The developmental, physiological, neural, and genetical causes and consequences of frequency-dependent selection in the wild

被引:114
作者
Sinervo, Barry [1 ]
Calsbeek, Ryan
机构
[1] Univ Calif Santa Cruz, Dept Ecol & Evolutionary Biol, Santa Cruz, CA 95064 USA
[2] Dartmouth Coll, Dept Biol Sci, Hanover, NH 03755 USA
关键词
cognition; correlational selection; interspecific interactions; intraspecific; perception; rock-paper-scissors;
D O I
10.1146/annurev.ecolsys.37.091305.110128
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
We outline roles of frequency-dependent selection (FDS) in coadaptation and coevolutionary change. Coadaptation and coevolution occur because correlational selection (CS) and correlated evolution couple many traits. CS arises from causal interactions between traits expressed in two or more interactors, which invariably involve different traits (signalers-receivers). Thus, the causes of CS are due to FDS acting on trait interactions. Negative FDS, a rare advantage, is often coupled to positive FDS generating complex dynamics and FD cycles. Neural mechanisms of learning and perception create analogous routes by which traits are reinforced in cognitive and perceptual systems of interactors, substituting for positive FDS. FDS across all levels of biological organization is thus best understood as proximate causes that link interactors and shape genetic correlations within and among interactors on long timescales, or cognitive trait correlations within interactors on short timescales. We find rock-paper-scissors dynamics are common in nature.
引用
收藏
页码:581 / 610
页数:30
相关论文
共 121 条
[1]   Female sticklebacks Gasterosteus aculeatus use self-reference to optimize MHC allele number during mate selection [J].
Aeschlimann, PB ;
Häberli, MA ;
Reusch, TBH ;
Boehm, T ;
Milinski, M .
BEHAVIORAL ECOLOGY AND SOCIOBIOLOGY, 2003, 54 (02) :119-126
[2]  
Agren J, 1996, EVOLUTION, V50, P126, DOI [10.2307/2410787, 10.1111/j.1558-5646.1996.tb04479.x]
[3]   Rejection of common cuckoo Cuculus canorus eggs in relation to female age in the bluethroat Luscinia svecica [J].
Amundsen, T ;
Brobakken, PT ;
Moksnes, A ;
Roskaft, E .
JOURNAL OF AVIAN BIOLOGY, 2002, 33 (04) :366-370
[4]  
[Anonymous], 1982, EVOLUTION THEORY GAM
[5]   TRILOBITE MALFORMATIONS AND THE FOSSIL RECORD OF BEHAVIORAL ASYMMETRY [J].
BABCOCK, LE .
JOURNAL OF PALEONTOLOGY, 1993, 67 (02) :217-229
[6]  
Barrett SCH, 2004, EVOLUTION, V58, P964, DOI 10.1111/j.0014-3820.2004.tb00431.x
[7]   THE ADVANTAGES AND EVOLUTION OF A MORPHOLOGICAL NOVELTY [J].
BENKMAN, CW ;
LINDHOLM, AK .
NATURE, 1991, 349 (6309) :519-520
[8]   Are the ratios of bill crossing morphs in crossbills the result of frequency-dependent selection? [J].
Benkman, CW .
EVOLUTIONARY ECOLOGY, 1996, 10 (01) :119-126
[9]   MHC studies in nonmodel vertebrates: what have we learned about natural selection in 15 years? [J].
Bernatchez, L ;
Landry, C .
JOURNAL OF EVOLUTIONARY BIOLOGY, 2003, 16 (03) :363-377
[10]   Maintenance of handedness polymorphism in humans: a frequency-dependent selection model [J].
Billiard, S ;
Faurie, C ;
Raymond, M .
JOURNAL OF THEORETICAL BIOLOGY, 2005, 235 (01) :85-93