Keywords
Noctuids, Insects, Diet, Treatments, Trials
This article is included in the Agriculture, Food and Nutrition gateway.
The research focused on evaluating the biological and reproductive parameters of the species Spodoptera sunia with the introduction of field genetic material, in the Noctuid Insect Breeding Laboratory.
The experiment consisted of three treatments and three repetitions involving 30 individuals each. Field-collected S. sunia population was reared in the laboratory under semi-controlled conditions of temperature and humidity for three generations. The progeny of the third generation was crossed with the laboratory population and the resulting progeny was observed for growth and reproductive fitness.
The results revealed that the hybrid progeny (T3) has a sex ratio (F: M) of 0.82, as against 1.22 and 0.76 observed in the field (T1) and lab populations (T2) respectively. The T1 females oviposited 196 egg masses as against 160 and 59 egg masses by T3 and T2 females respectively. The larval growth was more in hybrid progeny with shorter larval duration. However, no variation was observed in the incubation and pupal periods.
Since the most optimal results were obtained in T2 and T3, it is recommended to introduce genetic material every six months to maintain a good laboratory population of the insect host under study and better breeding of its natural enemies.
Noctuids, Insects, Diet, Treatments, Trials
In this revised version of our article, we have implemented several significant improvements based on the valuable feedback from the reviewers. The major differences between this version and the previously published one are as follows:
Title and Species Naming: The title now includes the full species name "Spodoptera sunia" without abbreviations, adhering to taxonomic formatting guidelines. Additionally, the Order and Family names are correctly formatted without italics.
Abstract: We have made necessary revisions to the abstract, removing superfluous information and improving the clarity of our study's focus.
Methods Section: We have enhanced the clarity of the methodology, providing a more comprehensive description of the protocols followed, addressing grammatical issues, and eliminating redundancies.
Statistical Validation: The statistical tests used have been clarified, ensuring that they are accurately applied and described. Unnecessary details and formulae have been removed.
Tables and Figures: Legends, labels, and data in the tables and figures have been revised for accuracy and consistency, and problematic figures have been corrected.
Conclusions Section: The conclusions have been refined for clarity and accuracy.
Grammar and Language: Extensive work has gone into refining the manuscript's grammar and language to enhance readability and eliminate errors.
These revisions reflect our commitment to addressing the reviewers' comments and ensuring the overall quality of our research. We believe that these changes significantly improve the manuscript and make it more suitable for publication.
See the authors' detailed response to the review by Hend Omar Mohamed
See the authors' detailed response to the review by María L Russo and Florencia Vianna
See the authors' detailed response to the review by SB Suby
In agricultural production, producers have been grappling with pest control, with particular emphasis on pests exhibiting high adaptability. Notably, phytophagous insects have proven to be challenging adversaries in this regard (Brunetti et al., 2022; Saldamando and Marquez, 2012; Extremera et al., 2004; Pérez et al., 2003; Armstrong, 1994). It is worth mentioning that the genus Spodoptera sp. (Guenée) (Lepidoptera: Noctuidae) is a prominent member of the Noctuidae family, with geographical presence spanning across North America, Latin America, France, Italy, the Black Sea region, the Balkans, England, North and Southern Africa, the Middle East, the Iberian Peninsula, and Germany (Kergoat et al., 2021; Zelaya et al., 2022).
Due to its omnivorous nature, S. sunia is widespread and affects various crops. Ministry of Agriculture, Livestock, Rural Development, Fisheries and Food (SAGARPA, 2002) mentions in the case of Mexico that S. sunia is considered a pest of economic importance that periodically affects essential crops. To control pest, many laboratories produce and reproduce these organisms in order to reduce and control the population of pests in crops, some genera are Trichogramma, Spalangia Telenomus, Cochliomyia, Ceratitis, Baculovirus and Nomuraea rileyi (predators and parasitoids, viruses and entomopathogenic fungi) (Jiménez, 2022; Badii & Abreu, 2006).
In the National Autonomous University of Nicaragua, Leon (UNAN-Leon), the Insect Breeding Laboratory began the reproduction of insects in the 80s, establishing quality controls in breeding, in such a way that the life tables allow determining the biological parameters and reproduction of the insect’s species.
