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21.
Michael Nee 《Brittonia》1994,46(4):265-269
Talauma boliviana is described as new and illustrated. This species, first collected in 1989, is the only Magnoliaceae known from Bolivia. It seems to be most closely related toT. sambuensis of northwestern Colombia and eastern Panama.  相似文献   
22.
One new bourbonane-type (1) and one new cadinane-type (2) sesquiterpenoids, along with one known aromodendrane-type (3) and five known megastigmane-type (48) compounds, were isolated from the leaves and twigs of Manglietia aromatica, a Chinese endangered plant that has not been previously phytochemically investigated. The structures and absolute configurations of the new isolates, (1R,4S,5S,6S,7S,10S)-4-hydroxy-bourbon-8-one (1) and (1R,6S,7S)-1-hydroxy- cadin-4,9-dien-8-one (2), were established by means of spectroscopic methods and a combination of experimental and calculated electronic circular dichroism (ECD). Among the isolates, compound 2 was found to show a moderate inhibitory effect against the human protein tyrosine phosphatase 1 B (PTP1B) enzyme, a target for the treatment of type-II diabetes and obesity, with an IC50 value of 83.5 μM.  相似文献   
23.
根据对广东木莲Manglientia kwangtungensis(Merr.)Dandy和毛桃木莲M.moto Dandy大量标本的研究,将毛桃木莲处理为广东木莲的一个异名。  相似文献   
24.
Spiral thickenings in the inner walls of vessels were studied in 10 genera 69 species of Magnoliaceae in China under scanning electron microscopic observation. Spiral thickenings were found in some species. The majority of these species showed complete thickenings of the inner wall, however, in some of which the spiral thickenings were less obvious at both ends. In others, these spiral thickenings existed only in the middle portion, uniformly or irregularly distributed.  相似文献   
25.
A new system of classification of Magnoliaceae proposed. This paper deals mainly with taxonomy and phytogeography of the family Magnoliaceae on the basis of external morphology, wood anatomy and palynology. Different authors have had different ideas about the delimitation of genera of this family, their controversy being carried on through more than one hundred years (Table I). Since I have been engaged in the work of the Flora Reipublicae Popularis Sinicae, I have accumulated a considerable amount of information and material and have investigated the living plants at their natural localities, which enable me to find out the evolutionary tendencies and primitive morphological characters of various genera of the family. According to the evolutionary tendencies of the characters and the geographical distribution of this family I propose a new system by dividing it into two subfamilies, Magnolioideae and Liriodendroideae Law (1979), two tribes, Magnolieae and Michelieae Law, four subtribes, Manglietiinae Law, Magnoliinae, Elmerrilliinae Law and Micheliinae, and fifteen genera (Fig. 1 ), a system which is different from those by J. D. Dandy (1964-1974) and the other authors. The recent distribution and possible survival centre of Magnoliaceae. The members of Magnoliaceae are distributed chiefly in temperate and tropical zones of the Northern Hemisphere, ——Southeast Asia and southeast North America, but a few genera and species also occur in the Malay Archipelago and Brazil of the Southern Hemisphere. Forty species of 4 genera occur in America, among which one genus (Dugendiodendron) is endemic to the continent, while about 200 species of 14 genera occur in Southeast Asia, of which 12 genera are endemic. In China there are about 110 species of 11 genera which mostly occur in Guangxi, Guangdong and Yunnan; 58 species and more than 9 genera occur in the mountainous districts of Yunnan. Moreover, one genus (Manglietiastrum Law, 1979) and 19 species are endemic to this region. The family in discussion is much limited to or interruptedly distributed in the mountainous regions of Guangxi, Guangdong and Yunnan. The regions are found to have a great