Size and age at sexual maturity of Atlantic argentine,Argentina silus: a critique

Synopsis A recent analysis of size and age at sexual maturity ofArgentina silus on the Scotian Shelf is invalid because field maturity stage data collected during the non-spawning, quiescent stage of the reproductive cycle were unreliable for distinguishing between immature and resting mature stages. Thus two-thirds of the data used must be discounted. Utilization of different length measurement criteria for different years, for which no correction is made, could introduce substantial error in length at maturity estimates based on the remaining data. Age data collections were restricted to one 12 month period and thus were inadequate to characterize age at maturity by 5 yr time periods as attempted in this analysis. No attempt is made in the analysis to determine whether available samples adequately represent the population with regard to maturity i.e. whether immature and mature fish of the same length had an equal probability of being sampled. It is demonstrated here that maturity ogives can differ greatly depending on assumptions made concerning the representativeness of samples. Many of the criticisms made are likely valid for a series of papers on maturity of Atlantic coast fishes by the same author.     

Marine post-smolt growth and age at maturity of Atlantic salmon

The annual variation in sea-age of maturation for a hatchery dependent stock of Atlantic salmon was compared to variation in post-smolt growth as evidenced by circuli spacing patterns. The proportion of returns of 1-seawinter (1 SW) and 2 SW salmon and the fraction of the smolt year class or cohort that maturated as 1 SW fish, were compared to seasonal growth indices determined from circuli spacing on the scales of smolt class survivors returning as 1 SW and 2 SW spawners. Using image processing techniques, we extracted inter-circuli distances from scales from 2244 recaptured fish. Spacing data for the first year at sea were collected and then expressed as seasonal growth indices for the spring period, when post-smolts first enter the ocean; the summer, when growth appears maximal; and winter, when growth appears to be at a minimum. In general, circuli spacings were wider for 1 SW than for the 2 SW returns of the same smolt cohort. The 1 SW fraction was significantly and positively correlated with late summer growth, suggesting that growth during this season is pivotal in determining the proportion of a smolt class that matures early.     

Variation in reef associated assemblages of the Lutjanidae and Lethrinidae at different distances offshore in the central Great Barrier Reef

Synopsis Fish traps were used to quantify the distribution and abundance of the Lutjanidae and Lethrinidae on reefs across the central Great Barrier Reef. The assemblages of fishes on inshore reefs were distinctive from those on midshelf and outershelf reefs. There were significantly fewer individuals of the Lutjanidae and Lethrinidae inshore and all species examined displayed significant cross-shelf changes in abundance. These significant cross shelf changes in abundance were due to an absence or low abundance of individuals of a species at one or more cross shelf locations, with many species present in only one location on the continental shelf. The genera Aprion, Lutjanus, Macolor, Symphorichthys, Symphorus, Gnathodentex, Gymnocranius, Lethrinus and Monotaxis were all characteristic of the shallow shelf waters less than 100 m. In contrast, species of the genera Paracaesio, Pristipomoides and Wattsia were characteristic of the intermediate depths (100–200 m) and the deeper outer reef slope waters in excess of 200 m were characterised by species of the genus Etelis.     

Growth and age at sexual maturity of South American sea lions

The average age at sexual maturity (ASM) is an important parameter for evaluating the reproductive potential or status of a population. South American sea lions, Otaria flavescens in Patagonia (Argentina) were exploited and reduced to less than 10% of pre-exploitation numbers. At present, the population is recovering at a rate of 6%. In this paper, we studied growth and age at sexual maturity of South American sea lions in the south-western south Atlantic by examining 219 individuals (females and males) collected between 1989-2008. Individuals were aged by counting growth layer groups in tooth sections, standard body length was measured and male and female reproductive organs were examined macroscopically and histologically to establish individual sexual maturity. Maximum recorded length for males and females was 264 cm and 200 cm, respectively, and maximum ages 19 and 21 yrs. ASM defined as the age where 50% of females are mature, was estimated at 4.8±0.5 years old, corresponding to a mean SL of 147 cm, about 81% of their asymptotic length. First observed ovulation occurred during the 4th year, first birth may occur between 4 and 5 years old. Males physiologically mature between 4-6 years, but the size of the testes shows that all males became sexually mature by the age of 9 years when they reach a mean SL of 212 cm, about 86% of their asymptotic body length. The present information on ASM and growth of O. flavescens will improve the development of population dynamics models, to investigate the impact of recovering sea lions populations on its marine environment, as well as its trophic interactions with commercial fisheries.     

