Journal of Threatened
Taxa | www.threatenedtaxa.org | 26 June 2026 | 18(6): 29085–29092
ISSN 0974-7907 (Online) | ISSN 0974-7893 (Print)
https://doi.org/10.11609/jott.10386.18.6.29085-29092
#10386 | Received 09 January 2026 | Final received 01 May 2026| Finally
accepted 02 June 2026
Lotus Nelumbo
cultivations of Beehama Ganderbal
offer novel habitats for diversity and seasonal variation of wetland birds
Sheikh Tanveer Salam 1,
Fayaz Ahmad Ahanger 2 &
Showkat Ahmad Wani
3
1,2,3 Department of Zoology, Government
Degree College Ganderbal, Jammu & Kashmir 191201,
India.
3 Department of Zoology, Government
Sheikh-Ul-Alam Memorial
Degree College Budgam Jammu & Kashmir191111,
India.
1 sheikhtanveersalam@gmail.com
(corresponding author), 2 ahangerfayaz@gmail.com, 3 drshowkat78@gmail.com
Editor: H. Byju,
Coimbatore, Tamil Nadu, India. Date of publication: 26 June 2026
(online & print)
Citation: Salam,
S.T., F.A. Ahanger & S.A. Wani
(2026).
Lotus Nelumbo cultivations of Beehama Ganderbal offer novel
habitats for diversity and seasonal variation of wetland birds. Journal of Threatened Taxa 18(6): 29085–29092. https://doi.org/10.11609/jott.10386.18.6.29085-29092
Copyright: © Salam et al. 2026. 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: None.
Competing interests: The authors declare no competing interests.
Author details: Sheikh Tanveer Salam is currently working as associate professor of Zoology at Government Degree College Ganderbal with specialization in Avian Parasitology but currently working on avian diversity of different wetlands of Kashmir valley. Fayaz Ahmad Ahanger is working as Assistant Professor of zoology with specialization in wildlife and ornithology. Showkat Ahmad Wani is working as Associate Professor of Zoology with specialization in Medical Parasitology but currently working on wetland ecology.
Author contribution: STS is the main author of the paper who collected the entire data and clicked all the photographs. FAA did the statistical analysis of the paper including applying Shannon Weiner index and Simpson index and SAW accompanied the author for carrying out census of birds in different seasons.
Acknowledgments: The authors express their sincere gratitude to all our affiliated organizations—Government Degree College Ganderbal and Government Sheikh-Ul-Alam Memorial Degree College Budgam for their invaluable support and cooperation
throughout the course of this research work.
Abstract: Conversion of marshy paddy fields
into Nelumbo (lotus) gardens by the farmers of
Beehama Ganderbal, Jammu
& Kashmir has not only increased their livelihood and economy but also
started yielding ecological dividends although unintentionally, because these Nelumbo gardens, along with adjoining Salix cultivations
are now serving as alternative and rich habitats for the thriving of wetland
birds. The present study was designed to assess the wetland bird assemblages in
these artificial Nelumbo gardens to understand
the species composition and richness along with their seasonal variation from
March 2023 to February 2025. The study revealed that these artificial Nelumbo gardens can act as potential alternative
feeding and breeding grounds for the diversity of wetland birds when main
wetlands are shrinking due to anthropogenic activities.
Keywords: Alternate breeding grounds, anthropogenic
activities, artificial garden, bird assemblages, lotus cultivation, marshy
paddy field, species composition, wetland bird diversity.
Introduction
Wetlands are transitional lands
between terrestrial and aquatic ecosystems where the water table is usually at
or near the surface or the land is covered by shallow water (Mitsch & Gosselink 1986).
Wetlands provide a home for a diversity of wildlife such as birds, mammals,
fish, frogs, insects, and plants (Buckton 2007). Thus, wetlands help maintain
biodiversity of flora and fauna. Wetlands are complex and productive ecosystems
that occupy about six per cent of the Earth’s land surface (Maltby & Turner
1983; Maltby 1986; Unni 2002; Thomas et al. 2026).
