The black flies (Diptera: Simuliidae) from Santa Catarina, Brazil

The Simuliidae fauna from the Santa Catarina state, Brazil, was documented, based primarily on specimens deposited in the collections of the Instituto Oswaldo Cruz, Brazil and the La Plata Museum, Argentina. The results of our survey are organized by mesoregion and by municipality. Of the 51 municipalities where black flies were recorded, 46 represented new unpublished locality records. A total of 29 species belonging to two genera and eight subgenera were found, among which five are new records for the Santa Catarina state. The species recorded are (new records are marked with a *): Lutzsimulium hirticosta, Simuliium (Chirostilbia) acarayense, S. (Chirostilbia) distinctum, S. (Chirostilbia) empascae, S. (Chirostilbia) pertinax, S. (Chirostilbia) riograndense, S. (Chirostilbia) subpallidum, S. (Ectemnaspis) dinellii, S. (Ectemnaspis) lutzianum, S. (Ectemnaspis) perflavum, S. (Hemicnetha) rubrithorax, S. (Inaequalium) botulibranchium, S. (Inaequalium) clavibranchium, S. (Inaequalium) inaequale, S. (Inaequalium) itaunense, S. (Inaequalium) nogueirai, S. (Inaequalium) subclavibranchium, S. (Inaequalium) subnigrum, S. (Inaequalium) travassosi, S. (Notolepria) paraguayense*, S. (Psaroniocompsa) anamariae*, S. (Psaroniocompsa) angrense, S. (Psaroniocompsa) auripellitum, S. (Psaroniocompsa) auristriatum*, S. (Psaroniocompsa) incrustatum, S. (Psaroniocompsa) jujuyense, S. (Psaroniocompsa) limbatum*, S. (Psaroniocompsa) minuanum*, and S. (Thyrsopelma) orbitale.

The black flies (Diptera: Simuliidae) from Santa Catarina, Brazil

The Simuliidae fauna from the Santa Catarina state, Brazil, was documented, based primarily on specimens deposited in the collections of the Instituto Oswaldo Cruz, Brazil and the La Plata Museum, Argentina. The results of our survey are organized by mesoregion and by municipality. Of the 51 municipalities where black flies were recorded, 46 represented new unpublished locality records. A total of 29 species belonging to two genera and eight subgenera were found, among which five are new records for the Santa Catarina state. The species recorded are (new records are marked with a *): Lutzsimulium hirticosta, Simuliium (Chirostilbia) acarayense, S. (Chirostilbia) distinctum, S. (Chirostilbia) empascae, S. (Chirostilbia) pertinax, S. (Chirostilbia) riograndense, S. (Chirostilbia) subpallidum, S. (Ectemnaspis) dinellii, S. (Ectemnaspis) lutzianum, S. (Ectemnaspis) perflavum, S. (Hemicnetha) rubrithorax, S. (Inaequalium) botulibranchium, S. (Inaequalium) clavibranchium, S. (Inaequalium) inaequale, S. (Inaequalium) itaunense, S. (Inaequalium) nogueirai, S. (Inaequalium) subclavibranchium, S. (Inaequalium) subnigrum, S. (Inaequalium) travassosi, S. (Notolepria) paraguayense*, S. (Psaroniocompsa) anamariae*, S. (Psaroniocompsa) angrense, S. (Psaroniocompsa) auripellitum, S. (Psaroniocompsa) auristriatum*, S. (Psaroniocompsa) incrustatum, S. (Psaroniocompsa) jujuyense, S. (Psaroniocompsa) limbatum*, S. (Psaroniocompsa) minuanum*, and S. (Thyrsopelma) orbitale.

The black flies (Diptera: Simuliidae) from Santa Catarina, Brazil

The Simuliidae fauna from the Santa Catarina state, Brazil, was documented, based primarily on specimens deposited in the collections of the Instituto Oswaldo Cruz, Brazil and the La Plata Museum, Argentina. The results of our survey are organized by mesoregion and by municipality. Of the 51 municipalities where black flies were recorded, 46 represented new unpublished locality records. A total of 29 species belonging to two genera and eight subgenera were found, among which five are new records for the Santa Catarina state. The species recorded are (new records are marked with a *): Lutzsimulium hirticosta, Simuliium (Chirostilbia) acarayense, S. (Chirostilbia) distinctum, S. (Chirostilbia) empascae, S. (Chirostilbia) pertinax, S. (Chirostilbia) riograndense, S. (Chirostilbia) subpallidum, S. (Ectemnaspis) dinellii, S. (Ectemnaspis) lutzianum, S. (Ectemnaspis) perflavum, S. (Hemicnetha) rubrithorax, S. (Inaequalium) botulibranchium, S. (Inaequalium) clavibranchium, S. (Inaequalium) inaequale, S. (Inaequalium) itaunense, S. (Inaequalium) nogueirai, S. (Inaequalium) subclavibranchium, S. (Inaequalium) subnigrum, S. (Inaequalium) travassosi, S. (Notolepria) paraguayense*, S. (Psaroniocompsa) anamariae*, S. (Psaroniocompsa) angrense, S. (Psaroniocompsa) auripellitum, S. (Psaroniocompsa) auristriatum*, S. (Psaroniocompsa) incrustatum, S. (Psaroniocompsa) jujuyense, S. (Psaroniocompsa) limbatum*, S. (Psaroniocompsa) minuanum*, and S. (Thyrsopelma) orbitale.

