Open Access
How to translate text using browser tools
23 January 2020 Exophthalmus cupreipes Champion (Coleoptera: Curculionidae) in Citrus Crops in Mexico
Néstor Bautista-Martínez, Carlos Patricio Illescas-Riquelme, Everardo López-Bautista, Robert W. Jones, José Abel López-Buenfil
Author Affiliations +
Abstract

Exophthalmus cupreipes Champion (Coleoptera: Curculionidae) adult weevils were detected feeding on young leaves and shoots of Persian limes (Citrus latifolia [Tanaka ex Yu. Tanaka] Tanaka; Rutaceae) in commercial plantations in the states of Veracruz and Tabasco, Mexico. Weevil damage to foliage is apparently not significant enough to cause production losses. However, there are reports of related species included in the Exophthalmus genus complex that are considered primary pests of agriculturally important citruses. This study complements the original description by Champion (1911) for adults of both sexes, and provides images of external and internal structures useful for its identification. Moreover, field observations of damage on citrus are presented, and the potential importance as a pest is discussed.

The genus Exophthalmus Schoenherr (Coleoptera: Curculionidae) is a group native to the Neotropics and is widely distributed from Mexico to the Antilles and several countries of Central and South America (Vaurie 1961; O'Brien & Wibmer 1982; Wibmer & O'Brien 1986; Morrone 1999). This taxon comprises at least 95 described species (Zhang 2016) classified within the subfamily Entiminae (Alonso-Zarazaga & Lyal 1999; Morrone 1999). However, there is some difficulty in distinguishing this genus from related genera grouped within the Exophthalmus genus complex, which includes several species belonging to the Eustylini and Geonemini tribes (Vaurie 1961; Franz 2010, 2012).

Exophthalmus adults, like many species of broad-nosed weevils (Entiminae), feed on leaves and shoots as adults, whereas the larvae live in the soil feeding on the roots of several plants (Wright et al. 2003; Oberprieler et al. 2007). The importance of these phytophagous habits is that a large number of species included in the Exophthalmus genus complex (e.g., Diaprepes Schoenherr, Pachnaeus Schoenherr, Compsus Schoenherr, Lachnopus Schoenherr, Exophthalmus; all Coleoptera: Curculionidae) are considered important agricultural pests. Of these, the species that attack commercial citrus plantations in several Central and South American countries are important pests (Vaurie 1961; Schroeder & Beavers 1977; Woodruff 1985; Thomas 2011; O'Brien & Peña 2012).

During entomofaunal inspections in commercial citrus plantations conducted in several citrus-producing regions of Mexico, the presence of the weevil Exophthalmus cupreipes Champion (Coleoptera: Curculionidae) was detected in orchards of Persian lime, Citrus latifolia (Tanaka ex Yu. Tanaka) Tanaka (Rutaceae). This species of weevil was described and classified in the subfamily Otiorhynchinae (now Entiminae) by Champion (1911). Its presence in Mexico is mentioned textually in “Chiapas, Oaxaca, ?Jalapa, ?Córdoba” (Veracruz). Since that report, there practically has been no further information published on this species.

It is unknown whether E. cupreipes represents a potential phytos-anitary problem for citriculture in Mexico, as are other species of this complex in several Neotropical countries. Therefore, the objectives of this study were (1) to complement the existing description of the identifying characteristics of the species, (2) to provide photographs of internal and external structures to facilitate identification, (3) to provide new data on its distribution, and (4) to discuss the damage it causes and its importance in citrus species of agricultural importance.

Materials and Methods

Samples were collected in Persian lime-growing regions of the states of Veracruz and Tabasco, Mexico, where E. cupreipes adults were present. Adults were collected by placing an umbrella turned upside down under the Persian lime tree canopy and vigorously shaking the branches to dislodge the insects, which were then collected from the umbrella. Specimens were preserved in 70% alcohol and labeled by place, date, coordinates, and altitude. Taxonomic identification was carried out with keys by Champion (1911).

In the laboratory, specimens were sexed and counted. Photographs of the body and body parts relevant to the diagnosis were taken with a photomicroscope (Carl Zeiss Tessovar, Oberkochen, Baden-Württemberg, Germany). For extraction of genitalia of the 2 sexes (sternite VII and spermatheca of females, and aedeagus and spicula of males), the abdomen was macerated with 10% KOH at 80 °C in a thermoblock (AccuBlock Digital Dry Bath, Edison, New Jersey, USA) for 20 to 30 min.

