Resource Competition and Coevolution in Sticklebacks
© Springer Science+Business Media, LLC 2010
Published: 15 January 2010
Threespine stickleback in young postglacial lakes provide a compelling example of coevolution between species that compete for resources. Coexisting pairs of stickleback species are highly divergent in habitat, diet, and body size and shape, whereas stickleback occurring alone in lakes are intermediate. We used experiments in ponds to test mechanisms of divergence between coexisting species. The results support the hypothesis of coevolution by resource competition between stickleback, but we found evidence that interactions with natural enemies also contribute to divergence. Natural selection arising from these interactions selects against intermediate phenotypes, included hybrids, and thus has contributed to the origin and persistence of stickleback species.
I address the consequences of coevolution resulting from interspecific competition for resources—also known as “character displacement” (Brown and Wilson 1956) and “coevolutionary displacement” (Thompson 2005). By resource competition I mean the negative impact of one species on another resulting from consumption and depletion of shared resources. Competition occurs frequently between species in nature, but it is not as obvious as some of the other interactions discussed in this issue. Resource competitors do not usually kill, eat, nourish, help, or live on or inside one another. Individuals of two species sharing a resource need not even meet to compete. Competition results indirectly from the changes each interacting species makes to its food supply in the environment. The interaction is thus not observed directly, but must be inferred from experiments or by careful measurements of food depletion and its impacts.
Competition has long been thought to be one of the most important interactions in nature, with widespread evolutionary consequences. Many of the naturalists studying evolution in the last century believed that this interaction was one of the main drivers of differentiation between closely related species. Darwin (1859) thought that competition was important in the very origin of new species. Without resource competition, it was believed, the breadth of life's diversity on earth would be much less than it actually is.
The trouble with patterns like those in Fig. 1, however, is that they don’t get at the underlying mechanism. Competition and coevolution provides a plausible explanation for trait differences between coexisting species, but unfortunately it is not the only explanation. Since Lack (1947) and Brown and Wilson (1956), many alternative explanations for such patterns have been suggested. For example, the pattern might be due to chance, or it might reflect systematic differences between environments where species occur together and where they occur separately. The shifts might be non-genetic and reflect phenotypically plastic changes instead. Or, the mechanism driving divergence might be some other interaction besides resource competition, such as predation or reproductive interference. In a few instances, further study found that one or more alternatives to competition provided a superior explanation (Grant 1975; Gorbushin 1996).
For these reasons, evaluating the role of competition and coevolution in the evolution of diversity must go beyond pattern to illuminate the mechanisms driving divergence. Intensive recent research on a few systems, including Darwin's finches (Grant and Grant 2006), spadefoot toads (Pfennig and Murphy 2000), Caribbean island lizards (Losos 2009) and threespine stickleback (Schluter and McPhail 1992; Schluter 2003) have helped to build a more comprehensive picture of the role of competition and coevolution. In this article, I give an overview of progress from studies of one of these groups, the threespine stickleback of small coastal lakes in British Columbia, Canada. These fish show clear patterns like that presented by Lack (1947) on the Galápagos finches, but the stickleback have the additional advantage that it is possible to carry out manipulative experiments.
Our initial aim in the stickleback project was to use experiments to conduct strong tests of the hypothesis of competition and coevolution between coexisting species (“we” and “us” includes myself, students, and collaborators). Along the way we made some unexpected discoveries that indicated both that the effects of competition and coevolution were more far-reaching than we first thought, and at the same time that competition was not the whole story. I highlight some of the still-open questions that these new findings raised, and that will continue to drive research into this system in future.
Patterns of Trait Shift in Threespine Stickleback
Remarkably, the genetic and geological data indicate that the limnetic and benthic species in different lakes have multiple origins (Taylor and McPhail 1999, 2000). The limnetic species in one lake is not the closest relative to the limnetics in other lakes. The same is true of the benthics. The factors driving divergence between coexisting species are evidently repeatable, and thus the pattern (Fig. 2) cannot be due to chance. These limnetic and benthic species are also among the youngest on earth of any organism, since they occur exclusively in lakes that formed only 10–12,000 years ago, at the end of the last ice age. The pairs probably evolved from two separate invasions to lakes via the sea (Taylor and McPhail 1999, 2000). Coexisting limnetics and benthics are genetically different and reproductively isolated, so we consider them to be distinct species rather than morphs of a single species. However, low levels of gene flow still occur between them within each lake (Gow et al. 2006, 2007).
