The feeding responses of the predatory stink bugs E. floridanus and P. maculiventris to the citrus root weevil D. abbreviatus were studied at the Florida Department of Agriculture and Consumer Services, Division of Plant Industry's Florida Biological Control Laboratory in Gainesville, FL. This work was done in quarantine at temperatures of 25° ± 3 °C with a 16-hour photoperiod (16:8 L/D) and a relative humidity of 50–55%. The E. floridanus and P. maculiventris males, females and 3rd–5th instars were kept individually in a Petri dish with a bean pod and moistened paper for 24 h. They were then exposed to a single D. abbreviatus male or female in Petri-dishes for 24 h. Twenty replications were made. At the end of the experiment percent predation was determined. Euthyrhynchus floridanus was more efficient than P. maculiventris at feeding on D. abbreviatus adults in the lab with no choice tests. This particular stinkbug can be easily mass reared and therefore has potential as augmentative biological control agent for the citrus root weevil. However, more testing is necessary to determine the overall impact of this predator in the field.
Diaprepes root weevil or citrus weevil, Diaprepes abbreviatus (L.) (Coleoptera: Curculionidae), a native of the Caribbean (Martorell 1976; Wolcott & French 1936), is an important pest of citrus, sugarcane, ornamentals and other crops in Florida (Peña & Amalin 2011). It was first reported in Florida in 1964 in Orange County (Woodruff 1968), and since has spread throughout southern and central Florida. It is estimated that citrus root weevil is responsible for more than US$ 70 million in damage to at least 40,000 ha of citrus groves in Florida (Weissling et al. 2012). This weevil is relatively large with adults ranging from 10 to 20 mm in length. There are several morphotypes with yellow or orange stripes on a black background on the elytra. In 2000, the citrus root weevil was found in a citrus grove in the Rio Grande Valley of Texas (Skaria & French 2001), where it quickly became established. This insect was first found in Orange and Los Angeles counties, California in 2005 and in fall 2006 in San Diego County. Efforts to eradicate the citrus weevil in California were unsuccessful and it is currently established in several counties presenting a high risk of spreading further (Jetter & Godfrey 2009). In its native range in the Caribbean islands, it is one of the most important crop pests, feeding on many hosts (more than 290 plant species in 59 families) including citrus, legumes, vegetables, corn, sorghum and several weeds (Simpson et al. 1996). The most significant damage is caused by the larvae feeding on the roots of host plants. Females have a great reproductive potential laying an average of 5,000 eggs during a lifetime of approximately 5 months (Wolcott & French 1936). Females lay a cluster of 30 to 264 eggs on the leaves. Larvae emerge after 7 to 10 days, crawl around for 24–48 h and then drop from the leaves to the ground to search for fine, fibrous roots, switching to larger roots as they mature. These beetles can have as many as 11 instars or as few as 6 which develop over 8 to 15 months. Typically the third to ninth instars are the most active feeders. The total life cycle of D. abbreviatus ranges from less than 1 yr to about 2 yr (Wolcott & French 1936). Larval feeding girdles the root crown area stunting growth and sometimes killing the plant. Adult citrus weevils feeding on young tender leaves produces notches similar to the feeding damage caused by other weevil species or grasshoppers but it is not as damaging as the larval root feeding.
Management tactics for D. abbreviatus in Florida are based mostly on chemical methods (McCoy et al. 2000; Bullock et al. 1988), plant resistance (Lapointe & Bowman 2002), entomopathogenic nematodes (Duncan et al. 2000; McCoy et al. 1995; Schroeder 1990) and use of egg and larval parasitoids (Peña & Amalin 2011; Peña et al. 1998; Sutton et al. 1972). However, no attempts have been made to use predatory insects in an IPM program for citrus root weevil (Peña & Amalin 2011). Control of the larval stages of the citrus root weevil using naturally occurring or commercially available entopathogenic nematodes has been relatively successful in sandy soils. The nematodes are less effective in heavier clay and loam soils than in sandy soil conditions (Duncan & Stelinski 2013; Hall et al. 2001). Studies were conducted at the UF-Citrus Research and Education Center in Lake Alfred, Florida, to determine ‘induced response’ by citrus trees to root feeding damage by citrus root weevil larvae. The use of synthetic attractants in the field to enhance suitable habitat conditions (sandy soils) to attract beneficial nematodes in response to insect attack showed great potential as part of an IPM program (Duncan & Stelenski 2013). Several parasitoids have been introduced and released in Florida by state and federal agencies. Quadrastichus haitiensis Graban (Hymenoptera: Eulophidae), introduced from Puerto Rico, is one of the first egg-parasitoids released (more than 160,000 specimens since 1998) in untreated citrus groves in central and south areas. This parasitoid got successful established and it has been recovered from weevil eggs in Dade, Glades, Hendry, and Polk counties (Weissling et al. 2012). Ceratogramma etiennei Delvare (Hymenoptera: Trichogrammatidae) was released in Florida but its effectiveness in the field has not been determined (Peña & Amalin 2011). Generalist predators, including Euthyrhynchus floridanus (L.), the regal jumping spider, Phidippus regius Koch (Araneae: Salticidae) (Jaffe et al. 1990; Try on 1986), and several predatory ants (Whitcomb et al. 1982) have been reported attacking different stages of the citrus root weevil. Laboratory and greenhouse experiments were conducted by Stuart et al. (2002) with 3 coccinellid species Cycloneda sanguinea (L.), Harmonia axyridis Pallas, and Olla v-nigrum (Mulsant) which are commonly found in the citrus canopy. Results indicated that these coccinellid species have the potential to be used for biological control of citrus root weevil eggs and neonate larvae before they drop to the ground, but their impact needs to be further studied.
