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Thrush Nightingale Luscinia luscinia Scientific name definitions

Nigel Collar
Version: 1.0 — Published March 4, 2020
Text last updated June 9, 2014

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Field Identification

16–17 cm; 14–37 g. Very like L. megarhynchos, but less bright or less contrastingly reddish on tail  and rump , greyer on back, and generally has breast diffusely mottled grey-brown; often more strongly developed malar stripe  ; outer primary greatly reduced in length (sometimes visible in field). Sexes similar. Juvenile  as juvenile L. mega­rhynchos.

Systematics History

Hybridization with L. megarhynchos rare. Monotypic.

Subspecies

Monotypic.

Hybridization

Hybrid Records and Media Contributed to eBird

  • Thrush x Common Nightingale (hybrid) Luscinia luscinia x megarhynchos

Distribution

N, C & E Europe E to N Kazakhstan and upper R Yenisey, also S Caucasus; winters in SE Africa.

Habitat

Lowland river valleys with deciduous and mixed woodland bordering waterbodies, beech (Fagus) and hornbeam (Carpinus) forest, small woodlots (less than 1 ha) of young deciduous trees, dense thickets in forest edges (notably along roads and railways), regenerating forest on clear-cut land, wet willow (Salix) thickets, alder (Alnus) carrs, lowland orchards, river gorges, urban scrub, parks, cemeteries; key requirements are for deep soft humus with some leaf litter, tall, dense, patchy herbage (including rank patches of nettles), and thickets of brambles, bushes, shrubs and low trees typically along riverbanks, near standing water or in damp depressions. In African winter quarters found in damp rank vegetation, overgrown streamsides, thick hedges of Euphorbia and Lantana, woodland undergrowth and thickets, at 500–1500 m; on passage drier and more varied habitats, such as scrub, bushland thickets, hedges and mangroves (Sudan coast), ranging to 2200 m in E Africa.

Movement

Migratory ; winters in Africa, mainly S Tanzania S to E South Africa. Very common along Red Sea coast of Sudan in autumn, but very rare in spring; common to abundant E of Rift Valley on S migration, when more than 31,000 ringed Nov–Dec in Tsavo West National Park (Kenya) 1969–1995, but less numerous from late Mar to mid-Apr. Populations from Baltic and C Europe move SE from early Aug, peak passage in Hungary mid-Aug, in Slovenia second half Aug or early Sept, skirting W shore of Black Sea and crossing E Mediterranean, passing through Israel mainly Sept, and into Egypt, rapidly through NE Sudan (where second most abundant migrant on coast Aug–Sept) to reach W & C Ethiopia, where apparently stop over for several weeks, as onward S movement through C & SE Kenya and NE & C Tanzania occurs early Nov to mid-Dec. C breeding populations presumably move S between Black and Caspian Seas (first passage in Crimea late Jul) and merge with W breeders in E Mediterranean, while at least some E breeders move down E and then S sides of Caspian from end Aug to mid-Sept, passing through Middle East and Gulf (Bahrain Sept–Oct), but main flyway into Africa unclear, perhaps involving W movement to N Red Sea area or broad-front crossing of Arabian Peninsula; considerable numbers pass along Turkish Black Sea coast mid-Aug to late Sept. Majority of autumn population assembled in Kenya moves E of Mt Kilimanjaro on a front c. 250 km wide and shifting direction from S to SSW, wintering in area from SW Tanzania S to N Botswana and N South Africa during late Nov to late Mar. Spring passage in Kenya from late Mar to mid-Apr, in Ethiopia early Apr to mid-Apr, last birds in Egypt in early May; main passage Israel mid-Apr to end May, Bahrain Apr to early May, later birds in Middle East presumed en route to E parts of breeding range (first arrivals in SC Siberia not until second half May), whereas earlier migrants probably move to W parts of breeding range, where arrival typically in first 10 days May. Vagrants regularly recorded in W Europe.

