Journal of Threatened Taxa | www.threatenedtaxa.org | 26
December 2019 | 11(15): 14989–14997
An
assessment of bird communities across Ujjani and its
five satellite wetlands in Solapur District of Maharashtra, India
Shraddha Prabhakar Karikar 1, Subhash Vitthal
Mali 2, Kulkarni Prasad 3 & Aphale
Priti 4
1,4 Department
of Environmental Science, Fergusson College (Autonomous), affiliated to
Savitribai Phule Pune University, Pune, Maharashtra 411004, India.
2 Department of
Environmental Science, Savitribai Phule Pune University, Pune, Maharashtra
411007, India.
3 School of
Ecology, Society and Sustainable Development, Faculty of Social Innovation,
Partnership and Co-creation; MIT-World Peace University, Pune 411038, India.
1 shraddhakarikar@gmail.com
(corresponding author), 2 subhash.environment@gmail.com, 3 prasad.kulkarni@mitwpu.edu.in,
4 aphale.priti@gmail.com
doi: https://doi.org/10.11609/jott.4741.11.15.14989-14997
|
ZooBank: urn:lsid:zoobank.org:pub:167D431E-0D06-40A7-AC2E-3023FA6F175D
Editor: M. Zafar-ul Islam, National
Wildlife Research Center, Saudi Arabia. Date
of publication: 26 December 2019 (online & print)
Manuscript details: #4741 | Received 03 December
2018 | Final received 20 November 2019 | Finally accepted 29 November 2019
Citation: Karikar, S.P., S.V. Mali, K. Prasad
& A. Priti (2019). An assessment of bird communities across Ujjani and its five satellite wetlands in Solapur District
of Maharashtra, India. Journal of Threatened Taxa 11(15): 14989–14997. https://doi.org/10.11609/jott.4741.11.15.14989-14997
Copyright: © Karikar et al. 2019. Creative Commons Attribution
4.0 International License. JoTT allows unrestricted use, reproduction, and
distribution of this article in any medium by adequate credit to the author(s)
and the source of publication.
Funding: This study is
partially funded by Board of College and
University Development (BCUD), Savitribai Phule Pune University Pune.
Competing interests: The authors declare no competing
interests.
Author details: Dr. Shraddha Prabhakar Karikar worked on habitat conservation
of wetlands, aquatic bird communities and their preference analysis by applying
various statistical models. Dr. Subhash Vitthal
Mali worked on conservation biology of Malabar Giant Squirrel, species
recovery of endangered medicinal plants, joint forest management, environmental
impact assessments and environment management of industrial projects. Dr.
Prasad Anil Kulkarni is interested in change detection mapping of
Mangrove Ecosystem of Raigad Coast, Maharashtra. Ecosystem monitoring and its
conservation related research. Life member of Indian Society of Remote Sensing.
Member IUCN-CEC-1176(2017-20), Fellow of United Nations University for
International Course on Mangroves Biodiversity and Ecology. Ms. Priti Vinayak Aphale is
interested in habitat ecology studies and conservation related research. Worked
on sacred groves of Maval Tahsil, Pune Maharashtra,
India since 2012 with special reference to community participation in
conservation.
Author contribution: SPK-—contributed in research idea development and its implementation on
field, sample collection and analysis. SVM—contributed in designing of
experiments and provided critical remarks on manuscript. PAK—provided inputs for deciding study area
and sampling sites. Also contributed in technical aspects for wetland
mapping. PVA—contributed in wetland
ecosystem monitoring, field data collection and identification of bird species.
Acknowledgements:
We are sincerely gratified to our
family members for their constant support and encouragement. We are
appreciative to local communities of Kumbhargaon and Bhadalwadi for their support during the field surveys. We are thankful to Mr. Rahul Kale, Advt. Mahesh
Kahnerkar, Mr. Mahesh Ekale
and students of Fergusson College for their support during the fieldwork. We
are grateful to BCUD, SPPU, Pune for funding this research. We thank Dr. Ashwini Rane for her
off-field support.
Abstract: Ujjani
wetland is a potential Ramsar site in Maharashtra,
India with several satellite wetlands associated with it. The present study contributes to
single large or several small habitat conservation theories
by assessing wetland bird communities.
