To examine how genetic variation in a plant population affects arthropod community richness and composition, we quantified the arthropod communities on a synthetic population of Eucalyptus amygdalina, E. risdonii, and their F1 and advanced‐generation hybrids. Five major patterns emerged. First, the pure species and hybrid populations supported significantly different communities. Second, species richness was significantly greatest on hybrids (F1 > F2 > E. amygdalina > E. risdonii). These results are similar to those from a wild population of the same species and represent the first case in which both synthetic and wild population studies confirm a genetic component to community structure. Hybrids also acted as centers of biodiversity by accumulating both the common and specialist taxa of both parental species (100% in the wild and 80% in the synthetic population). Third, species richness was significantly greater on F1s than the single F2 family, suggesting that the increased insect abundance on hybrids may not be caused by the breakup of coadapted gene complexes. Fourth, specialist arthropod taxa were most likely to show a dominance response to F1 hybrids, whereas generalist taxa exhibited a susceptible response. Fifth, in an analysis of 31 leaf terpenoids that are thought to play a role in plant defense, hybrids were generally intermediate to the parental chemotypes. Within the single F2 family, we found significant associations between the communities of individual trees and five individual oil components, including oil yield, demonstrating that there is a genetic effect on plant defensive chemistry that, in turn, may affect community structure. These studies argue that hybridization has important community‐level consequences and that the genetic variation present in hybrid zones can be used to explore the genetic‐based mechanisms that structure communities.
Plant hybrid zones are dynamic centers of ecological and evolutionary processes for plants and their associated communities. Studies in the wild and in gardens with synthetic crosses showed that hybrid eucalypts supported the greatest species richness and abundances of insect and fungal taxa. In an updated review of 152 case studies of taxa associated with diverse hybridizing systems, there were 43 (28%) cases of hybrids being more susceptible than their parent species, 7 (5%) resistant, 35 (23%) additive, 35 (23%) dominant, and 32 (21%) showed no response to hybridization. Thus, most taxa respond to hybrids in ways that result in equal or greater abundance, and hybrids tend to accumulate the taxa of their parent species. These studies suggest that genetic‐based plant traits affect the distribution of many species and that the variation in hybrids can be used as tools to examine the genetic components of community structure and biodiversity. Several patterns have emerged thus far. (1) Genetic variation between classes of hybrids (e.g., F1’s vs. backcrosses) may equal or even exceed that found between species. (2) As a reflection of this genetic variation, herbivores are more likely to differentiate between hybrid classes than they are to differentiate between pure plant species. (3) The communities associated with different hybrid classes can differ from one another as well as from their parental species. (4) Generalist and specialist herbivores predictably vary in their responses to hybrids. (5) Plant hybrid zones may represent essential habitat for some arthropod species. (6) Even nesting birds respond to hybridizing plants. (7) Including multiple trophic levels and taxa from microbes to vertebrates, susceptible hybrid genotypes support greater biodiversity than resistant genotypes. (8) The effects of hybridization on common or keystone species can either positively or negatively affect biodiversity. The indirect impacts of hybridization on biodiversity may exceed the direct impacts and may result in “apparent” herbivore resistance or susceptibility at the community level. (9) Although hybrids are often maligned, exotic or problem hybrids generally result from human disturbances, whereas native hybrids are part of natural ecosystems and should be conserved. Three predictions are made: (1) Intermediate genetic differences between the parental species will result in the greatest genetic variation in the hybrid zone, which in turn will have a positive effect on biodiversity. (2) Bidirectional introgression enhances species richness on hybrids, whereas F1 sterility and unidirectional introgression limit the accumulation of species on hybrids. (3) Although susceptible hybrids are likely to support the greatest biodiversity, the impacts of hybridization on keystone species will be crucial in determining the overall effect.
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