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Malesian Euphorbiaceae Newsletter 1
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Tree Flora of Sabah and Sarawak Project
Example of Flora Malesiana Format
The Flora Malesiana project officially started in 1950, but was already initiated by Prof. Van Steenis in the 40’s. The project’s aim is to describe the flora of the Indonesian Archipelago, a flora estimated to comprise 40,000 species of Angiosperms, Gymnosperms, and ferns. The Angiosperms and Gymnosperms are being published in series 1 of the Florea, and the ferns in series 2. Up to now, including the volumes to be published in 1993, a quarter of the flora has been finished.
The Malesian region comprises the following areas (see map on inside covers):
- Malay Peninsula, from Isthmus of Kra southwards |
- Celebes (or Sulawesi) |
- Sumatra |
- Lesser Sunda Islands |
- Java |
- Moluccas |
- Borneo |
- New Guinea (incl. Bougainville Isl.) |
- Philippines |
The areas contain the following countries:
- Malaysia (States: Malaya on Malay Peninsula, Sabah and Sarawak on Borneo)
- Singapore (southern tip of Malay Peninsula)
- Indonesia (Sumatra, Borneo-Kalimantan, Java, Lesser Sunda Islands, Celebes, Moluccas, New Guinea-Irian Jaya)
- Brunei Darussalam (on Borneo)
- Philippines
- Papua New Guinea
The larger part of the Malesian area consists of the Indonesian islands. Two countries are present on the Malay Peninsula (Malaysia and Singapore), 4 different states/countries on Borneo (Kalimantan, the Indonesian part of Borneo; Sabah and Sarawak, the Malaysian part of Borneo; and Brunei), and 2 countries on New Guinea (Irian Jaya, the Indonesian western half; and Papua New Guinea, the eastern half).
A quarter of the flora has been treated, the remaining threequarters have to be revised in the next 20 years. This means that the project has to accelarate very fast. Several options are available to do so. A computerisation of the project will increase efficiency, for this purpose LBASE is being developed in Leiden. LBASE will include a literature database, specimen data, and distribution data. The project will be tightly managed. The format will be simplified (see below). And, to save most time, the research will switch from semi-monographic to more compilatory.
At the end of last year a start was made with the revision of the Malesian Euphorbiaceae for Flora Malesiana. This project will be a kind of pilot project under the new management. The Euphorbiaceae are very suitable for compilatory work as Airy Shaw has revised almost all of them for the greater part of Malesia with flora treatments being available for the remaining parts. The planning for the treatment of the Euphorbiaceae is 10 years, which means that they should be finished in 2002. As I can never accomplish this by myself many botanists have been invited to collaborate. Many positive reactions were received from about half of the people who responded. We are glad that such a high degree of enthousiam exists.
In order to start and maintain a constant flow of information among all contributors this newsletter was started. The newsletter will be issued twice per year. Those who like to publish information in it are more than welcome.
For the time being I will coordinate the revision of the Malesian Euphorbiaceae. In the future the Royal Botanic Gardens in Kew may take over as they have built an enormous knowledge of Asian and African Euphorbiaceae. Mrs. Dr. S.C. Holmes and Dr. A. Radcliffe-Smith still work on African Euphorbs, while Airy Shaw, the main revisor of Malesian Euphorbs, has worked in Kew. Plans in Kew exist to extent their involvement in the Flora Malesiana project and this may include an extra position for a Euphorbiaceae specialist.
As coordinator I will employ the following activities:
- Motivate specialists to join the project. See list below.
- Provide them with literature and information if necessary.
- Arrange loans of Leiden specimens.
- Create and maintain a literature database per species
- Provide a regular newsletter, probably issued twice per year.
- Keep all contributors to a time schedule (maximum 10 years).
- Coordinate contacts amont the contributors.
- Apply for funds to enable contributors to visit Leiden and Kew. Citizens of an EC-country can apply for EC travel funds as part of the ‘human capital and mobility’ programme. The Dutsch Science Foundation (NWO) also provides funds for visiting scientists, however, these only include wages, no travel expanses.
- Apply for PhD scholarships. Mrs. Anne Schot is the first PhD ‘student’(not a study in Holland, but a regular job), she is revising Aporosa. The next scholarship will be for the revision of Baccaurea.
- Prepare identification keys on male flowers, female flowers, and fruits.
