Home Life Sciences Importance of wildflowers in Orius insidiosus (Heteroptera: Anthocoridae) diet
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Importance of wildflowers in Orius insidiosus (Heteroptera: Anthocoridae) diet

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Published/Copyright: April 4, 2024

Abstract

The addition of non-crop floral resources is known to improve the fitness of many beneficial arthropods. Orius insidiosus (Say; Heteroptera: Anthocoridae) is a predator of several economically important pests and is known to feed on pollen. Spanish needles, Bidens alba L., and Leavenworth’s tickseed, Coreopsis leavenworthii Torrey & Gray (both Asteraceae), are two Florida native wildflowers that may serve as sources of pollen beneficial to O. insidiosus. The current study investigated the effects of adding flowers from C. leavenworthii and B. alba to the diet of captive O. insidiosus on longevity, nymphal development time, and cannibalism. A mixed diet of flowers and thrips prey increased O. insidiosus adult female longevity. Nymphal development time was reduced when B. alba was added to thrips when compared to a diet of thrips alone. Interestingly, cannibalism was low in all instances, suggesting a negligible effect of cannibalism on O. insidiosus except perhaps in extreme situations. These results indicate that B. alba and C. leavenworthii flowers can increase longevity and fitness of O. insidiosus, thus providing support for the use of these plants to enhance natural enemy services.

Resumen

Se sabe que la adición de recursos florales no agrícolas mejora la aptitud de muchos artrópodos beneficiosos. Orius insidiosus (Say; Heteroptera: Anthocoridae) es un depredador de varias plagas económicamente importantes y se sabe que se alimenta de polen. El mazote blanco, Bidens alba L., y la semilla de garrapata de Leavenworth, Coreopsis leavenworthii Torrey & Gray (ambas Asteraceae), son dos flores silvestres nativas de la Florida que pueden servir como fuentes de polen beneficioso para O. insidiosus. El estudio actual investigó los efectos de agregar flores de C. leavenworthii y B alba a la dieta de O. insidiosus en cautiverio sobre su longevidad, tiempo de desarrollo ninfal y canibalismo. Una dieta mixta de flores y trips aumentó la longevidad de las hembras adultas de O. insidiosus. El tiempo de desarrollo ninfal se redujo cuando se añadió B. alba a los trips en comparación con una dieta de trips solos. Curiosamente, el canibalismo fue bajo en todos los casos, lo que sugiere un efecto insignificante de canibalismo en O. insidiosus, excepto quizás en situaciones extremas. Estos resultados indican que las flores de B. alba y C leavenworthii pueden aumentar la longevidad y la aptitud de O. insidiosus, brindando así apoyo para el uso de estas plantas en la mejora de los servicios contra los enemigos naturales.

1 Introduction

Non-crop floral resources are used to increase abundance and fitness of natural enemies by providing hosts for parasitoids, prey for predators, and additional food resources such as pollen or nectar (Symondson et al. 2002; Wong and Frank 2013). This is particularly critical for omnivorous predators that often benefit from a diet of both prey and plant material (Coll and Guershon 2002; Leon-Beck and Coll 2007; Wong and Frank 2013). Flowering plants can therefore be considered in conservation biological control strategies in the form of banker plants, flower strips or hedgerow plantings to increase recruitment and survival of predators, particularly in monoculture systems with or without a time-limited resource of suitable pollen (Coll and Guershon 2002; Lundgren et al. 2009; Wong and Frank 2013; Waite et al. 2014).

Orius species (Hemiptera: Anthocoridae), also called minute pirate bugs, are generalist predators that feed primarily on thrips but also are known to feed and successfully reproduce on other pests affecting vegetable crops such as whiteflies, aphids, and mites (Lundgren et al. 2009; Wong and Frank 2013; Bernardo et al. 2017). Several species are known to feed on pollen at the nymphal and adult stage in addition to prey, which is proposed to affect survival and development time as well as reduce cannibalism (Kiman and Yeargan 1985; Coll and Guershon 2002; Leon-Beck and Coll 2007; Calixto et al. 2013; Wong and Frank 2013; Bueno et al. 2014). In a previous study, a diet of pollen from pepper Capsicum annuum L. cv ‘Black pearl’ (Solanaceae) combined with thrips increased Orius insidiosus (Say) longevity and size and decreased nymphal development time (Wong and Frank 2013). There is also evidence that the addition of pollen may reduce cannibalism, which has been described as a potential limiting factor in mass rearing of O. insidiosus for commercial use (Leon-Beck and Coll 2007; Calixto et al. 2013; Bueno et al. 2014).

