Assessment of environmental variables conducive for epidemiology of rice-blast pathosystem

Paper Details

Research Paper 01/08/2015
Views (1072)
current_issue_feature_image
publication_file

Assessment of environmental variables conducive for epidemiology of rice-blast pathosystem

Syed Atif Hasan Naqvi, Rashida Perveen
Int. J. Biosci. 7(2), 199-206, August 2015.
Copyright Statement: Copyright 2015; The Author(s).
License: CC BY-NC 4.0

Abstract

Rice blast-pathosystem is one of most serious disease of rice caused by Pyricularia oryzae. Environmental factors play an important role in sudden outbreaks of rice blast in all rice growing regions of the world. In the current study different environmental factors were explored by correlation and regression analysis to find out their contribution to facilitate the rice blast disease. Maximum disease severity 62.32% and AUDPC (635.35) was calculated on Basmati-2000 while minimum (432.85) was recorded on Basmati-Pak. Environemntal factors viz., Rainfall and relative humidity showed a positive correlation whereas temperature maximum depicted a negative correlation and remained irresponsive in disease development. All of the regression model parameters were significant at P ≤ 0.05 and Rain fall, relative humidity of morning and evening and wind speed significantly contributed to the development of rice blasting pathosystem except sun shine hours and temperature factor. The coefficient of determination (r2) of 0.93 proved the significance of overall regression model accuracy. The model developed as full showed 96% variability towards the advancement of the disease.

Anonymous. 2010a. Pakistan statistical year book. Federal Bureau of Statistics, Statistical division, Karachi, Pakistan.

Anonymous. 2010b. World Rice Production published in The Rice trade august 3rd, 2010.

Food and Agriculure Organization (FAO). (2012). Food and Agricultural organization of United Nations. [8th May 2014] Website: http://FAOSTAT.fao.org

Arshad HM, Khan IJA, Jamil FF. 2008. Screening of rice germplasm against blast and brown spot disease. Pakistan Journal of Phytopatholgy 20, 52-57.

Sesma A, Osbourn AE. 2004. The rice leaf blast pathogen undergoes developmental processes typical of root-infecting fungi. Nature 431(7008), 582-586. PMID:15457264 http://dx.doi.org/10.1038/nature02880

Zeigler RS, Leong SA, Teng P. 1994. Rice blast disease: International Rice Research Institute, Manila, Philippines.

Khan SMN, Javed SMK, Gill MA. 2002. Screening of rice germplasm against blast disease caused by Pyricularia oryzae cav. In: National Conference of Plant Pathology, NARC, and Islamabad. 86-89.

Padmanabhan SY. 1965. Estimating losses from rice blast in India. Pages 203-221 in the rice blast disease. Proceeding of of symposium at IRRI July 1963. The Johns Hopkin Press Baltimore, Maryland.

Teng PS. 1986. Crop losses appraisal in the tropics. Journal of Plant Protection 3, 39-50.

Nuque FL, Bandong JM, Estrada BA, Lapis DB, Torres CQ. 1983. Common diseases of rice. 276-277 p. In: Rice production manual Philippines. University of Philippines, college Laguna, Philippines.

Arshad HM, Khan IJA, Jamil FF. 2008. Screening of rice germplasm against blast and brown spot diseases. Pakistan Journal of Phytopathology 20, 52-57.

Khan SMN, Javed SMK, Gill MA. 2002. Screening of rice germplasm against blast disease caused by Pyricularia oryzae cav. In: National Conference of Plant Pathology, NARC, and Islamabad 86-89.

Nelson PE, Tousson TA, Marasas I. 1983. Fusarium species. An illustrated manual for identification. Penn. State University Press. 193 P.

IRRI 1996. Standard evaluation system for rice. 4th ed. IRRI, Manila, Phillipine.

Anonymous 1996. Standard evaluation system for Rice. International Rice Testing Progress. International Rice Research Institute Report. Philippines.

Shaner G, Finney R. 1977. The effect of nitrogen fertilization on the expression of slow-mildewing in knox wheat. Phytopathology, 67, 1051–1056.

SAS. 2002. Version 8.00 SAS Institute Inc; Cary, North Carolina, USA.

