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Article

Low Incidence of Avian Predation on the Brown Marmorated Stink Bug, Halyomorpha halys (Hemiptera: Pentatomidae), in Southeastern Orchard Systems

by
Erin E. Grabarczyk
1,2,*,
Ted E. Cottrell
3,
Jason M. Schmidt
4 and
P. Glynn Tillman
1
1
Southeast Watershed Research Laboratory, USDA-ARS, Tifton, GA 31793, USA
2
Department of Biology, Valdosta State University, Valdosta, GA 31698, USA
3
Southeastern Fruit and Tree Nut Research Laboratory, USDA-ARS, Byron, GA 31008, USA
4
Department of Entomology, University of Georgia, Tifton, GA 31793, USA
*
Author to whom correspondence should be addressed.
Insects 2023, 14(7), 595; https://doi.org/10.3390/insects14070595
Submission received: 13 May 2023 / Revised: 19 June 2023 / Accepted: 29 June 2023 / Published: 1 July 2023
(This article belongs to the Special Issue Biological Control in Temperate Orchards)
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Abstract

:

Simple Summary

Stink bugs (Hemiptera: Pentatomidae) are an insect pest that cause damage to pecan and peach fruits. In forests that surround fruit and tree nut orchards, insectivorous birds may consume stink bug pests, such as the brown marmorated stink bug (Halyomorpha halys). In this study, we mist-netted birds, collected avian fecal samples, and monitored brown marmorated stink bugs in forests that surround peach and pecan orchards in Georgia, USA. We used PCR to screen avian fecal samples for brown marmorated stink bug DNA, which is evidence of their consumption by birds. We found three bird species consumed brown marmorated stink bugs, including Northern cardinal (Cardinalis cardinalisis), Tufted titmouse (Baeolophus bicolor), and Carolina wren (Thryothorus ludovicianus). Overall, the number of avian fecal samples with brown marmorated stink bug DNA was low, which may be due to the short retention time of prey for birds. Future studies should explore whether birds contribute to the biological control of additional pecan and pecan insect pests.

Abstract

In many agroecosystems, brown marmorated stink bugs (Halyomorpha halys) (Hemiptera: Pentatomidae) are polyphagous pests that cause significant economic losses to numerous crops every year. Insectivorous birds may provide a means of sustainable predation of invasive pests, such as H. halys. In forest margins surrounding peach, pecan, and interplanted peach–pecan orchards, we monitored H. halys populations with pheromone-baited traps, mist-netted birds, and collected avian fecal samples for molecular gut content analysis. We screened 257 fecal samples from 19 bird species for the presence of H. halys DNA to determine whether birds provide the biological control of this pest. Overall, we found evidence that four birds from three species consumed H. halys, including Northern cardinal (Cardinalis cardinalisis), Tufted titmouse (Baeolophus bicolor), and Carolina wren (Thryothorus ludovicianus). Halyomorpha halys captured in traps increased over time but did not vary by orchard type. Although incidence of predation was low, this may be an underestimate as a result of our current avian fecal sampling methodology. Because birds are members of the broader food web, future studies are needed to understand avian ecosystem services, especially in terms of pest control, including H. halys and other pest species.

1. Introduction

Brown marmorated stink bugs (Halyomorpha halys) (Stål) (Hemiptera: Pentatomidae) are an invasive pest that aggregates in urban and agricultural areas, including orchards [1,2,3]. In orchard agroecosystems, H. halys disperse between fruit trees and surrounding unmanaged habitats, foraging on available foods, which results in significant economic damage [4,5,6,7,8,9]. Control of H. halys often relies on chemical spray applications targeted on trees within orchards [1,2,3]. As a result, management practices are usually applied within the boundaries of crop fields and orchards, while the surrounding non-crop habitats, such as forests, woodlands, and hedgerows, which can support populations of H. halys, are left untouched. Because H. halys disperse between agricultural and surrounding habitats, solutions for their management should seek strategies to include surrounding non-crop habitats.
Insectivorous birds that inhabit forest habitats surrounding orchards may provide biological control of arthropod pests [10,11]. Molecular gut content analysis of avian fecal material (i.e., gut content) is a minimally disruptive approach, where samples are easily collected during routine mist-netting procedures in and around agricultural areas [12]. To date, analysis of avian pest consumption ranges from detection of a single prey species [13,14] to DNA metabarcoding analysis that captures diet breadth [15,16,17]. Although more research is warranted, some general patterns of avian pest control in orchard systems have emerged. In macadamia orchards, an analysis of eleven bird species found overlaps in diet diversity and consumption of five major insect pest species, including pentatomids [15]. In this system, as pest populations increased in orchards, consumption of insect pests by birds increased as well [15]. A DNA-based approach was used to detect whether birds forage on codling moth (Cydia pomonella) (L.) (Lepidoptera: Tortricidae) in organic apple orchards, however, detection was extremely low; only one species, the brown-headed cowbird (Molothrus ater), ate codling moths [13]. To date, no research has focused specifically on birds as biocontrol agents of the brown marmorated stink bug, a significant agricultural pest that is rapidly expanding across the southeastern USA [18].
The objective of this study was to assess bird contributions to the biological control of the brown marmorated stink bug, H. halys, in forest habitats adjacent to commercial pecan and peach orchards. During 2021–2022, we monitored H. halys populations with pheromone-baited traps at nine orchards in central Georgia, USA. Simultaneously, we mist-netted birds and collected avian fecal samples for molecular gut content analysis. We used targeted PCR to determine the presence or absence of H. halys DNA in avian fecal samples and compared counts of H. halys captured in forests surrounding orchards to their consumption by birds.

