Pulverização de novos acaricidas no combate ao ácaro da leprose Brevipalpus phoenicis (GEIJSKES, 1939) (Acari: Tenuipalpidae) em citros

O ácaro da leprose é, segundo alguns autores, o vetor responsável pela transmissão da leprose, doença possivelmente causada por um vírus. Este trabalho foi realizado com o objetivo de combate químico ao ácaro, que nos últimos anos está se tornando mais importante. Os tratamentos eram seis, cada um com quatro repetições, mas os produtos eram três. Cada laranjeira recebeu 3,33 litros de calda. Todos os defensivos utilizados conduziram a excelentes resultados até os 89 dias após a pulverização, ocasião em que os trabalhos foram encerrados.

Novo ensaio de combate químico ao ácaro da leprose dos citros Brevipalpus phoenicis (Geijskes, 1939) em laranjeiras

O ácaro da leprose Brevipalpus phoenicis (Geijskes, 1939) é o vetor responsável pela transmissão do agente causador da leprose em laranjeiras, possivelmente um vírus. A doença é grave, responsável por grandes perdas nos laranjais paulistas. Este trabalho foi realizado com o objetivo de combate a esse ácaro com a aplicação de defensivos químicos. Tratamentos: A) testemunha; B) fempropatrina (13,5g); C) clofentezina (20,0g); D) bifentrina (5,6g); E) binapacril (50,0g); F) flubenzimina (60,0g); G) ciexatina (20,0g). As quantidades entre parênteses sao de ingrediente ativo para 100 litros de água. Gastaram-se 4 litros de calda por árvore e 1.332 litros por hectare. A ciexatina, binapacril e bifentrina foram os tratamentos mais eficientes, principalmente a ciexatina.

Ácaro da leprose Bvevipalpus phoenicis (Geijskes, 1939): combate experimental em laranjeiras

Com o objetivo de combater o ácaro da leprose foi montado um campo experimental com os seguintes tratamentos: A) testemunha; B) clofentezina, 9,45g; C) clofentezina, 9,45g + alquenóis multimetílicos, 0,4g; D) quinometionato, 25,Og; E) quinometionato, 37,5g; F) piretróide RU-1.000, l,76g; G) piretróide RU-1.0Q0, 2,0g; H) dicofol, 37,0g (tratamento padrão). As quantidades citadas são de ingredientes ativos em 1000 litros de calda (Tabela 1). Cada laranjeira foi pulverizada com 6 litros de calda, aplicada com pulverizador costal motorizado. Foram feitas 6 avaliações: a prévia (03 dias antes da pulverização) e 5 pos-aplicaçao (05, 14, 18, 26 e 35 dias após a aplicação). Pela análise dos resultados obtidos verifica-se que os tratamentos B, F, G e H. foram os mais eficientes. Os resultados da redução real podem ser observados na Tabela 2.

Sobre algumas espécies do gênero Eustala (Araneae, Araneidae) do Brasil

Duas espécies de Eustala Simon, 1895 são descritas do Rio Grande do Sul, Brasil: Eustala belissima sp. nov. e Eustala crista sp. nov., representadas por ambos os sexos. A fêmea de E. itapocuensis Strand, 1916 e os machos de E. nasuta Mello-Leitão, 1939, E. perfida Mello-Leitão, 1947 e E. secta Mello-Leitão, 1945, são descritos pela primeira vez. Novas ocorrências do Brasil são listadas para Eustala illicita (O. P.-Cambridge, 1889) e E. sagana (Keyserling, 1893).

Anfíbios Anuros da coleção Adolpho Lutz: III - Hyla claresignata Lutz & B. Lutz, 1939

Hyla claresignata Lutz & Lutz, 1939, is a large species apparently not closely allied to the other known Brazilian hylas. It is characterized by the very small tympanum; the head is short and the snout rounded; the legs are long, the hands and feet unusually large, the latter extensively webbbed. The specific name is derived from the insular, irregular, or roughly triangular, dark spots, with a light halo, found mostly in the dorso-lateral region and on the legs. It belongs to the rain-forest fauna of the Marítime Range. The adult is a bromeliad-dweller and the tadpole rhyacophilous. DESCRIPTION. Vomerine teeth in two separate, oblique, groups, behind the large choanae, parallel to the posterior half of their inner border. Tongue entire, short, very broad and hardly free behind. Snout short, rounded, with distinct canthus rostralis and gradually sloping loreal region. Eye very large and prominent, its horizontal diameter almost equal to the distance between its anterior corner and the tip of the snout. Tympanum very small, less than one third of the diameter of the eye, but distinct, partly covered by a short, heavy ridge. Lateral fingers less than one third webbed; fourth finger slightly longer than the second, just reaching the base of the disk of the third; subarticular tubercles well developed; an angular pollex rudiment, more noticeable in the males. Toes almost completely webbed, the edge of the web inserted at the base of the disk on the third and the fifth; an inner metatarsal tubercle. Skin smooth above, granular beneath, on the throat minutely so. No dermal appendage on the hell. Habit robust, head broader than long, body rather heavy, slightly narrowed in the postaxillary region. Legs long, the tibiotarsal articulation reaching beyond the tip of the snout when adpressed. Type (female): 61 mm. (Fig. 1.) DIAGNOSIS of TADPOLE (by G. Orton). "A large specialized, mountain-stream tadpole, with wide head an elongated, flattened snout, greatly enlarged lips and high tooth formula. Eyes dorsal. Spiracle sinistral, projecting, situated far back on side. Anus dextral. Tooth formula 8/12 to 9/14 in fully grown larvae. Tail with a prominent, vertical dark band across musculature and fins; a second concentration of dark pigment near tip of tail, may or may not form a similar but narrower band. Maximum known total length: 60mm.; head and body length 25mm. (Figs. 6 e 7). For further details see Lutz & Lutz, 1939 and Lutz B. & Orton G. 1946.

