versión On-line ISSN 2007-8706
versión impresa ISSN 1870-3453
Rev. Mex. Biodiv. vol.81 no.3 México dic. 2010
Taxonomía y sistemática
The Central American genus Aporolaus, new status and taxonomic revision (Coleoptera: Scarabaeoidea: Hybosoridae: Hybosorinae)
El género centroamericano Aporolaus, nuevo estatus y revisión taxonómica (Coleoptera: Scarabaeoidea: Hybosoridae: Hybosorinae)
Federico C. Ocampo
Laboratorio de Entomología, Instituto de Investigaciones de las Zonas Áridas, CCTCONICET, C.C. 507, 5500 Mendoza, Argentina. Correspondent: firstname.lastname@example.org
Recibido: 25 septiembre 2009
Aceptado: 03 noviembre 2009
The hybosorine genus Aporolaus Bates is taxonomically revised. The genus was previously considered as synonym of Dicraeodon Erichson and, based on a detailed morphological study, is reinstated herein. A generic description and diagnosis for A. fimbriatus Bates, the only known species in the genus, is provided along with illustrations of diagnostic characters. A lectotype is designated for A. fimbriatus Bates.
Key words: Central America, Hybosoridae, taxonomy, Aporolaus.
Se provee una revisión taxonómica del género de Hybosorinae Aporolaus Bates. Este género era considerado sinónimo de Dicreaeodon Erichson, pero en base a un estudio detallado de su morfología es reestablecido en esta contribución. Se proporciona una descripción y diagnosis de A. fimbriatus, la única especie conocida del género, así como ilustraciones de caracteres diagnósticos. Se designa un lectotipo para A. fimbriatus Bates.
Palabras clave: América Central, Hybosoridae, taxonomía, Aporolaus.
The Central American hybosorine genus Aporolaus was described by Bates (1887) for 1 species, A. fimbriatus Bates (1887). Later, Arrow (1911) synonymized Aporolaus with Dicraeodon Erichson (1847), based on the resemblance of the females of A. fimbriatus and D. basalis (Westwood). Aside of being listed in catalogs (Arrow, 1912; Ratcliffe, 2002; Ocampo and Ballerio, 2006), A. fimbriatus has not been treated taxonomically since its original description. After a detailed analysis of the morphology of Dicraeodon species, including new undescribed taxa, I propose to reinstate the genus Aporolaus.
The objective is to provide a taxonomic revision of the genus Aporolaus and the species, A. fimbriatus, as well provide illustrations of diagnostic characters and a distribution map.
Materials and methods
Body measurements, puncture density and size, and density of setae are based on the following standards. Body length was measured from the apex of the pronotum (at the middle) to the apex of the elytra. Body width was measured across the elytra at the middle. Puncture density was considered "dense" if punctures were nearly confluent to less than 2 puncture diameters apart, "moderately dense" if punctures were 2 to 6 diameters apart, and "sparse" if punctures were more than 6 diameters apart. Puncture size was defined as "small" if punctures were 0.02 mm or smaller, "moderate" if 0.020.07 mm, and "large" if 0.07 mm or larger. Setae were defined as "sparse" if there were few setae, "moderately dense" if the surface was visible but with many setae, and "dense" if the surface was not visible through the setae. Elytral carinae were counted from the elytral suture, with the elytral suture included. Description of hind wing venation was done following Ocampo (2003, 2006). Specimen label data was copied verbatim using "/" between the lines of the labels.
This study was based on specimens from the following institutions (with curators given in brackets):
IAZA Instituto Argentino de Investigaciones de Zonas Áridas, Mendoza, Argentina (F. C. Ocampo).
INBC Instituto Nacional de Biodiversidad (InBio), Santo Domingo de Heredia, Costa Rica (A. Solís).
BMNH The Natural History Museum, London, England (M. Kerley).
CASC California Academy of Sciences, San Francisco, USA (R. Brett).
UNSM University of Nebraska State Museum, Lincoln, Nebraska, USA (B. Ratcliffe).
USNM United States National Collection, Washington DC, USA (David Furth), currently at the University of Nebraska, Lincoln (B. Ratcliffe, M. L Jameson).
UVGC Universidad del Valle de Guatemala, Guatemala City, Guatemala (J. Schuster).
ZMHB Museum für Naturkunde der Humboldt Universität, Berlin, Germany (H. Wendt).
Type species Aporolaus fimbriatus Bates 1887: 129 (pl. 2), by monotypy.
Diagnosis. It can be distinguished from Dicraeodon and all other Hybosorid genera in the New World by the following combination of characters: labral anterior margin with tooth at middle; with strongly protruding mandibles in males, each mandible bearing a dorsal tooth and 2 apical teeth; antennal club with basal antennomere cupshaped; posterior angles of pronotum broadly rounded; hind wing with MP3 vein present and lacking MP4 vein; meso and metatibiae lacking transversal carinae; tarsal claws simple (lacking ventral tooth or indentation); and male genitalia are strongly asymmetrical.
Systematic position. Phylogenetic relationships of Aporolaus have been never discussed. A preliminary cladistic analysis based on morphological data indicates that it may constitute a basal lineage in the subfamily Hybosorinae (Ocampo, unpublished).
Aporolaus fimbriatus Bates, 1887: 130 (pl. 2).
Dicraeodon fimbriatus; Arrow, 1911 (synonymy), 1912: 39 (cat.); Ratcliffe, 2002: 32 (cat.); Ocampo and Ballerio, 2006: 191 (cat.).
