The relationship of the demographic parameters of a population to its ecological niche constitutes one of the central problems of population biology. A most interesting theoretical notion pertinent to this problem is r- and K-selection (MacArthur 1962; Cody 1966; MacArthur and Wilson 1967; Hairston, Tinkle, and Wilbur 1970; Roughgarden 1971). The central idea of r- and K-selection is that populations living in environments imposing high density-independent (D.I.) mortality (r-strategists) will be selectively favored to allocate a greater proportion of resources to reproductive activities at the cost of their capabilities to propagate under crowded conditions, and conversely, populations living in environments imposing high density-dependent (D.D.) regulation (K-strategists) will be selectively favored to allocate a greater proportion of resources to nonreproductive activities, at the cost of their capabilities to propagate under conditions of high D.I. mortality. From the argument just stated, it may be deduced that the birth rate of an r-strategist will be greater than that of a related K-strategist. However, increased birth rate under conditions of high D.I. mortality is not sufficient evidence for an r-strategy, because, as demonstrated later in this paper, any increase in D.I. mortality must by itself produce a new equilibrium of birth and death rates at higher values of both. The crucial evidence needed for r- and K-selection is whether an organism is allocating a greater proportion of its resources to reproductive activities (r-strategists) than another related one (K-strategist) under any and all D.D. and D.I. mortality conditions.
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