Research Article
Hair morphology in Three Local Solanaceous Taxa
Ganguly S* and Das S
Graduate Student, Department of Botany, Ranaghat College, Ranaghat, Nadia, West Bengal, India
*Corresponding author:Sudarshan Ganguly, Department of Botany, Ranaghat College, Ranaghat, Nadia, West Bengal, India. E-mail Id: sudarshanganguly2001@gmail.com
Copyright: © Ganguly S, et al. 2024. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Article Information:Submission: 06/05/2024; Accepted: 03/07/2024; Published: 08/07/2024
Abstract
Hairs or indumentum are the unicellular or multicellular outgrowth of epidermal cells, commonly observed on plant surface including leaves, stems, fruits and different parts of flower. Single linear row or several rows of cells constitute multicellular hairs. It holds significant role in plant taxonomy, physiology, ecology, anatomy, systematic and stress response study. The family Solanaceae with large number of genera exhibited diverse types of hair or trichome or indumentums. With an objective to study hair design pattern in Solanaceae, three locally available plants were selected and epidermal hair morphology
were investigated. Following proper methodology in cleaning, peeling and observation, both vegetative and reproductive parts were prepared on glass slides. Plant parts like leaves, stems and floral parts were observed. Fairly widespread diversity were observed between three different plants and between parts of same plant. The hair styles ranged from glandular to non-glandular, unicellur, bicellular to multicellular, branched to un-branched and other variations stellate, stinging, strigose, hirsute, hispid types etc. which were found to be stable in different replicates. The similarities and dissimilarities among taxa regarding hair morphology can be used as a reference point for future systematic studies in the family Solanaceae.
Keywords:Hair Design; Morphological Investigation; Vegetative and Reproductive Parts; Solanaceae
Introduction
The Solanaceae Juss. commonly known as Potato family, is a
large angiosperm family consisting a large number of genera (~3500
species) throughout the world, mostly shrubs or herbs rarely lianes,
distributed mainly in the tropical and temperate regions [1,2].
In India, this family is represented by 88 species, belonging to 15
families. Most of the species are either wild or cultivated throughout
India and are chiefly found in Himalayan range, Southern and
Eastern India [3]. Commercial taxa like potato (Solanum tuberosum
L.), egg plant (Solanum melongena), tomato (Solanum lycopersicum
L.), chilies (Capsicum annum L.), tobacco (Nicotiana tabacum L.) and
Datura (Datura stramonium L.) are cultivated throughout India as
commercial purposes. Solanum verbascifolium L. a small Solanaceous
tree that is native to southern North America and northern South
America is also observed in India. Many members of the family are
used as medicinal plants. Belladonna is a homeopathic medicine from
Atropa belladonna L., is used as treatment of spasmodic cough and
bronchitis and helpful on respiratory problems. Similarly, Withania
somnifera L. or ‘Aswagandha’ is used as a stimulant, tonic and
treatment of sleep disorder [2,4,5].
Surfaces of various plant organs display impressive variation
in the origin, size, shape, location, and distribution of epidermal
projections [6]. Notable among these are the plant hairs: Unicellular
or multicellular appendages (hair-like structures) originating from
epidermal cells of various plant parts including leaves, stems and
flowers [7], and projecting out wards [6]. Plant hairs are distributed
almost universally in the plant kingdom and exhibit dramatic
variation in their morphology and density on plant surface. The use
of morphological and leaf epidermal features has been found to be of
immense interest in taxonomic research [8,9].
Plant hairs can be classified into glandular (presence of glandular
head) and non-glandular (absence of glandular head) [6]. Taxa of
family Solanaceae exhibited wide spread variation in surface hair
morphology [6,10]. Both glandular and non- glandular hairs are
found which can be classified into unicellular and multicellular
hair. Non-glandular unicellular hairs were found as multicellular
which can be further classified into branched and unbranched. Nonglandular
multicellular branched hairs are four types – stellate, peltate,
Candelabra, T- shaped and non-glandular multicellular unbranched
hairs are three types-, uniseriate, biseriate, multiseriate [9,11].
Increased attention has been paid regarding roles of plant epidermal
morphology in taxonomic evaluations and responsiveness of plants
to biotic as well as abiotic stressors. Considering the importance,
present study has been undertaken to document the epidermal hair
morphology in different vegetative and reproductive parts of three
common members of Solanaceae. It can provide a reference point
for future study on hair types and its use in determining systematic
position and ranking of Solanaceous members in Angiosperm.
Materials and Methods
The present investigation was done on three plants belonging to
the family Solanaceae.
