Dimensionless numbers and life history variation in Brown Trout

Summary Dimensionless numbers, made up from components of life history as defined by growth, mortality and maturation, may provide fresh insights into life history evolution. Most studies have previously shown that these numbers are more or less constants within taxa. The variation between taxa may clarify the evolution of different life histories. We examine the variation in three dimensionless numbers using data from 29 populations of Brown TroutSalmo trutta from Norway, and find that the dimensionless numbers are not constants for the Brown Trout populations. We find that the relationship betweenK of the von Bertalanffy growth equation and the mortality rate (M) increased with increasing growth rate. Also, relative length at maturity (L /L _inf) increased with increasing asymptotic length (L _inf). We suggest that more such data should be collected from a large number of species and taxonomic groups, to allow a more detailed assessment of why these dimensionless numbers appear to be constants in some taxa and not in others.     

Age-specific mortality rates in reef fishes: Evidence and implications

Abstract Mortality is a fundamental demographic rate, the nature of which has profound consequences for both the dynamics of populations and the life-history evolution of species. For example, if per capita mortality rates are age- or stage-specific, life-history traits should evolve in response to age- and stage-specific differences in selection arising from these temporally variable rates. Similarly, variation in the average mortality rate across ages and/or stages can also select for shifts in life history. Mortality rates of recently settled reef fishes can be very high and per capita mortality is commonly assumed to decrease with increasing age. A review of evidence for age-specific per capita mortality rates in reef fishes from early postsettlement up to 13 months postsettlement suggests that during this period these rates are often age invariant. The data on which these interpretations are based, however, are extremely limited both in terms of the proportion of the life cycle over which mortality rates have been sampled and the quality of these data. Nonetheless, these data do suggest that selective pressures associated with patterns of mortality may vary among species of reef fishes and that these species therefore could be more effectively used in the study of life-history evolution. At present, reef fishes are under-represented in the study of life-history evolution compared with other vertebrate taxa.     

The evolution of fledging age in songbirds

In birds with altricial young an important stage in the life history is the age at fledging. In this paper we use an approach proven successful in the prediction of the optimal age at maturity in fish and reptiles to predict the optimal age of fledging in passerines. Integrating the effects of growth on future fecundity and survival leads to the prediction that the optimal age at fledging is given by a function that comprises survival to maturity, the exponent of the fecundity-body size relationship and nestling growth. Growth is described by the logistic equation with parameters, A, K and t(i). Assuming that the transitional mortality curve can be approximated by the nestling mortality, M(n), the optimal fledging age, t(f), is given by a simple formula involving the three growth parameters, nestling mortality (M(n)) and the exponent (d) of the fecundity-body size relationship. Predictions of this equation underestimate the true values by 11-16%, which is expected as a consequence of the transitional mortality function approximation. A transitional mortality function in which mortality is approximately 0.3-0.4 of nesting mortality (i.e. mortality declines rapidly after fledging) produces predictions which, on average, equal the observed values. Data are presented showing that mortality does indeed decline rapidly upon fledging.     

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.     

Evolution of resource allocation between growth and reproduction in animals with indeterminate growth

We review the recent theoretical developments explaining the evolution of age-schedules of reproduction in animals with indeterminate growth. Indeterminate growth, i.e. growth that continues past maturation and may continue until the end of life, is characteristic for a large number of invertebrate taxa (e.g. clams, cladocerans and crayfish) and ‘lower’ vertebrate taxa (e.g. fish, amphibians, lizards and snakes). Many plants also exhibit indeterminate growth, and we liberally include studies focused on plants when they can be interpreted in terms of animal life histories. We focus on different measures used to determine the fittest life histories, on indeterminate growth as a problem of resource allocation and on the effects of environment to the evolution of the resource allocation schemes.     

Life history of the cownose ray, <Emphasis Type="Italic">Rhinoptera bonasus</Emphasis>, in the northern Gulf of Mexico,with comments on geographic variability in life history traits

Synopsis We determined age and growth, size at maturity, and fecundity for cownose rays, Rhinoptera bonasus, collected from the northern Gulf of Mexico. Vertebral age estimates ranged from 0+ to 18+ years for females and 0+ to 16+ years for males. Annual deposition of growth increments was verified with marginal increment analysis. Likelihood ratio tests indicated that the growth of the cownose ray was best described by a combined sexes Gompertz model. Median size at 50% maturity was determined to be 642 mm DW for males and 653 mm DW for females, or 4–5 years of age. Median pup size-at-birth was estimated to be 350 mm DW, with a gestation period of 11–12 months. In all cases, gravid females contained only one pup. Statistically significant differences were detected between growth curves for the Gulf of Mexico and the western Atlantic Ocean. Cownose rays in the Gulf of Mexico had lower estimates of DW_∞ and K, and a higher theoretical longevity than their conspecifics in the western Atlantic Ocean. Cownose rays in the Gulf of Mexico also attain maturity at a smaller size and earlier age than their counterparts in the western Atlantic Ocean.     

Growth of the clupeid fishes, Stolothrissa tanganicae and Limnothrissa miodon, in the Zambian waters of Lake Tanganyika

The age and growth of two endemic Lake Tanganyikan clupeid fishes, Stolothrissa tanganicae and Limnothrissa miodon , were estimated from analysis of otolith microstructure in specimens collected in Zambian waters from October to December 1990. Both species had relatively clear, concentric otolith increments which were believed to represent daily increments based on their similarity to daily increments found in some marine clupeid species. The growth rates estimated from length-at-age data were: for S. tanganicae, L_t = 104·0 (1 – exp (– 0.00512 ( t – 5·8))); for L. miodon, L_t = 155.4 (1 – exp (– 0.00236 ( t +8.1))). In most cases, the growth parameters obtained from otolith analyses generally agreed with those previously estimated from analyses of length-frequency distributions.     

西藏浪错兰格湖裸鲤的年龄与生长

2017年7月—2018年5月,于西藏自治区昂仁县浪错采集268尾兰格湖裸鲤Gymnocypris chui开展种群年龄结构和生长特征研究。结果显示:雌、雄鱼体长与体质量的关系式分别为W♀=2.03×10-2L2.822(n=134,R2=0.969)、W♂=2.52×10-2L2.738(n=105,R2=0.966)。通过观察微耳石,发现样本由1~23龄组成;采用VonBertalanffy生长方程拟合雌、雄鱼体长、体质量生长方程:Lt♀=34.239[1-e-0.136(t+0.11)]、Wt♀=434.42[1-e-0.136(t+0.11)]2.822;Lt♂=32.201[1-e-0.136(t+0.287)]、Wt♂=338.8[1-e-0.136(t+0.287)]2.738;拐点年龄分别为7.52龄和7.12龄,对应体长分别为22.12cm和20.45cm,体质量分别为126.59g和97.71g。初步研究表明,兰格湖裸鲤生长慢、体型小,种群被破坏后不易恢复,亟待开展资源评估及保护工作。