SciELO - Scientific Electronic Library Online

 
vol.78 número1Cinco especies nuevas de Pselliopus (Hemiptera: Heteroptera: Reduviidae: Harpactorinae: Harpactorini) para MéxicoDiversidad morfológica del sistema de conductos excretores de los peces teleósteos índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • No hay artículos similaresSimilares en SciELO

Compartir


Revista mexicana de biodiversidad

versión On-line ISSN 2007-8706versión impresa ISSN 1870-3453

Rev. Mex. Biodiv. vol.78 no.1 México jun. 2007

 

Taxonomía y Sistemática

 

A pair of new sister species of Loneura from Nicaragua and Venezuela (Psocoptera: Ptiloneuridae)

 

Un par de especies hermanas nuevas del género Loneura, de Nicaragua y de Venezuela (Psocoptera: Ptiloneuridae)

 

Alfonso N. García–Aldrete

 

Departamento de Zoología, Instituto de Biología, Universidad Nacional Autónoma de México. Apartado postal 70–153, 04510 México, D. F.

 

Correspondencia: anga@ibiologia.unam.mx

 

Recibido: 13 septiembre 2006
Aceptado: 12 enero 2007

 

Abstract

Two species of Loneura, one from Nicaragua and the other from Venezuela, are described and illustrated.They constitute a pair of sister species, based on characters of the compound eyes, forewing pterostigma and patternof pigmentation, and structure of male phallosome and hypandrium. Also, they constitute a unique species group in Loneura.

Key words: Psocoptera, Ptiloneuridae, Loneura, sister species, Nicaragua, Venezuela.

 

Resumen

Se describen e ilustran sendas especies de Loneura, de Nicaragua y de Venezuela. Constituyen un par de especies hermanas, con base en caracteres de los ojos compuestos, pterostigma y patrón de pigmentación del ala anterior, y estructura del falosoma e hipandrio del macho. Asimismo, constituyen un grupo de especies único en el género.

Palabras clave: Psocoptera, Ptiloneuridae, Loneura, especies hermanas, Nicaragua, Venezuela.

 

Introduction

To the present, 4 species of Loneura Navás have been recorded in Nicaragua (L. crenata Navás, L. maesi García Aldrete, L. mombachensis García Aldrete, and L. splendida Mockford), and 1 species has been recorded in Venezuela (L. lienhardi García Aldrete) (García Aldrete 2003, 2004, and unpublished personal records). My purpose is to describe and illustrate 2 additional species in the genus, 1 from Nicaragua and another from Venezuela. Theyare closely related, constituting a pair of sister species, unique in that the compound eyes are large and extremely protuberant, the central element of the male hypandriumhas a single posterior projection, bears 2 posterior tufts of long setae and has 2 long, acuminate sclerites associated with it posteriorly, in addition to the pair of lateral sclerites characteristic of most ptiloneurid genera (withthe exception of Ptiloneuropsis Roesler, and Willreevesia García Aldrete –male unknown in Loneuroides GarcíaAldrete–) (Casasola González 2006); in addition, the phallosomes of both species share a similar plan, differing only in small details.

 

Material and methods

The specimens available for study (2 females and 2 males) were dissected in 80% alcohol, and their parts(head, right antenna, right wings, right legs, and genitalia),were mounted on slides in Canada Balsam. Color was recorded by observation of the whole specimen in 80% alcohol under the dissection microscope, illuminated with cold light at 60 X. Measurements, in µm, of parts mountedon slides, were taken with a filar micrometer, whose measuring unit is 136 µm for wings, and 53 µm for other parts. Abbreviations of parts measured (or counted) areas follows: FW: length of right forewing, HW: length ofright hindwing, F: length of right hind femur, T: length ofright hind tibia; t1, t2, t3: length of right hind tarsomeres,ctt1: number of ctenidobothria on t1, Mx4: length offourth segment of right maxillary palpus, f1…fn: length of flagellomeres f1…fn of right antenna, IO: minimumdistance between compound eyes, D: antero–posterior diameter of right compound eye, d: transverse diameter ofright compound eye, PO: d/D. The location of the types isindicated in each description.

 

Descriptions

Loneura jinotegaensis n. sp. (Figs. 1–9)

Female. Color (in 80% alcohol). Body creamy white, withochre spots as indicated below. Compound eyes black,ocelli hyaline, with ochre centripetal crescents; with adark brown band on each gena, from compound eye to each side of epistomal sulcus; postclypeus with oblique dark brown bands. Head pattern (Fig. 1). Scape and pedicel brown, flagellomeres light brown, with distal ends white. Mx4 pale brown, other palpomeres white. Thoracic pleura with irregular ochre spots. Legs pale brown, coxae with proximal and distal dark brown spots, trochanter with brown distal spot; femur with a distal brown spot. Abdomen with transverse, ochre subcuticular rings, less pigmented ventrally. Forewings hyaline, veins brown,pterostigma brown, with a large, central unpigmented area;a slender brown band along wing margin, from R4+5 to distal half of A1, with unpigmented fenestrae along wingmargin (Fig. 2). Hind wings hyaline, veins brown, with brown maculae at the wing margin distally.

