Rule of age and size at maturity: individual variation in the maturation history of resident white-spotted charr

Individual growth and maturation histories, age, and size at maturity of resident white-spotted charr Salvelinus leucomaenis were examined in a tag-recapture study in a natural river over 3 years. Slow-growing fish reached sexual maturity not only at an older age, but also at a smaller size than fast-growing fish, although females had a larger threshold size at maturity than males at each age. It is suggested that these patterns result from adaptive phenotypic plasticity that depends on individual growth conditions.     

Body size and the adoption of a migratory tactic in brook charr

The presence of a conditional strategy based on size attained before migration and a sex-ratio at migration biased towards females were explored in a population of brook charr Salvelinus fontinalis in the Sainte-Marguerite River, Quebec Province, Canada, where anadromous and resident forms live sympatrically. Seaward migration in the system occurred at 1 and 2 years old. Comparisons between backcalculated size-at-age of migrant and resident fish revealed that smaller fish at age 1 year delay migration to the following year and that bigger fish either migrated at age 1 year or remained resident for the rest of their life-cycle. Slow growth was associated with migration later in life (age 2 years) at a bigger size, which is consistent with the hypothesis of a threshold size for migration. No difference in size at age 1 year between migrant and resident fish suggests that other factors, such as growth efficiency and the presence of heritability of the tactics, are involved. Overall the sex ratio was equal for migrant and resident fish, while an age-specific bias was found: more males migrated at age 1 year and more females at age 2 years. These differences suggest that different tactics are adopted by different sexes.     

Graphical analysis of the life history evolution of Oenothera glazioviana Micheli

Summary Five-year census data of a semelparous Oenothera glazioviana population in a sand dune system were graphically analyzed. Changes in survivorship until seed production and potential fecundity were calculated from the size-dependent growth, survival and reproduction. The net reproductive rates after logarithmic transformation were plotted against the presumed age of reproduction. The optimal age and size at reproduction that maximize the intrinsic rate of natural increase were determined as a gradient of the tangent drawn from the origin. The natural population reproduced a little earlier than the calculated optimal age but at nearly the optimal size. Examination of the effect of environment on the optimal age and size revealed that an environment imposing higher mortality increases both the optimal age and size, while an environment imposing lower fecundity increases the optimal age but not the optimal size. The relatively large critical size for reproduction of O. glazioviana causes delayed reproduction in infertile environments, which helps the species maintain itself in a risky environment such as the sand dunes.     

Reproductive biology and implications for management of the orange-spotted grouper Epinephelus coioides in the southern Arabian Gulf

The reproductive biology of Epinephelus coioides was determined from the examination of 1455 individuals collected between July 2005 and June 2007 in the southern Arabian Gulf. Histological preparations of gonads indicated that males were either derived from a juvenile phase or the transition of postspawning females, confirming a diandric protogynous sexual pattern. The spawning season was well defined, occurring once a year during April and early May. Peaks in spawning occurred after the full and new moons and was completed within a single lunar cycle. The presence of mature males over the entire size and age range and the absence of inactive mature females during the spawning season suggested that the population was not constrained by sperm limitation. While specimens undergoing sexual transition were only observed in size and age ranges of 335–685 mm total length ( L _T) and 5–6 years, patterns in the proportion of males in size and age classes suggested that sex change occurred at a relatively constant rate after female maturation up to the maximum size (1002 mm L _T) and age (11 years). Relationships between reproductive output and capacity with size and age indicated that conventional regulations that equate the mean size at first capture to sexual maturation are unsuitable for the management of E. coioides . The maximum age, small size and young age at sexual maturation ( L _min= 320 mm L _T, 2 years, for females and 242 mm L _T, 1 year, for males) conflict with the general pattern for large epinepheline groupers and may be a direct result of the intensive demersal fishery in the southern Arabian Gulf.     

