Determination of growth and maturation in the common frog, Rana temporaria, by skeletochronology

Growth and maturation in a Swiss population of Rana temporaria were studied in 1983 and 1984 by means of skeletochronology. Resting line (growth ring) diameters were used to back-calculate individual body sizes in previous years; these permitted establishment of an average growth curve and determination of individual ages and sizes at first reproduction. Growth was rapid up to maturation, but continued thereafter at a decreased rate. Males were larger than females at age two but females grew faster thereafter, causing sexual dimorphism in adult body sizes. Body size distributions for both years and for frogs recaptured and first captured in 1984 were established. Growth in immatures was positively, but in adults negatively correlated with body size, with considerable variation at all sizes. Individual adult sizes were positively correlated with body sizes at the end of the first year. Average individual age at first reproduction was 2.8 years in males and 3.1 years in females (range in both sexes two to four years). There is no evidence for a two-year-cycle of reproduction.     

The effects of size, age and a cost of early breeding on reproduction in female mountain hares

Both age and size may influence female reproductive performance in mammals, and successful early reproduction may lead to reduced success at later attempts. The effects of age, size and early reproduction on distribution of reproductive effort throughout a single breeding season was examined in female mountains hares Lepus timidus L. Hind foot length was used as an index of body size, because, unlike body weight, it did not fluctuate with reproductive status. Fifty-six female carcasses were collected from March to October 1984, and their litters were assigned to one of three chronologically equal'litter periods'(1–3) of equal length. Whereas number of ova shed was always independent of age, large females shed more ova than did smaller females in litter periods 1 and 2. Prenatal mortality of ova and embryos was highest during litter period 1, when it was independent of age and size. Although prenatal mortality remained high in first year females in litter period 2, there was an overall decline through to the final litter period when it was negligible. Total number of young produced through the season increased with skeletal size in old females (age > 1), but not significantly in first year females. It is concluded that large size, rather than age, favours early reproduction in mountain hares. Every additional offspring produced in litter periods 1 and 2 reduced that female's production in period 3. After correcting for this cost of early reproduction the number of young produced in the final litter period also increased with maternal size.     

Body size, age and reproduction in the leopard toad, Bufo pardalis

Data on the relationships between body size and age were obtained for a sample of leopard toads Bufo pardalis from a breeding population of this species from the Cape Peninsula, South Africa. Age was determined by counting the number of lines of arrested growth in histological sections of a digit clipped from each individual. In males there was a positive, but weak, correlation (explaining only 18% of the variance) between body size and age, and in females no correlation at all existed between these two variables. Males which were successful in obtaining matings were not older than unsuccessful males. Age of males at the breeding site ranged from one to three years, whereas females ranged from two to six years old. This represents both the earliest age of reproduction, as well as the greatest difference in longevity between the sexes, documented for an anuran species.     

Life-history patterns and sociality in canids: Body size,reproduction, and behavior

Summary Empirical associations among co-adapted traits such as body size and patterns of reproduction, development, and behavior are unknown for most animal species, despite numerous theories suggesting otherwise. One way to study these complex relationships is first to consider closely related species and then to generalize findings to other groups. In the present study, relationships among body size, reproductive patterns, development, and sociality were examined in 17 members of the family Canidae (canids). Large canids are more social than smaller species, and offspring of large species achieve independence and tend to breed first at a later age. Large females give birth to absolutely larger young, but relative to their own body weight they allocate fewer resources to bringing a large pup to term. Overall, sexual dimorphism in size is small to moderate, and this is associated with monogamous mating habits and paternal care of young.     

Determinants of age at first reproduction and lifetime breeding success revealed by full paternity assignment in a male ungulate

Age at first reproduction is an important determinant of individual variation in reproductive success in ungulates, but few studies have examined its relationship with later fitness‐related traits in males. We used a long‐term individual based study of a harvested moose population to quantify the individual reproductive performance and survival of males, as well as to examine the determinants of age at first reproduction and consequences of age at first reproduction on lifetime breeding success. The probability that a male successfully reproduced at the age of two was negatively related to the mean age of adult males in the population, but the relationship weakened with increasing population size. Large antlers and large body mass relative to other males in the population increased the number of calves sired at their first successful mating season. In addition, those that successfully reproduced as two year‐olds were more likely to sire calves the next year, making them more productive at a given age compared to those that first reproduced at the age of three or older. We emphasize the importance for males to start reproducing as soon as possible in a harvested population to gain lifetime fitness benefits, as surviving the hunt is a major determinant of reproductive success in this population. We found no costs of early reproduction in males, hence leading to high individual heterogeneity in male reproductive performance. The apparent lack of reproductive costs could partly be explained by the age distribution in the population, individual variation in early‐life body mass and antler size, and differences in probabilities of being hunted of successful and unsuccessful males.     

