Physiological and Behavioral Consequences of Long‐Term Artificial Selection for Vulnerability to Recreational Angling in a Teleost Fish

2007 ◽  
Vol 80 (5) ◽  
pp. 480-490 ◽  
Author(s):  
Steven J. Cooke ◽  
Cory D. Suski ◽  
Kenneth G. Ostrand ◽  
David H. Wahl ◽  
David P. Philipp
Keyword(s):  
Artificial Selection ◽  
Teleost Fish ◽  
Behavioral Consequences ◽  
Recreational Angling ◽  
Selection For

scholarly journals A Genome-Wide Scan for Evidence of Selection in a Maize Population Under Long-Term Artificial Selection for Ear Number

Genetics ◽  
2013 ◽  
Vol 196 (3) ◽  
pp. 829-840 ◽  
Author(s):  
Timothy M. Beissinger ◽  
Candice N. Hirsch ◽  
Brieanne Vaillancourt ◽  
Shweta Deshpande ◽  
Kerrie Barry ◽  
...  
Keyword(s):  
Artificial Selection ◽  
Maize Population ◽  
Genome Wide ◽  
A Genome ◽  
Selection For ◽  
Ear Number ◽  
Genome Wide Scan

scholarly journals The Genetic Architecture of Response to Long-Term Artificial Selection for Oil Concentration in the Maize Kernel

Genetics ◽  
2004 ◽  
Vol 168 (4) ◽  
pp. 2141-2155 ◽  
Author(s):  
Cathy C. Laurie ◽  
Scott D. Chasalow ◽  
John R. LeDeaux ◽  
Robert McCarroll ◽  
David Bush ◽  
...  
Keyword(s):  
Artificial Selection ◽  
Genetic Architecture ◽  
Maize Kernel ◽  
Oil Concentration ◽  
Selection For

The relationship between facial whorl direction and sidedness in ridden horses

2006 ◽  
Vol 35 ◽  
pp. 247-250
Author(s):  
H. Randle ◽  
E. Elworthy
Keyword(s):  
Natural Selection ◽  
Artificial Selection ◽  
Competitive Ability ◽  
Close Association ◽  
Human Behaviour ◽  
Physical Ability ◽  
Facial Hair ◽  
Selection For ◽  
The Relationship ◽  
The Brain

The influence of Natural Selection on the evolution of the horse (Equus callabus) is minimal due to its close association with humans. Instead Artificial Selection is commonly imposed through selection for features such as a ‘breed standard’ or competitive ability. It has long been considered to be useful if indicators of characteristics such as physical ability could be identified. Kidd (1902) suggested that the hair coverings of animals were closely related to their lifestyle, whether they were active or passive. In 1973 Smith and Gong concluded that hair whorl (trichloglyph) pattern and human behaviour is linked since hair patterning is determined at the same time as the brain develops in the foetus. More recently Grandin et al. (1995), Randle (1998) and Lanier et al. (2001) linked features of facial hair whorls to behaviour and production in cattle. Hair whorl features have also been related to temperament in equines (Randle et al., 2003).

scholarly journals Low intrinsic running capacity is associated with reduced skeletal muscle substrate oxidation and lower mitochondrial content in white skeletal muscle

2011 ◽  
Vol 300 (4) ◽  
pp. R835-R843 ◽  
Author(s):  
Donato A. Rivas ◽  
Sarah J. Lessard ◽  
Misato Saito ◽  
Anna M. Friedhuber ◽  
Lauren G. Koch ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Insulin Sensitivity ◽  
Aerobic Capacity ◽  
Artificial Selection ◽  
White Muscle ◽  
Metabolic Diseases ◽  
Metabolic Health ◽  
Mitochondrial Content ◽  
Red Muscle ◽  
Selection For

Chronic metabolic diseases develop from the complex interaction of environmental and genetic factors, although the extent to which each contributes to these disorders is unknown. Here, we test the hypothesis that artificial selection for low intrinsic aerobic running capacity is associated with reduced skeletal muscle metabolism and impaired metabolic health. Rat models for low- (LCR) and high- (HCR) intrinsic running capacity were derived from genetically heterogeneous N:NIH stock for 20 generations. Artificial selection produced a 530% difference in running capacity between LCR/HCR, which was associated with significant functional differences in glucose and lipid handling by skeletal muscle, as assessed by hindlimb perfusion. LCR had reduced rates of skeletal muscle glucose uptake (∼30%; P = 0.04), glucose oxidation (∼50%; P = 0.04), and lipid oxidation (∼40%; P = 0.02). Artificial selection for low aerobic capacity was also linked with reduced molecular signaling, decreased muscle glycogen, and triglyceride storage, and a lower mitochondrial content in skeletal muscle, with the most profound changes to these parameters evident in white rather than red muscle. We show that a low intrinsic aerobic running capacity confers reduced insulin sensitivity in skeletal muscle and is associated with impaired markers of metabolic health compared with high intrinsic running capacity. Furthermore, selection for high running capacity, in the absence of exercise training, endows increased skeletal muscle insulin sensitivity and oxidative capacity in specifically white muscle rather than red muscle. These data provide evidence that differences in white muscle may have a role in the divergent aerobic capacity observed in this generation of LCR/HCR.

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