Aquatic bird communities were assessed using area search and point count
methods at Kumbhargaon (Ujjani),
Bhadalwadi, Madanwadi, Palasdev, Pimple and Ravangaon
wetlands between October 2011 and September2012. These are representative satellite wetlands
around Ujjani.
One-hundred-and-ten species of wetland birds across 12 orders and 29
families were recorded. Out of these, 66
were resident and 44 were found to be migrants. These birds represent 23% mudflat feeder, 16%
upland feeder, 14% marsh feeder, 12% bird of prey, 11% surface feeder and fish
eaters, while divers and wet meadow feeders were represented with 8.5% and 5%
of the species, respectively. Among the
birds recorded, Woolly-necked Stork Ciconia episcopus, Common
Pochard Aythya farina, and Greater
Spotted Eagle Clanga clanga
belong to the Vulnerable category; while Eurasian Curlew Numenius
arquata, Oriental Darter Anhinga melanogaster,
Black-tailed Godwit Limosa limosa, Black-headed Ibis Threskiornis
melanocephalus, Lesser Flamingo Phoeniconaias minor, Painted Stork Mycteria leucocephala,
River Tern Sterna aurantia, and Great
Thick-knee Esacus recurvirostris
represent Near Threatened category on the IUCN Red List. The presence of these bird species underlines
the importance and conservation priorities of a major as well as smaller
satellite wetlands. Anthropogenic
activities such as cattle grazing, fishing, sand and soil mining, land
encroachment, urban development and tourism were observed as some of the
threats to this wetland ecosystem as well as bird communities.
Keywords:
Aquatic birds, Ramsar site, SLOSS, wetland bird
communities.
Introduction
Wetlands are distinct zones intermediate between
terrestrial and aquatic ecosystem where the water table is usually at or near
the surface of the land and is covered by shallow water (Semeniuk & Semeniuk 1995). Wetlands are the most productive ecosystems
in the world (Mitsch et al. 2009). Natural and man-made reservoirs form small
heterogenous water patches in their vicinity.
Such small wetlands associated with large streams are called satellite
wetlands (Bedford 1996; Novitski et al. 1996; Patten
et al. 2008).
Wetlands maintain the health of the environment and
support a rich biodiversity. They
complete habitat requirements of various water birds. Birds are excellent indicators of wetland
health (Kumar & Gupta 2013). Habitat
protection is important to conserve bird communities associated with it.
Large wetlands normally receive all the importance
while smaller and isolated wetlands receive least attention and are often
neglected from conservation priorities.
Many studies have focused on major and larger wetlands while very few
scientific investigations have been undertaken on comparatively small, isolated
and not so well-known wetlands. In the
absence of such studies, smaller and isolated wetlands are neglected from
appearing in conservation priorities even if they are located in the vicinity
of a major wetland.
On a theoretical conservation perspective,
single large or several small (SLOSS) habitats debate is
well known; many ecologists argue for one large habitat while an equal number
of scientists advocate for many small habitats (Ma et al. 2010). It was argued that species
richness increases with habitat area and hence larger block of
habitat would support more species than any of the smaller blocks. Further, Simberloff
& Abele (1976) contested that if the smaller protected area had unshared
species, then it is possible that two smaller reserves could have more species
than a single large reserve.
Before we take any stand on such perspectives, it is
primarily required to initiate studies that compares a large wetland and many
smaller ones. Such studies can help in
deciding conservation priorities in fragmented habitats. In this context, the present study explores
the status of bird communities harboured at one large wetland and several small
satellite wetlands associated with it. Ujjani wetland and its satellite wetlands were assessed for
this work.
The Ujjani Dam is an
earthen-cum-masonry gravity dam located on river Bhima. The Bhima River is a tributary of river
Krishna that originates in the ranges of the Western Ghats. This dam is amongst the largest dams in
Maharashtra, situated near Ujjani Village of Solapur
District. The dam was primarily built
for irrigating water -scarce fields. It is located at 18.2990N &
74.7630E, 465m. This region
is a plain expanse with negligible slope and the reservoir is spread across 348
km2 (Mahabal et al. 2011). It has more of shallow areas at the fringe
parts of the reservoir, that provide a distinctive habitat for the
avifauna. The Ujjani
wetland is a potential Ramsar site in Maharashtra (Samant 2002; Islam & Rahmani
2008).
