Research Article |
Corresponding author: Francisco Tobar Suarez ( pacotobar76@hotmail.com ) Academic editor: Vincent Droissart
© 2021 Francisco Tobar Suarez, María Fernanda López, María José Gavilanes, Marco Federico Monteros, Tatiana Santander García, Catherine Helen Graham.
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:
Suarez FT, López MF, Gavilanes MJ, Monteros MF, García TS, Graham CH (2021) Three new endemic species of Lepanthes (Orchidaceae, Pleurothallidinae) from the highlands of Ecuador. PhytoKeys 180: 111-132. https://doi.org/10.3897/phytokeys.180.62671
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Three new species of Lepanthes from Ecuador are described and illustrated. These additions to the Ecuadorean flora were recorded in evergreen montane forest and páramo as part of three different research projects conducted during the last five years (2016–2021). Lepanthes oro-lojaensis was discovered in the southwest of El Oro province and is similar to L. jimburae, differing mainly in the much smaller plants, inflorescences and floral parts. Lepanthes microprosartima from the western slopes of Pichincha volcano in northern Ecuador resembles L. obandoi but differs in the coloration of the leaves, the inflorescence that are shorter than the leaves and the smaller floral appendix. Lepanthes caranqui, found in eastern Pichincha and Imbabura, is most similar to L. pachychila but differs from it in its much larger plants and different shape of the petals and the floral appendix. Preliminary assessments of the conservation status of the three taxonomic novelties are provided, using the IUCN Red List Categories and Criteria.
El Oro, endemism, evergreen montane forest, Imbabura, Lepanthes caranqui, Lepanthes microprosartima, Lepanthes oro-lojaensis, páramo, Pichincha
Pleurothallidinae Lindl., with over 12,000 names published and around 5,100 currently accepted species, is the largest orchid subtribe worldwide (
Three new species: Lepanthes microprosartima Tobar & M.J.Gavil., Lepanthes caranqui Tobar & Monteros and Lepanthes oro-lojaensis Tobar & M.F.Lopez are described and illustrated here. These additions belong to the subgenus Lepanthes, sect. Lepanthes, which contains more than 243 spp. in Ecuador, and thus by far the largest in the genus (
These novelties were discovered and collected as part of three different research projects conducted during the last five years (2016–2021), including “The Ecology of Plant and Hummingbird Interactions Project (EPHI),” carried out in the western slopes of Pichincha province; “El Oro Biodiversity Project,” conducted in southwestern Ecuador; and the “Floristic Inventory of La Carboneria forest remnant,” in eastern Imbabura and Pichincha provinces. The discovery of these new species demonstrates the importance of continuing the botanical exploration of a mega-diverse and incompletely inventoried country such as Ecuador.
Plants were photographed in situ and subsequently pressed and dried, and deposited at QCA and QCNE (acronyms according to
We assess the extinction risk of the three species following the
This species is similar to Lepanthes jimburae Luer & Hirtz, but can be distinguished by the smaller plants that are less than 3 cm tall (vs. up to 4 cm tall); the shorter inflorescence that is less than 4 cm long (vs. inflorescence up to 10 cm long), the shorter dorsal sepal with a shorter sepaline tail (6.0 mm vs. 9.0 mm long), the apical lobe of the petals ovate and lower lobe triangular-oblong (vs. petals with subequal, obliquely triangular, acute lobes).
Lepanthes oro-lojaensis A habit B flower C dissected sepal and petals D anther dorsal and ventral view E polinarium F dorsal view of the spread-out lip with dorsal view of the column G dorsal view of the spread-out lip without the column H lateral view of the ovary, lip and column. Drawn by F. Tobar & S.Tobar from the plant that served as type (Tobar et al 1648).
Ecuador. El Oro, Zaruma, Salvias, near Cerro de Arcos, -3.06963333°N, -79.478944°W, 3500 m, 28 Aug 2015, Tobar, Gálvez & Obando 1648 (holotype: QCNE; isotype: QCA).
