164 1. Introduction Persimmon trees, having no dwarf rootstocks of com- mercial value, tend to grow high. Lowering tree height by heavy dormant pruning has been a routine practice for efficient management of many persimmon orchards. In densely planted orchards, heavy pruning is an inevitable practice to restrict tree size. This practice, in turn, causes vigorous shoot growth resulting in an excessive crowding of the canopy. Poor fruit set and excessive supply of nitro- gen also stimulate the occurrence of vigorous shoots. Tree crowding not only hinders orchard operations, but dete- riorates fruit quality as the tree interior becomes heavily shaded. Shoots of vigorous and succulent growth make the tree susceptible to anthracnose (Colletorichum gloeospo- rioides) when humidity within the canopy is high. Summer pruning is one of many options to alleviate the problems of crowding, ensuring adequate light pen- etration into the canopy and controlling excessive shoot growth. However, removal of shoots during growing sea- son involves the loss of functional leaf surface, which may lead to reduced tree development and fruit growth. Loss of leaf area may also reduce reserve accumulation for early growth the next season. The effect of summer pruning on physiological process and tree growth seems well docu- mented in other deciduous fruit crops, but limited stud- ies have been conducted in persimmon. In this paper we evaluate the effects of summer pruning on tree growth, fruit quality, and nutrient composition of perennial organs in persimmon. 2. Tree response to summer pruning Vegetative growth Since removal of active leaf area reduces the produc- tion of dry matter during the growing season, summer pruning suppresses vegetative growth in other fruit crops, the effect of which is closely related to pruning severity, timing and cultivars (Taylor and Ferree, 1984; Rom and Ferree, 1985; Marini and Barden, 1987; Mediene et al., 2002; Zamani et al., 2006). In young ‘Fuyu’ and ‘Nishimu- rawase’ persimmons, thinning 26% of total shoot length in late July reduced dry weight of dormant one-year-old twigs, but it did not significantly affect total dry weights of aerial wood and the root (Choi et al., 2003 a). The result might be related in part to a high photosynthetic activity of remaining leaves until later in the season as shown in leaf chlorophyll concentrations (Fig. 1). Although not signifi- cant, negative relationships were observed between the in- crement of trunk cross-sectional area and pruning severity in the same experiment (Choi et al., 2003 a) and summer heading-back (Song et al., 2001). Summer pruning effect on tree growth and fruit production of persimmon S.T. Choi*, D.S. Park*, K.P. Hong*, S.M. Kang** * Sweet Persimmon Research Institute, Gyeongnam Agricultural Research and Extension Services, 262-1 Woodong, Jinyoung, Gimhae 621-802, Republic of Korea. ** Department of Horticulture, Institute of Agriculture and Life Science, Gyeongsang National Uni- versity, 900 Gazwa-dong, Jinju 660-701, Republic of Korea. Key words: pinching, secondary shoot, topping, tree vigor, water sprout. Abstract: This paper reviews the effect of summer pruning in persimmon (Diospyros kaki Thunb.) with regard to its posi- tive and negative aspects on tree growth and fruit production. In order for this practice to be of a significant value, a clear understanding is needed to appreciate the fact that so many variables are involved and much remains to be substantiated. Major reasons for summer pruning of persimmon are to improve fruit quality by enhancing light penetration into the tree canopy and to restrict vegetative shoot growth. Summer pruning generally suppresses tree growth even though it el- evates leaf activity. Positive