Morphology. Outer cusp of lacinial apex broad, with 7–8 denticles. Forewing pterostigma elongate, wider in the middle, slightly projected towards Rs; areola postica tall,apically rounded; Rs 2 branched, M 6 branched (Fig. 2). Hindwing M 4 branched (Fig. 2). Subgenital plate (Fig.8), broad, setose, with pigmented area deeply concave; posterior border straight, with a row of 11 setae directedposteriorly. Gonapophyses (Fig. 4): v1 long, slender, joined to clunium and then bent posteriorly at a right angle; v2+3 with acuminate anterior heel, three setae on distalarea of lobe, and distal projection stout, setose, narrowing distally. Ninth sternum broadly triangular, with side and apical folded areas and a distinct, anterior, transverse pigmented area (Fig. 4). Epiproct broadly triangular, setae apically rounded (Fig. 7). Paraprocts also broadly triangular, setae as illustrated, sensory fields circular, with 28–30 trichobothria issuing from basal rosettes (Fig. 6).

Measurements. FW: 5838, HW: 3945, F: 1188, T: 1432, t1: 687, t2: 129, t3: 173, ctt1: 21, Mx4: 330, f1: 1002, f2:1057, f3: 877, IO: 562, D: 465, d: 399, IO/D: 1.2, PO:0.85.

Male. Color (in 80% alcohol). Same as the female.

Morphology. Outer cusp of lacinial apex as described for the female. Forewing Rs 2 branched, M in right forewing 6 branched, in left forewing eight branched. Min right hindwing 4 branched, in left hindwing 3 branched.Hypandrium (Fig. 9) central sclerite broad, projected posteriorly to form a sclerotized prong, with dense field of long setae on each side adjacent to the posterior margin; other setae as illustrated; side sclerites long, narrow anteriorly, wide and straight posteriorly; a wide based, distally acuminate sclerite, slightly curved outward, on each side of mid prong of central sclerite, posteriorly. Phallosome (Fig.3) with side struts broad, V–shaped; external parameres long, slender, curved, rounded posteriorly; with 2 pairs of symmetric endophallic sclerites, outer pair long, slender, curved, distally parallel to external parameres, each arm with a subapical denticle on inner edge; arising basally from each side of a transverse, smooth, broad pigmented area; inner sclerites with basal thirds slender, curved,strongly sclerotized; distal third dilated, robust, bearing a row of short, blunt protuberances along inner edge. Epiproct (Fig. 5) trapeziform, peripherally with a field of microsetae, wider anteriorly, posterior border with row of 3 short setae, flanked by 2 larger ones; adjacent to anterior margin, medially, a group of 3 setae arranged in a triangle;other setae as illustrated. Paraprocts (Fig. 5), broad, setose,with a field of microspines mesally on outer edge; sensory fields circular, with 29–30 trichobothria issuing from basal rosettes.

Measurements. FW: 5317, HW: 3580, F: 1196, T: 1425,t1: 631, t2: 111, t3: 171, ctt1: 19, f1: 1098, f2: 718, IO:506, D: 543, d: 417, IO/D: 0.93, PO: 0.76.

 

Taxonomic summary

Holotype male, two paratype females. Nicaragua. Jinotega.Peñas Blancas, 1300m. 13°17’N: 85°38’W. 25.VIII.1997.Jean Michel Maes. National Insect Collection (CNIN), Departamento de Zoología, Instituto de Biología, Universidad Nacional Autónoma de México, México City.

Etymology. The specific name makes reference to the type locality.

 

Loneura mirandaensis n. sp. (male). (Figs. 10–15).

Color ( in 80% alcohol). Body creamy white, with ochre spots as indicated below. Compound eyes black, ocelli hyaline, with ochre centripetal crescents. Postclypeus with oblique, brown bands. Mx4 pale brown, other palpomeres white. Scape and pedicel brown, flagellomeres pale brown, with distal ends white. Thoracic pleura with irregular ochre spots. Legs pale brown, coxae with proximal and distal brown spots. Abdomen with dark brown, transverse subcuticular rings, more pigmented dorsally. Forewings hyaline, veins brown. Pterostigma dark brown, with large, unpigmented area on distal half. Slender brown band along wing margin, from R4+5 to distal half of A1, with clear fenestrae next to wing margin as illustrated (Fig. 11). Hindwings hyaline, veins brown.

Morphology. Outer cusp of lacinial apex broad, with 7– 8 denticles. Forewing pterostigma elongate, wider in the middle; areola postica tall, apically rounded; Rs 2 branched, M 6 branched. Hindwing M 5 branched (Fig. 11). Hypandrium (Fig. 15), with central sclerite broad, almost rectangular, projected posteriorly to form a long, sclerotized prong; dense field of long setae on each side, next to posterior margin, other setae as illustrated. Side sclerites long, robust, narrow anteriorly, wide posteriorly. A very wide based sclerite, with a long, acuminate posterior projection, curved outward, on each side of central sclerite, posteriorly. Phallosome (Fig. 12), with side struts broad, V–shaped; external parameres short, crescent shaped, rounded posteriorly. Two pairs of endophallic sclerites, outer pair narrow based, wider in the middle, curved, narrowing distally, basally arising from each side of transverse, low, strongly pigmented triangular area; inner sclerites robust, curved, with proximal halves smooth, basally bent posteriorly, acuminate; distal halves dilated, broad, with row of short, blunt protuberances along inner edge. Epiproct (Fig. 13) trapeziform, with a field of peripheral microspines, wider anteriorly; posterior border with a row of 7 small setae, flanked by 2 larger setae, other setae as illustrated. Paraprocts (Fig. 14), broad, robust, with a field of microspines mesally on outer edge, other setae as illustrated; sensory fields circular, with 23– 24 trichobothria issuing from basal rosettes.

