- Siberian Rubythroat
 - Siberian Rubythroat
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Siberian Rubythroat Calliope calliope Scientific name definitions

Nigel Collar
Version: 1.0 — Published March 4, 2020
Text last updated January 21, 2016

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Field Identification

14–16 cm; 16–29 g. Male breeding is warm olive-brown from crown to tail, with bold white supercilium and submous­tachial stripe , black lores and malar line; metallic pale ruby-red chin and throat bordered below by narrow blackish line linking malars; ashy-grey neck side and breast shading whitish on belly and buffy on flanks; bill blackish, legs greyish-flesh; male non-breeding has breast more solidly grey, bill all black. Female is like male but facial pattern less distinct, chin whitish, shading to yellow-tinged buff on throat and breast (sometimes with partly ruby throat). Juvenile is very like juvenile Erithacus rubecula or Luscinia megarhynchos.

Systematics History

Vocalizations very similar to those of C. pectoralis. Geographical variation weak and clinal; proposed E races camtschatkensis, anadyrensis and beicki considered unwarranted, although a recent DNA study recovered evidence of potentially three distinct phylo-groups according to some extent with subspecific divisions (1). Monotypic.

Subspecies

Monotypic.

Distribution

C Ural Mts and Siberia E to Anadyr, Kamchatka, Commander Is, S to N Mongolia, N Korea, N Japan and Kuril Is, also C China (NE Qinghai, SW Gansu, N Sichuan); winters in S & SE Asia, Taiwan and Philippines.

Habitat

Breeds in lowland taiga and subalpine shrubbery, clearings in forest by meadows and rivers, windfall gaps, regenerating burns with tall grass and bushes, birch coppices, clumps and stands of willow and aspen in bogs, patches of montane dwarf pine, krummholz above tree-line, overgrown forest edges and tangled thickets near mountain streams; especially in areas with fallen trees, dense bushes and stands of bird cherry (Prunus padus) and dog rose (Rosa canina), usually near fir (Abies) and spruce (Picea) stands and riverine meadows. In N Japan also in coastal grassland with bushes and scattered shrubs. In winter, found in dense thickets and scrub (notably the introduced Eupatorium odoratum in Myanmar), abandoned cultivation, bamboo brakes, dense roadside vegetation, hedges near villages, regrowth on old fields, long grass, reeds, tea gardens, town gardens, and field margins, often near streams or standing water; in duars and foothills up to 1500 m in Himalayas.

Movement

Migrant, moving through Mongolia, China, Korea and Japan to winter quarters mainly in SE Asia from NE India E to Philippines. W populations probably move E initially, to avoid high mountain ranges, before turning S; passage migrant (may occur at 4000 m) and winter visitor, Sept–Apr, in E Himalayan foothills, straggling to Rajasthan and farther S. Exodus from breeding areas starts late Aug, complete by mid-Sept in N areas and by early Oct in Transbaikalia. Main autumn passage in Mongolia Sept, in NE China (Beidaihe) mid-Sept to mid-Oct; records in Hong Kong generally end Oct to end Apr, and in Philippines Oct to early May. Reportedly abundant in S Myanmar Nov–Jan. Passage in Japan mainly late Oct to mid-Nov and late Apr to early May. Arrives back in Mongolia and in S Russian breeding range middle to late May, but in N not until late May or early Jun. Casual winter visitor to Palau. Vagrants recorded Europe , North America (Alaska), Malaysia and New Guinea.

Diet and Foraging

Insects, including flies and their larvae, ants, wasps and beetles; also plant material. In May, China, 88·5% of food consisted of insects, including beetles and mosquitoes, the rest plant matter; stomachs of E Russian birds held insects (largely beetles) and their larvae, while birds on Sakhalin I took seashore amphipods (Gammarus). Food brought to nestlings comprised adult and larval hymenopterans, adult and larval beetles, adult and larval flies, spiders, molluscs, bugs, stoneflies, adult and larval lepidopterans, an adult dragonfly and a myriapod. Forages mainly on ground , taking items from hard surfaces; also gleans from lowest parts of reeds, grass clumps and bushes. In winter quarters, noted often to be most active in twilight. Males hold winter territories.

Sounds and Vocal Behavior

Song , started before spring departure for breeding grounds, a low, rapid, musical warble comprising squeaky, chortling, jangly silvery, metallic, harsh and a few clear musical notes, with much mimicry, “chil chil chil-li chilli” and so on; more melodious than that of Cyanecula svecica, sometimes considered as fine as L. megarhynchos song. Calls include short harsh nasal “ché”, “tshuk” or “chakh” in mild (probably territorial) agitation, sometimes followed by snatches of plaintive whistling song; short musical downslurred “svee-eek” or “chee-wee”, not unlike call of Larvivora cyane; harsh churr in alarm; in Japan commonest call is “cu-ééé”, second syllable higher and stressed, and elsewhere reported as loud whistling “tiuit-tiuit”, this sometimes combined with “chakh” call as “huiit-tak-tak”.

Breeding

In Russia May–Jul, possibly Aug, main laying period early Jun and main fledging period mid-Jul; fledglings Jun in Mongolia; May–Jul in China and N Korea; Jun–Aug in Japan; single-brooded. Nest a loose cup or dome made of fine grasses and roots, usually lightly lined with hair and plant down, placed on ground in shelter of bush or dense tuft of herbage, in Japan e.g. wild rose (Rosa rugosa) and stone pine (Pinus pumila). Eggs 4–6 (3–5 in Japan), bluish-green sometimes with brown spots. No other information.
Not globally threatened. Common across extensive range in Russia, where densities variously measured include 15–26 (locally up to 40) pairs/km² in broadleaf woodland, 31–73 birds/km² in conifer and broadleaf forest, 53–61 birds/km² near glades and 31 birds/km² in riverine willows; inexplicably absent in some areas of apparently appropriate habitat. Along E coast of Moneron I (off Sakhalin) as many as 300–400 pairs/km² (3–4 pairs/ha) reported, but this highly abnormal. Rare breeding species in N Korea. Common (locally abundant) in Kuril Is and N Japan (Hokkaido, N Honshu). Numbers of autumn migrants at Beidaihe (NE China) no longer substantial, indicating possible decline over past century. In mid-20th century reportedly a great favourite with Chinese bird-fanciers owing to colourful plumage and voice, but impact of trade unknown; long considered at best uncommon in winter in S China, but possibly greatly overlooked. In winter, fairly common to common throughout most of SE Asia, but uncommon in Philippines; uncommon in winter in E Himalayas.
Distribution of the Siberian Rubythroat - Range Map
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Distribution of the Siberian Rubythroat

Recommended Citation

Collar, N. (2020). Siberian Rubythroat (Calliope calliope), version 1.0. In Birds of the World (J. del Hoyo, A. Elliott, J. Sargatal, D. A. Christie, and E. de Juana, Editors). Cornell Lab of Ornithology, Ithaca, NY, USA. https://doi.org/10.2173/bow.sibrub.01
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