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Squacco Heron Ardeola ralloides Scientific name definitions

Albert Martínez-Vilalta, Anna Motis, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated March 18, 2017

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Field Identification

42–47 cm; 230–370 g; wingspan 80–92 cm. Over most of its range, this species is the only Ardeola. Appears mainly brownish buff at rest, but extensively white wings , rump and tail become strikingly apparent as soon as bird takes flight  . In breeding plumage has yellow-buff or straw-coloured crown, the feathers slightly or very elongated, golden to cinnamon-buff plumes  on lower neck and back , reddish-gold foreneck and breast, pinkish-brown back, with long golden plumes, and rest of plumage white. Bare parts brighter during courtship, when legs can be reddish  (soon fading to pink and back to dull yellow-green), bill bright blue with dark tip (pale greenish yellow with black tip and maxilla in non-breeding season), lores  blue (at other times yellow-green) and eyes rich yellow (paler at other times) (1). Sexes alike. Non-breeding adult dull brown with dark and light streaks, as in other members of Ardeola, with real potential for confusion with A. grayii (which is seemingly regular visitor to SE Arabia) and to lesser extent with A. bacchus, which has so far only been recorded in same range as present species as an escape (2). On Madagascar, also overlaps with A. idae, from which is easily distinguished in breeding plumage by its predominantly tawny (rather than mainly white) plumage, whereas in non-breeding plumage it is separated by being paler, less heavily streaked, with a smaller bill and narrower wings. Smaller and slighter than Bubulcus ibis, which always looks much whiter than present species, has less pointed bill and an obvious jowl, while all Ardeola have much faster and more fluttering flight than small egrets. Juvenile similar to non-breeding adult, but drabber, with more heavily streaked neck, no plumes on crest or back, dark-tipped bill, grey (rather than white) underparts and brown-tinged flight feathers (1). Race paludivaga considered to be darker and more saturated in breeding plumage than nominate, but distinction is reportedly very difficult. Birds on Madagascar average smaller than those in mainland Africa and Eurasia, but variation not recognized subspecifically (3).

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.

Closely related to A. grayii, A. bacchus and A. speciosa. Two subspecies recognized.

Subspecies

Monotypic.

Distribution

SW & C Europe (N to France and Germany) eastwards to region of Aral Sea and SE Iran; also Africa N & S of Sahara S to Cape Province, as well as Madagascar.

Habitat

Wide variety of preferably freshwater wetland habitats, including swampy plains, river valleys, deltas, lakes, ponds, canals, ditches and paddyfields, especially in areas with abundant covering of marsh vegetation and still or slow-flowing waters (4). Rare in coastal areas, including estuaries, inshore reefs or islets, but birds on Fernando de Noronha, Brazil, appear to regularly forage on tidal wave platforms. Generally in lowlands, although has bred on montane lakes at altitude of up to 2000 m, with single record at 2300 m in Malawi (5).

Movement

Palearctic populations migratory and dispersive: in Europe, post-breeding dispersal of juveniles from Jul, with birds moving on to winter quarters in Aug–Nov, migrating S across Mediterranean on broad front, mainly to sub-Saharan Africa, with occasional winter records in W Morocco, Mediterranean Basin (N to France, Spain and Italy) (6, 7) and Middle East (4); return to colonies in Apr–May, with depature from Africa commencing in Feb (1), and some birds overshooting (see Family Text), with records from Iceland, British Isles, Belgium, Luxembourg, Netherlands and Scandinavia, among others (4). Southernmost recovery of Eurasian breeder in Africa was Russian-ringed bird at L Albert (Uganda/Congo border) (8), while a juvenile ringed in Azerbaijan was recovered in Ethiopia (3120 km) (9). African populations mostly sedentary with some local movements; birds from Madagascar regularly cross over to Africa. Accidental from Azores to Cape Verde Is, Príncipe (Jul 2012) (10), in the Comoros (records on four islands) (3), on Mauritius (May 1872) (3) and the Seychelles (five records, Sept–Nov and Jan) (11, 3), as well as recently in Brazil (on Fernando de Noronha, in Jun 1986, Nov–Dec 2004, Oct 2005 and Jan–Mar 2008) (12, 13, 14) and on St Helena (Aug–Dec 2012) (15).

