Next Article in Journal
The Adult, Larva, and Pupa of a New Pseudopyrochroa (Coleoptera: Pyrochroidae: Pyrochroinae) from China, with Molecular Phylogenetic Inferences
Next Article in Special Issue
Alientoma, a Dynamic Database for Alien Insects in Greece and Its Use by Citizen Scientists in Mapping Alien Species
Previous Article in Journal
Improving the Knowledge on Distribution, Food Preferences and DNA Barcoding of Natura 2000 Protected Species Paracossulus thrips (Lepidoptera, Cossidae) in Romania
Previous Article in Special Issue
Mealybug (Hemiptera: Pseudococcidae) Species Associated with Cacao Mild Mosaic Virus and Evidence of Virus Acquisition
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Immediate and Delayed Mortality of Four Stored-Product Pests on Concrete Surfaces Treated with Chlorantraniliprole

by
Nickolas G. Kavallieratos
1,*,
Maria C. Boukouvala
1,*,
Erifili P. Nika
1,
Nikoleta Eleftheriadou
2 and
Dimitrios N. Avtzis
2
1
Laboratory of Agricultural Zoology and Entomology, Department of Crop Science, Agricultural University of Athens, 75 Iera Odos Str., 11855 Athens, Attica, Greece
2
Forest Research Institute, Hellenic Agricultural Organization Demeter, 57006 Vassilika, Thessalonıki, Greece
*
Authors to whom correspondence should be addressed.
Insects 2021, 12(12), 1088; https://doi.org/10.3390/insects12121088
Submission received: 8 November 2021 / Revised: 29 November 2021 / Accepted: 1 December 2021 / Published: 4 December 2021

Abstract

:

Simple Summary

We examined the mortality caused by the anthranilic diamide, chlorantraniliprole, at four different doses applied on concrete (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2) in Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) adults and larvae, Rhyzopertha dominica (F.) (Coleoptera: Bostrychidae) adults, Sitophilus oryzae (L.) (Coleoptera: Curculionidae) adults, and Acarus siro L. (Sarcoptiformes: Acaridae) adults and nymphs. Mortality data were recorded after 1, 2, 3, 4, and 5 days to determine the immediate mortality. Furthermore, after the 5-day mortality counts, still living individuals were conveyed for 7 days to untreated concrete surfaces to estimate the delayed mortality. The highest immediate mortality was recorded for the larvae of T. castaneum, reaching 96.7%, followed by the adults of A. siro (92.2%) after 5 days of exposure to 0.5 mg a.i./cm2. Complete (100.0%) delayed mortality was noticed for T. castaneum (adults and larvae), S. oryzae, and A. siro (both as adults) at 0.5 mg a.i./cm2. Rhyzopertha dominica adults and A. siro nymphs exhibited 98.6% and 96.3% delayed mortality at the same dose, respectively. Overall, our results demonstrate that chlorantraniliprole is effective against all the species tested, causing varying immediate and delayed mortality rates at the developmental stages tested.

Abstract

Chlorantraniliprole is an effective pesticide against a plethora of pests, but its efficacy against stored-product pests is very poorly explored. In this study we treated concrete surfaces with four different doses of chlorantraniliprole (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2) against the red flour beetle, Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) adults and larvae, the lesser grain borer, Rhyzopertha dominica (F.) (Coleoptera: Bostrychidae) adults, the rice weevil, Sitophilus oryzae (L.) (Coleoptera: Curculionidae) adults, and the flour mite, Acarus siro L. (Sarcoptiformes: Acaridae) adults and nymphs, to examine the immediate mortalities after 1, 2, 3, 4, and 5 days of exposure. Additionally, the delayed mortality of the individuals that survived the 5-day exposure was also evaluated after a further 7 days on untreated concrete surfaces. We documented high mortality rates for all tested species and their developmental stages. After 5 days of exposure to 0.5 mg a.i./cm2, T. castaneum larvae and A. siro adults exhibited the highest immediate mortality levels, reaching 96.7% and 92.2%, respectively. Delayed mortality was also very high for all tested species and their developmental stages. Nymphs of A. siro displayed a 96.3% delayed mortality followed by the adults of R. dominica (98.6%) after exposure to 0.5 mg a.i./cm2. All other tested species and their developmental stages reached complete (100.0%) delayed mortality, where even 0.01 mg a.i./cm2 caused ≥86.6% delayed mortality in all species and their developmental stages. Taking into consideration the effectiveness of chlorantraniliprole on this wide range of noxious arthropods, coupled with its low toxicity towards beneficial arthropods and mammals, this pesticide could provide an effective management tool for stored-product pests in storage facilities.

1. Introduction

The red flour beetle, Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) is a serious insect pest of high economic importance, infesting several stored cereals and foodstuffs worldwide [1]. It is a secondary pest commonly found in mills, warehouses, grocery stores, bakeries, and pet stores [2,3,4,5]. The lesser grain borer, Rhyzopertha dominica (F.) (Coleoptera: Bostrychidae) seems to have been originally feeding on dried fruits and forest trees [6], and it is currently identified as one of the most destructive insect pests of stored products globally [2,6,7]. As a primary pest, its larvae and adults can attack the sound kernels in storage facilities, while it can occasionally infect ripe grains in the field [8]. The rice weevil, Sitophilus oryzae (L.) (Coleoptera: Curculionidae) is a major pest of stored products worldwide, capable of infesting a wide range of commodities such as wheat, maize, barley, sorghum, rye, oats, rice, millet, cottonseed, dallisgrass seed, vetch seed, beans, nuts, flour, pasta, and cassava [2,6,8]. As this species is an internal feeder and completes its entire development inside kernels [6], its larvae remain protected from contact insecticides applied on the external part of the grain [9]. The flour mite, Acarus siro L. (Sarcoptiformes: Acaridae) is the most significant mite, infesting mainly cereal products like flour and other commodities like cheese, hay, medicinal herbs, spices, baby food, and fishmeal [8,10,11,12]. It can be found worldwide in farms, warehouses, mills, and empty grain bins, tainting the products with a musty smell [8,12]. Based on the biological traits presented before, the successful management of these species is restrained by specific difficulties. For instance, several insecticides are not effective against R. dominica that has developed resistance to specific formulations (including phosphine) [7,13,14,15,16,17,18,19]. Similarly, S. oryzae has become resistant to many insecticides in different parts of the world [19,20], indicating that the management of this species in storage facilities requires special care. It is well documented that T. castaneum presents resistance to a wide spectrum of insecticides around the globe [20,21,22,23,24]. Finally, A. siro is resistant to numerous pesticides. For instance, etrimfos, pirimiphos-methyl, fenitrothion, and chlorpyrifos-methyl were not totally (100%) efficient against A. siro individuals throughout a 36-week-long trial [25], while, similarly, beta-cyfluthrin, deltamethrin, chlorpyrifos, and a mix of s-bioallethrin and deltamethrin did not result in killing A. siro individuals after 21 days of exposure [26]. Acarus siro can survive the exposure to diatomaceous earth (DE), such as 3 g/kg Dryacide, from a sample taken from the surface of the bins, for up to 40 weeks [27]. As it becomes evident, the need to examine and find new alternative insecticidal active ingredients against these stored-product pests is imperative.
Chlorantraniliprole is a novel insecticide that belongs to the chemical group of anthranilic diamides [28,29]. It has a unique mode of action, activating the ryanodine receptor in insects’ muscles and releasing the cellular calcium that causes the termination of feeding, increased lethargy, the paralysis of muscles, eventually leading to death [29,30,31,32]. In addition, chlorantraniliprole presents low mammalian toxicity and can kill a wide range of insect pests without harming beneficial arthropods [30,31,33,34]. For instance, it is very effective against species of agricultural importance belonging to different orders, e.g., Coleoptera, Lepidoptera, Hemiptera, Diptera, Isoptera, and Thysanoptera [35,36,37,38,39,40,41]. Furthermore, recent studies have verified the insecticidal activity of chlorantraniliprole applied on different commodities (i.e., barley, maize, oats, peeled rice, whole rice, and wheat) against the Mediterranean flour moth, Ephestia kuehniella Zeller (Lepidoptera: Pyralidae), the psocid, Liposcelis bostrychophila Badonnel (Psocoptera: Liposcelididae), R. dominica, S. oryzae, and the confused flour beetle, Tribolium confusum Jacquelin du Val (Coleoptera: Tenebrionidae) [42], or on maize against the larger grain borer, Prostephanus truncatus (Horn) (Coleoptera: Bostrychidae) [43]. However, there is limited knowledge about the efficacy of chlorantraniliprole applied on surfaces against stored-product pests. For example, this compound was examined as a surface treatment on concrete against the different life stages (i.e., eggs, young and old larvae, pupae and adults) of T. confusum [44]. Therefore, the objective of the present study is to simultaneously evaluate the immediate and delayed mortality of chlorantraniliprole applied on concrete surfaces against four important stored-product pests, i.e., T. castaneum adults and larvae, S. oryzae adults, R. dominica adults, and A. siro adults and nymphs.

