Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
PLoS One
2018 Jan 01;133:e0194575. doi: 10.1371/journal.pone.0194575.
Show Gene links
Show Anatomy links
Diversification rates indicate an early role of adaptive radiations at the origin of modern echinoid fauna.
Boivin S
,
Saucède T
,
Laffont R
,
Steimetz E
,
Neige P
.
Abstract
Evolutionary radiations are fascinating phenomena corresponding to a dramatic diversification of taxa and a burst of cladogenesis over short periods of time. Most evolutionary radiations have long been regarded as adaptive but this has seldom been demonstrated with large-scale comparative datasets including fossil data. Originating in the Early Jurassic, irregular echinoids are emblematic of the spectacular diversification of mobile marine faunas during the Mesozoic Marine Revolution. They diversified as they colonized various habitats, and now constitute the main component of echinoid fauna in modern seas. The evolutionary radiation of irregular echinoids has long been considered as adaptive but this hypothesis has never been tested. In the present work we analyze the evolution of echinoid species richness and morphological disparity over 37 million years based on an extensive fossil dataset. Our results demonstrate that morphological and functional diversifications in certain clades of irregular echinoids were exceptionally high compared to other clades and that they were associated with the evolution of new modes of life and so can be defined as adaptive radiations. The role played by ecological opportunities in the diversification of these clades was critical, with the evolution of the infaunal mode of life promoting the adaptive radiation of irregular echinoids.
Fig 1. Phylogeny of main Jurassic echinoid clades.Phylogenetic relationships between clades and estimated times of divergence (in millions of years) are based on Kroh and Smith [73]. Clades are a mix of higher taxonomic ranks. Crosses indicate extinct clades. The green area corresponds to the studied time interval. Ages in millions of years Before Present (after Gradstein et al. [74]).
Fig 2. Landmark position.Landmarks (red dots) are positioned at the junction between the perradial suture lines (central line of each ambulacrum) and the peristome edge (five inner landmarks) and between the perradial suture lines and the ambitus (five outer landmarks). Roman numerals refer to the echinoid’s five ambulacra.
Fig 3. Taxonomic diversity and disparity of Jurassic echinoids.Individual contribution of echinoid clades to total taxonomic diversity and disparity levels for the studied time period. Colored areas show the values for irregular echinoid clades. Areas in white and grey are for regular echinoid clades. Poly: Polycidaridae, Cid: Cidaridae, Aulo: Aulodonts, Hemi: Hemicidaridae, Ps: Pseudodiadematidae, Cal: Calycina, Ech: Echinacea, Orth: Orthopsidae, Eo: Eognathostomata, Deso: Desorellidae, Neo: Neognathostomata, Atelo: Atelostomata.
Fig 4. Morphospace plot of echinoid disparity.Black symbols correspond to the specimens of regular echinoids, yellow, blue, green, and red symbols represent irregular echinoids. Outlines shown for representative specimens among Cidaridae, Eognathostomata, Desorellidae, Neognathostomata, and Atelostomata. Poly: Polycidaridae, Cid: Cidaridae, Aulo: Aulodonts, Hemi: Hemicidaridae, Ps: Pseudodiadematidae, Cal: Calycina, Ech: Echinacea, Orth: Orthopsidae, Eo: Eognathostomata, Deso: Desorellidae, Neo: Neognathostomata, Atelo: Atelostomata.
Fig 5. Richness and disparity levels of main Jurassic echinoid clades in relation with their feeding strategies and modes of life.The spindle diagram shows taxonomic diversity and disparity levels for the 12 Jurassic echinoid clades. For each clade, taxonomic diversity is expressed as species richness for each geological stage, the wider the rectangles, the higher the number of species. Colors correspond to the tested disparity values relative to other clades: unusually high (red), normal (orange), unusually low (yellow), not tested due to lack of data (white). Main feeding strategies and modes of life were interpreted for each clade. Ages in million of years Before Present (after Gradstein et al. [73]).
Fig 6. Biplot of species richness and disparity.Species richness (expressed in number of species) is plotted against disparity (expressed as the Mean Pairwise Distance) for each clade and each time interval. The four clades of irregular echinoids are plotted separately from the others (respectively A and B).
Adams,
Are rates of species diversification correlated with rates of morphological evolution?
2009, Pubmed
Adams,
Are rates of species diversification correlated with rates of morphological evolution?
2009,
Pubmed
Aguilée,
Adaptive radiation driven by the interplay of eco-evolutionary and landscape dynamics.
2013,
Pubmed
Benson,
Rates of dinosaur body mass evolution indicate 170 million years of sustained ecological innovation on the avian stem lineage.
2014,
Pubmed
Bookstein,
Landmark methods for forms without landmarks: morphometrics of group differences in outline shape.
1997,
Pubmed
Brayard,
Good genes and good luck: ammonoid diversity and the end-Permian mass extinction.
2009,
Pubmed
Erwin,
Lessons from the past: biotic recoveries from mass extinctions.
2001,
Pubmed
Gavrilets,
Models of speciation: where are we now?
2014,
Pubmed
Gavrilets,
Adaptive radiation: contrasting theory with data.
2009,
Pubmed
Harmon,
Early bursts of body size and shape evolution are rare in comparative data.
2010,
Pubmed
Harmon,
Tempo and mode of evolutionary radiation in iguanian lizards.
2003,
Pubmed
Hopkins,
Dynamic evolutionary change in post-Paleozoic echinoids and the importance of scale when interpreting changes in rates of evolution.
2015,
Pubmed
Hughes,
Clades reach highest morphological disparity early in their evolution.
2013,
Pubmed
Jackson,
What can we learn about ecology and evolution from the fossil record?
2006,
Pubmed
Kozak,
Rapid lineage accumulation in a non-adaptive radiation: phylogenetic analysis of diversification rates in eastern North American woodland salamanders (Plethodontidae: Plethodon).
2006,
Pubmed
Lecointre,
Is the species flock concept operational? The Antarctic shelf case.
2013,
Pubmed
,
Echinobase
Losos,
Adaptive radiation, ecological opportunity, and evolutionary determinism. American Society of Naturalists E. O. Wilson award address.
2010,
Pubmed
Losos,
Testing the hypothesis that a clade has adaptively radiated: iguanid lizard clades as a case study.
2002,
Pubmed
Moen,
From dinosaurs to modern bird diversity: extending the time scale of adaptive radiation.
2014,
Pubmed
Morlon,
Phylogenetic approaches for studying diversification.
2014,
Pubmed
Rabosky,
Rates of morphological evolution are correlated with species richness in salamanders.
2012,
Pubmed
Ricklefs,
Time, species, and the generation of trait variance in clades.
2006,
Pubmed
Roy,
Morphological approaches to measuring biodiversity.
1997,
Pubmed
Sepkoski,
Limits to randomness in paleobiologic models: the case of Phanerozoic species diversity.
1994,
Pubmed
Simões,
The Evolving Theory of Evolutionary Radiations.
2016,
Pubmed
Smith,
Testing the molecular clock: molecular and paleontological estimates of divergence times in the Echinoidea (Echinodermata).
2006,
Pubmed
,
Echinobase
Yoder,
Ecological opportunity and the origin of adaptive radiations.
2010,
Pubmed