Spatial variation of heat flux in Steller sea lions: evidence for consistent avenues of heat exchange along the body trunk

2005 ◽  
Vol 315 (2) ◽  
pp. 163-175 ◽  
Author(s):  
Kate Willis ◽  
Markus Horning ◽  
David A.S. Rosen ◽  
Andrew W. Trites
Keyword(s):  
Heat Flux ◽  
Heat Exchange ◽  
Spatial Variation ◽  
The Body ◽  
Steller Sea Lions ◽  
Sea Lions

Hydrodynamic drag in steller sea lions (Eumetopias jubatus)

2000 ◽  
Vol 203 (12) ◽  
pp. 1915-1923 ◽  
Author(s):  
L.L. Stelle ◽  
R.W. Blake ◽  
A.W. Trites
Keyword(s):  
Minimum Cost ◽  
The Body ◽  
Hydrodynamic Drag ◽  
Eumetopias Jubatus ◽  
Steller Sea Lions ◽  
California Sea Lions ◽  
Cost Of Transport ◽  
Sea Lions ◽  
Drag Forces ◽  
The Individual

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.

Heat flux transducer measurement error: a simplified view

1993 ◽  
Vol 74 (4) ◽  
pp. 2040-2044 ◽  
Author(s):  
J. Frim ◽  
M. B. Ducharme
Keyword(s):  
Heat Flux ◽  
Heat Exchange ◽  
Measurement Error ◽  
Correction Factor ◽  
Theoretical Basis ◽  
The Body ◽  
Body Tissues ◽  
Small Correction ◽  
Precision Temperature ◽  
Body Heat

Heat flux transducers (HFTs) provide a simple and direct measurement of body heat exchange. Regrettably, HFTs perturb the heat flux at the measurement site, resulting in underestimations of the true heat flux. Equations to correct the discrepancy are available, but most require high-precision temperature measurements above and/or below the transducer and/or deep within the body tissues. Because this is not always feasible, the equations are of limited practical benefit. A theoretical basis for the magnitude of the correction factor in relation to the thermal resistances of the materials both above and below the HFT has been developed and has been verified experimentally. The theory is presented in a graph that can be used to drive the HFT correction factor directly or as a guide to know that heat flux was measured within a certain accuracy. This may obviate the use of complicated procedures and equations to perhaps needlessly apply a small correction factor to HFT data.

scholarly journals Cohort effects and spatial variation in age-specific survival of Steller sea lions from southeastern Alaska

Ecosphere ◽  
2011 ◽  
Vol 2 (10) ◽  
pp. art111 ◽  
Author(s):  
K. K. Hastings ◽  
L. A. Jemison ◽  
T. S. Gelatt ◽  
J. L. Laake ◽  
G. W. Pendleton ◽  
...  
Keyword(s):  
Spatial Variation ◽  
Cohort Effects ◽  
Steller Sea Lions ◽  
Sea Lions

Weighing our measures: approach-appropriate modeling of body composition in juvenile Steller sea lions (Eumetopias jubatus)

2015 ◽  
Vol 93 (3) ◽  
pp. 177-180 ◽  
Author(s):  
C.R. Shuert ◽  
J.P. Skinner ◽  
J.E. Mellish
Keyword(s):  
Body Composition ◽  
Body Condition ◽  
Small Sample ◽  
The Body ◽  
Lateral Side ◽  
Eumetopias Jubatus ◽  
Steller Sea Lions ◽  
Sea Lions ◽  
Development Framework ◽  
Total Body

While many approaches to modeling body condition exist, ranging from arbitrary morphometric indices to sophisticated cone modeling, few approaches have attempted to develop a standardized, simplified method for determining total body fat and protein in otariids. Our goal was to develop a method for predicting the body condition of juvenile Steller sea lions (Eumetopias jubatus (Schreber, 1776)) using simple morphometrics such as measurements of girth, length, mass, and blubber depth. We compared a candidate set of models to determine which metrics best predicted total body water (TBW) measures obtained by deuterium isotope dilution. Furthermore, we used AICc (Akaike’s information criterion corrected for small sample size) model selection methods and cross-validation to choose and validate the best suite of predictors. TBW was best predicted by a model that included mass, standard length, axial girth with the addition of blubber depths on the lateral side of the neck and dorsal surface of the hip. The results presented here show that blubber depth is an important addition to modeling body composition and may improve upon nonlethal, population-level estimates of nonisotopically derived values of TBW in juvenile Steller sea lions. Additionally, our models present a model development framework for other research efforts for use in determining body condition in otariids.

Diet composition of Steller sea lions (Eumetopias jubatus) in Frederick Sound, southeast Alaska: a comparison of quantification methods using scats to describe temporal and spatial variabilities

2015 ◽  
Vol 93 (5) ◽  
pp. 361-376 ◽  
Author(s):  
D.J. Tollit ◽  
M.A. Wong ◽  
A.W. Trites
Keyword(s):  
Pacific Salmon ◽  
Biomass Energy ◽  
Eumetopias Jubatus ◽  
Steller Sea Lions ◽  
Southeast Alaska ◽  
Merluccius Productus ◽  
Sea Lions ◽  
Sampling Protocols ◽  
Dietary Indices

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.

Maternal attendance patterns of Steller sea lions (Eumetopias jubatus) from stable and declining populations in Alaska

2003 ◽  
Vol 81 (2) ◽  
pp. 340-348 ◽  
Author(s):  
Linda L Milette ◽  
Andrew W Trites
Keyword(s):  
Prey Availability ◽  
A Priori ◽  
Population Decline ◽  
Perinatal Period ◽  
Eumetopias Jubatus ◽  
Steller Sea Lions ◽  
Sea Lions ◽  
First Feeding ◽  
Attendance Patterns ◽  
The Mean

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.

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