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.     

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.     

Untangling the aphid-parasitoid food web in citrus: Can hyperparasitoids disrupt biological control?

Molecular techniques are irreplaceable to untangle the trophic links in communities where immature entomophagous species (either in the third or fourth level) develop inside the phytophagous. This is the case of aphid-parasitoid communities. Here, we develop a DNA-based approach to untangle the structure of the aphid-parasitoid food web in citrus, where Aphis spiraecola Patch. (Hemiptera: Aphididae) is a key pest and Binodoxys angelicae Haliday (Hymenoptera: Braconidae), its dominant primary parasitoid, is attacked by a complex of hyperparasitoids. Aphid populations and parasitism were followed at weekly intervals in 2012 and 2013. Parasitism rates were low (∼0.04 in the four sampled orchards). Simultaneously, colonies harboring aphid mummies were collected. Approximately half of the mummies were reared to adulthood and at least six hymenopteran hyperparasitoid species were identified by classical means: Syrphophagus aphidivorus (Mayr) (Encyrtidae), Alloxysta sp. (Forster) (Figitidae), Asaphes sp. (Walker) (Pteromalidae), Pachyneuron aphidis (Bouché) (Pteromalidae), Dendrocerus sp. (Ratzeburg) (Megaspilidae) and Phaenoglyphis villosa (Hartig) (Figitidae). The other half was subjected to a Taqman-based multiplex PCR to investigate trophic relationships in this food web. We confirmed that all six species hyperparasitized B. angelicae. The most abundant hyperparasitoids were S. aphidivorus and Alloxysta sp. Both were abundant from the beginning of the season, and hyperparasitism rates remained high (∼0.4) throughout the season in the two study years. Although these species could share the same mummy, S. aphidivorus and Alloxysta sp. were the most abundant species and dominated this food web. Finally, hyperparasitoids also increased the secondary sex ratio of B. angelicae. Thus, hyperparasitism probably explains the low impact of B. angelicae on A. spiraecola populations.     

Hyperparasitoids of the gum leaf skeletoniser, Uraba lugens Walker (Lepidoptera: Nolidae), with implications for the selection of a biological control agent for Uraba lugens in New Zealand

Abstract  The hyperparasitoids reared from three species of primary parasitoids of the gum leaf skeletoniser, Uraba lugens Walker (Lepidoptera: Nolidae) collected in South Australia and Tasmania are recorded and discussed. Seven hyperparasitoids were reared. Diatora sp. and ? Paraphylax sp. (Ichneumonidae: Cryptinae); Tetrastichus sp. (Chalcidoidea: Eulophidae); Megadicylus dubius (Girault) (Chalcidoidea: Pteromalidae) and Elasmus sp. (Chalcidoidea: Eulophidae) were reared from Cotesia urabae Austin and Allen (Braconidae: Microgastrinae). Megadicylus dubius , Elasmus sp. and Anastatus sp. (Chalcidoidea: Eupelmidae) were reared from Dolichogenidea eucalypti Austin and Allen (Braconidae: Microgastrinae). Pediobius bruchicida (Rondani) (Chalcidoidea: Eulophidae) was reared from Euplectrus sp. (Chalcidoidea: Eulophidae). This appears to be the first record of the cryptine ichneumonid genus Diatora Förster from Australia. Of the seven hyperparasitoid species reared, only one ( P. bruchicida ) is known to be present in New Zealand. Implications for the selection of a biological control agent for U. lugens in New Zealand are discussed. Some prior misidentifications of associated hyperparasitoids are noted.     

Cardinium in Plagiomerus diaspidis (Hymenoptera: Encyrtidae)

The bacterial symbiont Cardinium (Bacteroidetes) was previously implicated in the thelytokous reproduction of the parasitoid Plagiomerus diaspidis Crawford (Hymenoptera: Encyrtidae). Horizontal transmission of the symbiont among the cactus scale Diaspis echinocacti Bouché (Homoptera: Diaspididae) and its hymenopteran parasitoids has been suggested. In this study, the bacteria associated with D. echinocacti, its parasitoids P. diaspidis and Aphytis sp. (Hymenoptera: Aphelinidae), and the hyperparasitoid Marietta leopardina Motschulsky (Hymenoptera: Aphelinidae) were characterized using molecular fingerprinting techniques, and the localization of Cardinium in P. diaspidis was studied using fluorescence in situ hybridizations (FISH). Cardinium was the only bacterium found in P. diaspidis, but it could not be detected in any of the other insects tested. The symbiont was specifically located in the reproductive tissues of its P. diaspidis host.     

