Age and growth of the duckbill catfish (Sorubim cf. lima) in the Pantanal.

The Duckbill Catfish, Sorubim lima, is a predator of large South American rivers. The age and growth of S. lima were studied based on the pectoral fin-spines of samples collected from the Cuiabá River, Pantanal. The samples were taken from commercial and experimental hook-and-line fishing. An analysis of the marginal increment suggests that the growth rings are formed once a year during the dry season, from July to September (ANOVA type I: F = 4.183; g.l. = 3 and 104; p = 0.008). The estimate of the parameters that describe von Bertalanffy's growth curve by nonlinear regression of the observed lengths in the age were: L infinity = 56.0 cm (fork length); k = 0.245 year-1; to = -2.605 years. The animals were estimated to have a life span of 9.6 years. The findings indicate that the fork length is a good predictor of the age of individuals of this fish species.     

Age and growth of albacore Thunnus alalunga in the North Pacific Ocean

The age and growth of North Pacific albacore Thunnus alalunga were investigated using obliquely sectioned sagittal otoliths from samples of 126 females and 148 males. Otolith edge analysis indicated that the identified annulus in a sagittal otolith is primarily formed during the period from September to February. The assessments of the fish age at first annulus formation indicated that the first annulus represents an age of <1 year. This study presents an age estimate (0·75 years) for the formation of the first annulus. The oldest fish ages observed in this study were 10 years for females and 14 years for males. The von Bertalanffy growth parameters of females estimated were L(∞) = 103·5 cm in fork length (L(F) ), K = 0·340 year(-1) and t(0) = -0·53 years, and the parameters of males were L(∞) = 114·0 cm, K = 0·253 year(-1) and t(0) = -1·01 years. Sexual size dimorphism between males and females seemed to occur after reaching sexual maturity. The coefficients of the power function for expressing the L(F) -mass relationship obtained from sex-pooled data were a = 2·964 × 10(-5) and b = 2·928.     

Validation of the periodicity of increment formation in the otoliths of a cichlid fish from Lake Tanganyika, East Africa

Tetracycline was used as a chemical tag in a mark‐recapture study to examine the pattern of increment formation in the otoliths of Tropheus moorii , a rock‐dwelling cichlid from Lake Tanganyika. A total of 256 fish were captured by divers and injected with tetracycline. Of these, nine were recaptured after either 1 or 2 years at liberty and eight retained tags within their otoliths. Comparison of the number of growth increments formed after the tag and the time at liberty demonstrated that increments were deposited on an annual basis in the otoliths of this species. Furthermore, there was a strong relationship between otolith mass and age suggesting that otoliths grew at a predictable rate throughout the life of the fish. Validation of an annual pattern of increment deposition allowed age and growth information to be derived from otoliths. This showed that T. moorii grew rapidly to attain adult size by 3 years of age. Males grew faster than females and also attained a larger size than females (8·74 v . 7·91 cm L _S respectively). The longevity of some of these small freshwater fish was surprising; the oldest individual had an age of 10 years, while the average age of adults was 4 years.     

Age and growth analysis of the mosshead sculpin Clinocottus globiceps Girard 1857 (Pisces: Cottidae) from Helby Island, British Columbia

The age and growth of the cottid fish Clinocottus globiceps Girard from tidepools at Helby Island, British Columbia, Canada were investigated with the aid of whole saccular otoliths (sagittae); ages were validated by marginal increment analysis. Four hundred and twenty five specimens were examined from 214 females and 211 males. Marginal increment analysis on specimens with one to three opaque zones suggested an annual ring deposition in sagittae during the late autumn and spring months.
The C. globiceps population was composed of individuals from less than 1 year to 5 years of age for fish measuring between 5–120 mm standard length. Growth was faster for younger than for older age groups. Lengths-at-age data were fitted to the Gompertz growth model, and estimates of the model parameters L₀, G and g were 26.7 mm 1.58 and 0.30 for pooled cohorts, respectively. The highest levels of growth occurred during late spring and early summer, when water temperatures were at maximum and food was most abundant. The lowest levels of growth occurred during the autumn and winter months.     