2. Materials and Methods

2.1. Field Methods

To capture and monitor H. halys, we used yellow pyramid traps, baited with aggregation pheromones highly attractive to nymphs and adults of H. halys, within approximately a 3 m2 area [19,20,21,22,23]. Two pheromone-baited traps were set along forest edge adjacent to peach and pecan orchards at nine study sites (n = 18 traps) from 1 June 2021 to 1 September 2021, and at seven of the same nine study sites (n = 14 traps) from 5 May 2022 to 6 July 2022. Three of the sites were pecan orchards, three were peach orchards, three were interplanted pecan and peach orchards, and all were located in Peach County, Georgia, USA (Figure 1A,B). Traps were placed at least 50 m apart in forests along the forest-orchard border (Figure 1C). Pheromone-baited traps consisted of a 2.8-L clear plastic PET jar with a screw-top lid (10.2-mm diameter) to collect insects (United States Plastic Corp., Lima, OH). Collection jars were placed on top of a 1.22 m yellow pyramid trap base [24]. The commercially available pheromone lures for H. halys includes the aggregation pheromone of H. halys, a combination of stereoisomers (3S,6S,7R,10S)-10,11-epoxy-1-bisabolen-3-ol and (3R,6S,7R,10S)-10,11-epoxy-1 bisabolen-3-ol (PHER), and a synergist, methyl (2E,4E,6Z)-2,4,6-decatrienoate (MDT), which is the aggregation pheromone of Plautia stali (Scott) (Hemiptera: Pentatomidae). Therefore, to increase capture success of H. halys, we baited traps with a set of two commercial aggregation lures: H. halys male aggregation pheromone (PHER) and the synergist (MDT) (Trécé Pherocon, Adair, OK, USA). Inside each trap, we placed a kill strip (10% λ-cyhalothrin and 13% piperonyl butoxide) (Saber extra insecticide ear tags, Sagebrush Tags, De Smet, SD) to decrease the likelihood of stink bug escape [25]. Once per week, captured stink bugs were removed from traps and stored in resealable bags at the Southeast Watershed Research Laboratory in Tifton, Georgia. Pheromone baits were replaced every other week. Identification of H. halys was based on Rice et al. [3]. Pesticide application (fungicide, insecticide, and herbicide) at study sites followed recommendations for commercial peach and pecan production published by the University of Georgia extension guidelines [26,27].
From 8 June 2021 to 26 August 2021 and from 5 May 2022 to 27 June 2022, birds that inhabited forests surrounding focal orchards were captured via mist net and fecal gut content samples were collected. Each morning of netting, we opened one to four 30 mm nylon mist nets (6 m and 9 m; Avinet Research Supplies, Portland, ME, USA) at dawn, and closed nets between 10:00 and 14:00, depending on ambient temperature. The site selected for netting and banding was determined with a random number generator (random.org) (accessed on 27 June 2022), however, if chemical applications were scheduled for a particular orchard block on the same day as netting, the next available site was sampled. The placement of nets within forest margins ranged from 1 m (at the edge of forest adjacent to orchard) to approximately 200 m from the forest–orchard border. Mist nets were placed in areas where birds were active and singing. During mist-netting, we broadcast species-specific playbacks from a Bluetooth speaker to lure individuals into nets (JBL Clip2; Harman International Industries, Stamford, CT, USA). Mist nets were checked every 10 min. We removed birds from the mist net, and captured individuals were transferred to paper holding bags. Each individual bird was kept for no more than 10 min. We banded birds with a United States Geological Survey (USGS) aluminum band and collected fecal samples either while handling the bird or extricated fecal material from holding bags with sterilized forceps. Fecal samples were placed in a 1.5 mL microcentrifuge tube that contained 0.5 mL RNALater solution (Thermo Fisher, Waltham, MA, USA). Samples were kept on ice until transferred to a −20 °C freezer upon return to the laboratory.

2.2. Molecular Gut Content Analysis and PCR Protocol

We used the DNeasy PowerSoil kit (Qiagen, Hilden, Germany) to extract arthropod DNA following the manufacturer’s instructions. For every 48 samples, a negative control was extracted, which did not contain avian fecal material. We included negative control extractions on plates during PCR preparation. In addition, we extracted DNA from the legs of an adult H. halys and included this extract on each plate as our positive control. We used 16S species-specific primers (16Sbr-H and 16Sar-L) to amplify H. halys present in avian fecal samples (as designed by the authors of reference [28]). PCRs were conducted at a scale of 12.5 µL containing 6.25 µL Qiagen Multiplex 2× Master mix (Qiagen, Hilden, Germany), 0.31 µL BSA, 0.625 µL of each primer (forward and reverse), 2.69 µL PCR grade H2O, and 3 µL of extracted avian fecal DNA. The thermocycling conditions for reagents were 95 °C for 15 min followed by 40 cycles of 94 °C for 45 s, 61 °C for 45 s, 72 °C for 30 s, and a final extension of 72 °C for 5 min. All PCR products were visualized on a Qiaxcel Advanced System (Qiagen, Hilden, Germany) for evaluation of positive incidence of predation on H. halys (threshold of >0.075 RFUs, [29], Supplemental Materials Table S1), in order to provide evidence of H. halys DNA in avian fecal samples.

