The evolution of body size: What keeps organisms small?

被引:977
作者
Blanckenhorn, WU [1 ]
机构
[1] Univ Zurich, Zool Museum, CH-8057 Zurich, Switzerland
关键词
D O I
10.1086/393620
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is widely agreed that fecundity selection and sexual selection are the major evolutionary forces that select for larger body size in moss organisms. The general, equilibrium view is that selection for large body size is eventually counterbalanced by opposing selective forces. While the evidence for selection favoring larger body size is overwhelming, counterbalancing selection favoring small body size is often masked by the good condition of the larger organism and is therefore less obvious. The suggested costs of large size are: (1) viability costs in juveniles due to long development and/or fast growth; (2) viability costs in adults and juveniles due to predation, parasitism, or starvation because of reduced agility, increased detectability, higher energy requirements, heat stress, and/or intrinsic costs of reproduction; (3) decreased mating success of large males due to reduced agility and/or high energy requiremats;and (4) decreased reproductive success of large females and males due to late reproduction. A review of the literature indicates a substantial lack of empirical evidence for these various mechanisms and highlights the need for experimental studies that specifically address the fitness costs of being large at the ecological, physiological, and genetic levels. Specifically, theoretical investigations and comprehensive case studies of particular model species are needed to elucidate whether sporadic selection in time and space is sufficient to counter balance perpetual and strong selection for large body size.
引用
收藏
页码:385 / 407
页数:23
相关论文
共 247 条
[1]   The effect of flexible growth rates on optimal sizes and development times in a seasonal environment [J].
Abrams, PA ;
Leimar, O ;
Nylin, S ;
Wiklund, C .
AMERICAN NATURALIST, 1996, 147 (03) :381-395
[2]   LOADING CONSTRAINTS SEXUAL SELECTION AND ASSORTATIVE MATING IN PERACARID CRUSTACEA [J].
ADAMS, J ;
GREENWOOD, PJ .
JOURNAL OF ZOOLOGY, 1987, 211 :35-46
[3]   PHENOTYPIC SELECTION ON HERITABLE SIZE TRAITS - ENVIRONMENTAL VARIANCE AND GENETIC RESPONSE [J].
ALATALO, RV ;
GUSTAFSSON, L ;
LUNDBERG, A .
AMERICAN NATURALIST, 1990, 135 (03) :464-471
[4]  
ALATALO RV, 1986, EVOLUTION, V40, P574, DOI 10.1111/j.1558-5646.1986.tb00508.x
[5]   PERSISTENT SIZE VARIATION IN THE ANTHOPHORINE BEE CENTRIS-PALLIDA (APIDAE) DESPITE A LARGE MALE MATING ADVANTAGE [J].
ALCOCK, J .
ECOLOGICAL ENTOMOLOGY, 1995, 20 (01) :1-4
[6]   Male size and survival: The effects of male combat and bird predation in Dawson's burrowing bees, Amegilla dawsoni [J].
Alcock, J .
ECOLOGICAL ENTOMOLOGY, 1996, 21 (04) :309-316
[7]   Competition from large males and the alternative mating tactics of small males of Dawson's burrowing bee (Amegilla dawsoni) (Apidae, Apinae, Anthophorini) [J].
Alcock, J .
JOURNAL OF INSECT BEHAVIOR, 1997, 10 (01) :99-113
[8]  
Alcock J, 1997, J ZOOL, V242, P453
[9]   EVOLUTION OF REVERSED SEXUAL SIZE DIMORPHISM AND ROLE PARTITIONING AMONG PREDATORY BIRDS, WITH A SIZE SCALING OF FLIGHT PERFORMANCE [J].
ANDERSSON, M ;
NORBERG, RA .
BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, 1981, 15 (02) :105-130
[10]   MEASURING SELECTION ON A POPULATION OF DAMSELFLIES WITH A MANIPULATED PHENOTYPE [J].
ANHOLT, BR .
EVOLUTION, 1991, 45 (05) :1091-1106