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

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.

1992 ◽  
Vol 43 (5) ◽  
pp. 983 ◽  
Author(s):  
JR Anderson ◽  
AK Morison ◽  
DJ Ray

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.


1992 ◽  
Vol 43 (5) ◽  
pp. 1103 ◽  
Author(s):  
JR Anderson ◽  
AK Morison ◽  
DJ Ray

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.


Author(s):  
Jonah L Withers ◽  
Dimitry Gorsky ◽  
Zy Biesinger ◽  
Donald Einhouse ◽  
Michael Clancy ◽  
...  

Knowledge of the distribution of ages of fish within a stock, and subsequently individual growth rates, allows managers the ability to calculate key metrics (i.e., recruitment, mortality, and stock growth rate) that greatly improve stock assessment models. Two remnant stocks of Lake Sturgeon Acipenser fulvescens exist near and within the Niagara River; one primarily occupying the headwaters of the river and the other primarily occupying the mouth of the river. Though initial efforts in the late 1990s collected data on the lower Niagara River stock, a long-term, comprehensive examination of age and growth is lacking and the age structure of the stock found at the headwaters has yet to be formally described to our knowledge. To ascertain the current age structure of these two stocks we sampled Lake Sturgeon in the lower Niagara River and at the headwaters of the Niagara River between 2012 and 2017 and took a portion of the leading pectoral fin spine of captured Lake Sturgeon for age estimation. Ages ranged between 4 and 42 years with females generally being older and larger than males. The median age appeared to increase from 14 to 18 years old throughout our study in both stocks. Lengths-at-age of both stocks were larger than those reported in other systems and growth rates appear to have increased over the past decade in the lower Niagara River. Despite efforts to improve age estimation accuracy, age estimates from fish whose ages were partly-known (derived from multiple age estimates from fish that were captured multiple times) demonstrated assigned ages may have greater error than expected. Additionally, a lack of young individuals confounded growth analyses. Although there was uncertainty in the assigned ages, this study still provides evidence of consistent recruitment in both stocks and, to our knowledge, the first characterization of the age structure of the Lake Sturgeon stock occupying the headwaters of the Niagara River.


2012 ◽  
Vol 69 (11) ◽  
pp. 1850-1869 ◽  
Author(s):  
Allen H. Andrews ◽  
Edward E. DeMartini ◽  
Jon Brodziak ◽  
Ryan S. Nichols ◽  
Robert L. Humphreys

Growth characteristics of Pristipomoides filamentosus, a deepwater eteline snapper of major economic importance, are incomplete and inconsistent across its geographical range. Early growth rates have been validated using daily increment and length–frequency analyses, but historical estimates of adult growth rates are variable and longevity is unknown. Studies of P. filamentosus in the Hawaiian Islands have cautioned against unjustified estimates of longevity, but 18 years has at times been uncritically assumed as the maximum age. The present study addresses these age, growth, and longevity issues using lead–radium and bomb radiocarbon dating by providing valid age estimates for adult P. filamentosus. Valid length-at-age estimates ranged from approximately 10 years to more than 40 years. These data, together with robust daily increment data, were used to model a fully validated, long-lived life history for P. filamentosus. This study adds to the few existing studies supporting a view that many tropical fishes, particularly deepwater species, can be longer lived than previously surmised.


2016 ◽  
Vol 73 (10) ◽  
pp. 1575-1586 ◽  
Author(s):  
Allen H. Andrews ◽  
Edward E. DeMartini ◽  
Jeff A. Eble ◽  
Brett M. Taylor ◽  
Dong Chun Lou ◽  
...  

Bluespine unicornfish (Naso unicornis) from Hawaii were aged to >50 years using cross-sectioned sagittal otoliths. Fish length was a poor indicator of age because of rapid and variable early growth, exemplified by fish aged to be 4 years near maximum length. Growth was deterministic with adult ages decoupled from body length. Otolith mass and thickness were evaluated as proxies for age and both were encouraging; thickness explained more variance but mass was easier to measure. An age estimation protocol was validated through ontogeny using bomb radiocarbon (14C) dating. Use of the postbomb 14C decline period from a regional reference chronology enabled age validation of young fish — a novel approach for the Pacific Ocean. A probabilistic procedure for assigning bomb 14C dates (CALIBomb) was used for the first time to determine fish birth years. The age-reading protocol was generally validated, and it was possible to describe length-at-age despite difficulties in counting otolith annuli beyond 30–40 years. Growth curves differed between the sexes, and a four-parameter generalized von Bertalanffy growth function provided the best fit.