2.3. Statistical Analysis

We tested whether the mean number of H. halys (adults and nymphs) varied according to orchard type, collection date, and year. First, we calculated the mean number of H. halys captured by site (2 traps per site) for each collection date. We fit a general linear mixed effect models in R version 4.2.2 program software (R CoreTeam 2022) using the package lme4 (function: lmer; [30]). For our model, we included orchard type (peach, pecan, and interplanted), collection date (centered and scaled), and collection year (2021 or 2022) as fixed effects, and site as a random effect. We log transformed the mean number of H. halys and used residual plots to assess model fit.

3. Results

3.1. Total H. halys and Birds Captured

A total of 5849 H. halys (adults and nymphs) were captured in pheromone-baited traps positioned in forest margins surrounding orchards during 2021–2022. Halyomorpha halys were trapped at all sites. We collected avian fecal samples from 257 individuals from 19 different bird species (Table 1). The six bird species captured most often included Carolina wren (Thryothorus ludovicianus), Eastern towhee (Pipilo erythrophthalmus), Field sparrow (Spizella pusilla), Northern cardinal (Cardinalis cardinalisis), Tufted titmouse (Baeolophus bicolor), and White-eyed vireo (Vireo griseus). The mean number of H. halys differed significantly according to collection date and year but not habitat (i.e., interplanted, peach, pecan; Figure 2). Specifically, the mean number of H. halys captured increased over the season (F1, 158 = 116.8, p < 0.0001; Figure 2) and, on average, more individuals were captured during 2021 (mean = 21.0 stink bugs per trap) than during 2022 (mean = 8.6 stink bugs per trap; F1, 166 = 8.5, p = 0.004; Figure 2).

3.2. Foraging Patterns of Birds

We detected H. halys consumption in 4 out of 257 avian fecal samples. Two Carolina wrens ate H. halys in forests surrounding peach orchards during August 2021. In interplanted peach and pecan orchards, one Tufted titmouse and one Northern cardinal ate H. halys during July 2021 and May 2022, respectively. We found no evidence of H. halys consumption by birds in forests that surround pecan orchards.

