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International Journal of Trend in Scientific Research and Development (IJTSRD)
Volume 4 Issue 4, June 2020 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470
@ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 776
Insecticidal Activity of Stem Bark Extract of Lophira Alata
(Ekki) Against Cowpea Bruchid (Callosobruchus Maculatus)
Ifelolu A. Remi-Esan1, Olusola O. Bankole2
1Environmental Biology Unit, 2Biochemistry Unit,
1,2Department of Science Laboratory Technology, Federal Polytechnic, Ilaro, Ogun State, Nigeria
ABSTRACT
Methanolic extract of Lophira alata was evaluated for its efficacy as contact
and fumigant insecticides on cowpea bruchid,Callosobruchusmaculatusinthe
laboratory at ambient tropical conditions of temperature and relative
humidity. The plant powder tested was applied at rates0.0(control),2.0gand
3.0 g / 20 g of cowpea seeds either directly for contact with the insect pest or
in plastic containers to assess its fumigant toxicity. Results of contact toxicity
assay showed that powders of L. alata was effective against the adult C.
maculatus causing 90 % mortality (4.00 ± 0.57) within 2 days ofapplicationat
3.0 g / 20 g of cowpea seeds as compared with 90 % mortality (5.38 ± 0.50)
recorded on day 4 of 2.0 g concentration application. The results of fumigant
assays showed that L. alata had the highest insecticidal activity causing 95 %
mortality of C. maculatus within 4 days of application at rate 3.0 g / 20g of
cowpea seeds in contrast to 80 % mortality recorded in 96 hrs of 2.0g
concentration application. The phytochemical screening of the plantrevealed
alkaloids, saponins, glycosides,phytosterols,tannis,flavonoidsandterpenoids
while reducing sugar was absent. This study showed that the tested plant
product is toxic to cowpea bruchid and the powders can be mixed with
cowpea seeds to prevent hatching of the eggs thereby helping in their
management.
KEYWORDS: Callosobruchus maculatus, Lophira alata, Fumigant, Cowpea,
Insecticidal
How to cite this paper: Ifelolu A. Remi-
Esan | Olusola O. Bankole "Insecticidal
Activity of Stem Bark Extract of Lophira
Alata (Ekki) Against Cowpea Bruchid
(Callosobruchus Maculatus)"Publishedin
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INTRODUCTION
Cowpea is one of the most significant pulse crops local to
Africa. Cowpea is called vegetable meat because of the high
measure of protein in grain with better organic incentive on
a dry weight premise. On a dry weight premise, cowpea
grain contains 23.4 percent protein, 1.8 percent fat,and60.3
percent sugars and it is rich in calcium and iron. Aside from
this, cowpea structures brilliant scrounge and it gives a
substantial vegetative development and spreads the ground
so well that it checkmates the soil erosion disintegration. As
a leguminous crop, it fixes around 70 – 240 kg for each ha of
nitrogen every year [1]. Cowpea is chiefly cultivated in
tropical and sub-tropical areas for its vegetable, seed and to
lesser degree as a fodder crop. It is an adaptablecropinview
of its covering nature, drought resistant nature, soil
reestablishing properties and multi-consumption methods.
As a pulse, cowpea fits well into a large portion of the
trimming frameworks of cropping [1]. The current day
cultivars display lower productivity, non-simultaneous
blooming and fruiting, non-reaction to high portions of
sources of organics like composts and fertilizers, water
system, culturing, resistance to major insect pest and
diseases which cause considerable damage and very poor
harvest [1]. The cowpea bruchid is planted and found
everywhere, with its underlying invasion beginning in the
field not long before harvest and are conveyed into the store
where it quickly increases [2,3]. Ripe and matured dry
cowpea seeds are used for preparing delicasies for
consumption purposes. In Nigeria, cowpea is associated to
pestivorus attack during pod and dry seed stages in the field
during cultivation and in storage after harvesting. C.
maculatus has caused huge weight reduction and reduced
market value of cowpea seeds [4]. It has been accounted for
that both quantitative and subjective loses emerging from
physical, chemical and biological factors happen during
stocking of grains in different forms of facilities and stores
[4].
The control of insect pests of stored grains and pulses are
achieved through useofsyntheticchemical insecticides,such
as methyl bromide. Several nations have however banned
the usage due to environmental concernsandhealthhazards
associated to human consumption of these grains [5]. The
adverse effects of chemical insecticides haveledresearchers
to try to find new avenue of insect control, which has led to
the discovery of plant products as an alternative way of
controlling insects [6,7]. Moreover, tropical regions are
believed to be endowed with many plant species with
insecticidal properties and some of them are with medicinal
properties [1]. Therefore, this research investigates the
insecticidal activity of oil extracts Ekki (Lophira alata)
against C. maculatus which is an important insect pests of
cowpea in storage.
