The growth of the common two-banded seabream, Diplodus vulgaris (Teleostei, Sparidae), in Canarian waters, estimated by reading otoliths and by back-calculation

The yearly nature of increment formation in the otoliths of 1–9‐year‐old seabream, Diplodus vulgaris (E. Geoffrey Saint‐Hilaire 1817), from the Canary Islands was validated. The marginal increment method showed that the opaque rings were formed in summer, and the translucent rings in winter. The Brody Proportional Hypothesis and the power length–radius relationship used to back‐calculate the growth trajectories of D. vulgaris showed that this growth model could provide reasonable growth estimates in this species. Growth back‐calculation and growth estimates obtained by direct otolith readings were similar. Data on age and size used to estimate the parameters of the von Bertalanffy growth model for D. vulagris from the Canary Islands showed that males and females had similar growth rates.     

Female‐biased dimorphism in size and age at maturity is reduced at higher latitudes in lake whitefish Coregonus clupeaformis

Female‐biased sexual dimorphism in size at maturity is a common pattern observed in freshwater fishes with indeterminate growth, yet can vary in magnitude among populations for reasons that are not well understood. According to sex‐specific optimization models, female‐biased sexual size dimorphism can evolve due to sexual selection favouring earlier maturation by males, even when sexes are otherwise similar in their growth and mortality regimes. The magnitude of sexual size dimorphism is expected to depend on mortality rate. When mortality rates are low, both males and females are expected to mature at older ages and larger sizes, with size determined by the von Bertalanffy growth equation. The difference between size at maturity in males and females becomes reduced when maturing at older ages, closer to asymptotic size. This phenomenon is called von Bertalanffy buffering. The predicted relationship between the magnitude of female‐biased sexual dimorphism in age and size at maturity and mortality rate was tested in a comparative analysis of lake whitefish Coregonus clupeaformis from 26 populations across a broad latitudinal range in North America. Most C. clupeaformis populations displayed female‐biased sexual dimorphism in size and age at 50% maturity. As predicted, female‐biased sexual size dimorphism was less extreme among lower mortality, high‐latitude populations.     

Age and growth of longnose trevally (Carangoides chrysophrys) in the Arabian Sea

The ages and growth of longnose trevally (Carangoides chrysophrys), caught in the northwest Arabian Sea between April 2005 and September 2006, were investigated. Age and growth of 336 fish specimens were determined using sectioned sagittae otoliths. Annual opaque growth rings were formed between December and March, with the majority being laid down in February and March, coinciding with the spawning period and high water temperatures. Marginal zone or edge analysis was used to validate the annual deposition of the opaque zone in the otoliths. This species showed large variations in length‐at‐age, suggesting large growth variations among individuals of the same cohort. The estimated von Bertalanffy growth model differed significantly between the sexes, with males having larger mean lengths at age and reaching a larger asymptotic size. The von Bertalanffy growth models were TL (cm) = 73.34[1‐exp (?0.25 (t + 1.21))] and TL(cm) = 73.26[1‐exp (?0.24 (t + 1.20))] for males and females, respectively.     

The growth of the freshwater murrel,Ophicephalus punctatus Bloch

Summary The growth of O. punctatus has been studied from the zones on the opercular bones and scales. Size estimates obtained from the opercular bones and scales were further substantiated by length frequency distribution and back-calculations. A close agreement in length-age relationship was obtained by various methods. These observations provide adequate evidence towards the validity of age determination in O. punctatus.Growth rate differs markedly in the two sexes. Males grow faster than the females. To study the changes in length with age, von Bertalanffy growth equation and Gompertz curve were used. The theoretical lengths obtained from the von Bertalanffy equation agreed very closely with the observed lengths.There is sexual difference in the weight-length relationship of O. punctatus. Modal weight of each year class obtained according to age reading showed that growth in weight is faster in males. The theoretical growth equation gives a good fit for weight-age data. O. punctatus is generally a fish of the impounded waters. The interrelationship between pond environment and growth characteristics has been discussed.     