Specimens were stored in the collection of the Agricultural Entomology of the Colegio de Postgraduados Campus Montecillo (Texcoco, Estado de Mexico, Mexico); other specimens were donated to the following collections: Colección Entomológica del Instituto de Fitosanidad (CEAM), Colegio de Postgraduados, Campus Montecillo (Texcoco, Estado de Mexico, Mexico); Colección de Curculionoidea (Insecta: Coleoptera) de la Universidad Autónoma de Querétaro (Santiago de Querétaro, Querétaro, Mexico), y Colección Entomológica del Centro Nacional de Referencia Fitosanitaria del Servicio Nacional de Sanidad, Inocuidad y Calidad Agroalimentaria (Tecámac, Estado de Mexico, Mexico).

Results

Exophthalmus cupreipes adults vary greatly in size; generally, the male is smaller than the female (males about 1 cm, females about 1.4 cm). The body is oval shaped, narrower toward the posterior. The sexes can be differentiated by observing the fifth abdominal sternite. In males, the terminal margin is rounded, while in females it is pointed (Fig. 1).

The body is densely covered by iridescent scales; head and legs are copper-colored, and the rest of the body parts are green with golden tones. The cuticle is black or dark brown. The scales of specimens preserved in alcohol change to bluish tones.

The rostrum is longer than wide; the scrobe is long and descends until before the frontal-inferior margin of the eye. Eyes partially encroaching on head and somewhat elongated (Fig. 2A & B). Vibrissae in the lateral pronotum are absent; pronotum slightly flat dorsally; scutelum well developed; humeri rounded, evident (Fig. 2 C). As described by Champion (1911), the elytra have a pair of posteromedian supplementary stria, between striae 5 and 6. However, this is difficult to observe externally because of the abundant scales, but was easily seen internally (Fig. 2E). Legs of all segments without spines in femora and tibiae without denticles (Fig. 2D).

Fig. 1.

Lateral, dorsal, and ventral view of Exophthalmus cupreipes male (left) and female (right). Bar = 1 cm.

img-z2-14_708.jpg

Fig. 2.

Exophthalmus cupreipes. (A) Rostrum dorsal view, (B) rostrum lateral view, (C) base of the pronotum and elytra, (D) metathoracic leg, (E) internal view of elytron (arrow points to supplementary striae), (F) lateral, ventral, and dorsal view of penis (median lobe), (G) sternite IX (spiculum gastrale), (H) spermatheca, (I) sternite VII. Bar = 1 mm.

img-Ajq0_708.jpg

Genitalia of both sexes are elongated and highly sclerotized. Penis (median lobe) moderately curved, and slightly narrower toward the apex (Fig. 2F). Sternite IX (spiculum gastrale) (Fig. 2G) as long as, or slightly longer than, the penis. Shape of spermatheca and sternite VII in Fig. 2 H & I.

Exophthalmus cupreipes was collected on Persian lime in diverse locations in the states of Veracruz and Tabasco (Table 1). Both states are found on the Gulf of Mexico coast and have a mostly hot-humid and hot-subhumid climate. The total number of captured specimens was 116, 61 males and 55 females.

According to our observations, E. cupreipes adults are found during daylight h on foliage and feed only on young leaves and shoots of Persian lime trees (Fig 3A), and females oviposit multiple eggs between 2 citrus leaves cemented together with a clear exudate (Fig. 3B).

Discussion

Other species of Exophthalmus listed for Mexico are Exophthalmus egrestis Boheman, Exophthalmus albidus Champion, Exophthalmus albolineatus Champion, Exophthalmus carinirostris Boheman, Exophthalmus clathratus Champion, Exophthalmus duplicatus Champion, Exophthalmus fasciatus Champion, Exophthalmus interpositus Champion, Exophthalmus lunaris Champion, Exophthalmus nubilus Rosenschoeld, Exophthalmus opulentus Boheman, Exophthalmus roralis Boheman, Exophthalmus verecundus Chevrolat, and Exophthalmus vermiculatus Champion (all Coleoptera: Curculionidae) (O'Brien and Wibmer 1982; Morrone 1999).

