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1992, Vol.30, No.4 Previous Issue    Next Issue
Systematic Study on Lomatogonium A. Br. (Gentianaceae)
Liu Shang-Wu, Ho Ting-Nung
1992, 30 (4): 289-319. 
Abstract ( 0 )
The present paper deals with the infrageneric classification, phylogeny and geographic distribution of the genus Lomatogonium.
    A cladistic analysis was undertaken to establish the taxa and to evaluate the relationships between the taxa. The PAUP computer program was used in this analysis. The most parsimonious tree (Cladogram) of the rotate-corolla group of
subtribe Gentianinae shows that Lomatogonium is closely related to Lomatogoniopsis and Swertia, but distantly to Veratrilla. Among them, Swertia is more primitive  than Lomatogonium and hence Sect. Swertia was selected as the outgroup to polarize the character states of ingroup (Lomatogonium). A data matrix of 29 charaters of Lomatogonium was made for constructing the cladogram. Two most parsimonious trees were formed one of which, with the lowest f value, was at last selected as a shortest tree. In this tree 18 species fall into three groups, i.e. Sect. Sarcorhizoma, Sect. Lomatogonium and Sect. Pleurogynella. The former comes at a lower level with more plesiomorphies while the latter at a higher level with
more apomorphies. Lomatogonium is distributed in the northern temperate zone. However, 16 species are centred in Asia and two extend to Europe, or further to the Arctic region, but none has been found from Africa, Australia and South  erica. The analysis of distribution pattern of species shows that the Qinling-Hengduan Mountain region is both the frequence and diversity centers of Lomatogonium. From the cladogram of Lomatogonium (Fig. 5 ), L. perenne appears to occupy the most plesiomorphic node. This is an indication that it is the extant species closest to the ancestral form and it also implies that the ancestral species may reside in the habitat of this species (the Qinlin-Hengduan Mountain region). On the other hand, a  umber of species of Swertia Sect. Swertia also occur in this region today, which indicates that the Qinlin-Hengduan Mountain region may well be the original center of Lomatogonium. From the distribution pattern of L. rotatum, it can be concluded that the time of the origin dates back at least before the Pliocene. After emergence, this genus had first developed and dispersed in the original center and adjacent region, then diverged into two lineages. One gave rise to the widespread species (northern temperate distribution species L.
carinthiacum and L. rotatum), and the other formed the Himalayan species.
A taxonomic revision of the whole genus Lomatogonium is presented.  In this paper, one new section (Sect. Sarcorhizoma), one new species (L. zhongdianense S. W. Liu et T. N. Ho) and one new variety (L. forrestii var. densiflorum S. W. Liu et  T. N. Ho) are described. The key to the species is given. Type studies are made for all the taxa.
Comparative Studies on Photosynthetic Fluorescence Spectra and Fluorescence Kinetics of Bryophytes
Shi Ding-Ji, Wu Pan-Cheng, Qiu Yuan-Yuan, Wang Mei-Zhi
1992, 30 (4): 320-330. 
Abstract ( 0 )
Bryophytes  are  the  transitional  forms  from  water  habitants  to
terrestrials, however, there have been only a few works on their photosynthesis.
