Variation in length, fecundity and survival of pink wax scale, Ceroplastes rubens Maskell (Hemiptera: Coccidae), on umbrella trees

We investigated some of the factors that may lead to outbreaks of pink wax scale, Ceroplastes rubens Maskell, on umbrella trees, Schefflera actinophylla (Endl.). Estimates of birth and death rates of pink wax scale were high and variable within and among trees; variation in these rates was not related to scale density. Adult fecundity correlated significantly but weakly with adult test length; mean fecundity was 292 eggs per female with a range of 5-1178. Adult test length and its variance decreased weakly with increasing density. Field experiments showed that mortality of C. rubens is greatest during the first 24 hours after hatching when approximately half disappear. The rate of loss decreases over time with 0.3% of initial motile first-instar nymphs surviving to maturity. Rates of loss varied significantly between trees, indicating that some trees are more suitable for scale colonisation and survival.

Revision of Australian Clistoabdominalis (Diptera : Pipunculidae)

The 29 Australian species of Clistoabdominalis Skevington are revised and a phylogenetic analysis is presented. The following 23 new species are proposed: Clistoabdominalis ancylus, C. angelikae, C. capillifascis, C. carnatistylus, C. collessi, C. colophus, C. condylostylus, C. danielsi, C. dasymelus, C. digitatus, C. exallus, C. gaban, C. gremialis, C. lambkinae, C. lingulatus, C. mathiesoni, C. nutatus, C. octiparvus, C. scalenus, C. scintillatus, C. tasmanicus, C. tharra, and C. yeatesi. Pipunculus picrodes Perkins is proposed as a junior synonym of C. trochanteratus (Becker). Diagnoses and an illustrated key to species are provided. A summary of host records for all Australian species of Pipunculidae is presented to clarify confusion in the literature. Pipunculidae are documented hilltopping for the first time. This mating strategy is used by many species of Clistoabdominalis and patterns of hilltopping within the genus are examined.

Alterações fisiológicas após aplicação de silício em cacau e sua influência na preferência por pulgões

Os aspectos fisiológicos e bioquímicos influenciados pelo silício e que condicionam reações de resistência a pragas no cacaueiro ainda são pouco conhecidos. O objetivo deste experimento foi avaliar os efeitos da aplicação de silício sobre a fotossíntese, sobre o teor foliar de fenóis solúveis totais e a sua influência na preferência de Toxoptera aurantii em genótipos de cacau. O experimento foi conduzido em casa de vegetação, no delineamento de blocos casualizados, com quatro repetições, em arranjo fatorial 3 x 3, constituído por três genótipos (TSH 1188, CCN 51 e Catongo), duas doses de silicato de potássio (3 e 6 mL L-1), aplicadas por via foliar e um controle pulverizado somente com água. Foram realizadas avaliações das trocas gasosas, da fluorescência da clorofila a e do teor de compostos fenólicos foliar, além de um teste de preferência com chance de livre escolha com T. aurantii. Os genótipos TSH 1188 e CCN 51 apresentam maior eficiência fotoquímica e fotossintética, comparados com o Catongo. Independentemente do genótipo, a aplicação de silicato de potássio não alterou o índice de desempenho das plantas (PI ABS e PI TOTAL); no entanto, a dose 3 mL L-1 aumentou a fotossíntese líquida e o teor de fenóis solúveis totais. A dose 6 mL L-1 reduziu a preferência de T. aurantii pelas folhas do genótipo TSH 1188. A aplicação de silicato de potássio é promissora no aumento da resistência do cacaueiro a T. aurantii.

