- Little Bittern
 - Little Bittern
+3
 - Little Bittern (Little)
Watch
 - Little Bittern (Little)
Listen

Little Bittern Ixobrychus minutus Scientific name definitions

Albert Martínez-Vilalta, Anna Motis, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated October 18, 2014

Sign in to see your badges

Field Identification

27–38 cm (1); 59–150 g (2); wingspan 40–58 cm. Recalls other small bitterns in Africa and Asia, although very similar vagrant I. exilis must be kept in mind in W Palearctic; in Africa, principal confusion risk is I. sturmii, but present species is paler (not dark grey) and has pale wing patches; in Asia, distinguished from slightly smaller but marginally longer-billed I. sinensis by blackish (not brown) back and whitish to grey-buff (not yellow-buff) wing patches (the two species breed sympatrically in S Oman) (3, 4), and from I. cinnamomeus by dark (not cinnamon) back and cap. Male has blackish crown and modest crest, greyish face-sides, back, tail and flight feathers  also blackish, with buff-white wing-coverts  , white underwings and buffish-white underparts, sometimes with slight streaking. Lores and base of bill  range in colour from lemon-yellow to orangish yellow , sometimes flushing red  during courtship ; legs variable shade of yellow or green, typically yellow behind; eyes yellow; bill yellow or yellow-green, with dar brown culmen ridge. Female can have more contrasted plumage, more similar to that of male, but is typically smaller (2) and duller  , with a brown  or rufous  tone to dark parts of plumage, smaller and slightly streaked wing patches, and streaked underparts. Juvenile as adult female, but more heavily streaked overall, with brown-streaked crown and heavily mottled brown and buff wing-coverts. Races separated on measurements and coloration of head, neck and upperwing: payesii  smaller and shorter-winged than nominate, with neck and wing patches more red-brown to chestnut, rather than buff, irides red-brown in courtship and legs olive-green in front, yellow behind; <em>podiceps</em> smaller than both previous races (wing of male 123–133 mm, versus 149–157 mm in nominate) (5), with adult male having deep rufous on neck, underparts and underwing, and chestnut upperparts, while juvenile is darker than nominate. Extinct I. novaezelandiae, previously treated as subspecies of the present species, was larger and darker than any race of I. minutus, with dark reddish-brown mantle and scapulars, chestnut hindneck, chestnut-spotted wing patches and female was more heavily streaked below.

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.

Often considered conspecific with I. dubius (which see) and †I. novaezelandiae. Also closely related to I. exilis and I. sinensis. Races payesii and podiceps have been treated as two further species, but their morphological distinctiveness is not great, and it has been noted that nominate and payesii possess similar songs (6). Three subspecies recognized.

Subspecies


EBIRD GROUP (MONOTYPIC)

Little Bittern (Little) Ixobrychus minutus minutus Scientific name definitions

Distribution

C and S Europe and N Africa E to W Siberia and through Iran to NW India; winters in Africa.

EBIRD GROUP (MONOTYPIC)

Little Bittern (African) Ixobrychus minutus payesii Scientific name definitions

Distribution

Africa S of Sahara.

EBIRD GROUP (MONOTYPIC)

Little Bittern (Madagascar) Ixobrychus minutus podiceps Scientific name definitions

Distribution

Madagascar.

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

Very varied throughout extensive range, from dense forest to deserts; from lowlands to hills, up to 1600 m in Madagascar (5), 1660 m in Zambia (7), 1800 m in Kashmir (W Himalayas) and 2400 m in Ethiopia (8), but mainly below 500 m in W Palearctic (1) (although recorded to 2100 m on passage in Turkey) (9). For example, in E Africa, typically favours small, well-vegetated swamps, marshes and drainage ditches (10). Most commonly in freshwater marshes with reedbeds or other kinds of dense aquatic vegetation (Scirpus, Typha, Phragmites, Baumea and Juncus) (10), preferably with bushes or trees (e.g. Melaleuca, Muehlenbeckia) (10); margins of lakes, pools, reservoirs, peat bogs, oases. Also in wooded swamps, overgrown banks of streams and rivers, wet grassland and rice fields; in places, frequents mangroves and margins of saline lagoons. During migration and in winter occurs on more open waters, and even in heavily disturbed (even comparatively urban) zones, as well as dry land including fields of cereals or sugar cane.

