• Title/Summary/Keyword: Cellular slime mold

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A Study on the Distribution and the Effect of Torreya Fruit Extract on Cellular Slime Molds in Torreya Forest of Cheju Island (제주도 비자림에서의 세포성 점균의 분포 및 비자열매 추출액의 성장 효과에 관한 연구)

  • 최선영;장남기
    • Asian Journal of Turfgrass Science
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    • v.10 no.3
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    • pp.187-194
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    • 1996
  • Dictyostelid cellular slime molds were isolated from soils and harks of the subtropical forest of Torreya nucifera in Cheju island. The results were as follows: Polysphondylium pallidum,Dictyostelium purpureum, D. mucoroides, D. aureo-stipes var. aureo-stipes, D. flavidum, D. miniutum, P.violaceu m, D. monocrhasioides. D. brefeldianum, D. polvcephalum. D. areum var. areum, P. tenuissimum, D. fasciculatum. In this forest, P. pallidum and D. purpureum were occurred dominantly, and D. mucoroides and D. aureo-stipes var, aureo-stipes were the second dominant. It was distinguished that D. purpureum was much more cornmonly found than the other forests. Cellular slime molds from the barks of the tree heights of 1,3 and 5m were occured 7, 3 and 2 species respectively. Torreya fruit extract affected on the growth of D. aureo-stipes var. aureo-stipes and D. flavidum but not on D. purpureum and D. mucoroides. Key words: Cellular slime mold, Torreya forest, Torreya fruit extract.

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The Distribution of Cellular Slime Molds in Forests of Seoul Area and Relationship between Cellular Slime Molds and Soil Microorganisms (서울지역 삼림에서 세포성 점균의 분포와 토양 미생물과의 관계)

  • 홍정림;장남기
    • Asian Journal of Turfgrass Science
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    • v.10 no.3
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    • pp.247-262
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    • 1996
  • In this study, the distribution of dictyostelid cellular slime molds was investigated from F, H and $A_1$ horizon of pinus, oak forests in Mt. Puk'an, Mt. Nam and Mt. Kwanak. The relationship of cellular slime molds with other soil microorganisms and abiotic factors were analyzed. The six species were isolated as follows: Polysphondlium pallidurn, Dictyostelium purpureum, D. mucoroides, D. crassicaule, D. capitatum, D. implicatum. The dominant species in pinus forests was P. pallidum, and in oak forests it was D. macro ides. In Mt. Nam, D. mucoroides and P. pallidum were isolated at only oak forest. The Correlations of slime mold abundance with bacteria were significant. Even though positive correlations of cellular slime molds with actinomycetes or fungi were not significant, correlations between soil microorganisms were analyzed. Correlation coefficients were high in Mt. Kwanak(r=0.5921) and Mt. Nam(r=0.7243) at significant level P<0.01. There were significant correlations between total slime molds and abiotic factors. It supports that cellular slime molds are limited by foods in nature. In low level of pH, water content and organic matter, that community diversity is more affected by bacteria whose organic degradation capacity is regulated by interactions of soil microorgaisms. Key words: Cellular slime molds, Soil microorganisms, Correlations, Abiotic factors.

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Cellular Slime Molds in the Littoral Grassland Ecosystems in the Lake Paldangho (팔당호 연안대 초지생태계의 세포성 점균)

  • 심규철;장남기
    • Asian Journal of Turfgrass Science
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    • v.11 no.2
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    • pp.125-137
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    • 1997
  • Five dictyostelid cellular slime molds were isolated from the littoral grassland ecoystems of the lake Paldangho, safeguard of waterworks, Kyounggi-do, South Korea. They were Poiysphoadylium violceum, Dictyosielium aureo-stipes var. aureo-stipes D crassicaule, D macrocephalum and D gigauteum. P. violaceum was dominant species. It live on the low nutrient and barren soils as the littoral zone destabilized in surface soils, litters and chemicals by inundation an rain precipitation. Key words: Cellular slime mold, Littoral grassland ecosystem.