Morfologia externa dos estágios imaturos de heliconíneos neotropicais: V. Agraulis vanillae maculosa (Lepidoptera, Nymphalidae, Heliconiinae)

The external features of egg, larva and pupa of Agraulis vanillae maculosa (Stichel, [1908]) are described and illustrated, based upon light and scanning electron microscopy.

As estruturas externas do ovo, larva e pupa de Agraulis vanillae maculosa (Stichel, [1908]) são descritas e ilustradas, baseadas em microscopia óptica e eletrônica de varredura.

Morfologia externa dos estágios imaturos de heliconíneos neotropicais: V. Agraulis vanillae maculosa (Lepidoptera, Nymphalidae, Heliconiinae)

The external features of egg, larva and pupa of Agraulis vanillae maculosa (Stichel, [1908]) are described and illustrated, based upon light and scanning electron microscopy.

As estruturas externas do ovo, larva e pupa de Agraulis vanillae maculosa (Stichel, [1908]) são descritas e ilustradas, baseadas em microscopia óptica e eletrônica de varredura.

O estágio de ovo dos Heliconiini (Lepidoptera, Nymphalidae) do Rio Grande do Sul, Brasil

Based upon light and scanning electron microscopy, the external morphology of the egg stage is described and illustrated for the following Heliconiini (Lepidoptera, Nymphalidae) from Rio Grande do Sul State, Brazil: Agraulis vanillae maculosa (Stichel, 1907), Dione juno juno (Cramer, 1779), Dione moneta moneta Hübner, 1825, Dryadula phaetusa (Linnaeus, 1758), Dryas iulia alcionea (Cramer, 1779), Philaethria wernickei (Röber, 1906), Eueides isabella dianasa (Hübner, 1806), Eueides aliphera aliphera (Godart, 1819), Heliconius ethilla narcaea Godart, 1819, Heliconius besckei Ménétriés, 1857, and Heliconius erato phyllis (Fabricius, 1775). A dichotomic key is provided for their identification, based upon differences at the levels of generic and ultrastructural morphology, and variation in host-plant use.

Utilizando-se da microscopia de luz e de varredura, são descritos e ilustrados os ovos dos seguintes Heliconiini (Lepidoptera, Nymphalidae) do Rio Grande do Sul (Brasil): Agraulis vanillae maculosa (Stichel, 1907), Dione juno juno (Cramer, 1779), Dione moneta moneta Hübner, 1825, Dryadula phaetusa (Linnaeus, 1758), Dryas iulia alcionea (Cramer, 1779), Philaethria wernickei (Röber, 1906), Eueides isabella dianasa (Hübner, 1806), Eueides aliphera aliphera (Godart, 1819), Heliconius ethilla narcaea Godart, 1819, Heliconius besckei Ménétriés, 1857 e Heliconius erato phyllis (Fabricius, 1775). Com base em diferenças morfológicas genéricas e ultraestruturais, associadas aos padrões de uso das plantas hospedeiras, elaborou-se uma chave dicotômica para a identificação das espécies.

O estágio de ovo dos Heliconiini (Lepidoptera, Nymphalidae) do Rio Grande do Sul, Brasil

Based upon light and scanning electron microscopy, the external morphology of the egg stage is described and illustrated for the following Heliconiini (Lepidoptera, Nymphalidae) from Rio Grande do Sul State, Brazil: Agraulis vanillae maculosa (Stichel, 1907), Dione juno juno (Cramer, 1779), Dione moneta moneta Hübner, 1825, Dryadula phaetusa (Linnaeus, 1758), Dryas iulia alcionea (Cramer, 1779), Philaethria wernickei (Röber, 1906), Eueides isabella dianasa (Hübner, 1806), Eueides aliphera aliphera (Godart, 1819), Heliconius ethilla narcaea Godart, 1819, Heliconius besckei Ménétriés, 1857, and Heliconius erato phyllis (Fabricius, 1775). A dichotomic key is provided for their identification, based upon differences at the levels of generic and ultrastructural morphology, and variation in host-plant use.