In addition, due of their significance as hosts for the nuclear polyhedrosis virus (NPV), which is considered a biological control agent for pest insects in economically important crops, they play a crucial role in preventing environmental contamination, safeguarding, human health, and protecting other vertebrates (Haase et al., 2015; Romero Gutierrez and Cruz Reyes, 2011; Carrillo et al., 2003; Muentes, 2000).
The study focused on characterizing the biological parameters of the species S. sunia with the introduction of field genetic material (cross-species) at the Noctuid Insect Breeding Laboratory, Biological Control Agent Production and Reproduction Research Center (CIRCB), UNAN-León.
Ultimately, the subject of study becomes important given the need to study these parameters and the performance of the species S. sunia with the introduction of new natural genetic material (cross-species) to improve breeding and maintain optimal parameters (Raj et al., 2022; Rizo, 1994; Rizo et al., 1994; Passoa, 1991).
The research was carried out at the Noctuid Insect Breeding Laboratory (CIRCB), UNAN-León Agricultural Campus, (12°07′02.8″N 86°14′09.6″W). The environmental conditions were maintained under temperatures between 25°C and 27°C and a relative humidity of 60%.
The effect of crossing specimens of the species S. sunia was characterized in order to strengthen the genetic material of the breeding of S. sunia insects used as a host in the production of the NPV (Vásquez et al., 2002; Salinas-Sánchez et al., 2020).
The protocol used began with the collection of Spodoptera sunia in the field. The Sébaco area located in the coordinates (12°52′42.4″N 86°05′29.3″W) was selected. The full protocol can be found on protocols.io (Real-Baca and Zuniga-Gonzalez, 2022a). The selection criteria was that it is an area that produces vegetables and where the presence of noctuid insects is more representative, just as the producers in the area demand NPV products for the control of pest insects. After the collection, they were stored in the Noctuid Insect Breeding Laboratory (CIRCB), a quarantine period of up to three generations was spent. The soybean-based diet was prepared. This diet underwent a sterilization process and was supplemented with vitamins and antibiotics.
In the assembly of the bioassays, two stages were considered (adults and larval length). The treatments were: T1: S. sunia species brought from the field, T2: S. sunia species from the Noctuid Insect Breeding Laboratory (CIRCB), T3: S. sunia species Crossing (field-laboratory).
250 field larvae were collected, which were subjected to a quarantine process for three generations, this to eliminate any contaminants from the field. Of these 250 larvae, a mortality of 75 larvae (30%) was obtained. This mortality was due to bacterial infection. Of the remaining 175, 10 had a poor pupal formation and 25 failed to exit the capsule, therefore, they did not reach the adult stage, leaving 140 adults at the end. After passing the three generations, approximately 200 pupae were obtained, of which 60 pupae were taken for the Field (T1) and Laboratory (T2) treatments, which were sexed and weighed to start the assembly of the test. Treatments were as follows:
• Treatment 1: S. sunia species brought from the field
• Treatment 2: Species of S. sunia from the Breeding Laboratory
• Treatment 3: S. sunia species Crossing (field-laboratory)
In each repetition, 40 larvae were selected for a total of 120 larvae per treatment, resulting in 360 larvae in total. A six-day-old larva was deposited per four-ounce cup with a 2-cm square piece of diet, with the help of a tweezers the larvae were placed on the millimeter sheet to measure the length of each larva, and they were weighed daily on a Denver Instrument Co Serial No 3570 Analytical Balance. Also, the number of males and females per egg laying cage (replication) was considered. The following variables were evaluated:
• Larvae length: Each larva was placed on a millimeter sheet and the length measured in mm was observed.
• Hatching percentage: The number of eggs that hatched was counted visually.
• Weight of larvae: Larvae were weighed on a Denver Instrument Co Denver Analytical Balance, Cool, Serial No 3570.
• Weight of pupae: The pupae were weighed on a Denver Instrument Co Denver Analytical Balance, Cool, Serial No 3570.
