Convergent photophysiology and prokaryotic assemblage structure in epilithic cyanobacterial tufts and algal turf communities

IF 2.8 3区 生物学 Q1 MARINE & FRESHWATER BIOLOGY
Ethan C. Cissell, Sophie J. McCoy
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引用次数: 0

Abstract

As global change spurs shifts in benthic community composition on coral reefs globally, a better understanding of the defining taxonomic and functional features that differentiate proliferating benthic taxa is needed to predict functional trajectories of reef degradation better. This is especially critical for algal groups, which feature dramatically on changing reefs. Limited attention has been given to characterizing the features that differentiate tufting epilithic cyanobacterial communities from ubiquitous turf algal assemblages. Here, we integrated an in situ assessment of photosynthetic yield with metabarcoding and shotgun metagenomic sequencing to explore photophysiology and prokaryotic assemblage structure within epilithic tufting benthic cyanobacterial communities and epilithic algal turf communities. Significant differences were not detected in the average quantum yield. However, variability in yield was significantly higher in cyanobacterial tufts. Neither prokaryotic assemblage diversity nor structure significantly differed between these functional groups. The sampled cyanobacterial tufts, predominantly built by Okeania sp., were co-dominated by members of the Proteobacteria, Firmicutes, and Bacteroidota, as were turf algal communities. Few detected ASVs were significantly differentially abundant between functional groups and consisted exclusively of taxa belonging to the phyla Proteobacteria and Firmicutes. Assessment of the distribution of recovered cyanobacterial amplicons demonstrated that alongside sample-specific cyanobacterial diversification, the dominant cyanobacterial members were conserved across tufting cyanobacterial and turf algal communities. Overall, these data suggest a convergence in taxonomic identity and mean photosynthetic potential between tufting epilithic cyanobacterial communities and algal turf communities, with numerous implications for consumer-resource dynamics on future reefs and trajectories of reef functional ecology.

附生蓝藻丛和藻类草皮群落中趋同的光生理学和原核生物组合结构。
随着全球变化引发全球珊瑚礁底栖生物群落组成的变化,需要更好地了解区分增殖底栖生物类群的决定性分类学和功能特征,以便更好地预测珊瑚礁退化的功能轨迹。这对于在不断变化的珊瑚礁上具有显著特征的藻类群尤其重要。人们对区分丛生附生蓝藻群落与无处不在的草皮藻群落的特征关注有限。在此,我们将光合产物的原位评估与代谢编码和散弹枪元基因组测序结合起来,以探索丛生底栖蓝藻群落和丛生草皮藻群落的光生理学和原核生物组合结构。在平均量子产量方面未发现显著差异。然而,蓝藻丛的产量变异性明显更高。这些功能组之间的原核生物群落多样性和结构均无明显差异。取样的蓝藻丛主要由 Okeania sp.构建,与草皮藻群落一样,主要由变形菌、固着菌和类杆菌组成。检测到的 ASV 在不同功能群之间的含量差异不大,且完全由属于变形菌门和固着菌门的类群组成。对回收的蓝藻扩增子分布的评估表明,在样本特异性蓝藻多样化的同时,蓝藻的优势成员在簇生蓝藻和草皮藻群落中保持一致。总体而言,这些数据表明丛生附生蓝藻群落和草皮藻群落在分类学特征和平均光合作用潜力方面趋于一致,这对未来珊瑚礁的消费者资源动态和珊瑚礁功能生态学的发展轨迹具有诸多影响。
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来源期刊
Journal of Phycology
Journal of Phycology 生物-海洋与淡水生物学
CiteScore
6.50
自引率
3.40%
发文量
69
审稿时长
2 months
期刊介绍: The Journal of Phycology was founded in 1965 by the Phycological Society of America. All aspects of basic and applied research on algae are included to provide a common medium for the ecologist, physiologist, cell biologist, molecular biologist, morphologist, oceanographer, taxonomist, geneticist, and biochemist. The Journal also welcomes research that emphasizes algal interactions with other organisms and the roles of algae as components of natural ecosystems. All aspects of basic and applied research on algae are included to provide a common medium for the ecologist, physiologist, cell biologist, molecular biologist, morphologist, oceanographer, acquaculturist, systematist, geneticist, and biochemist. The Journal also welcomes research that emphasizes algal interactions with other organisms and the roles of algae as components of natural ecosystems.
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