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Community ecologists have attempted to explain species abundance distribution (SAD) shape for more than 80 years, but usually without relating SAD shape explicitly to ecological variables. We explored whether the scale (total assemblage abundance) and shape (assemblage evenness) of avifaunal SADs were related to ecological covariates. We used data on avifaunas, in-site habitat structure and landscape context that were assembled from previous studies; this amounted to 197 transects distributed across 16,000 km of the box-ironbark forests of southeastern Australia. We used Bayesian conditional autoregressive models to link SAD scale and shape to these ecological covariates. Variation in SAD scale was relatable to some ecological covariates, especially to landscape vegetation cover and to tree height. We could not find any relationships between SAD shape and ecological covariates. SAD shape, the core component in SAD theory, may hold little information about how assemblages are governed ecologically and may result from statistical processes, which, if general, would indicate that SAD shape is not useful for distinguishing among theories of assemblage structure. [ABSTRACT FROM AUTHOR]

Elevational patterns of species richness, local abundance and assemblage structure of rainforest birds of north-eastern Australia were explored using data from extensive standardized surveys throughout the region. Eighty-two species of birds were recorded with strong turnover in assemblage structure across the elevational gradient and high levels of regional endemism in the uplands. Both species richness and bird abundance exhibited a humped-shaped pattern with elevation with the highest values being between 600 and 800 m elevation. While much of the variability in species richness could be explained by the species–area relationship, analyses of net primary productivity (NPP) and total daily energy consumption of the bird community (energy use) suggest that ecosystem energy flow or constraints may be a significant determinant of species richness. Species richness is positively correlated with local bird abundance which itself is closely related to total energy use of the bird community. We suggest the hypothesis that lower NPP limits bird abundance and energy use in the uplands (>500 m) and that low bird energy use and species richness in the lowlands is limited by a seasonal bottleneck in available primary productivity and/or a species pool previously truncated by an extinction filter imposed by the almost complete disappearance of rainforest in the lowlands during the glacial maxima. We suggest that some of the previously predicted impacts of global warming on biodiversity in the uplands may be partially ameliorated by increases in NPP because of increasing temperatures. However, these relationships are complex and require further data specifically in regard to direct estimates of primary productivity and detailed estimates of energy flow within the assemblage. [ABSTRACT FROM AUTHOR]

The article presents a study which examines the dynamics of fish assembly structure of fish fauna in natural and constructed estuarine lakes in Australia. The study uses multivariate classification and regression trees (mCARTs) to determine the assemblage structure of the estuaries samples collected from November 2007 and January 2009. The result shows that the fish assemblage of the natural estuaries has consistent patterns of temporal change while the constructed estuarine lakes have low absolute probability of encounters (PoEs). It adds that offshore spawning species using estuaries as a nursery ground are the main contributors for the temporal differences in assemblage structure.

Coral reefs are under increasing pressure from a variety of stressors, highlighting the need for information about the status of coral reef communities including the distribution, abundance and composition of juvenile and adult coral assemblages. This information is currently limited for the Great Barrier Reef (GBR) and is necessary for understanding the impacts of disturbances and the system's potential for recovery. This study reports juvenile and adult hard coral abundance and composition from 122 reefs on the GBR during a period of limited acute disturbance. The data represent baseline observations for juvenile hard coral assemblages spanning the longitudinal cross-shelf gradient of the GBR and 12 degrees of latitude and augment reported distribution of adult coral assemblages over the same scale with inclusion of additional reefs. Juvenile and adult coral assemblages reflected broad differences imposed by the gradient of environmental conditions across the GBR. The mean density of juvenile hard corals was lower in the inshore reefs (5.51 m2) than at either the mid-shelf (11.8 m2) or outer shelf reefs (11.2 m2). The composition of juvenile and adult coral assemblages covaried overall, although there were different relationships between these two life stages across the continental shelf and among community types. Dissimilarity between juvenile and adult coral assemblages was greater on inshore and outer shelf reefs than on reefs in the mid-shelf, although, there were differences in community types both within these shelf positions and those that spanned mid- and outer shelf reefs. Dissimilarity was greatest for Inshore branching Acropora and high for Southern Acropora communities, although very high coral cover and very low juvenile densities at these reefs precluded interpretation beyond the clear competitive dominance of Acropora on those reefs. Dissimilarity was also high between juvenile and adult coral assemblages of Turbid inshore communities suggesting water quality pressures, along with synergistic effects of other stressors, pose ongoing selective pressures beyond the juvenile stage. Conversely, relatively low dissimilarity between juvenile and adult coral assemblages on mid-shelf and lower latitude outer shelf reefs suggests pressures beyond those influencing settlement and early post-settlement survival were having less influence on the composition of adult coral assemblages. [ABSTRACT FROM AUTHOR]