Journal of Threatened Taxa | www.threatenedtaxa.org | 26 November 2018 | 10(13): 12805–12816

 

 

Avian fauna of Amboli Ghat, Sindhudurg District, Maharashtra State, India

 

Varun Satose 1, Vikrant Choursiya 2, Rakesh Deulkar 3 & Sasikumar Menon 4

 

1,4 Institute for Advanced Training and Research in Interdisciplinary Sciences, Sion, Mumbai, Maharashtra 400022, India 

2 Zoology Department, Bhavan’s College, Andheri, Mumbai, Maharashtra 400058, India 

3 No. 87, Amboli (Bazaar), Sawantwadi, Sindhudurg, Maharashtra 416510, India 

1 vari.devil@gmail.com, 2 madscientist.wilderness@gmail.com (corresponding author), 3 rakeshdeulkar5@gmail.com, 4 spmtdmlab@gmail.com 

 

 

 

doi: https://doi.org/10.11609/jott.2886.10.13.12805-12816  |  ZooBank: urn:lsid:zoobank.org:pub:36EC754D-945F-4C19-9DF4-13EA9DA86E5F

 

Editor: R. Jayapal, SACON, Coimbatore, India.           Date of publication: 26 November 2018 (online & print)

 

Manuscript details: Ms # 2886 | Received 19 March 2017 | Final received 23 October 2018 | Finally accepted 31 October 2018

 

Citation: Satose, V., V. Choursiya, R. Deulkar & S. Menon (2018). Avian fauna of Amboli Ghat, Sindhudurg District, Maharashtra State, India. Journal of Threatened Taxa 10(13): 12805–12816; https://doi.org/10.11609/jott.2886.10.13.12805-12816

 

Copyright: © Satose et al.  2018. Creative Commons Attribution 4.0 International License. JoTT allows unrestricted use of this article in any medium, reproduction and distribution by providing adequate credit to the authors and the source of publication.

 

Funding: It was a self funded project. No funding agency involved.

 

Competing interests: The authors declare no competing interests.

 

Acknowledgements: We would like to thank Dr. Parvish Pandya, Pranad Patil, Shashank Dalvi, and Saurabh Sawant for their valuable contributions towards the checklist and preparation of the manuscript.  We would also like to thank Hemant Ogale and Malabar Nature Conservation Club for their immense help during the fieldwork in the study area.

 

 

 

Abstract: The present report puts forth a systematic checklist of bird species observed at Amboli Ghat in Maharashtra from 2009 to 2012, along with information on their status.  A total of 208 species were recorded, which is around 15% of bird species of the Indian subcontinent.  A family-wise analysis showed that the families Accipitridae and Muscicapidae (14 species each) followed by Ardeidae dominated the avifauna of the region.  The study also revealed that the area consisted of 11 species of birds that are classified under Near Threatened category and two under Vulnerable category of IUCN.  This study highlights the urgent need to conserve the biodiversity-rich area of Amboli Ghat with long-term plans.

 

Keywords: Amboli, avian fauna, diversity, endemic, Western Ghats.

 

 

 

The Western Ghats along the western coast of peninsular India is one of the most ecologically significant biological regions of the world.  These hill ranges are recognized as a unique biogeographic province (Mani 1974), a global biodiversity hotspot (Myers et al. 2000), and as one of the 200 most important eco-regions of the world (Olson & Dinerstein 1998).  Amboli Ghat lies in the Sahyadri Hills of the Western Ghats in the Sindhudurg District of Maharashtra State, India.  It is located at 15.9620N–73.9970E and has an average altitude of approximately 690m.  The highest point is 1,100m and the lowest point is 166m.  The terrain is undulating with steep escarpments and dense forests.  There are three well-defined seasons in Amboli: the monsoon spanning from June to around mid-November, the winter from mid-November to February, and the summer, from March to May.  It is the wettest place in Maharashtra State with an average annual precipitation of 7500mm.  The plant life in Amboli is extremely rich since the climatic conditions give rise to a wide range of habitats.  The habitats range from the tropical semi-evergreen forests, tropical moist deciduous forests, subtropical broadleaf hill forests, tropical dry deciduous forests, tropical thorn vegetation, grasslands, and agricultural lands to wetlands.  The wetlands are mainly formed by the collection of water from streams in abandoned agricultural lands.  In general, the vegetation turns drier as one moves from west to east (into the rain shadow region) across the hills.  Lower elevations on the eastern region receive less than 1,200mm of annual rainfall and contain tropical dry deciduous and thorny forests, with tropical moist deciduous forests in more well-watered areas (Champion & Seth 1968).  With an increase in elevation, tropical semi-evergreen rainforests appear along the higher slopes and ridges.  The western region of the hills tends to have mostly tropical moist deciduous forests with wet evergreen forests at lower elevations.  The former gives way to the latter type as one climbs higher.  The forest is mainly fragmented and the semi-evergreen forest patches occur in isolated pockets.

