Life‐history traits of the long‐nosed skate Dipturus oxyrinchus

This work investigates life‐history traits of the long‐nosed skate Dipturus oxyrinchus, which is a common by‐catch in Sardinian waters. The reproductive variables were analysed from 979 specimens sampled during scientific and commercial hauls. Females (10·4–117·5 cm total length, L_T) attained larger sizes than males (14·5–99·5 cm L_T). To evaluate age and growth, a sub‐sample of 130 individuals (76 females and 54 males) were used. The age was estimated by annuli counts of sectioned vertebral centra. Four models were used for the length‐at‐age data: the von Bertalanffy, the exponential, the Gompertz and the logistic functions. According to the Akaike's information criterion, the Gompertz model seemed to provide the best fitting curve (L_∞ mean ± s.e. : 127·55 ± 4·90 cm, k: 0·14 ± 0·09, IP: 3·97 ± 0·90 years). The oldest female and male were aged 17 (115·5 cm L_T) and 15 years (96·0 cm L_T), respectively. Lengths at maturity were 103·5 cm for females and 91·0 cm for males, corresponding to 90% of the maximum observed length in both sexes. The monthly distribution of maturity stages highlighted an extended reproductive cycle, with spawning females and active males being present almost throughout the year, as confirmed by the gonado‐somatic index. Ovarian fecundity reached a maximum of 26 yolked follicles with a mean ± s.e. size of 19·7 ± 6·5 mm.     

Life‐history traits and population decline of the Atlantic mackerel Scomber scombrusin the Adriatic Sea

This study investigated demographic structure and reproductive characteristics of the Atlantic mackerel Scomber scombrus, in relation to landing trends in the northern‐central Adriatic Sea. Results highlighted the occurrence of only small‐sized and young‐age individuals, and a marked decline from the 1990s to the present in maximum age (from 8 to 3 years) and total length (L_T; from 420 to 360 mm). Fecundity ranged between 40 000 and 190 000 eggs, and was related to female L_T. High levels of atresia implied lower values of actual fecundity. Sexual maturity was attained by 72·8% of individuals in their first year of life at 200 mm. The reduction in maximum L_T resulted in a marked decline in the population egg production, while the reduction in maximum age implied that females participated in fewer spawning events.     

Life‐history traits of the stone loach Barbatula barbatula

The life‐history tactics of the stone loach Barbatula barbatula were studied in a Mediterranean‐type climate stream (Matarranya River) located in the Ebro River basin (north‐east Spain). Maximum observed ages were 2+ years in both sexes (1% of individuals), although only 0+ and 1+ year age groups were well represented. It is the lowest longevity reported for this species in its entire distribution. The seasonal growth period started in June and continued until November, but the pattern observed was different to northern populations. Barbatula barbatula in the Matarranya River was a multiple spawner, releasing small batches of oocytes between April and June. The fecundity of females was higher and the size of oocytes smaller in 1984 than in 1985. The relative fecundity (number of ripening and ripe oocytes g^?1 of fish) was lower than in northern European populations. The role of the particular environmental conditions of a Mediterranean stream was discussed in relation to the life‐history tactics of B. barbatula.     

Life‐history characteristics of the large Amazonian migratory catfish Brachyplatystoma rousseauxii in the Iquitos region,Peru