Material and Methods
Study area
The Ujjani wetland has a
huge expanse and to overcome practical difficulty in sampling, Kumbhargaon (18.2660N & 74.8050E,
494m), a representative location of Ujjani wetland
was selected for sampling as it covers very shallow to very deep-water
areas. As Ujjani
wetland is dam backwater, similar type of five man-made satellite wetlands,
viz., Bhadalwadi (18.2340N & 74.7810E,
511m), Madanwadi (18.2850N & 74.7070E,
515m), Ravangaon (18.3300N & 74.6130E,
556m), Pimple (18.2470N & 74.7290E, 516m), and Palasdev (18.2110N & 74.8650E,
507m) associated with Ujjani wetland was selected for
the present study. In order to know the
exact location of these wetlands, satellite imagery was superimposed on the
toposheet. A map of these sites was
prepared to indicate relative locations of these wetlands with respect to Ujjani with the help of QGIS 2.18 (Image 1).
Bird survey
The study was conducted between October 2011 and
September 2012. Counts were conducted
near the wetland where all or most of the surface area and edge were visible
(Bibby et al. 2000). The survey duration
includes the time required to thoroughly scan a wetland. Sampling was conducted using area search and
point count method. Point counts were
taken for areas where visibility is obstructed like marshy area and upland
vegetation. No two-point counts were
taken within a distance of 200m. Care was taken to ensure that birds were
recorded only once (Bibby et al. 2000, Weller 1999). Area search methods were used for areas with
clear visibility like open water. The
accessible edges of wetlands were walked around to detect any unseen birds. The
birds were observed during the peak hours of their activity from sunrise to
10.00h and 16.00–18.00 h using Olympus (8 x 40 mm, 10 x 50 mm) binoculars. Identification of birds was done using field
guides (Ali & Ripley 1995; Grimmett et al. 2013),
and only those species with confirmed identity were recorded and reported.
Data classification and analysis
Recording and listing of these birds were done using
standard common and scientific names (Praveen
et al. 2016). Residential status
of the birds as resident and migrants had been assigned with reference to the
study area on the basis of presence or absence method. The status of the recorded bird species was
established on the basis of frequency of sightings (Kumar & Gupta 2009) as
Abundant (A) recorded 9–10 times out of 10 visits, Common (C) recorded 7–8
times out of 10 visits, Frequent (F) recorded 5-6 times out of 10 visits,
Occasional (O) recorded 3–5 times out of 10 visits, Rare(R) recorded 0–2 times
out of 10 visits (Therivel & Morris 1995).
Birds were delineated in eight feeding categories as
bird of prey, fish eaters, divers, mudflat feeder, marsh feeder, wet meadow,
surface feeder ducks, and upland feeders (Gole 1993).
To compare wetlands, a cluster analysis was performed
on the presence of bird communities. Cluster
analysis was performed using Jaccard’s similarity measure and a paired group
method by PAST 3 software (Field & McFarlane 1968; Day & Edelsbrunner 1984; Washington 1984; Hartzell et al. 2007). The conservation status of the observed
species was listed using the IUCN Red List, 2016 ver3.1 (IUCN 2016).
Results and Discussion
One-hundred-and-ten species of wetland bird genera
belonging to 12 orders and 29 families were recorded from Kumbhargaon
(Ujjani) and its satellite wetlands between October
2011–September 2012.
The checklist of birds observed, identified and
recorded in the region along with their family and resident status is provided
in Table 1. It was observed that Anatidae (16 species) followed by Scolopacidae
(14 species) were the most represented families of the study area (Figure 1); whereas,
Anhingidae, Dicruridae, Falconidae, Gruidae, Meropidae, Pandionidae, Podicipedidae, Recurvirostridae,
and Rostratulidae were represented by just a single
genus and least represented.
Among the recorded species 66 species were resident
and 44 migratory. Relative abundance
studies revealed that six species were abundant, 21 species were common, 46
species were frequent, 25 occasional and 12 were rare. Woolly-necked Stork Ciconia episcopus, Common
Pochard Aythya farina and Greater
Spotted Eagle Clanga clanga
were found to belong to the Vulnerable category of the IUCN and their number is
found to be decreasing globally; while Eurasian Curlew Numenius
arquata, Oriental Darter Anhinga melanogaster,
Black-tailed Godwit Limosa limosa, Black-headed Ibis Threskiornis
melanocephalus, Lesser Flamingo Phoeniconaias minor, Painted Stork Mycteria leucocephala,
River Tern Sterna aurantia, and Great
Thick-knee Esacus recurvirostris
represent the Near Threatened (NT) category of IUCN Red List.
