Age and growth of Murray Cod, Maccullochella peelii (Perciformes: Percichthyidae), in the Lower Murray-Darling Basin, Australia, from thin-sectioned Otoliths

1992 ◽  
Vol 43 (5) ◽  
pp. 983 ◽  
Author(s):  
JR Anderson ◽  
AK Morison ◽  
DJ Ray
Keyword(s):  
Growth Rates ◽  
Growth Parameters ◽  
Age And Growth ◽  
Average Error ◽  
Fish Length ◽  
Exponential Relationship ◽  
Thin Sections ◽  
False Rings ◽  
Murray Darling Basin ◽  
Murray Cod

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.

scholarly journals Starost, rast i morfometrija otolita palamide (Sarda sarda Block, 1793) iz istočnog Sredozemnog mora

2018 ◽  
Vol 59 (1) ◽  
pp. 97-110 ◽  
Author(s):  
Mado Kotsiri ◽  
Ioannis E. Batjakas
Keyword(s):  
Growth Parameters ◽  
Eastern Mediterranean ◽  
Fork Length ◽  
Cold Season ◽  
Age And Growth ◽  
Fish Length ◽  
Thin Sections ◽  
Significant Relationships ◽  
The One ◽  
Sarda Sarda

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.

Validation of the use of thin-sectioned Otoliths for determining the age and growth of Golden Perch, Macquaria ambigua (Perciformes: Percichthyidae), in the Lower Murray-Darling Basin, Australia

1992 ◽  
Vol 43 (5) ◽  
pp. 1103 ◽  
Author(s):  
JR Anderson ◽  
AK Morison ◽  
DJ Ray
Keyword(s):  
Growth Rates ◽  
Total Weight ◽  
Birth Date ◽  
Fish Length ◽  
Thin Sections ◽  
Continuous Growth ◽  
Total Length ◽  
Murray Darling Basin ◽  
The Mean ◽  
Age Estimates

Golden perch, Macquaria ambigua, from the Murray-Darling Basin were aged by using transverse thin sections of their sagittal otoliths. Samples from 889 fish were obtained from riverine and lacustrine habitats and from wild and stocked populations. Error in the precision of age estimates (calculated as the mean percentage error of the independent age estimates of four readers) was 5.6% (3.9% after allowing for discrepancies in relation to the annual mark on the edge of the otolith). Validation was accomplished by using a combination of analysis of the progression of modes in length-frequency distributions, qualitative and quantitative marginal-increment analysis, and analysis of age estimates of fish from populations with a known stocking history. The technique was validated for fish up to 8 years of age (455-545 mm total length, 1695-3988 g total weight), and the greatest recorded age was 16 years (530-600 mm total length, 2607-4050 g total weight). Annual marks become visible in otolith sections in most fish of all ages in October, and 1 October was designated as the birth date. A description of our method of reading sections of golden perch otoliths, including recognition of false annual marks, is given. Otolith length, width and thickness increased linearly with fish length and with loglo(fish age), whereas otolith weight increased linearly with fish age and exponentially with fish length. The continuous growth of the otoliths and the consistency in the appearance of annual marks support the accuracy of estimates up to the maximum recorded age. The mean length-at-age and the parameters of the length-weight relationship were estimated. The von Bertalanffy growth parameters were also estimated (L∞ =507 mm, to=0.420 years, K=0.454). No significant differences were found in growth rates or length-weight relationships between males and females. However, growth (particularly in weight) was highly variable among sites and years, and slow-growing 5-year-olds may be shorter than fastgrowing 1-year-olds. Ages were estimated for a sample of 86 golden perch caught between 1949 and 1951 but a comparison of growth rates between these and more recent collections was inconclusive.

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
Keyword(s):  
Growth Parameters ◽  
Growth Curves ◽  
Growth Patterns ◽  
Age And Growth ◽  
Double Blind ◽  
Blind Test ◽  
Thin Sections ◽  
South Eastern ◽  
Weight Data ◽  
Immature Fish

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.

scholarly journals Age and growth variability of the yellow clam (Mesodesma mactroides) in two populations from Argentina: implications under climate change

2020 ◽  
Vol 98 (7) ◽  
pp. 481-494
Author(s):  
M.C. Risoli ◽  
A. Baldoni ◽  
J. Giménez ◽  
B.J. Lomovasky
Keyword(s):  
Climate Change ◽  
Cross Sections ◽  
Growth Rates ◽  
Growth Parameters ◽  
Shell Growth ◽  
Condition Index ◽  
Age And Growth ◽  
Shell Mass ◽  
Growth Variability ◽  
Two Populations

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.

