Three-dimensional photogrammetry as a tool for estimating morphometrics and body mass of Steller sea lions (Eumetopias jubatus)

2007 ◽  
Vol 64 (2) ◽  
pp. 296-303 ◽  
Author(s):  
Jason N Waite ◽  
Wendy J Schrader ◽  
Jo-Ann E Mellish ◽  
Markus Horning

A technique was developed to estimate morphometrics and body mass of Steller sea lions (Eumetopias jubatus) using three-dimensional (3D) photogrammetry. 3D photogrammetry reduces many of the problems associated with camera and body position encountered with two-dimensional photogrammetric techniques, allowing body mass estimation of free-ranging, active sea lions, without sedation, heavy weighing equipment, and disturbance. 3D computer wireframes of 53 Steller sea lions of various age classes were generated from multiple time-synchronous digital photos and used to estimate length, girth, and volume. Average estimates of standard length and axillary girth were within ±2.5% and ±4.0% of physically measured dimensions, respectively. Average estimates of standard length and axillary girth using only wireframes based on ideal body postures were within ±1.7% and ±3.1% of physically measured dimensions, respectively. Regressions of physically measured mass on photogrammetrically estimated body volume yielded a predictive model. Body mass estimates using this model were on average within 9.0% (95% confidence interval = ±1.7%) of the physically measured mass. This technique was also successfully applied to reptiles and fish.

2000 ◽  
Vol 78 (7) ◽  
pp. 1243-1250 ◽  
Author(s):  
David AS Rosen ◽  
Andrew W Trites

The decline of Steller sea lions (Eumetopias jubatus) in the Gulf of Alaska and the Aleutian Islands may be the result of them eating too much pollock (a gadid fish) instead of a more balanced and diverse diet containing fattier fishes, such as herring or sandlance. We sought to test this junk-food hypothesis by feeding six captive Steller sea lions (ages 0.9-4.5 years) only pollock or herring. All sea lions gained mass while eating herring. However, eating only pollock for short periods (11-23 d) caused the study animals to lose an average of 6.5% of their initial body mass (0.6 kg/d) over an average feeding trial of 16 d (initial mass averaged 125 kg). The animals were allowed to eat as much pollock as they wanted but did not increase their food intake to compensate for the low energy they were receiving. The sea lions showed progressive metabolic depression while losing body mass on a pollock-only diet. The loss of body mass while eating pollock was due to the lower gross energy content of pollock versus herring, the higher cost of digesting pollock, and the increased energy loss from digesting the larger quantity of fish needed to compensate for the lower energy content of pollock. Thus, our sea lions would have had to eat 35-80% more pollock than herring to maintain similar net energy intakes. Results from our captive-feeding studies are consistent with the junk-food hypothesis and have serious implications for Steller sea lions that have been eating primarily pollock in the Gulf of Alaska and the Aleutian Islands.


2015 ◽  
Vol 93 (5) ◽  
pp. 361-376 ◽  
Author(s):  
D.J. Tollit ◽  
M.A. Wong ◽  
A.W. Trites

We compared eight dietary indices used to describe the diet of Steller sea lions (Eumetopias jubatus (Schreber, 1776)) from 2001 to 2004 in Frederick Sound, southeast Alaska. Remains (n = 9666 items) from 59+ species categories were identified from 1684 fecal samples (scats) from 14 collection periods. The most frequently occurring prey were walleye pollock (Theragra chalcogramma (Pallas, 1814) = Gadus chalcogrammus Pallas, 1814; 95%), Pacific herring (Clupea pallasii Valenciennes in Cuvier and Valenciennes, 1847; 30%), Pacific hake (Merluccius productus (Ayres, 1855); 29%), and arrowtooth flounder (Atheresthes stomias (Jordan and Gilbert, 1880) = Reinhardtius stomias (Jordan and Gilbert, 1880); 21%). These species, along with Pacific salmon (genus Oncorhynchus Suckley, 1861) and skate (genus Raja L., 1758), accounted for 80%–90% of the reconstructed biomass and energy contribution, with pollock contributing 37%–60%. Overall, 80% of fish were 14–42 cm long and mainly pelagic, though 40% of scats contained benthic-associated prey. Steller sea lions switched from adult pollock to strong cohorts of juvenile pollock, and took advantage of spawning concentrations of salmon in autumn and herring in late spring and summer, as well as a climate-driven increase in hake availability. Observed temporal and site differences in diet confirm the need for robust long-term scat sampling protocols. All major indices similarly tracked key temporal changes, despite differences in occurrence and biomass-energy-based diet estimates linked to prey size and energy-density effects and the application of correction factors.


