general introduction - shodhgangashodhganga.inflibnet.ac.in/bitstream/10603/18675/7/07_general...
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GENERAL INTRODUCTION
Introduction
The Himalaya is a vast mountain system covering partly or fully eight
South Asian countries viz. Afghanistan, Bangladesh, Bhutan China, India,
Mynmar, Nepal and Pakistan. The small kingdom of Nepal with an east
west extent of 900 km covers a significant area of the Himalayan mountain
system and is located between the river gorges of the Indus and Yarlung
Tsangpo/Brahmaputra. From climatological point of view the Nepal
Himalaya represents a transition between the warm-wet climate of Eastern
Himalaya (including Arunachal Pradesh, Assam, Bhutan, West Bengal, and
Sikkim) and the drier Western Himalaya (including Uttar Pradesh, Himachal
Pradesh, Jammu and Kashmir) (lves, 1988). The linkage between
upstream deforestation and downstream flooding is a key trans
national/regional consideration because 'upstream causes' of deforestation
are often located in one country and 'downstream effects' in another
(Thompson and Warburton, 1988). Thapa and Weber (1990) made a
watershed management study for the Upper Pokhara Valley to look after
the environmental degradation issues coming out of the natural resource
competition for the subsistence livelihood. In the context of 'Himalayan
Environmental Degradation' theory Metz (1989, 1991) analyzed the
Nepalese Himalayan farmers' dependence over forest and their knowledge
linkage with forest management system. Virgo and Subba (1994)
compared the land use change between 1978 and 1990 in Dhankuta
district of east Himalaya, Nepal. Jackson et a/., 1998; Schweik eta/., 1997
studied the land cover land use change and forest institutions in the
mountain region of Nepal. Ecological development perspective of Arun
Basin has been attempted in the work of Shrestha (1989).
Traditional agroecosystems
The Himalayan environment influences not only the people living in
this region but also many more living in the adjoining plains. Water and
sediment flow from the Himalaya determine productivity in the Indo
Gangetic plains that supports one of the most thickly populated and most
productive regions of South Asia (Nathan, 1989, lves and Massereli, 1989).
Agriculture, considered in terms of aggregate area, constitutes a minor land
use, but is extremely important, as it remains the primary occupation of
ninety percent of people of the region. Agricultural land in the Himalaya is
in the form of patches in the matrix of forests. Crop-livestock mixed
farming, practiced in these lands in the Himalaya is sustained with fodder
and manure inputs derived from the adjoining natural forests and
meadows. Access to modern technologies is severely constrained by the
poor economic status of the local inhabitants as well as poor infrastructure.
Availability of adequate inputs from natural ecosystems had been a key
feature of sustainability of this traditional agriculture needs to be considered
as inter-dependent and complementary objectives rather than independent
sectors. Increase in1
population pressure together with penetration of
markets and tourism led to many undesirable trends: the erosion of crop
2
diversity, depletion of soil fertility and environmental functions of natural
ecosystems (Ramakrishnan, 1992; Rao and Saxena, 1994; Hurni, 1999;
Joshi et a/.,; Maikhuri et a/., 1999). The common cultivation of maize and
potato was associated with increased reclamation of dry agricultural land,
particularly from forest, and so contributed to the advanced state of
deforestation existing by the late eighteenth century in Nepal (Regmi,
1978). Bajracharya (1983) traced the linkage between the food, fodder and
fuelwood of a mountain community of eastern Himalaya, Nepal.
Mountain societies are dependent upon traditional complex multi
species agroecosystems organized in space and time (Ramakrishnan,
1992; Swift et a/., 1996). Though highly energy efficient, with little or no
energy subsidies from outside (contrast with modern agriculture receiving
inorganic fertilizers and other chemical inputs), economic productivity is low
(Altieri, 1983; Maikhuri and Ramakrishnan, 1990,1991; Maikhuri, 1996;
Semwal and Maikhuri, 1996). However, with high biodiversity within, these
agroecosystems offer a great potential of coping with environmental
uncertainties, (Ramakrishnan, 2001).
Land holdings are small and fragmented, total average land area per
household in a study done in 1 0 villages was 1.63 and persons per hectare
of agricultural land was 4.0 in a mid hill area of central Nepal (Mahat et a/.,
1987). Average farm holding size was 0.89 ha, split into a larger plot (0.68)
of terraced slopes and a smaller, levelled land plot (0.16 ha) in the valley in
a study conducted in western Himalaya, India (Singh eta/., 1997). Human
3
density ha - 1 cultivated land in Jaidvepur, Dalimsain and Hathnur village in
a traditional village agroecosystem in Garhwal Himalaya, India was 5.11,
7.00 and 7.77 respectively. Likewise, livestock density ha - 1 cultivated land
was 5.90, 6.57 and 5.48 in the above villages respectively (Semwal and
Maikhuri, 1996).
Farmyard manure was observed to be the main energy input in the
settled upland farming. It contributed about 58, 66 and 72% of the total
energy in Jaidevpur, Dalimsan and Hathnur respectively (Semwal and
Maikhuri, 1996). In contrary, labour was the major energy input in all
traditional shifting agricultural (Garo, Khasi, Mikirs, 20, 10, 5 years)
systems, whatever be the length of cultivation cycle as reported by
Maikhuri and Ramakrishnan (1990).
