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Female-biased Sex Ratio (female-biased + sex_ratio)
Selected AbstractsHost age and fitness-related traits in a koinobiont aphid parasitoidECOLOGICAL ENTOMOLOGY, Issue 4 2005H. Colinet Abstract., 1.,Trade-offs play a key role in species evolution and should be found in host,parasitoid interactions where the host quality may differ between host age categories. 2.,The braconid wasp, Aphidius ervi, is a solitary endoparasitoid that allows its aphid hosts to continue to feed and grow after parasitisation. The hypotheses that host age influences their quality and that female parasitoids exploit their hosts based on that quality were tested under laboratory conditions using no-choice tests. 3.,Aphidius ervi females accepted the aphid Myzus persicae for oviposition and their progeny developed successfully in all host ages. The fitness-related traits of parasitoids did not increase linearly with the host age in which they developed. Host quality was found to be optimal at intermediate host ages and the females preferred to parasitise these hosts. The shortest progeny development time and a more female-biased sex ratio were observed in hosts of intermediate age. 4.,This study suggests the existence of multiple interactive trade-offs occurring during host,parasitoid interactions according to host age related quality. [source] Does the diapause experience of bumblebee queens Bombus terrestris affect colony characteristics?ECOLOGICAL ENTOMOLOGY, Issue 1 2000M. Beekman Summary 1. Bumblebee colonies show much variation in the number of workers, drones, and queens produced. Because this variation prevails even when colonies are kept under identical conditions, it does not seem to be caused by extrinsic factors but rather by differences between founding queens. 2. The most likely factor that could cause differences between queens is diapause. Although colonies are raised under standardised conditions, the queens often experience diapause of different length. If there are costs associated with diapause that influence post-diapause reproduction, the diapause history of the queens could affect colony characteristics. 3. Here, several colony characteristics are compared: number of first and second brood workers; total number of workers, drones, and queens; energy spent on sexuals; sex ratio; rate of worker production; time to emergence of first reproductive; and colony lifetime. Colonies were used where the queens experienced a diapause treatment of 0 (nondiapause queens), 2, and 4 months. 4. Although no proof was found for the existence of costs associated with diapause, the colony characteristics of nondiapause queens were significantly different from those of diapause queens. Colonies of nondiapause queens produced the lowest number of workers but the highest number of young queens. 5. It is argued that these nondiapause colonies are more time-constrained than diapause colonies because nondiapause colonies produce two generations within the same season and should therefore be more efficient in producing sexual offspring. 6. Moreover, nondiapause colonies should rear a more female-biased sex ratio because they can be certain of the presence of males produced by other (diapause) colonies. [source] Reversibility of estrogenic sex changes in zebrafish (Danio Rerio),ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 8 2009Mia G. Larsen Abstract Development of male zebrafish (Danio rerio) courtship behavior was studied following estrogenic disruption of sexual differentiation. Sixty zebrafish were exposed at 28C to 5 ng/L (nominal concentration) of 17,-ethinylestradiol (EE2) from the egg stage until adulthood at four months of age, resulting in a female-biased sex ratio. Twenty-five EE2 -exposed phenotypic female zebrafish were subsequently held in clean water for eight months. During this period, eight phenotypic males developed. These phenotypic males demonstrated significant behavioral aberrations and a low fertilization rate compared to control males. [source] INTERSEXUAL COMPETITION AS AN EXPLANATION FOR SEX-RATIO AND DISPERSAL BIASES IN POLYGYNOUS SPECIESEVOLUTION, Issue 11 2004Henri Leturque Abstract In polygynous mammals, it is commonly observed that both sex ratios at birth and dispersal are male biased. This has been interpreted as resulting from low female dispersal causing high female local resource competition, which would select for male-biased sex ratios. However, a female-biased sex ratio can be selected despite lower female than male-biased dispersal. This will occur if the low female dispersal is close to the optimal dispersal rate, while the male dispersal is not close to the optimal dispersal rate. The actual outcome depends on the