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.

We evaluated the toxicity of three insecticides (lambda cyhalothrin, spinosad, and S-1812) to the natural enemies Bracon mellitor Say, Cardiochiles nigriceps Viereck, Coleomegilla maculata De Geer, Cotesia marginiventris (Cresson), Geocoris punctipes (Say), and Hippodamia convergens Guérin-Méneville, in topical, residual, and field assays. Lambda cyhalothrin exhibited the greatest toxicity to the natural enemies. In topical toxicity tests, lambda cyhalothrin adversely affected each natural enemy species studied. Residues of lambda cyhalothrin on cotton leaves were toxic to B. mellitor, C. nigriceps, C. maculata, and C. punctipes. Interestingly, residues of this insecticide were not very toxic to C. marginiventris and H. convergens. Geocoris punctipes and C. maculata numbers in the field generally were significantly lower for lambda cyhalothrin treatments than for the other four treatments, substantiating the previous tests. Although cotton aphids began to increase over all treatments around the middle of the test period, the number of cotton aphids in the lambda cyhalothrin plots was significantly higher than the number in any of the other treatments. As cotton aphids increased in lambda cyhalothrin field plots, the predator H. convergens also increased in number, indicating that lambda cyhalothrin did not adversely affect it in accordance with the residual tests. Spinosad exhibited marginal to excellent selectivity, but was highly toxic to each parasitoid species and G. punctipes in topical toxicity tests and to B. mellitor in residual tests. Spinosad generally did not affect the number of G. punctipes, H. convergens, and C. maculata in the field except for one day after the second application for G. punctipes. S-1812 exhibited good to excellent selectivity to the natural enemies. Some reduction of G. punctipes occurred for only a short period after the first and second application of this insecticide in the field. H. convergens and C. maculata were affected very little by S-1812.

Detecting infestations of stink bugs (Heteroptera: Pentatomidae) using pheromones remains problematic, particularly so in the United States for the exotic stink bug, Nezara viridula L., and our native stink bug, Acrosternum hilare (Say). Therefore, we conducted a 2-yr on-farm study to examine the attractiveness and possible cross-attraction of the reported pheromones for N. viridula and A. hilare and those previously discovered for Euschistus servus (Say) and Plautia stali Scott to N. viridula, A. hilare, and E. servus. The attractiveness of selected pentatomid pheromones to tachinid parasitoids of stink bugs was also examined. We showed for the first time under field conditions that N. viridula can be trapped with its reported pheromone, a 3:1 trans- to cis-(Z)-alpha-bisabolene epoxide blend. In fact, attraction of N. viridula increased with higher pheromone doses. Traps baited with a 5:95 trans- to cis-(Z)-alpha-bisabolene epoxide blend, the reported male-produced A. hilare attractant pheromone, failed to attract significantly more A. hilare than did unbaited control traps. Instead A. hilare was significantly cross-attracted to the P. stali pheromone [methyl (E,E,Z)-2,4,6-decatrienoate]. The E. servus pheromone [methyl (E,Z)-2,4-decadienoate], either alone or in combination with P. stali pheromone, was more attractive to E. servus than to N. viridula, P. stali, or A. hilare pheromones. In general, tachinid parasitoids were found responsive to the male-specific volatiles of their known hosts, including the attractiveness of Trichopoda pennipes (F.) to sesquiterpenoid blends characteristic of A. hilare and N. viridula. A tachinid parasitoid of E. servus, Cylindromyia sp., seemed to be attracted to E. servus pheromone. In conclusion, our results indicate that stink bug traps baited with lures containing N. viridula pheromone blend, P. stali pheromone, and E. servus pheromone have the greatest potential for detecting populations of N. viridula, A. hilare, and E. servus, respectively, in diversified agricultural landscapes.

