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International Journal of Entomology and Nematology Research
Vol.1, No.1, pp.1-12, June 2016
___Published by European Centre for Research Training and Development UK (www.eajournals.org)
1
EFFECT OF DIFFERENT TEMPERATURES ON SOME BIOLOGICAL
PARAMETERS OF ANISOPTEROMALUS CALANDRAE, (HOWARD)
(HYMENOPTERA: PTEROMALIDAE) AND POPULATION FLUCTUATION OF
THE PARASITOID AND THEIR INSECT HOSTS OF THE GENUS SITOPHILUS
(COLEOPTERA: CURCULIONIDAE)
El-Aw M. A1*, S. I. S. Askar1, A. M. Abd El-Latif2, and M. S. Al-Assaal2
1Plant Protection Department, Faculty of Agriculture, Damanhour University, Egypt. 2Plant Protection Research Institute, Agriculture Research Center, Giza, Egypt.
ABSTRACT: Population fluctuation of some different insect species of the genus Sitophilus
(Coleoptera: Curculionidae) and their parasitoid, Anisopteromalus calandrae, (Howard)
(Hymenoptera: Pteromalidae) were studied at El-Beheira Governorate (Egypt). The present
results show that during the first year 2013 S. oryzae reached its peak in August where the
average number was 510 adult per kilogram wheat. While S. granarius and S. zeamais
reached its peak at December and September achieved 401 and 300 adults per kilogram
grain, respectively. The parasitoid A. calandrae was active from March to November and
reached its peak in August achieved 112 parasitoid per kilogram. The parasitoid sex ratios of
A. calandrae increased gradually with increasing temperature and reached its peak in
August of the year 2013 recorded 2.3 female to 1male. The duration of immature stages of
the parasitoid A. calandrae decreased with increasing temperature where it was extended
from 26.89 day at 20°C to 11.55 day at 35°C. The parasitoid total numbers also increased
gradually with increasing temperature from 20°C to 30 °C, recorded 67.67 at 30 °C. Then,
the numbers decreased also at 35 °C recorded 62.67. The results illustrated also that there
were significant difference in sex ratio between the temperature of 20 °C and 35 °C. Where,
at 20°C the sex ratio was 2 females:1male. Whilst, at 35 °C the sex ratio was 2.3
females:1male. No significant differences in the sex ratio were observed between the
temperature of 20, 25 °C and 30 °C. From the previous results the temperature of 30 °C was
the most desirable temperature for the activity of the parasitoid.
KEYWORDS: Temperature, Biological Parameter, Anisopteromalus Calandrae, Population,
Parasitoid, Insect Hosts
INTRODUCTION
Cereal grains are the major source of food for humans and most domesticated animals.
Insects are a major cause of post-harvest losses of stored foods and food products the world
over. Stored-product insect infestation can occur beginning at harvest and continuing through
bulk storage (Mansoor-ul-Hasan et al., 2006).
Weevils, Sitophilus granarius (L.), Sitophilus oryzae (L.) and Sitophilus zeamais (Motsch.),
are classified as the most important primary pests of stored wheat, whose adults damage
grains, and larvae inhabit and feed inside the grain (Rees, 2004; Beckett et al., 2007) and not
only reduce the grain quality but also produce a considerable amount of grain dust mixed
with frass.
International Journal of Entomology and Nematology Research
Vol.1, No.1, pp.1-12, June 2016
___Published by European Centre for Research Training and Development UK (www.eajournals.org)
2
One of the most promising alternatives to pesticides and fumigants for postharvest pest
management is biological control, which should be particularly effective in the closed
environment where grain is stored (Hansen and Steenberg., 2007).
Among natural enemies that could act as biological control agents of the wheat weevils, the
wasp Anisopteromalus calandrae (Howard) (Hymenoptera: Pteromalidae). It is a solitary
ectoparasitoid that parasitizes numerous stored-product beetles. Being a polyphagous
parasitoid, it can survive on a variety of internal feeding coleopteran hosts like S. zeamais
(Motschulsky) (Press et al., 1984; Williams and Floyd, 1971; Arbogast and Mullen., 1990),
S. oryzae (Lucas and Riudavets., 2002), S. granarius (Hansen and Steenberg., 2007),
Rhythopertha dominica (Coleoptera: Bostrichidae) (Ahmed., 1996 & Menon et al. 2002) and
Callosobruchus maculatus (Coleoptera: Bruchidae) (Ngamo et al., 2007). Biological control
of insects associated with stored products have been carried out of many authors worldwide.
In this region, the insects are recorded but their respective fluctuation of population of each
one during the year were not yet assessed.
The aim of the research reported herein was is first time to study and knowing the densities
of the insects (Sitophilus spp.) and their natural enemy A. calandrae associated with stored
grain cereals and in the second time to study the relationship between levels of the infestation
and the abundance of the parasitoid A. calandrae during the two years of study.
MATERIALS AND METHODS
Initial culture:
The rice weevil, Sitophilus oryzae (L.), and its parasitoid, A. calandrae, were obtained from
the Department of Plant Protection, Faculty of Agriculture, Damanhour University, Egypt.
