Overexposure to ultraviolet radiation (UVR) emitted by the sun can damage and kill living cells in animals, plants, and microorganisms. In aquatic environments, UVR can penetrate nearly 47 m into the water column, severely impacting many marine organisms. Jellyfish are often considered resilient to environmental stressors, potentially explaining their success in environmentally disturbed areas, but the extent of their resilience to UVR is not well known. Here, we tested resiliency to UVR by exposing benthic polyps of the moon jellyfish, Aurelia sp., to UVA and UVB—the two types of UVR that reach Earth’s surface—both separately and in combination. We quantified asexual reproduction rates and polyp attachment to hard substrate, in addition to qualitative observations of polyp health. There were no differences in asexual reproduction rates between polyps exposed to isolated UVA and polyps that received no UVR. Polyps reproduced when exposed to short term (∼7–9 days) isolated UVB, but long-term exposure limited reproduction and polyp attachment to the substrate. When exposed to both UVA and UVB, polyps were unable to feed and unable to remain attached to the substrate, did not reproduce, and ultimately, experienced 100% mortality within 20 days. Although many studies only examine the effects of UVB, the combination of UVA and UVB here resulted in greater negative impacts than either form of UVR in isolation. Therefore, studies that only examine effects of UVB potentially underestimate environmentally relevant effects of UVR. These results suggest that polyps are unsuccessful under UVR stress, so the planula larval stage must settle in low-UVR environments to establish the success of the polyp stage.
Microbiomes play an essential role in promoting host health and fitness, but the factors affecting variation in gut microbiomes among individuals are not fully understood. Investigating the microbiome under different conditions is needed to link gut microbiomes to host physiology and potentially design manipulations to improve rearing success of captive species. In this study, we characterized the gut microbiomes of Atlantic salmon (Salmo salar) in individuals at different life stages, vaccination status, and hatchery origin. Microbiomes differed between age-0 sub-adults and adults, with sub-adults exhibiting higher diversity and more similar communities when compared to adults. We also found that vaccines against bacterial kidney disease reduced gut microbial diversity within individual sub-adult salmon, resulting in dissimilar gut microbial communities among individuals. The diversity and structure of microbiomes did not differ between groups of adults that were reared in two different hatcheries and sampled from the wild. Sub-adults, particularly unvaccinated sub-adults, displayed a strong core microbiome present in the majority of individuals. Our results suggest that life stage and vaccination status are essential factors in the gut microbiome development of salmon. Conditions experienced during early life stages appear to have a strong influence on the microbiome, but differences among individuals at early life stages may be lost due to environmental factors experienced later in life. The plasticity of the microbiome throughout the life of individuals may have important implications for understanding host health, with potential applications for improving the rearing and reintroduction success of the ecologically and economically important Atlantic salmon.
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