MICRO-MACROMORPHOLOGLYCAL STUDY OF THE GENUS
CICER L. (FABACEAE) IN IRAN
F. Sharifnia, T. Farhani & F. Salimpour
Sharifnia, F., Farhani, T. & Salimpour, F., 2006 12 31: Micro-macromorphological study of the genus
Cicer L. (Fabaceae) in Iran. -Iran. J. Bot. 12 (2): 147-162. Tehran.
In this study, eleven species of genus Cicer L. were studied and morphological and micromorphological characters were evaluated. These species are classified in 4 sections: Monocicer,
Chamaecicer, Polycicer and Acanthocicer. The understudied species assessed by biometric study, and
about 40 quantitative and 38 qualitative characters were assessed. Phenetic analysis was carried out
using SPSS software, and phenograms of these species were prepared. Furthermore, PCA analysis
was carried out and the most variable characters were determined. Finally, the seeds and pollen of
these species were also investigated using S. E. M electronic microscope, and the tables of characters
were formed individually for them. Afterward, phenetic analysis and phenogram preparation were
done based on morphological characters of seeds and pollen of the species, and the following results
were obtained:
1.Distinction of C. kermanense Bornm., as an independent species, from C. spiroceras Juab. & Spach,
in contrary to what mentioned in Flora of Iran. 2. Transferring C. subaphyllum Boiss. from Polycicer
section to the Acanthocicer section. 3. In spite of leaf polymorphism seen in C. tragacanthoides Jaub.
& Spach, it seems that the pollen characters are sufficient to devide it to varieties. 4. Division of
species of this genus using quantitative and qualitative specifications of seeds. 5. Preparation of the
table of characters for pollen and seeds of all species .
