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Biological Forum – An International Journal 6(2): 7-15(2014) 
ISSN No. (Print): 0975-1130 
ISSN No. (Online): 2249-3239 
Butterfly Fauna (Order: Lepidoptera) in Five Major Tea Gardens of 
Sivasagar District, Assam, India 
Atanu Bora* and L.R. Meitei* 
*Research Scholar, Department of Life Science and Bioinformatics, 
Assam University, Silchar, Cachar District, Assam, India 
(Corresponding author: Atanu Bora) 
(Received 08 July, 2014, Accepted 09 August, 2014) 
ABSTRACT: The present paper is based on observations and sighting records of butterfly fauna fromMarch 
2012 to February 2013 in five major Tea Gardens, Sivasagar District of Assam, India. The district has 119 tea 
estates which covers an area of 88, 008 hectares of land. The beautiful tea gardens provide a very attractive 
landscape to the district. Based on the study of butterfly diversity in the study area, a checklist has been 
prepared. A total of 104 butterfly species belonging to 5 families of order Lepidoptera were recorded during 
the study period. The family Nymphalidae, represented by 46 species was the most dominant followed by 
Lycaenidae (23 species), Hesperiidae (13 species), Pieridae (13 species) and Papilionidae (9 species) being the 
least. From the conservation point of view, the study areas are undisturbed and rich in butterfly fauna. 
Keywords: Tea gardens, Sivasagar District, Assam, India, butterfly species. 
INTRODUCTION 
Geographically, the state of Assam is situated between 
24°10’ to 27°58’ N latitude and 89°49’ to 97°26’ E 
longitude. Sharing its borders with Arunachal Pradesh 
on the north; Nagaland, Manipur and Arunachal 
Pradesh on the east; Meghalaya, Mizoram and Tripura 
on the south and Meghalaya on the west, Assam is 
located on the north-eastern part of the Indian sub-continent. 
The state is connected with the rest of the 
Indian Union by a narrow corridor in West Bengal that 
runs for 56 Kms. below the foothills of Bhutan and 
Sikkim. The prime geographical characters that form 
the topographical features of Assam are the Barak 
Valley and the River of Brahmaputra. 
The state occupies a total area of about 78,523 sq km. 
placed on the foothills of the majestic Himalaya, Assam 
Forest covers a major part of the total land available in 
the state. Going by a survey conducted by the Forest 
Department of Assam Government, in the year 2003, 
the state possessed a total of 26, 781.91 sq km forest 
land. Bamboo and timber are the two prime forest 
products of Assam. The specialty of Assam Climate lies 
in its highest levels of humidity. Assam is known to 
have maximum amount of rainfall. The temperatures 
never go beyond the standard 35° to 38°C. While, the 
hilly regions of Assam experience a suitable sub-alpine 
climatic condition, the plain lands of the state go 
through excessive humid weather. Primarily, the 
climate of Assam is categorized under two prime heads 
- rainy season and winter months. 
The rainy season starts from June while the winter 
months begin with the onset of October. The minimum 
temperature which is found in the coldest of months in 
Assam ranges from 6 to 8°C. 
Assam is the world's largest tea growing region and not 
only famous for its quality of tea as well as the natural 
beauty of the tea plantation area. Beautiful tea estates of 
Assam cover about 2, 16, 200 hectares of land 
comprises of more than 100 tea estates. Enormously 
found mountain region, its greenery and pleasant 
climate make this location popular not only for its tea, 
but also for being a popular spot for enjoying eco-vacations. 
The both sides of the famous river, 
Brahmaputra, constitute the world's largest Tea growing 
area. The tea plants are grown in the lowlands of 
Assam, unlike Darjiling and Nilgiris, which are grown 
in the highlands. The Assam tea bush grows in a 
lowland region, in the valley of the Brahmaputra River, 
an area of clay soil rich in the nutrients of the 
floodplain. The climate varies between a cool, and 
winter and hot, humid rainy seasons- the conditions 
ideal for growing tea. Because of its lengthy growing 
seasons and generous rainfall of about 250-300 mm 
(during the monsoon season), Assam is one of the most 
prolific tea-producing region in the world. This region 
of India is so famous for its tea plantation that Assam 
tourism has organized the Assam Tea festival in the 
month of November every year that makes a totally 
new experience to enjoy this place.
Bora and Meitei 8 
MATERIAL AND METHODS 
Study Area. The present study was conducted to study 
the diversity of butterfly fauna in five major tea gardens 
of Sivasager district, Assam, India from March 2012 to 
February 2013. Sivasagar district is situated in the 
North-Eastern part of Assam between 94.25° to 95.25° 
N latitude and 26.45° to 27.15° E longitude. It is placed 
in 99 meters to 103 meters elevation range above sea 
level. 
Fig.1. Location map of Sivasagar District showing study sites.
Bora and Meitei 9 
The district is surrounded by Lakhimpur and Dibrugarh 
in the north, Arunachal Pradesh and Dibrugarh in the 
east, Arunachal Pradesh and Nagaland in the south, 
Jorhat district of Assam in the west. The Naga Hills lie 
towards the south, while the Brahmaputra River is on 
the north. The district is located at Upper Brahmaputra 
Valley of Agro-climatic zone of the state and occupies 
a total geographical area of 2668 sq.km. The district is 
situated in the humid sub-tropical region and 
characterized by heavy rainfall and high relative 
humidity above 90%; high temperature up to 38°C is 
observed in the summer season and comparatively low 
temperature up to 7°C in winter. The soils of this zone 
is immature alluvial in char to mature ultisol in the 
piedmont high and hill areas. The vegetation is mostly 
tropical evergreen with trees like Hollong, Titachapa, 
Nahor, Mekai etc. dominating the forest canopy. 
Sivasagar’s biggest contribution to the world is its tea 
plantation. There are 119 tea estates in the district 
which covers an area of 88, 008 hectares. Besides these 
tea estates, 80 registered small tea growers and 4, 004 
small tea growers covers the 5356 hectares of land in 
this district. The district produces some of the finest and 
most expensive teas in the world. Tea gardens of the 
district not only produce economy but also it adds the 
scenic beauty. The beautiful tea gardens provide a very 
attractive landscape to the district. 
