Southern bluefin tuna populations in south-west Australia

1965 ◽  
Vol 16 (1) ◽  
pp. 25 ◽  
Author(s):  
JS Hynd

Length-frequency histograms of southern bluefin tuna caught for tagging and other purposes by F.V. Estelle Star in the course of survey operations showed heterogeneity in that the catches contained size groups, the differences between which could not be regarded as simply those to be expected between the age groups of a single stock. The times at which these groups appeared in the catches showed that the groups were characterized by distinct distributional behaviour, and this was confirmed by the results of the tagging operations. However, the groups are indistinguishable in their growth rate, so far as this has been shown by the present work, and no evidence is yet available as to the origins or status of these groups.

1970 ◽  
Vol 27 (7) ◽  
pp. 1265-1275 ◽  
Author(s):  
William Smoker ◽  
William G. Pearcy

Growth and reproductive patterns of the common lanternfish Stenobrachius leucopsarus (Eigenmann and Eigenmann) are described by length-frequency analysis, otolith analysis, and examination of ovaries. Length-frequency analysis showed that growth is approximately linear, 1.59 mm standard length per month, during the 2nd, 3rd, and part of the 4th year of life. Yearling fish average 23 mm long, 2-year-olds 41 mm, and 3-year-olds 59 mm.Otolith analyses indicate that some fish may live to be 8 years old, but confidence in this method is limited to fish 5 years old or younger. Fitting mean lengths of age-groups defined by otolith analyses with the von Bertalanffy equation gave L∞ = 85 mm, k = 0.34. Back calculation of lengths at the times of formation of otolith annuli gave another set of estimated mean lengths of age-groups, which, fitted by the von Bertalanffy equation, describes a growth curve similar to the one described by otolith analyses. The inflection in growth in weight occurs at about 4 years of age.Time of spawning, determined from egg measurements, occurs from December to March. Reproductively mature individuals are 4 years old and older. Recruitment of young size groups is also seasonal, 20- to 25-mm individuals appearing in largest proportions in trawl samples in the winter, presumably about 8 months after spawning.Comparison with other studies indicates that spawning may occur earlier in Monterey Bay, California, than off Oregon, but growth rates and sizes of age-groups I–V are similar. Comparisons with published results of otolith analyses show similar age determinations for the smaller size groups.


1990 ◽  
Vol 47 (2) ◽  
pp. 301-317 ◽  
Author(s):  
D. A. Fournier ◽  
John R. Sibert ◽  
Jacek Majkowski ◽  
John Hampton

We present a method for simultaneously analyzing multiple length frequency data sets. The method utilizes a robust likelihood-based estimation procedure that provides an objective criterion for hypothesis testing. The method is applied to length frequency data from southern bluefin tuna (Thunnus maccoyii) for which independent estimates of growth parameters based on tag return data are available. The estimates of the growth parameters from the new method were found to be in substantial agreement with the values previously obtained for these parameters. The strength of the likelihood approach is demonstrated by discriminating between alternative structural hypotheses for describing the data. The ability to simultaneously analyze multiple samples permits the method to exploit the extra information not available when analyzing samples one by one. The computer program maintains a database of fits to the data which enable the user to organize the results of the analysis. Graphical displays permit the user to view any of the fits, and an interactive graphics routine aids the user to find good initial parameter estimates.


2000 ◽  
Vol 51 (2) ◽  
pp. 143 ◽  
Author(s):  
George M. Leigh ◽  
William S. Hearn

Modal analysis is applied to historical length–frequency records of the Australian southern bluefin tunafishery, in order to quantify the variation in mean length from year to year. In the South Australian fishery in the first half of March, the mean length has ranged between 54 cm and 64 cm for 1-year-old fish, 73 cm and 85 cm for 2-year-old fish, and 85 cm and 100 cm for 3-year-old fish. The mean lengths of 2-, 3- and 4-year-old fish, and the increment from age 1 to age 3, have increased substantially over the history of the fishery. This increase in growth is probably a response to a decline in the population due to heavy fishing. In many years in the Western Australian fishery, two or more groups of 1-year-old fish were found: the mean lengths of these groups typically differed by 10 cm. Growth rates also varied markedly according to the season of the year.


2016 ◽  
Vol 5 (4) ◽  
pp. 345-352
Author(s):  
Damar Nusawicaksono Kurniawan ◽  
Abdul Ghofar ◽  
Suradi Wijaya Saputra ◽  
Bram Setyadji

