Espeletia Restricta
Espeletia Restricta
Espeletia Restricta
https://www.mapress.com/j/pt/
Article PHYTOTAXA
Copyright © 2020 Magnolia Press ISSN 1179-3163 (online edition)
https://doi.org/10.11646/phytotaxa.433.4.4
Abstract
An intensive exploration of the páramos ecosystem on northwestern Colombia allowed the discovery of a new species
of Espeletia (Millerieae: Asteraceae), E. restricta. Espeletia is an endemic taxon to the páramos of Colombia, Venezuela
and Ecuador, generally found above 3000 m of elevation. Espeletia restricta has a very narrow distribution limited to the
northern Central Cordillera of Los Andes. The new species is similar to Espeletia occidentalis, species occurring in the
Central and Western Cordillera, from which it differs in the size of its synflorescences relative to the rosette length (less than
1.5 times longer than the rosette vs. 2–3 times longer than the rosette) and indument colour (yellowish vs. greenish-white).
The new species was assessed Critically Endangered (CR) due to the small size of its population and the restricted nature of
its occurrence, which makes this taxon of great conservation concern.
Introduction
Espeletia Mutis ex Humboldt & Bonpland (1808: 10) is one of the most emblematic genera occurring in the páramo
ecosystem, and belongs to the tribe Millerieae, subtribe Espeletiinae of the Asteraceae. Espeletia is distributed in the
Andes of Colombia, Ecuador and Venezuela, and occurs at elevations between 2600 and 4600 m (Rauscher 2002).
Diazgranados (2012) estimated the genus to be composed of about 71 species and more than 15 hybrids, although in a
posthumous publication, Cuatrecasas et al. (2013) recognized only 49 species.
Some authors like Cabrera & Ramirez (2014) estimated the rate of endemic species of vascular plants for this
ecosystem at 60%, which is favored by the level of isolation and environmental peculiarities. Páramos are found in
the three Colombian cordilleras, the Sierra Nevada de Santa Marta and the Nudo de los Pastos on the border with
Ecuador (Sarmiento et al. 2013). In the Central Cordillera of Colombia, only five species of Espeletia are found,
this contrasts with 39 species reported by Cuatrecasas et al. (2013) for the Eastern Cordillera, which is attributed by
Cuatrecasas (1986) to the environmental homogeneity of the Central Cordillera during the Holocene: E. hartwegiana
Schultz Bipontius ex Cuatrecasas (1933: 17) has a very wide distribution in the Central Cordillera of Colombia, from
the border with Ecuador to the Nevado del Ruiz in the north-central part of the cordillera; E. schultesiana Cuatrecasas
(1942: 26) and E. pycnophylla Cuatrecasas (1942: 24) are found in the southern part, in the departments of Nariño
and Putumayo, while E. idroboi Cuatrecasas (1977:12) occurs in The Papas páramo, in the departments of Cauca and
Huila, and E. occidentalis Smith (1935: 520) represents the northern species for this cordillera, in the department of
Antioquia (Cuatrecasas et al. 2013).
The Andes in Colombia reach the altitude of 5775 m and are divided into three Cordilleras named Western,
Central and Eastern. The Western and Central Cordilleras reach north-western South America including the department
of Antioquia, where they disappear. Antioquia, located in northwestern Colombia, has six páramo complexes in the
Central and Western Cordilleras of the Colombian Andes (Sarmiento et al. 2013, Alzate & Murillo 2016) totalling
46.000 ha, of which the páramo of Sonson has an extension close to 3,400 ha.
According to Alzate et al. (2016), the páramo of Sonsón is located in the southeastern part of the Department of
Antioquia, isolated by the tropical rainforest ecosystem, reaching an elevation of 3.340 m and developing very steep
The morphological study was based on specimens of Espeletia collected in the department of Antioquia and specimens
available in COL, HUA, MO, NY and US (herbarium acronyms follow Thiers 2019) and images available at JSTOR
(2018). General morphological characterization and description were made using the terminology from Cuatrecasas
et al. (2013).
