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Raia et al. propose that the evolution of the shape and complexity of animal ornaments (e.g., deer antlers) can be explained by interspecific variation in body size and is not influenced by sexual selection. They claim to show that ornament complexity is related to body size by an 0.25-power law and argue that this finding precludes a role for sexual selection in the evolution of ornament complexity. However, their study does not test alternative hypotheses and mismeasures antler shape allometry by omitting much of the published data. We show that an index of sexual selection (sexual size dimorphism) is positively correlated with size-corrected antler complexity and that the allometric slope of complexity is substantially greater than 0.25, contra Raia et al. We conclude that sexual selection and physical constraints both affect the evolution of antler shape. [ABSTRACT FROM AUTHOR]

Mate choice is a common feature of sexually reproducing species. In sessile or sedentary external fertilizers, however, direct interactions between reproductive partners are minimal, and instead mate recognition and choice must occur at the level of gametes. It is common for some sperm and egg combinations to have higher fertilization success than others, but it remains unclear whether differences in fertilization reflect gamete-level mate choice (GMC) for paternal quality or parental compatibility. Here, we examine the mechanisms underlying GMC in an externally fertilizing ascidian. A manipulative mate-choice assay confirmed that offspring viability was greater in clutches where we allowed GMC than in clutches where we precluded GMC. A complementary quantitative genetic experiment then revealed that paternal quality effects were generally weaker than parental compatibility effects, particularly for the trait combination underlying the benefits of GMC. Overall, our data suggest that gametes that are more compatible at fertilization produce more viable offspring than gametes that are less compatible at fertilization. Therefore, although the regalia we typically associate with sexual selection are absent in external fertilizers, mechanisms that allow females to bias fertilization in favor of some males over others produce significant fitness benefits in organisms reproducing via the ancestral strategy. [ABSTRACT FROM AUTHOR]

Environments that vary within a generation of an organism provide opportunities for adaptation if the level of variation is severe and predictable. We describe a model of evolution in such environments with genotypes that show trade-offs in viability and fecundity. One genotype develops rapidly and has superior viability but reduced fertility relative to the alternative genotype. Conditions that allow the evolution of the rapidly developing genotypes are explored. We show how the evolution of ovoviviparity and resource specialization in Drosophila sechellia shares many important features of this model. We suggest that our model may capture many of the evolutionary forces responsible for the evolution of niche specialization and ovoviviparity seen in D. sechellia. [ABSTRACT FROM AUTHOR]

Selection on naturally occurring hybrid individuals is a key component of speciation theory, but few studies examine the functional basis of hybrid performance. We examine the functional consequences of hybridization in nature, using the freshwater sunfishes (Centrarchidae), where natural hybrids have been studied for more than a century and a half. We examined bluegill (Lepomis macrochirus), green sunfish (Lepomis cyanellus), and their naturally occurring hybrid, using prey-capture kinematics and morphology to parameterize suction-feeding simulations on divergent parental resources. Hybrid individuals exhibited kinematics intermediate between those of the two parental species. However, performance assays indicated that hybrids display performance most similar to the worse-performing species for a given parental resource. Our results show that intermediate hybrid phenotypes can be impaired by a lessthan- intermediate performance and hence suffer a larger loss in fitness than could be inferred from morphology alone. [ABSTRACT FROM AUTHOR]

Luxuriant, bushy antlers, bizarre crests, and huge, twisting horns and tusks are conventionally understood as products of sexual selection. This view stems from both direct observation and from the empirical finding that the size of these structures grows faster than body size (i.e., ornament size shows positive allometry).We contend that the familiar evolutionary increase in the complexity of ornaments over time in many animal clades is decoupled from ornament size evolution. Increased body size comes with extended growth. Since growth scales to the quarter power of body size, we predicted that ornament complexity should scale according to the quarter power law as well, irrespective of the role of sexual selection in the evolution and function of the ornament. To test this hypothesis, we selected three clades (ammonites, deer, and ceratopsian dinosaurs) whose species bore ornaments that differ in terms of the importance of sexual selection to their evolution.We found that the exponent of the regression of ornament complexity to body size is the same for the three groups and is statistically indistinguishable from0.25.We suggest that the evolution of ornament complexity is a by-product of Cope's rule. We argue that although sexual selection may control size in most ornaments, it does not influence their shape. [ABSTRACT FROM AUTHOR]

