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
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