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Abstract Pitfall traps are frequently used to capture ground‐dwelling arthropods, particularly beetles, ants and spiders. The capture efficiency of a pitfall trapping system strongly depends on the number and opening size of traps, how traps are distributed over the sampling area (spatial arrangement) and the movement characteristics of arthropods. We use numerical simulations for a single species to analyse the trap count patterns that emerge from these variables. Arthropod movement of individuals is modelled as correlated random walks, with multiple traps placed over an area, and catches are simulated as individual interaction with traps. We consider four different types of spatial arrangements of traps across a homogeneous landscape: grid (i.e. rectangular array), transect, nested‐cross and randomised. We contextualise our results by considering the locomotion of Pterostichus melanarius, a highly active carabid beetle often serving as a biocontrol agent for the suppression of pest insects and weeds. By simulating the trapping of randomly moving ground‐dwelling arthropods, we show that there is an optimal inter‐trap separation distance (trap spacing) that maximises captures, that can be expressed using exact formulae in terms of trap opening sizes, sampling area and trap number. Moreover, for the grid and nested‐cross arrangements, larger trap spacing to maximise spatial coverage over the whole sampling area is suboptimal. Also, we find that over a large sampling area, there is a hierarchical order for spatial arrangements in relation to capture efficiency: grid, randomised, transect, followed by the nested‐cross. However, over smaller sampling areas, this order is changed as the rate at which trap counts accumulate with trap number varies across arrangements—eventually saturating at different levels. In terms of movement effects, capture efficiency is maximised over a narrow diffusive range and does not depend strongly on the type of spatial arrangement—indicating an approximate optimal mode of arthropod activity, i.e. rate of spread. Our approach simultaneously considers several important experimental design aspects of pitfall trapping providing a basis to optimise and adapt sampling protocols to other types of traps to better reflect their various purposes, such as monitoring, conservation or pest management.

Abstract Phenotypic plasticity in reproductive traits is of theoretical and applied interest as one avenue by which organisms might maintain an optimal annual reproductive routine in the face of cyclic and/or directional change in environmental conditions. We used long‐term, individual‐based data from parapatric populations of bighorn sheep (Ovis canadensis canadensis) and pronghorn (Antilocapra americana) to evaluate plasticity in breeding date, gestation duration, birth date, birth mass, and fetal growth rate in response to inter‐annual (cyclic) variation in indices of maternal energy income and expense. Traits in both species responded plastically to variation in maternal energy balance. However, despite nearly identical climate and similar vegetative habitat, plasticity was expressed in fundamentally different ways in the study species. Variation in bighorn birth date was primarily due to plasticity in breeding date, whereas variation in pronghorn birth date was primarily due to variation in gestation duration. Across traits, bighorn plastic responses were more consistent with explanations that invoked periodic energy surplus as the basis for plasticity, whereas pronghorn plastic responses were more consistent with explanations that invoked periodic energy deficiency. Later birth date was associated with increased fetal growth rate in bighorn but decreased fetal growth rate in pronghorn. Finally, we detected strong directional selection for early birth among bighorn mothers but found no evidence of selection on pronghorn birth date. Collectively, our results indicate markedly different maternal tactics for timing birth. Bighorn mothers appeared to use stored energy to subsidize the cost of birth prior to the local environmental optimum in an energy‐mediated competition with other females to minimize birth order rank. Pronghorn mothers, committed to high levels of energy allocation to offspring and subject therefore to frequent energy deficiency, timed birth conservatively to more closely match peak reproductive expenditure with peak energy income at the local environmental optimum.

Previous studies and data presented here suggest that odors from healthy host Scotch pine (Pinus sylvestris) and nonhost Norway spruce (Picea abies), as well as major monoterpenes of these trees at natural release rates, significantly reduce the attraction of flying bark beetles, Pityogenes bidentatus, of both sexes to their aggregation pheromone components grandisol and cis-verbenol in the field, as tested by slow rotation of trap pairs. In contrast, P. bidentatus males and females walking in an open-arena olfactometer in the laboratory did not avoid monoterpene vapors at release rates spanning several orders of magnitude in combination with aggregation pheromone. The bark beetle may avoid monoterpenes when flying as a mechanism for avoiding nonhost species, vigorous and thus unsuitable host trees, as well as harmful resinous areas of hosts. Inhibition of this flight avoidance response in beetles after landing would allow them to initiate, or to find and enter, gallery holes with high monoterpene vapor concentrations in order to feed and reproduce.

