Aphelinus albipodus(Hymenoptera: Aphelinidae) andDiaeretiella rapae(Hymenoptera: Braconidae) Parasitism onDiuraphis noxia(Homoptera: Aphididae) Infesting Barley Plants Differing in Plant Resistance to Aphids

Russian wheat aphid,Diuraphis noxia(Mordvilko), as a pest of small grains, has prompted research into biological control and host plant resistance. In the presence of Russian wheat aphid, leaves of a susceptible barley (Morex) are curled and chlorotic and sustain large densities of this aphid, while leaves of a resistant barley (STARS-9301B) remain flat and green and sustain fewer aphids. Might parasitism of Russian wheat aphid byAphelinus albipodusHayat & Fatima andDiaeretiella rapaeMcIntosh be affected differently by these plant types? When presented the plants separately and based on parasitism rate relative to aphid density, the largerD. rapaewas more effective in parasitizing relatively high densities of aphids within curled leaves of Morex than relatively low densities of aphids on uncurled leaves of STARS-9301B. Parasitism byA. albipodusdid not significantly differ among the plants. When given a choice of plants, approximately equal rates of parasitism occurred on the two plant lines for both parasitoid species, and parasitism byD. rapaewas greater thanA. albipodus.These data indicate that using parasitoid size as an indicator of success in a physically restricted environment may be misleading, when considered in a plant environment responsive in several manners to aphids (chlorosis, curling, and ability to sustain Russian wheat aphid). We expect that use of resistant barley will result in decreased parasitoid abundance as aphid densities decrease. However, parasitism rates are expected to be approximately equal on resistant and susceptible barley. In this system, plant resistance and biocontrol are compatible management strategies.     

Hymenopteran parasitoids and dipteran predators of the invasive aphid Diuraphis noxia after enemy introductions: Temporal variation and implication for future aphid invasions

Shifts in prevalence and abundance of hymenopteran parasitoids and dipteran predators, Diuraphis noxia, and other aphids were measured in the west-central Great Plains of North America, April–September, in 2001 and 2002, corresponding to over a decade after first detection of D. noxia and first release of D. noxia enemies. Significant temporal shifts in enemy species prevalence and diversity were detected in this study and more broadly during an 11 year time span. At any given time, some species were relatively common. One parasitoid had been predominant throughout (Aphelinus albipodus), two had shifted in dominance (Lysiphlebus testaceipes and Diaeretiella rapae), three parasitoids had been detected infrequently (Aphidius avenaphis, Aphidius matricariae, and Aphelinus asychis), one parasitoid was detected in the 1990s but not during 2001 and 2002 (Aphelinus varipes), two predatory flies occurred at occasional significant levels (Leucopis gaimarii and Eupeodes volucris), and two parasitoids may have been minor members of the fauna (Aphidius ervi and Praon yakimanum). Aphid populations detected were usually very low or not detected, precluding estimation of percent parasitism. The best evidence of suppression was observations of parasitoids in the rare case of D. noxia exceeding economic thresholds, which complemented past studies using high aphid densities. The D. noxia enemies detected were primarily endemic or long-time residents derived from previous introductions. This enemy community may provide flexibility in responding to a future aphid invasion, allowing more strategic use of biological control and other pest management approaches.     

Parasitoid spectrum (Hymenoptera: Braconidae; Aphelinidae) of the soybean aphid Aphis glycines (Homoptera: Aphididae) in Japan and Indonesia (Java and Bali)

Aphidiine and aphelinid parasitoids collected from the soybean aphid, Aphis glycines, on Glycine max in Japan and Indonesia (Java and Bali) were identified to clarify the parasitoid spectrum of the aphid there. Nine parasitoid species from Japan (Aphidiinae: Aphidius gifuensis, Aphidius sp., Binodoxys communis, Diaeretiella rapae, Lipolexis gracilis, Lysiphlebia japonica; Aphelinidae: Aphelinus asychis, A. gossypii, A. varipes) and two parasitoid species from Indonesia (B. communis, A. gossypii) were found to be associated with A. glycines.     