The growth and age structure of Chilean jack mackerel (Trachurus murphyi) following its influx to New Zealand waters

The Chilean jack mackerel (Trachurus murphyi) is a predominantly Southeast Pacific Ocean species. It is relatively difficult to determine its age, and multiple studies of its growth off South America have produced markedly different sets of von Bertalanffy parameters. T. murphyi was first identified from New Zealand waters in the mid-1980s and has comprised part of the commercial landings of Trachurus species (along with Trachurus declivis and Trachurus novaezelandiae) since then. Results from 13 years of age determination of New Zealand samples using sectioned otoliths indicate that a partially validated age determination method has been developed, with a precision level (average percentage error) of 4.6%. The best available von Bertalanffy growth parameters for the New Zealand population (sexes combined) are as follows: L_∞, 51.9 cm fork length; K, 0.223 per year; t₀, −0.5 year. Analyses by sex showed that males have a significantly larger L_∞ than females. Estimated annual catch-at-length and catch-at-age distributions from the fishery are presented for 2007–2019. There have been at least two episodes of immigration of T. murphyi from international waters, but little evidence of spawning success to maintain the New Zealand population.     

Age and growth of black seabream Acanthopagrus schlegelii (Sparidae) in Hong Kong and adjacent waters of the northern South China Sea

Age and growth of the black seabream Acanthopagrus schlegelii (family Sparidae) from the northern South China Sea (NSCS) were studied by reading growth rings in sectioned sagittal otoliths. Ring formation frequency was determined to be annual by using marginal increment analysis. The von Bertalanffy growth function parameters were estimated as: L_∞ = 43.7 cm L_S; K =0.22 year; t₀ = ?1.59 years. Functional males are significantly younger than functional females, with sexually transitional individuals between the modal ages of males and females supporting protandry in this species. Males become sexually mature within 1 year and 50% age at sex change is at 2 years. The maximum age recorded for both males and females sampled was 9 years which is lower than for conspecifics elsewhere and may reflect high fishing pressure in the study area when compared with conspecifics in other areas or could reflect latitudinal effects. Otolith mass was significantly and positively related to age, providing a cheap and quick alternative method for approximating age. Acanthopagrus schlegelii is a relatively fast‐growing and rapidly maturing species attaining a similar asymptotic length to conspecifics. A need for fishery management is indicated to protect both young juveniles and older adults, especially females, to increase reproductive output and safeguard fishery production.     

Age and growth analysis of the shortfin mako, <Emphasis Type="Italic">Isurus oxyrinchus</Emphasis>, in the western and central North Pacific Ocean

We determined the age and growth rates of male and female shortfin makos, (Isurus oxyrinchus), from the western and central North Pacific Ocean. Growth band pairs were counted on half-cut vertebral centra using a shadowing method. In this method, we focused on the ridges on the surface of the centra, consisting of a convex and concave structure. After comparing four enhancing methods, we decided on the use of shadowing method for aging. Vertebrae from 128 males and 147 females were examined. The centrum edge analysis suggested annual band pair formation. Von Bertalanffy growth curves were fitted separately to the length-at-age data for males and females with birth length fixed. Until approximately 7 years of age, both sexes showed similar growth rates; thereafter, males showed a significantly slower growth rate compared to females. It was suggested males and females mature at approximately 6 years and 16 years, respectively. These life-history characteristics suggest relatively low productivity for this species, which agrees with reports on populations in other geographic regions.     