2. Materials and Methods

2.1. Insect and Mite Species

The insect species used in the bioassays were obtained from colonies maintained under laboratory conditions since 2003. Tribolium castaneum was cultured on wheat flour containing 5% brewer’s yeast at 25 °C and at 65% relative humidity in continuous darkness [45]. Adults of this species were <2 weeks old and larvae were 3rd–4th instar [46]. Rhyzopertha dominica and S. oryzae were reared on whole wheat at 25 °C at 65% relative humidity, and <2-week-old adults of these species were examined [47]. The initial population of A. siro was collected from wheat in Greek storage facilities in 2004, and since then it has been reared under laboratory conditions. The A. siro rearing medium consisted of a mixture of oat flakes, wheat germ, and the extract of dried yeast at a 10:10:1 w/w ratio. The colonies were kept at 25 °C and at 80% relative humidity. For the tests, the nymphs and adults of A. siro were selected according to their external morphology, i.e., the bodies of adults are larger and bear longer hairs than the bodies of nymphs [48]. All the above species were reared in continuous darkness.

2.2. Insecticidal Formulation

The formulation of chlorantraniliprole, Coragen® SC (suspension concentrate) with a 200 g/L active ingredient a.i., which was provided by Dupont (Halandri, Greece), was used in the experiments.

2.3. Bioassays

Chlorantraniliprole was examined at four doses: 0.01, 0.05, 0.1, and 0.5 mg a.i./cm2. The experiments were carried out in a completely randomized block design, with three replicates and three subreplicates. Petri dishes that were 8 cm in diameter and 1.5 cm high, with a surface area of 50.27 cm2 each, were used. The concrete surface was made one day before the beginning of the tests by filling the bottoms of the Petri dishes with the CEM I 52.5 N material (Durostick, Aspropyrgos, Greece). To prevent the escape of the exposed individuals, the upper internal walls of all dishes were covered with polytetrafluoroethylene (60 wt% dispersion in water) (Sigma-Aldrich Chemie GmbH, Taufkirchen, Germany).
Spraying was conducted with the use of an AG-4 airbrush (Mecafer S.A., Valence, France), where 1 mL of an aqueous solution that contained the appropriate volume of the formulation corresponding to each dose was applied on concrete surface as a fine mist. The airbrush was cleaned with acetone after the spraying of each dose. A quantity of 0.5 g clean and pesticide-free whole wheat kernels without infestation was placed on each concrete surface after spraying, as food, for R. dominica, S. oryzae, and A. siro. For T. castaneum, the same quantity of soft white wheat flour (a variety mixture made from the endosperm only) was used in the experiments. An additional series of dishes were prepared and sprayed with distilled water (1 mL per dish) with a different AG-4 airbrush, as described above, to serve as controls. Subsequently, 10 individuals were transferred into each dish, and all dishes were put inside incubators set at 25 °C and at 65% relative humidity in continuous darkness. Mortality was determined under an Olympus stereomicroscope (Olympus SZX9, Bacacos S.A., Athens, Greece) after 1, 2, 3, 4, and 5 days of exposure in the treated dishes. After the 5th day of exposure, surviving individuals of each treated or untreated dish were transferred to new unsprayed concrete surfaces that also contained the same quantity of food for each species. The dishes were transferred again into the incubators with the same conditions for an additional period of 7 days. After this interval, the new dishes were opened and the number of the dead individuals per dish was counted, as described above.

2.4. Data Analysis

For all tested species, the immediate or delayed mortality of the controls was low (<5%), so no correction was considered necessary. The repeated measures model was used to separately analyze data for the immediate mortality of each tested species and developmental stage [49]. The repeated factor was the exposure interval, while mortality was the response variable. The dose was the main effect. Data for delayed mortality were submitted to a two-way ANOVA, with the species/developmental stage and dose as the main effects. The associated interaction of the main effects was also considered in the analysis. Prior to the analysis, the transformation of data to a log (x + 1) scale was carried out in order to normalize the variance [50,51]. Means were separated by the Tukey–Kramer honest significant difference (HSD) test at the 0.05 significance level [52]. All analyses were conducted using the JMP 14 software [53].

