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Dacrycarpus dacrydioides

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"Kahikatea" redirects here. For Kahikatea statistical area, see Frankton, Hamilton § Demographics.

Kahikatea
Mature kahikatea tree
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Gymnospermae
Division: Pinophyta
Class: Pinopsida
Order: Araucariales
Family: Podocarpaceae
Genus: Dacrycarpus
Species:
D. dacrydioides
Binomial name
Dacrycarpus dacrydioides
Natural range of D. dacrydioides
Synonyms[2]
Alphabetical list
  • Podocarpus dacrydioides A.Rich.
  • Dacrycarpus excelsum D.Don in Lamb.
  • Podocarpus thujoides R.Br. In Bennett
  • Dacrycarpus thuioides Banks et Solander ex Carr.
  • Dacrycarpus ferrugineum Houttee ex Gord.
  • Nageia dacrydioides
  • Nageia excelsa Kuntze
  • Podocarpus excelsus (D. Don.) Druce

Dacrycarpus dacrydioides, commonly known as kahikatea (from Māori) and white pine, is a coniferous tree endemic to New Zealand. A podocarp, it is New Zealand's tallest tree, gaining heights of 60 m over a life span of 600 years. It was first described botanically by the French botanist Achille Richard in 1832 as Podocarpus dacrydioides, and was given its current binomial name Dacrycarpus dacrydioides in 1969 by the American botanist David de Laubenfels. Analysis of DNA has confirmed its evolutionary relationship with other species in the genera Dacrycarpus and Dacrydium.

In Māori culture, it is an important source of timber for the building of waka and making of tools, of food in the form of its berries, and of dye. Its use for timber and its damp fertile habitat, ideal for dairy farming, have led to its decimation almost everywhere except South Westland.

Kahikatea seeds have fleshy structures called receptacles attached to them, which encourage birds such as kererū and tūī to eat them and disperse the seeds. The water storage ability of these structures may also act to protect seeds from drying out. It supports many smaller plants in its own branches, which are called epiphytes; 100 different species have been recorded on one tree alone.

Description

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Kahikatea is a coniferous tree reaching a height of 50–65 m (164–213 ft), making it the tallest New Zealand tree,[3] with a trunk 1–2 m (3.3–6.6 ft) through. It has a 600 year life span and gains maturity after between 250 and 450 years.[4] Near the base of the tree, the roots are typically buttressed and grooved. Adult trees that grow in clusters develop interlocking root islands that may help prevents individual trees from falling during high winds.[5] The wood itself is odourless and white. The majority of the trunk is branchless—in adults around three quarters—and has grey or dark grey coloured bark which falls off thickly in flakes. Young adults have no branches in a third to a half of the trunk and have a conic shape.[2]

In juveniles the leaves are 3–7 (reaching 4 mm in young adults) by 0.5–1 mm and a dark green to red colour that come to a marked point. They are narrow, arranged in almost opposite pairs spreading away from a wider base, and curved like a scythe. In adulthood the leaves change dramatically and are a brown-green colour and just 1–2 mm long, waxy, and grow overlapping one another tightly.[2]

As a conifer, kahikatea has no flowers and instead has cones. Male cones, which occur on different trees to female ones, are 1 cm long and rectangular. The pollen is a pale yellow colour and has a three-pored or trisaccate shape that is distinctive in the New Zealand flora and so can be identified easily.[6] The fruit is highly modified with a yellow-orange fleshy receptacle that is 2.5–6.5 mm long. The purple-black seed is roughly spherical and 4–6 mm in diameter. Both the seed and the ovary are covered with a thin layer of wax.[2] Kahikatea has a diploid chromosome count of 20.[2][7]

  • Male cones with pollen
    Male cones with pollen
  • Female cones beginning to fruit
    Female cones beginning to fruit
  • Ripe fruit
    Ripe fruit
  • Young adult's conical growth habit
    Young adult's conical growth habit

Phytochemistry

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Several different glycosides have been isolated from the leaves; the tricetin 3’,5’-di-O-/β-glucopyranoside and 3’-0-β-xylopyranoside have been found only in kahikatea.[8] The receptacles and seeds have been found to contain anthocyanins, rare in gymnosperms, which it was suggested in one 1988 paper make the fruit as a whole more attractive to prospective animal dispersers.[9]

Taxonomy

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A stand of kahikatea in the Pohangina Valley.

