scholarly journals Age and growth of franciscana dolphins, Pontoporia blainvillei (Cetacea: Pontoporiidae) incidentally caught off southern Brazil and northern Argentina

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.

2007 ◽  
Vol 5 (4) ◽  
pp. 485-490 ◽  
Author(s):  
Giovana Bervian ◽  
Nelson F. Fontoura

The growth of Atherinella brasiliensis (Quoy & Gaimard, 1824) was studied through monthly samples taken at Tramandaí Lagoon, Imbé County, Rio Grande do Sul, Brazil. Animals were captured using a beach seine net. Length-weight relationships and age- growth curves for males and females were adjusted. The growth parameters of the von Bertalanffy growth formulae are Linf=16.0 and k=0.883 for males and Linf=17.0 and k=0.825 for females. First reproduction occurred one year after recruitment. Once reaching maturity, adults of A. brasiliensis reproduced once more in the next spring with two-year-olds and disappeared soon after from size frequency distributions. A few captured animals showed a size compatible with an age of three years.


2013 ◽  
Vol 91 (9) ◽  
pp. 672-677 ◽  
Author(s):  
D.C. Knickle ◽  
G.A. Rose

Growth and maturity of two sympatric gadids were examined from 48 Atlantic (Gadus morhua L., 1758) and 42 Greenland (Gadus ogac Richardson, 1836) cod ranging from 17 to 74 cm in length collected from an inshore area of Trinity Bay, Newfoundland, Canada, during 2009 and 2010. Ages estimated from otolith readings ranged from 2 to 7 for both species. Age and size at 50% maturity differed between species, being 2.3 years and 28.2 cm for G. ogac and 4.6 years and 48.8 cm for G. morhua. von Bertalanffy growth models did not differ between species with parameters L∞ = 91 cm, k = 0.16 year−1, t0 = –0.02 years for G. ogac and L∞ = 112 cm, k = 0.13 year−1, t0 = 0.18 years for G. morhua. Length (L) – mass (W) relationships differed; W = 0.000005 kg·cm−b × L3.17 for G. ogac and W = 0.000011 kg·cm−b × L2.91 for G. morhua suggested slightly positive and negative allometric growth, respectively. For G. morhua, growth curves, length–mass relationships, and maturity rates did not differ between fish collected during this and earlier studies. Differences in maturity schedules and growth may decrease resource competition and help facilitate coexistence of these species.


2013 ◽  
Vol 48 (8) ◽  
pp. 975-982 ◽  
Author(s):  
Gustavo Ruschel Lopes ◽  
Carlos Henrique Araujo de Miranda Gomes ◽  
Cláudio Rudolfo Tureck ◽  
Claudio Manuel Rodrigues de Melo

The objective of this work was to evaluate the growth of the mangrove oyster Crassostrea gasar cultured in marine and estuarine environments. Oysters were cultured for 11 months in a longline system in two study sites - São Francisco do Sul and Florianópolis -, in the state of Santa Catarina, Southern Brazil. Water chlorophyll-α concentration, temperature, and salinity were measured weekly. The oysters were measured monthly (shell size and weight gain) to assess growth. At the end of the culture period, the average wet flesh weight, dry flesh weight, and shell weight were determined, as well as the distribution of oysters per size class. Six nonlinear models (logistic, exponential, Gompertz, Brody, Richards, and Von Bertalanffy) were adjusted to the oyster growth data set. Final mean shell sizes were higher in São Francisco do Sul than in Florianópolis. In addition, oysters cultured in São Francisco do Sul were more uniformly distributed in the four size classes than those cultured in Florianópolis. The highest average values of wet flesh weight and shell weight were observed in São Francisco do Sul, whereas dry flesh weight did not differ between the sites. The estuary environment is more promising for the cultivation of oysters.


2021 ◽  
Vol 19 (2) ◽  
Author(s):  
Leandro Balboni ◽  
Facundo Vargas ◽  
Darío Colautti

Abstract The age and growth of Pseudoplatystoma corruscans, is analyzed on specimens landed in Puerto Antequera, Province of Chaco, Argentina. The study is based on length frequency distribution of 1192 individuals and growth marks of 293 pectoral spines. Previously to age assignation based on spines readings, we performed analyses that ruled out age-associated resorption of rings and corroborated the annual periodicity of mark formation. The average sizes of the radius of each ring were obtained, and the total length of fish were back-calculated to the time of the ring formation, by the regression model fitted between the total radius of the spines to the respective sizes of each fish. Such data showed a good fitting to growth models of von Bertalanffy, Gompertz and logistic for both sexes separately. Results indicate that the study of the species growth must be carried out for each sex separately and that the fishing regulations must consider this characteristic of the species since the current management guidelines could be promoting differential capture by sexes.


