Heat‐evolved algal symbionts enhance bleaching tolerance of adult corals without trade‐off against growth

Author:

Chan Wing Yan12ORCID,Meyers Luka1ORCID,Rudd David34,Topa Sanjida H.1,van Oppen Madeleine J. H.12ORCID

Affiliation:

1. School of BioSciences University of Melbourne Parkville Victoria Australia

2. Australian Institute of Marine Science Townsville Queensland Australia

3. Monash Institute of Pharmaceutical Sciences Parkville Victoria Australia

4. Melbourne Centre for Nanofabrication Clayton Victoria Australia

Abstract

AbstractOcean warming has caused coral mass bleaching and mortality worldwide and the persistence of symbiotic reef‐building corals requires rapid acclimation or adaptation. Experimental evolution of the coral's microalgal symbionts followed by their introduction into coral is one potential method to enhance coral thermotolerance. Heat‐evolved microalgal symbionts of the generalist species, Cladocopium proliferum (strain SS8), were exposed to elevated temperature (31°C) for ~10 years, and were introduced into four genotypes of chemically bleached adult fragments of the scleractinian coral, Galaxea fascicularis. Two of the four coral genotypes acquired SS8. The new symbionts persisted for the 5 months of the experiment and enhanced adult coral thermotolerance, compared with corals that were inoculated with the wild‐type C. proliferum strain. Thermotolerance of SS8‐corals was similar to that of coral fragments from the same colony hosting the homologous symbiont, Durusdinium sp., which is naturally heat tolerant. However, SS8‐coral fragments exhibited faster growth and recovered cell density and photochemical efficiency more quickly following chemical bleaching and inoculation under ambient temperature relative to Durusdinium‐corals. Mass spectrometry imaging suggests that algal pigments involved in photobiology and oxidative stress were the greatest contributors to the thermotolerance differences between coral hosting heat‐evolved versus wild‐type C. proliferum. These pigments may have increased photoprotection in the heat‐evolved symbionts. This is the first laboratory study to show that thermotolerance of adult corals (G. fascicularis) can be enhanced via the uptake of exogenously supplied, heat‐evolved symbionts, without a trade‐off against growth under ambient temperature. Importantly, heat‐evolved C. proliferum remained in the corals in moderate abundance 2 years after first inoculation, suggesting long‐term stability of this novel symbiosis and potential long‐term benefits to coral thermotolerance.

Funder

Australian Research Council

Great Barrier Reef Foundation

Paul G. Allen Family Foundation

Publisher

Wiley

Subject

General Environmental Science,Ecology,Environmental Chemistry,Global and Planetary Change

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3