Ecological importance of soil bacterivores for ecosystem functions

Springer Science and Business Media LLC - Tập 398 - Trang 1-24 - 2015
Jean Trap1, Michael Bonkowski2, Claude Plassard3, Cécile Villenave4, Eric Blanchart1
1Institut de Recherche pour le Développement, UMR Eco & Sols, Montpellier, France
2Department of Terrestrial Ecology, Institut of Zoology, University of Cologne, Köln, Germany
3Institut National de Recherche Agronomique – UMR Eco&Sols, Montpellier, France
4ELISOL Environnement, Congenies, France

Tóm tắt

Bacterivores, mostly represented by protists and nematodes, are a key component of soil biodiversity involved in soil fertility and plant productivity. In the current context of global change and soil biodiversity erosion, it becomes urgent to suitably recognize and quantify their ecological importance in ecosystem functioning. Using meta-analysis tools, we aimed at providing a quantitative synthesis of the ecological importance of soil bacterivores on ecosystem functions. We also intended to produce an overview of the ecological factors that are expected to drive the magnitude of bacterivore effects on ecosystem functions. Bacterivores in soil contributed significantly to numerous key ecosystem functions. We propose a new theoretical framework based on ecological stoichiometry stressing the role of C:N:P ratios in soil, microbial and plant biomass as important parameters driving bacterivore-effects on soil N and P availability for plants, immobilization of N and P in the bacterial biomass, and plant responses in nutrition and growth.

Tài liệu tham khảo

Adl SM, Simpson AGB, Farmer MA, Andersen RA, Anderson OR, Barta JR, Bowser SS, Brugerolle G, Fensome RA, Fredericq S, James TY, Karpov S, Kugrens P, Krug J, Lane CE, Lewis LA, Lodge J, Lynn DH, Mann DG, McCourt RM, Mendoza L, Moestrup Ø, Mozley-Standridge SE, Nerad TA, Shearer CA, Smirnov AV, Spiegel FW, Taylor MFJR (2005) The new higher level classification of eukaryotes with emphasis on the taxonomy of protists. J Eucaryot Microbiol 52:399–451 Adl SM, Simpson AG, Lane CE, Lukeš J, Bass D, Bowser SS, Brown M, Burki F, Dunthorn M, Hampl V, Heiss A, Hoppenrath M, Lara E, leGall L, Lynn DH, McManus H, Mitchell EAD, Mozley-Stanridge SE, Wegener Parfrey L, Pawlowski J, Rueckert S, Shadwick L, Schoch C, Smirnov A, Spiegel FW (2012) The revised classification of eukaryotes. J Eucaryot Microbiol 59:429–514 Ågren GI (2004) The C:N:P stoichiomestry of autotrophs - theory and observations. Ecol Lett 7:185–191 Ågren GI (2008) Stoichiometry and nutrition of plant growth in natural communities. Annu Rev Ecol Syst 39:153–170 Alphei J, Bonkowski M, Scheu S (1996) Protozoa, Nematoda and Lumbricidae in the rhizosphere of Hordelymus europeaus (Poaceae): faunal interactions, response of microorganisms and effects on plant growth. Oecologia 106:111–126 Anderson RV, Coleman DC (1981) Population development and interactions between 2 species of bacteriophagic nematodes. Nematologica 27:6–19 Anderson RV, Elliott ET, McClellan JF, Coleman DC, Cole CV, Hunt HW (1978) Trophic interactions in soils as they affect energy and nutrient dynamics. 3. Biotic interactions of bacteria, amebas, and nematodes. Microb Ecol 4:361–371 Anderson R, Gould W, Woods L, Cambardella C, Ingham R, Coleman D (1983) Organic and inorganic nitrogenous losses by microbivorous nematodes in soil. Oikos 40:75–80 Baath E, Lohm U, Lundgren B, Rosswall T, Soderstrom B, Sohlenius B (1981) Impact of microbial-feeding animals on total soil activity and nitrogen dynamics: a soil microcosm experiment. Oikos 37:257–264 Bardgett RD, Cook R, Yeates GW, Denton CS (1999) The influence of nematodes on below-ground processes in grassland ecosystems. Plant Soil 