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Biological Forum – An International Journal 6(2): 90-93(2014) 
ISSN No. (Print): 0975-1130 
ISSN No. (Online): 2249-3239 
Biology of Hypsopygia postflava (Lepidoptera: Pyralidae), a Snout 
Moth Parasitic on the Nest of the Paper wasp Polistes olivaceus 
(Vespidae: Polistes) 
Phong Huy Pham 
Institute of Ecology and Biological Resources, 
Vietnam Academy of Science and Technology, 
18 Hoang Quoc Viet Road, Hanoi, Vietnam. 
(Corresponding author: Phong Huy Pham) 
(Received 08 July, 2014, Accepted 08 September, 2014) 
ABSTRACT: Hypsopygia postflava, a snout moth parasitic on the nest of the paper wasp Polistes 
olivaceus was reported first time, with studies on its biology. Head width of moth larvae from third 
instar and over was difficult to specify because of great variety. The duration of life cycle of H. postflava 
was 40.46±4.96 days, ranging from 33 to 49 days. Life time of both female adult and male adult was 
equal (in the 6-9 day range). Survivorship ratio was, for larvae 88%, and for pupae 82.5%. Sex ratio of 
H. postflava in laboratory experiments (♀:♂) was 1: 1.26 in comparison with 1: 1.55 of that of adult 
moths emerged from the nest of the paper wasp P. olivaceus. The average number of eggs having in the 
body of the female adult was 88.93. However female adults only laid a mean of 39.39 eggs during their 
lifetime. Female adults laid eggs singly or in clumps of a few eggs. The mean ratio of hatched eggs was 
very low (18.98%). 
Key words: Hypsopygia, Lepidoptera, lifetime, paper wasp, Pyralidae, snout moth 
INTRODUCTION 
Accidentally, on March 22, 2014 when I was 
concentrating on my study on the hibernation of the 
paper wasp, Polistes olivaceus (Pham, 2014), with 
field trips in Hanoi, I collected a nest of this wasp 
that it had strangeness in comparison with any nest 
which had been collected before. I decided to 
scrutinize the nest. 
On April 12, some adult moths emerged. It made me 
though whether this was one of moths parasitic on 
the nest of the paper wasp. I had decided to send 
specimens of the moth to a colleague of mine in 
Russian and then he informed me that this was a 
snout moth parasitic on the nest of the paper wasps, 
with its scientific name Hypsopygia postflava 
(Hampson, 1893). 
H. postflava is one of the snout moths belonging to the 
family Pyralidae, the order Lepidoptera. To date, in the 
world, studies on biology, habit or bionomics of the 
species have been only produced in Japan by Nakatani 
et al., (1999) with its parasite on the nest of Polistes 
jadwigae, and by Kato et al., (2007a,b) with its parasite 
on the nest of Polistes jokahamae. Those studies are 
about the life cycle, hibernation, mating, oviposition, 
and prey use by larvae of the species. Thus H. postflava 
is yet poorly studied. 
In Vietnam, to now, studies on taxonomy, biology, 
or bionomic of H. postflava belonging to family 
Pyralidae are yet very poor and still very lack of 
documents. However, so far I have not yet had a 
sufficiency of documents to certify that the snout 
moth H. postflava is a new record for Vietnam. With 
discovery of the pupae, and of emergence of adults 
on the nest of the paper wasp P. olivaceus, the 
present paper is to record its first parasite on the nest 
of the paper wasp P. olivaceus, with studies on its 
biology. 
MATERIALS AND METHODS 
A nest of the paper wasp P. olivaceus collected at 
Nghia Do precinct, Cau Giay district, Hanoi, Vietnam 
(21°03ʹ 412² N, 105°47ʹ 248² S, altitude 17m). The nest 
was attached to the roof of a desolate house at an 
uncultivated filed, with a height of 2.5m from the 
ground. 
