scholarly journals Age and growth parameters of the dourado Salminus brasiliensis (Cuvier, 1816) from the river Cuiabá, Mato Grosso State, Brazil

2016 ◽  
Vol 38 (1) ◽  
pp. 59 ◽  
Author(s):  
Marina Soares Zuliani ◽  
Angela Maria Ambrosio ◽  
Talitha Mayumi Francisco ◽  
Thiago José Balbi ◽  
Edson Kiyoshi Okada ◽  
...  
2014 ◽  
Vol 104 (4) ◽  
pp. 413-417 ◽  
Author(s):  
Angela M. Ambrosio ◽  
Thiago J. Balbi ◽  
Talitha M. Francisco ◽  
Luiz C. Gomes ◽  
Marina S. Zuliani ◽  
...  

This study has aims to determine the age and to estimate the growth parameters using scales of the species. Individuals of Piaractus mesopotamicus (Holmberg, 1887) used in this study were captured in the commercial fishery conducted in the region, along the year 2006. The model selected to express the growth of the species was the von Bertalanffy Sl= Sl∞*[1-exp-k(t-to)]. To determine if scales are suitable for studying the growth of pacu, we analyzed the relation between standard length (Sl) and the radius of the scales through linear regression. The period of annuli formation was determined analyzing the variations in the marginal increment and evaluating the consistency of the readings through the analysis of the coefficient of variations (CVs) for the average standard lengths of each age (number of rings) observed in the scales. The relationship between Ls of the fish and the radius of the scales showed that scales can be used to study the age and growth of P. mesopotamicus (R= 0.79). CVs were always below 20%, demonstrating the consistency of the readings. Annuli formation occurred in February, probably related to trophic migration that occurs in this month in the region. Equations that represents the growth in length obtained for P. mesopotamicus are Sl=50.00*[1-exp-0.18(t-(-3.00)] for males and Sl=59.23*[1-exp-0.14(t-(-3.36)] for females. The growth parameters obtained in this study were lower compared to other studies previously conducted for the same species and can related to overexploitation that species is submitted by fishing in the region. These values show also that females of pacu attain greater asymptotic length than males that growth faster.


2009 ◽  
Vol 60 (5) ◽  
pp. 394 ◽  
Author(s):  
Francisco Cerna ◽  
Roberto Licandeo

The shortfin mako, Isurus oxyrinchus, is a large pelagic shark with a widespread global distribution. However, very little is known about most aspects of this species for the south-eastern Pacific. In the present paper, the age and growth parameters of the shortfin mako, caught by Chilean swordfish longline fisheries from 2004 to 2005, are reported. Ages were estimated by counting band-pairs from sections of vertebral centra from 547 individuals, ranging from 76 to 330 cm in total length (TL). Trends in the proportion of opaque edges for all ages combined and grouped into ages 0–6 and 7–26 years indicated that they are formed during summer and showed that annually, one band-pair is formed in the vertebrae of shortfin makos. Modal-progression analysis was used to verify the first three age classes (ages 0–2 years). For both sexes, the oldest estimated age was 25+ years. Von Bertalanffy growth parameters were estimated at L∞ = 325.29 cm TL, K = 0.076 year–1 and t0 = –3.18 years for females and L∞ = 296.60 cm TL, K = 0.087 year–1 and t0 = –3.58 years for males. The results indicated that this species is highly vulnerable to exploitation and, thus, urgent conservation measures are required.


2009 ◽  
Vol 57 (4) ◽  
pp. 273-285 ◽  
Author(s):  
Marcelo Francisco de Nóbrega ◽  
Rosangela Paula Lessa

Age and growth of the king mackerel (Scomberomorus cavalla) were estimated for northeastern Brazil. A total of 405 sagittal otoliths from 140 males (24.4-112 cm), 73 females (28-114.8 cm) and 193 specimens of unknown sex (11.5-121 cm) were examined. Marginal increment analysis indicated an annual pattern for growth band deposition. The age classes ranged from 1 to 15 years. Length ranged from 11.5 to 121 cm. The Schnute model indicated that the von Bertalanffy growth model demonstrated the best adjustment, with p=1/b, and was therefore used for estimating growth. Back-calculated curves had smaller variances, giving the following estimated growth parameters for males: L∞= 116.8 cm, K = 0.190, t0 = 0.377; and females: L∞= 132.7 cm, K = 0.159 and t0 = 0.387. In order to compare the curves for males and females, the overlapping of 95% confidence intervals was performed for the parameters generated from the von Bertalanffy non-linear least square method. Specimens between 3 and 8 years of age represented 82.2% (n=5,783) of the catch composition, characterizing the species as a catchable stock in the region.


