Tobin D. Northfield

Organic agriculture promotes evenness and natural pest control

Human activity can degrade ecosystem function by reducing species number (richness) and by skewing the relative abundance of species (evenness). Conservation efforts often focus on restoring or maintaining species number, reflecting the well-known impacts of richness on many ecological processes. In contrast, the ecological effects of disrupted evenness have received far less attention, and developing strategies for restoring evenness remains a conceptual challenge. In farmlands, agricultural pest-management practices often lead to altered food web structure and communities dominated by a few common species, which together contribute to pest outbreaks. Here we show that organic farming methods mitigate this ecological damage by promoting evenness among natural enemies. In field enclosures, very even communities of predator and pathogen biological control agents, typical of organic farms, exerted the strongest pest control and yielded the largest plants. In contrast, pest densities were high and plant biomass was low when enemy evenness was disrupted, as is typical under conventional management. Our results were independent of the numerically dominant predator or pathogen species, and so resulted from evenness itself. Moreover, evenness effects among natural enemy groups were independent and complementary. Our results strengthen the argument that rejuvenation of ecosystem function requires restoration of species evenness, rather than just richness. Organic farming potentially offers a means of returning functional evenness to ecosystems.

Spatiotemporal Patterns and Dispersal of Stink Bugs (Heteroptera: Pentatomidae) in Peanut-Cotton Farmscapes

ABSTRACT In the southeast United States, a field of peanuts, Arachis hypogaea L., is often closely associated with a field of cotton, Gossypium hirsutum L. The objective of this 4-yr on-farm study was to examine and compare the spatiotemporal patterns and dispersal of the southern green stink bug, Nezara viridula L., and the brown stink bug, Euschistus servus (Say), in six of these peanut-cotton farmscapes. GS+ Version 9 was used to generate interpolated estimates of stink bug density by inverse distance weighting. Interpolated stink bug population raster maps were constructed using ArcMap Version 9.2. This technique was used to show any change in distribution of stink bugs in the farmscape over time. SADIE (spatial analysis by distance indices) methodology was used to examine spatial aggregation of individual stink bug species and spatial association of the two stink bug species in the individual crops. Altogether, the spatiotemporal analyses for the farmscapes showed that some N. viridula and E. servus nymphs and adults that develop in peanuts disperse into cotton. When these stink bugs disperse from peanuts into cotton, they aggregate in cotton at the interface, or common boundary, of the two crops while feeding on cotton bolls. Therefore, there is a pronounced edge effect observed in the distribution of stink bugs as they colonize the new crop, cotton. The driving force for the spatiotemporal distribution and dispersal of both stink bug species in peanut-cotton farmscapes seems to be availability of food in time and space mitigated by landscape structure. Thus, an understanding of farmscape ecology of stink bugs and their natural enemies is necessary to strategically place, in time and space, biologically based management strategies that control stink bug populations while conserving natural enemies and the environment and reducing off-farm inputs.

Niche saturation reveals resource partitioning among consumers

More diverse communities of consumers typically use more resources, which often is attributed to resource partitioning. However, experimentally demonstrating this role of resource partitioning in diverse communities has been difficult. We used an experimental response-surface design, varying intra- and interspecific consumer densities, to compare patterns of resource exploitation between simple and diverse communities of aphid predators. With increasing density, each single consumer species rapidly plateaued in its ability to extract more resources. This suggests intraspecific competition for a subset of the resource pool, a hallmark of resource partitioning. In contrast, more diverse-predator communities achieved greater overall resource depletion. By statistically fitting mechanistic models to the data, we demonstrated that resource partitioning rather than facilitation provides the better explanation for the observed differences in resource use between simple and diverse communities. This model-fitting approach also allowed us to quantify overlap in resource use by different consumer species.

Annual Cycles of Frankliniella spp. (Thysanoptera: Thripidae) Thrips Abundance on North Florida Uncultivated Reproductive Hosts: Predicting Possible Sources of Pest Outbreaks

Abstract Frankliniella spp. (Thysanoptera: Thripidae) thrips damage a variety of crops, feed on a broad range of hosts, and often migrate into cropping systems from adjacent vegetation. To determine potential sources of Frankliniella spp. thrips on crops, annual cycles of abundance of Frankliniella occidentalis (Pergande), Frankliniella fusca (Hinds), Frankliniella bispinosa (Morgan), and Frankliniella tritici (Fitch) were evaluated on seven common, uncultivated reproductive hosts. These hosts included Raphanus raphanistrum L., Rubus trivialis Michx., Rubus cuneifolius Pursh., Vicia sativa L., Trifolium repens L., Solidago canadensis L. and Chenopodium ambrosioides L. Thrips were collected from R. cuneifolius, and T. repens in the spring, R. raphanistrum in the summer, and C. ambrosioides and S. canadensis in the fall. The most common Frankliniella species on every plant species was F. tritici, and a fifth species, Pseudothrips inequalis (Beach), was collected in the fall on C. ambrosioides and S. canadensis. All thrips species were highly aggregated in the flowers or flower racemes, rather than leaves or fruit, and they were generally only collected from flowering plants. R. raphanistrum supported large populations, and they may be an important link for thrips between spring and fall. In addition, it may be an essentially enemy free host, as only one O. insidiosus, an important thrips predator, was collected from this host. S. canadensis also supported large thrips populations in the fall, and it may be a source of thrips migrating into crops the following spring. Controlling thrips on these hosts in their respective seasons may limit the number migrating into cropping systems.