4. Discussion

For insectivorous birds, retention time of prey may occur over a short period of time, approximately 30 min to 4 h post-feeding [31,32,33]. Therefore, our results likely underestimate avian predation on H. halys based on our sample design and methodology. Nevertheless, we found three bird species consumed H. halys in forests surrounding orchards: Northern cardinal, Tufted titmouse, and Carolina wren. Both Northern cardinals and Tufted titmice are omnivorous and consume a mixed diet of seeds, berries, and insects—including stink bugs (Pentatomidae) [34,35]. Adult Northern cardinals forage on the ground as well as in shrubs and trees [36]. Adult Tufted titmice hunt for insect prey near the ground and in trees [37]. Carolina wrens are also omnivorous, but prey more so on arthropods than plant material [38]. Despite a rather small body size (approximately 20 g), analysis of Carolina wren stomach contents shows they forage on lizards, frogs, and snakes, in addition to arthropods [38]. Carolina wrens search for prey on the ground or on the trunks of trees or shrubs, and break larger prey items into smaller pieces for consumption [39]. At our study sites, all three species were common in forests near peach and pecan orchards. Furthermore, based on their foraging behavior, all three species likely encountered H. halys in forest habitats.
The size of H. halys populations in non-crop habitats fluctuates seasonally, depending on management schedules and food availability either within or surrounding orchards [6,8,9,40]. The timing of H. halys predation by Carolina wrens and Tufted titmice in peach and interplanted peach–pecan orchards occurred during late July or early August. In Georgia, this corresponds to the period of time after peach harvest, when H. halys disperse from peach orchards and into forests, that contain non-crop host plants, and likely into nearby pecan orchards as well [8]. Many host plants in forests and woodlands provide a source of food and serve as developmental hosts for H. halys [41,42,43]. Therefore, predation by these two species in forests occurred when populations in forests were high and there were few fruits available within peach orchards. The Northern cardinal consumed H. halys during the end of May in an interplanted orchard system. During this time of year, both peach and pecan fruits are developing and high numbers of H. halys were more likely to be detected within the orchards. Northern cardinals were commonly observed foraging on small insects in a variety of organic and conventionally managed row crop fields [44]. However, whether cardinals or other bird species actively forage in peach and pecan orchards is less understood. In an apple system, adult Great tits (Parus major) nested and foraged within organic apple orchards; however, pairs that nested in conventional orchards foraged in the surrounding non-crop habitat [45]. Thus, consumption of insect pests may depend on seasonal availability as well as management style.
Predation of H. halys in forests that surround orchards may occur during the time of year when adult stink bugs are overwintering. In this region, H. halys begin to overwinter in forests near peach and pecan orchards during the fall [8]. Adult H. halys emerge from overwintering sites during early spring [8]. Resident birds, such as woodpeckers and nuthatches, may glean overwintering H. halys from trees. Other birds, such as Brown thrashers (Toxostoma rufum) or Northern flickers (Colaptes auratus), may forage on H. halys from leaf litter on the ground. Thus, the present study may underestimate H. halys predation by birds because we focused our sampling efforts during the summer, when damage to peach and pecan fruits by H. halys is high [1,4]. Moreover, collection of fecal samples from additional species of birds, such as woodpeckers and nuthatches, may reveal higher incidence of H. halys predation, either during the peak summer or overwintering months.
Molecular analysis of avian diets in agroecosystems suggests that birds tend to consume more herbivores than beneficial insects [16,46,47]. In addition to H. halys, birds may contribute to the biological control of other stink bug pests such as the brown stink bug, Euschistus servus (Say) (Hemiptera: Pentatomidae), or additional insect pests that inhabit southeastern orchard agroecosystems. Two common pests found on peach trees include the lesser peach tree borer (Synanthedon pictipes) (Grote and Robinson) (Lepidoptera: Sesiidae) and the peach tree borer (Synanthedon exitiosa) (Say) (Lepidoptera: Sesiidae). Several pests damage pecan trees and nuts, including the pecan budmoth (Gretchena bolliana) (Slingerland) (Lepidoptera: Tortricidae), pecan nut casebearer (Acrobasis nuxvorella) (Neunzig) (Lepidoptera: Pyralidae), and hickory shuckworm (Cydia caryana) (Fitch) (Lepidoptera: Tortricidae). Birds may consume pecan budmoth, nut casebearer, and hickory shuckworm in pecan orchards, as many birds preferentially forage on or provision Lepidoptera to their nestlings when seasonally available [48,49,50].
The brown marmorated stink bug, H. halys, is a global pest, and due to its dispersal ability and high number of host plants, requires a multifaceted management strategy [51]. Here, we provide an initial report that birds consume H. halys in forests that surround peach and pecan orchards. In addition to birds, arthropod natural enemies, such as stink bug egg parasitoids contribute biocontrol services in habitats that surround orchards [52]. To promote natural enemies outside of forests, preserving and/or maintaining forest habitat and wildflower sources adjacent to orchards may provide refuge for both arthropod predators and parasitoids of H. halys as well as birds [53]. To promote insectivorous birds, placement of nest boxes, for species such as Western bluebirds (Sialia Mexicana), near orchards may increase insect pest control [46], or falcon nest boxes, which may reduce the presence of fruit-eating birds within orchards [54]. Future studies of bird foraging patterns in peach and pecan orchard agroecosystems should seek to identify the consumption of additional insect pests as well as H. halys.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/insects14070595/s1, Table S1: Positive consumption of H. halys by birds.

Author Contributions

Conceptualization, E.E.G., T.E.C., J.M.S., P.G.T.; data curation, E.E.G.; writing—original draft preparation, E.E.G.; writing—review and editing, E.E.G., T.E.C., J.M.S., P.G.T. All authors have read and agreed to the published version of the manuscript.

Funding

The research was funded by the United States Department of Agriculture, Agricultural Research Service, Research Project ARS 6048-22000-046-00D.

Institutional Review Board Statement

All experiments were approved by University of Georgia’s Institutional Animal Care and Use Committee (Permit No. A2021 03-0140Y1-A0). Bird banding permits and aluminum bands were issued by the Bird Banding Laboratory (USGS; Permit No. 24287) and permission granted by Georgia Department of Natural Resources to mist-net and band birds in Georgia (Scientific Collecting Permit No. 1001330062).

Data Availability Statement

The data presented in this study are available in the article.

Acknowledgments

We thank Alexis Miller and Kristie Graham (USDA-ARS) for their assistance with monitoring pheromone-baited traps and stink bug identification, Melissa Thompson (University of Georgia, Department of Entomology) for laboratory assistance, and Southern Lane Orchard Farms for allowing research on their properties.