2017 ◽  
Vol 15 (1) ◽  
Author(s):  
Rosa S. Santos ◽  
Marcus R. da Costa ◽  
Francisco G. Araújo

ABSTRACT Studies on age and growth of fish populations have direct application in fisheries and contribute for policies of conservation. Our aim was update information on the Micropogonias furnieri growth parameters based on sagittae otoliths annulis readings, and we expected that the studied population from Southeast Brazil can reach more longevity than the reported in the available literature. We examined 286 individuals between August-2010 and July-2011 from Ubatuba Bay, SP. The Total Length ranged 200-480 mm. The determined growth parameters were: Males, L∞ =523.4mm, k = 0.05×year-1, t0 = -8.78 year; Females L∞ = 573.5mm, k = 0.06 × year-1, t0 = -7.49 year. The MI and % of edge type evidenced the formation of one ring per year during autumn/winter, coinciding with low temperature and low growth rate. These results differed from those reported for the Vazzoler’s Population I (summer), and we detected higher longevity (45-48 years) as compared with the recorded in the available information.


2018 ◽  
Vol 59 (1) ◽  
pp. 97-110 ◽  
Author(s):  
Mado Kotsiri ◽  
Ioannis E. Batjakas

The otoliths of the Atlantic bonito, Sarda sarda (Bloch, 1793), were examined with the aim to estimate the age and growth of the species in the eastern Mediterranean Sea and to reveal possible relationships between otolith shape or size and age. All specimens used in this study, ranging from 7.2 to 70.4 cm in fork length and from 20 to 4889 g in total weight, were caught in the Aegean and Ionian Seas during the period 1997-2010. Otolith morphometry was studied using image analysis techniques for all intact sagittae ranging in weight from 0.6 to 11.3 mg and four shape indices were calculated. No statistical significant differences between left and right otolith morphometric variables were found. The age of fish was estimated by counting the pairs of opaque and translucent bands in transversal thin sections of otoliths. The estimated ages ranged from 0+ to 7 years and the von Bertalanffy growth parameters were determined \((L∞=79.9 cm, k=0.261 and to=-1.230 years)\). The examination of the type of growth bands at the outside margin of each otolith per month showed that one translucent band is formed annually during the cold season. The results revealed statistically significant relationships between otolith morphometric variables and fish length or age. Among the variables, otolith weight was the one that showed the highest correlation with age (R=0.77). Therefore, otolith weight could represent a valuable criterion for age estimation in Atlantic bonito that is objective, economic and easy to perform compared to annuli counting method in hard parts.


1989 ◽  
Vol 40 (2) ◽  
pp. 215 ◽  
Author(s):  
AF Withell ◽  
JWJ Wankowski

Age and growth were estimated from counts of otolith annuli for pink ling (Genypterus blacodes) and gemfish (Rexea solandri). Sections of otoliths were preferable for age determinations of pink ling, whereas whole otoliths were preferable for gemfish. Validation of the assigned age classes was not achieved. Petersen's length-frequency method was unsuccessful and marginal increment methods were unsuitable for the species studied. Growth of males and females did not differ significantly for either pink ling or gemfish. Both species had a relatively slow growth rate, had a moderately long life-span and could reach body lengths in excess of 1 m. Maximum ages of pink ling and gemfish were, respectively, 21 and 13 years. Mean length-at-age and the von Bertalanffy growth functions were estimated. For pink ling (all individuals combined), K = 0.095 and L∞ = 135.5 cm. For gemfish the best estimates were K = 0.153 and L∞ = 112.3 cm. Precision of age determinations made independently by two readers for pink ling and gemfish, respectively, was 65% and 95% within �1 annulus; average per cent error, respectively, was 4.7% and 3.1%. Paired t-tests on ages assigned to each species by the two readers indicated no significant difference between ages assigned to gemfish, but there was a significant, albeit unbiased, difference for ages assigned to pink ling. However, for pink ling, estimates of the growth parameters derived separately from age determinations by the two readers were virtually identical.


KSTU News ◽  
2021 ◽  
pp. 11-25
Author(s):  
Beraki Weldegiorgish Teklekhaimanot ◽  
Sergey Vadimovich Shibaev ◽  
Sergey Yurievich Gulyugin

In this study, 292 blue sharks Prionace glauca (Linnaeus, 1758) (from 151 to 305 cm total length, TL) were collected off western Africa in the eastern central Atlantic Ocean between 1980 and 1982. Vertebral sections of females specimens ranged from 175 to 300 cm and males specimens ranged from 166 to 312 cm TL were processed and analyzed for age and growth parameters. Growth band pairs (translucent and opaque bands) were counted on the images photographed from the stained whole vertebrae using digital microscope called Digi Scope II. The band pairs after the birthmark were counted from 3 to 12 for males and from 4 to 13 for females. Growth parameters were derived using the Von Bertalanffy growth function (VBGF) based on FISAT and solver solution Microsoft excel and Ford Wall-Ford. VBGF was that which best fit the data. Parameters derived from the combination of observed and back-calculated lengths, K = 0.1, L_∞ = 386.4 cm and t_0 = −1.35 year for males and K = 0.12 year -1, L_∞= 355 cm and t_0 = –1.02 year for females were considered to best describe growth. The longevity was estimated to be at least 23.7 and 28.3 years for females and males respectively. The natural mortality rate was estimated to be 0.15 year - 1 and 0.18 year -1 for males and females respectively.