All cells of the nest were particularly observed, and 
marked with cells which have the present of moth 
cocoons. In conditional laboratory, emerged adult 
moths were reared in non-toxic plastic jars (20 cm 
diameter ´ 12 cm height) by the honey of 50% in 
concentration. Moth larvae were also reared in non-toxic 
plastic jars (10 cm diameter ´ 8 cm height) 
with a number of 5 individuals/jar by larvae and 
pupae of the rice moth Corcyra cephalonica. The 
humidity was, in non-plastic jars, made by the 
absorbent cotton. The shelter of moth larvae and 
moth pupae was with the cells of the nest of the 
paper wasp P. olivaceus. Adult female and adult 
male moths were geminated immediately after they 
emerged. The examination was taken every day 
with a frequency of 2 times/day (9 am and 15 pm). 
Head width of moth larvae were made with the 
ocular micrometer attached to a stereoscopic 
dissecting microscope. The temperature and the 
humidity in the laboratory were automatically 
marked by a Humidity and Temperature Recorder, 
Extech RH520. Pictures were taken by a digital 
camera Canon SD3500 IS.
Pham 91 
RESULTS AND DISCUSSION 
A total of 34 nests of the paper wasp P. olivaceus 
collected from the beginning of January to the end of 
March in 2012 and 2014, only the one had the present 
of the snout moth H. postflava (Fig. 1a). In the world, 
this moth only discovered in Japan, with its parasitism 
on the nest of paper wasp P. jadwigae (Nakatani and 
Yamamoto, 1999) and P. jokahamae (Kato, Yamada, 
Matsuura and Tsukada, 2007a, b). This paper is thus 
the first record for parasitism of H. postflava on the 
nest of the paper wasp P. olivaceus. 
Fig. 1. a) The nest of the paper wasp P. olivaceus parasitized by H. postflava, with the silks on the surface of 
the nest; b) Adult female moth; c) Moth larva; d and e) Moth pupa. 
The nest of P. olivaceus was with 437 cells, 8 cm in 
height, 14 cm of the diameter, and 1.1 cm in length 
of the eccentric peduncle. Of those cells, 25 
contained moth cocoons. In the duration of 9 days 
from 12 to 20 April, 2014, a total of 23 adult moths 
emerged from the nest of P. olivaceus. Of these, 9 
were females and 14 were males. Thus sex ratio of 
this moth (♀:♂) was 1:1.55, and survivorship ratio 
of pupae was 92% ((23:25)*100). Adult moths 
emerge on the beginning of the summer. It suggests 
that moth pupae overwintered on the nest of the 
paper wasp P. olivaceus. Reasons for that: 1) Scarce 
food resources. Because, if moth adults emerge in 
the duration from October to March of next year, it 
is very difficult for them to find the nest of P. 
olivaceus which contains larvae or pupae to lay eggs 
into or near. In this duration, mated females of the 
paper wasp P. olivaceus are hibernating (Pham, 
2014). Or in other words, new nests of this wasp are 
not built in this duration 2) Severe weather 
conditions. Because this is the winter period 
(October - March), and an average temperature is 
under 15°C in Northern Vietnam. 
Head width of moth larvae showed in Fig. 2. 
According to this data, head width of first instar 
larva was 0.2-0.22 mm, and of second instar larva 
0.3-0.4 mm. However, that of third instar larvae and 
over was very difficult to determine due to great 
variation (from 0.4 to 1.4 mm). Kato et al, 2007 
stated that the head width of overwintering moth 
larvae varied greatly between the nests and also 
within some of the nests, and the authors did not 
determine any age of the moth larvae. Thus results 
examined here only define the age of first instar and 
second instar moth larvae. 