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.


2018 ◽  
Vol 59 (1) ◽  
pp. 97-110 ◽  
Author(s):  
Mado Kotsiri ◽  
Ioannis E. Batjakas

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.


2018 ◽  
Vol 31 (2) ◽  
pp. 429-441
Author(s):  
Arsalan ◽  
Muhammad Faheem Siddiqui ◽  
Moinuddin Ahmed ◽  
Syed Shahid Shaukat ◽  
Alamdar Hussain

2012 ◽  
Vol 9 (3) ◽  
pp. 1253-1265 ◽  
Author(s):  
P. Sabatier ◽  
J.-L. Reyss ◽  
J. M. Hall-Spencer ◽  
C. Colin ◽  
N. Frank ◽  
...  

Abstract. Here we show the use of the 210Pb-226Ra excess method to determine the growth rate of two corals from the world's largest known cold-water coral reef, Røst Reef, north of the Arctic circle off Norway. Colonies of each of the two species that build the reef, Lophelia pertusa and Madrepora oculata, were collected alive at 350 m depth using a submersible. Pb and Ra isotopes were measured along the major growth axis of both specimens using low level alpha and gamma spectrometry and trace element compositions were studied. 210Pb and 226Ra differ in the way they are incorporated into coral skeletons. Hence, to assess growth rates, we considered the exponential decrease of initially incorporated 210Pb, as well as the increase in 210Pb from the decay of 226Ra and contamination with 210Pb associated with Mn-Fe coatings that we were unable to remove completely from the oldest parts of the skeletons. 226Ra activity was similar in both coral species, so, assuming constant uptake of 210Pb through time, we used the 210Pb-226Ra chronology to calculate growth rates. The 45.5 cm long branch of M. oculata was 31 yr with an average linear growth rate of 14.4 ± 1.1 mm yr−1 (2.6 polyps per year). Despite cleaning, a correction for Mn-Fe oxide contamination was required for the oldest part of the colony; this correction corroborated our radiocarbon date of 40 yr and a mean growth rate of 2 polyps yr−1. This rate is similar to the one obtained in aquarium experiments under optimal growth conditions. For the 80 cm-long L. pertusa colony, metal-oxide contamination remained in both the middle and basal part of the coral skeleton despite cleaning, inhibiting similar age and growth rate estimates. The youngest part of the colony was free of metal oxides and this 15 cm section had an estimated a growth rate of 8 mm yr−1, with high uncertainty (~1 polyp every two to three years). We are less certain of this 210Pb growth rate estimate which is within the lowermost ranges of previous growth rate estimates. We show that 210Pb-226Ra dating can be successfully applied to determine the age and growth rate of framework-forming cold-water corals if Mn-Fe oxide deposits can be removed. Where metal oxides can be removed, large M. oculata and L. pertusa skeletons provide archives for studies of intermediate water masses with an up to annual time resolution and spanning over many decades.


1964 ◽  
Vol 44 (3) ◽  
pp. 315-319
Author(s):  
J. M. Bell

Growth records were obtained from 12 research establishments across Canada for pigs fed according to current (1960–63) recommendations of nutrition and management. Growth curves showing age in days and weight in pounds are presented for the various breeds and crossbreds, for between-station comparisons, for comparison of upper and lower quartiles in purebred pigs, and for comparison of growth rates of purebreds with that of Yorkshires of 20 to 25 years ago.Age at 200 lb averaged from 152 to 187 days, among 10 stations for the Yorkshire breed. Pigs of each of the pure breeds reached 200 lb about 3 weeks earlier than that indicated in previous studies. Crossbred pigs of each of four different crosses grew more rapidly than average Yorkshires, some reaching 200 lb in 140 days and having gains in excess of 2.3 lb/day during the finishing period. Yorkshire, Lacombe, and Landrace pigs had similar growth curves. The upper quartile averaged 1.8 and the lower 1.4 lb/day gain between 100 and 200 lb weights. Slow-maturing pigs tended to be below average throughout life but differences in maturity between stations seemed to reflect differing rates of gain in early life, since finishing period gains were similar in 8 of 10 stations.


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