韭菜迟眼蕈蚊雄虫日龄对其交配能力和雌虫生殖力的影响

为了提高韭菜迟眼蕈蚊性信息素监控水平,本文在25℃、RH70%±5%、光周期L∶D=14∶10的条件下研究韭菜迟眼蕈蚊不同日龄雄虫的交配能力及其对雌虫生殖力的影响。结果表明,未交配雄虫平均寿命4.5d,雌虫4.2d,雌雄成虫的平均寿命无显著差异。雄虫一生最多可交配13次,且随着雄虫日龄增加,雌虫交配成功率逐渐减少。随着雄虫交配经历的增加,雌虫交配的时间延长,最长达97min。雄虫的日龄并不影响与之交配雌虫的产卵量和卵孵化率,但是雄虫的交配经历与雌虫的产卵量和卵孵化率相关,尤其当雄虫交配经历超过8次时,与之交配的雌虫的产卵量和卵孵化率显著下降。研究阐明了韭菜迟眼蕈蚊的生殖行为特征,为其性信息素应用提供了参考。     

蛾类雄虫交配史对雌虫生殖适合度的影响:Meta分析

本文利用Meta分析方法,从29篇实例研究性文献中对27种雌性蛾类的适合度参数(产卵量、孵化率和寿命)进行分析,以确定雄虫的交配史如何影响雌虫的生殖适合度以及这种影响是否受科属和交配策略的影响。结果表明:雄虫的交配史对自身的精包大小或精子数量以及雌虫的生殖适合度具有明显的负作用,且这种负作用明显受科属和交配策略的影响;在菜蛾科、草螟科、螟蛾科、潜蛾科和蓑蛾科中,与有交配经历的雄虫交配后,雌蛾产卵量明显下降,但在卷蛾科和夜蛾科中没有差异;在潜蛾科、蓑蛾科、卷蛾科和夜蛾科中,与有交配经历的雄虫交配后,雌蛾卵孵化率明显下降,但在菜蛾科、草螟科和螟蛾科中没有差异;草螟科和螟蛾科中的雌蛾寿命随雄蛾的交配史而缩短,而卷蛾科和夜蛾科的雌蛾寿命随配偶的交配史而明显增加;尽管雄蛾交配史对单配制和多配制雌蛾的产卵量和孵化率具有明显的负作用,但雄虫的交配史明显缩短了单配制雌蛾的寿命而延长了多配制雌蛾的寿命;因此我们认为,在蛾类昆虫中,雄虫的交配史是影响雌虫生殖适合度的关键因素之一。     

优雅蝈螽雌虫性选择

优雅蝈螽雌虫在交配过程中接受雄虫分泌的精包,并且在交配后一段时间内把精包吃掉。精包对雌虫的生殖是必需的,体重大的雄性分泌的精包较大。把2只鸣叫的且体重不同的雄虫放在一起,雌虫会选择体重大的个体交配。     

樟叶蜂两性生殖与孤雌生殖方式下雌虫生殖适合度及子代生活史特征的比较

【目的】樟叶蜂Mesoneura rufonota是危害樟树Cinnamonum campora的重要食叶性害虫,该虫的繁殖策略包括两性生殖和孤雌生殖两种模式。本研究旨在明确孤雌生殖在樟叶蜂生活史中的生物学意义。【方法】在室内25℃恒温条件下,测定并分析了樟叶蜂孤雌生殖和两性生殖两种生殖方式在亲代生殖适合度(雌虫寿命、产卵量和卵孵化率)和子代生活史(各虫态发育历期、死亡率、子代性比和产卵量等)特征上的差异。【结果】孤雌生殖的樟叶蜂雌虫寿命显著长于两性生殖的雌虫寿命,而雌虫产卵量和卵孵化率在两种生殖方式间均无差异。子代各虫态的发育历期和死亡率以及子代单雌产卵量在两种生殖方式间均无差异,但子代成虫性比在两种生殖方式间存在显著差异,表现为孤雌生殖大多产雄性子代,而两性生殖大多产雌性子代。【结论】樟叶蜂的孤雌生殖延长了亲代雌虫的寿命,且为产雄孤雌生殖。这些研究结果表明,樟叶蜂的孤雌生殖不但具有自身建群的能力,同时在种群繁衍中可以提供大量的雄虫以弥补两性生殖后代雄性个体的不足。     

