Age and growth of Freshwater Herring, Potamalosa richmondia Macleay (Clupeidae: Hyperlophinae), in the Bellinger River, NSW

1989 ◽  
Vol 40 (6) ◽  
pp. 679 ◽  
Author(s):  
RWJ Pidgeon

The freshwater herring, Potamalosa richmondia Macleay, is a catadromous fish that inhabits coastal rivers of New South Wales. Estimates of the age and growth of this species in the Bellinger River were made from scales. Comparison of scale ages with those from whole otoliths and burnt otolith sections from a sample of 30 fish aged at 2 to 8 years resulted in a 73 and 79% exact agreement and a 97 and 100% agreement within one year, respectively. Marginal-increment analysis of the scales indicated that the annulus was formed during the winter, which is also the spawning season. The ageing method was validated for age classes of 2 to 8 years by these procedures. The age at the first annulus and at ages 9 to 11 years could not be validated. The oldest fish examined was estimated to be 11 years old. The growth rate was very slow in comparison with that of other clupeids. Parameters of the von Bertalanffy growth equation, based on lengths and ages at capture, were L∞ = 252.7 mm, K = 0.126, and t0 = -2.77 years. There was no difference between the sexes in their growth in length. However, the length-weight relationships of males and females were different, with females longer than 180 mm weighing more than males of the same length. The predicted weights at the asymptotic length were 213.2 g for males and 257.6 g for females.

2008 ◽  
Vol 59 (8) ◽  
pp. 684 ◽  
Author(s):  
Gavin L. Butler ◽  
Stuart J. Rowland

Age and growth estimates can be difficult to obtain for endangered fishes owing to their relative low abundance and the ethics associated with sampling threatened populations. The eastern freshwater cod, Maccullochella ikei Rowland 1985, is an endangered freshwater fish endemic to the Clarence and Richmond Rivers of New South Wales, Australia. Bony parts were gathered from archival collections and hatcheries, as well as opportunistically from the wild, to determine age and growth. Examination of opercular bones and dorsal spine sections revealed no consistent annuli. Sectioned otoliths exhibited consistent bipartite rings throughout the structures and 106 otoliths were used to estimate the age of cod from 0+ to 15+ years. Edge increment analysis and known-age cod were used to validate the age estimates. The von Bertalanffy growth equation for M. ikei is Lt = 704.9 (1–exp (–0.20 (t + 0.14))). A length–weight relationship of W = 2.80 × 10–6 × L3.2467 was established from 372 cod collected using non-destructive techniques. Significant differences were found in the relative condition of cod in summer (Kn = 0.999) and winter (Kn = 1.026). The information presented in this paper will assist in the conservation of M. ikei and will provide a guide for future age and growth studies of threatened species.


1995 ◽  
Vol 46 (3) ◽  
pp. 591 ◽  
Author(s):  
FE Wells ◽  
P Mulvay

On the southern coast of Western Australia, proportionately more reproductive specimens of greenlip abalone, H. laevigata, were of legal size in 'good' fishing areas than in 'bad' fishing areas. Sex ratios were usually 1:1. Maturation of the gonads began at a size of 70-90 mm shell length (SL) and by 100-110 mm SL all animals were reproductively mature. Size-specific fecundities were not statistically different among the four good fishing areas examined, nor were they between the two bad fishing areas, but size-specific fecundity was greater in good than in bad fishing areas. Spawning begins as soon as the animals are mature; there is no gap between apparent histological maturity and actual spawning. Gonads are quiescent in the first part of the calendar year. Development is rapid in August and September, when animals begin to reach ripe condition. A maximum proportion of ripe animals occurs in October and November, followed by spawning in December. There was no difference between growth rates of males and females in either the good or the bad fishing areas. The von Bertalanffy growth equation disclosed no difference in growth between good and bad fishing areas, but close inspection of the data suggested that slower growth did occur in the bad fishing areas. The abalone reach reproductive maturity at an age of 2.5 to 3 years and the legal size of 140 mm SL at 5 to 6 years.


Author(s):  
Célia M. Teixeira ◽  
Ana Pinheiro ◽  
Henrique N. Cabral

Sand sole, Solea lascaris, were collected along the Portuguese coast, between October 2002 and July 2003, to examine feeding habits, age and growth and sexual cycle. The most important prey items were Mysidacea, Amphipoda and Polychaeta. Differences in diet according to season and length size were found: Amphipoda were very important in diet during winter, while Echinodermata were consumed mostly in summer; smaller individuals feed on Amphipoda while larger feed on Decapoda. Age of S. lascaris was determined from sagittae otoliths. The length of fish analysed ranged from 61 mm to 340 mm. The von Bertalanffy growth equation parameters differed significantly between sexes (L∞ = 342.3 mm, k = 0.50, t0 = −0.87 and L∞ = 264.5 mm, k = 0.82, t0 = 0.13, females and males, respectively). The highest values of the gonadosomatic index were obtained in winter and spring, when the highest proportion of individuals at spawning stage was recorded.


