| Camellia sinensis | |
|---|---|
| Camellia sinensis foliage | |
| Scientific classification | |
| Kingdom: | Plantae |
| Clade: | Tracheophytes |
| Clade: | Angiosperms |
| Clade: | Eudicots |
| Clade: | Asterids |
| Order: | Ericales |
| Family: | Theaceae |
| Genus: | Camellia |
| Species: | C. sinensis |
| Binomial name | |
| Camellia sinensis | |
| Synonyms | |
| |
Camellia sinensis, commonly known as tea plant, tea shrub, and tea tree, is a species of evergreen shrub in the flowering plant family Theaceae. The leaves harvested from C. sinesis are brewed into tea.
Originally native to the highlands of the Hengduan–Purvanchal region between southwestern China, northern Myanmar and northeastern India, the leaves, buds and stems of C. sinensis are harvested by humans to produce tea, leading to its artificial introduction and cultivation as valuable cash crops in many other parts of the world, with China, India and Kenya being the three largest tea-producing countries.
Tea leaves used to make white tea, yellow tea, green tea, oolong, dark tea (which includes pu'er tea) and black tea (aka red tea) are all made from two of the five varieties of C. sinensis that form the bulk of the tea crops now grown, C. sinensis var. sinensis and C. sinensis var. assamica, but are processed differently to attain varying levels of oxidation, with black tea being the most oxidized and white being the least. Kukicha (twig tea) is also made from C. sinensis, but uses only twigs and stems rather than leaves and buds.
The name sinensis is a compound meaning "from China" in Botanical Latin. The two parts are sin from Latin meaning China and -ensis the suffix meaning place of origin.
The generic name Camellia is taken from the Latinized name of Rev. Georg Kamel, SJ (1661–1706), a Moravian-born Jesuit lay brother, pharmacist, and missionary to the Philippines.
Camellia sinensis is widely known by the common name tea tree, a name in use since 1760. However, it is also used to refer to shrubs or trees of the myrtle family from Australia and New Zealand, most frequently species in Leptospermum or Melaleuca the first usage dating to 1790. Tea trees are also variously called tea-bushes, tea-shrubs, and tea-plants.
Camellia sinensis is a woody shrub or tree that is typically 1 to 5 m (3.3 to 16.4 ft) tall, but can be as tall as 20 m (66 ft). It is usually trimmed to a height of about 1 m (3.3 ft) with a flat top when in commercial tea plantations. The bark on trunks is smooth and gray with a yellow or brown tone. Young branches are yellow with a gray cast to them while new twigs are red-purple with white hairs. In older trees the trunk reaches as much as 40 cm in diameter.
In seedlings the taproot is dominant, but in mature plants the distribution of roots depends upon individual plant characteristics and growing conditions. In areas with shallow soils or high water tables tea bushes will have a shallow, fibrous root system while in areas with deep soils root have been found at depths of 5.5 m. Tea bushes reach peak productivity at ages of 30 to 50 years, but can remain productive for over a century.

The leaves are an attractive green and tend to be smaller on cultivated plants than wild ones, ranging in size from 4 to 22 cm (1.5 to 8.5 in) and a width of 2 to 7.7 cm (0.8 to 3.0 in). Their shape is elliptic, oblong-elliptic, or oblong, and they have a leathery texture. The upper surface is shining dark green and hairless while the underside is pale green and can be hairless or pubescent, covered in plant hairs. The center vein is raised above the surface of the leaf on both sides as are the smaller seven to nine veins to each side. The netlike veins between are also visible. The leaf tip has a wide angle and the edges are serrate to serrulate, having asymmetrical teeth that point forwards to very fine serrations.


The flowers are white, 2.5 to 3.5 cm (1 to 1.5 in) across with six to eight petals. They bud in the leaf axils and can be solitary or have up to three in a cluster. On the back of the flower there will be five sepals 3–5 mm long. One to three of the petals will be somewhat sepal-like and hidden behind the five visible at the front of the flower. The center of the flower is filled with numerous hairless stamens 8–13 mm long. They are arranged in as many as five concentric circles called whorls.

