Growth,sexual maturity and reproduction in the hottentot Pachymetopon blochii (Val.)

The growth of hottentot is described by the relationship L_f (mm) = 538,015 (1?e^{?0,097(t + 0,431)}). By determining the otolith growth rate and validating it with counts of daily rings identified on scanning electron micrographs of otolith sections, it was found that previous growth curves underestimated the age of the fish by one year. Differences in growth rate between sexes and over geographical regions were negligible. The ratio of males to females in sampled catches was 1:1,383 and 50-per-cent sexual maturity was attained at 220 mm fork length. There are two main spawning seasons, late autumn and summer, although some breeding activity continues throughout the year. Spatial differences in mean gonadosomatic indices were minimal.     

A preliminary study of age and growth of the monkfish Lophius upsicephalus (Pisces: Lophiidae) on the Agulhas Bank,South Africa

The sagittal otoliths of Lophius upsicephalus, although extremely variable in shape, were found to be the only structures suitable for age estimation. The annuli are multi-ringed zones separated by "wider than normal" opaque zones. They are difficult to interpret, especially those of fish older than nine years. Periodicity of annulus formation could not be determined by standard methods. By inference, annulus formation could be related to feeding habits and reproductive seasonality. The growth in length (sexes combined) is best described by

Length-at-age = 733,7 (1 – e^{?0,1054 (t + 1,879)})mm.

There is a significant difference in growth by mass between the sexes. The respective equations describing growth by mass (in g) for males and females are:

Weight-at-age = 8616 (1 – e^{?0,1054 (t + 1,879)})^2,805 and

Weight-at-age = 9499 (1 – e^{?0,1054 (t + 1,879)})^2,890.     

Growth of red gurnard (Teleostei: Triglidae) from Pegasus bay,Canterbury, New Zealand

Growth of the red gurnard, Chelidonichthys kumu (Lesson and Garnot), from Pegasus Bay, Canterbury, was measured during 1966–67. Otoliths were used as an indicator of fish growth; mean length‐at‐age data were obtained from back‐calculated fish lengths at the time of formation of successive annual rings in the otoliths. Growth in length was found to be adequately expressed by the von Bertalanffy growth equation :

l_t = 52.0 [1 ‐ e‐^{0.406 (t‐o.291)}]

(where l_t is the fork length in cm at age t). The length: weight relationship was:

w = 78.56 × 10^‐4 l ^3.072

(where w is the weight in grams). From this relationship, growth in weight was described by the equation:

w_t = 1469 [1 ‐ e‐0.406 (t‐0.291)]³.     

Growth of Cape horse mackerel Trachurus trachurus capensis off South Africa

Recent studies have provided evidence that the Cape horse mackerel Trachurus trachwus capensis in South African waters is a unit stock. Therefore, an age and growth study of the entire stock throughout its distributional range was undertaken in 1988/89. Growth is described by the equation

L_t = 487,989 (1 – e^{?0.556(t – 0,229)}) mm.     

Growth of spotted ragged-tooth sharks Carcharias taurus (Rafinesque) in captivity

Eight spotted ragged-tooth sharks Carcharias taurus (95–248,4 cm total length TL), ranging in known age from 0 to 16,6 years, were used to investigate the growth of the species in captivity. Total length was measured by a standard technique in some cases and estimated from photographs in others. The accuracy of the photographic technique was evaluated and found adequate for captive growth studies in sharks. Parameters of various growth models were estimated by non-linear regression and the special Von Bertalanffy growth model provided the best fit to the age-length data of the combined sexes. The parameters of the special Von Bertalanffy model are L _∞ = 249,8 cm TL, K = 0,233·year^?1, t ₀ = ?2,238 years. Longevity of captive C. taurus is greater than 16,6 years.     