3. Results

3.1. Immediate Mortality

Between and within the exposure intervals, all main effects were significant for all tested species and life stages, except for R. dominica adults (Table 1).
The mortality of T. castaneum adults was very low after 3 days of exposure in all tested doses and did not exceed 35.6% at 0.5 mg a.i./cm2 (Table 2). Mortality increased further, reaching 56.7% at 0.5 mg a.i./cm2, while at the other doses it ranged between 30.0% and 44.4% after 4 days of exposure. One day later, chlorantraniliprole killed 81.1% of the exposed adults at the highest dose (0.5 mg a.i./cm2) while it caused moderate mortality at the lower doses (i.e., 0.01, 0.05, and 0.1 mg a.i./cm2), ranging from 42.2% to 61.1%.
After 2 days of exposure, the mortality of T. castaneum larvae remained at low levels, reaching 33.3% mortality (Table 3). One day later, mortality increased further, ranging between 21.1% and 37.8% at 0.01, 0.05, and 0.1 mg a.i./cm2, and 60.0% at 0.5 mg a.i./cm2. After 4 days of exposure, mortality reached 77.8% at 0.5 mg a.i./cm2, while at 0.05 and 0.1 mg a.i./cm2, it was moderate (48.9% and 58.9%, respectively). After 5 days of exposure, chlorantraniliprole killed almost all larvae (96.7%) at 0.5 mg a.i./cm2.
Regarding the immediate mortality of S. oryzae, after 3 days of exposure, it was very low at all tested doses and did not exceed 23.3% at 0.5 mg a.i./cm2 (Table 4). The overall mortality did not exceed 45.6% after 4 days of exposure. At 5 days post-exposure, 80.0% of the exposed adults died on concrete treated with 0.5 mg a.i./cm2, while mortality rates at all the other doses ranged between 45.6% and 71.1%.
After 4 days of exposure, the percentages of dead R. dominica adults was low for all tested doses, reaching 32.2% at 0.5 mg a.i./cm2 (Table 5). One day later, mortality increased without significant differences among doses, ranging from 34.4% to 50.0%.
The mortality levels of A. siro adults was very low at doses ≤0.1 mg a.i./cm2, reaching 38.9%, while at 0.5 mg a.i./cm2, moderate mortality was noted (54.4%) 3 days post-exposure (Table 6). One day later, mortality at 0.01 mg a.i./cm2 remained at low levels (38.9%), but at doses ≥0.1 mg a.i./cm2, it ranged between 50.0% and 72.2%. After 5 days of exposure, chlorantraniliprole killed 92.2% of the exposed adults at the highest dose, while at 0.01 mg a.i./cm2, moderate mortality was recorded (65.6%).
Regarding A. siro nymphs, after 3 days of exposure, mortality was low at all tested doses, reaching 46.7% at 0.5 mg a.i./cm2 (Table 7). Nymphal mortality ranged between 37.8% and 61.1% at 4 days post-exposure. Moderate mortality was recorded at doses ≥0.05 mg a.i./cm2, reaching 73.3% at 0.5 mg a.i./cm2 after 5 days of exposure.

3.2. Delayed Mortality of the Tested Species

The main effect dose was significant for all species (Table 8). Delayed mortality was high for T. castaneum adults, given that >91.0% of the adults died on concrete treated with 0.01, 0.05, or 0.1 mg a.i./cm2, while 100.0% was recorded at 0.5 mg a.i./cm2 (Table 9). The same trend was noted for larval delayed mortality of this species. Complete mortality was noticed at 0.5 mg a.i./cm2. Moreover, 100.0% delayed mortality was noted for S. oryzae adults at 0.1 and 0.5 mg a.i./cm2. Rhyzopertha dominica adults reached 96.7% and 98.6% delayed mortality at 0.1 and 0.5 mg a.i./cm2, respectively. Concerning A. siro, adults were more susceptible than nymphs. All adults died at 0.1 and 0.5 mg a.i./cm2. However, 94.4% and 96.3% of the exposed nymphs died on concrete treated with 0.1 and 0.5 mg a.i./cm2, respectively.

4. Discussion

Our results indicate that chlorantraniliprole is a promising pesticide for the effective control of the adults and larvae of T. castaneum, the adults of S. oryzae and R. dominica, and the adults and nymphs of A. siro, when applied on concrete surfaces. In the present study, chlorantraniliprole killed 81.1% of T. castaneum adults, 96.7% of T. castaneum larvae, 80.0% of S. oryzae adults, 50.0% of R. dominica, 92.2% of A. siro adults, and 73.3% of A. siro nymphs after 5 days of exposure to 0.5 a.i./cm2. In a former study, Kavallieratos et al. [42] investigated the efficacy of two chlorantraniliprole formulations (WG and SC) as grain protectants against L. bostrychophila, R. dominica, S. oryzae adults, E. kuehniella larvae, and T. confusum adults and larvae. The 10 mg a.i./kg of grain of the WG formulation killed 95.6% of S. oryzae adults after 7 days of exposure on treated whole rice, while at the same dose, the SC formulation caused the mortality of 99.4% exposed individuals. Both chlorantraniliprole formulations killed 100.0% of S. oryzae adults after 14 days of exposure to the 10 mg a.i./kg of grain. Concerning R. dominica, the WG formulation at 10 mg a.i./kg of grain killed 88.3% of the adults after 7 days of exposure and 100.0% after 14 days of exposure on whole rice and wheat, respectively. The SC chlorantraniliprole was also effective at causing 83.3% and 96.7% mortality rates 7 and 14 days post-exposure, respectively, to treated whole rice. Furthermore, both chlorantraniliprole formulations effectively controlled E. kuehniella larvae, L. bostrychophila adults, and T. confusum adults and larvae on several commodities (e.g., hard wheat, barley, maize, peeled rice, whole rice, and oats). Similarly, Saglam et al. [44] documented that 0.1 mg a.i./cm2 sprayed on concrete killed 66%, 100.0%, and 64% of T. confusum adults, young larvae, and old larvae, respectively. It also delayed the adult emergence on the first 5 days of the experiment. Chlorantraniliprole (WG and SC) is also effective as maize protectant against P. truncatus. In a recent study, Boukouvala and Kavallieratos [43] found that 10 mg a.i. WG/kg of grain and 10 mg a.i. SC/kg of grain killed 98.9% and 96.1% of the exposed individuals after 14 days of exposure, respectively, at 30 °C. Although chlorantraniliprole is not yet authorized for the management of stored-product pests, the aforementioned findings are valuable inputs for its potential use. These research efforts are of particular importance as the number of registered plant protection products in stored-product protection is considerably reduced [54]. Therefore, chlorantraniliprole can be clasified as an a.i. that could potentially recieve registration to be used in storage facilities as a grain protectant and/or as a structural treatment.
Surface treatments constitute an effective approach for the management of stored-product pests. To date, a plethora of pesticides have been applied onto several types of surfaces under different scenarios. For instance, when Kavallieratos et al. [55] treated polypropylene storage bags with alpha-cypermethrin, the immediate mortality of R. dominica and S. oryzae adults was 37.8% and 40.0% at 5 days post-exposure, respectively. Adults of T. castaneum that were exposed to plywood, tiles, and concrete treated with chlorfenapyr exhibited different levels of survival (40.0%, 25.5%, and 2.5%, respectively), concluding that the type of the treated surface affects the efficacy of the tested formulation [56]. Similarly, Vassilakos et al. [57] evaluated ceramic tiles, plywood, concrete, and galvanized steel treated with spinetoram against T. confusum, S. oryzae, S. granarius, R. dominica, the rusty grain beetle, Cryptolestes ferrugineus (Stephens) (Coleoptera: Laemophloeidae), and Oryzaephilus surinamensis (L.) (Coleoptera: Silvanidae) adults. The different treated surfaces led to different mortality rates among all the exposed pests. For example, 0.05 mg spinetoram/cm2 killed 77.4%, 68.1%, 89.0%, and 59.2% of T. confusum adults on ceramic tiles, plywood, concrete, and galvanized steel, respectively, at 7 days post-exposure. Furthermore, the mortality of E. kuehniella larvae caused by thiamethoxam, alpha-cypermethrin, and deltamethrin treated on woven polypropylene (0.10 mg a.i./cm2) ranged between 40.0% and 82.2% [58]. Our findings document that chlorantraniliprole caused even higher mortality rates than the aforementioned formulations in some of the stored-product pests, as in the cases of T. castaneum larvae and A. siro adults. The fact that chlorantraniliprole killed almost all young larvae of T. castaneum under the short exposure scenario followed in our study is of particular importance. This is because chlorantraniliprole can cause the rapid collapse of the larval population upon contact to treated concrete and can consequently prohibit the emergence of adults which, as flyers and walkers, easily colonize stored food commodities [8,59,60]. Whether chlorantraniliprole can perform similarly to the older larvae of T. castaneum merits further investigation. In an earlier study, Saglam et al. [44] showed that when the old larvae of T. confusum came into contact with concrete surfaces treated with chlorantraniliprole, they exhibited tolerance to this toxicant, taking into account that around 50% of larvae survived after 14 days of exposure. Our study provides new information about the management of A. siro on surface treatment, given that there is limited knowledge, mostly coming from previous decades. For example, the DEs SilicoSec and Diasecticide killed 28–98% and 64–88% of A. siro adults after 24 h of exposure to three slurry doses (2.5, 5, and 10 g/m2) [61]. Although we obtained low mortality rates after 24 h of exposure with A. siro adults, 92.2% finally died 5 days post-exposure, which is also considered a short exposure interval.
In our study, the delayed mortality was extremely high, ranging between 96.3% and 100.0% in all tested species and their developmental stages. This is an important finding as it provides a plausible scenario of the arthropods moving from treated to untreated areas that may lead to their colonization by the pests [55,62,63,64]. This highly toxic effect of delayed mortality is also evident in the cases of several other pesticides. For instance, alpha-cypermethrin caused moderate-to-high delayed mortality in R. dominica (from 37.8% to 46.7%) and S. oryzae adults (from 32.2% to 60.0%) [55]. Chlorfenapyr killed 56.7% of S. oryzae adults after being transferred onto untreated surfaces (polypropylene bags) [55]. As with immediate mortality, delayed mortality may differ depending on the surface that the pesticide is applied. For example, 0.1 mg spinetoram/cm2 killed 100.0% of R. dominica on concrete, but 97.0% on galvanised steel [57]. The presence of untreated food lowered the delayed mortality rates of S. oryzae adults from 100.0% to 98.8% and from 91.4% to 78.7% with the T. confusum adults [57]. In addition to the aforementioned parameters that affect the rates of delayed mortality, the species and the developmental stage of the exposed pest are equally important, something that was clearly demonstrated both in the current study and in previous investigations. For example, thiamethoxan killed 3.3% of T. molitor adults and 35.6% of T. molitor large larvae, while the same pesticide killed 63.3% of T. granarium adults and 1.1% of T. granarium old larvae [62].

