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International Journal of
eISSN: 2574-9862

Avian & Wildlife Biology

Research Article Volume 3 Issue 3

Avian and wildlife diversity in the area of bauxite mining near lamba village, Dwarka in the state of Gujarat, India

Ashok K Rathoure

Ashok K Rathoure, Ecology & Biodiversity Expert, Ecosystem Resource Management Pvt. Ltd., Hardoi-241001 (UP), India

Correspondence: Ashok K Rathoure, Ecology & Biodiversity Expert, Ecosystem Resource Management Pvt. Ltd., Hardoi-241001 (UP), India, Tel 9194 5050 1471

Received: May 11, 2018 | Published: June 4, 2018

Citation: Rathoure Ak. Avian and wildlife diversity in the area of bauxite mining near lamba village, Dwarka in the state of Gujarat, India. Int J Avian & Wildlife Biol. 2018;3(3):225-229. DOI: 10.15406/ijawb.2018.03.00090

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Abstract

The bauxite is the primary ore of aluminum. Almost all of the aluminum that has ever been produced has been extracted from bauxite. The area in question is rich in bauxite and lime. The mining activity increasing day by day which hinder the movement of wildlife especially birds. The area of bauxite mining is proximity to sea shore and major creek. In this study, 38 birds species (1 species protected under schedule –1 as per Indian Wildlife Protection Act 1972), 10 species of reptiles, 5 species of mammals, 13 species of marine fishes were observed.

Keywords: bauxite mining, core zone, buffer zone, mining, avian–biodiversity

Introduction

The avian and wildlife biodiversity of an area depends on several factors of biotic and abiotic components. The coastal areas are rich in avian biodiversity especially sea birds. The mining activity hinders the movement of avian fauna. The bauxite mining activity increasing as demand increased of bauxite for the industrial use. The unorganized and unscientific industrial activities lead the deterioration of abiotic components which affect biotic components. Study area (Figure 1) comprises of 30% Sea, 29% cropping (dominant crop is ground nut), 9% Grassland, 7% fallow land, 5% stone (mainly bauxite), 2% Forest area, 1% human settlement and other area which is dry. The main activity in this area is mining of bauxite mineral as the area is rich in bauxite and lime.

Figure 1 Study area Map.

Methodology

The detailed method and parameters covered for the said study has been highlighted in Table 1. The study area comprises of 8 villages viz. Lamba, Maleta, Navedra, Jodhpar, Gangdi, Satapar, Chachlana, Jamdevliya (Figure 1). Secondary sources and literature was reviewed to identify the representative variety of vulnerable species, inhabitants and ecological groups listed by IUCN, WCMC, ZSI, BSI and Indian Wild life Protection Act, 1972.1–26 The status of individual species was assessed using the revised IUCN/SSC category system (Table 1) (Figure 1).27–36

Data

Mode of Data Collection

Parameters Monitored

Remarks

Primary data
collection

By Field Survey

–Reptiles,
–Amphibians,
–Birds,
–Fresh water fishes
–Mammals,
–Butterflies.
Rare and Endangered fauna in the study area,
Endemic fauna in the study area,
Wild life and their conservation importance in the study area.

Random survey, opportunistic observations, diurnal bird observation, active search for reptiles, faunal habitat assessment, active search for microhabitat, scats, foot prints, animal call, pug marks, debarking sign, Nesting, Claws, Dung, etc. and information from local villagers.12–26

Secondary
data collection

Forest Division
Data of Fisheries department.
Literature like research papers, books published by research/academic institutions.

Interpretation of secondary data for Ecological Sensitive Areas such as national forests, wild life sanctuaries, lakes, ravines, hills, hillocks and reserve forest, importance etc.

The status of individual species was assessed using the revised IUCN/SSC category system.27–36

Table 1 Mode of Data collection and Parameters considered during the Survey

Results and discussion

As per the map prepared by National Bureau of Soil Survey & Land Use Planning (NBSS&LUP), the study area fall under Central Malwa Highlands, Gujarat Plains and Kathiawar Peninsula which represents hot semi–arid eco–region with medium and deep black soils favorable for millets, wheat, pulses. In this area the agro–biodiversity should be promoted. As per the personal observation recorded (Figure 2), the area has scarcity of drinking water, the vegetation in the area is sparsely distributed, road side plantation and natural creek (mangrove) making the area green for avian wildlife.