2003 ◽  
Vol 81 (2) ◽  
pp. 340-348 ◽  
Author(s):  
Linda L Milette ◽  
Andrew W Trites

Maternal attendance patterns of Alaskan Steller sea lions (Eumetopias jubatus) were compared during the summer breeding seasons in 1994 and 1995 at Sugarloaf Island (a declining population) and Lowrie Island (a stable population). Our goal was to determine whether there were differences in maternal attendance between the two populations that were consistent with the hypothesis that lactating Steller sea lions in the area of decline were food-limited during summer. Our a priori expectations were based on well-documented behavioural responses of otariids to reduced prey availability. We found that foraging trips were significantly shorter in the area of population decline, counter to initial predictions. The mean length of foraging trips in the declining area was 19.5 h compared with 24.9 h in the stable area. In contrast, the mean perinatal period (time between parturition and first feeding trip) was significantly longer in the area of decline (9.9 versus 7.9 days), again countering initial predictions. The mean length of shore visits for the declining population was also significantly longer (27.0 h compared with 22.6 h where the population was stable). For both populations, the mean time that mothers foraged increased as pups grew older, whereas the time that they spent on shore with their pups became shorter. Behavioural observations of maternal attendance patterns are inconsistent with the hypothesis that lactating Steller sea lions from the declining population had difficulty obtaining prey during summer.


2013 ◽  
Vol 183 (5) ◽  
pp. 699-708 ◽  
Author(s):  
Carling D. Gerlinsky ◽  
David A. S. Rosen ◽  
Andrew W. Trites

Mammal Study ◽  
2021 ◽  
Vol 46 (1) ◽  
Author(s):  
Kaoru Hattori ◽  
Toshihide Kitakado ◽  
Takeomi Isono ◽  
Orio Yamamura

2000 ◽  
Vol 203 (12) ◽  
pp. 1915-1923 ◽  
Author(s):  
L.L. Stelle ◽  
R.W. Blake ◽  
A.W. Trites

Drag forces acting on Steller sea lions (Eumetopias jubatus) were investigated from ‘deceleration during glide’ measurements. A total of 66 glides from six juvenile sea lions yielded a mean drag coefficient (referenced to total wetted surface area) of 0.0056 at a mean Reynolds number of 5.5×10(6). The drag values indicate that the boundary layer is largely turbulent for Steller sea lions swimming at these Reynolds numbers, which are past the point of expected transition from laminar to turbulent flow. The position of maximum thickness (at 34 % of the body length measured from the tip of the nose) was more anterior than for a ‘laminar’ profile, supporting the idea that there is little laminar flow. The Steller sea lions in our study were characterized by a mean fineness ratio of 5.55. Their streamlined shape helps to delay flow separation, reducing total drag. In addition, turbulent boundary layers are more stable than laminar ones. Thus, separation should occur further back on the animal. Steller sea lions are the largest of the otariids and swam faster than the smaller California sea lions (Zalophus californianus). The mean glide velocity of the individual Steller sea lions ranged from 2.9 to 3.4 m s(−)(1) or 1.2-1.5 body lengths s(−)(1). These length-specific speeds are close to the optimum swim velocity of 1.4 body lengths s(−)(1) based on the minimum cost of transport for California sea lions.


2009 ◽  
Vol 82 (3) ◽  
pp. 236-247 ◽  
Author(s):  
Lorrie D. Rea ◽  
Michelle Berman‐Kowalewski ◽  
David A. S. Rosen ◽  
Andrew W. Trites

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