21.09.2015 Views

CONTENTS

Contents of 41(2) 2013 - acharya ng ranga agricultural university

Contents of 41(2) 2013 - acharya ng ranga agricultural university

SHOW MORE
SHOW LESS
  • No tags were found...

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

SUBBA REDDY et al<br />

from the observations of Ravidas et al. (1992), Devi<br />

et al. (2007) and Kumar et al. (2007) in gladiolus.<br />

GA 3<br />

, NAA and BA at different concentrations<br />

significantly increased the mean spike length, number<br />

of florets and number of spikes per plant. These<br />

treatments were consistent and equally effective in<br />

increasing the leaf area almost during the entire crop<br />

growth period. The increase in leaf area thereby<br />

increased the assimilate synthesis, might have<br />

contributed to increase in spike length by these<br />

treatments. The increased spike length with GA 3<br />

might<br />

be due to rapid inter nodal elongation as a result of<br />

increased cell division and cell elongation in the<br />

intercalary meristem. As GA 3<br />

promotes vegetative<br />

growth and increases the photosynthetic and<br />

metabolic activities causing more transport and<br />

utilization of photosynthetic products this might have<br />

resulted in increased spike length. Mukhopadhyay<br />

and Banker (1986) also reported significant increase<br />

in spike length with GA 3<br />

in the gladiolus cv.<br />

Friendship. Similar results were also reported by<br />

Ravidas et al. (1992), Devi et al. (2007), Rajesh<br />

Bhalla and Ajay Kumar (2007). Flower inducing ability<br />

of BA was reported by several workers under in vitro<br />

as well as in vivo conditions. Induction of flowering<br />

may be due to its ability to alter the assimilate<br />

distribution (Ogawa and King, 1994) i.e. the theory of<br />

nutrient diversion (Sachs et al., 1979).<br />

TIBA recorded minimum spike length.<br />

Reduced spike length with TIBA might be due to its<br />

ability to inhibit polar transport of auxins in cell<br />

elongation and reduced photosynthetic efficiency.<br />

This view gets support from the observations of<br />

Ravidas et al. (1992) and Devi et al. (2007) in<br />

gladiolus. Number of florets per spike was maximum<br />

with GA 3<br />

, NAA and BA treatments. The lowest<br />

number of florets were recorded with TIBA. Increase<br />

in number of florets per spike with GA 3<br />

treatments in<br />

gladiolus have been reported by Rajesh Bhalla and<br />

Ajay Kumar (2007), Dataram et al. (2001) and<br />

PranavRana et al. (2005), who obtained the highest<br />

number of florets per spike by application of GA 3<br />

at<br />

100 ppm. NAA treatments resulted in production of<br />

maximum number of florets per spike which might<br />

be due to short inter nodel length. The lowest number<br />

of florets per spike with TIBA might be due to reduced<br />

plant height and spike length. Devi et al. (2007) also<br />

reported similar results while investigating with NAA<br />

and TIBA in gladiolus.<br />

Results from the present study indicated that<br />

the number of replacement corms per mother corm<br />

was significantly highest in GA 3<br />

followed by BA and<br />

NAA. PranavRana et al. (2005) reported similar<br />

results with GA 3<br />

treatments (100,250 and 500 ppm)<br />

in gladiolus. Singh et al. (2002) also noticed highest<br />

number of corms per plant by with GA 3<br />

followed by<br />

NAA at 200 ppm and BA at 100 ppm treatments in<br />

gladiolus. TIBA recorded the lowest number of<br />

replacement corms per mother corm. Devi et al.<br />

(2007) also reported similar results with GA 3<br />

, NAA<br />

and TIBA in gladiolus. Gladiolus has two sources<br />

for planting viz. corm and cormel which can serve as<br />

reserve food material in the initial stages, and<br />

photosynthesizing leaves in later stages. Likewise it<br />

has two competing sinks,viz., flower spike and the<br />

developing corm and cormels. Plant growth regulators<br />

in all the concentrations recorded maximum number<br />

of replacement corms, cormels and propagation<br />

coefficient. They might have promoted the sink<br />

activity of developing corm and cormels at the<br />

expense of flower spike, which may be the reason<br />

for increase in number of corms and cormels. Similar<br />

results were also observed by Tawar et al. (2007) in<br />

gladiolus. The increase in size and weight of corms<br />

with the application of plant growth regulators could<br />

be attributed to the ability to increase the number of<br />

leaves which in turn increased the photosynthesis<br />

and photosynthetic assimilates. These assimilates<br />

were transported to the daughter corms, thereby,<br />

increasing their size and weight. Supportively, lowest<br />

values for corm weight were recorded with control.<br />

Similar results of increase in size and weight of<br />

gladiolus corms have been reported by Maurya and<br />

Nagda (2002), Umarao et al. (2007 b) and Vijay Kumar<br />

and Singh (2008). The data on number and weight of<br />

cormels per corm revealed that both the parameters<br />

differed significantly due to plant growth regulator<br />

treatments. Among the plant growth regulator<br />

treatments, more number and maximum weight of<br />

cormels per corm were recorded with BA, followed<br />

by TIBA , GA 3<br />

and NAA. Tawar et al.(2007) and<br />

Havale et al. (2008) have reported that BA 50 ppm<br />

recorded the highest values for number of corms and<br />

cormels, weight of corms and cormels. Maximum<br />

number of cormels and weight of cormels was with<br />

12

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!