Age and growth of blue grenadier, Macruronus novaezelandiae (Hector), in south-eastern Australian waters

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.

2017 ◽  
Vol 98 (5) ◽  
pp. 1197-1203 ◽  
Author(s):  
Pablo Denuncio ◽  
María Fernanda Negri ◽  
Ricardo Bastida ◽  
Diego Rodríguez

Knowledge of growth patterns of an animal species is fundamental to understand their life history. This information is also used to help define population boundaries of threatened cetaceans, such as the Franciscana dolphin, Pontoporia blainvillei. A total of 108 Franciscana dolphins incidentally captured in artisanal fishing nets in estuarine and marine coastal waters of the northern part of the Franciscana Management Area IV (North FMA IV), Argentina, were studied. The objective of the present paper was to study age and growth parameters of Franciscanas from North FMA IV and to compare these parameters between estuarine and marine potential populations within this area. We used von Bertalanffy and Gompertz growth curves to model growth trajectories. The estimated asymptotic lengths demonstrated that Franciscana dolphins from this area were smaller (females: 136.3 cm and males, 122.1 cm) than southern FMA IV values previously published. They also showed the reverse sexual size dimorphism that is known across their range. However, the estimated asymptotic length was not statistically different between the estuarine and marine females within the study area. In spite of this, the fact that the northern forms of the FMA IV were smaller than the southern specimens supports the hypothesis of more than one population of the species within this management area. The North FMA IV has the highest reported mortality levels of Franciscana dolphins within the FMA IV; these results are relevant to the knowledge base of Franciscana dolphins in the region.


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.


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.


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.


2018 ◽  
Vol 16 (1) ◽  
Author(s):  
Marília Hauser ◽  
Carolina R. C. Doria ◽  
Larissa R. C. Melo ◽  
Ariel R. Santos ◽  
Daiana M. Ayala ◽  
...  

ABSTRACT The goliath catfish Brachyplatystoma rousseauxii has crucial economical and ecological functions in the Amazon basin. Although its life history characteristics have been studied in the Amazon, there is little information in the Madeira River basin, which holds genetically distinct populations and where dams were recently built. Using fish collected in Bolivia, Brazil and Peru, this study provides a validation of growth rings deposition and details the growth patterns of B. rousseauxii in the Madeira before the dams’ construction. Age structure and growth parameters were determined from 497 otolith readings. The species exhibits two growth rings per year and sampled fish were between 0 and 16 years old. In the Brazilian portion of the basin, mainly young individuals below 5 years old were found, whereas older fish (> 5 years) were caught only in the Bolivian and Peruvian stretches, indicating that after migrating upstream to reproduce, adults remain in the headwaters of the Madeira River. Comparing with previous publications, B. rousseauxii had a slower growth and 20 cm lower maximum standard length in the Madeira River than in the Amazon River. This study provides a baseline for future evaluation of changes in population dynamics of the species following dams closure.


Author(s):  
Paulo A.S. Costa ◽  
Adriana C. Braga ◽  
Juan P. Rubinich ◽  
Antônio Olinto Ávila-da-Silva ◽  
Cassiano M. Neto

The age and growth of the snowy grouper, Epinephelus niveatus, from central and south-eastern Brazil were studied by otolith analysis from a sample of 341 specimens, ranging from 325 to 1216 mm in total length (TL) caught with bottom longlines between 1996 and 1998. Otolith length grew proportionally with the increasing TL of the fish. Marginal increment analysis indicated that a single opaque band forms each year during autumn–winter. The maximum estimated age was 54 years, which significantly extends the previously estimated life-span of 21–29 years for this species. The von Bertalanffy growth parameters for both sexes were estimated as L∞ = 1098.4 mm TL, K = 0.062 year −1 and t0 = –2.68. The study revealed differences in mean length-at-age and size at recruitment, as well as in growth parameters between the central and the south-eastern Brazilian coast, which can be attributed mainly to different fishing pressures. The snowy grouper was found at depths of 82–492 m, and showed a positive relationship between age and depth, suggesting differential movements of older fish to deeper waters.


