Cryptic species of Gryllus in the light of bioacoustic (Orthoptera: Gryllidae)

O gênero Gryllus destaca-se com um grande número de espécies descritas e representa um dos mais complexos gêneros na sistemática dos Orthoptera, caracterizado por um conjunto de espécies cosmopolitas e crípticas. Este trabalho compara os sons emitidos por espécimens de Gryllus coletados no campus da UNESP em Rio Claro (SP), bem como a morfologia e morfometria das pars stridens, com o objetivo de aplicar os resultados no reconhecimento de possíveis espécies crípticas e contribuir na discussão de processos de especiação. Três grupos de grilos foram discriminados por diferenças nas pars stridens e sons de chamado, caracterizados por diferentes ritmos, freqüências e composição das notas, indicando assim, a presença de três espécies no local analisado, morfologicamente pouco distintas. Diante dos resultados, sugere-se a utilização das características da pars stridens e do som de chamado como caracteres diagnósticos imprescindíveis na taxonomia dos Gryllus.

Stridulatory file and calling song of two populations of the tropical bush cricket Eneoptera surinamensis (Orthoptera, Gryllidae, Eneopterinae)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Morphological characterization of the proventriculus of Gryllus assimilis Fabricius (Orthoptera, Gryllidae)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Autosomal rearrangement in Gryllus assimilis Fabricius, 1775 (Orthoptera, Gryllidae)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Genitalia, acoustics and chromosomes of Urogryllus toledopizai (Orthoptera: Gryllidae)

Morphological structures of male and female genitalia and the pars stridens of a population of Urogryllus toledopizai Mello (1988) as well as the karyotype of the species are illustrated. The characteristics of song signals and associated behavior are described and information on the seasonality of the species is provided. Disagreements with the results published by other authors are discussed.

Análise taxonômica de duas populações do gênero Hygronemobius por meio da ultramorfologia, morfometria, bioacústica e aspectos ecológicos (Orthoptera, Gryllidae, Nemobiinae)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Som de chamado, ultramorfologia da fileira estridulatória e morfologia do complexo fálico aplicados à taxonomia de Gryllus Linnaeus, 1758 do extremo sul do Rio Grande do Sul (Orthoptera, Gryllidae)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Caracterização e análise filogenética de espécies dos gêneros Anurogryllus, Urogryllus e Paranurogryllus (Orthoptera, Gryllidae), morfologia, citogenética, acústica, dna mitocondrial

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

A new species of Endecous Saussure, 1878 (Orthoptera, Gryllidae) from northeast Brazil with the first X(1)X(2)0 chromosomal sex system in Gryllidae

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Taxonomic studies on the Neotropical Landrevinae with description of new taxa (Orthoptera, Grylloidea, Gryllidae)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Taxonomic studies on the Neotropical Landrevinae with description of new taxa (Orthoptera, Grylloidea, Gryllidae)

The understanding of the subfamily Landrevinae has been modified by different authors since its creation. In the neotropics three genera are known to the present: Odontogryllus Saussure, 1877 (one from México, the others amazonian), Brasilodontus de Mello, 1992 with two species (from Brazilian Atlantic Forest), e Valchica de Mello, 1992 with one species (from Costa Rica). De Mello (1992) erroneously created the tribe Odontogryllini for this cluster of neotropical genera, here suppressed. In the present paper we revise and add new species to Brasilodontus and describe two monotypic genera, Xulavuna n. gen. and Yarrubura, n. gen. An identification key to the genera of neotropical Landrevinae is presented as well as one for the species of Brasilodontus. The male fore wings of Xulavuna adenoptera n. sp. is remarkable regarding its shape and its glandular condition

Composição da entomofauna da Floresta Nacional do Araripe em diferentes vegetações e estações do ano

A ocorrência de insetos tem grande significado ecológico e está relacionada com os fatores ambientais, disponibilidade de alimento e abrigo. Para avaliar a composição da entomofauna, em diferentes tipos de vegetação (Cerrado, Carrasco e Mata Úmida) e estações do ano na Floresta Nacional do Araripe, Crato, Ceará, nordeste brasileiro, foram realizadas coletas semanais na estação seca (setembro a dezembro) e chuvosa (abril a julho), por meio de armadilhas McPhail, de solo e bandejas amarelas. Os insetos da ordem Coleoptera são numerosos, na estação seca, agindo como polinizadores, fitófagos e detritívoros, além de decompositores de matéria orgânica, na estação chuvosa. Os Diptera são numerosos na estação chuvosa, quando são encontradas moscas frugívoras, decompositoras de carcaças de animais, de matéria orgânica e predadoras; os da família Calliphoridae predominam no Cerrado; da família Tachinidae, no Carrasco, e da Tephritidae, na Mata Úmida. Os Orthoptera Gryllidae predominam na Mata Úmida e os Hymenoptera Formicidae, no Carrasco e Cerrado na estação seca. Portanto, cada grupo de insetos desempenha um papel ecológico sobre as vegetações, nas diferentes estações do ano.