Age,growth, maturity and extinction risk of an exploited and endangered skate,Atlantoraja castelnaui,from off Uruguay and northern Argentina

The spotback skate Atlantoraja castelnaui (Arhynchobatidae) is a large and threatened skate species subjected to fishing pressure, endemic to the Southwest Atlantic that occurs from Rio de Janeiro, Brazil, to San Jorge Gulf, Argentina. The age, growth, age at maturity and the maximum intrinsic rate of population increase r_max of A. castelnaui were studied using 152 specimens collected from off Uruguay and north Argentina (35°–42° S), between June 2013 and February 2020. Vertebrae from 143 individuals were used for ageing (females: n = 83, size range 404–1300 mm total length, TL; males: n = 60, size range 400–1270 mm TL). Maximum ages determined for females and males were 30 and 28 years, respectively. To fit growth models, non-linear and Bayesian estimation approaches were considered. For the first approach, a set of four candidate growth (size-at-age) models were fitted: three-parameter von Bertalanffy, two-parameter von Bertalanffy with fixed L₀, Gompertz and Logistic. In the second approach, von Bertalanffy, Gompertz and Logistic were fitted. For non-linear estimation, model selection indicated that the entire set of candidate growth models were supported by the data. The von Bertalanffy was selected as the best model for Bayesian estimation. There were no differences in growth between sexes. For the sexes combined, the von Bertalanffy growth model by Bayesian method was considered the most adequate to describe the growth of A. castelnaui (growth mean parameters ± S.D. : L_∞ = 1210.29 ± 40.68 mm; k = 0.12 ± 0.01 years⁻¹; L₀ = 179.20 ± 11.62 mm). The age at maturity was estimated at 16.21 and 14.04 years for females and males, respectively. The maximum intrinsic rate of population increase r_max was estimated as 0.252 years⁻¹. Life-history traits and r_max provided in the present study suggest that this species has a relatively low productivity and may be vulnerable to an intense fishing pressure.     

Age,growth and reproductive biology of the silky shark,Carcharhinus falciformis,and the scalloped hammerhead,Sphyrna lewini,from the northwestern Gulf of Mexico

Synopsis The silky shark, Carcharhinus falciformis, and scalloped hammerhead, Sphyrna lewini, represent >80% of the shark by-catch of the winter swordfish/tuna longline fishery of the northwestern Gulf of Mexico. This catch represents a potential supplemental fishery, yet little is known of the life histories of the two species. This report relates reproductive biology data to age and growth estimates for 135 C. falciformis and 78 S. lewini. Unlike other regional populations, C. falciformis in the Gulf of Mexico may have a seasonal 12 month gestation period. Males mature at 210–220 cm TL (6–7 yr); females at >225 cm TL (7–9 yr). Application of age at length data for combined sexes produced von Bertalanffy growth model parameter estimates of L_∞ = 291 cm TL, K = 0.153, t₀ = −2.2 yr. Adult male S. lewini outnumbered adult females in catches because of differences in the distributions of the sexually segregated population. Males mature at 180 cm TL (10 yr); females at 250 cm TL (15 yr). von Bertalanffy parameter estimates for combined sexes of this species were L_∞ = 329 cm TL, K = 0.073, t_o = −2.2 yr.     

Age and growth of the sandbar shark, Carcharhinus plumbeus, in Hawaiian waters through vertebral analysis

Age and growth estimates were determined for the sandbar shark, Carcharhinus plumbeus, from Oahu, Hawaii in the central Pacific Ocean. Age estimates were obtained through vertebral centra analysis of 187 sharks. We verified our age estimates through marginal increment analysis of centra and oxytetracycline marking methods of at liberty sandbar sharks. Sizes of sampled sharks ranged from 46 to 147 cm pre-caudal length. Four growth models were fitted to length-at-age data; two forms of the von Bertalanffy growth model, the Gompertz growth model, and a logistic growth model. Males and females exhibited statistically significant differences in growth, indicating that females grow slower and attain larger sizes than males. Growth parameter estimates revealed slower growth rates than previously estimated (based on captive specimens) for Hawaiian sandbar sharks. The von Bertalanffy growth model using empirical length-at-birth provided the best biological and statistical fit to the data. This model gave parameter estimates of L _∞ = 138.5 cm PCL and k = 0.12 year⁻¹ for males and L _∞ = 152.8 cm PCL, k = 0.10 year⁻¹ for females. Male and female sandbar sharks mature at approximately 8 and 10 years of age, respectively.     

