REINWARDTIA_13-2_7Oct2010


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IN

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13 (2) 

A JOURNAL ON TAXONOMIC BOTANY,  
PLANT SOCIOLOGY AND ECOLOGY  

ISSN 0034 – 365 X 



REINWARDTIA  
 
A JOURNAL ON TAXONOMIC BOTANY   
PLANT SOCIOLOGY AND ECOLOGY  
 
Vol.  13(2):  95 — 220,  November 2,   2010 
 
Chief Editor 
KARTINI KRAMADIBRATA 

 

Editors 
DEDY DARNAEDI 
TUKIRIN PARTOMIHARDJO 
JOENI SETIJO RAHAJOE 
TEGUH TRIONO  
MARLINA ARDIYANI  
EIZI SUZUKI 
JUN WEN 
 
Managing editors 
ELIZABETH A. WIDJAJA 
HIMMAH RUSTIAMI 
 
Secretary 
ENDANG TRI UTAMI 
 
Lay out 
DEDEN SUMIRAT HIDAYAT 
 
Ilustrators 
SUBARI 
WAHYU SANTOSO 
ANNE KUSUMAWATY 
 
Reviewers 
R. ABDULHADI, SANDY ATKINS, JULIE F. BARCELONA, TODD  J. BARKMAN,  NICO CELLINESE,   MARK 
COODE, GUDRUN KADEREIT,  ROGIER DE KOCK, N. FUKUOKA,  KUSWATA KARTAWINATA, ARY P. KEIM, P. 
J. A. KESSLER, A. LATIFF–MOHAMAD,  M. A. RIFAI,  RUGAYAH,  H. SOEDJITO, T. SETYAWATI, D. G. STONE, 
WAYNE TAKEUCHI,  BENITO C. TAN, J. F. VELDKAMP, P. VAN WELZEN, H. WIRIADINATA, RUI-LIANG ZHU. 
 
 
Correspondence on editorial matters and subscriptions for Reinwardtia should be addressed to: 
HERBARIUM BOGORIENSE, BOTANY DIVISION, 
RESEARCH CENTER FOR BIOLOGY– LIPI, 
CIBINONG 16911, INDONESIA 
Email: reinwardtia@mail.lipi.go.id 



REINWARDTIA 
Vol 13, No 2, pp: 213  − 220 

213 

MARANTACEAE IN SULAWESI 
Received July 19, 2010; accepted September 17, 2010 
 
M. ARDIYANI 
Herbarium Bogoriense, Research Centre for Biology – LIPI , Jl. Raya Jakarta-Bogor km.46,  
Cibinong 16912, Indonesia. E-mail: marlina.ardiyani@gmail.com 
 
A. D. POULSEN  
Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh EH3 5LR, Scotland, UK. 
 
P. SUKSATHAN 
Herbarium, Queen Sirikit Botanic Garden, P.O. Box 7, Mae Rim, Chiang Mai 50180, Thailand. 
 
F. BORCHSENIUS 
Department of Biological Sciences, Ecoinformatics and Biodiversity, Aarhus University, Ny Munkegade, Building 1540, 
DK-8000 Aarhus C, Denmark 
 
 
ABSTRACT 
ARDIYANI, M., POULSEN, A. D., SUKSATHAN, P., BORCHSENIUS, F. 2010. Marantaceae in Sulawesi. 
Reinwardtia 13(2): 213–220.  — Six species of Marantaceae occur in Sulawesi. We present a key to the species 
together with a taxonomic treatment with notes on species delimitation, distribution, habitat and ecology, vernacular 
names and uses. One species endemic to Sulawesi and not covered by any contemporary publication, Phrynium 
longispicum (Warb. ex K. Schum.) Suksathan & Borchs. is described and neotypified. Donax canniformis (G. Forst.) K. 
Schum., Phrynium pubinerve Blume, Phrynium robinsonii (Valeton) Suksathan & Borchs, Stachyphrynium latifolium 
(Blume) K. Schum. and Stachyphrynium repens (Körn.) Suksathan & Borchs. are also reported from Sulawesi and 
characterized. For the two last species these occurrences represents an extension of their previously known range across 
Wallace's line. 
 
Key words: Donax, ethnobotany, neotypification, Phacelophrynium, Phrynium, Stachyphrynium, Sulawesi, Wallace’s 
line 
 

ABSTRAK 
ARDIYANI, M., POULSEN, A. D., SUKSATHAN, P., BORCHSENIUS, F. 2010. Marantaceae di Sulawesi. 
Reinwardtia 13(2): 213–220. — Enam jenis dari suku Marantaceae terdapat di Sulawesi. Disajikan kunci  ke jenis 
beserta perlakuan taksonominya. Satu jenis merupakan endemik di Sulawesi yang belum pernah ada dalam publikasi 
kontemporer sebelumnya, Phrynium longispicum (Warb. ex K. Schum.) Suksathan & Borchs. dideskripsikan dan 
dineotipifikasi. Donax canniformis (G. Forst.) K. Schum., Phrynium pubinerve Bl., Phrynium robinsonii (Valeton) 
Suksathan & Borchs, Stachyphrynium latifolium (Blume) K. Schum. dan Stachyphrynium repens (Körn.) Suksathan & 
Borchs. juga dilaporkan dari Sulawesi dan dikarakterisasi. Keberadaan dua jenis terakhir melampaui distribusi yang 
sebelumnya hanya diketahui di timur garis Wallace.   
 
