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1991, Vol.29, No.6 Previous Issue    Next Issue
A Phylogenetic Analysis of Families in the Hamamelidae
Lu An-Ming, Li Jian-Qiang, Xu Ke-Xue
1991, 29 (6): 481-493. 
Abstract ( 0 )
 A cladistic analysis of the families in the Hamamelidae is made in the present pa-
per. As a monophyletic group, the subclass Hamamelidae includes 19 families, namely, the
Trochodendraceae,  Tetracentraceae,  Cercidiphyllaceae,  Eupteleaceae,  Eucommiaceae,
Hamamelidaceae (incl. Rhodoleiaceae and Altingiaceae), Platanaceae, Daphniphyllaceae,
Balanopaceae, Didymelaceae, Myrothamnaceae, Buxaceae, Simmondsiaceae, Casuarinaceae,
Fagaceae (incl. Nothofagaceae), Betulaceae, Myricaceae, Rhoipteleaceae and Juglandaceae.
The Magnoliaceae was selected for outgroup comparison after careful consideration.
Thirty-two informative character states were used in this study. Three principles, namely,
outgroup comparison, fossil evidence and generally accepted viewpoints of morphological
evolution, were used for polarization of the characters. An incompatible number concept was
first introduced to evaluate the reliable degree of polarization of the characters and, by this
method, the polarization of the three character states was corrected.
     A data matrix was constructed by the 19 ingroup families and 32 character states. The
data matrix was analysed with the Minimal Parallel Evolutionary Method, Maximal Same
Step Method (Xu 1989), and Synthetic Method. Three cladograms were constructed and a
parsimonious cladogram (Length= 131)was used as the base for discussing the systematic re-
lationships of families in the Hamamelidae.
     According to the cladogram, the earlist group differented in the subclass Hamamelidae
consists of two vesselless wood families, the Trochodendraceae and Tetracentraceae. This re-
sult supports the concept proposed by Takhtajan (1987)and Cronquist (1981, 1988)that the
Trochodendrales is probably a primitive taxon in the Hamamelidae.
     As in a clade group, the Cercidiphyllaceae, Eucommiaceae, Balanopaceae and
Didymelaceae originated apparently later than the Trochodendrales. The Cercidiphyllaceae
diverged earlier in this group, which implies that this family and the Trochodendrales form a
primitive group in the subclass. The Cercidiphyllaceae is either placed in Hamamelidales
(Cronquist 1981, Thorne 1983), or treated as an independent order (Takhtajan 1987).This
analysis suggests that the Cercidiphyllaceae is a relatively isolated taxon, far from the
Hamamelidaceae but close to the Trochodendrales in relation. The Eucommiaceae and
Didymelaceae are both isolated families and considered as two distinct orders (Takhtajan
1987, Cronquist 1981, 1988).The Balanopaceae is included in the Fagales (Cronquist 1981,
1988) or Pittosporales (Thorne 1983), or treated as a distinct order Balanopales (Takhtajan
1987 ).Obviously the Balanopaceae and Eucommiaceae are not closely related because of the
sole synapomorphy (placentation).In fact these four families are more or less isolated taxa
and it is probably more reasonable to treat them as independent orders.
     Cronquist ( 1981, 1988) places the Eupteleaceae, Platanaceae and Myrothamnaceae in
the Hamamelidales, while Takhtajan (1987)puts Hamamelidaceae and Platanaceae into the
Hamamelidales and treats the Eupteleaceae and Myrothamnaceae as two independent
monofamilial orders. These three families are grouped by more synapomorphies (palmate-
veined, serrate or lobate leaves, deciduous and anemophilous plants)which may indicate their
close phylogenetical affinity.
     A core group of the Hamamelidae includes ten families, among which the Hama-
melidaceae originated earlier than the others, so that it is a relatively primitive family.
     The Betulaceae, Fagaceae and Myricaceae differentiated later than the Hamamelidaceae.
The former two are very closely related, and thus thought to be two neighbouring orders by
Takhtajan (1987)or included in the Fagales by Cronquist (1981, 1988)and Thorne (1983).
The Myricaceae and Fagaceae are connected in the cladogram by only a single
synapomorphy (endosperm absent), and therefore the close relationship does not exist be-
tween them.
