Environmental causes for plant biodiversity gradients

被引:44
作者
Davies, TJ
Barraclough, TG
Savolainen, V
Chase, MW
机构
[1] Univ London Imperial Coll Sci & Technol, Dept Biol Sci, Ascot SL5 7PY, Berks, England
[2] Univ London Imperial Coll Sci & Technol, NERC, Ctr Populat Biol, Ascot SL5 7PY, Berks, England
[3] Royal Bot Gardens, Jodrell Lab, Mol Systemat Sect, Richmond TW9 3DS, Surrey, England
关键词
species richness; evolutionary rates; environmental energy; biological traits; angiosperms;
D O I
10.1098/rstb.2004.1524
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
One of the most pervasive patterns observed in biodiversity studies is the tendency for species richness to decline towards the poles. One possible explanation is that high levels of environmental energy promote higher species richness nearer the equator. Energy input may set a limit to the number of species that can coexist in an area or alternatively may influence evolutionary rates. Within flowering plants (angiosperms), families exposed to a high energy load tend to be both more species rich and possess faster evolutionary rates, although there is no evidence that one drives the other. Specific environmental effects are likely to vary among lineages, reflecting the interaction between biological traits and environmental conditions in which they are found. One example of this is demonstrated by the high species richness of the iris family (Iridaceae) in the Cape of South Africa, a likely product of biological traits associated with reproductive isolation and the steep ecological and climatic gradients of the region. Within any set of conditions some lineages will tend to be favoured over others; however, the identity of these lineages will fluctuate with a changing environment, explaining the highly labile nature of diversification rates observed among major lineages of flowering plants.
引用
收藏
页码:1645 / 1656
页数:12
相关论文
共 74 条
[11]   DIOECISM IN TROPICAL FOREST TREES [J].
BAWA, KS ;
OPLER, PA .
EVOLUTION, 1975, 29 (01) :167-179
[12]   Determinants of rate variation in mammalian DNA sequence evolution [J].
Bromham, L ;
Rambaut, A ;
Harvey, PH .
JOURNAL OF MOLECULAR EVOLUTION, 1996, 43 (06) :610-621
[13]   WHY ARE THERE SO MANY KINDS OF FLOWERING PLANTS [J].
BURGER, WC .
BIOSCIENCE, 1981, 31 (08) :572-&
[14]  
CALDWELL M, 1995, AMBIO, V24, P166
[15]   Latitude and rates of diversification in birds and butterflies [J].
Cardillo, M .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1999, 266 (1425) :1221-1225
[16]   PHYLOGENETICS OF SEED PLANTS - AN ANALYSIS OF NUCLEOTIDE-SEQUENCES FROM THE PLASTID GENE RBCL [J].
CHASE, MW ;
SOLTIS, DE ;
OLMSTEAD, RG ;
MORGAN, D ;
LES, DH ;
MISHLER, BD ;
DUVALL, MR ;
PRICE, RA ;
HILLS, HG ;
QIU, YL ;
KRON, KA ;
RETTIG, JH ;
CONTI, E ;
PALMER, JD ;
MANHART, JR ;
SYTSMA, KJ ;
MICHAELS, HJ ;
KRESS, WJ ;
KAROL, KG ;
CLARK, WD ;
HEDREN, M ;
GAUT, BS ;
JANSEN, RK ;
KIM, KJ ;
WIMPEE, CF ;
SMITH, JF ;
FURNIER, GR ;
STRAUSS, SH ;
XIANG, QY ;
PLUNKETT, GM ;
SOLTIS, PS ;
SWENSEN, SM ;
WILLIAMS, SE ;
GADEK, PA ;
QUINN, CJ ;
EGUIARTE, LE ;
GOLENBERG, E ;
LEARN, GH ;
GRAHAM, SW ;
BARRETT, SCH ;
DAYANANDAN, S ;
ALBERT, VA .
ANNALS OF THE MISSOURI BOTANICAL GARDEN, 1993, 80 (03) :528-580
[17]   Plant diversity in Mediterranean-climate regions [J].
Cowling, RM ;
Rundel, PW ;
Lamont, BB ;
Arroyo, MK ;
Arianoutsou, M .
TRENDS IN ECOLOGY & EVOLUTION, 1996, 11 (09) :362-366
[18]  
Cox CB, 2001, J BIOGEOGR, V28, P511
[19]   ANGIOSPERM DIVERSIFICATION AND PALEOLATITUDINAL GRADIENTS IN CRETACEOUS FLORISTIC DIVERSITY [J].
CRANE, PR ;
LIDGARD, S .
SCIENCE, 1989, 246 (4930) :675-678
[20]   THE ORIGIN AND EARLY DIVERSIFICATION OF ANGIOSPERMS [J].
CRANE, PR ;
FRIIS, EM ;
PEDERSEN, KR .
NATURE, 1995, 374 (6517) :27-33