For stock cultures of S. oryzae, many fixed numbers of rice weevils were continuously reared
on whole wheat grains free of insecticidal contamination for several generations in 1000 ml
glass gars. For stock cultures of A. calandrae, 100 adult females of A. calandrae were
introduced into a clear plastic box (15 cm width×30 cm length×6 cm height) containing 250
g of wheat infested with 4th instar rice weevils. All insects were reared at ambient conditions
(30±5 °C and 65±5% RH) and under natural photoperiod.
Population fluctuation of the insects of the genus Sitophilus and their parasitoid, A.
calandrae:
The experiment was carried out in Damanhour City to study the Population fluctuation of the
insects of the genus Sitophilus and their parasitoid, A. calandrae during two successive years,
2013 and 2014. Monthly averages of temperature (˚C) and relative humidity (%) were
obtained from the Central Laboratory for Agricultural Climate (CLAC), Egypt. The insects
are recorded but their respective population fluctuation of each one during the year was not
yet assessed in this region. Therefore, several insect samples were collected monthly for two
years. The experiment was conducted on a wide range of products such as wheat, maize and
rice from different localities and stored in varying quantities and different types of storage
facilities such as warehouse, silos, household and farm store. At the beginning of each
month, three samples each one about 1 kg in weight were collected randomly from several
locations. Samples were first analyzed in the laboratory by sieving the grain and examining
International Journal of Entomology and Nematology Research
Vol.1, No.1, pp.1-12, June 2016
___Published by European Centre for Research Training and Development UK (www.eajournals.org)
3
the insects using visual examinations and a binocular microscope. Samples were examined
twice during the month. Differences in numbers of the parasitoid and the weevils were
counted during the two years and the population fluctuation was recorded. The sex ratio of
the parasitoid was also determined from monthly field samples.
Effect of different temperatures on some biological parameters of the parasitoid A.
calandrae:
In the present study, the effect of different temperatures as abiotic factor on some biological
parameters such as the duration of immature stages, adult longevity, parasitoid total numbers
and the progeny sex ratio was examined. A huge numbers of unsexed adults from the
previous cultures of S. oryzae were added and allowed to mate and oviposit on 180 g of
whole wheat grain (Triticum aestivum L.) with about 14 % Moisture content (MC) in plastic
containers (19 cm width×19 cm length×8 cm height). Then, adult weevils were removed 7 d
later by passing the grains through a coarse sieve. After 25 days, four groups of temperature
were made (20, 25, 30 and 32 °C) by using the incubators (EHRET, Type BK 3108), each
with 70 % R.H and L12:D12 hours photoperiod. Each one consists of 3 replicates and
containing 15 g of infested wheat grain. A plastic cylindrical vials (250 ml) were used as
experimental units. According to Visarathanonth et al. (2010) ten 5-day adult females A.
calandrae uniform sizes from the rearing colony were used in this experiment where the
duration for egg laying is 11 d with the peak 12±5 insects on the 5th day and were introduced
for 24 h into each vial. Then, the females were removed. The vials of each group were
screened continuously and the timing of adult emergence (duration of immature stages), adult
longevity and the parasitoid total numbers were counted. The sex ratio of the parasitoid was
also examined.
Averages were calculated and compared by the One-way ANOVA. If ANOVA shows
significant inequality of the means, they were compared by Duncan multiple range test at 5%
probability level. The SPSS software (Version 10 for windows, SPSS Inc., Chicago, IL) was
used for statistical analysis.
RESULTS
Population fluctuation of the insects and their parasitoid A. calandrae during the first
year, 2013.
Data presented in Table (1) show that the three insect species of the genus Sitophilus were
found in all collected samples but their densities during the year of 2013 were different. The
obtained results clearly show that S. oryzae was the most widespread and destructive insect
pest of the genus Sitophilus in the tested region. On the other hand, S. zeamais was the least
widespread insect pest. The results also show that S. oryzae reached its peak in August where
the average numbers were 510 per kilogram. Whilst, S. granarius and S. zeamais reached its
peak at December and September achieved 401 and 300 per kilogram, respectively.
Regarding the parasitoid, A. calandrae was active from March to November and reached its
peak in August achieved 112 parasitoid per kilogram. The relationship between the
temperature and the parasitoid sex-ratio was positive. Where, the parasitoid sex ratios of A.
calandrae increased gradually with increasing temperature and reached its peak in August of
International Journal of Entomology and Nematology Research
Vol.1, No.1, pp.1-12, June 2016
___Published by European Centre for Research Training and Development UK (www.eajournals.org)
4
the year 2013 recorded 2.3 female to 1male. The sex ratio ranged between 2:2.3 female per 1
male.
