Journal of Threatened Taxa | www.threatenedtaxa.org | 26 October 2023 | 15(10): 23996–24008

 

ISSN 0974-7907 (Online) | ISSN 0974-7893 (Print) 

https://doi.org/10.11609/jott.8283.15.10.23996-24008

#8283 | Received 25 November 2022 | Final received 22 September 2023 | Finally accepted 03 October 2023

 

 

Assessing avian diversity and conservation status in Dighal Wetlands, Haryana, India

 

Parul 1 & Parmesh Kumar 2

 

1,2 Department of Zoology, Institute of Integrated and Honors Studies, Kurukshetra University, Kurukshetra, Haryana 136119, India.

1 parulmaham@gmail.com (corresponding author), 2 parmesh@kuk.ac.in

 

 

 

Editor: H. Byju, Coimbatore, Tamil Nadu, India.        Date of publication: 26 October 2023 (online & print)

 

Citation: Parul & P. Kumar (2023). Assessing avian diversity and conservation status in Dighal Wetlands, Haryana, India. Journal of Threatened Taxa 15(10): 23996–24008. https://doi.org/10.11609/jott.8283.15.10.23996-24008

  

Copyright: © Parul & Kumar 2023. Creative Commons Attribution 4.0 International License.  JoTT allows unrestricted use, reproduction, and distribution of this article in any medium by providing adequate credit to the author(s) and the source of publication.

 

Funding: The research is funded by UGC in the form of SRF to one of the authors (Parul).

 

Competing interests: The authors declare no competing interests.

 

Author details: Dr. Parmesh Kumar is professor of Zoology, Department of Zoology, Institute of Integrated & Honors Studies, Kurukshetra University. He has published dozens of papers in the journals of national and international repute, and few book chapters on biodiversity specifically on avifauna of Haryana. His field of research includes wildlife ecology and animal behaviour. Parul is a research scholar and pursuing her Ph.D. from Department of Zoology, Kurukshetra University, Kurukshetra.

 

Author contributions: P. Kumar conceived and designed the study as well as wrote the final draft of the manuscript. Parul performed the field surveys, analysed the data and prepared rough draft of the manuscript. Both authors read and approved the final manuscript.

 

Acknowledgements: We are highly thankful to the Department of Zoology, Kurukshetra University, Kurukshetra for providing the requisite facilities. One of the authors, Parul is thankful to the University Grants Commission (UGC), New Delhi, India for providing financial support in the form of SRF to conduct this research work.

 

 

Abstract: Birds are considered sensitive indicators of ecosystem health and functionality in freshwater wetlands. Assessment of bird assemblages in wetland habitats is, therefore, emphasised from a sustainable management perspective. Bird surveys were conducted from October 2020 to September 2022. These surveys aimed to assess the community composition and status of avifauna in Dighal wetlands, an important bird area in the Jhajjar District of Haryana, India. Data collection employed   point counts and opportunistic encounter methods. A total of 154 bird species belonging to 108 genera, 47 families, and 18 orders were recorded. Of these, 75 species were residents, 60 were winter migrants, and 10 were summer migrants. The greatest species richness was observed for the order Passeriformes (54), followed by Charadriiformes (22), Anseriformes (17), and the rest of the 15 orders. Anatidae was the most dominant family with 17 species, constituting 11% of the bird community in the study area. Data on local abundance revealed that 10 species were common, 23 were fairly common, 83 were uncommon, and 38 were rare in the study area. Among the recorded avifauna, one species is classified as Endangered, three as Vulnerable, and eight as Near Threatened in the IUCN Red List of Threatened Species; 17 species are listed in the Appendices of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES); and 11 are included in Schedule I of the Indian Wildlife (Protection) Act, 1972. These wetlands also support 40 species of birds, which have a declining population trend globally. The occurrence of migrants and species of global conservation priority underscores the importance of these wetlands as a conservation site and wintering ground for avifauna due to the extensive food resources and rich biodiversity they support. The present study provides baseline information for future research on monitoring bird assemblages and proper management of the Dighal wetlands of Haryana. 

 

Keywords: Assemblages, biodiversity, birds, community composition, ecosystem, indicator, migrants, point counts, species richness, threatened species.

 

 

INTRODUCTION

 

Wetlands are dynamic ecosystems that link aquatic and terrestrial habitats (Zedler & Kercher 2005; Bassi et al. 2014; Panda et al. 2021; Rajpar et al. 2022; Yashmita-Ulman & Singh 2022). They have specific ecological characteristics, functions, and values. Approximately 5–8% of the Earth’s surface is occupied by wetlands (Anand et al. 2023). In addition to providing various ecosystem services, wetlands are reservoirs of incredible biodiversity, including invertebrates, fish, amphibians, reptiles, birds, mammals, and plants. Therefore, wetlands are often viewed as treasuries of biodiversity within a region or landscape (Bhat et al. 2009; Singh & Brraich 2022; Anand et al. 2023; Byju et al. 2023).  

Birds occupy several trophic levels in the nutrient cycle of wetland ecosystems (Kumar & Sharma 2018; Chakraborty et al. 2021; Rai & Vanita 2021; Rajpar et al. 2022; Yashmita-Ulman & Singh 2022). Wetlands are important for both resident and migratory birds. They are used by birds for various purposes such as foraging, breeding, roosting, and nesting habitats, and sometimes also as stopover sites (Ganbold et al. 2018; Kumar & Sharma 2018; Panda et al. 2021; Yashmita-Ulman & Singh 2022; Anand et al. 2023; Muralikrishnan et al. 2023). Birds are extremely sensitive to changes in their habitats such as human disturbance, poisoning, pollution, eutrophication, and siltation; therefore, they can be used as an excellent ecological indicator for assessing the quality, productivity, and stability of wetlands (Mistry et al. 2008; Amat & Green 2010).

