Abstract
Typhoniumvinicolor from Khon Kaen Province (Northeastern Thailand), is described and illustrated as a species new to science. Color plates, phenology, distribution, discussion of similar taxa, and conservation status assessment are provided.
Key words: Areae, Aroideae, Indochina, Northeastern Thailand, plant taxonomy
Introduction
TyphoniumSchott (1829) (Araceae Juss.) is a genus of tuberous (sometimes rhizomatous or stoloniferous), terrestrial, and seasonally dormant herbs that inhabit forest floors, rocky areas, wet sites, stream sides, and grassy places in tropical and subtropical humid and seasonal forests, as well as in agricultural land (Mayo et al. 1997; Low et al. 2020). Hay et al. (2022) transferred most of the Australian Typhonium species to Lazarum A.Hay, so, according to these authors Typhonium (sensu stricto) would refer to species mainly distributed in Indochina (see e.g., Low et al. 2020; Hay and Hein 2022). Among the genera of tribe Areae, Typhoniums.str. is the largest one, with more than 70 species (100 based on Boyce and Croat 2011; 72 in POWO 2024). The highest species diversity of Typhonium is found in Thailand, with 32 species, 24 of which are endemic (Boyce et al. 2012). Later than Boyce et al. (2012), six new species have been described from Thailand (Galloway 2012, 2015; Hetterscheid 2013; Sookchaloem and Maneeanakekul 2018), increasing the total number of species in the country to 38. However, the current number of species occurring in Thailand is undoubtedly much higher (Boyce et al. 2012).
During our botanical survey in Khon Kaen Province (Northeastern Thailand), an unknown species of Typhonium was collected by the second author (SS). After meticulously examining its morphology and comparing it with protologues and relevant literature, as well as with digitized type specimens from Thailand and neighboring countries, it became apparent that the collected specimen does not match any other known Typhonium species. Thus, we consider it to represent a taxonomic novelty, which is described and illustrated in the present paper.
Materials and methods
The measurements and descriptions were based on freshly collected and/or alcohol-preserved material, processed according to the methods established by Davies et al. (2023). The species description follows Hay and Hein (2022), while Araceae morphological terminology follows Mayo et al. (1997) implemented by the descriptive terminology of Beentje (2016). Relevant type specimens of Typhonium species from Thailand and neighboring countries were examined in different herbaria (A, AAU, B, BK, BKF, C, CAL, CMU, E, HITBC, K, KKU, KUN, L, M, MO, P, PE, QBG, SING, and WAG; acronyms follow Thiers 2024) through high-resolution images from https://plants.jstor.org/ and Global Biodiversity Information Facility (GBIF) accessed from https://www.gbif.org. An assessment of conservation status was carried out following IUCN (2024), based on our current knowledge and the respective terminology on categories, criteria, and subcriteria. The photographs in the plate were taken with an iPhone 13 (iOS version 17.5.1, 2021, Apple Inc., Cupertino, CA, USA). The figure in this study was created using Pixelmator Pro (Version 3.6.5, Archipelago, 2023, Pixelmator Team, Vilnius, Lithuania) on a MacBook Pro (13-inch, M1, 2020, Apple Inc., Cupertino, CA, USA).
Taxonomic treatment
. Typhonium vinicolor
P.Saensouk, K.Z.Hein & Saensouk sp. nov.
F11E32F7-7B4C-58DE-9C5D-E0728A1BF694
urn:lsid:ipni.org:names:77347851-1
Figure 1.
TyphoniumvinicolorA plant in habitat B excavated flowering plants C leaf blade (left showing adaxial surface, right showing abaxial surface) D inflorescence at pistillate anthesis, nearside spathe artificially removed E spadix at pistillate anthesis, nearside spathe artificially removed. Photos by: Surapon Saensouk and Thawatphong Boonma.
Type.
Thailand • Northeastern – Khon Kaen Province, 13 May 2023, Surapon Ara001 (holotype KKU!; isotypes FOF!, MSU!).
