• 検索結果がありません。

Some Nigerian Species

N/A
N/A
Protected

Academic year: 2021

シェア "Some Nigerian Species"

Copied!
6
0
0

読み込み中.... (全文を見る)

全文

(1)

The Japanese Society for Plant Systematics

The JapaneseSociety forPlant Systematics

ISSN OOOI-6799 Acta Phytotax. Geobot. 47 (1): 41-46 (1996)

Cuticular Studies

of

Some Nigerian Species

of

Senna Tourn. ex Mill. (Syn. Cassia Tourn. ex L.):

Leguminosae-Caesalpinioideae

H. O, EDEOGA

and

PATRICIA I. OSAWE

Dqpartment

ofBotany,

Edo StateUhivens'ity,P.M. B.I4,Ekpoma, Edo

State,

Nigeria

Abstract. A comparative study of theleafepidermis of fiveNigerian

leguminous

species

has been done

using the"light microscope. Some of the cHfferences reeorded inthe epidermal cell walt architecture, trichomes, size, distribution,frequency and morphology of the stomatal complex havc been discussedinlinewith theirtaxonomic significance.

The

nature of the uni- cellular andi multicellular

uichomes

are

described for

the

first

tirneinthese species of Senna,

and S.hirstttaisdiagnostic

in

acquisition of these two types of trichomes, The stomatal index

varied

from 47.1 % (S.

spectabilis) to

98.2 % (S.

alata).

Key

Words:

leaf,

Legumono$ae, Senna,triehome ReceivedOctober 27,1995;accq)ted May

Z

I996

According to Airy Shaw (1973), Senna Tourn,

ex

Mill. (Syn. Cassia

Tourn.

ex

L.) is

a

large genus

of about

600

species

distrjbuted in tropical

and warm

temperate

regions of

the

world.

There

are about

22 indigenous

species and some aliens

in West Africa

which are used

for

medicinal and

decorative purposes.

Morphological features

of some species of

Senna including S.

aiata

(L.)

Roxb.; S. hirsuta (L.) H. S. Irwin & Bameby, S.

occidentalis

Link., S.

obtusijblia

(L.) H, S. Irwin & Barneby

and

S. spectabilis (DC.) I-I. S,

Irwin & Barneby have been described by Hutchinson and Dalziel (1968)

and

Akobundu

and

Agyakwa (1987). The

stems are either cylindrical or

ribbed

and woody and

therefore

can support

themselves. The leaves

are

petioiate

and vary

in

shape

depending

on

the

species.

Many

workers

have demonstrated the

value

of

epidermal characteris-

tics in tracing the

relationship of

different taxa. They include Metcalfe

and

Chalk (1950), Stebbins

and

Khush (1961), Pa}iwal (1966),Cutler (1978),

Shah (1968, 1969, 1971), Shah

and

Gopal (1969), Dehgan (1980), Gill

et

al.

(1982), Gill

and

Karatela (1982, 1983, 1995), Edeoga (1991), Gill

and

Karatela (1983),

and

found that in

the mature epiderfnis of members of

the Asclepiadaceae, the

upper epidermal cells are mostly

hexagonal

with

anticlinal and

periclinal

walls.

Conversely the lower

epidermal cells are elongated and

their

walls are sinuous.

Similarly Edeoga (1991) described

the

epidermal cells of

two Costus

species: namely,

C.

cofl7r

Ker-Gawl,

and

C. Iucanusianus Braun-Blanq. & K. Schum.,

observing

that the

upper

(2)

42

Acta Phytotax. Geobot, Vol, 47

epidermal cells of

the leaf

of

C.

cofierare

hexagenal

and

their leaves

amphistomatic.

Some Cassia

species

have

now

been

changed

to Senna

species

(Lowe

and

Soladoye, 1990). Taxonomic

studies on wide

geographic basis

may show

that

a

particular taxon in

one country

is in fact the

same as another

name.

