Piper betle
publication ID |
https://doi.org/10.3767/000651913X665053 |
persistent identifier |
https://treatment.plazi.org/id/03AF8788-F726-FFA9-930A-BFBA97A77225 |
treatment provided by |
Felipe |
scientific name |
Piper betle |
status |
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3. Piper betle View in CoL L. — Fig. 1d View Fig
Piper betle L. (1753) 28; Quisumb. (1930) 85; R.O. Gardner (2006) 579; (2010) 8. — Type: Herb. Hermann 3: 32, 4: 9 ( BM n.v.) .
Distribution — Widely cultivated in Asia, Malesia, Micronesia, and in Melanesia east to Fiji.
Habitat & Ecology — In gardens and persisting after cultivation, also naturalized; to c. 750 m altitude.
Notes — If the distinctive fruits are not present this species might be confused with P. caninum or P. interruptum , but its leaves tend to dry brownish rather than grey- or olive-brown and do not have large silvery glands. It almost always lacks long hairs, but near the base below (sometimes across both surfaces, best seen on new leaves) there is a scattering of minute (0.05 mm long) appressed hairs.
Labels for New Guinea specimens of P. betle are generally unclear as to naturalization status. However, for the Bismarck Archipelago Peekel (1984: 124) says: “Everywhere wild in scrub ... “.
Quisumbing (1930: pl. 42 (8)) described the stamen of P. betle as having a short stout filament c. 0.6–1 mm diam, with the two rather large anther locules colinear at the filament apex. Dehiscence takes place at or just below the bract-heads, and is by a continuous apical slit. As in other regions, female spikes can also bear stamens, e.g. in Darbyshire 1018.
BM |
Bristol Museum |
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