Journal of Threatened Taxa |
www.threatenedtaxa.org | 26 March 2023 | 15(3): 22823–22833
ISSN 0974-7907
(Online) | ISSN 0974-7893 (Print)
https://doi.org/10.11609/jott.8290.15.3.22823-22833
#8290 | Received 29
November 2022 | Final received 22 January 2023 | Finally accepted 26 February
2023
Habitats and nesting habits of
Streaked Weaver Ploceus manyar
in select wetlands in the northern districts of Tamil Nadu, India
M. Pandian
No. F1901, Taisha, Natesan Nagar West, Virugambakkam,
Chennai, Tamil Nadu 600092, India.
Abstract: The habitats and nesting habits of Streaked
Weaver Ploceus manyar
was studied in the Narrow Leaf Cattail Typha angustifolia (Typhaceae) wetlands in Ranipet,
Kancheepuram, and Viluppuram districts of northern
Tamil Nadu. A total of 349 nests, in various developmental stages, in 24
colonies and of 536 adult individuals were enumerated. Of these 349 nests, 43
nests were in wad stage, 28 in ring stage, 123 in helmet stage, 55
egg-chamber-closed stage, and 100 complete nests including two abnormal nests
were recorded. Streaked Weaver used fibres of T.
angustifolia for building nests. Females were also observed to be engaged
in nest construction, while males placed blobs of cow dung on the inner or both
walls of helmet stage nests before pairing with females; 88.7% helmet stage
nests had deposition of cow dung on their inner walls and the remaining 11.3%
nests had no such deposits. In 59% nests the entrance tubes were found facing
east. They showed communal foraging and the flock size ranged from 50─80 birds.
No antagonistic interactions were observed between Streaked Weavers and other
species over sharing of common perching sites and foraging grounds. Harvesting
of nest-supporting reeds and sightings of avian predators, such as House Crow Corvus splendens,
Large-billed Crow Corvus macrorhynchos, and Rufous Treepie Dendocitta
vagabunda near nest colonies may pose threats to
Streaked Weavers.
Keywords: Abnormal nests, communal
foraging, deposition of cow dung, nest colonies, nest orientation, Typha
angustifolia.
Editor: H. Byju,
Coimbatore, Tamil Nadu, India. Date
of publication: 26 March 2023 (online & print)
Citation: Pandian, M. (2023). Habitats and nesting habits of Streaked Weaver Ploceus manyar in
select wetlands in the northern districts of Tamil Nadu, India. Journal of Threatened Taxa 15(3): 22823–22833. https://doi.org/10.11609/jott.8290.15.3.22823-22833
Copyright: © Pandian 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 author declares no competing interests.
Author details: M. Pandian has completed MSc, PhD, in botany and BLIS from University of Madras and Bachelor of Education (B.Ed.) from Annamalai University, Chidambaram and now serves in Tamil Nadu Police Department. His area of interest is ecology and nesting biology of birds and published a few papers on House Sparrows, Baya Weavers, Streaked Weaver and Black-breasted Weaver, Grey Francolins, Indian Flying Fox, munias and Ring-necked Parakeets.
Acknowledgements: I thank D. Balaji (Mailam), and K. Sriram (Rettananai)
for assistance in collection of data and photography, A. Giridharan
(Minnal) and P. Poornima (Odisha) for data analysis /
preparation of study area maps.
INTRODUCTION
Ploceidae is a family of Passerine birds,
many of which are called weavers. The family is believed to have originated in
the mid-Miocene (De Silva et al. 2017). The group comprises a total of 116
species in 15–17 genera (Clements et al. 2022) and is well known for their
intriguing and dramatic variation in behaviour, nest
structure, and plumage coloration (Collias & Collias 1964). The Afro-Asian region harbours
64 species of weavers (Dickinson & Christidis
2014). Four species alone occur in India: Baya Weaver
Ploceus philippinus,
Black-breasted Weaver P. benghalensis,
Streaked Weaver P. manyar, and Finn’s Weaver
P. megarhynchus (Ali & Ripley 1987). Though
the Streaked Weaver occurs widely in India, its nesting colonies are scattered
across the peninsular region (Rasmussen & Anderton 2005). Detailed accounts
of its breeding biology were studied in Kumaon Terai (Ambedkar 1972), Wazirabad, Delhi (Prakash et al.
