MBE Advance Access published online on November 10, 2004
Molecular Biology and Evolution, doi:10.1093/molbev/msi042
Molecular Biology and Evolution © Society for Molecular Biology and Evolution 2004; all rights reserved
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Department of Biology, Marine Biology Program, Florida International University, Miami FL 33199 USA
* To whom correspondence should be addressed. Endosymbiotic dinoflagellates, or "zooxanthellae," are required for the survival of a diverse community of invertebrates that construct and dominate shallow, tropical coral reef ecosystems. Molecular systematics applied to this once understudied symbiont partner, Symbiodinium spp., divide the group into divergent lineages or sub-generic "clades." Within each clade, numerous closely related "types," or species, exhibit distinctive host taxon, geographic, and/or environmental distributions. This diversity is greatest in clade C which dominates the Indo-Pacific host fauna, and shares dominance in the Atlantic-Caribbean with clade B. Two "living" ancestors in this group, C1 and C3, are common to both the Indo-Pacific and Atlantic-Caribbean. Each ocean possesses a diverse assemblage that appears to have independently evolved (adaptively radiated) through host specialization and allopatric differentiation. This phylogeographic evidence suggests that a worldwide selective sweep of C1/C3, or their progenitor, must have occurred before both oceans separated. The probable timing of this event corresponds with the major climactic changes and low CO2 levels of the late Miocene and/or early Pliocene. Subsequent bursts of diversification have proceeded in each ocean since this transition. An eco-evolutionary expansion to numerous and taxonomically diverse hosts by a select host-generalist symbiont followed by the onset of rapid diversification suggests a radical process through which coral-algal symbioses respond and persist through the vicissitudes of planetary climate change.
Research Article
"Species" Radiations of Symbiotic Dinoflagellates in the Atlantic and Indo-Pacific since the Miocene-Pliocene Transition
Todd C. LaJeunesse, E-mail: lajeunes{at}fiu.edu
![]()
Abstract ![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
W. Renema, D. R. Bellwood, J. C. Braga, K. Bromfield, R. Hall, K. G. Johnson, P. Lunt, C. P. Meyer, L. B. McMonagle, R. J. Morley, et al. Hopping Hotspots: Global Shifts in Marine Biodiversity Science, August 1, 2008; 321(5889): 654 - 657. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. M. Sampayo, T. Ridgway, P. Bongaerts, and O. Hoegh-Guldberg Bleaching susceptibility and mortality of corals are determined by fine-scale differences in symbiont type PNAS, July 29, 2008; 105(30): 10444 - 10449. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Stat, E. Morris, and R. D. Gates Functional diversity in coral-dinoflagellate symbiosis PNAS, July 8, 2008; 105(27): 9256 - 9261. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Stoeck, S. Jost, and J. Boenigk Multigene phylogenies of clonal Spumella-like strains, a cryptic heterotrophic nanoflagellate, isolated from different geographical regions Int J Syst Evol Microbiol, March 1, 2008; 58(3): 716 - 724. [Abstract] [Full Text] [PDF] |
||||