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The Occurrence and Morphological Comparison of Dictyostelid Cellular Slime Molds in Mt. Muhak Soils

  • Hwang, Ji-Young;Hiromitsu Hagiwara;Kim, Jong-Hee
    • The Korean Journal of Ecology
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    • v.23 no.4
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    • pp.315-321
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    • 2000
  • The occurrence and distribution of Dictyostelid cellular slime molds on Mt. Mukak soils with two different vegetation types were investigated. Two plating methods were used for the isolation of dictyostelids following Dr. Hagiwara's method. Dictyostelium and Polysphondylium were isolated in these soils. D. purpureum (subtropical form ) and D. giganteum were observed in both Quercus variabilis and Pinus thunbergii communities soils. D. delicatum, B. sp-1 (D. brefeldianum complex). D. sp-2 (D. brefeldianum complex), D. minutum and P. pallidum complex occurred only in Q. variabilis soil. D. macrocephalum, D. purpureum (temperate form ), D. robustum, D. polycephalum, P. violaceum, and P. pallidium occurred only in P. thunbergii soil. P. pallidium complex is being identified.

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New Dictyostelid in Mt. Surak, Korea;Dictyostelium valenstemmum sp. nov. (한국산 세포성 점균의 신종 : Dictyostelium valenstemmum sp. nov.)

  • 심규철;장남기
    • Asian Journal of Turfgrass Science
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    • v.10 no.2
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    • pp.117-124
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    • 1996
  • One new cellular slime mold, Dicivostelium valenstemmun sp. n. Shim et Chang, is isolated from the fermentation layer of soils in the cool temperate forests of Surak mountain, Korea. This species has the sori and sorophore yellow-pigmented, and sparse or irregular branches. And it is characterized by tall and robust sorocarps, well-form basal disks, mucoroides-type aggregations and large spores. This species has sorophores gradually tapering from bases to tips, simple capi- tate sorophore tips and conical bases. When prostrates on the plates, it has sparsely clavate bases. Spores are considerably large, 6.8~9.9 x 3.4~5.1 $\mu$m(avg. 8.5 x 4.1 $\mu$m), L /W index l.84~2.43(avg. 2.07) without polar granules. Key words: Diccyostelium valeustemmum, Cool temperate forests, Surak mountain.

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Ecological Evolution by Competitive Exclusion / An Experimental Approach with Cellular Slime Mold , Polysphondylium pallidum (경쟁배타에 의한 생태적 진화: 세포성 점균 Polysphondylium pallidum에 대한 실험적 접근)

  • ;Robert M. Eisenberg
    • The Korean Journal of Ecology
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    • v.17 no.3
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    • pp.299-310
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    • 1994
  • Intraspecific clonal interactions have important influences on a population structure of the cellular slime mold (CSM). This study was to investigate whether or not evolutionary change in a population could be induced by clonal competition, and to elucidate how various clones in a population evolve in a homogeneous environment of laboratory culture. The characteristic clones of Polysphondylium pallidum which had different resource consumption rates (RCR) and mating types I and II were selected for study. Investigation was conducted for 4 experimental time interval $(T_0-T_4)$; one experimental time interval took almost 10-14 days from inoculation to havest of fruiting bodies. Two sets of 50 clones were cultured from 50 clones at To, and RCR variations of the population were compared between $(T_0\;and\;T_4)$ for each set of clones. Each clone of the CSM had a diverse resource consumption rate, or growth rate, in a homogeneous and limited Cerophyl agar plate despite the passage of 48-56 generations from the beginning of the experiment. Diverse clones with different growth rate could coexist in one site of the homogeneous agar plate as well as heterogeneous soil microenvironment. When there was high clonal diversity of RCR, a clone in a population had high chances to encounter other clones with resultant increased clonal competition. In one set, 26 of 37 clones of mating type I were changed to mating type Il for the 4 experimental time intervals, which indicated that the rate of competitive exclusion among clones during total experiment from $(T_0\;to\;T_4)$ was 0.703. In another set, 31 of 37 clones of mating type I were changed to mating type II , having the rate of competitive exclusion 0.838. The frequency of each of mat~ng types changed by 0.93-1.29% in each successive generation. The competitive exclusion among clones occurred by 1.26-1.75% when approximately $2.6{\times}10^8$ bacterial cells were provided as food and thereafter one generation of myxamoebae of CSM elapsed at room temperature. This finding implicated that in the vegetative state of P, pallidurn there was 1.26-1.75% probabil~ty of evolutionary change per generation changing from one clone to another clone.

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