scholarly journals A Brain Module for Scalable Control of Complex, Multi-motor Threat Displays

Neuron ◽  
2018 ◽  
Vol 100 (6) ◽  
pp. 1474-1490.e4 ◽  
Author(s):  
Brian J. Duistermars ◽  
Barret D. Pfeiffer ◽  
Eric D. Hoopfer ◽  
David J. Anderson
Keyword(s):  
1995 ◽  
Vol 175 (4) ◽  
pp. 405-421 ◽  
Author(s):  
Eldridge S. Adams ◽  
Michael Mesterton-Gibbons

1983 ◽  
Vol 61 (1) ◽  
pp. 65-69 ◽  
Author(s):  
James A. Darley

The territorial behavior of the female brown-headed cowbird (Molothrus ater) was studied at London, Ontario, in 1966 and 1967. The cowbirds arrived in the study area during the last week of March and the first 2 weeks of April. Adult birds arrived about 2 weeks before the yearlings. Forty-six resident and 56 nonresident females were observed in the study area; these nonresidents appeared to use the area for feeding. The breeding residents established home ranges mainly through the use of threat displays. The defence of these home ranges suggest that they might be classified as territories. Thirty-nine breeding resident females, 17 yearlings, and 22 adults had home ranges ranging from 0.9 to 13.4 ha (average 4.5 ± 0.4 ha).


2009 ◽  
Vol 32 (3-4) ◽  
pp. 249-266 ◽  
Author(s):  
John Archer

AbstractI argue that the magnitude and nature of sex differences in aggression, their development, causation, and variability, can be better explained by sexual selection than by the alternative biosocial version of social role theory. Thus, sex differences in physical aggression increase with the degree of risk, occur early in life, peak in young adulthood, and are likely to be mediated by greater male impulsiveness, and greater female fear of physical danger. Male variability in physical aggression is consistent with an alternative life history perspective, and context-dependent variability with responses to reproductive competition, although some variability follows the internal and external influences of social roles. Other sex differences, in variance in reproductive output, threat displays, size and strength, maturation rates, and mortality and conception rates, all indicate that male aggression is part of a sexually selected adaptive complex. Physical aggression between partners can be explained using different evolutionary principles, arising from the conflicts of interest between males and females entering a reproductive alliance, combined with variability following differences in societal gender roles. In this case, social roles are particularly important since they enable both the relatively equality in physical aggression between partners from Western nations, and the considerable cross-national variability, to be explained.


2003 ◽  
Vol 221 (3) ◽  
pp. 327-348 ◽  
Author(s):  
SZABOLCS SZÁMADÓ
Keyword(s):  

1989 ◽  
Vol 10 (3) ◽  
pp. 331-344 ◽  
Author(s):  
Matthew Kramer ◽  
Enrique Font

AbstractDisplay repertoire analysis requires and unbiased estimate of the number of different displays. Anolis lizards, with easily quantifiable visual displays, provide a system amenable to determining display repertoire size. We used multivariate clustering techniques to classify Anolis equastris headbobbing displays. Forty displays, to conspecifics and mirrors, were graphed and 23 variables from each were used in a cluster analysis. Displays were classified into four distinct groups and a single odd display. The most important variables for classifying displays, assessed with a stepwide discriminant analysis, were associated with the general cadence, number of headbobs, and location of large and small headbobs. Most headbobbing displays ended in lateral head movements, possibly arising from ritualized mouth-wiping. All displays analyzed were apparently aggressive ("threat") displays, suggesting a rich display repertoire for this species but leaving unexplained the reasons so many display types are used. Social and defensive displays, while sharing a number of motor patterns, are readily distinguished by the long duration of dewlap extension and gaping in defensive behavior.


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