effects of summer pruning on skin color, soluble solids, and appearance of fruits are observed mainly in those orchards where the trees are heavily dormant-pruned to lower tree height and to secure space in high density plantings. Secondary shoot pruning and topping could also improve fruit quality, increasing flower bud formation of remaining shoots. Summer-pruning effects are highly dependent on its severity and timing to affect tree growth, shoot regrowth, reserve accumulation, and fruit quality. Adv. Hort. Sci., 2011 25(3): 164-169 Received for publication 11 April 2011 Accepted for publication 13 May 2011 165 Leaf activity Summer pruning is known to increase photosynthe- sis, dark respiration, and transpiration of shoot leaves in other fruit crops (Taylor and Ferree, 1981; Marini and Barden, 1982; Myers and Ferree, 1983). As shoot thin- ning severity in late July increased in ‘Nishimurawase’ persimmon, specific leaf weight tended to become higher (Table 1). Chlorophyll content per unit area increased by 1.9-fold and 2.3-fold in ‘Fuyu’ and about 2-fold in ‘Nishimurawase’ trees that had been thinned 17% and 26% of their shoots, respectively (Fig. 1). Results indi- cated that photosynthesis can hardly compensate for the leaf area that has been removed, and there would be a sizable reduction in the production of photosynthates de- pending on pruning time Regrowth It is possible that shoot regrowth following summer pruning can have serious negative effects on the supply of photosynthates to fruit and shoot and resistance to dis- eases and pests (Forshey et al., 1992; Choi et al., 2003 b). In addition, excessive regrowth may reduce flower bud formation by gibberellins produced during shoot re- growth (Forshey et al., 1992). The extent of regrowth fol- lowing summer pruning was influenced by the time and severity (Miller, 1982; Ferree et al., 1984). When ‘Fuyu’ persimmon was summer-pruned on 20 June or 4 July, the earlier pruning produced more secondary growth more than the later one (Fujimura, 1932). Summer pruning af- ter late July, when buds enter physiological rest, did not result in a great problem of regrowth in persimmon trees, but heavy summer pruning may stimulate some buds to break into growth (Table 1). Heading-back cuts in vig- orous shoots would easily induce regrowth more than thinning cuts. Late July through early August is the ap- propriate time for thinning out vigorous shoots to avoid regrowth in South Korea. Reserve accumulation Early loss of foliage from pruning may result in reduced carbohydrate levels of the tree, and that could adversely af- fect cold hardiness (Marini and Barden, 1987). When the current shoots were thinned up to 26% of their total length in late July in young ‘Fuyu’ and ‘Nishimurawase’ persim- mon, the differences in non-structural carbohydrates and inorganic nutrients in four- to five-year-old wood of above- ground parts and the large root, measured on 2 April the fol- lowing year, were not consistent with the pruning severity the previous summer (Choi et al., 2003 a). This result might be due to the increased activity of the leaves as presented in chlorophyll concentration in figure 1. However, thinning 50% of total shoots decreased carbohydrate concentration in one-year-old shoots of field-grown ‘Nishimurawase’ (Ta- ble 2) but not in those of ‘Fuyu’ (Choi et al., 2003 b). In the same experiment, the severe summer pruning also reduced flower buds in both cultivars the following year, since low carbohydrates in the shoots (Choi et al., 2011) and exces- sive regrowth (Forshey et al., 1992) were negatively related to flower bud formation. 3. Fruit quality affected by summer pruning Summer pruning has been recommended to improve Table 1 - Effect of summer pruning severity on 29 July on light penetration and tree growth of ‘Nishimurawase’ persimmon (Choi et al., 2003 b) Shoot-thinned (%) Light penetration (%) TCSA increment (%) Regrowth (cm/tree) SLW (mg·cm-2) Leaf SPAD reading 0 11.3 b 6.8 a 0 a 10.14 b 51.6 a 25 24.7 a 7.8 a 63 a 10.92 ab 52.8 a 33 27.9 a 7.4 a 163 a 10.93 ab 51.8 a 50 30.9 a 6.1 a 215 a 11.18 a 54.8 a After summer pruning of seven-year-old trees, the leaf-fruit ratio was changed from 20 of 0% thinning to 10 of 50% thinning in an orchard planted at 3.5 x 2 m. TCSA= trunk cross-sectional area. SLW= specific leaf weight. Mean values in each column with the same letter are not significantly different by Duncan’s multiple range test at p≤ 0.05. Fig. 1 - Effect of different severities of shoot thinning on 22 July on leaf chlorophyll of five-year-old ‘Fuyu’ and ‘Nishimurawase’ persimmon on 3 November. Chlorophyll content includes chlo- rophylls a and b. Values sharing the same letter are not signifi- cantly different from each other by Duncan’s multiple range test at p≤ 0.05 (Choi et al., 2003 a). µ g 166 fruit quality in vigorous persimmon by increasing light interception (Mowat, 1987; Ullio, 2003; George et al., 2005; Yamada, 2008). However, there was no consistent effect of the pruning on fruit characteristics in many stud- ies. Table 3 shows that thinning out some water sprouts in late July increased skin color with no reduction in fruit size. This kind of positive result might be possible in vigorous ‘Fuyu’ trees in densely-planted orchards, and the leaf-fruit ratio after the pruning was sufficiently high. Kim (2010) also found larger size and higher coloration of fruits in vigorous ‘Fuyu’ trees after thinning out some water sprouts in late July. Lower water consumption and thus improved water status during the growing season af- ter summer pruning could benefit fruit growth and relieve the potential detriment due to carbohydrate shortage in apple (Li et al., 2003) and peach (Lopez et al., 2006). Fruit firmness was not significantly changed by the differences in pruning severity (Tables 4 and 5). Size, soluble solids, and skin color of persimmon fruits decreased when the leaf-fruit ratio was low (Choi et al., 2010). The appropriate leaf-fruit ratio for quality ‘Fuyu’ fruits has been set at about 20 in Korea (Choi et al., 2010) and Japan (Kishimoto, 1975; Yamamura et al., 1989). Loss of leaf area by summer pruning results in poor fruit quality Table 3 - Effect of removing water sprouts on 28 July on light penetra- tion and fruit characteristics in vigorous ‘Fuyu’ persimmon orchard (Choi et al., 2005) Treatment Light penetration (%) Fruits Average weight (g) Skin color (Hunter a) Soluble solids (°Brix) Non-pruning 15 243 27.9 15.0 Summer pruning 33 257 29.8 15.2 Significance ** ns * ns By summer pruning of 1-year-old trees, water sprouts were removed to maintain leaf-fruit ratio 20 in an orchard planted at 6 x 3 m. ns= not significant; * = significant at P≤ 0.05; ** = significant at P≤0.01. Table 4 - Effect of summer pruning severity on 28 July on fruit characteristics of ‘Fuyu’ persimmon harvested on 31 October (Choi et al., 2003 b) Shoot-thinned (%) Average weight (g) Skin color (Hunter a) Fruit firmness (N) Soluble solids (°Brix) Skin damage (%) 0 234 a 27.6 a 20.7 a 15.2 a 13.2 a 10 244 a 28.4 a 21.9 a 15.7 a 9.3 cb 20 249 a 28.3 a 20.1 a 15.1 a 7.8 c 30 233 a 29.5 a 20.3 a 15.3 a 9.8 b After summer pruning of seven-year-old trees, the leaf-fruit ratio was changed from 39 of 0% thinning to 28 of 30% thinning in an orchard planted at 6 x 3 m. Skin damage: blemish or stains on fruit skin. Mean values in each column with the same letter are not significantly different by Duncan’s multiple range test at P≤0.05. Table 5 - Effect of summer pruning severity on 29 July on fruit characteristics of ‘Nishimurawase’ persimmon harvested on 26 September (Choi et al., 2003 b) Shoot-thinned (%) Average weight (g) Skin color (Hunter a) Fruit firmness (N) Soluble solids (°Brix) Skin damage (%) 0 144 a 32.2 a 34.3 a 14.5 a 8.8 a 25 139 a 32.2 a 33.4 a 14.0 ab 3.7 ab 33 137 a 31.2 ab 32.5 a 13.6 ab 4.6 ab 50 141 a 27.7 a 31.9 a 13.0 b 1.6 b After summer pruning of seven-year-old trees on 29 July, the leaf-fruit ratio was changed from 20 of 0% thinning to 10 of 50% thinning in an or- chard planted at 3.5 x 2 m. Skin damage: blemish or stains on fruit skin. Mean values in each column with the same letter are not significantly different by Duncan’s multiple range test at p≤0.05. Table 2 - Effect of summer pruning severity on 29 July on concentrations of carbohydrates and inorganic elements in dormant shoots of ‘Nishimu- rawase’ persimmon on 17 February (Choi et al., 2003 b) Shoot-thinned (%) Carbohydrates (% DW) Inorganic elements (% DW) Soluble sugars Starch N P K Ca Mg 0 12.2 a 5.4 a 0.60 a 0.21 b 0.60 a 0.36 b 0.17 a 25 12.0 a 4.4 ab 0.62 a 0.24 ab 0.73 a 0.39 ab 0.17 a 33 10.3 a 3.5 ab 0.60 a 0.24 ab 0.74 a 0.43 a 0.17 a 50 9.7 a 3.2 b 0.62 a 0.28 a 0.75 a 0.44 a 0.18 a After summer pruning of seven-year-old trees, the leaf-fruit ratio was changed from 20 of 0% thinning to 10 of 50% thinning in an orchard planted at 3.5 x 2 m. Mean values in each column with the same letter are not significantly different by Duncan’s multiple range test at p≤ 0.05. 167 if the pruning significantly reduces the ratio. When leaf- fruit ratio decreased to less than 13 with severe removal of the shoots, fruit size, skin color or soluble solids were significantly reduced (Table 5) (Choi et al., 2003 a). On the other hand, strong winds result in blemish of fruit skin due to rubbing of shoots and leaves against fruits (George et al., 1997 a). Skin staining of persimmon fruits is of- ten caused by humid conditions in autumn (George et al., 1997 a), which become aggravated by the shoots growing vigorously. Thinning out some of the shoots in summer reduces these damages by improving the micro-environ- ment within the tree canopy (Tables 4 and 5). Therefore, summer pruning has been recommended as a means to re- duce the occurrence of skin staining (George et al., 1997 a, 2005), especially in newly-released Japanese cultivars like a crack-susceptible ‘Taishu’ (Yakushiji and Nakat- suka, 2007). The influence of summer pruning on fruit quality varies by the degree of canopy crowding and the timing and its severity, as has been documented in other fruit crops (Marini and Barden, 1987; Forshey et al., 1992; Zamani et al., 2006). 4. Water sprout management Removing all water sprouts of vigorous trees too ear- ly in the season may induce severe regrowth (Fujimura, 1932), which disturbs light penetration and reserve ac- cumulation in perennial organs (Kappel et al., 1983). Therefore, instead of removing all water sprouts, thinning some of them combined with bending or twisting the re- maining ones down to horizontal in June may be recom- mended (Park and Choi, 2000; Huh et al., 2003; George et al., 2005). Securing leaf area even in water sprouts helps prevent the regrowth that may be related to the action of hormones produced in old leaves (Forshey et al., 1992). Some of the water sprouts may have some value as mother branches the next season. Water sprouts of ‘Fuyu’ could form flower buds as long as their terminal buds are set by early August in South Korea (Choi et al., 2011): they could serve as fruiting branches for the following year. In vigorous trees with poor fruiting, using the sprouts as mother branches to set fruits the next season is extremely important to make