Daily Growth Increments in Otoliths of Starry Flounder (Platichthys stellatus) and the Influence of Some Environmental Variables in Their Production

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


1983 ◽  
Vol 61 (7) ◽  
pp. 1591-1597 ◽  
Author(s):  
Steven E. Campana

Juvenile steelhead trout (Salmo gairdneri) and starry flounders (Platichthys stellatus) were reared 64–76 days under various experimental feeding regimes to determine if feeding periodicity influenced the production of daily growth increments on the otoliths. Both species produced daily increments when fed thrice daily, daily, or once every 3 days, as well as through 26–32 days of starvation. Daily growth increments were also deposited in vateritic ("crystalline") otoliths, which constituted 27% of the trout sagittae sampled. Feeding frequency affected increment appearance and the incidence of subdaily increments in trout, but not in flounders. The difference in effect was probably due to the higher metabolic rate of trout. Increment deposition in all flounders was far more variable than in trout, and some flounders apparently ceased increment formation altogether.





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



1968 ◽  
Vol 42 (S2) ◽  
pp. 64-80 ◽  
Author(s):  
Giorgio Pannella ◽  
Copeland Macclintock

Tidal cycles are reflected in daily growth-increment sequences in shells of many Recent and fossil mollusks. Living specimens of the bivalve Mercenaria mercenaria were notched at the growing edge of the shell and planted intertidally in Barnstable Harbor, Massachusetts. Shells from two lots, killed at intervals of 368 and 723 days after planting, show the same number of small growth increments as there were days from notching to killing. Superimposed on daily growth record are effects of winter (thin daily increments) and tides (14-day cycles of thick and thin daily increments). Comparison of Barnstable tide record with the first year's growth shows that, for each 14-day cycle, thin daily increments form during neap tides and thicker daily increments form during spring tides. Although tidal patterns are present in subtidal Mercenaria shells, they are rarely as pronounced as in intertidal ones. Spawning patterns differ from winter patterns; they are expressed in the shell by an interruption of regular deposition followed by a series of thin daily increments. Continuous sequences of bidaily patterns, one thick daily increment followed by a relatively thin one, are common in M. mercenaria.The clearest 14-day cycles of deposition were seen in shells of the bivalve Tridacna squamosa. Each daily neap-tide increment is a simple layer consisting of a dark and light zone. Each daily spring-tide increment is a complex layer consisting of two light-dark alternations separated by a depositional break that is more pronounced than the breaks delimiting daily intervals. Preliminary results of growth-increment counts in fossils show a generally decreasing trend of the mean values of days per lunar month toward the Recent. The Pennsylvanian value is 30.07 ± 0.08, a figure that is in general agreement with those of Scrutton (1964), who counted 30.59 days per month on Devonian corals, and Barker (1966), who reported more than 30 days per month in Pennsylvanian bivalves.



1982 ◽  
Vol 39 (10) ◽  
pp. 1335-1339 ◽  
Author(s):  
Kenneth H. Wilson ◽  
P. A. Larkin

Sixty-four laboratory-reared sockeye salmon (Oncorhynchus nerka) fry were marked to enable identification as individuals. Each was weighed initially on June 6 or 8, 1979; and again on July 6; and surviving fish were weighed a third time on July 20. After the final weighing, sagittae were removed and a standard otolith radius, corresponding to each weight, was determined by counting back from the otolith edge the appropriate number of daily increments. The regression of ln otolith radius on ln fish weight was linear, with r2 = 0.92, demonstrating a relationship between mean thickness of a daily increment in sagittae, and mean daily change in weight of the fry. Using this regression line, previous weights were back calculated from corresponding otolith radii with errors in the order of 15%.Key words: otoliths, daily growth increments, back calculation, sockeye salmon



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.



