Catalogue of type specimens of the Collection of Invertebrates of Instituto Nacional de Pesquisas da Amazônia, Manaus, Brazil. III. Hexapoda: Isoptera, Mantodea, Mecoptera, Orthoptera, Plecoptera, Trichoptera and Zoraptera

A catalogue of the type specimens of Isoptera, Mantodea, Mecoptera, Orthoptera, Plecoptera, Trichoptera, and Zoraptera deposited in the Invertebrate Collection of the Instituto Nacional de Pesquisas da Amazônia (INPA), Manaus, Brazil, is presented and updated to December, 2007. A total of eight holotypes and seven lots of paratypes of nine species of Isoptera; three holotypes and one paratype of three species of Mantodea; five holotypes and five lots of paratypes of five species of Mecoptera; eight holotypes and five lots of paratypes of eleven species of Orthoptera; three holotypes, three neotypes and two lots of paratypes of seven species of Plecoptera; six holotypes and seven lots of paratypes of ten species of Trichoptera; and two holotypes and three lots of paratypes of three species of Zoraptera, are listed. Specific names are listed alphabetically within the family, followed by bibliographic citation, original genus name, status of type, collection number, locality data and remarks when appropriate.

Variação do peso fresco em Cornops aquaticum (Bruner) (Orthoptera, Acrididae) associado a Eichhornia azurea (Sw) Kunth (Pontederiaceae) em uma baía no Pantanal de Poconé, Mato Grosso

Variação do peso fresco em Cornops aquaticum (Bruner) (Orthoptera, Acrididae) associado a Eichhornia azurea (Sw) Kunth (Pontederiaceae) em uma baía no Pantanal de Poconé, Mato Grosso. Cornops aquaticum (Bruner, 1906) (Orthoptera, Acrididae) desenvolve seu ciclo de vida sobre macrófitas aquáticas da família Pontederiaceae. Como os gafanhotos são capazes de responder às mudanças sazonais, a alternância de períodos que ocorre no Pantanal pode refletir em sua biologia. Este estudo foi desenvolvido no Pantanal de Poconé - MT, com o objetivo de avaliar possíveis variações no peso fresco dos adultos e ninfas de C. aquaticum. Durante o período de março/2006 a fevereiro/2007 coletaram-se mensalmente, 50 indivíduos de C. aquaticum. Um total de 600 indivíduos foi avaliado, sendo 43,5 % adultos e 56,5 % ninfas. Os maiores valores de peso fresco total ocorreram nos meses de setembro (9,106g; 0,182g/indivíduo) e outubro/2006 (8,865g; 0,177g/indivíduo) e os menores em março/2006 (3,413g; 0,068g/indivíduo). Nos indivíduos adultos os maiores pesos frescos foram registrados em setembro/2006 (8,680g; 0,223g/indivíduo) e outubro/2006 (8,654g; 0,234g/indivíduo), no final do período de seca, e o menor em março/2006 (1,792g; 0,138g/indivíduo), durante o período de cheia. As ninfas tiveram o maior peso fresco em abril/2006 (2,913g; 0,076g/indivíduo) início da vazante, enquanto o menor peso fresco ocorreu em outubro/2006 (0,211g; 0,016g/indivíduo) início da enchente. Apenas a variação no peso fresco médio das fêmeas foi significativa (f = 6,43; p = 0,001), com os maiores registros durante o período de enchente, o que pode evidenciar uma estratégia reprodutiva.

Longevity and fecundity of Dichroplus maculipennis (Orthoptera, Acrididae) at non-outbreaking and outbreaking situations

Dichroplus maculipennis is one of the most characteristic and damaging grasshopper species of Argentina, mainly in areas of the Pampas and Patagonia regions. We estimated and compared the longevity and fecundity of adult female D. maculipennis under controlled conditions (30ºC, 14L:10D, 40% RH) from individuals collected as last instar nymphs (VI) in the field and with a known recent history of low and high density conditions. Densities of D. maculipennis at the collecting sites were 0.95 individuals per m² in 2006 and 46 ind/m² in 2009, representing non-outbreaking and outbreaking situations, respectively. Adult female longevity in 2006 (67.96 ± 3.2 days) was significantly higher (p < 0.05) than in 2009 (37.44 ± 1.98 days). The number of egg-pods per female was 3.32 ± 0.44 for 2006 and 1.62 ± 0.26 for 2009. The average fecundity in 2006 (89.29 ± 11.9 eggs/female) was significantly greater (p < 0.05) than that in 2009 (36.27 ± 5.82 eggs/female). While it was observed that the oviposition rate was higher in 2006, this difference was not significant (p > 0.05). The fecundity curves showed that the highest values were at weeks 11 and 13 for the 2006 females, and at week 6 for those of 2009. Since the daily oviposition rate at low and high densities was not significantly different, the diminished fecundity rate at high density is attributable to their reduced longevity.

