28 research outputs found
Seasonal changes in respiratory rates of cultivated cuttings of Cryptomeria japonica after root initiation (Forestry)
åŒåžéãç¥ãããã§åºç€çãªè³æãšãªãåŒåžé床(mgCO_2/g dry weight/hour at 25â)ã, ã¹ã®ã®ããæšèãçšããŠ, çºæ ¹çŽåŸããçŽ2幎éã«ããã, 1ãµæééã§ããšããã枬å®ã¯åäœãšéšå(0幎ç, 1幎ç, 2幎çã®åè, 䞻軞, å°äžäž»è»ž, æ ¹)ã«ãããŠè¡ãªã£ããåŒåžé床ã¯åäœ, åéšåã®ãããã«ã€ããŠã, æ¥ãšç§ã«æ¥æ¿ã«å¢å ã, æ¥ããå€, ç§ããå¬ã«ãããŠç·©æ
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ã§ã®æµããèãããããThe respiratory rates (mgCO_2/g dry weight/hour at 25â) are used as data when we estimate the amount of respiration. In this experiment, the respiratory rates of cuttings of Cryptomeria japonica were measured at intervals of one month during about two years from immediately after root initiation. The rates of individual and six sections, such as zero year old leaf, one year old leaf, two years old leaf, terrestrial-stem, subterranean-stem (inserted stem under the ground for cutting) and root were measured. The respiratory rates, in both case of individual and sections, showed the tendencies to increase rapidly in spring and fall, and to decrease gradually from spring to summer and from fall to winter (see Figure 1,2 and 5.), too. However only the rates of root somewhat differed from these tendencies, its respiratory rates showed the tendencies to increase also in winter and to increase regularly at intervals of five months (see Figure 6.). It is considered that these seasonal changes in respiratory rates were influenced considerably by the rise and fall of periodic physiological activity, seeing that growing season of Cryptomeria japonica exists in spring and fall. And it is supposed as one reason that the rates of fall observed relatively high values were affected by the strong irradiation of sunlight because sun-shade was taken off September. The respiratory rates of leaf decreased with the lapse of time, namely, with the lapse of leaf-age. For this reason, it is estimated that physiological activity of leaf falls every year. When leaf passes for four to five years in the future, it is supposed that the rates of leaf do not depend on seasonal periodicity, and leaves live only basic metabolism at various temperatures, or defoliate. It is considered that the gradual decrement in respiratory rates from fall to winter depends on the temperature, on the other hand, the gradual decrement from spring to summer is due to a series of dry matter production without accompanied by respiratory substances. Because, when dry matter production continues without accompanied by increment of respiratory substances, or respiratory activity, if the respiratory rates are given by \u27per unit dry matter weight\u27, then the rates are indicated necessarily by the tendency of decrement. But it is supposed that just before beginning of growth, respiratory substances are increased and activated by the changes and the translocations of material, seeing that the rates increase rapidly in spring and fall. And if the respiratory rates are compared leaf and terrestrial-stem (above the ground) with subterranean-stem and root (under the ground), then it is recognized that the seasonal changes in the respiratory rates are slightly different. Therefore, it is estimated that respiratory substances translocate the interior of plant. The respiratory rates of individual and those of total section did not agree. The rates of total section were extremely high values than those of individual. It is considered that in each section, large amounts of CO_2 were released by the excision of plant organs
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暹霢100∿150幎çã®ã³ãã©æçæã«ãããŠ1982,83幎ã®ç¹æ®åšå®åéšã®çç£éã枬å®ã, èå¯ããããã®æåæé¢ã¯ååãã§æ¥åŸæ(å¹³å34床)ã§ãããè±ç²ä»¥å€ã®åéšçç£éã¯ãªã¿ãŒãã©ããæ³ã«ãã, è±ç²ã¯éããåã®éè±åºã«ã€ãè±ç²é調æ»ã䜵çšã, 也éãšåæ°ã«ã€ããŠæšå®ããã也ç©çç£éã¯1982幎ã300kg/haã»y, 1983幎750kg/haã»yã§, éæ§ãéæ§ã®éšåã1983幎ã®æ¹ãå€ã, ãšãã«çš®åã®å¢å ãèããã£ããè±äœå¹Žã«ã¯ä¹Ÿç©çç£éå
šäœã«å ããéæ§éšåã®å²åãé«ã(55%), å¶äœå¹Žã«ã¯äœãã£ã(20%)ã1983幎ã®çš®åè±äœã¯éè±ãããè±æ°ãå¢å ããããš(2.6å)ãšçµå®çãé«ãã£ãããš(2åå¢å )ã«ããããã£ãããã®çµå®çã®å¢å€§ã¯è±ç²ç²ã®çç£åæ°ã®ãã(1.2Ã(10)^⇾1.6Ã(10)^no./haã»y)ã«å¯Ÿå¿ããŠãããäžæ¹, ãè±æ°ã«å¯Ÿããè±ç²ç²æ°ã®æ¯ã«ã¯äž¡å¹ŽåºŠã®éãã¯å°ãã, ããã¯ã¹ã®, ããã, ãªãã°ã«ãã®æåã§èªããããŠããçµæãšäžèŽãããAnnual production rates (by dry weight and number) of each component of reproductive organs in a Konara oak (Quercus serrata THUNB.) mature stand, which consisted of trees 100-150 years old, were measured in 1982 and 1983 and analyzed. The slope of the studied stand faced south and was steep (mean inclination : 34°). Production rates per 1-ha stand for each component except pollen were determined using ten litter traps (each measuring 0.5Ã0.5m), while for pollen, this was done together with measurement of the amount of pollen contained in catkin samples before anther opening. The dry matter production rate of all reproductive parts including pollen in 1982 and 1983 amounted to 300 and 750kg/haã»y, respectively; the increase in 1983 was recognized in both male and female parts, especially acorns. In abundant crops the proportion of female parts to the total production was high (50%), while in poor crops, the proportion was low (20%). The higher production of acorns in 1983 compared with 1982 was caused by an increase in both the potential number of female flowers (2.6 times) and the ratio of fruits which matured (2 times). Changes in the seed-maturing ratio, i.e., the proportion of female flowers developing into mature and sound acorns, was related to the pollen production rate, which varied from 1.2Ã(10)^ to 1.6Ã(10)^ grains/haã»y. Little difference between the two years in the ratio of the number of pollen grains to female flowers was found, which agreed with our previous findings for Sugi (Cryptomeria japonica), Hinoki (Chamaecyparis obtusa) and Siebold walnut (Juglans ailanthifolia) stand