The main life‐history traits of the dorado Brachyplatystoma rousseauxii, a large Amazonian catfish undertaking the largest migration known for a freshwater fish species (from the nursery area in the estuary of the Amazon to the breeding zones in the head waters of the western Amazon basin close to the Andes), were determined from a 5 year sampling of >15 000 specimens in the Peruvian Amazon. The breeding season occurred during the falling and low‐water periods, which is hypothesized to be an adaptation to maximize the chances of young stages to reach the estuary. The size at first sexual maturity was slightly larger for females than males, c. 91 and 83 cm standard length (L_S), respectively. Both males and females reproduce for the first time at >3 years old. The fecundity per spawning event ranged from 481 734 to 1 045 284 oocytes for females weighing 25 and 34 kg, respectively. Seasonal variations of body condition were similar among sexes, but differed between immature specimens that had a higher condition during the low‐water period and lower condition during rising waters, and mature individuals that showed the opposite pattern. The growth characteristics were estimated by L_S frequency analysis. For females, the best fitting models gave a mean birth date in August, during the height of the breeding cycle, with the following von Bertalanffy growth function parameters: L_S∞ = 153·3, K = 0·29 and t₀ =– 0·37 years. For males, the best fitting model gave a mean birth date in July, also during the height of the breeding period, with L_S∞ = 142, K = 0·30 and t₀ =– 0·36 years. At a given age, females were systematically larger than males and the size difference increased with age. The largest females sampled (148 cm L_S) was 11 years old and the largest male (134 cm L_S) was 9 years old. The mortality estimates were higher for males total (Z) = 1·34, natural (M) = 0·52 and fishing (F) = 0·82 than for females (Z = 0·98, M = 0·50, F = 0·48). The life‐history patterns of B. rousseauxii are discussed in light of the available knowledge about this species and the understanding of its complex life cycle.     

Life‐history strategies of the rock hind grouper Epinephelus adscensionis at Ascension Island

Epinephelus adscensionis sampled from Ascension Island, South Atlantic Ocean, exhibits distinct life‐history traits, including larger maximum size and size at sexual maturity than previous studies have demonstrated for this species in other locations. Otolith analysis yielded a maximum estimated age of 25 years, with calculated von Bertalanffy growth parameters of: L_∞ = 55·14, K = 0·19, t₀ = ?0·88. Monthly gonad staging and analysis of gonad‐somatic index (I_G) provide evidence for spawning from July to November with an I_G peak in August (austral winter), during which time somatic growth is also suppressed. Observed patterns of sexual development were supportive of protogyny, although further work is needed to confirm this. Mean size at sexual maturity for females was 28·9 cm total length (L_T; 95% C.I. 27·1–30·7 cm) and no females were found >12 years and 48·0 cm L_T, whereas all confirmed males sampled were mature, >35·1 cm L_T with an age range from 3 to 18 years. The modelled size at which 50% of individuals were male was 41·8 cm (95% C.I. 40·4–43·2 cm). As far as is known, this study represents the first comprehensive investigation into the growth and reproduction of E. adscensionis at its type locality of Ascension Island and suggests that the population may be affected less by fisheries than elsewhere in its range. Nevertheless, improved regulation of the recreational fishery and sustained monitoring of abundance, length frequencies and life‐history parameters are needed to inform long‐term management measures, which could include the creation of marine reserves, size or temporal catch limits and stricter export controls.     

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.     

Life‐history traits of gaur Bos gaurus: a first analysis

In this first detailed analysis of gaur Bos gaurus life‐history traits, data were collected from a 20‐month field study in South India and from captive gaur populations. Mean age of females at first parturition was 3 years; females remained fertile beyond the age of 15 years. Adult females were three times more abundant than adult males in the wild; survival of females was greater than males beyond three years of age. Life span of both sexes has not exceeded 24 years in captivity. Gaur life‐history traits are similar to those of other similar‐sized Bovini species.     

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.     

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.     

Life‐history traits of the Northwest European flora: The LEDA database

Abstract. An international group of scientists is building a ‘trait base’, an open internet database of life‐history traits of the Northwest European flora (LEDA) that can be used as a tool in planning, in nature conservation and restoration, and in other applied research. The species‐trait matrix will comprise referenced information under control of an editorial board, for species of the Northwest European flora, combining existing information and additional measurements. The focus will be on 26 plant traits that describe three key features of plant dynamics: persistence, regeneration, and dispersability. Currently 35% of the species‐trait matrix has been filled; however, as the LEDA trait base consortium aims to deliver a database as complete as possible, all input from the scientific community is welcome.     