Table 1: Population fluctuation of weevils and the parasitoid (year 1, 2013) at El-Behira
governorate:
Mon
th
Sitophilus spp. (Mean±SE) A. Calandrae
r R P/I S.
oryzae)
S.
granarius
(Mean±S
E)
S.
zeamais
(Mean±
SE)
average
(Mean±S
E)
Number
of female
progeny
(Mean ±
SE)
Number
of male
progeny
(Mean±S
E)
Sex
ratio
(Mean
±SE)
Total
wasps
±SE
Jan 149.00k
±0.006
241.00g±
0.003
30.00l±
0.030
140.00 c
±0.005
0.00d
±0.00
0.00d
±0.00
0.00d
±0.00
0.00d
±0.00
0.0
0
0.0
0
0.0
0
Feb 43.00l±0
.019
63.00l±0
.011
32.00k
±0.028
46.00 g
±0.003
0.00d
±0.00
0.00d
±0.00
0.00d
±0.00
0.00d
±0.00
0.0
0
0.0
0
0.0
0
Mar 199.00j±
0.004
89.00k±0
.008
41.00j±
0.022
109.67k
±0.008
38.00c±0
.13
18.33c
±0.12
2.07c
±0.03
56.33c
±0.13
0.8
6
0.7
5
0.3
8
Apr 211.00i±
0.004
121.00j±
0.006
82.00i±
0.011
138.00c
±0.0005
39.67c
±0.12
18.67c
±0.12
2.12bc
±0.03
58.33c
±0.12
0.8
5
0.7
6
0.3
7
May 219.00h
±0.004
140.00i±
0.005
102.00g
±0.009
153.67b
±0.0006
46.33c
±0.11
21.67c
±0.10
2.14bc
±0.03
68.00c
±0.11
0.8
7
0.7
4
0.3
9
Jun 320.00f±
0.003
200.00h±
0.003
111.00f
±0.008
210.33a
±0.008
58.67b
±0.08
27.00b
±0.08
2.17b
±0.02
85.67b
±0.08
0.8
6
0.7
4
0.3
2
Jul 490.00b
±0.002
300.00f±
0.002
151.00d
±0.006
313.67h
±0.02
64.33b
±0.08
29.67b
±0.08
2.17b
±0.02
94.00b
±0.08
0.8
5
0.7
3
0.3
2
Aug 510.00a
±0.002
311.00e±
0.002
205.00c
±0.004
342.00d
±0.01
78.33a
±0.06
34.00a
±0.07
2.30a
±0.02
112.33a
±0.06
0.8
7
0.7
5
0.3
3
Sep 481.00c
±0.002
340.00d±
0.002
300.00a
±0.003
373.67d
±0.02
59.67b
±0.08
28.33b
±0.08
2.11bc
±0.03
88.00b
±0.08
0.9
1
0.8
3
0.2
5
Oct 400.00d
±0.002
367.00c±
0.002
269.00b
±0.003
345.33d
±0.03
45.33c
±0.11
21.33c
±0.11
2.13bc
±0.03
66.67c
±0.11
0.9
0
0.8
4
0.1
9
Nov 360.00e
±0.002
390.00b±
0.002
141.00e
±0.006
297.00h
±0.007
40.00c
±0.12
19.33c
±0.12
2.06c
±0.03
59.33c
±0.12
0.9
2
0.8
5
0.1
7
Dec 299.00g
±0.003
401.00a±
0.002
99.00h
±0.009
266.33h
±0.008
0.00d
±0.00
0.00d
±0.00
0.00d
±0.00
0.00d
±0.00
0.0
0
0.0
0
0.0
0
aver
age 348.9±0
.009
252.11±
0.005
150.1±
0.002
254.967
±0.004
47.033±
0.001
21.833±
0.001
1.927
±0.00
1
68.866±
0.002
L.S.D
5% 0.82 0.65 0.88 8.38 3.84 0.09 12.14
Note: the symbol [r] refers to Correlation coefficient; [R] refer to Linear Regression and [P/I]
refer to Total number of the parasitoid / Total number of weevils
Values in the same column followed by the same letter did not differ significantly at the 5 %
level (P ≥ 0.05, Waller-Duncan K ratio t test; SAS institute.
International Journal of Entomology and Nematology Research
Vol.1, No.1, pp.1-12, June 2016
___Published by European Centre for Research Training and Development UK (www.eajournals.org)
5
Fig. 1. Monthly averages of temperature (˚C) and relative humidity (%) between
January 2013 and December 2013 at Damanhour City. (From "CLAC" Central
Laboratory for Agricultural Climate).
Population fluctuation of the insects and their parasitoid A. calandrae during the second
year, 2014:
The data represented in Table (2) showed that, the three insect species of the genus Sitophilus
were also found in all collected samples and their densities were also different during the
year, 2014. The obtained results are in harmony with that recorded at the previous year,
2013. Where S. oryzae was the most widespread and destructive insect pest of the genus
Sitophilus and S. zeamais was the least widespread insect pest in this region. Our data
showed that S. oryzae reached its peak in September where the average numbers were 486
insect per kilogram. On the other hand, S. granarius and S. zeamais reached its peak at
November and October achieved 421 and 333 insect per kilogram, respectively. Table (2)
also summarized that the parasitoid A. calandrae was active from march to November and
reached its peak in August achieved 121 parasitoid per kilogram. These results supported the
recorded data of the year 2013. In field collected samples as is clear from Table (2) and Fig
(2), there was a positive relationship between the temperature and the parasitoid sex-ratio.
Where, the parasitoid sex ratios of A. calandrae increased gradually with increasing
temperature and reached its peak in August of each year and recorded 2.3 female to 1male.
The sex ratio ranged between 2:2.3 female per 1 male.
Table (2): Population fluctuation of weevils and the parasitoid (year 2, 2014) at El-
Beheira governorate:
0
10
20
30
40
50
60
70
80
Jan-
13
Feb-
13
Mar
-13
Apr
-13
May
-13
Jun-
13
Jul-1
3
Aug
-13
Sep
-13
Oct-1
3
Nov
-13
Month
Temperature © Relative Humidity (%)
Month
Sitophil
us spp.
