Age estimates derived from hard parts of swordfish Xiphias gladius from the north-western Mediterranean Sea

Accurate age estimates for fish are critical for properly understanding stock dynamics and health; this is particularly true for larger billfishes. Here we determined the most accurate aging estimation methods for swordfish (Xiphias gladius). We compared age estimates obtained from fin-ray sections, otolith sections, whole otoliths, and vertebrae collected from 87 swordfish off the east coast of Corsica. Age estimates from otolith sections were most consistently estimated across different readers (lowest average percentage error), followed by fin-ray sections, third vertebrae, and whole otoliths. When the age estimates from the otolith sections were compared with the other three age sclerochronological methods, we found the average percentage error to be lowest between the otolith section and fin-ray methods. However, age estimates from fin rays proved most useful for estimating swordfish younger than 6 years, as the fin ray-based age diverged from that of the otolith sections as the swordfish aged. Combining fin ray and otolith section techniques, we estimated the growth parameters of 1–12-year-old females (L_∞ = 259.412, k = 0.113, t₀ = −2.499) and 1–7-year-old males (L_∞ = 175.543, k = 0.202, t₀ = −2.239). We found that females grew significantly faster than males after 3 years and remained larger thereafter. Our calculated growth rates for this region of the north-western Mediterranean Sea were lower than those of the Atlantic, Pacific, and eastern Mediterranean Sea swordfish populations, and similar to growth rates recorded for the western Mediterranean Sea populations. Our study provides critical knowledge on biological-related parameters to serve as a guide for preserving the swordfish population in the Mediterranean Sea.     

Reproductive biology,growth, and age composition of non‐native Indian glassy fish Parambassis ranga (Hamilton, 1822) in Haebaru Reservoir,Okinawa‐jima Island,southern Japan

Age composition, growth, and reproductive biology of the non‐native Indian glassy fish Parambassis ranga (Hamilton, 1822) were surveyed in the Haebaru Reservoir on Okinawa‐jima Island, southern Japan. Standard lengths (SLs) of males and females ranged from 19.7 to 44.0 mm and from 19.2 to 52.4 mm, respectively. The overall sex ratio was significantly female‐biased, with the monthly percentage of females ranging from 71.4 to 100.0. Marginal growth analysis of sectioned otoliths revealed opaque zones formed annually from November to May. Observed age ranged from 0 to 3 years for both sexes, although the 1‐year age class comprised the majority of the sampled population. Von Bertalanffy growth parameters were L_∞ = 48.8 mm (SL), K = 0.43 year^?1, and t₀ = ?1.47 years for males, and L_∞ = 43.7 mm, K =0.72 year^?1, and t₀ = ?1.29 years for females. Length at 50% maturity was estimated to be 25.8 mm SL, and maturation was within 1 year after hatching. The main spawning season of P. ranga was estimated to occur from February to October, peaking in April.     

Validated age,growth and maturity of the bonnethead Sphyrna tiburo in the western North Atlantic Ocean

The age, growth and maturity of bonnetheads Sphyrna tiburo inhabiting the estuarine and coastal waters of the western North Atlantic Ocean (WNA) from Onslow Bay, North Carolina, south to West Palm Beach, Florida, were examined. Vertebrae were collected and aged from 329 females and 217 males ranging in size from 262 to 1043 mm and 245 to 825 mm fork length, L_F, respectively. Sex‐specific von Bertalanffy growth curves were fitted to length‐at‐age data. Female von Bertalanffy parameters were L_∞ = 1036 mm L_F, k = 0·18, t₀ = ?1·64 and L₀ = 272 mm L_F. Males reached a smaller theoretical asymptotic length and had a higher growth coefficient (L_∞ = 782 mm L_F, k = 0·29, t₀ = ?1·43 and L₀ = 266 mm L_F). Maximum observed age was 17·9 years for females and 16·0 years for males. Annual deposition of growth increments was verified by marginal increment analysis and validated for age classes 2·5+ to 10·5+ years through recapture of 13 oxytetracycline‐injected specimens at liberty in the wild for 1–4 years. Length (L_F50) and age (A₅₀) at 50% maturity were 819 mm and 6·7 years for females, and 618 mm and 3·9 years for males. Both female and male S. tiburo in the WNA had a significantly higher maximum observed age, L_F50, A₅₀ and L_∞, and a significantly lower k and estimated L₀ than evident in the Gulf of Mexico (GOM). These significant differences in life‐history parameters, as well as evidence from tagging and genetic studies, suggest that S. tiburo in the WNA and GOM should be considered separate stocks.     

