The reproductive biology of female Père David's deer (Elaphurus davidianus)

Data for this study came from breeding records of 27 Père David's (Elaphurus davidianus) hinds maintained in large pastures and from estrous records of four hand-reared nulliparous hinds. The mean estrous cycle length ranged from 17.5 to 19.6 days. Standing estrus resembled that of other cervids, except that a low, moaning vocalization was given in response to contact, and activity (as measured by pedometers) did not increase. Mean gestation length was 183.38 ± SD 6.11 days (n = 21), and nearly all females conceived in the second and third years. The median interbirth interval was 362 days. The median birth date was April 8, and 80% of the births occurred over a 9.5-week period. Multiparous hinds gave birth an average of 20.5 days earlier in the season than primiparous hinds. There was no dimorphism in birth weight. The results are discussed in light of comparative data for other species.     

Reproduction of the mongoose lemur (Lemur mongoz) in captivity

Responses to questionnaires sent to 20 institutions holding Lemur mongoz did not reveal which aspects of management or husbandry could account for reproductive failure in the captive population, but allowed some qualitative comparisons with data compiled for captive and wild animals. In general, reproduction has occurred initially among wild-caught specimens before tapering off, and rarely occurs in the captive F₁ generation. Data compiled by the International Species Inventory System and the International Zoo Yearbook revealed an aging captive population with no recent reproduction. No aspect of group composition, activity patterns, seasonal light regime, reproductive cycles, or diet could be linked to the lack of reproduction; and among lemurs subjected to the same conditions, some were known to reproduce while others did not. Lack of knowledge about this species and the threat of extinction for both captive and wild populations make an investigation of reproductive biology imperative. Recommendations for a research program are given.     

Optimal group size and seasonal stress in ring-tailed lemurs (Lemur catta)

Adaptive explanations for social grouping assume that thereare fitness consequences associated with group size, and individualsmaintain membership in groups of favorable size to maximizefitness. Here I examine fecal cortisol concentrations as a hormonalmeasure of stress to assess the relative well-being of Lemurcatta in groups of different size and in seasons of normal andlow tamarind fruit availability. I test the hypotheses thatthere is an optimal group size at which cortisol is lowest andthat optimal group size changes in food-scarce conditions. Icollected 799 fecal samples from 87 individuals in seven free-rangingL. catta groups at Berenty Reserve, Madagascar, over a 1-yearperiod (August 1999–July 2000) and determined fecal cortisolconcentrations using a radioimmunoassay. Expressing these asresiduals from monthly population means to control for temporalfluctuations in cortisol concentration, I calculated mean fecalcortisol levels for each animal in seasons of normal and lowtamarind fruit abundance and over the entire year. Overall,females exhibited lowest mean cortisol levels in groups of intermediatesize, suggesting that there are benefits to maintaining membershipin these groups. Females in groups that were atypically largeor small for their habitat type had higher mean cortisol levelsthan typical groups. Cortisol levels increased in food-scarceconditions for larger groups, suggesting that intergroup competitiveadvantages do not outweigh intragroup feeding competition atthis time. Group size may be optimized for long-term averageconditions, and short-term stresses may intermittently alterthe costs associated with group size.     

Correlates between locomotor anatomy and behavior in two sympatric of Lemur.

Sympatric populations of Lemur catta and Lemur fulvus show major differences in their occupation of canopy forest levels. Lemur catta is usually found in the lowest levels of the forest, and uses the ground for travel over 65% of the time. Lemur fulvus uses the upper levels of the canopy forest and is observed on the ground in less than 2% of all observations. Comparison of hindlimb musculoskeletal anatomy show statistically significant differences in the lengths of the long bones and the height of the talus. Differences also occur in ranges of tibio-talar and mid-talar joint mobility. The details of insertion of the biceps femoris muscle are distinct in the two species as is the relative mass of muscle associated with flexion of the pedal digits, and flexion of th tibio-talar joint. The metric and morphological differences in the hindlimb anatomy of Lemur catta and Lemur fulvus are consistent with differences in habitat and substrate utilization.     

