New Zealand parrot

The New Zealand parrot family, Strigopidae,[1] consists of at least three genera of parrots – Nestor, Strigops, the fossil Nelepsittacus,[2][3] and probably the fossil Heracles.[4] The genus Nestor consists of the kea, kākā, Norfolk kākā and Chatham kākā,[5][6] while the genus Strigops contains the iconic kākāpō.[5] All extant species are endemic to New Zealand.[7] The species of the genus Nelepsittacus were endemics of the main islands, while the two extinct species of the genus Nestor were found at the nearby oceanic islands such as Chatham Island of New Zealand, and Norfolk Island and adjacent Phillip Island.

For the native and introduced parrots of New Zealand in general, see Parrots of New Zealand.

New Zealand parrots
Temporal range: Early Miocene to present
Kākā, North Island subspecies
(Nestor meridionalis septentrionalis)
at Auckland Zoo, New Zealand
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Class: Aves
Order: Psittaciformes
Superfamily: Strigopoidea
Bonaparte, 1849
Family: Strigopidae
Bonaparte, 1849
Genera
Synonyms
  • Nestoridae Bonaparte, 1849

The Norfolk kaka and the Chatham kaka have become extinct in recent times,[8][9] while the species of the genus Nelepsittacus have been extinct for 16 million years. All extant species, the kākāpō, kea, and the two subspecies of the kākā, are threatened.[10][11][12] Human activity caused the two extinctions and the decline of the other three species. Settlers introduced invasive species, such as pigs, cats, foxes, weasels, rats and possums, which eat the eggs of ground-nesting birds, and additional declines have been caused by hunting for food, killing as agricultural pests, habitat loss, and introduced wasps.[13][14][15]

The family diverged from the other parrots around 82 million years ago when New Zealand broke off from Gondwana, while the ancestors of the genera Nestor and Strigops diverged from each other between 60 and 80 million years ago.[16][17]

Systematics

No consensus existed regarding the taxonomy of Psittaciformes until recently. The placement of the Strigopoidea species has been variable in the past.[18] The family belongs to its own superfamily Strigopoidea. This superfamily is one of three superfamilies in the order Psittaciformes; the other two families are Cacatuoidea (cockatoos) and Psittacoidea (true parrots).[19] While some taxonomists include three genera (Nestor, Nelepsittacus, and Strigops) in the family Strigopidae, others place Nestor and Nelepsittacus in the Nestoridae and retain only Strigops in the Strigopidae.[19][20] Traditionally, the species of the family Strigopoidea were placed in the superfamily Psittacoidea, but several studies confirmed the unique placement of this group at the base of the parrot tree.[16][19][21][22]

Phylogeography

An unproven hypothesis for the phylogeography of this group has been proposed, providing an example of various speciation mechanisms at work. In this scenario, ancestors of this group became isolated from the remaining parrots when New Zealand broke away from Gondwana about 82 million years ago, resulting in a physical separation of the two groups.[16][17] This mechanism is called allopatric speciation. Over time, ancestors of the two surviving genera, Nestor and Strigops, adapted to different ecological niches. This led to reproductive isolation, an example of ecological speciation.[17] In the Pliocene, supposedly around five million years ago, the formation of the Southern Alps / Kā Tiritiri o te Moana diversified the landscape and provided new opportunities for speciation within the genus Nestor. Around three million years ago, two lineages may have adapted to high altitude and low altitude, respectively. The high-altitude lineage gave rise to the modern kea, while the low-altitude lineage gave rise to the various kākā species.[17] Island species diverge rapidly from mainland species once a few vagrants arrive at a suitable island. Both the Norfolk kākā and the Chatham kākā are the result of migration of a limited number of individuals to islands and subsequent adaptation to the habitat of those islands.[17] The lack of DNA material for the Chatham kākā makes it difficult to establish precisely when those speciation events occurred. Finally, in recent times, the kākā populations at the North Island and South Island became isolated from each other due to the rise in sea levels when the continental glaciers melted at the end of the Pleistocene.[17]

Until modern times, New Zealand and the surrounding islands were not inhabited by four-legged mammals, an environment that enabled some birds to make nests on the ground and others to be flightless without fear of predation.