(Mean
±SE)
A. C
alandra
e
r R P/I
S.
oryzae
S.
granari
us
(Mean
±SE)
S.
zeama
is
(Mean
±SE)
Avera
ge
(Mean
± SE)
Number
of
female
progeny
(Mean±
SE)
Number
of male
progeny
(Mean±
SE)
Sex
ratio
(Mean
±SE)
wasps
(total
±SE)
Jan 200.00k
± 0.004
199.00h
± 0.012
56.00l
±
0.015
151.67k
±0.006
0.00f±
0.00
0.00e±
0.00
0.00d±0
.00
0.00f ±
0.00
0.
00
0.0
0
0.0
0
Feb 140.00l
± 0.006
80.00l±
0.030
77.00k
±
99.00d
±0.004
0.00f±
0.00
0.00e±
0.00
0.00d±
0.00
0.00f ±
0.00
0.
00
0.0
0
0.0
0
International Journal of Entomology and Nematology Research
Vol.1, No.1, pp.1-12, June 2016
___Published by European Centre for Research Training and Development UK (www.eajournals.org)
6
Note: the symbol [r] refers to Correlation coefficient; [R] refer to Linear Regression and [P/I]
refer to Total number of the parasitoid / Total number of weevils
Values in the same column followed by the same letter did not differ significantly at the 5 %
level (P ≥ 0.05, Waller-Duncan K ratio t test; SAS institute.
Fig. 2. Monthly averages of temperature (˚C) and relative humidity (%) between
January 2014 and December 2014 at Damanhour City. (From "CLAC")
0
10
20
30
40
50
60
70
80
Jan-
14
Feb-1
4
Mar
-14
Apr
-14
May
-14
Jun-
14
Jul-1
4
Aug
-14
Sep
-14
Oct-1
4
Nov-
14
Month
Temperature © 14.7 Relative Humidity (%) 79..3
0.011
Mar 206.00j
± 0.004
110.00k
± 0.022
89.00j
±
0.009
135.00d
±0.008
34.67e±
0.11
16.67d±
0.13
2.08bc±
0.04
51.33e±
0.11
0.
98
0.9
7
0.3
8
Apr 237.00i
± 0.004
133.00j
± 0.018
106.00i±
0.008
158.67k
±0.009
39.67de±
0.10
19.33d±
0.11
2.05c±
0.04
59.00de±
0 .10
0.
97
0.9
8
0.3
7
May 239.00h
± 0.004
138.00i
± 0.017
119.00h±
0.007
165.33k
±0.008
43.33d±
0.09
20.33d±
0.10
2.13bc±
0.04
63.67d±
0.09
0.
99
0.9
6
0.3
9
Jun 299.00g
± 0.003
221.00g
± 0.011
230.00e±
0.004
250.00f
±0.006
53.33c±
0.07
26.00c±
0.08
2.05c±
0.04
79.33c±
0.07
0.
99
0.9
9
0.3
2
Jul 395.00e
± 0.002
253.00e
± 0.010
252.00d±
0.003
300.00b
±0.009
66.00b±
0.06
30.00b±
0.07
2.21ab±
0.04
96.00b±
0.06
0.
97
0.9
8
0.3
2
Aug 479.00b
± 0.002
329.00d
± 0.007
289.00c±
0.003
365.67b ±0.02
85.00a±
0.05
36.67a±
0.06
2.33a±
0.04
121.67a±
0 .05
0.
98
0.9
7
0.3
3
Sep 486.00a
± 0.002
360.00c
± 0.007
300.00b±
0.003
382.00b ±0.04
64.67b±
0.06
30.00b±
0.07
2.16bc±
0.04
94.67b±
0.06
0.
45
0.2
0
0.2
5
Oct 470.00c
± 0.002
400.00b
± 0.006
333.00a±
0.003
401.00b ±0.07
50.33c±
0.08
24.33c±
0.09
2.08bc±
0.04
74.67c±
0.08
0.
46
0.1
9
0.1
9
Nov 461.00d
± 0.002
421.00a
± 0.006
200.00f±
0.004
360.67b ±0.06
40.67de±
0.09
19.67d±
0.11
2.07b±
0.04
60.33de±
0.09
0.
44
0.2
1
0.1
7
Dec 320.00f
± 0.003
239.00f
± 0.010
143.00g±
0.006
234.00f
±0.02
0.00f±
0.00
0.00e±
0.00
0.00d±
0.00
0.00f±
0.00
0.
00
0.0
0
0.0
0
average 345.88±
0.004
260.4±
0.002
206.1±
0.004
275.234
±0.005
47.767±
0.001
22.63±0.
001
1.916±
0.001
70.067±0
.01
L.S.D5
% 0.83 2.35 0.82 6.52 3.55 0.15 9.65
International Journal of Entomology and Nematology Research
Vol.1, No.1, pp.1-12, June 2016
___Published by European Centre for Research Training and Development UK (www.eajournals.org)
7
Effect of different temperatures on some biological parameters of the parasitoid
calandrae:
As shown in Table (3) the duration of immature stages of A. calandrae decreased with
increasing temperature where it was extended from 26.89 day at 20°C to 11.55 day at 35°C.
