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Chapter V DISCUSSION The results obtained during the present investigation entitled, “Integrated Pest Management in Okra, Abelmoschus esculentus (L.) Moench” are discussed hereunder: 5.1 Insect-pests associated with okra crop For evolving an effective pest management strategy, it is imperative to know the insect-pest complex attacking a crop in a particular agro-climatic zone. Surveillance studies conducted on okra at Palampur revealed 18 different pests’ species belonging to 6 orders and 12 families associated with A. esculentus (var. Pusa Sawani) from June to September (Table 4.1). At Kachhiari (Kangra), 19 different pests’ species belon ging to 6 orders and 12 families were associated with okra crop from May to September (Table 4.2). At both the locations, Nodostoma spp. and Popillia spp. were identified as new insects of okra from the state. Nodostoma spp. were found to attack both foliage and flowers whereas Popillia spp. attacked flowers only although both these insects were rated as minor pests. Earlier Butani and Verma (1976) had reported as many as 30 insect and non-insect pests attacking okra crop. Dhamdhere et al. (1984) have listed 13 pests attacking okra at various stages of crop growth at Gwalior in Madhya Pradesh. Eight species of insects were reported to feed on okra at

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Chapter V

DISCUSSION

The results obtained during the present investigation entitled,

“Integrated Pest Management in Okra, Abelmoschus esculentus (L.) Moench”

are discussed hereunder:

5.1 Insect-pests associated with okra crop

For evolving an effective pest management strategy, it is

imperative to know the insect-pest complex attacking a crop in a particular

agro-climatic zone. Surveillance studies conducted on okra at Palampur

revealed 18 different pests’ species belonging to 6 orders and 12 families

associated with A. esculentus (var. Pusa Sawani) from June to September

(Table 4.1). At Kachhiari (Kangra), 19 different pests’ species belonging to 6

orders and 12 families were associated with okra crop from May to

September (Table 4.2). At both the locations, Nodostoma spp. and Popillia

spp. were identified as new insects of okra from the state. Nodostoma spp.

were found to attack both foliage and flowers whereas Popillia spp. attacked

flowers only although both these insects were rated as minor pests.

Earlier Butani and Verma (1976) had reported as many as 30 insect

and non-insect pests attacking okra crop. Dhamdhere et al. (1984) have

listed 13 pests attacking okra at various stages of crop growth at Gwalior in

Madhya Pradesh. Eight species of insects were reported to feed on okra at

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182

Raipur (Chhattisgarh) by Dubey et al. (1999). Our results are in close

consonance with Nath (1992) who reported 21 species of insects-pests

associated with okra crop at Solan, Himachal Pradesh and Singh and Joshi

(2004) who observed 15 pests associated with okra crop in Paonta valley of

Himachal Pradesh.

During the present investigation, the severity of pests was noticed

from June to September at both the locations. A number of workers have

also observed that the pests of okra are more serious from June to August

i.e. during warm and rainy season (Kashyap and Verma, 1982; Mahmood et

al., 1988; Kandoria et al., 1989).

The present research revealed that out of 18 pest species recorded

on okra at Palampur, 4 were observed to cause major damage to crop.

These included jassid, A. biguttula biguttula, aphid, A. gossypii, blister

beetle, M. pustulata and leafroller, S. derogata. At Kachhiari, in addition to

these pests, shoot and fruit borer, E. vittella was also observed as the major

pest of okra.

A. biguttula biguttula and E. vittella have already been recognized

as most serious pests of okra crop in different parts of country by many

researchers (Mote, 1977; Radke and Undirwade, 1981; Dhamdhere et al.,

1984; Gajbhiye et al., 1985; Chaudhary and Dadheech, 1989; Jamwal and

Kandoria, 1990; Kadam and Khaire, 1995; Bhagat and Bhat, 1999; Dubey et

al., 1999; Gogoi and Dutta, 2000; Mandal et al., 2006c, Gupta et al., 2007;

Singh, 2007; Singh et al., 2007).

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The current findings also find favour with Nath (1992) who

reported A. biguttula biguttula as major pest of okra from Solan valley of

Himachal Pradesh. Likewise, Bhatia and Gupta (2003) reported A. biguttula

biguttula as most serious pest of okra in Himachal Pradesh. The severity of

this pest on okra has also been described by Singh and Joshi (2004) from

Paonta valley of Himachal Pradesh and Kumar and Pathania (2006) from Una

in Himachal Pradesh.

A. gossypii has previously been reported to cause considerable

damage to okra crop in different parts of the country (Chaudhary and

Dadheech, 1989; Kandoria et al., 1989; Jamwal and Kandoria, 1990;

Devasthali and Saran, 1997; Patel et al., 1997a).

M. pustulata found as the major pest in current study has been

earlier observed feeding on floral parts of okra plant by Sharma et al.

(1964), Dhamdhere et al. (1984) and Sangha and Mavi (1995). The serious

infestation of blister beetle, M. phalerata on okra at Manipur has been

mentioned by Barwal and Rao (1988). Under mid hill conditions of Himachal

Pradesh, blister beetle has been reportedly observed attacking okra flowers

and thus lowering the yield (Kakar and Dogra, 1988; Anonymous, 2005b).

Even Nath (1992) observed Mylabris spp. to be causing principal damage to

okra in Solan valley of Himachal Pradesh. Sharma (2004) reported 4 species

of Mylabris associated with okra crop.

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However, Singh and Joshi (2004) mentioned aphids and blister

beetle as minor pests of okra. This can be attributed to the difference in

weather conditions which leads to variation in intensity of damage caused by

a pest from one region to another. In addition to these pests, S. derogata

too caused substantial damage to okra crop in the current investigation. The

damage by S. derogata to okra crop has formerly been cited by Dhamdhere

et al. (1984), Ghosh et al. (1999) and Singh and Joshi (2004).

A deep insight into the insect-pests associated with okra crop at

two locations revealed that in summer, less incidence of different pests was

observed (except E. vittella) as compared to the rainy months possibly

because of high temperature and low humidity prevalent in summers. This

view is supported by Sardana and Verma (1986) who based on their study

on cowpea concluded that in summer, low humidity and high temperature

are important factors in keeping insect population density at a low level in

comparison to rainy season.

In the current study, E. vittella was observed causing substantial

damage to okra fruits only at Kachhiari while at Palampur, it was present in

low numbers. This could be ascribed to the fact that at Kachhiari, the crop

was sown in the month of April and harvested in August/ September, thus

experiencing both summer and rainy seasons, whereas, at Palampur, the

crop was sown in end of May or beginning of June, which resulted in main

fruit bearing period during rainy season. Due to heavy rainfall in July-August

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at Palampur, the pest was unable to multiply and thus remained in lower

proportion. Further, higher temperature and lower humidity prevailing at

Kachhiari during initial stages of fruit setting were found quite suitable for

the development of the pest.

Madav and Dumbre (1985) detected no incidence of shoot and fruit

borer on okra throughout the kharif season in Maharashtra. Even Singh and

Brar (1994) reported from Ludhiana (Punjab) that the late sown crop of okra

(in July) revealed quite low infestation of E. vittella. The adverse effect of

high relative humidity (> 60%) and rainfall (> 20 mm/week) on E. vittella in

okra has been previously quoted (Kadam and Khaire, 1995).

5.2 Seasonal incidence/population build-up of major insect-pests on okra crop

The period of commencement of pest activity is known to fluctuate

depending on the prevalence of environmental conditions and availability of

suitable hosts.

5.2.1 Cotton jassid, A. biguttula biguttula

Appearance of jassids on okra was first noticed in the fields at

Palampur during 1st week of July during the two seasons whereas, at

Kachhiari, the pest was first seen in 4 th week of May during 2005 and 3rd

week of May during 2006 (Tables 4.3 – 4.4). The early appearance of the

pest at Kachhiari was probably due to early sowing of the crop in the month

of April as compared to Palampur (May/June).

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The population, after attaining an increasing trend through the

months of July and August with a population range of 2.25-46.20 jassids per

3 leaves at Palampur and 0.60-51.02 jassids per 3 leaves at Kachhiari

varying through the two seasons declined towards the end of crop growth

period but did not cease completely. These results are in agreement with

Patel et al. (1997a) who also observed that the jassid population on okra

amplified during the monsoons. The present findings are broadly in

corroboration with the research results of few workers (Mahmood et al.,

1990; Anonymous, 2005a) who observed the emergence of jassids on okra

in June-July, which remained active till the end of crop growth.

The existing results are also supported by those of Patel et al.

