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Chapter 3
Review of Literature
The literature pertinent to different aspects of the present study has been reviewed
and categorized under the following broad headings:
3.1 Inventorization of plant bioresource
3.2 Population structure of higher plants
3.3 Species distribution patterns
3.4 Phytosociological studies
3.5 Traditional knowledge on phytotherapy
3.6 Conservation implications
3.1 Inventorization of plant bioresource
The history of plant explorations in India is quite old. Over the time, a satisfactory
progress has been made across the country as far as inventorying of plant diversity is
concerned. Among the workers who have made significant contribution in exploring and
describing plant diversity in different parts of the country are Hooker (1872-1897) for the
entire Indian sub-continent, Cooke (1901-1906) for Mumbai, Brandis (1921) for Indian
trees, Naithani et al. (1997) for flora of Goa, Pullaiah and Ramamurthy (2001-2001) for
eastern Ghats, Parkinson (1923) for Andaman Islands, Shetty and Singh (1991-1993) for
Rajasthan, Parker (1984) for the Punjab region, Chaudhuri (1993) for eastern India, Hajra
and Verma (1996) for Sikkim, Kanji Lal (1991) for Assam, Duthie (1994) for the Upper
Gangatic Plains, Shiwalik and sub-Himalayan tracts. Nayar (1980) reported about 141
endemic genera in India, distributed over 47 families where Acanthaceae and Graminae
were recorded for the largest number of endemic genera (17 each). There have been
attempts by Jain and Roy (1983), Nayar and Sastry (1987-1990), Ved and Tandon (1998)
to assess floras on the basis of which many of the species found place in the Red Data
Book of Indian plants. Besides these, a few reference publications exclusively on the
medicinal plants are also available such as by Nadkarni (1908), Kirtikar and Basu (1916),
26
Gaur et al. (1983), Jain (1991), Jain and Filipps (1991), Chatterjee and Pakrashi (1997)
etc.
There has been a satisfactory progress towards inventorying plant diversity in
many parts of the Indian Himalayan region (IHR), with geographic distribution of the
plants. Polunin and Stainton (1984) gave an account on the flowers of the Himalaya
covering Jammu and Kashmir, Himachal Pradesh, Uttarakhand and adjoining areas upto
Nepal and Bhutan.
In central Himalaya, contribution of Aitchison (1864-89) in the study of flora of
Himalaya including Kumaun and Garhwal, Raizada and Saxena (1978) for Mussoorie,
Naithani (1984-85) of Chamoli, Osmaston (1994) for Kumaun, Rana et al. (2003) for
Tons valley and Gaur (2003) for the entire Garhwal Himalaya are significant. Rawal and
Dhar (1997) reported more than 64% of species as native Himalayan taxa out of total 465
species recorded in the timberline flora in a part of Kumaun. Scrophulariaceae (78%),
Ranunculaceae (70%), Asteraceae (69%), Rosaceae (68%), and Saxifragaceae (63%)
were the dominant families showing high percentage of native taxa. Samant and Dhar
(1997) also presented an inventory of over 675 wild edible plant species, representing
384 genera and 149 families. A total of 135 species have been reported from the
Panwalikantha alone which is situated at an elevation 3800 m (Nautiyal et al., 1997).
Joshi et al. (2000) explored Pindari area of Nanda Devi Biosphere Reserve and reported
224 plant species with their distribution and medicinal uses.
An account of the diversity in vegetation and flora of Tons valley in Garhwal
Himalaya covering 761 species of phanerogams belonging to 480 genera and 132
families has been compiled by Rana et al. (2001), however various life form categories
and biological spectrum of flora of Tons valley has also been reported (Rana et al., 2002).
Samant and Pal (2003) recorded 701 species of medicinal plants of which 138 species
were trees, 135 shrubs, 421 herbs and 7 species were ferns in various forest types of
Uttarakhand. In a floristic study on Nanda Devi Biosphere Reserve, Samant and Joshi
(2005) reported 490 species belonging to 281 genera and 89 families of angiosperms and
gymnosperms and categorized 37 species as critically endangered, endangered,
vulnerable and low risk near threatened using IUCN criteria.
In western Himalaya, Rau (1975) provided the taxonomic and distribution
information on flowering plants. In Jammu and Kashmir, the publications: flora of
27
Ladakh (Kachroo et al., 1977), Upper Liddar Valleys (Sharma and Jamwal, 1988) and
Srinagar (Singh and Kachroo, 1994) are noteworthy. From eastern Ladakh region of
Indian cold desert, Klimes (2003) also recorded a total 404 species of vascular plants.
Similar efforts in Himachal Pradesh started when Collet (1902) covered Shimla
area for the systematic study of its flora and later Chowdhery and Wadhwa (1984)
documented the plant biodiversity of the entire State. Besides these, flora of Bashahr
Himalaya (Nair, 1977) and Great Himalayan National Park (Singh and Rawat, 2000) are
also significant contribution in plant inventorization. In other local floral explorations,
Dhaliwal and Sharma (1999) presented an inventory of 930 plant species for Kullu
district, distributed among 504 genera belonging to 126 families and discussed their
taxonomic features thoroughly. However, many of the species from this district were also
mentioned in the publication of Chauhan (1999) who recorded 700 species of medicinal
and aromatic plants from Himachal Pradesh.
About 898 species of seed plants belonging to 544 genera distributed among 139
families have been reported in the flora of Sirmour district (Kaur and Sharma, 2004).
Singh and Sharma (2006) compiled the flora of Chamba district of Himachal Pradesh and
listed 1005 species of seed plants (545 genera and 133 families) with their
phytogeographical and ethnobotanical notes. Besides these, Subramani et al. (2007)
studied the floristic diversity of Renuka Wildlife Sanctuary in Sirmour and reported 395
species belonging to 316 genera and 115 families of which 228 species were medicinal
and aromatic in nature and 85 species were exotics.
Lahul-Spiti has been extensively explored since 1961, when Rau (1961)
conducted floristic surveys and reported 67 medicinal plants from the Lahaul valley.
Later Uniyal et al. (1973) and Aswal and Mehrotra (1987) highlighted the potential
medicinal plants of the entire Lahul Spiti and Lahul valley respectively. It was followed
by the publication of the flora of Lahaul-Spiti by Aswal and Mehrotra (1994) who
reported a total 985 species belonging to 353 genera and 79 families of angiosperms and
gymnosperms with their detail description. Kala (2006) also reported a total 335
medicinal plant species of which 45 were rare and endangered in high altitude cold desert
areas of Lahaul-Spiti including Ladakh.
28
3.2 Population structure of higher plants
Species diversity is an important indicator for the ecological and environmental
conditions of an ecosystem which provides the fundamentals to frame their management
as well as monitoring mechanisms. Studies on ecological niches and amplitudes of plant
species including identification and documentation of rare, threatened and endemic taxa
are important for the conservation of biodiversity (Varghese and Menon, 1999). In north
eastern region of the country, 98% of Indian species of Rhododendrons are found which
form a major plant group at upper temperate locations having a characteristic of slow
growth rate. Due to human interference, natural population of these species is gradually
diminishing due to deforestation and unsustainable extraction for fuel wood in the Sikkim
Himalaya (Singh et al., 2003). Similarly, Rai et al. (2000) highlighted conservation
threats to some important medicinal plants of this region.
In various efforts to assess the biodiversity in south India, Kadavul and
Parthasarathy (1999) while studying the tropical semi-evergreen forest in the Shervarayan
hills of Eastern Ghats, Ayyappan and Parthasarathy (1999) during biodiversity
inventorization of tropical evergreen forest in Varagalaiar, Anamalais and Kunte et al.
(1999) while studying the patterns of butterfly, bird and tree diversity in Western Ghats,
stressed upon to classify the landscape on the basis of structural vegetation types for
monitoring the status of bioresource and designing biodiversity conservation strategies.
Further, they found that quantitative measurements of abundance of plant species in
different landscape elements (LSE) types under various natural as well as human induced
threats/ pressures need to be carried out as the basis for any meaningful in situ and ex situ
conservation.
While studying the ecological status of reserve forests in Western Ghats, Swamy
et al. (2000) revealed significant variations in plant diversity and population structure in
these forests largely due to anthropogenic and other biotic factors. They reported species
diversity, density and basal area greater in the mid elevation forests than the low
elevation forests. Further, decrease in stem density and species diversity was recorded
with increased size classes of trees showing single species dominance in all the forests.