Kata kunci: Donax, etnobotani, neotipifikasi, Phacelophrynium, Phrynium, Stachyphrynium, Sulawesi, garis Wallace. 

INTRODUCTION 
 

The Marantaceae includes about 23 genera and 
550 species worldwide (Andersson, 1998). Eight 
genera and an estimated 55 species occur in tropical 
Asia (Suksathan et al., 2009). Over the last few 
years, several publications have helped clarify the 
taxonomy of the West Malesian species (Clausager 
& Borchsenius, 2003; Suksathan & Borchsenius, 
2003, 2005, 2008; Poulsen & Clausager, 2004; 
Clausager et al., 2006; Suksathan et al., 2006, 
2010), but the Marantaceae occurring east of 
Wallace's line are still very poorly documented.  

Prior to our recent fieldwork, the most recent 
account of the Marantaceae of Sulawesi was by 
Koorders (1898) who, in his account of the flora of 
north Sulawesi, listed three species: Maranta 
dichotoma Wall. [a synonym of Schumannianthus 
dichotomus (Roxb.) Gagnep. misapplied to Donax 
canniformis (G. Forst.) K. Schum.]; Maranta indica 
Tussac [a synonym of the widely cultivated root 
crop M. arundinacea L.] and Phrynium capitatum 
[a synonym of P. pubinerve Blume which is 
probably a misidentification of P. longispicum].  

In this paper we provide a taxonomic account of 
the Marantaceae of Sulawesi. The data presented 



  REINWARDTIA  214                                [VOL.13 

are based on field work carried out in 2008 and 
2009 and examination of herbarium specimens 
found at AAU, BO, E, L and S.  The endemic 
Phrynium longispicum (Valeton) Suksathan & 
Borchs., for which no up-to-date description exists, 
is described in full and neotypified. For the 
remaining five species which are already covered 
by detailed descriptions in the literature we provide 
only a brief characterization. Generic delimitation 
follows Suksathan et al. (2009). Descriptive 
terminology regarding inflorescence structure 
follows Clausager & Borchsenius (2003). The term 
'special paraclade' refers to the basic flower-bearing 
structure of the inflorescence while 'fertile bracts' 
refer to those bracts that subtend a special 
paraclade. 
 
Key to the species of Marantaceae in Sulawesi 
1. a. Shrub-like plants with a tall and richly branched 

aerial stem. Fruit fleshy, indehiscent......................... 
 ....................................................Donax canniformis 
    b. Rosulate plants with short, unbranched aerial stems 

arising from the rhizome. Fruit dry, capsular..........2 
2. a. Sepals less than 1/5 of the corolla tube 

[Stachyphrynium]....................................................3 
 b. Sepals more than 1/3 of the corolla tube 

[Phrynium]..............................................................4 
3. a. Inflorescence borne on a separate, leafless shoot; 

leaf blade 40–85 cm long........................................ 
 ........................................Stachyphrynium latifolium 
  b. Inflorescence interfoliar; leaf blade 10–20 cm long.. 
     ..............................................Stachyphrynium repens 
4. a.  Fruit red. Inflorescence capitate. Two outer 

staminodes................................Phrynium pubinerve 
     b. Fruit green or brown. Inflorescence branches clear-

ly discernible. One outer staminode........................5 
5. a. Flower up to 40-50 mm long. Inflorescence with 1–

3 basal branches arising in the same point, each with 
several fasciculate, flower bearing branches 
separated by very short internodes............................. 

 ............................................Phrynium longispicatum 
     b. Flower up to 25 mm long. Inflorescence with seve-

ral lateral branches, separated in the proximal part 
by internodes up to 6.5 cm long................................ 

  ..................................................Phrynium robinsonii 
 
 
1. DONAX CANNIFORMIS (G. Forst.) K. Schum. 
 

Donax canniformis (G. Forst.) K. Schum., Bot. Jahrb. 
Syst. 15(4): 440. (1893). — Thalia canniformis G. Forst., 
Fl. Ins. Austr.: 1 (1780). Type: The New Hebrides 
(Vanuatu islands) J.G.A. Forster s.n. (Holotype BM!).  

Donax grandis (Miq.) Ridl., J. Straits Branch Roy. 
Asiat. Soc. 32: 176. 1899. For a full nomenclatural 
account see Suksathan & Borchsenius (2005). 
 

