Host population structure affects field sex ratios of the heteronomous hyperparasitoid, Coccophagus atratus

Abstract.

• 1 Second instar Filippia gemina de Lotto scale insects are the preferred hosts of female Coccophugus atrutus Compere larvae. These scale insects were found on their host plants, Chrysanthemoides monilifera Norlindh and Cliffortia strobilifera Mettenius, only at certain times during a 1 year sampling programme.
• 2 Late larval instars and prepupae of C.atratus, and a Metaphycus species, are the preferred hosts of male C.atratus larvae. These hosts, although they occurred on the same host plants as hosts for female C.atratus, were most numerous at different times during the sampling period.
• 3 The ratio of hosts suitable for C.atratus varied from a predominance of hosts suitable for females through to a predominance of hosts suitable for males. Sex ratios of adult C.atratus followed a similar trend but did not reflect, exactly, the ratio of available hosts. Differences in mortality between sexes and hyperparasitism may account for this anomaly.
• 4 Variable population sex ratios observed in C.atratus apparently result from the behaviour of individual females in which brood sex ratios are dependent on the relative availability of hosts for males and hosts for females. This behaviour, in turn, may result from variability in the host population structure but may also result from selection pressures operating at the time that heteronomous hyperparasitism evolved.

     

寄主大小及寄生顺序对蝇蛹佣小蜂寄生策略的影响

寄主大小模型认为寄生蜂后代性比与寄主大小相关,寄生蜂倾向于在大寄主上产出更多雌性后代,在小寄主上产出更多雄性后代.探讨了以家蝇蛹为寄主时,蝇蛹佣小蜂后代产量和性比变化;单次寄生情况下,寄主大小及寄生顺序对寄生蜂后代性比等影响.结果表明,蝇蛹佣小蜂的产卵期为(8.93±3.34)d,单头雌蜂能产雌性后代(34.11±16.34)头和雄性后代(11.04±8.87)头,且雄性百分比为0.24±0.11.随成蜂日龄的增大,寄生蜂产生雄性后代的比率显著增加.蝇蛹佣小蜂在寄生家蝇蛹时,会优先选择寄生个体较大的蛹;在单次寄生的情况下,蝇蛹佣小蜂倾向于在较大的家蝇蛹内产出更多的雌性后代.     

The developmental strategies and related profitability of an idiobiont ectoparasitoid Sclerodermus pupariae vary with host size

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The reproductive strategy of the gregarious parasitoid,Pteromalus puparum (Hymenoptera: Pteromalidae)

Summary Pteromalus puparum is a gregarious parasitoid of many butterfly pupae. Adult size, mortality, and sex ratio of P. puparum, as a parasitoid of Papilio xuthus, were unit weight of the host. Effects of female size on fecundity, wing load, and longevity were also examined.The highest total weight of progeny from the host was attained when the number of eggs per gram of the host was approximately 150. Positive correlations were observed between the size of the females and their fecundity and wing load. The maximum longevity of the female kept with honey but without hosts was attained when the initial number of parasitoids per g of the host was 150.Considering the total fecundity of all female progeny, the reproductively most efficient number of eggs to be deposited per g of the host was estimated to be approximately 300. However, as shortage of food for the adult females strongly affects their fecundity, the reproductively most efficient number of eggs to be deposited per g of the host was about 70 when the adult female progeny was not provided with food.The optimal number of eggs to be deposited when the emale oviposits in the host under field conditions is discussed.     

Preference of an exotic wood borer for stressed trees is more attributable to pre‐alighting than post‐alighting behaviour

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Impact of mating on Anagyrus kamali Moursi (Hym., Encyrtidae) lifetime fecundity, reproductive longevity, progeny emergence and sex ratio

Abstract: The solitary endoparasitoid Anagyrus kamali Moursi (Hym., Encyrtidae) and the Hibiscus mealybug Maconellicoccus hirsutus Green (Hom., Pseudococcidae), were used as a parasite/host model to test the effect of mating on several fitness parameters, i.e. longevity, lifetime fecundity, progeny emergence and sex ratio. At 27 ± 2°C, 8 h light : 16 h dark, mating significantly affected the survival of male parasitoids. Virgin males lived longer (32.2 ± 9.51 days) than mated males (23.9 ± 7.52 days). Female longevity (40.7 ± 16.3 days for virgins and 36.2 ± 10.7 days for mated females) was not affected by mating. The lifetime fecundity of female parasitoids and their oviposition period was not significantly affected by mating. However, the number of hosts parasitized was greater for mated wasps (7.54 ± 4.85 hosts parasitized/day) compared with virgin ones (5.12 ± 2.19 hosts parasitized/day). This resulted in greater progeny production from mated A. kamali females. The progeny of virgin females consisted only of males, whereas the mated ones had a more female‐biased sex ratio. The lowest sex ratio (0.41 M/F ± 0.123) was attained when females had free access to males and were multi‐mated.     