IJTSRD31207
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@ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 777
Materials and methods
Study area
The study was conducted in the Zoology Departments
Research Laboratory, University ofLagosandPharmacology
Department Laboratory, Lagos UniversityTeachingHospital
Lagos.
Insect culture
The insects used to establish a laboratory colony of C.
maculatus came from a batch of infested cowpea seeds,
Vigna unguiculata (L.) Walp variety Ifebrowncollectedfrom
Nigeria Stored Products Research Institute Lagos, Nigeria.
Beetles were reared subsequently by replacement of
devoured and infested cowpea seeds with fresh un-infested
cowpea seeds in 2-L kilner jars covered with muslin cloth to
allow air circulation. Insect rearing and the experiments
were carried out at ambient temperature of 28 + 2 oC and 75
+ 5 % relative humidity.
Plant collection
The plant evaluated in this work was Lophira alata (Stem
bark). It was obtained in fresh form, free of insecticidesfrom
LUFASI Nature Park, Eti-Osa, Lagos State, Nigeria and
authenticated by the Botany Department, University of
Lagos, Lagos State. The plant materials were rinsed in clean
water to remove sand and other impurities, cut into smaller
pieces before air dried in a well-ventilated laboratory for
four weeks and ground into very fine powder using a
mechanical blender. The powder was packed in plastic
containers with tight lids and stored in a refrigerator at 4 oC
prior to use.
Collection of cowpea seeds
Cowpea seeds used for this study were obtained from a
newly stocked seeds free of insecticides at Nigeria Stored
Products Research Institute Lagos State, Nigeria. Firstly, the
seeds were cleaned and disinfested by keeping at -5 oC for 7
days to kill all hidden infestations. This is because all the life
stages, particularly the eggs are very sensitive to cold [8].
The disinfested cowpea seeds were then placed inside a
Gallenkamp oven (model 250) at 40 oC for 4 hours [9] and
later air dried in the laboratory to prevent mouldiness [10]
before they were stored in plastic containers with tight lids.
Extract preparation
Hydroalchoholic extracts of L. alata was carried out using
cold extraction method. 730 g of the powder was weighed
using an analytical balance(OHAUS,model number: PA124),
and soaked separately in an extraction bottle containing 5
liters of absolute methanol and water in the ratio 8:2. The
mixture was stirred occasionally with a glass rod and
extraction was terminated after 72 hrs. The resulting
mixture was filtered using a double layermuslinblanketand
the solvent was evaporated using a rotary evaporator
(EYELA, model number SB-1300) at 30 to 40 oC with rotary
speed of 3 to 6 rpm for 8 hrs. The resultant moisture solid
was transferred into a desiccator for 24hrs to remove any
residual moisture, until a dry weight was achieved.Thesolid
extract was ground into a fine powder using a mortar and
pestle and the powder was stored at 40C in the refrigerator
prior to further use. [11].
Phytochemical screening
Phytochemical analysis and screening was carried out using
simple chemical tests to detect the presence of secondary
plant constituents such as alkaloids, tannins, flavonoids,
saponins, triterpenes, sterols, phenols, glycoside, reducing
sugar and soluble carbohydrate in the sample was carried
out as described by the general method of [12].
Test of contact toxicity of plant extract on adult
mortality, oviposition and progeny development of
Callosobruchus maculatus
Plant extract of L. alata was admixed with cowpea seeds at
the rates of 2.0g / 10g of cowpea seeds in 250ml plastic
containers. Ten pairs of adult C. maculatus (2 to 3 days old)
sexed according to the methods described by [13] were
introduced into the treated. Untreated cowpea seeds were
similarly infested. Four replicates of the treated and
untreated controls were laid out in Complete Randomized
Block Design in insect cage. Insect mortality was assessed
every 24 hours for four days. Adults were assumed dead
when probed with sharp objects and noresponseismade.At
the end of day 4, all insects, both dead and alive were
removed from each container.
Test of plant extract as fumigant insecticide on adult
mortality, oviposition and progeny development of C.
maculatus
Ten grams of the cowpea seeds were weighed into 50ml
transparent plastic tubes that had been cut opened at the
bottom and sealed with muslin cloth. Plant extractofL. alata
weighing 2 and 3g concentrations were put into another
half-cut 25ml plastic tubes. The 50ml tube and 25ml tube
were then joined together with the aidofgum[14].Tenpairs
of adult C. maculatus (2 to 3 days old) sexed according to the
methods described above were introduced to the tube
containing 10g of cowpea seeds and tightly sealed [14].