Geographical variation in reproductive ageing patterns and life‐history strategy of a short‐lived passerine bird

We investigated differences in ageing patterns in three measures of breeding performance in populations of barn swallows Hirundo rustica L. from Spain and Denmark differing in breeding latitude and hence migration distance and duration of the breeding season. We found differences in ageing patterns between populations. Generally, young (i.e. yearling) and old females (i.e. ≥ 5 years of age) laid their first eggs later and produced smaller clutches than middle‐aged females (i.e. 2–4 years of age) in both populations. The southernmost population (i.e. Spanish) showing the shorter migratory distance experienced a greater within‐individual increase in timing of breeding and clutch size in early life and a greater within‐individual decrease in laying date but not in clutch size during senescence compared with the northernmost population (i.e. Danish). We also found that the number of fledglings produced annually was related to the age of the two members of the breeding pairs with pairs composed of young and old females performing less well than breeding pairs composed of middle‐aged females. We did not find reproductive senescence for the age of the male while controlling for the age of the female on the number of fledglings produced annually by the breeding pair. Differential survival between individuals did not explain age effects on laying date or annual clutch size in neither population. However, the increase in the number of fledglings produced annually with age was partly explained by the disappearance of poor‐quality members of the pairs, mainly poor‐quality males. Age‐related breeding success (i.e. number of fledglings) was similar for barn swallows from Spain and Denmark. Therefore, the study of ageing patterns and life‐history strategies in free‐ranging animals from more than a single population can throw new light on life‐history theory, population dynamics and evolutionary studies of senescence.     

On the life history of the lesser gurnard (Scorpaeniformes: Triglidae) inhabiting the Agulhas Bank, South Africa

Growth analysis based on sectioned sagittal otoliths revealed the lesser gurnard Chelidonichthys queketti on the Agulhas Bank to be relatively fast growing and long lived, with ages of up to 7 years being recorded. Total length at age (mm) was described best by the specialized von Bertalanffy growth model as L _T=306·1 (1 − e^{0·53(t+0·18)}). First approximations of total, natural and fishing mortality rates were determined at 0·73, 0·38 and 0·35 year⁻¹ respectively. The adult population was male dominated with a sex ratio of 1 female: 1·2 males with the mean size of males and females being similar. The lesser gurnard is an iteroparous species with females maturing by the end of the first year of life (195 mm L _T), thereafter spawning throughout the year with reproductive activity peaking over spring and late summer. The lesser gurnard appears to exhibit similar life-history patterns to other triglid species in that it can be classified as a generalist. Generalistic life-history characteristics such as a fast growth rate, early sexual maturity at a relatively large size, a non-seasonal spawning pattern, feeding on a variety of prey organisms and the ability to inhabit various substrata could all contribute to it maintaining a high biomass on the Agulhas Bank.     

Determinants and long‐term costs of early reproduction in males of a long‐lived polygynous mammal

In long‐lived polygynous species, male reproductive success is often monopolized by a few mature dominant individuals. Young males are generally too small to be dominant and may employ alternative tactics; however, little is known about the determinants of reproductive success for young males. Understanding the causes and consequences of variability in early reproductive success may be crucial to assess the strength of sexual selection and possible long‐term trade‐offs among life‐history traits. Selective pressures driven by fluctuating environmental conditions may depend on age class. We evaluated the determinants of reproduction in male bighorn sheep (Ovis canadensis) aged 2–4 years using 30 years of individual‐level data. These young males cannot defend estrous ewes and use alternative mating tactics. We also investigated how the age of first detected reproduction was correlated to lifetime reproductive success and longevity. We found that reproductive success of males aged 3 years was positively correlated to body mass, to the proportion of males aged 2–4 years in the competitor pool, and to the number of females available per adult male. These results suggest that reproductive success depends on both competitive ability and population age–sex structure. None of these variables, however, had significant effects on the reproductive success of males aged 2 or 4 years. Known reproduction before the age of five increased lifetime reproductive success but decreased longevity, suggesting a long‐term survival cost of early reproduction. Our analyses reveal that both individual‐level phenotypic and population‐level demographic variables influence reproductive success by young males and provide a rare assessment of fitness trade‐offs in wild polygynous males.     

Assortative mating patterns of multiple phenotypic traits in a long‐lived seabird

Choosing the right mate is crucial for successful breeding, particularly in monogamous species with long and extensive bi‐parental care, and when the breeding pair is presumed to last many seasons. We investigated the degree of assortative mating in the Little Auk Alle alle, a long‐lived seabird with long‐term pair bonds and bi‐parental care for fixed (morphological) and labile (physiological, behavioural) traits. Using randomization tests, we suggest assortative mating with respect to wing length, extent of the white area on the upper eyelid and hormonal stress response (the difference between stress‐induced and baseline corticosterone levels). We discuss how the assortative mating patterns that we found in the Little Auk may be adaptive.     