Energy and monetary inputs into the shifting cultivation practiced by
the Nishis in Arunachal Pradesh (north-east India) declined with shortening
of the cultivation cycle. The decline was most pronounced for labour. Slash
and burn was the most labour-intensive of all operations and this input
increased under shifting cultivation cycles. Under valley cultivation, labour
was the major input followed by organic manure (Maikhuri and
Ramakrishnan, 1991 ). The energy output/input ratio ranged between 18.1
and 55.2 with minimal values under Khasis in 5 year shifting cultivation
cycle in tribal communities of Meghalaya in north-eastern India (Maikhuri &
Ramakrishnan, 1990). Energy and monetary efficiencies of the shifting
cultivation varied depending upon the cycle length, with maximum
4
efficiency (outpuU input ratio = 43) under a 10 year cycle and minimum
(outpuUinput ratio = 24) under a 60 year cycle (Maikhuri and
Ramakrishnan, 1991).
In traditional framing systems above 4000 masl, in Latin American
region where maca (Lepidium myenil) is the only crop capable of offering
farmers secure yields. Research shows that maca grown in virgin soils or
those fallowed between 5 - 8 years, exhibited significantly higher yields
(11.8 and 14.8 tonnes/ha, respectively) than maca grown after bitter
potatoes (11.3 tonnes/ha) (Altieri, 2000).
Double cropping as expected, showed higher inputs in terms of
human and bullock labor and seed quantity compared to single cropping.
The output is also higher in the double-cropping pattern. Singh and Singh,
(1992) have reported the output per unit of input from central Himalayan
agroecosystems to range from 5.5 to 14.46 for single cropping and from 3.8
to 6.0 for double-cropping.
Maize-potato dominated system enabled a yearly household income
of US$ 899 compared to US$ 1771 cardamom dominated system in Sikkim
Himalaya (Sharma et a/, 2000).
Forest ecosystems
High species richness of forests of eastern Nepal has been
documented in a number of studies over the past 150 years, from Hooker's
(1845) initial explorations to more recent work, including the pioneering
5
studies of Schweinfurth (1957, 1984), Hara (1966), Stainton (1972),
Dobremz and Shakya (1975), Numata (1980), Oshawa (1983), Shrestha
(1989), and Miche (1989). Stainton (1972) in 'Forests of Nepal' described
the variation of the temperate forests with those of other physiographic
regions. Numata (1980) explained the vertical zonation and dynamics of
vegetation of the humid Himalays in eastern Nepal. Biodiversity Profile
Project (1995) document gives an account of the biodiversity of Mid
hills/High-hills/High Himal physiographic zones and forest ecosystems of
Eastern/ Central/Western Mid-hills of Nepal. Ali (1977) explained the Arun
valley of east Nepal as 'ornithologist's paradise' based on the species
richness and diversity. Fleming et a/., (1984) and lnskipp and lnskipp
(1989) reported 440 bird species from the eastern Himalaya, Nepal, with
majority of them breeding in that area. Carpenter and Zomer (1996)
reported a high local species richness throughout low-to-middle elevation
forests (below 3,500 m). Extensive stands of late successional, closed
canopy forests occur throughout the Makalu-Barun Conservation Area,
especially above 2,000 m. At lower elevations, spatially limited but
ecologically significant stands are found within locally protected raniban
forests and in corridors of near-tropical riparian forest within the deepest
river valleys that penetrate a considerable distance in the project area.
The establishment of Rhododendron arboreum and Quercus
semecarpifolia are considered to be less competitive and able to coexist
with a whole range of species (Oshawa eta/., 1986). The higher seedling
survival of late successional species in shade as compared with the open
6
and reverse behaviour of early successional species are related to their,
adaptation to different light regimes 1n the forest community
(Ramakrishnan, et at., 1982). If such periods of opportunity were repeatedly
available at different times and locations within the landscape, long lived
species could persist and remain dominant and this seems an important
condition for high diversity in the forest (Loucks, 1970; Tarman and Likens,
1979). In a forest ecosystem, if disturbance is small, suitable microclimate
conditions may remain prevalent on different pockets, which may lead to
germination and establishment of large number of species (Sundriyal and
Sharma, 1996).
Decrease in increasing size of tree diameter class often reflects
healthy growth of forest (Sundriyal and Sharma; Carpenter and Zomer,
1996). Thick litter accumulation often reduces seed germination of canopy
species (Janzen, 1970; Singh and Singh, 1992).
Forests in the Himalaya are under pressure, through both internal
and external forces, with· adverse impacts on the fuelwood, fodder and
other daily needs of the forest dwellers, and also on forest based
government revenues (Eckholm, 1982; Singh et at., 1984; Ramakrishnan et
at., 1992). Increasing flow of outside population in the form of tourists has
further aggravated the pressure on forests (lves and Pitt, 1988; Thapa and
Weber, 1990). Studies have shown that deforestation in Himalaya has
implications for agriculture not only in the adjoining hills and mountains, but
also in the plains far below (Pandey and Singh, 1984; Mahat, eta!., 1986;
Blackie, 1988; Virgo and Subba, 1994; Maikhuri, eta/., 1997).