5. Conclusions

In conclusion, our study provides new data towards the efficacy of chlorantraniliprole on concrete at four doses against important arthropod pests of stored products. On the basis of our findings, chlorantraniliprole can be a useful management tool since it caused high levels of both immediate and delayed mortality to the majority of the tested species and their developmental stages. However, further experimentation is required to assess the efficacy of chlorantraniliprole applied on other types of surfaces (e.g., storage bags) under different environmental conditions (temperature and relative humidity), doses, exposure intervals, and other stored-product pests in conjunction with their egg laying capacities.

Author Contributions

Designed research, N.G.K.; methodology, N.G.K., M.C.B. and E.P.N.; investigation, N.G.K., M.C.B., E.P.N., N.E. and D.N.A.; data curation, N.G.K., M.C.B. and E.P.N. formal analysis, M.C.B. and N.G.K.; writing—original draft, N.G.K., M.C.B. and E.P.N.; writing—review and editing, N.G.K., M.C.B., E.P.N., N.E. and D.N.A.; supervision, N.G.K.; resources, N.G.K.; funding acquisition, N.G.K. All authors have read and agreed to the published version of the manuscript.

Funding

The research was partially funded by the 34.0889 project (Special Account for Research Funds of the Agricultural University of Athens).

Institutional Review Board Statement

Not applicable.

