Otoliths of Chinook Salmon (Oncorhynchus tshawytscha): Daily Growth Increments and Factors Influencing Their Production

1982 ◽  
Vol 39 (10) ◽  
pp. 1340-1347 ◽  
Author(s):  
John D. Neilson ◽  
Glen H. Geen

The effects of photoperiod, feeding frequency, and water temperature on formation of otolith daily growth increments in juvenile chinook salmon (Oncorhynchus tshawytscha) were examined. Feeding frequency influenced both increment number and width, whereas photoperiod and temperature affected only increment width. Fish fed once/24 h produced one increment every 24 h on average, while fish fed 4 times/24 h produced more than one increment every 24 h. Wider increments were produced in fish exposed to warmer water (11 °C) or 24 h of darkness. The ratio of otolith size to fish size remained constant throughout and between the photoperiod, temperature, and feeding frequency experiments, regardless of the number or width of increments produced. Although otolith growth is isometric with respect to increase in fish length under these experimental regimes, otolith microstructure will differ in fish of the same size reared under different environmental conditions. An understanding of factors affecting otolith increment production is required before increment number and width can be used to assess growth rates.Key words: otolith, daily, growth increments, chinook salmon

1985 ◽  
Vol 63 (1) ◽  
pp. 22-27 ◽  
Author(s):  
G. H. Geen ◽  
J. D. Neilson ◽  
M. Bradford

Chinook salmon (Oncorhynchus tshawytscha) eggs, alevins, and fry were reared in pH 4.5, 5.0. 5.5, 6.2 (control), and 7.0 water from the eyed stage of development. Survival through hatching was >90% in all instances. Alevin mortality was high at pH 4.5 and 5.0. Fry were more tolerant of low pH than alevins. Growth rates of alevins and fry held at or above pH 5.0 and 4.5, respectively, were not affected by pH, nor did exposure to acidic water retard otolith development or result in their resorption. One otolith daily growth increment was formed every 24 h in alevins and fry irrespective of pH. Widths of otolith daily growth increments decreased when fry were transferred to pH 4.5 water and increased on their return to higher pH indicating changes in growth rate. Transfer of fry from pH 6.2 to pH 5.0 or 5.5 had no effect on increment widths.


2007 ◽  
Vol 64 (12) ◽  
pp. 1683-1692 ◽  
Author(s):  
Rachel Barnett-Johnson ◽  
Churchill B Grimes ◽  
Chantell F Royer ◽  
Christopher J Donohoe

Quantifying the contribution of wild (naturally spawned) and hatchery Chinook salmon (Oncorhynchus tshawytscha) to the mixed-stock ocean fishery is critical to understanding their relative importance to the persistence of salmon stocks. The inability to distinguish hatchery and wild salmon has inhibited the detection of declines or recoveries for many wild populations. By using Chinook salmon of known hatchery and wild origin, we established a baseline for separating these two sources using otolith microstructure. Otoliths of wild salmon contained a distinct exogenous feeding check likely reflecting an abrupt transition in food resources from maternal yolk not experienced by fish reared in hatcheries. Daily growth increments in otoliths from hatchery salmon immediately after the onset of exogenous feeding were wider and more uniform in width than those in wild fish. The discriminant function that we used to distinguish individuals reared in hatcheries or in the wild was robust between years (1999 and 2002), life history stages (juveniles and adults), and geographic regions (California, British Columbia, and Alaska) and classified fish with ~91% accuracy. Results from our mixed-stock model estimated that the contribution of wild fish was 10% ± 6%, indicating hatchery supplementation may be playing a larger role in supporting the central California coastal fishery than previously assumed.


1995 ◽  
Vol 52 (2) ◽  
pp. 344-352 ◽  
Author(s):  
Z. Zhang ◽  
R. J. Beamish ◽  
B. E. Riddell

Otolith microstructure exhibited some characteristic differences between hatchery-reared and wild chinook salmon (Oncorhynchus tshawytscha) from the Cowichan River. Daily growth increments that formed in the otoliths of the hatchery-reared chinook salmon after exogenous feeding were more regular in width and contrast than those in the otoliths of wild chinook salmon. In addition, otoliths from hatchery-reared individuals frequently produced a check when the fish were released from the hatchery. Eighty-nine percent of a sample of 67 chinook smolts that had been coded-wire tagged in hatcheries and later captured in the Strait of Georgia were correctly identified as originating from hatcheries based on otolith microstructure. These tagged fish originated from at least 17 different hatcheries, indicating that the method could be used to identify chinook salmon originating from other hatcheries.