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ã®ã·ã€æçæã«ãããŠ, ãªã¿ãŒãã©ããæ³ã§1986幎∿1989幎ã®çæ®åšå®ã®çç£é(æååœãã)ã枬ã, ãŸãè±ç²çç£éã¯éè±åã®éè±åºåœããè±ç²éãåºã«æšå®ããããããã®è«žéãæ€èšã, ææ§çæ®ã«ã€ããŠããäž»ãªçµæã¯æ¬¡ã®éãã§ãããè±ç²çç£éã¯éé(218∿359kg (ha)^ (yr)^)ã§ã¯æ倧ã¯ã©ã¹, ç²æ°(64.2∿103Ã(10)^(ha)^ (yr)^)ã§ã¯çªåºããŠå€ã, ããã幎次å€åãå°ããã£ãããã®è«å€§ãªè±ç²æ°ã¯, ããã, èç æ°ã«èŠåã£ããã®ã§ãã£ã(è±ç²/èç ã®æ°æ¯, 4.1∿8.3Ã(10)^5)ãè±ç²ç²ã¯å°åœ¢ã§ãããã(1.94∿4.30Ã(10)^mg), ååç£ç©ã®è±ç²ãžã®æµãã¯ç¯çŽãããŠãããéè±å¹Žããšã®ä¹Ÿç©éã¯1609∿1803kg (ha)^ã§, éæ§ãšéæ§ã®éšåéã¯éæ¯äŸã®é¢ä¿ã«ãã£ãã幎床ããšã®ä¹Ÿç©çç£éã¯1237∿2204kg (ha)^ (yr)^ã®ç¯å²ã§, ããã¯çš®åã®äžŠäœ∿å¶äœã®å¹Žã®å€ã§ããããã®çç£éã®å€å°ãšåéšåã®å²åãšã®éã«ã¯, äžå®ã®åŸåã¯ãªãã£ããããã¯çš®åæçã«2ã«å¹ŽãèŠããããšã«é¢ä¿ãããããŸã, åœå¹Žçãš1幎çã®éšåã®çç£éã¯çãããªã幎ãå€ãã£ããçµå®çã¯äœãã(5.5%∿10.6%), ã»ãã®çš®ãšå€§ç¥çããã幎ã
ã®çš®åæ°ã¯çµå®çãšäžŠè¡ããŠæšç§»ã, ç·éè±æ°ãçš®åçç£ã«é¢ä¿ãããããã ãçš®å察æè³ã®ééæ¯ã¯çš®åã®äžŠäœå¹Žã«3å, å¶äœå¹Ž6åã§, ããã¯ã»ãã®éåæ£åžçš®åã®çš®ã®å€ãšäžèŽãããIn a mature stand of Shii chinkapin (Castanopsis cuspidata SCHOTTKY) at Matsuotaisya shrine, Arashiyama, Kyoto, annual production rates of reproductive organs were studied using 20 litter traps (each 50cmÃ50cm in mouth area) in 1986-1989,and those of pollen were estimated by multiplying the number of fallen male catkins per ha per year by the mean amount of pollen per catkin before anthesis. The main results were as follows. The pollen production rate of 218-359kg d. w. (ha)^ (yr)^ was one of the highest among other species, and that of 64.2-103Ã(10)^(ha)^ (yr)^ was by far the largest number; moreover, these showed small year-to-year fluctuations. Such a huge number of pollen grains, however, was balanced by the number of ovules in a stand (numerical ratio of pollen grains to ovules : 4.1-8.3Ã(10)^5). The light pollen grains (1.94-4.30Ã(10)^mg d. w.) save the assimilation products invested in pollen formation. Dry matter of reproductive organs by the year of anthesis was within the range 1609-1803kg d. w. (ha)^, and those of male and female parts were inversely proportional to each other. Annual production rates were within the range 1237-2204kg d. w. (ha)^ (yr)^, equivalent to values in years of average to poor seed crop. There was no relationship between the annual production rates (by weight) of male and female parts, because fruit maturation requires two growing seasons. In three years among four, the 0-and 1-yr-old parts showed equal dry weight allocation. Seedmaturing ratios or numerical ratios of mature nuts to total female flowers were small (5.5%-10.6%), being approximately equal to those of other species. The year-to-year trend in nut production (by number) parallelled those of seed-maturing ratio and the number of female flowers. Mean nut weight vs. assimilation products necessary for producing a single nut, calculated by dividing the drymatter production rate of overall parts by the number of nuts, was 1 : 3 in a year with an average seed crop, and 1 : 6 in a year with a poor crop. This seed production effort was similar to those of five other barachorous species
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æå1haãããã®éè±åº, è±ç², éè±åã³çš®åã®çç£é(也éãšåæ°)ã«ã€ããŠ, è霢ããºãã©æåã®æ±åãæé¢ãšè¥¿åãæé¢ãšãæ¯èŒæ€èšã, çš®åçç£ã«é¢ä¿ããèŠå ãèå¯ãããåéšåã®çç£éã¯ãã©ããæ³ã§æž¬å®ã, è±ç²ã«ã€ããŠã¯éè±åã®éè±åºè©Šæã«å«ãŸããè±ç²éãšæåã®éè±éè±åºæ°ããããŠæšå®ããã調æ»ã¯1984幎ãš85幎ã«è¡ã£ãã䞡幎床ã¯çš®åè±äœå¹Žãšå€æãããäž¡æåã®2幎éã®ä¹Ÿç©çç£ã¯450∿500kg/haã»yrã§, ããã«å ããéæ§éšåã®å²åã¯æ±åãæåã1/4,西åãæåã¯1/8ã§ãã£ããçš®åçç£ã¯è¥¿åãæåã®æ¹ãå€ã, ããã¯éè±æ°ãå€ãããã§ãã£ããçš®åçç£ã®å¹Žå€åã¯çµå®çã«æ¯é
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ãããšããããè±ç²/çš®åã®æ°æ¯ã¯, çš®åçç£ã®å°ãæ±åãæå(19Ã(10)^6å)ã®æ¹ã西åãæå(5∿6Ã(10)^6å)ãã4åçšåºŠå€ãã, äž¡æåã®çµå®çã¯çããã£ãããã®ããã«, åããåã£ãŠæ¥ããæ±åãåã³è¥¿åãæåã«ãããéæ§ãšéæ§éšåã®çç£éåã³äž¡è
ã®äž¡å²åã¯ç°ãããšãããã£ããA comparison of east- and west-facing slopes with regard to the production rates of male flowers, pollen, female flowers and seeds in aged stands of Japanese white oak (Quercus mongolica FISCH. var. grosseserrata REHD. et WILS.) was made and the factors affecting seed production were discussed. Annual production rates (by dry weight and number) per 1-ha stand for each reproductive component except pollen were determined using ten litter traps (each 50cmÃ50cm in mouth area), while for pollen, this was done together with measurement of the amount of pollen contained in catkin samples before anther opening. The study was conducted in 1984 and 1985,years in which the seed crop was abundant. Dry-matter production rates for all reproductive parts including pollen in the two stands for the two study years were in the range of 450∿500kg/haã»yr, the proportion of male parts being one-fourth for the east-facing stand and one-eighth for the west-facing one. Seed production of the west-facing stand was higher than that of the east-facing one, due to the number of female flowers. Yearly changes in seed production were dependent on the seed-maturing ratio, i.e., the numerical ratio of sound acorns to female flowers, and not on the number of female flowers. The high seed-maturing ratio corresponded to the year in which a large amount of pollen was available for fertilization. Judging from the negligible difference between the two years in the numerical ratio of pollen to seeds, i.e., the number of pollen grains necessary for the formation of one acorn, seed production appears to be dependent on the number of pollen grains released into the air. There were no differences between the two stands in the seed-maturing ratio, while the numerical ratio of pollen to seeds in the east-facing stand (19Ã(10)^6), which had a low seed production, was about four times higher than that in the west-facing stand (5-6Ã(10)^6). Remarkable differences between the two stands, either neighboring or face to face, were found in the numerical proportion of male to female parts
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京éœçå°ããšããŸãäœå±±åž¯ã®ã·ã€5æåã察象ã«ããŠ1982,83幎ã®æåãããéè±, è±ç², æå®ã®çç£é(也éãšåæ°)ããã©ããæ³ã§èª¿æ»ã, éè±∿çš®åæ£åžã®éçšã解æãããè±ç²çç£éã¯æ¢å ±4暹皮ããå€ã, ç²æ°ã§ã¯2.6Ã(10)^ha^y^ãèšé²ãããéè±ã®çç£éã¯æåã®çè²æ®µéã®é²è¡ã«äŒŽãå¢å ããã, æå®ã«ã¯ãã®åŸåãèªããããªããçæ®åšå®å
šäœã®çç£éã¯10è³æã®ãã¹ãŠã1t ha^y^ããã, ãã¡3æåã¯3∿5.5t ha^y^ã«éããã1982幎éè±ã«ç±æ¥ããçæ®åšå®éšåã®ä¹Ÿç©å²åã¯éæ§ : éæ§ã1 : 1ã®3æåãš1 : 3ã®2æåã«ããã, ãã®é¢ä¿ã¯è±ç²ç²æ°P/ãè±æ°Fã®æ¯ã«ãã£ãŠæŽçã§ãããåè
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2æåã§ã¯çµå®çãé«ãæå(31%)ãšäœããã®(17%)ãšããã£ããè¥ãæåã§ã¯P/Fæ¯ãå°ããã, çµå®çã¯é«ãåŸåãã¿ããããã·ã€çš®åçç£ã決å®ããèŠå ã«ã¯ãè±æ°ãšçµå®çã®äºã€ãèªãããããAnnual production rates (per 1-ha stand; by dry weight and number) of catkins, pollen and fruits of five chinkapin (Castanopsis cuspidata SCHOTTKY) stands in the mountain zone around the Koyto Basin were measured in 1982 and 1983 using litter traps, and analyzed from the process of flowering to seed dispersal. The pollen production rates were larger than those of the four species previously reported, i.e., Japanese red pine, Cryptomeria, Chamaecyparis and Siebold walnut; the maximum value reached 2.4Ã(10)^ grains/haã»y. Catkin production increased with developing growth stage of stands, while fruit production varied among stands. Ten estimations (five stands in two years) of the production rates of all reproductive organs including pollen showed values of over 1t/haã»y, in which all six estimations for three stands amounted to between 3 and 5.5t/haã»y. The distribution ratio of male and female organs within the total dry matter production of parts derived from flowering in 1982 was 1 : 1 for three Stands B, D and E, and 1 : 3 for two Stands A and C, corresponding to the ratio of the number of pollen grains (P) to female flowers (F). In the former stands, a two-fold difference in the numbers of female flowers was recognized, while there was no difference in the seed-maturing ratio (21%), i.e., the proportion of female flowers developing into ripe and sound nuts. Of the latter stands having half the P/F Ratio of the former, young Stand A showed a high ratio (31%) while Stand C showed a low ratio (17%). It was concluded that the seed-maturing ratios in mature stands are related to the P/F Ratio, while in young stands, the former tends to be high in spite of a low P/F Ratio
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空éã®æ¯æãæ¯æšéããã³A_0å±€ã®ææ©ç©éã¯å€ããŠç©è³ªåŸªç°ã¯æªãã£ããã»ãã®æž¬å®éãçç£æ§é ã¯äººå·¥æã®ç¯å²å
ã«ãã£ãŠ, 貧匱ãªèª¿æ»æã®ç¹åŸŽã¯ãšãã«èªããããªãã£ãããããæã®èª¿æ»å ±åãšæ¯èŒæ€èšãããšãã, å¬å£ã®æåèé10t/haãééãããããæã®äžéã§ããããšãããã£ãããŸãå°äžéšçŽçç£é床7.77t/haã»yããããæã®äžéãšã¿ãã, ããã¯æé·è¯å¥œãªäººå·¥æã®çŽ50%ã«ããã£ããEstimates were made of the aboveground biomass, litterfall rate and net production rate for the natural regenerated forest of Chamaecyparis obtusa S. et Z. growing on the poor site. The height of dominant tress, which ranged from 85 to 108 years of age, was 10.2m, and the largest tree 11.8m in height. Total basal area equaled 34.5m^2/ha. Leaf biomass was 12.4t/ha in summer or about 10t/ha in winter after leaffall. After a discussion on the average of 13.1±0.9t/ha of leaf biomass in winter, it was determined that the 10t/ha of winter leaf biomass was minimum in various Chamaecyparis obtusa forests with the close canopy. Annual leaffall rates for 4 years ranged from 1.65 to 2.72t/haã»y. Net production rate of aboveground parts was estimated 7.77t/haã»y, which accounted to about 50% of some plantations of the maximum growth
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æã¯ããçšåºŠã®çŽåŸãããã倪ãæã«æ®ã£ãŠããã1幎æã«çãåœå¹Žææ°ã¯å€ªãæã§å€ãã£ãããšãã, 倪ãæã§ã¯è³æºéãå€ãããšããããããããããéæ§åšå®ã¯æã®è³æºéãšã¯é¢ä¿ãªãççã, éæ§åšå®ã¯æã®è³æºéã«åœ±é¿ãããŠççããŠããããšãããã£ããThe relationships between the numbers of male flowers, female flowers and acorns produced on shoots and shoot diameter were studied in two 75-yr-old Quercus serrata trees. There was no relationship between the number of male flowers per current year shoot and the diameter of 1-yr-old shoots, while an increase was recognized in the number of female flowers per current shoot with increasing shoot diameter. The acorns survived on 1-yr-old shoots that exceeded a certain diameter. The number of current shoots on each 1-yr-old shoot increased with shoot diameter, suggesting an increase of resources in shoots with increasing size. Although no relationship between production of male flowers and shoot resources was found, there was a relationship between shoot resources and female flower-bearing and acorn development
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èŠã§ãããBasic studies on the germination and the mortality of HINOKI (Chamaecyparis obtusa ENDL.) seedlings were performed on the nursery of the Kyoto Prefectural University and the forest land of Yase, Sakyo-ku, Kyoto. The results obtained are as follows : 1. The seedling of HINOKI begins to germinate when the average temperature comes to about 15â (it is in the second and the third ten days of April in the forest land of Yase), and the greater part of germination comes to an end in July. 2. When the temperature and the soil moisture are sufficient for the germination, the relative lux about 30% is most suitable for it. It is restrained at 100% lux, and seems to be difficult under 5%. 3. The mortality of seedlings is highest from July to August, and the causes for the mortality are different according to the forest environment. In the place where A_0 layer is thin and A layer is shallow as the Yase experimental plot, the runing-off, burial and fall of seedlings caused by rain come to increase. In the forest land where A_0 layer is thick, it is assumed that insect and drought damage becomes more than that caused by rain. The frost damage for hibernal seedlings seems to be comparatively little. 4. Future study is necessary because the environment for the germination of the seeds of HINOKI differs from the environment of growth
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§)ã暹幹ã«äžããŠ, çŽ1çè²æéã®æé·ãžã®åœ±é¿ã調ã¹ããå®éšçµæãèŠçŽãããšã€ãã®ãšããã§ããã1)æ¯åã«ãã£ãŠæš¹é«æé·ã¯æžå°, çŽåŸæé·ã¯å¢å ã, ãããŠH/Dã¯æžå°ãããçæäžéšã®å¹¹æé¢ç©æé·ã¯, æ¯åã§äžæ¹ã»ã©èããä¿é²ãããããããæš¹å å
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šäœã§ãããããããã®åŸåã¯äžæ¹ã»ã©å€§ããã3)æ ¹éããã³æ ¹ã®å²åã¯æ¯åã«ãã£ãŠå¢å ããããšãã«æ¯ææ ¹ã§èããåŸåããã, ãããæ¯åæ¹åã«çºéããŠèæ¯åæ§ã倧ãããªã£ãã4)å
šæš¹äœ, å°äžéš, å¹¹æèã®åééã«å¯ŸããåŠçã®åœ±é¿ã¯ã°ãã°ãã§ãã£ãã, æ¯åã§ä¹Ÿç©çç£ãæžå°ããããšã¯ãªãã£ããå¹¹æèã®ãããå²åã¯æ¯åã«ãã£ãŠé¡èãªå€åããããããªããT/Rã¯ã€ã·ã£ãã·ã§åŠçå¹æããªã, ã€ããã³ããã®å®éšã§ã¯æ¯åèªç¶>åºå®ã§å10%å·®ã ã£ããThe effects of three mechanical stimulations : shaking, staying, and free-swaying (control), on the growth and development of young alder trees were studied. The period of the treatments was from 72 to 108 days. The summary of the results are as follows. 