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Butcherbird
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| Butcherbirds | |
|---|---|
| Two grey butcherbirds | |
| Scientific classification | |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Aves |
| Order: | Passeriformes |
| Superfamily: | Malaconotoidea |
| Family: | Artamidae |
| Genera | |
|
Melloria | |
Butcherbirds are songbirds closely related to the Australian magpie. Most are found in the genus Cracticus, but the black butcherbird is placed in the monotypic genus Melloria. They are native to Australasia.
Taxonomy
[edit]Together with three species of currawong and two species of peltops, butcherbirds and the Australian magpie form the subfamily Cracticinae in the family Artamidae. (Despite the name of the Australian magpie, this family of birds is not closely related to European magpies, which are members of the family Corvidae.)
Description
[edit]Butcherbirds are large songbirds, being between 30 and 40 cm (12–16 in) in length. Their colour ranges from black-and-white to mostly black with added grey plumage, depending on the species. They have a large, straight bill with a distinctive hook at the end which is used to skewer prey. They have high-pitched complex songs, which are used to defend their essentially year-round group territories: unlike birds of extratropical Eurasia and the Americas, both sexes sing prolifically.[1] the young are more brown.
Feeding and distribution
[edit]Butcherbirds are insect eaters for the most part, but will also feed on small lizards and other vertebrates. They get their name from their habit of impaling captured prey on a thorn, tree fork, or crevice. This "larder" is used to support the victim while it is being eaten, to store prey for later consumption, or to attract mates.
Butcherbirds are the ecological counterparts of the shrikes, mainly found in Eurasia and Africa, which are only distantly related, but share the "larder" habit; shrikes are also sometimes called "butcherbirds". Butcherbirds live in a variety of habitats from tropical rainforest to arid shrubland. Like many similar species, they have adapted well to urbanisation and can be found in leafy suburbs throughout Australia. They are opportunistic, showing little fear and readily taking food offerings to the point of becoming semi-tame.
Breeding
[edit]Female butcherbirds lay between two and five eggs in a clutch,[2] with the larger clutch sizes in more open-country species. Except in the rainforest-dwelling hooded and black butcherbirds,[3] cooperative breeding occurs, with many individuals delaying dispersal to rear young.[4] The nest is made from twigs, high up in a fork of a tree. The young will remain with their mother until almost fully grown. They tend to trail behind their mother and "squeak" incessantly while she catches food for them.
Species
[edit]- Genus Melloria
- Black butcherbird (Melloria quoyi)
- Genus Cracticus
- Grey butcherbird (Cracticus torquatus)
- Silver-backed butcherbird (Cracticus argenteus) - alternately a subspecies of C. torquatus
- Hooded butcherbird (Cracticus cassicus)
- Tagula butcherbird (Cracticus louisiadensis)
- Black-backed butcherbird (Cracticus mentalis)
- Pied butcherbird (Cracticus nigrogularis)
-
Black butcherbird with the remains of a wing in Cairns, Australia.
-
Eating a rhinoceros beetle
References
[edit]- ^ Johnson Gayle; "Vocalizations in the Grey Butcherbird Cracticus torquatus with Emphasis on Structure in Male Breeding Song: Implications for the Function and Evolution of Song from a Study of a Southern Hemisphere Species"; PhD Doctorate; Griffith University, 2003
- ^ Jetz, Walter; Sekercioğlu, Cagan H. and Böhning-Gäse, Katrin; "The Worldwide Variation in Avian Clutch Size across Species and Space" Supplementary Material S4
- ^ Coates BJ (1990) The birds of Papua New Guinea including the Bismarck Archipelago and Bougainville: Volume II. Passerines. Dove Publications: Alderley, Queensland
- ^ Rowley, Ian (1976); "Co-operative breeding in Australian birds" in Proceedings of the 16th International Ornithological Congress. (ed. Frith HJ, Calaby JH) pp. 657–666. Australian Academy of Science: Canberra.
