Global patterns of diversification and species richness in amphibians

被引:216
作者
Wiens, John J. [1 ]
机构
[1] SUNY Stony Brook, Dept Ecol & Evolut, Stony Brook, NY 11794 USA
关键词
amphibians; biogeography; diversification; phylogeny; speciation; species richness;
D O I
10.1086/519396
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Geographic patterns of species richness ultimately arise through the processes of speciation, extinction, and dispersal, but relatively few studies consider evolutionary and biogeographic processes in explaining these diversity patterns. One explanation for high tropical species richness is that many species- rich clades originated in tropical regions and spread to temperate regions infrequently and more recently, leaving little time for species richness to accumulate there ( assuming similar rates of diversification in temperate and tropical regions). However, the major clades of anurans ( frogs) and salamanders may offer a compelling counterexample. Most salamander families are predominately temperate in distribution, but the one primarily tropical clade ( Bolitoglossinae) contains nearly half of all salamander species. Similarly, most basal clades of anurans are predominately temperate, but one largely tropical clade ( Neobatrachia) contains similar to 96% of anurans. In this article, I examine patterns of diversification in frogs and salamanders and their relationship to large- scale patterns of species richness in amphibians. I find that diversification rates in both frogs and salamanders increase significantly with decreasing latitude. These results may shed light on both the evolutionary causes of the latitudinal diversity gradient and the dramatic but poorly explained disparities in the diversity of living amphibian clades.
引用
收藏
页码:S86 / S106
页数:21
相关论文
共 96 条
[71]   NEUROANATOMY INFLUENCES SPECIATION RATES AMONG ANURANS [J].
RYAN, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (05) :1379-1382
[72]   Initial diversification of living amphibians predated the breakup of Pangaea [J].
San Mauro, D ;
Vences, M ;
Alcobendas, M ;
Zardoya, R ;
Meyer, A .
AMERICAN NATURALIST, 2005, 165 (05) :590-599
[73]  
Sanchiz B., 1979, ANN NATURHISTORISC A, V24, P153
[74]   Estimating absolute rates of molecular evolution and divergence times: A penalized likelihood approach [J].
Sanderson, MJ .
MOLECULAR BIOLOGY AND EVOLUTION, 2002, 19 (01) :101-109
[75]   r8s: inferring absolute rates of molecular evolution and divergence times in the absence of a molecular clock [J].
Sanderson, MJ .
BIOINFORMATICS, 2003, 19 (02) :301-302
[76]   Southern Hemisphere biogeography inferred by event-based models:: Plant versus animal patterns [J].
Sanmartín, I ;
Ronquist, F .
SYSTEMATIC BIOLOGY, 2004, 53 (02) :216-243
[77]   WHEN MOLECULES AND MORPHOLOGY CLASH - A PHYLOGENETIC ANALYSIS OF THE NORTH-AMERICAN AMBYSTOMATID SALAMANDERS (CAUDATA, AMBYSTOMATIDAE) [J].
SHAFFER, HB ;
CLARK, JM ;
KRAUS, F .
SYSTEMATIC ZOOLOGY, 1991, 40 (03) :284-303
[78]  
Smith SA, 2005, EVOLUTION, V59, P2433
[79]  
Stebbins GL, 1974, FLOWERING PLANTS EVO
[80]   Testing hypotheses of speciation timing in Dicamptodon copei and Dicamptodon aterrimus (Caudata: Dicamptodontidae) [J].
Steele, CA ;
Carstens, BC ;
Storfer, A ;
Sullivan, J .
MOLECULAR PHYLOGENETICS AND EVOLUTION, 2005, 36 (01) :90-100