Fariba Sharifnia, Tayebbeh Farhani & Fahimeh Salimpour, Department of Biology, Faculty of
Science, Islamic Azad University, North Tehran Branch, P. O. BOX 19585-936 Tehran, Iran.
Key words. Micro-macromorphology, phenetic analysis, Iran, Cicer.
( ﺩﺭ ﺍﻳﺮﺍﻥCicer L.) ﻣﺎﻛﺮﻭﻣﻮﺭﻓﻮﻟﻮﮊﻱ ﮔﻮﻧﻪﻫﺎﻱ ﺟﻨﺲ ﻧﺨﻮﺩ-ﻣﻄﺎﻟﻌﻪ ﻣﻴﻜﺮﻭ
ﻃﻴﺒﻪ ﻓﺮﻫﺎﻧﻲ ﻭ ﻓﻬﻴﻤﻪ ﺳﻠﻴﻢ)ﻮﺭ،ﻓﺮﻳﺒﺎ ﺷﺮﻳﻒ ﻧﻴﺎ
ﻛﻠﻴﻪ اﻳﻦ. ﻣﻮرد ﻣﻄﺎﻟﻌﻪ و ﺑﺮرﺳﻲ ﻣﻮرﻓﻮﻟﻮژﻳﻜﻲ و ﻣﻴﻜﺮوﻣﻮرﻓﻮﻟﻮژي ﻗﺮار ﮔﺮﻓﺖCicer L. ﮔﻮﻧﻪ از ﺟﻨﺲ11 در اﻳﻦ ﻣﻄﺎﻟﻌﻪ
ﮔﻮﻧﻪﻫﺎ ﻣﻮرد ﻣﻄﺎﻟﻌﻪ. ﻗﺮار دارﻧﺪAcanthocicer وPolycicer, Chamaecicer, Monocicer ﮔﻮﻧﻪﻫﺎ در ﭼﻬﺎر ﺑﺨﺸﻪ
آﻧﺎﻟﻴﺰ ﻓﻨﺘﻴﻜﻲ ﺑﺎ اﺳﺘﻔﺎده.ﺑﻴﻮﻣﺘﺮي ﻗﺮار ﮔﺮﻓﺖ و ﺗﻌﺪاد ﭼﻬﻞ ﺻﻔﺖ ﻛﻤﻲ و ﺳﻲ و ﻫﺸﺖ ﺻﻔﺖ ﻛﻴﻔﻲ ﻣﻮرد ﺳﻨﺠﺶ ﻗﺮار ﮔﺮﻓﺖ
اﻧﺠﺎم ﮔﺮﻓﺖ و ﻣﺘﻐﻴﺮﺗﺮﻳﻦ ﺻﻔﺎت ﻣﺸﺨﺺPCA ﻫﻤﭽﻨﻴﻦ آﻧﺎﻟﻴﺰ. اﻧﺠﺎم ﺷﺪ و ﻓﻨﻮﮔﺮام ﮔﻮﻧﻪﻫﺎ ﺗﻬﻴﻪ ﮔﺮدﻳﺪSPSS از ﻧﺮماﻓﺰار
ﻗﺮار ﮔﺮﻓﺖ و ﺟﺪولS. E. M. در ﻧﻬﺎﻳﺖ داﻧﻪ و ﮔﺮدهﻫﺎي اﻳﻦ ﮔﻮﻧﻪﻫﺎ ﻫﻢ ﻣﻮرد ﺑﺮرﺳﻲ ﺑﺎ ﻣﻴﻜﺮوﺳﻜﻮپ اﻟﻜﺘﺮوﻧﻲ.ﺷﺪﻧﺪ
ﺳﭙﺲ آﻧﺎﻟﻴﺰ ﻓﻨﺘﻴﻜﻲ و ﺗﻬﻴﻪ ﻓﻨﻮﮔﺮام ﺑﺮاﺳﺎس ﺻﻔﺎت ﻣﻮرﻓﻮﻟﻮژي ﺑﺬر و ﮔﺮده ﮔﻮﻧﻪﻫﺎ،ﺻﻔﺎت ﺟﺪاﮔﺎﻧﻪاي ﺑﺮاي آﻧﻬﺎ ﺗﺸﻜﻴﻞ ﺷﺪ
:اﻧﺠﺎم ﺷﺪ و ﻧﺘﺎﻳﺞ زﻳﺮ ﺑﻪ دﺳﺖ آﻣﺪ
C. spiroceras Jaub. & ﺑﻪ ﻋﻨﻮان ﻳﻚ ﮔﻮﻧﻪ ﻣﺴﺘﻘﻞ و ﺟﺪا از ﮔﻮﻧﻪC. kermanense Bornm. ﺟﺪا ﺷﺪن آراﻳﻪ-1
. ﺑﺮﺧﻼف آﻧﭽﻪ ﻛﻪ در ﻓﻠﻮر اﻳﺮان آﻣﺪه اﺳﺖSpach
. Acanthocicer و اﻧﺘﻘﺎل آن ﺑﻪ ﺑﺨﺸﺔPolycicer از ﺑﺨﺸﺔC. subaphyllum ﺟﺪاﻳﻲ ﮔﻮﻧﻪ-2
ﺑﻪ ﻧﻈﺮ ﻣﻲ رﺳﺪ ﺻﻔﺎت ﮔﺮده ﻗﺎدر ﺑﻪC. tragacanthoides Jaub. & Spach ﺑﺎ وﺟﻮد ﭘﻠﻲ ﻣﻮرﻓﻴﺴﻢ ﺑﺮﮔﻲ در ﮔﻮﻧﻪ-3
. ﻣﻲﺑﺎﺷﺪC. tragacanthoides ﺗﻔﻜﻴﻚ وارﻳﺘﻪﻫﺎي ﮔﻮﻧﻪ
. ﺗﻔﻜﻴﻚ ﮔﻮﻧﻪﻫﺎي اﻳﻦ ﺟﻨﺲ ﺑﺎ اﺳﺘﻔﺎده از ﺧﺼﻮﺻﻴﺎت ﻛﻤﻲ و ﻛﻴﻔﻲ داﻧﻪﻫﺎ-4
. ﺗﻬﻴﻪ ﺟﺪول ﺧﺼﻮﺻﻴﺎت ﮔﺮده و داﻧﻪ ﻛﻠﻴﻪ ﮔﻮﻧﻪﻫﺎ-5
IRAN. JOURN. BOT. 12 (2), 2006
Introduction
Genus Cicer L. belongs to the family Fabaceae and the
tribe Cicereae Alef., and it consists of 43 species, ten
anuuals and 33 perennials. About 39 species grow in
Middle Asia and West Asia, and about 4 species in
certain regions of north and northwestern areas of
Africa and Europe (van der Maesen 1987).