Non-target parasitism of the endemic New Zealand red admiral butterfly (Bassaris gonerilla) by the introduced biological control agent Pteromalus puparum

The New Zealand red admiral butterfly, Bassaris gonerilla (F.) (Lepidoptera: Nymphalidae), has been known as a non-target host for the introduced biological control agent Pteromalus puparum (L.) (Hymenoptera: Pteromalidae) for at least 35 years, but the level of parasitism has never been quantified. Pre-imaginal mortality in B. gonerilla was assessed over the southern summer of 2000/01 at six field sites in the Christchurch area of the South Island, New Zealand. Individual eggs and larvae were identified by tagging the stem of the Urtica ferox Forst.f. plant on which they were found and the fate of these individuals was checked weekly. These data were used to construct a partial life table for B. gonerilla. Egg mortality was very high (95%), with parasitism by an unidentified Telenomus sp. Haliday (Hymenoptera: Scelionidae) causing 57% mortality. Mortality in the larval and pupal stages increased at a constant rate with age and the major mortality factor was disappearance, which was assumed to be a result of predation and dispersal of larvae. The introduced biological control agent P. puparum parasitized 14% of B. gonerilla pupae sampled. However, parasitism by another exotic parasitoid, the self-introduced Echthromorpha intricatoria (F.) (Hymenoptera: Ichneumonidae), was even higher at 26%. A survey of pupal parasitism in three regions of New Zealand (Wellington, Christchurch, and Dunedin) revealed overall parasitism levels of 67% by E. intricatoria and 8% by P. puparum, but due to the difference in emergence times of B. gonerilla and its parasitoids, these are likely to be overestimates of percent parasitism. It is concluded that P. puparum has permanently enhanced mortality in B. gonerilla, but the level of mortality is low relative to egg parasitism by Telenomus sp., larval disappearance mortality, and pupal mortality due to E. intricatoria parasitism. To determine if this level of pupal parasitism has had population effects will require more data and the development of a population model for B. gonerilla.     

Occurrence and activity of <Emphasis Type="Italic">Bemisia tabaci</Emphasis> parasitoids on cassava in different agro-ecologies in Uganda

Bemisia tabaci Gennadius (Homoptera: Aleyrodidae) is the vector of cassava mosaic geminiviruses that cause cassava mosaic disease (CMD), which in turn causes devastating yield losses. Surveys were conducted from October 2000 to November 2001 in four agro-ecologies in Uganda to enhance the understanding of parasitoid fauna and parasitism of B. tabaci in cassava fields. Such an understanding is an essential prerequisite for the development of biological control methods of B. tabaci to complement current CMD control practices. Parasitoid abundance and parasitism efficiency varied between locations and sampling dates within the locations; highest parasitoid densities were observed at Namulonge in the Lake Victoria crescent while the lowest was at Kalangala. In all locations, parasitism was mainly due to Encarsia sophia Dodd and Girault and Eretmocerus mundus Mercet (all Hymenoptera: Aphelinidae). Two occasionally observed species included Encarsia mineoi Viggiani (Hymenoptera: Aphelinidae), only observed at Namulonge, and blackhead Encarsia (Hymenoptera: Aphelinidae) observed at Bulisa, Namulonge and Lyantonde. Parasitism efficiency was highest at Bulisa (57.9%), but ranged from 40.2 to 46.9% at the other three sites. This paper discusses the possible causes of variations in parasitoid abundance and parasitism efficiency, and proposes further studies that might be carried out to assess the potential for augmentation of parasitoids to control B. tabacipopulations and CMD.     