It was the first time to study on photosynthetic fluorescence spectra  and
fluorescence kinetics of primitive and advanced species comparatively. Both the
primitive and  advanced  ones  had  the  same  fluorescence  spectra  at  room
temperature,  which contained two maximum emissions:  F686-690 from the
Photosystem II and F736-740 from the Photosystem I. And then, there were three
maximum emissions in the fluorescence spectra at 77K :F687-689 and F697-699 from
Photosystem II, and F723-734 from Photosystem I. The first two maximum
emissions were the same for both the primitive and advanced species. According
to the third maximum emission the bryophytes under study fell into two
categories: The first one possessing the maximum emission around 725 nm,
including   Ditrichum   flexicaule ,   Didymodon   icmadophyllum ,   Didymodon
rigidicaulis,  Aloina  obliquifolia,  Plagiomnium  confertidens  and Marchantia
polymorpha,  which were primitive mosses and advanced liverwort. The second
one possessing the maximum emission around  732nm,  including  Thuidium
delicatulum ,   Pylaisia   brotheri ,   Myuroclada   maximowiczii ,   Taxiphyllum
taxirameum, Gollania neckerella, Eurohypnum leptothallum, which were advanced
mosses,  and the primitive one Plagiomnium rostratum.  The characteristics of
fluorescence spectra implied that the Photosystem  II was conservative  and
Photosystem I was changeable during bryophyte evolution. The primitive mosses
possess mainly the PSI core complex (CPI) and then the advanced species contain
both CPI and LHC-I.  In analysis of photosynthetic fluorescence kinetics,
 Fv/(Fc+Fv)  is a measure of the activity of the Photosystem II; Fv/Fm is dependent
 on efficiency of primary photoconversion in the Photosystem II; Fm/(Fo+Fv) is
related to photosynthetic carbon assimilation; and Fd/Fs is a measure of the
potential photosynthetic quantum conversion. The fluorescence kinetics of the
bryophyte photosynthesis showed that the Photosystem II activity, the efficieiency of
primary photoconversion in Photosystem II, the photosynthetic carbon assimila-
tion and the efficiency of the potential photosynthetic quantum conversion in
primitive species, such as Ditrichum flexicaule, Didymodon icmadophyllus, D.
rigidicaulis, Plagiomnium rostratum  and the liverwort Marchantia polymorpha,
were lower than  those in the advanced species,  Myuroclada maximowiczii,
Pylaisia  brotheri ,  Gollania  neckerella  Taxiphyllum  taxirameum ,   Thuidium
delicatulum. However, the primitive Plagiomnium confertidens was of the high
activities and efficiencies and the advanced Eurohypnum leptothallum was of low
ones. It seemed that P. confertidens and E. leptothallum were an intermediate
from the primitive to the advanced.
The Karyotype Analysis of Arthrotaxis (Taxodiaceae) and Its Systematic Position
Li Lin-Chu
1992, 30 (4): 331-341. 
Abstract ( 0 )
The present paper deals for the first time with an analysis of the
karyotypes of Athrotaxis cupressoides Don and A. selaginoides Don endemic to
Tasmania (Australia). Their morphology of somatic chromosomes in seed root-tip
cells, chromosome measurements, and diagrams are shown in Plate 1, Table 1
and  Fig. 1  respectively,  The karyotypic formulas of the  two  species  are
2n = 22 = 22m (2SAT) and 2n = 22 = 20m(2SAT ) + 2sm according to of terminolo-
gy Lexvan et al (1964). They all belong to IB type of Stebbins’(1971)karyotypic
asymmetry which was reported for the first time in the higher plants by
Li(1987b). Their chromosome complements are 22 = 2L + 10M2+ 8M1+ 2S and 22
=2L+ 10M2+ 6M1+ 4S respectively according to the standard defined by Kuo et
al. (1972) based on relative length. The karyotype of A. selaginoides is more ad-
vanced than that of A. cupressoides.
    In the light of karyotypic data, the sequence of the taxo-diaceous genera (excl.
