox, J. and Weisberg, S., 2011. An R Companion to Applied Regression. Sage, Thousand Oaks, CA, second edition.

Hayashi, S.N., Vieira, I.C.G., Carvalho, C.J.R. and Davidson, E., 2012. Linking nitrogen and phosphorus dynamics in litter production and decomposition during secondary forest succession in the eastern Amazon. Boletim do Museu Paraense Emílio Goeldi. Ciências Naturais, 7, pp.283–295. https://doi.org/10.46357/bcnaturais.v7i3.591

Hothorn, T., Bretz, F. and Westfall, P., 2008. Simultaneous inference in general parametric models. Biometrical Journal: Journal of Mathematical Methods in Biosciences, 50(3), pp. 346-363. https://doi.org/10.1002/bimj.200810425.

Hunt, H.W. 1977. A simulation model for decomposition in grasslands. Ecology, 58, pp. 469-484. https://doi.org/10.2307/1938998

Institute for Agricultural Research Metrological station, IARMS., 2021. Metrological data from IAR metrological station, Ahmadu Bello University, Samaru, Zaria Nigeria.

Kaba, J.S., 2017. Nitrogen nutrition of cocoa (Theobroma cacao L.) in intercropping systems with gliricidia (Gliricidia sepium (Jacq.) Kunth ex Walp.). PhD Thesis of The Free University of Bozen-Bolzano, Faculty of Science and Technology, Bolzano, Italy.

Karberg, N.J., Scott, N.A. and Giardina, C.P., 2008. Methods for Estimating Litter Decomposition Chapter 8. In: C.M. Hoover, ed. Field measurements for forest carbon monitoring: A landscape-scale approach. New York, NY: Springer Science + Business Media: pp. 103-111.

Kumar, B.M., 2008. Litter dynamics in plantation and agroforestry systems of the tropics—a review of observations and methods. In: D.R. Batish, R.K. Kohli, S. Jose and H.P. Singh, eds. Ecological basis of agroforestry, Boca Raton:CRC Press.

Liao, C., Long, C. and Zhang, Q., 2022. Stronger effect of litter quality than micro-organisms on leaf and root litter C and N loss at different decomposition stages following a subtropical land use change. Functional Ecology, 1, pp. 1–12. https://doi.org/10.1111/1365-2435.13999

Lin, H., Li, Y., Bruelheide, H., Zhang, S., Ren, H. and Zhang, N., 2021. What drives leaf litter decomposition and the decomposer community in subtropical forests – the richness of the above-ground tree community or that of the leaf litter? Soil Biological and Biochemistry, 160, pp. 108314. https://doi.org/10.1016/j.soilbio.2021.108314

Lin, D., Pang, M., Fanin, N., Wang, H., Qian, S., Zhao, L., Yang, Y., Mi, X. and Ma, K., 2019. Fungi participate in driving home-field advantage of litter decomposition in a subtropical forest. Plant and Soil, 434, pp. 467–480. https://doi.org/10.1007/s11104-018-3840-7

Liu, P., Huang, J., Sun, O.J. and Han, X., 2010. Litter decomposition and nutrient release as affected by soil nitrogen availability and litter quality in a semiarid grassland ecosystem. Oecologia, 162, pp. 771-780. https://doi.org/10.1007/s00442-009-1513-7

Lori, M., Symnaczik, S., Mäder, P., De Deyn, G. and Gattinger, A., 2017. Organic farming enhances soil microbial abundance and activity meta-analysis and meta-regression. PLoS One, 12(7), pp. 18-44. https://doi.org/10.1371/journal.pone.0180442

Mahmood, V., Siddique, M. R. H. and Abdullah, S. M. R., 2014. Nutrient dynamics associated with leaching and microbial decomposition of four abundant mangrove species leaf litter of the Sundarbans, Bangladesh. Wetlands; 34 (3), pp. 439-448. https://doi.org/10.1007/s13157-013-05

