• Title/Summary/Keyword: excystment

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The Occurrence of a Dinoflagellate Gymnodinium catenatum From Chinhae Bay, Korea

  • KIM Hak Gyoon;MATSUOKA Kazumi;LEE Sam Geun;AN Kyoung Ho
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.29 no.6
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    • pp.837-842
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    • 1996
  • The resting cyst of Gymnodinium catenatum was found in the surface sediments collected from Chinhae Bay in October, 1991. This is the first record of the species in the Korean waters. The relative abundance was low with the maximum of $1.7\%$. The colonial motile form consisting of four cells was observed in 1992 from the excystment of the cyst collected from the Wonmun Bay in Chinhae Bay. No blooms caused by G. catenatum has been observed in Chinhae Bay during the survey.

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Relationship between excystment and abundance of HABs off the southern coast of Korea (남해안연안에서 적조생물 휴면포자 발아와 유영세포 출현과의 관계)

  • 이창규;임월애;정창수;조용철;김학균
    • Proceedings of the Korean Society of Fisheries Technology Conference
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    • 2000.05a
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    • pp.204-205
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    • 2000
  • 최근들어 우리나라 남해안연안은 내만역을 중심으로 편모조류에 의한 적조가 빈번히 발생하고 있는데, 이들 적조는 지역별, 시기별로 일정한 주기성을 보이면서 출현하고 있다. 이러한 적조의 시초는 무엇보다도 적조생물이 형성하는 휴면포자의 발아와 상관성이 있을 것으로 추정된다. 따라서 본 연구에서는 우리나라연안에서 출현하는 주요 적조원인생물 휴면포자의 발아률과 유영세포의 출현량을 조사함으로써 휴면포자의 발아와 유영세포 출현량과의 관련성 여부를 알아보았다. (중략)

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Excretory bladder: the source of cysteine proteases in Paragonimus westermani metacercariae

  • Yang, Hyun-Jong;Chung, Young-Bae;Kang, Shin-Yong;Kong, Yoon;Cho, Seung-Yull
    • Parasites, Hosts and Diseases
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    • v.40 no.2
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    • pp.89-92
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    • 2002
  • The cysteine proteases of Paragonimus westermani metacercariae are involved in metacercarial excystment, host immune modulation, and possibly in tissue penetration. In order to clarify the origin of the enzymes, 28 and 27 kDa cysteine proteases in metacercarial excretory-secretory products were purified through the FPLC system using Mono Q column chromatography. The polyclonal antibodies to the enzymes were produced in BALB/c mice. Immunolocalization studies revealed that both cysteine proteases were distributed at the linings of excretory bladder and excretory concretions of the metacercariae. It was suggested that the excretory epithelium of P. westermani undertake the secretory function of metacercarial cysteine proteases, in addition to its role as a route for eliminating waste products.

Cryptocaryoniasis of cultured flounder, Paralichthys olivaceus in low temperatures (저수온 양식 넙치 Paralichthys olivaceus의 Cryptocaryoniasis)

  • Ji, Bo-Young;Kim, Ki-Hong;Park, Soo-Il
    • Journal of fish pathology
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    • v.10 no.2
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    • pp.97-111
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    • 1997
  • In the winter of 1995, mass mortality occurred in cultured flounder, Paralichthys olivaceus in Gurongpo, Kyoungbuk, Korea. From the observations of moribund and dead fish, parasitic ciliates, which were shown as white spots to the naked eye, were considered to be involved in the mass mortality. From heavily infected flounders, histopathological, morphological and biological characterization of these ciliates were carried out. In the histological observation, many ciliates were found under the epithelia of gill filaments and skin, and caused hyperplasia of epithelial and mucus cells at the infected areas. The ciliates found on the body surface, fins and gills were very similar to Cryptocaryon irritans. However the ciliates showed two different patterns of reproductian, i.e., typical form(palintomy)and atypical form(budding plus multiple fission) at $16^{\circ}C$ of water temperature. The occurrence ratio between typical and atypical form was about 3:2. Tomitogenesis takes 8-14 days in the typical and 13-15 days in the atypical form. In the viability test at different temperatures and salinities, the typical form died below 30‰ at $12^{\circ}C$, below 20‰ at $16^{\circ}C$, below 15‰ at $20^{\circ}C$, and below 25‰ at $24^{\circ}C$, respectively. On the other hand, the atypical form died below 20‰ at $12^{\circ}C$, below 15‰ at 16-$20^{\circ}C$, and below 25‰ at $24^{\circ}C$, respectively. The results suggested that the atypical has better viability at low salinity than that of the typical at low temperatures. In the excystment time and success rates of excystment according to temperatures, the typical form showed 8 days, 30% at $12^{\circ}C$ : 6.5 days, 50%, at $16^{\circ}C$ : 5.5 days, 75% at $20^{\circ}C$ : and 7 days, 10% at $24^{\circ}C$, respectively. On the other hand, the atypical form showed 15.5 days at $12^{\circ}C$ : 14 days, 76.6% at $16^{\circ}C$ : 12 days, 72.2% at $20^{\circ}C$ : 10 days 31.6% at $24^{\circ}C$, respectively. The results suggested that the atypical form had longer excystment time than that of the typical form at any temperature and showed better stability at low temperatures.

