Journal of Threatened Taxa |
www.threatenedtaxa.org | 26 July 2023 | 15(7): 23610–23614
ISSN 0974-7907
(Online) | ISSN 0974-7893 (Print)
https://doi.org/10.11609/jott.8460.15.7.23610-23614
#8460 | Received 29 March 2023 | Final received 08 May 2023 | Finally accepted
05 July 2023
Powerline pylons: an unusual
nesting success of White-bellied Sea-Eagle Haliaeetus
leucogaster (Gmelin,
1788) (Aves: Accipitriformes: Accipitridae)
from Ramanathapuram, southeastern coast of India
H. Byju
1, N. Raveendran 2 & A.J. Mathiyazhagan
3
1 Centre of Advanced Study in
Marine Biology, Annamalai University, Parangipettai,
Tamil Nadu 608502, India.
2 Iragukal Amritha
Nature Trust, 61, Ramachandra Thadaga Street, Thirumangalam, Madurai, Tamil Nadu 625706, India.
3 5/1 Sathya Sai Nagar, Opposite to
Sai Baba Temple, Madurai, Tamil Nadu 625003, India.
1 byjuhi@gmail.com (corresponding
author), 2 Iant.ravee@gmail.com, 3 mathiazhagan.photos@gmail.com
Editor: Anonymity requested. Date of publication: 26 July 2023 (online &
print)
Citation: Byju, H., N. Raveendran & A.J. Mathiyazhagan (2023). Powerline pylons: an unusual nesting success
of White-bellied Sea-Eagle Haliaeetus
leucogaster (Gmelin,
1788) (Aves: Accipitriformes: Accipitridae)
from Ramanathapuram, southeastern coast of India. Journal
of Threatened Taxa 15(7): 23610–23614. https://doi.org/10.11609/jott.8460.15.7.23610-23614
Copyright: © Byju et al. 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: None.
Competing interests: The authors declare no competing interests.
Acknowledgements: Our sincere gratitude to Somu Prasad and his
team of Keelakarai Range of Ramanathapuram
forest division for logistical support during our field visits. We also thank
Kishore. R for helping with the map.
The
White-bellied Sea-Eagle (WBSE) Haliaeetus leucogaster (Gmelin, 1788) is
a resident raptor belonging to the family Accipitridae.
It has a wide distribution range on the sea coast of India from about Mumbai,
south to the eastern coast of Bangladesh, and Sri Lanka in southern Asia (del Hoyo et al. 1994), through all coastal southeastern Asia,
including Burma, Thailand, Malaysia, Indonesia, Indochina, the main and
offshore islands of the Philippines, and southern China, including Hong Kong,
Hainan, and Fuzhou, eastwards through New Guinea & the Bismarck Archipelago,
and Australia. In the northern Solomons, they are
restricted to the Nissan Island (Strange 2000; Ferguson-Lees et al. 2001).
According to the IUCN Red List, it is categorized as ‘Least Concern’ (IUCN
2022).
The WBSE is
occasionally seen in inland waters along tidal rivers and in freshwater lakes
(Ali & Ripley 1987). It feeds mainly on sea snakes and fish. WBSE builds
nests near the seacoast, tidal creeks, and estuaries. This diurnal monogamous
bird of prey occupies the same localities for several years in succession and
nests in tall trees (Ali 1996). Nesting of WBSE is reported from trees like
Mango Mangifera indica,
Casuarina equisetifolia, Banyan Ficus bengalensis,
Fig Ficus religiosa,
Coconut Palm Cocos nucifera, Tamarind Tamarindus
indica, Sterculia
foetida, Terminalia paniculata,
Devil’s Tree Alstonia scholaris,
and Baheda Terminalia bellirica
(Ali 1996; Neema et al. 2021). On the eastern
coast of India, nesting in trees are recorded at Bhitarkanika
(Gopi & Pandav 2006; Palei
et al. 2014), Chilika Lake, and Konark Balukhanda Wildlife Sanctuary (Rahmani
& Nair 2012). On the western coast of India, tree nesting is recorded from
Raigad, Ratnagiri, and Sindhudurg districts of Maharashtra (Katdare
& Mone 2003; Katdare et
al. 2004), and the Netrani Islands of Karnataka (Pande et al. 2011).
Observations
The nesting
observations were conducted from November 2022 to March 2023. We used
binoculars and Canon DSLR cameras with telephoto lenses for observation and
pictures. The visual surveys were carried out for recording parameters like:
(1) the height of the power line tower, (2) height of the nest from the ground,
(3) the width of the artificial structures, and (4) the distance from the sea
(Azman et al. 2013).
