Greener Journal of Biological Sciences Vol. 10(1), pp. 21-26, 2020 ISSN: 2276-7762 Copyright ©2020, the
copyright of this article is retained by the author(s) |
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Taxonomic
Studies on Telfairia occidentalis
Hooker (Cucurbitaceae)
*1Wahua,
Chika; 2Eke, Redeem Chinazam; 3Nichodemus,
Cornelius Onyidikachi
*1Department
of Plant Science and Biotechnology, Faculty of Science, University of Port
Harcourt, Choba, P.M.B.5323, NIGERIA.
*Email: chika.wahua@ uniport.edu. ng, Phone number: +2348064043448
2 Department of Plant
Science and Biotechnology, Faculty of Science, University of Port Harcourt, Choba, P.M.B. 5323, NIGERIA. Email: redeemeke8@ gmail. com
3 Department of Plant
Science and Biotechnology, Faculty of Science, University of Port Harcourt, Choba, P.M.B. 5323, NIGERIA. Email: cornel4nic@ gmail. com
ARTICLE INFO |
ABSTRACT |
Article
No.: 020120021 Type: Research |
This study
examined the morphological, anatomical, cytological, phytochemical
characteristics of Telfairia occidentalis
(Fluted pumpkin) in the family Cucurbitaceae.
Observations of plant parts aided by measurements were done and these were
sectioned following Wahua’s method; root tips
squashed with FLP Orcein and qualitative
phytochemical analysis was carried out. T.
occidentalis
is a dioeciously perennial plant with stem up to 10m long and 3-5 palmately arranged leaflets. The fruit is pale green with
waxy deposit strongly ribbed and light yellow fibrous flesh with flattened
seeds. The flower is composed of male and female inflorescence. The epidermal
studies revealed glandular trichomes, oil glands
and anomocytic stomata with polar contiguous
stomata on the abaxial layer. The anatomical
studies showed various internal structures for the stem, midrib, root,
petiole and node with bicollateral vascular bundle
arrangements. Diploid chromosome number of 2n=22 was observed. Phytochemical
screening revealed presence of alkaloids, flavonoids, tannins, saponins, terpenoids, phenols
and cardiac glycosides across the three extracts while steroids was absent. The
information generated from this study further aid the delimitation of the
species. |
Accepted: 02/02/2020 Published: 25/02/2020 |
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*Corresponding
Author Wahua,
Chika E-mail:
chika.wahua@ uniport.edu.ng Phone:
+2348064043448 |
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Keywords: |
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INTRODUCTION
The genus Telfairia Hooker belongs to the
family Cucurbitaceae and contains two (2) species in
Africa namely; Telfairia occidentalis Hooker
and T. pedata
(Sm. ex Sims.) Hooker from West Africa and East Africa
respectively (Okoli, 2013). Although T. occidentalis
is an herbaceous perennial plant, it is grown as an annual crop due to its
importance in parts of West Africa (Irvine, 1969). In Nigeria, Telfairia occidentalis
is extensively cultivated in the southern part by the Igbos where it is fast
becoming an important vegetable crop (Okoli, 2013)
and has become a major component of their diets and can be found in every home.
In trado-medicine, it is used as blood booster, improve immune system, aid digestion and convulsion
(Kayode et al., 2010).
The antioxidant
property of T. occidentalis
has been widely reported by several authors (Nwanna
and Oboh, 2007; Eseyin et
al., 2014; Eseyin et al., 2018). Nutritionally, this
leafy vegetable is rich in minerals such as iron, potassium, sodium,
phosphorus, calcium and magnesium and some essential amino acids (Fasuyi and Nonyerem, 2007). Major
Phytochemicals present include; tannins, saponins, flavanoids and phenolics (Ekpenyong et al., 2012; Adeniyi
et al., 2010).
Some taxonomic lines
of evidence have been explored in the study of T. occidentalis such as morphology (Hutchinson
and Dalziel, 1954), phytochemistry
(Adeniyi et al., 2010), cytology (Okoli
and Mgbeogwu, 1983).
This present study examines the morphology,
anatomy, cytology and phytochemistry of T. occidentalis
to further provide useful taxonomic information relevant to its identification
and delimitation.