Fitness consequences of the timing of metamorphosis in a freshwater crustacean

Metamorphosis is a common life-cycle transition in organisms as diverse as amphibians, insects, fishes and crustaceans, and the timing of this transition often affects an individual's fitness. Here, we measured age and size at metamorphosis in laboratory-reared individuals of the freshwater copepod, Diaptomus leptopus , and then followed individuals over their entire life cycle to assess the fitness consequences of variation in age and size at metamorphosis. In 3 separate experiments, individuals were raised in different food conditions: low food (0.2 μg C/ml) switched to high food (0.7 μg C/ml), or high food switched to low food, at several different larval and juvenile stages. Control individuals were reared on high or low food concentrations over their entire life cycles. For each individual, we measured age and size at metamorphosis and age and size at maturity; for females, we also measured total lifetime egg production, longevity, and calculated a composite fitness measure, λ. Statistical analyses showed no significant effects of age or size at metamorphosis on these same traits measured at maturity, or on the fitness components we estimated. The first individuals to mature had the highest total egg production and individual fitness; differences in body size at maturation explained none of the variation observed in fitness components. Our results show that metamorphosis was uncoupled from maturity and from fitness components by growth and development achieved during the juvenile phase of the life cycle, and support the conclusion that fitness consequences of metamorphosis depend fundamentally on the organization of an organism's life cycle. They also suggest that body size plays a different life-history role in these organisms than is recognized in most poikilotherms, and suggest the hypothesis, based on laboratory experiments, that selection may act primarily on juvenile developmental rates in field populations.     

Variation in age at first reproduction of male Japanese fluvial sculpin induced by the timing of parental reproduction

The relationships between age and size at reproduction and lifetime reproductive output of male Japanese fluvial sculpin Cottus pollux were estimated by a mark-recapture study. Although all males were physiologically capable of breeding at age 2 years, age at first successful reproduction varied amongst individuals. Males with delayed reproduction had lower net reproductive rate than males that bred at age 2 years on average suggesting that age at first reproduction was a conditional strategy. Males that delayed reproduction were significantly smaller at age 1 and 2 years than males that bred at age 2 years. Despite no significant difference in body size of hatched yolk-sac larvae between the early and late phase of the breeding season, by May of the first year of life, progeny from nests in the early phase had hatched earlier and were larger than those from the nests in the late phase. The results suggested an important effect of timing of reproduction of parents on the growth and subsequent age at first reproduction of their progeny.     

Genetic study of the height and weight process during infancy.

Longitudinal height and weight data from 4649 Dutch twin pairs between birth and 2.5 years of age were analyzed. The data were first summarized into parameters of a polynomial of degree 4 by a mixed-effects procedure. Next, the variation and covariation in the parameters of the growth curve (size at one year of age, growth velocity, deceleration of growth, rate of change in deceleration [i.e., jerk] and rate of change in jerk [i.e., snap]) were decomposed into genetic and nongenetic sources. Additionally, the variation in the estimated size at birth and at 2 years of age interpolated from the polynomial was decomposed into genetic and nongenetic components. Variation in growth was best characterized by a genetic model which included additive genetic, common environmental and specific environmental influences, plus effects of gestational age. The effect of gestational age was largest for size at birth, explaining 39% of the variance. The differences between monozygotic and dizygotic twin correlations were largest for size at 1 and 2 years of age and growth velocity of weight, which suggests that these parameters are more influenced by heritability than size at birth, deceleration and jerk. The percentage of variance explained by additive genetic influences for height at 2 years of age was 52% for females and 58% for males. For weight at 2 years of age, heritability was approximately 58% for both sexes. Variation in snap height for males was also mainly influenced by additive genetic factors, while snap for females was influenced by both additive genetic and common environmental factors. The correlations for the additive genetic and common environmental factors for deceleration and snap are large, indicating that these parameters are almost entirely under control of the same additive genetic and common environmental factors. Female jerk and snap, and also female height at birth and height at 2 years of age, are mostly under control of the same additive genetic factor.     

