1. Introduction
Biological control by inundated releases of the parasitoids is a promising strategy for combating stored-product insects due to increasing negative effects resulting from a long-term use of conventional insecticides, such as insecticide residues in food products, environmental contamination, and so forth.
Habrobracon hebetor Say (Hymenoptera: Braconidae) is a highly cosmopolitan, gregarious ecto-parasitoid of a variety of Lepidopterous larvae occurring in grain storage spaces, such as
Plodia interpunctella (Hübner),
Ephestia elutella (Hübner),
Anagasta kuehniella Zeller, and
Corcyra cephalonica (Stainton), which frequently infest stored cereals, beans, oilseeds, rice, wheat, dried fruits, and medicinal materials [
1,
2,
3].
The large-scale rearing of parasitoids is crucial for the successful implementation of biological control. Host species significantly affect the growth and development of parasitoids [
4]. Therefore, screening the most suitable host species for
H. hebetor mass rearing is imperative to effectively control Lepidopterous larvae occurring in grain storage spaces. Dabhi et al. [
5] evaluated the biology of
H. hebetor on seven Lepidopteran larvae,
Sitotroga cerealella (Olivier),
C. cephalonica (Stainton),
Galleria mellonella Linn, and
Earias vittella (Fab.) at ambient temperatures.
Corcyra cephalonica was the best host for
H. hebetor mass rearing among the tested Lepidopteran larvae.
Ephestia elutella is the most destructive Lepidopterous pest during tobacco storage.
Ephestia elutella larvae frequently cause serious loss by feeding stored tobacco and its products [
6]. Meanwhile,
E. elutella larvae feeding may result in increasing moisture and temperature which is in favor of mold development in stored tobacco and its products [
7].
Habrobracon hebetor can effectively attack
E. elutella larvae. Parasitic rate of
H. hebetor on
E. elutella larvae was more than 70% at the peak period of their host larvae occurrence in tobacco storage warehouse in Guizhou, China, from mid-late June to mid-late August [
8]. Therefore,
H. hebetor has great potential for controlling
E. elutella.
Habrobracon hebetor is sensitive to changes in environmental temperature, which is an important factor affecting the growth and development of insects [
9]. There have been many studies on the effects of temperature on the growth and development of parasitoids. The developmental duration and adult life span of
Microplitis similis Lyle (Hymenoptera: Braconidae) decrease with increasing temperature from 18 °C to 33 °C, and the maximum fecundity appears at 27 °C and 30 °C [
10].
Brachymeria lasus Walker (Hymenoptera: Chalcididae) can parasitize pupae of
E. elutella. Its developmental period decreased, and its development rate increased with increasing temperature from 16 °C to 32 °C [
8,
11]. The developmental starting temperatures of
H. hebetor eggs, larvae, and pupae are 10.12, 13.24, and 10.60 °C, respectively [
12]. Egg hatching rate of
Anisopteromalus calandra (Howard) (Hymenoptera: Pteromalidae) first increased and then decreased with increasing temperature. The highest hatching rate of
A. calandra reached 88.67% at 25 °C. The developmental duration and adult life span of
A. calandra decreased with increasing ambient temperature [
13]. The longest development duration of
H. hebetor larvae on
G. mellonella larvae was 6.60 d at 20 °C [
14].
However, the growth and development of H. hebetor on E. elutella larvae is meagre so far, which is of great significance for the large-scale breeding of H. hebetor and its efficient utilization for controlling E. elutella. Thus, the present study aims to investigate the effects of different temperatures (15, 20, 25, 30, and 35 °C) on the growth and development of H. hebetor on E. elutella larvae.
2. Materials and Methods
2.1. Insects
Habrobracon hebetor was obtained from Guangdong Institute of Grain Science (Guangzhou, China) and reared on 5th instar larvae of E. elutella in the laboratory at the Institute of Stored Product Insects of Henan University of Technology, Zhengzhou, China. E. elutella was maintained on sterilized artificial diet (wheat bran/glycerin/honey/distilled water (87:5:5:3)). To obtain 5th instar larvae of E. elutella for the following experiments, E. elutella adults were allowed to oviposit on the artificial diet for 3 d, and then, the artificial diet was kept in an incubation chamber for 35 d at 30 ± 2 °C, 75 ± 5% relative humidity (RH), and a photoperiod of 12:12 h (L:D).