1995 ◽  
Vol 46 (8) ◽  
pp. 1127 ◽  
Author(s):  
BM Wolf ◽  
RWG White

Growth of the queen scallop, Equichlamys bifrons, was examined at one site in the D'Entrecasteaux Channel and two sites in the Huon River estuary (Tasmania) by analysing growth rings on the shell and shell hinge ligament, tagging scallops, and using size-frequency techniques. Regular sampling of scallops revealed that shell growth of E. bifrons is seasonal, commencing in late spring and stopping in late autumn. During the remainder of the year, when the water temperature is below ~13�C, shell growth slows or stops and growth rings are formed on the shell and shell hinge ligament. The growth rings on the shell and hinge ligament of E. bifrons were verified as being annual by studying the growth of marked scallops. Long-term growth patterns were similar for E. bifrons from Middleton (D'Entrecasteaux Channel) and from Deep Bay (Huon River estuary). Tagging data collected over the 1992-93 growing season indicated short-term variation in growth between sites. Size-frequency distributions from Middleton and Deep Bay could not be interpreted because smaller scallops were scarce. Smaller size classes were present at Eggs and Bacon Bay (Huon River estuary) and the size-frequency distribution was resolved into age classes. Reasonable agreement was found between the von Bertalanffy growth parameters obtained from the size frequency, tagging, and growth ring data.


Author(s):  
P. Battaglia ◽  
A. Potoschi ◽  
M. Valastro ◽  
F. Andaloro ◽  
T. Romeo

This paper provides for the first time data on age and growth ofRemora osteochir, also describing its sagittal otolith together with other biological and ecological aspects. Overall, 236 individuals of marlin sucker were collected in the southern-central Mediterranean Sea, from 2008 to 2009. All samples were hosted by the Mediterranean spearfish,Tetrapturus belone, caught by surface longline and harpoon. Analysis of gonads identified a reproductive peak during June and July. The estimated growth parameters according to the von Bertalanffy equation were:L∞= 27.37 cm TL,k= 0.248 year−1,t0= −1.36 year. The length-weight relationship, computed by using eviscerate weight, highlighted an isometric growth for both sexes, as supported by the other results: similar sizes, growth curves and disc length-total length relationship.


2015 ◽  
Vol 96 (5) ◽  
pp. 1157-1166 ◽  
Author(s):  
Rosângela Lessa ◽  
Camila R. Da Silva ◽  
June F. Dias ◽  
Francisco M. Santana

Age and growth of Agassiz's parrotfish Sparisoma frondosum captured off Brazil (Pernambuco) were estimated using sagittal otoliths from 251 specimens. Sex of each specimen was determined and showed that 130 specimens were females (13.1 to 36.8 cm TL) and 121 were males (17.5 to 36.6 cm TL). The otolith marginal increment analysis indicated a single translucent ring formed every year. Parameters of growth curves were derived for the von Bertalanffy (VBGF) and Gompertz models. Based on the Akaike information criterion (AIC), both models were suitable for describing the growth of this species. VBGF parameters were estimated for males L∞ = 39.74 cm TL, K = 0.22, t0 = −1.63 years, females L∞ = 32.38 cm TL, K = 0.44; t0 = −0.23 years; and for the sexes combined L∞ = 33.66 cm TL, K = 0.41, t0 = −0.27 years. The study showed that 55% of individuals were 3 and 4 years of age, with maximal age of 9 years. Mature females (>17.6 cm TL) accounted for 45% of the sample. The age at first maturity for females was 1.6 years. For males the size at first maturity was not determined as immature individuals were not present in the overall sample. Also, primary males (PM) and specimens with gonads undergoing sexual transition were not found. The age structure and growth parameters for S. frondosum are an important contribution to the assessment of the state of exploitation of this species.


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