Diversity is a fundamental, yet threatened, property of ecological systems. The idea that diversity can itself favour diversification, in an autocatalytic process, is very appealing but remains controversial. Here, we study a generalized model of ecological communities and investigate how the level of initial diversity influences the possibility of evolutionary diversification. We show that even simple models of intra- and inter-specific ecological interactions can predict a positive effect of diversity on diversification: adaptive radiations may require a threshold number of species before kicking-off. We call this phenomenon DDAR (diversity-dependent adaptive radiations) and identify mathematically two distinct pathways connecting diversity to diversification, involving character displacement and the positive diversity-productivity relationship. Our results may explain observed delays in adaptive radiations at the macroscale and diversification patterns reported in experimental microbial communities, and shed new light on the dynamics of ecological diversity, the diversity-dependence of diversification rates, and the consequences of biodiversity loss.
Diversity is a fundamental characteristic of ecological communities, that shows important variation around the globe, impacts many aspects of community and ecosystem functioning, and is globally threatened by human activities1. Deciphering the multifarious relationship between diversity, in particular species number, and ecosystem functioning and stability has constituted one of the most long-lasting research programs in ecology2,3,4.
Given the importance and pervasiveness of diversity, evolutionary ecologists have put a lot of effort into understanding how diversity is generated in communities. For example, it has long been recognized that, when colonizing a habitat with vacant niches, a species may respond to this ‘ecological opportunity’5 by diversifying into several daughter species, each occupying different parts of ecological space. This phenomenon, called an adaptive radiation, is most spectacular in isolated ecosystems such as remote archipelagos, where species colonization is so rare that most, if not all, of species diversity can result from the diversification of an ancestral species5,6. Theoretical models of frequency-dependent ecological interactions have successfully been used to investigate how adaptive radiations could be an outcome of the mutation-selection process7,8,9,10. We now have a good understanding of how phenotypic evolution, by continually reshaping the fitness landscape, can under certain conditions cause species to split into two diverging lineages. This process can repeat itself several times, effectively leading to an adaptive radiation, as it was shown to occur in several models of ecological interactions10.
Among the various consequences of diversity, one particularly popular and controversial hypothesis is that diversity itself promotes diversification, diversity thus driving its own genesis11,12,13. However, whilst the ecological and functional implications of diversity have received considerable attention, its impact on the possibility of evolutionary diversification is still, surprisingly, poorly understood. Evolutionary theory classically investigates whether one species, in an isolated system, evolves to a fitness maximum, at which selection is stabilizing, or to a fitness minimum, at which selection is diversifying. In the former case, the species is said to have attained an evolutionary stable strategy (ESS) and no further change occurs. In the latter case, the species attains an evolutionary unstable strategy and may start to diversify7,14,15,16. However, the evolutionary stability of diverse assemblages is rarely studied in detail16,17. This is unfortunate, considering that most adaptive radiations occur in partly connected systems, combining potentially multiple species colonization events and evolutionary diversification18. It is therefore important to understand how the immigration of one or several species could modify the evolutionary stability of ecological assemblages, and therefore control the occurrence of adaptive radiations19,20.
In this study, we investigate the connection between diversity (initial number of species) and evolutionary stability (the possibility of adaptive diversification) in theoretical ecological communities. We consider a generalized model describing the temporal dynamics of species densities as governed by intra- and inter-specific ecological interactions (Methods section). The model can encompass several classical community ecology models. Species are characterized by their trait value x, and trait values control the intrinsic growth rates (r) and carrying capacities (k) of species, as well as the type and strength of pairwise species interactions (a). Different ecological scenarios correspond to different shapes of functions r, k and a. For numerical applications, we consider three contrasted scenarios representative of standard models of species coexistence, specifically the niche scenario (symmetric competition7,21,22,23); the body-size scenario (asymmetric competition10,24) and the life-history (LH) trade-off scenario (competition-colonization dynamics8,25,26). An overview of the functions corresponding to the three scenarios is provided in Fig. 1 (see Methods section for further details).
For each scenario, we determine the possibility of adaptive radiation by studying the adaptive dynamics of species trait values, as a function of the initial number of species (Methods section). In all three scenarios, we find that the likelihood of adaptive radiation increases with the initial number of species. We show that, over large parts of parameter space, adaptive radiation can occur only if a sufficient initial number of species are present, so that adaptive radiations can be triggered by the arrival of one or more species, a phenomenon we call diversity-dependent adaptive radiation (DDAR). We analyse mathematically the selective causes of this phenomenon and argue that it can explain diversification patterns observed at different spatial and temporal scales. We also discuss the implications of DDAR for the dynamics of diversity, especially in a context of habitat loss.
