Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-25T07:45:05.307Z Has data issue: false hasContentIssue false

Effects of straw incorporation on Rhizoctonia solani inoculum in paddy soil and rice sheath blight severity

Published online by Cambridge University Press:  05 July 2013

H. ZHU
Affiliation:
Key Laboratory of Microbial Control, Anhui Agricultural University, Hefei 230036, People's Republic of China
Z. X. WANG
Affiliation:
Key Laboratory of Microbial Control, Anhui Agricultural University, Hefei 230036, People's Republic of China
X. M. LUO
Affiliation:
Anhui Academy of Forestry, Hefei 230031, People's Republic of China
J. X. SONG
Affiliation:
Key Laboratory of Microbial Control, Anhui Agricultural University, Hefei 230036, People's Republic of China
B. HUANG*
Affiliation:
Key Laboratory of Microbial Control, Anhui Agricultural University, Hefei 230036, People's Republic of China
*
*To whom all correspondence should be addressed. Email: [email protected]

Summary

Incorporation of rice straw into soil has traditionally been an important method of recycling nutrients and improving soil productivity. Currently, although the effects of straw incorporation on disease severity have been documented, the dynamics of the pathogen in soil after straw incorporation are poorly understood. In the present study, rice straw with various proportions of diseased straw was incorporated at three separate locations (SuPu town, SuSong County and FengYang County) in Anhui province, China. The pathogen dynamics in paddy soil and disease severity of sheath blight during two continuous years from April 2010 to April 2012 were investigated. For all three locations, the amount of pathogen inoculum that persisted in the soil increased with increases in the proportion of diseased straw incorporated. Incorporation of 0·3 and 0·5 diseased straw into soil increased the amount of pathogen inoculum in the soil significantly, whereas incorporation of 0·1 diseased straw into soil had no significant effect on the pathogen inoculum compared with the control (no straw incorporated) or disease severity. Incorporation of healthy rice straw (no disease) resulted in a significant decrease in disease severity, whereas proportions of 0·3 and 0·5 diseased straw resulted in a significant increase of disease severity compared with the control. These results suggested that incorporation of diseased straw enhanced pathogen numbers in soil during the whole decomposition period and increased disease severity. To avoid soil-borne disease accumulation, severely diseased straw should be removed from the field or pre-treated before incorporation.