1976 ◽  
Vol 33 (11) ◽  
pp. 2577-2586 ◽  
Author(s):  
S. R. Wellings ◽  
C. E. Alpers ◽  
B. B. McCain ◽  
B. S. Miller

Fin erosion in the starry flounder (Platichthys stellatus) and English sole (Parophrys vetulus) of the Duwamish River, Washington, is characterized by ulcerating chronic inflammation and fibrosis with resorption of fin rays. The end result is deformation, shortening, and retraction of residual fin tissue with loss of functional surface. We suggest that the incidence of fin erosion in a particular population is related to an interaction between genetic constitution and multiple environmental variables, including a variety of chemical pollutants.



2004 ◽  
Vol 55 (4) ◽  
pp. 403 ◽  
Author(s):  
Mitsuo Sakai ◽  
Norma Brunetti ◽  
Marcela Ivanovic ◽  
Beatriz Elena ◽  
Kazuyoshi Nakamura

To identify sub-daily or aperiodic increments of statolith growth in the ommastrephid squid Illex argentinus, we examined statolith microstructure, especially with regard to the natal ring, where counting of daily growth increments should begin, and the widths of subsequent daily increments. Paralarvae obtained by artificial fertilisation were incubated on board at different temperatures ranging from 11.4 to 25.4°C, and were starved throughout the experiments. We observed statolith growth from newly hatched to 10-day-old paralarvae and used alizarine complexone staining to attempt validation of the growth. The maximum statolith radius (MSR) of newly hatched paralarvae was constant at 21.1 μm across the full range of temperatures, with the exception of 25.4°C. Daily growth of MSR was analysed separately in two phases, the pre-yolk-absorption phase (i.e. yolk sac still present) and the post-yolk-absorption phase. During the pre-yolk-absorption phase, the daily growth rate (DGR, y) of the MSR varied from 3 to 7 μm day–1 depending on rearing temperature (x) and was expressed as y = 0.37x – 1.77. We concluded that the natal ring forms at 21 μm MSR. The initial increment width obtained from the DGR of MSR seems applicable for distinguishing daily rings from sub-daily rings, although this application should be limited to hatchling paralarvae in the pre-yolk-absorption phase.



2019 ◽  
Vol 7 (1) ◽  
Author(s):  
Natalie V. Klinard ◽  
Edmund A. Halfyard ◽  
Jordan K. Matley ◽  
Aaron T. Fisk ◽  
Timothy B. Johnson

Abstract Background Acoustic telemetry is an increasingly common method used to address ecological questions about the movement, behaviour, and survival of freshwater and marine organisms. The variable performance of acoustic telemetry equipment and ability of receivers to detect signals from transmitters have been well studied in marine and coral reef environments to inform study design and improve data interpretation. Despite the growing use of acoustic telemetry in large, deep, freshwater systems, detection efficiency and range, particularly in relation to environmental variation, are poorly understood. We used an array of 90 69-kHz acoustic receivers and 8 sentinel range transmitters of varying power output deployed at different depths and locations approximately 100–9500 m apart for 215 days to evaluate how the detection efficiency of acoustic receivers varied spatially and temporally in relation to environmental conditions. Results The maximum distance that tags were detected ranged from 5.9 to 9.3 km. Shallow tags consistently had lower detection efficiency than deep tags of the same power output and detection efficiency declined through the winter months (December–February) of the study. In addition to the distance between tag and receiver, thermocline strength, surface water velocity, ice thickness, water temperature, depth range between tag and receiver, and number of fish detections contributed to explaining variation in detection efficiency throughout the study period. Furthermore, the most significant models incorporated interactions between several environmental variables and tag–receiver distance, demonstrating the complex temporal and spatial relationships that exist in heterogeneous environments. Conclusions Relying on individual environmental variables in isolation to interpret receiver performance, and thus animal behaviour, may be erroneous when detection efficiency varies across distances, depths, or tag types. As acoustic telemetry becomes more widely used to study ecology and inform management, it is crucial to understand its limitations in heterogeneous environments, such as freshwater lakes, to improve the quality and interpretation of data. We recommend that in situ range testing and retrospective analysis of detection efficiency be incorporated into study design for telemetry projects. Furthermore, we caution against oversimplifying the dynamic relationship between detection efficiency and environmental conditions for the sake of producing a correction that can be applied directly to detection data of tagged animals when the intended correction may not be justified.



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