Research Article
Print
Research Article
Castanopsis corallocarpus (Fagaceae), a new species from Royal Belum (Perak) in Peninsular Malaysia
expand article infoWei Harn Tan§|, Lisa Ong §, Joeri Sergej Strijk|#
‡ Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences & Center for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Yunnan, China
§ The University of Nottingham Malaysia, Semenyih, Malaysia
| Universiti Brunei Darussalam, Bandar Seri Begawan, Brunei
¶ Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences & Center for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Mengla, Yunnan, China
# Alliance for Conservation Tree Genomics, Pha Tad Ke Botanical Garden, Luang Prabang, Laos
Open Access

Abstract

A new species from the Fagaceae family, Castanopsis corallocarpus Tan & Strijk, is described from Royal Belum State Park in Peninsular Malaysia. Here, we provide technical illustrations, colour images and a description of its conservation status and the collecting locality, in addition to a comparative analysis with other species in the region. The solitary nut of C. corallocarpus has a morphologically unique cupule, lined with rows of thick coral-like spines not seen in other Castanopsis species.

Keywords

Berangan, chinquapins, flora of Peninsular Malaysia, hill dipterocarp forest, Malayan chestnut

Introduction

Castanopsis (D.Don) Spach, is the third largest genus in Fagaceae, comprising ca. 134 species (Phengklai 2008; Li et al. 2015; Strijk 2022). Apart from limestone formations, Castanopsis species can be found in various habitats, ranging from lowland rainforest to montane forest and even harsh environments, like acidic heaths and peat swamps (Soepadmo 1972). Many seem to have narrow ecological or habitat preferences though, with species often found on ridges or crests and along margins and riverbanks. All Castanopsis species are medium to large trees and, like other Fagaceae species, are co-dominant in the closed canopy layer (Soepadmo 1972). The wide geographical distribution of Castanopsis is restricted to (sub-)tropical Asia, ranging from north-eastern India (Nepal, Bhutan and Assam), parts of eastern Asia (southern China, Korea and Japan) and southeast Asia (Indochina and Malesia). The genus has two major biodiversity hotspots, namely Indochina and Malesia (Soepadmo 1972). New taxonomic discoveries of Castanopsis are skewed towards Indochina with eight new species having been described in the last few decades (Phengklai 2004; Chen et al. 2010; Chen et al. 2011; Vuong and Xie 2014; Hoang et al. 2018; Mitra et al. 2019). Interestingly, no new species of Castanopsis has been described in Malesia over the last two decades.

The dipterocarp-dominated tropical rainforests of Peninsular Malaysia are part of the megadiverse Sundaland forest range (Myers et al. 2000). It is estimated that Peninsular Malaysia has at least 9,030 vascular plant taxa comprising 248 families and 1,651 genera (Yong et al. 2021). The Fagaceae family is an important component of the rainforest in Peninsular Malaysia, with a total of 72 species comprising four genera (i.e. Castanopsis, Lithocarpus, Quercus and Trigonobalanus). Mast fruiting phenomena in the Sundaland occur on an irregular suprannual scale (2–10 years) for many plant families, resulting in long periods of crop scarcity (Medway 1972). Unlike most mast-fruiting families, tropical Fagaceae communities fruit annually at unsynchronised times throughout the year, providing an important food source for many animals during periods of low fruit availability (Kaul et al. 1986). Species in the genus are known as ‘Chinquapin’ (not to be confused with two species in the North American genus of Chrysolepis (Fagaceae), which are also often referred to as such). Locally, the genus is known as berangan in Malay or the Malayan chestnut (Corner 1988). There are 20 described Castanopsis species in Peninsular Malaysia and, of these, five species are endemic to Malaysia (Cockburn 1972; Soepadmo 1972; Strijk 2022).

Royal Belum State Park is in the State of Perak, in the north of Peninsular Malaysia. The rainforest of Belum consists of undisturbed and pristine lowland dipterocarp, hill dipterocarp and lower montane forests. Belum is part of the larger Belum-Temenggor Forest Complex (BTFC) which has an area of ca. 3,500 km2. The BTFC is also part of a larger forest complex, as it shares a border with two adjacent protected areas in Thailand (Hala-Bala Wildlife Sanctuary and Bang La National Park) and forms part of the Central Forest Spine of Peninsular Malaysia. A product of the geological merger between the supercontinents of southern Gondwanaland and northern Laurasia, the landscape of BTFC is estimated to be more than 130 million years old, which is older than the Amazon and Congo Basins (Malaysian Nature Society 2005). Given its unique position within the Peninsula, the rich floristic composition of BTFC is a mixture of Thai-Burmese and Malayan flora with approximately 3000 species of flowering plants recorded, many of which are endemic to northern Peninsular Malaysia (Malaysian Nature Society 2005).