Substantial amount of work has also been carried out at regional and local levels
in various parts of Indian Himalayan region (IHR), which focuses on plant species
diversity in different ecosystems. However, quantitative information on the micro-habitat
29
preferences and population structure of various commercially important taxa is virtually
lacking from many parts the Himalaya (Kala, 2000; Uniyal et al., 2002).
In the mountainous region, particularly at high altitude areas, there are number of
constraints in the ecological assessment of plants which include toughness and
inaccessibility of the terrain, inhospitable climatic conditions, and limited period for
survey due to the short life cycle of plant species growing at such elevations (Kala,
2004). Despite of these facts, ecological studies on the distribution and population status
of plants in wild, along with population dynamics in various habitats/ landscape elements
(LSEs) are imperative to provide baseline information required for planning of
biodiversity conservation at the species and landscape level of a region.
Dhar et al. (2000) focused on the identified gaps in knowledge and lack of
objective assessment of threats which are considered a major drawback in setting
conservation priorities for Himalayan plant bioresource. Uniyal et al. (2002) believed that
excessive anthropogenic activities are the main cause of the decline in the population and
availability of various species of medicinal plants in nature. Keeping in view the
knowledge gaps and incomplete data, Kala (2004) reported that most of the available
information on various aspects of the plants in Himalayan region is collected from the
easily accessible areas in the mountains which are also accessed by the local people for
the collection of medicinal plants for indigenous use. Therefore, estimated population
density from such areas would definitely differ from the areas that have never or hardly
undergone any collection. Therefore, he reported that quantitative population estimates of
some of the threatened species like Dactylorhiza hatagirea and Picrorhiza kurrooa do
not focus to categorize these species critically endangered and endangered respectively in
IHR.
Significant information on the species diversity, composition and population
status of higher plants from central Himalaya, from the state of Uttarakhand in particular
has provided a number of quantitative estimates covering various characteristics from
species level to the landscape level. Singhal and Soni (1989) conducted a thorough
ecological study in eight different sites of Mossoorie, dominated mainly by Cedrus
deodara, Pinus roxburghii and Quercus leucotrichophora and reported the density of
these species between 1.9 and 6.4 trees per 100 m2. Agni et al. (2000) studied the
regeneration pattern and tree diversity in the forests of Kumaun and observed the absence
30
of young regeneration of all the important dominant species which showed the inability
of these forests to produce progenies due to repeated burning and severe biotic pressure,
by both wild and domestic animals.
Quantitative estimates on population density of Himalayan yew (Taxus baccata
Linn.) have been provided by Rikhari et al. (1998) and Purohit et al. (2001) in central
Himalaya. Former showed that population of seedlings and saplings was found to be
better in the moist and shady micro-sites at undisturbed locations, however later studied
the impact of bark removal on survival of T. baccata which is traditionally used for
preparing beverages locally called namkin chaey (tea), in preparation of local medicines
and wood as timber. They found that population of this species has been reduced to a
large extent due to its excessive collection in Nanda Devi Biosphere Reserve. Kharkwal
et al. (2005) gave an account of species composition of oak forests and reported
ecological structure and species composition of Kharsu oak (Quercus semicarpifolia
Smith) forest that was more complex as compared to Banj (Quercus leucotrichophora)
and Tilonj (Quercus floribunda) forests as the total number of species, genera and
families observed in Kharsu oak forest were higher than Bhanj and Tilonj oak forests.
In Kumaun, Airi et al. (1997) studied the population structure of Himalayan May
Apple (Podophyllum hexandrum Royle) in its natural habitats and reported a high total
density (21.80 to 94.73 plants/m2) in Kumaun Himalaya. They found that species
performed best in specific habitats (Quercus-Abies forest floor), at relatively low altitudes
and in acidic soils. Another study was conducted by Haleema et al. (2006) on the
distribution, frequency, abundance and density of P. hexandrum in Anatanag and
Srinagar districts of Kashmir Himalaya who reported low average population density
(1.13 individuals/100m2) and frequency (18.70%).
In upper Gori valley, Uniyal et al. (2002) estimated population status and biomass
availability of 14 threatened medicinal and aromatic plant species which are extracted
and traded from the higher altitudes of Kumaun Himalaya and reported the habitat
preferences of most of the threatened species which were usually found in distinct
landscape units or habitats.
Manjkhola and Dhar (2002) highlighted the fast decreasing population density of
Arnebia benthamii, a highly valuable medicinal plant in Indian Himalaya. Airi et al.
(2000) also reported the population dynamics of Nardostachys jatamansi, a critically
31
endangered taxon which is distributed in specialized habitats in the high altitudes of
Himalaya, ranging from 3000 to 5000 m above mean sea level. According to them,
dripping moss laden rocks (frequency: 40.7%, density: 15.9 individual/m2) and moist
boulders (frequency: 25.9% and density: 16.8 individuals/m2) were the most preferred
habitats of Nardostachys jatamansi in different sites in Kumaun area. Nautiyal et al.
(2003) studied the threat and vulnerable status of Nardostachys in different locations on
the basis of phytosociological analysis, density and relative dominance when compared
with other alpine species of Himalayan region.
During assessment of Jurinea dolomiaea Boiss. in different habitats at alpine
meadows of Kumaun Himalaya, Awasthi et al. (2003) found the highest density (27,215
individuals/ha), frequency (86%) and biomass (1,687 kg/ha) in undulating meadows,
however, the least values were recorded in rocky habitats.
Nautiyal et al. (2002) explored the natural habitats of Aconitum spp. (A. balfourii,
A. heterophyllum and A. violaceum) in Garhwal Himalaya in order to study their
population structure, and found that all three species were restricted to specific pockets
with very low population density. Based on population density and degree of constancy
used to assign threat categories, these plants were classified as endangered.
Bhatt et al. (2005) observed that population status of Dactylorhiza hatagirea in
protected areas was higher as compared to the unprotected sites, perhaps due to high
extraction and increased grazing pressure. Among various threatened plants, an account
on the population density, biomass and ecological features of Swertia chirayita, a
critically rare medicinal plant in central Himalaya has also been provided by Bhatt et al.
(2006).
In moist temperate forests of Himachal Pradesh, Singh and Kaushal (2006) gave
an account of density of Pinus wallichiana, Picea smithiana, Cedrus deodara, Abies
pindrow, Quercus leucotrichophora and Quercus semicarpifolia in Chamba district,
where Pinus wallichiana and Cedrus deodara were found over large areas occupying
majority of space in most of the study sites. During a quantitative assessment of
medicinal plants in Chhota Bhangal area of H.P., Uniyal et al. (2006a) reported the
population density of 8 medicinal plants including Aconitum heterophyllum, Bergenia
stracheyi, Heracleum candicans, Jurinea macrocephala, Picrorhiza kurrooa,
Podophyllum hexandrum, Rheum australe and Selinum tenuifolium.
32
Population structure of 23 rare and endangered medicinal plants in Spiti cold
desert of H.P. was studied by Kala (2000) who reported the highest density
(individuals/m2) for Picrorhiza kurrooa (70.6 ± 43) followed by Saussurea gnaphalodes
(48.0 ± 11). Recently in his significant contribution, Kala (2005c) reported population
status of threatened medicinal plants in different protected areas of Indian Himalaya
including Kibber Wildlife Sanctuary and Pin Valley National Park in Lahaul-Spiti district
of H.P., where density of 8 species in former and 19 species in later was recorded.
Further he found high density and number of threatened and rare medicinal plants in the
moist habitats. Among various species, Arnebia euchroma and Ephedra gerardiana were
found the most common threatened plants.
3.3 Species distribution patterns
Accuracy of floristic surveys and digitization of biodiversity for its documentation
is the prime objective at global, national and regional level. Floristic maps may serve to
understand species distribution pattern along the range of complex environmental
variables and such information will be of significance to predict their geographical
relocation (Vats and Singh, 2002). A number of ecological factors are responsible to
govern the distribution of various components of a forest landscape including trees,
shrubs and herbs. Singh and Singh (1986) reported that single species dominance is very
common in the forests of central Himalaya. The high-altitude Himalaya is characterized
by cold and arid climate with rich and varied biotic potential where vegetation
composition is considered as an appropriate indicator for delineating the high-altitude
zone.
