The aphids, aphid parasitoids, and hyperparasitoids found in citrus orchards, the parasitoids' and hyperparasitoids' seasonal abundance, and the plant-aphid-parasitoid relationships in Hatay, Osmaniye, Adana, and Mersin provinces of the east Mediterranean region of Turkey are presented in the present 2-yr study. Aphidius colemani Viereck, Binodoxys angelicae (Haliday), and Lysiphlebus confusus ...

The braconid Dendrosoter protuberans and the pteromalid Cheiropachus quadrum are two parasitoids of the olive bark beetle, Phloeotribus scarabaeoides. Several chemicals such as a-pinene, b-pinene, 2-decanone, 2-nonanone, decanal, undecanal, and n-butyl acetate have been identified as attractants in the laboratory for this scolytid. Under red light at 27C in a laboratory olfactometer both parasi...

Many species of microhymenopterous parasitoids have been registered on Phyllocnistis citrella, the citrus leafminer. The present study aimed to identify the spatial distribution pattern of the native and introduced parasitoids of P. citrella in two citrus orchards in Montenegro, RS. The new shoots from 24 randomly selected trees in each orchard were inspected at the bottom (0-1.5 m) and top (1....

Interactions of the parasitoids Palmistichus elaeisis Delvare & LaSalle and Trichospilus diatraeae Cherian & Margabandhu (Hymenoptera: Eulophidae) with its alternative host Anticarsia gemmatalis (Hübner) (Lepidoptera: Noctuidae) affect the success or failure of the mass production of these parasitoids for use in integrated pest management programs. The aim of this study was to evaluate changes ...

Egg parasitoids face unique developmental constraints. First, they have exceptionally limited resources to support themselves and their siblings through three life stages. Second, they develop within the physiological system of another species, which they modify to their own ends. We examined how these constraints affect the metabolic physiology of egg parasitism, and whether parasitoids retool...

Since parasitoids can be reared from their hosts and leave evidence of parasitism after they emerge from hosts, some general outlines of their foraging behavior can be inferred from field studies that do not involve direct observation. However, direct observations are often needed to uncover critical aspects of patch use, host finding, and host use. Studies of parasitoid foraging in the field u...

The extraordinary diversity of phytophagous insects may be attributable to their narrow specialization as parasites of plants, with selective tradeoffs associated with alternate host plants driving genetic divergence of host-associated forms via ecological speciation. Most phytophagous insects in turn are attacked by parasitoid insects, which are similarly specialized and may also undergo host-...

Augmentative releases of parasitoids may be a useful tool for the area-wide management of tephritid pests. The latter are parasitized by many wasp species, though only a few of them are relevant for augmentative biocontrol purposes. To date, nearly all the actual or potential biocontrol agents for such programs are egg or larval Opiinae parasitoids (Hymenoptera: Braconidae). Here, we review the...

Genetically modified (GM) legumes expressing the α-amylase inhibitor 1 (αAI-1) from Phaseolus vulgaris L. or cysteine protease inhibitors are resistant to several bruchid pests (Coleoptera: Chrysomelidae). In addition, the combination of plant resistance factors together with hymenopteran parasitoids can substantially increase the bruchid control provided by the resistance alone. If the strateg...

We investigated the potential impact of three opiine tephritid fruit fly parasitoids: Fopius arisanus (Sonan), Fopius caudatus (Szépligeti) and Fopius ceratitivorus Wharton, on the non-target native Hawaiian tephritid, Trupanea dubautiae (Bryan), infesting flowerheads of the endemic Asteraceae shrub Dubautia raillardioides Hillebrand. The three species are the only known opiine fruit fly parasi...