Evolutionary radiation and microbial community dynamics shape the thermal tolerance of Fungiidae in the southern South China Sea

Author:

Wei Yuxin1ORCID,Chen Biao1ORCID,Yu Kefu12,Liao Zhiheng3,Yu Xiaopeng1,Qin Zhenjun1,Bao Zeming1,Xu Lijia4,Wang Yongzhi4

Affiliation:

1. Guangxi Laboratory on the Study of Coral Reefs in the South China Sea, Coral Reef Research Center of China, School of Marine Sciences, Guangxi University, Nanning, China

2. Southern Marine Science and Engineering Guangdong Laboratory, Guangzhou, China

3. Key Laboratory of Environmental Change and Resource Use in Beibu Gulf, Ministry of Education, Nanning Normal University, Nanning, China

4. South China Institute of Environmental Sciences, MEE, Guangzhou, China

Abstract

ABSTRACT Fungiidae have shown increased thermal adaptability in coral reef ecosystems under global warming. This study analyzes the evolutionary divergence and microbial communities of Fungiidae in the Sanjiao Reef of the southern South China Sea and explores the impact of coral evolution radiation and microbial dynamics on the heat tolerance of Fungiidae. The results found that Cycloseris was an ancient branch of Fungiidae, dating back approximately 147.8953 Mya, and Fungiidae differentiated into two ancestral clades (clades I and II) before 107.0312 Ma. Fungiidae exhibited specific symbioses with the Cladocopium C27 sub-clade. Notably, the Cladocopium C1 sub-clade has a high relative abundance in clade I, whereas the heat-tolerant Cladocopium C40 and C3u sub-clades subdominante in clade II. Regarding bacterial communities, Cycloseris costulata , the earliest divergent species, had higher bacterial β-diversity, while the latest divergent species, Lithophyllon scabra , displayed lower bacterial α-diversity and higher community stability. Beneficial bacteria dominante Fungiidae’s bacterial community (54%). The co-occurrence network revealed that microbial networks in clade II exhibited lower complexity and greater resilience than those in clade I. Our study highlights that host evolutionary radiation and microbial communities shaped Fungiidae’s thermal tolerance. The variability in subdominant Symbiodiniaceae populations may contribute to interspecific differences in thermal tolerance along the evolutionary branches of Fungiidae. The presence of abundant beneficial bacteria may further enhance the thermal ability of the Fungiidae. Furthermore, the later divergent species of Fungiidae have stronger heat tolerance, possibly driven by the increased regulation ability of the host on the bacterial community, greater microbial community stability, and interaction network resistance. IMPORTANCE Coral reefs are facing significant threats due to global warming. The heat tolerance of coral holobionts depends on both the coral host and its microbiome. However, the association between coral evolutionary radiation and interspecific differences in microbial communities remains unclear. In this study, we investigated the role of evolutionary radiation and microbial community dynamics in shaping the thermal acclimation potential of Fungiidae in the Sanjiao Reef of the southern South China Sea. The study’s results suggest that evolutionary radiation enhances the thermal tolerance of Fungiidae. Fungiidae species that have diverged more recently have exhibited a higher presence of heat-tolerant Symbiodiniaceae taxa, more stable bacterial communities, and a robust and resilient microbial interaction network, improving the thermal adaptability of Fungiidae. In summary, this study provides new insights into the thermal adaptation patterns of corals under global warming conditions.

Funder

MOST | National Natural Science Foundation of China

Self-Topic Project of Guangxi Laboratory on the Study of Coral Reefs in the South China Sea

Central Public-interest Scientific Institution Basal Research Fund

Publisher

American Society for Microbiology

Reference153 articles.

1. Diversity in Tropical Rain Forests and Coral Reefs

2. R Ea Ka-Kudla ML. 1997. The global biodiversity of coral reefs: a comparison with rainforests. Biodiversity Understanding & Protecting Our Biological Resources.

3. Changes in the global value of ecosystem services

4. A global analysis of coral bleaching over the past two decades

5. Shelters and Their Use by Fishes on Fringing Coral Reefs

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