The five major tea gardens of the district where the 
study was conducted are as follows – 
Sector 1: Maskara Tea Estate, P.O. Rajmai: Total area 
under tea cover is 44.71 hectares. 
Sector 2: Bezbaruah Tea Estate, P.O. Sapekhati: Total 
area under tea cover is 89.43 hectares. 
Sector 3: Aideobari Tea Estate, P.O. Sonari: Total area 
under tea cover is 150.65 hectares. 
Sector 4: Bemolapur Tea Estate, P.O. Borhat: Total 
area of the estate is 1214 hectares, out of which 527 
hectares is under tea cover. 
Sector 5: Behubor Tea Estate, P.O. Nazira: Total area 
under tea cover is 533.86 hectares. 
Taxonomic Study. Field notes, photographs (camera: 
Nikon d5100) and observations of butterflies were 
taken for the entire growing season during the day light 
hours. The population trends of butterflies were 
monitored for one year using transects counting method 
(Barhaum et al., 1980). Butterflies were netted only 
when necessary to prevent the possibility of handling 
effect (Morton, 1984). Species were noted along with 
the date, location of capture and any plant association. 
Other factors noted include the time of day using a 
twenty-four hour clock and the weather conditions. At 
each location the same route of inspection was followed 
each time to reduce the number of variables presents 
(Pyle, 1984) and to avoid any personal difference all the 
counts were made by the same person. 
An effort has been made to use the latest nomenclature 
and common names as far as possible as per Evan 
(1932), D’ Abrera (1982-1986), Varshney (1990) and 
Kehimkar (2008). The relative abundance or say status 
of individual species is categorized within the tea 
gardens as “Very Rare” (VR) when recorded rarely; 
“Rare” (R) when recorded occasionally; 
“Uncommon” (UC) when recorded frequently; 
“Common” (C) when recorded regularly; “Very 
Common” (VC) when recorded regularly in large 
numbers. 
RESULT AND DISCUSSION 
During the study, a total of 104 species belonging to 72 
genera under 5 families were recorded from the selected 
five major tea garden areas (Table 1). The family 
Nymphalidae showed the maximum species richness, 
comprising of 27 genera and 46 species, followed by 
Lycaenidae (21 genera, 23 species), Hesperiidae (12 
genera, 13 species), Pieridae (9 genera, 13 species) and 
Papilionidae (3 genera, 9 species) being the least (Fig. 
2). Abundance showed that out of the 104 butterfly 
species recorded, 33 are uncommon, 39 are common, 
11 are very common, 12 are rare and 9 are very rare to 
the study area. A total of 5696 individuals were 
recorded from the five tea gardens, of which the Sector 
5 representing the Behubor Tea Estate contributing 
1587 individuals was dominant while the Sector 1 
representing the Maskara Tea Estate with 941 
individuals was the least (Fig. 3). Eurema hecabe 
(Linn.) was the most dominant species of butterfly in 
terms of number of individuals (156) followed by 
Papilio polytes (Linn.) (150), Pieris canidia (Sparrman) 
(142), Catopsilia pomona (Fabricius) (141), Ypthima 
baldus (Fabricius) (138) and 6 other species in the 
study area (Table 1, *Marked Asterisks). Discophora 
timora (Westwood) and Mycalesis gotama (Moore) (3 
individuals each) were the rarest species followed by 
Chliaria othona (Hewitson) (4), Polyura agraria 
(Swinhoe) (4) and 5 other species (Table 1, #Marked 
Asterisks). 
Results suggested that the family Nymaphalidae 
with 27 genera and 46 species was the most 
dominant in the study area. Members of the 
Nymphalidae were always dominant in the tropical 
region because most of the species are polyphagous in 
nature, consequently helping them to live in all the 
habitats. Additionally, many species of this family are 
strong, active fliers that might help them in searching 
for resources in large areas (Eswaran and Pramod 2005; 
Krishna Kumar et al. 2007). A high proportion of 
nymphalid species thus clearly indicates high host plant 
richness in the study areas.
Bora and Meitei 10 
Table 1: Checklist of Butterflies and their abundance recorded in selected five major Tea Gardens, Sivasagar 
District, Assam. 
Sl. 
No. 
Scientific Name Sector 1 Sector 2 Sector 3 Sector 4 Sector 5 Total Relative 
Abundance 
Family: Hesperiidae 
1. Bibasis oedipodea 
(Swainson) 
05 04 02 00 06 17 UC 
2. Hasora chromus (Cramer) 02 06 02 02 05 17 UC 
3. Pseudocoladenia dan 
(Fabricius) 
12 19 13 17 23 84 C 
4. Tagiades japetus (Stoll) 07 04 06 10 13 40 UC 
5. Oriens goloides (Moore) 20 15 16 08 21 80 C 
6. Telicota ancilla (Herrich- 
Schaffer) 
12 18 09 16 18 73 C 
7. Pelopidas mathias 
(Fabricius) 
10 09 14 12 17 62 C 
8. Pelopidas assamensis (de 
Niceville) 
04 00 03 07 06 20 UC 
9. Suastus gremius 
(Fabricius) 
00 02 04 06 09 21 UC 
10. Matapa aria (Moore) 12 05 10 13 19 59 C 
11. Iambrix salsala (Moore) 02 04 03 05 06 20 UC 
12. Koruthaialos butleri (de 
Niceville) 
01 00 03 02 03 09 R 
13. Sancus fuligo (Mabille) 09 12 04 11 15 51 C 
Family: Papilionidae 
*14. Papilio polytes (Linn.) 22 33 19 34 42 150 VC 
15 Papilio memnon (Linn.) 13 09 15 21 18 76 C 
16 Papilio protenor (Cramer) 06 01 05 10 07 29 UC 
*17 Papilio demoleus (Linn.) 21 19 34 23 35 132 VC 
18 Papilio helenus (Linn.) 04 07 13 09 06 39 UC 
19. Graphium sarpedon 
(Linn.) 
