11 resultados para Epigeous
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Epigeous termite mounds are frequently observed in pasture areas, but the processes regulating their population dynamics are poorly known. This study evaluated epigeous termite mounds in cultivated grasslands used as pastures, assessing their spatial distribution by means of geostatistics and evaluating their vitality. The study was conducted in the Cerrado biome in the municipality of Rio Brilhante, Mato Grosso do Sul, Brazil. In two pasture areas (Pasture 1 and Pasture 2), epigeous mounds (nests) were georeferenced and analyzed for height, circumference and vitality (inhabited or not). The area occupied by the mounds was calculated and termite specimens were collected for taxonomic identification. The spatial distribution pattern of the mounds was analyzed with geostatistical procedures. In both pasture areas, all epigeous mounds were built by the same species, Cornitermes cumulans. The mean number of mounds per hectare was 68 in Pasture 1 and 127 in Pasture 2, representing 0.4 and 1 % of the entire area, respectively. A large majority of the mounds were active (vitality), 91 % in Pasture 1 and 84 % in Pasture 2. A “pure nugget effect” was observed in the semivariograms of height and nest circumference in both pastures reflecting randomized spatial distribution and confirming that the distribution of termite mounds in pastures had a non-standard distribution.
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This work, dedicated to the study of nesting habits of the species of the Neotropical genus Partamona Schwarz, is a sequence to the taxonomic revision recently published elsewhere. A total of 214 nests and nest aggregations of 18 species [Partamona epiphytophila Pedro & Camargo, 2003; P. testacea (Klug, 1807); P. mourei Camargo, 1980; P. vicina Camargo, 1980; P. auripennis Pedro & Camargo, 2003; P. combinata Pedro & Camargo, 2003; P. chapadicola Pedro & Camargo, 2003; P. nhambiquara Pedro & Camargo, 2003; P. ferreirai Pedro & Camargo, 2003; P. pearsoni (Schwarz, 1938); P. gregaria Pedro & Camargo, 2003; P. batesi Pedro & Camargo, 2003; P. ailyae Camargo, 1980; P. cupira (Smith, 1863); P. mulata Moure in Camargo, 1980; P. seridoensis Pedro & Camargo, 2003; P. criptica Pedro & Camargo, 2003; P. helleri (Friese, 1900)] were studied , including data about habitat, substrate, structural characteristics, construction materials and behavior. The descriptions of the nests are illustrated with 48 drawings. Partial data of the nests of P. bilineata (Say, 1837), P. xanthogastra Pedro & Camargo, 1997, P. orizabaensis (Strand, 1919), P. peckolti (Friese, 1901), P. aequatoriana Camargo, 1980, P. musarum (Cockerell, 1917) and P. rustica Pedro & Camargo, 2003 are also presented. Nests of P. grandipennis (Schwarz, 1951), P. yungarum Pedro & Camargo, 2003, P. subtilis Pedro & Camargo, 2003, P. vitae Pedro & Camargo, 2003, P. nigrior (Cockerell, 1925), P. sooretamae Pedro & Camargo, 2003 and P. littoralis Pedro & Camargo, 2003 are unknown. The species of Partamona build notable nest entrance structures, with special surfaces for incoming / exiting bees; some of them are extremely well-elaborated and ornamented, serving as flight orientation targets. All species endemic to western Ecuador to Mexico with known nesting habits (P. orizabaensis, P. peckolti, P. xanthogastra, P. bilineata, P. aequatoriana and P. musarum) build their nests in several substrates, non-associated with termitaria, such as cavities and crevices in walls, among roots of epiphytes and in bases of palm leaves, in abandoned bird nests, under bridges, and in other protected places, except P. peckolti that occasionally occupies termite nests. In South America, on the eastern side of the Andes, only P. epiphytophila and P. helleri nest among roots of epiphytes and other substrates, non-associated with termitaria. All other species studied (P. batesi, P. gregaria, P. pearsoni, P. ferreirai, P. chapadicola, P. nhambiquara, P. vicina, P. mourei, P. auripennis, P. combinata, P. cupira, P. mulata, P. ailyae, P. seridoensis, P. criptica and P. rustica) nest inside active termite nests, whether epigeous or arboreous. The only species that builds obligate subterranean nests, associated or not with termite or ant nests (Atta spp.) is P. testacea. Nests of Partamona have one vestibular chamber (autapomorphic for the genus) closely adjacent to the entrance, filled with a labyrinth of anastomosing pillars and connectives, made of earth and resins. One principal chamber exists for food and brood, but in some species one or more