• Journal of Environmental Science International
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• v.7 no.1
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• pp.8-19
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• 1998

The dicriminant function was introduced to understand the cause and establish the prediction method of red tides occurring In Jinhae Bay. Korea. Two sea re91ons of Masan and Haengam Bays and Dang- dong and Wonmun Bays had different types of causes and patterns for red tides. In Masan and Haengam Bays, the red tides concentrically occurred during June and September. For example, in .lune the red tides occurred from physical and meteorological factors, which are related to the stratification and the increase in planktons. However in August the red tides occurred from the water quality environment, based on these conditoins. Futhermore, in September the red tides were caused by the balance between the meteorological and water quality environmental factors. In contrast to those, In Dangdong and Won-mun Bays, the red tides mainly occurred during July and October and the frequency of occurrence was not as much as Masan and Haengam Bays. Especially, in August and September most meteorological and physical factors or water quality environmental factors appeared to contribute to the occurrence of red tides. This indicates that red tides do not easily occur as they are controlled by various environmental factors particularly in these regions The discriminant functions were applied to predict red tides which they were actually occurred In Masan and Haengam Bays in June. The results showed that they were successful for the prediction of red tide at Haengam Bay but not at Masan Bay. The reason for their discrepancy in Masan Bay could have come from using a slight higher value of pH or COD in May, instead of its value in June.

• Journal of Aquaculture
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• v.6 no.2
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• pp.63-69
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• 1993

Various scales of red tides have frequently occurred in the southern coastal waters of the Korean Penninsula since the late 1970's. Because most shellfish and finfish farms in Korea are located in the southern coastal waters, the impacts of red tides on the aquaculture have been increasing significantly. The Puksin Bay is one of the places where red tides have occurred almost every year since the early 1980's. During $1990\~1991$, mass mortalities of aquacultural species by the red tides were recorded. The causative organisms in this period were Leplocylindrus danicu(November '90 and June '91), Skeletonema costatum(December '90 and August '91), Nitzschia seriata(August '91), and Gymnodinium splendens(July '91). The maximum chlorophyll-a content was $265.7{\mu}g/l$ in the tides. Frequent red tides are associated with the eutropication of the bay. Some relationships between red tides' occurrence and europhication are herein discussed.

• The Korean Journal of Ecology
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• v.18 no.3
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• pp.409-418
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• 1995

As a part of studying the function and structure of the mudflat environment of the Yellow Sea, seawater samples in the overlying waters of sediment near Daesan were collected every hour on March 29 (spring tides) and on April 5 (neap tides), 1995 to study the diurnal distribution of aerobic saprophytic bacteria and their extracellular enzyme activities. The diurnal distribution of aerobic saprophytic bacteria ranged from 1.0 X $10^{2}$ to 7.07 X $10^{3}$ cfu /ml at spring tides and from 1.0 X $10^{2}$ to 8.3 X $10^{3}$ cfu /ml at neap tides. The diurnal variations of aerobic saprophytes at the suface waters were greater than those of middle and bottom waters. However, th diurnal fluctuation of saprophyte numbers at spring tides showed no significant difference compared with that at neap tides. The numbers of three physiological groups of aerobic hacteria (proteolytic, lipolytic and amylolytic bacteria) at the surface waters during spring and neap tides were lower than those at the middles and bottom waters. The diurnal variations of five extracellular enzyme activities at the surface waters during the survey period showed lower values than those at the middle and botton waters. Among the measured extracellular enzyme activities, phosphatase showed the highest. However, the activities of amylase, chitinase and cellulase showed a similar tendency.