Conflicts of Interest

The authors declare no conflict of interest. The funder had no role in the design of the study; in collection, analyses, or interpretation of the data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Leskey, T.C.; Short, B.D.; Butler, B.R.; Wright, S.E. Impact of the invasive brown marmorated stink bug, Halyomorpha halys (Stål), in Mid-Atlantic tree fruit orchards in the United States: Case studies of commercial management. Psyche J. Entomol. 2012, 2012, 535062. [Google Scholar] [CrossRef] [Green Version]
  2. Leskey, T.C.; Nielsen, A.L. Impact of the invasive brown marmorated stink bug in North America and Europe: History, Biology, Ecology, and Management. Annu. Rev. Entomol. 2018, 63, 599–618. [Google Scholar] [CrossRef] [Green Version]
  3. Rice, K.B.; Bergh, C.J.; Bergmann, E.J.; Biddinger, D.J.; Dieckhoff, C.; Dively, G.; Fraser, H.; Gariepy, T.; Hamilton, G.; Haye, T. Biology, ecology, and management of brown marmorated stink bug (Hemiptera: Pentatomidae). J. Integr. Pest Manag. 2014, 5, A1–A13. [Google Scholar] [CrossRef]
  4. Acebes-Doria, A.L.; Leskey, T.C.; Bergh, J.C. Injury to apples and peaches at harvest from feeding by Halyomorpha halys (Stål) (Hemiptera: Pentatomidae) nymphs early and late in the season. Crop Prot. 2016, 89, 58–65. [Google Scholar] [CrossRef] [Green Version]
  5. Bergh, J.C.; Morrison III, W.R.; Stallrich, J.W.; Short, B.D.; Cullum, J.P.; Leskey, T.C. Border habitat effects on captures of Halyomorpha halys (Hemiptera: Pentatomidae) in pheromone traps and fruit injury at harvest in apple and peach orchards in the Mid-Atlantic, USA. Insects 2021, 12, 419. [Google Scholar] [CrossRef] [PubMed]
  6. Blaauw, B.R.; Jones, V.P.; Nielsen, A.L. Utilizing immunomarking techniques to track Halyomorpha halys (Hemiptera: Pentatomidae) movement and distribution within a peach orchard. PeerJ 2016, 4, e1997. [Google Scholar] [CrossRef] [Green Version]
  7. Bosco, L.; Nardelli, M.; Tavella, L. First insights on early host plants and dispersal behavior of Halyomorpha halys (Hemiptera: Pentatomidae) from overwintering to crop colonization. Insects 2020, 11, 866. [Google Scholar] [CrossRef] [PubMed]
  8. Grabarczyk, E.E.; Cottrell, T.E.; Tillman, P.G. Spatiotemporal distribution of Halyomorpha halys (Stål) (Hemiptera: Pentatomidae) across a fruit and tree nut agricultural ecosystem. Environ. Entomol. 2022, 51, 824–835. [Google Scholar] [CrossRef]
  9. Hahn, N.G.; Rodriguez-Saona, C.; Hamilton, G.C. Characterizing the spatial distribution of brown marmorated stink bug, Halyomorpha halys Stål (Hemiptera: Pentatomidae), populations in peach orchards. PLoS ONE 2017, 12, e0170889. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. Garcia, K.; Olimpi, E.M.; Karp, D.S.; Gonthier, D.J. The Good, the Bad, and the Risky: Can birds be incorporated as biological control agents into integrated pest management programs? J. Integr. Pest Manag. 2020, 11, 11. [Google Scholar] [CrossRef]
  11. Maas, B.; Karp, D.S.; Bumrungsri, S.; Darras, K.; Gonthier, D.; Huang, J.C.-C.; Lindell, C.A.; Maine, J.J.; Mestre, L.; Michel, N.L. Bird and bat predation services in tropical forests and agroforestry landscapes. Biol. Rev. 2016, 91, 1081–1101. [Google Scholar] [CrossRef] [Green Version]
  12. Schmidt, J.M.; Acebes-Doria, A.; Blaauw, B.; Kheirodin, A.; Pandey, S.; Lennon, K.; Kaldor, A.D.; Toledo, P.F.; Grabarczyk, E.E. Identifying molecular-based trophic interactions as a resource for advanced integrated pest management. Insects 2021, 12, 358. [Google Scholar] [CrossRef]
  13. Mangan, A.M.; Piaggio, A.J.; Hopken, M.W.; Werner, S.J.; Pejchar, L. A molecular analysis to assess codling moth Cydia pomonella L.(Lepidoptera: Tortricidae) predation by orchard birds. Ecol. Indic. 2018, 93, 1222–1225. [Google Scholar] [CrossRef] [Green Version]
  14. Sow, A.; Seye, D.; Faye, E.; Benoit, L.; Galan, M.; Haran, J.; Brévault, T. Birds and bats contribute to natural regulation of the millet head miner in tree-crop agroforestry systems. Crop Prot. 2020, 132, 105127. [Google Scholar] [CrossRef]
  15. Crisol-Martínez, E.; Moreno-Moyano, L.T.; Wormington, K.R.; Brown, P.H.; Stanley, D. Using next-generation sequencing to contrast the diet and explore pest-reduction services of sympatric bird species in macadamia orchards in Australia. PLoS ONE 2016, 11, e0150159. [Google Scholar] [CrossRef]
  16. Garfinkel, M.; Minor, E.; Whelan, C.J. Using faecal metabarcoding to examine consumption of crop pests and beneficial arthropods in communities of generalist avian insectivores. IBIS 2022, 164, 27–43. [Google Scholar] [CrossRef]
  17. Garfinkel, M.B.; Minor, E.S.; Whelan, C.J. Birds suppress pests in corn but release them in soybean crops within a mixed prairie/agriculture system. Condor 2020, 122, duaa009. [Google Scholar] [CrossRef]
  18. Tillman, P.G.; Buntin, G.D.; Cottrell, T.E. First report of seasonal trap capture for Halyomorpha halys (Hemiptera: Pentatomidae) and native stink bugs in central Georgia. J. Entomol. Sci. 2017, 52, 455–459. [Google Scholar] [CrossRef]
  19. Khrimian, A.; Zhang, A.; Weber, D.C.; Ho, H.-Y.; Aldrich, J.R.; Vermillion, K.E.; Siegler, M.A.; Shirali, S.; Guzman, F.; Leskey, T.C. Discovery of the aggregation pheromone of the brown marmorated stink bug (Halyomorpha halys) through the creation of stereoisomeric libraries of 1-Bisabolen-3-Ols. J. Nat. Prod. 2014, 77, 1708–1717. [Google Scholar] [CrossRef]
