Dinâmica populacional do camarão Sicyonia dorsalis (Crustacea: Penaeoidea) no litoral de Cananéia, sul do estado de São Paulo

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Biological control of the oriental fruit fly (Dacus dorsalis Hendel) and other fruit flies in Hawaii,

"Literature cited": p. 100-102.

Conjugated equine estrogen, raloxifene and arterial stiffness in postmenopausal women

Methods We analyzed the influence of conjugated equine estrogen (CEE) and raloxifene on arterial stiffness. Sixty-seven healthy, normotensive women 1-10 years into menopause were assigned to receive oral placebo, conjugated equine estrogen 0.625mg, or raloxifene 60mg. Arterial stiffness was evaluated by measuring the carotid-femoral and femoral-dorsalis pedis pulse wave velocity (CF PWV, FP PWV). Systolic pressure augmentation index (AI) at the carotid artery was obtained with applanation tonometry. Results Arterial stiffness was not affected by any treatment regimen: placebo (CF PWV before vs. after: 644 vs. 626 cm/s, p = 0.09; FP PWV before vs. after: 1006 vs. 1012 cm/s, p = 0.77; AI before vs. after = 30 vs. 29%, p = 0.55), CEE (CF PWV before vs. after: 642 vs. 600 cm/s, p = 0.11; FP PWV before vs. after: 952 vs. 971 cm/s, p = 0.66; AI before vs. after: 25 vs. 32%, p = 0.82), and raloxifene (CF PWV before vs. after: 636 vs. 601 cm/s, p = 0.12; FP PWV before vs. after: 964 vs. 941 cm/s, p = 0.62; AI before vs. after: 25 vs. 25%, p = 0.65). A correlation occurred between basal stiffness and the degree of reduction in indexes measured, indicating that the higher the basal stiffness, the greater the degree of reduction, particularly in the CEE group: CF PWV (r = -0.602, p = 0.001); FP PWV (r = -0.455, p = 0.022); AI (r = -0.410, p = 0.042). Conclusions Conjugated equine estrogen and raloxifene do not seem to affect arterial stiffness of healthy normotensive women less than 10 years since menopause. Reduction in arterial stiffness seems related to its basal level.

Four new species of Macropodinium (Ciliophora : Litostomatea) from Australian wallabies and pademelons

Samples of Macropodinium spp. were collected from 3 new macropodid species: from 21 of 28 (75%) black-striped wallabies (Macropus dorsalis); 10 of 11 (91%) swamp wallabies (Wallabia bicolor); and 22 of 43 (51%) Tasmanian pademelons (Thylogale billardierii). The examination of ciliate morphology by silver impregnation and scanning electron microscopy led to the redescription of the genus Macropodinium and the description of 4 new species: Ma. tricresta sp. nov. and Ma. spinosus sp. nov. from M. dorsalis; Ma. maira sp. nov. from T. billardierii; and M. bicolor sp. nov. from W. bicolor; each species was strictly host specific. Cellular orientation was reinterpreted on the basis of vestibular morphology and it is concluded that Macropodinium spp. are laterally rather than dorso-ventrally compressed. The striated groove is thus dorso-ventral rather than lateral. Oral ciliation consisted of up to three bands: an adoral band composed of oblique kineties; a vestibular band of longitudinal kineties; and a preoral band of longitudinal kineties. Somatic ciliation occurred in two longitudinal bands: a dense band composed of several parallel kineties on the left side of the dorso-ventral groove; and a sparse band composed of a single kinety on the right internal side of the dorso-ventral groove. Few structures were homologous to those of other litostome ciliates, and thus the relationship of Macropodinium to other litostomes cannot yet be clearly defined.

