Search results

Filters

  • Journals
  • Authors
  • Keywords
  • Date
  • Type

Search results

Number of results: 4
items per page: 25 50 75
Sort by:
Download PDF Download RIS Download Bibtex

Abstract

Salinity is one of the most significant abiotic stress factors influencing crop production, especially in arid and semi-arid regions. Plants’ response to salinity stress depends on the cultivated genotype. A pot experiment was conducted to study the impact of two concentrations of sodium chloride (4 and 6 dS∙m–1) on some physiological and production traits of 58 chickpea genotypes. A genetic variation in the response of the investigated chickpea genotypes for NaCl-induced salinity stress was noted. Studied morphophysiological traits and yield components were affected under salt stress in all genotypes tested. Plant height was observed to have the lowest rate of reduction (32%, 48%) at 4 and 6 dS∙m –1, respectively. Leaf stomatal conductance decreased as salinity increased. Salinity stress conditions affected all studied yield components, but there was a genetic variation in the response of the studied genotypes. Under no stress conditions and compared to the other genotypes, the number of pods was significantly higher in BG362 genotype. The seed number was significantly higher in ILC9076 genotype. The 100 seed weight was significantly higher in the genotype ILC2664. The mean seed yield was significantly higher in ILC9354 and the harvest index was significantly higher in ILC8617. In general, salinity stress caused the reduction of all parameters. We assume that the assessment of tolerance of chickpea ( Cicer arietinum L.) genotypes to salinity stress should be based on a complex of morpho-physiological traits and analysis of yield complement.
Go to article

Authors and Affiliations

Hayat Touchan
1
ORCID: ORCID
Oqba Basal
2
ORCID: ORCID

  1. Aleppo University, Faculty of Agriculture, Department of Field Crops, Aleppo, Syria
  2. University of Debrecen, Faculty of Agricultural and Food Sciences and Environmental Management, Department of Applied Plant Biology, Böszörményi Rd, 138/B, 4032, Debrecen, Hungary
Download PDF Download RIS Download Bibtex

Abstract

Fusarium wilt is one of the most severe diseases of chickpea in the major growing areas of chickpea production in western Iran. To identify Fusarium spp. associated with chickpea plants showing symptoms of yellowing and wilting, 58 chickpea fields were sampled and 106 Fusarium spp. isolates were obtained from six different regions of Kermanshah Province in western Iran during 2018 and 2019 crop seasons. Thirty-six isolates obtained from stem or lower stem tissues were selected for pathogenicity, morphological and molecular identification using polymease chain reaction species-specific primers. Eleven isolates of Fusarium spp. were selected for sequence analyzing the translation elongation factor 1-α (EF-1α), and β-tubulin gene regions. Phylogenetic analysis of concatenated DNA sequences of both gene regions of these isolates plus other taxa revealed that 11 Fusarium spp. isolates were clustered into five distinct groups. Based on the results of morphological and molecular identification five Fusarium species were identified. Pathogenicity tests showed that F. oxysporum f. sp. ciceris and F. redolens isolates had the highest disease incidence on JG–62 and Bivenij cvs. and F. hostae, F. equiseti and F. acuminatum isolates had the lowest disease incidence. No sign of vascular discoloration was observed in longitudinal or transverse sections of chickpea plants affected by F. redolens isolates. Instead, brown to black necrosis was observed on the surface of tap-roots and crowns. No correlation was found between geographical distribution and pathogenicity of isolates. This is the first report of morphological, molecular and pathogenicity characteristics of F. redolens and F. hostae isolated from chickpea stems or lower stems in Iran.
Go to article