Father absence predicts age at sexual maturity and reproductive timing in British men

Despite the widespread assumption that paternal investment is substantial in our species, previous studies have shown mixed results in relation to the impact of fathers on both offspring survival and reproductive outcomes. Using data from a large representative sample of British men, we tested whether father absence is associated with the timing of reproduction-related events among boys, while controlling for various cues denoting early childhood adversity. We further tested whether the loss of the father at different childhood stages matters, so as to assess whether early life is the most important period or if effects can be seen during later childhood. The results show that father absence before age seven is associated with early reproduction, while father absence between ages 11 and 16 only is associated with delayed voice-breaking (a proxy for puberty), even after adjusting for other factors denoting childhood adversity. We conclude that fathers do exert an influence on male reproductive outcomes, independently of other childhood adversities and that these effects are sensitive to the timing of father absence.     

Phenotypic plasticity of life-history traits in clonal and sexual fish (Poeciliopsis) at high and low densities

Models of resource allocation strategies predict an array of life-history responses of individuals living in resource-stressed versus non-stressed environments. I tested a number of these predictions using three fish strains (a sexual and two clonal strains) in high and low density treatments. To examine the plasticity of life-history traits in females raised in these two environments, I measured survival, growth, egg production, egg size, and proportion mature at 10 weeks of age. Survival was not affected by density treatment. However, both growth and overall egg production were lower in females from the high density treatments, and reproductive maturity was significantly delayed at the high density for all strains. Egg production per unit size was not affected by density in any strain, signifying that differences in the numbers of eggs produced was merely a reflection of the differences in size of fish in the two density treatments. Egg size was also unaffected by density in all strains. These results are related to models of resource allocation in stressful environments. There was a consistent pattern of increased reproductive investment in the sexual strain relative to the two clonal strains. The sexual strain matured earlier, produced more eggs per unit body weight, and had larger eggs than either clone at both densities. These results are interpreted by considering the predicted adaptive responses of these three strains to the long-term environmental differences in their natural habitats.     

Temporal changes in fecundity and age at sexual maturity of southern elephant seals at Marion Island

Our objective was to examine the effect of variation in reproductive parameters on the demography of southern elephant seals at Marion Island. We used age-specific capture probabilities of breeding females in a Cormack-Jolly-Seber context to derive reproductive rates. We found that age at maturity declined and fecundity rates increased as the population declined, indicating a compensatory response. Fecundity rates ranged from 0.03 to 0.29 among 3-year-olds (mean=0.16), 0.18 to 0.50 in 4-year-olds (mean=0.40), and 0.28 to 0.50 in 5-year-olds (mean=0.45). We think that a relative increase in food availability, concomitant with the population decline, promoted earlier sexual maturity correlated with more rapid growth of juveniles when population abundance was lower. It is suggested that the relative importance of fecundity in population regulation in elephant seals has been underestimated. Moreover, it appears that the onset of sexual maturity may be the first demographic variable to change in response to a change in population density.     

Age and length at maturity of the female spiny dogfish,Squalus acanthias,in the Strait of Georgia,British Columbia,Canada

Synopsis A total of 3068 female spiny dogfish were examined to determine the age and length at maturity. The median age at maturity for females was 35.5 years with 95% confidence limits between 35.0 and 35.9 years. It was found that slower growing dogfish tended to mature at a smaller size. A deterministic model incorporating fecundity, growth and reproduction was used to examine the reproductive style of spiny dogfish. The age at maturity reported corresponds to the level that theoretically maximizes lifetime reproductive output for a cohort.     

The relationship between body length, age and sexual maturity in the common toad, Bufo bufo

An investigation of the relationship between the onset of sexual maturity, age and body size in common toads Bufo bufo was started in 1984 at a pond in southern England. During the toad breeding seasons of 1984 and 1985, 7259 common toad'metamorphs'were captured and permanently marked so that if captured as adults their true age would be known. Although a very small proportion of males and females reached sexual maturity at ages of two and four years respectively, most did so much later and asynchronously. The body size of toads breeding for the first time was relatively constant for each sex and not correlated with age. The rational behind our understanding of the mechanism of female choice is discussed in the light of these results.     

