Sahyadri Conservation Series: 23 ENVIS Technical Report: 53,  May 2013
http://www.iisc.ernet.in/
Status of Forest in Shimoga District, Karnataka
http://wgbis.ces.iisc.ernet.in/energy/
1Energy and Wetlands Research Group, Centre for Ecological Sciences, Indian Institute of Science, Bangalore – 560012, India.
2Member, Western Ghats Task Force, Government of Karnataka, 3Member, Karnataka Biodiversity Board, Government of Karnataka
*Corresponding author: cestvr@ces.iisc.ernet.in

STATUS OF WILDLIFE

Wild fauna diversity is one of the most gracious gifts of nature to the region.Wildlife has been diminishing at an alarming rate during recent years, particularly during the last 20-25 years as a result of deforestation, fragmentation of animal habitats, etc.Wildlife and wildlife habitat play a vital role in the ecological and biological processes that is essential to life itself. The functioning of the biosphere, and hence the maintenance and enhancement of human life, depends on countless inter actions among plants, animals and micro organisms.These ecological processes are essential for agriculture, forestry, fisheries and other endeavours necessary to human life. They also help maintain environmental quality by degrading and otherwise removing some pollutants and by preventing waste accumulation. Some of the biological processes in which wild species play a key role are pollination, germination seed dispersal, soil generation, nutrient cycling, predation, habitat maintenance, waste break down and pest control. Wildlife habitat regardless of whether it is upland or wetland habitat, is significant because of a number of functions it performs to support wildlife. Wildlife needs adequate space and habitat for the basic life requirements (Sameer Ali et.al 2007).

The primary step taken towards conservation and management measures is to preserve a small proportion of forest and declare it as bioreserve, wildlife sanctuary or national park. The criteria followed in this regard, involved prioritising regions based on naturalness, diversity, rarity and or uniqueness, and size. Such planned actions were aimed at preserving and conserving biodiversity and natural resources of a region/nation or at larger scale contributing to global biodiversity. At the same time, it helps in improving local biodiversity and the environment in and around such areas in a natural and protected environment (Sameer Ali et.al 2007). The areas having significant conservation value are declared as national parks and wildlife sanctuaries under the Wildlife (Protection) Act, 1972, which was amended in 1991. The Act specifies that, the state governments are empowered to declare any area as a sanctuary or a national park as per the procedures, for the purpose of protecting, propagating or developing wildlife or its environment. The National Parks and Wildlife Sanctuaries have been studied for ecological significance and to implement measures to conserve endemic and endangered species of flora and fauna.

There are two wildlife sanctuaries and one bird sanctuary in Shimoga forest circle.

  1. Shettihalli Wildlife Sanctuary
  2. Sharavathi Valley Wildlife Sanctuary
  3. Gudavi Bird Sanctuary

1. SHETTIHALLI WILDLIFE SANCTUARY

Shettihalli wildlife Sanctuary with a spatial extent of 395.6 Sq.km is spread over parts of three taluks of Shimoga district: Shimoga, Hosnagara and Thirthahalli taluks (Figure 1). It is situated between 13° 40' to 14° 5' N and 75° 10' to 75° 35' E (Karnataka forest department, 2006). The vegetation in the region mainly consists of dry deciduous, moist deciduous and semi evergreen types. This Sanctuary was constituted under the government notification No.Afd.47.F.W.L.74 dt 31st October 1974. After declaration of Shettihalli wildlife Sanctuary, protection and development activities towards better management of wildlife had been initiated by wildlife wing of forest department.

The Karnataka Forest Act, 1963 and Rules 1969 regulate working in the forest areas. The State has 5 National Parks and 22 Wildlife Sanctuaries covering an area of 6576.76 sq. kms, which forms nearly 15.17% of the total forest area as protected area(http://karnatakaforest.gov.in). Wildlife (Protection) Act was enacted during 1972 by Government of India to provide for the protection of wild animals, birds and plants and with a view to ensuring the ecological and environmental security of the country.

ANd9GcTJ6NI02K4duGTZAtHA-dIgFcqm1qaLGO_SiatsHuTHgwOZfaApVUpOl6Hmiw North: From Ayanur along the southern portion of Ayanur-Hosnagara road upto Rippenpet running from East to West.
South: From Konandur the boundaries of Riponpet, Hanagere and Thirthahalli range forest area upto Mandagadde running from West to East.
West: From Ripponpet along eastern portion of Ripponpet-Tirthahalli road including Mugudthi state forest upto Konandur which runs north to South.
South-East: From Mandagadde along the western portion of Shimoga running from South to
North-East: Starting from Shimoga, the line runs along the western portion of Bangalore-Honnavar road upto Ayanur (Karnataka forest Department, 2006)
Figure 1: Shettihalli wildlife sanctuary, Shimoga

The overall area of the sanctuary is plain to undulating with a few pockets consisting of very steep and undulating terrains and hillocks. These consist of perennial nalas and a number of small streams. The highest peak is Shankaragudda with an altitude of 1031 meters. The Sanctuary receives rainfall from south west monsoon. The intensity of rainfall is more during June to September with an average rainfall of 2000 mm. The average minimum and maximum temperatures are 12° C and 38º C respectively (Karnataka forest Department, 2006).


Figure 1: Shettihalli Wildlife Sanctuary

History

During early 20th century the forest within Sanctuary were under the control of Previously State of Mysore. For better management of forests and wildlife these forests were declared as ‘protected forests’ during 1905-1920. Table 1 details the spatial extent of forests in Shettihalli Wildlife Sanctuary.

Table 1: Forests in Shettihalli wildlife sanctuary

Name of Forest Extent (in Ha)
Hanagere RF 6755.0
Kudi RF 2730.0
Harohitlu RF 1795.00
Masaruru RF-Block vii 1,2,3,6,7,8,9 1060.0
Kumadhwathi RF 3817.0
Baruve RF- vii 12 to 14 807.0
Mugudthi RF 194.0
Anesara RF 1819.0
Puradal RF 2591.0
Shankar RF 9330.0
Sacrebyle RF 3886.0
Arakere MF 368.0
Anupinakatte MF 497.0
Basavapure MF-XII 1 317.0
Bedankalmatti MF-XII 2,3 693.0
Keegadi MF-XIII 20 144.0
Talale MF-XIV13 242.0
Kullunde MF-XIV14 204.0
Halasavala MF- XIV10 325.0
Kanagalakoppa MF- XIV11 150.0
Mandagadde MF-XIV8 223.0
Bommenahalli XIV15 50.0
Mandagatta MF 942.0
Kittanduru MF VIII23 294.0
Bide MF VIII24 209.0
Muniyur MF VIII 25 332.0
Anupinakatte Pltn 87.0
Sacrebyle Pltn 100.0
TOTAL 39560.00

During 1960-1965 Linganamakki reservoir was constructed in Sharavathi river valley, which led to submersion of many villages. The people affected by this Hydro-Electric project were shifted from protected area and allowed to settle in Shettihalli Wildlife Sanctuary. In this way more settlements of rehabilitated village come into existence in the sanctuary leading to encroachments and clearing of forests. The animals found in this sanctuary are Tiger, Panther, Wild elephant, Bison, Sambar, Spotted Deer, Barking deer, Mouse deer, wild pig, Porcupine, Sloth bear, Wild Cats etc. In Shettihalli Wildlife Sanctuary there are both natural forests and artificial plantations. It consists of 11 reserve forests, 14 minor forests and 3 plantation areas (Karnataka forest Department, 2006). 

Vegetation:

Forest types:

  1. Southern tropical dry deciduous type: This type of forests is seen in Puradal, Anesara, Sacrebyle, Shankargudda, Kudi and part of Hanagere state forest. The top canopy consists of Terminalia tomentosa, Terminalia bellerica, Tectona grandis, Anogeissus latifolia, Lagerstroemia lanceolata etc. The second canopy consists of Wrightia tinctoria, Zizyphus zuzuba, Santalum album, Emblica officinalis, Cassia fistula, Shorea talura, Randia domatorum and bambbos etc. The ground floor consists of grassy patches.
  2. Southern tropical moist deciduous type: This type of forest is seen on the western side of the sanctuary i.e, part of Hanagere state forest, Kumadwathi state forest, Mugudthi state forest etc. Bambusa aurundanasea and Dendrocalamus strictus occur throughout the area.Terminalia tomentosa, Tectona grandis, Lagerstroemea lanceolata, Adina cardifolia, Dalbergia latifolia, Xylia xylocarpa, Grewia tiliafolia are the other species.
  3. Semi evergreen type: This type of forests is seen in parts of Hanagere state forests and Kumadwathi state forests. The importantspecies found areDipterocarpus, Hopea, Terminalia, Hopea, Xylia, Michelia and Bambusa species.

Plantations:The sanctuary has about 6000 Ha of Teak plantations.

Aquatic habitat:The Tunga reservoir bordering the sanctuary has a good population of otter, fish, and some crocodiles, water birds like Cormorants and Snake birds visit the river island near Mandagadde. 

The butterfly diversityinvestigations in Tiger-Lion safari Thyaverekoppa, revealed the presence of 57 species of butterflies, representing 5 familiesPramod Kumar et.al, 2007. Papilionidae is represented by 5 genera and   10 species; Lycaenidae by 8 genera each with one species. Nymphalidae by 21 genera with 28 species; Pieridae by 7 genera and 8 species and hesperidae by 3 genera each with one species. The checklist of all species observed is given in Table 2.

Table 2: Butterflies along with their status in the Tiger-Lion safari, Thyavarekoppa

Sl.No. Scientific name Common name Status
Family Papilionidae
1 Graphium agamemnon (Linnaeus) Tailed Jay C
2 Graphium nomius (Esper) Spot Swordtail C
3 Graphium sapedon (Linnaeus) Common Blue Bottle R
4 Pachlioopta aristolochiae(Linnaeus) Common Rose R
5 Pachlioopta hector (Linnaeus) Crimson Rose* VC
6 Pachlioopta pandiyana (Moore) Malabar Rose* R
7 Papilio demoleus (Linnaeus) Lime Butterfly VC
8 Papilio polymnestor (Cramer) Blue Mormon** R
9 Papilio polytes (Linnaeus) Common Mormon C
10 Troides minos (Cramer) Southern Birdwing* R
Family : Lycaenidae
11 Alphnaeus vulcanus (Fabricius) Common Silverline R
12 Arhopala amantes (Hewitson) Large Oak Blue R
13 Castalius rosimon (Fabricius) Common Pierrot VC
14 Discolampa ethion (Westwood) Banded Blue Pierrot C
15 Jamides bochus (Stoll) Dark Cerulean C
16 Lampides boeticus (Linnaeus) Pea blue C
17 Talicada nyseus (Guerin-Meneville) Red Pierrot C
18 Zizeeria karsandra (Moore) Common dark Grass Blue VC
Family: Nymphalidae
19 Acraea violae (Fabricius) Tawny Coster VC
20 Ariadne merione (Cramer) Common Castor R
21 Byblia ilithyia (Drury) Jocker C
22 Cupha erymanthis (Drury) Rustic C
23 Danaus chrysippus (Linnaeus) Plain Tiger R
24 Danaus genutia (Cramer) Striped Tiger C
25 Euploea core(Cramer) Common Indian Crow VC
26 Hypolomnas bolina (Linnaeus) Great Eggfly R
27 Hypolomnas misippus(Linnaeus) Danaid eggfly** C
28 Junonia almana (Linnaeus) Peacock Pansy R
29 Junonia atlites (Linnaeus) Gray Pansy R
30 Junonia hierta (Fabricius) Yellow Pansy C
31 Junonia iphita (Cramer) Chocolate Pansy C
32 Junonia lemonias (Linnaeus) Lemon Pansy VC
33 Junonia orithya (Linnaeus) Blue Pansy C
34 Lethe rohria (Fabricius) Common tree brown R
35 Melanitis leda (Linnaeus) Common Evening Brown VC
36 Moduza procris (Cramer) Commander R
37 Mycalesis patnia (Moore) Glade eye Bush brown** R
38 Mycalesis perseus (Fabricius) Common Bush brown C
39 Neptis hylas (Moore) Common Sailer VC
40 Orsotrioena medus( Fabricius) Nigger C
41 Phalanta phalantha (Drury) Common Leopard VC
42 Polyura athamas (Drury) Common Nawab R
43 Symphaedta nais (Forster) Baronet** VC
44 Tanaecial lepidea (Butler) Grey Count R
45 Tellewo limniace (Cramer) Blue Tiger VC
46 Ypthima baldus (Fabricius) Common Four Ring VC
Family: Pieridae
47 Anaphaeis aurota(Fabricius) Pioneer VC
48 Catopsilia pomona (Fabricius) Common Emigrant C
49 Catopsilia pyranthe(Linnaeus) Mottled Emigrant VC
50 Colotis danae (Fabricius) Crimson Tip R
51 Delias eucharis (Drury) Common Jezebel** R
52 Eurema hecabe (Linnaeus) Common Grass Yellow VC
53 Hebomoea glaucippe (Linnaeus) Great Orange Tip R
54 Valeria valeria (Joicey & Talbot) Common Wanderer C
Family : Hesperiidae
55 Borbo cinnara (Wallace) Rice Swift C
56 Gangara thyrsid (Fabricius) Gaint Red Eye R
57 Spialia galba (Fabricius) Indian Skipper R
VC - Very Common; C-Common; R- Rare
* - Endemic to Western Ghats; ** - Endemic to Peninsular India and Sri Lanka.

Animals (Karnataka forest Department, 2006):  22 species of mammals (Table 3), 42 birds (Table 4), 10 reptiles (Table 5), 6 Amphibians (Table 6) and 16 fishes (Table 7) have been reported from the Sanctuary (Source: Shimoga wildlife division).

  • Prey animals: Spotted deer, Sambar, Indian Gaur,Indian wild Boar, Indian porcupine, Hare and common langurs.
  • Predators: Panthers, Tigers, Indian wild dogs, Pythons and King Cobras, Jackals, Hyenas and vultures.
  • Other Animals:Elephants, Sloth bear, Malbar Squirrel, Monkeys, Tortoise.

Table 3: Mammals of Shettihalli wildlife Sanctuary

Sl. No. Species name Common names
1 Macaca sinica The Bonnet monkey
2 Pithecus entellus Hanuman monkey
3 Loris lydekkerianus Slender loris
4 Felis affinis The tiger
5 Felis affinis The Jungle cat
6 Acinonyx venaticus The hunting leopard
7 Mangos mungo mungo Indian mungoose
8 Canis indicus The Indian Jackal
9 Lutra lutra The common Otter
10 Melurus ursinus The sloth bear
11 Tragullus meminna Mouse deer
12 Pteropus giganteus The Indian flying fox
13 Lyroderma lyra lyra Vampire bat
14 Petaurista philippensis South Indian flying squirrel
15 Seiurus malabaricus The Malabar Squirrel
16 Seirus The Bison
17 Muntiacus vaginalis The barking deeer
18 Rosa unicolor The sandbur
19 Axis The spotted deer
20 Sues cryostats The Indian Wild Boar
21 Hystrix leucra The Indian Porcupine
22 Manis crassicaudata The Indian Pangolin

Table 4: Birds of Shettihalli Wildlife Sanctuary

Sl. No. Species name Common Name
1 Corvus macrorhynchos Jungle Crow
2 Palaeornis torquatus Common Indian parrot
3 Neopharon ginginianus Vulture
4 Haliastur indus Brahminy kite
5 Crocopus chlorogaster Green pigeon
6 Columba intemedia Blue rock pigeon
7 Pavo cristatus Pen fowl
8 Gallus sonnerati Gray jungle fowl
9 Gallooerdix spadicea Red Sour Fowl
10 Francolinus pondicerians Gray patridge
11 Sarkidiornis melanotos Comb Duck
12 Dendrocygna javanica The Whistling teal
13 Nettium crecea Common teal
14 Gallus bankiva murgi Red jungle fowl
15 Dendrocitta rufa Tree pie
16 Dumetia hyperithra The Rufous-Hellied Babbler
17 Otocompusa jocose fascucaudata Southern Red Whiskered Bul Bul
18 Saxicolodes cambaiensis India Robin
19 Pycnonotus luteolus White browed bulbul
20 Terpsiphone paradisi Paradise flycatcher
21 Cyornis tickellioe Blue flycatcher
22 Tephrodornis pondiceriana common  woodshrike
23 Pericocotus speciosus The Scarlet minivet
24 Dicururus macrocerus The king Crow
25 Dissemurus sctorius The Rocket tailed drongo
26 Orthotomus sctoricus The Tailor Bird
27 Acredotheres trestis  The Common myna
28 Gymnoris xanthocolis Yellow throated Sparrow 
29 Hirindo rustica The Common Sallow
30 Hirundo filifera Wire tailed Swallow
31 Dicoem erythrorthyncum Tikells Flower peacker
32 Leopicus blanfordil Yellow frinted pied wood pecker
33 Centropus parroti Southern crow pheasant
34 Alcedo benghalensis Common king fisher
35 Sarcogyps calvus Black Vulture
36 Astur dussumier The Indian shikhara
37 Oenopopelia transquebarica The red turtle dove
38 Amauromis phoenicurus The white breasted water hen
39 Bulbulcus coromandus Cattle egret
40 Nettion crecca The common teal
41 Demdrocygna javanica common whistling teal
42 Niroca rufa The white Bye

Table 5: Reptiles found in Shettihalli Wildlife Sanctuary

Sl. No. Species name Common Name
1 Crocodilus palustris The Mugger
2 Testudo elegans The land Tortoise
3 Gonotodes mysorenisi The Monitor lizard
4 Calotes versicolor  
5 Chameleon calcaratus Chameleon
6 Python molures Python
7 Tropidinotus stolatus Common Green Snake
8 Bugarus coeruleus Krait
9 Naja tripudians Cobra
10 Vipera resselli Viper King cobra

Table 6: Amphibians of Shettihalli Wildlife Sanctuary

Sl. No. Species name Common Name
1 Rana hexadactyla Green tank frog
2 Rana tigrina Bull frog
3 Rana cyanophlyctis Skipper frog
4 Rana malabarica The Tree frog
5 Rhacophorus pleuroxtictus Tree frog
6 Rana verrucosa kalloula The Plantain frog

Table 7: Fishes of Shettihalli Wildlife SanctuarySanctuary

Sl. No. Species name Common Name
1 Clarias batrachus The Black cat fish
2 Saccobranchus fossillis Scorpin fish
3 Wallago attu  
4 Callichrous bimaculatus Butter fish
5 Pseudotropius atheronoides Lady fish
6 Macrones vittatus Pidler
7 Macrenes ao  
8 Macrenes kelitius  
9 Barbus tor  
10 Barbus neilli  
11 Berbus sarana  
12 Labeo kontius  
13 Labeo boga  
14 Mastocembalus armatus  
15 Ophioce halus puntatus  
16 Oleucopunctatus gachua  

Social Aspects: The sanctuary has 32 enclosures and 70 villages inside the sanctuary. The size of the revenue enclosure varies from few house hold to a maximum of 110 household.95% of the people are dependent on agriculture. There are about 383 families and 616.18 Ha of encroachment before 1978 and 1292 families and 989.43 Ha after 1978 within the sanctuary, totally occupying 1605.61 Ha of the forest. (Karnataka forest Department, 2006).

Encroachment: There are about 383 families and 616.18 Ha of encroachment before 1978 and 1992. 989.46 Ha after 1978 within the sanctuary who occupied 1605.61 Ha. (Karnataka forest Department, 2006)

Park Zonations:The Sanctuary is classified into zones as per the norms, for better management of the sanctuary. The details of Zonations are as follows:

  • Core Zone: This Zone comprises part of Hanagere state forest and part of Shankar state forest, excluding the enclosures. The area of core zone is 100.60 Sq.Km.
  • Buffer Zone: This Zone includes Purdal state forest, part of Anesara and Shankar state forest, entire Sacrebyle, Kudi and Kumadwathi state forests, Harohithlu, Masarur, Baruve, Mugudthi state forests. Excluding enclosure the total area of buffer zone is 237.4 Sq.Km.
  • Tourism Zone: It includes parts of Shankar, Kudi, Sacrebyle and Kumdwathi state forests. Tourism zone also includes Lion safari at Thyavarekoppa, Elephant camp at Sacrebyle and Bird Sanctuary at Mandagadde. The total area is 57.60 Sq.Kms.

Tourism: The following are the existing tourism facilities:

  1. Tiger and Lion safari, Thyavarekoppa: Tiger and lion Safari was established in the year 1988 at Thyavarekoppa. A safari park is a place of education, enterainment and enlightment and a breeding place of endangered species. The total extent of safari is 195.0 hectares.
  2. Sacrebyle elephant camp: It is situated on Shimoga-Mangalore highway and it is 14 Kms from Shimoga city. There are 19 elephants and 2 calves at present.
  3. Mandagadde Bird Sanctuary: It is about 30 Kms from Shimoga on the left side of Shimoga-Tirthahalli main road.This is an island in Thunga River and 1.14 Acre in extent. This ia a place for the migratory birds which come for breeding and feeding.

6.3 SHARAVATHI VALLEY WILDLIFE SANCTUARY

Geographically Sharavathi Valley Wildlife Sanctuarylocated between  13°  54’   to 14˚ 12’ North and  74° 38’   to 75˚ 00’ Eastin central Western Ghats region of Karnataka state (Figure 2).Sharavathi Valley Wildlife Sanctuary was notified vide Government order No. AFD70/FWL71/ Dated 20.04.1972 and has an area of 431.23 Sq. Kms. with a final notification No. AFD/12/FWL/74 Dated 27.06.1974. It is spread over in the Sharavathi River Valley of Sagar Taluk in Shimoga District. The area of the Sanctuary is 431.23 Sq. Kms out of which an area of 123.63 Sq. Kms is under the water spread of Sharavathi Reservoir. The Sanctuary lies in the Western Ghats, mainly covered with evergreen and semi-evergreen forests in the valleys and grassy patches on hill tops, and are immensely rich in flora and fauna both in variety and diversity. The boundaries of the sanctuary are as follows: Jog S.F., Thalakalale Reservoir and Karagal S.F. form the northern boundary of the Sanctuary.Eastern boundary of Sharavathi Reservoir forms the Eastern boundary of the Sanctuary. The southern part consists of Mukambika Wildlife Sanctuary and North Canara District boundary. Common boundary of Shimoga and North Canara district forms Western boundary of the Sanctuary. The area is highly undulating with altitudinal range of 94 mts. MSL at Nagavalli to 1102 mts. MSL at Edigudda and consists of valleys and hillocks. The area is marked by perennial nalas and a large number of small streams. The forests are rich with evergreen and semi evergreen species and dense undergrowth.The climate is of monsoon type. The intensity of rain fall is more during June to September by the regular south west monsoon. The break of the monsoon is attended by high velocity wind. The temperature varies from 11˚ C to 38˚ C depending upon the factor of elevation.The rainfall, particularly during monsoon, is very heavy. The sanctuary is exposed to torrential showers during April, May and October with heavy showers in June, July and August. The erosive action of the torrential rain can be noticed in open areas. In areas devoid of vegetation cover the, top soil gets washed out with water resulting in unproductive, barren lateritic surfaces. The average rainfall of the area is 4500 mm.

Brief history

This sanctuary area previously came under the control of the princely State of Mysore. The MysoreKingdom had shown keen interest towards the protection of forests, and for better management of forests and wild-life, all the forest areas had been declared as State Forests during 1905-1940. Since then, these forests have been managed in a systematic way for fulfilling the needs of people.During 1964-65, Linganamakki dam was constructed across the Sharavathi River which led to submersion of many villages and forest areas. The people affected by this hydro-electric project were shifted from the project area and allowed to settle in various other places. After the submersion of forest area many big and small Islands has created. The study of these Islands shows good vegetation due to least biotic pressure and inaccessible. There are 31 Islands found in the sanctuary (Karnataka forest Department, 2006).