Condition and size of the non‐native pikeperch Sander lucioperca (Linnaeus, 1758) in Portuguese river basins

We studied life‐history traits focusing on the growth and condition of the pikeperch Sander lucioperca to evaluate its phenotypic plasticity when introduced to new environments. Pikeperch is a non‐native fish introduced to Iberian freshwater fauna in 1998 that quickly spread to other river basins through human‐mediated activities, occupying now a wide variety of habitats along mainland Portugal. Condition (K and SMI), fork length at age, and length–weight relationships were studied for Portuguese populations. Pikeperch fork length for ages 1, 2, 3, and 4 was different between several populations. We applied generalized linear models (GLM) to study the influence of habitat type, latitude, altitude, time after first detection, and fish prey richness on pikeperch populations size at age 4 and condition. We observed higher condition values on populations from lower altitudes at lentic systems more recently introduced. But higher fork length at age 4 was found in populations from higher altitudes, on older populations with higher prey richness. Habitat type, time since first detection, and fish fauna composition are discussed as the main environmental factors explaining the observed phenotypic plasticity with concerns on predatory impact on native fauna.     

Sex-biased dispersal and growth in sablefish (Anoplopoma fimbria) in the northeastern Pacific Ocean

To examine the potential linkage between sex-biased growth and dispersal in demersal fish, we studied the movement distance and growth of tag-recaptured sablefish (Anoplopoma fimbria). Tagging was conducted by teams from Japan and the United States. From 1980 to 1984, 58,918 sablefish were captured by Japanese vessels and tagged with anchor tags, and between 1980 and 2007, 3319 sablefish were recaptured in the Bering Sea and northeastern Pacific. Of these 3319 fish, we analyzed data on 659 individuals for which we have reliable data on recapture location, sex and fork length at the time of release and recapture, and elapsed time longer than 10?days. Annual growth increments (mean±S.D.) were 2.5?±?6.5?cm (males) and 3.5?±?8.6?cm (females), and the movement distances (assumed to be straight) were 712?±?800?km (males) and 877?±?920?km (females). Females grew larger and moved longer distances than males. We calculated the growth increment deviation that accounted for the effects of elapsed time, curvilinear growth, and initial fork length at release using a von Bertalanffy growth model. The growth increment deviation increased significantly with the distance moved over elapsed time. In addition, the relationship between distance moved over elapsed time and the growth deviation differed significantly between sexes; females grew faster than males at a given movement distance. We suggest that female-biased dispersal is a factor generating female-biased growth in sablefish.     

Growth parameters estimates for a small fish of the Pantanal, Brazil: Moenkhausia dichroura (Characiformes; Characidae).

Growth parameters were estimated for Moenkhausia dichroura (Kner, 1858) (Characiformes, Characidae), a small-sized and very abundant fish of the Pantanal lentic habitats commonly known as "pequira ". A method based on the length frequencies distribution and the ELEFAN I routine from the FISAT program were used. The fish were collected in the Baia da On?a, an oxbowlake of the sub-region Pantanal of Aquidauana, Mato Grosso do Sul, Brazil, from June to December 1988. The standard length of the captured fishes ranged from 29 to 76 mm with an average of 53 mm. The estimated growth parameters were L(infinity) = 81 mm (standard length), k = 0.85 year(-1), C = 0.89, WP = 0.6 (Rn = 0.285). The WP indicated that growth reduction occurred in July, when the lowest temperature of the year was registered. The growth curve showed that captured individuals belonged to three cohorts. The obtained results seem robust and quite compatible with the biology of the fish and its adjustment to the environment. M. dichroura, in spite of not being a direct fishing interest, is an important species in terms of its ecological aspects, due to its abundance and high growth rate, and as a great food source for aquatic organisms and specially for larger fish of economic value. Considering the information gap about small fish, the parameters estimated for pequira constitute a comparison base for other growth studies of small-sized fish species of tropical environments.     

The growth of Tilapia mossambica Peters (Pisces: Cichlidae) in Lake Sibaya, South Africa

The scales of Tilapia mossambica Peters * from Lake Sibaya show clear rings formed by broken, widely-spaced circuli in the anterior field. In order to determine the rate and time of scale ring formation, the number of circuli in the marginal increment was determined. Five scales from the pectoral region of 2223 fishes caught at regular intervals over two years were examined. When plotted as histograms, the number of circuli in the marginal increment showed a sharp movement to the left in September–October and again in January, indicating that the rings were formed during these months in the majority of fish examined. Pre- and postbreeding feeding migrations, and increases in condition factor, were associated with scale ring formation. Otoliths and opercula were also examined for age determination. Annual length increments were calculated for 450 T. mossambica collected throughout the year, and growth curves plotted. T. mossambica from Sibaya reach maturity after one year at a standard length of about 8 cm in females, and after two years at 10 cm in males. The breeding population had a standard length mode of 11–12 cm in females and 17 cm in males. The maximum final size was about 24 cm.     