During a field expedition in Royal Belum State Park, Malaysia in July 2018, we came across a specimen with a large single nut and a unique burr that does not match any described taxa of Castanopsis. After examining the relevant literature on Malesian Fagaceae, we report this specimen as a new species, placed within the genus Castanopsis.

Taxonomy

Castanopsis corallocarpus W.H.Tan & Strijk, sp. nov.

Figs 1, 2

Type material

Holotype. Malaysia, Sungai Tiang, Royal Belum State Park, Hulu Perak District, Perak State, elevation 417 m, 11 January 2022, W.H. Tan TWH002, Holotype: KEP; Isotypes: IBER [IBER00000000030; IBER00000000031]. Paratype. Malaysia, Sungai Papan, Royal Belum State Park, Hulu Perak District, Perak State, elevation 290 m, W.H. Tan TWH003, Paratype: KEP; IBER [IBER00000000032, IBER00000000033]. Due to the small number of individuals and precarious conservation status, detailed locality information is not released here, but can be requested from the authors.

Figure 1. 

Castanopsis corallocarpus W.H.Tan & Strijk, sp. nov. W.H.Tan TWH002 (KEP) A fresh fruit from field collection B leaves and twigs from field collection C bark and sapwood D fresh nut – top view, side view, front view E young emerging leaf F mature fruit with splitting valves on the cupule – front view, top view G petiole H fresh mature – side view, front view, top view I young infructescence spike. All pictures by W.H.Tan and J.S.Strijk.

Diagnosis

Castanopsis corallocarpus is a medium-sized tree. It differs from similar species by its fruits which carry unique rows of basally reinforced, blunt coral-like spines on the cupule exterior, combined with singular rounded rectangular nuts which are slightly asymmetric. Currently, the species has been found in two localities, both in Royal Belum State Park and each consisting of one individual. Several additional individuals resembling C. corallocarpus were reported by our field staff in Temenggor Forest Reserve, Perak, but this is awaiting confirmation. Pending further discoveries, the species appears to be locally restricted to low-mid elevation forests of the BTFC.

Figure 2. 

Castanopsis corallocarpus W.H.Tan & Strijk, sp. nov. W.H.Tan TWH002 (KEP) A habit B young infructescence spike C close-up of coral-like spine D mature nuts-bottom, top view and fruits-bottom, top and side view. Illustration by L. Ong.

Description

Medium size tree, approximately 16–20 m tall, no buttresses. Bark lenticellate grey. Sapwood reddish-brown to pink. Branches glabrous, densely lenticellate, dark-brown to grey-white. Leaves simple, thin-coriaceous, papery when dried, lamina elliptic, up to (11)13–17(19) × (2)3.5–5(6) cm. Leaf apex acuminate; base cuneate, occasionally somewhat asymmetric. Margin entire. Both surfaces glabrous. Leaves dark green above and glaucous below. New shoots exhibit flushing. Venation pinnately veined, secondary venation eucamptodromous. Pairs of secondary veins 9–10(11), raised on underside of leaf. Tertiary veins scalariform, but scarcely visible on underside. Male and female inflorescences not seen. Peduncles 7–11 cm long, up to 0.4 cm in diam. at the base, glabrescent, grey-brown and densely lenticellate. Infructescence a woody spike, terminal, ranging from 9–10 cm. Fruits sessile on woody peduncle, spread out on spike and not clumped. Very few fruits make it to maturity, with typically 1–3 units fully ripening. Acorn globose or ovoid when developing, globose when mature, 3.3–3.8 × 2.7–3.3 cm, covered with 4–5 eccentric ridges with blunt thick coral-like spines, originating from the style scar looping towards the suture that runs along the spine of the fruit, surface puberulous. Cupule fully enclosing the nut, mostly indehiscent, but occasionally dehiscent, exposing exocarp area. Fresh cupule wall bright green, suture dark grey-black. Old cupule grey-green, darker on the surface lighter on the spines. Nut 1 in each cupule, oblong in shape, flat at the bottom, 2.5–2.9 × 2.3–2.4 cm, tip pointing down. Up to 90% of the surface area of the nut comprising scar area (receptacle tissue) and up to 10% of the surface area of the nut is slightly raised and made up of vestigial exocarp layer. Nut scar pale brown-whitish with glabrous, rugose surface, adnate to the cupule, exocarp layer light brown, covered in thin layer of silvery tomentum.

