Golden-tailed Sapphire Chrysuronia oenone Scientific name definitions
Text last updated January 29, 2016
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Species names in all available languages
Language | Common name |
---|---|
Catalan | colibrí safir cua de foc |
Czech | kolibřík zlatochvostý |
Dutch | Bronsstaartsaffierkolibrie |
English | Golden-tailed Sapphire |
English (United States) | Golden-tailed Sapphire |
French | Colibri oenone |
French (France) | Colibri oenone |
German | Bronzeschwanz-Saphirkolibri |
Japanese | コガネオハチドリ |
Norwegian | gyllenhalekolibri |
Polish | złotogonek |
Portuguese (Brazil) | beija-flor-de-cauda-dourada |
Portuguese (Portugal) | Beija-flor-de-cauda-dourada |
Russian | Бронзовохвостый сапфир |
Serbian | Zlatorepi safir kolibri |
Slovak | kolibrík bronzovochvostý |
Spanish | Zafiro Colidorado |
Spanish (Ecuador) | Zafiro Colidorado |
Spanish (Peru) | Zafiro de Cola Dorada |
Spanish (Spain) | Zafiro colidorado |
Spanish (Venezuela) | Colibrí Cola de Oro |
Swedish | bronsstjärtad smaragd |
Turkish | Altın Kuyruklu Zümrüt |
Ukrainian | Колібрі-сапфір золотохвостий |
Chrysuronia oenone (Lesson, 1832)
Definitions
- CHRYSURONIA
- oenone
The Key to Scientific Names
Legend Overview
Introduction
The golden-rufous tail of the Golden-tailed Sapphire helps indentify both sexes since they tend to appear dark. These sapphires are found around humid forest edges, second growth, light woodlands, plantations, gardens, and partially open areas with scattered trees. During the dry season, individuals congregate at large flowering trees and try to defend small floral territories. In less dry periods, birds often forage singly at flowers at various levels. The early rainy season also coincides with when males sing the most. Large and sudden seasonal migrations of these sapphires have been noted in Venezuela.
Field Identification
9·5–10 cm; male 4·7–6·3 g (1), female 4·3–5·3 g (1). Maxilla black, mandible red with black tip. Male has entire head and throat violet-blue, breast glittering green passing to bronzy green on belly, undertail-coverts bronze edged with whitish; back bright green, shading through bronze-green to brilliant coppery uppertail-coverts and copper-bronze tail . Female has crown blue, shading to green on back and copper-bronze on uppertail-coverts and tail; below mostly whitish, heavily flecked with blue-green on sides of throat and neck, and green on sides and across chest, bronze-green on flanks; undertail-coverts with bronzy centres. Juvenile male has crown dull green, throat dusky grey with dull buffy feather fringes and chest duller green; the first generation of blue feathers on head and throat are more blue, less violet than in adult male; juvenile female has green spotting below duller and more bronzy, less bluish than in adults. In race <em>josephinae</em> , male has throat mostly green, rump green contrasting more with coppery tail-coverts ; alleni has no blue on throat and little or none on malar area, with rump more or less coppery in both sexes.
Systematics History
Editor's Note: This article requires further editing work to merge existing content into the appropriate Subspecies sections. Please bear with us while this update takes place.
Proposed type locality of Trinidad seems unlikely, as there are apparently no definite records with specific localities, and the species has not been mentioned in any work on Trinidad birds since 1900. Race josephinae relatively distinctive, owing to male’s green not blue throat (score 3), and less rich emerald-green mantle to rump (1); but no other characters distinguishing it are known; more study needed. Race alleni and proposed race peruviana may not be adequately separable from josephinae. Several other races proposed: longirostris from E Colombia differs from nominate only in average bill length; azurea, supposedly from W Ecuador but no definite records thence (in fact, probably from E Ecuador), has characters of a subadult male of oenone; and intermedia of upper Amazonia probably of hybrid origin. Described form Thalurania lerchi, known from Bogotá trade skins, is apparently a hybrid between present species and Thalurania furcata. Three subspecies currently recognized.Subspecies
Chrysuronia oenone oenone Scientific name definitions
Distribution
Chrysuronia oenone oenone (Lesson, 1832)
Definitions
- CHRYSURONIA
- oenone
The Key to Scientific Names
Legend Overview
Chrysuronia oenone josephinae Scientific name definitions
Distribution
Chrysuronia oenone josephinae (Bourcier & Mulsant, 1848)
Definitions
- CHRYSURONIA
- oenone
- josephina / josephinae
The Key to Scientific Names
Legend Overview
Chrysuronia oenone alleni Scientific name definitions
Distribution
Chrysuronia oenone alleni (Elliot, 1888)
Definitions
- CHRYSURONIA
- oenone
- alleni
The Key to Scientific Names
Legend Overview
Distribution
Editor's Note: Additional distribution information for this taxon can be found in the 'Subspecies' article above. In the future we will develop a range-wide distribution article.
Habitat
Movement
Diet and Foraging
Visits mostly flowering trees (Erythrina, Inga) and shrubs (Aphelandra, Palicourea) for nectar ; many may gather in quarrelsome assemblages at flowering trees, female more often trap-lines dispersed flowers in forest; male occasionally defends territories at flowers when more aggressive species like Thalurania furcata are absent; flycatches from perches at forest edge or gaps, and gleans arthropods from foliage.
Sounds and Vocal Behavior
Quite vocal. Song rather variable, a repeated rhythmic phrase, often starting with a burry note, followed by several very squeaky or scratchy notes, and ending with repeated chips. Calls include a drawn-out metallic trill and shorter chipping notes.
Breeding
Birds in breeding condition Jun–Nov in E Colombia, but season stated to be Jan–Apr in W Brazil (2). During breeding season males usually in leks of 5–10, occasionally solitary. Clutch size two eggs, size 14–14·3 mm × 9 mm, mass 0·47 g (2); incubation period stated to be 14 days and fledging period 28 days (2). No further information.
Conservation Status
Not globally threatened (Least Concern). CITES II. Fairly common, at least locally, in foothill areas of Colombia and Venezuela, but relatively rare in Amazonian lowlands far from the Andes. In Colombia, known to use disturbed and fragmented forests.