My first task in the next two to three years wil be to gain insight in the family, to prepare the keys which can be used for a preliminary identification, and to revise the monotypic genera as far as no contributors will be found. This will be followed by a revision of large genera like Antidesma, Glochidion, and Mallotus.
The following literature provides the backbone for the compilatory treatment of the Euphorbiaceae:
- Thailand: Airy Shaw, H.K. 1971. The Euphorbiaceae of Siam. Kew Bull. 26: 101—363.
- Malay Peninsula: Whitmore, T.C. 1973. Euphorbiaceae. In: T.C. Whitmore (ed.), Tree flora of Malaya 2: 34—136. Longman, London. N.B. trees only!
- Sumatra: Airy Shaw, H.K. 1981. The Euphorbiaceae of Sumatra. Kew bull. 36: 239—374.
- Java: Backer, C.A. & R.C. Bakhuizen van den Brink jr. 1963. Flora of Java 1: 441—505. Noordhoff, Groningen.
- Borneo: Airy Shaw, H.K. 1975. The Euphorbiaceae of Borneo. Kew Bull. Add. Ser. 4: 1—245.
- Philippines: Airy Shaw, H.K. 1983. An alphabetical enumeration of the Euphorbiaceae of the Philippine Islands: 1—56. Royal Botanic Gardens, Kew. N.B. checklist!
- Celebes, Moluccas, Lesser Sunda Islands: Airy Shaw, H.K. 1982. The Euphorbiaceae of Central Malesia (Celebes, Moluccas, Lesser Sunda Is.). Kew Bull. 37: 1—40. N.B. checklist!
- New Guinea: Airy Shaw, H.K. 1980. The Euphorbiaceae of New Guinea. Kew Bull. Add. Ser. 8: 1—243.
The most important herbaria for Malesian material are (abbreviations as in Index Herbariorum, addresses below):
Inside the Malesian region: BO (Bogor, Indonesia), BRUN (Bandar Seri Begawan, Brunei), KEP (Kepong, Malaysia), LAE (Lae, Papua New Guinea), PNH (Manila, Philippines), SAN (Sandakan, Malaysia), SAR (Sarawak, Malaysia), SING (Singapore).
Outside the Malesian region: A (Harvard, U.S.A.), BM (London, England), BRI (Indooroopilly, Australia), K (Kew, England), L (Leiden, Netherlands), NSW (Sydney, Australia), NY (New York, U.S.A.), P (Paris), US (Washington, U.S.A.).
Type material can be located in many more herbaria. Quite often Beccari specimens are indicated as types, the holotypes are stored in FI (Firenze, Italy), but cannot be obtained on loan. The herbaria, in which type material is stored, can be traced with the Cyclopedia of Collectors, compiled by Mrs. Van Steenis-Kruseman in volumes 1, 5, and 8 of Flora Malesiana series 1 (Van Steenis editor). Per collector a list of the herbariu, in which his/her main collections are stored, is provided. The Cyclopedia is also useful to obtain information about the exact collecting localities as the collecting trips are also described per collector. In Leiden a user-friendly database program, called COOR, has been made in dBase III+, which can be used to extract the coordinates of collecting localities. Teh program and the data can be obtained free-of-charge from me.
An example of the format of a genus revision for Flora Malesiana is added as appendix, together with a prospectus of the Flora Malesiana Foundation.
A genus description contains:
- Block with Accepted genus name, synonym genus names, author names, litereture references and type references; all arranged chronologically per type per name.
- Genus description.
- Block with several headings: Distribution, ecology, and habitat, notes, etc. Vernacular names are prefarably omitted unless the validity has been checked.
- Identification key to the species and infraspecific ranks; a bracketed key, not an indented key anymore.
- Species descriptions containing the same elements as the genus description. Species arranged alphabetically.
The following list shows the Malesian Euphorb genera in alphabetical order, the number of species estimated world-wide, estimated within Malesia, presence world-wide, and the contributor.