Bidens alba L. and Coreopsis leavenworthii Torrey & Gray are two Asteraceae host plants of Orius spp. native to Florida that have been shown to increase natural enemy and pollinator services (Funderburk 2009; Tyler-Julian et al. 2018; Abdelmaksoud et al. 2020). In addition, these plant species serve as hosts for less damaging native thrips species (Thysanoptera: Thripidae) including Frankliniella bispinosa Morgan and Frankliniella tritici (Fitch), which have been shown to outcompete the worldwide pest F. occidentalis (Pergande) (Baez et al. 2004; Reitz et al. 2006; Paini et al. 2008; Northfield et al. 2011). For this reason, B. alba and C. leavenworthii are potential candidates to be used as companion plants to enhance O. insidiosus fitness (Norcini et al. 2009; Tyler-Julian et al. 2018). Nevertheless, there is limited research documenting the direct effects of B. alba and C. leavenworthii on the overall fitness of Orius spp., perhaps due to their perceived status as weeds. There remains a need to investigate their potential to improve O. insidiosus fitness and abundance, and to provide justification for their use in improving conservation biological control of thrips and other pest species.

2 Materials and methods

2.1 Insect colonies

Thrips (Frankliniella tritici) colonies were established with wild populations collected in Gadsden county, Florida and identified to species according to Sprague et al. (2018). Adult thrips were reared in plastic containers (16.2 × 17.7 × 9.3 cm; Rubbermaid, Atlanta, Georgia) vented with thrips-proof mesh (BioQuip, Rancho Dominguez, California) and were provided with green beans washed in a 5 % bleach solution and air dried for food and oviposition. Colonies were kept in an incubator at 25 °C, relative humidity (RH) 60–70 %, and 12:12 h (L:D) photoperiod.

O. insidiosus colonies were established with wild populations collected in Gadsden county, Florida. Adult O. insidiosus were identified based on the melanization of the femora, basal antennal segments, and wing cuneus (Shapiro et al. 2009). Adult O. insidiosus were housed in plastic containers (18.7 × 18.7 × 14.6 cm; Rubbermaid, Atlanta, Georgia) vented with thrips-proof mesh and were provided with F. tritici as prey and flowers from B. alba and L. indica. Bean pods were provided as supplementary food and an oviposition substrate. Colonies were kept in an incubator at 21.1 °C, RH 60–70 %, and 12:12 h (L:D) photoperiod.

2.2 Plants

B. alba (identified according to Khamare et al. 2019) seeds were collected from wild plants in Gadsden county, Florida, and C. leavenworthii seeds were purchased (Florida Wildflower Cooperative, Crescent City, Florida). Seeds were planted in greenhouse trays (53.3 × 27.9 × 6.3 cm; Growers Solution, Cookville, Tennessee) and seedlings were transplanted into 3.8 L nursery pots. The plants were irrigated by hand and fertilized every 2 weeks with an all-purpose plant food (Scotts Miracle-Gro Company, Marysville, Ohio).

2.3 Diet assays

All assays were carried out in a completely randomized design and were performed in growth chambers at 21.1 °C, RH 60–70 %, and 12:12 h (L:D) photoperiod. Nymphs were removed from the colony and put into a separate container and checked daily. As adult females emerged, they were removed and placed into another container. Each treatment was applied to an individual O. insidiosus contained in a Petri dish (100 mm diameter; Fisher Scientific, Hampton, New Hampshire) lined with filter paper (9.0 cm diameter; Fisher Scientific, Hampton, New Hampshire) and with a moistened cotton wick for water. The top of the Petri dish was vented with a 2.54 × 2.54 cm hole covered with thrips-proof mesh. The Petri dishes were sealed with Parafilm® (Bemis Company, Neenah, Wisconsin) wrapped around the lid to prevent insects from escaping.

