• Journal of Forest and Environmental Science
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• v.34 no.6
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• pp.435-450
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• 2018

Phenological events of four Rhododendron tree species (viz. R. arboreum, R. arboreum ssp. delavayi var. delavayi, R. barbatum and R. kesangiae) was monitored in temperate mixed broad-leaved forests of Arunachal Pradesh, India. Phenological events like flower bud formation, flowering, fruit setting, fruit maturing, seed dispersal, leaf bud formation, leaf flushing, and leaf shedding were recorded. Indices i.e., phenophase sequence index (PSI), active phenophasic period of the species (APS) and index of reproductive/vegetative activity (RVA) were also calculated. Present study revealed that bark consistency, growth form and leaf pattern of the studied species have showed variations among the species. Rhododendron species exhibited the phenological events overlapping with other phenophases. The peak flower bud formation was observed during the winter; R. arboreum ssp. delavayi var. delavayi start flowering from December, while the flowering in rest three species exhibited during February to April. Fruit setting occurred during summer to autumn while fruit maturation revealed peak during November. Leaf bud formation illustrated two peaks in April and May, leaf flushing exhibited peak in June, while leaf shedding peaked during October to November. Active phenophasic period of the species were found 12 months, which revealed that species engage in various phenophase activities throughout the year. Phenophase sequence index ranged between 0.8 to 0.9 (PSI ${\geq}0.6$), signifies that species have a sequential arrangement of phenophases. Index of reproductive/vegetative activity of the species exemplified >1, indicate that the reproductive phenophases were dominance over vegetative phenophases. The study have provided substantial insight on the life cycle events of Rhododendron species and ecological approaches for further scientific study with recent climate change and effective management and conservation.

• Korean Journal of Agricultural and Forest Meteorology
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• v.15 no.3
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• pp.191-200
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• 2013

This study was conducted to examine the geographic variation of bud phenology of Zelkova serrata provenances. Data were collected from Gangneung, Yilmsil, Hwaseong and Jinju plantations which were parts of the 6 provenance trials established by Korea Forest Research Institute in 2009. The 16 provenances were included in these trials. The starting date of bud burst and finishing date of leaf expansion were investigated from April to May every other day. The four geographic factors and fifteen climatic factors of the test sites and provenances were considered in this study. Canonical correlation analysis was conducted to examine the major factors affecting the bud phenology between test sites and provenances. The study results suggested that the major factors affecting the timing of bud burst were the differences of extremely high temperature (March-October), annual mean temperature, mean temperature (March-October), extremely high temperature (July-August) and mean humidity (June-October) between test site and provenance. The provenances with lower mean or high temperature than those of plantation showed the earlier bud burst and leaf expansion. It showed a typical north-south or low-high temperature cline. Finally, we discussed the implication of the tree breeding program of Z. serrata based on these results.

• Journal of Bio-Environment Control
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• v.20 no.1
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• pp.45-49
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• 2011

This research was carried out to investigate frost damage of mulberry tree (Morus alba) according to topographic characteristics in Buan province. The first bud-break, leafing, blooming and harvest date of mulberry tree in 2010 were two, four, fourteen and eight days later than those in 2009, respectively. These results were that daily mean temperature during March and April in 2010 were lower than those in 2009 by $2.3^{\circ}C$ and $2.4^{\circ}C$. Frost damage of orchards at flat-bottomed valley, flat near hill and lake, and plain were 50.0%,12.0%, and 4.2%, respectively. Also, frost damage of branch of below 15 mm in diameter was serious than that of branch over 16 mm, but orchard at flat-bottomed valley was high as the range of 46.2~54.0%. These results in 2010 were caused by occurrence of below zero temperatures in leafing stage. Since then, many shoots came out at accessary bud on proximal and the top part of the branches. Therefore, frost damage of mulberry tree in Buan province in 2010 was caused by occurrence of below zero temperatures on April and topographic characteristics of orchard.

