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1991, Vol.29, No.3 Previous Issue    Next Issue
A Taxonomic Study on the Genus Polygala L. in China
Chen Shu-Kun
1991, 29 (3): 193-229. 
Abstract ( 0 )
The present paper deals with the history of taxonomy, groos morphology, pollen
 morphology, distribution, system and taxonomic treatment of the genus Polygala L. from
 China. Three subgenera, 4 sections, 41 species and 8 varieties are recognized in this
 treatment, of which 2 sections are described as new.
      The system of Chinese species of Polygala L. is proposed as follow:
      Subgen. 1. Chamaebuxus (DC.)Duchartre (Typus: Polygala chamaebuxus L.)
      Sect. 1. Arillus S. K. Chen, sect. nov. (Typus: Polygala arillata Buch.-Ham. ex D. Don).
This section consists of about 20 species, distributed in the tropics and subtropics of Asia and
Africa, with 7 species found in South China.
      Subgen. 2. Pseudosemeiocardium (Adema) J. Chetek et B. Krisa( Typus: Polygala
furcata Royle).
      Sect. 1. Villososperma C. Y. Wu et S. K. Chen (Typus: Polygala wattersii Hance ). There
are 3 species in this section, distributed in S. China and N. Vietnam.
      Sect. 2. Saxicola S. K. Chen, sect.nov. (Typus: Polygala saxicola Dunn). This section
consists of 8 species, among which P. tricornis Gagnep. and P. saxicola Dunn are distrib-
uted in both Vietnam and China, and the other 6 species are endemic to China.
     Sect. 3. Pseudosemeiocardium ( Typus: Polygala furcata Royle). This section consists
of about 7 species, distributed in SW China, extending from Indo-China Peninsula, south-
ward to Malay, the Philippines, Indonesia and New Guinea, westward to the southern slope
of the Himalayas and N. India, northward to Japan.
     Subgen. 3.  Polygala (Typus: Polygala vulgaris L. ).
     400 species or more belong to this cosmopolitan subgenus. Most species are found in
America and Africa, with 18 species discovered in China.
     Taxonomic evidence: The characters of flowers, fruits and seeds, the indumentum of
seeds and presence or absence of caruncles are stable and also correlated with one
another. There is a certain combination of the above-mentioned characters in a given
group, which provide reliable evidence for the infrageneric division. A good example is the
Polygala arillata group, grown under the tropical and subtropical forests, which has large,
yellow flowers, with sepals fallen after blossom. The flower has carinas with a cristate appen-
dix, which is of 2-9 long narrow pieces. The seeds are spherical, with a hooded caruncle. Its
fruits are of annuloid stripes. (Fig. 1). The Polygala tenuifolia Willd. group, cosmopolitan
in distribution, has a middle-sized, purple or yellow flower with persistent sepals. Cristate
appendix of carina is usually fimbricate. The seed in the group is oblong or subovoid, with a
trilobate caruncle. Carpels of the fruits of this group are without annuloid stripes(Fig. 3).
The third group, Polygala saxicola group, is between the two as indicated above. The group
has a small, yellow or occasionally purplecolored flower, with sepals fallen after blossom or
sometimes with a persistent outer sepal. The cristate appendix of carina is lamellar or
cucullate. The seed of the group is sometimes with pubescences and hooded caruncles some-
times with hirtoselike villoses and no caruncle (Fig. 2)
      pollen morphology and systematic treatments:
      The pollen morphology of the domestic Polygala seems to support division of Polygala
 L. into three groups as follows: A. Pollen grains subspheroidal, 10-19-colpate, colpi usual-
 ly rather wide, relatively psilate in the polar area; B. Pollen grains reniform, 22-26-colpate,
 sculptural in the polar area; C. Pollen grains long-spheroidal or subspheroidal, 9-
 23-colpate, with long and deep colpi, which usually extend to the relatively psilate polar
 area. The pollen morphology is naturally correlated with the morphology of flowers, fruits
 and seeds.  Based on these, three subgenera and four sections no subdivision in
 Subgen. Polygala)are recognized.
A Preliminary Study on the Polyploid Series and Cytogeography of Najas graminea
You Jun, Sun Xiang-Zhong, Wang Hui-Qin
1991, 29 (3): 230-234. 
Abstract ( 0 )
Najas graminea is first reported to have a population of 2n = 12. A cytogeographic
survey of this species reveals that the diploid (2n= 12) population is so far only found in
Yunnan (You Jun 8804, in Herb. WH) and its adaptive radiation has probably resulted in the
distribution pattern of N. graminea today in Asia. The polyploids are more widely distributed
than the diploid, but no correlation was found between polyploids and geographic distribu-
tion, soil or climate types. The comparison of the karyotypes between diploid and hexaploid,
lack of inter-specific hybridization in nature, and the occurrence of semi-cryptic polyploids
in the populations suggest that polyploids of N. graminea are the result of autopolyploidy (at
least in China). The highest polyploidy (almost 17X), the most asymmetrical karyotype, and
the most reduced floral structure (the spathe is absent) support the suggestion that the
N. graminea be the most advanced taxon in Najas.
Pollen Morphology of the Genus Ligusticum from China and Its Systematic Significance
Wang Ping-Li, Pu Fa-Ting, Ma Jian-Sheng
1991, 29 (3): 235-245. 
