Mutualism with sea anemones triggered the adaptive radiation of clownfishes
© Litsios et al.; licensee BioMed Central Ltd. 2012
Received: 6 June 2012
Accepted: 27 October 2012
Published: 2 November 2012
Adaptive radiation is the process by which a single ancestral species diversifies into many descendants adapted to exploit a wide range of habitats. The appearance of ecological opportunities, or the colonisation or adaptation to novel ecological resources, has been documented to promote adaptive radiation in many classic examples. Mutualistic interactions allow species to access resources untapped by competitors, but evidence shows that the effect of mutualism on species diversification can greatly vary among mutualistic systems. Here, we test whether the development of obligate mutualism with sea anemones allowed the clownfishes to radiate adaptively across the Indian and western Pacific oceans reef habitats.
We show that clownfishes morphological characters are linked with ecological niches associated with the sea anemones. This pattern is consistent with the ecological speciation hypothesis. Furthermore, the clownfishes show an increase in the rate of species diversification as well as rate of morphological evolution compared to their closest relatives without anemone mutualistic associations.
The effect of mutualism on species diversification has only been studied in a limited number of groups. We present a case of adaptive radiation where mutualistic interaction is the likely key innovation, providing new insights into the mechanisms involved in the buildup of biodiversity. Due to a lack of barriers to dispersal, ecological speciation is rare in marine environments. Particular life-history characteristics of clownfishes likely reinforced reproductive isolation between populations, allowing rapid species diversification.
The concept of adaptive radiation has been central to evolutionary biology since Darwin’s work on Galapagos finches [1–3]. The general understanding of this process is that rates of ecomorphological changes and species diversification will be increased by ecological opportunities offering available resources untapped by competing species . Ecological opportunity can arise for four main reasons , the most widely described being the colonisation of geographically isolated areas with depauperate fauna (e.g. cichlid fishes in East-African Great Lakes ). The process is similar in the aftermath of a mass extinction event, which allows surviving species to radiate rapidly by filling the available empty niches . Modification of a resource can also trigger native species radiation as demonstrated by the radiation of Lupinus in high-elevation habitats that appeared during the Andean uplift . Finally, the appearance of a trait allowing new interactions with the environment, or key innovation, can create an opportunity for species radiation . For example, the evolution of antifreeze glycoproteins found in notothenioid fishes of Antarctica is thought to have triggered their adaptive radiation by allowing survival in extreme environments . In an analogous manner to key innovations, the evolution of mutualistic interactions can provide access to previously inaccessible resources. For instance, phytophagous insects host mutualistic microbes, which enable the breakdown and digestion of plant compounds by the insects . While a plethora of case studies showing adaptive radiation driven by ecological opportunity offered by one of the aforementioned possibilities exist , examples involving mutualism are scarce (but see ). Since hosts shifts have allowed ecological speciation in a wide range of organisms, including coral-dwelling fish [13, 14], there is a possibility for ecological speciation to occur in mutualistic systems. However, results from empirical and theoretic studies give contradictory evidence on the effect of mutualism on species diversification [15, 16]. The topic is thus still debated and in need of further case studies.
Interaction matrix between clownfishes and their sea anemone hosts
Examples of ecological speciation events are rare in marine ecosystems. This is likely due to the fact that long-distance dispersal is common among marine organism . However, clownfishes are known to have high larval retention to natal reefs [26, 27]. They are also known to produce species-specific calls [28, 29] that differ among geographic populations . Such properties are likely to have reinforced reproductive isolation by reducing gene-flow between clownfishes populations and thus facilitated ecological speciation processes in clownfishes.
In this study, we test whether the evolution of the mutualism with sea anemone in the clownfishes lineage is a key innovation that led to ecological adaptive radiation (sensu ). We ensure that the clownfishes are monophyletic by building a phylogeny for the Pomacentridae family. Next, we show the occurrence of rapid speciation in the clownfishes by testing whether their diversification rate is higher than that of the other damselfishes. We then use an ordination method on the mutualistic interactions to describe potential ecological niches associated with the sea anemones. We further apply phylogenetic comparative methods to test the association between morphological traits and the putative ecological niches. We finally measure the rate of evolution of the morphological traits to see if they fit the theoretical expectation of faster morphological evolutionary rate [4, 31].
Mutualism and clownfishes phenotype
We collected data on the distribution of clownfishes among the 10 possible sea anemone host species (Table 1; [19, 20, 32]). We applied a multiple correspondence analysis (MCA) on the matrix of mutualistic interactions between sea anemones and clownfishes. The MCA analysis is the counterpart of principal component analysis for categorical data, which shows the underlying structure present in the dataset. We used the axes of the MCA that explained most of the variance in the subsequent analysis. This allowed us to determine in a multivariate space, the characteristics of the ecological niches used by the clownfishes and provided by mutualistic interactions.