Hymenopteran parasitoids and dipteran predators of <Emphasis Type="Italic">Diuraphis noxia</Emphasis> in the west-central Great Plains of North America: Species records and geographic range

Parasitoids and predatory flies were sampled in the wheat production region of the west-central Great Plains (southeastern Wyoming, western Nebraska, and north-central Colorado) of North America using plant material infested with the Russian wheat aphid, Diuraphis noxia (Mordvilko) (Hemiptera: Aphididae). Samples were taken April through October in 2001 and 2002, which was 15–16 years after first detection of D. noxia and 5–6 years after the last release of natural enemies for its control in this region. The natural enemies detected were (in order of high to low detection frequencies across three states and 2 years): Aphelinus albipodus Hayat and Fatima (Hymenoptera: Aphelinidae), Eupeodes volucris Osten Sacken (Diptera: Syrphidae), Lysiphlebus testaceipes (Cresson) (Hymenoptera: Braconidae, Aphidiinae), Leucopis gaimarii Tanasijtshuk (Diptera: Chamaemyiidae), Aphidius avenaphis (Fitch), Aphidius matricariae Haliday, Diaeretiella rapae (MIntosh), Aphidius ervi Haliday, Praon yakimanum Pike and Starý (Hymenoptera: Braconidae, Aphidiinae), and Aphelinus asychis Walker (Hymenoptera: Aphelinidae). The results confirmed establishment of one of the 10 exotic parasitoid species released for D. noxia control (A. albipodus) in the west-central Great Plains. It is unknown whether detection of A. asychis, A. matricariae, and D. rapae can be attributed to exotic introductions or preexisting populations. Other species detected in this study have been previously documented from the western US, although the recognized distributions have expanded for A. avenaphis, L. gaimarii, and P. yakimanum compared to the first few years after initial detection of D. noxia. Thus, there is definitive establishment of one exotic introduced for D. noxia and considerable range expansion of preexisting species that prey upon D. noxia.     

Native primary parasitoids and hyperparasitoids attacking an invasive aphid Uroleucon nigrotuberculatum in Japan

Since the invasion of Uroleucon nigrotuberculatum from North America we searched for parasitoids of this aphid on Solidago altissima in Japan to determine what species of native parasitoids attack the newly invasive aphid. We found three primary parasitoid species: Ephedrus plagiator and Praon yomenae (Braconidae, Aphidiinae) and Aphelinus albipodus (Aphelinidae). We also found eight hyperparasitoid species: Syrphophagus sp. (Encyrtidae), Dendrocerus carpenteri (Megaspilidae), Asaphes suspensus (Pteromalidae) and Pachyneuron aphidis (Pteromalidae) through both E. plagiator and A. albipodus; Phaenoglyphis villosa (Figitidae, Charipinae), Aprostocetus sp. (Eulophidae, Tetrastichinae) and D. laticeps through E. plagiator, and Alloxysta sp. nr brevis (Figitidae, Charipinae) through A. albipodus. Uroleucon nigrotuberculatum is usually attacked by rather polyphagous primary parasitoids, E. plagiator and A. albipodus, in Japan, where an oligophagous parasitoid specialized to allied aphid species is probably absent. The hyperparasitoid community of U. nigrotuberculatum is common to those of the aphids occurring in open field‐type habitats in Japan.     

Intraguild predation on the aphid parasitoid <Emphasis Type="Italic">Aphelinus asychis</Emphasis> by the ladybird <Emphasis Type="Italic">Harmonia axyridis</Emphasis>

We investigated intraguild predation (IGP) on an aphid parasitoid, Aphelinus asychis Walker (Hymenoptera: Aphelinidae), by the multicolored Asian ladybird, Harmonia axyridis (Pallas) (Coleoptera: Coccinellidae), and used the green peach aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae) as the prey/host in the laboratory. The ladybirds reared on artificial diet and on aphids consumed more aphids than mummies, while those reared on parasitized aphids consumed similar numbers of aphids and mummies. The ladybirds chose more mummies in treatments when mummies were more abundant, and more aphids when numbers of aphids and mummies were equal, or when aphids were more abundant. However, at all density treatments, rejection rates of mummies (36%) were much greater than of aphids (2%). H. axyridis prey on more aphids than A. asychis mummies, which enhances biological control by the two species. However, prior feeding experience affected subsequent choice, increasing the competition between natural enemies which would reduce their combined effectiveness for biological control.     