On the other hand, the parasitoid total numbers also increased gradually with increasing
temperature from 20°C to 30 °C, recorded 67.67 at 30 °C. Then, the numbers decreased also
at 35 °C recorded 62.67. Our results illustrated also that the temperature affect sex ratio. A
significant difference was observed in sex ratio between the temperature of 20 °C and 35 °C.
Where, at 20°C the sex ratio was 2 females:1male. Whilst, at 35 °C the sex ratio was 2.3
females:1male. There was no significant observed between the temperature of 20, 25 °C and
30 °C. From the previous results the temperature of 30 °C was the most desirable
temperature for the activity of the parasitoid.
Table (3): Effects of different temperatures on lifespan, adult longevity, parasitism
success and progeny sex ratio of the parasitoid A. calandrae, at constant relative
humidity (70% RH).
Temp.
(˚C) lifespan
Adult Longevity (d). Total
numbers
of
Emerged
parasitoids
Progeny
Sex
Ratio
50% honey-water starved
Female Male Female Male
20 26.89a
± 0.02 37.14a±2.12 27.67a±3.4 2.5a±0.2 1.9a±0.2 46.67a± 0.2
2.00a±
0.2
25 15.79b±
0.04 19.35b±3.3 15.12b±2.64 2.1b±0.2 1.6b±0.2 54.33b± 0.2
2.17a±
0.06
30 12.45c±
0.1 14.22c±2.44 11.29c±1.11 1.7c±0.2 1.3c±0.2 67.67c± 0.4
2.23ab±
0.12
35 11.55d±
0.2 10.45d±1.33 8.19d±1.22 1.4d±0.2 1.1d±0.2 62.67d± 0.2
2.30b±
0.2
LSD (0.05) 0.1 0.65 0.39 0.19 0.19 0.10 0.17
Correlation - 0.90 - 0.92 - 0.94 - 0.98 - 0.96 0.86 0.84
Means within each column followed by the same letter are not significantly different; LSD
test at 0.05.
DISCUSSION
Tables (1 and 2) showed that the weevils of the genus Sitophilus were found during the two
years on all collected samples. The results revealed that the most important insect species
infesting the stored crops at Damanhour City were Sitophilus oryzae (L.), Sitophilus
granarius (L.) and Sitophilus zeamais (Motsch.), respectively. In a Survey conducted by El-
Sayed et al. (2008) of stored grain insects infesting stored crops in the middle delta of Egypt.
They found that a relatively higher number of S. oryzae was observed during January and
February at Kafr EI-Sheikh, Dakahlia, Gharbeya and Menoufeya on wheat and maximum
number at Kafer EI-Sheikh and Dakahlia in November and December on maize. As shown
Sitophilus oryzae (L.) reached its peak in August 2013 and September 2014. Where, the
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temperature ranged between 25-28 ˚C while the relative humidity ranged between 65-73 %
RH. So, our data were close to the data published by Singh et al. (1974) who showed that the
optimal conditions for development of S. oryzae are 30 ˚C and 75% RH. Development stops
if the temperature falls below 17 ˚C (Anon. 2009). In the case of Sitophilus granarius (L.),
the infestation can begin at temperatures as low as 15 ˚C (Anon., 2008). Our obtained data
revealed that S. granarius reached its peak in December 2013 and November 2014. Where,
the temperature began to decrease and ranged between 15-20 ˚C while the relative humidity
began to increase and ranged between 65-75 % RH. On the other hand Sitophilus zeamais
(Motsch.) reached its peak in October 2013 and October 2014. Where, the temperature
ranged between 22-24 ˚C and the relative humidity ranged between 63-67 % RH. (Throne
1994) revealed that the lower limit for development from egg to adult weevils of S. zeamais
was 15.6 ˚C and the upper limit was 32.5 ˚C at 75% RH.
Regarding the pteromalid parasitoid, our results indicated that the parasitoid Anisopteromalus
calandrae was also found during the two years except the three months of December,
January and February of each year. A nearly study conducted by (Ahmed, 1996) and revealed
that the parasitoid, A. calandrae was active in the field from February to November, but
reached its peak in July in Saudi Arabia. Disappearance of the parasitoid in December,
November and February may indicate that it avoids adverse conditions by passing these
months as a diapausing egg similar to bethylid species (Ahmed, 1989). Our results as
mentioned before revealed that, the parasitoid was active from Mars to November and
reached its peak in August of each year under Egyptian conditions. Differences in the peak of
the parasitoid between Egypt and Saudi Arabia due to hot conditions in July in Saudi Arabia
compared with Egypt conditions. In addition to that, numbers of the parasitoid increased with
increasing numbers of coleopteran species and with increasing temperature. So, our results
in agreement with that recorded by Menon et al., 2002 who found that the instantaneous
search rate of the parasitoid A. calandrae increased as temperature increased and increasing
with host density. Data summarize that, the parasitoid has the ability to synchronize its life
cycle to each of these hosts and that it becomes abundant during their availability. It seems
that a positive correlation existed between activity and atmospheric conditions which in turn
were related to abundance of the host (Rostom et al., 1990). As demonstrated in field
collected samples, the sex ratio of A. calandrae was affected by temperature. Where, the sex
ratio increased gradually with increasing temperature and reached its peak in August of each
year recorded 2.3 female to 1male. These results differ from those of Ghani and Sweetman
(1955), who mentioned that temperature and moisture did not seem to have any effect on the
proportion of sexes. Our obtained data also showed that the sex ratio of the parasitoid ranged
between 2-2.3 females per 1 male. Thereby, our data were close to those recorded by Ahmed
(1996) who found that, in field collected samples of parasitized host stages the sex ratio of A.
calandrae was 2.1 females to 1 male.