The fruit is a capsule with globe shape, usually flattened at the ends and measuring 1–1.5 cm top to bottom and 1.5-3.5 cm in diameter. Each fruit will have one to three round chambers with one or two seeds in each. The seeds are brown to almost black in color and are round, half-spheres, or have mulpile flat faces. They measure 1 to 2 cm and are hairless.
Linnaeus did not consider this plant a Camellia but placed it in a separate genus Thea. Then in 1818, Robert Sweet merged the two genera, selecting Camellia for the merged genus, and shifted all the former Thea species to that genus.
Five varieties of Camellia sinensis are accepted:
Camellia sinensis has 82 synonyms of the species or of four of its five varieties. This includes 45 species names.
| Name | Year | Rank | Synonym of: | Notes |
|---|---|---|---|---|
| Camellia angustifolia Hung T.Chang | 1981 | species | var. pubilimba | = het. |
| Camellia arborescens Hung T.Chang, F.L.Yu & P.S.Wang | 1983 | species | var. sinensis | = het. |
| Camellia assamica (Royle ex Hook.) C.D.Darl & Jan.Ammal | 1945 | species | var. assamica | ≡ hom. |
| Camellia assamica var. kucha Hung T.Chang, H.S.Wang & B.H.Chen | 1983 | variety | var. assamica | = het. |
| Camellia assamica subsp. lasiocalyx (G.Watt) W.Wight | 1962 | subspecies | var. assamica | = het. |
| Camellia assamica var. polyneura (Hung T.Chang, Y.J.Tan & P.S.Wang) Hung T.Chang | 1998 | variety | var. assamica | = het. |
| Camellia bohea (L.) Sweet | 1818 | species | var. viridis | = het. |
| Camellia dehungensis Hung T.Chang, H.S.Wang & B.H.Chen | 1983 | species | var. dehungensis | ≡ hom. |
| Camellia dehungensis Hung T.Chang & B.H.Chen | 1984 | species | var. dehungensis | = het., nom. illeg. |
| Camellia dishiensis F.C.Zhang, X.Y.Chen & G.B.Chen | 1990 | species | var. pubilimba | = het. |
| Camellia formosensis (Masam. & S.Suzuki) M.H.Su, C.F.Hsieh & C.H.Tsou | 2009 | species | var. viridis | = het. |
| Camellia kucha (Hung T.Chang, H.S.Wang & B.H.Chen) Hung T.Chang | 2008 | species | var. assamica | = het. |
| Camellia longlingensis F.C.Zhang, G.B.Chen & M.D.Tang | 1990 | species | var. viridis | = het. |
| Camellia manglaensis Hung T.Chang, Y.J.Tan & P.S.Wang | 1983 | species | var. dehungensis | = het. |
| Camellia multisepala Hung T.Chang, Y.J.Tan & P.S.Wang | 1983 | species | var. assamica | = het. |
| Camellia oleosa (Lour.) Rehder | 1937 | species | var. virescens | ≡ hom. |
| Camellia parvisepala Hung T.Chang | 1981 | species | var. pubilimba | = het. |
| Camellia parvisepaloides Hung T.Chang, H.S.Wang & B.H.Chen | 1983 | species | var. dehungensis | = het. |
| Camellia polyneura Hung T.Chang, Y.J.Tan & P.S.Wang | 1983 | species | var. assamica | = het. |
| Camellia scottiana Choisy | 1855 | species | var. assamica | = het., not validly publ. |
| Camellia sinensis var. dulcamara Q.U.Le & D.L.Nguyen | 2020 | variety | var. assamica | = het. |
| Camellia sinensis f. formosensis (Masam. & S.Suzuki) Kitam. | 1950 | form | var. virescens | ≡ hom. |
| Camellia sinensis var. kucha Hung T.Chang & S.S.Wang | 1984 | variety | var. assamica | = het. |
| Camellia sinensis var. lasiocalyx (G.Watt) A.P.Das & C.Ghosh | 2016 | variety | var. assamica | = het. |
| Camellia sinensis f. macrophylla (C.Morren) Kitam. | 1950 | form | var. virescens | = het. |
| Camellia sinensis f. parvifolia (Miq.) Sealy | 1958 | form | D. viridis | ≡ hom. |
| Camellia sinensis f. rosea (Makino) Kitam. | 1950 | form | D. viridis | ≡ hom. |
| Camellia sinensis f. ticinensis (Pollacci & Gallotti) Ardenghi | 2020 | form | var. virescens | = het., cited basionym not validly publ. |