Dhar (2002) observed that distribution patterns of floristic elements of high-
altitude Himalaya change sharply at the upper temperate region all across the Himalaya
and found shifts in compositional pattern in this zone where conifer, mixed, broadleaf
communities (Salix, Aesculus, Abies and Pinus) are replaced by pure conifer stands
(Cedrus, Taxus and Abies) in parts of trans and northwest Himalaya; mixed broadleaf
(Aesculus, Fraxinus, Rhododendron and Quercus) by evergreen oak and conifers
(Quercus semecarpifolia, Pinus and Abies) in the west and mixed broadleaf (Alnus,
Michelia, Castanopsis and Litsea) by oak and conifers (Quercus lamellosa, Abies and
Tsuga) in central and east Himalaya. However, high-altitude Himalaya is reported to
33
show decline in tree-species richness, total tree density, basal area and productivity
(Dhar, 2002).
Significant literature explaining the species distribution patterns in central
Himalayan region is available. Samant et al. (2001) reported that central Himalaya
supports rich plant diversity and they found maximum species diversity (46.22%) in
Kumaun and Garhwal Himalaya in the lower zone and the lowest (5.53%) in the upper
zone of 4001-5000 m elevation. In moist temperate forest of Kedarnath forest division,
species diversity index was invariably higher for herbs than of the shrubs and trees
(Pande et al., 2001).
Drastic change in vegetation due to ecological variables is a fundamental
characteristic of mountain ecosystems. Besides soil properties, altitude is one of the basic
gradients along which life-form change takes place as it creates varied climates and thus
promotes diversification of plant species (Lomolino, 2001). Therefore, in recent years
altitudinal gradient has become rapidly popular for investigating patterns in species
richness for management and conservation of biodiversity (Rahbek, 1995; Vetaas and
Grytnes, 2002). Mountains are steep climate gradients where species richness changes
over relatively short distances due to various specific climatic parameters and by
limitation of resources (Lomolino, 2001; Theurillat et al., 2003). Therefore,
understanding changes in plant species richness along altitudinal gradients is imperative
in the study of global climate change (Körner, 2000; Vats and Singh, 2002).
It has been reviewed by Rahbek (1995) that half of the studies revealed a hump-
shaped pattern with maximum species richness at mid elevation. Monotonic decline in
species richness from low to high elevation has also been supported by many workers
(Austrheim, 2002; Kala and Rawat, 2004). But, there are certain cases where both
monotonic decline and hump-shaped relationships have been described (Grytnes, 2003).
In spite of many studies, so far, no common pattern of species richness in relation to
altitude is clear.
Rawal and Pangtey (1994) attempted to assign an altitudinal sequence for the
existing forest zones and types within a range of 1600-3100 m in Sarju catchment of
Kumaun and recognized three forest zones, viz. low altitude (1600-2000 m), mid altitude
(2000-2500 m) and high altitude (2500-3100 m). The altitudinal sequence of forest
vegetation exhibited a sharp compositional change at the mid-altitude zone (2000-2500
34
m) and was considered as an ecotone. A less sharp transition (ecotone) was also apparent
between 2700 and 2850 m, separating the stunted and open canopy growth of sub-alpine
forest in the upper limits.
Uniyal and Prakash (1999) studied the structure of the forest vegetation along an
altitudinal gradient (2550-3600 m) in the Valley of Flowers National Park (3200-6727 m)
and in 2 sites in its vicinity (Ghangaria at 3000 m and Bhyundar at 2600 m) in the Upper
Bhyundar valley of Chamoli district and identified three major vegetation types, viz.
Himalayan moist upper temperate forest (HMUTF; 2550-3000 m), sub-alpine fir forest
(SFF; 3000-3250 m) and sub-alpine birch forest (SBF; 3300-3600 m) based on
importance value. They found average tree density in increasing pattern with the altitude,
while the average basal area decreased with altitude. The low tree density (338 trees/ha)
and high basal area (49.76 m2/ha) in SFF were attributed to high biotic interference and
dominance of coniferous species. The indices of tree species diversity and richness
decreased with increasing altitude.
Species diversity was also observed in decreasing order with increasing elevation
in protected and unprotected sites according to Kiss et al. (2004) who reported the value
of Sahnnon Wiener Index in between 2.77 in unprotected and 2.93 in protected plant
communities distributed at 3300 - 3700 m elevation in alpine meadows of western
Himalaya.
Kharkwal et al. (2005) assessed plant species richness in relation to the altitudinal
gradient between 200 and 5800 m elevation in the Indian central Himalaya (Kumaun) and
reported a total of 2487 species, of which 276 were trees, 355 shrubs, 112 climbers and
1744 herbs. The total number of species including all growth forms was found to be
maximum near low altitude to mid altitude due to overlapping of climatic conditions but
with further increase in altitude it decreased consistently, which is attributed to the
decrease in atmospheric temperature with the increase in altitude and thus concluded that
distribution and species richness pattern in central Himalaya largely depend on the
altitude and climatic variables.
Negi and Gadgil (2002) found that association and distribution depend upon the
preference of the species and reported a strong correlation of woody plants (shrubs and
trees) and moss species richness in temperate mixed oak and coniferous forests through
sub-alpine to the alpine grasslands in Chamoli district of Uttarakhand. They stratified the
35
landscape into five microhabitat types mainly based on the predominant vegetation cover
along the elevation gradient and reported that average rate of species turnover was the
highest in woody plants (1.34 ± 0.17) where elevation was the strongest environmental
predictor of species turnover in all groups of organisms.
Klimes (2003) studied different life forms and clonality of vascular plants along
an altitudinal gradient ranging between 4180- 6000m asl in Eastern Ladakh, which is
quite similar to Lahaul Spiti region for its ecological features and vegetation composition.
Among 404 recorded species, relative abundance of geophytes and chamaephytes
between 4150-5800 m elevation was found to be constant whereas proportion of clonal
plants gradually declined down to zero at highest elevations.
During the assessment of biological richness in different altitudinal zones in the
Himalayan region of Arunachal Pradesh, Roy and Behera (2005) also found that overall
species richness, number of economically important species, medicinal and endemic
species decrease with altitude, where biological richness showed a hump shaped pattern.
Collective effect of aspect of the slope in relation to elevation governing
distribution of species has also been measured in Indian Himalaya region. Studies on the
Quercus forest suggested the dominance of Q. leucotrichophora and Quercus-
Rhododendron species along a southwest facing altitudinal gradient in a montane forest
of Garhwal (Bhandari et al., 2000) where dissimilarity in terms of species richness
between upper and lower slopes was found due to variation in altitude. Further they
found decreasing diversity indices from seedling to tree strata, reflecting poor
regeneration potential of these forest types in central Himalaya.
In coniferous forests of Chakrata region dominated by Cedrus deodara on north-
east aspect, Cedrus deodara - Quercus leucotrichophora - Pinus wallichiana on northern
aspect and Quercus leucotrichophora - Cedrus deodara - Pinus wallichiana on north-
western, Pande et al. (2002) found increasing tree diversity with altitude. Rawat (2001)
studied the various phytosociological attributes of woody vegetation along an altitudinal
gradient and found maximum number of tree, sapling and seedling of various species in
upper slopes and minimum number on lower slopes.
Pande et al. (2001) divided moist temperate forest of Kedarnath forest division of
Garhwal Himalaya into 8 sub-sites as per the aspect and altitude and found that plant
36
species diversity in the whole area was invariably higher for herbs than of the shrubs and
trees where it increases with decreasing altitude. While studying the woody vegetation
along an altitudinal gradient from 1700 to 2100 m above msl in Garhwal Himalaya,
Rawat (2005) reported maximum total tree density (density of tree, sapling and seedling)
for the upper slopes followed by middle and then lower slopes.
Besides dominant tree species, distribution pattern of various medicinal plants
have also been given by various workers. In a study, Samant and Pal (2003) reported
maximum diversity of medicinal plant species below 1800 m elevation and found gradual
decrease in species diversity with the increasing altitude in Uttarakhand.
Kala and Rawat (2004) studied the floral diversity and species richness in the
Valley of Flowers National Park and reported that diversity and richness of plant species
decrease with the increase in altitude from sub alpine to higher alpine zone. Frequency
and density of Nardostachys jatamansi have been reported for a significant positive
relationship with altitude and west facing slopes (Airi et al., 2000).
Several efforts to study the ecological and biodiversity status in Himachal Pradesh
have also been reported. Badola and Pal (2003) analysed 133 rare, sensitive and
threatened medicinal plant species in Himachal Pradesh for their status with the help of
use pattern and their nativity. Importance of vast genetic resource of lesser known
economic plants distributed in trans-Himalayan region covering Lahaul-Spiti district of
Himachal Pradesh have also been described by Chowdhery and Rao (2000) whereas
Singh et al. (2004) reported the agro biodiversity of cold desert in Lahaul valley.