We extracted morphological measurements of the damselfish from the literature (mainly from , other sources are listed in the Additional file 1). It is thought that adaptation to sea anemones required modifications of the general shape as well as a change in swimming ability in host specialised clownfish. Indeed, continuous and fast swimming is not needed anymore because specialised species never venture far from their host . We thus collected traits in the literature for all Pomacentridae species present in our phylogeny that are linked with body shape and swimming abilities as well as trophic niche, which is generally linked with habitat in Pomacentridae . This analysis resulted in a matrix of eight morphological traits (maximum standard length, the ratio between standard length and the greatest body depth or “body ratio”, the count of hard and soft dorsal-fin rays, the count of soft anal-fin rays, the count of pectoral-fin rays, the number of gill rakers present on the first gill arch and the number of scales which possess a sensory tube or “lateral-line scales”). Standard length and body ratio describe the overall fish shape, which has been shown to be linked with adaptation towards habitats with differing water velocity regimes [36, 37]. Fin morphology directly influences fish locomotory ability  and gill rakers are used as a proxy for the differentiation along the pelagic-benthic trophic resource axis . The number of lateral-line scales is one of the more pronounced morphological differences between the clownfishes and other damselfishes , and may be of importance in the ecological adaptive radiation. It was not possible to take into account intra-specific variation in our analysis and we recorded a single value per trait estimated as the mean of the values obtained from the literature. To diminish potential allometric effects, all traits were log transformed before further analysis.
Phylogeny and divergence time estimation
We assembled DNA sequence data for 196 Pomacentridae species (170/356 damselfishes, 26/30 clownfishes) spanning all genera in the family (Accession numbers available in Additional file 2). Three cichlid species (Aequidens rivulatus, Thorichthys meeki, Tomocichla sieboldii) were included as outgroups [41, 42]. The concatenated sequence matrix was 6945 bp long and composed of six mitochondrial and three nuclear gene regions (12S, 16S, ATP6-8, COI, cytochrome b, ND3, BMP-4, RAG1 & RAG2). Each DNA region was aligned separately with MUSCLE  and ambiguously aligned nucleotides were removed using Gblocks .
After visually checking the alignment, we used BEAST  to simultaneously infer the phylogeny and estimate divergence times. We used a relaxed clock model, drawing substitution rates from a lognormal distribution. We partitioned the alignment by gene as it outperformed an unpartitioned analysis in Bayes factors in a similar dataset . We selected, using Akaike information criterion values (AIC), the substitution model that fits best each partition with the function “phymltest” available in the Ape package  in R  (see the model choice in Additional file 3). We used the only fossil calibration point available for the basal node of the Pomacentridae to obtain absolute divergence time estimates. The fossil that is the earliest record of Pomacentridae (Monte Bolca, Italy) dates back to 50 million years (MY) , which we used as minimum age with a lognormal prior (mean = 2; sd = 1.2; prior 5-95% = 51.03-103.2) following . We selected a lognormal prior to allow the basal node of the Pomacentridae to reach back to ~105 MY, which is the probable age of the Perciformes [49, 50]. We performed two parallel BEAST runs, each 5*107 generations long and sampled posterior distributions every 1,000 generations. We checked the convergence of the two chains, optimal sampling of model parameters and estimated the burn-in length in Tracer . After the removal of 10,000 trees as burn-in, we merged both runs and inferred a maximum credibility phylogeny using TreeAnnotator . Finally, we resampled from the posterior distribution 100 trees to be used in further analysis. These time calibrated trees are hereafter referred to as the distribution of chronograms. As BEAST also outputs phylograms having branch lengths given in expected number of substitution per site, we applied the same resampling procedure to get a random sample of 100 phylograms. This allowed us to test our hypothesis on two sets of phylogenies instead of possibly biasing our results by choosing arbitrarily a specific branch length unit .
We used the package Diversitree  in R to test whether mutualism with sea anemones is linked with an increased diversification rate in the clownfishes as would be expected under the key innovation hypothesis. We applied the BiSSE method , which evaluates jointly the evolution of a binary character (here presence or absence of mutualism with sea anemones), speciation and extinction rates. As we do not have a complete sampling of the Pomacentridae, we used an extension of the method that deals with incompletely sampled phylogenies . A one-rate birth-death model is fitted to the whole tree and compared, using AIC and Likelihood ratio test, with an alternative model allowing two separate rates of speciation and extinction for clownfishes and damselfishes species. In this particular case, the clownfishes are a monophyletic group nested within the Pomacentridae phylogeny. No known clownfishes species has lost the mutualistic behaviour and we therefore forced the loss of mutualism in the model (parameter q10) to a fixed null value. We optimised the other parameters of the model (rates of speciation, extinction and probability of character change) by Maximum Likelihood estimation independently on each of the 100 randomly sampled chronograms to account for phylogenetic uncertainty. The rate of diversification was calculated by subtracting the extinction rate from the speciation rate.
Phylogenetic signal and phenotype-environment correlation
We estimated the phylogenetic signal in the morphological data on each of the 100 phylograms and chronograms with the K  and λ  indexes as implemented in the Phytools package  in R. Assessing the phylogenetic signal of a trait on both phylograms and chronograms can help choose which branch length unit will be the most appropriate for comparative analysis . For both indexes, a value close to 0 is diagnostic of a weak or nonexistent phylogenetic structure, while values close to one are expected if the data follows a Brownian motion (BM) model of character evolution. We performed randomisation tests for the K and a likelihood ratio test for λ to test for an observed phylogenetic signal significantly greater than 0. We repeated the analysis by taking into account only the clownfishes and this time also measuring the phylogenetic signal of the four first axes of the host usage MCA.
