免费文献传递   相关文献

Three new species of Piperaceae from Thailand



全 文 :植 物 分 类 学 报 44 (4): 447–453(2006) doi:10.1360/aps040163
Acta Phytotaxonomica Sinica http://www.plantsystematics.com
———————————
Received: 19 April 2005 Accepted: 14 August 2005
* Author for correspondence. E-mail: raccha@kku.ac.th; Tel.: +66-4334-2908 ext. 209; Fax: +66-4336-4169.
Three new species of Piperaceae from Thailand
1CHAVEERACH Arunrat* 2SUDMOON Runglawan 2TANEE Tawatchai 1MOKKAMUL Piya
1(Department of Biology, Faculty of Science, Khon Kaen University, Khon Kaen 40002, Thailand)
2(Department of Biochemistry, Faculty of Science, Khon Kaen University, Khon Kaen 40002, Thailand)
Abstract Three new species of Piperaceae, Piper dominantinervium A. Chaveerach & P.
Mokkamul, P. pilobracteatum A. Chaveerach & R. Sudmoon from southern Thailand, and P.
phuwuaense A. Chaveerach & T. Tanee from northeastern Thailand, are described and
illustrated. P. phuwuaense is considered rare and endemic to Phu Wua Wildlife Sanctuary.
Morphological differences between the new species and related taxa are discussed.
Key words Piper, Piper dominantinervium A. Chaveerach & P. Mokkamul, Piper
phuwuaense A. Chaveerach & T. Tanee, Piper pilobracteatum A. Chaveerach & R. Sudmoon,
Piperaceae, new species, Thailand.
The genus Piper L. is estimated to contain over 1000 species which are distributed
mainly in tropical regions of the world. Several species have great economic and cultural
importance and are used as foods, medicines, stimulants, antiseptics and antioxidants.
Moreover, their essential oil and leaf extracts possess activities against several bacterium
strains and fungi. Leaves of P. hispidinervum C. DC. contain a high level of safrole
(83%–93%) which is an important raw material for chemical industries. Two derivatives of
safrole are heliotropin, which is widely used as a fragrance and flavoring agent, and piperonyl
butoxide, which is a vital ingredient of pyretroid insecticides. There are other Piper species
with possibilities for extracting safrole and can be cultivated in the local communities.
Because of the usefulness of many known Piper species, this diverse plant group should be
studied in more depth to determine more economic and medicinal uses of other species.
We have been concentrating our work on species diversity of this genus in Thailand.
Many species have been reported recently (Chaveerach & Picheansoonthon, 2004) and some
of these species descriptions are in the process of publication. It is evident that the plant
diversity and taxonomy in Thailand have not been completed.
Taxonomic identifications of the three new species described in this paper were
investigated based on references available from Baker and Van Den Bakhuizen (1963),
Chaveerach et al. (2002), Chaveerach (2003), Chaveerach and Picheansoonthon (2004),
Cheng et al. (1999), Chew (1972), Gardner (2003), Hayata (1911), Henderson (1959), Heyne
(1987), Ho (1960, 1991), Hooker (1885), Huber (1988), Keng (1990), Lin and Lu (1996),
Long (1984), Merrill (1912), Ridley (1967), Royen (1982), and Yuncker (1972). Type
specimens were checked from many herbaria. Botanical illustrations of these studied
specimens are shown.
1. Piper dominantinervium A. Chaveerach & P. Mokkamul, sp. nov. Fig. 1
Haec species similis P. diospyrifolio Kunth, sed a quo differt foliorum laminis oblongis,
basi aequalibus vel inaequalibus, apice acuminatis, venis utrinque pilosis, spica mascula
conspicue breviore, staminibus 4, bracteis glabris.
Southern Thailand. Phang Nga: Sriphang Nga National Park, alt. 100 m, evergreen
Acta Phytotaxonomica Sinica Vol. 44 448

Fig. 1. Piper dominantinervium A. Chaveerach & P. Mokkamul. A, leaves toward base of stem; B, leaves toward apex
of stem with male spike; C, male spike; D, anthers. Drawn by P. Mokkamul from the type gathering, A. Chaveerach 63498
(epiphytic branch) and A. Chaveerach 63499 (flowering branch).