Feeding class-wise distribution of observed species
indicated that mudflat feeders were most common with 23% species, followed by
upland feeders with 16%, marsh feeders with 14%, bird of prey with 12 %,
surface feeders and fish eaters each with 11%, while divers and wet meadow
feeders were represented with 8.5% and 5% of the species, respectively (Figure
2).
Relative abundance analysis indicates Common Coot Fulica atra as most
abundant at Kumbhargoan (Ujjani)
and Palasdev while Oriental Darter Anhinga
melanogaster and Eurasian Curlew Numenius
arquata were least abundant. The Painted Stork Mycteria
leucocephala and Rosy Starling Pastor roseus
were found to be most abundant at Bhadalwadi wetland
and Eurasian Curlew Numenius arquata, Pheasant-tailed Jacana Hydrophasianus
chirurgus were least abundant. At Madanwadi
wetland Common Sandpiper Actitis hypoleucos, Little Ringed Plover Charadrius
dubius showed highest relative abundance and
Eurasian Thick-knee Burhinus oedicnemus, Great Cormorant Phalacrocorax
carbo recorded the lowest. The
Common Coot Fulica atra
and Brahminy Starling Sturnia pagodarum were found to be most abundant at
Pimple and Ravangaon wetland respectively while Great
Egret Ardea alba and Common Moorhen Gallinula chloropus
were found to be least abundant.
When Shannon-Weiner diversity and evenness across
satellite wetlands were calculated, it was found to be 3.5, 0.37 at Kumbhargoan (Ujjani) followed by
3.5, 0.38 at Palasdev; 3.1, 0.42 at Madanwadi, 2.6, 0.45 at Pimple, 2.5, 0.22 at Bhadalwadi, and 2.2, 0.33 Ravangaon
wetland at p<0.05.
Jaccard’s similarity index was calculated from the
record of occurrence of the bird species across these wetlands. It was observed
that, Kumbhargaon (Ujjani)
and Palasdev were most similar wetlands with index
value of 0.88, while Kumbhargaon (Ujjani)
and Ravangaon were most dissimilar in their species
composition with index value of 0.36. Kumbhargaon (Ujjani) and Bhadalwadi was more
similar with index value of 0.59 followed by Kumbhargaon
(Ujjani) and Madanwadi with
reported value of 0.49. Kumbhargaon (Ujjani) and Pimple to were among least similar wetlands
with value of 0.4. It reveals that, out
of five associated wetlands of Ujjani reservoir; Palasdev, Bhadalwadi and Madanwadi wetlands show high resemblance and similarity for
the inhabitation of wetland bird communities.
Bird communities harboured by Ujjani and Ravangaon wetland were fairly distinct. Detailed cluster
analysis paired (UPGMA) of Jaccard’s similarity Index of each wetland was shown
in Figure 3.
Present study provides checklist of wetland bird
communities at Ujjani as well as its five satellite
wetlands. Of the 110 bird species
recorded at Kumbhargoan (Ujjani)
wetland, 94 were recorded at Palasdev, while 59, 54,
31, and 29 species were reported at Bhadalwadi, Madanwadi, Pimple, and Ravangaon
wetlands, respectively. Vital base line
information on the presence and abundance of bird communities based on
sightings were collected. Ujjani and other wetlands
have shallow water expanse resulting in rich abundance and diversity of bird
communities.
The wetland bird communities are in general heterogeneous in their
feeding habitat (Kumar & Gupta
2013). The diversity of the wetland
birds observed at other satellite wetlands may indicate a presence of a wide
spectrum of feeding niches. In the
present study agriculture fields surrounding the Kumbhargaon
(Ujjani) wetland
and satellite wetlands with scattered plants, viz., Acacia species, Zizyphus species, and Tamarindus
species, probably provide diverse
roosting and foraging habitation grounds to the bird communities.
A comparison of bird communities of main wetlands with
its satellite wetlands revealed that, some of the satellite wetlands support an
almost equal number of bird species to that of the main wetland. Also, all these satellite wetlands together
share, more than 95% of the total bird species composition of Ujjani wetland. Presence of the threatened bird species highlights
the significance of the wetland as an important conservation site (Islam & Rahmani 2004, 2008) and wintering ground for wetland birds. From conservation priorities both large as
well as small wetlands are important. Reduction
in existing anthropogenic activities like cattle grazing, fishing, sand and
soil mining, land encroachment, urban development, and tourism would improve
conservation status of bird communities.