Social organization and spawning in the Atlantic sharpnose puffer,Canthigaster rostrata (Tetraodontidae)

Synopsis Social organization and spawning in the sharpnose pufferCanthigaster rostrataere studied on a reef in the San Blas Islands, Panama. Sexes were dimorphic. In mixed coral and rubble habitat, females defended territories against other females and small males. From one to six female territories were included within the territories of certain large males. These haremic males visited their females and patrolled their territories throughout the day. Smaller, non-haremic males occupied territories or home ranges within or adjacent to those of haremic males or were wanderers. Spawning between a haremic male and a territorial female occurred within the female's territory. The female prepared an algal nest into which demersal eggs were deposited. There was no parental care. Eggs were spherical, translucent, and measured approximately 0.66 mm in diameter. Larvae were about 1.4 mm TL and closely resembled those of other species ofCanthigaster.     

Disturbance and organization of macroalgal assemblages in the Northwest Atlantic

Large seaweeds are often structurally dominant in subtidal and intertidal rocky shore benthic communities of the N.W. Atlantic. The mechanisms by which these algal assemblages are maintained are surprisingly different in the two habitats. In the subtidal community, kelps are dominant space competitors in the absence of strong grazing interactions. In contrast, the large perennial seaweeds of intertidal zones (fucoids and Chondrus crispus) are competitively inferior to both sessile filter feeders and ephemeral, pioneer algal species. Intertidal seaweed beds are maintained by carnivory of whelks, which reduces filter feeder populations, and by herbivorous periwinkles which reduce ephemeral algal populations. Through most of the intertidal zone, disturbance, both biological and physical, dictates which species shall compete and equilibrium conditions obtain subsequently.The roles of subtidal consumers are quite different. Sea urchins are the major algal herbivores and these voracious animals maintain an equilibrium state in which large tracts of subtidal coralline pavement are kept free of kelp forests. Urchins do not seem to play a successional facilitative role for kelps in the way that periwinkles do for fucoids in the intertidal. Control of herbivore populations is thus a key to the maintenance of subtidal foliose algal beds. It is clear that parasitic amoebas can decimate sea urchin populations so that kelp forest dominance is assured. However, the importance of carnivory in limiting urchins in the subtidal community is unclear in the absence of appropriate manipulation experiments. It is possible that carnivorous decapods and fin fish control sea urchin populations and hence foliose algal abundance, but this must remain speculative. The seaweed-dominated state of the subtidal system is an alternative equilibrium condition to the urchin/coralline alga configuration. The structure of the kelp beds is relatively uniform in responding to frequent small-scale, infrequent large-scale, or no, disturbance.     

Spain,the European Union,and Canada: A New Phase in the Unstable Balance in the Northwest Atlantic Fisheries

The past stormy fisheries relations between Canada and the European Union, in particular with Spain, has been replaced by uncertainty in the application of the newly amended Northwest Atlantic Fisheries Convention. These issues are addressed in this article that sheds light on the more peaceful fishing relations between the two leading international actors in this area of the oceans.     

Bimodal size distributions in wild juvenile Atlantic salmon populations and their relationship with age at smolt migration

A bimodal length distribution developed in an Atlantic salmon population planted as start-fed fry in a Norwegian stream. The earliest fish to smolt were from the upper modal group.     

Effects of sexual differences of age at maturity and survival on population sex ratio

Summary Five demographical factors influencing the sex ratio of a population are classically considered. The influence of two of them is dependent on the longevity of individuals in the population. The effect of differential age at maturity between males and females is higher for animals with low annual survival, whereas the effect of differential annual survival between males and females is higher for animals with high annual survival. Such a conclusion applied to turtles, which are long life-span animals, allows us to retain differential survival between sexes as a major factor influencing the population sex ratio.     

Density-dependent growth and sexual maturity of silver hake in the north-west Atlantic

Stock abundance was the most important predictor of sexual maturation of age 2 and 3 silver hake in the north-west Atlantic between 1973–1990. Growth at ages 1 and 2 in the southern stock was significantly and negatively correlated with stock abundance (r²>0.56, P <0.01). Sexual maturity may be mediated through competition and growth during the first and second years of life. In the northern stock, growth and stock abundance was not significantly correlated ( P >0.05). Here, increased sexual maturity at ages 2 and 3 during 1973–1990 may have occurred without increased somatic growth, already near its maximum, due to the relatively cooler water temperatures of the Gulf of Maine. Logistic regression models indicated that maturation is dependent on age, stock density and an age-density interaction.     