• Sex of pupae: The abdominal part of the pupae was observed with the help of a Westover Scientific stereoscope (Rizo et al., 1994).
• Life cycle: The days it took in each of the larval stages were counted.
The data processing was conducted using IBM SPSS Statistics software (RRID:SCR_016479) v.21. Statistical analysis included the Student’s t-test, Kolmogorov-Smirnov test (K-S), Shapiro–Wilk test (W) (normality tests), Mann–Whitney U test and Lilliefors test (Shapiro and Wilk, 1965; Sánchez Turcios, 2015; Torres et al., 2012).
Student’s t-test used to compare the two treatments and determine if there are significant differences between the means of these groups. And it was also, used to evaluate whether the samples from two groups are statistically different in terms of their population mean (Raju, 2005; Malais and Ravensberg, 1992).
K-S test was used to verify the normality of the distribution between treatments (bioassays), equation 1 (Massey, 1951).
The W test was used to contrast the normality of a data set of the combined treatments, equation 2 (Shapiro, 1965).
Mann–Whitney U test was used to check the heterogeneity of two ordinal treatments, equation 3. The starting point is:
Treatment data is autonomous.
The data are ordinal or continuous variables.
Under H0, the initial distribution is the same for both treatments: P(T1 > T2) = P(T2 > T1)
In the first H1, the value of one type of treatment tends to exceed the other: P(T1 > T2) + 0.5 P(T1 = T2) > 0.5.
Where T1 and T2 are the sizes of each treatment; R1 and R2 are the rank sum of bioassay 1 and 2 observations, respectively (the sum of the relative position of each individual in the treatment). The U statistic is defined as the minimum of U1 and U2 (Turcios, 2015).
Lilliefors test is a normality test based on the K-S test. It was used to test H0 that the data come from a normally distributed population (Lilliefors, 1967, 1969).
Table 1 shows the descriptive statistics of the data used at the time of establishing the bioassays. Table 1 provides a concise overview of the final weight (in milligrams) for each of the three treatments in the bioassay. The data is based on a sample size of 60 for each treatment. On average, the final weight for T1 was 0.21 mg with a standard deviation of 0.04 mg and a mean standard error of 0.01. Similarly, T2 exhibited an average final weight of 0.23 mg, with a standard deviation of 0.05 mg and a mean standard error of 0.01. T3 had an average final weight of 0.20 mg, a standard deviation of 0.04 mg, and a mean standard error of 0.01. These statistics offer valuable insights into the variability and central tendency of the final weight data across the different treatments in the study.
The research set out to study the biological and reproductive characteristics of S. sunia (Malais and Ravensberg, 1992), known as (Guen) = (Xylomige ssunia) called cutworm, tiger worm, leathery worm. The characterized variables were length and weight of larvae, hatching percentage, weight and sex of pupae (Parra et al., 2022; Peterson et al., 2022; Barcellos, 2022; Machado et al., 2020).
Figure 1 (Real-Baca and Zuniga-Gonzalez, 2022b) presents the length (mm) of the larvae in the different treatments. It was observed that the treatments begin to have changes in their length after day 10. The three treatments reached their greatest length at 13 days, it was noted that T3 reached the greatest length (30 mm).
Table 2 presents the results of the normality tests for length (mm) and weight (mg) of the larvae during the larval stage across different treatment combinations. These tests are essential to assess whether the data conforms to a normal distribution, which is a crucial assumption for various statistical analyses. The Kolmogorov-Smirnov and Shapiro-Wilk tests were applied, and the obtained p-values for all combinations were extremely low (less than 0.05), leading to the rejection of the null hypothesis and confirming that the data indeed follow a normal distribution. These findings provide a solid foundation for subsequent statistical analyses.
