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1988, Vol.26, No.3 Previous Issue    Next Issue
Taxonomic Study on Polygonatum odoratum Complex
Wang Jin-Wu, Yang Ji, Li Mao-Xue
1988, 26 (3): 165-172. 
Abstract ( 0 )
This paper deals with the morphological and cytological variation in various forms
of P. odoratum complex.  A quantitative analysis on the correlation between some diagnostic
characteristics was also made with pictorialized scatter diagram and histogram.   The results
show that the presence or absence of angles on stems is closely correlated  with  smooth  or
verrucate lower surface of leaves and the position of stamens (above or below the middle). With
chromosome numbers, they heve 2n=18 and 2n=20 respectively.  It is suggested to treat them
as two distinct species and restore P. simizui Kitag as species status.
The Genus Herminium Guett. (Orchidaceae) in China
Lang Kai-Yung
1988, 26 (3): 173-188. 
Abstract ( 0 )
Herminium is a genus of about 26 species, mainly distributed in the temperate and
subtropical regions of Asia and Europe.  Yunnan, Sichuan and Xizang in China are the pre-
sent distribution centre as well as differentiation centre of the genus. In the present paper, taxa
of Herminium hitherto recorded in China are taxonomically and phytogeographically discussed
and revised, and, as a result, 18 species are recongnized, including two newly recorded spe-
cies, H. angustilabre King et Pantl. and H. quinquelobum King et Pantl., and 12 species en-
demic to China.  A full list of synonyms is given, a key to the species is provided and the
distribution areas of all taxa are mapped.
On Distributional Features of the Genus Aconitum in Sino-Himalayan Flora
Li Liang-Qian
1988, 26 (3): 189-204. 
Abstract ( 0 )
The geographical distribution of Aconitum in the  Sino-Himalayan  subregion  is
analysed in the present paper on the basis of taxonomy and relationship between the infrage-
neric taxa.  Asaresult, some conclusions may be arrived as follows:
     1.  The Sino-Himalayan subregion is the frequency centre and the diversity centre of the
genus.  For analysis, the distribution area of the genus are assigned to three floristic regions,
viz. 1) the East-Asian floristic region, consisting of the Sino-Himalayan subregion and Sino-
Japanese subregion, 2) the Euro-Siberian region and 3) the North-American region (Table 1).
In the East-Asian floristic region, the Sino-Himalayan subregion comprises 3 subgenera, about
5 sections, about 13 series and nearly 180 species.  However, the Sino-Japanese subregion has
only 2 subgenera, 2 sections. 6 series and about 50 species.  The Euro-Siberian region has 2
subgenera, 2 sections, about 9 series and nearly 70 species.  The North-American region has
2 subgenera (one of the 2 subgenera has only 1 species), 1 section, 1-2 series and about 26
species.  Obviously, the Sino-Himalayan subregion is the richest in taxa.
      2.  The Sino-Himalayan subregion is not only the preservation centre of the primitive
 groups and species, but also an actively differentiating region.  Largely in the Sino-Himalayan
subregion occurs primitive or more primitive tava in the genus, such as Sect. Fletcherum, Sect.
 Alatosperum and Sect.  Sinaconitum, Ser.  Tangutica and Ser. Brunnea etc.: A fletcherianum,
 A. novoluridum, A. chrysotricum, A. brevicalcaratum, A. polycarpus, A. nagarum, A. tanguti-
 cum, A. hookeri, A. naviculare, A. violaceum, etc.  On the other hand, the Sino-Himalayan
 subregion also has the most or relatively advanced taxa, represented by the annual monotypic
 subgenus Gymnaconitum, A. spiripetalum, A. hamatipetalum and A. bulbitiferum ect.  About
 50 infraspecific taxa occur in the subregion.  For example, A. hemsleyanum has 8 varities, A.
 franchetii has varities and A. nagarum 1 varity and 2 forms, ect.
       3.  In the region under discussion the genus  Aconitum  shows  remarkable  endemism.
 The endemic taxa include 3 sections (Sect. Fletcherum, Sect.  Alatosperum and Sect.  Sina-
 conitum), 3 series (Ser. Brevicalcarata, Ser. Crassiflora and Ser. Bullatifolia) and nearly 150
  species, among which primitive and advanced ones are both present.
       4.  The pattern of geographical distribution of the genus Aconitum shows remarkable
  relationship between latitude and altitude.  The majority of species of this genus prefer habi-
  tats with a cool and more or less constantly moist climate.  In the Sino-Japanese subregion, with
  a higher latitude, the genus has an altitude range of 500-1500 m, whereas in the Sino-Hima-
  layan subregion the range is 2900-5000 m.