Genus |
World |
Malesia |
Presence |
Contributor |
Acalypha |
430 |
25 |
Pantropical |
|
Actephila |
35 |
6 |
Indomalesia to Australia |
|
Aporosa |
75 |
60 |
Indomalesia to Solomons |
|
Agrostistachys |
9 |
5 |
India to W Malesia |
|
Alchornea |
70 |
3 |
Tropical |
|
Aleurites |
6 |
1 |
W Pacific |
|
Alphandia |
3 |
1 |
New Guinea, W Pacific |
|
Annesijoa |
1 |
1 |
New Guina |
|
Antidesma |
160 |
60 |
Old world tropics and warm areas |
|
Ashtonia |
2 |
2 |
Malay Penin., Borneo |
|
Austrobuxus |
17 |
1 |
Malesia to Fiji |
|
Baccaurea |
80 |
50 |
Indomalesia to W Pacific |
|
Baliospermum |
6 |
1 |
India to central Malesia |
|
Bischofia |
1 |
1 |
Indomalesia |
|
Blachia |
12 |
1 |
India to central Malesia |
|
Blumeodendron |
6 |
6 |
Andamans, Malesia |
Kochummen |
Borneodendron |
1 |
1 |
N Borneo |
|
Botryophora |
0 |
1 |
SE Asia, W Malesia |
|
Breynia |
25 |
10 |
China to Australia and New Caledonia |
|
Bridelia |
60 |
15 |
Old world tropics |
|
Cephalomappa |
5 |
5 |
S China, Malesia |
Widuri |
Chaetocarpus |
11 |
1 |
Pantropical |
|
Cheilosa |
2 |
1 |
W Malesia |
|
Chondrostylis |
2 |
1 |
SE Asia, W Malesia |
|
Choriceras |
1 |
1 |
S New Guinea, Australia |
|
Chorisandrachne |
1 |
1 |
Thailand |
|
Chrozophora |
12 |
1 |
Mediterranean, trop. Africa to India |
|
Cladogynos |
1 |
1 |
SE Asia, Malesia |
|
Claoxylon |
80 |
40 |
Old world tropics |
|
Cleidion |
25 |
3 |
Pantropical |
|
Cleistanthus |
130 |
40 |
Old world tropics |
|
Clonostylis |
0 |
1 |
Synonym of Spathiostemon |
|
Cnesmone |
10 |
1 |
Assam to W Malesia |
|
Codiaeum |
6 |
10 |
Malesia to Pacific |
MSc student Bogor |
Croton |
750 |
35 |
Tropical and warm areas |
|
Dalechampia |
110 |
1 |
Warm areas, esp. America |
|
Dicoelia |
3 |
1 |
W Malesia |
|
Dimorphocalyx |
12 |
5 |
Indomalesia to Australia |
|
Doroxylon |
1 |
1 |
Malesia |
|
Drypetes |
200 |
50 |
E Asia, S Africa |
|
Elateriospermum |
1 |
1 |
S Thailand, Malay Pen. |
Kochummen |
Endospermum |
13 |
10 |
SE Asia to Fiji |
Kochummen |
Epiprinus |
6 |
1 |
Assam to W Malesia |
|
Erismanthus |
2 |
2 |
SE Asia to W Malesia |
|
Erythrococca |
30 |
1 |
Trop. & S Africa |
|
Euphorbia |
1600 |
30 |
Cosmopolitan |
|
Excoecaria* |
40 |
5 |
Old world tropics |
|
Fahrenheitia |
4 |
1 |
India to central Malesia |
Kochummen |
Flueggea |
13 |
2 |
Tropical |
|
Fontainea |
2 |
1 |
New Guinea, Australia, New Caledonia |
|
Galearia |
6 |
5 |
SE Asia to Solomons |
Metilistina Sasinggla |
Glochidion |
300 |
150 |
Tropical |
|
Hevea |
9 |
1 |
Amazonia |
|
Homalanthus* |
35 |
15 |
Trop. Asia to Australia |
|
Homonoia |
2 |
1 |
SE Asia, Malesia |
|
Hura |
2 |
1 |
Trop. America |
|
Hymenocardia |
5 |
1 |
Africa, SE Asia to Sumatra |
|
Jatropha |
170 |
5 |
Tropical and warm areas, N America |
|
Kairothamnus |
1 |
1 |
New Guinea |
|
Koilodepas |
10 |
5 |
India to Malesia |
MSc student Bogor |
Lasiococca |
3 |
1 |
E Himalayas to Malay Pen. |
|
Leptopus |
20 |
1 |
W Himalayas to Australia |
|
Macaranga |
240 |
125 |
Old world tropics |
|
Mallotus |
140 |
