Parasitism rates and sex ratios of a parasitoid wasp: effects of herbivore and plant quality

Summary We studied interactions among collards, Brassica oleracea var. acephala, the diamondback moth (DBM), Plutella xylostella (Lepidoptera: Yponomeutidae) and its parasitoid Diadegma insulare (Hymenoptera: Ichneumonidae) by manipulating plant nitrogen (N) concentrations in field and laboratory experiments. Parasitoid abundance strongly reflected DBM abundance and was related to total leaf N. Parasitism rates were high (70.7%) and density-independent. Wasp sex ratios varied markedly (3–93% female) in response to the herbivores, the plants, or both. Higher proportions of female wasps emerged from DBM larvae on plants with high leaf N than on unfertilized plants. More female wasps also emerged from larvae parasitized as larger instars. We suggest that wasps have the potential to control DBM populations through long-term numerical responses mediated by variable sex ratios.     

Kin discrimination and sex ratios in a parasitoid wasp

Sex ratio theory provides a clear and simple way to test if nonsocial haplodiploid wasps can discriminate between kin and nonkin. Specifically, if females can discriminate siblings from nonrelatives, then they are expected to produce a higher proportion of daughters if they mate with a sibling. This prediction arises because in haplodiploids, inbreeding (sib-mating) causes a mother to be relatively more related to her daughters than her sons. Here we formally model this prediction for when multiple females lay eggs in a patch, and test it with the parasitoid wasp Nasonia vitripennis. Our results show that females do not adjust their sex ratio behaviour dependent upon whether they mate with a sibling or nonrelative, in response to either direct genetic or a range of indirect environmental cues. This suggests that females of N. vitripennis cannot discriminate between kin and nonkin. The implications of our results for the understanding of sex ratio and social evolution are discussed.     

Brood sex ratios of the solitary parasitoid wasp, Coccophagus atratus

Abstract.

• 1 Female eggs of Coccophagus atratus are deposited within the haemolymph of coccoid scale insects. Male eggs are deposited on to late larval and prepupal stages of parasitoids of scale insects, including conspecifics.
• 2 When presented with either one host type or a combination of both host types, female C.atratus deposit all their available eggs, assigning the appropriate sex egg to each host encountered. Brood sizes are not adjusted for different combinations of hosts.
• 3 Behavioural observations show that females do not move away from patches of hosts until all their eggs are laid, regardless of the host type.
• 4 Brood sex ratios varied with changes in the relative availability of hosts for males and hosts for females. When both host-types were present in equal numbers, male biased sex ratios resulted (mean ±SEM =0.71 ± 0.009) and when 70% of hosts provided were suitable for female eggs, mostly female-biased sex ratios resulted (mean ± SEM = 0.37±0.01).
• 5 Our results do not fit predictions based on the assumption that a sex ratio of 0.5 should be expected in C.atratus. Observed sex ratios indicate that the unusual life histories of these parasitoids need to be taken into account in explanations of their sex ratios.

     

Split sex ratios and virginity in a gall‐inducing thrips

Split sex ratios have been predicted in haplodiploid populations with high proportions of reproductive virgins, but there has been little empirical support. We found such split sex ratios in the gall‐inducing thrips, Kladothrips rugosus. Sex ratios of juveniles from 96 galls were determined using chaetotaxy over two consecutive summers. The population‐wide sex ratio was unbiased, but bimodal. Twenty‐four per cent of galls only contained male juveniles. These galls were induced by a female that was probably a virgin. The mean sex ratio of all other galls was 0.36 ± 0.02, which is not significantly different from the theoretical evolutionarily stable sex ratio of 0.34, calculated from a previous model ( 20 . J. Evol. Biol. 3 : 3–17) for 24% constrained females in a panmictic population. These data provide the first empirical support for the constrained sex allocation model of Godfray.     

