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International Journal of
eISSN: 2574-9862

Avian & Wildlife Biology

Research Article Volume 4 Issue 1

Colonial nesting of Asian openbill storks (Anastomus oscitans) in Nandankanan Wildlife Sanctuary, Odisha

RK Mohapatra,1 BP Panda,2 MK Panda,1 S Purohit,3 SP Parida,4 KL Purohit,1 JK Das,1 HS Upadhyaya1

1Nandankanan Biological Park, Bhubaneswar –754005, Odisha, India
2ITER, Siksha ‘O’ Anusandhan Deemed University, Bhubaneswar –751030, Odisha, India
3DBCNR, Central University of Orissa, Koraput–764021, Odisha, India
4Dept. of Zoology, School of Applied Sciences, Centurion University, Bhubaneswar– 752050, Odisha, India

Correspondence: Rajesh Kumar Mohapatra, Nandankanan Biological Park, Odisha, India

Received: January 10, 2019 | Published: February 8, 2019

Citation: Mohapatra RK, Panda BP, Panda MK, et al. Colonial nesting of Asian openbill storks (Anastomus oscitans) in Nandankanan Wildlife Sanctuary, Odisha. Int J Avian & Wildlife Biol. 2019;4(1):14-17. DOI: 10.15406/ijawb.2019.04.00145

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Abstract

A field study on nesting habits of Asian openbill stork (Anastomus oscitans) was conducted during breeding seasons of 2015 and 2018 at Nandankanan Wildlife Sanctuary, Odisha, India. Observations revealed the stocks arrived for nesting in July and most left December. The details of nest and nesting habits were reported.

Introduction

Asian openbill storks Anastomus oscitans (AOS) are the smallest among the nine stork species found in India.1,2 They are pale grey storks with black scapulars and reimages, black tail, short reddish legs and a swollen looking bill with a narrow gap between mandibles.1 Adult birds have a prominent gap between down–curved upper and recurved lower mandible as an adaptation for grasping snails which is their main prey. However young birds are born without gap in the bill.3 They are widely distributed in the plains and the peninsula of the Indian subcontinent.1,4 Although mostly resident within their ranges, these birds cover long distances in response to weather suitability and food availability for overwintering and breeding. They breed during the monsoon between July and September.5 Previous observations have also reported their congregation in nesting colonies with the onset of south–west monsoon from mid June to January.6–8 Colonial nesting site of AOS at Nandankanan Wildlife Sanctuary (NWS) is considered as second largest heronry of the state Odisha, eastern India with nesting report since 1999. But, information and published literatures on the nesting habits, population trend and habitat preference of AOS at NWS are inadequate and inconsistent. The present communication intended to report the details of colonial nesting habits of these storks at NWS.

Material and methods

The study was carried out between June, 2015 and December, 2018 at Nandankanan Wildlife Sanctuary (20°23’08” to 20°24’10”N and 85°48’09” to 85°48’13” E) in the state Odisha, eastern India (Figure 1). The sanctuary spreads over an area of 4.37 sq. km. and has wetland areas more than 1.01 sq. km, which provides a suitable feeding and breeding habitat for many migratory and resident birds including AOS. The sanctuary enjoys a moderately hot humid climate around 30ºC with annual average rainfall of 1350mm. The vegetation is of moist mixed deciduous type.9 The natural forest areas of Nandankanan is home to a rich assemblage of free–living wild animals including 13 species of mammals, 15 species of reptiles, 123 species of birds, 20 species of amphibians, 85 species of butterflies and 51 species of spiders.1013 The documented bird species of the sanctuary includes two species of storks, namely painted stork and Asian openbill stork.

Figure 1 AOS nesting site in Nandankanan Wildlife Sanctuary, Odisha, India.