Experimental litter size reduction reveals costs of gestation and delayed effects on offspring in a viviparous lizard

Experimental studies have often been employed to study costs of reproduction, but rarely to study costs of gestation. Disentangling the relative importance of each stage of the reproductive cycle should help to assess the costs and benefits of different reproductive strategies. To that end, we experimentally reduced litter size during gestation in a viviparous lizard. We measured physiological and behavioural parameters during gestation and shortly after parturition, as well as survival and growth of females and their offspring. This study showed four major results. First, the experimental litter size reduction did not significantly affect the cellular immune response, the metabolism and the survival of adult females. Second, females with reduced litter size decreased their basking time. Third, these females also had an increased postpartum body condition. As postpartum body condition is positively related to future reproduction, this result indicates a gestation cost. Fourth, even though offspring from experimentally reduced litters had similar weight and size at birth as other offspring, their growth rate after birth was significantly increased. This shows the existence of a maternal effect during gestation with delayed consequences. This experimental study demonstrates that there are some costs to gestation, but it also suggests that some classical trade-offs associated with reproduction may not be explained by gestation costs.     

Reproductive biology and management of captive black-footed ferrets (Mustela nigripes)

A captive breeding program is being conducted with black-footed ferrets (Mustela nigripes), an endangered species. Results of 5 years of study are reported. Simple, but specialized, nontraumatic handling techniques allowed assessment of reproductive status with minimal stress, which was important in breeding management. Black-footed ferrets are sexually mature and may successfully reproduce in their 1st year. Proestrus lasts approximately 2-3 weeks. Duration of estrus in unbred females was 32–42 days; females usually bred within 20 days. Most breeding activity occurred during April. Mean gestation length was 42.7 days (±0.7, range 42–45 days), litter size averaged 3.0 kits (±1.4, range 1–6 kits), and weaned kits/litter averaged 2.4 (±1.7, range 1–6 kits). Weaning rate of kits was 80%. Sex ratio of kits was essentially 1:1. Productivity was greatest among females ?3 years of age. Rapid expansion of the captive population is possible and will be important for genetic management of the species and for achieving the primary goal of the recovery program, which is to return black-footed ferrets to the wild.     

Selected aspects of female white-faced saki (Pithecia pithecia) reproductive biology in captivity

Little is known regarding the reproductive biology of the white-faced saki. Although sakis have been in zoos since the mid-1970s, little attention has been paid to the reproductive biology of this threatened species. This study describes the results of a 3-year study of the reproduction of the white-faced saki in captivity. Using noninvasive methods to determine levels of estrone conjugates (E₁C) and pregnanediol-3-glucuronide (PdG) in daily urine samples, we have characterized the female reproductive cycle of this species. Nonconceptive ovarian cycles were 16.95 ± 1.57 (SD) days, gestational length was 146.1 ± 5.2 (SD) days, and the length of lactationally induced infertility varied among females but averaged 163 ± 40.6 (SD) days. Attempts to accelerate puberty by pairing a young female with an adult male was without effect. Puberty occurred at 32 months of age in one female. This study provides information that enhances our understanding of the reproductive biology of this species. © 1995 Wiley-Liss, Inc.     

Contrasting reproductive parameters ingalago senegalensis braccatus andG. s. moholi

Reproductive parameters were compared between two subspecies of the lesser bushbaby, Galago senegalensis braccatusand G. s. moholi.Adult body weights for both male and female G. s. braccatuswere significantly higher than adult body weights of G. s. moholi,as were infant birth weights. The mean gestation length of G. s. braccatuswas significantly longer than that of G. s. moholi. G. s. moholihad a higher incidence of twinning than G. s. braccatus.Puberty in females occurred significantly later in G. s. braccatusthan in G. s. moholi.These differences are of such magnitude that hybridization of G. s. braccatuswith G. s. moholiwould be unlikely. These differences, if augmented by additional evidence, may warrant distinction of the two subspecies at the species level.     

Research on reproductive biology of gorillas

Laboratory research has implicated several variables which contribute to the regulation of reproductive behaviour of captive gorillas. Females were found to be increasingly attractive to males during the follicular phase of the menstrual cycle when estrogen and testosterone concentrations in the female were increasing. Females solicited mating from the males primarily at midcycle, about the time when the concentration of testosterone was maximal. No mating occurred during the mid- to late luteal phase after progesterone concentrations were elevated. Both males and females initiated mating during the midcycle, periovulatory period, but male initiative accounted for most mating that was temporally dissociated from that period. Individual differences between males and among females contributed to the variability in results. Confinement of a male and female in relatively small quarters appears to interact with certain aspects of species-typical behaviour to distort patterns of mating in laboratory tests. Data on behaviour of gorillas in the wild contributed to interpretation of the laboratory results and suggest an enlightened approach to the captive maintenance and breeding of gorillas. An important consideration in promoting captive breeding of gorillas seems to be the provision of options to the female for regulating the frequency and distribution of mating in the cycle.     