  20. Leskey, T.C.; Agnello, A.; Bergh, J.C.; Dively, G.P.; Hamilton, G.C.; Jentsch, P.; Khrimian, A.; Krawczyk, G.; Kuhar, T.P.; Lee, D.-H. Attraction of the invasive Halyomorpha halys (Hemiptera: Pentatomidae) to traps baited with semiochemical stimuli across the United States. Environ. Entomol. 2015, 44, 746–756. [Google Scholar] [CrossRef]
  21. Weber, D.C.; Cabrera Walsh, G.; DiMeglio, A.S.; Athanas, M.M.; Leskey, T.C.; Khrimian, A. Attractiveness of harlequin bug, Murgantia histrionica, aggregation pheromone: Field response to isomers, ratios, and dose. J. Chem. Ecol. 2014, 40, 1251–1259. [Google Scholar] [CrossRef] [Green Version]
  22. Weber, D.C.; Leskey, T.C.; Walsh, G.C.; Khrimian, A. Synergy of aggregation pheromone with methyl (E, E, Z)-2, 4, 6-decatrienoate in attraction of Halyomorpha halys (Hemiptera: Pentatomidae). J. Econ. Entomol. 2014, 107, 1061–1068. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Morrison, W.R.; Lee, D.-H.; Short, B.D.; Khrimian, A.; Leskey, T.C. Establishing the behavioral basis for an attract-and-kill strategy to manage the invasive Halyomorpha halys in apple orchards. J. Pest Sci. 2016, 89, 81–96. [Google Scholar] [CrossRef]
  24. Cottrell, T.E.; Yonce, C.E.; Wood, B.W. Seasonal occurrence and vertical distribution of Euschistus servus (Say) and Euschistus tristigmus (Say)(Hemiptera: Pentatomidae) in pecan orchards. J. Entomol. Sci. 2000, 35, 421–431. [Google Scholar] [CrossRef]
  25. Cottrell, T.E. Improved trap capture of Euschistus servus and Euschistus tristigmus (Hemiptera: Pentatomidae) in pecan orchards. Fla. Entomol. 2001, 84, 731. [Google Scholar] [CrossRef]
  26. Blaauw, B.R.; Johnson, A.; Brannen, P.; Chavez, D. Southeastern Peach, Nectarine, and Plum Pest Management and Culture Guide; UGA Cooperative Extension Bulletin: Athens, GA, USA, 2023; p. 1171. [Google Scholar]
  27. Wells, L. 2023 Commercial Pecan Spray Guide; UGA Cooperative Extension Bulletin: Athens, GA, USA, 2023; p. 841. [Google Scholar]
  28. Athey, K.J.; Sitvarin, M.I.; Harwood, J.D. Laboratory and field investigation of biological control for brown marmorated stink bug (Halyomorpha halys (Stål)(Hemiptera: Pentatomidae)). J. Kans. Entomol. Soc. 2017, 90, 341–352. [Google Scholar] [CrossRef]
  29. Sint, D.; Niederklapfer, B.; Kaufmann, R.; Traugott, M. Group-specific multiplex PCR detection systems for the identification of flying insect prey. PLoS ONE 2014, 9, e115501. [Google Scholar] [CrossRef]
  30. Bates, D.; Mächler, M.; Bolker, B.; Walker, S. Fitting linear mixed-effects models using Lme4. J. Stat. Softw. 2015, 67, 48. [Google Scholar] [CrossRef]
  31. Afik, D.; Karasov, W.H. The trade-offs between digestion rate and efficiency in warblers and their ecological implications. Ecology 1995, 76, 2247–2257. [Google Scholar] [CrossRef]
  32. Levey, D.J.; Karasov, W.H. Gut passage of insects by European starlings and comparison with other species. Auk 1994, 111, 478–481. [Google Scholar] [CrossRef]
  33. Oehm, J.; Juen, A.; Nagiller, K.; Neuhauser, S.; Traugott, M. Molecular scatology: How to improve prey DNA detection success in avian faeces? Mol. Ecol. Resour. 2011, 11, 620–628. [Google Scholar] [CrossRef] [PubMed]
  34. Bent, A.C. Life Histories of North American Jays, Crows, and Titmice, Order Passeriformes; US Government Printing Office: Washington, DC, USA, 1946.
  35. McAtee, W.L. Food Habits of the Grosbeaks; US Department of Agriculture, Biological Survey: Washington, DC, USA, 1908. [Google Scholar]
  36. Dow, D.D. Habitat utilization by cardinals in central and peripheral breeding populations. Can. J. Zool. 1969, 47, 409–417. [Google Scholar] [CrossRef]
  37. Gillespie, M. Behavior and local distribution of Tufted titmice in winter and spring. Bird-Band 1930, 1, 113–127. [Google Scholar]
  38. Silver, J.; Moore, A.W.; Beal, F.E.L.; McAtee, W.L.; Kalmbach, E.R. Common Birds of the Southeastern United States in Relation to Agriculture; US Government Printing Office: Washington, DC, USA, 1941.
  39. Haggerty, T.M.; Morton, E.S. Carolina wren (Thryothorus ludovicianus). In Birds of the World; Billerman, S.M., Keeney, B.K., Rodewald, P.G., Schulenberg, T.S., Eds.; Cornell Lab of Ornithology: Ithaca, NY, USA, 2020. [Google Scholar]
  40. Maistrello, L.; Vaccari, G.; Caruso, S.; Costi, E.; Bortolini, S.; Macavei, L.; Foca, G.; Ulrici, A.; Bortolotti, P.P.; Nannini, R. Monitoring of the invasive Halyomorpha halys, a new key pest of fruit orchards in northern Italy. J. Pest Sci. 2017, 90, 1231–1244. [Google Scholar] [CrossRef]
  41. Bakken, A.J.; Schoof, S.C.; Bickerton, M.; Kamminga, K.L.; Jenrette, J.C.; Malone, S.; Abney, M.A.; Herbert, D.A.; Reisig, D.; Kuhar, T.P. Occurrence of brown marmorated stink bug (Hemiptera: Pentatomidae) on wild hosts in nonmanaged woodlands and soybean fields in North Carolina and Virginia. Environ. Entomol. 2015, 44, 1011–1021. [Google Scholar] [CrossRef] [Green Version]
  42. Bergmann, E.J.; Venugopal, P.D.; Martinson, H.M.; Raupp, M.J.; Shrewsbury, P.M. Host plant use by the invasive Halyomorpha halys (Stål) on woody ornamental trees and shrubs. PLoS ONE 2016, 11, e0149975. [Google Scholar] [CrossRef]
  43. Tillman, P.G.; Cottrell, T.E.; Grabarczyk, E.E. Black cherry as a host plant for stink bugs (Hemiptera: Pentatomidae) in agroecosystems in Georgia, USA. Fla. Entomol. 2022, 105, 79–86. [Google Scholar] [CrossRef]
  44. Jones, G.A.; Sieving, K.E.; Jacobson, S.K. Avian diversity and functional insectivory on North-Central Florida farmlands. Conserv. Biol. 2005, 19, 1234–1245. [Google Scholar] [CrossRef]