Highlighting the adverse climatic conditions and geographical factors in cold
deserts of Lahaul-Spiti, Husain and Garg (2002) found the comfortable growth of thorny
herbs only, however, seasonal flowering species like Pedicularis bicornuta
(Scrophulariaceae) were also observed in abundance under the shade of Salix plantation.
In a study, Singh and Dogra (1996) reported the distribution of three species namely
Hippophae salicifolia, H. tibetana and H. rhamnoides which grow vigorously in Bhaga
valley having a high regenerative potential even in dry infertile soil and play an important
role in soil erosion control.
Due to tough terrain and poor accessibility in many parts of Himachal Pradesh
like cold deserts, satellite data is also in use to assess the overall distribution of vegetation
cover. By using remote sensing techniques, Joshi et al. (2001) represented the forest
37
cover of Himachal Pradesh. Mapping of Hippophae rhamnoides in the adjoining areas of
Kaza (Spiti valley) has been given using fine resolution satellite data by Roy et al. (2001)
who observed 0.915 km2 area dominated by H. rhamnoides. Besides this, Porwal et al.
(2003) stratified and mapped the distribution of Ephedra gerardiana in Poh region of
Spiti cold desert in Lahaul-Spiti district by using RS and GIS facilities.
For various mountainous regions of the world, a number of workers have given
various theories regarding the distribution of plant species. Variation in plant species
richness of different life forms along an elevation gradient in east Nepal was studied by
Bhattarai and Veetas (2003) who reported that woody life forms had a significant
relationships with climate. The lowest species richness at the both ends of the elevation
gradient showed a hump-shaped pattern of species richness of flowering plants in relation
to altitude. The widest elevation ranges of species at mid-elevations and narrow at both
ends of the elevation gradient have also been reported from Nepal (Bhattarai and Vetaas,
2006).
Similarly, Grytnes and Vetaas (2002) found that number of species in 100 m
altitudinal bands increases steeply with altitude until 1,500 m above msl. Between 1,500
to 2500 m, little change in the number of species was observed, but above this altitude a
decrease was evident in plant species richness along the altitudinal gradient in Nepal. In
Hubei province of China, Yu and Saprunoff (2005) recorded a hump-shaped structure,
with high species richness at middle elevation range.
A peak in the patterns of endemism rates was observed at mid-elevation by Kluge
and Kessler (2006), but when separated for different life forms and microhabitats, some
deviations from the overall pattern emerged. High humidity was observed as a general
predictor for high endemism rates and for the highest species richness. Most importantly,
endemism rates were fairly low on mountain tops that have the smallest available area in
topographically highly fragmented settings.
A decreasing pattern in vascular plant species richness consistently with
increasing elevation in the Alps was also observed by Theurillat et al. (2003) where
distribution was reported to be governed by temperature related processes alongside a
gradual change in physical environment. Moreover, Odland and Birks (1999) reported
that species numbers decline by 40 for every 100 m increase in elevation in the Alps and
Norway. In another study in Norway, species richness peaked at mid altitudes in five
38
altitudinal transects where in two northern transects, species richness decreased with
altitude and further suggested that monotonic pattern of distribution may result from a
decrease in forest species towards the mountain tops (Grytnes, 2003).
Itow and Mueller-Dombois (1992) related the zonation and species distribution
patterns with altitude in Island Santa Cruz, the Galapagos Islands. Floristic and
phytosociological endemism of woody species was found increasing with higher altitude.
In case of herbaceous species, it was low in high altitudes because of their low
endemism. They found that species turnover rate along the altitudinal gradient is three
times higher on the windward south side than on the leeward north side.
In the Gremyachaya valley of Barguzinskii range, eastern Siberia, Valachovic et
al. (2002) studied the changes of vegetation under different climatic conditions and
reported vertical distribution of plant communities. They observed abrupt replacement of
forests by a mosaic of alpine grasslands and shrub communities in the upper zone
communities of mountain tundra, which showed the clearest dependence of forest
vegetation on altitude, although the relation to the moisture gradient and soil conditions
was also very strong. The middle part of this valley was characterized by transition of
non-forest to forest vegetation with various ecotone situations.
Covering a wide range of landscapes, Wang et al. (2003) explained the
distribution of species diversity and life-form spectra of plant communities along an
altitudinal gradient in the mid-section of the northern slopes of Qilianshan mountains.
Species diversity and species richness of both grasslands and forests peaked at the
intermediate portion of the elevation gradient. Furthermore, both life-form richness and
total species richness in a given altitudinal belt also peaked at intermediate elevations.
Among various reasons of declining species diversity along the increasing
elevations, Körner (2000) suggested that due to steep slopes in mountains, the land area
available for biota declines with increasing elevation. Besides this, season length declines
with latitude and altitude. Moreover, there is an analogous situation to the reduction of
land area with increasing latitude. These factors are responsible for declining species
diversity. In addition to these, Fosaa (2004) reported the effect of grazing on the
altitudinal variation in biodiversity while evaluating the biodiversity patterns of vascular
plant species on the basis of species richness at each altitudinal interval in the Faroe
Island, where maximum species turnover was also reported at mid altitudes.
39
Heegaard (2002) focused on the response of species to time of snowmelt and
altitude in alpine areas and observed the changes in species response to snowmelt as
altitude increases and temperature decreases at Finse, Hardangervidda in western
Norway. Of the total 41 taxa analysed, 22 showed a significant change in expected
occurrence in response to time of snowmelt (when a site becomes free of snow) as
altitude increased. He suggested the changes in response due to both environmental
factors (temperature related) and biological interactions where decreasing expected
occurrence of species was probably due to increased environmental severity as altitude
increases.
Soil-plant interactions have also been studied worldwide to understand the effect
of various soil properties on growth and distribution of vegetation in a landscape. Besides
the impact of aspect, altitude and slope, Dhannai et al. (2000) studied the relationship of
soil properties with the characteristics of Quercus leucotrichophora in Garhwal Himalaya
and reported that optimum soil pH, maximum amount of potassium (800 kg/ha) and
phosphorus (36.84 kg/ha) on northeast and southwest aspects supported the growth of Q.
leucotrichophora forests. Higher pH value of soil in the north aspects reflected less acidic
nature resulting into high density of trees and shrubs in a Chir pine forest as compared to
southern aspect in Garhwal Himalaya (Rawat and Pant, 1999).
Analysis of soil collected from a depth of 0-15 cm revealed the highest values of
soil moisture (50.90%), organic carbon (7.10%) and nitrogen (0.50%) on northwestern
aspect at higher elevation of 2800 m (Pande et al., 2001). Distribution of Taxus baccata
reported by Rikhari et al. (2000) in relation to the soil pH revealed its negative
correlation with the presence of Taxus seedlings.
High nitrogen accumulation in forest stands of Picea smithiana and Abies
pindrow has been reported by Gupta et al. (1989) which govern their distribution under
selection system followed by shelterwood and clearfelled systems. Further, a positive and
significant correlation between available and total nitrogen in all the study sites was
observed. Distribution of various forests in relation to soil properties was studied by
Dimri et al. (2006) who reported increase in soil potassium with increasing altitude and
showed highly significant positive correlation with distribution of vegetation. Potassium
accumulation at different altitudes decreased in order of silver fir-spruce (Abies pindrow -
40
Picea smithiana) > ban- moru oak (Quercus leucotrichophora - Q. floribunda) > deodar-
kail pine (Cedrus deodara - Pinus wallichiana) > chir pine (P. roxburghii) forests.
While doing tree layer vegetation analysis in relation to various aspects of soil in
reserve forests of Kumaun, Bisht and Lodhiyal (2005) reported total density of 42.9 -
170.1 individuals per ha for trees, where soil porosity and pH ranged between 52.8 -
64.2% and 5.5 - 6.5 respectively. Airi et al. (2000) found that density of Nardostachys
jatamansi was in positive correlation with organic carbon, moisture content and nitrogen
content of soil.
Vegetation in relation to various physico-chemical properties of soil in different
localities of Lahaul-Spiti was studied by Singh and Gupta (1990) and reported more
alkalinity in silt-clay loam soils where Calcium (Ca), Potassium (K), Sodium (Na) and
Phosphorus (P) were observed in decreasing order affecting the distribution of plants.
They observed absence of substantial leaching of minerals from the soil in most parts of
region that adds minerals continuously in the soil, effecting soil pH which tend to
increase.
