100 ARTIGO Redescription of the adults and description of

A ser enviado para Aquatic Insects
100 ARTIGO
Redescription of the adults and description of the nymphs and
eggs of Oligoneurioides amazonicus Demoulin (Ephemeroptera:
Oligoneuriidae)
F. F. SALLES1, M.S. BAPTISTA1, E.R. DA-SILVA2, N. HAMADA3 & J.E. SERRÃO4
1
Museu de Entomologia, Departamento de Biologia Animal, Universidade Federal de
Viçosa, MG, Brazil,
2
Departamento de Ciências Naturais, Escola de Ciências
Biológicas, Universidade Federal do Estado do Rio de Janeiro, RJ, Brazil,
3
Coordenação de Pesquisas em Entomologia, Instituto Nacional de Pesquisas da
Amazônia, Manaus, AM, Brazil, and 4Universidade Federal de Viçosa, Departamento
de Biologia Geral, Viçosa, Minas Gerais, Brazil.
Abstract
The adults of the genus Oligoneurioides and its type-species, O. amazonicus, are
redescribed. Their nymphs are formerly described for the first time and the knowledge
regarding the distribution of the genus and the species is extended. Notes on the
biology of the nymphs are also provided. The genus can be distinguished from the other
described genus of the family by the following combination of characters: In the adults:
(1) ventral portion of head concealed by a membranous extension of the frons; (2) vein
IMP of forewings absent; (3) cross veins restricted to spaces between C and Sc, R1 and
R3; (4) hind wings without cross veins; (5) genital forceps present; (6) penis sclerotized,
apically curved; (7) apex of styliger plate with long posterolateral projections; and (8)
sternum IX of female posteromedially extended and broadly cleft. In the nymphs: (1)
Head strongly projected anteriorly; (2) mid and hind episternum and epimeron projected
laterally; (3) tarsal claws well developed, hooked and with 1 – 2 subbasal denticles; (4)
prominent posterolateral projections occur on segments II – IX; and (5) terminal
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filament about as long as cerci. In the egg: Hexagonal in shape, polar caps absent and
with surface adorned with circular rugose protuberances.
Keywords: Olgoneurioides, redescription, Neotropics, Brazil.
Correspondence: Frederico Falcão Salles, Universidade Federal de Viçosa, Museu de
Entomologia, Departamento de Biologia Animal, CEP 36570-000, Viçosa, Minas
Gerais, Brasil. Fax: +55 31 3899 2537. Email: [email protected]
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Introduction
Demoulin (1955), in a paper dealing with several mayflies (Ephemeroptera) from
southern and northern Brazil, described Oligoneurioides amazonicus Demoulin, a new
genus and species of Oligoneuriidae. The description was based on two males adults
examined by him, and two additional specimens (one male and one female adults)
formerly treated by Eaton (1883) erroneously as Oligoneuria anomala Pictet.
In the same work, Demoulin (1955) also described an historically enigmatic
nymph of Oligoneuriidae, which possesses a long dome-shaped frons extending
anteriorly. This nymph, described for the first time by Spieth (1943) as the unknown
immature stage of Oligoneuria Pictet, was assigned by Demoulin (1955) as
Spaniophlebia Eaton, another genus where nymphs remained unknown. Later, Koss &
Edmunds (1970) stated that because of the general correlation between the size of the
frons extension in nymphs and adults of oligoneuriids, these nymphs could not belong
to Spaniophlebia, once adults of this genus have a small frons. Since than, there were
no other works dealing with this nymph, and until now its identity remain unclear.
Recently, on collecting trips in several areas of Brazil’s Amazon Region,
numerous Oligoneuriidae nymphs of that type, with well projected dome-shaped frons,
were found. In the meantime, we also rediscovered adults, males and females, of O.
amazonicus. These adults, besides sharing the same abdominal color pattern as these
nymphs, have a membranous frons extension, so long that covers the ventral portion of
their heads. One dissected male mature nymph, with the genitalia of the subimago fully
developed, leave us no doubt that they belong to the same species. Therefore, the aim
of the present paper is to redescribe the adults of O. amazonicus, formally describe the
nymphs of the genus, and describe their eggs for the first time.
Material and methods
Material was preserved in 80% ethanol. Body parts of nymphs and adults were
mounted on microscope slides in euparal or glycerin and drawn with a camera lucida
attached to a stereo microscope. Eggs were extracted from a mature nymph, dehydrated
in a graded ethanol series, dried by critical point-method, and mounted on SEM stubs
and sputter coated with gold; then observed and photographed with Leo VP 1430
scanning electron microscope. Terms used in descriptions of thorax are from Kluge
(1994). Material deposition is abbreviated as follows: Invertebrate Collection of the
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Instituto Nacional de Pesquisas da Amazônia, Manaus, Brazil (INPA), InstitutoFundación Miguel Lillo, Tucúman, Argentina (IFML).