(1997a) who observed that the period of incidence of A. biguttula biguttula

lasted from July to September on okra under Gujarat conditions. Earlier also,

increased population of jassids on okra has been reported during the months

of July to September by Jayaraj and Basheer (1964), Uthamasamy et al.

(1973) and Uthamasamy (1988). Higher population of okra jassids in rainy

season as compared to summer season witnessed during the present study

get support from reports by Mohan et al. (1983) and Mishra and Senapati

(2003).

The peak of jassid population was observed in 3 rd to 4th week of

August at Palampur (45.86 and 46.20/3 leaves) and 4 th week of July to 1st

week of August at Kachhiari (39.21 and 51.02/3 leaves) during the two

seasons. Similarly, highest population of 18.00 jassids per okra leaf (Bhat,

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1999) and 10.34 jassids per okra leaf (Anonymous, 2005a) has been

observed in the last week of August at Jammu and Varanasi, respectively,

thus justifying the present findings. On the other hand, Krishnananda (1973)

and Balasubramaniam et al. (1977) reported a rise in the population of A.

biguttula biguttula during November-December. The difference in peak

activity period could be attributed to variation in weather conditions

prevailing over a particular place, the cropping season, time of sowing and

variety of crop grown.

The peak of jassid population was observed when the

meteorological conditions were 27.4-29.7oC (maximum temperature), 18.8-

25.3oC (minimum temperature), 75-80 per cent (relative humidity), 5.9-7.5

hours (bright sunshine hours) and 64.4-115.0 mm (total rainfall). The

meteorological range prevalent during the peak activity in the present

investigation has been reported to be favourable for the development of this

pest by earlier workers also.

Murugesan (1985) and Gupta et al. (1997) found peak population

of jassid when the minimum and maximum temperature ranged between

24.8 to 32.6oC. Further, Gupta et al. (1997) found relative humidity of 78

per cent conducive for multiplication of jassids which is in close harmony to

that found in the present study. Singh and Sekhon (1998) also substantiate

the present findings by reporting mean temperature of 30oC coupled with

less than 8.6 hours of bright sunshine (preferably 5 hours/day) favourable

for increase in jassid numbers.

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5.2.2 Cotton aphid, A. gossypii

At Palampur, the aphid activity commenced in 1st week of July

whereas at Kachhiari, it was evident in last week of June during both the

seasons. The population witnessed an increasing trend throughout the

months of July, August and September at Palampur and Kachhiari,

diminished a bit towards the end of crop maturity but was still present in

ample numbers at the time of final harvest (Tables 4.6-4.7). In the present

study, negligible incidence of aphids was observed in the month of June at

Kachhiari which augmented on the onset of monsoon. Kandoria et al. (1989)

also reported reduced population of aphids on okra during the summer

months (May-June) because of high temperature prevalent during that

period.

The existing results fairly match with those of Jamwal and

Kandoria (1990) who noticed the activity of A. gossypii on okra from 4th

week of July to 3rd week of October. In the present study, aphid population

sustained all throughout the cropping seasons and was present in substantial

numbers even towards the end of crop growth. Similar observations were

made by Ghosh et al. (1999) while studying seasonal incidence of aphids on

okra at Pundibari (West Bengal). On the contrary, aphids were most active

on okra during September-October in Punjab (Kandoria et al., 1989). The

variation in seasonal incidence is due to prevailing weather conditions which

differ from one region to other.

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At Palampur, peak aphid population was observed in 2nd to 3rd

week of August (85.27 and 94.65/3 leaves) whereas, at Kachhiari, it was

maximum during 2nd to 4th week of July (54.75 and 68.25/3 leaves). These

results broadly match with Ghosh et al. (1999) who viewed initiation of A.

gossypii activity on okra in mid June which reached in peak in the last week

of July and also with Al Eryan et al. (2001) who noticed appearance of

aphids on okra in the month of July which reached its peak in late August.

During the present investigation, peak population of aphid (A.

gossypii) was observed when mean maximum temperature ranged between

25.1-28.3oC, mean minimum temperature ranged between 19.2-25.4oC,

mean relative humidity ranged between 85-89 per cent, mean bright

sunshine ranged between 2.5-3.1 hours with total rainfall of 100.4-212.5

mm.

The present results regarding the favourable meteorological range

for A. gossypii is in harmony with the findings of Murugesan (1985) who

reported humid weather conditions highly favourable for cotton aphid. These

findings also find favour with Dhamdhere et al. (1995) who observed that

moderate temperature (27.3-28.2oC) and high humidity (73 %) favoured

build-up of A. gossypii on brinjal at Gwalior in Madhya Pradesh. Further,

Gupta et al. (1997) based on their two year study at Harda in Madhya

Pradesh found moderate range of minimum and maximum temperature

(24.8-30.1oC), high humidity (87-89 %) and drizzling rainy days quite

conducive for rapid build-up of aphid population on cotton, thus backing up

the current results.

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Critical appraisal of jassid and aphid incidence in relation to

weather parameters on okra in the present research indicated that the jassid

multiplication was favoured by higher maximum temperature (27.4-29.7oC)

and lower relative humidity (75-80%) as compared to that of aphid

population which was favoured by comparatively lower maximum

temperature (25.1-28.3oC) and higher relative humidity (85-89%). Similar

observations on the incidence of jassids and aphids were made by Gupta et

al. (1997) on cotton crop in Madhya Pradesh. They reported that higher

maximum temperature (32.6oC) and lower relative humidity (78%) were

conducive for the multiplication of A. biguttula biguttula whereas, lower

maximum temperature (26.1-30.1oC) and higher relative humidity (87%)

were found favourable for rapid build up of A. gossypii population.

Prevalence of higher humidity at Palampur as compared to

Kachhiari also explains the presence of higher aphid population at Palampur

during the current investigation. Although high rainfall was received during

the study period even then the aphids were present in considerable

numbers. This could be because of the fact that aphids have developed

several modes of reproduction such as viviparity, paedogenesis,

parthenogenesis etc. for their survival as has been mentioned by Dhaliwal

(2006).

5.2.3 Shoot and fruit borer, E. vittella

The appearance of E. vittella on okra fields was first noticed in 3rd

to 4th week of May at Kachhiari during the two seasons. A low incidence on

shoots varying between 0.82-2.24 per cent was observed initially for two

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weeks. As soon as the fruit setting started, the pest started infesting fruits

and by 1st week of June and thereafter, no damage on shoots was observed

(Table 4.9). The pest continued infesting fruits till 2nd week of July to 1st

week of August varying between 1.23-35.85 per cent and the larval

population varied between 0.37 to 2.35 per fruit during the two seasons.

Ambekar et al. (2000a) also observed negligible incidence of E.

vittella on okra shoots at Pune in Maharashtra. Analogously, Mandal et al.

(2006b) reported lower damage of shoot and fruit borer on okra shoots

varying between 0.3 to 3.46 per cent at Samastipur (Bihar). They also

observed that after fruit setting, there was no damage on shoots and the

pest shifted its activity exclusively on fruits, which corroborates the present

results.

Varying levels of fruit damage by E. vittella on okra crop ranging

between 32.1-100.0 per cent have been reported by various workers (Radke

and Undirwade, 1981; Dhawan and Sidhu, 1984; Madav and Dumbre, 1985;

Chaudhary and Dadheech, 1989; Kadam and Khaire, 1995; Gupta et al.,

1998; Mathur et al., 1998; Mandal et al., 2006b) depending on prevailing

agro-climatic conditions in their respective areas of study.

Peak fruit infestation (29.64 and 35.85%) during the current study

was noticed during 3rd to 4th week of June which in the following weeks

declined and ceased completely by 3rd week of July to 2nd week of August

because of heavy rainfall received during the later period. Almost similar

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pattern of fruit infestation on okra was observed by Mote (1977) at Rahuri in

Maharashtra, according to whom, E. vittella infestation started as soon as

the fruits set (6 weeks after germination), attained a maximum 3-4 weeks

later during summer after which it declined.

The peak activity of the pest noticed during the month of June is in

accordance with Shukla et al. (1997) from Jabalpur (Madhya Pradesh) who

reported peak fruit damage by E. vittella in 1st fortnight of June. The peak

period of activity of E. vittella in India has been known to vary from region

to region i.e. late October in Punjab (Dhawan and Sidhu, 1984), November-

December in Maharashtra (Kadam and Khaire, 1995), 4 th week of July in

Bihar (Gupta et al., 1998), 2nd fortnight of August in West Bengal (Ghosh et

al., 1999), 4th week of September in Gujarat (Zala et al., 1999) and 4th week

of October in Uttar Pradesh (Anonymous, 2005a). The variation in peak

activity may be ascribed to difference in meteorological conditions prevailing

over a particular place, cropping season, time of sowing and variety of crop

grown.

