Porphyra dentata and P. pseudolinearis, originally described from Japan (Ueda 1932) were recorded in a checklist of marine algae from Korea by Lee and Kang (1986).Porphyra dentata is widely distributed in warm temperate waters (Ueda 1932, Tseng 1948, Tanaka 1952, Kim 1999), whereas P. pseudolinearis is found in cold temperate waters of the North Pacific (Ueda 1932, Tanaka 1952,Kang 1966, Wynne 1972, Scagel et al. 1989, Lindstrom and Cole 1992, 1993, Kim 1999). At present, P. dentata and P.pseudolinearis as the cultivars are crops of the most economical importance to inhabitants along the southern and eastern coast of Korea, respectively and one of the popular Korean marine products. Especially, they are famous for Dolkim (in Korean, meaning of Porphyra growing on the rocky beds in nature). Until now, the cultivated plants are mainly P. tenera and P. yezoensis in Korea (Kim 1999). However, both species are cheaper than the other cultivars (e.g., P. dentata, P. pseudolinearis and P. seriata).Therefore, the cultivation of P. dentata and P. pseudolinearis are very important for the seaweed farmer of Korea.But there are some problems in the farming periods of the both species. The cultivation of P. dentata is limited in higher temperature periods (from September to November),while that of P. pseudolinearis is limited in low-er temperature periods (from December to February). Therefore, seaweed farmers has need for prolongation the farming period of both valuable species in Korea.

Studies on the crossing of Porphyra have been completed in laboratory culture (Suto 1963, Niwa et al. 1993, Shin and Miura 1995, Shin et al. 1996, Shin 1999).

Suto (1963) attempted artificial cross experiments between 5 species including two monoecious (e.g., P. tenera and P. yezoensis) and three dioecious (e.g., P. angusta, P. pseudolinearis and P. umbilicalis). Shin and Miura (1995), Shin et al. (1996) and Shin (1999) succeeded in interspecific crossing between P. tenera and P. yezoensis using their color mutants as genetic markers. Ohme and Miura (1988) and Niwa et al. (1993) reported intraspecific crossing between wild-type and various color mutants of P. yezoensis.

I have been conducting cross experiments between P. dentata and P. pseudolinearis using their field materials as new cultivars for characteristic tests and physiological identification of the hybrid as a part of breeding studies of both species. In present study, the results of interspecific crossing between P. dentata and P. pseudolinearis are reported.

Mature foliose thalli of P. dentata and P. pseudolinearis were collected from the upper intertidal zone at Wando in Chonnam Prefecture, and Pohang in Gyeongbuk prefecture, on 11 and 28 February 1996, respectively (Kim 1999). From these thalli, zygotospores were obtained to start conchocelis cultures. Conchospore liberation in both species was induced by reducing the temperature from 20 to 15°C. The resulting foliose thalli were transferred into round flasks. Cultures were separately conducted by the use of one plant per a flask. The artificial crossing was conducted by using the male thalli of P. pseudolinearis and female thalli of P. dentata. Zygotospores from hybrid were cultured at five temperatures (5, 10, 15, 20, and 25°C) and four photon flux densities (10, 20, 40, and 80 ㎛ol m^-2 s^-1) under photoperiods of 14 L : 10 D and 10 L : 14 D (light : dark). The growth of conchocelis was determined by measuring the diameter of colonies at weekly intervals. Conchospore liberation from matured conchosporangial branches was induced by reducing the temperature from 25 to 15°C. The resulting foliose thalli were cultured at five temperatures (5, 10, 15, 20, and 25°C) and 40 ㎛ol m^-2 s^-1 under photoperiods of 14 L : 10 D and 10 L : 14 D in 300 mL round flask with an air tube. Growth 80was determined from measurements of blade length and width. Modified Grund medium (McLachlan 1973) was used in all cultures and was renewed weekly.

Zygotospores from the hybrid by interspecific crossing between both species were germinated to the conchocelis filaments at 5-25°C (Fig. 1A & B). Conchocelis filaments grew to a colony of about 1.5 mm diameter at 20°C after 3 weeks (Fig. 1C). The conchosporangial branches were produced only from the conchocelis colonies grown at 25°C under both photoperiods (Fig. 1D). Conchospores liberated from the conchosporangial branch were well developed to four cells sporeling (ca. 40 ㎛ long) after 3 days (Fig. 1E & F). Archeospores did not liberate from foliose thalli. Male and female reproductive organs began to occur in the marginal parts of plants, about 10 mm long after 8 weeks at 15°C and 40 ㎛ol m^-2 s^-1 under 14 L : 10 D (Fig. 1G & H). Mature spermatangia had a Hus’s (1902) fomula 64, (a/4, b/4, c/4) or 128, (a/4, b/4, c/8) (Fig. 1G & I). The zygotosporangia contained 8 zygotospores formed by the division pattern (a/2, b/2, c/2) (Fig. 1H & J). The marginal portions of fronds were entire or micro and macroscopic spinulate processes (Fig. 1K & L). The basal portion of frond has the more clear spinulate processes (Fig. 1M). The largest thalli were obtained at 10-20°C under both photoperiods after 18 weeks in culture. These foliose thalli reached to a blade length of about 130 mm under the long photoperiod, and of about 190 mm under the short photoperiod after 14 weeks. The shape of foliose thalli were linear or lanceolate types (Fig. 1N & O). The zygotospores produced either monoecious thalli (Fig. 1P) or dioecious thalli.

The zygotospores of hybrid were germinated into the conchocelis colonies at 5-25°C and four photon flux densities under both photoperiods. Higher growth of conchocelis was observed at 15 and 20°C under both photoperiods (Fig. 2). There were no remarkable differences in the growth of conchocelis according to photon flux densities. The maximum diameter of conchocelis colonies was about 2.5 mm within 10 weeks.