Age‐based demographics of the pearl perch Glaucosoma scapulare (Ramsay, 1881)

This research represents the first age‐based demographic assessment of pearl perch, Glaucosoma scapulare (Ramsay, 1881), a highly valued species endemic to coastal waters off central eastern Australia. The study was conducted across the species' distribution that encompasses two state jurisdictions (Queensland in the north and New South Wales in the south) using data collected approximately 10 years apart in each state. Estimates of age were made by counting annuli (validated using marginal increment ratios) in sectioned sagittal otoliths. The maximum estimated age was 19 years. Pearl perch attained approx. 12 cm fork length (FL) after one year, 21 cm FL after 2 years and 29 cm FL after 3 years. Fish from the southern end of the species' distribution grew significantly more slowly than those from the northern part of its range. Commercial landings in the north were characterized by greater proportions of larger (>40 cm FL) and older (>6 years) fish than those in the south, with landings mainly of fish between 3 and 6 years of age. The observed variations in age‐based demographics of pearl perch highlight the need for a better understanding of patterns of movement and reproduction in developing a model of population dynamics and life‐history for this important species. There is a clear need for further, concurrent, age‐based studies on pearl perch in the northern and southern parts of its distribution to support the conclusions of the present study based on data collected a decade apart.     

Age and growth of the spotted goatfish, Pseudupeneus maculatus (Bloch, 1793) in Brazil, validated through marginal increment and oxytetracycline dyes in the sagittae

A sample composed of 4973 specimens of the spotted goatfish, Pseudupeneus maculatus (4.5–29.2 cm fork length) was collected off northeastern Brazil from 1999 to 2002. Sagittae (398) were analyzed for age and growth estimation using both annuli and microincrements. For the first approach, the mean monthly marginal increment ratio analysis suggested that one band is formed annually from May to June. With the microincrements analysis, 15 specimens were reared (3–71 days) for validation of periodicity using oxytetracycline. Fluorescent dyes were observed in 10 specimens (7.5–16.9 cm). After testing, one microincrement was found to form daily. Otolith sections were polished and analyzed using a light microscope (100–1200× magnifications). Individuals larger than 22.6 cm (4 years) showed heavily overlaid increments on the otolith edge, which hampered the counts. There was agreement on the size from counts on an annual and daily basis. The von Bertalanffy function provided the following parameters: L_∞ = 33.23 cm; K = 0.265; t₀ = 0.0883 year. The sample was composed of 0⁺ to >5‐year‐old specimens. Age at first maturity was 3.6 years (20 cm), whereas the recruitment age for fisheries was 3.9 years. Juveniles represented about half of the catch (48.7%), which may have implications for population equilibrium.     

Comparison of growth rate and formation of otolith increments in age-0 red snapper

For wild red snapper Lutjanus campechanus , mean otolith increment deposition rate after marking with oxytetracycline dihydrate (OTC) was daily (0.97 increments day⁻¹) when growth rates were fast (0.63 mm fork length, L _F day⁻¹), but were not daily (0.82 increments day⁻¹) when somatic growth was slow (0.2 mm L _F day⁻¹). For reared larvae ( n =8), increment deposition rates were daily (0.99–1.03 increments day⁻¹), and growth rates ranged from 0.6 to 0.9 mm L _F day⁻¹. Growth rate affected increment deposition rate as a threshold function, i.e. when growth rate was <0.3 mm L _F day⁻¹, deposition was less than daily, but above this level increment deposition did not exceed a daily rate. As growth rates increased increment widths increased. Examination of a sub-sample ( n =8) of the otoliths from the slowest growing wild fish by scanning electron microscopy did not increase increment counts. Because L. campechanus are late spring-early summer spawners, young fish can expect maximum growth due to warm summer temperatures. Thus, daily ageing methods should be well suited to this species.     

Life-history strategies of Acrossocheilus fasciatus (Barbinae, Cyprinidae) in the Huishui Stream of the Qingyi watershed, China