Genus Oligoneurioides Demoulin, 1955
(Figs. 1 – 26)
Oligoneurioides Demoulin, 1955: 24; Eaton, 1883-1888: 30; Spieth, 1943: 12;
Demoulin, 1955: 27; Koss & Edmunds, 1970: 64; Hubbard, 1982: 269.
Type species: Oligoneurioides amazonicus Demoulin, 1955 (original designation).
Included species: Oligoneurioides amazonicus Demoulin, 1955.
Distribution: Northern Brazil (Fig. 1).
Imago. Length of male: body 7.3 mm; forewing unknown. Length of female: body 8.8
mm; forewing 7.3 mm.
Head. Eyes widely separated on meson of head by a length approximately equal
maximum width of a eye. Antennae broken-off. Ventral portion of head concealed by a
membranous extension (Figs. 2, 3).
Thorax. Width of pronotum 0.3 times length. Mesoescutellum with short membranous
filaments.
Wings. Membrane of fore and hind wings covered with microtrichiae. Hind wings 0.7
times as long as forewings. Maximal width of forewings slightly more than 0.5 times
maximal length. Forewings (Fig. 4) with cross veins restricted to spaces between C and
Sc, R1 and R3; hind wings (Fig. 5) without cross veins; vein IMP of forewings absent;
MA of hind wings unforked.
Legs. Ratios of segments in male forelegs: 0.98: 1.00 (1.0 mm): 0.17: 0.13: 0.20;
forelegs 0.9 times the length of meso and metathoracic legs (Fig. 2); tibiae of mid and
hind legs membranous; claws blunt. Legs of females with tibiae and tarsi atrophied and
twisted, femora well developed (Fig. 3).
Abdomen. Posterolateral spines present on abdominal segments II – IX, twisted on
segments II – VII, sometimes VIII; more developed on segment IX. Male genitalia
(Fig. 6).
Width of styliger plate 1.15 times maximal length; apex with long
posterolateral projections inserted in a somewhat trapezoidal membranous base.
Forceps with segment I 10 times length of segment II; 2/3 of segment I covered
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medially with setae. Sternum VII of female without emargination nor deeply cleft;
sternum IX posteromedially extended and broadly cleft (Fig. 7). Caudal filaments.
Male: terminal filament and cerci subequal, apical 2/3 of caudal filaments with whorls
of long setae on articulations. Female: caudal filaments broken-off and lost.
Mature nymph (Fig. 8). Length of male body: 11 mm. Length of female body 12 mm.
Head.
Prognathous, strongly extended anteriorly; anterior and lateral margins of
extension covered ventrally with dense setae.
Antennae inserted in front of eyes.
Mouthparts typical of remaining oligoneuriid genera (Figs. 11-16).
Thorax. Width of pronotum 4.2 times length. Legs: foretarsi developed; forecoxae and
foretrochanters subequal in length; metatrochanters distinctly smaller than metacoxae;
meso and metatarsi 0.9 length of tibiae; tarsal claws hooked and denticulate, 1 – 2
subbasal denticles (Fig. 19). Mes and metepisternum and epimeron projected laterally.
Coxae of mid and hind legs with a ventral patch of setae (Fig. 20). Metasternum
medially with two patches of dense setae.
Abdomen. Posterolateral spines on segments II – IX, all bordered externally with long
setae. Terga and sterna with setae. Gills. Gill I ventral, tufts multibranched, lamellae
absent; gills II – VII dorsal, tufts present and branched, lamellae circular. Sternum II VI with posterior area of dense setae, this area may be separated medially on the last
segments (Figs. 21, 22). Sternum IX posteromedially extended and broadly cleft (Fig.
23). Terminal filament 5/6 as long as cerci, both with long setae throughout entire
length, except for basal 1/5, bare.
Eggs (Figs. 24 - 26). Length: 200 µm. Maximum width: 176 µm. Hexagonal, polar cap
absent. Egg surface adorned with circular rugose protuberances.
Diagnoses
This genus can be distinguished from the other genera of the family by the following
combination of characters.
