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Non-additive effects of litter mixtures on decomposition of leaf litters in a Mediterranean maquis

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Abstract

Many studies across a range of ecosystems have shown that decomposition in mixed litter is not predictable from single-species results due to synergistic or antagonistic interactions. Some studies also reveal that species composition and relative abundance may be more important than just richness in driving non-additive effects. Most studies on litter decomposition in Mediterranean maquis, an high-diversity shrubby ecosystem, have dealt exclusively with single species. In this study we investigated, at the individual-litter level, as well as at the litter-mixture level, the effect of litter mixing on decomposition of 3-species litter assemblages with different relative abundance of the component litters; we set up two types of litter assemblages that reflected the heterogeneity of bush cover in the inner maquis and at the edge maquis/gaps, as related to the leaf traits, i.e. sclerophylly vs mesophylly. We measured mass loss, decay of lignin, cellulose and ADSS (acid detergent soluble substances) and fungal mycelium ingrowth. The results show that over a 403-day incubation period, the decomposition of individual litters in mixtures deviated from that of monospecific litters and had different directions. In litter mixtures of the sclerophylls Phillyrea angustifolia and Pistacea lentiscus with the mesophyll Cistus, decomposition was lower than expected (antagonistic effect); in the mixtures of litters with similar physical structure (Ph. angustifolia and P. lentiscus with Quercus ilex) decomposition was faster than expected (synergistic effect). When considering the different decomposition phases, both negative and positive effects occurred in Quercus mixtures depending on the phase of decomposition. In both types of 3-species litter assemblages the greatest effect occurred in uneven mixtures rather than in even mixtures. Our results show that species composition drives the direction whilst the decomposability and the relative abundance drive the magnitude of non-additive effects of litter mixing on decomposition.

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References

  • Bardgett RD, Shine A (1999) Linkages between plant litter diversity, soil microbial biomass and ecosystem function in temperate grasslands. Soil Biol Biochem 31:317–321

    Article  CAS  Google Scholar 

  • Berg B, Söderström B (1979) Fungal biomass and nitrogen in decomposing Scots pine needle litter. Soil Biol Biochem 11:339–341

    Article  CAS  Google Scholar 

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

    Book  Google Scholar 

  • Blair JM, Parmelee RW, Beare MH (1990) Decay rates, nitrogen fluxes and decomposer communities in single and mixed-species foliar litter. Ecology 71:1976–1985

    Article  Google Scholar 

  • Bonanomi G, Incerti G, Antignani V, Capodilupo M, Mazzoleni S (2010) Decomposition and nutrient dynamics in mixed litter of Mediterranean species. Plant Soil 331:481–496

    Article  CAS  Google Scholar 

  • Canhoto C, Barlocher F, Graca MAS (2002) The effects of Eucalyptus globulus oils on fungal enzymatic activity. Arch Hydrobiol 154:121–132

    CAS  Google Scholar 

  • Chapman SK, Koch GW (2007) What type of diversity yields synergy during mixed litter decomposition in a natural forest ecosystem? Plant Soil 299:153–162

    Article  CAS  Google Scholar 

  • Chapman SK, Newman GS (2010) Biodiversity at the plant-soil interface: microbial abundance and community structure respond to litter mixing. Oecologia 162:763–769

    Article  PubMed  Google Scholar 

  • Cornelissen JHC, Lavorel S, Garnier E et al (2003) A handbook of protocols for standardised and easy measurements of plant functional traits worldwide. Aust J Bot 51:335–380

    Article  Google Scholar 

  • Cox P, Wilkinson SP, Anderson JM (2001) Effects of fungal inocula on the decomposition of lignin and structural polysaccharides in Pinus sylvestris litter. Biol Fertil Soils 33:246–251

    Article  CAS  Google Scholar 

  • de Graaff MA, Classen AT, Castro HF, Schadt CW (2010) Labile soil carbon inputs mediate the soil microbial community composition and plant residue decomposition rates. New Phytol 188:1055–1064

    Article  PubMed  Google Scholar 

  • De Marco A, Forte A, Gentile AE, Virzo De Santo A (2004) Elemental composition and litter decomposition of Phillyrea angustifolia L. at burned and unburned sites. In: Arianoutsou M, Papanastasis VP (eds) Ecology, Conservation and Management of Mediterranean Climate Ecosystems. Proceedings 10th MEDECOS Conference, Rodi (Grecia), 25 Aprile-1 Maggio 2004. Mill, Rotterdam. ISBN 90 5966 016 1

    Google Scholar 

  • De Marco A, Meola A, Esposito F, Virzo De Santo A (2008) Productivity and modifications of ecosystem processes in gaps of a low Macchia in southern Italy. Web Ecology 8: 55-66

  • FAO (1998) World reference base for soil resources—World Soil Res 84 Rome

  • Fioretto A, Papa S, Fuggi A (2003) Litter-fall and litter decomposition in a low Mediterranean shrubland. Biol Fertil Soils 39:37–44

    Article  CAS  Google Scholar 

  • Fioretto A, Di Nardo C, Papa S, Fuggi A (2005) Lignin and cellulose degradation and nitrogen dynamics during decomposition of three leaf litter species in a Mediterranean ecosystem. Soil Biol Biochem 37:1083–1091

    Article  CAS  Google Scholar 

  • Gallardo A, Merino J (1993) Leaf decomposition in two Mediterranean ecosystems of southwest Spain. Influence of substrate quality. Ecology 74:152–161

    Article  Google Scholar 

  • Gartner TB, Cardon ZG (2004) Decomposition dynamics in mixed-species leaf litter a review. Oikos 104:230–246