Behavioral Model for Homalodisca vitripennis (Hemiptera: Cicadellidae): Optimization of Host Plant Utilization and Management Implications

The glassy-winged sharpshooter, Homalodisca vitripennis (Germar), (Hemiptera: Cicadellidae), is a xylophagous leafhopper native to the southeastern United States and northern Mexico, with recent introductions into California, Arizona, French Polynesia, and Hawaii. It is a primary vector of the xylem-limited bacterium, Xylella fastidiosa Wells et al., the causative agent of Pierce’s disease of grape, citrus variegated chlorosis, phony peach, and numerous leaf scorch diseases. H. vitripennis uses several hundred species of host plants for feeding, development, and reproduction. Variation in host utilization allows H. vitripennis to respond to diurnal and seasonal changes in its nutrient-poor food source, xylem fluid, as well as changing nutritional requirements of each leafhopper developmental stage. Here we provide a conceptual model that integrates behavior, life history strategies, and their associated risks with the nutritional requirements of adult and nymphal stages of H. vitripennis. The model is a useful heuristic tool that explains patterns of host plant use, describes insect behavior and ecology, suggests new associations among the ecological components, and most importantly, identifies and supports the development of suppression strategies for X. fastidiosa aimed at reducing vector populations through habitat manipulation.

Conserving and promoting evenness: organic farming and fire-based wildland management as case studies

Healthy ecosystems include many species (high richness) with similar abundances (high evenness). Thus, both aspects of biodiversity are worthy of conservation. Simultaneously conserving richness and evenness might be difficult, however, if, for example, the restoration of previously absent species to low densities brings a cost in reduced evenness. Using meta-analysis, we searched for benefits to biodiversity following adoption of two common land-management schemes: the implementation of organic practices by farmers and of controlled burning by natural-land managers. We used rarefaction to eliminate sampling bias in all of our estimates of richness and evenness. Both conservation practices significantly increased evenness and overall abundance across taxonomic classifications (arthropods, birds, non-bird vertebrates, plants, soil organisms). Evenness and richness varied independently, leading to no richness-evenness correlation and no significant overall change in richness. Demonstrating the importance of rarefaction, analyses of raw data that did not receive rarefaction indicated misleadingly strong benefits of organic agriculture and burning for richness while underestimating true gains in evenness. Both organic farming and burning favored species that were not numerically dominant, re-balancing communities as uncommon species gained individuals. Our results support the assertion that richness and evenness capture separate facets of biodiversity, each needing individual attention during conservation.

Within plant interspecific competition does not limit the highly invasive thrips, Frankliniella occidentalis in Florida.

1. Species invasions are often linked to reductions in biodiversity, and competitive superiority is often cited as the main reason for the success of an invasive species. Although invaded ecosystems are often examined, few have studied areas in which an invasive species has failed to successfully invade.

Natural enemy functional identity, trait-mediated interactions and biological control

Recent yearshave seen great interest in the importance of species richness for the functioning and stability of ecological communities (Ives and Carpenter 2007). Empirical examinations of richness effects typically vary the number of species in experimental treatments and measure resulting ecosystem functions such as biomass accumulation or resource uptake (Naeem et al. 2009). Across trophic levels and communities of many types, a clear pattern has emerged from these experiments: community processes (biomass accumulation, resource uptake, etc.) generally become more efficient when more species are present (Hooper et al. 2005; Cardinale et al. 2006). This pattern is generally attributed to resource partitioning among species, where species differ in ecologically significant ways such that they complement one another (Hooper et al. 2005). For example, in English meadow communities multiple plant species coexist, because different plant species exploit different hydrological conditions (Silvertown et al. 1999). The plants that dominate drought-prone areas are different from those that thrive in flood-prone areas and, presumably, total plant biomass is greatest when both plant groups (drought tolerant and flood tolerant) are present.

Does Biodiversity–Ecosystem Function Literature Neglect Tropical Ecosystems?

Current evidence suggests that there is a positive relationship between biodiversity and ecosystem functioning, but few studies have addressed tropical ecosystems where the highest levels of biodiversity occur. We develop two hypotheses for the implications of generalizing from temperate studies to tropical ecosystems, and discuss the need for more tropical research.

Dispersal, Patch Leaving, and Distribution of Homalodisca vitripennis (Hemiptera: Cicadellidae)

ABSTRACT Homalodisca vitripennis (Germar) and related species have caused millions of dollars in damage to southern California vineyards in recent years through the vectoring of Pierces disease. However, the effects of surrounding vegetation on the dispersal and distribution of H. vitripennis are poorly understood. Therefore, the relationship between dispersal rates and patch quality was tested, as well as the basic predictions of the marginal value theorem. Additional experiments were conducted to compare the H. vitripennis distribution in an isolated crape myrtle (Lagerstroemia indica) patch and a L. indica patch bordering two alternative host patches. In mark-release-recapture tests, H. vitripennis dispersed farther from the release point in a patch of low-quality host plants (Prunus persica) than in patches of high-quality host plants (L. indica). In addition, H. vitripennis remained in L. indica patches longer than in P. persica patches and adjusted patch residence times in P. persica in correlation with known changes in plant physiology. These data suggest that H. vitripennis follows the basic predictions of marginal value theorem. In distribution tests, H. vitripennis were more abundant in the patch center than patch edges in the isolated L. indica patch, but in a patch bordering cottonwood (Populus sp.) and peach (P. persica), H. vitripennis numbers were generally higher along the edges of the patch. These data suggest that alternate hosts bordering cropping systems may be important to the spatial dynamics of H. vitripennis. Implications of these spatial observations on the biology of H. vitripennis and potential control methods are discussed.