up for the yield reduction as well as to control tree vigor. When the sprouts were twisted and bent down under horizontal in mid- to late June after thin- ning out some, flower buds were formed in 84 to 97% of them the following year (Park and Choi, 2000). Changes in endogenous hormones might be closely involved in this treatment, particularly low gibberellin and high cytokinin, which play a role in flower bud formation (Banno et al., 1985). Heading-back pruning to four buds is also practiced in New Zealand to ensure future fruiting site from water sprouts (Mowat, 1987). 5. Secondary-shoot pruning, pinching and topping Secondary growth from shoot terminal occurs from mid-June in vigorous persimmon trees (Nii, 1980; Park et al., 2003). Secondary growth often induced fruit drop (George et al., 1997 b). Park et al. (2003) studied the head- ing-back effect of secondary shoots leaving two to three basal leaves of the secondary growth on ‘Fuyu’ persim- mon. When the heading-back was done on fruiting shoot, they found that the shoots had a lower dry weight which was accompanied by an increase in fruit weight. The re- sult indicated the necessity of such cuts for fruit growth. Compared with the heading-backs before 10 July or after 10 August, those on 25 July produced the largest fruits in- season and exhibited the highest percentage of shoots that bore flowers and fruits the following year, indicating that pruning the secondary shoots on 25 July helps to direct the assimilates to fruit growth and flower bud development, not to vegetative growth. ‘Nishimurawase’ persimmons tend to bear staminate, not pistillate, flowers when the trees are old and not vigor- ous enough. Chijiwa and Hayashi (2007) reported a way to use water shoots to serve as fruiting mother branches for the next season by pinching at 15 cm from the base between May and June. Shoots left after the pinching or summer shoots regrown from the cut bore more pistil- late and fewer staminate flowers the following year than the un-treated water shoots. Takano (1994) also reported a better mother branch formation by pinching adventi- tious buds of persimmon. The size of trees and yield ef- ficiency are among the most important considerations in high density orchards. When the vigorous shoots of young ‘Uenishiwase’ persimmon were topped to a 30- cm length in early June, followed by the removal of the regrowth, trunk growth decreased and fruit set increased the following year (Song et al., 2001). The occurrence of secondary growth after heading was dependent on the treatment date. Topping the shoots at the fourth bud from the terminal on 20 May promoted secondary growth of ‘Hiratanenashi’ persimmon, but the same treatment after 22 June did not (Hasegawa and Nakajima, 1984). The summer topping of long shoots in summer was effec- tive in forming fruiting shoots the following year in their lower parts. Pinching and topping the shoot would pro- mote flower bud formation of that shoot if regrowth is not severe. 6. Conclusions Severe summer pruning could suppress vegetative and fruit growth due to the lowered photosynthetic capacity, reducing the carbohydrate reserves in persimmon tree. However, summer pruning which is appropriate to tree vigor and environmental conditions would increase pro- duction of quality fruits by improving light distribution in the tree canopy or restricting vegetative growth. Since tree vigor is a result of the complex interactive effects with cultural practices, the pruning alone should not be used as a tool for controlling vegetative growth. It is necessary to incorporate the pruning into a comprehensive program 168 such as tree training, fruiting, irrigation, and fertilization to reduce vigorous growth. Growers should employ sum- mer pruning methods while carefully monitoring for po- tentially negative effects on tree growth and fruit quality. References BANNO K., HAYASHI S., TANABE K., 1985 - Effects of SADH and shoot-bending on flower bud formation, nutrient components and endogenous growth regulators in Japanese pear (Pyrus serotina Rehd.). - J. Japan. Soc. Hort. Sci., 53: 365-376. CHIJIWA H., HAYASHI K., 2007 - The formation of fruiting mother shoot from water shoot by pinching in Japanese per- simmon. - Hort. Res., 6: 265-270. CHOI S.T., KANG S.M., PARK D.S., SONG W.D., AHN G.H., 2003 a - Effect of different severities of summer pruning on fruit characteristics and tree growth in young ‘Fuyu’ and ‘Nishimurawase’ persimmon. - J. Korean Soc. Hort. Sci., 44: 569-574. CHOI S.T., PARK D.S., AHN G.H., 2003 b - Studies on efficient production and quality improvement of sweet persimmon - Effect of summer pruning on fruit qualities of sweet persim- mon. - Rural Development Administration Report. Suwon, Korea, pp. 5-34. (in Korean with English summary). CHOI S.T., PARK D.S., KANG S.M., 2011 - Nutrient accumu- lation and flower bud formation affected by the time of ter- minal bud set on water sprouts of persimmon. - HortScience, 46: 523-526. CHOI S.T., PARK D.S., KANG S.M., CHO Y.C., 2010 - Effect of fruit-load on the growth, absorption, and partitioning of inorganic nutrients in young ‘Fuyu’ persimmon trees. - Sci. Hort., 126: 408-412. CHOI S.T., PARK D.S., KIM S.C., 2005 - Summer pruning and management for vigorous persimmon trees. - 2005 Farming technology. Rural Development Administration. Suwon, Ko- rea. (in Korean) FERREE D.C., MYERS S.C., ROM C.R., TAYLOR B.H., 1984 - Physiological aspects of summer pruning. - Acta Horticul- turae, 146: 243-252. FORSHEY C.G., ELFVING D.C., STEBBINS R.S., 1992 - Training and pruning apple and pear trees. - Amer. Soc. Hort. Sci., pp. 60-63. FUJIMURA J., 1932 - Effects of summer pruning on the second- ary growth of one-year-old persimmon and Japanese pear trees. - J. Japan. Soc. Hort. Sci., 3: 9-20. GEORGE A.P., MOWAT A.D., COLLINS R.J., 1997 a - Factors affecting blemishing of persimmon in New Zealand and Aus- tralia. - Acta Horticulturae, 436: 171-178. GEORGE A.P., MOWAT A.D., COLLINS R.J., MORLEY- BUNKER M., 1997 b - The pattern and control of repro- ductive development in non-astringent persimmon (Dios- pyros kaki L.): a review. - Sci. Hort., 70: 93-122. GEORGE A.P., NISSEN B., BROADLEY R., COLLINS R.J., RIGDEN P., JEFFERS S., ISAACSON B., LEDGER S., 2005 - Sweet persimmons grower’s handbook. - Department of Primary Industries and Fisheries, Brisbane, Queensland, Australia. HASEGAWA K., NAKAJIMA Y., 1984 - Effects of topping on the growth and fruit quality of the Japanese persimmon. - Res. Rpt. Kochi Univ. (Agr.), 33: 43-53. HUH M.S., SONG I.K., CHO D.H., JEONG Y.S., 2003 - Bend- ing effect of vigorous shoot on persimmon tree. - 2003 Annu- al Research Report. Gyeongsangbuk-do Agr. Res. Ext. Serv. Daegu, Korea. (in Korean) KAPPEL F., FLORE J.A., LAYNE R.E.C., 1983 - Character- ization of the light microclimate in four peach hedgerow canopies. - J. Amer. Soc. Hort. Sci., 108: 102-105. KIM B.S., 2010 - Development of cultivation techniques for the stable production of high quality sweet persimmon fruits to export - A study on quality enhancement of sweet persimmon for export by stable tree vigor. - Rural Development Admin- istration, Suwon, Korea. (in Korean). KISHIMOTO O., 1975 - Estimations of optimum range of de- gree of fruit thinning and desirable fruit weight in Japanese pears and persimmon tree. - J. Japan. Soc. Hort. Sci., 43: 368-376. LI K., LAKSO A.N., PICCIONI R., ROBINSON T., 2003 - Sum- mer pruning reduces whole-canopy carbon fixation and tran- spiration in apple trees. - J. Hort. Sci. Biotechol., 78: 749-754. LOPEZ G., MATA M., ARBONES A., SOLANS J.R., GIRO- NA J., MARSAL J., 2006 - Mitigation of effects of extreme drought during stage III of peach fruit development by sum- mer pruning and fruit thinning. - Tree Physiol., 26: 469-477. MARINI R.P., BARDEN J.A., 1982 - Net photosynthesis, dark respiration, transpiration, and stomatal resistance of young and mature apple trees as influenced by summer or dormant pruning. - J. Amer. Soc. Hort. Sci., 107: 170-174. MARINI R.P., BARDEN J.A., 1987 - Summer pruning of apple and peach trees. - Hort. Rev., 9: 351-375. MEDIENE S., JORDAN M.O., PAGÈS L., LEBOT J., AD- AMOWICZ S., 2002 - The influence of severe shoot pruning on growth, carbon and nitrogen status in young peach trees (Prunus persica). - Tree Physiol., 22: 1289-1296. MILLER S.S., 1982 - Regrowth, flowering, and fruit quality of ‘Delicious’ apple trees as influenced by summer pruning. - J. Amer. Soc. Hort. Sci., 107: 975-978. MOWAT A., 1987 - Pruning persimmons. - HortResearch publi- cation. New Zealand. March 28, 2011. - http://www.hortnet. co.nz/publications/science. MYERS S.C., FERREE D.C., 1983 - Influence of summer prun- ing and tree orientation on net photosynthesis, transpiration, shoot growth, and dry-weight distribution in young apple trees. - J. Amer. Soc. Hort. Sci., 108: 4-9. NII N., 1980 - Current shoot and growth in Japanese persim- mon, Diospyros kaki cv. Fuyu, in relation to the development of the tissue system in the leaf. - J. Japan. Soc. Hort. Sci., 49: 149-159. PARK D.S., CHOI S.T., 2000 - Development of technology for production of high quality fruits in sweet persimmon - Stud- ies on the method of fruit-load adjustment for high quality of fruit production. - Rural Development Administration Re- port, Suwon, Korea. (in Korean with English summary). PARK D.S., KANG S.M., CHOI S.T., LIM C.A., SONG W.D., 2003 - Effect of secondary-shoot prunings on fruit growth and following year’s fruit set of ‘Fuyu’ persimmon. - J. Ko- rean Soc. Hort. Sci., 44: 678-682. ROM C.R., FERREE D.C., 1985 - Time and severity of summer pruning influences on young peach tree net photosynthesis, 169 transpiration, and dry weight distribution. - J. Amer. Soc. Hort. Sci., 110: 455-461. SONG W.D., CHOI S.T., KIM S.C., PARK D.S., KANG S.M., 2001 - Effect of pinching on fruit set of young sweet per- simmon trees during the following years. - 2001 Annual Research Report. Gyeongsangnam-do Agr. Res. Ext. Serv. Jinju, Korea. (in Korean) TAKANO S., 1994 - Better branch formation by pinching ad- ventive buds of Japanese persimmon. - Bull. Nara Agr. Expt. Sta. J., 25: 36-37. TAYLOR B.H., FERREE D.C., 1981 - The influence of summer pruning on photosynthesis, transpiration, leaf abscission, and dry weight accumulation of young apple trees. - J. Amer. Soc. Hort. Sci., 106: 389-393. TAYLOR B.H., FERREE D.C., 1984 - The influence of summer pruning and cropping on growth and fruiting of apple. - J. Amer. Hort. Sci., 109: 19-24. ULLIO L., 2003 - Persimmon growing in New South Wales. - Agfact H3.1.17, 3rd edition. Elizabeth Macarthur Agricul- tural Research Institute, Camden, Australia. YAKUSHIJI H., NAKATSUKA A., 2007 - Recent persimmon research in Japan. - Japan. J. Plant Sci., 1(2): 42-62. YAMADA M., 2008 - Persimmon propagation, orchard plant- ing, training and pruning in Japan. - Adv. Hort. Sci., 22: 269-273. YAMAMURA H., MATSUI K., MATSUMOTO T., 1989 - Ef- fects of gibberellins on fruit set and flower-bud formation in unpollinated persimmon (Diospyros kaki). - HortScience, 38: 77-86. ZAMANI Z., SAIE A., TALAIE A.-R., FATAHI R., 2006 - Ef- fects of summer pruning on growth indices of two important Iranian apple cultivars ‘Golab’ and ‘Shafi-Abadi’. - Acta Horticulturae, 707: 269-274.