ABSTRAK Pengkajian dan pendugaan status sumberdaya perikanan di suatu wilayah perairan dapat dilakukan dengan mengetahui laju eksploitasinya. Data frekuensi panjang merupakan salah satu data yang dapat digunakan untuk melakukan pendugaan tingkat eksploitasi tersebut. Penelitian ini bertujuan untuk menduga nilai mortalitas, laju pertumbuhan, ukuran pertama kali tertangkap dan tingkat eksploitasi. Penelitian dilakukan pada bulan April-Mei 2016 di Loka Penelitian Perikanan Tuna Pelabuhan Benoa, Denpasar, Bali. Metode yang digunakan adalah metode survei. Sementara data panjang ikan tuna sirip biru selatan tahun 2013-2014 kemudian diolah dengan perangkat lunak FISAT II. Hasil penelitian menunjukkan struktur ukuran ikan tuna sirip biru selatan 145 - 210 cmFL dengan modus di ukuran 170-174 cmFL, ukuran pertama kali tertangkap (Lc) 171 cmFL, hubungan panjang berat mendapat nilai W= 0,00006*FL2,792, faktor kondisi berada pada angka 1,86-2,00, laju pertumbuhan yang didapat yaitu Lt=220,50(1 - e 0,2(t+0,488)), dimana nilai dari L∞ yaitu 220,50 cmFL dan nilai t0 -0,49, laju mortalitas total (Z) sebesar 1,14/tahun, laju mortalitas alami (M) sebesar 0,36/tahun, dan laju mortalitas akibat penangkapan (F) sebesar 0,78/tahun, dan tingkat eksploitasi (E) 0,68/tahun, Hal ini menunjukan penangkapan  ikan tuna sirip biru selatan oleh kapal rawai tuna di Samudera Hindia dalam keadaan berlebih (overfishing) karena nilai tingkat eksploitasi yang didapat melebihi tingkat pemanfaatan optimum atau Eopt = 0,5/tahun (0,68 > 0,5). Kata Kunci : Ikan Tuna Sirip Biru Selatan, Tingkat Eksploitasi, Mortalitas, Pertumbuhan  ABSTRACT Stock assessment and prediction status of fisheries resources in the waters can be made by knowing the rate of exploitation. Length-frequency data is one can be used to suspect rate of exploitation . The aimed of this research was to suspect value of mortality, the growth rate, size at first capture and the level of exploitation. This research was conducted on April-May 2016 at the Loka Fishery Tuna's Research Benoa Port, Denpasar, Bali. This research used survey method.While data length of the southern bluefin tuna 2013-2014 was processed with FISAT II. The results showed size structure of southern bluefin tuna 145-210 cmFL with mode in sizes 170-174 cmFL, size at first capture (Lc) 171 cmFL, value of lenght and weight relationship W = 0,00006 *,792 FL2, condition factors 1,86-2.00, the growth rate Lt = 220,50 (1-e of 0.2 (t + 0,488)), where the value of L ∞ was 220.50 cmFL and value t0 -0.49 total mortality rate (Z) of 1.14/year, rate of natural mortality (M) of 0.36/year, and  rate of mortality due to the arrest of (F) amounted to 0.78/year, and the rate of exploitation (E) 0,68/year, it shows the fishing of southern bluefin tuna by the longline in the Indian Ocean was overfishing because level of exploitation value was over the optimum effort or Eopt = 0,5/year (0.68 > 0.5). Keyword: Southern Bluefin Tuna, exploitation rate, Mortality, growth,


2004 ◽  
Vol 61 (2) ◽  
pp. 292-306 ◽  
Author(s):  
J Paige Eveson ◽  
Geoff M Laslett ◽  
Tom Polacheck

A maximum likelihood method for modelling fish growth is presented that integrates data from three key sources of growth information: tag–recapture studies, length–frequency samples from commercial catches, and direct aging data from hard-parts analyses. Previous studies have almost exclusively modelled growth using only one of these sources of information. Different data sources are often most informative about different portions of the life cycle. The development of an integrated approach allows for the different data sources to complement each other and provide more comprehensive and robust estimates of growth parameters. The integrated method is applied to data sets from southern bluefin tuna (Thunnus maccoyii) using the von Bertalanffy growth curve as well as a more sophisticated growth curve that makes a smooth transition between two von Bertalanffy curves with different growth rate parameters. The latter is found to provide a significantly better fit and supports previous findings that southern bluefin tuna experience a transition in growth during the juvenile stage of life. Many species exhibit a seasonal growth pattern, including southern bluefin tuna for which growth is fastest during the austral summer. A method for incorporating an annual seasonal component into the analysis is described and applied.


1991 ◽  
Vol 48 (8) ◽  
pp. 1358-1363 ◽  
Author(s):  
Greg P. Jenkins ◽  
Jock W. Young ◽  
Tim L. O. Davis

Competition for food among larvae and subsequent reduction in growth rates has been proposed as a mechanism to explain the apparent density-dependent control of some exploited marine fish populations, but has received little support from field data. Growth of larvae of southern bluefin tuna, Thunnus maccoyii, in the East Indian Ocean was significantly different among stations sampled randomly within a 20-km radius. Growth rate was positively correlated with feeding rate but not with temperature, indicating that larvae were food limited to a varying degree. A negative correlation between growth rate and abundance suggested that food limitation was density dependent. Regression analysis indicated that in areas of highest larval densities there was an approximate 25% reduction in growth rate. We suggest that in areas of high abundance, larvae were competing for food, leading to a density-dependent reduction of growth rate. Because the larval stage of high mortality is prolonged, cumulative mortality of slow-growing larvae over this period may be greater, even if the mortality rate is constant.


Fisheries ◽  
2020 ◽  
Vol 2020 (6) ◽  
pp. 108-110
Author(s):  
Viacheslav Zharnikov ◽  
Andrey Smirnov

The growth of various size groups of mussels in the Veselaya Bay of the tauyskaya Bay, grown in mono - and polyculture in suspended cages in the sea, was analyzed. The maximum growth was observed in mussels of the size group 10-20 mm at the age of 2 years. Shellfish grew more slowly at the age of 3-5 years. The growth rate of mollusks of all size groups in the polyculture was higher than in the monoculture. The percentage of elimination of mussels of all age groups in the polyculture was significantly lower. The forecast of growth of mussels of various size groups in poly - and monoculture in suspended cages in the first, second and third growth seasons in Veselaya Bay is made. The efficiency of cultivation of mussels in the Northern part of the sea of Okhotsk together with other edible mollusks: makoma and Miya is shown.


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