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.     

Traditional approaches to estimate length at first maturity (L50) retrieve better results than alternative ones in a Neotropical heptapterid

Length at first maturity (L₅₀) is an important tool for the management and conservation of fish populations. Traditional approaches based on macroscopic and microscopic maturity staging exhibit high accuracy and precision, while alternative approaches (e.g., I_g-based staging, stanza changing point) are less resource-demanding. Herein, we compare four approaches to estimate L₅₀ in a population of the heptapterid Rhamdioglanis transfasciatus from Atlantic Forest streams. Fish were sampled monthly during a year by using electrofishing. We measured the length (cm), mass (g), and gonad mass (g) of each specimen, then classified their maturity status macroscopically and microscopically. Alternative approaches were strongly discordant from traditional ones. Logistic curves considering mature individuals as those displaying at least 1% of the maximum I_g in the sample greatly underestimated L₅₀ for females and overestimated L₅₀ for males. The stanza changing point derived from the polyphasic growth model underestimated L₅₀ in both cases. Despite the increasing development of less onerous approaches, it seems that they are not suitable for all fish populations and the requirements to use such approaches demand further investigation.     

Adolescence and the Reversibility of Maturity in Euplotes crassus

ABSTRACT. The clonal life history of ciliated protists is characterized by a sequence of phenotypes; sexual immaturity, maturity, and senescence. The distinctiveness of immaturity and maturity has been investigated. Standard assays of the onset of maturity of progeny clones from a cross between stocks EC1 and EC2 of Euplotes crassus demonstrated significant differences among clones and among testers within clones. They also revealed that the first positive test(s) of a progeny subclone were typically followed by at least one negative test. Special protocols were devised to investigate if maturity was reversible at the cellular level. In these experiments, the first mating pair of a progeny subclone was split before the consummation of mating. From these two cells as well as from control progeny and tester cells, subclones were established and every leftover cell was tested for maturity after each transfer. Both standard and split-pair progeny subclones had immature and slow- to-mate cells. The number of fissions before progeny exhibited sexual behavior indistinguishable from the testers was more than twice that to the first mating reaction of a subclone. At the first sign of maturity, progeny lines are a heterogeneous population of cells able and not able to mate, but remarkably, clonal descendants of those able to mate may become unable to mate. The development of maturity is progressive, quantitative and non-monotonic rather than an instantaneous switch.     

Age at maturity of some fish species distributed in Turkish marine waters (Actinopterygii and Elasmobranchii)

We collected data on the age at maturity (t_m) and maximum reported age (t_max) for 153 stocks of marine fishes in Turkey, belonging to 59 species, 24 families and 2 classes (Actinopterygii and Elasmobranchii). Among Actinopterygii t_m had an average of 1.8 years (1 to 4 years) while among Elasmobranchii it had an average of 11.9 years (2 to 11.9 years). Overall, t_max ranged between two years (for Sarda sarda) and 34 years (for Squalus acanthias). Mean t_max was found to be 6.24 years for Actinopterygii and 10.11 years for Elasmobranchii. t_m showed a positive linear correlation with t_max for both Actinopterygii and Elasmobranchii. Mean t_m?t_max did not differ significantly with sex within the Actinopterygii and Elasmobranchii. The ratio t_m?t_max was found to be significantly lower for Actinopterygii than for Elasmobranchii.     

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.     

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.     

Life-history responses of a mayfly to seasonal constraints and predation risk

Abstract. 1. An experiment was conducted in the laboratory to examine the effects of photoperiod and predation risk on life-history variation in the mayfly Ephemerella subvaria .
2. Both photoperiod and predation risk affected age at maturity significantly but neither factor affected size at maturity. Mayflies perceiving themselves to be late in the growing season matured in fewer days than those perceiving themselves to be early in the growing season. The presence of predators delayed mayfly maturity significantly.
3. These results suggest that the large variation in life-history traits observed in aquatic insects may be attributed partially to seasonality but that other biotic and abiotic factors may also underlie variation in these traits.     

Natural selection on age of maturity in shrimp

Summary Darwinian fitness with respect to the age of maturity () in stationary populations can be written as the product of two functions: pre- survival times the Fisherian reproductive value of an age (a just mature) individual. This reduces normalizing selection on to the maximization of a simple product,a twodimensional problem (Charnov in press). I apply this products theorem to in Pandalid shrimp and compare the results to previous analysis (Roff, 1986) of in fish.     

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.     

Distribution, reproduction and feeding of the Greenland shark Somniosus (Somniosus) microcephalus, with notes on two other sleeper sharks, Somniosus (Somniosus) pacificus and Somniosus (Somniosus) antarcticus

The size and depth distribution, stomach contents and reproductive status of Somniosus ( Somniosus ) microcephalus, Somniosus ( Somniosus ) pacificus and Somniosus ( Somniosus ) antarcticus were examined from specimens collected from the North and South Atlantic, North and South Pacific, and the Southern Ocean. Specimens ranged in size from 42 to 480 cm total length, L _T, and were taken from depths of 35–1280 m. Stomach contents included coelenterates, gastropods, cephalopods, echinoderms, crustaceans, elasmobranchs, teleosts, penguins, marine mammals and human waste. Female S. ( S. ) microcephalus mature at c . 450 cm and S. ( S. ) antarcticus at c . 435 cm L _T; a female S. ( S. ) pacificus of 430 cm was mature. Male S. ( S. ) microcephalus mature at c . 300 cm, but male S. ( S. ) antarcticus may not mature until c . 400 cm L _T. The size at birth in these three species of Somniosus is c . 40 cm L _T.     

