Miyuki Maegawa

UV-Absorbing Substance in the Red Alga Porphyra yezoensis (Bangiales, Rhodophyta) Block Thymine Photodimer Production

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.

Temperature requirements for seed germination and seedling growth of Zostera marina from central Japan

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.

Temperature requirements for the growth and maturation of the gametophytes of Undaria pinnatifida and U. undarioides (Laminariales, Phaeophyceae)

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.

Critical light conditions for young Ecklonia cava and Eisenia bicyclis with reference to photosynthesis

The brown algae Ecklonia cava and Eisenia bicyclis are widely distributed along the Pacific coast of central Japan, and are important algae both ecologically and economically. Wherever the water condition and substratum are suitable, these species form a dense marine forest in the sublittoral zone. Considerable knowledge has been accumulated on their distribution and population structure from the ecological point of view (Hayashida, 1977; Iwahashi, 1968; Iwahashi et al., 1979; Kida & Maegawa, 1982, 1983, 1985; Ohno & Ishikawa, 1982; Taniguchi & Kato, 1984; Maegawa & Kida, 1984a, b). There are, however, few studies of their photosynthesis, knowledge of which is important for estimating the primary production (Y. Sakanishi, Y. Yokohama & Y. Aruga, unpubl.).

Temperature requirements for the growth of young sporophytes of Undaria pinnatifida and Undaria undarioides (Laminariales, Phaeophyceae)

The relative growth rate of young sporophytes of Undaria pinnatifida (Harvey) Suringar and Undaria undarioides (Yendo) Okamura was examined in order to understand the difference in distribution of these two species around the coast of Japan. The optimal temperature for growth of both species was similar at 20°C and the upper critical temperature for growth was also similar, at 27°C for U. pinnatifida and 26°C for U. undarioides. Therefore, the optimal and upper critical temperatures for growth of the young sporophytes are not the main factors determining the distribution of each species. Next, the lower critical temperatures for growth were examined. For the young sporophytes of U. pinnatifida, the lower limit was less than 5°C while for those of U. undarioides it was 15°C. Thus, the difference in the lower critical temperature for growth between the two species was approximately 10°C. During the period of young sporophyte growth in the field, the temperature at the mouth of Ise Bay, Japan, where U. pinnatifida occurs, ranges from 12.7°C in December to 13.1°C in April, with a minimum of 7.9°C in February. Our experiments indicate that young sporophytes are able to grow throughout this period. The temperature off Hamajima, Japan, where U. undarioides occurs, ranges from 19.1°C to 14.8°C during the same time period. Again, young sporophytes are able to growth throughout this period, although minimum winter temperatures are only just high enough for growth. These natural temperature ranges during the growth season of the sporophytes agree well with the experimentally determined temperature requirements for growth of each species. Therefore, the difference between the two species in the critical temperature required for growth of the young sporophytes, especially in the low temperature range, is one of the major factors determining the distribution pattern of each species.

Effect of seasonal changes in the photosynthates mannitol and laminaran on maturation of Ecklonia cava (Phaeophyceae, Laminariales) in Nishiki Bay, central Japan

Seasonal changes in the contents of two photosynthates, namely, mannitol and laminaran, were investigated in Ecklonia cava Kjellman with reference to its maturation. The samples were collected from a depth of 8 m in Nishiki Bay, central Japan. The mannitol and laminaran contents in the bladelets were measured. We also determined the content of these photosynthates in the bladelets occupying different positions on the frond and in the sorus and non‐sorus portions of the bladelets. The maturation of sori initiated in July and peaked in October. The content of the two photosynthates in the bladelets was low in winter; this coincided with the active formation of new bladelets. Mannitol levels were high during the beginning of the maturation season in summer. Laminaran, in particular, was present in the bladelets only in summer. The laminaran content was higher in the sorus portions than in the non‐sorus ones; however, the mannitol content was almost equal in both portions. The laminaran content was high only in the bladelets just prior to maturation and in the mature bladelets at the beginning of the maturation season. These results suggested that mannitol and laminaran were important energy sources for the maturation of E. cava from summer to autumn, and laminaran in particular was closely associated with the maturation of reproductive structures.