  45. Bouvier, J.-C.; Delattre, T.; Boivin, T.; Musseau, R.; Thomas, C.; Lavigne, C. Great tits nesting in apple orchards preferentially forage in organic but not conventional orchards and in hedgerows. Agric. Ecosyst. Environ. 2022, 337, 108074. [Google Scholar] [CrossRef]
  46. Jedlicka, J.A.; Vo, A.-T.E.; Almeida, R.P. Molecular scatology and high-throughput sequencing reveal predominately herbivorous insects in the diets of adult and nestling Western Bluebirds (Sialia mexicana) in California vineyards. Auk Ornithol. Adv. 2017, 134, 116–127. [Google Scholar] [CrossRef] [Green Version]
  47. Sow, A.; Haran, J.; Benoit, L.; Galan, M.; Brévault, T. DNA metabarcoding as a tool for disentangling food webs in agroecosystems. Insects 2020, 11, 294. [Google Scholar] [CrossRef] [PubMed]
  48. Burger, C.; Belskii, E.; Eeva, T.; Laaksonen, T.; Mägi, M.; Mänd, R.; Qvarnström, A.; Slagsvold, T.; Veen, T.; Visser, M.E. Climate change, breeding date and nestling diet: How temperature differentially affects seasonal changes in Pied flycatcher diet depending on habitat variation. J. Anim. Ecol. 2012, 81, 926–936. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Grabarczyk, E.E.; Gill, S.A.; Vonhof, M.J.; Alabady, M.S.; Wang, Z.; Schmidt, J.M. Diet composition and diversity does not explain fewer, smaller urban nestlings. PLoS ONE 2022, 17, e0264381. [Google Scholar] [CrossRef] [PubMed]
  50. Hajdasz, A.C.; Otter, K.A.; Baldwin, L.K.; Reudink, M.W. Caterpillar phenology predicts differences in timing of mountain chickadee breeding in urban and rural habitats. Urban Ecosyst. 2019, 22, 1113–1122. [Google Scholar] [CrossRef]
  51. Conti, E.; Avila, G.; Barratt, B.; Cingolani, F.; Colazza, S.; Guarino, S.; Hoelmer, K.; Laumann, R.A.; Maistrello, L.; Martel, G. Biological control of invasive stink bugs: Review of global state and future prospects. Entomol. Exp. Appl. 2021, 169, 28–51. [Google Scholar] [CrossRef]
  52. Tillman, G.; Toews, M.; Blaauw, B.; Sial, A.; Cottrell, T.; Talamas, E.; Buntin, D.; Joseph, S.; Balusu, R.; Fadamiro, H. Parasitism and predation of sentinel eggs of the invasive brown marmorated stink bug, Halyomorpha halys (Stål)(Hemiptera: Pentatomidae), in the Southeastern US. Biol. Control 2020, 145, 104247. [Google Scholar] [CrossRef]
  53. Tillman, G. Ecosystem-based incorporation of nectar-producing plants for stink bug parasitoids. Insects 2017, 8, 65. [Google Scholar] [CrossRef] [Green Version]
  54. Shave, M.E.; Shwiff, S.A.; Elser, J.L.; Lindell, C.A. Falcons using orchard nest boxes reduce fruit-eating bird abundances and provide economic benefits for a fruit-growing region. J. Appl. Ecol. 2018, 55, 2451–2460. [Google Scholar] [CrossRef] [Green Version]
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Figure 1. Map image showing location of study area marked with a purple square (A) in Peach County, Georgia, USA that included nine orchards (gray points) (B). At each site, two pheromone-baited traps (C) were placed in forest habitat surrounding orchards to monitor Halyomorpha halys. Birds were captured in mist nets and fecal samples collected in forest margins surrounding the orchards (turquoise points).
Figure 1. Map image showing location of study area marked with a purple square (A) in Peach County, Georgia, USA that included nine orchards (gray points) (B). At each site, two pheromone-baited traps (C) were placed in forest habitat surrounding orchards to monitor Halyomorpha halys. Birds were captured in mist nets and fecal samples collected in forest margins surrounding the orchards (turquoise points).
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Figure 2. Mean number of H. halys captured in pheromone-baited traps by habitat in forests surrounding commercial orchards in Peach County, Georgia, USA during the years (A) 2021 and (B) 2022. A regression line (Loess) and 95% confidence intervals are displayed for weekly means by habitat (points).
Figure 2. Mean number of H. halys captured in pheromone-baited traps by habitat in forests surrounding commercial orchards in Peach County, Georgia, USA during the years (A) 2021 and (B) 2022. A regression line (Loess) and 95% confidence intervals are displayed for weekly means by habitat (points).
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Table
Table 1. Summary of bird species and total number of avian fecal samples for each species collected during 2021 and 2022 in peach and pecan orchards in Peach County, Georgia, USA.
Table 1. Summary of bird species and total number of avian fecal samples for each species collected during 2021 and 2022 in peach and pecan orchards in Peach County, Georgia, USA.
Common NameScientific Name20212022Total
Blue-gray gnatcatcherPolioptila caerulea101
Blue JayCyanocitta cristata101
Brown ThrasherToxostoma rufum011
Carolina ChickadeePoecile carolinensis415
Carolina WrenThryothorus ludovicianus642084
Eastern KingbirdTyrannus tyrannus101
Eastern TowheePipilo erythrophthalmus21526
Eastern Wood PeweeContopus virens404
Field SparrowSpizella pusilla24832
Great Crested FlycatcherMyiarchus crinitus426
Gray CatbirdDumetella carolinensis011
Indigo BuntingPasserina cyanea415
Northern CardinalCardinalis cardinalis30737
Northern MockingbirdMimus polyglottos101
Pine WarblerSetophaga pinus099
Summer TanagerPiranga rubra145
Tufted TitmouseBaeolophus bicolor13619
White-eyed VireoVireo griseus11718
Wood ThrushHylocichla mustelina101
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MDPI and ACS Style