External links
[edit]- Butcherbird videos on the Internet Bird Collection
Butcherbird
View on GrokipediaTaxonomy and Classification
Taxonomic History
The taxonomic history of butcherbirds reflects early European ornithologists' initial placement of these Australo-Papuan songbirds within familiar Old World groups, followed by progressive refinements based on morphology and, later, molecular evidence. The grey butcherbird (Cracticus torquatus), a representative species, was first described by English ornithologist John Latham in 1801 as Lanius torquatus in the Index Ornithologicus Supplementum, grouping it with true shrikes (Laniidae) due to superficial similarities in bill structure and predatory habits. Similarly, other butcherbird species were described around the same time as shrikes. The pied butcherbird (Cracticus nigrogularis) was first described by John Gould in 1837 as Vanga nigrogularis.[2][6] In the 19th century, Australian naturalist John Gould advanced the taxonomy by recognizing butcherbirds' unique adaptations, including their robust bills, social behaviors, and vocalizations, which distinguished them from Eurasian shrikes. Gould reclassified them into the newly proposed family Cracticidae in his seminal work The Birds of Australia (1840–1848), elevating the group to family rank and establishing genera like Cracticus for most species.[7] This separation from Laniidae was further supported by detailed anatomical studies, such as those by Dean Amadon in 1952, who provided taxonomic notes affirming Cracticidae as a distinct Australasian lineage while debating species boundaries within it.[8] Modern revisions have incorporated molecular phylogenetic data to refine relationships within Cracticidae, revealing deeper divergences and prompting generic separations. For instance, the black butcherbird is now placed in the monotypic genus Melloria, while the peltops species (Peltops montanus and P. blainvillii) form a distinct New Guinean genus, supported by analyses of mitochondrial and nuclear DNA that highlight their basal position relative to other cracticids. The hooded butcherbird remains in Cracticus.[9] These studies, including Kearns et al. (2013), also integrate the Australian magpie (Gymnorhina tibicen) into the phylogeny, often nesting it within butcherbirds and challenging traditional generic limits to ensure monophyly.[10] As of 2019, the former family Cracticidae has been merged into the family Artamidae (woodswallows, butcherbirds, and allies), with butcherbirds placed in the subfamily Cracticinae.[11] Ongoing debates center on the monophyly of Cracticinae and its potential expansion to include Australian mud-nesters (Grallina spp., family Grallinidae), which share mud nest-building behaviors but differ in ecology and morphology. Molecular phylogenies of the Corvoidea, such as Jønsson et al. (2011), confirm Cracticidae (now Cracticinae) as monophyletic within a broader Australo-Papuan radiation originating in the proto-Papuan archipelago, but place Grallina in a sister clade, rejecting close inclusion based on genetic distances and supporting separate familial status.[12] This resolution underscores the role of molecular data in clarifying historical morphological convergences.Phylogenetic Relationships
Butcherbirds belong to the subfamily Cracticinae within the family Artamidae, order Passeriformes, positioned in the diverse Corvides clade of the oscine suborder, which encompasses a wide array of Australasian and Indo-Pacific songbirds. This placement reflects the family's integration into the core corvoid radiation, characterized by adaptations to varied ecological niches in the region. Comprehensive phylogenomic analyses, incorporating extensive multilocus data, have solidified Artamidae's position as a distinct lineage within this clade, distinct from more northern-hemisphere-dominated groups like the Corvidae. DNA-based studies from the mid-2000s onward have clarified sister group relationships, revealing Artamidae's close ties to bellmagpies (such as the Australian magpie, Gymnorhina tibicen)—now included within the family—and a sister relationship to the mud-nesters (family Grallinidae, including the magpie-lark, Grallina cyanoleuca). These analyses demonstrate that Cracticinae forms a monophyletic assemblage within Artamidae, nested within the broader Australo-Papuan corvoid assemblage alongside Grallinidae, supported by shared morphological and genetic synapomorphies. Multigene phylogenies highlight how these groups diverged through vicariant events tied to geological changes in the proto-Papuan region, emphasizing their evolutionary cohesion. Evidence from mitochondrial cytochrome b gene sequences has been pivotal in confirming the