Skip Navigation Links.
Collapse <span class="m110 colortj mt20 fontw700">Volume 12 (2024)</span>Volume 12 (2024)
Collapse <span class="m110 colortj mt20 fontw700">Volume 11 (2023)</span>Volume 11 (2023)
Collapse <span class="m110 colortj mt20 fontw700">Volume 10 (2022)</span>Volume 10 (2022)
Collapse <span class="m110 colortj mt20 fontw700">Volume 9 (2021)</span>Volume 9 (2021)
Collapse <span class="m110 colortj mt20 fontw700">Volume 8 (2020)</span>Volume 8 (2020)
Collapse <span class="m110 colortj mt20 fontw700">Volume 7 (2019)</span>Volume 7 (2019)
Collapse <span class="m110 colortj mt20 fontw700">Volume 6 (2018)</span>Volume 6 (2018)
Collapse <span class="m110 colortj mt20 fontw700">Volume 5 (2017)</span>Volume 5 (2017)
Collapse <span class="m110 colortj mt20 fontw700">Volume 4 (2016)</span>Volume 4 (2016)
Collapse <span class="m110 colortj mt20 fontw700">Volume 3 (2015)</span>Volume 3 (2015)
Collapse <span class="m110 colortj mt20 fontw700">Volume 2 (2014)</span>Volume 2 (2014)
Collapse <span class="m110 colortj mt20 fontw700">Volume 1 (2013)</span>Volume 1 (2013)
American Journal of Applied Mathematics and Statistics. 2018, 6(6), 232-238
DOI: 10.12691/AJAMS-6-6-3
Original Research

Selection of Potent Isolates from a Population of Alternaria Alternata, a Leaf Spot Pathogen of Poplar

Kartik Uniyal1, , Girish Chandra2, R.U. Khan3 and Y.P. Singh1

1Forest Pathology Division, Forest Research Institute, Dehra Dun 240 006, India

2Division of Forest Statistics, Indian Council of Forestry Research and Education, Dehra Dun 248 006, India

3Department of Plant Protection, Faculty of Agricultural Sciences, Aligarh Muslim University, Aligarh-202 002, India

Pub. Date: November 09, 2018

Cite this paper

Kartik Uniyal, Girish Chandra, R.U. Khan and Y.P. Singh. Selection of Potent Isolates from a Population of Alternaria Alternata, a Leaf Spot Pathogen of Poplar. American Journal of Applied Mathematics and Statistics. 2018; 6(6):232-238. doi: 10.12691/AJAMS-6-6-3

Abstract

Poplar, an important tree in the agri-silvicultural system, is propagated mainly through cuttings to maintain genetic purity. Monocultures of poplar clones are amenable to many diseases as they have a narrow genetic base. Pathogenic populations have variability in terms of pathogenicity and virulence which are governed by its genetic makeup. Mapping the variability and selection of potential pathogenic isolates for breeding disease resistance remains a challenge. During the survey conducted in poplar nurseries located at different geographical sites, altogether 72 isolates of Alternaria alternata, were collected from four commercial clones of P. deltoides. Three selection methods were attempted to select fifteen potent A. alternata isolates based on growth rate, sporulation and spore size (maximum length and maximum breadth). Initially, Rough Gauging Method which is simply based upon index of sum of the character’s values and Equal Class Interval Method which depends upon the index of class interval scores were applied. To overcome the limitations of the above two methods, Unequal Class Interval Method was proposed based on Coefficient of Variation for each character assessed. The index was constructed using the geometric rather than arithmetic mean as the former normalizes the range, so that, no range dominates the scores assigned to the characters. The proposed method is recommended for the situations when the criterion variable depends upon various growth characters having inherent significant variation among each other.

Keywords

agri-silviculture, class interval, clones, coefficient of variation, geometric mean, order statistic

Copyright

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

References

[1]  Stelzer HE and Goldfarb B 1997. Implementing clonal forestry in south-eastern United States. Canadian Journal of Forestry Research 27: 442-446.
 
[2]  McDonald BA and Linde C 2002. Pathogen population genetics, evolutionary potential, and durable resistance. Annual Review of Phytopathology 40: 349-79.
 
[3]  Tack AJM, Thrall PH, Barrett LG, Burdon JJ and Laine AL 2012. Variation in infectivity and aggressiveness in space and time in wild host–pathogen systems: Causes and consequences. Journal of Evolutionary Biology 25: 1918-36.
 
[4]  Wolfe MS 1985. The current status and prospects of multiline cultivars and variety mixtures for disease resistance. Annual Review of Phytopathology 23: 251-73.
 
[5]  Garrett KA and Mundt CC 1999. Epidemiology in mixed host populations. Phytopathology 89: 984-90.
 
[6]  Mundt CC 2002. Use of multiline cultivars and cultivar mixtures for disease management. Annual Review of Phytopathology 40: 381-410.
 
[7]  Laine AL 2004. Resistance variation within and among host populations in a plant–pathogen metapopulation: Implications for regional pathogen dynamics. Journal of Ecology 92: 990-1000.
 
[8]  Parker IM and Gilbert GS 2004. The evolutionary ecology of novel plant–pathogen interactions. Annual Review of Ecology Evolution and Systematics 35: 675-700.
 
[9]  Friesen TL, Stukenbrock EH, Liu Z, Meinhardt S, Ling H, Faris JD, Rasmussen JB, Solomon PS, McDonald BA and Oliver, RP 2006. Emergence of a new disease as a result of inter-specific virulence gene transfer. Nature Genetics 38: 953-56.
 
[10]  Fisher MC, Henk DA, Briggs CJ, Brownstein JS, Madoff LC, McCraw SL, Gurr SJ 2012. Emerging fungal threats to animal, plant and ecosystem health. Nature 484: 186-94.
 
[11]  Uniyal K 2014. Morphological, physiological and molecular studies on Alternaria leaf spot of poplar. PhD Thesis, Forest Research Institute University, Dehradun, India. 163p.
 
[12]  Sturges H 1926. The choice of a class-interval. Journal of American Statistical Association 21: 65-66.
 
[13]  Dhiman RC and Gandhi JN 2012. Clonal development and diversity in WIMCO’s poplar programme. ENVIS Forestry Bulletin 12 (1) 40-48.
 
[14]  Garrett SD 1956. Biology of root infecting fungi. Cambridge University Press, London. 292p.