Sciadopitys)  from  primitive  to  advanced  may  be  in  the  following  order:
Cryptomeria,  Glyptostrobus,  Taxodium,  Metasequoia,  Sequoiadendron,  Sequoia,
Athrotaxis, Cunninghamia and Taiwania. The genus Athrotaxis is closely related
to Sequoia (Sequoiadendron) and Cunninghamia The peculiarity of the karyotype
of Athrotaxis deserves the establishment of a new status Arthrotaxoideae (Wettste-
in) L. C. Li This suggestion is also supported by the data from morphology,
embryology, palynology and geography. The family Taxodiaceae is divided into
six subfamilies and nine genera, as shown in the following table:
—————————————————————————————————————————————————
    1. Cryptomerioideae Hida Cryptomeria D. Don               4. Arthrotaxoideae (Wettstein) L. C. Li
    2. Taxodioideae Pilger Glyptostrobus Endl. Taxodim  Richard    Athrotaxis D. Don
    3. Sequoideae Saxton metasequoia Miki ex Hu et             5. Cunninghamioideae Hida Cunninghamia
        Cheng Sequoiadebron Buch. Sequoia Endl.                   R.Brown
                                                              6. Taiwanioideae (Hayata)L. C. Li
                                                                                Taiwanta Hayata
—————————————————————————————————————————————————
The systematic positions of Athrotaxis in the systems of other authors are dis-
cussed too.
Karyotypes of Eleven Species of Triticeae in Northeast China
Sun Yi-Kai, Zhao Yu-Tang, Dong Yu-Chen, Zhou Rong-Hua, Xu Shu-Jun
1992, 30 (4): 342-345. 
Abstract ( 0 )
In  this  paper the karyotypes of eleven  species  of  Triticeae  from
Northeast China are reported. The karyotype formulae are as follows: Agropyron
cristatum,  2n=4x=28=20m+8sm;  Elytrigia repens,  2n=6x=42=34m(2SAT)
+ 8sm;  Hordeum  brevisubulatum,  2n = 4x = 28 = 20m + 8sm( 4SAT );  Roegneria
nakaii,  2n = 4x = 28 = 20m + 8sm( 4SAT );  R.  turczaninovii  var.   macrathera,
2n = 4x = 28 = 20m(2SAT ) + 8sm(2SAT ); Elymus sibiricus, 2n = 4x = 28 = 20m + 8sm
( 4SAT);  E.  dahuricus,  2n=6x=42=32m+10sm( 6SAT);  E.  excelsus,
2n=6x=42=32m+10sm( 6SAT); Leymus chinensis,  2n=4x=28=20m(4SAT)
+ 8sm; Roegneria ciliaris, 2n = 4x = 28 = 22m( 2SAT ) + 6sm( 2SAT ); R. kamoji,
2n= 6x = 42= 30m+ 12sm(4SAT). The karyotypes of the first five species are re-
ported for the first time.
The Chromosome Numbers of 10 Species in the Genus Campylotropis (Fabaceae)
Gao Xin-Fen, Gu Zhi-Jian, Chen Cheih
1992, 30 (4): 346-348. 
Abstract ( 0 )
This paper reports chromosome numbers of ten species and one variety
of the genus Campylotropis from China (Table 1, Plate 1 ). They are C. argentea
Schindl.,  C.  bonatiana( pamp: ) Schindl.,  C.  henryi  Schindl.,  C.  hirtella
(Franch.)Schindl., C. macrocarpa(Bunge )Rehd., C. diversifolia( Hemsl. )Schindl.,
C.  polyantha (Franch.) Schindl.,  C.  polyantha( Franch.  )Schindl.  var.
leiocarpa ( Pamp. ) Pet.  -Stib.,  c. prainii ( Coll.  et Hemal. ) Schindl.,  C.
pinetorum (kurz)Schindl. ssp. velutina (Dunn)Schindl., c. trigonoclada(Franch. )
Schindl. The chromosome numbers of these ten species are all 2n= 22 or n= 11,
but a few individuals in C. polyantha(Franch. )Schindl. var. leiocarpa(Pamp. )Pet.
-Stib., were found aneuploid with 2n=23. The chromosome numbers of c.
polyantha and C. macrocarpa have been reported by Maw-shing (1986)and
Lee(1972), while those of all the other species are first reported.
The Ecogeographical Distribution of Hippophae rhamnoides Subsp. sinensis and Its Phytogeographical Significance
Lian Yong-Shan, Chen Xue-Lin
1992, 30 (4): 349-355. 
