Distribution of Species and Species-Groups of Aleiodes (Hymenoptera: Braconidae) in Mexico

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Distribution of Species and Species-Groups of Aleiodes (Hymenoptera: Braconidae) in Mexico Brachystola magna Folia Entorno!. Mex., 41(2): 215-227 (2002) V.M.A.M. Y BERLANGA- DISTRIBUTION OF SPECIES AND SPECIES-GROUPS OF ALEIODES (HYMENOPTERA: BRACONIDAE) IN MEXICO HUGO DELFÍN-GONZÁLEZ1 AND ROBERT A. WHARTON2 'Facultad de Medicina Veterinaria y Zootecnia, Universidad Autonóma de Yucatán, Apartado Postal4-116, Col. ltzimná, 97100 Mérida, Yucatán, México. 2Department of Entomology, Texas A&M University, College Station. Texas 77843, U .S.A. Delf'm-González, H. and R.A. Wharton. 2002. Distribution of species and species-groups of Aleiodes (Hymenoptera: Braconidae) in Mexico. Folia Entorno/. Mex., 41(2): 215-227. ABSTRACT. A study was made of Aleiodes species recorded in Mexico, and specimens deposited in various collections. Using the criteria of Portier and Shaw (1999), eight species groups were recognized from Mexico, with 21 described and 27 undescribed species recorded. These are first records in Mexico for A. earinos Shaw, A. graphicus (Cresson), A. notozophus Marsh and Shaw andA. politiceps (Gahan). The genus is widely distributed in Mexico, being present in 28 of 31 states. Results are discussed in relation to the richness patterns hypotheses of other authors. KEY WoRDs: Aleiodes, Mexico, distribution, Rogadinae, parasitoids. Simposio Control de Plaga de 9- 10 de marzo del2000. Durango, Delfín-González, H. y R.A. Wharton. 2002. Distribución de las especies y grupos de especies de Aleiodes (Hymenoptera: Braconidae) en Mexico. Folia Entorno/. Mex., 41(2): 215-227. RESUMEN. El estudio se realizó con las especies de Aleiodes registradas en México y material depositado en varias colecciones. Utilizando los criterios de Portier y Shaw (1999) se reconocieron ocho grupos de especies presentes en México. Se registraron 21 especies descritas y 27 no descritas. Las especies A. earinos Shaw, A. graphicus (Cresson), A. notozophus Marsh y Shaw y A. politiceps (Gahan) son primeros registros para México. El género muestra amplia distribución en México, estando presente en 28 de los 31 estados. Se discuten los resultados con respecto a las hipótesis de otros autores sobre patrones de riqueza. PALABRAS CLAVE: Aleiodes, México, distribución, Rogadinae, parasitoides. Aleiodes Wesmael, 1838 is a cosmopolitan dae, Pyralidae, Sphingidae, and Tortricidae genus of parasitic wasps. All the species within (Shenefelt, 1975; Shaw and Huddleston, 1991; this genus are koinobiont endoparasitoids of Le­ Shaw, 1995, 1997; Portier, 1997). pidoptera, principally nocturnal, from the fami­ As with other members of the Subfamily Ro­ lies Arctiidae, Bombycidae, Choreutidae, Dre­ gadinae, the majority of these species insert the panidae, Gelechiidae, Geometridae, Hesperii­ ovipositor in the host twice during oviposition. dae, Incurvariidae, Lasiocampidae, Limacodi­ First, to paralyze the host larva by injecting dae, Lycaenidae, Lymantridae, Lyonetiidae, venom into it, and second to introduce their Noctuidae, Notodontidae, Nymphalidae, Psychi- eggs (Shaw, 1983). In someAleiodes species the Delfin-González and Wharton: Distribution of species and species groups of Aleiodes in Mexico venom injection does not occur, appárently to formation on Afrotropical, eastern Palearctic versidad Autónoma de Tamaulip: reduce the risk of the larva falling to the ground and Neotropical species. World-wide, 221 spe­ versity of California, Berkeley ( (Shaw and Huddleston, 1991). cies are known, of which 91 are distributed in sity of California, Davis (UCD] Of the few rogadine species studied, most the Americas, principally in the Nearctic region California, Riverside (UCR); have five larval stages. Of all the braconid spe­ (Shenefelt, 1975; Marsh, 1979; Portier, 1997; Museum of Natural History, Wa cies attacking Lepidoptera, these are the only Shaw, 1997; Shaw et al., 1997; Marsh and Smithsonian (USNM). ones that mummify the host larvae in which they Shaw, 1998; Shaw et al., 1998a and 1998b; Morphology is referenced usil pupate (Shaw and Huddleston, 1991). Aphi­ Marsh and Shaw, 1999 and 2001). Shaw (1997) posed by van Achterberg ( 199: diinae braconids also mummify their host, but estimates that in the Neotropics there are ap­ and Wharton (1997). Material \ they develop exclusively in aphids. In many of proximately 200 undescribed species. A brief using the studies of Shaw (199' the species of Aleiodes, the female wasp ovi­ nomenclatura! history of the 16 Aleiodes species ( 1997), Marsh and Shaw (199~ posits in an early instar, with the wasp larva reported in México has been published by Del­ (1998a, 1998b), Marsh and Sha feeding slowly and not killing the host untillater fín and Wharton (2000). This study constitutes material determined by Dr. Seo instars. The mummy is