In a central Himalayan oak forest of Nepal, Vetaas (1997) found the soil pH as the
most significant indicator of species richness of vascular plants. During 2000, he also
studied the relationships and effect of environmental factors on the forests of Q.
semecarpifolia and reported that canopy disturbance had a negative effect on the number
of seedlings which was related to soil pH (optimum 6), and total nitrogen (optimum 2-
3%), however no clear relationship between the number of saplings and the soil variables
was recorded (Vetaas, 2000). A strong relationship of herbaceous species with the soil
variables suggested rapid changes over a short spatial extent both for herbaceous species
and for the soil variables (Vetaas and Chaudhary, 1998).
Gaur et al. (2003) reported that snowline in Himalaya is rising ceaselessly due to
regional and global climatic change and upward rising of snowline leads to the formation
of moraines with extreme environmental conditions where existing vegetation of such
moraines is scanty, rigorous and possesses different ecological adaptation. Anaphalis
triplinervis was observed to have highest importance value in such areas.
Effect of change in climate has also been studied in distribution patterns of
Himalayan pine (Pinus wallichiana) on north and south slopes by Dubey et al. (2003) to
find its upper elevational limit and estimated that rate of upward shift of saplings was
41
higher on south in comparison to north facing slopes, which mainly was governed by
higher solar insulation favoring growth on relatively warmer south facing slopes.
Nautiyal et al. (2004) also studied the effect of changing climate on vegetation
composition of alpine pasture at Tungnath, Garhwal Himalaya and indicated the
migration of species towards upper slopes of alpine regions.
The effect of latitude on species diversity in different landscapes has also been
reported by various workers. Crow (1993) studied plant diversity on a latitudinal basis
and also revealed a higher level of diversity at warm temperate latitudes. Partel (2002)
described local-scale relationships between plant species richness and soil pH in relation
to latitude and found that the relationship between richness and pH was positive at high
latitudes and negative at low latitudes.
Availability of micro-habitats and habitat specificity of medicinal plants have
been observed an important reason for their localized distribution in concentrated patches
in various habitats like marshy and moist areas, moist rocks, boulder, undulating
meadows, river beds, steep slopes etc. (Kalakoti et al., 1986; Airi et al., 2000; Kala,
2000, 2005c, 2006; Srivastava et al., 2000; Badola and Pal, 2002, 2003; Dhar, 2002;
Dhar et al., 2002; Husain and Garg, 2002; Manjkhola and Dhar, 2002; Uniyal et al.,
2002; Awasthi et al., 2003; Chauhan, 2003; Klimes, 2003, Samant and Pal, 2003; Dhyani
and Kala, 2005; Ghimire et al., 2005; Bhatt et al., 2006; Bisht et al., 2006; Haleema et
al., 2006 and Uniyal et al., 2006a) in Himalayan region.
Bhatt et al. (2005) focused on assessment of quantum of Dactylorhiza hatagirea
(D. Don) Soo in its natural habitats and observed the localized distribution of species that
was not uniform. Kala and Mathur (2002) studied the vegetation distribution in eight
landscape types distinguished along an altitudinal gradient in the trans-Himalayan region
of Ladakh, Jammu and Kashmir, where the highest species diversity was recorded in
stable landscape types followed by undulating areas and river beds. They found most of
the plant species restricted to one landscape type.
In alpine zones of Chhota Bhangal area of Himachal Pradesh, Uniyal et al.
(2006a) provided the information on highly traded and locally used medicinal plants and
reported steep slopes with the highest species richness and diversity. Maximum similarity
in terms of species distribution was observed between steep slopes and undulating
meadows. In high altitude cold desert of Indian trans-Himalaya, Kala (2006) found that
42
distribution pattern of medicinal plants was generally localized because most (27%) were
restricted to marshy and moist areas followed by dry scrub (13%), rocks (12%), boulder
(10%) and undulating land or alpine meadows (9%).
3.4 Phytosociological studies
A number of ecologists have given phytosociological traits of various species in
different ecosystems (Upreti et al., 1985; Bankoti et al., 1992; Agni et al., 2000; Negi
and Gadgil, 2002; Kala and Rawat, 2004) of central Himalaya. In a quantitative analysis
of vegetation along the elevation ranging between 2000-4000 m in Kumaum Himalaya,
Kalakoti et al. (1986) reported 2597 to 18012 cm2/100m2 tree basal cover from different
forest sites. It was observed that tree layer composition differed markedly among the
forests and the vegetation on grassland site was reported more species rich.
Behera et al. (2002) compared the structure of coniferous forests and recorded
subtropical forests less complex in terms of the ecological structure and composition
point of view in comparison to the temperate/ sub-alpine coniferous forests. The total
number of species, genera and families observed for temperate/ sub-alpine coniferous
forests was found to be higher than that for subtropical pine forest. As per Agni et al.
(2000) total tree density varied from 4.3 trees/100 m2 to 11.2 trees/100 m2 and the tree
diversity from 0 to 2.18 in the Tarai-Bhabhar belt of Kumaun central Himalaya located
between 29o25' to 29o40' N and 78o45' to 79o5' E longitude. Absence of young
regeneration of all the important dominant species showed the inability of these forests to
produce progenies due to repeated burning and severe biotic pressure, by both wild and
domestic animals.
In the natural stands of Taxus baccata, Rikhari et al. (1998) found that canopy
volume of the species increased with the increasing circumference at breast height while
studying the stand structure and regeneration in relation to the disturbance levels and
crown cover. The quantitative estimates of regeneration revealed better potential of the
species to regenerate in the moist and shady micro-sites at undisturbed locations.
Among various coniferous tree species, Adhikari et al. (1996) reported density-
diameter distribution curves for Cedrus deodara and Cupressus torulosa. It was
curvilinear for Cypress (C. torulosa), whereas bell-shaped in case of Cedar (C. deodara)
which showed lower representation of smaller and larger trees for Cedar forest and poor
43
conversion of saplings into trees for Cypress forest. Besides this, Rikhari and Adhikari
(1998) have also reported the density-diameter (d-d) curves, diameter class distribution of
dominant species and protective value of temperate forests between 2000 and 3300 m in
Pinder catchment of the central Himalaya where curves for burans (Rhododendron
arboreum), kharsu oak (Quercus semecarpifolia) and alder (Alnus nepalensis) mixed
patch and silver fir (Abies pindrow), maple (Acer cappadocicum) and birch (Betula utilis)
forests were slightly convex, bell shaped, curvilinear, straight line and linear,
respectively. Further it was reported that development of seedlings into trees was not
satisfactory for A. pindrow.
In Kumaun region, Saxena and Singh (1982) described the quantitative profile of
forest structures and reported that all forests indicated a total of four strata; two upper
represented by trees, third stratum by shrubs, and the fourth of herbs. The tree height of
top most stratum decreased with the increase in altitude and crown were more deep than
wide in all forests. Further, the cooler aspects developed a greater canopy index as
compared to the warmer aspects. They found more stable trees on the warmer aspects,
while the cooler aspects showed lower tree stability.
In a phytosociological analysis of forest communities distributed along an
altitudinal gradient (1190-2610 m) in Kumaun Himalaya, dominated by Pinus roxburghii
(chir pine), Quercus leucotrichophora (banj oak) and Q. semecarpefolia (kharsu oak) at
altitudes of 1190-1600 m, 1800-2200 m and 2400-2610 m, Rikhari et al. (1991) reported
total basal area and species diversity across the forest types between 23.1 to 60.7 m2/ha
and 0.22 to 2.76, respectively. Along an altitudinal gradient of 2000-3300 m in the Pindar
catchment, Rikhari et al. (1997) identified 8 forest types on the basis of the importance
value of the dominant species and reported total basal area and biomass for trees in the
range of 10.5-81.5 m2/ha and 49.3-630.7 t/ha, respectively. Tree species diversity and
beta diversity across the forest types were higher for the tree layer as compared to the
shrub layer.
A mountain flank of Jakhni in Tehri Garhwal studied by Bhandari et al. (1998)
revealed total basal area among the forest stands between 23.05 to 63.00 m2ha-1 and the
total density between 660 and 880 plants ha-1. Community diversity was the highest
(2.52) in the middle of the gradient. Dominance of concentration, in general, followed the
44
opposite trend to diversity. Further they reported low value of beta-diversity which
indicated that species composition does not differ significantly across the stands.
Growing stock under various diameter classes in five distinct natural forests of
Cedrus deodara in Garhwal Himalaya were estimated by Bhatt et al. (2002) and reported
the highest total growing stock value (761.70 ±58.73 m3/ha) and total basal area (60.542
± 4.6362 m2/ha) among all the diameter classes at the highest altitude of 2300 m whereas
the lowest values of growing stock (298.54 ± 99.65 m3/ha) and total basal area (34.2763
± 9.9157 m2/ha) were recorded at the lowest altitude of 1900 m.