Upright herb with a richly branched stem, to 5 m 
tall. Leaves clustered towards the ends of the 

branches; lamina 8–30x4–20 cm. Inflorescences 
several on each plant, each to 30 cm long, richly 
branched, lax, composed of up to 15 major branches 
of increasing orders (usually 2–5 branches in 
Sulawesi plants). Special paraclade markedly 
elongate, primary axis 25–30 mm long 
(dolichoblastic), with 1–2 flower pairs; pedicel of 
individual flowers 5–25 mm long, each with an 
associated small glandular bracteole that functions 
as a nectary to attract ants that protect flowers and 
developing fruits against herbivores. Flower white 
to yellowish white, ca. 15 mm long; corolla tube ca. 
5 mm long; staminal tube ca. 2 mm longer than 
corolla tube. Fruit white or greenish cream and 
fleshy at maturity, green while immature, 
indehiscent, smooth and globose, ca. 1–1.4 cm in 
diameter; seeds 1–3, black. 
 
Distribution. Widespread and common throughout 
S. E Asia, from India to the Solomon Islands and 
Vanuatu and northwards to Orchid Island (Taiwan) 
 
Habitat and ecology. Primary and secondary 
lowland  rainforest, on hillslopes, rockbeds along 
small streams and wet areas such as alluvial 
flatland. Common, especially in open and disturbed 
places. 
 
Vernacular Names. Moah, Moha (Minahassa, 
Sangir language) (Poulsen et al. 2602; Koorders 
19681ß); Bomban (Mongondouw) (Arifiani et al. 
377; Wardi 020); Bawambanan’a (Talaud) (H.J. 
Lam 3061); Neue (Kobaena) (Widjaja 771); Nena 
(Buton) (Uji 4686); Beeo (Buton) (Widjaja 568); 
Elusan im bolai (Tontemboan or Tompakewa 
language; Koorders 1898); Nelusan ing kawok 
(Tulur language; Koorders 1898); Tuis in talun 
(Tontemboan or Tompakewa language; Koorders 
1898); Mundung (Tulur language; Koorders 1898). 
 
Uses. For making mats (Poulsen et al. 2602). Stem 
used as string (Widjaja 771). Short lengths of rattan
-like cane can be obtained from the green outer 
layer of the internodes (Coode 6066). Medicinal 
plants (precise usage not specified - Uji 4686). 
Inner young shoot is grated then squeezed, taken 
internally to treat high fever (Arifiani et al. 377).  
Used to climb Metroxylon; for making fish traps; 
and young stems used against skin rashes (Koorders 
1898 – as Maranta dichotoma). 
 
Notes. Full botanical descriptions of Donax 
canniformis in Borneo and Thailand, respectively, 
can be found in Clausager & Borchsenius (2003) 
and Suksathan & Borchsenius (2008). 
 