More severity of E. vittella on okra crop sown in the summer

months as compared to one sown in rainy season was noticed by Mohan et

al. (1983) and Kumar and Urs (1988). Related observations were also made

by Dhawan and Sidhu (1984) who reported from Punjab that maximum

damage to okra fruits by E. vittella was evident in spring crop and that

heavy rainfall adversely affected population build-up of this pest. Lower

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incidence of E. vittella because of heavy rainfall has also been documented

by Kadam and Khaire (1995) at Ahmednagar, Maharashtra. They observed

high damage by E. vittella during summer months and low damage during

rainy months.

The lower damage recorded during the rainy season could be

because of dislodgement of eggs and neonate larvae of shoot and fruit borer

by the rains as well as the prevalence of high humidity. According to Kadam

and Khaire (1995), the adverse effect of high relative humidity (> 60%) and

rainfall (>20 mm/week) could form a component of eco-friendly

management of Earias species. Further, they reported that infestation could

be reduced to a greater extent by growing okras during the rainy season.

The mean meteorological conditions present during the peak pest

activity were maximum temperature of 34.6-35.3oC, minimum temperature

of 21.9-26.9oC, relative humidity of 36-47 per cent and 12.1-31.2 mm of

total rainfall. These observations are substantiated by Radke and Undirwade

(1981) who found peak infestation on okra fruits (100%) by Earias spp.

when average weekly maximum temperature was 30.8oC, minimum

temperature was 21.1oC and relative humidity was 49 per cent. In the past,

a number of workers have reported temperature of about 35oC to be

congenial for the development of this pest which supports the present

findings (Ahmad and Ullah, 1941; Pradhan and Menon, 1945; Kashyap and

Verma, 1982).

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5.2.4 Blister beetle, Mylabris spp.

Seasonal incidence studies on okra revealed that Mylabris beetles

emerged in okra fields in 4th week of July to 1st week of August at Palampur

and 1st to 3rd week of July at Kachhiari (Tables 4.11-4.12). These results are

in corroboration with Sharma et al. (1964) who reported that the blister

beetles appeared in July in Himachal Pradesh on various crops including

okra. Similar observations were made by Sangha and Mavi (1995) from

Ludhiana (Punjab) who reported that M. pustulata appeared in 2nd fortnight

of July on okra.

The peak activity of the pest was observed in 3 rd week of August to

1st week of September at Palampur with maximum population of 24.5-29.6

beetles per 10 plants and maximum flower damage of 26.90-31.15 per cent.

At Kachhiari, peak activity was observed in 2nd to 3rd week of August with

maximum beetle population varying between 31.8-35.6 per 10 plants and

flower damage varying from 32.69-38.52 per cent. A declining trend was

then set in and low beetle incidence was observed in 2nd to 4th week of

September at Palampur and 4th week of August to 1st week of September at

Kachhiari.

During the present study, maximum beetle population and flower

damage were viewed when the mean meteorological conditions of 27.7-

29.1oC (maximum temperature), 20.2-25.8oC (minimum temperature), 75-79

per cent (relative humidity), 7.1-7.9 hours (bright sunshine) and 37.8-80.5

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mm (total rainfall) were prevalent. These findings are supported by reports

of Sharma et al. (1964) from Himachal Pradesh and Sangha and Mavi (1995)

from Punjab who observed peak activity of blister beetle on okra during the

month of August. The present results also find favour with Dutta and Singh

(1989) who reported that M. phalerata population peaked in August at the

time of flowering in pigeon-pea in Uttar Pradesh.

The favourable range of meteorological parameters for blister

beetle multiplication observed during the present study is validated by

Sardana and Verma (1986). They found that blister beetle, M. pustulata

showed its peak on cowpea between last week of August to 1st week of

September at Delhi when maximum temperature varied between 25-32oC

and relative humidity varied between 60-92 per cent with total rainfall

ranging from 20 to 90 mm. The existing findings are also in line with

Bhardwaj (1996) who reported that on black gram, peak blister beetle

population was noticed in 4th week of July to 1st week of September in

Himachal Pradesh when mean temperature and relative humidity were 23.3-

25.0oC and 72-85 per cent, respectively, with total rainfall of 16.2 mm-273.4

mm.

5.2.5 Cotton leafroller, S. derogata

The present studies revealed that the leafroller activity was first

evidenced on okra plants during 2nd to 4th week of July at Palampur while at

Kachhiari, it was first observed in last week of June to 1st week of July

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(Table 4.14 - 4.15). The highest incidence of S. derogata on okra was

observed in 1st to 3rd week of August at Palampur with maximum larval

population of 34.7-38.1 per 10 plants as well as maximum rolled leaf

infestation of 26.97-29.21 per cent. At Kachhiari, maximum population of

33.8-36.3 larvae per 10 plants and maximum rolled leaf infestation of 25.70-

27.16 per cent were observed during last week of July during both the

seasons. During the peak activity, the meteorological conditions prevalent at

the two locations were mean maximum temperature in the range of 25.8-

28.4oC, mean minimum temperature in the range of 20.1-25.4oC, mean

relative humidity in the range of 80-89 per cent, mean bright sunshine in the

range of 2.3-3.1 hours and total rainfall of 100.4-211.2 mm.

Literature regarding the seasonal incidence of S. derogata on okra

is meagre. However, Lal and Singh (1951) reported low temperature and

high humidity coupled with rainy days favourable for the development of leaf

roller which is in accordance with the present results. These findings are also

in consonance with Ghosh et al. (1999) who observed that population of

okra leafroller initiated in 1st week of July at Pundibari (West Bengal) and

higher population (0.80 larva/plant) was maintained till August which

decreased gradually thereafter. They noticed maximum population of the

pest at mean maximum temperature of 29.3oC, mean minimum temperature

of 24.0oC and mean relative humidity of 90-97 per cent, thereby broadly

validating the present findings.

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5.3 Correlation of abiotic factors with population build- up of major insect-pests on okra

5.3.1. Cotton jassid, A. biguttula biguttula

At Palampur during 2005, rainfall exhibited a significant negative

outcome while bright sunshine hours showed a significant positive

relationship with population count of the pest. During 2006, none of the

weather factors showed a significant correlation with pest population (Table

4.5). Interestingly, at Kachhiari, maximum temperature negatively but non-

significantly influenced pest activity while relative humidity had a significant

positive impact on jassid population during both the years of study. Besides,

minimum temperature influenced pest activity significantly and positively at

Kachhiari during 2006 (Table 4.5).

The present results are in line with those of Reddy et al. (1983),

Dhuri et al. (1984) and Faleiro and Singh (1985) who observed positive

correlation of minimum temperature and relative humidity with jassid

population on a variety of crops. The positive correlation of A. biguttula

biguttula with relative humidity is in conformity with Jayaraj and Basheer

(1964) who observed humid season quite conducive for population build-up

of this pest.

The positive correlation of the jassid density with minimum

temperature is in accordance with Mahmood et al. (1990). These workers,

however, contrary to the present results, observed no significant

contribution of relative humidity and rainfall in influencing the pest numbers.

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This is because of the difference in climatic conditions which vary from one

place to another. The significant negative correlation of jassid count with

rainfall at Palampur (2005) could be attributed to comparatively higher and

almost incessant rainfall received during 2005 as compared to 2006 which

would have led to the splashing of mud on to the underside of leaves,

resulting in mortality of jassids. Similar reports are available from Sudan

where good suppression of jassid population on cotton was brought about by

heavy rainfall (Hanna, 1970).

The significant negative correlation of jassid count with maximum

temperature and positive correlation with bright sunshine has earlier been

illustrated by Patel et al. (1997a) on okra. Likewise, positive correlation of

population count of jassids with average relative humidity has been

previously mentioned by Sharma and Sharma (1997). Bhat (1999) while

correlating A. biguttula biguttula population and abiotic factors at Jammu on

okra revealed that the population was negatively correlated with rainfall

while significantly and positively correlated with bright sunshine hours which

is in complete agreement with the present results.

