Ardea poiciloptila Wagler, 1827. Syst. Av., Ardea, sp. 28: New South Wales.
The Australasian Bittern is a stocky, thick necked, medium sized, mottled dark brown and buff heron with a black mustache.
ADULT: The Australasian Bittern’s crown is brown. The upper bill is yellow to buff with the top of the bill dark brown to grey black, somewhat short relative to the New World large bitterns. The loral area is variable, green grey to blue grey, extending onto the lower bill. The irises are yellow. A narrow stripe of skin from the nostrils to the bill is dark olive brown. A light line above the eye is buff white. Side of the face is buff. A dark mustachio streak runs from the gape to the sides of the neck. It is dark brown near the bill becoming paler brown as it blends into the neck. The hind neck and back are dark brown with buff streaks and freckling giving a general mottled and streaked appearance. Upper wings are finely barred in buff and brown with dark brown flight feathers irregularly barred or spotted with buff. The tail is brown with buff fringes. Chin and upper throat is white with mottled brown central stripe. Lower throat and fore neck are buff white with dark brown longitudinal stripes and freckling. Belly and feathered thighs are white. Under wing is buff white with freckled brown. The legs and feet are green yellow to dark olive. There is no information on changes during courtship or breeding but it is likely that reported blue green lores and orange brown irises are breeding colors.
VARIATION: Females are much smaller than males but have the same plumage. However, individual plumage is highly variable. Dark, light, in-between, and red birds occur. Darker birds have a darker mustachio stripe. The upper parts are dark brown with little of the pale streaking or freckling. The dark feathers make the bird appear uniformly dark to black at a distance. Birds are also reported that are reddish, with a cinnamon buff side of face and rufous upper parts and upper wing.
JUVENILE: Immature birds are similar to adults but are paler, with a yellow tinge to the basic color, and underparts streaked rufous. Iris is yellow. Bill is yellow green to olive grey with grey brown top of bill. Facial skin is light green to green yellow, with the narrow stripe between the eye and bill being black green. The legs are dark olive.
CHICK: The hatchling has long sparse dark brown down. As they are older, they become buff to yellow brown above and yellow brown below with a white chin and throat.
VOICE: The ‘Boom” call is the loud, resonant call given during the breeding season by territorial males. They start with four short quiet gasps followed by “woomph, gasp, woom.” Each call typically includes 2 –3 booms. Males call back and forth to each other. The “Craak” call is a short harsh alarm call and also the flight call when disturbed. A bubbling sound is reported from a female returning to the nest. This and other vocalizations need more study.
WEIGHTS AND MEASUREMENTS: Length: 66 –76 cm. Weight: females 571- 1135 g; males 875 –2085 g.
The Australasian Bittern is identified by its stocky build, thick neck, medium size, brown and buff mottled plumage, plain brown crown, dark brown moustache, broadly brown streaked neck and breast, and finely vermiculated and spotted upper sides. When disturbed it flies up heavily on broad bowed wings with legs dangling, and quickly plunges back down into the vegetation without circling. In full flight, this bittern flies with steady slow wing-beats, reported to be rather owl-like (Marchant and Higgins 1990).
It is distinguished from the immature Rufescens Night Heron by being larger with a heavier, stockier build and less hunched appearance, having mottled (not densely spotted) back and upper wings. It also is not usually found in flocks nor perched in trees. Its bill is relatively shorter (shorter than length of head vs slightly longer in the night heron) (Marchant and Higgins 1990). It is distinguished from the Black Bittern by being larger, stockier, brown (not black) and upper parts. It is distinguished from the Eurasian Bittern by having darker upper parts, much darker in some, especially on the neck and back, which also are less strongly marked in paler shades.
The Australasian Bittern is one of the four large Botaurus bitterns, which all have streaked brown plumage, scutellate tarsi, 10 tail feathers, and a booming call. It is most closely related to the Eurasian Bittern (Payne and Risely 1976, Sibley and Monroe 1990). The birds of south west Australia and New Zealand in the past have been recognized as separate subspecies.
RANGE AND STATUS
The Australasian Bittern occurs in Australia, New Zealand and nearby islands.
BREEDING RANGE: The Australasian Bittern occurs in south east Australia (south Queensland, New South Wales, Victoria, east South Australia), west Australia (south Western Australia), Bass strait Islands, Tasmania, New Zealand (North Island, South Island, Stewart Island, Great Barrier Island, Mayor Island), New Caledonia and Loyalty Islands. There in fact are few records of actual breeding within this range, but it is assumed due to year-round residency.
MIGRATION: The species is generally sedentary. It likely undertakes seasonal population shifts associated with the wet and dry season, with some suggestion of winter influxes occurring along the coasts of Australia and New Zealand (Whiteside 1989, Marchant and Higgins 1990). There also appears to be movement in exceptional dry or wet situations. Dispersal occasionally occurs, perhaps more so in the past when populations were higher in New Zealand. Dispersal birds occur in Western Australia, and on islands including Chatham Island (more frequently in the past), Kapiti Island, Great Mercury Island, and Lord Howe Island, and recently in the Torres Strait (Stokes 1983), suggesting that the species should be looked for in New Guinea.
STATUS: It is widespread New South Wales, Victoria and South Australia, being most common in the Murray-Darling basin and coastal areas. In Tasmania, it is most common in east. Populations in Western Australia have decreased in the last century to about 100 pairs, and it is now confined to high rainfall areas along the west coastal plain. It is widespread but thought to be declining in New Zealand. The population there is 580 –725 birds. It was once common on the largest of the Loyalty Islands, but its current status is unclear and is likely extirpated. It is not clear if the Chatham Island population was resident or dispersive, but it has not been reported there since 1910.