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Cyst formation of the marine ciliate, Vorticella sp. using MCCF medium (MCCF 배지를 이용한 해산 섬모충 Vorticella sp.의 cyst형성)

  • JUNG Min-Min;RHO Sum
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.32 no.3
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    • pp.317-319
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    • 1999
  • The ciliate, Vorticella was often observed in the rotifer mass culture tanks as common co-existing organism. This Vorticella performed as a predator for aquatic bacteria population in the rotifer mass culture tanks. This study was carried out to investigate a cyst formation medium of Vorticella in the laboratory for keeping Vorticella seed. The test organism Vorticella sp. was isolated from culture water of rotifer mass culture tanks. The cyst of Vorticella was formed by dried-method for the formation and maintainance of cyst. MCCF (Marine Ciliate Cyst Formation) medium was used for cyst formation (incystment), preservation and return to moving cell (excystment) of the marine ciliate, Vorticella sp. The cyst shape and size were ellipical type and $30.51 \pm1.98\;\mu$m (Avg. $\pm$ SD) of minor axis and $28.89 \pm2.12\;\mu$m (Avg. $\pm$ SD) of minor axis (n=10), The Vorticella cyst was kept in the room temperature ($10\~35^{\circ}C$) and total dark condition (24D:0L) during 1 year. The preserved cyst was transferred to moving cell state (excystment) only by the addition of fresh sea water in the MCCF medium. The five Vorticella sp. moving cells of excysted from cysts showed the growth up to 912$\pm$64 cells/10 ml in MCCF medium during the culture period of 16 days. This MCCF medium was very useful tool for cyst formation and species preservation of marine ciliate Vorticella.

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Life Cycle of Heterotrophic Dinoflagellate Cryptoperidiniopsis brodyi (Dinophyceae) (Cryptoperidiniopsis brodyi (Dinophyceae)의 생활사)

  • Park, Tae-Gyu;Park, Young-Tae;Bae, Heon-Meen
    • Journal of Environmental Science International
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    • v.18 no.1
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    • pp.9-14
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    • 2009
  • Pfiesteriaand Pfiesteria-like organisms were reported to be linked to major fish kills(involving well over a billion fish) in North Carolina and Maryland estuaries on the U.S. east coast during the 1990s. Occurrences of these species have been recently reported from Korean waters including Chinhae Bay and the coast of Yeosu. In this study, the life cycle of Cryptoperidiniopsis brodyi and Pfiesteria piscicida were examined using DAPI staining. Their excystment and growth were stimulated directly by the addition of prey cells such as Rhodiminas salina. Amoeboid stages in C. brodyi and P. piscicida were never observed in culture, even after addition of filter-sterile fish mucus and tissue. The dominant life cycle stages consisted of motile flagellated zoospores and cysts. A typical dinoflagellate life cycle was demonstrated by direct observation and DAPI staining.

