Krome Memorial Section

Proc. Fla. State Hort. Soc. 128:55–57. 2015.

Cold Tolerance and Distribution of Myllocerus undecimpustulatus undatus (Coleoptera: ) (Sri Lankan Weevil) in Florida

Anita S. Neal*1, Ronald D. Cave2, and Rodrigo Diaz3 1University of Florida, IFAS, St. Lucie County Extension, 8400 Picos Rd, Ft. Pierce, FL 34945 2University of Florida, IFAS, Indian River Research and Education Center, 2199 South Rock Rd, Ft. Pierce, FL 34945 3Lousiana State University, 156 Thomas Boyd Hall, Baton Rouge, LA 70803

Additional index words. species distribution models, repeated cold exposure, sustained cold exposure Myllocerus undecimpustulatus undatus Marshall, the Sri Lankan weevil, is a serious plant pest with a wide range of hosts. It was first identified in the United States on Citrus sp. in Davie, Broward County, Florida, on 15 September 2000. This weevil has over 150 different host plant species including fruits, nuts, vegetables, and ornamentals. It has been detected in 26 counties in Florida through December 2012. Historical data from 2000–15 obtained from the Division of Plant Industry’s field agent submissions indicate the northward spread of the Sri Lankan weevil in North America. Cold tolerance data indicate adults are acclimated to lower temperatures until reaching 0 °C and –5 °C. A sustained and multiple exposure experiment that more closely resembles actual cold events in Florida and other potential areas tested gathered in summer and winter to determine increased cold hardiness. This may provide valuable information to assist Extension agents and pest management professionals in preparing control strategies.

Insects are more likely to be susceptible to climate modifica- al 2009). Ten were selected from a region in southern tions because their basic physiological functions are strongly South America along with six predictor variables extracted from influenced by environmental factors (Deutsch et al. 2007). The WorldClim and Climate Research Unit databases and tested with most significant factors in the environment influencing eight of the most commonly used SDMs (Tognelli et al 2009). The function are temperature and humidity (Singh et al. 2009). Specific differences of projections between SDMs were recognized and strategies to overcome stressful environments include behavioral suggested that these models are simply a hypothesis of possible avoidance, migration, diapause, and adaptation (Bale and Hayward distributions of a species (Tognelli et al 2009). 2009). Adaptation of an organism to changing environmental Laboratory or field cold tolerant experiments may improve the conditions may happen in its lifetime, or through many genera- projections of a SDM. A study with Microtheca ochroloma Stål tions as an evolutionary adaptation (Singh et al 2009). The ability at cold temperatures of 5, 0, and –5 °C, found the egg stage was of an insect to develop at different temperatures is an important the most cold tolerant, and the first instar the least (Manrique et adaption to survive in different climatic conditions, which is valu- al 2012). This experiment acclimated individuals gradually to able in predicting insect outbreaks (Mizell and Nebeker 1978). cooler temperatures from 15°C to the final temperature by 5 °C Over time, insects that are subjected to cooler temperatures may intervals each day. The times required to kill 50 (LT50) and 90% evolve morphological, physiological, and behavioral adaptions (LT90) of the population were estimated, models were developed, (Lalouette et al. 2009). These adaptions may possibly enable maps imported to ArcGis and isothermal lines created predicting them to move into other regions. areas favorable for Microtheca ochroloma. Stratman et al. (2014) Insects have the potential to become invasive in regions where predicted the potential distribution of the biological control agent, they were previously unknown, and where temperature can have Cricopus lebetis Sublette, a tip miner of the invasive aquatic plant, a direct impact on the probability of establishment (Bale and Hydrilla verticillata (L. f.) Royle, utilizing predictions from cold Hayward 2009). Species distribution models (SDMs) utilize geo- tolerance data and ecological niche testing. graphic information systems (GIS), along with computer software Cold tolerant studies are usually focused on the effects of a packages and climate databases, to predict a particular species single cold exposure on insects under laboratory conditions. A distribution (Elith and Leathwick 2009, Franklin 2009, Stratman rapid cold-hardening study subjected over-wintering pine needle et al. 2014). These models allow us to project the geographic gall midge larvae, Thecodiplosis japonesis Uch. et Inouye, to distribution of adventive species into other regions (Tognelli et 4 °C for two hours, then back to 27 °C for 15, 30, or 60 minutes prior to transferring to –15°C for three hours (Yi-ping et al. 2000). A non-conditioned group was held at 27 °C for 15, 30, and 60 minutes prior to transferring to –15 °C for three hours *Corresponding author. Email: [email protected]. (Yi-ping et al. 2000). The survival rate of conditioned larvae was

