Reproductive parameters of a captive colony of capuchin monkeys (<Emphasis Type="Italic">Cebus apella</Emphasis>) from 1984 to 2006

This paper presents the results of a demographic analysis of 22 years of data recorded on a colony of tufted capuchin monkeys (Cebus apella) in captivity at the CNR Primate Centre (Rome, Italy). Information is provided on reproduction, sex ratio, inter-birth interval (IBI), seasonality, and body weight. From 1984 to 2006, 46 live births were recorded. There were births in almost all months of the year, but a higher frequency was observed during spring and summer (71.1%). The sex ratio was 1:1 M:F for newborns and 1:1.06 M:F for surviving offspring. At birth, infants’ average weight was 238.13 ± 37.51 g, i.e. 250 ± 56.79 g for males and 231 ± 26.08 g for females. Age at first birth for females ranged from 4.9 to 7 years (n = 9), while males achieved first paternity between the ages of 5 and 9.2 years (n = 6). Only one pair of twins was recorded during this period. For females, the mean IBI was 17.88 ± 1.84 months, when they reared infants, and 12.70 ± 1.73 months, when they did not rear offspring. Infant mortality within the first 2 months was 28.3%.     

Pubertal weight gain in female rhesus macaques

In order to describe the timing and extent of accelerated pubertal weight gain in female rhesus, we examined a large colony data base consisting of over 10,000 weight records for animals between 1.5 and 3.0 years of age (menarche occurs at about 2.6 years). Average colony weights were determined by week of age from information on age at weighing. Cross-sectional analyses with linear regression demonstrated an acceleration in weight increase from 196 to 231 weeks (28–33 months) when colony weights increased 381 g/12 weeks as opposed to an average of 193 and 203 g, respectively, during the preceding and succeeding age intervals of the same length. Longitudinal analyses (n = 428) indicated that maximum individual growth velocity averaged 499 ± 18 g/12 weeks and occurred at 119 ± 5.6 weeks (29.7 ± 0.2 months) of age. Nonlinear modeling with the Gompertz function indicated that decelerating growth rates seen at earlier ages were not characteristic of the period of accelerated pubertal growth. © 1996 Wiley-Liss, Inc.     

Age at Puberty and the Emerging Obesity Epidemic

Background

Recent studies have shown that puberty starts at younger ages than previously. It has been hypothesized that the increasing prevalence of childhood obesity is contributing to this trend. The purpose of this study was to analyze the association between prepubertal body mass index (BMI) and pubertal timing, as assessed by age at onset of pubertal growth spurt (OGS) and at peak height velocity (PHV), and the secular trend of pubertal timing given the prepubertal BMI.

Methodology/Principal Findings

Annual measurements of height and weight were available in all children born from 1930 to 1969 who attended primary school in the Copenhagen municipality; 156,835 children fulfilled the criteria for determining age at OGS and PHV. The effect of prepubertal BMI at age seven on these markers of pubertal development within and between birth cohorts was analyzed. BMI at seven years was significantly inversely associated with age at OGS and PHV. Dividing the children into five levels of prepubertal BMI, we found a similar secular trend toward earlier maturation in all BMI groups.

Conclusion/Significance

The heavier both boys and girls were at age seven, the earlier they entered puberty. Irrespective of level of BMI at age seven, there was a downward trend in the age at attaining puberty in both boys and girls, which suggests that the obesity epidemic is not solely responsible for the trend.     