Diversity-dependent adaptive radiations (DDAR)
We ran simulations of the stochastic mutation-selection process under the three ecological scenarios. We systematically varied the initial number of species between one and five. In simulations started with one species, the species evolved a trait value that, depending on ecological scenario, either maximized carrying capacity (niche), was slightly off maximum carrying capacity (body-size) or conferred very low carrying capacity (LH trade-off; Fig. 2). Following this episode of directional evolution, the species could diversify several times as in a classical adaptive radiation7,9,10. However this did not occur for all ecological scenarios and parameter values. In the niche and body-size scenarios, it occurred only for some parameter combinations and in the LH trade-off scenario it never occurred, regardless of parameters. Instead, the species attained a fitness maximum or evolutionary stable strategy (ESS), precluding diversification (Fig. 2).
In those situations not conducive to adaptive radiation, we observed, in all three scenarios, that evolutionary diversification readily occurred provided sufficient initial diversity (number of species) was present. In other words, adaptive radiation, when impossible starting with one species, often became possible starting from two, three or more species (Fig. 2). Adaptive radiation can thus require some initial diversity, a phenomenon we call (diversity-dependent adaptive radiation) DDAR.
To evaluate the prevalence of DDAR, we used adaptive dynamics methods and numerical continuation, continuously varying two key model parameters in each ecological scenario (Methods section). For diversity levels between one and five, we tracked the location of evolutionary attractors and the changes in their evolutionary stability. Loss of evolutionary stability (bifurcation from ESS to branching point) occurs when one species in the community evolves to a fitness minimum, and thus no longer prevents invasion by nearby trait values (Fig. 2). This represents the disappearance of what is called limiting similarity in the context of the niche scenario, or the niche shadow in the context of LH trade-offs27.
We were thus able to compute the likelihood of diversification (defined as the fraction of parameter space in which diversification can occur), as a function of initial diversity. We found that diversification likelihood increased steadily with diversity, and approached one, in all ecological scenarios: more diverse communities were less likely to be evolutionary stable (Fig. 3a–c). As adaptive radiation requires at least one species in the community to lose evolutionary stability, this pattern might simply reflect the fact that the more species, the greater the chance that one loses evolutionary stability. To account for this effect, we compared our results to the null hypothesis in which the per-species diversification probability stays constant, so that the likelihood of diversification increases geometrically with the number of species: more precisely, if diversification probability is γ for one species, it should be 1−(1−γ)s for s species. As is visible in Fig. 3, the observed increase in diversification likelihood always exceeded this null hypothesis. An extreme example is the LH trade-off scenario, for which diversification likelihood jumped from zero to one between one and three species (Fig. 3). DDAR were thus the only form of radiation in this scenario.
For each parameter combination, we further computed the minimal initial diversity that was necessary to observe adaptive radiations, and identified boundaries in parameter space at which this required diversity level changed. This revealed that parameter space regions conducive to adaptive radiation gradually expand with initial diversity (Fig. 3). The conditions favouring diversification were qualitatively similar to those in the one-species case, but they were less stringent in multi-species communities. For instance, in the niche scenario, diversification is favoured by a smaller width of the competition function, at all diversity levels. But whereas with one species adaptive radiation is possible only if the competition kernel is narrower than the resource function, that is, sa<sk (ref. 7), with two species adaptive radiation is possible even if sa is moderately larger than sk, and with three the constraint on sa is essentially suppressed (Fig. 3). Similarly, in the body-size scenario, diversification is favoured by a narrower competition function and a stronger competitive asymmetry, but conditions become less stringent as diversity increases (Fig. 3). In the LH trade-off scenario, diversification is favoured by a greater trade-off intensity and a lower competitive preemption. Treating initial diversity as a parameter, the prediction common to all three scenarios is that diversification is favoured by greater diversity.
Apart from the minimum level of diversity needed to trigger the initial burst of diversification, DDAR are similar to classical adaptive radiations: diversity builds up in the community, at a pace that gradually slows down until the number of species reaches some plateau (Fig. 4a). The eventual stop of diversification can be explained by classical adaptive radiation theory: as the number of species increases, there is a decline in the diversification rate and an concomittent increase in the rate of extinction (Fig. 4b). Both processes can be attributed to the decrease in the average population density of species, caused by the progressive filling of niche space (Fig. 4c). The main difference between DDAR and classical adaptive radiation is thus the existence of a (potentially long) lagtime before the onset of diversification, corresponding to the time required for immigration processes to bring in sufficient initial diversity (Fig. 4a).
