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Neotrop. Entomol. vol.33 no.3 Londrina May/June 2004
SYSTEMATICS, MORPHOLOGY AND PHYSIOLOGY
Morphological characters and karyology of Miogryllus piracicabensis Piza (Orthoptera: Gryllidae)
Caracteres morfológicos e cariologia de Miogryllus piracicabensis Piza (Orthoptera: Gryllidae)
Alejo Mesa; Paula García-Novo; Thaisa Roat; Cauré Portugal
Depto. Biologia, Inst. Biociências, Universidade Estadual Paulista,Av. 24-A, 1515, Bela Vista, 13506-900, Rio Claro, SP
The genus Miogryllus includes a considerable number of species, most of them still undescribed. From those already described, the amount of afforded details on morphology is not always enough to recognize the species, missing information on phallic and pars stridens structures as well as karyology. The present paper aims to improve these information, on the species M. piracicabensis.
Key words: Gryllinae, phallic sclerites, par stridens, proventiculus structure, cytogenetics
O gênero Miogryllus inclui um número considerável de espécies, sendo que a maioria delas ainda não está descrita. A quantidade de detalhes morfológicos sobre as espécies conhecidas nem sempre é suficiente para seu reconhecimento, faltando dados sobre as estruturas fálicas e da pars stridens, bem como aqueles referentes à cariologia. O presente trabalho tem o propósito de suprir tal situação para o caso de M. piracicabensis.
Palavras-chave: Gryllinae, citogenética, esclerito fálico, par stridens, proventículo
Ten species of the genus Miogryllus Saussure, 1877 are listed by Otte et al. (2001), who included te genus in the tribe Sciobiini. Two of them are from África (M. argiropterus Rochebrune, 1934 and M. nemobioides Chopard, 1936) one from Central America (M. ensifer Scudder, 1896) one from North America (M. lineatus Scudder, 1896) and six from South America (M. bohlsii Giglio-Tos, 1895, M. convolutus Johannson, 1763, M. incertus Giglio-Tos, 1894, M. piracicabensis Piza, 1960, M. tucumanensis Giglio-Tos, 1894 and M. verticalis Serville, 1839), with M. convolutus and M. verticalis being also represented in North America.
The large number of synonyms listed by some of its species (eight for M. convolutus, three for M. lineatus and ten for M. verticalis) illustrate the present confuse stage in the taxonomy of the genus. The main reasons for that are the high variability between Miogryllus species, the wide geographical distribution and the unsuitable descriptions of some species, with no accurate morphological (mainly genitalia) as well as karyological and bioacustical references.
The present paper aims to add more detailed information about one species identified as M. piracicabensis after comparing the specimens here studied (Fig. 1) with the Piza's male and female types deposited in the insect collection of the Zoology Department of the Escola de Agricultura Luiz de Queiroz (ESALQ) in São Paulo State, Brazil.
Our specimens were collected at little more than 30 km from the type specimens locality.
Material and Methods
Specimens of M. piracicabensis were collected at Floresta Estadual "Edmundo Navarro de Andrade", during day time, hidden under stones or rotten logs. The geographic coordinates are: 22º24'48"S 47º31'29"W.
Meiotic stages were studied in male testes fixed in Carnoy I followed by acetic acid 40% treatment during few minutes to separate the cells. Suspension was then centrifugated and the supernatant medium discarded for post fixing of the remnant in Carnoy I. The centrifugation and change of fixative was repeated three times and finally the suspended cells were dropped in a hot slide until drying. The staining was done with 1% lacto-acetic orcein.
The pars stridens and proventriculus were removed, submitted to critical point Balzers CPD 050, and glued to stubs, covered with gold and examined under the scanning electron microscope Zeiss DSM 900.
The collecting date and number of specimens obtained are as follows: V-98 2, , 3 and 1 nymph; 22-VI-98, 2 ; 9-III-99, 1 nymph and one ; 11-III-99, 1 ; 22-IV-99, 3 and 3 ; 16-V-99, 3 , 2 ; 6-V-2000, 1 , 1 ; 18-X-2000, 1 ; 10-II-2001, 1 nymph; 8-IV-2001, 1 , 2 .