2020), and Veedur wetlands, Tamil Nadu (Pandian
2022). The other published works on the Streaked Weaver are either anecdotal
accounts of its natural history, e.g., roosting behaviour
(Dhindsa & Toor 1981),
crop damage (Dhindsa 1982), causes of nest
destruction (Sharma 1997), and on nesting in Ipomoea reed beds (Panwar
et al. 2020); or records in regional checklists, e.g., Dharmapuri (Vasanth 1990), Coringa Wildlife Sanctuary (Srinivasulu
et al. 2000), Pallikaranai (Raj et al. 2010),
Mayiladuthurai (Ali et al. 2011), Kalpakkam (Hussain
et al. 2011), Tiruchirappalli (Siva & Neelanarayanan
2017), and Chengalpet (Nagarajan 2021).
The present study documents the
various habitats and nesting habits of the Streaked Weaver in the T.
angustifolia reeds in northern Tamil Nadu. The aim of this study was to
investigate the habitats, nesting behaviours, and
probable threats to their populations.
MATERIALS AND METHODS
Study area
The present
study was carried out in the selected reeds covered wetlands providing definite
habitats to Streaked Weavers in Ranipet, Kancheepuran, and Viluppuram
districts of northeastern Tamil Nadu (Figure 1). These three districts cover an
area of c. 7600 km2 with a human population of c. 44,00,000.
Monsoon-dependent Palar, Kosasthalaiyar,
Ponnaiyar, Thenpennai, Varaha, and Thondi rivers pass
through these districts. The reeds at the study sites comprise Narrow Leaf
Cattail Typha angustifolia, spread over c. 4 ha. Apart from that Chrysopogon zizanioides
and Phragmites spp. occur abundantly in the study sites. Agriculture is
the primary occupation in the district. The major crops of the area are Rice Oryza
sativa, Jowar Sorghum bicolor, Pearl Millet Pennisetum
glaucum, Finger Millet Eleusine
coracana, Sugarcane Saccharum
officinarum, and pulses such as Black Gram Vigna
mungo, Green Gram Vigna radiata, & Pigeon Pea Cajanus cajan.
Monoculture of Casuarina equisetifolia and
cultivation of vegetables & flowers are also common. Temperatures range
from 20─36 oC. The average annual rainfall
is c. 1,000 mm.
METHODS
Data collection
A survey was conducted in the c.
4 ha reed beds situated along the arable lands in three districts. The selected
wetlands in three districts were identified that had a definite history of the
existence of P. manyar populations and their
nests in the previous years. These sites were surveyed between 0600 h and 1800
h during the breeding season from 01 February─15 July 2022. The following
variables were quantified: area of nesting colonies, depth of water (measured
using a bamboo pole), size of nest colonies, number of nests in each colony,
the distance between adjacent nest colonies, number of nests in various
developmental stages, the orientation of nests, and distance between the reeds
& foraging sites, i.e., paddy fields. The communal foraging behaviours, interactions with other species, and threats to
their populations were observed uninterruptedly from a reasonable distance (c.
20 m) through binoculars, without causing disturbance to the birds. The number
of birds was enumerated by following the total count method (Bibby et al.
2000) and analysing photographs taken when the birds
were foraging and perching on nearby plants. Bird census was conducted over
four monthly sessions during the second week of every month, i.e., March–June
2022. The total number of birds is expressed as the highest count of the
session’s total count. Photographic documentation of various developmental
stages of nests and deposition of cow dung on the wall of helmet stage nests
was done. The choices of grains/seeds foraged by the Streaked Weavers were
observed and identified plant species foraged by these birds. The damaged
nests, size of harvested reed areas by humans, and other plants that caused
disturbance to nest colonies were quantified. The sighting of avian predators
in the vicinity of nest colonies were observed and recorded.
Data analysis
After the breeding season was
over and the nests were completely abandoned by the birds, the number of leaves
attached to the roofs of nests, the length, and the diameter of entrance tubes
were measured in 15 nests. The number of nests per colony, the distance between
the nest colonies, and the nearest roads, buildings & electric cables were
measured. Based on these data, bar charts were made. Karl Pearson’s correlation
coefficient (r) test was used to assess the significant relationship
between the height of reeds above water level & the total number of nests
and between the depth of water & the number of nests. No live nest, adult
bird, egg or chick was handled during the study. Locations of the nest colonies
in the reeds were determined using a Garmin Etrex 20x
GPS device. Photographs and videography were made using a Nikon P1000 digital
camera. The collected data were tabulated, analysed,
and shown as a graphical representation.
