• The Korean Journal of Mycology
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• v.13 no.2
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• pp.115-121
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• 1985

An aerial survey for fungal flora in Seoul has been carried out by Petri plate exposure method for a period of one year. A total of 2227 fungal spores appeared in the plates. Of these, Cladosporium was the commonest fungus representing 43.5% of the total spore count followed by Penicillium (15.8%). Alternaria (10.5%), and Aspergillus (3.8%). There were seasonal variations in the prevalence of fungal spores. The occurrence of these fungi was greatly affected by climatic conditions. However, Alternaria appeared to prefer warmer weather. A comparison of fungal population from the outdoor and indoor air was also investigated to support the view that Alternaria is abundant population from the outdoor air and that Cladosporium from the indoor air depending on their availability in the atmosphere.

• Journal of Forest and Environmental Science
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• v.30 no.3
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• pp.277-284
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• 2014

Status of Arbuscular Mycorrhizal (AM) colonization in seven tree species (Albizia saman, Acacia auriculiformis A. Cunn. ex Benth., Albizia lebbeck, Chickrassia tabularis A. Juss., Eucalyptus camaldulensis Dehnn., Gmelina arborea (Roxb) DC, Swietenia macrophylla King.) collected from the hilly areas of Chittagong University (CU) was investigated. Roots and rhizosphere soil samples were collected in different seasons (pre-monsoon, monsoon and post monsoon). Percentage of AM colonization in root and number of spores/100 gm dry soil were assessed. The result of the investigation reveals that the intensity and percentage of AM colonization varied in different forest tree species in different seasons. In this study, maximum AM colonization and spore population were found in pre-monsoon and minimum were in monsoon season. The intensity of colonization was maximum in C. tabularis (74.43%) in pre-monsoon, A. lebbeck (69.45%) in monsoon and S. macrophylla (67.8%) in post monsoon seasons and minimum in A. auriculiformis (53.75%) during pre-monsoon, A. saman (24.4%) in monsoon and A. saman (19.36%) in post monsoon. The number of spores found per 100 g dry soil ranged between 164-376 during pre-monsoon, 27-310 during monsoon and 194-299 in post monsoon season. Out of six recognized genera of AM fungi, Glomus, Sclerocystis, Entrophospora, Scutellospora, Acaulospora and other unidentified spores were observed.

• The Plant Pathology Journal
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• v.15 no.4
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• pp.158-161
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• 1999

We determined threshold environmental factros to initiate infection of pepper plants by Botrytis cinerea, a fungal pathogen of pepper gray mold, in two greenhouse conditions. A new efficient spore-trapping method was developed to estimate population density of airborne conidia in the greenhouses, and spore release was measured using a Kerssies' selective medium. At a given day, spores were released greater during daytime (mostly from 7:30 am to 10:30 am and at 4:30 pm) than nighttime. Diurnal and nocturnal temperatures in the greenhouse-1 were about $25^{\circ}$ and $17^{\circ}$,and relative humidity was 100% for prolonged 24 h due to rain on December 17, 1997. Population density of air-borne conidia was 3.0$\times$103 conidia/ $0.5\textrm{m}^3$ after two days, and the initial infection occurred in ten days. During the same period of time in the greenhouse-2, diurnal temperature was about $25^{\circ}$ and nocturnal temperature was below $15^{\circ}$, and population density of air-borne conidia was 104 conidia/ $0.5\textrm{m}^3$. Under these conditions, the initial infection started in three days. This indicates that the early infection occurs under which diurnal temperature is approximately $25^{\circ}$, nocturnal temperature is maintained below $15^{\circ}$, and population density of air-borne conidia is 104 conidia/ $0.5\textrm{m}^3$ at saturated relative humidity condition.

• Journal of Crop Science and Biotechnology
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• v.11 no.2
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• pp.101-106
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• 2008

To identify inheritance of clubroot disease resistance genes in Chinese cabbage, seedling tests of $BC_1P_1,\;BC_1P_2$, and $F_2$ populations derived from $F_1$ hybrid(var. CR Saerona) using single spore isolate(race 4 identified with William's differential host) from Plasmodiophora brassciae were conducted. Resistance(R) and susceptible(S) plants segregated to 1:0 in backcross to the resistant parent. The $F_2$ population segregated in a 3(R):1(S) ratio. This result implied that the resistance of clubroot disease is controlled by a single dominant gene to the race 4 of P. brassicae in CR Saerona. To develop DNA markers linked to clubroot resistance genes, 185 plants of CR Saerona among $F_2$ populations were used. A total of 300 arbitrary decamer was applied to $F_2$ population using BSARAPD(Bulked segregant analysis-Randomly amplified polymorphic DNA). One RAPD marker linked to clubroot resistance gene in CR Saerona($OPJ_{1100}$) was identified. This marker was 3.1 cM in distance from resistance gene in $F_2$ population. This marker may be useful for a marker-assisted selection(MAS) and gene pyramiding of the clubroot disease resistant gene in Chinese cabbage breeding programs.