abundance of species, and the members of the relatively primitive taxa are also much more there than in the other regions of the world. The major genera, Manglietia, Magnolia and Michelia, possess 160 out of a total of 240 species in the whole family. Talauma has 40 species, while the other eleven genera each contain only 2 to 7 species, even with one monotypic genus. These three major genera are sufficient for indicating the evolutionary tendency and geographical distribution of Magnoliaceae. It is worthwhile discussing their morphological characters and distributional patterns as follows: The members of Manglietia are all evergreen trees, with flowers terminal, anthers dehiscing introrsely, filaments very short and flat, ovules 4 or more per carpel. This is considered as the most primitive genus in subtribe Manglietiinae. Eighteen out of a total of 35 species of the genus are distributed in the western, southwest to southeast Yunnan. Very primitive species, such as Manglietia hookeri, M. insignis and M. megaphylla, M. grandis, also occur in this region. They are distributed from Yunnan eastwards to Zhejiang and Fujian through central China, south China, with only one species (Manglietia microtricha) of the genus westwards to Xizang. There are several species distributing southwards from northeast India to the Malay Archipelago (Fig. 7). The members of Magnolia are evergreen and deciduous trees or shrubs, with flowers terminal, anthers dehiscing introrsely or laterally, ovules 2 per carpel, stipule adnate to the petiole. The genus Magnolia is the most primitive in the subtribe Magnoliinae and is the largest genus of the family Magnoliaceae. Its deciduous species are distributed from Yunnan north-eastwards to Korea and Japan (Kurile N. 46’) through Central China, North China and westwards to Burma, the eastern Himalayas and northeast India. The evergreen species are distributed from northeast Yunnan (China) to the Malay Archipelago. In China there are 23 species, of which 15 seem to be very primitive, e.g. Magnolia henryi, M. delavayi, M. officinalis and M. rostrata, which occur in Guangxi, Guangdong and Yunnan. The members of Michelia are evergreen trees or shrubs, with flowers axillary, anthers dehiscing laterally or sublaterally, gynoecium stipitate, carpels numerous or few. Michelia is considered to be the most primitive in the subtribe Micheliinae, and is to the second largest genus of the family. About 23 out of a total of 50 species of this genus are very primitive, e.g. Michelia sphaerantha, M. lacei, M. champaca, and M. flavidiflora, which occur in Guangdong, Guangxi and Yunnan (the distributional center of the family under discussion) and extend eastwards to Taiwan of China, southern Japan through central China, southwards to the Malay Archipelago through Indo-China. westwards to Xizang of China, and south-westwards to India and Sri Lanka (Fig. 7). The members of Magnoliaceae are concentrated in Guangxi, Guangdong and Yunnan and radiate from there. The farther away from the centre, the less members we are able to find, but the more advanced they are in morphology. In this old geographical centre there are more primitive species, more endemics and more monotypic genera. Thus it is reasonable to assume that the region of Guangxi, Guangdong and Yunnan, China, is not only the centre of recent distribution, but also the chief survival centreof Magnoliaceae in the world.  相似文献   
26.
综述了中国木兰科10属的次生木质部解剖学特征,包括导管分子,纤维管胞和木射线。同时,进一步讨论了其系统演化。这10属分为两亚科,即:木兰亚科(Magnoliodeae),包括木兰族(Magnolieae)和含笑族(Michelieae Law),木兰族有木莲属(Maglietia Bl.)、华盖木属(Manglietiastrum Law)、木兰属(Magnolia L.)、拟单性木兰属(Parakmeria Hu et Cheng)、单性木兰属[Kmeria(Pierre) Dandy]、长蕊木兰属(Alcimandra Dandy)共六属;含笑族有含笑属(Michelia L.)、合果木属(Paramichelia Hu)、观光木属(Tsoongiodendron Chun)共三属。鹅掌楸亚科[Liriodendroideae(Bark) Law],仅鹅掌楸属(Liriodendron L.)一属。大量的木材解剖学研究表明,木兰科的原始性很明显,但也有一些进化特征。可以通过属间的差别来分析本科的系统演化。木兰科的系统演化可简单总结为:木兰亚科[木兰族(木莲属,华盖木属,拟单性木兰属,单性木兰属→木兰属,长蕊木兰属)→含笑族]→鹅掌楸亚科。  相似文献   
27.
