Age,growth, and sexual maturity of two New Zealand endemic skates,Dipturus nasutus and D. innominatus

Abstract

Rough and smooth skates (Dipturus nasutus (Banks 1841) and/), innominatus (Garrick &; Paul 1974)) were aged by counting growth bands on X‐rays of thick sections of vertebral centra. Band counts were imprecise, but there was no between‐reader bias. Age estimates were not validated. The oldest rough skate was 9 years old, but few were more than 6 years old. Females may live longer than males. The combined sexes von Bertalanffy growth curve was L_r = 91.3 (1 ‐ e^?0.16[^{t + 1.20}]). Half the males matured by c. 52 cm pelvic length (PL) and 4 years, and females by 59 cm PL and 6 years. The oldest smooth skate in the sample was 24 years, but longevity probably exceeds that. Females appear to live longer than males. The combined sexes von Bertalanffy growth curve was: L_t = 150.5 (1 ‐ e^{?0.095[t + 1.06]}). Half the males matured by c. 93 cm PL and 8 years, and females by 112 cm PL and 13 years. Smooth skate are late maturing and long‐lived relative to other skates, whereas rough skate are early maturing with a moderate life span.     

Biology of the redspotted tonguesole Cynoglossus zanzibarensis (Pleuronectiformes: Cynoglossidae) on the Agulhas Bank,South Africa

The biology of the redspotted tonguesole Cynoglossus zanzibarensis, a common African cynoglossid inhabiting the Agulhas Bank, South Africa, is described. Growth studies based on sectioned sagittal otoliths revealed that C. zanzibarensis is relatively fast-growing and long-lived, attaining ages >8 years. Growth in length was rapid in immature fish, fish attaining 56% of their maximum size within their first year. By sexual maturity, fish had attained 28% of their maximum age and 68% of their maximum length. Total length-at-age was best described by the Von Bertalanffy growth model with combined-sex growth described as L_t = 354.78(1?e^{?0.43 (t+1.17)}) mm TL. Sexually dimorphic growth patterns were evident, females attaining larger lengths, but at a slower growth rate than males. Despite the similar mean size of adult fish, the trawl-sampled adult population was dominated by females, with a sex ratio of 1 male:2.4 females. Female C. zanzibarensis mature in their second year of life (275 mm TL), after which they spawn small, pelagic eggs throughout the year. Approximations of the rates of total, natural and fishing mortality were estimated to be 0.62, 0.48 and 0.14 year^?1 respectively.     

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.     

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.     

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.     

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.     

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.     

Size trends and population characteristics of striped marlin,Tetrapturus audax caught in the New Zealand recreational fishery

Size trends and population characteristics of striped marlin, Tetrapturus audax, caught in the New Zealand recreational fishery were evaluated using club records from the Bay of Islands Sword‐fish Club (BOISC) from 1925 to 2003 (n = 15 114) and biological samples from northern New Zealand collected from 1985 to 1994 (n = 684). Average weight (kg) ± SE of striped marlin declined 6–9 kg every 20 years between 1925 (124.2 ± 1.0 kg) and 2003 (100.1 kg ± 0.4). Weight (H14843 = 444.58, P < 0.001) and condition (H443 = 37.54, P < 0.001) increased significantly throughout the recreational fishing season (December‐May). No differences were observed in the lower jaw‐fork length (LJFL)‐weight (W) relationship between sexes or years but average weight of females (106.2 ±1.1 kg) was significantly greater than males (90.2 ±1.2 kg) from 1985 to 1994 (F684 = 88.37, P < 0.001). Negative allometric growth (W = 2E ‐08 LJFL^2.88) was recorded for all striped marlin. Individual growth was modelled by fitting backcalculated LJFL to eight age classes derived from dorsal spine measurements (n = 94) using the von Bertalanffy growth equation (r² = 0.96). The parameters estimated in the von Bertalanffy growth equation were asymptotic length (L ) = 3010 mm, annual growth rate (K) = 0.22, age (yr) at hypothetical length 0 (t0) = ‐0.04.     

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.     

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.     