Age and growth of Brauer's lanternfish Gymnoscopelus braueri and rhombic lanternfish Krefftichthys anderssoni (Family Myctophidae) in the Scotia Sea,Southern Ocean

This study examines age and growth of Brauer's lanternfish Gymnoscopelus braueri and rhombic lanternfish Krefftichthys anderssoni from the Scotia Sea in the Southern Ocean, through the analysis of annual growth increments deposited on sagittal otoliths. Otolith pairs from 177 G. braueri and 118 K. anderssoni were collected in different seasons from the region between 2004 and 2009. Otolith-edge analysis suggested a seasonal change in opaque and hyaline depositions, indicative of an annual growth pattern, although variation within the populations of both species was apparent. Age estimates varied from 1 to 6 years for G. braueri (40 to 139 mm standard length; L_S) and from 0 to 2 years for K. anderssoni (26 to 70 mm L_S). Length-at-age data were broadly consistent with population cohort parameters identified in concurrent length-frequency data from the region for both species. The estimated values of von Bertalanffy growth curves for G. braueri were L_∞ = 133.22 mm, k = 0.29 year⁻¹ and t₀ = −0.21 year and the values for K. anderssoni were L_∞ = 68.60 mm, k = 0.71 year⁻¹ and t₀ = −0.49 year. There were no significant (P > 0.05) differences in growth between sexes for either species, suggesting that males and females have similar growth and development trajectories in the Scotia Sea. A positive allometric relationship between L_S and wet mass was found for each species, as well as a significant (P < 0.0001) linear relationship between otolith size and L_S. Growth performance (Ф′) was similar between the two species and congruent with other myctophid species across the Southern Ocean. This study provides important parameters for future Southern Ocean ecosystem studies in a resource management context.     

Growth and length–weight relationships of Sander lucioperca (Linnaeus, 1758) in the Alcántara Reservoir,south‐western Spain: comparison with other water bodies in Eurasia

Growth parameters in pikeperch may be affected by several factors. The purpose of this study was to investigate the growth and length–weight of pikeperch in a reservoir in south‐western Spain and compare the results with previous published data. Age and growth are described for Sander lucioperca from the Alcántara Reservoir (south‐western Spain) from March to October 2009. A total of 285 fish were examined; the ratio of males to females was estimated as 0.78:1 and age ranges as 1–5 years. Total lengths ranged from 16.1 to 52.5 cm. The length–weight relationships were described as W = 0.00 462 TL^3.09 (r = 0.9865) for males and W = 0.00279 TL^3.16 (r = 0.9921) for females. Growth was expressed in length and the von Bertalanffy growth parameters were estimated as L∞ = 92.14 cm, k = 0.09, t₀ = ?1.05 for males and L∞ = 107.72 cm, k = 0.08, t₀ = ?1.16 for females. Growth performance indexes were also estimated as Φ’ = 2.88 for males and Φ’ = 2.96 for females. Differences in growth and length–weight relationships between sexes were not found.     

The growth ofOreochromis andersonii (Pisces: Cichlidae) from the Okavango Delta,Botswana, and a comparison of the scale and otolith methods of ageing

Synopsis Otoliths and scales were used for age and growth determination ofOreochromis andersonii from the Okavango Delta, Botswana. Marginal increment analysis showed that an annulus was formed in both the scales and otoliths during the dry summer period. Using scales, the growth ofO. andersonii was described by L_t = 285.27(1-e^{-0.26(t+2.02)}) mm SL and using otoliths by the equation L_t = 267.48(1-e^{-0.25(t+2.18)}) mm SL. Maximum age estimates of 10 years using scales and 13 years using otoliths were obtained and the growth curves were significantly different (p < 0.01). Age estimation using scales tended to over-emphasise growth inO. andersonii resulting in larger predicted lengths-at-age. For this reason, otoliths are considered to be more reliable and suitable than scales in determining the age and growth of this species.     