RESULTS
A total of 349 nests, including
some in various developmental stages in 24 nest colonies, and 536 individuals
of Streaked Weaver were enumerated. Colony size ranged 4─43 nests. Of the 349
nests, 12% nests (n = 43) were in wad stage, 8% in ring stage (n = 28), 35% in
helmet stage (n = 123), 16% in egg-chamber closed stage (n = 55), and 29%
complete nests (n = 100). The size of reeds containing nest colonies varied
from a minimum of 0.04 ha to a maximum of 0.24 ha. The minimum distance between
the adjacent nest colonies was 30 m and the maximum was 70 m. The depth of
water in the wetland also varied. It was shallowest at 0.3 m, and deepest at
1.6 m. Maximum nests (n = 43) was observed on reeds standing in water
containing 30 cm depth, followed by 41 nests on reeds having 120 cm depth, and
33 nests on reeds with 100 cm depth. The height of the reeds above the water
level also varied: minimum of 1.4 m and maximum of 3 m. Maximum nests (n = 271;
77.65%) were enumerated on reeds having height ranges of 1.6 m─2 m (Table 1).
Nest construction and materials
The study revealed that Streaked
Weaver used fibers of T. angustifolia for the construction of nests in
all three districts. Both sexes contributed to nest construction. Males built
nests up to helmet stages and then, after pairing with females, both sexes
collected fibres and continued the building. No other
plant materials were used by the birds for the construction of nests.
Selection of nesting sites and
stages of nest construction
Individuals of male Streaked
Weaver with breeding plumages first appeared on reeds in first week of February
2022. The males visited various leaves, perching during the day on particular
leaves of the T. angustifolia, 1–2 m above the water except for the
duration of forage, but they did not engage in nest construction. From the
second week of February onwards, males brought fibres
from adjacent T. angustifolia and started building wad stage nests (by
tying knots) and later the wad stage nests were developed into various stages
of nests. After selecting a nesting site, a male Streaked Weaver bends and
lowers the distal ends of two T. angustifolia leaves, holding them
together with its toes, and plaits a knot around the leaves with its beak. Once
this initial knot is tied, the male easily pulls down adjacent leaf tips, one
by one and in a similar manner, and makes the basal knot stronger, creating a
wad. The number of leaves attached to each wad nest varies from nest to nest.
Males brought fibres continuously and made the wad
stronger, like an amorphous roof/ceiling-like structure into which they
enmeshed many green leaves. Out of 349 nests observed, only 29 % nests (n =
100) were developed into complete nests including two abnormal nests (bistoried 1+1 type) at the end of the breeding period
(Figure 2) (Table 1). Only females were observed feeding their chicks. On three
occasions, males were carrying the food in their beaks to the nesting colony
but it was not possible to observe whether they entered the nests with food or
not.
The length of the entrance tube
varies from nest to nest and the measurement of entrance tubes of 15 abandoned
nests revealed variations of 9–20 cm in length and 4–5 cm in diameter. The base
of the nests was attached with 30–55 leaves. Apart from leaves, the birds also
enmeshed peduncles with the base of nests (n = 22). The nests did not swing
freely, because they were attached to many leaves of the T. angustifolia.
A nest rarely swung along with the nest-supporting plants, during a gust,
remaining suspended, and static most of the time. The distal ends of entrance
tubes were 0.8—1.5 m above the water’s surface (Figure 3). Pearson’s
correlation coefficient test reveals that there exists no significant
correlation (r = -0.0946) between the height of reeds above water level &
the number of nests and similarly no correlation (r = -02475) exists between
depth of water under the nest colonies & several nests.
Nest Colonies
The size of reed beds containing
nest colonies varied 0.04─0.24 ha. The number of nests per colony also varied
4─43. The distance between adjacent nests ranged 1─4 m. Out of 349 nests
enumerated, maximum nests were observed in the nest ranges 21─30 nests,
followed by 41─43, and 1─10 nests (Table 2; Image 1i).
Preference of Streaked Weaver in
building nests on reeds occurring close to human activities
The study
also tested the relationship between the proximity of roads, buildings,
electric cables, and the selection of nest-supporting plants by individuals of
Streaked Weaver. Three percent of nests (n = 9) occurred within a 25 m radius
from the nearest roads, 33% of nests (n = 116) within a 26─50 m radius, and the
remaining 65% of nests (n = 224) occurred above a 51 m radius from roads. Of
the verified details, 32% of the nests (n = 111) occurred within a 200 m radius
of buildings such as human dwellings, cattle sheds, & motor pump sets in
crop fields, and the remaining 68% of nests (n = 238) occurred above 200 m
radius from buildings; 38% of nests (n = 132) were found within 50 m of
electric cables and the remaining 62% of nests (n = 217) occurred above 50 m
from the nearest power cables (Figure 3─5).