Trichostome ciliates from Australian marsupials. III. Megavestibulum gen. nov. (Litostomatea : Macropodiniidae)

A new macropodiniid ciliate genus, Megavestibulum, is described which is endocommensal in the stomach of macropodid marsupials. Two new species, M. morganorum and M. kuhri, are described from Macropus dorsalis and Wallabia, bicolor respectively. Megavestibulum is holotrichous, the somatic ciliation arranged into meridional, curving kineties between broad ridges. The interkinetal ridges are lined apically by thick-walled vacuoles similar to those lining the longitudinal grooves of Macropodinium. The conical vestibulum is apical and very large, occupying up to 1/3 of the cell volume. The vestibular lip appears closable and has a cleft which may allow distention of the vestibullum to ingest large food items. The vestibular ultrastructure is similar to that of Macropodinium including the presence of vestibular vacuoles and the hemispherical differentiation of the distribution of small nematodesmata. Many specimens contained ingested whole ciliates of the genera Amylovorax and Polycosta. The structure of the vestibulum suggests that Megavestibulum is adapted for life as an active predator of other stomach ciliates as well as sweeping in small particulates. The morphology of Megavestibulum suggests that it represents the plesiomorphic body plan within the family Macropodiniidae.

Trichostome ciliates from Australian marsupials. II. Polycosta gen. nov (Litostomatea : Polycostidae fam. nov.)

A new family, Polycostidae, containing one new genus, Polycosta, of ciliates endwocommensal in the stomachs of macropodid marsupials is described. Four new species, A roundi, P. turniae, A sebastopolensis and P. parma are described from Wallabia bicolor, Macropus dorsalis, Petrogale herberti and M. eugenii, respectively. Polycosta is holotrichous with slightly spiral meridional kineties arranged between broad interkinetal ridges. The ultrastructure of one representative species displays the knitted together pattern of postciliary microtubules and kinetodesmata of somatic kinetids common in trichostomes and the interkinetal ridges are dominated by layers of dark bodies but lack ectoplasmic hydrogenosomes. The vestibulum is conical and its aperture appears capable of closing tightly in most species; vesibular kineties are continuations of the right somatic kineties into the vestibulum. There is a prominent phago-plasm delimited internally by a basket of nematodesmata derived from electron dense plates at the bases of kinetosomes the anterior somatic and vestibular kineties. There is a prominent cytoproct which is situated within an invagination of the cell in some species. Polycosta is similar to Amylovorax in terms of gross morphology, somatic ciliature and cortical ultrastructure. The vestibular ultrastructure, however, is more similar to that of Macropodinium. The affinities of the group are thus not clear and this unique combination of characters supports the erection of a new family.

Protótipo para o diagnóstico do estado dos vasos sanguíneos

De acordo com estatísticas recentes, as doenças cardiovasculares e as principais complicações associadas, como a Aterosclerose e a Hipertensão Arterial, constituem a principal causa de morte em todo o mundo. Verifica-se ainda uma incidência crescente na população jovem, mas ainda não existem métodos suficientemente eficazes para o diagnóstico precoce de Aterosclerose. Deste modo, o objectivo principal do presente trabalho consiste no desenvolvimento da instrumentação e de um método não-invasivo, rápido e barato, que permita caracterizar o estado dos vasos sanguíneos na sua norma e patologia. Neste trabalho propõe-se uma metodologia inovadora para a avaliação do estado dos vasos sanguíneos, baseada na análise do sinal fotopletismográfico de propagação da onda de pulso, tendo-se efectuado um estudo comparativo de dois métodos de aquisição de pulsos: Método 1, no qual se adquirem pulsos das digitais da mão e do pé; e Método 2, pelo qual se obtêm os pulsos da Radial e da “pedis dorsalis”. Os principais parâmetros analisados neste trabalho foram o Índice de Rigidez (m/s) e Índice de Reflexão (%), que depende essencialmente do tónus das artérias periféricas. Igualmente, foi determinada a Velocidade da Onda de Pulso pelo Método Gold-Standard e pelo Método de Frank, e o Índice de Função do Endotélio (%), que foi obtido recorrendo à Hiperemia Reactiva. No Capítulo 1 do presente trabalho, apresentam-se os aspectos mais importantes da Aterosclerose e os métodos de diagnóstico actualmente utilizados, bem como os fundamentos gerais da hemodinâmica e as propriedades mecânicas e fisiológicas dos vasos sanguíneos. No Capítulo 2 analisam-se os métodos não-invasivos utilizados em estudos clínicos para a medição da velocidade de propagação da onda de pulso, e também se apresenta uma nova metodologia para a caracterização do estado dos vasos sanguíneos, que consiste na análise de vários de parâmetros a partir do sinal fotopletismográfico da onda de pulso. No Capítulo 3 descreve-se a instrumentação utilizada na actividade experimental desenvolvida, assim como as principais características dos sensores para a aquisição do sinal fotopletismográfico. Destaca-se ainda a calibração efectuada, o software utilizado para o processamento das medidas experimentais, e a elaboração da rotina de aquisição de dados. Os dados experimentais, adquiridos através do método proposto para diferentes faixas etárias, estão apresentados no Capítulo 4, bem como a análise e discussão dos resultados obtidos. E finalmente, no Capítulo 5, apresentam-se as principais conclusões e as perspectivas futuras.