An evaluation of some natural enemies of >Nezara viridula in northern California

Natural enemies associated with eggs of >Nezara viridula (L.) (Heteroptera: Pentatomidae) wereevaluated by placing sentinel egg masses inweeds and cultivated tomato and bean crops innorthern California. Egg predation wasgenerally less than 10% and normally involvedpredators with chewing mouth parts. Predatorsseldom destroyed an entire egg mass, typicallyeating <40 eggs per exploited mass.Laboratory evaluation of >25 species ofpotential arthropod predators revealed that fewfed on >N. viridula eggs to any extent;however, numerous species fed on >N.viridula nymphs. Five species of eggparasites were recovered from sentinel eggmasses: >Trissolcus basalis (Wollaston),>Gryon obesum Masner and >Telenomuspodisi Ashmead (Scelionidae); and>Ooencyrtus californicus Girault and >O.johnsoni (Howard) (Encyrtidae). The major eggparasite was >T. basalis, the only exoticmember of the parasite guild; it typicallyparasitized 100% of the eggs in an exploitedegg mass. The results indicate thatparasitization of eggs and predation of smallnymphs can be important biotic mortalityfactors for >N. viridula populations innorthern California. It is suggested that acombination of factors – viz., eggparasitization, nymphal predation, regionalshortage of overwintering sites, and localshortages of suitable hosts – maintains thisexotic pest at relatively low levels in theregion.     

Recognition of heterospecific parasitism: Competition between Aphidiid (Aphidius ervi) and Aphelinid (Aphelinus asychis) parasitoids of Aphids (Hymenoptera: Aphidiidae; Aphelinidae)

The solitary parasitoids Aphidius erviHaliday (Hymenoptera: Aphidiidae) and Aphelinus asychisWalker (Hymenoptera: Aphelinidae) attacked but generally did not oviposit in pea aphids parasitized by the other species. Wasps selectively oviposited in unparasitized hosts when given a choice. Host discrimination depended on the recognition of internal cues. Females of A. asychiseither could not recognize or ignored A. ervi'sexternal host marking pheromone. Under most conditions, A. ervisurvived in superparasitized hosts, killing competing A. asychislarvae by physical attack and possibly physiological suppression. The outcome of larval competition was not affected by oviposition sequence or age difference between larvae; A. asychissurvived only when it had substantially completed larval development before the host was superparasitized by A. ervi.It is suggested that competition for host resources incurs a cost, for the winner in terms of reduced size or increased development time and for the loser in terms of lost progeny and searching time. Consequently, heterospecific host discrimination can be functional. Internal, and probably general, cues enable wasps to recognize and avoid oviposition in hosts already parasitized by an unrelated species.     

Cold tolerance of the harlequin ladybird Harmonia axyridis in Europe

As an essential aspect of its invasive character in Europe, this study examined the cold hardiness of the harlequin ladybird Harmonia axyridis. This was done for field-collected populations in Belgium overwintering either in an unheated indoor or an outdoor hibernaculum. The supercooling point, lower lethal temperature and lower lethal time at 0 and −5 °C were determined. Possible seasonal changes were taken into account by monitoring the populations during each winter month. The supercooling point and lower lethal temperature remained relatively constant for the overwintering populations in the outdoor hibernaculum, ranging from −17.5 to −16.5 °C and −17.1 to −16.3 °C, respectively. In contrast, the supercooling point and lower lethal temperature of the population overwintering indoors clearly increased as the winter progressed, from −18.5 to −13.2 °C and −16.7 to −14.1 °C, respectively. A proportion of the individuals overwintering indoors could thus encounter problems surviving the winter due to premature activation at times when food is not available. The lower lethal time of field populations at 0 and −5 °C varied from 18 to 24 weeks and from 12 to 22 weeks, respectively. Morph type and sex had no influence on the cold hardiness of the overwintering adults. In addition, all cold tolerance parameters differed greatly between the laboratory population and field populations, implying that cold tolerance research based solely on laboratory populations may not be representative of field situations. We conclude from this study that the strong cold hardiness of H. axyridis in Europe may enable the species to establish in large parts of the continent.     

