Sex chromosomes and origin of males and sex mosaics of the parthenogenetic stick insect Carausius morosus Br.

The chromosome complements of sporadic males and masculinized females of the thelytokous phasmid Carausius morosus Br. could be analysed in spermatogonia and ovarian follicle cells. Masculinized females with ovaries, ovotestes or testes have the female chromosome number, i.e., 61 autosomes and three sex chromosomes. The sex chromosomes, one being longer than the other two, are metacentric. In one masculinized female with testes the three sex chromosomes were different, apparently through a reciprocal translocation. The masculinized females are considered to be intersexes (phenotypic sex determination). The chromosome complement of males differs from that of females by lacking either one of the sex chromosomes or only a segment of one of these chromosomes (genotypic sex determination). The deleted sex chromosomes appear as acrocentrics and may have arisen through a chiasma between a translocated segment in one sex chromosome and its untransposed homologous region in another sex chromosome. One apparently telocentric sex chromosome may have originated from centric fission together with loss of the other arm. The sex chromosomes are positively heteropycntoic in the psermatogonia, also in those of masculinized females. En bloc heterochromatinization of the sex chromosomes, which seems to be under the direct or indirect control of one or more sites on the sex chromosomes themselves, functions in sex determination. The sex determination does not give a decisive answer to the question whether di-, tri-, or tetraploidy is involved.     

Genetic Variation for Sex Ratio Traits within a Natural Population of a Parasitic Wasp, Nasonia Vitripennis

By analyzing isofemale strains extracted from a natural population of Nasonia vitripennis, we detected variation for the sex ratios produced in fresh hosts (first sex ratios) and in previously parasitized hosts (second sex ratios). Under simple assumptions of population structure, this between-strain heterogeneity of first sex ratios results in heterogeneity of fitnesses. There is approximately ten percent difference in average fitnesses between the strains. (The fitnesses of second sex ratios are analyzed in the accompanying paper.) Average first and average second sex ratios are uncorrelated. There is significant between-female heterogeneity within some strains for first sex ratios but not for second sex ratios. In addition, the average direct-developing and diapause first sex ratios (but not second sex ratios) are significantly correlated. There are significant correlations between the direct-developing and diapause sex ratios produced by the same female. The strains differ in their effects on the sex ratio and size of another female's brood in the same host. Data on these types of variation for sex ratio traits are essential for further progress in the study of sex ratio evolution.     

Gametocyte sex ratio of a malaria parasite: experimental test of heritability

The gametocyte sex ratio of Plasmodium mexicanum, a malaria parasite of western fence lizards, was studied in a modified garden experiment. Each of 6 naturally infected lizards was used to initiate 20 replicate-infections in naive western fence lizards. A significant donor effect was observed for the sex ratios of recipient infections at their maximal parasitemia, and this effect was associated with the sex ratio of the donor infection. In 20 infections in which sex ratio was followed during the course of the infection, 9 revealed constant sex ratios and 11 showed an increase in proportion of males over time. Recipient sex ratio was correlated with another life-history trait, a composite of rate of asexual replication and peak parasitemia, such that higher Rate-Peak scores were associated with infections with less female-biased sex ratios. These results are placed into the context of sex ratio theory that concludes that the degree of selfing of parasite genotypes (number of parasite clones) within the vector will influence the evolution of gametocyte sex ratio. The theory predicts that the sex ratio should be under some genetic control and thus be heritable as observed in the experiment. Clonal diversity should also influence the life-history trait, Rate-Peak, which was found to be correlated with sex ratio.     

The effects of sex preselection on the sex ratio of families

Advances in the potential for couples to predetermine the sex of their children will have significant consequences for many aspects of society. Among the likely demographic impacts are changes in both population size and the sex ratio. The aim of this article is to assess the effects of sex preselection on the sex ratio of families. The expected family sex ratio is derived and characterized for couples with particular preferences for the sex composition of their families. When couples desire k children of one sex and none of the other, the proportion of children in the completed family that are of the desired sex falls with increasing k. Constraints on total family size further reduce this proportion. When couples have a desire for a balanced composition of one boy and one girl, and when they have a preference for, say, a boy to be born first, they can expect a proportion of boys in the family that at first rises, and then falls, as sex preselection methods improve.     