Produção de frutos de espécies da floresta de Várzea da Amazônia Central importantes na alimentação de Peixes

Com o objetivo de quantificar a contribuição que quatro espécies, Cassia leiandra Benth., Crescentia amazonica Ducke, Macrolobium acaciifolium (Benth.) Benth. e Vitex cymosa Bert. ex Spreng., oferecem através de seus frutos à alimentação dos peixes, foram marcados, aleatoriamente, dez indivíduos adultos destas quatro espécies da floresta de várzea na ilha da Marchantaria - Amazônia Central. O período de maior produção de frutos dá-se no período do alto nível das águas, entre janeiro e maio. A espécie Cassia leiandra apresentou a maior produção com 1.836 kg/ha e amplo consumo pela população local. Os principais peixes consumidores de frutos são tambaqui (Colossoma macropomum), matrinxã (Brycon cephalus), pirapitinga (Piaractus brachypomus), pirarara, (Phractocephalus hemioliopterus), bacu (Lithodoras dorsalis, Megalodoras sp.), pacu (Mylossoma sp., Myleus sp., Metynnis sp., Mylesinus sp.) e sardinha (Triportheus elongatus). As espécies de plantas estudadas apresentam potencial de aproveitamento como fonte de alimento para peixes.

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.

Nota sôbre o comportamento do heterocromossômio em Leptysma (Acrididae)

Studying the spermatogenesis of Leptysma sp. and Leptysma dorsalis, the writer was able to observe primary spermatocytes in anaphase with the heterochromosome in precession, synchronism or succession, confirming in this way what was observed by Prof. Piza in several other species of Orthoptera.

Genetic structure of Gymnures (genus Hylomys; Erinaceidae) on continental islands of Southeast Asia: Historical effects of fragmentation

Eustatic sea level changes during Pleistocene climatic fluctuations produced several cycles of connection-isolation among continental islands of the Sunda shelf. To explore the potential effects of these fluctuations, we reconstructed a model of the vicariant events that separated these islands, based on bathymetric information. Among many possible scenarios, two opposite phylogenetic patterns of evolution were predicted for terrestrial organisms living in this region: one is based on the classical allopatric speciation mode of evolution, while the other is the outcome of a sequential dispersal colonization of the archipelago. We tested the applicability of these predictions with an analysis of sequence variation of the cytochrome b gene from several taxa of Hylomys. They were sampled throughout SE-Asia and the Sunda islands. High levels of haplotype differentiation characterize the different island taxa. Such levels of differentiation support the existence of several allopatric species, as was suggested by previous allozyme and morphological data. Also in accordance with previous results, the occurrence of two sympatric species from Sumatra is suggested by their strongly divergent haplotypes. One species, Hylomys suillus maxi, is found both on Sumatra and in Peninsular Malaysia, while the other, H. parvus, is endemic to Sumatra. Its closest relative is H. suillus dorsalis from Borneo. Phylogenetic reconstructions also demonstrate the existence of a Sundaic clade composed of all island taxa, as opposed to those from the continent. Although there is no statistical support for either proposed biogeographic model of evolution, we argue that the sequential dispersal scenario is more appropriate to describe the genetic variation found among the Hylomys taxa. However, despite strong differentiation among island haplotypes, the cladistic relationships between some island taxa could not be resolved. We argue that this is evidence of a rapid radiation, suggesting that the separation of the islands may have been perceived as a simultaneous event rather than as a succession of vicariant events. Furthermore, the estimates of divergence times between the haplotypes of these taxa suggest that this radiation may actually have predated the climatic fluctuations of the Pleistocene. Further refinement of the initial palaeogeographic models of evolution are therefore needed to account for these results.

