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1994, Vol.32, No.5 Previous Issue    Next Issue
An Analysis of the Flora of Qinling Mountain Range: Its Nature, Characteristics, and Origins
Ying Tsun-shen
1994, 32 (5): 389-410. 
Abstract ( 0 )
The Qinling Mountain Range, which covers an area of ca. 76500km2 and ranges
 from 32°05′ to 34°45′ N and from 104°30′ to 115°52′ E, is a major watershed of the
 Huanghe and Chang jiang rivers with the highest peak about 3767 m above sea level. The
 flora comprises ca. 3124 species in 892 genera, of which 51.9% of species and 4.4% of the
 genera are endemic to China. Evoluated in this paper is the importance of the 20 larger fami-
 lies which together contain 65.2% of the total number of species. The phytogeographical
 affinities of genera of seed plants in the flora are analyzed and briefly discussed. Among the
 native genera of the flora of the Qinling Mountain Range, 220 (26.8%) are tropical, 563
  (68.5%) temperate, and 39 (4.7%) endemic to China. It is clear from the figures that
 temperate genera play an important role in the flora and vegetation of the Qinling Mountain
 Range. The features of the flora include the unusually high proportion of endemic species, a
 wealth of Sino-Japanese elements and prominant temperate nature in compsition. On the ba-
 sis of analysis of paleobotanical materials in the Qinling Mountain Range and adjacent areas,
 historical distribution of dominant species, and the origin and relationships of Chinese en-
 demic genera occurring there, the flora is of outstanding originality. No doubt, the rich and
 diverse flora have evolved gradually and autochthonously at least since the latest Cretaceous.
New Chromosome Counts of Some Dicots in the Sino-Japanese Region and Their Systematics and Evolutionary Significance
Hsu Ping-sheng, Weng Ruo-feng, Siro Kurita
1994, 32 (5): 411-418. 
Abstract ( 0 )
 New somatic chromosome numbers for nine species eight families and eight gen
era in the Sino-Japanese Region are reported here as shown in Table 1. Data of six genera
are previously unknown cytologically. The bearings of these new data on the systematics
and evolution of the related species, genera or families are discussed as follows: (1) Platy-
carya strobilacea Sieb. et Zucc. (Juglandaceae). The chromosome number of this species is
2n=24, with a basic number of x=12, which deviates from 2n=32 occurred in Juglans,
Carya, Pterocarya and Engelhardtia with the basic number x= 16. The Juglandaceae ap-
pears to be fundamentally paleotetraploid, with an original basic number of x = 6 in Platy-
carya and x-8 in the other four genera, although secondary polyploidy occurs in Carya.
Based on the remarkable morphological differences between Platycarya and the rest seven
genera of the family, Manning (1978) established two subfamilies: Platycaryoideae for
Platycarya and Juglandoideae for the other genera. Iljinskaya (1990), however, recently
established a new subfamily: Engelhardioideae for Engelhardtia. Lu (1982) points out that
because of a great number of primitive characters occurring in Platycarya, the genus could
not be derived from any other extant juglandaceous taxa but probably originated with the
other groups from a common extinct ancestor. The present cytological data gives support to
Manning′s treatment. We are also in favor of Lu′s supposition and suggest that basic aneu-
ploid changes, both ascending and descending, from a common ancestor with the original
basic number x=7, took place during the course of early evolution of the Juglandaceae and
led to the origin of taxa with x=6 and 8. Subsequent polyploidy based on these diploids oc-
curred and brought forth polyploids of relic nature today, whereas their diploid progenitors
apparently have become extinct. (2) Nanocnide pilosa Migo (Urticaceae). The chromo-
some number of this Chinese endemic is 2n-24, with a basic number of x=12. An aneu-
ploid series occurs in the Urticaceae, with x--13, 12, I1, 10, 9, 8, 7, etc. According to
Ehrendorfer (1976), x = 14, itself being of tetraploid origin, is the original basic number of
the whole Urticales, and descending aneuploid changes took place in the early stage of evolu-
tion of the Urticaceae and Cannabinaceae. In addition to Nanocnide, x= 12 also occurs in
Australina, Hesperonide and Lecanthus, and partly in Chamabainia, Elatostema, Girardinia,
Pouzolzia and Urtica. (3--4) Sedum sarmentosum Bunge and S. angustifolium Z. B. Hu
et X. L. Huang (Crassulaceae). The former is a member of the Sino-Japanese Region,
while the latter is only confined to eastern China. The chromosome number of Sedum is re-
markably complex with n=4-12, 14-16…74, etc. S. angustifolium with 2n=72 of the
present report is evidently a polyploid with a basic number of x =18 (9?) Previous and pre-
sent counts of S. sarmentosum show infraspecific aneupolyploidy: n = c. 36 (Uhl at al.