Life-history traits of Acrossocheilus fasciatus were examined using 384 specimens collected monthly during May 2009 and April 2010 in the Huishui Stream of the Qingyi watershed, China. Using scales for age determination, female and male fish comprised five and four age groups, respectively. The monthly changes in marginal increment ratio suggested that annuli on scales were formed during March through May. Total lengths back-calculated significantly increased with age for both sexes and varied significantly between the two sexes at each age. The fact that females had larger body size and grew faster than males indicated the sexual size dimorphism for this species. Both sexes got their 50% maturity at age 3, when females and males were 105.3 and 112.1?mm total length, respectively. Based on the monthly changes in the gonado-somatic index and egg-development process, fish spawned from April through August. Absolute fecundity ranged from 295 to 3,573 eggs per fish and increased significantly with age. But relative fecundity, ranging from 11.77 to 69.96?eggs/g, was not significantly different among age groups. Compared with the life-history traits of an upstream population in the Puxi Stream (a headwater stream within this study watershed), the downstream population of A. fasciatus in the Huishui Stream (a 4th-order stream) exhibits larger body size, faster somatic growth, later sexual maturity, and lower reproductive investment. These variations in life-history strategies between the two populations could perhaps be explained by the spatial heterogeneity in habitat environment along the upstream–downstream gradient in this watershed.     

Effects of fish age versus size on the development of whirling disease in rainbow trout

We examined the effects of both fish age and size on the development of resistance to whirling disease in Erwin strain rainbow trout. Previously, we demonstrated that juvenile rainbow trout became resistant to development of the disease when first exposed to triactinomyxons of the parasite Myxobolus cerebralis at about 9 wk post-hatch when raised at 12 degrees C, but ages and sizes of fish used in that experiment were confounded (Ryce EKN, Zale AV, MacConnell E [2004] Dis Aquat Org 59:225-233). In this study, rainbow trout of the same age and different sizes, and the same size and different ages, were exposed to the parasite to distinguish the influences of age and size. Fish were reared at 3 different water temperatures prior to exposure to produce groups with different growth rates and were exposed to the parasite at 7 or 9 wk post-hatch. Disease severity was affected by both age and size at first exposure, but the effects were not independent. An increase in fork length from 36 to 40 mm among fish exposed at 7 wk post-hatch did not confer increased resistance, but the same increase in size at 9 wk post-hatch did. Similarly, an increase in age from 7 to 9 wk post-hatch among fish exposed at 36 mm fork length did not confer increased resistance, but the same increase in age at 40 mm did. Rainbow trout must be both 9 wk post-hatch or older and at least 40 mm in fork length at time of exposure to exhibit enhanced resistance to whirling disease. Resistance to disease was not associated with the level of skeletal ossification.     

Age and growth of Lutjanus kasmira (Forskål) in Hawaiian waters

The growth of Hawaiian taape, Lutjanus kasmira , was studied by examining otoliths and by analysing length-frequency distribution. Annual hyaline and opaque markings were visible in whole mounts of sagittae, which were verified by enumeration of daily increments with a scanning electron microscope (SEM) and through marginal increment analysis. The von Bertalanffy growth curve was fitted to the data, resulting in: where t. l . is total length (cm) and t is age (years). SEM observations revealed that the slowgrowth hyaline zones were composed of daily increments too small (0.4–0.8 μm) to be resolved optically. Thus, age estimates derived by numerically integrating otolith growth rate data obtained with a light microscope showed a negative bias, resulting in overestimation of growth rates. Parameter estimates obtained from three different types of length-frequency analysis were also unstable. This was due, at least in part, to differences in the size composition of fish sampled with different fishing gears and from different depths.
The growth rate registered in Hawaii falls within the reported growth coefficients of lutjanids, whereas it is one of the highest in the Pacific and clearly higher than a deep-water lutjanid species growth in Hawaii. Probably, this high growth rate may have been enhanced by the relative lack of competitors in the depauperate Hawaiian marine fish community.     

Age determination,growth and mortality of Gerres subfasciatus Cuvier, 1830 in southeast Australia

Commercial beach‐seine (30–50 mm cod‐end mesh) catches of Gerres subfasciatus in Lake Macquarie southeast Australia were sampled monthly between December 2000 and April 2002 to investigate species age, growth and mortality characteristics using sectioned sagittal otoliths. Inclusion of fishery‐independent length data of young‐of‐the year collected from littoral seagrass beds with fine meshed beach seines augmented growth analyses. Fifty otoliths each month (total 448 female and 402 male) were examined with sections displaying alternating opaque and translucent zonation. Formation of otolith opaque zones occurred annually between August and December as determined by monthly marginal increment analyses. Spawning occurred between October and February, and a universal birth date of 1 December was assigned that allowed counts of opaque zones to be converted to age estimates in years and months (decimal ages). The von Bertalanffy growth function identified that both genders grew fast for their initial 2 years, but thereafter slowed. Females grew faster, had a greater mean fork length‐at‐age, estimated L_∞ and an observed greater maximum fork length in samples compared to males. Nevertheless, observed longevity was 10⁺ years for both genders. Commercial catches of both genders were dominated by the 2⁺ and 3⁺ year age classes. Catch curve analyses identified the instantaneous rate of total annual mortality to be ~0.8 and an exploitation rate of <0.5 for both genders. The data form a basis for developing assessment and management strategies of G. subfasciatus fisheries.     

