Occurrence, distribution and abundance of Halobates micans Eschscholtz, 1822 (Heteroptera, Gerridae) along the southeastern Brazilian coast

Data collected during an oceanographic cruise along the southeastern Brazilian coast from Cape Frio (22° 58' S) and Paraná (27° 50' S) in March 1982 showed that the marine insect Halobates micans occurred along the Southeastern Brazilian Bight, but in lower abundance in low-temperature areas due to the intrusion and upwelling of South Atlantic Central Water, and in low-salinity areas in Coastal Water. Insect capture was higher at night and in the oligotrophic Tropical Water. The number of nymphs and adult females was higher, probably because of an active breeding season during the austral summer. Adult sex ratio was 1.3:1.0 (F:M). Floating gas vesicles of benthic Sargassum spp. and petroleum lumps were used by females for egg-laying.

A SUBFAMÍLIA GERRINAE (HEMIPTERA: HETEROPTERA: GERRIDAE) NA BACIA HIDROGRÁFICA DO RIO TROMBETAS, PARÁ, BRASIL

Foi realizado um levantamento da Família Gerridae na Bacia Hidrográfica do rio Trombetas, Pará, Brasil, desde as cabeceiras até o Baixo Trombetas. Entre os Hemiptera aquático, Gerridae foi a Família mais representativa, sendo Gerrinae a subfamília mais coletada em 12 dos 35 pontos de coleta. Mapas com os primeiros registros da distribuição geográfica de Gerrinae para a Bacia do rio Trombetas e uma chave para a identificação dos cinco gêneros e seis espécies são apresentadas.

Efeito de fatores abióticos sobre Brachymetra albinervis albinervis (Heteroptera: Gerridae)

RESUMO Analisou-se a influência de fatores abióticos, distribuição longitudinal e temporal sobre a abundância de Brachymetra albinervis albinervis Amyot & Serville, 1843. Foram avaliados três sítios de um riacho de Cerrado: nascente, intermediário e foz, mensalmente durante um ano (junho de 2011 a maio de 2012). As variáveis abióticas aferidas foram: oxigênio dissolvido, temperatura da água, pH, condutividade elétrica, largura e profundidade do riacho. Em cada sítio, mensalmente coletou-se em transecção de 100 m lineares. Foram coletados 111 espécimes. A foz apresentou menor abundância quando comparada aos outros locais (F(2, 9) 13,721, p = 0,001). A abundância não variou entre os períodos do ano (chuva, vazante, seca ou início da chuva). Assim, a alteração na abundância de B. a. albinervisanalisada ao longo de um ano foi influenciada pelos trechos do córrego, e essa variação foi atribuída a alterações ambientais no sítio foz que apresentou menor abundância e consequentemente é o que apresenta menor integridade ambiental. Esses resultados contribuem para o conhecimento ecológico dessa espécie e discute sobre a mudança da ocorrência da espécie em função da alteração dos ambientes aquáticos.

Alguns aspectos morfológicos de Brachymetra albinervus (Amyot & Serville, 1843) (Hemiptera - Gerridae)

Descrevemos neste trabalho a morfologia externa de uma forma áptera de Brachymetra albinervus (Amyot & Serville, 1843), dando especial atenção ao estudo da genitália. Fornecemos ainda uma crítica aos trabalhos existentes sobre esta espécie e uma pequena discussão sobre as características atípicas nela encontradas.

Estudo morfológico de Limnogonus aduncus Drake & Harris, 1932 e Halobatopsis platensis (Berg, 1879) e suas genitálias externas (Hemiptera - Gerridae)

Com o intuito de elucidar a cosntituição da genitália masculina e criar novos parâmetros para serem usados em taxionomia, estudamos Limnogonus aduncus Drake & Harris, 1932 - Gerrinae e Halobatopsis platensis (Berg, 1879) - Trepobatinae, evidenciamenos 11 estruturas no falo e comprovamos uma nítida separação entre estas duas subfamílias, não só pela disposição como também pela forma do aparelho articular, vesica, falosoma, suporte do falosoma, conjuntiva e parâmetros.