The parakeet species belonging to the genus Cyanoramphus (kākāriki) belong to the true parrot family Psittacidae and are closely related to the endemic genus Eunymphicus from New Caledonia. They may have reached New Zealand between 450,000 and 625,000 years ago from mainland Australia by way of New Caledonia, but this is disputed.[23]

Species

Very little is known about the Chatham kākā. The genus Nelepsittacus consists of three described and one undescribed species recovered from early Miocene deposits in Otago.[24] The genus Heracles consists of a giant species also described from the early Miocene of Otago.[25]

Common name
(binomial name)
Status		 Image Description Range and habitat
Nestor
Kea

(Nestor notabilis)
Endangered[12]
48 cm (19 in) long. Mostly olive-green with scarlet underwings and rump. Dark-edged feathers. Dark brown beak, iris, legs, and feet. Male has longer bill.[26] New Zealand: South Island

High-level forests and subalpine scrublands 850–1400 m AMSL.[27]
South Island kākā

(Nestor meridionalis meridionalis)
Endangered[11]
Similar to the North Island kākā, but slightly smaller, brighter colours, the crown is almost white, and the bill is longer and more arched in males.[28] New Zealand: South Island

Unbroken tracts of Nothofagus and Podocarpus forests 450–850 m AMSL in summer and 0–550 m in winter.[27]
North Island kākā

(Nestor meridionalis septentrionalis)
Endangered[11]
About 45 cm (18 in) long. Mainly olive-brown with dark feather edges. Crimson underwings, rump, and collar. The cheeks are golden/brown. The crown is greyish.[28] New Zealand: North Island

Unbroken tracts of Nothofagus and Podocarpus forests between 450 and 850 m AMSL in summer and 0–550 m in winter.[27]
Norfolk kākā

(Nestor productus)
Extinct by 1851 approx.[9]
About 38 cm long. Mostly olive-brown upperparts, (reddish-)orange cheeks and throat, straw-coloured breast, thighs, rump and lower abdomen dark orange.[5] Formerly endemic on Norfolk Island and adjacent Phillip Island[29]

Rocks and trees[5]
Chatham kākā

(Nestor chathamensis)
Extinct by 1500–1650[8]
Only known from subfossil bones.[8] Formerly endemic on Chatham Island of New Zealand

Forests[8]
Strigops
Kākāpō

(Strigops habroptila)
Critically endangered[10]
Large rotund parrots 58–64 cm (23–25 in) long; males are larger than females and weigh 2–4 kg (4.4–8.8 lb) at maturity. Mostly green with brown and yellow mottled barring, the underparts are greenish-yellow. Its face is pale and owl-like.[30] New Zealand: Maud, Chalky, Codfish / Whenua Hou and Anchor Islands
 
Climax Nothofagus (beech) and Podocarpus (conifer) forests, regenerating subalpine scrub, snow tussock Danthonia grassland 10–1400 m AMSL.[27]

Common names
Current distribution of extant species, as well as previous distribution of extinct island species.[27]

All common names for species in this family are the same as the traditional Māori names.[31] The Māori word kākā derives from the ancient Proto-Polynesian word meaning parrot.[32] Kākāpō is a logical extension of that name, as pō means night, resulting in kākā of the night or night parrot, reflecting the species' nocturnal behaviour.[33] (In modern orthography of the Māori language, the long versions of the vowels a and o are written with macrons; i.e., ā and ō. Note that a long ā in Maori should be pronounced like the a in English "father".[34][35] The etymology of kea in Māori is less clear; it might be onomatopoeic of its kee-aah call.[5][36]

Ecology
Kea are well adapted to life in the alpine zone, like these in the Southern Alps. The highest mountain in New Zealand, Aoraki / Mount Cook, is in the background.

The isolated location of New Zealand has made it difficult for mammals to reach the island. This is reflected in the absence of land mammals other than bats. The main predators were birds: harriers, falcons, owls, and the massive, extinct Haast's eagle. Many of the adaptations found in the avifauna reflect the unique context in which they evolved. This unique balance was disrupted with the arrival of the Polynesians, who introduced the Polynesian rat and the kurī (Polynesian dog) to the island. Later, Europeans introduced many more species, including large herbivores and mammalian predators.

The three extant species of this family occupy rather different ecological niches, a result of the phylogeographical dynamics of this family. The kākāpō is a flightless, nocturnal species, well camouflaged to avoid the large diurnal birds of prey on the island, while the local owls are too small to prey on the kākāpō at night. The kākāpō is the only flightless bird in the world to use a lek-breeding system. Usually, they breed only every 3–5 years when certain podocarp trees like rimu (Dacrydium cupressinum) mast abundantly.

