scholarly journals Life history of Patagonian squid Loligo gahi and growth parameter estimates using least-squares fits to linear and von Bertalanffy models

1988 ◽  
Vol 47 ◽  
pp. 65-74 ◽  
Author(s):  
KR Patterson
Author(s):  
Ivelina Yordanova Zlateva ◽  
Nikola Nikolov

Advanced in the present article is a Two-step procedure designed on the methods of the least squares (LS) and instrumental variable (IV) techniques for simultaneous estimation of the three unknown parameters L∞, K and t0, which represent the individual growth of fish in the von Bertalanffy growth equation. For the purposes of the present analysis, specific MATLAB-based software has been developed through simulated data sets to test the operational workability of the proposed procedure and pinpoint areas of improvement. The resulting parameter estimates have been analyzed on the basis of consecutive comparison (the initial conditions being the same) between the results delivered by the two-step procedure for simultaneous estimation of L∞, K and t0 and the results obtained via the most commonly employed methods for estimating growth parameters; first, use has been made of the Gulland-and-Holt method for estimating the asymptotic length L∞and the curvature parameter K, followed by the von Bertalanffy method for estimation of t0.


2022 ◽  
Vol 8 ◽  
Author(s):  
Shui-Kai Chang ◽  
Tzu-Lun Yuan ◽  
Simon D. Hoyle ◽  
Jessica H. Farley ◽  
Jen-Chieh Shiao

Growth shapes the life history of fishes. Establishing appropriate aging procedures and selecting representative growth models are important steps in developing stock assessments. Flyingfishes (Exocoetidae) have ecological, economic, and cultural importance to many coastal countries including Taiwan. There are 29 species of flyingfishes found in the Kuroshio Current off Taiwan and adjacent waters, comprising 56% of the flyingfishes taxa recorded worldwide. Among the six dominant species in Taiwan, four are of special importance. This study reviews aging data of these four species, documents major points of the aging methods to address three aging issues identified in the literature, and applies multi-model inference to estimate sex-combined and sex-specific growth parameters for each species. The candidate growth models examined included von Bertalanffy, Gompertz, Logistic, and Richards models, and the resulting optimal model tended to be the von Bertalanffy model for sex-combined data and Gompertz and von Bertalanffy models for sex-specific cases. The study also estimates hatch dates from size data collected from 2008 to 2017; the results suggest that the four flyingfishes have two spawning seasons per year. Length-weight relationships are also estimated for each species. Finally, the study combines the optimal growth estimates from this study with estimates for all flyingfishes published globally, and statistically classifies the estimates into clusters by hierarchical clustering analysis of logged growth parameters. The results demonstrate that aging materials substantially affect growth parameter estimates. This is the first study to estimate growth parameters of flyingfishes with multiple model consideration. This study provides advice for aging flyingfishes based on the three aging issues and the classification analysis, including a recommendation of using the asterisci for aging flyingfishes to avoid complex otolith processing procedures, which could help researchers from coastal countries to obtain accurate growth parameters for many flyingfishes.


1997 ◽  
Vol 54 (9) ◽  
pp. 2025-2032
Author(s):  
E B Smith ◽  
F M Williams ◽  
C R Fisher

The effects of intrapopulation variability on the parameter estimates of the von Bertalanffy growth equation have received discussion in the literature. Here we evaluated the effects of intrapopulation variability, using computer simulations, on four commonly used methods for estimating the von Bertalanffy growth parameters: the Ford-Walford plot, Ricker's method, Bayley's method, and Fabens' method. Intrapopulation variability in growth rates (k) and maximum sizes ( L infinity ) plus initial size distributions and measurement error, were tested for their effects on the accuracy of the parameter estimates using simulated mark-recapture data with equal recapture intervals. Fabens' method and a modified Ford-Walford plot provided the most accurate estimates in all cases, but when intrapopulation variability was large, they performed poorly. With moderate intrapopulation variability, the bias in estimates was small although between-sample variance was quite large. Biased initial size distributions without either small or large size classes cause a magnification of the estimation errors. Without knowledge of the degree of intrapopulation variability in a natural population, large errors of unknown magnitude in parameter estimation can result, and care should be taken when interpreting these estimates. However, if this variability can be quantified, then approximate parameter estimate errors can be obtained.


2021 ◽  
Vol 657 ◽  
pp. 191-207
Author(s):  
MD Ramirez ◽  
T Popovska ◽  
EA Babcock

Knowledge of sea turtle demographic rates is central to modeling their population dynamics, but few studies have quantitatively synthesized existing data globally. Here, we used a Bayesian hierarchical model to conduct a meta-analysis of published von Bertalanffy growth curve parameters (growth coefficient, K; asymptotic length, L∞) for chelonid sea turtles. We identified 34 studies for 5 of 6 extant chelonids that met minimum selection criteria. We implemented a suite of models that included a multivariate normal likelihood on the log-transformed values of the 2 parameters to evaluate the influence of species, population (regional management unit, RMU), parameter estimation method (mark-recapture, skeletochronology, length-frequency analysis), latitude, and sampled body size range (all sizes, no large, no small, no large or small) on growth parameter estimates. According to information criteria, the best model included a random effect of species. The second best model also included latitude as a fixed effect, but RMU, parameter estimation method, latitude, and sampled body size ultimately did not strongly influence the means or variances of K and L∞ among studies. The apparent lack of RMU effect on parameter estimates within species may be an artifact of the small number of RMUs with published growth parameter estimates. The species-specific, and in some cases RMU-specific, posterior means and standard deviations of K and L∞ from this study would be appropriate priors for future studies of growth in chelonid sea turtles or for models of population dynamics. We highlight the need for expanded study and synthesis of sea turtle somatic growth rates.