Untreated cowpea seeds were similarly infested. Four
replicates of the treated and untreatedcontrolswerelaid out
in Complete Randomized Block Design in insect cage.
Bruchid mortality was assessedevery24hoursforfourdays.
Adults were assumed dead when probed with sharp objects
and made no responses. The experiment was kept insidethe
insect cage for another 30 days to allow fortheemergence of
the first filial (F1) generation. The number of adults that
emerged from each replicate was counted with an aspirator
and recorded. The percentage adult emergence was then
calculated using the method described by [13].
% Progeny development = No of adult emerged x 100
No of eggs laid 1
Statistical Analysis
Statistical Package for Social Science (SPSS, version 23) was
used in the analyses of the quantitative data. Data were
subjected to one-way analysis of variance (ANOVA). Where
significant differences existed, treatment means were
separated using the Tukey test and considered significant at
P ≤ 0.05.
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 778
Results
Phytochemical screening
The phytochemical analysis of the methanolic extract of Lophira alata stem bark reveals that the plant hasalkaloids,saponins,
glycosides, phytosterols, tannis, flavonoids and terpenoids while reducing sugar was absent as shown in Table 1 below.
Table 1: Result of phytochemical screening of the methanolic extract of Lophira alata stem bark
Phytoconstituents Lophira alata
Alkaloids +
Reducing sugar -
Saponins +
Glycosides +
Phytosterols +
Tannis +
Flavonoids +
Terpenoids +
Cyanide -
“+” represent class of phytochemicals present
“-” represent class of phytochemicals not present
Table 2: shows the percentage mortality, standard error of mean of adult Callosobrochus maculatus treated with
Lophira alata powder at rate 2.0 g / 20 g and 3.0 g / 20 g of cowpea seeds for contact toxicity.
Treatment
Mortality % ± SEM after
24hrs 48hrs 72hrs 96hrs
2g/20g 0.75 ± 0.25b 1.38 ± 0.18b 2.50 ± 0.19b 5.38 ± 0.50c
3g/20g 3.38 ± 0.46c 4.00 ± 0.57c 2.00 ± 0.68b 0.63 ± 0.38b
t-value
p-value
Control
5.01
0.02*
0.00 ± 0.00a
4.41
0.07*
0.00 ± 0.00a
0.71
0.02*
0.00 ± 0.00a
7.62
0.34*
0.00 ± 0.00a
Each value is a mean ± standard error of four replicates. Means within the same column, with different
letters are significantly different at P < 0.05 using Tukey’s test.
Effectiveness of plant powder as contact insecticide at rate 2.0 g / 20 g of cowpea seeds
Figure 1 presents the effect of plant powder on mortality of C. maculatus. Within 24 - 48 hrs of application. The plant powder
was less potent on the insects, causing 25 % mortality and at 72 hrs, about 35 % insect mortality was also recorded. The plant
powder had a significantly high mortality effect on the insects at 96 hrs (Day 4), killing 90 % of the tested insects.
Figure 1: Percentage mortality of adult C. maculatus treated with powder of L. alata at 2.0 g / 20 g cowpea
seeds for contact toxicity
Effectiveness of plant powder as contact insecticide at rate 3.0 g / 20 g of cowpea seeds
Figure 2 presents the effect of plant powder on mortality of C. maculatus. The plant powder had a significantly high mortality
effect on the tested stored product insects at 24 - 48 hrs (Days 1-2), killing 90 % of the insects. However, the insect biomass
reduced as shown in the graph (Figure 2).
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@ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 779
Figure 2: Percentage mortality of adult C. maculatus treated with powder of L. alata at 3.0 g / 20 g cowpea seeds
for contact toxicity
Fumigant effect of plant powder of Lophira alata on adult Callosobrochusmaculatus atrateof2.0g/20g and3.0g/20
g cowpea seeds
At day 4 after post treatment, L. alata was able to cause 80 % of mortality of adult C. maculatus applied at 2.0 g / 20 g, days1,2,
and 3 had less mortality ranging from 15 %, 20 %, and 25 % respectively. The toxicities of the plantpowdertocowpea bruchid
increased with an increase in concentration and period of exposure to the plant powder as shown in figure 3 below.
Bruchid mortality was rapid and highest at early expose rate of 3.0 g / 20 g on cowpea with about 95 % mortality recorded
between 48hrs exposure time. While the powder remains veryactiveandpotentdueto itsincreasedconcentration asshownin
figure 4. The insect biomass had reduced before the day 4 (96 hrs) limit.
Figure 3: Percentage mortality of adult C. maculatus treated with powder of L. alata at 2.0 g / 20 g cowpea
seeds as fumigant insecticides
Figure 4: Percentage mortality of adult C. maculatus treated with powder of L. alata at 3.0g / 20g cowpea seeds as
fumigant insecticides.