Host selection by the heteronomous hyperparasitoid Encarsia pergandiella: multiple-choice tests using Bemisia argentifolii as primary host

The ovipositional patterns of the heteronomous hyperparasitoid Encarsia pergandiella Howard (Hymenoptera: Aphelinidae) in the presence of its primary host Bemisia argentifolii Bellows & Perring (Hemiptera: Aleyrodidae), and in the presence or absence of conspecific and heterospecific secondary hosts (Encarsia formosa Gahan andEretmocerus mundus Mercet; Hymenoptera: Aphelinidae) were examined to assess host species preferences. Host preferences by heteronomous hyperparasitoids may affect the relative abundance of co-occurring parasitoid species and may influence host population suppression by the parasitoid community. Four combinations of hosts were tested: (1) B. argentifolii, E. mundus, and E. formosa, (2) B. argentifolii, E. formosa, and E. pergandiella, (3) B. argentifolii, E. mundus, and E. pergandiella, and, (4) B. argentifolii, E. mundus, E. formosa, and E. pergandiella. Arrays of hosts (24) were constructed in Petri dishes using leaf disks, each bearing one host. Thirty arrays of each host combination were exposed to single females for 6 h. All hosts were dissected to determine number of eggs per host. Encarsia pergandiella parasitized E. formosa hosts as frequently as E. mundus hosts. However, E. pergandiella parasitized either of these heterospecific hosts more frequently than conspecific hosts in treatments including two secondary host species. When a third parasitoid species was included in host arrays, E. pergandiella parasitized conspecific hosts as frequently as heterospecific hosts. Developmental stage of the hosts did not significantly influence host species selection by E. pergandiella. Our results indicate that host selection and oviposition by heteronomous hyperparasitoids like E. pergandiella, vary with the composition of hosts available for parasitization, and suggest a preference for heterospecific over conspecific secondary hosts.     

Costs of secondary parasitism in the facultative hyperparasitoid Pachycrepoideus dubius: does host size matter?

Although hyperparasitism frequently occur in parasitic insects, many aspects of this strategy remain unknown. We investigated possible fitness costs of hyperparasitism as influenced by host size. Our study was conducted with the facultative hyperparasitoid Pachycrepoideus dubius Ashmead (Hymenoptera: Pteromalidae), which parasitizes host species differing greatly in size. We compared some fitness traits (level of successful parasitism, development time, sex ratio and offspring size) of P. dubius developing on large secondary/primary (Delia radicum L. (Diptera: Anthomyiidae)/Trybliographa rapae Westwood (Hymenoptera: Figitidae)) or small secondary/primary host species (Drosophila melanogaster L./Asobara tabida Nees (Hymenoptera: Braconidae)). In no-choice and choice experiments, P. dubius was able to develop on different stages of T. rapae (L2 (endophagous), L4 (ectophagous), and pupae) but that it preferred to parasitize unparasitized D. radicum pupae over pupae parasitized by T. rapae. Furthermore, in P. dubius, hyperparasitism was associated with fitness costs (lower level of successful parasitism, smaller adult size) and these costs were greater on the smallest host complex. We hypothesize that the size of D. melanogaster pupae parasitized by A. tabida may be close to the suboptimal host size for P. dubius beneath which the costs of hyperparasitism make this strategy nonadaptive. Hyperparasitism in terms of trade-offs between host quality and abundance of competitors is discussed.     

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.     

Host-feeding and egg maturation byPachycrepoideus vindemiae

Pachycrepoideus vindemiae Rondani (Hymenoptera: Pteromalidae) is a facultative hyperparasitoid ofDrosophila parasitoids in Europe. FemaleP. vindemiae host-feed from the same hosts into which they lay eggs and this enables them to mature additional eggs.P. vindemiae females were allowed to host-feed from puparia containingDrosophila melanogaster Meigen (Diptera: Drosophilidae) pupae or pupae ofAsobara tabida Nees (Hymenoptera: Braconidae). Wasps which had host-fed carried significantly more eggs; the species of host which was fed from had no significant effect on the number of mature eggs in the ovaries. Host-feeding caused no significant reduction in the size of the emerging offspring.P. vindemiae were allowed to forage over patches containing different frequencies of the two host species. No significant oviposition preference was found but there were marked host-feeding preferences which were affected by the age of the host pupae. It is suggested that these preferences were due to the physical nature of the hosts which were fed from.     