Data Availability Statement

Data are contained within the article.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Ridley, A.W.; Hereward, J.P.; Daglish, G.J.; Raghu, S.; Collins, P.J.; Walter, G.H. The spatiotemporal dynamics of Tribolium castaneum (Herbst): Adult flight and gene flow. Mol. Ecol. 2011, 20, 1635–1646. [Google Scholar] [CrossRef]
  2. Aitken, A.D. Insect Travelers, I: Coleoptera. Technical Bulletin 31; H.M.S.O.: London, UK, 1975. [Google Scholar]
  3. Hagstrum, D.W.; Subramanyam, B. Stored-Product Insect Resource; AACC International: St. Paul, MN, USA, 2009. [Google Scholar]
  4. Mahroof, R.M.; Hagstrum, D.W. Biology, behavior, and ecology of insects in processed commodities. In Stored Product Protection; Hagstrum, D.W., Phillips, T.W., Cuperus, G., Eds.; Kansas State University: Manhattan, KS, USA, 2012; pp. 33–44. [Google Scholar]
  5. Kumar, R. Insect Pests on Stored Grain. Biology, Behavior, and Management Strategies; Apple Academic Press: Waretown, NJ, USA, 2017. [Google Scholar]
  6. Mason, L.J.; McDonough, M. Biology, behavior, and ecology of stored grain and legume insects. In Stored Product Protection; Hagstrum, D.W., Phillips, T.W., Cuperus, G., Eds.; Kansas State University: Manhattan, KS, USA, 2012; pp. 7–20. [Google Scholar]
  7. Edde, P.A. A review of the biology and control of Rhyzopertha dominica (F.) the lesser grain borer. J. Stored Prod. Res. 2012, 48, 1–18. [Google Scholar] [CrossRef]
  8. Hill, D.S. Pests of Stored Foodstuffs and Their Control; Kluwer Academic Publishers: New York, NY, USA, 2003. [Google Scholar]
  9. Arthur, F.H.; Throne, J.E. Efficacy of diatomaceous earth to control internal infestations of rice weevil and maize weevil (Coleoptera: Curculionidae). J. Econ. Entomol. 2003, 96, 510–518. [Google Scholar] [CrossRef]
  10. Mullen, G.R.; OConnor, B.M. Mites (Acari). In Medical and Veterinary Entomology; Mullen, G.R., Durden, L.A., Eds.; Academic Press: London, UK, 2002; pp. 449–516. [Google Scholar]
  11. Robinson, W.H. Urban Insects and Arachnids; Cambridge University Press: Cambridge, UK, 2005. [Google Scholar]
  12. Hagstrum, D.W.; Klejdysz, T.; Subramanyam, B.; Nawrot, J. Atlas of Stored-Product Insects and Mites; AACC International: St. Paul, MN, USA, 2013. [Google Scholar]
  13. Guedes, R.N.C.; Dover, B.A.; Kambhampati, S. Resistance to chlorpyrifosmethyl, pirimiphos-methyl, and malathion in Brazilian and U.S. populations of Rhyzopertha dominica (Coleoptera: Bostrichidae). J. Econ. Entomol. 1996, 89, 27–32. [Google Scholar] [CrossRef]
  14. Lorini, I.; Galley, D.J. Deltamethrin resistance in Rhyzopertha dominica (F.) (Coleoptera: Bostrichidae), a pest of stored grain in Brazil. J. Stored Prod. Res. 1999, 35, 37–45. [Google Scholar] [CrossRef]
  15. Collins, P.J.; Daglish, G.J.; Bengston, M.; Lambkin, T.M.; Pavic, H. Genetics of resistance to phosphine in Rhyzopertha dominica (Coleoptera: Bostrichidae). J. Econ. Entomol. 2002, 95, 862–869. [Google Scholar] [CrossRef] [PubMed]
  16. Daglish, G.J. Impact of resistance on the efficacy of binary combinations of spinosad, chlorpyriphos-methyl and s-methoprene against five stored-grain beetles. J. Stored Prod. Res. 2008, 44, 71–76. [Google Scholar] [CrossRef]
  17. Schlipalius, D.; Chen, W.; Collins, P.; Nguyen, T.; Reilly, P.; Ebert, P. Gene interactions constrain the course of evolution of phosphine resistance in the lesser grain borer, Rhyzopertha dominica. Heredity 2008, 100, 506–516. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  18. Athanassiou, C.G.; Arthur, F.H.; Kavallieratos, N.G.; Throne, J.E. Efficacy of spinosad and methoprene, applied alone or in combination, against six stored product insect species. J. Pest. Sci. 2011, 84, 61–67. [Google Scholar] [CrossRef]
  19. Wakil, W.; Kavallieratos, N.G.; Usman, M.; Gulzar, S.; El-Shafie, H.A.F. Detection of phosphine resistance in field populations of four key stored-grain insect pests in Pakistan. Insects 2021, 12, 288. [Google Scholar] [CrossRef] [PubMed]
  20. Attia, M.A.; Wahba, T.F.; Shaarawy, N.; Moustafa, F.I.; Guedes, R.N.C.; Dewer, Y. Stored grain pest prevalence and insecticide resistance in Egyptian populations of the red flour beetle Tribolium castaneum (Herbst) and the rice weevil Sitophilus oryzae (L.). J. Stored Prod. Res. 2020, 87, 101611. [Google Scholar] [CrossRef]
  21. Halliday, W.R.; Arthur, E.H.; Zettler, J.L. Resistance status of red flour beetle (Coleoptera: Tenebrionidae) infesting stored peanuts in the southeastern United States. J. Econ. Entomol. 1988, 76, 717–722. [Google Scholar] [CrossRef]
  22. Arthur, F.H. Grain protectants: Current status and prospects for the future. J. Stored Prod. Res. 1996, 32, 239–302. [Google Scholar] [CrossRef]
  23. Stadler, T.; Subramanyam, B.; Ferrero, A.A. Monitoring for insecticide resistance in major stored product pests in Argentina: A review. Agriscientia 2003, 20, 99–110. [Google Scholar]
  24. Rossi, E.; Cosimi, S.; Loni, A. Insecticide resistance in Italian populations of Tribolium flour beetles. Bull. Insectol. 2010, 63, 251–258. [Google Scholar]
  25. Thomas, K.P.; Pinniger, D.B.; Wilkin, D.R. An assessment of chlorpyrifos-methyl, etrimfos, fenitrothion and pirimiphos-methyl as grain protectants. Pestic. Sci. 1987, 21, 57–72. [Google Scholar] [CrossRef]
  26. Hubert, J.; Stejskal, V.; Munzbergova, Z.; Hajslova, J.; Arthur, F.H. Toxicity and efficacy of selected pesticides and new acaricides to stored product mites (Acari: Acaridida). Exp. Appl. Acarol. 2007, 42, 283–290. [Google Scholar] [CrossRef] [PubMed]
  27. Cook, D.A.; Armitage, D.M. Efficacy of a diatomaceous earth against mite and insect populations in small bins of wheat under conditions of low temperature and high humidity. Pest Manag. Sci. 2000, 56, 591–596. [Google Scholar] [CrossRef]
  28. Lahm, G.P.; Selby, T.P.; Freudenberger, J.H.; Stevenson, T.M.; Myers, B.J.; Seburyamo, G.; Smith, B.K.; Flexner, L.; Clark, C.E.; Cordova, D. Insecticidal anthranilic diamides: A new class of potent ryanodine receptor activators. Bioorg. Med. Chem. Lett. 2005, 15, 4898–4906. [Google Scholar] [CrossRef]
