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Predation on the Scorpion Centruroides hentzi (Banks) (Scorpiones: Buthidae) by the Assassin Bug Microtomus purcis (Drury) (Insecta: Hemiptera: Reduviidae)
Dirk J. Stevenson and Kevin M. Stohlgren

Southeastern Naturalist, Volume 14, Issue 1 (2015): N1–N4

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N1 2015 Southeastern Naturalist Notes Vol. 14, No.1 D.J. Stevenson and K.M. Stohlgren Predation on the Scorpion Centruroides hentzi (Banks) (Scorpiones: Buthidae) by the Assassin Bug Microtomus purcis (Drury) (Insecta: Hemiptera: Reduviidae) Dirk J. Stevenson1,* and Kevin M. Stohlgren1 Abstract - The diverse assemblage of invertebrates associated with Pinus (pine) snags in Florida and the Coastal Plain of Georgia include the large, widely distributed assassin bug, Microtomus purcis, and the scorpion Centruroides hentzi which is restricted to this region. We describe two instances of predation by M. purcis on C. hentzi in Georgia. These represent the first documented observations of predation on a scorpion species by an assassin bug. Documented invertebrate predators of scorpions include other arachnids (spiders, solifugids), and other scorpions, centipedes, and some insects, including ants (McCormick and Polis 1990). Although a diverse assemblage of invertebrates including cockroaches, jumping 1The Orianne Society, 100 Phoenix Road, Athens, GA 30605. *Corresponding author - dstevenson@ Manuscript Editor: Jason M. Cryan Notes of the Southeastern Naturalist, Issue 14/1, 2015 Figure 1. The assassin bug, Microtomus purcis, preying on the scorpion, Centruroides hentzi (Cumberland Island, Camden County, GA). 2015 Southeastern Naturalist Notes Vol. 14, No. 1 N2 D.J. Stevenson and K.M. Stohlgren spiders, beetles, centipedes, a scorpion, and hemipterans are common on Pinus (pine) snags in Coastal Plain habitats of the southeastern US, little has been published regarding their predator–prey interactions (Folkerts et al. 1993, Hwang and Weirauch 2012). Herein, we detail two instances of predation by the bark-dwelling assassin bug Microtomus purcis (Drury) (Hemiptera: Reduviidae) on the scorpion Centruroides hentzi (Banks) (Scorpiones: Buthidae), representing the first reported instances of predation on scorpions by an assassin bug. On 27 October 2012 at 1330 hours, we observed an adult M. purcis (~25.0 mm in length) preying on a subadult (~30 mm in total length) C. hentzi under the exfoliating bark of a large pine snag in open pine-flatwoods habitat on Cumberland Island, Camden County, GA (Fig. 1). The assassin bug was oriented vertically on the bole of the snag, 1.5 m above the ground, with its head and body facing downward; the rostrum of the assassin bug was inserted into the posterior portion of the mesosoma of the limp and presumably dead scorpion. On 2 April 2014 at 0935 hours, we observed an adult M. purcis (27.0 mm in length) preying on an adult male C. hentzi (46.4 mm in total length) beneath the bark of a Pinus palustris Miller (Longleaf Pine) snag. The assassin bug was 1.5 m above the ground, oriented vertically, and was holding the mouthparts of the limp and presumably dead C. hentzi. When disturbed by our presence, the assassin bug released the scorpion and both animals fell to the ground. An obvious injury to the tibia of the left pedipalp of the scorpion was evident when they were photographed 5 minutes later (Fig. 2). This observation occurred in firemanaged, mesic Longleaf Pine–Aristida stricta Michaux (Wiregrass) flatwoods habitat on Fort Stewart in Liberty County, GA. Figure 2. An adult assassin bug (Microtomus purcis) photographed next to the adult male scorpion (Centruroides hentzi) it had just killed and was consuming when discovered by the authors (Fort Stewart, Liberty County, GA). N3 2015 Southeastern Naturalist Notes Vol. 14, No.1 D.J. Stevenson and K.M. Stohlgren Centruroides hentzi occurs throughout much of the lower and middle Coastal Plain of Georgia and throughout most of Florida (Shelley and Sissom 1994, Stevenson et al. 2012) and is closely associated with pine bark; scorpions of all life stages are often