Diet and Foraging

Invertebrates  , some fruit. Summer diet includes adult and larval beetles of many families, adult and larval moths, ants, sawflies, flies, bugs, caddis flies, grasshoppers, damselflies, spiders, woodlice, millipedes and snails, with fruits of elder (Sambucus), currants (Ribes), bramble (Rubus), mulberry (Morus), vine (Vitis) and service (Amelanchier). In Armenia mainly leaf-litter insects, with small amounts of plant matter; seen to feed on mulberries in Jul. In E Germany, invertebrate content of stomachs was 53% hymenopterans (largely ants), 24% beetles (largely adults), 9% bugs, 4% earwigs and 10% others; 53% involved terrestrial species, 34% leaf-dwellers and 13% undetermined. Diet of young at same site consisted of 38% beetles (mostly larvae), 20% lepidopterans (mostly larvae), 13% flies (mostly adults), 11% woodlice, 9% spiders, 3% hymenopterans, 3% bugs and 3% others; 54% involved subsoil species, 43% were herb-layer or shrub-layer species, rest undetermined; items smaller than those taken by adults. Young in Russia fed with 29% lepidopterans (mostly larvae), 20% larval snake-flies (Rhaphidiidae), 18% spiders, 16% beetles (mostly adults), 8% bugs, 4% snails, 3% adult flies and 2% grasshoppers. In Africa mainly invertebrates, especially insects such as ants, beetles, small grasshoppers, and flies and lepidopterans at all stages, also millipedes and small molluscs; sometimes fruit and seeds. Forages mainly on ground, hopping about in leaf litter; also gleans insects from herb and shrub layers, and occasionally sallies after flying insects. Territorial in winter quarters, spacing out at c. 100-m intervals.

Sounds and Vocal Behavior

Song, regularly at night but also by day, very similar to that of L. mega­rhynchos but delivery slower, phrases longer (c. 5 seconds) and separated by longer pauses (3–5 seconds), commonly lacking protracted crescendo whistle phrase; phrases typically in three sections, starting with whistling “wiiit-wiiit-wiiit…” followed by deep fluty “chuuk-u-chuuk-u…” or “chiddy-ock-chiddy-ock-chiddy-ock” and ending with deep rattle; rarely gives (perhaps only as mimicry) slow crescendoing and accelerating one-pitch whistling phrase (“wuuuuuu-”) common in L. megarhynchos; reportedly uses mimicry, at least locally (e.g. Armenia); in confrontations song assumes strangled quality, and in courtship (also towards incubating mate, which may then sing back) becomes softer with more high-pitched units. In non-breeding quarters sings throughout period present, but on S passage song more guttural and disorganized than in spring; full song often heard Feb–Mar. Calls include guttural “tuc” or “tuc-tuc” in territorial alarm, low croaking “krrrk” in mild agitation, and whistled “wiiit”, sharper and higher than that of L. megarhynchos; first two calls sometimes combined as “tuk tuk tuk krrrrrr” in greater alarm.

Breeding

Mid-May to early Jul, perhaps somewhat later in E; single-brooded. Nest a loose bulky cup of leaves and grass, lined with fine stems and hair, placed on ground in sheltered position among dead branches, roots or thick leaf litter. Eggs 4–5, olive-green with reddish freckling; incubation period 13 days; nestling period 10 days; post-fledging dependence 2–3 weeks. Of 216 eggs in 45 nests in Finland, 86% hatched, and 89% of hatchlings fledged, giving overall breeding success of 77%. Age of first breeding normally 2 years, but some males breed as yearlings. Oldest recorded individual 8 years 11 months.

Not globally threatened. Total European population in mid-1990s estimated at 832,226–1,041,309 pairs, with additional 100,000–1,000,000 pairs in Russia W of Urals. By 2000 European population (including European Russia) revised to 3,700,000–6,900,000 pairs, and considered generally stable. Marked increase in numbers in N & W of European range in 1960s and 1980s, e.g. population in Finland rose from 200 pairs in 1950s to 20,000–50,000 pairs in 1990s; reasons presumed to include cessation of grazing and lowering of lake levels, both allowing succession involving young deciduous woodland. Uncommon in Armenia. In winter quarters locally common to abundant; uncommon to abundant on passage through E half of Africa, depending on area.

Distribution of the Thrush Nightingale - Range Map
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Distribution of the Thrush Nightingale
Thrush Nightingale, Abundance map
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Data provided by eBird

Thrush Nightingale

Luscinia luscinia

Abundance

Relative abundance is depicted for each season along a color gradient from a light color indicating lower relative abundance to a dark color indicating a higher relative abundance. Relative abundance is the estimated average count of individuals detected by an eBirder during a 1 hour, 1 kilometer traveling checklist at the optimal time of day for each species.   Learn more about this data

Relative abundance
Breeding season
Jun 21 - Jul 13
0
0.05
0.4
Non-breeding season
Dec 28 - Jan 4
0
0.05
0.4
Pre-breeding migratory season
Mar 29 - Jun 14
0
0.05
0.4
Post-breeding migratory season
Jul 20 - Nov 30
0
0.05
0.4
Note: Seasonal ranges overlap and are stacked in the order above; view full range in season maps.
Seasons timeline
Learn more about seasons

Recommended Citation

Collar, N. (2020). Thrush Nightingale (Luscinia luscinia), 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.thrnig1.01
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