Utilizando-se da microscopia de luz e de varredura, são descritos e ilustrados os ovos dos seguintes Heliconiini (Lepidoptera, Nymphalidae) do Rio Grande do Sul (Brasil): Agraulis vanillae maculosa (Stichel, 1907), Dione juno juno (Cramer, 1779), Dione moneta moneta Hübner, 1825, Dryadula phaetusa (Linnaeus, 1758), Dryas iulia alcionea (Cramer, 1779), Philaethria wernickei (Röber, 1906), Eueides isabella dianasa (Hübner, 1806), Eueides aliphera aliphera (Godart, 1819), Heliconius ethilla narcaea Godart, 1819, Heliconius besckei Ménétriés, 1857 e Heliconius erato phyllis (Fabricius, 1775). Com base em diferenças morfológicas genéricas e ultraestruturais, associadas aos padrões de uso das plantas hospedeiras, elaborou-se uma chave dicotômica para a identificação das espécies.

Morfologia externa dos estágios imaturos de heliconíneos neotropicais: IV. Dryas iulia alcionea (Lepidoptera, Nymphalidae, Heliconiinae)

The external features of egg, larva and pupa of Dryas iulia alcionea (Cramer, 1779) are described and illustrated.

Morfologia externa dos estágios imaturos de heliconíneos neotropicais: IV. Dryas iulia alcionea (Lepidoptera, Nymphalidae, Heliconiinae)

The external features of egg, larva and pupa of Dryas iulia alcionea (Cramer, 1779) are described and illustrated.

Leaf selection and daily variation on feeding and oviposition of Gratiana spadicea (Klug) (Coleoptera, Chrysomelidae, Cassidinae)

Gratiana spadicea(Klug) (Coleoptera, Chrysomelidae) is a monophagous beetle that feeds only on leaves of Solanum sisymbriifolium Lamarck (Solanaceae). We determined the portions of S. sisymbriifolium leaves that are used by the adults as feeding and oviposition sites. Daily variation on larval and adult feeding frequency, and on oviposition, was also registered under laboratory conditions (25oC; 70+10% rh). Larvae and adults were fed with S. sisymbriifolium leaves during photo (14 hours) and scotophase (10 hours). At the end of each phase, it was measured the leaf area they ate and registered position of their feeding marks on leaves. The oothecae were counted and noted, regarding their position on the leaf blade. Larvae and adults of G. spadicea showed feeding activity during photo and scotophase. Oviposition was restricted to photophase. Females leaf consumption rates were greater than those of the males. Adult feeding marks were most frequent on leaf margins. Oothecae were most frequently found near the central vein of the abaxial leaf surface. Daily ingestion rates grew exponentially through the larval stage; fifth instar ingested more than 60% of the total amount of food consumed by the larval stage. The possible adaptive mechanisms involved in such feeding and oviposition patterns are discussed.

Leaf selection and daily variation on feeding and oviposition of Gratiana spadicea (Klug) (Coleoptera, Chrysomelidae, Cassidinae)

Gratiana spadicea(Klug) (Coleoptera, Chrysomelidae) is a monophagous beetle that feeds only on leaves of Solanum sisymbriifolium Lamarck (Solanaceae). We determined the portions of S. sisymbriifolium leaves that are used by the adults as feeding and oviposition sites. Daily variation on larval and adult feeding frequency, and on oviposition, was also registered under laboratory conditions (25oC; 70+10% rh). Larvae and adults were fed with S. sisymbriifolium leaves during photo (14 hours) and scotophase (10 hours). At the end of each phase, it was measured the leaf area they ate and registered position of their feeding marks on leaves. The oothecae were counted and noted, regarding their position on the leaf blade. Larvae and adults of G. spadicea showed feeding activity during photo and scotophase. Oviposition was restricted to photophase. Females leaf consumption rates were greater than those of the males. Adult feeding marks were most frequent on leaf margins. Oothecae were most frequently found near the central vein of the abaxial leaf surface. Daily ingestion rates grew exponentially through the larval stage; fifth instar ingested more than 60% of the total amount of food consumed by the larval stage. The possible adaptive mechanisms involved in such feeding and oviposition patterns are discussed.

Oviposition by the riceinfesting weevil, Oryzophagus oryzae (Costa Lima, 1936) (Coleoptera, Curculionidae): influence of water depth and host-plant characteristics

Following characterization of the egg-laying site, oviposition site selection by the rice-infesting weevil Oryzophagus oryzae (Costa Lima, 1936) (Coleoptera, Curculionidae) was studied in relation to water depth, age and density of rice in outdoor tanks. Experimental units consisted of plastic pots that were filled with different soil amounts to obtain the desired water depths in the tanks. Most eggs were laid in the submerged portions of the leaf sheath within the leaves internal air space (aerenchyma). Oviposition rates increased linearly from 10.9 to 54.5 eggs per plant with an increase in water depth from 0 to 12 cm. There was a significant interaction between water depth and host plant age, and tiller density. In water varying from 4 to 12 cm deep, females oviposited significantly more eggs on 60-day old plants (average > 75 eggs per plant) than on 15-day old plants (average 30 eggs per plant). Oviposition was negligible on 105 and 150-day old plants. Oviposition rates increased with tiller density in the 4-12 cm water depth interval. The dataindicate that females oviposit preferentially on tillering rice plants in relatively deep water, and that egg density is directly related to the number of tillers per plant.