In India, 4.6% of the geographical area is under wetlands (Bassi et al. 2014; Anand et al. 2023). Of the 1,353 bird species reported from various habitats within the geographical limits of India (Praveen & Jayapal 2023), 310 are recognised to be dependent on wetlands (Kumar et al. 2005). However, wetlands in India, as elsewhere, are facing anthropogenic pressures like conversion of wetlands into agricultural lands or for commercial fishing purposes, industrial pollution, fertilisers run-off from surrounding agricultural fields, hunting, unsustainable harvest of wetland resources, invasion of alien species, eutrophication, and draining of water for agricultural purposes (Ganbold et al. 2018; Kumar & Sharma 2018; Mandal et al. 2021; Panda et al. 2021; Rashiba et al. 2022; Yashmita-Ulman & Singh 2022). This threatens the existing avifaunal diversity of wetlands. Information on species composition and seasonal assemblages of birds in a particular wetland habitat is very helpful in understanding the habitat condition and designing suitable conservation and management strategies for sustainable biodiversity conservation (Kumar et al. 2016; Ganbold et al. 2018; Mandal et al. 2021; Muralikrishnan et al. 2023).

Dighal wetlands have been identified as an Important Bird and Biodiversity Area (IBA) of India with the IBA code of IN-HR-06 by the ENVIS Centre on Wildlife and Protected Areas (Rahmani et al. 2016). Spread over an area of about 131.5 ha, Dighal wetlands in the Jhajjar District of Haryana are a complex of many small and large ponds along with vast areas of wet fields left for several years because of high water table and water logging conditions in the Dighal Village. These wetlands serve as important wintering sites for large congregations of migratory birds. To understand the anthropogenic impacts on wetland birds and their habitat in the future, it is essential to have information on the species composition, seasonality, and conservation status of bird assemblages. Such information will help in the long-term monitoring of the wetlands and preparing conservation and management strategies for the avifauna as well as their habitat. In this context, the present study was designed to document the community composition and status of avifauna in the Dighal wetlands of Haryana, India.

 

 

MATERIAL AND METHODS

 

Study area

The present study was conducted in the Dighal wetlands, located in the southeastern region of Haryana state, India, with coordinates at 28.222°N and 76.187°E. These wetlands, positioned within Beri Tehsil of Jhajjar District, encompass an area of approximately 131.5 ha , comprising a complex of ponds, both small and large, as well as extensive wet fields that have remained unused for several years due to consistent high water tables and recurrent waterlogging in the village of Dighal. As a critical part of the Central Asian Flyway, the Dighal wetlands serve as crucial wintering grounds for numerous migratory bird species. This research involved selecting eight specific wetland sites for bird surveys, with their key characteristics detailed in Table 1. The study area experiences a subtropical climate featuring three distinct seasons: a rainy period from July to September, a cool dry season from October to February, and a hot dry season from March to June. Temperatures range from a scorching 45°C in summer to a chilly 6°C in winter, with an average annual rainfall of 444 mm recorded in the district.

 

Data collection

Avian surveys were conducted using the point count method, following a bi-weekly schedule from October 2020 to September 2022. Four to six counting points, spaced at least 250 m apart, were strategically positioned along the perimeter of the wetlands, totaling 48 surveys at each location over the study period. A five-minute settling period preceded ten minutes of active bird observation, employing Nikon 10x50 field binoculars during peak activity hours (0600–1000 h or 1600–1800 h). Additional opportunistic observations were carried out by scanning the wetlands’ peripheries and banks to compile a comprehensive avifauna checklist. Bird identification followed Grimmett et al. (2011), with Praveen & Jayapal (2023) for taxonomic references. Abundance status relies on sighting frequency, which can be categorised as common (CO), fairly common (FC), uncommon (UC), or rare (RA) based on Mackinnon & Phillipps (1993). The residential status (resident, summer migrant, or winter migrant) was determined with the presence-absence method (Kumar & Sharma 2018). Conservation status aligned with IWPA (1972) and CITES (2012), while the Red List of the IUCN (2022) guided assessment for conservation status and global population trend.

Relative diversity (RDi) of bird families was computed as

             Number of Bird Species in a Family

RDi  = –––––––––––––––––––––––––––––––  x 100

               Total Number of Bird Species

 

following the Torre-Cuadros et al. (2007) formula.

 

RESULTS

 

A total of 154 species of birds belonging to 108 genera, 47 families, and 18 orders were recorded from the study area (Table 2). Passeriformes was the most dominant order with 54 species, followed by Charadriiformes (22), Anseriformes (17), and the rest 15 orders (Figure 2). Analysis of the relative diversity index revealed that Anatidae was the most diverse family (17 species, RDi = 11.03), followed by Scolopacidae (13 species, RDi = 8.44), Muscicapidae (10 species, RDi = 7.46), and Accipitridae (9 species, RDi = 5.84). Whereas 16 families, namely, Phoenicopteridae, Podicipedidae, Anhingidae, Jacanidae, Burhinidae, Strigidae, Bucerotidae, Upupidae, Megalaimidae, Picidae, Coraciidae, Dicruridae, Nectariniidae, Phylloscopidae, Zosteropidae, and Rhipiduridae were least represented (one species each, RDi = 0.64) (Table 3).

