Many studies suggest that edaphic variables are major determinants of frog distributions. However, leaf-litter depth and soil characteristics are influenced by distance from streams, so the apparent relationship between edaphic characteristics and species distributions could be an artefact of the dependence of species on free water for reproduction. Therefore, we investigated the effect of edaphic variables on the mesoscale distribution of frog species not dependent on free water for reproduction. We evaluated the effects of soil texture, pH, slope, number of trees and leaf-litter volume on the distribution of nine terrestrially reproducing anuran species in the Reserva Ducke, a 100-km2 terra firme forest preserve in central Amazonia. Diurnal and nocturnal assemblages of anuran species were sampled in 72 plots systematically distributed across the reserve. We sampled the diurnal anuran assemblage by visual encounter in 250 × 1-m plots and the nocturnal assemblage in 250 × 20-m plots using both auditory and visual surveys. The majority of terrestrially breeding anuran species were influenced by topographic and/or edaphic variables, such as slope, soil clay content and pH. However, responses to environmental predictors differed among species. Most species occurred throughout all environmental gradients and relationships with soil characteristics were subtle, indicating that these species occur in the majority of habitats in Reserva Ducke. The results of this study indicate that terrestrially breeding frogs are habitat generalists that show little mesoscale beta diversity associated with habitat variation.
Predation on amphibians by spiders (Arachnida, Araneae) in the Neotropical region. Herein, we report observations about spider predation on anurans (adults and juveniles) in Central Amazonia and a literature review of spiders preying on amphibians in the Neotropical zoogeographic realm. We conducted field observations in Reserva Florestal Adolpho Ducke, Manaus, AM, and observed eight predation events on Bufonidae, Dendrobatidae, Hylidae, and Leptodactylidae frogs. The predators belong to the spider families Ctenidae, Pisauridae and Theraphosidae. Besides the families of spiders found in this study, two others-Lycosidae and Sparissidae-were found in literature. Frogs from families Centrolenidae and Microhylidae, and a caecilian (Gymnophiona, Caeciliidae) were found in literature also. There is a significant correlation between the length of the anuran (snout-vent length) and the length of spiders (cephalotorax and abdomen length). The size of the spider is similar or slightly lesser than the anuran prey. In general, the spiders preyed on adult and juvenile frogs in the breeding season. Spiders are opportunistic predators and prey on small frogs. Theraphosidae prey upon sub adults of large anurans and caecilians. As spiders can reach high densities on the forest floor-especially species of the genera Ctenus and Ancylometes-this interaction may be ecologically important for breeding anurans. Our reports and literature data provide evidence that spiders commonly prey on amphibians in Neotropic, but the impact of predation on populations of amphibians is unknown.
This study aimed to evaluate if anuran species distributions in riparian and non‐riparian areas are influenced by environmental factors (i.e. niche) and/or by spatial factors (i.e. dispersal). The environmental variables analysed were altitude, distance from the stream and leaf litter depth. Spatial factors were represented by the eigenvectors extracted from geographical coordinates by eigenfunction analysis. The study was conducted in 24 km2 of terra‐firme forest in Central Amazonia, Manaus – Amazonas, Brazil. Between November 2008 and May 2009, three samples were taken from 41 plots, 21 plots being placed at non‐riparian areas and another 20 placed in riparian areas. We submitted the assemblage dataset to a partial redundancy analysis to evaluate the contributions of environmental and spatial variables (selected with a forward selection procedure). In addition, we tested if communities differ from riparian and non‐riparian areas using a db‐MANOVA. Species richness and species composition differed between riparian and non‐riparian plots. Some species were restricted to riparian areas. Altitude was the only significant variable (P = 0.005) explaining 21% of the total variance. When analysing the data from all plots using the partial redundancy analysis, 27% of the variance was explained by spatial and environmental variables. The environmental variables explained exclusively 4% of the variance in assemblage composition, and 13% was explained by environmental variables that were also structured in space (i.e. the shared fraction), while 10% was explained exclusively by spatial variables. In conclusion, our results showed differences between the assemblages of riparian and non‐riparian areas which can be explained by the distribution of anuran species along environmental gradients altitude and distance to streams, with little evidence of dispersal limitation.
The presence of maggots of the fly Beckeriella niger (Ephydridae) in nests of six syntopic South American leptodactyline frogs is reported. The number of tadpoles of Physalaemus cuvieri leaving infested and non-infested nests were compared, and behavioural plasticity at the time of nest departure in the presence and absence of maggots was tested for. Maggots were found in nests of all species with exposed foam nests (four Physalaemus and two Leptodactylus species). The maggots remained in the nests of P. cuvieri for up to 3 days; adults emerged from pupae after 7 days. While in the nests the maggots consumed eggs, embryos, and tadpoles. The levels of infestation increased from the beginning to the middle of the rainy season. Mortality caused by the maggots represented an important source of mortality (mean 74%) of eggs and embryos of P. cuvieri, and probably, of the other species. The time of emergence from nests by the tadpoles of P. cuvieri was shorter (up to 21 h earlier) in infested nests. The tadpoles that left the infested nests were at the same, or a less-developed stage than tadpoles in non-infested nests. The variation in the degree of infestation, with lower values at the beginning and the increase to the middle of the rainy season, suggests that the flies may be an obligatory predator on foam nests. For tadpoles of P. cuvieri, entering the water at a later developmental stage may be important to avoid aquatic predators. Conversely, leaving infested nests at the earliest possible stage may represent a strategy to avoid maggot predation. The longer time before emergence of tadpoles of P. cuvieri from non-infested nests corroborates the hypothesis that, among leptodactyline frogs, the foam nest is a predator avoidance adaptation in the aquatic media.
ABSTRACT. The objectives of this study were to measure and compare niche breadth and overlap of males of Hyla nana Boulenger, 1889 and Hyla sanborni Schmidt, 1944 in three neighboring ponds. The measured niche dimensions were seasonal occurrence, call site, and diet. The reproductive season of H. sanborni was longer in permanent ponds, whereas H. nana had a longer reproductive season in the temporary pond. Call site characteristics were similar for both species, however H. sanborni called from higher perches than H. nana. Diptera (Nematocera) were the most consumed item by both species in the three ponds but, in general, H. nana ingested larger prey than H. sanborni. For both species, the consumption of prey types was correlated with the availability in the environment. The multidimensional overlap between H. nana and H. sanborni was higher in the permanent ponds than the temporary pond, in which H. sanborni was rare. These species differed in abundance among ponds, consumed prey of different sizes, and probably fed in different time periods. Moreover, the data obtained suggest that structural differences in the ponds may modify the dynamics of resource partitioning between the two species. Beside the great overlap found in the major niche dimensions analyzed the detected differences may be great enough to allow their coexistence. KEY WORDS. Hyla, multidimensional overlap, niche breadth, niche overlap, resource partitioning.
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