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Eastern Olivaceous Warbler Iduna pallida Scientific name definitions

Lars Svensson
Version: 1.0 — Published March 4, 2020
Text last updated November 17, 2017

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Field Identification

12–14 cm; 8–16 g. A grey-brown <em>Hippolais</em> with rather narrow and square-ended medium-long tail , and fairly long and pointed strong-based bill not unlike that of Acrocephalus scirpaceus. Nominate race has short and poorly marked whitish supercilium reaching back to rear edge of eye, whitish eyering; crown and upperparts uniformly warm brownish-grey or pale brown with slight rufous tinge; tertials and secondaries in fresh plumage often with paler edges (faint hint of pale panel on closed wing); tail with diffusely paler edges and tips of outer feathers; off-white below, faint buff-grey hue on breast side and flanks; iris dark brown; upper mandible largely dark, lower mandible all pinkish-yellow; legs greyish, sometimes with slight pinkish or pale brown tinge. Differs from I. rama mainly in proportionately slightly bigger head and thicker neck, longer primary projection, slightly shorter tail. Sexes alike. Immature resembles adult. Races differ mainly in tone of colour and in size: <em>elaeica</em> is largest, with longest primary projection and darkest flight-feathers, tends to be greyer above than others, often with olive tinge in fresh plumage, and to have the most pronounced pale secondary panel (fresh plumage); <em>reiseri</em> is slightly paler than nominate, pale sandy brown above, with rather obvious pale brown secondary panel; laeneni is very similar to previous, but slightly paler and smaller; alulensis is similar to last in size, but darker and greyer above, supercilium and underparts less buff-tinged.

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.

Formerly regarded as conspecific with I. opaca, but recent work has confirmed substantial differences in mitochondrial DNA (more than 9%), song, behaviour and morphology. Race laeneni poorly differentiated from, and perhaps better merged with, reiseri (1). Proposed race tamariceti (breeding E from C Turkey and Middle East) supposedly slightly paler above and shorter-billed than elaeica, but claimed differences reflect individual rather than geographical variation. Five subspecies recognized.

Subspecies


SUBSPECIES

Iduna pallida elaeica Scientific name definitions

Distribution

SE Europe (Hungary, Romania E to S Ukraine, and Slovenia and Croatia S to Greece and Bulgaria), Turkey, Cyprus, W Syria S to N Israel and W Jordan, N and S Caucasus S to Iraq, W and N Iran, E Arabian Peninsula, and from SW and S Kazakhstan E to W Xinjiang and S to Uzbekistan, S Turkmenistan and probably N Afghanistan; winters in C and E Sahel region of Africa.

SUBSPECIES

Iduna pallida pallida Scientific name definitions

Distribution

W and N Egypt, S along some of the Western Desert oases and R Nile to C Sudan; non-breeding also Sudan E to Eritrea and Ethiopia.

SUBSPECIES

Iduna pallida reiseri Scientific name definitions

Distribution

desert habitats of interior SE Morocco (2) and Algeria, possibly also Mauritania, S Tunisia and Libya (Fezzan); non-breeding also S of Sahara Desert.

SUBSPECIES

Iduna pallida laeneni Scientific name definitions

Distribution

C and SE Niger, N Nigeria, N Cameroon, Chad and (presumably this race) W Sudan.

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

Trees and tall bushes in variety of habitats: dense gardens, parks, riverine forest, often of poplars (Populus), also dense tall bushes or trees at lakesides, orchards and plantations, including of young pine trees (Pinus); also maquis of oak (Quercus), roses (Rosa), low pines, brooms (Cytisus), acacias (Acacia), and similar; also date palm oases if admixed with deciduous trees, e.g. acacias, willows (Salix), roses, Robinia, tamarisk (Tamarix), Christ’s crown (Paliurus), oaks. Prefers areas with at least some taller vegetation available; seems not to favour very low scrub and bushes. Also, often confined to areas close to water, including irrigation, but not dependent on its presence. Requires patchy, fragmented woodland with glades and much undergrowth; does not enter closed forest.

Movement

N race (elaeica) a long-distance migrant, wintering in E & NE Africa (S to L Victoria region and E Tanzania), also locally in SW Arabia; records from India require corroboration, owing to possibility of confusion with I. rama. Leaves breeding grounds mid-Jul to late Sept, passage through Middle East mainly Aug–Sept, main arrival on African non-breeding grounds from late Oct; leaves from end Mar/early Apr, some lingering until mid-May, rarely to Jun, main passage in Middle East Apr–May, and back in breeding areas from mid-Apr in S, not until May in N & E. Those breeding in N Africa (majority of nominate race and reiseri) move to areas S of Sahara, spending non-breeding season in Sahel zone or in Sudan and Eritrea region. In S of range, laeneni and alulensis, probably also S populations of nominate race and reiseri, are resident or make only shorter movements.

Diet and Foraging

Mainly invertebrates; some fruits. Invertebrates include e.g. dragonflies (Odonata), grasshoppers (Orthoptera), termites (Isoptera), bugs (Hemiptera, including aphids), moths and butterflies (Lepidoptera), various dipteran flies, ants (Hymenoptera), beetles (Coleoptera), and spiders (Araneae); larvae of beetles and butterflies taken in summer. Fruits eaten in late summer, include berries of bramble (Rubus fruticosus) and elder (Sambucus), among others. Takes prey from leaves and twigs while energetically searching the canopy; stretches its neck and picks with bill in fast movements. Will sometimes drop to the ground and take food items there. On migration, unlike at breeding sites, frequently feeds in very low scrub. Has peculiar habit, especially when foraging and moving through bushes or canopy, of repeatedly flicking or “dipping” its folded tail rapidly downwards and back again; often, each tail-dip accompanied by a call.

Sounds and Vocal Behavior

Song a fairly loud, characteristic, scratchy , monotonous phrase cyclically repeated, with low hoarse and scratchy notes followed by some higher-pitched, nasal or squeaky ones, then back to lower scratchy notes, and so on at steady, leisurely pace; notes a bit slurred, running into each other (song not “well articulated”), phrases vary between c. 10 seconds and 30 seconds, at times much longer; geographically only small variation, despite large range. Call a throaty tongue-clicking “chek” with nasal undertone, sometimes prolonged to slurred trills, “cher’r’r’r”.

Breeding

May–Jun; single brood in Europe and C Asia, possibly frequently double-brooded in Africa. Nest a well-built cup of plant stems and soft twigs, lined with plant down and fur, placed in fork of branch, commonly of tamarisk, often at 1–4m. Clutch usually 3–5 eggs; incubation by female, period 11–13 days; nestlings fed by both parents, fledge in 11–15 days.
Not globally threatened. Fairly common to common within much of its range, and locally abundant, especially in Turkey; more local in N Africa, Arabia and C Asia, owing mainly to scarcity of suitable habitats. Total European population in 1990s estimated at c. 130,000–160,000 pairs, of which great majority (c. 120,000) in Greece; c. 1,500,000 pairs estimated in Turkey. Densities can be very high in optimum habitat, e.g. 6 pairs in 0·1 ha in Cyprus; in Israel, 100 pairs in 5 km² and 47 pairs in 25 ha. Common to very common migrant in non-breeding season in Sudan, Ethiopia and Somalia; numerous non-breeding visitor also from NE DRCongo E to Kenya.
Distribution of the Eastern Olivaceous Warbler - Range Map
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  • Migration
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Distribution of the Eastern Olivaceous Warbler

Recommended Citation

Svensson, L. (2020). Eastern Olivaceous Warbler (Iduna pallida), 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.eaowar1.01
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