Abstract
The aim of this field study was to examine how the development of arbuscular mycorrhizal fungi (AMF) on coal mine spoil banks is affected by the presence of plants with different mycorrhizal status. A 3-year trial was conducted on the freshly created spoil bank Vršany, North-Bohemian coal basin, the Czech Republic. Three plant species – non-mycotrophic annual Atriplex sagittata, highly mycotrophic annual Tripleurospermum inodorum (both dominants of early stages of succession) and facultatively mycotrophic Arrhenatherum elatius (a perennial grass species of the later stage of succession) – were planted on 1 m2 plots over 3 years in different sequences that simulated the progress of succession on spoil banks. The development of AMF populations was monitored by evaluation of mycorrhizal colonization of plant roots and by measurement of the mycorrhizal inoculation potential (MIP) of soil. These two parameters were compared between plots inoculated with the mixture of three AMF isolates – Glomus mosseae BEG95, G. claroideum BEG96 and G. intraradices BEG140 – (“inoculated plots”) and plots exposed only to natural dispersal of AMF propagules (“uninoculated plots”). Highly colonized roots of plants together with a high MIP of soil in uninoculated plots were already found at the end of the first season, indicating rapid natural dispersal of AMF propagules. Root colonization of facultatively mycotrophic and non-mycotrophic plants in later years was affected by the mycorrhizal status of the previous plant species. The MIP of soil continuously increased throughout the experiment; in uninoculated plots, the MIP was temporarily decreased if plant species of higher mycotrophy were replaced by species of lower mycotrophy. The results lead to the conclusion that AMF colonize freshly formed sites very quickly and reproduce or accumulate in the soil, which leads to increasing MIP values. However, this infective potential can be decreased if non-mycotrophic plants predominate on the site.
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Abbreviations
- AMF:
-
arbuscular mycorrhizal fungi
- MIP:
-
mycorrhizal inoculation potential
References
Abbot LK, Robson AD (1981) Infectivity and effectiveness of five endomycorrhizal fungi: competition with indigenous fungi in field soils. Aust J Agric Resour 32:621–630
Allen EB, Allen MF (1980) Natural re-establishment of vesicular–arbuscular mycorrhizae following stripmine reclamation in Wyoming. J Appl Ecol 17:139–147
Allen EB, Allen MF (1984) Competition between plants of different successional stages: mycorrhizae as regulators. Can J Bot 62:2625–2629
Allen EB, Allen MF (1988) Facilitation of succession by the nonmycotrophic colonizer Salsola kali (Chenopodiaceae) on a harsh site: effect of mycorrhizal fungi. Am J Bot 75:257–266
Díaz G, Honrubia M (1995) Effect of native and introduced arbuscular mycorrhizal fungi on growth and nutrient uptake of Lygeum spartum and Anthyllis cytisoides. Biol Plant 37:121–129
Douds DD Jr, Galvez L, Franke-Snyder M, Reider C, Drinkwater LE (1997) Effect of compost addition and crop rotation point upon VAM fungi. Agric Ecosyst Environ 65:257–266
Francis R, Read DJ (1994) The contribution of mycorrhizal fungi to the determination of plant community structure. Plant Soil 159:11–25
Francis R, Read DJ (1995) Mutualism and antagonism in the mycorrhizal symbiosis, with special reference to impacts on plant community structure. Can J Bot 73:S1301–S1309
Giovanetti M, Mosse B (1980) An evaluation of techniques for measuring vesicular–arbuscular mycorrhizal infection in roots. New Phytol 84:489–500
Janos DP (1980) Mycorrhizae influence tropical succession. Biotropica 12:56–64
Johnson NC (1998) Responses of Salsola kali and Panicum virgatum to mycorrhizal fungi, phosphorus and soil organic matter: implications for reclamation. J Appl Ecol 35:86–94