11 13 09 08 14 55 C 
20. Graphium doson (C. & 
R. Felder) 
04 05 00 07 11 27 UC 
21. Graphium agamemnon 
(Linn.) 
13 08 23 06 18 68 C 
22. Atrophaneura 
aristolochiae (Fabricius) 
01 00 03 01 07 12 R 
Family: Pieridae 
*23. Eurema hacabe (Linn.) 23 32 34 25 42 156 VC 
24. Eurema blanda 
(Boisduval) 
14 23 15 27 21 100 C 
*25. Catopsilia pomona 
(Fabricius) 
13 18 35 32 43 141 VC 
26. Catopsilia pyranthe 
(Linn.) 
12 17 09 14 21 73 C 
27. Colotis etrida (Boisduval) 01 03 02 05 04 15 R
Bora and Meitei 11 
28. Hebomoia glaucippe 
(Linn.) 
12 15 07 16 19 69 C 
29. Appias libythea 
(Fabricius) 
03 00 04 05 08 20 UC 
30. Appias lyncida (Cramer) 11 13 09 15 21 69 C 
*31. Pieris canidia (Sparrman) 21 23 32 39 27 142 VC 
32 Cepora nadina (Lucas) 03 06 09 04 07 29 UC 
33. Delias pasithoe (Linn.) 07 04 02 04 09 26 UC 
34. Delias descombesi 
(Boisduval) 
05 06 09 03 07 30 UC 
35. Leptosia nina (Fabricius) 12 18 14 23 32 99 C 
Family: Lycaenidae 
36. Spalgis epius (Westwood) 00 00 03 05 07 15 R 
37. Arhopala 
pseudocentaurus 
(Dubleday) 
18 14 21 17 23 93 C 
38. Loxura atymnus (Stoll) 04 02 06 02 14 28 UC 
39. Cheritra freja (Fabricius) 12 14 07 13 21 67 C 
40. Hypolycaena erylus 
(Godart) 
07 04 00 05 09 25 UC 
#41. Chliaria othona 
(Hewitson) 
00 01 02 00 01 04 VR 
42. Rapala pheretima 
(Hewitson) 
04 07 05 08 15 39 UC 
43. Rapala iarbus (Fabricius) 12 12 14 18 16 72 C 
44. Rapala manea (Hewitson) 03 00 07 05 04 19 R 
45. Spindasis lohita 
(Horsfield) 
03 04 00 05 04 16 R 
#46. Anthene emolus (Godart) 02 00 00 01 02 05 VR 
47. Castalius rosimon 
(Fabricius) 
09 14 17 20 22 82 C 
48. Leptotes plinius 
(Fabricius) 
11 18 15 22 12 78 C 
49. Prosotas nora (C. 
Felder) 
19 12 13 12 20 76 C 
50. Jamides celeno (Cramer) 21 13 22 20 27 103 C 
51. Lampides boeticus (Linn.) 07 00 08 14 11 40 UC 
52. Zizeeria karsandra 
(Moore) 
15 19 21 18 26 99 C 
53. Pseudozizeeria maha 
(Kollar) 
12 14 09 21 19 75 C 
54. Zizina otis (Fabricius) 21 17 08 13 24 83 C 
55. Neopithecops zalmora 
(Butler) 
27 14 10 12 34 97 C 
56. Euchrysops cnejus 
(Fabricius) 
10 03 01 07 14 35 UC 
*57. Chilades lajus (Stoll) 14 31 15 18 25 103 VC 
58. Zemeros flegyas (Cramer) 19 07 12 14 20 72 C
Bora and Meitei 12 
Family: Nymphalidae 
59. Tirumala limniace 
(Cramer) 
02 04 05 03 09 23 UC 
60. Tirumala septentrionis 
(Butler) 
04 02 00 05 09 20 UC 
61. Danaus chrysippus 
(Linn.) 
12 14 09 21 30 86 C 
62. Danaus genutia (Cramer) 04 07 11 09 12 43 UC 
63. Parantica aglea (Stoll) 12 15 21 13 24 85 C 
64. Euploea Sylvester 
(Fabricius) 
04 04 07 11 13 39 UC 
65. Euploea mulciber 
(Cramer) 
02 08 00 09 12 31 UC 
66. Euploea midamus (Linn,) 01 03 00 05 06 15 R 
67. Euploea core (Cramer) 03 02 07 05 10 27 UC 
#68. Polyura agraria 
(Swinhoe) 
01 00 00 01 02 04 VR 
69. Discophora sondaica 
(Boisduval) 
02 03 05 02 14 26 UC 
#70. Discophora timora 
(Westwood) 
00 00 02 00 01 03 VR 
71. Melanitis leda (Linn.) 10 12 07 23 20 72 C 
72. Melanitis phedima 
(Cramer) 
03 04 03 08 11 29 UC 
#73 Melanitis zitenius 
(Herbst) 
01 03 00 00 00 04 VR 
74. Lethe europa (Fabricius) 06 07 05 04 09 31 UC 
#75. Lethe chandica (Moore) 00 02 00 00 02 04 VR 
76. Elymnias hypermnestra 
(Linn.) 
11 23 17 12 15 78 C 
#77. Mycalesis gotama 
(Moore) 
02 00 00 00 01 03 VR 
*78. Mycalesis perseus 
(Fabricius) 
12 15 23 20 32 102 VC 
79. Mycalesis mineus (Linn.) 19 07 05 12 20 63 C 
80. Ypthima huebneri (Kirby) 17 13 14 21 18 83 C 
*81. Ypthima baldus 
(Fabricius) 
21 25 26 32 34 138 VC 
82. Cethosia biblis (Drury) 02 04 00 03 02 11 R 
83. Argyreus hyperbius 
(Linn.) 