monophyly of Cracticinae, with high bootstrap support in early molecular datasets showing no paraphyly among butcherbirds, currawongs, and magpies. These genetic markers, combined with nuclear loci, resolve internal relationships, such as the sister status of butcherbird genera (Cracticus) to currawongs (Strepera), underscoring the family's unified evolutionary history. Such analyses have rejected earlier morphology-based hypotheses of polyphyly, establishing Cracticinae as a robust clade. Molecular phylogenies further indicate that the divergence of the Artamidae lineage from corvids occurred around 20-25 million years ago in Australasia, aligning with the Oligocene-Miocene radiation of core Corvides amid tectonic uplift and habitat fragmentation. Divergence time estimates, calibrated using fossil constraints, place the stem age of Artamidae within this timeframe, marking an early split that facilitated its endemic diversification in the region.Physical Description
Morphology and Size
Butcherbirds of the genus Cracticus display variation in size across their six recognized species, with body lengths generally ranging from 25 cm in the black-backed butcherbird (C. mentalis) to 35 cm in the hooded butcherbird (C. cassicus), and weights from about 70 g to 160 g. The closely related black butcherbird (Melloria quoyi, sometimes classified within Cracticus) extends this range further, achieving lengths up to 44 cm and weights of 148–220 g. These dimensions contribute to their stocky, medium- to large-sized songbird morphology, adapted for a predatory lifestyle in diverse Australasian environments.[13][14][15][16] The overall build is robust, featuring a strong, muscular body supported by powerful legs and feet suited for perching on branches and shrubs, as well as walking or hopping on the ground during foraging. Their bills are a defining anatomical feature: large, thick-based, and sharply hooked at the tip, these structures are specialized for capturing, killing, and dismembering vertebrate and invertebrate prey by tearing flesh efficiently. This hooked design, combined with a thick neck, allows butcherbirds to handle prey larger than their own head size.[17][3] Wings are moderately long and rounded, with spans varying from around 35 cm in smaller species to up to 51 cm in larger ones like the pied butcherbird (C. nigrogularis), facilitating agile aerial pursuits and short bursts of flight. Tails are typically square to slightly rounded, providing stability and precise control during maneuvers in wooded habitats. Sexual dimorphism primarily manifests in body size, with males averaging 10–15% larger than females in length and mass, though both sexes share similar proportions in bill and leg structure.[18][19]Plumage Variations
Butcherbirds in the genus Cracticus typically exhibit predominantly black-and-white plumage, characterized by bold contrasts such as black hoods, wings, and tails against white underparts and wing patches.[2] This pattern is evident in species like the pied butcherbird (C. nigrogularis), where the back is mostly black with large white patches on the wings and rump.[3] Similarly, the hooded butcherbird (C. cassicus) displays a striking black hood and upperparts with white underbody and wing markings.[20] Certain Cracticus species incorporate grey tones into their plumage, providing subtler variations from the stark bicolored scheme. The grey butcherbird (C. torquatus), for instance, features a black head sharply separated from a bright white throat, with grey upperparts and black wings accented by white panels.[21] The silver-backed butcherbird (C. argenteus), a close relative, shows a paler silver-grey back in contrast to the black backs of other congeners.[22] Juveniles of Cracticus species differ markedly from adults, often displaying duller, mottled brown plumage that transitions through molts. In the pied butcherbird, young birds resemble adults in overall pattern but have browner tones, including a paler eyebrow and mottled brown areas instead of pure black.[2] The hooded butcherbird juvenile similarly features black feathers tipped with brown on the head, breast, back, and wing-coverts, along with a grey bill that darkens with age.[14] Geographic variations in plumage occur across Cracticus populations, particularly in arid regions of Australia, where paler forms adapt to environmental conditions. For example, the subspecies C. nigrogularis picatus of the pied butcherbird has a broader white collar, brighter white rump, and reduced grey on the rump compared to nominate forms, reflecting adaptations in drier inland areas.[2] In arid-adapted species like the silver-backed butcherbird, lighter grey back coloration distinguishes northwestern populations, correlating with range expansions in Pleistocene glacial maxima.[22]Distribution and Habitat