| Camellia sinensis var. waldenae (S.Y.Hu) Hung T.Chang | 1981 | variety | var. virescens | ≡ hom. |
| Camellia tenuistipa Orel, Curry & Luu | 2015 | species | var. assamica | = het. |
| Camellia thea Link | 1822 | species | C. sinensis | ≡ hom., nom. superfl. |
| Camellia thea var. assamica (Royle ex Hook.) Boerl. | 1901 | variety | var. assamica | ≡ hom. |
| Camellia thea var. bohea (L.) G.Watt | 1907 | variety | D. viridis | ≡ hom. |
| Camellia thea var. lasiocalyx G.Watt | 1907 | variety | var. assamica | = het. |
| Camellia thea var. stricta (Hayne) G.Watt | 1907 | variety | var. virescens | = het. |
| Camellia thea f. ticinensis Pollacci & Gallotti | 1940 | form | var. virescens | = het., nom. nud. |
| Camellia thea var. viridis (L.) G.Watt | 1907 | variety | var. virescens | = het. |
| Camellia theifera Griff. | 1854 | species | var. assamica | = het. |
| Camellia theifera var. assamica (Royle ex Hook.) Greshoff | 1893 | variety | var. assamica | ≡ hom. |
| Camellia theifera var. macrophylla (C.Morren) Matsum. | 1883 | variety | var. viridis | = het. |
| Camellia viridis Sweet | 1818 | species | D. viridis | ≡ hom. |
| Camellia waldenae S.Y.Hu | 1977 | species | var. viridis | = het. |
| Thea assamica Royle ex Hook. | 1847 | species | var. assamica | ≡ hom. |
| Thea bohea L. | 1762 | species | var. virescens | = het. |
| Thea bohea var. laxa Aiton | 1789 | variety | var. virescens | = het. |
| Thea bohea var. stricta Aiton | 1789 | variety | var. virescens | = het. |
| Thea cantoniensis Lour. | 1790 | species | var. viridis | = het. |
| Thea chinensis Sims | 1807 | species | var. virescens | ≡ hom., orth. var. |
| Thea cochinchinensis Lour. | 1790 | species | var. assamica | = het. |
| Thea formosensis Masam. & S.Suzuki | 1937 | species | var. virescens | = het. |
| Thea grandifolia Salisb. | 1796 | species | var. viridis | = het. |
| Thea latifolia Lodd. ex Sweet | 1839 | species | var. virescens | ≡ hom. |
| Thea laxa Staunton | 1798 | species | D. viridis | ≡ hom. |
| Thea longifolia Nois. ex Steud. | 1821 | species | var. viridis | = het., not validly publ. |
| Thea macrophylla (C.Morren) Makino | 1918 | species | var. viridis | = het. |
| Thea olearia Lour. ex Gomes Mach. | 1868 | species | var. viridis | = het. |
| Thea oleosa Lour. | 1790 | species | var. viridis | = het. |
| Thea parvifolia Salisb. | 1796 | species | var. virescens | = het. |
| Thea sasanqua var. oleosa (Lour.) Pierre | 1887 | variety | var. viridis | = het. |
| Thea sinensis L. | 1753 | species | C. sinensis | ≡ hom. |
| Thea sinensis var. assamica (Royle ex Hook.) Pierre | 1887 | variety | var. assamica | ≡ hom., nom. illeg. |
| Thea sinensis var. assamica Guilf. | 1883 | variety | var. assamica | = het. |
| Thea sinensis var. bohea (L.) K.Koch | 1853 | variety | var. viridis | = het. |
| Thea sinensis var. cantoniensis (Lour.) Pierre | 1887 | variety | var. virescens | ≡ hom. |
| Thea sinensis var. diffusa C.Morren | 1835 | variety | D. viridis | ≡ hom. |
| Thea sinensis var. macrophylla C.Morren | 1835 | variety | var. virescens | = het. |
| Thea sinensis var. parvifolia Miq. | 1867 | variety | var. viridis | = het. |
| Thea sinensis var. pubescens Pierre | 1887 | variety | var. virescens | = het. |
| Thea sinensis var. rosea Makino | 1905 | variety | var. viridis | = het. |
| Thea sinensis var. rugosa C.Morren | 1835 | variety | var. viridis | = het. |
| Thea sinensis var. stricta C.Morren | 1835 | variety | D. viridis | ≡ hom. |
| Thea sinensis var. viridis Pierre | 1887 | variety | var. virescens | = het. |
