Nageia
Nageia Temporal range:
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Nageia nagi[3] | |
Scientific classification ![]() | |
Kingdom: | Plantae |
Clade: | Tracheophytes |
Clade: | Gymnospermae |
Division: | Pinophyta |
Class: | Pinopsida |
Order: | Araucariales |
Family: | Podocarpaceae |
Genus: | Nageia Gaertn. 1788 not Roxb. 1832 (syn of Putranjiva in Putranjivaceae)[1] |
Type species | |
Nageia nagi | |
Species | |
See text. |
Nageia is a genus of conifers belonging to the podocarp family Podocarpaceae.[4] Nageia includes evergreen shrubs and trees, from one to 54 meters in height. A 2009 treatment of the genus recognized five species.[5] Some authors consider Nageia formosensis to be a separate species from Nageia nagi, thus recognizing six species. The podocarp genera have been reshuffled by various botanists. Most recently, several species formerly classed as Nageia were moved to the new genus Retrophyllum, while Nageia falcata and Nageia mannii were moved to the new genus Afrocarpus.
Description
[edit]Nageia are evergreen woody plants that usually grow as trees but may also rarely be shrubs, varying in height from one to 54 meters.[6] The branching is irregular.[7] The thin and hard bark often peels with scale-like plates.[7]
The leaves are simple and flat. The phyllotaxis or leaf arrangement can be spiral or subopposite and nearly decussate.[7][8] The leaf petioles are frequently twisted so the leaves form a flat plane around the shoot.[6][7] The leaf blade is elliptic, ovate-elliptic or lanceolate in shape.[6][7] Juvenile leaves are similar in shape to the adult leaves but may be larger or smaller depending on the species.[8] The leaves have multiple parallel longitudinal veins converging toward the ends. Stomata may be found on either both surfaces of the leaf or only the abaxial or underside. The leaf surface is coriaceous.[7]
Nageia are generally dioecious, with male pollen cones and female seed cones borne on separate individual plants but may sometimes be monoecious. The cones are pedunculate and develop from axillary buds.[7][8]
The pollen cones are long and ovoid-cylindric in shape. They may be solitary or grow in small spicate groups of two to six cones.[7][8] Each pollen cone has numerous spirally inserted microsporophylls. The microsprophylls may be triangular or apiculate in shape. Each of them has two basal pollen sacs with bisaccate pollen.[7]
The seed cones are solitary and have long peduncles. They have several sterile and one or rarely two fertile scales, each fertile scale with one seed producing ovule.[7] Depending on the species, as the cone matures, the sterile scales may fuse and become fleshy as in the closely related Podocarpus or they may wither.[7][8] A part of the cone scale supporting the ovule develops into a drupe-like fleshy covering known as the epimatium.[6][7] The fleshy parts of the cones attract birds, which then disperse the seeds in their droppings.[9]
The species of Nageia are distinguished from similar Podocarpus and the other genera in the Podocarpaceae by their broad, flat subopposite leaves with no midrib, superficially similar to those of the unrelated Agathis (Araucariaceae). Nageia is the only genus in Podocarpaceae with multi-veined leaves.
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Broad leaves of N. wallichiana.
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A pair of male cones of N. nagi.
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Female cones of N. nagi with a brown epimatium around the seed.
Distribution
[edit]Nageia can be found in the tropical and subtropical moist broadleaf forests of Asia and Australasia, from Assam in eastern India across Southeast Asia to southern China and southern Japan, and across Malesia, from the Malay Peninsula across Indonesia to New Guinea and New Britain.[2] An outpost of N. wallichiana is found in the South Western Ghats montane rain forests of southern India, where it is thought to be a relatively recent colonist in biogeographical terms.
Nageia, like many podocarps, can usually be found scattered throughout the forest mixed with other trees, and is rarely if ever found growing in pure stands. The wood is yellowish, typical of podocarps, and a few species are locally important for lumber.
