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 onsite 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.

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.

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.

The latitudinal diversity gradient is the largest scale, and longest known, pattern in ecology. We examined the applicability of three versions of the energy hypothesis, the habitat heterogeneity hypothesis, and historical contingency to the gradient of terrestrial birds. The productivity version of the energy hypothesis, tested using actual evapotranspiration, a water-energy variable closely associated with plant productivity, accounted for 72% of the variance in a model of global extent. An historical contingency model based on biogeographic region explained 58% of the variance. A combined climate-region model accounted for 78% of the variance, but 52% comprised the overlap between these effects. This suggests that further resolution of contemporary vs. historical processes at the global level will require the inclusion of phylogenetic information.Regional-extent regression models suggest a latitudinal shift in constraints on diversity; measures of ambient energy (potential evapotranspiration and mean annual temperature) best predicted the diversity gradient at high latitudes, whereas water-related variables (actual evapotranspiration and annual rainfall) best predicted richness in low-latitude, high-energy regions. Intraregional spatial autocorrelation analysis confirmed that climatic models adequately describe geographic richness patterns at all but the smallest spatial scales resolved by the analysis. We conclude that the "water-energy dynamics" hypothesis, originally developed for plant diversity gradients, offers a parsimonious explanation for bird diversity patterns as well, presumably operating via plant productivity. However, more refined tests of historical factors are needed to fully resolve their influences on the gradient.

There is a well documented relationship between parasitoid species assemblage size and host feeding niche. Parasitoid assemblage size peaks on hosts thought to have intermediate levels of physical refuge. We examined the influence of refuges on parasitoid coexistence using pairs of specialist parasitoids in a controlled laboratory environment. Using physical barriers we excluded parasitoids from 0, 25, 50 or 75% of the hosts to simulate host refuge. We found no evidence that host refuges can promote parasitoid coexistence in a simplified laboratory environment. Results were similar whether pairs of parasitoid species were competitively disparate or competitively similar. Our results suggest that spatial heterogeneity in parasitoid attack rate was not sufficient to maintain parasitoid coexistence regardless of host refuge, and we argue that the level of spatial heterogeneity necessary to promote coexistence is rare in nature. We conclude that in most systems the coexistence of specialist parasitoids cannot be explained by a host refuge effect.

Models of host–parasitoid dynamics often assume constant levels of spatial heterogeneity in parasitoid attack rate, which tends to stabilize the interactions. Recently, authors have questioned this assumption and shown that outcomes of simple host–parasitoid models change if spatial heterogeneity is allowed to vary with parasitoid density. Here, we allow spatial heterogeneity to vary with either parasitoid density or percent parasitism in a model designed to explain specialist parasitoid coexistence on insect hosts with various levels of refuge. By examining this model we can evaluate the effect of varying spatial heterogeneity on a more complex model in which spatial heterogeneity is not considered the primary determinant of persistence. By modeling communities with one host and two parasitoid species, we show that the probability of species persistence for the competitively inferior parasitoid depends on the assumed relationship between spatial heterogeneity and both parasitoid density and percent parasitism. The probability of parasitoid coexistence is generally lower when spatial heterogeneity varies with parasitoid demographics. We conclude that the conditions for which host refuge promote specialist parasitoid coexistence are less common that proposed by the original model. Finally, we compared a model in which spatial heterogeneity varies with percent parasitism to data from laboratory trials and find a reasonable fit. We conclude that the change in spatial heterogeneity strongly influenced the outcome of the laboratory trials, and we suggest more research is necessary before researchers can assume constant spatial heterogeneity in future models.

ABSTRACTAim To investigate the relative contributions of current vs. historical factors in explaining broad‐scale diversity gradients using a combination of contemporary factors and a quantitative estimate of the temporal accessibility of areas for recolonization created by glacial retreat following the most recent Ice Age.Location The part of the Nearctic region of North America that was covered by ice sheets during the glacial maximum 20 000 BP.Methods We used range maps to estimate the species richness of mammals and terrestrial birds in 48 400 km2 cells. Current conditions in each cell were quantified using seven climatic and topographical variables. Historical conditions were estimated using the number of years before present when an area became exposed as the ice sheets retreated during the post‐Pleistocene climate warming. We attempted to tease apart contemporary and historical effects using multiple regression, partial regression and spatial autocorrelation analysis.Results A measure of current energy inputs, potential evapotranspiration, explained 76–82% of the variance in species richness, but time since deglaciation explained an additional 8–13% of the variance, primarily due to effects operating at large spatial scales. Because of spatial covariation between the historical climates influencing the melting of the ice sheet and current climates, it was not possible to partition their effects fully, but of the independent effects that could be identified, current climate explained two to seven times more variance in richness patterns than age.Main Conclusions Factors acting in the present appear to have the strongest influence on the diversity gradient, but an historical signal persisting at least 13 000 years is still detectable. This has implications for modelling changes in diversity patterns in response to future global warming.

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.

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 United States government has historically used methods of oversight to evaluate the performance of its contract organizations. The method oversight creates unnecessary costs, because both the vendor and the customer are allocating resources to maintain similar or often the same data pools. These methods are effective in that they ensure that the vendor provides a competent product, however, costs, both monetary and time spent, can be reduced significantly by the implementation of performance based contracting (PBC). PBC is predicated on the theory that contractors are responsible for ensuring product quality by offering only conforming products to the aerospace industry. Implementing PBC as a method of maintaining contracts would be greatly beneficial to the customer, because it would put not only the responsibility of data maintenance into the vendors hands, but the direct cost as well. Compliance with ISO standards was found to be an acceptable criterion when evaluating the vendor's capabilities of data maintenance, because ISO standards often determine the desired data to be collected.

We tested the hypothesis that area represents the primary explanation for the latitudinal diversity gradient using breeding terrestrial birds of North America, the northern Palearctic, Australia and the Afrotropics as our focal group. We tested two propositions inherent to the area hypothesis: (1) tropical biomes are larger than extra‐tropical biomes, and (2) there is a significant species‐area relationship for birds at the biome scale of resolution. Using a more realistic definition of biomes which incorporates the effects of both energy and water, we find no support for either proposition, leading us to conclude that the area per se does not explain terrestrial latitudinal diversity gradients.

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.

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.