Effect of various aspects was analyzed by Pathak et al. (1993) while studying the
phytosociological attributes of woody vegetation in 12 stands at South, West, North and
South-East aspects and in 3 positions (hill base, slope and top) in an altitudinal range of
2100-2700 m in Almora. They recorded total tree basal area between 3898-5733
cm2/100m2.
Phytosociological studies of moist temperate forest of Quercus leucotrichophora
in Garhwal Himalaya on North-East, North-West, South-East and South-West aspects
with varying altitudes, highlighted the highest total basal cover (1727.19 cm2/100m2) on
the North-East facing slope (Dhannai et al., 2000).
Nautiyal and Bhatt (1999) presented data on niche width/ location, species
diversity, beta-diversity, equitability, P×F (presence × frequency) index and CI
(continuum index) for important herbs and graminoids in 5 sample stands in an alpine
grazing land in Panwali Kantha region of Garhwal Himalaya at different aspects (SW, SE
and E.) and altitude between 3400-3600 m. Among the graminoids, they reported
Phleum alpinum with maximum niche width, and Bupleurum lanceolatum and
Taraxacum officinale showed maximum niche location. Higher beta-diversity and
equitability values indicated rapid change in species composition and community
heterogeneity according to species adaptability and growth requirements.
Effect of various aspects mainly Northeast, Northwest, Southeast and Southwest
in district Pauri Garhwal was studied by Mishra et al. (2000) to evaluate the growth
behaviour of Sal (Shorea robusta) individuals which reflected regular and random
distribution patterns. The highest total basal cover value of Sal was recorded on the NE
facing slope (5009.04 cm2/100m2), and the highest concentration of dominance (CD)
45
value (dominance index, 0.4321) on the SW facing slope, where species diversity was
minimum. On the other hand, the lowest CD value (0.3115) was observed on the SE
aspect where there was maximum diversity of species.
Khera et al. (2001) reported comparatively higher number of trees and shrubs on
the western aspect. Total tree basal area was recorded from 4.5 m2/ha at hill base to 11.9
m2/ ha at hilltop on the eastern aspect and from 9.3 m2/ ha at hilltop to 16.8 m2/ ha at hill
base on the western aspect. They found lower density of sapling and seedling on western
aspect because of higher anthropogenic disturbances which lead the removal of seedlings
of most of the tree species. Diversity of shrub and herb was higher on both the aspects as
compared to tree diversity because opening of canopy provides greater opportunity for
the recruitment of shrubs and herbs. Further it was concluded that forest was regenerating
because of the presence of few individuals of important species in older girth classes and
higher numbers in younger girths.
Bhandari (2003) reported the composition, population structure and diversity of
blue pine (Pinus wallichiana) forest stands of Garhwal Himalaya with reference to
altitude and aspect. Berberis aristata, Cotoneaster affinis, Pyracantha crenulata and
Pyrus pashia were found the dominant shrub species. Tree layers had a similarity of
43.30 to 82.92%. The higher degree of dissimilarity between the lower gradients of
opposite aspects indicated a significant change in the community structure due to
variation in aspect. Species diversity (H/) ranged from 0.73 to 1.60, 1.71 to 2.53, 1.83 to
2.47 and 1.87 to 2.33 for tree, sapling, seedling and shrub layers, respectively.
Structure of a temperate mixed coniferous forest in the area of Lata was studied
by Kumar et al. (1997) in relation to geo-ecological environment. They found that Pinus
wallichiana constitutes 41% of the total basal area, followed by Cedrus deodara (35%),
Cupressus torulosa (12%), Taxus baccata (9%) and Betula utilis (only 3% on upper
inaccessible terrain) in the tree layer. Total tree density ranges from 33 to 366 trees ha-1,
whereas total basal area was recorded between 1.75 and 24.52 m2 ha-1. Soil of the forest
was reported to be loam (predominantly sandy), with high average levels of organic
carbon (1.2%), low phosphorus (11.28 kg ha-1) and high potash (322.17 kg ha-1) contents.
46
3.5 Traditional knowledge on phytotherapy
India has a rich heritage of having a number of indigenous systems of medicines
such as Ayurveda, Sidha, Unani and Amchi (Nadkarni, 1908; Kirtikar and Basu, 1916;
Shah, 1977). Several ethnic communities including over 400 tribal groups across the
country use more than 7000 species of plants from their surrounding ecosystems to cure
various ailments and diseases (Jain, 1991). The folk knowledge linked with modern
biomedical researches has facilitated discovery of a number of plant based medicines
(Fransworth and Soejarto, 1991). In recent past, a number of ethnobotanists have
published information on folk knowledge associated with plants used in the indigenous
health care systems from different parts of the country.
Exploring the hidden treasures of traditional knowledge in Rajasthan, Tripathi
(1999) reported a wide range of medicinally important plant species used by the villagers
and tribal communities, whereas around 243 genera belonging to 76 families have also
been reported by Jain et al. (2005) which are used by the tribes of about 50 villages
around the Sitamata Wildlife Sanctuary of Chittorgarh and Udaipur districts as means of
primary health care to cure various ailments. They revealed new ethnobotanical uses of
24 plant species belonging to 20 genera. In a floristic survey, a total 61 ethnomedicinal
plants belonging to 38 families were recorded by Katewa et al. (2004) used traditionally
by tribal communities inhabited in the Aravalli hills of Mewar region. In case of birth
control and to cure various sexual diseases by the tribals in southern Rajasthan, Jain et al.
(2004) reported 53 species belonging to 33 families through interviews with local
medicine men and women, birth attendants and other knowledgeable persons to check
birth control, including abortion at initial stages, preventing conception or by making
either member of the couple sterile and to cure problems of leucorrhoea, gonorrhoea,
menorrhagia, to regularize menses and syphilis in both the sexes.
A total 27 plant species used in the treatment of genito-urinary diseases by the
Kandhas of Orissa have been reported by Behera and Misra (2005). In Madhya Pradesh,
Samvatsar and Diwanji (2000) reported the use of 13 plants for the treatment of jaundice
among tribal communities.
Traditional knowledge among the Korku tribe in the Chikhaldara, Achalpur and
parts of Morshi in Amravati district of Maharashtra was compiled by Jagtap et al. (2006)
and reported the traditional uses of 66 plant species belonging to 40 families. The
47
documented ethnomedicinal plants were mostly used to cure skin disorders, diarrhea,
jaundice, tuberculosis, migraine, menstrual problems, fertility problems, urinary
problems, piles, wounds and poison bites.
Traditional phytotherapical use of 54 plant species belonging to 26 families has
been described by Ayyanar and Ignacimuthu (2005) among the Kani tribals in Kouthalai
of Tirunelveli hills of Tamil Nadu to cure skin diseases, poison bites, wounds and
rheumatism.
Bhandary et al. (1995) reported 98 medicinal preparations from 69 plant species,
used by the Siddis of Uttara Kannada in the state of Karnataka and found 40 hitherto
unknown medicinal uses of known medicinal plants. Information on the use of stem sap
of Calamus thwaitesii as an antifertility drug, and the use of the flowers of Ichnocarpus
frutescens and rhizomes of Hedychium coronarium in the treatment of diabetes were
novel information. About 52 herbal preparations from 31 plants belonging to 21 families
as herbal remedies to cure skin diseases from the same area have also been reported by
Harsha et al. (2003). In other studies, Hebbar et al. (2004) revealed that 35 plants
belonging to 26 families are being used to treat different types of oral ailments like
toothache, plaque and caries, pyorrhea and aphthae in Dharwad district. 18 plant species
belonging to 13 families and 18 genera used as traditional herbal remedies for
gynecological disorders in women of Bidar district of Karnataka have been documented
by Vidyasagar and Prashantkumar (2007).
While highlighting the traditional utilization of medicinal plants of North-Eastern
states, Jamir (1997) reported 14 major tribes of Nagaland for their traditional use of
native plants as medicines. He found that Panax pseudo-ginseng was used as tonic and to
dissolve tumours, Viscum articulata for rheumatism, Clerodendrum colebrookianum for
reducing high blood pressure, Bambusa tulda for abortion, Laggera alata for stomach
ulcer and tumor. Traditional phytotherapy practiced among different ethnic communities
of Mizoram have been documented by Lalramnghinglova and Jha (1997) whereas Kala
(2005b) also investigated the wealth of medicinal plants used by the Apatani tribe of
Arunachal Pradesh and documented the medico-ethnobotany of 158 medicinal plants.
