Research Article |
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Corresponding author: Gabriel A. Iturralde ( gabriel.iturralde@udla.edu.ec ) Academic editor: Igor Kessous
© 2025 Marco M. Jiménez, Luis Baquero, Henry X. Garzón-Suárez, Carlos Martel, James A. Chamaya G., Nadia Lapo-González, Florian A. Werner, Gabriel A. Iturralde.
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:
Jiménez MM, Baquero L, Garzón-Suárez HX, Martel C, Chamaya G. JA, Lapo-González N, Werner FA, Iturralde GA (2025) Telipogon villonacoensis (Orchidaceae: Oncidiinae), a new species with an unexpectedly wide distribution from the northern and central Andes of South America. Plant Ecology and Evolution 158(3): 392-402. https://doi.org/10.5091/plecevo.157554
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Background and aims – Telipogon is an orchid genus with a main diversity centre located in the tropical Andes. Some small-flowered Telipogon species, formerly classified under Stellilabium, remain poorly known. During recent fieldwork in southern Ecuador, an undetermined species of a miniature Telipogon was recorded and collected. We aimed to taxonomically identify the orchid and understand its phylogenetic relationships.
Material and methods – We conducted field work in diverse parts of Ecuador and Peru, revised material deposited at various herbaria, and records available on iNaturalist. Furthermore, we extracted, amplified, and sequenced DNA sequences to evaluate the phylogenetic position of the undetermined species.
Key results – The unidentified species turned out to be an undescribed Telipogon species, which we describe and name here as T. villonacoensis. It has also been recorded in Colombia and Peru, an unusually wide distribution for a Telipogon species. Telipogon villonacoensis is distinguished by its pale green to yellow flowers, the elliptic petals and lip, minute lobes and red coloration at its basal third. This species appears to have a patchy distribution and specialized habitat preferences, growing as an epiphyte in montane shrublands and forests. Although fewer than 200 individuals have been documented so far, and its habitats face ongoing threats, our conservation assessment indicates the species could be classified as not threatened. Phylogenetic analyses resulted in a well-resolved tree, in which T. villonacoensis is placed within the clade of the South American miniature Telipogon and sister to, but genetically distinct from, T. pogonostalix, though it is morphologically more similar to T. alexii, a species placed in another subclade of South American miniature Telipogon.
Conclusion – Our results highlight the underestimated diversity and distribution range of miniature Telipogon and underscore the need for continued collaborative exploration and conservation in Andean ecosystems. These findings will contribute to a better understanding of orchid diversity and evolution of Telipogon species.
Colombia, Ecuador, new taxon, orchids, Peru, Stellilabium, taxonomy
Telipogon Kunth is a neotropical genus in the Orchidaceae that includes approximately 250 species, distributed across humid montane forests from southern Mexico throughout Central America and the Tropical Andes up to northern Bolivia (
Telipogon exhibits its highest richness, including numerous miniature species, in the tropical Andes. For instance, 10 species of miniature Telipogon species in Colombia (Martel pers. comm.), 14 species in Ecuador (Iturralde and Baquero pers. comm.), 10 species in Peru (Carlos Martel pers. comm.), and 7 species in Bolivia (
During our exploratory work over the past two years, one of the authors (MJ) found populations of one unknown species of miniature Telipogon in southern Ecuador, which underscores the rich biodiversity of the country’s montane forests and highlights the importance of continued botanical exploration in the region. Surprisingly, the same species has also been collected and recorded in Colombia and Peru by other researchers, which emphasizes the importance of collaborative work in the Neotropics. In this study, we provide a formal description of this species, accompanied by illustrations, photographs, and information on its distribution, habitat, phenology, and conservation status. Furthermore, we provide information to differentiate the new taxon from the most similar species, T. pogonostalix Rchb.f. and T. alexii N.H.Williams & Dressler.
