• NEWSLETTER 전기공업
• /
• no.97-8 s.177
• /
• pp.19-31
• /
• 1997

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
• /
• v.9 no.1
• /
• pp.40-49
• /
• 2004

An ecological study on a sea urchin population, Strongylocentrotus nudus, a key role species in recovery of macroalgal bed, was conducted in Hosan, Samcheok area on the east coast of Korea. Three experimental plots, namely, AMB (artificially-restored macroalgal bed), BG (barren grounds) and NMB (natural macroalgal bed) were established after a pilot survey in June 2002. Distribution and abundance, grazing rates, predation pressure and predator guilds on S. nudus were estimated in three plots bimonthly from Aug. to Dec., 2002. Abundance of S. nudus was lowest, but median test diameter of the urchin was highest (Kruskal-Wallis test, p-value, p<0.001 in Aug. and p=0.003 in Oct.) in NMB In-situ grazing rate of S. nudus estimated by enclosure cage experiment in NMB was about 12 times higher in Aug. (160.0 mg seaweed/g sea urchin/day) than in Oct. (13.8). Predation intensity measured by tethering experiment was higher in NMB. Most of the predators on S. nudus were invertebrates and no fish predators were found. Predator guilds identified by the fish trap experiment using live or dead sea urchins included who]ks Neptunea arthritica, starfish Asterina pectinifera, hermit crabs Pagurus of. samuelis, Paguristes barbatus, brown shawl crabs Atergatis integerrimus and crabs Actaea subglobosa. High predation pressure on S. nudus in natural macroalgal beds was the likely cause of its low density. Elevated sea urchin density and the consequent lasting deforestation of macroalgae in barren grounds demonstrate the importance of predation pressure on sea urchins.

• ALGAE
• /
• v.19 no.4
• /
• pp.293-301
• /
• 2004

A chain-forming toxic din flagellate, Gymnodinium catenatum (Graham) was known as a paralytic toxin-producer among Gymnodinoid group. In the study, the effects of water temperature, salinity and irradiance on the growth of G. catenatum isolated from Yeosuhae Bay, Korea were investigated. Water temperature range in which G. catenatum showed specific growth rate higher than 0.3 day$^{-1}$ were above about 18${^{\circ}C}$. However, salinity did not have such an effect on growth of G. catenatum. The maximum growth rate (0.5 day$^{-1}$) was obtained at 25${^{\circ}C}$ and 30 psu. The specific growth rate (u) expressed as a polynomial equation as functions of temperature (T; ${^{\circ}C}$) and salinity (S; psu) was $\mu$ = 0.005·T$^2$ - 0.0001164 T$^3$ - 0.063-S + 0.005-S$^2$ - 0.00007608-S$^3$ - 0.003-T-S + 0.00005308-T$^2$-S. Thus, in aspects of water temperature and salinity, the species may be expected to survive in most Korean coastal waters from early summer to autumn. The irradiance-growth curve was described as = 0.16 (I - 10.4)/(1 + 21.8) at 18${^{\circ}C}$ and 30 psu, indicating a half-saturation (Ks) photon flux density (PFD) of 42.6$\mu$mol m$^{-2}s^{-1}$ and compensation PFD (I$_0$) of 10.4$\mu$mol m$^{-2}s^{-1}$. These characteristic responses to irradiance suggest that G. catenatum can reside at the sub-surface.

• Korean Journal of Fisheries and Aquatic Sciences
• /
• v.35 no.5
• /
• pp.490-496
• /
• 2002

In order to detect the DNA heteropolymorphism of chum salmon, selected essential genes were examined in different regional chum salmons, i.e., Korean, Japanese and American by denaturing gradient gel electrophoresis (DGGE) and real time PCR methods. From the promoter regions and introns of growth hormone, mtDNA NDI region, D-loop region, IGF-I, histone H3 and MCH2 several representative primer pairs were obtained and employed for the DGGE with the PCR products from the genomic DNAs of the different regional chum salmons. mtDNA NDI, D-loop region and IGE-I genes showed marked heteropolymorphism between Korean and American chum salmons. Intron C of growth hormone also showed a heteropolymorphism between Korean and Japanese chum salmons. Whereas heteropolnnorphism of histone liH and MCH2 genes was detected among in Korean, Japanese and Asnerican chum salmons in the examined region. The real time PCR disclosed the characteristic incremental production of target DNAs dependent on the heteropolymorphic conditions of genomic DNAa of chum salmons, thus the different regional chum salmons could be grouped by the variable incremental curies. Although the DGGE and real time PCR did not produce the identical results in this study, we suggest that the DGGE and real time PCR could be used for the primary screening of the DNA heteropolymorphism of different animal genome.