Genome‐scan analysis for genetic mapping of quantitative trait loci underlying birth weight and onset of puberty in doe kids (Capra hircus)

The objective of this study was to locate quantitative trait loci (QTL) causing variation in birth weight and age of puberty of doe kids in a population of Rayini cashmere goats. Four hundred and thirty kids from five half‐sib families were genotyped for 116 microsatellite markers located on the caprine autosomes. The traits recorded were birth weight of the male and female kids, body weight at puberty, average daily gain from birth to age of puberty and age at puberty of the doe kids. QTL analysis was conducted using the least squares interval mapping approach. Linkage analysis indicated significant QTL for birth weight on Capra hircus chromosomes (CHI) 4, 5, 6, 18 and 21. Five QTL located on CHI 5, 14 and 29 were associated with age at puberty. Across‐family analysis revealed evidence for overlapping QTL affecting birth weight (78 cM), body weight at puberty (72 cM), average daily gain from birth to age of puberty (72 cM) and age at puberty (76 cM) on CHI 5 and overlapping QTL controlling body weight at puberty and age at puberty on CHI 14 at 18–19 cM. The proportion of the phenotypic variance explained by the detected QTL ranged between 7.9% and 14.4%. Confirming some of the previously reported results for birth weight and growth QTL in goats, this study identified more QTL for these traits and is the first report of QTL for onset of puberty in doe kids.     

Body weight as an effective tool for determination of onset of puberty in captive female Nile hippopotami (Hippopotamus amphibious)

Profiles of fecal progestogens and body weight from the early juvenile to the peri‐pubertal period are presented for eight captive female Nile hippopotami housed at Disney's Animal Kingdom in Florida. Average growth rate in juveniles was 0.85±0.03 kg/day (r²=0.913). Progestogen elevations were detectable as early as 16.8 months of age, and elevations indicative of ovulation and luteal activity were identified in seven of eight females by 30.3±1.6 months of age and body weight of 829.3±49.4 kg. Progestogen patterns before the onset of puberty were highly variable within and between females. Some females remained at baseline concentrations, whereas in others the progestogen pattern was characterized by infrequent, transient elevations of low amplitude and shortened duration. Four females were monitored through onset of puberty, conception, and first pregnancy. Onset of puberty was defined as the first luteal phase from the series of consecutive ovarian cycles culminating in conception and was observed at 34.9±2.2 months of age and 963.6±39.4 kg, however, the quality and number of cycles varied among females before conception. Females conceived between 2.7–3.9 years of age after attaining an approximate threshold body weight of 1,000 kg (1,070.5±39.5 kg). The age at first conception in captivity occurs at a younger age than has been reported for wild populations. Body weight may be an effective tool for approximating the state of reproductive maturity and facilitate collection management in zoos. Zoo Biol. 0:1–13, 2005. © 2005 Wiley‐Liss, Inc.     

Population ecology of rhesus monkeys (Macaca mulatta) at Nanwan Nature Reserve,Hainan, China

Rhesus monkeys (Macaca mulatta) at the Nanwan peninsula of Hainan Island, China, have been observed in the field for 25 years, and have been studied intensively for eight years, beginning in 1981. There were about 115 monkeys in 5 natural groups when the Nanwan Reserve was founded in 1965. From 1965 to 1984, the number of groups increased from 5 to 19, and the total population increased from 115 to 930 individuals, an annual population increase of 12.7%. From 1984 to 1987, the population continued a slower rate of increase (8.9%) to approximately 1200 monkeys in 20 groups. The home ranges of each monkey group at Nanwan varied from 0.16 to 0.72 km², with a mean and standard deviation of 0.37 ± 0.18. The size of the home range of the rhesus was affected by the quality of vegetation and rhesus population density. The average birth rate per year was 77.8 ± 13.9%, varying from 53.8% to 100% since 1978. From 1978, the birth rates of two food provisioned groups were higher in alternate years (x? = 91.7%) and lower in intervening years (x? = 68.8%; P = <0.01). A minority (26.5%) of females have given birth at 4 years of age, most at 5 years. The sex ratio of newborns in any one year varied from 0.3 to 3.5 males to females, with a mean and standard error of 1.09 ± 0.37 males to females.     

