Olav Oftedal

Black bears give birth and lactate during the 2–3-mon fast of winter dormancy. Thereafter the female emerges from the den with her cubs and begins to feed. We investigated fatty acid patterns of milk from native Pennsylvania black bears during the period of winter dormancy, as well as after den emergence. Throughout winter dormancy, milk fatty acid composition remained relatively constant. The principal fatty acids at all times were 14∶0, 16∶0, 16∶1, 18∶0, 18∶1, 18∶2n−6, 18∶3n−3 and 20∶4n−6. After den emergence, large changes occurred in almost all the fatty acids, particularly in 18∶2n−6 and 18∶3n−3. Large variability among the active free-ranging animals likely reflected differences in diet. In a carnivore, with apparently limitedde novo synthesis of fatty acids, milk fatty acid composition may be affected by factors such as transition from reliance on stored lipids to feeding, and by temporal changes in dietary intake.

Observed changes in maternal investment due to an environmentally induced decrease in food supply (the 1983 El Niño-Southern Oscillation) are compared witha priori predictions for the California sea lion (Zalophus californianus). Changes in behavior, growth and mortality of off-spring were also examined. Data collected in the first two months postpartum for the years before (PRE), during (EN), and the two years after (POST1 and POST2) the 1983 El Niño indicate that females initiated postpartum feeding trips earlier during the food shortage, and spent more time away on individual feeding trips in both the El Niño year and the year after. Perinatal sex ratios (♀:♂) in the years PRE, EN, POST1 and POST2 were 1:1, 1.4:1, 1.1:1 and 1:1.4, respectively. Fewer copulations were observed during the El Niño year, but this difference was not statistically significant. Pups spent less time suckling in the food shortage year and the year following, but attempted to sneak suckle more. Pups were less active and played on land less in the El Niño and following year. Finally, maternal investment as measured by milk intake of offspring was decreased, pups grew more slowly, and suffered increased mortality during the food shortage year. Despite expected sex differences in maternal investment and pup behavior in response to food shortage, there were no sex-biased differences in response in either females or pups. As expected, the food shortage did not affect adult males since they migrate north during the non-breeding season where the environmental perturbation was less severe.

ABSTRACT We hypothesized the vitamin D-deficient green iguanas with depleted calcium stores would seek to augment calcium intake by self-selection of a high calcium source. Eight green iguanas were offered free-choice ground oystershell in addition to their regular diet. Of these, two had not been exposed to ultraviolet (UV-B) radiation for > 5 years and were demonstrated to be vitamin D-deficient by low circulating levels of the principal vitamin D metabolite, calcidiol (25-hydroxy-cholecalciferol). The six others had been exposed to a UV-B emitting bulb for the previous 3 years and had high circulating calcidiol levels. Average daily food intake (expressed as dry matter per kg body mass) did not differ between the Low-D and High-D iguanas. The daily oystershell intake of the Low-D iguanas (0.02–0.03 g/kg) was lower than that of the High-D iguanas (0.06–0.70 g/kg), leading to a significant difference in calcium intake. The failure of iguanas to increase calcium intake in response to vitamin D-deficiency was puzzling and suggests that vitamin D, as a steroid hormone, may play some role in the expression of calcium appetite. Zoo Biol 16:201–207, 1997. © 1997 Wiley-Liss, Inc.

Lactation appears to be an ancient reproductive trait that predates the origin of mammals. The synapsid branch of the amniote tree that separated from other taxa in the Pennsylvanian (>310 million years ago) evolved a glandular rather than scaled integument. Repeated radiations of synapsids produced a gradual accrual of mammalian features. The mammary gland apparently derives from an ancestral apocrine-like gland that was associated with hair follicles. This association is retained by monotreme mammary glands and is evident as vestigial mammary hair during early ontogenetic development of marsupials. The dense cluster of mammo-pilo-sebaceous units that open onto a nipple-less mammary patch in monotremes may reflect a structure that evolved to provide moisture and other constituents to permeable eggs. Mammary patch secretions were coopted to provide nutrients to hatchlings, but some constituents including lactose may have been secreted by ancestral apocrine-like glands in early synapsids. Advanced Triassic therapsids, such as cynodonts, almost certainly secreted complex, nutrient-rich milk, allowing a progressive decline in egg size and an increasingly altricial state of the young at hatching. This is indicated by the very small body size, presence of epipubic bones, and limited tooth replacement in advanced cynodonts and early mammaliaforms. Nipples that arose from the mammary patch rendered mammary hairs obsolete, while placental structures have allowed lactation to be truncated in living eutherians.