Selective causes of DDAR
Although the numerical computation of fitness landscape curvature suffices to determine changes in evolutionary stability, it does not inform on the selective factors underlying the observed changes. To get general insights into the causal link between diversity and diversification in the initial stages of adaptive radiations, we analysed the curvature of the fitness landscape mathematically, considering a generalized evolutionary attractor in the context of equation (2) (Methods section). We derived the following condition for adaptive radiation to be possible in a community of s species:
Asterisks indicate that quantities are evaluated after coevolution, at an evolutionary singular point. If the condition is verified, at least one species is at a fitness minimum and the species assemblage is not evolutionary stable. Otherwise, the assemblage represents a (local) fitness maximum and diversification is impossible given the current number of species.
Equation (1) generalizes several earlier diversification conditions10. For instance, under the niche scenario with only one species, it reduces to the well-known criterion that the carrying capacity function should be broader than the competition function, that is, sk>sa7. Equation (1) shows that the evolutionary stability of ecological communities can be decomposed into three components:
Hi represents selection to match the habitat. An individual is selected to perform well in its habitat, which in this class of models amounts to maximizing k. This optimization force is frequency- and density-independent.
Ii represents frequency-dependent selection on inter-individual interactions. These include both intra- and inter- specific interactions, weighted by their relative frequencies ( and , respectively). An individual is selected to minimize the average impact other individuals exert on it (hence the minus sign in equation (1)).
B is total community biomass, that is, the summed abundance of all species. It affects all species similarly, by governing the relative importance of Ii. As total biomass increases, Ii contributes proportionally more to selection. This is because the greater total density, the more frequent inter-individual interactions. B expresses the density-dependent nature of selection.
All three components varied with the number of species in our numerical experiments (Supplementary Fig. 1). DDAR indicate that equation (1) was easier to verify as s increased. To dissect the underlying causes, we computed, for each ecological scenario, parameter combination, and diversity level, the value of the three components (Hi, Ii and B) individually. We were thus able to determine the role played by each selection component in the loss of evolutionary stability, for each bifurcation from ESS to diversification (Methods section). We did this separately for each type of evolutionary bifurcation, that is, those occuring between s=1 and s=2 (‘2’ regions in Fig. 3), between s=2 and s=3 (‘3’ regions in Fig. 3, and so on. Results are summarized in Fig. 5a–c.
At low diversity levels the picture was similar in all ecological scenarios: evolutionary bifurcations were caused by variations in Hi, and, to a lesser extent, B, while variations in Ii counteracted the onset of diversification (Fig. 5a–c). This can be understood in terms of two general ecological principles: character displacement and diversity-productivity relationships. Considering first the niche and body-size scenarios, as species diversity increases some species are pushed away from the monospecific attractor, which is close to the resource optimum. As a result of this process, called character displacement5,21, species tend to exploit more peripheral resources (Fig. 2a,b). As such species approach the inflexion point of the resource function, Hi is much less negative, and possibly positive, so that its stabilizing effect weakens or vanishes. Second, a generic property of resource competition models is that total community biomass increases with the number of species, generating a positive diversity-productivity (or diversity-biomass) relationship, a pattern often observed in natural ecosystems1. The reason is that more species collectively exploit a greater range of available resources (niche complementarity). Hence B steadily increases with s (Supplementary Fig. 1). This strengthens the selective impact of Ii (equation (1)), which is disruptive in monospecific communities. Hence, two processes can individually trigger DDAR: (i) character displacement away from the resource optimum, and (ii) the positive diversity-productivity relationship.
The same conclusions hold for the LH trade-off scenario (Fig. 5a–c), though for quite different biological reasons. First, it is not adoption of peripheral resources that causes relaxed stabilizing selection from Hi. Indeed, single species do not evolve to maximize k, but on the contrary adopt low k values (low colonization rates; Fig. 2c). Function k, as it arises from patch dynamics25, has no intermediate maximum or inflexion point, and Hi is always negative (Fig. 1c). In multispecies assemblages, some species adopt higher colonization rates, and thus higher carrying capacity, to compensate for their competitive disadvantage (Fig. 2c). As function k gets flatter as trait value increases (Fig. 1c), the end result is the same as in previous scenarios: Hi becomes less stabilizing for those species pushed away from the monospecific attractor. Second, a positive diversity-productivity relationship is not expected for arbitrary species assemblages in the LH trade-off scenario, owing to the strongly interferential nature of competition and lack of niche complementarity. However, we found such a positive diversity-productivity relationship for coevolved species assemblages (that is, in terms of n*; Supplementary Fig. 1), which are the ones that matter to control diversification (equation (1)).
