• The Korean Journal of Malacology
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• v.25 no.3
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• pp.189-196
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• 2009

Based on 1,260 samples, the age and growth of purple whelk, Rapana venosa (Valenciennes) (Gastropoda:Muricidae) have been investigated. The samples were collected monthly during one year time (from February, 2004 to January, 2005) from the West Sea of Korea. The age of R. venosa was determined by the ring of the operculum analysis. The relationship between whelk's shell height and ring radius in each ring group was expressed as an equation of linear regression and later a correspondence in each ring formation was determined. Based on the monthly variations in the marginal index (MI) of the operculum, it was assumed that the ring of this species has been formed once a year during the period from July to August. The relationship between shell height and shell width was expressed by the equation SW = 0.7867 SH - 6.3988 ($R^2$=0.8604); and between shell height and total weight by the equation $TW=0.0000626{\times}SH^{3.206}$ ($R^2$=0.8324). The purple whelk's spawning period was estimated through the fatness analysis and has occurred during the period from May to July. Obtained results suggests that the ring formation occurs once a year (in July) and the length of time period since the first ring has been formed on the operculum is approximately 13 months (1.08 year). The purple whelk's growth curves for shell height and total weight fitted to the von Bertalanffy's equation and were expressed as follows: $SH_t=199.653(1-e^{-0.104(t+2.478)}$ $TW_t=1484.105(1-e^{0.104(t+2.478)})^{3.206}$.

• The Korean Journal of Malacology
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• v.12 no.2
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• pp.123-131
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• 1996

진해만 바위해안 조간대에 서식하는 뿔소라과 2종, 대수리(Thais clavigera)와 뿔두드럭고둥(T. luteostoma), 에서 수컷의 성징이 암컷에게서 발현되는 임포섹스 현상을 조사하였다. 임포섹스는 전 조사정점에서 100% 나타나고 있었으므로 본 조사에서 수컷의 성징을 보이지 않은 암컷은 발견할 수 없었다. 임포섹스의 강도를 나타내는 상대 성기 길이 지수(relative penislength index: RPL)는 34.7%에서 81.1%의 범위에 있었다. 특히 마산만 안쪽의 조사정점에서는 암컷의 구성비가 크게 감소하고 어린 개체를 거의 발견할 수 없는 등 개체군이 임포섹스의 영향을 받고 있음을 알 수 있었다. 두 종의 체내에 함유된 트리부틸주석(TBT)과 트리페닐주석(TPT)의 농도를 분석한 결과 각각 0.18-1.45 $\mu\textrm{g}$/g, 0.42-6.30 $\mu\textrm{g}$/g의 범위에 있었으며, 임포섹스의 정도는 트리부틸주석과 트리페닐주석의 체내 농도와 밀접한 관계를 보였다. s 대수리와 뿔두드럭고등의 임포섹스는 우리 나라에서 유기주석 화합물의 오염을 나타내는 좋은 지표로 사용될 수 있으며, TBT의 사용 규제이후 그 효과를 감시하기 위한 용도로도 유용하게 사용될 수 있다.

• Animal cells and systems
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• v.3 no.4
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• pp.375-383
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• 1999

Gonadal development, gametogenesis, reproductive cycle, and first sexual maturity of Reishia clavigera were investigated monthly from July 1998 to June 1999 through cytological and histological observations. R. clavigera had separate sexes, and was an internal fertilizer. The ma1e penis was located near the two tentacles. The ovary and testis were composed of a great number of oogenic lobules and spermatogenic tubules, respectively. The size of ripe oocyte ranged from 130 to 140 ${\mu}$m in diameter. The peripheral cytoplasm of the germinal vesicle of the ripe oocyte in many cases were surrounded by smaller yolk granules, while the eccentric cytoplasm was occupied with larger ones. The reproductive cycle of R. clavigera could be classified into five successive stages: early active, late active, ripe, spawning, and recovery. Spawning of females occurred from early July to August when the seawater reached above 24.8$^{\circ}C$. Spawning of males occurred from early June to August in the water above 22.8$^{\circ}C$. Minimum size for sexual maturity of both sexes was above 10.0 mm in shell height. Each egg capsule was a cylinder or spindle in shape, 4-6 mm in length and 1-2 mm in width. Colors of newly spawned egg capsules showed yellowish white or pale yellow, while those with veliger larvae showed pale black, and released larvae or dead egg capsules showed black violet. The fecundity in an egg capsule ranged from 70 to 91 eggs (mean＝80.28 eggs).