Past competition creating character displacement between related species will result in phenotypes that are correlated with resource usage . We assessed whether the morphological traits collected are linked to host usage in the clownfish by measuring the correlation between each of the first four axes of the MCA and the eight morphological traits. We used phylogenetic generalised least squares (pGLS) as implemented in the caper package in R . The λ parameter, which models the phylogenetic dependency of species trait values  was estimated by Maximum Likelihood and the model was replicated over each tree present in the samples of phylograms and chronograms. We assessed if the morphological variables explained a significant part of the variance in the model by running an ANOVA on the pGLS output.
Morphological evolutionary rate
We measured the differences in rate of morphological evolution between clownfishes and damselfishes by comparing the fit of a single rate BM model to that of a multiple rate model. It has been shown that other models could better fit the data than BM especially in adaptive radiations [58, 59]. We choose to use BM because our goal is solely to compare the relative rate of evolution between groups and not the actual trait values. The single rate model assumes that all lineages accumulate the same amount of morphological variance per unit of time while the multiple model allows clownfishes to have a different rate of evolution than the damselfishes. Both models were specified in the Phytools package  that implements the non-censored version of a typical BROWNIE analysis . The best fitting model was selected according to sample size corrected AIC (AICc). We analysed each of the recorded morphological traits on the two sets of 100 trees randomly sampled from the posterior distributions of phylograms and chronograms.
Phylogenetic inference and divergence time
The estimated age of the root node of the Pomacentridae (~55 MY) was similar to previous findings . We inferred a root age of ~19 MY for the clownfish clade and found the crown Amphiprion group, which holds most of the clownfishes species (25 out of 30 species), to have an age of ~7 MY (Figure 2).We did not include in this divergence time analysis the closure of the Isthmus of Panama. This calibration point, which constrains the split of the pairs Abudefduf concolor/taurus and Abudefduf troschelli/saxatilis was not used, because biogeographic information can be uncertain when constraining the age of species splits [62, 63]. However, we recovered similar dates and confidence intervals as estimated in .
Ecological niche of host usage
Phylogenetic signal in the damselfishes
Dorsal fin soft rays
Dorsal fin hard rays
Anal fin soft rays
Lateral line scales
Pectoral fin rays
Phylogenetic signal of morphology and MCA axes
Dorsal fin hard rays
Dorsal fin soft rays
Anal fin soft rays
Lateral line scales
Pectoral fin rays
Correlation between morphological traits and MCA axes
Dorsal fin hard rays
Dorsal fin soft rays
Anal fin soft ray
Dorsal fin hard rays
Dorsal fin soft rays
Anal fin soft ray
Dorsal fin hard rays
Dorsal fin soft rays
Anal fin soft ray
Dorsal fin hard rays
Dorsal fin soft rays
Anal fin soft ray
Morphological evolutionary rate
Pomacentridae phylogeny and diversification
Our inferred phylogeny was congruent with previous work [17, 41] and showed with high posterior probabilities that clownfish are monophyletic within the Pomacentridae family (Figure 2). We used the BiSSE method  to test if the appearance of mutualism acted as a key innovation and if it is associated with an increase in speciation rate. The BiSSE method is a powerful way to detect shifts in diversification rate linked with a binary trait, but the change of state of the binary trait does not usually correspond to a single monophyletic group as in our case. Nevertheless, we chose the BiSSE method as it takes into account the uncertainty in dating the appearance of mutualism on the phylogeny. Indeed, mutualism with sea anemones likely appeared in the common ancestor of the clownfish, but the stem branch of the group is ~13MY long (Figure 2). It is therefore important, when estimating speciation and extinction rates, to take into account the uncertainty in the time estimates that correspond to the appearance of this behaviour. We also constrained the rate of mutualism loss to be null in the BiSSE model. This takes into account the fact that all clownfish are nowadays mutualistic, but it may slightly bias our analysis as it is not impossible that a clownfish species will eventually revert to a non-mutualistic state. However, we do not think that this parameter will influence significantly our results. Other methods exist to infer speciation rates on phylogenies that do not need prior hypotheses on the location of the shift in rate . In a recent paper , the likely nodes of diversification rate shifts were inferred for four coral reef fish families using relative cladogenesis test  and MEDUSA . The study included the Pomacentridae family and they consistently found across methods that the clownfishes experienced a significant rate increase. The rate shift was either placed at the origin of the clownfish or at the base of the Amphiprion crown group. The fact that a method which does not need a priori information on the location of the diversification rate shift recovered similar result as in our study confirms the strength of the diversification rate shift that occurred in the clownfish clade.
It should be noted that the extinction rate also increases in the clownfishes (Figure 3). A possible explanation is that during the diversification process, some clownfish lineages did not leave any descendants as they were ecologically replaced by other more competitive clownfish species. Such events could have occurred during the long branch that is basal to the Amphiprion crown group. Also, it has been suggested that elevated extinction rates in reef associated fishes could be linked with a potential refuge effect of the coral reefs in the aftermath of prolonged extinction events . Yet, to be able to recover extinction rate with high confidence and test such hypotheses, one would need clownfishes fossils , which are not available. However, when compared to the damselfishes, the diversification rate of the clownfishes was still higher (Figure 3), showing that the extinction rate was not sufficient to slow down diversification .