Growth retardation in premenarchial female rhesus monkeys during chronic administration of a GnRH agonist (leuprolide acetate)

Abstract: Leuprolide acetate in depot form (0.75 mg/kg body weight/month, im) was administered to four female rhesus monkeys from 18–30 months of age, a period that includes the premenarchial growth spurt. They were compared to eight age matched controls. As anticipated, sexual maturation was blocked in the Leuprolide group and menarche did not occur. Growth was also severely retarded; no weight gain occurred during the study in the Leuprolide group as compared to a 25% weight gain (P = .004) in the control group. The Leuprolide group also lost muscle mass. Food intake normalized for body weight was not affected. Linear growth averaged 35% less in the Leuprolide group. Serum IGF-1 concentrations increased from 486±84 to 965±47 ng/mL (P = .0025) in the Leuprolide group and from 838±139 to 3,006±545 ng/mL (P = .0016) in the control group. These data suggest that premenarchial pituitary/gonadal suppression results in a distinctive pattern of growth retardation in monkeys.     

Treatment with 17β-oestradiol does not influence age and weight at puberty in Bos indicus heifers

The working hypothesis was that treatment of heifers with 17β-oestradiol (E₂) during specific periods of prepuberty would reduce the response of the hypothalamic–pituitary axis to E₂ negative feedback and induce an earlier onset of puberty. The effects of chronic treatment with exogenous E₂ administered at specific maturational phases on the age and weight at puberty were studied in 96 prepubertal Brahman (3/4–7/8 Bos indicus) heifers (187.0±3.3 days of age, mean±SEM), weighing 149.9±2.5 kg. Heifers were randomly assigned to one of six groups (n=16 per group). Groups 2–6 received E₂ implants (Compudose 200®) for 90-day periods starting at 10, 13, 16, 19 and 22 months of age, while animals in group 1 remained untreated. Implants were placed subcutaneously at the base of the ear. Blood was collected for progesterone (P₄) determination by radioimmunoassay (RIA) and the animals were weighed at monthly intervals from 6 to 15 months then weekly from 15 to 28 months of age. Puberty was defined by concentrations of P₄>1 ng/ml in plasma and identification of a corpus luteum (CL) by transrectal ultrasonography (Aloka 210DX:7.5 MHZ probe). Treatment with exogenous E₂ at any of the ages/treatment intervals evaluated in this study did not reduce age or weight at puberty (P>0.7). The mean age and weight at puberty of control heifers was 735.3±19.7 days (range: 597–861) and 299.2±10.2 kg (range: 233–382), respectively, which is greater than the age and weight at puberty of 481 days and 246 kg, that was previously reported for B. indicus heifers [Post, T.B., Reich, M.M., 1980. Puberty in tropical breeds of heifers as monitored by plasma progesterone. Proceedings of the Australian Society of Animal Production 13, 61–62.]. The large variation in age and weight at puberty that was observed in the present study among heifers might indicate an individual animal effect to E₂ treatment among some of the treated animals. The lengthy interval from birth to puberty observed in this study, as compared to other studies, reflects the effects of other factors such as genotype, environmental or nutritional influences on puberty.     

Growth curves of children with Down syndrome.

Growth curves of 105 children with Down syndrome (50 boys and 55 girls) were established. At birth height, weight and head circumference of Down syndrome children were lower than these parameters in controls. This delay remained stable until puberty. For weight there was no clear-cut pubertal growth spurt. For stature, the prepubertal growth spurt occurred earlier (at the age of 11 years in boys and 9 1/2 years in girls) than in controls but was less marked. As a result, Down syndrome patients had a short stature with a quite normal weight. These reference curves, available since prenatal diagnosis of Down syndrome is performed routinely, are helpful for monitoring normal and abnormal development in Down syndrome patients.     