Of the total bird species recorded, 75 species (49%) were resident, 69 species (45%) were winter migrants, and only 10 species (6%) were summer visitors (Figure 3). Based on the IUCN Red List of Threatened Species, one species, Egyptian Vulture Neophron percnopterus is ‘Endangered’, and three species—Common Pochard Aythya farina, Sarus Crane Antigone antigone, and River Tern Sterna aurantia—are ‘Vulnerable’; eight species—Ferruginous Duck Aythya nyroca, Painted Stork Mycteria leucocephala, Woolly-necked Stork Ciconia episcopus, Black-headed Ibis Threskiornis melanocephalus, Oriental Darter Anhinga melanogaster, Black-tailed Godwit Limosa limosa, Eurasian Curlew Numenius arquata, and Alexandrine Parakeet Psittacula eupatria—are ‘Near Threatened’; and the rest 142 species are Least Concern (Table 2). About the global population trend, the wetlands supported 62 globally stable species, 40 globally decreasing species, 29 globally increasing species, and 23 species whose global trend was unknown (Table 2). Data on local abundance revealed that 10 species were common, 23 species were fairly common, 83 species were uncommon, and 38 species were rare in the study area. It is pertinent here to mention that among the 38 species recorded rarely in the study area, 12 species—Ferruginous Duck Aythya nyroca, Mallard Anas platyrhynchos, Greater Flamingo Phoenicopterus roseus, Demoiselle Crane Grus virgo, Common Snipe Gallinago gallinago, Common Kingfisher Alcedo atthis, Isabelline Shrike Lanius isabellinus, White-eared Bulbul Pycnonotus leucotis, Red-breasted Flycatcher Ficedula parva, Osprey Pandion haliaetus, Oriental Honey Buzzard Pernis ptilorhynchus, and White-browed Fantail Rhipidura aureola—were spotted only once or twice during the study period. Comparison of the local abundance status of recorded avian species with their global population trend revealed that three species—Indian Spot-billed Duck Anas poecilorhyncha, Rock Pigeon Columba livia, and Little Grebe Tachybaptus ruficollis—had a globally declining population trend and were found to be common in the study area (Figure 4). In addition to this, one species recorded from these wetlands was listed in Appendix I, and 16 species were listed in Appendix II of CITES (Table 1). According to the IWPA (1972), out of 154 recorded species, 11 were under Schedule I, one was in Schedule V, and the rest (n = 142) were in Schedule IV (Table 1).

 

 

DISCUSSION

 

The study area boasts an impressive avian diversity, contributing to approximately 29% of the bird species recorded in Haryana (Kalsi et al. 2020) and 11% of India’s avifauna (Praveen & Jayapal 2023). The findings suggest that the avifaunal richness observed in the studied wetlands aligns with previous research conducted in various regions of Haryana (Table 4). Nevertheless, it is important to note that Alfred et al. (2001) documented 216 wetland bird species in the more expansive Sub-Himalayan Terai and Indo-Gangetic Plains of northern India. In the survey, Passeriformes were identified as the dominant order, with 54 species representing 18 families. These results corroborate earlier records highlighting Passeriformes as the primary avian taxa in India (Praveen & Jayapal 2023).

Among the documented bird families in the selected wetlands of Jhajjar District, Anatidae emerged as the most diverse. This observation aligns with prior studies demonstrating Anatidae as a prevalent bird family in various freshwater wetlands across India (Tak et al. 2010; Kumar & Sharma 2018; Rai et al. 2019; Kaur & Brraich 2021; Singh & Brraich 2022; Yashmita-Ulman & Singh 2022). The findings indicate that the majority of recorded species are residents, followed by winter and summer visitors, consistent with earlier reports on freshwater wetlands in Haryana (Kumar & Gupta 2013; Kumar et al. 2016; Rai et al. 2019). It is worth noting that 20 bird species recorded as migrants in the study area are considered residents of Haryana (Kalsi et al. 2020), as outlined in Table 2. Given Haryana’s location within the Central Asian Flyway, it serves as a crucial wintering ground for migratory birds travelling from northern Asia and parts of Europe (Kumar et al. 2016; Kumar & Sharma 2018; Rai & Vanita 2021).

The suitability of the Dighal wetlands, surrounded by irrigated agricultural fields featuring wheat and paddy crops, as well as tree species like Safeda (Eucalyptus spp.), Kikar (Acacia spp.), and Ber (Ziziphus spp.) along the wetland edges, provides ample resources for migratory birds during the winter months. This resource availability contributes to the rich avian diversity, particularly during the winter season.

The survey identified 12 bird species of global conservation significance, including one Endangered species, three Vulnerable species, and eight Near Threatened species. Furthermore, 17 species listed in the CITES appendices inhabit these wetlands. All the recorded bird species are also protected under various Schedules of the Indian Wildlife (Protection) Act, 1972. Notably, the study identified three species with declining global populations as common in the study area, indicating the continued availability of suitable resources for these species in the wetlands.

The presence of a substantial number of winter migrants and species of global conservation concern underscores the importance of these wetlands for avian conservation in Haryana.

However, wetland habitats across India face significant threats, including habitat loss, fragmentation, and degradation; water quality deterioration due to contamination; recreational pressures; and developmental activities (Kumar & Sharma 2018; Chakraborty et al. 2021; Kaur & Brraich 2021; Mandal et al. 2021; Yashmita-Ulman & Singh 2022; Anand et al. 2023; Muralikrishnan et al. 2023). The Dighal wetlands are no exception, as they support a diverse community of winter migrants and species of global conservation concern, all of which are vulnerable to various anthropogenic pressures. These threats include extensive fishing activities, electrocution, construction near ponds, domestic waste dumping, water drainage during the winter, and plastic pollution in ponds.

The study serves as a valuable baseline for future research on bird population monitoring and the effective management of the Dighal wetlands in the Jhajjar District of Haryana.

 

 

CONCLUSION

 

The documentation of 12 bird species of global conservation importance and 40 species of birds with a declining population trend globally emphasises the importance of studied wetlands from a  global bird conservation perspective. These wetlands, along with surrounding agricultural fields and plantations, provide a congenial habitat for both resident and migratory avian species. Therefore, these wetlands should be given conservation and research priorities and regularly assessed for their existing bird diversity. This study provides valuable information on the ecological health and status of these wetlands and will be useful for increasing awareness regarding their conservation value.

 

Table 1. General features of the selected Dighal wetland sites in Jhajjar District of Haryana, India.

Wetland site

Co-ordinates

General features

S1

28.780°N, 76.620°E

 

This wetland habitat is comprised of waterlogged agricultural fields spread on both sides of the Jhajjar-Rohtak toll plaza expressway. The roadside plantation was dominated by Eucalyptus trees.