At higher diversity levels this picture could be significantly altered. In all three scenarios, the variation in Ii reversed, and became favourable to diversification (Fig. 5a–c). In the niche and body-size scenarios, intraspecific interactions are disruptive, as similar individuals exploit similar resources and can escape competition by diverging in trait space. This is the main driving force of classical adaptive radiations7,10. However, with two or more species, this disruptive effect of intraspecific competition is greatly diluted, as a large fraction of interactions (or even most of them, for relatively rare, peripheral species) are heterospecific. The latter are stabilizing, as individuals are selected to avoid engaging in competition with other species. Because of this dilution effect, the value of Ii in equation (1) switched from negative (disruptive) in monospecific communities to positive (stabilizing) in multi-species communities (Supplementary Fig. 1). As diversity increases further, however, species can be so different in trait space that selection on interactions with them, albeit positive, weakens considerably (as we reach the tails of function a; Fig. 1a,b). As a result Ii decreases again, favouring diversification (Fig. 5a–c).
A similar reversal of the effect of Ii occurred in the LH trade-off scenario, while Hi and B otherwise retained their effects. But in the niche and body-size scenarios, further changes occurred. First, the variation in Hi also switched sign (Fig. 5a–b). The interpretation is similar as for Ii: peripheral species are displaced to resource portions, where Hi becomes positive and thus is stabilizing. As diversity increases further, they are pushed far into the tails of function k, and Hi, though still positive, weakens (Fig. 1). The roles of Hi and Ii are thus effectively reversed. Second, component B loses its relative importance (Fig. 5a–b). This echoes the saturating shape of the diversity-productivity relationship: increases in total biomass were most pronounced at low species numbers, and then slowed down (Supplementary Fig. 1).
From these analyses of the selection components, we can thus distinguish two causal pathways connecting diversity to diversification, and explaining the DDAR phenomenon. First, at low diversity levels, the positive effect of diversity on diversification was primarily caused by density- and frequency-independent selection on habitat matching and by the positive diversity-productivity relationship (Fig. 5d). Second, at high-diversity levels, the diversification-promoting effect of diversity was primarily caused by frequency-dependent selection on individual interactions (Fig. 5e). The two pathways operated simultaneously in the LH trade-off scenario at medium diversity levels (Fig. 5c). All three components collaborated to suppress evolutionary stability, making DDAR inevitable (Fig. 3c).
Diversity has long been recognized as a key determinant of the ecological stability of ecosystems1,4, but its implications for evolutionary stability (and evolutionary diversification) are much less understood. The idea that ecological diversity could in itself favour diversification is an intriguing, but difficult to prove, hypothesis. It is usually regarded as requiring complex conditions, involving processes such as niche construction, ecosystem engineering, cross-feeding28 or propagating diversification across trophic levels29. Here, we established a theoretical connection between diversity and evolutionary stability and found that more diverse communities are, all else equal, less likely to be evolutionary stable and more likely to undergo evolutionary diversification, in basic models of ecological interactions. This generates a phenomenon we called diversity-dependent adaptive radiations (DDAR).
Classical adaptive radiation theory predicts that after the initial burst of diversity, diversification should gradually slow down, on the basis that ecological niches get filled and ecological opportunity declines5. This results in a negative relationship between diversity and diversification rate30,31. Such a property is observed in our model, as in many ecological models15,21, where the number of species tends to saturate following an adaptive radiation (Fig. 2). However, in the case of DDAR, the rate of diversification undergoes an initial increase, and effectively follows a hump-shaped curve (Fig. 4b). Our results therefore indicate that the same ecological theory that predicts a negative diversity-diversification relationship can also predict, in the very first stages of adaptive radiations, a positive diversity-diversification relationship. DDAR provides an alternative theoretical explanation to positive diversity-diversification relationships, involving only the shape of natural selection, without resorting to complex ecological scenarios or population genetics arguments11,32.
The mechanisms causing DDAR were largely consistent across ecological scenarios, but depended on the diversity level. We identified two general causal pathways linking diversity to diversification, whose relative importance varied with diversity. Our condition for diversification (equation (1)) generalizes earlier results with important differences: selection on habitat matching is not necessarily stabilizing, selection on inter-individual interactions is not necessarily disruptive, and finally, total biomass plays a key role in determining the relative importance of the two. The latter effect has usually been overlooked in one-species studies, as total biomass is just that of the focal species and is often treated as a constant7,23. In multispecies systems however, total biomass commonly increases with diversity, a pattern known as the positive diversity-productivity relationship1,33,34. We have shown that this relationship between diversity and total biomass contributes to generating a positive impact of diversity on diversification, establishing an interesting connection between the evolutionary stability of communities and a fundamental functional property of ecological systems. Adaptive radiations are classically predicted to occur when there is an ecological opportunity (vacant niches) and strong competition for resources. In our modelling results, ecological opportunity did not increase with diversity, but DDAR can be partly explained by an argument based on competition: greater total abundance (component B) increased the intensity of competition, all else equal, which played some role in triggering diversification, especially at low diversity levels (Fig. 5). However this is only part of the picture, as changes in the distribution of trait values (character displacement) typically had greater importance, and in multi-species communities competition could sometimes hinder, rather than promote, diversification (Fig. 5 and Supplementary Fig. 1).