• Journal of the Korean earth science society
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• v.30 no.5
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• pp.671-681
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• 2009

In the equilibrium theory of tides by Newton, tide on the Earth is a phenomenon driven by differential gravity contributed both by the Sun and the Moon. Due to the direct link of the generic tidal effect to the oceanic tides, college students in the earth science education department are exposed to this theory through oceanography lectures as well as astronomy lectures. Common oceanography textbooks adopt a non-inertial reference frame fixed to the Earth in which the fictitious, centrifugal force appears. This has a potential risk to provide misconceptions among students in various aspects including the followings: 1) this is how Newton originally derived the equilibrium theory of tides, and 2) the tide is a phenomenon appearing only in rotating systems. We show that in astronomy, a much simpler description, which employs the inertial frame, is generally used to explain tides and thus causes less confusion. We argue that the description used in astronomy is preferable both in the viewpoints of simplicity and ease of interpretation. Moreover, on a historical basis, an inertial frame was adopted by Newton in Principia to explain tides. Thus, the description used in astronomy is consistent with Newton's original approach. We also present various astrophysical tides which do not comply with the concept of centrifugal force in general. We therefore argue that the description used in oceanography should be compensated by that in astronomy, due to its complexity, historical inconsistency and limited applicability.

• Journal of the korean society of oceanography
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• v.31 no.3
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• pp.123-133
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• 1996

We describe here the shallow water tides in the seas around Korea, obtained from a nonlinear barotropic model of tides in a domain encompassing the Yellow Sea, the East China Sea and the East Sea (Sea of Japan). As expected, the shallow water tides are large in the shallow marginal areas around the Yellow Sea, with the M4 tide reaching amplitudes as high as 10 cm near the Korean coast, and quite small in the East Sea. However, we also find that the regions east of the Yangtze River ($126^{\circ}E,$ $30^{\circ}N$) in the East China Sea also sustain large shallow water tides, with $M_{4}$, amplitudes reaching 5 cm. Such large shallow water tides are an important component of altimeter-measured sea levels and should not be ignored in any altimetric analyses of the Yellow Sea and the East China Sea. This study also highlights the desirability of very high resolution models to derive accurate shallow water tides in coastal regions.

• Korean Journal of Environmental Biology
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• v.17 no.3
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• pp.217-232
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• 1999

The author made a special review on/red-tides from the following points: definition, terms, yearly progress of researches, causative organisms, searching the causes, toxins, a loss of lives, damages of aquatic products, reducing aquacultural damages and removal efficiency. Red-tides in Korea were caused by diatoms in the early 1960’s, in the end of 1970’s it was caused by non-toxic dinoflagellates when marine pollutions were growing more and more serious. In the end of 1980’s, red-tides were caused by toxic dinoflagellates. Red-tide was only found in selected areas at first, but recently large-scaled red-tides are frequently found in the southern coastal waters of Korea, causing huge losses of marine life. A plan is greatly needed to reduce the damaging red-tides, and removal systems need to be developed.

• Korean Journal of Remote Sensing
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• v.29 no.3
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• pp.331-335
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• 2013

This study detected red tide areas using the existing Moderate-Resolution Imaging Spectroradiometer(MODIS) and Geostationary Ocean Color Imager(GOCI), and then compared the results between results of two sensors. The coasts of Jeollanam-do in the South Sea of Korea were set as the study area based on the red tide data which occurred on Aug. 26th, 2012. This study compared the results of sensors to detect red tides by using a satellite. In the results of analyzing MODIS by limiting it as chlorophyll concentration and the sea surface temperature which is considered to have red tides by the existing researches, it was possible to delete considerable amount of errors compared to the case of detecting red tides by using only chlorophyll while still there were differences from the range of red tides actually observed. In the results of GOCI by using empirical algorithm for detecting red tides, currently used by Korea Institute of Ocean Science & Technology(KIOST), it was possible to obtain more detailed results than MODIS. However, there was an area misjudged as red tides due to the influence of clouds. Also both MODIS and GOCI extracted red tides were not actually occurring, which might be because they were not able to perfectly distinguish red tides from turbid water in coastal areas with high turbidity.