Descrição da fêmea de Lutzomyia wilsoni (Damasceno e Causey, 1945) (Diptera, Psychodidae, Phlebotominae)

Os autores descrevem a fêmea de L. wilsoni (Damasceno e Causey, 1945), por eles conhecida desde 1963, porém somente agora publicada, e que é extremamente semelhante à de L. saulensis (Floch e Abonnenc, 1944), o que mostra a estreita afinidade entre as duas espécies. É, também, dada a distribuição geográfica atualmente conhecida de L. wilsoni.

Nota sobre Lutzomyia (Trichopygomyia) Dasypodogeton (Castro, 1939), com a redescrição do macho e da fêmea (Diptera: Psychodidae, Phlebotominae)

Os autores, após transcreverem a descrição original da Lutzomyia (Trichopygomyia) dasypodogeton (Castro, 1939), inicialmente publicada de maneira muito resumida em jornal não científico, redescrevem, de acordo com as normas atualmente adotadas, ambos os sexos dessa espécie, inclusive com desenhos dos elementos taxonomicamente importantes. É, também, dada uma chave para a identificação das espécies do subgênero trichopygomyia Barreto, 1952.

Some new species of Caryospora (Apicomplexa: Eimeriidae) from brazilian snakes, and a re-description of C. jararacae Carini, 1939

The mature ooxysts of six new species of Caryospora are described from the faeces of Brazilian snakes. They are differentiated from other species previously recorded from reptiles, largely on the size and shape of the oocyst and sporocyst, structure of the oocyst wall, and presence or absence of a polar body. C. paraensis n. sp., and C. carajasensis n. sp., are from the "false coral", Oxyrhopus petola digitalis; C. pseustesi n. sp., from the "egg-eater", Pseustes sulphureus sulphureus; C. epicratesi n. sp., from the "red boa", Epicrates cenchria cenchria; and C. micruri n. sp., and C. constancieae n. sp., from the "coral snake", Micrurus spixii spixii. A re-description is given of C. jararacae Carini, 1939, from the "jararaca" Bothrops atrox, embodying some additional morphological features.

Estudo comparativo da genitália externa masculina de Triatoma neotomae Neiva, 1911 e Triatoma nitida Usinger, 1939 (Hemiptera, Reduviidae)

The morphological comparative study of the phallus organs, of both species, shown five structures wich may be used as taxonomic characters. They are: parameres (Pa), median process pygophore (PrP), basal plate (EPbi), gonopore (PrG) and endosoma process (PrEn).

Biologia do Triatoma nitida Usinger, 1939 em laboratório (Hemiptera: Reduviidae)

Triatoma nitida is a wild species occurring in Mexico and Central America. In order to establish the length of its life cycle and transmission potential, the following parameters were observed: the incubation period, the interval between hatching, or moulting, and the first feeding; the number of blood meals and the time of development. The time-lapse before the bite, the length of feeding and the interval between the end of the blood meal and defecation, as well as the site of defecation were also analyzed. Average length of the egg incubation period was 18.2 days. Time interval between the food source offering and the bite was less than 4 min in 60//of the analyzed cases, except in the fifth instar, where only 38//of the insects began feeding in less than 5 min. The blood-sucking period was long and rising until the fifth instar, decreasing in adults, and ranging from 1 min to 2 and a half hours. Only 26//of the blood meals were followed by defecations within 20 min. The average length of the life cycle was 897.5 days.

Variation between geographical populations of Lutzomyia (Nyssomyia) whitmani (Antunes & Coutinho, 1939) sensu lato (Diptera:Psychodidae:Phlebotominae) in Brazil

Phylogenetic analysis of morphometric and biological characters indicated that there are two distinct forms of Lutzomyia whitmani in Brazil: one is present both north and south of the River Amazonas in the State of Pará while the other occurs in northeast Brazil, in the State of Ceará, and further south, including the type locality in State of Bahia. The Amazonian form is reportedly neither strongly anthropophilic nor synanthropic, and it is the vector of Leishmania shawi; whereas the southern form is often collected peridomestically, while biting man, and has been found infected with Le.(V.) braziliensis. The ratio of the length of the genital filaments to that the genital pump was found to be consistently smaller in males of the Amazonian populations. A middle repetitive DNA element was isolated by differentially screening a genomic library made using Amazonian material, and the sequence was diagnostic for this form of Lu. whitmani (being absent or occurring in low copy number in the southern form). The total evidence suggests there are at least two, geographically-isolated forms of Lu. whitmani, which may represent different cryptic species.