In different areas of Uttar Pradesh, Singh et al. (2002) collected the information
on folk medicinal uses of 125 plants which are used against cough, cold, dysentery,
diarrhoea, ulcers, diabetes, male and female weakness, snake-bite and skin disorders. To
48
cure gastro-intestinal problems in Sonbhadra district, Narain et al. (2007) documented
ethnobotanical remedies of 19 species in traditional practices.
Previous literature on ethnomedical knowledge, particularly from the western
Himalayan region include Shah and Joshi (1971), Uniyal and Chauhan (1973),
Maheshwari et al. (1980), Gupta et al. (1980, 1981), Srivastava et al. (1981), Nautiyal
(1981), Gaur et al. (1983), Maheshwari and Singh (1984), Dar et al. (1984), Brij Lal and
Dube (1984), Purohit et al. (1985), Sundriyal et al. (1987), Singh (1988), Shah and Jain
(1988), Kaul (1994), Upreti and Negi (1996), Samant et al. (1996), Maikhuri et al.
(1998b) and many others.
Mamgain and Rao (1990) presented a list of 41 medicinal plants with their
medicinal uses and mode of application of Pauri Garhwal Himalaya. About 25 plants
used for medicinal purposes within Nanda Devi Biosphere Reserve have been reported by
Samant et al. (1994). After these efforts, Kaul (1994) brought to light many plants with
dual properties, i.e. as supplementary food and also as folk remedies. Information on
ethnomedicinal and ethnonutritional properties of 7 native Himalayan herbs, Allium
victoralis, Caralluma tuberculata, Dioscorea pentaphylla, Dipsacus inermis, Phytolacca
acinosa, Polygonum alpinum and Pueraria tuberosa were described in detail.
Gaur and Bhatt (1994) discussed the folk utilization of ferns by the inhabitants of
Deoprayag tehsil in Garhwal Himalaya and reported 41fern species with their traditional
uses. Ethnobotanical information of Jaunsari tribe of Chakrata (Rana, 1997) and
Dehradun (Singh, 1997) has also been discussed in detail. Dobriyal et al. (1997) reported
29 plant species used in folk medicine of which 11 species were used for disorders
related to digestive system, 6 species for skin infections and 3 for joint or muscular pain.
Chantia (2003) also studied ethnomedicines of Jaunsar-Bawar area. Bhatt and Negi
(2006) evaluated 66 plant species belonging to 52 genera and 41 families by the tribal
people of Jaunsar and reported 17 species for their new medicinal uses from the region.
Kala et al. (2004) reported a total 300 plant species used in curing 114 ailments
prevailing in various ethnic and non-ethnic communities of Uttarakhand and reported
Vitex negundo as the most important species used for the treatment of more than 48
ailments.
Samal et al. (2004) covered 19 settlements between 800-2000 m and consulted as
many as 500 respondents to document more than 50 indigenous healthcare practices in
49
central Himalaya. Traditional information among 60 traditional ‘Vaidyas’ in Uttarakhand
regarding the types of ailments treated with plants and the preparation of herbal medical
formulations was compiled by Kala (2005a) and reported 243 herbal medical
formulations prepared by ‘Vaidyas’ for the treatment of 73 different ailments. A total of
138 species (35 species of trees, 22 shrubs and 81 herbs) belonging to 98 genera for the
treatment of liver diseases have been reported by Samant and Pant (2006). Recently
Garbyal et al. (2007) in their ethnomedicinal survey documented various traditional
phytomedicines used by Bhotias of Dharchula sub-division in Kumaun.
Herbal remedies from Jammu and Kashmir have been documented by Koul
(1990), Kumar and Naqshi (1990), Kaul et al. (1989), Khan et al. (2004) and others.
Besides these, Ballabh and Chaurasia (2007) in their significant contribution reported that
health care of tribal population in Leh-Ladakh region is mainly dependent on traditional
system of medicine which is popularly known as Amchi system of medicine. To cure
cold, cough and fever, they identified and documented 56 valuable plant species
belonging to 21 families with all the relevant information among Boto (the Buddhists)
tribal community of Leh-Ladakh.
Considerable information on traditional knowledge has been compiled by various
ethnobotanists in Himachal Pradesh. Kapur (1993) documented a total 136 plant species
of medicinal importance used by Kangiris and local physicians in Kangra valley.
Similarly, Sharma (1999) conducted ethnobotanical studies on ‘Gaddis’, a tribal
community in district Kangra of Himachal Pradesh and reported 67 plants species of
ethnobotanical importance.
Tribal communities of Chhota Bhangal were explored ethnobotanically by Uniyal
et al. (2006b) compiling the importance of medicinal plants in traditional healthcare
practices. They found 35 plant species commonly used by local people for curing various
diseases where medicinal uses of Ranunculus hirtellus and Anemone rupicola reported
from the area were new to the ethnobotany of western Himalaya. Similarly, preparation
of ‘sik’, a traditional recipe served as a nutritious diet to pregnant women in the area was
new and has not been documented elsewhere.
In Kullu district, Singh (1999) highlighted 109 plant species belonging to 41
families and 86 genera from the Chhakinal watershed for their traditional importance, of
which 73 species were used to cure variety of diseases by the local people. In Banjar
50
taluka of Kullu district, Natarajan et al. (2000) recorded ethnobotanical uses of 34 plant
species by the local women. Similarly, Uniyal (2003) also focused on the indigenous
knowledge of women in utilization of a total 25 medicinal plants for curing various
diseases from three villages of Tirthan valley. In Parbati valley, Jain and Puri (1994)
gathered the information on 37 local plant species used for medicinal purpose. However,
Sharma et al. (2004) also reported medicinal importance of 50 plant species belonging to
45 genera and 28 families used by the inhabitants of the same area. Sharma and Brij Lal
(2005) recorded indigenous therapeutic application of 9 plants in Kullu valley. While
studying the ‘Malanis’, a tribal community in Kullu district and other inhabitants of
Parvati valley, Sharma et al. (2005) have also reported first hand information on 35 plant
species used in traditional phytotherapy.
A considerable amount of information on traditional medicines of plant resources
of Lahaul-Spiti reported by earlier workers (Koelz, 1979; Aswal and Mehrotra, 1987;
Kapahi, 1990; Kala and Manjrekar, 1999; Brij Lal et al., 2001, 2004; Sood et al., 2001;
Srivastava and Chandrasekar, 2004; Chandrasekar and Srivastava, 2005; Singh and
Chauhan, 2005; Sharma et al., 2006 and Kanwar et al., 2007) is also available.
Gurmet (2004) described ‘Sowa-Rigpa’, commonly known as Tibetan or Amchi
medicine, among the oldest surviving well-documented medical traditions of the world
which has been popularly practiced throughout central Asian Himalayan region including
Ladakh and entire Lahaul-Spiti in Himachal Pradesh.
Kapahi (1990) collected 50 folk-lore claims from local inhabitants of Lahaul
valley. Kala and Manjrekar (1999) studied the ethno-medicinal uses of 62 plant species
occurring in Spiti sub-division. An account on the traditional use of Hippophae
rhamnoides was compiled by Brij Lal et al. (2001). Chaurasia et al. (2001) reported
traditional use of 39 plant species. Indigenous therapeutic uses of Dactylorhiza hatagirea
to cure general weakness, cough, bone fracture, spermatorrhoea, stomachache and wound
healing has also been reported by Brij Lal et al. (2004).
Srivastava and Chandrasekar (2004) described ethno medicinal applications of 10
plant species used by the tribals of Pin Valley National Park in treating dysentery, however
Chandrasekar and Srivastava (2005) also provided the information on traditional uses of
plants with the dosages and combination with other plants in curing jaundice by the local
community residing in and around Pin Valley National Park. A total 26 plant species in
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traditional phytotherapy practiced by the inhabitants of Spiti valley have been reported by
Sharma et al. (2006).
In Lahaul valley, Singh and Chauhan (2005) documented traditional practices of
herbal medicines in different villages and reported 43 plant species, belonging to 25
families in traditional use. Recently, Kanwar et al. (2007) described some traditional
fermented foods consumed by people of Lahaul-Spiti area.