212:23–33 Barrios E (2007) Soil biota, ecosystem services and land productivity. Ecol Econ 64:269–285 Benizri E, Dedourge O, Dibattista-Leboeuf C, Piutti S, Nguyen C, Guckert A (2002) Effect of maize rhizodeposits on soil microbial community structure. Appl Soil Ecol 21:261–265 Bjornlund L, Rønn R (2008) ‘David and Goliath’ of the soil food web - Flagellates that kill nematodes. Soil Biol Biochem 40:2032–2039 Bjornlund L, Liu MQ, Rønn R, Christensen S, Ekelund F (2012) Nematodes and protozoa affect plants differently, depending on soil nutrient status. Eur J Soil Biol 50:28–31 Blanc C, Sy M, Djigal D, Brauman A, Normand P, Villenave C (2006) Nutrition on bacteria by bacterial-feeding nematodes and consequences on the structure of soil bacterial community. Eur J Soil Biol 42:S70–S78 Bonkowski M (2004) Protozoa and plant growth: the microbial loop in soil revisited. New Phytol 162:617–631 Bonkowski M, Clarholm M (2012) Stimulation of plant growth through interactions of bacteria and protozoa: testing the auxiliary microbial loop hypothesis. Acta Protozool 51:237–247 Bonkowski M, Schaefer M (1997) Interactions between earthworms and soil protozoa: a trophic component in the soil food web. Soil Biol Biochem 29:499–502 Bonkowski M, Griffiths B, Scrimgeour C (2000) Substrate heterogeneity and microfauna in soil organic ‘hotspots’ as determinants of nitrogen capture and growth of ryegrass. Appl Soil 14:37–53 Bonkowski M, Geoghegan IE, Birch ANE, Griffiths BS (2001a) Effects of soil decomposer invertebrates (protozoa and earthworms) on an above-ground phytophagous insect (cereal aphid) mediated through changes in the host plant. Oikos 95:441–450 Bonkowski M, Jentschke G, Scheu S (2001b) Contrasting effects of microbial partners in the rhizosphere: interactions between Norway Spruce seedlings (Picea abies Karst.), mycorrhiza (Paxillus involutus (Batsch) Fr.) and naked amoebae (protozoa). Appl Soil 18:193–204 Bonkowski M, Villenave C, Griffiths B (2009) Rhizosphere fauna: the functional and structural diversity of intimate interactions of soil fauna with plant roots. Plant Soil 321:213–233 Bonkowski M, Koller R, Jousset AJF (2011) How protozoa structure microbial communities in the rhizosphere of plants. J Phycol 47:S7 Borkott H (1989) Elementgehalte (C, N, P, K) wirbelloser Bodentiere. Z Pflanzenernähr Bodenkd 152:77–80 Bossio DA, Girvan MS, Verchot L, Bullimore J, Borelli T, Albrecht A, Scow KM, Ball AS, Pretty JN, Osborn AM (2005) Soil microbial community response to land use change in an agricultural landscape of western Kenya. Microb Ecol 49:50–62 Brown LK, George TS, Barrett GE, Hubbard SF, White PJ (2013) Interactions between root hair length and arbuscular mycorrhizal colonisation in phosphorus deficient barley (Hordeum vulgare). Plant Soil 372:195–205 Brussaard L (1997) Biodiversity and ecosystem functioning in soil. Ambio 26:563–570 Brussaard L, De Ruiter PC, Brown GG (2007) Soil biodiversity for agricultural sustainability. Agr Ecosyst Environ 121:233–244 Cappellazzo G, Lanfranco L, Fitz M, Wipf D, Bonfante P (2008) Characterization of an amino acid permease from the endomycorrhizal fungus Glomus mosseae. Plant Physiol 147:429–437 Chen X, Liu M, Hu F, Mao X, Li H (2007) Contributions of soil micro-fauna (protozoa and nematodes) to rhizosphere ecological functions. Acta Ecol Sin 27:3132–3143 Cheng YH, Jiang Y, Griffiths BS, Li DM, Hu F, Li HX (2011) Stimulatory effects of bacterial-feeding nematodes on plant growth vary with nematode species. Nematology 13:369–372 Clarholm M (1985a) Interactions of bacteria, protozoa and plants leading to mineralization of soil-nitrogen. Soil Biol Biochem 17:181–187 Clarholm M (1985b) Possible roles for roots, bacteria, protozoa, and