Comportamento do Heterocromossômio em alguns Ortópteros do Brasil

In the present paper the behavior of the heterochromoso-mes in the course of the meiotic divisions of the spermatocytes in 15 species of Orthoptera belonging to 6 different families was studied. The species treated and their respective chromosome numbers were: Phaneropteridae: Anaulacomera sp. - 1 - 2n = 30 + X, n +15+ X and 15. Anaulacomera sp. - 2 - 2n - 30 + X, n = 15+ X and 15. Stilpnochlora marginella - 2n = 30 + X, n = 15= X and 15. Scudderia sp. - 2n = 30 + X, n = 15+ X and 15. Posldippus citrifolius - 2n = 24 + X, n = 12+X and 12. Acrididae: Osmilia violacea - 2n = 22+X, n = 11 + X and 11. Tropinotus discoideus - 2n = 22+ X, n = 11 + X and 11. Leptysma dorsalis - 2n = 22 + X, n = 11-J-X and 11. Orphulella punctata - 2n = 22-f X, n = 11 + X and 11. Conocephalidae: Conocephalus sp. - 2n = 32 + X, n = 16 + X and 16. Proscopiidae: Cephalocoema zilkari - 2n = 16 + X, n = 8+ X and 8. Tetanorhynchus mendesi - 2n = 16 + X, n = 8+X and 8. Gryliidae: Gryllus assimilis - 2n = 28 + X, n = 14+X and 14. Gryllodes sp. - 2n = 20 + X, n = 10- + and 10. Phalangopsitidae: Endecous cavernicola - 2n = 18 +X, n = 94-X and 9. It was pointed out by the present writer that in the Orthoptera similarly to what he observed in the Hemiptera the heterochromosome in the heterocinetic division shows in the same individual indifferently precession, synchronism or succession. This lack of specificity is therefore pointed here as constituting the rule and not the exception as formerly beleaved by the students of this problem, since it occurs in all the species referred to in the present paper and probably also m those hitherto investigated. The variability in the behavior of the heterochromosome which can have any position with regard to the autosomes even in the same follicle is attributed to the fact that being rather a stationary body it retains in anaphase the place it had in metaphase. When this place is in the equator of the cell the heterochromosome will be left behind as soon as anaphase begins (succession). When, on the contrary, laying out of this plane as generally happens (precession) it will sooner be reached (synchronism) or passed by the autosomes (succession). Due to the less kinetic activity of the heterochromosome it does not orient itself at metaphase remaining where it stands with the kinetochore looking indifferently to any direction. At the end of anaphase and sometimes earlier the heterochromosome begins to show mitotic activities revealed by the division of its body. Then, responding to the influence of the nearer pole it moves to it being enclosed with the autosomes in the nucleus formed there. The position of the heterochromosome in the cell is explained in the following manner: It is well known that the heterochromosome of the Orthoptera is always at the periphery of the nucleus, just beneath the nuclear membrane. This position may be any in regard of the axis of the dividing cell, so that if one of the poles of the spindle comes to coincide with it, the heterochromosome will appear at this pole in the metaphasic figures. If, on the other hand, the angle formed by the axis of the spindle with the ray reaching the heterochromosome increases the latter will appear in planes farther and farther apart from the nearer pole until it finishes by being in the equatorial plane. In this way it is not difficult to understand precession, synchronism or succession. In the species in which the heterochromosome is very large as it generally happens in the Phaneropteridae, the positions corresponding to precession are much more frequent. This is due to the fact that the probabilities for the heterochromosome taking an intermediary position between the equator and the poles at the time the spindle is set up are much greater than otherwise. Moreover, standing always outside the spindle area it searches for a place exactly where this area is larger, that is, in the vicinity of the poles. If it comes to enter the spindle area, what has very little probability, it would be, in virtue of its size, propelled toward the pole by the nearing anaphasic plate. The cases of succession are justly those in which the heterochromosome taking a position parallelly to the spindle axis it can adjust its large body also in the equator or in its proximity. In the species provided with small heterochromosome (Gryllidae, Conocephalidae, Acrididae) succession is found much more frequently because here as in the Hemiptera (PIZA 1945) the heterochromosome can equally take equatorial or subequatorial positions, and, furthermore, when in the spindle area it does offer no sereous obstacle to the passage of the autosomes. The position of the heterochromosome at the periphery of the nucleus at different stages may be as I suppose, at least in part a question of density. The less colourability and the surface irregularities characteristic of this element may well correspond to a less degree of condensation which may influence passive movements. In one of the species studied here (Anaulacomera sp.- 1) included in the Phaneropteridae it was observed that the plasmosome is left motionless in the spindle as the autosomes move toward the poles. It passes to one of the secondary spermatocytes being not included in its nucleus. In the second division it again passes to one of the cells being cast off when the spermatid is being transformed into spermatozoon. Thus it is regularly found among the tails of the spermatozoa in different stages of development. In the opinion of the present writer, at least in some cases, corpuscles described as Golgi body's remanents are nothing more than discarded plasmosomes.