| Thea stricta Hayne | 1821 | species | var. viridis | = het. |
| Thea viridis L. | 1762 | species | var. viridis | = het. |
| Thea viridis var. assamica (Royle ex Hook.) Choisy | 1855 | variety | var. assamica | ≡ hom. |
| Thea viridis var. bohea (L.) Vent. | 1799 | variety | var. virescens | = het. |
| Thea viridis variegata J.Dix | 1861 | var. viridis | = het. | |
| Thea yersinii A.Chev. ex Gagnep. | 1943 | species | var. assamica | = het., without a Latin descr. |
| Theaphylla anamensis Raf. | 1838 | species | var. viridis | = het. |
| Theaphylla cantoniensis (Lour.) Raf. | 1838 | species | var. viridis | = het. |
| Theaphylla laxa (Aiton) Raf. | 1838 | species | var. viridis | = het. |
| Theaphylla viridis (Sweet) Raf. | 1838 | species | var. virescens | ≡ hom. |
| Notes: ≡ homotypic synonym; = heterotypic synonym | ||||
In 2017, Chinese scientists sequenced the genome of C. s. var. assamica. It contains about three billion base pairs, which is larger than most plants previously sequenced.
The Cambodia type tea ("C. assamica subsp. lasiocalyx") was originally considered a type of Assam tea. However, later genetic work showed that it is a hybrid between Chinese small leaf tea and Assam tea.

Chinese (small leaf) tea may have originated in southern China possibly with hybridization of unknown wild tea relatives. However, since no wild populations of this tea are known, the precise location of its origin is speculative.
Given their genetic differences forming distinct clades, Chinese Assam type tea (C. s. var. assamica) may have two different parentages – one being found in southern Yunnan (Xishuangbanna, Pu'er City) and the other in western Yunnan (Lincang, Baoshan). Many types of Southern Yunnan Assam tea have been hybridized with the closely related species Camellia taliensis. Unlike Southern Yunnan Assam tea, Western Yunnan Assam tea shares many genetic similarities with Indian Assam type tea (also C. s. var. assamica). Thus, Western Yunnan Assam tea and Indian Assam tea both may have originated from the same parent plant in the area where southwestern China, Indo-Burma, and Tibet meet. However, as the Indian Assam tea shares no haplotypes with Western Yunnan Assam tea, Indian Assam tea is likely to have originated from an independent domestication. Some Indian Assam tea appears to have hybridized with the species Camellia pubicosta.
Assuming a generation of 12 years, Chinese small leaf tea is estimated to have diverged from Assam tea around 22,000 years ago; this divergence would correspond to the last glacial maximum, while Chinese Assam tea and Indian Assam tea diverged 2,800 years ago.
Chinese small leaf type tea was introduced into India in 1836 by the British and some Indian Assam type tea (e.g. Darjeeling tea) appear to be genetic hybrids of Chinese small leaf type tea, native Indian Assam, and possibly also closely related wild tea species.

The origins of tea plants are obscured by their long history of cultivation. The natural range is unknown, though it is reasonably certain that the species comes from East Asia with the exact location being debated by experts.
The borderlands theory suggests the species originated in the borderlands of far eastern India, north Myanmar, and southwestern China. Alternatively, other experts point to an origin to the northeast in Yunnan province within China.
In the Plants of the World Online database many more places are listed as part of the native range including not only southcentral and southwest China, Assam and the eastern Himalayas in India, and Myanmar, but also Laos, Thailand, and Vietnam.
