Research Article |
Corresponding author: Michal Hroneš ( michal.hrones@upol.cz ) Academic editor: Vincent Droissart
© 2025 Michal Hroneš, Michal Sochor, Alena Uvírová, Azlan bin Pandai, Salwana Jaafar, Rahayu S. Sukri, Martin Dančák.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Hroneš M, Sochor M, Uvírová A, bin Pandai A, Jaafar S, Sukri RS, Dančák M (2025) Gastrodia microchila (Orchidaceae, Epidendroideae), a new species from Brunei Darussalam. PhytoKeys 256: 1-11. https://doi.org/10.3897/phytokeys.256.149020
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A new orchid species, Gastrodia microchila is described and illustrated. The species was found in a mixed dipterocarp forest in the Belait district, Brunei Darussalam, northern Borneo in 2024. It is distinct from most Gastrodia species in western Malesia by its small lip and column, and presence of the smooth cushion-like tissue on the inner side of lateral sepals. Gastrodia microchila is only the second species of Gastrodia recorded for Brunei Darussalam and the seventh known species for Borneo. A determination key for all Gastrodia species occurring in western Malesia is also provided.
Borneo, endemic species, holomycotrophic orchid, Malesia, mycoheterotrophy, tribe Gastrodieae
The mycoheterotrophic flora of north-western Borneo (Sarawak and Brunei Darussalam) is exceptionally rich, including more than twenty species of Thismia (Thismiaceae), five species of Epirixanthes (Polygalaceae) and eleven species of Sciaphila (Triuridaceae) (
The genus, if treated in the wide sense, comprises 107 species (
Species of Gastrodia are achlorophyllous, mycoheterotrophic herbs with reduced vegetative organs and fleshy tuberous rhizomes (
In total, the occurrence of sixteen species is reported from western Malesia. Of these, only Gastrodia javanica (Blume) Lindl. is widespread, G. bambu Metusala occurs in Java and Vietnam, G. effusa P.T. Ong & P. O’Byrne in Borneo and Malay Peninsula, G. exilis Hook.f. in southern India, Assam, Thailand, Cambodia and Sumatra, G. spathulata (Carr) J.J. Wood in Borneo and Java and G. verrucosa Blume in Java, Sumatra and Thailand (
During our ongoing research on mycoheterotrophic plants of Brunei Darussalam, we found a second species of Gastrodia for the country which did not resemble any species reported from Borneo. After a thorough examination of its morphology, it is described here as a new species.
This study is based on the material collected in November 2024 in a forest on the northern slopes of Telingan Hill (Belait district), Brunei Darussalam. Morphological characters were studied on living plants and documented by macro photography. Morphological characters were compared with the protologues and relevant floristic literature of Gastrodia species from western Malesia, i.e. Borneo, Java, Peninsular Malaysia and Sumatra (
Brunei Darussalam • Belait district: Labi village, northern slopes of Bukit Telingan, mixed dipterocarp forest ca. 1.8 km E of primary school in Kampung Rampayoh, 4.37672°N, 114.47339°E, 200 m alt., 25 Nov 2024, Hroneš 2024/4 (holotype: BRUN B 045 889).
Gastrodia microchila is similar to G. holttumii Carr from Peninsular Malaysia but differs by narrower cylindrical rhizome without distinct nodes (vs. robust, distinctly noded), flowers 8.5–9.0 mm wide, narrowly open (vs. 9.0–11.0 mm wide, widely open), free part of lateral and dorsal sepals oblong triangular to broadly triangular, up to 4.5 × 5.0 mm (vs. elliptic to oblong elliptic, 6.0–7.0 × 3.0–5.0 mm), free part of petals indistinct, ca. 0.7 × 0.6 mm, elliptic (vs. 1.0–2.0 × 0.7–1.0 mm, ovate), hypochile 2.0 × 2.0 mm, broadly oblong-orbicular (vs. 2.0 × 1.5 mm, oblong-ovate) and stelidia longer than anther cap (vs. subequal to anther cap).