Epiphytic, caespitose herbs up to 3 cm tall. Roots flexuous, cylindrical 0.7 mm in diameter. Rhizome inconspicuous. Ramicaul arcuate to pendulous, 0.9–1.9 × 0.1–0.3 cm long, with 3–4 internodes, covered entirely by light brown minutely puberulent lepanthiform sheaths with a minutely pubescent, acuminate ostium. Leaves dark-green suffused with purple, arcuate 1.0–1.3 × 0.4–0.6 cm, coriaceous, elliptic, subacute to obtuse, tridentate at the apex, base cuneate, contracted into a petiole 2–4 mm long. Inflorescence racemose, one per stem, longer than the leaf, 2.0–3.5 cm long, flexuous, producing 3–16 widely spaced, successively opening flowers; peduncle filiform, 1–3 mm long, surrounded at the base by a bract 1.5 mm long. Floral bracts sub-distichous, infundibuliform, longapiculate. Ovary 1.5 mm long, obpyramidal, slightly arcuate, irregularly keeled. Flowers ca. 12 × 4 mm; dorsal sepal red with a yellow margin, lateral sepals yellow suffused with red around the middle vein; petals with the upper lobe red and the lower one yellow, lip reddish with yellow tips, column reddish, with white and red anther. Dorsal sepal glabrous, slightly concave, ovate, ending in a decurved cauda, 3–veined, 6.0 × 2.7 mm including the cauda. Lateral sepals glabrous, with minutely denticulate margins, connate on their basal one-third, ovate, caudate, 2–veined, 5.0 × 2.0 mm. Petals, bilobate, microscopically pubescent; apical lobe ovate, rounded, lower lobe triangular-oblong, acute, ca. 3.5 × 0.9 mm. Lip bi-laminate, blades ovate, convex, subacute at the base and rounded at the apex, microscopically pubescent, covering most of the column, ca. 1.8 × 0.7 mm; the base of the lip fused to the ventral part of the column, the connectives shortly cuneate, the sinus narrowly oblong with very small, triangular, microscopically pubescent appendix. Column claviform, arcuate, markedly broaden above the middle, truncate at the apex, ca. 1.6 × 0.8 mm. Pollinarium with two ovoid pollinia, with a round, drop-like viscidium. Anther dorsal, deltate. Stigma ventral, horseshoe-shaped. Rostellum minute, apiculate. Capsule globose, 4 × 3 mm.
Lepanthes oro-lojaensis is known from a single locality on the border between El Oro and Loja provinces (Fig.
The species was collected in bloom in August and had inflorescences in different stages of development, which suggests that the flowering period may be much broader.
Lepanthes oro-lojaensis, is known only from the type location, and only two mature individuals were observed. After its discovery in 2015, two additional visits were conducted to explore surrounding areas but it was not possible to find more plants. However, it was evident that the original habitat is under strong pressure due to cattle ranching, the collection of remaining shrubs as firewood and a rapid transformation and fragmentation of the surrounding landscape due to fires and exotic species plantations such as Pinus radiata D.Don (
Morphologically, the most similar species is Lepanthes jimburae (Fig.
Similar in habit to Lepanthes obandoi Tobar & M.F. López, but distinguished by the inflorescence shorter than the leaf (vs. Inflorescence longer than) and petals with unequal triangular lobes (vs. lobes lanceolate-oblong, subequal). Lepanthes mirador Luer & Hirtz is also similar, differing from it in the superposed, arcuate secondary stems (vs. secondary stems erect, not superposed), leaf light green on the underside (vs. dark purple underside), and the tiny, oblong-lanceolate appendix (vs. appendix oblong with bilobed apex).
Lepanthes microprosartima A habit B flower C dissected sepal and petals D dorsal view of the spread-out lip whitout the column E lateral view of the ovary, and lip F lateral view of the ovary and column G ventral view of the column showing the horse-shaped stigma Drawn by M. Gavilanes from the plant that served as type (Tobar et al. 3357).
Ecuador. Pichincha, Nono, Yanacocha Reserve, masked trogon path, 0.122416°N, -78.590283°W, 3530 m, 25 Nov 2018, Tobar & Angulo 3357 (holotype: QCA-spirit; isotypes: QCNE, HPUCESI-spirit).
