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.     

Distribution and population structure of the Chlorophthalmus agassizi (Bonaparte, 1840) on an unexploited fishing ground in the Greek Ionian Sea

The distribution and population structure of the shortnose green eye, Chlorophthalmus agassizi, were studied in the Greek Ionian Sea using data collected during experimental trawl surveys carried out from December 1996 to November 1997. The length–frequency distribution ranged between 45 and 201 mm total length (TL). The significant increase in average size linked with depth has been observed, supporting the general ‘bigger‐deeper’ phenomenon. Specifically, 1528 individuals were measured in the 300–400 m depth zone with a mean TL = 101 mm, 2351 individuals in the 400–500 m depth zone with a mean TL = 132 mm and 1889 individuals in the 500–600 depth zone with a mean TL = 145 mm. Age and growth of the population were determined by otolith readings. Twelve age groups were identified. The von Bertalanffy growth function (VBGF) parameters were L_∞=202.22 mm, K=0.20 and t_o=?1.6 years. Natural mortality was estimated at 0.285 per year, while total mortality was estimated at 0.65. The reproductive period of C. agassizi extends from spring to autumn, with greater activity in the summer.     

Fluctuating asymmetry and fitness correlations in two Engraulis encrasicolus populations

Correlations among several measures of fluctuating asymmetry (FA) and fitness‐related variables were assessed in two populations of the European anchovy Engraulis encrasicolus with fast growth (Aegean Sea) and slow growth (Ionian Sea), respectively. FA levels were borderline significantly higher in the Ionian than in the Aegean for some variables. Variation in otolith shape (deviation from population norm) was lower in the Ionian than the Aegean, contrary to expectation. Within the Aegean, there was no relation between any of the FA indexes and fitness estimators, while in the Ionian a composite otolith FA index was significantly negatively correlated to standard length at age only in 2 year‐old individuals. This difference between the Aegean and Ionian may have been related to the lower growth rate in the Ionian, as FA–fitness relations may be more apparent in less‐beneficial environments. The absence of significant correlations in the Aegean and the low correlation in one age group in the Ionian suggests that FA is not a sensitive indicator of individual fitness in adult E. encrasicolus.     

Population structure and growth of the Japanese littleneck clam <Emphasis Type="Italic">Ruditapes philippinarum</Emphasis> in Amursky Bay,Sea of Japan

This paper deals with the size, age, and sex structure of population and growth of the Japanese littleneck clam Ruditapes philippinarum in Amursky Bay (Peter the Great Bay, Sea of Japan). One-year-olds and individuals with a shell length less than 19.8 mm were not found in the population under study. The population consisted mostly of 3-4-year-old clams (72.4%) with a shell length of 35–45 mm (67.8%). The maximum recorded age of R. philippinarum was 7 years, and maximum shell length was 52.7 mm. The male to female ratio was approximately 2: 1. Hermaphroditism (2.1%) and parasitic castration (1.4%) were observed. Linear growth rates of clams were found to increase until the age of three years old (11.6 ± 0.6 mm/year). Mollusks reach a commercial size of over 35 mm in shell length in the fourth year of life. The parameters of the von Bertalanffy equation describing group linear growth were L _∞ = 56.6 mm, k = 0.302 year^?1, and t ₀ = 0.468 year. The relationship between the shell length and the wet body weight is described by the equation W = 0.000253L^2.954.     

The relationship between somatic growth and otolith dimensions of Mediterranean horse mackerel (Trachurus mediterraneus) from the Black Sea

In this study the relationships between somatic growth and otolith dimensions of Mediterranean horse mackerel (Trachurus mediterraneus) were investigated from samples obtained in the southeastern Black Sea area. It was concluded that there is a significant relationship between fish size and otolith dimensions. Therefore, age of Mediterranean horse mackerel can be estimated from otolith length and weight with sufficient certainty. This research was the first study of these relationships for T. mediterraneus from the Black Sea.     

Age estimation of juvenile European hake Merluccius merluccius based on otolith microstructure analysis: a slow or fast growth pattern?