Effect of mutualism and host-associated niches on clownfishes evolution
We measured the phylogenetic signal of each morphological trait on the samples of chronograms and phylograms for the Pomacentridae (Tables 2 and 3). All traits showed a signal close to one (the expected outcome of BM evolution). However, when assessed only on the clownfish clade, phylogenetic signal dropped and only pectoral rays count had a K significantly larger than 0. Furthermore, the phylogenetic signal of the host usage MCA axes were never significantly different from 0. While interpreting an evolutionary process directly from this result can be problematic , a low phylogenetic signal can be found in lineages that show convergent adaptive evolution , which is likely the case in the clownfishes.
We hypothesised that, following the appearance of mutualism, clownfishes radiated in the niches associated with the sea anemones. We described the most important axes of variation in mutualistic interactions with an MCA. The first axis depicted the generalist-specialist host usage gradient, but all three other axes showed gradients linked with the habitat preferences of the sea anemones. Indeed, clownfishes that interact with sea anemones species living in similar reef micro-habitats (i.e. substrate type, depth) cluster together in the analysis. This suggests that clownfish species are first distributed along a generalist to specialist axis, and then, specialist clownfishes interact only with sea anemone species living in a particular habitat type. This has been shown in a previous empirical study , where clownfish species coexisting in a reef were distributed in different habitats. Ecological sorting of clownfish species along the different ecological gradients linked with their hosts is what is expected if resource competition, which is the main driver of adaptive radiation, acted on the evolutionary process [4, 69].
We tested if the observed resource partitioning in different ecological niches, likely due to past competition between ecologically similar species, resulted in morphological adaptation to resource use (i.e. host and habitat use in clownfishes). We sequentially fitted each MCA axis to a set of morphological traits taking into account the phylogenetic relationships between species. We found that an important part of the variation in the MCA axes could be explained by the morphological traits of our dataset for the first and third axes (Table 4). Increasing number of hosts (represented by increasing values of the MCA 1 axis) was correlated with a bigger size, more hard dorsal and soft anal rays, and more gill rakers, while size was positively correlated with deeper habitats (represented by decreasing values of the MCA 3 axis). In clownfishes, the phenotype-environment correlation relates to both host usage (generalists/specialist gradient) and habitat (substrate, depth). This contrasts with many examples of adaptive radiation, where the resource axis has usually a single dimension representing habitat. Therefore, mutualism can be seen as a a key innovation that offered untapped habitat for colonisation, but also allowed diversification to happen on the host usage resource axes.
The morphological traits studied are primarily used for taxonomic purposes but they can still give important functional information for the evolution of the clownfishes. Size and fin traits are related to the locomotion ability in various types of water velocities, while gill rakers can be used as a proxy for the trophic level. The picture given by our analyses is that generalist clownfishes (e.g. A. clarkii) will likely eat more planktonic food (and thus have more gill rakers) and be better swimmers than specialists, which never leave the close vicinity of their sea anemone host. Clownfishes that interact with sea anemones occurring at deeper depth have also a bigger size, allowing for better locomotion in areas where the water velocity is likely to be higher compared to more shallow and sheltered zones . While our results show correlations between phenotype and environment, we do not test for trait utility. This would require a strict experimental setting that was out of scope for this paper. More studies are definitely needed to better describe the adaptive advantage that those traits may provide in the ecological context of the mutualistic interaction.
Following an ecological opportunity, the rate of morphological evolution is hypothesised to be elevated in the traits that are functionally related to the ecological niches filled during the radiation process [4, 71, 72]. We tested this hypothesis on the eight morphological traits studied and found that, on phylograms, they all evolved at higher rates in clownfishes than in damselfishes (Figure 6). The picture is similar when rates are measured on chronograms, although only four characters are evolving significantly faster in the clownfishes than in the damselfishes in this case. Following the comparison of phylogenetic signal that was made between phylograms and chronograms, phylograms are assumed to give, in this case, more accurate results . The fact that all traits evolve at a higher rate is congruent with the pGLS results, which shows all but two traits (lateral-line scales and body ratio) being significantly linked with host and habitat usage. It is probable that lateral-line scales and body ratio evolutionary rates were accelerated in clownfishes because they are indirectly correlated to the ecological niche through another trait. Thus they would not be themselves correlated to host-usage/habitat but still show accelerated rates of evolution. A clear followup to this broad description of clownfishes morphologies would be to extend our analysis and use a morphometric approach (e.g. ) to be able to give an accurate description of the different clownfishes ecotypes. Further studies will then be needed to test, in an experimental framework, trait utility, which is one of the diagnostic criteria of adaptive radiation . The chemical biology of the interaction between clownfishes and sea anemones is also far from being solved . It is thus possible that unknown characteristics associated for example, with the clownfishes mucus could be linked with the variation in interaction between clownfishes and specific sea anemones.