joint evolution of sex-biased dispersal and sex ratio. Earlier analyses of joint evolution imply that there will be no sex-ratio nor dispersal biases at the joint evolutionarily stable strategy, thus they do not explain the data. However, these earlier analyses assume no intersexual competition for resources. Here, we show that when males and females compete with each other for access to resources, male-biased dispersal will be associated with male-biased birth sex ratio, as is commonly observed. A trend toward male-biased birth sex ratios is also expected if there is intersexual local resource competition and if birth sex ratio is constrained so that it cannot depart from balanced sex ratio. [source] Geographic variation in diapause induction and mode of diapause inheritance in Tetranychus pueraricolaJOURNAL OF APPLIED ENTOMOLOGY, Issue 5 2006Akiyuki Suwa Abstract:, Diapause induction and photoperiodic response curves were determined for 33 strains of Tetranychus pueraricola derived from kudzu vine at three constant temperatures (15, 18 and 20°C) under a short-day condition (10 : 14 h; light : dark). Females of all but one of the strains entered diapause at all three temperatures with little variation in diapause percentages among the strains. The exception was the southernmost strain, which was found to be a non-diapause (ND) strain. The critical photoperiod gradually decreased towards the south at a rate of about 1 h for each 5 degrees of latitude. The diapause strains (D1 and D2) exhibited 100% diapause, whereas the ND strain exhibited 0% diapause. By crossing these strains, we determined that ,non-diapause' was a dominant character over ,diapause' and the character was controlled by simple Mendelian inheritance. To clarify why the female progeny from the crosses between the D1 and ND strains did not segregate into the diapause and non-diapause phenotypes in a 1:1 ratio in the B1 generation, round-robin crosses were carried out among the three strains. The results showed that the F1 generation was reproductively compatible and showed high egg hatchability with a female-biased sex ratio. In the B1 generation, the crosses between the D1 and ND strains and between the D1 and D2 strains exhibited extremely low egg hatchability and produced mostly female progeny, whereas offspring from the crosses between the D2 and ND strains showed more than 50% hatchability for B1 eggs and a female-biased sex ratio. Thus, the absence of segregation observed in the crosses between the D1 and ND strains appears to be due to the severe hybrid breakdown that occurred in the B1 generation. [source] Nestling sex ratios in a population of Bluethroats Luscinia svecica inferred from AFLPÔ analysisJOURNAL OF AVIAN BIOLOGY, Issue 1 2000S. Questiau We studied the sex ratio of Bluethroat Luscinia svecica broods using AFLPs. Our aim was to test whether there is a bias towards males that could be explained by sexual selection theories, or conversely, a bias towards females that could help explain the female-biased sex ratio among juveniles observed at a wintering site. The AFLP technique was reliable in sexing the nestlings from even small initial DNA quantities. Given the large number of polymorphic markers that can be obtained for each primer combination, the probability of detecting a W-chromosome-linked fragment is reasonably high. As a consequence, this method could be used in other species for sex-ratio studies and for other genetic purposes. Among 246 nestlings, we found an overall proportion of males of 50.8% at hatching and the sex-ratio variation using broods as independent units was not significantly different from expectation under a binomial distribution. None of the parental and environmental variables tested changed significantly the deviance to the model. Thus, sex determination in the Bluethroat seems to match the classical Mendelian model of a 1:1 sex ratio and cannot explain the biased sex ratio towards juvenile females found at the wintering site. [source] Infrequent sporophyte production maintains a female-biased sex ratio in the unisexual clonal moss Hylocomium splendensJOURNAL OF ECOLOGY, Issue 5 2010Knut Rydgren Summary 1.,Sex ratios in unisexual bryophytes are most often female biased, whereas male-biased sex ratios predominate in unisexual seed plants. This ,bryophyte paradox', i.e. that sex ratios are biased in favour of the sex associated with the highest reproductive costs, has remained unexplained. 2.,Analysis of sex-ratio patterns via the influence of sex distribution on population growth rates (,) has not previously been carried out for bryophytes. We used this method to model how variation in sex ratio and sporophyte frequency influences , in the clonal bryophyte Hylocomium splendens. We obtained , by matrix modelling of synthetic experimental populations derived from demographic field data, using a linear two-sex model. 