For descriptions of capitula, ray and disc florets, phyllaries and achenes, fresh mature capitula were first fixated in
a formal-acetic-alcohol solution and then preserved in an ethanol-glycerol solution. For leaf architecture descriptions,
dry leaves were cleared in a sodium hydroxide solution, and then stained with safranin dye, based on the protocol
proposed by Vasco et al. (2014). Descriptions were made following the terminology established by Ellis et al. (2009).
Indument descriptions were made following the terminology proposed by Beentje (2010). Threat level of the species
was assessed using the Geospatial Conservation Assessment Tool (GeoCAT) (Bachman et al. 2011).
A key to Espeletia species from the northern Central and Western Andes of Colombia is provided in this work.
Taxonomy
Type:—COLOMBIA. Antioquia: Municipio Sonsón, Vereda La Paloma, páramo de Sonsón, Cerro de Las Palomas, 3370 m a.s.l., 5°43’34”
N, 75°14’58” W, 7 January 2016 (fl), F. Alzate 5220 (holotype: HUA! [2 sheets]; isotypes: MO!, COL!).
Espeletia restricta is a herb with a stem up to 1.2 m tall, yellowish indument (grayish in E. occidentalis), laminae
24–40 × 6–12 cm; synflorescences 23–50 cm long, 0.8–1.2(–1.5) times longer than the rosettes, bracts very variable in
number and phyllotaxy; ray florets 31–42, disc florets 110–153.
Caulirosulous herbs with a stem usually not exceeding 0.6 m tall but on occasions up to 1.2 m, not ramified, erect,
densely covered by marcescent leaves; stem diameter at rosette base 5–12 cm. Rosette 0.30–0.42 m tall and 0.32–0.53
m in diameter, appearance yellowish. Leaves 29–43 cm long, alternate, simple, sessile. Laminae 24–40 cm × 6–12
cm, elliptic to oblong, symmetrical, gradually narrowing toward base, base truncate and obtuse, width at lamina base
(0.7–)1.4(–3) cm, apex acute, apex shape usually straight but sometimes slightly acuminate, margins entire and slightly
revolute. Blades coriaceous, flexible in all stages of development, adaxially rugulate, venular reticulum conspicuous,
depressed; abaxially the midvein prominent, longitudinally striated, secondary nerves 6–15 mm apart, noticeably
prominent, excurrently attached to the costa, regularly spaced in the center of the laminae and frequently becoming
closer toward base and apex, deviation angle slightly uniform or increasing upwards, varying between 17°–44°,
brochidodromous, occasionally weakly anastomosed with each other near the margin, intersecondary veins strongly
developed when present, usually one per intercostal area, longer than the half of subjacent-secondary longitude, course
proximally and distally parallel to main secondaries, tertiary nerves irregularly reticulated, forming a raised, tiny
network with quaternary and quinary nerves, both of which are regularly polygonal reticulated; epimedial tertiaries
reticulated and exterior tertiaries course variable, often ending at the margin. Areolation well developed, areoles of
relatively consistent size and shape, minutely pilose on the inside. Marginal ultimate venation looped. Freely ending
veinlets not visible. Sheaths 2.7–5.9 cm × 2.0–4.1 cm, multinerved, ovate, apex obtuse, adaxially glabrous, green-
brown, abaxially the indument dense. Synflorescences thyrsoid, usually 3–4(–7) coetaneous, 23–50 cm long, 0.8–1.2(–
1.5) times longer than the rosettes. Synflorescence’s main axe 5–13 mm in diameter above base, erect, basally rigid,
distally flexible; proximal part 0.39–0.87 of total length, with a very variable number (0–8) and phyllotaxy of bracts,
those being sometimes 1–3 pairs decussate, other times being 1 opposite basal pair followed by 1–6 alternate bracts or
2 basal decussate pairs followed by 1–4 alternate bracts, even in some cases all the bracts alternate and occasionally
a new species of Espeletia (ASTERACEAE) Phytotaxa 433 (4) © 2020 Magnolia Press • 289
without bracts. Bracts, when present, 15–23.3 cm × 2.1–4.5 cm, oblong attenuate towards the base, with somewhat
connate sheaths, apex acute, the lowermost ones at 0–8 cm above the base of the synflorescence, the following ones