We did not take into account the distribution of the species in this study. Geographical isolation, coupled with ecological differentiation, could also be at the origin of the evolutionary pattern found here. While several clownfish species are local endemics that likely originated through vicariance events rather than ecological speciation, the majority of the species (17 out of 30) have overlapping distributions centred on the Indo-Malay archipelago. If reproductive isolation was solely due to geography, the latter species would have likely disappeared through hybridisation, which easily happens in captivity . Moreover, clownfishes that have similar MCA values usually do not overlap in geographical distribution (e.g. A. latifasciatus, A. nigripes and A. sandaracinos in Figure 4), and sister species always differ in host usage as can be seen on Figure 7. Such a pattern could indicate that, in a given biogeographic region, only one species per ecological niche can subsist, but also that ecologically similar species evolved independently in geographically separated areas. This outlines the need for a thorough biogeographic analysis that would help clarify the effect of geography on the evolution of the clownfish.
Our study shows that clownfishes likely experienced an adaptive radiation through ecological speciation. The obligate mutualism with sea anemones is thought to be the key innovation that allowed clownfishes to radiate rapidly in untapped ecological niches. As expected under the ecological theory of adaptive radiation , it increased diversification as well as rates of morphological evolution. Clownfishes experienced rapid and convergent morphological changes that were correlated with the different ecological niches offered by the host anemones. In marine environments, barriers to dispersal are uncommon, which makes ecological speciation less likely than in more isolated landscapes . However clownfishes show a very short dispersal period compared to other damselfishes . In conjunction with a high retention of larva to natal reef  and population specific calls , restricted dispersal likely reinforced reproductive isolation between clownfish species allowing for adaptive radiation.
This work was funded by the grant (CRS113-125240) from the Swiss National Science Foundation to N.S., P.B.P. and N.E.Z. C.A.S. received a scholarship from the Summer Undergraduate Research Programme at Lausanne University. We would like to thank A. Dubuis, N. Arrigo, L. Pellissier, A. Kostikova, P-A. Christin, M. Alfaro, N. Alvarez, L. Keller and two anonymous reviewers for their suggestions and comments on previous versions of the manuscript. We thank A. Grutter and K. Cheney for the pictures and Rattlebrained Designs for the clownfish drawing. This work received support from the Vital-IT facilities from the Swiss Institute of Bioinformatics.
- Grant PR: Ecology and evolution of Darwin’s finches. 1986, Princeton (NJ): Princeton University Press, 1-458.Google Scholar
- Givnish TJ: Adaptive radiations and molecular systematics: issues and approaches. Molecular Evolution and Adaptive Radiation. Edited by: Givnish TJ, Systma KJ. 1997, Cambridge, U.K: Cambridge Univ. Press, 1-54.Google Scholar
- Losos JB: Adaptive Radiation, Ecological Opportunity, and Evolutionary Determinism American Society of Naturalists E. O. Wilson Award Address *. Am Nat. 2010, 175: 623-639. 10.1086/652433.PubMedView ArticleGoogle Scholar
- Schluter D: The Ecology of Adaptive Radiation. 2000, Oxford, U.K.: Oxford University PressGoogle Scholar
- Losos JB, Mahler DL: Adaptive Radiation: The Interaction of Ecological Opportunity, Adaptation, and Speciation. Evolution since Darwin: The First 150 Years. Edited by: Bell MA, Futuyma DJ, Eanes WF, Levinton JS. 2010, Sunderland, MA: Sinauer As, 381-420.Google Scholar
- Salzburger W: The interaction of sexually and naturally selected traits in the adaptive radiations of cichlid fishes. Mol Ecol. 2009, 18: 169-185. 10.1111/j.1365-294X.2008.03981.x.PubMedView ArticleGoogle Scholar
- Erwin DH: Lessons from the past: biotic recoveries from mass extinctions. Proc Natl Acad Sci USA. 2001, 98: 5399-5403. 10.1073/pnas.091092698.PubMedPubMed CentralView ArticleGoogle Scholar
- Hughes C, Eastwood R: Island radiation on a continental scale: exceptional rates of plant diversification after uplift of the Andes. Proc Natl Acad Sci USA. 2006, 103: 10334-10339. 10.1073/pnas.0601928103.PubMedPubMed CentralView ArticleGoogle Scholar
- Yoder JB, Clancey E, DES Roches S, Eastman JM, Gentry L, Godsoe W, Hagey TJ, Jochimsen D, Oswald BP, Robertson J, Sarver BJ, Schenk JJ, Spear SF, Harmon LJ: Ecological opportunity and the origin of adaptive radiations. J Evol Biol. 2010, 23: 1581-1596. 10.1111/j.1420-9101.2010.02029.x.PubMedView ArticleGoogle Scholar
- Matschiner M, Hanel R, Salzburger W: On the origin and trigger of the notothenioid adaptive radiation. PLoS One. 2011, 6: e18911-10.1371/journal.pone.0018911.PubMedPubMed CentralView ArticleGoogle Scholar
- Janson EM, Stireman JO, Singer MS, Abbot P: Phytophagous insect-microbe mutualisms and adaptive evolutionary diversification. Evolution. 2008, 62: 997-1012. 10.1111/j.1558-5646.2008.00348.x.PubMedView ArticleGoogle Scholar
- Gómez JM, Verdú M: Mutualism with Plants Drives Primate Diversification. Syst Biol. 2012, 61: 567-577. 10.1093/sysbio/syr127.PubMedView ArticleGoogle Scholar
- Munday PL, van Herwerden L, Dudgeon CL: Evidence for sympatric speciation by host shift in the sea. Curr Biol. 2004, 14: 1498-1504. 10.1016/j.cub.2004.08.029.PubMedView ArticleGoogle Scholar
- Bolnick DI, Fitzpatrick BM: Sympatric speciation: models and empirical evidence. Annu Rev Ecol Evol Syst. 2007, 38: 459-487. 10.1146/annurev.ecolsys.38.091206.095804.View ArticleGoogle Scholar
- Yoder JB, Nuismer SL: When does coevolution promote diversification? Am. Nat. 2010, 176: 802-817. 10.1086/657048.View ArticleGoogle Scholar
- Lengyel S, Gove AD, Latimer AM, Majer JD, Dunn RR: Ants sow the seeds of global diversification in flowering plants. PLoS One. 2009, 4: e5480-10.1371/journal.pone.0005480.PubMedPubMed CentralView ArticleGoogle Scholar
- Quenouille B, Bermingham E, Planes S: Molecular systematics of the damselfishes (Teleostei: Pomacentridae): Bayesian phylogenetic analyses of mitochondrial and nuclear DNA sequences. Mol Phylogenet Evol. 2004, 31: 66-88. 10.1016/S1055-7903(03)00278-1.PubMedView ArticleGoogle Scholar
- Elliott JK, Mariscal RN: Coexistence of nine anemonefish species: differential host and habitat utilization, size and recruitment. Mar Biol. 2001, 138: 23-36. 10.1007/s002270000441.View ArticleGoogle Scholar
- Fautin DG, Allen GR: Anemonefishes and their host sea anemones. 1997, Perth: Western Australian MuseumGoogle Scholar
- Ollerton J, McCollin D, Fautin DG, Allen GR: Finding NEMO: nestedness engendered by mutualistic organization in anemonefish and their hosts. Proc R Soc B. 2007, 274: 591-598. 10.1098/rspb.2006.3758.PubMedPubMed CentralView ArticleGoogle Scholar
- Ricciardi F, Boyer M, Ollerton J: Assemblage and interaction structure of the anemonefish-anemone mutualism across the Manado region of Sulawesi. Indonesia Environ Biol Fishes. 2010, 87: 333-347.View ArticleGoogle Scholar
- Mebs D: Chemical biology of the mutualistic relationships of sea anemones with fish and crustaceans. Toxicon. 2009, 54: 1071-1074. 10.1016/j.toxicon.2009.02.027.PubMedView ArticleGoogle Scholar
- Buston PM, García MB: An extraordinary life span estimate for the clown anemonefish Amphiprion percula. J Fish Biol. 2007, 70: 1710-1719. 10.1111/j.1095-8649.2007.01445.x.View ArticleGoogle Scholar
- Fautin DG: The clownfish sea anemones: Stichodactylidae (Coelenterata: Actinaria) and others sea anemones symbiotic with Pomacentrid fishes. T Am Philos Soc. 1981, 71: 3-115. 10.2307/1006382.View ArticleGoogle Scholar
- Puebla O: Ecological speciation in marine v. freshwater fishes. J Fish Biol. 2009, 75: 960-996. 10.1111/j.1095-8649.2009.02358.x.PubMedView ArticleGoogle Scholar
- Jones GP, Planes S, Thorrold SR: Coral reef fish larvae settle close to home. Curr Biol. 2005, 15: 1314-1318. 10.1016/j.cub.2005.06.061.PubMedView ArticleGoogle Scholar
- Almany GR, Berumen ML, Thorrold SR, Planes S, Jones GP: Local replenishment of coral reef fish populations in a marine reserve. Science. 2007, 316: 742-744. 10.1126/science.1140597.PubMedView ArticleGoogle Scholar
- Parmentier E, Colleye O, Fine ML, Frédérich B, Vandewalle P, Herrel A: Sound production in the clownfish Amphiprion clarkii. Science. 2007, 316: 1006-10.1126/science.1139753.PubMedView ArticleGoogle Scholar
- Colleye O, Vandewalle P, Lanterbecq D, Lecchini D, Parmentier E: Interspecific variation of calls in clownfishes: degree of similarity in closely related species. BMC Evol Biol. 2011, 11: 365-10.1186/1471-2148-11-365.PubMedPubMed CentralView ArticleGoogle Scholar
- Parmentier E, Lagardere JP, Vandewalle P, Fine ML: Geographical Variation in Sound Production in the Anemonefish Amphiprion akallopisos. Proc R Soc B. 2005, 272: 1697-1703. 10.1098/rspb.2005.3146.PubMedPubMed CentralView ArticleGoogle Scholar