Proc. Fla. State Hort. Soc. 128: 2015. 55 Fig. 1. The spread of Sri Lankan weevils, Myllocerus undecimpustulatus undatus Marshall, in Florida based on Division of Plant Industry collections from 2000 to 2015. Credits: Anita Neal, UF/IFAS and diymaps.net

40.0% and unconditioned larvae 17.9%, suggesting that rapid the larvae injure roots (O’Brien et al. 2006). Arevalo and Stansly cold-hardening is effective at increasing larval survival (Yi-ping (2009) found heavy infestations of Sri Lankan weevil in citrus et al. 2000). Marshall and Sinclair (2012) looked at repeated groves, and recent reports confirm damage to other economically cold exposures (RCE) with Drosophilia melanogaster Meigen important crops, such as avocado, peaches and lychee (R. Banack crossing the chill-coma threshold at or below 10 °C in which all and M. Luciano, personal communication, Apr. 2015). muscular movement ceases (MacMillan and Sinclair 2010). The When adult weevils feed on leaves, they feed inward from control group was maintained at a relatively warm temperature, the leaf margins (or edges), causing typical leaf notching. There the RCE groups experienced repeated short cold exposures and are some instances where the leaf material is almost completely the sustained cold exposure group was exposed once, for a long defoliated, when the weevil has fed along the leaf veins. The adults period (Marshall and Sinclair 2012). The authors found that RCE prefer new plant growth. Intense feeding by numerous weevils were perceived as advantageous to immediate survival, along with may cause plant decline or stunting. Young seedlings may not increasing cold hardiness when compared to insects experiencing survive a large amount of feeding damage. With healthy plants, a single, prolonged cold exposure (Marshall and Sinclair 2012). however, the feeding damage may be considered cosmetic if the However, few studies have focused on the potential distribution plant recovers. Larvae feed on plant roots for approximately one of tropical adventive pest species found in different climates. to two months. This tropical insect is native to a climate where Myllocerus undecimpustulatus undatus Marshall (Coleoptera: the coldest temperature is 22 °C. Curculionidae) is a polyphagous broad-nosed weevil with a wide A cold tolerance study was developed to define range expan- range of hosts (Neal 2013). M. undecimpustulatus undatus, a sion. Weevil locations were assigned geographical coordinates native of Sri Lanka, is a subspecies of the widely distributed M. and entered into DIVA-GIS software and mapped. The model undecimpustulatus (O’Brien et al. 2006). M. undecimpustulatus projected potential spread throughout the southern United States. undatus, the Sri Lankan weevil, originated in Asia but has estab- A cold tolerant study with adult weevils, similar to the experi- lished populations in Florida. M. undecimpustulatus undatus was mental design of Manrique et al. (2012), established that they first identified in Florida in 2000. By 2015, the Florida Division could survive at –5 °C for five days. Another experiment was of Plant Industry (DPI) identified the weevil as being present in designed similar to Marshall and Sinclair (2012) implementing 27 Florida counties and infesting over 150 different plant species RCE that more closely resemble actual cold events in Florida and (Fig. 1). Submissions from DPI field agents were identified by other potential areas. The RCE had minimal effect on mortality Michael Thomas, starting with the first identified occurrence in and feeding of adult weevils, whereas the weevils subjected to Sept. 2000 and continuing through Dec. 2012. Adults are foli- sustained cold exposure suffered a greater mortality rate and vores of ornamental plants, fruit trees, and vegetables, whereas consumed less food. This sustained exposure not only affects