Orientation of nests
Examination of the orientation of
155 nests (egg-chamber closed stage-55 & complete nests-100) on the
nest-supporting plants revealed that 59% of nests (n = 91) were oriented east
facing the rising sun, while 12% of nests (n = 18) were oriented the west, 25%
nests towards (n = 39) north and 5% nests (n = 7) were found facing south. The
study reveals that entrance tubes of maximum nests were found facing the east
(Figure 6).
Deposition of cow dung
The males have the habit of
smudging cow dung on the inner walls of helmet stage nests before pairing with
a female. Out of 80 helmet stage nests that were studied, 88.7% helmet stage
nests (n = 71) had a thick layer of dung on their inner walls (Image 2a),
whereas the remaining 11.3% nests (n = 9) had no deposits of cow dung. Abnormal
deposits of dung were found in seven nests, where dung had been plastered on
both, inner and outer surfaces. Males had deposited cow dung abnormally like
horn-shaped structures on the outer walls of these nests (Image 2b). No females
were observed in the vicinity of nest colonies or seen carrying cow dung to the
nests.
Communal foraging
The study revealed that all the
nest colonies were surrounded by paddy crops (Oryza sativa: Poaceae) that occurred 25─800 m distance from the nest
colonies. The Streaked Weaver always moved in flocks and the flock
varied in size from 50─80 birds. The flocks contained a few individuals of
other species, such as Baya Weaver P. philippinus, Black-breasted Weaver P. benghalensis, Tricolored Munia Lonchura
malacca, White-rumped
Munia L. striata, and Indian Silverbill Euodice malabarica. They strictly followed communal foraging.
They forage on paddy when it is at the milky and unripe seed stage. They also
perched on the spikes of T. angustifolia, Setaria
pallide-fusca, and Paspalidium
geminatum and consumed their unripe seeds. The
individuals of Streaked Weaver coexisted with the aforesaid other bird
species without any competition over sharing of common perching sites or food
grains while foraging.
Threats
The study reveals that out of c.
4 ha of reeds in the study sites, c. 700 m2 reeds were harvested by
local villagers during the current breeding period for making mats and ropes.
It was observed that 21 nests of various developmental stages (wad stage 7,
ring stage 11, and helmet stage 1) were abandoned by the birds as the nearby reeds
were harvested resulting in the exposure of nests to the outside. The birds
might have abandoned those nests due to apprehension of movements of human
beings, cattle, and exposure of nests to outside/predators. Birds had abandoned
12 nests (wad 8 and helmets 6) which were found enmeshed in the angiosperm
climber Oxystelma esculentum
and angiosperm parasite Cassytha filiformis which thickly covered and caused fallen down
of T. angustifolia reeds. One complete nest was found torn probably due
to the predators. Predatory birds, such as House Crow Corvus
splendens, Large-billed Crow Corvus
macrorhynchos, and Rufous Treepie Dendrocitta vagabunda
were sighted (n = 59) in the vicinity of nesting colonies during the study
period (Image 3; Table 3).
DISCUSSION
Many authors had previously
studied the breeding periods of the Streaked Weaver. The breeding period was
completed by the end of May in Dharmapuri District (Vasanth 1990), between
February and June in Viluppuram, Tamil Nadu (Pandian
2022), and between May and July 2012 in Wazirabad (Prakash et al. 2020). But in
the present study, breeding occurred between February and July as stated by
Prakash et al. (2020) and Pandian (2022). Streaked Weavers used fibres from Phragmites, Typha, and Vetiveria in Wazirabad (Prakash et al. 2020).
In the present study, the birds used fibres from
leaves of T. angustifolia only, and not of Phragmites spp. or Vetiveria spp., as stated by Prakash et al. (2020).
Though Chrysopogon (=Vetiveria)
zizanioides and Phragmites spp. occur
abundantly in the study sites, the birds did not pluck fibres
from these plants, and the reasons for not selecting these plant species are
not known and hence, it requires further studies. They attached many leaves of T.
angustifolia with an initial knot (wad stage) and formed a strong
roof/ceiling of the nests (Ambedkar 1972; Prakash et al. 2020; Pandian 2022).