1972) and 2n=58 (the present report). These two species are sympatric in eastern China
and are morphologically very similar, yet distinguishable from each other (Hsu et al. 1983)
S. sarmentosum escaped from cultivation in the United States gardens exhibited high irregu-
larity in meiosis (Uhl et al. 1972). Uhl (pets. comm. ) suspected strongly that it is a high-
ly sterile hybrid. R. T. Clausen (pets. comm.) found that plants of S. sarmentosum natu-
ralized in the American Gardens propagated by means of their long stolons and broken stem
tips, and could not yield viable seeds. Hsu et al. (1983) found that some of the plants of S.
sarmentosum and S. angustifolium did yield a few seeds, but other did not. These species
are, therefore, by the large vegetatively apomictic. (5) Glochidion puberum (L. ) Hutch.
(Euphorbiaceae). The genus Glochidion includes about 300 species, but only eigth species
from the Himalayas have been studied cytologically, with n= 36 and 2n= 52, having a basic
number of x= 13. The present count for the Chinese endemic G. puberum establishes the
tetraploid chromosome number 2n= 64, and adds a new basic number x= 16 to the genus.
(6) Orixa japonica Thunb.  (Rutaceae). Orixa is a disjunct Sino-Japanese monotypic
genus. Out of the 158 genera of the Rutaceae, chromosome numbers of 65 genera have
hitherto been investigated, of which 42 genera are with x=9 (66.61%), some with x=7,
8 and 10, and rarely with x=13, 15, 17 and 19. The present count of 2n=34 for O.
japonica may have resulted from a dibasic tetraploidy of n=8+9. (7) Rhamnella frangu-
loides (Maxim.) Weberb. (Rhamnaceae). The chromosome number of this member of the
Sino-Japanese Region is 2n= 24. with a basic number of x= 12. The basic number x= 12
also occurs in Hovenia, Paliurus, Sageretia, Ceanothus and Berchemia. Hong (1990) sug-
gested that x= 12 in Rhamnaceae may be derived from descending aneuploidy of a paleote-
traploid ancestor. (8) Sinojackia xylocarpa Hu (Styracaceae). The chromosome number of
this rare Chinese endemic is 2n= 24, with a basic number of x =12, which is identical with
that in Halesia and Pterostyrax, but deviates from that in Styrax (x=8). The basic num-
ber x=8 in the Styracaceae may be derived from the original basic number x=7 by ascend-
ing aneuploidy in the early stage of evolution of the family, and x=12 may be derived from
polyploidy. (9) Thyrocarpus glochidiatus Maxim. (Boraginaceae). The chromosome num-
ber of this Chinese endemic species is 2n=24, with a basic number of x=12. An extensive
aneuploid sequence of x = 4-12 occurs in the Boraginaceae, of which x = 8, 7 and 6 are the
most common. The basic number x=12 also occurs in Cynoglossum and Mertensia. It is evi-
dent that aneuploid changes, both descending and ascending, from an ancestor with x = 7,
have taken place in the primary phase of evolutionary diversification of the Boraginaceae,
and subsequent polyploidy has given rise to x=15, 17 and 19 in a few genera (e. g. Amsin-
skia and Heliotropium). The origin of x=12 is not certain. Either it be a result of ascending
aneuploidy, or a product of polyploidy on the basis of x = 6. The present authors are in favor
of the latter.
A Study on Karyotypes and Geographical Distribution of Angelica and Related Genera (Umbelliferae) in China
Pan Ze-hui, Zhuang Ti-de, Yao Xin-mei, Sheng Ning
1994, 32 (5): 419-424. 
