12 research outputs found

    Mixed effects of habitat fragmentation on species richness and community structure in a microarthropod microecosystem

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    1. Theory is unclear about the optimal degree of isolation of habitat fragments where the aim is to maximise species richness. In a field-based microecosystem of Collembola and predatory and non-predatory mites, moss patches of the same total area were fragmented to varying degrees. The habitat was left for several months to allow the communities to approach a new state of equilibrium. 2. The species richness (in particular of predatory mites) of a given area of habitat was greater when it was part of a large mainland area than part of an island, in agreement with theory. 3. Conversely, species richness and abundance were largely unaffected by fragmentation of a fixed area of island habitat. In this case, it is suggested here that the advantages of several small patches (e.g. reduced impact of environmental stochasticity, wider range of habitats overall) were equally balanced by the advantages of a single large patch (e.g. reduced effect of demographic stochasticity, wider range of habitats within a single patch, reduced edge effect), or that both effects were small. 4. The shapes of rank-abundance curves were similar among the levels of fragmentation of a fixed area of island habitat, implying that fragmentation had little impact on community structure. Conversely, the species composition of non-predatory mites varied weakly, but significantly, by fragmentation

    Bird Responses at Inherent and Induced Edges in the Murray Mallee, South Australia. 2. Nest predation as an Edge Effect

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    We assayed nest predation as an edge effect, using artificial ground nests, at inherent (naturally occurring) and induced (human-created) edges in the Murray Mallee, South Australia. Nests were constructed at distances between 0-120 m away from habitat edges. The relative predation rate on nests generally increased close to induced edges with a significant difference (P < 0.05) recorded for two out of five experiments. Predation rate at inherent edges was similar from the edge to the interior, and was lower than that recorded at induced edges. Our results suggest that increased predator numbers, activity or efficiency at locating nests occurred close to the induced edges at our study sites

    Predação de ninhos artificiais em uma ilha na Mata Atlântica: testando o local e o tipo de ovo Artificial nest predation in Atlantic Forest Island: testing the place and the different types of egg

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    Experimentos com ninhos artificiais são utilizados para testar hipóteses ecológicas e comportamentais que influenciam na predação de ninhos naturais. O tamanho do ovo, a textura da casca e a cor podem influenciar na taxa de predação, porém poucos estudos avaliam qual modelo de ovo é o mais adequado para simular a predação de ninhos em áreas tropicais. O objetivo deste trabalho foi comparar a predação de diferentes modelos de ovos (ovos de codorna, massa de modelar e canários) no solo e a 1,30 m de altura no sub-bosque. O experimento foi realizado Ilha Anchieta, Ubatuba, São Paulo, Brasil. Foi encontrada uma diferença significativa na taxa de predação entre os ovos de codorna (71,87%) e sintéticos (93,75%) e entre os ovos de codorna e de canário (100%) no solo. Entretanto, não houve diferença significativa entre os ovos sintéticos e de canário. Os ninhos no sub-bosque apresentaram um padrão diferenciado do solo quando se refere aos ovos de codorna (25%) e sintéticos (28,1%), mas houve diferenças significativas quando os ovos de canário foram comparados com os ovos sintéticos e de codorna. Nosso trabalho demonstrou que diferentes tipos de ovos sobre uma mesma pressão de mesopredadores apresentaram taxas de predação diferentes. Portanto, estudos que avaliam o sucesso reprodutivo da avifauna baseado na predação de ninhos artificiais devem considerar a utilização de diferentes tipos de ovos e estratos na vegetação.<br>Experiments on artificial nests are usually used to test ecological hypothesis and behavioural that affects the predation of natural bird nests. It is has been discussed about the size of the egg, texture and color affecting predation rate, but a few studies evaluate which egg type is more appropriate to simulate nest predation in tropical areas. The objective of this work was to compare the predation of different models of eggs (Coturnix coturnix, plasticine and Serinus canarius) on the ground and understory in a island with high abundance of nest predators. The study was carry out in October 2004 at Anchieta Island, Ubatuba, São Paulo, Brazil. The nests on the ground showed a statistical significance difference in the predation of quail eggs, plasticine and canary eggs. However, we did not find differences between plasticine and canaries eggs. The nests in the understory had a different pattern on the ground of quail eggs (25%) and plasticine (28%) and there was a difference when we compare canary eggs with plasticine and quail eggs. Our work pointed out that different eggs may have different predation rates. Therefore, studies that evaluate reproductive fitness of the bird community based on artificial nests must considered different egg types and strata

    A simple mechanistic model of seed dispersal, predation and plant establishment: Janzen-Connell and beyond

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    1. Although, in nature, seed dispersal usually declines with distance from the source, seedling establishment patterns are highly variable. An increase in seed survival can lead to either hump-shaped (Janzen-Connell (J-C) pattern) or declining (Hubbell pattern) establishment with distance from seed source, but declining establishment can also be generated if survival decreases with distance (McCanny pattern). Pathogens and seed predators are considered to be major mortality agents structuring recruitment patterns, but it is unclear how well predation alone can explain variation in these patterns. 2. We introduce a simple mechanistic model showing that distance and density-dependent seed predation can generate all of the observed recruitment patterns. Our approach provides the first mathematical reconstruction of conceptual models previously considered to be based on contrasting underlying mechanisms. Three easily measurable quantities (the proportion of seeds escaping predation at the source, and the mean distance from the source of dispersed seeds and of predators’ activity) can be used to test for consistency with the J-C pattern. The association between recruitment patterns and plant (dispersal) and animal (predation) characteristics is robust with respect to parameter values and various functional forms. 3. The model shows that the J-C pattern can occur only if the mean distance over which predators are active is lower than that over which seeds are dispersed, corresponding to a system with host-specific, or immobile, seed predators (often invertebrates) that are restricted to areas of high seed density near adult plants, and therefore selecting for longer dispersal distances of seeds. 4.The Hubbell pattern is generated by the model when dispersal and predation distances are of equivalent magnitudes. The McCanny pattern emerges if more generalized, or more mobile, seed predators (often vertebrates) are attracted to the adult trees but also tend to forage farther away, thereby selecting for short dispersal distances that generate high densities needed to satiate seed predators. 5.The model also predicts that the total number of seeds surviving predation is lowest at intermediate distances, suggesting that distance-dependent predation promotes either short or long dispersal distances, or both (dimorphism)
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