Given the importance of Roseobacters in biogeochemical cycles of the ocean, their well-characterized genome sequences [6] within a clade, and global abundance, the marine Roseobacter clade is ideal for elucidating bacterial diversification and adaptation to ocean environments.
In such instances, opportunities for physical isolation in distinct environments provide ideal conditions that promote intraspecific diversification.
Monogeneans, a group of mostly ectoparasitic flatworms predominantly found in fishes, seem to be an ideal model for investigating parasite diversification for at least three reasons.
The high numbers of species found within the Rift Valley's lakes and rivers, as well as the impressive degree of phenotypic variation present among closely related species, make these fishes ideal for studies on functional diversification and speciation.
Furthermore, this early-stage diversification strategy is not ideal for library synthesis.
The Malagasy lemurs are a spectacular example of adaptive radiation and provide an ideal model for studies of evolutionary diversification [ 23].
The scleractinian coral S. hystrix represents an ideal candidate to examine processes of ecological diversification and local adaptation in corals, as it occurs in most habitats [55], and is geographically widespread [26].
Nevertheless, such diversification analyses would be the ideal new direction to explore in further studies that aim to detect a link between high rates of diversification and morphological adaptations to an arid environment in ice plants.
This parallel evolutionary transition in the two species of EA-ENA disjunct distribution suggests an ideal group to address the causes of diversification in breeding systems.
Given the evidence regarding plant HSP20s and their functional diversification, these proteins are considered ideal targets for improving the development of new varieties of soybean that are tolerant to a wide range of stress conditions or combinations of these stresses.