2006 ◽  
Vol 57 (3) ◽  
pp. 313 ◽  
Author(s):  
Kristy L. Forsgren ◽  
Christopher G. Lowe

The aim of this study was to provide a detailed description of the life history of weedy seadragons, Phyllopteryx taeniolatus. Weedy seadragon development was described based on morphological characters and categorised into four periods: incubation, larval, juvenile and sub-adult. Hatching occurred 35–42 days post-fertilisation, most hatchlings exhibited juvenile characteristics upon hatching or shortly thereafter. The von Bertalanffy growth parameters generated from weedy seadragon length-at-age data were L ∞ = 285 ± 3 mm standard length (SL; mean ± s.e.) and k = 2.20 ± 0.05 year−1. Females possessed a higher gonosomatic index (GSI; 1.25 ± 1.18%; mean ± s.d.) than males (0.34 ± 0.20%), which increased substantially for females over 230 mm in length. Mature female weedy seadragons (290 ± 32 mm SL) ovulated 110 ± 27 eggs per female per spawning. Additionally, three females produced more than one clutch per season. Male weedy seadragons (319 ± 9 mm SL) successfully incubated 91 ± 40 eggs per spawning event. In addition to improving our understanding of the life history of weedy seadragons, this information can be used to estimate population demography and develop management strategies.


1992 ◽  
Vol 43 (5) ◽  
pp. 1229 ◽  
Author(s):  
K.R. Rowling ◽  
DD Reid

Estimates of von Bertalanffy growth parameters were made for mature (>3-year-old) gemfish (Rexea solandri), using otoliths sampled biennially from commercial catches between 1980 and 1986. During this period, there was a significant decline in the mean length of mature gemfish in the catch. Large variations in growth-parameter estimates were found over the period sampled (e.g. L∞ ranged between 87.3 and 130.3 cm for males and between 113.1 and 134.7 cm for females). Likelihood-ratio tests showed many of the growth-parameter estimates to be significantly different between the years sampled. Inclusion in the analyses of data for juvenile (1- to 3-year-old) fish considerably reduced both the standard errors of the parameter estimates and the significance of the variations between them. Comparison of parameters estimated by following the growth of individual cohorts spawned in 1975 and 1981 suggested that the variations in the parameters for the 1980-86 data were caused by differences in the length composition of the samples rather than by changes in the growth rate of the fish. The results suggest the need for care when comparing growth parameters estimated for different populations, especially when there are large differences in length composition. The best estimates of growth parameters for gemfish were considered to be those derived from the aggregate data for the whole of the period sampled, including the data for juveniles. For male gemfish these best estimates (with asymptotic standard errors in parentheses) were L∞ =97.5 (0.8) cm, K=0.212 (0.005) year-1 and to = - 0.54 (0.05) years, and for females the estimates were L∞ = 109.4 (0.6) cm, K= 0.180 (0.003) year-1 and to= -0.63 (0.04) years. Likelihood-ratio tests showed these estimates of L∞ and K to be significantly different between the sexes.


2018 ◽  
Vol 69 (4) ◽  
pp. 562 ◽  
Author(s):  
Michael I. Grant ◽  
Jonathan J. Smart ◽  
William T. White ◽  
Andrew Chin ◽  
Leontine Baje ◽  
...  

In the central west Pacific region, silky sharks (Carcharhinus falciformis) are commonly taken in fisheries, forming up to 95% of incidental elasmobranch bycatch. The present study examined the life history of silky sharks (n=553) from Papua New Guinean waters. Age was analysed using sectioned vertebrae, and a multimodel approach was applied to the length-at-age data to fit growth models. Females ranged in length from 65.0- to 253.0-cm total length (TL), with the oldest estimated at 28 years. Males ranged in length from 68.4 to 271.3cm TL and were aged to a maximum of 23 years. The logistic model provided the best fitting growth parameter estimates of length at birth L0=82.7cm TL, growth coefficient g=0.14year–1 and asymptotic length L∞=261.3cm TL for the sexes combined. Females reached sexual maturity at 204cm TL and 14.0 years, whereas males reached maturity at 183cm TL and 11.6 years. The average litter size from 28 pregnant females was 8 (range of 3–13). The growth parameters and late ages of sexual maturation for silky sharks in the central west Pacific suggest a significant risk from fisheries exploitation without careful population management.


2013 ◽  
Vol 64 (10) ◽  
pp. 965 ◽  
Author(s):  
Andrew Chin ◽  
Colin Simpfendorfer ◽  
Andrew Tobin ◽  
Michelle Heupel

Inadequate life-history information can compromise management of shark populations. The present study examined the life history of blacktip reef sharks (Carcharhinus melanopterus) from north-eastern Australia with predictions that they would show life-history patterns similar to those of other reef sharks species. Age and growth estimates were derived from vertebrae and five growth models. Males were 543–1390 mm total length (LST) and females were 514–1600 mm LST. Longevity was 10 years (males) and 15 years (females). Chemical marking confirmed annual band pair deposition but indicated probable age underestimation of large individuals. The logistic model was preferred (second-order Akaike information criterion (AICc) weight 0.7536), with growth parameter estimates of length at birth (L0) = 617 mm LST; asymptotic length (L∞) = 1585 mm LST; k (from logistic model) = 0.251 year–1. Males matured at 4.2 years (1050 mm LST) and females at 8.5 years (1335 mm LST), although further verification is needed. Mating and parturition occurred in summer and autumn, females having three or four pups per litter. Data were inconclusive in determining reproductive periodicity. These data contribute to the species management and conservation and suggest that the species may be sensitive to fishing pressure and habitat loss. The study also demonstrated potential complications in using vertebrae to estimate age and growth of chondrichthyan fishes.


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