In less than five years, four new faunal species were described and reported from Amboli.  A species of toad, Xanthophryne tigerinus, was recently described as endemic to Amboli (Biju et al. 2009).  Amboli was reported as one of the type localities of a species of frog Pseudophilautes amboli (Biju & Bossuyt 2009), a new species of coral snake Calliophis castoe (Smith et al. 2012), and a new species of colubrid Dendrelaphis girii (Vogel & Rooijen 2011) .  Other snakes like Ornate Flying Snake and Brown Vine Snake were also sighted in this region.

Birds are considered as useful biological indicators because they are ecologically versatile and live in all kinds of habitats.  Extensive documentation of avian fauna of various regions of the Western Ghats and Maharashtra are available.  Prasad (2003) listed about 450 bird species from western Maharashtra, Abdulali (1981) listed 540 bird species from Maharashtra, and Gole (1998) studied bird species of Sahyadri,; documentation can also be found in Ranjit et al. (1990), Lainer (2004), Padhye et al. (2007), Lawate & Mule (2008), and Kachare et al. (2011).  A systematic study on the avian fauna of Amboli Ghat is wanting.  The aim of our study was to explore the nature of bird assemblage in various macrohabitat types in and around Amboli Ghat.  The finding of this study can provide baseline data for intensive studies in the future.  The study also highlights the ecological significance of this highly biodiverse spot in the Western Ghats of India.

 

Methods

Study area

An area of around 54km2 covering locations like Amboli Town, Papdi, Malai, Chaukul, Mahadevgarh, Parpoli, and adjoining areas (Fig. 1), was explored for the study since each zone varies in its landscape type.  In addition to the slope of the valley of Amboli Ghat, this study also included areas of lower hilly terrains, as the valley is surrounded by hills on almost all sides.  The present study explores areas used for agriculture and human settlements as well as natural habitats such as forest patches, grasslands, streambanks, and scrublands.  Locations around the collection of large wetlands near Papdi were also investigated.  Habitat details of the above-mentioned locations are as follows:

1) Papdi (15.8880N & 74.03720E) – a mostly flat terrain with a slightly undulating land, agricultural fields, and streams present with temporary marshes during monsoon and early winter.

2) Malai Forest (15.9410N & 74.0010E) - dense evergreen forest.

3) Chaukul Road (15.9430N & 74.0310E) – a flat terrain covered with vegetation during monsoon and dry scrub in late winter and summer.

4) Amboli Town (15.9660N & 74.0040E) - human settlements near Amboli reserve forest.

5) Mahadevgarh Road (15.9670N & 73.9900E) - evergreen forest cover with sporadic open grassland patches.

6) Amboli Ghat (15.9340N & 73.9900E) - steep escarpments with moist deciduous and evergreen forests.

7) Parpoli (15.9500N & 73.9750E) - foothills of Amboli receiving maximum rainfall in the study area.  The short grown vegetation remains submerged under water till early winter.  The remaining area is covered by evergreen forests.

Bimonthly surveys were carried out in the selected areas of various habitats from March 2009 to March 2012.  The areas were surveyed using binoculars and digital cameras for documenting bird species.  Direct observations and noting of species sighted were made by walking on the roads and village tracks and through grasslands and agriculture areas.  Monitoring of areas was done in the morning from 6:00 to 10:00 hr as well as in the evening from 15:00 to 19:00 hr. Visits were also made in the afternoons and late evenings to check the activities of the avian fauna at different times.  Birds were identified using widely accepted field guides like Ali & Ripley (1983) and Grimmett et al. (1998,2011).  For taxonomy, species sequence, and nomenclature, we followed Praveen et al. (2016).

The status of birds was assigned based on the following criteria:

1) Resident - if a bird was seen all throughout the year (not necessarily nesting).

2) Winter visitor - if a bird was seen only during the period from December to February.

3) Summer visitor - if a bird was seen only during the period from March to May.

The birds were assigned strictly with reference to the study area on the basis of presence or absence method.  The birds that showed irregular trends of sighting and population fluctuations (non-seasonal) were placed under uncertain status.  Current status of threatened categories was adopted from IUCN Red list (IUCN 2016).

 

 

 

 

Results

A total of 208 species was recorded during the study (Table 1), constituting around 15% of the total species listed in the Indian subcontinent by Grimmett et al. (2011).  Birds from 64 families were recorded.  Family-wise analysis showed that the families Accipitridae and Muscicapidae (14 species each) followed by Ardeidae (10 species) dominated the avian fauna, indicating a healthy bird diversity in the region.  Out of the total species encountered, analysis of data revealed that 165 species were residents, 38 species were winter visitors, two species were summer visitors, and the remaining species have an uncertain status.  The status of three species, European Roller Coracias garrulus, Asian Pied Starling Gracupica contra, and Green Avadavat Amandava formosa, was considered uncertain as they showed irregular trends of sighting and population fluctuations (non-seasonal).  Since there are no habitats appropriate for Green Avadavat in the study area, the individuals sighted could be those escaped from cages.A comparative graph was prepared to see the differences in avian faunal diversity in the locations in the study area which revealed Parpoli region with maximum number of species (181 species of birds) (Figs. 2 & 3). A few bird species like Pompadour Green Pigeon Treron pompadora, Grey-bellied Cuckoo Cacomantis passerinus, Drongo Cuckoo Surniculus lugubris, Blue-faced Malkoha Phaenicophaeus viridirostris, Lesser Golden-backed Woodpecker Dinopium benghalense, Yellow-fronted Pied Woodpecker Dendrocopos mahrattensis, White-naped Woodpecker Chrysocolaptes festivus, Heart-spotted Woodpecker Hemicircus canente and Little Spiderhunter Arachnothera longirostra (Table 1) were sighted only at the low-lying well-wooded region of Parpoli in the study area.  Studies show that habitats with structurally complex matrices have greater potential for supporting the populations of forest birds than open areas such as pastures (Raman 2006).  Sixty-one species of birds are recognized as endemic to India (Praveen et al. 2016), of which 13 were sighted in the study area.  A few birds that showed local seasonal migration due to heavy rainfall in the higher altitude areas of Amboli.