• Korean Journal of Fisheries and Aquatic Sciences
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• v.41 no.4
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• pp.253-260
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• 2008

Gonadal development, gametogenesis, reproductive cycle, spawning, relative weight of flesh, and onset of sexual maturity of the murex shell, Ceratostoma rorifluum, collected from the rocky intertidal zone of Daehang-ri, Buan-gun, Jeollabuk-do, Korea were investigated monthly from January to December 2005 both cytologically and histologically. The gonads were widely placed on the digestive gland located in the posterior spiral fleshy part in the shell. C. rorifluum had separate sexes, and was an internal fertilizer. The sex ratio of females to males was approximately 1:1. The ovary and testis contained a great number of oogenic follicles and spermatogenic tubules, respectively. The oogonia and fully ripe oocytes were $15-19{\mu}m$ and $150-160{\mu}m$ in diameter, respectively, and the cytoplasm of the ripe oocytes contained a number of yolk granules. The relative weight of flesh reached a maximum in August($39.35{\pm}0.40%$), and then decreased rapidly in November($32.75{\pm}1.20%$). The percentages of female and male snails at first sexual maturity with shell heights ranging from 12.1-14.0 mm were 60.0% and 52.9%, respectively, while 100% of the snails of both sexes with shell heights over 18.1 mm were reproductively active. Based on the gonadal development and histological observations, the reproductive cycle of the snail could be categorized into five successive stages: early active(December to May), late active(March to July), ripe(June to September), spawning(July to October), and recovery(October to March). C. rorifluum spawned once a year between July and October, and the majority of spawning occurred in September when the seawater temperature exceeded $23.5^{\circ}C$.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.37 no.5
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• pp.385-392
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• 2004

Gonadal development, gametogenesis, reproductive cycle, gonad index, and flesh weight rate of the murex shell (Ocenebra japonica) collected from the rocky intertidal zone of Buan-gun, Jeollabuk-do, Korea were investigated by means of histological method from January to December 2002. O. japonica had separate sexes, and was oviparous. The gonad was widely situated on the surface of the digestive gland located in the rear of the spiral flesh part in the shell. The male penis was located near the two tentacles. The ovary was composed of a number of oogenic follicles, and the testis was composed of several spermatogenic tubules. The size of ripe oocyte was approximately $140{\mu}m$ in diameter. The gonad index (GI) began to increase in March $(33.24{\pm}2.33)$ and reached the maximum in June $(47.77{\pm}1.90)$ Thereafter, the values decreased from July $(45.12{\pm}3.60)$ to October $(19.32{\pm}2.91)$. The flesh weight rate (FWR) began to increase in January $(25.93{\pm}1.32)$ and reached the maxium in May $(31.78{\pm}1.09)$ Thereafter, the values decreased from June $(31.50{\pm}0.66)$ to October $(24.09{\pm}1.60)$. The reproductive cycle could be classified into five successive stages: early active (October to April), late active (January to June), ripe (May to September), spawning (July to September) and recovery (September to February). The reproductive cycle was closely related to the seawater temperature.

• The Korean Journal of Malacology
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• v.4 no.1
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• pp.1-16
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• 1988

The authors observed histochemical and ultrastructural characters on the osphradium of Rapana venosa Valenciennes using light microscope, scanning and transmission electron microscpes. The results were as follows:1)The basic structure of osphradium was bipectinated shape, which consisted of a septum situating in the center of osphradium and numerous osphradial leaflets. On the other hand, Epidermis of ospradial leaflets formed the structure of pseudostratified ciliated columnar epithelium which was composed of an epithelial cell layer, a basal cel layer and a neuropile. 2) Ciliated dpithelial cells:A large number of these cells were observed on the lateral and ventral regions but a small number of them were observed on the dorsal region. These cells had cylindrical microvilli, slender mitochondria and serve fibers.3) Supporting cells: These cells had cylindrical microvilli, spongy layer, electron dense granules, mitochondria and nerve fibers4) Four types secretory epothelial cells: Four distinct types of secretory epithelial cells were recognized and were arbitrily designated as Type I, Type II, Type III and Type IV.cell type I: These cells contained electron denwe granules(diameter, 0.94-1.56${\mu}{\textrm}{m}$), well developed Golgi apparatus and rough endoplasmic reticula, cell type II: These cills contained two types of granules of the different electron density. One was high electron density granules which were 0.4-1.0${\mu}{\textrm}{m}$ in diameter, The other was low electron density granules which were 0.75-1.2${\mu}{\textrm}{m}$ in diameter.cell type III:These cells had fibrous secretory materials and exhibited strongly positive reaction with Toluidine blue.cell type IV:A large number of this type of cells were observed on the ventral region of ospgradial leaflets and positively reacted with periodic acid Schiff reagent. 5)Dark cells contained several electron dense cillaty rootlets and unmerous granules but cellular organelles were not observed.6) Four types basal cells: Four distinci types of basal cells were recognized and arbitrarily designated as Type I, Type II, Type III and Type IV.Cell type I(light cell): These cells exhibited low electuon density and contained short smooth endoplasmic reticula, several vacuoles and granules.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.9 no.1
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• pp.25-34
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• 1976

The purpose of the present study on the radula of Korean marine gastropods is to determine the systematic position of the species by the radula features. The radula features of 9 Families based on the observation of specimens consisting of 31 species are described briefly as follows. 1. Naticidae; Radula formula 2-1-C-1-2. Rachidian is 3-cusped. All cusps are strong and pointed. The lateral tooth is massive and strong with a huge triangula cusp. Two marginal teethare slender, long and strong. 2. Cymatidae; Radula formula 2-1-c-1-2. Fachidian, 1-cusped. Cusp is strong and acute. The basal margin is toothed with a number of small denticles. The lateral tooth is beak-like and strong with groove inside. The marginal teeth are slender and pointed. 3. Tonnidae; Radula Formula 2-1-C-1-2. Rachidian, 3 cusped. Central cusp is huge, strong and abruptly pointed. Lateral cusp is blunt and relatively small. The lateral tooth and maginal teeth are identical to that of the preceding one. 4. Muricidae; Radula formula 1-C-1. Rachidian has 3 to 5 cusps. Central cusp, long, thick, strong and pointed. Lateral cusps are rather shorter than central, thick, strong and well cut with several minute denticles along outer margin. The lateral tooth is falciform. 5. Pyrenidae; Radula formula 1-c-1 Rachidian lacks of cusp. The base is thin, narrow, small and rectangular. Lateral tooth has 2 cusps with a crescent shaped base. 6. Buccinidae; Radula formula 1-C-1. Rachidian has 3 to 7 cusps. The base is massive and broadened laterally. The lateral tooth is large-and has 2 to 4 cusps. The central cusp is the shortest, and become longer towards the each side. 7. Busyconidae ; Radula formula 1-C-1. Rachidian, 3-cusped with a massive base. All cusps are pointed and strong. Centeral cusp is rather shorter than lateral one. Lateral tooth, 2-cusped. Inner cusp short about one half the length of outer one. 8. Fasciolariidae; Radula formula 1-C-1. Rachidian, 3 to 4-cusped. Very small in size. Lateral tooth broadened laterally with about 10 thin, long, sharp cusps. 9. Volutidae ; Only the rachidian exists. Rachidian, 3-cusped. All cusps are strong and sharply pointed. Central cusp is narrower than lateral ones. Anterior basal margin is concave.