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@ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 780
Discussion
Botanically derived insecticides are good alternatives to
popularly used synthetic chemical insecticides as many of
them have often times yielded positive results when been
used against insect pests of stored products, belonging to,
but not limited to Coleoptera and Lepidoptera [15]. Theyare
known to be easily biodegradable and not toxic to none
target organisms which oftentimes are species of flora and
fauna. The discovery of organochlorine and
organophosphate chemical insecticidesinthelate1930s and
early 1940s, botanical insecticides have remained an
important weapon in the farmers armoryinmanaginginsect
pests of their farm produce and consumables [16]. Many
Nigerian plant species are medicinal and are proven to be
effective against a wide range of insect pests [17-19].
In this current study, the methanolic extract of Lophiraalata
stem bark show a high effectiveness, it caused 100%
mortality of C. maculatus within 48 hrs and 96 hrs of
application at all concentrations of 2.0g / 20g and 3.0g / 20g
of cowpea seeds. The powder may have also blocked the
spiracles of these insects which resulted in suffocation. This
results agree with the previous studies in which powders
and oils of A. indica, Z. zanthoxyloides, A. occidentale and M.
oleifera have been used as botanicals against different life
stages of storage insects [20, 1].
The preliminary phytochemical screening of methanolic
extract of Lophira alata stem barks revealed the presence of
alkaloids, tannins, saponins, phytosterols, flavonoids,
triterpenoids and glycosides. Alkaloids,flavonoids,saponins,
triterpenes and tannins have been reported to possess
central nervous system modifying activity such as
depression, sedation, anxiolysis, psychotropic,analgesicand
anti-convulsant activity [21-23]. The toxicity of L. alata to
the insect could be attributed to the presence of many
chemical ingredients such as triterpenoids, which includes
azadirachtin, salanin and meliantriol. [1]. The toxic effect of
L. alata could be related to the presence of secondary
phenolic compound known as phytosterols and this had
been reported to have mortality and ovicidal effectonstored
product insect pests [11, 19]. Also, thehighmortalityevoked
by the powder of L. alata, could be linked to the occurrence
of anacardic acid, cardinal, quercetin and kaempferol
glycosides as suggested by [24].
The inability of these insects to emerge may be due to the
death of the insect larvae which may occur due toinability of
the larvae to fully cast off their exoskeleton which remained
attached to the posterior part of their abdomen. This is in
agreement with the observation made by [25] who worked
on insecticidal propertiesofanalkaloidfromAlstoniaboonei.
Also, different chemical compositions of these plants as
mentioned earlier could be responsible for the in ability of
the adult insects to emerge as they are found to disrupt
growth and reduced larval survival as well as disruption of
life cycle of insects [26, 27].
This result agrees with the work of various researchers in
which the extracts and powders of A. indica, Z.
zanthoxyliodes, A. occidentale and M. oleifera were used to
prevent the emergence of adult insects as well as the
inhibition of their development [28, 11].
The high mortality and low progeny development caused by
the powder of L. alata can be attributed to strong choky
odour disrupting respiratory activity of the beetles. The
results obtained from this study agree with those reported
by [29] in studies with six Citrus species peel oils against C.
maculatus, S. zeamais and Dermestes maculatus.
In this study, the lethal effect of plant powder on the cowpea
bruchid could be as a result of contact toxicity. Insects
breathe by means of trachea which usually opens at the
surface of the body through spiracles [10]. These spiracles
might have been blocked by the powder thereby leading to
suffocation. The powder also prevented oviposition and
progeny development when applied as contact insecticides.
The choky effect of these powder also disrupt mating
activities, sexual communication and inhibit locomotion an
effect that have been reported by many researchers[30-32].
Conclusion
This research has proven that methanolic powder extract of
L. alata is a good and cheap means to control insect pests of
stored products, especially those insects in the order
Coleoptera which have characteristic biting and chewing
mouthparts and are clumsy fliers. Therefore, can be
integrated into other insect pest management systems for
effective pest control.
Acknowledgement
The authors are grateful to Dr F. Adetoro of Applied
Entomology and Pest Management Unit, Zoology
Department, University of Lagos for his timely intervention
in providing details on the identification and sexing of the
Bruchid used.
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[32] E. O. Maina, and N. E. S. Lale, “Efficacy of integrating
varietal resistance and neem (Azadirachtaindica)seed
oil for the management of Callosobruchus maculatus
infesting Bambara Groundnut in storage in storage”.
Nigerian Journal of Entomology, 2: 94 – 103.