Formation rates of conchosporangial branches at different combinations of temperature and photon flux density are presented in Fig. 3. Conchocelis colonies with conchosporangial branches were produced only at 25°C

and 10-80 ㎛ol m^-2 s^-1 under both photoperiods within 3 weeks. Formation rates of conchosporangial branches reached 100% within 10 weeks. Conchospores did not liberate at any culture conditions.

Liberation of conchospores in hybrid species was obtained by reducing the temperature from 25 to 15°C. Growth of foliose thalli at various temperatures under both photoperiods are shown in Fig. 4. Germlings of the hybrid reached their largest size, about 19 cm long at 20°C under short photoperiod after 14 weeks in cul-

ture, whereas initially thalli grew faster 15°C under long photoperiods. At 5 and 25°C, foliose thalli showed almost no growth. They grew to 10 mm or under in blade length during the culture period. The liberation of spermatia and zygotospores at various temperatures and both photoperiods is presented in Fig. 5. In this hybrid species, archeospores did not liberate in all culture conditions. Their liberation occured at 10 and 20°C under both photoperiods within 11 weeks. The linear or lanceolate shape of fronds, similar to that in nature, was observed under culture conditions that produced rapid growth (Fig. 6).

Hybrid shows a typical biphasic life history of the P. lacerata type (Notoya et al. 1993). Zygotospores mostly developed into conchocelis colonies in all culture conditions. Conchosporangial branches were produced at 25°C only and 10-80 ㎛ol m^-2 s^-1 under both photoperiods. Kim (1999) reported that zygotospores of P. dentata and P. pseudolinearis were germinated into conchocelis colonies and conchosporangial branches were produced at 10-25°C, 10-80 ㎛ol m^-2 s^-1 under short photoperiod. Kim (1999) also reported that formation rates of concho-

sporangia in two species were higher at high temperatures than at low temperatures. This result suggests that the abundance of conchosporangial branches in hybrid were also affected by high temperature (Kurogi and Akiyama 1966). Conchospore liberation in this species was induced by reducing temperature from 25 to 15°C (Kurogi and Akiyama 1966, Iwasaki and Sasaki 1971) and changing photoperiod from 14 L : 10 D to 10 L : 14 D (Kim 1999). In other species for Porphyra such as, P. abbottae and P. perforata (Waaland and Dickson 1983) and P. rosengurtii (Kapraun and Luster 1980) require a photoperiodic change to induce spore liberation (Waaland et al. 1990). Our results agree well with those reported on P. suborbiculata f. latifolia by Iwasaki and Sasaki (1971), on P. columbina by Avila et al. (1986) and on P. spiralis var. amplifolia by Kapraun and Lemus (1987).

Notoya et al. (1993) studied four species of Japanese Porphyra, including P. dentata.They reported that conchosporangial branches were formed at a temperature range of 20 to 25°C, and the fast growth of foliose thalli occured at 20°C in P. dentata. Our results well agree with their results with respect to growth and maturation of both phase which are observed at various temperatures and photon flux densities. P. dentata widely distributed on intertidal zone in the warm, temperate and cold waters (Ueda 1932, Tseng 1948, Kim 1999). Kim (1999) reported that in P. pseudolinearis, the growth of conchocelis and the formation of conchosporangial branches occured at 5-25°C and 10-25°C under all the photon flux densities tested, respectively. Kurogi and Akiyama (1966) and Iwasaki and Sasaki (1971) reported that conchosporangial branches were formed at 15 to 25°C or 27°C in all the species studied.

Kim (1999) reported that the growth of foliose thalli, in P. pseudolinearis and P. dentata was fast at 15°C in early developmental stage. Generally, P. pseudolinearis is distributed in temperate and cold water regions (Tanaka 1952, Kang 1966, Wynne 1972, Perestenko 1982, Scagel et al. 1989, Lindstrom and Cole 1992, 1993).

He also reported that P. pseudolinearis showed almost no growth at 25°C while the blade length of P. dentata did not increase at 5°C for 10 weeks. Our results suggest that hybrid will grow at wide range (10-20°C) temperatures.

The young thallus with denticulate marginal cell rows was observed at 10°C at first, and it was quickly produced at low temperatures than high temperatures. In this study, the monoecious foliose thalli sectored by horizontal line were produced at 10°C and 10 L : 14 D. Hitherto, some authors (Chang and Zheng 1960, Lindstrom and Cole 1992, 1993) reported dioecious Porphyra species with monoecious plants for P. haitanensis, P. lanceolata, P. pseudolanceolata, P. linearis, P. mumfordii, P. lanceolata, P. pseudolinearis and P. purpurea.

P. dentata and P. pseudolinearis are typical dioecious species (Tanaka 1952), but monoecious plants were reported by Hwang (1994) in field and culture observations from Japan and Korea, respectively.

No archeospores were produced under any culture conditions in hybrid species, and neither monospores nor protothalli were produced from the conchocelis phase.

In the anatomical examination of the hybrid, the divisional formulas of spermatangia according to Hus (1902) well agree with those of Tanaka (1952) but zygotosporangia did not.

Based on the results of this study and previous reports of two species in culture (Kurogi and Akiyama 1966, Notoya et al. 1993) and field investigation (Kang 1966, Wynne 1972, Scagel et al. 1989, Lindstrom and Cole 1992), the temperature needed for the growth and maturation of both phases of hybrid falls between low and high temperatures.

In conclusion, these culture studies indicate that the growth and maturation of both the foliose and conchocelis phase of the hybrid are more influenced by temperature than photon irradiance. Furthermore, it is apparent that the hybrid has monoecious and dioecious thalli, and suggests that hybrid more can be eurythermal cultivar than two cultivars, P. dentata and P. pseudolinearis.