The wide variation in correlation coefficients obtained between

abiotic factors and jassid population at Palampur and Kachhiari could be

ascribed to the fact that at Kachhiari, the crop passed through the hot

summer months as well as rainy season whereas, at Palampur, the crop

underwent through the rainy season only, thus the pest experienced wide

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variation in maximum and minimum temperature, relative humidity and

rainfall at the two locations but multiplied only when the favourable range of

meteorological conditions were available. Dhaliwal and Arora (2003) also

mentioned that the degree of influence of environmental factors determines

the magnitude of increase or decrease in numbers of a pest population and

that every insect species multiplies only when the favourable range of

meteorological conditions are approached.

5.3.2 Cotton aphid, A. gossypii

The population of aphids on okra illustrated a positive significant

correlation with relative humidity at both the locations during both the years

(Table 4.8). In addition, pest numbers were significantly and negatively

correlated with maximum temperature at Palampur during 2005 and at

Kachhiari during both the seasons. Conversely, minimum temperature

correlated positively and significantly with aphid density at Kachhiari during

2006.

The present results are in concordance with Feleiro et al. (1990)

who revealed that on cowpea, population of A. gossypii was negatively

correlated with maximum temperature and sunshine hours and positively

correlated with minimum temperature and relative humidity in Delhi.

Likewise Gupta et al. (1997) observed significant positive relationship

between aphid density and relative humidity and significant negative

relationship with maximum temperature on cotton in Madhya Pradesh. These

results are also in tune with Ghosh et al. (1999) who reported negative and

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non-significant correlation of aphid count with maximum temperature and

non significant and positive correlation with relative humidity on okra in

West Bengal.

5.3.3 Shoot and fruit borer, E. vittella

At Kachhiari, maximum temperature exhibited a significant positive

correlation with fruit infestation as well as larval population during both the

seasons while relative humidity illustrated a significant negative relationship

with fruit infestation during 2005. Besides, rainfall had a significant negative

correlation with larval population during 2005 (Table 4.10). Radke and

Undirwade (1981) have also observed higher incidence of E. vittella on okra

with increase in temperature. The adverse effect of rainfall on population

build-up of E. vittella has been observed by Dhawan and Sidhu (1984) at

Ludhiana, Punjab.

The present correlation analysis is also supported by Kumar and

Urs (1988) from Bangalore and Zala et al. (1999) from Gujarat who noticed

that temperature had a positive and significant association with incidence of

E. vittella while relative humidity was negatively related with pest incidence.

Parallel results were obtained by Kadam and Khaire (1995) from Rahuri,

Maharashtra who observed a significant and negative correlation between

relative humidity, rainfall and E. vittella infestation on okra. Likewise, Bhat

(1999) viewed negative correlation of rainfall and fruit infestation by E.

vittella on okra in Jammu which is in close agreement with the present

findings.

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However, on the contrasting side, a significant negative correlation

between okra fruit infestation by E. vittella and maximum temperature while

significant positive relationship with total rainfall was analyzed by Gupta et

al. (1998) and Mandal et al. (2006b) in Bihar. This difference could be

ascribed to the variability in weather conditions from one place to another.

5.3.4 Blister beetle, Mylabris spp.

During 2005, at Palampur as well as Kachhiari, none of the

weather factors influenced beetle population as well as flower damage

significantly (Table 4.13). Nonetheless, during 2006 at Palampur, there was

a significant positive correlation between beetle population, flower damage

and maximum temperature. In addition, relative humidity had a significant

negative bearing while bright sunshine hours had a significant positive

bearing on flower damage at Palampur in 2006. Further, minimum

temperature exerted a significant negative impact on flower damage by

Mylabris spp. at Kachhiari during 2006.

There are no reports available on okra to validate the present

results. However, some reports are available in the literature pertaining to

the effect of weather factors on blister beetle population in pigeon-pea.

Sekhar (1991) reported that daily temperature and sunshine hours had a

significant positive effect while relative humidity showed a non-significant

negative correlation with blister beetle activity, which corroborates present

results. Identical reports are available from New Delhi in which, positive

correlation of M. pustulata population with maximum temperature and bright

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sunshine hours have been illustrated (Reddy et al., 2001). Even Sandal

(2007) reported a significant and positive correlation of Mylabris population

with maximum temperature on pigeon-pea at Palampur in Himachal Pradesh,

thus supporting present results.

5.3.5 Cotton leafroller, S. derogata

The present studies revealed that S. derogata larval population

positively and significantly correlated with relative humidity at Kachhiari

during both the crop seasons while at Palampur during 2006 only (Table

4.16). Contrastingly, bright sunshine hours exercised negative and

significant effect on larval population as well as per cent rolled leaf

infestation at Palampur during 2006. In addition at Kachhiari during 2006,

maximum temperature displayed a significant negative association with

larval population.

Low temperature and high humidity have earlier been found

favourable for the development of S. derogata on okra by Lal and Singh

(1951). The significant negative influence of bright sunshine hours on leaf

roller activity can be substantiated by the work of Lal and Singh (1951) and

Butani and Verma (1976) who have mentioned cloudy weather and rainy

days congenial for the activity of this pest. Ghosh et al. (1999) also support

the current findings by obtaining negative and non-significant correlation of

leafroller larval population with maximum temperature and positive and

significant correlation with minimum temperature and relative humidity on

okra at Pundibari (West Bengal).

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5.4 Screening of okra varieties/hybrids for resistance against major insect-pests Development and cultivation of resistant varieties to pests provides

a suitable and desirable means of pest management. The success of such

programme depends upon the extent of variability in the germplasm.

Further, in crops such as okra, frequent pickings, high operational cost and

residual effect of insecticides are the limiting factors for the management of

insect-pests through chemicals. Therefore, the most effective and

economical management of okra pests is the use of resistant varieties but a

variety resistant to a pest in one region may become susceptible in other

region. Hence, ten okra varieties/hybrids (including 3 recommended

commercial varieties for Himachal Pradesh) were evaluated for their relative

susceptibility against major insect-pests at two locations viz. Palampur and

Kachhiari.

5.4.1 Cotton jassid, A. biguttula biguttula

The mean jassid population (nymphs + adults) varied from 8.52 to

36.12 per 3 leaves on different varieties during the two seasons at two

locations (Table 4.17-4.19). Variety Tulsi (8.52-10.71 jassids/3 leaves) and

Varsha Uphar (8.83-11.93 jassids/3 leaves) showed lower population of the

pest at Palampur. At Kachhiari also, Tulsi revealed lowest jassid population

(11.33-11.61/3 leaves) while Varsha Uphar (14.74-15.25/3 leaves) was rated

as one having moderate population. Other varieties which recorded

moderate pest numbers at Palampur were Arka Anamika, Parbhani Kranti

and Panchaali while at Kachhiari, the same varieties were categorized in the

group of high population.

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The variation in susceptibility among varieties could be due to

certain inherited characters as well as due to variable environmental

conditions from region to region and year to year. These findings get

support from those of Kashyap and Verma (1986) who reported similar

reasons for difference in susceptibility among genotypes. The wide variation

with respect to rating of varieties at the two locations could be allotted to

the wide variation in overall pest pressure which was lower at Palampur as

compared to Kachhiari.

Variation in morphological characters as well as biochemical

components must have contributed to differential response of varieties

(Taylo and Bernardo, 1996; Dhaliwal and Arora, 2003) to jassids.

Uthamasamy et al. (1973) obtained a positive correlation of jassid incidence

with plant height and stem thickness in okra. It is known that the varieties

viz. Pusa Makhmali, P-8, Harbhajan and Parbhani Kranti are tall (Singh,

2007) and accordingly must have harboured more jassid population in the

current study. Teli and Dalaya (1981b) reported that Pusa Sawani showed

lower hair density (3.80/25mm2) on leaf lamina as compared to other

varieties and was more preferred for oviposition by jassids. It has also been

observed that okra varieties having more and longer hairs on the mid-rib and

leaf lamina are resistant to jassid (Uthamasamy, 1985; Singh, 1988; Singh

and Agarwal, 1988; Lal et al., 1997).

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Soft stem hair present in Parbhani Kranti, Pusa Sawani and P-8 and

lower hair density on mid veins of Pusa Sawani leaves (Mahal et al., 1993b;

Sharma and Arora 1993; Gill et al., 1997; Hooda et al., 1997; Dhankhar and

Mishra, 2001; Thakur et al., 2003) can partly explain higher jassid

population harboured by these varieties.

Even though Pusa Makhmali has hairy stem and leaves (Sharma

and Arora, 1993; Dhankhar and Mishra, 2001), it was reported as susceptible

variety in the present investigation. This could be because of the fact that

for an okra variety to be resistant to jassids, the complete complement of

hair characters viz. long, dense and erect are required as has been

mentioned by Singh and Taneja (1989) plus the composition of right amount

of different biochemicals, which could be lacking in this variety, thus proving

susceptible. Teli and Dalaya (1981b) too observed White Velvet variety of

okra as susceptible to jassid even though it had highest hair density

(9.30/25mm2) among the 6 varieties tested.