The main goal of this study was to examine otolith microstructure and to estimate the age and growth of European hake Merluccius merluccius from the eastern Mediterranean Sea. One hundred and twenty‐nine specimens ranging from 102 to 438 mm in total length (L_T) were used. Age estimations were based on the study of the otolith microstructure, which was revealed after grinding both frontal sides of otoliths. The enumerations of the daily growth increments (DGI) as well as their width (W_DGI) measurements were made on calibrated digital images. The number of DGI in otoliths ranged between 163 and 717. Four phases in the W_DGI evolution were distinguished: (1) larval–juvenile pelagic phase, with an increasing trend in W_DGI up to the 60th DGI, (2) settlement phase, with a short‐term deceleration in W_DGI between the 61st and 150th DGI, (3) juvenile demersal phase, characterized by a stabilization of W_DGI from 151st to 400th DGI and (4) adult phase, with a decreasing trend in W_DGI after the 400th DGI. Age, sex and month of formation were found to affect the W_DGI in all phases, with the exception of age at the juvenile demersal phase. The power curve with intercept model described best the relationship of M. merluccius L_T with age (T_DGI), according to Akaike criteria, revealing differences in growth between females [L_T = 65 · 36(T_DGI)^{0 · 40} ? 388 · 55] and males [L_T = 69 · 32(T_DGI)^{0 · 37} ? 352 · 88] for the sizes examined. The mean daily growth rates were 0·61 mm day^?1 for females and 0·52 mm day^?1 for males, resulting in an L_T of 283 and 265 mm at the end of their first year of life. In comparison with previous studies on the Mediterranean Sea, the results of this study showed a greater growth rate, similar to results from tagging experiments and otolith microstructure analyses for M. merluccius in other geographic areas.     

Age and growth validation of the small spotted grunt Pomadasys commersonnii (Lacepède, 1801) from the northwestern coast of the Arabian Sea of Oman

Age structure and growth parameters were determined for a population of small spotted grunt, Pomadasys commersonnii in the Arabian Sea. Small spotted grunt samples were collected monthly between September 2007 and August 2008 by beam trawl [40 mm cod‐end mesh size] surveys conducted along the Arabian Sea coast of Oman from Ras Al‐Had in the north to the Oman‐Yemen border in the south west of Salalah between latitudes 16^o 33′N and 22^o 21′N and longitude 53^o 09′ and 59^o 55′ E and from depths of 20 to 250 m respectively. Marginal increment analysis of the sagittal otolith confirmed the deposition of annual increments on transverse sections, validating this technique for age and growth studies. Fish size (Fork Length, FL) ranged between 33–78 cm and age of fish ranged between 2 and 14 years with 5–9 years old fish comprising the majority of the catch. Both males and female exhibited asymptotic patterns of growth and the combined growth curve for both sexes provided von Bertalanffy growth (VBG) parameters of L_∞ = 77.2 cm FL (≡83.8 cm Total Length), k = 0.232/y and t₀ = ?0.058 y. VBG parameters, derived from Length‐Frequency Distribution Analysis (LFA) using ELEFAN1, PROJMAT and SLCA, obtained similar values (average values for the 3 methods: L_∞ = 78.8 cm FL, k = 0.35/y and t₀ = ?0.64 y) to those obtained from otolith analysis. A strong linear relationship was observed between otolith weight and age, and although age residuals ±4 years was observed between sagittal otolith age and estimated age (depending on sex and otolith weight), the results indicated that otolith weight could be used as a rapid proxy to estimate age and derive VBG parameters. In conclusion, both otolith ageing and LFA methods provided similar L_∞ and k values and the average values derived from all 4 methods lies within the auximetric plot for the species providing confidence in the VBG parameters obtained for small spotted grunt in the Arabian Sea.     