Do pioneers have r-selected traits? Life history patterns among colonizing terrestrial gastropods

We examine whether pioneer species of terrestrial gastropods (snails and slugs) possess particular life history traits commonly associated with r-selection, using data on gastropod colonization in four areas in north-west Europe (the Kvarken and Tvärminne archipelagos in the Baltic, polder woods in IJsselmeer, and a rehabilitated quarry near Maastricht). Data on age at first reproduction, longevity, clutch size, egg size and lifetime fecundity were gathered from the literature. In order to control for potentially confounding effects of body size on life history traits, we compared the residuals from the allometric relations between life history traits and body size for pioneers and non-pioneers. In snails, all life history traits examined were related to body size. In slugs, all traits except age at first reproduction scaled with body size. Body sizes did not differ between pioneers and non-pioneers in any area. In all four areas, there were no significant differences between pioneers and non-pioneers in any of the life history traits examined, after body size had been taken into account. This indicates that pioneer terrestrial gastropods generally cannot be regarded as r-selected. Pioneer species may possess any of several life history strategies, and the combinations of traits shown by them may have little in common with the r-K selection concept.     

Ontogenetic Shifts in the Ability of the Cladoceran,Moina macrocopa Straus and Ceriodaphnia cornuta Sars to Utilize Ciliated Protists as Food Source

The ontogenetic diet shifts and age specific ability of the two cladoceran species Moina macrocopa and Ceriodaphnia cornuta to derive energy from ciliated protists have been investigated in laboratory. The postembryonic developmental rates and life table demography (longevity, age and size at first reproduction, fecundity and intrinsic rate of natural increase) of the cladocerans have been elucidated on algae (Chlorella vulgaris) and the ciliated protists (Tetrahymena pyriformis, Colpoda (c.f.) steini) as food. For either of the cladoceran, the somatic growth rate and average body size at first reproduction were higher with algal diet. During initial stages of development (0–5 days), either cladoceran realized higher rate of somatic growth on algal diet, subsequently ciliated protists supported significantly higher growth rate than the alga. Algal and ciliate diets did not differ in maximum body size (C. cornuta: 539–554 μm; M. macrocopa: 1274.8–1309 μm) reached by either of the cladocerans. The maximum body sizes were larger than size at first reproduction with either of the ciliated protists, however, with algal diet the maximum body sizes did not differ from the size at first reproduction in each case. In case of C. cornuta the generation time (20.5 ± 0.3 days on ciliate; 15.6 ± 0.17 days on algal diet), reproductive rates (net reproductive rate: 20.05 ± 3.2 on ciliate; 15.5 ± 1.2 on algal diet), and average life expectancy at hatching (27 ± 0.8 days on ciliate; 22.7 ± 0.71 days on alga) were higher, whereas the size at first reproduction (482 μm on ciliate; 521 μm on alga) was smaller with the ciliate than with an algal diet. The algal and the ciliate diets did not differ in survival (life expectancy at hatching: 9.2 ± 0.7 days) and fecundity (NRR: 23.6 ± 2.4) for M. macrocopa. The two ciliates used in the experiment did not differ in their performance as food source for either cladoceran species. Our results suggest that both the cladoceran species are able to utilize smaller ciliate (e.g., T. pyriformis, C. (c.f.) steini) as food; however with differential ability to derive energy from the ciliate diet and this ability is size and age structured in both cases. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

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.     

