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Tomtit Petroica macrocephala Scientific name definitions

Walter Boles, Josep del Hoyo, David Christie, Nigel Collar, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated April 19, 2018

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Introduction

Taxonomic note: Lump. This account is a combination of multiple species accounts originally published in HBW Alive. That content has been combined and labeled here at the subspecies level. Moving forward we will create a more unified account for this parent taxon. Please consider contributing your expertise to update this account.

Field Identification

Tomtit (New Zealand)

13 cm; 11–13 g. Male nominate race has head , neck and upperparts black, small white forehead spot ; upperwing black, white bar across bases of remiges (except outermost primary); tail  with central three feather pairs black, T4 black with distal half of inner web white, T5 white with black base, tip and distal third of outer web, T6 white with black base and broad black tip; chin, throat and upper breast black, rest of underparts pale yellow, often with brighter yellow or orange bordering sharp demarcation against upper breast; iris dark brown; bill black, legs black to dark purplish brown, feet with soles (at least) yellow to pink-brown or grey. Female is similar to male, but dark olive-brown above  , with narrow white eyering, ear-coverts finely streaked white, black of wing  and tail replaced by blackish brown, chin and throat mottled or washed dark grey, underparts yellowish white, breast often washed olive-brown. Juvenile  is duller and browner than adult, with mottling and fine streaking; immature as adult. Race <em>toitoi</em> is similar to nominate, but male has lower breast to undertail-coverts white; chathamensis  is larger, male has T4 tipped black and undertail-coverts black, female is warmer brown with dark face and black line above forehead spot; <em>marrineri</em> has lower breast and belly yellow-white, grading to off-white on flanks and vent, flank feathers tipped black, undertail-coverts black, tail variable, like that of previous or nominate or with white subterminal spot on inner web of T3, female like male but usually browner and underparts paler.

Tomtit (Snares Is.)

c. 13 cm. Adult has entire plumage glossy black , wings and tail less glossed; iris dark brown; bill  black, legs black to dark purplish brown, feet with soles (at least) orange-coloured. Sexes more or less alike, female perhaps somewhat less glossy. Juvenile is duller and browner than adult.

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.

Tomtit (New Zealand)

Hitherto treated as conspecific with P. dannefaerdi (which see). Races differ in coloration (including degree of sexual dimorphism) and voice; despite low genetic differentiation (1), species rank has been proposed for all races (for consistency with treatment accorded to mainland P. australis and insular P. traversi and P. longipes). Four subspecies currently recognized.

Tomtit (Snares Is.)

Hitherto (in recent times) considered conspecific with P. macrocephala, but differs in its all-black underparts (3); absence of white in wings and tail (3); and larger size (from published data (2), effect size for male bill against largest subspecies marrineri of P. macrocephala 2.47, score 2). Monotypic.

Subspecies


EBIRD GROUP (POLYTYPIC)

Tomtit (New Zealand) Petroica macrocephala [macrocephala Group]


SUBSPECIES

Petroica macrocephala toitoi Scientific name definitions

Systematics History

Muscicapa toitoi Lesson and Garnot, 1828, Manuel d’Ornithologie, Tome 1, p. 188.—New Zealand [= Bay of Islands, Northland] (3, 4). The name is usually attributed to Lesson alone (e.g., 5, 6, 7), but Dickinson et al. (8) recommended to treat it as co-authored by Lesson and Garnot.

Distribution

North Island and adjacent islands (Hen and Chickens, Little Barrier, Great Barrier, Kapiti), in northern New Zealand.

Identification Summary

Subspecies toitoi is similar to the nominate, but the male has the lower breast to undertail-coverts white.


SUBSPECIES

Petroica macrocephala macrocephala Scientific name definitions

Systematics History

Parus macrocephalus J. F. Gmelin, 1789, Systema Naturae, Tome 1, part 2, p. 1013; based on the ‘Great-headed Titmouse’ of Latham, 1783, A General Synopsis of Birds, Volume 2, part 2, p. 557.—Queen Charlotte Sound, Marlborough, New Zealand.

Synonyms:
Miro Dieffenbachii G. R. Gray, 1843, in Dieffenbach, Travels in New Zealand, Volume 2, p. 191.—Chatham Islands; error: the type, an adult male collected by Dr Sinclair, in the Natural History Museum, Tring (NHMUK 1842.10.30.15) (9), is from the South Island, New Zealand, fide C. A. Fleming, 1950, Transactions and Proceedings of the Royal Society of New Zealand 78:36. (3)
Turdus minutus J. R. Forster, 1844, in in M. H. C. Lichtenstein, Descriptiones Animalium quae in Itinere ad Maris Australis Terras, p. 83.—South Island.

