Oligochaetes (Annelida, Clitellata) in a neotropical stream: a mesohabitat approach

This paper analyses the relationship among mesohabitat and aquatic oligochaete species in the Galharada Stream (Campos do Jordão State Park, state of São Paulo, Brazil). Between August 2005 and May 2006 a total of 192 samples were obtained in areas of four different mesohabitats: riffle leaf litter (RL), pool leaf litter (PL), pool sediment (PS) and interstitial sediment from rocky beds in riffle areas (IS). In the mesohabitats sampled, 2007 specimens were identified, belonging to two families (Naididae and Enchytraeidae). Among the oligochaetes identified Naididae was represented by six genera (Allonais, Chaetogaster, Nais, Pristina, Aulodrilus and Limnodrilus). Principal components analysis (PCA) revealed the first two axes explained 85.1% of the total variance of the data. Limnodrilus hoffmeisteri Claparede, 1862 and Aulodrilus limnobius Bretscher, 1899 were associated with the pool areas (PL and PS). Most species of genera Pristina and Nais demonstrated apparent affinity with the riffle mesohabitats. The Indicator Species Analysis (IndVal) revealed that Nais communis Piguet, 1906, Pristina leidyi Smith, 1896 and Pristina (Pristinella) jenkinae (Stephenson, 1931) are indicative of RL mesohabitat, while family Enchytraeidae was considered indicative of PL mesohabitat.

Synchaeta jollyae (Shiel & Koste) (Rotifera, Synchaetidae): an overlooked species or a newcomer in Neotropical freshwaters?

Populations of Synchaeta jollyae (Shiel & Koste, 1993) (Rotifera), a species recently recorded for the first time in Brazil and South America, were analyzed in reservoirs in Southeast Brazil. Sampling was carried out monthly from August 2006 to July 2007 at Furnas Reservoir in the Rio Grande basin, state of Minas Gerais, and in four cascade reservoirs in the Tietê River basin (Barra Bonita, Bariri, Ibitinga and Nova Avanhandava) state of São Paulo, in June and September 2008 and in January and May 2009. Synchaeta jollyae occurred in most samples and periods. From the results obtained it is evident that S. jollyae occurs in water bodies of varied trophic status but reaches larger populations in eutrophic water bodies and during lower temperature periods. The greatest densities of S. jollyae were found in the eutrophic Bariri Reservoir, on the Tietê River, during the winter. Mann-Whitney test confirmed the significant difference between the population densities in periods of high and low temperatures, with populations reaching higher densities at lower temperatures. It is not yet possible to tell whether S. jollyae is a widely distributed species that has been overlooked in previous plankton studies in South America. Wherever these populations of S. jollyae might have originated, it appears to be a species well established and adapted to a wide range of conditions in the Neotropics.

Population ecology of the multivoltine Neotropical gall midge Eugeniamyia dispar (Diptera, Cecidomyiidae)

Our understanding of the population ecology of insect gallers is largely built on examples from temperate zones, but tropical and subtropical gallers may present distinct patterns of abundance and distribution across time. Eugeniamyia dispar Maia, Mendonça & Romanowski, 1996 is a multivoltine Neotropical cecidomyiid that induces spongy leaf galls on Eugenia uniflora (Myrtaceae). Galls were censused in the urban area of Porto Alegre, southern Brazil on six plants at two sites, for two years, at roughly weekly intervals. Overall 9,694 eggs, galling attempts and galls were counted. New galls continuously appear on developing leaves, but galls with live inducers are absent from June to at least early August. Galls on a same shoot develop synchronically, thus the shoot is probably the unit for oviposition. Given the also synchronic appearance of galls on different plants on a site, it seems midges can disperse and attack close-by plants. Gall cohorts varied in abundance by two orders of magnitude; there were more galls during summer than for spring and autumn, in a wave-like pattern. Host plant leaf production was seasonal, with low production during winter and cyclic production during the rest of the year. Perhaps because of this very variable pattern, gall abundance did not follow leaf production: this galler is not synchronised with its host at least during most of the year. This multivoltine gall inducer with "labile" galls, short development time, partially overlapping generations and low host synchronisation differs from the commonly studied species of the temperate regions providing a subject for ecological comparisons.

Escarabeíneos copro-necrófagos (Coleoptera, Scarabaeidae, Scarabaeinae) de fragmentos de Mata Atlântica em Silveira Martins, Rio Grande do Sul, Brasil

A fauna de Scarabaeinae (Coleoptera: Scarabaeidae) foi amostrada através de armadilhas de queda iscadas com excremento humano e peixe apodrecido em fragmentos florestais de Silveira Martins, Rio Grande do Sul, Brasil, de novembro de 2010 a janeiro de 2011. Foi coletado um total de 1.611 indivíduos, pertencentes a seis tribos, 11 gêneros e 28 espécies. As espécies mais abundantes foram Canthon latipes Blanchard, 1845 (49,9%), C. chalybaeus Blanchard, 1845 (13,9%), Deltochilum sculpturatum Felsche, 1907 (4,9%) e Eurysternus caribaeus (Herbst, 1789) (4,3%), que juntas representaram 73% do total de indivíduos capturados. As armadilhas iscadas com excremento humano capturaram maior número de espécies do que as iscadas com peixe apodrecido. Não houve diferença estatística significativa entre os tipos de iscas utilizados em relação à abundância de Scarabaeinae. A maior parte da comunidade de Scarabaeinae capturada foi representada por espécies de hábito alimentar generalista e comportamento escavador. A comunidade amostrada segue os padrões gerais de estrutura trófica e comportamental de Scarabaeinae encontrados por toda a região Neotropical.

Meddelanden af Societas pro Fauna et Flora Fennica.

Haft. 27 (1900-1901)

Meddelanden af Societas pro Fauna et Flora Fennica.

Haft. 23 (1896-1897)

Meddelanden af Societas pro Fauna et Flora Fennica.

Haft. 25 (1898-1899)

Meddelanden af Societas pro Fauna et Flora Fennica.

Haft. 29 (1902-1903)

Meddelanden af Societas pro Fauna et Flora Fennica.

Haft. 37 (1910-1911)

Meddelanden af Societas pro Fauna et Flora Fennica.

Haft. 24 (1897-1898)

Meddelanden af Societas pro Fauna et Flora Fennica.

Haft. 26 (1899-1900)

Meddelanden af Societas pro Fauna et Flora Fennica.

Haft. 35 (1908-1909)

Meddelanden af Societas pro Fauna et Flora Fennica.

Haft. 34 (1907-1908)