2.3.1 Female survival

One adult female O. insidiosus with unknown mating status was placed in a Petri dish in the 24 h after adult emergence and given one of five diets: (1) C. leavenworthii and F. tritici, (2) C. leavenworthii only, (3) B. alba and F. tritici, (4) B. alba only, or (5) F. tritici only. For both C. leavenworthii and B. alba the disc flowers from pseudanthia collected the same day were extracted and placed in the Petri dish. There were nine replicates for each treatment. In the diets with thrips, approximately 20–30 adult and larval F. tritici were supplied every day. In the diets with flowers, three flowers per Petri dish were provided every other day. Insects were aspirated out of the flowers to ensure none were present in the treatments with flowers only. The Petri dishes were checked every 24 h for 20 days, and the O. insidiosus females were recorded as dead or alive.

2.3.2 Nymphal development

A single unsexed first instar nymph (<24 h after hatching) was placed into a Petri dish with one of the five different diets described previously. There were 20 replicates for each treatment. The Petri dishes were checked every 24 h until O. insidiosus adults emerged. The days to adult were calculated as the date of the start of the assay subtracted from the date of adult emergence.

2.3.3 Cannibalism

One female O. insidiosus was placed into a Petri dish and starved for 24 h with no flowers or prey. After 24 h, each was given one of six diets: (1) C. leavenworthii + F. tritici + 5 O. insidiosus nymphs, (2) C. leavenworthii + 5 O. insidiosus nymphs, (3) B. alba + F. tritici + 5 O. insidiosus nymphs, (4) B. alba + 5 O. insidiosus nymphs, (5) F. tritici + 5 O. insidiosus nymphs, and (6) 5 O. insidiosus nymphs only. There were 10 replicates for each treatment. Various nymphal stages were used as supply was limited due to availability in the rearing. The number of O. insidiosus nymphs dead or alive was recorded after 2, 4, 8, 16, 24, and 48 h.

2.4 Statistical analysis

All data met the assumptions of normality and homogeneity of variance. Statistical analysis of female survival data was conducted with the statistical software R (R 3.5.1, RStudio, Boston, Massachusetts). Female survival data were analyzed using Cox’s proportional hazards model to investigate the association between the survival time of O. insidiosus females and diet treatment (Cox 1972). Data from nymphal development and cannibalism assays were analyzed using ANOVA to determine the effects of diet treatment on days to adult and the proportion of cannibalism, respectively (PROC ANOVA, SAS 9.4, SAS Institute Inc., Cary, North Carolina). Pearson’s chi-square test was conducted on data from the cannibalism assays pooled for all diet treatments.

3 Results

3.1 Female survival

There was a significant effect of adding C. leavenworthii and B. alba in a diet for adult female O. insidiosus survivorship (LR = 21, d.f. = 4, P < 0.001) (Figure 1). Adults given diets containing C. leavenworthii flowers + F. tritici, B. alba + F. tritici, and C. leavenworthii flowers alone survived significantly longer (11.56 ± 12.9, 14.89 ± 0.96, and 12.89 ± 1.06 days, respectively) than those with a diet of B. alba flowers only or F. tritici thrips only (7.44 ± 1.32, 8.00 ± 0.95 days, respectively). A diet of B. alba flowers only did not differ from a diet of thrips alone.

Figure 1: 
Survival distribution of adult female Orius insidiosus when fed a diet of thrips F
rankliniella
 tritici, flowers of Bidens alba only, flowers of B. alba + F. tritici, flowers of Coreoposis leavenworthii only, or flowers of C. leavenworthii + F. tritici as a function of hours until event up to 480 h (20 days).
Figure 1:

Survival distribution of adult female Orius insidiosus when fed a diet of thrips F rankliniella  tritici, flowers of Bidens alba only, flowers of B. alba + F. tritici, flowers of Coreoposis leavenworthii only, or flowers of C. leavenworthii + F. tritici as a function of hours until event up to 480 h (20 days).

3.2 Nymphal development

All 100 nymphs survived to adulthood. There was a significant difference among treatments for the nymphal development time (F 4,95 = 3.62; P = 0.0086). O. insidiosus fed with a diet of B. alba and F. tritici had a reduced development time as compared to O. insidiosus nymphs provided with a diet of F. tritici alone (P < 0.05). O. insidiosus fed on diets with C. leavenworthii, C. leavenworthii + F. tritici, or B. alba alone did not differ in development time as compared to the O. insidiosus fed on thrips only (P > 0.05) (Figure 2).