Study Area:
Present study was conducted in the month of February-March
2023. Plants materials were collected from Santipur, Nadia, West
Bengal, India. The plants were the most abundant in the present study
area [Figure 1].Methodology
The collected plant samples were carefully cleaned (not with water,
just dust free) and each part (stem, leaf, flower, and fruit) of every plant
were observed under compound light microscope (10x). Both adaxial
(dorsal) and abaxial (ventral) side of fresh leaf samples (n =5 per side
per sample) were used. For the microscopic investigation the stems
of collected plants were cut in transverse section (T.S). Stems and leaf
surface were peeled whenever necessary. The mechanical scratching
method was followed for obtaining the peels. Epidermal peelings were
taken from both the upper and lower surfaces of the fresh leaves, using
a sharp razor blade. The peelings were then washed in distilled water
and the peelings were then mounted in 50% glycerine, sealed using
wax and observed under Microscope. Chemical pre-treatment was
not done in any case and staining was avoided to prevent any damage
or alteration of the hair types/style. Each of the three specimen parts
were studied in three different plants of same species. Photographs
of each sample were taken in triplicate and suitable one was selected.
Hair type identification was done following Reo (1971) and hand
book of terminology of plant indumentum [13].
Results
In the present study, epidermal characters of three members of
Solanaceae were analysed. Both vegetative and reproductive organs
are considered. Among the vegetative characters, hair styles of
dorsal and ventral leaf surface and stem surface were studied. The
reproductive parts included surface hairs of floral parts like sepals,
petals, anther lobes, filaments, ovary and fruits. The nature of hair
types of the three members of Solanaceae are given in the [Table 1].
Solanum torvum Sw.:
Characteristics stellate, non-glandular hairs present on stem
surface. Leaf epidermis is characterized by presence of large number of
noticeable strong stellate hairs with 8 projections on both adaxial and
abaxial surfaces, with lesser number of hairs on the dorsal side than
that in the abaxial surface [Figure 2a-d]. On both dorsal and ventral
side of sepals, stellate hairs at high density were found interspersed
with small glandular hairs. Lower numbers of hairs are present on
petal surfaces. Hairs were multiple and stellate on ovary wall but are
small and glandular on stigmatic surfaces [Figure 2e-i].Nicotiana plumbaginifoia Viv.:
Unbranched glandular hairs showing sparse distribution are
found present on adaxial surface of leaves and stems [Figure 3a-f].
The hairs are multicellular on stem surface.Brugmansia suaveolens (Humb. And Bonpl. Ex Willd.) Sweet:
Leaf upper epidermis was covered by bicellular finger hair while
lower epidermis was covered by multicellular finger hair [Figure 3g-i]. Hairs are non-glandular, un-branched with broad base and pointed curved apex (strigose type). On stem surfaces, multicellular,
finger-like hairs with pointed tips are also found [Figure 3j].Discussion
Implementation of epidermal hair morphology or indumentum
in plant taxonomy and systematics has become a growing trend
to solve taxonomic problems in at genus and species level.Being
very distinctive, easily noticeable and variable, the hair styles
can be correlated with other taxonomic features of the taxa
under investigation[14,15]. Hair styles have been considered as
one of the most dependable genetic traits in angiosperm family
Solanaceae[4,16-18].
In the present investigation, different hair structures were
observed under light microscope in three different taxa belonging to
the family Solanaceae. Stellate hairs occurred in leaves and stems of
S. torvum as also observed in previous studies [9,18]. Hair styles are
diverse in these three species ranging from glandular to non-glandular
to stellate with different morphology in plant parts, as partially
covered in an earlier study on leaf surface of S. melongena [19]. Leaf
epidermis in S. torvum is characterized by presence of large number
of noticeable strong stellate hairs with 8 arms on both adaxial and
abaxial surfaces, with lesser number of hairs on the dorsal side than
that in the abaxial surface. This is in accordance with earlier works on
S. torvum leaves in which Kumar et al. (2017) [20] reported variation
in number of arms in stellate hairs of Solanum spp. In another study,
large-sized stellate trichome in S. torvum was present in the lower
epidermis but the upper epidermis reportedly showed small stellate
hairs [9]. In the present investigation, on both dorsal and ventral side
of sepals, dense stellate non-glandular hairs were found intermixed
with small glandular hairs. Lower numbers of hairs are present on
petal surfaces. Hairs were multiple and stellate on ovary wall but are
small and glandular on stigmatic surfaces. The thick mat provided by
stellate hairs in the present study may be correlated with ecological and
protective adaptation of Solanaceous members. Sampaio et al. (2014)
[5] observed great diversity of stellate trichomes, mainly porrectstellate
and multiangulate, and peltatetrichomes in S. swartzianum
Figure 1:Study area.
• Plant materials
A mixture of two wild and one domesticated species of genus Solanum were included in the present study. The selected plants are-
(i) Solanum torvum Sw.
(ii) Nicotiana plumbaginifoia Viv.
(iii) Brugmansia suaveolens (Humb. & Bonpl. Ex Willd.) Sweet
Selected plant specimens were identified with the help of Herbarium available at Department of Botany, Ranaghat College and author citation was done with
www.ipni.org.