Figure 2.1: Sharavathi Valley Wildlife Sanctuary

After the enactment of the Wildlife (protection) Act, 1972 and Forest Conservation Act, 1980, more emphasis has been given for protection of wildlife and in creating awareness among the people about the need to conserve wildlife. Then onwards the protection and development activities towards the better management of wildlife in the sanctuary were commenced and continued by the wildlife wing of the Forest Department. With the handing over of the sanctuary areas to the wildlife wing by the territorial wing, these activities have been further intensified in a systematic way.Thewildlife division has been functioning independently since 01.08.1993 after taking over of 6 State Forests, submersion area and islands, from Sagar Territorial Division. Details of State Forests and other areas coming under Sharavathi Valley Wildlife Sanctuary are given in Table 81.

Table 8.1:Details of forests in Sharavathi valley wildlife sanctuary

Sl. No. Name of the forest Legal status Block No. Compartment No. Area in Ha.
1 Govardhanagiri SF XX 1–34 (34) 13473.68
2 Karini SF XXI 1-17 (17) 5102.53
3 Muppane Bl. A SF XIX 4,5,6,7 (4) 961.77
4 Muppane Bl. B SF XIX 8,9,10,11 (4) 629.16
5 Channagonda (part) SF XIX 13 (part) 701.05
6 Attigodu SF XIX 1,2,3 (3) 763.70
7 Submerged area       12363.00
8 Islands       507.00
9 Others       8621.11
  TOTAL       43123.00

Land-use analysis was done using maximum likelihood classifier and percentage compositions of various categories of land-use are listed in Table 8.2; the same is depicted in Figure 2.2. The forest cover in the sanctuary is about 49.5% and 17.6% is water body at full level of the reservoir.

Table 8.2: Land-use analysis (%area) in SVWS.

Classification Area (%)
Built-up 8.62
Evergreen to semi-evergreen 35.63
Moist-deciduous 13.84
Plantation (Areca/Acacia/Casuarina) 15.27
Water body 17.64
Agriculture 2.66
Open land 6.35


Figure 2.2: Land-use in  Sharavathi Valley Wildlife Sanctuary

Vegetation types inside the sanctuary area including islands (in the reservoir) vary from grassland to evergreen forest. The vegetation type in the core zone and buffer zone varies from moist-deciduous to evergreen forest. But in few places, grasslands, especially on hill tops, are interspersed with evergreen forests. Scrub jungles to semi-evergreen forests are more prevalent in the tourist zone of the sanctuary. The species richness suggests that semi-evergreen forests have more species due to the combined presence of both evergreen and deciduous species. The evergreen forest in the sanctuary area is more fragmented and disturbed and this is clearly depicted in the Shannon’s diversity index. The percentage evergreenness and endemic plants are more in the evergreen forest area.

The sanctuary has a variety of habitats that support rich flora of herbs, shrubs and climbers of which about 215 species have been recorded. Evergreen to semi-evergreen forests and grasslands of the Western Ghats have the largest congregations of endemic herbs. Some of the herbs are exclusive to specialised habitats like tree trunks and wet rocks. The increasing human impact and openings in forest canopy as well as over grazing are posing threats to many of these rare plants.

Evergreen to semi-evergreen forests are the major source of perennial waters. On the other hand in the deciduous tract, the streams mostly dry up in the summer months. Therefore conservation of evergreen forests and restoration of such forests are of paramount importance. Bulk of the water flow into reservoir comes from natural forests. Unfortunately, in some parts of the sanctuary area, monoculture plantations have been raised causing the drying up of streams and impoverishment of the ecosystems as a whole. Since the plantations do not yield any fodder or NTFP, the rural population is put to great hardship. Therefore such land-uses are not desirable in the sanctuary area. The numerous streams and the banks of Sharavathi and Venkatapura rivers and their tributaries in the evergreen to semi-evergreen forest belt are lined with characteristic riparian vegetation of which the notable tree species are Calophyllum apetalum, Elaeocarpus tuberculatus, Mastixia arborea, Hydnocarpus laurifolia, Madhuca neriifolia, etc. Towards the drier forests, water bodies are lined with tree species such as Pongamia pinnata, Madhuca neriifolia, Hopea wightiana, Bambusa sp., etc. The riparian vegetation plays a crucial role in protecting the water bodies from siltation, creating shade conditions to maintain appropriate temperature regime for sustaining populations of endemic fishes, amphibians, phytoplankton, zooplankton and aquatic insects. Of late there has been numerous instances of misuse of the banks of streams and rivers in the catchment area causing severe upsets in the characteristic biota associated with them. Stream waters are often diverted to newly created horticultural farms, thereby,  affecting the water flow into the reservoir. During field observations, it was noticed that the endemic vegetation patches were associated with perennial streams. The estimated basal area per hectare is highest for evergreen forests and is decreasing from semi-evergreen to scrub. But higher Shannon diversity for semi-evergreen compared to evergreen, may be due to disturbances and canopy openings, which pave way for the addition of some pioneers and other secondary species. Plant species of the sanctuary are listed in Table 8.3 and the percentage evergreens and percentage endemics range from evergreen towards moist deciduous (Table 8.4).