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Brown stink bug, Euschistus servus (Say) (Heteroptera: Pentatomidae), damage on developing corn, Zea mays L., ears was examined in 2005 and 2006 by using eight parameters related to its yield and kernel quality. Stink bug infestations were initiated when the corn plants were at tasseling (VT), mid-silking (R1), and blister (R2) stages by using zero, three, and six in 2005 or zero, one, two, and four bugs per ear in 2006, and maintained for 9 d. The percentage of discolored kernels was affected by stink bug number in both years, but not always affected by plant growth stage. The growth stage effect on the percentage of discolored kernels was significant in 2006, but not in 2005. The percentage of aborted kernels was affected by both stink bug number and plant growth stage in 2005 but not in 2006. Kernel weight was significantly reduced when three E. sercus adults were confined on a corn ear at stage VT or R1 for 9 d in 2005, whereas one or two adults per ear resulted in no kernel weight loss, but four E. servus adults did cause significant kernel weight loss at stage VT in 2006. Stink bug feeding injury at stage R2 did not affect kernel damage, ear weight or grain weight in either year. The infestation duration (9 or 18 d) was positively correlated to the percentage of discolored kernels but did not affect kernel or ear weight. Based on the regression equations between the kernel weight and stink bug number, the gain threshold or economic injury level should be 0.5 bugs per ear for 9 d at stage VT and less for stage R1. This information will be useful in developing management guidelines for stink bugs in field corn during ear formation and early grain filling stages.

In southeastern United States farmscapes, corn, Zea mays L., is often closely associated with peanut, (Arachis hypogaea L.), cotton, (Gossypium hirsutum L.), or both. The objective of this 3-yr on-farm study was to examine the influence of corn on stink bugs (Heteroptera: Pentatomidae), Nezara viridula (L.), and Euschistus servus (Say), in subsequent crops in these farmscapes. Adults of both stink bug species entered corn first, and seasonal occurrence of stink bug eggs, nymphs, and adults indicated that corn was a suitable host plant for adult survival and nymphal development to adults. Stink bug females generally oviposited on cotton or peanut near the interface, or common boundary, of the farmscape before senescence of corn, availability of a new food, or both. Adult stink bugs dispersed from crop to crop at the interface of a farmscape in response to senescence of corn, availability of new food, or both. In corn-cotton farmscapes, adult stink bugs dispersed from senescing corn into cotton to feed on bolls (fruit). In corn-peanut farmscapes, adult stink bugs dispersed from senescing corn into peanut, which apparently played a role in nymphal development in these farmscapes. In the corn-cotton-peanut farmscape, stink bug nymphs and adults dispersed from peanut into cotton in response to newly available food, not senescence of peanut. Stink bug dispersal into cotton resulted in severe boll damage. In conclusion, N. viridula and E. servus are generalist feeders that exhibit edge-mediated dispersal from corn into subsequent adjacent crops in corn-cotton, corn-peanut, and corn-peanut-cotton farmscapes to take advantage of suitable resources available in time and space for oviposition, nymphal development, and adult survival. Management strategies for crops in this region need to be designed to break the cycle of stink bug production, dispersal, and expansion by exploiting their edge-mediated movement and host plant preferences.

Stink bugs (Heteroptera: Pentatomidae), including Nezara viridula (L.), Euschistus servus (Say), and Chinavia hilaris (Say), are economic pests in farmscapes where they move within and between closely associated crop and non-crop habitats. Thus, field edges in these farmscapes include not only crop-to-crop interfaces but also those edges adjoining non-crop habitats. We examined the influence of field edges on colonization of stink bugs in southeastern USA farmscapes composed of typical combinations of corn, peanut, and cotton. For E. servus and N. viridula, egg-to-adult development and presence of both sexes on all crops indicated that the crops served as reproductive plants. Adult C. hilaris were rarely found on corn and on crops associated with it, and they were present mainly in cotton in peanut-cotton farmscapes. Mature crop height was significantly higher for corn than for cotton and significantly higher for cotton over peanut, and an edge effect in dispersal of stink bugs into a crop was detected up to 4.6, 8.2, and 14.6 m from the crop-to-crop interface in corn, cotton, and peanut, respectively. These results suggest that stink bug dispersal into a crop decreases as crop height increases. The first stink bug-infested crop at the crop-to-crop interface was the most significant contributor of colonizing stink bugs to an adjacent crop. An edge effect in dispersal of stink bug adults was detected in corn next to non-woodlands and woodlands and in cotton adjacent to woodlands. Edge effects were never detected in side edges of peanut. Overall, our results indicate that both plant height and host plant suitability can influence edge-mediated dispersal of stink bugs at field edges.