The present study revealed that a minimum of 30 and a maximum of 55 leaves
including peduncle of the inflorescence of T. angustifolia were found
attached to the base of the nest, corroborating the findings of Ambedkar
(1972), and Prakash et al. (2020), and Pandian (2022). In Gadharpur, Uttarakhand, the number of nests per colony
varied from 12─20 nests, and the largest colony contained 60 nests (Ambedkar
1972). But Prakash et al. (2020) recorded only a maximum of 11 nests per colony
in Wazirabad. The present study revealed that the nest colonies contained 4─43
nests, partly corroborating the observations of Ambedkar (1972). The study
revealed that maximum nest colonies occurred close to roads, buildings, and
overhead power cables.
Usually, females of Ploceus spp. do not participate in nest construction
activities (Crook 1963; Quader 2006). Ambedkar (1972)
reported that the male Streaked Weaver alone build nests in the Kumaon Terai. But Prakash et al.
(2020) later observed that females also participated in the nest constructions
in Wazirabad. Similarly, I have also recorded that after pairing, females were
also involved in nest construction.
The majority of the nests of Baya Weavers are usually oriented towards the east
direction (Ambedkar 1964; Davis 1971; Quader 2006).
About 87% of nests in Chorao Island in Goa (Borges et
al. 2002) and 88% of nests in Vellore district, Tamil Nadu were oriented
towards the east (Pandian 2021). The present study revealed that 59% of the
nests of Streaked Weaver also face toward the east as in the case of Baya Weavers. The probable reasons for birds constructing
many nests with entrance tubes orienting towards the east would be to protect
their nests from south-west monsoon winds.
The mixed communal roosting and
foraging, consisting of different species, serves as a centre
for the exchange of information regarding the location of food sources and
receives warning about the approach of predators (Zahavi
1971; Gadgil 1972; Ward & Zahavi
1973; Gadgil & Ali 1976). In the present study,
flocks containing individuals of Streaked Weaver, Baya
Weaver, Black-breasted Weaver, Tricolored Munia, White-rumped
Munia, and Indian Silverbill moved collectively for
foraging without any interspecific competition over sharing of food.
Abnormal nesting behaviours occur in other species of the genus Ploceus, such as P. philippinus
(Sharma 1995; Pandian 2021), P. benghalensis
(Mishra 2004), P. manyar (Delacour 1947;
Pandian 2022), P. ocularis (Maclean 1985), P.
velatus, and P. cucullatus
(Collias & Collias
1962; Crook 1963). In the present study, only two abnormal complete nests (1+1
type) were recorded. This corroborates the findings of (Delacour 1947), Collias & Collias (1962),
Crook (1963), Maclean (1985), Sharma (1995), Mishra (2004), and Pandian (2021,
2022).
The habits of smudging mud/dung
on the inner walls of helmet stage nests are prevalent among Streaked Weaver, Baya Weaver, and Black-breasted Weaver when the nest
reaches the helmet stage (Crook 1963; Ambedkar 1969; Borkar
& Komarpant 2003). Individuals of male Streaked
Weaver placed mud and cow dung on the inner wall of helmet stage nests
in Wazirabad (Prakash et al. 2020) and cow dung in Viluppuram,
Tamil Nadu (Pandian 2022). Similarly, in the present study, I have recorded the
males smudging cow dung on the inner wall when the nest construction reached
the helmet stage, and before pairing with a female. An abnormal deposition of
dung on the outer wall was also recorded. The exact reasons for plastering of
dung in helmet stage nests require further studies.
Incident of Rufous Treepie
damaging nests of Baya Weaver was recorded in Arakkonam Taluk, Tamil Nadu (Pandian 2021). In reed beds,
many nests are destroyed by grazing cattle and people harvesting reeds (https://weavers.adu.org.za;
Pandian 2022). The harvesting of T. angustifolia vegetation in c. 700
sq. m and the subsequent abandoning of 21 nests at various developmental stages
by birds in the present study sites deprives their potential breeding ground,
corroborating the views of Pandian (2021, 2022). House Crows, Large-billed
Crows, and Shikras are the major nest predators of
Streaked Weaver (Oschadleus 2021; Pandian
2022). In the present survey House Crows, Large-billed Crows, and Rufous
Treepie were observed in the vicinity of nest colonies corroborating the
observations of Oschadleus (2021) and Pandian (2022).