Agriculture in the Himalaya and elsewhere is closely linked with the
forest ecosystems. Traditional agroecosystems are sustained through the
energy-flow from the adjoining forest ecosystems. Since, agriculture in the
traditional societies is highly dependent upon the natural resource base,
farmyard manure and human labour, quality of the forest from where they
extract the natural resource becomes important (Tsegye, 1997; Datta and
Virgo, 1998; Ellis-Jones, 1999; Sen et a/., 2000). Studies have shown that
agroecosystems located in natural resource rich areas are generally more
energy efficient than those located in resource poor areas of the mountains
(Maikhuri, 1992, 1996; Semwal and Maikhuri, 1996) ..
Earthworms
Earthworms play an important role in litter decomposition and
maintenance of soil fertility (Syers and Springett, 1984). Most of earthworm
species sampled from temperate regions belong to the family Lumbricidae
(Edwards 1983). In contrary, species from diverse families like Almidae,
Kynolidae, Megascolidae, Endritidae and Ocnerodrillidae have been
sampled from tropical ecosystems (Dash and Patra, 1977; Krishnamoorthy,
1985). The role of earthworms in nutrient cycling was found significant in
shifting agriculture in north-east India (Bhaduria and Ramakrishnan, 1989,
1991) as also reported for temperate agroecosystems (Edwards & Lofty,
1982) and forest systems (Satchell, 1983). The quantity, quality and timing
8
of leaf litter inputs to the soil system are very important in determining
earthworm abundance and distribution (Nemeth, 1981; Nemeth and
Herrera, 1982; Fragoso and Lavelle, 1995). An increase in earthworm
activity with pine stand age which reached a maximum in the sacred grove
could be related, to increased litter fall and more favourable soil moisture
retention, because of higher humus content in the latter situation (Bhaduria
and Ramakrishnan, 1991).
Variation in earthworm density and biomass in relation to changes in
land use-land cover have been discussed elsewhere also (Bhaduria et at.,
1997, 2000) The rainy season peak in earthworm population size and
activity is more common and is due to favourable soil moisture,
temperature and humidity (Edwards, 1982; Bhaduria and Ramakrishnan,
1991).
Common ecological theory predicts that biodiversity in a given group
and a given location should be greater in tropics than in temperate regions.
This, however, is not the case of earthworms. At the local scale, the
number of species of a given community was rather similar between
temperate forests, Mediterranean pastures and tropical savannas.
Similarly, average number of species in tropical rain forests was not
significantly different from temperate deciduous forests (Fragoso and
Lavelle, 1992). Species richness is usually higher in natural forests than in
agroecosystems and pastures (Fragoso et at., 1997).
9
Studies in Mexican humid tropics Fragoso (1993); Fragoso eta/., (1993,
1995); Fragoso and Rojas, (1994) showed that majorities of the native
species were restricted to natural forests or riparian habitats of the exotic
species to disturbed ecosystems.
Bhaduria and Ramakrishnan (1991) found three spec1es to be
endemic out of a total of five observed in natural forest in north-east India.
After slash and burn (Bhaduria and Ramakrishnan, (1989) the community
lost two native species and was invaded by one exotic species. Invasion in
the successional communities is relatively easy than invasion into the
climax phase of the biome (Ramakrishnan, 1991).
Earthworms greatly increase soil fertility, and at least part of this
must be due to the increased amounts of mineralized nitrogen that they
make available for plant growth (Edwards, 1972). Earthworms consume
large amount of plant organic matter that contains considerable quantities
of nitrogen and much of this is returned through excretion (Edwards, 1972).
Cultivation has adverse effect on earthworm population. This could be due
to mechanical damage due to cultivation, to the loss of insulating layer of
vegetation or to a decreased supply of food as the organic matter content
gradually decreases (Edwards & Lofty, 1972).
Meeting livelihood needs
Forest resources in the Upper Pokhara valley are used for extraction
of fuelwood, fodder, timber and raw materials for cottage industries. One
10
quarter of the total fuelwood and one third of the fodder requirement of an
average household was fulfilled by trees grown in forms and by crop
residues, the rest being met from forests (Thapa and Weber, 1990). In the
buffer zone of Makalu Barun Conservation Area, Nepal farmers extract
certain proportion of their fodder requirement from the wild trees planted in
their field terraces (Carpenter and Womer, 1996). Pandey and Singh
( 1984) estimate that forests meet 71% to 87% fodder requirements of the
local community.
The mean annual fuel wood consumption in Pangma village, mid
Himalaya, east Nepal was 4290 kg. per household, 35% of it derived from
cutting down the trees and 65% from lopping and/or gathering branches
and dead wood (Bajracharya, 1983). The estimated mean value of 408 kg
"air dry" fuel person -1 year -1 agrees quite closely with estimate of 458 and
471 kg person - 1 year - 1, of which as little as 40 percent might be derived
from wood, in Sindhupalchok, mid Hill, central Nepal (Mahat et a/, 1987).
Fox (1983) reported fuelwood consumption rate of 537 kg person -1 year -1
in Bhogateni Panchayat in mid-hillwest Nepal. Per household consumption
of fuel wood, fodder in Mamlay watershed, Sikkim Himalaya was 4000-
5800 kg, 5700 kg per year respectively. Likewise, timber volume required
for household repairs, furniture was 2.5 - 4.2 m3 over a time interval of 15-
20 years and 5 - 7 m3 for new house construction over a time interval of 20
- 30 years (Sundriyal and Sharma, 1996).
