Abstract
Korean Saccharina japonica is highly valued, both for human consumption and abalone feed. For the stable production of abalone feed, fresh seaweed biomass is required throughout the year. However, currently, the production of farmed Saccharina is limited by environmental conditions such as temperature, irradiance, and nutrient availability between August and November. Due to shortages experienced in supply, the production of early-season biomass can be highly profitable and, therefore, some famers attempt to start their cultivation activities before prevailing, surface seawater temperatures (SST) are optimal. However, attempting to cultivate too early, can lead to total crop failure. Young kelp sporophytes are easily destroyed between 18 and 22 °C SST, which can occur during the early nursery period when the materials are confined to tanks. This study investigated the growth of S. japonica thalli and photosynthetic quantum yield (Fv/Fm) under five temperatures (i.e., 18–26 °C, at 2° increments) and five irradiances (i.e., 5, 10, 20, 40, and 80 μmol photons m−2 s−1). This was undertaken for four different size groups of sporophyte thalli (i.e., 0.25, 1, 5, 10 mm). There were different responses of the initial groups of S. japonica showing different tolerances to temperature and irradiance. In general, the smaller plants (1 mm) were more tolerant of sub-optimal conditions than their larger cohorts. These results indicated the optimum temperature and irradiance ranges for different size groups of S. japonica thalli which, if adopted in management protocols, could contribute to enhanced profitability and a more stable and evenly distributed production of Saccharina raw materials over an entire annual basis.






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References
Adey WH, Steneck RS (2001) Thermogeography over time creates biogeographic regions: a temperature/space/time integrated model and an abundance-weighted test for benthic marine algae. J Phycol 37:677–698
Andersen GS, Pedersen MF, Nielsen SL (2013) Temperature acclimation and heat tolerance of photosynthesis in Norwegian Saccharina latissima (Laminariales, Phaeophyceae). J Phycol 49:689–700
Boderskov T, Schmedes PS, Bruhn A, Rasmussen MB, Nielsen MM, Pedersen MF (2016) The effect of light and nutrient availability on growth, nitrogen, and pigment contents of Saccharina latissima (Phaeophyceae) growth in outdoor tanks, under natural variation of sunlight and temperature, during autumn and early winter in Denmark. J Appl Phycol 28:1153–1165
Davison IF (1991) Environmental effects on algal photosynthesis: temperature. J Phycol 27:2–8
van den Hoek C, Lüning K (1988) Biogeography of marine benthic algae – preface. Helgoländer Meeresunters 42:131–132
van den Hoek C, Breeman AM, Stam WT (1990) The geographic distribution of seaweed species in relation to temperature—present and past. In: Beukema JJ, Wolff WJ, Brouns JJW (eds) Expected effects of climatic change on marine coastal ecosystems. Kluwer Academic, Dordrecht, pp 55–67
Diez I, Muguerza N, Santolaria A, Ganzedo U, Gorostiaga JM (2012) Seaweed assemblage changes in the eastern Cantabrian Sea and their potential relationship to climate change. Estuar Coast Shelf Sci 99:108–120
Harley CDG, Anderson KM, Demes KW, Jorve JP, Lordas RL, Coyle TA, Graham MH (2012) Effects of climate change on global seaweed communities. J Phycol 48:1064–1078
Liu F, Sun X, Wang F, Wang W, Liang Z, Lin Z, Dong Z (2014) Breeding, economic traits evaluation, and commercial cultivation of a new Saccharina variety “Huangguan no. 1”. Aquacult Int 22:1665–1675
Lobban CS, Harrison PJ, Duncan MJ (1985) The physiological ecology of seaweeds. Cambridge Univ Press. Cambridge, 242p
Lüning K (1980) Critical levels of light and temperature regulating the gametogenesis of three Laminaria species (Phaeophyceae). J Phycol 16:1–15
Lüning K (1984) Temperature tolerance and biogeography of seaweeds: the marine algal flora of Helgoland (North Sea) as an example. Helgoländer Meeresunters 38:305–317
MOF (2015) Statistical data of the Ministry of Oceans and Fisheries. https://www.fips.go.kr Cited 25 Mar 2016
Müller R, Laepple T, Bartsch I, Wiencke C (2009) Impact of oceanic warming on the distribution of seaweeds in polar and cold-temperate waters. Bot Mar 52:617–638
Nielsen MM, Kumar JP, Soler-Vila A, Johnson MP, Bruhn A (2016) Early stage growth responses of Saccharina latissima spores and gametophytes. Part 1: inclusion of different phosphorus regimes. J Appl Phycol 28:387–393
Parry ML, Canziani OF, Palutikof JP, van der Linden PJ, Hanson CE (2007) Climate change 2007: impacts adaptation and vulnerability. Contribution of Working Group II to the fourth assessment report of the Intergovernmental Panel on Climate Change IPCC Fourth Assessment Report (AR4), Vol 2, IPCC, Cambridge, pp 976
Qian R, Zhang ZHZ, Li XJ, Pan JH, Sheng BL, Jiang YX (2016) Guidelines on disease prevention and treatment during seedling period of kelp. China Fisheries 6:96–99 (in Chinese)
Salvucci ES, Crafts-Brandner SJ (2004) Relationship between the heat tolerance of photosynthesis and the thermal stability of Rubisco activase in plants from contrasting thermal environments. Plant Physiol 134:1460–1470
Schreiber U, Schliwa U, Bilger W (1986) Continuous recording of photochemical and non-photochemical chlorophyll fluorescence quenching with a new type of modulation fluorometer. Photosynth Res 10:51–62
Serisawa Y, Yokohama Y, Aruga Y, Tanaka J (2002) Growth of Ecklonia cava (Laminariales, Phaeophyta) sporophytes transplanted to a locality with different temperature conditions. Phycol Res 50:201–207
Shan TF, Liu F, Liu QS, Pang JS (2011) An overview of the “summer sporeling” technique of Saccharina japonica in China. J Agricultural Sci Technol 13:129–134 (in Chinese with English abstract)
Su L, Pang SJ, Shan TF, Li X (2017) Large-scale hatchery of the kelp Saccharina japonica: a case study experience at Lvshun in northern China. J Appl Phycol 29:3003–3013
tom Dieck I (1993) Temperature tolerance and survival in darkness of kelp gametophytes (Laminariales, Phaeophyta): ecological and biogeographical implications. Mar Ecol Prog Ser 100:253–254
Tseng CK (1981) Commercial cultivation. In: Lobban CS, Wynne MJ (eds) The biology of seaweeds. Blackwell Scientific Publications, Oxford, pp.680–725
Wahid A, Gelani S, Ashraf M, Foolad MR (2007) Heat tolerance in plants: an overview. Env Exp Bot 61:199–223
Wernberg T, Thomsen MS, Tuya F, Kendrick GA, Staehr PA, Toohey BD (2010) Decreasing resilience of kelp beds along a latitudinal temperature gradient: potential implications for a warmer future. Ecol Lett 13:685–694
Wernberg T, Russell BD, Thomsen MS, Gurgel CFD, Bradshaw CJ, Poloczanska ES, Connell SD (2011) Seaweed communities in retreat from ocean warming. Curr Biol 21:1828–1832
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This work was supported by a grant from the National Institute of Fisheries Science (R2018011).
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Hwang, E.K., Ha, D.S. & Park, C.S. The influences of temperature and irradiance on thallus length of Saccharina japonica (Phaeophyta) during the early stages of cultivation. J Appl Phycol 30, 2875–2882 (2018). https://doi.org/10.1007/s10811-018-1565-4
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DOI: https://doi.org/10.1007/s10811-018-1565-4