50 |
Old world tropics |
Mohamad |
Manihot |
98 |
3 |
Tropical and warm America |
|
Margaritaria |
4 |
1 |
Tropical |
|
Megistostigma |
4 |
1 |
SE Asia, W Malesia |
|
Melanolepis |
2 |
1 |
SE Asia to Pacific |
|
Micrococca |
14 |
1 |
Old world tropics |
|
Microdesmis |
10 |
2 |
Trop. Africa, SE Asia, W Malesia |
|
Moultonianthus |
1 |
1 |
Sumatra, Borneo |
|
Neoroeptera |
1 |
1 |
NE Australia |
|
Neoscortechinia |
4 |
5 |
Burma to Solomons |
|
Neotrewia |
1 |
1 |
Malesia |
|
Omphalea |
20 |
3 |
Tropical |
|
Ostodes |
4 |
1 |
E Himalayas to Borneo |
|
Pachystylidium |
1 |
1 |
India to Central Malesia |
|
Pedilanthes |
14 |
1 |
N to tropical America |
|
Petalostigma |
7 |
1 |
New Guinea, Australia |
|
Phyllanthus |
600 |
80 |
Tropical and warm areas |
|
Pimelodendron |
8 |
4 |
Malesia |
Kochummen |
Pterococcus |
1 |
1 |
Indomalesia |
|
Ptychopyxis |
13 |
10 |
Thailand to W Malesia, E New Guinea |
Murdoyuwono |
Reutealis |
1 |
1 |
Philippines |
|
Richeriella |
2 |
1 |
SE China to central Malesia |
|
Ricinus |
1 |
1 |
Europe to Africa and Middle East |
|
Sapium |
100 |
3 |
Tropical and warm areas to Patagonia |
Kochummen |
Sauropus |
40 |
5 |
SE Asia, Indomalesia |
|
Sebastiana* |
100 |
2 |
Tropical and warm areas |
|
Securinega |
20 |
0 |
Tropical and warm areas |
|
Spathiostemon |
3 |
1 |
Thailand, W Malesia, New Guinea |
|
Stillingia* |
30 |
1 |
Tropical and warm areas |
|
Strophioblachia |
2 |
1 |
SE Asia to central Malesia |
|
Sumbaviopsis |
1 |
1 |
Assam to W Malesia |
|
Suregada |
40 |
3 |
Old world tropics |
|
Syndyophyllum |
1 |
1 |
Sumatra, Borneo, New Guinea |
|
Tapoides |
1 |
1 |
Borneo |
|
Trewia |
2 |
1 |
Himalayas to Hainan |
|
Trigonopleura |
1 |
1 |
W Malesia |
|
Trigonostemon |
45 |
15 |
Indomalesia |
|
Wetria |
1 |
1 |
SE Asia to W Malesia, New Guinea |
|
* Mr. H.-J. Esser indicates that the genera Sapium and Sebatiana are strictly neotropical. The Malesian species will have to be transferred, Sebastiana to, for instance, Microstachys and Gymnanthes. Homalanthus should be Omalanthus. Excoecaria is correct.
Dr. R. Vajravelu will also join the project, just as Mr. B. Perumal and several staff members and MSc students of the Bogor herbarium in Indonesia. Their subjects of revision will be selected in the near future.
The Tree Flora of Sabah and Sarawak project has started recently. The revision of the Euphorbiaceae for these two Malayan states is scheduled to be finished in December 1998 and will be published in the third volume. Mr. Abang Mohtar, Dr. Jumaat Adam, and Mr. K.M. Kochummen will help to revise these W and N Bornean Euphorbs. Contributors to the Flora Malesiana project are kindly invited to extract the data of their tree species for the Tree Flora of Sabah and Sarawak. The format will be more or less equal to the Tree Flora of Malaysia, however, a special guide to contributors can be obtained: Chief Editor, Tree Flora of Sabah & Sarawak Project, Forest Research Institute of Malaysia, Kepong, 52109 Kuala Lumpur, Malaysia.