Unit pricing: Economics and the evolution of litter size

Variability in litter size and the concept of optimality are central to our current understanding of parental investment patterns and life histories. A fundamental component of most models of optimum litter size is an apparently inescapable trade-off between litter size and size of offspring. Most previous models of litter size have focused on the evolution of an optimum litter size rather than variability in litter size. Because variability provides the raw material from which numerous optimal litter sizes are fashioned to meet prevailing conditions, approaches that specifically address adaptive patterns of variability might provide new insights into the evolution of litter size. A model based on a non-linear relationship between total parental effort and litter size reduces trade-offs between offspring size and offspring number to simple reproductive economics, and illustrates how litter size variability might be predictable under certain environmental conditions. This revised version was published online in July 2006 with corrections to the Cover Date.     

Reproduction in the slow loris (Nycticebus coucang)

The reproductive biology of the slow loris (Nycticebus coucang) is poorly documented because of infrequent captive breeding success and the absence of field studies of this species. Reproductive data were collected from a breeding colony of slow lorises held at the Duke University Primate Center for the past 10 years. Nineteen infants were born, with a sex ratio of 1:1 and a neonatal mortality rate of 15.8%. In all cases, litter size was one. Females born in the colony copulated for the first time between 18 and 24 months of age. A male that reached sexual maturity in the colony sired his first offspring at the age of 17 months. Estrous cycles ranged in duration from 29–45 days, with copulations usually occurring for 1 day of estrus. Gestation length averaged 192.2 days. Although a postpartum estrus was observed in three cases of infant death, no conceptions resulted. Lactation lasted approximately 6 months. A clear birth peak was observed, with 12 out of 19 births occurring in March, April, and May. The comparatively low basal metabolic rate of this species may account for the unusually low reproductive rate of the slow loris in comparison with other prosimian primates.     

Life History Variation in Female Gambusia hubbsi

Gambusia hubbsi populations occur in a variety of fresh and brackish-water habitats on Andros, Bahamas. These include shallow water sites (tidal creeks, lakes, roadside ditches), and blueholes (vertical solution caves). In some blueholes G. hubbsi is the only species present, in others it co-occurs with other species, principal among these is a predator, Eleotris pisonis. By contrast to blueholes, shallow water sites have highly variable temperature and depth. In addition, they are frequented by avian piscivores and may be occasionally occupied by piscivores such as Eleotris. We sampled 10 shallow water sites, 14 blueholes where Eleotris is absent and 12 blueholes where Eleotris co-occurs with G. hubbsi. We measured and compared variation in female body size, fecundity, and reproductive investment among these three habitats. The observed patterns of life history variation are only partially in accord with expectations from theory regarding the effects of predation and seasonality on life history variation. Samples from populations that colonized a series of man-made trenches (Well Fields), a set of introductions into that habitat, and changes in life history traits of lab-raised females from three blueholes, suggest that the observed pattern of life history variation in other habitats also reflects differences in food availability among habitats, and imperfectly reflects the potential phenotypic variability of this species.     

The role of scent marking in Lemur catta agonistic behavior

Certain forms of marking behavior in Lemur catta have been considered to be aggressive in nature but had not been analyzed specifically in this respect. This study examines the relationship between the occurrence of all forms of marking behavior displayed by a captive group of lemurs and their physical and nonphysical aggressive interactions. All forms of marking behavior, especially males' tail mark and tail wave displays, were found to correlate with aggressive behavior including female-instigated agonism. In comparison, allogrooming, a behavior thought not to have an agonistic component, was not significantly correlated with any marking nor agonistic category. The data suggest that in intersexual interactions male marking behavior is an aggressive but nonphysical substitute for physical aggression toward females who have generally been regarded as dominant to males in this species.     

The influence of ambient salinity on routine metabolism in the teleost Cyprinodon variegatus Lacepède

Routine metabolism of the euryhaline cyprinodontid Cyprinodon variegatus Lacepede was measured at a series of ambient salinities ranging from fresh water through 100‰. Fish used had been sequentially acclimated to the test salinities (ambient temperature of 20±1° C and a 12: 12 L: D schedule).
Routine metabolic rates were highest at ambient salinities from 15 to 50‰. Metabolism was somewhat lower at ambient salinities less than 15‰, and showed a sequential decline at ambient salinities greater than 50‰. It is suggested that routine metabolism is depressed at elevated salinities by reduced O, transfer, a consequence of maintenance of hydromineral balance in hypersaline waters.