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Macro- and micronutrient effects on decomposition of leaf litter from two tropical tree species: inferences from a short-term laboratory incubation

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Abstract

While a large number of studies have investigated the effects of macronutrients such as nitrogen (N) or phosphorus (P) on litter decomposition, recent studies suggest that micronutrients including zinc (Zn) may also limit decomposition rates. Our goal was to compare the effects of nutrient addition on decomposition of two leaf litter types from tropical dry forest trees in a short-term laboratory microcosm experiment. Single nutrients (N, P, Zn, potassium, magnesium, and nickel) were applied to leaf litter in solution at low or high concentrations (to mimic in situ availability or to alleviate nutrient limitation, respectively), and decomposition was assessed as final mass remaining and carbon dioxide mineralization. Both mass remaining and CO2 mineralization were affected by nutrient identity and concentration, and these effects varied by species. In general, P and Zn addition increased decomposition, Mg and N inhibited it, and K and Ni had no significant effects. Future studies should consider the interactions between decomposition processes, decomposer communities, and a wider range of macro- and micronutrients.

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References

  • Allison SD, Vitousek PM (2005) Responses of extracellular enzymes to simple and complex nutrient inputs. Soil Biol Biochem 37:937–944

    Article  CAS  Google Scholar 

  • Berg B, McClaugherty C (2008) Plant Litter, Decomposition, Humus Formation, Carbon Sequestration. Springer, Berlin

    Google Scholar 

  • Berg B, Steffen KT, McClaugherty CA (2007) Litter decomposition rate is dependent on litter Mn concentrations. Biogeochemistry 82:29–39

    Article  CAS  Google Scholar 

  • Carreiro MM, Sinsabaugh RL, Repert DA, Parkhurst DF (2000) Microbial enzyme shifts explain litter decay responses to simulated nitrogen deposition. Ecology 81(9):2359–2365

    Article  Google Scholar 

  • Cleveland CC, Reed SC, Townsend AR (2006) Nutrient regulation of organic matter decomposition in a tropical rain forest. Ecology 87:492–503

    Article  PubMed  Google Scholar 

  • Cleveland CC, Townsend AR, Schmidt SK (2002) Phosphorus limitation of microbial processes in moist tropical forests: evidence from short-term laboratory incubations and field studies. Ecosystems 5:680–691

    CAS  Google Scholar 

  • Compton JE, Watrud LS, Porteous LA, DeGrood S (2004) Response of soil microbial biomass and community composition to chronic nitrogen additions at Harvard forest. For Ecol Manage 196:143–158

    Article  Google Scholar 

  • Cornwell WK, Cornelissen JHC, Amatangelo K, Dorrepaa E, Eviner VT, Godoy O, Hobbie SE, Hoorens B, Kurokawa H, Perez-Harguindeguy N, Quested HM, Santiago LS, Wardle DA, Wright IJ, Aerts R, Allison SD, vanBodegom P, Brovkin V, Chatain A, Callaghan TV, Dıaz S, Garnier E, Gurvich DE, Kazakou E, Klein JA, Read J, Reich PB, Soudzilovskaia NA, Vaieretti MV, Westoby M (2008) Plant species traits are the predominant control on litter decomposition rates within biomes worldwide. Ecology Letters 11:1065–1071

    Article  PubMed  Google Scholar 

  • Dail DB, Davidson EA, Chorover J (2001) Rapid abiotic transformation of nitrate in an acid forest soil. Biogeochemistry 54:131–146

    Article  CAS  Google Scholar 

  • Demoling F, Nilsson LO, Baath E (2008) Bacterial and fungal response to nitrogen fertilization in three coniferous forest soils. Soil Biol Biochem 40:370–379

    Article  CAS  Google Scholar 

  • Duarte S, Pascoal C, Alves A, Correia A, Cassio F (2008) Copper and zinc mixtures induce shifts in microbial communities and reduce leaf litter decomposition in streams. Freshwater Biology 53:91–101

    CAS  Google Scholar 

  • Duarte S, Pascoal C, Cassio F (2004) Effects of zinc on leaf decomposition by fungi in streams: studies in microcosms. Microbial Ecology 48:366–374

    Article  PubMed  CAS  Google Scholar 

  • Fog K (1988) The effect of added nitrogen on the rate of decomposition of organic matter. Biological Reviews of the Cambridge Philosophical Society 63:433–462

    Article  Google Scholar 

  • Galicia L, Garcia-Oliva F (2004) The effects of C, N and P additions on soil microbial activity under two remnant tree species in a tropical seasonal pasture. Applied Soil Ecology 26:31–39

    Article  Google Scholar 

  • Gillespie TW, Grijalva A, Farris CN (2000) Diversity, composition, and structure of tropical dry forests in Central America. Plant Ecology 147:37–47

    Article  Google Scholar 

  • Grodziński W, Greszta J, Laskowski R, Maryański M, Rozen A (1990) Effect of the chemical composition of industrial dusts on forest floor organic matter accumulation. Water, Air, and Soil Pollution 53:169–178

