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based on distinctions in replication strategies, is no less fundamental in that it contrasts the maximization of reproductive propagation (self-male) from that of the maximization of reproductive nurturance (other-female) Evolutionary biologists (Cole, 1954; Trivers, 1974; E O Wilson, 1975) have recorded marked differences among species in both the cycle and pattern of their reproductive behaviors Of special interest is the extreme diversity among and within species in the number of offspring spawned and the consequent nurturing and protective investment the parents make in the survival of their progeny Designated the r-strategy and K-strategy in population biology, the former represents a pattern of propagating a vast number of offspring but exhibiting minimal attention to their survival; the latter is typi ed by the production of few progeny followed by considerable effort to assure their survival.

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p = (p1 , p2 , , pm ) Let the random variable T denote the number of coin ips used in the algorithm We can describe the algorithm mapping strings of bits Z1 , Z2 , , to possible outcomes X by a binary tree The leaves of the tree are marked by output symbols X, and the path to the leaves is given by the sequence of bits produced by the fair coin For example, the tree for the distribution ( 1 , 1 , 1 ) is shown in Figure 57 2 4 4 The tree representing the algorithm must satisfy certain properties: 1 The tree should be complete (ie, every node is either a leaf or has two descendants in the tree) The tree may be in nite, as we will see in some examples 2.

Note: Most results of this subsection are given in Magnus (1988, 8). They follow from rules of the previous sections and the results for detf'tminants.

Exemplifying the r-strategy are oysters, which generate some 500 million eggs annually; the K-strategy is found among the great apes, which produce a single offspring every 5 to 6 years Not only do species differ in where they fall on the r- to K-strategy continuum, but within most animal species an important distinction may be drawn between male and female genders It is this latter differentiation that undergirds what has been termed the self- versus other-oriented polarity, implications of which are brie y elaborated in the following discussion Human females typically produce about four hundred eggs in a lifetime, of which no more than twenty to twenty ve can mature into healthy infants The energy investment expended in gestation, nurturing, and caring for each child, both before and during the years following birth, is extraordinary.

= the average call duration = Ph(1 BO)/[1 Phh(1 Pf )]

Not only is the female required to devote much of her energies to bring the fetus to full term, but during this period she cannot be fertilized again; in contrast, the male is free to mate with numerous females And should her child fail to survive, the waste in physical and emotional exertion not only is enormous, but also amounts to a substantial portion of the mother s lifetime reproductive potential There appears to be good reason, therefore, to encourage a protective and caring inclination on the part of the female, as evident in a sensitivity to cues of distress and a willingness to persist in attending to the needs and nurturing of her offspring Although the male discharges tens of millions of sperm on mating, this is but a small investment, given the ease and frequency with which he can repeat the act.