Abstract ( 0 )
The present paper deals with the karyotype analysis of 12 species in Angelica and
three related genera-Czernaevia, Archangelica and Coelopleurum from China. Ten kary-
otypes are reported for the first time. The parameters of chromosomes of 12 species are given
in Table 1 and the karyotypes are shown in Plates 1, 2, 3. The karyotype formulae are as
follows: A. dailingensis Z. H. Pan & T. D. Zhuang 2n= 22= 20m+2sm (SAT); A. likian-
gensis Wolff 2n=22=18m+4sm; A. nitida Wolff 2n=22=14m+4sm+4sm (SAT); A.
silvestris L. 2n=22=16m+4sm (SAT) +2st (SAT) ; A. decursiva (Mig.) Fr. & Sav.
2n=22=16m+4sm+2sm (SAT); A. tsinlingensis K. T. Fu 2n=22=18m+4sm; A. a-
paensis Shan & Yuan 2n=22=14m+6sm+2st (SAT); A. oncosepala Hand. -Mazz. 2n=
4x=44=28m+12sm+4st; A. ternata Rgl. & Schmalh. 2n=22=10m+8sm (SAT)+
4st (SAT); Czernaevia laevigata Turcz. 2n=22=14m+6sm+2sm (SAT) ; Archangelica
brevicaulis (Rupr.) Rchb. 2n=22=8m+2m (SAT) +4sm+4sm (SAT) +4st; Coelopleu-
rum saxatile (Turcz.) Drude 2n=28 = 12m +6sm+10st. The karyotypes of all the species
belong to “2A” except those of A. dailingensis and Coelopleurum saxatile, which belong to
“lA” and “2B” respectively.  According to the karyotypic type and the presence or absence
of subterminal chromosomes, the karyotypes of 9 species reported in the present paper and
11 species previously reported can be divided into 3 groups.  The scatter diagram (Fig.  2)
shows the karyotypic evolution of Angelica and related genera Coelopleurum with n = 14 and
karyotypic type “2B” is distinct from the related genera.  Based on the fact that the kary-
otypes are not obviously different among Czernaevia, Archangelica and Angelica, Czernaevia
and Archangelica might botter be merged in Angelica as sections.
On the Systematic Significance of Floral Organogenesis in Saururaceae
Liang Han-xing
1994, 32 (5): 425-432. 
Abstract ( 0 )
 The sequence of organ initiation and the change in number and position of sta-
mens and carpels are compared among the four genera in the Saururaceae in this paper. Sev-
eral evolutionary trends of organogenesis are revealed and summarized as follows:
     The first trend is that the first appearance of stamens and carpels converts from the me-
dian sagittal ones to the lateral ones. In Saururus the median sagittal stamens and carpels all
appear first, while in Gymnotheca the median posterior stamen arises first, the lateral pair
second, the median anterior one third, and the lateral carpels appear first. In Anemopsis and
Houttuynia the lateral stamens have changed to arising first. The second trend is the conver-
sion of initiation of stamens and carpels from the median sagittal ones in pair as in Saururus
to singular, acompanied by delayed development in Gymnotheca and to final degeneration of
the anterior stamen and carpel in Anemopsis and Houttuynia.  The latter two genera have a
pair or only one stamen at the posterior position, but during early development there is a gap
as a trace of degenerating stamen at the anterior position.  Moreover, in Gymnotheca with
four carpels, a gap exists at the anterior position, which is the place of the delayed anterior
carpel; in the genera with three carpels, a gap is present at the anterior position in Anemop-
sis, but absent in Houttuynia. The other trends involve the change of the two lateral stamens
from separate initiation in Saururus to initiation from a common primordium in Gymnotheca
and Anemopsis and to reduction of one stamen in Houttuynia; the conversion of single poste-
rior stamen to a pair from a common primordium in Anemopsis; the change of initiation of
three carpels from separate primordia in Anemopsis to from a ring primordium in Houttuyni-
a. The facts seem to show that the genus Houttuynia is more advansed than Anemopsis. The
evolutionary trends of flowers in the Saururaceae can be explaned as the results of fusion, re-
duction and multiplication. The systematic relationships among the four genera were inferred
in a diagram.
A Study on the Genus Juncus Linn. from China
Wu Kuo-fang
1994, 32 (5): 433-466. 
