Inventário da araneofauna (Arachnida, Araneae) de serapilheria na Estação Científica Ferreira Penna, Pará, Brasil

A Estação Científica Ferreira Penna (ECFP), com aproximadamente 33.000 hectares, está localizada na Floresta Nacional de Caxiuanã, Pará. Com o objetivo de implementar um protocolo estruturado de inventario da fauna de aranhas de serapilheira da ECFP, foi obtido um total de 400 amostras concentradas de 1m² de serapilheira, nos períodos chuvoso e seco. As aranhas foram segregadas através da combinação das técnicas de triagem manual e de extratores de Winkler. Estas amostras foram provenientes de cinco parcelas. Três parcelas estão localizadas em mata de terra firme (LBA-EXP, LBA-CON e TF-IMC) e duas em mata de igapó (1G-N e IG-S). Uma das parcelas de terra firme sofre estresse hídrico (LBA-EXP), sendo a chuva excluída do solo por meio de painéis e calhas. Foram coletados 2230 indivíduos (5,6 indivíduos / m², em média), pertencentes a 34 famílias. Sete famílias foram representadas apenas por animais imaturos: Nesticidae, Pisauridae, Gnaphosidae, Mimetidae, Deinopidae, Oxiopidae, Uloboridae. As famílias mais abundantes foram Salticidae, Theridiidae, Ctenidae, Oonopidae e Linyphiidae. Foi obtido um total de 876 indivíduos adultos, atribuídos a 120 espécies ou morfo-espécies, em 27 famílias. As espécies com maior abundância relativa foram Styposis sp.3 (Theridiidae) com 16,55% do total de indivíduos adultos, Pseudanapis sp.1 (Anapidae) com 6,96%, Meioneta sp.1 (Linyphiidae) com 6,39%, Oonopidae sp.1 com 5,59% e Salticidae sp.1 com 4,56%. Para a maioria das análises, foram excluídas 15 espécies consideradas como ocasionais na serapilheira. As curvas de acumulação de espécies observadas para o total de amostras e para cada uma das parcelas não atingiram assíntotas ao final da adição de amostras. Os padrões de abundância e incidência destas espécies indicam a existência de uma riqueza real de 123 a 184 espécies. As maiores estimativas de riqueza em espécies foram encontradas na parcela LBA-EXP (75 - 110 espécies). As menores estimativas foram observadas em IG-N (25 - 59 espécies). Apesar da riqueza em espécies e a abundância de aranhas ter sido maior na parcela LBA-EXP, a diversidade foi maior nas parcelas LBA-CON e TF-IMC. A diversidade no igapó foi mais baixa do que na terra firme. A composição de espécies diferiu entre os ambientes de terra firme e igapó, de acordo com coeficientes de similaridade e complementaridade percentual. A abundância e a riqueza de espécies de aranhas de serapilheira aumentam no período seco e diminuem com o aumento da umidade residual do solo.

Inventário da araneofauna (Arachnida, Araneae) do Parque Nacional de Sete Cidades, Piauí, Brasil

Foi realizado o inventário da araneofauna do Parque Nacional de Sete Cidades (municípios de Brasileira e Piracuruca, Piauí), utilizando amostragem padronizada para permitir comparações entre as assembléias de aranhas de seis fitofisionomias existentes na área de estudo e obter estimativas de riqueza. Utilizaram-se dados oriundos amostragem com armadilhas de queda (PTF), extratores de Winkler (WIN), guarda-chuva entomológico (GCE), rede de varredura (RV) e coletas manuais noturnas (MN), totalizando 1386 amostras; além do exame de todos os demais espécimes já coletados na área de estudo (n=1166). As análises estatísticas foram realizadas utilizando-se os dados obtidos com GCE, RV e MN. Ao todo, foram coletados 14.890 indivíduos (4491 adultos), segregados em 364 espécies. Destas, 72 foram determinadas a nível específico, 62 são novos registros para a área de estudo, 2 são novos registros para o Brasil e 48 foram reconhecidas como espécies novas por especialistas. A aplicação dos métodos GCE, RV e MN resultou em 11.085 aranhas, pertencentes a 303 espécies. As estimativas de riqueza variaram entre 355 (Bootstrap) e 467 (Jack 2). Entretanto o estimador que apresentou maior tendência a atingir a assíntota foi Chao 2 (403 spp.). A riqueza observada foi maior na mata seca semi-decídua (131 spp.), seguida pela mata de galeria (104 spp.), campo limpo (102 spp.), cerradão (91 spp.), cerrado típico (88 spp.) e cerrado rupestre (78 spp.). A eficiência dos métodos de coleta exibiu variação de acordo com a fitofisionomia onde o método foi aplicado, destacando-se a elevada eficiência da rede de varredura em áreas abertas. A composição de espécies variou entre as fitofisionomias e pode ser, em parte, explicada pela complexidade estrutural das áreas em questão. Os resultados das análises de agrupamento sugerem que em condições de dominância elevada, estes testes sejam realizados com coeficientes que utilizem dados qualitativos, a fim de anular-se o efeito da escolha do coeficiente e/ou a necessidade de transformação dos dados. De maneira geral, a araneofauna do Parque Nacional de Sete Cidades não segue padrões de agrupamento como sugerido para as análises botânicas, em que fitofisionomias campestre, savânicas e florestais são agrupadas.