Hence, wetlands are known as “biological supermarkets” because of the extensive
food chains and rich biodiversity that they support, providing unique habitats
for a wide range of flora and fauna (Mitsch & Gosselink 2000). They are also important habitats for water
birds, which use them for feeding, roosting, nesting and rearing young. In
addition to being the most productive ecosystems,
wetlands play a vital role in flood control, aquifer recharge, nutrient absorption
and erosion control.
Lotus or golden lotus is a
perennial plant that grows in lakes in many parts of the world, including
Kashmir. In Kashmir, it naturally grows in Dal, Wular,
Manasbal, and Anchar lakes.
As the rhizome of the plant is used as a delicacy and food by the people of the
valley, it is an economically important plant. So, people have also started
cultivating it for their livelihood, and the land near lakes and wetlands is
being brought under Nelumbo cultivation. In
summer, these cultivations provide cover, food, and nesting habitat for birds,
while in winter they provide food and open water areas. Hence, these
cultivations attract birds in the summer as well as the winter. These man-made Nelumbo gardens not only provide alternatives for the
cultivation of Nelumbo, reducing the
anthropogenic pressure on the wetlands for harvesting Nelumbo,
but also act as alternative safe feeding and breeding grounds for migratory and
resident aquatic birds. As no study has yet been conducted on the avian diversity
of these habitats, in this present study, an attempt has been made to document
the species richness and diversity of the avifauna of these habitats.
Study area
The present study was carried out
in the lotus (Nelumbo) cultivations of Beehama Ganderbal (34.207o N, 74.78o
E). The study site is located about 18 km north of the capital city Srinagar on
the west side of the Srinagar-Leh Highway at an
altitude of approximately 1,585–1,619 m. The site used to be marshy paddy
fields connected to the Pandach Wetland Reserve,
which were converted into Nelumbo cultivations
by the locals for better economic returns by selling Nelumbo
rhizomes on the National Highway. These cultivations are not only yielding
economic benefits to local farmers but also starting to yield ecological
dividends by acting as alternative feeding and breeding habitats for resident
and migratory wetland birds.
Methods
The study was carried out on
these newly emerging habitats for two years, from May 2023 to April 2025. The
study site is a continuous Nelumbo cultivation
of about 6.89 lac sq ft in area with some patches
filled for residential houses and some patches of deep open waters. The study
area was visited weekly, and the birds were counted in all four seasons, viz.,
Spring (March–May), Summer (June–August), Autumn (September–November), and
Winter (December–February). Therefore, the study site was visited 12 times in
each season. Counting of birds was done using the Nikon binocular (22 x 50) and
employing the point count, flock count, and group count method (Choudhary &
Soni 2023), considering the landscape of the study
site. We selected six vantage points in different cardinal directions of the
study site, spending 5–10 minutes at each point, as this duration maximizes
detection efficiency while minimizing bias (Bonthoux
& Balent 2012) for bird counts. Species were
identified using eBird/Clements Checklist (Clements
et al. 2025), and data were collected species-wise. Surveys were abandoned on
days with rain, snowfall and strong wind (Verner 1985; Bibby et al. 2000).
Surveys were also halted during paddy agricultural disturbance periods, like
one week in April during nursery preparation, one week in June during planting
of saplings and one week in October during harvest. Double-counting was avoided
by recording the birds that flew into and out of the plots during the census.
Birds with fewer than 10 records were categorized as rare, those with 10–50
records as common, and those with more than 50 records as abundant (Bibby et
al. 2000). Total abundance (number of birds observed from different counting
points) and mean total abundance (total number of birds counted divided by
total number of counting points) were also recorded. A checklist of species was
also prepared. Birds were photographed using a Nikon D5600 camera with a
200–500 mm Nikkor lens. The data collected was
compiled in Microsoft Excel. Shannon-Weiner index (H) and Simpson diversity
index (D) were used to evaluate species diversity during different seasons of
the study.