    Article  Google Scholar 

  • Groffman PM, Fisk MC, Driscoll CT, Likens GE, Fahey TJ, Eager C, Pardo LH (2006) Calcium additions and microbial nitrogen cycle processes in a northern hardwood forest. Ecosystems 9:1289–1305

    Article  CAS  Google Scholar 

  • Hobbie SE (2005) Contrasting effects of substrate and fertilizer on the early stages of litter decomposition. Ecosystems 8:644–656

    Article  CAS  Google Scholar 

  • Hobbie SE (2008) Nitrogen effects on decomposition: a five-year experiment in eight temperate sites. Ecology 89:2633–2644

    Article  PubMed  Google Scholar 

  • Hobbie SE, Vitousek PM (2000) Nutrient limitation of decomposition in Hawaiian forests. Ecology 81:1867–1877

    Article  Google Scholar 

  • Högberg P, Fan H, Quist M, Binkley D, Tamm CO (2006) Tree growth and soil acidification in response to 30 years of experimental nitrogen loading on boreal forest. Global Change Biology 12:489–499

    Article  Google Scholar 

  • Hughes MN, Poole RK (1989) Metals and Micro-organisms. Chapman and Hall, New York

    Google Scholar 

  • Kaspari M, Garcia MN, Harms KE, Santana M, Wright SJ, Yavitt JB (2008) Multiple nutrients limit litter fall and decomposition in a tropical forest. Ecology Letters 11:35–43

    PubMed  Google Scholar 

  • Kaspari M, Yanoviak SP, Dudley R, Yuan M, Clay NA (2009) Sodium shortage as a constraint on the carbon cycle in an inland tropical rainforest. Proc Nat Acad Sci 106:19405–19409

    Article  PubMed  CAS  Google Scholar 

  • Knorr M, Frey SD, Curtis PS (2005) Nitrogen additions and litter decomposition: a meta-analysis. Ecology 86:3252–3257

    Article  Google Scholar 

  • Lahr J, Kools SAE, vanderHout A, Faber JH (2008) Combined effects of zinc and earthworm density on soil ecosystem functioning. Soil Biol Biochem 40:334–341

    Article  CAS  Google Scholar 

  • Laskowski R, Maryański M, Niklińska M (1994) Effect of heavy metals and mineral nutrients on forest litter respiration rate. Environ Pollution 84:97–102

    Article  CAS  Google Scholar 

  • Lawrence D (2005) Regional-scale variation in litter production and seasonality in tropical dry forests of southern Mexico. Biotropica 37:561–570

    Article  Google Scholar 

  • LeBauer DS, Treseder KK (2008) Nitrogen limitation of net primary productivity in terrestrial ecosystems is globally distributed. Ecology 89:371–379

    Article  PubMed  Google Scholar 

  • Lukumbuzya TK, Fyles JW, Côté B (1994) Effects of base-cation fertilization on litter decomposition in a sugar maple forest in southern Quebec. Can J For Res 24:447–452

    Article  Google Scholar 

  • Manzoni S, Jackson RB, Trofymow JA, Porporato A (2008) The global stoichiometry of litter nitrogen mineralization. Science 321:684–686

    Article  PubMed  CAS  Google Scholar 

  • Marschner H (1995) Mineral nutrition of higher plants, 2nd edn. Academic, San Digeo

    Google Scholar 

  • Martínez-Yrízar A (1995) Biomass distribution and primary productivity of tropical dry forests. In: Bullock SH, Mooney HA, Modesto E (eds) Seasonally dry tropical forests. Cambridge University Press, New York, pp 326–345

    Chapter  Google Scholar 

  • Melillo JM, Aber JD, Muratore JF (1982) Nitrogen and lignin control of hardwood leaf litter decomposition dynamics. Ecology 1982:621–626

    Article  Google Scholar 

  • Muneer M, Oades JM (1989) The role of Ca-organic interactions in soil aggregate stability. I. Laboratory studies with 14 C-glucose, CaCO3 and CaSO4.2H2O. Aust J Soil Res 27:389–399

    Article  CAS  Google Scholar 

  • Pascoal C, Cássio F, Nikolcheva L, Bärlocher F (2010) Realized fungal diversity increases functional stability of leaf litter decomposition under zinc stress. Microb Ecol 59:84–93

    Article  PubMed  CAS  Google Scholar 

  • Powers JS, Becknell JM, Irving J, Perez-Aviles D (2009) Diversity and structure of regenerating tropical dry forests in Costa Rica: geographic patterns and environmental drivers. For Ecol Manage 258:959–970

    Article  Google Scholar 

  • Promputtha I, Lumyong S, Dhanasekaran V, McKenzie EHC, Hyde KD, Jeewon R (2007) A phylogenetic evaluation of whether endophytes become saprotrophs at host senescence. Microb Ecol 53:579–590