樟叶峰两性生殖与孤雌生殖方式下雌虫生殖适合度及子代生活史特征的比较

【目的】樟叶蜂Mesoneura rufonota是危害樟树Cinnamonum campora的重要食叶性害虫,该虫的繁殖策略包括两性生殖和孤雌生殖两种模式。本研究旨在明确孤雌生殖在樟叶蜂生活史中的生物学意义。【方法】在室内25℃恒温条件下,测定并分析了樟叶蜂孤雌生殖和两性生殖两种生殖方式在亲代生殖适合度(雌虫寿命、产卵量和卵孵化率)和子代生活史(各虫态发育历期、死亡率、子代性比和产卵量等)特征上的差异。【结果】孤雌生殖的樟叶蜂雌虫寿命显著长于两性生殖的雌虫寿命,而雌虫产卵量和卵孵化率在两种生殖方式间均无差异。子代各虫态的发育历期和死亡率以及子代单雌产卵量在两种生殖方式间均无差异,但子代成虫性比在两种生殖方式间存在显著差异,表现为孤雌生殖大多产雄性子代,而两性生殖大多产雌性子代。【结论】樟叶蜂的孤雌生殖延长了亲代雌虫的寿命,且为产雄孤雌生殖。这些研究结果表明,樟叶蜂的孤雌生殖不但具有自身建群的能力,同时在种群繁衍中可以提供大量的雄虫以弥补两性生殖后代雄性个体的不足。     

胸窗萤的生殖习性

研究胸窗萤Pyrocoelia pectoralis Olivier雌、雄成虫生殖系统、交配和产卵行为。描述雌雄成虫在求偶过程中的多种行为:寻找、竞争、抱对、交配、受精。雌雄交配时间可持续(82.5±34.8)min(n=15),雌雄均有多次交配现象。雌虫羽化后可立即交配产卵。在(25±2)℃室温下,雌虫寿命8.87±2.06d(n=30),雌萤平均产卵量为72.03±34.38粒(n=30),产卵量与雌虫体重呈正相关关系(y=235.28x-20.38,R2=0.7283,df=43,P<0.01);而产卵日龄与每日产出率呈指数函数关系(y=1.5339e-0.9148x,R2=0.9987,df=5,P<0.01)。因子分析结果显示,影响雌虫生殖力的因子可以归为外部形态因子和内在生理因子。     

细纹豆芫菁交配与繁殖力的关系

将采自野外的细纹豆芫菁EpicautamannerhimiMkl的雌雄成虫各50头在室内进行人工随机配对,共发生75次交配,平均交配1.5次。雄虫1生可交配0～4次,雌虫0～2次。交配持续时间为(188±55)min,交配持续时间与交配次数之间、交配持续时间与繁殖力之间均无相关性。交配次数与两性的繁殖力呈负相关。交配后有36头雌虫43次产卵,其中有35次产卵发生在本次交配后,有8次产卵发生在连续2次交配后。作者认为雌虫在性感受性上的差异,与不育雄虫参与雌虫的前次交配有关。雄虫能否产生足够数量的交配因子来抑制雌虫的性感受性,是决定雌虫在产卵前交配次数的重要因素。     