Reproductive compatibility and genetic variation between two strains of Aphelinus albipodus (Hymenoptera: Aphelinidae), a parasitoid of the soybean aphid, Aphis glycines (Homoptera: Aphididae)

Aphelinus albipodus Hayat and Fatima is a potential biological control agent of the soybean aphid, Aphis glycines Matsumura, which is a newly introduced soybean pest in the United States. We compared the reproductive compatibility and molecular genetic variation between two geographic strains of A. albipodus. One strain was collected from soybean aphids in Japan and the other recovered from Russian wheat aphid, Diuraphis noxia (Mordvilko), in the western U.S., populations of which were established with parasitoids imported from Eurasia. We present results of crossing experiments between the two strains, genetic differences based on RAPD-PCR markers, rDNA ITS1 and ITS2 gene sequences, and presence of Wolbachia in the two strains using PCR amplification of the wsp gene. We found no reduction in the production of females in reciprocal crosses between strains, but a significant reduction in fecundity when F₁ females stemming from one of the reciprocal crosses were backcrossed to males from either source. The two strains differed by 3.4% in the rDNA ITS1 sequence and by presence/absence of one RAPD-PCR marker from a total of 20 RAPD primers screened, but their rDNA ITS2 sequences were identical. We used restriction enzyme analysis to separate the strains by differential digestion of the ITS1 PCR product. Wolbachia was present in 100% of males and females of both strains of A. albipodus.     

Instar-specific defense of the pea aphid,Acyrthosiphon pisum: Influence on oviposition success of the parasiteAphelinus asychis (Hymenoptera: Aphelmidae)

The parasite Aphelinus asychisWalker (Hymenoptera: Aphelinidae) oviposits in all four instars of the pea aphid, Acyrthosiphon pisum(Harris) (Homoptera: Aphididae). Searching females display a highly stereotyped sequence of behaviors when encountering a host. Once recognized, an aphid is examined and probed by the wasp with the everted ovipositor prior to oviposition. Oviposition success is influenced by aphid behavior that is related to aphid size and expressed through instarspecific escape and defense reactions. Being smaller and less able to defend themselves, first and early-second instars of pea aphid are more susceptible to successful parasitism than third and fourth instars, in that order. Observed patterns of preference by Aphelinus females for particular aphid species and instars reflect the outcome of behavioral interactions between the hosts and the parasites, rather than preference in the strict sense.     

Release and recovery in South Africa of the exotic aphid parasitoid <Emphasis Type="Italic">Aphelinus hordei</Emphasis> verified by the polymerase chain reaction

The exotic aphid parasitoid Aphelinushordei Kurdjumov (Hymenoptera: Aphelinidae) was released at five Russian wheat aphid [Diuraphis noxia (Mordvilko)] infested wheat fields in the eastern parts of the Free State Province of South Africa during the 1998 and 1999 growing seasons. Except for differences in the setae on the ventralside of the forewings, this species is verysimilar in colour and structure to A.varipes (Foerster) and A. albipodusHayat & Fatima, which also parasitise D.noxia. It is therefore difficult todistinguish between them, and to determinetheir establishment. Therefore a polymerasechain reaction, using specific primers for bothITS2 and mitochondrial 16s DNA sequencesof the three parasitoids, followed by HinfIrestriction endonuclease digestion and agarosegel electrophoresis, was tested to distinguishbetween them. Parasitoid recoveries were madeat the release sites within weeks after theywere released. Putative individuals of A.hordei were also collected during 1999 and2000 on D. noxia in Lesotho, whichis situated on the eastern border of the FreeState Province. The procedure separated the three Aphelinus spp.reliably. Between 94 and 100% of theindividuals recovered during the two fieldseasons were identified as being A.hordei, thus verifying recovery of this exoticaphid parasitoid in South Africa.     