Foraging behaviour at the fourth trophic level: a comparative study of host location in aphid hyperparasitoids

In studies of foraging behaviour in a multitrophic context, the fourth trophic level has generally been ignored. We used four aphid hyperparasitoid species: Dendrocerus carpenteri (Curtis) (Hymenoptera: Megaspilidae), Asaphes suspensus Walker (Hymenoptera: Pteromalidae), Alloxysta victrix (Westwood) (Hymenoptera: Alloxystidae) and Syrphophagus aphidivorus (Mayr) (Hymenoptera: Encyrtidae), to correlate their response to different cues with their ecological attributes such as host range and host stage. In addition, we compared our results with studies of primary parasitoids on the same plant–herbivore system. First, the olfactory response of females was tested in a Y‐tube olfactometer (single choice: plant, aphid, honeydew, parasitised aphid, aphid mummy, or virgin female parasitoid; dual choice: clean plant, plant with aphids, or plant–host complex). Second, their foraging behaviour was described on plants with different stimuli (honeydew, aphids, parasitised aphids, and aphid mummies). The results indicated that olfactory cues are probably not essential cues for hyperparasitoid females. In foraging behaviour on the plant, all species prolonged their total visit time and search time as compared to the control treatment (clean plant). Only A. victrix did not react to the honeydew. Oviposition in mummies prolonged the total visit time because of the long handling time, but the effect of this behaviour on search time could not be determined. No clear correlation between foraging behaviour and host stage or host range was found. In contrast to specialised primary aphid parasitoids that have strong fixed responses to specific kairomones and herbivore‐induced synomones, more generalist aphid hyperparasitoids seem to depend less on volatile olfactory stimuli, but show similarities with primary parasitoids in their use of contact cues while searching on a plant.     

Survey for parasites ofSesamia calamistis (Lep.: Noctuidae) andEldana saccharina (Lep.: Pyralidae) in southwestern Nigeria

Field surveys were conducted during 1990–92 to document the relative abundance of different species of parasites of the lepidopterous stem borersSesamia calamistis Hampson andEldana saccharina Walker in maize fields in southwestern Nigeria. Species of parasitoids detected on both stem borers included the larvalpupal parasitoidsSturmiopsis parasitica Curran (Diptera: Tachinidae) andBrachymeria feae Masi (Hymenoptera: Chalcididae), and the larval parasitoidDolichogenidea polaszeki Walker (Hymenoptera: Braconidae). The braconidCotesia sesamiae (Cameron) was found attackingS. calamistis. The hyperparasitoidExoristobia dipterae (Risbec) (Hymenoptera: Encyrtidae) was detected on a pupa ofS. parasitica. Parasitic nematodes belonging toMermis sp. and/orHexamermis sp. were found infesting larvae of both stem borers. Overall, larval/pupal parasitization levels at Ibadan were low and ranged from 4.2 to 22.8% forS. calamistis and 1.2 to 13% forE. saccharina. Of the parasites found,S. parasitica was the most common, followed by nematodes. Four hymenopteran egg parasitoids were found attackingS. calamistis: Telenomus busseolae Gahan,T. isis Polaszek (Scelionidae),Lathromeris ovicida Risbec, andTrichogrammatoidea eldanae Viggiani (Trichogrammatidae). Egg parasitization ranged from 13.4 to 41.5%. The only egg parasitoid detected onE. saccharina wasTelenomus applanatus Bin and Johnson, which inflicted only 5% parasitization.     

Hyperparasitoid aggregation in response to variation in Aphidius ervi host density at three spatial scales

1. This article investigates the pattern of hyperparasitism of the host Aphidius ervi Haliday (Hymenoptera, Aphidiidae), a primary parasitoid of the pea aphid, Acyrthosiphon pisum (Harris) (Homoptera: Aphididae) at three spatial scales.
2. In the laboratory, the hyperparasitoid Asaphes lucens (Provancher) (Hymenoptera: Pteromalidae) was introduced into cages containing sixteen alfalfa plants with varying numbers of A. ervi mummies (the stage susceptible to hyperparasitism). The pattern of hyperparasitism at the end of the 48-h trials showed no density-dependent hyperparasitoid aggregation, although there was strong density-independent hyperparasitoid aggregation.
3. In the field, the density of A. ervi mummies was manipulated in twelve 2 × 2-m plots containing 1309–1654 alfalfa stems. Variation in hyperparasitism among plots showed no density-dependent aggregation, although there was strong density-independent aggregation.
4. Finally, at the largest scale of the study, the distribution of hyperparasitism was sampled among twelve alfalfa fields within a 5 × 3-km area. At this scale there was both density-dependent and density-independent hyperparasitoid aggregation.
5. The natural variation in A. ervi mummy density is greatest at the larger scales of study. Therefore, density-dependent hyperparasitism occurs only when there is high natural variation in mummy density.     