Gastrodia microchila Hroneš A habit of flowering plant B fruiting plant with capsules on elongated pedicels C detail of inflorescence with side view of flower D front view of flower E inflorescence viewed from above F flower viewed from below with connate and free part of lateral sepals, and ovary G dissected synsepalum showing minute petals and cushion-like smooth tissue on the internal side of sepals H part of the stem with leaf I tuber A–I from Hroneš 2024/4 (Photo M. Hroneš).
Terrestrial, achlorophyllous herb, 16–21 cm tall. Rhizome ca. 50 mm long, 3–6 mm in diameter, tuberous, fleshy, cylindrical, without distinct nodes, densely covered by filiform scales. Stem 128.5–165.0 mm long, 1.8–2.2 mm in diameter, with 4–6 nodes, ± erect, indistinctly ridged, covered by low blunt verrucae, whitish brown, pale greyish brown to beige. Leaves 2.7–5.5 mm long, 2.5–3 mm wide at base, scale-like, broadly triangular, basally clasping, tip acute to erose, brown. Bracts subtenting base of each pedicel 2, unequal in size; longer one 4.0–4.5 mm long and 2.8–3.4 mm wide, broadly triangular, clasping basally, keeled, persistent, covered by low blunt verrucae, brown; shorter one 3.7–4.6 mm long, ca. 0.5 mm wide at base, 1.5–1.8 mm wide in the middle part, stipitate ovate to stipitate triangular with tapering tip, keeled, caducous in lower flowers. Inflorescence loose, 2–4 flowered; rhachis 8.5–10.5 mm long. Pedicel 2.5–5.3 mm long, 1.0–1.4 mm in diameter, elongating to 12.5–100.0 mm in fruit, with 6 distinct ribs, becoming smoother in fruit, greyish pink to pinkish orange. Flower (excluding ovary) 13.0–15.0 mm long, 8.5–9.0 mm wide, spreading almost horizontally, narrowly open, with sepals and petals basally fused, forming a five-lobed, tubular campanulate perianth tube; flower bud pinkish orange. Sepals externally pale pinkish orange, covered by low blunt verrucae (more distinct in young flowers), internally pinkish orange at base and whitish orange to beige apically. Lateral and dorsal sepals connate into synsepalum for ca. 2/3 of their length, lateral sepals connate for up to 1/2 of their length, connation perfect for basal 3–4 mm, additional 3–5 mm connate imperfectly, leaving a conspicuous furrow on the surface of flower; free portion 4.0–4.5 × 4.5–5.0 mm, oblong triangular, cucullate, blunt at apex, with irregular translucent margin, internally with beige-orange to deep orange-pink, cushion-like smooth tissue covering most of the sepal space. Free portion of dorsal sepal 5.0 × 5.0 mm, broadly triangular, blunt and shortly cucullate at apex, with irregular translucent margin. Free portion of petals indistinct, ca. 0.7 × 0.6 mm, elliptic, whitish orange to beige, almost translucent. Lip ca. 3.0 × 2.0 mm, adnate to base of column, greyish pink to beige; hypochile ca. 2.0 × 2.0 mm, thick and fleshy, almost flat, broadly oblong-orbicular; epichile 1.0 × 0.8 mm, oblong to almost rectangular with wide obtuse apex bent downwards, orange to reddish brown; keel ca. 0.4 mm wide, positioned at the transition of hypochile and epichile, hypochile part beige, epichile part reddish brown, with margins raised into two low ridges which have the tallest part at the transition between hypochile and epichile; calli ca. 0.2 × 0.2 mm, ± globose, pale orange-brown. Column ca. 3.0 × 1.9 mm, straight, oblong to rectangular, canaliculate, winged, without distinct rostellum, central part beige, wings slightly ventricose, beige, basally pale pinkish orange; stelidia ca. 0.8 mm long, terete, elliptic-triangular, obtuse, beige, slightly exceeding anther; anther cap ca. 0.6 × 0.9 mm, rectangular-ovate; pollinia not seen; stigma not seen. Ovary 2.3–5.0 × 1.8–2.6 mm, attached at an angle to pedicel, obconical, bluntly trilobed in intersection, slightly ventricose, with 3 high and 3 low ribs alternating to each other, covered by low blunt verrucae, greyish pink basally, greyish brown apically. Capsule 13.2–15.6 × 4.0–5.1 mm, cylindrical-fusiform, greyish pink in most part, brown apically.