Table 8.3: Plant species in SVWS

Species name Family Habit Distribution
Abrus pulchellus Faboideae Climber Oriental and Paleotropic
Abutilon persicum Malvaceae Shrub Oriental-Indomalaysia
Acanthospermum hispidum Asteraceae Herb Neotropic
Achyranthus aspera Amaranthaceae Herb Pantropical
Acronychia pedunculata Rutaceae Tree Oriental-Indomalaysia
Actinodaphne hookeri Lauraceae Tree Oriental-W. Ghats
Adhatoda zeylanica Acanthaceae Shrub Oriental-Indomalaysia
Aeginetia indica Orobanchaceae Herb Indomalaysia to Japan
Aerides maculosum Orchidaceae Herb Oriental-W. Ghats
Aeschynomene aspera Faboideae Herb Paleotropics
Aganosma cymosa Apocynaceae Climber Oriental-India, Sri Lanka
Aglaia anamallayana Meliaceae Tree Oriental-W. Ghats
Aglaia roxburghiana Meliaceae Tree Oriental-Indomalaysia
Aglaia sp(bark not red) Meliaceae Tree  
Aglaia sp (red bark big leaf) Meliaceae Tree  
Alangium salvifolium Alangiaceae Straggler Oriental-W. Ghats
Allophylus cobbe Sapindaceae Shrub Oriental-S. India, Sri Lanka,
Alpinia malaccansis Zingiberaceae Herb Oriental-Indomalaysia
Alseodaphne semicarpifolia Lauraceae Tree Oriental-W. Ghats, Sri Lanka
Alstonia scholaris Apocynaceae Tree Oriental to Australian
Alysicarpus bupleurifolius Faboideae Herb Indomalaysia, China
Ammannia baccifera Lythraceae Herb Paleotropics
Amoora polystachia Meliaceae Tree Oriental-India, Sumatra
Amorphophallus bulbifer Araceae Herb India, Burma
Anamirta cocculus Menispermaceae Climber Oriental-Indomalaysia
Ancistrocladus heyneanus Ancistrocladaceae Climber Oriental-W. Ghats
Andrographis ovata Acanthaceae Herb  
Species name Family Habit Distribution
Angelonia biflora Scrophulariaceae Herb S America
Anisomeles indica Lamiaceae Undershrub Indomalaysia, China
Annonaceae member Annonaceae Climber  
Antidesma menasu Euphorbiaceae Tree Oriental-W. Ghats
Apama siliquosa Aristolochiaceae Shrub Oriental-W. Ghats, Sri Lanka
Aphyllorchis montana Orchidaceae Herb Oriental-W. Ghats
Ardisia solanacea Myrsinaceae Shrub Oriental-Peninsular India
Arenga wightii Arecaceae Palm Oriental-W. Ghats
Argostemma courtallense Rubiaceae Herb Oriental-W. Ghats
Argostemma verticillatum Rubiaceae Herb Oriental-India
Arisaema tortuosum Araceae Herb Oriental- Himalayas, W.Ghats
Aristolochia indica Aristolochiaceae Climber Oriental-India, Sri Lanka
Artabotrys zeylanicus Annonaceae Sca.shrub Oriental-W. Ghats, Sri Lanka
Artocarpus gomezianus Moraceae Tree Oriental-W. Ghats, Sri Lanka
Artocarpus heterophyllus Moraceae Tree Oriental-W. Ghats
Artocarpus hirsutus Moraceae Tree Oriental-W. Ghats
Asclepiadaceae member_1 Asclepiadaceae Climber  
Asclepias curassavica Asclepiadaceae Herb Neotropic
Asparagus racemosus Liliaceae Climber Palaeotropics
Asystasia crispata Acanthaceae Herb  
Atalantia wightii Rutaceae Tree Oriental-W. Ghats, Sri Lanka
Bacopa monnieri Scrophulariaceae Herb Tropics
Bambusa arundinaceae Poaceae Reed Oriental-Throughout India
Bauhinia racemosa Faboideae Tree Oriental-Indomalaysia, China
Begonia integrifolia Begoniaceae Herb Oriental-W. Ghats
Begonia malabarica Begoniaceae Herb Oriental-W. Ghats
Beilschmiedia fagifolia Lauraceae Tree Oriental-W. Ghats
Bhidea burnsiana Poaceae Herb Oriental-Peninsular India
Bidens biternata Asteraceae Herb Asiatic
Biophytum sensitivum Oxalidaceae Herb Western peninsular India, Sri Lanka
Bischofia javanica Euphorbiaceae Tree Oriental-Indomalaysia
Species name Family Habit Distribution
Blachia denudata Euphorbiaceae Shrub Oriental-W. Ghats
Blepharis asperrima Acanthaceae Herb Western India
Boehmeria glomerulifera Urticaceae Climber Oriental-Indomalaysia
Boehmeria platyphylla Urticaceae Herb South west India, Sri Lanka
Boesenbergia pulcherrima Zingiberaceae Herb Oriental-W. Ghats
Bombax ceiba Bombacaceae Tree Oriental-Indomalaysia
Breynia retusa Euphorbiaceae Shrub Oriental-India, Sri Lanka
Bridelia scandens Euphorbiaceae Shrub Oriental-W. Ghats
Buchanania lanzan Anacardiaceae Tree Oriental-India, Myanmar
Burmannia coelestis Burmanniaceae Herb Oriental-Indomalaysia
Butea monosperma Faboideae Tree Indomalaya
Calamus sp. Arecaceae Climber Oriental-W. Ghats
Calicopteris floribunda Combretaceae Climber Oriental-Indomalaysia
Callicarpa tomentosa Verbenaceae Tree Oriental-South India
Calophyllum apetalum Clusiaceae Tree Oriental-W. Ghats
Calophyllum tomentosum Clusiaceae Tree Oriental, Paleoarctic
Calotropis gigantea Asclepiadaceae Climber Tropical Asia
Calycopteris floribunda Combretaceae Straggler Oriental-Indomalaysia
Canarium strictum Burseraceae Tree Oriental-W. Ghats
Canscora decurrens Gentianaceae Herb Oriental-W. Ghats
Canscora decussata Gentianaceae Herb Tropical Africa, Madagascar, India
Canscora perfoliata Gentianaceae Herb Oriental-W. Ghats
Canthium dicoccum Rubiaceae Tree South India, Myamnar
Canthium parviflorum Rubiaceae Shrub Oriental-W. Ghats
Capparis rheedei Capparaceae Sca.shrub Oriental-W. Ghats
Carallia brachiata Rhizophoraceae Tree Oriental to Australian
Careya arborea Lecythidaceae Tree Oriental-Himalayas to Sri Lanka
Carissa inermis Apocynaceae Sca.shrub Oriental-Peninsular India
Caryota urens Arecaceae Tree Oriental-W. Ghats
Casearia Sp. Flacourtiaceae Tree  
Caseria rubescens Flacourtiaceae Tree Oriental-W. Ghats
Species name Family Habit Distribution
Cassia fistula Faboideae Tree Oriental-China, Indomalaysia
Cassia mimosoides Faboideae Herb Tropics
Cassia tora Faboideae Herb Tropics
Cassine glauca Celastraceae Tree Oriental-Indomalaysia
Cayratia trifolia Vitaceae Climber India, Ceylon, Malacca
Celosia argentea Amaranthaceae Herb Tropics
Celtis cinnamomea Ulmaceae Tree Oriental-Indomalaysia
Centella asiatica Apiaceae Herb Tropics
Centranthera indica Scrophulariaceae Herb Oriental-Indomalaysia
Cestrum nocturnum Solanaceae Sca.shrub West Indies
Chasalia ophioxyloides Rubiaceae Shrub South India, Sri Lanka
Chlorophytum orchidastrum Liliaceae Herb India, Tropical Africa
Chrysophyllum roxburghii Sapotaceae Tree Oriental-Indomalaysia
Cinnamomum macrocarpum Lauraceae Tree Oriental-W. Ghats
Cinnamomum zeylanicum Lauraceae Tree Oriental-Indomalaysia
Cissus discolor Vitaceae Climber Oriental-Indomalaysia
Cissus repens Vitaceae Climber Indomalaysia, Nepal to Taiwan, Java
Cleidion javanicum Euphorbiaceae Tree Oriental-Indomalaysia
Cleisostoma tenuifolium Orchidaceae Herb Oriental-W. Ghats
Clerodendrum paniculatum Verbenaceae Shrub Oriental-Indomalaysia
Clerodendrum serratum Verbenaceae Shrub Oriental-India, Sri Lanka
Clerodendrum viscosum Verbenaceae Shrub Oriental-Indomalaysia
Coldenia procumbens Boraginaceae Herb Pantropical
Combretum latifolium Combretaceae Climber Oriental-Indomalaysia
Commelina benghalensis Commelinaceae Herb Paleotropics
Connarus wightii Connaraceae Sca.shrub Oriental-W. Ghats
Corchorus trilocularis Tiliaceae Herb Oriental-Tropical India
Costos speciosus Costaceae Herb Oriental-Indomalaysia
Cottonia peduncularis Orchidaceae Herb Oriental-W. Ghats, Sri Lanka
Crotolaria filipes Faboideae Herb Oriental-W. Ghats
Crotolaria pallida Faboideae Shrub Oriental,Paleotropic, Neotropic
Species name Family Habit Distribution
Crotolaria retusa Faboideae Shrub Oriental,Paleotropic, Neotropic
Crotolaria verrucosa Faboideae Herb Oriental,Paleotropic, Neotropic
Croton gibsonianus Euphorbiaceae Shrub Oriental-W. Ghats
Curculigo orchioides Liliaceae Herb India, Java
Curcuma neilgherrensis Zingiberaceae Herb Oriental-W. Ghats
Cyathocline purpurea Asteraceae Herb Oreintal-India, Myamnar
Cyathula prostrata Amaranthaceae Herb Paleotropics
Cyclea peltata Menispermaceae Climber Oriental-W. Ghats
Cymbidium aloifolium Orchidaceae Herb Oriental-Indomalaysia, Indochina
Cynoglossum zeylanicum Boraginaceae Herb Oriental-South India, Sri Lanka
Cyrtococcum oxyphyllum Poaceae Herb Oriental-Indomalaysia
Dalbergia Sp. Faboideae Climber  
Dalbergia sympathetica Faboideae Climber Oriental-W. Ghats
Dendrobium macrostachyum Orchidaceae Herb Oriental-India, Sri Lanka
Dendrobium nanum Orchidaceae Herb Oriental-W. Ghats
Dendrobium ovatum Orchidaceae Herb Oriental-W. Ghats
Derris canarensis Faboideae Climber Oriental-W. Ghats
Desmodium laxiflorum Faboideae Shrub Oriental-Indomalaysia
Desmodium triflorum Faboideae Herb Tropics
Desmodium triquetrum Faboideae Shrub Indomalaysia, China
Desmos lawii Annonaceae Straggler Indomalaysia, China
Dichapetalum gelonioides Dichapetalaceae Shrub Oriental-W. Ghats
Dictyospermum ovalifolium Commelinaceae Herb Oriental-W. Ghats
Dillenia pentagyana Dilleniaceae Tree Oriental- China to Indomalaysia
Dimocarpus longan Sapindaceae Tree Oriental-Tropics
Dimorphocalyx beddomei Euphorbiaceae Tree Oriental-W. Ghats
Dioscorea bulbifera Dioscoreaceae Climber Oriental-India, Sri Lanka
Dioscorea oppositifolia Dioscoreaceae Climber Oriental-India, Sri Lanka
Diospyros assimilis Ebenaceae Tree Oriental-W. Ghats
Diospyros buxifolia Ebenaceae Tree Oriental-Indomalaysia
Diospyros candolleana Ebenaceae Tree Oriental-W. Ghats
Species name Family Habit Distribution
Diospyros crumenata Ebenaceae Tree Oriental-Western Karnataka, Sri Lanka
Diospyros melanoxylon Ebenaceae Tree Oriental-Peninsular India,
Diospyros montana Ebenaceae Tree Oriental to Tropical Australia
Diospyros nigrescens Ebenaceae Tree Oriental-W. Ghats
Diospyros pruriens Ebenaceae Tree Oriental-W. Ghats
Diospyros Sp. Ebenaceae Tree  
Dipterocarpus indicus Dipterocarpaceae Tree Oriental-W. Ghats
Dopatrium junceum Scrophulariaceae Herb Oriental-Indomalaysia
Dracaena terniflora Agavaceae Herb Oriental-India, S.E. Asia
Drosera burmanii Droseraceae Herb West Africa to North east Africa
Drosera indica Droseraceae Herb Tropical Africa to Australia
Duranta repens Verbenaceae Shrub South America
Dysoxylum glandulosum Meliaceae Tree Oriental-W. Ghats
Ecbolium ligustrinum Acanthaceae Shrub Oriental-India, Sri Lanka
Eclipta alba Asteraceae Herb Pantropical
Elaeagnus conferta Elaeagnaceae Tree Oriental-Indomalaysia
Elaeocarpus serratus Elaeocarpaceae Tree Oriental-India
Elaeocarpus tuberculatus Elaeocarpaceae Tree Oriental-Indomalaysia
Elatostema cuneatum Urticaceae Herb Oriental-India, Sri Lanka
Elatostema lineolatum Urticaceae Herb Oriental-India
Elephantopus scaber Asteraceae Herb Pantropical
Emblica officinalis Euphorbiaceae Tree Palaeotropics
Emilia sonchifolia Asteraceae Herb Pantropical
Entada pursaetha Faboideae Climber Oriental-Western India,
Epaltes divaricata Asteraceae Herb W Peninsular India, China, Myanmar
Epipogium roseum Orchidaceae Herb W Africa, Indomalaysia
Epithema carnosum Gesneriaceae Herb Oriental-W. Ghats
Eria dalzelli Orchidaceae Herb Oriental-W. Ghats
Eriocaulon stellulatum Eriocaulaceae Herb Oriental-W. Ghats
Eriocaulon xeranthemum Eriocaulaceae Herb Tropical Africa, Oriental-India
Ervatamia heyneana Apocynaceae Tree Oriental-W. Ghats
Species name Family Habit Distribution
Euodia lunu-ankenda Rutaceae Tree Oriental-India to S. E. Asia
Euonymus indicus Celastraceae Tree Oriental-W. Ghats
Eupatorium odoratum Asteraceae Herb Neotropic
Euphorbia hirta Euphorbiaceae Herb Pantropical
Euphorbia notoptera Euphorbiaceae Herb Oriental-W. Ghats
Euphorbia thymifolia Euphorbiaceae Herb Tropics
Evolvulus alsinoides Convolvulaceae Herb Paleotropics
Evolvulus nummularius  Convolvulaceae Herb Tropical America
Exacum bicolor Gentianaceae Herb Oriental-Peninsular India
Exacum carinatum Gentianaceae Herb Oriental-Central India, W. Ghats
Exacum lawii Gentianaceae Herb Oriental-W. Ghats, Sri Lanka?
Exacum pedunculatum Gentianaceae Herb Oriental- India
Ficus arnottiana Moraceae Tree Oriental-Deccan Peninsula, Sri Lanka
Ficus asperrima Moraceae Tree Oriental-India, Sri Lanka
Ficus heterophylla Moraceae Tree Oriental-India, Sri Lanka,
Ficus hispida Moraceae Tree Oriental-Indomalaysia
Ficus nervosa Moraceae Tree Oriental-India to Vietnam
Ficus Sp. Moraceae Tree  
Fimbristylis camplanata Cyperaceae Herb Pantropical
Flacourtia montana Flacourtiaceae Tree Oriental-W. Ghats
Flemingia strobilifera Faboideae Shrub Oriental-Indomalaysia
Garcinia gummi-gutta Clusiaceae Tree Oriental-W. Ghats, Sri Lanka
Garcinia indica Clusiaceae Tree Oriental-W. Ghats, Sri Lanka
Garcinia morella Clusiaceae Tree Oriental-Indomalaysia
Garcinia talbotii Clusiaceae Tree Oriental-W. Ghats
Geissaspis cristata Faboideae Herb Oriental-W. Ghats
Geophila reniformis Rubiaceae Herb Oriental-India, Sri Lanka
Globba marantina Zingiberaceae Herb Oriental- India, Sri Lanka, Malaya
Glochidion sp. Euphorbiaceae Tree  
Glochidion zeylanicum Euphorbiaceae Tree Oriental-Indomalaysia
Gloriosa superba Liliaceae Climber Paleotropics
Species name Family Habit Distribution
Glycosmis pentaphylla Rutaceae Shrub Oriental-S. India, Sri Lanka
Gnetum ula Gnetaceae Climber Oriental-South India
Gnidia glauca Thymelaeaceae Shrub Palaeotropics
Goniothalamus cardiopetalus Annonaceae Tree Oriental-W. Ghats
Gordonia obtusa Theaceae Tree Oriental-W. Ghats
Grangea maderaspatana Asteraceae Herb Paleotropics
Grewia disperma Tiliaceae Tree Paleotropics, Oriental-India, Myanmar
Grewia microcos Tiliaceae Tree Oriental-Asia
Grewia tiliifolia Tiliaceae Tree Tropical Africa, Tropical
Grewia umbellifera Tiliaceae Sca.shrub Oriental-Central and Peninsular India
Grewilia robusta Gymnosperm Tree  
Gymnema sylvestre Asclepiadaceae Climber Paleotropics, Oriental
Gymnosporia rothiana Celastraceae Shrub Oriental-W. Ghats
Gymnostachyum latifolium Acanthaceae Shrub Oriental-W. Ghats
Habenaria crinifera Orchidaceae Herb Oriental- W. Ghats, Sri Lanka
Habenaria grandifloriformis Orchidaceae Herb Oriental-Deccan, W Peninsular India
Habenaria longicorniculata Orchidaceae Herb Oriental- W. Ghats
Harpullia imbricata Sapindaceae Tree Oriental-Indomalaysia
Hedyotis caerulea Rubiaceae Herb Oriental- South India
Hedyotis corymbosa Rubiaceae Herb  
Hedyotis herbacea Rubiaceae Herb Paleotropic
Hedyotis nitida Rubiaceae Herb Oriental- W. Ghats, Sri Lanka
Helicteres isora Sterculiaceae Shrub Oriental- Indomalaysia
Heliotropium indicum Boraginaceae Herb Pantropical
Heliotropium marifolium Boraginaceae Herb Indomalaysia
Hemidesmus indicus Asclepiadaceae Climber Oriental-India, Sri Lanka
Hibiscus furcatus Malvaceae Sca.shrub Tropical Africa, Tropical Asia
Hippocratea indica Hippocrataceae Climber Oriental-Indomalaysia
Holarrhena antidysenterica Apocynaceae Tree Oriental-India, Malaya
Holigarna arnottiana Anacardiaceae Tree Oriental-W. Ghats
Holigarna beddomii Anacardiaceae Tree Oriental-W. Ghats
Species name Family Habit Distribution
Holigarna ferruginea Anacardiaceae Tree Oriental-W. Ghats
Holigarna grahamii Anacardiaceae Tree Oriental-W. Ghats
Hopea parviflora Dipterocarpaceae Tree Oriental-W. Ghats
Hopea wightiana Dipterocarpaceae Tree Oriental-W. Ghats
Hoya ovalifolia Asclepiadaceae Herb Oriental- Peninsular India, Sri Lanka
Hoya retusa Asclepiadaceae Herb Oriental- W. Ghats
Hybanthus enneaspermus Violaceae Herb Africa to Australia
Hydnocarpus laurifolia Flacourtiaceae Tree Oriental-W. Ghats
Hydrocotyl javanica Apiaceae Herb Tropical Africa-Indomalaysia
Hydrocotyl sibthorpioides Apiaceae Herb Tropical Africa-Indomalaysia
Hygrophila auriculata Acanthaceae Herb Oriental-India, Sri Lanka
Hypoxis aurea Hypoxidaceae Herb Oriental-India, S.E. Asia
Hyptis suaveolens Lamiaceae Herb Tropical America
Ichnocarpus frutescens Apocynaceae Climber Indomalaysia, Australia
Impatiens balsamina Balsaminaceae Herb Indomalaysia, China
Impatiens oppositifolia Balsaminaceae Herb Oriental- W. Ghats, Sri Lanka
Impatiens scapiflora Balsaminaceae Herb Oriental- W. Ghats
Impatiens trichocarpa Balsaminaceae Herb Oriental- W. Ghats
Iphigenia indica Liliaceae Herb Oriental-Indomalaysia
Ipomoea hederifolia Convolvulaceae Twiner Tropical America
Ischaemum indicum Poaceae Herb Oriental-South India
Ixora arborea Rubiaceae Tree Oriental-W. Ghats
Ixora brachiata Rubiaceae Tree Oriental-W. Ghats
Ixora coccinea Rubiaceae Shrub Oriental-W. Ghats, Sri Lanka
Ixora polyantha Rubiaceae Shrub Oriental- W. Ghats
Jasminum malabaricum Oleaceae Climber Oriental-W. Ghats
Jasminum ritchiei Oleaceae Climber Oriental-W. Ghats, Sri Lanka
Jasminum rottlerianum Oleaceae Climber Oriental-W. Ghats
Jerdonia indica Gesneriaceae Herb Oriental- W. Ghats
Justicia betonica Acanthaceae Herb Tropical Africa, India, Sri Lanka, Malaysia
Justicia simplex Acanthaceae Herb E Africa, India, Malaysia
Species name Family Habit Distribution
Knema attenuata Myristicaceae Tree Oriental-W. Ghats
Knoxia sumatrensis Rubiaceae Herb Oriental-Indomalaysia
Lagenandra meeboldii Araceae Herb Oriental- W. Ghats
Lagerstroemia microcarapa Lythraceae Tree Oriental-W. Ghats
Lagerstroemia parviflora Lythraceae Tree Oriental-W. Ghats, Myanmar
Lannea coromandelica Anacardiaceae Tree Oriental-India, Sri Lanka
Leea indica Leeaceae Shrub Oriental- India, China to Australia
Lepisanthes tetraphylla Sapindaceae Tree Oriental-W. Ghats, Sri Lanka, Myanmar
Leucas biflora Lamiaceae Herb Oriental-W Peninsular India, Sri Lanka
Leucas ciliata Lamiaceae Herb Oriental-India
Leucas hirta Lamiaceae Herb Oriental-South India
Leucas lavandulifolia Lamiaceae Herb Oriental-Indomalaysia
Leucus marrubioides Lamiaceae Herb Oriental-W. Ghats, Sri Lanka
Limnophila aromatica. Scrophulariaceae Herb Tropical India, N Australia
Limnophila indica Scrophulariaceae Herb Paleotropics
Lindernia anagallis Scrophulariaceae Herb Oriental-Indomalaysia
Lindernia antipoda Scrophulariaceae Herb Oriental-Indomalaysia
Lindernia ciliata Scrophulariaceae Herb Oriental-Indomalaysia
Lindernia hyssopoides Scrophulariaceae Herb Oriental-India, Sri Lanka
Lindernia nummulariifolia Scrophulariaceae Herb Oriental-India, Myanmar
Lindernia procumbens Scrophulariaceae Herb Temperate to tropical Eurasia
Lindernia pusilla Scrophulariaceae Herb Paleotropics
Lindernia rotundifolia Scrophulariaceae Herb Oriental-W and S. India, Sri Lanka, Madagascar
Linociera malabarica Oleaceae Tree Oriental-W. Ghats
Litsea laevigata Lauraceae Tree Oriental-W. Ghats
Litsea sp. Lauraceae Tree  
Lobelia alsinoides Campanulaceae Herb Oriental-S and S.E. Asia
Lobelia nicotianifolia Campanulaceae Herb Oriental-Indomalaysia
Lophopetalum wightianum Celastraceae Tree Oriental-Indomalaysia
Ludwigia perennis Onagraceae Herb Indomalaysia, E Africa, Iran, Sri Lanka
Luvunga sarmentosa Rutaceae Shrub Oriental-Java, Sri Lanka
Species name Family Habit Distribution
Macaranga peltata Euphorbiaceae Tree Oriental-W. Ghats, Sri Lanka
Madhuca latifolia Sapotaceae Tree Oriental- India, Myanmar
Malaxis acuminata Orchidaceae Herb Oriental-Indomalaysia
Malaxis rheedii Orchidaceae Herb India, Thailand, China
Mallotus philippensis Euphorbiaceae Tree China, Indomalaysia to Australia
Mangifera indica Anacardiaceae Tree Oriental-W. Ghats
Mastixia arborea Cornaceae Tree Oriental-W. Ghats
Mecardonia procumbens Scrophulariaceae Herb Neotropic
Melastoma malabathricum Melastomataceae Shrub Oriental-India
Melochia corchorifolia Sterculiaceae Herb Tropics
Memecylon sp. Melastomataceae Shrub  
Memecylon talbotianum Melastomataceae Tree Oriental-W. Ghats
Memecylon terminale Melastomataceae Shrub Oriental-W. Ghats
Memecylon umbellatum Melastomataceae Tree Oriental-W. Ghats, Sri Lanka
Memecylon wightii Melastomataceae Shrub Oriental-W. Ghats
Menispermaceae member Menispermaceae Climber  
Mesua ferrea Clusiaceae Tree Oriental-Indomalaysia
Mimosa pudica Faboideae Herb Tropical America
Mimusops elengi Sapotaceae Tree Oriental-Indomalaysia
Mitraphora heyneana Annonaceae Tree Oriental-W. Ghats
Mollugo pentaphylla Molluginaceae Herb Paleotropics
Monochoria vaginalis Pontederiaeae Herb Paleotropics
Moullava spicata Faboideae Sca.shrub Oriental- W. Ghats
Murdannia pauciflora Commelinaceae Herb Oriental-S. India, Malaya
Murdannia semiteres Commelinaceae Herb Africa, S. India
Murdannia simplex Commelinaceae Herb Paleotropics
Murraya koenigii Rutaceae Tree Oriental-India, Sri Lanka
Murraya paniculata Rutaceae Shrub Oriental-Indomalaysia
Mussaenda bellila Rubiaceae Sca.shrub Oriental-Peninsular India
Myristica dactyloides Myristicaceae Tree Oriental-W. Ghats, Sri Lanka
Myristica malabarica Myristicaceae Tree Oriental-W. Ghats
Species name Family Habit Distribution
Naravelia zeylanica Ranunculaceae Climber Oriental-India, Sri Lanka, Java
Naregamia alata Meliaceae Herb Oriental-India, Angola
Neanotis foetida Rubiaceae Herb Oriental- W. Ghats
Neolitsea scrobiculata Lauraceae Tree Oriental-Western India
Nothapodytes nimmoniana Icacinaceae Tree Oriental-China, Indomalaysia
Nothopegia colebrookeana Anacardiaceae Tree Oriental-W. Ghats
Nymphaea nouchali Nymphaeaceae Herb Tropics
Nymphaea pubescens Nymphaeaceae Herb Tropics
Nymphoides aurantiaca Menyanthaceae Herb Oriental-S. India, Sri Lanka
Nymphoides indica Menyanthaceae Herb Oriental-Indomalaysia
Oberonia brunoniana Orchidaceae Herb Oriental- W. Ghats
Oberonia santapaui Orchidaceae Herb Oriental- W. Ghats
Olax wightiana Olacaceae Sca.shrub Oriental- W. Ghats, Sri Lanka
Olea dioica Oleaceae Tree Oriental-N E India, S W India
Ophiorrhiza hirsutula Rubiaceae Herb Oriental-W. Ghats
Osbeckia truncata Melastomataceae Herb Oriental- W. Ghats
Oxalis corniculata Oxalidaceae Herb Pantropical
Pajanelia longifolia Bignoniaceae Tree Oriental-India, Myanmar
Palaquium ellipticum Sapotaceae Tree Oriental-W. Ghats
Pandanus Sp. Pandanaceae Shrub  
Paramignya monophylla Rutaceae Climber Oriental-India, Sri Lanka
Paspalum scrobiculatum Poaceae Herb Oriental- India
Passiflora subpeltata Passifloraceae Climber Native of Madagascar
Pavetta indica Rubiaceae Shrub Oriental-South India
Pennisetum pedicellatum Poaceae Herb India, Tropical Africa
Peperomia pellucida Piperaceae Herb S America
Peperomia portulacoides Piperaceae Herb Madagascar to S W India
Peristylus aristatus Orchidaceae Herb Oriental-India, Sri Lanka
Peristylus secundus Orchidaceae Herb Oriental-S. India
Persea macarantha Lauraceae Tree Oriental-South India, Sri Lanka
Phaulopsis imbricata Acanthaceae Herb India, Africa, Sri Lanka, Madagascar
Species name Family Habit Distribution
Phoebe cathia Lauraceae Tree Oriental-W. Ghats, C Himalayas to Myanmar
Phoenix humilis Arecaceae Palm Oriental-W. Ghats
Pholidota pallida Orchidaceae Herb Oriental-Indomalaysia
Phyllanthus debilis Euphorbiaceae Herb India, Tropical Africa
Phyllanthus niruri Euphorbiaceae Herb Tropics except Australia
Phyllanthus urinaria Euphorbiaceae Herb Tropics
Pinanga dicksonii Arecaceae Palm Oriental-W. Ghats
Piper nigrum Piperaceae Climber Oriental-E and W. Ghats
Plantanthera susannae Orchidaceae Herb Oriental-Indomalaysia
Plectranthus mollis Lamiaceae Herb Oriental-India
Plectranthus stocksii Lamiaceae Herb Oriental-Central and S. India
Plumbago zeylanica Plumbaginaceae Herb Tropics
Poeciloneuron indicum Clusiaceae Tree Oriental-W. Ghats
Polyalthia fragrance Annonaceae Tree Oriental-W. Ghats
Polygonum chinense Polygonaceae Herb Oriental-Indomalaysia
Polystachya flavescens Orchidaceae Herb Oriental-Indomalaysia
Porpax jerdoniana Orchidaceae Herb Oriental- W. Ghats
Porpax reticulata Orchidaceae Herb Oriental- W. Ghats
Portulaca oleracea Portulacaceae Herb Tropics
Pothos scandens Araceae Climber Oriental-India, Sri Lanka,
Pouzolzia zeylanica Urticaceae Herb China through Indomalaysia
Prunus ceylanica Rosaceae Tree Oriental-South India to S.E. Asia
Psychotria canarensis Rubiaceae Shrub Oriental-W. Ghats
Psychotria dalzellii Rubiaceae Shrub Oriental-W. Ghats
Psychotria flavida Rubiaceae Shrub Oriental-W. Ghats
Psychotria truncata Rubiaceae Shrub Oriental-W. Ghats
Pterocarpus marsupium Faboideae Tree Oriental-W. Ghats, Sri Lanka
Pterospermum acerifolium Sterculiaceae Tree Oriental-Indomalaysia
Pterospermum diversifolium Sterculiaceae Tree Oriental-W. Ghats, Java, Philippines, Malaysia
Ramphicarpa longiflora Scrophulariaceae Herb Oriental- W. Ghats
Randia rugulosa Rubiaceae Sca.shrub Oriental- W. Ghats, Sri Lanka
Species name Family Habit Distribution
Randia uliginosa Rubiaceae Shrub Oriental-India, Myanmar
Rauvolfia serpentina Apocynaceae Shrub India, Sri Lanka, Java
Rhynchoglossum notonianum Gesneriaceae Herb Oriental- W. Ghats, Sri Lanka
Rhynchospora wightiana Cyperaceae Herb Oriental- W. Ghats
Rhynchostylis retusa Orchidaceae Herb Oriental-Indomalaysia
Rotala densiflora Lythraceae Herb Oriental-Indomalaysia
Rotala macrandra Lythraceae Herb Oriental-S. India
Rubia cordifolia Rubiaceae Climber Palaeotropics
Rungia pectinata Acanthaceae Herb Oriental-India, Sri Lanka, Myanmar
Sageraea laurifolia Annonaceae Tree Oriental-W. Ghats
Salomonia ciliata Polygalaceae Herb India, Sri Lanka, Malaya, Australia
Santalum album Santalaceae Tree Oriental-South India
Saraca asoca Faboideae Tree Oriental-Indomalaysia
Sarcostigma kleinii Euphorbiaceae Climber Oriental-Eastern & W. Ghats
Schefflera venulosa Araliaceae Tree Oriental-India, Myanmar,
Schleichera oleosa Sapindaceae Tree Oriental-Indomalaysia
Scoparia dulcis Scrophulariaceae Herb Neotropic
Scutia myrtina Rhamnaceae Shrub Oriental-Myanmar, India
Sebastania chamaela Euphorbiaceae Herb Paleotropics
Sida acuta Malvaceae Herb Pantropical
Sida cordifolia Malvaceae Herb Pantropical
Sida rhombifolia Malvaceae Herb Oriental-Indomalaysia
Smilax zeylanica Smilacaceae Climber Oriental-South E. Asia to
Smithia conferta Faboideae Herb Oriental-Indomalaysia
Smithia hirsuta Faboideae Herb Oriental- W. Ghats
Solanum americanum Solanaceae Herb Temperate and Tropical
Solanum surattense Solanaceae Herb Indomalaya, Tropical Australia, Polynesia
Solanum violaceum Solanaceae Herb Tropical Africa, Indian subcontinent
Sophubia delphinifolia Scrophulariaceae Herb Oriental-S. India, Sri Lanka
Spermacoce articularis Rubiaceae Herb Oriental-Indomalaysia
Spermacoce mauritiana Rubiaceae Herb Pantropical
Species name Family Habit Distribution
Spermacoce pusilla Rubiaceae Herb Paleotropics
Spermacoce verticillata Rubiaceae Herb Pantropical
Stachytarpheta indica Verbenaceae Herb Tropical America
Sterculia guttata Sterculiaceae Tree Oriental-W. Ghats, Sri Lanka
Steriospermum personatum Bignoniaceae Tree Oriental-India, Myanmar,
Striga angustifolia Scrophulariaceae Herb Oriental-Indomalaysia
Striga asiatica Scrophulariaceae Herb Paleotropics
Striga densiflora Scrophulariaceae Herb Oriental-Central and S. India
Strobilanthus barbatus Acanthaceae Shrub Oriental-W. Ghats
Strobilanthus heyneanus Acanthaceae Shrub Oriental-W. Ghats
Strobilanthus integrifolius Acanthaceae Shrub Oriental-W. Ghats
Strombosia ceylanica Olacaceae Tree Oriental-W. Ghats
Strychnos dalzelli Loganiaceae Climber Oriental-Peninsular India
Swertia corymbosa Gentianaceae Herb Oriental- W. Ghats
Symplocos racemosa Symplocaceae Tree Oriental-W. Ghats
Syzygium caryophyllatum Myrtaceae Tree Oriental-W. Ghats, Sri Lanka
Syzygium cumini Myrtaceae Tree Oriental-Indomalaysia
Syzygium gardnerii Myrtaceae Tree Oriental-W. Ghats, Sri Lanka
Syzygium laetum Myrtaceae Tree Oriental-W. Ghats
Syzygium macrocephala Myrtaceae Tree Oriental-W. Ghats
Syzygium Sp.1 Myrtaceae Tree  
Syzygium Sp.2 Myrtaceae Tree  
Tarenna asiatica Rubiaceae Shrub Oriental-Indomalaysia
Tephrosia pulcherrima Faboideae Herb Oriental-W. Ghats, Sri Lanka
Terminalia alata Combretaceae Tree Oriental-India
Terminalia bellirica Combretaceae Tree Oriental-Indomalaysia
Terminalia chebula Combretaceae Tree Oriental-India, Myanmar
Terminalia paniculata Combretaceae Tree Oriental-Peninsular India
Tetrameles nudiflora Datiscaceae Tree Oriental-India, Sri Lanka,
Thunbergia mysorensis Acanthaceae Climber Oriental-W. Ghats
Toddalia asiatica Rutaceae Climber Oriental-South India
Species name Family Habit Distribution
Tolypanthus lagenifer Loranthaceae Shrub Oriental- W. Ghats
Toona ciliata Meliaceae Tree India to Australia
Torenia bicolor Scrophulariaceae Herb Oriental- W. Ghats
Tragia hispida Euphorbiaceae Twiner Oriental-Peninsular India
Trapa natans Trapaceae Herb Oriental-India, Sri Lanka
Trewia nudiflora Euphorbiaceae Tree Oriental-India, Sri Lanka
Tricalysia apiocarpa Rubiaceae Tree Oriental-W. Ghats
Tricholepis glaberrima Asteraceae Herb Oriental-India
Triumfetta rhomboidea Tiliaceae Herb Tropical Africa, Asia
Turnera ulmifolia Turneraceae Herb  
Turraea villosa Meliaceae Shrub Western peninsular India, Java
Tylophora indica Asclepidiaceae Climber Oriental-Indomalaysia
Unidentified (from Chikmattur)   Tree  
Unidentified (from Karni)   Tree  
Unidentified (from Mayyalli)   Tree  
Unidentified (from Talgani)   Tree  
Urena lobata Malvaceae Herb Pantropical
Utricularia aurea Lentibulariaceae Herb Oriental and Australian
Utricularia praeterita Lentibulariaceae Herb Oriental-S. India
Utricularia reticulata Lentibulariaceae Herb Oriental-India, Sri Lanka
Utricularia striatula Lentibulariaceae Herb Paleotropics
Uvaria narum Annonaceae Climber Oriental-W. Ghats, Sri Lanka
Vangueria spinosa Rubiaceae Tree Oriental-Indomalaysia
Ventilago madraspatana Rhamnaceae Climber Oriental-W. Ghats, Sri Lanka, Java
Vepris bilocularis Rutaceae Tree Oriental-W. Ghats
Vernonia cineria Asteraceae Herb Paleotropics
Vitaceae member Vitaceae Climber  
Vitex altissima Verbenaceae Tree Oriental- South India
Vitex negundo Verbenaceae Shrub Oriental-Asia
Vitis auriculata Vitaceae Climber Oriental- India
Wendlandia thyrsoidea Rubiaceae Tree Oriental-S. India, Sri Lanka
Species name Family Habit Distribution
Xantolis tomentosa Sapotaceae Tree Oriental-India,China
Xylia xylocarpa Faboideae Tree Oriental-Indomalaysia
Xyris pauciflora Xyridaceae Herb Oriental-Indomalaysia
Zanthoxylum ovalifolium Rutaceae Shrub Oriental-Singapur
Zanthoxylum rhetsa Rutaceae Tree Oriental-Indomalaysia
Zingiber cernum Zingiberaceae Herb Oriental-W. Ghats
Zingiber neesanum Zingiberaceae Herb Oriental-W. Ghats
Ziziphus oenoplia Rhamnaceae Sca.shrub Pantropics
Ziziphus rugosa Rhamnaceae Straggler Oriental-India, Sri Lanka
Zornia gibbosa Faboideae Herb Tropics
       
Sca.shrub-Scandent Shrub      

Table 8.4: Details of different landscape elements sampled and their diversity indices, basal area, percentage evergreens and percentage endemics.

Vegetation type Total transects Total quadrats Total area sampled (ha.) Total individuals Total species Estimated basal area/ha. Species richness Shannon’s diversity Simpson’s diversity % Evergreens % Endemics
20 96 11.8 1818 128 35.3 17 3.94 0.96 95.8 56.7
Semi-evergreen 16 82 3.3 1916 138 31.1 18 4.03 0.97 77.1 40.9
Moist deciduous 3 18 0.7 318 58 19.8 10 3.44 0.95 43.6 19.7
Scrub 2 5 0.2 6 4 0.6 2 1.24 0.67 0.0 0.0

Lichens

Lichens are unique groups of plants exhibiting symbiotic association of fungi and algae, but represented as a single organism. Because of their sensitivity to microclimatic changes in environment, lichens aid as bioindicators. They require specific conditions in the environment and respond critically to any changes in it. Hence, they are widely used in air pollution, geochemical and geothermal emission, and biomonitoring studies. They play various roles as pioneers in successionaland climax ecosystems and could as well indicate the age and ecological continuity of a forest. Apart from this, they also can be used as tools in determining the age of an unknown rock surface (lichenometry) and soil formation (pedogenesis) during plant succession. Western Ghats harbour 800 species of lichens in which, 161 species are endemic to this region. The study in SVWS shows the presence of 46 species of lichens in the SVWS (in semi-evergreen forest of Holebagilu, Honnemaradu Island, Karumane, Muppane and Siganduru) representing 5% from the Western Ghats of Karnataka. (Table 8.4). However, lichen studies need to be carried out more intensively. Table 8.5 gives Simpson’s and Shannon-Weiner’s diversity indices. Holebagilu and Karumane are highly diverse, while Honnemaradu (Island) is least diverse in lichen composition.

