• Korean journal of applied entomology
• /
• v.23 no.1 s.58
• /
• pp.37-41
• /
• 1984

The $100\%$ of insect pests on the imported logs and Sitophilus oryzae(L.) will be killed both when the imported logs are fumigated on shipboard with 25g methyl $bromide/m^3$ for 24hours at $10\~20^{\circ}C$ and when they are fumigated on shipboard with 37.5g methyl $bromide/m^3$ caculated by DT products for 16 hours at $10\~20^{\circ}C$ using 2 fans of 1800rpm over and ID 30cm. Without using fans, it takes $4\~6$ hours to make gas concentration even in hold. But using 2 fans per hold, the period reduces to $1\~3$ hours.

• Horticultural Science & Technology
• /
• v.30 no.3
• /
• pp.236-242
• /
• 2012

We investigated the influences of night interruption (NI) and night temperature on flowering and flower coloration in Cymbidium. Cymbidium 'Red Fire' and 'Yokihi' were grown under a 9 hours photoperiod (control), a 9 hours photoperiod with NI at a low light intensity (LNI) of 3-7 ${\mu}mol{\cdot}m^{-2}{\cdot}s^{-1}$, or a 9 hours photoperiod with NI at a high light intensity (HNI) of 120 ${\mu}mol{\cdot}m^{-2}{\cdot}s^{-1}$ for four hours (22:00-02:00 HR) for 16 weeks during the reproductive growth stage (Experiment 1). Thirty month-old Cymbidium 'Red Fire' plants with initiated flowering buds were placed in four different growth chamber with night temperature set points of 6, 9, 12, or $15^{\circ}C$ for 16 hours (18:00 to 09:00 HR) and a daytime temperature of $25^{\circ}C$ (Experiment 2). In Experiment 1, the numbers of visible buds and flowers increased, and time to flowering decreased in both the LNI and HNI treatments, as compared to the control in both cultivars. Red color in Cymbidium 'Red Fire' increased by both LNI and HNI, as evidenced by an increased $a^*$ in plants grown under these conditions, relative to those grown under the control condition. Number of days to visible buds at 9-$15^{\circ}C$ ranged from 31-34 days, as compared to 39 days at $6^{\circ}C$ in Experiment 2. Although as the temperature increased days to flowering decreased when the plant was grown at $15^{\circ}C$ as compared to 6, 9, or $12^{\circ}C$, the red color ($a^*$) also decreased. The number of flowers and percent flowering increased when the night temperature was maintained higher than $9^{\circ}C$. Therefore, NI treatment and maintaining the night temperature at approximately 9-$12^{\circ}C$ during the winter season after flower spike initiation in the reproductive developmental growth stage improve flower quality and controls flowering time.

• Journal of Plant Biology
• /
• v.32 no.3
• /
• pp.189-201
• /
• 1989

In this study, genus Cosmarium, 3 species, 2 varieties, 1 forma were sampled at 14 stations from August 1987 to July 1988. The character variations in populations were studied from the cultured plants. As a result, 1 species, 1 variety and 1 forma were treated as synonyms according to the polymorphism found at the same colony. C. angulosum f. rotundatum was different from C. angulosum by the front view, but C. angulosum type and C. angulosum f. rotundatum type occurred simultaneously in the same colony. C. angulosum f. rotundatum was included in C. angulosum which is type species. c. auriculatum, C. subauriculatum and C. subauriculatum var. truncatum have been sorted by the shape of cell and the number of granules at the lower sides of semicell. For three types occurred at the same colony, those species and variety treated as synonym of C. auriculatum which was named first.

• Applied Biological Chemistry
• /
• v.51 no.1
• /
• pp.65-69
• /
• 2008

The roots of Brassica campestris ssp rapa were extracted with 80% aqueous MeOH, and the concentrated extract was partitioned with EtOAc, n-BuOH and $H_2O$. From the EtOAc fraction, three compounds were isolated through the repeated silica gel and octadecyl silica gel (ODS) column chromatography. From the results of spectroscopic data including NMR and MS, the chemical structures of the compounds were determined as caulilexin C (1), indoleacetonitrile (2) and arvelexin (3). The arvelexin (3) has been isolated from this plant for the first time. Compounds 1, 2 and 3 showed inhibitory activity on human Acyl CoA: cholesterol. transferase 1 (hACAT1) by $54.6{\pm}6.0%$, $69.2{\pm}4.7%$ and $68.6{\pm}3.7%$, and on human Acyl CoA: cholesterol transferase 2(hACAT2) by $4.8{\pm}13.4%$, $45.6{\pm}4.8%$ and $39.5{\pm}4.3%$, respectively, at 100 ${\mu}g/ml$.