The basic chromosomal number for them is x = 8.
This genus consists of some herbaceous and shrubby
species which are classified into 4 sections on the basis
of morphological specifications and life cycle
characteristics (van der Maesen, 1987 and 1972).
1. The section Monocicer consists of the agronomic
species C. arietinum and 7 annual species including C.
reticulatum, C. bijugum, C. echinospermum, C.
judaicum, C. pinnatifidum, C. cuneatum, C.
yamashitae.
2. The section Chamaecicer consists of one annual
species and one perennial species which grow in
mountain areas in West Asia and Kert Island.
3. The section Polycicer consists of 25 perennial
species.
4. The section Acanthocicer consists of 7 perennial
species growing in mountain regions of Iran,
Afghanistan and Middle Asia (van der Maesen, 1987;
Popov, 1976).
In this paper, micro-macromorphological data was
subjected to cluster analysis in order to indicate the
Sharifnia & al. 148
species inter-relationship, to evaluate the previous
taxonomic treatment of the genus Cicer in Iran, and
provide the evidence for efficacy of micromacromorphological data in taxonomic treatment of
genus Cicer at sub-generic level.
Materials and Methods
In order to study morphological charactrs of plant
specimens in each species (at least 3 specimens), we
chose about 40 quantitative and 38 qualitative
characters.
The table of morphological characters was prepared
based on these qualitative and quantitative characters
(Table 1).
For statistical analysis, we initially encoded the
qualitative characters according to the multi-state
method, and the related means were considered for
quantitative characters, and then these were
standardized. Phenetic analysis was carried out using
SPSS, ver. 9 software and Ward method (Norusis1999).
Based on this method, we delivered a cluster analysis
for morphological characters of species and then
hierarchical phenograms of species were prepared.
PCA analysis was performed as well and the most
variable characters were specified.
Table 1. List of characters and related numerical codes used in morphological studies.
No.
Characters
Numerical code
1
Plant height
Cm
2
Stem diameter
Mm
3
Rachis length
Mm
4
Number of leaflets
In no.
5
Leaflet length
Mm
6
Leaflet width
Mm
7
Leaflet length / width ratio
In no.
8
Length of leaflet teeth
Mm
9
Number of leaflet teeth
In no.
10
Number of stipule teeth
In no.
11
Stipule length
Mm
12
Stipule width
Mm
13
Stipule length / width ratio
In no.
14
Calyx length
Mm
15
Length of calyx tube
Mm
16
Length of calyx teeth
Mm
17
Number of calyx teeth
In no.
18
Peduncle length
Mm
19
Pedicel length
Mm
20
Corolla length
Mm
21
Standard length
Mm
22
Standard width
Mm
23
Standard length / width ratio
In no.
24
Wing length
Mm
25
Wing width
Mm
IRAN. JOURN. BOT. 12 (2), 2006
149 Cicer morphology
No.
26
27
28
29
30
31
32
33
34
35
36
37
39
40
41
Characters
Wing length / width ratio
Keel length
Keel width
Keel length / width ratio
Pod length
Pod width
Pod length / width
Arista length
Seed length
Seed width
Seed length/width ratio
Pedicel / peduncle length ratio
Pedicel & peduncle/rachis length
ratio
Calyx teeth / tube length ratio
Corolla / calyx length ratio
Growth period
42
Growth habit
43
44
Stem shape
Epigaeal stem
45
Stem hairs
46
47
48
State of stem hairs
Size of stem hairs
Leaflets arrangment
49
End of rachis
50
Leaflet shape
51
Leaflet base
52
Leaflet apex
53
Leaflet margin
54
Leaflet hairs
55
Shape of upper stipules
56
Shape of lower stipules
57
Calyx gibbousity
58
Shape of calyx teeth
59
Position of calyx teeth
60
Calyx hairs
61
62
State of calyx hairs
Number of flowers per peduncle
63
Pedicel hairs
64
State of pedicel hairs
65
Corolla color
66
Standard shape
38
Numerical code
In no.
Mm
Mm
In no.
Mm
Mm
In no.
