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