延迟交配对橘小实蝇繁殖适度的影响

橘小实蝇Bactrocera dorsalis Hendel是一种世界性的入侵害虫,严重为害多种经济果蔬。本文通过响应面分析方法,研究了延迟交配对橘小实蝇交配率、产卵量、孵化率和寿命的影响。结果表明,交配率随雌虫交配日龄的延迟先增后减,雌、雄成虫均为35日龄处理组中的交配率最高,为81.00%±2.00%;而雄虫交配日龄的延迟则对其卵孵化率有明显的负面作用,在56日龄雄虫与35日龄雌虫处理组中,其卵孵化率最低,仅为27.56%±4.55%。雌成虫产卵量和寿命受到雌、雄虫双方交配日龄的的影响,产卵量（y）与雄虫日龄（x1）和雌虫日龄（x2）的回归方程为y=514.36+3.08x1-11.05x2,雌成虫寿命（y）与雄虫日龄（x1）和雌虫日龄（x2）的回归方程为y=35.85+0.23x1+0.40x2。研究结果为田间使用性信息素迷向法防治橘小实蝇提供了理论依据。     

同时而非先后一雌多雄交配增加不同温度下食蚜瓢虫的适合度（英文）

【目的】尽管一雌多雄在瓢虫科中常见,但各研究中获得的数据不足以解释雌虫多次交配和一雌多雄的一般适应性意义或适合度后果。本研究以温度为胁迫因子,旨在评价一雌多雄的某些益处（如增加的适合度）是否可传递给后代。【方法】本研究检测了黄斑盘瓢虫Coelophora saucia (Mulsant) 3种交配处理中的适合度：一雌一雄（与同一雄虫交配5次,1次/d）,先后一雌多雄（与5头不同的雄虫依次交配5次,即每天与新的雄虫交配1次）,以及同时一雌多雄（放进5头雄虫,任由雌虫选择雄虫,交配5次,1次/d）。观察了各交配处理不同温度下（25, 27和 30℃）繁殖力、卵的育性、后代发育和存活。【结果】结果表明,经历一雌多雄然后进行交配选择或竞争的雌性的繁殖能力最强,后代能在更广温度范围内最好地适应发育和存活。但先后一雌多雄交配的雌性与一雌一雄交配的雌性的繁殖能力相似。【结论】结果说明,在无交配选择或雄性竞争的条件下,一雌多雄的益处不明显。这可能是由于在依次射精的雄性间存在精子竞争,或由于雌性的隐性选择。据我们所知,本研究中观察发现的无交配选择时不表现一雌多雄的益处的现象,之前在昆虫中未观察到过。     

龟纹瓢虫对豆蚜的捕食功能反应及寻找效应研究

龟纹瓢虫雌虫和雄虫对豆蚜的功能反应符台Holling Ⅱ型模型,其模型为：Na=0．9233N／(1 0．0171N)(雌虫)和Na=0．8641N／(1 0．0164N)(雄虫),瓢虫捕食豆蚜的数量随豆蚜密度增加而增加．但寻找效应随豆蚜密度增加而降低。日最大捕食量和最佳寻找密度分别为37.42(雌)、34．11头(雄)和17．25（雌)、15．8头(雄)。龟纹瓢虫寻找效应随自身密度的增加而降低,其数学模型为：E=0．3032·P^-15634(雌)和E=0．3048·P^-1.1697(雄)。干扰反应的教学模型为：E=0．8104·P^-2.1721(雌),E=0．7125·P^-2.2660,E=0．5963·P^-2.1751(雌雄混台种群)。     

Heteropopulation males have a fertilization advantage during sperm competition in the yellow dung fly (Scathophaga stercoraria)

Sexual conflict occurs whenever there is not strict genetic monogamy. The sexually antagonistic coevolution that potentially occurs because of this conflict involves adaptation by one sex followed by the counter-adaptation by the other, and may be thought of as an evolutionary arms-race. As a result of these cycles of antagonistic coevolution, females from one population may be less resistant to heteropopulation males, at least after short periods of allopatry, as they will not have evolved any resistance to them. We tested this prediction in yellow dung fly (Scathophaga stercoraria) populations from the UK and Switzerland. Males from each population mated as first and second males to females from each population, and the mean numbers of offspring sired by the last male to mate in each situation were compared. We also compared the fertility and fecundity of single females mated to males from both populations, as well as the fertility and fecundity of the F(1) crosses. Both crosses produced viable and fertile offspring and the offspring sex ratios were not skewed. However, the fecundity of F(1)-cross females was greater than that of the parentals. In the sperm-competition experiment, there was a significant interaction between male and female origin influencing the proportion of offspring sired by the second male to mate, with heteropopulation males always outcompeting conpopulation males. This effect was independent of copula duration and the delay between copulations. In a separate experiment, we tested to see whether this was due to female preference for genetically dissimilar males but found no evidence for paternity biasing based on genetic similarity. Our results therefore seem to be best explained by sexually antagonistic coevolution as females appear less resistant to males with which they have not coevolved.     