The banks were completely clothed with the finest timber my eyes ever beheld, of a tree we had before seen, but only at a distance [...]. Thick woods of it were everywhere upon the banks, every tree as straight as a pine, and of immense size, and the higher we went the more numerous they were.

— Joseph Banks, possibly describing a former stand on the Waihou River, 1769[10]

Kahikatea was first described in 1832 by the French botanist Achille Richard in his Essai d'une Flore de la Nouvelle Zélande (Essay On The Flora of New Zealand) as Podocarpus dacrydioides.[11][12] There is an earlier record given in the 1825 issue of Mémoires du Muséum d'histoire naturelle as Podocarpus thujoides, but it lacks a description.[13] It was superfluously named Dacrydium excelsum by Allan Cunningham in the 1838 issue of Annals of Natural History,[14] and transferred to the genus Nageia by Otto Kuntze in 1891.[15] It was given its current binomial name, Dacrycarpus dacrydioides, in 1969 by American botanist David de Laubenfels.[12]

Etymology

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Dacrycarpus means tear shaped fruit, and the specific epithet dacrydioides is after its similarity to species in the genus Dacrydium.[2] Common names include kahikatea, from the Māori language, and white pine. Other Māori names recorded by 19th century ethnographers include: katea, kaikatea, koroī, kōaka, kahika, and the name kāī (for the young tree).[16]

Evolution

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A 2022 study in Molecular Phylogenetics and Evolution, found a phylogeny, or evolutionary tree, in which kahikatea is found to be within a Darcydioid clade. This group of species that share a common ancestor also gave rise to the other Dacrycarpus species as well as those in the genus Dacrydium. They suggested it diverged from a common ancestor around 60 million years ago, in the early paleogene.[17] This is represented in the cladogram below.

Distribution and habitat

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Kahikatea in Lake Brunner
The kahikatea can support many other plants, such as those seen here up the trunk and in the higher branches.

Kahikatea is endemic to the North, South, and Stewart Islands of New Zealand. It inhabits mostly lowland forests between 0 and 600m above sea level, though may in rare cases reach montane areas. It used to dominate a swamp forest type that now exists almost only on the South Westland region of the South Island.[2][18] Kahikatea prefers flooded or alluvial soils with low levels of drainage,[2] which in Westland occur from post glaciation events.[19]

Ecology

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Dispersal

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Under optimal circumstances a mature kahikatea can produce 800 kilograms (1,800 lb) of fruit, equivalent to 4.5 million seeds, in a year. The fruit contains a special fleshy structure called a receptacle which helps attract birds such as the kererū, tūī, and bellbird, who then eat the fruit and disperse the seed elsewhere. One 2008 study in the New Zealand Journal of Ecology found a mean retention time of kahikatea seeds in kererū of 44.5 minutes.[20] It was suggested in a 1989 study that the high water content of the receptacle may also help protect the seeds, which are vulnerable to drying out, from dry conditions. It may also serve as a storage vessel for water.[4] The bluish seeds have very strong UV reflectance, which is visible to some species of birds.[21]

Epiphytes

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Kahikatea can support a vast number of non-parasitic plants that live in its branches, called epiphytes. One 2002 study identified between 90 and 100 species occurring on one mature tree. This included 49 vascular plants and over 50 non-vascular plants, which the authors identified as comparable to the number found on a Prumnopitys exigua in Bolivian cloud forest.[22]

Competition

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Intraspecific competition between kahikatea trees was found in a 1999 study to be an important factor in their survival and overall success, affecting both the rates of growth and of mortality. Older trees have a particularly large advantage over resources compared to newer ones, and also have higher growth rates.[23] Following flooding or other natural events, kahikatea has been found to require an open canopy in order to re-establish. Because of the consistency of these events in South Westland however, many forested areas don't progress beyond regaining kahikatea and rimu, as other species, such as kāmahi, need the environment to improve before they can return.[24]

Pests and diseases

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This species plays host to the New Zealand endemic beetle Agapanthida pulchella.[25]

Conservation

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The Palmerston Cooperage and Box Factory was one of many factories used to produce boxes from kahikatea wood.