Mohammed, K. O., 2013. Mineralization of neem seed cake and effect on growth and nutrition of sorghum in a northern Guinea Savanna Alfisol. Unpublished Ph.D Thesis, Department of Soil Science, Ahmadu Bello University, Zaria. Pp. 32-35

Mohammed, A.M., Robinson, J.S., Midmore, D.J. and Verhoef, A., 2019. Leaf litter decomposition and mitigation of CO2 emissions in cocoa ecosystems. In: A.M. Mohammed, J.S. Robinson, D.J.. Midmore and A. Verhoef. Eds.CO2 Sequestration, Londo:IntechOpen. pp.20-23. https://doi.org/10.5772/intechopen.86520

Moyer, R.A., Hummer, K.E., Finn, C.E., Frei, B. and Wrolstad, R.E., 2002. Anthocyanins, phenolics, and antioxidant capacity in diverse small fruits: Vaccinium, Rubus, and Ribes. Journal of Agriculture and Food Chemistry, 50 (3), pp. 519–525. https://doi.org/10.1021/jf010625a

Naik, S.K., Maurya, S., Mukherjee, D., Singh, A.K. and Bhatt, B.P., 2018. Rates of decomposition and nutrient mineralization of leaf litter from different orchards under hot and dry sub-humid climate. Archive of Agronomy and Soil Science 64, pp. 560-573. http://doi.org/10.1080/03650340.2017.1362104

Novara, A., Rühl, J., La Mantia, T., Gristina, L., La Bella, S. and Tuttolomondo, T., 2015. Litter contribution to soil organic carbon in the processes of agriculture abandon. Solid Earth, 6, pp. 425–432. https://doi.org/10.5194/se-6-425-2015.

Okalebo, J.R., Gathua, K.W. and Woomer, P.L., 2002. Laboratory methods of soil analysis: A working manual, 2nd ed. Nairobi:TSBR-CIAT and SACRED Africa.

Olson, J.S., 1963. Energy storage and the balance of producers and decomposers in ecological systems. Ecology, 44, pp. 322-331. https://doi.org/10.2307/1932179

Podong, C., Poolsiri, R., Katzensteinern K., Pengthamkeerati, P. and Thongdeenok, P., 2013 Species diversity and litter dynamics in secondary mixed deciduous forest, ThungSalaeng Lung National Park, Northern, Thailand. Folia Forestalia Polonica; 55, pp. 196–204. https://doi.org/10.2478/ffp-2013-0022

Quer, E., Pereira, S., Michael, T., Santonja, M., Gauquelin, T., Simioni, G., Oureival, J.M., Joffre, R., Limousin, J.M. and Aupic-Samain, A., 2022. Amplified Drought Alters Leaf Litter Metabolome, Slows Down Litter Decomposition, and Modifies Home Field (Dis) Advantage in Three Mediterranean Forests. Plants; 11, pp. 25-28. https://doi.org/10.3390/plants11192582

R Core Team., 2018. A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.

Ren, Z., Zhao, H., Fu, Y., Xiao, L., and Dong, Y., 2022. Effects of urban street trees on human thermal comfort and physiological indices: a case study in Changchun city, China. Journal of Forestry Research, 33(3), pp. 911-922. https://doi.org/10.1007/s11676-021-01502-17

Ruwanza, S., Gaertner, M., Esler, K. J. and Richardson, D.M., 2014. Allelopathic effects of invasive Eucalyptus camaldulensis on germination and early growth of four native species in the Western Cape, South Africa. Southern Forests: Journal of Forest Science, 77, pp. 91–105. https://doi.org/10.2989/20702620.2014.965985

Saez-Plaza, Michalowski, T., Navas, M.J. and Asuero, A. G., 2013. An overview of the Kjeldahl method of nitrogen determination part 1. Early history, chemistry of the procedure, and titrimetric finish. Critical Review in Analytical Chemistry, 4, pp. 43-45. https://doi.org/10.1080/10408347.2013.786239

Singh, K., Trivedi, P., Singh, G., Singh, B. and Patra, D. D., 2014. Effect of different leaf litters on carbon, nitrogen and microbial activities of sodic soils. Land Degradation Development, 3, pp. 207-213. https://doi.org/10.1002/ldr.2160.