Based on the present study, it can be concluded that there are 11 species of birds in the study area that are struggling for their existence throughout their distributional range and therefore can be placed under threat categories as identified by IUCN (2016).  These species are the Vulnerable Woolly-necked Stork Ciconia episcopus, Nilgiri Wood Pigeon Columba elphinstonii (observed roosting), and Green Avadavat (observed roosting) and the Near Threatened Black-necked Stork Ephippiorhynchus asiaticus, Black-headed Ibis Threskiornis melanocephalus, Oriental Darter Anhinga melanogaster, Pallid Harrier Circus macrourus, River Tern Sterna aurantia, Great Hornbill Buceros bicornis, Malabar Pied Hornbill Anthracoceros coronatus, and Grey-headed Bulbul Brachypodius priocephalus (observed feeding and roosting).  Of these, Grey-headed Bulbul and Nilgiri Wood Pigeon are endemic to the Western Ghats.  Vultures were not encountered in the present study.

 

 

 

Table 1. A systematic checklist of bird species of Amboli Ghat, Maharashtra State, India

 

 

Family

Scientific name

Common name

Status

Sighting location

1

Anatidae

Anas poecilorhynca

Indian Spot-billed Duck

R

AR

2

Phasianidae

Pavo cristatus

Indian Peafowl

R

AR

3

 

Perdicula asiatica

Jungle Bush Quail

R

AR

4

 

Gallus sonneratii

Grey Junglefowl

R, EI

AR

5

 

Galloperdix spadicea

Red Spurfowl

R, EI

AR

6

Podicipedidae

Tachybaptus ruficollis

Little Grebe

R

PP

7

Columbidae

Columba livia

Rock Pigeon

R

AR

8

 

C. elphinstonii

Nilgiri Wood Pigeon

R, EI

AT

9

 

Streptopelia orientalis

Oriental Turtle Dove

R

AR

10

 

S. chinensis

Spotted Dove

R

AR

11

 

Treron pompadora

Pompadour Green Pigeon

R

PR

12

 

T. phoenicoptera

Yellow-legged Green Pigeon

R

AR

13

 

Chalcophaps indica

Emerald Dove

R

AR

14

Podargidae

Batrachostomus moniliger

Sri Lankan Frogmouth

R

CR, ML, MG

15

Caprimulgidae

Caprimulgus indicus

Grey Nightjar

R

AR

16

 

C. atripennis

Jerdon’s Nightjar

R

CR

17

 

C. affinis

Savanna Nightjar

R

AT, CR

18

Apodidae

Hemiprocne coronata

Crested Treeswift

R

PR

19

 

Apus pacificus

Fork-tailed Swift

W

AR

20

 

A. affinis

Indian House Swift

R

AR

21

Cuculidae

Centropus sinensis

Greater Coucal

R

AR

22

 

Phaenicophaeus viridirostris

Blue-faced Malkoha

R

PR

23

 

Clamator jacobinus

Pied Cuckoo

S

AR

24

 

Eudynamys scolopaceus

Asian Koel

R

AR

25

 

Cacomantis passerinus

Grey-bellied Cuckoo

R

PR

26

 

Surniculus lugubris

Drongo Cuckoo

R

PR

27

 

Hierococcyx varius

Common Hawk Cuckoo

R

AR

28

 

Cuculus canorus

Eurasian Cuckoo

W

AR

29

Rallidae

Rallina eurizonoides

Slaty-legged Crake

R

CR

30

 

Zapornia pusilla

Ballion’s Crake

W

PP

31

 

Amaurornis phoenicurus

White-breasted Waterhen

R

AR

32

Ciconiidae

Ciconia episcopus

Woolly-necked Stork

R

PP

33

 

Ephippiorhynchus asiaticus

Black-necked Stork

R

PP

34

Ardeidae

Ixobrychus cinnamoneus

Cinnamon Bittern

R

PP, AT

35

 

Nycticorax nycticorax

Black-crowned Night Heron

R

AR

36

 

Butorides striata

Striated Heron

R

PP

37

 

Ardeola grayii

Indian Pond Heron

R

AR

38

 

Bubulcus ibis

Cattle Egret

R

AR

39

 

Ardea cinerea

Grey Heron

W

PP, AT

40

 