- Harmon LJ, Schulte JA, Larson A, Losos JB: Tempo and mode of evolutionary radiation in iguanian lizards. Science. 2003, 301: 961-964. 10.1126/science.1084786.PubMedView ArticleGoogle Scholar
- Allen GR, Drew J, Kaufman L: Amphiprion barberi, a new species of anemonefish (Pomacentridae) from Fiji, Tonga, and Samoa. Aqua. 2008, 14: 105-114.Google Scholar
- Allen GR: Damselfish of the world. 1991, Melle, Germany: Mergus Publishers, 271-Google Scholar
- Elliott JK, Lougheed SC, Bateman B, Mcphee LK, Boag PT: Molecular evolution for the phylogenetic evidence of specialization in anemonefishes. Proc R Soc B. 1999, 266: 677-685. 10.1098/rspb.1999.0689.PubMedPubMed CentralView ArticleGoogle Scholar
- Frédérich B, Fabri G, Lepoint G, Vandewalle P, Parmentier E: Trophic niches of thirteen damselfishes (Pomacentridae) at the Grand Récif of Toliara. Madagascar Ichthyol Res. 2009, 56: 10-17.View ArticleGoogle Scholar
- Clabaut C, Bunje PME, Salzburger W, Meyer A: Geometric morphometric analyses provide evidence for the adaptive character of the Tanganyikan cichlid fish radiations. Evolution. 2007, 61: 560-578. 10.1111/j.1558-5646.2007.00045.x.PubMedView ArticleGoogle Scholar
- Langerhans RB, Layman CA, Langerhans AK, Dewitt TJ: Habitat-associated morphological divergence in two Neotropical fish species. Biol J Linn Soc. 2003, 80: 689-698. 10.1111/j.1095-8312.2003.00266.x.View ArticleGoogle Scholar
- Drucker EG, Lauder GV: Locomotor function of the dorsal fin in teleost fishes: experimental analysis of wake forces in sunfish. J Exp Biol. 2001, 204: 2943-2958.PubMedGoogle Scholar
- Kahilainen KK, Siwertsson A, Gjelland KØ, Knudsen R, Bøhn T, Amundsen P-A: The role of gill raker number variability in adaptive radiation of coregonid fish. Evol Ecol. 2010, 25: 573-588.View ArticleGoogle Scholar
- Allen GR: Damselfishes of the south seas. 1975, Neptune city, N.J: T.F.H. Publications, 240-Google Scholar
- Cowman PF, Bellwood DR: Coral reefs as drivers of cladogenesis: expanding coral reefs, cryptic extinction events, and the development of biodiversity hotspots. J Evol Biol. 2011, 24: 2543-2562. 10.1111/j.1420-9101.2011.02391.x.PubMedView ArticleGoogle Scholar
- Litsios G, Pellissier L, Forest F, Lexer C, Pearman PB, Zimmermann NE, Salamin N: Trophic specialization influences the rate of environmental niche evolution in damselfishes (Pomacentridae). Proc R Soc B. 2012, 279: 3662-3669. 10.1098/rspb.2012.1140.PubMedPubMed CentralView ArticleGoogle Scholar
- Edgar RC: MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004, 32: 1792-1797. 10.1093/nar/gkh340.PubMedPubMed CentralView ArticleGoogle Scholar
- Talavera G, Castresana J: Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments. Syst Biol. 2007, 56: 564-577. 10.1080/10635150701472164.PubMedView ArticleGoogle Scholar
- Drummond AJ, Rambaut A: BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol Biol. 2007, 7: 214-10.1186/1471-2148-7-214.PubMedPubMed CentralView ArticleGoogle Scholar
- Paradis E, Claude J, Strimmer K: APE: Analyses of Phylogenetics and Evolution in R language. Bioinformatics. 2004, 20: 289-290. 10.1093/bioinformatics/btg412.PubMedView ArticleGoogle Scholar
- R Development Core Team: R: A Language and Environment for Statistical Computing. 2011, Vienna, Austria: R Foundation for Statistical ComputingGoogle Scholar
- Bellwood DR, Sorbini L: A review of the fossil record of the Pomacentridae (Teleostei: Labroidei) with a description of a new genus and species from the Eocene of Monte Bolca. Italy Zool J Linn Soc. 1996, 117: 159-174. 10.1111/j.1096-3642.1996.tb02154.x.View ArticleGoogle Scholar
- Santini F, Harmon LJ, Carnevale G, Alfaro ME: Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes. BMC Evol Biol. 2009, 9: 194-10.1186/1471-2148-9-194.PubMedPubMed CentralView ArticleGoogle Scholar
- Near TJ, Eytan RI, Dornburg A, Kuhn KL, Moore Ja, Davis MP, Wainwright PC, Friedman M, Smith WL: Resolution of ray-finned fish phylogeny and timing of diversification. Proc Natl Acad Sci USA. 2012, 109: 13698-13703. 10.1073/pnas.1206625109.PubMedPubMed CentralView ArticleGoogle Scholar
- Litsios G, Salamin N: Effects of Phylogenetic Signal on Ancestral State Reconstruction. Syst Biol. 2012, 61: 533-538. 10.1093/sysbio/syr124.PubMedView ArticleGoogle Scholar
- FitzJohn RG, Maddison WP, Otto SP: Estimating trait-dependent speciation and extinction rates from incompletely resolved phylogenies. Syst Biol. 2009, 58: 595-611. 10.1093/sysbio/syp067.PubMedView ArticleGoogle Scholar
- Maddison WP, Midford PE, Otto SP: Estimating a binary character’s effect on speciation and extinction. Syst Biol. 2007, 56: 701-710. 10.1080/10635150701607033.PubMedView ArticleGoogle Scholar