1987 ◽  
Vol 38 (5) ◽  
pp. 625 ◽  
Author(s):  
TJ Kenchington ◽  
O Augustine

Blue grenadier, Macruronus novaezelandiae, from south-eastern Australian waters were aged, using their otoliths (whole and in transverse thin sections). The greatest recorded age was 25 years. A double blind test showed that the recorded ages were sufficiently reproducible to use in fitting growth curves (Index of Average Percent Error: 8%), but not sufficiently so to assign individuals to particular year-classes. Von Bertalanffy growth curves were fitted to both length and weight data. For males, Lt = 90.7 (1 - exp[-0.256(t + 1.21)]} and Wt = 2.62 (1 - exp[-0.277(t + 1.39)]}3. For females, Lt = 99.3 {l - exp[-0.203(t + 1.48)]} and Wt = 4.16{1 - exp[-0.157(t + 2.93)]}3. L is the length in centimetres, W is the weight in kilograms and t is the age in years. A comparison with length-frequency modes validated the growth curves for immature fish, but no validation was possible for the adults. The $exes have qignificantly different growth patterns. Their growth parameters are typical of those of commercially exploited, temperate gadoid fishes and show no modification for the deep-water zone inhabited by blue grenadier.


2020 ◽  
Vol 98 (7) ◽  
pp. 481-494
Author(s):  
M.C. Risoli ◽  
A. Baldoni ◽  
J. Giménez ◽  
B.J. Lomovasky

Morphometric relationships and age and growth rates of the yellow clam (Mesodesma mactroides Reeve, 1854 = Amarilladesma mactroides (Reeve, 1854)) were compared in two populations from Argentina: Santa Teresita (36°32′00″S) and Mar del Plata (37°57′52″S). The Santa Teresita clams were heavier (shell, soft parts) than the Mar del Plata clams. Cross sections stained with Mutvei’s solution and acetate peels revealed an internal shell growth pattern of well-defined slow-growing translucent bands and alternating fast-growing opaque bands. Translucent bands (clusters) representing external rings were formed mostly during October in both sites, coinciding with gonadal maturation processes and spawning. Data confirm the annual formation of translucent bands in this species. Comparison of growth parameters showed a higher growth rate k and lower maximum age in Mar del Plata (8 years) than in Santa Teresita (9 years), which could be triggered by differences in salinity between localities due to the influence of the Rio de la Plata estuary, which is strongly linked to climate variability. Shell mass condition index and Oceanic Niño Index were negatively correlated, showing the influence of El Niño in shell properties of the species. Considering that events are becoming more intense and frequent, changes in growth rates and shell properties of Santa Teresita’s population could be expected to be more vulnerable under climate change.


1992 ◽  
Vol 43 (5) ◽  
pp. 983 ◽  
Author(s):  
JR Anderson ◽  
AK Morison ◽  
DJ Ray

Transverse thin sections (0.5 mm thick) of sagittal otoliths from 290 Murray cod up to 1400 mm in total length and 47.3 kg in weight were used to establish the age and growth of cod in the lower Murray-Darling Basin, including comparisons of recent (1986-91) and past (1949-51) growth rates and growth in different waters. The maximum estimated age was 48 years. Quantitative and qualitative analysis of the seasonal changes in otolith marginal increments showed that annuli in fish of all ages were laid down each spring, and 1 October was assigned as the birthday. The thin-sectioning method was validated by comparing age estimates for 55 Murray cod from Lake Charlegrark (age 0-21 years), which had been validated by using burnt and polished half-otoliths. The new method had an accuracy of 96.4% and it offers major advantages in ease of preparation, reading, and batch-handling of large numbers of otoliths. The precision of the method, estimated as an average error for four readers, was 5.4% (3.0% after ignoring discrepancies in relation to annuli on otolith edges). There was a linear relationship between otolith weight and fish age and an exponential relationship between otolith weight and fish length. Both otolith length and otolith width reached an asymptote at about 15 years, when fish length also approached its maximum. However, otolith thickness continued to increase throughout the life of the fish and, after about 15 years, contributed most to the increase in otolith weight. This confirmed that otoliths continued to grow in thickness and that annuli were laid down throughout life, and that cod could be aged reliably to the maximum age. The annulus pattern is very clear and distinct, and the reading techniques are fully described, including recognition of 'larval' and 'false' rings. Various differences were found in the growth rates, and the length-weight relationships for males and females, for cod caught in 1986-91 and those caught in 1949-51, and various subpopulations are discussed. The von Bertalanffy growth parameters (all individuals combined) were estimated at L∞ = 1202 mm, k=0.108 and t0= -0.832. The availability of a reliable ageing method provides the first opportunity to determine year of birth and thus to examine the age structure of populations and to effectively manage cod populations that have declined in abundance.


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