Geographic Range
Butcherbirds of the genus Cracticus are endemic to the Australasian region, with their distributions centered on Australia and New Guinea, extending to nearby island archipelagos such as the Louisiade group off southeastern New Guinea. No species occurs west of Wallace's Line, the biogeographic boundary separating the Oriental and Australasian faunal realms, underscoring their evolutionary ties to the Australian continental plate and its associated islands. This restricted range reflects historical barriers to dispersal, including deep ocean trenches and climatic gradients that have limited westward colonization into Asian mainland and island ecosystems. The current distributions of several species trace back to Pleistocene glacial cycles, during which expanded arid and savanna habitats facilitated range shifts. Arid-adapted taxa, including the grey butcherbird (C. torquatus), silver-backed butcherbird (C. argenteus), and black-backed butcherbird (C. mentalis), underwent significant expansions during the Last Glacial Maximum around 18,000–23,000 years ago, when cooler, drier conditions across Australia created contiguous suitable areas. The grey butcherbird, for instance, expanded northwestward, leading to secondary contact and genetic introgression with the silver-backed butcherbird across a former ~900 km gap of desert and savanna; its effective population size increased approximately tenfold during this period. In contrast, the silver-backed and black-backed species showed minimal range changes, maintaining stability in their core monsoon-influenced savannas. Post-glacial warming contracted these ranges, isolating populations and contributing to current patterns of endemism. Species-specific ranges vary markedly in extent and overlap. The grey butcherbird occupies the broadest Australian distribution, spanning mid-eastern Queensland southward through temperate and semi-arid zones to Tasmania and westward to northern Western Australia, with a disjunct population in the Kimberley and northern Northern Territory. The pied butcherbird (C. nigrogularis) is widespread in open eucalypt woodlands across northern, central, eastern, and western Australia, divided into subspecies nigrogularis (eastern) and picatus (northern and western). The silver-backed butcherbird is more localized, confined to drier savannas in the Kimberley region of northwestern Australia and marginally into the northwest Northern Territory. The black-backed butcherbird bridges Australia and New Guinea, occurring on Queensland's Cape York Peninsula and in the Trans-Fly lowlands of southern New Guinea from Merauke eastward to Balimo and the southeast peninsula. New Guinea hosts additional diversity, with the hooded butcherbird (C. cassicus) distributed across lowland and foothill forests of the mainland and offshore islands including the Trobriand and D'Entrecasteaux archipelagos. The Tagula butcherbird (C. louisiadensis, sometimes treated as a subspecies of the hooded) is restricted to four islands in the Louisiade Archipelago, where it inhabits tropical rainforests. Population densities in optimal habitats reflect territorial behavior, with estimates of 0.14–0.53 individuals per hectare (equivalent to 14–53 per km²) for the Tagula butcherbird across its range;[23] mainland species like the grey maintain large effective population sizes of 57,000–396,000, indicating robust abundances in suitable woodlands despite local variations.Habitat Preferences
Butcherbirds of the genus Cracticus exhibit a strong preference for open habitats that provide ample visibility and elevated perches, such as woodlands, savannas, and scrublands with scattered trees. These environments allow for effective scanning of the ground for prey, with species like the Grey Butcherbird (C. torquatus) commonly occupying eucalypt-dominated open forests and woodlands across temperate and semi-arid regions of southern Australia.[24] Similarly, the Pied Butcherbird (C. nigrogularis) thrives in tropical and subtropical open woodlands and savannas throughout northern and central Australia, favoring areas with sparse vegetation that facilitate hunting from vantage points.[25] The genus demonstrates remarkable adaptability to a wide range of climates, from semi-arid and arid zones in Australia to tropical regions in New Guinea and nearby islands. For instance, the Silver-backed Butcherbird (C. argenteus) inhabits riparian forests and edges of monsoon woodlands in northern Australia's tropical savannas, while the Hooded Butcherbird (C. cassicus) is associated with lowland second-growth forests and rainforest openings in New Guinea's humid tropics.