Reassessment of spiny dogfish Squalus acanthias age and growth using vertebrae and dorsal-fin spines

2011 ◽  
Vol 80 (5) ◽  
pp. 1300-1319 ◽  
Author(s):  
W. J. Bubley ◽  
J. Kneebone ◽  
J. A. Sulikowski ◽  
P. C. W. Tsang
2021 ◽  
Vol 119 (1) ◽  
pp. 41-49
Author(s):  
Kelsey C. James ◽  
Lisa J. Natanson ◽  
Christopher Flight ◽  
Cindy Tribuzio ◽  
John Hoey ◽  
...  

2018 ◽  
Vol 69 (1) ◽  
pp. 37 ◽  
Author(s):  
Cindy A. Tribuzio ◽  
Mary Elizabeth Matta ◽  
Christopher Gburski ◽  
Calvin Blood ◽  
Walter Bubley ◽  
...  

Historically, Pacific spiny dogfish (Squalus suckleyi) have been aged using dorsal fin spines, a method that was validated through bomb radiocarbon analysis and oxytetracycline tagging. However, ages generated using this method generally have poor precision and require estimation of missing growth bands in eroded spines, prompting a search for improved age determination methods. In the present study, spiny dogfish were aged using the historical spine method and a new method involving stained thin sections of vertebral centra. Results of an inter-laboratory exchange demonstrated the need for readers to calibrate ageing criteria with a reference collection before reading structures, a practice that yielded significant improvements in between-reader precision of spine band pair counts. After calibration, the primary readers examined the full sample set. The two structures yielded similar age estimates for younger animals, but centrum estimates were consistently younger than spine estimates after age-10. Although further work is necessary to fully explore potential reasons for the observed bias, such as centrum size and location within the vertebral column, at the present time centra are not a suitable alternative to dorsal fin spines for age determination of Pacific spiny dogfish >10 years of age.


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


2004 ◽  
Vol 13 (1) ◽  
pp. 117-119
Author(s):  
A.M. Prokofiev

Capros longispinatus kelasuriensis subsp. n. is described from the Upper Subhorizon of Morozkina Balka (basal part of the Upper Oligocene) of Abkhazia. It precedes stratigraphically the nominotypical subspecies and differs from the latter chiefly in the much shorter dorsal-fin spines.


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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