     The Buxaceae, Simmondsiaceae and Daphniphyllaceae form an advanced group, in
which they are weakly linked with each other by only one synapomorphy (pollen
grains<25μm). The Daphniphyllaceae is closely related to the Simmondsiaceae, but the
Buxaceae is rather isolated.
     The Rhoipteleaceae and Juglandaceae share a number of synapomorphies (axile
placentation, endosperm absent, embryo larger, fruit indehiscent) , forming a highly
specialized group. The opinion that the Juglandales is composed of the Juglandaceae and
Rhoipteleaceae(Cronquist 1981; 1988, Lu et Zhang 1990)is confirmed by this analysis. A
contrary point of view, which treated them as two distinct orders by Takhtajan (1987), appar-
ently could not be accepted.
     The Casuarinaceae was regarded as the primitive angiosperm (Engler 1893), but in fact
it is a highly reduced and specialized group. It is united with Rhoipteleaceae and Juglandaceae
by four synapomorphies, i. e. placentation type, endosperm absent, embryo large and fruit
indehiscent. However, the family presents six autapomorphies, and thus the position of the
Casuarinaceae as an advanced family is confirmed by this analysis.
     Finally a strict consensus tree, which represents the phylogenetic relationships of the
families in the Hamamelidae, was given as a result of the analysis.
Pollen Morphology of the Betulaceae
Chen Zhi-Duan
1991, 29 (6): 494-503. 
Abstract ( 0 )
Pollen grains of 6 genera, including 36 species, of the Betulaceae, were examined
under LM, SEM and TEM.Their morphological characters are described and three types of
pollen are distinguished here. The evidence from pollen morphological characters does not
support Hutchinson's (1973)and Dahlgren's (1983)treatments which divided the Betulaceae
into two families: Corylaceae ( including Corylus, Ostryopsis, Carpinus  and Ostrya) and
Betulaceae (including Alnus and Betula). The author agrees with Abbe's (1974)division of
the Betulaceae into three tribes with one modification that Ostryopsis is transferred from the
tribe Coryleae to the tribe Carpineae. The limits of the three tribes presented here are the same
as Kuprianova's (1963) treatment in which she divided the Betulaceae into three families. It is
more reasonable to treat Kuprianova's families as tribes. Pollen morphological characters of
the three tribes of the Betulaceae are described as follows:
      1. Tribe Betuleae (including  Alnus  and  Betula):  Pollen grains are triporate or
stephanoporate and oblate, suboblate or spheroidal. Sometimes the exine has arci and the
ektexine thickens in the apertural region; the sculpture of exine is slightly rugulate under
scanning electron microscope (SEM) ; the exine structure is four-layered: tectum,
columellae, footlayer and endexine. The columellae are columellate, the endexine thickens in
the apertural region and sometimes it is separated from the footlayer to form vestibulum.
     2. Tribe Coryleae (only Corylus): Pollen grains are triporate and suboblate. The exine
has no arci and the ektexine does not thicken in the apertural region; the sculpture of exine is
slightly rugulate under SEM; the exine structure is five-layered: granular layer, tectum,
columellae, footlayer and endexine. The tectum is vovered with a granular layer, the
columellae granular and the endexine thickens but is not separated from the footlayer in the
apertural region.
     3. Tribe Carpineae (including  Ostryopsis, Carpinus and  Ostrya): Pollen grains are
mostly triporate and suboblate. The exine has no arci and the ektexine does not thicken in the
apertural region; the sculpture of exine is slightly rugulate under SEM; the exine structure is
five-layered which is the same as those of the Coryleae. The tectum is covered with a
granular layer, the columellae are columellate and the endexine is neither thickened nor sepa-
rated from the footlayer in the apertural region. The operculum exists on the top of aperture
membrane.
The Embryology of Nyssa sinensis Oliv. (Nyssaceae)
Chen Ling-Jing, Qian Nan-Fen, Wang Fu-Hsiung
1991, 29 (6): 504-510. 