Influences of month of birth and age on patterns of luteinizing hormone secretion in prepubertal heifers

An experiment was done to determine if month of birth and age influenced patterns of luteinizing hormone (LH) secretion in prepubertal heifers. Mean concentrations of LH increased linearly (P < .05) in March-born heifers between one and seven months of age. This was partially due to an increase in number of LH pulses. The prepubertal pattern of LH concentrations was quadratic (P < .05) for heifers born in September because concentrations were slightly higher (P = .15) than those in March-born heifers at one month of age. There were no differences between groups during the remainder of the prepubertal period (3 to 7 months). There was a tendency (P = .18) for September-born animals to reach puberty at younger ages than those born in March. September-born heifers also had greater (P = .06) average daily gains, but body weights at puberty were similar for the two groups. These results show that season of birth influenced LH concentrations at one month of age, but did not significantly affect the increase between three and seven months of age.     

Growth curves of body weight and their relationship to sexual maturity in laboratory-bred male African green monkeys (Cercopithecus aethiops)

Nonlinear growth models having a three- or four-parameter family were applied to individual body weight data of 5 male African green monkeys for estimating their growth patterns. Body weight was measured from birth to six years of age and 58 to 114 data items per monkey were collected. The average body weight at birth was 360g with the standard deviation of +/- 25g, 4.54 +/- 0.29 kg at five years of age, and 4.50 +/- 0.12 kg at six years of age at which point body weight was judged to have reached a plateau. Five growth models (Gompertz, Logistic, Richards, Bertalanffy and Brody) were applied to the growth data in this study. As a result, two (Gompertz and Logistic) of the five models were found applicable to all data from the five monkeys. However, the coefficient of determination (R2) obtained by application of the two models were not so large (0.919 +/- 0.05 in Gompertz, 0.889 +/- 0.01 in Logistic). Therefore the data were divided into two groups according to monkey age: the first group being from monkeys between birth and 2 years 10 months of age and the second group was from monkeys older than 2 years 10 months of age. The Gompertz model fitted best the data of the first group in four of the five animals (R2 = 0.982 +/- 0.011). The age at the inflexion point in the Gompertz model nearly corresponded to the age of weaning. The Logistic model was most suitable for the date of the second group in all five animals (R2 = 0.955 +/- 0.038).(ABSTRACT TRUNCATED AT 250 WORDS)     

Lack of pubertal influences on female dispersal in muriqui monkeys, Brachyteles arachnoides

The hormonal mediation of dispersal in female mammals is poorly understood, in part because of the difficulties of detecting the onset of ovarian cycling and puberty in dispersing individuals. We used noninvasive methods of faecal steroid assays to determine the timing of dispersal relative to puberty and ovarian cycling in wild female muriqui monkeys, a species in which males are philopatric and nearly all females transfer from their natal groups. Natal females had a mean+/-SE age of 73.4+/-7.2 months (N=18) at the time of their transfers. Intergroup transfers occurred when one or more sexually active adult females were present, but did not show any seasonal patterns. Faecal progesterone and oestradiol profiles from nine natal females prior to transfer and four non-natal females that transferred into our study group demonstrate unequivocally that dispersal occurs prior to puberty in this species. All females showed baseline oestradiol levels and low progesterone levels compared with cycling adult females. Immigrants were first observed to copulate at 11.2+/-2.2 months of age (N=4), prior to the onset of normal ovarian cycles, and gave birth to their first offspring at 33.8+/-7.3 months (N=4) after transferring. Mean cortisol levels did not differ between natal emigrants or recent immigrants, and were within the range of those of adult males during the nonbreeding season in 10 of the 11 prepubertal females sampled. These results indicate that female dispersal is not triggered by activational hormones associated with puberty or escape from reproductive suppression in this species. Copyright 2000 The Association for the Study of Animal Behaviour.     