Prior to the arrival of humans in New Zealand around 75% of the country was covered in trees,[26] and kahikatea dominated its own and once widespread kahikatea forest type. Even after the burning of many forests by early Māori, there still remained large remnant forests which European settlers came upon in the 18th and 19th centuries. Prospects for use as timber were accelerated by the vast numbers of straight and tall trees, but because the wood is soft and odourless, it was made into pulp, barrels and boxes–butter boxes in particular were made mostly out of kahikatea.[27][28] Kahikatea's usually flat habitat, with its damp and fertile soil, was also a prime location for dairy farming. Together this led to the felling of much of the remaining forests in the North and South Islands during the late 19th and early 20th centuries.[2] Today they are confined mostly to the South Westland region of the South Island, though small remnants still exist in some places.[19][29]

Conservation efforts have focused on protecting and fencing kahikatea forests around the country.[30] Riccarton Bush is one notable example of forest remnant protection. The near 16-acre (6.47 ha) reserve was held in the Deans family for 70 years before it was gifted to Christchurch by them in 1914,[31] and subsequently formally protected in the Riccarton Bush Bill.[32] It is the only surviving kahikatea forest remnant in the entire Canterbury Plains, and contains trees up to 600 years old.[33] Reservation of stands may not totally protect kahikatea, however, because the alluvial plains that they favour are prone to upheaval and erosion and so trees may still become damaged.[19] Forest remnants outside of South Westland face the threat of never returning to their natural states, as a result of their small size, threats from weed species, and grazing by livestock.[34] Despite this, kahikatea has been classified as least concern by the International Union for Conservation of Nature and "Not Threatened" by the New Zealand Threat Classification System, which gives it an estimated population of above 100,000.[35][36]

The Whangamarino Wetland, a swamp-fen-bog complex south of Auckland on the North Island, was identified as an area of priority restoration as an ecosystem; the wetland is connected to the Waikato Tainui iwi.[5]

Threats

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The introduced grey willow and crack willow have thrived in the deforested areas where kahikatea was previously dominant. The willows are fast-growing and have obstructed streams, displaced native vegetation, and contributed to a loss in native biodiversity.[5] Kahikatea are considered a light-demanding species that struggles to progress beyond the sapling stage in areas with high willow density. Although the herbicide glyphosate has been successful in thinning mature grey willow canopies and providing a window for reestablishing native sedges, treated willows can rapidly reestablish their populations in an area due to epicormic shoots. Exclusive use of glyphosate to control willow populations would require periodic herbicide application into perpetuity.[5]

The trees are also threatened by diminished seed availability and distribution due to a reduction in native bird species that dispersed the seeds, such as the kererū. Although some non-native birds, such as the common blackbird, are also prolific seed-spreaders, survival of the kahikatea seeds are further threatened by introduced mice and rats.[5]

In Māori culture

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He toa piki rākau kahikatea, he kai na te pakiaka

The champion kahikatea climber is food for the roots

—Māori proverb or Whakataukī that illustrates the dangers of gathering the fruit, [37]

In Māori mythology kahikatea is a child of Tāne, the god of forests and birds, and Hine-wao-riki. It served as an important source of wood for the making of tools, of dye, and of food from its berries. To collect the latter, Māori had to climb sometimes more than 100 ft (30 m) to reach them.[27]

19th century British ethnographers Richard Taylor, Eldson Best, and William Colenso all recorded the fruit of kahikatea being eaten, and that it was given its own name: koroī.[38][39] Best described berries being collected in a basket and then hoisted down using a cord.[40] J. H. Kerry-Nicholls and William Colenso both recorded a blue or black dye being obtained from the soot of burning kahikatea's resin or heart wood, called kāpara or māpara.[40] This was described as then being used in tattooing.[41][42] This resin was also used as chewing gum.[39]

The wood could be made into canoes, called waka, but Best recorded that because of the softness of the wood they were far inferior to those made from tōtara.[40] The heartwood was far stronger and R. H. Matthews described it as being used in tools and weapons such as spears.[43] Medicinal applications were described by W. H. Goldie, who recorded the leaves being used to cure "internal complaints" as a decoction or in a steam bath.[44]