Studies have shown that the bark beetle Pityogenes bidentatus (Coleoptera, Curculionidae, Scolytinae) avoids volatiles of nonhost trees (Norway Spruce, birch, and oak) and healthy host Scotch Pine when orienting to aggregation pheromone. A population genetic model of two behavioral genes was hypothesized where AA, Aa, and aa were allele combinations regulating orientation to host tree and pheromone odors, and BB, Bb, and bb were combinations allowing avoidance of nonhost and unsuitable host odors. The nine possible genotypes were assigned different survival factors that remained constant during simulation. The initial proportion of aabb genotype (little aggregation/host response and little avoidance of nonhosts) was ~1.0 when a mutation was hypothesized that caused better orientation to host/beetle odors (Aabb) and another mutation causing more efficient avoidance of nonhosts (aaBb). After these initial mutations, the model used indiscriminate mating of genotypic proportions and subsequent survival as input for each successive generation. The results indicate that AABB eventually fixates in the populations in some scenarios, while AABB and other genotypes reach stable equilibriums in other models depending on genotypic survival values supported by ecologically sound assumptions. The models indicate how development of insecticide resistance in pest insects may proceed.

Competition and cooperation between bark beetles, Tomicus yunnanensis Kirkendall and Faccoli and Tomicus minor (Hartig) (Coleoptera: Scolytinae) were examined when they coexisted together in living Yunnan pine trees (Pinus yunnanensis Franchet) in Yunnan province in Southwest China. T. yunnanensis bark beetles were observed to initiate dispersal from pine shoots to trunks in November, while the majority of T. minor begins to transfer in December. T. yunnanensis mainly attacks the top and middle parts of the trunk, whereas T. minor mainly resides in the lower and middle parts of the trunk. The patterns of attack densities of these two species were similar, but with T. yunnanensis colonizing the upper section of the trunk and T. minor the lower trunk. The highest attack density of T. Yunnanensis was 297 egg galleries/m2, and the highest attack density of T. minor was 305 egg galleries/m2. Although there was significant overlap for the same bark areas, the two species generally colonize different areas of the tree, which reduces the intensity of competition for the relatively thin layer of phloem-cambium tissues where the beetles feed and reside.

The Yunnan pine shoot beetle, Tomicus yunnanensis Kirkendall and Faccoli (Coleoptera: Scolytinae) is an important pest of Yunnan pine (Pinus yunnanensis Franch) in China. Experiments with host log baits were done to develop a pest monitoring system using host tree kairomone. Five Yunnan pine logs (each 10–15 cm diam. × 30-cm long) in a trap-log bundle were treated by peeling periderm (outer bark) off to expose the phloem, and half of each log was covered with sticky adhesive to capture any attracted adult beetles. Significantly, more beetles were attracted and caught on the periderm-peeled logs (ca 30 beetles/m2 log surface/day) than on untreated control logs with adhesive (ca 2.5/m2/day). No significant differences were observed between catches on logs taken from lower or upper halves of Yunnan pines. T. yunnanensis flies mostly during the afternoon according to trap catches throughout the day. Attraction to the periderm-peeled logs decreased considerably when they were peeled further to remove the phloem, indicating phloem volatiles play a role in selection of the host by the beetle. The readily-available log baits appear useful for monitoring pine shoot beetle populations in integrated pest management programs.

A paradigm developed in the 1970s that Ips bark beetles biosynthesize their aggregation pheromone components ipsenol and ipsdienol by hydroxylating myrcene, a host tree monoterpene. Similarly, host α-pinene was hydroxylated to a third pheromone component cis-verbenol. In 1990, however, we reported that amounts of ipsenol and ipsdienol produced by male Ips paraconfusus (Coleoptera: Scolytinae) feeding in five host pine species were nearly the same, even though no detectable myrcene precursor was detected in one of these pines (Pinus sabiniana). Subsequent research showed ipsenol and ipsdienol are also biosynthesized from smaller precursors such as acetate and mevalonate, and this de novo pathway is the major one, while host tree myrcene conversion by the beetle is the minor one. We report concentrations of myrcene, α-pinene and other major monoterpenes in five pine hosts (Pinus ponderosa, P. lambertiana, P. jeffreyi, P. sabiniana, and P. contorta) of I. paraconfusus. A scheme for biosynthesis of ipsdienol and ipsenol from myrcene and possible metabolites such as ipsenone is presented. Mass spectra and quantities of ipsenone are reported and its possible role in biosynthesis of aggregation pheromone. Coevolution of bark beetles and host trees is discussed in relation to pheromone biosynthesis, host plant selection/suitability, and plant resistance.