The biology,life history and management needs of a large sciaenid fish,Argyrosomus coronus,in Angola

The West Coast dusky kob Argyrosomus coronus is an understudied yet important fishery species in Angola. During a five-year study (2005–2009), the species was recorded in all fishery sectors, but was most important in the inshore recreational fishery in southern Angola (Cunene Estuary to Namibe). Early juveniles (<300 mm total length, TL) were captured in the offshore artisanal fishery at Praia Pinda, whereas juveniles (300–600 mm TL), subadults (600–870 mm TL) and adults (>870 mm TL) were captured in all fisheries as far north as Namibe, and shoals of large adult fish (>1 000 mm TL) were occasionally captured in the offshore purse-seine commercial fishery between the Cunene Estuary and Lucira. Because some Argyrosomus species are morphologically cryptic, a DNA barcoding method was used to confirm the taxonomic status of the biological samples used in this study. The male:female sex ratio of examined samples was 1:1.4 (n = 225). The length-at-50% maturity was 823 mm and 904 mm TL for males and females respectively. Age-at-50% maturity was 4.4 and 4.3 years for males and females respectively. The periodicity of otolith ring formation was confirmed to be one year using a marginal zone and a chemical marking analysis. Growth (in mm TL) was best described by: L_t = 1 826(1—e^{?0.12(t + 1.60)}). Argyrosomus coronus fed predominantly on fish, mainly Sardinella aurita (62% frequency of occurrence). Early juveniles appeared to frequent the offshore zone (50–100 m depth), moving into the inshore region at approximately 300 mm TL. Juveniles and subadults were resident (57% recaptured at the same site) and were particularly abundant around the mouth of the Cunene Estuary as well as in central and northern Namibia. Adults undertake migrations that correspond with the movement of the Angola–Benguela frontal zone, moving north as far as Gabon in winter and returning to southern Angola in spring, when spawning appeared to take place offshore. There are currently no catch restrictions on A. coronus in Angolan waters. However, declining catches and increasing fishing effort suggest that some management intervention is required, commencing with a proposed closure of the Cunene Estuary mouth region to fishing.     

Age and growth of Cape stumpnose Rhabdosargus holubi (Pisces: Sparidae) in the Eastern Cape,South Africa

Rhabdosargus holubi is a small (maximum weight=2.4?kg) yet important fishery species in the estuaries of the south-east coast of South Africa. Little is known of its biology and specifically its growth rate, which is essential for sustainable management of the fishery. We examined and counted the opaque zones in the sectioned otoliths of 134 R. holubi to determine its age and growth parameters. The otoliths from two recaptured fish marked with oxytetracycline confirmed that one opaque zone was deposited annually. The species reached a maximum age of 18 years and growth was adequately described by a von Bertalanffy growth function of the form: L_t = 358.1 (1 – e^{?0.24(t+0.77)}) mm fork length. There were no significant differences between any of the male and female growth parameters (likelihood ratio test: p = 0.3). The growth was slow (omega index: ω = 86.56); however, despite this, the unique life history of R. holubi may provide a degree of resilience to heavy fishing pressure in estuaries.     

Life history of white stumpnose Rhabdosargus globiceps (Pisces: Sparidae) off South Africa