Champion (1911) mentions that E. cupreipes is easily distinguished from similar species such as E. opulentus Champion and Exophthalmus vitticollis Champion (Coleoptera: Curculionidae) by the V-shaped protuberance that limits the naked nasal plate. In our study area, other species of Entiminae associated with Persian lime were detected; however, none exhibited characteristics that could confuse it with E. cupreipes.

The information obtained to date in this study, together with the data provided by Champion (1911) (Chiapas and Oaxaca states), suggests that E. cupreipes is limited in its distribution to southeastern Mexico. The potential risk of this weevil is that the lime-growing regions where it was collected are among the most important in terms citrus of production and cultivated area in Mexico.

The damage to foliage is apparently not severe enough to cause production losses, and to date it has not been demonstrated whether the larvae of this weevil feed on citrus roots. However, it is well-known that several species of the Exophthalmus genus complex are considered major pests of citrus.

Table 1.

Distribution of Exophthalmus cupreipes in Veracruz and Tabasco collected on commercial persian lime (Citrus latifolia) plantations.

img-z3-18_708.gif

A similar oviposition behavior has been observed in other species of the Exophthalmus genus complex, including Exophthalmus spp. (Vaurie 1961; Thomas 2011), Diaprepes abbreviatus L. (Coleoptera: Curculionidae) (Peña et al. 2007; Weissling et al. 2019), and Compsus sp. (Peñaloza & Díaz-Riveros 2004).

Howden (1995), lists 11 oviposition categories of Curculionoidea, of which category 2 is described as “eggs placed on leaf surface, covered with exudate.” However, in a further extension of this behavior, E. cupreipes cements the eggs between 2 leaves, a difference that could be considered a unique oviposition category.

Dixon (1954), cited by Vaurie (1961), mentions that in Jamaica several species of Exophthalmus are among the most important citrus, because both adults and larvae feed on the plant, and the latter are more damaging because they affect the roots. The same author states that in sufficient quantities, larvae can damage the main roots and alter the flow of mineral salts to the higher parts of the host, causing the leaves to develop chlorotic appearance, becoming yellow and wilted. According to Vaurie (1961), the 4 species in Jamaica that attack citrus are Exophthalmus vittatus Linnaeus, Exophthalmus similis Drury, Exophthalmus impressus (Fabricius), and Exophthalmus farr Vaurie (all Coleoptera: Curculionidae). Another example of this genus is Exophthalmus jekelianus White (Coleoptera: Curculionidae), which in Costa Rica is considered the second most important pest of Coffea arabica L. (Rubiaceae) after Hypothenemus hampei Wood & Bright (Coleoptera: Curculionidae) (Henderson & Roitberg 2006).

Among the genera related to Exophthalmus, several are considered to be of agricultural importance. Diaprepes abbreviatus L. is one of the most destructive pests in citrus plantations, as well as in several food and ornamental crops in the United States (California, Texas, and Florida) and countries of the Caribbean (Lapointe 2004; Simpson et al. 2006; Jetter & Godfrey 2009; Peña & Amalin 2011). In Colombia, Compsus obliquatus Hustache and Compsus viridivittatus Guérin-Méneville (both Coleoptera: Curculionidae) also are considered citrus pests (O'Brien & Peña 2012).

Another group that includes several species of broad-nosed weevils belonging to the Naupactini tribe affect foliage and roots of Citrus spp. (Rutaceae) plantations cultivated in Brazil (Lanteri et al. 2002; Guedes et al. 2005). Within the tribe Cyphicerini, Myllocerus undecimpustulatus undatus Marshall (Coleoptera: Curculionidae) is an invasive, polyphagous pest native to southern Sri Lanka (George et al. 2015). This species was introduced accidentally into Florida, USA, where it has many reported host plants, including ornamentals, fruit trees, and Valencia oranges (Thomas 2005, Arévalo & Stansly 2009).

It is likely that control methods (mainly pyrethroids, neonicotinoids, and essential oils) used to manage populations of the Asian citrus psyllid, Diaphorina citri Kuwayama (Hemiptera: Liviidae), and the mites Brevipalpus spp. (Acari: Tenuipalpidae) in the study region also reduce populations of E. cupreipes adults, although this needs further study.