The oldest fossils assigned to the genus are known from the Early Cretaceous of Japan, China and Russia. Other fossils are known from the Eocene of China.[10][11]
Classification
[edit]Phylogeny of Nageia[12][13] | |||||||||||||||||||||||||||||||||
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The genus contains six species:[2][7]
Image | Scientific name | Distribution |
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Nageia fleuryi | S China, E Indochina |
Nageia formosensis | Taiwan | |
Nageia maxima | Sarawak | |
Nageia motleyi | S Thailand, W Malaysia, Borneo, Sumatra | |
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Nageia nagi | S China (incl. Hainan), Kyushu in Japan, Taiwan |
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Nageia wallichiana | SW India; widespread from Assam + Yunnan to Maluku |
- formerly included[2]
moved to other genera: Acmopyle Afrocarpus Amentotaxus Cephalotaxus Dacrycarpus Dacrydium Falcatifolium Madhuca Parasitaxus Podocarpus Prumnopitys Putranjiva (Putranjivaceae) Retrophyllum Sundacarpus
- N. acutifolia — Podocarpus acutifolius
- N. affinis — Podocarpus affinis
- N. alpina — Podocarpus lawrencei
- N. amara — Sundacarpus amarus
- N. andina — Prumnopitys andina
- N. angustifolia — Podocarpus parlatorei
- N. appressa — Podocarpus macrophyllus var. maki
- N. argotaenia — Amentotaxus argotaenia
- N. aristulata — Podocarpus angustifolius
- N. beccarii — Dacrydium beccarii
- N. bracteata — Podocarpus bracteatus
- N. chilina — Podocarpus salignus
- N. chinensis — Podocarpus macrophyllus var. maki
- N. comptonii — Retrophyllum comptonii
- N. coriacea — Podocarpus coriaceus
- N. corrugata — Podocarpus macrophyllus var. maki
- N. costalis — Podocarpus costalis
- N. cumingii — Dacrycarpus cumingii
- N. cupressina — Dacrycarpus imbricatus
- N. curvifolia — Prumnopitys montana
- N. dacrydioides — Dacrycarpus dacrydioides
- N. discolor — Podocarpus neriifolius
- N. drouyniana — Podocarpus drouynianus
- N. elata — Podocarpus elatus
- N. elongata — Podocarpus elongatus
- N. endlicheriana — Podocarpus neriifolius
- N. ensifolia — Podocarpus spinulosus
- N. eurhyncha — Sundacarpus amarus
- N. excelsa — Dacrycarpus dacrydioides
- N. falcata — Afrocarpus falcatus
- N. falciformis — Falcatifolium falciforme
- N. ferruginea — Prumnopitys ferruginea
- N. flagelliformis — Podocarpus macrophyllus var. maki
- N. glomerata — Podocarpus glomeratus
- N. gnidioides — Podocarpus gnidioides
- N. hallii — Podocarpus cunninghamii
- N. insignis — Amentotaxus argotaenia
- N. japonica (Siebold ex Endl.) Kuntze 1891 not Gaertn. 1788 - Podocarpus macrophyllus var. maki
- N. kirkiana — Podocarpus acutifolius
- N. koraiana — Cephalotaxus harringtonii
- N. laeta — Podocarpus spinulosus
- N. lambertii — Podocarpus lambertii
- N. latifolia (Thunb.) Kuntze 1891 not Gordon 1858 - Podocarpus latifolius
- N. leptostachya — Podocarpus neriifolius
- N. macrophylla — Podocarpus macrophyllus
- N. macrostachya — Podocarpus oleifolius
- N. madagascariensis — Podocarpus madagascariensis
- N. mannii — Afrocarpus mannii
- N. mannii var. dawei — Afrocarpus dawei
- N. mannii var. usambarensis — Afrocarpus usambarensis
- N. meyeriana — Afrocarpus falcatus
- N. minor — Retrophyllum minus
- N. montana — Prumnopitys montana
- N. neglecta — Podocarpus neriifolius
- N. neriifolia — Podocarpus neriifolius
- N. nivalis — Podocarpus nivalis
- N. novae-caledoniae — Podocarpus novae-caledoniae
- N. nubigena — Podocarpus nubigenus
- N. oleifolia — Podocarpus oleifolius
- N. palembanica — Madhuca palembanica
- N. pancheri — Acmopyle pancheri
- N. parvifolia — Podocarpus lawrencei
- N. piresii — Retrophyllum piresii
- N. polystachya — Podocarpus polystachyus
- N. purdieana — Podocarpus purdieanus
- N. putranjiva — Putranjiva roxburghii
- N. rospigliosii — Retrophyllum rospigliosii
- N. rumphii — Podocarpus rumphii
- N. salicifolia — Podocarpus salicifolius
- N. sellowii — Podocarpus sellowii
- N. spicata — Prumnopitys taxifolia
- N. spinulosa — Podocarpus spinulosus
- N. sprucei — Podocarpus sprucei
- N. taxoides — Falcatifolium taxoides
- N. tenuifolia — Dacrycarpus vieillardii
- N. teysmannii — Podocarpus teysmannii
- N. thevetiifolia — Podocarpus polystachyus
- N. thunbergii — Podocarpus latifolius
- N. totara — Podocarpus totara
- N. usta — Parasitaxus ustus
- N. valdiviana — Prumnopitys andina
- N. vieillardii — Dacrycarpus vieillardii
- N. vitiensis — Retrophyllum vitiense
References
[edit]- ^ Kew World Checklist of Selected Plant Families, Nageia Roxb.