06 08 09 11 07 41 UC 
84. Vagrans egista (Cramer) 12 10 18 21 25 86 C 
*85. Phalanta phalantha 
(Drury) 
21 23 23 29 31 127 VC 
86. Moduza procris (Cramer) 12 09 03 11 07 42 UC 
87. Athyma perius (Linn.) 12 23 14 20 19 88 C 
88. Athyma nefte (Cramer) 12 18 21 12 23 86 C
Bora and Meitei 13 
89. Pantoporia hordonia 
(Stoll) 
03 00 03 02 01 09 R 
90. Neptis hylas (Linn.) 12 12 15 17 20 76 C 
86. Moduza procris (Cramer) 12 09 03 11 07 42 UC 
87. Athyma perius (Linn.) 12 23 14 20 19 88 C 
88. Athyma nefte (Cramer) 12 18 21 12 23 86 C 
90. Neptis hylas (Linn.) 12 12 15 17 20 76 C 
91. Neptis clinia (Moore) 03 01 02 00 04 10 R 
#92. Phaedyma columella 
(Cramer) 
00 00 02 01 00 03 VR 
93. Euthalia aconthea 
(Cramer) 
09 04 11 02 09 35 UC 
94. Tanaecia lepidea (Butler) 12 03 17 12 18 62 UC 
95. Tanaecia jahnu (Moore) 00 03 02 00 05 10 R 
96. Lexias pardalis (Moore) 01 02 03 00 05 11 R 
97. Ariadne merione 
(Cramer) 
11 12 09 09 12 53 UC 
#98. Vanessa indica (Herbst) 00 00 01 00 01 02 VR 
*99. Junonia atlites (Linn.) 21 20 18 20 32 111 VC 
*100 
Junonia almana (Linn.) 23 17 24 19 30 113 VC 
. 
101. Junonia lemonias (Linn.) 12 15 07 18 15 67 C 
102. Junonia hierta (Fabricius) 09 06 12 07 09 43 UC 
103. Junonia iphita (Cramer) 12 13 17 21 26 89 C 
104. Hypolimnas bolina 
(Linn.) 
09 13 14 08 32 76 C 
Total 941 980 1019 1169 1587 5696 
Hesperiidae 
13 
9 
13 
23 
46 
50 
40 
30 
20 
10 
0 
Papilionidae 
Nymphalidae 
Lycaenidae Pieridae 
Fig. 2. Filled Radar showing species diversity of the five families.
Bora and Meitei 14 
Sector 5 
1587 
Sector 4 
1169 
Sector 1 
941 
Sector 2 
980 
Sector 3 
1019 
Fig. 3. Pie Diagram showing no. of individuals recorded in the selected five tea gardens. 
Common Mormon Great Mormon Common Lime 
Papilio polytes (Linn.) Papilio memnon (Linn.) Papilio demoleus (Linn.) 
Common Grass Yellow Red-spot Jazebel Common Pierrot 
Eurema hacabe (Linn.) Delias descombesi (boisduval) Castalius rosimon (Fabricius) 
Common Lascar Grey Count Vagrant 
Pantoporia hordonia (Stoll) Tanaecia lepidea (Butler) Vagrans egista (Cramer) 
Fig. 4. Photographs of some Butterfly fauna recorded within the study areas.
Bora and Meitei 15 
The Government of India under Indian Wildlife 
(Protection) Act, 1972 provided protection to 452 
species of butterfly in three Schedules (out of six) as in 
Schedule I, Part IV, 128 species of butterfly; in 
Schedule II, Part II, 30 species and in Schedule IV 
(Secs. 2, 8, 9, 11 and 61), 19 species listed 
(Anonymous, 2003b). A milestone of the study is the 
recording of the two species Castalius rosimon 
(Common Pierrot) and Pantoporia hordonia (Common 
Lascar) in the study area that are listed in the Indian 
Wildlife Protection Act, 1972 as under Schedule I and 
II (Anonymous, 2006). This two species were 
recorded in all the selected gardens with reasonable 
abundance indicating the superior quality habitat of the 
study areas. The Ministry of Environment and Forests, 
Government of India through various schemes and 
simple methods try to encouraged researchers and 
organization to develop and recreate habitats that might 
play a role in conserving butterfly fauna of India. These 
efforts were already become popular and successful in 
some states of India including Kerala, Tamil Nadu and 
Karnataka. Most tea gardens are governed by a strict 
administration that does not allow illegal anthropogenic 
activities inside the garden areas that fully supports the 
wildlife. From this study, it can be clearly suggested 
that tea gardens can be used as ideal habitats for 
conserving butterfly fauna by introducing appropriate, 
naturally occurring host plants. The photo gallery (Fig. 
4.) provides the photographic proof of our study in the 
proposed study area. 
ACKNOWLEDGEMENTS 
Authors are grateful to the Tea Garden officials and 
staff members for their kind corporation and help 
during the study. 
REFERENCES 
Anonymous (2003b). The Wildlife (Protection) Act, 
1972 (53 of 1972) as amended by the Wildlife 
(Protection) Amendment Act, 2002. Universal 
Law Publishing Co. Pvt. Ltd. 126pp. 
Anonymous (2006). The Wildlife (Protection) Act 
1972. Natraj Publishers. 
Barhaum, K.P., Anderson, D.R. and Cauke, Z.L. (1980- 
1981). Estimation of density from line 
transects sampling of biological population. 
WILD, Monograph No. 72: 515. 
D’Abrera Bernard (1982-86). Butterflies of the Oriental 
Region Part-I-III’. Hill House, Victoria. 
Evans, W.H. (1932). The identfication of Indian 
Butterflies. The Bombay Natural History 
Society, Bombay, India, p.455. 
Eswaran, R. and P. Pramod (2005). Structure of 
butterfly community of Anaikatty hills, 
Western Ghats. Zoo’s print Journal 20(8): 
1939-1942. 
Kehimkar, I. (2008). The Book of Indian Butterflies. 