Such

studies may

indicate that

a

particular genus

should

be

split

into

more separate

genera,

as

Cassia has been divided into Cassia, Senna

and

Chamaecrista.

This

recent separation of

Senna

species

from Cassia

species shows

that there is

need

to

ascertain

the taxonomic

characters which are unique

to this

new

genus. As

a new

taxon, information

about

it is incomplete; thus it is

an attempt

to fi11 in the gap in

our

present knowledge that the present

work was carried out.

Materials and Methods

Mature

and

fresh leaves

of

the five Senna

species

(S. hirsuta, S.

obtu-

sijblia,

S.

alata,

S.

occidentlis and

S. spectabilis)

were collected

(Inamdar,

1968) from different parts

of southern

Nigeria. Samplings

were made

by

using

fresh leaves from plants in their

natural conditions. rlhese

do

not undergo any

form

of

deteriolation

since

the leaves

were succulent.

These

materials were used

for the

epidermal studies

fo11owing the

method of

Cut- ler (1978)

with slight modifications.

Epidermal peels

were stained with

1 %

ethanol safranin and

temporarily

mounted

in

aqueous

glycerine

solution.

The

slides were studied under a

tight

miscroscope and

photomicrographs

of

epidermal cells including stomata and trichomes taken

using

a Carlzeiss Jenaval

miscroscope

fitted

with

MF AKS 24 × 36

automatic camera.

Sto-

matal

index was also caiculated. For the terminology

used

in this study see

Metcalfe

and

Chalk (1950).

Observations

The

cuticular characters were very

important in

all

the Senna

species

investigated

and were summarized

in Table 1. The

epidermal cells of

these

Senna species were

varied

in shape and were either irregular or sinuous,

slightly sinuous and coarsely sinuous.

The

epidermal cells ranged

from pentagonal, hexagonal to polygonal,

Paracytic

stomata were observed

in

all

the

species

but Senna

alata and

S. spectabilis; the latter two

species

have both paracytic

and anisocytic sto-

mata

in the

upper epidermis

but

only

paracytic

stomata

in the lower

epidermis

(Fig. 1-9). Two

major

types

of

hairs

were observed

in this

genus:

unicellular and multicellular

trichomes (Fig. 10-12). S. hirsuta had

both

unicellular and multicellular

trichomes

while

S.

alata,

S.

occidentalis,

S.

obtusijiolia and

S. spectabilis possesses

unicellular

trichomes

only.

The

stomatal

distribution in both the

upper and

lower

epidermis was also observed

to be

significant.

Thus the

stomatal

index

varied

from 47.1

(3)

The Japanese Society for Plant Systematics

The JapaneseSoclety forPlant Systematics

June 1996 EDEOGA & OSAWE: Cuticular

studies

in Senna 43

FIGs. 1-4, 1

and

2.

Lower and upper epidermis of

Senna

obtuhijblia.

Stornata

are

paracytic

and the epidermal celLs are varied inshape

(

×

200).

3 and 4.Lower and upper epidermis of S. oc'(,identa-

lis.Stomata are

paracytic

and the epidermal cells polygonalor almost

irregular in

shape

(

×

200).

% in Senna spectabilis to 98.2 % in S.

alata.

Of great importance to

note

was

the

close range of

the

stomatal

indices in both the

upper and

lower

epidermis

in

all

the taxa

studied,

Discussion

Metcalfe

and

Chalk (l9SO) had

earlier

described the

aspects of mature

epidermis

in

a number of mature

plants including Senna. The

epidermal characteristics of

the five

species studied showed

that the

epidermal cell wall

patterns

were

straight, slightly sinuous,

or

coarsely

sinuous.

The de- gree

of sinuousity according

to Esau (1965) is

caused

by the degree

of

force exerted on the stomata in their

course of

development.

In the presently investigated taxa, the leaves

were observed

to be

amphistomatic.