Diet and Foraging

Mainly insect larvae (mayflies, dragonflies and flies) (1), with some fish (Scardinus, Cyprinus, Carassius, Rhodeus, Alburnus, Lipomis, Tinca, Leiciscus, Abramis, Anguilla) (1) and amphibians (<em>Rana</em> , Hyla and Bombina frogs  and their tadpoles) (1); generally small prey  , up to 10 cm long; also amphipods (1), grasshoppers, beetles, earthworms (1), butterflies, spiders, crustaceans  , molluscs, lizards (Lacerta), snakes (Natrix), mammals (Sorex) (1) and exceptionally small birds (e.g. Sylvia warblers and Anthus pipits), once even attempting to prey on a Wood Sandpiper (Tringa glareola) (1). Principal constituents in diet vary geographically, with insects most important in Russia, fish in Italy, frogs in France, while insects are main prey in rice fields (1). Recent two-year study of nestling diet in S France found significant changes in composition since 1970s; currently it is dominated by insects (92% and 70% by biomass in 2000 and 2001, respectively), mainly Coleoptera (60% and 41%) and Orthoptera (27% in both years), while dry mass of Orthoptera, Coleoptera adults, Odonata and amphibians differed significantly between breeding sites, months and years; proportion of invertebrates (in biomass) increased from 36·5% in 1970 to 90–95% in 2000–2001, whereas the proportion of amphibians decreased from 49% and 33% in 1970–1971 to 5% and 9·5% in 2000 and 2001, respectively (16). Mainly crepuscular, but also feeds by day (ometimes selecting more open sites during early morning) (3) and occasionally nocturnally (1); generally solitary, but sometimes in small flocks of up to eight with birds well-spaced out, each defending feeding territory, during breeding season, or even larger groups on migration and in winter (1). May feed with other herons and is sometimes robbed of prey by other species (1). Normally passive feeder , hiding in vegetation and waiting for prey to approach (principal techniques are Standing and Walking Slowly , but also Standing Flycatching) (1); has been recorded using insects as bait and occasionally follows cattle in same way as Bubulcus ibis (1). Generally forages within 5 km of breeding colonies (1).

Sounds and Vocal Behavior

Considered to be mainly silent, but a shrill, harsh-sounding “karr” is mainly heard at dusk, especially during breeding season or in alarm, and also gives frog-like croaking or grunting sounds, and a rasping “kek-kek-kek-kek” in aggression (4), while bill-clappering and low cooing noises may be heard following or during copulation (1). Calls at colony generally higher pitched than those of A. idae (the two species breed together on Madagascar) (3).

Breeding

Apr–Jul in Eurasia and N Africa; mainly during rains in Africa S of Sahara (except in W Africa, where many records of nesting during dry season) (1), May in Ivory Coast (17), Mar–Jun and Aug–Sept in Ethiopia, Jan–Aug in Kenya, May in Tanzania (18), Jan–May and Aug–Oct in Zambia (peak Mar–Apr) (8), Jan–May and Jul–Dec in South Africa; Aug–Mar (peak Oct–Dec) in Madagascar (3). Seasonally monogamous and territorial, with pair-bonds forming on breeding grounds and territory confined to small area around nest (4). Usually in small or large colonies, of up to 2000 nests in Tanzania, usually with 5–10 m between nests, occasionally just 0·5 m (1); typically forms small nuclei in mixed-species colonies of other herons, especially Egretta garzetta and Nycticorax nycticorax in Europe, and Bubulcus ibis and A. idae in Madagascar, but also nests with Pink-backed Pelican (Pelecanus rufescens) (18), cormorants (Phalacrocorax), African Sacred Ibis (Threskiornis aethiopicus) (18) and Glossy Ibises (Plegadis falcinellus) (1). Nests near or over water, in reedbeds, dense thickets (e.g. of willow), or trees; generally low, less than 4 m up (but up to 20 m), and normally more effectively hidden amongst vegetation than in other herons; nest is well-constructed platform of branches, twigs or reeds (4), typically 17–23 cm wide by 5–20 cm deep, and constructed by both sexes over 6–8 days, although male is usually responsible for collecting material (1). Single-brooded (4), although double-brooding reported in Madagascar (3). Average 2–4 green-blue eggs in Africa, usually more in Europe (4–7, once 12, presumably reflecting intraspecific brood parasitism) (19), e.g. mean 4·4 at Ebro Delta (Spain), but currently only 3·2–3·3 in S France, where clutch sizes have declined during recent decades (20), laid at 1–2-day intervals, with mean size 39 mm × 28 mm in Europe, 38 mm × 29 mm in S Africa and 37·3 mm × 27·5 mm in Madagascar (1), mass 12·5–19·1 g (3); incubation 22–24 days in Europe, 15–18 days reported in Madagascar, apparently mostly by female (1); chicks hatch asynchronously and have grey, buff and white down, with yellow eyes, greenish-yellow lores, dark-tipped yellow bill and olive-green legs grading to yellow at rear (1); fledging c. 45 days, 35 days in Madagascar. Records in Madagascar and Spain of interspecific parasitism of this species by Egretta garzetta and Bubulcus ibis (19, 3). Few data on breeding success, but in Camargue (S France) 79·2% of eggs produced young and subsequent study in first region reported daily nest survival probabilities during egg and nestling periods were constant at 0·983 and 0·999, respectively, while nest survival was 0·7 and number of fledglings per breeding attempt was 1·8 (21); losses in part due to predation by raptors (1), but elsewhere young have also been observed being killed by Nycticorax nycticorax (3). First chicks to hatch generally more likely to fledge and in better condition (21). Sexual maturity generally reached at two years old, but at least one record of breeding in one-year-old bird (1). No data on longevity or mean annual survival (1).