桃园中食心虫单一性诱芯及其复合配置的诱蛾效率比较

【目的】明确两种食心虫性诱芯复合配置的诱蛾效果,提高其监测或防治效率及其绿色环保化水平,为果树生产中食心虫的高效监测和绿色防控提供科学依据。【方法】田间系统调查研究了梨小食心虫(以下简称"梨小")、桃小食心虫(以下简称"桃小")单一性诱芯及其复合配置3种处理的诱蛾效率,并利用"Y"型嗅觉仪比较研究了其间梨小雄蛾趋向性的差异。【结果】(1)梨小和桃小性单一诱芯及其复合配置对梨小均具有引诱作用,其诱蛾总量依次为8 238.33、1 451.67、8 321.67头/诱捕器,其中第1、2、3代时复合配置诱蛾量最大,越冬代和第4代时梨小单一性诱芯诱蛾量最大,而各世代桃小单一性诱芯诱蛾量均最低。梨小单一性诱芯及其复合配置均监测到5个梨小发生高峰,且峰期基本一致,但复合配置的峰日诱蛾量均较高;桃小单一性诱芯仅监测到3个梨小发生高峰,且峰日诱蛾量亦较低。(2)桃小单一性诱芯及其复合配置对桃小均具有引诱作用,其诱蛾总量依次为4.00、2.33头/诱捕器,而梨小单一性诱芯对桃小无引诱作用。(3)"Y"型嗅觉仪研究发现,梨小食心虫对梨小和桃小各单一性诱芯及其复合配置均具有趋向作用,其趋向率依次为50.67%、8.67%、53.33%。【结论】梨小和桃小单一性诱芯复合配置对梨小诱捕量有微增效作用,而对桃小诱捕量有一定干扰作用,但影响均不显著。据此,该复合配置可用于桃园中梨小和桃小的监测与防控。     

The involvement of phytohormones in the plant sex regulation

The data concerning the plant sex regulation by phytohormones are presented. Functioning of signaling pathways regulating floral development and sex expression, including those with phytohormone involvement, are considered. The role of phytohormones in the functioning of systems and mechanisms of sex regulation is analyzed. The examples of sex reversion by plant treatment with phytohormones are presented. It is demonstrated that many genes determining sex encode proteins involved in the phytohormone metabolism. The significance of phytohormone investigation for the understanding of molecular mechanisms of plant sex regulation is discussed.     

The evolution of obligate sex: the roles of sexual selection and recombination

The evolution of sex is one of the greatest mysteries in evolutionary biology. An even greater mystery is the evolution of obligate sex, particularly when competing with facultative sex and not with complete asexuality. Here, we develop a stochastic simulation of an obligate allele invading a facultative population, where males are subject to sexual selection. We identify a range of parameters where sexual selection can contribute to the evolution of obligate sex: Especially when the cost of sex is low, mutation rate is high, and the facultative individuals do not reproduce sexually very often. The advantage of obligate sex becomes larger in the absence of recombination. Surprisingly, obligate sex can take over even when the population has a lower mean fitness as a result. We show that this is due to the high success of obligate males that can compensate the cost of sex.     

Genetic variation of sex allocation in the parasitoid wasp Heterospilus prosopidis

The genetic variation of sex ratio and sex allocation were examined in a series of half-sib analyses on the sex ratio of braconid parasitoid wasp Heterospilus prosopidis populations collected in Hawaii and Arizona. The mean threshold value and the range of the threshold for change in the sex of offspring in response to resource quality (host size) were determined. Estimates of the narrow-sense heritability (h2) of sex ratio at a specific host size ranged from 0.185 to 0.315, and those of the sex changing point (threshold value) ranged from 0.220 to 0.342. The coefficient of variation (CV(A)) of sex ratio was significantly larger than CV(A) of body weight. We discuss factors that maintained the significant additive genetic variation of sex ratio.     

Different origins of bird and reptile sex chromosomes inferred from comparative mapping of chicken Z-linked genes

Recent progress of chicken genome projects has revealed that bird ZW and mammalian XY sex chromosomes were derived from different autosomal pairs of the common ancestor; however, the evolutionary relationship between bird and reptilian sex chromosomes is still unclear. The Chinese soft-shelled turtle (Pelodiscus sinensis) exhibits genetic sex determination, but no distinguishable (heteromorphic) sex chromosomes have been identified. In order to investigate this further, we performed molecular cytogenetic analyses of this species, and thereby identified ZZ/ZW-type micro-sex chromosomes. In addition, we cloned reptile homologues of chicken Z-linked genes from three reptilian species, the Chinese soft-shelled turtle and the Japanese four-striped rat snake (Elaphe quadrivirgata), which have heteromorphic sex chromosomes, and the Siam crocodile (Crocodylus siamensis), which exhibits temperature-dependent sex determination and lacks sex chromosomes. We then mapped them to chromosomes of each species using FISH. The linkage of the genes has been highly conserved in all species: the chicken Z chromosome corresponded to the turtle chromosome 6q, snake chromosome 2p and crocodile chromosome 3. The order of the genes was identical among the three species. The absence of homology between the bird Z chromosome and the snake and turtle Z sex chromosomes suggests that the origin of the sex chromosomes and the causative genes of sex determination are different between birds and reptiles.     

