Translator Disclaimer
30 September 2019 Feeding Responses of Euthyrhinchus floridanus (Hemiptera: Pentatomidae) to Brown Marmorated Stinkbug (Hemiptera: Pentatomidae) Adults and Nymphs
Author Affiliations +

The Florida predatory stink bug, Euthyrhynchus floridanus L. (Hemiptera: Pentatomidae), is a generalist predator native to North America that feeds on a broad range of lepidopterous and heteropterous key pests in a great diversity of crops and non-crop situations. Feeding tests conducted in the laboratory to determine the most susceptible stage of the brown marmorated stink bug, Halyomorpha halys (Stål) (Hemiptera: Pentatomidae), to third nymphal instar, and male and female E. floridanus, indicated that this predator has great potential for biological control of H. halys nymphs and adult stages.

Euthyrhynchus floridanus (L.) (Hemiptera: Pentatomidae), is a native predator that is common throughout the yr in many agro-ecosystems. It preys on a diversity of crop pests, including immature beetles, lepidopterous pests, and true bugs including plant-damaging pentatomoids (Mead 1976; Logan et al. 1987; Medal et al. 2018). The distribution range includes the central and southeastern USA, Mexico, Central, and South America into southern Brazil (Ables 1975; Mead & Richman 2013). Adults and nymphs tend to be aggregated and have a low level of cannibalism (Medal personal observation). Both nymphs and adults capture prey of different sizes, and feed individually or in aggregations. Since the discovery of the brown marmorated stink bug in Pennsylvania in 1996 (Hoebeke & Carter 2003), attempts have been made to use parasitoids and predators (Dieckhoff & Hoelmer 2014; Lara et al. 2016) as a sustainable management option of this new invasive polyphagous Asian immigrant (Hamilton et al. 2008; Haye et al. 2015; Leskey & Nielsen 2018) that has been reported in 44 states, including a limited reproductive localized infestation in Lake County, Florida (Northeastern IPM Center 2017; Penca & Hodges 2018). In this laboratory study, we determined the feeding response of E. floridanus to brown marmorated stinkbug Halyomorpha halys (Stål) (Hemiptera: Pentatomidae) nymphs and adults in controlled environmental conditions.

Euthyrhynchus floridanus used in this study was obtained from a laboratory colony established from nymphs and adults collected in a kudzu (Pueraria montana Lour (err.) variety lobata (Willd.); Fabaceae) patch in Gainesville, Alachua County, Florida, USA (29.639686°N, 82.399092°W) during the summer-fall of 2014. The second to fifth instars and adult brown marmorated stinkbug used in the experiments were obtained from a colony obtained from the USDA-ARS laboratory colony located in Newark, New Jersey, USA, and held in the laboratory in clear plastic containers (23 cm width × 32 cm length × 10 cm height) with moistened paper, and bean pods and carrots. Growing conditions were set at 25 ± 3 °C, 16:8 h (L:D) photoperiod, and 50 to 60% RH.

Euthyrhynchus floridanus nymphs, and male and female adults were starved for 24 h before the experiment. Predators were placed individually in Petri dishes (14.6 cm × 2.5 cm) with a bean pod, Phaseolus vulgaris L. (Fabaceae), and moistened paper as food and moisture sources. Crumpled Kimwipes® (Kimberly-Clark, Roswell, Georgia, USA) were inserted in each dish to provide refugia for predators. One brown marmorated stinkbug nymphal instar or an adult was provided to 1 E. floridanus third nymphal instar, or a male or female adult predator. Control consisted of the same experimental set-up with only prey. The predator-prey studies incorporated a completely randomized design with 20 replications for predator prey interaction. After 24 h, the number of dead prey was recorded. Percent prey mortality data for each predator stage was analyzed using Fisher's Exact Test for Count Data (Fisher 1970). Mean prey mortality resulting from predation on developmental stage was analyzed as a 2-way factorial and compared using Tukey's multiple comparison test of means (Montgomery 2013). Means were considered statistically different at P < 0.05). Brown marmorated stinkbug mortality data were not adjusted because of low (< 5%) mortality in controls. These studies were conducted during 2015 and 2016. Predation rate of E. floridanus to brown marmorated stinkbug has not been reported previously in the literature.

These studies indicated that the feeding responses of E. floridanus male, female, and third nymphal instar to brown marmorated stinkbug generally were affected by the prey developmental stage (Tables 1 & 2). The percent mortality of brown marmorated stinkbug adults or nymphs due to E. floridanus male, female, or intermediate nymph differed significantly (X2 = 25; df = 7; P = 0.036584738). Females had a preference to feed on brown marmorated stinkbug second to fourth nymphal instar, whereas males did not show any difference in the feeding response to the brown marmorated stinkbug nymphal instar (Table 1). The E. floridanus female was more effective than males, showing higher prey mortality of brown marmorated stinkbug male or female (df = 3; P = 0.021). The feeding responses (30–40%) by E. floridanus third nymphal instar to brown marmorated stinkbug second to fourth nymphal instars were significantly different (df = 3; P < 0.05) than those obtained on the fifth nymphal instar (Table 2). Mortality of brown marmorated stinkbug nymphs ranged from 30 to 100% for E. floridanus females, and from 50 to 70% for E. floridanus males. Euthyrhynchus floridanus males were not able to feed on brown marmorated stinkbug females, probably due to the larger size of the female prey than the male predator. This was contrary to the female predators, which fed an average of 80% on female prey (Table 1). A possible explanation for the lower feeding response, in addition to the difference in size, may be related to the defense mechanism of larger prey sizes when attacked by a predator. Results indicated that E. floridanus, as an effective predator of the brown marmorated stinkbug, may complement other control strategies to reduce its population in infested regions.