Predator-induced plasticity in guppy (<Emphasis Type="Italic">Poecilia reticulata</Emphasis>) life history traits

A number of invertebrates show predator-induced plasticity in life-history and morphological traits that are considered adaptive. Evidence is accumulating that vertebrates may also adjust their life-history traits in response to predators; however, some of the patterns of plasticity, which appear to be an adaptive response specifically to the risk of size-selective predation, may instead result from reduced foraging in response to predator presence. Here, we describe a study of predator-induced plasticity in guppies (Poecilia reticulata). We have predicted that the plastic response to cues from a small, gape-limited, natural predator of guppies, the killlifish (Rivulus hartii), would be the opposite of that caused by reduced food intake. We have found that male guppies increased their size at maturity, both length and mass, in response to the non-lethal presence of this predator. This pattern of plasticity is the opposite of that observed in response to reduced food intake, where male guppies reduce size at maturity. The increase in size at maturity that we observed would likely reduce predation on adult male guppies by this native predator because it is gape-limited and can only eat juvenile and small adult guppies. This size advantage would be important especially because male guppies grow very little after maturity. Therefore, the pattern of plasticity that we observed is likely adaptive. In contrast, female guppies showed no significant response in size at first parturition to the experimental manipulation; however, we did find evidence suggesting that females may produce more, smaller offspring in response to cues from this predator.     

Life‐history traits of the common snook Centropomus undecimalis in a Caribbean estuary and large‐scale biogeographic patterns relevant to management

The ecology of common snook Centropomus undecimalis in Amatique Bay, a tropical estuary in eastern Guatemala, was investigated and life‐history traits were used to conduct a meta‐analysis of the species from Florida to Brazil. The reproduction cycle of C. undecimalis in Amatique was strongly related to the precipitation cycle, with a lag of 2 months. Spawning occurred from April to November with a peak spawning after the onset of the summer rains. Protandric sex reversal occurred early in the dry season (December) before somatic recovery from spawning. The growth cycle preceded that of body condition by c. 1 month, and was out of phase with the reproductive cycle. Growth was fast, as many individuals reached >70% of the maximum observed total length (L_T, 102 cm) after 3 years. Sex transition occurred within a relatively narrow L_T range (70–79 cm), but over a wide range of ages, indicating plasticity in this respect. The meta‐analysis indicated a latitudinal‐temperature gradient in life‐history traits, as well as different seasonal patterns relative to temperature and hydrographical cycles. Centropomus undecimalis from cooler winter waters (e.g. Florida) reach larger maximum L_T and L_T at sex change, as well as greater gonado‐somatic indices and longer life spans. Further, increased fishing mortality results in younger age at sex reversal and male predominance in the populations compared. Recognition of large‐scale biogeographic patterns in this important, but little studied, fish species helps in the formulation of management advice in other areas of its occurrence.     

Cryptic inbreeding depression in a growing population of a long‐lived species

Genetic effects are often overlooked in endangered species monitoring, and populations showing positive growth are often assumed to be secure. However, the continued reproductive success of a few individuals may mask issues such as inbreeding depression, especially in long‐lived species. Here, we test for inbreeding depression in little spotted kiwi (Apteryx owenii) by comparing a population founded with two birds to one founded with 40 birds, both from the same source population and both showing positive population growth. We used a combination of microsatellite genotypes, nest observations and modelling to examine the consequences of assessing population viability exclusively via population growth. We demonstrate (i) significantly lower hatching success despite significantly higher reproductive effort in the population with two founders; (ii) positive growth in the population with two founders is mainly driven by ongoing chick production of the founding pair; and (iii) a substantial genetic load in the population founded with two birds (10–15 diploid lethal equivalents). Our results illustrate that substantial, cryptic inbreeding depression may still be present when a population is growing, especially in long‐lived species with overlapping generations.