Constrained sex allocation in a parasitoid due to variation in male quality

The theory of constrained sex allocation posits that when a fraction of females in a haplodiploid population go unmated and thus produce only male offspring, mated females will evolve to lay a female-biased sex ratio. I examined evidence for constrained sex ratio evolution in the parasitic hymenopteran Uscana semifumipennis. Mated females in the laboratory produced more female-biased sex ratios than the sex ratio of adults hatching from field-collected eggs, consistent with constrained sex allocation theory. However, the male with whom a female mated affected her offspring sex ratio, even when sperm was successfully transferred, suggesting that constrained sex ratios can occur even in populations where all females succeed in mating. A positive relationship between sex ratio and fecundity indicates that females may become sperm-limited. Variation among males occurred even at low fecundity, however, suggesting that other factors may also be involved. Further, a quantitative genetic experiment found significant additive genetic variance in the population for the sex ratio of offspring produced by females. This has only rarely been demonstrated in a natural population of parasitoids, but is a necessary condition for sex ratio evolution. Finally, matings with larger males produced more female-biased offspring sex-ratios, suggesting positive selection on male size. Because the great majority of parasitic hymenoptera are monandrous, the finding of natural variation among males in their capacity to fertilize offspring, even after mating successfully, suggests that females may often be constrained in the sex allocation by inadequate number or quality of sperm transferred.     

Production and export of the parasitoid Tachardiaephagus somervilli (Chalcidoidea: Encyrtidae), a biological control agent for the yellow lac scale,Tachardina aurantiaca (Hemiptera: Coccoidea: Kerriidae)

Development and reproduction of the hymenopteran parasitoid Tachardiaephagus somervilli Mahdihassan (Chalcidoidea: Encyrtidae) were studied in its native range in Malaysia as part of a classical biological control program on Christmas Island (Indian Ocean). Tachardiaephagus somervilli was reared in the laboratory on its target host, the yellow lac scale, Tachardina aurantiaca Cockerell (Coccoidea: Kerriidae). The developmental time, survival, and sex ratio of F1 offspring from two different sources of F0 adults (field-collected F0 adults [=‘wild-caught’] and F0 adults that emerged from parasitized hosts in the laboratory [=‘laboratory-emerged’]) were compared. Sources of F0 adults did not affect the developmental time of either male or female offspring, which ranged from 23 to 25 days. Furthermore, per capita fecundity of laboratory-emerged F0 females was three times greater than wild-caught F0 females. The number of emerged F1 adults was positively related to host size. Tachardiaephagus somervilli has a short generation time relative to its female Tachardina hosts (~23 vs ~90 days), high fecundity (~16 emerged offspring per laboratory-emerged female) and can potentially complete 12–15 generations per year. This rearing protocol produced sufficient quantities of adult T. somervilli for the export and successful introduction to Christmas Island (Indian Ocean) for the biological control of invasive T. aurantiaca, with near 100% survival rates for both sexes during transit.     