Biologia Centrali-Americana :zoology, botany and archaeology /edited by Frederick Ducane Godman and Osbert Salvin.

v.1 Insecta. Rhynchota. Hemiptera-Homoptera. Cicadidæ, Fulgoridæ by W.L. Distant. Supplement to th

Biologia Centrali-Americana :zoology, botany and archaeology /edited by Frederick Ducane Godman and Osbert Salvin.

v. 2, pt. 1 Insecta. Rhynchota. Hemiptera-Homoptera. Membracidæ, Cercopidæ, Tettigoniidæ, Gyponidæ

Biologia Centrali-Americana :zoology, botany and archaeology /edited by Frederick Ducane Godman and Osbert Salvin.

v. 2, pt. 2 Insecta. Rhynchota. Hemiptera-Homoptera. Aleurodidæ, Coccidæ by T.D.A. Cockerell.

Comportamento dos cromossômios na meiose de Euryophthalmus rufipennis Laporte (Hemiptera Pyrrhocoridae)

In this paper an account is given of the principal facts observer in the meiosis of Euryophthalmus rufipennis Laporte which afford some evidence in favour of the view held by the present writer in earlier publications regarding the existence of two terminal kinetochores in Hem ip ter an chromosomes as well as the transverse division of the chromosomes. Spermatogonial mitosis - From the beginning of prophase until metaphase nothing worthy of special reference was observed. At anaphase, on the contrary, the behavior of the chromosomes deserves our best attention. Indeed, the chromoso- mes, as soon as they begin to move, they show both ends pronouncedly turned toward the poles to which they are connected by chromosomal fibres. So a premature and remarkable bending of the chromosomes not yet found in any other species of Hemiptera and even of Homoptera points strongly to terminally localized kinetochores. The explanation proposed by HUGHES-SCHRADER and RIS for Nautococcus and by RIS for Tamalia, whose chromosomes first become bent late in anaphase do not apply to chromosomes which initiate anaphase movement already turned toward the corresponding pole. In the other hand, the variety of positions assumed by the anaphase chromosomes of Euryophthalmus with regard to one another speaks conclusively against the idea of diffuse spindle attachments. First meiotic division - Corresponding to the beginning of the story of the primary spermatocytes cells are found with the nucleus entirelly filled with leptonema threads. Nuclei with thin and thick threads have been considered as being in the zygotente phase. At the pachytene stage the bivalents are formed by two parallel strands clearly separated by a narrow space. The preceding phases differ in nothing from the corresponding orthodox ones, pairing being undoubtedly of the parasynaptic type. Formation of tetrads - When the nuclei coming from the diffuse stage can be again understood the chromosomes reappear as thick threads formed by two filaments intimately united except for a short median segment. Becoming progressively shorter and thicker the bivalents sometimes unite their extremities forming ring-shaped figures. Generally, however, this does not happen and the bivalents give origin to more or less condensed characteristic Hemipteran tetrads, bent at the weak median region. The lateral duplicity of the tetrads is evident. At metaphase the tetrads are still bent and are connected with both poles by their ends. The ring-shaped diakinesis tetrads open themselves out before metaphase, showing in this way that were not chiasmata that held their ends together. Anaphase proceeds as expected. If we consider the median region of the tetrads as being terminalized chiasmata, then the chromosomes are provided with a single terminal kinetochore. But this it not the case. A critical analysis of the story of the bivalents before and after the diffuse stage points to the conclusion that they are continuous throughout their whole length. Thence the chromosomes are considered as having a kinetochore at each end. Orientation - There are some evidences that Hemipteran chromosomes are connected by chiasmata. If this is true, the orientation of the tetrads may be understood in the following manner: Chiasmata being hindered to scape by the terminal