Figure 2 Glimpses of Local information and Confirmation from villagers.

Status of the forest

The forest areas of Gujarat are unevenly distributed. The major concentration of forests is found all along the eastern border of the state and the hilly portion of Saurashtra. The wide variations in Geophysical and Eco–climatic conditions ranging from hot saline deserts to humid hilly tracts and from coast to high hills have resulted in to formation of various types of forest. No forest land is involved within the mine lease area; however it is present in the study area. On the basis of forest classification by Champion and Seth 1968, tropical dry deciduous forest exists in the study area. In this type of forest vegetation developed due to they have long dry seasons which last several months and vary with geographic location. The common trees are the teak and a variety of acacia. However, vegetation in core are of mine is very sparsely distributed. As per revenue record and toposheet (SOI), there is a reserved forest (open scrub) for stony waste area. This can be classified under open scrub. This is open and having no vegetation currently, reserved for bauxite mineral.

Avian biodiversity

The 38 avian species were encountered during the survey. The most commonly spotted bird species of this area were Accipiter badius (Gmelin, 1788), Acridotheres ginginianus (Latham 1790), Bubulcus ibis (Linnaeus, 1758), Dicrurus macrocercus (Vieillot, 1817), Merops leschenaulti (Vieillot, 1817), Phalacrocorax fuscicollis (Stephens, 1826), Psittacula krameri (Scopoli, 1769), Vanellus indicus (Boddaert, 1783), Muscicapa striata (Pallas, 1764). Water birds are very common as creek and sea shore line is the major part falls under study area. The Indian Peafowl was observed which is listed as schedule –I as per IWPA, 1972 and others listed as schedule IV as per IWPA, 1972. Total 38 avian species encountered during the study listed in Table 2.

SNO

Family

Common Name

Scientific Name

Schedule/IUCN

Status

1

Accipitridae

Shikra

Accipiter badius (Gmelin, 1788)

Schedule IV

R

Imperial Eagle

Aquila heliaca (Saigny, 1809)

Vulnerable

R

Black–winged Kite

Elanus caeruleus(Desfontaines, 1789)

Schedule IV

R

2

Alaudidae

Oriental Sky Lark

Alauda gulgula (Franklin, 1831)

Schedule IV

M

3

Alcedinidae

White–throated Kingfisher

Halcyon smyrnensis (Linnaeus, 1758)

Schedule IV

R

4

Ardeidae

Indian pond heron

Ardeola grayii (Sykes, 1832)

Schedule IV

R

Cattle Egret

Bubulcus ibis (Linnaeus, 1758)

Schedule IV

RM

Little Egret

Egretta garzetta (Linnaeus, 1766)

Schedule IV

R

5

Charadriidae

Lapwing

Vanellus indicus (Boddaert, 1783)

Schedule IV

R

6

Ciconiidae

Painted Stork

Mycteria leucocephala (Pennant, 1769)

Schedule IV

RM

7

Columbidae

Eurasian Collared–Dove

Streptopelia decaocto (Frivaldszky, 1838)

Schedule IV

R

Rufous Turtle
Dove

Streptopelia orientali  (Latham, 1790)

Schedule IV

RM

8

Coraciidae

Indian Roller

Coracias benghalensis (Linnaeus, 1758)

LC

R

9

Cuculidae

Crow–Pheasant

Centropus sinensis (Stephens, 1815)

LC

R

Blue Rock Pigeon

Columba livia (Gmelin, 1789)

LC

R

10

Dicruridae

Black drongo

Dicrurus macrocercus (Vieillot, 1817)

LC

R

11

Laniidae

Great Grey Shrike

Lanius excubitor (Linnaeus, 1758)

Schedule IV

RM

12

Laridae

Little Tern

Sternula albifrons(Pallas, 1764)

LC

R

13

Leiotrichidae

Common Babbler

Turdoides caudatus (Dumont, 1823)

