Open Access
How to translate text using browser tools
1 December 2008 Geographic range expansion of Oxyops vitiosa (Coleoptera: Curculionidae) to the Bahamian Archipelago
Paul D. Pratt, Min B. Rayamajhi, Ted D. Center
Author Affiliations +

The Australian tree Melaleuca quinquenervia (Cav.) Blake was internationally disseminated over the last century for ornamental and agroforestry purposes (Dray et al. 2006). Although introduced into California, Texas, and Louisiana, it has not been reported as an invasive pest in those areas. In contrast, it has proven to be a superior competitor to most native vegetation in wetlands of Florida, Puerto Rico, Cuba, and the Bahamas (Pratt et al. 2005b; Pratt et al. 2007; Turner et al. 1998).

A biological control program in Florida targeting M. quinquenervia was initiated in 1986 (Balciunas et al. 1994). The weevil Oxyops vitiosa Pascoe and the psyllid Boreioglycaspis melaleucae Moore were among the first natural enemies selected for pre-release risk assessments (Purcell & Balciunas 1994). Host range testing indicated that both herbivores only completed development on a small group of species in the Melaleuca genus, of which there are no native representatives in the New World. The weevil and psyllid were permitted for release in south Florida during the spring of 1997 and 2002, respectively. Both species established in M. quinquenervia dominated habitats (Pratt et al. 2003; Center et al. 2007).

Herbivory from introduced biological control agents resulted in significant reductions in M. quinquenervia growth, reproduction, and survivorship (Pratt et al. 2005a; Franks et al. 2006; Morath et al. 2006; Center et al. 2007; Tipping et al. 2008). These impacts collectively limited the competitive superiority of M. quinquenervia and led to increases in native species diversity in habitats once dominated by it. In response, federal, state, and county agencies initiated a redistribution campaign for O. vitiosa and B. melaleucae. To date, >3 million individuals have been redistributed to nearly 407 locations in southern Florida.

Biotic exchange between the Florida mainland and neighboring island systems is an increasingly common occurrence (Dobbs & Brodel 2004). We questioned whether O. vitiosa and/or B. melaleucae had dispersed to the neighboring West Indies. To address this question we surveyed M. quinquenervia dominated wetlands of Puerto Rico and discovered the presence of B. melaleucae in 2006 (Pratt et al. 2007). The occurrence of the psyllid in Puerto Rico, some 1300 km from the originating population in Florida, led us to hypothesize that the Australian herbivores may have dispersed to M. quinquenervia stands on the nearby islands of the Bahamian archipelago.

Recent aerial and ground vegetation assessments quantified the geographic distribution of several exotic plant species, including M. quinquenervia, on Grand Bahama, New Providence, and Andros islands of the Bahamas (Fig. 1; Pratt et al. 2007). Using coordinates from these assessments, we surveyed all known M. quinquenervia populations or individuals for the Australian herbivores during Dec 2005 and Mar 2007. Trees were examined by 3 observers for 15 min each to detect presence, estimate feeding damage, and determine the proportion of trees infested. Feeding damage was assessed on a 5-point scale based on visual estimation of percentage of suitable foliage destroyed by feeding: 0 = no damage; 1 = <25% destroyed; 2 = 26 to 50%; 3 = 51 to 75%; 4 = 76 to 100% destroyed. The proportion of damaged trees within a given site was estimated and averaged within site.

Eight sites on Andros, 22 on Grand Bahama, and 20 on New Providence containing M. quinquenervia were surveyed (Fig. 1). No evidence of either insect was observed in the 2005. Similarly, B. melaleucae was absent in the 2007 survey but O. vitiosa was observed at 6 locations on New Providence (Fig. 1). Identification of O. vitiosa was confirmed by Mike Thomas (Florida Department of Agriculture and Consumer Services, Gainesville, FL) and voucher specimens were deposited in the Florida State Collection of Arthropods.