Field observations on nesting colonies carried out ad libitum from June to December every year. Colony is defined as a group of storks nesting on a contiguous canopy that may have had more than one tree. Observations were made with the naked eye or with 10 x binoculars during day time only. A detailed census of nesting colonies were carried out during first week of October every year. Nesting trees were identified following Panda and Panda.9 Occupied nests were determined by presence of adult storks and/or their egg or chicks. Information like number of nests on each tree, species of nesting tree and number of storks present on the nests was collected during first week of October every year with minimal disturbances to the nesting storks. To gather information regarding nest characteristic including size, depth and height from the ground we measured 50 apparently intact abandoned nests (after fledglings are fledged out of the nests) during 3rd week of December, 2018.

Observations

The species usually form monospecific colonies with an affinity to nest on the upper and upper middle canopy. The colonial nesting recorded in 20 species of trees with maximum number of nests with Pterospermium hyaeneanum tree (Table 1). Other important nesting tree species are Ficus bengalensis, Streblus asper, Aegle marmelus, Syzyjium cumini, Putranjiba rosburghii, Strychnos noxvomica, Melia azadirach, Cassia fistula etc. Nests are constructed at 4.57m–10.67m high from ground. The diameter of the nest varies from 30–61cm and with 20–36cm high nesting materials. The nests are shallow and have a depth of 3.5cm–6cm. The birds start arriving in the month of July and begin to occupy the earlier vacated nests, if available, or make new nests. Around third week of July, most of the trees in the nesting areas are occupied and the storks those arrive late had no option other than to choose a preoccupied nesting trees for nesting, which often resulted in intraspecific fighting. Collection of nesting material continues from July till November. The nesting materials include twigs, leaves and grasses. The number of chicks in the AOS nests varies from 1–3 (Figure 2). We observed chick in some AOS nests around mid August, and the young storks feeding on snail (weaning) was sighted in first week of October (Figure 2). During this four–year study period, we observed increasing trend in the number of occupied nests (Figure 3). AOS nests were recorded in 212.75±16.32 trees on which 2117.75±415.89 nests and 8477.5±1658.76 number of storks was observed during study period (Table 1). The highest number of trees with nests are of P. hyaeneanum (33.01%) followed by S. noxvomica (12.81%), A. indica (8.58%) and G. maulata (8.11%) (Figure 4). The highest number of nests are recorded in Pterospermium hyaeneanum (38%), followed by S. noxvomica (14%), F. bengalensis (11%) and A. indica (7%) (Figure 5). Nesting of AOS occurred 73m to 89m away from the roads. Most of the stork leave the nesting site by December except few those stay as resident birds.

Figure 2 Nesting of openbill stork at Nandankanan Wildlife Sanctuary, India. 1) Colonial nests of AOS, 2) roosting openbill storks, 3) nest with two surviving hatchlings, 4) nest with 3 surviving hatchlings. 5) AOS fledgling fallen on ground, 6) fledgling feeding on feeding on snail.

Figure 3 Number of nest and number of AOS during study period (2015-18).

Figure 4 Trees used for nesting by AOS and its species composition.

Figure 5 Percentage of nests in each tree species used for nesting of AOS.

Sl. No.