Grabarczyk, E.E.; Cottrell, T.E.; Schmidt, J.M.; Tillman, P.G. Low Incidence of Avian Predation on the Brown Marmorated Stink Bug, Halyomorpha halys (Hemiptera: Pentatomidae), in Southeastern Orchard Systems. Insects 2023, 14, 595. https://doi.org/10.3390/insects14070595

AMA Style

Grabarczyk EE, Cottrell TE, Schmidt JM, Tillman PG. Low Incidence of Avian Predation on the Brown Marmorated Stink Bug, Halyomorpha halys (Hemiptera: Pentatomidae), in Southeastern Orchard Systems. Insects. 2023; 14(7):595. https://doi.org/10.3390/insects14070595

Chicago/Turabian Style

Grabarczyk, Erin E., Ted E. Cottrell, Jason M. Schmidt, and P. Glynn Tillman. 2023. "Low Incidence of Avian Predation on the Brown Marmorated Stink Bug, Halyomorpha halys (Hemiptera: Pentatomidae), in Southeastern Orchard Systems" Insects 14, no. 7: 595. https://doi.org/10.3390/insects14070595

APA Style

Grabarczyk, E. E., Cottrell, T. E., Schmidt, J. M., & Tillman, P. G. (2023). Low Incidence of Avian Predation on the Brown Marmorated Stink Bug, Halyomorpha halys (Hemiptera: Pentatomidae), in Southeastern Orchard Systems. Insects, 14(7), 595. https://doi.org/10.3390/insects14070595

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