Plants respond to herbivory with the emission of induced plant volatiles. These volatiles may attract parasitic wasps (parasitoids) that attack the herbivores. Although in this sense the emission of volatiles has been hypothesized to be beneficial to the plant, it is still debated whether this is also the case under natural conditions because other organisms such as herbivores also respond to t...

This study investigated the interactions of the pupal fruit ßy parasitoid, Dirhinus giffardii Silvestri, with each of four eggor larval-pupal fruit ßy parasitoids: Fopius arisanus (Sonan), Diachasmimorpha longicaudata (Ashmead), Diachasmimorpha kraussii Fullaway, and Psyttalia concolor (Szépligeti) in Hawaii. F. arisanus attacks host eggs, whereas the other three attack host larvae; all four pa...

Agricultural landscapes can be characterized as a mosaic of habitat patches interspersed with hostile matrix, or as a gradient of patches ranging from suitable to unsuitable for different species. Arthropods moving through these landscapes encounter a range of edges, with different permeability. Patches of native vegetation in these landscapes may support natural enemies of crop pests by provid...

Emerald ash borer (EAB), Agrilus planipennis Fairmaire, native to Asia, is killing ash trees (Fraxinus spp.) across 15 states and southeastern Canada. Integrated pest management using biological control is the only viable long-term approach for controlling the spread of EAB outside of host resistance. Three hymenopteran parasitoids, Spathius agrili Yang, Tetrastichus planipennisi Yang, and Oobi...

The eastern cherry fruit fly, Rhagoletis cingulata Loew (Diptera: Tephritidae), is an economically important pest of cherries in North America. In 1983 it was first reported in Europe where it shares its ecological niche with the native European cherry fruit fly, Rhagoletis cerasi L. (Diptera: Tephritidae). Their coexistence in Europe led to the recent horizontal transmission of the Wolbachia s...

Mortality during the immature development of T. galloi and T. pretiosum was estimated on UV-killed and live eggs of a factitious and a natural host, respectively. A staining technique was used to determine the actual parasitization of UV-treated eggs and was compared with the number of parasitoids that emerged per host egg (detectable parasitization). Effects of temperature as a factor of morta...

Plants are exposed to a suite of herbivorous attackers that often arrive sequentially. Herbivory affects interactions between the host plants and subsequently attacking herbivores. Moreover, plants may respond to herbivory by emitting volatile organic compounds (VOCs) that attract carnivorous natural enemies of the herbivores. However, information borne by VOCs is ubiquitous and may attract car...

The synthetic juvenile hormone analogue (S)-hydroprene can control populations of the oriental cockroach Blatta orientalis Linnaeus. Eradication of B. orientalis infestations, however, can take in excess of two years. In an attempt to reduce the time (S)-hydroprene takes to eliminate a population of oriental cockroaches, we explored the possibility of using the oothecal endoparasitoid Aprostoce...

Models of host-parasite coevolution predict pronounced genetic dynamics if resistance and infectivity are genotype-specific or associated with costs, and if selection is fueled by sufficient genetic variation. We addressed these assumptions in the black bean aphid, Aphis fabae, and its parasitoid Lysiphlebus fabarum. Parasitoid genotypes differed in infectivity and host clones exhibited huge va...

Climate and land use change can alter the incidence strength of biotic interactions, with important effects on distribution, abundance function species. To assess importance these their dynamics, studies quantifying how interactions in space time are needed. We studied between nettle-feeding butterflies shared natural enemies (parasitoids) locally across 500 km latitudinal gradient Sweden. also...