Abstracts (coauthor)

Why do spider mites re-mate?

Author(s): Rodrigues, L, Clemente S, Carvalho J, Duarte F, Ponce R, Varela S, Olivieri I, Magalhães S


In Tetranychus urticae, only the first mating is effective, except if the interval between first and second copulations is shorter than 24 hours or if the first mating is interrupted. However, males often attempt to copulate with mated females. Here, we address this paradox. We first tested whether males prefer to mate with females that have mated within the preceding 24 hours or with those that have mated before that period. We found that males show no preference between these two types of females. Moreover, the time to mating was longer and the mating duration shorter when males mated with mated females, relative to virgins, irrespective of their timing of mating. This confirms a lack of distinction between different types of mated females and suggests that males are either less motivated to mate with mated females or that the second mating occurs for a different reason than siring offspring. Subsequently, we investigated the consequences of polyandry for the reproductive fitness of females, depending on the frequency and timing of the mating events. We predicted that if females benefit from polyandry, fecundity and survival of multiply mated females would be higher than those of once mated females. Indeed, multiply mated females have higher fecundity than once mated females, suggesting that females potentially benefit from mating multiply. No difference in survival and sex ratio was found between these females. Our data shows that females benefit from multiple matings, hence this behaviour is probably under female control. This result has implications for our understanding of mating behaviour in spider mites and other organisms.


Observed differences between species are often due to differences at genomic level. In particular, the analysis of newly evolved genes provides information that helps us to understand the evolution of novel functions. Here, we examine the mechanisms involved in the formation of novel genes (less than 50 MYA) and we characterize the expression patterns of these genes. This illustrates the variety of mechanisms implicated in the formation of new genes, as well as the preferential location of expression of novel functions. We further analyze the Sdic gene family and use it to investigate in greater detail the formation and expression of novel genes. The Sdic gene family, a young gene family in Drosophila melanogaster, represents an interesting window into the evolution of novel genes, as it evolved after the split of D. melanogaster and D. simulans i.e. less than 2 million years ago. This gene family originated from a formation of a chimera of two unrelated genes, that was followed by several duplication events, being therefore a candidate for the study of two important mechanisms of gene formation: gene shuffling and duplication. This family is composed by several tandem copies of the gene Sdic, and at least one copy (sdic1) is expressed in testis, incorporated into the sperm tail and encodes a sperm specific intermediate chain. It has recently been showed that although this novel gene is not essential for the development of spermatids and Sdic knock-out males are fertile with no effect on the size or sex ratio of their progeny, Sdic has a role on sperm competition. This effect of Sdic in improving sperm competition suggests that Sdic may have had an important role, contributing to the species barrier between D. melanogaster and D. simulans. The analysis of particular newly evolved genes provides information in finer detail, that we hope can be generalized and will help understand the evolution of new genes and new functions in the genomes.


Chairman: Octávio S. Paulo
Tel: 00 351 217500614 direct
Tel: 00 351 217500000 ext22359
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email: mail@eseb2013.com


XIV Congress of the European Society for Evolutionary Biology

Organization Team
Department of Animal Biology (DBA)
Faculty of Sciences of the University of Lisbon
P-1749-016 Lisbon


Computational Biology & Population Genomics Group