The ultrastructure of the human sex vesicle

A correlated light and electron microscopical study has been made on the sex vesicle of human spermatocytes. The human sex vesicle contains no RNA and no ultrastructural granular element. The sex vesicle is formed at zygotene by the two heteropycnotic sex chromosomes that come into end-to-end contact at this stage. Neither the main nor secondary nucleoli are formed in connection with the human sex vesicle. The ultrastructure of the sex vesicle shows two main components: chromatin threads 250 of Å in diameter, separated by interthread spaces, and the filament or core, 700 Å wide and smoothly curved. No synaptinemal complexes have been observed in the human sex vesicle, although the filaments can become parallel for short segments. The absence of synaptinemal complexes is discussed in relation to the observations on other mammals.     

植物性别决定的研究进展

通过回顾近年来以多种植物为材料进行的性染色体观察,性别决定基因及调控方式的研究,对植物性别决定的机制进行了初步探讨,从而可以看出不同植物具有不同的性别决定机制：对于有性染色体的植物而言,目前已经从Y染色体上分离和鉴定了许多与雄性发育紧密相关的基因;部分性别决定基因和调控序列已利用构建减法文库,诱导突变体等方法从一些植物中获得。此外,还有研究表明,DNA脱甲基化,以及某些激素(如赤霉素、乙烯、Ace)都对植物的性别决定有重要作用。     

The end of gonad-centric sex determination in mammals

The 20th-century theory of mammalian sex determination states that the embryo is sexually indifferent until the differentiation of gonads, after which sex differences in phenotype are caused by the differential effects of gonadal hormones. However, this theory is inadequate because some sex differences precede differentiation of the gonads and/or are determined by non-gonadal effects of the sexual inequality in the number and type of sex chromosomes. In this article, I propose a general theory of sex determination, which recognizes multiple parallel primary sex-determining pathways initiated by genes or factors encoded by the sex chromosomes. The separate sex-specific pathways interact to synergize with or antagonize each other, enhancing or reducing sex differences in phenotype.     

Towards a genetic theory for the evolution of the sex ratio

A genetical model is formulated in which the sex ratio in broods and the relative size of broods are determined by the genotype at an autosomal locus. The results also apply to the case in which the sex-ratio locus is sex linked and expressed in the homogametic sex and to the case in which the locus is expressed in the diploid sex of a haplodiploid organism. Fisher (1930) argued that the sex ratio evolves under natural selection to a value such that parental expenditure is equalized between the sexes. Shaw and Mohler (1953) and MacArthur (1965) proposed that the sex ratio evolves to increase a certain expression for fitness. The sex ratio suggested by Fisher (1930) is in fact identical to the sex ratio specified by these maximization principles. Further, in our model, the Fisherian sex ratio corresponds exactly to the sex ratio at certain equilibria that are approached whenever they exist.     

黑斑蛙的减数分裂研究

本文研究了黑斑蛙的减数分裂,发现其性染色体所形成的性二价体主要呈末端与末端联接,浓缩期占79.6％,中期Ⅰ占75％,这进一步证明黑斑蛙确实存在XY型性别决定机制,这种XY型性染色体虽形态相同,但已发生了质的分化,可能是同型异质。黑斑蛙的性染色体并不形成性泡,少数二价体有中间交叉。     

Sex change in tree species: long-term monitoring of sex expression in Acer rufinerve

We monitored sex expression in Acer rufinerve from 1986 to 1999, in order to study branch-autonomous sex changes in tree species. During this observation period, 70 of 338 stems (20.7 %) changed sexual expression. Fifty of these sex-changed stems exhibited monoecism (having both female and male branches) in the course of the sex change, while the remaining stems changed directly from male to female or vice versa. A sex change resulting in monoecism was called a partial sex change and a total male/female change was referred to as a complete sex change. The mean diameter at breast height of stems that partially changed sex was significantly greater than that of stems that changed sex completely. Thus, it was primarily large stems with many branches that underwent partial sex changes. These findings suggest that sex change is a branch autonomous event in A. rufinerve and underline the importance of taking branching structure into account when studying sex change in trees.     