Distribution

South Island, Stewart Island, and outlying islands (including D’Urville, Pickersgill, Resolution, Codfish and South Cape).

Identification Summary

Described under Plumages.


SUBSPECIES

Petroica macrocephala marrineri Scientific name definitions

Systematics History

Myiomoira macrocephala marrineri Mathews and Iredale, 1913, Ibis (10)1:436.—Auckland Islands.

The holotype, an adult male presented to the national collection by the Lords of the Admirality, is held at the Natural History Museum, Tring (NHMUK 1942.12.16.48) (9).

Distribution

Auckland Islands (Enderby, Ewing, Rose, Adams, Auckland), but no recent records on Rose Island, where apparently became extinct sometime between 1996 and 2013, perhaps having been out-competed by an increasing population of New Zealand Bellbird (Anthornis melanura); or on Adams Island since the 19th century (10); and Ocean Island is frequently listed as part of the subspecies’ distribution, but there are no records there (11).

Identification Summary

Differs in having in that the male has the lower breast and belly yellow-white, grading to off-white on the flanks and vent, the flank feathers tipped black, and undertail-coverts black; tail variable, like that of chathamensis or nominate, or has white subterminal spot on inner web of r3. Some observers have reported that males on the main island are much more brightly colored than those on Enderby Island (11). Female like male, but said to be usually browner and underparts paler, although Miskelly et al. (11) reported that this subspecies is monomorphic..


SUBSPECIES

Petroica macrocephala chathamensis Scientific name definitions

Systematics History

Petroica macrocephala chathamensis C. A. Fleming, 1950, Transactions and Proceedings of the Royal Society of New Zealand 78:36.—Rangatira (= Southeast) Island, Chatham Islands. (3)

The holotype, an adult male collected by Joe Hicks of the American Museum of Natural History Whitney South Sea Expedition on 15 March 1926, is held at what is now at the Museum of New Zealand Te Papa Tongarewa, Wellington (MNZ OR.001832), formerly the Dominion Museum (3).

Distribution

Chatham Islands (Pitt Island, Rangatira Island, Mangere Island, occasionally also Little Mangere Island; presumably extinct on Chatham Island).

Identification Summary

Subspecies chathamensis is larger than the nominate and toitoi, and compared to these two, male has r4 tipped black and undertail-coverts black, whilst female is warmer brown, with a dark face and black line above forehead spot.


EBIRD GROUP (MONOTYPIC)

Tomtit (Snares Is.) Petroica macrocephala dannefaerdi Scientific name definitions

Systematics History

Miro dannefaerdi Rothschild, 1894, Novitates Zoologicae 1:688.—Snares Islands.

First mentioned by Reischek (10) and Chapman (12). The lectotype, an adult male, taken by Dannefaerd and originally in the Rothschild collection, is at the American Museum of Natural History, New York (AMNH 608043); paralectotypes held at the same institution are: AMNH 608038, without further data; AMNH 608039–608042, three males and one female, collected by Travers in April 1894; and AMNH 608044–608057, five males, five females, four unsexed, undated, all from the Dannefaerd Collection (13). A further Dannefaerd specimen (also a paralectotype) was sent by Rothschild to the Rijksmuseum van Natuurlijke Historie, now the Naturalis Biodiversity Center, Leiden (RMNH 89814) (14, wherein it is listed as a syntype).

Distribution

Snares Islands (Snares Island, Broughton Island).

Identification Summary

Differs from all other subspecies in that the adult is entirely glossy black, albeit less glossed on the wings and tail. The sexes are more or less alike, but the female is perhaps somewhat less glossy. Juvenile is duller and browner than adult.

Distribution

Tomtit (Snares Is.)

Snares Is (Snares I, Broughton I).

Habitat

Tomtit (New Zealand)

Native forests, both mature and regrowth, from lowland podocarp-broadleaf to southern beech (Nothofagus) in highlands, various mixed forests and manuka (Leptospermum) and kanuka (Kunzea) scrublands; will use exotic pine (Pinus) plantations, occasionally farmland, parks and gardens. On Auckland Is , scrub and littoral vegetation and Olearia forest, nearby open turf, tussock grassland and coastal rocks; scarce above 150 m, and absent from highest areas.

Tomtit (Snares Is.)

Mainly tussock grassland with scattered scrubs.

Migration Overview

Tomtit (New Zealand)

Adults mainly sedentary, with some small-scale local or altitudinal movements; in some localities shifts to more open areas after breeding, elsewhere present throughout year. Juvenile dispersal of up to 16 km recorded. Species’ dispersal capabilities demonstrated by reoccupation of Mangere I (and sporadic occurrences on Little Mangere I), in Chatham Is. One individual translocated to an island returned 56 km to its original site.