Abstract ( 0 )
Hippophae rhamnoides L. subsp. sinensis Rousi is confined to China.
 The subspecies, a primitive member of the genus, is one of important plant
 resources for food and medicinal industry and also a genetic resource for breeding.
 The subspecies ranges from Southwest to Northeast China, i .e .from the northeast
part of Tibet to the sourthwest corner of the Da Hinggan Mountains ,through
Loess Plateau. Made in this paper was an analysis of the limits of tolerance, the
limiting factors and the fittest value, and of ecological factors regulating the
distribution area of the subspecies such as heat, sunshine and rainfall. The analy-
sis is based on comparison of the similarities between the distribution range and
the isolines of the various ecological factors, combined with the field work of the
subspecies.  The result  indicates  that  not  only  does  the  bush of Hippophae
rhamnoides L. subsp. sinensis Rousi occupy a stable geographical range, but also
it shows a zonal distribution pattern, controlled by rainfall and heat. Its geo-
graphical range is roughly located in the transitional zone of three vegetation re-
gions in China, i.e. the east moist forest region, the northwest desert and
steppe region and the Qinghai-Xizang Plateau alpine vegetation region. Therefore,
the bush can be used for delimitating the three vegetation regions. This fact
implies that the concept should be revised that the distribution of bushes is not of
obvious horizontal-zonal pattern. Also discussed in the present paper are ecological
conditions for the artificial Seabuckthron’s garden, the relationship between the
geographical range and the planting system in agriculture as well as the afforestation.
Genus Novum Gesneriacearum Vietnam
Wang Wen-Tsai, Li Zhen-Yu
1992, 30 (4): 356-361. 
Abstract ( 0 )
In 1926, based on a specimen (Poilane 3846) collected from Vietnam,
F. Pellegrin described a new species of the genus Hemiboea. Recently, after dis-
secting a flower of the holotype we realized that this species was erroneously
placed  in  Hemiboea,  differring  from  the  latter  in  a  series  of important
morphological characters, and in fact represents a new genus (Deinostigma) of
the tribe Didymocarpeae, which is described in the present paper.
New Taxa of the Genus Agrostis from Yunnan
Wang Yang-Cai, Sun Bi-Sin
1992, 30 (4): 362-366. 
Abstract ( 0 )
In the paper two species and one variety of the genus Agrostis L. are
described as new from Yunnan Province, China. They are Agrostis lushuiensis,
A. kunmingensis and A. myriantha Hook. f. var. yangbiensis.
New Taxa of Lappula from China
Wang Xiao-Dong, Wang Ching-Jui
1992, 30 (4): 367-370. 
Abstract ( 0 )
Two new species and one new variety are described from China.  They are L.
ramulosa, L. gansuensis and L. microcarpa var. heterogenea.
New Taxa of Lespedeza (Leguminosae) from China
Chen Chia-Jui
1992, 30 (4): 375-377. 
Abstract ( 0 )
Lespedeza fasciculiflora Franch. var. hengduanshanensis C. J. Chen
and L.  davurica (Laxm.)  Schindl.  Subsp. huangheensis C.  J.  Chen are
described from the Hengduan Mountains of SW China and from the Yellow River
valley respectively.
A New Species of Ranunculus L. from Xinjiang
Liu Jian-Guo
1992, 30 (4): 378-380. 
Abstract ( 0 )
 A new species of the genus Ranunculus L., R. hamiensis J . G. Liu, is
described from Xinjiang.
Materials for the Cyanophytes From China
Li Yao-Ying
1992, 30 (4): 381-384. 
Abstract ( 0 )
 In this paper, two new species and two new records of Gyanophytes from China are
reported. They are Hyella rupicola Y. Y. Li; Camntytonema quandongensis Y. Y. Li; Pseudoholo
pedia convoluta (Breb.) Elenk; Lithnema adriaticum Frceg.