Age,growth and maturity of the pelagic thresher Alopias pelagicus and the scalloped hammerhead Sphyrna lewini

Indonesia has the greatest reported chondrichthyan catches worldwide, with c.110,000 t caught annually. The pelagic thresher (Alopias pelagicus) and scalloped hammerhead (Sphryna lewini) together comprise about 25% of the total catches of sharks landed in Indonesia. Age and growth parameters were estimated for A. pelagicus and S. lewini from growth‐band counts of thin‐cut vertebral sections. Alopias pelagicus (n = 158) and S. lewini (n = 157) vertebrae were collected from three Indonesian fish markets over a 5 year period. A multi‐model analysis was used to estimate growth parameters for both species. The models of best fit for males and females for A. pelagicus was the three‐parameter logistic (L_∞ = 3169 mm L_T, k = 0·2) and the two‐parameter von Bertalanffy models (L_∞ = 3281 mm L_T, k = 0·12). Age at maturity was calculated to be 10·4 and 13·2 years for males and females, respectively, and these are the oldest estimated for this species. The samples of S. lewini were heavily biased towards females, and the model of best fit for males and females was the three‐parameter Gompertz (L_∞ = 2598 mm L_T, k = 0·15) and the two‐parameter Gompertz (L_∞ = 2896 mm L_T, k= 0·16). Age at maturity was calculated to be 8·9 and 13·2 years for males and females, respectively. Although numerous age and growth studies have previously been undertaken on S. lewini, few studies have been able to obtain adequate samples from all components of the population because adult females, adult males and juveniles often reside in different areas. For the first time, sex bias in this study was towards sexually mature females, which are commonly lacking in previous biological studies on S. lewini. Additionally, some of the oldest aged specimens and highest age at maturity for both species were observed in this study. Both species exhibit slow rates of growth and late age at maturity, highlighting the need for a re‐assessment of the relative resilience of these two globally threatened sharks at current high levels of fishing mortality throughout the eastern Indian Ocean.     

Age and growth of the Black Sea turbot, Psetta maxima (Linneaus, 1758) (Pisces: Scophthalmidae), estimated by reading otoliths and by back-calculation

Age and growth of the Black Sea turbot, Psetta maxima, were determined from a total of 1445 individuals collected along the eastern Black Sea coast between 1990 and 1996. Age was estimated by interpreting growth rings in whole and broken sagittal otoliths. The former method underestimated the age over 5 years, and a maximum age of 11 years was observed by the latter. Marginal increment analysis clearly showed that a single annulus is formed in early summer each year. Growth in length differed between sexes, and females attained a larger size than males at the same age. No significant difference was found between the mean observed total length (TL), the back‐calculated TL derived from radius measurements and the TL estimated from otolith size–fish size relationship. The von Bertalanffy growth parameters estimated by the length‐at‐age data were: L_∞ = 96.24 cm; K = 0.119 year^?1; t₀ = ?0.01 year for the entire population.     

Age,growth and mortality of common two‐banded seabream,Diplodus vulgaris (Geoffroy Saint‐Hilaire, 1817), in the eastern Adriatic Sea (Croatian coast)

Age, growth and mortality were analysed for the common two‐banded seabream, Diplodus vulgaris, collected in the eastern Adriatic (Croatian coast) from commercial fishery catches by ‘tramata’ fishing (2005–2006) to obtain growth estimation. The oldest female was estimated to be age 11, the oldest male age 10 years. The von Bertalanffy growth parameters estimated by reading scales were: L_∞ = 48.60 cm (SE = 1.101), K = 0.112 (SE = 0.005) and t₀ = ?2.366 (SE = 0.060) for all specimens; L_∞ = 51.96 cm (SE = 2.153), K = 0.095 (SE = 0.007) and t₀ = ?2.837 (SE = 0.120) for females and L_∞ = 56.25 cm (SE = 2.662), K = 0.084 (SE = 0.067) and t₀ = ?2.920 (SE = 0.117) for males. The overall sex ratio was 1.22 : 1 in favour of males. Total mortality, corresponding to the slope of the descending limb of the catch curve, was Z = 0.81 per year for females and Z = 0.85 per year for males. Exploitation ratios were E = 0.68 for females and E = 0.73 for males.     