abundant under the exfoliating bark of pine snags (Stevenson et al. 2012). Other documented predators of C. hentzi include the introduced Osteopilus septentrionalis Duméril & Bibron (Cuban Treefrog) and Leuconotopicus borealis del Hoyo and Collar (Red-cockaded Woodpecker) (Granatosky et al. 2011, Hanula and Engstrom 2000). Assassin bugs (Hemiptera: Reduviidae) are the largest clade of predatory non-holometabolous insects (~6800 described species), and one of the largest clades of predatory animals (Hwang and Weirauch 2012). Some species possess salivary venoms which aid in prey capture and digestion (Sahayaraj and Muthukumar 2011). Like many other assassin bug species, the rostrum of M. purcis may deliver a painful bite to humans (D.J. Stevenson and K.M. Stohlgren, pers. observ.). Additionally, disturbed specimens of M. purcis typically release a strong and pungent secretion. M. purcis is wide-ranging, occurring throughout much of the southeastern US from Florida to Maryland and West Virginia, and as far west as Missouri and Texas (Swanson 2011). Throughout its range, M. purcis is a bark-dwelling species associated with coarse woody debris such as snags and logs. It is a generalist predator of small invertebrates, including roaches (Horn and Hanula 2002). Field observations in southern Georgia indicate that adults and early instars are commonly found beneath the bark of pine snags (D.J. Stevenson and K.M. Stohlgren, unpubl. data). Considering that both M. purcis and C. hentzi are characteristically associated with pine snags in Coastal Plain habitats in Georgia and Florida, we suspect that predator–prey interactions between these species are frequent. It is certainly possible that early instars of M. purcis are preyed upon by larger specimens of C. hentzi. Acknowledgments. The authors thank David Sissom for his help with this note. Literature Cited Folkerts, G.W., M.A. Deyrup, and D.C. Sisson. 1993. Arthropods associated with xeric Longleaf Pine habitats in the southeastern United States: A brief overview. Pp. 159–192, In S.M. Hermann (Ed.). Proceedings of the 18th Tall Timbers Fire Ecology Conference, The Longleaf Pine Ecosystem: Ecology, Restoration, and Management. Tall Timbers Research, Inc., Tallahassee, FL. 418 pp. Granatosky, M.C., L.M. Wagner, and K.L. Krysko. 2011. Natural history note—Osteopilus septentrionalis (Cuban Treefrog): Prey. Herpetological Review 42:90. Hanula, J.L., and R.T. Engstrom. 2000. Comparison of Red-cockaded Woodpecker (Picoides borealis) nestling diet in old-growth and old-field Longleaf Pine (Pinus palustris) habitats. American Midland Naturalist 144:370–376. Horn, S., and J.L. Hanula. 2002. Life history and habitat associations of the Broad Wood Cockroach, Parcoblatta lata (Blattaria: Blattellidae), and other native cockroaches in the coastal plain of South Carolina. Annals of the Entomological Society of America 95(6):665–671. Hwang, W.S., and C. Weirauch. 2012. Evolutionary history of assassin bugs (Insecta: Hemiptera: Reduviidae): Insights from divergence dating and ancestral state reconstruction. PLoS ONE 7(9): e45523. doi:10.1371/journal.pone. McCormick, S.J., and G.A. Polis. 1990. Prey, predators, and parasites. Pp. 294–320, In G.A. Polis (Ed.). The Biology of Scorpions. Stanford University Press, Stanford, CA. 587 pp. Sahayaraj, K., and S. Muthukumar. 2011. Zootoxic effects of reduviid Rhynocoris marginatus (Fab.) (Hemiptera: Reduviidae) venomous saliva on Spodoptera litura (Fab.) Toxicon 58(5):415–425. Shelley, R.M., and W.D. Sissom. 1994. Distributions of the scorpions Centruroides vittatus (Say) and Centruroides hentzi (Banks) in the United States and Mexico (Scorpiones, Buthidae). Journal of Arachnology 23:100–110. 2015 Southeastern Naturalist Notes Vol. 14, No. 1 N4 D.J. Stevenson and K.M. Stohlgren Stevenson, D.J., G. Greer, and M.J. Elliott. 2012. The distribution and habitat of Centruroides hentzi (Banks) (Scorpiones, Buthidae) in Georgia. Southeastern Naturalist 11(4):589–598. Swanson, D.R. 2011. New state records and distributional notes for some assassin bugs of the continental United States. The Great Lakes Entomologist 44(3-4):117–138.