Lack of compensatory body growth in a high performance moose Alces alces population

Considerable work has been done on disentangling important factors determining early development in body size, yet our knowledge of the extent to which animals living under varying conditions can achieve catch-up growth for a bad start in life is limited. Here, we investigated how body mass at the age of 8 months influenced adult body mass in a moose Alces alces population living under excellent environmental conditions on the island of Vega in northern Norway. We also investigated if mother age and birth date effects on calf body mass persisted until adulthood. We show that neither males nor females were able to show compensatory growth before they reached adulthood, and that part of the variation in adult body mass may have been due to variation in mother age and date of birth. The pattern observed in males can be related to their growth strategy in relation to reproduction, while such results were not expected in females where size-dependent start of reproduction is likely to interact with body growth. We suggest that the good environmental conditions experienced on Vega led to females having small somatic costs of an early start of reproduction or that larger females were able to acquire more resources for growth than their smaller conspecifics. In both cases, females that postpone their first reproduction may not be able to achieve catch-up growth for their lower early body mass compared to females that start reproduction at an early age. Our results concur with previous studies indicating that compensatory growth is weak in moose, increasing the likelihood that variation in life history characters are also transferred between generations.     

Small body size in an insect shifts development, prior to adult eclosion, towards early reproduction

Life-history theory has suggested that individual body size can strongly affect the allocation of resources to reproduction and away from other traits such as survival. In many insects, adults eclose with a proportion of their potential lifetime egg production that is already mature (the ovigeny index). We establish for the solitary parasitoid wasp Aphaereta genevensis that the ovigeny index decreases with adult body size, despite both initial egg load and potential lifetime fecundity increasing with body size. This outcome is predicted by adaptive models and is the first unequivocal intraspecific demonstration. Evidence suggests that a high ovigeny index carries a cost of reduced longevity in insects. Our results therefore contribute to the emerging evidence that small body size can favour a developmental shift in juveniles that favours early reproduction, but which has adverse late-life consequences. These findings are likely to have important implications for developmental biologists and population biologists.     

Altitudinal variation in age and body size in Yunnan pond frog (Pelophylax pleuraden)

Large-scale systematic patterns of body size are a basic concern of evolutionary biology. Identifying body size variation along altitudinal gradients may help us to understand the evolution of life history of animals. In this study, we investigated altitudinal variation in body size, age and growth rate in Chinese endemic frog, Pelophylax pleuraden. Data sampled from five populations covering an altitudinal span of 1413 to 1935 m in Sichuan province revealed that body size from five populations did not co-vary with altitudes, not following Bergmann's rule. Average adult SVL differed significantly among populations in males, but not in females. For both sexes, average adult age differed significantly among populations. Post-metamorphic growth rate did not co-vary with altitude, and females grew faster than males in all populations. When controlling the effect of age, body size did not differ among populations in both sexes, suggesting that age did not affect variation in body size among populations. For females, there may be other factors, such as the allocation of energy between growth and reproduction, that eliminated the effect of age on body size. To our minds, the major reason of body size variation among populations in male frogs may be related to individual longevity. Our findings also suggest that factors other than age and growth rate may contribute to size differences among populations.     

Sociality, age at first reproduction and senescence: comparative analyses of birds

Evolutionary theories of senescence suggest that aging evolves as a consequence of early reproduction imposing later viability costs, or as a consequence of weak selection against mutations that act late in life. In addition, highly social species that live in sites that are protected from extrinsic mortality due to predation should senesce at a slower rate than solitary species. Therefore, species that start reproducing late in life should senesce at a slower rate than species that start reproducing early. In addition, social species should senesce more slowly than solitary species. Here I investigate the rate of senescence using an extensive data set on longevity records under natural field conditions to test predictions about the evolution of senescence among 271 species of birds. Longevity records increased with sampling effort and body mass, but once these confounding variables were controlled statistically, there was a strongly positive relationship between relative longevity and relative adult survival rate. Relative longevity after controlling statistically for sampling effort, body mass and adult survival rate, increased with age at first reproduction, but not with degree of breeding sociality. These findings suggest that the evolution of senescence is related to timing of first reproduction, but that the evolution of breeding sociality has played a negligible role in the evolution of senescence.     