Name of the tree used for nesting

No. of trees

No. of nests

No. of Open bill storks

2015

2016

2017

2018

2015

2016

2017

2018

2015

2016

2017

2018

1

Pterospermium hyaeneanum

55

54

69

103

525

510

817

1403

2124

2040

3268

5612

2

Strychnos noxvomica

18

25

31

35

258

305

282

396

1028

1220

1128

1584

3

Azadirachta indica

25

17

11

20

195

102

116

223

362

408

464

892

4

Ehretia laevis

8

8

7

10

43

45

39

108

319

180

156

432

5

Streblus asper

15

18

6

10

79

89

36

73

219

356

144

292

6

Putranjiba rosburghii

0

0

5

9

0

0

31

191

0

0

144

764

7

Diospyros melanoxylon

0

0

0

9

0

0

0

108

0

0

0

432

8

Pongamia pinnata

0

0

3

8

0

0

58

101

0

0

232

404

9

Terminalia arjuna

0

0

3

2

0

0

85

36

0

0

340

144

10

Ficus bengalensis

15

17

7

1

357

412

69

68

782

1648

276

272

11

Adina cordifolia

7

8

7

1

50

55

51

17

205

220

204

68

12

Aegle marmelus

7

6

2

1

37

30

15

10

170

120

60

40

13

Melia azedarach

0

0

0

1

0

0

0

7

0

0

0

28

14

Glyricidia maculate

25

29

15

0

80

92

59

0

315

368

236

0

15

Stereospermum colais

0

0

11

0

158

0

0

0

632

0

16

Alangium lamarkii

8

9

4

0

54

69

51

0

1430

276

204

0

17

Mimusops elengi

0

0

5

0

0

0

35

0

0

0

140

0

18

Cassia siamia

15

17

5

0

75

78

20

0

297

312

80

0

19

Syzyjium cumini

15

12

0

0

90

80

0

0

145

320

0

0

20

Diospyros ovalifolia

9

8

0

0

42

51

0

0

170

204

0

0

Total

222

228

191

210

1885

1918

1927

2741

7566

7672

7708

10964

Table 1 Year wise nesting details of openbill storks at Nandankanan Wildlife Sanctuary, Odisha, India

Discussion

The wetlands of NWS provide good food resources with minimal disturbances for the storks. Availability of water body in vicinity is instrumental in determining the vegetation pattern which in turn warrants adequate nest–site availability with sustainable food and nest–construction material for birds.14,15 We also believe the availability of resources and conducive environment at NWS may be the reason for nesting of AOS every year. Abundance of food resources in and around the heronry and the minimal disturbance due to the remoteness of the area are speculated to be the principal factors for this large congregation of breeding birds.8,16 Nesting in mixed colonies during monsoon was reported.1 But in the present case mono–specific nesting was observed. At Bhitarkanika National Park, Odisha, nesting of AOS was reports exclusively on E. agallocha trees and most of these trees are located in the centre of the heronry.16 Though AOS preferred P. hyaeneanum for nesting at the study site, it does not exclusively nest on this species. A total of 20 different nesting tree species recorded in the present study. They also reported that AOS showed affinity to nest in the top canopy and their mean nest height was 14 ft (4.26m).16 We also observed similar affinity of AOS to nest on top canopy but the nesting height varies from 4.57m–10.67m (15–35 feet).

Nests are semi–circular to circular in shape and measured 30.21±0.12cm in radius and with a depth of 6.9±0.02cm approximately.17 The present study found similar shape of nests as described by Kanaujia et al.17 with 22–35cm radius and 3–5cm of depth. The nesting materials include twigs, leaves and grasses. Collection of nesting material continues from July till November. Both the sexes help to brood and feed the chicks.3 Movement of the chicks in the nest reported at the age of 4–5 weeks onwards, whereas young birds observed flying to short distances from the nest at about 60 days.6 Asian Openbill mainly feeds on the molluscs of Pila sp. by inserting the tip of the mandible and dislodging the molluscan body from the shell apart from the regular notion that the gap in the bill is used like a nutcracker to crack the molluscan shell.3 The gap in the bill is absent in the juveniles. The juveniles feed on regurgitated feed on the nest.3,17 We observed chick in the nest around mid August. While in the nest the chicks were fed with regurgitated feed from parent storks. During first week of October the young storks feeding on snail was sighted as a sign of weaning. The area adjacent to visitor path was left up to 73m to 89m without nesting by the storks though similar vegetation available in those areas. Besides they are know be least affected anthropogenic activity with a sound breeding record in the human disturbed areas.1,18

The dependence of storks on the particular nesting site makes the protection and scientific management crucial for their conservation. The present study described some major aspects of nest and nesting habits of AOS. The identification of tree species used as nesting material, behaviour of the storks during nest building, incubation and local migration to be studied further.

Acknowledgements

The authors are thankful to Prof. Sudarsan Maharana for his valuable suggestions in improvement of the manuscript.

Conflict of interest

Author declares no conflicts of interest.

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