Interactions betweenAcyrthosiphon kondoi [Homoptera: Aphidoidea] andAphelinus asychis [Hymenoptera: Chalcidoidea] and other parasites and hosts

In laboratory trials to investigate the parasite/host spectra of certain aphid pests and hymenopterous parasites, the aphidAcyrthosiphon kondoi Shinji encapsulated the egg of the aphelinid parasiteAphelinus asychis Walker. The resultant brown, sclerotic capsule was formed within 24 h of exposure of the aphid to parasitization and as far as is known prevented the development of the parasite to the larval stage. The capsule remained throughout the life of the aphid, whose longevity and fecundity were apparently not seriously impaired. A small number ofAphelinus escaped encapsulation, especially in aphids already containing capsule(s), and developed into normal, reproductive adults.A. kondoi did not encapsulate, andA. asychis was not encapsulated by any other species. However, thoughA. asychis readily parasitizedAphis citricola van der Goot,A. nerii Boyer de Fonscolombe andToxoptera citricidus (Kirkaldy), most of its progeny ceased development in these aphids before reaching the mummification stage, and died within the dead or dying, non-mummified aphid host.     

The temperature-dependent duration of development and parasitism of three cereal aphid parasitoids, Aphidius ervi, A. rhopalosiphi, and Praon volucre

Temperature dependencies were established for the egg-to-mummy and mummy-to-adult phases, for mummy mortality, and for parasitism of Aphidius ervi Haliday, Aphidius rhopalosiphi De Stefani-Perez, and Praon volucre (Haliday) (Hymenoptera, Aphidiidae), three parasitoids of Sitobion avenae (Fabricius) (Homoptera, Aphididae), at 8°C, 12°C, 16°C, 20°C, and 25°C on winter wheat (cv. Haven). A physiological model described temperature-dependent development over the full temperature range, whereas a linear model was fitted for data above 8°C and used to estimate the lower temperature thresholds and day-degrees (° D) required for development. The thresholds for A. ervi were 2.2°C for egg-mummy development and 6.6°C for mummy-adult development, those for A. rhopalosiphi were 4.5°C and 7.2°C, and those for P. volucre were 3.8°C and 5.5°C. The time to develop into mummies and adults differed significantly between the three species: A. ervi development into mummies required an average of 159 ° D, while development into adults took an average of 73 ° D. The corresponding average times required for A. rhopalosiphi and P. volucre to develop mummies were 124° D and 126° D, while their development into adults required an average of 70° D and 150° D, respectively. Mummy mortality was 25–35% at 8°C and less at the higher temperatures tested, but began to increase again at 25°C, showing a quadratic relationship between mortality and temperature. Parasitization was very low or, in the case of P. volucre, absent up to 12°C and thereafter increased with increasing temperature. The relationship between parasitization, recorded as percent aphids mummified, and temperature was linear at the temperatures tested and depended on species. A. ervisuperparasitized 11.1% aphids at 20°C and 16.6% aphids at 25°C, whereas superparasitism was low in A. rhopalosiphi and absent in P. volucre. From 16°C to 25°C the P. volucre sex ratio increased. For A. ervi and A. rhopalosiphi there was no trend with temperature, but at 20°C and 25°C it was close to even. Field data for 1996 and 1997 allowed for a comparison of actual and expected emergence of overwintering mummies. In both years, parasitoids were predicted to have emerged from overwintering mummies well in advance of the onset of aphid infestation, and more than a month earlier than the first parasitized aphids were found in winter wheat. Observations from trap plants in other crops supported the predictions of the models. Other factors that can affect biological control by cereal aphid parasitoids are discussed.     

Functional responses of aphid parasitoids,Aphidius colemani (Hymenoptera: Braconidae) and Aphelinus asychis (Hymenoptera: Aphelinidae)

We evaluated the functional responses of two aphid parasitoids: Aphidius colemani on the green peach aphid Myzus persicae (Hemiptera: Aphididae), and Aphelinus asychis on M. persicae and the potato aphid, Macrosiphum euphorbiae (Hemiptera: Aphididae). Parasitoid oviposition occurred at host densities of 5, 10, 20, 30, 50, 80 or 100 aphids for A. colemani and 5, 10, 20, 30 or 50 aphids for A. asychis. More M. persicae were parasitized by A. colemani than by A. asychis at an aphid density of 50. Among the three types of functional response, type III best described the parasitoid response to the host densities both in A. colemani and A. asychis. The estimated handling time was shorter for A. colemani than for A. asychis (0.017 and 0.043 d, respectively). The proportion of aphids that were parasitized exhibited the same characteristic curve among the three host-parasitoid combinations: a wave form that appeared to be a composite of a decelerating (as in type II) response at low host density and an accelerating-and-decelerating (as in type III) response at medium to high host density. We hypothesize that the novel host species (and its host plant), density-dependent superparasitism, and/or density-dependent host-killing may have induced the modified type III response.     