Although it has been more than one hundred years since the first publication on the milks of whales and dolphins (Order Cetacea), information on lactation in these species is scattered and fragmentary. Yet the immense size of some cetaceans, and the recent evidence that another group of marine mammals, the true seals, have remarkable rates of secretion of milk fat and energy, make this group of great comparative interest. In this paper information on lactation patterns, milk composition and lactation performance is reviewed. Two very different patterns are evident. Many of the baleen whales (Suborder Mysticeti) have relatively brief lactations (5–7 months) during which they fast or eat relatively little. At mid-lactation they produce milks relatively low in water (40–53%), high in fat (30–50%), and moderately high in protein (9–15%) and ash (1.2–2.1%). From mammary gland weights and postnatal growth rates, it is predicted that their energy outputs in milk are exceptional, reaching on the order of 4000 MJ/d in the blue whale. This is possible because pregnant females migrate to feeding grounds where they can ingest and deposit great amounts of energy, building up blubber stores prior to parturition. On the other hand, the toothed whales and dolphins (Suborder Odontoceti) have much more extensive lactations typically lasting 1–3 years, during which the mothers feed. At mid-lactation their milks appear to be higher in water (60–77%) and lower in fat (10–30%) and ash (0.6–1.1%), with similar levels of protein (8–11%). At least some odontocetes resemble primates in terms of low predicted rates of energy output and a long period of dependency of the young. However, these hypotheses are based on small numbers of samples for a relatively small number of species. Much of the available data on milk composition is of rather poor quality; for example, it is not possible to determine if milk composition changes over the course of lactation among odontocetes. Additional research on cetacean mammary glands and their secretions is needed to understand the reproductive strategies of these fascinating animals.

Although lactation is accompanied by increased nutrient demands for milk synthesis, many species of bears, true seals, and baleen whales fast for much or all of lactation. Large body mass in these species confers the advantage of greater stores of fat and protein relative to rates of milk production. Given the constraints on substrate availability during fasting, the milks of fasting mammals are predicted to be low in carbohydrate, protein, and water and to be high in fat. The milks of bears, true seals, and baleen whales conform to this prediction. Mammals that lactate while fasting may lose up to 40% of initial BW. The production of milk entails the export of up to one-third of body fat and 15% of body protein in the dormant black bear and in several seal species, which greatly depletes maternal resources and may represent a physiological threshold, because higher protein and fat outputs have only been measured in species that start feeding. The low K:Na ratio of seal and whale milks and the low Ca:casein and inverse Ca:P ratios in seal milks are unusual and warrant further study.

ABSTRACT Hypothesized relationships between milk composition and life history traits were examined by analyzing mid-lactation milks of seven lemurs (Eulemur fulvus, E. macaco, E. rubriventer, E. mongoz, Varecia variegata, Hapalemur griseus, Lemur catta), three bushbabies (Otolemur crassicaudatus, O. garnettii, Galago moholi), and two lorises (Nycticebus coucang, Loris tardigradus); partial data were also obtained for the lemuroid Cheirogaleus medius. There were significant differences in milk composition among species within either Eulemur or Otolemur, but the four genera for which multiple samples were available (Eulemur, Varecia, Otolemur, and Nycticebus) exhibited large composition differences. Eulemur milk was, on average, very dilute (9.9% dry matter) and low in energy (0.49 kcal/g). These milks contained 0.9% fat, 1.2% protein, and 8.4% carbohydrate on a fresh weight basis. Protein energy comprised only about 15% of total milk energy. Varecia had significantly higher dry matter (13.5%), fat (3.2%), protein (4.2%), gross energy (0.80 kcal/g), and protein energy: total energy ratio (28%) than Eulemur. Milks of the lorisoid genera Otolemur and Nycticebus were very similar, and both had significantly higher dry matter (18.3, 16.3%), fat (7.6, 7.0%), and gross energy concentration (1.27, 1.13 kcal/g) than either lemuroid genus. Otolemur milk was higher in protein than Nycticebus milk. We conclude that lorises, bushbabies, and perhaps cheirogaleids produce relatively rich, energy-dense milks in comparison with anthropoid primates. However, dilute milks appear to be uniformly found among species of Eulemur and perhaps in Lemur catta. The milk of Varecia (and perhaps Hapalemur) is intermediate in composition. Differences in milk composition among prosimians may be related to differences in maternal care: prosimians that carry their young during lactation produce more dilute milks than do species which leave their young unattended for prolonged periods. When looking at primates as a whole, however, the picture is somewhat less clear, since the milks of some “parkers” like Varecia do closely resemble those of large anthropoid primates who carry their young. Am. J. Primatol. 41:195–211, 1997. © 1997 Wiley-Liss, Inc.