Brood guarding in a bethylid wasp

Abstract.

• 1 Atypical of the parasitoid Hymenoptera, female Goniozus nephantidis Muesebeck remain with offspring until they pupate. This behaviour will only have evolved if the consequent reduction in fecundity is outweighed by fitness returns.
• 2 G.nephantidis competes for hosts with conspecific and non-conspecific parasitoids. The effectiveness of G.nephantidis at deterring superparasitism and multiparasitism is tested. Brood survivorships were compared when G.nephantidis and Bracon hebetor Say intrude on hosts with the mother present and absent and with offspring at different developmental stages.
• 3 Laying by the intruder reduced brood survivorship. Guarding reduced oviposition on unparasitized hosts by intruding females, and prevented superparasitism of hosts with egg broods. Hosts with larval broods were rarely superparasitized. Multiparasitism was common except on hosts with guarded larval broods, but even here survivorship was reduced.
• 4 Competitive asymmetries determined the outcome of contests for possession of host resources.
• 5 The costs of remaining seem at least partially offset by the prevention of oviposition by competing parasitoids.

     

Effect of host availability on reproduction and survival of the parasitoid wasp Trichogramma minutum

Abstract.

• 1 We tested the hypothesis that females of the egg parasitoid, Trichogramma minutum Riley (Hymenoptera: Trichogrammatidae), could adjust their fecundity schedule according to host availability and that there was a negative correlation between reproduction and survival in these wasps.
• 2 Newly-emerged females were provided with an unlimited or limited number of hosts in the first trial and with either unlimited, limited or zero hosts in the second trial.
• 3 When hosts were unlimited, wasps had the highest rate of reproduction in the first day, which decreased dramatically thereafter. When hosts were limited, wasps from the two trials differed in their response. In Trial I, females with limited hosts had lower first-day fecundity than, and the same subsequent-day fecundity as, those with unlimited hosts. However, in Trial II, females with limited host had a lower first-day but a higher subsequent-day fecundity than those with unlimited hosts. This indicates variation in Trichogramma's ability to shift its fecundity schedule in response to host availability.
• 4 There was a positive (rather than a negative) correlation between reproduction and survival. Wasps that oviposited (in host-unlimited treatment) had greater longevity than those that could not (in host-unavailable treatment).
• 5 The sex ratio of the progeny produced by wasps in both host-unlimited and limited treatments shifted gradually from a female to a male bias as the wasps aged.
• 6 We consider the ability of parasitoids to adjust their fecundity schedule as an adaptation to changing host resources and discuss our findings with regard to theories of life history evolution.

     

Impact of mating status on egg-laying and superparasitism behaviour in a parasitoid wasp

Most parasitoid female wasps can distinguish between unparasitized and parasitized hosts and use this information to optimize their progeny and sex allocation. In this study, we explored the impact of mating on oviposition behaviour (parasitism and self‐ and conspecific superparasitism) on both unparasitized and already parasitized hosts in the solitary parasitoid wasp Eupelmus vuilleti (Crw.) (Hymenoptera: Eupelmidae). Virgin and mated females had the same oviposition behaviour and laid eggs preferentially on unparasitized hosts. The sex ratio (as the proportion of females) of eggs laid by mated females in parasitism and conspecific superparasitism was 0.67 ± 0.04 and 0.57 ± 0.09, respectively. Likewise, females laid more eggs in conspecific superparasitism than self‐superparasitism under our experimental conditions. These experiments demonstrate that E. vuilleti females can (i) discriminate between unparasitized and parasitized hosts and adapt the number of eggs they lay accordingly, and (ii) probably discriminate self from conspecific superparasitized hosts. Finally, mating does not appear to influence the host discrimination capacity, the ovarian function, or the oviposition behaviour.     

