Effects of sexual differences of age at maturity and survival on population sex ratio

Summary Five demographical factors influencing the sex ratio of a population are classically considered. The influence of two of them is dependent on the longevity of individuals in the population. The effect of differential age at maturity between males and females is higher for animals with low annual survival, whereas the effect of differential annual survival between males and females is higher for animals with high annual survival. Such a conclusion applied to turtles, which are long life-span animals, allows us to retain differential survival between sexes as a major factor influencing the population sex ratio.     

Optimal age at sexual maturity of sympatric and experimentally allopatric cutthroat trout and Dolly Varden charr

Summary Reproductive potentials of transplanted curthroat trout (Salmo clarki) and Dolly Varden charr (Salvelinus malma) and of their donor stocks were estimated from life history data. We found good agreement between observed and predicted age at maturity in all populations, and cannot reject the hypothesis that the fish matured at the age maximizing the overall lifetime reproductive potential ( ). Our estimates were insensitive to probable variations in female fecundity, adult mortalityrate and maximum body length. Small changes in either juvenile mortality-rate or individual growth-rate had marked effects on the estimations, as did changes in the Malthusian parameter (r). Three alternative mechanistic explanations of how age at maturity is determined could be rejected. We suggest that fish are able to adjust the maturity age non-genetically to changes in growth-rate, and that temporal variations in juvenile survival-rate allow coexistence of genotypes coding for different ages at maturity at the same growth-rate.     

Growth and age at sexual maturity of South American sea lions

The average age at sexual maturity (ASM) is an important parameter for evaluating the reproductive potential or status of a population. South American sea lions, Otaria flavescens in Patagonia (Argentina) were exploited and reduced to less than 10% of pre-exploitation numbers. At present, the population is recovering at a rate of 6%. In this paper, we studied growth and age at sexual maturity of South American sea lions in the south-western south Atlantic by examining 219 individuals (females and males) collected between 1989-2008. Individuals were aged by counting growth layer groups in tooth sections, standard body length was measured and male and female reproductive organs were examined macroscopically and histologically to establish individual sexual maturity. Maximum recorded length for males and females was 264 cm and 200 cm, respectively, and maximum ages 19 and 21 yrs. ASM defined as the age where 50% of females are mature, was estimated at 4.8±0.5 years old, corresponding to a mean SL of 147 cm, about 81% of their asymptotic length. First observed ovulation occurred during the 4th year, first birth may occur between 4 and 5 years old. Males physiologically mature between 4-6 years, but the size of the testes shows that all males became sexually mature by the age of 9 years when they reach a mean SL of 212 cm, about 86% of their asymptotic body length. The present information on ASM and growth of O. flavescens will improve the development of population dynamics models, to investigate the impact of recovering sea lions populations on its marine environment, as well as its trophic interactions with commercial fisheries.     

Reassessment of age of sexual maturity in gibbons (hylobates spp.)

From studies of both wild and captive animals, gibbons are thought to reach sexual maturity at about 6 to 8 years of age, and the siamang (Hylobates syndactylus) at about 8 to 9 years. However, a review of the literature reveals that in most cases the exact age of the maturing animals was not known and had to be estimated. This study presents seven case reports on captive gibbons of known age. Captive males of the white-cheeked crested gibbon (H. leucogenys leucogenys) and of the siamang (H. syndactylus) can breed at the age of 4 and 4.3 years, respectively. Similarly, hybrid females (H. lar × H. moloch) and siamang females can breed at 5.1 and 5.2 years, respectively. This finding may help to improve the breeding success of captive gibbon populations. It is not clear whether gibbons reach sexual maturity earlier in captivity or whether sexual maturity is also reached by 5 years of age in the wild. Possible implications for the interpretation of group size regulation and of reproductive strategies of wild gibbons are discussed.     