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Insecticidal Activity of Stem Bark Extract of Lophira Alata Ekki Against Cowpea Bruchid Callosobruchus Maculatus

  • 1. International Journal of Trend in Scientific Research and Development (IJTSRD) Volume 4 Issue 4, June 2020 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470 @ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 776 Insecticidal Activity of Stem Bark Extract of Lophira Alata (Ekki) Against Cowpea Bruchid (Callosobruchus Maculatus) Ifelolu A. Remi-Esan1, Olusola O. Bankole2 1Environmental Biology Unit, 2Biochemistry Unit, 1,2Department of Science Laboratory Technology, Federal Polytechnic, Ilaro, Ogun State, Nigeria ABSTRACT Methanolic extract of Lophira alata was evaluated for its efficacy as contact and fumigant insecticides on cowpea bruchid,Callosobruchusmaculatusinthe laboratory at ambient tropical conditions of temperature and relative humidity. The plant powder tested was applied at rates0.0(control),2.0gand 3.0 g / 20 g of cowpea seeds either directly for contact with the insect pest or in plastic containers to assess its fumigant toxicity. Results of contact toxicity assay showed that powders of L. alata was effective against the adult C. maculatus causing 90 % mortality (4.00 ± 0.57) within 2 days ofapplicationat 3.0 g / 20 g of cowpea seeds as compared with 90 % mortality (5.38 ± 0.50) recorded on day 4 of 2.0 g concentration application. The results of fumigant assays showed that L. alata had the highest insecticidal activity causing 95 % mortality of C. maculatus within 4 days of application at rate 3.0 g / 20g of cowpea seeds in contrast to 80 % mortality recorded in 96 hrs of 2.0g concentration application. The phytochemical screening of the plantrevealed alkaloids, saponins, glycosides,phytosterols,tannis,flavonoidsandterpenoids while reducing sugar was absent. This study showed that the tested plant product is toxic to cowpea bruchid and the powders can be mixed with cowpea seeds to prevent hatching of the eggs thereby helping in their management. KEYWORDS: Callosobruchus maculatus, Lophira alata, Fumigant, Cowpea, Insecticidal How to cite this paper: Ifelolu A. Remi- Esan | Olusola O. Bankole "Insecticidal Activity of Stem Bark Extract of Lophira Alata (Ekki) Against Cowpea Bruchid (Callosobruchus Maculatus)"Publishedin International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456- 6470, Volume-4 | Issue-4, June 2020, pp.776-781, URL: www.ijtsrd.com/papers/ijtsrd31207.pdf Copyright © 2020 by author(s) and International Journal ofTrendinScientific Research and Development Journal. This is an Open Access article distributed under the terms of the Creative CommonsAttribution License (CC BY 4.0) (http://creativecommons.org/licenses/by /4.0) INTRODUCTION Cowpea is one of the most significant pulse crops local to Africa. Cowpea is called vegetable meat because of the high measure of protein in grain with better organic incentive on a dry weight premise. On a dry weight premise, cowpea grain contains 23.4 percent protein, 1.8 percent fat,and60.3 percent sugars and it is rich in calcium and iron. Aside from this, cowpea structures brilliant scrounge and it gives a substantial vegetative development and spreads the ground so well that it checkmates the soil erosion disintegration. As a leguminous crop, it fixes around 70 – 240 kg for each ha of nitrogen every year [1]. Cowpea is chiefly cultivated in tropical and sub-tropical areas for its vegetable, seed and to lesser degree as a fodder crop. It is an adaptablecropinview of its covering nature, drought resistant nature, soil reestablishing properties and multi-consumption methods. As a pulse, cowpea fits well into a large portion of the trimming frameworks of cropping [1]. The current day cultivars display lower productivity, non-simultaneous blooming and fruiting, non-reaction to high portions of sources of organics like composts and fertilizers, water system, culturing, resistance to major insect pest and diseases which cause considerable damage and very poor harvest [1]. The cowpea bruchid is planted and found everywhere, with its underlying invasion beginning in the field not long before harvest and are conveyed into the store where it quickly increases [2,3]. Ripe and matured dry cowpea seeds are used for preparing delicasies for consumption purposes. In Nigeria, cowpea is associated to pestivorus attack during pod and dry seed stages in the field during cultivation and in storage after harvesting. C. maculatus has caused huge weight reduction and reduced market value of cowpea seeds [4]. It has been accounted for that both quantitative and subjective loses emerging from physical, chemical and biological factors happen during stocking of grains in different forms of facilities and stores [4]. The control of insect pests of stored grains and pulses are achieved through useofsyntheticchemical insecticides,such as methyl bromide. Several nations have however banned the usage due to environmental concernsandhealthhazards associated to human consumption of these grains [5]. The adverse effects of chemical insecticides haveledresearchers to try to find new avenue of insect control, which has led to the discovery of plant products as an alternative way of controlling insects [6,7]. Moreover, tropical regions are believed to be endowed with many plant species with insecticidal properties and some of them are with medicinal properties [1]. Therefore, this research investigates the insecticidal activity of oil extracts Ekki (Lophira alata) against C. maculatus which is an important insect pests of cowpea in storage. IJTSRD31207
