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Articles by Md. Sarwar Jahan
Total Records ( 2 ) for Md. Sarwar Jahan
  Mohammed Saifuddin , Mohammad Moneruzzaman Khandaker , Md. Sarwar Jahan , Nashriyah Binti Mat and A.B.M. Sharif Hossain
  Growth regulator is an important factor to enlarge the flower size in the floriculture industry. Flower growers have a lot of interest in making flower enlargement and shorten longevity to harvest flower earlier and to make it marketable soon. Gibberellic Acid (GA3) and aluminium sulphate Al2(SO4)3 play significant roles in flower enlargement and development. Hibiscus sp. was used in this experiment. The branches were dripped with the respective chemical [GA3 and Al2(SO4)3 100ppm] at 3 days intervals for 3 weeks. It had been shown that the 100 ppm GA3 played major role in developing a bigger size of the flower, production of more leaves, shorter longevity of flower, quicker bloom and greater size and weight of the flower as compared to the Al2(SO4)3 and control. Chlorophyll content (represented by SPAD value) and fluorescence were higher in GA3 treated branch than in aluminium sulphate treated branch and control. The quantum yield (Fv/Fm) was maximal in GA3 treated branch. The aluminium sulphate treated branch also showed the similar results but the longevity of the flower had the longer duration in aluminium sulphate treated branch than in GA3 but shorter than control. The results showed that these two chemicals [GA3 and Al2(SO4)3 100ppm] using dripping technique instead of spray were effective for the enlargement of flower size and shorten the flower longevity with less chemical cost and quantity of chemicals without hazarding the environment instead of spray . In addition, it improved the weight and increased the blooming rate and could be acceptable to the flower growers easily and could be harvested for commercial purposes earlier.
  Md. Moniruzzaman Sarker , Badrun Nesa and Md. Sarwar Jahan
  The egg type of Lymnaea acuminata was determined as iso-lecithal and the cleavage is spirally holoblastic type. The development of L. acuminata was observed in details. Uncleaved zygote just after laying was found to contain a relatively yolk-free zone, the animal pole and the yolk-rich region, the vegetal pole. No polar bodies were present in eggs examined immediately after they had been laid. The first polar lobe and polar body were extruded out from the zygote within 15-25 min. These were reabsorbed after 12-15 min. The formation of the second polar lobe was followed within the next 48 min. The first cleavage division occurred about 115-130 min after the formation and re-absorption of the second polar lobe, retaining for 7-10 min. The 2-celled embryos underwent the second equal division of cleavage the within next hour and the embryos reached the 4-cell stage. At the end of the 5th h, the 4-celled embryos underwent the third cleavage and the cleavage was horizontal (i.e., equatorial). At the end of the 9th h, the embryos at the 8-celled stage reached the 16-celled stage by the 4th cleavage. The 4th spirally cleaved embryos usually underwent fifth and sixth cleavages within 24-26 and 27-29 h of incubation, respectively. After 2-3 days of incubation, the developing embryos attained the trochophore stage. At the beginning of the 4th day of incubation, embryos became slightly elongated, curved foot muscle and shell gland were developed through the extension of velum and the embryos turned into the early veliger. At the beginning of the seventh day, the miniature snail possessed all the structures found in a newly hatched individual. Interaction between water physico-chemical parameters and some breeding parameters have been observed.
 
 
 
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