From data in Table (3) it could be easily noticed that, the variations in temperature at 70%
R.H. shorted both the durations of immature stages and adult longevity. The duration of
immature stages of A. calandrae decreased with increasing temperature where it was ranged
from 26.89 days at 20 ˚C to 11.55 days at 35˚C. Generally, at all temperatures, fed/starved
adult longevity of males was less than that of females. For example, at 20 °C, Adults fed
honey living up to 39.26 and 31.07 days for females and males, respectively. On the other
hand, starved adults living up to 2.7 and 2.1 days for females and males. As shown also,
Total numbers of Emerged parasitoids increased gradually with increasing temperature.
Where, the progeny production of A. calandrae was extremely low at lower temperature than
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9
at higher one and peak progeny production was achieved in optimum temperature of 30 °C
recorded 67.67 number/vial. Data illustrated also that the temperature affect sex ratio. At
35°C the sex ratio was 2.3 females: 1male. Non-significant difference was observed in sex
ratio between the temperatures of 20, 25 and 30 °C. It ranged between 2-2.23 females to 1
male. In addition to that no significant differences were observed also between the two
temperatures of 30 and 35 °C. From the previous results the temperature of 30 °C was the
most desirable temperature for the activity of the parasitoid A. calandrae.
Studies on the effects of constant temperatures on the development of different
hymenopteran parasites were carried out by several workers (Wallace and Sullivan 1963,
Sullivan 1965, Pilon et al. 1964, Heron 1967, and Philogene and Benjamin 1971). There is an
optimum temperature range for every insect species outside of which survival is severely
reduced (Jackson, 1966; Krishnamoorthy, 1989). The use of variable temperatures has
resulted in contradictory results. It is evident from data presented in Table ( 3 ) that the
duration of immature stages of A. calandrae decreased with increase of temperature. Where,
it was lasted 26.89, 15.79, 12.45 and 11.55 days at 20, 25, 30 and 35 ˚C at 70% RH,
respectively. These results comply with the view of (Ghani and Sweetman 1955). An
experiment on the biology of this parasitoid wasp was conducted by Visarathanonth et al.
(2010) who mentioned that for the wasp progenies in the Sitophilus zeamais when fed with
milled rice at 32.5 ˚C and 70% RH. The life span from eggs to adults was 11.4 day. Ahmed
(1996) reported that the duration of immature stages from egg to adult of A. calandrae when
reared on larvae of R. dominica lasted 18.9±2 (16-20) and 14.6±1.83 (12-15) days at the
temperatures of 26±2 and 30±2 ˚C, respectively at 60±5% RH. Similarly, adult A. calandrae
required 14 days to emerge from parasitized S. granarius (Sweetman, 1964). Okamoto
(1971) reported an 8- day delay of emergence of adult A. calandrae when younger larvae of
C. chinensis were used. According to Ahmed et al. (2013) the duration of immature stages
lasted (20.9-28.4), (10.9-16.2), (7.7-9.7) and (7.5-10.5) days for males and females at 20, 25,
30 and 35 ˚C, respectively at 70% RH.
Regarding adult longevity, it is an important factor in the population dynamics of parasitoids
and influences their effectiveness in exploiting host populations Eliopoulos et al. (2005).
Longevity is a variable specific characteristic, which is influenced by a range of biotic (host,
body size, mating, adult feeding, etc.) and abiotic (temperature, humidity, photoperiod)
factors (Jervis& Copland, 1996). Longevity of most insect species decreases with increasing
temperature within the optimum range. Our obtained data revealed that adult longevity of
both males and females of A. calandrae decreased with increasing temperature. In addition to
that fed/starved adult longevity of males was less than that of females at all tested
temperature. These obtained results supported the view of Ahmed (1996), who found that
mated female A. calandrae fed on honey, lived significantly longer 32.6±6.2 (32-37) days at
26±2 ˚C than at 30 ˚C 25.7±3.1 (21-30) days. The respective figures for males were 25.5±2.3
(22-30) and 11.7±1.9 (9-12) days at the same temperatures. Bare (1942), revealed that A.
calandrae females lived for 39 days and males for 22 days at room temperature (26 °C).
Ghani and Sweetman (1955) found higher longevity in A. calandrae when the female
received nutrition. Ahmed et al. (2013) mentioned that the adult males and females fed with
50% honey-water showed an increased longevity, compared to those receiving no food or
water. He also noted that a mated female lived a maximum period of 41 days, whereas a
starved female had a maximum life span of 12 days.