Abstract ( 0 )
The flower develops in March and blossoms in early May in Nanjing. The
cytokinesis of microsporocytes is simultaneous and most tetrads are tetrahedral. The tapetum
is secretory and the nuclei become polyploid at last. The style is solid and most ovaries are
unilocular, rarely bilocular. The ovule is pendulous, anatropous and unitegmic. The nucellus is
pseudocrassinucellate. An obturator formed by transmitting tissue covers the micropyle. The
raphe vascular strand extends into the integument when it reaches the chalaza and on a whole
keeps a “U” shape. The endothelium cell is uninucleate. In most cases no nucellar cap is
formed. No hypostase is found below the embryo sac. The archesporium is one-celled. The
embryo sac development conforms to the Polygonum or Allium types. The degeneration of
the megaspores in the linear tetrad usually occurs from the chalazal toward the micropylar
end. Two synergids persist during fertilization. Three antipodal cells are uninucleate and
ephemeral. Two polar nuclei fuse at the time of fertilization. The fertilization type accords
with porogamy. The syngamy is premitotic. The development of endosperm is cellular.
The initial four successive divisions of the primary endosperm cell are transverse-vertical-
transverse-transverse subsequently, giving rise to sixteen cells of the early endosperm. The
mature embryo is straight and nearly as long as the endospermous seed. The cotyledons are
more or less cordate at base. The seedoat is thin and composed of 5-11 layers of compressed
cells. Neither embryo nor endosperm contain the alkaloid camptothecine.
     The major similarities of Nyssa sinensis to the American nyssas in embryology, which
may be a counted as the generic features, are the polyploid tapetum cells, the unitegmic ovule
with U-shaped vascular strand, the direct enlargement of the archesporial cell to produce the
megasporocyte, the pseudocrassinucellus, the usual absence of the nucellar cap, the
Polygonum or Allium type of the embryo sac development, the first degeneration of the
metachalazal megaspore, the ephemeral antipodal cells, a single nucleolus in the nucleus of
the primary endosperm cell, the more or less cordate base of the cotyledons.
Variation and Phylogenetic Relationships Between Polygonatum odoratum and P. cyrtonema
Wang Jin-Wu, Li Mao-Xue, Yang Ji
1991, 29 (6): 511-516. 
Abstract ( 0 )
The present paper is a report on combined cytological and taxonomical studies
of Polygonatum odoratum and P. cyrtonema. Based on the extensive field observation and
mass collection for some years, the authors made a detailed comparison of the variation pat-
tern of morphology、cytology as well as geographic distribution between forms
of P. odoratum and P. cyrtonema. The results show that: Form I: Stem angular, leaves
elliptic, peduncles with one, rarely two flowers, perianth 1.7-2.0 cm long, stamens adnate to
perianth in the middle part or a little lower. The karyotype formula is 2n=20=12m+8sm
(2SAT); Form II: Stem angular, leaves narrow-oblong, peduncles with 2-3 flowers,
perianth 2.8-3.2 cm long, the position of stamens on perianth is above the middle part.
It has the karyotype 2n=20=8m+1osm(4SAT)+2st; Form III: Stem terete, leaves
oblong-lanceolate, peduncles with 3- 10 flowers, perianth 1.5- 2.0cmlong, stamens are
adnate to perianth also above the middle part. In this form, two kinds of karyotypes are
found: 2n = 22 = 6m+8sm+8st and 2n = 20 = 4m+6sm (2SAT) +10st; Form IV: Stem terete,
leaves elliptic, peduncles with 1-4 flowers, perianth 2.3-2.8 cmlong, stamens adnate to
perianth above the middle part. The karyotype formulae are 2n = 20 = 4m+14sm (2SAT)+2st
and 2n = 20 = 10m+10sm (2SAT); Form V: Stem terete, leaves oblong-lanceolate, peduncles
with 3-5 flowers, perianth less than 2.0cm long, stamens adnate to perianth above the mid-
dle part. It is of the karyotype 2n=22=4m+8sm(2SAT) +10st. It is pointed out that
the P. odoratum collected from the Qinling Range may be a hybrid or an intermediate in the
evolutionary process from P. odoratum to P. cyrtonema. The differences between the differ-
ent forms of P. cyrtonema are obvious and stable, and are probably derived from the
chromosomal  variation. The  different  forms  of P. cyrtonema  may  have  evolved
from P. odoratum along different courses.
A Study on the Genus Acidosasa of Bambusoideae
Chao Chi-Son, Chu Cheng-De
1991, 29 (6): 517-524. 