A. purpurea

Purple Heron

R

PP

41

 

A. alba

Greater Egret

R

AR

42

 

A. intermedia

Median Egret

R

AR

43

 

Egretta garzetta

Little Egret

R

AR

44

Threskiornithidae

Threskiornis melanocephalus

Black-headed Ibis

R

PP

45

Phalacrocoracidae

Microcarbo niger

Little Cormorant

R

AR

46

Anhingidae

Anhinga melanogaster

Oriental Darter

R

PP

47

Charadriidae

Vanellus malabaricus

Yellow-wattled Lapwing

W

AT

48

 

V. indicus

Red-wattled Lapwing

R

AR

49

Scolopacidae

Actitis hypoleucos

Common Sandpiper

W

AR

50

 

Tringa totanus

Common Redshank

W

PP

51

 

T. glareola

Wood Sandpiper

W

AR

52

Turnicidae

Turnix suscitator

Barred Buttonquail

R

AR

53

Laridae

Sterna aurantia

River Tern

R

AR

54

Accipitridae

Elanus caeruleus

Black-winged Kite

R

AR

55

 

Pernis ptilorhynchus

Oriental Honey Buzzard

R

AR

56

 

Spilornis cheela

Crested Serpent Eagle

R

AR

57

 

Circaetus gallicus

Short-toed Snake Eagle

R

AR

58

 

Ictinaetus malaiensis

Black Eagle

R

AR

59

 

Aquila rapax

Tawny Eagle

R

AT

60

 

A. fasciata

Bonelli’s Eagle

R

AR

61

 

Hieraaetus pennatus

Booted Eagle

W

AR

62

 

Circus macrourus

Pallid Harrier

W

AR

63

 

C. pygargus

Montagu’s Harrier

W

CR, PP

64

 

Accipiter badius

Shikra

R

AR

65

 

Haliastur indus

Brahminy Kite

R

AR

66

 

Milvus migrans

Black Kite

R

AR

67

 

Butastur teesa

White-eyed Buzzard

R

AR

68

Tytonidae

Tyto alba

Common Barn Owl

R

AR

69

Strigidae

Athene brama

Spotted Owlet

R

AR

70

 

Strix leptogrammica

Brown Wood Owl

R

AR

71

 

Bubo bengalensis

Indian Eagle Owl

R

AR

72

 

Ketupa zeylonensis

Brown Fish Owl

R

AR

73

Bucerotidae

Buceros bicornis

Great Hornbill

R

AR

74

 

Anthracoceros coronatus

Malabar Pied Hornbill

R

AR

75

 

Ocyceros griseus

Malabar Grey Hornbill

R, EI

AR

76

 

O. birostris

Indian Grey Hornbill

R

AR

77

Upupidae

Upupa epops

Common Hoopoe

R

AR

78

Picidae

Picumnus innominatus

Speckled Piculet

R

ML

79

 

Hemicircus canente

Heart-spotted Woodpecker

R

PR

80

 

Dinopium benghalense

Lesser Golden-backed Woodpecker

R

PR, ML

81

 

Micropternus brachyurus

Rufous Woodpecker

R

PR

82

 

Chrysocolaptes festivus

White-naped Woodpecker

R

PR

83

 

Dendrocopos mahrattensis

Yellow-fronted Pied Woodpecker

R

PR

84

Ramphastidae

Psilopogon zeylanica

Brown-headed Barbet

R

PR

85

 

P. viridis

White-cheeked Barbet

R, EI

AR

86

Meropidae

Merops orientalis

Green Bee-eater

R

AR

87

 

M. leschenaulti

Chestnut-headed Bee-eater

R

AR

88

Coraciidae

Coracias benghalensis

Indian Roller

R

AR

89

 

C. garrulus

European Roller

UC

CR

90

Alcedinidae

Ceyx erithaca

Oriental Dwarf Kingfisher

R

AT, CR, ML

91

 

Alcedo meninting

Blue-eared Kingfisher

R

PR, AT

92

 

A. atthis

Common Kingfisher

R

AR

93

 

Ceryle rudis

Pied Kingfisher

R

AR

94

 

Pelargopis capensis

Stork-billed Kingfisher

R

AR

95

 

Halcyon smyrnensis

White-throated Kingfisher

R

AR

96

 

H. pileata

Black-capped Kingfisher

R

PP

97

Falconidae

Falco tinnunculus

Common Kestrel

W

AR

98

 

F. peregrinus

Peregrine Falcon

R

AR

99

Psittaculidae

Psittacula cyanocephala

Plum-headed Parakeet

R

AR

100

 

P. krameri

Rose-ringed Parakeet

R

AR

101

 

Loriculus vernalis

Vernal Hanging Parrot

R

AR

102

Pittidae

Pitta brachyura

Indian Pitta

W

AR

103

Campephagidae

Pericrocotus cinnamomeus

Small Minivet

R

PR

104

 

P. flammeus

Scarlet Minivet

R

AR

105

 

Lalage melanoptera

Black-headed Cuckooshrike

R

PR

106

Oriolidae

Oriolus xanthornus

Black-hooded Oriole

R

PR

107

 

