• Animal Systematics, Evolution and Diversity
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• 제24권2호
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• pp.191-197
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• 2008

Specimens of Diophrys appendiculata (Ehrenberg, ] 838) and D. scutum (Dujardin, 1841) have been collected from the coastal and brackish waters around near Ulsan, during 2004-2007. Diophrys appendiculata and D. scutum are described taxonomically for the first time in Korea. Diagnostic characteristics of these species are as follows. Diophrys appendiculata: size in vivo $43-68{\times}25-50{\mu}m$, adoral zone of membranelles (AZM) covering 43-74% of cell length in impregnated and 46-65% in vivo specimens with 32-47 adoral membranelles (AM). Paroral membrane is slightly curved. Four to five dorsal kinetal (DK) rows are fragmented and anterior and posterior parts of rows densely ciliated. Two macronuclear nodules (Ma) irregular and elongated oval in shape and widely separated. D. scutum: size in vivo $125-225{\times}75-140{\mu}m$, AZM extending to the middle of right border of body and covering 50-60% of cell length with 56-75 AMs. Body shape is typically ovoid with prominent concave margin at right posterio-lateral end, and rather thick and wide longitudinal ridge along lower buccal cavity on ventral side. Two macronuclei shaped like a sausage. five to six dorsal kineties.

• Animal cells and systems
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• 제15권3호
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• pp.251-258
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• 2011

Ciliates are considered one of the most diverse protozoa and play significant roles in ecology. For successful taxonomic study of these microscopic eukaryotes, a staining procedure is necessary, due mainly to intrinsic difficulties in recognizing characteristics from living cells. Although molecular taxonomy has been used to resolve the ambiguities associated with traditional morphology-based taxonomy, extraction of genomic DNA from stained ciliate cells is not available yet. In the present study, we describe a method to extract genomic DNA from a single protargol-impregnated euplotid cell. By using $HgCl_2$ as a fixative and modulating the exposure time of bleach solution in the protargol impregnation, high-quality genomic DNA can successfully be extracted from a stained single cell with minimal loss of morphological integrity. This technique will contribute to the effectiveness of combined approaches of molecular and morphological taxonomy from single ciliate cells.

• Animal cells and systems
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• 제12권4호
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• pp.279-286
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• 2008

Development and distribution of larval Dungeness crab, Cancer magister Dana, 1852 were investigated in southeastern Alaska from late May to mid-September in 2004. Larvae were collected during daylight hours at three inner and two outer Glacier Bay stations at the two different depths in the water column, above and below the thermocline. Larval density decreased dramatically for three larval stages, zoeae I(ZI), zoeae IV, and zoeae V(ZV), but relatively little for zoeae II and zoeae III. ZI predominated at all stations in late May and were collected until late July. Larval stages progressed seasonally from ZI to ZV and density decreased from ZI through ZV. The densities of each zoeal stage at the inner and outer bay stations and at the shallow and deep depths were similar. The density of each larval stage above(shallow) and below(deep) the thermocline and between inner and outer bay stations were not significantly different. The occurrence of larval Dungeness crab is dramatically later than in other parts of the species range, in that larvae appear in abundance beginning in late May. The pattern of spatial distribution of larval stages for the inland waters of Alaska was also markedly different than the patterns reported for Dungeness crab larvae from other parts of the species range, in that the early and intermediate stages occurred within inland waters; from British Columbia to California these larval stages increase in abundance with distance offshore.

• Animal cells and systems
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• 제12권4호
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• pp.287-295
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• 2008

Variations of larval abundance and hatch timing of Dungeness crabs, Cancer magister Dana 1852, were investigated. Dungeness crab larvae were monthly collected at 16 stations arrayed in four transects, Upper Chatham, Icy Strait, Cross Sound, and Icy Point, in southeastern Alaska from May to September 1997-2004. Larval abundance at all transects was the highest in June except in the Icy Point transect. Larval abundance was the highest in the Icy Strait transect, moderate in the Upper Chatham and Cross Sound transects, and the lowest in the Icy Point transect. Zoeae I(ZI) was predominated in May; thereafter ZI decreased and late zoeal stages occurred. In May and June, small numbers of late stage larvae unusually co-occurred with ZI in three transects. These late stage larvae may have been transported from where hatching occurs earlier. The timing of ZI occurrence varied interannually and was related to degreedays during the egg incubation period of Dungeness crabs: later larval hatching in 1997 and 2002 when temperatures were colder, while earlier larval hatching in 1998 when temperatures were warmer. The distribution patterns of Dungeness crab larvae in southeastern Alaska were markedly different from those reported from other areas of the species distribution ranges: larvae occurring much later in the year, and late stage larvae occurring in inland waters.

• Animal cells and systems
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• 제3권1호
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• pp.79-87
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• 1999

Mitochondrial DNA (mtDNA) from 54 specimens of the blue mussel (Mytilus edulis) species complex sampled from the southern coast of Korea was assayed for polymorphism with a portion of the COIII gene (336 bp). Fifteen haplotypes were found. PAUP, one-step networks, and PHYLIP analyses revealed the presence of two clearly differentiated mitochondrial clades (termed clades B and E), separated by 3.6% of minimum sequence divergence. The distribution pattern of the species appears to be consistent with category II of the phylogeographic pattern sensu (Avise et al., 1987): the presence of two discontinuous and distinct mtDNA genotypes in the same geographic region. This unusual mitochondrial polymorphism was explained by the presence of the Mediterranean species, M. galloprovincialis, possessing mtDNA of both M. galloprovincialis and M. edulis.