The existing findings are also supported by those of Bhat (1999)

who observed Varsha Uphar and Arka Anamika to be less preferred by

jassids (6-10/okra leaf) as compared to Shagun and Parbhani Kranti (15-

20/leaf). He has ascribed more trichome length (0.57-0.80 mm) and

trichome density (13.63-21.36/cm2) in less preferred varieties (Varsha

Uphar, Arka Anamika) responsible for providing resistance against jassids by

impeding feeding, oviposition and adult emergence.

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Among the different biochemical components, varieties of okra

having higher tannins, phenols, epicuticular waxes, silica and potassium and

lower moisture, proteins and total sugars in leaves have been reported to be

resistant to jassid (Singh, 1988; Singh and Agarwal, 1988, Singh and Taneja,

1989; Kaur et al., 1996). Comparatively lower proteins (12.81-13.21%),

moisture (64.15-69.22%) and sugar content present in leaves of Arka

Anamika and Varsha Uphar and more proteins (16.40-18.52%), moisture

(78.00-89.20%) and sugars in leaves of Parbhani Kranti, P-8, Pusa Sawani

and Shagun (Chavan et al., 1991; Reddy et al., 1997; Bhat, 1999) are

accountable for the relative resistance and susceptibility of these varieties.

The susceptibility of Pusa Makhmali and Harbhajan varieties to

okra jassids has been previously quoted in the literature (Sandhu et al.,

1974; Gill et al., 1997). The relatively low susceptibility of variety Varsha

Uphar to jassid noticed during the present investigation was also reported by

Dhankhar and Mishra (2001). Likewise, moderate susceptibility of Parbhani

Kranti (Bhat, 1999; Dubey et al., 1999) and higher susceptibility of Shagun

to A. biguttula biguttula (Bhat, 1999) have been earlier illustrated. High level

of susceptibility to jassid reported in Pusa Sawani is in consonance with the

work of Sandhu et al. (1974), Uthamasamy and Subramaniam (1980), Mahal

et al. (1993b), Gill et al., (1997), Hooda et al., (1997), Sharma and Sharma,

(1998) and Kumar and Singh (2002) who obtained similar results from their

respective areas of study.

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5.4.2 Cotton aphid, A. gossypii

The mean seasonal population of aphids on okra ranged from

18.96-70.54 individuals per 3 leaves on different varieties at the two

locations (Table 4.20-4.22). Among the different varieties, Tulsi (31.29-

39.44/3 leaves) and Varsha Uphar (35.81-43.94/3 leaves) showed moderate

level of aphid infestation on okra leaves at Palampur during the two seasons.

At Kachhiari, lower infestation by the pest was noticed on varieties Tulsi

(18.96-20.85/3 leaves), Varsha Uphar (21.15-24.61/3 leaves), Arka Anamika

(26.15-29.72/3 leaves) and Parbhani Kranti (25.93-30.08/3 leaves) while at

Palampur, the latter two varieties fall in the mean rating of high population.

This fluctuating trend, varying through seasons and locations is

ascribed to inherited characters of varieties as well as environmental

conditions. Ghosh et al. (1999) reported moderate level of infestation of A.

gossypii on Parbhani Kranti (14.64/leaf) and Arka Anamika (21.58/leaf)

which corroborate present results.

Certain morphological characters might have been responsible for

differential aphid attack. Roy (1990) mentioned thick okra leaves to be a

criterion for aphid resistance. Khan et al. (2000) reported that genotypes of

ashgourd having higher trichome density were least infested by A. gossypii

and thus provide a first line of defence in reducing aphid infestation. Lower

trichome density has been reported in leaves of Parbhani Kranti, Shagun and

Pusa Sawani (Teli and Dalaya, 1981b; Mahal et al., 1993b; Bhat, 1999)

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making these varieties more susceptible to aphids. Likewise, Varsha Uphar

and Arka Anamika exhibit higher trichome density and length (Bhat, 1999),

thus proving to be less preferable for aphids as noticed in the present

results.

According to Dhaliwal and Arora (2003), the stem tips of cotton

varieties tolerant to A. gossypii were nearly twice as stiff as those of

susceptible cultivars and they indicated difficulty for piercing proboscis into

hard stems of tolerant varieties as one of the main causes for non-

preference by aphids. Among the biochemical constituents, Du et al. (2004)

reported that high gossypol content in cotton genotypes had an antibiotic

effect on A. gossypii by reducing adult longevity and lowering fecundity.

Comparatively higher population of A. gossypii on all the okra

varieties at Palampur as compared to Kachhiari can be attributed to the

availability of more humid weather at Palampur, in comparison to Kachhiari

which was found highly conducive for aphid multiplication. The humid

weather has previously been found favourable for rapid build-up of aphid

population by Murugesan (1985) and Gupta et al. (1997).

5.4.3 Shoot and fruit borer, E. vittella

The pest was reported as major only at one location i.e. Kachhiari.

The mean per cent fruit infestation varied between 3.79 and 24.02 during

the two years on different varieties (Tables 4.23-4.24). Varieties were

grouped according to the mean rating given by Bhalla et al. (1989) for fruit

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infestation by E. vittella. Lowest fruit infestation (3.79-4.59%) was recorded

on Tulsi which was rated as resistant while a high level of fruit infestation

was recorded on Pusa Sawani (23.41-24.02%) during the two seasons which

was rated as susceptible. Other varieties viz. Varsha Uphar, Parbhani Kranti,

Arka Anamika, Panchaali and Harbhajan also revealed lower fruit damage by

E. vittella with respective mean per cent infestation of 6.65-7.41, 8.22-9.53,

11.80-11.94, 12.77-14.58 and 13.36-13.91 during the 2 seasons and were

categorized as moderately resistant.

High level of susceptibility to E. vittella reported in Pusa Sawani

variety in the present study has earlier been demonstrated by a number of

workers (Raut and Sonone, 1979; Kashyap and Verma, 1983; Madav and

Dumbre, 1985; Sharma and Dhankhar, 1989, Vyas and Patel, 1990; Vyas

and Patel, 1991). Kashyap and Verma (1983) recorded higher fruit

infestation (20%) on Pusa Makhmali variety, thus supporting the existing

findings. Sharma and Dhankhar (1989) viewed 13.42, 17.38 and 24.52 per

cent fruit infestation on P-8, Pusa Makhmali and Harbhajan, respectively,

which is in close agreement to that found (13.36- 21.71%) in the present

investigation. Similarly, Raj et al. (1993) observed 9.89 per cent fruit

infestation by E. vittella on Parbhani Kranti and 12.87 per cent on Harbhajan

at Jachh (Himachal Pradesh), which is in complete line to that noticed (8.22-

13.36%) in the current investigation.

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Earlier Bhat (1999) had rated Varsha Uphar as fairly resistant (6-

10% fruit infestation) while Shagun as highly susceptible (>20 % fruit

infestation) to E. vittella which is in tune to the present results. Moderate

level of resistance of Parbhani Kranti and Arka Anamika with respect to fruit

damage by borer in the present study is substantiated by the findings of

Ghosh et al. (1999) who revealed that Parbhani Kranti (9.05%) and Arka

Anamika (10.10%) had low fruit infestation by E. vittella.

According to Teli and Dalaya (1981a), varieties of okra having hard

skin with tough hairs were least susceptible to E. vittella attack. Certain

morphological characters such as increased hair density on leaf lamina was

related to fruit borer resistance in okra by Kumbhar et al. (1991). Sparse

pubescence present on fruits of Pusa Sawani and P-8 (Dhankhar and Mishra,

2001; Thakur et al., 2003) and spineless fruits of Harbhajan and Arka

Anamika (Sharma and Arora, 1993; Devdas et al., 1998) could be the cause

for more preference of these varieties to fruit borer. Bhat (1999) attributed

more thickness of fruit rind in Varsha Uphar (0.33-0.35mm) and higher

trichome density on fruits (23.66-29.33/cm2) and less rind thickness and

lower trichome density in Shagun responsible for imparting relative

resistance and susceptibility of these two varieties to E. vittella as has been

observed in the present study.

