ALBERT

Description: Background: Kelps (Laminariales, Phaeophyceae) are brown macroalgae of utmost ecological, and increasingly economic, importance on temperate to polar rocky shores. Omics approaches in brown algae are still scarce and knowledge of their acclimation mechanisms to the changing conditions experienced in coastal environments can benefit from the application of RNA-sequencing. Despite evidence of ecotypic differentiation, transcriptomic responses from distinct geographical locations have, to our knowledge, never been studied in the sugar kelp Saccharina latissima so far. Results: In this study we investigated gene expression responses using RNA-sequencing of S. latissima from environments with contrasting temperature and salinity conditions – Roscoff, in temperate eastern Atlantic, and Spitsbergen in the Arctic. Juvenile sporophytes derived from uniparental stock cultures from both locations were pre-cultivated at 8 °C and SA 30. Sporophytes acclimated to 0 °C, 8 °C and 15 °C were exposed to a low salinity treatment (SA 20) for 24 h. Hyposalinity had a greater impact at the transcriptomic level than the temperature alone, and its effects were modulated by temperature. Namely, photosynthesis and pigment synthesis were extensively repressed by low salinity at low temperatures. Although some responses were shared among sporophytes from the different sites, marked differences were revealed by principal component analysis, differential expression and GO enrichment. The interaction between low temperature and low salinity drove the largest changes in gene expression in sporophytes from Roscoff while specimens from Spitsbergen required more metabolic adjustment at higher temperatures. Moreover, genes related to cell wall adjustment were differentially expressed between Spitsbergen and Roscoff control samples. Conclusions: Our study reveals interactive effects of temperature and salinity on transcriptomic profiles in S. latissima. Moreover, our data suggest that under identical culture conditions sporophytes from different locations diverge in their transcriptomic responses. This is probably connected to variations in temperature and salinity in their respective environment of origin. The current transcriptomic results support the plastic response pattern in sugar kelp which is a species with several reported ecotypes. Our data provide the baseline for a better understanding of the underlying processes of physiological plasticity and may help in the future to identify strains adapted to specific environments and its genetic control.

Description: Spores represent the most vulnerable life history stage of kelps. While UV-induced inhibition of spore germination has been readily documented, the impact of in situ underwater radiation below kelp canopies has been largely overlooked. We determined spectral composition and intensity of underwater radiation along a density gradient in an Alaria esculenta kelp forest at 3 m depth in Kongsfjorden, Svalbard. Accordingly, we set up a laboratory experiment simulating five different radiation conditions corresponding to irradiances under very dense to no canopy cover on a cloudless summer day. Spore responses (photosynthetic quantum yield, pigment and phlorotannin contents, swimming activity, and germination success) were determined after 4, 8, 16, and 24 h of exposure. In situ spectral radiation composition differed strongly from conditions applied in previous studies, which underestimated photosynthetically active radiation and overestimated UV-radiation effects. Furthermore, spore solutions differed significantly in quantum yield, pigment, and phlorotannin contents upon release. Nevertheless, spores reacted dynamically to different radiation conditions and exposure times. Highest radiation (PAR 61.8 W m−2, 1.9 W m−2 UVA, 0.01 W m−2 UVB) caused photodamage after exposure for ≥ 8 h, while intermediate radiation led to photoinhibition. Lowest radiation (PAR 0.23 W m−2, 0 W m−2 UVA, 0 W m−2 UVB) caused inconsistent reactions. There was a reduction of absolute pigment content in all treatments, but reduction rates of photosynthetic pigments were significantly different between radiation treatments. Soluble phlorotannin content decreased under all conditions but was not significantly affected by experimental conditions. High radiation reduced swimming activity of spores, but experimental conditions had almost no effect on germination success. Consequently, it seems unlikely that in situ radiation conditions negatively affect spores in present and future radiation scenarios.