fungi in supplying nitrogen to plants. In: Fitter AH (ed) Ecological interactions in soil. Blackwell Scient. Publ., pp 355–365 Cleveland CC, Liptzin D (2007) C: N: P stoichiometry in soil: is there a “Redfield ratio” for the microbial biomass? Biogeochemistry 85:235–252 Cole CV, Elliott ET, Hunt HW, Coleman DC (1978) Trophic interactions in soils as they affect energy and nutrient dynamics. Phosphorus transformations. Microb Ecol 4:381–387 Coleman DC, Wall DH (2015) Soil fauna: occurrence, biodiversity, and roles in ecosystem function. In: Paul EA (ed) Soil Microbiology, Ecology and Biochemistry, 4th edn. Academic, Boston, pp 111–149 Coleman DC, Cole CV, Anderson RV, Blaha M, Campion MK, Clarholm M, Elliott ET, Hunt HW, Shaefer B, Sinclair J (1977) An analysis of rhizosphere-saprophage interactions in terrestrial ecosystems. Ecol Bull 25:299–309 Coleman DC, Anderson RV, Cole CV, Elliott ET, Woods L, Campion MK (1978) Trophic interactions in soils as they affect energy and nutrient dynamics. Flows of metabolic and biomass carbon. Microb Ecol 4:373–380 Courty PE, Pouysegur R, Buée M, Garbaye J (2006) Laccase and phosphatase activities of the dominant ectomycorrhizal types in a lowland oak forest. Soil Biol Biochem 38:1219–1222 Couteaux MM, Darbyshire JF (1998) Functional diversity amongst soil protozoa. Appl Soil 10:229–237 Cowling AJ (1994) Protozoa distribution and adaptation. In: Darbyshire JF (ed) Soil protozoa. CAB International, London, pp 5–42 Crotty FV, Adl SM, Blackshaw RP, Murray PJ (2013) Measuring soil protist respiration and ingestion rates using stable isotopes. Soil Biol Biochem 57:919–921 Darbyshire JF (1994) Soil protozoa. CAB International, London Darbyshire JF, Davidson MS, Chapman SJ, Ritchie S (1994) Excretion of nitrogen and phosphorus by the soil Ciliate Colpoda steinii when fed the soil bacterium Arthrobacter sp. Soil Biol Biochem 26:1193–1199 De Ley P (1992) The nematode community of a marginal soil at Camberene, Senegal, with special attention to functional morphology and niche partitioning in the family Cephalobidae. Mededelingen van de Koninklijke. Academie voor Wetenschappen, Letteren en Schone Kunsten van België, Klasse der Wetenschappen 53:109–153 De Telegdy‐Kovats L (1932) The growth and respiration of bacteria in sand cultures in the presence and absence of protozoa. Ann Appl Biol 19:65–86 de Vries FT, Thebault E, Liiri M, Birkhofer K, Tsiafouli MA, Bjornlund L, Bracht Jørgensen H, Vincent Brady M, Christensen S, de Ruiter PC, d’Hertefeldt T, Frouz J, Hedlund K, Hemerik L, Gera Hol WH, Hotes S, Mortimer SR, Setala H, Sgardelis SP, Uteseny K, van der Putten WH, Wolters V, Bardgett RD (2013) Soil food web properties explain ecosystem services across European land use systems. Proc Natl Acad Sci U S A 110:14296–14301 Decaëns T (2010) Macroecological patterns in soil communities. Global Ecol Biogeogr 19:287–302 Djigal D, Brauman A, Diop TA, Chotte JL, Villenave C (2004) Influence of bacterial-feeding nematodes (Cephalobidae) on soil microbial communities during maize growth. Soil Biol Biochem 36:323–331 Djigal D, Baudoin E, Philippot L, Brauman A, Villenave C (2010) Shifts in size, genetic structure and activity of the soil denitrifier community by nematode grazing. Eur J Soil Biol 46:112–118 Drevon J-J, Hartwig UA (1997) Phosphorus deficiency increases the argon-induced decline of nodule nitrogenase activity in soybean and alfalfa. Planta 201:463–469 Dupouey J-L, Dambrine E, Laffite J-D, Moares C (2002) Irreversible impact of past land use on forest soils and biodiversity. Ecology 83:2978–2984 Ekelund F (1996) Growth kinetics of five common heterotrophic soil flagellates. Eur J Soil Biol 32:15–24 Ekelund F, Rønn R (1994) Notes on protozoa