Type material. Lectotype at MNHN labeled: "Bugaba / Panama / Champion."; "B.C.A. Coleccion, II (2) / Aporolaus / fimbriatus / cotypus"; "Museum Paris / 1936 / Coll. A. Boucomont"; "Aporolaus/ fimbriatus / Bates / LECTOTYPE / F. C. Ocampo det." Lectotype here designated. One paralectotype at MNHN labeled as Lectotype. Two paralectotypes at CNCI labeled as lectotype except: "COTYPE / CNCN° 8754 / A. fimbriatus / Bates." Two paralectotypes at CNCI labeled: "Bugaba / 8001,500 ft. / Champion"; "B.C. A. / duplicates"; "COTYPE / CNCN° 8754 / A. fimbriatus / Bates." One paralectotype at CNCI labeled: "Bugaba / 8001,500 ft. / Champion"; "male symbol"; "B.C.A. Coleccion, II (2) / Aporolaus / fimbriatus / cotypus". Four paralectotypes at ZMHB labeled: "Bugaba / 8001,500 ft. / Champion". Two paralectotypes at CASC labeled: "Bugaba / 8001,500 ft. / Champion"; "male symbol"; "Collection / Biologia Cent / Americana"; "PARATYPE / Aporolaus / fimbriatus/ H. W. Bates". Three parelectotypes at AMNH labeled: "Bugaba / 8001,500 ft. / Champion"; "Donated by F. du C. Godman / 1907". All paralectotypes labeled: "Aporolaus / fimbriatus / Bates / PARALECTOTYPE / F. C. Ocampo det.".
Type Locality. PANAMA: Chiriqui, Bugaba.
Distribution (Fig. 7). COSTA RICA: Sabalito, CotoBrus (1). PANAMA. Chiriqui: Bugaba (15); Santa Clara (2 km N) (3); Santa Clara (4); Río Sereno (15 km E) (1); Río Sereno "Area" (4); vic Hornito (2); Continental divide trail (2). Distribution localities are placed between 10001500 m in altitude.
Male (Figs. 1, 3) and female (Figs. 2, 4). Length 5.507.15 mm; width 3.043.75 mm. Color: Head black, pronotum light brown to dark brown, elytra light brown, some specimens bicolored light brown at elytral basal half and dark brownblack on apical half. Head (Figs. 34): Frons convex; surface smooth in middle, punctate on sides; punctures moderately dense, size moderate. Frontoclypeal suture obsolete. Clypeal shape subtrapezoidal, anterior margin broadly rounded, surface punctate, punctures moderately dense. Clypeal anterior margin weakly reflexed, setose, setae moderately dense. Labrum broadly rounded, with middle tooth at apex; dorsal surface with fringe of setae on anterior margin. Mandibles protruding beyond labral apex, dorsoventrally flat; with 1 dorsal tooth at middle and 2 teeth at apex, dorsal tooth slightly reflexed (males), or with 2 apical teeth (females). Labium with apex of mentum slightly indented, surface sparsely setose, setae long, labial palps with 3 palpomeres. Maxilae with lacinia densely setose at apex (males) or lacking setae at apex (females), maxillary palps with 4 palpomeres. Eyes small, visible in dorsal view. Antennae with 9 antennomeres; antennomeres 27 moniliform; antennal club with 3 antennomeres; basal antennomere of club cupshaped, capable of receiving penultimate and ultimate antennomeres (Fig. 4). Pronotum (Figs. 1, 2): Surface mostly convex, base flat in middle, pronotum 0.6 times as long as wide; surface mostly sparsely to moderately punctate; punctures moderate in size. Anterior margin with weak bead and membrane well developed; lateral margins broadly rounded, beaded, finely denticulate with long setae; posterior margin slightly sinuous in middle. Anterior angles acute; posterior angles broadly rounded. Scutellum: Shape triangular, surface moderately setose. Elytron (Figs. 1, 2): Globose, apex rounded; surface with 12 fine, punctate striae, lateral striae only visible on apical third; interval surface smooth. Lateral margin setose, setae long slender at base, becoming shorter toward apex. Epipleuron smooth, wider at base, tapered toward apex. Hind wing: With MP3 vein developed, MP4 not developed, MCu loop well developed. Venter: pro, meso, and metasternum and abdominal sternites surface smooth, sparsely setose, setae long, slender; prosternal shield with posteriomedial process not developed. Legs (Figs. 1, 2): Protibia with 3 teeth and small denticles on outer margin; basal tooth small, middle and apical teeth well developed, curved; tibial dorsal surface with 2 setose, longitudinal carinae, outer margin setose setae moderately long; protibial spur shorter than apical tibial tooth, strongly curved, apex acute. Meso and metatibia lacking transversal carina (few specimens with poorly developed carinae on metatibia); with 2 apical, acuminate spurs. Metatibia outer margin straight (males) or slightly curved (females). Pro, meso, and metatarsomeres 1 longer than 2; tarsomeres 24 subequal in length; tarsomere 5 longer than 4. Pro, meso, and metatarsal claws as long as tarsomeres 5, simple, curved. Meso and metatibial outer surface with 3 longitudinal rows of setae; setae slender to thick. Male genitalia asymmetrical (Figs. 5, 6).
I am grateful to the curators and collection managers listed in the material and methods section for loans of specimens and facilitating the material for this study. This project was supported by NSF (The National Science Foundation, USA) through the following grants: Advances in Biological Informatics # 0743783, and AToL # EF0531768, and by CONICET (Consejo Nacional de Investigaciones Científicas y Técnicas, Argentina) through the grant PIP #11220080101869. Finally, I thank CONICET and the Instituto de Ciencias Básicas (ICB), Universidad Nacional de Cuyo, for their permanent support to my research.
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