gradually decreasing upwards. Distal part of the synflorescence with 4–14 capitula, the most distal branch usually
with 3 but sometimes with 1–2 capitula. Indument on axes and branches yellowish, dense, lanate, longer and less
entangled in main axes, bracts with indument similar to leaves. Capitula 20–27 mm in diameter, radiate, usually erect,
involucre subglobose, each capitulum with 143–186 flowers; ligular circle 25–33 mm in diameter and disc 15–20 mm
in diameter. Phyllaries becoming smaller inwards and giving the appearance of being distributed in 2–3 whorls, but
actually spirally arranged; the external sterile ones usually 4–5, coriaceous, a basal opposite pair of them differentiated
for being longer, triangular and with a markedly acuminate apex, meanwhile the remaining ones have acute or slightly
rounded apex; the internal fertile ones 3–10, chartaceous, discontinuous, apex acute to rounded. Receptacles convex,
glabrous, paleate. Ray florets 31–42; corollas true ray, yellow; tubes 1.2–2.0 mm long, densely pilose; limbs 7.2–9.9 ×
2.5–3.6 mm, oblong to elliptic, apically 2–3-lobed, 7–10-veined. Style 4.5–5.9 mm long, stigmatic branches 2.5–4.6
mm long. Achenes 3.7–4.2 mm × 1.6–2.8 mm, obconic, triangular in transversal section, usually 3(–6)-ribbed, dark
brown when mature. Pappus absent. Disc florets 110–153; corollas tubular yellow, throats 5–5.3 mm long, mostly
glabrous, lobes 5, triangular, tubes 2.1–2.7 mm long. Anthers 2.8–3.9 mm long, apical appendage about 1/8 of anther
lengths, rounded. Style 8–9 mm long, stigmatic branches 0.4–0.5 mm long, broadening distally, papillose; rudimentary
ovary present. Pappus absent. Paleae 7.0–8.7 × 2.5–3.3 mm, elliptic, scarious, rigid, basally enclosing florets, usually
7-veined with veins occasionally ramifying dicotomically at medial-distal section, apex acute.
Indument description:—Leaves with indument thickly and densely lanate throughout, adaxially yellowish,
forming a uniform cover, with the long trichomes straight to undulated, appressed and not so entangled. The costa
abaxially sericeous, yellowish, the rest of the lamina with whitish and entangled trichomes. Sheaths abaxially with
a dense indument, trichomes long, barbate, undulated, ascending, whitish. Ray florets densely pilose, trichomes
glandular, multicellular, ascending or patent. Disc florets with few external minute trichomes in the tube portion.
Paleae pubescent apically, on edges and abaxially, mostly over veins, glabrous adaxially.
Etymology:—The name refers to the extreme level of endemism in the distribution of this taxon.
Morphological affinities:—Espeletia restricta is similar to Espeletia occidentalis subsp. antioquiensis
(Cuatrecasas 1942: 24) Cuatrecasas (2013: 216) because both have a short stem, no more than 1.5 m, similar number
of capitula per synflorescence (4–14) and distributed in the north of the Central Cordillera. Espeletia restricta differs
by the size of its synflorescences relative to the rosette length (less than 1.5 times longer than the rosette vs. 2–3 times
longer than the rosette), indument colour (yellowish vs. greenish-white) and synflorescences total length (< 50 cm vs.
> 60 cm).
Taxonomic affinities:—Cuatrecasas et al. (2013) proposed a taxonomical affinity for the Espeletia species
occurring in the Western Cordillera of Colombia. These authors suggested that E. frontinoensis Cuatrecasas (1977:
15) is sister to E. praefrontina Cuatrecasas (1980: 10), both species endemic of the Western Cordillera. The last two
species form a clade that also would include E. hartwegiana and E. pycnophylla, species with a wider distribution. As a
basal group to this clade, Cuatrecasas et al. (2013) proposed E. occidentalis subsp. antioquensis. In the same work, the
authors suggested that E. occidentalis subsp. antioquensis is related to E. grandiflora Humboldt & Bonpland (1808:
11) which occurs at the Eastern Cordillera. Espeletia restricta is distributed at the same Cordillera as E. occidentalis
and both have the morphological traits that suggest their taxonomic affinity.