2.2. Temperature-Dependent Longevity and Fecundity of Adult H. hebetor
Groups of 15 E. elutella 5th instar larvae were placed in a plastic box (a bottom diameter of 5.5 cm, a top diameter of 7.3 cm, and a height of 3.5 cm, containing about 3 g sterilized artificial diet). The boxes were, respectively, maintained at 15, 20, 25, 30, and 35 °C in incubators, and one pair (male/female) of H. hebetor (1–2-day-old) adults was introduced into each box. After 24 h, the H. hebetor adults were transferred into a new plastic box containing another group of 15 5th instar larvae of E. elutella. The number of eggs laid by the H. hebetor on the previous group of 15 E. elutella 5th instar larvae was checked under a microscope. Then, the previous group of 15 E. elutella 5th instar larvae with H. hebetor eggs were placed in the original plastic box at 30 ± 2 °C, 75 ± 5% relative humidity (RH), and a photoperiod of 12:12 h (L:D). This operation process was repeated every 24 h until the death of the H. hebetor. The total number of eggs, the emergence rate of H. hebetor in each plastic box, the percentage of female offspring, and the life span of the offspring males and females were recorded. Ten replicates were conducted.
2.3. Temperature-Dependent Survival and Development Time of H. hebetor
Each four pairs of H. hebetor adults (female/male = 1:1, 1–2-day-old) were released into one plastic box containing 25 5th instar larvae of E. elutella. The H. hebetor adults were removed after 24 h, and 30 eggs of H. hebetor on E. elutella larvae were obtained under a microscope (there were 3–6 eggs of H. hebetor on one E. elutella larva). Then, the plastic boxes were maintained at 15, 20, 25, 30, and 35 °C, and 70 ± 5% RH, respectively. The development of H. hebetor eggs was observed until adult emergence at 6:00, 14:00, and 22:00 every day. The egg hatchability, egg developmental duration, larval development duration and survival rate, pupal development duration, emergence rate, net productive rate, innate rate of increase, and population doubling time of H. hebetor were calculated. Fifteen replicates were conducted. A total of 2250 eggs (30 eggs per treatment × 5 temperatures × 15 replicates = 2250 eggs) were used for the experiment.
2.4. Data Analysis
Temperature and sex (male and female) were used as independent variables, and the adult longevity was used as a response variable for two-way analysis of variance (ANOVA). Temperature was used as an independent variable, and the fecundity was used as a response variable for one-way analysis of variance (ANOVA). Temperature and life stage were used as independent variables, and egg hatchability, survival rate of larvae and pupae of H. hebetor, and developmental duration were used as response variables for two-way analysis of variance (ANOVA). The adult longevity, fecundity, and developmental duration of H. hebetor were transformed to log10(x + 1) scale, and survival rate and egg hatchability were transformed to arcsine square-root values before being subjected to ANOVA analysis for homogeneity of variances with Tukey’s test for mean separation at p < 0.05. The equations for the linear regression between temperature (T) and developmental rate (V) for each life stage of H. hebetor at different temperatures were defined. SPSS23.0 was used for data analysis.
The developmental duration (
N) of eggs at each temperature was converted into the developmental rate (
V = 1/
N), and the developmental threshold temperature (
C) and effective accumulated temperature (
K) were calculated using the following equations.
In Equations (1)–(5), C represents the developmental threshold temperature, K is the effective accumulated temperature, n is the number of insects, T′ is the theoretical value of temperature, T is the test temperature, and SC and SK are the standard errors of the developmental threshold temperatures (C) and effective accumulated temperatures (K).
A predictive equation of the development time of various developmental stages of
H. hebetor was established as follows:
The exact value of intrinsic increase rate (
rm) was calculated using stepwise approximation method.
In Equation (7), x represents the median age, where is the mean survival probability from age x to x + 1, and is the number of female offspring produced per female in the interval x.
4. Discussion
The present results showed that
H. hebetor could complete development from egg to adult on
E. elutella larvae in the temperature range of 15 °C to 35 °C, and the generation duration of
H. hebetor gradually decreased with increasing temperature. The emergence rate and life span of
H. hebetor was similar to Zeng et al. and Tian et al. [
14,
15].