Gafanhotos (Orthoptera, Acridoidea) em áreas de cerrados e lavouras na Chapada dos Parecis, Estado de Mato Grosso, Brasil

Gafanhotos (Orthoptera, Acridoidea) em áreas de cerrados e lavouras na Chapada dos Parecis, Estado de Mato Grosso, Brasil. Foi determinada a composição e abundância de espécies de gafanhotos usando amostragem com rede entomológica durante 3 anos de estudo na Chapada dos Parecis, estado de Mato Grosso. O levantamento foi feito em áreas de lavouras e com vegetação ainda nativa (cerrados) com, respectivamente, 56 e 59 locais inventariados em cada ambiente. Foram coletados 3.031 indivíduos de gafanhotos de 64 espécies distribuídas entre as famílias e subfamílias: Acrididae (49): Gomphocerinae (21), Ommatolampinae (10), Melanoplinae (6), Acridinae (4) Leptysminae (3), Copiocerinae (3), Proctolabinae (1) e Cyrtacanthacridinae (1); Romaleidae (1): Romaleinae (13) e Ommexechidae (1): Ommexechinae (2), além de 1550 ninfas. A diversidade de espécies foi maior no cerrado (61) do que nas lavouras (16), ocorrendo o inverso com relação à abundância onde as espécies Baeacris punctulatus (Thunberg, 1824) e Orphulella punctata (De Geer, 1773) predominaram representando 49,5% do total de indivíduos coletados em toda a Chapada dos Parecis e, juntas, somam 78,8% da abundância registrada nas áreas de lavouras e tem potencial de se tornarem pragas.

Orthoptera assemblages associated with macrophytes of floodplain lakes of the Paraná River

Orthoptera assemblages associated with macrophytes of floodplain lakes of the Paraná River. The Orthoptera assemblage composition varies considerably, depending on habitat type. This study examines the spatiotemporal relationship between plant diversity, hydrometric level, environmental variables and the Orthoptera richness and abundance in floodplain lakes connected permanently or temporarily with the main channel of the Paraná River. The grasshoppers were collected fortnightly (April 2006May 2007). A total of 17 species were recorded and classified according to their frequency of occurrence in constant (7), accessory (4), or accidental (6) species. In the two lakes, the greater species richness and abundance was recorded in summer, thereby coinciding with the highest water level of the Paraná River. The most significant correlation between the orthopteran richness and abundance was with the water level. The aquatic plant richness was significantly different between the lakes, but the vegetation was dominated by Eichhornia crassipes (Mart.) Solms. (Liliales, Pontederiaceae). The lake, which was connected permanently, presented the highest values of diversity and abundance, proving to be a more diverse assemblage. The beta diversity was higher in the temporary connected lake than in the permanently connected one. The orthopterans assemblages were different between the lakes, Cornops aquaticum and Tucayaca gracilis were the species that contributed more to the level of dissimilarity. C. aquaticum was more representative in the lake temporarily connected, while T. gracilis in the permanent connected one. The water level of the Paraná River and the connectivity of the floodplain lakes play an important role to explain the abundance and richness of their orthopteran assemblages.

Sex ratios in juveniles and adults of Dichroplus maculipennis (Blanchard) and Borellia bruneri (Rehn) (Orthoptera: Acrididae)

Dichroplus maculipennis and Borellia bruneri are two of the 18 grasshopper species of actual or potential economic relevance as pests in Argentina. The objective of this study was to estimate the sex ratios for adults and older nymphs of D. maculipennis and B. bruneri in the field, and analyze possible temporal variations. The study was conducted during seven seasons (2005-06 to 2011-12) in representative plant communities of the southern Pampas region. A total of 4536 individuals of D. maculipennis, and 6038 individuals of B. bruneri were collected. The sex ratio registered in older nymphs for D. maculipennis and B. bruneri did not deviate from a 1:1 ratio (p > 0.05), suggesting that these species have such a primary sex ratio. However, a significant bias in sex composition in adults of both species was observed (p < 0.05). The sex ratio in adults of D. maculipennis was different in five of the 18 sampling dates carried out. In three sampling dates it was biased toward males, while in the other two it was biased toward females. Taking into account the sex ratio by sampling season, significant differences were recorded in two seasons. In 2007-08 the sex ratio was biased toward males (1 F:2.26 M), while in 2008-09 it was biased toward females (1.35 F:1 M). The sex ratio in adults of B. bruneri was always biased toward males (p < 0.05). We conclude that results obtained in this study indicate that various factors like differential survival, dispersion, predation, among others, could have modified the primary sex ratio in these species.