2010]                      215   ARDIYANI et al.: Marantaceae in Sulawesi 

Specimens seen from Sulawesi. North Sulawesi. Dua 
Saudara Nature Reserve, Temboan, 6 km S of Batu Puteh 
village, small valley in forest (1°31'13''N, 125°08'21''E), 
350 m, 14 February 2008, fruiting, Poulsen, Ardiyani, & 
Porawouw 2602 (AAU, BO, E); Mauk Molotong, along 
Mauk river (0°42'02.7''N, 124°02'36.3''E), 300–350 m, 
22 May 2002, flowering and fruiting, Arifiani, Nurdin,  
Lepinus & Marselak 337 (BO); Manado, no date, 
flowering, Riedel 5903 (BO); Bogani Nani Wartabone 
National Park, Toraut, April 2004, fruiting, Nurdin 35 
(BO); Menado, o. afd. Poso. Tusschen, 1 September 
1938, flowering and fruiting, Eyma 3513 (BO, L); 
Bolaang Mongondouw, Dumoga Bone National Park, 
Toraut Dam (0°34'N, 123°54'E), 220 m, 23 March 1985, 
fruiting, Vogel & Vermeulen 6697 (BO, L); Menado, 
Oetan aris, 10 m, 28 December 1894, flowering and 
fruiting, Koorders 19681ß (BO); Menado, oerwand by 
bivak Pinamvrangan naarby Kajoewatoe, 500 m, 4 
March 1895, flowering and fruiting, Koorders 19683ß 
(BO); Sangir and Talaud Islands, Talaud, Salibabu, S.E. 
slope of Ajambana Mountain, 180 m, 20 May 1926, 
flowering, Lam 3061 (BO); Gorontalo. Riedel s.n. (BO); 
Kec. Suwawa, Desa Tulabolo, Motomboto, 400 m, 24 
December 1994, fruiting, Afriastini & Rohajawati 2900 
(BO); Central Sulawesi. Balukang, Desa Siboang, 
Dusun Maros, near Kampung Sipatoh (0°28'59''S, 120°
06'25''E), 197 m, 24 July 2002, fruiting, Brown, Craven, 
Juswara & Ramadhanil 118 (BO, CEB); Palolo, 
Kamarora, forest garden behind Lore Lindu National 
Park fieldstation (1°15'S, 120°13'E), 700 m, 22 March 
2001, fruiting, Kessler et al. PK 3072 (BO, CEB); 
Kabupaten Luwu, Desa Teromu, Farhumpenai, 350 m, 
17 February 1986, fruiting, Wardi Wd. 020 (BO); South 
Sulawesi. South West Peninsula, NE of Makassar within 
54–60 km on the road (5°01'S, 119°35'E), 3 July 1976, 
fruiting, Meijer, W. 10718 (BO); 3–5 km W of Soroako 
(2°15–3°'S, 121°–121°45'E), 450 m, 15 July 1979, 
flowering and fruiting, Balgooy  et al. 4028 (BO, L); 
Bantimurung National Park, Kassekebo. Alluvial area 
below limestone cliffs (5°0'44.6''S, 119°41'16.7''E), 65 
m, 22 January 2009, flowering and fruiting, Poulsen, 
Ardiyani, Firdaus, Iqbal, Tigor & Mia 2760 (AAU, BO, 
CEB, E); Southeast Sulawesi. District Kolaka, 
Subdistrict Uluiwoi, village Sanggona, near Hutumolae, 
base of Gunong Pondunaa in Mount Watu Wila (3°
46.448'S, 121°39.226'E), 175 m, 12 May 2008, flowering 
and fruiting, Wen, & Kartonegoro 10196 (BO); Buton 
Island, Lawo-lawo area, Wakunti forest, Bau-bau, 26 
June 1978, fruiting, Widjaja 568 (BO); Kobaena Island, 
Enano, Matansolonsa Mountain, 5 July 1978, fruiting, 
Widjaja 771 (BO); Kolaka, Poli-polia, Pangi-pangi, 100 
m, 24 October 1978, flowering and fruiting, 
Prawiroatmodjo & Maskuri 1537 (BO, L); Kendari, 
Kabupaten Unaha, Sampara, Atolanu Mountain, 70 m, 6 
February 1986, flowering and fruiting, Amir 65 (BO); 
Buton Island, Kaboengka, 180 m, 15 February 1929, 
fruiting, Kjellberg 246 (BO, L); Kolaka area, Watuwila 
foothills, above Sanggona, “Mokuwu camp”, forest in 
valley of Mokowu R. (3°48'S, 121°39'E), 200 m, 29 
October 1989, flowering and fruiting, Coode 6066 (BO, 
L, K); Buton Island, North Buton Game Reserve, 
Maligano-Ronta km. 12 (4°42'04''S, 122°55'18''E), 200 

m, 27 April 2003, flowering and fruiting, Uji 4686 (BO). 
 
2. PHRYNIUM LONGISPICUM (Warb. ex K. 
Schum.) Suksathan & Borchs. 
 

Phrynium longispicum (Warb. ex K. Schum.) 
Suksathan & Borchs., Bot. J. Linn. Soc. 159: 394 (2009). 
— Phacelophrynium longispica Warb. ex K. Schum., in 
Engler, Pflanzenr. 4(48): 122 (1902). Type: Celebes, 
Northern Minahassa Peninsula, Boyong, Warburg, O. 
15739 (B destroyed, Syntype);  Celebes, Tomohon, June 
1894, Sarasin, K.F. & Sarasin, P. 411 (B destroyed); 
Northern Minahasa Peninsula, along trail from Boyong 
Atas village to Gunung Lolombulan (1°5'18.3''N, 124°
25'23.2''E), 700 m, 24 February 2009, flowering and 
fruiting, Poulsen, A. D., Kinho, J., Sandaling, T. & 
Mandei, N. 2815 (Holoneotype BO!, Isoneotypes AAU!, 
E!, SING!). — Fig 1. 
 

Rosulate, clustering herb, to 1.5 m tall. Leaves (1
–) 4–5 on each shoot; petiole to 135 cm long; 
pulvinus 3.5–7.5 cm long, yellowish green; leaf 
blade 27–52x15–22 cm. Inflorescence borne among 
the leaves, terminal on a 25–55 cm tall stem with a 
node ca. 3 cm below the base of the inflorescence, 
the node supporting a small leaf or a short bladeless 
sheath; inflorescence 14–18 cm tall, at first almost 
spicate, in later stages with 1–3 basal branches, each 
with up to 10 clustered, flower-bearing branches, 3–
15 cm long; sterile basal bracts to 8 cm long; fertile 
bracts 30–35 mm long, to 20 mm wide, rolled into a 
tubular structure; special paraclade with a single 
flower-pair, associated prophyll 22x7 mm. Flowers 
white to yellowish white, 40–50 mm long; sepals 9–
10 mm long, narrow, ca. 1 mm wide in distal 1/3; 
corolla tube 16–20 mm long, lobes 16–17x3–5 mm, 
dark pigmented in longitudinal stripes in distal 1/3; 
staminodal tube ca. 7 mm longer than corolla tube; 
outer staminode 1, petaloid lobe ca. 12x6 mm; 
callose staminode with petaloid lobe ca. 8x7 mm, 
bifid; cucullate staminode ca. 5 mm long; fertile 
stamen 6 mm long, theca ca. 2x1 mm. Fruit green 
(immature), rounded-triangular in cross-section, 9x7 
mm, with scattered white simple hairs; pedicel ca. 3 
mm long; seeds 3, angular, rugose, 6x4 mm; aril 
white (immature), bilobed. 
 