Sex Allocation Decision Under Superparasitism by the Parasitoid Wasp Eupelmus vuilleti

Superparasitism is a widespread phenomenon in parasitoids and may be advantageous in some circumstances. In this study, offspring sex ratio was analysed in three superparasitism situations: when the second egg was laid by a random Eupelmus vuilleti (Hymenoptera: Eupelmidae) female from a group, when an isolated female was allowed to lay two eggs on the same host (self-superparasitism) or laid one egg on a host already parasitized by a conspecific (conspecific superparasitism). Females produced a different offspring sex ratio according to the different superparasitism situations tested. These sex ratios are in line with the local mate competition theory. The results further suggest that females can discriminate between hosts parasitized by a conspecific or by themselves and adapt the sex of the eggs they lay accordingly.     

A sex ratio theory of gregarious parasitoids

Summary A mathematical model is constructed to explain a density-dependent increase in the progeny sex ratios of gregarious parasitoids. In the model we considered non-cooperative game between females concerned with their own inclusive fitness. Equilibrium progeny sex ratios of the first and second females ovipositing on the same host are expressed in terms of the probability of double parasitism (p), the ratio of a male to a female in contribution to resource competition (α), the clutch size ratio between the two females (β), the crowding effect on female reproductive success (γ), and the inbreeding coefficient (f). Major predictions from the model are: 1) the progeny sex ratios of both the first and second females increase withp, 2) as β becomes smaller, the progeny sex ratios of the first females decrease, while those of the second females dramatically increases, 3) when a host is attacked by at most two wasps, the sex ratio of the total number of eggs laid on the host does not exceed 0.25. The effects of α and preferential death by female progeny in doubly parasitized hosts are considered as factors responsible for an excess number of males at emergence. Some possible modes of density-dependent increase in the sex ratios of the overall progeny populations is also discussed on the basis of the present model.     

Geographic variation in reproductive success of the parasitoid Asobara tabida in larvae of several Drosophila species

Abstract.

• 1 Asobara tabida is a parasitoid of Drosophila larvae in fermenting substrates. Because it is a widespread species, it may encounter different biotic and abiotic circumstances in various parts of its range.
• 2 The species composition of the host population varies over the parasitoid's range: D.obscura-group species (especially D.subobscura) are the main hosts for northwestern and central European parasitoids; D.melanogaster is the main host for southern European parasitoids.
• 3 D.melanogaster larvae can defend themselves against A.tabida by encapsulating the parasitoid egg, and survival in D.melanogaster is always lower than in D.subobscura.
• 4 Parasitoids from southern European populations are much better able to survive in D.melanogaster than their northwestern and central European conspecifics; parasitoids from different populations are equally well able to survive in D.subobscura.
• 5 The lower survival in D.melanogaster may be partly compensated for by the larger size of parasitoids emerging from this host species compared to parasitoids emerging from D.subobscura.
• 6 Within population groups, larger A.tabida females have more eggs in their ovarioles. Additionally, southern European females have more eggs and less fat than northern and western/central European females. The relationship between size and longevity is ambiguous.
• 7 It is concluded that parasitoids from different populations are adapted to region-specific circumstances.

     

The effect of host developmental stage at parasitism on sex‐related size differentiation in a larval endoparasitoid

• 1 For their larval development, parasitoids depend on the quality and quantity of resources provided by a single host. Therefore, a close relationship is predicted between the size of the host at parasitism and the size of the emerging adult wasp. This relationship is less clear for koinobiont than for idiobiont parasitoids.
• 2 As size differentiation in host species exhibiting sexual size dimorphism (SSD) is likely to occur already during larval development, in koinobiont larval endoparasitoids the size of the emerging adult may also be constrained based on the sex of the host caterpillar.
• 3 Sex‐specific growth trajectories were compared in unparasitised Plutella xylostella caterpillars and in second and fourth instar hosts that were parasitised by the solitary larval koinobiont endoparasitoid Diadegma semiclausum. Both species exhibit SSD, where females are significantly larger than males.
• 4 Healthy female P. xylostella caterpillars developed significantly faster than their male conspecifics. Host regulation induced by D. semiclausum parasitism depended on the instar attacked. Parasitism in second‐instar caterpillars reduced growth compared to healthy unparasitised caterpillars, whereas parasitism in fourth‐instar caterpillars arrested development. The reduction in growth was most pronounced in hosts producing male D. semiclausum.
• 5 Parasitism itself had the largest impact on host growth. SSD in the parasitoid is mainly the result of differences in growth rate of the parasitoid–host complex producing male and female wasps and differences in exploitation of the host resources. Female wasps converted host biomass more efficiently into adult biomass than males.

