scholarly journals How Dogs Domesticated

2018 ◽  
Author(s):  
Brian M Coyle

The dog, Canis familiaris, has classical domestication attributes, possibly derived from selection for tameness, except one: the capacity to share a long gaze (30+ seconds) with a human. All dog breeds have this capacity, even puppies prior to human socialization. No other domesticate can do so. Only Great Apes, among over 5000 mammals, can. Shared gazing replaces cortisol-based fight/flight hormone response with an oxytocin governed phobia/philia response. It involves mutations in neural hormone receptors, iris visibility, periorbital muscle control, and mate selection. Shared gazing contradicts domestication induced adolescent behavior fixation, as it requires apparent cognitive control of distractions. Domestication usually amplifies and suppresses existing traits. Humans still cannot induce complex beneficial mutations in animals. Therefore shared gazing likely evolved prior to domestication. Recent genomics evidence, comparing contemporary dogs and other canids, as well as sequencing archaeological canid remains, pushes back dog origins between 20,000 and 200,000 years BP. No evidence of human domestication efforts exists prior to 15,000 years BP. I review the genetic, archaeological, and experimental evidence of dog origins, which reveal tension in a dominant explanatory paradigm. Many researchers assume dogs evolved only through artificial selection. Evidence of ancient origins requires positing a far more ancient domestication activity than seems reasonable, or else reframing (or dismissing) evidence. Neither is necessary if 1) dogs evolved prior to domestication, 2) this pre-domesticated canid had a shared-gaze capacity, and 3) during the period of hunter-gatherer population increase, this capacity was exploited because it helped humans develop emotional attachment skills. Hunter-gatherer reports suggests the shared-gaze is key to canid domestication. Others have suggested this dog capacity might be a factor in their domestication. This paper's hypothesis makes it central to the process.

Genetics ◽  
2013 ◽  
Vol 196 (3) ◽  
pp. 829-840 ◽  
Author(s):  
Timothy M. Beissinger ◽  
Candice N. Hirsch ◽  
Brieanne Vaillancourt ◽  
Shweta Deshpande ◽  
Kerrie Barry ◽  
...  

2006 ◽  
Vol 35 ◽  
pp. 247-250
Author(s):  
H. Randle ◽  
E. Elworthy

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).


2011 ◽  
Vol 300 (4) ◽  
pp. R835-R843 ◽  
Author(s):  
Donato A. Rivas ◽  
Sarah J. Lessard ◽  
Misato Saito ◽  
Anna M. Friedhuber ◽  
Lauren G. Koch ◽  
...  

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.


Genetics ◽  
1980 ◽  
Vol 94 (4) ◽  
pp. 989-1000
Author(s):  
Francis Minvielle

ABSTRACT A quantitative character controlled at one locus with two alleles was submitted to artificial (mass) selection and to three modes of opposing natural selection (directional selection, overdominance and underdominance) in a large random-mating population. The selection response and the limits of the selective process were studied by deterministic simulation. The lifetime of the process was generally between 20 and 100 generations and did not appear to depend on the mode of natural selection. However, depending on the values of the parameters (initial gene frequency, selection intensity, ratio of the effect of the gene to the environmental standard deviation, fitness values) the following outcomes of selection were observed: fixation of the allele favored by artificial selection, stable nontrivial equilibrium, unstable equilibrium and loss of the allele favored by artificial selection. Finally, the results of the simulation were compared to the results of selection experiments.


2012 ◽  
Vol 26 (S1) ◽  
Author(s):  
Sira Maria Torvinen ◽  
Mika Silvennoinen ◽  
Maria Mikkonen ◽  
Lauren G. Koch ◽  
Steven L. Britton ◽  
...  

2008 ◽  
Vol 2 (2) ◽  
pp. 172-186 ◽  
Author(s):  
Lesley G. Campbell ◽  
Allison A. Snow ◽  
Patricia M. Sweeney ◽  
Julie M. Ketner

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