Diagnosis.
Typhoniumvinicolor is easily distinguishable from the other Typhonium species by having narrowly elliptic to elliptic-lanceolate leaf blades with a reddish-purple abaxial surface. An only exception is T.laoticum Gagnep. (Gagnepain 1942), which shows similar leaf blades. However, T.vinicolor differs from T.laoticum by its reddish-purple abaxial surface of leaf blades (vs. pale green), white or pale green spathe with dark purple mottling externally (vs. pink spathe with brown mottling externally), pistillate zone with 5–6 pistil rows (vs. 2–3 pistil rows), and staminodes more or less loosely arranged in 4–5 spirals (vs. staminodes densely arranged in 2–3 spirals).
Description.
Small, deciduous, herbs, to 15 cm tall. Stem hypogeal, subglobose or depressed globose tuber, 1.2–1.5 cm in diameter, externally pale brown, internally white. Roots filiform, 0.6–1.0 mm in diameter, white. Leaves 1–2(–3) together; petioles 6.5–8.5 cm long, ca. 0.2 cm in diameter, erect, slender, terete, glabrous, basal subterranean portion white, upper aerial portion pale green with numerous longitudinal dark purple striations and spots; petiolar sheath 2.5–3.0 cm long, ca. 1/3 of petiole length; leaf blade 8.0–13.0 × 1.8–4.2 cm, narrowly elliptic to elliptic-lanceolate, or elliptic-oblanceolate, chartaceous, adaxially medium green, abaxially reddish-purple, glabrous on both sides, base cuneate or obtuse, margin entire, apex acute and mucronate, mucro ca. 1 mm long; midrib adaxially impressed, abaxially raised, rounded, 1.5–1.8 mm wide at the base, ca. 1.0 mm wide at center, then narrowing towards blade apex; primary lateral veins 5–7 per side, adaxially impressed, abaxially raised, diverging from the midrib at 15–30°, anastomosing at 0.5–1.5 mm from margin into an intramarginal collective vein; higher order venation reticulate. Inflorescence solitary, subtended by a cataphyll; cataphyll up to 3.0 cm long, linear-lanceolate, membranous, semi-hyaline, greenish white or white, later withering brown; peduncle 2.8–3.2 cm long, ca. 0.2 cm in diameter, almost entirely subterranean, white, terete, glabrous; spathe 8.5–9.5 cm long, strongly differentiated into a spathe tube and a spathe limb by a constriction; spathe tube ca. 1.2 cm long, 0.6–0.7 cm in diameter, convolute, ellipsoid-ovoid, externally white or greenish white with a dense dark purple mottling, internally greenish white; spathe limb 7.3–8.3 cm long, 0.6–0.7 cm in diameter at base, linear-lanceolate, tapering towards apex, externally green or yellowish-green with dark purple mottling, internally pale yellowish green, basal part of limb shortly convolute and erect, upper part reflexed and then strongly coiled at anthesis, apex narrowly acute. Spadix sessile, 8.0–9.0 cm long, nearly as long as or shorter than spathe; pistillate zone ca. 2 mm long, ca. 3 mm in diameter at the base, shortly conical, with 5–6 rows of congested pistils; ovary ca. 0.7 mm high, ca. 0.5 mm in diameter, obovoid, white, unilocular with one basal ovule held obliquely on a funicle, on a basal placenta; style very short, ca. 0.1 mm high, ca. 2.5 mm in diameter; stigma ca. 0.3 mm in diameter, discoid, red, papillate; sterile interstice between pistillate and staminate zones 0.8–1.0 cm long, ca. 0.1 cm in diameter, upper part naked, terete, glabrous, glossy white, lower ca. 0.2 cm covered with 4–5 spirals of staminodes; staminodes 1.2–1.5 mm long, 0.5–0.7 mm in diameter at widest point, clavate-fusiform, shortly beaked with acute apex, free, slightly distant from each other, perpendicular to the spadix axis or slightly curved downwards, glabrous, yellow; staminate zone 0.7–1.0 cm long, ca. 0.3 cm in diameter, cylindric; stamens congested, not ostensibly arranged into staminate flowers, irregularly 4-lobed, 0.6–0.7 mm in diameter, pink or yellow, dehiscing by an apical pore; appendix sessile, 6.2–7.0 cm long, 1.5–2.0 mm in diameter, narrowly elongate-conical, tapering towards apex, erect or weakly arching, glabrous, ivory-colored, base slightly attenuate, apex acute. Infructescence not seen.