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 natural mortality of blue jack mackerel Trachurus picturatus (Carangidae) from the Canary Islands,Spain (NW Africa)

Status assessment of exploited fish populations is a general requirement to ensure sustainability of fisheries in both global and local contexts. The blue jack mackerel Trachurus picturatus (Bowdich, 1825) remains unassessed in a data-limited fishery in the eastern central Atlantic, within the waters of the Canary Islands (Spain) off the coast of northwest Africa. This is the most southwestern targeted fishery in the species’ distributional range. To obtain basic life-history information, a total of 2 472 specimens were analysed, ranging from 10.2 to 31.9 cm total length, from samples collected monthly between March 2005 and March 2006. Length–weight relationships (a = 0.0023; b = 3.418; R ² = 0.97) showed no significant difference between sexes. Deposition periodicity and coherence of the ageing criteria were verified by analysis of the monthly evolution of the otolith edge. Ages were estimated by counting annual growth rings on whole otoliths, with these fish ranging from age 0 to 6 years. The von Bertalanffy growth model, which was used to estimate growth parameters from both direct readings and back-calculated length-at-age data, gave good statistical fits. The parameters from the direct readings were: L∞ = 34.9 cm; k = 0.214 y^–1; t ₀ = ?2.545 y (R ² = 0.84), and the natural mortality rates estimated from empirical methods varied between 0.20 and 0.55 y^–1.     

Fish populations of the Avon‐Heathcote estuary

Characteristic organisms are tabulated, and the substrate conditions briefly described for seven habitats in the Avon‐Heathcote Estuary, Christchurch, New Zealand. Temperatures and water movements within the estuary are outlined.

From April 1965 to April 1966, samples were collected by short otter‐trawl shots, gill netting, beach seine hauls, and dip netting; the limitations of the gear are noted. The distributions and movements are recorded for nine fish species : sand flounder, Rhombosolea plebeia (Richardson) ; yellow‐bellied flounder, Rhombosolea leporina (Hutton) ; common sole, Peltorhamphus novae‐zeelandiae (Gunther) ; ye'llow‐eyed mullet Aldrichetta forsteri (Cuvier and Valenciennes); kahawai, Arripis trutta (Bloch and Schneider); spotty, Pseudolabrus celidotus (Bloch and Schneider); cockabully, Tripterygion nigripenne (Cuvier and Valenciennes) ; common bully, Gobiomorphus basalis (Gray); and globe fish, Spheroides richei (Freminville).

Length‐frequency distributions showed that most of the nine species of fish used the estuary as a feeding area for adults and as a nursery area. Only two species did not migrate to and from the sea.

Length‐weight relationships for eight species showed that weight was a function of length approximately cubed, and that the exponential equation could be used to predict weight from length.

Regressions of caudal fin length on standard length for four species gave a positive correlation (r = +0.95). Relative proportions of body length to caudal fin length were related to habitat; fish of benthic habits had proportionally shorter caudal fins than pelagic fish.     

Spawning and length‐weight of Barracouta (Teleostei: Gempylidae) from eastern cook strait

A sample of 244 barracouta, Thyrsites atun (Euphrasen), caught in eastern Cook Strait, New Zealand, between March 1966 and April 1967, was examined to determine the spawning season and length‐weight relationship.

Female barracouta ripened from April onwards, a month earlier than males. Females tended to attain maturity more rapidly than most males. October and November were the peak spawning months, although some barracouta (mainly females) were mature until January. The smallest spawning barracouta was 55 cm L.C.F. Disappearance of barracouta preceding the spawning months suggested a spawning migration.

A mathematical analysis of the length‐weight data was used to predict one value from the other, and to obtain an index of the relationship (i.e., a condition factor). There was no significant difference between the slope of the regression line n for males and females, the equations being W = 0.03867. L^2.5209 and W = 0.07391 .L^2.3687 respectively. The equation for the regression line for all barracouta, W = 0.05893 . L^2.4222, had an exponent value n lower than expected for a length‐weight relationship of unmutilated fish. The condition factor of barraoouta, measured at monthly intervals, gave a good indication of the spawning cycle.     