  29. Cordova, D.; Benner, E.; Sacher, M.; Rauh, J.; Sopa, J.; Lahm, G.; Selby, T.; Stevenson, T.; Flexner, L.; Gutteridge, S.; et al. Anthranilic diamides: A new class of insecticides with a novel mode of action, ryanodine receptor activation. Pestic. Biochem. Physiol. 2006, 84, 196–214. [Google Scholar] [CrossRef]
  30. Lahm, G.P.; Stevenson, T.M.; Selby, T.P.; Freudenberger, J.H.; Cordova, D.; Flexner, L.; Bellin, C.A.; Dubas, C.M.; Smith, B.K.; Hughes, K.A.; et al. RynaxypyrTM: A new insecticidal anthranilic diamide that acts as a potent and selective receptor activator. Bioorg. Med. Chem. Lett. 2007, 17, 6274–6279. [Google Scholar] [CrossRef]
  31. Lahm, G.P.; Cordova, D.; Barry, J.D. New and selective ryanodine receptor activators for insect control. Bioorg. Med. Chem. 2009, 17, 4127–4133. [Google Scholar] [CrossRef]
  32. Sattelle, D.B.; Cordova, D.; Cheek, T.R. Insect ryanodine receptors: Molecular targets for novel pest control chemicals. Invertebr. Neurosci. 2008, 8, 107–119. [Google Scholar] [CrossRef] [PubMed]
  33. Liu, F.; Zhang, X.; Gui, Q.Q.; Xu, Q.J. Sublethal effects of four insecticides on Anagrus nilaparvatae (Hymenoptera: Mymaridae), an important egg parasitoid of the rice planthopper Nilaparvata lugens (Homoptera: Delphacidae). Crop Prot. 2012, 37, 13–19. [Google Scholar] [CrossRef]
  34. Nawaz, M.; Cai, W.; Jing, Z.; Zhou, X.; Mabubu, J.I.; Hua, H. Toxicity and sublethal effects of chlorantraniliprole on the development and fecundity of a non-specific predator, the multicolored Asian lady beetle, Harmonia axyridis (Pallas). Chemosphere 2017, 178, 496–503. [Google Scholar] [CrossRef] [PubMed]
  35. Hummel, N.A.; Mészáros, A.; Ring, D.R.; Beuzelin, J.M.; Stout, M.J. Evaluation of seed treatment insecticides for management of the rice water weevil, Lissorhoptrus oryzophilus Kuschel (Coleoptera: Curculionidae), in commercial rice fields in Louisiana. Crop Prot. 2014, 65, 37–42. [Google Scholar] [CrossRef]
  36. Plata Rueda, A.; Martínez, L.C.; Costa, N.C.R.; Zanuncio, J.C.; Fernandes, M.E.D.S.; Serrão, J.E.; Guedes, R.N.C.; Fernandes, F.L. Chlorantraniliprole–mediated effects on survival, walking abilities, and respiration in the coffee berry borer, Hypothenemus hampei. Ecotoxicol. Environ. Saf. 2019, 172, 53–58. [Google Scholar] [CrossRef]
  37. Teixeira, L.A.F.; Gut, L.J.; Wise, J.C.; Isaacs, R. Lethal and sublethal effects of chlorantraniliprole on three species of Rhagoletis fruit flies (Diptera: Tephritidae). Pest Manag. Sci. 2008, 65, 137–143. [Google Scholar] [CrossRef]
  38. Liu, J.L.; Yang, X.; Chen, X.; Wu, J.C. Suppression of fecundity, Nlvg gene expression and vitellin content in Nilaparvata lugens Stål (Hemiptera: Delphacidae) adult females exposed to indoxacarb and chlorantraniliprole. Pestic. Biochem. Physiol. 2012, 104, 206–211. [Google Scholar] [CrossRef]
  39. Neoh, K.B.; Hu, J.; Yeoh, B.H.; Lee, C.Y. Toxicity and horizontal transfer of chlorantraniliprole against the Asian subterranean termite Coptotermes gestroi (Wasmann): Effects of donor: Recipient ratio, exposure duration and soil type. Pest Manag. Sci. 2012, 68, 749–756. [Google Scholar] [CrossRef]
  40. He, F.; Sun, S.; Tan, H.; Sun, X.; Qin, C.; Ji, S.; Li, X.; Zhang, J.; Jiang, X. Chlorantraniliprole against the black cutworm Agrotis ipsilon (Lepidoptera: Noctuidae): From biochemical/physiological to demographic responses. Sci. Rep. 2019, 9, 1–17. [Google Scholar]
  41. Dale, A.G.; Borden, M.A. Evaluation of reduced-risk insecticides to control chilli thrips (Thysanoptera: Thripidae) and conserve natural enemies on ornamental plants. Fla. Entomol. 2018, 101, 237–243. [Google Scholar] [CrossRef] [Green Version]
  42. Kavallieratos, N.G.; Athanassiou, C.G.; Boukouvala, M.C. Insecticidal effect of chlorantraniliprole against major stored-product insect pests in different grain commodities under laboratory tests. Pest Manag. Sci. 2013, 69, 1141–1154. [Google Scholar] [CrossRef] [PubMed]
  43. Boukouvala, M.C.; Kavallieratos, N.G. Evaluation of two formulations of chlorantraniliprole as maize protectants for the management of Prostephanus truncatus (Horn) (Coleoptera: Bostrychidae). Insects 2021, 12, 194. [Google Scholar] [CrossRef]
  44. Saglam, O.; Athanassiou, C.G.; Vassilakos, T.N. Comparison of spinetoram, imidacloprid, thiamethoxam and chlorantraniliprole against life stages of Tribolium confusum Jacquelin du Val (Coleoptera: Tenebrionidae) on concrete. Crop Prot. 2013, 53, 85–95. [Google Scholar] [CrossRef]
  45. Athanassiou, C.G.; Kavallieratos, N.G.; Chiriloaie, A.; Vassilakos, T.N.; Fătu, V.; Drosu, S.; Ciobanu, M.; Dudoiu, R. Insecticidal efficacy of natural diatomaceous earth deposits from Greece and Romania against four stored grain beetles: The effect of temperature and relative humidity. Bull. Insectol. 2016, 69, 25–34. [Google Scholar]
  46. Kavallieratos, N.G.; Nika, E.P.; Skourti, A.; Ntalli, N.; Boukouvala, M.C.; Ntalaka, C.T.; Maggi, F.; Rakotosaona, R.; Cespi, M.; Perinelli, D.R.; et al. Developing a Hazomalania voyronii essential oil nanoemulsion for the eco-friendly management of Tribolium confusum, Tribolium castaneum and Tenebrio molitor larvae and adults on stored wheat. Molecules 2021, 26, 1812. [Google Scholar] [CrossRef]
  47. Kavallieratos, N.G.; Athanassiou, C.G.; Arthur, F.H. Effectiveness of insecticide-incorporated bags to control stored-product beetles. J. Stored Prod. Res. 2017, 70, 18–24. [Google Scholar] [CrossRef] [Green Version]
  48. Hughes, A.M. The Mites of Stored Food and Houses. Technical Bulletin 9; H.M.S.O.: London., UK, 1976. [Google Scholar]
  49. Sall, J.; Lehman, A.; Creighton, L. JMP start statistics. In A Guide to Statistics and Data Analysis Using JMP and JMP in Software; Duxbury Press: Belmont, ON, Canada, 2001. [Google Scholar]
  50. Zar, J.H. Biostatistical Analysis; Pearson Education Limited: Essex, UK, 2014. [Google Scholar]