No. 4 CHAVEERACH Arunrat et al.: Three new species of Piperaceae from Thailand 449
forest, 2000-10-19, A. Chaveerach 63498-500 (holotype, BK; isotype, Department of
Biology, Faculty of Science, Khon Kaen University, Thailand). Ranong: Ngao Waterfall
National Park, alt. 100 m, 2000-10-18, A. Chaveerach 492 (BK); ibid., Poonyaban waterfall,
alt. 200 m, 2000-10-18, A. Chaveerach 493 (BK).
Climber on trees, nodes distinctly jointed, swollen, brownish-blackish when dry. Stem
stout, furrowed when dry. Leaves toward base of stem coriaceous, oblong to narrowly elliptic,
7.5–9 cm long, 1.5–3.5 cm broad, apex acute, base subcuneate-cuneate or subrounded; petiole
1–1.2 cm long. Leaves toward apex of stem coriaceous, ovate or narrowly elliptic to elliptic,
12–19 cm long, 2.5–9 cm broad, apex cuspidate, base oblique and unequally sided, auriculate,
dark green, densely yellowish, brownish or reddish-glandular; petiole 0.1–0.2 cm long. Veins
different from most Piper species, many, all from midrib at regular intervals of base to apex
reaching near margin joining with each other. Male spikes pendulous, 5–13 cm long, ca. 0.3
cm in diameter. Peduncle 0.7–1.5 cm long. Bracts elliptic, sessile, margin ciliate. Stamens 2.
Female spikes not seen. Fl. Sept.–Nov.
Piper dominantinervium is similar to P. diospyrifolium Kunth in having veins of leaf
blade dominant and joining, leaf blade on both upper and lower surfaces glandular, but differs
by having leaf blade ovate or narrowly elliptic to elliptic, base oblique and unequally sided,
auriculate, apex cuspidate, male spikes 5–13 cm long, stamens 2, bracts margin ciliate.
Notes: The name of this species refers to one of its most dominant morphological
characteristics: Its veins are different from most Piper species in Thailand, which have basal
veins leaving the base and apical veins leaving the midrib. This species has many veins
branching from the midrib at regular intervals and the apices of the veins extend near the leaf
margin to adjoin with the adjacent veins.
2. Piper phuwuaense A. Chaveerach & T. Tanee, sp. nov. Fig. 2
Haec species insignis foliis basi irregulariter auriculatis, lobo brevi imbricato cum eo
longo, bracteis exstipitatis, basi imbricatis, margine ciliatis.
Northeastern Thailand. Nongkhai: rare and endemic to Phu Wua Wildlife Sanctuary,
alt. 300–400 m, dry evergreen forest, near the border of Thailand and Laos, 2000-11-06, A.
Chaveerach 63501-3 (holotype, BK; isotype, Department of Biology, Faculty of Science,
Khon Kaen University, Thailand).
Climbers on tree and rocks, glabrous, light green. Stem black, furrowed when dry.
Leaves toward base of stem oblong, 7.5–8 cm long, 2.7–3.2 cm broad, apex acuminate, base
cordate with equal basal lobes; petiole 0.5–2 cm long. Veins 4 basal and the one prominent
pair reaching apex, the other transverse veins from midrib joining the prominent pair. Leaves
toward apex of stem obovate, elliptic-oblong, 16–20 cm long, 7.5 cm broad, apex acuminate,
cuspidate, base irregularly auriculate, the short one lobe overlapping the other long lobe.
Veins 7–8, distinctive, adaxially and abaxially prominent, apical pair rising 1.5–3 cm above
base reaching apex, 6–7 basal, other transverse veins near apex from midrib joining the apical
pair before leaf margin. Male spikes pendulous, 2–3 cm long, ca. 0.15 cm in diameter.