Fishery-dependent and fishery-independent distribution analyses together reveal four discrete areas of white stumpnose Rhabdosargus globiceps abundance between Port Nolloth and the Kei River off the Cape Province of South Africa: the Western Cape (Saldanha Bay), the South-Western Cape, the Southern Cape and the South-Eastern Cape. On the basis of migratory patterns determined from tagging and catch data, and on differences in growth rate and size-at-maturity, it is concluded that these areas of abundance represent four separate stocks. Each stock apparently disperses offshore in winter (to c. 130 m depth) and concentrates inshore (<60 m depth) in response to ocean ographic patterns during summer. Growth rate and size-at-50% maturity (L ₅₀) increased clinally from the South-Eastern Cape through to the South-Western Cape, and in all three regions males matured at larger size than females. Sizes at maturity for male and female R. globiceps were respectively 18.6 and 15.3 cm (fork length, FL) in the South-Eastern Cape, 22.1 and 18.1 cm in the Southern Cape and 24.3 and 23.6 cm in the South-Western Cape. The fitted Von Bertalanffy growth equations for the three regions were: L_t = 349 (1?e^{?0.114(t+3.60)}) mm for the South-Eastern Cape; L_t = 337 (1?e^{?0.207(t+1.05)}) mm for the Southern Cape; and L_t = 379 (1?e^{?0.290(t+0.16)}) mm for the South-Western Cape. Maximum ages recorded in each region were 21 years for the South-Western Cape, 20 years for the Southern Cape and 10 years for the South-Eastern Cape. Lack of older fish in the South-Eastern Cape sample, attributed to inadequate sample size, has probably resulted in overestimates of both L _∞ and K in this region. Spawning is from August to February, with a peak in spring (September–November). Early juvenile R. globiceps recruit into estuarine and surf-zone marine nursery areas at around 2–5cm (±3 months), but move progressively farther offshore with growth; those trawled deeper than 50 m east of Cape Agulhas were predominantly adults (20–35 cm FL). Because of cooler water temperatures west of Cape Agulhas, adults there are found from the surf zone to depths of only 20 m in summer.     

Life history of Plesionika edwardsi (Crustacea,Decapoda, Pandalidae) around the Canary Islands,Eastern Central Atlantic

The life history of Plesionika edwardsi (Brandt, 1851) around the Canary Islands in the Eastern Central Atlantic was investigated, based on a total of 11 434 shrimps ranging in length between 8 and 40 mm carapace length (CL). The species carries out seasonal migrations; they concentrate in deep water during winter, move shallower in summer and return to deep water again in autumn. Ovigerous females occur throughout the year, but a spawning peak was determined between April and September. The size at maturity for females was approximately 26 mm CL. Shrimp size generally increased with increasing water depth. The growth parameters for males were L _∞ = 25.75 mm CL and K = 0.55 year^?1, and L _∞ = 28.28 mm CL and K = 0.66·year^?1 for females. The species displays the typical reproductive pattern of tropical pandalids and is dioecious.     

Growth and reproduction of the Japanese mantis shrimp, <Emphasis Type="Italic">Oratosquilla oratoria</Emphasis> (De Haan 1844) in the coastal area of Tongyeong,Korea

Growth and reproduction of the Japanese mantis shrimp, Oratosquilla oratoria, were investigated in the Tongyeong, Korea from July 2014 to August 2015. A total of 2,621 samples (1,380 females and 1,241 males) were collected during the study period. Females were observed more frequently than males. The mean body length (BL) was 128.5 ± 0.38 mm in females and 126.9 ± 0.42 mm in males. The mean body weight (BW) was 31.2 ± 0.28 g in females and 31.1 ± 0.32 g in males. There was a significant difference in the length-frequency distribution between females and males. The relationship between BL and BW was lnBW = 2.85 × lnBL - 10.43 for females and lnBW = 2.87 × lnBL -10.52 for males. The gonadosomatic index (GSI) varied on a monthly basis. The GSI reached a maximum in May and a minimum in November. The highest values of the GSI coincided with the spawning period of O. oratoria. Larger individuals of O. oratoria have their spawning season earlier than smaller ones. The size at sexual maturity of females was estimated as 96.5 mm. The Von Bertalanffy growth function parameters were BL_∞ = 184.5 mm, K = 0.72 year^?1, C = 0.36 and WP = 0.45 for females and BL_∞ = 183.75 mm, K = 0.82 year^?1, C = 0.38 and WP = 0.22 for males. The growth of males was slightly faster than females. The present study will help with the fisheries management of O. oratoria based on ecological parameters.     

Age and growth of bluenose,Hyperoglyphe antarctica (Pisces: Stromateoidei) from the lower east coast,North Island,New Zealand

Growth of the bluenose, Hyperoglyphe antarctica (Carmichael, 1818) from the lower east coast, North Island, was determined by counting growth check rings in otoliths. One growth check ring appeared to be laid down each year, so this technique is probably valid for aging bluenose. Female fish had a significantly higher growth rate than males. Comparisons of samples from three sites indicated no significant regional differences in growth. The von Bertalanffy parameters L8,K, and t0 fitted to back‐calculated fish lengths were, respectively, 81.1 cm, 0.308, ‐0.627 for males, and 86.1 cm, 0.308, ‐0.384 for females.     