Age determination and growth of the pollan, Coregonus autumnalis pollan Thompson, of Lough Neagh, Northern Ireland

Scales from Lough Neagh pollan display a large number of checks, making age determination difficult. Sclerite counts showed that an annual check is formed on scales in May and a second accessory check in most young fish in October. The method of ageing from scales was supported by inspection of length-frequency plots and by following the growth of pollan in their first 2 years of life. The body-scale relationship was curvilinear. Back-calculation showed that pollan of both sexes attain a fork length of 29 cm in 5 years (1 ∞=28.9 cm; k = 0.65; l ₀= -0.06 year). There is no evidence that annual growth rates have changed since 1965. Possible environmental causes of scale check formation are discussed.     

Direct ageing of Thunnus thynnus from the eastern Atlantic Ocean and western Mediterranean Sea using dorsal fin spines

This study deals with important methodology issues that affect age estimates of eastern Atlantic bluefin tuna Thunnus thynnus using dorsal fin spines. Nearly 3800 spine sections were used from fish caught in the north‐east Atlantic Ocean and western Mediterranean Sea over a 21 year period. Edge type and marginal increment analyses indicated a yearly periodicity of annulus formation with the translucent bands (50% of occurrence) appearing from October to May. Nucleus vascularization seriously affected specimens older than 6 years, with the disappearance of 40–50% of the presumed annuli by that age. An alternate sectioning location was a clear improvement and this finding is an important contribution to the methodology of using this structure for ageing the full‐length range of eastern T. thynnus. Finally, there were no significant differences between the coefficients of von Bertalanffy growth model estimated from mean length at age data (L_∞ = 327·4; k = 0·097; t₀ = ?0·838) and those estimated from the growth curves accepted for the eastern and western T. thynnus management units.     

水丰水库的池沼公鱼生物学

本文报道了1942年横断鸭绿江而成的水丰水库的池沼公鱼生物学,内容包括性状变异、年龄和生长、食性、繁殖、群体结构、群体消长变化及渔业利用。水丰水库的池沼公鱼一龄体长(到尾叉的体长,后同)74毫米,体重3克;二龄体长99毫米,体重6.5克。体长体重关系式:logW=2.5306logL-1.7590。主要以浮游动物为食,但不同栖息地点食物组成有明显差异。一龄即达性成熟;性比为1♀:1.24♂;个体繁殖力905—19051粒,平均4330粒;个体繁殖力Y(百粒鱼卵)与体长L(厘米)的相关方程式为Y=58.4860L-402.7606;群体增殖速度(Vp)等于1494;4至5月在水库岸边产卵,卵粘性,水温10—15℃,约经12天孵出仔鱼。群体由1—3龄3个龄组组成,1321尾标本的平均年龄为1.15;65.1—80毫米体长组的个体为主要渔获对象,占整个渔获的65.5%。池沼公鱼是目前水丰水库第一位的经济鱼类,1982年鱼产量120万斤,占总鱼产的57.8%。       

Comparison of otolith growth and morphology with somatic growth and age in young-of-the-year bluefin tuna

Otolith morphological characteristics were studied using image analysis techniques and the relationships between otolith growth and somatic growth and age, as estimated from counting daily otolith increments, were examined in young-of-the-year (YOY) bluefin tuna Thunnus thynnus ranging in fork length ( L _F) from 8·5 to 55·5 cm. Whole otolith length, width, area and perimeter, and three shape indexes, circularity, E value and rectangularity, were extracted for each pair of sagittae. Since no statistical significant differences between left and right otolith morphometrics were found, only one otolith from each fish was used for correlations. Statistically significant relationships were observed between otoliths measurements and fish somatic growth when a linear regression was applied after logarithmic transformation of all variables tested. Among the variables, otolith length was the one that showed the highest correlation with L _F, followed by otolith area and perimeter, whereas otolith rectangularity exhibited the lowest correlation. Statistically significant relationships were also observed between the otolith variables tested and the age of the fish, which ranged from 20 to 129 days. The ages estimated using otolith mass were very close to those assessed using daily increment counts (bias ranged from 1 to 24 days). Therefore, otolith mass could represent a valuable criterion for age estimation in YOY bluefin tuna that is objective, economic and easy to perform compared to daily increment counting method.     

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.