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Spur-winged Lapwing Vanellus spinosus Scientific name definitions

Popko Wiersma and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated December 20, 2015

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Field Identification

25–28 cm; 127–177 g; wingspan 69–81 cm. Crown , forehead and throat black, cheeks and sides of neck white ; slight crest not normally apparent ; breast , upper belly and flanks black; dark red eyes , black spurs . Differs from wholly allopatric (1) V. duvaucelii most clearly by extensive black on underparts and shorter crest (1), while although both V. armatus and V. crassirostris (which overlap with present species in Africa) have pied head patterns, they also have obvious white (not black) crowns (1). Female as male, but spurs shorter (5–10 mm versus 8–12 mm in males) (1) and tends to have slightly browner irides (1). No seasonal variation. Juvenile (distinguishable in the field until c. Oct) (1) has black parts of plumage brownish, speckled with white; feathers of upperparts have broad buff fringes.

Systematics History

Often placed in genus Hoplopterus. Closely related to V. duvaucelii, with which sometimes considered conspecific. African populations apparently marginally shorter-winged and shorter-legged than Mediterranean ones (2), but differences considered too trivial to warrant naming of geographical races. Monotypic.

Subspecies

Monotypic.

Distribution

E Mediterranean and Middle East to SW Iran (3), and in Africa up R Nile to C & S Sudan; also S of Sahara from S Mauritania and Senegal through Nigeria to Ethiopia and Somalia, and S to Uganda, Kenya and N & E Tanzania, perhaps spreading to N Zambia (4).

Habitat

Usually on dry ground, but rarely far from water. Inhabits great variety of habitats, including cultivated fields or (burnt) grassland, near pools , lakes, rivers or lagoons, on mudflats, sandflats, sodaflats, rice fields, flooded fields, beaches and dunes. Sometimes in ponds and marshes.

Movement

In Africa resident, locally making erratic movements; in places moves into drier areas during rainy season, but leaves driest areas; in general, not very sensitive to seasonal water level changes; local numbers can vary seasonally due to movements. Egyptian population resident. Perhaps local migration in E Africa, with records S to C Tanzania (previously considered to be wanderers, although species is now known to breed in the country) (5), Congo-Brazzaville (6), N Zambia (7), Zimbabwe (8, 9, 10) Ornithological Note , Namibia Ornithological Note , Botswana (11), and even NE Cape Province, South Africa (1). Has also wandered to Cape Verde Is (Apr 2011) (12) and Príncipe (Mar 2012) (13). Populations of Greece and Turkey arrive in mid-Mar (1) and migrate S in Oct, passing through Cyprus and Crete (1), but main destinations unclear; some birds to Red Sea coast and presumably elsewhere in Africa, with recent record from Libya (14). Has also occurred W to Europe, in Bulgaria, Czech Republic, France (15), Hungary, Italy, Malta, Romania, Spain and the former Yugoslavia, as well as N to Odessa, Ukraine (1), but records from Belgium, Germany, the Netherlands and UK are considered to refer to escapes (16). Middle East population probably dispersive or resident, with records beyond usual range in Kuwait (17), Oman (1) and United Arab Emirates (17); In non-breeding season occurs in flocks of up to 15 birds, maximum 200.

Diet and Foraging

Feeds mainly on insects and their larvae, especially beetles; also grasshoppers, flies, midges, termites, ants, spiders, myriapods; occasionally, crustaceans, molluscs, small lizards, tadpoles and adult frogs, fish and seeds. Feeding action generally slow and deliberate (1): takes few rapid steps followed by stabbing at prey; also flushes prey by foot-trembling.

Sounds and Vocal Behavior

Noisy alarm calls reminiscent of those of V. armatus, a sharp metallic “pitt” or “tick”, while territorial calls are loud and rhythmic, “did-ye-do-it” or “ti-ti-ter-el”, which have been likened to those of V. indicus, albeit less raucous and more measured; often vocalizes at night (1).

Breeding

In tropical Africa, laying dates usually locally restricted, but considerable geographical variation; Israel Mar–Sept (18); Turkey early Apr–late Jun (19); Greece late Apr–May. Monogamous. Nests solitarily, e.g. one pair per 2·6 ha in Greece (20), or in loose colonies, e.g. 30 nests on single sandspit in Egypt (20). Territory aggressively defended against most other bird species, especially waders; conspecifics often tolerated in territory; territory sometimes occupied year-round. Nest on bare, dry ground, usually a shallow scrape, unlined or lined with grass or other plant material and debris, or with a rim of earth, small shells or stones; alternatively, natural depression in rock lined with pebbles; nest on mud sometimes more substantial, with grass and reed stems. Typically lays 2–4 cream to clay-coloured eggs densely spotted black, sepia or lilac (20) (mean 3·4 eggs in C Israel) (18), but up to five, size 33·9–43 × 22·2–29 mm (20), mass 35–40·7 g (21); laid at variable intervals of 1&ndash2 days or more; often lays second clutch, and sometimes third (or replacements) (18); incubation (partially commences with first egg) (20) 22–24 days (Europe, but mean 28 days in Israel) (18) and hatching asynchronous (18); both parents incubate and tend chicks, but in case of second clutch, incubation by female while male tends chicks of first clutch; chick cinnamon-buff above, mottled grey and streaked black, with cheeks buff and hindneck white, lacks hind toe; fledging 7–8 weeks, before which female may carry young under its wings (22). Immatures independent soon after fledging, but sometimes stay with parents until next breeding season. Nests and eggs often trampled by cattle and ungulates, while Hooded Crows (Corvus cornix) are important predators of eggs in some regions; if first egg of a clutch is taken the birds abandon the breeding attempt (23). In C Israel, in four-egg clutches incubation temperature significantly higher, incubation periods usually shorter (but not significantly), and hatching success higher (but again not significantly) (18). Fledging success in Israel c. 2 young per brood.

Not globally threatened (Least Concern). Probably 25,000–100,000 birds in SE Europe, SW Asia and Egypt (3). No population estimate available for rest of Africa, but 1000–5000 birds in Sudan and considered very common in Mali (although estimate of 50,000–70,000 birds regarded as over-optimistic) (24); a common bird in Israel, where 1550 birds, probably more, wintered between 1975 and 1983. Numbers have increased notably in Egypt and Israel since 1960s (e.g., five-fold increase in numbers around Gaza Strip between 1996 and 2003) (21); at least in Israel, due to new irrigation fields, reservoirs, sewage farms and control of long vegetation bordering fish ponds. Formerly considered a rare passage migrant in Lebanon, but is now common and has bred since at least 2006 (17), while in SW Iran it was regarded as a scarce winter visitor but has also recently been discovered probably breeding (3). V. spinosus is also increasing locally in Arabia, e.g. around Riyadh, where first found in 1984 and is now breeding (25), but is apparently declining in Turkey, due to wetland drainage, although it has spread further E in recent decades (19). Species endangered in Europe; first noted breeding in Greece in 1959; but numbers decreased from 120–170 breeding pairs in 1970 to 32–45 pairs in 1993, due to loss of natural or semi-natural wetland habitat of saltmarshes. Recently increased in Cyprus, where 10 pairs estimated in 2003 and 61–68 pairs in 2009 (26). Approximately 5000–15,000 birds occur in Egypt in winter. Locally exposed to hunting pressure, even in Israel, where wildlife protection laws are strong, in this case by guest workers, chiefly from Thailand (27).

Distribution of the Spur-winged Lapwing - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Spur-winged Lapwing

Recommended Citation

Wiersma, P. and G. M. Kirwan (2020). Spur-winged Lapwing (Vanellus spinosus), 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.spwlap1.01
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