[26][14] This versatility enables butcherbirds to exploit diverse ecological niches, though they generally avoid dense, closed-canopy forests that limit perch availability and visibility.[24][25] Elevated perch sites, such as dead branches, exposed limbs, or fence posts, are critical to their habitat selection, serving as platforms for observation and prey capture. The Grey and Pied Butcherbirds, for example, routinely utilize such structures in open scrublands and woodlands to monitor surroundings, underscoring their reliance on habitats with structural diversity rather than uniform density.[24][25] Butcherbirds have successfully colonized human-modified landscapes, including suburban gardens, farmlands, and urban fringes, where scattered trees and artificial perches mimic natural preferences. Populations of the Pied Butcherbird, in particular, are supported in agricultural areas and parks across northern Australia, benefiting from proximity to human settlements that provide supplementary resources without dense vegetation.[25] The Hooded Butcherbird similarly frequents gardens and forest edges near villages in New Guinea, highlighting the genus's tolerance for anthropogenic disturbance in otherwise suitable open habitats.[14]Behavior and Ecology
Foraging Strategies
Butcherbirds maintain a predominantly carnivorous diet, focusing on insects such as beetles, caterpillars, ants, and cockroaches, alongside small vertebrates including lizards, frogs, small birds, and mammals, with occasional consumption of carrion and fruit to supplement their intake.[27][3][28] This varied prey selection reflects their opportunistic nature, allowing adaptation to available resources in woodland and open habitats. The species' name derives from their distinctive "butcher" behavior, where captured prey is impaled on thorns, spines, barbed wire, or branch forks to form larders that aid in storage, tenderizing, or dismembering larger items for consumption.[29][18][28] These larders not only facilitate feeding by securing struggling or tough prey but also serve as caches for future meals, particularly during periods of abundance.[30] Foraging employs a range of techniques, primarily the perch-and-pounce method, where birds scan from elevated perches before dropping onto ground prey, alongside aerial sallying to intercept flying insects and occasional ground pursuits by hopping or running.[27][31][32] Activity peaks at dawn and dusk, aligning with heightened prey vulnerability, though foraging occurs throughout daylight hours, often solitarily or in pairs with brief cooperative elements in family groups.[27][33] Seasonal dietary shifts occur in response to prey availability, with vertebrates like lizards becoming more prominent in autumn.[34] For instance, in grey butcherbirds, beetles remain dominant year-round but peak in winter, illustrating opportunistic adjustments to environmental fluctuations.[34]Social Interactions
Butcherbirds, particularly species in the genus Cracticus such as the pied butcherbird (C. nigrogularis) and grey butcherbird (C. torquatus), typically live in stable pairs or small family groups that maintain year-round territories defended against intruders by all members. These territories often span 13–22 hectares in the case of the pied butcherbird, varying with habitat quality and resource availability, and are actively patrolled through vocalizations and displays to assert dominance and exclude rivals.[2] Group cohesion strengthens territorial boundaries, with family units coordinating patrols and boundary disputes to minimize incursions from neighboring groups. Several butcherbird species exhibit cooperative breeding, where non-breeding helpers—often retained offspring from previous seasons—assist the breeding pair in territory defense and provisioning young with food. In the pied butcherbird, helpers contribute to mobbing potential threats and delivering prey to nestlings, enhancing overall reproductive success in resource-variable environments.[35] Similarly, the grey butcherbird shows facultative cooperative breeding, with occasional helpers observed aiding in nest defense and chick feeding during the breeding season, though such assistance is less consistent than in strictly communal species.[36] Communication plays a central role in social interactions, with vocal mimicry allowing butcherbirds to incorporate sounds from other species, environmental noises, or even mechanical sources into their repertoire, potentially serving to deceive intruders or signal to mates within the group.[37] Alarm calls are particularly important for coordinating group responses to predators; for instance, the grey butcherbird produces distinct referential alarm calls that elicit context-specific antipredator behaviors, such as mobbing, from group members and sometimes neighboring birds.[38] In urban settings, butcherbirds frequently interact boldly with humans, approaching closely to scavenge food scraps or even accepting handouts, though they may become aggressive during breeding periods to protect territories. This adaptability enables them to thrive in human-modified landscapes, often sharing space with other species like noisy miners while maintaining social hierarchies within their groups.[39]Reproduction and Breeding