Bombay Natural History Society and Oxford 
University Press, Mumbai, India, p.497. 
Krishnakumar, N., A. Kumaraguru, K. Thiyagesan and 
S. Asokan (2008). Diversity of papilionid 
butterflies in the Indira Gandhi Wildlife 
Sanctuary, Western Ghats, Southern India. 
Tiger Paper 35: 1-8. 
Morton, A.C. (1984). The effects of making and 
handling on recapture frequencies of 
butterflies. The Biology of Butterflies. 
Academic Press, New York, p.55-58. 
Pyle, R.M. (1984). The Audubon Society Handbook for 
butterfly watchers. Charles Scribner’s Sons, 
New York. 
Talbot, G. (1939). The Fauna of British India including 
Ceylon and Burma. Today & Tomorrows 
Printers and Publishers, New Delhi, p.600. 
Varshney, R.K. (1990). Revised Nomenclature for Taxa 
in Wynther-Blyth’s Book on the Butterflies of 
Indian Region-III. Journal of Bombay natural 
History Society, 87(1): 53-61.

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atanu bora

  • 1. Biological Forum – An International Journal 6(2): 7-15(2014) ISSN No. (Print): 0975-1130 ISSN No. (Online): 2249-3239 Butterfly Fauna (Order: Lepidoptera) in Five Major Tea Gardens of Sivasagar District, Assam, India Atanu Bora* and L.R. Meitei* *Research Scholar, Department of Life Science and Bioinformatics, Assam University, Silchar, Cachar District, Assam, India (Corresponding author: Atanu Bora) (Received 08 July, 2014, Accepted 09 August, 2014) ABSTRACT: The present paper is based on observations and sighting records of butterfly fauna fromMarch 2012 to February 2013 in five major Tea Gardens, Sivasagar District of Assam, India. The district has 119 tea estates which covers an area of 88, 008 hectares of land. The beautiful tea gardens provide a very attractive landscape to the district. Based on the study of butterfly diversity in the study area, a checklist has been prepared. A total of 104 butterfly species belonging to 5 families of order Lepidoptera were recorded during the study period. The family Nymphalidae, represented by 46 species was the most dominant followed by Lycaenidae (23 species), Hesperiidae (13 species), Pieridae (13 species) and Papilionidae (9 species) being the least. From the conservation point of view, the study areas are undisturbed and rich in butterfly fauna. Keywords: Tea gardens, Sivasagar District, Assam, India, butterfly species. INTRODUCTION Geographically, the state of Assam is situated between 24°10’ to 27°58’ N latitude and 89°49’ to 97°26’ E longitude. Sharing its borders with Arunachal Pradesh on the north; Nagaland, Manipur and Arunachal Pradesh on the east; Meghalaya, Mizoram and Tripura on the south and Meghalaya on the west, Assam is located on the north-eastern part of the Indian sub-continent. The state is connected with the rest of the Indian Union by a narrow corridor in West Bengal that runs for 56 Kms. below the foothills of Bhutan and Sikkim. The prime geographical characters that form the topographical features of Assam are the Barak Valley and the River of Brahmaputra. The state occupies a total area of about 78,523 sq km. placed on the foothills of the majestic Himalaya, Assam Forest covers a major part of the total land available in the state. Going by a survey conducted by the Forest Department of Assam Government, in the year 2003, the state possessed a total of 26, 781.91 sq km forest land. Bamboo and timber are the two prime forest products of Assam. The specialty of Assam Climate lies in its highest levels of humidity. Assam is known to have maximum amount of rainfall. The temperatures never go beyond the standard 35° to 38°C. While, the hilly regions of Assam experience a suitable sub-alpine climatic condition, the plain lands of the state go through excessive humid weather. Primarily, the climate of Assam is categorized under two prime heads - rainy season and winter months. The rainy season starts from June while the winter months begin with the onset of October. The minimum temperature which is found in the coldest of months in Assam ranges from 6 to 8°C. Assam is the world's largest tea growing region and not only famous for its quality of tea as well as the natural beauty of the tea plantation area. Beautiful tea estates of Assam cover about 2, 16, 200 hectares of land comprises of more than 100 tea estates. Enormously found mountain region, its greenery and pleasant climate make this location popular not only for its tea, but also for being a popular spot for enjoying eco-vacations. The both sides of the famous river, Brahmaputra, constitute the world's largest Tea growing area. The tea plants are grown in the lowlands of Assam, unlike Darjiling and Nilgiris, which are grown in the highlands. The Assam tea bush grows in a lowland region, in the valley of the Brahmaputra River, an area of clay soil rich in the nutrients of the floodplain. The climate varies between a cool, and winter and hot, humid rainy seasons- the conditions ideal for growing tea. Because of its lengthy growing seasons and generous rainfall of about 250-300 mm (during the monsoon season), Assam is one of the most prolific tea-producing region in the world. This region of India is so famous for its tea plantation that Assam tourism has organized the Assam Tea festival in the month of November every year that makes a totally new experience to enjoy this place.
  • 2. Bora and Meitei 8 MATERIAL AND METHODS Study Area. The present study was conducted to study the diversity of butterfly fauna in five major tea gardens of Sivasager district, Assam, India from March 2012 to February 2013. Sivasagar district is situated in the North-Eastern part of Assam between 94.25° to 95.25° N latitude and 26.45° to 27.15° E longitude. It is placed in 99 meters to 103 meters elevation range above sea level. Fig.1. Location map of Sivasagar District showing study sites.