Notas e descrições em Bisaltes Thomson, 1868 e Ptericoptus Lepeletier & Audinet-Serville, 1830 (Coleoptera, Cerambycidae, Lamiinae, Apomecynini)

The following new species are described in the subgenus Bisaltes (Bisaltes): B. (B.) picticornis sp. nov. from Bolivia; B.(B.) taua sp. nov. from Brazil (Paraná and Santa Catarina) and B. (B.) unicolor sp. nov. from Ecuador. Bisaltes (B.) pictus Breuning, 1940 is transferred to the subgenus Craspedocerus. In Ptericoptus, P. hybridus hybridus Breuning, 1939 is considered a synonym of P. acuminatus (Fabricius, 1801); P. dorsalis Audinet-Serville, 1835 previously in the synonymy of P. acuminatus is revalidated and Saperda vitta Newman, 1838 is considered its synonym; P. corumbaensis sp. nov. is described from Brazil (Mato Grosso do Sul).

Revisão de Ceyxia Girault, stat. rev. (Hymenoptera, Chalcididae, Brachymeriini)

O gênero Ceyxia Girault é revalidado e 27 espécies são combinadas a ele. Sete espécies previamente descritas são diagnosticadas (ou redescritas) e discutidas, e 20 espécies novas são descritas. Ceyxia flaviscapus Girault, 1911 and C. ventrispinosa Girault, 1911 stat. rev. foram originalmente combinadas com Ceyxia e as seguintes são combinações novas: C. belfragei (Crawford, 1910) comb. nov., stat. rev.; C. concitator (Walker, 1862) comb. nov.; C. decreta (Walker, 1862) comb. nov.; C. dorsalis (Walker, 1861) comb. nov.; e C. villosa (Olivier, 1790) comb. nov. Ceyxia paraguayensis Girault, 1911 é consyiderada sinônimo júnior de Ceyxia flaviscapus Girault, 1911. As novas espécies são: C. acutigaster sp. nov.; C. amazonica sp. nov.; C. atuberculata sp. nov.; C. bellissima sp. nov.; C. dentiformis sp. nov.; C. diminuta sp. nov.; C. fusidentata sp. nov.; C. gibbosa sp. nov.; C. laminata sp. nov.; C. laticlipeata sp. nov.; C. latilabra sp. nov.; C. longiarticulata sp. nov.; C. longiscutellaris sp. nov.; C. longispina sp. nov.; C. nigropetiolata sp. nov.; C. paraensis sp. nov.; C. parvidentata sp. nov.; C. perparva sp. nov.; C. pseudovillosa sp. nov.; e C. tibiodilatata sp. nov. Dados sobre a associação com hospedeiros são apresentados para algumas espécies do gênero. Uma chave para as espécies do gênero é incluída.

Immatures of Acanthocinini (Coleoptera, Cerambycidae, Lamiinae)

Immatures of Acanthocinini (Coleoptera, Cerambycidae, Lamiinae). Larva and pupa of Eutrypanus dorsalis (Germar, 1928), collected in trunks of Pinus elliottii Engelm., and Paratenthras martinsi Monné, 1998, collected in spathes of Scheelea phalerata (Mart. ex Spreng.) Burret, are described and illustrated. Larva and pupa of Lophopoeum timbouvae Lameere, 1884, collected in Hymenaea corbaril L., Enterolobium contortisiliquum (Vell.) Morong and Pterogyne nitens Tul., are redescribed and illustrated. A table with all described immatures of Lamiinae, and a comparison among the immatures of Acanthocinini are presented. Biological notes and new records are also included.