usually produced during the most complete listing to date, and provides ted in TAMU. the final larval stage of the host but sometimes previously unpublished locality reports. Of the established Aleiodes in earlier instars. There are species of Aleiodes Portier and Shaw ( 1999) review the results of (Portier and Shaw 1999), eight that attack from the first to the fourth larval previous studies (Shaw et al., 1997; Marsh and in México. The synapomorphs t stages (Wallner and Grinberg, 1984; Cave, Shaw, 1998; Shaw et al., 1998a and 1998b; group are as follows: 1995). The mummified host is fixed to the subs­ Marsh and Shaw, 1999), presenting the synapo­ l. apicalis (Brullé) species grot trate by the parasitoid larva through a hole cut morphies that define 17 Aleiodes species groups meter shorter than ocello-ocul in the host integument. Upon emerging, the a­ as monophyletic. The species in the present cipital and hypostomal carina dults cut an emergence opening with uniform study were segregated into groups using these bristle patches on terga 4-7 borders in the extreme posterior, dorsal portion criteria and described in material and methods antennal carina0.55X the dista of the mummified host (Shaw, 1983; Shaw and section. Only the represented species groups clypeus and the antennae ba Huddleston, 1991). The majority of these spe­ were described. fmely granulated or smooth cies are solitary parasitoids that can be attracted heavily pectinate (Shaw et al. by light during the night (Shaw and Huddleston, MATERIAL AND METHODS 2. gastritor (Thunberg) species 1991), though sorne gregarious species are The present study was carried out with mate­ length of pronotum up to 0.3) known, such as A. stigmator (Prana and O'Neil, rial loaned from the following collections: The length (Portier and Shaw, 19S 1994) andA. laphygmae (Cave, 1995). Natural History Museum, London (BMNH); 3. seriatus (Herrich-Schaffer) Rogadines are likely important in control of Colección Entomológica Regional, Universidad Comb of bristles on posterior 1 Lepidoptera infestations in forest and agricultu­ Autónoma de Yucatán (CER-UADY); Colegio tibia (Marsh and Shaw, 1998) ra! environments as they are abundant and de Postgraduados, Montecillo, México (CP); 4. dispar Curtis species group. known species are relatively stenophagous Instituto de Biología UNAM, Estación de Bio­ row, less or equal to 0.29X lf (Shaw, 1995). However, few of these species logía Tropical Charnela (IBUNAM); Museo de 5. praetor (Reinhard) species gr have been studied for pest control uses (see Historia Natural de la Ciudad de México vein RS strongly bent, almo Wallner et al., 1983; Wallner and Grinberg, (MHNCM); Natural History Museum of Los cos-tal margin; lateral ocellm 1984; Cave, 1992 and 1995; Prana and O'Neil, Angeles County (NHMLA); Texas A&M Uni­ greater than the ocello-oc 1994). versity, Insect Collection (T AMU); Colección flagellomere 15 short (Sha" Palearctic and Nearctic Aleiodes species are de Insectos BenéficosEntomófagos, Universidad Portier and Shaw, 1999). well known, whereas there is relatively little in- Autónoma de Nuevo León (CIBE-UANL); Uni- 6. pulchripes (Wesmael) specif 216 of Aleiodes in Mexico Folia Entomol. Mex., 41 (2) 2002 versidad Autónoma de Tamaulipas (UAT); Uni­ claw strongly pectinate, with more than ten versity of California, Berkeley (UCB); Univer­ spines commonly forming the pectin; first me­ sity of California, Davis (UCD); University of tasomal terga weakly rugulose to rugulose­ •'"'''~'''ur in the Nearctic region California, Riverside (UCR); U.S. National costate; third metasomal tergite rugulose to Marsh, 1979; Portier, 1997; Museum ofNatural History, Washington, D.C. rugulose-costate anterior! y and punctate poste­ et al., 1997; Marsh and Smithsonian (USNM). rior! y; lateral ocelli enormous, from 1.5 to et al., 1998a and 1998b; Morphology is referenced using criteria pro­ 9.0X the length of the ocello-ocular distance; 1999 and 2001). Shaw (1997) posed by van Achterberg (1993) and Sharkey malar space shorter than mandible base (Shaw the Neotropics there are ap­ and Wharton (1997). Material was determined et al., 1997). undescribed species. A brief using the studies of Shaw (1997), Shaw et al. 7. gasterator (Jurine) species group. Clypeus of the 16 Aleiodes species (1997), Marsh and Shaw (1998), Shaw et al. has abrupt margin, planar ventrad; oral open­ been published by Del- (1998a, 1998b), Marsh and Shaw, (1999), and ing oval, diameter equal to or slightly greater (2000). This study constitutes material determined by Dr. Scott Shaw deposi­ than malar space; malar space at least equal to listing to date, and provides ted in TAMU. basal width of mandible, usually longer; hind locality reports. Of the established Aleiodes species groups wing marginal cell narrowest at base, widen­ (1999) review the results of (Portier and Shaw 1999), eight
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