A Scanning Electron Microscopic Study of the Glochidial Encystment on the Host Fish (2) (Glochidium larva의 부착으로 인한 숙주어류의 피양형성과정에 관한 주사전자현미경적 연구 (2))

  • Jeong, Kye-Heon;Oh, Young-Sook
    • The Korean Journal of Malacology
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    • v.7 no.1
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    • pp.76-86
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    • 1991
  • A scanning electron microscopic stuey on the glochidial encystment study on the golchidal encystment and excystment of Anodonta fukudai on Acheilognathus yamatsutae, a common natural hostfish, was conducted. The glochidium easily attached to the unscaled surfaces of the host fish such as the fins, lips, and the wall of the buccal cavity. For this study, the fins infected with the glochidia wer mainly observed in a series. The process of encystment was slowly progressed, for 21-25 hours for the early cyst and for 2-4 days for the thick walled cyst. The process of excystmint was visually detected on the 12th day since the attachmint was occurred. The first visible sign was a little tear of the cyst wall covering the hinge and marginal zones of the juvenile clam and once the little sign was appeared the progress of emerging and dettachmint of the juvenile clam from the host was finished relatively in short time. During the process of the encystmint, the cells participationg in covering the attached glochidirm were seened mainly supplied by migration from the surroundings. the shapes of the cells migrating and covering the glochidium were considerably changed and the surface structures of the cells lost their normal pattern of the surface ridges. The unstable forms of the cells were observed almost all throughout the period of the glochidial attachment. No cells of the host epithelium, which were still attached to the juvenile clam energing from the cyst, were observed. The most juvenile clams escaped from the cysts were a little bigger than the glochidia and they were still possessed of the golchidial hooks even though much degenerated. The first growth line was appeared on the shell valves of the juvenild clam when observed right after dettachment.

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Studies on the Glochidial Encystment in Host Fish during the development of Anodonta arcaeformis flavotincta (작은대칭이, Anodonta arcaeformis flavotincta의 유생 발생 중 숙주어류내에서 글로키디움 유생의 피낭 형성과정에 관한 연구)

  • 박갑만
    • Development and Reproduction
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    • v.2 no.1
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    • pp.81-87
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    • 1998
  • A scanning electron microscopic study on the glochidial encystment and excystment during the development of Anodonta arcaeformis flavotincta on Carassius auratus, a common natural host fish, was carried out. The glochidia were attached to the fins, buccal cavity and gills of the host fish within 30 minutes. In this study, the fins of host fish infected with the glochidia were examined in a time series. The attachment rates of the glochidia on the pectoral fins, caudal fin and pelvic fins of the host fish were 30%, 22%, and 17%, respectively. The glochidia which attached to the fish became encysted within 27 hrs. The process of encystment progressed slowly. Ti took 24 to 27 hours in the formation of the primary cyst, and after 5 to 6 days, the larvae was covered completely with the epithelial cels of the host tissues. The process of detachment of juvenile clam was observed on the 8th day after host infection. Most of the juvenile clams have sloughed from the cyst of the host within 15 days. No significant size difference was observed in the glochidia and the juvenile which were found before attachment and after detachment from the cyst of the host fish.

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Effects of Environmental Conditions on Germination of Alexandrium tamarense Cysts from Masan Bay, Korea (마산만에서 분리한 Alexandrium tamarense 휴면시스트의 발아와 환경요인의 영향)

  • 박명환;김영옥;조수연;한명수
    • Korean Journal of Environmental Biology
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    • v.22 no.1
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    • pp.200-205
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    • 2004
  • The effects of environmental eonditions on germination of Alexandrium tamarense cysts were examined. The cysts were isolated from the sediment samples collected from Masan Bay. Germination success was measured by the incubation of cysts under the laboratory conditions and compared in different water temperatures, salinities, and sediment depths. The highest germination rate was recorded at $15^{\circ}C$ and relatively higher germination rate was observed at $10^{\circ}C$ above, while little or no germination occurred at 20 to $25^{\circ}C$. Light and salinity affected little on the excystment. Germination rate according to the sediment depths was higher in the lower layer (5∼10 cm) than in the upper (0∼2 cm) of the sediments collected in March, while higher in the upper than the lower in November. :Based on these results, water temperature seems a principal factor controlling germination of A. tamarense in Masan Bay.