The impact of these avian predators in large geographical areas requires
further studies.
Conclusion
The present study sites
containing c. 4 ha of T.angustifolia reeds harbour 536 individuals of Streaked Weaver and 349
nests in various stages of development. Birds built nests using fibres of T. angustifolia as nest materials and
followed a seemingly strict mixed communal foraging. Females also participated
in nest constructions. The entrance tubes of maximum nests were found oriented
towards the east. Males had the habit of plastering cow dung on the inner, or
both walls, of helmet stage nests. Harvesting of nest-supporting reeds would
cause not only habitat loss to this species but also the abandoning of nests due
to their exposure. Avian predators such as House Crow, Large-billed Crow, and
Rufous Treepie were sighted in the vicinity of nesting colonies. Despite rapid
urbanization, industrialization, population increase, habitat destruction, and
decreasing areas of cultivation of grains, considerable populations of the
Streaked Weaver exist in the agrarian landscape of the three studied
districts. A special management plan could be devised for the area, considering
the anthropogenic and natural stresses that the habitat is currently subjected
to.
Table 1. Details of the number of
birds, nesting habits, various stages of nests, and orientation of nests of
Streaked Weaver during peak breeding period (2nd week of July 2022).
|
Name of village |
GPS coordinates |
Area size (ha) |
Total number of birds |
Total number of nests |
Stages of nests |
Total number of nests studied
for orientation |
Orientation of nests |
|||||||
Wad stage |
Ring stage |
Helmet stage |
Egg-chamber closed stage |
Complete nests |
East |
West |
North |
South |
|||||||
1 |
Minnal |
13.082oN–79.552oE |
0.20 |
48 |
30 |
1 |
0 |
11 |
1 |
17 |
18 |
11 |
2 |
1 |
4 |
2 |
Kodaikal mottur |
13.060oN–79.403oE |
0.28 |
36 |
19 |
2 |
0 |
7 |
0 |
10 |
10 |
8 |
2 |
0 |
0 |
3 |
Anvarthikanpet |
13.044oN–79.568oE |
0.36 |
46 |
25 |
4 |
0 |
5 |
4 |
12 |
16 |
12 |
3 |
1 |
0 |
4 |
Melkalathur |
13.040oN–79.567oE |
0.20 |
30 |
15 |
3 |
0 |
4 |
4 |
4 |
8 |
5 |
0 |
3 |
0 |
5 |
Periyakarumpur |
12.911oN–79.681oE |
0.16 |
8 |
4 |
0 |
0 |
2 |
2 |
0 |
2 |
2 |
0 |
0 |
0 |
6 |
Urani |
12.151oN–79.907oE |
0.12 |
68 |
43 |
4 |
6 |
19 |
6 |
8 |
14 |
1 |
0 |
13 |
0 |
7 |
Kazhuveli |
12.152oN–79.898oE |
0.20 |
26 |
22 |
2 |
4 |
8 |
4 |
4 |
8 |
6 |
2 |
0 |
0 |
8 |
Marakkanam |
12.158oN–79.916oE |
0.80 |
26 |
21 |
4 |
3 |
4 |
3 |
7 |
10 |
4 |
2 |
4 |
0 |
9 |
Nemili |
12.064oN–79.648oE |
0.24 |
49 |
37 |
5 |
0 |
17 |
5 |
10 |
15 |
9 |
2 |
4 |
0 |
10 |
Veedur |
12.069oN–79.586oE |
1.42 |
199 |
133 |
18 |
15 |
46 |
26 |
28 |
54 |
33 |
5 |
13 |
3 |
|
|
Total |
3.98ha |
536 |
349 |
43 |
28 |
123 |
55 |
100 |
155 |
91 |
18 |
39 |
7 |
Table 2. Frequency distribution
of nest colony sizes and number of nests in each range.
|
Nest ranges (number of nests
per colony) |
Number of nest colonies |
Percentage of number of nest
colonies |
Total number of nests
enumerated |
Percentage of number of nests
in each range |
1 |
1–10 |
12 |
50 |
77 |
22.06 |
2 |
11–20 |
5 |
21 |
66 |
18.91 |
3 |
21–30 |
4 |
17 |
89 |
25.5 |
4 |
31–40 |
1 |
4 |
33 |
9.46 |
5 |
41–50 |
2 |
8 |
84 |
24.07 |
Total |
24 |
100 |
349 |
100 |
Table 3. Details of predators
observed near nest colonies of Streaked Weaver.