Reproductive biology and implications for management of the painted sweetlips Diagramma pictum in the southern Arabian Gulf

The reproductive biology of the painted sweetlips Diagramma pictum was determined from 487 individuals collected between January and December 2010 in the southern Arabian Gulf. There was no evidence of sex change and the combination of histological results with the sex composition of the size and age structures indicated a gonochoristic sexual pattern. There were peaks in gonado-somatic indices for females in March and October with spawning occurring during two seasons (April to May and November). The mean size and age at sexual maturity (L(m50) and A(m50) ) were 35·7 cm fork length (L(F) ) and 2·9 years for females and 26·7 cm L(F) and 0·5 years for males. The maximum recorded age (11 years) and small mean size and young age at sexual maturity for males may be a direct result of intensive demersal fishing in the southern Arabian Gulf. There was an exponential increase in the cumulative reproductive potential with size and a linear increase with age for both sexes. The mean L(F) (L(c50) ) at which D. pictum became vulnerable to capture was 33·3 cm, which corresponded to only 3 and 7% of the cumulative reproductive potential of males and females, respectively. Size-specific and age-specific reproductive potential indicated that conventional regulations that equate the mean size at first capture to sexual maturation are unsuitable for the management of D. pictum.     

Reproductive biology and implications for management of the spangled emperor Lethrinus nebulosus in the southern Arabian Gulf

The reproductive biology of the spangled emperor Lethrinus nebulosus in the southern Arabian Gulf was determined from the examination of 781 individuals collected between September 2008 and August 2009. There was no histological evidence of adult sex change, and sex ratios did not differ significantly from unity across all size and age classes. Testes had an ovarian structure and a remnant lumen which was not used for sperm transport; furthermore, residual oocytes were observed in the testes of some immature, resting and developing males. A dramatic change in the sex ratio of the smallest and youngest size and age classes suggested that juvenile female to male sex change occurred between 21·0 cm fork length (L(F)) and 24·0 cm L(F) at 1 year of age. The combination of histological evidence with the sexual composition of the size and age structures suggests a non-functional protogynous hermaphroditic sexual pattern, which is analogous to functional gonochorism. The spawning season was well defined, occurring once a year during March, April and early May. Peaks in spawning occurred after full moons, there was a cessation in spawning activity after new moons and spawning was completed within three lunar cycles. The distribution of males over the entire size and age ranges and the absence of inactive mature females during the spawning season suggested that the population was not constrained by sperm limitation. Size-specific and age-specific reproductive potential indicated that conventional regulations that equate the mean size at first capture to sexual maturation are unsuitable for the management of L. nebulosus. The maximum recorded age (11 years), small mean size and young age at sexual maturation (L(m50) = 26·7 cm L(F), 2·1 years, for females and 19·4 cm L(F), 0·5 years, for males) may be a direct result of intensive demersal fishing in the southern Arabian Gulf.     

Retardation of bone development in the Koshima troop of Japanese macaques

Retardation of bone development was observed in the Koshima troop of free ranging Japanese macaques. In the control group, epiphyseal unions of appendicular long bones generally started to close at about 4 yrs of age and were completed at about 8 or 9 yrs of age. Limb bone unions of the Koshima troop, however, started to close at about 9 yrs of age and completely closed at about 15 yrs of age. In the epiphyseal unions of trunk and girdle bones, the Koshima troop again showed a retardation of closure compared with the control group. Until long bones reached their full length, that is, until about 15 yrs of age, their size was small in the Koshima troop compared with the control group, though the sample size of the Koshima troop was small. After 15 yrs of age, however, many osteometrical measurements of the Koshima troop were nearly the same as controls. A prolonged growing duration compensated for the slow growth and allowed them to become as large as controls. This prolongation may be an adaptation in response to small size during the developmental period. In some parts of the body, however, Koshima macaques failed to reach the adult size of controls. Males were less likely than females to reach full size. Causes of the retardation and small size in the Koshima troop are discussed, but they remain open to further studies.     

