Temporal and latitudinal comparisons of reproductive parameters in a heavily exploited shark,the bonnethead,Sphyrna tiburo (L. 1758), in the southern Gulf of Mexico

In the southern Gulf of Mexico, the bonnethead shark, Sphyrna tiburo, is one of the most frequently captured species in landings of small-scale fisheries. Based on the analysis of two fishery-dependent sampling periods (1993–1994 and 2007–2014), this study aimed to determine reproductive parameters and identify temporal differences between the two time periods. In the first sampling period, 776 males and 352 females with a size range of 28.0–120.0 cm total stretched length (L_T) were analysed, and in the second sampling period, 387 males and 432 females with a size range of 28.0–122.0 cm L_T were analysed. The size at 50% maturity in the second sampling period was significantly different between sexes, 82.6 cm L_T for females and 73.8 cm L_T for males (no estimation was possible for the first sampling period). The size at 50% maternity was not different between sampling periods, 97.3 cm L_T for the first sampling period and 99.0 cm L_T for the second sampling period. Litter size varied from 3 to 19 embryos and the average was not statistically different in both periods, 10.1 (S.D. = 3.8) for the first sampling period and 11.3 (S.D. = 3.5) for the second sampling period. The female reproductive cycle is asynchronous, and it seems to be annual, with a gestation period of 5–6 months, and a consecutive ovarian cycle and gestation period. Temporal (between sampling periods) and latitudinal (southern Gulf versus northern regions) variations occur in the synchronicity of the reproductive cycle, temporal variation in the relationship between maternal length and litter size, and latitudinal variation in average size of mature sharks.     

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.     

Life History Variation in Female Gambusia hubbsi

Gambusia hubbsi populations occur in a variety of fresh and brackish-water habitats on Andros, Bahamas. These include shallow water sites (tidal creeks, lakes, roadside ditches), and blueholes (vertical solution caves). In some blueholes G. hubbsi is the only species present, in others it co-occurs with other species, principal among these is a predator, Eleotris pisonis. By contrast to blueholes, shallow water sites have highly variable temperature and depth. In addition, they are frequented by avian piscivores and may be occasionally occupied by piscivores such as Eleotris. We sampled 10 shallow water sites, 14 blueholes where Eleotris is absent and 12 blueholes where Eleotris co-occurs with G. hubbsi. We measured and compared variation in female body size, fecundity, and reproductive investment among these three habitats. The observed patterns of life history variation are only partially in accord with expectations from theory regarding the effects of predation and seasonality on life history variation. Samples from populations that colonized a series of man-made trenches (Well Fields), a set of introductions into that habitat, and changes in life history traits of lab-raised females from three blueholes, suggest that the observed pattern of life history variation in other habitats also reflects differences in food availability among habitats, and imperfectly reflects the potential phenotypic variability of this species.     

The quantitative genetics of growth in a field cricket

Because of its relationship with both development time and adult size, the rate of growth in determinately growing organisms is an important aspect of their life histories. We reared sixty-nine families of Gryllus pennsylvanicus derived from a natural population and found significant genetic variation in growth rate as estimated by the slope of linearized growth trajectories. We found no evidence for a genetic tradeoff between rate of growth and survival, nor rate of growth and fecundity. In principle, adult size may be determined both by the rate of growth and the time taken by the nymphs to develop. Our data indicate that variation in adult size is explained by variation in growth rate, not by variation in development time. We conclude with a discussion of the plausible explanations for the presence of genetic variation in growth rate in this natural population.     

Reproductive biology of the brown smoothhound shark Mustelus henlei,in the northern Gulf of California,México

Female brown smoothhound sharks Mustelus henlei were found to reproduce annually. A mature female carried both developing oocytes in the ovary and developing embryos in the uteri concurrently for c. 1 year. A great variability in the size of embryos was recorded each month, and the maximum embryo sizes were found from late January to mid‐March. The largest oocytes in mature females were observed in mid‐March. Gestation lasted c. 10 months. A linear relationship between maternal total length (L_T) and the number of pups per litter (litter size one to 21) was estimated. Birth L_T was reached in c. 280 mm. Females and males matured at 570–660 and 550–560 mm L_T, respectively. Difference in the litter size among Californian coast (one to 10) and northern Gulf of California (one to 21) populations existed for this smoothhound shark.     