The total number of eggs laid by
H. hebetor reached the maximum of 192.39 at 30 °C. This was also similar to previous research results [
12,
16,
17], where
G. mellonella larvae and
P. interpunctella larvae were used as hosts. However, the maximum emergence rate of
H. hebetor reached 70.08% when
E. elutella larvae were used as hosts in the present study, which was significantly higher than (35.87%) when
G. mellonella larvae were used as hosts in Tian et al. [
14]. When
Cadra cautella larvae were used as hosts at 27 ± 2 °C, the egg hatchability, pupation rate, and adult emergence rate were more than 95% [
18].
Net reproductive rate refers to the ability of female individuals in a population to give birth to the total number of new female individuals within a given time. Intrinsic increase rate refers to the maximum increase capacity (
rm) of a population that can be observed under unrestricted conditions, such as being able to eliminate adverse weather conditions, provide ideal food conditions, and eliminate predators and diseases. Both can reflect the increased potential of a population. The net reproductive rate and intrinsic increase rate of
H. hebetor reached the maximum at 30 and 35 °C, which is consistent with Golizadeh et al. [
19] who reared
H. hebetor on
A. kuehniella larvae. The optimum temperature for the growth and development of
H. hebetor is 30 °C [
14,
19]. Taking into account factors such as the total number of eggs laid, egg hatchability, number of emerged adults, emergence ratio, percentage of female offspring, innate rate of increase, and net reproductive rate, it is believed that optimal temperature for rearing of
H. hebetor on
E. elutella larvae is 30 °C in the current study.
This current study was carried out at constant temperatures (15, 20, 25, 30, and 35 °C), 75 ± 5% RH, and a photoperiod of 12:12 h (L:D), and the life parameters of H. hebetor under ambient conditions require further investigation, which is more in line with the actual application scenario of biological control. In addition, the present results provide more choices for determining suitable hosts for H. hebetor mass rearing. Especially, E. elutella is the most destructive Lepidopterous pest insect in tobacco storage spaces, and it is very interesting to investigate if H. hebetor reared on E. elutella larvae has stronger potential in controlling E. elutella infestation.
In addition, integrated pest management (IPM) has become the main direction of pest control. IPM emphasizes the coordinated application of multiple pest control methods [
20,
21,
22]. Combining the application of
H. hebetor and
Metarhizium anisopliae (Metsch.) is compatible for effectively controlling
Ephestia kuehniella Zeller larvae [
23,
24]. The combined application of
Heterorhabditis indica (Rhabditida: Heterorhabditidae) and
H. hebetor may be beneficial for the control of
P. interpunctella [
25]. Carifend
®, an alpha-cypermethrin-coated polyester net, provides a satisfactory level of protection to stored tobacco against
Ephestia elutella [
26].
Ephestia kuehniella exhibits different behavioral preferences towards surfaces treated with diatomaceous earth (DE) and spinosad formulations [
27]. Thus, whether the combination of
H. hebetor and other control measures, such as physical control, chemical control, or other biological control methods, can effectively control
E. elutella should be investigated in the future.
5. Conclusions
In conclusion, H. hebetor could complete growth and development when E. elutella larvae were used as hosts, and the developmental duration decreased with increasing temperature at 15, 20, 25, 30, and 35 °C. The development threshold temperatures of H. hebetor eggs, larvae, pupae, and egg-to-adult stages were 13.89, 6.39, 9.24, and 9.29 °C, and the effective accumulated temperatures were 23.33, 46.40, 142.68, and 240.31 °C·d, respectively. The total number of eggs laid by H. hebetor, the hatching rate of H. hebetor eggs, and the percentage of female offspring reached the maximum of 192.39, 83.89%, and 74.04% at 30 °C, respectively. There was no significant difference in pupal survival rate in the temperature range of 15 °C to 35 °C. At 30 °C, the pre-oviposition duration of H. hebetor was the shortest (0.87 d). The innate rate of increase and net reproductive rate reached the maximum at 30 °C. Therefore, the optimal rearing temperature of H. hebetor was 30 °C. The present results are in favor of the large-scale rearing of H. hebetor using E. elutella larvae as hosts for controlling Lepidopterous pests in practice.