References

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  1. ^ Thomas, P. (2013). "Dacrycarpus dacrydioides". IUCN Red List of Threatened Species. 2013: e.T42443A2980535. doi:10.2305/IUCN.UK.2013-1.RLTS.T42443A2980535.en. Retrieved 19 November 2021.
  2. ^ a b c d e f g h i de Lange, P. J. (2004). "Dacrycarpus dacrydioides". New Zealand Plant Conservation Network. Retrieved 2022-02-12.
  3. ^ Benson, Nigel (23 Jan 2014). "NZ's tallest tree growing ever taller". New Zealand Herald. Retrieved 2022-02-20.
  4. ^ a b Fountain, David W.; Holdsworth, Jacqueline M.; Outred, Heather A. (1989). "The dispersal unit of Dacrycarpus dacrydioides (A. Rich.) de Laubenfels (Podocarpaceae) and the significance of the fleshy receptacle". Botanical Journal of the Linnean Society. 99 (3): 197–207. doi:10.1111/j.1095-8339.1989.tb00399.x. ISSN 0024-4074.
  5. ^ a b c d e Sukias, James P. S.; Tanner, Chris C.; Clarkson, Beverley R.; Bodmin, Kerry A.; Woodward, Simon; Bartlam, Scott; Costley, Kerry (January 2024). "Jump‐starting podocarp forest establishment in a wetland dominated by invasive willow". Restoration Ecology. 32 (1). doi:10.1111/rec.14031. ISSN 1061-2971.
  6. ^ Pocknall, D.T. (1981). "Pollen morphology of the New Zealand species of Dacrydium Selander, Podocarpus L'Heritier, and Dacrycarpus Endlicher (Podocarpaceae)". New Zealand Journal of Botany. 19 (1): 67–95. doi:10.1080/0028825x.1981.10425191. ISSN 0028-825X.
  7. ^ Davies, B. J.; O'Brien, I. E. W.; Murray, B. G. (1997). "Karyotypes, chromosome bands and genome size variation in New Zealand endemic gymnosperms". Plant Systematics and Evolution. 208 (3): 169–185. doi:10.1007/BF00985440. ISSN 1615-6110. S2CID 5624551.
  8. ^ Markham, Kenneth R.; Whitehouse, Lynley A. (1984). "Unique flavonoid glycosides from the new zealand white pine, Dacrycarpus dacrydioides". Phytochemistry. 23 (9): 1931–1936. Bibcode:1984PChem..23.1931M. doi:10.1016/S0031-9422(00)84944-4. ISSN 0031-9422.
  9. ^ Andersen, Øyvind M. (1988). "Semipreparative Isolation and Structure Determination of Pelargonidin 3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside and Other Anthocyanins from the Tree Dacrycarpus dacrydioides". Acta Chemica Scandinavica. 42b: 462–468. doi:10.3891/acta.chem.scand.42b-0462. ISSN 0904-213X.
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  15. ^ Kuntze, Otto (1891). Revisio generum plantarum. Leipzig: A. Felix [etc.] – via the Biodiversity Heritage Library.
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  17. ^ Chen, Luo; Jin, Wei-Tao; Liu, Xin-Quan; Wang, Xiao-Quan (2022-01-01). "New insights into the phylogeny and evolution of Podocarpaceae inferred from transcriptomic data". Molecular Phylogenetics and Evolution. 166: 107341. doi:10.1016/j.ympev.2021.107341. ISSN 1055-7903. PMID 34740782. S2CID 243482772.
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  20. ^ Wotton, Debra M.; Clout, Mick N.; Kelly, Dave (2008). "Seed retention times in the New Zealand pigeon (Hemiphaga novaezeelandiae novaeseelandiae)". New Zealand Journal of Ecology. 32 (1): 1–6. ISSN 0110-6465. JSTOR 24058095.
  21. ^ Lee, W.G.; Hodgkinson, I.J.; Johnson, P.N. (1990-01-01). "A test for ultraviolet reflectance from fleshy fruits of New Zealand plant species". New Zealand Journal of Botany. 28 (1): 21–24. doi:10.1080/0028825X.1990.10412340. ISSN 0028-825X.
  22. ^ Hofstede, Robert G. M.; Dickinson, Katharine J. M.; Mark, Alan F. (2002). "Distribution, abundance and biomass of epiphyte-lianoid communities in a New Zealand lowland Nothofagus-podocarp temperate rain forest: tropical comparisons: Epiphytic-lianoid communities in temperate rainforest". Journal of Biogeography. 28 (8): 1033–1049. doi:10.1046/j.1365-2699.2001.00613.x. S2CID 85726530.
