The Petiolar Structure of Christella dentata (Forssk.) Brownsey & Jermy (Thelypteridaceae, Pteridophyta)
KAMINI SRIVASTAVA, M.Sc, D.Phil
Department of Botany,
Allahabad-211002
E-mail: versatilekamini@rediffmail.com
Received
Abstract
The
exomorphic and structural details of the petiole of Christella dentata, a
fern frequently grown in gardens and glass houses as an ornamental, are
illustrated here for the first time. The stipes
receive two separate vascular strands from the rhizome which fuse together to
form a single strand during their upward course.
Key words: Christella dentata, petiole
anatomy, vascular strand.
Introduction
Fern
taxonomists have long employed the characteristics of the rhizome, indusium,
sporangia and spores in their construction of the systematic treatments of
various fern taxa. Leaf characters like venation pattern, trichomes, epidermis
and ontogeny of stomata have also been utilized for taxonomic purposes.
Likewise, stipe characters have also proved to be of
great value (Bower 1914, 1926; Kato 1972; Ogura 1972; Lucansky
and White 1974; and Linn and Devol 1977, 1978).
However, the characteristics of the stipe still
remain to be studied in the case of a number of fern species, and especially of
the Indian forms. With this thought held firmly in mind, the author has chosen
to study the exomorphic and internal details of stipe
of Christella dentata.
Similar investigations for other species of Christella viz.C. cylindrothrix,
C. subpubescens and C. malabariensis have been made by Shankar
(1986).
Materials and methods
Plants
of C. dentata were obtained from the
fern house of the Botany Department of Allahabad University,
Observations
The
petiole of C.dentata is cylindrical.
On the adaxial side of the petiole there is a prominent groove running from the
base up to the tip where the first pinna is attached. The base of petiole is
usually covered by scales. The marginal cells of scales are provided with fine projections
(Fig. 3 C). In addition to simple scales,
elongated hairs with tapering ends are found (Fig. 3 B). In surface view of the petiole, epidermal cells appear
narrow and elongated and devoid of stomata (Fig. 3 A). In a transverse section of the petiole, epidermal cells throughout
their length appear small, thick walled, dark brown in colour and covered by
smooth and delicate hairs. The epidermis is followed by three or more layers of thick walled
cells followed by several layers of thin walled parenchymatous
cells which constitute the ground tissue (Fig. 2A; Plate 1 F). Microchemical tests reveal
that the entire ground tissue is made up of cellulosic
cells. Thin walled inner layers of cells usually have starch grains. The petiole
receives two widely separated vascular strands from the rhizome (Fig. 1A; Plate 1A). Each vascular strand
is enclosed by a single layered endodermis. The pericycle
is made up of thin walled cells, which are one to three layers in thickness.
The xylem is mesarch and surrounded by phloem. The
xylem is hippocampus-shaped and the two vascular strands appear slightly
elongated. The adaxial arms are comparatively more turned inwards and the two
vascular stands appear almost reniform in shape (Fig. 1A; Plate 1A). Soon after entering the stipe base, the two
separate vascular strands start coming closer to each other and get fused
somewhere near the middle of the petiole to form a single strand for further
upward course(Fig. 1C; Plate 1C).
During the merger of the two vascular strands first the endodermis, the pericycle and at still higher levels the two phloem and
xylem strands also join each other at their abaxial side (Fig.1D, E; Plate1 D,
E). The distal arms of xylem and phloem however remain as such. Thus, the
single vascular strand that resulted due to fusion of the two is almost ‘U’
shaped and free arms of xylem strands turned inwards more in the former as
compared to the latter (Fig. 1E; Plate
1E). Xylem consists of tracheids with protoxylem having annular or spiral thickenings and metaxylem with scalariform thickenings. Phloem consists of
sieve cells with occasional parenchyma (Fig.
2B; Plate 1B).
Conclusion and Discussion
The
petioles of C. dentata
show differences in their external as well as internal structure as compare to C. cylindrothrix,
C. subpubescens and C. malabariensis. Their bases are covered with scales
consisting of thin walled cells. The marginal cells of scales have blunt
projections in C. cylindrothrix
and C. malabariensis and pointed in C. subpubescens
and C. dentata.
Multicellular hairs are distributed through out the
petiole in all the three species except in C.
dentata. From the base of the petiole a very
shallow groove arises on their adaxial sides which gradually become obscure in
the apical portion of C. cylindrothrix. However, in C. subpubescens, C. malabariensis
and C. dentata
it remains prominent even in the apical region of the petiole. Stomata are
absent on the epidermal portion of petiole of C. dentata, C. cylindrothrix and C. subpubescens except in C.malabariensis. Petioles of all the four
species receive two widely separated vascular strands from rhizome. Each
vascular strand is enclosed by an outer endodermal
layer whose cells lack the characteristic casparian
thickenings

Figure 1. Christella dentata.
A. Diagrammatic transection of petiole at the base showing two vascular
strands; B.
One of the vascular strands in a magnified; C, D, E. Diagrammatic
transection of petiole at various levels showing
stages during fusion of the two strands.

Figure 2. Christella dentata.
A. A portion of epidermis and
cortex of petiole in a transaction; B. Structural
details of a vascular strand.

Figure 3. Christella dentata.
A. Surface view of epidermis; B. Hair
from the petiole surface; C. Scale from the petiole surface.

Plate 1. Christella dentata. A. Transection
of petiole at base showing two vascular strands; B. One of the two vascular strands in a
magnified; C,
D, E. Transection of petiole at various
levels showing stages during fusion of the two strands; F. A portion of epidermis and
cortex of petiole in a transaction.
References
BOWER, F. O.1914. Studies in the phylogeny of the filicales.1v. Blechnum and allied genera.
Ann Bot. 28:363-431.
BOWER, F. O.1926. The Ferns. vol.II.
KATO, M. 1972. The vascular structure and its taxonomic significance in the Athyriaceae. Acta Phytotax. Geobot. 25: 79-91.
OGURA, Y.O. 1972. Comparative Anatomy of
the Vegetative Organs of the Pteridophytes,
LUCANSKY, T.W. & WHITE, R.A. 1974. Comparative studies of the nodal and vascular anatomy in the neotropical Cyatheaceae, 3. Nodal and petiole patterns; Summary and conclusions. Amer. J. Bot. 61: 818-828.
LIN, B.L. & DEVOL, C.E. 1977.
The use of stipe characters in fern taxonomy
LIN, B.L. & DEVOL, C.E. 1978. The use of stipe characters in fern taxonomy II Taiwania.23:77-95.
SHANKER, R.1986. Morphotaxonomic
studies of some Pteridophytes. D.Phil.Thesis, Departement
of Botany, TheUniversity of
FOSTER, A.S. 1966.Morphology of anstoses
in the dichotomous venation of cercaeaster. Amer. J. Bot. 53:
588-599.
JOHANSEN, D.A. 1940. Plant Microtechnique.
Mc Graw Hill Co.
REEVE, R.M. 1951. Histochemical test for polyphenols in plants. Stain Technol.
26: 91-96.