Modelling the growth of Japanese eel Anguilla japonica in the lower reach of the Kao-Ping River, southern Taiwan: an information theory approach

Information theory was applied to select the best model fitting total length ( L _T)-at-age data and calculate the averaged model for Japanese eel Anguilla japonica compiled from published literature and the differences in growth between sexes were examined. Five candidate growth models were the von Bertalanffy, generalized von Bertalanffy, Gompertz, logistic and power models. The von Bertalanffy growth model with sex-specific coefficients was best supported by the data and nearly overlapped the averaged growth model based on Akaike weights, indicating a similar fit to the data. The Gompertz, generalized von Bertalanffy and power growth models were also substantially supported by the data. The L _T at age of A. japonica were larger in females than in males according to the averaged growth mode, suggesting a sexual dimorphism in growth. Model inferences based on information theory, which deal with uncertainty in model selection and robust parameter estimates, are recommended for modelling the growth of A. japonica .     

Age and growth of the bonnethead shark, Sphyrna tiburo, from northwest Florida, with comments on clinal variation

Age and growth rates of the bonnethead shark, Sphyrna tiburo, from northwest Florida were estimated from vertebrae collected between October 1992 and October 1995. The von Bertalanffy growth equation was fit to male and female vertebral age data. Initial growth was rapid (≈ 200 mm TL) for both sexes from age 0–1. At age 2 growth slowed for males but continued for females. Similar to many species of sharks, females grew slower than males (K = 0.28 and K = 0.69, respectively) but attained a larger maximum size (L_∞=1226 and L_∞=897). Maximum age was estimated in males and females to be 8+ and 12+ years, respectively. Growth of young-of-year sharks was 21 to 30 mm TL per month determined by three different methods. A comparison of age and growth estimates from populations at more southerly latitudes suggest that clinal variation in total length may be evident among bonnethead sharks in the Gulf of Mexico with females reaching larger sizes in northern areas as compared to south Florida. This revised version was published online in July 2006 with corrections to the Cover Date.     

Growth and annual survival estimates to examine the ecology of larval lamprey and the implications of ageing error in fitting models

This study used existing western brook lamprey Lampetra richardsoni age information to fit three different growth models (i.e. von Bertalanffy, Gompertz and logistic) with and without error in age estimates. Among these growth models, there was greater support for the logistic and Gompertz models than the von Bertalanffy model, regardless of ageing error assumptions. The von Bertalanffy model, however, appeared to fit the data well enough to permit survival estimates; using length‐based estimators, annual survival varied between 0·64 (95% credibility interval: 0·44–0·79) and 0·81 (0·79–0·83) depending on ageing and growth process error structure. These estimates are applicable to conservation and management of L. richardsoni and other western lampreys (e.g. Pacific lamprey Entosphenus tridentatus) and can potentially be used in the development of life‐cycle models for these species. These results also suggest that estimators derived from von Bertalanffy growth models should be interpreted with caution if there is high uncertainty in age estimates.     

Population biology of the red gurnard (Aspitrigla cuculus L.; Triglidae) in the inshore waters of Eastern Anglesey and Northwest Wales

ICES has identified red gurnard Aspitrigla cuculus (L.) as a potential commercial species and recommended that monitoring programmes should be conducted to derive information on biological parameters for stock assessment purposes. In this paper, data on the population biology of red gurnard in the coastal waters of Northwest Wales and Eastern Anglesey are presented. Total length (TL) of fish sampled ranged from 15.4 to 35.0 cm (males) and 10.5 to 43.1 cm (females), with the majority of females between 20 and 30 cm TL (70.0%) and males between 20 and 30 cm TL (71.0%). TL/weight (W) relations were similar between immature and mature individuals for both sexes and between both sexes (all maturity stages combined), producing a combined data equation W = 0.005 TL^3.19. Age of fish ranged from 1 to 7 years and 1 to 6 years, respectively, for females and males, with the majority of females age 3 (37%) and the majority of males age 2 (49%). The age structures of female and male red gurnards were significantly different, with the older age classes consisting predominantly of female fish. Both males and females exhibited similar asymptotic growth patterns; the combined von Bertalanffy growth function was . Instantaneous rates of total mortality were calculated as 1.13 year^?1 for males and 0.98 year^?1 for females. The size (L₅₀) and age at first maturity (A₅₀) were estimated to be 26.3 cm TL and 3.6 years for males, 28.1 cm TL and 3.5 years for females and 25.6 cm TL and 3.7 years for both sexes combined.     