Ácidos fenólicos, flavonoides e atividade antioxidante em méis de Melipona fasciculata, M. flavolineata (Apidae, Meliponini) e Apis mellifera (Apidae, Apini) da Amazônia

Honey produced by three stingless bee species (Melipona flavolineata, M. fasciculata and Apis mellifera) from different regions of the Amazon was analyzed by separating phenolic acids and flavonoids using the HPLC technique. Data were subjected to multivariate statistical analysis (PCA, HCA and DA). Results showed the three species of honey samples could be distinguished by phenolic composition. Antioxidant activity of the honeys was determined by studying the capacity of inhibiting radicals using DPPH assay. Honeys with higher phenolic compound contents had greater antioxidant capacity and darker color.

Ocorrência do gafanhoto-do-coqueiro Eutropidacris cristata (orthoptera: acrididae) atacando plantas de eucalipto em Minas Gerais

Foram avaliados os danos causados pelo gafanhoto-do-coqueiro Eutropidacris cristata (Orthoptera: Acrididae) em plantas de eucalipto, no município de Curvelo, Minas Gerais, Brasil, em junho de 2001. As amostragens foram realizadas, contando-se o número total de plantas por linha e o de plantas atacadas por classe de desfolha de 10%, a cada dez linhas de plantio, em cinco talhões de eucalipto com sinais de ataque desse gafanhoto. Calculou-se a porcentagem de desfolha por talhão e por planta de eucalipto. A porcentagem de desfolha por planta na área atacada foi de 3,70%, variando de 0,84 a 7,93%, enquanto a de plantas atacadas por talhão foi de 4,80%, variando de 1,88 a 11,54%. Os danos causados por E. cristata não justificaram medidas de controle, mas foram feitas avaliações para acompanhar a evolução do ataque desse inseto, cujas populações reduziram-se a níveis inexpressivos após 30 dias de sua constatação nesse plantio de eucalipto.

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.

Insetos coletados durante o Projeto Maracá, Roraima, Brasil: Lista complementar.

Uma lista da isentos coletados durante o projeto Marscá é apresentada. Os seguintes táxons são listados: Neuroptera (Corydalidae, Mantispidae, Ascalaphidade, Coniopterygidae, Sisyridade, Myrmeleontidae e a Chrysopidae); Coleoptera (Cerambycidae) e Diptora (Stratymyiidae, Asilidade, Bombyliidae, Dolichopodidae., Neriidae, Tephritidae., Milichiidae, Chloropidae, Otitidae, Richardiidae., Platystomatidae, Ropalomeridae, lo chaeidae e Clusiidae). Apresenta-se também uma Lista da Orthoptera: Acridoidea (Romaleidae e Acrididae) identificados em 1983.

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.

Uma nova modalidade de sexo-determinação no grilo sul-americano eneoptera surinamensis