Fig. 3.

Exophthalmus cupreipes herbivory (A) and mass eggs (B) on Persian lime leaves.

img-Aflq_708.jpg

We propose giving E. cupreipes the common name “citrus green weevil” (“picudo verde de los cítricos” in Spanish) to facilitate reference for use by growers and technical personnel.

Acknowledgments

Al Servicio Nacional de Sanidad, Inocuidad y Calidad Agroalimentaria (SENASICA) por su apoyo para financiar la presente investigación. A los Comités Estatales de Sanidad Vegetal de los estados de Veracruz y Tabasco por su colaboración en la localización de las plantaciones de limón persa y muestreos en campo.

References Cited

1.

Alonso-Zarazaga MA, Lyal CHC. 1999. A World Catalogue of Families and Genera of Curculionoidea (Insecta: Coleoptera) (Excepting Scolytidae and Platypodidae). Entomopraxis, Barcelona, Spain. Google Scholar

2.

Arévalo HA, Stansly PA. 2009. Suppression of Myllocerus undatus (Coleoptera: Curculionidae) in Valencia orange with chlorpyrifos sprays directed at ground and foliage. Florida Entomologist 92: 150–152. Google Scholar

3.

Champion GC. 1911. Otiorhynchinae Alatae. Biologia centrali-americana, London 4: 178–317. Google Scholar

4.

Dixon WB. 1954. Fiddler beetles. Natural History Notes of the Natural History Society of Jamaica 69: 157–183. Google Scholar

5.

Franz NM. 2010. Redescriptions of critical type species in the Eustylini Lacordaire (Coleoptera: Curculionidae: Entiminae). Journal of Natural History 44: 41–80. Google Scholar

6.

Franz NM. 2012. Phylogenetic reassessment of the Exophthalmus genus complex (Curculionidae: Entiminae: Eustylini, Geonemini). Zoological Journal of the Linnean Society 164: 510–557. Google Scholar

7.

George J, Morse WC, Lapointe SL. 2015. Morphology and sexual dimorphism of the weevil Myllocerus undecimpustulatus undatus (Coleoptera: Curculionidae). Annals of the Entomological Society of America 108: 1–8. Google Scholar

8.

Guedes JVC, Lanteri AA, Parra JRP. 2005. Chave de identificação, ocorrência e distribuição dos curculionídeos-das raízes dos citros em São Paulo e Minas Gerais. Neotropical Entomologist 34: 577–584. Google Scholar

9.

Henderson AE, Roitberg BD. 2006. Microhabitat location of Exophthalmus jekelianus (White) (Coleoptera: Curculionidae): is there a preference for shade-grown coffee? Environmental Entomologist 35: 1603–1609. Google Scholar

10.

Howden AT. 1995. Structures related to oviposition in Curculionoidea. Memoirs of the Entomological Society of Washington 14: 53–100. Google Scholar

11.

Jetter KM, Godfrey K. 2009. Diaprepes root weevil, a new California pest, will raise costs for pest control and trigger quarantines. California Agriculture 63: 121–126. Google Scholar

12.

Lanteri AA, Guedes JC, Parra RP. 2002. Weevils injurious for roots of citrus in São Paulo State, Brazil. Neotropical Entomologist 31: 561–569. Google Scholar

13.

Lapointe SL. 2004. Antecedentes y estrategias para el combate de Diaprepes abbreviatus, plaga invasora del Caribe. Manejo Integrado de Plagas y Agroecología 71: 106–111. Google Scholar

14.

Morrone JJ. 1999. The species of Entiminae (Coleoptera: Curculionidae) ranged in America south of the United States. Anales del Instituto de Biología, Universidad Nacional Autónoma de México, Serie Zoología 70: 99–168. Google Scholar

15.

O'Brien CW, Wibmer GJ. 1982. Annotated checklist of the weevils (Curculionidae sensu lato) of North America Central America, and the West Indies (Coleoptera: Curculionoidea). Memoirs of the American Entomological Institute 34: 1–382. Google Scholar

16.