A rare finding of mites (Arachnida: Acari: Leeuwenhoekiidae) parasitising a whip spider (Arachnida: Amblypygi: Charinidae)

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

Community structure of mites (Arachnida: Acari) in six rubber tree clones

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

From cuckoos to chickens: a caught-in-the-act case of host shift in feather mites (Arachnida: Acari: Psoroptoididae)

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

Amostragem diurna versus noturna de ácaros (Arachnida: Acari) associados a Genipa americana L. (Rubiaceae)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Influência de Cecropia pachystachya na incidência de ácaros (Arachnida, Acari) e de Leptopharsa heveae (Insecta, Hemiptera) em cultivo de seringueira

Cecropia pachystachya is a plant native to the states of Mato Grosso and São Paulo, usually found in rubber tree plantations. The goals of this study were to verify: a) whether the presence of C. pachystachya in rubber tree plantations influences the occurrence of mites in rubber trees; b) whether it can be used as a reservoir of predaceous mites; c) whether it serves as an alternative host for Leptopharsa heveae during the natural senescence of rubber trees. This study was conducted in two rubber tree plantations in São José do Rio Preto, in the state of São Paulo, Brazil. One of them had numerous naturally growing individuals of C. pachystachya, while the other was free of spontaneous plants. We registered high richness of predaceous mites on C. pachystachya, but only 37.5% of them were found on rubber trees, which reveals low displacement rate of mites between the plants. Among the species that were common to both plants, only the predaceous Zetzellia agistzellia and the phytophagous mites Allonychus brasiliensis and Eutetranychus banksi were influenced by the presence of C. pachystachya. The incidence of L. heveae did not differ between the plantations under study and, moreover, C. pachystachya was not used as an alternative host by this insect, since no individuals were registered on its leaves during the natural senescence of rubber trees.

New systematic assignments in Gonyleptoidea (Arachnida, Opiliones, Laniatores)