Not globally threatened (Least Concern). In Palearctic, population has shown marked fluctuations (see Family Text ), with marked decrease between c. 1920 and 1940, due to habitat destruction and persecution (both of which threats remain current in some areas), thereafter some recovery until c. 1960 (4), and apparently mainly on increase at present with total of c. 14,300–26,800 pairs in Europe and Turkey (1), of which perhaps as many as 2500 pairs were in Romania (4): in S France, most recent estimate is of 576 pairs in 2007, when population was still increasing (22, 23); in Italy 30 pairs in 1950, 270 pairs in 1981 and 250–500 pairs in 1983–1993 (4); in Spain 100–200 pairs in 1963, up to 800 pairs in 1990 and 1032 pairs by 2006 (24). However, decreases have been recorded recently in Greece, Croatia, Bulgaria, Romania and, further afield, in Jordan (where presumed to be extinct as breeder, though may have nested in 1995) (25) and Kazakhstan (4). European Russia harbours an estimated 5000–6000 pairs, with formerly (1970) as many as c. 7000 pairs in the Volga Delta alone, but in 1990s just 300 pairs there (1), while Azerbaijan is speculated to support c. 15,000–18,000 pairs (4). Bred in Israel for first time in 1959, and estimated 100 pairs by end of 1970s, while in neighbouring Egypt species first bred in upper Nile Valley in 1970s and reached delta in 1992, when 100+ pairs were estimated (4), bred in Cyprus (26) and Syria (27) in 2004, and has also recently started breeding in C Saudi Arabia (since 1991) (28). Elsewhere in Arabia, breeding proven in Qatar in 2009 (and possibly in Bahrain the same year) (29) and perhaps in S Oman in 2012 (30). Small numbers also breed S to N Morocco and, more occasionally, Tunisia (4). In Africa, frequent or common to locally abundant, with estimated 2000–4000 birds wintering in Guinea Bissau, and 550–650 breeding pairs at Inner Delta of R Niger, Mali, where as many as 12,360 birds were counted in Jan 2001 (31); even more numerous S of equator, with an estimated 20,000 individuals in Tanzania (1). Overall, sub-Saharan African population estimated at 300,000–600,000 individuals (3). Common in Madagascar except in S, e.g. 1045 nests at Antananarivo in 1990, where species increasing at that time (1). Has been suggested that species might soon start breeding on Fernando de Noronha, in Brazilian Atlantic (14).

Distribution of the Squacco Heron - Range Map
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Distribution of the Squacco Heron

Recommended Citation

Martínez-Vilalta, A., A. Motis, and G. M. Kirwan (2020). Squacco Heron (Ardeola ralloides), 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.squher1.01
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