Abstract ( 0 )
The genus Ligusticum (Umbelliferae)consists of over 60 specics. So far found are
34 species in China. In the present paper pollen morphology of 25 species of Ligusticum were
investigated. Among them only L.scothicum L.is not distributed in China, but in the Soviet
Union, Korea, Japan and North America. Pollen grains of all the species were examined by
LM, SEM and four species examined under TEM. Seventeen species are palynologically re-
ported here for the first time.
     Based on our observation and data from other authors the shape of pollen grains
in Ligusticum may be divided into four types: (1)Rhomboidal, P/E 1.14-1.87; colpi slen-
der; pores goniotreme, rectangular, protruding; exine 2-layered, nearly equal in thickness,
columellae inaistinct, sculpture reticulate or obscure under LM, psilate and finely rugulate
under SEM ( including L. franchetii; L. tachiroei and L. sikiangensis); (2) Ellipsoidal,
P/ E 1.72-2.25; colpi slender, rarely syncolpate; pores pleurotreme, rarely goniotreme,
subrectangular; exine 2-layered, nearly equal in thickness, columellae distinct, sculpture
reticulate, distinct or indistinct under LM, rugulate or brevistriate-reticulate under SEM (in-
cluding L. brachylobum; L.pteridophyllum); (3) Rectangular, P/E 1.71-2.42; colpi long,
rather long or wide and short; pores pleurotreme, rounded, subrounded or lalongate; exine
2-layered, sexine thicker than nexine; columellae distinct, sculpture reticulate distinct or ob-
scure under LM, rugulate, brevistriate or striate-reticulate under SEM ( L. angelicifolium
L. capillaceum; L. multivittatum; L. sinense ; L. sinense cv. Chuanxiong ; L. sinense cv. Fuxiong ;
L. jeholense; L. involucratum; L. oliverianum; L. scothicum; L. scapiforme; L. hispidum;
L. daucoides; (4) Equatorial-constricted, P/E 2.00-2.42; colpi short or rather short; pores
rounded, ellipsoidal or lalongate; exine 2-layered, sexine thicker than nexine, columellae dis-
tinct, sculpture distinctly reticulate under LM, rugulate, brevistriate or striate-reticulate undr
SEM (L.filifolium; L. discolor; L. ajaense; L. acuminatum)
     The revolutionary trends of pollen types are as follows: rhomboidal→ ellipsoidal;
rhomboidal→ lalongate-rhomboidal→ rectangular→ equatorial-constricted. The aperture is
of two types i.e.goniotreme and pleurotreme.
     Regel (1858)treated Tilingia as an independent genus and Leute (1969)separated the
genus Ligusticpsis from Ligusticum, but pollen information supports K.-Pol. (1916) and
Hiroe's (1979)systematic arrangement, placing Tilingia and Ligusticopsis into Ligusticum,
because Tilingia and Ligusticopsis are  similar  to Ligusticum in  pollen  morphology:
tricolporate, exine 2-layered, columellae usually distinct and sculpture reticulate.
A Study on Pollen Morphology of Some Chinese Genera in Tribe Anthemideae
Chen Song-Bo, Zhang Jin-Tan (Chang King Tang)
1991, 29 (3): 246-251. 
Abstract ( 0 )
This paper deals with pollen grains of 9 chinese genera of Trib. Anthemideae
Cass., which include the genera: Ajania Poljak., Hippolytia Poljak., Stilpnolepis Krasch.,
Elachanthemum Ling et Y. R. Ling, Filifolium Kitam., Ajaniopsis Shih, Kaschgaria Poljak.,
Neopallasia Poljak., Seriphidium Poljak.,
     Pollen grains of these genera are isopolar, radially symmetrical, 3-colporate, NPC 345,
spheroidal, sometimes suboblate or subprolate. Polar axis 20.0-30.0μm equatorial axis 20.0
-30.0μm. The exine consists of three layers: tectum, columellae and nexine. Exine thickness
3.2-5.6μm, usually the columellae is the thickest.
     According to the differences of exine ornamentation, they are divided into two main
groups: 1. with distinct spines, including the genera Ajania Poljak., Hippolytia Poljak.,
Stilpnolepis Krasch., 2.with indistinct spinules, including the genera Elachanthemum Ling et
Y.R.Ling,   Filifolium Kitam.,   Ajaniopsis Shih,   Kaschgaria.,   Neopallasia Poljak.,
Seriphidium Poljak.
Seed Morphology of Impatiens L. (Balsaminaceae) and Its Taxonomic Significance
Lu Ying-Qing, Chen Yi-Ling
1991, 29 (3): 252-257. 