  • 2. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 777 Materials and methods Study area The study was conducted in the Zoology Departments Research Laboratory, University ofLagosandPharmacology Department Laboratory, Lagos UniversityTeachingHospital Lagos. Insect culture The insects used to establish a laboratory colony of C. maculatus came from a batch of infested cowpea seeds, Vigna unguiculata (L.) Walp variety Ifebrowncollectedfrom Nigeria Stored Products Research Institute Lagos, Nigeria. Beetles were reared subsequently by replacement of devoured and infested cowpea seeds with fresh un-infested cowpea seeds in 2-L kilner jars covered with muslin cloth to allow air circulation. Insect rearing and the experiments were carried out at ambient temperature of 28 + 2 oC and 75 + 5 % relative humidity. Plant collection The plant evaluated in this work was Lophira alata (Stem bark). It was obtained in fresh form, free of insecticidesfrom LUFASI Nature Park, Eti-Osa, Lagos State, Nigeria and authenticated by the Botany Department, University of Lagos, Lagos State. The plant materials were rinsed in clean water to remove sand and other impurities, cut into smaller pieces before air dried in a well-ventilated laboratory for four weeks and ground into very fine powder using a mechanical blender. The powder was packed in plastic containers with tight lids and stored in a refrigerator at 4 oC prior to use. Collection of cowpea seeds Cowpea seeds used for this study were obtained from a newly stocked seeds free of insecticides at Nigeria Stored Products Research Institute Lagos State, Nigeria. Firstly, the seeds were cleaned and disinfested by keeping at -5 oC for 7 days to kill all hidden infestations. This is because all the life stages, particularly the eggs are very sensitive to cold [8]. The disinfested cowpea seeds were then placed inside a Gallenkamp oven (model 250) at 40 oC for 4 hours [9] and later air dried in the laboratory to prevent mouldiness [10] before they were stored in plastic containers with tight lids. Extract preparation Hydroalchoholic extracts of L. alata was carried out using cold extraction method. 730 g of the powder was weighed using an analytical balance(OHAUS,model number: PA124), and soaked separately in an extraction bottle containing 5 liters of absolute methanol and water in the ratio 8:2. The mixture was stirred occasionally with a glass rod and extraction was terminated after 72 hrs. The resulting mixture was filtered using a double layermuslinblanketand the solvent was evaporated using a rotary evaporator (EYELA, model number SB-1300) at 30 to 40 oC with rotary speed of 3 to 6 rpm for 8 hrs. The resultant moisture solid was transferred into a desiccator for 24hrs to remove any residual moisture, until a dry weight was achieved.Thesolid extract was ground into a fine powder using a mortar and pestle and the powder was stored at 40C in the refrigerator prior to further use. [11]. Phytochemical screening Phytochemical analysis and screening was carried out using simple chemical tests to detect the presence of secondary plant constituents such as alkaloids, tannins, flavonoids, saponins, triterpenes, sterols, phenols, glycoside, reducing sugar and soluble carbohydrate in the sample was carried out as described by the general method of [12]. Test of contact toxicity of plant extract on adult mortality, oviposition and progeny development of Callosobruchus maculatus Plant extract of L. alata was admixed with cowpea seeds at the rates of 2.0g / 10g of cowpea seeds in 250ml plastic containers. Ten pairs of adult C. maculatus (2 to 3 days old) sexed according to the methods described by [13] were introduced into the treated. Untreated cowpea seeds were similarly infested. Four replicates of the treated and untreated controls were laid out in Complete Randomized Block Design in insect cage. Insect mortality was assessed every 24 hours for four days. Adults were assumed dead when probed with sharp objects and noresponseismade.At the end of day 4, all insects, both dead and alive were removed from each container. Test of plant extract as fumigant insecticide on adult mortality, oviposition and progeny development of C. maculatus Ten grams of the cowpea seeds were weighed into 50ml transparent plastic tubes that had been cut opened at the bottom and sealed with muslin cloth. Plant extractofL. alata weighing 2 and 3g concentrations were put into another half-cut 25ml plastic tubes. The 50ml tube and 25ml tube were then joined together with the aidofgum[14].Tenpairs of adult C. maculatus (2 to 3 days old) sexed according to the methods described above were introduced to the tube containing 10g of cowpea seeds and tightly sealed [14]. Untreated cowpea seeds were similarly infested. Four replicates of the treated and untreatedcontrolswerelaid out in Complete Randomized Block Design in insect cage. Bruchid mortality was assessedevery24hoursforfourdays. Adults were assumed dead when probed with sharp objects and made no responses. The experiment was kept insidethe insect cage for another 30 days to allow fortheemergence of the first filial (F1) generation. The number of adults that emerged from each replicate was counted with an aspirator and recorded. The percentage adult emergence was then calculated using the method described by [13]. % Progeny development = No of adult emerged x 100 No of eggs laid 1 Statistical Analysis Statistical Package for Social Science (SPSS, version 23) was used in the analyses of the quantitative data. Data were subjected to one-way analysis of variance (ANOVA). Where significant differences existed, treatment means were separated using the Tukey test and considered significant at P ≤ 0.05.