Movement

Race minutus undergoes post-breeding dispersal in all directions, commencing Jul (1) (see Family Text ); also migrates S from Palearctic towards tropical Africa and S to Cape, wintering mostly in S & E half of continent, although southernmost populations, e.g. in N Africa and Middle East (e.g. in Saudi Arabia), can be at least partially sedentary (10, 11); migration mostly nocturnal, but can be diurnal; normally in small flocks (see Family Text ), exceptionally numbering up to c. 150 birds (12, 11), with mass migration involving 1000s of birds witnessed in autumn in N Sinai (13). Crosses Arabia and Sahara on broad front. Peak migration across N Africa in Aug–Oct and Mar–May, reaching breeding areas in C Europe and Russia in Apr to early May (1), but nominate minutus present as far S as Zambia between 11 Nov and 22 Apr (7) and Eritrea on 11 May (8). Evidence from Senegal suggests that at least some individuals return to same sites each winter (14). Birds regularly overshoot on return, with sightings N to Iceland, Faeroes (10) and Scandinavia; regularly turns up in Azores, Madeira and Canaries, with one record in Cape Verdes (15) (specimen originally thought to involve Afrotropical payesii) (16), and an exceptional record on Barbados (Dec 1995; race unknown) (17). Populations in N India, apparently resident with some local movements, and has occasionally occurred in W China (18). Race payesii performs movements connected with fluctuations in water level; straggles to Canaries. Race podiceps was reported to move from Madagascar to Africa during dry season, but based on misidentified specimens from Zanzibar, and no evidence even for intra-Malagasy movements (5).

Diet and Foraging

Varies with region and season, e.g. in South Africa, Spain and NW India, in breeding season, adults  and nestlings feed principally on fish (19, 20), but elsewhere (e.g. France, Italy) (10, 21), essentially insectivorous, taking aquatic insects and their larvae (e.g., Hemiptera (22), Libellula and Aeshna dragonflies) (10), crickets (Gryllotalpa) (10), grasshoppers, caterpillars, beetles (Notonecta, Naucoris) (10), etc. Also feeds on worms (10), spiders, molluscs, crustaceans (shrimps, crayfish) (10) and small vertebrates , including fish (e.g., Carassius, Hypopthalmichthys (22), Perca, Esox, Alburnus, Blicca, Cyprinus, Gambusia, Gobio, Eupomotis, Leuciscus) (10), frogs (Rana) (10), tadpoles , eggs (10), small reptiles  (once a c. 285 mm Balkan Green Lizard Lacerta trilineata) (23) and birds, perhaps including young Clamorous Reed-warblers (Acrocephalus stentoreus) (11). Mainly active around dawn and dusk, but also feeds during day  ; race payesii apparently more strongly diurnal, with peak activity in middle of day in South Africa. Like all Ixobrychus feeds alone, either by standing motionless or Walking Slowly (occasionally Walking Quickly) (10) partially hidden amidst vegetation; defends feeding territory (10). Bait-fishing occasionally recorded, birds using insects (e.g. dragonflies or grasshoppers) to attract fish (24). In NW India, of 123 feeding attempts recorded over three hours, at least 77 (62·6%) were successful (19).

Sounds and Vocal Behavior

Rather silent except during breeding season (1). Distinctive croaking, barking or grunting call in advertisement, far-carrying, often described as frog-like and easily drowned out by real frogs, variously rendered “kohr, kohr, kohr, kohr”, “hork, hork, hork, hork” or “gogh, gogh, gogh, gogh”, repeated at 3–5-second intervals in Madagascar (podiceps) (5); in flight, gives low-pitched and abrupt-sounding “kuk-kuk, kuk-kak”, “cuck, cuck, cuck, cuck” or more throaty “cra, a, a, a, k”, sometimes preceded by higher-pitched “quee”; a “gek, gek, gek, gek” around nest and a similar “gack” or “yick” in alarm or threat, an “aark” in anxiety, and a “goo, goo” in greeting, while young beg with “tu, tu, tu, tu” call (10).

