Introduction: Infanticide, Child Neglect, and the Concept of Parental Investment
Infanticide, either by a parent, by another relative, or by an unrelated individual of either sex is a widespread and very variable phenomenon in nature whose comprehension requires multiple explanatory frameworks. To date, the most widely reported form of infanticide among animals involves the killing of infants by unrelated males (e.g., in many species of nonhuman primates and cats and in certain strains of mice and lemmings) or by females with varying degrees of relatedness to the mother (e.g., species of ground squirrels and prairie dogs) (Hausfater and Hrdy, 1984; Hoogland, 1985). Although abandonment of infants or litters is not uncommon, animals in their natural habitats virtually never physically attack or directly destroy their own offspring. Humans, in this respect, are quite unusual among mammals in that across cultures parents themselves are the most likely perpetrators of infanticide through abandonment or even direct killing (these issues are discussed at length in Hausfater and Hrdy, 1984).
The decision to terminate further investment in a particular infant is typically made at birth or shortly after, and the mother is party to the decision (Dickemann, 1975; Minturn and Stashak, 1982; Daly and Wilson, 1984; Scrimshaw, 1984). Infanticide in such instances is probably usefully viewed as a very late form of abortion. From a sociobiological perspective, such parents are viewed as strategists whose ultimate goal is to increase the survival and lifetime breeding prospects of their entire lineage, even if it means a temporary setback in the form of a lost infant. It is assumed that each family has only limited resources to channel into reproduction. Since the time frame at issue is long term, a particular infant may be sacrificed if there is a chance that termination of investmentin a particular infant would, on average, eventually enhance opportunities to perpetuate the lineage. The classic example involves killing the youngest of two closely spaced children, withholding investment from a new infant in order to invest in a healthy, older child already past the perilous first years of life.
Theoretically then, family resources should be allocated according to the degree of relatedness of the parent or stepparent to the infant, how likely a candidate the offspring is for translating parental investment into subsequent reproduction (i.e., offspring quality), as well as according to what other options the parents have for using available resources (Alexander, 1974; Daly and Wilson, 1984 and Chapter 8, this volume). According to this perspective, parents perpetually monitor both the âworthâ of particular infants and their probable future demands on family resources (including demands long after weaning, such as marriage dowries), weighing these in the context of current socio-ecological conditions (e.g., anticipated investment from the father or other family members; family economic status; probable food availability) and invest in offspring accordingly (for an illustrative case study, see Bugos and McCarthy, 1984). Along the same lines, several authors have suggested that in some cases, offspring neglect in societies where infanticide is not an option may be a consequence of the same âdecision-makingâ process which reduces parental motivations to invest in a particular infant. Should this happen, additional demands for nurture made on the parent by the infant (or other parties) may result in abuse of the infant.
This conceptual framework derives from a particular model, a hypothetical continuum of parental investment beginning at conception and continuing through weaning and beyond where parents are (at some level) thought to be continuously monitoring the costs and benefits of additional investment. This model is both new and speculative but has already begun to attract attention from researchers in anthropology, biology, and public health (e.g., Hausfater and Hrdy, 1984). Even those subscribing to the model, however, differ in their assessment of how much of contemporary infanticide, and child abuse such a conceptual framework is likely to explain (compare, for example, Daly and Wilson, 1980 with Lenington, 1981). In my own opinion the model has the widest explanatory scope at low levels of subsistence (e.g., as among societies like the Ayoreo [Bugos and McCarthy, 1984]) and the narrowest in societies like our own which are (at least temporarily) characterized by a state of âecological release.â Starvation is uncommon, and parents virtually never benefit from killing an infant. In other words, I believe the model addresses itself to only a subset of contemporary western cases, a point dealt with elsewhere (Hrdy and Hausfater, 1984). The model remains relatively untested (see Daly and Wilson, Chapter 9 this volume, for an exception and for a slightly different perspective that stresses psychological motivations rather than outcomes), and the fact is we do not yet know to what extent child neglect and infanticide can be explained by such a model.
Cross-culturally, there appears to be little doubt that most cases of human infanticide seem directly related to parental perceptions of either offspring quality or of the probable quality of the subsistence base in the near future. However, in a small portion of cases, sex of the infant rather than quality per se turns out to be the significant variable. Sex preferential infanticide is uncommon but is reported to occur in nearly 9% of the worldâs cultures (Minturn and Stashak, 1982). In some extreme North Indian cases, all daughters born in certain groups are killed at birth, and wives for sons must be recruited from outside of the group (Miller, 1981; Dickemann, 1979).
Traditional preferences for sons in some Indian communities is currently manifested in parental decisions to retain a fetus diagnosed as male or female. Of 700 prenatal diagnoses undertaken at one hospital in Western India between 1976 and 1977, 100% of fetuses diagnosed male contrasted to 5% of fetuses diagnosed female were carried to term (Ramanamma and Bambawale, 1980). We can not know how typical the sample for this controversial study is, but it does clearly document a continuing and drastic preference for sons in some parts of the world. The incidence of preferential male infanticide is certainly low, and its practice has been reported for 1-4% of human cultures (Minturn and Stashak, 1982; Whyte, 1978).