• Korean Journal of Environmental Agriculture
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• v.37 no.2
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• pp.87-96
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• 2018

BACKGROUND: The vigorous shoot growth in upper part of apple tree canopy leads to poor fruit quality and flower bud formation in lower part of canopy. So, this study was conducted to develop the proper control method about the shoot growth in upper part of apple tree canopy. METHODS AND RESULTS: Trunks of 'Fuji'/M9 apple trees were cut (back pruned) to 2.5 m in tree height on 11 February (dormant) or 12 April (full bloom). Naphthalene acetic acid (NAA) was applied at 2.0% to cut surface when trunk was pruned. Prohexadione-calcium (Pro-Ca) was sprayed at 250 mg/L above 2.0 m in tree height at 23 April (petal fall). The NAA or Pro-Ca application after trunk was pruned at dormant (TR-2 and TR-3) significantly reduced shoot growth in upper part of canopy compared with the control (tree was only pruned at dormant, TR-1), but the percent of shoots showing the secondary growth of TR-3 was higher over 2 times than that of TR-2. The reduction of shoot growth in upper part of canopy by TR-2 and TR-3 increased the fruit red color from the lower part in the treating year and blooming of the lower part in the following year. CONCLUSION: Applying 2.0% NAA to cut surface of pruned apple trunk at dormant was the most effective way for stabilization of the tree vigor in upper part of the canopy in a high density apple orchard.

• Horticultural Science & Technology
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• v.33 no.4
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• pp.501-510
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• 2015

In this study, we investigated the onset and release of endo-dormancy under natural conditions by observing bud break characteristics in 'Fuji' apple trees using water cuttings. Through examinations of bud break rate and days to bud break, we found that the endo-dormancy of 'Fuji' apple tree continues for 70 d from 165 to 255 d after full bloom (DAFB), from late October to early January of the following year. In addition, within 20 d of first bud break, based on a final bud break rate of 60% or more, we able to identify the timing of the changeover from para-dormancy to endo-dormancy, and endo-dormancy to eco-dormancy. Analysis of the chilling requirement during the endo-dormancy period revealed that chilling accumulation up to 255 DAFB to release endo-dormancy amounted to 666 and 517 h based on the CH and Utah models, respectively. Observation of internal changes in the bud during endo-dormancy showed that flower bud differentiation begins from mid-July, and t ime of inflorescence o f the disk f lower is a vailable to f ind. The f lower buds subsequently developed slowly but steadily during endo-dormancy and in the following year in February, the developmental stage of each organ had progressed. Moreover, the flower buds of 'Fuji' apples were mostly healthy during the dormancy period, but some exhibited necrosis of flower primordium, due partial cell damage from the formation of ice crystals rather than a direct effect of the low temperature. Flower buds were formed in both the axillary buds of bourse shoots and terminal buds of spurs, but lower bud differentiation was observed for the terminal buds of spurs at rate of about 65% of total buds, which was directly related to the bud size and shoot diameter.

• Journal of Korean Society of Forest Science
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• v.40 no.1
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• pp.57-62
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• 1978

This study was carried out to determine the proper transplanting time of Platanus occidentalis L. (plane tree, sycamore) with 5 to 6 cm and 25 to 30 cm in diameter of breast height at the forest nursery of Chonnam National University in 1977. For that purpose, the experiment of the time of transplantation, and the moisture content and soluble sugar were analysed. The results are as follows: 1. Both its rooting and growth were slightly different in the period of January to early April (before bud-break), but remarkably declined after its bud-break (mid-April to May). 2. And also, its moisture content and soluble sugar were slightly different (January to early April), but, on the other hand, considerably increased in the content of moisture and sharply decreased in soluble sugar after bud-break (mid-April to May). 3. In comparision with healthy trees, rooting and growth of trees infected with Cankers were unusually retarded and its moisture content and soluble sugar were much less. 4. The proper time to plant sycamore was recognized to be the period of November to March, since the higher amounts of soluble sugar and the lesser amounts of moisture in that period. 5. The sudden exposure to the sun of the boles of diseased and wounded trees could be in death in case of sun-scald on the side of south-west. 6. Pruning wounds should be treated with an antiseptic, as soon as they are made, to prevent entrance of decay or disease while the wound is healing. 7. The wound and sun-scald can be presented by covering the trunk with straw ropes before transplantations.