Geographic distribution of O. vitiosa was limited to the southern half of New Providence (Fig. 1). Herbivory was greatest at site 1, with M. quinquenervia trees experiencing 25-50% damage, and having the highest proportion of trees attacked by the weevil (60%). Less than 10% of trees were damaged at the 5 other sites. If we assume that damage levels and the proportion of trees attacked correlate with time since establishment, these data suggest a point of introduction for O. vitiosa at or near the village of Adelaide and adults spread from these trees to surrounding M. quinquenervia stands.

Discovery of O. vitiosa in the Bahamas raises questions regarding pathways of introduction. How might O. vitiosa disperse from Florida to New Providence? Proximity and widespread occurrence of M. quinquenervia among the Bahamian islands may have allowed unassisted dispersal from Florida. It is possible that hurricanes facilitate dispersal of insects through the Caribbean (Drake & Farrow 1988). Hurricane Wilma in Oct 2005 crossed southern Florida and made landfall in the Bahamas. New Providence lies approximately 300 km east of Miami but Grand Bahama and Andros are 130 and 230 km, respectively, from the mainland, suggesting that under natural dispersal scenarios it is more likely that O. vitiosa would reach one of the near islands first.

Frequency of trade and tourism may have aided weevil establishment. Human activities play an important role in accidental insect invasions, particularly with international transportation of airplane luggage and cargo (Kiritani & Yamamura 2003). Nearly 32,000 flights departed Florida for the Bahamas in 2006, and nearly 22,900 of these arrived on the 3 islands studied herein (US Department of Transportation 2008). Within the Bahamas, the number of annual flights to New Providence was markedly greater (16,576) than those destined for Grand Bahama (5,688) or Andros (600). The frequent transport of tourists and cargo between southern Florida and New Providence makes the premise that O. vitiosa was inadvertently carried or “hitchhiked” to the island a plausible explanation. Of greater concern is the possibility that O. vitiosa may have been intentionally smuggled into the Bahamas to facilitate control efforts of M. quinquenervia.

While the invasion pathway of O. vitiosa remains uncertain, occurrence of the weevil in the Bahamas draws attention to potential movement of biological control agents beyond their intended range. Thus, biological control programs must consider risks to the flora of neighboring regions, especially if those regions harbor populations of the target host. Host range testing and post release field studies indicate that development of O. vitiosa is restricted to M. quinquenervia and closely related congeners, and is therefore unlikely to pose a threat to flora of the Bahamas. Host range testing of O. vitiosa addressed the biogeographic overlap of M. quinquenervia with Florida’s neighboring regions by including genera that represented much of the Caribbean myrtaceous diversity. Ten of the 11 native Bahamian myrtaceous species were included in the O. vitiosa host range studies and all were non-hosts (Correll & Correll 1982).


The Australian weevil Oxyops vitiosa is a specialized herbivore of Melaleuca quinquenervia and closely related congeners. The weevil was intentionally introduced into Florida, USA in 1997 and was recently discovered on the Bahamian island of New Providence, some 300 km east, feeding on naturalized M. quinquenervia trees. The weevil has colonized M. quinquenervia stands in the southern part of the island and is expected to spread to all invaded habitats. Oxyops vitiosa is unlikely to harm native plant species but will affect ornamental landscape plantings of M. quinquenervia.

References Cited


J. K. Balciunas, D. W. Burrows, and M. F. Purcell . 1994. Field and laboratory host ranges of the Australian weevil, Oxyops vitiosa, a potential biological control agent of the paperbark tree, Melaleuca quinquenervia. Biol. Control 4:351–360. Google Scholar


T. D. Center, P. D. Pratt, P. W. Tipping, M. B. Rayamajhi, T. K. Van, S. Wineriter, and F. A J. Dray . 2007. Initial impacts and field validation of host range for Boreioglycaspis melaleucae Moore (Hemiptera: Psyllidae), a biological control agent of the invasive tree Melaleuca quinquenervia (Cav) Blake. Environ. Entomol 36:569–576. Google Scholar