Radiation biology and inherited sterility in false codling moth (Lepidoptera: Tortricidae)

False codling moth, Cryptophlebia leucotreta (Meyrick), male and female mature pupae and newly emerged adults were treated with increasing doses of gamma radiation and either inbred or out-crossed with fertile counterparts. For newly emerged adults, there was no significant relationship between dose of radiation and insect fecundity when untreated females were mated to treated males (N female by T male). However, fecundity of treated females mated to either untreated (T female by N male) or treated males (T female by T male) declined as the dose of radiation increased. A similar trend was observed when mature pupae were treated. The dose at which 100% sterility was achieved in treated females mated to untreated males (T female by N male) for both adults and pupae was 200 Gy. In contrast, newly emerged adult males treated with 350 Gy still had a residual fertility of 5.2% when mated to untreated females, and newly emerged adult males that were treated as pupae had a residual fertility of 3.3%. Inherited effects resulting from irradiation of parental (P1) males with selected doses of radiation were recorded for the F1 generation. Decreased F1 fecundity and fertility, increased F1 mortality during development, and a significant shift in the F1 sex ratio in favor of males was observed when increasing doses of radiation were applied to the P1 males.     

Sperm competition generates evolution of increased paternal investment in a sex role‐reversed seed beetle

When males provide females with resources at mating, they can become the limiting sex in reproduction, in extreme cases leading to the reversal of typical courtship roles. The evolution of male provisioning is thought to be driven by male reproductive competition and selection for female fecundity enhancement. We used experimental evolution under male‐ or female‐biased sex ratios and limited or unlimited food regimes to investigate the relative roles of these routes to male provisioning in a sex role‐reversed beetle, Megabruchidius tonkineus, where males provide females with nutritious ejaculates. Males evolving under male‐biased sex ratios transferred larger ejaculates than did males from female‐biased populations, demonstrating a sizeable role for reproductive competition in the evolution of male provisioning. Although larger ejaculates elevated female lifetime offspring production, we found little evidence of selection for larger ejaculates via fecundity enhancement: males evolving under resource‐limited and unlimited conditions did not differ in mean ejaculate size. Resource limitation did, however, affect the evolution of conditional ejaculate allocation. Our results suggest that the resource provisioning that underpins sex role reversal in this system is the result of male–male reproductive competition rather than of direct selection for males to enhance female fecundity.     

Male-Biased Sex Ratios in Offspring of Attractive Males in the Guppy

The attractiveness hypothesis predicts that females produce offspring with male-biased sex ratios when they mate with attractive males because their male offspring will inherit the paternal sexual attractiveness and may have high reproductive success. In this study, we examined the effect of the attractiveness of the male guppy Poecilia reticulata in terms of the conspicuousness of its orange spot patterns, important criteria affecting female choice in this species, on the offspring sex ratios. We found that food-manipulation treatment altered the conspicuousness of the orange spot patterns in a full-sibling male pair. When females were presented to these males, they showed a greater mate preference for males having brighter orange spots than for those having duller orange spots. Subsequently, half of the females were mated with the preferred males and the remaining females were mated with the less preferred males. When the females exhibited a greater preference for their mates, their offspring sex ratios were more male biased. These results appear to be consistent with the prediction of the attractiveness hypothesis. In the guppy, as male sexual attractiveness is heritable, the male-biased sex ratios of the broods of attractive males may be adaptive.     

Sex ratios of Spalangia endius (Hymenoptera: Pteromalidae), in relation to current theory

Abstract. 1. Spulungiu endius Walker is a solitary parasitoid of house fly puparia.
2. The sex and size of S.endius was not related to host size.
3. In the laboratory the mean sex ratio of all offspring of nine groups, each comprising twenty females, was consistently female-biased (x = 83.5%, range 79–87%). The sex ratio in the field was less female-biased and showed greater fluctuation (61–75%). This may be a consequence of females laying male eggs before mating, some females remaining unmated, possible shorter adult life expectancy in the field than in the laboratory, and, perhaps, the presence of conspecific females.
4. The sex ratio of offspring of individual females varied from 66% to 100% females, and males were deposited early in the oviposition sequence.
5. Although a large number of fly puparia died before adult flies or parasitoids emerged (64.5%; n = 5874), there was no differential mortality of either sex.
6. Our results fit no general sex ratio hypothesis and we conclude that (i) the genetic nature of sex ratios in these insects needs careful examination, and (ii) the prevalence of female-biased sex ratios in solitary parasitoids needs investigation.     