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Regarding total numbers of emerged parasitoids, numbers increased gradually with
increasing temperature and the optimum temperature was at 30 ˚C. these results in harmony
with that recorded by Ahmed et al. (2013), who obvious that the progeny production of A.
calandrae was extremely low at lower temperature than at higher ones and peak progeny
production was achieved in optimum temperature of 30 ˚C and 70% RH.
Regarding the effect of temperature on sex ratio, our data showed that the sex ratio was
affected significantly by temperature. It was ranged from 2-2.3 females to 1 male. a nearly
study conducted by Ahmed (1996) revealed that sex ratio was 2.3 females to 1 male in the
laboratory and 2.1 females to 1 male in the field. Ahmed et al. (2013) reported that at 20 ˚C
with higher relative humidity of 90% larger numbers of A. calandrae females were recorded
resulting in 75.2% females and the female : male sex ratio being 3.04 : 1. These results differ
from those of Ghani and Sweetman (1955), who mentioned that temperature and moisture
did not seem to have any effect on the proportion of sexes.
REFERENCES
Ahmed, K. N.; M. R. Hasan; H. Ahmed; M. A. Hannan and S. K. Ghose, 2013. Effects of
temperature, relative humidity and host on the biology of anisopteromalus calandrae
(hymenoptera: pteromalidae). Bangladesh J. Zool. 41(1): 87-96.
Ahmed, K. S. 1989. Biological and morphological aspects of the parasitoid Scleroderma
ephippium (Saunders) (Hymenoptera; Bethylidae). Bulletin de Sociefe entomologie
d’Egypte 68, 307-320.
Ahmed, K. S. 1996. Studies on the ectoparasitoid, Anisopteromalus calandrae How.
(Hymenoptera: Pteromalidae) as a biological control agent against the lesser grain
borer, Rhyzopertha dominica (Fab.) in Saudi Arabia. J Stored Prod Res 32 (2), 137–40.
Anonymous. 2008. Granary weevil, Sitophilus granarius (L.) Canadian Grain Commission.
Anonymous. 2009. Rice weevil, Sitophilus oryzae (L.) Canadian Grain Commission.
Arbogast, R. T. and M. A. Mullen. 1990. Interaction of maize weevil (Coleoptera:
Curculionidae) and parasitoid Anisopteromalus calandrae (Hymenoptera:
Pteromalidae) in a small bulk of stored corn. J Econ Entomol. 83 (6), 2462-8.
Bare, C. O., 1942. Some natural enemies of stored tobacco insects with biological notes.
Journal of Economic Entomology 35: 185-189.
Beckett, S. J., P. G. Fields, and B. Subramanyam. 2007. Disinfestation of stored products and
associated structures using heat. In: Heat Treatments for Postharvest Pest Control (Tang
J., Mitcham E., Wang S. and Lurie S., eds.), CAB International, UK, pp. 182-237.
Eliopoulos, P. A., G. J. Stathas and S. L. Bouras. 2005. Effects and interactions of
temperature, host deprivation and adult feeding on the longevity of the parasitoid
Venturia canescens (Hymenoptera: Ichneumonidae). Eur. J. Entomol. 102 (2): 181–
187.
El-Sayed, F. M. A.; A. E. Abdel Aziz; and S. A. Shemais. 2008. Survey of stored grain
insects infesting stored crops in the middle delta of Egypt. Bull. Ent. Soc. Egypt 85, 49-
59.
Floyd, E. H. and D. L. Newson. 1959. Biological study of the rice weevil complex. Annals of
the Entomological Society of America, 52, 687–695.
Ghani, M. A.; and H. L. Sweetman. 1955. Ecological studies on the granary weevil parasite,
Aplastomorpha calandrae (Howard). Biologia (Pakistan). 1, 115-139.
International Journal of Entomology and Nematology Research
Vol.1, No.1, pp.1-12, June 2016
___Published by European Centre for Research Training and Development UK (www.eajournals.org)
11
Halstead, D. G. H. 1963. External sex differences in storedproducts Coleoptera. Bull.
Entomol. Res. 54(1) : 118–134.
Hansen, L. S. and T. Steenberg. 2007. Combining larval parasitoids and an
entomopathogenic fungus for biological control of Sitophilus granarius (Coleoptera:
Curculionidae) in stored grain. Biol Cont. 40(4) : 237–42.
Heron, R. J. 1967. Heat tolerance of last-instar larvae of the larch sawfly, Pristiphora
erichsonii (Hymenoptera: Tenthredinidae). Can. Entomol. 99 :1150-1156.
Hidayat, P., T. W. Phillips and R. H. Ffrench-Constant. 1996. Molecular and morphological
characters discriminate Sitophilus oryzae and S. zeamais (Coleoptera: Curculionidae)
and confirm reproductive isolation. Annals of the Entomol. Society of America, 89,
645–652.
Jackson D, J. 1966. Observations on the biology of Caraphractus cinctus Walker
(Hymenoptera: Mymaridae), a parasitoid of the eggs of Dytiscidae (Coleoptera). III.
The adult life and sex ratio. Trans. R. Entomol. Soc. Lond. 118 : 23–49.
Jervis, M. A. & Copland M. J. W., 1996: The life cycle. In Jervis M. A. & Kidd N. (eds):
Insect Natural Enemies – Practical Approaches to their Study and Evaluation. Chapman
and Hall, London, pp. 63-161.