Terrestrial, caespitose, prolific herbs up to 40 cm in height. Roots flexuous, cylindrical, pink with yellow apex. Ramicauls arcuate, new stems arise from the apex of the old ones superposed, 4.1–25.0 × 0.2–0.3 cm long, with 4–16 internodes, covered completely by lepanthiform sheaths, these light brown, 0.3–2.9 cm long, the ostium microscopically muricate, acuminate. Leaves arcuate, 7.5–9.4 × 1.1–2.2 cm, blades oblong-ovate, light to dark green, minutely serrate along the margin, long-acuminate apically, base cuneate, contracted into a petiole 4–7 mm long. Inflorescence one per stem, shorter than the leaf, 2.5–6 cm long, borne on the underside of the leaf, racemose; peduncle filiform, 2 mm long, ca. 0.5 mm in diameter, surrounded by a basal bract. Floral bracts 2 mm long, papiraceous, obliquely infundibuliform, glabrous and long-apiculate. Ovary 3.2 mm long, obpyramidal, with irregular keels. Flowers ca. 4.5 × 13 mm; sepals entirely yellow, petals yellow with edges slightly suffused with red or pink; lip yellow with the base and edges of the blades red or pink; column pink or purple and anther purple with two yellow spots at the base. Sepals with minutely denticulate margins, dorsal sepal 6 × 4.5 mm, broadly ovate-triangular, minutely denticulate, shortly acuminate, 3-veined; lateral sepals 7 × 2.4 mm long, connate to their middle, obliquely ovate with divergent acute-acuminate apex, 2-veined. Petals ca. 3 × 1.4 mm long, 1-veined, minutely pubescent, transversely bilobed, the upper lobe narrowly triangular with revolute margins, the lower lobe smaller, broadly triangular, obtuse. Lip bi-laminate, the blades minutely pubescent, ovate, rounded, close to each other in their proximal part and divergent at the apex, ca. 1.4 ×1.2 mm; connective short, deeply cuneate, the base of the lip connate with the base of the column, sinuous, obtuse; appendix tiny, oblong-lanceolate, pubescent at the apex. Column slightly arcuate, slightly broadened apically, somewhat compressed dorsoventrally, ca. 1.2 × 0.8 mm; clinandrium covering the lower half of the anther. Anther dorsal, stigma ventral, horseshoe-shaped. Rostellum minutely triangular, yellow. Capsule ovoid 6-ribed ca. 4 × 6 mm, with persistent perianth. Capsule ellipsoid, 6-ribed.
Lepanthes microprosartima A plant growing in its natural habitat B front view of the flower C lateral view of the lip showing the apêndix D detail of the fruit E lateral view of the petal showing the revolute apex F detail of the leaf margin, minutely denticulate G anther dorsal view H anther ventral view I polinarium. Photograph by Francisco Tobar from the plant that served as type (Tobar et al. 3357).
Paratypes Ecuador. Pichincha, Nono, Reserva Verdecocha, Verdecocha: Transecto de Aves y Conservación en Reserva Verdecocha, -0.118420°N, -78.597470°W, 3400 m, 06 Feb 2018, Tobar, Santander & Hipo 3130 (QCA); Nono, Yanacocha Reserve, sendero hacia la Reserva Verdecocha 500 metros al suroeste de los bebederos de colibríes, 0.118420°N, -78.597470°W, 3810 m, 07 May 2018, Tobar 3359 (QCA).
This species is endemic to the Yanacocha and Verdecocha reserves on the western slopes of Volcán Pichincha (Fig.
The species was collected in flower in November, February and May, which suggests that flowering occurs throughout the rainy season, from October to the end of May.
From the Greek μικρό, small and προσάρτημα, appendix, in reference to the tiny appendix of this species.
Only three collecting sites have been found during three years of monitoring at two locations: Yanacocha and Verdecocha reserves (Fig.
The closest species are Lepanthes mirador (Fig.
Similar to Lepanthes pachychila Luer & Hirtz, differing in the taller plants up to 40 cm long (vs. less than 20 cm tall), the petals with narrowly triangular-oblong lobes (vs. lobes triangular), the lip with the blades thin, ovate-oblong, the base rounded and apically acute (vs. lip blade thick, broadly ovate with basal and apically rounded ends) and appendix triangular in dorsal view, with two protuberances on the top and a minute tuft of hairs at the base (vs. minutely bilobulate appendix).
Ecuador. Pichincha, Cayambe, Olmedo, El Chalpar, 5 km northwest of the San Marcos Lagoon, 3500 m, 00.15211°N, -78.00220°W, 20 Jul 2019, Tobar, Jaramillo, Correa & Monteros 3348 (holotype QCA, spirit; isotypes QCNE, HPUSECI).