II
Wildlife
The Eastern Himalaya supports a wide diversity of wildlife
(especially birds) resulting from complex physiography and bioclimatic
zonation (lves and Messerli, 1989) and also because of their location at the
convergence of the Palearctic and Oriental Zoogeographical Realms
(lnskipp, 1989). Despite of a relatively small geographical area, Nepal is
regarded as one of the richest natural animal reserves in the world. About
1 0 percent of the known birds in the world have been sighted in Nepal
(Majupuria, 1998). Shrestha (1989) has reported a high degree of biological
diversity (mostly plant species and birds) in Arun valley; the site studies
here lies within this valley. Ali (1977, 1997) considers Arun valley, as the
natural boundary of the winter migrating birds descending from the higher
elevation, and a region where avifauna from the rest of the Nepal and the
western Himalayas becomes sensibly discerntble. Chhetri et a/. (2001)
reported a rich diversity of birds in Kanchenjunga region of Sikkim
Himalaya, which share the natural boundary with Nepal Himalaya, too.
Fleming eta/., (1984, 2000), lnskipp and lnskipp (1985) have made an
extensive report on the bird diversity of Nepal have found the east region to
be the richest pocket of avifauna.
Wildlife study in Nepal dates back to nineteenth century (Hodgson,
1831), through the studies on the mammals of Nepal and Sikkim Himalaya.
Oliver ( 1984) studied the distribution and status of Hispid Hare and Pygmy
Hog, likewise Oli, (1991) studied the stereotyped behaviour of snow
12
leopard and Barking Deer in Nepal Himalayas, in recent years. Majupuria
( 1984) and Yon jon ( 1990, 1991) also contributed on the wildlife study of
Nepal Himalayas. The Biodiversity Profile Project (1995) provided an
overview of the whole Nepal's mammalian fauna. This document includes
an account of wildlife abundance according to physiographic regions.
Shrestha (1994) published on the Wildlife species occurring in the
Himalayan region. Shrestha (1995) has enumerated the fishes of Nepal.
Chalise (1999) reported the behavioural and ecological aspects of the
Macaca assamensis from Makalu-Barun area, east-Nepal.
The avifauna of Nepal is very diverse (Ali and Ripley, 1987; Fleming
et a/., 1984; lnskipp and lnskipp, 1985). There are some 850 species,
about 82 per cent of which breed locally. Arun valley is known as
ornithologist's paradise, with well excess of 440 species. The Arun valley
shows a change in the east-west distribution of avifauna and mammals,
although the delineation of species is not sharply marked. However, there
are twenty species whose range is markedly confined to the east.
Some 22 percent of the breeding birds of Nepal are judged to be at
risk. While most are represented in protected areas (lnskipp, 1989), habitat
is being rapidly degraded due. to agriculture and grazing. Most heavily
affected are those species that require forests, especially obligate dwellers
of less disturbed dense forest. High proportion (36 percent) of Nepal's
breeding species are altitudnal migrants, which spend much of their time
outside the nesting season at lower elevations. About 68 percent of
13
wintering spec1es and 10 per cent of those for which Nepal may hold
internationally- significant breeding populations..- utilize forests and shrubs.
A total of some 436 breeding birds have been recorded from the eastern
forests of Nepal.
In a study in northern Spain, afforestation on former arable land
showed no difference in species richness of bird species in forest bird
communities. In breeding ground also no significant difference observed.
However, species richness was positively correlated with· prevalence of
undergrowth shrubs and with plant species richness (Diaz eta/., 1998).
Only sixteen percent or 86 of the forest species are adapted to
breed in habitats heavily modified by man, such as groves, gardens, scrub
and the edge of cultivation. One bird that has benefited from such change
is the 'Spiny Babbler', which was "rediscovered" after being assumed to be
extinct. However, some twenty bird species recorded in Nepal are now
probably extinct (lnskipp, 1989). lnskipp (1989) reported that an estimated
168 breeding birds in Nepal occur within the Temperate Zone, but only ten
per cent have their home range restricted to this ecological zone. About 25
per cent of the total species of Nepal are likely to have viable population
sizes. Sub-alpine and upper temperate forests (at elevations of 2400 to
2800 meters in the east) are internationally important for breeding birds, as
they support high numbers of species.
A corridor of disturbance related to contemporary indigenous and
tourist use (tree harvesting, burning, grazing) was observed along the main
14
trail of upper Barun Valley in Makalu-Barun National Park and
Conservation Area, and impacts appeared to be growing in frequency and
magnitude (Byers, 1996). Koirala and Rai (1999) reported the decrease of
avifauna in Tamar River Basin due to the increased development activities
including tourism. Habitat degradation has resulted in the movement of
wildlife towards the croplands of the farmers adjoining to the forested area
causing crop depredation in Kanchenjung Conservation Area. However,
local opinion about wildlife was divided, while some people think it is 'bad'
to kill these animals, others demand for elimination or reduction in
population of animals as well as highly dangerous encounters threatening
life and livelihood. (Muller-Boker and Kollmair, 2000).