Life history characteristics and age validation of southern kingfish (Menticirrhus americanus (Linnaeus, 1758)) in the middle South Atlantic Bight

The purpose of this study was to determine critical components of the life history including otolith age validation, growth estimation, and reproductive characteristics for southern kingfish Menticirrhus americanus. A total of 2233 southern kingfish were collected from March 2009 to December 2010. Ages were estimated and validated using thin‐sectioned otoliths. Marginal increment analysis showed a single annulus was deposited once a year between April and May. Growth was significantly different (P < 0.0001) between sexes L_inf = 418.97 ± 16.58 mm, k = 0.29 ± 0.03, t₀ = ?1.30 ± 0.10 for females and L_inf = 290.74 ± 6.93 mm, k = 0.52 ± 0.05, t₀ = ?1.08 ± 0.11 for males. Southern kingfish spawn from March to August with a peak spawn in April. Based on evidence of multiple oocyte maturation stages and post‐ovulatory follicles (POFs) southern kingfish are multiple spawners exhibiting indeterminate fecundity. Spawning frequency for females ranging from 222 to 351 mm TL (age 1–5) was estimated as one spawning event every 2.0–4.2 days with up to 6 million total ova produced per spawning season per female.     

The distribution,size, and age composition,and growth of Saxidomus purpurata (Sowerby, 1852) (Bivalvia: Veneridae) in Vostok Bay,the Sea of Japan

Patterns of the distribution, the size and age composition of local populations, as well as the growth of the large bivalve Saxidomus purpurata, which is intensely farmed and reared in a number of East Asian countries, were studied for the first time in Russian Far East waters. It was determined that in the Vostok Bay, which is a bay of the second order within the limits of the Peter the Great Bay, S. purpurata forms local populations with densities of up to 7.5 ± 2.7 ind./m² and a biomass up to 1070.0 ± 384.0 g/m² at a depth of 1–9 m on mixed bottom substrates of boulders, pebbles, gravel, coquina, and sand of varying degrees of silting. The size and age composition of clam populations varies depending on the local environment; the shell length of the largest specimen was 98.6 mm, the greatest age was 23 years. In the Vostok Bay, the bivalve grew more slowly than off the coast of Korea and China and reached a commercial size (a shell length of 50 mm) later, at an age of 5–7 years. The von Bertalanffy equation describing the growth of S. purpurata in the aggregate sample of individuals from the Vostok Bay, has the form: L _t = 100.1[1 ? e^{?0.1675(t ? 0.0504)}]. It is assumed that the boundary of the species range goes north from the Peter the Great Bay, Sea of Japan.     

Age and growth of early-life-stage Atlantic tarpon (Megalops atlanticus) from the northcentral Gulf of Mexico

Age and growth of early-life-stage Atlantic tarpon Megalops atlanticus collected from Mississippi coastal waters in the northcentral Gulf of Mexico (GOM) are described using otolith microstructure analysis. Tarpon leptocephali (n = 95, 16.0—27.8 mm standard length, L_S) collected from June throughOctober 2013—2018, ranged in age from 22 to 43 days (mean = 30.9 ± 0.5 days). Leptocephalus somatic growth rates ranged 0.46—1.24 mm day⁻¹ (mean = 0.76 ± 0.02 mm day⁻¹), and leptocephalus otolith growth rates ranged 1.78—3.97 μm day⁻¹ (mean = 2.58 ± 0.04 μm day⁻¹). Growth rates were inversely correlated to leptocephalus age, indicating the shrinkage phase associated with leptocephalus metamorphosis. Juvenile tarpon (n = 358, 50—359 mm fork length, L_F) were collected from August through December 2007—2018. Juveniles exhibited a positive allometric relationship (adjusted R² = 0.99, P < 0.001) between length and mass. The age of 100 juveniles (71—277 mm L_F) ranged from 76 to 174 days. Juvenile growth rate was estimated as 1.56 ± 0.11 mm day⁻¹. Significant (P < 0.001) linear relationships were found between juvenile age and otolith metrics, including otolith mass (R² = 0.81) and radius (R² = 0.68). Evaluation of the backcalculated hatch dates suggests that specimens in the collection hatched from late May through mid-September with slight peaks during July and August. A Rao's Spacing Test of Uniformity indicates the presence of significant lunar periodicity in leptocephalus hatch dates (n = 95, U = 250.1, P < 0.05), with 50% of the leptocephali hatched within 5 days (before or after) of the full moon. This study fills critical gaps in the scientific knowledge of tarpon and provides estimates of early-life-history metrics for an iconic game fish at the northernmost extent of its GOM range.     