     

Genetic variability in the reactive distance inTrichogramma brassicae after automatic tracking of the walking path

Efficiency of hymenopterous parasitoids to control pests in a biological control release program probably increases with increasing searching ability of the females, which, in return, likely depends on the distance from which females perceive their hosts (i.e., reactive distance). In this study, we first analyse this hypothesis with the help of a stochastic model simulating the walking path of isolatedTrichogramma females during their searching behaviour. Then, this reactive distance is estimated using automatic recording and analysis of the walking path of female wasps. Finally, the genetic variability for this trait is analysed in aTrichogramma brassicae Bezdenko (Hym.; Trichogrammatidae) population. Three types of hosts were used: Eggs ofEphestia kuehniella Zeller (Lep.; Pyralidae), eggs ofMamestra brassicae L. (Lep.; Noctuidae) and 0.45 mm glass beads.M. brassicae eggs are perceived from 4.01±0.15 mm, which is a significantly longer perceptive distance than forE. kuehniella eggs (3.69±0.10 mm) and glass beads (3.67±0.10 mm). Moreover, whatever the host tested, a significant genetic variation is observed in this trait in the population studied. The ecological and evolutionary implications and the agronomical importance of these results are discussed.     

Host selection by Ibalia leucospoides based on temporal variations of volatiles from the hosts’ fungal symbiont

Insect parasitoids locate hosts via reliable and predictable cues such as volatile emissions from hosts and/or host plants. For insects that depend on mutualistic organisms, such as many wood‐boring insects, symbiont‐derived semiochemicals may represent a source of such cues to be exploited by natural enemies. Ultimately, exploitation of these signals may increase fitness by optimizing foraging efficiency. Female parasitoids of Ibalia leucospoides use volatiles from the fungal symbiont Amylostereum areolatum of their host Sirex noctlio to find concealed host eggs and young larvae within the xylem. We hypothesize that the temporal pattern of fungal emissions may indicate not only the presence of host larvae but also be used as a cue that indicates host suitability and age. Such information would allow female parasitoids to discern more efficiently between hosts within ovipositor reach from those already buried too deep into the xylem and out of reach. In this context, we assessed the behaviour of I. leucospoides females to volatiles of A. areolatum in a ‘Y’‐tube olfactometer at regular intervals over 30 days. We concurrently examined the fungal volatiles by headspace sampling through solid‐phase microextraction (SPME) followed by gas chromatography mass spectrometry (GC‐MS). We observed that females were attracted to volatiles produced by two‐week‐old fungal cultures, a period that matches when older larvae are still within ovipositor reach. Four chemical compounds were detected: ethanol, acetone, acetaldehyde and the sesquiterpene 2,2,8‐trimethyltricyclo[6.2.2.01,6]dodec‐5‐ene, with each compounds’ relative abundance changing over time. Results are discussed in the context of parasitoids fitness. Future studies involving electrophysiology, different collection techniques and further behavioural assays will help in identifying the compounds that convey temporal information to female parasitoids and have the potential for being used in integrated pest management programmes.     

Factors affecting sex ratio in rearing ofCoeloides sordidator (Hym.: Braconidae)

Five factors known to affect the sex ratio (% of males) in parasitic Hymenoptera were investigated forCoeloides sordidator, a parasitoid ofPissodes weevils. The host age, the age of ovipositing females, and the host of origin had a significant impact on the sex ratio of offspring. In contrast, the number of ovipositing females had an insignificant effect on sex ratio whereas the effect of host density could not be clearly defined. The sex ratio decreased with host age, probably because, like many other hymenopteran parasitoids, females tend to lay male eggs on small hosts and female eggs on larger hosts in order to maximize the size and fitness of their female offspring. The sex ratio also varied with the age of the mother, younger females laying more male eggs and older females more female eggs. The host of origin also had an influence on sex ratio. The strain fromPissodes castaneus was significantly more male-biased than the strain fromP. validirostris, which corroborates previous observations made on field populations     

Bionomics of Opius bellus (Hymenoptera: Braconidae), an endoparasitoid of Anastrepha fraterculus (Diptera: Tephritidae) in fruit-growing areas of Northwestern Argentina