Detailed studies on physical characterization of wetlands and habitat
preference by bird communities are necessary to understand the role of
satellite wetlands in the conservation of avifauna.
Table 1. Status of birds recorded at Ujjani and its satellite wetlands, Maharashtra.
|
Family
& Species |
Wetland |
Month |
Resident
status |
Abundance |
Red
List Status |
|
Accipitridae |
|
|
|
|
|
1 |
Black-winged Kite Elanus caeruleus |
Uj, Bh, Ma, Pa, Ra |
Jan–Dec |
R |
F |
LC |
2 |
Black Kite Milvus migrans |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
F |
LC |
3 |
Brahminy Kite Haliastur indus |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
C |
LC |
4 |
Greater Spotted Eagle Clanga clanga |
Uj |
Feb |
M |
O |
VU |
5 |
Crested Serpent Eagle Spilornis cheela |
Uj, Bh, Pa, Ra |
Jan–Dec |
R |
F |
LC |
6 |
Western Marsh Harrier Circus aeruginosus |
Uj, Bh, Pa |
Dec–Feb |
M |
F |
LC |
7 |
Montagu's Harrier Circus pygargus |
Uj,
Pa |
Dec–Feb |
M |
R |
LC |
8 |
Bonelli's
Eagle Aquila fasciata |
Uj,
Ra |
Nov–Feb |
R |
O |
LC |
9 |
Tawny Eagle Aquila rapax |
Uj,
Ma, Ra |
Jan–Dec |
R |
O |
LC |
10 |
Short-toed Snake Eagle Circaetus gallicus |
Uj, Bh, Pa, Ra |
Jan–Dec |
R |
O |
LC |
11 |
Shikra Accipiter
badius |
Uj,
Pa |
Sep–Dec |
R |
O |
LC |
|
Alaudidae |
|
|
|
|
|
12 |
Indian Bushlark
Mirafra erythroptera |
Uj,
Ma, Pa, Ra |
Jan–Dec |
R |
C |
LC |
13 |
Rufous-tailed Lark Ammomanes phoenicura |
Uj,
Ma |
Jan–Dec |
R |
F |
LC |
|
Alcedinidae |
|
|
|
|
|
14 |
Common Kingfisher Alcedo atthis |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
C |
LC |
15 |
Pied Kingfisher Ceryle rudis |
Uj, Bh, Pa |
Jan–Dec |
R |
F |
LC |
16 |
White-throated Kingfisher Halcyon
smyrnensis |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
F |
LC |
|
Anatidae |
|
|
|
|
|
17 |
Indian Spot-billed Duck Anas poecilorhyncha |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
C |
LC |
18 |
Comb Duck Sarkidiornis
melanotos |
Uj,
Pa |
Oct–Mar |
R |
R |
LC |
19 |
Lesser Whistling Duck Dendrocygna javanica |
Uj, Bh, Pa |
Jan–Dec |
R |
C |
LC |
20 |
Tufted Duck Aythya
fuligula |
Uj, Bh, Pa |
Nov–Feb |
M |
O |
LC |
21 |
Eurasian Wigeon Mareca penelope |
Uj, Bh, Pa |
Nov–Mar |
M |
O |
LC |
22 |
Gadwall Mareca
strepera |
Uj, Bh, Pa |
Nov–Feb |
M |
F |
LC |
23 |
Garganey Spatula querquedula |
Uj, Bh, Ma, Pa, Pi, Ra |
Oct–Mar |
R |
F |
LC |
24 |
Bar-headed Goose Anser indicus |
Uj,
Pa |
Nov–Mar |
M |
F |
LC |
25 |
Cotton Teal Nettapus
coromandelianus |
Uj, Bh, Ma, Pa |
Oct–Jan |
R |
O |
LC |
26 |
Northern Pintail Anas acuta |
Uj, Bh, Pa |
Nov–Feb |
M |