The

stomatal

indices

were

higher

on

the lower

epidermis compared

to the

upper

surfaces. These species also showed the existence

of variable stomatal

types: paracytic

and anisocytic.

This did

not agree with

Metcalfe

and

Chalk)s (1950)

reports which

indicated that the

stomatal

types of all the species

were

paracytic. Paracytic

stomata were observed

in

all

the five

species studied;

in

addition,

Senna

alata and

S.

spectabilis

showed anisocytic stomatal

type.

Most

of

the

species studied

had high

stomatal

index

and

this had

ear-

lier been

reported

by Gill

and

Karatela (1985)

and

Gill

et al.

(1983) in

Asclepiadaceae

and

Leguminosae. All the five

species

investigated had

(4)

44 Acta Phytotax, Geobot, Vol, 47

FIGs.5-8. 5 and 6,Lower and upper epidermis et Senna hirsuta.Sromata are

paracytic

and the epidermal cells are sinuous inboth surfaces

(

× 125 and × 200. respectively). 7 and 8.Lowcr epidermis

in S.

atata alld

S.

spectabilis respectively.

Both

paracyticand anisocyetic stomata arc

presentand the epidermal ce}ls are polygonal

(

× 200),

[I/ABLE1.

Cuticular

characteristics of the Senna species studied

Character

Stomatalindex

(%)

S,atataS. occidentalis S.obtusijbliaS. hirszataS. spectabilis

Stomataltype

Shape ofepidermal cells

Trichome

Upper ;

87.3 Lower

=

98.2

Paracytic&

anisocvtic

"

Mostly hexagonal

Unicellular

58.166,1

Paracytic

Varied,hexa- gonaltopolygonal

Unicellular

72.692.S

Paracytic

Mostlypolygonal

Unicellular

61.168.4

Paracvtic

Polygonal

&

sinuous

Unicellular

47.150.1

?aracytic

& anisocytic

Polygonal

&

sinuous

Unicellular Rows of cells

per trichome

1

1

1

3 1

trichomes

on

the

abaxial surfaces of

the leaf but the

cell architecture

however differed. Thus they

were unicellular

in

all

the

species except

in S.

hins"ta

where

they

were

both

unicellular and multicellular

(Figs. 11

and

12). Similarly in

all

the

species

there

was one row of cell

per trichome

ex-

cept

in S. hinsuta

which

had

up

to three

rows,

This

observation was

in Iine

with

that

of earlier authors

that had

vividly exphasized

the taxonomic im-

(5)

The Japanese Society for Plant Systematics

The JapaneseSoclety forPlant Systematics

June 1996 EDEOGA & OSAWE: Cuticular

studies

in Senna 45

FIGs,9-12. 9.Upper epidermis of Senna spectahitis.Note the presence of

paracytic

ancl anisocytic stomata

(

×

200). Ie. Lower

cpidormis of

S.

alata showing a unicellular trichome

(

× 12S).11.

Lower epidermis of S.htrsutashowing unicellular trichomes

(

× 62.5).12.Lowcr epidcrinis of

S,

hirsuta

showing a multicellular trichome

(

× 62,5).

portance

of

trichomes in

making reliable

taxonomic

conclusions

(Metcalfe

and

Chalk, 1995; Stace, 1980; Edeoga, 1991; Nyawuame

and

Gill, 1991).

The possession

of

paracytic

and anisocytic stomata

brought to ]ight the

phylogenetic

relationship of

these Senna species. Inspite of this, S. hirsuta

and

S.

alam exhibited cuticular attributes

that

cou]d

be

used

in

separating

them from the

other

taxa investigated. Though the

recent separation of some of

these Senna

species

from Cassia is

still

being questioned by

some authors,

the

epidermal

features

seemed

to

support such move.