        To sum up, the Sino-Himalayan subregion is the diversity centre, the frequency centre, the
differentiation centre, the preservation centre of the primitive taxa and the centre of endemism
of the genus Aconitum, and its development in this subregion has probably been accelerated
by the lift of the Himalayas and the complicated environmental conditions.
Chemotaxonomic Relationship Between Murraya and Merrillia (Rutaceae)
But Paul Pui-Hay, Kong Yun-Cheung, Li Qian, Chang Hong-Ta, Chang Kiaw-Lan, Wong Khoon-Meng, Gray Alex,er I., Waterman Peter G.
1988, 26 (3): 205-210. 
Abstract ( 0 )
 Swingle[14-15] divided Aurantioideac into two tribes, one of which, Clausereae was
further divided into three subtribes, namely, Micromelinae, Clauseninae and Merrilliinae. Mic-
 
romelinae and Merrilliinae each have one genus, whereas Clauseninae has three genera.  Mor-
phologically, the Clauseneae is a natural tribe, the five genera are related in a linear sequence,
starting with Micromelum as the most primitive and progressing  in  sequence to Glycosmis,
Clausena, Murraya and Merrillia.  Chemical studies also support this linear relationship, as
revealed by the degree of oxygenation and complexity of the 3-methyl carbazole  alkaloids,
from CH3 and C13 in Glycosmis to CHO and C18 in Clausena and COOH and C23 in Mur-
raya[20-21].  Distribution of flavonoids also indicates  the  progression  from  Clauseninae  to
Merrilliinae[18-19].
      Extensive work has been conducted on the chemistry and taxonomy of the genus Mur-
raya [1,5,7-13,16],  and the data from these studies clearly indicate the presence of two distinct
groups.  Based on a combination of morphological and chemical differences, we agreed with
Tanaka[16-17] in dividing Murraya into two sections, i.e. section Murraya and section Ber-
gera[1].
      However, our previous study[1] has not touched on the relationship between the two sections.
Tanaka[16-17] placed section Bergera before section Murraya, and indicated that the former is
close to Micromelum and the latter to Merrillia.  Swingle[14-15], on the other hand, put taxa of
section Murraya ahead of those of section Bergera, presumably suggesting that plants of sec-
tion Murraya are more primitive than those of section Bergera, this arrangement was followed
by Huang[2-3].   The two conflicting viewpoints would have direct bearings on the interpreta-
tion of the trends of biogenesis of prenylated indole and carbazole alkaloids, as well as on the
weighing of the relative advancement of the morphological characters within the genus, such
as in the assignment of indices of divergence and in the construction of Wagner Divergence
Diagrams. Without more objective criteria, we find it difficult to select one of the two systems.
     In order to determine the relationship between the two sections of Murraya, we decided
to study plants of related genera, with the hope that the chemical data may shed light on the
problem.  A plant that attracted our attention is Merrillia caloxylon (Ridley) Swingle.  So far,
only eupatorin and a few other flavonoids have been reported from the fruit of this species[4,6].
     Although Me. caloxylon belongs to Merrilliinae, a subtribe next to Clauseninae, Tanaka[16-17]
believes that it is close to Murraya section Murraya.  Swingle[15], also suggested that this species
might have developed from the same stock that gave rise to Mu. paniculata.   If their inter-
pretations were accurate, we would expect that Me. caloxylon would also contain yuehchukene
and 8-prenylated coumarins.   The presence of the antiimplantation agent would not only open
up a new source of the compound but also help us judge the relationship between the two sec-
tions of Murraya.  It is in this context that we studied the chemical composition of Me. calo-
xylon.
     Indeed, root and stem bark of Me. caloxylon were found to contain the antiimplanta-
tion indole alkaloid yuehchukene (1), and the 8-prenylated coumarins sibiricin (II) and phe-
balosin (III), as well as 3-(3-methy1-buta-1,3-diene) indole (IV) and eupatorin (V.) Details
on the chemical profiles are reported in another paper.
     Through this exercise, we have confirmed the close relationship between Merrilliinae and
Murraya section Murraya, plants of both taxa contain yuehchukene and 8-prenylated coumarins,
but no carbazole alkaloid.  Root and stem bark of Me. caloxylon, like those of plants of section
Murraya, are strawcolored to pale whitish.  Its leaves also bear wings along the rachis an in
Mu. alata, and the seeds are also villous.  However, Me. caloxylon has long trumpetshaped flo-
wers 55-60 mm long, much larger than those found in other rutaceous plants. Its fruit is ob-
 
long, up to 11 cm long and 8 cm across, bearing a thick and warty pericarp, exuding a very stick
mucilage when cut, and containing numerous seeds (>30).  The plant was known to exist in
the Malay Peninsula and north Sumatra[15], but, according to David Jones (per. comm.) of
the University of Malaya, is now only available in cultivation in Malaysia and Singapore, a li-
mitation to any further exploitation as an additional source of yuehchukene.
