Can plant-fungal symbioses underpin plant diversity?
Lead Research Organisation:
Imperial College London
Department Name: Life Sciences
Abstract
Our understanding of how species originate (speciation) has changed considerably since Darwin's seminal work. One aspect, however, that has been ignored is the role that microbes can play in driving speciation. Here, we propose a new mechanism for the origin of species, whereby coevolutionary divergence in plant-mycorrhizal associations increases local adaptation and leads to the completion of speciation, using one of the most compelling examples of speciation in the face of gene flow as our model system: The Howea palms of Lord Howe Island. While it is well known that species can diverge due to geographic barriers such as mountain ridges or oceans, populations can also split in the face of gene flow without geographic isolation, for example through specialisation to habitats or resources. In this context, symbiotic associations that plants have with microbes may be particularly powerful in simultaneously facilitating local adaptation and reproductive isolation leading to speciation.
We will focus on two sister species of palms (Howea), endemic to Lord Howe Island, a remote island in the Tasman sea, and their interactions with arbuscular mycorrhizal fungi. Howea palms represent the dominant vegetation on the island. The speciation scenario for Howea involves adaptation to different soils, volcanic rocks and calcareous deposits, and associated fitness trade-offs. We hypothesise that soil and soil microbes have affected local adaptation of the ancestral palm population, which in turn led to differences in flowering time, and ultimately promoted speciation. Differing levels of mycorrhizal colonisation and gene expression co-regulated in Howea and mycorrhizal associations may have led to the emergence of distinct forms of Howea populations occupying different soils. We will test these key hypotheses using metagenomics and RNA-seq combined with long-term field experiments on Lord Howe Island.
The proposed work has the potential to bring drastic rethinking about the mechanisms of speciation and how coevolution contributes to species divergence. The proposed work will unravel some of the most neglected hypotheses in evolution, such as how microbes can drive plant speciation, and hence the link between microbiome and plant diversity. Given the widespread nature of plant-mycorrhizal symbioses, their importance in crop production, and the prominence of soil and plant diversity in ecosystem functioning, our research will also have far-reaching impact in applied ecology and agriculture, beyond evolutionary biology.
We will focus on two sister species of palms (Howea), endemic to Lord Howe Island, a remote island in the Tasman sea, and their interactions with arbuscular mycorrhizal fungi. Howea palms represent the dominant vegetation on the island. The speciation scenario for Howea involves adaptation to different soils, volcanic rocks and calcareous deposits, and associated fitness trade-offs. We hypothesise that soil and soil microbes have affected local adaptation of the ancestral palm population, which in turn led to differences in flowering time, and ultimately promoted speciation. Differing levels of mycorrhizal colonisation and gene expression co-regulated in Howea and mycorrhizal associations may have led to the emergence of distinct forms of Howea populations occupying different soils. We will test these key hypotheses using metagenomics and RNA-seq combined with long-term field experiments on Lord Howe Island.
The proposed work has the potential to bring drastic rethinking about the mechanisms of speciation and how coevolution contributes to species divergence. The proposed work will unravel some of the most neglected hypotheses in evolution, such as how microbes can drive plant speciation, and hence the link between microbiome and plant diversity. Given the widespread nature of plant-mycorrhizal symbioses, their importance in crop production, and the prominence of soil and plant diversity in ecosystem functioning, our research will also have far-reaching impact in applied ecology and agriculture, beyond evolutionary biology.