Mating Systems
Butcherbirds in the family Cracticidae predominantly exhibit monogamous mating systems, with pairs forming strong, often lifelong bonds that facilitate territory defense and biparental care. In species such as the grey butcherbird (Cracticus torquatus), pairs maintain these bonds year-round, reinforced through coordinated vocalizations and shared responsibilities during breeding.[40][18] Courtship in most species involves elaborate displays, including synchronized antiphonal duets where males and females alternate calls to strengthen pair bonds and advertise territory ownership. These duets are particularly prominent in the early breeding period for species like the pied butcherbird (Cracticus nigrogularis) and grey butcherbird, serving both as pair reinforcement and a deterrent to intruders. Aerial chases also feature in courtship rituals, with pairs engaging in synchronized flights to demonstrate agility and coordination.[18][41] While monogamy is the norm across the family, breeding seasons align with environmental cues, typically occurring in spring for Australian species from August to December, allowing pairs to exploit peak insect abundance for provisioning young. In tropical regions like New Guinea, breeding may extend year-round but peaks during the wet season.[3][42]Nesting and Rearing
Butcherbirds build cup-shaped nests primarily from sticks and grass, often reinforced with bark, rootlets, and softer linings such as fur or feathers, and position them in the forks of trees at heights typically ranging from 3 to 15 meters above the ground.[29][27][17] These nests are constructed mainly by the female, though both parents may contribute materials, providing a sturdy platform for breeding in forested or woodland environments.[18] Females lay clutches of 2 to 5 eggs, with incubation lasting 19 to 26 days by the female, during which the male frequently supplies food to the incubating female.[27][43][30] The eggs are pale with dark spots, and this biparental involvement helps maintain consistent warmth and protection against environmental fluctuations.[18] Chicks hatch and remain in the nest for a nestling period of 4 to 6 weeks before fledging, after which both parents—and sometimes older offspring acting as helpers—continue to feed and protect them for up to 3 months until independence.[18][30][43] This extended post-fledging care supports the young birds' development of foraging skills and survival in territorial groups. Stable mating pairs enhance these rearing efforts by coordinating defense and provisioning.[44] Nest predation poses a significant threat to butcherbird broods, with rates often high due to predators like currawongs and crows, prompting pairs to renest multiple times in a single season if the initial attempt fails.[45][46][47] Such adaptive renesting behaviors increase overall breeding success in response to these pressures.[48]Diversity and Species
Species Overview
The butcherbirds comprise 7 species in the family Cracticidae, distributed across two genera: Cracticus (6 species: pied, grey, silver-backed, black-backed, hooded, and Tagula butcherbirds) and Melloria (1 species: the black butcherbird).[49][1] These species are characterized by robust, hook-tipped bills and predominantly black-and-white plumage adapted for impaling prey. Shrikethrushes (Colluricincla spp.), sometimes confused with butcherbirds due to superficial similarities, belong to the unrelated family Pachycephalidae and are excluded here.| Common Name | Scientific Name | Length (cm) | Primary Distribution |
|---|---|---|---|
| Pied butcherbird | Cracticus nigrogularis | 35–40 | Australia |
| Grey butcherbird | Cracticus torquatus | 30–35 | Australia (including Tasmania) |
| Silver-backed butcherbird | Cracticus argenteus | 28–32 | Northern Australia, southern New Guinea |
| Black-backed butcherbird | Cracticus mentalis | 30–35 | New Guinea |
| Hooded butcherbird | Cracticus cassidix | 32–35 | New Guinea |
| Tagula butcherbird | Cracticus louisiadensis | ~28 | Louisiade Archipelago (Papua New Guinea) |
| Black butcherbird | Melloria quoyi | 38–44 | Northern Australia, New Guinea, Aru Islands |