Progressive deceleration in growth as an early sign of delayed puberty in boys

OBJECTIVE: To describe the prepubertal growth pattern in boys with delayed puberty. METHODS: Growth curves for height and height velocity covering the age range 4-14 years were constructed on the basis of retrospectively obtained data in 85 boys with delayed puberty, who attained a normal final height. RESULTS: Between the age of 4 and 14 years the height in this cohort progressively deviated from the normal reference. At the age of 4 years, the height SDS was already significantly lower (median -0.8; p < 0.001) and progressively diminished during childhood, resulting in a median height SDS of -1.1 at the age of 12 years (p < 0.001). The median final height of this cohort (-0.4) was not different from their target height (-0.2). The degree of deceleration in growth during childhood was not determined by birth weight or birth height and did not influence final height. The decline of the height velocity with age in this group of boys with delayed puberty was significantly smaller (p < 0.001) than predicted by the model of Rikken and Wit. CONCLUSION: Late-maturing boys often show a prepubertal deceleration in growth that starts at an early age but that does not affect final height.     

Effects of dry season nutritional supplementation on growth, onset of puberty and subsequent fertility in Boran and Boran x Friesian heifers in Ethiopia

Shortly after weaning at 8 months of age, 43 Boran and 46 Boran x Friesian crossbred heifers were randomly divided to either receive a supplementary feed containing 16% crude protein during the dry season or to serve as controls. Heifers were examined monthly, and data on body weight, wither height and body condition score were recorded. Ovarian size and structures were determined per rectum and heifers were kept under continuous observation for standing estrus. Blood samples were collected at 10-day intervals every month for determination of plasma progesterone levels. All heifers were exposed to intact bulls for 4 months after they attained 18 months of age. Average daily weight gain to puberty was significantly (P<0.01) higher in heifers given supplementation than in the controls (360 vs 326 g/day). The average daily weight gain in Boran heifers (296 g/day) was significantly (P<0.01) lower than in crossbred (392 g/day) heifers. Mean age at puberty differed significantly (P<0.001) between heifers given supplementation (573 days) and the controls (627 days). Boran heifers attained puberty at a significantly later age (660 vs 540 days; P<0.001) than crossbred heifers. Body weight at puberty did not differ between supplemented and control heifers (226 vs 222 kg); while the difference between Boran and crossbred heifers was significant (216 vs 232 kg; P<0.01). Pelvic size and body condition score were not influenced by supplementation but differed significantly between genotypes. Pregnancy rate after 4 months of breeding was higher in supplemented (79%) than in control (64%) heifers. Boran heifers had a significantly (P<0.001) lower pregnancy rate than crossbred heifers (52 vs 91%). Mean age and body weight at conception were not affected by supplementation but differed significantly (P<0.05) between genotypes. The results indicate that prepubertal supplementary feeding during the dry season increased growth rate, reduced age at puberty and improved fertility in both Boran and Boran x Friesian heifers.     

Age-related changes in body weight,scrotal size and plasma testosterone levels in buffalo bulls (Bubalus bubalis)

Body weight, testicle size and peripheral testosterone concentrations were measured in 35 water buffalo bulls at 5, 15, 17, 21, 25 and 38 months of age. These parameters were studied in all animals during the same month (October), so the changes due to age were independent of changes in photoperiod and temperature. Body weight increased linearly with age. The testicular size measured in terms of scrotal circumference as related to age, showed a curvilinear increase; the average rate of testicular growth was maximum between 15 and 25 months. Plasma testosterone levels were low between 5 and 21 months. A significant rise in plasma concentration of testosterone was observed at 25 months reaching peak levels at 38 months. The mean age of sexually mature bulls at the time of first ejaculation of semen with motile sperm, was 24.9±0.9 months (n=9). It has been concluded that in the Nili-Ravi buffalo bulls the sexually quiescent period (prepubertal) extends up to 15 months of age and sexual maturation as indicated by the presence of motile sperm in the ejaculate is attained at about 25 months.     