Johnson NC, McGraw AC (1988a) Vesicular–arbuscular mycorrhizae in taconite tailings. I. Incidence and spread of Endogonaceous fungi following reclamation. Agric Ecosyst Environ 21:135–142
Johnson NC, McGraw AC (1988b) Vesicular–arbuscular mycorrhizae in taconite tailings. II. Effects of reclamation practices. Agric Ecosyst Environ 21:143–152
Kabir Z, O’Halloran IP, Hamel C (1997) Overwinter survival of arbuscular mycorrhizal hyphae is favored by attachment to roots but diminished by disturbance. Mycorrhiza 7:197–200
Koske RE, Gemma JN (1989) A modified procedure for staining roots to detect VA mycorrhizas. Mycol Res 92:486–505
Malcová R, Albrechtová J, Vosátka M (2001) The role of the extraradical mycelium network of arbuscular mycorrhizal fungi on the establishment and growth of Calamagrostis epigejos in industrial waste substrates. Appl Soil Ecol 18:129–142
Miller RM, Carnes BA, Moorman TB (1985) Factors influencing survival of vesicular–arbuscular mycorrhiza propagules during topsoil storage. J Appl Ecol 22:259–266
Nagahashi G, Douds DD (2000) Partial separation of root exudates components and their effects upon the growth of germinated spores of AM fungi. Mycol Res 104:1453–1464
Newsham KK, Fitter AH, Watkinson AR (1995) Arbuscular mycorrhiza protect an annual grass from root pathogenic fungi in the field. J Ecol 83:991–1000
Oba H, Tawaraya K, Wagatsuma T (2002) Inhibition of pre-symbiotic hyphal growth of arbuscular mycorrhizal fungus Gigaspora margarita by root exudates of Lupinus ssp. Soil Sci Plant Nutr 48:117–120
Prach K (1987) Succession of vegetation on dumps from strip coal mining. Folia Geobot Phytotax 22:339–354
Püschel D, Rydlová J, Vosátka M (2007a) The development of arbuscular mycorrhiza in two simulated stages of spoil-bank succession. Appl Soil Ecol 35:363–369
Püschel D, Rydlová J, Vosátka M (2007b) Mycorrhiza influences plant community structure in succession on spoil banks. Basic Appl Ecol 8:510–520
Schreiner RP, Koide RT (1993) Mustards, mustard oils and mycorrhizas. New Phytol 123:107–113
Sýkorová Z, Rydlová J, Vosátka M (2003) Establishment of mycorrhizal symbiosis in Gentiana verna. Folia Geobot 38:177–189
van der Heijden MGA (2003) Arbuscular mycorrhizal fungi as a determinant of plant diversity: in search of underlying mechanisms and general principles. In: van der Heijden MGA, Sanders IR (eds) Mycorrhizal ecology. Springer, Berlin, pp 225–242
Vestberg M, Saari K, Kukkonen S, Hurme T (2005) Mycotrophy of crops in rotation and soil amendment with peat influence the abundance and effectiveness of indigenous arbuscular mycorrhizal fungi in field soil. Mycorrhiza 15:447–458
Waaland ME, Allen EB (1987) Relationships between VA mycorrhizal fungi and plant cover following surface mining in Wyoming. J Range Manag 40:271–276
Warner NJ, Allen MF, MacMahon JA (1987) Dispersal agents of vesicular–arbuscular mycorrhizal fungi in a disturbed arid ecosystem. Mycologia 79:721–730
Zak JC, Parkinson D (1983) Effects of surface amendation of two mine spoils in Alberta, Canada, on vesicular–arbuscular mycorrhizal development of slender wheatgrass: a 4-year study. Can J Bot 61:798–803
Acknowledgements
Financial support for this study was provided by the Ministry of Education, Youth and Sports of the Czech Republic (grant no. 1M6798593901) and by the Academy of Sciences of the Czech Republic (grant no. AV0Z60050516).
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Püschel, D., Rydlová, J. & Vosátka, M. Does the sequence of plant dominants affect mycorrhiza development in simulated succession on spoil banks?. Plant Soil 302, 273–282 (2008). https://doi.org/10.1007/s11104-007-9480-5
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DOI: https://doi.org/10.1007/s11104-007-9480-5