Laboratory feeding experiments were conducted exposing adult and nymphal predatory stink bugs Euthyrhynchus floridanus and Podisus maculiventris Say (Heteroptera: Pentatomidae) (Fig. 1) to adult Diaprepes abbreviatus at 25° ± 3 °C, 50–55% RH and 16:8 h L:D. Podisus maculeventris was chosen as a comparative organism because it is a common predatory pentatomid and can be found throughout the citrus growing regions of the USA (De Clercq 2008). Both male and female stink bugs and weevils were utilized. Predators were individually housed with moistened Kimwipe® paper, bean pod, and tissue paper in a Petri dish (14.0 cm × 2.3 cm) for 24 h with no prey. Then, a single (male or female) D. abbreviatus was added to the testing arena as prey. A randomized design with 20 replications was used. Five D. abbreviatus were kept with food and water in Petri dishes with no predators as a control. After 24 h, the number of dead prey was recorded.
Results obtained indicated that E. floridanus males consumed on average (P < 0.05) more D. abbreviatus adults than the E. floridanus females or 3rd-5th instars. All E. floridanus life stages consumed more Diaprepes adults than all life stages of P. maculiventris. There was no significant difference (P > 0.05) in the percentage of Diaprepes male or female adults consumed by the P. maculiventris developmental stages tested (Table 1).
In this study E. floridanus was a more effective predator of D. abbreviatus than P. maculiventris in a laboratory setting (Fig. 2). With further study, E. floridanus may show the potential to augment biological control programs for suppressing populations of citrus root weevil. However, more testing is necessary to determine if this insect actually prefers D. abbreviatus when given a choice.
Laboratory feeding responses of adult and immature Euthyrhynchus floridanus and Podisus Maculiventris to adult Dlaprepes Abbreviatus. in A Randomized Experiment With 20 Replications, A Single Predator in a Petri Dish Was Presented With a Single (male Or Female) D. Abbreviates, and Whether The Latter Was Killed Was Determined After 24 Hours.
The authors thank Bobbie Jo Davis, Julieta Brambila, J. Howard Frank, Paul Skelley and Trevor Smith for reviewing this manuscript. We also thank FDACS-DPI's Biological Control Rearing Facility staff for providing the Diaprepes abreviatus for host feeding tests. This research was approved by the Florida Department of Agriculture and Consumer Services, Division of Plant Industry for publication as contribution #1250.