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  24. ^ Duncan, Richard P. (1993). "Flood Disturbance and the Coexistence of Species in a Lowland Podocarp Forest, South Westland, New Zealand". Journal of Ecology. 81 (3): 403–416. doi:10.2307/2261519. ISSN 0022-0477. JSTOR 2261519.
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  28. ^ Wassilieff, Maggy. "Rimu and kahikatea". Te Ara. Retrieved 2022-07-02.
  29. ^ Department of Conservation. "Podocarp-hardwood forests". www.doc.govt.nz. Retrieved 2022-07-02.
  30. ^ Hadden, Peter (2014). North New Zealand. Wairau Press. p. 229. ISBN 9781927158319 – via the Internet Archive.
  31. ^ Wigram, Henry F. (1916). The story of Christchurch, New Zealand. Christchurch: The Lyttleton Times Co., Ltd. pp. 39–40 – via the Internet Archive.
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  33. ^ Fletcher, Jack (2018-09-13). "Riccarton Bush a precious remnant of Canterbury's ecological past". Stuff. Retrieved 2022-07-19.
  34. ^ Smale, Mark C.; Ross, Craig W.; Arnold, Gregory C. (2005). "Vegetation recovery in rural kahikatea (Dacrycarpus dacrydioides) forest fragments in the Waikato region, New Zealand, following retirement from grazing" (PDF). New Zealand Journal of Ecology. 29 (2): 261–269. ISSN 0110-6465.
  35. ^ Thomas, P. (2013). "Dacrycarpus dacrydioides". IUCN Red List of Threatened Species. 2013: e.T42443A2980535. doi:10.2305/IUCN.UK.2013-1.RLTS.T42443A2980535.en. Retrieved 19 November 2021.
  36. ^ "Assessment Details for Dacrycarpus dacrydioides (A.Rich.) de Laub". New Zealand Threat Classification System. Retrieved 2 July 2022.
  37. ^ Park, Geoff (1995). Ngā Uruora. New Zealand: Victoria University Press. p. 35. ISBN 0864732910.
  38. ^ Colenso, William (1868). "Essay on the Botany, Geographic and Economic, of the North Island of the New Zealand Group". Transactions and Proceedings of the Royal Society of New Zealand. 1: 31 – via Papers Past.
  39. ^ a b Taylor, Richard (1855). Te ika a maui, or New Zealand, and its inhabitants. Wertheim and Macintosh – via the Internet Archive.
  40. ^ a b c Eldson, Best (1907). "Maori Forest Lore: being some Account of Native Forest Lore and Woodcraft, as also of many Myths, Rites, Customs, and Superstitions connected with the Flora and Fauna of the Tuhoe or Ure-wera District.—Part I." Transactions and Proceedings of the Royal Society of New Zealand. 40: 180–200 – via Papers Past.
  41. ^ Kerry-Nicholls, J. H. (1886). "The Origin, Physical Characteristics, and Manners and Customs of the Maori Race, from Data Derived During a Recent Exploration of the King Country, New Zealand". The Journal of the Anthropological Institute of Great Britain and Ireland. 15: 187–209. doi:10.2307/2841577. ISSN 0959-5295. JSTOR 2841577.
  42. ^ Colenso, William (1891). "Art. XLVII.—Vestiges: Reminiscences: Memorabilia of Works, Deeds, and Sayings of the Ancient Maoris". Transactions and Proceedings of the Royal Society of New Zealand. 24: 449 – via Papers Past.
  43. ^ Matthews, R. H. (1910). "Reminiscences of Maori life fifty years ago". Transactions of the New Zealand Institute. 43: 598–605 – via Papers Past.
  44. ^ Goldie, W. H. (1904). "Art. I.—Maori Medical Lore: Notes on the Causes of Disease and Treatment of the Sick among the Maori People of New Zealand, as believed and practised in Former Times, together with some Account of Various Ancient Rites connected with the Same". Transactions and Proceedings of the Royal Society of New Zealand. 37: 1–20 – via Papers Past.
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