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Does artificial selection on diapause incidence cause correlational changes in other life‐history traits? Case study in a spider mite population
Author(s) -
Ito Katsura
Publication year - 2009
Publication title -
entomologia experimentalis et applicata
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.765
H-Index - 83
eISSN - 1570-7458
pISSN - 0013-8703
DOI - 10.1111/j.1570-7458.2008.00819.x
Subject(s) - diapause , biology , spider mite , fecundity , heritability , population , tetranychus urticae , acari , life history theory , selection (genetic algorithm) , zoology , ecology , evolutionary biology , demography , life history , larva , artificial intelligence , sociology , computer science
Theoretical studies suggest that the timing of entering hibernation by arthropods has large effects on long‐term fitness, incurring strong selection pressure on diapause attributes every year. On the other hand, diapause attributes are often genetically correlated with other important life‐history traits such as fecundity or development time. To understand the evolutionary process of life cycle formation, there is a need to investigate not only diapause attributes themselves but also their genetic association with other life‐history traits. The Kanzawa spider mite, Tetranychus kanzawai Kishida (Acari: Tetranychidae), is a small herbivore that lives on the undersurface of host plant leaves. This mite has been investigated for the mode of inheritance of diapause attributes, but scarcely for genetic correlations with other life‐history traits. Here, I investigated whether diapause proneness, measured as the proportion of diapausing females under short‐day conditions, is genetically correlated with fecundity or development time under long‐day conditions using artificial selection experiments. Diapause incidence responded to the selection for both increasing and decreasing directions, suggesting that high genetic variance in diapause proneness is maintained in the study population. However, the change in proportion of diapausing females during the selection period was not associated with responses in fecundity or development time. These results suggest that diapause proneness and other life‐history traits have different genetic backgrounds, and thus diapause proneness may freely evolve without being constrained by changes in other life‐history traits.