The male of Eneoptera surinamensis (Orthoptera-Eneopteridae) is provided with 9 chromosomes, that is, with 3 pairs of autosomes and 3 sex chromosomes. Spermatogonia. - The autosomes of the spermatogonia are of the same size and U-shaped. One of the sex chromosomes approximately equalling the autosomes in size is telocentric, while the other two are much larger and V-shaped. One of the latter is smaller than the other. The sex chromosomes as showed in Figs. 1 and 2 are designated by X, Yl and Y2, X being the larger V, Yl the smaller one and Y2 the rod-shaped. Primary spermatocytes. - Before the growth period of the spermatocytes all the three sex chromosomes are visible in a state of strong heteropycnosis. X is remarkable in this stage in having two long arms well separated by a wide commissural segment. (Figs. 4, 5 and 6). During the growth period Y2 disappears, while X and Yl remain in a condensed form until metaphase. These may be separated from one another or united in the most varied and irregular manner. (Fig. 7 to 12). In the latter case the segments in contact seem to be always different so that we cannot recognize any homology of parts in the sense os genetics. At diplotene Y2 reappears together with the autosomal tetrads. X and Yl may again be seen as separate or united elements. (Figs. 13 and 14). At later diakinesis and metaphase the three sex chromosomes are always independent from each other, Y2 being typically rod-shaped, X and Yl V-shaped, X being a little larger than Yl. (Fig. 15 to 18). At metaphase the three condensed tetrads go to the equatorial plane, while the sex chromosomes occupy any position at both sides of this plane. In almost all figures which could be perfectly analysed X appeared at one side of the autosomal plate an Yl together with Y2 far apart at the other side. (Figs. 16 and 18). Only a few exception have been found. (Figs. 17 and 19). At anaphase X goes in precession to one pole, Yl and Y2 to the other (Figs. 20 and 21). As it is suggested by the few figures in which a localization of the sex chromosomes different from the normal has been observed, the possibility of other types of segregation of these elements cannot be entirely precluded. But, if this does happen, the resulting gametes should be inviable or give inviable zygotes. Early in anaphase autosomes and sex chromosomes divide longitudinally, being maintained united only by the kinetochore. (Figs. 20 and 21). At metaphase the three sex chromosomes seem to show no special repulsion against each other, X being found in the proximity of Yl or Y2 indifferently. At anaphase, however, the evidences in hand point to a stronger repulsion between X on the one side and both Ys on the other, so that in spite of the mutual repulsion of the latter they finish by going to the same pole. Secondary spermatocytes. - At telophase of the primary spermatocytes all the chromosomes enter into distension without disappearing of view. A nuclear membrane is formed around the chromosomes. All the chromosomes excepting Y2 which has two arms, are four-branched. (Fig. 22). Soon the chromosomes enter again into contraction giving rise to the secondary metaphase plate. Secondary spermatocytes provided as expected with four and five chromosomes are abundantly found. (Figs. 23 and 24). In the former all chromosomes are X-shaped while in the latter there is one which is V-shaped. This is the rod- shaped Y2. In the anaphase of the spermatocytes with four chromosomes all the chromosomes are V-shaped, one of them (X) being much larger than the others. In those with five there is one rod-shaped chromosome (Y2). (Fig. 25), Spermatids. Two classes of spermatids are produced, one with X and other with Yl and Y2. All the autosomes as well as Y2 soon enter into solution, X remaining visible for long time in one class and Yl in the other. (Figs. 26 and 27). Since both are very alike at this stage, one cannot distinguish the two classes of spermatids. Somatic chromosomes in the famale. - In the follicular cells of the ovary 8 chromosomes were found, two of which are much larger than the rest. (Figs. 29 and 30). These are considered as being sex chromosomes. CONCLUSION: Eneoptera surinamensis has a new type of sex-determining mechanism, the male being X Yl Y2 and the female XX. The sex chromosomes segregate without entering into contact at metaphase or forming group. After a review of the other known cases of complex sex chromosome mechanism the author held that Eneoptera is the unique representative of a true determinate segregation of sex chromosomes. Y2 behaving as sex chromosome and as autosome is considered as representing an intermediary state of the evolution of the sex chromosomes.

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.

Nota sôbre cromossômios de alguns Ortópteros do Brasil

A short, report on the chromosomes of three species of Brasilian Orthoptera is given in the present paper. Meroncidius intermedins Brunner, belonging to the Pseu-dophyllidae, differs from the species already studied in the Family in having 30 instead of 34 autosomes and a metacentric sex chromosome. "Of the autosomes, 4 showed to be metacentric. The author believes that the present species may be originated from one having 34 acrocentric autosomes by means of centric fusions. The origin of ths metacentricity of the X is not discussed. Oxyprora flavicornis Redtb.,belonging to the Copiphori-dae, has spermatogonia with 29 chromosomes. Of the autosomes, 4 seemed to be metacentric. The X has the form of a V of subae-qual arms. Neoconocephálus injuscatus (Scudd.), also belonging to the Copiphoridae, is provided with secondary spermatocytes of 13 -j- X and 13 chromosomes. The heterochromosome is metacentric. In the spermatogonia, whose chromosome number has not been counted, there are a lot of metacentric elements. In the opinion of the present writer species provided with 31, 33 and 35 chromosomes should exist in the Copiphoridae.

Novos ortópteros do gênero Neoconocephalus (Tettigoniidae, Copiphorinae)

From material collected in different localities by Prof. Amilton Ferreira of the Rio Claro Faculty of Philosophy, three species of Orthoptera belonging to the family Tettigoniidae, subfamily Copiphorinae, considered new for the science were separated for being described in the present paper. These species are Neoconocephalus xiphophorus n.s. (Rio Claro, SP), Neoconocephalus precarius s.n. (Januária, MG), and Neoconocephalus rioclarensis s.n. (Rio Claro, SP). Types in the collection of the Department of Zoology of the ESALQ, Piracicaba.