O. kundoo

Indian Golden Oriole

W

AR

108

Artamidae

Artamus fuscus

Ashy Woodswallow

R

PR

109

Vangidae

Hemipus picatus

Bar-winged Flycatcher Shrike

R

PR

110

 

Tephrodornis virgatus

Large Woodshrike

R

MG, PR

111

 

T. pondicerianus

Common Woodshrike

R

PR

112

Aegithinidae

Aegithina tiphia

Common Iora

R

AR

113

Dicruridae

Dicrurus macrocercus

Black Drongo

R

AR

114

 

D. leucophaeus

Ashy Drongo

R

AR

115

 

D. caerulescens

White-bellied Drongo

R

PR

116

 

D. paradiseus

Greater Racket-tailed Drongo

R

PR

117

Rhipiduridae

Rhipidura aureola

White-browed Fantail

R

PR

118

 

R. albicollis

White-throated Fantail

R

PR

119

Laniidae

Lanius schach

Long-tailed Shrike

R

AR

120

 

L. vittatus

Bay-backed Shrike

R

AR

121

Corvidae

Dendrocitta vagabunda

Rufous Treepie

R

PR

122

 

Corvus splendens

House Crow

R

AR

123

 

C. macrorhynchos

Large-billed Crow

R

AR

124

Monarchidae

Hypothymis azurea

Black-naped Monarch

R

AR

125

 

Terpsiphone paradisi

Indian Paradise-flycatcher

R

AR

126

Dicaeidae

Dicaeum agile

Thick-billed Flowerpecker

R

AR

127

 

D. erythrorhynchos

Pale-billed Flowerpecker

R

AR

128

 

D. concolor

Plain Flowerpecker

R

AR

129

Nectariniidae

Arachnothera longirostra

Little Spiderhunter

R

PR

130

 

Leptocoma zeylonica

Purple-rumped Sunbird

R

AR

131

 

L. minima

Crimson-backed Sunbird

R, EI

AR

132

 

Cinnyris asiaticus

Purple Sunbird

R

AR

133

 

Aethopyga vigorsii

Vigors’s Sunbird

R, EI

AR

134

Irenidae

Irena puella

Asian Fairy Bluebird

R

PR

135

 

Chloropsis aurifrons

Golden-fronted Leafbird

R

AR

136

Ploceidae

Ploceus philippinus

Baya Weaver

R

AR

137

Estrildidae

Amandava formosa

Green Avadavat*

UC, EI

AT

138

 

Euodice malabarica

Indian Silverbill

R

PR

139

 

Lonchura striata

White-rumped Munia

R

AR

140

 

L. punctulata

Scaly-breasted Munia

R

AR

141

 

L. malacca

Black-headed Munia

R

AR

142

Passeridae

Passer domesticus

House Sparrow

R

AR

143

 

Gymnoris xanthocollis

Yellow-throated Sparrow

R

PR

144

Motacillidae

Dendronanthus indicus

Forest Wagtail

W

ML, MG, CR

145

 

Anthus rufulus

Paddyfield Pipit

R

AR

146

 

Motacilla cinerea

Grey Wagtail

W

AR

147

 

M. citreola

Citrine Wagtail

W

AR

148

 

M. maderaspatensis

White-browed Wagtail

W

AR

149

 

M. alba

White Wagtail

W

AR

150

Fringillidae

Erythrina erythrina

Common Rosefinch

W

AR

151

Paridae

Parus cinereus

Cinereous Tit

R

PR

152

 

P. xanthogenys

Black-lored Tit

R

AR

153

Alaudidae

Galerida malabarica

Malabar Lark

R, EI

AR

154

Cisticolidae

Prinia hodgsonii

Grey-breasted Prinia

R

PR

155

 

P. socialis

Ashy Prinia

R

AR

156

 

P. inornata

Plain Prinia

R

AR

157

 

Orthotomus sutorius

Common Tailorbird

R

AR

158

Acrocephalidae

Acrocephalus dumetorum

Blyth's Reed Warbler

W

AR

159

 

A. agricola

Paddyfield Warbler

W

AR

160

Hirundinidae

Cecropis daurica

Red-rumped Swallow

R

AR

161

 

Hirundo smithii

Wire-tailed Swallow

R

AR

162

 

H. rustica

Barn Swallow

R

AR

163

 

Ptyonoprogne concolor

Dusky Crag Martin

R

AR

164

Pycnonotidae

Hypsipetes leucocephalus

Black Bulbul

R

AR

165

 

Pycnonotus melanicterus

Flame-throated Bulbul

R

PR, GT

166

 

P. jocosus

Red-whiskered Bulbul

R

AR

167

 

P. cafer

Red-vented Bulbul

R

AR

168

 

Brachypodius priocephalus

Grey-headed Bulbul

R, EI

AR

169

 

Acritillas indica

Yellow-browed Bulbul

R

AR

170

Phylloscopidae

Phylloscopus collybita

Common Chiffchaff

W

AR

171

 

P. tytleri

Tytler’s Leaf Warbler

W

PR

172

 