The duration of the life cycle of H. postflava was 
variable, from 33 to 49 days, and the total mean 
duration was 40.46±4.96 days (Table 1). Of these, 
eggs 5.72±1.23 days, larvae 22.03±1.75 days, pupae 
8.33±0.99 days, before laying 4.38±1.02 days. The 
duration of immature stages of H. postflava (first 
generation) provided with pupae of the paper wasp 
P. jokahamae in Japan are: egg 8.1±0.8 days, larva 
23.6±1.8 days, pupa 11.4±0.9 days, and life cycle 
56.4±11.7 days (Kato et al. 2007). The difference 
between two these study results is due to some 
ecological features like local climate and food 
available, which could affect every immature stage 
development, the pupal stage is very similar to that 
in their study result. Newly hatched larvae are 
almost no displacement, 4-5 hours then they move 
and forage the food resources. Larvae ate each other 
when deficiency food or greatly individual density 
(10 individuals/jar and over) without eating eggs, 
and often spin the silk to fix the shelter with the 
plastic jar.
Pham 92 
Mature larvae spin the silk cocoon before they are of 
the formation of pupae. Moth larvae usually hide in 
the shelter except for foraging the food. This is one of 
the basic and important habits of this snout moth. 
Because, with this habit, larvae will escape the attack 
of wasps or of other natural enemies. Life time of 
both female moth and male moth was very similar, 
variable from 6 to 9 days, an average 7.76±1.04 days 
to females, and 7.51±1.03 days to males. Most of 
female moths died after laying egg (about 10-12 
hours). With adding on this datum, life-span of the 
snout moth varied from 37 to 53 days. Thus it is 
considered that H. postflava typically completes two 
or three generations per year. 
45 
40 
35 
30 
25 
20 
15 
10 
5 
Fig. 2. Frequency of head width of moth larvae reared under the laboratorial condition. 
Table 1. Life cycle and life time (days, average ± SD (n)) of both female adult and 
male adult of H. postflava. 
Immature stage Mature stage 
Egg Larva Pupa Before 
laying 
Life cycle Life time of 
female 
Life time of 
male 
3-8 
5.72±1.23 
(n=110) 
28.8°C; 
85.4% RH 
20-25 
22.03±1.75 
(n=60) 
31.8°C; 
85.1% RH 
7-10 
8.33±0.99 
(n=40) 
35.3°C; 
83.7% RH 
3-6 
4.38±1.02 
(n=30) 
36.5°C; 
82.3% RH 
33-49 
40.46±4.96 
(n=30) 
33.3°C; 
83.1% RH 
6-9 
7.76±1.04 
(n=31) 
35.2°C; 
83.5%RH 
6-9 
7.51±1.03 
(n=39) 
35.2°C; 
83.5%RH 
Table 2. Survivorship ratio of larva and pupa and sex ratio of H. postflava. 
Larva Pupa Adult 
Number 
Number 
Ratio 
Number 
Number 
Ratio 
observed 
emerged 
(%) 
observed 
emerged 
(%) 
Female Male Ratio 
50 44 88 40 33 82.50 31 39 1: 1.26 
33.8°C; 84.3% RH 35.2°C; 84.1% RH 
Survivorship ratio of larva and pupa of H. postflava 
was 88% and 82.5% respectively (Table 2). In all 
study time, most of moth larvae reared with 
individuals of 1st and 2sd age died after 2-3 days. 
This can be explained the following: Either the habit 
of colony life, it means here they help each other in 
foraging for the food or mechanical impacts in 
experimental manipulations. A total of 70 adult 
moths examined in the laboratory. Of these, 31 were 
females, and 39 were males (Table 2). Hence the sex 
ratio here (♀:♂) was 1:1.26. In comparison with that 
above, it is inconsiderably different. With the 
difference about the ratio between the two genders, it 
can also suggest that there is choice of females to 
males when they mate together. This is one of the 
causes which lead unsuccessful mating of moth pairs 
experimented (showed below). 
In a total of 18 experimented pairs, 3 pairs did not 
lay eggs (3, 6, and 9), 15 pairs dissected still 
remained eggs in the body (Table 3). The following 
causes are to be considered: 1) unmated females; 2) 
rearing space; 3) food to rear immature and adult 
stage (larvae of C. cephalonica and the honey); 4) 
temperature and humidity in the laboratory; or 5) 
unmatured eggs. As for 3 pairs (3, 6 and 9), causes 
of 2, 3, and 4 are rejected due to the other pairs 
(laying eggs). All of such five causes are referred to 
the case of 15 pairs. 
