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The optimal water temperature in seed germination and the upper critical water temperature in seedling growth were determined for Zostera japonica collected from Ago Bay, Japan. The relationship between the seed germination rates and seed storage period (0, 30, and 60 days) at 0°C was also examined. The optimal water temperature in seed germination was in the range 15-20°C regardless of the storage period, in which germination rates were up to 14%. Seedlings, grown from seeds up to 10 cm in total length, were cultured for 1 week at various water temperatures to measure their relative growth rates. The optimal water temperature in early growth was in the range 20-25°C; relative growth rates ranged from 3.8 to 4.2%. Seedlings could survive up to a water temperature of 29°C, but most seedlings withered at 30 or 35°C.The optimal water temperatures for seed germination and seedling growth were related to the seasonal changes of water temperature in the sampling site. Although seedlings were hardly observed in Ago Bay in summer, Z. japonica might extend its distribution as far as where the summer water temperature is lower than 29°C.

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Photosynthesis and respiration rates were measured on 10 cm tall seedlings of Z. japonica at various temperatures and photosynthetic photon flux densities (PPFDs), and the daily compensation points in each season were estimated with a mathematical model based on photosynthetic properties and diurnal changes in solar irradiances. The seedlings were grown from seeds collected at Tategami-ura, Ago Bay, Mie Prefecture, Japan, and cultured for 1 week under the examined temperatures of 10-25°C. The estimated daily compensation points of Z. japonica ranged from 9.3 to 13.6% of the surface irradiance. The total PPFDs in daytime ranged from 3.8 to 5.3 mol photons m -2 day -1 . The theoretical depth limits were calculated by the Beer-Lambert law concerning the relative light intensities of the sea surface and the extinction coefficient. The estimated lowest limit of Z. japonica agreed well with the lowest depth (7 m) previously reported. Therefore, the mathematical model in this study can be used to estimate the production and critical growing depth of Z. japonica. Differences in light requirements seem to be one of the reasons for the shallower habitats of Z. japonica in comparison with Z. marina.

This study was designed to identify a sustainable Zostera marina population based on the relationships between the distributional patterns of shoots and light conditions in the population. Population structures and light conditions on 22 April 2003 (season of reducing shoot density), 27 September 2003 (season of the annual minimum density and biomass) and 9 April 2004 (season of the annual maximum density and biomass) were examined. On 22 April 2003, the frequency distribution in shoot length was almost even. The spatial pattern is characterized by small clumps within 2-5 cm radius. On 27 September 2003, the lengths of all shoots were less than 40 cm, and the distributional patterns were similar to 22 April. On 9 April 2004, the spatial pattern is characterized by larger clumps within 25 cm radius. The reproductive shoots had a regular distribution. The relative light intensities on the population floor of the sea surface on 27 September and 9 April were 53.3 and 10.2%, respectively. The light intensity on 9 April 2004 was not sufficient for growth. The results suggest that the competition for harvesting solar radiation is caused by the shoot length and the spatial pattern among shoots in the population.