Measurements. Measurements of seven morphological characters of 11 males and 15 females are provided in Table 1.
Male Phallic Sclerites and Spermatophore. PECS are present as two parallel independent bars (Fig. 2a). DECS form a single "H" shaped dorso lateral sclerite. Two rear lateral projections are furnished with bristles. The rear border has a thin triangular projection in the middle line and the frontal border has two lateral projections. PECS and DECS are connected by fibrous tissue as shown in Fig. 2c. PENS is a single sclerite shaped as shown in Fig. 2a, b, c. DENS are represented by two independent sclerites nearly touching in the middle line. Each sclerite is formed by a lateral and mesal lobe connected to form a single sclerite (Fig. 2b). Its lateral lobes are connected to PENS by fibrilar tissue, as shown in Fig. 2a, b, c.
Stylet is a thin elongate sclerite placed at the dorsal side of the spermatophoric chamber (Fig. 2c). At its fore ends it has an apodeme for muscle attachment (Fig. 2c). Lateral and rear views of the spermatophore are shown in Fig. 2d and 2e respectively.
The spermatophoric chamber is quite large (Fig. 2c).
Pars stridens. The number of teeth is 84.73 ± 4.02 (n = 11) distributed along 1.5 mm. The inner end teeth of the file turn to small rounded structures (Fig. 3b).
Proventriculus Structure (Fig. 3c and d). Five is the most common number of denticles found in median teeth. Denticles of lateral teeth are more numerous and also variable in number. At the side of the lateral teeth, near its base, a bunch of setae are observed (Fig. 3c, indicated by black arrow).
Karyology. The chromosome number is 2n = = 25; = 26, with an X0 (male) XX (female) sex determining mechanism.The X is metacentric (does not appear as such in the first metaphase (Fig. 4a) but it was observed clearly metacentric in many other first metaphases). At least three autosomal pairs seem to be formed by metacentric cromossomes (see arrows) as observed in the first metaphase of Fig. 4c. During diplotene and diakinesis stages the X chromosome is not strongly heterochromatic and by this reason it is difficult to recognize (Fig. 4 a, b). C-metaphases were obtained but the quality of the few nuclei photographed did not allow to mount a reasonable good karyogram.
Piza's 1960 description of M. piracicabensis includes morphological measurements of only two specimens (one male and one female). Both male and female types have well developed wings. None of the 26 adult specimens (11 males and 15 females) collected in Rio Claro have developed wings, but the presence of wings are eventual in many species and sometimes discarded after dispersal flights. Piza's description does not provide information on male genitalia, pars stridens, proventriculus structures or chromosomes.
The only revision of the genus Miogryllus was published by Hebard (1915) and it deals mainly with North American species - few of them present in the Neotropical region - including measurements of external morphological characters of some species.
Many specimens of the genus Miogryllus from São Paulo, Minas Gerais, Paraná and Santa Catarina states are kept in the Biology Dept. collection of Univ. Estadual Paulista (Rio Claro - SP). Identification of this material will, however, need to wait until future chromosomal and bioacustical information are available. No calling song was observed and only very low mating songs were registered when female and males were kept together.
Our gratitude to Dr. Elliot W. Kitajima from the Núcleo de Apoio à Pesquisa, em Microscopia Eletrônica Aplicada à Pesquisa Agropecuária (NAP / MEPA), ESALQ (Escola de Agricultura Luis de Queiroz), USP. who furnished technical assistance and allowed to use the Scanning Electron Microscopy.
Hebard, M. 1915. The american species of the genus Miogryllus (Orthoptera, Gryllidae). J. New York Entomol. Soc. 23: 101-121. [ Links ]
Piza Jr, S.T. 1960. Três novos grilos brasileiros (Orthoptera). Studia Entomol. 3: 253-56. [ Links ]
Saussure, H. 1877. Melanges orthopterologiques V: Gryllides. Mem. Soc Phys. d'Hist. Nat. Geneve 25: 194. [ Links ]
Received 30/06/03. Accepted 10/04/04.