in agricultural soil with emphasis on heterotrophic flagellates and naked amebas and their ecology. FEMS Microbiol Rev 15:321–353 Ekelund F, Saj S, Vestergard M, Bertaux J, Mikola J (2009) The “soil microbial loop” is not always needed to explain protozoan stimulation of plants. Soil Biol Biochem 41:2336–2342 Elliott E, Cole C, Coleman D, Anderson R, Hunt H, McClellan J (1979) Amoebal growth in soil microcosms: a model system of C, N, and P. Trophic dynamics. Int J Environ Stud 13:169–174 Elliott ET, Anderson RV, Coleman DC, Cole CV (1980) Habitable pore-space and microbial trophic interactions. Oikos 35:327–335 Elser JJ, Urabe J (1999) The stoichiometry of consumer-driven nutrient recycling: theory, observations, and consequences. Ecology 80:735–751 Elser JJ, Sterner RW, Gorokhova E, Fagan WF, Markow TA, Cotner JB, Harrison JF, Hobbie SE, Odell GM, Weider LW (2000) Biological stoichiometry from genes to ecosystems. Ecol Lett 3:540–550 Elser JJ, Acharya K, Kyle M, Cotner J, Makino W, Markow T, Watts T, Hobbie S, Fagan W, Schade J, Hood J, Sterner RW (2003) Growth rate–stoichiometry couplings in diverse biota. Ecol Lett 6:936–943 Fanin N, Fromin N, Buatois B, Hattenschwiler S (2013) An experimental test of the hypothesis of non-homeostatic consumer stoichiometry in a plant litter-microbe system. Ecol Lett 16:764–772 Fenner M, Lee W (1989) Growth of seedlings of pasture grasses and legumes deprived of single mineral nutrients. J Appl Ecol 26:223–232 Ferris H, Venette RC, Lau SS (1997) Population energetics of bacterial-feeding nematodes: carbon and nitrogen budgets. Soil Biol Biochem 29:1183–1194 Ferris H, Venette RC, van der Meulen HR, Lau SS (1998) Nitrogen mineralization by bacterial-feeding nematodes: verification and measurement. Plant Soil 203:159–171 Finlay RD (2008) Ecological aspects of mycorrhizal symbiosis: with special emphasis on the functional diversity of interactions involving the extraradical mycelium. J Exp Bot 59:1115–1126 Foissner W (1999) Soil protozoa as bioindicators: pros and cons, methods, diversity, representative examples. Agric Ecosyst Environ 74:95–112 Foley JA, DeFries R, Asner GP, Barford C, Bonan G, Carpenter SR, Chapin FS, Coe MT, Daily GC, Gibbs HK, Helkowski JH, Holloway T, Howard EA, Kucharik CJ, Monfreda C, Patz JA, Prentice IC, Ramankutty N, Snyder PK (2005) Global consequences of land use. Science 309:570–574 Fürst von Lieven A (2003) Functional morphology and evolutionary origin of the three-part pharynx in nematodes. Zoology 106:183–201 Gallet-Budynek A, Brzostek E, Rodgers VL, Talbot JM, Hyzy S, Finzi AC (2009) Intact amino acid uptake by northern hardwood and conifer trees. Oecologia 160:129–138 Gardi C, Jeffery S, Saltelli A (2013) An estimate of potential threats levels to soil biodiversity in EU. Glob Change Biol 19:1538–1548 Geisen S, Fiore-Donno AM, Walochnik J, Bonkowski M (2014) Acanthamoeba everywhere: high diversity of Acanthamoeba in soils. Parasitol Res 113:3151–3158 Geisen S, Tveit AT, Clark IM, Richter A, Svenning MM, Bonkowski M, Urich T (2015) Metatranscriptomic census of active protists in soils. ISME J. doi:10.1038/ismej.2015.30 Glücksman E, Bell T, Griffiths RI, Bass D (2010) Closely related protist strains have different grazing impacts on natural bacterial communities. Environ Microbiol 12:3105–3113 Gould WD, Coleman DC, Rubink AJ (1979) Effect of bacteria and amoebae on rhizosphere phosphatase activity. Appl Environ Microb 37:943–946 Griffiths BS (1994) Soil nutrient flow. In: Darbyshire JF (ed) Soil protozoa. CAB International, Oxford, pp 65–92 Griffiths BS, Ritz K (1988) A technique to extract, enumerate and measure protozoa from mineral soils. Soil Biol Biochem 20:163–173 Griffiths BS, Bonkowski