Although sexual interactions between species (reproductive interference) have been reported from a wide range of animal taxa, their potential for determining species coexistence is often disregarded. Here, we review evidence from laboratory and field studies illustrating that heterospecific sexual interactions are frequently associated with fitness loss and can have severe ecological and evolutionary consequences. We define reproductive interference as any kind of interspecific interaction during the process of mate acquisition that adversely affects the fitness of at least one of the species involved and that is caused by incomplete species recognition. We distinguish seven types of reproductive interference: signal jamming, heterospecific rivalry, misdirected courtship, heterospecific mating attempts, erroneous female choice, heterospecific mating, and hybridization. We then discuss the sex-specific costs of these types and highlight two typical features of reproductive interference: density-dependence and asymmetry. Similar to competition, reproductive interference can lead to displacement of one species (sexual exclusion), spatial, temporal, or habitat segregation, changes in life history parameters, and reproductive character displacement. In many cases, patterns of coexistence might be shaped by reproductive interference rather than by resource competition, as the presence of a few heterospecifics might substantially decrease reproductive success. Therefore, interspecific sexual interactions should receive more attention in ecological research. Reproductive interference has mainly been discussed in the context of invasive species or hybrid zones, whereas its influence on naturally-occurring sympatric species pairs has rarely been addressed. To improve our knowledge of the ecological significance of reproductive interference, findings from laboratory experiments should be validated in the field. Future studies should also focus on ecological mechanisms, such as temporal spatial, or habitat partitioning, that might enable sexually interacting species to coexist. Reproductive interference also has implications for the management of endangered species, which can be threatened by sexual interactions with invasive or common species. Studies of reproductive interference might even provide new insights for biological pest control.
Summary 1.As species are often considered discrete natural units, interspecific sexual interactions are often disregarded as potential factors determining community composition. Nevertheless reproductive interference, ranging from signal jamming to hybridization, can have significant costs for species sharing similar signal channels. 2. We combined laboratory and field experiments to test whether the coexistence of two congeneric ground-hopper species with overlapping ranges might be influenced by sexual interactions. 3. In the laboratory experiment the number of conspecific copulations of Tetrix ceperoi decreased substantially in the presence of Tetrix subulata . Males of T. ceperoi performed more mating attempts with heterospecific females, whereas females of T. subulata rejected these heterospecific approaches more often than those of conspecifics. Although no heterospecific matings occurred in the laboratory, the reproductive success of T. ceperoi was reduced substantially in field experiments. Negative effects on T. subulata were found only at high densities. 4. Our results suggest that reproductive interference could have similar consequences as competition, such as demographic displacement of one species ('sexual exclusion'). As reproductive interference should be selected against, it may also drive the evolution of signals (reproductive character displacement) or promote habitat, spatial or temporal segregation.
Similar to resource competition, reproductive interference may hamper the coexistence of closely related species. Species that utilize similar signal channels during mate finding may face substantial fitness costs when they come into contact and demographic displacement of the inferior species (sexual exclusion) is a likely outcome of such interactions. The two ground-hopper species Tetrix ceperoi and Tetrix subulata broadly overlap in their ranges and general habitat requirements, but rarely co-occur on a local scale. Results from laboratory and field experiments suggest that this mosaic pattern of sympatry might be influenced by reproductive interference. Here, we examine the significance of sexual interactions for these species in the field and test hypotheses on mechanisms of coexistence. Our results show that heterospecific sexual interactions also occur under field conditions, but in contrast to the experiments T. ceperoi was not the inferior species. The number of male mating attempts of both species was strongly correlated with encounter frequencies. Males discriminated between the sexes but not between the species, suggesting an incomplete mate recognition system in both species. The analysis of microhabitat preferences and spatial distribution revealed that habitat partitioning is not a suitable mechanism of coexistence in this system. Instead, the costs of reproductive interference are substantially mitigated by different niche breadths leading to different degrees of aggregation. Despite a considerable niche overlap T. ceperoi displayed a stronger preference for bare ground and occurred more aggregated than T. subulata , which had a broader niche. These differences may reduce the frequencies of heterospecific encounters and interactions in the field. Our results demonstrate that coexistence in the presence of reproductive interference is comparable to resource competition, being strongly influenced by ecological traits of the involved species, such as niche breadth and dispersion pattern.
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The question of how phenotypic variation is maintained within populations has long been a central issue in evolutionary biology. Most of these studies focused on the maintenance of genetic variability, but the phenotype of organisms may also be influenced by environmental cues experienced during ontogeny. Color polymorphism has received particular attention in evolutionary studies as it has strong fitness consequences. However, if body coloration is influenced by the environment, any conclusions on evolutionary consequences of fitness trade-offs can be misleading. Here we present data from a laboratory experiment on the influence of substrate color on three aspects of the coloration of two ground-hopper species, Tetrix subulata and Tetrix ceperoi. We reared hatchlings either on dark or on light substrates, using a split-brood design. Although the type of pronotal pattern changed mainly in response to nymphal development, the basic color was strongly influenced by the substrate color. In both species, black and dark olive color morphs were found more frequently on the dark substrate, whereas the gray color morph dominated on the light substrate. These findings have considerable implications for our understanding of color morph evolution as they show that color polymorphism may not only be maintained by natural selection acting on discrete color morphs, but also by phenotypic plasticity, which enables organisms to adjust to the environmental conditions experienced during ontogeny. This facultative morphology is opposing to the prevailing view of color morph adaptation, which assumes a purely genetic determination and co-evolution of discrete color morphs with life history traits.
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