Changes in size and age at maturity in a population of kokanee Oncorhynchus nerka during a period of declining growth conditions

Trends in size distributions and age at maturity of spawning kokanee Oncorhynchus nerka during a 5 year period of declining growth conditions at Bucks Lake, California, U.S.A. were consistent with the hypothesis that reductions in growth rates in successive cohorts induce a shift to an older age at maturity. This forestalls decreases in size at maturity during a transitional period characterized by an increasing proportion of individuals that delay maturation. During the course of the study, kokanee first began declining in size at maturity, and then shifted from a 3 year to a 4 year egg to adult cycle. Individuals that spawned during their fourth year (age 3 years) were significantly larger, on average, than members of their cohort that spawned during their third year (age 2 years). This difference was greatest when age 2 year adults were smallest. The shift to an older age at maturity prevented a steady decline in size at maturity, even though age‐specific size was steadily declining over time. Size at maturity, however, began to decline again once the transition to a 4 year cycle was complete. In addition, there was a general trend of decreasing length‐specific mass. The data indicate that there is a range of growth trajectories over which delayed maturity can prevent a temporal pattern of decreasing size at maturity as growth rates decline.     

Alternative life histories in Xiphophorus multilineatus: evidence for different ages at sexual maturity and growth responses in the wild

In order to examine potential trade-offs in alternative life histories of the high-backed pygmy swordtail Xiphophorus multilineatus, otoliths were used from wild-caught males to determine if sneaker males had the advantage of maturing earlier in natural environments. The sneakers matured significantly earlier than courters, but there was no difference among the three courter variants. In addition, analyses suggested that the effect of the pituitary locus on size at sexual maturity and growth rates was a consequence of age at sexual maturity. Finally, one of the courter variants had a significantly different relationship between age and size at sexual maturity than the other variants, suggesting that in this variant, age at sexual maturity may be more closely related to size and therefore may be less plastic in its growth responses.     

Developmental thresholds and the evolution of reaction norms for age and size at life-history transitions

It is quite common in studies of life-history plasticity to find a negative relationship between the age at which various life-history transitions occur and the growth conditions under which individuals develop. In particular, high growth typically results in earlier transitions, often at a larger size. Here, we use a relatively general optimization model for age and size at life-history transitions to argue that current life-history theory cannot adequately explain these results. Specifically, most such theory requires key assumptions that are unlikely to be generally met. This suggests that some important component of the biology of many organisms must be missing from many of the models in life-history theory. We suggest that this missing component might be the phenomenon of developmental thresholds. There are at least two different types of developmental thresholds possible, and we incorporate these into our general optimality model to demonstrate how they can cause a negative relationship between growth conditions and age at a transition. If developmental thresholds are common throughout taxa, then this might explain the empirical results. Our model formulation and analysis also formalizes the popular Wilbur-Collins hypothesis for age and size at metamorphosis in amphibians. The results demonstrate that optimal combinations of age and size, and the slope of the reaction norm connecting them, depend on the existence and type of threshold assumed. Our results also provide an evolutionary framework that can be used to view the data and many of the proximate submodels derived from the Wilbur-Collins hypothesis.     

Body size, age and reproduction in the Smooth newt, Triturus vulgaris

Data on the relationships between individual body size, age and reproduction were obtained for a sample of Smooth newts collected from several sites in southern England. Age was determined by counting lines of arrested growth in histological sections of humerus. In males and females, body size increases with age, but only in the former sex is the correlation statistically significant. In both sexes, there is great inter-individual variability in body size within a year class. Measures of fecundity (testis size, ovary size, clutch size and oocyte size) are positively correlated with body size, but not age. The timing of first reproduction does not seem to depend on the attainment of a fixed body size; the earliest age at first reproduction is two or three years. Together with information obtained during previous studies, the data we present support the hypothesis that the Smooth newt may be an r -selected, colonizing species.     