O'Brien CW, Peña JE. 2012. Two species of Compsus Schoenherr, new citrus pests from Colombia (Coleoptera: Curculionidae: Entiminae). Insecta Mundi 0227: 1–13. Google Scholar

17.

Oberprieler RG, Marvaldi AE, Anderson RS. 2007. Weevils, weevils, weevils everywhere. Zootaxa 1668: 491–520. Google Scholar

18.

Peña JE, Amalin DM. 2011. Biological control of Diaprepes abbreviatus by parasitoids. University of Florida/IFAS, Tropical Research and Education Center, Fort Pierce, Florida, USA. Google Scholar

19.

Peña JE, Amalin DM, Husenberg A, Mannion C. 2007. Egg distribution and sampling of Diaprepes abbreviatus (Coleoptera: Curculionidae) on silver buttonwood. Florida Entomologist 90: 234–237. Google Scholar

20.

Peñaloza MC, Díaz-Riveros G. 2004. Así se Maneja y Controla el Picudo de los Cítricos Compsus sp. Ministerio de Agricultura y Desarrollo Rural, Instituto Colombiano Agropecuario, Bogotá, Colombia. Google Scholar

21.

Schroeder WJ, Beavers JB. 1977. Citrus root weevils in Florida: identification, biology and control. Proceedings of the International Society of Citriculture 2: 498–500. Google Scholar

22.

Simpson SE, Higg HN, Coile NC, Adair RA. 1996. Diaprepes abbreviatus (Coleoptera: Curculionidae): host plant associations. Environmental Entomologist 25: 333–349. Google Scholar

23.

Thomas MC. 2005. Myllocerus undatus Marshall, a weevil new to the Western Hemisphere. Pest Alert #DACS-P-01653. Florida Department of Agriculture & Consumer Services, Division of Plant Industry, Gainesville, Florida, USA. Google Scholar

24.

Thomas MC. 2011. Exophthalmus similis Drury (Coleoptera: Curculionidae), a Jamaican citrus pest newly discovered in the Bahamas. Pest Alert #DACSP-01766 (illustrations, records). Florida Department of Agriculture & Consumer Services, Division of Plant Industry, Gainesville, Florida, USA. Google Scholar

25.

Vaurie P. 1961. A review of the Jamaican species of the genus Exophthalmus (Coleoptera, Curculionidae, Otiorhynchinae). American Museum Novitates 2062: 1–41. Google Scholar

26.

Weissling TJ, Peña JE, Giblin-Davis RM, Knapp JL. 2019. Diaprepes root weevil, Diaprepes abbreviatus (Linnaeus) (Insecta: Coleoptera: Curculionidae). Featured Creatures #EENY-024. University of Florida/IFAS, Entomology and Nematology Department, Gainesville, Florida, USA. Google Scholar

27.

Wibmer GJ, O'Brien CW. 1986. Annotated checklist of the weevils (Curculionidae sensu lato) of South America (Coleoptera: Curculionoidea). Memoirs of the American Entomological Institute 39: 1–563. Google Scholar

28.

Woodruff RE. 1985. Citrus weevils in Florida and the West Indies: preliminary report on systematics, biology, and distribution (Coleoptera: Curculionidae). Florida Entomologist 68: 370–379. Google Scholar

29.

Wright GA, Simpson SJ, Raubenheimer D, Stevenson PC. 2003. The feeding behavior of the weevil, Exophthalmus jekelianus, with respect to the nutrients and allelochemicals in host plant leaves. Oikos 100: 172–184. Google Scholar

30.

Zhang G, Basharat U, Matzke N, Franz NM. 2016. Model selection in statistical historical biogeography of Neotropical insects–the Exophthalmus genus complex (Curculionidae: Entiminae). Molecular Phylogenetics and Evolution 109: 226–239. Google Scholar
Néstor Bautista-Martínez, Carlos Patricio Illescas-Riquelme, Everardo López-Bautista, Robert W. Jones, and José Abel López-Buenfil "Exophthalmus cupreipes Champion (Coleoptera: Curculionidae) in Citrus Crops in Mexico," Florida Entomologist 102(4), 708-712, (23 January 2020). https://doi.org/10.1653/024.102.0406
Published: 23 January 2020
KEYWORDS
broad nosed weevil
citrus green weevil
Exophthalmus genus complex
Back to Top