The leaf structure and morphology, the structure and location of oil cells in leaves of 82 species and 1 subspecies in 10 genera of the Magnoliaceae were comparatively studied using tissue clearing, paraffin sectioning and thin sectioning. In leaves of Liriodendroideae, some of abaxial epidermal cells are papillose and the vascular tissue of the main vein appeared to be separated. However, papillose cells were not found and there were uniseriate, multicellular or unicellular hairs distributed on the epiderm, and the vascular tissue of the main vein appeared to be continuous in leaves of the Magnolioideae. Furthermore, in the Magnolioideae, the structure of leaves of Manglietia were different from that of Magnolia. These results support the separation of Magnolioideae and Liriodendroideae, and suggest that Manglietia and Magnolia be independent genera, which is consistent with Law’ s taxonomic scheme. Oil cells are one of marked features of the leaf anatomy of the Magnoliaceae, and they are mainly distributed in the palisade tissue in leaves of 47 species and in the spongy tissue in leaves of 5 species, and dispersed in the whole mesophyll in leaves of 31 species. The size and location of oil cells in leaves, combined with the thickness of leaves, the number of layers of the palisade tissue, the ratio of palisade tissue to spongy tissue in thickness, the hypo-derm, and the type of hairs may be used as the characteristics of genera and even species.  相似文献   
28.
焕镛木属——中国木兰科一新属   总被引:14,自引:0,他引:14  
刘玉壶 《植物研究》1997,17(4):353-356
焕镛木属(Woonyoungia Law)曾分布于广西西北部罗城县,现星散分布于广西北部环江县,贵州省东部荔坡县、云南西南部马关县、是珍稀濒危树种。焕镛木属的花单性异株,与木兰科其他各属均不同;雄花的花被片形态相似而雌花的花被片则明显异形,这也是与木兰科其他各属均不同。此外,焕镛木属的雄蕊两药室稍分开,内侧向开裂,药隔伸出成舌状尖;雌蕊6-9,心皮全部合生,仅露出柱关面;成熟心皮革质,沿背缝开裂,形成近球形的聚合果。与它近缘的单性木兰属(Kmeria Dandy)则雄蕊两药室紧贴,内向开裂,顶端钝,药隔不伸出;成熟心皮木质、沿腹缝全裂及顶端开裂,最后裂成两果瓣、形成各成熟心皮散开的聚合果等不同。依上述不相同特征,故成立焕镛木属属新属。  相似文献   
29.
Three new phenylethanoid glycosides, 2-(3-hydroxy-4-methoxyphenyl)ethyl 1-O-β-d-allopyranoside (hodgsonialloside A, 1), 2-(3-hydroxy-4-methoxyphenyl)ethyl 1-O-β-d-glucopyranosyl-(1  4)-β-d-allopyranoside (hodgsonialloside B, 2) and 2-(3-methoxy-4-hydroxyphenyl)ethyl 1-O-β-d-allopyranoside (hodgsonialloside C, 3) were isolated from the leaves of Magnolia hodgsonii in addition to six known compounds, tyrosol 4-O-β-d-xylopyranosyl-(1  6)-β-d-glucopyranoside (4), kaempferol 3-O-neohesperidoside (5), kaempferol 3-O-rutinoside (6), kaempferol 3-O-α-l-rhamnopyranosyl-(1  2)-[α-l-rhamnopyranosyl-(1  6)]-β-d-glucopyranoside (7), (+)-syringaresinol O-β-d-glucopyranoside (8), and oblongionoside C (9). The structure elucidation of these compounds was based on analyses of physical and spectroscopic data including 1D and 2D NMR experiments.  相似文献   
30.
Three undescribed flavonol triglycosides, rhamnetin-3-O-α-L-rhamnopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→6)]-β-d-glucopyranoside (champaluangoside A), rhamnetin-3-O-α-l-rhamnopyranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→6)]-β-d-galactopyranoside (champaluangoside B) and rhamnocitrin-3-O-α-l-rhamnopyranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→6)]-β-d-glucopyranoside (champaluangoside C), were isolated from Magnolia utilis in addition to eleven known compounds; quercetrin-3-O-α-l-rhamnopyranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→6)]-β-d-glucopyranoside, oxytroflavoside G, magnoloside A, magnoloside M, magnoloside D, manglieside A, manglieside B, 1,2-di-O-β-d-glucopyranosyl-4-allylbebzene, syringrin, benzyl β-d-allopyranoside and (+)-syringaresinol-O-β-d-glucopyranoside. The structure elucidation of these compounds was based on analyses of physical and spectroscopic data.  相似文献   
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