We carried out field explorations in different areas of Ecuador and Peru between 2015 and 2024, where we found plants of the new entity. Floral and vegetative structures were photographed (i.e. Panasonic FZ300 camera with Raynox DCR-250 mm Super Macro lens, Nikon D5100 camera with an AF-S DX Micro Nikkor 40 mm f/2.8G lens, Canon A-1 camera with a Canon FD 50 mm F3.5 lens, Canon EOS Rebel T5 with a Canon 100 mm F2.8 lens). Specimens were collected and pressed as voucher material, although for some specimens, only detailed photographs were taken in situ when a single plant was spotted in the area. Flowers were preserved in a 70% ethanol, 29% water, and 1% glycerol solution. Leaf samples of specimens from Ecuador were dried in silica gel for molecular analysis. Voucher specimens were deposited in the herbaria of the Universidad Técnica Particular de Loja herbarium (
In addition, the iNaturalist platform (https://www.inaturalist.org/) was reviewed in detail in search of records of the species for other locations. We used herbarium and iNaturalist records to prepare a distribution map, generated using the software ArcGIS (GIS v.10.8: Redlands, CA: Environmental Systems Research Institute, Inc. https://www.esri.com/). We also used this database to determine the extent of occurrence (EOO) and area of occupancy (AOO) of the new entity by using the GEoCAT tool (
Figures were prepared using the software Adobe Photoshop® 2019 (San Jose, CA, USA). Plant collection was conducted under different collecting permits issued by the Ministry of Environment and Water – MAATE (No. MAATE-DBI-CM-2022-0248 and CM-2021-0187) in Ecuador, and by the Ministry of Agricultural Development and Irrigation (No. AUT-IFL-2022-051) in Peru.
A total of 23 Telipogon species were included in the phylogenetic reconstruction. DNA sequence data of six Ecuadorian species (i.e. Telipogon alexii, T. cf. alticola (Dodson & R.Escobar) N.H.Williams & Dressler, T. astroglossus Rchb.f., T. pogonostalix, T. williamsii P.Ortiz, and the undescribed species) were generated and deposited on GenBank. Additional DNA sequences of ITS and matK regions for Central and South American Telipogon species were obtained from GenBank (https://www.ncbi.nlm.nih.gov/genbank/). In addition, Hofmeisterella eumicroscopica (Rchb.f) Rchb.f. and Trichoceros antennifer (Bonpl.) Kunth, both of which belong to the Telipogon alliance (
Species list, distribution, and details of the GenBank accessions or sequenced plant vouchers for the phylogenetic reconstruction. Distribution: Alpha-2 ISO country codes. * Indicates sequenced vouchers for this study.
| Taxon | Distribution | rITS | matK |
| Fernandezia sanguinea (Lindl.) Garay & Dunst. | CO, EC, PE, VE | FJ565526 | FJ565009 |
| Hofmeisterella eumicroscopica (Rchb.f.) Rchb.f. | BO, CO, EC, PE, VE | DQ315823 | AF350589 |
| Telipogon acicularis (Dressler) N.H.Williams & Dressler | CR, PA | DQ315837 | DQ315896 |