Figure 2: 
Adult emergence time (mean ± SEM days) for Orius insidiosus nymphs when fed a diet of thrips F
rankliniella
 tritici, Bidens alba only, B. alba + F. tritici, Coreopsis leavenworthii only, or C. leavenworthii + F. tritici. Different lowercase letters indicate a significant difference among treatments (P < 0.05).
Figure 2:

Adult emergence time (mean ± SEM days) for Orius insidiosus nymphs when fed a diet of thrips F rankliniella  tritici, Bidens alba only, B. alba F. tritici, Coreopsis leavenworthii only, or C. leavenworthii F. tritici. Different lowercase letters indicate a significant difference among treatments (P < 0.05).

3.3 Cannibalism

Cannibalism events were quite rare throughout all the experiment, with only 10 % for the O. insidiosus females provided with O. insidiosus nymphs only. After 48 h, there were no significant differences in instances of cannibalism of O. insidiosus nymphs or adults for any of the diet treatments (chi-square = 6.6554; d.f. = 5; P = 0.2476) (Figure 3).

Figure 3: 
Proportion of Orius insidisous cannibalism after 48 h when fed a diet of thrips F
rankliniella
 tritici, Bidens alba only, B. alba + F. tritici, Coreopsis leavenworthii only, C. leavenworthii + F. tritici, or a control with no food. The proportion was determined by the number of nymphs cannibalized divided by the total number of nymphs in each treatment (5). There was no significant differences among treatments (P > 0.05).
Figure 3:

Proportion of Orius insidisous cannibalism after 48 h when fed a diet of thrips F rankliniella  tritici, Bidens alba only, B. alba + F. tritici, Coreopsis leavenworthii only, C. leavenworthii + F. tritici, or a control with no food. The proportion was determined by the number of nymphs cannibalized divided by the total number of nymphs in each treatment (5). There was no significant differences among treatments (P > 0.05).

4 Discussion

The current study suggests that adding flowers from B. alba and C. leavenworthii has a positive impact on O. insidiosus fitness. However, the effects varied by treatment: while B. alba reduced nymphal development time and increased survival when combined with thrips prey, C. leavenworthii increased O. insidiosus female survival by itself as compared to a diet with thrips only. However, no effect on development time was found for C. leavenworthi. Survival of O. insidiosus females fed with thrips and flowers (15 days for B. alba and thrips and 12 days for C. leavenworthi and thrips) was slightly higher than from other studies (14 days on average in Calixto et al. (2013) with a commercial mix of pollen from various flowers, 8 days in Wong and Frank (2013) with pepper flowers). Similarly, development times of O. insidiosus nymphs in this study (from 9.5 days for B. alba + thrips to 12 for thrips only) were longer than in Wong and Frank (2013) (7–8 days) but on a similar range compared with other studies (10–13 days in Mendes et al. (2002), 11–15 days in Bernardo et al. (2017)).

Previous studies have demonstrated the benefits of adding pollen to the diet of Orius spp. Wong and Frank (2013) and Waite et al. (2014) found that the addition of pollen from ornamental pepper cultivars (cv. ‘Black Pearl’ and ‘Purple Flash’) increased O. insidiosus survival and decreased nymphal development time, and a pollen blend of several plants including Eucalyptus sp. (Myrtaceae), Bidens pilosa L. (Asteraceae), and Citrus sp. (Rutaceae) shortened nymphal development compared to a diet of prey only (Bernardo et al. 2017). In this study, because both plants were Asteraceae, we did not separate the pollen that are intricated within the tiny disc flowers. Therefore, we cannot rule out that Orius may also have fed on other parts of the flower in addition to the pollen. The results from this study regarding O. insidiosus female survival differ from that of previous studies where survival was not affected by the addition of pollen to a diet when compared to a diet of thrips prey or pollen only (Wong and Frank 2013). However, in all cases, including in the current study, Orius spp. fed a diet containing pollen have similar or increased longevity. The extent to which these effects occur may be dependent on the nutritional value of pollen, which stresses the importance of choosing appropriate pollen sources (Waite et al. 2014; Bernardo et al. 2017).