Distribution. Endemic to Sulawesi. 
 
Habitat and ecology. In disturbed primary forest 
and swampy forest. Alluvial flat land to lower hill 
slopes. Recorded up to 1,075 m elevation. 
 
Vernacular name. Polipot (Uji 4496). 
 
Uses. Ornamental plants (Uji 4496). 
 
Notes. Both syntypes cited in the original 



  REINWARDTIA  216                                [VOL.13 

description of the species are lost. As neotype we 
have chosen a recent collection with both flower 
material in alcohol and fruits (Poulsen et al. 2815) 
from Boyong; the same locality as one of the 
syntypes, Warburg 15739. This neotype well agree 
with the protologue of the species. Phrynium 
longispicum was included in the phylogenetic study 
by Suksathan and Borchsenius (2009) under the 
accession name Phacelophrynium sp. 1 (DNA 
extracted from the specimen Vogel & Vermeulen 
6721, L). The results show that P. longispicum is 
more closely related to Philippine taxa such as 

Phrynium interruptum than to the New Guinea 
clade of Phrynium (including species such as P. 
giganteum, P. kaniense and P. macrocephalum). 
 
Specimens seen from Sulawesi (other than the 
neotype). North Sulawesi. Gunung Masarang. 
Secondary forest (1°19'33''N, 124°52'6''E), 1,075 m, 20 
February 2008, flowering and fruiting, Poulsen, Ardiyani 
& Kaunang 2624 (AAU, BO, E); Bogani Nani 
Wartabone National Park, Mount Simbalang, 800 m, 20 
May 2002, flowering, Uji 4496 (BO); Bolaang 
Mongondouw, Dumoga Bone National Park, Toraut Dam 

Fig. 1.  Phrynium longispicum (Warb. ex K. Schum.) Suksathan & Borchs. Photograph of Poulsen et al. 2815 (the 
neotype) by A.D. Poulsen. 



2010]                      217   ARDIYANI et al.: Marantaceae in Sulawesi 

(0°34'N, 123°54'E), 220 m, 25 March 1985, flowering 
and fruiting, Vogel & Vermeulen 6721 (BO, L); 
Minahasa (Menado), 1896, Koorders & Valeton 19686ß 
(BO); Manado, Tonsealama, 700 m, 4 December 1932, 
flowering, Wisse 53 (BO); Along trail from Boyong Atas 
village to Gunung Lolombulan (1°5'18.3''N, 124°
25'23.2''E), 700 m, 24 February 2009, flowering and 
fruiting, Poulsen, Kinho, Sandanling & Mandei 2815 
(AAU, BO, E, SING); Gurupahi, 18 Mar 1917, 
flowering, Kaudern 25 (S); Central Sulawesi. Area of 
Mt. Nokilalaki, Paliti by Lake Lindu (1°13'S, 120°08'E), 
970 m, 2 May 1975, flowering, Meijer 9960 (BO) Forest 
patch near trial in garden area (0°59'20.2''N, 121°
36'4.3''E), 50 m, 22 February 2009, flowering, Poulsen & 
Kinho 2810 (AAU, BO, E).  
 
3. PHRYNIUM PUBINERVE Blume 
 

Phrynium pubinerve Blume, Enum. Pl. Javae: 38 
(1827). Type: Indonesia, Java, Blume s.n. (Holotype L!). 

Phrynium capitatum Willd., Sp. Pl. 1: 17. 1797 
(illegitimate name based on the same type as Pontederia 
ovata L.). 

Phrynium rheedei Suresh & Nicolson in Taxon 35: 
355. 1986. 

Phrynium malaccense Ridl., J. Straits Branch Roy 
Asiat. Soc. 32: 180. 1899.  

Phrynium philippinense Ridl., Leafl. Philipp. Bot. 2: 
570. 1909.  

Phrynium pubigerum Blume, Enum. Pl. Javae: 37. 
1827., For a full nomenclatural account see Suksathan & 
Borchsenius (2005). 
 

Rosulate herb, 0.7–3.5 m tall. Leaves 2–3 per 
shoot; lamina 23–82 × 9–30 cm, glabrous except for 
small hairs around the midrib. Inflorescence 
terminal on a leafy shoot, erect, usually appearing to 
protrude from the petiole of an accompanying leaf, 
capitate, 4–8 cm in diameter; bracts sheathing the 
inflorescence quickly withering apically and 
dissolving into a decaying fibrous mesh; flower 
pairs 2–4 per special paraclade. Flowers pinkish 
white, ca. 1.8 cm long; sepals ca 10 mm long; 
corolla tube 4–5 mm long; outer staminodes 2, their 
petaloid lobes 3–4.5 mm long. Fruits bright red, 
elongate to triangular, ca 15 × 10 mm, dehiscent; 
seeds 3, grey, with a small aril. 
 
Distribution. Widely distributed in SE Asia, from 
India to Burma, Thailand, Laos, Vietnam, 
Cambodia, Peninsular Malaysia, Sumatra, Java, 
Borneo, the Philippines and New Guinea. 
 
Habitat and ecology. This species seems to prefer 
a moderate level of habitat disturbance, and is often 
found growing next to streams, roads and trails, or 
even in the understorey of old rubber plantations. 
 
Vernacular name. Onese (Tolaki language) (A.D. 

Poulsen et al. 2791). 
 
Uses. Juice from the stem is used to cure irritant 
eyes; the stem is used for weaving or to keep roof 
thatching in place (Poulsen et al. 2791). 
 
Notes.  A widespread and variable species found 
throughout SE Asia. It is recognized by the 
combination of red fruits, capitate inflorescence 
with tattering inflorescence bracts, and flowers with 
two outer staminodes. Taxonomic treatments for 
Borneo and Thailand, with full botanical 
descriptions, are provided by Clausager and 
Borchsenius (2003) and Suksathan & Borchsenius 
(2008), respectively. Herbarium material of this 
species is often identified as Phrynium capitatum 
Willd. which, however, is an illegitimate name 
synonymous with P. pubinerve (see Clausager & 
Borchsenius 2003). 
 
Specimens seen from Sulawesi. Southeast Sulawesi. 
Selayar, s.d., flowering and fruiting, Teysmann 13605 
(BO); Boroboro range, N. of Wolasi. 16 km S of Kendari 
(4°9'14.6''S, 122°29'38.2''E), 180 m, 11 February 2009, 
flowering and fruiting, Poulsen, Ardiyani, Chahyadi & 
Gufrin 2791 (AAU, BO, E, QBG). 
 
4. PHRYNIUM ROBINSONII (Valeton) Suksathan 
& Borchs. 
 

Phrynium robinsonii (Valeton) Suksathan & Borchs.,  
Bot. J. Linn. Soc. 159: 394 (2009). — Phacelophrynium 
robinsonii Valeton, in Merrill, Interpr. Rumph. Herb. 
Amboin.: 166 (1917). Type: Indonesia, Ambon, Mahija, 
7 August 1913, along small stream, ca. 250 m alt., 
Specimen labeled "Robinson Plantae Rumphianae 
Amboinenses No. 521" (Holotype BO!).  —  Fig 2. 
 

Herb, to 2 m tall. Fertile shoots with 15–45 cm 
tall stem. Sheath of basal leaf ca. 120 cm long, 
petiole 10 cm long, blade 40–50x17–25 cm. 
Inflorescence with peduncle 10–20 mm long 
measured from node of subtending leaf, primary 
inflorescence branches 2–4, the proximal ones 
separated by internodes of 30–65 mm long. Primary 
bracts to 25 mm long, persisting. Flower pairs 2–3 
per special paraclade. Flowers to 25 mm long; 
sepals ca. 7 mm long; corolla tube ca. 16 mm long, 
petal lobes elongate, 10–12 mm long; outer 
staminode 1, linear, ca. 7 mm long; callose 
staminode with an elliptic, emarginate petaloid lobe, 
ca. 6 mm long. Fruit ca. 10x5 mm; seeds 1(–2). 
 
Distribution. Endemic to the Moluccas and 
Sulawesi. 
 
Habitat and ecology. Not much is known, but it 



  REINWARDTIA  218                                [VOL.13 

seems to occur mostly at low elevations. 
 
Notes. This species is known from several 
collections in the Moluccas and a single record from 
Sulawesi. We have not found this species in the 
field and we have had no access to fresh or pickled 
flower material. The above description of flowers is 
based on Valeton's (1917) protologue. According to 
Valeton, the flowers of P. robinsonii are markedly 
smaller (25 mm long) than those of P. longispicum 
(ca. 40 mm long). The inflorescence structure also 
seems to be different in the two species, more 
elongate and with fewer branches per node in P. 
robinsonii. The limit between the two species 
should, however, be reinvestigated as more material 
becomes available. 

Specimens seen from Sulawesi. Palopo, Bulong, sea 
level, 28 February 1929 Kjellberg 1996 (BO, S). 
 
5. STACHYPHRYNIUM LATIFOLIUM (Blume) 
K. Schum. 
 

Stachyphrynium latifolium (Blume) K. Schum., in 
Engler, Pflanzenr. IV. 48 (Heft 11): 49 (1902). — 
Phrynium latifolium Blume, Enum. pl. Javae : 37 (1827). 
Type: Indonesia, Java, Bantam province, Blume s.n. 
(holotype L!).  