Phenology

Flowering and fruiting occur annually, with flowers appearing in March and fruits maturing in July to August. Sporadic fruiting was observed in November and December 2021.

Distribution, habitat and ecology

Castanopsis corallocarpus is only known from the Belum-Temenggor Forest Complex, Hulu Perak District, Perak, Malaysia. Within BTFC, this species has been officially recorded in Sungai Tiang and Sungai Papan as shown in Fig. 3. This species grows in both lowland and hillside dipterocarp forests (300–450 m above sea level) with a soil type of low nutrient and high clay abundance typical of most dipterocarp forest. As Peninsular Malaysia is situated near the Equator, the climate is classified as wet equatorial, characterised by high daytime temperature and high rainfall throughout the year. According to The Malaysian Meteorological Department (2022), the District of Hulu Perak experiences an average rainfall of 1500–2000 mm annually and the daytime temperature is around 27–30 °C and 21–24 °C at night with very minimal fluctuations seasonally.

Figure 3. 

Collections sites of Castanopsis corallocarpus W.H.Tan & Strijk in Belum-Temenggor Forest Complex.

Vernacular name

Both indigenous communities of BTFC (i.e. the Jahai and Temiar) do not have a specific name in their language, instead referring to it in Malay as Berangan.

Etymology

The epithet corallocarpus, a noun in apposition, alludes to thick coral-like spikes arranged in undulating thickened ridges on cupule of fruit.

Conservation status

Based on the guidelines established by the IUCN Red List (IUCN 2022), we provide an initial assessment of the species here as Critically Endangered (CR B1B2ab(i,ii,iii,iv)), based on only two recorded individuals within Royal Belum State Park, small known range (BTFC) and the extensive habitat alteration and forest clearance throughout the immediately adjacent wider region. Although Royal Belum State Park is fully protected from logging, the southern part of BTFC namely Temenggor Forest Reserve is open to exploitation, further threatening to shrink its already small range.

Discussion

We report the first description of a new species, C. corallocarpus from BTFC, Perak, Malaysia. Peninsular Malaysia has a total of 20 species of Castanopsis and C. corallocarpus is easily distinguished by the unique rows of basally reinforced, blunt coral-like spines on the cupule. At least 10 species of Castanopsis species have a single nut and out of these, only two have a non-spiny cupule (i.e. Castanopsis curtisii King and Castanopsis nephelioides King ex Hook.f.). All others have either short-dense spines (Castanopsis megacarpa Gamble; Castanopsis malaccensis Gamble; Castanopsis johorensis Soepadmo; Castanopsis javanica (Blume) A.DC.; Castanopsis tungurrut (Blume) A.DC.; Castanopsis ridleyi Gamble) or thick thorns (Castanopsis rhamnifolia (Miq.) A.DC. and Castanopsis acuminatissima (Blume) A.DC.) as their main defence against seed predation.

Peninsular Malaysia and Borneo together have an estimated 103 species of Fagaceae in four genera (Castanopsis: 22; Lithocarpus: 62; Quercus: 18; Trigonobalanus: 1; Royal Botanic Gardens Kew (2021)). Numbers for the individual Bornean regions (Sabah, Sarawak, Brunei and Indonesian Kalimantan) fluctuate, depending on source and species-data considered, but it is estimated that, for the two major areas (PM and Borneo s.l.), endemism in Peninsular Malaysia is highest for Castanopsis only, whereas on Borneo, all three main genera have significant levels of endemicity (Peninsular Malaysia: C: 22%; L: 1%; Q: 0 (no endemics); Borneo s.l.: C: 46%; L: 91%; Q: 100% (all species endemic)). Many species in Lithocarpus and Quercus have ranges restricted to mid- or higher elevation habitat (> 600 m), which is more prevalent in Borneo (Soepadmo 1972), while occurrence and diversity of Castanopsis species seem to be less extremely governed by elevation, but more by the prevalence of ridges, crests, forest- and river-margins (Cockburn 1972; Soepadmo 1972).