Key to the New Zealand species of Psyllaephagus Ashmead (Hymenoptera: Encyrtidae) with descriptions of three new species and a new record of the psyllid hyperparasitoid Coccidoctonus psyllae Riek (Hymenoptera: Encyrtidae)

Abstract  This paper records seven species of wasps in the genus Psyllaephagus (Hymenoptera: Encyrtidae) from New Zealand. All of these species are primary parasitoids of psylloids (Hemiptera: Psylloidea). Two are species previously described from New Zealand: P. acaciae Noyes and P. pilosus Noyes. Two are described Australian species which have established recently: P. bliteus Riek and P. gemitus Riek. Three new species are described here, from New Zealand: P. breviramus sp. nov., P. cornwallensis sp. nov. and P. richardhenryi sp. nov. All species are probably Australian in origin. A key to all seven Psyllaephagus species known from New Zealand is provided. An earlier first record of the Australian psyllid hyperparasitoid Coccidoctonus psyllae Riek (Hymenoptera: Encyrtidae), previously first recorded from New Zealand in 2006, is noted.     

Reproductive characteristics of invasive hyperparasitoid Baeoanusia albifunicle have implications for the biological control of eucalypt pest Paropsis charybdis

Hyperparasitoids can impede the establishment of primary parasitoid biological control agents or limit their control capacity. Although modern quarantine practices generally prevent hyperparasitoids being introduced with biological control agents, introductions can occur via natural pathways or accidentally with incoming passengers and cargo. In New Zealand, Baeoanusia albifunicle Girault is a self-introduced hyperparasitoid of Enoggera nassaui Girault, an intentionally introduced control agent of the eucalypt pest Paropsis charybdis Stål. A self-introduced primary parasitoid, Neopolycystus insectifurax (Girault), also parasitises P. charybdis in New Zealand. We assessed B. albifunicle biology to better understand its potential to disrupt P. charybdis control. It was determined that B. albifunicle is an obligate solitary hyperparasitoid with a longer lifespan, lower fecundity and longer generation time than its host. The hyperparasitoid reduced effective parasitism by E. nassaui to <10% in the lab, indicating it may limit control of the first P. charybdis generation by slowing spring population growth. It was confirmed that N. insectifurax is not hyperparasitised by B. albifunicle and therefore has some potential to substitute for any hyperparasitoid-driven decline in E. nassaui.     

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.     

Parasites ofMonellia caryella [Hom.: Aphididae]: Phenology and effect on the aphid population in pecan orchards in Israel

One primary parasite,Trioxys pallidus (Haliday) (Hym.: Braconidae), and a secondary parasite,Aphidencyrtus sp., were identified from the blackmargined aphid,Monellia caryella (Fitch) (Hom.: Aphididae), in Israeli pecan orchards. The average total parasitism for all locations sampled was 13.5%. Although a hyperparasite was discovered, it had no significantly detrimental effect on the parasite. Contribution from the Agricultural Research Organization, The Volcani Center, Bet Dagan, Israel, No. 2034-E, 1987 series.     

蝇蛹俑小蜂对橘小实蝇和瓜实蝇的偏好性

【背景】蝇蛹俑小蜂是实蝇类害虫蛹期的一种重要寄生蜂,对压制下一代实蝇类害虫的种群数量具有重要作用,但有关其对不同实蝇害虫的寄生特性尚缺乏研究。【方法】采用"H"型装置和培养皿测定方法,研究了蝇蛹俑小蜂的寄主选择偏好性。【结果】蝇蛹俑小蜂在橘小实蝇蛹和瓜实蝇蛹共存的情况下,偏好在橘小实蝇蛹上停留,且寄生率较高,最高寄生率达61.11%。【结论与意义】本研究为合理利用蝇蛹俑小蜂控制实蝇类害虫提供了理论基础。     

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.