Camellia sinensis is mainly cultivated in tropical and subtropical climates, in areas with at least 127 cm (50 in) of rainfall a year. Tea plants prefer a rich and moist growing location in full to part sun, and can be grown in hardiness zones 7–9. However, the species is commercially cultivated from the equator to as far north as Scotland, with the northernmost tea plantation at 59°N latitude on Shapinsay in the Orkney Islands. Many high quality teas are grown at high elevations, up to 2,200 m (7,200 ft), as the plants grow more slowly and acquire more flavour.
Tea plants will grow into a tree if left undisturbed, but cultivated plants are pruned to waist height for ease of plucking. Two principal varieties are used, the small-leaved Chinese variety plant (C. s. var. sinensis) and the large-leaved Assamese plant (C. s. var. assamica), used mainly for black tea. Tea trees can remain productive for many years.
The Chinese plant is a small-leafed bush with multiple stems that reaches a height of some 3 m (9.8 ft). It is native to southeast China. The first tea plant variety to be discovered, recorded, and used to produce tea dates back 3,000 years ago; it yields some of the most popular teas.
C. s. var. waldenae was considered a different species, C. waldenae by SY Hu, but it was later identified as a variety of C. sinensis. This variety is commonly called Waldenae Camellia; it is grown on Sunset Peak and Tai Mo Shan in Hong Kong, and also occurs in Guangxi province.
Three main kinds of tea are produced in India:
Tea culture in Japan from as far back as the 9th century has resulted in various types. Japanese cultivars include:

The seeds of the tea bush (Camellia sinensis) and oil-seed camellia (Camellia oleifera) can be pressed to yield tea oil, a sweetish seasoning and cooking oil.
Tea oil should not be confused with tea tree oil, an essential oil from an unrelated species also called the tea tree (Melaleuca alternifolia). Tea tree oil is used for cosmetics and as alternative medicine, and is not fit for consumption. Tea tree oil is highly toxic when ingested, giving serious side effects that may require medical intervention, especially in children.
Tea leaves are eaten by some herbivores, such as the caterpillars of the willow beauty (Peribatodes rhomboidaria), a geometer moth.
There is no high-quality clinical evidence to indicate that drinking tea has any effect on human health. The United States Food and Drug Administration has approved a specific green tea extract ointment for treating genital warts.
Due to the presence of caffeine in tea leaves, anyone who has a sensitivity to caffeine, has been advised to avoid caffeine, or wishes to avoid the effects of caffeine should reconsider before drinking tea.
Fresh leaves contain about 4% caffeine, as well as related compounds including theobromine. Caffeine functions as a secondary metabolite and acts as a natural pesticide: it can paralyze and kill herbivorous insects feeding on the plant. Caffeine is a purine alkaloid and its biosynthesis occurs in young tea leaves and is regulated by several enzymes. The biosynthetic pathway in C. sinensis is similar to other caffeine-producing plants such as coffee or guayusa. Analysis of the pathway was carried out by harvesting young leaves and using reverse transcription PCR to analyze the genes encoding the major enzymes involved in synthesizing caffeine. The gene TCS1 encodes caffeine synthase. Younger leaves feature high concentrations of TCS1 transcripts, allowing more caffeine to be synthesized during this time. Dephosphorylation of xanthosine-5'-monophosphate into xanthosine is the committed step for the xanthosines entering the beginning of the most common pathway. A sequence of reactions turns xanthosine (9β-D-ribofuranosylxanthine) into 7-methylxanthosine, then 7-methylxanthine, then theobromine (3,7-dimethylxanthine), and finally into caffeine (1,3,7-trimethylxanthine).

This section may contain material unrelated to the topic of the article. (June 2026) |
The first edition of Linnaeus's Species Plantarum published in 1753 suggested calling the tea plant Thea sinensis...
The generic names Thea L. (Sp. Pl.: 515. 24 Mai 1753), and Camellia L. (Sp. Pl.: 698. 16 August 1753; Gen. Pl., ed. 5: 311. 1754), are treated as having been published simultaneously on 1 May 1753. … the combined genus bears the name Camellia, since Sweet (Hort. Suburb. Lond.: 157. 1818), who was the first to unite the two genera, chose that name, and cited Thea as a synonym.
{{cite web}}: CS1 maint: periodical has ISBN (link)