2011 ◽  
Vol 9 (2) ◽  
pp. 393-401 ◽  
Author(s):  
Marília Previero ◽  
Carolina V. Minte-Vera ◽  
Matheus Oliveira Freitas ◽  
Rodrigo Leão de Moura ◽  
Claudenice Dei Tos

We determined the age and growth of the dog snapper (Lutjanus jocu), caught in the region of Abrolhos Bank, Bahia State, by the fishermen from coastal communities of Prado, Alcobaça, Caravelas, and Nova Viçosa. We examined 205 sectioned otoliths of fish caught by harpoon, longline, hand line, and gill nets (14.5 to 79.5 cm fork length). The formation of each ring was considered annual. The sectioned otoliths showed between 0 and 29 rings. Nearly half of the analyzed specimens had between 0 and 7 rings (88 of 205). Fish caught with nets in the estuarine region were the juvenile, while fish caught with lines and harpoons were the oldest. Two von Bertalanffy growth models were fitted to length-at-age data: one assuming constant variance of length-at-age (SVB) and another assuming constant coefficient of variation, i.e. variance increasing as a function of average size (CVVB). The SVB estimates were Loo = 87.82 cm, K = 0.10, and t0 = -1.486 and the CVVB estimates were Loo = 117.60 cm, K = 0.06, and t0 = -2.470. The largest Loo values estimated by the CVVB model are supported by reports from the literature of larger animals occurring in the deeper outer shelf of Abrolhos Bank. Growth parameters were also estimated for males and females separately (SVB model) (Loo = 92.80 cm, K = 0.099, and t0 = -1.680 for males, and Loo = 82.10 cm, K = 0.105, and t0 = -1.570 for females).


PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e2431 ◽  
Author(s):  
Joshua Hatch ◽  
Yan Jiao

Inferring growth for aquatic species is dependent upon accurate descriptions of age-length relationships, which may be degraded by measurement error in observed ages. Ageing error arises from biased and/or imprecise age determinations as a consequence of misinterpretation by readers or inability of ageing structures to accurately reflect true age. A Bayesian errors-in-variables (EIV) approach (i.e., measurement-error modeling) can account for ageing uncertainty during nonlinear growth curve estimation by allowing observed ages to be parametrically modeled as random deviates. Information on the latent age composition then comes from the specified prior distribution, which represents the true age structure of the sampled fish population. In this study, weakfish growth was modeled by means of traditional and measurement-error von Bertalanffy growth curves using otolith- or scale-estimated ages. Age determinations were assumed to be log-normally distributed, thereby incorporating multiplicative error with respect to ageing uncertainty. The prior distribution for true age was assumed to be uniformly distributed between ±4 of the observed age (yr) for each individual. Measurement-error growth models described weakfish that reached larger sizes but at slower rates, with median length-at-age being overestimated by traditional growth curves for the observed age range. In addition, measurement-error models produced slightly narrower credible intervals for parameters of the von Bertalanffy growth function, which may be an artifact of the specified prior distributions. Subjectivity is always apparent in the ageing of fishes and it is recommended that measurement-error growth models be used in conjunction with otolith-estimated ages to accurately capture the age-length relationship that is subsequently used in fisheries stock assessment and management.


PLoS ONE ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. e0246734
Author(s):  
Jonathan J. Smart ◽  
Gretchen L. Grammer

Growth modelling is a fundamental component of fisheries assessments but is often hindered by poor quality data from biased sampling. Several methods have attempted to account for sample bias in growth analyses. However, in many cases this bias is not overcome, especially when large individuals are under-sampled. In growth models, two key parameters have a direct biological interpretation: L0, which should correspond to length-at-birth and L∞, which should approximate the average length of full-grown individuals. Here, we present an approach of fitting Bayesian growth models using Markov Chain Monte Carlo (MCMC), with informative priors on these parameters to improve the biological plausibility of growth estimates. A generalised framework is provided in an R package ‘BayesGrowth’, which removes the hurdle of programming an MCMC model for new users. Four case studies representing different sampling scenarios as well as three simulations with different selectivity functions were used to compare this Bayesian framework to standard frequentist growth models. The Bayesian models either outperformed or matched the results of frequentist growth models in all examples, demonstrating the broad benefits offered by this approach. This study highlights the impact that Bayesian models could provide in age and growth studies if applied more routinely rather than being limited to only complex or sophisticated applications.


2018 ◽  
Vol 20 (1) ◽  
pp. 85-90 ◽  
Author(s):  
GOPALAN MAHADEVAN ◽  
PALANIVEL BHARATHIRAJAN ◽  
VELAYUTHAM RAVI ◽  
MOJTABA POULADI ◽  
MARYAM MIRZAEI VAND KHANGHAH

Mahadevan G, Bharathirajan P, Ravi V, Pouladi M, Mirzaei Vand Khanghah M. 2019. Short Communication: Age and growth of elongated mudskipper, Pseudapocryptes elongatus (Cuvier, 1816) from Sundarbans, India. Biodiversitas 20: 85-90. The estimation of age and mathematical expression of fish growth is complex and debated subject in fishery sciences. Growth parameters of elongated mudskipper, Pseudapocryptes elongatus were estimated based on the length frequency data using FiSAT II software (several tools such as Powell-Wetherall method, ELEFAN and von Bertalanffy growth estimates). Samples were collected from Sundarbans mangroves using gill and cast nets and by hand picking. The length-frequency (LFQ) of P.elongatus was recorded from January 2014 to December 2015 and the above tools estimated the growth parameters (L∞, K and t0) from the progression of LFQ modes through time. L∞ and K values of males were 220.50 mm and 1.3 yr-1, respectively and similarly, L∞ and K values of females were 221.05 mm and 1.21 yr-1, respectively. The t0 values estimated for males and females were-0.1915 years and-0.1661 years, respectively. The estimated growth performance index (Φ) values for males and females of P. elongatus were 4.394 and 4.503, respectively. The lifespan of both the sexes was found to be 4+ years.


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.


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


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