Figure 2:S. torvum surface hair types; (a) adaxial, (b) abaxial surface of leaf, (c) petal, (d) stem, (e) glandular hairs on sepals, (f) mixed glandular and stellate hair
on sepals, (g) short glandular hair on ovary, (h) stalked stellate hair with 4 arms, (i) short glandular hair on stigma (10x).
Figure 3:Nicotiana plumbaginifolia: (a) multicellular long glandularhairs on adaxial leaf surface, (b) on abaxial surface, (c) on stem, (d) non-glandular scabrous hair on stem small pilose like hairs on sepals, (f) glandular hairs on anther filament; (10x) Brugmensia sp: Hair style on (g, h, i, j) leaf adaxial and abaxial surface, (k) Stemshair;(l) sepal abaxial surface; (m,n,o) petal abaxial and adaxial surface;(10x).
at Atlantic forest. Along with other leaf epidermal characters, the
study showed diversity of trichomes exhibiting four types: glandular,
nonglandular, stellate, and dendritic. Nonglandular trichomes were
found in the leaves of Hyoscyamus species, as found in the present S.
torvum, Brugmensia sp. But the pattern and intermixing with other
types of hairs on a particular plant parts are unique in the present
study which assumes significance for the future work.
The distinct stellate hairs in the present investigation also
exhibited glandular types which were found in the sepals and
stigma of S. torvum and also in sepals, anther filament, fruit surface
and adaxial surface of leaves and stems of N. plumbaginifolia. The
glandular hairs are multicellular in most of the cases and were
considered characteristics features of Solanum sp [20]. Lower
frequency of glandular hair compared to non-glandular unbranched
as well as dendroid-stelliform hairs was reported earlier in Physalis sp.
of Solanaceae [15]. Four types of trichomes (glandular, non-glandular
dendritic, non-glandular bicellular and non-glandular multicellular)
was reported, found in Withania somnifera [21], which in agreement
with the present study indicating occurrence of intraspecific variation
in epidermal hair styles in Solanaceous taxa.
A different type of hair pattern was observed in Brugmansia
suaveolens where upper epidermis of leaves was covered by bicellular
finger hair but lower epidermis was covered by multicellular finger
hair. Similar results were obtained earlier [9]. On stem surfaces,
multicellular, finger-like hairs with pointed tips are also found.
Present result supports earlier studies where multicellular finger
hairs were the major trichome type in Solanaceous members with the
exception of Capsicum sp. showing bicellular finger hair [9]. Absence
of glandular hairs/trichomes was also reported in leaves of Egyptian
collection of S. nigrum [22]. Besides, non-glandular and scabrous
types of hairs were also screened in species of Solanum and Nicotiana.
Many non-glandular hair or trichome types exhibit xeromorphic
nature and prevent apoplastic water leakage [23]. Quite contrastingly,
glandular trichomes may not cause physical damage as it is pliable but
can release toxic chemicals to intoxicate herbivores [24,25]. Glas et al.
(2012) [26] reviewed the metabolic diversity found especially within
glandular trichomes of the Solanaceae, and of the genomic tools like
targeted genetic engineering, available to manipulate their activities
for increasing pest resistance in sustainable agriculture.
Conclusion
Future Prospects:
Variety of hairs or trichomes can be considered as a measure
of evolutionary progress of the plant species. In plant science
hair style is a genetically-controlled morphology of plants. In the
present study, diverse types of hair styles were revealed; unicellular,
bicellular, multicellular, un-branched, branched, glandular, nonglandular,
scabrous, sessile, stalked, strigose and stellate types with
non-glandular types in higher frequency as compared to glandular
one. Both glandular and non-glandular hairs were noticed in the
three taxa and diversity of hair styles exists in number, distribution
pattern, and structure of hairs in three species. Seithe and Sullivan
(1990) [15] stressed the importance non-glandular stellate-dendritic
hair in taxonomic assemblage and grouping of solanaceous members
like Physalis. An evolutionary trend from unbranched to branched,
glandular to non glandular, non stalked /sessile to stalked, and few
to many branches has been proposed [27]. Among the hair styles,
stellate, non-glandular types were found in the members who did not
show huge glandular types and vice-versa, indicating distinct hair
types in Solanaceae. The similarities and dissimilarities among three
taxa regarding epidermal hair characters can be used as a reference
of future taxonomic grouping of taxa in Solanaceae. Furthermore,
being an important stressor, hairs in Solanaceae can also act as
referral source for further studies regarding hair-related traits and
their relationships with biotic and abiotic stresses. Use of advanced
genomic analysis and breeding tools on hair structure of Solanaceae
may give further information of biological significance of hair pattern
studied in the present Solanaceous taxa.Acknowledgements
Authors want to convey their sincere gratitude to Department of
Botany, Ranaghat College, Ranaghat, India for providing necessary
infrastructural facilities required in the present study.