Schedule IV

R

14

Meropidae

Chestnut–headed
Bee–eater

Merops leschenaulti(Vieillot, 1817)

LC

R

15

Motacillidae

Yellow Wagtail

Motacilla flava(Linnaeus, 1758)

Schedule IV

RM

16

Muscicapidae

Spotted Flycatcher

Muscicapa striata(Pallas, 1764)

Schedule IV

R

17

Nectariniidae

Purple Sunbird

Nectarinia asiatica(Latham, 1790)

Schedule IV

R

18

Passeridae

House sparrow

Passer domesticus(Linnaeus, 1758)

LC

R

19

Phalacrocoracidae

Cormorant

Phalacrocorax fuscicollis(Stephens, 1826)

Schedule IV

R

Little Cormorant

Phalacrocorax niger(Vieillot, 1817)

Schedule IV

RM

20

Phasianidae

Indian Peafowl

Pavo cristatus(Linnaeus, 1758)

Schedule I

R

21

Phoenicopteridae

Lesser Flamingo

Phoenicopterus minor(Geoffroy Saint–Hilaire, 1798)

Schedule IV

RM

22

Ploceidae

Baya weaver

Ploceus philippinus(Linnaeus, 1766)

Schedule IV

R

23

Podicipedidae

Little Grebe

Tachybaptus ruficollis(Pallas, 1764)

Schedule IV

R

24

Psittacidae

Rose–ringed Parakeet

Psittacula krameri(Scopoli, 1769)

Schedule IV

R

25

Rallidae

White–breasted Water hen

Amaurornis phoenicurus (Pennant, 1769)

Schedule IV

R

Coot

Fulica atra(Linnaeus, 1758)

Schedule IV

R

26

Scolopacidae

Ruff

Philomachus pugnax(Linnaeus, 1758)

LC

R

27

Sturnidae

Bank Myna

Acridotheres ginginianus(Latham 1790)

Schedule IV

R

28

Threskiornithidae

Eurasian Spoonbill

Platalea leucorodia(Linnaeus, 1758)

Schedule IV

P

Red–naped ibis

Pseudibis papillosa(Temminck, 1824)

Schedule IV

R

Black headed ibis

Throskiornis
Melanocephalus(Latham, 1790)

Schedule IV

M

Table 2 Avian Biodiversity in the area

R–Resident, M– Migratory, RM – Resident & Migratory

Wildlife: In amphibian group, the toads were sighted during the study period. In the reptile group, Calotes versicolor (Cuvier, 1817), Hemidactylus flaviviridis (Ruppell, 1835), Sitana ponticeriana (Cuvier, 1817), Bungarus caeruleus (Schneider, 1801) etc. were observed in the region is given in the Table 3. In the mammals; Funambulus pennantii (Wroughton, 1905), Pteropus giganteus (Brünnich, 1782), Lepus nigricollis (F. Cuvier, 1823), Boselaphus tragocamelus (Pallas, 1766) and Herpestes javanicus (Geoffory Saint–Hilaire, 1818) were observed in the study area are listed in the Table 4. The marine fishes Pampus chinensis (Bonaparte, 1834), Penaeus indicus (Milne–Edwards, 1837), Mugil cephalus (Linnaeus, 1758), Mugil dussumieri (Linnaeus, 1758), Harpodon neherius (Hamilton, 1822), Polynemus indicus (Linnaeus, 1758), Tenualosa ilisha (Hamilton, 1822) etc. are encountered in the coastal area (Figure 3) listed in Table 5.

Figure 3 Marine view at Sea Shore near the Lamba Village.

SNO

Family

Common Name

Scientific Name

Schedule as per 1972

1

Agamidae

Common Garden Lizard

Calotes versicolor(Cuvier, 1817)

Not listed

Fan–Throated Lizard

Sitana ponticeriana(Cuvier, 1817)

Not listed

2

Agamidiae

Roux's Forest Lizard

Calotes rouxii(Dumeril and Bibron, 1837)

Not listed

3

Chamaeleonidae

Indian Chameleon

Chameleon zeylanicus(Rafinesque, 1815)

Not listed

4

Colubridae

Checkered Keelback

Xenochrophis piscator(Schneider, 1799)