Adam, J. |
Tree Flora of Sabah & Sarawak Project, FRIM, Kepong, 52109 Kuala Lumpur, Malaysia |
Ahumada, L.Z. |
Herbarium Humboldtianum (CTESN), Facultad de Cincias Exactas y Naturales y Agrimensura, U.N.N.E., Casilla de Correo 326, 3400 Corrientes, Argentina |
Armbruster, W.S. |
Herbarium (ALA), University of Alaska Museum, Fairbanks, Alaska 99775-1200, U.S.A. |
Banka, R.A. |
PNG Forest Research Institute, Lae National Herbarium, P.O. Box 314, Lae, Papua New Guinea |
Bruhl, J. |
Herbarium (NE), Botany Department, University of New England Armidale, New South Wales 2351, Australia |
Brunel, J.F. |
Herbier (P), Laboratoire de Phanérogamie, Muséum National d'Histoire Naturelle, 16 rue Buffon, F-75005 Paris, France |
Carter, S. |
Herbarium (K), Royal Botanic Gardens Kew, Richmond, Surrey TW9 3AB, England |
Cordeiro, I. |
Herbário (SPF), Departamento de Botânica, Universidade de São Paulo, Caixa Postal 11461, 05499 São Paulo, Brasil |
Herbarium (HBG), Institut für Allgemeine Botanik, , Ohnhorststrasse 18, D-2000 Hamburg, Germany |
|
Fernandez Casas, J. |
Herbario (MA), Real Jardín Botánico, Plaza de Murilloz, 28014 Madrid, Spain |
Forster, P. |
Queensland Herbarium (BRI), Department of Primary Industries, Meiers Road, Indooroopilly, Queensland 4068, Australia |
Gilbert, M.G. |
Botany, The Natural History Museum, Cromwell Road, London SW7 5BD, Engeland. Flora of China project |
Gillespie, L.J. |
National Museum of Natural History, Botany Department, NHB-166 (US), Smithsonian Institution, Washington, D.C. 20560-0001, U.S.A. |
Henderson, R.J.F. |
Queensland Herbarium (BRI), Department of Primary Industries, Meiers Road, Indooroopilly, Queensland 4068, Australia |
Huft, M.J. |
Herbarium, Botany Department (F), Field Museum of Natural History, Roosevelt Road at Lake Shore Drive, Chicago, Illinois 60605-2496, U.S.A. |
Kochummen, K.M. |
Tree Flora of Sabah & Sarawak Project, FRIM, Kepong, 52109 Kuala Lumpur, Malaysia (died). |
Koutnik, D.L. |
6922 Hesperia Avenue, Reseda, CA 91335, U.S.A. |
Levin, G.A. |
Herbarium (SD), San Diego Natural History Museum, P.O. Box 1390 San Diego, California 92122-1390, U.S.A. |
McPherson, G. |
Herbarium (MO), Missouri Botanical Garden, P.O. Box 299 Saint Louis, Missouri 63166-0299, U.S.A. |
Mitra, R. L. |
Central National Herbarium (CAL), P.O. Botanic Garden, Howrah, Calcutta 711 103, West Bengal, India |
Mohtar, A. |
Tree Flora of Sabah & Sarawak Project, FRIM, Kepong, 52109 Kuala Lumpur, Malaysia |
Perumal, Balu |
Department of Botany, School of Plant Sciences, University of Reading Whiteknights P.O. Box 221, Reading RG6 2AS, England |
Radcliffe-Smith, A. |
Herbarium (K), Royal Botanic Gardens Kew, Richmond, Surrey TW9 3AB, England |
Schot, A. |
Rijksherbarium/Hortus Botanicus, Leiden University, P.O. Box 9514, 2300 RA Leiden, The Netherlands |
Herbarium (MHA), Main Botanical Garden, 127276 Moscow, Russia |
|
Herbarium, Department of Botany, Faculty of Biology, University of Hanoi, Thuong Dinh, Dong Da, Vietnam |
|
Thomson, B. |
Northern Territory Herbarium (NT), Conservation Commission of Northern Territory, P.O. Box 1046, Alice Springs, Northern Territory 0871, Australia |
Thulin, M. |
Botanical Museum (Fytoteket) (UPS), Uppsala university, P.O. Box 541, S-751 21 Uppsala, Sweden |
Vajravelu, R. |
Arboretum, University of Central Florida, Orlando, Florida 32816-0368, U.S.A. |
Webster, G.L. |
John M. Tucker Herbarium (DAV), Botany Department, University of California, Davis, California 95616, U.S.A. |
Welzen, P.C. van |
Rijksherbarium/Hortus Botanicus, Leiden University, P.O. Box 9514, 2300 RA Leiden, The Netherlands |
Whitmore, T.C. |
Department of Geography, University of Cambridge, Downing Place, Cambridge CB2 3EN, England |
A: Herbarium, Arnold Arboretum, Harvard University, Cambridge, Massachusetts 02138, U.S.A.
BM: Herbarium, Botany Department, The Natural History Museum, Cromwell Road, London SW7 5BD, England.
BO: Herbarium Bogoriense, Jalan Ir. H. Juanda 22, Bogor, Indonesia.