The evolution of convergent phenotypes in lineages subject to similar selective pressures is a common feature of adaptive radiation. In geographically replicated radiations, repeated convergence occurs between clades occupying distinct regions or islands. Alternatively, a clade may repeatedly reach the same adaptive peaks in broadscale sympatry, resulting in extensive convergence within a region. Rockfish (Sebastes sp.) have radiated in both the northeast and northwest Pacific, allowing tests of the extent and geographic pattern of convergence in a marine environment. We used a suite of phylogenetically informed methods to test for morphological convergence in rockfish. We examined patterns of faunal similarity using nearest neighbor distances in morphospace and the frequency of morphologically similar yet distantly related species pairs. The extent of convergence both between regions and within the northeast Pacific exceeds the expectation under a Brownian motion null model, although constraints on trait space could account for the similarity. We then used a recently developed method (SURFACE) to identify adaptive peak shifts in Sebastes evolutionary history. We found that the majority of convergent peak shifts occur within the northeast Pacific rather than between regions and that the signal of peak shifts is strongest for traits related to trophic morphology. Pacific rockfish thus demonstrate a tendency toward morphological convergence within one of the two broad geographic regions in which they have diversified. [ABSTRACT FROM AUTHOR]

Traits that increase mating success in males may come at a cost, such as an increased risk of predation. However, predatormediated selection is challenging to document in natural populations, hampering our understanding of the trade-offs between sexual selection and predation. Here we report on a study of predator- mediated natural selection on wing traits in the damselfly Calopteryx splendens, the males of which possess conspicuous wing patches. Wagtails (genus Motacilla) are important avian predators of C. splendens, capturing them in flight and removing the wings prior to consumption. Using geometric morphometric techniques, we quantified the strength and mode of selection on wing traits by comparing wings from depredated individuals with the standing variation present in the population. Our results reveal that predator- mediated selection is stronger on secondary sexual characters than on size and shape, suggesting that traits related to flight performance are closer to their adaptive peaks. This could be a consequence of the long-term evolutionary association with avian predators, whereas stronger selection on conspicuous secondary sexual traits may reflect trade-offs between sexual and natural selection. Finally, even though C. splendens possesses nearly identical fore- and hindwings, we found evidence for divergent selection between them. [ABSTRACT FROM AUTHOR]

Our knowledge about how the environment influences sexual selection regimes and how ecology and sexual selection interact is still limited. We performed an integrative study of wing pigmentation in calopterygid damselflies, combining phylogenetic comparative analyses, field observations and experiments. We investigated the evolutionary consequences of wing pigmentation for sexual dimorphism, speciation, and extinction and addressed the possible thermoregulatory benefits of pigmentation. First, we reconstructed ancestral states of male and female phenotypes and traced the evolutionary change of wing pigmentation. Clear wings are the ancestral state and that pigmentation dimorphism is derived, suggesting that sexual selection results in sexual dimorphism. We further demonstrate that pigmentation elevates speciation and extinction rates. We also document a significant biogeographic association with pigmented species primarily occupying northern temperate regions with cooler climates. Field observations and experiments on two temperate sympatric species suggest a link between pigmentation, thermoregulation, and sexual selection, although body temperature is also affected by other phenotypic traits such as body mass, microhabitat selection, and thermoregulatory behaviors. Taken together, our results suggest an important role for wing pigmentation in sexual selection in males and in speciation. Wing pigmentation might not increase ecological adaptation and species longevity, and its primary function is in sexual signaling and species recognition. [ABSTRACT FROM AUTHOR]