Abstract ( 0 )
The genus Acidosasa was published by the present authors in 1979. It only had one
species at that time, Acidosasa chinensis C. D. Chu et C. S. Chao. Since then species number
of the genus steadily increases. The authors have rather comprehensively studied this genus
and its related genera for F1. Reip. Pop. Sin. The present paper deals mainly with
morphological characteristics of the genus Acidosasa and the differences from its related gen-
era i. e. Arundinaria, Sasa and Indosasa. The genus Acidosasa is closely related to the genus
Arundinaria in the type and origin of inflorescences and the vegetative appearance. But it dif-
fers from Arundinaria in the structure of florets. In Acidosasa, each floret is provided with six
stamens, while in Arundinaria each floret is of only three stamens. The genus Acidosasa is sim-
ilar to the genera Indosasa and Sasa in the numbers of stamens, but it is distinguished from
lndosasa by its semelauctant (determinate) inflorescence, not iterautant (indeterminate) one,
from Sasa by its taller stature and branch complement with three branches.
     We have carefully examined all the type specimens of Acidosasa and its related genera. A
conclusion reached is that there are six species in the genus Acidosasa, most of which are na-
tive to S. China, with only one species in Viet Nam. Five specific binomials are reduced and
one species is transferred into this genus. Two keys to species, respectively based on the flow-
ering and vegetative characters, are given as follow:
             Key to species of the genus A cidosasa (1)(based on the flowering state)
1. Lemmas glabrous.
  2. Spikelets stout, 3-6mm broad, pedicels 1.5-4cm long; lemmas large, 1.5-2.2cm long,
      with 15-19 nerves, subcoriaceous, not glaucous, shiny.
     3. Lemmas up to 2.2cm long with conspicuously transverse veinlets, tessellate; palea and
         rhachilla entirely. glabrous, lodicules elliptic-lanceolate, glabrous  ... 1. A. chinensis
     3. Lemmas 1.5-1.8cm. long, slightly tessellate; palea puberulous at apex of carina,
         rhachilla puberuous at apex, lodicules obovate, ciliate at apex  ............  2. A. brilletii
  2. Spikelets rather slende, 2-4mm broad, pedicels 0.5-1cm long; lemmas small, about
      1.3 cm long, with 7-13 nerves, more or less glaucous  .......... 3. A. chienouensis
1. Lemmas pubescent.
  4. Glumas and lemmas densely pubescent  ........................  4. A. hirtiflora
  4. Glumas subglabrous, lemmas sparsely pubescent.
    5. Spikelets large, 3-7 cm long, lemmas 1.6-1.7 cm long, pedicels 2-13 mm long
           .................................................  5. A. longiligula
    5. Spikelets small, 2-3.7 cm long, lemmas about 1.3 cm long, pedicels 1-3 cm long
            ...................................................  6. A. venusta
         Key to species of the genus A cidosasa (2) (based on the vegetative state)
1. Ligules of leaf-sheaths strongly elevated, usually 2-8 mm long.
  2. Young culms with bristly sheath scars; culm-sheaths without auricles and oral
     setae, not spotted, sheath-blades erect  .................  4. A. hirtiflora
  2. Young culms with glabrous sheath scars; culm-sheaths with small auricles and oral
     setae, sparsely spotted, sheath-blades reflexed  ..........  5. A. longiligula
1. Ligules of leaf-sheaths inconspicuous, less than 2 mm long.
  3. Young culms more or less bristly, or sheath-scars bristly:
    4. Culm-sheaths without auricles and oral setae, not farinose, without hairs at base.
       5. Young culms densely bristly; culm-sheaths attenuate at apex and as wide as
          sheath-blades, with conspicuously transverse veinlets; leaf-blades large, usual-
          ly 2.5-3.5 (-6.5) cm broad, conspicuously tessellate
             .....................................................  1. A. chinensis
       5. Young culms sparsely bristly; culm-sheaths truncate at apex and broader than
          sheath-blades, without transverse veinlets or inconspicuous; leaf-blades small,
          1.5-2.5 cm broad, without visible transverse veinlets
              ....................................................  6. A. venusta
    4. Culm-sheaths with auricles and oral setae, slightly farinose, densely bristle at
       base; leaf-blades rather narrow, 0.8-1.8 cm broad  ............  3. A. chienouensis
  3. Young culms entirely glabrous; leaf-blades rather narrow, 1.2-1.8 cm broad
         .......................................................................................  2. A. brilletill
Two New Species of Cymbidium from China
Wu Ying-Siang, Chen Sing-Chi
1991, 29 (6): 549-552. 
Abstract ( 0 )
A New Species of Sonchus from China
Shih Chu
1991, 29 (6): 553-554. 
Abstract ( 0 )