  • 3. Bora and Meitei 9 The district is surrounded by Lakhimpur and Dibrugarh in the north, Arunachal Pradesh and Dibrugarh in the east, Arunachal Pradesh and Nagaland in the south, Jorhat district of Assam in the west. The Naga Hills lie towards the south, while the Brahmaputra River is on the north. The district is located at Upper Brahmaputra Valley of Agro-climatic zone of the state and occupies a total geographical area of 2668 sq.km. The district is situated in the humid sub-tropical region and characterized by heavy rainfall and high relative humidity above 90%; high temperature up to 38°C is observed in the summer season and comparatively low temperature up to 7°C in winter. The soils of this zone is immature alluvial in char to mature ultisol in the piedmont high and hill areas. The vegetation is mostly tropical evergreen with trees like Hollong, Titachapa, Nahor, Mekai etc. dominating the forest canopy. Sivasagar’s biggest contribution to the world is its tea plantation. There are 119 tea estates in the district which covers an area of 88, 008 hectares. Besides these tea estates, 80 registered small tea growers and 4, 004 small tea growers covers the 5356 hectares of land in this district. The district produces some of the finest and most expensive teas in the world. Tea gardens of the district not only produce economy but also it adds the scenic beauty. The beautiful tea gardens provide a very attractive landscape to the district. The five major tea gardens of the district where the study was conducted are as follows – Sector 1: Maskara Tea Estate, P.O. Rajmai: Total area under tea cover is 44.71 hectares. Sector 2: Bezbaruah Tea Estate, P.O. Sapekhati: Total area under tea cover is 89.43 hectares. Sector 3: Aideobari Tea Estate, P.O. Sonari: Total area under tea cover is 150.65 hectares. Sector 4: Bemolapur Tea Estate, P.O. Borhat: Total area of the estate is 1214 hectares, out of which 527 hectares is under tea cover. Sector 5: Behubor Tea Estate, P.O. Nazira: Total area under tea cover is 533.86 hectares. Taxonomic Study. Field notes, photographs (camera: Nikon d5100) and observations of butterflies were taken for the entire growing season during the day light hours. The population trends of butterflies were monitored for one year using transects counting method (Barhaum et al., 1980). Butterflies were netted only when necessary to prevent the possibility of handling effect (Morton, 1984). Species were noted along with the date, location of capture and any plant association. Other factors noted include the time of day using a twenty-four hour clock and the weather conditions. At each location the same route of inspection was followed each time to reduce the number of variables presents (Pyle, 1984) and to avoid any personal difference all the counts were made by the same person. An effort has been made to use the latest nomenclature and common names as far as possible as per Evan (1932), D’ Abrera (1982-1986), Varshney (1990) and Kehimkar (2008). The relative abundance or say status of individual species is categorized within the tea gardens as “Very Rare” (VR) when recorded rarely; “Rare” (R) when recorded occasionally; “Uncommon” (UC) when recorded frequently; “Common” (C) when recorded regularly; “Very Common” (VC) when recorded regularly in large numbers. RESULT AND DISCUSSION During the study, a total of 104 species belonging to 72 genera under 5 families were recorded from the selected five major tea garden areas (Table 1). The family Nymphalidae showed the maximum species richness, comprising of 27 genera and 46 species, followed by Lycaenidae (21 genera, 23 species), Hesperiidae (12 genera, 13 species), Pieridae (9 genera, 13 species) and Papilionidae (3 genera, 9 species) being the least (Fig. 2). Abundance showed that out of the 104 butterfly species recorded, 33 are uncommon, 39 are common, 11 are very common, 12 are rare and 9 are very rare to the study area. A total of 5696 individuals were recorded from the five tea gardens, of which the Sector 5 representing the Behubor Tea Estate contributing 1587 individuals was dominant while the Sector 1 representing the Maskara Tea Estate with 941 individuals was the least (Fig. 3). Eurema hecabe (Linn.) was the most dominant species of butterfly in terms of number of individuals (156) followed by Papilio polytes (Linn.) (150), Pieris canidia (Sparrman) (142), Catopsilia pomona (Fabricius) (141), Ypthima baldus (Fabricius) (138) and 6 other species in the study area (Table 1, *Marked Asterisks). Discophora timora (Westwood) and Mycalesis gotama (Moore) (3 individuals each) were the rarest species followed by Chliaria othona (Hewitson) (4), Polyura agraria (Swinhoe) (4) and 5 other species (Table 1, #Marked Asterisks). Results suggested that the family Nymaphalidae with 27 genera and 46 species was the most dominant in the study area. Members of the Nymphalidae were always dominant in the tropical region because most of the species are polyphagous in nature, consequently helping them to live in all the habitats. Additionally, many species of this family are strong, active fliers that might help them in searching for resources in large areas (Eswaran and Pramod 2005; Krishna Kumar et al. 2007). A high proportion of nymphalid species thus clearly indicates high host plant richness in the study areas.