The many costs of sex

Explaining the evolution of sex is challenging for biologists. A 'twofold cost' compared with asexual reproduction is often quoted. If a cost of this magnitude exists, the benefits of sex must be large for it to have evolved and be maintained. Focusing on benefits can be misleading, as this sidelines important questions about the cost of sex: what is the source of the twofold cost: males, genome dilution or both? Does the cost deviate from twofold? What other factors make sex costly? How should the costs of sex be empirically measured? The total cost of sex and how it varies in different contexts must be known to determine the benefits needed to account for the origin and maintenance of sex.     

Current understanding of the development of sex attractant-based biocontrol in burnet moths

Burnet moths, also known as the family Zygaenidae, are a typical diurnal family of Lepidoptera. Some species are important insect pests in agriculture and forestry. The use of sex attractants is one of the most important measures in the integrated pest management of burnet moths because these attractants are highly efficient, do not cause pollution, and are convenient and harmless to natural enemies. The earliest information about sex pheromones in Zygaenidae was reported in 1972. To date, many studies have described sex pheromones and attractants of species in Zygaenidae. Here, we review a total of 22 sex attractant compositions identified for 57 species of Zygaenidae and compare the differences in the structures of sex attractants among these species. The application of sex attractants in seasonal monitoring showed that the main activity period of zygaenid moths is from May to September each year. However, there are few reports on the effects of sex attractants on mass trapping of members of the family Zygaenidae. The ratio and degradation of sex attractants and the trap color, shape and hanging height were considered the main factors influencing capture effectiveness. Directions for further study of burnet moths are also discussed.     

High elevation increases the risk of Y chromosome loss in Alpine skink populations with sex reversal

The view that has genotypic sex determination and environmental sex determination as mutually exclusive states in fishes and reptiles has been contradicted by the discovery that chromosomal sex and environmental influences can co-exist within the same species, hinting at a continuum of intermediate states. Systems where genes and the environment interact to determine sex present the opportunity for sex reversal to occur, where the phenotypic sex is the opposite of that predicted by their sex chromosome complement. The skink Bassiana duperreyi has XX/XY sex chromosomes with sex reversal of the XX genotype to a male phenotype, in laboratory experiments, and in field nests, in response to exposure to cold incubation temperatures. Here we studied the frequency of sex reversal in adult populations of B. duperreyi in response to climatic variation, using elevation as a surrogate for environmental temperatures. We demonstrate sex reversal in the wild for the first time in adults of a reptile species with XX/XY sex determination. The highest frequency of sex reversal occurred at the highest coolest elevation location, Mt Ginini (18.46%) and decreased in frequency to zero with decreasing elevation. We model the impact of this under Fisher’s frequency-dependent selection to show that, at the highest elevations, populations risk the loss of the Y chromosome and a transition to temperature-dependent sex determination. This study contributes to our understanding of the risks of extinction from climate change in species subject to sex reversal by temperature, and will provide focus for future research to test on-the-ground management strategies to mitigate the effects of climate in local populations.Subject terms: Evolutionary biology, Population genetics     

Spatial dynamics of adaptive sex ratios

According to Fisherian sex allocation theory, parents that can adjust their offspring sex ratio in response to skews in population sex ratio will maximize their fitness over parents lacking this ability. There is good evidence that adaptive sex ratio adjustment occurs in many natural populations, but deviations from theoretical predictions have also been observed. These anomalies may be more apparent than real. When the spatial dimension of sex ratio variation is ignored, then a mismatch between empirical data and theoretical predictions based on panmictic mating is to be expected. We illustrate this with data on human sex ratio variation in 21 preindustrial populations, and with a cellular automaton model built to obey Fisherian sex allocation rules. The results from the model generally match with the data. When information about the ambient sex ratio is limited, then the sex allocation decisions may appear locally maladaptive. In general, the results indicate that Fisher's sex-ratio theory may have greater explanatory power than previously thought.     

Behavior of gynandromorphs of the wasp Habrobracon juglandis.

A study was made of sex behavior for 276 gynandromorphs of the wasp Habrobracon juglandis. In general, gynandromorphs with male heads behaved like males, those with female heads behaved like females, and those with mosaic heads as either male or female or both. These observations corroborate those made by P. W. Whiting in 1932 and confirm his view that the site of sex behavior is in the brain. Correlations between sex behavior and the sex of various body structures showed clearly that sex behavior is unrelated to the thorax, abdomen and genitalia. The sex behavior of gynandromorphs does not seem to be related to the sex of the external sensors of the head but rather to the genotype of the brain.