Abstract
We investigated under field and laboratory conditions the decomposition and nutrient release from mixed leaf litters of Faidherbia albida (Del) A. Chev. and Vitellaria paradoxa C.F. Gaertn. f. in the south-Sudanese zone of West Africa. Litterbags containing F. albida and V. paradoxa litters in varying proportions were placed on the soil surface and buried in plots receiving the following treatments: no fertilizer (control); nitrogen; phosphorus as Triple Superphosphate (TSP); and phosphorus as rock phosphate from Burkina Faso (BP). At each litterbags collection date, the undecomposed litter from each species was separated, and its remaining mass, nitrogen, phosphorus and potassium contents were determined. F. albida decomposed faster (k-values ranged from 0.060 to 0.171 week−1) than V. paradoxa (k-values ranged from 0.020 to 0.056 week−1) and released more nutrient than V. paradoxa. Mixing litters accelerated the decomposition rate of both F. albida and V. paradoxa litter. Decomposition was faster in the nitrogen and TSP plots than in the control and BP plots, and buried litter decomposed more rapidly than surface litter Also under laboratory conditions, F. albida litter decomposed more rapidly than V. paradoxa litter as the microbial specific growth rate were 0.135 h−1 and 0.069 h−1, respectively. Results indicated that mixing litters of contrasting qualities may be a promising option to regulating decomposition/mineralization rates from organic material.
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References
Alexander M (1985) Introduction to soil microbiology. Wiley, Chichester
Bationo A, Lompo F, Koala S (1998) Research on nutrient flows and balances in west Africa: state-of-the-art. Agric Ecosyst Environ 71:19–35
Bayala J, Mando A, Ouedraogo SJ, Teklehaimanot Z (2003) Managing Parkia biglobosa and Vitellaria paradoxa prunings for crop production and improved soil properties in the sub-sudanian zone of Burkina Faso. Arid Land Res Manag 17:283–296
Bayala J, Mando A, Teklehaimanot Z, Ouedraogo SJ (2005) Nutrient release from decomposing leaf mulches of karite (Vitellaria paradoxa) and nere (Parkia biglobosa) under semi-arid conditions in Burkina Faso, West Africa. Soil Biol Biochem 37:533–539
Berg B (2000) Litter decomposition and organic matter turnover in northern forest soils. For Ecol Manage 133:13–22
Blair JM, Crossley DA, Callaham LC (1992) Effects of litter quality and microarthropods on N dynamics and retention of exogenous 15N in decomposing litter. Biol Fertil Soils 12:241–252
Budelman A (1988) The decomposition of the leaf mulches of Leucaena leucocephala, Gliricidia sepium and Flemingia macrophylla under humid tropical conditions. Agroforest Syst 7:33–45
Constantinides M, Fownes JH (1994) Nitrogen mineralization from leaves and litter of tropical plants: relationship to nitrogen, lignin and soluble polyphenol concentrations. Soil Biol Biochem 26:49–55
Fontès J, Guinko S (1995) Carte de la végétation et de l’occupation du sol du Burkina Faso. Institut de la Carte International de la Végétation. Université Toulouse France; Institut du Développment Rural, Université Ouagadougou, Burkina Faso, 66 pp
Fyles JW, Fyles IH (1993) Interaction of Douglas-fir with red alder and salal foliage litter during decomposition. Can J For Res 23:358–361
Gartner TB, Cardon ZG (2004) Decomposition dynamics in mixed-species leaf litter. Oikos 104:230–246
Hall JB, Aebischer DP, Tomlinson HF, Osei-Amaning E, Hindle JR (1996) Vitellaria paradoxa. A Monograph. School of Agricultural and Forest Sciences, University of Wales Bangor, UK, 105 pp
Ilstedt U, Nordgren A, Malmer A (2000) Optimum soil water for soil respiration before and after amendment with glucose in humid tropical acrisols and a boreal mor layer. Soil Biol Biochem 32:1591–1599
Kaneko N, Salamanca EF (1999) Mixed leaf litter effects on decomposition rates and soil microarthropod communities in an oak-pine stand in Japan. Ecol Res 14:131–138
Kwabiah AB, Voroney RP, Palm CA, Stoskopf NC (1999) Inorganic fertilizer enrichment of soil: effect on decomposition of plant litter under subhumid tropical conditions. Biol Fertil Soils 30:224–231
Liu P, Huang JH, Han XG, Sun OJ, Zhou Z (2006) Differential responses of litter decomposition to increased soil nutrients and water between two contrasting grassland plant species of Inner Mongolia, China. Appl Soil Ecol 34:266–275
Musvoto C, Campbell BM, Kirchmann H (2000) Decomposition and nutrient release from mango and miombo woodland litter in Zimbabwe. Soil Biol Biochem 32:1111–1119
Nelson DW, Sommers LE (1982) Total carbon, organic carbon, and organic matter. In: Page AL, Miller RH, Keeny DR (eds) Methods of soils analysis, Part 2, 2nd edn. American Society of Agronomy and Soil science Society of America: Madison, pp 539–579
Nordgren A (1988) Apparatus for the continuous, long-term monitoring of soil respiration rate in large numbers of samples. Soil Biol Biochem 20:955–957