M, Dobson G, Caul S (1999) Changes in soil microbial community structure in the presence of microbial-feeding nematodes and protozoa. Pedobiologia 43:297–304 Griffiths BS, Spilles A, Bonkowski M (2012) C: N: P stoichiometry and nutrient limitation of the soil microbial biomass in a grazed grassland site under experimental P limitation or excess. Ecol Process 1:1–11 Gusewell S (2004) N: P ratios in terrestrial plants: variation and functional significance. New Phytol 164:243–266 Hanley M, Fenner M (1997) Seedling growth of four fire‐following Mediterranean plant species deprived of single mineral nutrients. Funct Ecol 11:398–405 Hedges LV, Gurevitch J, Curtis PS (1999) The meta-analysis of response ratios in experimental ecology. Ecology 80:1150–1156 Herdler S, Kreuzer K, Scheu S, Bonkowski M (2008) Interactions between arbuscular mycorrhizal fungi (Glomus intraradices, Glomeromycota) and amoebae (Acanthamoeba castellanii, Protozoa) in the rhizosphere of rice (Oryza sativa). Soil Biol Biochem 40:660–668 Hinsinger P (2001) Bioavailability of soil inorganic P in the rhizosphere as affected by root-induced chemical changes: a review. Plant Soil 237:173–195 Hinsinger P, Brauman A, Devau N, Gerard F, Jourdan C, Laclau JP, Le Cadre E, Jaillard B, Plassard C (2011) Acquisition of phosphorus and other poorly mobile nutrients by roots. Where do plant nutrition models fail? Plant Soil 348:29–61 Hodge A, Robinson D, Fitter A (2000) Are microorganisms more effective than plants at competing for nitrogen? Trends Plant Sci 5:304–308 Horiuchi J-i, Prithiviraj B, Bais HP, Kimball BA, Vivanco JM (2005) Soil nematodes mediate positive interactions between legume plants and rhizobium bacteria. Planta 222:848–857 Ingham RE, Trofymow J, Ingham ER, Coleman DC (1985) Interactions of bacteria, fungi, and their nematode grazers: effects on nutrient cycling and plant growth. Ecol Monogr 55:119–140 Irshad U, Villenave C, Brauman A, Plassard C (2011) Grazing by nematodes on rhizosphere bacteria enhances nitrate and phosphorus availability to Pinus pinaster seedlings. Soil Biol Biochem 43:2121–2126 Irshad U, Brauman A, Villenave C, Plassard C (2012) Phosphorus acquisition from phytate depends on efficient bacterial grazing, irrespective of the mycorrhizal status of Pinus pinaster. Plant Soil 358:148–161 Jentschke G, Bonkowski M, Godbold DL, Scheu S (1995) Soil protozoa and forest tree growth - Non-nutritional effects and interaction with mycorrhizae. Biol Fert Soils 20:263–269 Jones DL, Nguyen C, Finlay RD (2009) Carbon flow in the rhizosphere: carbon trading at the soil-root interface. Plant Soil 321:5–33 Jousset A (2011) Ecological and evolutive implications of bacterial defences against predators. Environ Microbiol 14:1830–1843 Jousset A, Lara E, Wall LG, Valverde C (2006) Secondary metabolites help biocontrol strain Pseudomonas fluorescens CHA0 to escape protozoan grazing. Appl Environ Microb 72:7083–7090 Jousset A, Scheu S, Bonkowski M (2008) Secondary metabolite production facilitates establishment of rhizobacteria by reducing both protozoan predation and the competitive effects of indigenous bacteria. Funct Ecol 22:714–719 Jousset A, Rochat L, Péchy-Tarr M, Keel C, Scheu S, Bonkowski M (2009) Predators promote defence of rhizosphere bacterial populations by selective feeding on non-toxic cheaters. ISME J 3:666–674 Jousset A, Rochat L, Scheu S, Bonkowski M, Keel C (2010) Predator–prey chemical warfare determines the expression of biocontrol genes by rhizosphere-associated Pseudomonas fluorescens. Appl Environ Microb 76:5263–5268 Kibblewhite MG (2012) Definition of priority areas for soil protection at a continental scale. Soil Use Manage 28:128–133 Kibblewhite MG, Ritz K, Swift MJ (2008) Soil