1982 ◽  
Vol 39 (7) ◽  
pp. 937-942 ◽  
Author(s):  
Steven E. Campana ◽  
John D. Neilson

Tetracycline injected into juvenile starry flounders (Platichthys stellatus) was incorporated into the periphery of the sagittal otoliths within 24 h. The resulting band, visible under ultraviolet light, was used as a dated mark on the otolith growth increments. This technique was used to verify that increments were laid down on a daily basis, both in field and laboratory environments. Subdaily increments were visible in otoliths of fishes reared under most environmental conditions. The production of daily increments in juvenile starry flounders preconditioned to a natural environmental regime was unaffected by photoperiod or temperature fluctuation, suggesting the presence of an internal circadian rhythm.Key words: starry flounder, Platichthys stellatus; otoliths, daily rings, growth increments, circadian, tetracycline


Author(s):  
Lia Chalifour ◽  
David C Scott ◽  
Misty MacDuffee ◽  
Steven Stark ◽  
John F Dower ◽  
...  

Estuaries represent a transition zone for salmon migrating from freshwater to marine waters, yet their contribution to juvenile growth is poorly quantified. Here, we use genetic stock identification and otolith analyses to quantify estuarine habitat use by Chinook salmon (<i>Oncorhynchus tshawytscha</i>) – the Pacific salmon species considered most reliant on this habitat – in Canada’s most productive salmon river, the Fraser. Two years of sampling revealed subyearling migrant (“ocean-type”) Chinook from the Harrison River to be the estuary’s dominant salmon population throughout the emigration period. These Chinook salmon were caught predominantly in the estuary’s brackish marshes but shifted to more saline habitats as they grew. Otolith analyses indicated that these Chinook salmon have wide-ranging entry timing (from February to May), and longer estuarine residency (weeks to months, mean 41.8 days) than estimated by prior studies, but similar daily growth rates (mean 0.57 mm +/- 0.13 SD) across entry dates and residency periods, implying sufficient foraging opportunities throughout the emigration period and habitats. Together, these results suggest that estuarine habitat is more important for early marine growth of subyearling migrant Chinook salmon than previously recognized.


1984 ◽  
Vol 62 (1) ◽  
pp. 65-71 ◽  
Author(s):  
L. M. Carl

Spawning density and the time of spawning (October) were similar in two tributaries of Lake Michigan in 1977 and 1978. Drift of recently emerged fry began in April and continued into June. During 1977–1979, the density of chinook salmon juveniles increased rapidly in early May to 0.3–2.9 fish/m2 and then declined to 0.2–0.8 fish/m2 by late June when most of the fish smolted. Instantaneous mortality estimates were variable between years and sites in both creeks, but overall mortality was similar in both streams with an average daily rate of 0.024 for Baldwin Creek and 0.025 for Pine Creek. A regression of the mortality rates versus initial density indicated the mortality rates were dependent on the initial fry density. There was no correlation between an index of spawner density and the number of smolts produced. No correlation was found between initial resident fry density and emergent fry colonization. Size-selective mortality was indicated in some stream sections. The daily growth rates for fish in both streams varied between 0.28 and 1.01 mm per day. These rates were similar to or higher than rates reported in the literature from other stocks of chinook salmon on the west coast of North America and Lake Ontario.


1996 ◽  
Vol 47 (2) ◽  
pp. 273 ◽  
Author(s):  
IM Suthers

In February 1993, the pelagic juvenile myctophid Diaphus kapalae was sampled with a neuston net in the southern Coral Sea in a region of flow disturbance north of Cato Reef, and to the east in the free stream (northerly flow at 30 cm s-1). There was no significant difference in the size (11-16 mm SL) or age (45-74 days after hatching) between the two regions. Recent growth indices derived from the width of the peripheral daily growth increments (~10 μm each) revealed enhanced otolith growth 38 km downstream and up to 4 days before capture. No significant difference was found for times longer than a week before capture, consistent with fluctuation of the wake indicated from current-meter data. Daily increment formation was confirmed by marginal increment analysis. Recent otolith growth was correlated with the RNA content adjusted by dry weight, which also revealed significantly higher condition in the wake region. Recent growth was correlated with microzooplankton biomass, recorded with an optical plankton counter.


2001 ◽  
Vol 58 (11) ◽  
pp. 2204-2212 ◽  
Author(s):  
P Pepin ◽  
J F Dower ◽  
H P Benoît

Patterns in increment widths and the associated measurement error were studied in the otoliths of radiated shanny (Ulvaria subbifurcata) larvae sampled from the field. Mean increment widths increased with larval age, whereas the relative measurement error decreased. Furthermore, the level of serial correlation in increment widths showed a clear increase with age. When measurement error was taken into consideration, the pattern of serial correlation indicates that an individual's growth increments did not show the effect of changes in local environmental conditions for at least 3 days, independent of age. Only after that period can we hope to detect the effect of environmental influences on increment widths (and by inference growth rates). The patterns of measurement error and serial correlation will have direct impacts on our ability to find the influence of environmental conditions on growth rates of individual larvae and determine patterns of selective loss in a population of larval fish.


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