kinetochores accumulate at the ends of the tetrads, where condensation begins. Repulsion at the centric ends being prevented by chiasmata the tetrads orient themselves as if they were provided with a single kinetochore at each extremity, taking a position parallelly to the spindle axis. Anaphase separation - Anaphase separation is consequently due to a transverse division of the chromosomes. Telophase and secund meiotic division - At telophase the kinetochore repeli one another following the moving apart of the centosomes, the chiasmata slip toward the acentric extremities and the chromosomes rotate in order to arrange themselves parallelly to the axis of the new spindle. Separation is therefore throughout the pairing plane. Origin of the dicentricity of the chromosomes - Dicentricity of the chromosomes is ascribed to the division of the kinetochore of the chromosomes reaching the poles followed by separation and distension of the chromatids which remain fused at the acentric ends giving thus origin to terminally dicentric iso-chromosomes. Thence, the transverse division of the chromosomes, that is, a division through a plane perpendicular to the plane of pairing, actually corresponds to a longitudinal division realized in the preceding generation. Inactive and active kinetochores - Chromosomes carrying inactive kinetochore is not capable of orientation and active anaphasic movements. The heterochromosome of Diactor bilineatus in the division of the secondary spermatocytes is justly in this case, standing without fibrilar connection with the poles anywhere in the cell, while the autosomes are moving regularly. The heterochromosome of Euryophthalmus, on the contrary, having its kinetochores perfectly active ,is correctly oriented in the plane of the equator together with the autosomes and shows terminal chromosomal connection with both poles. Being attracted with equal strength by two opposite poles it cannot decide to the one way or the other remaining motionless in the equator until some secondary causes (as for instances a slight functional difference between the kinetochores) intervene to break the state of equilibrium. When Yiothing interferes to aide the heterochromosome in choosing its way it distends itself between the autosomal plates forming a fusiform bridge which sometimes finishes by being broken. Ordinarily, however, the bulky part of the heterochromosome passes to one pole. Spindle fibers and kinetic activity of chromosomal fragments - The kinetochore is considered as the unique part of the chromosome capable of being influenced by other kinetochore or by the poles. Under such influence the kinetochore would be stimulated or activited and would elaborate a sort of impulse which would run toward the ends. In this respect the chromosome may be compared to a neüròn, the cell being represented by the kinetochore and the axon by the body of the chromosome. Due to the action of the kinetochore the entire chromosome becomes also activated for performing its kinetic function. Nothing is known at present about the nature of this activation. We can however assume that some active chemical substance like those produced by the neuron and transferred to the effector passes from the kinetochore to the body of the chromosome runing down to the ends. And, like an axon which continues to transmit an impulse after the stimulating agent has suspended its action, so may the chromosome show some residual kinetic activity even after having lost its kinetochore. This is another explanation for the kinetic behavior of acentric chromosomal fragmehs. In the orthodox monocentric chromosomes the kinetic activity is greater at the kinetochore, that is, at the place of origin of the active substance than at any other place. In chromosomes provided with a kinetochore at each end the entire body may become active enough to produce chromosomal fibers. This is probably due to a more or less uniform distribution and concentration of the active substance coming simultaneously from both extremities of the chromosome.