  • 4. Bora and Meitei 10 Table 1: Checklist of Butterflies and their abundance recorded in selected five major Tea Gardens, Sivasagar District, Assam. Sl. No. Scientific Name Sector 1 Sector 2 Sector 3 Sector 4 Sector 5 Total Relative Abundance Family: Hesperiidae 1. Bibasis oedipodea (Swainson) 05 04 02 00 06 17 UC 2. Hasora chromus (Cramer) 02 06 02 02 05 17 UC 3. Pseudocoladenia dan (Fabricius) 12 19 13 17 23 84 C 4. Tagiades japetus (Stoll) 07 04 06 10 13 40 UC 5. Oriens goloides (Moore) 20 15 16 08 21 80 C 6. Telicota ancilla (Herrich- Schaffer) 12 18 09 16 18 73 C 7. Pelopidas mathias (Fabricius) 10 09 14 12 17 62 C 8. Pelopidas assamensis (de Niceville) 04 00 03 07 06 20 UC 9. Suastus gremius (Fabricius) 00 02 04 06 09 21 UC 10. Matapa aria (Moore) 12 05 10 13 19 59 C 11. Iambrix salsala (Moore) 02 04 03 05 06 20 UC 12. Koruthaialos butleri (de Niceville) 01 00 03 02 03 09 R 13. Sancus fuligo (Mabille) 09 12 04 11 15 51 C Family: Papilionidae *14. Papilio polytes (Linn.) 22 33 19 34 42 150 VC 15 Papilio memnon (Linn.) 13 09 15 21 18 76 C 16 Papilio protenor (Cramer) 06 01 05 10 07 29 UC *17 Papilio demoleus (Linn.) 21 19 34 23 35 132 VC 18 Papilio helenus (Linn.) 04 07 13 09 06 39 UC 19. Graphium sarpedon (Linn.) 11 13 09 08 14 55 C 20. Graphium doson (C. & R. Felder) 04 05 00 07 11 27 UC 21. Graphium agamemnon (Linn.) 13 08 23 06 18 68 C 22. Atrophaneura aristolochiae (Fabricius) 01 00 03 01 07 12 R Family: Pieridae *23. Eurema hacabe (Linn.) 23 32 34 25 42 156 VC 24. Eurema blanda (Boisduval) 14 23 15 27 21 100 C *25. Catopsilia pomona (Fabricius) 13 18 35 32 43 141 VC 26. Catopsilia pyranthe (Linn.) 12 17 09 14 21 73 C 27. Colotis etrida (Boisduval) 01 03 02 05 04 15 R
  • 5. Bora and Meitei 11 28. Hebomoia glaucippe (Linn.) 12 15 07 16 19 69 C 29. Appias libythea (Fabricius) 03 00 04 05 08 20 UC 30. Appias lyncida (Cramer) 11 13 09 15 21 69 C *31. Pieris canidia (Sparrman) 21 23 32 39 27 142 VC 32 Cepora nadina (Lucas) 03 06 09 04 07 29 UC 33. Delias pasithoe (Linn.) 07 04 02 04 09 26 UC 34. Delias descombesi (Boisduval) 05 06 09 03 07 30 UC 35. Leptosia nina (Fabricius) 12 18 14 23 32 99 C Family: Lycaenidae 36. Spalgis epius (Westwood) 00 00 03 05 07 15 R 37. Arhopala pseudocentaurus (Dubleday) 18 14 21 17 23 93 C 38. Loxura atymnus (Stoll) 04 02 06 02 14 28 UC 39. Cheritra freja (Fabricius) 12 14 07 13 21 67 C 40. Hypolycaena erylus (Godart) 07 04 00 05 09 25 UC #41. Chliaria othona (Hewitson) 00 01 02 00 01 04 VR 42. Rapala pheretima (Hewitson) 04 07 05 08 15 39 UC 43. Rapala iarbus (Fabricius) 12 12 14 18 16 72 C 44. Rapala manea (Hewitson) 03 00 07 05 04 19 R 45. Spindasis lohita (Horsfield) 03 04 00 05 04 16 R #46. Anthene emolus (Godart) 02 00 00 01 02 05 VR 47. Castalius rosimon (Fabricius) 09 14 17 20 22 82 C 48. Leptotes plinius (Fabricius) 11 18 15 22 12 78 C 49. Prosotas nora (C. Felder) 19 12 13 12 20 76 C 50. Jamides celeno (Cramer) 21 13 22 20 27 103 C 51. Lampides boeticus (Linn.) 07 00 08 14 11 40 UC 52. Zizeeria karsandra (Moore) 15 19 21 18 26 99 C 53. Pseudozizeeria maha (Kollar) 12 14 09 21 19 75 C 54. Zizina otis (Fabricius) 21 17 08 13 24 83 C 55. Neopithecops zalmora (Butler) 27 14 10 12 34 97 C 56. Euchrysops cnejus (Fabricius) 10 03 01 07 14 35 UC *57. Chilades lajus (Stoll) 14 31 15 18 25 103 VC 58. Zemeros flegyas (Cramer) 19 07 12 14 20 72 C
  • 6. Bora and Meitei 12 Family: Nymphalidae 59. Tirumala limniace (Cramer) 02 04 05 03 09 23 UC 60. Tirumala septentrionis (Butler) 04 02 00 05 09 20 UC 61. Danaus chrysippus (Linn.) 12 14 09 21 30 86 C 62. Danaus genutia (Cramer) 04 07 11 09 12 43 UC 63. Parantica aglea (Stoll) 12 15 21 13 24 85 C 64. Euploea Sylvester (Fabricius) 04 04 07 11 13 39 UC 65. Euploea mulciber (Cramer) 02 08 00 09 12 31 UC 66. Euploea midamus (Linn,) 01 03 00 05 06 15 R 67. Euploea core (Cramer) 03 02 07 05 10 27 UC #68. Polyura agraria (Swinhoe) 01 00 00 01 02 04 VR 69. Discophora sondaica (Boisduval) 02 03 05 02 14 26 UC #70. Discophora timora (Westwood) 00 00 02 00 01 03 VR 71. Melanitis leda (Linn.) 10 12 07 23 20 72 C 72. Melanitis phedima (Cramer) 03 04 03 08 11 29 UC #73 Melanitis zitenius (Herbst) 01 03 00 00 00 04 VR 74. Lethe europa (Fabricius) 06 07 05 04 09 31 UC #75. Lethe chandica (Moore) 00 02 00 00 02 04 VR 76. Elymnias hypermnestra (Linn.) 11 23 17 12 15 78 C #77. Mycalesis gotama (Moore) 02 00 00 00 01 03 VR *78. Mycalesis perseus (Fabricius) 12 15 23 20 32 102 VC 79. Mycalesis mineus (Linn.) 19 07 05 12 20 63 C 80. Ypthima huebneri (Kirby) 17 13 14 21 18 83 C *81. Ypthima baldus (Fabricius) 21 25 26 32 34 138 VC 82. Cethosia biblis (Drury) 02 04 00 03 02 11 R 83. Argyreus hyperbius (Linn.) 06 08 09 11 07 41 UC 84. Vagrans egista (Cramer) 12 10 18 21 25 86 C *85. Phalanta phalantha (Drury) 21 23 23 29 31 127 VC 86. Moduza procris (Cramer) 12 09 03 11 07 42 UC 87. Athyma perius (Linn.) 12 23 14 20 19 88 C 88. Athyma nefte (Cramer) 12 18 21 12 23 86 C
  • 7. Bora and Meitei 13 89. Pantoporia hordonia (Stoll) 03 00 03 02 01 09 R 90. Neptis hylas (Linn.) 12 12 15 17 20 76 C 86. Moduza procris (Cramer) 12 09 03 11 07 42 UC 87. Athyma perius (Linn.) 12 23 14 20 19 88 C 88. Athyma nefte (Cramer) 12 18 21 12 23 86 C 90. Neptis hylas (Linn.) 12 12 15 17 20 76 C 91. Neptis clinia (Moore) 03 01 02 00 04 10 R #92. Phaedyma columella (Cramer) 00 00 02 01 00 03 VR 93. Euthalia aconthea (Cramer) 09 04 11 02 09 35 UC 94. Tanaecia lepidea (Butler) 12 03 17 12 18 62 UC 95. Tanaecia jahnu (Moore) 00 03 02 00 05 10 R 96. Lexias pardalis (Moore) 01 02 03 00 05 11 R 97. Ariadne merione (Cramer) 11 12 09 09 12 53 UC #98. Vanessa indica (Herbst) 00 00 01 00 01 02 VR *99. Junonia atlites (Linn.) 21 20 18 20 32 111 VC *100 Junonia almana (Linn.) 23 17 24 19 30 113 VC . 101. Junonia lemonias (Linn.) 12 15 07 18 15 67 C 102. Junonia hierta (Fabricius) 09 06 12 07 09 43 UC 103. Junonia iphita (Cramer) 12 13 17 21 26 89 C 104. Hypolimnas bolina (Linn.) 09 13 14 08 32 76 C Total 941 980 1019 1169 1587 5696 Hesperiidae 13 9 13 23 46 50 40 30 20 10 0 Papilionidae Nymphalidae Lycaenidae Pieridae Fig. 2. Filled Radar showing species diversity of the five families.