Age, growth and mortality of redfish Centroberyx affinis

2001 ◽  
Vol 52 (4) ◽  
pp. 637 ◽  
Author(s):  
A. K. Morison ◽  
K. R. Rowling
Keyword(s):  
Growth Rate ◽  
Significant Variation ◽  
Fork Length ◽  
Age And Growth ◽  
Average Error ◽  
Natural Mortality ◽  
Commercial Catch ◽  
Thin Sections ◽  
The Mean ◽  
Age Estimates

Age and growth of 5678 redfish, collected during 1991–98 from Australia’s South East Fishery, were estimated from thin sections of otoliths. A maximum age of 44 years was recorded for a 30 cm (fork length) female, but 80%of females in the commercial catch were <10 years, and 80%of males were <13 years. The largest was a 34 cm female estimated to be 36 years old. Repeated age estimates of a subsample revealed an average error of 3.79%. There was significant variation in the mean length-at-age among years, and there were significant effects for age*year, age*sex, age*region, region*year, and sex*region*year interactions. Assessments of the fishery have assumed a single stock, because tagging results from the 1980s indicate movement of redfish along the coast. This study found consistent differences in sex ratio and growth rate between regions, which indicate some structuring within the population. However, the differences in growth rates are not consistent among years and could not be explained by differences in depths fished, suggesting a more dynamic situation than spatially segregated stocks. Estimates of natural mortality ranged from 0.07 to 0.11 year–1 and differed between regions.

Growth rates of four Hawaiian deep slope fishes: a comparison of methods for estimating age and growth from otolith microincrement widths

1997 ◽  
Vol 54 (1) ◽  
pp. 126-136 ◽  
Author(s):  
H A Williams ◽  
M K Lowe
Keyword(s):  
Growth Rates ◽  
Growth Curves ◽  
Age And Growth ◽  
Interval Length ◽  
Fish Length ◽  
Comparison Of Methods ◽  
Increment Width ◽  
Daily Increment ◽  
Minimum Number ◽  
Age Estimates

Two methods were used to estimate the age and growth of four Hawaiian deep slope fishes. Otolith daily increment width estimates from radial sections of sagittal otoliths were integrated over the otolith radius to approximate age by (i) dividing interval length (micrometres) by mean increment width (micrometres per day) and summing this quotient for consecutive 500- µm radial intervals (S. Ralston and H.A. Williams. 1989. Fish. Bull. 87: 1-16) and (ii) fitting increment width (y) versus otolith radius (x) to a Gompertz rate curve and calculating the inverse integral of this curve (M.K. Smith and E. Kostlan. 1991. Fish. Bull. 89: 461-472). The methods also differ in the way the age-length key is generated. Ralston and Williams' method uses integrated age versus a regression-based estimate of fish length at 500- µm otolith radial intervals; Smith and Kostlan's method uses estimated age versus actual fish length. Neither method of integration produced significantly different age estimates; however, the use of regression-based fish length estimates instead of sampled fish lengths resulted in significant differences between estimated growth curves. The minimum number of daily increment width estimates required as a function of otolith radius was calculated, on the basis of observed microincrement width variation.

Validation of the use of Otoliths to determine the ate and growth of Murray Cod, Maccullochella peelii (Mitchell) (Percichthyidae), in Lake Charlegrark, Western Victoria

1992 ◽  
Vol 43 (5) ◽  
pp. 1091 ◽  
Author(s):  
GJ Gooley
Keyword(s):  
Sex Difference ◽  
Growth Parameters ◽  
Sampling Period ◽  
Age And Growth ◽  
Birth Date ◽  
Beach Seine ◽  
Growth Ratio ◽  
Gill Net ◽  
Murray Cod ◽  
Western Victoria

The age and growth of Murray cod, Maccullochella peelii, in Lake Charlegrark, western Victoria, were determined by using otoliths from fish sampled by beach-seine and gill-net, or caught by anglers, between August 1978 and August 1982. Annulus formation was validated up to 11 + years by several methods. Otoliths were examined from hatchery-bred fish of known age (up to 4+ years) that had been stocked into local farm ponds. Analysis of incremental growth for all fish sampled from the lake indicated that the mean edge-growth ratio was lowest, and the percentage of otoliths with an annulus at the edge was highest, in October. A nominal birth date of 1 October was designated for the population to enable calculation of the absolute age for each fish. Age-composition data for those fish taken by gill-net and by anglers (up to 21 + years) revealed modal progression of strong year classes (1970 to 1973 inclusive) during the sampling period. Length-frequency data for those fish taken by beach-seine (up to 3 + years) revealed modal progression, on a seasonal basis, of two relatively strong year classes (1978 and 1979) during the sampling period. A von Bertalanffy growth curve was fitted to length and age data for all fish collected in the lake (no sex difference, P>O.05), and growth parameters were estimated for the population (L∞ = 695 mm). This curve did not adequately describe the growth of fish older than 11 + years because the majority of sampled fish (98.3%) were aged 11 + years or younger. The length-weight relationship for the population was determined by using data from all fish collected in the lake (no sex difference, P>0.05).

scholarly journals Interannual variability in size structure, age, and growth of jumbo squid (Dosidicus gigas) assessed by modal progression analysis

2010 ◽  
Vol 68 (3) ◽  
pp. 507-518 ◽  
Author(s):  
Friedemann Keyl ◽  
Juan Argüelles ◽  
Ricardo Tafur
Keyword(s):  
Interannual Variability ◽  
Growth Rates ◽  
Size Structure ◽  
Growth Parameters ◽  
Maximum Size ◽  
Age And Growth ◽  
Dosidicus Gigas ◽  
Jumbo Squid ◽  
Observation Bias ◽  
Slow Growing