In the adults: (1) ventral portion of head concealed by a membranous extension
of the frons; (2) vein IMP of forewings absent; (3) cross veins restricted to to spaces
between C and Sc, R1 and R3; (4) hind wings without cross veins; (5) genital forceps
present; (6) penis sclerotized, apically curved; (7) apex of styliger plate with long
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posterolateral projections; and (8) sternum IX of female posteromedially extended and
broadly cleft.
In the nymphs: (1) Head strongly projected anteriorly; (2) mid and
hind
episternum and epimeron projected laterally; (3) tarsal claws well developed, hooked
and denticulate, 1 – 2 subbasal denticles; (4) gill lamellae on segments II – VII circular;
(5) prominent posterolateral projections on segments II – IX; and (6) terminal filament
about as long as cerci.
In the egg: Hexagonal in shape, polar caps absent. Egg surface adorned with
circular rugose protuberances.
Oligoneurioides amazonicus Demoulin, 1955
Male imago. General coloration yellowish brown and gray.
Head. General coloration yellowish brown, with blackish band along anterior and
lateral margins, and with grayish marks on vertex; inner margin of pedicel brownish,
remaining parts of antennae whitish. Eyes black. Ocelli transparent.
Thorax. Pronotum yellowish brown suffused with gray; mesonotum yellowish brown,
anterior margin and basal 1/3 of mesoescudum, margins of submesoescudum and scutal
posterior protuberance marked with gray; metanotum pale yellow suffused with gray;
pro and metasternum transparent, mesosternum yellowish brown.
Wings. Wings with membrane light gray; longitudinal and cross veins purplish gray.
Legs. Femora yellowish brown strongly suffused with gray. Tibiae and tarsi whitish.
Abdomen. Terga grayish brown, anterior and posterior margin of segments I – VII
whitish; segments I – VIII with two pairs of spots aside midline, anterior pair darker and
surrounded with black, posterior pair light gray; segments VIII – X yellow brown
suffused with gray; posterolateral projections darker. Sterna light gray. Sterna VIII – X
yellow brown suffused with gray, posterolateral extensions of styliger plate whitish.
Forceps and caudal filaments whitish gray.
Female imago. Similar to male imago, except for: general coloration darker; tibiae
suffused with gray; wings with longitudinal and cross veins yellowish; and abdominal
coloration. In females the terga are yellowish, and besides the two pairs of spots, two
longitudinal brown bands are present on each side of midline. These longitudinal bands
are eventually connected to each other by a transversal brown band.
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Mature nymph. General coloration brown (Fig. 8).
Head. Brown, suffused with dark brown and with whitish and irregular dark brown
marks. Ocelli whitish, inner margins blackish. Eyes black. Antennae pale yellow.
Thorax. Nota brown; pronotum with a median blackish mark and a pair of lateral
brownish marks; mesonotum with a median longitudinal brown band, and irregularly
marked with dark brown. Sterna yellowish brown. Legs yellowish, femora of all legs,
especially mid and hind legs, washed with brown; tibiae of all legs yellowish, with
subbasal and apical brown transverse band; mid and hind tibiae with inner margins
brownish; tarsal claws yellowish, apically brown.
Abdomen. Color pattern of terga similar to female imago, except that the general
coloration is brown and lateral margins of all segments yellowish white.
Sterna
yellowish brown. Gills brown. Caudal filaments light brown, apically whitish.
Material examined
Brazil, Mato Grosso state, Pontes e Lacerda County, Guaporé River (15o12’S,
59o21’W), N. Hamada, 20/vii/2004, 1 nymph (INPA).
o
Roraima state, Bonfim
o
County, Raia stream (03 21’N, 59 54’’W), N. Hamada & F.F. Salles, 20/x/2004, 6
nymphs (INPA).
Caracaraí County, Rio Branco River, Cachoeira Bem-Querer
(01o55’’N, 61o00’’W), N. Hamada, 15/xii/2000, 1 nymph (IFML). Boa Vista County,
Cauamé River (03o01’N, 61o08’W), N. Hamada, 24/x/2001, 1 nymph. Maranhão
state, Carolina County, Itapecuru River, above waterfall (07o24’S, 47o12’W), N.
Hamada, 15/xi/2000, 4 nymphs (INPA); Polme road, Barrolândia, Urupuxete River, N.
Hamada, 12/viii/2001, 1 nymph (INPA); São Brás (07o03’S, 47o16’W), N. Hamada,
16/xi/2000, 4 nymphs (IFML); Marajá stream (07o11’S, 47o23’W), N. Hamada,
13/xi/2000, 4 nymphs (INPA); Itapecuru River, above the bridge (07o24’S, 47o12’W),
N. Hamada, 07/viii/2001, 1 nymph (INPA). Rondônia state, Porto Velho County,
Mutum River (above the bridge) (09o39’S, 64o56’W), N. Hamada, R.L.M. Ferreira, J.O.