Jervis, M. A. and M. J. W. Copland. 1996. The life cycle. In Jervis M.A. & Kidd N. (eds):
Insect Natural Enemies – Practical Approaches to their Study and Evaluation. Chapman
and Hall, London, pp. 63–161.
Krishnamoorthy, A. 1989. Effect of cold storage on the emergence and survival of the adult
exotic parasitoid, Leptomastix dactylopii How. (Hym., Encyrtidae). Entomon. 14: 313–
318.
Kuschel, G. 1961. On problems of synonymy in the Sitophilus oryzae complex. Annals and
Magazine of Natural History Series, 13 :241–244.
Lucas E., J. Riudavets. 2002. Biological and mechanical control of Sitophilus oryzae
(Coleoptera: Curculionidae) in rice. J. Stored Prod Res. 38 (3): 293–304.
Mansoor-ul-Hasan, M. Sagheer, Aman Ullah, W. Wakil and A. Javed, 2006. Response of
Trogoderma granarium (Everts) to different doses of Haloxylon recurvum extract and
deltamethrin. Pak. Entomol. 28 ( 2):25 -30.
Menon, A., P. W. Flinn, A. Barry and B. A. Dover. 2002. Influence of temperature on the
functional response of Anisopteromalus calandrae (Hymenoptera: Pteromalidae), a
parasitoid of Rhyzopertha dominica (Coleoptera: Bostrichidae). J. Stored Product
Research 38 (5), 463–469.
Ngamo T. S. L., H. Kouninki, Y. D Ladang, M. B. Ngassoum, P. M. Mapongmestsem and T.
Hance. 2007. Potential of Anisopteromalus calandrae (Hymenoptera: Pteromalidae) as
biological control agent of Callosobruchus maculatus (F.) (Coleoptera: Bruchidae). Afr
J Agr Res 2 (4), 168–72.
Okamoto, K., 1971. The synchronization of the life cycles between Callosobruchus chinensis
(L.) and the parasite Anisopteromalus calandrae Howard. Japanese Journal of Ecology
21: 233-237.
Peng, W. K., H. C. Lin, , C. N. Chen and C. H. Wang. 2003. DNA identification of two
laboratory colonies of the weevils, Sitophilus oryzae (L.) and S. zeamais Motschulsky
(Coleoptera: Curculionidae) in Taiwan. J. Stored Products Research, 39 (2), 225–235.
Philogene, B. J. R. and D. M. Benjamin. 1971. Temperature photoperiod effects on the
immature stages and adults of Neodiprion swainei (Hym: Diprionidae). Can. Ent. 103:
1705-1715.
International Journal of Entomology and Nematology Research
Vol.1, No.1, pp.1-12, June 2016
___Published by European Centre for Research Training and Development UK (www.eajournals.org)
12
Pilon, J. G., H. A. Tripp, J. M. Mcleod and S. L. Ilnitzky.1964. Influence of temperature on
prespinning eonymphs of the swaine jackpine sawfly, Neodiprion swainei
(Hymenoptera: Diprionidae). Can. Ent. 96: 1450-1457.
Press, J. W., L. D. Cline and B.R. Flaherty. 1984. Suppression of residual populations of the
rice weevil, Sitophilus oryzae, by the parasitic wasp, Anisopteromalus calandrae. J. of
the Georgia Entomol. Society 19, 110–113.
Rees, D.P. 2004. (ed.): Insects of Stored Products. Manson Publishing, Ltd., UK.
Rostom, Z. F., S. A. Osman, A. E. Mussa, A. H. Abo-Hadeed and K. Abd-Elsalam. 1990.
Stored grain insects and fungi and their effects on grain and animal feed deterioration.
A project report for King Abd-El-Aziz City for Science and Technology, King Faisal
University, Saudi Arabia.
Singh, K., N. S. Agrawal and G. K. Girish.1974. The oviposition and development of
Sitophilus oryzae (L.) in different high-yielding varieties of wheat. J. Stored Products
Research, 10 (2): 105-111.
Sullivan, C. R. 1965. Laboratory and field investigations on the ability of eggs of the
European pine sawfly Neodiprion sertifer (Geoffroy) to with stand low winter
temperatures. Can. Ent. 97: 978-993.
Sweetman, H. L., 1964. The Principles of Biological Control. Brown Comp. Iowa, USA.
Throne, J. E. 1994. Life history of immature maize weevils (Coleoptera:Curculionidae) on
corn stored at constant temperatures and relative humidities in the laboratory. Environ.
Entomol. 23 (6): 1459-1471.
Visarathanonth, P., R. Kengkanpanich, J. Uraichuen, and J. Thongpan. 2010. Suppression of
Sitophilus zeamais Motschulsky by the ectoparasitoid, Anisopteromalus calandrae
(Howard). 10th International Working Conference on Stored Product Protection.755-
759.
Wallce, D. R. and C. R. Sullivan. 1963. Laboratory and field investigations of temperature on
the development of Neodiprion sertifer (Geoff.) in the cocoon. Can. Ent. 95: 1051-
1066.
Williams, R. N., E. H. Floyd. 1971. Effect of two parasitoids, Anisopteromalus calandrae
and Chaetospila elegans upon populations of the maize weevil under laboratory and
natural conditions. J. Econ. Entomol. 64: 1407-1408.