Table 8.4: Lichen species recorded in SVWS

Taxa Growth form Holebagilu Siganduru Muppane Karumane Honnemardu (I) Substrata
Arthoniaceae              
Cryptothecialunulata (Zahlbr.) Makhija & Patwardhan C + +   +   16,27,33,41
C. phyctidiforme (Müll. Arg.) Awasthi & K Singh C     +     1,4,47
C. stirtonii A.L. Smith C +       + 5,13,34
C.subnidulans Stirton C         + 5,11,34,39,41
Arthopyreniaceae              
Arthopyrenia indusiata Müll. Arg. C +         1,12,24,27,31,35,39,51
A. subnexa (Nyl.) Müll. Arg. C +         1,5,24,27,30
A. terminata (Nyl.) Müll. Arg. C + +   +   4,8,14,27,
Bacidiaceae              
Bacidia incongruens (Stirton) Zahlbr. C       +   2,22,39
B. subletorum (Schreber) Lettau C     +     36
Taxa Growth form Holebagilu Siganduru Muppane Karumane Honnemardu (I) Substrata
Brigantiaea leucoxantha (Sprengel) Half. In Half & Bellem C +         15,25,48
Caliciales (Order)              
Heterocyphelium leucompyx (Tuck.) Vainio C +         1,6
Catilariaceae              
Catilaria pulverea (Borrer) Lattau C         + 1,6,8,9,18,19,45,48
Coccocarpiaceae              
Coccocarpia erythroxyli (Sprengel) Swinsc and Krog. F   +   + + 2,4,5,14,20,22,23,27,32, 37,39,40,41, 44,48,50
Collamataceae              
Leptogium aurstro-americanum (Malme) Dodge F   +   +   3,4,7,20,37,39,41,44,46, 47,50,
L. denticulatum Nyl. F     + +   2,3,10,41,42,44,50
Graphidaceae              
Graphina petricosa (Krempelh) A. Zahlbr. C       +   2,4,39,41
Graphis nakanishiana Patwardhan & Kulkarni C     +   + 4,10,14,18,20,39,44,49
Taxa Growth form Holebagilu Siganduru Muppane Karumane Honnemardu (I) Substrata
Xylographa vitiligo (Ach.) Laundon C     + + + 2,4,10,14,16,20,27,28,30,
41,44
Lecanoraceae              
Lecidia sp1 C +         2,12
Lecidia sp2 C     +     2,4
Lecidia sp3 C       +   4,45
Lecidia sp4 C +   +   + 2,13,16,27,34,45,46
Letrouitiaceae              
Letrouitia trangressa (Malme) Half. & Bellem C     +     2,4,36,48
Opegraphaceae              
Opegrapha subvulgata Nyl. C +         6
Pertusariaceae              
Ochrolechia androgyna (Hoffm.) Arnold C   +       23
O. subviridis (Hoeg) Erichsen C +         6,27,40
Pertusaria albescens (Huds.) M. Choisy & Werner C     +     2,42
P. multipunctata (Turner) Nyl. C     +     2
Phyllosporaceae              
Phyllospora  manipurensis (Müll. Arg.) Sch. F +   +     2,27
P. parvifolia (Pers.) Müll. Arg. F + + +     2,12,23,31,37,38,43
Taxa Growth form Holebagilu Siganduru Muppane Karumane Honnemardu (I) Substrata
Physciaceae              
Physcia aipolia (Ehrh. in Humb.) Furnr F +         13,31
P. dimidiata (Arn.) Nyl. F   +       1,2,18,29
Pilocarpaceae              
Byssoid sp1 C + +   +   1,2,4,12,14,20,21,25,27,32,38,39,41,50
Pyrenulaceae              
Pyenula mamillana (Ach.) Trevisan C + +       2,8,5,17,27
Pyrgillus sp. C   +       41
Teloschistaceae              
Caloplaca ferruginea (Huds.) Th. Fr. C +   +     2,10,13,15,27,39,44
Thelotremataceae              
Ocellularia allosporoides (Nyl.) Patwardhan and Kulkarni C   +       2,4,6,24,25,27,31,35,40,50,
O. groenhartii Hale C +         1,12,14,15,16,19,23,27,30,
36,38,39,40
Thelotrema leprocarpum (Nyl.) Tuck. C   + +   + 5,14,18,34,44,45,48
Trichotheliaceae              
Porina interestes (Nyl.) Harm C + +       1,8,27,31,44
P. internigrans (Nyl.) Müll. Arg. C + +   +   2,4,13,15,30,39,41,44
Taxa Growth form Holebagilu Siganduru Muppane Karumane Honnemardu (I) Substrata
P. subcutanea Ach. C +         17,27,38
P. subhibernica Upreti C +   +   + 4,5,6,10,11,12,13,16,17,20, 21, 23,24,26,27,29,31, 37,40,44,50,51,52
Trypthilliaceae              
Trypthelium tropicum (Ach.) Müll. Arg. C         + 11

Note: C – Crustose, F – Foliose

Substratum of the Lichen Species

No. Substratum No. Substatum No. Substratum
1 Fallen twig 2 Unidentified tree 3 Rock
4 Aglaia elaegnoidea 5 Aporosa lindleyana 6 Artocarpus integrifolius
7 Artocarpus Sp. 8 Canarium strictum 9 Careya arborea
10 Cinnamomum Sp. 11 Diospyros condollena 12 Diospyros crumenata
13 Diospyros microphylla. 14 Diospyrus Sp. 15 Dysoxylun Sp.
16 Elaeagnus latifolia. 17 Elaeocarpus serratus 18 Ervatamia heyneana
19 Ficus asperrima. 20 Ficus Sp. 21 Garcinia morella
22 Garcinia talbotii 23 Holigarna arnottiana 24 Holigarna grahamii
25 Holigarna Sp. 26 Homalium zeylanicum 27 Hopea wightiana
28 Ixora brachiata. 29 Ixora parviflora 30 Ixora Sp.
31 Knema attenuata 32 Lagestroemia lanceolata 33 Linociera malabarica
34 Litsea laevigata 35 Mangifera indica 36 Memecylon terminale
37 Mimusops elengi 38 Myristica malabarica 39 Olea dioica
40 Polyalthia Sp. 41 Pterospermum reticulatum 42 Salle (Kannada name)
43 Strychnos nux-vomica 44 Syzygium Sp. 45 Terminalia arjuna
46 Terminalia chebula 47 Terminalia Sp. 48 Terminalia tomentosa
49 Toddalia asiatica 50 Ventalago maderaspatana 51 Vepris Sp.
52 Ziziphus jujuba      

Table 8.5 Simpson’s (D) and Shannon-Weiner’s (H’) indices for the lichens of studied localities


Locality

D

H’

Honnemaradu (Island)

1.26

1.397

Muppane

1.21

1.548

Karumane

1.14

1.675

Holebagilu

1.11

1.969

Siganduru

1.08

1.502

RANGE OF WILDLIFE, STATUS, DISTRIBUTION AND HABITAT

Forest type and cover: The biotic facing and edaphic variations have played a dominant role in determining the nature of the forests growing in the sanctuary. This sanctuary consists of multitiered vegetation that belongs to tropical evergreen type to moist deciduous type with lower, middle, top canopies, under growth and climbers. There are few areas where human interference is very low. On the fringes of villages the forest area has been degraded due to human interference as well as cattle pressure.Two types of forests are mainly found in sanctuary are:

  • Southern Tropical evergreen type: This type is seen in Nagavalli, Kannor Kote, part of Biligar and Kattinkar areas. The top canopy consists of Depterocarpus indicus, Calophyllum tomentosum, Machilus mecarantha,   Acrocarpus,   fraxinopolius,   Bischfia Javanica,   Syzigium Species,   Alstonia   scholaris,    Mangifera     indica.Second canopy consists of caryota   urens,    Aporasa   lindleyanaetc.
  • Southern Tropical Semi-Evergreen type:This type of forest is seen in parts of Muppane, Attigodu Satate Forests. The important species found are, Lagertroemia lanceolata,Careya arborea,Emblica officinalis, Randia species, Syzygium species, Terminalia species, Vitex   altisima, Mangifera indica, Artocarpus species and Bamboos in patches.

 

Animals: There are several kinds of animals in the sanctuary including carnivores, herbivores, omnivores and aquatic animals. The following are the important wild animals found in the sanctuary.

  • Carnivores:  Tiger (Panthera tigris), Panther (Normal and Black)   (Panthera pardus), Wild Dogs (Cuon alpines), Wild cats (Felis chaus), Malabar civets (Viverricule indica), Hyena           (Hyena hyena)
  • Herbivores: Sambar (Cervus unicolor),Barking Deer (Muntiocus muntjack), Spotted Deer (Axis axis), Zusk Deer (Moschus moschiferus), Black naped hare (Lepus nigricolis), The gaur (Bision) (Bos gaurus), Mouse Deer (Tragulus meninna).
  • Scvangers:Jackal (Canis aurus)
  • Reptiles:  Land monitor lizard (Veranus grisens), Python (Python molurus), King Cobra (Naja naja), Tortoises (Geochelone elegars)
  • Other Animals: Flying Squirrel (Refuta indica), Giant malabar squirrel (Benus hylopetus), Indian Porcupine (Hystrix indica), Common langur(Presbytis enstellus), Bonnet monkey (Macaca radiate), Lion tailed maeaque (Macaca slenus),Sloth bear (Melursus ursinus), Wild bear (Sus scrofa).

Butterflies
The Western Ghats comprises 330 species belonging to 166 genera and five families. It includes the largest butterfly, the Southern Birdwing (Troides minos) with a wingspan of about 140-190mm to the smallest, the Grass Jewel (Freyeria trochylus) and Tiny Grass Blue (Zizula hylax) with wingspan only 15-22 mm and 16-24 mm respectively. Nymphalidae and Lycaenidae are the major families that contribute to the entire Western Ghats butterfly species diversity. SVWS comprises five butterfly families with 173 species (Table 9.3). The family composition and the conservation status of the butterflies in Western Ghats are cited in Table 9.4.

Most of the Swallotails (Family; Papilionidae) show habitat preferences and hence can be used as indicators of ecosystem health. For instance, Spot Sword tail is found only in the thick evergreen forest and its larval host plants are Thottea siliquosa,etc., are found in the core and buffer zone of the sanctuary. The swallowtails are also found puddling near the streams.

The Brush-footed butterflies of the family Nymphalidae are represented by 65 species in the sanctuary. They are well distributed in the sanctuary area and some are habitat specific in nature. The Map Butterfly, Blue Nawab and Malabar Tree Nymph are found only in the moist and shady places. Blue Nawab is an endangered species encountered in Banukuli locality. Indian Sunbeam is found in moist places within the sanctuary area. Family Hesperiidae, popularly known as the family of “Skippers” comprises of tiny butterflies found throughout the sanctuary. Spotted Small Flat is endemic species found only in few localities.

Table 9.3: Butterflies species in SVWS

Species Common Name
Family: Papilionidae
Papilionidae: Papilioninae: Troidini
Troides minos Cramer Southern Birdwing (WG)
Pachliopta pandiyana Moore Malabar Rose (WG)
Pachliopta aristolochiae Fabricius Common Rose
Pachliopta hector L., Crimson Rose (PI&SL)*
Papilionidae: Papilioninae: Leptocircini
Graphium sarpedon L., Common Bluebottle
Graphium doson C&R Felder Common Jay
Graphium agamemnon L., Tailed Jay
Graphium nomius Esper Spot Sword Tail
Graphium antiphates Cramer Fivebar Swordtail
Papilionidae: Papilioninae: Papilioninii
Papilio clytia L., Common Mime
Papilio demoleus L., Lime Butterfly
Papilio liomedon Moore Malabar Banded Swallow Tail (WG)*
Papilio dravidarum Wood-Mason Malabar Raven (WG)
Papilio helenus L., Red Helen
Papilio polytes L., Common Mormon
Papilio polymnestor Cramer Blue Mormon (PI&SL)
Papilio paris L., Paris Peacock
Papilio buddha Westwood Buddha Peacock
Papilio crino Fabricius Common Banded Peacock
Family: Pieridae
Pieridae: Coliadinae: Coliadini
Catopsilia pomona Fabricius Common Emigrant
Catopsilia pyranthe L., Mottled Emigrant
Eurema brigitta Cramer Small Grass Yellow
Eurema laeta Boisduval Spotless Grass Yellow
Eurema hecabe L., Common Grass Yellow
Eurema blanda Boisduval Three-spot Grass Yellow
Eurema andersoni One spot Grass Yellow
Pieridae: Pierinae: Pierini
Delias eucharis Drury Common Jezebel (PI & SL)
Leptosia nina Fabricius Psyche
Pieris canidia L., Indian Cabbage White
Cepora nerissa Fabricius Common Gull
Anaphaeis aurota Fabricius Caper White or Pioneer
Appias indra Moore Plain Puffin
Appias libythea Fabricius Striped Albatross
Appias albina Boisduval Common Albatross
Colotis etrida Boisduval Small Orange Tip
Colotis eucharis Fabricius Plain Orange Tip
Colotis danae Fabricius Crimson Tip
Ixias marianne Cramer White Orange Tip
Ixias pyrene L., Yellow Orange Tip
Pieridae: Pierinae: Euchlocini
Pareronia valeria Cramer Common wanderer
Pareronia ceylanica C&R Felder Dark Wanderer (PI&SL)
Hebomoea glaucippe L., Great Orange Tip
Family: Nymphalidae
Nymphalidae: Satyrinae: Melanitini
Melanitis leda L., Common Evening Brown
Melanitis zitenius Herbst Great Evening Brown
Melanitis phedima Stoll Dark Evening Brown
Nymphalidae: Satyrinae: Elymniini
Elymnias hypermenstra L., Common Palmfly
Lethe europa Bamboo Tree Brown
Lethe rohria Common Tree Brown
Mycalesis anaxias Hewitson White-bar Bushbrown
Mycalesis mineus L., Dark-brand Bushbrown
Mycalesis perseus Fabricius Common Bushbrown
Mycalesis subditaMoore Tamil Bushbrown
Mycalesis patniaMoore Glad-eye Bushbrown (PI&SL)
Orsotrioena medus Fabricius The Nigger
Zipoetis saitis Tamil Catseye (WG)
Nymphalidae: Satyrinae: Satyrini
Ypthima asterope Klug Common Three-ring
Ypthima hiiebneri Kirby Common Four-ring
Ypthima baldus Fabricius Common Five-ring
Ypthima sp. Ring
Nymphalidae: Charaxinae: Charaxini
Polyura athamas Drury Common Nawab
Polyura schreiber Blue Nawab (PI&SL)*
Charaxes bernardus Tawny Rajah
Charaxes dolon Fabricius Black Rajah
Nymphalidae: Heliconiinae: Acraeini
Acraea violae Fabricius Tawny Coster
Nymphalidae: Heliconiinae: Heliconiini
Cethosia nietneri C&R Felder Tamil Lacewing (PI&SL)
Vindula erota Fabricius Cruiser
Nymphalidae: Heliconiinae: Argynnini
Cupha erymanthis Drury Rustic
Phalanta phalantha Drury Common Leopard
Cirrochroa thais Fabricius Tamil Yeoman (PI&SL)
Argyreus hyperbius L., Indian Fritillary
Nymphalidae: Aparturinae
Euripus consimilis Painted Courtesan
Nymphalidae: Limenitinae: Neptini
Neptis jumbahMoore Chestnut-streaked Sailer
Neptis hylasMoore Common Sailer
Pantoporia hordonia Stoll Common Lascar
Nymphalidae: Limenitinae: Limetini
Athyma perius L., Common Sergeant
Athyma nefte Colour Sargeant
Athyma ranga Moore Blackvein Sergeant
Limenitis procris Cramer Commander
Nymphalidae: Limenitinae: Parthenini
Parthenos sylvia Cramer Clipper
Nymphalidae: Limenitinae: Euthaliinii
Tanaecia lepidea Butler Grey Count
Euthalia aconthea Cramer Common Baron
Euthalia nais Forster Red Baron or Baronet (PI&SL)
Dolpha evelina Stoll Red-spot Duke
Nymphalidae: Limenitinae: Biblini
Byblia ilithyia Joker
Ariadne merione Cramer Common Castor
Ariadne ariadne L., Angled Castor
Nymphalidae: Limenitinae: Marpesiini
Cyrestis thyodamas Map
Nymphalidae: Libytheinae
Libythea lepitaMoore Common Beak
Nymphalidae: Nymphalinae: Nymphalini
Junonia hierta Fabricius Yellow Pansy
Junonia orithya L., Blue Pansy
Junonia lemonias L., Lemon Pansy
Junonia almana L., Peacock Pansy
Junonia atlites L., Grey Pansy
Junonia iphita Cramer Chocolate Pansy
Kaniska canace Blue Admiral
Cynthia cardui L., Painted Lady
Hypolimnas bolina L., Great Eggfly
Hypolimnas misippus L., Danaid Eggfly (PI&SL)*
Doleschallia bisaltide Autumn Leaf
Kallima horsfieldi Kollar South Indian Blue Oak Leaf (WG)
Nymphalidae: Danainae: Danaini
Parantica aglea Stoll Glassy Blue Tiger
Tirumala limniace Cramer Blue Tiger
Tirumala septentrionisButler Dark Blue Tiger
Danaus chrysippus L., Plain Tiger
Danaus genutia Cramer Striped Tiger
Nymphalidae: Danainae: Euploeini
Euploea core Cramer Common Indian Crow
Idea malabarica Moore Malabar Tree Nymph (WG)
Family: Lycaenidae
Lycaenidae: Riodininae: Riodinini
Abisara echerius Stoll Plum Judy
Lycaenidae: Miletinae: Spalgini
Spalgis epius West Wood Apefly
Lycaenidae: Polymmatinae: Polymmatini
Castalius rosimon Fabricius Common Pierrot
Caleta caleta Hewitson Angled Pierrot
Discolampa ethion Doubleday & Hewitson Banded Blue Pierrot
Leptotes plinius Fabricius Zebra Blue
Azanus ubaldus Bright Babul Blue
Everes lacturnus Godart Indian Cupid
Actolepis puspa Horsfield Common Hedge Blue
Neopithecops zalmoraButler Quaker
Pseudozizeeria maha Kollar Pale Grass Blue
Zizeeria karsandraMoore Dark Grass Blue
Zizina otis Fabricius Lesser Grass Blue
Zizula hylax Fabricius Tiny  Grass Blue
Chilades laius Stoll Lime Blue
Freyeria trochylus Freyer Grass Jewel
Lampides boeticus L., Pea Blue
Jamides bochus Cramer Dark Cerulean
Jamides celeno Cramer Common Cerulean
Jamides alecto Felder Metallic Cerulean
Nacaduba pactolus Large four line blue
Nacaduba hermus Pale-4 line Blue
Prosotas nora C & R Felder Common Lineblue
Prosotas dubiosa Tailless Lineblue
Talicada nyseus Guerin-Meneville Red Pierrot
Lycaenidae: Theclinae: Arhopalini
Arhopala amantes Hewitson Large Oakblue
Thaduka multicaudata Moore Many-tailed Oakblue
Lycaenidae: Theclinae: Amblypodiini
Iraota timoleon Stoll Silverstreak Blue
Amblypodia anita Hewitson Leaf Blue
Lycaenidae: Theclinae: Aphnaeini
Spindasis vulcanus Fabricius Common Silverline
Lycaenidae: Theclinae: Loxurini
Loxura atymnus Yamfly
Lycaenidae: Theclinae: Horagini

Rathinda amor

Monkey Puzzle

Lycaenidae: Theclinae: Hypolycaenini
Zeltus amasa Fluffy tit
Lycaenidae: Theclinae: Deudorigini
Deudorix epijarbas Cornelian
Deudorix isocrates Common Guva Blue
Rapala manea Hewitson Slate Flash
Rapala varuna Moore Indigo Flash
Lycaenidae: Curetinae
Curetis thetis Indian Sunbeam (PI&SL)
Family: Hesperiidae
Hesperiidae: Coeliadinae
Bibasis sena Moore Orange Tail Awl
Hasora chromus Cramer Common Banded Awl
Hasora badra Moore Common Awl
Badamia exclamationis Fabricius Brown awl
Hesperiidae: Pyrginae
Celaenorrhinus leucocera Kollar Common Spotted Flat
Celaenorrhinus ambareesa Moore Malabar Spotted Flat
Tagiades japetus Cramer Common Snow Flat
Tagiades litigiosa Moschler Water Snow Flat
Tagiades gana Moore Immaculate or Suffused Snow Flat
Pseudocoladenia dan Fabricius Fulvous Pied Flat
Coladenia indrani Moore Tricolor Pied Flat
Sarangesa dasahara Moore Common Small Flat
Sarangesa purendra Moore Spotted Small Flat (WG)
Odontoptilum angulatum C&R Felder Chestnut or Banded Angle
Spialia galba Fabricius Indian Grizzled Skipper
Hesperiidae: Hesperiinae
Ampittia dioscorides Bush Hopper
Halpe porus Moore's ace
Lambrix salsala Moore Chestnut Bob
Notocrypta paralysos Wood-Mason & de Niceville Common Banded Demon
Notocrypta curvifascia C & R Felder Restricted Demon
Udaspes folus Cramer Grass Demon
Suastus gremius Fabricius Indian Palm Bob
Suastus sp. Bob
Gangara thyrsis Fabricius Giant Redeye
Taractrocera maevius Fabricius Common Grass Dart
Talicota colon Fabricius Pale Palm Dart
Borbo cinnara Wallace Rice Swift
Pelopidas mathias Small branded swift
Note: * indicates Endangered species (Wildlife Protection Act, 1972)
WG – indicates Western Ghats endemic
PI&SL – indicates Endemic to Peninsular India and Sri Lanka.

Table 9.4:  Butterfly family composition in SVWS.

Family India Western Ghats Inside the sanctuary
Total species Endangered Western Ghats Endemics Shared Endemics (Western Ghats and Sri Lanka)
Papilionidae 107 19 19 2 5 3
Pieridae 109 33 23     2
Nymphalidae 520 96 65 2 3 6
Lycaenidae 450 101 38     1
Hesperiidae 320 81 28   1  

Molluscs

Molluscs are one of the most diverse groups of invertebrates - both in form and habitat. They have figured prominently in palaeobiological and biological studies, and have served as study organisms in numerous evolutionary, biomechanical, ecological, physiological, and behavioural studies. Many species of freshwater mussels and snails are threatened or endangered throughout the world. Twenty-one species belonging to 7 families were recorded from different localities. The list of species collected has been given in Table 9.5. The plight of freshwater mussels is a prime example of the decline of aquatic habitats and the species that inhabit them. If trends are not reversed and stream degradation and loss of habitat continues many of the interesting and beautiful molluscs will be lost forever.

Table 9.5:  Mollusc species in SVWS

Family Genera/Species
Cyclophoridae Alycaeus expatriatus
Cyclophoridae Cyclophorus jerdoni
Cyclophoridae Theobaldius Sp.
Cyclophoridae Craspedoptris Sp.
Cyclophoridae Cyathophoma Sp.
Diplommatinidae Nicida liricincta
Diplommatinidae Ophisthosoma deccanense
Ariophantidae Ariophanta immerita
Ariophantidae Ariophanta canarica
Ariophantidae Ariophanta Sp.
Ariophantidae Euplecta Sp.
Ariophantidae Macrochalmys Sp.
Helixarionidae Kaliella Sp.
Helixarionidae Kaliella sigurensis
Streptaxidae Streptaxis canarica
Subulinidae Glessula Sp. a
Subulinidae Glessula Sp. b
Subulinidae Glessula Sp. c
Subulinidae Glessula Sp. d
Subulinidae Opeas Sp.
Vertiginidae Pupisoma Sp.
Unidentified Unidentified

Reptiles

157 species of reptiles including a crocodile Crocodulus palustris is known from the Western Ghats. Out of 157 species 97 are endemics and majority of them are snakes. Twenty-three species of reptiles were recorded in the present study (Table 10.1). Three endemic species, viz., skink, malabar pit viper and bamboo pit viper were also recorded. Tortoises are commonly found in the reservoir. Crocodile (Crocodulus palustris) was recorded from reservoir at Madenur and Muppane area during the study. Two juveniles were caught in the nets of the fishermen at Holebagilu. There was an instance of livestock death due to crocodile at Muppane. King cobra is found in shady places and in the riparian vegetation dominated by Ochlandra sp. Malabar pit viper is found in between the buttresses of the huge trees of species like, Ficus nervosa, Syzigium gardneri and on the medium height shrubs. Hump nosed pit viper is found concealing in the litter cover.  

Table 10.1: Reptiles of SVWS

Common Name Scientific Name IUCN Status
Crocodile Crocodylus palustris VU
Common Indian Monitor Lizard Varnus bengalensis VU
Flapshell turtles Lissemys punctata Lr-lc
Indian Chameleon Chameleon zeylanicus VU
House Gecko Hemidactylus frenatus Lr-lc
Gunther’s Supple Skink *Lygosoma guentheri Lr-nt
King Cobra Ophiophagus hannah Lr-nt
The Cobra Naja naja Lr-nt
The Krait Bungarus caeruleus Lr-nt
Russell’s Viper Daboia russelli Lr-nt
Hump-nosed Pit Viper Hypnale hypnale Lr-nt
Saw Scaled Viper *Echis carinatus Lr-nt
Malabar Pit Viper *Trimersurus malabaricus Lr-nt
Bronzebacked Tree Snake Dendrelaphis tristis Lr-lc
The Vine Snake Ahaetulla nasuta Lr-nt
Flying Snake Chrysopelea ornata Lr-nt
Trinket Snake Elaphe helena helena Lr-nt
Checkered Keelback Xenochrophis piscator piscator Lr-lc
Montane Keelback *Amphiesma monticola Lr-nt
Common Sand Boa Eryx conicus conicus Lr-nt
Shieldtail *Uropeltis sp.  
The Rat Snake Ptyas mucosus Lr-nt
Python Python molurus Lr-nt
Note:   * Western Ghats endemic
VU – Vulnerable, LR-lc – Lower risk least concerned, LR-nt – Lower risk near threatened.