MATERIALS AND METHODS
Morphological Studies
Observations of the morphological characters (vegetative
and floral) were made and a meter rule was employed to aid their measurements.
The seeds were obtained from Rumuokoro market in Port
Harcourt while the plant parts were collected from University of Port Harcourt
farm, Rivers State, Nigeria.
Anatomical Studies
Fresh plant parts (stem, midrib, petiole,
node and roots) collected were fixed in FAA solution (in the ratio of 1:1:18)
for 48 hours, Johansen (1940) with some modifications, and later subjected to
free hand sectioning using 5 blades as described by Wahua
(2013) with 2 sets (Nacet and Tiger blades) crossed
and a central vertical one (Nacet) lying in between
the 2 sets crossed. The blades were adjusted until the holes in them synchronized.
The plant part to be sectioned was placed in the hole and using the first two
fingers of the left hand to hold the vertical blade sets, while pressing down
the 2 crossed sets with the first two fingers of the right hand to make a
transverse section of about 15 to 25µm in thickness. These were dehydrated in
ethanol solution of 30%, 50%, 70% and absolute for 5 minutes in each and
further passed through different series of alcohol and chloroform (3:1, 1:1 and
1:3) v/v for 10 minutes in each. Good sections were selected, stained with 1% Alcian blue, rinsed and counter stained with 1% Safranin 0 for 2 minutes. Mounted on glass slides with a
drop of glycerol and viewed under the microscope. Microphotographs were taken
(Metcalfe and Chalk, 1979; Stace, 1980).
Cytological Studies
The seeds were plated
in petri-dishes and allowed to grow roots. The roots were harvested at time
intervals (8, 9, 10, 11 and 12), dipped in 8 hydroxylquinoline
for 3hours removed and dipped in Carnoy’s fluid for
24hours (Okoli and Mgbeogwu,
1983). The roots were removed and dehydrated in water. 8% HCl was added in
a water bath and heated to 60o, the roots
were added to the boiling HCl and allowed for
4minutes to hydrolyze. The roots were removed and placed in 70% ethanol for 10minutes
to neutralize the acid. The root tip was placed on a glass slide and cut at 0.2cm, FLP Orcein was added,
covered with a cover slip and quashed. Air bubbles and excess stain were
removed using filter paper. The slide was viewed under the microscope for
observations and chromosomal counts with clear microphotographs taken from good
preparations.
Phytochemical Studies
Qualitative analysis
was carried out as described by Trease and Evans
(1989) and Sofowora (1993). The leaves of Telfairia occidentalis were screened for the presence of
flavonoids, tannins, alkaloids, terpenoids, saponins, steroids, phenols and cardiac glycosides.
RESULTS AND
DISCUSSION
Morphological Studies
Telfairia occidentalis (fig
1) is a perennial herb, grows up to 10m in length with leafs composed of about
3-5 palmately arranged leaflets, absence of stipules,
the petiole length is about 5-12cm with petiolules of
1.4-3.2cm long. The terminal or central leaflet is the largest usually up to
14-18cm X 8-11cm. The leaf margin is dentate with acute leaf apex and base. The
fruit is pale green, large, ellipsoid, strongly ribbed at maturity and about
35-50cm X 18-25cm with weight up to 3-6kg. The flower is composed of male
racemes about 13cm in length with lobe calyx while corolla is obovate and lobe. The seeds are flattened, yellow and about
3.5cm in diameter. Taxonomic studies of plants provide useful and diagnostic
information required for the identification and classification. This work
explored four (4) basic lines of evidence namely; morphology, anatomy, cytology
and phytochemistry and each proved very important to
this study. Morphological investigation of T.
occidentalis having palmate leaves (trifoliate),
climbing stem, white to purple flowers and pale green fruit corresponds to the
findings of Hutchinson and Dalziel (1954) and Okoli (2013). The measurements for the fruit size and
weight were similar to the results obtained by Tindall
(1983).