A genetic perspective on mating systems and sex ratios of parasitoid wasps

Parasitoid sex ratios are influenced by mating systems, whether complete inbreeding, partial inbreeding, complete inbreeding avoidance, or production of all-male broods by unmated females. Population genetic theory demonstrates that inbreeding is possible in haplodiploids because the purging of deleterious and lethal mutations through haploid males reduces inbreeding depression. However, this purging does not act quickly for deleterious mutations or female-limited traits (e.g., fecundity, host searching, sex ratio). The relationship between sex ratio, inbreeding, and inbreeding depression has not been explored in depth in parasitoids. The gregarious egg parasitoid, Trichogramma pretiosum Riley, collected from Riverside, CA (USA) produced a female-biased sex ratio of 0.24 (proportion of males). Six generations of sibling mating in the laboratory uncovered considerable inbreeding depression (∼ 20%) in fecundity and sex ratio. A population genetic study (based upon allozymes) showed the population was inbred (F _it = 0.246), which corresponds to 56.6% sib-mating. However, average relatedness among females emerging from the same host egg was only 0.646, which is less than expected (0.75) if ovipositing females mate randomly. This lower relatedness could arise from inbreeding avoidance, multiple mating by females, or superparasitism. A review of the literature in general shows relatively low inbreeding depression in haplodiploid species, but indicates that inbreeding depression can be as high as that found in Drosophila. Finally, mating systems and inbreeding depression are thought to evolve in concert (in plants), but similar dynamic models of the joint evolution of sex ratio, mating systems, and inbreeding depression have not been developed for parasitoid wasps. Received: November 13, 1998 /Accepted: January 8, 1999     

Arthropod functional traits shaped by landscape-scale field size,local agri-environment schemes and edge effects

Agri-environment scheme (AES) approaches can be classified according to whether they prescribe management in non-productive areas, such as field boundaries and wildflower strips, or in productive areas, such as arable crops. Here we tested the ecological effectiveness of two popular AESs in Germany: wildflower strips next to winter wheat fields as off-field management and organic farming on winter wheat fields as on-field management. We selected ten landscapes along a field size gradient with three focal wheat fields, one conventional field with flower strip, one organic field and one conventional field without flower strip as a control. We sampled arthropods with pitfall traps at field edges and field interiors. We selected three ecological traits for spiders and carabids (body size, feeding trait, dispersal ability). We calculated community weighted mean values (CWM), and we used linear mixed effects models to test the effect of management type and transect position on CWM values. We found pronounced edge effects on most traits, and weaker effects of field size and AES in shaping functional traits. Smaller spiders, spiders with higher ballooning propensity and more web-builders were in the field interior than at the field edge, whereas carnivore carabids preferred field interiors. We also found a strong effect of landscape configuration, i.e. mean field size, as larger field size was positively related to more web-building spiders and more carnivore beetles. Flower strips enhanced populations of web-building spiders. Our results suggest that small-scale agriculture leading to high landscape-scale edge density has a major effect in shaping functional traits and potential ecosystems services in agricultural landscapes. Spider and carabid communities exhibit very different responses to edge vs. interior sites, and, based on the landscape-scale field size gradient emphasize the importance of landscape configuration in shaping the heterogeneity of the arthropods’ traits and presumably ecosystem services in agricultural landscapes.     

Population sex ratios, sex-specific clonal traits and tradeoffs among these traits in the liverwort Marchantia inflexa

Unisexual, female- or male-biased populations are common among some clonal plants. Within and among populations, the relative frequencies of males and females can be influenced by sex-specific demographic patterns that, in turn, can be a consequence of life-history characteristics. The objectives of this study were to describe (1)  population sex-ratio patterns among habitat patches along a river, and (2)  sex-specific patterns of and correlations among life-history clonal traits including: growth rates, number of meristematic tips and asexual reproduction in the dioecious liverwort, Marchantia inflexa . In Trinidad, a section of a stream was surveyed for the occurrence of female and male sex expressing thalli among habitat patches, and habitat characteristics (canopy openness and patch size) were recorded. The numbers of female and male inflorescences were obtained also. Of the 209 patches observed in the field, 83% did not contain sex expressing thalli, 9% contained thalli of both sexes, and the rest contained only female- (4%) or male-expressing (4%) thalli. Sex expression was less common among small patches, and there was a tendency for sex expression to be less likely among patches with the lowest canopy openness. The proportion of male inflorescences among the bisexual patches ranged from 0.22 to 0.80. In a greenhouse, we planted gemmae (asexual propagules) from field-collected isolates: ten female and eight male. On six occasions, we harvested replicates of each isolate to estimate isolate trait means. Females grew faster, produced more meristematic tips and had lower levels of asexual reproduction than males. Number of meristematic tips was negatively correlated with asexual reproduction and positively correlated with growth rate. These sex-specific patterns may lead to the high frequency of single sex patches as well as biased adult population sex ratios that are observed in the field.     

Sex allocation and effects of superparasitism on secondary sex ratios in the gregarious parasitoid, Trichogramma chilonis (Hymenoptera: Trichogrammatidae)

The role of sex-controlling behaviour at oviposition in generating primary sex ratios, and the effect of larval competition on secondary sex ratios, were studied in the gregarious endoparasitoid, Trichogramma chilonis. The production of a fertilized (female) egg is indicated by the incorporation of a pause in abdominal movements during oviposition, while the absence of it indicates the production of an unfertilized (male) egg. During each ovipositional bout, the first male egg is deposited at the second oviposition, and thereafter at intervals of about eight eggs. This simple pattern enables the wasps to adjust their progeny sex ratios under local male competition to a wide range of host size. Inexperienced wasps do not distinguish between parasitized and healthy hosts. Immature mortality is not significantly different between the sexes when a host is attacked by a single wasp, while females suffer higher immature mortality than males when superparasitism occurs.     

Sex ratios under asymmetrical local mate competition: theory and a test with parasitoid wasps

Sex ratio theory allows unparalleled opportunities for testing how well animal behavior can be predicted by evolutionary theory. For example, Hamilton's theory of local mate competition (LMC) is well understood and can explain variation in sex allocation across numerous species. This allows more specific predictions to be developed and tested. Here we extend LMC theory to a situation that will be common in a range of species: asymmetrical LMC. Asymmetrical LMC occurs when females lay eggs on a patch asynchronously and male offspring do not disperse, leading to relatively weaker LMC for males emerging from later broods. Varying levels of LMC then lead to varying optimal sex ratios for females, depending on when and where they oviposit. We confirm the assumptions of our theory using the wasp Nasonia vitripennis and then test our predictions. We show that females adjust their offspring sex ratios in the directions predicted, laying different sex ratios on different hosts within a patch. Specifically, there was a less female-biased sex ratio when ovipositing on an unparasitized host if another host on the patch had previously been parasitized and a less female-biased sex ratio on parasitized hosts if females also oviposited on an unparasitized host.     

Female-biased sex ratios under local mate competition: An experimental confirmation

Summary Experimental work of Nadel and Luck (1992) on a chalcidoid wasp provides a confirmation of sex ratio theory under local mate competition.     

Unisexual broods and sex ratios in a polyembryonic encyrtid parasitoid (Copidosoma sp.: Hymenoptera)

Summary We examined brood sex ratios of an undetermined species of Copidosoma. Most broods (65%) were unisexual, with a greater proportion of female broods. Some mixed broods contained extremely small proportions of wasps of the opposite sex. Our results imply that the female-biased sex rations in this species cannot be explained by local mate competition theory.     

Evolution of sex ratios in social hymenoptera: kin selection,local mate competition,polyandry and kin recognition

A model is constructed to study the effects of local mate competition and multiple mating on the optimum allocation of resources between the male and female reproductive brood in social hymenopteran colonies from the ‘points of view’ of the queen (parental manipulation theory) as well as the workers (kin selection theory). Competition between pairs of alleles specifying different sex investment ratios is investigated in a game theoretic frame work. All other things being equal, local mate competition shifts the sex allocation ratio in favour of females both under queen and worker control. While multiple mating has no effect on the queen’s optimum investment ratio, it leads to a relatively male biased investment ratio under worker control. Under queen control a true Evolutionarily Stable Strategy(ess) does not exist but the ‘best’ strategy is merely immune from extinction. A trueess exists under worker control in colonies with singly mated queens but there is an asymmetry between the dominant and recessive alleles so that for some values of sex ratio a recessive allele goes to fixation but a dominant allele with the same properties fails to do so. Under multiple mating, again, a trueess does not exist but a frequency dependent region emerges. The best strategy here is one that is guaranteed fixation against any competing allele with a lower relative frequency. Our results emphasize the need to determine levels of local mate competition and multiple mating before drawing any conclusions regarding the outcome of queen-worker conflict in social hymenoptera. Multiple mating followed by sperm mixing, both of which are known to occur in social hymenoptera, lower average genetic relatedness between workers and their reproductive sisters. This not only shifts the optimum sex ratio from the workers’ ‘point of view’ in favour of males but also poses problems for the kin selection theory. We show that kin recognition resulting in the ability to invest in full but not in half sisters reverts the sex ratio back to that in the case of single mating and thus completely overcomes the hurdles for the operation of kin selection.     

Evolution of extraordinary female-biased sex ratios: the optimal schedule of sex ratio in local mate competition

Female-biased sex ratio in local mate competition has been well studied both theoretically and experimentally. However, some experimental data show more female-biased sex ratios than the theoretical predictions by Hamilton [1967. Science 156, 477-488] and its descendants. Here we consider the following two effects: (1) lethal male-male combat and (2) time-dependent control (or schedule) of sex ratio. The former is denoted by a male mortality being an increasing function of the number of males. The optimal schedule is analytically obtained as an evolutionarily stable strategy (ESS) by using Pontrjagin's maximum principle. As a result, an ESS is a schedule where only males are produced first, then the proportion of females are gradually increased, and finally only females are produced. Total sex ratio (sex ratio averaged over the whole reproduction period) is more female-biased than the Hamilton's result if and only if the two effects work together. The bias is stronger when lethal male combat is severer or a reproduction period is longer. When male-male combat is very severe, the sex ratio can be extraordinary female-biased (less than 5%). The model assumptions and the results generally agree with experimental data on Melittobia wasps in which extraordinary female-biased sex ratio is observed. Our study might provide a new basis for the evolution of female-biased sex ratios in local mate competition.     

Local resource competition and local resource enhancement shape primate birth sex ratios

Sex ratio theory provides a powerful source of testable predictions about sex allocation strategies. Although studies of invertebrates generally support predictions derived from the sex ratio theory, evidence for adaptive sex ratio biasing in vertebrates remains contentious. This may be due to the fact that most studies of vertebrates have focused on facultative adjustment in relation to maternal condition, rather than processes that might produce uniform sex biases across individuals. Here, we examine the effects of local resource enhancement (LRE) and local resource competition (LRC) on birth sex ratios (BSRs). We also examine the effects of sex differences in the costs of rearing male and female offspring on BSRs. We present data from 102 primate species and show that BSRs are skewed in favour of the dispersing sex in species that do not breed cooperatively, as predicted by the LRC model. In accordance with the LRE model, BSRs are generally skewed in favour of the more beneficial sex in cooperatively breeding primate species. There is no evidence that BSRs reflect the extent of sexual size dimorphism, an indirect measure of the costs of rearing male and female offspring. These analyses suggest that adaptive processes may play an important role in the evolution of BSRs in vertebrates.     

The influence of host size on sex ratios in the parasitoid Diglyphus begini (Hymenoptera: Eulophidae)

Abstract. 1. Sex ratio in the ectoparasitoid, Diglyphus begini (Ashmead), attacking larvae of the dipterous leafminer Liriomyza trifolii (Burgess) in glasshouse marigolds, is best depicted by a model where sex ratio varies as a function of host size.
2. Male D. begini progeny are produced in hosts significantly smaller in size than those producing female progeny.
3. Female wasps attack and oviposit on the largest leafminer larvae available and whether a host is large or small depends upon the size of the other hosts attacked.
4. Diglyphus begini females adjust the thre:shold size for the change-over in sex allocation relative to the size of hosts attacked; however, the sex ratio is maintained at between 60% and 70% males.
5. The patterns observed in these glasshouse studies are not due to sex-specific differential mortality or superparasitism.