Relationship between somatic growth and otolith growth: a case study of the ornate jobfish Pristipomoides argyrogrammicus from the coast of Réunion (SW Indian Ocean)

The ornate jobfish Pristipomoides argyrogrammicus Valenciennes 1832 occurs in the Indo-West Pacific Ocean, where it is harvested by small-scale coastal fisheries. Management of this species is hindered by lack of adequate biological data. We sampled a total of 113 individuals from the landings of local artisanal fishers on the island of Réunion (southwestern Indian Ocean), from March 2014 to March 2015. The relationships between two types of body length (total and standard length, cm) and total weight (g) were shown to be significant (p < 0.05). The length–weight relationship was described by a power function, with the scaling factor estimated to be 0.008 and the exponent 3.146. Age was determined using whole otoliths. The von Bertalanffy growth equation was estimated to be TL_t = 30.68(1 – e^?0.52(t)). Otolith morphometry variables (length, width and area) were significantly correlated with age estimates (p < 0.05). No significant difference in age estimates was observed between left and right otoliths used as predictors. Readings from observed age and the estimates from modelled age indicated relatively good agreement, suggesting the potential to use whole otoliths for age estimation.     

Age, growth and reproduction of the sand smelt Atherina boyeri Risso, 1810 in the Gomishan wetland – southeast Caspian Sea

A total of 2256 specimens of Atherina boyeri caught in Gomishan wetland (a marsh lagoon located at the southeast Caspian Sea) during spawning season from February to August 2007 were examined for life-history attributes. The population has a 4-year life cycle. Length–weight relationship was estimated as W = 0.0053TL^3.0181 for males and W = 0.0050TL^3.063 for females, being allometrically positive for both sexes. The von Bertalanffy growth function fitted to back-calculated size at age data was: Lt = 155.17[1 − exp − 0.28(t + 0.738)] and Lt = 162.77[1 − exp − 0.27(t + 0.727)] for males and females respectively. The sex ratio was 1:1.30 in favor of females. The reproductive season, evaluated from GSI, extended from March to July, with a peak in March. The average absolute and relative fecundities were 2976 eggs and 874 eggs g⁻¹ of body weight respectively. The diameter of oocytes ranged from 0.03 to 0.20 mm with a mean value of 0.68. The life-history patterns of A. boyeri in the population under study imply that the population of this species in the southeast Caspian Sea differs markedly from those of other localities of its range distribution. The differences were thought to be due to differences in geographical locations.     

Aspects of the biology and fisheries of an economically important sparid Dentex macrophthalmus (Bloch 1791) in the Namibe province,Angola

The sparid Dentex macrophthalmus is a widespread, important fishery species along most of the West African coast from southern Namibia to the Mediterranean. In southern Angola it is an important artisanal species targeted predominantly by handline fishers. A biological and fisheries study was conducted on this species in southern Angola between June 2008 and July 2009. It was the dominant species in the artisanal fishery, accounting for 99% of the sparids captured and 67% (by mass) of the total catch. The life history of D. macrophthalmus was characterised by slow growth (females: L_t = 309[1 ? e^{?0.06(t + 5.43)}], males: L_t = 248[1 ? e^{?0.16(t ? 1.77)}]), advanced age at maturity (females: 7.4 years, males: 6.0 years) and high longevity (females: 36 years, males: 38 years). The sex ratio was 1:1 male:female. The length- and age-frequency distributions and macroscopic observations suggested that the species is a late gonochorist. Males and females reached 50% maturity at 151 and 166 mm fork length respectively. Although individuals with ripe gonads were found during most of the year, the peak spawning period appeared to be in December and January. Despite a life history that renders D. macrophthal-mus vulnerable to overexploitation, only 38% of artisanal fishers noticed a decline in the catches of this species. Potential reasons for this include: technology creep; limited pressure on the juvenile portion of the stock as a result of late recruitment (above the length of 50% maturity); the ‘basin affect’, whereby depleted areas are reseeded by areas (e.g. deeper water) inaccessible to the linefishery; and a deep-water reserve of large individuals. It is recommended that precautionary management strategies be implemented until the age estimates are revised by the countries in which this species forms significant fisheries.     