Type
Crops and Soils Research Papers
Copyright
Copyright © Cambridge University Press 2013 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Abdulla, H. M. (2007). Enhancement of rice straw composting by lignocellulolytic Actinomycete strains. International Journal of Agriculture and Biology 9, 106109.Google Scholar
Anderson, A. L. & Huber, D. M. (1965). The plate-profile technique for isolating soil fungi and studying their activity in the vicinity of roots. Phytopathology 55, 592594.Google Scholar
Blank, S. C., Jetter, K., Wick, C. M. & Williams, J. F. (1993). With a ban on burning, incorporating rice straw into soil may become disposal option for growers. California Agriculture 47, 812.Google Scholar
Boosalis, M. G. & Scharen, A. L. (1959). Methods for microscopic detection of Aphanomyces eutiches and Rhizoctonia solani and for isolation of Rhizoctonia solani associated with plant debris. Phytopathology 49, 192198.Google Scholar
Budge, G. E., Shaw, M. W., Colyer, A., Pietravalle, S. & Boonham, N. (2009). Molecular tools to investigate Rhizoctonia solani distribution in soil. Plant Pathology 58, 10711080.Google Scholar
Chidthaisong, A. & Watanabe, I. (1997). Methane formation and emission from flooded rice soil incorporated with 13C-labeled rice straw. Soil Biology and Biochemistry 29, 11731181.Google Scholar
Cintas, N. A. & Webster, R. K. (2001). Effects of rice straw management on Sclerotium oryzae inoculum, stem rot severity, and yield of rice in California. Plant Disease 85, 11401144.Google Scholar
Coventry, E., Noble, R., Mead, A. & Whipps, J. M. (2005). Suppression of Allium white rot (Sclerotium cepivorum) in different soils using vegetable wastes. European Journal of Plant Pathology 111, 101112.Google Scholar
Diab, H. G., Hu, S. & Benson, D. M. (2003). Suppression of Rhizoctonia solani on impatiens by enhanced microbial activity in composted swine waste amended potting mixes. Phytopathology 93, 11151123.Google Scholar
Hoitink, H. A. J. & Boehm, M. J. (1999). Biocontrol within the context of soil microbial communities: a substrate-dependent phenomenon. Annual Review of Phytopathology 37, 427446.CrossRefGoogle ScholarPubMed
Krause, R. A. & Webster, R. K. (1973). Stem rot of rice in California. Phytopathology 63, 518523.Google Scholar
Leigh, M. B., Prouzová, P., Macková, M., Macek, T., Nagle, D. P. & Fletcher, J. S. (2006). Polychlorinated biphenyl (PCB)-degrading bacteria associated with trees in a PCB-contaminated site. Applied and Environmental Microbiology 72, 23312342.Google Scholar
Lewis, J. A. & Papavizas, G. C. (1977). Effect of plant residues on chlamydospore germination of Fusarium solani f. sp. phaseoli and on Fusarium root rot of beans. Phytopathology 67, 925929.Google Scholar
Li, W., Li, D., Twieg, E., Hartung, J. S. & Levy, L. (2008). Optimized quantification of unculturable Candidatus liberibacter spp. in host plants using real-time PCR. Plant Disease 92, 854861.Google Scholar
Lievens, B., Brouwer, M., Vanachter, A. C. R. C., Cammue, B. P. A. & Thomma, B. P. H. J. (2006). Real-time PCR for detection and quantification of fungal and oomycete tomato pathogens in plant and soil samples. Plant Science 171, 155165.Google Scholar
Mandal, K. G., Misra, A. K., Hati, K. M., Bandyopadhyay, K. K., Ghosh, P. K. & Mohanty, M. (2004). Rice residue management options and effects on soil properties and crop. Food, Agriculture and Environment 2, 224231.Google Scholar
McKellar, M. E. & Nelson, E. B. (2003). Compost-induced suppression of Pythium damping-off is mediated by fatty-acid metabolizing seed-colonizing microbial communities. Applied and Environmental Microbiology 69, 452460.CrossRefGoogle ScholarPubMed
Mithrasena, Y. J. P. K., Adhikari, W. P. & Wickramasinghe, D. L. (1989). Studies on sheath blight of rice in the low country wet zone. Tropical Agriculture 145, 7586.Google Scholar
Papavizas, G. C. & Davey, C. B. (1959). Isolation of Rhizoctonia solani Kühn from naturally infested and artificially inoculated soils. Plant Disease Reporter 43, 404410.Google Scholar
Papavizas, G. C. & Davey, C. B. (1960). Rhizoctonia disease of bean as affected by decomposing green plant materials and associated microfloras. Phytopathology 50, 516522.Google Scholar
Ritchie, F., Bain, R. A. & McQuilken, M. P. (2009). Effects of nutrient status, temperature and pH on mycelial growth, sclerotial production and germination of Rhizoctonia solani from potato. Journal of Plant Pathology 91, 589596.Google Scholar
Silgram, M. & Chambers, B. J. (2002). Effects of long-term straw management and fertilizer nitrogen additions on soil nitrogen supply and crop yields at two sites in eastern England. Journal of Agricultural Science, Cambridge 139, 115127.Google Scholar
Singh, S. K., Shukla, V., Singh, H. & Sinha, A. P. (2004). Current status and impact of sheath blight in rice (Oryza sativa L.) - a review. Agricultural Reviews 25, 289297.Google Scholar
Smolinska, U. (2000). Survival of Sclerotium cepivorum sclerotia and Fusarium oxysporum chlamydospores in soil amended with cruciferous residues. Journal of Phytopathology 148, 343349.Google Scholar
Strange, R. N. & Scott, P. R. (2005). Plant disease: a threat to global food security. Annual Review of Phytopathology 43, 83116.Google Scholar
Sweetingham, M. W. (1991). The effect of inoculum distribution and sowing depth on Pleiochaeta root rot of lupins. Australian Journal of Agricultural Research 42, 121128.Google Scholar
Tenuta, M. & Lazarovits, G. (2002). Ammonia and nitrous acid from nitrogenous amendments kill the microsclerotia of Verticillium dahliae. Phytopathology 92, 255264.Google Scholar