Bird diversity was higher at the open canopy condition because
opening of canopy is likely to accompany an increase in habitat diversity
(Block, 1989; Daniels, 1989). Human pressure has altered species
composition and canopy organization which may result in avifauna species
richness and abundance (Chhetri et a/., 2001). Bird species richness as
well as diversity were higher in open canopy habitats, compared to close
canopy habitats at lower altitude, but were not at higher altitudes (Chhetri
et a/., 2001). Edge effect plays an important role in determining species
richness (Kilgo eta/., 1997).
Fleming and Giualiano (1998) did not find any difference in species
richness of border-edge cut and uncut plots, possibly because the study
plots were undoubtedly smaller than the species home ranges and
15
probably that the plots were used by individuals, inhabiting surrounding
forests (Aigner et a/., 1998), or size of patches (open forest area) formed
were small enough to bring about variation in bird species diversity (Kilgo et
a/., 1998).
Significant agricultural damage due to wildlife is reported from
developed as well as developing countries (Murton and Wright, 1968;
National Academy of Sciences, 1970; Stone eta/., 1972; Guarino, 1975;
Jewell et a/., 1981; Caldecott 1988). Problem wildlife includes Songbirds,
Deer, Wild pig and other large mammals. In Srilanka, for example,
Elephants cause much damage near national parks and are the focus of a
special World Bank report (Seidenstisher, 1984).
Crop damage by wildlife has become a pertinent issue these days
along the immediate periphery of parks and reserves. These issues are
attracting significant economic and political consideration of the Park
management (Mishra, 1982; Uprety, 1985). Upreti (1985) noted that
buckwheat and barley were reportedly destroyed by Wild Pigs, Langurs,
and Macaque Monkeys in Langtang and Lake Rara National Parks;
Himalayan Black Bear and Tahr destroying crops in Sagarmatha National
Park in Nepal. However, quantitative information on crop losses is very
little. For example, crop yield were attributed to wildlife in Royal Chitwan
National Park was exceeding fifty percent. Croplands lying near to forests
are depredated by Deer, Bears, Porcupines, Goral, Tahr and Monkeys in
and around Makalu-Barun Conservation Area causing a loss of 20 to 25
16
per cent of the production (Banskota and Upadhyay, 1989). It has
contributed to the food deficit in those areas (Humphrey, 1980; Banskota
and Upadhyay, 1989). In a similar study in Nanda Oevi Biosphere Reserve
in Garl:lwal Himalaya, India crop damage in low altitude villages near core
zone was three times higher to the high-altitude villages away from the core
zone (Maikhuri, eta/., 2000). In Nepal, crop damage is very common along
the immediate periphery of parks and reserves in the T erai (Milton and
Binney, 1980; Mishra, 1982, and Upreti, 1985). Complete losses were
noted in a few villages located in the highest crop damage zones along the
edge of the park. Problem species consisted of Rhinoceros, Chital (axis
deer), Wild pigs, Monkeys and Parakeets. There are reports that while
defending their fields from marauding rhinos people were killed. The main
crop depredators in the Terai and Hill zones of Nepal appear to be Bears,
Deer, Wild Boars, Monkeys and a variety of Birds. Some persons have
reported that as much as third of their crops were consumed, but (Jackson,
1990) raises doubts on accuracy of such estimates. Habitat degradation
has resulted in the movement of wildlife towards croplands bordering
forested area. Agricultural fields present some wildlife at the right time of
year with abundance of food. It is not hard to see why animals are attracted
to areas with grain or other crops. Ripening maize is richer in protein and
carbohydrates as well as some mineral nutrients than most of the natural
plants available in adjacent forests or shrublands. Unlike forest plant
species, many of which grow in isolated stands or scattered throughout the
forest, agricultural crops occur in relatively large, concentrated stands.
17
Thus, animals feeding upon such items do not have to expand as much
energy searching instead they can satisfy their hunger quickly and
efficiently provided they are not killed by angry farmers in the process
(Jackson, 1990). Crops are only available for a short time each year in the
mountains, but this period may coincide with the time that many species
are "fattening-up" in preparation for winter, or when females are nursing
and therefore have significantly greater energy demands.
Towards the end of summer, bears have only a month or two before
they hibernate. The females give birth in a winter den. Their newborn
young are very small, thus requiring large amounts of milk, which must be
provided for the first month or so of life. Furthermore, it is conceivable that
survival rates of cubs during their first few months of life are improved if the
mother has access to crops in late summer and early fall (Jackson, 1990).
Not all individuals of a particular species raid agricultural fields. Only
those animals with home ranges that encompass croplands can do so.
Since most adult mammals have strong attachments to their "home area",
they are not likely to visit sites outside their normal zone of use or to shift
their home ranges in response to ripening fields or quickly changing
cultivation patters. Subadults or juveniles, by contrast, can become
significant pests after they are forced from maternal ranges by their parents
or dominant conspecifics. As they disperse in search of a home range of
their own and encounter already-occupied sites, there may be increased
pressure for them to settle around habitations. Also, juveniles are less
18
experienced in locating or catching food, and may thus take those items,
which are most abundant, and readily available, irrespective "of risk
involved. Crop losses are probably most substantial in the upper
subtropical and lower temperate ecological zones (1500 to 2500 meters),
along the edge between continuous forest and dense human habitation,
zones that fall almost entirely within the proposed Community Managed
Resource Area (CMRA) (Jackson, 1990).