BRI: Queensland Herbarium, Department of Primary Industries, Meiers Road, Indooroopilly, Queensland 4068, Australia.
BRUN: Herbarium, Forestry Department, Bandar Seri Begawan, Brunei Darrusalam.
CANB: Australian National Herbarium, CSIRO, G.P.O. Box 1600, Canberra, ACT 2601, Australia.
K: Herbarium, Royal Botanic Gardens Kew, Richmond, Surrey TW9 3AB, England.
KEP: Herbarium, Forest Research Institute of Malaysia, P.O. Box 201, Kepong, 52109 Kuala Lumpur, Malaysia.
L: Rijksherbarium/Hortus Botanicus, Leiden University, P.O. Box 9514, 2300 RA Leiden, The Netherlands.
LAE: Papua New Guinea National Herbarium, Forest Research Institute, P.O. Box 314, Lae, Papua New Guinea.
NSW: National Herbarium of New South Wales, Royal Botanic Gardens, Mrs. Macquarie's Road, Sydney, New South Wales 2000, Australia.
NY: Herbarium, New York Botanical Garden, Bronx, New York 10458-5126, U.S.A.
P: Herbier, Laboratoire de Phanérogamie, Muséum National d'Histoire Naturelle, 16 rue Buffon, F-75005 Paris, France.
PNH: Philippine National Herbarium, National Museum, P.O. Box 2659, Manila, Philippines
SAN: Herbarium, Forest Research Centre, Forest Department, P.O. Box 1407, 90008 Sandakan, Sabah, Malaysia.
SAR: Forest Herbarium, Department of Forestry, 93660 Kuching, Sarawak, Malaysia.
SING: Herbarium, Parks and Recreation Department, Botanic Gardens, Cluny Road, Singapore 1025, Singapore.
US: United States National Herbarium, Botany Department, NHB-166, Smithsonian Institution, Washington, D.C. 20560-0001, U.S.A.
LEPIDOPETALUM
P.C. van Welzen
Lepidopetalum Blume, Rumphia 3 (1847) 171; Radlk., Bot. Jahrb. 56 (1920) 56; in Engl., Pflanzenr. 98 (1933) 1316; Reynolds, Fl. Austral. 25 (1985) 87. --- Type species: Lepidopetalum perrottetii (Cambess.) Blume.
Lachnopetalum Turcz., Bull. Soc. Nat. Mosc. 21 (1848) 571. --- Type species: Lachnopetalum glabrum Turcz. (= Lepidopetalum perrottetii (Cambess.) Blume).
Tree. Indumentum simple hairs only. Branchlets smooth to slightly grooved, sericeous when young. Leaves paripinnate, spirally arranged, pulvinate at base, without pseudostipules; petiolules present as pulvinus. Leaflets subopposite to opposite, basal ones ovate, upper ones elliptic (to obovate), slightly asymmetric, acroscopic side broader, thin, not punctate; base usually cuneate, asymmetric; margin entire, flat; apex acuminate to caudate, very apex usually rounded; both surfaces smooth, subglabrous except at least for the subsericeous basal part of the midrib, below (a few) glabrescent hair tufts as domatia; venation raised, especially below, nerves marginally looped, veins reticulate. Inflorescences ramiflorous to axillary to pseudoterminal, reduced thyrses with usually 3 cymules per node, tendrils absent; rachis (sub)sericeous; cymules basally dichasial to apically cincinnate, those with male flowers often with an exceptional number of sepals, petals, and stamens in first developed flowers. Bracts and bracteoles triangular to long triangular to at least a few leaf-like in L. subdichotomum, mainly margin and outside sericeous. Pedicels subglabrous to pilose, glandular hairs present besides simple ones; upper part above abcission zone less pilose to glabrous except for glandular hairs. Flowers actinomorphic. Sepals 5 (or 6), (sub)equal, basally united, apert; tube disc-shaped, c. 0.3 mm long; blades triangular (to ovate), mainly margin and outside pilose. Petals 5(--7); nail c. 0.1 mm high; blade triangular, margin only to completely pilose; scales united into one, occasionally still bifid, larger than blade, margin irregularly crenate, pilose; crests usually absent, sometimes present as central ridges or as 2 flat scales. Disc circular,complete to with often a few slits in L. xylocarpum, flat to high, smooth, glabrous, enveloping base of stamens, without rim or collar. Stamens (7--)8(--10); filaments especially basally pilose; anthers basifixed, laterally opening with lengthwise slits, pilose. Pistil: ovary flat, 2- (or very occasionally 3-)locular, smooth, subglabrous to hirsute; ovule one per locule; style and stigma united, flat, triangular, stigmatic part folded outwards like overhanging roof. Fruit an obovoid capsule, regularly dehiscing, with usually 1 developed seed, flat when 2-locular, coriaceous to woody, smooth to somewhat rough, outside glabrous, margin sharp, almost slightly winged to blunt, inside glabrous to short to long brownish pilose, without extra fleshy layer; stipe absent to present; wall thin, at most 2 mm thick. Seed ellipsoid, triangular in transverse view, base straight to oblique, smooth, shiny; sarcotesta glabrous, covering seed only basally to almost completely except for a small triangular dorsal area; testa thin, without radicle pocket on the inside. Embryo: cotyledons laterally to secondarily laterally besides each other, equal to inequal, then upper much larger, apices not elongated; radicle present basally to about halfway seed, short; plumule inconspicuous.