Tomtit (Snares Is.)

Sedentary.

Diet and Foraging

Tomtit (New Zealand)

Invertebrates  , mainly insects; occasionally (especially in autumn) fruit of a range of species. Forages at all heights, although on larger islands prefers understorey of mature forest, and on small islands or in exotic vegetation often spends more time on ground. Most time spent searching for prey from elevated perch . On South I (nominate race), little time on ground (0–3%), most time in understorey (60–80%), particularly lower part, and some use of canopy (10–16%) and above (less than 5%). On Rangatira I (chathamensis), 6·7% of foraging on ground, 72·1% in lower storey, 19·2% in upper storey and 2% in canopy; on Little Barrier I (toitoi), 58·5% on ground, 34·6% in understorey, and 7·3% in subcanopy and canopy. In pine plantations, 61% of feeding on or near ground, 11% at 1–5 m, 18% at 5·1–10 m, 10% above 10 m. In one study on Rangatira I, most prey taken from ground (65%), less from bark (10%) and foliage (13%) and in air (7%); in another study on same island, much more in vegetation, i.e. trees (38·5%), branches (15·4%), twigs (26%), vines (13·5 %), foliage (1%), ground litter (5·8%). On Little Barrier I, prey taken from ground (52·4%), trunk (6·1%), branches (13·7%), twigs (4·2%), leaves (19·3%), air (4·2%). In pine plantation, most prey attacked on ground (60%), fewer on trunks (10%), branches/cones (7%) and needles (16%) and in air (7%). Regardless of whether on large or on small island, generally uses similar attack methods: pounce on ground or sally-strike (84–93%), glean (2–12%), hover (0–1%), aerial sally (3–5%). When gleaning on ground, picks visible prey from surface; does not turn leaves.

Tomtit (Snares Is.)

Invertebrates, principally insects; occasionally fruit of a range of species. When foraging spends most time (60%) less than 2 m above ground, with decreasing occurrence upwards at 2·1–4 m (27%), 4·1–6 m (10%) and above 6 m (3%). Prey taken from ground (15%), tree trunk (20%), branch (42%), twigs (20%), foliage (less than 1%). Attack methods include pounce on ground or sally-strike (84–93%), glean (2–12%), hover (0–1%), aerial sally (3–5%). When gleaning on ground, picks visible prey from surface; does not turn leaves.

Sounds and Vocal Behavior

Tomtit (New Zealand)

Song a musical warble  , “ti-oly-oly-ho” or “yodi-yodi-yodi”. Gives 1–5 “zet” notes when foraging alone, possibly as contact call; also 2–7 “seet” notes when disturbed, soft closely spaced whistles.

Tomtit (Snares Is.)

Male has a short musical warbling song. Contact calls “swee” and “seet”.

Breeding

Tomtit (New Zealand)

Season Aug–Mar on North I, Sept–Feb on South I and Oct–Dec on offshore islands; usually two or three broods in season, and up to six attempts if failures occur. Breeds as monogamous pair. Territorial throughout year, territory defended by both sexes. Courtship display involves male chasing female with wings held high and forwards, or partners facing each other while flicking both wings alternately; male feeds female during courtship, nestbuilding and incubation. Nest  built by female, a cup  of moss, leaves, rootlets, grass and bark, bound externally with spider web, lined with fine grass, feathers, fur and tree-fern scales, external diameter 10·2 cm, height 7·6 cm, internal diameter 5·7–6·5 cm, depth 3·8–4 cm; placed 1–18 m (usually 1–4 m) from ground in situation providing shelter along sides and sometimes above, such as cavity in tree or stump, tangle of vines, behind loose bark, or under crown of tree-fern; nestboxes accepted; territory 1·2–2·5 ha. Clutch 2–6 eggs  (usually 3–4) on North I and South I and 1–4 (mostly three) on Chathams, laid at 24-hour intervals, creamy white, with yellowish-purple, light brown and grey spots forming dense wreath towards larger end, size variable, 17·7 × 14·7 mm on North I, 18·2 × 14·9 mm on South I, 19·1 × 15 mm on Chatham Is, 23 × 16·5 mm on Aucklands; incubation by female, rarely assisted by male, period 14–18 days on North I and 15–17 days on South I, but 17–18 days on Chathams; young hatch mostly naked, down appearing on day 3, down-covered by day 5; chicks  brooded by female, fed  by both sexes, nestling period 17–20 days on North I, 20 days on South I and 17–21 days on Chathams; adult performs distraction display on ground, holding wings spread and raised and tail fanned while moving with jerky actions; fledglings fed by both sexes for c. 10 days after leaving nest (or by male alone if female renests immediately) and by male for a further 1–2 weeks, disperse 5–6 weeks after reaching independence. Nests parasitized by Long-tailed Koel (Urodynamis taitensis). Success quite variable: in some areas most nests attacked by predators, e.g. black rat (Rattus rattus) and Long-tailed Koel; success 80% or more in those areas where predators controlled. May breed at end of first year of life.