  51. Scheff, D.S.; Arthur, F.H. Fecundity of Tribolium castaneum and Tribolium confusum adults after exposure to deltamethrin packaging. J. Pest Sci. 2018, 91, 717–725. [Google Scholar] [CrossRef]
  52. Sokal, R.R.; Rohlf, F.J. Biometry; Freeman & Company: New York, NY, USA, 1995. [Google Scholar]
  53. SAS Institute Inc. Using JMP 14; SAS Institute Inc.: Cary, NC, USA, 2018. [Google Scholar]
  54. Arthur, F.H. Efficacy of combinations of methoprene and deltamethrin as long-term commodity protectants. Insects 2019, 10, 50. [Google Scholar] [CrossRef] [Green Version]
  55. Kavallieratos, N.G.; Athanassiou, C.G.; Nika, E.P.; Boukouvala, M.C. Efficacy of alpha-cypermethrin, chlorfenapyr and pirimiphos-methyl applied on polypropylene bags for the control of Prostephanus truncatus (Horn), Rhyzopertha dominica (F.) and Sitophilus oryzae (L.). J. Stored Prod. Res. 2017, 73, 54–61. [Google Scholar] [CrossRef]
  56. Arthur, F.H. Efficacy of chlorfenapyr against Tribolium castaneum and Tribolium confusum (Coleoptera: Tenebrionidae) adults exposed on concrete, vinyl tile, and plywood surfaces. J. Stored Prod. Res. 2008, 44, 145–151. [Google Scholar] [CrossRef]
  57. Vassilakos, T.N.; Athanassiou, C.G.; Chloridis, A.S.; Dripps, J.E. Efficacy of spinetoram as a contact insecticide on different surfaces against stored-product beetle species. J. Pest Sci. 2014, 87, 485–494. [Google Scholar] [CrossRef]
  58. Papanikolaou, N.E.; Kavallieratos, N.G.; Boukouvala, M.C.; Malesios, C. (Quasi)-binomial vs. Gaussian models to evaluate thiamethoxam, pirimiphos-methyl, alpha- cypermethrin and deltamethrin on different types of storage bag materials against Ephestia kuehniella Zeller (Lepidoptera: Pyralidae) and Tribolium confusum Jacquelin du Val (Coleoptera: Tenebrionidae). Insects 2021, 12, 182. [Google Scholar] [PubMed]
  59. Perez Mendoza, J.; Campbell, J.F.; Throne, J.E. Effects of rearing density, age, sex, and food deprivation on flight initiation of the red flour beetle (Coleoptera: Tenebrionidae). J. Econ. Entomol. 2011, 104, 443–451. [Google Scholar] [CrossRef] [Green Version]
  60. Perez Mendoza, J.; Campbell, J.F.; Throne, J.E. Influence of age, mating status, sex, quantity of food, and long-term food deprivation on red flour beetle (Coleoptera: Tenebrionidae) flight initiation. J. Econ. Entomol. 2011, 104, 2078–2086. [Google Scholar] [CrossRef] [PubMed]
  61. Collins, D.A.; Cook, D.A. Laboratory studies evaluating the efficacy of diatomaceous earths, on treated surfaces, against stored-product insect and mite pests. J. Stored Prod. Res. 2006, 42, 51–60. [Google Scholar] [CrossRef]
  62. Athanassiou, C.G.; Kavallieratos, N.G.; Boukouvala, M.C.; Mavroforos, M.E.; Kontodimas, D.C. Efficacy of alpha-cypermethrin and thiamathoxam against Trogoderma granarium Everts (Coleoptera: Dermestidae) and Tenebrio molitor L. (Coleoptera: Tenebrionidae) on concrete. J. Stored Prod. Res. 2015, 62, 101–107. [Google Scholar] [CrossRef]
  63. Ghimire, M.N.; Myers, S.W.; Arthur, F.H.; Phillips, T.W. Susceptibility of Trogoderma granarium Everts and Trogoderma inclusum LeConte (Coleoptera: Dermestidae) to residual contact insecticides. J. Stored Prod. Res. 2017, 72, 75–82. [Google Scholar] [CrossRef] [Green Version]
  64. Skourti, A.; Kavallieratos, N.G.; Papanikolaou, N.E. How is fitness of Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) affected when different developmental stages are exposed to chlorfenapyr? Insects 2020, 11, 542. [Google Scholar] [CrossRef] [PubMed]
Table 1. MANOVA parameters for main effects and associated interaction for mortality of Tribolim castaneum adults and larvae, Sitophilus oryzae adults, Rhyzopertha dominica adults, and Acarus siro adults and nymphs between and within exposure intervals (error DF = 32).
Table 1. MANOVA parameters for main effects and associated interaction for mortality of Tribolim castaneum adults and larvae, Sitophilus oryzae adults, Rhyzopertha dominica adults, and Acarus siro adults and nymphs between and within exposure intervals (error DF = 32).
EffectDFT. castaneumT. castaneumS. oryzaeR. dominicaA. siroA. siro
AdultsLarvaeAdultsAdultsAdultsNymphs
Between exposure intervals
 Source FpFpFpFpFpFp
 Intercept14928<0.011293.2<0.012189.7<0.01447.9<0.011587.6<0.015554.6<0.01
 Dose236.7<0.019.00.018.80.013.60.0210.7<0.0119.4<0.01
Within exposure intervals
 Source FpFpFpFpFpFp
 Exposure46285.2<0.01112.6<0.016638.0<0.01101.9<0.0183.2<0.0168.2<0.01
 Exposure × dose89.1<0.012.40.015.8<0.010.70.753.10.012.70.01
Table 2. Mean immediate mortality (% ± SE) of Tribolium castaneum adults exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded. Where dashes exist, no analysis was performed.
Table 2. Mean immediate mortality (% ± SE) of Tribolium castaneum adults exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded. Where dashes exist, no analysis was performed.
Exposure1 Day2 Days3 Days4 Days5 DaysFp
Dose (mg a.i./cm2)
0.010.0 ± 0.0 D0.0 ± 0.0 Db12.2 ± 1.5 Cc30.0 ± 1.7 Bc42.2 ± 2.8 Ac1045.9<0.01
0.050.0 ± 0.0 D0.0 ± 0.0 Db18.9 ± 2.0 Cb36.7 ± 3.3 Bbc54.4 ± 2.9 Ab790.0<0.01
0.10.0 ± 0.0 C2.2 ± 1.5 Cb28.9 ± 3.1 Ba44.4 ± 2.9 ABab61.1 ± 3.1 Ab132.0<0.01
0.50.0 ± 0.0 D11.1 ± 2.0 Ca35.6 ± 2.9 Ba56.7 ± 2.9 ABa81.1 ± 1.1 Aa160.0<0.01
F-21.820.814.829.8
p-<0.01<0.01<0.01<0.01
Table 3. Mean immediate mortality (% ± SE) of Tribolium castaneum larvae exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2) for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Table 3. Mean immediate mortality (% ± SE) of Tribolium castaneum larvae exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2) for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Exposure1 Day2 Days3 Days4 Days5 DaysFp
Dose (mg a.i./cm2)
0.012.2 ± 1.5 Cb7.8 ± 3.6 Cb21.1 ± 3.5 Bc38.9 ± 2.0 ABc66.7 ± 2.4 Ac30.3<0.01
0.055.6 ± 1.8 Cab13.3 ± 3.3 BCab26.7 ± 2.9 ABbc48.9 ± 3.1 Abc77.8 ± 4.3 Abc20.2<0.01
0.18.9 ± 2.6 Cab22.2 ± 4.0 BCa37.8 ± 5.2 ABb58.9 ± 5.1 Ab84.4 ± 4.8 Aab15.1<0.01
0.514.4 ± 2.9 Ca33.3 ± 4.1 Ba60.0 ± 4.4 ABa77.8 ± 4.0 Aa96.7 ± 1.7 Aa25.2<0.01
