Nesting behaviour of the Baya Weaver
bird, Ploceus philippinus(Ploceidae) and the life-cycle of the Plains Cupid
butterfly, Chilades pandava(Lycaenidae) with the red-listed Cycas sphaerica and C. beddomei(Cycadaceae)
A.J. Solomon Raju
Department of Environmental Sciences, Andhra University,
Visakhapatnam, Andhra Pradesh 530003, India
Email:ajsraju@yahoo.com
Date of publication (online): 26
August 2009
Date of publication (print): 26
August 2009
ISSN 0974-7907 (online) |
0974-7893 (print)
Editor: Cleo Cervanicia
Manuscript details:
Ms # o2173
Received 13 February 2007
Final received 25 July 2009
Finally accepted 28 July 2009
Citation: Raju, A.J.S. (2009). Nesting behaviour of the Baya Weaver
bird, Ploceus philippinus(Ploceidae) and the life-cycle of the Plains Cupid
butterfly, Chilades pandava(Lycaenidae) with the red-listed Cycas sphaerica and C. beddomei(Cycadaceae). Journal of Threatened Taxa 1(8): 429-433.
Copyright: © A.J. Solomon Raju 2009. Creative Commons Attribution 3.0 Unported License. JoTT allows
unrestricted use of this article in any medium for non-profit purposes,
reproduction and distribution by providing adequate credit to the authors and
the source of publication.
Author Details: Dr. A.J. Solomon Raju is currently
working as Associate Professor. He is
presently working on endemic and endangered plant species in southern Eastern
Ghats forests with financial support from DST, CSIR and UGC.
Acknowledgement: The work is an
outcome of a research project funded by the Council of Scientific and
Industrial Research, New Delhi.
Abstract:The Baya Weaver bird, Ploceus philippinus utilizes the well developed leaves ofCycas sphaericafor nest construction and offspring production. It constructs nest on the leaf
tips of this species; the nest material used is exclusively Dendrocalamus strictus. This bird species does not utilize Cycas beddomei for nest construction and offspring
production. The Plains Cupid butterfly, Chilades pandavautilizes the newly emerging leaves of both C. sphaericaand C. beddomei for raising its
offspring. In both the Cycas species, the new leaves emerge as a crown at
the top of the plant; the larvae of C. pandava feed
on these leaves and make the plant as leafless until the next leaf flushing
season. New leaf production occurs after
coning event in Cycas species; coning is not
annual event. In consequence, the plants
utilized by C. pandava for the production of
its offspring remain leafless until the next coning season and their survival
during this period depends on the nutrient status within the shoot system and
in the soil system. The study suggests
that there is no direct or indirect interaction between C. pandava and P. philippinus. C. sphaericaserves as a host plant for these two animal species at different times; but the
interaction of these animal species is dependent on the leaves only; C. pandava on newly emerging leaves while P. philippinus on well developed leaves.
Keywords:Animal plant interaction, Chilades pandava, Cycas beddomei, Cycas sphaerica, Dendrocalamus strictus, Ploceus philippinus
Introduction
Cycas sphaerica Roxb. (Cycadaceae) occurs in dry forests and woodlands in the
Eastern peninsular region of India on hills distributed from Chennai north to Bhubaneshwar; a population of more than 500 trees exists atJalantrakota in the low elevation dry deciduous
forest in Srikakulam District of Andhra Pradesh. This species falls under the Data Deficient
category and is included in CITES Appendix II that allows trade in
wild-cultivated seeds or plants as long as there is no detrimental impact on
the survival of wild populations. C. beddomei Dyer is included in the IUCN Red list and is a
Critically Endangered species restricted to the SeshachalamHills of the Eastern Ghats in Andhra Pradesh (Hill et al. 2003; Reddy et al.
2006). There is no information on any
aspect of C. sphaerica, and little information
available on C. beddomei.
The BayaWeaver Bird, Ploceus philippinusis widespread and common within its distribution area but is prone to local,
seasonal movement in search of nesting sites and food (BirdLifeInternational 2008). It breeds during
the monsoon period (Rasmussen & Anderton2005). The occurrence and breeding of
this bird in its distribution range are therefore related to the availability
of nest sites and food resources. In
this paper, the association and nesting behaviour of P.philippinus, and the association of life cycle of
the Plains Cupid butterfly, Chilades pandava with C. sphaericaat Jalantrakota Reserve Forest and also with C. beddomei at Tirumala Hills is
described based on field studies conducted at their natural sites. In C. sphaerica-P. philippinus association, it is found that the
former is neither benefited nor harmed while the latter is benefited by using
it as a nest host. In Cycas species-C. pandava association, the
former are harmed by defoliation while the latter is benefited by using it as a
host for raising its offspring.