Most of the pest animals are species which are associated with
successional or "disturbed habitats". They are thus benefited by human
actions that promote secondary forest succession, i.e., selective thinning
and opening up of dense forest by tree cutting, livestock grazing or burning.
Thus, slash-and-burn activity may actually enhance habitat conditions for
bears or barking deer, by creating grassy open glades within the forest, by
increasing the availability of some foods (including maize and other grain
crops), or simply by encouraging successional shrubland that provides
more browse or fruit shrubs and trees. The carrying capacity of old-growth
forests is usually much lower than that of successional forests, because of
a paucity of fruit or protein-rich undergrowth foliage. Any increase in the
amount of edge between forest, shrubland, grassland and agricultural field
improves foraging opportunities for generalized species like Bear, Langur
or Rhesus and Barking deer.
Milton and Binney (1980) reported that not only the crop losses
happen to be greatest along the edge of protected areas, but loss rates
19
have increased over time. Villagers of Chitwan experienced crop losses of
75 per cent in 1978, whereas, losses were three times less a decade
earlier, before the park was established. Given enforced regulations
against hunting and other park-induced measures, populations of some
wildlife species should increase markedly over time. As surplus individuals
migrate from saturated, protected sites within or near the core area, human
communities along the peripheries of parks are likely experience increased
crop depredation.
Population increases cannot be sustained indefinitely, and crop
losses are not likely to be uniform, or even inevitable. The most severe
impacts will occur in areas known as "hotspots", or sites that provide ideal
habitat conditions for pest wildlife species. Management is essential to
minimize the development of "hotspots" within areas dedicated to
community development, to replace grain crops with cash crops
unattractive to wildlife, or to compensate owners for their crop losses under
specified circumstances.
The idea birds can be used to monitor the environment is not new.
Folklore and natural history observation suggests that some aspects of bird
behaviour can be used to predict changes in the weather. Aristotle, in his
Historia Animalium of 342 BC,. describes how the behaviour of Cranes
( Grus grus) shows the weather to come: they will fly to a great distance and
high up in the air, to command an extensive view; if they see clouds and
signal of bad weather they fly down again and remain still (Thompson,
20
1910). According to Inwards (1869), the early arrival of Cranes in autumn
signals that there is going to be a particularly severe winter. The same
prediction is made by early autumn arrival of the fieldfare Turdus pilaris in
its winter range. In a similar vein, early northwards movements of grey Lag
geese (Anser anser) in spring are considered to indicate that a period of
settled spring weather is coming (Swann, 1913; Furnnes, eta/., 1993).
Compared to natural forests within landscapes disturbed by
silviculture, forests within landscapes disturbed by agriculture, irrespective
of the extent of disturbance, had fewer forest-associated species, long-
distance migrants, forest-canopy and forest-understory-nesting species,
and greater numbers of edge-associated species, including avian nest
predators (Rodewald and Yahner, 2001).
In two different studies, abundance of bird pests was found
dependant on vegetation complexity, rather than resource status of the
food. Tendency of birds to feed closer to vegetation appeared to be a
predator avoidance tactic (Nakamara and Mutusoka, 1991; Subramnaya,
1994).
Ecotourism
Tourism in general has emerged as the fastest growing industry
worldwide and is in the forefront of global economic growth (Sharma,
2000). Between 1989 and 1998, international tourism receipts grew by
about 8.1 percent annually. Mountain tourism globally is estimated to
21
account for about 15- 20 percent of the tourist industry (Mountain Agenda,
1999). Tourism is identified as one of the key activities for providing
livelihood opportunities to mountain people in the process of attaining
sustainable mountain development (Agenda 21, UNCED). Mountain
tourism development encompasses activities that attract tourists, provide a
strong stimulus to community development (Banskota and Sharma, 1995,
1998; Boselli, eta/., 1997; Rai and Sundriyal, 1997).
Amqng HKH countries, China is the only country that appears in the
world's top 40 international tourism destinations, ranking 5th worldwide, with
24 million arrivals in 1998. In terms of revenues from international tourism,
both China and India appear in the top 40 list with earnings of US$ 12,500
million and 3159 million respectively (WfO, 1999).
The HKH region, comprising of contiguous mountain terrain of
Afghanistan, Pakistan, India, Nepal, Bhutan, Bangladesh, China and
Myanmar, attracts international tourists in a few cases only. Nepal .
(422,000), Bhutan (5400), Ladakh (12000) and Sikkim (16000) in India, and
Tibet Autonomous Region of China (33,000) in the year 1997 are important
destinations for foreign tourists (Sharma, 2000). However, statistics show
that domestic tourist flow in larger countries like China, India and Pakistan
is quite significant (Paudyal, 1999). Available statistics on the growth rate of
tourism in the above regions/countries show, with a few exceptions, a
steadily increasing trend. In Nepal, the UP Hills, Himachal Pradesh, and
22
the HKH region of China, the average annual growth rate for the last
decade has remained above 10 per cent (Sharma, 2000).
International tourism earnings comprised 3.8 per cent of the GOP of
Nepal and accounted for 18 per cent of total foreign exchange earnings in
1996. In Bhutan, international tourism earnings accounted for 2 per cent of
GOP in 1997. Tourism is the 9th largest foreign exchange earner in
Pakistan. In the UP Hills and Himachal Pradesh in India, tourism accounted
for nearly 20 per cent of state GOP. From the viewpoint of revenue
generation the contribution of tourism has been important and there seems
to be enormous scope for its growth in HKH region (Sharma, 2000).