  • 3. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 778 Results Phytochemical screening The phytochemical analysis of the methanolic extract of Lophira alata stem bark reveals that the plant hasalkaloids,saponins, glycosides, phytosterols, tannis, flavonoids and terpenoids while reducing sugar was absent as shown in Table 1 below. Table 1: Result of phytochemical screening of the methanolic extract of Lophira alata stem bark Phytoconstituents Lophira alata Alkaloids + Reducing sugar - Saponins + Glycosides + Phytosterols + Tannis + Flavonoids + Terpenoids + Cyanide - “+” represent class of phytochemicals present “-” represent class of phytochemicals not present Table 2: shows the percentage mortality, standard error of mean of adult Callosobrochus maculatus treated with Lophira alata powder at rate 2.0 g / 20 g and 3.0 g / 20 g of cowpea seeds for contact toxicity. Treatment Mortality % ± SEM after 24hrs 48hrs 72hrs 96hrs 2g/20g 0.75 ± 0.25b 1.38 ± 0.18b 2.50 ± 0.19b 5.38 ± 0.50c 3g/20g 3.38 ± 0.46c 4.00 ± 0.57c 2.00 ± 0.68b 0.63 ± 0.38b t-value p-value Control 5.01 0.02* 0.00 ± 0.00a 4.41 0.07* 0.00 ± 0.00a 0.71 0.02* 0.00 ± 0.00a 7.62 0.34* 0.00 ± 0.00a Each value is a mean ± standard error of four replicates. Means within the same column, with different letters are significantly different at P < 0.05 using Tukey’s test. Effectiveness of plant powder as contact insecticide at rate 2.0 g / 20 g of cowpea seeds Figure 1 presents the effect of plant powder on mortality of C. maculatus. Within 24 - 48 hrs of application. The plant powder was less potent on the insects, causing 25 % mortality and at 72 hrs, about 35 % insect mortality was also recorded. The plant powder had a significantly high mortality effect on the insects at 96 hrs (Day 4), killing 90 % of the tested insects. Figure 1: Percentage mortality of adult C. maculatus treated with powder of L. alata at 2.0 g / 20 g cowpea seeds for contact toxicity Effectiveness of plant powder as contact insecticide at rate 3.0 g / 20 g of cowpea seeds Figure 2 presents the effect of plant powder on mortality of C. maculatus. The plant powder had a significantly high mortality effect on the tested stored product insects at 24 - 48 hrs (Days 1-2), killing 90 % of the insects. However, the insect biomass reduced as shown in the graph (Figure 2).
  • 4. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 779 Figure 2: Percentage mortality of adult C. maculatus treated with powder of L. alata at 3.0 g / 20 g cowpea seeds for contact toxicity Fumigant effect of plant powder of Lophira alata on adult Callosobrochusmaculatus atrateof2.0g/20g and3.0g/20 g cowpea seeds At day 4 after post treatment, L. alata was able to cause 80 % of mortality of adult C. maculatus applied at 2.0 g / 20 g, days1,2, and 3 had less mortality ranging from 15 %, 20 %, and 25 % respectively. The toxicities of the plantpowdertocowpea bruchid increased with an increase in concentration and period of exposure to the plant powder as shown in figure 3 below. Bruchid mortality was rapid and highest at early expose rate of 3.0 g / 20 g on cowpea with about 95 % mortality recorded between 48hrs exposure time. While the powder remains veryactiveandpotentdueto itsincreasedconcentration asshownin figure 4. The insect biomass had reduced before the day 4 (96 hrs) limit. Figure 3: Percentage mortality of adult C. maculatus treated with powder of L. alata at 2.0 g / 20 g cowpea seeds as fumigant insecticides Figure 4: Percentage mortality of adult C. maculatus treated with powder of L. alata at 3.0g / 20g cowpea seeds as fumigant insecticides.