F4.35.812.220.012.3
p0.010.01<0.01<0.01<0.01
Table 4. Mean immediate mortality (% ± SE) of Sitophilus oryzae adults exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded. Where dashes exist, no analysis was performed.
Table 4. Mean immediate mortality (% ± SE) of Sitophilus oryzae adults exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded. Where dashes exist, no analysis was performed.
Exposure1 Day2 Days3 Days4 Days5 DaysFp
Dose (mg a.i./cm2)
0.010.0 ± 0.0 C0.0 ± 0.0 Cb8.9 ± 2.0 B25.6 ± 2.9 Ab45.6 ± 3.8 Ac96.4<0.01
0.050.0 ± 0.0 D0.0 ± 0.0 Db15.6 ± 1.8 C30.0 ± 5.3 Bb62.2 ± 2.8 Ab333.6<0.01
0.10.0 ± 0.0 C0.0 ± 0.0 Cb18.9 ± 4.8 B36.7 ± 2.9 Aab71.1 ± 3.1 Aab82.8<0.01
0.50.0 ± 0.0 D3.3 ± 1.7 Ca23.3 ± 2.4 B45.6 ± 2.4 ABa80.0 ± 1.7 Aa106.0<0.01
F-4.02.64.821.3
p-0.020.070.01<0.01
Table 5. Mean immediate mortality (% ± SE) of Rhyzopertha dominica adults exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Table 5. Mean immediate mortality (% ± SE) of Rhyzopertha dominica adults exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Exposure1 Day2 Days3 Days4 Days5 DaysFp
Dose (mg a.i./cm2)
0.010.0 ± 0.0 C2.2 ± 1.5 BC7.8 ± 2.8 B18.9 ± 2.6 A34.4 ± 3.8 Ab29.8<0.01
0.051.1 ± 1.1 C4.4 ± 2.4 BC8.9 ± 2.6 B25.6 ± 2.9 A40.0 ± 4.1 Aab22.0<0.01
0.12.2 ± 1.5 C8.9 ± 2.6 B15.6 ±2.4 AB26.7 ± 3.3 A43.3 ± 2.4 Aab22.9<0.01
0.54.4 ± 2.4 D10.0 ± 3.3 CD16.7 ± 4.1 BC32.2 ± 4.3 AB50.0 ± 4.1 Aa13.2<0.01
F1.42.22.62.23.1
p0.250.110.070.110.04
Table 6. Mean immediate mortality (% ± SE) of Acarus siro adults exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Table 6. Mean immediate mortality (% ± SE) of Acarus siro adults exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Exposure1 Day2 Days3 Days4 Days5 DaysFp
Dose (mg a.i./cm2)
0.010.0 ± 0.0 Dc7.8 ± 2.2 Cb24.4 ± 3.4 Bb38.9 ± 3.5 ABc65.6 ± 2.9 Ac67.7<0.01
0.055.5 ± 1.8 Cb17.8 ± 3.6 Bab33.3 ± 5.0 ABab50.0 ± 6.2 Abc74.4 ± 3.4 Abc20.2<0.01
0.110.0 ± 1.7 Cab27.8 ± 4.3 BCa38.9 ± 4.6 ABab62.2 ± 4.7 Aab82.2 ± 2.8 Aab14.5<0.01
0.517.8 ± 3.2 Ca35.6 ± 6.7 BCa54.4 ± 7.5 ABa72.2 ± 5.5 Aa92.2 ± 2.2 Aa13.4<0.01
F14.24.54.39.014.2
p<0.010.010.010.01<0.01
Table 7. Mean immediate mortality (% ± SE) of Acarus siro nymphs exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Table 7. Mean immediate mortality (% ± SE) of Acarus siro nymphs exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2), for 1, 2, 3, 4, and 5 days. Within each row, means followed by the same uppercase letter are not significantly different (in all cases DF = 4, 44, Tukey–Kramer HSD test at p = 0.05). Within each column, means that are followed by the same lower-case letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Exposure1 Day2 Days3 Days4 Days5 DaysFp
Dose (mg a.i./cm2)
0.012.2 ± 1.5 Cb17.8 ± 2.2 Bc27.8 ± 3.2 ABb37.8 ± 2.2 Ac45.6 ± 3.4 Ac53.2<0.01
0.057.8 ± 1.5 Ca24.4 ± 3.4 Bbc38.9 ± 3.9 ABab47.8 ± 3.6 ABbc56.7 ± 3.3 Abc22.2<0.01
0.113.3 ± 1.7 Da31.1 ± 3.1 Cab40.0 ± 3.3 BCa54.4 ± 3.4 ABab64.4 ± 4.4 Aab51.5<0.01
0.516.7 ± 1.7 Da36.7 ± 2.9 Ca46.7 ± 1.7 BCa61.1 ± 2.6 ABa73.3 ± 3.7 Aa73.2<0.01
F15.87.65.610.99.8
p<0.010.010.01<0.010.01
Table 8. ANOVA parameters for main effects and the associated interaction for delayed mortality of Tribolium castaneum adults and larvae, Sitophilus oryzae adults, Rhyzopertha dominica adults, and Acarus siro adults and nymphs (total DF = 202).
Table 8. ANOVA parameters for main effects and the associated interaction for delayed mortality of Tribolium castaneum adults and larvae, Sitophilus oryzae adults, Rhyzopertha dominica adults, and Acarus siro adults and nymphs (total DF = 202).
EffectDFSpecies
Source Fp
Species51.50.21
Dose38.1<0.01
Species × dose150.41.00
Table 9. Mean delayed mortality (% ± SE) of Tribolium castaneum adults and larvae, Sitophilus oryzae adults, Rhyzopertha dominica adults, and Acarus siro adults and nymphs exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2). Within each row, means followed by the same lowercase letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Table 9. Mean delayed mortality (% ± SE) of Tribolium castaneum adults and larvae, Sitophilus oryzae adults, Rhyzopertha dominica adults, and Acarus siro adults and nymphs exposed on concrete treated with chlorantraniliprole at four doses (0.01, 0.05, 0.1, and 0.5 mg a.i./cm2). Within each row, means followed by the same lowercase letter are not significantly different (in all cases DF = 3, 35, Tukey–Kramer HSD test at p = 0.05). Where no letters exist, no significant differences were recorded.
Dose (mg a.i./cm2)0.010.050.10.5DFFp
Species/Life Stage
T. castaneum adults91.0 ± 2.995.4 ± 3.197.8 ± 2.2100.0 ± 0.03, 352.50.08
T. castaneum larvae88.0 ± 4.293.5 ± 4.397.2 ± 2.8100.0 ± 0.03, 251.20.32
S. oryzae adults97.8 ± 2.298.2 ± 1.9100.0 ± 0.0100.0 ± 0.03, 350.70.58
R. dominica adults86.6 ± 3.4 b92.6 ± 2.6 ab96.7 ± 2.4 a98.6 ± 1.4 a3, 354.30.01
A. siro adults88.2 ± 6.092.6 ± 4.9100.0 ± 0.0100.0 ± 0.03, 321.90.15
A. siro nymphs90.3 ± 4.292.6 ± 3.894.4 ± 3.796.3 ± 3.73, 350.40.75
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Kavallieratos, N.G.; Boukouvala, M.C.; Nika, E.P.; Eleftheriadou, N.; Avtzis, D.N. Immediate and Delayed Mortality of Four Stored-Product Pests on Concrete Surfaces Treated with Chlorantraniliprole. Insects 2021, 12, 1088. https://doi.org/10.3390/insects12121088

AMA Style

Kavallieratos NG, Boukouvala MC, Nika EP, Eleftheriadou N, Avtzis DN. Immediate and Delayed Mortality of Four Stored-Product Pests on Concrete Surfaces Treated with Chlorantraniliprole. Insects. 2021; 12(12):1088. https://doi.org/10.3390/insects12121088

Chicago/Turabian Style

Kavallieratos, Nickolas G., Maria C. Boukouvala, Erifili P. Nika, Nikoleta Eleftheriadou, and Dimitrios N. Avtzis. 2021. "Immediate and Delayed Mortality of Four Stored-Product Pests on Concrete Surfaces Treated with Chlorantraniliprole" Insects 12, no. 12: 1088. https://doi.org/10.3390/insects12121088

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop