• 한국연초학회지
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• 제19권1호
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• pp.70-75
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• 1997

The expansive properties of leaf tobacco by nitrogen gas was investigated with cut tobacco AB3O-1, CD3L-1(NC82). Major factors for the best expansion of the tobacco by the gas were an impregnated pressure and expansion temperature. The expansion rate for AB3O-1 and CD3L-1 at 250℃, 750kg/cm2 was 96.6%, 99.4% respectively. The shred size and fineness index at 96.6% of expansion rate for AB3O-1 was almost the same as at 58.3% for CD3L-1. The time reaching at equilibrium moisture under of RH 57% was 36hr in non-treated leaf tobacco, but it was 20hr in expanded tobacco. We confirmed that total sugar contents of leaf tobacco by the expansion was decreased with 9.3∼10.9%. Total alkaloid was decreased with 17.5∼21.1% and ether extracts was declined with 4.9∼9.3%. These results suggest that the expansion method of leaf tobacco by nitrogen gas is a useful method without any serious environmental troubles. Key words : expansion, nitrogen gas, heat treatment, tobacco.

• The Korean Journal of Ecology
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• 제17권1호
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• pp.37-47
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• 1994

온대낙엽수립에서 목본식물의 개엽형태와 생육초기 생장과정을 분석하기 위하여 경기도 광주군 중부면 산성리 남한산성 구내의 자연림에서 1992.4.1~1992,5,31에 11종에 대하여 잎의 형태변화, 엽면적 및 잎의 건중량 변화를 조사하였다. 겨울누의 인편이 탈락한 후 잎의 전개형태는 크게 주맥과 측맥의 각도가 증가하는 형태, 2절이 펴지는 형태 및 주맥으로부터 말려 펴지는 형태와 3부류로 구분되었다. 잎의 전개시에 비하여 생장이 완료된 시기의 엽면적이 가장 크게 증가하는 종은 생강나무(4.2배)였고, 가장 적은 것은 개서나무(1.3배)였으며, 이것은 잎의 전개형태와 관게가 깊었다. 조사된 대부분의 수종에서4월 하순과 5월 중순에 엽면적상 생장은 완료되었지만 잎의 건중량은 조사기간 중 계속 증가하였다. 비엽면적의 최대치는 4월 중순과 5월 초순 사이에 나타나 엽면적 생장의 완료시보다 대략 10일 빨랐다. 그리고, 5월 하순에 비엽면적의 값은 관목은 200cm2/g이상이었고 교목은 200cm2/g이하이었다.

• 한국환경과학회지
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• 제22권10호
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• pp.1345-1351
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• 2013

Leaf characteristics of two representative deciduous-tree species in Korean peninsula were compared to assess directional ridge effect on leaf traits of both species. Leaf mass per unit area (LMA) of Rhododendron schilippenbachii in south-facing ridge slope was significantly higher than that in north-facing ridge slope, while Quercus mongolica did not change LMA. Leaf mass of Q. mongolica was increased depending on leaf size irrespective of slope. However, leaf mass of R. schilippenbachii changed differently in responding to expansion of leaf area between both slopes resulting from retardation of leaf expansion in south-facing slope. R. schilippenbachii showed higher leaf nitrogen concentration per unit area (LNCA) in south-facing slope than that in north-facing slope, while Q. mongolica indicated no difference in LNCA between southand north-facing slopes. However, both species revealed no significant difference in leaf nitrogen concentration per unit mass (LNCM) between south- and north-facing slopes. LNCA of Q. mongolica was about two times higher than that of R. schilippenbachii. These results indicate that there is a difference in leaf characteristics including leaf thickness and nitrogen allocation between Q. mongolica and R. schilippenbachii, suggesting the difference of plasticity.

• Journal of Plant Biotechnology
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• 제5권3호
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• pp.137-142
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• 2003

The morphology of the leaves and the flowers of angiosperms exhibit remarkable diversity. One of the factors showing the greatest variability of leaf organs is the leaf index, namely, the ratio of leaf length to leaf width. In some cases, different varieties of a single species or closely related species can be distinguished by differences in leaf index. To some extent, the leaf index reflects the morphological adaptation of leaves to a particular environment. In addition, the growth of leaf organs is dependent on the extent of the expansion of leaf cells and on cell proliferation in the cellular level. The rates of the division and enlargement of leaf cells at each stage contribute to the final shape of the leaf, and play important roles throughout leaf development. Thus, the control of leaf shape is related to the control of the shape of cells and the size of cells within the leaf. The shape of flower also reflects the shape of leaf, since floral organs are thought to be a derivative of leaf organs. No good tools have been available for studies of the mechanisms that underlie such biodiversity. However, we have recently obtained some information about molecular mechanisms of leaf morphogenesis as a result of studies of leaves of the model plant, Arabidopsis thaliana. For example, the ANGUSTIFOLIA (AN) gene, a homolog of animal CtBP genes, controls leaf width. AN appears to regulate the polar elongation of leaf cells via control of the arrangement of cortical microtubules. By contrast, the ROTUNDIFOLIA3 (ROT3) gene controls leaf length via the biosynthesis of steroid(s). We provide here an overview of the biodiversity exhibited by the leaf index of angiosperms. Taken together, we can discuss on the possibility of the control of the shapes and size of plant organs by transgenic approaches with the results from basic researches. For example, transgenic plants that overexpressed a wildtype ROT3 gene had longer leaves than parent plants, without any changes in leaf width. Thus, The genes for leaf growth and development, such as ROT3 gene, should be useful tools for the biodesign of plant organs.

• 한국식물생명공학회:학술대회논문집
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• 한국식물생명공학회 2003년도 식물바이오벤처 페스티발
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• pp.49-55
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• 2003

The morphology of the leaves and the flowers of angiosperms exhibit remarkable diversity. One of the factors showing the greatest variability of leaf organs is the leaf index, namely, the ratio of leaf length to leaf width. In some cases, different varieties of a single species or closely related species can be distinguished by differences in leaf index. To some extent, the leaf index reflects the morphological adaptation of leaves to a particular environment. In addition, the growth of leaf organs is dependent on the extent of the expansion of leaf cells and on cell proliferation in the cellular level. The rates of the division and enlargement of leaf cells at each stage contribute to the final shape of the leaf, and play important roles throughout leaf development. Thus, the control of leaf shape is related to the control of the shape of cells and the size of cells within the leaf. The shape of flower also reflects the shape of leaf, since floral organs are thought to be a derivative of leaf organs. No good tools have been available for studies of the mechanisms that underlie such biodiversity. However, we have recently obtained some information about molecular mechanisms of leaf morphogenesis as a result of studies of leaves of the model plant, Arabidopsis thaliana. For example, the ANGUSTIFOLIA (AN) gene, a homolog of animal CtBP genes, controls leaf width. AN appears to regulate the polar elongation of leaf cells via control of the arrangement of cortical microtubules. By contrast, the ROTUNDIFOLIA3 (ROT3) gene controls leaf length via the biosynthesis of steroid(s). We provide here an overview of the biodiversity exhibited by the leaf index of angiosperms. Taken together, we can discuss on the possibility of the control of the shapes and size of plant organs by transgenic approaches with the results from basic researches. For example, transgenic plants that overexpressed a wild-type ROT3 gene had longer leaves than parent plants, without any changes in leaf width. Thus, The genes for leaf growth and development, such as ROT3 gene, should be useful tools for the biodesign of plant organs.

• 한국연초학회지
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• 제21권2호
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• pp.144-151
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• 1999

This study was carried out to compare the change physico-chemical properties in the 10 grades of Burley leaf tobacco expanded by $CO_2$. The filling capacity of AB3T was increased from 5.44cc/g to 9.52cc/g with the expansion rate 75.0% and that of CD3W was increased from 5.57cc/g to 10.16cc/g with the expansion rate 82.4%. But the rate of cut tobacco longer than 3.36 mm decreased from 77.2% to 49.9% and from 67.3% to 41.2% in grade B1T and C1W, respectively. The contents of nicotine and total volatile base in the of expanded cut tobacco decreased 11.9% and 10.4% respectively. The contents of onganic acids, except oxalic and palmitic acid, essential oil, amino acids, nicotine, tar and ammonia contents in the cigarette smoke decreased by expansion procecs. These results suggest that expanded tobacco was very useful to make less irritative cigarettes.

• Journal of Plant Biotechnology
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• 제38권4호
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• pp.285-292
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• 2011

식물 잎의 발달과정에서 heteroblasty는 외부 환경에 대한 식물의 형태적 적응 방법을 매우 잘 반영하며 이에 따른 변화는 기관의 최종 형태와 크기에 영향을 미친다. Heteroblasty를 나타내는 인자 중에서 leaf index는 단엽식물의 잎의 최종 모양과 크기를 나타내는 대표적인 인자이다. Leaf index는 결국 잎몸에서의 세포 증식과 세포 신장의 두 요인에 의해 결정된다. 비록 세포의 증식과 신장을 조절하는 유전자와 조절 기작들이 연구되고 있으나 큰 청사진을 제시하기에는 아직 미흡하다. 본 연구에서는 발달과정 중 잎의 leaf index 조절에 관여하는 유전자를 밝히고 그 조절 기작을 알아내기 위하여 애기장대 돌연변이체를 이용한 분자유전학적, 생리학적인 실험을 수행하였다. 잎과 잎 세포가 커지는 돌연변이체인 macrophylla (mac)를 선발하여 잎의 확장과정과 leaf index의 이상으로 인해 잎 기관의 모양뿐 만 아니라 heteroblasty에 변화가 발생했다는 사실을 밝혀냈다. 또한 이 돌연변이체는 기존에 알려진 ROTUNDIFOLIA3 (ROT3) 유전자의 점 돌연변이에 의해 일어났다고 판명되었고 mac/rot3-5로 명명되었다. 브라시노스테로이드 처리로 인해 ROT3 유전자의 발현이 음성 되먹임 저해를 받는 것으로 보아 ROT3 유전자가 브라시노스테로이드 생합성에 관여함을 제시하였다. 또한 암상태에서 ROT3 유전자의 발현이 증가하며, mac/rot3-5 돌연변이체가 야생형보다 암반응이 약하게 나타났다. 이러한 분석 결과를 토대로 본 논문은 ROT3 유전자가 잎의 확장과정에서 잎의 leaf index 조절과 고유한 heteroblasty의 정립에 중요한 역할을 수행하며, 브라시노스테로이드 호르몬의 조절을 통하여 음지회피성과 같은 환경조절반응을 수행하고 있다는 새로운 사실을 제시하였다.

• 식물분류학회지
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• 제37권4호
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• pp.351-361
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• 2007

In angiosperms, leaves typically develop as three-dimensional structure with dorsoventral, longitudinal, and lateral axes. We have shown that the control of two axes of leaves, longitudinal and lateral axis, can be genetically separable, and four classes of genes are responsible for the polar cell expansion and polar cell proliferation in Arabidopsis. In monocots, unifacial leaf, in which leaf surface consists only of abaxial identity, has been evolved in a number of divergent species. The unifacial leaves provide very unique opportunities for the developmental studies of the leaf axes formation in monocots, because their leaf polarities are highly disorganized. In addition, the mechanism of the parallel evolution of such drastic changes in leaf polarities is of interest from an evolutionary viewpoint. In this article, we describe our recent approaches to reveal the mechanism of unifacial leaf development and evolution, including recent advances in the leaf polarity specification in angiosperms.

• KSII Transactions on Internet and Information Systems (TIIS)
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• 제8권3호
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• pp.873-889
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• 2014

IP address lookup is very crucial in performance of routers. Several works have been done on prefix caching to enhance the performance of IP address lookup. Since a prefix represents a range of IP addresses, a prefix cache shows better performance than an IP address cache. However, not every prefix is cacheable in itself. In a prefix cache it causes false hit to cache a non-leaf prefix because there is possibly the longer matching prefix in the routing table. Prefix expansion techniques such as complete prefix tree expansion (CPTE) make it possible to cache the non-leaf prefixes as the expanded forms, but it is hard to manage the expanded prefixes. The expanded prefixes sometimes incur a great deal of update overhead in a routing table. We propose a bitmap-based prefix cache (BMCache) to provide low update overhead as well as low cache miss ratio. The proposed scheme does not have any expanded prefixes in the routing table, but it can expand a non-leaf prefix using a bitmap on caching time. The trace-driven simulation shows that BMCache has very low miss ratio in spite of its low update overhead compared to other schemes.

• 식물분류학회지
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• 제49권1호
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• pp.1-7
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• 2019

Early leaves within the Viola albida complex were investigated by scanning electron microscopy in order to determine the morphological segments during morphogenesis. The early leaf development of V. albida var. albida could be morphologically divided into the eight stages in the following order: I, the initiation of shoot germination; II, the conical growth directionally of the leaf; III, the adaxial and abaxial formation of the leaf; IV, the initiation of the stipule; V, the formation of a transitional zone between the leaf blade and petiole; VI, the expansion of the upper part of the leaf blade; VII, the formation of almost all parts of the early leaf; VIII, the early simple leaf. Viola albida var. takahashii differs from V. albida var. albida by additional stages, i.e., V-1, the initiation of the first lateral lobe at the both lateral parts of the leaf after the stage V and an early lobed leaf. Viola albida var. chaerophylloides is also distinguished from two taxa by two developmental features, V-2, the initiation of a second lateral lobe below of the first lateral lobe, and an early palmately compound leaf. These findings suggest that the Viola albida complex would be in the process of peramorphosis, showing developmental changes in a chain of events, leading to a different leaf shape. These data would also be useful for isolating genes that give rise to different leaf morphogenesis outcomes among the taxa in the Viola albida complex.