Stachyphrynium cylindricum (Ridl.) K. Schum., in 
Engler, Pflanzenr. 4(48): 49. 1902. 

Stachyphrynium griffithii (Baker) K. Schum., in 
Engler, Pflanzenr. 4(48): 49. 1902. For a full 
nomenclatural account see Suksathan & Borchsenius 
(2005). 

Fig. 2. . Phrynium robinsonii  (Valeton) Suksathan & Borchs. 



2010]                      219   ARDIYANI et al.: Marantaceae in Sulawesi 

Rhizomatous ground herb, 1.7–4 m tall. Leaf 
blade 40–85x20–45 cm, glabrous. Inflorescence 
produced directly from the rhizome, erect, simple, 
cylindric or somewhat laterally compressed; 
peduncle 6–33 cm long, spike 11–25 cm long; 
fertile bracts 9–18, distichous; flower pairs (1–) 3–4 
per special paraclade. Flowers white to creamy 
white, slightly fragrant; 3.5–5 cm long, sepals to 4 
mm long; corolla tube 24–40 mm long. Fruits 
broadly ellipsoid, pale brown, ca. 14x12 mm; seeds 
1–2, with a large bifid aril. 
 
 
Distribution. Widespread in the west Malesian 
region, from southern Thailand and Peninsular 
Malaysia to Java, Sumatra, Borneo and Sulawesi 
(first record). 
 
Habitat and ecology. Small forested hill in garden 
area. 
 
Notes. The species is readily recognized by its 
spicate inflorescences, with distichous fertile bracts, 
that arise on separate shoots from the leaf-bearing 
ones. Detailed botanical descriptions based on 
material from Borneo and Thailand, respectively, 
are provided by Clausager & Borchsenius (2003) 
and Suksathan & Borchsenius (2008). The single 
recent collection (Poulsen et al. 2805) represents an 
extension of the known range of the species across 
Wallace's line. This species is sometimes cultivated 
in Malaysia and it is difficult to rule out entirely that 
it has escaped from cultivation. The plants were, 
however, collected in a more or less primary forest 
patch amongst cocoa plantations etc. far from the 
nearest village. The locals also thought it was 
native. Lacking collections of this species from 
several primary forest sites nor evidence of 
cultivation, we cannot be certain whether it has 
been introduced. 
 
 
Specimens seen from Sulawesi. Central Sulawesi. 
Samawati (1°1'31.2''N, 121°36'16.2''E), 40 m, 21 
February 2009, flowering, Poulsen & Kinho 2805 (AAU, 
BO). 
 
 
6. STACHYPHRYNIUM REPENS (Körn.) 
Suksathan & Borchs. 
 

Stachyphrynium repens (Körn.) Suksathan & Borchs. 
, Taxon 54 (4): 1086 (2005). — Phrynium repens Körn., 
Bull. Soc. Imp. Naturalistes Moscou 35(1): 103 (1862). – 
Type: Java, Göreng 408 (Turczaninow herb., KW?, 
LE?). 

Stachyphrynium jagorianum (K. Koch) K. Schum. in 

Engler, Pflanzenr. 4(48): 48. 1902. For a full 
nomenclatural account see Suksathan & Borchsenius 
(2005) 
 

Rosulate herb, to 55 cm tall, frequently forming 
large colonies on the forest floor. Leaves 1–3 per 
shoot; lamina elliptic to oblong, acute to acuminate, 
10–20x3.5–5.5 cm, green to dark green above, with 
more-or-less pronounced darker green stripes 
following the major veins, pale below, glabrous or 
pubescent. Inflorescence interfoliar, erect, usually 
simple; peduncle 5–14 cm long; spike 2.5–7.5 cm 
long with 3–6 distichous fertile bracts; flower-pairs 
2 per special paraclade but usually only 1 pair 
develops. Flowers white, ca. 10 mm long; sepals to 
2.5 mm long; corolla tube 13–18 mm long. Fruits 
broadly ellipsoid to obovate, to 4x5 mm; seeds 1–2, 
with a large bifid aril. 
 
Distribution. Indo-China, Thailand, Peninsular 
Malaysia and Indonesia: Sumatra, Java and 
Sulawesi (first record). Not recorded in Borneo. 
 
Habitat and ecology. Forest-savanna mosaic on 
sandy soil. 
 
Notes. Easily recognised by its small size and the 
dark green oblique bands on the upper side of  the 
leaves. A detailed botanical description of this 
species is provided by Suksathan & Borchsenius 
(2008). This record represents an extension of the 
known range of the species across Wallace's line. 
Only one collection is known from Sulawesi 
(Poulsen et al. 2797) but we found S. repens at 
several localities south of Kendari and it appears to 
have dispersed to SE Sulawesi a long time ago. 
 
