Evaluation and response of selected maize genotypes to Stenocarpella maydis in Maseno farm, Maseno (Kenya)

Paper Details

Research Paper 01/08/2017
Views (883)
current_issue_feature_image
publication_file

Evaluation and response of selected maize genotypes to Stenocarpella maydis in Maseno farm, Maseno (Kenya)

George T. Opande, Mathews Dida, Phillip Onyango, Christine Wesonga
Int. J. Biosci. 11(2), 170-175, August 2017.
Copyright Statement: Copyright 2017; The Author(s).
License: CC BY-NC 4.0

Abstract

Maize ear rot disease is caused by Stenocarpella maydis and other ear rot fungus that work in a complex relationship. The disease lowers the quality of the maize cob and grains. Before this study, there was no documented report on the susceptibility of the 9 selected genotypes namely; EH10, EH14, EH15, P3253, H614D, EH13, H516, H515 and EHI6 to S. maydis, therefore information gained on the response of these genotypes to S. maydis would be helpful not only in determining resistance of the 9 genotypes but also provide useful information in the continuous evaluation of germplasm for ear rot resistance. Investigations were conducted on the genotypes that were planted between September – December 2014 and February – July 2015 in the Maseno University farm and analysis conducted at the botany laboratory located within geographical coordinates; 0 1’0’’ S, 34 36’0’N at an altitude of 1503 meters above sea level. The experimental design was Alpha lattice, replicated thrice with nine hybrids. The mean severity scores level for the 9 hybrids was 1.98. EH10, EH14, EH15, and P3253 hybrids were resistant to S maydis H614D, EH13, H516, H515, EHI6 hybrids susceptible to the S. maydis ear rot fungus. S. maydis was also found to be the main ear rot causing fungus in Maseno University farm constituting (8-9%) while Nigrospora caused highest severity score of 3.

Bansiger M, Vivek BS. 1997. Field book: software for managing a maize breeding programme. CIMMYT Mexico.

Christensen JJ, Wilcoxson RD. 1967 Stalk rot of corn. Monograph of the America. Phytopathological Society 3, 59.

Dhanraj KS. 1966. Dry rot maize caused by Diplodia macrospora-.Indian- Phytopathology 19, 120.

Dorrance AE, Hinkelman KH, Warren HL. 1998 Diallel analysis of Diplodia ear rot resistance in maize. Plant Disease 82, 699-703.

Flett BC, Mclaren NW, Wehner FC. 2001. Incidence of Stenpcarpella maydis ear rot of corn under crop rotation systems. Plant disease 85, 92-4.

Flett BC, Van Rensburg JB. 1992. Effect of Busseola fusca on the incidence of maize ear rot caused by Fusarium moniliform and Stenocarpella maydis. In South Africa journal of plant soil 9, 177-179.

Mac Donald MV, Chapman R. 1997.The incidence of Fusarium moniliforme on maize from Central America, Africa and Asia during 1992-1995.

Olantinwo RK, Cardwell A, Menkir M, Julian A. 2004. Inheritance of Resistance  to Stenocarepalla (Earl) Ear Rot of Maize in the Mid-Altitude Zone of Nigeria European Journal of Plant Pathology 105, 535-43.

Patterson HD, Williams ER. 1976. A new class. of resolvable block designs in biometrika 63, 83-92.

Sutton BC, Waterston JM. 1966. Diplopodia maydis. CMI Descriptions of Pathogenic Fungi and Bacteria No.84 CAB International, Wallingford UK.

Vincelli P. 2003. Ear Rot of Corn Caused by Stenocarpella maydis (=Diplodiamaydis) University of Kentucky Cooperative Extension Service. Datasheet PPA- 43 www.ca.uky. edu/agc/pubs/ppa/ ppa43.pdf

Walker JC. 1969. Plant pathology (3rd edition), Pp335,341. Mc Graw-Hill, New York, USA. Zad, J.; Ale Agha, N. (1985) A note on the mycoflora of maize in Iran.

Related Articles

The role of aberrant glycosylation in autoimmune disease development and progression

Md. Nafis Fuad Prottoy, Sayad Md. Didarul Alam*, Int. J. Biosci. 28(6), 1-12, June 2026.

Seasonal variations in bed bug (Cimex spp.) populations in several public places in Korhogo (Ivory Coast): Ecological approaches and epidemiological perspectives

Toure Donatie Serge*, Traore Issouf, Traore Mamadou, Ouattara Manzara, Ouattara Foungoye Allassane, Kone Mouhamadou, Doumbia Mamadou, Int. J. Biosci. 28(5), 76-83, May 2026.

Molecular surveillance of African swine fever virus in raw pork and blood samples from wet markets and abattoirs in Tuguegarao City, Cagayan

Hannah Lee R. Guirren*, Benjamin Abella, Aira D. Cuarteros, Int. J. Biosci. 28(5), 66-75, May 2026.

Limonene-enhanced botanical fungicides: A sustainable component of integrated tomato powdery mildew management in the tropical region

Edmund F. Luena*, Angela G. Mkindi, Akida I. Meya, Nelson S. Mpumi, Steven R. Belmain, Int. J. Biosci. 28(5), 52-65, May 2026.

Kapwa (Shared identity): The case of being community health workers (CHWs) in Cagayan Province, Philippines

Jay Emmanuel L. Asuncion, Julius T. Capili, Jinky Marie T. Chua*, Pauline Grace P. Casil-Batang, Lara Melissa G. Luis, Dorina D. Sabatin, Krisha Anne A. Hipolito, Ethel Marie M. Mangada, Int. J. Biosci. 28(5), 43-51, May 2026.

Effects of corn silage-based diets on carcass and meat characteristics of Philippine native swamp buffalo (Bubalus bubalis carabanensis)

Vince Randolf R. Sumajit*, Phoebe Lyndia T. Llantada, Ann-Sherly R. Dugyon, Int. J. Biosci. 28(5), 36-42, May 2026.

Assessment of the knowledge, attitude, and practices of frontliners toward community-acquired pneumonia in the Cagayan, Philippines

Jinky Marie T. Chua*, Nikko Alexander S. Pacquing, Ann P. Chua, Ethel Marie M. Mangada, Int. J. Biosci. 28(5), 26-35, May 2026.