Testing the Coevolution Hypothesis
We used experiments to test several predictions of the coevolution hypothesis. The experiments were carried out in a series of ponds on the campus of the University of British Columbia (Fig. 3, photo on right). Each pond was 23 m × 23 m square with a maximum depth of 3 m in the center (Schluter 1994). They were constructed in 1991 and seeded with plants and invertebrates from one of the two-species lakes. The ponds were intended not to be identical to wild lakes but to mimic natural conditions sufficiently well to allow us to test predictions about natural processes. All invertebrates found in the diets of experimental fish were characteristic of the species in the wild. Fish predators of sticklebacks were absent (unless added as part of an experiment) but insect predators of young stickleback were abundant. In the experiments described herein, ponds were divided in two with a plastic membrane, and different treatments were applied to each half. All experiments were short-term, lasting 7–12 weeks within a single stickleback generation. Growth rate was used as a surrogate for fitness, measured by taking the natural log of fish body length (in millimeter) at the end of the experiment.
The first prediction tested was that divergence, if it had occurred by competition and coevolution, would have yielded lower competition between coexisting species over evolutionary time. To test this, we contrasted the amount of competition experienced by a zooplanktivorous stickleback (in this case the marine species) between two experimental treatments. In one treatment, the zooplanktivore was placed with the benthic species. This treatment represented the present day, two-species lake. In the other treatment, the zooplanktivore was placed with a solitary intermediate species. This treatment approximated the starting point of the stickleback species pairs in lakes, prior to divergence (Schluter and McPhail 1992; McPhail 1993). As predicted by the coevolution hypothesis, the growth rate of zooplanktivorous fish was higher in the benthic species treatment than in the solitary species treatment (Pritchard and Schluter 2001). Stickleback evidently compete for food, and the estimated strength of competition between coexisting species indeed declined after divergence.
The third prediction tested was that natural selection resulting from competition between species should be “frequency dependent.” In other words, natural selection pressures should change as the phenotype of the competitor changes. This is an important prediction of the coevolution hypothesis, which proposes that competition and natural selection continue to change as the competitors themselves evolve. The design of the experiment was similar to that of the previous study. In one treatment, the intermediate form was present with a limnetic species. In the other treatment, the intermediate form was present with a benthic species instead. The density of the intermediate form was the same between treatments, but this time total fish densities were also the same. What differed between treatments was the phenotype of the added competitor. As predicted by the coevolution hypothesis, natural selection in the intermediate form differed between treatments (Schluter 2003). In each case, the phenotypes closest to the added competitor felt the greatest impact (Fig. 4b; we are unable to say whether one competitor had a bigger impact than the other because this experiment didn’t include a third treatment in which the intermediate population was present alone). Natural selection arising from competition between species was indeed frequency-dependent.
These three experiments have strongly supported the hypothesis that the observed pattern, in which species are ecologically and phenotypically most different when they coexist (Fig. 3), is the evolutionary outcome of competition for resources. Morphologically more distant populations compete less than more similar forms (experiment 1). Competition from one species generates natural selection on another, favoring divergence (experiment 2). Natural selection arising from competition between species changes depending on the phenotypes of the competitors (experiment 3).
The consequences of resource competition between coexisting stickleback do not seem to end with divergence in habitat and resource use. One reason is that offshore and inshore environments also differ in the types of stickleback enemies, and stickleback have adapted to these differences. Stickleback are hunted by cutthroat trout (Oncorhynchus clarki) and diving birds such as loons (Gavia immer), which occur in virtually all the study lakes. These two types of predators are called “gape limited” because they swallow stickleback whole. In addition, young stickleback are preyed upon by insects, especially dragonfly nymphs (Aeshna) and backswimmers (Notonecta), which grab their prey and then chew or suck the fish rather than swallow them whole. Insects are mainly confined to the vegetation near the lake margins, and experiments in wading pools indicate that limnetics are more vulnerable than benthics there (Vamosi 2002). In contrast, the danger to stickleback swimming in open water is mainly from trout and diving birds, and experiments with cormorants suggest that benthics survive worse than limnetics in that environment (Vamosi 2002). Parasites are another source of mortality to stickleback, and the types of parasites also differ between benthics and limnetics (MacColl 2009a).
We’re not sure how predation and parasitism interacted with competition to yield divergence between coexisting species. One possibility is that competition was the main cause of divergence in habitat between limnetics and benthics, and that the habitat differences subsequently led to divergence in defensive traits. Under this view the importance of predation and parasitism is secondary to competition. The alternative hypothesis is that predation and parasitism were as vital as competition to divergence between stickleback in habitat, food, and other traits. Sorting out these two possibilities is challenging, but our understanding of the whole process of divergence is at stake. A couple of results so far favor the second of these two hypotheses.