Heteropicnotic chromatin and nucleolar activity in meiosis and spermiogenesis of Limnogonus aduncus (Heteroptera, Gerridae): a stained nucleolar organizing region that can serve as a model for studying chromosome behavior.

Males of Limnogonus aduncus were found to have the sex chromosome system X0 and chromosome number 2n = 23 (22A + X0). Testis cells were stained with lacto-acetic orcein and silver nitrate so that changes in the morphology and degree of staining of the heteropicnotic chromatin and the nucleolar material could be observed during meiosis and spermiogenesis. These structures share the same nuclear position and could be seen until almost the end of spermiogenesis. A chromosome region stained with silver nitrate was indicative of a nucleolar organizing region (NOR), which is rarely detected in Heteroptera with this technique. The NOR is located at one end of a single member of an autosome pair. The finding of this stained region enabled us to observe that the telomeric association of sister chromatids that characterizes the Heteroptera does not include the chromosome ends, where NORs are located; we also observed in anaphase that the chromosome end through which it is pulled to the pole is the one containing the NOR. Another observation was that the single nucleolar body present in the cells at anaphase never goes to the cell pole that does not receive the NOR. We conclude that L. aduncus is a good model for cytogenetic studies involving nucleolar activity and also may be useful for studying the mechanisms of activation and inactivation of kinetic activity at the chromosome ends. Although the chromosomes of Heteroptera are known to be holocentric, whether kinetic activity is restricted to one or involves both chromosome ends is still not well understood.

Spermatogenesis and karyotypes of three species of water striders (Gerridae, Heteroptera).

Although they are of economic importance, there have been few cytogenetic studies of the Gerridae (Heteroptera) in Brazil. We examined spermatogenesis (meiosis and spermiogenesis) and nucleolar behavior in three species of the family Gerridae. Brachymetra albinerva and Halobatopsis platensis were found to have a chromosome complement of 2n = 25 (24A + X0) and Cylindrostethus palmaris 2n = 29 (28A + X0) chromosomes. Fifteen individuals of these species were collected from the reservoir of São José do Rio Preto, SP, using screens and were transported in pots containing water to the laboratory, where cytogenetic preparations were made. The polyploidy nuclei are formed by several heteropyknotic regions; cells in meiotic prophase have a heteropyknotic region that is probably the sex chromosome, and the chromosomes from chiasmata. The spermatids are rounded and have a heteropyknotic region at the periphery of the nucleus; the sperm head is small, with a long tail. Silver impregnation of meiotic cells showed one or more disorganized bodies around the perichromosomal sheath. The round spermatids had two bodies next to each other, but these were elongated; one of the bodies remained in the head and the other migrated to the initial part of the tail at the end of spermagenesis, when the staining was no longer evident. The meiotic cells appear during spermatogenesis and have very similar silver-impregnation patterns in different species of Heteroptera.

Relacionamento filogenético entre espécies pertencentes às famílias Belostomatidae, Gelastocoridae, Gerridae, Notonectidae, Veliidae (Hemiptera: Heteroptera) e Cercopidae (Hemiptera:Auchenorrhyncha)

Pós-graduação em Genética - IBILCE

Cytogenetics Analysis and Testis Morphology of Aquatic Species of the Families Belostomatidae, Gelastocoridae, Gerridae, Notonectidae, and Veliidae (Heteroptera)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Keys to subfamilies, tribes, genera and subgenera of the Gerridae of the world

University of Kansas, Department of Entomology contribution no. 1047.