Abstract ( 0 )
The seed surface of 12 species of Impatiens L. from Mt. Omei was observed under
SEM for the first time. The important characters used in the paper include cell specialization
on seed surface, arrangement pattern of the cells, the degree of the cell elevation, chalazal
zone morphology and appendix at the tail of the seed. According to these characters, the seed
surface morphology of 12 species can be divided into two types: 1. the seed without conspicu-
ous differentiation of surface cells, laevigate on the surface, represented by I. wilsoni; the
seeds of species indicated by 3-colpate pollen grains are expected to belong to the type. 2. the
seed with the large cell elevation at different levels, surface scabrous, represented by the other
11 species; most species with 4-colpate pollen have this kind of seeds. The results verify that
the seed morphology of the genus can supply characters significant to taxonomy of the genus
at species level. The evolution of seed surface of Impatiens has close correlation with that of
the flower and pollen morphology.
A Taxometric Analysis of Characters of Polygonum lapathifolium L.
Yang Ji, Wang Jin-Wu
1991, 29 (3): 258-263. 
Abstract ( 0 )
 Polygonum lapathifolium L. is a morphologically variable and taxonomically com-
plicated group. The height of plants and the degree of nodal expansion greatly vary in differ-
ent habitats. In this work field observation and mass collection in different habitats of this
species were made. By means of biometric techniques, principal component analysis,
discriminant analysis, scatter diagram and histogram, supplemented by transplantation ex-
periment, it is revealed that the height of plants and the degree of nodal expansion of P.
lapathifolium are evidently affected by environmental conditions, and these two variables are
not correlated with, but independent from, each other. The results also show that the
indumentum on the lower leaf surface is not constant. Therefore all the characters are not re-
liable diagnostic ones and any taxonomic treatment based on these characters is not reasona-
ble. In this paper, P. nodosum Pers. is reduced as a synonym of P. lapathifolium L. and P.
lapathifolium var. salicifolium Sibth. is also eliminated.
New Taxa of Morus (Moraceae) from China
Cao Zi-Yu
1991, 29 (3): 264-267. 
Abstract ( 0 )
Three New species and one new variety of the genus Morus (Moraceae) are des-
cribed from China. They are Morus gongshanensis, M. hastifolia, M. trilobata, M. mongolica
var. longicaudata.
A New Species of Rhododendron from Hunan
Liu Qi-Xian, Zhang Can-Ming
1991, 29 (3): 270-271. 
Abstract ( 0 )
 Rhododendron shimenense Q. X. Liu et C. M. Zhang (Ericaceae) is described as
new from Hunan Province, China.
A New Species of Genus Astragalus L. from Nei Mongol
Jiang Zhi-Gang, Yin Zu-Tang
1991, 29 (3): 272-273. 
Abstract ( 0 )
In this paper one new species of the genus Astragalus L. (Papilionaceae) is des-
cribed from Nei Monggol, China. It is A. daqingshanicus Z. G. Jiang et Z. T. Yin.
A New Species of Bambusoideae from Yunnan
Xue Jia-Rong
1991, 29 (3): 274-275. 
Abstract ( 0 )
A new species of the genus Neosinocalamus Keng f., N. yunnanensis, is described in this paper.
Additional Description of Callianthemum cuneilobum Hand.-Mazz. from Shanxi
Yu Xiang-Yun, Li Ben-Lang, Li Yu-Mei
1991, 29 (3): 276-277. 
Abstract ( 0 )
An additional description of Callianthemum cuneilobum Hand.-Mazz. is pres-
ented in this paper with a new collection with flowers. Because of lacking adequate specimens
the species was treated as a synonym of C. farreri W. W. Smith in Fl. Reip. Pop. Sin. 28:
245, 1980.
Some New Taxa of Chara from Northwest China
Zhao Qing-Fang
1991, 29 (3): 278-282. 
Abstract ( 0 )
In this paper, two new species and one new record of the Chara from northwestern
China are reported. They are Chara lanzhouensis Q. F. Zhao, C. pseudoglobularis Han, C.
arcuatifolia Vilhelm.
Parsimony, Character-Polarization and Median Elimination Series—A Dissentation from Dr. Li
Zhang Dian-Xiang
1991, 29 (3): 283-287. 
Abstract ( 0 )
 The Median Elimination Series method differs from those of other cladists both
theoretically and technically. The principle of parsimony is one of the bases of scientific
hypotheses; the theory of evolution is the causal explanation relationships between
organisms. Both of them are the bases of cladistics. Thus it is implausible to replace the for-
mer by the latter.
     Distinguishing a plesiomorphy from a reversion and a direct apomorphy from a cyclic
apomorphy as indicated by Dr Li (1990) in his character 5 and character ll, is difficult if not
impossible. So the basis of MES is vulnerable.
     Using only 2 taxa in calculating the value of media and thus deciding the placement of a
taxon in a cladogram would bring uncertainties when reversion exists.
     Morphological character homoplasy and reversion must be treated equally if Wagner's
parsimony principle is followed. But reversion is ignored in MES calculation.
     Several more parsimonious cladograms are yielded with Dr Li's data when Farris's
method is followed.
     MES is not a better alternative anyway.