New data on the reproductive biology of the thorny stingray,Dasyatis centroura (pisces: Dasyatidae) from off the Tunisian coasts

Synopsis Aspects of the reproductive biology are described for the thorny stingray,Dasyatis centroura, caught off the coasts of Tunis, mainly from the Gulfs of Gabes and Tunis. Sexual maturity in males occurs at a disk width (DW) of 800 mm. Female maturation occurs between 660 mm and 1000mm DW All males and females having a DW greater than 800 and 1000mm, respectively, were adults. Females are larger than males, with adult specimens having an average DW of 1040mm in males and 1345mm in females. Gestation lasts for a minimum of about 4 months. The number of reproductive cycles per year is unknown. Vitellogenesis is completed at the end of the gestation. Parturition and ovulation occur in June. Fecundity ranges from 2 to 6 individuals per litter.     

Reproductive parameters of clouded leopards (Neofelis nebulosa)

Reproductive data compiled from the International Clouded Leopard Studbook revealed that 75% of all litters were born to females between one and five years of age. Sixty-three percent of the males had sired litters by four years of age with reproduction declining after six years of age. Sixteen zoological institutions surveyed worldwide contributed estrous cycle data from 28 clouded leopards. Sexual maturity (age at first estrus) for these females ranged from 17 to 28 months of age with a mean estrous cycle length of 29.9 ± 13.8 days. The mean length of estrus was six days. Gestation length ranged from 85 to 121 days (X? = 93.4 ± 6.3). There was a significantly higher incidence of estrus in fall and winter compared with spring and summer over latitudes ranging from 36°–45° and 51°–55° (P < .005). Mating occurred in all months except June and October, and cubs were produced in all months except December. The highest frequency of mating occurred during the month of December corresponding with a birth peak in March.     

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.     

Sexual and developmental differences in the protein pattern of haemolymph and body tissues of Streptocephalus dichotomus Baird (Crustacea: Anostraca)

The protein pattern of haemolymph and body tissues of the freshwater fairy shrimp Streptocephalus dichotomus has been investigated in both sexes, using polyacrylamide disc gel electrophoresis. The electropherograms of four developmental stages show variations in number and intensities of protein fractions. In Stage III, two female-specific proteins of glycolipoprotein nature appear. This stage corresponds to maturity: females begin to possess mature oocytes in the ovary. These two vitellogenic proteins are well represented in the female haemolymph, ovary and freshly laid eggs, but are absent in the male haemolymph. A heterosynthetic mode of yolk formation is thus evident in this anostracan. The two sex-limited proteins are only faintly represented in shelled eggs, suggesting an early utilization of these compounds in embryogenesis.     

Early functional maturity of captive male northern elephant seals (Mirounga angustirostris)

A male northern elephant seal (Mirounga angustirostris) that was conceived in captivity was stillborn February 14, 1981, at Mystic Marinelife Aquarium in Mystic, Connecticut. Either of two males in the exhibit could have sired the pup. Both were only 3 yr at the time of conception.     

Histomorphological and endocrine assessment of female Arabian carpetshark,Chiloscyllium arabicum (Elasmobranchii: Hemiscylliidae) from the Persian Gulf during annual reproductive cycle

The present study aimed at assessing the annual reproductive cycle of female Arabian carpetshark, Chiloscyllium arabicum from the Persian Gulf by a macroscopic and microscopic evaluation of the reproductive tract. The annual cycle of gonadal steroids [17β-estradiol (E2), progesterone (P4) and testosterone (T)] was also assessed in this shark. In total, 130 female C. arabicum were collected from the Bahrakan Creek (located northwest of the Persian Gulf) between January 2018 and March 2019. Females were oviparous with an external-type ovary and only one functional ovary. Five sexual maturity stages were recognized based on macroscopic and microscopic evaluation: Immature I (August–October), Immature II (November–January), Mature (February–March), Pregnant (April–May) and Spent (June–July). The structural changes in the oviducts, oviducal glands and uterus throughout the annual reproductive cycle were consistent with their roles in the egg movement, the egg capsule production and sperm storage. The plasma levels of the gonadal steroids were associated with morphological changes in the reproductive tract. E2 showed two detectable peaks during March (close to ovulation) and June (just before mating). P4 and T displayed a peak just before ovulation.     

The influence of temperature on the onset of first maturity in sea bass

Oocyte development was aborted and full maturity did not occur in virgin female sea bass Dicentrarchus labrax unless they remained in water above 10° C during the main period of gonad development. There was no difference in the condition factors of females with high or low I _G values in March, which indicates that retarded gonadal development was not necessarily due to poor body condition or nutritional state. It is suggested that the extended duration of the adolescent phase of female bass around southern Britain is a response to their environment, rather than an intrinsic aspect of the species'biology.