Etymology.
The specific epithet is derived from the Latin “vinicolor” (wine-coloured), referring to the reddish-purple abaxial surface of the leaves.
Proposed vernacular name.
Uttapit-See-Wine.
Phenology.
Flowering time in May.
Distribution and habitat.
The newly discovered species is found exclusively at its type locality in Khon Kaen Province (Northeastern Thailand). It thrives in shaded to semi-shaded areas of tropical deciduous forests at elevations ranging from 200 to 250 m a.s.l. The species shows optimal growth in sandy loam soil mixed with rocks.
Conservation status.
This new species is known exclusively from its type locality, and no sufficient information there is regarding potential threats to its habitat. In accordance with the Red List criteria of the IUCN Standards and Petitions Subcommittee (2024), we propose classifying this species as ‘Data Deficient’ (DD). Further research is necessary, as there is inadequate information to assess the conservation status of this species. Currently, data is limited regarding its distribution, with no details on population size, trends, or potential threats to its habitat.
Taxonomic notes.
Based on overall morphology, this new species is also similar to Typhoniumgriseum Hett. & Sookch. (Hetterscheid et al. 2001), which is a sister species of T.laoticum (Low et al. 2020). But T.vinicolor is strikingly different from T.griseum in having the leaf blade base cuneate or obtuse (vs. with rounded posterior lobes), spadix nearly as long as, or shorter than, spathe (vs. longer than spathe), clavate-fusiform and yellow staminodes (vs. narrowly fusiform, sickle-shaped, white staminodes), longer staminate zone (ca. 1 cm vs. ca. 0.5 cm long), and erect or weakly arching, ivory-colored appendix (vs. strongly arching, pale brown appendix).
Regarding spathe and spadix structures, the new species also resembles Typhoniumhuense V.D.Nguyen & Croat (Nguyen and Croat 1997), T.lineare Hett. & V.D.Nguyen (Hetterscheid and Nguyen 2001) and T.stigmatilobatum V.D.Nguyen (Nguyen 2008) from Vietnam. However, the latter three species differ from T.vinicolor by having horizontally flexed spathe limb at anthesis (vs. only the upper part of spathe limb reflexed and then strongly coiled at anthesis in T.vinicolor) and strongly arching, dark brown or violet, stipitate appendix (vs. erect or weakly arching, ivory, sessile appendix in T.vinicolor). A more detailed comparison between T.vinicolor and its morphologically allied species is presented in Table 1.
Table 1.
Morphological comparison of Typhoniumvinicolor and its allied species, T.griseum (Hetterscheid et al. 2001), T.huense (Nguyen and Croat 1997), T.laoticum (Gagnepain 1942; Boyce et al. 2012), T.lineare (Hetterscheid and Nguyen 2001) and T.stigmatilobatum (Nguyen 2008).