  • 8. Bora and Meitei 14 Sector 5 1587 Sector 4 1169 Sector 1 941 Sector 2 980 Sector 3 1019 Fig. 3. Pie Diagram showing no. of individuals recorded in the selected five tea gardens. Common Mormon Great Mormon Common Lime Papilio polytes (Linn.) Papilio memnon (Linn.) Papilio demoleus (Linn.) Common Grass Yellow Red-spot Jazebel Common Pierrot Eurema hacabe (Linn.) Delias descombesi (boisduval) Castalius rosimon (Fabricius) Common Lascar Grey Count Vagrant Pantoporia hordonia (Stoll) Tanaecia lepidea (Butler) Vagrans egista (Cramer) Fig. 4. Photographs of some Butterfly fauna recorded within the study areas.
  • 9. Bora and Meitei 15 The Government of India under Indian Wildlife (Protection) Act, 1972 provided protection to 452 species of butterfly in three Schedules (out of six) as in Schedule I, Part IV, 128 species of butterfly; in Schedule II, Part II, 30 species and in Schedule IV (Secs. 2, 8, 9, 11 and 61), 19 species listed (Anonymous, 2003b). A milestone of the study is the recording of the two species Castalius rosimon (Common Pierrot) and Pantoporia hordonia (Common Lascar) in the study area that are listed in the Indian Wildlife Protection Act, 1972 as under Schedule I and II (Anonymous, 2006). This two species were recorded in all the selected gardens with reasonable abundance indicating the superior quality habitat of the study areas. The Ministry of Environment and Forests, Government of India through various schemes and simple methods try to encouraged researchers and organization to develop and recreate habitats that might play a role in conserving butterfly fauna of India. These efforts were already become popular and successful in some states of India including Kerala, Tamil Nadu and Karnataka. Most tea gardens are governed by a strict administration that does not allow illegal anthropogenic activities inside the garden areas that fully supports the wildlife. From this study, it can be clearly suggested that tea gardens can be used as ideal habitats for conserving butterfly fauna by introducing appropriate, naturally occurring host plants. The photo gallery (Fig. 4.) provides the photographic proof of our study in the proposed study area. ACKNOWLEDGEMENTS Authors are grateful to the Tea Garden officials and staff members for their kind corporation and help during the study. REFERENCES Anonymous (2003b). The Wildlife (Protection) Act, 1972 (53 of 1972) as amended by the Wildlife (Protection) Amendment Act, 2002. Universal Law Publishing Co. Pvt. Ltd. 126pp. Anonymous (2006). The Wildlife (Protection) Act 1972. Natraj Publishers. Barhaum, K.P., Anderson, D.R. and Cauke, Z.L. (1980- 1981). Estimation of density from line transects sampling of biological population. WILD, Monograph No. 72: 515. D’Abrera Bernard (1982-86). Butterflies of the Oriental Region Part-I-III’. Hill House, Victoria. Evans, W.H. (1932). The identfication of Indian Butterflies. The Bombay Natural History Society, Bombay, India, p.455. Eswaran, R. and P. Pramod (2005). Structure of butterfly community of Anaikatty hills, Western Ghats. Zoo’s print Journal 20(8): 1939-1942. Kehimkar, I. (2008). The Book of Indian Butterflies. Bombay Natural History Society and Oxford University Press, Mumbai, India, p.497. Krishnakumar, N., A. Kumaraguru, K. Thiyagesan and S. Asokan (2008). Diversity of papilionid butterflies in the Indira Gandhi Wildlife Sanctuary, Western Ghats, Southern India. Tiger Paper 35: 1-8. Morton, A.C. (1984). The effects of making and handling on recapture frequencies of butterflies. The Biology of Butterflies. Academic Press, New York, p.55-58. Pyle, R.M. (1984). The Audubon Society Handbook for butterfly watchers. Charles Scribner’s Sons, New York. Talbot, G. (1939). The Fauna of British India including Ceylon and Burma. Today & Tomorrows Printers and Publishers, New Delhi, p.600. Varshney, R.K. (1990). Revised Nomenclature for Taxa in Wynther-Blyth’s Book on the Butterflies of Indian Region-III. Journal of Bombay natural History Society, 87(1): 53-61.