The kea is well adapted to life at high altitudes, and they are regularly observed in the snow at ski resorts. As trees are absent in the alpine zone, they breed in hollows in the ground instead of in tree hollows like most parrot species.

Relationship with humans

Importance to the Māori

The parrots were important to the Māori in various ways. They hunted them for food, kept them as pets, and used their feathers in weaving[37] such items as their kahu huruhuru (feather cloak).[38] Feathers were also used to decorate the head of the taiaha, a Māori weapon, but were removed prior to battle.[39] The skins of the kākāpō with the feathers attached were used to make cloaks (kākahu) and dress capes (kahu kākāpō), especially for the wives and daughters of chiefs.[39] Māori like to refer to the kākā in the tauparapara, the incantation to begin their mihi (tribute), because their voice (reo) is continuous.[40][41]

Status

Of the five species, the Norfolk kākā[9][29] and Chatham kākā[8] became extinct in recent history. The last known Norfolk kākā died in captivity in London sometime after 1851,[42] and only between seven[43] and 20[44] skins survive. The Chatham kākā became extinct between 1500 and 1650 in pre-European times, after Polynesians arrived at the island, and is only known from subfossil bones.[8] Of the surviving species, the kākāpō is critically endangered,[10][30] with living individuals numbering only 247 as of 2023.[45] The mainland kākā is listed as endangered,[11][28] alongside the kea.

Threats

The fauna of New Zealand evolved in the total absence of humans and other mammals. Only a few bat species and sea mammals were present prior to colonisation by humans, and the only predators were birds of prey that hunt by sight. These circumstances influence the design of New Zealand's parrots, for example, the flightlessness of the kākāpō and the ground breeding of the kea.[39] Polynesians arrived at Aotearoa between 800 and 1300 AD,[46] and introduced the kurī (dog) and kiore (Polynesian rat) to the islands.[39][47] This was disastrous for the native fauna, because mammalian predators can locate prey by scent, and the native fauna had no defence against them.[39]

The kākāpō was hunted for its meat, skin, and plumage. When the first European settlers arrived, the kākāpō was already declining, but still widespread.[39] The large-scale clearance of forests and bush destroyed its habitat while introduced predators such as rats, cats, and stoats found the flightless, ground-nesting birds easy prey.

The New Zealand kākā needs large tracts of forest to thrive, and the continued fragmentation of forests due to agriculture and logging has a devastating effect on this species. Another threat comes from competition with introduced species for food, for example with possums for the endemic mistletoe and rata and with wasps for shimmering honeydew, an excretion of scale insects. Females, young, and eggs are particularly vulnerable in the tree hollows in which they nest.

The kea nests in holes in the ground, again making it vulnerable to introduced predators. Another major threat, resulting from development of the alpine zone, is their opportunistic reliance on human food sources as their natural food sources dwindle.[15]

Conservation

Recovery programs for the kākāpō and the kākā have been established, while the kea is also closely monitored.[48] The 247 as of 2023.[49] living kākāpō are all in a breeding and conservation program. Each one has been individually named.