    Article  Google Scholar 

  • Gessner MO, Swan CM, Dang CK, McKie BG, Bardgett RD, Wall DH, Hättenschwiler S (2010) Diversity meets decomposition. Trends Ecol Evol 25:372–380

    Article  PubMed  Google Scholar 

  • Harrison AF (1971) The inhibitory effect of oak leaf litter tannins on the growth of fungi, in relation to litter decomposition. Soil Biol Biochem 3:167–172

    Article  CAS  Google Scholar 

  • Hättenschwiler S, Tiunov AV, Scheu S (2005) Biodiversity and litter decomposition in terrestrial ecosystems. Ann Rev Ecol Evol Syst 36:191–218

    Article  Google Scholar 

  • Hector A, Beale AJ, Minns A, Otway SJ, Lawton JH (2000) Consequences of the reduction of plant diversity for litter decomposition: effects through litter quality and microenvironment. Oikos 90:357–371

    Article  Google Scholar 

  • Kazakou E, Violle C, Roumet C, Pintor C, Gimenez O, Garnier E (2009) Litter quality and decomposability of species from a Mediterranean succession depend on leaf traits but not on nitrogen supply. Ann Bot 104:1151–1161

    Article  PubMed  CAS  Google Scholar 

  • Kirk TK, Connors WJ, Zeikus JG (1976) Requirement for a growth substrate during lignin decomposition by two wood-rotting fungi. Appl Environ Microb 32:192–194

    CAS  Google Scholar 

  • Magiatis P, Melliou E, Skaltsounis AL, Chinou IB, Mitaku S (1999) Chemical composition and antimicrobial activity of the essential oils of Pistacia lentiscus var. chia. Planta Med 65:749–752

    Article  PubMed  CAS  Google Scholar 

  • Maisto G, De Marco A, Meola A, Sessa L, Virzo De Santo A (2011) Nutrient dynamics in litter mixtures of four Mediterranean maquis species decomposing in situ. Soil Bio Biochem 43:520–530

    Article  CAS  Google Scholar 

  • McArthur JW, Aho JM, Rader RB et al (1994) Interspecific leaf interactions during decomposition in aquatic and floodplain ecosystems. J N Am Benthol Soc 13:57–67

    Article  Google Scholar 

  • McTiernan KB, Ineson P, Coward PA (1997) Respiration and nutrient release from tree leaf litter mixtures. Oikos 78:527–538

    Article  Google Scholar 

  • Nilsson MC, Gallet C, Wallstedt A (1998) Temporal variability of phenolics and batasin-III in Empetrum hermaphroditum leaves over an eight-year period: interpretation of ecological function. Oikos 81:6–16

    Article  CAS  Google Scholar 

  • Olson FCW (1950) Quantitative estimates of filamenthous algae. Trans Am Microsc Soc 69:272–279

    Article  Google Scholar 

  • Osono T (2007) Ecology of ligninolytic fungi associated with leaf litter decomposition. Ecol Res 22:955–974

    Article  Google Scholar 

  • Rayner ADM, Webber JF (1984) Interspecific mycelial interactions—an overview. In: Jennings DH, Rayner ADM (eds) The ecology and physiology of fungal mycelium. Cambridge University Press, Cambridge, pp 383–417

    Google Scholar 

  • Rotheray TD, Boddy L, Jones TH (2009) Collembola foraging responses to interacting fungi. Ecol Entomol 34:125–132

    Article  Google Scholar 

  • Smith VC, Bradford MA (2003) Do non-additive effects on decomposition in litter-mix experiments result from differences in resource quality between litters? Oikos 102:235–242

    Article  Google Scholar 

  • Söderström BE (1977) Vital staining of fungi in pure cultures and in soil with fluorescein diacetate. Soil Biol Biochem 9:59–63

    Article  Google Scholar 

  • Sundman V, Sivela S (1978) A comment on the membrane filter technique for estimation of length of fungal hyphae in soil. Soil Biol Biochem 10:399–401

    Article  Google Scholar 

  • Swan CM, Gluth MA, Horne CL (2009) Leaf litter species evenness influences non-additive breakdown in a headwater stream. Ecology 90:1650–1658

    Article  PubMed  CAS  Google Scholar 

  • Van Soest PJ, Wine RH (1968) Determination of lignin and cellulose in acid–detergent fibre with permanganate. J Assoc Off Agr Chem 51:780–785

    Google Scholar 

  • Zimmer M (2002) Is decomposition of woodland leaf litter influenced by its species richness? Soil Biol Biochem 34:277–284

    Article  CAS  Google Scholar 

  • Ward SE, Ostle NJ, McNamara NP, Bardgett RD (2010) Litter eveness influences short-term peatland decomposition processes. Oecologia 164:511–520

    Article  PubMed  Google Scholar 

  • 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

    Article  Google Scholar 

Download references

Acknowledgments

We are grateful to the Forest Service of the Castel Volturno Nature Reserve for logistic support and Dr. N. Di Fusco for allowing us to use the field site. We thank Dr. C. Arena for measurement of leaf traits. This study was supported by MIUR - PRIN 2005. Two anonymous reviewers are acknowledged for positive criticism.

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Correspondence to Amalia Virzo De Santo.

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Responsible Editor: Hans Lambers.

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De Marco, A., Meola, A., Maisto, G. et al. Non-additive effects of litter mixtures on decomposition of leaf litters in a Mediterranean maquis. Plant Soil 344, 305–317 (2011). https://doi.org/10.1007/s11104-011-0748-4

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