0 
Frequencyy 
Head width (mm)
Pham 93 
Table 3. Data on eggs of H. postflava. 
Pairs Eggs 
laid 
Eggs remained in 
the body 
A total of 
eggs 
Eggs 
hatched 
Rate of hatched eggs 
(%) 
Situation of 
eggs 
1 34 50 84 0 0 C 
2 64 20 84 6 9.4 C 
3 0 83 83 0 - - 
4 20 62 82 3 15 S 
5 80 11 91 66 82.5 C,S 
6 0 88 88 0 - - 
7 84 32 116 0 0 C 
8 73 19 92 0 0 C,S 
9 0 88 88 0 - - 
10 10 78 88 0 0 S 
11 71 10 81 0 0 C,S 
12 55 26 81 42 76.4 C,S 
13 87 11 98 7 8.0 C 
14 25 - - 0 0 S 
15 15 74 89 0 0 C 
16 61 - - 57 93.4 C,S 
17 15 - - 0 0 S 
18 15 74 89 0 0 S 
Mean 39.39 48.40 88.93 10.06 18.98 
C. Clump, S. Single 
Hence, the mean egg total laid was only 39.39 
eggs/pair. The egg total of a female moth ranged 
from 81 to 116 (mean 88.93 eggs). Also this snout 
moth, with the food of pupae of the paper wasp P. 
jokahamae, a female moth lays a mean of 133.9 eggs 
during their mean lifetime of 10.7 days (Kato et al, 
2007a). Thus, the fecundity of H. postflava is much 
dependent on the food and local climate. Rate of 
hatched eggs was very low, ranging from 0 to 93.4% 
(an average of 18.98%/pair). This is also considered 
as such four causes of 1, 3, 4, and 5 above. As for 
situation of eggs, female adults of the moth laid eggs 
singly or in clumps of a few eggs. This datum is the 
same as that reported by Kato et al., (2007a). 
ACKNOWLEDGMENT 
Author is grateful to Dr. Alexey V. Solovyev, 
Ulyanovsk State Pedagogical University for his kind 
help in identifying H. postflava. 
REFERENCES 
Hughes, D.P., Beani, L., Turillazzi, S. and 
Kathirithamby, J. (2003). Prevalence of the 
parasite strepsiptera in Polistes as detected by 
dissection of immature. Insectes Sociaux, 50: 
62-68. 
Kato, N., Yamada, Y.Y., Matsuura, M. and Tsukada, 
M. (2007a). Mating, oviposition, and prey use 
by larvae of Hypsopygia postflava 
(Lepidoptera: Pyralidae), a moth parasitic on 
nests of the paper wasp Polistes jokahamae. 
Japanese Journal of Applied Entomology and 
Zoology, 51(1):45-50. 
Kato, N., Yamada, Y.Y., Matsuura, M. and Tsukada, 
M. (2007b). Life cycle of Hypsopygia postflava 
(Lepidoptera, Pyralidae), a moth parasitic on 
nests of the paper wasp Polistes jokahamae. 
Japanese Journal of Applied Entomology and 
Zoology, 51(2):115-120. 
Lutz, B.G., Strassmann, J.E. & Hughes, C.R. (1984). 
Nest defense by the social wasps, Polistes 
exclamans and P. instabilis (Hymenoptera: 
Vespidae) against the parasitoid, Elasmus polistis 
(Hymenoptera: Chalcidoidae: Eulophidae). 
Entomological News, 95(2): 47-50. 
Nakatani, K. and Yamamoto, H. (1999). Life-cycle 
and hibernation of Hypsopygia postflava 
Hampson Pyralidae, Pyralinae, parasitic to the 
nest of Polistes jadwigae Dalla Torre 
Vespidae. Japan Heterocerists' Journal, 205: 
85-87. 