Even where parents do not practice outright infanticide, other forms of sex-biased investment by parents are widespread. As Johansson (this volume, Chapter 4) points out, differential provisioning of sons and daughters is one of the primary modes of biasing parental investment. Reports of one sex or the other being nursed longer are common in the ethnographic and historical literature, and such phenomena are almost certainly underestimated. Among the Wolof of West Africa, for example, females are said to be breast-fed up to 24 months, while males are nursed 18 months (Falade, 1971; cf. Burrows and Spiro, 1957, for the Ifaluk case; Orent, 1975, for the Kafa of Southwest Nigeria; Miller, 1981:90, for various Moslem Middle Eastern examples). The most widely spread bias, however, particularly in Asia, parts of Latin America, and occasionally Europe, appears to be in favor of feeding males more. For a sample of 422 Lebanese infants from the Middle East in a culture where sons are regarded with greater âwarmthâ than daughters, Prothro reports: âIn every group [studied] there were more girls than boys breastfed for less than five months and more boys than girls for more than fourteen monthsâ; these trends were statistically significant (Prothro, 1961:74; see also Tekçe and Shorter, 1984, for Jordan). The nursing ideal for ninth-century France closely resembles that for contemporary Ecuador: Daughters should be nursed an average of 1 year, boys twice that long (McKee, 1982; Coleman, 1976; see also Margery Wolf for Taiwan, cited in McKee, 1982; Gessain, 1963, for Guinea; Khan, 1973, for Northern India). Similar biases are suggested by data on birth spacing where the span of time until the next infant is born is longer after a son than after a daughter (Haldar and Bhattacharyya, 1969; Khan, 1973).
The connection between early weaning and mortality is indirect and therefore difficult to prove. In my opinion, however, there can be little doubt that early curtailment of breast-feeding and the double loss of both nutritional and immunological benefits of motherâs milk renders infants more susceptible to rotavirus and other sources of diarrhea, the worldâs major mortality threat to infants in undeveloped countries (Blacklow and Cukor, 1981). Preferential feeding of sons can be viewed as potentially lethal discrimination against daughters. At the same time the alternative possibility, that parents are merely trying to compensate for the greater vulnerability of males by feeding them better or feeding them longer, must also be kept in mind, a point that will be returned to.
Traditional explanations for parental sex preferences, particularly the widespread preference for sons in many cultures (Coombs, 1977; Miller, 1981; Park, 1983) stress: (1) the greater strength of males and their essential contributions to hunting and heavy agricultural work; (2) their importance as warriors and in local disputes; (3) male roles in rituals and in transmission of family names; (4) high cost of dowries in those societies that have dowries (at a bare minimum, 8% of human cultures); and (5) high value placed on males for âideologicalâ reasons.
There can be little doubt that such factors do indeed play a role. Strong arguments can be marshalled to explain preferential female infanticide among groups like the Copper Eskimo in terms of the importance of hunting by males or female infanticide among the Yano-mamo in terms of the importance of sons needed to wage war and to successfully raid for wives (Balikci, 1967; Chagnon, 1968; see also Divale and Harris, 1976). The ideological arguments, and especially arguments based on male roles in rituals, and dowries, are more problematic simply because one suspects that a strong preference for sons preceded the establishment of these institutions. Similarly the hypothesis that female infanticide can be attributed to low female participation in subsistence (e.g., Miller, 1981) leaves much to be explained, particularly its occurrence in areas where females work very hard and its absence in some areas where women work little.
The failure of traditional explanations to explain a large portion of the known cases of sex bias have led some authors (e.g., Härtung, 1983; Dickemann, 1979a) to consider a sixth explanation, essentially a sociobiological explanation that focuses on the probable reproductive contribution of sons versus daughters under different socioecological conditions. In this realm, the most logically powerful tool to date has been what is now known in evolutionary biology as the âTrivers-Willard hypothesis.â
It should be noted that the Trivers-Willard hypothesis is a very broad one insofar as it applies across species, to many animals as well as to humans; it is also narrow in that it applies only under specialized conditions (detailed in the next section). Even if valid, the Trivers-Willard hypothesis is not going to provide an explanation for all sex-biased investment by parents. Nevertheless, I would contend that to explain even a portion of cases in which parents terminate investment in one sort of offspring while investing in another represents a significant advance in an area where general theories have not previously been used. For the most part, the Trivers-Willard hypothesis has been ignored out of hand by most or else cited as a proved âtheoryâ by a very few. This chapter provides a critical and comprehensive examination and evaluation of the success this hypothesis has had in explaining sex-biased parental investment by parents in primates (including humans) and other mammals.