Abstract: Biological control programs in greenhouses increasingly resort to the release of several natural enemies simultaneously. In Uruguay, pest management in peppers is based on the release of Orius insidiosus and Amblyseius swirskii, to control Frankliniella occidentalis and Bemisia tabaci. Amblyseius swirskii can feed on both preys. Zoophytophagous predators not only feed on pests or plant food, but also on natural enemies with which they share prey (intraguild predation). Hence, the combined release of generalist predators could have a negative result in the control of the target pest. Thus, it was important to evaluate the compatibility of O. insidiosus and A. swirskii as predators of F. occidentalis. Studies carried out at Petri dishes level assessed: (1) the effect of the density and the composition of the prey on their predation by O. insidiosus, (2) the change of prey by O. insidiosus and (3) the effect of the genus of O. insidiosus on prey preference. Results show that if the relative densities of F. occidentalis and A. swirskii varied, O. insidiosus always changed to the most abundant prey. Male and female O. insidiosus preferred nymphs of F. occidentalis over A. swirskii, and females killed more prey than males. Since O. insidiosus fed on A. swirskii, it is advisable to be cautious when combining anthocorids and phytoseid mites for the F. occidentalis control. Studies at greenhouse will be necessary to clarify the final effect of both predators.
Keywords: anthocorids, intraguild predation, biological control, change of prey, preference.
Resumen: Los programas de control biológico en invernadero recurren cada vez más a la liberación de varios enemigos naturales en forma simultánea. En Uruguay, el manejo de plagas en pimiento se basa en la liberación de Orius insidiosus y Amblyseius swirskii, para controlar Frankliniella occidentalis y Bemisia tabaci. Amblyseius swirskii puede alimentarse de ambas presas. Los depredadores zoofitófagos no solo se alimentan de plagas o alimentos vegetales, sino también de enemigos naturales con quienes comparten presas (depredación intragremio). Por lo tanto, la liberación de depredadores generalistas podría dar resultado negativo en el control de la plaga objetivo. Por ello fue importante evaluar la compatibilidad entre O. insidiosus y A. swirskii como depredadores de F. occidentalis. A nivel de placas de Petri se estudió: (1) el efecto de la densidad y la composición de la presa sobre su depredación por O. insidiosus; (2) el cambio de presa por O. insidiosus, y (3) el efecto del género de O. insidiosus en la preferencia de presa. Se encontró que si las densidades relativas de F. occidentalis y A. swirskii variaban, O. insidiosus siempre cambiaba a la presa más abundante. Los machos y las hembras de O. insidiosus prefirieron las ninfas de F. occidentalis sobre A. swirskii, y las hembras mataron más presas que los machos. Dado que O. insidiosus depredó a A. swirskii, se recomienda precaución al combinar antocóridos y ácaros para el control de trips. Serán necesarios estudios en invernadero para esclarecer el efecto final de ambos depredadores.
Palabras clave: antocóridos, depredación intragremial, control biológico, cambio de presa, preferencia.
Resumo: Os programas de controle biológico com efeito de estufa dependem cada vez mais da liberação de vários inimigos naturais simultaneamente. No Uruguai, o manejo de pragas em pimentas é baseado na liberação de Orius insidiosus e Amblyseius swirskii, para o controle de Frankliniella occidentalis e Bemisia tabaci. Amblyseius swirskii pode se alimentar de ambas as presas. Predadores zoofitófagos não se alimentam apenas de pragas ou alimentos vegetais, mas também de inimigos naturais com os quais compartilham suas presas (predação intra-guilda). Portanto, a liberação de predadores generalistas pode controlar negativamente a praga alvo. Por esse motivo, foi importante avaliar a compatibilidade entre O. insidiosus e A. swirskii como predadores de F. occidentalis. Ao nível das placas de Petri, foram estudados: (1) o efeito da densidade e composição da presa na sua predação por O. insidiosus, (2) a mudança de presa por O. insidiosus e (3) o efeito -a do gênero de O. insidiosus em preferência de presa. Verificou-se que se as densidades relativas de F. occidentalis e A. swirskii variaram, O. insidiosus sempre mudou para a presa mais abundante. Machos e fêmeas de O. insidiosus preferiam ninfas de F. occidentalis a A. swirskii, e as fêmeas matavam mais presas do que os machos. Como O. insidiosus é anterior a A. swirskii, recomenda-se cautela ao combinar antocorídeos e ácaros para o controle de tripes. Estudos de estufa serão necessários para esclarecer o efeito final de ambos os predadores.
