Araucariaceae

Tāne Mahuta ("Lord of the Forest"), a massive Agathis australis tree from New Zealand

Members of Araucariaceae are typically extremely tall evergreen trees,[2] reaching heights of 60 m (200 ft) or more.[3] They can also grow very large stem diameters; a New Zealand kauri tree (Agathis australis) named Tāne Mahuta ("The Lord of the Forest") has been measured at 45.2 m (148 ft) tall with a diameter at breast height of 491 cm (16.11 ft). Its total wood volume is calculated to be 516.7 m³ (18,250 cu ft),[4] making it the third-largest conifer after Sequoia and Sequoiadendron (both from the Cupressaceae subfamily Sequoioideae).[2]

The trunks are columnar and have relatively large piths with resinous cortices.[5] The branching is usually horizontal and tiered, arising regularly in whorls of three to seven branches or alternating in widely separated pairs.[6]

The leaves can be small, needle-like, and curved, or they can be large, broadly ovate, and flattened.[7] They are spirally arranged, persistent, and usually have parallel venation.[2]

Like other conifers, they produce cones. Each tree can have both male and female cones (monoecious) or they can have only male or female cones (dioecious).[8]

Male cones are among the largest among all conifer cones, on average. They are cylindrical and drooping, somewhat resembling catkins. They are borne singly on the tips of branches or the axils of leaves. They contain numerous sporophylls arranged in whorls or spirals. Each has four to 20 elongated pollen sacs attached to the lower surface at one end. The pollen grains are round and do not possess wings or air sacs.[2][6][7]

Female cones are also very large. They are spherical to ovoid in shape and borne erect on thick, short shoots at branch tips. The numerous bracts and scales are either fused to each other or separate for half of their lengths.[2][6][7] The scales almost always bear only one seed on its upper surface, in contrast to two in true pines (family Pinaceae).[9] They are very large, among the largest seeds among conifers. They are dispersed by wind, usually using wing-like structures. On maturity, the female cones detach and fall to the ground.[2][6][7] Due to their size, they can cause serious injuries if they hit a person. The cones of the bunya bunya, Araucaria bidwillii, for example, weigh up to 10 kg (22 lb),[10] about the size and weight of a large pineapple. They can drop from heights of 23 m (75 ft).[9]

Araucaria heterophylla

Agathis robusta

Wollemia nobilis

Araucariaceae is classified under the order Pinales, class Pinopsida of the division Pinophyta. The division includes all living conifers. Recently however, some authorities treat Araucariaceae as a separate order, Araucariales.[2]

Araucariaceae contains three extant genera and about 41 species.[5]

Image	Genus	Living Species	Distribution
	Araucaria Jussieu	Araucaria angustifolia – Paraná pine Araucaria araucana – monkey-puzzle or pehuén Araucaria bidwillii – bunya-bunya Araucaria hunsteinii – klinki Araucaria bernieri Araucaria biramulata Araucaria columnaris - Cook pine Araucaria cunninghamii - Moreton Bay pine, hoop pine Araucaria goroensis Araucaria heterophylla – Norfolk Island pine Araucaria humboldtensis Araucaria laubenfelsii Araucaria luxurians Araucaria montana Araucaria muelleri Araucaria nemorosa Araucaria rulei Araucaria schmidii Araucaria scopulorum Araucaria subulata	19 living species found in New Caledonia (where 13 species are endemic), Norfolk Island, Australia, New Guinea, Argentina, Chile, and Brazil.
	Agathis Salisbury	Agathis atropurpurea—black kauri, blue kauri (Queensland, Australia) Agathis australis—kauri, New Zealand kauri (North Island, New Zealand) Agathis borneensis (western Malesia, Borneo) Agathis corbassonii—red kauri (New Caledonia) Agathis dammara (syn. A. alba, A. celebica, A. loranthifolia)—Bindang (eastern Malesia) Agathis endertii (Borneo) Agathis flavescens (Peninsular Malaysia) Agathis kinabaluensis (Borneo) Agathis labillardieri (New Guinea) Agathis lanceolata (New Caledonia) Agathis lenticula (Borneo) Agathis macrophylla (syn. A. vitiensis)—Pacific kauri, dakua (Fiji, Vanuatu, Solomon Islands) Agathis microstachya—bull kauri (Queensland, Australia) Agathis montana (New Caledonia) Agathis moorei—white kauri (New Caledonia) Agathis orbicula (Borneo) Agathis ovata (New Caledonia) Agathis philippinensis (Philippines, Sulawesi) Agathis robusta—Queensland kauri (Queensland, Australia; New Guinea) Agathis silbae (Vanuatu) Agathis spathulata—New Guinea kauri (Papua New Guinea) Agathis zamunerae—Patagonia, South America (Argentina)	New Zealand, Australia, Vanuatu, New Caledonia, Papua New Guinea, Indonesia, Malaysia, and the Philippines
	Wollemia W.G. Jones, K.D. Hill & J.M. Allen	Wollemia nobilis	endemic to Australia. It was known only from fossil remains before the discovery of the living species in 1994.