Oviposition by the riceinfesting weevil, Oryzophagus oryzae (Costa Lima, 1936) (Coleoptera, Curculionidae): influence of water depth and host-plant characteristics

Following characterization of the egg-laying site, oviposition site selection by the rice-infesting weevil Oryzophagus oryzae (Costa Lima, 1936) (Coleoptera, Curculionidae) was studied in relation to water depth, age and density of rice in outdoor tanks. Experimental units consisted of plastic pots that were filled with different soil amounts to obtain the desired water depths in the tanks. Most eggs were laid in the submerged portions of the leaf sheath within the leaves internal air space (aerenchyma). Oviposition rates increased linearly from 10.9 to 54.5 eggs per plant with an increase in water depth from 0 to 12 cm. There was a significant interaction between water depth and host plant age, and tiller density. In water varying from 4 to 12 cm deep, females oviposited significantly more eggs on 60-day old plants (average > 75 eggs per plant) than on 15-day old plants (average 30 eggs per plant). Oviposition was negligible on 105 and 150-day old plants. Oviposition rates increased with tiller density in the 4-12 cm water depth interval. The dataindicate that females oviposit preferentially on tillering rice plants in relatively deep water, and that egg density is directly related to the number of tillers per plant.

Estrutura floral das angiospermas usadas por Heliconius erato phyllis (Lepidoptera, Nymphalidae) no Rio Grande do Sul, Brasil

A field survey of flowering plants used as food resource by the adults of Heliconius erato phyllis (Fabricius, 1775) was carried out in four sites located in Rio Grande do Sul state, Brazil. Samples were taken in preserved areas of the Atlantic Rain and Myrtaceae forests, an Eucalyptus plantation, and an urban park. Adult feeding frequencies on flowers were registered monthly from December 1996 to May 1997, on plants located on previously marked 200 m long transects. Flowers on which H. erato phyllis fed in the field were collected, drawn and morphometrically characterized. Feeding was registered on flowers of twenty-three species, of which seventeen are new records for H. erato in Brazil . The use of a given plant varied among localities, as a function of its corresponding abundance. The most visited flowers were those of Lantana camara L. and Stachytarpheta cayennensis (Rich.) Vahl, followed by Dahliapinnata Voss in the urban site. The data suggest the existence of size and shape convergence between the proboscis and the small, tubular flowers upon which H. eratophyllis feeds. They also indicate that H. eratophyllis adults have an opportunistic nectar feeding / pollen gathering habit, using several of those flowers available in a given time and locality that fit such a morphometrical pattern. Since plant species of both primitive and derived families are used, there is no indication that phylogenetic constraints play a major role in this association, nor that color of flowers, growth pattern or size of the plants are relevant in determining their use by H. erato phyllis.

Estrutura floral das angiospermas usadas por Heliconius erato phyllis (Lepidoptera, Nymphalidae) no Rio Grande do Sul, Brasil

A field survey of flowering plants used as food resource by the adults of Heliconius erato phyllis (Fabricius, 1775) was carried out in four sites located in Rio Grande do Sul state, Brazil. Samples were taken in preserved areas of the Atlantic Rain and Myrtaceae forests, an Eucalyptus plantation, and an urban park. Adult feeding frequencies on flowers were registered monthly from December 1996 to May 1997, on plants located on previously marked 200 m long transects. Flowers on which H. erato phyllis fed in the field were collected, drawn and morphometrically characterized. Feeding was registered on flowers of twenty-three species, of which seventeen are new records for H. erato in Brazil . The use of a given plant varied among localities, as a function of its corresponding abundance. The most visited flowers were those of Lantana camara L. and Stachytarpheta cayennensis (Rich.) Vahl, followed by Dahliapinnata Voss in the urban site. The data suggest the existence of size and shape convergence between the proboscis and the small, tubular flowers upon which H. eratophyllis feeds. They also indicate that H. eratophyllis adults have an opportunistic nectar feeding / pollen gathering habit, using several of those flowers available in a given time and locality that fit such a morphometrical pattern. Since plant species of both primitive and derived families are used, there is no indication that phylogenetic constraints play a major role in this association, nor that color of flowers, growth pattern or size of the plants are relevant in determining their use by H. erato phyllis.