Oligoneuria macabaiba sp. nov. (Insecta: Ephemeroptera) from Brazil.
A new species of Oligoneuria from Brazil is herein described based on male and female imagos from the Atlantic Rainforest. Despite several attempts, no nymph was found on collecting sites but adult's characteristics are enough to place specimens on this genus. The new species possess the distinctive membranous extension on front of the head and wing venation similar to that of Oligoneuria, but rather different male genitalia. Diagnosis of Oligoneuria is, therefore, altered to comprise this difference. The new species represents the first record of the genus from Southeastern Brazil.
MATERIAL AND METHODS
Imagos from both sexes where caught on light traps in the municipality of Macae, Rio de Janeiro State. Specimens were preserved in 80% ethanol. Males and females were collected on same swarm. Searching was made in the Macae river, but after several attempts nymphs were not found. Interpretation of wing veins was based on Kluge (2004, 2007). Type material is deposited at Colecao Entolomogica Professor Jose Alfredo Pinheiro Dutra (DZRJ) -- Departamento de Zoologia, Universidade Federal do Rio de Janeiro (UFRJ). Drawings were made under a stereoscopic microscope with camera lucida. Collecting sites were marked with a GPS using the datum WGS84.
Oligoneuria macabaiba sp. nov.
Diagnosis: Oligoneuria macabaiba sp. nov. can be recognized by the following combination of characteristics: (1) hind wings with CuA curved apically; (2) faintly marked cross veins basal to CuA of hind wing; (3) posterolateral spines on abdominal segment II not well developed, restricted to a small projection; (4) male styliger plate almost rectangular, without well developed posterolateral projections; (5) male genitalia with two divergent sclerotized spines, directed posterolaterally, and a median membranous area, divided into two lobes (as in figure 3).
Male Imago (Holotype): Length: body 14.0mm; fore wing 10.5mm; hind wing 5.7mm.
Head: Area between eyes and ocelli whitish suffused with gray. Margins of head black. Head ventrally covered by a membranous black extension. Eyes black. Ocelli white surrounded by black ring at base. Base of antennae whitish; scape whitish possessing incomplete wide blackish ring; pedicel and flagellum brownish.
Thorax: Pronotum whitish; meso and metanota yellowish; terga with scattered brownish stains. Membranous filaments of mesonotum short. Prosternum whitish; meso and metasterna yellowish; sterna with scattered brownish stains.
Wings: Membrane of wings translucent whitish; bearing several microtrichia. Fore wings with cross veins ranging from base to apex of C and Sc area and from base to almost apex of [R.sub.1] and [R.sub.3] area (Fig. 1). Hind wings with cross veins basally on C and Sc area and [R.sub.1] and [R.sub.3] area. Vein CuA curved apically; faint cross veins present basal to CuA of hind wing (Fig. 2).
Legs: Forelegs whitish, femora with two brownish longitudinal stripes; tibiae and first two segments of tarsi shaded with brown. Forelegs with three tarsal segments, first two segments same in length, third longer, more than twice the length of first two tarsomeres. Remaining legs with yellowish femora, possessing a brown wide basal band and a narrow apical band; tibiae and last tarsomere of each leg whitish; tibiae with basal mark and inner margin brownish. Mid and hind tarsi with four segments, first and last tarsomeres more than twice as long as second and third tarsomeres together. Tarsal claws blunt.
Abdomen: Posterolateral spines present on segments II-IX; only a small projection on segment II; spines more developed on remaining segments. All spines flexible ("twisted" according to Salles et al. 2007), except those on tergum IX. Terga reddish brown. Terga with median fainted longitudinal line, light colored (Fig. 4). Sterna whitish, shaded with reddish brown.
Genitalia: Styliger plate straight, not projected. Segment I of forceps with inner margin possessing several short setae on apical half. Penes divided into two membranous lobes, each possessing a posterolaterally directed spine on outer margin (Fig. 3). Caudal filaments whitish with brown annulations, subequal in length, with row of long setae on junctions.
Variations: Length: body 13.0mm14.6mm; forewing 10.0mm-10.8mm; hind wing 5.4-5.7mm. Some specimens showed abdomen completely shaded with reddish brown; terga and sterna suffused with reddish brown, without longitudinal lines (Fig. 4-6).
Female Imago: Length: body 16.0mm; forewing 14.0mm; hind wing 6.9mm.
Similar to males. Legs atrophied; tibiae and tarsi thin and twisted. Posterior margin of sternum IX medially projected, deeply cleft (Fig. 3). Caudal filaments brown, becoming whitish toward apex.
[FIGURAS 1-6 OMITIR]
Variations: Length: body 16.0mm-18.7mm; fore wing 13.6mm-15.0mm; hind wing 6.9mm-8.0mm.