DDAR can provide a parsimonious explanation to empirical patterns at macro- and micro-scales. At the macroscale, clades sometimes fail to diversify despite apparent ecological opportunity32,35,36,37. Some adaptive radiations present an atypical lagtime before diversity starts to accumulate38,39. For example, Hautmann et al.38 report that rediversification of benthic communities in the late Permian was unusually slow and argue that diversification was delayed for lack of competition and immigration in this system. One of the best documented adaptive radiations, Anolis lizards in the Antilles archipelago, also presents such a puzzling pattern: the first lineages colonizing Puerto Rico did not cause an adaptive radiation, in contrast to other islands36,37. It is only the third37, or perhaps the second36 colonizing lineage that diversified into several species (Fig. 6a). We suggest that could simply be an instance of DDAR, even though other explanations involving environmental or geographical contingencies might be conceived. At the micro-scale, experimental studies of microbial adaptive radiations reported that the addition of a competitor could trigger and hasten evolutionary diversification13,20. This was attributed to an increase in the effective amount of resource competition, which is commonly thought to promote diversification. This is consistent with our finding that an increase in total biomass (component B) can in itself favour diversification, even though this is only one of the different ways through which competitive interactions impact diversification (Fig. 5). A recent study explicitly manipulated initial functional diversity and investigated its consequences on diversification in a microbial system40. As a reanalysis of their data (in terms of species number rather than functional diversity) indicates, a greater initial species richness promoted diversification, at diversity levels similar to those in our models (Fig. 6b). The authors further analysed the resource use profile of new genotypes and found that diversification was associated with a shift to scarcer, peripheral, resources, which is consistent with the first causal pathway we identified (Fig. 5d).
Our findings echo recent developments in evolutionary theory showing that complexity, defined as phenotype dimensionality23,41,42 or overlapping ecological and evolutionary timescales43, can affect the evolutionary stability of a species and promote evolutionary diversification. A general picture is thus emerging: evolutionary diversification is more likely in complex ecological ecosystems, and the conditions permitting adaptive radiation could be much broader than previously thought. More importantly, a positive impact of diversity on diversification would have uniquely important consequences for our understanding of the dynamics of diversity and ecosystem development. It implies the possibility of hysteresis effects in the dynamics of diversity, reminiscent of Allee-effects in population biology44: species loss might not only compromise ecosystem functioning in the short term, but also impair the capacity of ecosystems to restore functions in the long term, once diversity has fallen below some threshold level. Such evolutionary debts40 could prove especially problematic in naturally or anthropogenically isolated ecosystems.
We consider a generalized model describing the ecological dynamics of s species interacting in a community. The model encompasses most particular models of adaptive radiation that have been studied so far, and does not assume particular functional forms, allowing us to derive general insights43,45. The abundance ni of a particular species i changes through time according to
The growth function g(·) should be increasing and satisfy g(1)=0. By far the most common choice is g(·)=1−1/·, corresponding to Lotka–Volterra equations. A generalization is g(·)=(1−1/·β)/β, in which case β=1 yields Lotka–Volterra equations and β=0 Gompertz equations46. For plant communities, an alternative form is g(·)=·−1, following from Wit’s growth model and competitive lotteries47,48. In all cases, the argument of g is the ratio between the intrinsic growth potential of a species (parameter ki at the numerator) over the population density effectively experienced by the species (‘perceived crowding’; denominator). The latter is a weighted summation over all individuals in the community, in which individuals of species j have weight ai,j, capturing the net impact of species j on species i. When numerator and denominator balance out, the species is at an equilibrium abundance. It is common practice to scale parameters so that ai,i=1, which makes ki the carrying capacity of species i, that is, its steady-state abundance when growing alone. Parameter ri governs the timescale of species dynamics, as notably influenced by generation time. Each species is characterized by some functional trait xi (for example, body size), which for simplicity is taken to be scalar. Species traits may affect all parameters of the ecological interactions, and so we let ri=r(xi), ki=k(xi) and ai,j=a(xi, xj), with r, k and a sufficiently smooth functions.