P. affinis

Tickell's Leaf Warbler

W

PR, ML

173

 

Seicercus nitidus

Green Leaf Warbler

W

AR

174

 

S. trochiloides

Greenish Leaf Warbler

W

AR

175

Sylviidae

Curruca crassirostris

Eastern Orphean Warbler

W

PR

176

 

C. curruca

Lesser Whitethroat

W

PR

177

 

Chrysomma sinense

Yellow-eyed Babbler

R

PR

178

Zosteropidae

Zosterops palpebrosus

Oriental White-eye

R

PR

179

Timaliidae

Pomatorhinus horsfieldii

Indian Scimitar Babbler

R

AR

180

 

Dumetia hyperythra

Tawny-bellied Babbler

R

AR

181

 

Rhopocichla atriceps

Dark-fronted Babbler

R

PR

182

Pellorneidae

Pellorneum ruficeps

Puff-throated Babbler

R

AR

183

Leiothrichidae

Alcippe poioicephala

Quaker Tit Babbler

R

AR

184

 

Argya malcolmi

Large Grey Babbler

R

AT

185

 

A. subrufa

Rufous Babbler

R, EI

AR

186

 

Turdoides striata

Jungle Babbler

R

AR

187

Sturnidae

Pastor roseus

Rosy Starling

W

AR

188

 

Gracupica contra

Asian Pied Starling

UC

AR

189

 

Sturnia pagodarum

Brahminy Starling

R

AR

190

 

Acridotheres tristis

Common Myna

R

AR

191

 

A. fuscus

Jungle Myna

R

AR

192

 

Gracula religiosa

Hill Myna

R

AR

193

Muscicapidae

Copsychus saularis

Oriental Magpie Robin

R

AR

194

 

Kittacincla malabaricus

White-rumped Shama

R

AR

195

 

Muscicapa dauurica

Asian Brown Flycatcher

W

AR

196

 

Cyornis pallidipes

White-bellied Blue Flycatcher

R, EI

CR, ML, PR, MG

197

 

C. tickelliae

Tickell’s Blue Flycatcher

R

AR

198

 

C. rubeculoides

Blue-throated Flycatcher

W

MG

199

 

Eumyias thalassinus

Verditer Flycatcher

W

AR

200

 

Larvivora brunnea

Indian Blue Robin

W

AR

201

 

Myophonus horsfieldii

Malabar Whistling Thrush

R, EI

AR

202

 

Ficedula parva

Red-breasted Flycatcher

W

ML, PR

203

 

Monticola cinclorhynchus

Blue-capped Rock Thrush

W

ML, PR

204

 

M. solitarius

Blue Rock Thrush

W

AR

205

 

Saxicola maurus

Siberian Stonechat

W

CR, PR

206

 

S. caprata

Pied Bushchat

R

AR

207

Turdidae

Geokichla citrina

Orange-headed Thrush

R

AR

208

 

Turdus simillimus

Indian Blackbird

S

AR

 

EI - endemic to India (from Praveen et al. 2016), * - sighted once.

Abbreviations for location: PR - Parpoli region, GT - Ghat region, AT - Amboli Town, CR - Chaukul Road, ML - Malai region, PP - Papdi region, MG - Mahadevgarh region, AR - all regions

 

 

Discussion

A list with authentic records reflects the true natural diversity of the avian fauna of any region.  For taxa that are widespread or migrating, records in such lists form an essential part of the information that can be used to map their global distribution and seasonal movements.  The Amboli Ghat area still provides some potential habitats for the declining population of many bird species.  During the breeding season, Grey-headed Bulbuls were observed foraging in areas of Amboli Ghat dominated by sub-canopy trees bearing fruits.  Fruit availability is also an important factor that decides the breeding season of this species (Balakrishnan 2011).  The occurrence of Malabar Grey Hornbill can be attributed to the retention of fruits in the canopy, which provides food for the species (Raman & Mudappa 2003).  Open areas are of utmost importance for bird populations as these areas provide better visibility for vigilance against predators and free movement for food procurement (Desai & Shanbhag 2012).  It is the need of the hour to monitor these areas systematically in the rapidly changing environment with a focused study on the status, distribution, and conservation of the avian fauna of the region, which can be achieved only through strengthening public participation species.

One of the problems faced by Amboli Ghat in the recent years is the disturbance caused by humans along with deforestation for plantation, development, and mining.  Changes in vegetation components could affect the availability of food resources and microclimatic conditions, which could then affect the richness and abundance of bird species (Johns 1991).

Animals in protected areas may face interference in their daily activities due to tourists and their associated activities.  Tourism in protected areas can have negative influences on animal populations, as tourists often seek out rare or spectacular species during sensitive times such as breeding or nesting (Knight & Cole 1995).  Where human traffic is frequent, species withdraw, change behaviour, or become habituated to human presence (Griffiths & van Schaik 1993).  During the current study, Blue-capped Rock Thrush Monticola cinclorhynchus, Yellow-browed Bulbul Acritillas indica, and Quaker Tit Babbler Alcippe poioicephala were found feeding on garbage left by tourists.