S2

28.762°N, 76.636°E

A water-logged barren land on one side of one of the water houses of Dighal Village. It is comprised of small shrubs and bushy plantations all over the area.

S3

28.772°N, 76.635°E

This site is a complex of four adjoining ponds fragmented by road. It is surrounded by a gaushala, a graveyard, and a water house.

S4

28.772°N, 76.630°E

This pond is located on the back side of the sports stadium building and comprises comparatively less plantation.

S5

28.769°N, 76.627°E

 

This site is comprised of four ponds fragmented by road in the Dighal Village. An old historical monument is present on the bank of the pond and surrounded by human habitations.

S6

28.764°N, 76.626°E

This site is a single large pond located in front of the central co-operative bank of the Dighal Village and has a community health centre nearby.

S7

28.759°N, 76.629°E

This pond is present in the locality of residential areas and an old well is present on one corner of the pond.

S8

28.761°N, 76.634°E

This is a fragmented large pond in front of a water tank area, a natural small pond, and waterlogged agricultural land nearby.

 

Table 2. List of avian species recorded from Dighal wetlands of Jhajjar District, Haryana, India together with their respective taxonomic position, residential status, local abundance status, conservation status, and global population trend.

 

Common name/ Order

Scientific name

Family

Residential status

Local status

Conservation status

Global population trend

IUCN Red List

IWPA

CITES

Order ANSERIFORMES

1

Lesser-whistling Duck

Dendrocygna javanica

Anatidae (17)

S

UC

LC

IV

-

2

Bar-headed Goose

Anser indicus

 

W

FC

LC

IV

-

3

Greylag Goose

Anser anser

W

UC

LC

IV

-

4

Ruddy Shelduck

Tadorna ferruginea

W

UC

LC

IV

-

?

5

Red-crested Pochard

Netta rufina

W

RA

LC

IV

-

?

6

Common Pochard

Aythya farina

W

UC

VU

IV

-

7

Ferruginous Duck

Aythya nyroca

W

RA

NT

IV

-

8

Tufted Duck

Aythya fuligula

W

UC

LC

IV

-

9

Garganey

Spatula querquedula

W

UC

LC

IV

-

10

Northern Shoveler

Spatula clypeata

W

FC

LC

IV

-

11

Gadwall

Mareca strepera

W

UC

LC

IV

-

12

Eurasian Wigeon

Mareca penelope

W

UC

LC

IV

-

13

Indian Spot-billed Duck

Anas poecilorhyncha

R

CO

LC

IV

-

14

Northern Pintail

Anas acuta

W

UC

LC

IV

-

15

Common Teal

Anas crecca

W

UC

LC

IV

-

?

16

Knob-billed Duck

Sarkidiornis melanotos

W*

UC

LC

IV

II

17

Mallard

Anas platyrhynchos

W

RA

LC

IV

-

Order: GALLIFORMES

18

Indian Peafowl

Pavo cristatus

Phasianidae (2)

R

UC

LC

I

-

19

Grey Francolin

Francolinus pondicerianus

 

R

UC

LC

IV

-

Order: COLUMBIFORMES

20

Rock Pigeon

Columba livia

Columbidae (5)

R

CO

LC

IV

-

21

Eurasian Collared Dove

Streptopelia decaocto

 

R

FC

LC

IV

-

22

Spotted Dove

Streptopelia chinensis

R

UC

LC

IV

-

23

Laughing Dove

Streptopelia senegalensis

R

FC

LC

IV

-

24

Yellow-footed Green Pigeon

Treron phoenicopterus

R

RA

LC

IV

-

Order: CUCULIFORMES

25

Greater Coucal

Centropus sinensis

Cuculidae (4)

R

FC

LC

IV

-

26

Asian Koel

Eudynamys scolopaceus

 

S

UC

LC

IV

-

27

Grey-bellied Cuckoo

Cacomantis passerinus

S

RA

LC

IV

-

28

Pied Cuckoo

Clamator jacobinus

S

RA

LC

IV

-

Order: PHOENICOPTERIFORMES

29

Greater Flamingo

Phoenicopterus roseus

Phoenicopteridae (1)

W*

RA

LC

IV

-

Order: PODICIPEDIFORMES

30

Little Grebe

Tachybaptus ruficollis

Podicipedidae (1)

R

CO

LC

IV

-

Order: GRUIFORMES

31

White-breasted Waterhen

Amaurornis phoenicurus

Rallidae (4)

R

UC

LC

IV

-

?

32

Grey-headed Swamphen

Porphyrio poliocephalus

 

R

FC

LC

IV

-

?

33

Common Moorhen

Gallinula chloropus

 

R

CO

LC

IV

-

34

Eurasian Coot

Fulica atra

W

FC

LC

IV

-

35

Sarus Crane

Antigone antigone

Gruidae (2)

R

UC

VU

IV

II

36

Demoiselle Crane

Grus virgo

 

W

RA

LC

IV

II

Order: CICONIIFORMES

37

Painted Stork

Mycteria leucocephala

Ciconiidae (3)

R

FC

NT

IV

I

38

Asian Openbill

Anastomus oscitans

 

R

UC

LC

IV

-

?

39

Woolly-necked Stork

Ciconia episcopus

R

FC

NT

IV

-

 

 

40

Black-crowned Night Heron

Nycticorax nycticorax

Ardeidae (8)

R

UC

LC

IV

-

41

Indian Pond Heron

Ardeola grayii

 

R

CO

LC

IV

-

?

42

Cattle Egret

Bubulcus ibis

R

CO

LC

IV

-

43

Grey Heron

Ardea cinerea

R

UC

LC

IV

-

?

44

Purple Heron

Ardea purpurea

R

UC

LC

IV

-

45

Great Egret

Ardea alba

R

UC

LC

IV

-

?