Mm
Mm
Mm
In no.
In no.
In no.
In no.
In no.
1- annual 2- perennial
1- erect-semi erect 2- prostrate to erect 3- prostrate 4- shrubby 5shrubby – cushion
1- straight to slightly flexuous 2- straight – flexuous 3- flexuous
1- absence 2- presence
1- glandular and simple 2- mostly glandular, rarely simple 3mostly simple, rarely glandular 4- simple 5- glandular
1- less 2-mean 3-more
1-long 2-long and short 3-short
1-imparipinnate 2- paripinnate and imparipinnate 3- paripinnate
1- unileaflet 2- in upper leaves, curled or simple and ramified
tendril. in lower leaves, leaflet 3-curled or simple and ramified
tendril 4- curled or simple tendril 5-spinelet or curl 6-spinelet
1-elliptic-obovate 2-obovate-oblong 3-cuneate-flabellate 4obovate 5-cuneate-ebovate 6-rounded- flabellate 7-spiny 8-upper
leaflet, spiny lower leaflet, fan shaped 9-ovate-flabellate
1-cuneate 2-rounded-cuneate 3-broadly cuneate
1-rounded or acuminate 2- rounded or truncate 3-rounded 4truncate 5-acute 6-upper leaflets acute and lower leaflets, rounded
1-serrate 2-entire 3- dentate at the apex
1- glandular and simple 2- mostly glandular, rarely simple 3mostly simple, rarely glandular 4- simple 5- glandular
1-hastate 2- entire 3- lanceolate
1- ovate or semiovate 2- ovate 3- oblique – triangular incised 4semiovate 5- triangular 6- lanceolate - triangular
1- faintly gibbous 2- middle gibbous 3- strongly gibbous
1- lanceolate 2- lanceolate–triangular 3- broadly lanceolate 4lanceolate – acuminate
1- almost equal 2- unequal
1- glandular and simple 2- mostly glandular, rarely simple 3- mostly
simple, rarely glandular 4- simple 5- glandular
1- less 2-mean 3-more
1- 1
2- 1-2
3- 1-4
1- glandular and simple 2- mostly glandular, rarely simple 3mostly simple, rarely glandular 4- simple 5- glandular
1- less 2-mean 3-more
1- blue, pink, white 2- purplish pink 3- cream + violet 4- purplish
5- purplish blue 6- lilac – white 7- lavender 8- pink – white 9white
1- obovate 2- ovate 3- elliptic – ovate
IRAN. JOURN. BOT. 12 (2), 2006
No.
67
68
69
70
71
72
Characters
Standard base
Standard apex
Wings shape
Wings base
Keel shape
Position of keel adnate
73
Pod shape
74
Pod hairs
75
76
State of pod hairs
Seed shape
77
Seed color
78
Seed coat texture
Sharifnia & al. 150
Numerical code
1- broad 2- spatula-shaped 3- non
1- less emarginated 2- mean emarginated
1- obovate 2- obovate – oblong 3- triangular 4- oblong
1- auriculate 2- short auriculate 3- long auriculate
1- rhomboid 2- oblong
1- 2/3 of ventral margin 2- 3/4 of ventral margin
1- elliptic - rhomboid 2- elliptic oblong 3- ovoid 4- elliptic obovate
5- elliptic
1- glandular and simple 2- mostly glandular, rarely simple 3- mostly
simple, rarely glandular 4- simple 5- glandular
1- less 2-mean 3-more
1- circular 2- subcircular 3- obovate 4- cordate
1- cream 2- brownish with black spot 3- grey brown with black
point 4- light brown 5- black brown 6- brown 7- reddish brown
1- wrinkled reticulate 2- spiny hairs + conical projection 3- shallow
protuberance 4-tuberculated 5- wrinkled tuberculated + acuminate
projection 6- tuberculated + irregularly curved 7- rugose –
reticulate + wrinkled tubercle 8- wrinkled tuberculated 9- flat
tuberculated 10- tuberculated reticulate 11- rugose
For morphological study of pollen and seed, we
used herbarium specimens and fresh materials in the
field (Table 2 & 3). Pollen grains and seeds were
stabilized on aluminum stocks and coated with a thin
layer of gold using coating equipment. Then, the
specimens were observed under S. E. M. electronic
microscope, model LEO 440 at the Islamic Azad
University, Research and Sciences Branch. For each
species, about 3 specimens of pollen and seeds were
studied, and finally the related images and tables of
morphological characters of pollen and seeds were
prepared.