Maturation patterns in female European eel: age and size at the silver eel stage

The maturation pattern in the female European eel Anguilla anguilla was studied by investigating age and size patterns of silver eels in different aquatic environments in Sweden, covering limnic, brackish and marine waters. The results neither supported the hypothesis that there is a critical size or age when eels enter the silvery stage, nor that size and age at maturity are positively related. Age at maturity, however, was observed to be negatively related to growth rate in all localities, i.e. the female reproductive tactic apparently is to become sexually mature at the earliest possible opportunity. Furthermore, it was recognized that a significant amount of variation was due to habitat differences, since the female eel maturation pattern deviated systematically between sampling sites, as it did also when the effect of growth rate was eliminated. Thus, the ability of the female eel to adjust maturation to an optimal size and age can be questioned, because the panmictic nature of the eel means local adaptations are unlikely Growth rate dependent differences suggest that variations in maturation patterns between eel environments are linked more to the opportunity for nutrient accumulation than to other aspects of growth.     

Influences of prenatal and postnatal fraternity size on ovarian development in the mouse

An experiment was conducted to test effects of prenatal and postnatal fraternity size (size of litter in which an individual develops prenatally or is reared postnatally) on ovarian development in mice. Fraternity size treatments were created by standardizing sizes of prenatal and postnatal fraternities in which mice were gestated and reared. Prenatal fraternity size was standardized by surgery on Day 9 of gestation to 6, 10, and 14 fetuses. Postnatal fraternity size was standardized by randomly assigning pups to litters of 5, 10, or 15 pups within 24 h of birth. Female pups were killed at either 3 or 20 wk of age and right ovaries were prepared for histology. Follicles were classified by size and morphology, and numbers of follicles in each class were tabulated. Interaction of postnatal fraternity size and age was observed for number of antral follicles (p less than 0.05). Mice reared in small postnatal fraternities had more antral follicles at weaning (3 wk) and fewer antral follicles at maturity (20 wk of age) than mice reared in large postnatal fraternities. No effect of either prenatal or postnatal fraternity size on other follicle populations was observed (p greater than 0.20). Numbers of Type 2 (primordial), Type 3a, and Type 3b follicles changed with age (p less than 0.01); numbers of primordial follicles declined with age, but numbers of Type 3a and 3b follicles increased. A hypothesis of a negative association between postnatal fraternity size and number of antral follicles at 3 wk of age was supported, but a hypothesis of a positive association between fraternity size and number of primordial follicles was not supported.     

Phenotypic variation in metamorphosis in four species of freshwater copepods

1. Physiological metamorphosis accompanied by an ecological habitat shift is a widespread life-history phenomenon, and both age and size at metamorphosis are highly variable in many organisms. In this study, age and size at metamorphosis (defined as the transition from the last naupliar to the first copepodite stage) were quantified for four species of freshwater copepods to determine the scale on which these two traits vary, if age and size at metamorphosis are equally variable, and if variation at metamorphosis is related to variation in newborn size. 2. Measurements of laboratory-reared and field-caught individuals show that age and size at metamorphosis, together with newborn size, vary among siblings, between families within a population, between populations of one species and between closely related species. 3. In all populations, age at metamorphosis was the most variable trait, a result observed in many other organisms. Most of the variation in age at metamorphosis could be explained by differences between families within a population, while differences among siblings from the same clutch accounted for most of the variation in size at metamorphosis. 4. Although newborn size was variable, differences in this trait could not fully account for variation observed at metamorphosis. Newborn size differed among populations, but most interpopularional differences disappeared by the rime metamorphosis was reached. In particular, size at metamorphosis appears to be tightly constrained in freshwater copepods. 5. Age and size at metamorphosis were not equally variable among species, either. Species-specific metamorphic envelopes (joint distributions of age and size at metamorphosis) result from differences in trait means, variances and covariances, and suggest very different larval growth trajectories among three of the species examined.     