    Article  PubMed  Google Scholar 

  • Reich PB, Oleksyn J (2004) Global patterns of plant leaf N and P in relation to temperature and latitude. Proc Nat Acad Sci 101:11001–11006

    Article  PubMed  CAS  Google Scholar 

  • Ruhling A, Tyler G (1973) Heavy metal pollution and decomposition of spruce needle litter. Oikos 24:402–416

    Article  Google Scholar 

  • Sinsabaugh RL (1994) Enzymic analysis of microbial pattern and process. Biol Fert Soils 17:69–74

    Article  CAS  Google Scholar 

  • Sinsabaugh RL, Moorhead DL (1994) Resource allocation to extracellular enzyme production: a model for nitrogen and phosphorus control of litter decomposition. Soil Biol Biochem 26:1305–1311

    Article  Google Scholar 

  • Sinsabaugh RL, Gallo ME, Lauber C, Waldrop MP, Zak DR (2005) Extracellular enzyme activities and soil organic matter dynamics for northern hardwood forests receiving simulated nitrogen deposition. Biogeochemistry 75:201–215

    Article  CAS  Google Scholar 

  • Strickland MS, Lauber C, Fierer N, Bradford MA (2009) Testing the functional significance of microbial community composition. Ecology 90:441–451

    Article  PubMed  Google Scholar 

  • Strojan CL (1978) Forest leaf litter decomposition in the vicinity of a zinc smelter. Oecologia 32:203–212

    Article  Google Scholar 

  • Swift MJ, Heal OW, Anderson JM (1979) Decomposition in terrestrial ecosystems. Studies in Ecology, vol 5. University of California Press, Berkeley

    Google Scholar 

  • Townsend AR, Cleveland CC, Houlton BZ, Alden CB, White JWC (2011) Multi-element regulation of the tropical forest carbon cycle. Front Ecol Environ 9:9–17

    Article  Google Scholar 

  • Treseder KK (2008) Nitrogen additions and microbial biomass: a meta-analysis of ecosystem studies. Ecol Lett 11:1111–1120

    Article  PubMed  Google Scholar 

  • Tyler G (1974) Heavy metal pollution and soil enzymatic activity. Plant Soil 41:303–311

    Article  CAS  Google Scholar 

  • Tyler G (2005) Changes in the concentrations of major, minor and rare-earth elements during leaf senescence and decomposition in a Fagus sylvatica forest. For Ecol Manage 206:167–177

    Article  Google Scholar 

  • Vadeboncoeur MA (2010) Meta-analysis of fertilization experiments indicates multiple limiting nutrients in northeastern deciduous forests. Can J For Res 40:1766–1780

    Article  CAS  Google Scholar 

  • VanSoest PJ (1967) Development of a comprehensive system of feed analysis and its application to forages. J Animal Sci 26:119–128

    Google Scholar 

  • VirzoDeSanto A, DeMarco A, Fierro A, Berg B, Rutigliano FA (2009) Factors regulating litter mass loss and lignin degradation in late decomposition stages. Plant Soil 318:217–228

    Article  CAS  Google Scholar 

  • Vitousek PM (1984) Litter fall, nutrient cycling, and nutrient limitation in tropical forests. Ecology 65:285–298

    Article  CAS  Google Scholar 

  • Vitousek PM (1998) Foliar and litter nutrients, nutrient resorption, and decomposition in Hawaiian Metrosideros polymorpha. Ecosystems 1:401–407

    Article  CAS  Google Scholar 

  • Vitousek PM, Farrington H (1997) Nutrient limitation and soil development: experimental test of a biogeochemical theory. Biogeochemistry 37:63–75

    Article  CAS  Google Scholar 

  • Wackett LP, Dodge AG, Ellis LBM (2004) Microbial genetics and the periodic table. Appl Environ Microbiol 70:647–655

    Article  PubMed  CAS  Google Scholar 

  • Wackett LP, Orme-Johonson WH, Walsh CT (1989) Transition metal enzymes in bacterial metabolism. In: Beveridge TJ, Doyle RJ (eds) Metal Ions and Bacteria. Wiley, New York, pp 165–206

    Google Scholar 

  • Wallenstein MD, McNulty S, Fernandez IJ, Boggs J, Schlesinger WH (2006) Nitrogen fertilization decreases forest soil fungal and bacterial biomass in three long-term experiments. For Ecol Manage 222:459–468

    Article  Google Scholar 

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Acknowledgements

Funding for this study was provided through a NASA New Investigator Award (NS000107) to J. Powers. We thank Peter Tiffin, Carol Adair, David Manning, and two anonymous reviewers for reviews of previous drafts of this manuscript and Jennifer King for allowing us to use her GC.

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Correspondence to Jennifer S. Powers.

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Responsible Editor: Tim Moore.

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Powers, J.S., Salute, S. Macro- and micronutrient effects on decomposition of leaf litter from two tropical tree species: inferences from a short-term laboratory incubation. Plant Soil 346, 245–257 (2011). https://doi.org/10.1007/s11104-011-0815-x

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