Schedule II

5

Elapidae

Indian Cobra

Naja naja(Linnaeus, 1758)

Schedule II

Common Indian Krait

Bungarus caeruleus(Schneider, 1801)

Schedule II

6

Gekkonidae

House  Gecko

Hemidactylus flaviviridis (Ruppell, 1835)

Not listed

7

Viperidae

Indian Saw Scaled Viper

Echis carinatus(Schneider, 1801)

Not listed

8

Russell's Viper

Daboia russelli(Shaw & Nodder, 1797)

Schedule II

Table 3 List of Reptiles in the Study Area

SNO

Family

Common Name

Scientific Name

Status as per IWPA 1972/IUCN

1

Antilopinae

Blue Bull

Boselaphus tragocamelus(Pallas, 1766)

Schedule III

2

Herpestidae

Small Asian mongoose

Herpestes javanicus (Geoffory Saint–Hilaire, 1818)

Schedule II

3

Leporidae

Indian Hare

Lepus nigricollis (F. Cuvier, 1823)

Schedule IV

4

Pteropodidae

Indian flying fox/Fruit bat

Pteropus giganteus(Brünnich, 1782)

LC

5

Sciuridae

Five striped Palm Squirrel

Funambulus pennantii(Wroughton, 1905)

Schedule IV

Table 4 Mammals in Study Area

SNO

Family

Common Name

Scientific Name

1

Clupeidae

Hilsa shad

Tenualosa ilisha (Hamilton, 1822)

2

Mugilidae

Blue Spot Grey Mullet

Valamugil seheli*(Forsskal, 1775)

3

Grey Mullet

Mugil cephalus (Linnaeus, 1758)

4

Mullet

Mugil dussumieri (Linnaeus, 1758)

5

Penaeidae

Indian Prawn

Penaeus indicus (Milne–Edwards, 1837)

6

Polynemidae

Thread Fin

Polynemus indicus (Linnaeus, 1758)

7

Stromateidae

Pomfret

Pampus chinensis(Bonaparte, 1834)

8

Synodontidae

Bombay Duck (Bumla)

Harpodon neherius(Hamilton, 1822)

9

Sciaenidae

Jewfish

Pseudosciaena amblyceps  (Bleeker, 1863)

10

Argyrosomus japonicus (Temminck & Schlegel, 1844)

11

 

 

Protonibea diacanthus (Lacepede, 1802)

Table 5 List of Marine Fish
*not seen directly

Domestic animals: Camel, Bull, Buffalo, Sheep, Cow, Goat, etc.

Insects: like Wasps, Honeybees and Signature spider was also recorded (Figure 2) (Figure 3).

RET species: The IUCN Red List is the world's most comprehensive inventory of the global conservation status of plant and animal species. It uses a set of criteria to evaluate the extinction risk of thousands of species and subspecies. Among the birds in the study area, Pea fowl (Pavo cristatus) is included in schedule I of Wild life protection Act (1972), while many other birds are included in schedule IV. Among the reptiles Xenochrophis piscator (Schneider, 1799), Naja naja (Linnaeus, 1758), Bungarus caeruleus (Schneider, 1801) and Daboia russelli (Shaw & Nodder, 1797) provided protection as per Schedule–II of Indian Wild life Protection Act, (1972). In the mammal group, Herpestes javanicus (Geoffory Saint–Hilaire, 1818) is protected under schedule–II while others are not covered under schedule–I or II as per Indian Wild life Protection Act, (1972).

Conclusion

Study area has 30% sea shore and 70% terrestrial. No any major forest observed in the study area, the wild life distribution is meager. The wildlife can sustain when human influence will be minimized and agro–forestry will be encouraged. An urgent need to protect agro–biodiversity of the area by using good practice in bauxite mining such as controlled wet blasting, 5m high boundary on periphery of mining area; regular water sprinkling and manual mining instead of mechanized mining, plantation over benches, grooves development, rainwater harvesting and its use in irrigation and restoration of mine pits. The effective plantation should be done in 3 tier green belt development to protect the avian biodiversity of the area.

Acknowledgements

None.

Conflict of interest

Author declared that he has no conflict of interest.

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