• The Korean Journal of Mycology
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• v.45 no.4
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• pp.328-335
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• 2017

In this study, we made a population with high biological efficiency (BE) to investigate the complex genetic architecture of yield-related traits in Agaricus bisporus. MB-013 crossed between bisp 015-p2 and bisp 034-p2, had high BE. Additionally MB-013 was an intervarietal hybrid that intercrosses with A. bisporus var. burnettii, bisp 015, and A. bisporus var. bisporus, bisp 034. One hundred and seventy homokaryons were selected using the cleaved amplified polymorphic sequence (CAPS) markers (PIN primer/HaeIII) from 300 single spore isolates (SSIs). One hundred $BC_1F_1$ hybrids were obtained by crossing the homokaryons of MB-013 with bisp15-p1. The population of 100 BC1F1 hybrids is suitable for analyses of BE.

• Korean Journal Plant Pathology
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• v.14 no.6
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• pp.710-713
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• 1998

Spatial distribution in soil and seasonal population changes of Pasteuria nishizawae first found in Korea from soybean cyst nematode were studied. P. nishizawae infested in 61% of areas in a soybean field; in an average, about 0.3% of 46 cysts and 17.6% of 9 juveniles per 100 g soil were infested with the bacterium. The highest percentages of spore-attached nematodes were found in July (75%) and between soil depth of 11~20 cm. The number of spores per juvenile was positively correlated with the percentage of juveniles with spores (r=0.4203; P＜0.0133), but negatively correlated with the number of juveniles in soil (r=-0.3499; P＜0.042). P. nishizawae completed its life cycle in cyst and produced 1.7$\times$105 spores per cyst.

• Korean Journal of Plant Resources
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• v.16 no.1
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• pp.40-48
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• 2003

Cylindrocarpon destructans is the major pathogen inducing the root rot disease in ginseng. Up to now, there is no reliable and convenient method to analyze the spore density or population of this pathogen in ginseng-growing soil or any contaminated farmlands. Therefore, it will be very valuable to develop a new and reliable method in detecting the spore of this pathogen. In this study, a molecular biological technique using two step nested PCR method, was developed. Two universal ITS primers, ITS5F and ITS4R were used in the first round of PCR to amplify a fragment of ITS region from the genomic DNA of C. destructans. The specific prmers Nest 1 and Nest 2 were designed and used in the second round of PCR to amplify a inner fragment from the first round PCR product of C. destructans. C. destructans spore, only soil samples from the diseased ginseng farm produced the positive bands, suggesting its usefulness in detecting the C. destructans spores in soil samples. Thus it is recommended to first extract the whole genomic DNA from soil samples and use it for the PCR reaction, thereby eliminating the inhibitory activity of soil components.

• Korean Journal of Microbiology
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• v.33 no.1
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• pp.7-14
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• 1997

This study was to elucidate the relation between the periodical requirement of growth factors(Yang et al., 1993) and the synthesis of RNA and protein during the germination of Streptomycn coefic%r A3(2) in mineral liquid medium(ISP-4) without addition of growth factors. As results, The germination time was about 10 hr, and meanwhile, periodical nutritional requirement was verified to be repeated with interval of 2 hr. Spore size was enlarged with time but its number was rather decreased. Spore could be deviJed into viable, dormant, and dead state. In such a germination process it was found that RNA and protein were being synthesized periodically when spores were stained with AO and INT methods and observed under the fluorescence microscope. Those syntheses were coincided with the period of nutritional requirement. Hence, it was discllssed that spore population in early germination would need amino acids related to protein synthesis.

• International Journal of Industrial Entomology and Biomaterials
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• v.27 no.2
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• pp.282-288
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• 2013

In nature, the population of Nosema bombycis (Microsporidia) causing pebrine disease is small and their development is extremely slow and only few ultimately producing spores. Pebrine infected silkworm, Bombyx mori larvae collected from sericulture field were alive till $3^{rd}$ generation though the concentration of N.bombycis spore was very high ($2.4-3.0{\times}10^8$ spores. $mL^{-1}$). All larvae were died during $4^{th}$ generation with extremely high concentration of pebrine spores ($3.0-4.0{\times}10^9$ spores. $mL^{-1}$) and mostly contain long polar tube (LT). Alternately, all larvae were died immediately (at $3^{rd}$ stage of $1^{st}$ generation) when it was artificially inoculated with same concentration of N.bombycis spores harvested from field ($2.4-3.0{\times}10^8$ spores. $mL^{-1}$) though concentration of spores harvest was very less ($3.0-4.0{\times}10^6$ spores. $mL^{-1}$) and mostly contain short polar tube (ST). Artificially pebrine infected male moth when mated with healthy female moth took six generations to develop pebrine disease and all larvae were died at the $2^{nd}$ stage with very less spore harvest ($3.0-10.0{\times}10^6$ spores. $mL^{-1}$). Survival percentage was increased in all generations (~92.0% at $4^{th}$ generation) when silkworm rearing was conducted under new integrated disease management system.

• Proceedings of the Korean Society of Plant Pathology Conference
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• 2003.10a
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• pp.112.1-112
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• 2003

Genetic diversity of Plasmodiophora brassicae from major chinese cabbage cultivating areas in Korea was analyzed by using PCR-RFLP and RAPD. Single spores of P brassicae isolated from galls of club root made induce lesion on chinese cabbage successfully. The PCR-RFLP and RAPD by primers PbITS, URP 3, 6 and OPA 7 revealed that single spore isolates showed various DNA polymorphisms among them unrelated geographic origins. These results indicate that P. brassicae population in Korea showed genetic difference among them. This study could be facilitate to identify genetic characteristics ofP. brassicae based on DNA polymorphisms between single spore isolates and to get basic information which can be used to advanced resistance breeding against club root of chinese cabbage.