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Sexual Offspring (sexual + offspring)
Selected AbstractsThe role of food and colony size in sexual offspring production in a social insect: an experimentECOLOGICAL ENTOMOLOGY, Issue 1 2007JOUNI SORVARI Abstract 1.,Large colonies of ants are known to have a higher propensity for sexual offspring production, probably owing to their high capacity to exploit food resources. 2.,The effects of food supplementation on the propensity for sexual offspring production, and whether it is linked with colony size, were investigated in an environment with poor resources (clear-cut areas). 3.,Large colony size was associated with a higher propensity for sexual offspring production in food-supplemented colonies, whereas in non-supplemented control colonies an association with colony size was not found. 4.,The results demonstrate that large colonies seem to have a higher capacity to exploit supplemented food. In addition, the production of sexual offspring was apparently limited by food availability in clear-cuts, especially for large colonies. [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] Production of asexual and sexual offspring in the triploid sexual planarian Dugesia ryukyuensisINTEGRATIVE ZOOLOGY (ELECTRONIC), Issue 3 2009Kazuya KOBAYASHI Abstract Certain freshwater planarians reproduce asexually as well as sexually, and their chromosomal ploidies include polyploidy, aneuploidy and mixoploidy. Previously, we successfully performed an experiment in which a clonal population produced by asexual reproduction of the Dugesia ryukyuensis (OH strain) switched to the sexual mode of reproduction. Worms of this strain are triploid with a pericentric inversion on Chromosome 4. The worms were switched to sexual reproduction after being fed with sexually mature Bdellocephala brunnea, which is a sexually reproducing species. The resulting sexualized OH strain produced cocoons filled with several eggs. Two putative factors, Mendelian factor(s) and chromosomal control(s), have been proposed as determining the reproductive mode. The present study demonstrated that inbreeding of the resultant sexualized worms produced the following four types of offspring through sexual reproduction: diploid asexual worms, triploid asexual worms, diploid sexual worms and triploid sexual worms. The chromosomal mutation on Chromosome 4 was inherited by these offspring independent of their reproductive mode. These results provide two important pieces of information: (i) the putative genetic factor was not necessarily inherited in a Mendelian fashion; and (ii) the reproductive mode is not regulated by chromosomal changes such as polyploidy or chromosomal mutations. This suggests that asexuality in D. ryukyuensis is regulated by an unknown factor(s) other than a Mendelian factor or a chromosomal control. [source] The founding mothers: the genetic structure of newly established Daphnia populationsOIKOS, Issue 5 2007Gerald Louette Colonization dynamics may strongly influence within and among population genetic variation and evolutionary potential of populations. We here analyze the genetic structure during the first three years of 12 cyclical parthenogenetic Daphnia populations in newly created pond habitats. One to three genotypes were observed to colonize the populations, indicating a limited number of founders. Pronounced changes in genetic structure were associated with hatching of sexual dormant eggs after a period of absence of the newly founded populations from the active community. Despite rapid colonization, genetic differentiation among populations was fairly high with limited decay over time, suggesting long-lasting founder effects. After initial colonization, no new alleles were observed in any of the populations, and our analyses suggests that this reflects reduced establishment success of later arrivals. Rare alleles increased in frequency, which likely is the result of inbreeding depression in selfed offspring of initially abundant clones, providing a fitness advantage to the sexual offspring of initially rare clones. [source] | ||||||||||