Opius bellus is a neotropical larval-prepupal parasitoid known to attack the pestiferous fruit fly, Anastrepha fraterculus. Due to interest in the use of native parasitoids in forthcoming fruit fly biocontrol programmes in Argentina, O. bellus was colonised for the first time using laboratory-reared A. fraterculus larvae. A series of experiments were conducted to (1) best achieve an efficient parasitoid rearing by determining optimal larval host age, host:parasitoid ratio and host exposure time and (2) assess their potential as biological control agents by determining reproductive parameters. The most productive exposure regimen was: 7–9 d-old (early and middle third-instars) A. fraterculus larvae for 4 h at a 4:1 host:parasitoid ratio; this array of factors was sufficient to achieve the highest average adult emergence (48%) and an offspring sex ratio at equitable proportion. Increasing both host:parasitoid ratio further than 4:1 and the host exposure time beyond 4 h did not significantly enhance parasitoid female offspring yield. Females produced eggs for 29.5 ± 1.4 days. At 32 days of age, 50% of the females were still alive. The majority of the progeny were produced by females between 20 and 24 d-old. At 26°C, gross fecundity rate, net reproductive rate, intrinsic rate of increase and mean generation time were 20.7 ± 4.2 offspring/female, 9.6 ± 2.5 females/newborn females, 0.06 ± 0.01 females/female/day and 8.4 ± 0.2 days, respectively. The long lifespan and reproductive parameters suggest that this parasitoid species has suitable attributes for mass-rearing.     

Parasitism and oviposition of Melittobia acasta on Bombus terrestris: Impact of larval overwintering and host status on pupation and adult emergence

Melittobia acasta (Walker) are microhymenopteran ectoparasitoids of the pupae and prepupae of the commercially‐used pollinator bumblebee species Bombus terrestris L. The female parasitoids puncture the host cuticle with their sting and feed oozing hemolymph. This study shows that M. acasta parasitize 100% pupae and 84% prepupae of B. terrestris but are ineffective on the larvae of the bees. The female parasitoids lay a significantly higher number of eggs on pupae (67.7 ± 16.2 female^?1) compared to prepupae (20.5 ± 14.5 female^?1). The parasitoids differ in their choice for oviposition sites and fecundity on different locations of B. terrestris pupae, and they show most preference for oviposition (32%) as well as fecundity (34.9 ± 15.1 female^?1) on the petiole of the host. Larvae of the parasitoids overwinter at low temperatures but larval overwintering duration and post‐diapause rearing on original or new hosts do not affect their pupation and adult emergence. Larvae have a higher percentage of pupation (88.0–94.4%) and adult emergence (84.4–92.9%) both on the original and the new host, thus indicate that the parasitoids are highly capable of reproduction in B. terrestris colonies.     

Host discrimination of a larval parasitoid: the quick movement of Microplitis demolitor

Many parasitoids discriminate previously parasitised hosts from unparasitised ones to avoid mortality of offspring. Parasitoids that parasitise aggressive hosts such as lepidopteran larvae are known to attack hosts very quickly to avoid being attacked. However, little is known about host discrimination of such quick attacking parasitoids. We investigated host discrimination of Microplitis demolitor (Wilkinson) (Hymenoptera: Braconidae) a quick attacking parasitoid of Helicoverpa armigera (Hübner) (Lepidoptera: Noctuidae). Results showed that ratios of female wasps that rejected the hosts after antennal examination did not differ between parasitised and unparasitised hosts, indicating that M. demolitor did not discriminate hosts by antennal examination. However, 95% of females that inserted ovipositor into unparasitised hosts actually laid eggs, whereas it was only 31% for parasitised hosts, indicating that females discriminated hosts by oviposition insertion. Analyzing video recordings revealed that the ovipositor exploration of the host took 0.3 s. Female wasps that had experienced high-host density of unparasitised hosts readily rejected parasitised hosts, while wasps with experience of low host availability of parasitised hosts tended to accept parasitised hosts. This suggests that host discrimination behaviour of M. demolitor is affected by previous experience of different host availability and host quality.

     

Sex ratios in field populations of Epidinocarsis lopezi, an exotic parasitoid of the cassava mealybug, in Africa

Abstract.

• 1 In cassava fields in Africa, population sex ratios of Epidinocarsis fopezi vaned from 0.44 (males to total parasitoids) at low host densities to highly male-biased ratios of 0.70 at high host densities.
• 2 This variability is caused by the difference in allocation of sons and daughters to hosts of different sizes, through the following mechanisms: (a) small, i.e. second instar, hosts are mainly used for the production of male offspring, whereas in large, i.e. third instar, hosts a variable, female-biased sex ratio is produced; (b) E.fopezi does not selectively oviposit into large hosts but always accepts both small and large hosts for oviposition upon encountering; (c) in the field, this parasitoid is time-limited, and not egg-limited. On the basis of an optimal diet model, such general host acceptance is shown to be the best strategy.
• 3 Thus, sex ratio increases with host density for three reasons: the proportion of small hosts encountered in the field increases with increasing host density, small hosts are used for male production, and hosts are always accepted when encountered.