Certain biochemical constituents must have also served as

defensive mechanisms against E. vittella resulting in lower incidence of the

pest in less susceptible varieties. Higher sugar content (6.96-9.88%) and

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lower total fibre content (5.47-5.74%) in Pusa Sawani (Rao and Sulladmath,

1977) could be accountable for susceptibility of this variety to shoot and fruit

borer. Singh and Singh (1987) mentioned higher tannin content in fruit

pericarp of fruit borer tolerant okra genotypes than susceptible genotypes.

Likewise, lower proteins (11.95-12.52%), sugar (5.03-5.40%), moisture

content (88.16-88.23%), ascorbic acid (100-115 mg/100g dry fruit weight),

pH level (5.4-5.8) (Devdas et al., 1998; Bhat, 1999, Yadav et al., 2006) and

more fibre, tannin and potassium content in fruits of Varsha Uphar and Arka

Anamika (Bhat, 1999) must have been the parameters for comparatively

lower fruit infestation by E. vittella observed in these varieties.

The present results are however, opposite to those obtained by

Kashyap and Verma (1983) who observed low damage (< 10%) by fruit

borer on Harbhajan variety at Hisar and Raj et al. (1993) who reported less

incidence of fruit damage by E. vittella on Pusa Sawani (6.42%) at Jachh

(H.P.) as compared to Parbhani Kranti (9.81%) and Harbhajan (12.87%).

This could be allocated to the ecological differences, variation in climate and

date of sowing of crop from region to region.

5.4.4 Blister beetle, Mylabris spp.

The mean seasonal population of Mylabris beetles per 10 plants

varied between 3.80 to 24.13 and flower damage ranged between 4.45 to

24.05 per cent at the two locations on different varieties (Tables 4.25-4.27).

Least beetle count was observed on Varsha Uphar (3.80-3.93/10 plants) at

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Palampur with minimum flower damage of 4.45-5.14 per cent. At Kachhiari

also, same variety proved to be least susceptible with pest population of

4.20-4.80 beetles per 10 plants and flower damage varying from 5.04 to

5.67 per cent during the two seasons.

The highest population of beetles (14.60-24.13/10 plants) as well

as the maximum damage to flowers (17.15-24.05 per cent) were registered

by Pusa Sawani during the two years at both the locations. Other varieties

which experienced lower pest infestation were Tulsi, Arka Anamika and

Panchaali which revealed slight variations in their differential response to

pest attack at the two locations.

On all the varieties, the overall pressure of blister beetles was

lower during 2006 as compared to 2005 crop season at both the locations.

This could be explained partly on the basis of environmental conditions and

partly on the basis that during 2006, at both the locations, pulse crops such

as pigeon-pea and cowpea were grown in the adjoining fields and this pest,

being polyphagous, damaged these crops also besides attacking okra, which

reduced population of Mylabris beetles on okra.

Literature pertaining to blister beetle incidence on okra is scanty as

this pest has been reported minor in most of the earlier reports (Dhamdhere

et al., 1984; Singh and Joshi, 2004). However, according to Dent (2000),

glandless cotton varieties are more susceptible to blister beetles. Lale and

Sastawa (2000) evaluated 6 pearl-millet varieties viz. Ex-borno, Wame,

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Zongori, Gargasori, Mboderi and GB 8735 for their relative susceptibility to

Mylabris beetles in Nigeria and found significant differences among them

with respect to damage caused by the beetles as was observed in the

present investigation on okra.

5.4.5 Cotton leafroller, S. derogata

The mean larval population of leafroller varied from 7.33 to 28.13

per 10 plants on ten varieties during the two seasons at the two locations

(Tables 4.28-4.30). Variety Varsha Uphar showed lowest number of larvae at

both the locations varying between 9.80-12.60 per 10 okra plants at

Palampur and 7.33-9.73 per 10 plants at Kachhiari throughout the two

seasons. Tulsi also registered lower larval population i.e. 12.47-15.60 per 10

plants at Palampur and 9.00-11.20 per 10 plants at Kachhiari. Likewise, the

rolled leaf infestation was minimum in Varsha Uphar i.e. 5.28-7.64 per cent

at Palampur and 4.01-4.86 per cent at Kachhiari followed by Tulsi at both

the locations. At Palampur, Pusa Makhmali recorded highest larval

population of leafroller (25.53-28.13 per 10 plants) as well as maximum

rolled leaf infestation (18.29-19.89%) followed by Pusa Sawani. Reverse was

true at Kachhiari, where maximum larval population (22.47-25.73/10 plants)

and rolled leaf infestation (15.37-17.81%) were observed on Pusa Sawani

followed by Pusa Makhmali.

At Palampur, comparatively higher incidence of the pest was

apparent on all the varieties than Kachhiari. This could be credited to the

availability of more humidity and lower temperature at Palampur during the

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pest activity as compared to Kachhiari. Even Lal and Singh (1951) reported

that low temperature and high humidity coupled with number of rainy days

favour development of S. derogata. Other varieties which manifested low to

moderate infestation of leafroller were Arka Anamika, Parbhani Kranti and

Panchaali. Parallel results were obtained by Ghosh et al. (1999) who

reported moderate level of resistance in Arka Anamika and Parbhani Kranti

to S. derogata as compared to other varieties in West Bengal. There are no

other reports available in literature to confirm the present findings.

5.5 Marketable yield of okra varieties

Variety Tulsi registered highest yield at Palampur (67.47-72.10 q

ha-1) as well as at Kachhiari (87.72-93.03 q ha-1) and was significantly

superior to rest of the varieties. It was closely followed by Varsha Uphar

which recorded 62.56 to 84.04 q ha-1 yield at the two locations during the

two seasons. Other varieties which registered considerably higher yield at

both the locations were Arka Anamika, Panchaali, Parbhani Kranti and

Shagun. Lowest yield was however, obtained in Pusa Makhmali i.e. 29.45 to

31.49 q ha-1 at Palampur and 37.20 to 38.30 q ha-1 at Kachhiari (Table

4.31).

The variation in yield among the varieties could be accredited to

the genotypic variations, environmental difference and relative susceptibility

of different varieties to various insect-pests and diseases. Higher yield

obtained in all the varieties at Kachhiari as compared to Palampur could be

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because of the difference in climate and soil type at the two locations.

Further, at Kachhiari more number of pickings were carried out as the crop

was of longer duration (April-August/September) than Palampur, where the

crop was of relatively shorter duration (May/June-September).

In the present study, although Shagun recorded higher incidence

of almost all the major pests, yet it gave higher yield. This can be attributed

to the tolerance phenomenon and higher yield potential of this variety.

Analogous observations were made by Shukla et al. (1998) at Jabalpur

(Madhya Pradesh) who described that even though varieties Ankur 35 and

Parbhani Kranti of okra registered significantly higher damage by E. vittella,

yet produced higher fruit yields.

Sharma and Dhankhar (1989) recorded lower yield from Harbhajan

and Pusa Makhmali as compared to other varieties at Hisar, thus

substantiating the current findings. Likewise, Raj et al. (1993) from Himachal

Pradesh obtained lower yield from Pusa Sawani variety as compared to other

varieties which is in agreement to the present results and ascribed the

severity of mosaic on Pusa Sawani variety responsible for its lower yield.

The data regarding higher yield of Varsha Uphar as compared to

Arka Anamika, Pusa Makhmali, Parbhani Kranti, Shagun and Harbhajan

recorded during the current investigation is in consonance with a study

carried out at Dhaulakuan, Himachal Pradesh (Anonymous, 1999). At

Hamirpur (Himachal Pradesh), Arka Anamika recorded highest yield followed

by Tulsi, Varsha Uphar, Shagun, Panchaali, Parbhani Kranti, Harbhajan and

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P-8 (Anonymous, 2004a) which is in close harmony to the existing results

although comparatively lower yield was recorded on all the varieties in the

present study. This could be because of the difference in time of sowing,

variety grown, environment, fertility status of the soil, pest and disease

pressure and agronomic practices carried out for the crop.

5.6 Field efficacy of insecticides and biopesticides against major insect-pests of okra

The indiscriminate use of chemical pesticides in agriculture has led

to adverse effects, such as the development of pesticide resistance, pest

resurgence, emergence of new pests, pollution and health hazards. In view

of such adverse effects, present studies were carried out to evaluate the

effectiveness of some insecticides alone or in combination with the microbial

pesticides and a parasitoid, T. chilonis for the management of major insect-

pests infesting okra at two locations i.e. Palampur and Kachhiari during the

two seasons.