O. insidiosus is a common and popular commercial biological control agent used against F. occidentalis and other pests. As an omnivorous predator, they are known to utilize plant materials in addition to prey. When prey availability is low, however, many predators exhibit cannibalistic behaviors, including O. insidiosus (Leon-Beck and Coll 2007; Bueno et al. 2014). This study hypothesized that cannibalism would be reduced with the addition of B. alba and C. leavenworthii flowers than on prey alone as supplementing with plant material is expected to benefit nutrition (Leon-Beck and Coll 2007). Results, however, showed no difference in cannibalism amongst O. insidiosus because of diet and are supported by a previous study by Leon-Beck and Coll (2007) who found no differences in cannibalism occurrence in another Orius species, Orius laevigatus (Fieber), when provided with prey, pollen, or both. Interestingly, there was very low cannibalism (≤10 %) in all treatments, including no prey or pollen, which suggests cannibalism among O. insidiosus may be minimal except in cases of extreme stress that may occur in industrial rearing (i.e., low food availability combined with lack of shelter or hiding spots (Bueno et al. 2014)).

The use of B. alba and C. leavenworthii flowers to supplement a prey diet can increase O. insidiosus survival and decrease nymphal development time, with some variations, depending on the pollen source. A shorter development time is considered a desirable life history trait for a biological control agent as it reduces the non-reproductive period and the stage where the individual is the most susceptible to intra-guild predation or cannibalism, it also allows for the rapid deployment of the agent to control the pest population (Facon 2011; Wong and Frank 2013; Sentis et al. 2022). In addition, shorter development time and higher adult survivorship is usually corelated to higher fecundity in Orius sp. (Tommasini et al. 2004: Calixto et al. 2013). The results from this study suggest that these two plants may be valuable assets for increasing and sustaining O. insidiosus populations through conservation biological control and augmentative biological control in the case of mass rearing.


Corresponding author: Xavier Martini, Department of Entomology and Nematology, University of Florida North Florida Research and Education Center, Quincy, FL 32351, USA, E-mail:

Funding source: Southern SARE

Award Identifier / Grant number: GS18-191

Funding source: Southern SARE

Award Identifier / Grant number: OS20-137

  1. Research ethics: Not applicable.

  2. Author contributions: Conceptualization IS, XM; Methodology: IS; Formal analysis IS; Investigation IS; Resources XM; Writing IS; Review and Editing IS, XM. The authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The authors state no conflict of interest.

  4. Research funding: This work was funded by grants obtained by Southern SARE awarded to XM and IS (GS18-191 and OS20-137).

  5. Data availability: The raw data can be obtained on request from the corresponding author .

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Received: 2024-02-26
Accepted: 2024-02-27
Published Online: 2024-04-04

© 2024 the author(s), published by De Gruyter on behalf of the Florida Entomological Society

This work is licensed under the Creative Commons Attribution 4.0 International License.