Diapause termination and thermal requirements for postdiapause development inAphelinus mali at constant and fluctuating temperatures

Diapause termination under natural and simulated overwintering conditions, the effect of subzero temperature on postdiapause development and the relationship between postdiapause development rate and constant and fluctuating temperatures was studied in a Dutch population ofAphelinus mali Hald. (Hymenoptera: Aphelinidae).The rate of diapause termination was similar in larvae overwintering under natural and simulated conditions. Most larvae had terminated diapause by the last week of February. Some female larvae may have remained in diapause until the end of March. The exposure of postdiapause larvae to –10°C for two weeks did not affect their survival or postdiapause development rate.PostdiapauseA. mali larvae could complete development and the adults emerge from their mummified aphid hosts at constant temperatures from 12 to 24°C. Although some larvae completed postdiapause development at 10°C, few emerged. The theoretical threshold temperature (t_o) for postdiapause development was 9.4°C and the thermal constant (K) 136.4 degree-days. K was 121.4 and 134.8 for first and 50% emergence, respectively.The number of heat units accumulating above 9.4°C to 1st and 50% emergence was similar under constant and fluctuating temperatures.

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Fin de la diapause et exigences thermiques pour le développement après la diapause d'Aphelinus mali soumis à des températures constantes ou à des thermopériodes

Résumé L'achèvement de la diapause en conditions naturelles ou simulant l'hiver, les effets des températures inférieures à zéro sur le développement après la diapause et les relations entre la vitesse de développement après la diapause et les températures constantes ou en thermopériodes ont été examinés sur des populations néerlandaises d'A. mali (Hymenop.; Aphélinidae).Les taux d'achèvement de la diapause de larves hivernantes étaient semblables en conditions naturelles ou simulées. La plupart des larves ont terminé leur diapause la dernière semaine de février. Quelques larves femelles sont restées en diapause jusqu'à fin mars. L'exposition pendant 2 semaines des larves sorties de diapause à –10 °C ne compromet pas leur survie ou leur taux de développement après la diapause.Les larves ayant diapause peuvent terminer leur développement et les adultes émerger des pucerons momifiés aux températures constantes comprises entre 12 et 24 °C. Bien que quelques larves achèvent leur développement à 10 °C, peu émergent. La température seuil théorique de développement après la diapause (t_o) a été de 9,4 °C et la constante thermique (K), 136,5 degrés-jours. Pour la première émergence et pour 50% d'émergences, les valeurs de K étaient respectivement: 121,4 et 134,8.Le nombre d'unités thermiques pour la première émergence et pour 50% d'émergences était le même à température constante ou avec une thermopériode.

     

Interspecific host discrimination and intrinsic competition between Aphelinus asychis and Aphidius gifuensis in Myzus persicae

Aphelinus asychis Walker (Hymenoptera: Aphelinidae) and Aphidius gifuensis Ashmead (Hymenoptera: Braconidae: Aphidiinae) are solitary kionobiont endoparasitoids, which can parasitize the green peach aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae). We determined the influence of oviposition sequence and various time intervals (0, 24, 48, and 72 h) between two ovipositions on self‐ and conspecific discrimination and interspecific intrinsic competition between A. asychis and A. gifuensis. When offered unparasitized M. persicae and those parasitized by the other parasitoid species, the two parasitoid species oviposited more often in unparasitized hosts. Aphelinus asychis and A. gifuensis could, however, not avoid to multiparasitize hosts parasitized by the other species. Both parasitoid species had a limited interspecific discrimination ability through ovipositor insertion to detect internal cues. Aphidius gifuensis most often out‐competed A. asychis. The outcome of this interspecific competition was not influenced by oviposition sequence or time intervals between two ovipositions. Aphidius gifuensis eliminated competitors by physical combat at the first instar and probably by physiological suppression in later stages; A. asychis possibly used physiological suppression in all larval stages.     