Into the depth of population genetics: pattern of structuring in mesophotic red coral populations

Deep-sea reef-building corals are among the most conspicuous invertebrates inhabiting the hard-bottom habitats worldwide and are particularly susceptible to human threats. The precious red coral (Corallium rubrum, L. 1758) has a wide bathymetric distribution, from shallow up to 800 m depth, and represents a key species in the Mediterranean mesophotic reefs. Several studies have investigated genetic variability in shallow-water red coral populations, while geographic patterns in mesophotic habitats are largely unknown. This study investigated genetic variability of C. rubrum populations dwelling between 55 and 120 m depth, from the Ligurian to the Ionian Sea along about 1500 km of coastline. A total of 18 deep rocky banks were sampled. Colonies were analyzed by means of a set of microsatellite loci and the putative control region of the mitochondrial DNA. Collected data were compared with previous studies. Both types of molecular markers showed high genetic similarity between populations within the northern (Ligurian Sea and Tuscan Archipelago) and the southern (Tyrrhenian and Ionian seas) study areas. Variability in habitat features between the sampling sites did not affect the genetic variability of the populations. Conversely, the patchy distribution of suitable habitats affected populations’ connectivity within and among deep coral banks. Based on these results and due to the emphasis on red coral protection in the Mediterranean Sea by international institutions, red coral could be promoted as a ‘focal species’ to develop management plans for the conservation of deep coralligenous reefs, a reservoir of marine biodiversity.     

Microsatellite and mitochondrial DNA analyses of Atlantic bluefin tuna (Thunnus thynnus thynnus) population structure in the Mediterranean Sea

Genetic variation was surveyed at nine microsatellite loci and the mitochondrial control region (868 bp) to test for the presence of genetic stock structure in young-of-the-year Atlantic bluefin tuna (Thunnus thynnus thynnus) from the Mediterranean Sea. Bluefin tuna were sampled over a period of 5 years from the Balearic and Tyrrhenian seas in the western basin of the Mediterranean Sea, and from the southern Ionian Sea in the eastern basin of the Mediterranean Sea. Analyses of multilocus microsatellite genotypes and mitochondrial control region sequences revealed no significant heterogeneity among collections taken from the same location in different years; however, significant spatial genetic heterogeneity was observed across all samples for both microsatellite markers and mitochondrial control region sequences (FST=0.0023, P=0.038 and PhiST=0.0233, P=0.000, respectively). Significant genetic differentiation between the Tyrrhenian and Ionian collections was found for both microsatellite and mitochondrial markers (FST=0.0087, P=0.015 and PhiST=0.0367, P=0.030, respectively). These results suggest the possibility of a genetically discrete population in the eastern basin of the Mediterranean Sea.     

Relationships between otolith size and fish length in some mesopelagic teleosts (Myctophidae,Paralepididae, Phosichthyidae and Stomiidae)

Length–mass relationships and linear regressions are given for otolith size (length and height) and standard length (L_S) of certain mesopelagic fishes (Myctophidae, Paralepididae, Phosichthyidae and Stomiidae) living in the central Mediterranean Sea. The length–mass relationship showed isometric growth in six species, whereas linear regressions of L_S and otolith size fit the data well for all species. These equations represent a useful tool for dietary studies on Mediterranean marine predators.     

Age validation and seasonal growth patterns of a subtropical marsh fish: The Gulf Killifish, <Emphasis Type="Italic">Fundulus grandis</Emphasis>

