Mérion couronné

Malurus coronatus

Petit oiseau avec une longue queue bleue relevée. Le mâle nicheur a une calotte violette brillante avec un trait loral et un collier noirs. La femelle a des taches jugales rouille foncé proéminentes. Le mâle non nicheur a des taches jugales noires proéminentes. Cette espèce préfère les habitats riverains, en particulier lorsqu'ils incluent des Pandanus (palmier-vis) et une longue végétation herbeuse.

Identification

The purple-crowned fairywren is a small, sexually dimorphic, bird measuring approximately 14 cm (5.5 in) in length, with a wing-span of approximately 16 cm (6.3 in) and weighing only 9–13 g (0.32–0.46 oz). It can be differentiated from other North Australian fairywrens by the presence of cheeks patches and the deep blue color of their tails. The plumage is brown overall, with the wings more greyish brown and the belly cream-buff. The blue tail is long and upright, and all except the central pair of feathers are broadly tipped with white. Their bill is black and the legs and feet are brownish grey. Although there is a slight geographical variation between the two subspecies, only the difference in colour of mantle is noticeable in the field. The crown and nape of M. c. macgillivrayi is slightly bluer, and its mantle and upper back has weak blue-grey shading, whereas the slightly larger M. c. coronatus has a browner back, as well as a buff-coloured, rather than white, breast and belly.<p>During the breeding season, adult males develop the spectacular bright purple feathers on their crown. This is bordered by a black face mask and capped with an oblong black spot on top of the head. During the non-breeding season, the male's colourful crown is replaced by grey/brown feathers and its black mask with black cheek patches and an off-white to pale grey orbital ring. The adult female differs in having a blue-tinged grey crown, chestnut ear-coverts, and a greenish blue tail. Immature birds are very similar to adult females except for a duller coloration, a brown crown, and longer tail, though male birds start to show black feathers on the face by six to nine months <p>Within a group, males who are breeding molt into their bright crown earlier than their non-breeding subordinates, and do so even sooner after heavy rains the preceding season. Experiments have demonstrated that breeding males view more colourful plumage among nearby males as a source of competition, and behave more aggressively towards them.<p>The song of the purple-crowned fairywren is distinct from that of other fairywrens – it is of lower pitch, and quite loud. Breeding pairs use song to communicate and use duets to ward off itinerant fairywrens from their territory. Three calls have been recorded: a loud reel cheepa-cheepa-cheepa, a quieter chet – a contact call between birds in a group when foraging, and an alarm call – a harsh zit.

Taxonomie

The purple-crowned fairywren was first collected in 1855 and 1856 by the explorer Joseph Ravenscroft Elsey at Victoria River and Robinson River. The species was first described by the ornithologist John Gould in 1858. The specific name comes from the Latin word cǒrōna, meaning crown. Gregory Mathews described the subspecies M. c. macgillivrayi in 1913. Subspecies designation was originally based on differences in plumage coloration and body size of museum skins. More recent genetic analyses continue to support this split. The species has also been placed in the monotypic genus Rosina, but protein evidence supports its placement in the current genus. Alternative names for the purple-crowned fairywren include crowned superb warbler, lilac-crowned fairywren, lilac-crowned wren, mauve-crowned wren, purple-crowned warbler, purple-crowned wren, and purple-crowned wren-warbler.<p>It is one of 11 species in the genus Malurus, commonly known as fairywrens. Within the genus it is most closely related to the splendid fairywren and superb fairywren. It is also sometimes placed as a sister to clade including the two "blue wrens" along with the white-shouldered fairywren, white-winged fairywren, and the red-backed fairywren, also called the bicoloured wrens.<p>Like other fairywrens, the purple-crowned fairywren is unrelated to the true wrens. It was previously classified as a member of the Old World flycatcher family Muscicapidae and later as a member of the warbler family Sylviidae before being placed in the newly recognised Maluridae in 1975. More recently, DNA analysis has shown the family Maluridae to be related to the Meliphagidae (honeyeaters), and the Pardalotidae in the large superfamily Meliphagoidea.<p>Combined mitochondrial and nuclear DNA from the purple-crowned fairywren genome suggest that its lineage diverged from those of the splendid and superb fairywrens c. 7–8 million years ago. More recently, the purple-crowned fairywren appears to have diverged from a group that now includes the blue-breasted fairywren, the red-winged fairywren, the lovely fairywren, and the variegated fairywren around six million years ago.<p>These evolutionary radiations followed an earlier split of the grasswrens Amytornithinae from what would become the emu-wrens and fairy wrens approximately 23 million years ago.<p>Two subspecies are currently recognized:

Nom scientifique
Malurus coronatus
Autorité
Gould, 1858
Ordre
Passériformes
Famille
Maluridés
Genre
Malurus

Répartition et habitat

The species occurs across the wet-dry tropics of northern Australia, and is found in the Kimberley region of Western Australia, in the Victoria River region of the Northern Territory, and in the south-western sub-coastal region of the Gulf of Carpentaria in Queensland. Whilst the species’ distribution spans more than 1,500 km (930 mi), it is constrained by the quality and extent of riparian vegetation along waterways. A natural geographic barrier of approximately 300 km (190 mi) of unsuitable habitat separates the two subspecies. The western subspecies M. c. coronatus occurs in the midsections of large river catchments that drain the Central Kimberley Plateau, and along sections of the Victoria River. The eastern subspecies M. c. macgillivrayi occurs along most rivers draining into south-western and southern Gulf of Carpentaria from Roper River in Northern Territory to Leichhardt and Flinders Rivers in Queensland.<p>The purple-crowned fairywren is a riparian habitat specialist that occurs in patches of dense river-fringing vegetation in northern Australia. Its preferred habitat, which lines the permanent freshwater creeks and rivers, consists of a well-developed mid-storey that is composed of dense shrubs (i.e. Pandanus aquaticus and/or a freshwater mangrove, Barringtonia acutangula), as seen in the Kimberley region or areas of 1.5–2 m (4 ft 11 in – 6 ft 7 in) tall, dense thickets of river grass dominated by Chionachne cyanthopoda as seen in the Victoria River District. A tall dense canopy of emergent trees, used as a temporary refuge during flooding events that submerge the mid-storey, is often dominated by Eucalyptus camaldulensis, Melaleuca leucadendra, Melaleuca argentea and Ficus spp.

Migration
Resident species

Comportement

Like all other species in the genus Malurus, the purple-crowned fairywren is a cooperative breeder and lives in sedentary groups that maintain their territories, often arranged linearly along creeks and rivers, year-round. However, unlike other species in the genus that are highly promiscuous, purple-crowned fairywrens display high levels of fidelity and low rates of extra-pair paternity. Groups generally consist of a breeding pair that is helped by one to six offspring from previous broods, and helpers may stay with their parents for several years before attempting to breed. Only the dominant pair in a group reproduces, and individuals can remain un-reproductive subordinates for several years. These subordinates help raise the offspring, improving productivity as well as the survival of the breeding pair.<p>Group territories are maintained throughout the year, and usually the same site (or area) is used year after year. The spatial arrangement of purple-crowned fairywren territories differ depending on what plant species dominate the understory. Territories in Pandanus are usually arranged in a linear fashion, and generally occupy between 50–300 m (160–980 ft) of river length, whereas territories may be arranged in a mosaic pattern in areas where the understory consists of tall river-grasses such as C. cyanthopoda.<p>Breeding can occur at any time throughout the year, if conditions are suitable, with peaks in the early (March to May) and late (August to November) dry season. Most nests have been recorded close to the ground in thickets of river grass, C. cyanthopoda and P. aquaticus. Only the females build the small dome shaped nests constructed mainly of fine rootlets, grass, leaves and strips of bark. Pairs may produce up to three broods per year. A clutch containing 2–3 eggs is laid over successive days, and is incubated by only females for 14 days, and chicks fledge after ten days. Fledglings are unable to fly and stay in dense cover for a week and are fed by members of the family group for at least another three weeks.<p>Incestuous matings by the purple-crowned fairywren result in severe fitness costs due to inbreeding depression (greater than 30% reduction in hatchability of eggs). Females paired with related males may undertake extra pair matings that can reduce the negative effects of inbreeding (although social monogamy occurs in about 90% of avian species, an estimated 90% of socially monogamous species exhibit individual promiscuity in the form of extra-pair copulations, i.e. copulation outside the pair bond). Although there are ecological and demographic constraints on extra pair matings, 43% of broods produced by incestuously paired females contained extra pair young. In general, inbreeding is avoided because it leads to a reduction in progeny fitness (inbreeding depression) largely due to the homozygous expression of deleterious recessive alleles.<p>The population genetic structure of the species suggests it generally disperses along waterways. The average natal dispersal of the purple-crowned fairywren is less than 3 km (1.9 mi) of river distance in quality habitat, but movements of up to 70 km (43 mi) of river distance have been recorded. Most dispersal occurs when helpers abandon their natal territories in search of their own breeding territory. Dispersal is sex-biased with most subordinate males remaining in their natal territory or moving to neighbouring territories, while females generally disperse further. Females are capable of both long-distance and between-catchment dispersal.<p>The species is mainly insectivorous. Birds consume a range of small invertebrates such as beetles, ants, bugs, wasps, grasshoppers, moths, larvae, spiders, and worms and small quantities of seeds. They forage for their prey amongst foliage and in the leaf litter on the ground that may have accumulated as debris during floods. Group members will forage separately, hopping rapidly through the dense undergrowth, but remain in contact with each other by making soft chet sounding calls.