46

Intermediate Egret

Ardea intermedia

R

UC

LC

IV

-

47

Little Egret

Egretta garzetta

R

UC

LC

IV

-

48

Black-headed Ibis

Threskiornis melanocephalus

Threskiornithidae (4)

R

FC

NT

IV

-

49

Red-naped Ibis

Pseudibis papillosa

 

R

UC

LC

IV

-

50

Glossy Ibis

Plegadis falcinellus

W*

UC

LC

IV

-

51

Eurasian Spoonbill

Platalea leucorodia

W*

UC

LC

I

II

?

 

 

52

Little Cormorant

Microcarbo niger

Phalacrocoracidae (3)

R

FC

LC

IV

-

?

53

Great Cormorant

Phalacrocorax carbo

 

W

UC

LC

IV

-

54

Indian Cormorant

Phalacrocorax fuscicollis

R

FC

LC

IV

-

?

55

Oriental Darter

Anhinga melanogaster

Anhingidae (1)

W*

UC

NT

IV

-

 

 

56

Pied Avocet

Recurvirostra avosetta

Recurvirostridae (2)

W

UC

LC

IV

-

?

57

Black-winged Stilt

Himantopus himantopus

 

R

CO

LC

IV

-

58

Little-ringed Plover

Charadrius dubius

Charadriidae (4)

W*

RA

LC

IV

-

59

Red-wattled Lapwing

Vanellus indicus

 

R

CO

LC

IV

-

?

60

Yellow-wattled Lapwing

Vanellus malabaricus

W*

RA

LC

IV

-

61

White-tailed Lapwing

Vanellus leucurus

W

UC

LC

IV

-

?

62

Black-tailed Godwit

Limosa limosa

Scolopacidae (13)

W

UC

NT

IV

-

63

Marsh Sandpiper

Tringa stagnatilis

 

W

UC

LC

IV

-

64

Green Sandpiper

Tringa ochropus

W

UC

LC

IV

-

65

Spotted Redshank

Tringa erythropus

W

RA

LC

IV

-

66

Little Stint

Calidris minuta

W

UC

LC

IV

-

67

Temminck's Stint

Calidris temminckii

W

UC

LC

IV

-

?

68

Common Snipe

Gallinago gallinago

W

RA

LC

IV

-

69

Common Sandpiper

Actitis hypoleucos

W

UC

LC

IV

-

70

Common Redshank

Tringa totanus

 

W

UC

LC

IV

-

?

71

Common Greenshank

Tringa nebularia

W

RA

LC

IV

-

72

Ruff

Calidris pugnax

W

UC

LC

IV

-

73

Wood Sandpiper

Tringa glareola

W

UC

LC

IV

-

74

Eurasian Curlew

Numenius arquata

W

RA

NT

IV

-

75

Black-headed Gull

Chroicocephalus ridibundus

Laridae (2)

W

RA

LC

IV

-

?

76

River Tern

Sterna aurantia

 

W*

UC

VU

IV

-

77

Pheasant-tailed Jacana

Hydrophasianus chirurgus

Jacanidae (1)

S

RA

LC

IV

-

78

Indian Thick-knee

Burhinus indicus

Burhinidae (1)

W*

RA

LC

IV

-

 

 

79

Osprey

Pandion haliaetus

Accipitridae (9)

W

RA

LC

I

II

80

Oriental Honey Buzzard

Pernis ptilorhynchus

 

W*

RA

LC

I

II

81

Black-winged Kite

Elanus caeruleus

R

UC

LC

I

II

82

Egyptian Vulture

Neophron percnopterus

W*

UC

EN

I

II

83

Shikra

Accipiter badius

R

UC

LC

I

II

84

Brahminy Kite

Haliastur indus

W

RA

LC

I

II

85

Black Kite

Milvus migrans

R

FC

LC

I

II

86

Eurasian Sparrowhawk

Accipiter nisus

W

RA

LC

I

II

87

Short-toed Snake Eagle

Circaetus gallicus

W

RA

LC

I

II

 

 

88

Spotted Owlet

Athene brama

Strigidae (1)

R

UC

LC

IV

II

 

 

89

Indian Grey Hornbill

Ocyceros birostris

Bucerotidae (1)

R

UC

LC

IV

-

90

Common Hoopoe

Upupa epops

Upupidae (1)

R

UC

LC

IV

-

 

 

91

Brown-headed Barbet

Psilopogon zeylanicus

Megalaimidae (1)

R

RA

LC

IV

-

92

Black-rumped Flameback

Dinopium benghalense

Picidae (1)

R

RA

LC

IV

-

 

 

93

Pied Kingfisher

Ceryle rudis

Alcedinidae(3)

R

UC

LC

IV

-

?

94

White-throated Kingfisher

Halcyon smyrnensis

 

R

FC

LC

IV

-

?

95

Common Kingfisher

Alcedo atthis

W*

RA

LC

IV

-

?

96

Indian Roller

Coracias benghalensis

Coraciidae (1)

R

UC

LC

IV

-

97

Green Bee-eater

Merops orientalis

Meropidae (2)

S

UC

LC

IV

-

98

Blue-cheeked Bee-eater

Merops persicus

 

S

RA

LC

IV

-

 

 

99

Alexandrine Parakeet

Psittacula eupatria

Psittaculidae (2)

R

UC

NT

IV

II

100

Rose-ringed Parakeet

Psittacula krameri

 

R

FC

LC

IV

-

 

 

101

Black Drongo

Dicrurus macrocercus

Dicruridae (1)

R

CO

LC

IV

-

?

102

Isabelline Shrike

Lanius isabellinus

Laniidae (2)

W

RA

LC

IV

-

103

Long-tailed Shrike

Lanius schach

 

R

UC

LC

IV

-

?

