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    15 September 1985, Volume 5 Issue 3
    NEW TAXA OF BERBERIS LINN.FROM YUNNAN Bao Shih-ying
    Bao Shi-ying
    1985, 5(3):  1-35. 
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    A REVISION OF THE GENUS CHIRITA(GESNERIACEAE)IN CHINA(Ⅱ)
    Wang Wen-tsai
    1985, 5(3):  37-86. 
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    1. In the present paper 77 species of the genus Chirita are recognized from China. While accepting the classification con-structed by Wood (1974) and his sectional alignment for the time being, I attempt to give a putative interpretation to the affinities between the three large groups of this genus. The first, Sect. Gibbosaccus, retaining more primitive characters, may be regarded as the primitive one and the second, Sect.Chirita, distinguished from Sect. Gibbosaccus principally by its synsepalous calyx and larger stigma, is more advanced. On the other hand, the third group, Sect. Microchirita, being mono-carpic and having epiphyllous inflorescences and anthers cohe-rent at apex by a small appendage, is somewhat remote phy-logenetically from the other two and may represent an ano-ther evolutionary line. In addition, the important morpholo-ical characters are discussed and the infra-sectional subdivi-sion of Sect. Gibbosaccus and Sect. Chirita is made. A conspec-tus of the classification for the 77 Chinese species is given as follows.Sect. 1. Gibbosaccus. Herbs perennial, seldom annual, acaules-cent, seldom caulescent. Cyme not epiphyllous. Sepals free, seldom connate. Anthers fused face to face, exappendicula-te. Stigma small.Subsect. 1. Sinenses. Herbs perennial, acaulescent. Leaves more or less pubescent, ovate, elliptic or oblong, seldom linear.Ser. 1. Swinglianae. Corolla tube infundibuliform-tubular or campanulate. Filaments irregular. Stigma undivi-ded. (sp. 1-10).Ser. 2. Medicae. Corolla tube infundibuliform-tubular. Fi-laments regular. Stigma 2-lobed. (sp. 11-13).Ser. 3. Fimbrisepalae. Corolla large or moderate in size, with tke tube infundibuliform-tubular. Filaments irre-gular. Stigma 2-lobed. (sp. 14-48).Ser.4. Sinenses. Allied to the preceding series, differing in the bilocular ovary with the lower chamber reduced and sterile. (sp. 49).Ser. 5. Pinnatifidae Allied to the preceding series, differing in the pinnately lobed leaves. (sp. 50).Ser. 6. Pinnatae. Allied to Ser. Sinenses and Ser. Pinnati-fidae, differing in the pinnate leaves. (sp. 51).Ser. 7. Shennungjiaenses. Small herbs. Leaves small. Corol-la moderate in size or small, with the tube tubular or cylindric. Filaments often regular. Stigma 2-lobed or 2-fid, seldom undivided. (sp. 52-56).Ser. 8. Hedyotideac. Leaves narrow-oblong. Sepals conna-te. Corolla small. Filaments subregular. Stigma 2-10-bed. (sp. 57).Subsect. 2. Spinulosae. Herbs perennial, offen acaulescen with ligneous robust rhizomes. Leaves glabrous, linear, remotely spinulose-denticulate at margin. Corolla small. Stigma 2-lobed. (sp. 58-59).Subsect. 3. Cicatricosae. Herbs perennial or annual, caules-cent. Leaves opposite or alternate, ovate or elliptic, pubescent. (sp. 60-62).Sect. 2. Chirita. Allied to the preceding section, differing in the connate sepals and larger stigma.Subsect. 1. Briggsioides. Herbs perennial, acaulescent. Flo-wers arranged in pedunculate cyme. Stigma 2-lobed or 2-fid. (sp. 63-67).Subsect. 2. Urticifoliae. Herbs perennial, seldom annual, caulescent. Leaves opposite, seldom alternate. Flowers arranged in pedunculate cyme. Stigma 2-lobed or 2-fid, seldom undivided.Ser. 1. Urticifoliae. Bracts free. Filaments not tumid. (sp. 68-74).Ser. 2. Infundibuliformes. Bracts connate into a wide-infun-dibuliform involucre Filaments tumid at the middle part. (sp. 75).Subsect. 3. Fasciculiflorae Herbs perennial, caulescent. Lea-ves 3-4 pairs conferted at the stem apex. Flowers axillary. Stigma undivided. (sp. 76).Sect. 3. Microchirita. Herbs mostly annual, caulescent. Cyme epiphyl1ous. Anthers coherent by a small appendage at the apex. Stigma small, 2-fid (sp. 77). 2. The genus Chirita, containing about 120 species, occur in the warm parts of southeastern Asia. Wood (1974) designated southern China and Vietnam, eastern Himalayas to western China, and Thailand and Vietnam as the centres of distribu-tion of Sect. Gibbosaccus, Sect. Chirita and Sect. Microchiritarespectively.
    MATERIALS OF DAPHNE LINN.FROM CHINA
    Chang Che-yung
    1985, 5(3):  87-108. 