Specimens seen from Sulawesi. Southeast Sulawesi. 
Tatangge Forest Reserve, Tatangge (4°27'35.6''S, 122°
7'28.1''E), 20 m, 13 February 2009, flowering and 
fruiting, Poulsen, Ardiyani, Chahyadi, Gufrin & Lasifu 
2797 (AAU, BO, E). 
 

 
ACKNOWLEDGEMENTS 
 

Fieldwork by Axel Dalberg Poulsen in Sulawesi was 
sponsored in 2008 by the Carlsberg Foundation (grant 
number 2007_01_0568) and in 2009 by the Augustinus 
Foundation, the Peter Davis Expedition Fund, and the 
Blaxall Valentine Awards of the Royal Horticultural 
Society, UK. Further work was supported financially by 
the Carlsberg Foundation (grant number 2007_01_0626 
to Finn Borchsenius). We thank the State Ministry of 
Research and Technology (RISTEK) for permits to do 
research in Indonesia and local botanists and institutions 
in Sulawesi for help with logistics, especially Theogives 
Lasut, Ramadhanil Pitopang, Firdaus and Julianus Kinho. 



  REINWARDTIA  220                                [VOL.13 

 

 

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KOORDERS, S. H. 1898. Verslag eener botanische 
dienstreis door de Minahasa tevens eerste overzicht 
der flora van N.O. Celebes uit een wetenschappelijk 
en praktisch oogpunt. Mededeelingen van's Lands 
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POULSEN, A. D. & CLAUSAGER H. 2004. A new 
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SCHUMANN, K.M. 1902. Marantaceae. In: Engler, A. 

(ed.), Das Pflanzenreich IV. 48 (Heft 11). Verlag von 
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SUKSATHAN, P. & BORCHSENIUS, F. 2003. Two 
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SUKSATHAN, P. & BORCHSENIUS, F. 2005. 
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Thailand. Taxon 54: 1083–1090.  

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A. D. 2006. Schumannianthus monophyllus (Maran-
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BORCHSENIUS, F. 2009. Phylogeny and generic 
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REINWARDTIA  
Vol. 13. No. 2. 2010  

CONTENTS  
Page 

 
HARRY WIRIADINATA & RISMITA SARI. A new species of Rafflesia (Rafflesiaceae)  
from North Sumatra ………………………………………………………………………..……………….. 95 
 
ARY  P. KEIM. A new species of Freycinetia (Pandanaceae) from Papua New Guinea………………… 101 
 
ROBERT GRADSTEIN et al. Bryophytes of Mount Patuha, West Java, Indonesia……………………...  107 
                                                                                                                                                              
ABDULROKHMAN KARTONEGORO & J. F. VELDKAMP. Revision of Dissochaeta  
(Melastomataceae) in Java, Indonesia………………………………………………………...…………… 125 
  
NURSAHARA PASARIBU. Two new species of Freycinetia (Pandanaceae) from Sumatra,  
Indonesia………………………………………………………………………………………………….... 147 
 
ARY P. KEIM. & M. RAHAYU.  Pandanaceae of Sumbawa, West Nusa Tenggara, Indonesia................ 151 
 
K. MAT-SALEH, RIDHA MAHYUNI, AGUS SUSATYA, J. F. VELDKAMP. Rafflesia  
lawangensis (Rafflesiaceae), a new species from Bukit Lawang, Gunung Leuser National Park,  
North Sumatra, Indonesia.............................................................................................................................. 159 
 
J. F. VELDKAMP & R. M. K. SAUNDERS. Goniothalamus tripetalus (Lam.) Veldk.  
& R. M. K. Saunders (Annonaceae), comb. nov. .......................................................................................... 167 
 
M. M. J. VAN BALGOOY. An updated survey of Malesian Seed Plants Families..................................... 171 
 
NURHAIDAH IRIANY SINAGA. Two new species of Freycinetia (Pandanaceae) from 
Manokwari, West Papua ............................................................................................................................... 183 
 
NURHAIDAH IRIANY SINAGA, RITA MEGIA, ALEX HARTANA & ARY PRIHARDHYANTO 
KEIM. The ecology and distribution of Freycinetia Gaud. (Pandanaceae; Freycinetoideae) in the  
Indonesian New Guinea................................................................................................................................  189 
 
EIZI SUZUKI. Tree flora on freshwater wet habitats in lowland of Borneo: Does wetness cool the sites.. 199 
 
NANDA UTAMI & HARRY WIRIADINATA. Impatiens mamasensis (Balsaminaceae), a new  
Species from West Celebes, Indonesia.......................................................................................................... 211 
 
M. ARDIYANI, A. D. POULSEN, P. SUKSATHAN, F. BORCHSENIUS. Marantaceae in Sulawesi..... 213 
 
 
 
 
 
 
 
 
Reinwardtia is a LIPI acredited Journal (258/AU 1/P2MBI/05/2010)  
 
Herbarium Bogoriense  
Botany Division  
Research Centre for Biology – LIPI  
Cibinong, Indonesia  


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