Sobre o comportamento mitótico e meiótico de cromossomas policêntricos ou com ponto de inserção difuso

Material: Studies were made mainly with Ascaris megalocephála Cloq. univalens and bivalens, and also with Tityus bahiensis Perty. 1) Somatic pairing of heterochromatic regions. The heterochromatic ends of the somatic chromosomes in Ascaris show a very strong tendency for unspecifical somatic pairing which may occur between parts of different chromosomes (Figs. 1, 2, 3, 7, 10, 11, 12, 13, 14, 16, 18,), between the two ends of the same chromosome either directly (Figs. 4, 5, 7, 8, 11, 12, 13, 15, 16, 17, 18) or inversely (Fig. 8, in the arrow) and also within a same chromosomal arm (Fig. 6). 2) During the early first cleavage division the chomosomes are an isodiametric cylinder (Figs. 6, 9, 11, 13, 14). But in later metaphase the ends become club shaped (Figs. 1, 2, 3, 4, 5, 7, 10) which is interpreted as the beginning of migration of chromatic substance from the central euchromatic region towards the heterochromatic regions. This migration becomes more and accentuated in anaphase (Figs. 19, 22, 23) and in the vegetative cells where euchromatic region looses more and more staing power, especially in the intersititial zones between the individual small spherical chromosomes into which the euchromatic region desintegrates. The emigrated chromatin material is finally eliminated with the heterochromatic chromosome ends (Fig. 23 and 24). 3) It seems a general rule that during mitotic anaphase all chromosomes with diffuse or multiple spindle fiber attachement (Ascaris, Tityus, Luzula, Steatococcus, Homoptera and Heteroptera in general) move to the poles in the form of an U with precedence of the chromosomal ends. In Ascaris, the heterocromatic regions are pulled passively towards the poles and only the euchromatic central portion may be U-shaped (Fig. 19, 22, 25). While in the other species this U-shape is perfect since the beginning of anaphase, giving the impression that movement towards the poles begins at both ends of a chromosome simultaneously, this is not the case in Ascaris. There the euchromatic region is at first U-shaped, passing then to form a straight or zig-zag line and becoming again U-shaped during late anaphase. This is explained by the fact that the ends of the euchromatic regions have to pull the weight of the passive heterochromatic portions. 4) While it is generally accepted that, during first meio-tic division untill second anaphase, all attachement regions remain either undivided or at least united closely, this is not the case in chromosomes with diffused or multiple attachment. Here one clearly sees in all cases so far studied four parallel chromatids at first metaphase. In Luzula and Tityus (for Tityus all figs. 26 to 31) this division is allready quite clear in paraphase (pro-metaphase) and it cannot be said wether in other species the division in sister chromatids is allready present, but not visible at this stage. During first anaphase the sister chromatids of Titbits remain more or less in contact, while in Luzula and especially in Ascaris they are quite separated. Thus one can count in late anaphase or telophase of Ascaris megalocephala bivalens, nearly allways, four separate chromosomes near each pole, or a total of eight chromatids per division figure (Figs. 35, 36, 37, 38, 39, 40, 41).

Nota sôbre Fulgora

This paper includes a few notes on some Homoptera insects of the genus Fulgora, according to a study carried out on a little collection belonging to the Laboratory of Zoology of the Escola Superior de Agricultura "Luiz de Queiroz" (Piracicaba, Brazil). The following species are mentioned: F. servillei Spinola, F. lucifera Germar, F. orthocephala (Pinto da Fonseca) and F. cearensis (Pinto da Fonseca). The types of the latter having been collected in Fortaleza (Ceará), its area of distribution is considerably enlarged by the information of its occurrence in the State of São Paulo.

Notas bionômicas e morfológicas dos pulgões que atacam as plantas cítricas

This paper deals with Toxoptera suraniii, (Boyer de Fonsc, 1841) and Aphis citricidus (Kirkaidy, 1907) (Homoptera, Aphididae ), which live on Citrus and several other plants. The second is the transmitter of the disease called "tristeza" of Citrus.

Estudos anatômicos e histológicos sôbre a subfamília Triatominae (Hetroptera, Reduviidae): III parte: pesquisas sôbre o mecanismo da picada dos Triatominae