- Blomberg SP, Garland T, Ives AR: Testing for phylogenetic signal in comparative data: behavioral traits are more labile. Evolution. 2003, 57: 717-745.PubMedView ArticleGoogle Scholar
- Pagel M: Inferring the historical patterns of biological evolution. Nature. 1999, 401: 877-884. 10.1038/44766.PubMedView ArticleGoogle Scholar
- Revell LJ: phytools: an R package for phylogenetic comparative biology (and other things). Methods Ecol Evol. 2012, 3: 217-223. 10.1111/j.2041-210X.2011.00169.x.View ArticleGoogle Scholar
- Orme CDL, Freckleton RP, Thomas GH, Petzoldt T, Fritz S: caper: Comparative Analyses of Phylogenetics and Evolution in R. 2011, [http://R-Forge.R-project.org/projects/caper/]Google Scholar
- Freckleton RP, Harvey PH: Detecting non-Brownian trait evolution in adaptive radiations. PLoS Biol. 2006, 4: e373-10.1371/journal.pbio.0040373.PubMedPubMed CentralView ArticleGoogle Scholar
- Agrawal AA, Fishbein M, Halitschke R, Hastings AP, Rabosky DL, Rasmann S: Evidence for adaptive radiation from a phylogenetic study of plant defenses. Proc Natl Acad Sci USA. 2009, 106: 18067-18072. 10.1073/pnas.0904862106.PubMedPubMed CentralView ArticleGoogle Scholar
- O’Meara BC, Ané C, Sanderson MJ, Wainwright PC: Testing for different rates of continuous trait evolution using likelihood. Evolution. 2006, 60: 922-933.PubMedView ArticleGoogle Scholar
- Cooper JW, Smith LL, Westneat MW: Exploring the radiation of a diverse reef fish family: phylogenetics of the damselfishes (Pomacentridae), with new classifications based on molecular analyses of all genera. Mol Phylogenet Evol. 2009, 52: 1-16. 10.1016/j.ympev.2008.12.010.View ArticleGoogle Scholar
- Marko PB: Fossil calibration of molecular clocks and the divergence times of geminate species pairs separated by the isthmus of panama. Mol Biol Evol. 2002, 19: 2005-2021. 10.1093/oxfordjournals.molbev.a004024.PubMedView ArticleGoogle Scholar
- Lessios HA: The Great American Schism: Divergence of Marine Organisms After the Rise of the Central American Isthmus. Annu Rev Ecol Evol Syst. 2008, 39: 63-91. 10.1146/annurev.ecolsys.38.091206.095815.View ArticleGoogle Scholar
- Alfaro ME, Santini F, Brock C, Alamillo H, Dornburg A, Rabosky DL, Carnevale G, Harmon LJ: Nine exceptional radiations plus high turnover explain species diversity in jawed vertebrates. Proc Natl Acad Sci USA. 2009, 106: 13410-13414. 10.1073/pnas.0811087106.PubMedPubMed CentralView ArticleGoogle Scholar
- Nee S: Mooers a O, Harvey PH: Tempo and mode of evolution revealed from molecular phylogenies. Proc Natl Acad Sci USA. 1992, 89: 8322-8326. 10.1073/pnas.89.17.8322.PubMedPubMed CentralView ArticleGoogle Scholar
- Rabosky DL: Extinction rates should not be estimated from molecular phylogenies. Evolution. 2010, 64: 1816-2184. 10.1111/j.1558-5646.2009.00926.x.PubMedView ArticleGoogle Scholar
- Revell LJ, Harmon LJ, Collar DC: Phylogenetic signal, evolutionary process, and rate. Syst Biol. 2008, 57: 591-601. 10.1080/10635150802302427.PubMedView ArticleGoogle Scholar
- Ackerly D: Conservatism and diversification of plant functional traits: Evolutionary rates versus phylogenetic signal. Proc Natl Acad Sci USA. 2009, 106 (Suppl): 19699-19706. 10.1073/pnas.0901635106.PubMedPubMed CentralView ArticleGoogle Scholar
- Losos JB: Lizards in an evolutionary tree: ecology and adaptive radiation of anoles. 2009, Berkeley: University of California Press, 528-Google Scholar
- Bellwood DR, Wainwright PC: Locomotion in labrid fishes: implications for habitat use and cross-shelf biogeography on the Great Barrier Reef. Coral Reefs. 2001, 20: 139-150. 10.1007/s003380100156.View ArticleGoogle Scholar
- Lovette IJ, Bermingham E, Ricklefs RE: Clade-specific morphological diversification and adaptive radiation in Hawaiian songbirds. Proc R Soc B. 2002, 269: 37-42. 10.1098/rspb.2001.1789.PubMedPubMed CentralView ArticleGoogle Scholar
- Harmon LJ, Melville J, Larson A, Losos JB: The role of geography and ecological opportunity in the diversification of day geckos (Phelsuma). Syst Biol. 2008, 57: 562-573. 10.1080/10635150802304779.PubMedView ArticleGoogle Scholar
- Pushparaj A: Intra specific hybridization between Amhiprion sebae and A. polymnus under captive conditions. Int J Biological Technology. 2010, 1: 52-56.Google Scholar
- Thresher RE, Colin PL, Bell LJ: Planktonic Duration, Distribution and Population Structure of Western and Central Pacific Damselfishes (Pomacentridae). Copeia. 1989, 1989: 420-434. 10.2307/1445439.View ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.