Shannon-Weiner index
H = - Σ pi ln(pi)
where:
Σ: A Greek symbol that means “sum”, ln: Natural log, pi: The
proportion of the entire community made up of species i
Simpson index
Σn (n – 1)
D = 1 – –––––––––
N (N – 1)
Where n = number of individuals
of each species, N = total number of individuals of all species
Results
and Discussion
A total of 71 species of birds
belonging to 12 orders and 29 families were recorded in the present study
(Table 1). Passerines, represented by 35 species, contribute about 49.29% of
the bird diversity of the study area. Of the total diversity, 43.66% (31
species) were summer migrants (SM), followed by 42.25% (30 species) of
residents (R), 11.26% (8 species) of winter migrants (WM) and only 2.81% (2
species) of local altitudinal migrants (LAM). No passage migrant was observed.
Among these, some like Mallard Anas platyrhynchos, Eurasian Teal Anas
crecca, Northern Shoveller
Anas clypeata, Common Moorhen Gallinula chloropus,
Grey-headed Swamphen Porphyrio
poliocephalus and Little Grebe Tachybaptus ruficollis
are typical marsh-dwelling species, while some upland birds like Indian Pond
Heron Ardeola grayii,
Black-Crowned Night Heron Nycticorax nycticorax, Little Bittern Ixobrychus
minutus, Eurasian Collared Dove Streptopelia decaocto,
European Roller Coracias garrulus, etc., spend a great deal of their time in the
lake for feeding but nest on adjoining trees and shrubs. A total of 592 species
of resident and non-resident birds have been reported from Jammu & Kashmir
(Kichloo et al. 2024). About 92 species have been recorded
from the wetlands of Kashmir (Holmes & Parr 1988; Ahangar
2008). The present study clearly revealed that a good number of species are
visiting these newly created habitats, thereby providing a ray of hope that
these Nelumbo gardens can act as alternative
feeding and breeding sites for different types of birds, besides providing
economic benefits to the locals. The
areas with floating vegetation like Trapa natans, Nymphoides
sp., and Potomogeton were used for nesting by
birds like Little Grebe and Whiskered Tern Chlidonias
hybrida. The emergent macrophytic
vegetation, Phragmites communis, Typha angustata, Scirpus palustis, Sparganium
ramosum, and Butomus
umbellatus were used for nesting by birds like
Mallard, Little Bittern, Indian Great Reed-Warbler Acrocephalus
stentoreus, Common Moorhen and Wagtails, while
the peripheral trees served as the nesting sites for a number of upland species
like Herons, Doves, Rollers, Indian Golden Oriole Oriolus
oriolus, Rufous-Backed Shrike Lanius
schach, and Indian Paradise Flycatcher Terpsiphone paradisi. These
findings are consistent with earlier studies from the region (Bates &
Lowther 1952; Ali 2002; Ahanger 2008; Fazili et al. 2017).
The diversity of birds assembling
at the Nelumbo gardens varied among different
seasons. Diversity was found to be relatively higher during early Spring (H =
3.961; D = 0.9586) and late Winter (H = 3.811; D = 0.9572), followed by Summer
(H = 3.376; D = 0.8706), and the least diversity was reported in Autumn (H =
3.267; D = 0.8281). The highest diversity during spring can be
attributed to the assemblage of early summer migrants and already staying late
winter migrants, besides the resident species, increasing the diversity of
avifauna during Spring. The reason for the lowest diversity during autumn can
be due to the presence of only residents in these sites during this period
(Table 2) because during Autumn, summer migrants migrate to their feeding
grounds, and most of the resident birds also move towards residential areas and
nearby paddy fields (Byju et al. 2023). Besides this,
there is a huge disturbance to birds during late autumn and early winter due to
intensive harvesting of Nelumbo stems locally
called Nadru for selling them on small stalls
at the adjoining Srinagar-Leh National Highway. The
observations in the present study are in line with earlier observations from
the wetlands of the adjoining states (Choudhary & Soni
2023).