Field notes -- Bark greyish brown, slightly fissured and/or with lenticels. Flowers yellowish white. Fruit red; sarcotesta orange; seed black.
Distribution -- 6 Species from India (Andaman and Nicobar Isl.; 1 non-endemic species) to NE Australia and the Solomon Islands (also 1 non-endemic species each); all species occurring in Malesia:, mainly endemic.
Ecology -- Trees in primary and secondary forest, on waste land, along rivers and roads. Alt.: sealevel up to 1200 m. Flowering and fruiting: different per species, variable between seasonal and whole year through.
Note -- The phylogeny and historical biogeographical pattern of Lepidopetalum is described in Van Welzen (1992).
Key to the species of Lepidopetalum based on flowering characters
Caution: the differences in floral characters among the species are only slight. Therefore, geography is used as an additional 'character'; however, due to insufficient collecting, the geographical ranges of some species may be larger than described in the key.
1a. |
Upper part of pedicels pilose. |
|
1b. |
Upper part of pedicels glabrous except for glandular hairs. |
|
2a. |
Disc as high as broad or broader than high (flat). Philippines, New Guinea, Solomons. |
|
2b. |
Disc higher than broad. Nicobar Is, Sumatra. |
3. L. montanum |
3a. |
Ovary (sub)glabrous (to pilose); if pilose then disc usually with slits. Petals 0.5--2.2 mm high, crests often present as ribs or as flat scales. New Guinea and the Solomons. |
|
3b. |
Ovary pilose; disc without slits. Petals 0.4--1 mm high, crests absent. Philippines. |
|
4a. |
Disc as high as broad, without slits. Crests usually present on petal scales as ribs or as flat scales. Ovary (sub)glabrous. N coast New Guinea: E Geelvink Bay to Madang Prov. |
2. L. micans
|
4b. |
Disc flat to as high as broad, usually with slits. Crests usually absent, at most present as ribs. Ovary subglabrous to pilose. New Guinea: Peninsula to S coast to Vogelkop. |
6. L. xylocarpum |
5a. |
Stamens 8, some flowers (of a cymule especially the firest flowering male ones) with 9 or more. Solomons and New Guinea (absent in Morobe Prov.). |
|
5b. |
Stamens 8. New Guinea: Morobe Prov. |
1. L. fructoglabrum |
6a. |
Inflorescences up to 17 cm long, axillary to pseudoterminal. Per inflorescence at least a few big bracts; bracts 1--3.3 mm long. Solomons and N New Guinea: Jayapura to Morobe Prov. to Bougainville. |
5. L. subdichotomum |
6b. |
Inflorescences up to 8.5 cm long, usually ramiflorous on thin twigs to axillary to pseudoterminal. Per inflorescence only small bracts; latter 0.7--1.3 mm long. New Guinea: Peninsula to S coast to Vogelkop. |
6. L. xylocarpum |
Key to the species of Lepidopetalum based on fruit characters
1.a. |
Fruit inside pilose. |
|
1.b. |
Fruit inside glabrous. |
1. L. fructoglabrum |
2.a. |
Sarcotesta only basally present around hilum. |
|
2.b. |
Sarcotesta covering seed except for (part of) dorsal side. |
|
3.a. |
Upper part pedicels sericeous. Sarcotesta with well-developed basal obpyramidal outgrowth. |
|
3.b. |
Upper part pedicels glabrous. Sarcotesta with slight basal obpyramidal outgrowth. |
5. L. subdichotomum |
4.a. |
Fruit 3.2--4.5 cm high by 1.7--2.4 cm broad. |
3. L. montanum |
4.b. |
Fruit 1.3--2.5 cm high by 0.8--1.6 cm broad. |
|
5.a. |
Fruit inside long pilose (hairs c. 1.5 mm long). Sarcotesta covering seed except for small dorsal triangular part. |
2. L. micans |
5.b. |
Fruit inside short pilose (hairs c. 0.5 mm long). Sarcotesta covering seed except for dorsal side. |
6. L. xylocarpum |
4. Lepidopetalum perrottetii (Cambess.) Blume, Rumphia 3 (1847) 172; Miq., Fl. Ned. Ind. 1, 2 (1859) 569; Radlk., Sap. Holl.-Ind. (1879) 15, 46, 92; Sitzungsber. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. München 9 (1879) 535, 622; Radlk. in Engl., Pflanzenr. 98 (1933) 1317. -- Cupania perrottetii Cambess., Mém. Mus. Hist. Nat. Paris 18 (1829) 45. --- Type: Perrottet s.n. (P, holo; iso in L, P), Philippines, Samboanga (= Zamboanga), not Manila.