Effect of average litter weight in pigs on growth performance,carcass characteristics and meat quality of the offspring as depending on birth weight

Offspring born from normal litter size (10 to 15 piglets) but classified as having lower than average birth weight (average of the sow herd used: 1.46 ± 0.2 kg; mean ± s.d.) carry at birth negative phenotypic traits normally associated with intrauterine growth restriction, such as brain-sparing and impaired myofiber hyperplasia. The objective of the study was to assess long-term effects of intrauterine crowding by comparing postnatal performance, carcass characteristics and pork quality of offspring born from litters with higher (>1.7 kg) or lower (<1.3 kg) than average litter birth weight. From a population of multiparous Swiss Large White sows (parity 2 to 6), 16 litters with high (H = 1.75 kg) or low (L = 1.26 kg) average litter birth weight were selected. At farrowing, two female pigs and two castrated pigs were chosen from each litter: from the H-litters those with the intermediate (H_I = 1.79 kg) and lowest (H_L = 1.40 kg) birth weight, and from L-litters those with the highest (L_H = 1.49 kg) and intermediate (L_I = 1.26 kg) birth weight. Average birth weight of the selected H_I and L_I piglets differed (P < 0.05), whereas birth weight of the H_L- and L_H-piglets were similar (P > 0.05). These pigs were fattened in group pen and slaughtered at 165 days of age. Pre-weaning performance of the litters and growth performance, carcass and meat quality traits of the selected pigs were assessed. Number of stillborn and pig mortality were greater (P < 0.05) in L- than in H-litters. Consequently, fewer (P < 0.05) piglets were weaned and average litter weaning weight decreased by 38% (P < 0.05). The selected pigs of the L-litters displayed catch-up growth during the starter and grower–finisher periods, leading to similar (P > 0.05) slaughter weight at 165 days of age. However, H_L-gilts were more feed efficient and had leaner carcasses than H_I-, L_H- and L_I-pigs (birth weight class × gender interaction P < 0.05). Meat quality traits were mostly similar between groups. The marked between-litter birth weight variation observed in normal size litters had therefore no evident negative impact on growth potential and quality of pigs from the lower birth weight group.     

Effect of litter birth weight standardization before first suckling on colostrum intake,passive immunization,pre-weaning survival,and growth of the piglets

Within-litter variation in birth weight is a relevant factor in pig production. This study aimed at comparing pre-weaning mortality, colostrum intake (CI), passive immunization, and growth of piglets from litters of uniform (UN) or heterogeneous (HET) birth weights. The study included 52 multiparous sows (Large White × Landrace) and their litters. Two types of litters were constituted based on birth weight, namely: UN or HET, the control group, using piglets from two to three sows farrowing approximately at the same time. At birth, piglets were weighed, identified, and placed in a box under an IR lamp. At the end of farrowing, piglets were re-weighed and allotted to groups UN or HET (12 per litter) with average weights of 1 394 and 1 390 g, respectively, and allowed to suckle (time 0). They were re-weighed 24 h later to estimate CI and sows' colostrum yield. At time 0, the average intra-litter CV (%) in weight of experimental litters were 9.3 ± 0.8 (SEM) and 27.8 ± 0.7 in groups UN and HET, respectively (P < 0.001). At 2 days of age, blood samples were taken from the piglets of 11 litters five UN and six HET) and serum Immunoglobulin G (IgG) contents were determined. Mean CI/piglet/litter was similar in both groups, that is, 415 ± 13 in UN and 395 ± 13 g in HET (P = 0.28), but was less variable in UN litters (CV = 22.4 ± 2 vs 36.0 ± 2%, P < 0.001). The IgG levels at 2 days of age were higher in piglets from UN litters (22.5 ± 0.8 vs 18.4 ± 0.7 g/l; P < 0.001) but the CV of IgG levels was not different between litter type (P = 0.46). Mortality up to 21 days of age was lower in UN litters (6.4 vs 11.9%, P = 0.03). The BW at 21 days was not different between litter type (P = 0.25) but it was less variable among piglets from UN litters (CV: 17.1 ± 1.3 vs 25.7 ± 1.3%; P = 0.01). Results reveal that CI is less variable and mortality is lower in piglets from litters of UN birth weight. The results infer that genetic improvement to decrease variation in birth weight within-litter could have a positive effect on homogeneous CI and thus contribute to reducing piglet mortality.     