With respect to abundance, 18
species (25.35%) were abundant, 22 species (30.98%) were common, and 31 species
were rare (43.66%). The maximum total abundance (1908 individuals) was recorded
in the winter season, with a mean abundance of 477 individuals. The minimum
total abundance (184 individuals) was recorded in the autumn season with a mean
abundance of 46 individuals.
These newly emerging habitats are
facing serious anthropogenic threats due to the filling of these wetlands for
making residential plots. Besides this, demarcations of the different plots by
the owners using nets threaten and repel the birds. Harvesting of grass along
footpaths within these Nelumbo gardens by the
local women for cattle fodder may significantly disturb avifaunal communities inhabiting
these wetlands and can lead to degradation of nesting habitats.
Conclusion
Conversion of less productive
full-time water-logged paddy fields into productive Nelumbo
(lotus) gardens, as revealed from the survey of the households involved in
this venture, represents a sustainable land-use alternative with significant
economic and ecological advantages. Economically, this practice offers higher
and more stable returns compared to conventional paddy cultivation under
water-logged conditions, thereby improving livelihood opportunities for local
farmers by selling the rhizomes of the lotus on the adjacent Srinagar-Leh National Highway. Ecologically, these sites are
emerging as structurally diverse wetland habitats that support rich
biodiversity by attracting a wide range of resident and migratory bird species
for feeding, breeding and shelter. A good avifaunal diversity observed at the
study site underscores the role of Nelumbo gardens
in enhancing ecosystem services, and this land use-transformation aligns
agricultural productivity with wetland conservation goals, suggesting that Nelumbo-based systems can serve as a viable
mode for sustainable management of water-logged agricultural landscapes. These
systems can be managed to optimize both livelihood benefits and biodiversity
outcomes through an integrated, eco-sensitive approach by engaging local
communities, particularly women, for promoting sustainable harvesting by
providing incentives for conservation-friendly practices. Identify and mapping
of key nesting and roosting sites to establish temporary exclusion zones during
breeding periods. Maintain optimal and stable water levels to support both Nelumbo growth and avifaunal requirements,
and retain patches of open water interspersed with Nelumbo
to support diverse bird guilds like waders, dabblers and diving birds.
Encourage a mosaic of native macrophytes alongside Nelumbo
to increase structural complexity and food availability for sustaining higher
bird diversity. There is an immediate need to integrate these systems into
wetland conservation policies and rural development schemes to ensure
institutional backing for sustainable management.
Table 1. Checklist of birds
identified in the study.
|
Order |
Family |
Common name |
Scientific name |
Status* |
Abundance |
|
Podicipediformes |
Podicipedidae |
Little Grebe |