Fig
1. Morphology of T. occidentalis
(A) Habit (B) Flower (C) Tendril (D) Fruit
Anatomical Studies
The stem anatomy (fig 2A) revealed 1
epidermal layer followed by 4-5 layers of parenchymatous
cortex with presence of non-glandular trichomes on
the epidermis. The vascular bundles are bicollateral,
eleven (11) and arranged in a ring form. Pericycle
cells surrounded the vascular bundles and pith at the innermost layer. The
midrib anatomy shows presence of non-glandular trichomes
on the epidermis, 1 epidermal layer, bicollateral
vascular bundles and layers of parenchymateous
cortex. The root anatomy shows presence of parenchyma cells, absence of pith
and thick walled intercellular spaces. In the petiole anatomy, it revealed a
well curved bicollateral vascular bundle. Presence of non-glandular trichomes on
the epidermis with 1 epidermal layer with layers of parenchyma cells.
The nodal section revealed the presence of 1 epidermal layer, curved vascular
bundle and numerous parenchyma cells as shown in fig 2E. The anatomical study
further gave an insight into the internal structures by highlighting basic
components which distinguishes T. occidentalis from other plant species. The curved
arrangements of the bicollateral vascular bundles in
the petiole agreed with the reports of Okoli (1987).
The epidermal characteristics showed clearly that anomocytic
stomata is the dominant stomata type in T. occidentalis
and contiguous stomata, only in the adaxial layer. Peltate gland of 5 parts (pentagon) observed only in the adaxial layer provided diagnostic tools relevant to this
study.
Fig
2. Transverse section
of T. occidentalis
(A) Stem (B) Midrib (C) Root (D) Petiole (E) Node
Vb
represents vascular bundle, P represents pith, Pc is parenchymatous
cortex, Pe is pericycle,
NGT is non glandular trichome,
INS is xylem vessel, E represents epidermal layer.
Epidermal studies
Telfairia occidentalis
is amphistomatic (fig 3). The adaxial
layer contains anomocytic stomata with 5 subsidiary
cells and peltate glands of 5 parts (pentagon). The
epidermal cell shape is irregular while the anticlinal cell wall pattern is
regular. The abaxial layer contains anomocytic stomata with 4, 5 and 6 subsidiary cells and tetracytic stomata. Contiguous stomata (polar) phenomenon was
observed randomly in the abaxial layer. The epidermal
cell shape was irregular while the anticlinal cell wall pattern was wavy.
Fig
3. Epidermal layers of T. occidentalis
(A) Adaxial layer, (B) Abaxial
layer arrow revealed contiguous stomata.
Cytogical Studies
A diploid chromosome number of 2n=22 was
observed in T. occidentalis as shown in fig. 4. The
basic chromosome number of T. occidentalis n=11 as reported by Okoli
and Mgbeogwu (1983) was confirmed in this study. This
shows that the species has diploid chromosome number 2n = 2x = 22 with the
chromosome size relatively different.
Fig
4. Chromosomes of T. occidentalis
Phytochemical Studies
The phytochemical results using three
different extracts revealed the presence of various metabolites and their
relative compatibility to the extracts (methanol, ethanol and aqueous). Saponins, alkaloids and flavonoids were present in the
three extracts, terpenoids only present using ethanol
extract but absent in others. Phenols were present in methanol and aqueous
extracts but absent in ethanol extract. Cardiac glycosides were present using
methanol and ethanol extracts but absent using aqueous extracts. Steroids were
observed to be absent in all the extracts. These findings were in accordance
with the reports of Ekpenyong et al. (2012) and Adeniyi et al. (2010). The level of phytochemicals present
further reveals the reason for its high ethnobotanical
potentials and usage in treatment of various ailments.
Table 1. Showing the result of the
phytochemical screening
Phytoconstituent |
Methanol |
Ethanol |
Aqueous |
Alkaloids
|
+ |
+ |
+ |
Flavonoids
|
+ |
+ |
+ |
Saponins |
+ |
+ |
+ |
Terpenoids |
_ |
+ |
_ |
Steroids
|
_ |
_ |
_ |
Phenols
|
+ |
_ |
+ |
Cardiac
glycosides |
+ |
+ |
_ |
Key:
+= present; - = absent
CONCLUSION
It is worthy of note that the four taxonomic
lines of evidence employed in this work has further provided useful diagnostic
information required for the delimitation of the species.
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