Endemic to Brunei Darussalam. So far known only from its type locality in the Belait District. It grows in mixed dipterocarp forest on shady and humid slopes near the small streams. The forest was probably lightly logged in the past.
Gastrodia microchila Hroneš A habit of flowering plant B detail of inflorescence with bracts C dissected synsepalum with free parts of sepals and petals D flower viewed from above E flower viewed from below F front view of flower G lip H column A–H from Hroneš 2024/4 (Illustration V. Blažek).
The name is derived from the Latin micro- = small and -chilum = lip, referring to the size of the lip, which is among the smallest in Gastrodia species in western Malesia.
The species is currently known from a single small population spanning less than 500 m2. Fewer than ten individuals were observed at the site. The population is located in currently unprotected forest. Consequently, any random natural or human-induced event could destroy the site and the entire population. Therefore, we propose to preliminarily treat G. microchila as critically endangered (CR) based on the B2ab(iv)+D criteria.
The discovery of G. microchila represents the second known species of the genus in Brunei Darussalam (
The most (and only) similar species to G. microchila in western Malesia is G. holttumii from Peninsular Malaysia (
Due to its tubular-campanulate flowers covered by low blunt verrucae, G. microchila is also superficially similar to several Gastrodia species from western Malesia, especially G. abscondita J.J.Sm., G. bambu, G. crispa J.J.Sm., G. maliauensis, G. selabintanensis Tsukaya & A.Hidayat, and G. verrucosa. However, it differs from them by its very small lip and column which both are only ca. 3.0 mm long (vs. 4.0–12.0 mm long lip and 5.5–12.0 mm long column in the rest of the species). Gastrodia microchila also has very short petals when compared to other species. Its petals are less than 1 mm long, almost indistinct in some flowers. Another distinct morphological trait of G. microchila is the smooth cushion-like tissue located on the inner side of lateral sepals. To the best of our knowledge, this tissue is absent in the above-mentioned species, but we cannot rule out the possibility that it was overlooked, especially in species described from dry specimens (
1 | Perianth split between the lateral sepals almost to the base with lip visible between the lateral sepals, calli on the lip absent | G. javanica |
– | Perianth tube completely connate basally for at least 1/3 of its length and enclosing the lip, calli on the lip present | 2 |
2 | Free part of petals inserted deep in synsepalum | 3 |
– | Free part of petals terminal | 4 |
3 | Petals connate to synsepalum for 1.5 mm, apical part claviform, fimbriate | G. spathulata |
– | Petals connate to synsepalum for 9.5 mm, apical part spatulate, glabrous | G. dewildeorum |
4 | Free part of petals almost of the same size and shape as sepals, lip and column protruding from the flower | G. effusa |
– | Free part of petals distinctly smaller and of different shape as sepals, lip and column hidden inside the flower | 5 |
5 | Petals fimbriate, sepals smooth, fragile | G. exilis |
– | Petals entire to irregularly dentate, sepals externally with low blunt verrucae, fleshy | 6 |
6 | Lateral sepals with verrucose cushion-like tissue on its inner surface | 7 |
– | Lateral sepals with smooth cushion-like tissue or flat on its inner surface | 9 |
7 | Flowers (excl. ovary) ca. 11.8 mm long, ca. 9.0 mm in diam., lip ca. 5.0 mm long, hypochile 4.0 mm wide | G. callosa |
– | Flowers (excl. ovary) 12.0–16.0 mm long, 13.0–28.0 mm in diam., lip 7.0–9.0 mm long, hypochile 4.5–6 mm wide | 8 |
8 | Flowers very widely campanulate, up to 28.0 mm wide, hypochile almost orbicular, column wings with claw-like thick process | G. tembatensis |