Spermatogenesis and nucleolar behavior in males of aquatic Heteroptera

Aspects of spermatogenesis and nucleolar behavior were analyzed in Brachymetra albinerva, Cylindrostethus palmaris, Halobatopsis platensis, Limnogonus aduncus (Gerridae), Martarega sp (Notonectidae), Rhagovelia whitei, and Rhagovelia sp (Veliidae). The testicles are rounded (Veliidae), elongated (Gerridae) or spiral (Notonectidae) and have a transparent membrane covering them. The complement chromosome was 2n = 23 (22A + X0, L. aduncus and Rhagovelia sp), 25 (24A + X0, B. albinerva and H. platensis), 26 (22A + 2m + XY, Martarega sp), 29 (28A + X0, C. palmaris), or 39 (38A + X0, R. whitei) chromosomes, and the only species with a different sex chromosome system was Martarega sp, which showed an XY system and m-chromosomes. The meiotic behavior of all species was similar: holocentric chromosomes and heteropyknotic material at prophase, interstitial and/or terminal chiasmata, and first reductional division for the autosomes and the reverse for the sex chromosomes. The only difference observed was related to the very large size of Martarega sp cells in all stages of spermatogenesis. With regard to nucleolar behavior, the species did not show differences, except for Martarega sp with larger nucleoli than the other species. The only species in which it was clearly possible to identify the nucleolar organizer region was L. aduncus, in the region of a terminal autosome. It was also confirmed that the telomeric associations do not occur at random. In the other species, specific staining was very discrete, and the nucleolar organizer region location was not at all evident.

Spermatogenesis of riffle bugs, Rhagovelia whitei and Rhagovelia sp (Veliidae), and backswimmers Martarega sp (Notonectidae).

We examined the course of spermatogenesis and the meiotic chromosome complements in aquatic species of true bugs, Heteroptera. The chromosome complement of the Veliidae species was 2n = 39 (38A + X0) and 23 (22A + X0) in Rhagovelia whitei and Rhagovelia sp, respectively, and in the species of the Notonectidae (Martarega sp) it was 26 (22A + 2m + XY); all collected from the region of São José do Rio Preto, SP, Brazil. An impressive characteristic of the first analysis was the size of the cells belonging to Martarega sp, which were six times larger than the same cells in Pentatomidae and twice as large as the cells in aquatic Heteroptera (Gerridae). Regarding spermatogenesis, all the species analyzed showed the same pattern: holocentric chromosomes and elongated spermatids with the chromatin distributed evenly along the head. The family Veliidae showed several bodies impregnated with silver nitrate at prophase, while the family Notonectidae displayed only one. The cells of Notonectidae also showed an evident and round body until the end of prophase I and in the family Veliidae the silver-impregnated bodies were disorganized, where the only region visualized was possibly that of the NOR. In metaphase, silver-stained regions were found at the periphery of all chromosomes in Veliidae and at the periphery of some chromosomes in Notonectidae. The spermatids of Veliidae showed a less silver-impregnated vesicle, while Notonectidae showed silver staining only in part of the nuclear membrane. Therefore, families of Heteroptera have some differences and features that can help identify and classify these species.

Espermatogênese e comportamento nucleolar em machos de Heteoptera aquáticos

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Spermatogenesis of riffle bugs, Rhagovelia whitei and Rhagovelia sp (Veliidae), and backswimmers Martarega sp (Notonectidae)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

New records and distribution expansion for Neotropical water-striders (Insecta: Heteroptera: Gerromorpha)

Based on material from several collections, summarized distributions and new records are presented for selected Neotropical species of Gerromorpha of the families Gerridae (Brachymetra albinervis albinervis, B. furva, B. lata, B. shawi, Cylindrostethus erythropus, C. linearis, C. palmaris, C. regulus, Halobatopsis platensis, Limnogonus aduncus aduncus, L. hyalinus, L. ignotus, L. profugus, L. recurvus, Neogerris lubricus, N. magnus, N. lotus, N. visendus, Ovatametra gualeguay, Rheumatobates crassifemur crassifemur, R. c. esakii, Tachygerris adamsoni, T. celocis and T. surinamensis), Hydrometridae (Hydrometra guianana and H. sztolcmani) and Mesoveliidae (Mesovelia amoena, M. mulsanti and Mesoveloidea williamsi).