5.6.1 Cotton jassid, A. biguttula biguttula

The results showed that cypermethrin proved most superior in

reducing the population of jassids on okra followed by endosulfan at both

the locations during both the seasons (Table 4.32-4.35). Both these

insecticides have proved their worth in the past in checking jassid population

on okra (Babu and Azam, 1982; Mohan and Mohan, 1985, Yadav et al.,

1988; Dahiya et al., 1990; Singh et al., 1991; Adiroubane and

Letchoumanane, 1998; Patel and Patel, 1998; Singh and Chaudhary, 2001;

Singh, 2007; Sinha and Sharma, 2007).

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The treatments comprising azadirachtin and malathion showed

their effectiveness upto 9 days and were less effective than cypermethrin

and endosulfan. Dahiya et al. (1990) also reported the efficacy of malathion

against jassids on okra for a week whereas Jat (1981) observed malathion’s

effectiveness upto 12 days on okra. Malathion’s efficacy against okra jassids

has also been demonstrated by Singh (2007). Results in respect of lower

mortality of jassids afforded by malathion than synthetic pyrethroids in the

present study is in accordance with findings of Sucheta and Khokhar (1996).

Lower efficacy of neem based insecticide than synthetic

insecticides against A. biguttula biguttula in the present study is in

compliance with Thakur and Singh (1998) and Satpathy and Rai (1999).

However, Kumar and Singh (2001) and Mandal et al. (2006c) observed neem

based insecticides efficacious against jassid population on okra. This could

be because of the fact that the efficacy of an insecticide is related to the

number of its applications made, formulation and dosage used. The

moderate level of reduction because of azadirachtin in the current study

could be because of oviposition deterrent, repellent and growth inhibitory

action as has also been reported by Patel and Patel (1996) against okra

jassids.

Imidacloprid seed treatment and the combination treatment, B.

thuringiensis + endosulfan too showed consistently good performance in

suppressing A. biguttula biguttula population at different days after spray,

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however, the former was found effective only at Palampur. This could be

because of the reason that seed treatment with imidacloprid has been

known to be effective against early sucking pests, since jassid population

appeared later at Kachhiari (in relation to date of sowing of crop), therefore,

by that time, the efficacy of seed treatment might have been reduced.

A number of workers have reported the efficacy of imidacloprid

seed treatment against sucking pests for variable period i.e. upto 60 days

after germination by Mote et al. (1993) in cotton, upto 35 days after

germination by Sreelatha and Divakar (1997) in okra, upto 40 days after

germination by Patil et al. (1999) in cotton, , upto 50 days after germination

by Bhargava and Bhatnagar (2001) in okra whereas, Singh et al. (1996)

observed the effectiveness of the same insecticide in cotton upto 121 days.

The effectiveness of imidacloprid seed treatment against okra

jassids has been acknowledged in the past (Mote et al., 1993; Mote et al.,

1994; Sharma and Kalra, 1996; Sreelatha and Divakar, 1997; Patil et al.,

1999; Bhargava and Bhatnagar, 2001; Kumar and Singh, 2001; Kumar et al.,

2001; Lal et al., 2001; Anonymous, 2005a; Sinha and Sharma, 2007).

The synergistic effect of B. thuringiensis with sub-lethal doses of

safer insecticides has been earlier demonstrated against a number of pests

by a number of workers (Puri et al., 1988; Dabi et al., 1989; Butter et al.,

1995; Sharma and Odak, 1996; Tomar, 1998; Patel and Vyas, 1999; Sharma,

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2006). Mandal et al. (2006a) recorded minimum jassid population on okra in

B. thuringiensis + endosulfan treatment as compared to integration

treatment of B. thuringiensis with cartap, chlorpyriphos and amrutguard.

However, integration of imidacloprid with T. chilonis (both at half

dosages) did not prove effective. Mote et al. (1993) and Kumar and Singh

(2001) also observed that lower dose of imidacloprid (2.5 g kg -1 seed) was

not effective against A. biguttula biguttula. Moreover, T. chilonis is an egg

parasitoid of lepidopterous pests, therefore, it is quite obvious, that it must

have not parasitized eggs of jassids which is a homopteran pest. Also, T.

chilonis releases, B. thuringiensis, T. chilonis + B. thuringiensis and T.

chilonis + endosulfan were not found effective. The integrated treatment of

T. chilonis with B. thuringiensis and endosulfan did not show synergistic

effect since T. chilonis parasitizes eggs of only lepidopterous pests.

5.6.2 Cotton aphid, A. gossypii

In the present study, cypermethrin was the most effective

insecticide against okra aphids followed by endosulfan and B. thuringiensis +

endosulfan. Even azadirachtin and malathion were found effective but only

upto 9 days. Imidacloprid seed treatment also proved its efficacy but only at

Palampur (Tables 4.36-4.39). This is because of the early appearance of the

pest at Palampur (in relation to date of sowing of the crop) as compared to

Kachhiari, due to which the seed treatment might have been more

efficacious at the former location.

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The effectiveness of cypermethrin and endosulfan against A.

gossypii on okra has been acknowledged previously by many researchers in

their respective areas of study (Babu and Azam, 1982; Mohan and Mohan,

1985; Rai, 1985; Yadav et al., 1988; Rao et al., 1991; Bodhade et al., 1992;

Sosamma and Sheila, 1996; Patel et al., 1997b; Mishra, 2002; Sharma,

2004). Further, Ghosh et al. (1999) inferred high mortality of A. gossypii

(66.19%) on okra due to malathion.

Earlier also, imidacloprid seed treatment has been found effective

against okra aphids (Mote et al., 1993; Sreelatha and Divakar, 1997;

Anonymous, 2005a). A number of research workers (Dreyer and Hellpap,

1997; Chinniah and Ali, 2000; Mishra, 2002; Panickar et al., 2003; Mudathir

and Basedow, 2004) have reported the effectiveness of neem based

insecticides against A. gossypii on okra. In all these studies, 2 or more

applications of neem insecticides were made which resulted in good

suppression of aphid population. The lower efficacy of azadirachtin (upto

only 9 days) in the present investigation could be because of only single

spray made against this pest as against 2 or more sprays made by former

workers. Moreover, the effectiveness of a compound also varies with its

formulation, percentage of active ingredient, dosage, type of nozzle and

sprayer used.

The treatments which showed least worth against aphids in the

present study were T. chilonis, T. chilonis + imidacloprid, T. chilonis + B.

thuringiensis, B. thuringiensis and T. chilonis + endosulfan. Lower reduction

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evident in T. chilonis treatment either alone or in integration with B.

thuringiensis, endosulfan or imidacloprid was certainly because of the fact

that T. chilonis is an egg parasitoid of only lepidopterous pests, so obviously

it did not exhibit significant reduction either singly or in combination against

aphids. Also B. thuringiensis alone or in combination treatment did not prove

efficacious as B. thuringiensis has been known to infect mostly lepidopteran,

coleopteran and dipteran pests (Jaques, 1988; Biswas et al., 1996; Sharma

and Odak, 1996; Elanchezhyan et al., 2007) and A. gossypii, being a

homopteran pest experienced lower reduction in its population. Ghosh et al.

(1999) observed 35.35 per cent mortality of aphids on okra due to B.

thuringiensis.

5.6.3 Shoot and fruit borer, E. vittella

In the present study, cypermethrin and B. thuringiensis +

endosulfan showed least mean per cent fruit infestation by E. vittella at both

the locations during both the years (Table 4.40). The efficacy of

cypermethrin in checking population of shoot and fruit borer of okra is

corroborated by the findings of a number of earlier workers (Babu and

Azam, 1982; Krishnakumar and Srinivasan, 1984a; Krishnakumar and

Srinivasan, 1984b; Prasad et al., 1986; Gandhale et al., 1987; Singh and

Mishra, 1988; Peter and David, 1989; David and Kumaraswami, 1991; Shukla

et al., 1996; Rai and Satpathy, 1999; Ambekar et al., 2000b).

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The combination treatment of B. thuringiensis + endosulfan has

been found to be promising against E. vittella on okra by Tomar (1998) and

Mandal et al. (2006a). The present investigation also revealed the

effectiveness of endosulfan (although lower than cypermethrin) in lowering

the fruit infestation by shoot and fruit borer. This insecticide has been

reported effective against E. vittella in the past by many workers (Satpathy

and Mishra, 1970; Mote and Pokharkar, 1974; Uthamasamy and

Subramaniam, 1976; Verma et al., 1980; Sarkar and Nath, 1989;

Samuthiravelu and David, 1991; Pawar and Lawande, 1993; Gowri et al.,

2002; Manjanaik et al., 2002; Singh, 2007).