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,growth, and age at sexual maturity of the commercially landed skate species,Dipturus chinensis (Basilewsky, 1855), in the northern East China Sea

Age, growth, and age at sexual maturity of the polkadot skate Dipturus chinensis, in the northern East China Sea were determined for a total of 614 specimens collected from April 2009 to December 2014. Vertebral centrum analysis was used to calculate the age of the skates. Annual band deposition was determined by marginal increment analysis. The von Bertalanffy growth model was fitted to the observed length‐at‐age data for each sex (males, L_∞ = 76.8, k = 0.109, t₀ = ?1.28; females, L_∞ = 83.1, k = 0.103, t₀ = ?1.20). Growth patterns of females and males were similar until the age of 6; thereafter, females grew larger than males. Maximum age recorded was 13 years for males and 15 years for females. Age at 50% sexual maturity was 8.22 years for males and 9.39 years for females. These results indicate that D. chinensis is slow growing, relatively long‐lived, and late maturing, and therefore vulnerable to exploitation.     

Age,growth and mortality of Lutjanus alexandrei in estuarine and coastal waters of the tropical south‐western Atlantic

Otolith‐based methods were used to determine life history traits of the endemic Brazilian snapper (Lutjanus alexandrei) in estuarine and coastal environments in the south‐western Atlantic. Fishes were caught as juveniles inside mangrove‐bordered estuaries by traditional corral fisheries whereas adults were captured at sea using motorboats with trap and gill nets. Fish were sampled during landings and 331 otolith pairs were extracted from L. alexandrei. Inshore mangroves comprised individuals of 0–4 years (mean: 2 years), while individuals in deeper reef environments were older (range: 3–22; mean: 8 years), indicating an ontogenetic shift at approximately age 3 or 4. Edge analysis was used to validate the annual deposition in the otoliths, suggesting that opaque growth rings were formed between April and September. Age‐at‐length data were used to predict L. alexandrei growth rates using the von Bertalanffy growth model from where the parameters were calculated: L_∞ = 31 cm, k = 0.24, t₀ = ?1.26, r² = 0.97. Mortality rates were estimated for coastal habitats, with Z = 0.22 and S = 0.78 year^?1, based on ages 7–17. Additionally, evidence of ontogenetic migration is provided by age and size structure.     

Age and growth of Schizopygopsis younghusbandi younghusbandi in the Yarlung Zangbo River in Tibet, China

Schizopygopsis younghusbandi younghusbandi is an endemic species whose distribution is restricted to the middle reaches of the Yarlung Zangbo River, being one of the most important commercial fishes in this area. Age and growth of 606 specimens captured between October 2002 and April 2005 were studied. The range in standard length (L) was 65.7–387.3 mm and total weight (W) was 3.3–772.0 g. The relationship between L and W was W = 0.000909L^2.2493 for males and W = 0.000259L^2.4781 for females. Age, determined from anal scales and lapillus otoliths, ranged from 3 to 18 years. The parameters of von Bertalanffy growth functions, estimated by back-calculated length, were L_￥ = 442.7mm  LL_\infty = 442.7mm\;L, k = 0.0738 year⁻¹ and t ₀  = −1.4 year for males, and L_￥ = 471.4mm  LL_\infty = 471.4mm\;L, k = 0.0789 year⁻¹ and t ₀ = 0.2 year for females. Males and females exhibited statistically significant differences in growth. χ ²-test indicated that von Bertalanffy growth functions could well describe the growth of S. y. younghusbandi. The longevities were 39.2 and 38.2 years for males and females, respectively. Growth inflexion points were 10.2 and 12.0 years for males and females, respectively, but 84.8% of the captures were at the smaller ages. So conservation and management schemes for this population should be considered urgently. In addition, we found that populations from the upstream of the Lhasa River, the downstream of the Lhasa River and the middle reaches of the Yarlung Zangbo River showed statistically significant differences in growth patterns.     

