Trichoglossus haematodus
SUBFAMILY
Psittacinae
TAXONOMY
Psittacus haematod (sic.) Linnaeus, 1771, Ambon. Twenty-two
subspecies.
OTHER COMMON NAMES
English: Rainbow lory, coconut lory; French: Loriquet а tкte
bleue; German: Allfarblori; Spanish: Lori Arcoiris.
PHYSICAL CHARACTERISTICS
10 in (26 cm); 3.5–5.8 oz (100–167 g). Brightly colored bird
with red, yellow, and green plumage; long, tapering tail. Polytypic
species with geographical variation in colors of head and
breast.
DISTRIBUTION
T. h. haematodus: south Moluccas, west Papuan Islands, and
northwest New Guinea, Indonesia. T. h. mitchelli: Bali and
Lombok, Indonesia. T. h. foresteni: Sumbawa, Indonesia. T. h.
djampeanus: Tanahjampea, Indonesia. T. h. stresemanni: Kalaotoa,
Indonesia. T. h. fortis: Sumba, Indonesia. T. h. weberi: Flores,
Indonesia. T. h. capistratus: Timor. T. h. flavotectus: Wetar
and Romang, Indonesia. T. h. rosenbergii: Biak Island, Irian
Jaya, Indonesia. T. h. intermedius: north New Guinea. T. h.
imicropteryx: east New Guinea. T. h. caeruleiceps: south New
Guinea. T. h. nigrogularis: Aru and east Kai Islands, Indonesia.
T. h. brooki: Spirit Island, in Aru Islands, Indonesia. T. h.
massena: Karkar Island, Bismarck Archipelago, Solomon Islands,
and Vanuatu. T. h. flavicans: New Hanover and Admiralty
Islands, Papua New Guinea. T. h. nesophilus: Ninigo and
Hermit Islands, Papua New Guinea. T. h. deplanchii: New
Caledonia and Loyalty Islands. T. h. septentrionalis: Cape York
Peninsula, north Australia. T. h. moluccanus: east Australia; introduced
to southwest Australia. T. h. rubritorquis: north Australia.
HABITAT
Lowlands to mid-montane elevations. Wide variety of wooded
habitats wherever flowering plants are available, ranging from
mangroves and coastal heathlands to savanna woodland, gallery
forest, secondary growth, and rainforest; colonizes man-made
habitats, especially coconut plantations, orchards, and suburban
gardens; prefers edges or clearings rather than interior of
closed rainforest; tolerates depauperate scrubland or plantations
on quite small atolls.
BEHAVIOR
Resident, though pronounced local movements in response to
flowering of food plants causes marked fluctuations in numbers.
In pairs or flocks of few birds to hundreds depending on
food availability; noisy and active, constantly flying back and
forth through or above canopy and clambering amidst foliage
to get at flowers or fruits; screeching call-notes always betray
presence; often in company of other fruit-eating birds; becomes
tame in household gardens or at feeders; very swift, direct
flight.
FEEDING ECOLOGY AND DIET
Compressed, pointed bill and “brush-tipped” tongue used to
extract pollen and nectar from flowers; also fruits, berries,
seeds, leaf buds, and insect larvae; in Australia, feeds principally
on Eucalyptus and Banksia flowers; fond of cultivated fruits and
unripe “milky” grain; readily comes to garden feeders to take
fruit, seed, or artificial nectar mixes.
REPRODUCTIVE BIOLOGY
Monogamous, paired birds staying together and readily discernible
within flocks. Breeding season variable in different
parts of range, but nesting recorded most months. Courtship
display features wing-fluttering to show colorful underwings,
side-to-side swaying with neck arched forward and eye pupils
dilated; nest in tree-hollow; at times two or more nests in same
tree, but hollow entrances defended; nesting on ground
recorded from Admiralty Islands, Papua New Guinea; clutch of
two to three eggs incubated by female for about 25 days;
young birds fledge at about eight weeks.
CONSERVATION STATUS
Generally common, locally plentiful; in some districts most
common parrot; in Australia, benefits from cultivation of native
flowering plants in gardens, and numbers increasing. Listed on
CITES Appendix II.
SIGNIFICANCE TO HUMANS
In Australia, popular visitor to garden feeders, and major attraction
at tourist parks where hundreds come to feed from
trays held by visitors. In some regions hunted for food and
feathers, latter used in ceremonial headdresses.
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