Peduncle 1 cm long. Bracts elliptic, rounded, not stalked, base overlapping, margin ciliate.
Stamens 3. Female spikes not seen. Fl. Oct.–Nov.
Piper phuwuaense has very distinctive characters including leaf base irregularly
auriculate, the short one lobe overlapping the long one lobe, bracts not stalked, base
overlapping, margin ciliate, and hence is not similar to any Piper species.
Notes: This species is known only from its type locality, the Phu Wua Wildlife Sanctuary
area, growing in the limestone areas of dry evergreen forest. It is a rare and endemic species.
The specific epithet refers to the type locality of the species, Phu Wua in northeastern Thailand.
3. Piper pilobracteatum A. Chaveerach & R. Sudmoon, sp. nov. Fig. 3
Haec species similis P. kawakamii Hayata, sed a quo differt petiolis glabris, foliorum
Acta Phytotaxonomica Sinica Vol. 44 450

Fig. 2. Piper phuwuaense A. Chaveerach & T. Tanee. A, leaves toward base of stem; B, leaves toward apex of stem
with male spike; C, male spike. Drawn by P. Mokkamul from the type gathering, A. Chaveerach 63501 (epiphytic branch)
and A. Chaveerach 63502 (flowering branch).
No. 4 CHAVEERACH Arunrat et al.: Three new species of Piperaceae from Thailand 451

Fig. 3. Piper pilobracteatum A. Chaveerach & R. Sudmoon. A, leaves toward base of stem; B, leaves toward apex of
stem with fruiting and flowering spikes; C, female spike; D, female flower; E, F, fruiting spikes. Drawn by P. Mokkamul
from the type gathering, A. Chaveerach 320 (epiphytic branch) and A. Chaveerach 63495 (flowering and fruiting branch).
Acta Phytotaxonomica Sinica Vol. 44 452
laminis tenuiter chartaceis, haud undulatis, subtus dense glandulosis, basi rotundatis vel
vadose cordatis, venis alternis et attingentibus marginem, 2 apicalibus orientibus a basi 1–2
cm, stigmatis 4 glabris.
Southern Thailand. Phang Nga: Sri Phang Nga National Park, alt. 100 m, evergreen
forest, 2000-10-19, A. Chaveerach 63495 (holotype, BK; isotype, Department of Biology,
Faculty of Science, Khon Kaen University, Thailand). Nakhon Sri Thammarat: Khao Luang
National Park, alt. 100 m, 2000-08-18, A. Chaveerach 320-321 (BK).
Slender climber, glabrous; stem node dilate, yellow when dry, 2–4 cm in diameter.
Leaves in sunlight thick papery and undulate, in sunshade thinner, ovate, 8.5–13 cm long,
4–6.5 cm broad, apex acuminate, base rounded or subcuneate, yellowish-green to green,
yellowish to light brown when dry, base of blade sparsely hairy, yellowish or brownish
glandular; veins 7, all basal or apical pair arising 0.5 cm above base reaching leaf apex,
prominent adaxially, reticulate veins transverse. Petiole 1–1.2 cm long, base sparsely hairy
and persistent. Male plants not seen. Female spikes cylindrical, straight up, many blooming in
sunlight, 1.5–1.9 cm long, ca. 0.3 cm in diameter. Peduncle 0.8–1 cm long. Bracts circular,
peltate, base of stalk hairy, upper surface hairy, central densely so, margin ciliate, rachis
densely hairy. Stigmas 4 often 5 on a spike. Fruits rounded in sunlight or with a conical point
in sunshade, ca. 0.5 cm in diameter, green, returning to greenish-brown and red when ripe,
fruits distant on a spike. Pedicel ca. 0.2 cm long. Fl. and fr. Sept.–Nov.
Piper pilobracteatum is similar to P. kawakamii Hayata in leaf blade ovate, papery, leaf
base rounded, veins 7, female spike erect, stigmas 4, but differs by having petioles glabrous, leaf
blades thinner papery and not undulate, abaxially densely glandular, base rounded or shallowly
cordate, veins alternate and reaching leaf margin, apical pair of veins arising 1–2 cm above
base, stigmas 4 glabrous.