Age, growth, maturity, and mortality of the Alaska skate, Bathyraja parmifera, in the eastern Bering Sea

The Alaska skate, Bathyraja parmifera, is the most abundant species of skate on the eastern Bering Sea shelf, accounting for over 90% of total skate biomass. However, little is known regarding the life history of this species despite its common occurrence as bycatch in several Bering Sea fisheries. This is the first study to focus on the age and growth of B. parmifera. From 2003 to 2005, more than one thousand specimens were collected by fisheries observers and on scientific groundfish surveys. Annual banding patterns in more than 500 thin sections of vertebral centra were examined for age determination. Caudal thorns were tested as a potentially non-lethal ageing structure. Annual band pair deposition was verified through edge and marginal increment analyses. A three-parameter von Bertalanffy growth function and a Gompertz growth function were fit to observed length-at-age data. Both models provided significant fits, although the Gompertz function best described the overall pattern of growth in both males and females, based upon statistical criteria and parameter estimates. Age and size at 50% maturity were 9 years and 92 cm TL for males and 10 years and 93 cm TL for females. The maximum observed ages for males and females were 15 years and 17 years, respectively. Estimates of natural mortality (M) ranged from 0.14 to 0.28, and were based on published relationships between M and longevity, age at maturity, and the von Bertalanffy growth coefficient. Due to these life history characteristics and a lack of long-term species-specific stock data, a conservative management approach would be appropriate for B. parmifera.     

Spawning,maturity, growth and movement of Platycephalus fuscus (Cuvier, 1829) (Platycephalidae): fishery management considerations

The dusky flathead (Platycephalus fuscus) is an important teleost harvested by recreational and commercial fishers throughout its endemic distribution along eastern Australia. This study indicates that the species has an extended spawning period throughout the austral summer, with females in spawning condition occurring in lower estuarine and coastal waters. Total length (L₅₀) and age (A₅₀) at which 50% (±1 SE) of the population was mature was 31.72 (±1.08) cm TL and 1.22 (±0.44) years for males and 56.75 (±0.60) cm TL and 4.55 (±0.13) years for females. The von Bertalanffy growth parameters differed significantly between sexes; females grew faster and attained a greater maximum TL and age than males. The largest female was 98.5 cm TL (7.5 kg), and the oldest 16 years, whereas the largest male was 61.5 cm TL (1.58 kg) and 11 years of age. A tag‐and‐release study identified the exchange of sub‐adult and mature‐sized individuals among estuaries. Determinations of length‐based management regulations for the species are compounded by the large gender‐based differences in growth and length‐at‐maturity. Current minimum legal lengths of 30–40 cm TL protect approximately 3–9% of the female spawning population. Alternative management options, including harvest slot sizes, need to be investigated and tested.     

Growth and derived life-history characteristics of the Brazilian electric ray Narcine brasiliensis