56 Proc. Fla. State Hort. Soc. 128: 2015. their feeding, but may have other negative impacts on fecundity ochroloma (Coleoptera: Chrysomelidae), a pest of cruciferous crops in and longevity. the southeastern United States. Ann. Entomol. Soc. Amer. 105:859–864. M. undecimpustulatus undatus has the potential to make Marshall, K.E., and B.J. Sinclair. 2010. Repeated stress exposure results adaptions which will allow it to move into other areas with the in survival-reproduction trade-off in Drosophilia melanogaster. Proc. southern United States. The most likely route would be through Biol. Sci. 277:963–969. movement of potted plant material. This insect has shown the Marshall, K.E., and B.J. Sinclair. 2012. The impacts of repeated cold ability to survive for five days at –5 °C and has demonstrated exposure on insects. The J. Exp. Bio. 215:1607–1613. though repeated cold exposures that it has the ability to adapt Mizell, R.F. and T.E. Nebeker. 1978. Estimating the developmental and survive. time of the southern pie Dendroctonus frontalis as a function of field temperature. Environ. Entomolo. 7:592–595. Neal, A. 2013. Sri Lankan weevil, Myllocerus undecimpustulatus un- Literature Cited datus Marshall (Coleoptera: Cuculionidae, ). University of Florida/IFAS extension. Publication number: EENY-579 . Accessed 5 May 2015. (Coleoptera: Curculionidae) in Valencia Orange with chlorpyrifos spray O’Brien, C.W., M. Haseeb, and M.C. Thomas. 2006. Myllocerus undec- directed at ground and foliage. Fla. Entomol. 92:150–152. impustulatus undatus Marshall (Coleoptera: Curculionidae), A recent Bale, J.S. and S.A.L. Hayward. 2009. Insect overwintering in a chang- discovered pest weevil from the Indian subcontinent. Florida Dept. of ing climate. J. Exp. Biol. 213:980–994. Agr. and Cons. Serv., Entomology Circular No. 412. Deutsch, C.A., J.J. Tewksbury, R.B. Huey, K.S. Sheldon, C.K. Ghalam- Singh, T., M.M. Bhat, and M.A. Khan. 2009. Insect adaptions to bor, D.C. Haak, and P.R. Martin. 2008. Impacts of climate warming changing environments—temperature and humidity. Int. J. Indust. on terrestrial ectotherms across latitude. PNAS. 105:6668–6672. Entomol. 19:155–164. Elith, J., and J.R. Leathwick. 2009. Species distribution models: Eco- Stratman, K.N., W.A. Overholt, J.P. Cuda, A. Mukherjee, R. Diaz, logical explanation and prediction across space and time. Ann. Rev. M.D. Netherland, and P.C. Wilson. 2014. Temperature-dependent Evol. Syst. 40:677–697. development, cold tolerance, and potential distribution of Cricotopus Laloutte, L., C.M. Williams, F. Hervant, B.J. Sinclair, and D. Renault. lebetis (Diptera: Chironomidae), a tip miner of Hydrilla verticillata 2011. Metabolic rate and oxidative stress in insects exposed to low (Hydrocharitaceae). J. Insect Sci. 14:1–8. temperature thermal fluctuations. Comp Biochem. Physio. A. Mol. Tognelli, M.F., S.A. Roig-Juñent, A.E. Marvaldi, G.E. Flores, and J.M. Integr. Physiol. 158:229–234. Lobo. 2009. An evaluation of methods for modelling distribution of MacMillian, H.A., and B.J. Sinclair. 2011. Mechanisms underlying Patagonian insects. Rev. Chil. Hist. Nat. 82:347–360. insect chill-coma. J. Insect Physiol. 57:12–20. Yi-ping, L., G. He, H-Y. Park, and M. Goto. 2001. Rapid cold hardening Manrique, V.R. Diaz, C. Montemayor, D. Serrano, and R.D. Cave. 2012. providing higher cold tolerance than cold acclimation in the pine needle Temperature-dependent development and cold tolerance of Microtheca gall midge Thecodiplosis japonensis larvae. Entomol. Sinica. 8:81–88.

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