Some aspects related to conception of the Japanese monkey (Macaca fuscata)

The season of birth, age of the first parturition, gestation period, and vaginal bleeding and mating after conception were surveyed with Japanese monkeys (Macaca fuscata). The analyses of the former two items were dependent on the birth records in the Ohirayama troop collected from 1957 to 1973, and the analyses of the latter two items were dependent on data obtained by a 48-hour mating in a laboratory. Birth in the Ohirayama troop converged into the months from March to July, especially from April to June. The age of the first parturition was three years and 11 months at the earliest, and nine years and two months at the latest. The monkeys giving their first birth at the age of five or thereabouts were most frequently observed (68.6%), and most of the monkeys had their first parturition from about the age of four years to about the age of six years. The gestation period calculated from 17 cases, which was defined as the period from the first day of a 48-hour mating to the day before parturition, was 173 ± 6.9 days ranging from 161 to 188 days. In 25 out of 28 cases, the vaginal bleeding was observed after conception. It began slightly later (between 16 and 24 days after mating) than the forecasted time of the next menstrual hemorrhage, and usually lasted longer than bleeding of the usual menses. Each of three female monkeys caged together with a male monkey 30 days after conception was observed to have copulated, and the male was observed to have ejaculated.     

The age of puberty of the hippopotamus (Hippopotamus amphibius Linn.) in the Luangwa River in eastern Zambia

As part of a study of the ecology of a high density hippopotamus population (Hippopotamus amphibius) in the Luangwa river in eastern Zambia, a shot sample of 176 males and 161 females was examined. All animals were classified according to age (0–43 years). The female reproductive organs were removed, dissected, examined, and the lactational status was noted. Ovaries and corpora Iutea were weighed, sliced, and all follicles > 5 mm in diameter were recorded. The testes of the males were dissected and weighed. Indications of puberty and maturity in the female were observed in some animals at an age of about 7 and 8 years respectively; but some animals were still not breeding until 20 years of age and the ages at which 50% of the female population reached puberty and maturity (Laws & Clough, 1966) were 11 and 13 years respectively. In the male, puberty begins at an average age of 6 years and maturity is reached at approximately 8 years of age. The data showed that lactation has no effect on ovarian weight or activity. The weight of the corpus luteum during pregnancy (36–72 ± 2–65 g) is significantly (P < 0–01) greater than that observed in non-pregnant animals (16–64 ± 2–46 g). Multiple ovulation occurs in 8–10% of the animals.     

Birth weight is inversely associated with central adipose tissue in healthy children and adolescents

Objective: Previous studies have explored the association between birth weight and excess childhood body fat, but few have used precise measures of body composition, leading to equivocal and sometimes contradictory results. Research Methods and Procedures: Subjects included 101 children who underwent DXA measurements between 1995 and 2000. Birth weight and gestational age were assessed using maternal recall. Multiple linear regression analysis was used to determine the relationship between birth weight and the following four outcome variables: total fat mass (FM), truncal fat mass (TrFM), percentage body fat (%BF), and TrFM adjusted for FM (TrFMadj), controlling for current weight and Tanner stage. Results: The mean age of the children studied was 12.9 ± 2.4 years, and the mean birth weight reported by subjects’ mothers was 3.3 ± 0.5 kg. The FM and TrFM were 12.8 ± 8.7 kg and 5.1 ± 4.1 kg, respectively, and the mean %BF was 22.9 ± 10.3%. Birth weight was a significant predictor of FM (p = 0.02) and %BF (p = 0.038). However, birth weight adjusted for gestational age (BWTadj) was a significant (p = 0.03) negative predictor of TrFMadj, independently of race, sex, Tanner stage, and current weight. Discussion: These results provide evidence that, even in childhood and adolescence, a higher birth weight is associated with higher FM and %BF, while a low birth weight is associated with TrFM, adjusted for FM.