Abstract

Optimal allocation of parental resources is an important life history trait. However, it has been rarely investigated empirically. We tested aspects of optimal allocation theory in a digger wasp, the European beewolf. Investment allocation theory assumes (1) a trade-off between investment per offspring and offspring number and (2) a convex relationship between investment per offspring and fitness returns. From this relationship an optimum amount of investment per offspring can be derived and parents are predicted to provide each offspring with this optimum amount of investment. We used the number of bees in a brood cell as a measure of parental investment. Offspring fitness was quantified as both survival until emergence and success as adults. There is evidence for a trade-off between current and future reproduction, suggesting that the first assumption is met. In contradiction to the second assumption, one mortality factor, parasitism, increased proportionally with the number of bees in a brood cell. However, overall mortality until emergence significantly decreased with the number of bees in a brood cell as assumed by the theory. The determination of the optimum amount of investment per offspring is complicated because the sexes possibly differ in their relationship between amount of investment and fitness. Individual males received considerably fewer bees (2.2±0.8) than females (3.8±0.5). Two independent estimates of the investment specific survival suggested that sons with two bees had the highest fitness returns per single bee and, consistent with the prediction, most sons were provisioned with two bees. For daughters, four bees is probably the optimum amount and most daughters were provisioned with this number. In both sexes the variation of investment per offspring was less than expected by a Poisson distribution with the same mean. These findings support the view that parental investment is allocated in a way that optimizes the trade-off between offspring number and investment per offspring. However, variation contradicting the hypothesis still occurred. This might be explained either by adaptive variation in the amount of investment per offspring, constraints in the adjustment of the optimum amount of investment, or problems in measuring parental investment.

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