Age and growth of narrow-barred Spanish mackerel Scomberomorus commerson in the coastal waters of southern Mozambique and KwaZulu-Natal,South Africa

The narrow-barred Spanish mackerel Scomberomorus commerson is one of the most important linefish species caught in KwaZulu-Natal and southern Mozambique waters, forming the basis of important commercial, artisanal and recreational fisheries. A total of 439 S. commerson were sampled along the east coast of southern Africa (KwaZulu-Natal, South Africa, and southern Mozambique) between April 2011 and March 2012. Retrospective length-at-age data observed from whole otoliths were used to compare and describe sex-specific growth. Growth rates obtained from otolith-derived data were compared with those estimated from 29 tag-recaptured fish. Overall, ages ranged from 0.48 to 14.6 years for females and 0.4 to 13.57 years for males. Otolith readings yielded an average percent error of 11.21%, lower than recorded in a previous study from the region. Marginal zone analysis provided strong evidence that one translucent and one opaque growth zone were laid down annually. Schnute growth-function parameters indicated significant differences in growth between sexes. Females approached their mean asymptotic length at a faster rate, and grew to a greater mean length-at-age, relative to males. Growth in both sexes was rapid, achieving 67.46 cm FL (females) and 65.4 cm FL (males) in their first year of life. Growth rates obtained from tag-recaptured S. commerson indicated slower growth for smaller/younger fish up until 70 cm FL after which growth was very similar to that observed from otolith-derived data. The results of this study provide accurate, validated life-history parameters for king mackerel that are important for the assessment of stock status in the region.     

The biology of the catfish Cnidoglanis macrocephalus (Plotosidae) in an Australian estuary

This paper describes the age structure, growth, diet and aspects of gonadal development in the cobbler, Cnidoglanis macrocephalus (Valenciennes), in the large Swan estuary in south-western Australia between August 1982 and June 1984. Analysis of otolith annuli showed that while the 0+ to 3+ age classes were regularly represented in monthly samples, the 4+ and more particularly the 5+ and 6+ were much less abundant. The weighted means for the back calculated lengths at the end of the first to fourth years of life were 181 mm (≡ 26 g), 314 mm (≡ 156 g), 418 mm (≡ 410 g) and 518 mm (≡ 833 g) respectively. The mean length at the end of the second year of life was similar to the minimum legal size for capture by commercial fishermen (320 mm). The von Bertlanffy growth curve calculated from the back calculated lengths was L_t = 917 [1 − e^{−0·20(t + 0·11)}]. The relative weight of mulluscs, crustaceans and polychaetes in the intestine varied markedly between small and large fish, apparently reflecting differences in the size of these prey. The large mean diameter of mature eggs ( ) was correlated with a low mean absolute fecundity (2078). Trends shown by egg size, gonadosomatic index and time of appearance of spent females indicate that spawning takes place between October and December. The attainment of sexual maturity is both age- and size-dependent. Although sexually maturing and occasionally spent fish were found in the lower estuary, meristic values, commercial catch statistics and other data indicate that the cobbler found in the Swan estuary are part of a population which typically spawns at sea.     

Age and growth of two populations of West Coast steenbras Lithognathus aureti in Namibian waters,based on otolith readings and mark-recapture data

Age and growth of West Coast steenbras Lithognathus aureti, sampled from two separate populations (northern and southern) along Namibia's coast, was determined using sectioned otoliths, and the results were validated using mark-recapture data. For both populations, the special three-parameter Von Bertalanffy growth model described growth adequately. Growth of the southern population was described by the equation L_t = 73.556(1?e^{?0.065(t+3.92)}) cm and for the northern population by L_t = 84.601(1?e^{?0.088(t+2.756}) cm. Environmental conditions, such as difference in sea surface temperature, density-dependent competition for food, or biochemical genetic variations between the two populations, are possible reasons for the geographic differences found in the growth rates and length-at-age. Slow growth and longevity are characteristics of West Coast steenbras that make it extremely susceptible to overfishing; careful management of the resource is therefore essential.     