F |
LC |
27 |
Northern Shoveler
Spatula clypeata |
Uj, Bh, Pa |
Nov–Mar |
M |
O |
LC |
28 |
Common Pochard Aythya ferina |
Uj, Bh, Pa |
Jan–Feb |
M |
R |
VU |
29 |
Red-crested Pochard Netta rufina |
Uj,
Pa |
Jan–Feb |
M |
R |
LC |
30 |
Ruddy Shelduck Tadorna ferruginea |
Uj, Bh, Ma, Pa |
Nov–Mar |
M |
F |
LC |
31 |
Common Teal Anas crecca |
Uj, Bh, Pa, Pi |
Nov–Feb |
R |
F |
LC |
32 |
Common Shelduck Tadorna tadorna |
Uj, Bh, Ma, Pa |
Dec–Jan |
M |
R |
LC |
|
Anhingidae |
|
|
|
|
|
33 |
Oriental Darter Anhinga
melanogaster |
Uj, Bh, Ma, Pa |
Oct–Feb |
R |
R |
NT |
|
Ardeidae |
|
|
|
|
|
34 |
Cattle Egret Bubulcus
ibis |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
C |
LC |
35 |
Great Egret Ardea
alba |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
C |
LC |
36 |
Intermediate Egret Ardea intermedia |
Uj, Bh, Ma, Pa |
Jan–Dec |
R |
F |
LC |
37 |
Little Egret Egretta
garzetta |
Uj, Bh, Ma, Pa, Pi |
Jan–Dec |
R |
C |
LC |
38 |
Black-crowned Night Heron Nycticorax nycticorax |
Uj, Bh, Ma, Pa |
Jan–Dec |
R |
O |
LC |
39 |
Grey Heron Ardea
cinerea |
Uj, Bh, Ma, Pa, Pi, Ra |
Oct–May |
R |
C |
LC |
40 |
Indian Pond Heron Ardeola grayii |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
C |
LC |
41 |
Striated Heron Butorides striata |
Uj, Bh, Ma, Pa, Pi |
Jan–Dec |
R |
F |
LC |
42 |
Purple Heron Ardea
purpurea |
Uj, Bh, Ma, Pa |
Jan–Dec |
R |
F |
LC |
|
Burhinidae |
|
|
|
|
|
43 |
Eurasian Thick-knee Burhinus oedicnemus |
Uj,
Ma, Pa, Pi |
Jan–Dec |
R |
O |
LC |
44 |
Great Thick-knee Esacus recurvirostris |
Uj, Bh, Pa |
Jan–Dec |
R |
R |
NT |
|
Charadriidae |
|
|
|
|
|
45 |
Red-wattled
Lapwing Vanellus indicus |
Uj, Bh, Ma, Pa, Pi,Ra |
Jan–Dec |
R |
F |
LC |
46 |
Yellow-wattled
Lapwing Vanellus malabaricus |
Uj,
Ma, Pa |
Jan–Dec |
R |
O |
LC |
47 |
Kentish Plover Charadrius alexandrinus |
Uj,
Ma |
Nov–Feb |
R |
O |
LC |
48 |
Little Ringed Plover Charadrius dubius |
Uj,
Ma, Pa, Pi |
Jan–Dec |
R |
A |
LC |
|
Ciconiidae |
|
|
|
|
|
49 |
Asian Openbill Anastomus oscitans |
Uj, Bh, Pa |
Jan–Dec |
R |
F |
LC |
50 |
Painted Stork Mycteria leucocephala |
Uj, Bh, Pa |
Jan–Dec |
R |
C |
NT |
51 |
European White Stork Ciconia ciconia |
Uj,
Pa |
Nov–Jan |
R |
F |
LC |
52 |
Woolly-necked Stork Ciconia episcopus |
Uj, Bh, Ma, Pa |
Oct–Dec |
R |
O |
VU |
|
Dicruridae |
|
|
|
|
|
53 |
Black Drongo
Dicrurus macrocercus |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
C |
LC |
|
Falconidae |
|
|
|
|
|
54 |
Common Kestrel Falco tinnunculus |
Uj,
Pa, Ra |
Nov–Feb |
M |
C |
LC |
|
Glareolidae |
|
|
|
|
|
55 |
Collared Pratincole Glareola pratincola |