There is considerable debate over what ecotourism means
(Campbell, 1999). Stewart and Sekartjakrarini (1991) argue that the
multifaceted nature of expanded, principle-based definition leads to
ambiguity in interpretation, a definition which includes community
development is increasingly promoted (Boo, 1990; Kutay, 1992; Ecotourism
Society, 1992; Norris, 1992; Cater, 1994). The notion is associated with the
growth of the nature- related travel sector as Ecotourism Society defines
ecotourism: " responsible travel that conserves natural environment and
sustains the well-being of people (Lindberg and Hawkins, 1993).
The prime aim of eco-tourism is to promote a symbiotic relationship
between tourism and the environment, with a particular focus on benefitting
local economies through a decentralized framework (Ghurmi, 1997;
Sharma eta/., 2001 ). Mou~tain environments offer excellent opportunity for
23
organizing nature-based tourism as aspired by trekkers and mountaineers.
However, these areas have a fragile ecosystem and socio-cultural heritage
with meager tolerance of stress and limited carrying capacity (Poudel,
1998).
Tourism development cannot be viewed in isolation from
conservation and natural resource management and mountain
development, as it is the mountain resources that form the very basis of
mountain tourism as well as the basis of survival of local communities
(Dunsmore, 1988; Banskota and Sharma, 1995, 1998; Sreedhar, 1995).
The lack of realization has not been able to contribute meaningfully to wider
mountain development. The unique mountain environment found in the
Himalayas is therefore becoming increasingly degraded, thereby reducing
the tourist and visual appeal of the areas, and, at the same time, local
communities that lies amidst these rich environmental resources continue
to lead a subsistence life (Banskota and Sharma, 1995). The true economic
value of tourism, when measured in terms of willingness to pay, is likely to
be much higher than the current levels of expenditure by tourists (Wells,
1993).
Annapurna Conservation Area Project (ACAP) is the first protected
area to allow local residents to live within its boundaries and maintain their
traditional rights to access and use of its natural resources. It is also the
first protected area managed by local experts that does not use assistance
of the army to protect the dwindling resource base on which the region
24
depends. Instead, it invests the financial resources that area available for
community development and local capacity building in the region (Ghurmi,
1997).
If critical areas and safe minimum standards were defined without
addressing the needs of the local people, the very purpose of delineating
such areas would be defeated. In ACAP, the formation of such critical area
has taken into consideration local people's need for firewood, fodder, and
other resources. The formation of Conservation and Development
Committees (CDCs) at grass roots' level is the mainstay of ACAP's
community empowerment approach (Banskota and Sharma, 1995). The
effectiveness of the hunting ban in ACAP has been reflected in increased
wildlife around villages, and this has in turn led to livestock depredation. A
compensation mechanism has yet to evolve, and, to a certain degree,
illegal hunting may be related to the lack of compensation. Crop raid by
wildlife is also in rise (Banskota and Sharma, 1995).
A ban on tourism to the core zone of Nanda Devi Biosphere Reserve
m Garhwal Himalaya has eliminated an important source of income for
local people. Added to this, conservation policies have restricted grazing in
the core zone, collection of non-timber forest products (NTFP) and removal
of dead logs from Van Panchayat forests. Damage to livestock, agriculture,
crops, fruits and localllivelihood by wildlife have also affected the villagers.
Villagers have rarely been given an explanation of the curtailment of their
rights, and have rarely been provided with adequate alternatives. The
25
experience of top down conservation programme has caused a break down
in local community-nature relationship and is causing increasing hostility of
local people towards conservation/management of natural resources
(Maikhuri eta/., 2000).
Wunder (2000), in a study conducted to see the linkage between
income incentive and conservation, in Cuyabeno Wildlife Reserve, Ecuador
found that the effectiveness of tourism income depends on the incentive
structure inherent in the mode of participation, and on the substitution
versus complementarity of other productive activities: only if tourism
changes labour and land allocation decisions, it will have a local
conservation impact. This study suggests that the autonomous
communities may operate more efficiently than the salary receiving or
paternalistic ones.
Ownership issue raises the question of how. far local people can be
empowered in the control of their newly created resources, and whether or
not they can transfer the skills and leadership they have developed to
future generations. It is likely that the numbers of trekkers will increase
rapidly once the infrastructure is in place. This may lead to the area being
overrun and overused, and end in a classic case of the "boom and burst".
All of these questions must be addressed seriously if ecotourism to a given
area is to succeed. The future of ecotourism relies heavily on who is
responsible for marketing, setting the trekking quotas, increasing the entry
26
fees once the infrastructure is in place, and the carry1ng capacity of a
tourist destination themselves (Ghrumi, 1997).
In a mountain context, carrying capacity with respect to tourism is an
attempt to define the level of tolerance or compatibility between tourist
activities and demands of the ecological, social, cultural and economic
support systems of the mountains to meet those demands. Therefore, in
ecological terms the level of tourism and tourist activities has to be
compatible with the maintenance and enhancement of the ecological
balance, biological diversity and biological resources. In social and
economic terms, tourism development has to ensure that its benefits are
broadly shared, that it is compatible with the culture and values of the
people, and that it maintains and strengthens community identity and
enhances people's control over their own lives. In economic terms, tourism
development needs to facilitate a process of development that is
economically efficient, relives pressure on fragile resources, and allows and
promotes management of resources in ways that not only support present
needs but which can super the needs and aspirations of future generations
(WCED, 1987).