3.,In our set of experimental populations , varied between 1.13 and 1.27 in response to variation in sex ratio and sporophyte frequency, with the highest , obtained for the combination of a very low sporophyte frequency and a slightly female-biased sex ratio. 4.,Our results explain the female-biased sex ratio of H. splendens by the slightly lower survival of and production of vegetative offspring by males than by non-sporophytic females. 5.,Synthesis. According to our models, female dominance is the predicted outcome of low to moderate fertilization success and male performance intermediate between that of sporophytic and of non-sporophytic females. Our results therefore explain how a female-biased sex ratio can be maintained despite higher costs of reproduction in females than in males. In dioecious bryophytes, males and females must grow in close contact for fertilization to take place. Better performance of male ramets than of the female ramets they fertilize also explains how male clones can expand into female clones. A similar performance hierarchy of males and females may occur in unisexual clonal seed plants, but more efficient fertilization systems by pollination prevents the selective advantage of unfertilized females from being realized. This explains why vascular plant populations tend to be male biased. We hypothesise difference in fertilization distance range between sperm and pollen as a simple explanation why ramet level sex ratios are in general male dominated in clonal seed plants and female dominated in clonal bryophytes. [source] Can the extremely female-biased sex ratio of the social spider mites be explained by Hamilton's local mate competition model?ECOLOGICAL ENTOMOLOGY, Issue 6 2007YUKIE SATO Abstract 1.,Extremely female-biased sex ratios are known in the social spider mite species, Stigmaeopsis longus and S. miscanthi. Whether Hamilton's local mate competition (LMC) theory can explain such sex ratios was investigated. 2.,Significant changes of the progeny sex ratios in the direction predicted by the LMC model were found in both species when the foundress number changed. Therefore, LMC can partly explain the skewed sex ratios in these species. 3.,When the foundress number increased, the progeny sex ratio was still female biased and significantly different from the prediction of the LMC model for haplodiploidy. Relatedness between foundresses could not fully explain the female-biased sex ratios. Therefore, these results suggest that there are factors other than LMC skewing the sex ratios of these species toward female. [source] SOCIALITY IN THERIDIID SPIDERS: REPEATED ORIGINS OF AN EVOLUTIONARY DEAD ENDEVOLUTION, Issue 11 2006Ingi Agnarsson Abstract Evolutionary ,dead ends' result from traits that are selectively advantageous in the short term but ultimately result in lowered diversification rates of lineages. In spiders, 23 species scattered across eight families share a social system in which individuals live in colonies and cooperate in nest maintenance, prey capture, and brood care. Most of these species are inbred and have highly female-biased sex ratios. Here we show that in Theridiidae this social system originated eight to nine times independently among 11 to 12 species for a remarkable 18 to 19 origins across spiders. In Theridiidae, the origins cluster significantly in one clade marked by a possible preadaptation: extended maternal care. In most derivations, sociality is limited to isolated species: social species are sister to social species only thrice. To examine whether sociality in spiders represents an evolutionary dead end, we develop a test that compares the observed phylogenetic isolation of social species to the simulated evolution of social and non-social clades under equal diversification rates, and find that sociality in Theridiidae is significantly isolated. Because social clades are not in general smaller than their nonsocial sister clades, the spindly phylogenetic pattern,many tiny replicate social clades,may be explained by extinction rapid enough that a nonsocial sister group does not have time to diversify while the social lineage remains extant. In this case, this repeated origin and extinction of sociality suggests a conflict between the short-term benefits and long-term costs of inbred sociality. Although benefits of group living may initially outweigh costs of inbreeding (hence the replicate origins), in the long run the subdivision of the populations in relatively small and highly inbred colony lineages may result in higher extinction, thus an evolutionary dead end. [source] | ||||||||||