Age and growth of the gulf toadfish Opsanus beta based on otolith increment analysis

In the present study, sagittal otoliths of confirmed male and female specimens of the gulf toadfish Opsanus beta that were collected monthly over the course of a year from Biscayne Bay, Florida, U.S.A. were analysed. The timing and frequency of O. beta spawning seasons are reported by examination of the gonado‐somatic index. The estimated ages of males and females ranged from < 1 year to 6 and 5 years, respectively. Strong sexual dimorphism in growth was apparent with von Bertalanffy parameter estimates for males of L_∞ = 393·8 mm, K = 0·30, t₀ = 0·36 and females of L_∞ = 201·1 mm, K = 0·79, t₀ = 0·47. Comparison with previously published growth trajectories of the more northerly distributed conspecific Opsanus tau showed that O. beta males had a higher growth rate. Female O. beta and O. tau growth trajectories appear similar, with an indication that the former becomes asymptotic at least a year before the latter. Results are discussed in the context of temperature regimes, reproductive energy allocation and waste urea excretion in the two species.     

Population biology and assessment of the white-spotted spinefoot, Siganus canaliculatus (Park, 1797), in the southern Arabian Gulf

The age, growth, mortality, reproduction and resource status of Siganus canaliculatus in the southern Arabian Gulf were investigated using a combination of size frequency, biological and size‐at‐age data. Defined structural increments consisting of alternating translucent and opaque bands in transverse sections of sagittal otoliths were validated as annuli. The maximum absolute age estimate was 7.8 years. Parameter values of the von Bertalanffy growth function fit to size‐at‐age data (males and females combined) were: k = 1.0, L_∞ = 24.8 cm (L_F), t_o = −0.1 years. Fish in spawning condition were only observed between April and July although patterns in gonadosomatic indices suggested a second but less well defined spawning event in November. The mean sizes and ages at first sexual maturity were 21.5 cm L_F (1.9 years) for males and 25.7 cm L_F (2.1 years) for females. Fish were fully recruited to the fishery at a size (L₁₀₀ = 19.7 cm L_F) that was smaller than the sizes at which sexual maturity was attained. The annual instantaneous rate of fishing mortality (F = 0.85 year⁻¹) (0.26–1.44 year⁻¹ 95% CI) was considerably greater than the target (F_opt = 0.33 year⁻¹) and limit (F_limit = 0.44 year⁻¹) biological reference points, indicating that the stock is overexploited.     

Age,growth, and reproductive biology of blacktail snapper,Lutjanus fulvus,around the Yaeyama Islands,Okinawa, Japan

Age, growth, and reproductive characteristics of blacktail snapper, Lutjanus fulvus, which is a commercial fish species, were investigated using 322 specimens (40–332 mm in fork length) caught around the Yaeyama Islands, Okinawa, Japan. Spawning season was estimated to be from April to October, and spawning was confirmed around the full moon and the last quarter moon. Age determination using sectioned otoliths revealed that ages ranged from 0 to 34 years and the majority was ≥ 3 years. Parameters of the von Bertalanffy growth function were estimated to be L _∞  = 270 mm, k = 0.40, and t ₀  = ?0.48 years for females, and 257 mm, 0.44, and ?0.42 years for males. Initial growth was rapid during the first 3 years, attaining over 200 mm for both sexes, and then females grew larger than males. Sizes (ages) at the first sexual maturity were 225 mm (4 years) for females and 207 mm (3 years) for males. The wide range of age composition in catch with majority of ≥3 years old implied that the current fishing effort to harvest was not sufficiently large enough to collapse the stock immediately.     