Pham, H.P. (2014). Hibernation on the nest of the paper 
wasp, Polistes (Gyrostoma) olivaceus (De Geer) 
(Hymenoptera: Vespidae). Biological Forum - An 
International Journal, 6(1): 116-119. 
Phil Rau, (1941). Observations on certain 
lepidopterous and hymenopterous parasites of 
polistes wasps. Annals of the Entomological 
Society of America 34(2): 355-366. 
Stamp, N.E. and Bowers, M.D. (1988). Direct and indirect 
effects of predatory wasps (Polistes sp.: Vespidae) 
on gregarious caterpillars (Hemileuca lucina: 
Saturniidae). Oecologia, 75: 619-624. 
West Eberhard, M.J. (1969). The social biology of 
Polistine wasps. Miscellaneous Publishcations 
Museum of Zoology, University of Michigan, 
140:1-101.

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phong huy pham

  • 1. Biological Forum – An International Journal 6(2): 90-93(2014) ISSN No. (Print): 0975-1130 ISSN No. (Online): 2249-3239 Biology of Hypsopygia postflava (Lepidoptera: Pyralidae), a Snout Moth Parasitic on the Nest of the Paper wasp Polistes olivaceus (Vespidae: Polistes) Phong Huy Pham Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Hanoi, Vietnam. (Corresponding author: Phong Huy Pham) (Received 08 July, 2014, Accepted 08 September, 2014) ABSTRACT: Hypsopygia postflava, a snout moth parasitic on the nest of the paper wasp Polistes olivaceus was reported first time, with studies on its biology. Head width of moth larvae from third instar and over was difficult to specify because of great variety. The duration of life cycle of H. postflava was 40.46±4.96 days, ranging from 33 to 49 days. Life time of both female adult and male adult was equal (in the 6-9 day range). Survivorship ratio was, for larvae 88%, and for pupae 82.5%. Sex ratio of H. postflava in laboratory experiments (♀:♂) was 1: 1.26 in comparison with 1: 1.55 of that of adult moths emerged from the nest of the paper wasp P. olivaceus. The average number of eggs having in the body of the female adult was 88.93. However female adults only laid a mean of 39.39 eggs during their lifetime. Female adults laid eggs singly or in clumps of a few eggs. The mean ratio of hatched eggs was very low (18.98%). Key words: Hypsopygia, Lepidoptera, lifetime, paper wasp, Pyralidae, snout moth INTRODUCTION Accidentally, on March 22, 2014 when I was concentrating on my study on the hibernation of the paper wasp, Polistes olivaceus (Pham, 2014), with field trips in Hanoi, I collected a nest of this wasp that it had strangeness in comparison with any nest which had been collected before. I decided to scrutinize the nest. On April 12, some adult moths emerged. It made me though whether this was one of moths parasitic on the nest of the paper wasp. I had decided to send specimens of the moth to a colleague of mine in Russian and then he informed me that this was a snout moth parasitic on the nest of the paper wasps, with its scientific name Hypsopygia postflava (Hampson, 1893). H. postflava is one of the snout moths belonging to the family Pyralidae, the order Lepidoptera. To date, in the world, studies on biology, habit or bionomics of the species have been only produced in Japan by Nakatani et al., (1999) with its parasite on the nest of Polistes jadwigae, and by Kato et al., (2007a,b) with its parasite on the nest of Polistes jokahamae. Those studies are about the life cycle, hibernation, mating, oviposition, and prey use by larvae of the species. Thus H. postflava is yet poorly studied. In Vietnam, to now, studies on taxonomy, biology, or bionomic of H. postflava belonging to family Pyralidae are yet very poor and still very lack of documents. However, so far I have not yet had a sufficiency of documents to certify that the snout moth H. postflava is a new record for Vietnam. With discovery of the pupae, and of emergence of adults on the nest of the paper wasp P. olivaceus, the present paper is to record its first parasite on the nest of the paper wasp P. olivaceus, with studies on its biology. MATERIALS AND METHODS A nest of the paper wasp P. olivaceus collected at Nghia Do precinct, Cau Giay district, Hanoi, Vietnam (21°03ʹ 412² N, 105°47ʹ 248² S, altitude 17m). The nest was attached to the roof of a desolate house at an uncultivated filed, with a height of 2.5m from the ground. All cells of the nest were particularly observed, and marked with cells which have the present of moth cocoons. In conditional