Amboli Ghat is visited extensively by tourists and most of the tourist activities are concentrated around the Amboli Waterfall on State Highway 121 on the outskirts of Amboli Town.  Good connectivity by roads to Karnataka, Goa, and the rest of Maharashtra State results in about 15,000 tourists visiting Amboli during weekends between July and September.  During this period, the roadsides are littered without care.  During the study period, it was revealed that around 20,000 vehicles pass through the study area, mainly Amboli Town on State Highway 121, which results in a number of roadkills and affects the feeding and nesting of birds.  It was found that species like Oriental Dwarf Kingfisher Ceyx erithaca at Amboli are vehemently sought after by photographers and their enthusiasm has disturbed some of their favourite nesting sites.  There are three main motorable roads in Amboli Ghat area.  During monsoon, an average of around 24 roadkills of animals, mainly composing of reptiles and amphibians, are recorded per day.  Most of these reptile and amphibian species were from the Endangered category of the IUCN Red Data Book (IUCN 2016) and were observed on all the motorable roads each day during the study period.  The strategy of biodiversity conservation is based on applying methods of protection in a specified area.  Tourism development must be carefully managed to avoid turning Amboli Ghat into yet another tourist town where bottles, wrappers, plastics, and billboards dominate the landscape.  Though ecotourism is capable of generating high revenue for natural areas that need protection, planning and development of infrastructure pertaining to tourism, its marketing should focus on conservation of nature, minimizing negative visitor impact, and involvement and employment of local populations in all aspects of business operations.  Commercialization programs should have policies to meet higher social and environmental goals like building ecolodges powered by alternative energy resources and allowing travellers to stay in relative comfort while having magnificent wildlife-viewing from their doorsteps, which minimally impacts the local environment.

The following management strategies can be implemented at Amboli Ghat (Wood 2002):

1) Provide adequate budget to conserve popular tourist areas and earmark tourism fees for conservation.

2) Tourism businesses should pay impact fees that should fund infrastructure for solid waste treatment, sewage treatment, electricity, water and tourists must receive clear incentives for conserving water and electricity.

3) Environmental impact monitoring programs should be regularly implemented.

4) Well-managed trails and camping areas should be clearly marked with rules for low-impact use.

5) Restrictions should be in place for the type of vehicles permitted in specific zones, speed limits, dumping of waste, and off-road driving.

6) Training programs should be initiated at local levels to provide local inhabitants with the opportunity to run their own businesses.

 

References

 

Abdulali, H. (1981). Checklist of the Birds of Maharashtra with Notes on their Status around Bombay, Maharashtra. Bombay Natural History Society, Bombay, 16pp.

Ali, S. & S.D. Ripley (1983). Compact Edition of Handbook of the Birds of India and Pakistan. Bombay Natural History Society and Oxford University Press, Bombay, 737pp.

Almeida, S.M. (1990). The Flora of Sawantwadi, Maharashtra, India. Journal of Economic & Taxonomic Botany, Additional Series 2 Volumes. Scientific Publishers, Jodhpur, pp.1-411 & pp.1-304pp.

Balakrishnan, P. (2011). Breeding biology of the Grey-headed Bulbul Pycnonotus priocephalus (Aves: Pycnonotidae) in the Western Ghats, India. Journal of Threatened Taxa 3(1): 1415–1424; https://doi.org/10.11609/JoTT.o2381.1415-24

Biju, S.D. & F. Bossuyt (2009). Systematics and phylogeny of Philautus Gistel, 1848 (Anura, Rhacophoridae) in the Western Ghats of India, with descriptions of 12 new species. Zoological Journal of the Linnean Society 155(2): 374–444.

Biju, S.D., I. Van Bocxlaer, V.B. Giri, S.P. Loader & F. Bossuyt (2009). Two new endemic genera and a new species of toad (Anura: Bufonidae) from the Western Ghats of India. BMC Research Notes 2(1): 241; https://doi.org/10.1186/1756-0500-2-241

BirdLife International (2014). IUCN Red List for birds. http://datazone.birdlife.org/species/spcredcat. Downloaded on 01 January 2014.

Bookbinder, M.P., E. Dinerstein, A. Rijal, H. Cauley & A. Rajouria (1998). Ecotourism’s support of biodiversity conservation. Conservation Biology 12(6): 1399–1404.

Boora, S. (2005). Ecotourism and environmental sustainability in India. Bulletin of the National Institute of Ecology 15: 249–258.

Brown, K. & D.W. Pearce (eds.) (1994). The Causes of Tropical Deforestation: The Economic and Statistical Analysis of Factors giving rise to the Loss of the Tropical Forests.  University College London Press Ltd, London, United Kingdom, 341pp.

Champion, H.G. & S.K. Seth (1968). A Revised Survey of the Forest Types of India, Vol. 1. Manager of Publications, New Delhi, India, 404pp.

Cincotta, R.P., J. Wisnewski & R. Engelman (2000). Human population in the biodiversity hotspots. Nature 404(6781): 990–992.

Daniels, R.J.R, N.V. Joshi, & M. Gadgil (1990). Changes in the bird fauna of Uttara Kannada, India, in relation to changes in land use over the past century. Biological Conservation, 52 (1): 37-48.