A digestion trial with subsequent examination of feed selection was conducted using two captive giraffe fed four feedstuffs. Apparent digestibility coefficients were relatively high, indicating that the animals were efficiently utilizing the feedstuffs. However, values could be affected by the possible ingestion of soil containing acid-insoluble ash. A high fiber pelleted feed was eaten in a greater quantity than a low fiber feed, even though the constituents in each feed were the same. Gross energy content of residual hay was higher than gross energy content of the offered hay. whereas neutral detergent fiber and acid detergent fiber content were lower in the residual than in the offered hay. The animals did not appear to be selecting for a diet high in energy or low in fiber. Based on these results and other information, re-classification of giraffe as a facultative concentrate selector or as an intermediate feeder may be appropriate.

We examined the relationship between lactation performance and infant growth in a captive population of common marmosets (Callithrix jacchus) that varied in both maternal and litter size. Though common marmosets display a typical primate pattern of dilute milk and relatively slow infant growth rates (factors associated with low daily lactation investment and minimal maternal size effects), we hypothesized that the marmoset's small body size would make lactation investment more sensitive to maternal size than is true for larger-bodied primates. Smaller mothers rearing twins had lower milk fat, lower gross energy in milk samples collected in mid to late lactation and lower nursing-bout frequencies than did large mothers nursing twins. Lactation performance and maternal behavior did not differ between large and small mothers when rearing singletons, with a single exception: small mothers had a lower gross energy in mid-lactation milk samples. Relative growth rates in twins but not singletons were affected by maternal size, such that small mothers supported more growth per infant when rearing singletons while large mothers supported more growth per infant when rearing twins. Among the larger mothers, only, older mothers supported somewhat, though not significantly, less growth per infant, regardless of litter size. Twin infants of small mothers appeared to respond to below-optimal levels of milk yield by initiating maternal carrying less often. The relative energy intake of mothers was similar regardless of litter or maternal size. Small mothers rearing twins drew more heavily on reserves, reflected in a linear weight loss during lactation; however, the reserves drawn upon were inadequate to meet the lactation demand, resulting in lower milk energy output. In addition, small mothers rearing twins were more likely to be ill and less likely to be fertile in the year following lactation than were large mothers of twins or mothers of any size rearing singletons.

Significant relations were observed between select infant-care and weaning behaviors and growth in body weight in common marmoset monkeys (Callithrix jacchus). The patterns of these relations suggest that earlier occurrence of developmental milestones, such as cessation of transport (being off carriers) and weaning to solid food, were associated with slower growth during the subsequent period. In contrast, more frequent nursing bouts during the period in which weaning was initiated were associated with higher growth rates. In the case of being off carriers, these effects did not carry over to older ages, suggesting that any deficits in growth were temporary. In the case of earlier, more frequent consumption of solid food, there was some suggestion that there were longer-term effects, followed by catch-up growth. The knee-to-heel length of subjects was not related to the measured behaviors. There was no relation between early weaning to solid food and leanness at day 75, suggesting that, although this behavior was affecting overall weight, it did not affect relative gains of fat versus lean mass. There were, however, significant correlations between cessation of transport or frequency of nursing bouts during the weaning period and leanness, with earlier cessation of transport and less frequent nursing associated with leaner infants, after weaning. Our results differed from those of a previous study that found a relation between linear growth and abuse in this species, with abuse defined as physical injury by other members of the group. We found no differences in growth between abused and nonabused infants. However, abused infants had lower birth weight.