• 식물분류학회지
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• 제42권4호
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• pp.267-274
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• 2012

흰대극과 섬흰대극의 형태적, 유전적 분화를 알아보기 위해 두 종의 14개 자연 집단으로부터 12개의 형태형질과 11개의 동위효소 유전좌위를 조사하였다. 흰대극복합체의 유전적 다양성 측정치(A=1.63, P=44.83, $H_e$=0.198)는 기존의 동북아산 암대극과 두메대극의 보고와 유사하며, 한국산 붉은대극과 대극보다는 약간 낮은 수치를 보여주고 있다. 비록 대부분 두 종사이의 형태형질의 측정범위가 중복되나 흰대극과 섬흰대극은 형태형질의 조합에 의해 구별되며, 이를 기초로 한 전형질도는 한국에 두 종이 분포함을 지지해주고 있다. 하지만 동위효소 자료를 이용한 분석에서는 두 종이 구별되지 않았으며, 이와 같은 두 자료의 불일치는 두 종이 최근에 분화 하였거나 종간 형질이입에 의한 교잡에 의해 이와 같은 결과가 나온 것으로 추측된다.

• 한국환경복원기술학회지
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• 제16권3호
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• pp.83-95
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• 2013

To understand natural regeneration and stand development after fire in mixed broadleaved-coniferous forests of Sikhote-Alin Mountains, ten sample plots of $50m{\times}50m$ size were established in 1975 and 1983 at the stands burned by wildfires in 1973 and 1982, respectively. And, the number of naturally regenerated seedlings were monitored in two $50m{\times}4m$ subplots in each plot. The most fire-sensitive conifer species is Abies nephrolepis, while Betula costata is the most fire-sensitive broadleaved tree species. The most fire-resistant species were Q. mongolica, T. taquetii and A. mono. The results of 20 and 30 years after the fire showed that pioneer tree species, e.g. Populus, Salix, and Betula, were regenerated immediately at the early stage of stand development and grew where there is a mono canopy layer with high density. On the other hand, the densities of successors, e.g. Pinus koraiensis, Picea jezoensis, Abies nephrolepis, Acer mono and Tilia taquetii, which were present in the study plots before the fire, increased gradually. Naturally regenerated tree species after forest fire by the growth rate were divided into three groups according to their annual height growth. The seral tree species (Betula costata, Betula platyphylla, Padus maackii, Populus tremula and Sarix caprea) belong to the first group and have the highest growth rate (from 40 to 96 cm per year). The late successional broad-leaved trees (Tilia taquetii, Acer mono and Quercus mongolica) belong to the second group and have intermediate annual height growth (from 3.7 to 13.5 cm per year). The late successional coniferous species (Picea jezoensis, Pinus koraiensis and Abies nephrolepis) form the third group and have the least annual height growth (from 1.4 to 3.5 cm per year).

• The Korean Journal of Physiology
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• 제9권1호
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• pp.13-22
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• 1975

From the study of movements of $Ca^{++}$ in frog cardiac muscle, Niedergerke (1963) postulated that $Ca^{++}$ necessary for the cardiac contraction is stored in a specific pool. Langer et al (1967) and DeCaro (1967) also found a close relationship between the change of $Ca^{++}$ flux kinetics and the change of contractile force. According to the studies of several investigators, Ca II (Bailey and Dressel 1968) or phase I and II (Langer 1965, Langer et al 1967, 1971) in the $Ca^{++}$ washout curve was associated with cardiac contractility. This investigation was aimed to elucidate the anatomical region of the contractile active $Ca^{++}$ pool. At the same time, it was assumed in this study that $Ca^{++}$ in the sarcoplasmic reticulumn represents one of the major intracellular $Ca^{++}$ pool and cardiac contractility was also dependent on the intracellular $Ca^{++}$ concentration. Consequently, this experiment was performed at different temperatures to activate to activate inhibit the deactivating process of activated $Ca^{++}$ in the intracellular space to see if changes in the contractility decay curve existed at different temperatures. The isolated hearts of rabbits and turtles (Amyda maackii) were attached to the perfusion apparatus according to the method employed by Bailey and Dressel (1968). The isolated hearts were initally perfused with a full Ringer solution containing 2 mg/ml of inulin for 1 hr, and then $Ca^{++}$ and inulin-free Ringer solution was perfused while the isometric tension was recorded and a serial sample of perfusion fluid dripping from the cardiac apex was collected for 10 sec throughout experimental period. The above procedure was performed at $23^{\circ}C$, $30^{\circ}C$ and $38^{\circ}C$ on the rabbit heart and $10{\sim}13^{\circ}C$, $10^{\circ}C$, $25^{\circ}C$, $30^{\circ}C$ and $35^{\circ}C$ on the turtle heart. After determination of $Ca^{++}$ and inulin concentration of the samples, the $Ca^{++}$, inulin washout curve and the contractile tensin decay curve were analysed according to the method of Riggs (1963). The results were summarized as follows; 1. In the rabbit heart, there are 2 inulin compartments, 3 $Ca^{++}$ compartments and sing1e exponential decay of contractile tension. In the turtle heart, there are $1{\sim}2$ inulin compartments, $1{\sim}2$ $Ca^{++}$ compartments and $1{\sim}2$ phases of contractile tension decay. The fact that the inulin space was divided into 3 compartments in the washout curve in these hearts indicates the presence of heterogeneity in cardiac perfusion, i.e., overfused and underperfused area. 2. Ca I a9d Ca II in these hearts were found to have $Ca^{++}$ in the ECF compartments because their half times in the washout curves were far smaller than those of the inulin washout curves in the rabbit heart and similar to those of the inulin washout curves in the turtle heart. Ca III in the rabbit heart may have originated from the intracellular $Ca^{++}$ store. But no Ca III in the turtle heart was found. This may be due to the fact that the iutracellular $Ca^{++}$ pool in the turtle heart was too small to detect using this experimental procedure since sarcoplasmic reticulumn in the turtle heart is poorly developed. 3. In the rabbit heart, there were no chages in the half time of Ca I, Ca II, inulin I and inulin II at different temperatures, but the half time of Ca III was significantly prolonged at lower temperatures, and the half time of the contractile tension decay tended to be prolonged at lower temperatures but this was not significant. In the turtle heart, there were no changes in the half time of Ca I, Ca II, inulin 1, inulin II and phase I of the contractile tension decay at different temperatures, but the half time of phase II of the contractile tension decay was significantly prolonged at lower temperatures. This finding indicates that intracellu!ar $Ca^{++}$ in these hearts was also responsible particulary for maintaining the cardiac contractility at the lower temperatures. 4. The half times of contractile tension decay were shorter than those of Ca II in the $Ca^{++}$ washout curves in both animal hearts. According to the above results it was shown that $Ca^{++}$ in ECF is primarily and $Ca^{++}$ in the intracellular space is partially associated with the cardic contractility.