Of the five Castanopsis species endemic to Peninsular Malaysia, four are found mostly in mid- to upland habitats, all first described from Perak (Larut and surrounding areas). A fifth endemic (C. selangorensis A.Camus) was primarily found in the lowlands, but is presumed extinct (Cockburn 1972). Castanopsis corallocarpus, a sixth endemic species of Castanopsis for Peninsular Malaysia, differs distinctly in its distribution by occurring only in the north in the lowland and hillside forest (< 450 m). Within Malaysia and the wider region, C. corallocarpus is unique in its combination of properties and we further outline some of the defining differences with other species in Table 1.

Table 1.

Morphological differences between C. corallocarpus and other species of Castanopsis of the Peninsular region.

Characters C. corallocarpus W.H.Tan & Strijk C. inermis (Lindl.) Benth. & Hook.f. C. purpurea Barnett C. pierrei Hance C. rhamnifolia Miq. A.DC.
1. Cupule surface Cupule with basally reinforced, blunt coral-like spines arranged in continuous ridges. Ridges in young fruits often terminate only a few mm apart, resulting in hollow enclosures protecting the exterior inner cupule. Cupule sparsely covered with simple, short, curled thorns set in 3–5 lines. Cupule sparsely covered with woody, branched, curved spines. Cupule sparsely covered with woody, branched, curved spines. Cupule covered with tufted, erect, simple thorn-like structures.
2. Number of cupule valves 3(–4) 2(–4) “dehiscent”, #valves unreported “dehiscent”, #valves unreported 3– (4?), or indehiscent
3. Number, size of acorns (l × w) 1, 3.3–3.8 cm × 2.7–3.3 cm. (1)2–3, 1.5–2.5 cm × 1.5–3.5 cm. 1–3 (4), 4.5–6 cm in diam. 1–3 (4), 4–6 cm in diam. 1, 1–1.5 cm × 1–1.5 cm.
4. Acorn shape (ripe), position Acorn globose, sessile and solitary. Irregularly globose, sessile and clustered (sometimes fused). Globose, stalked and solitary. Irregularly globose or bilobed, semi-stalked to sessile and solitary. Asymmetrically depressed subglobose, sessile solitary or in pairs.
5. Acorn surface Pustulated Pustulated Unreported Pustulated Unreported
6. Nut wall Free Fused Free Free Fused
7. Nut indumentum Finely adpressed silver hairs on the umbo. Finely adpressed silver hairs on the umbo. Sparsely covered with adpressed white hairs. Dense white hairs, only around umbo. Unreported.
8. Nut shape, size and scar (l × w) Rectangular and flattened at the base, 2.5–2.9 cm × 2.3–2.4 cm, scar 2.3–2.5 × 2.3–2.4 cm. Ovoid, emarginate, concave at the bottom, 1 cm × 1 cm, scar 0.2–0.3 × 1 cm. Ovoid and asymmetrically compressed, 2–3 cm × 1 cm, scar unreported. Ovoid, asymmetric and slightly curved, 3 × 1.5 cm, scar unreported. Asymmetrically depressed subglobose, 3.5–4 cm × 2–3 cm, scar basal 1 cm diam.
9. Leaf shape, size (l × w) Elliptic, with cuneate base and acute apex, (11)13–17(19) × (2)3.5–5(6) cm. Obovate, obovate-oblong, oblong or lanceolate, 7–17 × 5–7 cm. Elliptic, oblong or obovate, 10–25 × 3.2–6.3 cm. Lanceolate or oblong, 10–20 × 3–6 cm. Oblong, elliptic or obovate, 10–20 × 3.5–8 cm.

During our field survey, we encountered additional Fagaceae species, for example, Lithocarpus elegans (Blume) Hatus. ex Soepadmo, Lithocarpus wrayi (King) A.Camus, Lithocarpus cf. kingianus (Gamble) A.Camus, Lithocarpus hendersonianus A.Camus., Lithocarpus macphailii (M.R.Hend.) Barnett, Lithocarpus sundaicus (Blume) Rehder, Castanopsis inermis (Lindl.) Benth. & Hook.f., Castanopsis malaccensis and two (as of yet) unidentified species of Quercus.

Few studies have been done on Fagaceae in Peninsular Malaysia in the last decade. The discovery of C. corallocarpus in Peninsular Malaysia highlights the continued potential of new findings for this family in the region. Moreover, with only two recorded individuals of C. corallocarpus in BTFC, further assessment is needed to determine the extent of the species distribution for its conservation. This also extends to other Fagaceae species from Castanopsis and Lithocarpus in which many are data-defficient on the IUCN Red List (IUCN 2022).