Articles in the same Issue

  1. Frontmatter
  2. Research Articles
  3. Distribution and dispersal of adult spotted wing drosophila, Drosophila suzukii (Diptera: Drosophilidae), in organically grown strawberries in Florida
  4. A comparison of the capture of non-target arthropods between control methods and monitoring traps of Anastrepha ludens in citrus agroecosystems
  5. Development of microsatellite markers for colony delineation of the invasive Asian subterranean termite (Blattodea: Rhinotermitidae) in South Florida and Taiwan
  6. Biology and life table of Oligonychus punicae Hirst (Trombidiformes: Tetranychidae) on three host plants
  7. Relative captures and detection of male Ceratitis capitata using a natural oil lure or trimedlure plugs
  8. Evaluation of HOOK SWD attract-and-kill on captures, emergence, and survival of Drosophila suzukii in Florida
  9. Rearing Neoseiulus cucumeris and Amblyseius swirskii (Mesostigmata: Phytoseiidae) on non-target species reduces their predation efficacy on target species
  10. Response of male Bactrocera zonata (Diptera: Tephritidae) to methyl eugenol: can they be desensitized?
  11. Monitoring of coccinellid (Coleoptera) presence and syrphid (Diptera) species diversity and abundance in southern California citrus orchards: implications for conservation biological control of Asian citrus psyllid and other citrus pests
  12. Topical treatment of adult house flies, Musca domestica L. (Diptera: Muscidae), with Beauveria bassiana in combination with three entomopathogenic bacteria
  13. Laboratory evaluation of 15 entomopathogenic fungal spore formulations on the mortality of Drosophila suzukii (Diptera: Drosophilidae), related drosophilids, and honeybees
  14. Effect of diatomaceous earth on diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae), larval feeding and survival on cabbage
  15. Bioactivity of seed extracts from different genotypes of Jatropha curcas (Euphorbiaceae) against Spodoptera frugiperda (Lepidoptera: Noctuidae)
  16. Assessment of sugarberry as a host tree of Halyomorpha halys (Hemiptera: Pentatomidae) in southeastern USA agroecosystems
  17. The importance of multigeneration host specificity testing: rejection of a potential biocontrol agent of Nymphaea mexicana (Nymphaeaceae) in South Africa
  18. Endophytic potential of entomopathogenic fungi associated with Urochloa ruziziensis (Poaceae) for spittlebug (Hemiptera: Cercopidae) control
  19. The first complete mitogenome sequence of a biological control agent, Pseudophilothrips ichini (Hood) (Thysanoptera: Phlaeothripidae)
  20. Exploring the potential of Delphastus davidsoni (Coleoptera: Coccinellidae) in the biological control of Bemisia tabaci MEAM 1 (Hemiptera: Aleyrodidae)
  21. Behavioral responses of Ixodiphagus hookeri (Hymenoptera; Encyrtidae) to Rhipicephalus sanguineus nymphs (Ixodida: Ixodidae) and dog hair volatiles
  22. Illustrating the current geographic distribution of Diaphorina citri (Hemiptera: Psyllidae) in Campeche, Mexico: a maximum entropy modeling approach
  23. New records of Clusiidae (Diptera: Schizophora), including three species new to North America
  24. Photuris mcavoyi (Coleoptera: Lampyridae): a new firefly from Delaware interdunal wetlands
  25. Bees (Hymenoptera: Apoidea) diversity and synanthropy in a protected natural area and its influence zone in western Mexico
  26. Temperature-dependent development and life tables of Palpita unionalis (Lepidoptera: Pyralidae)
  27. Orchid bee collects herbicide that mimics the fragrance of its orchid mutualists
  28. Importance of wildflowers in Orius insidiosus (Heteroptera: Anthocoridae) diet
  29. Bee diversity and abundance in perennial irrigated crops and adjacent habitats in central Washington state
  30. Comparison of home-made and commercial baits for trapping Drosophila suzukii (Diptera: Drosophilidae) in blueberry crops
  31. Miscellaneous
  32. Dr. Charles W. O’Brien: True Pioneer in Weevil Taxonomy and Publisher
  33. Scientific Notes
  34. Nests and resin sources (including propolis) of the naturalized orchid bee Euglossa dilemma (Hymenoptera: Apidae) in Florida
  35. Impact of laurel wilt on the avocado germplasm collection at the United States Department of Agriculture, Agricultural Research Service, Subtropical Horticulture Research Station
  36. Monitoring adult Delia platura (Diptera: Anthomyiidae) in New York State corn fields using blue and yellow sticky cards
  37. New distribution records and host plants of two species of Hypothenemus (Coleoptera: Curculionidae: Scolytinae) in mangrove ecosystems of Tamaulipas, Mexico
  38. First record of Trichogramma pretiosum parasitizing Iridopsis panopla eggs in eucalyptus in Brazil
  39. Spodoptera cosmioides (Lepidoptera: Noctuidae) as an alternative host for mass rearing the parasitoid Palmistichus elaeisis (Hymenoptera: Eulophidae)
  40. Effects of biochar on ambrosia beetle attacks on redbud and pecan container trees
  41. First report of Diatraea impersonatella (Lepidoptera: Crambidae) on sugarcane (Saccharum officinarum L.) in Honduras
  42. Book Reviews
  43. Kratzer, C. A.: The Cicadas of North America
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