T.griseum | T.huense | T.laoticum | T.lineare | T.stigmatilobatum | T.vinicolor | |
---|---|---|---|---|---|---|
Leaf blade | orbicular, triangular cordate or narrowly ovate | triangular-cordate to deeply trilobed | lanceolate or elliptic-oblong | pedatisect with linear or linear-lanceolate lobes | deeply trilobed or pedatisect with ovate to oblong-ovate lobes | narrowly elliptic to elliptic-lanceolate |
Spathe tube | ca. 1 cm long, externally dirty white with brownish-red spots | ca. 1.5 cm long, externally pale green with purplish violet spots | 1.3–1.5 cm long, externally pink with brown striations and spots | up to 1.8 cm long, externally whitish-gray with blackish-gray striations and spots | ca. 1.3 cm long, externally pale green or dull white with black or brown spots | ca. 1.2 cm long, externally white or greenish-white with a dense dark purple mottling |
Spathe limb | ca. 10 times longer than spathe tube |
ca. 6 times longer than spathe tube |
4–5 times longer than spathe tube |
7–8 times longer than spathe tube |
10–12 times longer than spathe tube |
6–7 times longer than spathe tube |
Spadix | longer than spathe, ca. 13 cm long | as long as or slightly longer than spathe, up to 11 cm long | shorter than the spathe, ca. 7 cm long | as long as or slightly shorter than spathe, up to 17 cm long | as long as spathe, up to 17 cm long | nearly as long as or shorter than spathe, 8.0–9.0 cm long |
Staminodes | narrowly fusiform, sickle-shaped, curved downwards, white | fusiform, variously directed, yellowish white | clavate, perpendicular to the spadix axis or curved upwards, white | subulate or fusiform, variously directed, white or yellow | fusiform, perpendicular to the spadix axis or slightly curved downwards, dull white | clavate-fusiform, perpendicular to the spadix axis or slightly curved downwards, yellow |
Appendix | sessile, ca. 12 cm long, strongly arching, pale brown | stipitate, ca. 9 cm long, strongly arching, brown or violet | sessile, ca. 5 cm long, erect, pale brown | stipitate, ca. 15 cm long, strongly arching, brown or golden yellow | sessile, 14–15 cm long, strongly arching, dark brown | sessile, 6.2–7.0 cm long, erect or weakly arching, ivory-colored |
Additional specimens examined (paratypes).
Thailand • Northeastern – Khon Kaen Province, 18 May 2024, Saensouk, Boonma & Sengthong, SS 24518 (FOF!).
Supplementary Material
Acknowledgments
The third author (KZH) is grateful to Alistair Hay for his expert advice and guidance in aroids research.
Citation
Saensouk P, Saensouk S, Hein KZ, Boonma T, Sengthong A, Rakarcha S (2024) Studies on Typhonium (Araceae) of Thailand I: Typhonium vinicolor, a new species from Khon Kaen Province, Northeastern Thailand. PhytoKeys 246: 189–195. https://doi.org/10.3897/phytokeys.246.128778
Funding Statement
This research was financially supported by Mahasarakham University
Additional information
Conflict of interest
The authors have declared that no competing interests exist.
Ethical statement
No ethical statement was reported.
Funding
This research was financially supported by Mahasarakham University.
Author contributions
Conceptualization PS, SS, and KZH; Data curation PS, SS, KZH, TB; Formal analysis PS, SS, KZH; Funding acquisition SS; Investigation SS, TB, and AS; Methodology PS, SS, KZH, and TB; Project administration PS and SS; Resources SS, TB, and AS; Supervision SS; Validation PS, SS, KZH, and TB; VisualizationPS, SS, KZH, and TB; Writing - original draft KZH and TB; Writing - reviewing and editing PS, SS, KZH, TB, AS, and SR.
Author ORCIDs
Surapon Saensouk https://orcid.org/0000-0002-9178-188X
Khant Zaw Hein https://orcid.org/0000-0002-8735-9264
Thawatphong Boonma https://orcid.org/0000-0003-2324-4967
Data availability
All of the data that support the findings of this study are available in the main text.