      Besides confirming the close relationship between Merrillia and section Murraya, we may
also conclude that section Bergera is close to Glycosmis and Clausena, since they are known
to contain carbazole alkaloids but no yuehchukene.  Accordingly, we find Tanaka’s arrange-
ment more acceptable: plants of section Bergera are more primitive than those of section Mur-
raya, the former is close to Clausena whereas the latter (notably Mu. alata) to Merrillia.  The
relationship among the gonera with in Clauseneae may be illustrated as follow: Micromelum→
Glycosmis→Clausena→Murraya sect. Bergera→Murraya sect. Murraya→Marrillia.
      Accordingly, we may decide that the following character states are more primitive am-
ong plants of Murraya and Merrillia: root and stem bark dark brown, leaf rachis wingless,
flower small, fruit purple-black with few seeds, and seed coat glabrous.   In contrast, straw-
colored or pale whitish bark, winged leaf rachis, large flower, red or yellow fruit with many
seeds and villous seed coat can be regarded as more advanced characters.
Acknowledgments    Partial support was received from  the  World  Health  Organiz-
ation Special Programme on Human Reproduction and the Kevin Hsu Research Fund (to YCK)
and Commonwealth Science Council (to PPHB).  The staff of the Singapore Botanic Gardens
and the Forest Research Institute of Malaysia are thanked for their assistance in collecting plant
material.
Monocladus, Genus Novum Bambusoidearum (Poaceae)
Chia Liang-Chi, Fung Hok-Lam, Yang Ya-Ling
1988, 26 (3): 211-216. 
Abstract ( 0 )
Setiacis—A New Genus of Grasses
Chen Shou-Liang, Jin Yue-Xing
1988, 26 (3): 217-223. 
Abstract ( 0 )
Our observations on characters of leaf epidermis, lemma, palea etc. in the genera
Acroceras Stapf (many species), Neohusnotia tonkinensis (Balansa) A. Camus (the type of
Neohusnotia), Setiacis diffusa (Chia) S. L. Chen & Y. X. Jin (the type of Setiacis), Lasiacis
divaricata (L.) Hitchc. (the type of Lasiacis[4]) and Psilochloa pilgerana (Schweick.) Launert
(the type of Psilochloa[4]) in Subtribe Paspalinae[1] Keng& Keng f. show that Setiacis diffusa
differs from the others by several characters, which merits establishing a new genus—Setiacis
S. L. Chen & Y. X. Jin in this subtribe[1].  The Latin description of the new genus is given
in this paper.
New Taxa of Bambusoideae from Guangdong
Lin Wan-Tao
1988, 26 (3): 224-234. 
Abstract ( 0 )
New Discoveries of the Genus Hippophae L. (Elaeagnaceae)
Lian Yong-Shan
1988, 26 (3): 235-237. 
Abstract ( 0 )
This  paper  represents  new  discoveries  of  the  genus  Hippophae  L,  inclu-
ding two new sections: i. e. Sect. I. Hippophae and Sect.  II.  Gyantsenses Lian, a new rank
species H. gyantsensis (Rousi) Lian, as well as a new record of H. rhamnoides L. subsp. tur-
kestanica Rousi in Gansu.  Besides, a key to the sections and species is provided and an account
of the new classification scheme on the genus is given.
New Taxa of Orchidaceae from China (3)
Chen Sing-Chi
1988, 26 (3): 238-240. 
Abstract ( 0 )
Chromosome Numbers of 10 Species and 3 Varieties in Actinidia Lindl.
Xiong Zhi-Ting, Huang Ren-Huang
1988, 26 (3): 245-247. 
Abstract ( 0 )
Somatic chromosome numbers of 10 species and 3 varieties in  Actinidia
Lindl. are reported for the first time, except A. polygama (Sieb. et Zucc.) Maxim. Two
ploidy levels, diploid and tetraploid, are found both in A. polygama and A. kolomikta (Ma-
xim. et Rupr.) Maxim. Chromosome numbers are listed as follows: A. kolomikta (Maxim. et
Rupr.) Maxim. 2n=58, 116, A. polygama (Sieb. et Zucc. Maxim. 2n=58, 116, A. macrosper-
ma Liang 2n=116, A. callosa var. henryi Maxim. 2n=116, A. callosa var. discoler Liang 2n
=116, A. cylindrica Liang 2n=58, A. chrysantha Liang 2n=116, A. sabiaefolia Dunn 2n=
58, A. melliana Hand.-Mazz. 2n=58, A. hemsleyana Dunn 2n=58, A. fulvicoma var. lanata
(Hemsl.) Liang 2n=58, A. latifolia (Gardn. et Champ.) Merr. 2n=58, and A. lanceolata
Dunn 2n=58.