Notes: The specific epithet refers to the hairy upper surface of bracts.
Acknowledgements We would like to thank Vicente F. Garcia, Ph.D. candidate of Botany,
Integrative Biology, University of California, for checking some type specimens and
reviewing the manuscript of the paper.
References
Baker C A, Bakhuizen Van Den Brink R C. 1963. Flora of Java (Spermatophytes only) Vol. I Gymnospermae,
Families 1–7; Angiospermae, Families 8–110. N.V.P. Noordhoff-Groningen: the Netherlands.
Chaveerach A. 2003. Application of Molecular Techniques in Systematic Study of the Genus Piper in the
Northeast of Thailand. Ph.D. Dissertation. Khon Kaen, Thailand: Khon Kaen University.
Chaveerach A (R), Kunitake H, Nuchadomrong S, Sattayasai N, Komatsu H. 2002. RAPD patterns as a useful
tool to differentiate Thai Piper from morphologically alike Japanese Piper. Science Asia 28: 221–226.
Chaveerach A, Picheansoonthon C. 2004. Preliminary study on the species diversity of the genus Piper in
Thailand. International conference on herbal and traditional eastern medicine: an alternative and
integrative medicine. March 30–31. Macao: University of Macao.
Cheng Y, Xia N, Gilbert M G. 1999. Piperaceae. In: Wu Z-Y, Raven P H eds. Flora of China. Beijing: Science
Press; St. Louis: Missouri Botanical Garden Press. 110–129.
Chew W-L. 1972. The genus Piper (Piperaceae) in New Guinea, Solomon Islands, and Australia. Journal of
the Arnold Arboretum 53: 1–25.
Gardner R O. 2003. Piper (Piperaceae) in New Guinea: the non-climbing species. Blumea 48: 47–68.
Hayata. 1911. Piper kawakamii Hayata. Journal of College Science, Imperial University, Tokyo 30: 234.
Henderson M R. 1959. Pepper Family (Piperaceae). Malayan Wild Flowers Dicotyledons. Kuala Lumpur:
Caxton Press, Ltd.
Heyne K. 1987. Tumbuhan Berguna Indonesia. Jakarta: Jalan Gatot Subroto.
Ho P H. 1960. The Flora of Vietnam. Saigon: Department of National Education.
Ho P H. 1991. An Illustrated Flora of Vietnam. Saigon: Nha Xuat Ban Tre. 288–301.
Hooker J D. 1885. Piperaceae: the Flora of British India. Vol. V. Ashford: L. Reeve & Co., Ltd.
No. 4 CHAVEERACH Arunrat et al.: Three new species of Piperaceae from Thailand 453
Huber H. 1988. Piperaceae. In: Dassanayake M D ed. A Revised Handbook to the Flora of Ceylon. Vol. VI.
Rotterdam: A. A. Balkema.
Keng H. 1990. The Concise Flora of Singapore. Gymnosperms and Dicotyledons. Singapore: Singapore
University Press.
Lin T-T, Lu S-U. 1996. Angiospermae. In: Editorial Committee of the Flora of Taiwan. Flora of Taiwan. 2nd
ed. Taipei: ROC.
Long D G. 1984. Bhutan: Including a record of Plants from Sikkim. Vol. I. Part 2. Edinburgh: Royal Botanic
Garden.
Merrill E D. 1912. A Flora of Manila. Manila: Bureau of Printing.
Ridley H N. 1967. Piperaceae: the Flora of the Malaysia Peninsula. Vol. III: Apetalae. Ashford: L. Reeve &
Co., Ltd.
Royen P V. 1982. The Alpine Flora of New Guinea. Vol. 3. Taxonomic part. Winteraceae to Polygonaceae.
Vaduz: A. R. Gantner.
Yuncker T G. 1972. The Piperaceae of Brazil. Hoehnea 2: 19–366.