Body mass, age and sexual maturity in short-beaked echidnas, Tachyglossus aculeatus

During the course of this 12 year field study body masses of 11 hatchling echidnas (Tachyglossus aculeatus multiaculeatus) and 25 pouch young between the ages of 5 and 60 days were recorded. Body mass increased from 0.3 to approximately 50 g in the first half of pouch life. It then quadrupled before young were placed in a burrow at 45 to 55 days of age. There was a positive correlation between the body mass of the female and that of her young at weaning. From 33 subadult echidnas located, tagged and radio tracked during this study, body masses of 10 were monitored to sexual maturity, i.e. when first encountered in a courtship train. Minimum age of sexual maturity ranged between 5 and 12 years. As subadults, there was no difference between mean body masses of males and females. At sexual maturity, mean body mass of females was significantly higher. No correlation was found between age at sexual maturity and body mass nor was there a significant difference in age of males and females at sexual maturity.     

Father absence predicts age at sexual maturity and reproductive timing in British men

Despite the widespread assumption that paternal investment is substantial in our species, previous studies have shown mixed results in relation to the impact of fathers on both offspring survival and reproductive outcomes. Using data from a large representative sample of British men, we tested whether father absence is associated with the timing of reproduction-related events among boys, while controlling for various cues denoting early childhood adversity. We further tested whether the loss of the father at different childhood stages matters, so as to assess whether early life is the most important period or if effects can be seen during later childhood. The results show that father absence before age seven is associated with early reproduction, while father absence between ages 11 and 16 only is associated with delayed voice-breaking (a proxy for puberty), even after adjusting for other factors denoting childhood adversity. We conclude that fathers do exert an influence on male reproductive outcomes, independently of other childhood adversities and that these effects are sensitive to the timing of father absence.     

Variation in length and age at sexual maturity of Atlantic groundfish: a reply

Synopsis The assertion has been made by Halliday (1987) that trends in size and age at maturity of Atlantic groundfish published by Beacham (1983a, b, c, d, e, f) are artifacts induced by errors in determining the sex of an individual, distinguishing between immature and mature fish, sampling fish outside of the regular spawning season, and by nonrandom sampling of the population. In particular, Halliday asserts that for the Atlantic argentine,Argentina silus analysis, the conclusions of Beacham (1983a) that: (1) median length at sexual maturity declined over time; and (2) males matured at older ages than did females are invalid owing to biases in both sampling and analysis. In fact, if some of the biases indicated by Halliday were significant, then the decline in median length at sexual maturity is enhanced and the conclusions of Beacham (1983a) reinforced. Size and age at sexual maturity are dynamic characters in many vertebrate populations, and the fact that they should change for Atlantic groundfish should not be surprising given variable exploitation patterns in the fisheries since 1960.     

Optimal age and size at maturity in annuals and perennials with determinate growth

Summary A model predicting optimal age and size at maturity is presented, exploring the conflict between growth and energy allocation to reproduction. According to the model, the factors promoting delayed maturity and large adult body size are as follows: (1) high rate of somatic growth, (2) high percentage increase in reproductive rate with body size increase, (3) long life expectancy at maturity for annuals or large number of expected productive days (when either growth or reproduction is possible) for perennials with growth ceasing at maturity, (4) life expectancy increasing with body size. All these factors are combined in the mathematical formula predicting optimal age and size at maturity, which allows for quantitative predictions. The optimal schedule of growth and reproduction may be achieved by natural selection, developmental plasticity, or when one species replaces another. Sexual size dimorphism is also discussed, resulting from different optimal age at maturity for either sex.     

Light intensity and sexual maturity

There are confirmable clines, by latitude, of melanin concentration in pigmentation for man as well as other mammals and birds. This has been suggested to be, in man, a result of the importance of vitamin D synthesis which can be inhibited by darker skins in higher latitudes. Experiments on mice suggest that another mechanism may be operative; greater photic stimulation of the pineal lowers the age at first estrus and may confer a reproductive advantage in this way.     

Influence of sexual maturity of donor on in vivo survival of transferred porcine embryos.