Below is the phylogeny of the Pinophyta based on cladistic analysis of molecular data. It shows the position of Araucariaceae within the division.[11]

Relationships between living members of Araucariaceae.[12]

Molecular evidence supports Araucariaceae and Podocarpaceae having diverged from each other during the late Permian.[13]

Today, 41 species are known, in three genera: Agathis, Araucaria and Wollemia, distributed largely in the Southern Hemisphere.

By far the greatest diversity is in New Caledonia (18 species), with others in Australia, Argentina, New Zealand, Chile, southern Brazil, and Malesia. In Malesia, Agathis extends a short distance into the Northern Hemisphere, reaching 18°N in the Philippines.

Several species are very popular ornamental trees in gardens in subtropical regions, and some are also very important timber trees, producing wood of high quality. Several have edible seeds similar to pine nuts, and others produce valuable resin and amber. In the forests where they occur, they are usually dominant trees, often the largest species in the forest; the largest is Araucaria hunsteinii, reported to 89 m tall in New Guinea, with several other species reaching 50–65 m tall. A. heterophylla, the Norfolk Island pine, is a well-known landscaping and house plant from this taxon.

Skillful artisans in the Erzurum Province, Turkey, have used fossilized wood of Araucariaceae for centuries to manufacture jewelry and decorative items. It is known as "Oltustone", the name deriving from the town of Oltu, where it is most commonly excavated. Despite the fact that this semiprecious gemstone is classified as “stone”, wood anatomy reveals it was fossilized pieces of trunks of Araucariacea. Oltustone, also called ‘Black Amber’ is unique to Turkey. It is dull and black, but when polished, acquires an attractive black sheen.[14]

Fossils widely believed to belong to Araucariaceae include the form genera Araucarites (various), Agathoxylon and Araucarioxylon (wood), Brachyphyllum (leaves), Araucariacites and Dilwynites (pollen), and Protodammara (cones).

The oldest definitive records of Araucariaceae are from the Early Jurassic, though there are potential earlier Late Triassic records. Early representatives of Araucaria are widespread across both hemispheres by the Middle Jurassic, such as Araucaria mirabilis and Araucaria sphaerocarpa from the Middle Jurassic of Argentina and England respectively.[15] The oldest records of the Wollemia-Agathis lineage from the Cretaceous, including Emwadea microcarpa from the Albian aged Winton Formation of Australia[16] and Wairarapaia mildenhallii from the Albian-Cenomanian of New Zealand.[17][12] The oldest fossils currently confidently assignable to Agathis are those of Agathis immortalis from the Salamanca Formation of Patagonia, which dates to the Paleocene, approximately 64.67–63.49 million years ago. Agathis-like leaves are also known from the slightly older Lefipán Formation of the same region, which date to the very end of the Cretaceous.[18]

Wikimedia Commons has media related to Araucariaceae.

Wikispecies has information related to Araucariaceae.

• Paleobotany
• Te Matua Ngahere

• Cookson, I. C.; Duigan, S. L. (1951). "Tertiary Araucariaceae from South-eastern Australia, with notes on living species". Australian Journal of Scientific Research Series B (Biological Sciences). 4: 415–449.
• Kendall, Mabel W (1949). "A Jurassic member of the Araucariaceae". Annals of Botany. New Series. 13 (50): 151–161. doi:10.1093/oxfordjournals.aob.a083211.
• Kershaw, Peter; Wagstaff, Barbara (2001). "The Southern Conifer Family Araucariaceae: History, Status, and Value for Paleoenvironmental Reconstruction". Annual Review of Ecology and Systematics. 32: 397–414. doi:10.1146/annurev.ecolsys.32.081501.114059.
• Krasilov, Valentin A (1978). "Araucariaceae as indicators of climate and paleolatitudes". Review of Palaeobotany and Palynology. 26 (1–4): 113–124. Bibcode:1978RPaPa..26..113K. doi:10.1016/0034-6667(78)90008-8.
• Pye, Matthew G.; Henwood, Murray J.; Gadek, Paul A. (2009). "Differential levels of genetic diversity and divergence among populations of an ancient Australian rainforest conifer, Araucaria cunninghamii". Plant Systematics and Evolution. 277 (3/4): 173–185. doi:10.1007/s00606-008-0120-1. S2CID 21846658.
• Setoguchi, Hiroaki; et al. (1998). "Phylogenetic relationships within Araucariaceae based on rbcL gene sequences". American Journal of Botany. 85 (11): 1507–1516. doi:10.2307/2446478. JSTOR 2446478. PMID 21680310.
• Stockey, Ruth A (1982). "The Araucariaceae: an evolutionary perspective". Review of Palaeobotany and Palynology. 37 (1–2): 133–154. Bibcode:1982RPaPa..37..133S. doi:10.1016/0034-6667(82)90041-0.
• Stockey, Ruth A (1994). "Mesozoic Araucariaceae: morphology and systematic relationships". Journal of Plant Research. 107 (4): 493–502. doi:10.1007/BF02344070. S2CID 20148157.