D. S. Correll and H. B. Correll . 1982. Flora of the Bahama Archipelago. J. Cramer, Vaduz, Liechtenstein. Google Scholar


T. T. Dobbs and C. F. Brodel . 2004. Cargo aircraft as a pathway for the entry of nonindigenous pests into south Florida. Florida Entomol 87:65–78. Google Scholar


V. A. Drake and R. A. Farrow . 1988. The influence of atmospheric structure and motions on insect migration. Annu. Rev. Entomol 33:183–210. Google Scholar


F. A. Dray, B. C. Bennett, and T. D. Center . 2006. Invasion history of Melaleuca quinquenervia (Cav.) S.T. Blake in Florida. Castanea 71:210. Google Scholar


S. J. Franks, A. M. Kral, and P. D. Pratt . 2006. Herbivory by introduced insects reduces growth and survival of Melaleuca quinquenervia seedlings. Environ. Entomol 35:366–372. Google Scholar


K. Kiritani and K. Yamamura . 2003. Exotic insects and their pathways for invasion. pp. 44-67 In G. M. Ruiz and J. T. Carlton [eds.], Invasive Species: Vectors and Management Strategies. Island Press, Washington. Google Scholar


S. U. Morath, P. D. Pratt, C. S. Silvers, and T. D. Center . 2006. Herbivory by Boreioglycaspis melaleucae (Hemiptera: Psyllidae) accelerates foliar degradation and abscission in the invasive tree Melaleuca quinquenervia. Environ. Entomol 35:1372–1378. Google Scholar


P. D. Pratt, V. Quevedo, L. Bernier, J. Sustache, and T. DCenter . 2005b. Invasions of Puerto Rican wetlands by the Australian tree Melaleuca quinquenervia. Caribbean J. Sci 41:42–54. Google Scholar


P. D. Pratt, M. B. Rayamajhi, C. S. Silvers, and A. Ferriter . 2007. Naturalization and biomass allocation of the invasive tree Melaleuca quinquenervia in wetlands of the Bahamas. J. Aquatic Plant Manage 45:8–16. Google Scholar


P. D. Pratt, M. B. Rayamajhi, T. K. Van, T. D. Center, and P. W. Tipping . 2005a. Herbivory alters resource allocation and compensation in the invasive tree Melaleuca quinquenervia. Ecol. Entomol 30:316–326. Google Scholar


P. D. Pratt, D. H. Slone, M. B. Rayamajhi, T. K. Van, T. D. Center, D. H. Slone, and M. B. Rayamajhi . 2003. Geographic distribution and dispersal rate of Oxyops vitiosa (Coleoptera: Curculionidae), a biological control agent of the invasive treeMelaleuca quinquenervia in south Florida. Environ. Entomol 32:397–406. Google Scholar


M. F. Purcell and J. K. Balciunas . 1994. Life history and distribution of the Australian weevil Oxyops vitiosa, a potential biological control agent for Melaleuca quinquenervia. Ann. Entomol. Soc. America 87:867–873. Google Scholar


P. W. Tipping, M. R. Martin, P. D. Pratt, T. D. Center, and M. B. Rayamajhi . 2008. Suppression of growth and reproduction of an exotic invasive tree by two introduced insects. Biol. Control 44:235–241. Google Scholar


C. E. Turner, T. D. Center, D. W. Burrows, and G. R. Buckingham . 1998. Ecology and management of Melaleuca quinquenervia, an invader of wetlands in Florida, U.S.A. Wet. Ecol. Manag 5:165–178. Google Scholar


US Department of Transportation 2008. Research and Innovative Technology Administration, Bureau of Transportation Statistics. Scholar

Fig. 1.

Geographical distribution of the invasive tree M. quinquenervia (grey points) and the Australian weevil O. vitiosa (numbered stars) in the Bahamas.

Paul D. Pratt, Min B. Rayamajhi, and Ted D. Center "Geographic range expansion of Oxyops vitiosa (Coleoptera: Curculionidae) to the Bahamian Archipelago," Florida Entomologist 91(4), 695-697, (1 December 2008).
Published: 1 December 2008
Back to Top