A comparison of the reproductive strategies of three species of Dysdercus from Africa (Hemiptera,Pyrrhocoridae)

Summary Reproductive strategies have been investigated for three species of Dysdercus from Africa, D. intermedius, D. cardinalis and D. nigrofasciatus. Reproductive parameters were measured for each species on individuals cultured in the laboratory. D. cardinalis is associated more with herbaceous than with arboreal host plants and is intermediate in body size. It tended to have the least age at first reproduction, reproduced most frequently, and layed the smallest clutches on average, spreading relatively high amounts of parental investment in more clutches than the other two species. It also laid the greatest number of clutches and eggs in a lifetime. D. intermedius specializes on arboreal host plants, and is the largest of the three species. It had the greatest age at first reproduction, reproduced less frequently than D. cardinalis, and layed the largest clutches. Its parental investment over time declined earlier than that of D. cardinalis. D. intermedius layed the least number of clutches in a lifetime, but its lifetime gross reproduction was intermediate in magnitude. D. nigrofasciatus has the widest diet breadth, and is the smallest in body size. Its age at first reproduction was similar to that of D. cardinalis, but D. nigrofasciatus reproduced least frequently, laying relatively large clutches. It was similar to D. intermedius in its pattern of parental investment over time, and essentially layed the same number of clutches in a lifetime as the latter species, although its lifetime gross reproduction was the smallest.It is suggested that the reproductive strategies of the three species might have evolved as adaptations to selection events in the niches of the immature stages.     

THE EFFECTS OF BODY MASS,PHYLOGENY, HABITAT,AND TROPHIC LEVEL ON MAMMALIAN AGE AT FIRST REPRODUCTION

I examined age at first reproduction of 547 mammalian species to determine the influence of diet and habitat on the evolution of life-history traits. Body mass correlated positively with age at first reproduction, explaining 56% of the variance. Habitat and trophic groups deviated significantly from the allometric curve in a pattern generally consistent with predictions from r/K selection theory and its modifications. However, mammalian orders also deviated significantly from the allometric curve, and different habitat and diet groups contained different ratios of mammalian orders. When the effects of orders were removed, residual deviations did not differ among ecological groups. Adjusting for ecological differences did not eliminate the differences between orders. These results suggest that body mass (or some correlated factor) and phylogeny strongly constrain age at first reproduction. Ecological factors appear to have little effect on the evolution of age at first reproduction. Apparent differences in weight-specific ages at first reproduction within habitats and trophic groups may be the result of ecological selection of order composition in the present, rather than ecologically driven evolution of life history in the past.     

Is sociality associated with high longevity in North American birds?

Sociality, as a life-history trait, should be associated with high longevity because complex sociality is characterized by reproductive suppression, delayed breeding, increased care and survival, and some of these traits select for high longevity. We studied the relationship between cooperative parental care (a proxy of complex sociality) and relative maximum lifespan in 257 North American bird species. After controlling for variation in maximum lifespan explained by body mass, sampling effort, latitude, mortality rate, migration distance and age at first reproduction, we found no significant effect of cooperative care on longevity in analyses of species-specific data or phylogenetically independent standardized linear contrasts. Thus, sociality itself is not associated with high longevity. Rather, longevity is correlated with increased body size, survival rate and age of first reproduction.     

Is bigger better? The relationship between size and reproduction in female Asian elephants

The limited availability of resources is predicted to impose trade‐offs between growth, reproduction and self‐maintenance in animals. However, although some studies have shown that early reproduction suppresses growth, reproduction positively correlates with size in others. We use detailed records from a large population of semi‐captive elephants in Myanmar to assess the relationships between size (height and weight), reproduction and survival in female Asian elephants, a species characterized by slow, costly life history. Although female height gain during the growth period overlapped little with reproductive onset in the population, there was large variation in age at first reproduction and only 81% of final weight had been reached by peak age of reproduction at the population level (19 years). Those females beginning reproduction early tended to be taller and lighter later in life, although these trends were not significant. We found that taller females were more likely to have reproduced by a given age, but such effects diminished with age, suggesting there may be a size threshold to reproduction which is especially important in young females. Because size was not linked with female survival during reproductive ages, the diminishing effect of height on reproduction with age is unlikely to be due to biased survival of larger females. We conclude that although reproduction may not always impose significant costs on growth, height may be a limiting factor to reproduction in young female Asian elephants, which could have important implications considering their birth rates are low and peak reproduction is young – 19 years in this population.     