| *Telipogon alexii N.H.Williams & Dressler | EC |
PV983249 / GI-2309-2107 ( |
PV988129 / GI-2309-2107 ( |
| *Telipogon cf. alticola (Dodson & R.Escobar) N.H.Williams & Dressler | CO, EC, PE, VE |
PV983250 / GI-2310-2608 ( |
PV988130 / GI-2310-2608 ( |
| *Telipogon astroglossus Rchb.f. | EC, PE |
PV983251 / GI-2207-4030 ( |
PV988131 / GI-2207-4030 ( |
| Telipogon ariasii Dodson & D.E.Benn. | PE | DQ315852 | DQ315902 |
| Telipogon boliviensis (R.Vásquez & Dodson) N.H.Williams & Dressler | BO | DQ315839 | - |
| Telipogon bowmanii Rchb.f. | BO, CO, EC, PE | DQ315880 | DQ315912 |
| Telipogon butcheri Dodson & R.Escobar | CR | DQ315855 | DQ315904 |
| Telipogon bombiformis Dressler | CR | DQ315854 | FJ564866 |
| Telipogon dalstromii Dodson | EC, PE | DQ315861 | DQ315906 |
| Telipogon hausmannianus Rchb.f. | EC, PE | OR689558 | OR689580 |
| Telipogon helleri (L.O.Williams) N.H.Williams & Dressler | CR | MF962882 | MF962888 |
| Telipogon hystrix (Dodson) N.H.Williams & Dressler | EC | DQ315841 | DQ315899 |
| Telipogon maduroi Dressler | PA | DQ315867 | FJ564867 |
| Telipogon pillaropatatensis Iturralde, Monteros & Baquero | EC | OR689556 | OR689582 |
| Telipogon nervosus (L.) Druce | CO | DQ315870 | DQ315907 |
| Telipogon octavioi Dodson & R.Escobar | CO | OR689559 | OR689579 |
| *Telipogon pogonostalix Rchb.f. | CO, EC, PE |
AF239392; PV983252 / GI-2211-6702 ( |
AF239488; PV988132 / GI-2211-6702 ( |
| Telipogon pulcher Rchb.f. | CO, EC | DQ315875 | DQ315910 |
| Telipogon smaragdinus (Pupulin & M.A.Blanco) N.H.Williams & Dressler | CR | DQ315844 | FJ565034 |
| Telipogon venustus Schltr. | EC, PE | FJ565183 | FJ564703 |
| *Telipogon villonacoensis M.M.Jiménez, Iturralde & C.Martel | CO, EC, PE |
PV983253 / MJ-1560 ( |
PV988133 / MJ-1560 ( |
| *Telipogon williamsii P.Ortiz | CO, EC |
PV983254 / GI-2310-2655 ( |
PV988134 / GI-2310-2655 ( |
| Trichoceros antennifer (Bonpl.) Kunth | BO, CO, EC, PE | DQ315883 | FJ564953 |
Genomic DNA was isolated following a rapid extraction procedure (
Phylogenetic analyses were conducted under both Bayesian Inference (BI) and Maximum Likelihood (ML) approaches. For the Bayesian analysis, we used BEAST v.1.10.4 (
ECUADOR – Loja • Western cordillera of the Loja basin, near Loja; 2565 m; coordinates omitted for conservation reasons; detailed data on the holotype; 21 Feb. 2023; M. Jiménez 1560; holotype:
Telipogon villonacoensis is similar to T. pogonostalix by the miniature, acaulescent habit, pale green to yellow flowers, and oblong and ecallose lip, but the first differs by its lip stained with purple-brown at the basal third, ending abruptly in an almost straight line (vs green-yellow at the base), lateral lobes of the lip ca 0.25 mm long (vs lateral lobes 1.0–1.3 mm long), the pink-purple column (vs white) with 2–7 setae per tuft, 0.2 mm long (vs 9–13 setae per tuft, 0.7–0.8 mm long), dark purple and coralloid setae with bifid to trifid apex (vs white and acicular setae with stellate apex).