104

Rufous Treepie

Dendrocitta vagabunda

Corvidae (3)

R

UC

LC

IV

-

105

House Crow

Corvus splendens

 

R

CO

LC

V

-

106

Large-billed Crow

Corvus macrorhynchos

R

UC

LC

IV

-

107

Purple Sunbird

Cinnyris asiaticus

Nectariniidae (1)

R

UC

LC

IV

-

108

Indian Silverbill

Euodice malabarica

Estrildidae (3)

R

UC

LC

IV

-

109

Scaly-breasted Munia

Lonchura punctulata

 

R

UC

LC

IV

-

110

Red Munia

Amandava amandava

W*

RA

LC

IV

-

111

House Sparrow

Passer domesticus

Passeridae (2)

R

FC

LC

IV

-

112

Sind Sparrow

Passer pyrrhonotus

 

W*

RA

LC

IV

-

113

Crested Lark

Galerida cristata

Alaudidae (2)

R

UC

LC

IV

-

114

Bengal Bushlark

Mirafra assamica

 

S

RA

LC

IV

-

115

Plain Prinia

Prinia inornata

Cisticolidae (5)

R

UC

LC

IV

-

116

Graceful Prinia

Prinia gracilis

 

S*

RA

LC

IV

-

117

Zitting Cisticola

Cisticola juncidis

R

UC

LC

IV

-

118

Ashy Prinia

Prinia socialis

R

FC

LC

IV

-

119

Common Tailorbird

Orthotomus sutorius

R

UC

LC

IV

-

120

White-eared Bulbul

Pycnonotus leucotis

Pycnonotidae (2)

W*

RA

LC

IV

-

121

Red-vented Bulbul

Pycnonotus cafer

 

R

FC

LC

IV

-

122

Common Chiffchaff

Phylloscopus collybita

Phylloscopidae (1)

W

UC

LC

IV

-

123

Brahminy Starling

Sturnia pagodarum

Sturnidae (3)

S*

RA

LC

IV

-

?

124

Common Starling

Sturnus vulgaris

 

W

RA

LC

IV

-

125

Asian Pied Starling

Gracupica contra

R

FC

LC

IV

-

126

Red-breasted Flycatcher

Ficedula parva

Muscicapidae (10)

W

RA

LC

IV

-

127

Black Redstart

Phoenicurus ochruros

 

W

RA

LC

IV

-

128

Common Myna

Acridotheres tristis

R

FC

LC

IV

-

129

Bank Myna

Acridotheres ginginianus

R

FC

LC

IV

-

130

Indian Robin

Copsychus fulicatus

R

UC

LC

IV

-

131

Oriental Magpie Robin

Copsychus saularis

R

UC

LC

IV

-

132

Bluethroat

Luscinia svecica

W

RA

LC

IV

-

133

Brown Rock Chat

Oenanthe fusca

R

UC

LC

IV

-

134

Siberian Stonechat

Saxicola maurus

W

UC

LC

IV

-

135

Pied Bushchat

Saxicola caprata

R

UC

LC

IV

-

136

Rosy Pipit

Anthus roseatus

Motacillidae (8)

W

UC

LC

IV

-

137

Tawny Pipit

Anthus campestris

 

W

UC

LC

IV

-

138

Long-billed Pipit

Anthus similis

W

UC

LC

IV

-

139

Paddyfield Pipit

Anthus rufulus

R

UC

LC

IV

-

140

Western Yellow Wagtail

Motacilla flava

W

UC

LC

IV

-

141

Citrine Wagtail

Motacilla citreola

W

UC

LC

IV

-

142

White-browed Wagtail

Motacilla maderaspatensis

W*

FC

LC

IV

-

143

White Wagtail

Motacilla alba

W

UC

LC

IV

-

144

Streak-throated Swallow

Petrochelidon fluvicola

Hirundinidae (4)

R

UC

LC

IV

-

145

Wire-tailed Swallow

Hirundo smithii

 

R

FC

LC

IV

-

146

Barn Swallow

Hirundo rustica

W

UC

LC

IV

-

147

Grey-throated Martin

Riparia chinensis

W*

UC

LC

IV

-

148

Indian White-eye

Zosterops palpebrosus

Zosteropidae (1)

R

UC

LC

IV

-

149

Jungle Babbler

Argya striata

Leiothrichidae (2)

R

UC

LC

IV

-

150

Large grey Babbler

Argya malcolmi

 

R

UC

LC

IV

-

151

Streaked Weaver

Ploceus manyar

Ploceidae (3)

R

UC

LC

IV

-

152

Baya Weaver

Ploceus philippinus

 

R

UC

LC

IV

-

153

Black-breasted Weaver

Ploceus benghalensis

R

UC

LC

IV

-

154

White-browed Fantail

Rhipidura aureola

Rhipiduridae (1)

W*

RA

LC

IV

-

Residential Status: R—Resident | S—Summer Migrant | W—Winter Migrant.

Local Abundance Status: CO—Common | FC—Fairly Common | UC—Uncommon | RA—Rare.

IUCN Red List: LC—Least Concern | NT—Near Threatened | VU—Vulnerable | EN—Endangered.

IWPA (Indian Wildlife Protection Act, 1972): I— Schedule I | IV—Schedule IV,

Global Population Trend: ↑—Increasing | ↓—Decreasing | →—Stable | ?—Unknown.

*—Species that are resident in Haryana but recorded only in winter or summer in the study area.

 

Table 3. Relative diversity index (RDi) of various bird families in Dighal wetlands of Jhajjar District of Haryana.

Bird families

Number of species

RDi value

Anatidae

17

11.03

Scolopacidae

13

8.44

Muscicapidae

10

7.46

Accipitridae

9

5.84

Ardeidae, Motacillidae

8

5.19

Columbidae, Cisticolidae

5

3.24

Cuculidae, Rallidae, Threskiornithidae, Charadriidae, Hirundinidae

4

2.59

Ciconiidae, Phalacrocoracidae, Alcedinidae, Corvidae, Estrildidae, Sturnidae, Ploceidae

3

1.94

Phasianidae, Gruidae, Recurvirostridae, Laridae, Meropidae, Psittaculidae, Laniidae, Passeridae, Alaudidae, Pycnonotidae, Leiothrichidae

2

1.29

Phoenicopteridae, Podicipedidae, Anhingidae, Jacanidae, Burhinidae, Strigidae, Bucerotidae, Upupidae, Megalaimidae, Picidae, Coraciidae, Dicruridae, Nectariniidae, Phylloscopidae, Zosteropidae, Rhipiduridae

1

0.64

 

Table 4. A comparison of avifauna recorded from different study areas of Haryana, India.

