scholarly journals Sentinel California sea lions provide insight into legacy organochlorine exposure trends and their association with cancer and infectious disease

One Health ◽  
2015 ◽  
Vol 1 ◽  
pp. 37-43 ◽  
Author(s):  
Nistara Randhawa ◽  
Frances Gulland ◽  
Gina M. Ylitalo ◽  
Robert DeLong ◽  
Jonna A.K. Mazet
2005 ◽  
Vol 5 (1) ◽  
pp. 140-142 ◽  
Author(s):  
F. D. HERNANDEZ-VELAZQUEZ ◽  
C. E. GALINDO-SANCHEZ ◽  
M. I. TAYLOR ◽  
J. DE LA ROSA-VELEZ ◽  
I. M. COTE ◽  
...  

2001 ◽  
Vol 79 (6) ◽  
pp. 1080-1087 ◽  
Author(s):  
Anthony J Orr ◽  
James T Harvey

The purpose of this study was to quantify the errors associated with using fecal samples to determine the diet of the California sea lion (Zalophus californianus). Fishes and squids of known size and number were fed to five sea lions held in enclosures with seawater-filled pools. Enclosures were washed and pools were drained periodically so that sea lion feces could be collected using a 0.5 mm mesh bag. Fish otoliths and squid beaks were collected from feces and used to estimate number and size of prey eaten. An average of 50.7% (SE = 6.4%) of 430 fishes and 73.5% (SE = 12.0%) of 49 cephalopods fed to sea lions were represented by otoliths and beaks in feces, respectively. Estimated lengths of fish from feces were less than lengths of fish fed to sea lions by an average of 30.1% (SE = 2.8%). Beaks were not digested significantly; estimated lengths of squid were underestimated by an average of only 3.3% (SE = 1.5%) relative to actual lengths. Passage rates of otoliths varied, but more than 70% were recovered within 48 h after the fish was consumed. Passage rates of beaks were generally less than those of otoliths; six beaks (11%) were collected in feces 4 days after the squid were eaten. Correction factors were created to more reliably estimate the number and size of fishes and cephalopods eaten by California sea lions.


AJIL Unbound ◽  
2017 ◽  
Vol 111 ◽  
pp. 272-276
Author(s):  
Jérôme de Hemptinne

In times of war, the first instinct is to relieve the suffering of human beings. Environmental and animal interests are always pushed into the background. However, warfare strongly affects natural resources, including animals, which makes animal issues a matter of great concern. Certain species have been vanishing at a rapid rate because of wars, often with disastrous effects on the food chain and on the ecological balance. Indeed, belligerents rarely take into account the adverse consequences of their military operations on animals. They even take advantage of the chaotic circumstances of war in order to poach protected species and to engage in the trafficking of expensive animal products. While generating billions of dollars each year, such poaching and trafficking allows armed groups to grow and to reinforce their authority over disputed territory. States have also trained, and continue to train, certain animals—principally marine mammals such as bottlenose dolphins and California sea lions—to perform military tasks, like ship and harbor protection, or mine detection and clearance. Millions of horses, mules, donkeys, camels, dogs, and birds are obliged to serve on various fronts (transport, logistics, or communications) and become particularly vulnerable targets.


1974 ◽  
Vol 10 (4) ◽  
pp. 370-376 ◽  
Author(s):  
J. C. SWEENEY ◽  
W. G. GILMARTIN

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.


2018 ◽  
Vol 54 (3) ◽  
pp. 581-586 ◽  
Author(s):  
Alissa C. Deming ◽  
Kathleen M. Colegrove ◽  
Padraig J. Duignan ◽  
Ailsa J. Hall ◽  
James F. X. Wellehan ◽  
...  

2004 ◽  
Vol 131 (3) ◽  
pp. 425-434 ◽  
Author(s):  
K Kannan ◽  
N Kajiwara ◽  
B.J Le Boeuf ◽  
S Tanabe

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