Palavras-chave: antocorídeos, predação intra-guilda, controle biológico, mudança de presa, preferência.
Compatibility of Orius insidiosus (Hemiptera: Anthocoridae) with Amblyseius swirskii (Acari: Phytoseiidae) for control of Flankliniella occidentalis (Thysanoptera: Thripidae) in pepper
Compatibilidad entre Orius insidiosus (Hemiptera: Anthocoridae) y Amblyseius swirskii (Acari: Phytoseiidae) en el control de Frankliniella occidentalis (Thysanoptera: Thripidae) en pimiento
Compatibilidade entre Orius insidiosus (Hemiptera: Anthocoridae) e Ambliseius swirskii (Acari: Phytoseiidae) no controle de Frankliniella occidentalis (Thysanoptera: Thripidae) em pimenta
Received: 09 June 2021
Accepted: 05 July 2021
Published: 29 July 2021
Corresponding author: email@example.com
The application of Integrated Pest Management programs is gaining more and more importance worldwide, as an approach that combines numerous sanitary techniques aiming to avoid economic damage caused by pests(1). The cornerstone of these programs is biological control(2), which is widely used in many countries and many situations, but has been developed especially in protected crops due to the high surface value of these productions(3). Control agents are periodically introduced to these crops, one or more times a year, so they can multiply in the crops, but without establishing permanently(4). In its implementation, several species of generalist predators are increasingly being released simultaneously against common pests(5)(6)(7). They are generally zoophytophagous predators, which is why they also include plant-provided food in their diet, but also other natural enemies(8)(9).
The species complementarity model suggests that herbivore mortality resulting from the combined action of different species of natural enemies is equal (additive) or higher (synergistic) than the sum of the mortality caused by each species of natural enemy(10). However, negative interactions between natural enemies, such as intraguild predation, facultative hyperparasitism, or interfering behavior, can affect herbivore suppression(11)(12). If negative interactions happen between control agents, rather than complementary effects, adding species can relieve phytophagous from the pressure of predation or parasitism(8). Negative interactions between natural enemies increase as diversity increases, making it necessary to decide between the release of a single superior species of natural enemies or multiple species against the herbivore pest(13). Intraguild predation is widespread in populations of natural enemies and occurs when one intraguild predator can negatively affect another, either by feeding on it or by competing for the shared resource (extraguild prey)(9). It can be unidirectional, with one species functioning as the top predator (i.e. intraguild) and the other as the intermediate predator (i.e. intraguild prey), or mutual, where the predators have the ability to consume each other(14)(15). Therefore, the combined release of generalist predators in these cases could have a negative result in the biological control of the target pest(16)(17).
In Uruguay, since 2013, numerous commercial producers carry out pest management of pepper cultivation under greenhouse based on the release of two predators, the mite Amblyseius swirskii (Athias) (Acarina: Phytoseiidae) used against whiteflies in tobacco, Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae), and the flower bugOrius insidiosus (Say) (Hemíptera: Anthocoridae) for the control of western flower thrips, Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae). Such management is proposed as an alternative to the traditional one based solely on the application of chemical insecticides and it follows the guidelines of the usual practices in European countries(18) and in the United States(19).
Frankliniella occidentalis is a serious pest, vector of diseases (TSWV, Tomato spotted wilt virus) and the cause of significant damage due to feeding and oviposition(20). Its control with chemical insecticides is difficult, since they lay their eggs inside the plant tissues, and both adults and larvae feed in protected places, such as flower buds, which protect the pest from the action of insecticides(21). Orius insidiosus feeds on thrips larvae and adults(22); while A. swirskii mainly kills whitefly eggs and nymphs, but can also prey on first-stage larvae of thrips(23). Some studies indicate that Orius spp. could also feed on mites(18)(24). Therefore, although the generalist nature of Orius spp. can be an advantage when considering greenhouse pest control, it can also be a source of concern, due to the possibility of interference with other natural enemies(25). Such is the case of A. swirskii(26).