Acknowledgements

This discovery was part of fieldwork conducted under LO’s Ph.D. that was funded by Yayasan Sime Darby (grant M0005.54.04) and the University of Nottingham Malaysia and subsequent work by the Southeast Asia Biodiversity Research Institute (SEABRI; grant #Y4ZK111B01). We are grateful to the Perak State Park Corporation for allowing us to carry out the collection and Tang Fook Leong from RIMAU for accommodating us in Sungai Papan. We are especially grateful to the Orang Asli field staff, Param bin Pura, Muhamad Tauhid bin Tunil and Sudin bin Tunil for their assistance when sampling. We are grateful to Forest Research Institute Malaysia for housing the Type specimen. We would also like to thank the subject editor Dr. Norbert Holstein and the two reviewers for their constructive comments.

References

  • Chen L, Li X, Zhang J, Li J (2010) Castanopsis malipoensis and C. jinpingensis (Fagaceae), two new species from Yunnan, China. Annales Botanici Fennici 47(4): 301–305. https://doi.org/10.5735/085.047.0406
  • Chen L, Zhang Z, Hu Y, Li X, Li J (2011) A new species and one new name in Castanopsis (Fagaceae) from Hainan, China. Novon: A Journal for Botanical Nomenclature 21(3): 317–321. https://doi.org/10.3417/2009103
  • Cockburn PF (1972) Fagaceae. In: Whitmore TC (Ed.) Tree Flora Malaya (Vol. 1). Longman Malaysia, Kuala Lumpur, 196–232.
  • Corner EJ (1988) Wayside Tree of Malaya (Vol.1). Malayan Nature Society, Kuala Lumpur.
  • Hoang TS, Nguyen VN, Tran LD, Vo QT, Trinh NB, Nguyen HT, Li B (2018) Castanopsis dongnaiensis (Fagaceae), a New Species from Vietnam. Annales Botanici Fennici 55(4–6): 227–231. https://doi.org/10.5735/085.055.0404
  • Kaul RB, Abbe EC, Abbe LB (1986) Reproductive phenology of the oak family (Fagaceae) in the lowland rain forests of Borneo. Biotropica 18(1): 51–55. https://doi.org/10.2307/2388362
  • Li R, Sun B, Wang Q, Ma F, Xu X, Wang Y, Jia H (2015) Two new Castanopsis (Fagaceae) species based on cupule and foliage from the upper Miocene of eastern Zhejiang, China. Plant Systematics and Evolution 301(1): 25–39. https://doi.org/10.1007/s00606-014-1051-7
  • Malaysian Nature Society (2005) MNS position statement. Kuala Lumpur, Malaysia
  • Myers N, Mittermeier RA, Mittermeier CG, Da Fonseca GA, Kent J (2000) Biodiversity hotspots for conservation priorities. Nature 403(6772): 853–858. https://doi.org/10.1038/35002501
  • Phengklai C (2008) Fagaceae (Vol. 9 (3). In: Santisuk T, Larsen K, Nielsen I, Chayamarit K, Phengkhlai C, Pedersen H, Parnell J, Middleton D, Newman M, Simpson DA, van Welzen PC, Hul S, Kato M (Eds) Flora of Thailand. The Forest Herbarium, National Parks, Wildlife and Conservation Department, Bangkok.
  • Royal Botanic Gardens Kew (2021) The World Checklist of Vascular Plants (WCVP). Checklist dataset. https://doi.org/10.15468/6h8ucr [Accessed September 2022]
  • Soepadmo E (1972) Fagaceae. Flora Malesiana Series I (Vol. 7 (2). Rijksherbarium /Hortus Botanicus, Leiden University, Leiden.
  • Yong WSY, Chua LSL, Lau KH, Siti-Nur Fatinah K, Cheah YH, Yao TL, Rafidah AR, Lim CL, Syahida-Emiza S, Ummul-Nazrah AR, Nor-Ezzawanis AT, Chew MY, Siti-Munirah MY, Julius A, Phoon SN, Sam YY, Nadiah I, Ong PT, Sarah-Nabila R, Suhaida M, Muhammad-Alif Azyraf A, Siti-Eryani S, Yap JW, Jutta M, Syazwani A, Norzielawati S, Kiew R, Chung RCK (2021) Malaysia Red List: Plants of Peninsular Malaysia Part 1, Volume 1. Aslita, Kuala Lumpur.
login to comment