Effect of resource gradient on age and size at maturity and their influence on early‐life fecundity in the predatory Asian lady beetle,Harmonia axyridis

Variation in food availability impacts the performance of insects in terms of their size and age to maturity and fecundity. Age at maturity determines how quickly individuals in a population can start to reproduce and how much they can reproduce. Results from studies on various insect species show that food availability influences the size and fecundity of adult females. It is predicted that under poor growth conditions, variation in size is low, but variation in age at maturity is considerable. This prediction was examined in a widely distributed lady beetle species, Harmonia axyridis (Pallas) (Coleoptera: Coccinellidae), a predator of aphids and coccids. Using a food gradient from low to high aphid prey density, performance of females that were reared on excess food was recorded for pre‐reproductive duration, size at reproductive maturity, number of aphids consumed, and fecundity in the first 10 days of their reproductive period. Results suggested that female H. axyridis that were reared on surplus food when kept at low prey density (poor growth condition) took, on average, three times longer to attain maturity and produced, on average, 14 times fewer eggs than females that were also reared on surplus food, but kept at high prey density (good growth condition). Females performed best at a prey density of 30 aphids per female per 150 cm². Results suggested that the current food availability significantly influenced the age and size of females at maturity and their fecundity. Age and size at maturity of female lady beetles showed non‐linear responses to prey density as well as the occurrence of a minimum size of females, below which H. axyridis females fail to mature. The steep slope recorded at lower prey densities suggests relatively high variation in age at maturity but low variation in size.     

Correlated contemporary evolution of life history traits in New Zealand Chinook salmon, Oncorhynchus tshawytscha

Size at age and age at maturity are important life history traits, affecting individual fitness and population demography. In salmon and other organisms, size and growth rate are commonly considered cues for maturation and thus age at maturity may or may not evolve independently of these features. Recent concerns surrounding the potential phenotypic and demographic responses of populations facing anthropogenic disturbances, such as climate change and harvest, place a premium on understanding the evolutionary genetic basis for evolution in size at age and age at maturity. In this study, we present the findings from a set of common-garden rearing experiments that empirically assess the heritable basis of phenotypic divergence in size at age and age at maturity in Chinook salmon (Oncorhynchus tshawytscha) populations introduced to New Zealand. We found consistent evidence of heritable differences among populations in both size at age and age at maturity, often corresponding to patterns observed in the wild. Populations diverged in size and growth profiles, even when accounting for eventual age at maturation. By contrast, most, but not all, cases of divergence in age at maturity were driven by the differences in size or growth rate rather than differences in the threshold relationship linking growth rate and probability of maturation. These findings help us understand how life histories may evolve through trait interactions in populations exposed to natural and anthropogenic disturbances, and how we might best detect such evolution.     

Phenotypic plasticity in age and size at maturity and its effects on the integrated phenotypic expressions of life history traits of Cardamine flexuosa (Cruciferae)

We analyzed variation in phenotypic plasticity of life history traits between two Cardamine flexuosa populations based on differences in plasticity of age and size at maturity. C. flexuosa (Cruciferae) is a facultative, vernalization-sensitive, long-day annual, and its phenology and the phenotypic expressions of many life history traits are largely controlled by photoperiod and vernalization in natural populations. We used plants from two populations which differed in their responses to chilling and photoperiod treatments. The timing of developmental processes was changed by controlling temperature and photoperiod regimes in growth chambers. Plasticity in size at maturity was analyzed as changes in a growth trajectory using two parameters, age at maturity (Δt) and growth rate (k). Both traits showed plasticity, but differences between the populations were found mostly for Δt. Distinctive differences in size at maturity of individuals in the two populations were mainly due to different amounts of plasticity in Δt. Variations in plasticity of nine other life history traits and their associations to age and size at maturity were also analyzed. Variation for eight of the traits can be described, at least in part, as a function of age and size at maturity for both populations, and most of the variation in the total number of seeds was explained by age and size at maturity. Only age at maturity had any effect on changes in resource allocation. The nine life history traits were integrated through associated character expressions with age and size at maturity. Changes in the association between a trait and age and/or size at maturity were rather conservative compared to changes in the plasticity of a trait between the two populations. Associations with age and size at maturity are mostly explicable in terms of inherent relationships in the developmental processes, and they may limit the ecological range expansion and the adaptive evolution of plasticity in C. flexuosa. The negative correlation between reproductive allocation and age at maturity can be a cost of delaying maturation in C. flexuosa.