Table 1.

Mortality (% ± SD) of brown marmorated stinkbug, Halyomorpha halys caused by Euthyrhynchus floridanus male and female.


The authors thank J. Howard Frank (University of Florida) and Phillip Lake (Florida Department of Agriculture and Consumer Services) for reviewing the manuscript. We also thank the staff of FDACS-Division of Plant Industry's Biological Control Rearing Facility for providing the Lepidoptera caterpillars used to feed the predator colony. This research was partially funded by the USDA-APHIS-PPQ, FDACS-DPI, and Universidad Autónoma Chapingo, Mexico.

Table 2.

Mortality (% ± SD) of brown marmorated stinkbug, Halyomorpha halys nymphs caused by Euthyrhynchus floridanus third instar.


References Cited


Ables JR. 1975. Notes on the biology of the predaceous pentatomid Euthyrhynchus floridanus (L.). Journal of the Georgia Entomological Society 10: 353–356. Google Scholar


Dieckhoff C, Hoelmer KA. 2014. Classic biological control: status of host-range tests with Asian egg parasitoids. Northeastern IPM Center. accessed 18 May 2019). Google Scholar


Fisher RA. 1970. Statistical Methods for Research Workers. Oliver & Boyd, London, United Kingdom. Google Scholar


Hamilton GC, Shearer PW, Nielsen AL. 2008. Brown marmorated stink bug – a non-native insect in New Jersey. Fact Sheet FS002. Rutgers NJAES Cooperative Extension. Rutgers University, New Brunswick, New Jersey, USA. Google Scholar


Haye T, Gariepy T, Hoelmer K, Rossi JP, Streito JC, Tassus X, Desneuz N. 2015. Range expansion of the invasive brown marmorated stinkbug, Halyomorpha halys: an increasing threat to field, fruit, and vegetable crops worldwide. Journal of Pest Science 88: 665–673. Google Scholar


Hoebeke ER, Carter ME. 2003. Halyomorpha halys Stål (Hemiptera: Pentatomidae): a polyphagous plant pest from Asia newly detected in North America. Proceedings of the Entomological Society of Washington 105: 225–237. Google Scholar


Lara J, Pickett C, Ingels C, Haviland DR, Grafton-Cardwell E, Doll D, Bethke J, Faber B, Dara SK, Hoddle M. 2016. Biological control program is being developed for brown marmorated stink bug. California Agriculture 70: 15–23. Google Scholar


Leskey TC, Nielsen AL. 2018. Impact of the invasive brown marmorated stink bug in North America and Europe: history, biology, ecology, and management. Annual Review Entomology 63: 433–452. Google Scholar


Logan PA, Casagrande RA, Hsiao TH, Drummond FA. 1987. Collection of natural enemies of Leptinotarsa decemlineata (Coleoptera: Chrysomelidae) in Mexico. Entomophaga 32: 249–254. Google Scholar


Mead FW, Richman DB. 2013. Florida predatory stinkbug, Euthyrhynchus floridanus (Linnaeus) (Insecta: Hemiptera: Pentatomidae). UF/IFAS, FDACS, DPI Publication EENY-157. University of Florida, Gainesville, Florida, USA. accessed 18 May 2019). Google Scholar


Medal J, Srivastava M, Sharma S, Wolaver D, Santa Cruz A, Rohrig E, Howe A. 2018. Laboratory feeding responses of Euthyrhynchus floridanus and Podisus maculiventris (Hemiptera: Pentatomidae) to the kudzu bug, Megacopta cribraria (Hemiptera: Plataspidae). Florida Entomologist 101: 382–388. Google Scholar


Montgomery DC. 2013. Design and Analysis of Experiments. John Wiley & Sons, Inc., Hoboken, New Jersey, USA. Google Scholar


Northeastern IPM Center. 2017. . Cornell University, Ithaca, New York, USA. Google Scholar


Penca C, Hodges A. 2018. First report of brown marmorated stink bug (Hemiptera: Pentatomidae) reproduction and localized establishment in Florida. Florida Entomologist 101: 708–711. Google Scholar
Rubí Arellano, Julio Medal, Gregorio Arellano, and Juan Pérez "Feeding Responses of Euthyrhinchus floridanus (Hemiptera: Pentatomidae) to Brown Marmorated Stinkbug (Hemiptera: Pentatomidae) Adults and Nymphs," Florida Entomologist 102(3), 658-659, (30 September 2019).
Published: 30 September 2019

Back to Top