  • 5. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD31207 | Volume – 4 | Issue – 4 | May-June 2020 Page 780 Discussion Botanically derived insecticides are good alternatives to popularly used synthetic chemical insecticides as many of them have often times yielded positive results when been used against insect pests of stored products, belonging to, but not limited to Coleoptera and Lepidoptera [15]. Theyare known to be easily biodegradable and not toxic to none target organisms which oftentimes are species of flora and fauna. The discovery of organochlorine and organophosphate chemical insecticidesinthelate1930s and early 1940s, botanical insecticides have remained an important weapon in the farmers armoryinmanaginginsect pests of their farm produce and consumables [16]. Many Nigerian plant species are medicinal and are proven to be effective against a wide range of insect pests [17-19]. In this current study, the methanolic extract of Lophiraalata stem bark show a high effectiveness, it caused 100% mortality of C. maculatus within 48 hrs and 96 hrs of application at all concentrations of 2.0g / 20g and 3.0g / 20g of cowpea seeds. The powder may have also blocked the spiracles of these insects which resulted in suffocation. This results agree with the previous studies in which powders and oils of A. indica, Z. zanthoxyloides, A. occidentale and M. oleifera have been used as botanicals against different life stages of storage insects [20, 1]. The preliminary phytochemical screening of methanolic extract of Lophira alata stem barks revealed the presence of alkaloids, tannins, saponins, phytosterols, flavonoids, triterpenoids and glycosides. Alkaloids,flavonoids,saponins, triterpenes and tannins have been reported to possess central nervous system modifying activity such as depression, sedation, anxiolysis, psychotropic,analgesicand anti-convulsant activity [21-23]. The toxicity of L. alata to the insect could be attributed to the presence of many chemical ingredients such as triterpenoids, which includes azadirachtin, salanin and meliantriol. [1]. The toxic effect of L. alata could be related to the presence of secondary phenolic compound known as phytosterols and this had been reported to have mortality and ovicidal effectonstored product insect pests [11, 19]. Also, thehighmortalityevoked by the powder of L. alata, could be linked to the occurrence of anacardic acid, cardinal, quercetin and kaempferol glycosides as suggested by [24]. The inability of these insects to emerge may be due to the death of the insect larvae which may occur due toinability of the larvae to fully cast off their exoskeleton which remained attached to the posterior part of their abdomen. This is in agreement with the observation made by [25] who worked on insecticidal propertiesofanalkaloidfromAlstoniaboonei. Also, different chemical compositions of these plants as mentioned earlier could be responsible for the in ability of the adult insects to emerge as they are found to disrupt growth and reduced larval survival as well as disruption of life cycle of insects [26, 27]. This result agrees with the work of various researchers in which the extracts and powders of A. indica, Z. zanthoxyliodes, A. occidentale and M. oleifera were used to prevent the emergence of adult insects as well as the inhibition of their development [28, 11]. The high mortality and low progeny development caused by the powder of L. alata can be attributed to strong choky odour disrupting respiratory activity of the beetles. The results obtained from this study agree with those reported by [29] in studies with six Citrus species peel oils against C. maculatus, S. zeamais and Dermestes maculatus. In this study, the lethal effect of plant powder on the cowpea bruchid could be as a result of contact toxicity. Insects breathe by means of trachea which usually opens at the surface of the body through spiracles [10]. These spiracles might have been blocked by the powder thereby leading to suffocation. The powder also prevented oviposition and progeny development when applied as contact insecticides. The choky effect of these powder also disrupt mating activities, sexual communication and inhibit locomotion an effect that have been reported by many researchers[30-32]. Conclusion This research has proven that methanolic powder extract of L. alata is a good and cheap means to control insect pests of stored products, especially those insects in the order Coleoptera which have characteristic biting and chewing mouthparts and are clumsy fliers. Therefore, can be integrated into other insect pest management systems for effective pest control. Acknowledgement The authors are grateful to Dr F. Adetoro of Applied Entomology and Pest Management Unit, Zoology Department, University of Lagos for his timely intervention in providing details on the identification and sexing of the Bruchid used. References [1] K. D. Ileke, and M. O. Oni, “Toxicity of some plant powders to maize weevil, Sitophilus zeamais on stored wheat grains”. African Journal of AgriculturalResearch. 6 (13): 3043 – 3048. [2] T. I. Ofuya, “Pest of stored cereals and pulses in Nigeria”. In: Ofuya TI and Lale NES (Eds.), Biology, Ecology and Control of Insect Pests of Stored Food Legumes. 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