- ^ a b c d Kew World Checklist of Selected Plant Famiiles, Nageia Gaertn.
- ^ illustration from Flora Japonica, Sectio Prima (Tafelband). 1870 by Philipp Franz von Siebold and Joseph Gerhard Zuccarini
- ^ Christopher N. Page. 1990. "Podocarpaceae" pages 332-346. In: Klaus Kubitzki (general editor); Karl U. Kramer and Peter S. Green (volume editors) The Families and Genera of Vascular Plants volume I. Springer-Verlag: Berlin;Heidelberg, Germany. ISBN 978-0-387-51794-0
- ^ James E. Eckenwalder. 2009. Conifers of the World. Timber Press: Portland, OR, USA. ISBN 978-0-88192-974-4.
- ^ a b c d Earle, Christopher J. (2012). "Nageia". The Gymnosperm Database, conifers.org. Retrieved April 2, 2016.
- ^ a b c d e f g h i j k l m Farjon, Aljos (2010). A Handbook of the World's Conifers. Leiden: Brill. p. 518. ISBN 9789004177185.
- ^ a b c d e "Nageia". eFloras: Flora of China. Missouri Botanical Garden, St. Louis, MO & Harvard University Herbaria, Cambridge, MA. 1999. Retrieved April 2, 2016.
- ^ Flora of China Vol. 4 Page 79 竹柏属 zhu bai shu Nageia Gaertner, Fruct. Sem. Pl. 1: 191. 1788.
- ^ Liu, Xiao-Yan; Gao, Qi; Jin, Jian-Hua (July 2015). "Late Eocene leaves of Nageia (section Dammaroideae ) from Maoming Basin, South China and their implications on phytogeography: Late Eocene Nageia section Dammaroideae from South China". Journal of Systematics and Evolution. 53 (4): 297–307. doi:10.1111/jse.12133. S2CID 83810731.
- ^ Andruchow-Colombo, Ana; Escapa, Ignacio H; Aagesen, Lone; Matsunaga, Kelly K S (2023-08-04). "In search of lost time: tracing the fossil diversity of Podocarpaceae through the ages". Botanical Journal of the Linnean Society. 203 (4): 315–336. doi:10.1093/botlinnean/boad027. hdl:11336/227952. ISSN 0024-4074.
- ^ Stull, Gregory W.; Qu, Xiao-Jian; Parins-Fukuchi, Caroline; Yang, Ying-Ying; Yang, Jun-Bo; Yang, Zhi-Yun; Hu, Yi; Ma, Hong; Soltis, Pamela S.; Soltis, Douglas E.; Li, De-Zhu; Smith, Stephen A.; Yi, Ting-Shuang; et al. (2021). "Gene duplications and phylogenomic conflict underlie major pulses of phenotypic evolution in gymnosperms". Nature Plants. 7 (8): 1015–1025. Bibcode:2021NatPl...7.1015S. bioRxiv 10.1101/2021.03.13.435279. doi:10.1038/s41477-021-00964-4. PMID 34282286. S2CID 232282918.
- ^ Stull, Gregory W.; et al. (2021). "main.dated.supermatrix.tree.T9.tre". Figshare. doi:10.6084/m9.figshare.14547354.v1.