Measurements. FW: 4576, HW: 3162, F: 952, T: 1292, t1: 632, t2: 99, t3: 139, ctt1: 18, Mx4: 261, f1: 1007, f2: 627, IO: 374, D: 500, d: 438, IO/D: 0.74, PO: 0.87.

 

Taxonomic summary

Holotype male. Venezuela. Miranda. Guatopo NP El Lucero, 28 km N Altagracia, 620m. 1–14.VI.1987. UV light trap. J. Peck. Muséum d’Histoire Naturelle, Genève, Switzerland.

Etymology. The specific name refers to the type locality.

 

Remarks

The 2 species described above share several characters that, as a whole, place them close to each other (e. g., large, protuberant compound eyes, shape of the forewing pterostigma and areola postica, pattern of forewing pigmentation, and structure of the male hypandrium and phallosome). Differences between both species are the following: Hindwing M 5 branched in L. mirandaensis vs. hindwing M 4 branched in L. jinotegaensis. Phallosome sclerites more robust, external parameres shorter and more curved, and transverse area between outer sclerites triangular in the former species vs. phallosome sclerites and external parameres slender, and transverse area between outer sclerites not triangular in the latter species. The hypandrium in both species conforms to the same structural plan, but the mid prong of the central sclerite is much longer in L. mirandaensis, and the shapes of the central sclerite and the posterior sclerites are clearly distinct in both species (compare Figs. 9 and 15, and Figs. 3 and 12 for phallosome differences).

The pair of species described above, besides being sister species, clearly constitute a well defined species group in Loneura It is based on the forewing pattern of pigmentation, shape of the pterostigma and areola postica, and structure of the hypandrium and phallosome; the presence of the acuminate sclerites posterior to the central sclerite of the hypandrium, and the tufts on the posterior border of it, are unique in the genus, and are strongly reminiscent of the tufts in the central sclerite of the hypandrium in Ptiloneura bidorsalis Enderlein, which also presents a similar pattern of forewing pigmentation and pterostigma shape. On structure of the hypandrium, 2 additional species groups in Loneura are recognizable: one in which the central piece bears one projection (species included: L. crenata Navás, L. leonilae García Aldrete, and L. mombachensis García Aldrete), and another in which the central piece bears 2 projections (species included: L. amazonica New, L. boliviana Williner, L. erwini New and Thornton, L. maracaensis García Aldrete, L. raramuri García Aldrete, and L. splendida Mockford).

Pairs of closely related species are relatively common in the Psocoptera (e.g., Lachesilla nuptialisL. aethiopica, cf. Badonnel and García Aldrete 1980, several pairs in Goja Navás, cf. Casasola González and García Aldrete 2002, among others).

 

Acknowledgments

I thank Jean Michel Maes (Museo Entomológico de Granada, Nicaragua), for the donation of the specimens of L. jinotegaensis. I also thank Charles Lienhard (Muséum d’Histoire Naturelle, Genève, Suisse), for the loan of the specimen of L. mirandaensis here studied. J. García Figueroa and F. Villegas (Instituto de Biología, UNAM), helped with slide making and plates preparation. I thank the Instituto de Biología, UNAM for continued support of my research throughout the years.

 

Literature cited

Badonnel, A. et A. N. García Aldrete. 1980. Lachesilla nuptialis n. sp., espéce–soeur de Lachesilla aethiopica (Enderlein) (Psocoptera: Lachesillidae). Folia Entomológica Mexicana 44: 5–18.        [ Links ]

Casasola González, J.A. 2006. Phylogenetic relationships of the genera of Epipsocetae (Psocoptera: Psocomorpha). Zootaxa 1194: 1–32.        [ Links ]

Casasola González, J. A. and A. N. García Aldrete. 2002. A taxonomic revision of the genus Goja (Psocoptera: Epipsocidae). Publicaciones Especiales 18. Instituto de Biología, Universidad Nacional Autónoma de México. 143 p.        [ Links ]

García Aldrete, A. N. 2003. New species of Loneura (Ptiloneuridae: Psocoptera), from Argentina, Nicaragua and México. Anales del Instituto de Biología, Universidad Nacional Autónoma de México, Serie Zoología 74: 11–19.        [ Links ]

García Aldrete, A. N. 2004. New species of Loneura (Psocoptera: Ptiloneuridae), from Venezuela and Nicaragua. Anales del Instituto de Biología, Universidad Nacional Autónoma de México, Serie Zoología 75: 143–148.        [ Links ]

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons