母代雌蜂数、进果时间及非传粉小蜂对传粉榕小蜂后代数量及性比的影响

【目的】对性比的研究有助于我们理解自然界生物的选择压力及其所产生的原因和结果,榕树和榕小蜂之间的互惠共生关系以及生物学和生态学特性使其成为研究性比和局域配偶竞争模型（local mate competition）的理想材料。本研究旨在探明榕小蜂性比调节和进化机制。【方法】对分布于西双版纳地区的鸡嗉子榕Ficus semicordata进行了人工控制性放蜂实验。测定了母代雌蜂数量及其进果时间间隔、非传粉小蜂Sycoscapter trifemmensis数量对传粉榕小蜂Ceratosolen gravelyi后代数量（成蜂数量）和性比的影响,并分析了小蜂后代数量和性比的相关性。【结果】在榕果发育期一致的前提下,随着母代雌蜂数量的增加,每头雌蜂的平均后代数量明显下降(P<0.001),后代性比显著升高(P<0.001),后代数量和性比呈显著负相关(P<0.05);随着雌蜂进果间隔的延长,后代数量亦呈现下降趋势,且性比增大,放2头雌蜂和3头雌蜂的处理呈同样趋势,但差异均不显著(P=0.87; P=0.49),小蜂后代数量与性比无显著相关性(P=0.86)。此外,非传粉小蜂数量与传粉小蜂后代数量呈显著负相关(P<0.001),与传粉小蜂性比呈正相关(P<0.001),小蜂后代数量和性比同样呈现显著负相关(P<0.001)。【结论】本实验模拟了自然界中榕 蜂的相互作用,所得结果有助于我们理解自然状态下榕小蜂性比调节模式和机制,以及榕 蜂互利共生系统的进化机制。     

Clutch size, development and wing morph differentiation of Melittobia digitata

Melittobia digitata Dahms (Hymenoptera, Eulophidae) is a wing polymorphic, gregarious ectoparasitoid of bees and wasps. In nature, females of this wasp start to produce their progeny after feeding on the host. The first adults to develop will emerge as short wing morphs (SWM). Mother and daughters will lay eggs in the same hosts, and the following females to develop will emerge as long wing morphs (LWM). We evaluated the effects of the clutch size on the development, egg load, and wing morph differentiation of M. digitata. Developmental time was shorter when insects developed in small clutches, and immature survivorship was reduced in the largest clutch (400 eggs/host). Morph differentiation was also affected by the clutch size. SWMs developed in small clutches (5 and 25 eggs/host) while LWMs in large clutches (200 and 400 eggs/host). However, both morphs developed in intermediate clutches (50 and 100 eggs/clutch), with a decreasing number of SWMs developing with the increase in the clutch. The size and egg load of each morph was affected with the increase in the clutch size, although the forewing length/hind-tibia length ratio was kept constant for each morph developing from different clutch sizes. Egg load of LWMs was also reduced when compared to the SWMs that developed from the same clutch, although LWMs females were larger (longer tibia length). We discuss the possible mechanisms inducing the morph differentiation in M. digitata, as well as the physiological, behavioral, and ecological changes facing each morph.     

The mechanism of sex ratio adjustment in a pollinating fig wasp

Sex ratio strategies in species subject to local mate competition (LMC), and in particular their fit to quantitative theoretical predictions, provide insight into constraints upon adaptation. Pollinating fig wasps are widely used in such studies because their ecology resembles theory assumptions, but the cues used by foundresses to assess potential LMC have not previously been determined. We show that Liporrhopalum tentacularis females (foundresses) use their clutch size as a cue. First, we make use of species ecology (foundresses lay multiple clutches, with second clutches smaller than first) to show that increases in sex ratio in multi-foundress figs occur only when foundresses are oviposition site limited, i.e. that there is no direct response to foundress density. Second, we introduce a novel technique to quantify foundress oviposition sequences and show, consistent with the theoretical predictions concerning clutch size-only strategies, that they produce mainly male offspring at the start of bouts, followed by mostly females interspersed by a few males. We then discuss the implications of our findings for our understanding of the limits of the ability of natural selection to produce 'perfect' organisms, and for our understanding of when different cue use patterns evolve.     

Offspring production and development in the parasitoid wasp Melittobia clavicornis (Cameron) (Hymenoptera: Eulophidae) from Japan

The development time, sex ratio and offspring production of Melittobia clavicornis reared with wild, facultative and factitious hosts are presented. Known hosts and different biological aspects presented in previously published reports are summarized and clarified. Immature development time was equivalent or slightly longer than that of other Melittobia species, and the sex ratio was approximately 97% female. Total offspring numbers were considerably lower than that of other Melittobia species using the same hosts. We report female dimorphism in this species for the first time. The number and relative proportion of brachypterous morph females produced was higher than that in other species of the genus.     

Sex allocation and clutch size in parasitoid wasps that produce single-sex broods

The parasitoid wasp genus Achrysocharoides (Eulophidae) is unusual in that many of its species lay male and female eggs in single-sex clutches. The average clutch size of female broods is always greater than that of male broods, and in some species male clutch size is always one. We constructed models that predicted that severely egg-limited wasps should produce equal numbers of male and female eggs while severely host-limited wasps should produce equal numbers of male and female broods (and hence an overall female-biased sex ratio). Theory is developed to predict clutch size and sex ratio across the complete spectrum of host and egg limitation. A comparison of 19 surveys of clutch composition in seven species of Achrysocharoides showed a general pattern of equal numbers of male and female broods with a female-biased sex ratio (suggesting host limitation) although with considerable heterogeneity amongst collections and with a number of cases of unexpectedly low frequencies of male broods. Using a previous estimate of the relationship between fitness and size in the field, we predicted the maximally productive (Lack) clutch size for female broods of Achrysocharoides zwoelferi to be three. Of clutches observed in nature, 95% were equal to or smaller in size than the predicted Lack clutch size. When we manipulated local host density in the field, and as predicted by our models, clutch size and the proportion of female broods of A. zwoelferi decreased as hosts became more common, but the absolute frequency of male clutches was lower than expected. Copyright 1998 The Association for the Study of Animal Behaviour.     

TESTING MODELS OF FACULTATIVE SEX RATIO ADJUSTMENT IN THE POLLINATING FIG WASP PLATYSCAPA AWEKEI

Female hymenoptera are renowned for their ability to adjust offspring sex ratio to local mate competition. When two females share a patch, they frequently produce clutches that differ in size, the female with the larger clutch optimally producing a more female‐biased sex ratio and vice versa. Females can base their sex allocation on their own clutch size only (“self‐knowledge”) or on both females’ clutch sizes (“complete knowledge”). Few studies have genotyped offspring so that each mother's contribution can be considered separately while none has found that both sources of information are used simultaneously. We genotyped 2489 wasps from 28 figs and assigned their maternity to one of the two foundress females. We argue that likelihood is a very convenient method to compare alternative models, while fitness calculations help to appreciate the cost of maladaptation. We find that the pollinating fig wasp Platyscapa awekei simultaneously uses its own as well as the other females clutch size in allocating sex. Indeed, the complete knowledge model explains the data 36 times better than the self‐knowledge model. However, large clutches contained fewer males than the optimal predictions leading to a median selection coefficient of 0.01.     

Factors affecting the reproductive biology of Melittobia digitata and failure to meet the sex ratio predictions of Hamilton's local mate competition theory

Melittobia digitata Dahms (Eulophidae, Tetrastichini), a species of parasitic wasp satisfying all of Hamilton's local mate competition requisites, does not exhibit the predicted change in sex ratio with increased foundress number. A multifactorial design was used to test how age, oviposition experience, feeding experience, mating, and foundress number affect host‐acceptance, number of offspring, and sex ratio of this species developing on honey bee pupae, Apis mellifera (L.) (Apidae, Apini). All factors significantly affected the time it took for oviposition to commence. Females oviposited soonest when they were 2 days old, mated, had previous feeding and oviposition experience, and were placed on hosts with multiple foundresses. Although the age difference between 2‐ and 5‐day‐old females is small, it significantly affected reproductive behavior. Age, mating, and foundress number were found to have an effect on sex ratio, however, the foundress effect was found to be a mathematical artifact of the limited host size. After correcting for this variable, females were found to have a constant sex ratio of approximately 0.05. Several 2‐way interactions between factors were revealed: age and experience, age and foundress number, age and mating, foundress number and experience, and foundress number and mating. One 3‐way interaction was found between age, mating, and foundress number. This study demonstrates that the sex ratio of M. digitata is not altered with increased foundresses, as predicted by Hamilton , and that slight changes in preconditioning may modify reproductive behavior.     

Postemergence Experience Affects Sex Ratio Allocation in a Gregarious Insect Parasitoid

We tested the hypotheses that postemergence experience with plants (“early adult learning”) modifies sex ratio and clutch size allocations of Cotesia congregata (Say) (Hymenoptera: Braconidae), a gregarious larval endoparasitoid of Manduca sexta L. (Lepidoptera: Sphingidae). Emerging wasps were exposed for 2–3 h to (a) one of two host plants (tomato or tobacco) or no plant, and (b) one of two novel plants (arugula or parsley) or no plant. Each female was permitted a single oviposition in a host offered with one of the two plant species 24 h later. Hosts were reared on laboratory diet before and after parasitization. Wasps exposed to either host plant allocated proportionately more females to hosts offered with the plant species experienced at emergence than wasps with the alternate species, but clutch sizes did not differ. Irrespective of plant species, wasps exposed to novel plants allocated proportionately more females to hosts than wasps without plant experience, and larger clutches to hosts offered with parsley than with arugula. Differential responses to host and novel plants suggest inherent recognition of host foodplants by C. congregata. Results demonstrate a direct effect of learning on reproductive potential.     

Egg load is a cue for offspring sex ratio adjustment in a fig‐pollinating wasp with male‐eggs‐first sex allocation

Fig‐pollinating wasps (Agaonidae) only reproduce within fig tree inflorescences (figs). Agaonid offspring sex ratios are usually female‐biased and often concur with local mate competition theory (LMC). LMC predicts less female‐bias when several foundresses reproduce in a fig due to reduced relatedness among intra‐sexually competing male offspring. Clutch size, the offspring produced by each foundress, is a strong predictor of agaonid sex ratios and correlates negatively with foundress number. However, clutch size variation can result from several processes including egg load (eggs within a foundress), competition among foundresses and oviposition site limitation, each of which can be used as a sex allocation cue. We introduced into individual Ficus racemosa figs single Ceratosolen fusciceps foundresses and allowed each to oviposit from zero to five hours thus variably reducing their eggs‐loads and then introduced each wasp individually into a second fig. Offspring sex ratio (proportion males) in second figs correlated negatively with clutch size, with males produced even in very small clutches. Ceratosolen fusciceps lay mainly male eggs first and then female eggs. Our results demonstrate that foundresses do not generally lay or attempt to lay a ‘fixed’ number of males, but do ‘reset to zero’ their sex allocation strategy on entering a second fig. With decreasing clutch size, gall failure increased, probably due to reduced pollen. We conclude that C. fusciceps foundresses can use their own egg loads as a cue to facultatively adjust their offspring sex ratios and that foundresses may also produce more ‘insurance’ males when they can predict increasing rates of offspring mortality.     

Putting your eggs in several baskets: oviposition in a wasp that walks between several figs

The interaction between figs (Ficus spp., Moraceae) and their pollinator fig wasps (Hymenoptera: Agaonidae) is an obligate mutualism, but females of dioecious fig trees exploit fig wasps without providing rewards. Figs are closed inflorescences that typically trap pollinator females after entry, but some fig wasp species can re‐emerge (although wingless) and subsequently oviposit in and pollinate further figs. Using glasshouse populations, we examined the sex ratios and clutches laid by single foundresses of Kradibia tentacularis (Grandi) in their first and subsequent male figs of Ficus montana Blume, and how the probability of emergence and entering a second fig varied between seasons. A maximum of four figs were entered by any one foundress. Wingless foundresses were able to locate and enter figs up to 60 cm from the first fig they entered, but the probability of entry declined sharply with distance from that fig. The foundresses that re‐emerged produced slightly higher adult offspring totals than those that failed to re‐emerge. Clutch sizes of a single foundress in its first fig equalled those in all the subsequent figs combined, with clutch size per fig decreasing when more figs were entered. Smaller clutches had less female‐biased sex ratios. Figs were more numerous in summer than in winter, but the proportion of figs entered by only wingless foundresses remained unchanged. Movement between figs increases pollinator reproductive success in male figs, thereby encouraging foundresses that encounter a female tree to also move between and pollinate several female figs.     

Molecular markers reveal reproductive strategies of non‐pollinating fig wasps

1. Fig wasps have proved extremely useful study organisms for testing how reproductive decisions evolve in response to population structure. In particular, they provide textbook examples of how natural selection can favour female‐biased offspring sex ratios, lethal combat for mates and dimorphic mating strategies. 2. However, previous work has been challenged, because supposedly single species have been discovered to be a number of cryptic species. Consequently, new studies are required to determine population structure and reproductive decisions of individuals unambiguously assigned to species. 3. Microsatellites were used to determine species identity and reproductive patterns in three non‐pollinating Sycoscapter species associated with the same fig species. Foundress number was typically one to five and most figs contained more than one Sycoscapter species. Foundresses produced very small clutches of about one to four offspring, but one foundress may lay eggs in several figs. 4. Overall, the data were a poor match to theoretical predictions of solitary male clutches and gregarious clutches with n ? 1 females. However, sex ratios were male‐biased in solitary clutches and female‐biased in gregarious ones. 5. At the brood level (all wasps in a fig), a decrease in sex ratio with increasing brood size was only significant in one species, and sex ratio was unrelated to foundress number. In addition, figs with more foundresses contain more wasp offspring. 6. Finally, 10–22% of females developed in patches without males. As males are wingless, these females disperse unmated and are constrained to produce only sons from unfertilised eggs.     

Incubation capacity limits maximum clutch size in black-tailed gulls Larus crassirostris

Factors determining clutch size of birds have long been the central issue in studies in life histories. It is assumed that the configuration of brood patches could limit the maximum clutch size. To test this hypothesis we manipulated clutch sizes and measured egg temperature as well as reproductive consequences in black-tailed gulls Larus crassirostris , which usually lay two egg clutches and have three brood patches. Mean egg temperature in 4-egg clutches (32.6±1.0°C) was significantly lower than in 2-egg (34.6±0.4°C) and 3-egg clutches (34.1±0.4°C), because egg temperature of the coolest egg within a 4-egg clutch was often substantially lower than the other three eggs. The proportion of eggs hatching from 4-egg clutches (11.6%) was lower than those of 2-egg (49.1%) and 3-egg clutches (52.0%). Four-egg clutches had longer incubation periods (29.6±1.3 day) than 2-egg (28.1±1.7 day) and 3-egg clutches (28.0 ±1.3 day). The results indicate that incubation capacity, which may be determined by the configuration of brood patches, limits the maximum clutch size in black tailed gulls, but not the actual clutch size typically laid.     

Pollinating fig wasp Ceratosolen solmsi adjusts the offspring sex ratio to other foundresses

Abstract Local mate competition theory predicts that offspring sex ratio in pollinating fig wasps is female‐biased when there is only one foundress, and increased foundress density results in increased offspring sex ratio. Information of other foundresses and clutch size have been suggested to be the main proximate explanations for sex ratio adjustment under local mate competition. Our focus was to show the mechanism of sex ratio adjustment in a pollinating fig wasp, Ceratosolen solmsi Mayr, an obligate pollinator of the functionally dioecious fig, Ficus hispida Linn., with controlled experiments in the field. First, we obtained offspring from one pollinator and offspring at different oviposition sequences, and found that offspring sex ratio decreased with clutch size, and pollinators produced most of their male offspring at the start of bouts, followed by mostly females. Second, we found that offspring sex ratio increased with foundress density, and pollinators did adjust their offspring sex ratio to other females in the oviposition patches. We suggest that when oviposition sites are not limited, pollinators will mainly adjust their offspring sex ratio to other foundresses independent of clutch size changes, whereas adjusting clutch size may be used to adjust sex ratio when oviposition sites are limited.     

Patterns of sex ratio, virginity and developmental mortality in gregarious parasitoids

Theory considering sex ratio optima under ‘strict local mate competition with offspring groups produced by a single foundress’ makes a suite of predictions, one of which is a mean female bias. Treating individual offspring as discrete units, theory further predicts sex ratios to have low variance (precise sex ratio) and to equal the reciprocal of clutch size (one male per clutch). The maternal decision may be complicated by imperfect control of sex allocation, limited insemination capacity of sons and offspring developmental mortality: each can lead to virgin daughters (with zero fitness) and consequently select for less biased sex ratios. When clutches are small and/or developmental mortality is common, appreciable proportions of virgins are expected, even when control of sex allocation is perfect and the mating capacity of males is unlimited. This suite of predictions has been only partially tested. We provide further tests by examining sex ratios and developmental mortalities within and across species of locally mating parasitoids. We find a wide range of mean developmental mortalities (6–67%), but mortality distributions are consistendy overdispersed (have greater than binomial variance) and sexually differential mortality appears to be absent. Sex ratios are female biased and have low variance, but are not perfectly precise and variance is increased by mortality within species and (equivocally) across species. Sex ratios less biased than the reciprocal of clutch size are observed; probably due to a maternal response to developmental mortality in one species, and to limited insemination capacity in others. Cross species comparisons indicate that mean proportions of mortality and virginity are positively correlated. Virginity is more prevalent than predicted among species with higher mortalities but not among lower mortality species. Predicted relationships between virginity and clutch size are supported in species with lower mortalities but only partially supported when mortality rates are higher.     

Quantitative tests of sex ratio models in a pollinating fig wasp

Pollinating fig wasps are often used to study sex ratio evolution in structured mating populations. Theory predicts a female-biased sex ratio, becoming less female biased as female (foundress) density increases. We usedLiporrhopalum tentacularis to test two mechanisms of sex ratio control when foundresses oviposit simultaneously: (1) foundresses facultatively adjust the number of males in clutches, and (2) they produce the same number of males regardless of clutch size, which, given limited numbers of oviposition sites, would lead to increases in sex ratio with increasing density. We then examined whether foundresses can oviposit sequentially into figs. When oviposition was simultaneous, brood composition indicated facultative adjustment, although sex ratios were more female biased than predicted. Instead, foundresses appeared to adjust their sex ratio in response to both others ovipositing and their own fecundity. We also found that foundresses are able to oviposit completely sequentially, with those arriving second adjusting their sex ratio in response to the previous oviposition. Hence, pollinating wasps may fail to fit the predictions of classical sex ratio theory because the conditions under which foundresses oviposit, and their responses to changes in such conditions, are more complex than once assumed. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.     

Adaptive seasonal trend in brood sex ratio: test in two sister species with contrasting breeding systems

Evolutionary theory predicts adaptive adjustment in offspring sex ratio by females. Seasonal change in sex ratio is one possibility, tested here in two sister species, the Common sandpiper and the Spotted sandpiper Actitis hypoleucos and A. macularia. In the monogamous Common sandpiper, males are the most competitive sex. In each of 3 years, there was a change from mainly sons in early clutches to mainly daughters in late clutches. This seasonal adjustment of clutch sex ratio took place within the female before the eggs were laid, not by differential egg or chick survival. The sex of all eggs laid in the clutches used here was determined molecularly from chick blood taken at the time of hatching. The Spotted sandpiper in contrast is polyandrous, with partly reversed sex roles. There was no seasonal trend from sons to daughters in this species. When tested together, the two species differed significantly as predicted by the hypothesis of adaptive sex ratio adjustment by females.     

Effects of time-dependent competition for oviposition sites on clutch sizes and offspring sex ratios in a fig wasp

Fig wasps have been known as one of the best-documented examples of female-biased sex ratio predicted from the local mate competition (LMC) theory. However, observed sex ratios appear more female-biased than predicted. Before a close match between theory and observation can be claimed, the number and sex ratio of offspring left by each foundress in a multi-foundress syconium need to be determined. We examined the clutch size and sex ratio of individual females of the pollinator fig wasp Blastophaga nipponica (Agaonidae) in experiments using a pair of fertile and sterile females in which sequence and time interval of entering syconia were manipulated. To determine the number and sex ratio of offspring left by each foundress in a multi-foundress syconium, we prepared sterilized females that could oviposit ordinarily but whose offspring could not develop at all, by irradiating the females with ⁶⁰Co gamma rays. Female fig wasps contributed different numbers and sex ratios of offspring to the total brood within a syconium, due to different entry times among them. The variation in clutch sizes with different entry times appeared to be caused by competition for oviposition sites, and sex ratios to be adjusted according to the clutch size.     

Pre-ovulation control of hatchling sex ratio in the Seychelles warbler

Females of some bird species have a high degree of control over the sex ratio of their offspring at laying. Although several mechanisms have been put forward to explain how females might control the sex of their eggs, virtually nothing is known. As females are the heterogametic sex in birds, adjustment of the clutch sex ratio could arise either by pre- or post-ovulation control mechanisms. The Seychelles warbler (Acrocephalus sechellensis) exhibits extreme adaptive egg sex ratio bias. Typically, warblers produce only single-egg clutches, but by translocating pairs to vacant habitat of very high quality, most females were induced to produce two-egg clutches. Overall, females skewed clutch sex ratios strongly towards daughters (86.6%). This bias was evident in the first egg, but critically, also in the second eggs laid a day apart, even when all absent, unhatched, or unsexed second eggs were assumed to be male. Although a bias in the first egg may arise through either pre- or post-ovulation mechanisms, the skew observed in second eggs could only arise through pre-ovulation control. Post-ovulation adjustment may also contribute to skewed hatchling sex ratios, but as sex-biased release of gametes is likely to be a more efficient process of control, pre-ovulation mechanisms may be the sole means of adjustment in this species. High fitness differentials between sons and daughters, as apparent in the Seychelles warblers, may be necessary for primary sex ratio adjustment to evolve.     

Genetic structure of natural Nasonia vitripennis populations: validating assumptions of sex-ratio theory

The parasitic wasp Nasonia vitripennis has been used extensively in sex allocation research. Although laboratory experiments have largely confirmed predictions of local mate competition (LMC) theory, the underlying assumptions of LMC models have hardly been explored in nature. We genotyped over 3500 individuals from two distant locations (in the Netherlands and Germany) at four polymorphic microsatellite loci to validate key assumptions of LMC theory, in terms of both the original models and more recent extensions to them. We estimated the number of females contributing eggs to patches of hosts and the clutch sizes as well as sex ratios produced by individual foundresses. In addition, we evaluated the level of inbreeding and population differentiation. Foundress numbers ranged from 1 to 7 (average 3.0 ± 0.46 SE). Foundresses were randomly distributed across the patches and across hosts within patches, with few parasitizing more than one patch. Of the hosts, 40% were parasitized by more than one foundress. Clutch sizes of individual foundresses (average 9.99 ± 0.51 SE) varied considerably between hosts. The time period during which offspring continued to emerge from a patch or host correlated strongly with foundress number, indicating that sequential rather than simultaneous parasitism is the more common. Genetic differentiation at the regional level between Germany and the Netherlands, as estimated by Slatkin's private allele method (0.11) and Hedrick's corrected G' _LT (0.23), indicates significant substructuring between regions. The level of population inbreeding for the two localities ( F _IL = 0.168) fitted the expectation based on the average foundress number per patch.     

First report of Melittobia australica Girault in Europe and new record of M. acasta (Walker) for Italy

Melittobia acasta and Melittobia australica are newly recorded from Sicily, Italy, and the second species is reported in Europe for the first time. A short historical background about Melittobia parasitoid wasps, their hosts, and distribution, with emphasis in those two species is presented together with illustrations to facilitate their identification. Brief discussion about the presence and possible distribution of the species in Sicily is also included.