 

Study area

Recorded avifauna

Reference

Species

Family

Order

1

Khaparwas Bird Sanctuary, district Jhajjar

164

44

16

Gupta et al. 2012

2

Sultanpur National Park, district Gurugram

161

47

16

Kaushik & Gupta 2016

3

Kalesar National Park, district Yamunanagar

126

51

14

Rai et al. 2017

4

Basai Wetland, district Gurugram

171

51

17

Rai et al. 2019

5

Bhindawas Bird Sanctuary, district Jhajjar

119

43

17

Singh & Malik 2019

6

Sultanpur National Park, district Gurugram

111

42

17

Singh et al. 2021

7

Ottu Reservoir, district Sirsa

114

47

18

Rai & Vanita 2021

 

 

For figures & images - - click here for full PDF

 

 

REFERENCES

 

Alfred, J.R.B. (2001). Waterbirds of Northern India. Zoological Survey of India, Kolkata, xxvi+468 pp.

Amat, J.A. & A.J. Green (2010). Waterbirds as Bioindicators of Environmental Conditions, pp. 45–52. In: Hurford, C., M. Schneider & I. Cowx (eds.). Conservation Monitoring in Freshwater Habitats. Springer, Dordrecht, 187 pp. https://doi.org/10.1007/978-1-4020-9278-7_5   

Anand, J., H. Byju, A. Nefa, S. Abhijith, O.R. Reshi & K.M. Aarif (2023). Conservation significance of Changaram wetlands - a key wintering site for migratory shorebirds and other waterbirds in the western coast of Kerala, India. Journal of Threatened Taxa 15(1): 22410–22418. https://doi.org/10.11609/jott.8089.15.1.22410-22418 

Bassi, N., M.D. Kumar, A. Sharma & P.P. Saradhi (2014). Status of wetlands in India: a review of extent, ecosystem benefits, threats and management strategies. Journal of Hydrology: Regional Studies 2: 1–19. https://doi.org/10.1016/j.ejrh.2014.07.001

Bhat, I.P., S.S. Cristopher & B.B. Hosetti (2009). Avifaunal diversity of Anekere wetland, Karkala Udupi district, Karnataka, India. Journal of Environmental Biology 30(6): 1059–1062.

Bibby, C.J., N.D. Burgess, D.A. Hill & S.H. Mustoe (2000). Bird Census Techniques. Academic Press, London, 302 pp.

Byju, H., N. Raveendran, S. Ravichandran & R. Kishore (2023). An annotated checklist of the avifauna of Karangadu mangrove forest, Ramanathapuram, Tamil Nadu, with notes on the site’s importance for waterbird conservation. Journal of Threatened Taxa 15(3): 22813–22822. https://doi.org/10.11609/jott.8356.15.3.22813-22822

Chakraborty, A., H. Barman, G.K. Saha & G. Aditya (2021). Wintering waterbird assemblage in an emerging wetland of West Bengal, India: characterization for conservation management. Ornis Hungarica 29(1): 1–19. https://doi.org/10.2478/orhu-2021-0001

CITES (2012). Convention on International Trade in Endangered Species of Wild Fauna & Flora. CITES, Geneva, Switzerland. Downloaded on 20 October 2022. https://www.cites.org

Ganbold, O., G.C. Bing, J.H. Lee, M. Munkhbayar, I.H. Paik, A. Jargalsaikhan, E. Purevee, Z. Purevdorj & W.K. Paek (2018). An avifaunal survey of middle Mongolian wetlands: Important Bird Areas and threatened species. Journal of Asia-Pacific Biodiversity 11(3): 340–345. https://doi.org/10.1016/j.japb.2018.06.007

Grimmett, R., C. Inskipp & T. Inskipp (2011). Birds of the Indian Subcontinent. Oxford University Press & Christopher Helm, London, 528 pp.

Gupta, R.C., M. Parashar & T.K. Kaushik (2012). Documentation of avian diversity of Khaparwas Bird Sanctuary in Jhajjar district in Haryana, India. International Journal of Life Sciences 6(1): 20–30.

IUCN (2022). The IUCN Red List of Threatened Species. Version 2021–1. Downloaded on 20 October 2022; https://www.iucnredlist.org.

IWPA (1972).The Indian Wildlife (Protection) Act, 1972 (as amended up to 2022). Ministry of Environment, Forest and Climate Change, Government of India, Delhi. https://www.envfor.nic.in/legis/wildlife/wildlife1. Downloaded on 20 October 2022.

Kalsi, R.S., S.C. Sharma & J.R. Choudhary (2020)Birds of Haryana- A Field Guide. Unique Publications, Panipat, Haryana, 602 pp.

Kaur, R. & O.S. Brraich (2021). Abundance and diversity of the threatened birds in Nangal Wetland, Punjab, India. Journal of Threatened Taxa 13(12): 19733–19742. https://doi.org/10.11609/jott.4062.13.12.19733-19742

Kaushik, T.K. & R.C. Gupta (2016). Status and diversity of avifauna in Sultanpur National Park in Gurgaon district-Haryana, India. Indian Forester 142(10): 19733–19742.

Kumar, A., J.P. Sati, P.C. Tak & J.R.B. Alfred (2005). Handbook on Indian Wetland Birds and their Conservation. Zoological Survey of India, Kolkata, 468 pp.