Due to this, there was a special interest in studying the compatibility of A. swirskii and O. insidiosus when used for the control of F. occidentalis, so as to know if their interaction increases or reduces the plague suppression. A second objective was to determine how prey availability may affect the tendency of O. insidiosus to kill A. swirskii. For this, the abundance of F. occidentalis was varied in experiments under controlled conditions.
Colonies of F. occidentalis were established from individuals collected on pepper leaves and flowers (Capsicum annum L., Solanaceae) in the horticultural region of Salto (S 31°23′ - O 57°58′), Uruguay.
Thrips were multiplied in the Entomology laboratory at the Experimental Station of the Agronomy in Salto (EEFAS by its Spanish acronym) of the University of the Republic, following the protocol described by Steiner and Goodwin(27) and Espinosa and others(28). As plant substrate, bean seedlings were used (Phaseolus vulgaris L., Fabaceae), arranged in growth chambers in controlled conditions (25±1 ℃, 60±5% RH, 16:8 h L:D ). When the first leaves appeared, the petiole was cut off and placed in small glasses of water. The glasses were placed in glass containers (35 × 20 × 14 cm) with ventilated lids covered with fine mesh. Synchronized thrips cohorts were formed by placing adults on these leaves and transferring them to new leaves after 24 hours. These bean leaves containing the oviposition of the thrips were placed in boxes similar to those described above and kept for 6-7 days until the appearance of the second nymphal stage, or until 13-14 days when the adults appeared. These two states were used in the experiments. The individuals of A. swirskii and O. insidiosus were obtained from the Argentinian company Brometan. The A. swirskii mite was multiplied on pepper leaves, fed with eggs and nymphs of B. tabaci collected in commercial crops in Salto's horticultural region. The anthocorid O. insidiosus was reared using fresh bean pods as oviposition substrate and eggs of the flour moth, Ephestia kuehniella Zeller (Lepidoptera: Pyralidae) as prey, coming from the Production Unit of the Agronomy College. Each colony was placed in glass containers (35 × 20 × 14 cm) covered with low-density polyethylene (LDPE) stretch wrap with high transparency, in a climate-controlled chamber at 25 ± 1 ℃, 60 ± 5% RH 16:8 h (L: D).
Pepper plants (cvar Bilano type Lamuyo) and cowpea bean (Vigna unguiculata L. Walp.) grew individually in plastic pots of 20 cm in diameter and 10 cm deep, under controlled conditions (25 ℃ and 70% RH) with irrigation, in a polyethylene greenhouse of the Department of Plant Protection-Entomology at EEFAS, until they reached a suitable size for the experiments (20-30 cm in height).
The experiments with predators and thrips were carried out in an experimental unit that included a pepper leaf disk (6 cm in diameter) placed on filter paper moistened with distilled water. Said unit was placed in a 9.5 cm diameter x 1.5 cm deep Petri dish, vented through a hole in the lid covered with mesh (20 x 10 threads per cm2). During the 24-hour-long experiments, the plates were kept at 25 ± 1 ℃, 60 ± 5% RH, 16: 8 h (L: D). O. insidiosus adult females were deprived of food for 24 hours before their use.
To evaluate possible differences in the predation of F. occidentalis and A. swirskii by males and females of O. insidiosus, 10 adults of F. occidentalis and 10 adults of A. swirskii were placed with a male or female of O. insidiosus in the experimental units described above. Twelve repetitions were performed for each sex of O. insidiosus. The number of dead prey was counted 24 hours after the introduction of the anthocorids. To estimate prey mortality due to manipulation or possible predation of F. occidentalis by A. swirskii, 12 repetitions were carried out without the presence of O. insidiosus.
The predation capacity of O. insidiosus was evaluated on individuals of the second nymphal stage (6-7 days of life) and adults of F. occidentalis (13-14 days of life), and adults of A. swirskii, following the protocol described by Chow and others(26). Three densities were tested: 5, 10 and 20 preys (thrips or mites) per plate. Approximately one hour after the prey were placed, a single adult female of O. insidiosus was introduced. To avoid leaks, each plate was sealed with its lid and plastic wrap. At 24 hours, the number of dead preys inside the plates was counted.