See also

References
  1. Nestoridae and Strigopidae are described in the same article, Bonaparte, C.L. (1849) Conspectus Systematis Ornithologiae. Therefore, under rules of the ICZN, the first reviser determines priority, which is Bonaparte, C.L. (1850), Conspectus Generum Avium, E.J. Brill, Leyden.
  2. Christidis L, Boles WE (2008). Systematics and Taxonomy of Australian Birds. Canberra: CSIRO Publishing. p. 200. ISBN 978-0-643-06511-6.
  3. Worthy, Trevor H.; Tennyson, Alan J. D.; Scofield, R. Paul (2011). "An early Miocene diversity of parrots (Aves, Strigopidae, Nestorinae) from New Zealand". Journal of Vertebrate Paleontology. 31 (5): 1102–16. doi:10.1080/02724634.2011.595857. S2CID 86361015.
  4. Worthy, Trevor H.; Hand, Suzanne J.; Archer, Michael; Schofield, R. Paul; De Pietri, Vanesa L. (2019). "Evidence for a giant parrot from the early Miocene of New Zealand". Biology Letters. 15 (8): 20190467. doi:10.1098/rsbl.2019.0467. PMC 6731479. PMID 31387471.
  5. Forshaw, Joseph M.; Cooper, William T. (1981) [1973, 1978]. Parrots of the World (corrected second ed.). David & Charles, Newton Abbot, London. ISBN 0-7153-7698-5.
  6. Millener, P. R. (1999). "The history of the Chatham Islands' bird fauna of the last 7000 years – a chronicle of change and extinction. Proceedings of the 4th International meeting of the Society of Avian Paleontology and Evolution (Washington, D.C., June 1996)". Smithsonian Contributions to Paleobiology. 89: 85–109.
  7. Forshaw, Joseph Michael (2017). Vanished and vanishing parrots : profiling extinct and endangered species. Collingwood: CSIRO Publishing. p. 19. ISBN 978-1501704697. Retrieved 17 September 2022.
  8. Millener, P. R. (1999). "The history of the Chatham Islands' bird fauna of the last 7000 years – a chronicle of change and extinction. Proceedings of the 4th International meeting of the Society of Avian Paleontology and Evolution (Washington, D.C., June 1996)". Smithsonian Contributions to Paleobiology. 89: 85–109.
  9. BirdLife International (2016). "Nestor productus". IUCN Red List of Threatened Species. 2016: e.T22684834A93049105. doi:10.2305/IUCN.UK.2016-3.RLTS.T22684834A93049105.en. Retrieved 12 November 2021.
  10. BirdLife International (2018). "Strigops habroptila". IUCN Red List of Threatened Species. 2018: e.T22685245A129751169. doi:10.2305/IUCN.UK.2018-2.RLTS.T22685245A129751169.en. Retrieved 12 November 2021. Database entry includes a range map and justification for why this species is endangered,
  11. BirdLife International (2016). "Nestor meridionalis". IUCN Red List of Threatened Species. 2016: e.T22684840A93049267. doi:10.2305/IUCN.UK.2016-3.RLTS.T22684840A93049267.en. Retrieved 12 November 2021. Database entry includes a range map and justification for why this species is endangered.
  12. BirdLife International (2017). "Nestor notabilis". IUCN Red List of Threatened Species. 2017: e.T22684831A119243358. doi:10.2305/IUCN.UK.2017-3.RLTS.T22684831A119243358.en. Retrieved 12 November 2021. Database entry includes a range map and justification for why this species is endangered.
  13. "Threats to Kākāpō". Department of Conservation Te Papa Atawbai. Archived from the original on 2009-04-04. Retrieved 2008-12-31.
  14. "Threats to Kākā". Department of Conservation Te Papa Atawbai. Archived from the original on 2008-12-31. Retrieved 2008-12-31.
  15. "Threats to Kea". Department of Conservation Te Papa Atawbai. Archived from the original on 2009-10-03. Retrieved 2008-12-31.
  16. Wright, T.F.; Schirtzinger E. E.; Matsumoto T.; Eberhard J. R.; Graves G. R.; Sanchez J. J.; Capelli S.; Muller H.; Scharpegge J.; Chambers G. K.; Fleischer R. C. (2008). "A Multilocus Molecular Phylogeny of the Parrots (Psittaciformes): Support for a Gondwanan Origin during the Cretaceous". Mol Biol Evol. 25 (10): 2141–2156. doi:10.1093/molbev/msn160. PMC 2727385. PMID 18653733.
  17. Grant-Mackie, E.J.; J.A. Grant-Mackie; W.M. Boon; G.K. Chambers (2003). "Evolution of New Zealand Parrots". NZ Science Teacher. 103.
  18. For a discussion about older taxonomic positions, see Sibley, Charles Gald; Jon E. Ahlquist (1991). Phylogeny and Classification of Birds. Yale University Press. For more recent taxonomies, see Christides.