Interval between clutches, fitness, and climate change

Timing of optimal reproduction can be affected by the presenceof multiple broods, with multi-brooded species breeding earlier(and later) than the optimal timing of breeding as comparedwith single-brooded species that only need to optimize the timingof a single brood. Approximately two-thirds of barn swallowsHirundo rustica produce 2 broods per year, and I tested whetherthe constraints on timing of reproduction were affected by climatechange because climatic amelioration would allow both an earlierstart and a later termination of reproduction. The durationof the interval between first and second clutches and the variancein the duration increased during 1971–2005 when temperatureduring spring, but not summer, increased rapidly. Interclutchinterval was shorter when mean date of breeding was late andalso among late-breeding individuals during individual years.When clutch size and brood size of the first clutch were large,interval until the second brood increased. Pairs with a longinterval produced more fledglings than pairs with a short interval.Pairs with first broods with strong mean T-cell–mediatedimmune responses took shorter time to start their second clutch,whereas mean body mass or tarsus length of first broods werenot significantly related to interclutch interval. Interclutchinterval increased with the size of a secondary sexual character,the length of the outermost tail feathers of adult male barnswallows, but not with tail length of females, or with sizeof several other phenotypic characters in either sex. Thesefindings are consistent with the hypothesis that the durationof the interclutch interval is determined by a combination ofenvironmental conditions, reproductive effort, and sexual selection.     

Maturity, mating and age-specific reproductive effort of the snake Natrix maura

The ecology of reproduction was studied in the snake Natrix maura. The presence of sperm in cloacal fluid was used to show the size at maturity, the season of mating and, together with information on the persistence of sperm in cloacal fluid of females after mating, the frequency of mating. These results suggest that each female mated several times per year. Female N. maura grew substantially after maturity, and clutch size increased with body size. Current and expected future reproduction increased in parallel during the period of growth after maturity; subsequently they were constant. This pattern would be expected to lead to a constant proportional allocation of energy to current reproduction. Reproductive effort (eggs/body energy) was independent of age as measured by growth rings. There was some evidence that not all stored energy was used in reproduction in the current season even when some follicles regressed.     

Determinants of reproductive success in female adders,Vipera berus

Summary Female lifetime reproductive success in a small population of individually-marked adders in southern Sweden was studied over a period of seven years. Reproductive characteristics varied little from year to year and were consistent through time in individual females. Most females mature at four years of age and reproduce every two years. The total number of offspring produced by a female depends on her adult body size (and thus, litter size) and longevity (and thus, number of litters per lifetime). Adult body size in females is influenced mainly by subadult growth rates. Offspring size depends on maternal body size and a tradeoff between offspring size and offspring number. Maternal age does not affect litter sizes and offspring sizes except through ontogenetic changes in maternal body size.Survival of females after parturition is low because of the high energy costs of reproduction, compounded by low feeding rates of gravid females because of their sedentary behaviour at this time. About one-half of females produce only a single litter during their lifetimes, although some females live to produce four or five litters. On a proximate basis, rates of energy accumulation for growth (in subadults) and reproduction (in adults) may be the most important determinants of fitness in female adders.     

Seasonality determines patterns of growth and age structure over a geographic gradient in an ectothermic vertebrate

Environmental variation connected with seasonality is likely to affect the evolution of life-history strategies in ectotherms, but there is no consensus as to how important life-history traits like body size are influenced by environmental variation along seasonal gradients. We compared adult body size, skeletal growth, mean age, age at first reproduction and longevity among 11 common frog (Rana temporaria) populations sampled along a 1,600-km-long latitudinal gradient across Scandinavia. Mean age, age at first reproduction and longevity increased linearly with decreasing growth season length. Lifetime activity (i.e. the estimated number of active days during life-time) was highest at mid-latitudes and females had on average more active days throughout their lives than males. Variation in body size was due to differences in lifetime activity among populations??individuals (especially females) were largest where they had the longest cumulative activity period??as well as to differences between populations in skeletal growth rate as determined by skeletochronological analyses. Especially, males grew faster at intermediate latitudes. While life-history trait variation was strongly associated with latitude, the direction and shape of these relationships were sex- and trait-specific. These context-dependent relationships may be the result of life-history trade-offs enforced by differences in future reproductive opportunities and time constraints among the populations. Thus, seasonality appears to be an important environmental factor shaping life-history trait variation in common frogs.