Conservation

Tendance de la population
declining

Photos

Distribution

Chants d'Oiseaux

Autres Oiseaux

Ermite à menton noir

Ermite à menton noir

Phaethornis augusti

Un grand colibri brunâtre à longue queue. Gris pâle en dessous avec de fortes marques faciales et un croupion roux contrastant ; les larges pointes blanches des plumes de la queue sont un signe distinctif clé. On le trouve dans les forêts sèches et le long des lisières de savane, où il visite des sources de nectar très espacées et est souvent vu se déplaçant rapidement entre elles. Remarquablement curieux, il s'arrête souvent pour évaluer une personne avant de repartir rapidement ; la quantité de blanc dans la queue est particulièrement évidente lorsque l'oiseau s'envole. Les mâles chantent depuis des perchoirs bas ; le chant consiste en deux notes grinçantes suivies de trois notes plus rapides et plus aiguës, données en alternance, encore et encore. Le cri de vol est un fort couinement, similaire à celui d'autres grands ermites. Se distingue le mieux des ermites à longue queue et à grand bec par sa coloration plus pâle et grisâtre et le blanc étendu dans la queue.

Gros-bec ponceau

Gros-bec ponceau

Pyrenestes sanguineus

Un pinson brun à bec trapu avec un croupion rouge électrique, une queue rouge et un capuchon rouge qui s'étend de la gorge à la nuque ; le capuchon du mâle est plus grand que celui de la femelle et s'étend le long des flancs. Le juvénile est plus terne que l'adulte. Un résident secret et peu commun, restreint à la Haute Guinée, trouvé en couples dans les forêts marécageuses, les broussailles près des ruisseaux et les fourrés près de l'eau dans les forêts primaires et secondaires ; parfois aussi dans les cultures. Son chant est une série variable de bourdonnements et de sifflements, et son cri est un "tsut…tsut" strident. Le Casse-graines à ventre noir mâle diffère du Cramoisi par un dos et un ventre noirs (non bruns) ; les femelles et les juvéniles sont presque identiques mais ne se chevauchent que dans l'est de la Côte d'Ivoire.

Oropendola verte

Oropendola verte

Psarocolius viridis

Un grand oiseau trapu. Son plumage vert et châtain peut sembler principalement noir dans certaines conditions et à distance. Notez sa taille, sa queue jaune et ses battements d'ailes profonds et ramés. Il se distingue de manière fiable des autres oropendoles à plumage vert par son bec vert pâle et rouge. Trouvé dans la canopée et les lisières de la forêt tropicale humide, ainsi que le long des rivières, dans les villages et dans les savanes boisées. Les groupes se déplacent bruyamment à travers la canopée de la forêt à la recherche de fruits et de fleurs. De grandes volées sont parfois observées se déplaçant entre les zones de repos et d'alimentation. Le chant distinctif du mâle peut être entendu à grande distance.

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