Epiphytic herb, erect, ca 8 cm tall including the inflorescence. Roots 1.1–1.7 mm in diameter, thick, cylindrical, basal. Stem inconspicuous, 3–4 × 2–3 mm, surrounded by the leaf sheaths. Leaves 13–40 mm long, 2–5 per stem, subcoriaceous, distichous, articulated, decurrent, conduplicate; leaf blade 12–37 × 3–6 mm, oblong to narrowly elliptic, acute, slightly falcate, minutely and sparsely pustulose-papillose along the adaxial surface. Inflorescence up to ca 7 cm long, apical or rarely lateral, 1–2 per stem, erect, racemose, unbranched, green, with 4–10 flowers, spirally arranged, successive, rarely two open at the same time; peduncle 27–32 mm long, terete, progressively and very narrowed towards the base, sometimes with 1 amplexicaul triangular bract apically; rachis 19.3–36.2 mm long, slightly compressed, sub-verrucose, partially enveloped by the floral bracts; floral bracts 2.0–2.3 × 1.2–1.5 mm when extended, conduplicate, triangular-ovate, acute, decurrent, translucent. Ovary 3.3–3.5 long × 0.9 mm wide, light green, terete, sub-verrucose, grooved; pedicel ca 3.5 mm long. Flowers ca 6.6 × 7.4 mm, non-resupinate; sepals translucent, shallow, pale green to yellow stained with brownish purple at the base, the longitudinal mid-vein dark green to brownish; petals white or yellow, with a greenish coloration between the veins, light brown-purple at the base, veins green or brown-purple; lip white with green or brown-purple veins, the basal third stained purple-brown, ending abruptly in a straight line. Sepals subtriangular-ovate, subacute, reflexed, entire, 1-veined, membranous, papillose, sparsely verrucose abaxially; dorsal sepal 2.9–3.9 × 1.2 mm; lateral sepals 3.1–3.9 × 1.2–1.3 mm, oblique. Petals 3.4–4.7 × 1.4–1.8 mm, elliptic-oblong to elliptic-obovate, subacute, asymmetrical, entire margins, 3-veined (midvein reaching the apex, lateral veins reaching only halfway), minutely papillose, shallow, slightly incurved. Lip 3.2–4.7 × 1.5–1.6 mm, oblong-ovate, obtuse, involute at the apex, entire margins, the base partially surrounds the column, shallow in most of its length, slightly convex at the apex, surface papillose, margins retrorse ciliate, 5-veined (midvein reaching the apex, internal pair reaching the apical fourth, external pair reaching only halfway), 2-auriculate at the base; auricle 0.2 mm long, with obtuse angles. Column 1.6–1.7 long × 1.2 mm wide, terete, slightly dorsoventrally compressed, pink to purple, densely papillose, the ventral edge slightly protruding and swollen, forming a minute obtuse bump, with two sparsely dense tufts of setae on each side of the anther; setae 2–7 per tuft, up to 0.2 mm long, dark purple (rarely purely white) with white, tips, stellate or coralloid apex; stigma apical, transversely elliptic; rostellum erect; clinandrium almost straight, not hooded. Anther cap dorsal, 0.8 × 1.0 mm, widely sub-cordiform, bilocular, purple suffused with white. Pollinarium 1.5 mm long, with two pairs of unequal, narrowly ovoid pollinia, with a stipe 0.4 mm long, and an uncinate viscidium. Fruits capsule 10 × 4.7 mm, sub-triquetrous with rounded angles.
According to confirmed records in Ecuador, Telipogon villonacoensis is distributed in the inter-Andean valleys of the Loja Province and the south-eastern slope of the Andes in the Zamora Chinchipe Province, between 2350–2650 m. In Peru, it has been reported in Cajamarca, in the north, and in Cusco, in the south, between 2500 and 3000 m. However, several records on iNaturalist suggest that this species is widely distributed from west-central Colombia, through east and west Ecuador, to south-east Peru (Fig.
Telipogon villonacoensis grows as an epiphyte on small branches and twigs of trees or shrubs, which can be covered in mosses and lichens. The vegetation of the type locality reaches a maximum of 6 meters and is dominated by Clethra revoluta (Ruiz & Pav.) Spreng., Oreocallis grandiflora (Lam.) R.Br., Clusia cf. alata Planch. & Triana, Viburnum triphyllum Benth., Baccharis latifolia (Ruiz & Pav.) Pers., and Siparuna muricata (Ruiz & Pav.) A.DC. Most individuals of T. villonacoensis were found on the twigs and stems of Clethra revoluta and Clusia cf. alata; plants are less commonly found on Ceratostema loranthiflorum Benth., Cavendishia bracteata (Ruiz & Pav. ex J.St.-Hil.) Hoerold, Baccharis obtusifolia Kunth, and rarely on Arcytophyllum thymifolium (Ruiz & Pav.) Standl, Alnus acuminata Kunth, and Chaetogastra laxa (Desr.) P.J.F.Guim. & Michelang. The new species can be found near streams, roads, or grasslands. Telipogon villonacoensis grows together with Cyrtochilum macranthum (Lindl.) Kraenzl., Oncidium cruentoides M.W.Chase & N.H.Williams, Epidendrum jaramilloae Hágsater & Dodson, and Passiflora mathewsii (Mast.) Killip.