Bibliography

polymorphic DNA (RAPD). European Journal of Plant Pathology 107: 237–248. DOI: https://doi.org/10.1023/A:1011294204630
Jendoubi W., Bouhadida M., Boukteb A., Beji M., Kharrat M. 2017. Fusarium wilt affecting chickpea crop. Agriculture 7 (23): 1–16. DOI: https://doi.org/10.3390/agriculture7030023
Leslie J.F., Zeller K.A., Summerell B.A. 2001. Icebergs and species in populations of Fusarium. Physiological and Molecular Plant Pathology 59: 107–117. DOI: 10.1006/pmpp.2001.035
Leslie J.F., Summerell B.A. 2006. The Fusarium laboratory manual. Ames, Iowa: Blackwell Publishing, USA, 388 pp.
Manuchehri A., Mesri A. 1966. Fusarium wilt of chickpea. Iranian Journal of Plant Pathology 3 (3): 1–11.
Mishra P.K., Fox R.T.V., Culham A. 2003. Development of a PCR based assay for rapid and reliable identification of pathogenic Fusaria. FEMS Microbiology Letters 218 (2): 329–332. DOI: https://doi.org/10.1111/j.1574-6968.2003.tb11537.x
Mohammadi H., Banihashemi Z. 2005. Distribution, pathogenicity and survival of Fusarium spp. the causal agents of chickpea wilt and root rot in the Fars province of Iran. Iranian Journal of Plant Pathology 41 (4): 687–708.
Navas-Cortes J.A., Alcala-Jimenez A.R., Hau B., Jimenez- -Diaz R.M. 2000. Influence of inoculum density of race 0 and 5 of Fusarium oxysporum f. sp. ciceris on development of Fusarium wilt in chickpea cultivars. European Journal of Plant Pathology 106: 135–146. DOI: https://doi.org/10.1023/A:1008727815927
Nene Y.L., Haware M.P. 1980. Screening chickpea for resistance to wilt. Plant Disease 64: 379–380.
Nelson P.E., Toussoun T.A., Marasas W.F.O. 1983. Fusarium Species: An Illustrated Manual for Identification. Pennyslvania State University Press, University Park, USA, 193 pp.
Nourollahi K.H., Aliaran A., Younesi H. 2017. Genetic diversity of Fusarium oxysporum f. sp. ciceris isolates causal agent of chickpea wilt in Kermanshah province using microsatellite markers. Novel Genetic 11 (4): 605–615.
O’Donnell K., Cigelnik E. 1997. Two divergent intragenomic rDNA ITS2 types within a monophyletic. Molecular Phylogenetics and Evolution 7 (1): 103–116. DOI: https://doi.org/10.1006/mpev.1996.0376
O’Donnell K., Cigelnik E., Nirenberg H.I. 1998. Molecular systematic and phylogeography of the Gibberella fujikuroi species complex. Mycologia 90 (3): 465–493. DOI: https://doi.org/10.1080/00275514.1998.12026933
Saeedi Sh., Jamali S. 2021. Molecular characterization and distribution of Fusarium isolates from uncultivated soils and chickpea plants in Iran with special reference to Fusarium redolens. Journal of Plant Pathology 103 (4): 167–183. DOI: https://doi.org/10.1007/s42161-020-00698-w
Sharma K.D., Muehlbauer F.J. 2007. Fusarium wilt of chickpea: physiological specialization, genetics of resistance and resistance gene tagging. Euphytica 157 (1–2): 1–14. DOI: https://doi.org/10.1007/s10681-007-9401-y
Shokri J., Javan-Nikkhah M., Rezaei S., Zamanizadeh H.R., Nourollahi Kh. 2020. Molecular identification of the races of Fusarium oxysporum f. sp. ciceris, causal agent of chickpea wilt in western and north western provinces of Iran. Applied Entomology and Phytopathology 88 (1): 11–12. DOI: https://doi.org/10.22092/jaep.2020.126209.1281
Taylor J.W., Jacobson D.J., Kroken S., Kasuga T., Geiser D.M., Hibbett D.S., Fisher M.C. 2001. Phylogenetic species recognition and species concepts in fungi. Fungal Genetics and Biology 31 (1): 21–32. DOI: https://doi.org/10.1006/fgbi.2000.1228
Trapero-Casas A., Jimenez-Diaz R.M. 1985. Fungal wilt and root rot diseases of chickpea in southern Spain. Phytopathology 75 (10): 1146–1151. DOI: https://doi.org/10.1094/ Phyto-75-1146
Wang J., Zheng C. 2012. Characterization of a newly discovered Beauveria bassiana isolate to Franklimiella occidentalis Perganda, a non-native invasive species in China. Microbiology Research 167 (2): 116–120. DOI: https://doi.org/10.1016/j.micres.2011.05.002
Younesi H. 2004. Identification of the physiologic races of Fusarium oxysporum f. sp. ciceris in some west provinces of Iran. In: Proceedings of the 16th Iranian Plant Protection Congress, Tabriz, Iran (in Persian with English summary)
Younesi H., Chehri Kh., Sheikholeslami M., Safaee D., Naseri B. 2019. Effects of sowing date and depth on Fusarium wilt development in chickpea cultivars. Journal of Plant Pathology 102 (2): 343–350. DOI: https//doi/10.1007/s42161-019-00423-2
Zokaee S., Falahati Rastegar M., Jafar Poor B., Bagheri A., Jahanbakhsh Mashhadi V. 2012. Genetic diversity determination of Fusarium oxysporum f. sp. ciceris the causal agent of wilting and chlorosis in chickpea by using RAPD and PCR- -RFLP techniques in Razavi and northern Khorasan provinces. Iranian Journal of Pulses Research 3 (2): 7–16. DOI: https://doi.org/10.22067/ijpr.v1391i2.24531
Go to article