– | Flowers campanulate, up to 12.5 mm wide, hypochile broadly elliptic, column wings with triangular process | G. sabahensis |
9 | Lip and column ca. 3.0 mm long, lateral sepals internally with cushion-like smooth tissue | 10 |
– | Lip and column at least 4.0 mm long, lateral sepals without cushion-like tissue internally | 11 |
10 | Flowers 8.5–9.0 mm wide, narrowly open, free part of sepals up to 4.5 × 5.0 mm, oblong triangular to broadly triangular, free part of petals small, ca. 0.7 × 0.6 mm, stelidia longer than anther cap | G. microchila |
– | Flowers 9.0–11.0 mm wide, widely open, free part of sepals 6.0–7.0 × 3.0–5.0 mm, elliptic to oblong elliptic, free part of petals distinct, 1.0–2.0 × 0.7–1.0 mm, stelidia subequal to anther cap | G. holttumii |
11 | Flowers relatively small, up to 10.0 mm long, free part of sepals up to 3.5 mm long, lip 4.0 mm long with hypochile ca. 2.7 mm wide | G. verrucosa |
– | Flowers larger, more than 10.0 mm long, free part of sepals at least 4.0 mm long, lip at least 6.0 mm long with hypochile at least 3.5 mm wide | 12 |
12 | Lip white, yellowish white to brownish white | 13 |
– | Lip brown, purplish brown to green | 15 |
13 | Flowers subglobose to widely campanulate, free part of sepals distinctly wider than long, lip broadly oblong to quadrate | G. grandilabris |
– | Flowers tubular to tubular campanulate, free part of sepals of ca. same length and width, lip ovate to elliptic | 14 |
14 | Lip 7–8 mm long, shorter to about the same length as column | G. crispa |
– | Lip 10–12 mm long, longer than column | G. selabintanensis |
15 | Flowers 17.0–20.0 × 14.0–16.0 mm in diam., lip 10.0–12.0 × 3.5–4.0 mm, oblong-lanceolate | G. bambu |
– | Flowers up to 13.0 × 11.0 mm in diam., lip up to 7.0 × 4.0 mm, ovate-triangular to ovate | 16 |
16 | Petals 3.7 × 1.7 mm, oblong, lip green with orange apex | G. abscondita |
– | Petals 1.8 × 2.2 mm, ovate to (sub)orbicular, lip dark brown with almost black apex | G. maliauensis |
We would like to thank field assistants from the Institute for Biodiversity and Environmental Research (IBER) and Brunei National Herbarium (BRUN), in particular Mohamad Farid bin Abdullah and Watu bin Awok for their help in the field, and to Vojtěch Blažek, who kindly prepared an illustration of the species. We also thank the UBD Botanical Research Centre, in particular Nur Ammy Marliana Liming, for assistance with herbarium specimens. André Schuiteman and Ong Poh Teck kindly provided literature.
The authors have declared that no competing interests exist.
No ethical statement was reported.
This research was supported by Internal Grant Agency of Palacký University IGA_PrF_2025_001, IGA_PrF_2025_017 and by institutional support MZE-RO0423 from the Ministry of Agriculture of the Czech Republic. We thank Universiti Brunei Darussalam and the Brunei Forestry Department for permission to conduct research in Brunei’s forests (Permit ref.: JPH/UND/17[JPH/IND/SPL/FORM7/2024/041]).
MH: conceptualization, field work, species description, original draft writing; MS: field work, draft improvement and editing; AU: field work, draft improvement and editing; AP: field work, draft improvement and editing; SJ: field work, draft improvement and editing; RS: project oversight, resource provider, draft improvement and editing; MD: project oversight, field work, draft improvement and editing.
Michal Hroneš https://orcid.org/0000-0002-0380-929X
Michal Sochor https://orcid.org/0000-0002-6525-1295
Alena Uvírová https://orcid.org/0009-0000-8608-2032
Salwana Jaafar https://orcid.org/0000-0003-0224-9603
Rahayu S. Sukri https://orcid.org/0000-0002-2662-399X
Martin Dančák https://orcid.org/0000-0002-3851-4969
All of the data that support the findings of this study are available in the main text.