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Precopulatory sexual selection is the association between fitness and traits associated with mate acquisition. Although sexual selection is generally recognized to be a powerful evolutionary force, most investigations are limited to characters belonging to individuals. A broader multilevel perspective acknowledges that individual fitness can be affected by aspects of mating success that are characters of groups, such as families. Parental mating success in polygynous or polyandrous human societies may exemplify traits under group-level sexual selection. Using fitness measures that account for age-structure, I measure multilevel selection for mate number over 55 years in a human population with declining rates of polygyny. Sexual selection had three components: individual-level selection for ever-mating (whether an individual mated) and individual- and family-level selection for polyandry and polygyny. Family- and individual-level selection for polygyny was equally strong, three times stronger than family-level selection for polyandry and more than an order of magnitude stronger than individual-level selection for polyandry. However, individual-level selection for polyandry and polygyny was more effective at explaining relative fitness variance than family-level selection. Selection for ever-mating was the most important source of sexual selection for fitness; variation for ever-mating explained 23% of relative fitness variance. [ABSTRACT FROM AUTHOR]

Bateman's classic paper on fly mating systems inspired quantitative study of sexual selection but also resulted in much debate and confusion. Here, I consider the meaning of Bateman's principles in the context of selection theory. Success in precopulatory sexual selection can be quantified as a “mating differential,” which is the covariance between trait values and relative mating success. The mating differential is converted into a selection differential by the Bateman gradient, which is the least squares regression of relative reproductive success on relative mating success. Hence, a complete understanding of precopulatory sexual selection requires knowledge of two equally important aspects of mating patterns: the mating differential, which requires a focus on mechanisms generating covariance between trait values and mating success, and the Bateman gradient, which requires knowledge of the genetic mating system. An upper limit on the magnitude of the selection differential on any sexually selected trait is given by the product of the standard deviation in relative mating success and the Bateman gradient. This latter view of the maximum selection differential provides a clearer focus on the important aspects of precopulatory sexual selection than other methods and therefore should be an important part of future studies of sexual selection. [ABSTRACT FROM AUTHOR]