As part of an ongoing revision of the family Gonyleptidac, we have identified many species that are synonyms of previously described species or misplaced in this family. This article summarizes these findings, adding previously unavailable information or correcting imprecise observations to justify the presented taxonomic changes. The following new familial or subfamilial assignments are proposed: Nemastygnus Roewer, 1929 and Taulisa Roewer, 1956 are transferred to Agoristenidae, Agoristeninae; Napostygnus Roewer, 1929 to Cranaidae; Ceropachylinus peruvianus Roewer, 1956 and Pirunipygus Roewer, 1936 are transferred to Gonyleptidae, Ampycinae; Gyndesops Roewer, 1943, Haversia Roewer, 1913 and Oxapampeus Roewer, 1963 are transferred to Gonyleptidae, Pachylinae. The following generic synonymies are proposed for the family Gonyleptidae: Acanthogonyleptes Mello-Leitao, 1922 = Centroleptes Roewer, 1943; Acrographinotus Roewer, 1929 = Unduavius Roewer, 1929; Gonyleptes Kirby, 1819 = Collonychium Bertkau, 1880; Mischonyx Bertkau, 1880 = Eugonyleptes Roewer, 1913 and Gonazula Roewer, 1930; Parampheres Roewer, 1913 = Metapachyloides Roewer, 1917; Pseudopucrolia Roewer, 19 12 = Meteusarcus Roewer, 1913; Haversia Roewer, 19 13 = Hoggellula Roewer, 1930. The following specific synonymies are proposed for the family Gonyleptidae: Acanthogonyleptes singularis (Mello-Leitao, 1935) = Centroleptes flavus Roewer, 1943, syn. n.; Geraeocormobius sylvarum Holmberg, 1887 = Discocyrtus serrifemur Roewer, 1943, syn. n.; Gonyleptellus bimaculatus (Sorensen, 1884) = Gonyleptes cancellatus Roewer, 1917, syn. n.; Gonyleptes atrus Mello-Leitao, 1923 = Weyhia brieni Giltay, 1928, syn. n.; Gonyleptes fragilis Mello-Leitao, 1923 = Gonyleptes banana Kury, 2003, syn. n.; Gonyleptes horridus Kirby, 1819 = Collonychium bicuspidatum Bertkau, 1880, syn. n., Gonyleptes borgmeyeri Mello-Leitao, 1932, syn. n., Gonyleptes curvicornis Mello-Leitao, 1932, syn. n., Metagonyleptes hamatus Roewer, 1913, syn. n. and Paragonyleptes simoni Roewer, 1930, syn. n.; Gonyleptes pustulatus Sorensen, 1884 = Gonyleptes guttatus Roewer, 1917, syn. n.; Haversia defensa (Butler, 1876) = Sadocus vallentini Hogg, 1913, syn. n.; Liogonyleptoides minensis (Piza, 1946) = Currala bahiensis Soares, 1972, syn. n.; Megapachylus grandis Roewer, 1913 = Metapachyloides almeidai Soares & Soares, 1946, syn. n.; Mischonyx cuspidatus (Roewer, 1913) = Gonazula gibbosa Roewer, 1930 syn. n.; Mischonyx scaber (Kirby, 1819) = Xundarava holacantha Mello-Leitao, 1927, syn. n.; Parampheres tibialis Roewer, 1917 = Metapachyloides rugosus Roewer, 1917, syn. n.; Parapachyloides uncinatus (Sorensen, 1879) = Goyazella armata Mello-Leitao, 1931, syn. n.; Pseudopucrolia mutica (Perry, 1833) = Meteusarcus armatus Roewer, 1913, syn. n. The following new combinations are proposed: Acrographinotus ornatus (Roewer, 1929), comb. n. (ex Unduavius); Gonyleptellus bimaculatus (Sorensen, 1884), comb. n. (ex Gonyleptes); Gonyleptes perlatus (Mello-Leitao, 1935), comb. n. (ex Moojenia); Mischonyx scaber (Kirby, 1819), comb. n. (ex Gonyleptes); and Neopachyloides peruvianus (Roewer, 1956), comb. n. (ex Ceropachylus). The following species of Gonyleptidae, Gonyleptinae are revalidated: Gonyleptes atrus Mello-Leitao, 1923 and Gonyleptes curvicornis (Roewer, 1913).

Descriptions of Thereza murutinga sp. nov. and Pristocnemis caipira sp. nov., and new records of Caelopyginae (Opiliones: Laniatores: Gonyleptidae)

Two new species of Caelopyginae are described: Pristocnemis caipira sp. nov. from Parque Nacional da Serra da Canastra, Minas Gerais, Brazil, and Thereza murutinga sp. nov., from Parati, Rio de Janeiro, Brazil. Pristocnemis caipira sp. nov. is diagnosed by shallow grooves on the dorsal scutum, a lower number of tarsal segments, presence of a spine on the anal operculum, large, pointed tubercles on the lateral margins of the dorsal scutum, and an absence of white patches on the dorsal scutum. Thereza murutinga sp. nov. is diagnosed by the combination of the following characters: incomplete median longitudinal groove on area III and absent on area II, prosoma much smaller than opisthosoma, and a large white patch covering the prosoma and whole areas of the opisthosomal scutum. A cladistic analysis including the two new species was performed to investigate their relationship within the subfamily. We obtained 927 trees of 185 steps (CI=0.4, RI=0.74), which corroborated the generic assignments of the new species, but infrageneric relationships remained unsolved. In addition, male genitalia of Ampheres luteus (Giltay) and genera Pristocnemis and Thereza are redescribed, new distribution records for Caelopyginae species are presented, and biogeographical implications are discussed.