The biomass of living organisms hosts oniy a small portion of the elemental abundance at the surface of the Earth, yet biology plays a defining role in the composition and stability of the biosphere by acting on sensitive geochemical feedbacks controlling global element cycles. This type of influence is evident in a class of evolutionary innovations that have a profoundly disproportionate effect on the biosphere, referred to here as evolutionary innovation biospheric feedbacks (EIBFs). A particular biological innovation need not be complex, rather its influence is amplified by its effect on geochemical feedbacks controlling elemental cycling. The lead-up to the metazoan radiation (~585 million years ago) provides an example of such an EIBF. While commonly attributed to an increase in free oxygen concentration, the reason for this step increase in O2 almost 2 billion years after the advent of oxygenic photosynthesis is traced to a seemingly unrelated evolutionary innovation resulting in a critical by-product of the first soils: secondary clay minerals. Detrital clay minerals deposited in continental margin sediments sequester organic carbon compounds and thus prevent consumption ofatmospheric oxygen produced during photosynthesis. The transition from the abiotic to biotic land surface at the end of the Precambrian shifted biogeochemical cycling to this terrestrial-dominated modern mode that enabled sufficient oxygenation of the biosphere to trigger the metazoan radiation. [ABSTRACT FROM AUTHOR]

Density-dependent selection is one of earliest topics of joint interest to both ecologists and evolutionary biologists and thus occupies an important position in the histories of these disciplines. This joint interest is driven by the fact that density-dependent selection is the simplest form of feedback between an ecological effect of an organism's own making (crowding due to sustained population growth) and the selective response to the resulting conditions. This makes density-dependent selection perhaps the simplest process through which we see the full reciprocity between ecology and evolution. In this article, we begin by tracing the history of studying the reciprocity between ecology and evolution, which we see as combining the questions of evolutionary ecology with the assumptions and approaches of ecological genetics. In particular, density-dependent fitness and density-dependent selection were critical concepts underlying ideas about adaptation to biotic selection pressures and the coadaptation of interacting species. However, theory points to a critical distinction between density-dependent fitness and densitydependent selection in their influences on complex evolutionary and ecological interactions among coexisting species. Although densitydependent fitness is manifestly evident in empirical studies, evidence of density-dependent selection is much less common. This leads to the larger question of how prevalent and important density-dependent selection might really be. Life-history variation in the least kulifish Heterandria formosa appears to reflect the action of densitydependent selection, and yet compelling evidence is elusive, even in this well-studied system, which suggests some important challenges for understanding density-driven feedbacks between ecology and evolution. [ABSTRACT FROM AUTHOR]

Living nature Can be thought of as a tapestry, defined not only by its constituent parts but also by bow these parts are woven together. The weaving of this tapestry is a metaphor for species interactions, which can be divided into three broad classes: competitive, mutualistic, and consumptive. Direct interactions link together as more complex networks, for example, the joining of consumptive interactions into food webs. Food web dynamics are driven, in turn, by changes in the abundances of seeb members, whose numbers or biomass respond to bottom-up (resource limitation) and topdown (consumer limitation) forcing. The relative strengths of topdosen and bottom-up forcing on the abundance of a given web member depend on its ecological context, including its topological position ieithin the food web. Top-down effects by diverse consumers are nearly ubiquitous, in many cases influencing the structure and operation of ecosystems. While the ecological effects of such interactions are seell known, far less is knosen of their evolutionary consequences. In this essay, we describe sundry consequences of these interaction chains on species and ecosystem processes, explain several knosvn or suspected evolutionary effects of consumer-induced interaction chains, and identified areas where reciprocity between ecology and evolution involving the indirect effects of consumer-prey interaction chains might be further explored. [ABSTRACT FROM AUTHOR]