Abstract Keyl, F., Argüelles, J., and Tafur, R. 2011. Interannual variability in size structure, age, and growth of jumbo squid (Dosidicus gigas) assessed by modal progression analysis. – ICES Journal of Marine Science, 68: . A range of growth rates, longevity, maximum size, and number of annual cohorts have been documented for jumbo squid (Dosidicus gigas). Genetic and phenotypic plasticity have been mentioned as possible sources of the differences in maximum sizes. Here, a large dataset on length frequencies derived from the industrial jig fishery for the species off Peru from 1991 to 2007 was corrected for observation bias introduced by the fishing gear and used to analyse growth-related parameters by modal progression analysis (MPA). Mean growth rates of 33 cohorts varied interannually (11–44 mm month−1), as did longevity (11.1–32.1 months) and mean maximum size (273–1024 mm). Intra-annual difference in growth parameters was not significant. The number of cohorts per year fluctuated between 0 and 6. Fast-growing cohorts with medium longevity and large terminal size were found during moderately cool periods, and long-lived, slow-growing cohorts with small terminal size during extreme ecosystem conditions (El Niño and La Niña). The application of MPA to cephalopod populations has been rejected before, but the results presented suggest that a modified approach is appropriate if it allows for varying growth parameters and includes a correction for observation bias.

Variable growth band deposition leads to age and growth uncertainty in the western wobbegong shark, Orectolobus hutchinsi

2007 ◽  
Vol 58 (9) ◽  
pp. 856 ◽  
Author(s):  
Justin A. Chidlow ◽  
Colin A. Simpfendorfer ◽  
Garry R. Russ
Keyword(s):  
Growth Rates ◽  
Growth Parameters ◽  
Somatic Growth ◽  
Age And Growth ◽  
Age Validation ◽  
Band Formation ◽  
Growth Band ◽  
Total Length ◽  
In Captivity ◽  
Elasmobranch Species

Age and growth parameters of Orectolobus hutchinsi were estimated using micro-radiographs of sectioned vertebrae from 182 wild caught individuals. Two fluorochrome marker dyes, calcein and oxytetracycline, were used to validate the timing and periodicity of vertebral band formation in nine individuals held in the laboratory for between 423 and 472 days. Growth bands were difficult to interpret and final counts were obtained from only 98 (53.8%) individuals ranging in total length (TL) from 63 to 146 cm. The timing of growth band formation in the vertebrae of captive animals had no predictable temporal pattern, with formation occurring during all seasons of the year, making age validation difficult. Growth band formation was hypothesised to be influenced by non-periodic changes in centrum or somatic growth rather than seasonal growth, as observed in many other elasmobranch species. Growth rates of nine O. hutchinsi held in captivity varied considerably, ranging from 3.5 cm year–1 to 13.8 cm year–1 in total length (mean = 7.03 cm year–1). Although the periodicity of vertebral band formation in captive animals did not support a synchronous annual pattern, captive growth rates matched those predicted when an annual band pattern was assumed for wild caught individuals. Von Bertalanffy growth parameters estimated from vertebral analysis assuming an annual banding pattern and a mean size of birth of 24.1 cm were: L∞ = 149.45 cm and K = 0.117 year–1 for both sexes combined. These results illustrate the fundamental importance of validating the periodicity of growth band formation in elasmobranch age and growth studies as it has considerable implications for the management of fisheries that exploit shark and ray species that may exhibit asynchronous growth band deposition.

Growth and movement of the South African abalone Haliotis midae: A reassessment

1995 ◽  
Vol 46 (3) ◽  
pp. 583 ◽  
Author(s):  
RJQ Tarr
Keyword(s):  
South African ◽  
Growth Rates ◽  
Growth Parameters ◽  
Eastern Coast ◽  
Island Population ◽  
Western Coast ◽  
Eastern Cape ◽  
The South ◽  
Significant Difference ◽  
Haliotis Midae

Growth rates of a number of Haliotis midae populations around the South African coast were studied by means of tagging. These populations ranged from the cool waters of the western coast to the more temperate environment of the eastern Cape. Standard von Bertalanffy growth curves were fitted and growth parameters derived. These ranged from 0.19 to 0.25 for K, the average rate at which L∞ is approached, and from 156 to 173 for L∞, the average theoretical maximum length. These indicate far higher growth rates than were previously published for this commercially fished species, and the reasons for this difference are discussed. The expectation that growth rates would be fastest in the warmer eastern Cape waters was not realized, there being no significant difference in growth between the Bird Island population on the eastern coast and the Robben Island population on the western coast. These new growth parameters indicate that H. midae in the commercial fishery grounds is attaining sexual maturity some four years earlier, and the minimum legal size some five years earlier, than previously considered. This has considerable significance for modelling studies presently underway. Movement of a small population of adult H. midae was studied over a three-year period, after which 47% of the original abalone were still present on the study site. Of these, 81.5% still occupied exactly the same position on the rocks. This indicates that H. midae that have located an optimum habitat, and that are not disturbed, tend not to move.

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