The majority of batoids are listed as Threatened (20.4%) or Data Deficient (41%) by the IUCN Red List. A key challenge to assessing Data-Deficient species is obtaining estimates of key life-history characteristics. Here, a Bayesian approach was used to estimate derived life-history characteristics from a growth model applied to the Data-Deficient Brazilian electric ray Narcine brasiliensis. The age of 170 specimens (107 females, 63 males) was estimated from vertebral centra, and total length, disc width, total weight and birth size were used in a joint estimation of sex-specific length-weight models and two-dimensional von Bertalanffy growth models. Estimates of age at length zero, age at maturity, longevity and mortality at age were derived simultaneously. The Bayesian joint modelling approach was robust to small sample sizes by adding a likelihood to constrain L₀ and sharing parameters, such as Brody growth coefficient between length measurements. The median growth parameter estimates were a shared L₀ = 38.8 mm, female L_∞ = 515 mm, 𝑘 = 0.125 and male L_∞ = 387 mm, 𝑘 = 0.194. Age at maturity was estimated to be 7.40–7.49 years for females and 4.45–4.47 years for males, whereas longevity was 22.5–22.6 years for females and 14.2 years for males depending on length measurement. Age-1 natural mortality was estimated to be 0.199–0.207 for females and 0.211–0.213 for males. The derived life-history characteristics indicate N. brasiliensis is earlier maturing, but slower growing relative to other Torpediniformes. These characteristics along with the species’ endemism to southern Brazil and high by-catch rates indicate that one of the IUCN Red List threatened categories may be more appropriate for the currently Data-Deficient status. The Bayesian approach used for N. brasiliensis can prove useful for utilizing limited age-growth data in other Data-Deficient batoid species to inform necessary life characteristics for conservation and management.     

Evidence of sustained populations of a small reef fish on artificial structures. Does depth affect production on artificial reefs?

The length frequencies and age structures of resident Pseudanthias rubrizonatus (n = 407), a small protogynous serranid, were measured at four isolated artificial structures on the continental shelf of north-western Australia between June and August 2008, to determine whether these structures supported full (complete size and age-structured) populations of this species. The artificial structures were located in depths between 82 and 135 m, and growth rates of juveniles and adults, and body condition of adults, were compared among structures to determine the effect of depth on potential production. All life-history stages, including recently settled juveniles, females and terminal males, of P. rubrizonatus were caught, ranging in standard length (L(s)) from 16·9 to 96·5 mm. Presumed ages estimated from whole and sectioned otoliths ranged between 22 days and 5 years, and parameter ±s.e. estimates of the von Bertalanffy growth model were L(∞) = 152 ± 34 mm, k = 0·15(±0·05) and t(0) = -1·15(±0·15). Estimated annual growth rates were similar between shallow and deep artificial structures; however, otolith lengths and recent growth of juveniles differed among individual structures, irrespective of depth. The artificial structures therefore sustained full populations of P. rubrizonatus, from recently settled juveniles through to adults; however, confirmation of the maximum age attainable for the species is required from natural populations. Depth placement of artificial reefs may not affect the production of fish species with naturally wide depth ranges.     

Growth characteristics of freshwater pearl mussels,Margaritifera margaritifera (L.)

• 1 Shell growth in the freshwater pearl mussel, Margaritifera margaritifera, was investigated. Three non‐linear growth models (i.e. power, logistic and von Bertalanffy) were fitted to Scottish length‐at‐age data sets and compared.
• 2 Overall, the von Bertalanffy model outperformed the other two approaches, generating the smallest residuals in eight out of 11 samples (the logistic model provided slightly better fits to the other three). It was concluded that individual M. margaritifera appear to grow in an approximately asymptotic fashion and that the von Bertalanffy equation is an appropriate growth model to fit to freshwater pearl mussel length‐at‐age data.
• 3 The ranges in von Bertalanffy parameter estimates observed (k = 0.023–0.075 year^‐1, L_∞ = 77–158 mm, t_o = ‐3.93–4.33 years) are typical of those reported in northern European populations.
• 4 Most of the populations investigated had relatively low k‐values and high maximum age (A_max) estimates. This feature, which suggests high long‐term productivity and less vulnerability to decline (i.e. larger, longer‐living mussels produce more offspring), may be a reason why these populations have survived until now. The population which appears to be the most vulnerable (i.e. which has the highest k and lowest A_max) is probably not recruiting adequately at present.
• 5 An index of absolute growth (mean shell length‐at‐age) was also used for comparing different populations. Observed between‐ and within‐river differences in mussel growth patterns may be associated with a number of environmental factors, particularly water temperature and productivity.
• 6 A significant positive relationship between river length and mean mussel length‐at‐age was observed. In general, mussels grow large in large, cold rivers and vice versa, although there are exceptions which suggest that additional factors may be involved.