References
- Beentje H. (2016) The Kew plant glossary: an illustrated dictionary of plant terms. 2nd edn. Royal Botanic Garden, Kew, 184 pp. [Google Scholar]
- Boyce PC, Croat TB. (2011) The Uberlist of Araceae, totals for published and estimated number of species in aroid genera. http://www.aroid.org/genera/140601uberlist.pdf [Retrieved 25 May 2024]
- Boyce PC, Sookchaloem D, Hetterscheid WLA, Gusman G, Jacobsen N, Idei T, Nguyen VD. (2012) Araceae. Flora of Thailand 11: 101–321. [Google Scholar]
- Davies NMJ, Drikell C, Utteridge TMA. (2023) The Herbarium Handbook. Royal Botanic Gardens, Kew, 290 pp. [Google Scholar]
- Gagnepain F. (1942) Aracées. In: Lecomte H (Ed.) Flore générale de l’Indo-Chine 6: 1075–1196. Paris.
- Galloway A. (2012) New Araceae species from Laos and Thailand. Aroideana 35: 51–64. [Google Scholar]
- Galloway A. (2015) Two new Typhonium species from Laos and Thailand. Aroideana 38: 8–12. [Google Scholar]
- Hay A, Hein KZ. (2022) A new combination and new synonyms for Sauromatum Schott (Araceae—Areae) of northeastern India and Bangladesh. Aroideana 45(3): 148–159. [Google Scholar]
- Hay A, Barrett MD, Hetterscheid WLA. (2022) New combinations in resurrected Lazarum A.Hay (Araceae—Areae). Aroideana 45(3): 133–137. [Google Scholar]
- Hetterscheid WLA. (2013) New Typhonium species from Asia. Aroideana 36: 93–97. [Google Scholar]
- Hetterscheid WLA, Nguyen VD. (2001) Three new species of Typhonium (Araceae) from Vietnam. Aroideana 24: 24–29. [Google Scholar]
- Hetterscheid W, Sookchaloem D, Murata J. (2001) Typhonium (Araceae) of Thailand: New species and a revised key. Aroideana 24: 30–55. [Google Scholar]
- IUCN (2024) The Guidelines for Using the IUCN Red List Categories and Criteria, Version 16 (March 2024). https://nc.iucnredlist.org/redlist/content/attachment_files/RedListGuidelines.pdf [Retrieved 28 May 2024]
- Low SL, Yu CC, Ooi IH, Eiadthong W, Galloway A, Zhou ZK, Xing YW. (2020) Extensive Miocene speciation in and out of Indochina: The biogeographic history of Typhoniumsensu stricto (Araceae) and its implication for the assembly of Indochina flora. Journal of Systematics and Evolution 59(3): 419–428. 10.1111/jse.12689 [DOI] [Google Scholar]
- Mayo SJ, Bogner J, Boyce PC. (1997) The genera of Araceae. Kew: Royal Botanic Gardens, 370 pp. 10.1007/978-3-662-03531-3_7 [DOI]
- Nguyen VD. (2008) Typhoniumstigmatilobatum (Araceae tribe Areae), a new species from Vietnam. Kew Bulletin 63(3): 491–493. 10.1007/s12225-008-9044-8 [DOI] [Google Scholar]
- Nguyen VD, Croat TB. (1997) A new species of Typhonium (Araceae) from Vietnam. Aroideana 20: 48–52. 10.2307/4110401 [DOI] [Google Scholar]
- POWO (2024) Plants of the World Online. Facilitated by the Royal Botanic Gardens, Kew. http://www.plantsoftheworldonline.org/ [Retrieved 25 May 2024]
- Schott HW. (1829) Für Liebhaber der Botanik. Wiener Zeitschriftfür Kunst, Litteratur. Theater und Mode 3: 732.
- Sookchaloem D, Maneeanakekul S. (2018) Typhoniummuaklekense sp. nov. (Araceae) from Thailand. Nordic Journal of Botany 36(5): e01619. 10.1111/njb.01619 [DOI]
- Thiers BM. (2024) Index Herbariorum: a global directory of public herbaria and associated staff. New York Botanical Garden’s Virtual Herbarium. http://sweetgum.nybg.org/science/ih/ [Accessed 11 August 2024]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
All of the data that support the findings of this study are available in the main text.