Despite this

support, more

investigations in

other

lines

of

taxonomic

reasonings could

be initiated

such as

phytochemistry

and cytology

in these taxa. This

will

go

a

long

way

in

clearing

the

confusions

in the taxonomy

of

these Senna

species.

References

Airy Shaw, H. K, 1973. J. C, Willis' Dictionary

of the

Flowering Plants

and

Ferns. 8th

ed.

Cambridge University Press, Cambridge.

Akobundu, I. O.

and

C.

W. Agyakwa. 1987, A

Handbook

of

West African Weeds. 521 pp.

International Institute

of

Tropical Agriculture, Ibadan,

Cutler, D, F, 1978. Applied Plant Anaromy. 103 pp. Longmans, London.

Dehgan, B. 1980, Application of epidermal morphology to taxonomic

delimitation

of the

genus Jatropha (Euphorbiaceae). Bot. J. Linn. Soc, 80; 258-270,

Edeoga, H, O. 1991, Comparative

inorphology of the

leaf

epidcrmis

in Costt{s

tij}er-C.

Iucanusianus (Costaceae)

complex and

its

systematic

importance,

Nig. Ann. Nat,

Sc.

1:

(6)

46 Acta

 

Phytotax .

 

Geobot . VoL

 

47

    25− 30,

Esau

 

K .1965.

 

Plant

 

Anatomy .

 

767

 

pp

 

John

 

Wiley

 

London ,

Gill,

 

L .

 

S

 and  

Y .

 

Y ,

 

Earatela.1982.

 

Epidemal

 structure  and  stomatal  ontogeny  

in

 some

    Nigerian

 

Cucurbitanceae .

 

Willdenowia

 

12

303 31   ,

       

and

      1983,

 

Stomatogenesis

 

in

 

leaves

 of 

Calotropis

 

procera

 

Ait .

 

f .( Ascle−

    piadaceae )

 

Feddes

 Repert

94

519− 524,

        

and

      1985 ,

 

Structure

 and  ontogeny  of stomata  

in

 the 

foliar

 organs  of

   

some  

Nigerian

 

Ca

ia

 species

( Leguminosae ).

 

Iselya

 

2( 3)

121− 127.

       

G .0 .

 

Olabanli

 and  

S.

 W

 H

 Husani

. 1982.

 

Studies

 on  the structural  variation

   

and  

distribution

 of stomata  

in

 some  

Niger {

an 

legumes .

 

W { lldenowia

 

12

87− 94 . Hutchinson ,

 

J

 and  

M .

 

J.

 

Dalziel. .

1968.

 

Flora

 of 

West

 

Tropical

 

Africa . 606

 

pp .

 

Crown    Agents

 for 

Overseas

 

Government

 and  

Admin {

stration

 

London ,

Inamdar ,

 

J,

 

A .1968,

 

Epidermal

 structure  and  stomata  ontogeny  

in

 some  

Polygonales

 and    

Centrospermae .

 

Ann .

 

Bot .33

541− 552 .

Lowe

 

J.

 and  

M .0 .

 

Soladaye . 1990 .

 

Some

 changes  and  corrections  to names  of 

Nigerian     plants

 and  Nigerian trees since the 

publication

 of 

Flora

 of 

West

 

Tropical

 

Africa.2nd    

ed

 

Nig ,

 

J .

 

Bot . 3

1− 24,

Metcalfe ,

 

C .

 

R .

 and  

L

 

Chalk .1950.

 

Anatomy

 of 

Dicotyledons . 1500

 

pp

 

Clarendon

 Press

    Oxford ,

Nyamwuame

 

H

 

G .

 K

 and  

L ,

 

S .

 

Gi11.1991,

 

Cuticular

 studies  of somc  

West

 

African

 spe

−.

   

cies of the 

Apocynaceae

 of medicinal  value

 

Feddes

 Repert

. 102

87− 104.

Paliwal

 

G .

 

S.1966.