additional chambers are filled with food storage pots. In nests of P. vicina, there is one atrium or "false nest", between the vestibule and the brood chamber, which contains involucral sheaths, cells and empty pots. All structures of the nest are supported by permanent pillars made of earth and resins (another autapomorphy of the genus). The characters concerning nesting habits were coded and combined with morphological and biogeographic data, in order to hypothesize the evolutive scenario of the genus using cladistic methodology. The phylogenetic hypothesis presented is the following: (((((P. bilineata (P. grandipennis, P. xanthogastra)) (P. orizabaensis, P. peckolti)) (P. aequatoriana, P. musarum)) P. epiphytophila, P. yungarum, P. subtilis, P. vitae) (((((P. testacea (P. mourei, P. vicina)) (P. nigrior (P. auripennis, P. combinata))) (P. ferreirai (P. pearsoni (P. gregaria (P. batesi (P. chapadicola, P. nhambiquara)))))) ((((P. ailyae, P. sooretamae) P. cupira, P. mulata) P. seridoensis) P. criptica, P. rustica, P. littoralis)) P. helleri))). One area cladogram is presented. Dates of some vicariance / cladogenesis events are suggested. For bilineata / epiphytophila group, which inhabits the Southwestern Amazonia and the Chocó-Mexican biogeographical components, the origin of ancestral species is attributed to the Middle Miocene, when the transgressions of the Maracaibo and Paranense seas isolated the tropical northwestern South America from the eastern continental land mass. The next cladogenic event in the history of the bilineata / epiphytophila group is attributed to the Plio-Pleistocene, when the Ecuadorian Andes reached more than 3000 m, and the ancestral species was fragmented in two populations, one occupying the western Andes (ancestral species of the bilineata subgroup) and other the southwestern Amazon (ancestral species of the epiphytophila subgroup). Other aspects of the history of Partamona are also discussed.
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Epigean ant communities in Atlantic Forest remnants of São Paulo: a comparative study using the guild concept. The guilds constitute a valuable ecological tool, because they allow conducting comparisons among environments under different conditions. The ants can be used as ecological indicators, mainly for the monitoring of degraded forest areas. The aim of this research was to study guild organization among the epigeous Formicidae living in Atlantic forest remnants of the State of São Paulo, Brazil. Ant collections were performed in three distinct Atlantic forest biome areas: arboreal littoral vegetation ("restinga") (Cananéia), semideciduous seasonal forest (Piracicaba) and dense ombrophylousforest (Pariquera-Açu). After identification, the ants were grouped into guilds, based on the ecological attributes of behavior and habit, according to the literature. Nine guilds were found; the semideciduous seasonal forest ecosystem presented eight of them, followed by the arboreal sandbank (7) and dense ombrophylous forest (6). The guilds found were: litter omnivorous and scavengers, granivorous species, specialist predators living in litter and soil, litter generalist predators, subterranean mealybug-dependent species, army ants, dominant or subdominants arboreal, that occasionally forage on the ground, soil or litter dominant and fungus-growers, using feces and insect body fragments. The guilds found can be used in the monitoring of the mirmecofauna in the Atlantic Forest biome, supplying insights for further ecological studies.
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Plântulas de Cybistax antisyphilitica (ipê-verde), espécie arbórea que ocorre no Estado de São Paulo, Brasil, foram estudadas morfoanatomicamente e citogeneticamente. As plântulas são eudicotiledôneas, fanerocotiledonares e epigéias. Suas sementes apresentam alas hialinas, assimétricas e de textura papirácea. A raiz é axial com tecido epidérmico irregular. O hipocótilo é verde, glabro e apresenta os elementos do xilema em diferenciação. Os cotilédones são verdes, foliáceos, reniformes, com mesofilo heterogêneo, epiderme pilosa e feixes vasculares colaterais. Os eófilos são glabros, peciolados, de filotaxia oposta, dorsiventrais, hipoestomáticos e possuem mesofilo heterogêneo e assimétrico. Não há diferenças anatômicas significativas entre os eófilos e os metáfilos. O sistema vascular do pecíolo dos metáfilos dispõe-se em forma de ferradura. A espécie apresenta número cromossômico mitótico 2n = 40 com comprimento cromossômico geral médio de 1,042 µm ± 0,140 e amplitude variando de 0,58 µm até 1,60 µm.