1) The shaking reduced height growth, enhanced diameter growth, and consequently decreased the ratio of height to diameter. Stem crosssectional area increment on clear bole was markedly increased by shaking, with the increase toward the stem base. The stayed trees showed a pronounced upward shift of increment, at the expense of downward stem parts. 2) Trees responed to unidirectional shaking by producing larger diameter increment along the shaking direction throughout their length, with increasing on the lower stem. 3) The effects of shaking affected growth by altering weight and percentage of roots, especially for larger roots more than 0.2cm in diameter. The root system was reflected by the development in direction to the stem shaking. 4) Although the evident tendency of the effects of the mechanical treatments on the dry weight of stem, branches, leaves, above-ground parts, and a whole tree has not become visible, the shaking did not reduced dry matter production. With the exception of root growth, the shaked and stayed trees did not alter the distribution of dry weight of each organ within the tree. The ratio of above-ground parts to root of a Alnus firma tree was not affected by shaking, but for A. hirsuta var. sibirica, the value resulted in decrease for shaken trees and in increase for stayed. 5) In the stayed treatment where A. hirsuta var. sibirica trees were prevented from swaying throughout their length, the stem bending was observed after the tree stakes were removed. Mean bulk density of stems spaned a range from 0.37g/(cm)^3 for shaking to 0.31g/(cm)^3 for staying
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ãœã€ã«ããã¡ãŒã¿ãçšããŠãããã®ããç©ã®åžæ°Žéã枬å®ããäžé£ã®å®éšã®çµæã次ã®ããã«ç·æ¬ãããããç©ã®åžæ°Žé床(ml/ããç©ã»æ¥, ãããã¯ml/g(ããç©ä¹Ÿé)ã»æ¥)ã®çµæå€åã®ãã¿ãŒã³ã¯, çžå¯Ÿçã«é«ãå€ã瀺ããå€åã®å€§ãã第äžæ®µé, ã€ãã§é£ç¶çãªäœäžã瀺ã第äºæ®µé, æåŸã«äœäžåŸåã®åæ¢ã«ãã暪ã°ã, ãããã¯äžæã®åŸåã瀺ã第äžæ®µéã®, 3ã€ã®æ®µéãåºå¥ããããšãã§ããããã®åžæ°Žé床ã®çµæå€åã¯, åå£éšåã®éæ°Žã®æµæ, ããã³çºæ ¹éã®ããããã®èŠå ã«, æ°è±¡æ¡ä»¶ã®åœ±é¿ãå ãã£ãŠããããããã®ãšã¿ããããåžæ°Žéãå€ããªãããšã¯çºæ ¹ã«ãšã£ãŠæãŸããæ¡ä»¶ãšãªãã®ã§, ãããã®ããæšãè¡ãªãã«ããã£ãŠã¯, åžæ°Žéãé«ããããã«æ°Žåç°å¢, ãšãã«åå£æ°Žåæ¡ä»¶ã«èæ
®ãã¯ãããªããã°ãªããªããWater absorption of Chamaecyparis obtusa cuttings was measured by using soil potometers for several years, and relation between water absorption and rooting of cuttings was investigated. Three typical stages for water absorption rate (ml/cuttingã»day, or ml/g d.w.ã»day) were observed. Namely, water absorption rate showed relatively high values in the early stage, then decreased continuously (second stage), and lastly remained on the same level or conversely increased gradually (third stage). It was considered that above-mentioned changes in water absorption rate arose from following three factors, those were resistance of cut base for that water passes, rooting results, and weather conditions. Active water absorption is one of the conditions necessary to obtain desirable rooting results. When cutting of Chamaecyparis oblusa is carried out, careful consideration for external moisture condition, especially soil water condition is needed