Mortality due to handling was estimated from 10 repetitions for each type of prey (second stage or adult thrips) using 20 prey per plate without O. insidiosus. The handling was done with a fine tip brush.
Following the protocol established by Chow and others(26), the prey change of O. insidiosus females was evaluated by offering two combinations of prey: 5 F. occidentalis and 15 A. swirskii (1:3 ratio), 10 F. occidentalis and 10 A. swirskii (1:1 ratio), 15 F. occidentalis and 5 A swirskii (3:1 ratio). This experiment was repeated with second-stage nymphal and adult F. occidentalis individuals. In all cases, A. swirskii adults were used. Ten repetitions were completed for each relationship.
To do this, the required number of thrips was transferred to each plate, then the mites were incorporated and finally an O. insidiosus female. The dead preys were counted 24 hours after the introduction of the anthocorids.
The controls consisted of jointly depositing in the experimental units 20 F. occidentalis: 20 A. swirskii with no O. insidiosus. This experiment was conducted with second-stage nymphal and adult F. occidentalis individuals. In all cases, A. swirskii adults were used. Ten repetitions of each situation were performed.
All counts and proportions were checked for normality and homogeneity of variance (homoscedasticity). For the experiments with different prey densities, prey change and choice with both sexes of O. insidiosus, a two-way ANOVA was performed with “prey type” and “prey density” as factors to detect significant differences in the total number of dead and recovered prey between treatments. A one-way ANOVA was performed to compare the numbers of dead and recovered prey in controls. Tukey's honestly significant difference (HSD) test was used to determine significant differences between pairs of mean values after parametric tests.
Available Data: all the data set that supports the results of this study was published in this same article.
The mean number of prey killed by O. insidiosus females was about 30% higher than the prey killed by males for the two prey types (p = 0.023). The numbers of thrips and mites killed by the O. insidiosus males were not different from each other (p = 0.756), while the females killed more thrips than mites (p = 0.038) (Figure 1).
Mortality of A. swiskii and F. occidentalis in the control plates was less than 10% of each type of prey and did not vary between the two types of prey (p = 0.842).
Predation was affected by the type of prey (p = 0.013) and the density of the prey (p = 0.023). There was no interaction between prey type and density (p = 0.475). Predation of O. insidiosus increased with prey density (Figure 2). Prey mortality caused by the predator was higher than that registered in the controls (p = 0.019). In these, the mortality of both thrips and mites was less than 5% and did not vary with the prey type (p = 0.152).
Predation of F. occidentalis by O. insidiosus female increased with prey density (p = 0.047), as well as the predation of A. swirskii adults (p = 0.032). No differences were found between F. occidentalis adults and A. swirskii adults killed per Orius female (p = 0.613) at similar prey densities. On the other hand, the predation of F. occidentalis nymphs was greater than that of F. occidentalis and A. swirskii adults (p = 0.035), which did not differentiate between themselves.
The total predation of O. insidiosus was influenced by the type of prey, the number of prey and the numerical relationship between the prey. The females of O. insidiosus opted for the most abundant type of prey (p = 0.038), increasing consumption when there was a greater number of prey available (p = 0.045). When A. swirskii adults and F. occidentalis adults were available in equal numbers, the females of O. insidiosus showed no preference for one type of prey (p = 0.811) (Figure 3). However, when the adults of A. swirskii and the second nymphal stage of F. occidentalis were available in equal numbers, the females of O. insidiosus killed twice as many thrips as mites (p = 0.013) (Figure 4).
Prey mortality was very low in the control treatments, and the number of dead prey of A. swirskii and adults or the second nymphal stage of F. occidentalis did not differ for each of the prey combinations (p = 0.620) and the average mortality ranged from 4 to 8%.
The research studies that quantify the benefits of combining species of Orius and predatory mites for the control of F. occidentalis in greenhouse crops are few and their results vary since there are no differences between the release of a single agent compared to the release of both(26)(29)(30), to a greater reduction in the number of thrips if both agents are used simultaneously(31)(32).