health in agricultural systems. Philos T Roy Soc B 363:685–701 Koller R, Robin C, Bonkowski M, Ruess L, Scheu S (2013a) Litter quality as driving factor for plant nutrition via grazing of protozoa on soil microorganisms. FEMS Microbiol Ecol 85:241–250 Koller R, Rodriguez A, Robin C, Scheu S, Bonkowski M (2013b) Protozoa enhance foraging efficiency of arbuscular mycorrhizal fungi for mineral nitrogen from organic matter in soil to the benefit of host plants. New Phytol 199:203–211 Koller R, Scheu S, Bonkowski M, Robin C (2013c) Protozoa stimulate N uptake and growth of arbuscular mycorrhizal plants. Soil Biol Biochem 65:204–210 Kreuzer K, Adamczyk J, Iijima M, Wagner M, Scheu S, Bonkowski M (2006) Grazing of a common species of soil protozoa (Acanthamoeba castellanii) affects rhizosphere bacterial community composition and root architecture of rice (Oryza sativa L.). Soil Biol Biochem 38:1665–1672 Krome K, Rosenberg K, Bonkowski M, Scheu S (2009a) Grazing of protozoa on rhizosphere bacteria alters growth and reproduction of Arabidopsis thaliana. Soil Biol Biochem 41:1866–1873 Krome K et al (2009b) Soil bacteria and protozoa affect root branching via effects on the auxin and cytokinin balance in plants. Plant Soil 328:191–201 Kuikman PJ, Van Veen JA (1989) The impact of protozoa on the availability of bacterial nitrogen to plants. Biol Fert Sci 8:13–18 Kuikman PJ, Jansen AG, Van Veen JA, Zehnder AJB (1990) Protozoan predation and the turnover of soil organic-carbon and nitrogen in the presence of plants. Biol Fert Sci 10:22–28 Kuikman PJ, Jansen AG, Van Veen JA (1991) N-15-nitrogen mineralization from bacteria by protozoan grazing at different soil-moisture regimes. Soil Biol Biochem 23:193–200 Kuzyakov Y, Xu X (2013) Competition between roots and microorganisms for nitrogen: mechanisms and ecological relevance. New Phytol 198:656–669 Lambshead P (1993) Recent developments in marine benthic biodiversity research. Oceanis 19:5 Lambshead P, Chen Z, Chen W, Chen S, Dickson S (2004) Marine nematode biodiversity. In: Chen ZX et al. (ed) Nematology: Advances and Perspectives. CAB International, pp 436–467 Lavelle P, Spain AV (2001) Soil Ecology. Kluwer, Dordrecht Leake JR, Johnson D, Donnelly DP, Muckle GE, Boddy L, Read DJ (2004) Networks of power and influence: the role of mycorrhizal mycelium in controlling plant communities and agroecosystem functioning. Can J Bot-Rev Can Bot 82:1016–1045 Lennox LB, Alexander M (1981) Fungicide enhancement of nitrogen fixation and colonization of Phaseolus vulgaris by Rhizobium phaseoli. Appl Environ Microb 41:404–411 Levrat P, Pussard M, Alabouvette C (1992) Enhanced bacterial metabolism of a Pseudomonas strain in response to the addition of culture filtrate of a bacteriophagous amoeba. Eur J Protistol 28:79–84 Louche J, Ali MA, Cloutier-Hurteau B, Sauvage F-X, Quiquampoix H, Plassard C (2010) Efficiency of acid phosphatases secreted from the ectomycorrhizal fungus Hebeloma cylindrosporum to hydrolyse organic phosphorus in podzols. FEMS Microbiol Ecol 73:323–335 Manzoni S, Taylor P, Richter A, Porporato A, Ågren GI (2012) Environmental and stoichiometric controls on microbial carbon‐use efficiency in soils. New Phytol 196:79–91 Marmeisse R, Guidot A, Gay G, Lambilliotte R, Sentenac H, Combier JP, Melayah D, Fraissinet-Tachet L, Debaud JC (2004) Hebeloma cylindrosporum - a model species to study ectomycorrhizal symbiosis from gene to ecosystem. New Phytol 163:481–498 Matz C, Kjelleberg S (2005) Off the hook–how bacteria survive protozoan grazing. Trends Microbiol 13:302–307 Mazzola M, de Bruijn I, Cohen MF, Raaijmakers JM (2009) Protozoan-induced regulation of cyclic lipopeptide biosynthesis is an effective predation defense mechanism for Pseudomonas fluorescens. Appl Environ Microb 75:6804–6811 Meier IC, Avis PG, Phillips RP (2013) Fungal communities influence root exudation rates in pine seedlings. FEMS Microbiol Ecol 83:585–595 Mooshammer M, Wanek W, Hämmerle I, Fuchslueger L, Hofhansl F, Knoltsch A, Schnecker J, Takriti M, Watzka M, Wild B, Keiblinger KM, Zechmeister-Boltenstern S, Richter A (2014a) Adjustment of microbial nitrogen use efficiency to carbon: nitrogen imbalances regulates soil nitrogen cycling. Nat Commun 5:1–7 Mooshammer M, Wanek W, Zechmeister-Boltenstern S, Richter A (2014b) Stoichiometric imbalances between terrestrial decomposer communities and their resources: mechanisms and implications of microbial adaptations to their resources. Front Microbiol 5:1–10 Nasholm T, Kielland K, Ganeteg U (2009) Uptake of organic nitrogen by plants. New Phytol 182:31–48 Neff JC, Chapin FS III, Vitousek PM (2003) Breaks in the cycle: dissolved organic nitrogen in terrestrial ecosystems. Front Ecol Environ 1:205–211 Neidig N, Jousset A, Nunes F, Bonkowski M, Paul RJ, Scheu S (2010) Interference between bacterial feeding nematodes and amoebae relies on innate and inducible mutual toxicity. Funct Ecol 24:1133–1138 Olsson PA, Baath E, Jakobsen I, Söderstrom B (1996) Soil bacteria respond to presence of roots but not to mycelium of arbuscular mycorrhizal fungi. Soil Biol Biochem 28:463–470 Parry JD (2004) Protozoan grazing of freshwater biofilms. Adv Appl Microbiol 54:167–196 Peters JL, Sutton AJ, Jones DR, Abrams KR, Rushton L (2006) Comparison of two methods to detect publication bias in meta-analysis. Jama-J Am Med Assoc 295:676–680 Pimentel D (2006) Soil erosion: a food and environmental threat. Environ Dev Sust 8:119–137 Plassard C, Dell B (2010) Phosphorus nutrition of mycorrhizal trees. Tree Physiol 30:1129–1139 Plassard C, Bonafos B, Touraine B (2000) Differential effects of mineral and organic N sources, and of ectomycorrhizal infection by Hebeloma cylindrosporum, on growth and N utilization in Pinus pinaster. Plant Cell Environ 23:1195–1205 Plassard C, Louche J, Ali MA, Duchemin M, Legname E, Cloutier-Hurteau B (2011) Diversity in phosphorus mobilisation and uptake in ectomycorrhizal fungi. Ann For Sci 68:33–43 Postma-Blaauw M, de Vries FT, De Goede R, Bloem J, Faber J, Brussaard L (2005) Within-trophic group interactions of bacterivorous nematode species and their effects on the bacterial community and nitrogen mineralization. Oecologia 142:428–439 Puglisi E, Pascazio S, Suciu N, Cattani I, Fait G, Spaccini R, Crecchio C, Piccolo A, Trevisan M (2013) Rhizosphere microbial diversity as influenced by humic substance amendments and chemical composition of rhizodeposits. J Geochem Explor 129:82–94 Pussard M, Alabouvette C, Levrat P (1994) Protozoan interactions with the soil microflora and possibilities for biocontrol of plant pathogens. In: Darbyshire JF (ed) Soil Protozoa. CAB International, Oxford, pp 123–146 Ramirez C, Alexander M (1980) Evidence suggesting protozoan predation on Rhizobium associated with germinating seeds and in the rhizosphere of beans (Phaseolus vulgaris L.). Appl Environ Microb 40:492–499 Rønn R, McCaig AE, Griffiths BS, Prosser JI (2002) Impact of protozoan grazing on bacterial community structure in soil microcosms. Appl Environ Microb 68:6094–6105 Rønn R, Vestergard M, Ekelund F (2012) Interactions between bacteria, protozoa and nematodes in soil. Acta Protozool 51:223–235 Rosenberg K, Bertaux J, Krome K, Hartmann A, Scheu S, Bonkowski M (2009) Soil amoebae rapidly change bacterial community composition in the rhizosphere of Arabidopsis thaliana. ISME J 3:675–684 Saleem M, Fetzer I, Dormann CF, Harms H, Chatzinotas A (2012) Predator richness increases the effect of prey diversity on prey yield. Nat Commun 3:1305 Sardans J, Rivas-Ubach A, Penuelas J (2012) The elemental stoichiometry of aquatic and terrestrial ecosystems and its relationships with organismic lifestyle and ecosystem structure and function: a review and perspectives. Biogeochemistry 111:1–39 Schlaghamersky J, Eisenhauer N, Frelichc LE (2014) Earthworm invasion alters enchytraeid community composition and individual biomass in northern hardwood forests of North America. Appl Soil 83:159–169 Sinsabaugh RL, Manzoni S, Moorhead DL, Richter A (2013) Carbon use efficiency of microbial communities: stoichiometry, methodology and modelling. Ecol Lett 16:930–939 Smith SE, Read DJ (2008) Mycorrhizal symbiosis, 3rd edn. Academic, London Somasundaram S, Bonkowski M, Iijima M (2008) Functional role of mucilage-border cells: a complex facilitating protozoan effects on plant growth. Plant Prod Sci 11:344–351 Sundin P, Valeur A, Olsson S, Odham G (1990) Interactions between bacteria-feeding nematodes and bacteria in the rape rhizosphere - Effects on root exudation and distribution of bacteria. FEMS Microbiol Ecol 73:13–22 Tao J, Chen X, Liu M, Hu F, Griffiths B, Li H (2009) Earthworms change the abundance and community structure of nematodes and protozoa in a maize residue amended rice-wheat rotation agro-ecosystem. Soil Biol Biochem 41:898–904 Tibbett M, Sanders FE (2002) Ectomycorrhizal symbiosis can enhance plant nutrition through improved access to discrete organic nutrient patches of high resource quality. Ann Bot-London 89:783–789 Venette RC, Ferris H (1998) Influence of bacterial type and density on population growth of bacterial-feeding nematodes. Soil Biol Biochem 30:949–960 Vitousek PM et al (2002) Towards an ecological understanding of biological nitrogen fixation. Biogeochemistry 57:1–45 Wagg C, Bender SF, Widmer F, van der Heijden MGA (2014) Soil biodiversity and soil community composition determine ecosystem multifunctionality. Proc Natl Acad Sci U S A 111:5266–5270 Wall DH, Bardgett RD, Kelly EF (2010) Biodiversity in the dark. Nat Geosci 3:297–298 Wallenda T, Read DJ (1999) Kinetics of amino acid uptake by ectomycorrhizal roots. Plant Cell Environ 22:179–187 Weekers PH, Bodelier PL, Wijen JP, Vogels GD (1993) Effects of grazing by the free-living soil amoebae Acanthamoeba castellanii, Acanthamoeba polyphaga, and Hartmannella vermiformis on various bacteria. Appl Environ Microb 59:2317–2319 Weisse T (2002) The significance of inter- and intraspecific variation in bacterivorous and herbivorous protists. Anton Leeuw Int J G 81:327–341 Wright DJ (1975) Elimination of nitrogenous compounds by Panagrellus redivivus, Goodey, 1945 (Nematoda: Cephalobidae). Comp Biochem Phys B 52:247–253 Xiao HF, Griffiths B, Chen XY, Liu MQ, Jiao JG, Hu F, Li HX (2010) Influence of bacterial-feeding nematodes on nitrification and the ammonia-oxidizing bacteria (AOB) community composition. Appl Soil 45:131–137 Xu X, Thornton PE, Post WM (2013) A global analysis of soil microbial biomass carbon, nitrogen and phosphorus in terrestrial ecosystems. Global Ecol Biogeogr 22:737–749 Yeates GW (2003) Nematodes as soil indicators: functional and biodiversity aspects. Biol Fert Sci 37:199–210 Yeates G (2007) Abundance, diversity, and resilience of nematode assemblages in forest soils. Can J Forest Res 37:216–225 Zechmeister-Boltenstern S, Keiblinger KM, Mooshammer M, Peñuelas J, Richter A, Sardans J, Wanek W (2015) The application of ecological stoichiometry to plant–microbial–soil organic matter transformations. Ecol Monogr 85:133–155 Zwart KB, Darbyshire JF (1992) Growth and nitrogenous excretion of a common soil flagellate Spumella sp. - a laboratory experiment. J Soil Sci 43:145–157