New Zealand distribution maps for the species (Marchant and Higgins 1990, Heather and Robertson 1996) show it as occurring throughout the whole of the North and South Islands, which can be somewhat misleading (M. Maddock pers. comm.). There are mountains in the North Island and along the whole spine of the South Island that are up to more than 2000 m in altitude, capped with permanent snow and glaciers and heavily forested on the slopes below the snow line. However, deep valleys with lakeshore wetlands suitable for the bitterns within the habitable altitude range for the species penetrate well into the mountains. For example Chambers (1989) recommends Lakes Manapouri and Te Anau, surrounded by ranges of 1000 m or more in altitude, at the eastern margin of Fiordland, as suitable locations for observing the bird.
The Australasian Bittern typically uses permanent fresh water marshes with dense reed and rush beds situated in shallow (less than 30 cm) water. They occur along rivers, pools, lakes and swamps. They particularly use places near the edges of pools and waterways through the marsh. Typical vegetation includes Typha, Phragmites, Juncus, Baumea, Eleocharis, Gahnia, Bulboschoenus, Ludwigia, Eragrostis and small bushes. It usually feeds and nests within the marsh, near the interface of the marsh and open water. It sometimes does occur in more open situations, on mud banks and in open water. It also uses, temporary pools, tidal marsh near the mouths of freshwater creeks and seeps, mangroves (Miller and Miller 1991), rice fields, tall wet pasture, and drainage ditches (Grant and Bennett 1986). It is primarily a bird of low land swamps but occurs to 300 m in New Zealand.
The Australian Bittern is generally a solitary hunter, although it also feeds in pairs and sometimes in loose groups of up to 12 birds. It feeds primarily at night, but is also observed to feed crepuscularly and by day especially in winter. More information is needed on the daily cycle.
It feeds by Standing motionless, waiting for prey. It feeds from the edge of thick vegetation, from the bank, or from overhanging branches. It establishes feeding spots by flattening areas in the reeds, which often are littered with discarded remains of crustaceans and frogs. It also Walks slowly in a Crouched almost horizontal posture, moving forward with great deliberation, often knee-deep in water or along a bank. Each foot in turn is lifted high as it progresses. It frequently Neck Sways. It also has been recorded as Baiting using pieces of grass to lure fish.
On locating prey it makes a rapid Bill Strike by pivoting forward on its legs with neck and back straight (Whiteside 1989). The upper legs are short relative to the lower legs providing the pivot. They also Lunge from a crouched position, leaving the ground. The rapidly assume a Bittern Posture when encountering an intrusion but also uses it for surveillance (Whiteside 1989). When disturbed they fly up and return into the marsh quickly.
The diet is variable, but fundamentally fish (eels, trout, Crassius), frogs (Hyla), and crayfish (Cherax). The overall diet includes insects (cutworms, weevils, crickets, grasshoppers), spiders, mollusks, lizards, rats, mice, and small birds, including white-eye (Zosterops). In New Zealand the introduced Hyla appears to constitute its main prey. But in all areas, the diet has not been studied in any detail.
Breeding is October – February, but more information is needed. It nests in reed beds up to 2.5 m tall, usually near openings such as pools or streams. It uses small to large wetlands, 5 – 300 ha, reportedly usually only one bird per wetland. Four and five birds were reported in 200 ha swamps, or 2/ 100 ha (Marchant and Higgins 1990).
The bittern is a solitary nester. However several (up to 7) nests can be found in close proximity in the same reed bed. These are assumed to belong to one male and may represent polygamous breeding. More details are needed. The nest is a platform 30 – 40 cm across, 20 – 22 cm thick. It is made of reed and occasionally grass placed within the marsh vegetation seldom more than 10 – 30 cm above normal water level. Females appear to build the nest alone.
The male announces and advertises its territory in the spring with its Boom Call. This far carrying call is given mostly at dawn and dusk. Circle Flights have been recorded with feet dangling. A flight display has also been described involving two birds flying alternating slow flapping and gliding. It is likely the Bittern Posture is used as a display, in which the brown mustachial streak is expanded into a ruff on either side of the head and neck.
The eggs are brown olive or green cream, average 52 X 38 mm. The clutch is 4-5; range is 3-6 eggs. Incubation starts with the first egg and is 25 days. The female alone incubates.
Renesting occurs when eggs are lost. The chicks are fed by regurgitation into the nest, apparently by the female. The chicks can leave the nest in 2 – 3 weeks, and begin to wander into the surrounding reeds. They fledge in about 7 weeks. Nothing is known of the nesting success of the species.
Nothing is known of the population biology or demographics of the species.
SPECIES ACCOUNT UPDATES
Please update, add, or correct information in this species account by posting it as a comment, below. Provide a title starting with the Species’ English name followed by the most pertinent account section title, capitalized. For example: ”Agami Heron Reproduction”. Then make your update using language as close as possible to the original text so as to allow for later insertion directly into the account. Images that show the biological information being presented are welcome, especially maps that change the range information. Because these images cannot be inserted directly as a comment, the update with the images should be emailed to HeronSpecialistGroup@Earthlink.net so that they can be inserted directly by the Web Site administrators. Provide complete literature references (authors, year, title, journal, book or online reference data) following the style of the Heron Bibliography. At the end of the comment, provide the author’s full name, preferred contact information, and date of contribution in day-month-year format (For example: 21 May 2011).