Moore1991, was utilized for the terminology of the
pollen as reference and Zohary & Heller, 1984 and
Javadi & Yamaguchi, 2004 were utilized for
terminology of the seeds as references.
Result and Discussion
According to the phenogram, (fig. 1) in the linkage
distance 11, two original clusters are distinguishable. In
the first cluster, the C. incisum and C. chorassanicum
pertaining to the section Chamaecicer are located close
to each other (subcluster 1). Furthermore, two species
of C. arietinum and C. bijugum which belong to the
section Monocicer are also located adjacent to each
other (subcluster 2).
In turn, the 2nd cluster is divided into two
subclusters 1 and 2. The subcluster 1 consists of C.
anatolicum, C. oxyodon, C. kermanense, and C.
spiroceras which are located adjacent to each other.
These four species are located into Polycicer section,
and in the subcluster 2, C. tragacanthoides (var.
tragacanthoides and var. turcomanicum) and C.
stapfianum which belong to the section Acanthocicer,
are located. However C. subaphyllum from Polycicer
section appears in this group. In fact, this species due to
having some specifications such as spinous leaflets,
presence of spine or curl at the end of rachis and its
suffruticose appearance becomes distinguishable from
the other species in the section Polycicer, and instead it
should be placed in Acanthocicer section.
The differences between these two original clusters
mainly underlies even or odd arrangement of leaves,
status of the end of rachis and the calyx gibbousity
positioning.
The PCA analysis revealed that the most variable
characters are calyx gibbousity positioning,
specifications of ending of rachis, type of penducle
hairs, growth habit, length of vexillum, length of
carina, type of pod and calyx hairs, shape of lower
stipules, type of division of leaf, length of wing and
shape of leaflet, respectively. The ordination of the
species based on PCA is also compatible highly with
the related phenogram (Fig. 1).
In order to study relationship among the species
based on pollen morphology, (Figs. 4-9) the cluster
analysis under Ward method and based on understudied
characters was performed and the result is delineated in
Fig. 2. According to this phenogram, in the linkage
distance 12, two main clusters are observed. The first
cluster includes two subclusters 1 and 2. In the first
subcluster, C. bijugum from the section Monocicer is
Table 2. Cicer species, their localities and voucher numbers in pollen study.
Species
Locality
IRAN. JOURN. BOT. 12 (2), 2006
151 Cicer morphology
Section 1: Monocicer
C. arietinum L.
C. bijugum Rech. f.
Section 2: Chamaecicer
C. chorassanicum (Bge.) M.
Pop.
C. incisum (Willd.) K. Maly.
Section 3: Polycicer
C. anatolicum Alef.
C. kermanense Bornm.
C. spiroceras Jaub.& Spach
C. oxyodon Boiss. & Hoh.
C. subaphyllum Boiss.
Section 4: Acanthocicer
C. stapfianum Rech. f.
C. tragacanthoides Jaub. &
Spach
Var. tragacanthoides
var. turcomanicum M. Pop.
Tehran: Karaj, farm of Genebank 1321m, Mesbah & Roohnavaz 1400.
Kermanshah: Gahvareh, 5 km. E. of Changar, 1880m, Jalilian et al. 1402.
Khorasan: Esfaraien to Sabzevar, 5-20 km Sabzevar, Termeh 39956-E.
Lorestan: Oshtoran kouh, Ghaleh Rostam to Gahar, 2400-2700m, Iranshahr 14626.
Hamadan: Gardaneh Asadabad , Galehbour, 2250, Kalvandi et al. 1403.
Kerman: Baft, Siah kouh, Hamzehnejad H-1529.
Bakhtiari: Ardal, Sarhang Mahmoud, 1800m, Iranshahr & Moussavi 39966-E.
Tehran : Shahrestanac, 2300m, Pakravan 1408.
Fars: Shiraz, near Marvdasht, Kouh – e- Ayyoub, 2100m, Neamati & Jalilian 1412.