First, solitary populations are not intermediate in armor between limnetics and benthics (Fig. 5), which is unexpected given that they are intermediate in habitat and diet. Instead, solitary stickleback have as much armor as the limnetic species of the two-species lakes. A plausible interpretation of this pattern is that the presence of the limnetic species reduces predation from gape-limited predators on the benthic species, allowing the evolution of reduced armor (Vamosi and Schluter 2004). This interpretation assumes that lakes with one and two stickleback species are not otherwise different in predation and parasitism, which has not been confirmed.
The second result comes from a pond experiment designed to test the effect of predation on competition and divergent selection (Rundle et al. 2003). The design of the experiment was similar to that of experiment 3 described in the previous section, except that we repeated both treatments in two groups of ponds. In one group of ponds, insect predators were depleted (but not eliminated) using traps and nets before the experiment was begun. In the second group of ponds, cutthroat trout and extra insect predators were added to increase total predation on stickleback. Not surprisingly, extra predation increased mortality and reduced (but did not eliminate) competition. Much more surprisingly, the strength of divergent natural selection between competitors was increased rather than diminished in ponds where mortality was high. This result seems paradoxical, but the strength of divergent selection is expected to depend not so much on how strong competition is, but rather on how rapidly competition declines between individuals as they differ more greatly in phenotype (Rundle et al. 2003). Abrams et al. (2008) has identified the conditions under which predation strengthens or weakens divergent selection from competition. In our experiment, at least, predation promoted divergence via competition.
Coevolution and Speciation
Finally, there is indication that coevolution has contributed to the process of stickleback speciation—the origin of the limnetic and benthic species pairs.
Speciation is defined as the evolution of reproductive isolation (reduced gene exchange) between populations (Coyne and Orr 2004).
An extraordinary aspects of the stickleback species pairs is their youth—they occur only in lakes that formed 10–12,000 years old. Like most very young species occurring together, limnetic and benthic stickleback species interbreed to a small degree, yet this has not caused their collapse under normal circumstances. Hybrids are selected against (Gow et al. 2007), and one reason is that they are morphologically intermediate and thus have a lower feeding efficiency and growth rate in both the inshore and offshore habitats compared with the limnetic and benthic species (Hatfield and Schluter 1999; Rundle 2002). Hybrids are at a competitive disadvantage. It is likely that this competitive disadvantage is greater today than earlier in the history of the species pairs, because each new adaptation in the benthic or limnetic species that improved its ability to exploit its preferred habitat would have further reduced the fitness of intermediate phenotypes, including hybrids. The implication is that competition and coevolution, by facilitating phenotypic divergence, have contributed to the reduction of gene flow between them and to their persistence over time.
This argument considers only the fate of hybrids, but in fact not many hybrids are formed because of behavioral differences between the species. Limnetics strongly prefer to mate with limnetics, and benthics mate almost exclusively with benthics. We now know that body size is one of the cues used by stickleback to identify and mate with their own type (Nagel and Schluter 1998). Size is a fairly effective cue because large, reproductively mature benthics hardly overlap the smaller limnetics in size. In this case, it is easy to see how natural selection, by favoring different body sizes in the inshore and offshore environments, would indirectly strengthen the tendency of limnetics to mate with limnetics, and benthics with benthics (Vines and Schluter 2006). This represents a second way in which competition, by favoring divergence, would contribute to reduced gene exchange. Such an influence of competition on speciation is something that Darwin (1859) foresaw, but for which evidence is only now beginning to emerge.
The threespine stickleback provides observational and experimental evidence for competition and coevolution in the divergence of coexisting species. Our studies of this system have also suggested that other interactions, such as predation and parasitism, have played an important part. Finally, there is evidence that divergent selection arising from these interactions has facilitated the very origin of species. The stickleback species pairs represent a powerful case study of the influence of coevolution on the generation of biodiversity.
Nevertheless, questions remain that continue to demand attention. One challenge is to connect measurements of natural selection on phenotypic traits to genetic changes underlying evolved differences between the species. Such studies are only now becoming feasible with the availability of complete genome sequences for stickleback (Kingsley et al. 2004), and with the identification of major genes and genomic regions underlying species differences. For example, knowing something about the genes will make it possible to carry out experimental studies to measure the effects of competition and other species interactions at the molecular level. For these reasons, research on the stickleback species pairs will continue to provide insights into the coevolutionary process.
