Abstract

The establishment of epibacterial communities is fundamental to seaweed health and fitness, in modulating ecological interactions and may also facilitate adaptation to new environments. Abiotic factors like salinity can determine bacterial abundance, growth and community composition. However, influence of salinity as a driver of epibacterial community composition (until species level) has not been investigated for seaweeds and especially under long time scales. We also do not know how abiotic stressors may influence the ‘core’ bacterial species of seaweeds. Following an initial (immediately after field collection) sampling of epibacterial community of an invasive red seaweed Agarophyton vermicullophylum, we conducted a long term mesocosm experiment for 5 months, to examine the influence of three different salinities (low, medium and high) at two different time points (3 months after start of experiment and 5 months, i.e., at the end of experiment) on the epibacterial community richness and composition of Agarophyton. Metagenomic sequencing showed that epibacterial communities changed significantly according to salinity and time points sampled. Epibacterial richness was significantly different between low and high salinities at both time points. Epibacterial richness also varied significantly between 3 months (after start of experiment) and 5 months (end of experiment) within low, medium and high salinity level. Irrespective of salinity levels and time points sampled 727 taxa consistently appeared in all Agarophyton samples hinting at the presence of core bacterial species on the surface of the alga. Our results indicate that both salinity and time can be major driving forces in structuring epibacterial communities of seaweeds with respect to richness and β-diversity. We highlight the necessity of conducting long term experiments allowing us to detect and understand epibacterial succession over time on seaweeds.

Highlights

  • Salinity can be an overall driver of ecosystem function (Smyth and Elliott, 2016) and is considered as one of the most influential environmental determinants, for distribution of benthic and pelagic organisms (Palmer et al, 2011; Darr et al, 2014) and for microbial community composition (Lozupone and Knight, 2007)

  • There was no significant difference in the epibacterial abundance between the low and medium salinity treatments (GLM negativebinomial, χ21,18 = 27, p = 0.11, Figure 1A), but there was a significant increase in the abundance between T1 and T2 (GLM negativebinomial, χ21,17 = 22, p = 0.02) within these levels

  • We assessed the influence of three different salinities and time on the epibacterial abundance, richness and community composition of an invasive seaweed in a long term mesocosm experiment of 5 months duration

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Summary

Introduction

Salinity can be an overall driver of ecosystem function (Smyth and Elliott, 2016) and is considered as one of the most influential environmental determinants, for distribution of benthic and pelagic organisms (Palmer et al, 2011; Darr et al, 2014) and for microbial community composition (Lozupone and Knight, 2007). Salinity can change community structure and ecological function in Archaea (Xie et al, 2014) and affect bacterial abundance, growth and activity (Caporaso et al, 2011). Salinity fluctuations and their subsequent effect on aquatic organisms are more noticeable in estuaries and brackish water ecosystems as these habitats are characterized by a more or less pronounced salinity gradient (Telesh et al, 2013). Salinity is expected to decrease over the coming decades in the Baltic Sea (BACC Author Team, 2008; BACC II Author Team, 2015) and is considered as a regional climate change induced stressor

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