A study was conducted to determine whether embryos recovered from first-estrous (pubertal) and second-estrous gilts differed in survival when transferred to first- or third-estrous recipients. Embryos were recovered surgically from first- and second-estrous donors 48-72 h postmating and 6-10 normal embryos/zygotes (1-4 cells) were transferred to oviducts (3-5 embryos/ampulla) of nonmated synchronous first- (n = 40) or third- (n = 15) estrous recipients. Blood samples were collected from the jugular vein of recipient gilts on Days 3, 12, and 30 of gestation and the sera were analyzed for progesterone and free (unconjugated) estrogens by use of radioimmunoassays. Recipient gilts were subsequently slaughtered between Days 30 and 40 to assess embryonic losses. Mean number of ovulations was lower among first-estrous vs. third-estrous recipients (8.9 +/- 0.7 vs. 11.4 +/- 0.7; p < 0.05). Percentage of recipients that maintained pregnancy was similar between first- and third-estrous gilts (67.5 vs. 60.0%) and recovery of total conceptuses (normal and degenerating) resulting from transfer of one-cell- and cleavage-stage embryos did not differ among first- vs. third-estrous gilts (76.1 vs. 78.2%). Similarly, percentage of viable fetuses in first-estrous gilts that were pregnant from transfer of one-cell- and cleavage-stage embryos was not different from that of third-estrous gilts (69.3 vs. 75.6%). Percentages of total conceptuses and viable fetuses in first- and third-estrous gilts that were recipients of cleavage-stage embryos only also did not differ (p > 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)     

Temporal changes in fecundity and age at sexual maturity of southern elephant seals at Marion Island

Our objective was to examine the effect of variation in reproductive parameters on the demography of southern elephant seals at Marion Island. We used age-specific capture probabilities of breeding females in a Cormack-Jolly-Seber context to derive reproductive rates. We found that age at maturity declined and fecundity rates increased as the population declined, indicating a compensatory response. Fecundity rates ranged from 0.03 to 0.29 among 3-year-olds (mean=0.16), 0.18 to 0.50 in 4-year-olds (mean=0.40), and 0.28 to 0.50 in 5-year-olds (mean=0.45). We think that a relative increase in food availability, concomitant with the population decline, promoted earlier sexual maturity correlated with more rapid growth of juveniles when population abundance was lower. It is suggested that the relative importance of fecundity in population regulation in elephant seals has been underestimated. Moreover, it appears that the onset of sexual maturity may be the first demographic variable to change in response to a change in population density.     

Size and age at sexual maturity of Atlantic argentine,Argentina silus: a critique

Synopsis A recent analysis of size and age at sexual maturity ofArgentina silus on the Scotian Shelf is invalid because field maturity stage data collected during the non-spawning, quiescent stage of the reproductive cycle were unreliable for distinguishing between immature and resting mature stages. Thus two-thirds of the data used must be discounted. Utilization of different length measurement criteria for different years, for which no correction is made, could introduce substantial error in length at maturity estimates based on the remaining data. Age data collections were restricted to one 12 month period and thus were inadequate to characterize age at maturity by 5 yr time periods as attempted in this analysis. No attempt is made in the analysis to determine whether available samples adequately represent the population with regard to maturity i.e. whether immature and mature fish of the same length had an equal probability of being sampled. It is demonstrated here that maturity ogives can differ greatly depending on assumptions made concerning the representativeness of samples. Many of the criticisms made are likely valid for a series of papers on maturity of Atlantic coast fishes by the same author.     

Determination of age, growth and sexual maturity of Barbus grypus in the Dukan reservoir of Iraq

A total of 317 carp Barbus grypus were collected during one year (1977–1978) from the Dukan reservoir of Iraq to study age, grwoth and sexual maturity. The length-weight relationship was found be: log: W =–4.2298 + 2.6832 log L. and the condition ( K ) was 0.88. Back calculation was determined by using a correction factor (45.727) in Lee's equation. Predicted standard length and weight were found to be less than the actual values. The maximum increase in length was noted in the first year group, while the maximum increase in weight occurred at the time of sexual maturity. Males were found to attain maturity earlier than the females. Spawning took place during May and June.     