Sexual bimaturation and sexual size dimorphism in animals with asymptotic growth after maturity

Many animal taxa exhibit a positive correlation between sexual size dimorphism and sex differences in age at maturity, such that members of the larger sex mature at older ages than members of the smaller sex. Previous workers have suggested that sexual bimaturation is a product of sex differences in growth trajectories, but to date no one has tested this hypothesis. The current study uses growth-based models to study relationships between sexual size dimorphism and sexual bimaturation in species with asymptotic growth after maturity. These models show that sex differences in asymptotic size would produce sexual bimaturation even if both sexes approach their respective asymptotic sizes at the same age, mature at the same proportion of asymptotic size and have otherwise equivalent growth and maturation patterns. Furthermore, our analyses show that there are three ways to reduce sexual bimaturation in sexually size-dimorphic species: (1) higher characteristic growth rates for members of the larger sex, (2) larger size at birth, hatching or metamorphosis for members of the larger sex or (3) smaller ratio of size at maturity to asymptotic size (relative size at maturity) for members of the larger sex. Of these three options, sex differences in relative size at maturity are most common in size-dimorphic species and, in both male-larger and female-larger species, members of the larger sex frequently mature at a smaller proportion of their asymptotic size than do members of the smaller sex. Information about the growth and maturation patterns of a taxon can be used to determine relationships between sexual size dimorphism and sexual bimaturation for the members of that taxon. This process is illustrated for Anolis lizards, a genus in which both sexes exhibit the same strong correlation (r 0.97) between size at maturity and asymptotic size, and in which the relative size at maturity is inversely related to asymptotic size for both sexes. As a result, sexually size-dimorphic species of anoles exhibit the expected pattern of a smaller relative size at maturity for members of the larger sex. However, for species in this genus, sex differences in the relative size at maturity are not strong enough to produce the same age at maturity for both sexes in sexually size-dimorphic species. Members of the larger sex (usually males) are still expected to mature at older ages than members of the smaller sex in Anolis lizards.     

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.     

Changes in growth and maturation parameters of Pacific sardine Sardinops sagax collected off California during a period of stock recovery from 1994 to 2010

Whether fluctuation in density influenced the growth and maturation variables of three aggregated cohorts (fish born during the 1986–1993, 1996–2003 and 2004–2008 periods) of Pacific sardine Sardinops sagax caeruleus collected off the Californian coast from 2004 to 2010 was investigated. Using a von Bertalanffy mixed‐effects model with aggregated cohorts as covariates, estimated growth rate significantly covaried with aggregated cohorts. Growth rate (K) was modelled as a fixed effect and estimated to be 0·264 ± 0·015 (±s.e ). Statistical contrasts among aggregated cohorts showed that the 1996–2003 cohorts had a significantly lower growth rate than the other two aggregated cohorts. The theoretical age at length zero (t₀) and the standard length at infinity (L_S∞) were modelled as random effects, and were estimated to be ?2·885 ± 0·259 (±s.e ) and 273·13 ± 6·533 mm (±s.e ). The relation of ovary‐free mass at length was significantly different among the three aggregated cohorts, with the allometric coefficient estimated to be 2·850 ± 0·013 (±s.e ) for the S. sagax population. The age‐at‐length trajectory of S. sagax born between 1986 and 2008 showed strong density dependence effects on somatic growth rates. In contrast to the density‐dependent nature of growth, the probability to be mature at‐size or at‐age was not significantly affected by aggregated cohort density. The size and the age‐at‐50% maturity were estimated to be 150·92 mm and 0·56 years, respectively. Stock migration, natural fluctuations in biomass and removal of older and larger S. sagax by fishing might have been interplaying factors controlling growth parameters during 1986–2010.     

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.     