Tomtit (Snares Is.)

Breeds Oct–Jan; usually two or three broods in a season. Monogamous; territorial all year, territory defended by both sexes. Courtship involves male holding wings high and forwards while chasing female, or partners face each other and flick both wings alternately; male feeds female throughout courtship to incubation. Cup-shaped nest of leaves, moss, rootlets, grass and bark, bound with spider web, lined with fine grass and other soft material, placed fairly close to ground (up to 3·5 m) in sheltered site such as cavity in tree or stump, or among rocks in tussocky areas; territory size c. 0·4–1 ha. Clutch 2–3 (mostly three) eggs, creamy white, with purplish, brown and grey spots forming dense wreath towards larger end, size 20 mm × 15·2 mm; incubation by female, rarely assisted by male, period 18–20 days; young hatch mostly naked, brooded by female, fed by both sexes, nestling period 17–22 days, and young become independent when 40–54 days old. Clutch size is positively influenced by distance to nearest penguin colony, with robins closer to seabird colonies laying more eggs.

Conservation Status

Tomtit (New Zealand)

Not globally threatened (Least Concern). Locally common. Initial decline, owing to clearance of habitat and introduced predators after arrival of Europeans, appears to have stabilized, as the species adapts to modified conditions, and some evidence of local increases in Northland in recent decades. Removal of undergrowth by livestock on islands inhibits its presence. Will use logged forest, but in lower densities than in unlogged areas. Major predators of this species are feral cats (Felis catus), black rats and common brushtail possum (Trichosurus vulpecula); control measures have increased breeding success, but there is some poisoning of this petroicid by bait intended for predators and, secondarily, by poisoned invertebrates. Readily adopts nestboxes erected in native forest. Race chathamensis is listed as Endangered nationally and is confined to Chatham Islands EBA; it became extinct on main island of Chatham in 1970s, while an estimated 770–900 individuals were thought to survive in 2001, and an active conservation programme is in place, including translocation efforts (of which just two of seven such efforts have been successful to date). Race marrineri listed as Naturally Uncommon on New Zealand Red List, although there are no estimates of overall numbers, and it is confined to Auckland Islands EBA.

Tomtit (Snares Is.)

VULNERABLE. Global population is put at 250–999 mature individuals, and this species’ population density seems to have remained stable since the middle of the 20th century. Confined to the Snares Is, where it inhabits scrubby tussock grassland, this petroicid has a tiny potential area of occupancy, no more than 3.5 km², and is “naturally uncommon” (15). Any arrival on the islands of non-native mammalian predators could easily have a devastating effect on its numbers, resulting in its rapid extinction. Monitoring of the tomtit’s population, combined with awareness of the potential dangers of invasive species and, if necessary, the implementation of prevention tactics, would appear to be vital.

Distribution of the Tomtit - Range Map
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Distribution of the Tomtit
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Data provided by eBird

Tomtit

Petroica macrocephala

Abundance

Estimates of relative abundance for every week of the year animated to show movement patterns. Relative abundance is the estimated average count of individuals detected by an eBirder during a 1 hour, 1 kilometer traveling checklist at the optimal time of day for each species.   Learn more about this data

Relative abundance
0.66
1.6
2.9
Week of the year
Tomtit, Abundance map
The Cornell Lab logo
Data provided by eBird

Tomtit

Petroica macrocephala

Abundance

Relative abundance is depicted for each season along a color gradient from a light color indicating lower relative abundance to a dark color indicating a higher relative abundance. Relative abundance is the estimated average count of individuals detected by an eBirder during a 1 hour, 1 kilometer traveling checklist at the optimal time of day for each species.   Learn more about this data

Relative abundance
Year-round
0.49
1.8
3.7

Recommended Citation

Boles, W., J. del Hoyo, D. A. Christie, N. Collar, and G. M. Kirwan (2020). Tomtit (Petroica macrocephala), version 1.0. In Birds of the World (S. M. Billerman, B. K. Keeney, P. G. Rodewald, and T. S. Schulenberg, Editors). Cornell Lab of Ornithology, Ithaca, NY, USA. https://doi.org/10.2173/bow.tomtit1.01
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