1980 ◽  
Vol 37 (2) ◽  
pp. 241-247 ◽  
Author(s):  
K. J. Sainsbury

The growth in length of a group of animals is examined. Each animal is assumed to grow according to the von Bertalanffy model with fixed parameters, but these parameters are allowed to differ between individuals. Equations governing the mean and variance of length at given age and growth increment at given length are provided, and their implications discussed. Results indicate that the traditional growth equation is likely to result in an underestimate of the mean value of K when either length at age or growth increment data are analyzed. This problem does not appear serious when using length at age data. However, the problems of interpretation are more serious in the case of growth increment data where serious overestimates of the reconstructed mean length at age can result. A thorough analysis of growth cannot be made for a population exhibiting individual variability in L∞ and K from growth increment data alone. In particular a nonlinear relationship between growth increment and initial length does not necessarily imply that the von Bertalanffy model is inappropriate to the species in question. A topic urgently in need of examination is the form of the joint distribution of K and L∞ in animal populations.Key words: von Bertalanffy, growth models


Author(s):  
Julio Neves de Araujo ◽  
Agnaldo Silva Martins

Coney (Cephalopholis fulva) otoliths were collected from 1997 to 1999 off the central coast of Brazil. Analysis of the edges of otoliths sections suggests that one translucent and one opaque zone are formed once a year. Coney age and size-ranges were 2–25 years and 172–428 mm total length (TL) respectively. The von Bertalanffy growth equation was TLt=316(1−e−0.138(t+5.301)). The maximum age observed in this study is well above that previously reported for coney.


1979 ◽  
Vol 57 (5) ◽  
pp. 1020-1025 ◽  
Author(s):  
Michael C. S. Kingsley

Heavy sea ice in the Canadian Arctic in the winter of 1973–1974 reduced seal populations; polar bears, preying principally on seals, consequently lost weight. The nature and degree of this weight loss was investigated by examining the parameters of von Bertalanffy growth curves, fitted by direct minimization of a sum of squares using the simplex algorithm of Nelder and Mead. Growth rates were lower for both males and females tagged in 1974–1975 than for bears tagged in 1971–1973. Weights of mature bears were unaffected.


Author(s):  
Rui Coelho ◽  
Karim Erzini

Aspects of the population dynamics of the undulate ray, Raja undulata (Chondrichthyes: Rajidae), one of the more abundant elasmobranch fish captured along the Portuguese south coast (Algarve), were studied for the first time. Some traditional elasmobranch vertebral enhancing techniques were compared and the most precise for this species determined to be the cedar wood oil immersion and the alizarin red S stain. The sample consisted of 14 age-classes, with age-classes 3 to 8 being the most represented. Evidence of an annual deposition pattern of a pair of bands (one opaque and one translucent) was found by marginal increment analyses. Von Bertalanffy growth parameters were estimated and no differences found between males and females (all data: Linf=110·22 cm, K=0·11 y−1 and t0=−1·58 y).


2009 ◽  
Vol 7 (4) ◽  
pp. 667-676 ◽  
Author(s):  
Marcelo Francisco de Nóbrega ◽  
Rosangela Paula Lessa

Age and growth of the Spanish mackerel (Scomberomorus brasiliensis) caught off northeastern Brazil were determined. A total of 831 otoliths were examined - 296 from males (12 - 75 cm FL), 212 from females (11.5 - 72 cm FL) and 323 from specimens of undetermined sex (12.4 - 75 cm FL). There was a high percentage of juveniles in the catches, resulting mainly from the use of gillnets. Marginal increment analysis of the otoliths indicated that the shortest distances from the last ring to the edge occurred from November to May, laying down just one ring annually. One to eight rings were found, with specimen lengths ranging from 11.5 to 75.8 cm. The Schunute model was used to determine what model was best fit the data, demonstrating that the specialized von Bertalanffy growth equation is the most appropriate. Curves were established for males (L∞ = 79.52 cm, K = 0.189, t0 = -0.384 year) and females (L∞ = 109.18 cm, K = 0.114, t0 = -0.414 year), which resulted in distinct growth patterns between sexes. Based on the parameters estimated for the sexes separately, males have an approximate longevity of 15.5 years, whereas female longevity is 25.9 years. Specimens between 2 and 6 years of age represented 86% (n = 5,290) of the catch composition, characterizing the species as a catchable stock in the region. The present study updates essential information for assessing the stock of this important resource, for which the last growth studies in the region were carried out approximately thirty years ago.


2016 ◽  
Vol 5 (06) ◽  
pp. 4620
Author(s):  
Manal M. Khalifa ◽  
Ramadan A. S. Ali ◽  
Abdalla N. Elawad* ◽  
Mohammad El. ElMor

Age and growth characteristics of the thin-lipped Grey Mullet (Liza ramada) were investigated in Eastern coast of Libya. Aging was done by two methods: counting annuli on scales and by length frequency distribution, a total of 218 scales were studied for age determination, in addition of 334 fishes specimen for length frequency distribution reading. Four age groups were determined from scale reading, and five age groups from length frequency distribution methods, the parameters of the Von Bertalanffy growth equation for both sex of all individuals were estimated at 35.4 cm, 0.187 per year, -1.14 years and 2.4, for male were estimated at 35.7 cm, 0.17 per year, -1.367 and 2.3, for female were 38.6 cm, 0.156 per year, -1.383 and 2.4, for L∞, k and t0, and φ′, respectively.


Author(s):  
Silvina Botta ◽  
Eduardo R. Secchi ◽  
Mônica M.C. Muelbert ◽  
Daniel Danilewicz ◽  
Maria Fernanda Negri ◽  
...  

Age and length data of 291 franciscana dolphins (Pontoporia blainvillei) incidentally captured on the coast of Rio Grande do Sul State (RS), southern Brazil, were used to fit growth curves using Gompertz and Von Bertalanffy growth models. A small sample of franciscanas (N = 35) from Buenos Aires Province (BA), Argentina, were used to see if there are apparent growth differences between the populations. Male and female franciscana samples from both areas were primarily (78–85%) <4 years of age. The Von Bertalanffy growth model with a data set that excluded animals <1 year of age provided the best fit to data. Based on this model, dolphins from the RS population reached asymptotic length at 136.0 cm and 158.4 cm, for males and females, respectively. No remarkable differences were observed in the growth trajectories of males and females between the RS and BA populations.


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