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Um piquete de capim-colonião (Panicum maximum Jacq) submetido a pastoreio contínuo e a roçadas periódicas revelou, seis anos após o plantio, elevado grau de infestação por outras plantas, destacando-se entre elas a grama-batatais (Paspalum notatum Flügge) que apresentou 85% de frequência e 20,9% de biomassa epígea seca relativa. As dicotiledóneas, em conjunto, apresentaram frequência de 95% e biomassa relativa de 38,7% mas a sua contribuição específica foi muito reduzida. O capim-colonião, por sua vez, apesar da frequência de 95%, apresentou apenas 32,2% de biomassa relativa (diminuição de 67,8%). Estas profundas alterações da flora e da vegetação podem ser atribuidas, em grande parte, a dois fatores: a) ação seletiva da roçadeira; b) preferências alimentares e disseminação endozoócora da gramabatatais pelos bovinos.
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Uma população de Porophyllum ruderale (Jacq.) Cass. ocorrente nos arredores de São José do Rio Preto (SP) foi estudada quanto à estatura, biomassa epígea seca, número de ramos, de capítulos por ramo e por indivíduo e quanto à produção de aquênios por capítulo e por indivíduo. Esta última foi relativamente baixa (média de 2510 aquênios) correspondendo, na base de 80% de germinabilidade, à média de 2008 disseminulos viáveis por indivíduo. Esta capacidade reprodutiva é muito superior ao número de indivíduos que habitualmente ocorrem em condições naturais. A fraca densidade populacional característica da espécie deve ser atribuída, portanto, a outros fatores, tais como, possivelmente, as condições do solo, a competição interespecífica e, talvez, a ação de inimigos naturais. A produção individual de capítulos e de aquênios revelou correlação com a estatura e a biomassa mas o número de aquênios por capítulo (53 em média) não revelou correlação com a estatura, a biomassa e a produção individual de capítulos e de aquénios, demonstrando ser um carater pouco afetado pelo vigor vegetativo.
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Seeds of Aechmea bromeliifolia, A. castelnavii (Bromelioideae); Dyckia duckei, D. racemosa (Pitcairnioideae) and Tillandsia adpressiflora (Tillandsioideae) were collected in the Amazon regions (Mato Grosso) and studied to describe morphological characterization and post-seminal development, which can be taxonomically useful, and to assess percent germination. All the species have epigeous germination and produce cryptocotyledonary plantlets. Seeds have no dormancy and percent germination is high (over 86%), which facilitates the production of seedlings and conservation studies. Exclusive characteristics of the genera include: the seed coat of Aechmea (Bromelioideae) has mucilage that prevents desiccation; whereas that of Dyckia (Pitcairnioideae) has membranaceous wings and that of Tillandsia (Tillandsioideae) has feathery appendages, both of which make dispersal easier and establish the epiphytic habit. Initial post-seminal development of Aechmea (Bromelioideae) and Dyckia (Pitcairnioideae) is marked by the emergence of primary roots, interpreted as a basal character, whereas that of Tillandsia adpressiflora (Tillandsioideae) is marked by the emergence of the cotyledon, interpreted as a derived character. Dyckia and Tillandsia have a small tank only in the seedling phase while the contrary occurs in Aechmea.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
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Elephant grass and castor cake when combined can make a promising organic fertilizer. However, castor cake contains potentially toxic chemicals, such as ricin and ricinine. To test potential effects of these chemicals, compost piles of elephant grass ( Pennisetum purpureum Schum.) with castor cake were prepared with different C:N ratios (T1 = 40, T2 = 30, T3 = 20; T4 = 30 [control, elephant grass + crotalaria]) to evaluate colonization by edaphic fauna and any suppressive effects of castor cake. Soil organisms were collected with Berlese-Tullgren funnels. There were temporal differences between the treatments, and the epigeous fauna was mainly represented by members of the Acari and Entomobryomorpha. Elapsed time is the major factor in determining the composition of the epigeous fauna community associated with composting, indicating that castor cake has no suppressive effect.