Kumar, P. & A. Sharma (2018). Wetland birds assemblages in man-made sacred ponds of Kurukshetra, India. Proceedings of the Zoological Society 72(1): 61–73. https://doi.org/10.1007/s12595-018-0259-x   

Kumar, P. & S.K. Gupta (2013). Status of wetland birds of Chhilchhila Wildlife Sanctuary, Haryana, India. Journal of Threatened Taxa 5(5): 3969–3976. https://doi.org/10.11609/JoTT.o3158.3969-76

Kumar, P., D. Rai & S.K. Gupta (2016). Wetland bird assemblage in rural ponds of Kurukshetra, India. Waterbirds 39(1): 86–98. https://doi.org/10.1675/063.039.0111

MacKinnon, J. & K. Phillipps (1993). A Field Guide to Birds of Sumatra, Java and Bali, the Greater Sunda Islands. Oxford University Press, Oxford, 692 pp.

Mandal, M.H., A. Roy & G. Siddique (2021). A geographical assessment of Chariganga and Arpara Beel (wetlands) of Nadia, West Bengal as a habitat of wetland birds. Journal of Threatened Taxa 13(13): 19964–19975. https://doi.org/10.11609/jott.6257.13.13.19964-19975

Mistry, J., A. Berardi & M. Simpson (2008). Birds as indicators of wetland status and change in the North Rupununi, Guyana. Biodiversity and Conservation 17: 2383–2409. https://doi.org/10.1007/s10531-008-9388-2

Muralikrishnan, S., E. Shanmugam, N.A. Nagendran & D. Pandiaraja (2023). Diversity and abundance of aquatic birds in Koonthankulam village pond, Tamil Nadu, India. Journal of Threatened Taxa 15(6): 23297–23306. https://doi.org/10.11609/jott.6612.15.6.23297-23306

Panda, B.P., A.K. Das, S.K. Jena, B. Mahapatra, A.K. Dash, A. Pradhan & S.P. Parida (2021). Habitat heterogeneity and seasonal variations influencing avian community structure in wetlands. Journal of Asia-Pacific Biodiversity 14(1): 23–32. https://doi.org/10.1016/j.japb.2020.10.001

Praveen, J. & R. Jayapal (2023). Taxonomic updates to the checklists of birds of India and the South Asian region. Indian Birds 18(5): 131–134. https://www.indianbirds.in/india/

Rahmani, A.R., M.Z. Islam & R.M. Kasambe (2016). Important Bird and Biodiversity Areas in India: Priority Sites for Conservation (Revised and updated). Bombay Natural History Society, Indian Bird Conservation Network, Royal Society for the Protection of Birds and BirdLife International (U.K.), 1992+xii pp.

Rai, D. & Vanita (2021). Community composition and status of avifaunal diversity in and around Ottu reservoir of Sirsa, Haryana, India. Journal of Applied and Natural Sciences 13(2): 593–606. https://doi.org/10.31018/jans.v13i2.2666

Rai, D., G. Chopra, R. Gulia & P. Vats (2017). Avian diversity of Basai wetlands, Haryana (India): an IBA site. Journal of Experimental Zoology India 20(1): 109–117.

Rai, D., P. Vats, & R. Gulia (2017). Avifaunal status of Kalesar National Park, Haryana (India). Journal of Experimental Zoology India 20(2): 827–833.

Rai, D., R. Gulia, G. Chopra & P. Kumar (2019). Avifaunal community composition and current status in Basai wetlands: an important bird area in Haryana, India. Indian Forester 145(10): 971–985. https://doi.org/10.36808/if%2F2019%2Fv145i10%2F149234

Rajpar, M.N., S. Ahmad, M. Zakaria, A. Ahmad, X. Guo, G. Nabi & K. Wanghe (2022). Artificial wetlands as alternative habitat for a wide range of waterbird species. Ecological Indicators 138(12): 108855. https://doi.org/10.1016/j.ecolind.2022.108855

Rashiba, A.P., K. Jishnu, H. Byju, C.T. Shifa, J. Anand, K. Vichithra, Y. Xu, A. Nefla, S.B. Muzaffar, K.M. Aarif & K.A. Rubeena (2022). The paradox of shorebird diversity and abundance in the West Coast and East Coast of India: a comparative analysis. Diversity 14(10): 885. https://doi.org/10.3390/d14100885    

Singh, J. & O. S. Brraich (2022). Seasonal composition of avian communities in different habitats of Harike wetland, a Ramsar site in Punjab, India. Journal of Threatened Taxa 14(2): 20550–20565. https://doi.org/10.11609/jott.7581.14.2.20550-20565

Singh, J. & V. Malik. (2019). Diversity and status of avifauna in Bhindawas Bird Sanctuary, Haryana, India. Annals of Biology 35(2): 280–284.

Singh, J., S. Hooda, A. Phogat & V. Malik (2021). Avian diversity and habitat use of Sultanpur National Park, Haryana, India. Asian Journal of Conservation Biology 10(1): 124–133. https://doi.org/10.53562/ajcb.RKPR3560

Tak, P.C., J.P. Sati & A.N. Rizvi (2010). Status of waterbirds at Hathnikund Barrage wetland, Yamunanagar district, Haryana, India. Journal of Threatened Taxa 2(4): 841–844. https://doi.org/10.11609/JoTT.o2200.841-4   

Torre-Cuadros, L., M. De Los Ángeles, S. Herrando-Pérez & K.R. Young (2007). Diversity and structural patterns for tropical montane and premontane forests of central Peru, with an assessment of the use of higher-taxon surrogacy. Biodiversity and Conservation 16: 2965–2988. https://doi.org/10.1007/s10531-007-9155-9

Yashmita-Ulman & M. Singh (2022). Avifaunal diversity in unprotected wetlands of Ayodhya District, Uttar Pradesh, India. Journal of Threatened Taxa 14(8): 21561–21578. https://doi.org/10.11609/jott.7067.14.8.21561-21578

Zedler, J.B. & S. Kercher (2005). Wetland resources: status, trends, ecosystem services, and restorability. Annual Review of Environment and Resources 30: 39–74; https://doi.org/10.1146/annurev.energy.30.050504.144248