Avifauna

Birds are a unique group of vertebrates and can indicate the quality of habitat or environment. In the ecosystem studies, birds play a pivotal role as predators of lower organisms and prey to higher vertebrates. The bird diversity of an area not only indicates its health but also stability. A total of 122 bird species were sighted in the sanctuary area during the study period (Table 10.2). Inside the sanctuary, few localities are very important in bird diversity like, Muppane, Kanur and Govardhanagiri state forest. Muppane nature camp is an important area for bird watching as it is surrounded by heterogenous habitats from Scrub jungle to Semi-evergreen forest and also reservoir. The presence of some of the endemic and endangered species like, Malabar Grey Hornbill, and Great Indian Hornbill found in these areas signifies the presence of primary forest remnants. During the study, a flock of great Indian hornbill with 14 individuals were found in the Govardhanagiri forest. Apart from that, in some of the islands, malabar grey and Malabar Pied Hornbill are encountered which in turn shows the presence of endemic tree species, like, Myristica malabarica, Knema attenuata. In some of the forest enclosures the presence of green pigeons, hornbills and parakeets signifies also the presence of their foraging plant species.

Table 10.2: Birds of SVWS

Family Sub-family Common name Scientific name
Podicipitidae   Little grebe Podiceps ruficollis (Pallas)
Phalacrocoracidae   Large cormorant Phalacrocorax carbo L.,
    Little cormorant Phalacrocorax niger Vieillot
    Darter Anhinga rufa (Daudin)
Ardeidae   Night heron Nycticorax nycticorax L.,
    Purple heron Ardea purpurea L.,
Grey heron Ardea cinerea L.,
Paddy bird Ardeola grayii (Sykes)
    Cattle egret Bubulcus ibis L.,
    Median egret Egretta intermedia (Wagler)
    Little egret Egretta garzetta L.,
Ciconiidae   White necked stork Ciconia episcopus (Boddaert)
Threskiornithidae   White ibis Threskiornis aethiopica (Latham)
Accipitridae   Pariah kite Milvus migrans (Boddaert)
    Brahminy kite Haliastur indus (Boddaert)
    Shikra Accipiter badius (Gmelin)
    Tawny eagle Aquila vindhiana Franklin
    Crested serpent eagle Spilornis cheela (Latham)
    Indian griffon vulture Gyps fulvus (Hablizl)
Phasianidae   Grey jungle fowl Gallus sonneratii Temminck
    Red spurfowl Galloperdix spadicea (Gmelin)
    Common pea fowl Pavo cristatus L.,
Rallidae   White breasted waterhen Amaurornis phoenicurus (Pennant)
Jacanidae   Bronzewinged jacana Metopidius indicus Latham
Charadriidae Charadriinae Spotted sandpiper Tringa glareola L.,
    Little ringed plover Charadrius dubius Scopoli
    Redwattled lapwing Vanellus indicus (Boddaert)
    Yellowwattled lapwing Vanellus malabaricus (Boddaert)
Laridae   River tern Sterna aurantia J.E.Gray
Columbidae   Orangebreasted green pigeon Treron pompadora (Jerdon)
    Greyfronted green pigeon Treron pompadora (Gmelin)
    Green imperial pigeon Ducula aenea L.,
    Blue rock pigeon Columba livia (Gmelin)
    Spotted dove Streptopelia senegalensis (Scopoli)
    Emerald dove Chalcophaps indica L.,
Psittacidae   Roseringed parakeet Psittacula krameri (Scopoli)
    Blossomheaded parakeet Psittacula cyanocephala (L.,)
    Lorikeet Loriculus vernalis (Sparrman)
    Bluewinged parakeet Psittacula columboides (Vigors)*
Cuculidae   Cuckoo Cuculus canorus L.,
    Indian cuckoo Cuculus micropterus Gould
    Koel Eudynamys scolopacea L.,
    Sirkeer cuckoo Taccocua leschenaultii Lesson
    Crow-pheasant Centropus sinensis Stephens
Strigidae Striginae Forest eagle-owl Bubo nipalensis Hodgson
Trogonidae   Southern trogon Harpactes fasciatus (Pennant)
Alcedinidae   Small blue kingfisher Alcedo atthis L.,
    Whitebreasted kingfisher Halcyon smyrnensis L.,
    Small blue kingfisher Alcedo atthis (L.,)
    Pied kingfisher Ceryle rudis L.,
Meropidae   Chestnutheaded bee-eater Merops leschenaulti (Vieillot)
    Small green bee-eater Merops orientalis (Latham)
Upupidae   Hoopoe Upupa epops L.,
Bucerotidae   Common grey hornbill Tockus birostris (Scopoli)
    Malabar grey hornbill Tockus griseus Latham
    Great pied hornbill Buceros bicornis L., *
    Malabar pied hornbill Anthracoceros malabaricus Boddaert *
Capitonidae   Crimson throated barbet Megalaima rubricapilla Gmelin
    Small green barbet Megalaima viridis Boddaert
    Large green barbet Megalaima zeylanica Gmelin
Picidae   Indian goldenbacked threetoed woodpecker Dinopium javanense (Ljungh)
    Great black woodpecker Dryocopus javensis (Horsfield)
    Heartspotted woodpecker Hemicircus canente L.,
    Great black woodpecker Dryocopus javensis (Horsfield)
Alaudidae   Crested lark Galerida cristata (L.,)
Hirundinidae   Swallow Hirundo rustica  L.,
    Wiretailed swallow Hirundo smithii Leach
Oriolidae   Golden oriole Oriolus oriolus L.,
    Blackheaded oriole Oriolus xanthornus L.,
Daniidae   Rufousbacked shrike Lanius schach L.,
Dicruridae   Black drongo Dicrurus adsimilis (Bechstein)
    Racket-tailed drongo Dicrurus paradiseus L.,
Sturnidae   Brahminy myna Sturnus pagodarum (Gmelin)
    Rosy pastor Sturnus roseus L.,
    Indian myna Acridotheres tristis L.,
    Jungle myna Acridotheres fuscus (Wagler)
    Hill myna Gracula religiosa L.,
    Bank myna Acridotheres ginginianus (Latham)
Corvidae   House crow Corvus splendens Vieillot
    Tree pie Dendrocitta vagabunda (Latham)
Campephagidae   Scarlet minivet Pericrocotus roseus (Forster)
Irenidae   Iora Aegithina tiphia L.,
    Goldmantled chloropsis Chloropsis cochinchinensis (Gmelin)
    Fairy bluebird Irena puella (Latham)
Pycnonotidae   Redvented bulbul Pycnonotus cafer L.,
    Rubythroated bulbul Pycnonotus melanicterus gularis Gould
    Greyheaded bulbul Pycnonotus priocephalus Jerdon
    Redwhiskered bulbul Pycnonotus jocosus L.,
    Yellowbrowed bulbul Hypsipetes indicus (Jerdon)
Muscicapidae Timaliinae Common babbler Turdoides caudatus (Dumont)
    Rufous babbler Turdoides subrufus (Jerdon)
    Blackheaded babbler Rhopocichla atriceps
    Jungle babbler Turdoides striatus (Dumont)
    Slatyheaded scimitar babbler Pomatorhinus horsfieldii Sykes
  Muscicapinae Paradise flycatcher Terpsiphone paradisi L.,
    Redbreasted flycatcher Muscicapa ruficauda Swainson
    Verditer flycatcher Muscicapa thalassina Swainson
  Sylviinae Indian greatreed warbler Acrocephalus stentoreus (Hemprich & Ehrenberg)
  Turdinae Magpie-robin Copsychus saularis L.,
    Indian robin Saxicoloides fulicata L.,
    Blue chat Erithacus brunneus (Hodgson)
    Blue rock thrush Monticola solitarius L.,
    Malabar whistling thrush Myiophonus horsfieldii (Vigors)
    Orangeheaded ground thrush Zoothera citrina (Latham)
Paridae Parinae Yellowcheeked tit Parus xanthogenys Vigors
Sittidae Sittinae Velvetfronted nuthatch Sitta frontalis Swainson
Motacillidae   Forest wagtail Motacilla indica Gmelin
    Yellow wagtail Motacilla flava L.,
    Yellowheaded wagtail Motacilla citreola Pallas
    Grey wagtail Motacilla cinerea Tunstall
    White wagtail Motacilla alba L.,
    Large pied wagtail Motacilla maderaspatensis
Dicaeidae   Thickbilled flowerpecker Dicaeum agile (Tickell)
Nectariniidae   Purplerumped sunbird Nectarinia zeylonica L.,
    Small sunbird Nectarinia minima (Sykes)
    Purple sunbird Nectarinia asiatica (Latham)
Zosteropidae   White-eye Zosterops palpebrosus (Temminck)
Ploceidae Passerinae House sparrow Passer domesticus L.,
  Ploceinae Baya weaver bird Ploceus philippinus L.,
  Estrildinae Spotted munia Lonchura punctulata L.,
    Blackheaded munia Lonchura malacca L.,
    Whitebacked munia Lonchura striata L.,
* Endemic birds of the region

Mammals

Mammals are the group of animals that have reached a pinnacle during the evolution of life. In wildlife conservation, prioritisation is mainly given to mammals, because of their direct relevance to human beings. Their presence in the wild is an indication of the health of that habitat. The study area harbours many mammalian species as listed in Table 11. Of the 43 mammals recorded from the sanctuary, Tiger and Lion-tailed Macaque are endangered, and leopard is vulnerable. Table 11 also lists the bats (flying mammals) found in this region.  The endemic and endangered lion tailed macaque is sighted in the Karani area. Reports indicate their presence in Kogar, Gurta, Kodachadri and Sharavathi valley area. Now its population is on the decline due to the destruction and fragmentation of habitat and hunting for its skin and meat.

Tigers (Panthera tigris tigris) inhabit mostly in the evergreen and moist deciduous forests. According to forest department 7 leopard and 2 tigers were found in the sanctuary and its immediate surroundings (Figure 2.3). In the sanctuary area tiger was sighted near Shashichowka, Kogar, Karumane and Karani. Linganamakki catchment area has records of 4 leopards and 6 tigers.

Table 11: Mammals of SVWS

Common Name Scientific Name IUCN Status
Slow Loris Loris tardigradus Lr-nt
Bonnet Macaque Macaca radiata Lr-lc
Lion-tailed Macaque *Macaca silenus EN
Hanuman Langur Semnopithecus entellus  
Indian Jackal Canis aureus Lr-lc
Indian Fox Vulpes bengalensis Lr-nt
Wild Dog or Dhole *Cuon alpinus Lr-nt
Sloth Bear Melursus ursinus VU
Common Otter Lutra lutra NE
Jungle Cat Felis chaus Lr-nt
Fishing Cat Felis viverrina VU
Brown Palm Civet *Paradoxurus jerdoni VU
Small Indian Civet Viverricula indica Lr-nt
Common Indian Mongoose Herpestes edwardsi Lr-lc
Small Indian Mongoose Herpestes auropunctatus  
Three-striped Palm Squirrel Funambulus palmarum Lr-lc
Jungle striped Squirrel *Funambulus tristriatus Lr-nt
Indian Giant Squirrel *Ratufa indica VU
Common Giant Flying Squirrel Petaurista petaurista Lr-nt
Indian Porcupine Hystrix indica Lr-lc
Indian Pangolin Manis crassicaudata Lr-nt
Black-naped Hare Lepus nigricollis Lr-lc
Leopard Panthera pardus VU
Tiger Panthera tigris EN
Wild Boar Sus scrofa cristatus Lr-lc
Indian Spotted Chevrotain or Mouse Deer Tragulus meminna Lr-nt
Barking deer or The Muntjac Muntiacus muntjak Lr-lc
Spotted Deer or Chital Axis axis Lr-lc
Sambar Cervus unicolor Lr-lc
The Gaur or Indian Bison Bos gaurus VU
Fulvous fruit bat Rousettus leschnaulti Lr-lc
Black-bearded tomb bat Taphozous melanopogon Lr-nt
Pouch bearing bat Saccolaimus saccolaimus DD
Greater false vampire Megaderma derma  
Lesser false vampire Megaderma spasma DD
Blyth's horse-shoe bat Rhinolophus lepidus Lr-nt
Fulvous leaf-nosed bat Hipposideros fulvus Lr-nt
Kantor's leaf-nosed bat Hipposideros Sp.  
Schneider's leaf-nosed bat Hipposideros speoris Lr-nt
Kelaart's leaf-nosed bat Hipposideros lankadiva VU
Burmese whiskered bat Myotis montivagus DD
Least pipistrelle Pipistrellus tenuis Lr-lc
Kelaart's pipistrelle Pipistrellus ceylonicus Lr-lc
Note:   * Western Ghats endemic
VU – Vulnerable, EN – Endangered, LR-lc – Lower risk least concerned, LR-nt – Lower risk near threatened, NE - Not evaluated.

Wildlife census data in the Kogaru and Kargal range in 1997

Animals Kogaru range Kargal range
Block counting Line transect Block counting
Gaur 52 65 61
Spotted deer 68 30 36
Sambar 13 18 13
Wild Boar 42 60 64
Urial 7 3 4
Dhole   9 17
Langur 122 40 57
Sloth Bear 4    
Monkey 170 25 39
Red giant squirrel 64 14 7
Peacock 80 17 10
Indian Hare   6 3
Jungle fowl   10 16
Barking deer   5 3
Hornbill   6 2
Owl   2 2
Monitor lizard   4 4
Tiger   1  
Leopard 4 (male – 3, female – 1) 1 (male –1)  
Source: Tiger, Leopard and other wildlife census of 1997. Office of the Deputy Conservator of Forest, Shimoga Wildlife Division, Shimoga


Figure 2.3:  Tiger and leopard distribution in SVWS

Aquatic Ecosystem

Aquatic ecosystems contribute to a large proportion of the planet's biotic productivity as about 30% of the world's primary productivity comes from plants living in the ocean. These ecosystems also include riverbanks, wetlands located at lakeshores, the ocean shoreline, and any habitat where the soil or vegetation is submerged for some duration. These ecosystems have been subjected to various levels of stresses, due to unplanned developmental activities in the last century. Anthropogenic activities involving changes in land use ultimately affects the receiving water in that drainage. Activities include unplanned agricultural practices, unscientific usage of inorganic fertiliser, pesticides and herbicides applied to crops, silt washed away because of vegetation removal, or even due to atmospheric deposition, or disposal of solid and liquid wastes. The Linganamakki reservoir (in eastern part) and Talakalale reservoir (northern side) form a part of the lacustrine ecosystem in SVWS, while many first and second order streams of river Sharavathi and Venkatapura forms the lotic ecosystem in the sanctuary.

Phytoplankton

Phytoplankton are the microscopic suspended algae that occur in different forms such as unicellular, colonial or filamentous, which are mainly photosynthetic in nature. They are one of the most rapid detectors of environmental change and are regarded as the primary producers in aquatic food chain. The family, genus and species composition of phytoplankton is listed in Table 12.1. Species list is given in Table 12.2

Table 12.1: Familywise composition of phytoplankton.

Family composition I-collection II-collection III -collection
Desmidials 50 51 48
Bacillariophyceae 12 25 22
Cyanophyceae 4 6 6
Chlorococcales 3 9 8
Dinophyceae 2 2 4
Chrysophyceae   1 4
Total no. of genera 44 64 61
Total no. of species 71 94 92

Qualitative dominance of the phytoplankton was in the order of Desmidials > Bacillariophyceae > Cyanophyceae >Chlorococcales > Dinophyceae in the first sampling. In this collection population of Desmidial member Staurastrum multispiniceps was highest (58,944/L) in Muppane of the reservoir. While, in the second sampling, qualitative dominance was in the order of Desmidials > Bacillariophyceae > Chlorococcales > Cyanophyceae > Dinophyceae >Chrysophyceae. Similarly in the third collection, it was in the order of Desmidials > Bacillariophyceae > Chlorococcales > Cyanophyceae > Dinophyceae = Chrysophyceae.  Table 12.3 reveals diversity and diversity indices calculated in various sampling localities.

Table 12.2: Phytoplankton species in SVWS

I. Muppane
Bacillariophyceae (Diatoms) Collections
I II III
Cymbella chandolensis Gandhi   +  
Gyrosigma attenuatum (Kuetz.) Rabh.   +  
Melosira islandica O. Muell v. helvetica O. Muell   + +
M. granulata (Ehr.) Ralfs. v. mazzanensis Meister     +
Navicula pygmaea Kuetz. v. indica Skv +    
N.viridula Kuetz. V. capitata Mayer   + +
Nitzschia philippinarum Hustedt +    
Pinnularia streptoraphe Cleve     +
Synedra ulna (Nitz.) Ehr. v. danica Kuetz. Grun.     +
Desmidials
Arthrodesmus curvatus Turn +    
A. psilosporus (Nodrdst. & Lofg.) De Toni Formae +   +
Cosmarium contractum Kirchn   + +
C. ordinatum (Borges) West & West var.borgei Scott Gronbl. +    
C. lundellii Delp var circulare (Reinch) Krieg +    
C. spinuliferum West & West     +
Desmidium baileyi (Ralfs) Nordst fa.longiprocessum +    
D. baileyi (Ralfs) Nordst fa. tetragonum Nordst   +  
Euastrum gnathophorum West & West     +
Spondylosium planum (Wolle.) West & West +    
Staurastrum cerastes Scott.& Presc. +    
S. euprepes +    
S. freemanii West & West var.nudiceps Scott & Presc. + + +
S. limneticum Schm. Var. burmense West & West + + +
S. multispiniceps +   +
S. peristephes   + +
S. prionotum   + +
S. sexangulare Lund var.productum Nordst +    
S. tauphorum West & West +    
S. thienemannii Krieg     +
S. tohopekaligense Wolle var. insigne West & West Formae +   +
Triploceros gracile Bail fa. curvatum + + +
T. gracile Bail fa. undulatum Scott & Presc.     +
Xanthedium hastiferum Turn. Var. javanicum (Nordst.) Turn. fa. Planum Turn      
X. perissacanthum Scott. & Presc. Var. minus. + +  
Chlorococcales
Ankistrodeimus falcatus (Corda) Ralfs +   +
Cyanophyceae
Aphanocapsa rivularis (Carm) Rabenhorst     +
Chroococcus limneticus var.elegans G. M. Smith +    
Microcystis aeruginosa Kuetz, emend, Elenkin   +  
Dinophyceae
Ceratium hirundinella (O.F. Muell) Dujardin +    
Chrysophyceae
Dinobryon sertularia Ehrberg.      

 

II. Talakalale
Bacillariophyceae (Diatoms) Collections
I II III
Cymbella powaiana Gandhi     +
Gomphonema longiceps Ehr. v. subclavata Grun   + +
Melosira islandica O. Muell v. helvetica O. Muell   + +
Navicula cari Ehr.   +  
N.viridula Kuetz. V. capitata Mayer   +  
Pinnularia maharashtrensis     +
Synedra ulna (Nitz.) Ehr. v. danica Kuetz. Grun.   +  
Desmidials
Arthodesmus psilosporus (Nodrdst. & Lofg.) De Toni Formae +   +
Cosmarium contractum Kirchn   + +
C. subturgidum (Turn.) Schm. Fa. minus Schm   +  
Desmidium baileyi (Ralfs) Nordst +    
D. baileyi (Ralfs) Nordst fa. tetragonum Nordst   +  
Euastrum gnathophorum West & West   + +
Spondylosium planum (Wolle.) West & West +    
Staurastrum freemanii West & West var.nudiceps Scott & Presc. + + +
S. limneticum Schm. Var. burmense West & West + +  
S. longibrachiatum (Borge) Gutz. +    
S. multispiniceps. +    
S. peristephes + + +
S. prionotum   + +
S. sexangulare Lund var.productum Nordst +    
S. rosei Playf. var. stemmatum     +
S. thienemannii Krieg fa. triradiatum     +
Triploceros gracile Bail fa. curvatum   +  
X. perissacanthum Scott. & Presc. Var. minus. +    
Chlorococcales
Ankistrodeimus falcatus (Corda) Ralfs     +
Eudorina elegans Ehrenberg +    
Scenedesmus acuminatus (Lag) Chodat     +
S. dimorphus (Turp.) Kuetzing   +  
S. opoliensis var contacta Prescott     +
Cyanophyceae
Aphanocapsa rivularis (Carm) Rabenhorst   +  
Chroococcus limneticus var.elegans G. M. Smith +    
Coelosphaerium dubium Grunow     +
Dinophyceae
Ceratium hirundinella (O.F. Muell) Dujardin + + +

 

III. Reservoir centre
Bacillariophyceae (Diatoms) Collections
I II III
Cymbella ventricosa Kuetz.   +  
Gomphonema lanceolatum Her   +  
G. longiceps Ehr. v. subclavata Grun +   +
Gyrosigma attenuatum (Kuetz.) Rabh.   +  
Melosira islandica O. Muell v. helvetica O. Muell   + +
Navicula cari Ehr.     +
N.viridula Kuetz. V. capitata Mayer   + +
N. subdapaliformis Gandhi +    
Pinnularia lundii Hustedt     +
Desmidials
Arthodesmus psilosporus (Nodrdst. & Lofg.) De Toni Formae   + +
Cosmarium contractum Kirchn   +  
C. margaritatum (Lund) Roy & Biss var sublatum (Nordst.) Krieg   +  
C. scabrum Turn   +  
Desmidium baileyi (Ralfs) Nordst fa.longiprocessum +    
Euastrum ansatum Ehr. v. Triporum +    
E. gnathophorum West & West var.bulbosum   + +
Pleurotaenium ehrenbergi (Breb.) De Bary v. undulatum Schaarschm     +
Spondylosium planum (Wolle.) West & West +    
Staurastrum cerates Lund var pulchrum Scott & Gronbl. fa   +  
S. freemanii West & West var.nudiceps Scott & Presc. + + +
S. limneticum Schm. Var. burmense West & West + +  
S. longibrachiatum (Borge) Gutz. +    
S. multispiniceps +    
S. peristephes + +  
S. prionotum   + +
S. sexangulare Lund var.productum Nordst +    
S. thienemannii Krieg fa. triradiatum   +  
X. perissacanthum Scott. & Presc. Var. minus. +    
Chlorococcales
Ankistrodeimus falcatus (Corda) Ralfs     +
Pediastrum simplex Meyen   +  
Scenedesmus acuminatus (Lag) Chodat     +
Cyanophyceae
Chroococcus limneticus var.elegans G. M. Smith +    
C. turgidus (kuetz.) Naegeli   +  
Microcystis aeruginosa Kuetz, emend, Elenkin   + +
Dinophyceae
Ceratium hirundinella (O.F. Muell) Dujardin     +

 