|
Name of predator |
Binomials |
No. of sightings |
1 |
House Crow |
Corvus splendens |
34 |
2 |
Large-billed Crow |
Corvus macrorhynchos |
16 |
3 |
Rufous Treepie |
Dendrocitta vagabunda |
09 |
|
Total |
|
59 |
For
figures & images - - click here for full PDF
REFERENCES
Ali, A.M.S., S. Asokan, R. Manikannan & P. Radhakrishnan (2011). Checklist and nesting patterns of
avifauna in and around Mayiladuthurai region, Tamil Nadu, India. Journal of
Threatened Taxa 3(6): 1842–1850. https://doi.org/10.11609/JoTT.o2299.1842-50
Ali, S. &
S.D. Ripley (1987). Compact handbook of the birds of India and Pakistan together with
those of Bangladesh, Nepal, Bhutan and Sri Lanka. 2nd
ed. Oxford University Press, Delhi, i–xlii, 1 l.,
1–737 pp.
Ambedkar,
V.C. (1964). Some Indian
Weaver bird: a contribution to their breeding biology. University of Bombay,
Bombay, 75 pp.
Ambedkar,
V.C. (1969). Observations
on the breeding biology of Finn’s Baya (Ploceus megarhynchus
Hume) in the Kumaon Terai. Journal
of the Bombay Natural History Society 65(3): 596–607 (1968).
Ambedkar,
V.C. (1972). On the
breeding biology of the Blackthroated [Ploceus benghalensis
(Linnaeus)] and the Streaked [Ploceus manyar flaviceps (Lesson)]
Weaver Birds in the Kumaon Terai.
Journal of the Bombay Natural History Society 69(2): 268–282.
Bibby, C.J., N.D. Burgess, D.A.
Hill & S.M. Mustoe (2000). Bird census techniques. 2nd
edition. Academic Press, London, UK, 614 pp.
Borges, S.D., M.
Desai & A.B. Shanbhang
(2002). Selection of nest
platforms and the differential use
of nest building
fibres by the Baya Weaver Ploceus philippinus
Linnaeus 1766. Tropical
Zoology 15: 17—25.
Borkar, M.R. & N. Komarpant
(2003). Observations on the nesting
ecology of Baya Weaver Bird (Ploceus
philippinus, Linn.) in South Goa, with notes on
aberrant nest designs. Ecology, Environment and Conservation 9(2):
217–227.
Clements,
J.F., T.S. Schulenberg, M.J. Iliff, D. Roberson, T.A.
Fredericks, B.L. Sullivan & C.V.
Wood (2022). The eBird/Clements checklist of birds of the World. http://www.birds.cornel.edu/clementschecklist/download.
Accessed on 20 January 2023.
Collias, N.E. & E.C. Collias (1962). An experiment study of the
mechanism of nest building in a weaver bird. The Auk 79: 568–595.
Collias, N.E. & E.C. Collias (1964). The evolution of nest-building
in the weaverbirds (Ploceidae). University of
California Publications in Zoology No. 73.
Crook, J.H.
(1963). A
comparative analysis of nest structure in the weaver birds (Ploceidae).
Ibis 105(2): 238–262.
Davis, T.A.
(1971). Variation in
nest structure of the common weaver bird Ploceus
philippinus of Indaia, Forma
et functio 4: 225─239.
Delacour, J. (1947). Birds of Malaysia. The
Macmillan Company, New York, 382 pp.
De Silva, I.N., A.T. Petorson, J.M. Bates, S.W. Fernando & M.G. Girard
(2017). Phylogenetic
relationships of weaver birds (Aves: Ploceidae): a
first robust phylogeny based on mitochondrial and nuclear markers. Molecular
Phylogenetics and Evolution 109: 21–32.
Dhindsa, M.S. (1982). Ecological studies on the weaver
birds of the Punjab and their control. Dissertation Abstracts 42(7):
2677.
Dhindsa, M.S. & H.S. Toor (1981). Studies on the roosting habits of three species of
weaverbirds in the Punjab. Indian Journal of Ecology 8(2): 156–162.
Dickinson,
E.C. & L. Christidis (eds.) (2014). The Howard and Moore complete
checklist of the birds of the world: 2. Passerines. 4th ed. Eastbourne, UK: Aves Press. Vol. 2 of 2 vols.: Pp. i–lii, 1–752.