Silva, 08/vi/2004, 1 nymph (IFML); Jaci-Paraná River (before the entrance of Branco
River) (09o18’S, 64o25’W), N. Hamada, R.L.M. Ferreira, J.O. Silva, 10/vi/2004, 2
nymphs (INPA); Jaci-Paraná River (after Branco River) (09o31’S, 64o21’W), N.
Hamada, R.L.M. Ferreira, J.O. Silva, N, Rondônia, 10/vi/2004, 1 nymph (INPA);
Branco River (right bank tributary of Jaci-Paraná River) (09o26’S, 64o20’W), N.
Hamada, R.L.M. Ferreira, J.O. Silva, 10/vi/2004, 4 nymphs (INPA).
Diagnosis
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As this genus remains monospecific, those characters used in the generic section should
also be used for specific diagnosis.
Biology
This species was found in a wide range of habitat in the North (Roraima, Mato
Grosso and Rondônia states) and Northeast (Maranhão state) region of Brazil. Nymphs
were collected in water courses located in areas covered with Rain forest (Mato Grosso
and Rondônia states) and Savanna (Roraima and Maranhão states) vegetation type.
Specimens collected in Savanna were collected in smaller streams, with width varying
from 2 to 20 m (n = 6), while the ones collected in the Rain forest were collected in
larger rivers, with width varying from 20 to more than 50 m (n = 5). Water temperature
varied from 20 to 20oC, pH from 5.8 to 7.8 and electrical conductivity below 10 to 30
µS/cm.
Nymphs used submerged leaves and roots from marginal vegetation as
substrate, located in areas with high water velocity.
Acknowledgements
This work was supported by Brazilian Research Agencies CNPq, CAPES and
FAPEMIG, also by INPA and Furnas Centrais Elétricas. FFS and MSB are doctoral
students at the Universidade Federal de Viçosa (UFV) and JES is a staff member of
UFV and research fellow from CNPq.
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References
Demoulin, G. 1955. Une mission biologique belge au Brésil. Éphéméroptères. Bulletin
de l'Institute Royale des Sciences Naturales de Belgique, 31(20): 1-32.
Eaton AE. 1883-1888. A revisional monograph of recent Ephemeridae or mayflies.
Transactions of the Linnean Society of London. 3: 1-352.
Hubbard MD. 1982. Catálogo abreviado de Ephemeroptera da América do Sul. Papéis
Avulsos Zool. 34: 257-282.
Koss RW; Edmunds Jr GF. 1970. A new species of Lachlania from New Mexico with
notes on the genus (Ephemeroptera: Oligoneuriidae).
Proceedings of the
Entomological Society of Washington, 72 (1): 55-65.
Kluge NJ. 2004. The phylogenetic system of Ephemeroptera. Kluwer Academic
Publishers, Dordrecht/Boston/London, 442 pp.
Spieth HT. 1943. Taxonomic studies on the Ephemeroptera. III. Some interesting
Ephemerids from Surinam and other Neotropical localities. American Museum
Novitates 1244: 1-13.
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Legends
Figure 1. Geographic distribution of O. amazonicus in Brazil.
Figures 2 – 7. Oligoneurioides amazonicus, adult. 2. Forewing. 3. Hind wing. 4.
Head and thorax of male (lateral). 5. Head and thorax of female (ventral). 6. Male
genitalia (ventral). 7. Female sternum IX (ventral).
Figure 8. Oligoneurioides amazonicus, nymph. 9. Dorsal view of nymph.
Figures 9 – 16. Oligoneurioides amazonicus, nymph. SEM photographs. 9. Head
(dorsal). 10. Detail of dorsal view of head. 11. Left mandible. 12. Detail of left
mandible, showing incisives and prostheca. 13. Maxilla. 14. Detail of galea-lacinia.
15. Labium (ventral). 16. Labium (dorsal).
Figures 17 – 26. Oligoneurioides amazonicus, nymph. SEM photographs. 17. Detail
of fore leg. 18. Detail of setae on the inner margin of fore leg. 19. Detail of hind tarsi
and claw.
20.
Detail of mid coax, showing ventral patch of dense setae.
21.
Abdominal sternites II – VII. 22. Detail of abdominal sternites IV, showing ventral
patch of dense setae. 23. IX sternit of female. 24. Eggs. 25. Eggs. 26. Detail of egg
surface.
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