Normality test | |||||||
---|---|---|---|---|---|---|---|
Variables | Treatments | Kolmogorov-Smirnova | Shapiro-Wilk | ||||
Statistical | gl | Sig. | Statistical | Gl | Sig. | ||
Length in mm | Combination T1-T2 | 0.16 | 1,500 | 0 | 0.91 | 1,500 | 0 |
Weight in mg | 0.43 | 1,500 | 0 | 0.08 | 1,500 | 0 | |
Length in mm | Combination T1-T3 | 0.13 | 1,320 | 0 | 0.94 | 1,320 | 0 |
Weight in mg | 0.42 | 1,320 | 0 | 0.09 | 1,320 | 0 |
In the Mann–Whitney U test, it was obtained that the significance of the treatments T2-T3, and T3-T1 was 0.000 less than 0.05, so the H0 is rejected, that is, there is a significant difference in terms of the length of the larvae, in the case of treatments T2-T3 the significance was 0.057 greater than 0.05, in terms of larval weight the significance was 0.098 greater than 0.05, so we accept the H0 of equality between the treatments, that is that there is no significant difference in terms of the length and weight of the larvae (Table 3).
Statistical testa | |||
---|---|---|---|
Statistical test | Treatments | Length in mm | Weight in mg |
Mann-Whitney | Combination T2-T3 | 265438.5 | 267508 |
Wilcoxon | 547063.5 | 549133 | |
Z | -1.907 | -1.656 | |
Sig. asymptotic (bilateral) | 0.057 | 0.098 | |
Mann-Whitney | Combination T3-T1 | 172098 | 169339 |
Wilcoxon | 453723 | 450964 | |
Z | -6.111 | -6.51 | |
Sig. asymptotic (bilateral) | 0 | 0 |
After day 13 in all treatments, a decrease in length was observed because in that week from day 16 to day 22 the environmental conditions were not appropriate. Treatments T2-T3 reached their greatest length on day 23 with 31 mm and later descended their length to enter the pre-pupal stage.
The best larval development was in the T3 treatment with 30 mm because this treatment contains genes from Laboratory larvae, being more adapted to the artificial Soya diet. In the Laboratory treatment, larvae with 27 mm are obtained, this is because it is adapted to the conditions and food, continuing the T3 larvae with 27 mm because it is not adapted to these controlled conditions, but to natural conditions.
Romero Gutierrez and Cruz Reyes (2011) obtained an average length in the first instar of 0.5 cm, reaching its maximum length at approximately 14 days with a length of 2.5 cm (25 mm), this confirms the results obtained with a length of 27 mm for T1 and T2 treatment, the T3 treatment reached a length of 30 mm, this indicates a genetic improvement when introducing field material and mixing it with the laboratory material. For the T3 treatment, its larval growth ends at 18 days, therefore, its larval development was faster.
Figure 2 presents the weight of the larvae (mg). Treatment T3 on day 18 reached its highest weight (0.42 mg), this treatment being the one that reached the highest weight, and then began to lose its weight to enter the pre-pupal stage. The T1 treatment reaches a weight of 0.33 mg at 19 days and 0.30 mg at 20 days in the T2 treatment.
Romero Gutierrez and Cruz Reyes (2011) obtained weights of 0.25 gr (0.250 mg) and in our study it was 0.33 mg in the T1 and 0.30 mg for T2, in the case of T3 it was 0.43 mg. Thus, confirming that there is a difference in the crossover and field treatment since they obtained a greater weight; as soon as the laboratory treatment was similar to the weight of its study, this is due to the genetic deterioration found in the offspring.
Table 4 and Table 5 show the results of the number of eggs in the different treatments. In the T1 treatment they oviposited nine days, obtaining a total of 23,354 eggs that corresponds approximately between 10 to 450 eggs for each mass with a total of 196 egg masses. The T2 treatment oviposited seven days for a total of 4,456 eggs ranging from four to 400 eggs each mass with a total of 59 egg masses, and the T3 treatment obtained the highest number of eggs, 18,025 eggs with nine days of oviposition with a number ranging from 15 to 450 eggs per egg mass for a total of 160 egg masses.