IV. Yennehole
Bacillariophyceae (Diatoms) Collections
I II III
Eunotia praerupta Ehr. + +  
Gomphonema gracile Ehr. v. intricatiforme Mayer +    
G.lanceolatum Her   +  
Melosira islandica O. Muell v. helvetica O. Muell     +
M. granulata (Ehr.) Ralfs. v. mazzanensis Meister     +
Navicula cuspidata Kuetz.f.brevirostrata Gandhi +    
N. laeta A. Mayer +    
N. viridula Kuetz. +    
Nitzschia closterium W. Smith +    
N. obtusa W. Smith v. scalpelliformis Grun +    
Pinnularia gracioloides Hustedt     +
Synedra acus Kuetz. +    
Desmidials
Arthrodesmus constrictus G. M Smith var.longispinus Gronbl.   + +
A.curvatus Turn.var.latus +    
Closterium ehrenbergii Menegh   +  
C. porrectum Nordst +    
C. ralfsii Breb var.hybridrum Rab   +  
Cosmarium askenasyi Schm.fa.latum Scott & Presc     +
C. contractum Kirchn   +  
C. decoratum West & West     +
C. pseudoconnatum Nordst +    
C. punctulatum Breb.var.sub punctulatum (Nordst.) Borges +    
Desmidium baileyi (Ralfs) Nordst fa.longiprocessum   +  
D. bengalicum Turn +    
D. quadratum Nordst   +  
Euastrum gnathophorum West & West var.bulbosum   +  
E. sinuosum Lenorm. var. parallelum Krieg +    
Gonatozygon aculeatum Hastings   + +
Hyalotheca dissiliens (Smith) Breb. var. hains Wolle +    
Micrasterias foliacea Bail var. quadrinflata   +  
M. mahabuleshwarensis Hobs.var.chauliodon +    
M. quadridentata (Nordst.) Gronbl.fa, indonesinsis     +
Staurastrum anceps Her.   +  
S. anceps Ehr. v. hyalina Brun. et.Perag     +
S. freemanii West & West var.nudiceps Scott & Presc. +   +
S. limneticum Schm. Var. burmense West & West +   +
S. multispiniceps +    
S. peristephes   +  
S. sebaldi Reinsch var.ornatum Nordst     +
S. tohopekaligense Wolle var. trifurcatum West & West +    
S. wildmanii Gutw.   +  
Chlorococcales
Ankistrodeimus falcatus (Corda) Ralfs +   +
A. spiralis (Turner) Lemmermann +    
Gomphosphaeria aponina var. delicatula virieux   +  
Kirchnerilla lunaris (Krich.) Moebius +    
Muogeotia punctata Wittrock   +  
Pediastrum simplex Meyen     +
Scenedesmus bijuga (Turp.) Lagerheim   +  
Cyanophyceae
Microcystis aeruginosa Kuetz, emend, Elenkin + + +
Gomphosphaeria aponina var. cordiformis Wolle     +
Dinophyceae
Ceratium hirundinella (O.F. Muell) Dujardin     +
Chrysophyceae
Dinobryon calciformis Bachmann     +
D. divergens Imhof   +  
D. sertularia Ehrbg.     +

 

V. Madenur
Bacillariophyceae (Diatoms) Collections
I II III
Cymbella laevis Naeg   +  
C. ventricosa Kuetz.   +  
Gomphonema lanceolatum Her   +  
G. longiceps Ehr. v. subclavata Grun   + +
Gyrosigma attenuatum (Kuetz.) Rabh.(Nordst & Lofg.) De Toni   +  
Melosira granulata (Ehr.) Ralfs. v. mazzanensis Meister     +
M. islandica O. Muell v. helvetica O. Muell   + +
Navicula viridula Kuetz. V. capitata Mayer   + +
Nitzschia obtusa W. Smith v. scalpelliformis Grun   +  
N. radiosa Kuetz.   +  
Desmidials
Arthodesmus psilosporus (Nodrdst. & Lofg.) De Toni Formae   + +
Cosmarium contractum Kirchn     +
Desmidium bengalicum Turn fa.quadratum   +  
Euastrum gnathophorum West & West var.bulbosum   + +
Onychonema laeve Nordst. var. latum West & West     +
Staurastrum cerates Lund var pulchrum Scott & Gronbl. fa   +  
S. emaciatum   +  
S. freemanii West & West var.nudiceps Scott & Presc.   + +
S. gralile Ralfs fa. Kriegeri     +
S. limneticum Schm. Var. burmense West & West   + +
S. multispiniceps   +  
S. prionotum   + +
S. tohopekaligense Wolle var. insigne West & West Formae   +  
S. sebaldi Reinsch var.ventriverrucosum     +
Triploceros gracile Bail fa. undulatum Scott & Presc.     +
Xanthedium perissacanthum Scott. & Presc. Var. minus.   +  
Chlorococcales
Muogeotia punctata Wittrock   +  
Spirogyra rhizobrachialis Jao   + +
Cyanophyceae
Chroococcus turgidus (kuetz.) Naegeli   +  
Gomphosphaeria lacustris Chodat     +
Microcystis aeruginosa Kuetz, emend, Elenkin   +  
Dinophyceae
Ceratium hirundinella (O.F. Muell) Dujardin     +
Chrysophyceae
Dinobryon calciformis Brachmann     +

Table 12.3:  Diversity indices at various sampling localities.

Parameter Collection Muppane Talakalale Reservoir Centre Yenne holé Madenur
Total individual 1 10339 2770 3414 820 -
2 49 96 33 437 74
3 232 59 88 585 175
Total species 1 21 13 14 23 -
2 15 18 18 19 24
3 21 17 15 20 19
Species richness 1 2.16 1.51 1.59 3.27 -
2 3.59 3.72 4.86 2.96 5.34
3 3.67 3.92 3.12 2.98 3.48
Shannon-diversity 1 1.96 1.85 2.24 2.69 -
2 2.43 2.11 2.75 1.97 2.85
3 1.57 2.45 2.21 1.57 2.21
Simpson-dominance 1 0.2 0.22 0.12 0.09 -
2 0.11 0.23 0.07 0.24 0.07
3 0.4 0.12 0.14 0.38 0.15
Simpson-diversity 1 0.79 0.77 0.87 0.9 -
2 0.88 0.76 0.92 0.75 0.92
3 0.59 0.87 0.85 0.61 0.84

Abrupt variations in total number of individuals indicate that the growth and distribution patterns of phytoplankton are not uniform. High total number of individuals during I-collection compared to other two can be attributed to the rains during the month of September just prior to I-collection during October, which might have added nutrients to the waters along with run-off water from the catchment.

In order to apply biological means of determining the trophic status, Shannon and Weiner’s species diversity values were calculated. The degrees of pollution is categorized based on the ranges of Shannon and Wiener’s species diversity as ‘slight’ (species diversity range of 3.0 – 4.5), ‘light’ (2.0 – 3.0), ‘moderate’ (1.0 – 2.0) and ‘heavy’ (0.0 – 1.0).

From Table 12.3  it is clear that in general, species diversity values are in the range of moderate or light pollution level. From Shannon’s diversity indices it is clear that the waters of sanctuary area are of oligotrophic nature.

A total of 109 species are collected from the SVWS; 28 species of diatoms, 58 species of desmidials, 12 species of chlorococales, 7 species of cynophyceae, 3 species of chrysophyceae and a species of dinophyceae represent total number. The biological examination of the stream and reservoir ecosystems showed a rich and diverse phytoplankton population. Desmids predominated in reservoir waters while diatoms in streams.

Zooplankton

Zooplankton are the primary consumers of an aquatic ecosystem, which feed on phytoplankton. Rotifera, Cladocera and Copepoda are the major groups among freshwater zooplankton. A detailed knowledge about zooplankton composition and their seasonal fluctuations is essential for proper management of water bodies. To study the zooplankton diversity in aquatic systems of the SVWS water samples were collected at Muppane, Talakalale, Reservoir center and Yenneholé. Majority of rotifers inhabits freshwater but some genera also occur in brackish water and marine environment. Most species are free-living while some are epizoic or parasitic. Generally the size of the rotifera range from 400 µm to 0.2 mm. Six species belonging to two families are recorded in the present study. Number of species belonging to rotifers, cladocerons and copepoda are given in Table 12.4.

Table 12.4: Zooplankton of SVWS

Groups Family Muppane Talakalale Reservoir
Centre
Yenneholé
Rotifera Brachionidae 1 0 1 1
Lecanidae 1 2 1 3
Cladocera Sididae 1 0 0 0
Daphnidae 1 1 0 0
Moinidae 1 0 1 0
Macrothricidae 0 0 0 1
Chydoridae 1 0 0 1
Copepoda Cyclopidae 0 0 0 1
Diaptomidae 1 1 1 0

Cladocerans are ubiquitous in distribution, i.e., they are found in the Arctic to Antarctic, in temperate and tropical latitudes. Recently they were also reported from ground water (Dumont, 1987; Negrea 1983). The size ranges from 0.2 mm to 18 mm. Like other Zooplankton cladocerans are excellent food for zooplanktivorous fish. Six species belonging to five families are recorded in the present study (Table 12.4).  Copepods are the very ancient arthropods. In inland waters copepods are well known, up to family level, but numerous species are yet to be discovered. Of the three groups of zooplankton, Copepoda was least represented in terms of diversity with only three species (Table 12.4).

In the present study, 15 species of zooplankton were recorded from four localities along the River Sharavathi, showing a typical tropical assemblage. Table 12.5 lists locality-wise species list. Large zooplankton species were absent in this river system, probably due to high predatory pressure.

Table 12.5: Zooplankton diversity in SVWS

Rotifers
Species Sites
1 2 3 4
Family: Brachionidae
Brachionus quadridentatus Hemann, 1783     +  
B. falcatus (Zacharias, 1898) +      
Keratella tropica (Apsein, 1907)       +
Family: Lecanidae
Lecane bulla (gosse, 1888). + + + +
L. lateralis sharma, 1978.       +
Lecane sp.   +   +

Cladocerans
Species Sites
1 2 3 4
Family:Sididae
Diaphanosoma sarsi Richard, 1895 +      
Family: Daphniidae
Ceriodaphnia cornuta Sars, 1885 + +    
Family: Moinidae
Moina micrura Kurz, 1874   +   +  
Family: Macrothricidae
M. odiosa (Gurney, 1907)       +
Family: Chydoridae, Sub-family: Chydorinae
Ephimeroporus barrosi (Richard, 1894) +      
Sub-family: Aloninae
Alona verrucosa (Sars, 1901)       +

Copepodans
Species Sites
1 2 3 4
Family: CyclopidaeSub-family: Cyclopinae
Microcyclops varicans Sars, 1863       +
Family: Diaptomidae
Heliodiptomus cinctus (Gurney, 1907)     +  
Allodiaptomus mirabilipes (Kiefer, 1936) + +    

Ichthyofauna

The Western Ghats records 288 species belonging to 12 orders, 41 families and 109 genera, of which 118 species are endemic and 51 are unique. This diverse fish fauna composition aptly demonstrates the hotspots status of the Western Ghats. A major portion of the Linganamakki reservoir falls under the SVWS. The ichthyological studies gain importance, as it helps to adopt appropriate conservation strategies for sustainable management of the aquatic ecosystem. Several rivers in the Western Ghats are being exploited for fisheries and there is hardly any information available on its effect on such a pristine resource stock of the region. This necessitates a detailed investigation on fish and fisheries.

We have recored from SVWS 60 species of fishes (Table 13.1). Considering the IUCN status of these species, there are about 16.6% (10 species) endangered, 18.3% (11 species) vulnerable, 16.6% (10 species) data deficient, 33.2% (20 species) are with lower risk and the status of 3 species is unknown. There is about 16 endemic fish species in the reservoir. Compared to the Western Ghats this value is relatively low, which could be attributed to the formation of the reservoir that has lead to the flourishing of generalist species and diminishing of sensitive endemic species. Also, the introduction of the exotic species into the reservoir has increased the species richness while decreasing the endemism. About 16.6% (10 species) are restricted to peninsular India and 41.6% (25 species) have their distribution all over India.

Table 13.1: Fish species in SVWS

Family Species Distribution IUCN status
Bagridae Batasio sharavatiensis Endemic to Sharavathi DD
Bagridae Mystus malabaricus Endemic to Western Ghats EN
Balitoridae Nemacheilus anguilla Endemic to Western Ghats LR
Balitoridae Schistura semiarmatus Endemic to Western Ghats VU
Cyprinidae Barilius bakeri Endemic to Western Ghats VU
Cyprinidae Barilius canarensis Endemic to Western Ghats DD
Cyprinidae Barilius gatensis Endemic to Western Ghats DD
Cyprinidae Garra gotyla stenorhynchus Endemic to Western Ghats EN
Cyprinidae Gonoproktopterus dubius? Endemic to Western Ghats EN
Cyprinidae Gonoproktopterus kolus Endemic to Western Ghats EN
Cyprinidae Labeo kontius Endemic to Western Ghats LR
Cyprinidae Osteocheilichthys nashii Endemic to Western Ghats VU
Cyprinidae Puntius arulius Endemic to Western Ghats EN
Cyprinidae Puntius sahyadriensis Endemic to Western Ghats DD
Cyprinidae Salmostoma boopis Endemic to Western Ghats LR
Sisoridae Glyptothorax lonah Endemic to Western Ghats LR
Cichlidae Oreochromis mossambica Exotic  
Bagridae Mystus bleekeri India VU
Bagridae Mystus cavesius India LR
Balitoridae Acanthocobitis botia India LR
Belonidae Xenentodon cancilla India LR
Chandidae Chanda nama India VU
Chandidae Parambassis ranga India DD
Channidae Channa marulius India LR
Channidae Channa orientalis India VU
Claridae Clarias batrachus India VU
Cyprinidae Amblypharyngodon mola India LR
Cyprinidae Barilius bendelisis India LR
Cyprinidae Oreichthys cosuatis India DD
Cyprinidae Puntius chola India VU
Cyprinidae Puntius sophore India LR
Cyprinidae Puntius ticto India LR
Cyprinidae Rasbora daniconius India LR
Cyprinidae Tor mussullah India EN
Gobidae Glossogobius giuris India LR
Mastacembelidae Mastacembelus armatus India LR
Schilbeidae Pseudeutropius atherinoides India EN
Siluridae Ompok bimaculatus India EN
Siluridae Ompok pabo? India DD
Siluridae Wallago attu India EN
Cyprinidae Brachydanio rerio India LR
Claridae Clarias dussumieri India VU
Aplocheilidae Aplocheilus lineatus Southern India LR
Bagridae Mystus keletius Southern India DD
Balitoridae Schistura denisonii densisonii Southern India VU
Belontidae Pseudophromenus cupanus Southern India DD
Cobitinae Lepidocephalus thermalis Southern India LR
Cyprinidae Cirrhinus fulungee Southern India LR
Cyprinidae Danio aequipinnatus Southern India LR
Cyprinidae Puntius fasciatus Southern India EN
Cyprinidae Puntius filamentosus Southern India DD
Cyprinidae Tor khudree Southern India VU
Balitoridae Schistura sp.    
Balitoridae Schistura sp.    
Cyprinidae Catla catla introduced  
Cyprinidae Cirhinus mrigala introduced  
Cyprinidae Cyprinus carpio communis Exotic  
Cyprinidae Cyprinus carpio Exotic  
Cyprinidae Cyprinus carpio specularis Exotic  
Cyprinidae Labeo rohita introduced  

Large-scale fishery began in this reservoir with the commissioning of the dam. This commercialisation of inland fishery that took place over a few decades has led to transformation of the subsistence fishing into commercial fishing in the wildlife sanctuary area of the Linganamakki reservoir. The introduction of exotic and alien species in to the Linganamakki reservoir has been practiced since 1965. Fingerlings of Catla catla, Labeo rohita, Cirhina mrigala, Cyprinus carpio and Oreochromis mossambica are introduced haphazardly into the reservoir on yearly basis.

The commercial fish catch of the reservoir is dominated by species belonging to Cyprinidae (54%). The other major families are Bagridae (23%) and the Siluridae (15%). When biomass is considered, the fast growing Indo-gangetic carps, popularly known as Indian major carps, occupy a prominent place namely Catla catla (21%), Labeo rohita (8.4%) and Cirhina mrigala (6.32%). These fishes are introduced to fulfill the commercial fish requirement along with the exotic species (Cyprinus carpio 21%). The native fishes with significant biomass are Gonoproktopterus kolus (11.5%), Ompok bimaculatus (10%) and Wallago attu (9%).

Data on fish catch of the selected five localities (Table 13.2) show that at the center of the reservoir (Holebagilu), the yield variation is very high compared to other regions. During monsoon season, the central region yields the introduced species in bulk. In the peripheral localities (Muppane, Konjavalli, Melmanji and Kogar) variation in catch during two seasons is less.

Table 13.2: Fish-catch observed at different locations during the year 2003-04

Locality Catch per unit effort (Kg/boat/day)
Non-monsoon Monsoon
Holebagilu 1.34 39.4
Muppane 7.93 16.5
Konjavalli 6.2 16.5
Melmanji 6.8 24.2
Kogar 8.2 28.5

The fish biomass composition (Table 13.3) in the central region is dominated by introduced species (Holebagilu - 55.8%) during monsoon season. Among the indigenous population, Ompok bimaculatus has shown significant biomass in these localities. Whereas in other localities without any introduced species, their catch includes indigenous commercial fishes like Gonoproktopterus kolus, Wallago attu, Mastacembelus armatus and Ompok bimaculatus. Apart from G. kolus, the market value for all indigenous fishes is higher than the introduced species.

Table 13.3: Percentage catch composition of various species during monsoon season

Species name

Percentage biomass

Holebagilu

Muppane

Konjavalli

Melmanji

Kogar

Catla catla

25.4

0.0

0.0

0.0

0.0

Cyprinus carpio

12.7

0.0

0.0

0.0

0.0

Labeo rohita

10.1

0.0

0.0

0.0

0.0

Cirhina mrigala

7.6

0.0

0.0

0.0

0.0

Cirhinus fulungee

0.0

12.7

5.4

2.5

3.2

Gonoproktopterus kolus

0.0

39.0

43.4

38.9

43.2

Mastacembelus armatus

8.1

9.7

12.1

4.9

8.4

Mystus bleekeri

0.0

0.3

0.0

0.0

0.0

Mystus cavacius

9.1

7.2

1.4

0.6

0.5

Mystus malabaricus

1.7

2.7

1.4

0.6

2.1

Ompok bimaculatus

24.0

23.9

15.9

8.1

37.1

Ompok pabo

0.0

1.3

2.6

0.9

1.5

Osteocheilichthys nashii

0.0

0.9

0.0

0.0

0.0

Pseudeutropius atherinoides

0.0

0.2

0.3

0.1

0.2

Puntius filamentosus

0.0

1.1

1.4

1.5

3.8

Tor khudree

0.0

0.9

0.0

0.0

0.0

Tor mussullah

0.0

0.0

0.9

0.6

0.0

Wallago attu

0.0

0.0

15.1

41.2

0.0

Xenentodon cancilla

1.2

0.0

0.0

0.0

0.0

During summer season, catch is mainly represented by Mystus cavecius, M. malabaricus and Mastacembelus armatus in almost all the localities (Table 13.4). This shows the absence of any introduced species in these localities. At the peripheral localities Gonoproktopterus kolus shows significant catch whereas its catch is negligible at the central region.

Table 13.4:  Percentage catch composition of various species during non-monsoon season

Species name Percentage biomass
Holebagilu Muppane Konjavalli Melmanji Kogar
Native          
Gonoproktopterus kolus 0.0 28.4 28.9 13.3 11.0
Cirhina fulungee 5.6 8.5 8.4 2.2 4.6
Garra gotyla stenorhynchus 0.0 1.5 0.6 0.0 0.0
Mastacembelus armatus 0.0 25.2 19.3 17.8 19.5
Mystus cavecius 16.8 3.8 6.0 8.9 14.6
Mystus malabaricus 22.4 5.7 7.2 7.8 10.1
Ompok bimaculatus 32.8 8.3 14.1 39.1 29.5
Ompok pabo 0.0 13.9 10.6 9.8 10.7
Oreochromis mossambica 0.0 1.0 2.4 1.1 0.0
Puntius arulius 0.1 0.0 0.0 0.0 0.0
Puntius filamentosus 17.9 0.0 0.0 0.0 0.0
Tor khudree 0.0 3.8 2.4 0.0 0.0
Xenentodon cancilla 4.5 0.0 0.0 0.0 0.0

The fish catch composition shows variations between different sites as the composition in the peripheral regions of the sanctuary like Holebagilu is of introduced species while Yenneholé tributary is of native species.

Fishery in the sanctuary is being practiced illegally and continued overharvesting proves to be unsustainable. Yenneholé tributary has witnessed a self-preserving fishery within the biological limits of its resource’s productivity, through a limited seasonal uptake, while ensuring future harvests. On the other hand, Holebagilu region, which supplies the fish requirements of the nearby urban centers has large number of fishermen and wider access and has led to illegal fishing activities.

The fortunes of the fishermen at the central parts of the reservoir like Holebagilu and the Hasaramakki seem to have touched bottom during recent years. During the winter and the summer seasons, the catch kg/per person/day is around one, which fetches about 25 rupees. During monsoon season, they get the introduced species. The competition for food and space between the exotic and indigenous has also led to the decline in the latter.

Variable fishing pressure: Monsoon is the peak fishing period with 3.4 times fish catch per person per day compared to non-monsoon period and accounts for 86.7% of the total fish-catch. Increased fishing pressure is noticed with migratory fishermen (accounting to 63% of the total) from various parts of peninsular India and the density of fishermen increases to 2.75 times the native fisher folk.  During the initial monsoon season, the reservoir attains the minimum water spread area. It is observed that most of the fishermen get concentrated in the central regions like Holebagilu leading to overexploitation of fish resource.

Muppane, Konjavalli, Melmanji and Kogar represent the peripheral localities of the western region. The biomass composition of this region shows that in these localities, the catch is formed by the native species. These are the flood plains where majority of the fish species breed during monsoon season. Huge quantities of fish catch in these localities during monsoon season poses severe threat to their population. It is evident that the catch per unit effort increases at the periphery than the other localities.

Fish translocation from other basins: Details on the pattern of introduction clearly reveal that no scientific approach has been adopted before determining the quantity of introduction. Seeds have been introduced depending on the availability. This unscientific approach has resulted in an artificial system of fishing wherein the indigenous fishing population has to rely on an external source to increase the fishing stock. The low catches during non-monsoon season affect the permanent fishermen of the region who are completely dependent on fish resources for livelihood. The biomass composition of this region also reveals that other than catfishes, no other native species has succeeded to form a stable population. Thus the fishermen are dependent on an artificial system in the form of introduction and harvest. It is implicative that the original fauna has been changed and hardy fish species has taken advantage of the vacant niches. Thus translocation of fishes from other basins has led to changes in the species composition.

Amphibians

Amphibians are the best ecological indicators among vertebrates for the unique features like duplex life style, moist permeable skin and ectothermic nature. They are the indicators of habitat fragmentation, as they negatively respond to both qualitative and quantitative changes in the habitat, ecosystem stress, impact of anthropogenic activities like dam construction, and sedimentation in streams due to road construction.

Twenty-four species of amphibians with 178 individuals were recorded in SVWS  accounting to 19% of the Western Ghats. Of the 24 species, 16 are endemic (71%) to the Western Ghats. Based on the IUCN criteria for conservation priority, 1 species endangered (Nyctibatrachus aliciae), 2 vulnerable, 2 threatened, 14 with least concern and 5 data deficient. These species belong to four families, namely bufonidae, microhylidae, ranidae and ichthyophiidae. Ranidae members predominate in the richness, abundance and endemism (20, 168, and 15). Based on the species abundance (Figure 2.4), the top six species include Euphlyctis cyanophlyctis (43)followed by Philautus cf. leucorhinus (24), Nyctibatrachus aliciae (21), Indirana semipalmata (16), Micrixalus saxicola (11) and Rana temporalis (10).Presence of endemics (16 amphibian species), endangered species Nyctibatrachus aliciae and vulnerable species Micrixalus saxicola and Nyctibatrachus major indicates the ecological importance of the region. Species list is provided in Table 13.5.