Patterns of reproduction in two populations of pumpkinseed sunfish,Lepomis gibbosus,with differing food resources

Synopsis The influence of available food resources on growth and patterns of reproduction was studied in two populations of pumpkinseed sunfish in adjacent lakes in southeastern Ontario. Ideally, mature individuals should be long-lived, attain a large size, and maintain a high reproductive effort. However, rarely are environmental conditions ideal and compromises are necessary. In the present study, there were smaller quantities of preferred prey items (gastropods), and total benthos available in one lake. Pumpkinseed in this population ate less in general, and were smaller in body size in the older age classes. These fish matured at a younger age and a smaller size than individuals in the other lake studied, and in populations in this geographic area reported in the literature. In addition, the relationships of both fecundity and ovary weight to total weight were different between lakes. Mean ovary weight, ripe egg size and lifetime fecundity were less in the population of small-bodies fish. Variation in patterns of reproduction between populations suggests that fish may be able to fine-tune responses to local environmental conditions.     

Reproductive biology of the fat snook Centropomus parallelus Poey, 1860 (Teleostei,Centropomidae) and implications for its management in the southern Atlantic Ocean

The reproductive biology of Centropomus parallelus was described from 589 individuals captured in estuarine and coastal waters in Southern Brazil. Length-frequency distribution showed the dominance of males in smaller length-classes (132–290 mm L_T), whereas females were dominant in larger length-classes (>290 mm L_T). Total length at maturity (L₅₀) was 180 mm L_T and corresponded to 29% of the maximum length recorded. Histological sections revealed one hermaphrodite (205 mm L_T) and few immature females. Life history traits provided herein can contribute to sustainable fisheries management practices.     

Size‐dependent reproductive success of wild zebrafish Danio rerio in the laboratory

Size‐dependent reproductive success of wild zebrafish Danio rerio was studied under controlled conditions in the laboratory to further understand the influence of spawner body size on reproductive output and egg and larval traits. Three different spawner size categories attained by size‐selective harvesting of the F₁‐offspring of wild D. rerio were established and their reproductive performance compared during a 5 day period. As to be expected, large females spawned more frequently and had significantly greater clutch sizes than small females. Contrary to expectations, small females produced larger eggs when measured as egg diameter with similar amounts of yolk compared to eggs spawned by large spawners. Eggs from small fish, however, suffered from higher egg mortality than the eggs of large individuals. Embryos from small‐sized spawners also hatched later than offspring from eggs laid by large females. Larval standard length (L_S)‐at‐hatch did not differ between the size categories, but the offspring of the large fish had significantly larger area‐at‐hatch and greater yolk‐sac volume indicating better condition. Offspring growth rates were generally similar between offspring from all size categories, but they were significantly higher for offspring spawned by small females in terms of L_S between days 60 and 90 post‐fertilization. Despite temporarily higher growth rates among the small fish offspring, the smaller energy reserves at hatching translated into lower condition later in ontogeny. It appeared that the influence of spawner body size on egg and larval traits was relatively pronounced early in development and seemed to remain in terms of condition, but not in growth, after the onset of exogenous feeding. Further studies are needed to explore the mechanisms behind the differences in offspring quality between large‐ and small‐sized spawners by disentangling size‐dependent maternal and paternal effects on reproductive variables in D. rerio.     

Reproduction of Micropogonias funieri in a shallow temperate coastal lagoon in the southern Atlantic

The white croaker Micropogonias furnieri , in the coastal Rocha Lagoon, spawned during 5 months, in late spring and summer. It was eurythermic (gonad growth at 12·5 to 25·5° C, spawning at 20 to 27° C) and mesoxic (living at 5·2 to 9·1 mg l^-1). The spawning occurred in brackish (8–18 salinity), basic ( c . 8 pH) and oxygenated ( c . 8·0 mg l^-1) waters. The temperature appeared to be an important environmental factor affecting the timing of reproduction. The size at first maturity (19–20 cm) was 11–12 cm lower than the reported for the Río de la Plata spawning area (Uruguay). Juveniles were observed throughout most of the year suggesting that the lagoon is also a nursery area. In Brazil, M. furnieri spawns in marine areas while in Uruguay it spawns in estuaries. This is the first time that a coastal lagoon of the subtropical and temperate western coast of the South Atlantic Ocean has been shown to be a spawning area of a marine species.     

Egg size manipulation: a technique for investigating maternal effects on the hatching characteristics of herring

A technique was developed for manipulating egg size of recently fertilized Atlantic herring Clupea harengus embryos. Larvae hatching from eggs with reduced yolk volume were shorter than predicted for the volume of yolk removed. The reduction in both body and yolk mass of hatchlings was less than predicted, partly because larval yolk-sac mass was unaffected by yolk removal.     