Day | T1 | T2 | T3 |
---|---|---|---|
1 | |||
2 | |||
3 | 1744 | 1186 | |
4 | 2972 | 2903 | |
5 | 5670 | 3416 | |
6 | 4439 | 373 | 3124 |
7 | 2689 | 633 | 2442 |
8 | 2670 | 1035 | 2585 |
9 | 2703 | 1392 | 1482 |
10 | 665 | 749 | 886 |
11 | 2 | 257 | 1 |
12 | 0 | 17 | 0 |
13 | 0 |
In the T3 and T1 treatment, oviposition began after three days, but not in the T2 treatment, this was due to the fact that the fertility of the adult drops due to the fact that they are crosses between the same family, as inbreeding increases, insects decrease their performance (Martinez, 1994; Bárcenas, 1997). The most used variables are fecundity, egg viability, development time, body size, survival and efficiency (Huettel, 1976; Moore et al., 1985; Smith et al., 1996). This confirms that it is important to introduce field material to the laboratory to obtain a better fertility and thus obtain a better reproduction in the breeding of insects.
The normality of the data for the final weight in mg was done with the K-S test, the significance was 0.200 greater than 0.05, so H0 was accepted, likewise the data follow a normal distribution (Table 6), for the different combinations of treatments, the parametric Student’s T-test was calculated for independent samples of the treatments (T2-T3, T3-T1, T2-T1). It was observed that the homogeneity of variance is fulfilled because the significance is greater than 0.05. In the Student’s T-test, a significance of 0.03 less than 0.05 was obtained, it was concluded that there is a significant difference between the final weight in mg of S. sunia of T2 and T1 (Table 7).
Treatment combinations | Kolmogorov-Smirnova | Shapiro-Wilk | ||||
---|---|---|---|---|---|---|
Statistical | Gl | Sig. | Statistical | gl | Sig. | |
T2-T1 | 0.044 | 120 | .200* | 0.97 | 120 | 0.02 |
T3-T1 | 0.059 | 120 | .200* | 0.98 | 120 | 0.14 |
T2-T1 | 0.048 | 120 | .200* | 0.97 | 120 | 0.02 |
Treatment combinations | Variance | Levene's test of equality of variances | Student's T-test for equality of means | 95% confidence interval of the difference | ||||||
---|---|---|---|---|---|---|---|---|---|---|
F | Sig. | t | gl | Sig. (bilateral) | Difference of means | Difference of means | ||||
Lower | Higher | |||||||||
T2-T3 | *σ | 1.63 | 0.21 | 3.36 | 118 | 0.001 | 0.03 | 0.01 | 0.01 | 0.04 |
**σ | 3.36 | 112.35 | 0.001 | 0.03 | 0.01 | 0.01 | 0.04 | |||
T3-T1 | *σ | 0.15 | 0.7 | -1.32 | 118 | 0.19 | -0.01 | 0.01 | -0.02 | 0.00 |
**σ | -1.32 | 117.85 | 0.19 | -0.01 | 0.01 | -0.02 | 0.01 | |||
T2-T1 | *σ | 0.15 | 0.7 | -1.32 | 118 | 0.19 | -0.01 | 0.01 | -0.02 | 0.01 |
**σ | -1.32 | 117.85 | 0.19 | -0.01 | 0.01 | -0.02 | 0.01 |
In the Student’s T-test, a significance of 0.001 less than 0.05 was obtained, it was concluded that there is a significant difference between the final weight in mg of S. sunia in the Laboratory treatment and the Crossing. In the Student’s T-test, a significance of 0.190 greater than 0.05 was obtained, it was concluded that there is no significant difference between the final weight in mg of S. sunia of T3 and T1.
Table 8 shows the number of pupae of the populations of S. sunia from treatment T2, which obtained a total of 60 pupae, of which 34 males and 26 females pupae, for a sex ratio of 0.7:1. Treatment T1 obtained a total of 60 pupae, 28 females and 32 males for a sex ratio of 0.8:1 and in treatment T3 a total of 60 pupae, 33 females and 27 males, and a sex ratio of 1.2 were obtained: 1. This indicates that the proportion for T2 and T3 was not optimal and that of T3 was the most optimal, this is favorable considering that more female pupae than male pupae are needed in the laboratory for greater reproduction and better conditions.