The shapes of functions r,k and a determine the type of ecological interactions at play in the community. Although our generalized model does not put any restriction on the form of interactions, for simulations and numerical investigations we considered three contrasted special cases that have received most attention as adaptive radiation models: (a) the niche scenario, (b) the body-size scenario and (c) the life-history (LH) trade-off scenario (Fig. 1). A full comparison of the three scenarios is provided in Supplementary Table 1. The niche scenario is probably the most classical scenario for adaptive radiations. It is a simple description of how competition for a continuous resource spectrum can result in speciation7,21,22,23. Trait x is a key functional trait describing niche position, such as beak size for granivorous birds feeding on a range of seed sizes. Resources are assumed to be unimodally distributed, and species compete less intensely when they overlap less in the range of resources they utilize, making a an even function of trait difference xi−xj (Fig. 1a). Under the body-size scenario, trait x represents average body-size and larger species are assumed to have a competitive edge over smaller ones10,24. This breaks the symmetry of a with respect to the trait difference and allows it to take values greater than one, which means that inter-specific impact can exceed intraspecific impact (Fig. 1b). Finally, the LH trade-off scenario considers interactions between species that are dominant over different parts of their life cycle9. As an example of this scenario, we consider the classical competition-colonization trade-off: species that are dominant at exploiting local resource patches are less efficient at dispersing and colonizing open portions of the habitat8,25,26. In this case, ni represents the fraction of available spatial localities (sites) occupied by species i in the habitat, and xi is the rate at which it colonizes new patches. The LH trade-off scenario represents an asymmetric form of ecological interactions like the body-size senario, but differs considerably in that function k does not have an intermediate maximum, and function a never shrinks to zero on one side49 (Fig. 1c).
For numerical investigations and simulations, we considered three special cases of the generalized model (2), with a Lotka–Volterra g function and contrasted functional forms for r, k and a, as illustrated in Fig. 1. For the niche and body-size scenarios, the original assumption that k and a are both gaussian can result in undesirable or non robust model behaviours and other functions wih the same qualitative properties are increasingly preferred17,23,50. We thus considered several choices for the functional forms: generalized normal functions (varying exponent from gaussian to quartic), boosted gaussian functions (Gaussian plus a constant), or Lorentzian (Cauchy) functions. As we obtained similar patterns for these different choices, we report results for the functional forms that are simplest and closest to the original modelling choices: (i) in the niche scenario, we used a Lorentzian function for the carrying capacity k and the usual gaussian function for the competition function a; (ii) the body-size scenario, we used a log-normal function for k and the usual gaussian function for a; and (iii) in the LH trade-off scenario, we retained the same assumptions as in the original model26. Full details on the model equations, and the formulation of LH trade-off scenario as an instance of equation (2), are presented in Supplementary Note 1. We note that the methodology could be directly applied to an even broader set of ecological situations, as our model can also generalize other forms of ecological trade-offs (for example, ref. 48) or mutualistic and trophic interactions (for example, the foodweb model by51 can be formulated as a special case of (2)).
We simulated ecological dynamics under the three ecological scenarios, allowing the trait values x of species to evolve through a stochastic clonal mutation-selection process. Equation (2) was integrated using an adaptive fourth-order Runge–Kutta algorithm, incorporating a mutation rate (in the range 10−3 to 10−2), so that at each integration step there was a small chance that a mutation occured. If so, we selected randomly, in proportion to abundance, which genotype was affected, and a small density (10−3) of individuals were then attributed a new trait value, equal to the original trait plus a random deviate taken from a gaussian distribution with mean zero and variance 10−6. To avoid atto-fox effects genotypes which abundance fell below the initial abundance of novel mutants were considered extinct. The composition of the community (trait values, abundances) was recorded every 100 steps for the entire simulation time. The number of species at any time was computed as the number of distinct modes in the distribution of trait values. Extinction and diversification rates were then computed from changes in species number. All simulations were conducted in R52.
Numerical and mathematical analysis
We used adaptive dynamics methods to study the selection gradient on traits xi generated from equation (2), under the assumption of ecological steady state. For each ecological scenario, we continously varied two key model parameters (Supplementary Table 2 for parameter ranges) and tracked the position of evolutionary equilibria (at which all selection gradients vanish) and corresponding species equilibrium abundances, using a numerical continuation approach, for diversity levels between one and five species. We determined the evolutionary stability of evolutionary attractors by numerically computing the curvature of the fitness landscape around every species. Finally, for all evolutionary bifurcations caused by a change in diversity, we computed the associated variation in the three selection components individually. We then calculated their relative importance in causing the observed evolutionary bifurcations, averaged them over all parameter combinations and scaled them so that absolute values add up to 100%. All mathematical calculations and the derivation of equation (1) from equation (2) are provided in Supplementary Note 2, and detailed analyses of evolutionary dynamics in the niche scenario are presented in Supplementary Note 3.
The R code used for evolutionary simulations and analyses is available from the authors upon request. The data that underlie Fig. 6 are available from the authors of the corresponding publications upon request.
