The effect of the water-soluble UV-absorbing substance (UVAS) extracted from the marine red alga Porphyra yezoensis Ueda on UV-dependent thymine photodimer production was investigated. The T<>T pyrimidine-pyrimidone 6-4 dimer and the cyclobutane cis-syn T<>T 5-6 dimer produced by UV irradiation with a xenon lamp were analyzed by reverse-phase high-performance liquid chromatography. Although the dimer production was reduced when the irradiation was filtered through a UVAS solution, it decreased more when thymine was mixed with UVAS. Furthermore, UVAS inhibited the degradation of UV-irradiated thymine. The inhibitory effect of UVAS was significantly greater than that of exogenously added adenine or guanine, which forms complementary base pairs with thymine. These data suggest that in addition to its filtering effect against UV radiation, UVAS also protects thymine by a direct molecule-to-molecule energy transfer process. The protective function of UVAS against UV irradiation is advantageous for this alga under strong UV irradiation.

Gametophytes of two Undaria species, U. pinnatifida and U. undarioides (Laminariales, Phaeophyceae), were studied to determine their water temperature requirements in order to understand their different distributions in Mie Prefecture, Japan. The optimal temperature for growth was 20 ° C for gametophytes of both species, and the upper critical temperature for growth was also the same for both species at 28 ° C. Therefore, the optimal and critical temperatures for growth of the gametophytes are not the main factors determining distribution. The optimal temperature for maturation of U. pinnatifida was approximately 10-15 ° C, whereas it was closer to 20-21 ° C for U. undarioides , a difference between these species of at least 5 ° C. In autumn and early winter, the seawater temperature at the mouth of Ise Bay, where U. pinnatifida is distributed, ranges from 21.6 ° C (October) to 12.7 ° C (December), and off Hamajima, where U. undarioides is found, the range is from 22.7 ° C (October) to 19.1 ° C (December). The seawater temperatures from October to December, which is the maturation season for the gametophytes, agreed well with the optimal temperature requirements for maturation of the gametophytes of both species. Thus the difference in the maturation temperature range of the gametophytes is a major factor determining distribution of these Undaria species along the Japanese coast.

SUMMARY: The productive structure and productivity of a Sargassum macrocarpum C. Agardh population were studied from June 1993 to July 1994 in Fukawa Bay facing the Sea of Japan, Yamaguchi Prefecture. S. macrocarpum formed a dense population at a depth of 8 m in the study area. Using the stratified clip technique, monthly changes in the productive structure from 1993 to 1994 were clarified. The dry weight of leaves and main branches increased with the elongation of branches. Thalli in the middle to high stratum began to bear receptacles from March 1994 and the dry weight of receptacles was approximately one‐third of the standing crop in June. The loss of leaves increased from April to June 1994, and the loss of main branches and receptacles from June to July 1994. Productivity of branches and receptacles reached maxima of 4.67 g dry wt/m2 per day from February to March and 5.33 g dry wt/m2 per day from April to May, respectively. Productivity of the leaves, however, was almost constant at approximately 2 g dry wt/m2 per day from July 1993 to March 1994. Therefore, maximum productivity of the S. macrocarpum population of 7.17 g dry wt/m2 per day occurred from February to March. Annual net production of newly sprouting branches in June 1993 was 1600.1 g dry wt/m2 per year based on the summation method, which was calculated from the monthly changes in the productive structure.

The optimal water temperature in seed germination and the upper critical water temperature in seedling growth were determined for Zostera marina collected from Ise 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 for seed germination was in the range from 10 to 15°C regardless of the storage periods, in which germination rates ranged from 35 to 57%. Seedlings grown from seed up to 10 cm in total length were cultured for 1 week under various water temperatures to measure their relative growth rates. The optimal water temperature in growth was in the range from 20 to 25°C; relative growth rates ranged from 2.0 to 2.6%. Seedlings could survive up to a water temperature of 28°C, but most seedlings withered at 29 or 30°C. The optimal water temperatures for seed germination and seedling growth were related to the seasonal changes of water temperature at the sampling site. Although seedlings were rarely observed in the field in summer, they can grow at temperatures as high as 28°C. Therefore, Z. marina may extend its distribution as far as where the summer water temperature is lower than 28°C.

The present study was designed to estimate the critical light intensity required for growth of Zostera marina and that which determines its depth limit. Seeds of Z. marina collected at Matsunase, Ise Bay, Mie Prefecture, central Japan were germinated and grown to young plants of 10 cm in length. The young Z. marina were cultured for 1 week in various water temperatures, and their photosynthesis and respiration were measured under various photon irradiances. The daily compensation point was estimated by a mathematical model based on photosynthetic activity and diurnal changes in solar irradiance. The estimated daily compensation point of young Z. marina was 5.7% of sea surface. The depth limit was determined by the Beer–Lambert law concerning the relative solar irradiance on the sea surface and the extinction coefficient. Almost all previous studies report a shallower growing depth of Z. marina than the present result, but the lowest reported data agreed well with the current estimated depth limit. Therefore, the mathematical model in the present study can estimate the production and critical growing depth of Z. marina. The results suggest that the compensation depth is controlled mainly by the solar irradiance reaching the Z. marina beds.