Abstract ( 0 )
 Juncus Linn. is a cosmopolitan genus with about 240 species, widely distributed
in both hemispheres, but most abundant in the frigid and temperate zones.  In the present
paper, a revision of this genus in China is made, and a key to the species is provided. This
paper also presents a systematic arrangement of the genus Juncus Linn. from China, recog-
nizing six subgenera, 14 sections (includ. ten new), four series (includ. two new), 77
species (includ. 14 new), one subspecies (new) and ten varieties (includ. four new). They
are as follows:
Subgen. 1. Genuini Buchen.
      Sect. 1. Inflexi K. F. Wu, sect. nov.
      Sect. 2. Effusi (V. Krecz. et Gontsch. )K. F. Wu, stat. nov.
Subgen. 2. Pseudotenageia V. Krecz. et Gontsch.
      Sect.  1.  Kangpuenses K. F.  Wu, sect. nov.
      Sect. 2. Compressi (V. Krecz. et Gontsch. )K. F. Wu, stat. nov.
Sect. 3. Tenues (V. Krecz. etGontsch.)K. F. Wu, stat. nov.
Subgen. 3. Poiophylli Buchen.
      Sect.  1. Nigroviolacei K. F. Wu, sect. nov.
      Sect.  2. Bufonii (V. Krecz. et Gontsch. )K. F. Wu, stat. nov.
Subgen. 4. Graminifolii Buchen.
Subgen.  5. Septati Buchen.
      Sect. 1. Allioides K. F. Wu, sect. nov.
      Sect.  2.  Articulati K.  F.  Wu, sect.  nov.
           Ser. 1. Articulati V. Krecz. et Gontsch.
           Ser. 2. Dongchuanenses K. F. Wu, ser, nov.
Subgen.  6. Alpini Buchen.
     Sect.  1. Triglumes K. F. Wu, sect. nov.
           Ser.  1. Triglumes K. F. Wu, ser. nov.
           Ser. 2. Benghalenses K. F. Wu, ser. nov.
     Sect. 2. Minimi K. F. Wu, sect. nov.
     Sect.  3. Sikkimenses K. F. Wu, sect. nov.
     Sect. 4. Concinni K. F. Wu, sect. nov.
     Sect.  5. Sphacelati K. F. Wu, sect. nov.
Notulae De Ranunculaceis Sinensibus (XVII)
Wang Wen-tsai, Li Liang-qian
1994, 32 (5): 467-479. 
Abstract ( 0 )
One species and one variety of Aconitum and Delphinium each, one species of
Thalictrum, one subspecies of Adonis, and five species of Ranunculus are described as new.
The new finding of Thalictrum rotundifolium from southern Xizang is reported, and after
analysing the morphological characters of leaves, stamens, and carpels, this species is con-
sidered to be more or less related to T. scabrifolium, a species endemic to Yunnan.
Supplementary Description of Cycas multipinnata C. J. Chen et S. Y.Yang
Chen Chia-jui, Yang Si-yuan
1994, 32 (5): 480-481. 
Abstract ( 0 )
A detailed description of a remarkable species of Cycas, C. multipinnata C. J.
Chen et S. Y. Yang from S. Yunnan of China, is given.
New Taxa of Potentilla from North China
Zhang Yong, Yin Zu-tang
1994, 32 (5): 482-483. 
Abstract ( 0 )
An Examination on Indumentum and Fruit of Dimocarpus longan and D. confines
Fu De-zhi, Song Shu-yin
1994, 32 (5): 484-487. 
Abstract ( 0 )
Examination on hairs and fruits of the Dimocarpus longan Lour.  (Guiyuan) and
D. confinis (How et Ho) H. S. Lo (magic fruit) was carried out. The fruit of D. longan
was found to be of smoothly colliculate or granulate protuberances and typical tuft hairs on
the surface, and the leaf was also of tuft hairs on the lower surface. However, the fruit of
D. confinis was of dense and hard aculeate protuberances and simple and glandular hairs on
the surface, and the leaf was also of the same kind of hairs on the lower surface. These char-
acteristics of D. longan can been easily detected in samples of commercial fruits, which were
misidentified as the fruits of D. confinis. Moreover, the fruit surface of Guiyuan Sampled
from the markets had no any artificially destroryed trace, which indicated that they were
not forged through the processing of the fruits of D. confinis, and thus they were true
Guiyuan, the fruit of D.  longan.