Female Control of Offspring Sex Ratios Based on Male Attractiveness in the Guppy

The sex allocation hypothesis predicts that females manipulate the offspring sex ratios according to mate attractiveness. Although there is increasing evidence to support this prediction, it is possible that paternal effects may often obscure the relationship between female control of offspring sex ratios and male attractiveness. In the present study, we examined whether females played a primary role in the manipulation their offspring sex ratios based on male attractiveness, in the guppy Poecilia reticulata, a live‐bearing fish. We excluded the paternal effects by controlling the relative sexual attractiveness of the male by presenting them to the females along with a more attractive or less attractive stimulus male. The test male was perceived to be relatively more attractive by females when it was presented along with a less attractive stimulus male, or vice versa. Subsequently, test male was mated in two different roles (relatively more and less attractive) with two females. If females were responsible for offspring sex ratio manipulation, the sex ratio of the brood would be altered on the basis of the relative attractiveness of the test male. On the other hand, if males play a primary role in offspring sex ratio manipulation, the sex ratios would not differ with the relative attractiveness of the test male. We found that females gave birth to more male‐biased broods when they mated with test males in the attractive role than when they mated with males in the less attractive role. This finding suggests that females are responsible for the manipulation of offspring sex ratios based on the attractiveness of their mates.     

Influence of body size on fecundity and sperm management in the parasitoid wasp Anisopteromalus calandrae

A large body size is considered to be advantageous to the reproductive success of females as a result of several factors, such as the allocation of more resources to reproduction and the efficient management of sperm transferred by males. In the present study, the effects of female body size, female mating status and additional food availability on fecundity and the offspring sex ratio are investigated in the parasitoid wasp Anisopteromalus calandrae Howard (Hymenoptera: Pteromalidae). Because of haplodiploid sex determination, females must fertilize eggs to produce female offspring but not to produce male offspring. As predicted, female fecundity and the number of female offspring are positively correlated with body size. However, although the volume of the spermatheca increases with female body size, the amount of sperm stored in the spermatheca is relatively constant, irrespective of body size. Consequently, larger females produce a greater proportion of male offspring, especially at the end of the oviposition sequence, suggesting that larger females that possess more resources for reproduction and produce a larger number of offspring are more likely to suffer sperm depletion. The results of the present study also show that mated females have an increased fecundity compared with virgin females, although the opportunity to feed on honey along with host feeding has no impact upon fecundity or the sex ratio.     

Offspring sex ratio and development are determined by copulation activity in Echinothrips americanus MORGAN 1913 (Thysanoptera: Thripidae)

The costs of parthenogenetic reproduction are more or less unknown in thrips. However, IPM strategies require an understanding of temporal and spatial life‐history variations and sex ratios. Hence, different circumstances with regard to mating and sperm storage, and their effects on the life history of the adults and progeny, were tested in Echinothrips americanus. Different conditions were investigated: (1) one female and one male with permanent access to each other, (2) one female and one male with limited access to each other, (3) one virgin male only, (4) one virgin female only and (5) two virgin females permanently associated. Mating or not mating has a significant effect on the longevity of females and males, and on female fecundity. As a result of tested condition (2), limited access has a positive effect on longevity of a male. On the other hand, permanent access (1) or no access to a female (3) leads to shorter longevity of a male. For a female with permanent access to a male (1), longevity and oviposition rate are reduced. In addition, test conditions of parents have a significant effect on developmental time of the offspring and their sex ratio. Compared to a female under condition (1), a female with limited access to a male (2) delivers offspring with a more male‐biased sex ratio, independent of the period of time after last male access. Concerning the time for development of the offspring, females under condition (2) and under condition (4) deliver an F1 generation with a shorter developmental time than those under condition (1). Therefore, E. americanus seems to have a feedback system, that is offspring in low male‐biased populations develop faster and generate an adapted sex ratio. Hence, the assumption of a lower infestation risk in arrhenotokous than in thelytokous parthenogenesis should be reconsidered.