Fars: Shiraz, Eghlid, Kouh-e-Bel, Sardab, 2900m, Jalilian et al . 1413.
Semnan: Shahroud , Gharieh-e-Tash to Kouh-e-Shahvar, 2600-3300m, Moussavi
& Karavar 33605-E.
Khorasan: Kopet Dagh, 45km N.N.E of Shirvan, Kouh-e-Alam, 2400m, Edmonson
26921-E.
Table 3. Cicer species, their localities and voucher numbers in seed study.
Spicies
Locality
Section 1: Monocicer
C. arietinum L.
Azerbaijan: Tabriz, Benis, Jalilian 1401.
C. bijugum Rech. f.
Kermanshah: Gahvareh, 5 km. E. Changar, 1880m, Jalilian et al 1402.
Section 2: Chamaecicer
C. chorassanicum (Bge.) M. Khorasan: Esfaraien to Sabzevar, 5-20 km Sabzevar, Termeh 39956-E.
Pop.
C. incisum (Willd.) K. Maly. Lorestan: Oshtoran kouh, Ghaleh Rostam to Gahar, 2400-2700m, Iranshahr 14626.
Section 3: Polycicer
C. anatolicum Alef.
Hamadan: Gardaneh Asadabad, Galehbour, 2250, Kalvandi et al. 1403.
C. kermanense Bornm.
Kerman: Mahan, Darreh-e-Kahnouj, Farhani 1411.
C. spiroceras Jaub. & Spach Bakhtiari: Ardal, Sarhang Mahmoud, 1800m, Iranshahr & Moussavi 39966-E.
C. oxyodon Boiss. & Hoh.
Ghazvin: Alamout 2300-2400m, Farhani 1404-A.
C. subaphyllum Boiss.
Fars: Shiraz, near Marvdasht, Kouh – e Ayyoub, 2100m, Neamati & Jalilian 1412.
Section 4: Acanthocicer
C. stapfianum Rech. f.
Fars: Shiraz, Eghlid, Kouh-e-Bel, Sardab, 1900m, Jalilian et al . 1413.
C. tragacanthoides Jaub. &
Spach
var. tragacanthoides
Semnan: Damghan to Shahroud, Gharieh-e-Tazareh, Kouh-e-Sefid-Shekar, 27003000, Moussavi & Karavar 33590E.
var. turcomanicum M. Pop.
Khorasan: Kopet Dagh, 45km N. N. E of Shirvan, Kouh-e-Alam, 2400m,
Edmondson 26921-E.
located near the species C. incisum and C.
chorassanicum from the section Chamaecicer which
they are nearly incompatible with the morphological
phenogram. In the second subcluster, the species C.
subaphyllum from the section Polycicer is located close
to C. tragacanthoides var. turcomanicum, belonging to
the section Acanthocicer. And the two species C.
stapfianum
and
C.
tragacanthoides,
var.
tragacanthoides from the section Acanthocicer are
located close to each other, as well. These species
which belong to the two mentioned sections are located
near together according to the classic classification.
IRAN. JOURN. BOT. 12 (2), 2006
Sharifnia & al. 152
Fig. 1. Phenogram and ordination based on morphological data of Cicer species. –Abbreviations, inc= C.
incisum; cho= C. chorassanicum; ari= C. arietimum; bij = C. bijugum, ker= C. kermanense; spi= C.
spiroceras; ana= C. anatolicum; oxy= C. oxyodon; var. tra= C. tragacanthoides, var. tragacanthoides,
var. tur=C. tragacanthoides var. turcomanicum; s.c= subcluster
153 Cicer morphology
IRAN. JOURN. BOT. 12 (2), 2006
Fig. 2. Phenogram and ordination based on palynological data of Cicer species. Abbreviation as in fig. 1
IRAN. JOURN. BOT. 12 (2), 2006
Sharifnia & al. 154
Fig. 3. Phenogram and ordination based on seed characters of Cicer species. Abbreviation as in fig. 1
155 Cicer morphology
IRAN. JOURN. BOT. 12 (2), 2006
Fig. 4. A. Pollen grains of Cicer species. 1-3. Cicer arietinum, 1) Equatorial view (x 1300), 2) Polar view (x 2000),
3) Ornamentation (x 4000); 4-6. Cicer bijugum, 4) Equatorial view (x 2000), 5) Polar view (1300), 6)
Ornamentation (x 1400).
