Nightingale Reed Warbler Acrocephalus luscinius Scientific name definitions

Andrzej Dyrcz and Christopher J. Sharpe
Version: 1.0 — Published March 4, 2020
Text last updated June 25, 2015

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Field Identification

18 cm; male average 35·9g, female average 32 g. Relatively large reed-warbler with very long bill, head plumage often dishevelled. Nominate race has yellow supercilium, black eyestripe; crown and upperparts rusty brown, narrow buff edges on primaries and secondaries and on tips of rectrices; light yellow to cream below, flanks brownish-yellow to buff; iris dark; upper mandible greyish-black with yellow edges, lower mandible flesh-pink with yellow edges; legs greyish-blue. Sexes similar in plumage , male slightly (but significantly) larger than female. Juvenile undescribed. Race nijoi has shorter bill than nominate, also upperparts much less rusty, flanks and belly darker and more brownish.

Systematics History

Has sometimes been treated as conspecific with A. syrinx, and sometimes also with A. rehsei, but differed from both in distinctly larger size, much longer bill and song. Previously considered conspecific with †A. nijoi, †A. yamashinae and †A. astrolabii, while A. hiwae was often treated as a synonym of luscinius (sensu stricto); but all are now separated primarily on basis of comprehensive genetic data (1, 2). Monotypic.

Subspecies

Restricted to freshwater wetland and wetland-edge vegetation, this species is thought to have succumbed to a combination of predation by the introduced brown tree-snake (Boiga irregularis), wetland destruction, pesticide use and major fires. The last sighting was in 1969, and searches in the 1970s and 1980s failed to find it (3, 4, 5, 2).

Distribution

Guam, in S Mariana Is.

Habitat

Mosaics of elephant grass and tangan-tangan (Leucaena), also mangroves (Bruguiera gymnorrhiza), reed (Phragmites karka) marshes, Hibiscus thickets; also typhoon-created forest openings with meadow vegetation and thickets , and groves of trees.

Movement

Resident.

Diet and Foraging

Information sparse. Diet probably mostly insects, lizards, also spiders (Araneae) and snails. Forages mainly on ground; gleans invertebrates from leaves (both live and dead ones), and probes dead stubs.

Sounds and Vocal Behavior

Song loud , melodic, varied and complex, of whistles , warbles and trills, long sustained, may continue unbroken for several minutes; often sings at night; males sing in chorus at dawn, but singing less frequent during day. Call a loud “chuck” or “tchack”.

Breeding

Peak periods in Jan–Mar and Jul–Sept. Monogamous. Nest built by female, a rather deep cup, two types distinguished, one tightly woven and compact, the other larger and tightly woven with bulky outer material; in each case constructed chiefly of dry vine stems, also dry grass blades, dry bark strips, spider webs, petioles and branchlets, external diameter 8·3–12·7 cm (mean 1·6 cm), height 5·7–17·7 cm (9 cm), internal diameter 4·6–8·6 cm (6·5 cm), cup depth 2·9–5·8 cm (4·5 cm); in most cases built in tree (mainly the introduced tangan-tangan) at height of 2·3–10 m; average size of seven territories 9338 m², ten times larger than territories of A. orientalis. Clutch 2–4 eggs (mean 2·5); no information on incubation and nestling periods. Adult male annual survival at least 82%.

CRITICALLY ENDANGERED. Restricted-range species: present in Mariana Islands EBA. Current population estimated at c. 3700 individuals, all of nominate race: 946 on Alamagan in 2010 External link and 2742 on Saipan in 2007 (6). Nominate race extirpated on Guam, where last known sighting, of a single individual, occurred in 1969. Race yamashinae became extinct on Pagan I, to which it was confined, before 1981 (7). Race nijoi almost certainly extinct on Aguijan: has not been observed since 1995, despite extensive surveys in 2000, 2001, 2008 and 2009 (6, 8) External link . Surviving population declining rapidly: 59% decline in the three decades since 1982, and rate of decline is increasing External link . Cause is habitat loss (agriculture, home-building and tourist-related facilities), as well as predation by introduced brown tree snake (Boiga irregularis), monitor lizard (Varanus indicus), feral cats and rats (Rattus); also as a result of pesticide use and major fires. A recovery plan in progress includes programme for removal of goats (which destroy habitat) and snakes from the islands.

Distribution of the Nightingale Reed Warbler - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Nightingale Reed Warbler

Recommended Citation

Dyrcz, A. and C. J. Sharpe (2020). Nightingale Reed Warbler (Acrocephalus luscinius), 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.nigrew1.01
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