Age and growth of the hollowsnout grenadier, Caelorinchus caelorhincus (Risso, 1810), in the Aegean Sea

Age and growth of the hollowsnout grenadier was studied based on samples collected seasonally in the Agean Sea between March 2003 and January 2004. Total length ranged from 9.0 to 21.6 cm. Length–weight relationship was described as a = 0.0032, and b = 3.008. Age determinations based on otolith readings were between 1 and 10 years. The von Bertalanffy growth curve fitted to observed lengths‐at‐age provided parameters of L_∞ = 24.9 cm, k = 0.115 and t_o = ?3.494.     

Growth and reproduction of Chelidonichthys lucerna (Linnaeus) (Pisces: Triglidae) in the Gulf of Gabès,Tunisia

Growth and reproduction of Chelidonichthys lucerna is reported from Tunisian waters. A total of 286 specimens was collected from landings of bottom trawlers between January 2003 and November 2004. The total length ranged from 16 to 36 cm in females and from 17 to 26 cm in males. Marginal increment analysis of otoliths showed that the translucent zone was laid from October to May and the opaque zone laid from June to September. Females were from 0.5 to 9 years and males from 1 to 7 years old. Growth parameters of the von Bertalanffy growth function were TL_∞ = 40.26; K = 0.06 and t₀ = ?3.03 in females and TL_∞ = 46.16; K = 0.059 and t₀ = ?1.32 in males. The coefficient of the allometric length–weight relationships differed significantly by sex. Females with mature gonads were observed between October and May, with peaks in January and February. Length at which 50% of specimens were mature was 21.6 cm TL (estimated age about 3 years) in females and 19.2 cm TL (estimated age about 1.5 years) in males.     

Reproduction,growth and feeding habits of stout beardfish Polymixia nobilis (Polymixiidae) off the Canary Islands (NE Atlantic)

The present study provides fisheries biology knowledge which will allow the implementation of regulatory measures contributing to the sustainability of the fisheries and the conservation of the stout beardfish Polymixia nobilis Lowe, 1838 off the Canary Islands, north eastern Atlantic Ocean. Males ranged between 16.5 and 38.4 cm fork length (FL) and females from 14.2 to 46.5 cm FL. Sex ratio by size classes provided significant differences in classes higher than 36 cm, being clearly unbalanced in favour of females. Individuals in maturing and mature stages were present during all months sampled, although a spawning peak is evident between April and June. Size at first maturity was estimated as 26 cm FL for females and 30 cm FL for males. Age was determined from annuli in whole otoliths. Age range was found to be 0–14 years for fish measuring 14.2 to 46.5 cm FL. It is a slow‐growing and long‐lived species. Significant differences in the growth parameters between sexes were detected. The von Bertalanffy growth parameters estimated for females (n = 213) were L_∞ = 45.92 cm LF, k = 0.16 years^?1 and t₀ = ?2.84 years; and for males (n = 186) L_∞ = 36.44 cm LF, k = 0.26 years^?1 and t₀ = ?2.16 years. Stomach analysis indicated some variations in the feeding habits with growth: individuals of small and medium sizes preyed on crustaceans and fishes, while large specimens preyed mainly on fishes.     

Age and growth in pink cusk-eel (Genypterus blacodes) off the Chilean austral zone: evaluating differences between management fishing zones

The von Bertalanffy (vB) growth parameters for pink cusk‐eel (Genypterus blacodes) were estimated for the Chilean austral‐zone (41°28′–57°00′S) by gender and management fishing zones. A total of 47 026 samples were collected between March 1982 and May 2004, with total length ranging from 19 to 154 cm. Age determinations, based on the reading of saggital otoliths, were between 1 and 14 years in males and between 1 and 16 years in females. Statistical differences in growth were found between the sexes and management fishing zones. For the combined sexes the vB growth parameters for the northern‐austral zone (41°28′–47°00′S) were: l_∞=111.452 cm, k = 0.186 year⁻¹, t₀ = −0.912 year; and for the southern‐austral zone (47°00′–57°00′S): l_∞ = 123.447 cm, k = 0.147 year⁻¹, t₀ = −1.779 year.