Parasitoids acquired byColeophora parthenica [Lepidoptera: Coleophoridae] ten years after its introduction into southern California for the biological control of Russian thistle

Parasitism of the stem and branch-boring mothColeophora parthenica Meyrick [Lepidoptera: Coleophoridae], introduced into California for the biological control of Russian thistle,Salsola australis R. Brown [Chenopodiaceae] was studied in the Coachella Valley of southern California during 1985–1986. Eight parasitoid species were reared from overwintering larvae ofC. parthenica, but none from the F₁ larvae, and just 2 individuals of one species from the F₂ summer generation. The level of parasitism of overwintering larvae was positively correlated with branch diameter, and ranged from 2% in the primary (main) branches to 45% in the tertiary branches in the spring 1985 sample, and from 2% to 19% in the spring 1986 sample, respectively. Rates of parasitism>20% were only found at sites with higher plant cover and chenopod diversity, but no other plant source or alternate hosts of the parasitoids ofC. parthenica were found. The 2 dominant species, the solitary, hymenopterous ectoparasitoids,Norbanus perplexus (Ashmead) [Pteromalidae] andEurytoma strigosa Bugbee [Eurytomidae], are both congeners of native parasitoids ofC. parthenica in Pakistan. The 2 other species of parasitoids ofC. parthenica in southern California for which other hosts are known are polyphagous and external on the larvae. No specialized endoparasitoid Braconidae, like those which dominate the native parasitoid complex in Pakistan and the U.S.S.R., have transferred toC. parthenica during its first 10 years in southern California.      

Distribution, host specificity, and overwintering of Celatoria bosqi Blanchard (Diptera: Tachinidae), a South American parasitoid of Diabrotica spp. (Coleoptera: Chrysomelidae: Galerucinae)

The genus Diabrotica (Coleoptera: Chrysomelidae) includes a great number of pest species, including some of the most important crops pests of the Americas. However, only five parasitoid species have been recorded for it. The parasitoid Celatoria bosqi Blanchard was the first parasitoid described from Diabrotica spp. in South America, where substantial parasitism has been observed. C. bosqi has been collected almost throughout the South American distribution of its main host, Diabrotica speciosa (Germar), in an area that includes temperate and tropical lowlands, and semiarid to humid highlands. Three Diabrotica species were found to host the parasitoid, D. speciosa (Germar), Hystiopsis sp., and Diabrotica viridula (F.), with a total parasitism of 2.60, 5.55, and <0.02%, respectively. Laboratory experiments with field beetles and puparia, reared in the laboratory, indicate that C. bosqi overwinters obligatorily in overwintering adult host beetles, remaining quiescent in its live host below developmental temperatures. Based on the known climatic range of C. bosqi, and its requirement of adult overwintering hosts, a potential distribution in North America is projected.     

Effect of parasitism on flight behavior of the soybean aphid, Aphis glycines

Many aphid species possess wingless (apterous) and winged (alate) stages, both of which can harbor parasitoids at various developmental stages. Alates can either be parasitized directly or can bear parasitoids eggs or larvae resulting from prior parasitism of alatoid nymphs. Winged aphids bearing parasitoid eggs or young larvae eventually still engage in long-distance flights, thereby facilitating parasitoid dispersal. This may have a number of important implications for biological control of aphids by parasitoids. In this study, we determined the effect of parasitism by Aphelinus varipes (Hymenoptera: Aphelinidae) on wing development and flight of the soybean aphid, Aphis glycines (Hemiptera: Aphididae). We also quantified the influence of aphid flight distance on subsequent A. varipes development. Parasitism by A. varipes was allowed at different A. glycines developmental stages (i.e., alatoid 3rd and 4th-instar nymphs, alates) and subsequent aphid flight was measured using a computer-monitored flight mill. Only 35% of aphids parasitized as L3 alatoid nymphs produced normal winged adults compared to 100% of L4 alatoids. Flight performance of aphids parasitized as 4th-instar alatoid nymphs 24 or 48 h prior to testing was similar to that of un-parasitized alates of identical age, but declined sharply for alates that had been parasitized as 4th-instar alatoid nymphs 72 and 96 h prior to testing. Flight performance of aphids parasitized as alate adults for 24 h was not significantly different from un-parasitized alates of comparable ages. Flight distance did not affect parasitoid larval or pupal development times, or the percent mummification of parasitized aphids. Our results have implications for natural biological control of A. glycines in Asia and classical biological control of the soybean aphid in North America.