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Dive into the research topics where Eric E. Porter is active.

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Featured researches published by Eric E. Porter.


Ecology | 2003

Energy, water, and broad-scale geographic patterns of species richness

Bradford A. Hawkins; Richard Field; Howard V. Cornell; David J. Currie; Jean François Guégan; Dawn M. Kaufman; Jeremy T. Kerr; Gary G. Mittelbach; Thierry Oberdorff; Eileen M. O'Brien; Eric E. Porter; John R. G. Turner

It is often claimed that we do not understand the forces driving the global diversity gradient. However, an extensive literature suggests that contemporary climate constrains terrestrial taxonomic richness over broad geographic extents. Here, we review the empirical literature to examine the nature and form of the relationship between climate and richness. Our goals were to document the support for the climatically based energy hypothesis, and within the constraints imposed by correlative analyses, to evaluate two versions of the hypothesis: the productivity and ambient energy hypotheses. Focusing on studies extending over 800 km, we found that measures of energy, water, or water-energy balance explain spatial variation in richness better than other climatic and non-climatic variables in 82 of 85 cases. Even when considered individually and in isolation, water/ energy variables explain on average over 60% of the variation in the richness of a wide range of plant and animal groups. Further, water variables usually represent the strongest predictors in the tropics, subtropics, and warm temperate zones, whereas energy variables (for animals) or water-energy variables (for plants) dominate in high latitudes. We conclude that the interaction between water and energy, either directly or indirectly (via plant productivity), provides a strong explanation for globally extensive plant and animal diversity gradients, but for animals there also is a latitudinal shift in the relative importance of ambient energy vs. water moving from the poles to the equator. Although contemporary climate is not the only factor influencing species richness and may not explain the diversity pattern for all taxonomic groups, it is clear that understanding water-energy dynamics is critical to future biodiversity research. Analyses that do not include water-energy variables are missing a key component for explaining broad-scale patterns of diversity.


The American Naturalist | 2003

Does herbivore diversity depend on plant diversity? The case of California butterflies

Bradford A. Hawkins; Eric E. Porter

It is widely believed that the diversity of plants influences the diversity of animals, and this should be particularly true of herbivores. We examine this supposition at a moderate spatial extent by comparing the richness patterns of the 217 butterfly species resident in California to those of plants, including all 5,902 vascular plant species and the 552 species known to be fed on by caterpillars. We also examine the relationships between plant/butterfly richness and 20 environmental variables. We found that although plant and butterfly diversities are positively correlated, multiple regression, path models, and spatial analysis indicate that once primary productivity (estimated by a water‐energy variable, actual evapotranspiration) and topographical variability are incorporated into models, neither measure of plant richness has any relationship with butterfly richness. To examine whether butterflies with the most specialized diets follow the pattern found across all butterflies, we repeated the analyses for 37 species of strict monophages and their food plants and found that plant and butterfly richness were similarly weakly associated after incorporating the environmental variables. We conclude that plant diversity does not directly influence butterfly diversity but that both are probably responding to similar environmental factors.


Ecological Entomology | 2003

Water–energy balance and the geographic pattern of species richness of western Palearctic butterflies

Bradford A. Hawkins; Eric E. Porter

Abstract.  1. Using two sources of data to estimate butterfly species richness, the potential influences of 11 environmental variables on the richness gradient of butterflies in western/central Europe and northern Africa were examined with multiple regression and spatial autocorrelation analysis. A measure of water–energy balance, actual evapotranspiration, explained 79% of the variance in butterfly species richness using data derived from range maps, and 72% of the variance using data derived from grid‐based distribution maps. All other variables explained less than 4% of the variance in the regression models and differed depending on the data source.


Urban Ecosystems | 2001

Woody vegetation and canopy fragmentation along a forest-to-urban gradient

Eric E. Porter; Brian R. Forschner; Robert B. Blair

To identify patterns that can be used to predict vegetation and landscape characteristics in urban environments, we surveyed the species composition and size of woody plants, as well as the landscape structure of forest canopies, along a forest-to-urban gradient near Oxford, Ohio, USA. The gradient included six sites of increasingly urban land-use: a preserve, a recreational area, a golf course, a residential subdivision, apartment complexes, and a business district. We recorded species identity and stem diameter for all woody plants greater than 3 cm diameter at breast height (DBH) to examine the distribution of individual species as well as overall community composition. We used digitized aerial photographs to compare the spatial characteristics of the forest canopy at each site. We found predictable patterns in species diversity (Shannon index), spatial heterogeneity in species composition (mean percent dissimilarity), and all measures of patch fragmentation (canopy cover and patch number and size). There were clear differences in tree density and total basal area between forested sites and developed sites, but there was little resolution among developed sites. Species richness and average DBH showed no clear pattern, suggesting that landscaping preference largely determined these values. We present a modified version of an intermediate heterogeneity model that can be used to predict diversity patterns in urban areas. We discuss probable mechanisms that led to these patterns and the potential implications for animal communities in urban environments.