É analisado o mecanismo da picada dos Triatominae sob a consideração das observações até hoje conhecidas em Heteroptera e Homoptera. Leva à conclusão que os dados da literatura não chegam para esclarecer o mecanismo da picada dos Triatominae. Dos resultados das pesquisas e observações do animal vivo surge o seguinte quadro: Uma contração extremamente forte do músculo protrator pode mover as mandíbulas do adulto de Triatoma infestans para frente no máximo por 500 micra. Uma fonte de alimentação suficiente pode ser encontrada na epiderme do hospedeiro (homen) apenas numa profundidade de pelo menos 1000 a 1500 micra. O lábio nem pode ser encurtado nem dobrado. Correspondendo aos "fingerfoermigen Fortsaetzen" (WEBER) encontra-se na ponta do último segmento labial um mecanismo para a fixação das mandíbulas numa certa posição. Depois do esgotamento das possibilidades de contração dos protratores das mandíbulas as últimas são fixadas na posição atual. Em seguida segue uma dilatação dos protratores e depois do relaxamento do aparelho de fixação das mandíbulas os protratores são capazes de mover novamente as mandíbulas por quasi 500 micra para frente. Êsse processo pode ser repetido umas vêzes . Com o aparelho de fixação é ligado um mecanismo para a limpeza das mandíbulas na parte apical do último segmento labial em forma de uma escova. Na cabeça dos Triatominae é situado um órgão de contrôle muito complicado para estímulos mecânicos controlando a entrada das mandíbulas no tecido do hospedeiro. (O órgão receptivo correspondente para estímulos químicos é o órgão gustativo da epifaringe, já descrito umas vêzes.) O órgão representa um prolongamento do fim do tentório tubiforme dirigindo-se para frente. Perto da alavanca de articulação das mandíbulas o tubo, cheio de um líquido, aumenta-se formando uma vesícula que se insere na alavanca citada e na parede da cabeça diretamente ou por meio de tonofibrilas. Daqui o tubo continua pela antena inteira e insere-se, fechado no fim, por dois feixes de tonofibrilas fortes na extremidade do último segmento antenal. Imediatamente antes do órgão de Johnston insere-se no tubo do órgão de contrôle um scolopídio grande com a contrainserção na parede da antena (pedicelo). Cada tensão na vesícula na alavanca de articulação da mandíbula altera a pressão no líquido do órgão. A alteração da pressão é percebida pelo scolopídio. O scolopídio possui um aparelho terminal que representa uma invaginação da cutícula da parede antenal. Esta formação encontra-se também nos scolopídios do orgão de Johnston. O órgão pertence tanto às formas hematófagas dos gêneros Triatoma e Rhodnius como também à várias formas predatoras e fitófagas. Pode-se supor que o órgão é presente num grande número dos Heteroptera e que, eventualmente, representa uma parte do plano geral da ordem. O grau da evolução muito elevada deste órgão de controle indica que tem um papel importante para a manutenção da vida das espécies.

New records about Brazilian Strepsiptera (Insecta)

Além de descereverem uma nova espécie de Halictophagidae, Halictophagus lappidae, baseados em uma fêmea encontrada parasitando um exemplar de Lappida armata Melichar, 1912 (Homoptera, Dictyopharidae) proveniente de Cachimbo, Pará, os AA. fazem a descrição das larvas do 1º estadio de Halictophagus lopesi Oliveira & Kogan, 1959, e de pseudoxenos pierci (Brèthes, 1922) (Stylopidae), as primeiras larvas de Strepsiptera descritas do Brasil.

The species of Aspona Stål and nomenclatural notes (Hemiptera, Cicadomorpha, Membracidae)

The genus Aspona Stål contains now only two species: A. bullata Stål, 1862 (= Aspona gibosa Fonseca & Diringshofen, 1969 syn. nov. = Taunaya gibbosa Remes-Lenicov, 1973 syn. nov.) and A. quadrinodosa (Fonseca & Diringshofen, 1969) comb. nov. (formerly in Cyphotes Burmeister).

The species of membracids described by C. Berg and M. Spinola classified in Sundarion Kirkaldy (Hemiptera, Cicadomorpha, Membracidae)

Pyranthe acaciae Berg, 1883 and Hemiptycha chilensis Spinola, 1852 are reinstated in Sundarion Kirkaldy, 1904 (formerly in synonymy of Callicentrus bonasia (Fabricius, 1775) (Centrotinae, Nessorhinini)). Pyranthe frustratoria Berg, 1883 (also formerly considered as synonym of Callicentrus bonasia) becomes a new synonym of Sundarion flavomarginatum (Fairmaire, 1846).

A new species of Calloconophora Dietrich (Hemiptera, Membracidae) from the semi-arid region of northeastern Brazil

A new species of treehopper, Calloconophora gaudencia sp. nov., from Araruna, Paraíba State, is described and illustrated.