Gadgil, M. (1972). The function of communal roosts:
Relevance of mixed roosts. Ibis 114(4): 531–533.
Gadgil, M. & S. Ali (1976). Communal roosting habits of
Indian birds. Journal of the Bombay Natural History Society 72(3):
716–727.
Hussain,
K.J., T. Ramesh, K.K. Satpathy & M. Selvanayagam (2011). A checklist of birds of
Department of Atomic Energy campus, Kalpakkam, Tamil
Nadu. Zoo’s Print 26(7): 13–20.
Maclean, G.L.
(1985). Roberts’
birds of Southern Africa. John Voelter Bird
Book Fund, Cape Town.
Mishra, N.
(2004). Abnormal
nest of the Black-breasted Weaver Ploceus benghalensis. Newsletter for Ornithologists 1(3):
45.
Nagarajan,
V.M. (2021). A checklist
of birds sighted from Sri Sivasubramanium Nadar (SSN)
College of Engineering, Chengalpet, Tamil Nadu.
Bird-o-soar #68. Zoo’s Print 36(1): 19–28.
Oschadleus, H.D. (2021). Weaver watch. https://www.weavers.adu.org.za/.
Accessed on 04 June 2022.
Pandian, M.
(2021). Nesting
habits of Baya Weaver Ploceus
philippinus (Linnaeus, 1776) in rural Arakkonam Taluk, Vellore District, Tamil Nadu, India. Journal
of the Bombay Natural History Society 118: 3–17. https://10.17087/jbnhs/2021/v118/144638.
Pandian, M.
(2022). Nesting and
roosting habits of Streaked Weaver Ploceus manyar in the Veedur wetlands
of Viluppuram district, Tamil Nadu. Indian BIRDS
17(6): 165─173.
Panwar, R.,
S. Panwar, D. Rastogi & A. Rastogi (2020). Finn’s Weaver Ploceus megarhynchus
breeding on Ipomoea reeds, Kumaon,
Uttarakhand. Indian BIRDS 16(5): 152–155.
Prakash, D.,
S.L. Niangthianhoi, R. Kumar & F.A. Khudsar (2020). Nest construction process in
Streaked Weaver Ploceus manyar
Indian BIRDS 15(6): 168–174.
Quader, S. (2006). What makes a good nest? Benefits
of nest choice to female Baya Weavers (Ploceus philippinus).
The Auk 123(2): 475–486 (with three tables and three text–figs.).
Raj, P.P.N.,
J. Ranjini, R. Dhanya, J.
Subramanian, P.A. Azeez & S. Bhupathy (2010). Consolidated checklist of birds
in the Pallikaranai wetlands, Chennai, India. Journal
of Threatened Taxa 2(8): 1114–1118. https://doi.org/10.11609/JoTT.o2220.1114-8
Rasmussen,
P.C. & J.C. Anderton (2005). Birds of South Asia: The Ripley Guide. 1st
edition. Smithsonian Institution and Lynx Edicions,
Washington, D.C. and Barcelona, 2 vols. 1–378 pp.; 1–683 pp.
Sharma, S.K.
(1995). A study of
abnormal nests of Baya Weaver Bird Ploceus philippinus (Linn.) in
Rajasthan. Journal of the Bombay Natural History Society 92(1): 67–76.
Sharma, S.K.
(1997). Causes of
destruction of nests of Weaver Birds in Rajasthan. Journal of the Bombay Natural
History Society 94(3): 515–520.
Siva, T. & P. Neelanarayanan (2017). Checklist of birds of Koothapar Big Tank in Tiruchirappalli District, Tamil Nadu.
ENVIS Newsletter Sarovar Saurabh 13(3): 1–6.
Srinivasulu, C., V.V. Rao & V. Nagulu (2000). Nesting of Ploceus
philippinus (Linn.) and Ploceus
manyar (Horsfield) on
mangrove and associated species in Coringa Wildlife
Sanctuary, Andhra Pradesh. Journal of the Bombay Natural History Society 97(3):
432.
Vasanth, M.
(1990). Birds of
Dharmapuri District, Tamil Nadu, India. Records of the Zoological Survey of
India 86(2): 289–314.
Ward, P.
& A. Zahavi (1973). The importance of certain
assemblages of birds as “information for food finding”. Ibis 115(4):
517–534.
Zahavi, A. (1971). The function of pre-roost gatherings
and communal roosts. Ibis 113(1): 106–109.