How to cite this article: Calcagno, V. et al. Diversity spurs diversification in ecological communities. Nat. Commun. 8, 15810 doi: 10.1038/ncomms15810 (2017).
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Hooper, D. U. et al. Effects of biodiversity on ecosystem functioning: a consensus of current knowledge. Ecol. Monogr. 75, 3–35 (2005).
McCann, K. S. The diversity-stability debate. Nature 405, 228–233 (2000).
Ives, A. R. & Carpenter, S. R. Stability and diversity of ecosystems. Science 317, 58–62 (2007).
Loreau, M. & Mazancourt, C. Biodiversity and ecosystem stability: a synthesis of underlying mechanisms. Ecol. Lett. 16, 106–115 (2013).
Schluter, D. The Ecology of Adaptive Radiation OUP Oxford (2000).
Losos, J. B., Warheit, K. I. & Schoener, T. W. Adaptive differentiation following experimental island colonization in anolis lizards. Nature 387, 70–73 (1997).
Dieckmann, U. & Doebeli, M. On the origin of species by sympatric speciation. Nature 400, 354–357 (1999).
Jansen, V. A. A. & Mulder, G. S. E. E. Evolving biodiversity. Ecol. Lett. 2, 379–386 (1999).
Bonsall, M. B., Jansen, V. A. A. & Hassell, M. P. Life history trade-offs assemble ecological guilds. Science 306, 111–114 (2004).
Doebeli, M. & Dieckmann, U. Evolutionary branching and sympatric speciation caused by different types of ecological interactions. Am. Nat. 156, S77–S101 (2000).
Emerson, B. C. & Kolm, N. Species diversity can drive speciation. Nature 434, 1015–1017 (2005).
Gruner, D. S., Gotelli, N. J., Price, J. P. & Cowie, R. H. Does species richness drive speciation? A reassessment with the Hawaiian biota. Ecography 31, 279–285 (2008).
Bailey, S. F., Dettman, J. R., Rainey, P. B. & Kassen, R. Competition both drives and impedes diversification in a model adaptive radiation. Proc. R. Soc. Lond. B: Biol. Sci. 280, 20131253 (2013).
Abrams, P. A., Matsuda, H. & Harada, Y. Evolutionarily unstable fitness maxima and stable fitness minima of continuous traits. Evolut. Ecol. 7, 465–487 (1993).
Vincent, T. L. & Brown, J. S. Evolutionary Game Theory, Natural Selection, and Darwinian Dynamics Cambridge University Press (2005).
Dercole, F. & Rinaldi, S. Analysis of Evolutionary Processes: the Adaptive Dynamics Approach and its Applications Princeton University Press (2008).
Birand, A. & Barany, E. Evolutionary dynamics through multispecies competition. Theor. Ecol. 7, 367–379 (2014).
Gillespie, R. Community assembly through adaptive radiation in hawaian spiders. Science 303, 356–359 (2004).
Fukami, T., Beaumont, H. J. E., Zhang, X. & Rainey, P. B. Immigration history controls diversification in experimental adaptive radiation. Nature 446, 436–439 (2007).
Zhang, Q.-G., Ellis, R. J. & Godfray, H. C. J. The effect of a competitor on a model adaptive radiation. Evolution 66, 1985–1990 (2012).
Rosenzweig, M. L. Species Diversity in Space and Time Cambridge University Press (1995).
Scheffer, M. & van Nes, E. H. Self-organized similarity, the evolutionary emergence of groups of similar species. Proc. Natl Acad. Sci. USA 103, 6230–6235 (2006).
Doebeli, M. & Ispolatov, I. Complexity and diversity. Science 328, 494–497 (2010).
Taper, M. L. & Case, T. J. Models of character displacement and the theoretical robustness of taxon cycles. Evolution 46, 317–333 (1992).
Tilman, D. Competition and biodiversity in spatially structured habitats. Ecology 75, 2–16 (1994).
Calcagno, V., Mouquet, N., Jarne, P. & David, P. Coexistence in a metacommunity: the competition-colonization trade-off is not dead. Ecol. Lett. 9, 897–907 (2006).
Kinzig, A. P., Levin, S. A., Dushoff, J. & Pacala, S. Limiting similarity, species packing, and system stability for hierarchical competition-colonization models. Am. Nat. 153, 371–383 (1999).
Erwin, D. H. Seeds of diversity. Science 308, 1752–1753 (2005).
Hood, G. R. et al. Sequential divergence and the multiplicative origin of community diversity. Proc. Natl Acad. Sci. USA 112, E5980–E5989 (2015).
Etienne, R. S. & Haegeman, B. A conceptual and statistical framework for adaptive radiations with a key role for diversity dependence. Am. Nat. 180, E75–E89 (2012).