On 24
November 2022, during one of our routine shorebirds monitoring studies in Ramanathapuram, we observed a large nest on a powerline
pylon near the rainwater storage area of Pudumadam
(9.289035° N, 78.998988° E) (Figure 1).
This storage area was nearly full last year and almost dried up this year. As
we passed the first pylon to the next one, we saw another nest of similar size,
which made us stop and check the nest from a better position. We observed the
presence of WBSEs sitting on the edge of the nest on the first pylon. As we
scanned the adjacent pylons, we also found a third nest on the third pylon.
Each pylon was at a distance of 100 m from the other (Image 1). These pylons
were on the paddy fields adjacent to the rainwater storage area. WBSEs are reported
to nest on power poles and transmission towers in Australia and Thailand by
birdwatchers. In India, WBSE nesting on a telecommunications tower was reported
from Andhra Pradesh (Narayana & Rao 2019).
The height
of the nest in the pylon was approximately 18 m (60 ft). The base width of the
pylon structure was 180 cm (6 ft). The nest was about 145 m (4 ft) wide (Image
2). The nest is a large deep bowl constructed of thick sticks, twigs, and
branches and lined with materials such as grass, seaweed, or green leaves
(Image 3). The nesting location was at approximately 2 km aerially from the
sea. We maintained a safe distance of about 100 m on the first observation day.
Then one adult bird moved away from the nest in the evening. One stayed back in
the nest, and the other did not return till dark.
On our
subsequent visits on 24-–26 December, we observed an incubating adult on the
nest on the first pylon. We also found a fourth nest on another pylon (the
fourth one) which was absent during the previous observations. Only one nest
among the four was utilized by the WBSEs for incubation. False nesting among
WBSEs is not reported elsewhere, so this could either be a false nesting since
the fourth nest was found during the later observations or the abandoned nests of
previous years. The adult male usually visited the nest during the sunrise. As
soon as this happened, the incubating adult bird slowly got up and stretched
its wings and started flying and soared for about an hour, either alone or with
the other adult bird, and returned to the nest. On 6–7 January 2023, we noticed
the incubation by an adult bird, and the other adult was not seen till evening.
The male bird while reaching the nest, stayed on the edges of the large nest,
while the female continued to incubate the eggs (Image 4).
The
adjacent wetland had more than 50 Brahminy Kite, Black Kite, and a few feral
dogs (Image 5). This place was used as a dumping yard for chicken waste
(poultry) (Image 6). Crows were regularly sighted in the vicinity of the WBSE nest,
often disturbing and chasing one of the adult WBSE (Image 7). During our
observation on 30 January 2023, both adults flew for a few minutes but stayed
close to the nests. A few crows sat on the edges of the nest (Image 8) and the
WBSEs chased them away. The adult female bird incubated almost throughout the
day time. The male often stayed in nearby palm trees and kept a watch on the
nest and often chased away nest approaching Brahminy Kites and Black Kites. On
16 February 2023, we observed the presence of two chicks in the nest (Image 9).
One was smaller compared to the other chick. The male WBSE brought fish to the
nest (Image 10). We also recorded the
left-over fish skeletons beneath the nest (Image 11). At times, the fish were
taken to the adjacent nest in another nearby pylon and eaten there too.
Sometimes, the adult WBSE chased Brahminy Kite and snatched chicken waste from
it and brought to the nest for the chicks to feed on. Black Drongo
had a good relationship with the WBSE. They were present most of the time on
the first and second layers of the pylon and never disturbed the nesting
bird.
The
breeding season of the WBSEs varies according to location. It occurs in the dry
season in Papua New Guinea and from June to August in Australia. According to
Ali & Ripley (1974), WBSEs are known to breed from October to January.
However, in the Ratnagiri district, nest building occurred from mid-September
to January, and chicks were found in the nest by the end of March (Neema et al. 2021). This phenomenon has been documented in
more than 70 raptor species worldwide (Hunting 2002; Lehman et al. 2007).
Several species of birds are known to use pylons and towers for nesting,
perching, and roosting options (Morelli et al. 2014). APLIC (2006) mentions 27
species. Among the bird families, birds of prey are among the groups that are
most seriously affected by electrocution (Ellis et al.2009). Habitat
destruction represents the most significant threat to the species, as it has
resulted in the direct loss of nesting sites and has caused birds to nest in
suboptimal habitat types where breeding success can be reduced (Bilney & Emison 1983).
Conclusion
Due to a
lack of suitable nesting sites and trees, the WBSE has chosen power line towers
for nesting, which are approximately 2 km away from the sea. This helps the
bird conveniently scan the marine area for food. It is important to note
that the use of man-made structures as nesting sites by the WBSE can pose both
risks and benefits to eagles and humans. As a result, careful management and
monitoring of these man-made nesting sites are critical to the safety of both
eagles and human communities.
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