• Horticultural Science & Technology
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• v.19 no.4
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• pp.540-544
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• 2001

The effect of long day treatment on the growth and flower bud differentiation of persimmon tree grown in a heated plastic house was investigated. The rate of leaf sprout was 65% in the long day treatment and 71% in natural day (control). In the long day, the shoot grew 16.7 cm longer, full bloom and harvest days were shorter, fruit weight was 16% lighter, and the sweetness and firmness of fruit were lower. The photosynthesis rate in the long day treatment was higher, showing the tendency of increasing with time. However, the rate of photosynthesis increased after 1600 hours showed higher than the control. Carbohydrate accumulation in the shoot was decreased, with higher nitrogen content and lower C/N ratio in the long day. The number of flower primordia per bud was less, and the days for differentiation was longer in the long day.

• Journal of Korean Society of Forest Science
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• v.79 no.4
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• pp.431-434
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• 1990

The growth pattern of bud-shoot-needle of isolated 15-year-old trees, and seansonal changes in litter-falls and fine root dry weights in the unthinned 28-year-old plantation were investigated to understand the growth phenology of Pinus koraiensis. Shoot growth was continued by 7th June when buds appeared, while current needle growth was by 19th July when the bud growth started. Most of the litter-falls occurred in October but many of them were fallen in July and August due to storms, Fine roots were produced mostly in autumn(1,004 kg/ha), and were dead during winter (583 kg/ha) and spring(1,331 kg/ha).

• Journal of Forest and Environmental Science
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• v.38 no.4
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• pp.275-283
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• 2022

A study was designed to investigate the pattern of sexual dimorphism in a plantation of Garcinia kola. Twenty trees were randomly selected for the study and have been observed to flower regularly. A total of 100 inflorescence were randomly collected from the crown of each tree and 500 flowers randomly assessed within the period of four (4) flowering seasons. Floral sex assessment was done visually and with a hand magnifying lens; floral morphometric measurements (i.e. pedicel and perianth length and breadth), inflorescence length, and breadth) was taken using a veneer caliper; number of flowers per inflorescence and inflorescence per twig was counted; while, data analysis was conducted on excel using analysis of variance and pairwise t-test comparison. Four floral sexes were identified in the G. kola plantation studied which were unisexual male flowers, unisexual female flowers, cosexual unisexual male flowers, and cosexual hermaphrodite flowers. Three tree sexes were identified viz: inconstant male, invariant female, and cosexual trees. The plantation was significantly sexually dimorphic in floral sex and phenotypic traits (i.e. pedicel and perianth size), and as well as sexually dimorphic in tree sex and reproductive phenotypic traits (i.e. inflorescence size, number of inflorescences per twig, and number of flower bud per inflorescence). The sexual system of the plantation was therefore trioecious with features suggestive of evolving dioecy through the gynodioecious pathway.

• Journal of Korean Society of Forest Science
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• v.90 no.4
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• pp.558-564
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• 2001

For the study of morphological variation in winter buds of Q. variabilis $B_L$. natural populations in Korea, 16 populations were selected through the country in consideration of latitude, longitude, altitude, and geographical characters. Thirty trees were randomly selected from each population and 30 terminal and 30 lateral buds were sampled below 1/3 crown length of each tree. Four morphological characters including length and width of terminal and lateral buds were measured. 1. Length and width of terminal and lateral buds were in the ranges 6.9~11.3cm, 3.0~3.7cm, 6.1~8.9cm, and 2.5~3.1cm, respectively. The coefficient of variation were in about 20% in all the characters investigated. 2. All the characters were significantly different among populations as well as among individuals within populations. The degree of contribution of variance among individuals within populations was higher than that among populations. 3. Length of terminal bud showed positive correlation with length and width of lateral bud; and width of lateral bud with width of terminal bud and length of lateral bud. Also, positive correlations were observed between longitude and width of terminal bud, between latitude and length of terminal and lateral bud. 4. Cluster analysis using complete linkage method for winter bud characters showed two groups to Euclidean distance 3.4. They were group I of population 8 and group II of populations 1, 2, 3, 4, 5, 6, 7, 9, 10, 11, 12, 13, 14, 15, and 16. However, group II was divided into two at Euclidean distance 1.5 that are a group including populations 1, 2, 7, 9, and 11(groupII-1) and the other group including populations 3, 4, 5, 6, 10, 12, 13, 14, 15, and 16(groupII-2).