All these efforts to understand the impacts of coevolution on divergence and speciation in stickleback would justify only mild curiosity if the results turned out to be unique to this system. However, intensive studies of young species in other groups of organisms including Anolis lizards on Caribbean islands (Losos 2009), spadefoot toad tadpoles in the American southwest (Pfennig and Murphy 2000), and Darwin's finches on Galápagos islands (Grant and Grant 2006), have uncovered similar mechanisms, suggesting that they occur widely (though not necessarily universally). Competition and coevolution are likely to be major drivers of species differentiation in nature. Without them, many closely related species would be more similar in ecology and phenotype, and the breadth of life’s diversity would likely be considerably less.
Our work was made possible by the discovery and early descriptions of the stickleback species pairs by Don McPhail and his students. I am also grateful to the University of British Columbia for supporting the experimental ponds facility. Thanks to John Thompson and Rodrigo Medel for the invitation to participate in this issue, and for their comments on the manuscript. My research is funded by the Natural Sciences and Engineering Research Council of Canada, the British Columbia Knowledge Development Fund, the Canada Foundation for Innovation, and the Canada Research Chairs.
- Abrams PA. Adaptive responses of predators to prey and prey to predators: the failure of the arms race analogy. Evolution. 1986a;40:1229–47.View ArticleGoogle Scholar
- Abrams PA. Character displacement and niche shift analyzed using consumer-resource models of competition. Theor Popul Biol. 1986b;29:107–60.View ArticleGoogle Scholar
- Abrams PA, Rueffler C, Kim G. Determinants of the strength of disruptive and/or divergent selection arising from resource competition. Evolution. 2008;62:1571–86.View ArticleGoogle Scholar
- Barrett RDH, Rogers SM, Schluter D. Environment specific pleiotropy facilitates divergence at the Ectodysplasin locus in threespine stickleback. Evolution. 2009;63:2831–7.View ArticleGoogle Scholar
- Brown Jr WL, Wilson EO. Character displacement. Syst Zool. 1956;5:49–64.View ArticleGoogle Scholar
- Coyne JA, Orr HA. Speciation. Sunderland: Sinauer Associates; 2004.Google Scholar
- Darwin C. On the origin of species by means of natural selection. London: John Murray; 1859.Google Scholar
- Doebeli M. An explicit genetic model for ecological character displacement. Ecology. 1996;77:510–20.View ArticleGoogle Scholar
- Gorbushin AM. The enigma of mud snail shell growth: asymmetrical competition or character displacement? Oikos. 1996;77:85–92.View ArticleGoogle Scholar
- Gow JL, Peichel CL, Taylor EB. Contrasting hybridization rates between sympatric three-spined sticklebacks highlight the fragility of reproductive barriers between evolutionarily young species. Mol Ecol. 2006;15:739–52.View ArticleGoogle Scholar
- Gow JL, Peichel CL, Taylor EB. Ecological selection against hybrids in natural populations of sympatric threespine sticklebacks. J Evol Biol. 2007;20:2173–80.View ArticleGoogle Scholar
- Grant PR. The classic case of character displacement. Evol Biol. 1975;8:237–337.Google Scholar
- Grant PR, Grant BR. Evolution of character displacement in Darwin's finches. Science. 2006;313:224–6.View ArticleGoogle Scholar
- Grant PR, Grant BR. How and why species multiply: the radiation of Darwin's finches. Princeton: Princeton University Press; 2008.Google Scholar
- Hatfield T, Schluter D. Ecological speciation in sticklebacks: environment-dependent hybrid fitness. Evolution. 1999;53:866–73.View ArticleGoogle Scholar
- Kingsley DM, Zhu BL, Osoegawa K, De Jong PJ, Schein J, Marra M, et al. New genomic tools for molecular studies of evolutionary change in threespine sticklebacks. Behaviour. 2004;141:1331–44.View ArticleGoogle Scholar
- Lack D. Darwin's finches. Cambridge: Cambridge University Press; 1947.Google Scholar
- Losos JB. Lizards in an evolutionary tree: the ecology of adaptive radiation in anoles. Berkeley: University of California Press; 2009.Google Scholar
- MacColl ADC. Parasite burdens differ between sympatric three-spined stickleback species. Ecography. 2009a;32:153–60.View ArticleGoogle Scholar