laboratory, emerged adult moths were reared in non-toxic plastic jars (20 cm diameter ´ 12 cm height) by the honey of 50% in concentration. Moth larvae were also reared in non-toxic plastic jars (10 cm diameter ´ 8 cm height) with a number of 5 individuals/jar by larvae and pupae of the rice moth Corcyra cephalonica. The humidity was, in non-plastic jars, made by the absorbent cotton. The shelter of moth larvae and moth pupae was with the cells of the nest of the paper wasp P. olivaceus. Adult female and adult male moths were geminated immediately after they emerged. The examination was taken every day with a frequency of 2 times/day (9 am and 15 pm). Head width of moth larvae were made with the ocular micrometer attached to a stereoscopic dissecting microscope. The temperature and the humidity in the laboratory were automatically marked by a Humidity and Temperature Recorder, Extech RH520. Pictures were taken by a digital camera Canon SD3500 IS.
  • 2. Pham 91 RESULTS AND DISCUSSION A total of 34 nests of the paper wasp P. olivaceus collected from the beginning of January to the end of March in 2012 and 2014, only the one had the present of the snout moth H. postflava (Fig. 1a). In the world, this moth only discovered in Japan, with its parasitism on the nest of paper wasp P. jadwigae (Nakatani and Yamamoto, 1999) and P. jokahamae (Kato, Yamada, Matsuura and Tsukada, 2007a, b). This paper is thus the first record for parasitism of H. postflava on the nest of the paper wasp P. olivaceus. Fig. 1. a) The nest of the paper wasp P. olivaceus parasitized by H. postflava, with the silks on the surface of the nest; b) Adult female moth; c) Moth larva; d and e) Moth pupa. The nest of P. olivaceus was with 437 cells, 8 cm in height, 14 cm of the diameter, and 1.1 cm in length of the eccentric peduncle. Of those cells, 25 contained moth cocoons. In the duration of 9 days from 12 to 20 April, 2014, a total of 23 adult moths emerged from the nest of P. olivaceus. Of these, 9 were females and 14 were males. Thus sex ratio of this moth (♀:♂) was 1:1.55, and survivorship ratio of pupae was 92% ((23:25)*100). Adult moths emerge on the beginning of the summer. It suggests that moth pupae overwintered on the nest of the paper wasp P. olivaceus. Reasons for that: 1) Scarce food resources. Because, if moth adults emerge in the duration from October to March of next year, it is very difficult for them to find the nest of P. olivaceus which contains larvae or pupae to lay eggs into or near. In this duration, mated females of the paper wasp P. olivaceus are hibernating (Pham, 2014). Or in other words, new nests of this wasp are not built in this duration 2) Severe weather conditions. Because this is the winter period (October - March), and an average temperature is under 15°C in Northern Vietnam. Head width of moth larvae showed in Fig. 2. According to this data, head width of first instar larva was 0.2-0.22 mm, and of second instar larva 0.3-0.4 mm. However, that of third instar larvae and over was very difficult to determine due to great variation (from 0.4 to 1.4 mm). Kato et al, 2007 stated that the head width of overwintering moth larvae varied greatly between the nests and also within some of the nests, and the authors did not determine any age of the moth larvae. Thus results examined here only define the age of first instar and second instar moth larvae. The duration of the life cycle of H. postflava was variable, from 33 to 49 days, and the total mean duration was 40.46±4.96 days (Table 1). Of these, eggs 5.72±1.23 days, larvae 22.03±1.75 days, pupae 8.33±0.99 days, before laying 4.38±1.02 days. The duration of immature stages of H. postflava (first generation) provided with pupae of the paper wasp P. jokahamae in Japan are: egg 8.1±0.8 days, larva 23.6±1.8 days, pupa 11.4±0.9 days, and life cycle 56.4±11.7 days (Kato et al. 2007). The difference between two these study results is due to some ecological features like local climate and food available, which could affect every immature stage development, the pupal stage is very similar to that in their study result. Newly hatched larvae are almost no displacement, 4-5 hours then they move and forage the food resources. Larvae ate each other when deficiency food or greatly individual density (10 individuals/jar and over) without eating eggs, and often spin the silk to fix the shelter with the plastic jar.