Rabosky, D. L. Diversity-dependence, ecological speciation, and the role of competition in macroevolution. Ann. Rev. Ecol., Evol. Syst. 44, 481–502 (2013).
Yoder, J. et al. Ecological opportunity and the origin of adaptive radiations. J. Evolut. Biol. 23, 1581–1596 (2010).
Loreau, M. & Hector, A. Partitioning selection and complementarity in biodiversity experiments. Nature 412, 72–76 (2001).
Tilman, D. et al. Diversity and productivity in a long-term grassland experiment. Science 294, 843–845 (2001).
Losos, J. Adaptive radiation, ecological opportunity, and evolutionary determinism: american society of naturalists e. o. wilson award address. Am. Nat. 175, 623–639 (2010).
Mahler, D. L., Ingram, T., Revell, L. J. & Losos, J. B. Exceptional convergence on the macroevolutionary landscape in island lizard radiations. Science 341, 292–295 (2013).
Mahler, D. L. et al. Discovery of a giant chameleon-like lizard (Anolis) on hispaniola and its significance to understanding replicated adaptive radiations. Am. Nat. 188, 357–364 (2016).
Hautmann, M. et al. Competition in slow motion: the unusual case of benthic marine communities in the wake of the end-permian mass extinction. Palaeontology 58, 871–901 (2015).
Paun, O. et al. Processes driving the adaptive radiation of a tropical tree (Diospyros, Ebenaceae) in new caledonia, a biodiversity hotspot. Syst. Biol. 65, 212–227 (2016).
Jousset, A., Eisenhauer, N., Merker, M., Mouquet, N. & Scheu, S. High functional diversity stimulates diversification in experimental microbial communities. Sci. Adv. 2, e1600124 (2016).
Débarre, F., Nuismer, S. & Doebeli, M. Multidimensional (co) evolutionary stability. Am. Nat. 184, 158–171 (2014).
Svardal, H., Rueffler, C. & Doebeli, M. Organismal complexity and the potential for evolutionary diversification. Evolution 68, 3248–3259 (2014).
Calcagno, V., Dubosclard, M. & De Mazancourt, C. Rapid exploiter-victim coevolution: the race is not always to the swift. Am. Nat. 176, 198–211 (2010).
Courchamp, F., Clutton-Brock, T. & Grenfell, B. Inverse density dependence and the allee effect. Trends Ecol. Evol. 14, 405–410 (1999).
Gross, T. & Feudel, U. Generalized models as a universal approach to the analysis of nonlinear dynamical systems. Phys. Rev. E 73, 016205 (2006).
Goel, N. S. & Richter-Dyn, N. Stochastic Models in Biology Elsevier (2013).
De Wit, C. & Van den Bergh, J. Competition between herbage plants. J. Agric. Sci. 13, 212–221 (1965).
Muller-Landau, H. C. The tolerance-fecundity trade-off and the maintenance of diversity in seed size. Proc. Natl Acad. Sci. USA 107, 4242–4247 (2010).
Kisdi, E. Evolutionary branching under asymmetric competition. J. Theor. Biol. 197, 149–162 (1999).
Meszéna, G., Gyllenberg, M., Pásztor, L. & Metz, J. A. Competitive exclusion and limiting similarity: a unified theory. Theor. Popul. Biol. 69, 68–87 (2006).
Loeuille, N. & Loreau, M. Evolutionary emergence of size-structured food webs. Proc. Natl Acad. Sci. USA 102, 5761–5766 (2005).
R Development Core Team R. A Language and Environment for Statistical Computing R Foundation for Statistical Computing, Vienna, Austria (2008).
We thank Luke Mahler and Alexandre Jousset for sharing data and Jonathan Losos for input on Anoles. V.C., P.J. and P.D. were funded by grant ANR-BIOADAPT-2012-AFFAIRS. M.L. was supported by the TULIP Laboratory of Excellence (ANR-10-LABX-41) and by the BIOSTASES Advanced Grant, funded by the European Research Council under the European Union’s Horizon 2020 research and innovation programme (grant agreement No 666971).
The authors declare no competing financial interests.
About this article
Cite this article
Calcagno, V., Jarne, P., Loreau, M. et al. Diversity spurs diversification in ecological communities. Nat Commun 8, 15810 (2017). https://doi.org/10.1038/ncomms15810
This article is cited by
Cultivating epizoic diatoms provides insights into the evolution and ecology of both epibionts and hosts
Scientific Reports (2022)
Disentangling the genetic origin of Heracleum persicum (Apiaceae) in Europe: multiple introductions from multiple source populations
Biological Invasions (2021)
Nature Communications (2020)
Journal of Mammary Gland Biology and Neoplasia (2018)