Singh, K.P., Singh, P.K. and Tripathy, S.K., 1999. Litterfall, litter decomposition and nutrient release patterns in four native tree species raised on coal mine spoil at Singrauli, India. Biology and Fertility of Soils, 29, pp. 371-378. https://doi.org/10.1007/s003740050567

Swift, J.A., Heal, O.W. and Anderson, J.M., 1979. Decomposition in Terrestrial Ecosystems. Oxford:Blackwell Scientific Publications.

Tarfa, B.D., 2001. Effect of some selected indigenous tree foliage on soil fertility and productivity of a savanna soil. Ph. D. Thesis, Department of Soil Science, Faculty of Agriculture, Ahmadu Bello University, Samaru, Zaria; 164pp.

Taylor, B.R., Parkinson, D. and Parsons W.F.J., 1989. Nitrogen and lignin control of hardwood leaf decomposition dynamics. Ecology, 63, pp. 621-626. https://doi.org/10.2307/1938416

Triadiati, S., Tjitrosemito, E., Sundarsono, G., Qayim, I. and Leuschner, C., 2011. Litterfall production and leaf-litter decomposition at natural forest and cacao agroforestry in Central Sulawesi, Indonesia. Asian Journal of Biology Science, 4(2), pp. 21–234.

Vitousek, P.M., Turner, D.R., Parton, W.J. and Sanford R.L., 1994. Litter decomposition on the Mauna Loa environmental matrix, Hawaii: patterns, mechanisms, and models. Ecology, 75, pp. 418-429. https://doi.org/10.2307/1939545

Watson, C., Atkinson, D., Gosling, P., Jackson, L. and Rayns, F., 2002. Managing soil fertility in organic farming systems. Soil Use and Management, 18, pp. 239-247. https://doi.org/10.1111/j.1475-2743.2002.tb00265.x

Weider, R.K., Carrel, J.E., Rapp, J.K. and Kucera, C.L., 1983. Decomposition of tall fescue (Festuca elatior var. arundinacea) and cellulose litter on surface mines and tallgrass Prairie in central Missouri, USA. Journal of Applied Ecology, 12 (1), pp. 45-49. https://doi.org/10.2307/2403394.

Wei, T., and Viliam, S., 2021. R package “corrplot”: visualization of a Correlation Matrix. R package version 0.92. Available at: https://github.com/taiyun/corrplot

Xiao, H., Sheng, M., Wang, L., Guo, C., and Zhang, S., 2022. Effects of short-term n addition on fine root morphological features and nutrient stoichiometric characteristics of Zanthoxylum bungeanum and Medicago sativa seedlings in southwest China karst area. Journal of Soil Science and Plant Nutrition, 22(2), pp. 1805-1817. https://doi.org/10.1007/s42729-022-00513-5

Zhang, H., Huang, Y., An,s., Zeng, Q., Wang, B., Bai, X and Huang, Q., 2023. Decay stages and meteorological factors affect microbial community during leaf litter in situ decomposition. Soil Ecology Letters. 5(3), pp. 220160. https://doi.org/10.1007/s42832-022-0160-4

Zhu, J., Qiaoling, Y. and Changjie, J., 2010. Comparison of soil microbial biomass C, N, and P between natural secondary forests and Larix olgensis plantations under temperate climate. In: World Congress of Soil Science, Soil Solutions for a Changing World. Brisbane, Australia. Pp 23.




URN: http://www.revista.ccba.uady.mx/urn:ISSN:1870-0462-tsaes.v27i3.55769

DOI: http://dx.doi.org/10.56369/tsaes.5576



Copyright (c) 2024 Christopher Aboyeji

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.