- R. C. Bullock , C. McCoy , and J. Fojtik 1988. Foliar sprays to control adults of the citrus root weevil complex in Florida. Proc. Florida Hort. Soc. 101: 1–5. Google Scholar
- P. De Clercq 2008. Spined soldier bug, Podisus maculiventris Say (Hemiptera: Pentatomidae: Asopinae), pp. 3,508–3,510 In J. L. Capinera [ed.] Encyclopedia of Entomology, Vol 4. Springer, Heidelberg. Google Scholar
- L. W. Duncan 2000. Burrowing nematodes, pp. 167168 In Otis C. Maloy and Timothy D. Murray [eds.], Encyclopedia of Plant Pathology. John Wiley and Sons, Inc., New York, NY. Google Scholar
- L. Duncan , and L. Stelinski 2013. Targeting Diaprepes root weevil by using native nematodes. Citrus Industry, March, pp. 6–9. Google Scholar
- D. G. Hall , J. Peña , R. Franqui , R. Nguyen , P. Stan sly , C. Mccoy , S. L. Lapointe , C. Adair , and B. Bullock 2001. Status of biological control by egg parasitoids of Diaprepes abbreviates (Coleoptera: Curculionidae) in citrus in Florida and Puerto Rico. BioControl 46: 61–70. Google Scholar
- E. E. Grafton-Cardwell , K. E. Godfrey , J. E. Peña , C. W. Mccoy , and R. F. Luck 2004. Diaprepes root weevil. Univ. California Div. Agric. Nat. Resources. Publ. 8131. 8 pp. Google Scholar
- K. Jaffe , H. Mauleon , and A. Kermarrec 1990. Predatory ants of Diaprepes abbreviatus (Coleoptera: Curculionidae) in citrus groves in Martinique and Guadeloupe, F. W. I. Florida Entomol. 73(4): 684–687. Google Scholar
- K. M. Jetter , and K. Godfrey 2009. Diaprepes root weevil, a new California pest, will raise cost for pest control and trigger quarantines. California Agric. 63(3): 121–126. Google Scholar
- S. L. Lapointe , and K. D. Bowman 2002. Is there meaningful plant resistance to Diaprepes abbreviatus (Coleoptera: Curculionidae) in citrus rootstocks? J. Econ. Entomol. 95: 1059–1065. Google Scholar
- L. Martorell 1976. Annotated food plant catalog of the insects of Puerto Rico. Univ. Puerto Rico Agrie. Exp. Stn., Dept. Entomol. 303 pp. Google Scholar
- C. W. McCoy , D. L. Shapiro, L. W. Duncan , and K. Nguyen 2000. Entomopathogenic nematodes and other natural enemies as mortality factors for larvae of Diaprepes abbreviatus (Coleoptera: Curculionidae). Biol. Control 19: 182–190. Google Scholar
- C. W. McCoy , E. Quintela , S. Simpson , and J. Fojtik 1995. Effect of surface-applied and soil-incorporated insecticides for the control of neonate larvae of Diaprepes abbreviatus in container-grown citrus. Proc. Florida Hort. Soc. 108: 130–136. Google Scholar
- J. E. Peña , and D. M. Amalin 2011. Biological control of Diaprepes abbreviatus by parasitoids. Univ. Florida-IFAS, Tropical Research and Education Center. 9 pp. Google Scholar
- J. E. Peña , J. Etienne , R. Duncan , and J. Pinto 1998. Introduction of Ceratogramma etiennei (Hymenoptera: Trichogrammatidae) for biological control of Diaprepes abbreviatus in Florida, USA, pp. 145–148 In S. A. Hassan [ed.], 5th Intl. Symp. Egg Parasitoids, IOBC. Cali, Colombia. Google Scholar
- W. Schroeder 1990. Suppression of Diaprepes abbreviatus (Coleoptera: Curculionidae) adult emergence with soil application of entomopathogenic nematodes (Nematoda: Rhabditidae). Florida Entomol. 73: 680–683. Google Scholar
- M. Sharia , and J. V. French 2001. Phytophthora disease of citrus associated with root weevils in Texas. Phytopathology 91(6) Suppl. S203. Google Scholar
- S. Simpson , H. Nigg , N. Colie , and R. Adair 1996. Diaprepes abbreviatus Coleoptera: Curculionidae: Hostplant associations. Environ. Entomol. 25(2): 333–349. Google Scholar
- R. J. Stuart , J. P. Michaud , L. Olsen , and W. Mccoy 2002. Lady beetles as potential predators of the root weevil Diaprepes abbrebiatus (Coleoptera: Curculionidae) in Florida Citrus. Florida Entomol. 85: 409–416. Google Scholar
- E. H. Tryon 1986. The striped earwig and ant predators of sugarcane rootstock borer, in Florida citrus. Florida Entomol. 69: 336–343. Google Scholar
- T. J. Weissling , J. E. Peña , R. M. Giblin-Davis , and J. L. Knapp 2012. Diaprepes root weevil. UF-IFAS, Entomol. & Nematol. Dept. Publ. No. EENY-24. 8 pp. Google Scholar
- W. B. Whitcomb , T. D. Go wan , and W. F. Buren 1982. Predators of Diaprepes abbreviatus larvae. Florida Entomol. 65: 150–158. Google Scholar
- M. Wolcott , and J. V. French 1936. The life history of Diaprepes abbreviatus at Rio Piedras, Puerto Rico. J. Agric. Univ. Puerto Rico 20: 883–914. Google Scholar
- R. E. Woodruff 1968. The present status of a West Indian weevil (Diaprepes abbreviatus (L.) in Florida (Coleoptera: Curculionidae). Gainesville: Florida Dept, of Agric. Div. Plant Industry Entomol. Cicular 77. 4 pp. Google Scholar