Table 13.5: Amphibians of Sharavathi Valley Wildlife Sanctuary

Species Endemism IUCN status
Bufonidae
Bufo melanostictus NE LC
Bufo scaber NE LC
Microhylidae
Microhyla ornata NE LC
Ranidae
Euphlyctis cyanophlyctis NE LC
Fejervarya keralensis E LC
Fejervarya limnocharis NE LC
Fejervarya rufescens E LC
Hoplobatrachus tigerinus NE LC
Indirana beddomii E LC
Indirana semipalmata E LC
Micrixalus saxicola E VU
Nyctibatrachus aliciae E EN
Nyctibatrachus major E VU
Philautus cf. leucorhinus E DD
Philautus cf. luteolus E DD
Philautus cf. ponmudi E DD
Philautus tuberohumerus E DD
Polypedates cf. leucomystax NE LC
Rana curtipes E LC
Rana malabarica NE LC
Rana temporalis E NT
Rana sp. E DD
Rhacophorus malabaricus E LC
Ichthyophiidae
Ichthyophis beddomei E LC
Note:   E – Endemic to Western Ghats; NE – Non-endemic to Western Ghats; EN- Endangered; Vu – vulnerable; NT–Near threatened; LC – Least concerned; DD – data deficient.

Nair and Gadgil (1975) reported the elephants during 1960s in SVWS. Over the period the elephants have disappeared from the park. Similarly from the north of the sanctuary i.e. between Sharavathi and Aghanashini rivers also the elephants have disappeared in recent years (Kumara and Singh 2005b). The probable reasons could be developmental activities like dam, road and increased number of human enclaves, made them completely isolation from the main population, and probably resulted in biased sex ratios over a period and in turn on breeding efficiency. Further, gradual elimination of the individuals drove into local extinction.


Figure 2.4: Amphibian species abundance in SVWS

An assessment of the Ecological status of Sharavathi Valley Wildlife Sanctuary (Sameer Ali et.al 2007) carried outthrough the estimation of species composition and their relative abundance with reference to space and time in a region. Faunal studies indicate the diverse groups of organisms found in the sanctuary. The data gathered both by sampling and opportunistic surveys are listed in Table 14.1.

Table 14.1: Faunal composition in Sharavathi Valley Wildlife Sanctuary

Fauna Species
Ants 84
Coleopterans 166
Butterflies 173
Molluscs 21
Amphibians 24
Fishes 60
Birds 122
Reptiles 23
Mammals (including Bats) 43

Kumara H.N. 2007 studied the mammals of Sharavathi wildlife Sanctuary. A total of 1,332 animals belongs to ten species were sighted in 550 encounters during the day walk (Table 14.2). The ten species includes four arboreal mammals and six terrestrial mammals, and the relative abundance of arboreal mammals (7.19 +0.471) was more than (z= 14.64, p< .000) the terrestrial mammals (0.24 +0.056).  A total of 50 animals belonging to eight species including two unidentified small carnivores were sighted during the night walk (Table 14.3), which provides an overall relative abundance of 0.87 animals per kilometre. However the relative abundance of arboreal mammals (0.59) was higher than the small carnivores (0.22) and the other mammals include chevrotain and porcupine Hystrix indica (0.06), among arboreal mammals the slender loris (0.35) was more than the giant flying squirrel (0.23) and Travancore flying squirrel (0.01).

Table 14.2:  Relative abundance of mammals in the Sharavathi Valley Wildlife Sanctuary

Species No. of sightings Total no. ofanimals sighted during the day No. animals seen/km (SE)
Arboreal mammals   
Hanuman langur 243 835 4.52 (+0.380)
Bonnet macaque 31 147 0.91 (+0.241)
Lion-tailed macaque 7 23 0.12 (+0.057)
Indian giant squirrel 238 287 1.54 (+0.117)
Total 519 1292 7.19 (+0.471)
Terrestrial mammals
Gaur 1 1 0.004 (+0.004)
Sambar 9 13 0.05 (+0.020)
Spotted deer 4 6 0.05 (+0.026)
Indian muntjac 15 17 0.11 (+0.030)
Wild pig 1 2 0.01 (+0.012)
Indian grey mongoose 1 1 0.005 (+0.005)
Total      

Table 14.3: Relative abundance of mammals in Sharavathi Valley Wildlife Sanctuary

Species No. animals seen during the night No. animals seen/km
Small carnivores
Leopard cat 5 0.07
Asian palm civet 3 0.04
Brown palm civet 5 0.07
Unidentified small carnivores 2 0.03
Total 15 0.22
Arboreal mammals
Slender loris 24 0.35
Giant flying squirrel 16 0.23
Travancore flying squirrel 1 0.01
Total 41 0.59
Other mammals
Indian spotted chevrotain 3 0.04
Indian crested porcupine 1 0.01
Total 4 0.06
Grand Total 60 0.87

Among various anthropogenic impacts, impounding of waters for electricity generation seems to have significantly altered terrestrial as well as aquatic ecosystems and associated biota including fish fauna. In this regard, a study was conducted in Sharavathi River of central Western Ghats to understand fish species composition with respect to landscape dynamics. Of the 64 fish species recorded, 25 were exclusive to the tributary streams, 29 to the reservoir and 10 common to both. Among these, 18 species were endemic to the Western Ghats and 10 to peninsular India. The study, carried out using a combination of remote sensing data as well as field investigations, shows that the streams having their catchments covered with evergreen to semi-evergreen forests, having high levels of ever greenness and endemic tree species of Western Ghats, were also richer in fish diversity and endemism compared to those catchments with other kinds of vegetation. It also highlights that endangered and endemic fish species are precariously clinging onto the stream habitats where patches of primeval forests, though degraded substantially, are still persisting. This illustrates the composition and a distribution of fish species have strong association with the kind of terrestrial landscape elements and highlights the importance of landscape approach to conservation and management of aquatic ecosystems. Occurrence of endangered, endemic and discovery of two new species of Schistura genus re-affirms ‘hottest hotspot’ status of the Western Ghats, a repository of biological wealth of rare kind, both in its aquatic and terrestrial ecosystems. Schistura nagodiensis and S. sharavathiensis are the new fish species of Schistura described from Sharavathi River, central Western Ghats.This also reported the range extension of Schistura nilgiriensis (earlier Nemacheilus nilgiriensis, Jayaram, 1999) from Sharavathi River. (Annexure 1, 2 & 3)

Social Aspects: The sanctuary is having 40 small villages comprising usually of 1 to 10 houses in each village. These villages are situated in valleys where perennial water source and deep soil is available (figure 3.1). None of the settlements are thickly populated. The people naturally move inside the sanctuary as they are depending upon the sanctuary for their fuel, fodder, small timber and other inevitable forest produces required for normal living.

Park zonations:  The sanctuary has been divided in to three zones based on the utility. Spatial extent of each zone is provided in Table 15.

  1. Core Area or Core Zone.
  2. Buffer Area or Buffer Zone.
  3. Tourism Area or Tourism Zone.

Table 15: Zonations ofSharavathi Valley Wildlife Sanctuary

Zone Forest Compt Extent in Ha.
Core zone Karini SF XX -1 to 7 (17) 5102.53
Buffer zone Govardhanagiri SF XX – 1 to 34 13473.68
Buffer zone Channagonda SF (P) XIX – 13 (P) 701.05
Tourism zone Attigodu SF (P) XIX – 1 to 3 763.70
Tourism zone Muppani SF Bl. A XIX – 4 to 7 961.77
Tourism zone Muppani SF Bl. B XIX – 8 to 11 629.16
Tourism zone Sharavathi submerged area   12363.00
Tourism zone Islands within the submerged area   507.00
  Others   8621.11
    TOTAL:- 43123.00


Figure 3.1: Villages in and around SVWS

Humans – Socio-Economic-Energy

Cooking and water heating are the two major end uses that require huge amount of firewood in the region. It is estimated that the average per capita firewood consumption is 1.17 tonnes/year, based on sample survey covering 25% of the villages and 20% of the households. The villagewise cooking and water heating energy consumption values are given in Table 16.1. Estimation of the total fuelwood requirement of the region amounts to 10435 tonnes for the year 1991 and it increased to 15328 during 2001.

Forest biomass availability

Spatial extent of SVWS is about 431 sq.km, with 110 sq.km under semi-evergreen to evergreen forests, 49 sq.km under deciduous forests, 66sq.km under plantations and 90 sq.km under wastelands. Considering the average secondary productivities of each type of forest (3.6 t/h/y for evergreen, 12.5 t/h/y for deciduous, 5 t/h/y for plantations and 0.6 t/h/y for scrub and waste lands), the annual availability of forest biomass as a source of fuelwood is about 189.23x103 tonnes.

Population increase at 3.9% per year has resulted in increased fuel wood demand. Apart from gathering dried and fallen twigs and leaves, local people also cut young saplings, green twigs, and even whole tree. Several plant species preferred by wild animals are being cut for fuel wood as well as for mulching and fodder. Table 16.1, lists the villagewise fuelwood consumption.

Table 16.1: Villagewise per-capita fuelwood consumption (Kg/person/day)

Village Name Cooking Water Heating
Monsoon Winter Summer
Ambargodlu 1.5 1.5 1.2 1.2
Chikkamathur 1.7 1.5 1.3 1.3
Mattikoppa 1.5 1.4 1.2 1.2
Hunalamadike 1.8 2.8 1.7 1.7
Valagere 1.6 1.8 1.4 1.3
Kalasavalli 1.7 1.8 1.4 1.4
Araballi 1.4 1.8 1.4 1.4
Honnemardu 1.8 1.7 1.4 1.4
Baliggere 2.0 2.0 1.3 1.3
Bannumane 1.6 1.4 1.2 1.2
Aravadi 1.7 1.7 1.2 1.2
Brahmana Ilakalale 1.6 1.5 1.2 1.2

At present the domestic energy consumption is well within the total biomass availability from the region. However, with increasing population poses a serious threat to the sustainability of forest resources.

The average livestock holding is in the order of 3.33 buffaloes, 2.27 bullocks and 4.5 cattle per household. Most of the households opt for open grazing in forests that hampers natural regeneration. The estimated total number of livestock in the sanctuary area is 17655. Animal residue (dung) can be used for biogas production, which might minimise the fuelwood pressure on forests. Quantification shows an order of 7627 cu.m to 11122 cu.m per day of biogas generation potential in the region (assuming that a kilogram of fresh animal residue provides 0.03 – 0.042 m3 of gas), which is sufficient to meet the cooking energy needs of 27572 – 21801 persons. However the energy transition from fuelwood to biogas requires policy initiatives as most collect firewood at zero cost due to proximity of forests.

Village forest farms in the selected village would reduce the pressure of cattle on natural forests. Promotion of stall-feeding and conversion of degraded common lands to community fodder farm would bring down the pressure on forests. Village self help groups to be involved in creation and maintenance of village fodder farms in selected villages

Threats and Management

Protected areas (PAs) are established for protecting a particular area with clear management objective. Factors such as encroachment of habitats, poaching and grazing are responsible for the depletion and extinction of wildlife resources. The cases of encroachment of habitats and activities like poaching and grazing are threatening a majority of the wildlife habitats around the world. With the passage of time, human influences on habitats had an alarming impact. SVWS harbours endemics and threatened species of flora and fauna, and hence requires immediate protection and conservation measures. Already large areas of pristine forests have been cleared for hydroelectric-projects, Acacia auruculiformis plantations, and for agricultural operations, etc. The failure in the conservation of reserve forests is visible in many places with the continued process of habitat destruction. The forests need to be protected from human interference that is detrimental to the growth and regeneration of the forest. This requires improved forest security, transparency in forest product utilization, and a stronger political will.

Human and livestock inside the sanctuary

There are 121 villages inside the sanctuary, having higher human and cattle population (Table 16.2), and 59 of them are in protected area (enclosures). Increased human habitats with forest encroachments have seriously affected the wildlife population. The cultivation of Vetiveria sp. (lemon grass) extensively inside the sanctuary areas such as Meghane (located in Buffer zone of the sanctuary) poses serious threat to the wildlife population.

Table 16.2: Human and Cattle population inside the sanctuary area.

Village name Cattle population Human population
Talakalale 154 95
B. Ilakalale 59 487
Karumane 70 453
Aralagodu 66 338
Bannumane 58 355
B.kopparige 26 156
Muppane 38 413
Arodi 16 44
Mandavalli 80 555
Ambargodlu 41 192
Kagarasu 01 18
Hedathri 23 46
Banukuli 105 945
Kanur 45 501
Kanapagaru 114 1524
Gudihithlu 37 367
Nagavalli 142 1242
Balige 47 498
Nelahari 28 284
Uralagallu 23 209
Chennagonda 181 616
Karani 69 617
Kattinkaru 128 1058
Total 1551 11013
Source: KFD, Wildlife Division, Kargal

People depend on forests for livestock grazing, which results in soil compaction and affects natural regeneration. Apart from domestic livestock, a large population of wild cattle is trapped inside the sanctuary (due to the submersion) contributing to grazing pressure throughout the year.

Agriculture and Encroachment: Agricultural practices in the region are traditional and dependent on forests. The forests provide leaf litter, green leaves and fencing material to the farmers. The dense forest patches are the sources of water to the crops. Present study found that the forest encroachments have resulted in increased agricultural lands. It has been found that the land submergence is one of the major reasons for increased land encroachment in the forests. Migrating and migrated population, marginal farmers and economically sensitive households were major contributors of land encroachments. The widespread occurrence of encroachment is observed in the Kanur, Hebbankeri, Meghane and Nagavalli area, where slash and burn practice is prevalent for growing cash crops especially cotton, pepper, lemon grass, ginger, paddy and areca.

NTFP collection: Resource use has been restricted to the buffer zones, where it has been regulated, while core areas are completely closed. An amendment in 1991 to the Wildlife Protection Act of 1972 specifies that, in wildlife sanctuaries, the chief wildlife warden must certify that any manipulation does not harm wildlife, and that the state government approves the manipulation. The major NTFP of the area is leaves of Diospyros melanoxylon and Cinnamomum zeylanicum. Apart from these, on a minor scale, Emblica officinalis, Terminalia chebula, and various medicinal plants, cane, Bambusa sp., and honey are also collected. Destructive methods of collection of NTFP by lopping the branches of trees like, Myristica malabarica, Garcinia gummigutta, Cinnamomum zeylanicum etc. will affect the endemic tree species.

The industrial extraction of timber from the primary evergreen forests in the past has led to the depletion of valuable endemic species and loss of many special habitats such as Myristica swamps.

NTFP collection is totally banned in the core zone of the sanctuary area since it may pose a threat to the endemic tree species and their regeneration. But, in some areas, the community-based approach can be carried out instead of collections done by tenders given to non-locals by the forest department. This approach will be more appealing since each villager will become more responsible for conserving the forests, as removal of a tree would curtail the financial gains through NTFP. Destructive methods of collection of NTFP by lopping the branches of trees have to be stopped.

Timber smuggling: Timber smuggling is reported to be a major problem in the sanctuary area. It is reportedly smuggled even out of the Linganmakki islands, indicating the involvement of some organized groups. The timber smugglers take advantage of the remoteness of the islands from the human settlements for their illegal activities. We have observed timber harvesting at many places like, Karani, Banukuli, Kanur etc., within the sanctuary, calling for greater and effective vigilance from the authorities and the village forest committees (VFCs).

Monoculture Plantation : Large areas of the sanctuary (15.27%) have been planted with monoculture plantations depriving the wildlife of their habitats. Preference of single species in forest plantations is another reason responsible for depletion of fodder for animals. This could become a major drawback to any kind of habitat restoration programmes as well as energy improvement technologies. The practice of planting of acacia and casuarina is still in progress in open areas of Muppane, Aralagodu, Karani, etc. These monoculture plantations have no other advantages to the wildlife, other than aiding as hiding places for some of the small mammals and agricultural pests. Changes in microclimate and huge litter cover in plantations adjacent to the evergreen and semi evergreen forests would inhibit the growth of younger tree species of natural forests.

Grasslands have been converted to monoculture plantations in the forest enclosures like, Madenur, Muppane, and Shashichowka denying the fodder to herbivores like gaur, sambar, spotted deer, etc. The monoculture of any exotic should be strictly discouraged in the areas of high animal population and movement. Any such reforestation activity should be in accordance with the local need and with indigenous species. Gradual shifting of natural plant species in the monoculture plantation areas is to be done. Habitat improvements with fodder plants species preferred by wild animals are to be planted instead of monocultures of acacia, pinus or casuarinas.

Forest Fire: Usually in this sanctuary forest fires are associated with highly fragmented areas. This plays an important role in the distribution of ungulates and bovines. The main reasons for the fire are the dryness of the forest and the deciduous vegetation. Humans on a yearly basis to enhance the growth of grasses burn much of the forest ground vegetation. While fire generally does not kill adult trees, it will effectively destroy the seedlings and young trees, thus preventing tree regeneration, creating senescent forests and eventually leading to the disappearance of forests (Kessler, 2001). Almost every year forest department burnt the grassy blanks in some places to improve the quality of fodder for wild animals; this phenomenon also affects the habitat of burrowing small mammals. The fire has become a major factor in the degradation of forests. In order to restore the vegetation, these forests must be protected from fire, by preventing it by undertaking measures such as creation of awareness on the implication of fire among the local communities and proper maintenance of fire line.

Forest fragmentation : The humid forests, repository of diverse flora and fauna have been subjected to severe habitat fragmentation. Increase in forest fragmentation also gives rise to edge effect with respect to micro climatic changes, species invasion from surrounding vegetation, aetc. Forest fragmentation is a major problem in this sanctuary. Several roads that pass through the sanctuary and Linganmakki reservoir have dissected and cleaved the habitats. Other than these, heavy biotic pressures in terms of encroachments for human settlements, agricultural fields, etc. have contributed significantly to the fragmentation of habitats.

Past land use practices such as shifting cultivation and selective felling have influenced the present-day forest quality and biodiversity patterns, which are evident from the presence of patch and perforated forest in primary forested areas. Wide scale selective felling of tree like Poeciloneuron indicum, Callophylum tomentosum and Lopopetalum wightianum and Artocarpus hirsutus had been carried out since 1921 to 1971 for railway sleepers, match wood and plywood in places like Karani, Govardhangiri and Kanur, which comes in the core and buffer zone of the sanctuary. The study shows that the regeneration of these species especially Poeciloneuron indicum and Palaquium ellipticum in Karani and Kanur is excellent. Selection felling of industrial timbers continued almost to the mid 1980’s, causing considerable impoverishment of forests.

Human-animal conflicts: Due to fragmentation and reduction of natural habitats with the uncontrolled growth of agricultural practices in the sanctuary area over several years has resulted in repeated stress over the forest areas and acted negatively on the wildlife. Conflicts between wildlife and human have emerged as a problem in the arena of wildlife management. The conflicts, which result from the destruction of crops and damage to property, have raised both social as well as conservation issues, both in and outside the sancturary. Efforts to keep animals out of crop fields by wildlife officials have been futile and sometimes result in people perceiving the animals as being malevolent. Thus, human- animal conflict is a common scene over the entire area. Herbivore and omnivore animals like Indian gaur, Indian porcupine, sambar, wild boar, rodents, etc., inflict considerable damage to agricultural crops. Several incidences of sloth bear attack have been reported in the core and buffer zones of the wildlife sanctuary (villages like, Kattinkaru, Karani, Kanur and Kogar). To tackle this problem, fencing the crops is a common procedure, which is detrimental to both wildlife and forests. The fencing material is usually the locally available wooden log, brought from nearby forests. For supplementing the wooden logs, large number of regenerating forest trees were cut down thereby jeopardizing the forest growth itself. These fences act as enclosures for wildlife movement from one place to another.

Hunting is practised as a sport, for subsistence, for crop protection and as a part of religious tradition by many village communities. During night-times, people form groups and go for hunting. A number of communities (Nayaks, Edegaru and Namadari gowdru) in the sanctuary carry out poaching activity. They target on wild animals like mouse deer, rabbit, wild boar, etc., due to which, the wild animal population is decreasing at a rapid rate. People support hunting as it reduces the probable damage to crops. Even some of the birds like spotted dove, cattle egret, pond heron, jungle fowl, peacock etc., are being hunted for meat by the local tribes. Poaching for money is seldom indulged in and gaurs constitute the main victim. Outside people are believed to be coming to the area to carry out this kind of poaching. At least one or two episodes do occur every year. The remoteness of the area and sparsely distributed human settlements are again advantageous to these poachers. In aquatic environment high fishing activity of the local people, licensed fishermen and migratory fishermen has threatened the indigenous fish population along with the endangered tortoise population of the region.

Proposed habitat corridors: Wildlife present in the region are seasonal migrants from adjacent sanctuaries and hence, the corridors used by these animals should be given more attention. Three micro-habitat corridors have been proposed for linking fragmented habitats, so as to have continued link of populations to maintain sufficient viable reproductive groups to permit breeding. Corridors are to be developed with the native species of plants, which meet the food and fodder requirement of fauna during all seasons. Table 16.3 lists the present land-use in the proposed corridors; similarly Figure 3.2 illustrates the regions proposed for corridors.

Channagonda and Kattinkar Corridor:These corridors are proposed in the western side of the sanctuary with evergreen and semi evergreen forests. This region comes under four state forests namely Muppane, Channagonda, Karani and part of Govardhanagiri.

Table 16.3:Details of land-use pattern in the proposed corridors.

Corridor LC_No. Village Name Population Area (ha) Forest (ha) Agriculture (ha) CW (ha) Un.Cultivated (ha)
1 178 Channagonda 861 6391.49 2353.39 139.04 2158.74 1740.32
2 200 Banukuli 380 2250.59 340 80.68 1745.47 84.44
3 209 Mandavalli 425 875.23 0 61.12 760.20 53.91
Note: CW – cultivable waste


Figure 3.2: Proposed wildlife corridors in the SVWS

Corridors 1 is proposed for free movement of sloth bear, sambar and gaur. It has grasslands and barren lands surrounded by a good semi evergreen and evergreen forest. It encompasses the areas like Channagonda, Kanapagaru, Muppane, Aralagodu and Bedrur. This corridor comes in Muppane state forest and Govardhanagiri state forest and has sparsely distributed semi evergreen and moist deciduous forest. This helps animals to migrate to adjoining forests of Talakalale balancing reservoir, Henni and Gerusoppa area.

Corridor 2 is proposed in Banukuli village and has grassland surrounded by semi evergreen and moist deciduous forests (Kanapagaru and Channagonda villages). Corridor 3 comes under Mandavalli village mainly for the movement of tiger, gaur and sambar. This corridor is nearer to Vatemadike village with grasslands interspersed with moist deciduous forest.

Restoration of forest: In order to restore the forest depending on the state of degradation the following list of plants has been recommended. The list of plants recommended for deciduous, semi-evergreen and evergreen degraded patches area given in Table 17.1, 17.2 and 17.3 respectively.

Table 17.1: Plant recommended for restoration of deciduous forests in the sanctuary.