Daniels, R.J.R., M. Gadgil & N.V. Joshi (1995). Impact of human extraction on tropical humid forests in the Western Ghats Uttara Kannada, south India. Journal of Applied Ecology 32(4): 866–874.           

Desai, M. & A.B. Shanbhag (2012). An avifaunal case study of a plateau from Goa, India: an eye opener for conservation of plateau ecosystems. Journal of Threatened Taxa 4(3): 2444–2453; https://doi.org/10.11609/JoTT.o2480.2444-53

Gole, P. (1998). Birds of the Sahyadri. Journal of Ecological Society 11: 5–28.

Griffiths, M. & C.P. van Schaik (1993).The impact of human traffic on the abundance and activity periods of Sumatran rain forest wildlife. Conservation Biology 7(3): 623–626.

Grimmett, R., C. Inskipp & T. Inskipp (1998). Birds of the Indian Subcontinent. Christopher Helm Publishers Ltd., London, United Kingdom, 219pp.

Grimmett, R., C. Inskipp & T. Inskipp (2011). Birds of the Indian Subcontinent. Christopher Helm Publishers Ltd., London, United Kingdom, 528pp.

IUCN (2016). IUCN Red List of Threatened Species, Version 2016.1. https://www.iucnredlist.org/ . Downloaded on 30 December 2016.

Jathar, G.A. & A.R. Rahmani (2006). Endemic birds of India. Buceros 11(2&3): 5–53.

Johns, A.D. (1991). Responses of Amazonian rainforest birds to habitat modification. Journal of Tropical Ecology 7(4): 417–437.

Kachare, V.S. R.S. Pawar & D.B. Panaskar (2011). Disturbances on the living of birds and their population in wetlands of Kolhapur City, Maharashtra, India. European Journal of Experimental Biology 1(1): 43–50.

Kale, M.P. G. Talukdar, R.K. Panigrahy & S. Singh (2010). Patterns of fragmentation and identification of possible corridors in north Western Ghats. Journal of the Indian Society of Remote Sensing 38(3): 401–413.

Knight, R.L. & D.N. Cole (1995). Wildlife responses to recreationists, pp. 51–62. In: Knight R.L., & K. Gutzwiller Wildlife and Recreationists Coexistence through Management and Research. Island Press, Washington DC, United States of America, 389pp

Lainer, H. (2004). Birds of Goa: A Reference Book. Goa Foundation, Mapusa, Goa, 244pp.

Lawate, D. & M. Mule (2008). Birds of Chandoli National Park of Western Ghat of Maharashtra. Electronic Journal of Environmental Sciences 2: 13–18.

Mani, M.S. (1974). Biogeographical Evolution in India. pp698–724. In: Mani, M.S. (eds.) Ecology and Biogeography in India. Dr. W. Junk Publishers, The Hague, 724pp.

Myers, N., R.A. Mittermeier, C.G. Mittermeier, G.A. Da Fonseca & J. Kent (2000). Biodiversity hotspots for conservation priorities. Nature 403(6772): 853–858.

Olson, D.M. & E. Dinerstein (1998). The global 200: a representation approach to conserving the earth’s most biologically valuable ecoregions. Conservation Biology 12(3): 502–515.

Padhye, A.D., M. Paingankar, N. Dahanukar & S. Pande (2007). Season and landscape element wise changes in the community structure of avifauna of Tamhini, northern Western Ghats, India. Zoo’s Print Journal 22(9): 2807–2815; https://doi.org/10.11609/jott.zpj.1706.2807-15

Prasad, A. (2003) Annotated checklist of the birds of western Maharashtra. Buceros 8(2&3): 1–174.

Praveen, J., R. Jayapal & A. Pittie (2016). A checklist of the birds of India. Indian Birds 11(5&6): 113–172.

Quantum GIS Development Team (2016). QGIS Geographic Information System. Open Source Geospatial Foundation. https://qgis.org/en/site/

Raman, T.R.S. (2006). Effects of habitat structure and adjacent habitats on birds in tropical rainforest fragments and shaded plantations in the Western Ghats, India. Biodiversity and Conservation 15(4): 1577–1607.

Raman, T.S. & D. Mudappa (2003). Correlates of hornbill distribution and abundance in rainforest fragments in the southern Western Ghats, India. Bird Conservation International 13(3): 199–212.

Smith, E.N., H. Ogale, V. Deepak & V.B. Giri (2012). A new species of coral snake of the genus Calliophis (Squamata: Elapidae) from the west coast of peninsular India. Zootaxa 3437: 51–68.

Urfi, A.J., M. Sen, A. Kalam & T. Meganathan (2005). Counting birds in India: methodologies and trends. Current Science 89(12): 1997–2003.

Vogel, G. & J. Van Rooijen (2011). A new species of Dendrelaphis (Serpentes: Colubridae) from the Western Ghats,  India. Taprobanica 3(2): 77–85.

Wood, M.E. (2002). Ecotourism: Principles, Practices and Policies for Sustainability. United Nations Publications, New York, 64pp.