Uj,
Ma |
Oct–May |
M |
F |
LC |
56 |
Oriental Pratincole Glareola maldivarum |
Uj,
Ma |
Oct–May |
M |
F |
LC |
57 |
Little Pratincole Glareola lactea |
Uj,
Ma, Pa |
Jan–Dec |
R |
A |
LC |
|
Gruidae |
|
|
|
|
|
58 |
Demoiselle Crane Grus virgo |
Uj |
Jan |
M |
O |
LC |
|
Hirundinidae |
|
|
|
|
|
59 |
Barn Swallow Hirundo
rustica |
Uj, Bh, Ma, Pa, Pi, Ra |
Oct–Jan |
M |
C |
LC |
60 |
Wire-tailed Swallow Hirundo smithii |
Uj, Bh, Ma, Pa, Pi, Ra |
Oct–Jan |
M |
F |
LC |
|
Jacanidae |
|
|
|
|
|
61 |
Bronze-winged Jacana Metopidius indicus |
Uj, Bh |
Jul |
R |
R |
LC |
62 |
Pheasant-tailed Jacana Hydrophasianus chirurgus |
Uj, Bh |
Aug |
R |
R |
LC |
|
Laniidae |
|
|
|
|
|
63 |
Bay-backed Shrike Lanius vittatus |
Uj, Bh, Ma, Pa, Pi |
Jan–Dec |
R |
C |
LC |
64 |
Long-tailed Shrike Lanius schach |
Uj,
Pa, Ra |
Jan–Dec |
R |
C |
LC |
|
Laridae |
|
|
|
|
|
65 |
Black-headed Gull Chroicocephalus ridibundus |
Uj,
Pa |
Nov–Feb |
M |
F |
LC |
66 |
Brown-headed Gull Chroicocephalus brunnicephalus |
Uj,
Pa |
Nov–Feb |
M |
F |
LC |
67 |
Pallas's Gull Ichthyaetus ichthyaetus |
Uj,
Pa |
Dec–Jan |
M |
O |
LC |
68 |
Caspian Tern Hydroprogne
caspia |
Uj,
Pa |
Dec–Mar |
M |
F |
LC |
69 |
Gull-billed Tern Gelochelidon nilotica |
Uj,
Pa |
Dec–Mar |
M |
F |
LC |
70 |
River Tern Sterna aurantia |
Uj,
Pa |
Dec–Mar |
M |
F |
NT |
71 |
Whiskered Tern Chlidonias hybrida |
Uj,
Pa |
Jan–Mar |
R |
F |
LC |
|
Meropidae |
|
|
|
|
|
72 |
Green Bee-eater, Merops
orientalis |
Uj, Bh, Pa, Pi, Ra |
Jan–Dec |
R |
C |
LC |
|
Motacillidae |
|
|
|
|
|
73 |
Citrine
Wagtail Motacilla citreola |
Uj,
Ma, |
Nov–Feb |
M |
F |
LC |
74 |
Grey Wagtail Motacilla
cinerea |
Uj,
Ma, Pa |
Nov–Feb |
M |
C |
LC |
75 |
White-browed Wagtail Motacilla maderaspatensis |
Uj,
Ma, Ra |
Jan–Dec |
R |
F |
LC |
76 |
Western Yellow Wagtail Motacilla flava |
Uj,
Pa |
Nov–Feb |
M |
C |
LC |
77 |
White Wagtail Motacilla alba |
Uj |
Jan–Feb |
M |
F |
LC |
|
Pandionidae |
|
|
|
|
|
78 |
Osprey Pandion haliaetus |
Uj,
Pa |
Dec–Feb |
M |
O |
LC |
|
Phalacrocoracidae |
|
|
|
|
|
79 |
Great Cormorant Phalacrocorax carbo |
Uj, Bh, Ma, Pa, |
Oct–Jan |
R |
F |
LC |
80 |
Indian Cormorant Phalacrocorax fuscicollis |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
A |
LC |
81 |
Little Cormorant Microcarbo niger |
Uj, Bh, Ma, Pa, Pi, Ra |
Jan–Dec |
R |
A |
LC |
82 |
Greater Flamingo Phoenicopterus roseus |
Uj,
Pa |
Jan–Feb |
M |
O |
LC |
83 |
Lesser Flamingo Phoeniconaias minor |
Uj,
Pa |
Feb–Mar |
M |
R |
NT |
|
Podicipedidae |
|
|
|
|
|
84 |
Little Grebe Tachybaptus
ruficollis |