Materials and Methods
Cycas sphaerica occurring at JalantrakotaReserve Forest and C. beddomei at Tirumala Hills were used for the present study. The study was conducted during
2007-2008. The morphological
characteristics were examined in the field. The sexual status of the plants was recorded when the plants
flowered. The association of the Baya Weaverbird, Ploceus philippinus with C. sphaericawas carefully examined in the field. The
nest materials used by the bird were recorded visually and also by using
binoculars. The nest construction
activity of the bird on the plant was observed by standing at the close
quarters and by using binoculars; the entire length of the day was spent at the
site for collecting accurate information. Seven days were used for this purpose. The nest structure was also examined and the details are noted. The association of the Plains Cupid butterfly,Chilades pandavawith the newly emerging leaves of both the species of Cycas was examined in detail. The entire
life cycle of the butterfly was observed during the study period.
Observation
Plant
characteristics of Cycas species:
C. sphaerica is a
medium-sized palm-like shrub with an erect solitary stem up to 2.36±1.4 m long
(Range 1-5m) and 12-30 cm diameter. Stem
base is not strongly swollen and bark is thick with persistent leaf bases. The apex of the stem is crowned with 30-40
leaves; each leaf is 95-185 cm long. C.beddomei is a small palm-like shrub with an erect
solitary stem up to 1.23±0.18 m long (Range 1-1.6m), often shorter, 15-20 cm
diameter. The apex of the stem is
crowned with 20-30 leaves; each leaf is 90.95±16.91 cm long (Range 75-135
cm). Both C. sphaericaand C. beddomei are dioeciousand the sex of each individual is identifiable only when male or female cones
are formed.
Association
of Ploceus philippinuswith C. sphaerica:
Cycas sphaerica and Dendrocalamus strictus (Roxb.) Nees (Bambusaceae) are the most
prominent species in the Jalantrakota Reserve
Forest. The BayaWeaverbird, Ploceus philippinusL. constructs new nests on the leaf tips of C. sphaerica. Breeding males with a bright yellow crown,
blackish-brown bill, upper parts dark brown streaked with yellow, with a yellow
breast and cream buff below look different from breeding females. The male constructs the entire nest while
female gives finishing touches to the nest if accepted by her (Borges et al.
2002). Both the sexes of the bird were
found on C. sphaerica during nest construction
phase (Image 1a,b). The males used their strong stout beaks to torn strips of 20-35 cm
length from the culms of D. strictus (Image
1c); each strip was transported with the beak to the nest platform to weave and
knot them while building their nests. They used only fresh, green strips of culms and grass blades to
construct the nests. D. strictus being a bamboo, its fiber possesses excellent
strength properties, especially tensile strength, which is required to
withstand wear and tear of the extensively used components of the nest. Further, it is also known to possess silica
particles in the epidermis layer of culm; these
particles as very fine spicules give a definite
interlocking between the interwoven fibers, thereby giving necessary stability
to the stalk (Kumar et al. 1994; Borges et al. 2002). It is reported that the plant fibers free of silicious deposits are preferred for construction of the
egg chamber to avoid discomfort to the altricalhatchlings (Borges et al. 2002). But,
the weaver bird has been found to use almost exclusively D. strictus fiber for the construction of the entire nest,
which may be due to non-availability of other materials in the area.
The Weaverbird’s nest is unique for
delicate craftsmanship of building intricate pendant nests. It has been reported that the bird uses Cocos nucifera,
Eucalyptus sp., Careya arborea, Saccharum sp. and Bambusa sp. as nest building platforms (Borges et
al. 2002). The criteria for the
selection of such plants by the bird could be that their tall sturdy unbranched trunks and their crown of swaying fronds provide
protection against intruders, lashing rains and violent winds, and provide a
wider display surface for males to draw the attention of prospective female
mates and withstand climatic vagaries (Davis 1974). But, the present study indicates that the
bird uses C. sphaerica trees which are more
than 3 m tall with a crown of leaves. This Cycas species provides the necessary
protection as mentioned above for the nests of the weaver bird.
The nests observed are pendulous,
hanging from the leaf tips; they are mono-storied, stalked, retort shaped, with
a central nesting chamber and a long vertical tube that leads to a side entrance
to the chamber (Venkataramani 1981). Sharma (1995) reported that this weaver bird
rarely constructs stalk-less nests because such nests are hardly ever accepted
by female birds. There are five stages
in the construction of a nest: initial attachment, roof and egg/brood chamber, ante-chamber, entrance and entrance tube. The last stage is taken up by the male bird
after the eggs have been laid by female bird. Two eggs per nest were observed; they are hard, pure white and stout in
structure (Venkataramani 1981; Sharma 1995) (Image
1d-g). There were some partially
completed nests without any eggs on each tree that was used by the bird for
nesting; these appear to be a result of non-acceptance of such nests by female bird
(Image 2).
Wood (1926) mentioned that weaver birds,
instead of building a nest once or twice a year, may repair old ones. At the study site, the males constructed all
new nests. This is because leaf fall in C.sphaerica is an annual event and nests of the
weaver bird fall to the ground along with the leaves. C. sphaericabeing an ancient woody perennial seed plant, it is the sole plant that is
available as nest building platform for P. philippinusin the Jalantrakota Reserve Forest. In C. sphaerica-P. philippinus association, the plant is not harmed
or benefited while the bird is benefited by using the leaf tips of the plant as
nest site. C. beddomeiis not suitable as a nest host plant for the weaver bird, for the reasons that
the plant height is less and its leaves are situated near to the ground
level.
Association
of Chilades pandavawith C. sphaerica and C. beddomei:
C. pandava utilizes C. sphaerica and C. beddomeifor oviposition during summer season. In both the Cycasspecies, the new leaves emerge from the apex of the stem immediately after
coning in both male and female trees. New leaf production is absent in trees that have not produced cones and
such trees bear dry old leaves or remain leafless. The coning event and the number of coned
trees in the population seem to indicate the prevalence of pest - C. pandava. It oviposits on the very young leaves which are still in
curled up stage on coned trees (Image 3e,f). Eggs are very small, pale green colour (Image 3a), laid singly on newly emerging circinately coiled leaves before they are open and also on
the tender leaves emerging from seedlings (Image 3g). Early instar larvae
are purple (Image 3b) while later larval instars are green. Pupa is grey colouredand human foot-shaped (Image 3c,d). The caterpillars feed only on new leaves
before they harden but leave the rachis intact (Image 3h). In case of seedlings, the caterpillars feed
on leaves and also bore young stem causing death of the seedlings. Damaged
trees show wilting of leaf rachis without reemergence of new leaves in the same
year and their survival depends on the nutrient environment within them and in
the forest floor. Repeated defoliation
on the same trees in successive years may lead to their mortality. A good population of this butterfly
caterpillar could result in the complete defoliation of new leaves. Adults emerge within three weeks but they are
not associated with Cycas trees for
food purpose.
All cycads produce certain allelochemicals which are costly and risky for them but
serve a protective function in evolution (Fraenkel1959; Wink 1999). Cycasinis an important chemical produced in Cycasspecies; it is toxic to insects but the latter reduce the load by rapid
excretion or detoxification or sequester as an acquired defensive
substance. Cycad beetle, Rhopalotria bite off and eliminate trichomes from the surface of the cycad sporophyllbefore feeding, which may be because of its high toxin content (Norstog et al. 1992). The lycaenid butterfly, Eumaeus atala utilizes Cycads as larval host plant. Eggs are crowned by orange scales, detached
from their mother’s abdomen. These
scales stick by their originally distal tips to the varnish of the egg-shell
and are pulled out of their original sockets during oviposition. It is a case of egg protection by aposematism which is absent in C. pandava(Rothschild 1992). E. atala larvae store the ingested cycasinand transfer it to pupae and adults to avoid bird predators. The adults store 40% of their total cycasin in the wings where the birds try to seize for
food. This is a case of aposematism which by definition is a secondary defense
mechanism that warns potential predators of the existence of another primary
defensive mechanism (Rothschild et al. 1986; Bowers & Larin1989; Bowers & Farley 1990). Cycasin might force predators to combine sensing and
memorizing unpalatability with eyespots (Nash et al.
1992; Ackery et al. 1993). C. pandavawith eyespots on the margins of hind wings too might be using Cycas species as hosts to acquire cycasin to the levels required in adult wings to send
warning signals to its predators so as to protect themselves from
predation. In C. sphaerica, C. beddomei-C. pandava association, the
plants are not benefited but harmed by the butterfly. The butterfly by feeding on the newly
emerging leaves contributes to the failure of sexual reproduction due to
non-availability of photosynthate and also affects
the survival rate of both female and male trees as their natural habitat is
rocky and characterized by nutrient-deficient soil environment. C. pandavais benefited by utilizing the plants for raising the offspring from egg to
adult stage and by acquiring cycasin chemical for
protection against its predators.
The study shows that there is no
interaction between C. pandava and P. philippinus; the former utilizes the newly emerging
leaves of C. sphaerica and C. beddomei while the latter utilizes well developed
leaves of C. sphaerica for nest construction
and for raising its offspring. There is
no overlap of interactions of these two animal species with C. sphaerica. The
new leaf production event in both Cycas species
occurs after coning. The eggs of C. pandava hatch and produce Ist instar; subsequent
larval instars emerge due to continuous feeding on the emerging leaves. Then, the larvae pupate and finally adults
emerge. In this process, the entire
crown of newly emerging leaves disappears and the plants become leafless until
the next leaf flushing season. The
plants which were not utilized by butterflies produce a crown of new leaves. P. philippinusutilizes leaf tips from such plants. Therefore, there is no direct or indirect interaction between C. pandava and P. philippinus. C. sphaericaserves as a host plant for these two animal species at different times; but the
interaction of these animal species is dependent on the leaves only; C. pandava on newly emerging leaves while P. philippinus on well developed leaves.
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