The American Naturalist | 2001

Latitudinal Gradients in Colony Size for Social Insects: Termites and Ants Show Different Patterns

Eric E. Porter; Bradford A. Hawkins

On the basis of a comparison of Nearctic and Neotropical ants, social insects have been proposed to show a latitudinal gradient in colony size. Further, the “fasting endurance hypothesis,” which predicts larger colonies in areas with extended periods of low food availability, was proposed as the mechanism driving the gradient. To test the generality of the pattern and its mechanism, we examined the relationships between termite colony size and both latitude and annual evapotranspiration, a measure of plant productivity. We found no evidence that colony size increases with increasing latitude or decreasing plant productivity. We conclude that the pattern identified for ants cannot be generalized to include social insects as a whole. As is the case for ecogeographic gradients in insect body sizes, a pattern that is reported for one taxon may not be consistent for other taxa at the global level.


Wildlife Society Bulletin | 2005

Multiple spatial-scale assessment of the conservation value of golf courses for breeding birds in southwestern Ohio

Eric E. Porter; Jason Bulluck; Robert B. Blair

Abstract Previous work on gradients of human-altered landscapes has identified golf courses as potentially valuable areas for wildlife conservation. We assessed 6 golf courses in and around Oxford, Ohio that were surrounded by varying degrees of land-use intensity and studied bird communities within these courses to identify factors that promote diverse bird assemblages. We used a Geographic Information System (GIS) and aerial photography to estimate percentages of different land-cover types surrounding each course using buffers at scales of 100–1,000 m. We also measured on-site vegetation characteristics within 50 m of the same points used for bird sampling. We used simple linear regressions between each environmental variable and bird community statistics (abundance, species richness, Shannon diversity, and evenness) to determine which variables had the most influence on bird communities. We found that landscapes surrounding golf courses were the most important determinants of bird diversity and on-site variables were relatively unimportant. Specifically, natural land-cover buffers (forests, riparian areas, and open water) promote bird diversity and residential cover reduces diversity, especially in small buffers immediately surrounding courses. Results were similar when we limited the bird data set to Neotropical migrants or to birds with declining population trends.


Oecologia | 1998

Patterns of diversity for aphidiine (Hymenoptera: Braconidae) parasitoid assemblages on aphids (Homoptera)

Eric E. Porter; Bradford A. Hawkins

Abstract We used aphids (Aphidae) as a representative hemimetabolous host family to investigate patterns of parasitoid (Aphidiine) assemblage size. The aphidiine assemblages from 477 aphid species were used to estimate average assemblage size and the influence of eight ecological and taxonomic variables. Aphids species support an average of 1.7 aphidiine species. Aphid subfamily and invasion status (native or exotic) were the most important determinants of parasitoid richness, explaining 28% of the deviance in aphidiine assemblage size. Aphids within the largest aphid subfamily, the Aphidinae, support larger parasitoid assemblages than those in other subfamilies. Parasitoid diversity was also highest on exotic aphid hosts (within the Aphidinae) and on hosts in developed habitats (agricultural or urban), though the latter effect is weak. Patterns related to aphid food plant architecture were influenced by an interaction with aphid invasion status; parasitoid diversity drops with increasing architectural complexity on exotic aphids, whereas the diversities on native aphid hosts are similar on different plant types. Weak effects were also found for aphid food plant alternation (whether or not aphids switch hosts seasonally) and climate (annual range in temperature); alternating aphids support more parasitoids than non-alternating hosts, and parasitoid assemblage size is lowest in warm climates. Taxonomic isolation of aphids at the generic level showed no significant relationship with parasitoid diversity. Finally, in contrast to parasitoid assemblages on holometabolous hosts, sample size effects were weak for aphids, possibly due to the narrow host ranges of aphidiines.


Ecology | 2003

PRODUCTIVITY AND HISTORY AS PREDICTORS OF THE LATITUDINAL DIVERSITY GRADIENT OF TERRESTRIAL BIRDS

Bradford A. Hawkins; Eric E. Porter; José Alexandre Felizola Diniz-Filho


Global Ecology and Biogeography | 2003

Relative influences of current and historical factors on mammal and bird diversity patterns in deglaciated North America

Bradford A. Hawkins; Eric E. Porter


Urban Ecosystems | 2001

Woody vegetation and canopy fragmentation along an urban gradient

Eric E. Porter; B. R. Forschner; Robert B. Blair

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