  19. Leo Joseph, Alicia Toon, Erin E. Schirtzinger, Timothy F. Wright & Richard Schodde. (2012) A revised nomenclature and classification for family-group taxa of parrots (Psittaciformes). Zootaxa 3205: 26–40
  20. Homberger, D. G. (2006). "Classification and the status of wild populations of parrots". In Luescher AU (ed.). Manual of parrot behavior. Ames, Iowa: Blackwell Publishing. pp. 3–11. ISBN 978-0-8138-2749-0.
  21. Tokita, M; Kiyoshi T; Armstrong KN (2007). "Evolution of craniofacial novelty in parrots through developmental modularity and heterochrony". Evolution & Development. 9 (6): 590–601. doi:10.1111/j.1525-142X.2007.00199.x. PMID 17976055. S2CID 46659963. Archived from the original on 2012-10-05.
  22. de Kloet, RS; de Kloet SR (2005). "The evolution of the spindlin gene in birds: Sequence analysis of an intron of the spindlin W and Z gene reveals four major divisions of the Psittaciformes". Molecular Phylogenetics and Evolution. 36 (3): 706–721. doi:10.1016/j.ympev.2005.03.013. PMID 16099384.
  23. Boon, W. M.; Kearvell, J.; Daugherty, C. H.; Chambers, G. K. (2001). "Molecular systematics and conservation of kakariki (Cyanoramphus spp.)" (PDF). Science for Conservation. 176.
  24. Worthy, Trevor H.; Tennyson, Alan J. D.; Scofield, R. Paul (2011). "An early Miocene diversity of parrots (Aves, Strigopidae, Nestorinae) from New Zealand". Journal of Vertebrate Paleontology. 31 (5): 1102–16. doi:10.1080/02724634.2011.595857. S2CID 86361015.
  25. Worthy, Trevor H.; Hand, Suzanne J.; Archer, Michael; Schofield, R. Paul; De Pietri, Vanesa L. (2019). "Evidence for a giant parrot from the early Miocene of New Zealand". Biology Letters. 15 (8): 20190467. doi:10.1098/rsbl.2019.0467. PMC 6731479. PMID 31387471.
  26. "Kea – BirdLife Species Factsheet". BirdLife International. 2008.
  27. Juniper, Tony; Mike Parr (1998). Parrots: A Guide to Parrots of the World. Yale University Press. ISBN 978-0300074536.
  28. "Kaka – BirdLife Species Factsheet". BirdLife International. 2008.
  29. "Norfolk Island Kaka – BirdLife Species Factsheet". BirdLife International. 2008.
  30. "Kakapo – BirdLife Species Factsheet". BirdLife International. 2008.
  31. "Maori Bird Names". Kiwi Conservation Club. Archived from the original on 22 May 2010. Retrieved 12 December 2012.
  32. "Kaakaa". Polynesian Lexicon Online. Retrieved 2012-02-29.
  33. "kakapo". The American Heritage Dictionary of the English Language: Fourth Edition. 2000. Archived from the original on 2008-04-20. Retrieved 2008-12-31.
  34. "The Māori Language – Ko Te Reo". Retrieved 2009-01-01.
  35. "Māori dictionary". Retrieved 2009-01-02.
  36. "kea". The American Heritage Dictionary of the English Language: Fourth Edition. 2000. Archived from the original on 2008-04-18. Retrieved 2008-12-31.
  37. Evans, Miriama; Ranui Ngarimu; Creative New Zealand; Norman Heke (2005). The Art of Māori Weaving. Wellington, N.Z.: Huia Publishers. ISBN 978-1-86969-161-5.
  38. "Kahu huruhuru (feather cloak)". Museum of New Zealand Te Papa Tongarewa. Retrieved 2008-12-31.
  39. Tipa, Rob (2006). "Kakapo in Maori lore" (PDF). Notornis. 53: 193–194. Archived from the original (PDF) on 2008-10-14.
  40. "Putting Together a Mihi for a Hui" (PDF). maori.org.nz Main Maori Site on the Net!. Retrieved 2009-01-02.
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  42. Greenway, James Cowan (1967). Extinct and Vanishing Birds of the World (2nd ed.). New York: Dover Publications.
  43. "Nestor productus – Norfolk Island Kaka specimen(s) in the ZMA". Nlbif.eti.uva.nl. Archived from the original on 2011-06-08. Retrieved 2008-12-28.
  44. "Naturalis – Extinct bird: Nestor productus (Norfolk Island Kaka)". Nlbif.eti.uva.nl. Archived from the original on 2011-06-08. Retrieved 2008-12-28.
  45. "Kākāpō Recovery". Department of Conservation. New Zealand. Retrieved 28 August 2023
  46. Douglas G. Sutton, ed. (1994). The Origins of the First New Zealanders. Auckland: Auckland University Press. ISBN 1-86940-098-4.
  47. Tahana, Yvonne (2 June 2010). "Rare rats off the hook as DoC gives them island sanctuary". The New Zealand Herald. Retrieved 17 February 2019.
  48. "DOC's work with Kea". Department of Conservation Te Papa Atawbai. Archived from the original on 2009-10-04. Retrieved 2008-12-31.
  49. "Kākāpō Recovery". Department of Conservation. New Zealand. Retrieved 28 August 2023
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