Carrying capacity of a particular site or area may be seen as a
function of a variety of tourist resources; the nature of "mountain
specificities", particularly the tolerance and fragility of resources to use; the
number and frequency of visitors; their activity types and intensity of
resource uses; provision and maintenance of infrastructural facilities;
27
monitoring and management of resource use sites; and the expectations,
attitudes, and behaviour of visitors as well as resource managers and local
communities (Sharma, 1995).
In the context of carrying capacity, it is convenient to categorize
tourists on the basis of their purpose. National Tourism Statistics (1992)
recognizes six categories in this context i.e., a) holiday and pleasure, b)
business, c) official, and d) convention/conferences e) "trekking and
mountaineering" f) pilgrimage. Out of these, category trekking and
mountaineering fall purely into mountain tourism (Shrestha, 1995).
A mountain ecosystem is generally fragile and vulnerable to rapid
deterioration due to modern exploitative forces such as tourism. Most
mountain societies function in a more or less closed system depending
upon subsistence agriculture and the traditional use of natural resources.
After centuries of interaction with the nature these societies have acquired
equilibrium with the natural environment. The time- tested knowledge of
local people may provide accurate and reliable means for environmental
monitoring. The coming and going of migratory birds, or the appearance
and disappearance of frogs and toads, festival cycles, and the agricultural
calendar all are tied with the agro-climatic dynamism of the environment
(Shrestha, 1995).
Carrying capacity is determined by a number of biotic/abiotic factors
that create environmental resistance or impose limits on the growth of the
population. The capacity of a mountain ecosystem to support healthy
28
population, while maintaining its productivity, adaptability, and capability of
renewal, is drastically affected by the rapid growth of tourism. This force
readily weakens and breaks the closed circuit of the traditional economic
circle of remote mountain societies and links them with the market
economy and more affluent societies. The notion of carrying capacity is not
only the measure of how many individuals (tourists) a particular habitat can
sustain at a given time but also the measure of maximum optimum impact
that a particular habitat can retain (Shrestha, 1995).
Mountain areas, as distinct from other physiographic units, have
certain objective conditions or specificities. These conditions of
inaccessibility, fragility, diversity, 'niche' or comparative advantage, and
marginality add a particularly critical dimension to tourism in the mountains
and call for particular ways of responding to these specificities (Jodha,
1991).
Inaccessibility has traditionally restricted external linkages to
mountain economies. Trekking, mountaineering, and other forms of nature
based adventure tourism are helpful in bringing economic incentives in
these areas. It can also generate employment in transportation and the
creation of infrastructure. For isolated remote area~ with a limited resource
base, tourism may also provide scope for improvements in livelihood that
would not be possible otherwise (Jodha, 1991; Sharma, 1994).
Low-carrying capacities and vulnerability of resources to rapid, and
often irreversible, degradation under conditions of high-intensity use are the
29
fragility characteristics in mountains (Jodha, 1991 ). These adversities are
however, tackled by the ecocentric view of traditional societies widely
reflected in their attitudes towards plants, animals, soils and water
(Ramakrishnan, 2001 ).
Diversity manifests in a range of micro-environmental variations
leading to a variety of ecosystems in the mountains. Mountain tourism can
be used to enhance the linkages with these different production systems
and resource-management regimes (Shrestha, 1989, Jodha, 1991 ).
Diversity also provides opportunities for the harnessing of specific
comparative advantages in the tourism - from rafting down rivers to trekking
and mountaineering at higher altitudes (Sharma, 1994; Gurung and
Coursey, 1994; Thapa and Gurung, 1997; Rai eta/., 1998).
Niche, an outcome of the diversity, is expressed in the form of
relative or absolute comparative advantage by particular locations and
areas for small- scale specialization, and mountains provide specific niches
for tourism activities (Jodha, 1991 ). Mining, logging, hydro-electric
generation and promotion of ·skill-based ethnic- and culture specific
handicrafts are some niche related opportunities that flow from mountain
tourism (Gurung, 1995; Sreedhar, 1995; AI- Jalaly eta/., 1995; Sharma,
2000)
Mountains have historically been neglected in terms of development
priorities and have always been considered marginal entities, economically
and politically (Jodha, 1991 ). With the advent of community forestry
30
management and ecotourism practices a decentralized decision-making
and resource reinvestment approach has come up to benefit mountain
community development (Maharana et at., 2000; Muller- Boker and
Kollmair, 2000; Jodha, 2001 ).
Present study
In the present study of two adjacent villages viz. Tamafok (hereafter
referred as TF) characterized by low intensity degradation and
Madimulkharka (hereafter referred as MM) characterized by a high intensity
degradation in a landscape of Tinjure-Milke region of, eastern Nepal
Himalaya are compared in respect of ecological and economic efficiencies
of agroecosystems and impacts of wildlife and tourism on the local food
production system and livelihood. Both the villages are 1) dependent on
natural resource base 2) practice crop-livestock mixed farming 3) and are
characterized by subsistence economy.
31