  • 3. Pham 92 Mature larvae spin the silk cocoon before they are of the formation of pupae. Moth larvae usually hide in the shelter except for foraging the food. This is one of the basic and important habits of this snout moth. Because, with this habit, larvae will escape the attack of wasps or of other natural enemies. Life time of both female moth and male moth was very similar, variable from 6 to 9 days, an average 7.76±1.04 days to females, and 7.51±1.03 days to males. Most of female moths died after laying egg (about 10-12 hours). With adding on this datum, life-span of the snout moth varied from 37 to 53 days. Thus it is considered that H. postflava typically completes two or three generations per year. 45 40 35 30 25 20 15 10 5 Fig. 2. Frequency of head width of moth larvae reared under the laboratorial condition. Table 1. Life cycle and life time (days, average ± SD (n)) of both female adult and male adult of H. postflava. Immature stage Mature stage Egg Larva Pupa Before laying Life cycle Life time of female Life time of male 3-8 5.72±1.23 (n=110) 28.8°C; 85.4% RH 20-25 22.03±1.75 (n=60) 31.8°C; 85.1% RH 7-10 8.33±0.99 (n=40) 35.3°C; 83.7% RH 3-6 4.38±1.02 (n=30) 36.5°C; 82.3% RH 33-49 40.46±4.96 (n=30) 33.3°C; 83.1% RH 6-9 7.76±1.04 (n=31) 35.2°C; 83.5%RH 6-9 7.51±1.03 (n=39) 35.2°C; 83.5%RH Table 2. Survivorship ratio of larva and pupa and sex ratio of H. postflava. Larva Pupa Adult Number Number Ratio Number Number Ratio observed emerged (%) observed emerged (%) Female Male Ratio 50 44 88 40 33 82.50 31 39 1: 1.26 33.8°C; 84.3% RH 35.2°C; 84.1% RH Survivorship ratio of larva and pupa of H. postflava was 88% and 82.5% respectively (Table 2). In all study time, most of moth larvae reared with individuals of 1st and 2sd age died after 2-3 days. This can be explained the following: Either the habit of colony life, it means here they help each other in foraging for the food or mechanical impacts in experimental manipulations. A total of 70 adult moths examined in the laboratory. Of these, 31 were females, and 39 were males (Table 2). Hence the sex ratio here (♀:♂) was 1:1.26. In comparison with that above, it is inconsiderably different. With the difference about the ratio between the two genders, it can also suggest that there is choice of females to males when they mate together. This is one of the causes which lead unsuccessful mating of moth pairs experimented (showed below). In a total of 18 experimented pairs, 3 pairs did not lay eggs (3, 6, and 9), 15 pairs dissected still remained eggs in the body (Table 3). The following causes are to be considered: 1) unmated females; 2) rearing space; 3) food to rear immature and adult stage (larvae of C. cephalonica and the honey); 4) temperature and humidity in the laboratory; or 5) unmatured eggs. As for 3 pairs (3, 6 and 9), causes of 2, 3, and 4 are rejected due to the other pairs (laying eggs). All of such five causes are referred to the case of 15 pairs. 0 Frequencyy Head width (mm)