• Korean Journal of Remote Sensing
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• v.15 no.4
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• pp.321-327
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• 1999

As an example of many possible applications of OSMI data, we present a method to detect red tides. In Korean waters, red tides usually occur in the South Sea where the turbidity is usually high due to strong tidal mixing in the shallow sea. The conventional case 1 chlorophyll algorithm cannot be applied since it cannot distinguish chlorophyll from SS (suspended sediments). In October 1998, a red tide outbreak occurred off the coast of KunSan. We analyzed the SeaWiFS data of the outbreak. The standard SeaWiFS chlorophyll algorithm OC-2 was poor in identifying the red tides. However, comparison of spectra of normalized water-leaving radiance indicates that red tide pixels can be distinguished from sediment-laden pixels. Channel 443 and 555 were effective in showing the spectral characteristics. We suggest K490 algorithm as an example in summarizing the information of the spectra and thereby in distinguishing the red tide pixels. Further development is desirable.

• Journal of Environmental Science International
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• v.9 no.3
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• pp.215-221
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• 2000

The relationship between the distribution of sea surface temperature(SST) and dinoflagellate(Cochlodinium polykrikoides) bloom areas were studied. The SST data were derived from the infrared channels of AVHRR(Advanced Very High Resolution Radiometer) sensor on NOAA(National Oceanic and Atmospheric Administration) 12 and 14 satellites during 1995-1998. The initial water temperature at C. polykrikoides bloom was about 21${\circ}C$ at the coastal areas of the South Sea and along the shore of the East Sea of Korea during the summer season of 1995. The northern limit of red tides was coincident with that of 21${\circ}C$ isothermal line in the East Sea. The red tides that initially bloomed at the coast of Pohang on September 21, 1995 moved to the coast of Uljin on September 26, 1995. The skipped appearance of the red tides in the areas between Pohang and Uljin was due to the East Korean Warm Current, which was moving offshore from Pohang to approach to Uljin. The cold water which was formed by tidal front in the western coast of the South Sea and by upwelling water from deep layer in the southeastern coast of the Korean peninsula played a role in blocking the spreading of red tides during summer season in 1997 and 1998. In conclusion, the distribution of red tides appeared to be dependent on the initial water temperature at red tides bloom. The SST at the red tides varied from 21${\circ}C$ to 25${\circ}C$; 21${\circ}C$, 23${\circ}C$, 24 and 24-25${\circ}C$ in 1995, 1996, 1997 and 1998, respectively.

• ALGAE
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• v.32 no.3
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• pp.199-222
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• 2017

Occurrence of Cochlodinium polykrikoides red tides have resulted in considerable economic losses in the aquaculture industry in many countries, and thus predicting the process of C. polykrikoides red tides is a critical step toward minimizing those losses. Models predicting red tide dynamics define mortality due to predation as one of the most important parameters. To investigate the roles of heterotrophic protists in red tide dynamics in the South Sea of Korea, the abundances of heterotrophic dinoflagellates (HTDs), tintinnid ciliates (TCs), and naked ciliates (NCs) were measured over one- or two-week intervals from May to Nov 2014. In addition, the grazing impacts of dominant heterotrophic protists on each red tide species were estimated by combining field data on red tide species abundances and dominant heterotrophic protist grazers with data obtained from the literature concerning ingestion rates of the grazers on red tide species. The abundances of HTDs, TCs, and NCs over the course of this study were high during or after red tides, with maximum abundances of 82, 49, and $35cells\;mL^{-1}$, respectively. In general, the dominant heterotrophic protists differed when different species caused red tides. The HTDs Polykrikos spp. and NCs were abundant during or after C. polykrikoides red tides. The mean and maximum calculated grazing coefficients of Polykrikos spp. and NCs on populations of co-occurring C. polykrikoides were $1.63d^{-1}$ and $12.92d^{-1}$, respectively. Moreover, during or after red tides dominated by the phototrophic dinoflagellates Prorocentrum donghaiense, Ceratium furca, and Alexandrium fraterculus, which formed serial red tides prior to the occurrence of C. polykrikoides red tides, the HTDs Gyrodinium spp., Polykrikos spp., and Gyrodinium spp., respectively were abundant. The maximum calculated grazing coefficients attributable to dominant heterotrophic protists on co-occurring P. donghaiense, C. furca, and A. fraterculus were 13.12, 4.13, and $2.00d^{-1}$, respectively. Thus, heterotrophic protists may sometimes have considerable potential grazing impacts on populations of these four red tide species in the study area.