High water-temperature tolerance in photosynthetic activity of Zostera marina seedlings from Ise Bay, Mie Prefecture, central Japan

Photosynthetic activities of seedlings of Zostera marina were successively measured using a gas volumeter for 6 days at seven light (0–400 μmol photons/m2 per s) and 11 water temperature conditions (5–35°C). The seedlings were collected from mature plants (Ise Bay, central Japan), and stored and cultured in incubators accurately controlled at each test temperature. The maximum gross photosynthesis (Pmaxg) was recorded at an optimal water temperature of 29°C after 0 days. After 6 days, Pmaxg appeared at 25°C and most plants cultured at 29–30°C bleached and withered after the drastic increase of light compensation point (Ic). On the contrary, at 5–28°C, the photosynthetic activities either changed little (5–25°C) or recovered after a temporal reduction (26–28°C); seedlings survived and looked healthy after being cultured for 6 days. The recovery was thought to be an acclimation to tolerate higher water temperature. As a result, the critical upper water temperature for Z. marina seedlings was proposed as 28°C. The temperature was consistent with the previously reported maximum water temperature in habitats around the southern boundary of Z. marina in the northern hemisphere.

Effect of laminaran accumulation on maturation in sporophyte fragments from Ecklonia cava (Phaeophyceae, Laminariales) under various laboratory light and temperature conditions

Fragments of Ecklonia cava Kjellman were cultured under controlled laboratory conditions of light irradiance, water temperature, and photoperiod. To clarify the relationship between the maturation of E. cava and the photosynthetic products, laminaran, the content in the fragments was measured with the progress of maturation. The culture conditions ranged from 12.5 to 100 µmol m−2 s−1, 10–25°C, and 14 : 10 h LD (light : dark) to 10 : 14 h LD. In the case of low light conditions, despite an optimum temperature for maturation, the fragments did not form sori and laminaran was not accumulated during the culture period. In the case of sufficient light and non‐optimum temperature conditions, the fragments did not form sori, but laminaran was accumulated. When the fragments were cultured under optimum light and temperature conditions for maturation, laminaran was accumulated in the early stage of maturation, just before or after cortex of the bladelets thickened, and decreased with the progress of maturation, and all fragments matured regardless of the length of the photoperiod. So, these results support the idea that laminaran is used as the main respiratory substrate in the maturation of E. cava.

Rearrangement of the flagellar apparatuses and eyespots of isogametes during the fertilization of the marine green alga, Monostroma nitidum (Ulvophyceae, Chlorophyta)

Behaviors of the flagellar apparatuses (flagella, basal bodies, microtubular roots, etc.), mating structures and eyespots of gametes during the fertilization of Monostroma nitidum were studied using field emission scanning electron microscopy and transmission electron microscopy. The biflagellate isogamete (mt+ and mt−) mating structure has a position that is converse between mt+ and mt− gametes relative to the flagellar beat plane and the eyespot. After the adhesion of mt+ and mt− gametes, gamete fusion occurred between the two mating structures. The cell fusion plane expanded to the cell surface as circumscribed by 1s–2d roots in mt+ gamete and 1d–2s roots in the mt− gamete. Two sets of flagellar apparatuses lay side by side in the planozygote and soon become mutually close. The no. 1 basal body of mt+ gamete and the no. 2 basal body of mt− gamete rotated in a counterclockwise direction, as viewed from the cell anterior. Then, the no. 2 basal body of mt+ gamete and the no. 1 basal body of mt− gamete slid into a face to face position. Finally, four flagella and basal bodies exhibited a cruciate arrangement. The basal bodies of the opposing pair (no. 1 and no. 2) were offset in a counterclockwise orientation by the basal body diameter. The 1s and 2d roots of the mt+ gamete lay nearly parallel to the 1d and 2s roots of the mt− gamete, respectively, at the cell fusion plane. Because of the asymmetric localization of the mating structure, association, and subsequent rearrangement of basal bodies and microtubular roots, two eyespots lay on the same side of the planozygote. After the settlement of the planozygote, the flagellar apparatus started to disintegrate in the zygote cytoplasm.

Relationship between distribution patterns of shoots and light conditions on population floor in Zostera marina population

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.