Tachybaptus ruficollis Pallas, 1764 |
R |
Common |
|
Ciconiiformes |
Ardeidae |
Little Egret |
Egretta garzetta Linnaeus, 1766 |
R |
Common |
|
Indian Pond Heron |
Ardeola grayii Sykes, 1832 |
R |
Abundant |
||
|
Black-crowned Night Heron |
Nycticorax nycticorax Linnaeus, 1758 |
R |
Rare |
||
|
Little Bittern |
Ixobrychus minutus Linnaeus, 1766 |
SM |
Rare |
||
|
Anseriformes |
Anatidae |
Mallard |
Anas platyrhynchos Linnaeus, 1758 |
WM |
Abundant |
|
Northern Shoveler
|
Anas clypeata Linnaeus, 1758 |
WM |
Abundant |
||
|
Eurasian Teal |
Anas crecca Linnaeus, 1758 |
WM |
Abundant |
||
|
Falconiformes |
Accipitridae |
Black Kite |
Milvus migrans Boddaert, 1783 |
R |
Abundant |
|
Common Buzzard |
Buteo buteo Linnaeus, 1758 |
WM |
Rare |
||
|
Long-legged Buzzard |
Buteo rufinus Cretzschmar, 1827 |
WM |
Rare |
||
|
Eurasian Sparrowhawk |
Accipiter nisus Linnaeus, 1758 |
WM |
Rare |
||
|
Western Marsh Harrier |
Circus aeruginosus
(Linnaeus, 1758) |
WM |
Rare |
||
|
Gruiformes |
Rallidae |
Ruddy-breasted Crake |
Porzana fusca Linnaeus, 1766 |
SM |
Rare |
|
Grey-headed Swamphen |
Porphyrio poliocephalus Linnaeus, 1758 |
R |
Abundant |
||
|
Common Moorhen |
Gallinula chloropus Linnaeus, 1758 |
R |
Abundant |
||
|
Common Coot |
Fulica atra Linnaeus, 1758 |
WM |
Abundant |
||
|
Charadriiformes |
Scolopacidae |
Common Sandpiper |
Actitis hypoleucos Linnaeus, 1758 |
R |
Common |
|
Green Sandpiper |
Tringa ochropus Linnaeus, 1758 |
R |
Common |
||
|
Laridae |
Whiskered Tern |
Chlidonias hybrida Pallas, 1811 |
SM |
Rare |
|
|
Charadriidae |
Red wattled
Lapwing |
Vanellus indicus (Boddaert, 1783) |
SM |
Rare |
|
|
Northern Lapwing |
Vanellus vanellus (Linnaeus, 1758) |
SM |
Rare |
||
|
Columbiformes |
Columbidae |
Blue Rock Pigeon |
Columba livia Gmelin, 1789 |
R |
Abundant |
|
Eurasian Collared-Dove |
Streptopelia decaocto Frivaldszky, 1838 |
SM |
Common |
||
|
Oriental Turtle-Dove |
Streptopelia orientalis (Latham, 1790) |
SM |
Rare |
||
|
Psittaciformes |
Psittacidae |
Rose-ringed Parakeet |
Psittacula krameri Scopoli, 1769 |
R |
Rare |
|
Cuculiformes |
Cuculidae |
Common Cuckoo |
Cuculus canorus Linnaeus, 1758 |
SM |
Rare |
|
Pied Crested Cuckoo |
Clamator jacobinus Boddaert, 1783 |
SM |
Rare |
||
|
Coraciiformes |
Alcedinidae |
Common Kingfisher |
Alcedo atthis Linnaeus, 1758 |
R |
Abundant |
|
White-breasted Kingfisher |
Halcyon smyrnensis Linnaeus, 1758 |
R |
Abundant |
||
|
Lesser Pied Kingfisher |
Ceryle rudis Linnaeus, 1758 |
R |
Rare |
||
|
Coraciidae |
European Roller |
Coracias garrulus Linnaeus, 1758 |
SM |
Rare |
|
|
Upupidae |
Common Hoopoe |
Upupa epops Linnaeus, 1758 |
SM |
Common |
|
|
Piciformes |
Picidae |
Himalayan Pied Woodpecker |
Dendrocopos himalayensis Jardine & Selby, 1831 |
R |
Common |
|
Brown-fronted Pied
Woodpecker |
Dendrocopos auriceps Vigors, 1831 |
R |
Rare |
||
|
Large Scaly-bellied Green
Woodpecker |
Picus squamatus Vigors, 1831 |
R |
Rare |
||
|
Passeriformes |
Passeridae |
House Sparrow |
Passer domesticus Linnaeus, 1758 |
R |
Abundant |
|
Hirundinidae |
Common Swallow |
Hirundo rustica Linnaeus, 1758 |
SM |
Common |
|
|
Motacillidae |
White Wagtail |