• Animal cells and systems
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• 제14권4호
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• pp.343-349
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• 2010

Ultrastructural studies of vitellogenesis in oocytes and follicle cells during oogenesis in female Protothaca (Notochione) jedoensis were investigated by histological and transmission electron microscope observations. In early vitellogenic oocytes, combined activities of the Golgi complex, mitochondria and rough endoplasmic reticulum in the cytoplasm are associated with autosynthetic vitellogenesis. Furthermore, at this time, many coated vesicles at the basal region of the oolemma of the oocyte lead to the formation of vesicles through endocytosis in the cytoplasm. Through the formation of the coated pits on oolemma during vitellogenesis, the uptake of extrafollicular precursors (nutritive materials) occurs in coated vesicles by endocytosis. Therefore, it is assumed that these exogenous materials are involved in heterosynthetic vitellogenesis. During late oogenesis, exogenous yolk precursors (yolk granules), lipid droplets and proteinaceous yolk granules are present in the cytoplasm of late vitellogenic oocytes. In mature oocytes, small yolk granules appear intermingled and form large mature yolk granules. Thus, two processes of vitellogenesis occur in oocytes by way of endogenous autosynthesis and exogenous heterosynthesis. The follicle cells attached to the oocytes appear to play an integral role in vitellogenesis in this study.

• Animal cells and systems
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• 제16권4호
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• pp.313-320
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• 2012

Genetic variation was surveyed at four microsatellite loci and 1416 base pairs (bp) of the mitochondrial DNA (mtDNA) cytochrome c oxidase I gene (COI) to clarify the genetic structure of the small yellow croaker, Larimichthys polyactis, in the Yellow and East China Seas, especially regarding four provisional populations, (one Korean and three Chinese populations). Based on microsatellite DNA variations, the estimated expected heterozygosity ($H_E$) in each population ranged from 0.776 to 0.947. The microsatellite pairwise $F_{ST}$ estimates showed no significant genetic differentiation between the populations. MtDNA variations also indicated no genetic structure in L. polyactis, but very high variability. The absence of genetic differentiation among and within populations of L. polyactis may either result from the random migration of the adult or the passive dispersal of the eggs and larvae.

• Animal Systematics, Evolution and Diversity
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• 제14권2호
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• pp.135-157
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• 1998

우리 나라 남해 서부 연안에서 1996년 4월부터 1997년 3월까지 월 1회 어류를 조사하여 19목 82과 149속 190종을 채집하였다. 그 가운데 농어목은 94종이 출현하여 전체 출현종의 49%를 차지하였다. 채집된 어류중 두줄망둑 Tridentiger trigonocephalus, 실양태 Repomucenus valenciennei 및 풀반댕이 Thryssa adelae가 가장 우세하게 출현하였다. 또한 황해고유종인 왜도라치 Chirolophis wui, 흰베도라치 Pholis faugi, 참돛양태 Repomucenus koreanus, 비늘흰발망둑 Acanthogobious luridus 등이 출현하여 이 지역은 황해의 영향권에 있음을 알 수 있었다.

• 한국동물위생학회지
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• 제39권4호
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• pp.271-276
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• 2016

Horsehair or gordian worms (Nematomorpha) were identified with 22 genera (Gordiida) and 5 marine species (Nectonema) until now. During juvenile phase in development, they gain parasitic activity in arthropods. In this study, a gordian worm was detected in the feces of a dog living in Nonsan-si, Chungcheongnam-do, Korea. Using this worm, we evaluated the morphological characteristics by light microscopic analysis. Furthermore, the morphological classification was re-evaluated by scanning and transverse electron microscopes. The worm was determined that it is male adult having a bi-lobed tail and male gonads in cross sections. Based on the morphological characteristics including cross sections of body and areole on the cuticle, the parasite was also identified as Gordius sp. (Nematomorpha: Gordiidae).

• Animal cells and systems
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• 제7권1호
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• pp.57-62
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• 2003

Flounder B lymphocytes isolated from different tissues were studied in terms of cell proliferation, apoptosis and the effects of cortisol on these processes. B lymphocytes, isolated from the flounder head kidney and spleen, were characterized by higher proliferation and lower intracellular calcium ($Ca^2$) response to lgcrosslinking compared with peripheral blood B lymphocytes. Cortisol induced high levels of apoptosis (150% of control levels) in peripheral blood B lymphocytes, in combination with a stimulatory LPS signal. Head kidney and to a lesser extent spleen B lymphocytes, although less sensitive than their equivalent in peripheral blood, underwent cortisol-induced apoptosis irrespective of extra stimulation up to 142% of control levels. Also proliferation with and without LPS stimulation was suppressed by cortisol (compared to plasma values measured during stress conditions) that is effective in inducing a significant increase in apoptosis in all three populations of B-cells, suggesting that cortisol may be important for immunoregulation in both stressed and non-stressed conditions. This implies possible severe impact of stress on lymphocyte development and activity, Different sensitivity of B-cells to the corticosteroid, with respect to developmental stage and activity, may prevent excessive and long lasting depletion of B-lymphocytes.