F. Noor
Department of Botany, Jahangirnagar University, Savar, Dhaka-1342, Bangladesh
F. Hossain
Department of Botany, Jahangirnagar University, Savar, Dhaka-1342, Bangladesh
U. Ara
Institute of Food Science & Technology, Bangladesh Council of Scientific and Industrial Research (BCSIR), Dhaka
Screening; French bean; Genotypes; Yield; Seed proximate
Research field of Bangladesh Council of Scientific and Industrial Research (BCSIR), Dhaka,
Variety and Species
Nine french bean genotypes with the accession numbers, BB-3, BB-5, BB-6, BB-9, BB-10, BB-11, BB-14, BB-15 and BB-20 were collected from Agronomy Division, Bangabandhu Sheikh Mujibur Rahman Agricultural University, Gazipur. Two varieties namely BARI bush bean -1 and BARI bush bean -2 also was collected from Bangladesh Agricultural Research Institute (BARI), Gazipur. The soil samples were analyzed at the Soil Research and Development Institute (SRDI), Farmgate, Dhaka according the Fertilizer Recommendation Guide (Anomymous, 2005). Field experiment was carried out at the research field of Bangladesh Council of Scientific and Industrial Research (BCSIR), Dhaka, in the Rabi season during November 2007 to March 2008 in a randomized complete block design (RCBD) with three replications. The unit plot size was 2.0 m x 1.5 m. Cow dung was applied 6.67 t/ha and Nitrogen, phosphorous, potassium, boron and sulphur were applied as per the recommendation of Fertilizer Recommendation Guide (2005). The seeds were sown with the spacing 30 cm x15 cm in line and about 3.0 cm in depth and covered with pulverized soil and pressed gently by hand (Mozumder 2002). The sowing was done on 20 November, 2007 and then the plots were watered slightly in the line to supply sufficient moisture for quick germination. Weeding was done at 15 days interval. The crop was protected by spraying Malathion 57 EC @ 2 ml/L as per recommendation of BARI (Anomymous, 1995). Furrow irrigation was given at an interval of 7 to 10 days depending on soil moisture content. Plant height, number of leaves, leaf area (Gardner et al.1988), leaf area index (Radford, 1967 and Watson, 1952), disease incidence (Khandaker et al. 2011), pod length, number of pods/plant, number of seeds/pod, 1000 seed weight, fresh pod yield g/plant, seed yield g/plant were measured from ten randomly selected plants for each genotype at the harvest. Data on fresh pod yield t/ha, seed yield (t/ha) and harvest index were taken from the samples of the pre-demarcated area of each plot according to Ullah (Ullah 2006). Days to 4 leaves stage, 90% flowering, pod setting and maturity of pods were counted when each physiological character was appeared in a genotype. Quantitative determination of moisture, crude protein, crude fiber, crude fat, ash and carbohydrate of dry seeds were done according to Association of Official Analytical Chemist (AOAC) (Anomymous, 2005). Statistical analysis All the data collected on various parameters were statistically analyzed by SPSS (version 13) and MS Excel programme. Analysis of variance for each of the parameters was performed by F test. Co-efficient of variation (CV%), Duncan’s Multiple Range Test (DMRT) and Least Significant Difference (LSD) test at 5% level of significance were done according to Gomez and co-warkers (Gomez and Gomez, 1984).
Bangladesh J. Sci. Ind. Res. 49(4), 227-232, 2014
Journal