Distribution and reproduction of the southern lantern shark from New Zealand

Distribution, population structure and reproduction are described for the southern lantern shark Etmopterus granulosus at the Chatham Rise, New Zealand. Depth of capture for E. granulosus ranged from 744 to 1420 m, with highest catch rates between 800–1200 m. More than twice as many females as males were captured, and the majority of sharks caught were mature, indicating that there may be segregation according to sex and size class. Only 10 of 492 female sharks captured contained ova in uteri, and none contained embryos. The absence of pregnant females suggests that they move to another area or depth prior to pupping. Size of sharks captured ranged from 20·0 to 78·8 cm total length. Females began to mature at 62 cm total length, and males at 52 cm. There was no evidence of a seasonal reproductive cycle. Ovulation appeared to occur when ova reached a diameter of 40–45 mm. The average number of ova in mature females was 12·7. This information is crucial for assessing the impact of fisheries on E. granulosus populations.     

Tooth crown size differences between age groups: A possible new indicator of stress in skeletal samples

Juveniles and adults from a prehistoric Amerindian skeletal series from Tennessee are compared for differences in the means and variances of the buccolingual dimensions of their permanent teeth. While there are no significant differences in variance, it is found that juveniles exhibit significantly smaller mandibular canines, first premolars, and first molars. The results are similar to those of a previous examination of an Amerindian skeletal collection from South Dakota. There is evidence to suggest that teeth may fail to develop to their maximum genetic size potential when there is interference from exogenous chronic stressors such as malnutrition or disease. Archeological and biological evidence demonstrates that both the Tennessee and South Dakota series represent groups that suffered considerably from environmental stressors. It is suggested that those persons who suffered most were more likely to die prematurely, thus explaining why juvenile skeletons tend to have smaller teeth. The conclusion is that the examination of age variation in crown size can be a useful supplement to other osteological indicators of stress in skeletal collections. The factor of sex ratio and the implications of the results for other kinds of dental metric studies are discussed.     

Reproductive strategies of smooth-head catfish Clarias liocephalus (Boulenger, 1898), in the Rwizi-Rufuha wetland system,south-western Uganda

The reproduction of the smooth-head catfish (Clarias liocephalus), a heavily exploited wetland fish in Uganda, in a data-deficient fishery, was studied from January to December 2011. Analyses were based on a sample of 854 fish specimens obtained from a chain of wetlands that fringe the Rwizi River, a tributary of the Nile River. Samples were collected monthly from four sites. Fecundity, gonadosomatic index, size at sexual maturity, condition factor and growth patterns were used to describe the reproduction of the species. Mean female fecundity was 2 484.03 ± 1 289.90 (range 266–3 474). Females attained sexual maturity at a smaller size (12.0 cm TL) than males (13.79 cm TL), but were in better condition than males. Gonadosomatic index peaked in the wettest months of the study period, with highest proportion of mature ova occurring during July to November. Although C. liocephalus seems less fecund than other known clariids and is therefore prone to adverse effects from overexploitation, knowledge of its spawning periodicity and its size at sexual maturity could be useful in the management of the fishery in wetlands where it is still abundant.     

Sea growth, smolt age and age at sexual maturation in Atlantic salmon

Relationships between growth at sea, smolt size and age at sexual maturation of Atlantic salmon Salmo salar were tested. The fish were offspring of brood stocks sampled in eight Norwegian rivers at latitudes between 59° and 70° N, hatchery reared and released at smolting at the mouth of the River Imsa (59° N). Smolt size influenced the subsequent growth rate of Atlantic salmon. The larger the fish were at release, the slower the yearly length increment at sea. Mean sea age at sexual maturity, measured as proportion of the returning adults attaining sexual maturity at sea age 2 years, was significantly correlated with mean growth rate during the first year at sea and mean smolt size ( r ²= 0·74, P < 0·001). Fish attaining maturity at a relatively high sea age were more fast growing during their first year at sea than those maturing at a younger age. The results indicate that high sea age at sexual maturation is a population-specific characteristic and associated with high early growth rate at sea.     

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.