Average weight and sex of initial pupae | ||||
---|---|---|---|---|
Treatments | Number of pupae | Weight (mg) | ||
Females | Males | Females | Males | |
T1 | 28 | 32 | 0.211 | 0.20 |
T2 | 26 | 34 | 0.24 | 0.22 |
T3 | 33 | 27 | 0.22 | 0.21 |
With respect to weight, we observed that the female S. sunia pupae in the three treatments were larger than the males. The T2 treatment had a higher weight (0.2401), but not the T3 and T1 treatments (0.2197 and 0.2112), respectively.
Figure 3 presents the average number of days in each stage of development of the species S. sunia in the three treatments. In the egg and pupal stages, the three treatments had no difference in days. In the larval stage for treatment T2 and T1 there was no difference (24 days), but not for treatment T3, which presented a small difference (18 days). In the adult stage, the T2 treatment obtained 10 days and in the T1 and T3 treatments they obtained a difference of two days (12 days).
Romero Gutierrez and Cruz Reyes (2011) and Delgado and Hernández (2008) reported that the adult stage lasted 15.56 days. In this research for the T2, the adult stage lasted 10 days, while in the T1 and T3 treatment it lasted 12 days, less than what they report in their work.
Romero Gutierrez and Cruz Reyes (2011) reported that the duration of the biological cycle, from egg to pupae, was 36.16 days, which was similar to the data obtained in the UNAN-León laboratory under controlled conditions and fed with an artificial soy-based diet. As can be seen, there is an average difference approximately for the T3 treatment of five more days, for the T1 treatment of 11 days and for the T2 treatment it was nine more days. According to Romero Gutierrez and Cruz Reyes (2011), this is due to the type of feeding and conditions in which these insects are raised, which is why the days of their biological cycle increase.
The treatment combinations were statistically validated. Based on the characterization of the periodical crossing of populations S. sunia, it is concluded that the best results are presented in treatments T1 and T3. The considerations of the study were that the biological cycle of the species S. sunia brought from the Field (T3) lasted 47 days, that of the Laboratory (T2) 45 days and that of the Crossing 41 days. The highest average larval weight of S. sunia obtained from T3 was 0.4288 mg. The best sex ratio of the species S. sunia was T3 (1.22:1). The longest treatment was T3 (30 mm). T1 obtained the highest number of eggs (1,744–5,670).
Based on these results, it is recommended to introduce genetic material every six months to maintain a good production of larvae of the species. It is also recommended to maintain stable climatic conditions (temperature and humidity) in the Insect Breeding Laboratory of the populations S. sunia (Montezano et al., 2014; Salinas-Sánchez et al., 2020). When preparing the diet, all the nutritional requirements must be met so that the reproduction of the S. sunia develops well. Finally, after moving to individual vessels, the diet is changed at least twice during the larval stage to prevent drying out and for better larval development.
Figshare: Data for: Cross-species characterization in the reproduction of S. sunia (Lepidoptera: Noctuidae). https://doi.org/10.6084/m9.figshare.21671669 (Real-Baca and Zuniga-Gonzalez, 2022b).
This project contains the following underlying data:
• Data.csv
• Fig 1.tif
• Fig 2.tif
• Fig 3.tif
• Table 1.csv
• Table 2.csv
• Table 3.csv
• Table 4.csv
• Table 5.csv
• Table 6.csv
• Table 7.csv
• Table 8.csv
Data are available under the terms of the Creative Commons Attribution 4.0 International license (CC-BY 4.0).
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Is the work clearly and accurately presented and does it cite the current literature?
Yes
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
Yes
If applicable, is the statistical analysis and its interpretation appropriate?
Yes
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Host plant resistance, Insect nutrition, Insect Immunity and Insecticide resistance
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Biological Control, Integrated pest management and Economic Entomology.
Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
No
If applicable, is the statistical analysis and its interpretation appropriate?
Partly
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Yes
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Biological control, entomology, micology
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Insect pest management
Is the work clearly and accurately presented and does it cite the current literature?
Yes
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
Yes
If applicable, is the statistical analysis and its interpretation appropriate?
Yes
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Yes
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Biological Control, Integrated pest management and Economic Entomology.
Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
Partly
If applicable, is the statistical analysis and its interpretation appropriate?
Yes
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Insect pest management
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