O’ Connell AM (1994) Decomposition and nutrient content of litter in a fertilized eucalypt forest. Biol Fertil Soils 17:159–166
Olson JS (1963) Energy storage and the balance of producers and decomposers in ecological systems. Ecology 44:322–331
Palm CA, Rowland AP (1997) A minimum dataset for characterization of plant quality for decomposition. In: Cadisch G, Giller KE (eds) Driven by nature: plant litter quality and decomposition. CAB Int, Wallingford, pp 379–392
Palm CA, Sanchez PA (1991) Nitrogen release from the leaves of some tropical legumes as affected by their lignin and polyphenolic contents. Soil Biol Biochem 23:83–88
Paul EA, Clark FE (1996) Soil microbiology and biochemistry. Academic Press, San Diego, 340 pp
Paustian K, Ågren GI, Bosatta E (1996) Modelling litter quality effects on decomposition and soil organic matter dynamics. In: Cadisch G, Giller KE (eds) Driven by nature: plant litter quality and decomposition. CAB International, pp 313–335
Prescott CE, Zabek LM, Kabzems CLSR (2000) Decomposition of broadleaf and needle litter in forests of British Columbia: influences of litter type, forest type, and litter mixtures. Can J For Res 30:1742–1750
Richards BN (1987) The microbiology of terrestrial ecosystems. Longman, Harlow, 399 pp
Salamanca EF, Kaneko N, Katagiri S (1998) Effects of leaf litter mixtures on the decomposition of Quercus serrata and Pinus densiflora using field and laboratory microcosm methods. Ecol Eng 10:53–73
Sall SN, Masse D, Bernhard-Reversat F, Guisse A, Chotte JL (2003) Microbial activities during the early stage of laboratory decomposition of tropical leaf litters: the effect of interactions between litter quality and exogenous inorganic nitrogen. Biol Fertil Soils 39:103–111
Schimel JP, Hattenschwiler S (2007) Nitrogen transfer between decomposing leaves of different N status. Soil Biol Biochem 39:1428–1436
Semwal RL, Maikhuri RK, Rao KS, Sen KK, Saxena KG (2003) Leaf litter decomposition and nutrient release patterns of six multipurpose tree species of central Himalaya, India. Biomass Bioenerg 24:3–11
Teklay T (2007) Decomposition and nutrient release from pruning residues of two indigenous agroforestry species during the wet and dry seasons. Nutr Cycl Agroecosys 77:115–126
Teklay T, Malmer A (2004) Decomposition of leaves from two indigenous trees of contrasting qualities under shaded-coffee and agricultural land-uses during the dry season at Wondo Genet, Ethiopia. Soil Biol Biochem 36:777–786
Teklay T, Nordgren A, Nyberg G, Malmer A (2007) Carbon mineralization of leaves from four Ethiopian agroforestry species under laboratory and field conditions. Appl Soil Ecol 35:193–202
Tilander Y (1996) Competition for and conservation of water and nutrients in agroforestry systems in semi-arid West Africa. Ph.D thesis. Departement of Ecology and Environmental Reaserch. Swedish University of Agricultural Sciences, Uppsala, Sweden, p 378
Vanlauwe B, Sanginga N, Merckx R (1997) Decomposition of four Leucaena and Senna prunings in alley cropping systems under sub-humid tropical conditions: the process and its modifiers. Soil Biol Biochem 29:131–137
Vanlauwe B, Vanlangenhove G, Merckx R, Vlassak K (1995) Impact of rainfall regime on the decomposition of leaf-litter with contrasting quality under subhumid tropical conditions. Biol Fert Soils 20:8–16
Walinga I, van der Lee JJ, Houba VJG, van Vark W, Novozamsky I (1995) Plant analysis manual. Kluwer Academic, Dordrecht, 272 pp
Wardle DA, Bonner KI, Nicholson KS (1997) Biodiversity and plant litter: experimental evidence which does not support the view that enhanced species richness improves ecosystem function. Oikos 79:247–258
Wedderburn ME, Carter J (1999) Litter decomposition by four functional tree types for use in silvopastoral systems. Soil Biol Biochem 31:455
Acknowledgements
This research was supported by the International Foundation for Science (IFS), Stockholm, Sweden, and the Organization for the Prohibition of Chemical Weapons, The Hague, Netherlands (OPCW), through grants to the first author. The research capacity building program with Burkina Faso by Swedish Agency for Research Cooperation (SAREC) of the Swedish International Development Cooperation Agency (Sida) has also been instrumental for the team cooperation. We would like to thank Dr Ulrik Ilstedt and the two anonymous reviewers for their valuable comments on the manuscript. We wish to thank Hugues Roméo Bazié for experimental assistance. The Plant, Soil, and Water laboratory of INERA (Ouagadougou) gave assistance in chemical analyses.
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Gnankambary, Z., Bayala, J., Malmer, A. et al. Decomposition and nutrient release from mixed plant litters of contrasting quality in an agroforestry parkland in the south-Sudanese zone of West Africa. Nutr Cycl Agroecosyst 82, 1–13 (2008). https://doi.org/10.1007/s10705-008-9165-3
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DOI: https://doi.org/10.1007/s10705-008-9165-3