Plant species Common name Ecosystem and human value
Olea dioica Madle EV
Mimusops elengi Ranjalu EV, NTFP
Aporosa lindleyana Salle EV, FR
Dillenia pentagyna Kanagalu EV
Garcinia indica Muruga EV, FR, NTFP
Terminalia paniculata Hunalu EV
Flacourtia montana Mullu sampige EV, FR
Mangifera indica Mavu EV, FR, MD
Syzygium caryophyllatum Kunnerlu EV, FR
Syzygium cumini Neralu EV, FR
Artocarpus heterophylla Halasu EV, FR
Artocarpus gomezianus Wote EV, NTFP

Table 17.2: Plants recommended for restoration of semi-evergreen forests in the sanctuary

Plant species Common name Ecosystem and human value
Aglaia anamallayana Kempunola EV
Artocarpus heterophyllus Halasu NTFP, F
Artocarpus hirsutus Hebbalasu EV, F
Canarium strictum Kaidhupa EV, NTFP
Dimocarpus longan Kendal EV
Garcinia morella Harisina gurgi EV, F
Holigarna arnottiana Sannele holageru EV
Holigarna beddomei Doddele holageru EV
Hopea ponga Haiga EV
Knema attenuata Hedaglu EV
Mimusops elengi Ranjalu EV, NTFP
Vepris bilocularis Mangappe EV
Polyalthia sp.   EV
Mangifera indica Mavu EV, F
Symplocos racemosa Chunga EV

Table 17.3:  Plants recommended for restoration of evergreen forests in the sanctuary

Plant species Common name Ecosystem and Human value
Poeciloneuron indicum Balgi EV
Knema attenuata Hedaglu EV, F
Myristica malabarica Rampatre EV, NTFP
Myristica dactyloides Patre EV, NTFP
Persea macrantha Gulmavu EV
Calophyllum tomentosum Surhonne EV
Dipterocarpus indicus Dhuma EV
Palaquium ellipticum Hadasale EV
Ficus nervosa   EV
Mastixia arborea Niratte EV
Vateria indica Saldhupa EV, NTFP
Elaeocarpus tuberculatus   EV
Mangifera indica Mavu EV, F
Chrysophyllum roxburghii   EV
Canarium strictum Kaidhupa EV
Calamus sp. Betha NTFP
Syzygium gardneri Nerlu EV, FR
Note: EV- Ecosystem value, FR- Fruit, LM- Leaf Manure, MD- Medicinal & NTFP- Non Timber Forest Produce

Policies: In SVWS, forest enclosures play an important role in order to maintain viable wildlife population. Madenur, Muppane, Hallibyle and Shashichowka are the few forest enclosures with high density of gaur, sambar, and mouse deer. The intention of these enclosures is to provide protection to both flora and fauna of the region. These forest enclosures serve a better protection to some of the vulnerable species from the poachers. Most of these enclosures are planted with monoculture species like, Acacia, Casuarina, etc., which in turn not a suitable habitat for the above mentioned wildlife. In order to maintain the high density of these species, gradual conversion of monoculture into native species As the territories of wild animals extend beyond these enclosures, flocking of wild animals and futile attempts to cross these barriers have been noticed. This suggests the expansion of existing enclosures and creation of new enclosures, which has to be undertaken based on rigorous monitoring of wildlife movement.

Effective vigilance has to be exercised by the forest department in order to stop the further encroachments and poaching of wild animals inside the sanctuary. To avoid water scarcity, large number of water holes/percolation ponds should be constructed inside the sanctuary. The existing awareness programmes such as wildlife weeks, wildlife census, etc., have to be expanded and strengthened in the sanctuary and surrounding areas in order to educate and create awareness among local people. Interaction of forest officials with local people helps to arrive at solutions based on clear understanding of situation in the sanctuary.

In the adjoining areas like, Gerusoppa, Uttarakoppa, Aruvakki etc., Kyasanur Forest Disease (KFD) is more prevalent due to high degree of forest degradation, that has led to the extensive growth of weeds, where in ticks, the main disease vector inhabit. Therefore restoration of full-canopied natural forest in the sanctuary area is of paramount importance. The Sharavathi valley wildlife sanctuary has to be extended further so as to link to the Mookambika wildlife sanctuary to facilitate the better movement of wild animals and also conservation of endangered and endemic fauna (like Lion-tailed Macaque) and pristine forest areas (like, Kodachadri, Gurta, Malemane and Kathalekan).

3. GUDAVI BIRD SANCTUARY

Gudavi bird sanctuary is located at 14° 25' 59" to 14° 26'41" N and 75° 6' 43" to 75° 1' 28" E in Soraba Taluk of Shimoga district (Figure 4). The Gudavi Bird Sanctuary was preliminary notified vide government notification No. AHFF-262-FWL-86 Dtd 10.07.1989 of Government of Karnataka and finally notified vide Government notification no. FEE-220-FWL-99 Dtd 4.09.2000 (Karnataka Forest department, 2006). The total area of Gudavi bird Sanctuary is 73.68 Hectares of which water spread area is 33 Ha and is surrounded by moist deciduous forest, interspersed with grassy patches (Karnataka Forest department, 2006). In this sanctuary there are two ponds called as Vaddakere and Gudavi ponds. The catchment area for this sanctuary is mainly agriculture land and other wooded areas. It is surrounded by paddy fields on North, West and Southern sides and dry and on North and Eastern sides. There are three villages namely Hullemaradi, Gudavi and Kallambi with a population of about 3000. Majority of the population are agriculturists.The area is plain and soil is deep and lateritic in origin. The average rainfall of the area is 1500 mm. The maximum and minimum temperature recorded in the sanctuary is 15° C and 38º C respectively. The area surrounding the wetland is covered with dense moist deciduous forest.

Description: C:\Documents and Settings\ENVAS_2003\Desktop\Gudavi.jpg
Figure 4: Gudavi Bird Sanctuary

The boundaries of the sanctuary are:
North: Tank bound and Hinduvaly S.No.199, 201, 211, 71 & 204 of Gudavi village.

East: Gudavi road and Hinduvaly S.No. 55 and 64 of Kallambi village.
South: S.No. 54 & 55 of Kallambi village.

West: Hulemardi road & Hiduvaly S.No. 182.

Composition of vegetation
Mainly five tree species are utilized by birds for nesting – Vitex leucoxylon, Kiranganelia reticulate, Phyllanthus polyphyllus, Ficus lacur and Terminalia sp.

Bird species composition: There are about 191 species of birds, out of 63 species of birds are totally dependent on water. The number of species changes in different months. Highest number of species is observed during October and least number of species in July. (Karnataka Forest department, 2006)

Dayananda G.Y. (2009) studied the bird diversity of Gudavi Bird Sanctuary. The avifauna of Gudavi Bird Sanctuary belonged to 16 orders.Out  of  these members  of  Ciconiformes,  Paliconiformes and  Passeriformes  contributed  maximum  to the  avifauna  of  the  ponds  throughout  the year.  The members  of  order  Anseriformes and  Charadriformes  are  migratory  specieswho  utilize  the  ponds  for  foraging  during winter months. However, the local migrants are  widespread  throughout  the  year  and  to adjacent  wetlands,  moving  to  and  fro utilizing  the  best  resources  available  to them. The total number of species recorded in this sanctuary was 218.Of the  218  species  of  birdssighted  at  the  sanctuary,  a  large  number  of terrestrial birds  (163  species)  constituted 75.11% whereas 24.88% was constituted by a  relatively  small  number  of  aquatic  birds consisting of 54 species. In terms of species strength of families represented Muscicapidae was the largest with 35 species. (Table 18)

Table18: Species composition of birds at Gudavi Bird Sanctuary

SN Common name Scientific Name Residential Status Abundance Status
1. Family: Podicipedidae
1 Little Grebe Tachybaptusruficollis R V Com
2. Family: Phalacrocoracedae
2 Great Cormorant Phalacrocoraxcarbo RM Com
3 Indian Shag Phalacrocoraxfuscicollis RM Com
4 Little Cormorant Phalacrocoraxniger RM L Com
3. Family: Anhingidae
5 Darter or Snake bird Anhingamelamogaster RM L Com
4. Family: Ardeidae
6 Grey Heron Ardeacinerea RM L Com
7 Purple Heron Ardeapurpurea RM L Com
8 Little Green Heron Butoridesstriatus RM Ra
9 Pond Heron Ardeolagrayii R L Com
10 Cattle Egret Bubulcusibis RM Com
11 Large Egret Casmerodiusalbus RM Com
12 Smaller Egret Mesophoyxintermedia RM L Com
13 Little Egret Egrettagarzetta R L Com
14 Night Heron Nycticoraxnycticorax R L Com
15 Chestnut Bittern Ixobrychuscinnamoneus RM L Com
5. Ciconiidae
16 Painted Stork Mycterialeucocephala RM L Com
17 Openbill Stork Anastomusoscitans R L Com
6. Family: Threskiornithidae
18 Black-headed Ibis Threskiornismelanocephalus R L Com
19 Black Ibis Pseudibispapillosa R Un Com
20 Glossy Ibis Plegadisfalcinellus RM Un Com
21 Spoonbill Platalealeucorodia RM L Com
7. Family: Anatidae
22 Lesser whistling Teal Dendrocygnajavanica R L Com
23 Pintail Anusacuta M Com
24 Common Teal Anascrecca RM V Com
25 Spot-billed Duck Anaspoecilorhyncha RM Com
26 Garganey Anasquerquedula M V Com
27 Shoveller Anasclypeata M Com
28 Cotton Teal Nettapuscoromandelianus R L Com
29 Nakta or Comb Duck Sarkidiornismelanotos R Un Com
8. Accipitridae
30 Crested Honey-Buzzard Pernisptilorhyncus R L Com
31 Common P ariahkite Milvusmigrans R Com
32 Brahminy kite Haliasturindus R L Com
33 Shikra Accipiterbadius RM Com
34 Sparrow Hawk Accipiternisus R L Com
35 Besra Sparrow Hawk Accipitervirgatus R L Com
36 Tawny Eagle Aquilarapax RM L Com
37 Greater spotted Eagle Aquilaclanga RM Ra
38 Ring tailed fishing Eagle Haliaeetusleucoryphus M Ra
39 P ale Harrier Circusmacrourus RM L Com
40 P aid Harrier Circusmelanoleucos M Ra
41 Marsh Harrier Circusaeruginosus R L Com
42 Common Kestrel Falcotinnunculus RM L Com
9. Phasianidae
43 Grey Partridge Francolinuspondicerianus R Com
44 Jungle bush Quill Perdiculaasiatica R Com
45 Red Spurfowl Galloperdixspadicea R L Com
46 Grey Jungle fowl Gallussonneratii R Com
47 Common Peafowl Pavocristatus R Com
10. Turnicidae
48 Common Bustard Quail Turnixsuscitator R L Com
11. Rallidae
49 IndianRail   Blue-breasted Banded Rallusstriatus RM Un Com
50 Slaty-legged Banded Crake Rallinaeurizonoides R Un Com
51 Brown Crake Amaurornisakool R Com
52 White breasted Water hen Amaurornisphoenicurus R Com
53 Water Cock Gallicrexcinerea RM L Com
54 Indian Moorhen Gallinulachloropus R Com
55 Purple Moorhen Porphyrioporphyrio RM L Com
56 Coot Fulicaatra R V Com
12. Jacanidae
57 P heasant tailed Jacana Hydrophasianuschirurgus R Un Com
58 Bronze winged Jacana Metopidicusindicus R L Com
13. Charadriidae
59 Red-wattled Lapwing Vanellusindicus R Com
60 Yellow-wattled Lapwing Vanellusmalabaricus M L Com
61 Grey P lover Pluvialissquatarola M Un Com
62 Golden Plover Pluvialisdominica RM Va
63 Little ringed Plover Charadriusdubius M Com
64 Marsh Sandpiper Tringastagnatilis M L Com
65 Spotted Sandpiper Tringaglareola RM L Com
14. Scolopacidae 
66 Common or Fantail Snipe Gallinagogallinago R Com
15. Recurvirostridae
67 Black-winged Stilt Himantopushimantopus R Com
16. Laridae
68 Indian River Tern Sternaaurantia RM L Com
69 Common Tern Sternahirundo R L Com
17. Culumbidae
70 Grey fronted Green Pigeon Treronpompadora R L Com
71 Common Green Pigeon Treronphoenicoptera R Com
72 Green Imperial Pigeon Duculabadia R L Com
73 Blue Rock Pigeon Columbalivia R V Com
74 Spotted Dove Streptopeliachinensis R V Com
 18. Psittacidae
75 Rose ringed P arakeet Psittaculakrameri R V Com
76 Blossom headed P arakeet Psittaculacyanocephala RM L Com
77 Lorikeet Loriculusvernalis RM L Com
 19. Cuculidae 
78 P ied crested Cuckoo Clamatorjacobinus R L Com
79 Common hawk Cuckoo Cuculusvarius R L Com
80 Indian Cuckoo Cuculusmicropterus R L Com
81 Koel Eudynamysscolopacea R V Com
82 Large Greenbilled Malkoha Rhopodytestristis R L Com
83 Small Greenbilled Malkoha Rhopodytesviridirostris R L Com
84 Coucal or Crow-Pheasant Centropussinensis R V Com
85 Lesser Coucal Centropusbengalensis R V Com
 20. Strigidae 
86 Barred Jungle Owlet Glaucidiumradiatum R L Com
87 Spotted Owlet Athenebrama R Com
88 Mottled wood Owl Strixocellata R L Com
89 Brown wood Owl Strixleptogrammica RM L Com
 21. Apodidae
90 Indian edible nest Swiftlet Collocaliaunicolor R Com
91 House Swift Apusaffinis RM Com
 22. Alcedinidae
92 Pied Kingfisher Cerylerudis R Com
93 Small blue Kingfisher Alcedoatthis R Com
94 Stork-billed Kingfisher Pelargopsiscapensis R L Com
95 White-breasted Kingfisher Halcyonsmyrnensis R Com
 23. Meropidae 
96 Chestnut headed Bee-ater Meropsleschenaultia RM L Com
97 Small green Bee-eater Meropsorientalis R L Com
98 Blue bearded Bee-eater Nyctyornisathertoni R L Com
 24. Coraciidae
99 Roller or Blue jay Coraciasbenghalensis R Com
 25. Upupidae
100 Hoopoe Upupaepops R V Com
 26. Bucerotidae
101 Common grey Hornbill Tockusbirostris R Com
102 Malabar Grey Hornbill Tockusgriseus R Com
103 Malabar pied Hornbill Anthracoceroscoronatus R Com
27. Megalaimidae
104 Large green Barbet Megalaimazeylanica R Com
105 Lineated Barbet Megalaimalineate R L Com
106 Small green Barbet Megalaimaviridis R Com
107 Crimson throated Barbet Megalaimarubricapilla R Com
108 Crimson breasted Barbet Megalaimahaemacephala R Com
28. Picidae
109 Rufous Woodpecker Micropternusbrachyurus R L Com
110 LesserWoodpeckergolden backed Dinopiumbenghalense R L Com
111 Great black Woodpecker Dryocopusjavensis R L Com
112 YellowWoodpeckerfronted pied Picoidesmahrattensis R L Com
113 Pigmy Woodpecker Picoidesnanus R L Com
29. Pittidae
114 Indian Pitta Pittabrachyura R Com
30. Alaudidae
115 Bush Lark Mirafraassamica R Com
116 Red winged Bush-Lark Mirafraerythroptera R L Com
117 Black bellied Finch-Lark Eremopterixgrisea RM L Com
118 Rufous tailed Finch-Lark Ammomanesphoenicurus R L Com
119 Crested Lark Galeridacristata R L Com
120 Sykes's Crested Lark Galeridadeva RM L Com
31. Hirundinidae
121 Swallow Hirundorustica RM L Com
122 Wire tailed Swallow Hirundosmithii RM L Com
123 Indian cliff Swallow Hirundofluvicola R L Com
32. Laniidae
124 Rufous backed Shrike Laniusschach R L Com
33. Oriolidae
125 Golden Oriole Oriolusoriolus RM Com
126 Black naped Oriole Orioluschinensis R Com
127 Black headed Oriole Oriolusxanthornus R Com
34. Dicruridae
128 King Crow or Black Drongo Dicrurusadsimilis R Com
129 Grey or Ashy Drongo Dicrurusleucophaeus R Com
130 Racket tailed Drongo Dicrurusparadiseus R Com
35. Sturnidae
131 Brahminy Myna Sturnuspagodarum R Com
132 Indian Myna Acridotherestristis R Com
133 Jungle Myna Acridotheresfuscus R Com
36. Corvidae
134 Tree pie Dendrocittavagabunda R Com
135 White bellied Treepie Dendrocittaleucogastra R Com
136 House Crow Couvussplendens R V Com
137 Jungle Crow Corvusmacrorhynchos R V Com
37. Campephagidae
138 Pied Flycatcher-Shrike Hemipuspicatus R Com
139 Large Wood Shrike Tephrodornisgularis R Com
140 Common Wood Shrike Tephrodornispandicerianus R V Com
141 Black headed cuckoo Shrike Coracinamelanoptera R Com
142 Scarlet Minivet Pericrocotusflammeus R Un Com
143 Long tailed Minivet Pericrocotusethologus R Un Com
144 Small Minivet Pericrocotuscinnamomeus R Com
145 White bellied Minivet Pericrocotuserythropygius R Com
38. Irenidae
146 Common Iora Aegithinatiphia R V Com
147 Marshall's Iora Aegithinanigrolutea R Com
148 Gold fronted Chloropsis Chloropsisaurifrons R Com
39. Pycnonotidae 
149 Red whiskered Bulbul Pycnonotusjocosus R V Com
150 White cheeked Bulbul Pycnonotusleucogenys R Com
151 Red vented Bulbul Pycnonotuscafer R V Com
152 Black Bulbul Hypsipetesmadagascariensis R Com
40. Muscicapidae
Sub Family :Timalinae
153 Spotted Babbler Pellorneumruficeps R Com
154 Slaty headed scimitar Babbler Pomatorhinushorsfieldi R Com
155 Common Babbler Turdoidescaudatus R V Com
156 Large grey Babbler Turdoidesmalcolmi R V Com
157 Jungle Babbler Turdoidesstriatus R V Com
158 White headed Babbler Turdoidesaffinis R Com
159 Wynaad laughing Thrush Garrulaxdelesserti R Un Com
160 Jerdon’s laughing Thrush Garrulaxjerdoni R Un Com
161 White headed shrike Babbler Gampsorhynchusrufulus R Un Com
162 Black capped Sibia Heterophasiacapistrata R Com
Sub Family: Muscicapinae
163 Black and Orange Flycatcher Muscicapanigrorufa RM Un Com
164 Tickll's blue Flycatcher Muscicapatickelliae R Com
165 Verditer Flycatcher Muscicapathalassina R Com
166 Nilgiri verditer Flycatcher Muscicapaalbicaudata R Com
167 White spotted fantail Flycatcher Rhipiduraalbicollis R Com
168 Paradise Flycatcher Terpsiphoneparadise R Com
169 Black naped blue Flycatcher Hypothymisazurea R Com
Sub Family: Sylviinae
170 Rufous fronted Wren-Warbler Priniabuchanani RM Com
171 Ashy Wren-Warbler Priniasocialis M Ra
172 Jungle Wren-Warbler Priniasylvatica M Ra
173 Tailor bird Orthotomussutorius RM V Com
174 Striated marsh Warbler Megaluruspalustris R Un Com
175 Booted Warbler Hippolaiscaligata R Un Com
176 Common Chiffchaff Phylloscopuscollybita R Un Com
177 Large billed leaf Warbler Phylloscopusoccipitalis R Un Com
Sub Family: Turdinae
178 Blue Chat Erithacusbrunneus R V Com
179 Magpie Robin Copsychussaularis RM V Com
180 Shama Copsychusmalabaricus R Un Com
181 Brown rock Chat Cercomelafusca RM Un Com
182 Pied bush Chat Saxicolacaprata R Com
183 Jerdon’s bush Chat Saxicolajerdoni R Com
184 Indian Robin Saxicoloidesfulicata R V Com
185 Blue Rock Thrush Monticolasolitarius R Com
186 Orange headed Thrush Zootheracitrinecyanotus R Com
187 Black Bird Turdusmerula RM Com
41. Paridae
188 Grey Tit Parusmajor RM Com
189 White winged Black Tit Parusnuchalis R Com
190 Yellow cheeked Tit Parusxanthogenys R Com
42. Sittidae
191 Chestnut bellied Nuthatch Sittacastanea R Com
43. Motacillidae 
192 Paddy field Pipit Anthusrufulus R L Com
193 Forest Wagtail Motacillaindica R L Com
194 Yellow Wagtail Motacillaflava R Lcom
195 White Wagtail Motacillaalba R Com
196 Large pied Wagtail Motacillamaderaspatensis R Lcom
44. Dicaeidae 
197 Tickell's Flowerpecker Dicaeumerythrorhynchos R L Com
198 Plain coloured Flowerpecker Dicaeunconcolor R L Com
199 Fire breasted Flowerpecker Dicaeunignipectus R L Com
45. Nectariniidae
200 Purple rumped Sunbird Nectariniazeylonica R Com
201 Small Sunbird Nectariniaminima R Com
202 Maroon breasted Sunbird Nectarinialotenia R Com
203 Purple Sunbird Nectariniaasiatica R Com
204 Little Spider hunter Arachnotheralongirostra R L Com
46. Zosteropidae
205 White Eye Zosteropspalpebrosus RM L Com
47. Ploceidae 
Sub Family : Passerinae 
206 House Sparrow Passerdomesticus R Com
Sub Family: Ploceinae      
207 Baya weaver bird Ploceusphilippinus R Com
208 Balck breasted weaver bird Ploceusbenghalensis R Com
209 Streaked weaver bird Ploceusmanyar R L Com
Sub Family: Estrildinae      
210 Red Munia Estrildaamandava R Com
211 Green Munia Estrildaformosa R Un Com
212 White throated Munia Lonchuramalabarica R Com
213 White backed Munia Lonchurastriata R Com
214 Spotted Munia Lonchurapunctulata R Com
215 Black headed Munia Lonchuramalacca R Com
48. Fringillidae    
Sub Family: Carduelinae
216 Rose Finch Carpodacuserythrinus RM Com
Sub Family: Emberizinae    
217 House Striolated Emberizastriolata R L Com
218 Crested Bunting Emberizalathami R L Com
Status of the birds: WM= Winter migrant, Com= Common, R/LM= Resident with local movements, L Com=Locally common, R= Resident, Un Com= Un common, M= Migratory, V Com= Very common, R/LM/SM=Resident with local as well as summer movements.

External threats

About 8.0 Ha of the sanctuary area has been encroached. The tank is drained by the villagers during summer for agriculture and this disturbs the water bird habitation.

REFERENCES

  1. Dayananda G.Y. (2009). Avifaunal diversity of Gudavi Bird Sanctuary, Sorab, Shimoga Karnataka. Our Nature 7:100-109.
  2. Karnataka Forest Department, Management plan for Sharavathi Wildlife Sanctuary (2001-2006) Deputy Conservator of forests Wildlife division Shimoga.
  3. Karnataka Forest Department, Management plan for Shettihalli Wildlife Sanctuary (2001-2006) Deputy Conservator of forests Wildlife division Shimoga.
  4. Karnataka Forest Department, Management plan for Shettihalli Wildlife Sanctuary (2005-06 to 2014-15). Deputy Conservator of forests Wildlife division Shimoga
  5. Karnataka Forest Department, Management plan for Gudavi Bird Sanctuary (2006-07 to 2015-16) Deputy Conservator of forests Wildlife division Shimoga.
  6. Kumara, H.N.(2007) Impact of local hunting on abundance of large mammals in three protected areas of the Western Ghats, Karnataka. Technical report submitted to Rufford Maurice Laing Foundation, U.K.
  7. Kumara, H.N. and Singh, M. (2005b). Disappearance of elephants in Uttara Kannada. Journal of  Bombay Natural History Society, 102:337
  8. Nair, P.V and Gadgil, M (1978). The status and distribution of elephant population of Karnataka. Journal of the Bombay Natural History Society, 75: 1000-1016.
  9. Pramod Kumar M.P.M., Hosetti B.B., Poornesha H.C. and Raghavendra Gowda H.T. (2007). Butterflies of the Tiger-Lion Safari, Thyaverekoppa, Shimoga, Karnataka, Zoos print Journal 22(8):2805.
  10. Sameer Ali, Rao.G.R, Divakar Mesta, Sreekantha, Vishnu D.Mukri, Subhashchandran M.D., Gururaja K.V., Joshi.N.V, and Ramachandra.T.V, 2007. Ecological Status of Sharavathi Wildlife Sanctuary Sahyadri Conservation series-1, ETR-19. Centre For Ecological Sciences,Indian Institute of Sciences, Bangalore.
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