Ecologie trophique de deux espèces jumelles et sympatriques de chauves-souris: Myotis myotis et Myotis blythii (Chiroptera : Vespertilionidae). Premiers résultats

M. myotis and M. blythii are two sibling species of bats that live sympatrically over wide areas of the Western Palearctic region, and which often coexist intimately in their nursery roosts. According to the principle of <<limiting similarity>> this cohabitation should imply an interspecific ecological differentiation. The hypothesis of a niche separation at the trophic level is tested here. The fecal analysis of 300 droppings collected from a zone of sympatry shows a clear interspecific differentiation in diets : M. myotis eats mostly Carabidae (Coleoptera), whereas M. blythii captures essentially Tettigoniidae, Gryllidae and Acrididae (Orthoptera). Because they consume exclusively terrestrial arthropods, M. myotis and M. blythii are typical ground and/or grass gleaning bats. However, despite their narrow niches they are probably not specialized in the predation of only some definite categories of prey. The narrow diets probably reflect the high specialization of their modes of resource exploitation: M. myotis and M. blythii prey upon ground arthropods and they are likely to select for different foraging;g habitats. M. myotis probably prefers wooded feeding grounds (Carabidae) whereas M. blythii exploits herbaceous habitats (Orthoptera). The strong trophic segregation observed in sympatry between M. myotis and M. blythii shows that the interspecific competition is distinctly much weaker than the intraspecific one. This would explain the stable, intimate co-existence of these two virtual competitors.

Soil organisms associated to the weed suppressant Crotalaria juncea (fabaceae) and its importance as a refuge for natural enemies

Soil organisms play an important role in organic crops of Crotalaria juncea (Fabaceae) and are associated with the natural conservation of the environment. The present study was aimed to investigate the population of soil organisms in the organic culture of C. juncea, as well as its importance as a refuge for natural enemies. Dalbulus maidis (Hemiptera: Cicadellidae), Diabrotica sp. (Coleoptera: Chrysomelidae), Doru luteipes (Dermaptera: Forficulidae), Gryllus assimilis (Orthoptera: Gryllidae), Lagria villosa (Coleoptera: Lagriidae), Melanotus sp. (Coleoptera: Elateridae), Meloidogyne incognita (Tylenchida: Heteroderidae), Nephila clavipes (Araneae: Nephilidae), Orius insidiosus (Hemiptera: Anthocoridae), Pheidole sp. (Hymenoptera: Myrmicidae), Phyllophaga sp. (Coleoptera: Scarabeidae), Procornitermes sp. (Isoptera: Termitidae), Solenopsis sp. (Hymenoptera: Formicidae), and Utetheisa ornatrix (Lepidoptera: Arctiidae) were identified in C. juncea. The organisms that were found during a 3-month period in 144 trenches in C. juncea were pest species (84.47%) and natural enemies (15.53%) as well. Natural enemies had an average of 11.89 individuals per 1.08 m³ of soil cultivated with C. juncea. The abundance of organisms in the pod stage (5.49%) of C. juncea was lower than that in the vegetative (83.50%) and flowering (11.01%) stages. Crotalaria juncea plants can be used as part of a crop system for Integrated Pest Management.