  • 4. Pham 93 Table 3. Data on eggs of H. postflava. Pairs Eggs laid Eggs remained in the body A total of eggs Eggs hatched Rate of hatched eggs (%) Situation of eggs 1 34 50 84 0 0 C 2 64 20 84 6 9.4 C 3 0 83 83 0 - - 4 20 62 82 3 15 S 5 80 11 91 66 82.5 C,S 6 0 88 88 0 - - 7 84 32 116 0 0 C 8 73 19 92 0 0 C,S 9 0 88 88 0 - - 10 10 78 88 0 0 S 11 71 10 81 0 0 C,S 12 55 26 81 42 76.4 C,S 13 87 11 98 7 8.0 C 14 25 - - 0 0 S 15 15 74 89 0 0 C 16 61 - - 57 93.4 C,S 17 15 - - 0 0 S 18 15 74 89 0 0 S Mean 39.39 48.40 88.93 10.06 18.98 C. Clump, S. Single Hence, the mean egg total laid was only 39.39 eggs/pair. The egg total of a female moth ranged from 81 to 116 (mean 88.93 eggs). Also this snout moth, with the food of pupae of the paper wasp P. jokahamae, a female moth lays a mean of 133.9 eggs during their mean lifetime of 10.7 days (Kato et al, 2007a). Thus, the fecundity of H. postflava is much dependent on the food and local climate. Rate of hatched eggs was very low, ranging from 0 to 93.4% (an average of 18.98%/pair). This is also considered as such four causes of 1, 3, 4, and 5 above. As for situation of eggs, female adults of the moth laid eggs singly or in clumps of a few eggs. This datum is the same as that reported by Kato et al., (2007a). ACKNOWLEDGMENT Author is grateful to Dr. Alexey V. Solovyev, Ulyanovsk State Pedagogical University for his kind help in identifying H. postflava. REFERENCES Hughes, D.P., Beani, L., Turillazzi, S. and Kathirithamby, J. (2003). Prevalence of the parasite strepsiptera in Polistes as detected by dissection of immature. Insectes Sociaux, 50: 62-68. Kato, N., Yamada, Y.Y., Matsuura, M. and Tsukada, M. (2007a). Mating, oviposition, and prey use by larvae of Hypsopygia postflava (Lepidoptera: Pyralidae), a moth parasitic on nests of the paper wasp Polistes jokahamae. Japanese Journal of Applied Entomology and Zoology, 51(1):45-50. Kato, N., Yamada, Y.Y., Matsuura, M. and Tsukada, M. (2007b). Life cycle of Hypsopygia postflava (Lepidoptera, Pyralidae), a moth parasitic on nests of the paper wasp Polistes jokahamae. Japanese Journal of Applied Entomology and Zoology, 51(2):115-120. Lutz, B.G., Strassmann, J.E. & Hughes, C.R. (1984). Nest defense by the social wasps, Polistes exclamans and P. instabilis (Hymenoptera: Vespidae) against the parasitoid, Elasmus polistis (Hymenoptera: Chalcidoidae: Eulophidae). Entomological News, 95(2): 47-50. Nakatani, K. and Yamamoto, H. (1999). Life-cycle and hibernation of Hypsopygia postflava Hampson Pyralidae, Pyralinae, parasitic to the nest of Polistes jadwigae Dalla Torre Vespidae. Japan Heterocerists' Journal, 205: 85-87. Pham, H.P. (2014). Hibernation on the nest of the paper wasp, Polistes (Gyrostoma) olivaceus (De Geer) (Hymenoptera: Vespidae). Biological Forum - An International Journal, 6(1): 116-119. Phil Rau, (1941). Observations on certain lepidopterous and hymenopterous parasites of polistes wasps. Annals of the Entomological Society of America 34(2): 355-366. Stamp, N.E. and Bowers, M.D. (1988). Direct and indirect effects of predatory wasps (Polistes sp.: Vespidae) on gregarious caterpillars (Hemileuca lucina: Saturniidae). Oecologia, 75: 619-624. West Eberhard, M.J. (1969). The social biology of Polistine wasps. Miscellaneous Publishcations Museum of Zoology, University of Michigan, 140:1-101.