Terrestrial, caespitose, prolific herbs up to 40 cm in height. Roots flexuous, cylindrical, deep pink. Ramicauls arcuate or pendulous, with 6–12 internodes, 4–22 × 0.2–0.8 cm long, covered completely by lepanthiform sheaths, these light brown, papillose, 0.5–2.5 cm long, the ostium microscopically muricate, acuminate. Leaves arcuate, slightly concave, 3.5–9.0 × 0.8–2.4 cm, blades ovate to oblong, light to dark green, long-attenuate, tridenticulate apically, base cuneate, contracted into a petiole 1–3 mm long. Inflorescence 1.0–5.6 cm long, shorter than the leaves, racemose, densely flowered, one or six per stem, producing one or two successively opening flowers; peduncle filiform, 1.0–1.5 mm long, surrounded by a basal bract. Floral bracts 2 mm long, distichous, glabrous, apiculate. Ovary 3 mm long, obpyramidal, with 6 irregular keels. Flowers ca. 13 × 8 mm; sepals minutely denticulate, entirely light yellow; petals pubescent, yellow with proximal part of the upper lobe red to brown, lip minutely pubescent white with yellow, with the base and edges of the blades purple or brown, column pink and yellow, anther white with purple apex. Dorsal sepal 7.0 × 5.0 mm, broadly ovate, shortly acuminate, 3-veined. Lateral sepals 2-veined, 6.0 × 4.0 mm, connate at least on their proximal two-thirds, obliquely ovate with divergent, shortly acuminate apices. Petals 1-veined, ca. 4.5 × 1.5 mm, transversely bilobed, lobes subequal, narrowly triangular-oblong, rounded. Lip with blades ovate-oblong, microscopically pubescent, close to each other in their proximal part and divergent at their apices, not covering the column, base of the blades rounded, apical part acute, incurved, ciliate, ca. 2.0 × 1.6 mm; connective broadly cuneate, minutely pubescent, its body connate with the base of the column, sinus obtuse, with a small, rounded, pubescent appendix, which has two protuberances on the top and a minute tuft of hairs. Column claviform, straight, ca. 2.0 × 0.8 mm; clinandrium covering only the lower half of the anther. Anther dorsal, stigma ventral. Rostellum more or less oblong with the apex rounded, yellow. Capsule not seen.
Paratypes Ecuador. Imbabura, Ibarra, El Sagrario, forest near La Carbonería, 3732 m, 0.310255°N, -78.066891°W, 15 May 2017, Tobar, Monge & Obando 2498 (HPUCESI, spirit).
This species was collected in the buffer zone of the Cayambe-Coca National Park on the eastern Imbabura and Pichincha provinces (Fig.
The species has been found in flowers and with fruits at different stages of maturity from May to July, suggesting that reproduction takes place all year round.
The specific epithet honors the Caranqui culture that historically occupied the same areas where this species is distributed.
Lepanthes caranqui is known from two localities within an extent of occurrence of 575 km2. It inhabits both paramo and montane forest where it is more abundant, forming small colonies on tree trunks. Its habitat is not considered to be under pressure since it is located in the buffer zone of a protected area but a potential threat would be the advance of the agricultural frontier. However, it has been observed that this orchid can adapt to moderately disturbed areas and is able to colonize different types of vegetation. Considering the abundant number of mature individuals observed in the field we estimate an approximate number of 500 mature individual and giving that its area of occupancy, habitat quality and the number of mature individuals are not declining we suggest the Least Concern (LC) category following the
Lepanthes caranqui is morphologically most similar to L. pachychila (Fig.
This study was possible thanks to the sponsorship of the Swiss Federal Research Institute (WSL) – National Geographic Society (Grant N° 9952-16) – Swiss National Science Foundation (SNF Grant N° 173342) – European Research Council Advanced Grants (ERC Grant N° 787638) AVES Y CONSERVACION, Secretaría de Gestión Ambiental del Gobierno Autónomo Descentralizado Provincial de El Oro (GADPEO), CODICYT research center of the Pontifical Catholic University of Ecuador Ibarra Headquarters, who managed the necessary funds to carry out the field trips. We also want to thank the Ministry of the Environment of Ecuador for providing permits for specimen collection and transportation that supported our work. [Research Permit HPUCESI N° 05-2015-0343-IC-FAUFLO-DPAI/MAE, Research permit INABIO N° 005-IC-FLO-FAU-DPAEO-MAE research permit Aves y Conservación N° 007-2018-IC-FLO-FAU and mobilization permit HPUCESI: N° MAE-CGZI-DPAI-2016-1643, Aves y Conservación 005-FLO-2019-DPAP-MA, we also want to thank Alexander Hirtz and INABIO for the images used in this document and finally, we want to thank Álvaro Pérez, Gerardo A. Salazar and two anonymous reviewers for their useful suggestions regarding an earlier version of the manuscript.