 

Structure

 and  ontogeny  of stomata  

in

 some  

Acanthaceae ,

 

Phytomor −

   

phology

 

16

527− 532 .

Pant

 

D .

 

D .1965.

 

On

 the ontogeny  of stomata  and  other  

homologous

 structures

 

Plant

 

Sci.

    Ser

 

Allahabad

 

1

1 24 .

Rollins,

 

B .

 

C .1944.

 

Evidence

 

for

 natural  

hybridity

 

between

 

guayale ( Parthenium

 argenta

−    

tum

and  

Mariola

P .

 

incanum

 

Amer .

 J

 Bot

31:

93− 97.

Shah ,

 

G .

 

L .1968.

 

Development

 of  stomata  

in

 some  

Papilionaceae,

 

J,

 

Indian

 Bot

 

Soc ,47

    305− 310 ,

       

1969

・Stomatal

 ontogeny  of the vegetative  and 

floral

 organs  of 

Crotalaria ,

 

Ann .

    Bot . 33

553 − 556.

        1971.Structure

 and  

development

 of stomata  on the vegetative  and  

floral

 organs

   

ln some  members  of 

Caesalpinaceae .

 

Ann .

 

Bot .35

745− 759 .

       

and  

B .

 V

 

GopaL

 

1969.

 

Development

 of stQata 

in

 some  Papi

ionaceae,

 

Can .

 

J.

    Bot , 24

387 391 .

Stace,

 

C .

 

A .1980.

 

Plant

 

Taxonomy

 and  

Biosystematics , 279

 

pp .

 

Edward

 

Arnold

 

London . Stebbins

 

G ,

 

L

 and  

G .

 

S,

 

Khush .1961.

 

Variation

 

in

 the organisation  of  

the

 stomatal  com

−     plex

 

in

 the 

leaf

 epidermis  of monocotyledons  and  

its

 

bearing

 on  their 

phylogeny.

    Amer .

 

J .

 

Bot . 48

51 57 ,

摘 要

オ ガ

H .0 .・P .1. オ サ ウ

ナ イ

ジェ

リ ア

Senna

ワ ラ

イ 属 )(

科 ジ

ツ イ ラ 亜

数 種

表 皮 系

比 較 研 究

   

Senna (= ワ ラ

ツ メ

イ属

)(

科 ジ

ラ 亜 科) 5 種

表 皮 系

光 学

微 鏡

に よ り比

較 研 究

気 孔

形 態

て , そ れ

分 類 学 的 意 義

議 論

. ∫

単 細 胞

多 細 胞

毛 を も

の 種

区 別

さ れ る と が

明 か

さ れ

同 時

Senna

れ ら 二

が 初

録 さ れ た .

立 大

植 物 学 研 究 室

参照

関連したドキュメント

As we have anticipated, Theo- rem 4.1 of [11] ensures that each immersed minimal surface having properly embedded ends with finite total curvature that is in a neighbourhood of M k

Keywords: continuous time random walk, Brownian motion, collision time, skew Young tableaux, tandem queue.. AMS 2000 Subject Classification: Primary:

In this paper, we focus on the existence and some properties of disease-free and endemic equilibrium points of a SVEIRS model subject to an eventual constant regular vaccination

By considering the p-laplacian operator, we show the existence of a solution to the exterior (resp interior) free boundary problem with non constant Bernoulli free boundary

“rough” kernels. For further details, we refer the reader to [21]. Here we note one particular application.. Here we consider two important results: the multiplier theorems

Abstract The classical abelian invariants of a knot are the Alexander module, which is the first homology group of the the unique infinite cyclic covering space of S 3 − K ,

Our method of proof can also be used to recover the rational homotopy of L K(2) S 0 as well as the chromatic splitting conjecture at primes p > 3 [16]; we only need to use the

Subsequently, Xu [28] proved the blow up of solutions for the initial boundary value problem of (1.9) with critical initial energy and gave the sharp condition for global existence