Age and growth of redeye round herring Etrumeus whiteheadi off the South African coast

Ages of redeye round herring Etrumeus whiteheadi were estimated with associated errors and used to infer life-history information, such as age composition, age-at-maturity and instantaneous mortality rate. Samples were collected in November 2005 during a research survey aimed at estimating the biomass of spawning pelagic fish off South Africa’s west and south coasts. Replicate age estimates obtained from sagittal otoliths were collected with slight bias and relatively high precision. A von Bertalanffy model describing growth of the combined sexes, including juveniles, was L_t = 20.41(1 ? e^{?0.41(t ? 1.92)}). Kimura’s likelihood ratio test revealed no statistically significant differences between growth parameters of males and females. Results suggested that otolith length is a better predictor of age than otolith weight. Maturity estimates for E. whiteheadi were similar to those previously documented.     

Growth discontinuity in males of the deep-water giant red shrimp Aristaeomorpha foliacea in the Mediterranean Sea

The deep-water giant red shrimp, Aristaeomorpha foliacea (Risso, 1827) (Decapoda, Aristeidae), represents a highly valuable resource for bottom trawling in the Mediterranean Sea. Recent assessments have described both a worsening of the status of the traditionally exploited stocks and low levels of annual-based instantaneous natural mortality (M 0.4–0.7 year⁻¹) in the unexploited stocks. The mortality (M) figures, however, are in contrast with the longevity (T_max) of 3–4-year males and 4–5-year females, estimated from classical length frequency distribution analysis. Reduced growth (after the onset of sexual maturity) and pile-up of older individuals in the larger size classes have been considered to be reasonable explanations for the contrast between M and T_max. We propose that a discontinuity of the growth models could address this contrast. Because a clear discontinuity in sexual maturity is evident only in males, length frequency distribution data for different sets of males collected from the South of Sicily and the Maltese Islands deep bottoms (400–800 m) were fitted with both the classic (c) and double-phased (d) von Bertalanffy growth formula (VBGF). According to the dVBGF, adult males sharply reduce their growth rate after reaching an age between 1.2 and 1.5 year, which corresponds to the estimates of age at sexual maturity (t_m between 1 and 1.5 years). The reduction in growth determines a higher T_max (7.3–9.5 year) and lower M (0.4–0.6 year⁻¹) than previously derived on the basis of cVBGF estimates (T_max 3–4 years and M 1.2 year⁻¹). The dVBGF results suggest that sexual dimorphism and length–sex segregation in giant red shrimps reflect an alternative life history strategy that is based mainly on growth reduction in adult males and it might be adopted for implementing more conservative assessments.     

Biology and Population Dynamics of Donax trunculus L. (Bivalvia: Donacidae) in the South Adriatic Coast (Italy)

Biology and population dynamics of the suspension-feeding wedge clam Donax trunculus (Linnaeus, 1758) were studied for 13 months (November 1994–April 1996) along the Italian Southern Adriatic coast near the Lagoon of Lesina. Specimens were found at depths between 0 and 2 m, mainly in fine grain bottoms. The spatial coastal distribution showed an intraspecific segregation between young and adult wedge clams. A unimodal recruitment (length >4 mm) occurred in winter (December–February). Length frequency distributions were used to determine age and growth rate. Three year classes were regularly observed and their growth pattern defined. The population showed a maximum length of 37 mm and a longevity of 4 years. Analysis of seasonal variations in the reproductive cycle showed that gametogenesis occurred in spring in females. After the spawning season (March–July) females of D. trunculus remained in a resting stage from August to January.