Jeger MJ, Viljanen-Rollinson SLH. 2001. The use of the area under disease progress curve (AUDPC) to assess quantitative disease resistance in crop cultivars. Theoretical and Applied Genetics 102, 32–40. http://dx.doi.org/10.1007/s001220051615.

Greer CA, Webster RK. 2001. Occurrence, Distribution, Epidemiology, Cultivar Reaction, and Management of Rice Blast Disease in California. Plant Pathology 85, 1096-1102.

EI-Refaei MI. 1977. Epidemiology of rice blast disease in the tropics with special reference to the leaf wetness in relation to disease development. Ph.D. thesis, Indian Agricultural research Institute, New Delhi, (India).

Dean RA. 1997. Signal pathways and appressorium morphogenesis. Annual review of phytopathology 35, 211-234. PMid:15012522 http://dx.doi.org/10.1146/annurev.phyto.35.1.211

Hamer JE, Howard RJ, Chumley FG, Valent B. 1988. A mechanism for surface attachment in spores of a plant pathogenic fungus. Science 239, 288-290. PMid: 17769992 http://dx.doi.org/10.1126/science.239.4837.288.

Talbot NJ. 2003.  On  the trail  of  a  cereal  killer: exploring the biology of Magnaporthe grisea. Annual Reviews in Microbiology 57, 177-202. PMid:14527276 http://dx.doi.org/10.1146/annurev.micro.57.030502.090957.

Related Articles

Intra-population genetic diversity modeling of date palm (Phoenix dactylifera L.) population in Niger

Adamou Ibrahim Maman Laouali*, Zango Oumarou, Alio Moussa Abdourazak, Rafiou Abdoulaye, Idi Saidou Sani, Idi Garba Nana Mariama, Bakasso Yacoubou, Int. J. Biosci. 29(3), 62-70, September 2026.

Biocontrol potential of indigenous Trichoderma isolates against Fusarium wilt of cotton in Tanzania: In vitro screening and screen-house validation

Fauzia Khalid Mpiganzila*, Alfonce Leonard, Lidia Munuo, Ernest Mbega, Agatha Aloyce, Int. J. Biosci. 29(3), 44-61, September 2026.

In vitro study of antioxidant, anti-inflammatory and antihyperglycemic activity of medicinal plants

T. K. Nishath*, P. Mathavi, V. Ambikapathy, P. Prakash, A. Panneerselvam, Int. J. Biosci. 29(3), 32-43, September 2026.

Association between the IL13 rs1800925 (-1112C/T) polymorphism and Schistosoma mansoni infection intensity in a population from western Côte d’Ivoire

Bernardin Ahouty Ahouty*, Abla Edwige Sokouri, Georges Bohoussou Kassi, Innocent Allépo Abé, Martial Kassi N’djetchi, Yaya Ouangbo Ouattara, Ornella Karmelle Lydia Dago, Mathurin Yao Koffi, Thomas Konan Konan, Mathurin N’Goran Koffi, Int. J. Biosci. 29(3), 20-31, September 2026.

Abattoir-based surveillance reveals geographic clustering and risk factors for bovine tuberculosis in Tanzania

Yohana Siyajali Anatory*, Beatus Lyimo, Blandina T. Mmbaga, Joram Buza, Int. J. Biosci. 29(3), 11-19, September 2026.

In vitro assessment of the anticancer activity of quinaldic acid against human breast cancer cells (MCF-7)

N. Medhavi, S. M. Sivasankaran, K. Selvakumar, K. Harish, S. Manoharan*, Int. J. Biosci. 29(3), 1-10, September 2026.

In silico molecular docking analysis of quinaldic acid against cancer related targets

N. Medhavi, K. Harish, S. M. Sivasankaran, K. Selvakumar, B. Vidhyambigai, S. Manoharan*, Int. J. Biosci. 29(2), 129-139, August 2026.

First records of Macrogyrodactylus clarii and six species of Quadriacanthus (Monogenea) infecting Clarias gariepinus (Burchell, 1822) across four localities in Senegal

Arfang Diamanka*, Abdou Toure, Sikhou Drame, Cheikh Diop, Ngor Faye, Int. J. Biosci. 29(2), 118-128, August 2026.