Type-material: Brazil, Rio de Janeiro: Macae, Rio Macae (22[grados]17'42.9" S - 41[grados]52'48.0" W), 16.iv.2009, Goncalves I.C., Jardim G.A., Santos A.P.M., Alecrim V.P. & Ferreira-Jr N. leg. One male imago (holotype; DZRJ629); same data, seven male imagos and five female imagos (DZRJ630); same data, two male imagos (DZRJ631); same data, one female imago (DZRJ632); Macae, Rio Sao Pedro (22[grados]16'37.7" S - 41[grados]52'22.8" W), 15.iv.2009, Goncalves I.C., Jardim G.A., Santos A.P.M., Alecrim V.P. & Ferreira-Jr N. leg. two female imagos (DZRJ627); Macae, Cachoei ros de Macae, Rio Macae, (22[grados]25'49.5" S - 41[grados]18'06.0" W), 05.iv.2009, Goncalves I.C., Jardim G.A., Sampaio B.H.L., Alecrim V.P., Dumas L.L. & Nessimian J.L. leg. six female imagos (DZRJ628).
Etymology: the name "macabaiba" is an allusion to the macabaiba palm tree, whose fruit is called "maca-e" a Tupi word that gave origin to the name Macae, municipality where this species is found.
Biology: Imagos were found to fly mainly between six p.m. and seven p.m., before eight p.m. the swarm were over.
According to Kluge (2007), presence or absence of certain veins cannot be considered a distinguishing generic character since such differences exist on adults only. Oligoneuria macabaiba sp. nov. has no cross veins behind RSa+iRS nor has IMP but in the hind wing several faint cross veins can be seen after CuA, corroborating Kluge's observations. Such feature appears to be species-specific since absence of IMP and cross veins after RSa+iRS was noticed on all specimens of O. macabaiba and O. itayana (according to Kluge, 2007). A phylogenetic revision of the genus is in preparation and will aid definition of the relations within the genus (F.F. Salles, pers. comm.).
Posterolateral spines on abdominal terga are described as "twisted" by Salles et al. (2007) and "crumpled" by Kluge (2007), but our specimens did not necessarily presented twisted or crumpled spines. In fact, the spines were found to be quite flexible, appearing twisted or not according to the individual. For this reason, we preferred to use the term "flexible" to better describe these spines. In O. macabaiba sp. nov., posterolateral spines of segment II are represented by small projections but the spines on other segments are even longer than those in O. amazonica whereas in O. itayana a sexual dimorphism is described, with females having smaller spines than males (Kluge 2007).
O. macabaiba sp. nov. differs from other species of the genus by a distinctive characteristic: the pair of processes between forceps insertions. Such projections are present in O. itayana, O. amazonica and Oligoneuria/ f5 = g6 sp.O5 draw by Kluge (2004) but are completely absent on O. macabaiba. In that sense, generic diagnosis should be expanded to comprise this trait.
Female sternum IX extends midposteriorly with a deep cleft, as seems to be common for the genus. In O. macabaiba sp. nov. and O. itayana these projections, as well as the abdominal posterolateral spines, appear to be longer than in O. amazonica. Male genitalia is distinctly different, with lack of projections on styliger plate and penes spines strongly divergent, oriented posterolaterally and broadly separated by two membranous lobes.
We are thankful to members of Laboratorio de Entomologia at Universidade Federal do Rio de Janeiro (UFRJ) from help on field trips and to the anonymous reviewers, for the valuable suggestions on the manuscript. This study was partially funded by CNPq and FAPERJ.
Kluge, N. 2004. The phylogenetic system of Ephemeroptera. Kluwer Academic, Dordrecht, Netherlands.
Kluge, N. 2007. Oligoneuria itayana sp. n. (Ephemeroptera: Oligoneuriidae)--a new mayfly species from Peruvian Amazonia. Russ. Entomol. J. 16: 127-137.
Salles, F.F., M.S. Baptista, E.R. Da-Silva, N. Hamada & J.E. Serrao. 2007. Redescription of the adults and description of the larvae and eggs of Oligoneurioides amazonicus Demoulin (Ephemeroptera: Oligoneuriidae). Aquat. Insect. 29: 139-149.
Ines C. Goncalves (1), Elidiomar R. Da-Silva (2), Jorge L. Nessimian (3)
(1.) Universidade Federal do Rio de Janeiro, Instituto de Biologia, Departamento de Zoologia, Laboratorio de Entomologia. Avenida Brigadeiro Trompowski, s/n, bloco A, sala 107, Ilha do Fundao, Rio de Janeiro, RJ, Brazil. CEP 21941-971, C. Postal 68044; email@example.com
(2.) Universidade Federal do Estado do Rio de Janeiro, Instituto de Biociencias, Departamento de Zoologia, Laboratorio de Insetos Aquaticos. Av. Pasteur, 458, 4o andar, Urca, Rio de Janeiro, RJ, Brasil CEP 22290-240; firstname.lastname@example.org
(3.) Universidade Federal do Rio de Janeiro, Instituto de Biologia, Departamento de Zoologia, Laboratorio de Entomologia. Avenida Brigadeiro Trompowski, s/n, bloco A, sala 107, Ilha do Fundao, Rio de Janeiro, RJ, Brazil. CEP 21941-971, C. Postal 68044; email@example.com
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|Title Annotation:||texto en ingles|
|Author:||Goncalves, Ines C.; Da-Silva, Elidiomar R.; Nessimian, Jorge L.|
|Publication:||Revista de Biologia Tropical|
|Date:||Dec 1, 2011|
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