• Korean Journal of Plant Taxonomy
• /
• v.49 no.3
• /
• pp.269-273
• /
• 2019

We report the meiotic chromosome numbers of four Carex taxa from Korean populations. Three are the first reports made on taxa from Korean populations: Carex appendiculata (Trautv. & C. A. Mey.) $K{\ddot{u}}k$. ($n=27_{II}$), C. fernaldiana H. $L{\acute{e}}v$. & Vaniot ($n=33_{II}$), and C. metallica H.$L{\acute{e}}v$. ($n=15_{II}$). Reports on the other species expand the range of variation in the chromosome number within a taxon, C. miyabei Franch. (n = $43_{II}$, $44_{II}$, $45_{II}$). Carex L. (Cyperaceae) consists of more than 2,000 species worldwide and is the most species-rich genus in Korea. The species diversity in the genus has been hypothesized to be associated with the chromosome variation, but chromosome information pertaining to Korean Carex taxa is not well known. This report updates the chromosome number inventory on Korean Carex to 24 out of 180 taxa.

• Proceedings of the Korean Society of Crop Science Conference
• /
• 2022.04a
• /
• pp.21-21
• /
• 2022

• Proceedings of the Korean Society of Crop Science Conference
• /
• 2021.10a
• /
• pp.199-199
• /
• 2021

• Proceedings of the Korean Society of Crop Science Conference
• /
• 2021.04a
• /
• pp.112-112
• /
• 2021

• The Plant Pathology Journal
• /
• v.17 no.4
• /
• pp.216-221
• /
• 2001

Dieback of pine branches or twigs with brown needles occurs most commonly on Pinus species after severe winter in Korea. In this study, Cenangium ferruginosum was isolated from infected stems, branches, and twigs of Pinus koraiensis (C1), P. densiflora (C2), and P. thunbergii (C3). Morphological and cultural characteristics of the isolates were than compared. There were no significant differences in the morphological characteristics of conidia and ascospores produced by the three isolates. However, cultural differences were observed among the isolates. Optimum temperatures for mycelial growth of C1, C2, and C3 were 15, 20, and $20^{\circ}$, respectively. C1 produced a few conidia and no ascospores, while C2 and C3 produced abundant ascospores and conidia. While optimum temperatures for mycelial growth ranged from 15 to $20^{\circ}$, mycelial growth was also relatively good at lower temperatures of 5-$10^{\circ}$. Conidiomata and conidia were produced on MSA (malt extract soya peptone agar) after 25-30 days of incubation in the dark at $15^{\circ}$. Apothecia were produced by altering culture condition from 15 to $20^{\circ}$, and incubating for 35-60 more days. Optimum temperature for ascospore and conidium germination was $20^{\circ}$. RAPD analysis revealed that there was high similarity of 0.78 between C2 and C3, and low similarity of 0.31 between C2 or C3 and C1.

• The Plant Pathology Journal
• /
• v.18 no.4
• /
• pp.187-191
• /
• 2002

This paper describes the cloning and sequence analysis of the 5'-terminal region and full-length cDNA production of genomic RNA of Lily symptomless virus (LSV), a Species Of the genus Carlavirus. A sing1e DNA band about 600 bp harboring the 5'-end of genomic RNA of the virus was successfully amplified by reverse transcription-polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends (RACE), and was cloned for nucleotide sequence determination. Sequence analysis of selected RACE cDNA clones revealed that the LSV 5'non-translated region consists of 67 nucleotides long of AT rich stretch followed GC rich from the 5'-end. To produce full-length cDNA products for the viral genomic RNA, a set of LSV-specific primers could be designed based on the obtained sequence in this study and the known sequences of 3'-terminal region for the virus. Full-length cDNA copies of LSV, an 8.4 kb long, were directly amplified by the long-template RT-PCR technique from the purified viral genomic RNA samples. This full-length cDNA copies were analyzed by restriction mapping. The molecules produced in this study can be useful for the production of in vitro infectious cDNA clone, as well as, for the completion of genomic RNA sequence and genome structure for the virus.