Mutualistic microalgae co-diversify with reef corals that acquire symbionts during egg development
Mutualistic microalgae co-diversify with reef corals that acquire symbionts during egg development
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DOI:
10.1038/s41396-021-01007-8
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发表时间:
2021-05
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通讯作者:
Kira E. Turnham;D. Wham;E. Sampayo;T. Lajeunesse
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作者:
Kira E. Turnham;D. Wham;E. Sampayo;T. Lajeunesse
The application of molecular genetics has reinvigorated and improved how species are defined and investigated scientifically, especially for morphologically cryptic micro-organisms. Here we show how species recognition improves understanding of the ecology and evolution of mutualisms between reef-building corals and their mutualistic dinoflagellates (i.e. Symbiodiniaceae). A combination of genetic, ecological, and morphological evidence defines two sibling species ofCladocopium(formerlySymbiodiniumClade C), specific only to host corals in the common genusPocillopora, which transmit their obligate symbionts during oogenesis.Cladocopium latusorumsp. nov. is symbiotic withP. grandis/meandrinawhile the smaller-celledC. pacificumsp. nov. associates withP. verrucosa. Both symbiont species form mutualisms withPocilloporathat brood their young. Populations of each species, like their hosts, are genetically well connected across the tropical and subtropical Pacific Ocean, indicating a capacity for long-range dispersal. A molecular clock approximates their speciation during the late Pliocene or early Pleistocene as Earth underwent cycles of precipitous cooling and warming; and corresponds to when their hosts were also diversifying. The long temporal and spatial maintenance of high host fidelity, as well as genetic connectivity across thousands of kilometers, indicates that distinct ecological attributes and close evolutionary histories will restrain the adaptive responses of corals and their specialized symbionts to rapid climate warming.