IRAN. JOURN. BOT. 12 (2), 2006
Sharifnia & al. 156
Fig. 5. Pollen grains of Cicer species. 7-9. Cicer chorassanicum, 7) Equatorial view (x 2000), 8) Polar view (x
2000), 9) Ornamentation (x 4000); 10-12. Cicer anatolicum, 10) Equatorial view (x 1300), 11) Polar view (x 1800),
12) Ornamentation (x 4300).
157 Cicer morphology
IRAN. JOURN. BOT. 12 (2), 2006
Therefore, pollen morphology phenogram also
confirm this similarity. The second cluster is also
consisted of two subclusters (subclusters 1 and 2 ). The
first subcluster, consists of C. anatolicum, C.
spiroceras, and C. oxyodon from the section Polycicer,
and also the 2nd subcluster including C. arietinum from
the section Monocicer are located near the species C.
kermanense from the section Polycicer. According to
the table of morphological characters of pollen (table
4), these two latter species, in spite that they belong to
separate sections but have similar pollen specifications
including similarity in equatorial view, polar view,
colpi position and length of them. Therefore, these two
species are isolated from the other related species of
sections in terms of pollen specifications, and this
status does not confirm the classic classification. With
regard to the results obtained, we observed that two
taxa of C. kermanense and C. spiroceras are different
in all pollen specifications, as it was true for
differences in morphological specifications. Therefore,
it validates the distinction of them as two separate
species.
Meanwhile, in this phenogram similar to
morphological phenogram C. subaphyllum appears
isolated from other species of the section Polycicer
within the 2nd cluster, indicating that this species is
different from the other species of Polycicer section in
terms of pollen specifications. This is true as the
ornamentation of exin surface in C. subaphyllatum is
reticulate but, in the other 3 species of the section is
reticulate-areolate. Also, the shape of pollen in this
species is oblate–spheroidal and in the other 3 species
is prolate. PCA analysis was also carried out and the
most variable characters are: P/E ratio, length of polar
axis and shape of pollen grains.
Fig. 6. Pollen grains of Cicer oxyodon. 13) Equatorial
view (x 1500), 14) Polar view (x 2000), 15)
Ornamentation (x 4300).
The ordination of species based on PCA is also
comparable highly with the pollen morphological
phenogram (Fig. 2).
The seed morphology of Cicer species were studied
(Fig. G-L)
Cluster analysis using Ward method and based on
understudied seed characters was also carried out. The
result of this analysis is shown on phenogram 3.
According to this phenogram in the linkage distance 9,
two main clusters observed. The first, includes two
subclusters which in the first subcluster, two varieties
of C. tragacanthoides are observed. As expected, they
are completely similar and are located near each other.
Near these two varieties C. spiroceras belonging to
Polycicer section is located. Comparing to table 5, the
specifications keeping these 3 species belonging to two
different sections close to each other, are mainly seed
circular shape and after that seed coat texture and seed
color which are similar in high extent in these 3
species.
IRAN. JOURN. BOT. 12 (2), 2006
Sharifnia & al. 158
Fig. 7. Pollen grains of Cicer species. 16-18. Cicer kermanense, 16) Equatorial view (x 1300), 17) Ornamentation (x
3500), 18) Polar view (x 2000); 19-20. Cicer spiroceras, 19) Equatorial view (x 1300), 20) Ornamentation (x 4000).
159 Cicer morphology
IRAN. JOURN. BOT. 12 (2), 2006
Fig. 8. Pollen grains of Cicer species. 21-23. Cicer Subaphyllum, 21) Equatorial view (x 2000) 22) Polar view (x
1800), 23) Ornamentation (x 4000). 24-26. Cicer stapfianum, 24) Equatorial view (x 1300), 25) Polar view (x 2200),
26) Ornamentation (x 4100)
IRAN. JOURN. BOT. 12 (2), 2006
Fig. 9. Pollen grains of Cicer species. 27-29. Cicer tragacanthoides, var.
Sharifnia & al. 160