The extent to which evolutionary change occurs in a predictable manner under field conditions and how evolutionary changes feed back to influence ecological dynamics are fundamental, yet unresolved, questions. To address these issues, we established eight replicate populations of native common evening primrose (Oenothera biennis). Each population was planted with 18 genotypes in identical frequency. By tracking genotype frequencies with microsatellite DNA markers over the subsequent three years (up to three generations, ≈5,000 genotyped plants), we show rapid and consistent evolution of two heritable plant life-history traits (shorter life span and later flowering time). This rapid evolution was only partially the result of differential seed production; genotypic variation in seed germination also contributed to the observed evolutionary response. Since evening primrose genotypes exhibited heritable variation for resistance to insect herbivores, which was related to flowering time, we predicted that evolutionary changes in genotype frequencies would feed back to influence populations of a seed predator moth that specializes on 0. biennis. By the conclusion of the experiment, variation in the genotypic composition among our eight replicate field populations was highly predictive of moth abundance. These results demonstrate how rapid evolution in field populations of a native plant can influence ecological interactions. [ABSTRACT FROM AUTHOR]

Herbivores are credited with driving the evolutionary diversification of plant defensive strategies over macroevolutionary time. For this to be true, herbivores must also cause short-term evolution within plant populations, but few studies have experimentally tested this prediction. We addressed this gap using a longterm manipulative field experiment where exclosures protected 22 plant populations from natural rabbit herbivory for <1 to 26 years. We collected seeds of Rumex acetosa L. (Polygonaceae) from our plots and grew them in a common greenhouse environment to quantify evolved differences among populations in individual plant growth rate, tolerance to herbivory, competitive ability, and the concentration of secondary metabolites (tanninS and oxalate) implicated in defense against herbivores. In 26 years without rabbit herbivory, plant growth rate decreased linearly by 30%. We argue that plant growth rate has evolved as a defense against intense rabbit herbivory. In contrast, we found no change in tolerance to herbivory or concentrations of secondary metabolites. We also found no change in competitive ability, suggesting that contemporary evolution may not feed back to alter ecological interactions within this plant community. Our results combined with those of other studies show that the evolution of gross morphological traits such as growth rate in response to herbivory may be common, which calls into question assumptions about some of the most popular theories of plant defense. [ABSTRACT FROM AUTHOR]

In proposing his genetic feedback mechanism, David Pimentel was one of the first biologists to argue that the reciprocal interplay of ecological and evolutionary dynamics is an important process regulating population dynamics and ultimately affecting community composition. Although the past decade has seen an increase in research activity on these so-called eco-evolutionary dynamics, there remains a conspicuous lack of compelling natural examples of such feedback. Here we argue that this lack may be due to an inherent difficulty in detecting eco-evolutionary dynamics in nature. By examining models of virulence evolution, host resistance evolution, and antigenic evolution, we show that the influence of evolution on ecological dynamics can often be obscured by other ecological processes that yield similar dynamics. We then show, however, that mechanistic models can be used to navigate this, in Pimentel's words, "devious" course of evolution when effectively combined with empirical data. We argue that these models, improving upon Pimentel's original mathematical models, svill therefore play an increasingly important role in identifying more subtle, but possibly ubiquitous, eco-evolutionary dynamics in nature. To highlight the importance of identifying these potentially subtle dynamics in nature, we end by considering our ability to anticipate the effect of population control strategies in the presence of these eco-evolutionary feedbacks. [ABSTRACT FROM AUTHOR]

Conventional wisdom holds that the complex shapes of deer antlers are produced under the sole influence of sexual selection. We questioned this view by demonstrating that trends for increased body size evolution passively yield more-complex ornaments, even in organisms where no effect of sexual selection is possible, with similar allometric slopes. Recent investigations suggest that sexual selection on antlers of larger deer species is stronger than that in smaller species; hence, the use of conspicuous antlers for display in large male deer is a secondary function driven by especially intense sexual selection on these large-bodied species. Since ancestral deer were small and had very simple antlers, such an intense selection on antlers shape was probably absent in early deer. Therefore, the evolution of complex ornaments is coupled with body size evolution, even in deer. [ABSTRACT FROM AUTHOR]