We observed flowering specimens of Telipogon villonacoensis between February and July, whereas those with capsules were observed in January, September, and November. Two colour variations have been observed in the flowers of T. villonacoensis. Individuals with opaque greenish-white flowers and paler veins sparsely suffused at the base with pink. Others have a yellow perianth with darker veins intensely stained at the base with brownish purple, especially the petals (Figs
Telipogon villonacoensis. A. Habit with a close-up of the floral bract (A1) and apical portion of the leaf (A2). B. Flower in lateral view. C. Dissected perianth. D. Column, lip, and ovary in lateral view with a close-up of the setae (D1), and ventral edge of the column (D2). E. Frontal view of the column. F. Lip with a close-up of the marginal teeth (F1) and the basal, stained region (F2). G. Anther cap and pollinarium. Plate made by Nadia Lapo-González based on the type specimen (A, C-lip, D, E, F) and on M. Jiménez, G.A. Iturralde & H. Garzón-Suárez 2190 (
Individuals of Telipogon villonacoensis from different localities. A–B. Type collection near Loja, Ecuador (M. Jiménez 1560 [
The new species is named after Cerro Villonaco, one of the highest peaks of southern Ecuador’s western Cordillera of the Loja basin and where the new species was first found. This mountain is home to patches of highly threatened evergreen montane shrub forests which harbour unique species of flora such as Passiflora brachyantha L.K.Escobar and Aphelandra villonacensis Wassh.
So far, nine localities of Telipogon villonacoensis have been identified in secondary and primary forests of the high Andes in Colombia, Ecuador, and Peru. However, only a few dozen individuals have been spotted in each locality, which were restricted to specific phorophytes. The total number of observed individuals in all the localities is around 200 plants. Unfortunately, individuals of the new species are threatened by the frequent forest fires in Ecuador and the expansion of crop areas in Ecuador and Peru. The extent of occurrence (EOO) and area of occupancy (AOO) calculations resulted in 740,746 km2 and 9,000 km2 (cell width of 2 km2), respectively. Based on these values and applying the IUCN Red List Categories and Criteria (
ECUADOR – Loja • Cerro Villonaco, cerca de la vía antigua a Catamayo; 2629 m; 22 Feb. 2024; M.M. Jiménez León, G.A. Iturralde & H. Garzón-Suárez 2190;
PERU – Cajamarca • Chota, Comunidad La Palma, Bosque La Palma; 2835 m; 10 Sep. 2024; J. Chamaya G. s.n.;
Colombia, Antioquia, Municipio de Jardín, ProAves Loro Orejiamarillo Reserve, Apr. 2023; obs. by danielmesa1 (https://www.inaturalist.org/observations/153411209).
Ecuador, Imbabura, Apuela, Siempre Verde Reserve, 28 Jan. 2021, obs. by bosquenublado (https://www.inaturalist.org/observations/68746177). Loja, Cerro Villonaco, F. Werner et al. 2253 [photo-voucher], in situ.
Peru, Cusco, Quispicanchis, Marcapata, 28 Sep. 2024, obs. by georgevf (https://www.inaturalist.org/observations/244444854, https://www.inaturalist.org/observations/244444309); Perus, Cusco, Quispicanchis, Marcapata, 3000 m, 25 Aug. 2015, obs. by C. Martel (Fig.