Lachnopetalum glabrum Turcz., Bull. Soc. Nat. Moscou 21 (1848) 572; Miq., Fl. Ind. Bat. 1, 2 (1859) 557. -- Ratonia lachnopetala Turcz., Bull. Soc. Nat. Moscou 36 (1863, n.v.) 586, nom. illeg. (ICBN art. 63.1). --- Type: Cuming 1169 (holo unknown; iso in L, M, MEL, NY, P), Philippines, Luzon, South Ilocos Prov.
Cupania ? richii A. Gray, U.S. Expl. Exp. Bot. 1 (1854) 257; Merr., Philip. J. Sc. 3 (1908) 79. --- Type: U.S. Expl. Exp. (A, holo), Philippines, Mindanao, Caldera.
Flowering branchlets 3--5 mm in diam. Leaves 2--4-jugate; rachis 1.6--17.3 cm long, terete, (sub)sericeous. Leaflets 2.5--24 by 1.2--10 cm; apex acuminate, very apex emarginate to usually rounded. Inflorescences axillary with a tendency towards ramiflory, branching mainly in axil or along rachis, latter up to 7 cm long. Bracts and bracteoles triangular to long triangular; bracts 1.1--2 mm long; bracteoles 0.6--1 mm long. Pedicels sericeous, upper part 2--8 mm long. Flowers c. 4 mm in diam. Sepals 5 (or 6); blades 0.8--2.3 by 0.6--1.5 mm, mainly outside sericeous. Petals 5; blade triangular, 0.4--1 by 1--1.6 mm, completely pilose; scale 0.8--1.7 by 1.2--1.8 mm; crests absent. Disc complete, c. 0.4 mm high, broader than high. Stamens 8; filament in male flowers 1.2--3.3 mm long, in female flowers 0.4--1.8 mm; anther in male flowers 0.6--0.9 by 0.5--0.8 mm, in female flowers 0.4--0.7 by 0.5--0.8 mm. Pistil: ovary in male flowers 0.3--0.4 mm high, in female flowers 1.8--2.5 mm high, 2-locular, hirsute; style and stigma in male flowers 0.05--0.1 mm long, in female flowers 0.9--1.8 mm long. Fruit 1.3--2.5 by 0.8--1.6 cm, inside densely hirsute with hairs c. 0.5 mm short; stipe absent (to 2 mm high). Seed 6--12 by 5--9.5 mm, base oblique; sarcotesta covering seed at base, present around hilum, forming obpyramidal outgrowth below seed; hilum 0.8--1.1 mm long. Embryo 6.5--9.5 by 6.5--8 mm; cotyledons obliquely dorsoventrally above each other; radicle up to 1.3 mm long.
Field notes -- Shrub to tree, 2--17 m high, d.b.h. 6--25 cm. Flowers cream, Fruit red; sarcotesta yellow; seed black.
Distribution -- Malesia: Philippines (mainly E and N).
Ecology -- Found along roadsides, in secondary forest, on waste land, and along forest edges. Alt.: sea level up to 1200 m. Probably two flowering seasons: Jan. to March (to April) and May to June. Fruiting: (Feb. to) March to June and Sept. to Nov. (to Feb.).
Note -- Clinal variation exists from Mindanao to Luzon, the leaflets and fruits decrease in size.