In the present study, the intraguild predation model, which includes a higher predator (IG predator), an intermediate consumer (IG prey) and a shared resource(33), was confirmed in the interaction O. insidiosus - A. swirskii - F. occidentalis on a pepper leaf. Thus, Orius insidiosus killed the mite A. swirskii when it was available alone or in the presence of F. occidentalis. When the number of both preys was equal, O. insidiosus preferred the second nymphal stage of F. occidentalis over A. swirskii, and did not show differences between preys when considering adults of F. occidentalis and A. swirskii.
Our data show that the total and relative predation of F. occidentalis and/or A. swirskii by O. insidiosus depends on the type and number of prey available. When the number of individuals of the different types of prey was different, the preference in all cases was for the most abundant prey. Thus, when A. swirskii was the most abundant, that prey was preferred by O. insidiosus over F. occidentalis, which would indicate the possibility that O. insidiosus would replace the target prey, feeding on the other predator when thrips are scarce. Moreover, when A. swirskii is present in the crop, a significant increase in thrips would be necessary before O. insidiosus would prefer them. The statement by van Baalen and others(34) is reaffirmed, who state that changing prey can improve biological control by keeping predators on alternative prey when the target pests are rare, but it can also reduce control by distracting predators from attacking target pests, especially when they are not abundant.
These results demonstrate the need for caution when combining anthocorids and phytoseid mites for the control of F. occidentalis. Similar prey change patterns were found for O. insidiosus tested in combinations of A. degenerans and F. occidentalis(29), and of A. swirskii and F. occidentalis(26), both on greenhouse roses. This situation is also documented for other species of Orius against mites, such as O. majusculus(35), O. laevigatus(18)(24)(36) and O. tristicolor(25).
The results of this study were obtained by confining the two predators in a small plate. Caution is required when using small-scale laboratory experimental results to predict potential greenhouse interactions(37). Confrontations between O. insidiosus and A. swirskii are more likely in an experimental plate than in whole plants in a greenhouse. In addition, several factors may influence the intensity and outcome of intraguild predation, such as prey mobility, predation strategy, feeding specificity, relative prey size, and presence of extraguild prey(15)(37)(38)(39).
While much attention has been devoted to the influence of prey density and distribution on the feeding behavior of predators(40), these may also be influenced by the characteristics of the plants hosting their prey(41). Shipp and Whitfield(42) showed that the large number of trichomes in cucumber leaves, compared to pepper leaves, interfered with the search pattern of A. cucumeris (Oudemans). In addition, cutting leaves can affect the erection of the trichome and the chemical composition of the leaves, which in turn can influence the species observed(37).
It would be necessary to carry out complementary studies at the greenhouse level in order to clarify the final effect of using both predators together on the effectiveness of thrips control. According to Brodeur and others(43), intraguild predation by generalist predators is less important in greenhouses than in annual or perennial agroecosystems, since greenhouse crops are considered simple ecosystems with low biodiversity(44). The strength of the various interactions depends not only on the individual species involved but also on the suitability of the abiotic and biotic environment where the interactions take place. Interactions that appear very promising under controlled laboratory or greenhouse conditions have often been ineffective in the field due to unknown environmental constraints(45). Therefore, more research would be required for a better understanding of the interactions of change between anthochorids, predatory mites, and thrips in complex plant environments, and how these interactions would affect the suppression of thrips populations.
The effect of intraguild predation between O. insidiosus and A. swirskii requires caution if released simultaneously to control thrips F. occidentalis on peppers in Uruguay.
Author contribution statement: MEL
collected the data and wrote the article, prepared and edited the figures. CB
contributed to the writing of some sections of the article and directed the
investigation. OL performed the statistical analysis of the data and was
co-director of the research. LB, GG and LM collaborated on the research
following editor approved this article.
Valentina Mujica (https://orcid.org/0000-0002-9820-2879)
Nacional de Investigación Agropecuaria (INIA), Montevideo, Uruguay
We are grateful to the authorities of the Experimental Station of the Agronomy College (EEFAS by its Spanish acronym), and to the colleagues from the Department of Vegetal Protection in EEFAS and the Entomology Unit in Montevideo for their collaboration during the entire study period. This study was supported by a grant from the National Research and Innovation Agency (ANII/INNOVAGRO) that funded a project entitled “Contribution to the biological control of pests of horticulture in the region of Salto.”