Behavioral analysis of the interaction between the spitting spider Scytodes globula (Araneae: Scytodidae) and the harvestman Discocyrtus invalidus (Opiliones: Gonyleptidae)

Spitting spiders (Scytodidae) have a distinct predatory strategy in which they eject a sticky secretion from their cheliceral fangs to immobilize prey. This behavior could potentially allow the spider not only to avoid defensive secretions but also to bite specific vulnerable spots of a potential prey such as a harvestman. We used an ethogram, a fluxogram and an experiment to analyze the interaction between the harvestman Discocyrtus invalidus Piza 1938 (Arachnida: Opiliones) and the syntopic spider Scytodes globula (Nicolet 1849) (Arachnida: Araneae). These spiders, while readily taking crickets as prey, seldom spat at and never bit the harvestmen, which apparently did not exude repugnatorial secretions. We therefore tested, by clogging the glands and using appropriate controls, whether non-visible amounts of secretions could cause the rejection, but the harvestmen were still refused. This is the first detailed and quantified description of an interaction between a spitting spider and a harvestman. The general conclusions are that S. globula avoids preying on D. invalidus, S. globula behaves differently when attacking harvestmen and crickets and the scent gland secretions of D. invalidus do not play a direct role in this predator-prey interaction.

A new species of Cryptocellus (Arachnida: Ricinulei) from Eastern Amazonia

Cryptocellus canga sp. nov. is described from specimens collected in several caves at Carajás National Forest, Pará, Brazil. The new species differs from other species of the genus by the morphology of copulatory apparatus of the male leg III.

Silhouettella loricatula (Arachnida, Araneae, Oonopidae): a Haplogyne spider with complex female genitalia

The female genital system of the oonopid Silhouettella loricatula is astonishingly complex. The genital opening is situated medially and leads into an oval receptaculum that is heavily sclerotized except for the ventral half of the posterior wall that appears chitinized only. A large striking sclerite lying in the posterior wall of the uterus externus is attached anteriorly to the receptaculum and continues dorsally into a globular appendix that bears a furrow. The uterus externus shows a peculiar modification in its anterior wall: a paddle-like sclerite with a nail-like posterior process. This sclerite lies opposite to the furrow proceeding in the globular appendix and may serve females to lock the uterus externus by muscle contractions. Massive muscles connect the sclerite with the anterior scutum of the opisthosoma and with two other sclerites that are attached to the receptaculum and serve as attachments for further muscles. Gland cells extend around a pore field of the receptaculum. They produce secretion that encloses spermatozoa in a discrete package (secretory sac) inside the receptaculum. In this way, the mixing of sperm from different males and thus sperm competition may be severely limited or completely prevented. During a copulation in the laboratory the ejection of a secretory sac that most probably contained spermatozoa was observed, indicating sperm dumping in S. loricatula. The ejection of the secretory sac may be caused by female muscle contractions or by male pedipalp movements. The majority of the investigated females have microorganisms in the receptacula that could represent symbionts or infectious agents. The microorganisms can be identified partly as bacteria. They are enclosed in secretion and are always found in the same position inside the receptaculum.

Complex genital system of a haplogyne spider (Arachnida, Araneae, Tetrablemmidae) indicates internal fertilization and full female control over transferred sperm

The female genital organs of the tetrablemmid Indicoblemma lannaianum are astonishingly complex. The copulatory orifice lies anterior to the opening of the uterus externus and leads into a narrow insertion duct that ends in a genital cavity. The genital cavity continues laterally in paired tube-like copulatory ducts, which lead into paired, large, sac-like receptacula. Each receptaculum has a sclerotized pore plate with associated gland cells. Paired small fertilization ducts originate in the receptacula and take their curved course inside the copulatory ducts. The fertilization ducts end in slit-like openings in the sclerotized posterior walls of the copulatory ducts. Huge masses of secretions forming large balls are detectable in the female receptacula. An important function of these secretory balls seems to be the encapsulation of spermatozoa in discrete packages in order to avoid the mixing of sperm from different males. In this way, sperm competition may be completely prevented or at least severely limited. Females seem to have full control over transferred sperm and be able to express preference for spermatozoa of certain males. The lumen of the sperm containing secretory balls is connected with the fertilization duct. Activated spermatozoa are only found in the uterus internus of females, which is an indication of internal fertilization. The sperm cells in the uterus internus are characterized by an extensive cytoplasm and an elongated, cone-shaped nucleus. The male genital system of I. lannaianum consists of thick testes and thin convoluted vasa deferentia that open into the wide ductus ejaculatorius. The voluminous globular palpal bulb is filled with seminal fluid consisting of a globular secretion in which only a few spermatozoa are embedded. The spermatozoa are encapsulated by a sheath produced in the genital system. The secretions in females may at least partly consist of male secretions that could be involved in the building of the secretory balls or play a role in sperm activation. The male secretions could also afford nutriments to the spermatozoa.