Motacilla alba Linnaeus, 1758 |
R |
Common |
|
|
Citrine Wagtail |
Motacilla citreola Pallas, 1776 |
R |
Common |
||
|
Grey Wagtail |
Motacilla cinerea Tunstall, 1771 |
R |
Common |
||
|
Rosy Pipit |
Anthus roseatus Blyth, 1847 |
SM |
Rare |
||
|
Water Pipit |
Anthus spinoletta Linnaeus, 1758 |
SM |
Rare |
||
|
Oriental Tree Pipit |
Anthus hodgsoni Richmond, 1907 |
SM |
Rare |
||
|
Campephagidae |
Long-tailed Minivet |
Pericrocotus ethologus Bangs & Phillips, 1914 |
SM |
Rare |
|
|
Passeriformes |
Pycnonotidae |
Himalayan Bulbul |
Pycnonotus leucogenys Gray, 1835 |
R |
Abundant |
|
Black Bulbul |
Hypsipetes leucocephalus P.L.S. Muller, 1776 |
LAM |
Common |
||
|
Laniidae |
Rufous-backed Shrike |
Lanius schach Linnaeus, 1758 |
SM |
Common |
|
|
Troglodytidae |
Winter Wren |
Troglodytes troglodytes Linnaeus, 1758 |
LAM |
Rare |
|
|
Muscicapidae |
Blue Whistling-Thrush |
Myiophonus caeruleus Scopoli, 1786 |
R |
Abundant |
|
|
Tickell’s Thrush |
Turdus unicolor Tickell, 1833 |
SM |
Rare |
||
|
Spotted Forktail
|
Enicurus maculatus Vigors, 1831 |
SM |
Rare |
||
|
Streaked Laughingthrush |
Garrulax lineatus Vigors, 1831 |
SM |
Common |
||
|
Indian Great Reed-Warbler |
Acrocephalus stentoreus Hemprich & Ehrenberg,
1833 |
SM |
Common |
||
|
Indian Paradise Flycatcher |
Terpsiphone paradisi Linnaeus, 1758 |
SM |
Rare |
||
|
Siberian Stonechat |
Saxicola maurus Linnaeus, 1766 |
SM |
Common |
||
|
Common Chiffchaff |
Phylloscopus collybita Vieillot, 1817 |
SM |
Common |
||
|
Lemon-rumped
Warbler |
Phylloscopus chloronotus G.R. Gray & J.E. Gray, 1846 |
SM |
Rare |
||
|
Hume’s Warbler |
Phylloscopus humei (Brooks, 1878) |
SM |
Rare |
||
|
Paridae |
Coal Tit |
Parus ater Linnaeus, 1758 |
SM |
Rare |
|
|
Great Tit |
Parus major Linnaeus, 1758 |
R |
Common |
||
|
Certhiidae |
Bar-tailed Tree-Creeper |
Certhia himalayana Vigors, 1832 |
R |
Rare |
|
|
Sturnidae |
Common Starling |
Sturnus vulgaris Linnaeus, 1758 |
SM |
Common |
|
|
Common Myna |
Acridotheres tristis Linnaeus, 1766 |
R |
Abundant |
||
|
Oriolidae |
Indian Golden Oriole |
Oriolus oriolus Linnaeus, 1758 |
SM |
Rare |
|
|
Dicruridae |
Black Drongo |
Dicrurus macrocercus Vieillot, 1817 |
SM |
Common |
|
|
Ashy Drongo |
Dicrurus leucophaeus Vieillot, 1817 |
SM |
Common |
||
|
Corvidae |
Yellow-billed Blue Magpie |
Urocissa flavirostris (Blyth, 1846) |
R |
Abundant |
|
|
Eurasian Jackdaw |
Corvus monedula Linnaeus, 1758 |
R |
Abundant |
||
|
House Crow |
Corvus splendens Vieillot, 1817 |
R |
Abundant |
||
|
Jungle Crow |
Corvus macrorhynchos Wagler,
1827 |
R |
Common |
*—Each species was classified
according to its residential status, R—Residents | SM—Summer migrants |
WM—Winter migrants | LAM—Local altitudinal migrants, based on field evidence
and corroborated with authentic online datasets (Bates & Lowther 1952;
Swati & Swati 2026).
Table 2. Avian diversity in different seasons of the study.
|
Diversity index |
Spring (Mar–May) |
Summer (Jun–Aug) |
Autumn (Sep–Nov) |
Winter (Dec–Feb) |
|
Shannon-Weiner index (H) |
3.961 |
3.376 |
3.267 |
3.811 |
|
Simpson index (D) |
0.9586 |
0.8706 |
0.8281 |
0.9572 |
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