Authors and Affiliations

Hassan Younesi
1
ORCID: ORCID
Mostafa Darvishnia
1
ORCID: ORCID
Eidi Bazgir
1
ORCID: ORCID
Khosrow Chehri
2
ORCID: ORCID

  1. Department of Plant Protection, College of Agriculture and Natural Resources, Lorestan University, Khorramabad, Iran
  2. Department of Biology, Faculty of Sciences, Razi University, Kermanshah, Iran
Download PDF Download RIS Download Bibtex

Abstract

Evaluation of moisture absorption in foodstuffs such as black chickpea is an important stage for skinning and cropping practices. Water uptake process of black chickpea was discussed through normal soaking in four temperature levels of 20, 35, 50 and 65 °C for 18 hours, and then the hydration kinetics was predicted by Peleg’s model and finite difference strategy. Model results showed that with increasing soaking temperature from 20 to 65 °C, Peleg’s rate and Peleg’s capacity constant reduced from 13.368×10-2 to 5.664×10-2 and 9.231×10-3 to 9.138×10-3, respectively. Based on key results, a rise in the medium temperature caused an increase in the diffusion coefficient from 5.24×10-10 m2/s to 4.36×10-9 m2/s, as well. Modelling of moisture absorption of black chickpea was also performed employing finite difference strategy. Comparing the experimental results with those obtained from the analytical solution of the theoretical models revealed a good agreement between predicted and experimental data. Peleg’s model and finite difference technique revealed their predictive function the best at the temperature of 65 °C.

Go to article

Authors and Affiliations

Nesa Dibagar
Stefan Jan Kowalski
Reza Amiri Chayjan
Download PDF Download RIS Download Bibtex

Abstract

In order to evaluate morphological and physiological traits related to drought tolerance and to determine the best criteria for screening and identification of drought-tolerant genotypes, we grew two tolerant genotypes (MCC392, MCC877) and two sensitive genotypes (MCC68, MCC448) of chickpea under drought stress (25% field capacity) and control (100% field capacity) conditions and assessed the effect of drought stress on growth, water relations, photosynthesis, chlorophyll fluorescence and chlorophyll content in the seedling, early flowering and podding stages. Drought stress significantly decreased shoot dry weight, CO2 assimilation rate (A), transpiration rate (E), and Psii photochemical efficiency (Fv/Fm) in all genotypes. In the seedling and podding stages, Psii photochemical efficiency was higher in tolerant genotypes than in sensitive genotypes under drought stress. Water use efficiency (WUE) and CO2 assimilation rate were also higher in tolerant than in sensitive genotypes in all investigated stages under drought stress. Our results indicated that water use efficiency, A and Fv/Fm can be useful markers in studies of tolerance to drought stress and in screening adapted cultivars of chickpea under drought stress.

Go to article

Authors and Affiliations

Raheleh Rahbarian
Ramazanali Khavari-Nejad
Ali Ganjeali
Abdolreza Bagheri
Farzaneh Najafi

This page uses 'cookies'. Learn more