Fundulus grandis (Baird and Girard), the Gulf Killifish, is an abundant species throughout the marshes of the northern Gulf of Mexico. Its wide distribution and high site fidelity makes it an ideal indicator species for brackish and salt marshes, which experience a variety of anthropogenic disturbances. Despite the ecological, commercial, and scientific importance of F. grandis, age determination methods have not been validated and little is known of its growth pattern. By combining a tag-recapture study with a chemical marker to stain otoliths, we validated an ageing method for F. grandis adults (49–128 mm TL) using whole sagittal otoliths and determined growth rates of recaptured individuals in winter (n = 58) and summer (n = 36) in Louisiana. Mean somatic growth in length was significantly greater during the winter (0.085 mm d^?1) than summer (0.054 mm d^?1). In contrast, mean otolith growth was significantly greater in summer (1.37 μm d^?1) than winter (0.826 μm d^?1). The uncoupling of somatic and otolith growth may be primarily attributed to warm summer temperatures, which led to enhanced otolith growth while simultaneously reducing somatic growth. Fundulus grandis was aged to a maximum of 2.25 years. The parameters of the von Bertalanffy growth model were estimated as: L _∞  = 87.27 mm, k = 2.43 year^?1, and t ₀ = ?0.022. These findings reveal essential age and growth information for F. grandis and provide a benchmark to evaluate responses to environmental disturbances.     

Temporal variations in growth and reproduction of Tedania anhelans and Chondrosia reniformis in the North Adriatic Sea

Most works concerning growth and reproduction of Mediterranean sponges have been performed in the oligotrophic western Mediterranean while little is known about sponge dynamics in the North-western Adriatic Sea, a basin characterized by low winter temperature and eutrophy. In order to deepen our understanding of sponges in the North Adriatic Sea and verify how its peculiar trophic and physical conditions affect sponge life cycles, temporal trend of sponge cover (%) and reproductive timing of Chondrosia reniformis and Tedania (Tedania) anhelans were studied over a 1-year period looking for a possible relation with variations of temperature or food availability. In C. reniformis, although little variations of sponge cover were evidenced around the year, the number of individuals and their size increase during spring. Asexual reproduction, via drop-like propagules, mainly occurs in spring and summer, while sexual reproduction is characterized by a maximum number of oocytes in August. T. anhelans progressively grows from spring to summer and develops propagules on its surface that reach their maximum size in July. In autumn, the sponge undergoes a process of progressive shrinkage and almost disappears in winter when temperature reaches 7–8°C. Larvae occur during summer. In the North Adriatic Sea sponges have larger sizes, higher density and a wider period of oocytes production compared with the same species from the Mediterranean Sea, suggesting these differences could be due to high food availability characterizing the eutrophic Adriatic basin. On the contrary, the sharp water temperature variations and the very low winter temperature, 5–6°C lower than what has been reported for the Mediterranean Sea, regulate temporal variations in abundance and cause the disappearance of thermophile species during winter.     

The distribution, size and age compositions, and growth of the scallop Mizuhopecten yessoensis (Bivalvia: Pectinidae) in the northwestern Tatar Strait

The distribution patterns, size, age structure, and growth of the scallop Mizuhopecten yessoensis were studied in the northwest of the Tatar Strait, Sea of Japan. We determined that the northern boundary of the species range occurred in the region of Tabo Bay, at 51°37?? N. The distribution of the mollusk, depending on latitude, depth, substrate, and age, was determined. The maximum depth of M. yessoensis habitat is 138 meters, the maximum shell height is 200 mm, and the maximum age is 14 years. The differences in the growth rate of the Japanese scallop in different areas are discussed in relation to the conditions of its habitat in the northern part of its range.     

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.     

The life history of rock gurnard (Trigloporus lastoviza, Brünn. 1768) in the Saronikos Gulf

Age, growth and reproduction of rock gurnard in the Saronikos Gulf (Greece) were studied. Otoliths from 638 specimens (sex combined) were read for age determination. The body length-otolith radius relationship was found linear (L = -18.0 + 4.99 _xR; where L = fish length in mm, R = otolith radius 20 X). The life span of females seemed to be longer than that of males, indicating a differential mortality with sex. The growth was lower than that in the Catalane Sea. The maximum age of fish collected was VIII and the maximum fork length estimated by von Bertalanffy equation was 356 mm. Weight increased as the 3.054252 power or the length. Reproduction was observed to take place between winter and early spring and occasionally in early winter. Males began to mature after completion of the second year and the females after the third. The exploitation rate was rather high, which suggests that the rock gurnard stock was overfished in Saronikos Gulf. The male to female ratio was usually 1:1.     

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.