Breeding

In W Palearctic (including N Africa) and India nesting mainly May–Jul, but probably earlier in Arabia (11) and once as early as Mar in Armenia (22); in tropical Africa season variable, generally related to rains, thus Jul–Oct in W Africa, Jun–Sept in Nigeria, May–Sept in Congo, Jul, Nov–Dec in Uganda (25), Mar–Jul in Zambia (7), Apr–May in Malawi (26), May–Jul in Zimbabwe (27), Jun–Feb in South Africa and Nov–Dec in Madagascar (5). Monogamous. Generally solitary, although sometimes forms small, loose groups in particularly favourable areas, wherein nests may sometimes be just 5 m apart, more usually 30–100 m distant (10), sometimes marginally associated with other herons such as Ardea purpurea (9) or other waterbirds, e.g. Pygmy Cormorant (Microcarbo pygmaeus) (22). Nest normally in aquatic vegetation (reeds, rushes, grasses or papyrus), often within 2–15 m of open water and just 12–150 cm above water level (22, 1, 26, 27), but alternatively low (up to 2 m above ground) (1) in bushes or trees (tea trees, alder, willow), and in E Asia occasionally high in trees over dry land; nest has conical base and is shallow platform of reeds and twigs lined with leaves or finer stems, 150–350 mm in diameter, up to 142 cm high (22) and 50–100 mm thick, constructed by male (10) over period of 4–5 days (22). May re-use same nest in subsequent season (10). In W Palearctic usually single- but sometimes double-brooded (or lays replacement clutch if first is lost) (10, 28, 29); in South Africa often two, sometimes three, albeit with smaller numbers of eggs (10) and decreasing brood size also observed in Algeria, in this case apparently in response to habitat destruction and disturbance (29). Clutch 2–9 white eggs (occasionally greenish) (1), normally 5–6 in minutus, mainly 3–4 in tropical and subtropical races, laid at intervals of 1–3 days, size 34·4 mm × 26·4 mm (Spain) (20), 29–38 mm × 21–28 mm (Armenia) (22), or 34·6 mm × 26·6 mm (South Africa) (10), mass 9·4–13·6 g (22); incubation 16–21 days, by both adults, commencing with first (10), second or third egg (22); chicks hatch asynchronously and have reddish-buff (payesii), or pink-buff (minutus) down (10), white below, with black irides, dull pink to grey bill, blue-grey to olive-yellow facial skin, and olive-grey legs and feet with pink toes (10), mean mass c. 10 g (19); fledging c. 25–30 days (1), but young leave nest after 14–16 days (10); fed mainly by female in one study (22). Hatching success 56·6% in South Africa (10), 70–71% in NW India (19), c. 87% in Algeria (29) and c. 93% in NE Spain (30), where maximum recorded fledging success was between 70% and 96% (30), and < 6% of 153 eggs were infertile or predated (20) (predation levels reached 17·6% in Algerian study) (29). One nest in Armenia also contained two eggs of Ferruginous Duck (Aythya nyroca), while another had a single Common Moorhen (Gallinula chloropus) egg, latter suspected to be result of bitterns taking over old nest belonging to the moorhen, but former might be indicative of misdirected parasitism (22). Sexual maturity in females < 2 years (10). No data on mean adult survival rates or longevity.

Not globally threatened (Least Concern). Has declined since mid-20th century in parts of W Palearctic, due to habitat destruction, pollution and perhaps also drought conditions in Africa between 1968 and 1995 (31): in Belgium, 100–200 pairs before 1960, reduced to 60 pairs by end of 1970s; in France, c. 2000 pairs in 1968, down to 250 pairs in 1990, a decline of 88%, followed by subsequent recovery to 670 pairs in 2003/04 (32, 31, 33); other obvious declines noted in Israel, Luxemburg, Netherlands (where currently increasing following 95% decline) (34), Germany, Estonia, Lithuania and Poland (1). Has occasionally bred in Britain, with first proven case in 1984 and several possible and two confirmed records since start present century, in line with increase in populations of other southern herons in UK (35, 36). W Palearctic population estimated at somwehere in excess of 37,000 pairs, with most important populations in Hungary (3500–6000 pairs), Spain (1900–2300 pairs), Italy (1000–2000 pairs), Romania (10,000–20,000 pairs), Russia (10,000–50,000 pairs, but decreasing), Ukraine (5000–6000 pairs) and Turkey (> 1000 pairs, but also declining) (1, 9). Since 1975, recognized to be scarce but regular breeder in Arabia, mainly in E, from Kuwait to S Oman, with perhaps > 500 pairs in total of which c. 200 pairs around Riyadh (Saudi Arabia) (37, 11); first proven breeding on Cyprus in 2004 (38). Frequent to uncommon in Africa, where apparently increasing in Egypt and Tunisia (1), and only recently proven to breed in Libya, but is probably regular breeder in small numbers (39); rare breeder in South Africa, probably with fewer than 100 pairs, but perhaps as many as 10,000 individuals in Tanzania (10); uncommon in Madagascar, where only known from a few localities, and population is placed at 3000–15,000 birds (5). At Haigam Rakh, in Kashmir (NW India), c. 1000–2000 breeding pairs in area of 1400 ha; records in NE Indian Subcontinent considered to be possibly erroneous, reflecting confusion with I. sinensis (40), but species has recently been discovered in breeding season as far S as Goa (41).

Distribution of the Little Bittern - Range Map
Enlarge
  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Little Bittern

Recommended Citation

Martínez-Vilalta, A., A. Motis, and G. M. Kirwan (2020). Little Bittern (Ixobrychus minutus), 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.litbit1.01
Birds of the World

Partnerships

A global alliance of nature organizations working to document the natural history of all bird species at an unprecedented scale.