Other treatments which showed lower mean fruit infestation by E.

vittella were B. thuringiensis, T. chilonis + B. thuringiensis, azadirachtin and

malathion. The efficacy of B. thuringiensis and T. chilonis + B. thuringiensis

enhanced more by 15th day of spray, whereas that of azadirachtin and

malathion remained more effective for a week and their efficacy declined

thereafter. Taylor (1974), Krishnaiah et al. (1981), Mohan et al. (1983),

Singh et al. (1998), Tomar (1998), Ghosh et al. (1999), Patil et al. (2002)

and Gupta and Mishra (2006) have also observed the effectiveness of B.

thuringiensis against E. vittella on okra. The effectiveness of B. thuringiensis

upto 15 days after treatment against shoot and fruit borer on okra has been

formerly established by Satpathy and Panda (1997) thus, validating present

findings.

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The combination treatment of T. chilonis + B. thuringiensis was

found effective by Balakrishnan et al. (2004) in reducing the fruit damage by

another borer, H. armigera on cotton. The releases of T. chilonis against

shoot and fruit borer were not found much promising in the present study.

Similar observations regarding the lower efficacy of this parasitoid have been

made by Rao et al. (1978) and Sharma (2006). This could be ascribed to the

lower release rate (50,000 ha-1) of the parasitoid in the present study which

might have resulted in lower parasitism of eggs ultimately leading to

incomplete check in pest population. Sharma (2006) also mentioned similar

reasons for lower efficacy of T. chilonis against H. armigera on tomato.

Neem based insecticides have also shown their worth in checking

E. vittella incidence on okra formerly by Shukla et al. (1996) and Gajmer et

al. (2002). However, according to Sarode and Gabhane (1998), azadirachtin

was relatively ineffective in suppressing this pest. The difference in

efficiency of an insecticide could be ascribed to its formulation, percentage

of active ingredient, number of sprays and dosage used against the pest.

Malathion was reported effective earlier against E. vittella by Gupta and

Dhari (1978), Radke and Undirwade (1981), Verma (1985), Sarkar and Nath

(1989), Konar and Rai (1990), Shukla et al. (1996) and Singh (2007). The

comparatively higher performance of synthetic chemicals than neem based

insecticides against E. vittella as observed in the present study is in

accordance with the findings of Appaya (1990), Rao et al. (1991) and Shukla

et al. (1996).

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Imidacloprid seed treatment either alone or in integration with T.

chilonis at half dosages demonstrated poor performance against shoot and

fruit borers on okra. The present results find favour with Krishnaiah et al.

(1976) who noticed that okra seed treatment protected the crop from the

attack of E. vittella till the initiation of fruit set only which afterwards was

not found effective. Even Kumar et al. (1996) observed better reduction in E.

vittella infestation on okra by foliar applications rather than seed treatment.

5.6.4 Blister beetle, Mylabris spp.

In the current investigation, the synthetic pyrethroid, cypermethrin

undoubtedly proved to be the best in reducing Mylabris population on okra

followed by endosulfan. Even the integrated treatment of B. thuringiensis +

endosulfan performed consistently well against blister beetle. Moderate level

of protection (upto 9 days) was afforded by application of malathion and

azadirachtin. However, the remaining treatments viz. T. chilonis, B.

thuringiensis, imidacloprid, T. chilonis + imidacloprid, T. chilonis + B.

thuringiensis and T. chilonis + endosulfan illustrated lower efficacy against

this pest (Tables 4.41-4.44).

Literature pertaining to the effectiveness of synthetic chemicals

and biopesticides against blister beetle on okra is relatively scantly.

However, Kakar and Dogra (1988) and Kakar et al. (1990) validate the

present findings by reporting cypermethrin quite effective in reducing blister

beetle population in Himachal Pradesh on okra and French bean,

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respectively. Likewise, Chandel and Sood (1996) and Degri and Hadi (2000)

found cypermethrin highly efficacious against Mylabris beetles on cowpea

and rajmash, respectively. The efficacy of another synthetic pyrethroid viz.

lambda cyhalothrin has been illustrated by Sandal (2007) against M.

pustulata on pigeon-pea at Palampur (Himachal Pradesh).

Even the insecticide, endosulfan has been found to be promising in

suppressing blister beetle population previously by Kakar et al. (1990),

Chandel and Sood (1996) and Durairaj and Ganapathy (1999) on diverse

crops. The lower efficacy of malathion reported in the present study in

comparison to cypermethrin and endosulfan is corroborated by the findings

of Kakar et al. (1990), Chandel and Sood (1996), Degri and Chaudhary

(1998) and Degri and Hadi (2000).

5.6.5 Cotton leafroller, S. derogata

The present investigation revealed that the synthetic pyrethroid

cypermethrin proved best upto 9 days after spray, after which B.

thuringiensis + endosulfan was found more efficacious in reducing larval

population of S. derogata and remained effective even on 15 th day of spray.

In addition, other effective treatments were endosulfan, T. chilonis + B.

thuringiensis, B. thuringiensis, azadirachtin and malathion, the latter two

were effective upto 9 days of spray. On the other hand, the efficacy of T.

chilonis + B. thuringiensis, B. thuringiensis and B. thuringiensis + endosulfan

enhanced after 9 days of spray (Tables 4.45-4.48).

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The higher efficacy of cypermethrin than azadirachtin in checking

leafroller population on okra has been established earlier by Mishra et al.

(2002) in field trials conducted in Orissa. Sidhu and Dhawan (1979), Dhawan

et al. (1988) and Jafri et al. (1988) found endosulfan effective against

leafroller on cotton crop, thus supporting the current results.

The effectiveness of B. thuringiensis in suppressing S. derogata

population on okra has also been acknowledged earlier by Taylor (1974) and

Obeng and Sackey (2003). Neem based compounds have also proved their

capability in suppressing leafroller population in the past as reported by

Cobbinah and Owusu (1988), Anaso and Lale (2002) and Obeng and Sackey

(2003).

5.7 Effect of insecticides and biopesticides on marketable yield of okra All the insecticidal and biopesticidal treatments gave significantly

higher yield of okra over untreated check. The two year data at two

locations (Table 4.49) revealed that cypermethrin registered highest

marketable yield (100.29 to 127.40 q ha-1) whereas T. chilonis registered

lowest yield (48.76 to 66.62 q ha-1) of okra fruits. The other treatments

which recorded higher fruit yield were endosulfan, B. thuringiensis +

endosulfan, azadirachtin, imidacloprid and malathion (78.47 to 116.46 q

ha-1).

A number of research workers have reported higher yield of okra

fruits by the application of cypermethrin through reduction in the population

of various pests on this crop (Babu and Azam, 1982; Patel et al., 1984; Rai,

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1985; Gandhale et al., 1987; Narke and Suryawanshi, 1987; David and

Kumaraswami, 1991; Shukla et al., 1996; Singh and Chaudhary, 1999).

Likewise, worth of endosulfan in checking pest population on okra and giving

higher yields has been illustrated previously by Uthamasamy and

Subramaniam (1976); Jadhav and Nawale (1980); Verma et al. (1980);

Khaire and Naik (1986); Rao et al. (1991); Samuthiravelu and David (1991);

Singh et al. (1991); Patel et al. (1997b); Kumar and Singh (2001) and

Manjanaik et al. (2002).

The integrated treatment of B. thuringiensis + endosulfan was

reported effective in suppressing population of borers and jassids on okra

leading to higher fruit yield (Tomar, 1998; Mandal et al., 2006a). The higher

okra yield obtained from malathion treatment is in line with the findings of

Sarkar and Nath (1989), Konar and Rai (1990) and Borah (1995) because of

its efficacy in checking population of sucking, foliage and fruit pests. The

results pertaining to higher marketable yield obtained from endosulfan as

compared to neem based products is in consonance with research results of

Rao et al. (1991) and Patel et al. (1997b).

According to Mohan et al. (1983), Singh et al. (1998) and Gupta

and Mishra (2006), B. thuringiensis treatment checked borer incidence and

registered higher yield of okra, thus substantiating the current findings. Even

the imidacloprid seed treatment was found effective in enhancing okra yield

in the present study, by causing reduction in the population of sucking

pests. In the past also, comparable observations regarding efficacy of

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imidacloprid seed treatment have been made (Jotwani and Sarup, 1966;

Mote et al., 1993, Mote et al., 1994; Sreelatha and Divakar, 1997; Bhargava

and Bhatnagar, 2001; Dikshit et al., 2002; Anonymous, 2005a; Sinha and

Sharma, 2007).