COLOMBIA – Boyacá • Santa María, Sendero Hyca Quye; 1400–1600 m; 13 Feb. 2025; Eugenio Restrepo & Lyndon Carvajal 483; UDBC!.
ECUADOR – Loja • Vilcabamba, Reserva El Bosque; 2214 m; 23 Feb. 2024; G. Iturralde GI-2406-2870;
BOLIVIA – Cochabamba • Carrasco, Parque Nacional Carrasco, cerca a la confluencia de los ríos Yana Mayu e Ivirizu; 1035 m; 13 Jan. 2020; M. Zárate 6892; BOLV!.
ECUADOR – Napo • Cosanga, road to Las Caucheras; 2080 m; 30 Oct. 2023; G. Iturralde GI-2309-2112;
The reconstructed phylogenetic trees obtained with rITS, matK, and the combined datasets showed similar topology, both with BI and ML analyses, therefore we will focus on the results using the combined dataset tree. The combined data matrix in both BI and ML analyses retrieved trees with identical topologies (ML score = -lnL 7475.35936; Fig.
Reconstructed phylogenetic tree of concatenated markers rITS and matK to evaluate the position of Telipogon villonacoensis within Telipogon. The tree on the left is based on Bayesian inference (BI) analysis (numbers at side of nodes represent posterior probability values). The tree on the right is based on Maximum Likelihood (ML) analysis (numbers at the side of nodes represent bootstrap values). Abbreviation of the genera as follows: F = Fernandezia, H = Hofmeisterella, Tr = Trichoceros, T = Telipogon. Scale bars represent the mean number of nucleotide substitutions per site.
The topologies of our reconstructed phylogenetic trees are consistent with those previously published (
Telipogon villonacoensis shares morphological characteristics with T. pogonostalix and T. alexii, both from Ecuador. The three species are characterized by plants without evident pseudobulbs; flowers with glabrous, elliptic to obovate petals; the auriculate (auricle much smaller) lip with retrorse-ciliate margins; the column terete with only two lateral tufts of bristles of varying sizes (column dorsally bristleless) (Fig.
Telipogon villonacoensis is easily distinguished from T. pogonostalix by the brown-purple colouration at the basal half of the lip (vs yellow-green lip) with a purple column (vs white column) and very short auriculae at the lip base (vs falcate auricle).
Although the new taxon resembles T. alexii morphologically, as they both have dark purplish flowers with purple columns and small auriculae at the lip base, the phylogenetic analyses indicate they are not too closely related.
Telipogon villonacoensis differs from T. alexii by the white to light yellow petals (vs cream-pinkish at the base and yellowish toward the apex), the elliptic-oblong to elliptic-obovate petals with subacute apex (vs narrowly ovate, long attenuate at the apex), lip 5-veined and brown-purple at the basal half (vs 3-veined and cream-pinkish lip), and column with 2–8 well-developed setae (vs column glabrous or with 2–4-minute setae) (
The distribution of T. villonacoensis overlaps with that of some other miniature Telipogon species, which have some resemblances with the general pattern of the flower and the general shape of the petals and lip, such as the Ecuadorian T. jostii (Dodson) N.H.Williams & Dressler, the Peruvian T. selbyanus N.H.Williams & Dressler, and the Bolivian T. perlobatus (Senghas) N.H.Williams & Dressler. Supplementary material
The authors are indebted to Jorge Armijos, Wilson Raura, and Michael Burghardt for their valuable collaboration during this investigation. We thank Eugenio Restrepo and Daniel Mesa for providing information on Colombian specimens and Byron Freire for laboratory assistance. MMJ, GAI, and LB thank the Universidad de Las Américas (UDLA) for funding orchid research in Ecuador, grant No. 527.A.XV.24. We acknowledge the Universidad Técnica Particular de Loja herbarium (
Comparison between Telipogon villonacoensis and other miniature Telipogon species.