Growth to sexual maturity of dwarf and nondwarf White Rock chickens divergently selected for juvenile body weight

Summary Growth from hatching to the onset of lay (sexual maturity) was studied in White Plymouth Rock pullets from lines selected for high (HN) and low (LN) 56-day body weight, their reciprocal F₁ crosses, an F₂ cross, and two dwarf populations originating from the HN and LN parental lines. The highest R²s for describing growth for all populations except HN were obtained when body weight was expressed relative to body weight at sexual maturity. Modes of inheritance differed depending on whether patterns of growth were expressed in a chronological time frame or on a physiological basis. Heterosis observed for age at sexual maturity and for body weight after the age when selection was made was not in evidence when ages and weights were expressed as a proportion of those at sexual maturity.This research was supported, in part, by BARD Project No. US-675-83C     

Optimal age of maturity in fluctuating environments under r‐ and K‐selection

Optimality models for evolution of life histories have shown that increased environmental stochasticity promotes early age of maturity. Here we argue that if r‐selection for early maturation implies a tradeoff making those phenotypes more sensitive to a change in population size than phenotypes maturing at older ages, K‐selection can favor delayed onset of maturation. We analyze a general stochastic Leslie‐matrix model with a simplified density regulation affecting all survivals equally through a function of the population vector, often called the ‘critical age class’. We show that the outcome of such an age‐dependent r‐ and K‐selection is that the expected value of the ‘critical age class’ is maximized by evolution, a strategy strongly influenced by the magnitude of the environmental stochasticity. We also demonstrate that evolution caused by such density‐dependent selection influences the population dynamics, showing a possible reciprocal effect between ecology and evolution in age‐structured populations. This modeling approach reveals that changes in population size affecting the fitness of phenotypes with different age of maturity may be an important selective agent for variation in onset of reproduction in fluctuating environments. This provides a testable hypothesis for how patterns in the population dynamics should affect life history variation.     

The peak oxygen uptake of British children with reference to age, sex and sexual maturity

The purposes of this study were to provide baseline data on the peak oxygen consumption (VO2) of British children, aged 11-16 years and to examine the peak VO2 of children in relation to their pubertal stage of development. The peak VO2 of 226 boys and 194 girls was determined during either treadmill running or cycle ergometry. The sexual maturity of 320 of the children was estimated using Tanner's indices. Peak VO2 increased with chronological age in both sexes and from about the age of 12 years boys exhibited significantly higher (P less than 0.05) values than girls. Boys' peak VO2 in relation to body mass was consistent over the age range studied and was superior (P less than 0.05) to girls' values at all ages. It appears that mass-related peak VO2 is independent of sexual maturity in both sexes. The more mature boys demonstrated a significantly higher (P less than 0.05) peak VO2 (1.min-1) than the less mature boys on both ergometers. The more mature girls demonstrated significantly higher (P less than 0.05) peak VO2 (1.min-1) than the less mature girls only on the cycle ergometer. On both ergometers the differences between the peak VO2 of the girls and boys were more pronounced in the mature children whether expressed in relation to body mass or not. Comparison of the results with earlier data drawn from smaller samples failed to provide evidence to suggest that British children's peak VO2 has declined in recent years. No study with which to compare our maturity peak VO2 data appears to be available.     

Ascorbic acid levels in the proglottides of four species of cestode parasites of mammals and birds in relation to their sexual maturity

Ascorbic acid levels were found to be closely related to different stages of growth and maturity of Avitellina centripunctata, Moniezia expansa, and Stilesia globipunctata from goats and sheep and of Raillietina echinobothrida from fowl. The ascorbic acid level in avian parasites was higher than that in mammalian. The level was highest in immature proglottides and lowest in gravid proglottides.     

The relationship between body length, age and sexual maturity in the common toad, Bufo bufo

An investigation of the relationship between the onset of sexual maturity, age and body size in common toads Bufo bufo was started in 1984 at a pond in southern England. During the toad breeding seasons of 1984 and 1985, 7259 common toad'metamorphs'were captured and permanently marked so that if captured as adults their true age would be known. Although a very small proportion of males and females reached sexual maturity at ages of two and four years respectively, most did so much later and asynchronously. The body size of toads breeding for the first time was relatively constant for each sex and not correlated with age. The rational behind our understanding of the mechanism of female choice is discussed in the light of these results.