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    A STUDY ON THE TWO TYPES OF FLOWERS IN SCHNABELIA OLIGOPHYLLA HANDEL-MAZZETTI
    Su Song-wang
    1985, 5(3):  109-120. 
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    C. Chein (1964) discovered for the first time the two types of flowers, chasmogamous and cleistogamous in genus Schnabelia. Based on the materials available, he then pointed out that the problem whether the two types of flowers of the genus Schnabelia existed on the same individual plants or on the different individuals still remained unclear, and that they seemed to be on the different plants. The present research in to S. oligophylla Hand.Mazz.collected from Qimen of Anhui Province make it distinct that the two types of flowers undoubtedly exist on the same plant.So far as the time of their appearance is concerned, the chas-mogamous flowers precede the cleistogamous ones. As for their positions, they situated themelves separately on their own cy-mes, and come out of the leaf axils above the near base, at the same time the cleistogamous ones do out the lowest base of the chasmogamous flower's peduncle after these flowers wi-thering. The occurrence of the cleistogamous flowers probably has something to do with the inf1uence of the environmen-tal factors. Having transplanted some S. oligophylla from the growing area to Hefei, the author observed after potting it, that the flowers which came out in the year were chasmogamous, while the flowers that appeared early next year were chas-mogamous, and then came out the cleistogamous ones. As for manner of fertilization, a cleistogamous flower is ob-viously that of self-fertilization. The chasmogamous flowers, rich in colour, is suited to entomophilous pollination, but the surface of their anthers is covered with sparse arachnoid hairs. At the time when the alabustrum is just about flower, the top parts of the filaments incurved and the anthers con-tact with one another laterally to form a ring, through which the style just pierces when it extends. Nevertheless, the arachnoid hairs on the surface of the anthers adhere to the branchlets of the style. After flowering, the stamens and the style begin to stretch straight. From this phenomenon may be seen that the chasmogamous flowers probably have the self-fertilization capability, which, when the cross-pol-lination fails ensures the work of self-fertilization. It should be particularly pointed out that having studied the two types of flowers of the genus Schnabelia, the present writer discovered that the two types of flowers of Caryopteris nepetaefolia and Scutillaria indica have quite the same structure as those of the genus Schnabelia too. In the species with the two types of flowers, the manners of fertilization of flowers are altogether differently. Generaly the conspicusous flowers (chasmogamous) are cross-fertilization and cleistogmous only adapt to self-fertilization. It is shown that this genetic system is unprofitable to the populations of cleistogamous of which the two types of flowers exist on the different plants, which finally will lead to completely homo-zygous and become a single biotype consisting of genetically similar individuals. For the species of the two types of flo-wer, on the same individual plant, the genetic system may be better than above one, because such plants not only produce a great many seeds which are the result of self-fertilization, but may also form a favourable gene combination following inter-racial hybridization of chasmogamous. But the author found that interracial hybridization in chasmogamous of S. oligophyl-la appears difficult because of the arachnoid haris on surface of their anthers, which alaways adhere to the branchlets of the style, so the self-fertilization is compelled to facilitate. It is shown that there are some shortages in the chasmogamous of S. oligophylla.
    TAXA NOVA MAGNOLIACEARUM
    Law Yuh-wu
    1985, 5(3):  121-131. 
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    NEW TAXA OF THE GENUS HEDYSARUN L.IN CHINA
    Shue Long-zhan
    1985, 5(3):  133-140. 
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    THE GENUS GYMNASTER KITAM.OF CHINA
    Fu Jing-qiou
    1985, 5(3):  141-146. 
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    THE TAXONOMY OF DRYOATHYRIUM CHING IN CHINA
    Hsieh Yin-tang
    1985, 5(3):  147-157. 
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    Dryoathyrium is a small genus of the Athyriaceae, it was frist founded by Ching in 1941, but some pteridologists (such as Tard.-Blot 1958, Tagawa 1959, S. Kurata 1961, Copeland 1974 and others) did not agree with Ching's treating (as a distinct genus). On the other hand, in 1958, Holttum also basing on the same species founded the genus Parathyrium, which was obviously synonym of Dryoathyrium. It occured ainly because of the world war Ⅱ and the turmoil after the war which hindered the science and culture exchange of the world. The rich materials studied by auther recently prove that Dryoathyrium can be a distinct genus, acording to both the morphological characteristics and geographical distribution. Drgoathyrium contains about 20 species in the whole world.13 species have been known in China so far. Drgoathyrium is mainly distributed in temperate and subtroΞ pical zones of eastern hemisphere. But most of them mainly distribute in China. The present paper gives a description of the genus, a key to the species of China and a summary account of distributioncon dition of the species in China.
    A NEW SPECIES OF GENUS SERIPHIDIUM(BESS.)POLJAK.FROM CHINA
    Ling Yeou-ruenn
    1985, 5(3):  159-161. 
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    A NEW SPECIES OF DRACOCEPHALUM FROM XINJIANG
    Liu Guo-jun
    1985, 5(3):  163-165. 
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    A NEW SPECIES OF THE GENUS PYROLA FROM XINJIANG
    Yang Chang-you
    1985, 5(3):  167-169. 
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