Based on ethnobotanical studies, Valsaraj et al. (1997) selected 78 plants used in
the treatment of infectious diseases among the Indian traditional medicines for
antimicrobial screening. For antibacterial activity, Samy et al. (1998) selected 34 plant
species belonging to 18 different families on the basis of folklore medicinal reports
practiced by the tribal people of Western Ghats. Aqueous residues of 16 different
ethnomedicinal plants have also been studied for this purpose by Samy et al. (1999).
Similarly, Samy and Ignacimuthu (2000) screened 30 Indian folklore medicinal
plants for antibacterial properties. Based on the information of various Indian traditional
systems of medicines, Grover et al. (2002) reviewed 45 plants that have been mentioned
for anti-diabetic activity. Chhetr et al. (2005) have also found 37 species of plants used as
antidiabetic agents. Recently, Gautam et al. (2007) highlighted that of 17,500 higher
plant species occurring in India, only about 365 species have been evaluated so far for
antimycobacterial activity and described 255 (70% of 365) plant species from a wide
range of families that have shown antimycobacterial activity. They also screened certain
plants for antimycobacterial activity and highlighted the promising plant species for
further investigation as leads for drug development.
3.6 Conservation implications
Several biodiversity conservation programmes have been started in the country
based on the findings and recommendations of various workers. Zobel and Singh (1997)
discussed various approaches to solve the problem of insufficient data regarding the
status of forest vegetation and suggested the collection of basic ecological data
throughout the Himalayan region for the effective conservation of bioresource.
In a different study on the conservation of valuable plants in south India,
Srinivasamurthy et al. (2003) described the important Medicinal Plants Conservation
Areas (MPCA) for in-situ conservation involving local people in conservation efforts.
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They reported under this programme about 45% of flowering and medicinal plants
diversity in gene banks in Karnataka, Kerala, Tamil Nadu, Andhra Pradesh and
Maharashtra. They further suggested that germplasm conserved in the MPCA network
can be used to provide authenticated quality planting material for commercial cultivation
to meet rising demands of the herbal industry and to reduce the pressure of over-
exploitation on natural populations of these plants.
Kala (2000) recorded the lack of any kind of studies on the ecological and
population characteristics of plant species in many regions of Indian Himalaya including
Lahaul-Spiti, and, therefore, Uniyal et al. (2002) stressed that these studies are required
for designing conservation plans and to develop appropriate strategies for long term
monitoring of plant species. Highlighting the status of medicinal plants, Dhyani and Kala
(2005) observed that majority of current research programmes on medicinal plant
conservation have been focused on species level instead of ecosystem one. Although,
there are many protected areas (PAs) across the Himalayan region but not a single PA is
basically known for conservation of medicinal plants.
Shrestha and Dhillion (2003) suggested sustainable harvesting methods and
domestication of potential commercial species which require attention in the local forest
operational plans due to haphazard harvesting and over-exploitation. Singh (2004)
suggested the appropriate changes required in the marketing pattern, extraction procedure
of medicinal plants, improvement in traditional knowledge, empowerment of local
communities and innovative government policies and programmes. He stressed that in
management plans, government-owned forestland and other uncultivated lands should be
used to grow medicinal plants as constituents of natural vegetation.
Dhar et al. (2000) believed that excessive anthropogenic activities if controlled
can check the declining population and availability of medicinal plants in the Himalayan
region. They suggested an urgent need for identification and notification of areas for
conservation of medicinal plants on a priority basis. An approach for prioritizing
strategies for action was proposed by Dhar (2002) which is based on three important
attributes viz. geographical range, ecological amplitude and anthropogenic pressure.
Besides, the approach highlights the importance of involving indigenous communities,
traditional institutions, and NGOs to complement efforts of academics, scientists, and
government departments to ensure conservation and utilization of plant bioresource.
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Joshi and Rawat (1997) suggested ex-situ and in-situ cultivation of valuable and
threatened species of alpine and sub-alpine areas of Northwest Himalaya by establishing
high altitude nurseries in their natural habitat, so that regular supply to pharmaceutical
industries and users could be maintained and germplasm will also be conserved. In Nanda
Devi Biosphere Reserve (NDBR), cultivation of medicinal plants has become a major
activity with conservation-oriented land use changes. Maikhuri et al. (1998a) described
the agronomic practices and uses of eight medicinal and aromatic plants cultivated in the
NDBR buffer zone villages of Garhwal Himalaya. These conservation efforts have not
only the potential for economic betterment of people but also help bioresource
conservation of biosphere reserve.
Srivastava et al. (2000) identified certain areas within the Northwestern
Himalayan range extending from Jammu and Kashmir to western borders of Nepal,
which can be declared reserves to protect the germplasm and declining population of
medicinal plants particularly threatened species. Besides notification of the areas for
protection, Pascal et al. (1996) is of the opinion that preparation of database of rare and
threatened taxa is of immense importance based on intensive surveys.
For the conservation of rare and endangered medicinal plants of Spiti cold desert
of Himachal Pradesh, Kala (2000) proposed protection of habitats of commercially viable
taxa. He suggested that areas rich in these species should be given special care and
priority in management plans. He proposed the establishment of Medicinal Plant
Conservation Areas (MPCA) for the conservation and production of selected economic
and indigenous species that may be grown commercially for the benefit of local
communities.
With reference to the conservation programmes of Arnebia benthamii, a high
value Himalayan medicinal plant, Manjkhola and Dhar (2002) suggested establishment of
herbal gardens in the vicinity of its natural population, which will not only reduce
pressure on the natural population, but will also generate a new source of rural economy.
Based on the status and extraction patterns of Jurinea dolomiaea in alpine meadows of
Kumaun Himalaya, Awasthi et al. (2003) suggested its large scale cultivation in suitable
habitats. Cultivation of valuable herbs is one of the important alternate to reduce the
pressure on their wild populations. Therefore, these efforts have already been started for
species such as Carum carvi and Allium stracheyi in Nanda Devi Biosphere Reserve
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(Maikhuri et al., 1998a). Bisht et al. (2006) supported the need for conservation
initiatives for Himalayan medicinal plants in general and Angelica glauca in particular.
They suggested that utilization pattern, traditional knowledge base and trade of medicinal
plants show trends that are not ideal for sustainability in the Indian Himalaya and
suggested ways to overcome the problem.
To conserve the rare and precious medicinal plants of cold arid zones of Himachal
Pradesh, Singh and Chaurasia (2000) suggested establishment of nature reserves and
botanical gardens along with the development of package of practices to popularize their
commercial cultivation. Community based ex-situ cultivation of such plants was
emphasized to reduce in-situ harvesting pressure by Badola and Pal (2002). Guan et al.
(2000) highlighted that adverse impact of tourism and environmental pollution on plant
species diversity can’t be ignored which is needed to be checked to control habitat
degradation of natural populations of various plant species. Similarly, Samant et al.
(2007) reported developmental activities, particularly the construction of hydroelectric
projects which are also causing a great loss of biodiversity in the Indian Himalayan
region.
Taking into account rapid degradation and loss of natural habitats, Shankar and
Ved (2003) suggested in situ conservation of wild population by establishing taluka-level
herbal gardens. Chandola (2005) reported that wild populations of Gentiana kurroo has
been rediscovered after a lapse of 50 years and suggested serious Species Recovery
Programmes to be initiated for the highly threatened plants to relocate their distribution and
habitat specificity.
While highlighting the importance of collaborative efforts, Biswas (1988)
suggested the establishment of conservation plots in representative forest types, landslide
control measures, the setting up of high-altitude botanic gardens, tissue culture studies,
inclusion of species in the Red Data Book, and education of the public for the
conservation of flora. People's participation is needed to be strengthened for productive
outcomes in conservation programmes (Negi, 2000) and therefore incentives are also
required to promote meaningful participation in biodiversity conservation (Badola and
Hussain, 2003).
Besides conserving the plant bioresource, the traditional knowledge regarding the
use of plant species as medicine is also vanishing rapidly due to several reasons.
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Traditional health-care system, which used to be the lifeline of the people of remote,
high-altitude areas, is on the verge of extinction. The wealth of information, which is
preserved as an unwritten materia medica of the tribal folk is slowly fading, and oral
tradition of passing on knowledge from generation to generation is also decreasing.
Therefore, several studies suggest rapid documentation of this valuable information
before it is lost forever. Ethnic groups inhabiting north-west and trans-Himalayan region
have been living in isolation for thousands of years and their knowledge of indigenous
uses of native plants needs to be studied before it gets extinct (Kaul et al., 1990).
Therefore, Dhar et al. (2002) suggested collaborative work plan involving all the
functional groups to preserve the traditional knowledge system and practices, for the
conservation of plants and upliftment of the rural economy of hilly region.