长牡蛎F3 代快速生长选育群体生长特性的研究

采用模型拟合方法研究了长牡蛎(Crassostrea gigas)F3代快速生长选育群体不同时期各生长性状的发育规律。结果表明,长牡蛎幼虫期壳高(SH)、壳长(SL)对日龄(t)的回归遵循Logistic模型,生长方程分别为SH=455.612/(1+9.500e-0.142t),R2=0.999;SL=462.476/(1+8.026e-0.108t),R2=0.996。幼虫期壳高与壳长成直线相关,回归方程为SL=0.76SH+18.82,R2=0.994。长牡蛎养成期各生长性状呈现明显的季节变化,壳高(SH)、壳长(SL)、壳宽(SW)和总质量(TW)对月龄(X)的多项式回归方程分别为SH=-0.0297X4+1.0365X3-12.0220X2+57.6500X-68.9260,R2=0.985;SL=-0.0173X4+0.5893X3-6.5702X2+30.2420X-34.4150,R2=0.986;SW=-0.0068X4+0.2620X3-3.2806X2+16.9170X-22.1410,R2=0.956;TW=-0.0219X4+0.8234X3-10.1680X2+50.7040X-85.4110,R2=0.972。壳高、壳长、壳宽与总质量均呈幂函数相关,回归方程分别为SH=23.645TW0.3213,R2=0.998;SL=12.337TW0.3776,R2=0.995;SW=6.611TW0.3589,R2=0.981。     

硬壳蛤形态性状与体质量、软体质量及肥满度的相关性和通径分析

为研究硬壳蛤形态性状对体质量(Y)、软体质量(Y1)及肥满度(K)的影响,测量硬壳蛤的壳长(X1)、壳宽(X2)、壳高(X3)、体质量(Y)和软体质量(Y1)等指标,并进行相关性分析、多元回归分析和通径分析。结果表明:体质量变异系数最高,壳宽与体质量相关系数最高(0.970)、壳长与软体质量相关系数最高(0.946)、壳长与肥满度相关系数最高(0.203)。壳宽对体质量直接作用最大(0.145)、壳长对软体质量直接作用最大(1.113)、壳长对肥满度直接作用最大(1.752)。形态性状与体质量、软体质量及肥满度的多元回归方程分别为Y=–46.359+0.288X1+1.723X2+0.640X3,R2=0.949;Y1=–6.607+0.301X1+0.157X2–0.161X3, R2=0.901; K=3.159+0.173X1+0.008X2–0.179X3, R2=0.072。壳宽是影响硬壳蛤体质量的主要因素,壳长是影响硬壳蛤软体质量的主要因素,各性状与肥满度回归关系不显著,个体间肥满度差异大。研究结果可为硬壳蛤选育及苗种繁育提供参考。     

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.     

Shell form,growth, and production of Astarte borealis (Schumacher, 1817) (Astartidae,Bivalvia) in the southeastern Baltic Sea

The relationships between the linear dimensions and body weight and the ratio between the masses, growth, and production were studied for the bivalve Astarte borealis inhabiting the southeastern Baltic Sea. The maximal shell length was 21.09 mm, while the maximum age was 8+. The linear growth was described by the Bertalanffy equation L _τ = (1 - e ^{-0.0894(τ-(-0.7354))}). The annual production was 7.60 kJ/m² at a P _s/B coefficient of 0.41. It was found that the A. borealis inhabiting the southeastern Baltic Sea was characterized by a lower linear growth rate compared to the mollusks of other parts of the geographical range due to the low salinity of the Baltic Sea.     

福建泉州山美水库翘嘴红鲌(Erythroculter ilishaeformis)生长特性、资源评估与合理利用

随机从福建泉州山美水库2002年4月—2003年5月的翘嘴红鲌(Erythroculter ilishaeformis)渔获物中获取340尾样本,以鳞片为年龄鉴定材料,获得年龄生长资料,建立生长方程和Beverton-Holt模型对山美水库翘嘴红鲌资源进行评估,为制定合理的捕捞年龄和捕捞规格提供科学依据。结果表明,山美水库翘嘴红鲌体重范围是0.035—4.12kg,体长范围是15.6—73.5cm,其中体长20.1—60.0cm的样本占93.57%,且为2+—3+龄。本文给出了该鱼类体长与体重的关系式、体长与鳞径的关系式以及相关的von Bertalanffy方程。山美水库翘嘴红鲌生长拐点为10.4龄,山美水库现有资源量为10.164t,合理开捕年龄为6龄。     

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.