Eye lens aging in the spiny dogfish (Squalus acanthias) I. Age determination from lens weight

1989 ◽  
Vol 8 (7) ◽  
pp. 707-712 ◽  
Author(s):  
Roland J. Siezen
2021 ◽  
Vol 119 (1) ◽  
pp. 41-49
Author(s):  
Kelsey C. James ◽  
Lisa J. Natanson ◽  
Christopher Flight ◽  
Cindy Tribuzio ◽  
John Hoey ◽  
...  

1985 ◽  
Vol 42 (11) ◽  
pp. 1799-1805 ◽  
Author(s):  
Richard J. Beamish ◽  
Gordon A. McFarlane

Annual marks were visible in three different areas of the dogfish (Squalus acanthias) spine. The annuli in the mantle, the stem base, and the inner dentine develop independently of each other. Annuli that formed on the mantle were readily identifiable externally, making them the most useful for age determination. The mantle annulus is an accumulation of pigment that appears to form because enamel deposition is not synchronous with the upward growth of the spine, resulting in the production of darkened bands that often form ridges. We validated our interpretation of annuli from fish aged 20–70 yr by tagging and recovering dogfish that were injected with oxytetracycline. Through validation we were able to demonstrate that some previous studies have underestimated age, resulting in a misunderstanding of important life history parameters.


1977 ◽  
Vol 34 (1) ◽  
pp. 44-48 ◽  
Author(s):  
Barry C. Jones ◽  
Glen H. Geen

Ages of spiny dogfish (Squalus acanthias) in the Strait of Georgia, B.C., have been estimated by an X-ray spectrometric technique which involves measuring variations in the element composition within vertebrae.


1988 ◽  
Vol 46 (1) ◽  
pp. 81-93 ◽  
Author(s):  
Roland J. Siezen ◽  
Christine Hom ◽  
Elizabeth D. Kaplan ◽  
John A. Thomson ◽  
George B. Benedek

1978 ◽  
Vol 35 (6) ◽  
pp. 816-821 ◽  
Author(s):  
J. R. Brett ◽  
J. M. Blackburn

The metabolic rate of spiny dogfish, Squalus acanthias, was determined in both a tunnel respirometer and a large, covered, circular tank (mass respirometer). Swimming performance was very poor in the respirometer, so that a power–performance curve could not be established. Instead, resting metabolic rates were determined, with higher rates induced by causing heavy thrashing (active metabolism). Routine metabolic rates were measured for the spontaneous activity characterizing behavior in the circular tank. For fish of 2 kg mean weight, the metabolic rates at 10 °C were 32.4 ± 2.6 SE (resting), 49.2 ± 5.0 SE (routine), and 88.4 ± 4.6 SE (active) mg O2∙kg−1∙h−1. Assuming that the routine rate represents a general energy expenditure in nature, this is equivalent to metabolizing about 3.8 kcal∙kg−1∙d−1 (15.9 × 103 J∙kg−1∙d−1). Key words: dogfish, metabolic rates, energetics, respiration


2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Michael D. Ford ◽  
Jason S. Link

Previous descriptions have noted that the stomach samples of spiny dogfish, Squalus acanthias, showed a major increase in the overall occurrence and hence implied abundance of Ctenophora. This apparent and persistent gelatinous zooplankton outbreak is increasingly more common in the world’s oceans. We briefly explore the energetic ramifications of ctenophores in the spiny dogfish diet, inferring that the presence of gelatinous zooplankton represents an ambient feeding strategy. Relative to other prey, ctenophores are not a high energy density prey item. However, given varying assumptions of the amount of ctenophores consumed, they may be an important staple in the diet of spiny dogfish. We also examine the utility of using spiny dogfish as a gelatinous zooplankton sampling device. Using five calculation methodologies, we provide bounds on potential abundance and biomass estimates of ctenophores in the Northeast U.S. shelf ecosystem. We then contextualize these findings relative to the implications for the Northeast U.S. and any large marine ecosystem.


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