- Maccoll ADC. Parasites may contribute to ‘magic trait’ evolution in the adaptive radiation of three-spined sticklebacks, Gasterosteus aculeatus (Gasterosteiformes: Gasterosteidae). Biol J Linn Soc. 2009b;96:425–33.View ArticleGoogle Scholar
- Marchinko KB. Predation's role in repeated phenotypic and genetic divergence of armor in threespine stickleback. Evolution. 2009;63:127–38.View ArticleGoogle Scholar
- Marchinko KB, Schluter D. Parallel evolution by correlated response: lateral plate reduction in threespine stickleback. Evolution. 2007;61:1084–90.View ArticleGoogle Scholar
- McPhail JD. Ecology and evolution of sympatric sticklebacks (Gasterosteus): origin of the species pairs. Can J Zool. 1993;71:515–23.View ArticleGoogle Scholar
- Nagel L, Schluter D. Body size, natural selection, and speciation in sticklebacks. Evolution. 1998;52:209–18.View ArticleGoogle Scholar
- Pfennig DW, Murphy PJ. Character displacement in polyphenic tadpoles. Evolution. 2000;54:1738–49.View ArticleGoogle Scholar
- Pritchard JR, Schluter D. Declining interspecific competition during character displacement: summoning the ghost of competition past. Evol Ecol Res. 2001;3:209–20.Google Scholar
- Reimchen TE. Spine deficiency and polymorphism in a population of Gasterosteus aculeatus: an adaptation to predators? Can J Zool (Revue Canadienne De Zoologie). 1980;58:1232–44.View ArticleGoogle Scholar
- Reimchen TE. Injuries on stickleback from attacks by a toothed predator (Oncorhynchus) and implications for the evolution of lateral plates. Evolution. 1992;46:1224–30.View ArticleGoogle Scholar
- Reimchen TE. Predator handling failures of lateral plate morphs in Gasterosteus aculeatus: Functional implications for the ancestral plate condition. Behaviour. 2000;137:1081–96.View ArticleGoogle Scholar
- Rundle HD. A test of ecologically dependent postmating isolation between sympatric sticklebacks. Evolution. 2002;56:322–9.View ArticleGoogle Scholar
- Rundle HD, Vamosi SM, Schluter D. Experimental test of predation's effect on divergent selection during character displacement in sticklebacks. Proc Natl Acad Sci USA. 2003;100:14943–8.PubMed CentralView ArticleGoogle Scholar
- Schluter D. Adaptive radiation in sticklebacks: size, shape, and habitat use efficiency. Ecology. 1993;74:699–709.View ArticleGoogle Scholar
- Schluter D. Experimental evidence that competition promotes divergence in adaptive radiation. Science. 1994;266:798–801.View ArticleGoogle Scholar
- Schluter D. Adaptive radiation in sticklebacks: trade-offs in feeding performance and growth. Ecology. 1995;76:82–90.View ArticleGoogle Scholar
- Schluter D. The ecology of adaptive radiation. Oxford: Oxford University Press; 2000.Google Scholar
- Schluter D. Frequency dependent natural selection during character displacement in sticklebacks. Evolution. 2003;57:1142–50.View ArticleGoogle Scholar
- Schluter D, McPhail JD. Ecological character displacement and speciation in sticklebacks. Am Nat. 1992;140:85–108.View ArticleGoogle Scholar
- Taper ML, Case TJ. Quantitative genetic models for the coevolution of character displacement. Ecology. 1985;66:355–71.View ArticleGoogle Scholar
- Taylor EB, McPhail JD. Evolutionary history of an adaptive radiation in species pairs of threespine sticklebacks (Gasterosteus): insights from mitochondrial DNA. Biol J Linn Soc. 1999;66:271–91.View ArticleGoogle Scholar
- Taylor EB, McPhail JD. Historical contingency and ecological determinism interact to prime speciation in sticklebacks, Gasterosteus. Proc R Soc Lond B. 2000;267:2375–84.View ArticleGoogle Scholar
- Thompson JN. The geographic mosaic of coevolution. Chicago: University of Chicago Press; 2005.Google Scholar
- Vamosi SM. Predation sharpens the adaptive peaks: survival trade-offs in sympatric sticklebacks. Ann Zool Fenn. 2002;39:237–48.Google Scholar
- Vamosi SM, Schluter D. Character shifts in the defensive armor of sympatric sticklebacks. Evolution. 2004;58:376–85.View ArticleGoogle Scholar
- Vines TH, Schluter D. Strong assortative mating between allopatric sticklebacks as a by-product of adaptation to different environments. Proc R Soc Lond B. 2006;273:911–6.View ArticleGoogle Scholar