Uj, Bh, Ma, Pa, Pi |
Jan–Dec |
R |
A |
LC |
|
Rallidae |
|
|
|
|
|
85 |
Common Coot Fulica
atra |
Uj, Bh, Pa, Pi |
Jan–Dec |
R |
A |
LC |
86 |
Common Moorhen Gallinula chloropus |
Uj, Bh, Ma, Pa, Pi |
Jul–Oct |
R |
F |
LC |
87 |
Purple Swamphen
Porphyrio porphyrio |
Uj, Bh, Ma, Pa, Pi |
Jan–Dec |
R |
F |
LC |
88 |
White-breasted Waterhen Amaurornis phoenicurus |
Uj, Bh, Ma, Pa, Pi |
Jul–Oct |
R |
F |
LC |
|
Recurvirostridae |
|
|
|
|
|
89 |
Black-winged Stilt Himantopus himantopus |
Uj,
Ma, Pa, Ra |
Jan–Dec |
R |
C |
LC |
|
Rostratulidae |
|
|
|
|
|
90 |
Greater Painted-snipe Rostratula benghalensis |
Uj,
Pa |
Jan–Dec |
R |
O |
LC |
|
Scolopacidae |
|
|
|
|
|
91 |
Eurasian Curlew Numenius arquata |
Uj, Bh |
Nov–Mar |
R |
R |
NT |
92 |
Black-tailed Godwit Limosa limosa |
Uj,
Pa |
Nov–Feb |
M |
F |
NT |
93 |
Common Greenshank Tringa nebularia |
Uj,
Ma, Pa |
Nov–Mar |
M |
F |
LC |
94 |
Common Redshank Tringa totanus |
Uj,
Ma, Pa |
Oct–Mar |
R |
F |
LC |
95 |
Spotted Redshank Tringa erythropus |
Uj,
Pa |
Oct–Par |
R |
O |
LC |
96 |
Ruff Calidris
pugnax |
Uj,
Pa |
Nov–Dec |
R |
R |
LC |
97 |
Common Sandpiper Actitis hypoleucos |
Uj,
Ma, Pa |
Nov–May |
M |
F |
LC |
98 |
Green Sandpiper Tringa ochropus |
Uj,
Pa |
Nov–May |
M |
F |
LC |
99 |
Marsh Sandpiper Tringa stagnatilis |
Uj,
Pa |
Nov–Jan |
M |
O |
LC |
100 |
Wood Sandpiper Tringa glareola |
Uj,
Pa |
Jan–Apr |
M |
O |
LC |
101 |
Common Snipe Gallinago
gallinago |
Uj, Bh, Ma, Pa |
Nov–Feb |
M |
F |
LC |
102 |
Pintail Snipe Gallinago stenura |
Uj,
Pa |
Nov–Feb |
M |
O |
LC |
103 |
Little Stint Calidris
minuta |
Uj,
Ma, Pa, Pi |
Oct–Mar |
M |
F |
LC |
104 |
Temminck's
Stint Calidris temminckii |
Uj, Bh |
Jan–Feb |
M |
O |
LC |
|
Sturnidae |
|
|
|
|
|
105 |
Rosy Starling Pastor roseus |
Uj, Bh, Pa |
Dec–Feb |
M |
F |
LC |
106 |
Brahminy Starling Sturnia pagodarum |
Uj,
Ma, Pa, Ra |
Jan–Dec |
R |
C |
LC |
|
Threskiornithidae |
|
|
|
|
|
107 |
Black-headed Ibis Threskiornis melanocephalus |
Uj, Bh, Ma, Pa |
Sep–Oct |
R |
F |
NT |
108 |
Glossy Ibis Plegadis
falcinellus |
Uj, Bh, Ma, Pa |
Oct–Jan |
M |
O |
LC |
109 |
Indian Black Ibis Pseudibis papillosa |
Uj, Bh, Ma, Pa, Pi |
Jan–Dec |
R |
F |
LC |
110 |
Eurasian Spoonbill Platalea leucorodia |
Uj, Bh, Pa |
Jan–Dec |
R |
F |
LC |
Uj—Ujjani | Bh—Bhadalwadi | Ma—Madanwadi | Pa—Palasdev |
Pi—Pimple | Ra—Ravangaon | R—Resident | M—Migratory |
LC—Least Concerned | NT—Near Threatened | VU—Vulnerable | A—Abundant | C—Common
| F—Frequent | O—Occasional | R—Rare.
For
figures & image - - click here
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