The North Atlantic Oscillation and plankton dynamics in two European lakes –- two variations on a general theme

Long‐term data on water temperature, phytoplankton biovolume, Bosmina and Daphnia abundance and the timing of the clear‐water phase were compared and analysed with respect to the influence of the North Atlantic Oscillation (NAO) in two strongly contrasting lakes in central Europe. In small, shallow, hypertrophic Müggelsee, spring water temperatures and Daphnia abundance both increased more rapidly than in large, deep, meso/oligotrophic Lake Constance. Because of this, the clear‐water phase commenced approximately three weeks earlier in Müggelsee than in Lake Constance. In Müggelsee, the phytoplankton biovolume during late winter/early spring was related to the NAO index. In Lake Constance, where phytoplankton growth was inhibited by intense downward mixing during all years studied, this was not the case. However, in both lakes, interannual variability in water temperature, in Daphnia spring population dynamics and in the timing of the clear‐water phase, were all related to the interannual variability of the NAO index. The Daphnia spring population dynamics and the timing of the clear‐water phase appear to be synchronized by the NAO despite large differences between the lakes in morphometry, trophic status and flushing and mixis regimes, and despite the great distance between the lakes (～700 km). This suggests that a great variety of lakes in central Europe may possibly have exhibited similar interannual variability during the last 20 years.     

Optimal age at sexual maturity of sympatric and experimentally allopatric cutthroat trout and Dolly Varden charr

Summary Reproductive potentials of transplanted curthroat trout (Salmo clarki) and Dolly Varden charr (Salvelinus malma) and of their donor stocks were estimated from life history data. We found good agreement between observed and predicted age at maturity in all populations, and cannot reject the hypothesis that the fish matured at the age maximizing the overall lifetime reproductive potential ( ). Our estimates were insensitive to probable variations in female fecundity, adult mortalityrate and maximum body length. Small changes in either juvenile mortality-rate or individual growth-rate had marked effects on the estimations, as did changes in the Malthusian parameter (r). Three alternative mechanistic explanations of how age at maturity is determined could be rejected. We suggest that fish are able to adjust the maturity age non-genetically to changes in growth-rate, and that temporal variations in juvenile survival-rate allow coexistence of genotypes coding for different ages at maturity at the same growth-rate.     

Optimal age of sexual maturity and limitations of juvenile survival in mammals

Although the life history evolution of small- and large-bodied mammals seems to be governed by different factors, the both shows relative neonate size and juvenile survival to be slightly dependent on body mass. I propose a hypothesis that natural selection simultaneously maximizes a time to maturity (minimizes somatic growth rate) and a number of newborn survived to reproduction. In this case optimal juvenile survival of large-bodied mammals must be close to e-beta and that of small-bodied approximately e-(1 + beta), where beta is the slope of the regression of log annual fecundity on log annual juvenile mortality. Analysis of vital characters for 71 mammal species revealed the slope to be close to unity. As a result frequency distribution of log juvenile survival shows bimodality which coincides well with predicted optimal survival for large- and small-bodies species. It is shown that the relative neonate size can be directly proportional to the juvenile survival and inversely proportional to the lifetime offspring production irrespective of mortality factors.     

Induction of vitellogenin synthesis in an Atlantic salmon (Salmo salar) hepatocyte culture: a sensitive in vitro bioassay for the oestrogenic and anti-oestrogenic activity of chemicals

A variety of organic compounds have been documented to bind to the oestrogen receptor and induce oestrogenic effects in different vertebrates. The presence of these environmental oestrogens or oestrogen mimics in the aquatic environment has been suspected of disrupting the normal endocrinology of wild populations of fish. In this study, induction of vitellogenin synthesis in primary hepatocytes from Atlantic salmon (Salmo salar) was optimized and validated as an oestrogenic in vitro bioassay using a sensitive capture vitellogenin enzyme-linked immunosorbent assay. After proper optimization (cell media supplements, cell density, temperature and exposure time), this assay gave a sensitive and reproducible response to both endogenous steroids (relative potency: 17β-oestradiol?oestriol>oestrone>17α-oestradiol) and a range of common oestrogen mimics (relative potency: ethynyloestradiol and diethylstilboestrol?genistein and zearalenone?bisphenol A and 4-t-octylphenol>4-n-nonylphenol and 2′-chloro,4-chloro-diphenyltrichloroethane (o,p′-DDT). However, the androgen testosterone and the putative oestrogen mimics dieldrin and toxaphene were not shown to be oestrogenic using this hepatocyte bioassay. Oestrogen-induced vitellogenin synthesis was efficiently inhibited by the anti-oestrogen ZM 189.154, suggesting that this bioassay may be used for testing both the oestrogenic and the anti-oestrogenic properties of chemicals.