Distribution, habitat and ecology:—The new species have been collected only in two areas of the páramo of
Sonsón, Department of Antioquia in the northern Andes Cordillera. Although the total area of the páramo is 8707 ha,
E. restricta only grows in an area of approximately 2 ha, at elevations between 3300 and 3363 m a.s.l. The habitat of
E. rectricta has a vegetation characterized by a very dense and diverse páramo flora, dominated by representatives of
Asteraceae, Bromeliaceae and Poaceae families. The dominant vegetation corresponds to shrublands with abundant
small plants of the genera Cortaderia, Guzmania, Paepalanthus and Disterigma.
The Sonsón páramo complex is located in the Central Cordillera of Colombia, southern department of Antioquia
and northern department of Caldas (Alzate et al. 2016). The mountain topography of this region allows to have scarce
páramo zones, most of the time isolated from one another (Alzate et al. 2016).
Espeletia restricta populations are found in the southern part of the Central Cordillera of Department of Antioquia,
while other species of Espeletia growing in the nearest area of this Cordillera are separated by a depression formed
due to Porce river canyon.
Conservation status:—This new species has a very restricted distribution and the populations have a low number
of individuals, which makes it very susceptible to any environmental change, such as those generated by climate
290 • Phytotaxa 433 (4) © 2020 Magnolia Press ALZATE & GIRALDO
change and anthropic activities. Considering these conditions, it is evident that E. restricta is under a very high risk
of extinction, since the possible area of occupation of the species would be reduced in a scenario of global warming.
Using the occurrence data and based on the assessment carried out on GeoCat, the species was found Critically
Endangered (CR) for both IUCN metrics, the extent of occurrence (EOO) and the area of occupancy (AOO).
Additional specimens examined:—COLOMBIA. Antioquia: Municipio Sonsón, Vereda La Paloma, páramo
de Sonsón, Cerro de Las Palomas, 3370 m.a.s.l, 5°43’34” N, 75°14’58” W, 7 October 2011 (fr), F. Alzate, O. Díaz, S.
Varela, P. Pérez & S. Murillo 4234 (HUA); Municipio Sonsón, Vereda San Francisco, páramo de Sonsón, Cerro de
Las Palomas, alrededores de la escuela para subir a la cima del cerro, 3250 m.a.s.l, 5°43’32” N, 75°15’00” W, 16 June
2012 (fl), O. Díaz, S. Varela, P. Pérez & M. Hincapié 861 (HUA); Municipio Sonsón, Vereda La Paloma, páramo de
Sonsón, Cerro de Las Palomas, 3370 m.a.s.l, 5°43’34” N, 75°14’58” W, 16 October 2009 (fr), F. Alzate, A. Álvarez,
J.P. Naranjo, J. Marín, N. Montaño, S. López, A. Diez, S. Monsalve, W. Berti, S. Villa & E. Ospina 3337 (HUA).
Key to the species of Espeletia occurring in the northern region of Central and Western Cordilleras of Colombia,
corresponding to the department of Antioquia
1. Synflorescences > 60 cm long, 2–3 times longer than the rosettes...........................................................E. occidentalis
- Synflorescences < 50 cm long, up to 1.5 times longer than the rosettes.............................................................................................2
2. Lamina width > 6 cm, subtending bracts normally surpassing peduncles, anthers more than 2.8 mm long; Central Cordillera.........
.............................................................................................................................................................................................E. restricta
- Lamina width < 5.6 cm, subtending bracts normally shorter than peduncles, anthers less than 2.5 mm long; Western Cordillera.....
.............................................................................................................................................................................................................3
3. Proximal part of synflorescences with 1–2 pairs of bracts........................................................................................... E. praefrontina
- Proximal part of synflorescences aphyllous................................................................................................................ E. frontinoensis
FIGURE 1. Espeletia restricta. A. Habitat. B. Habit. C. Capitulum, frontal view. Photos by S. Giraldo.
a new species of Espeletia (ASTERACEAE) Phytotaxa 433 (4) © 2020 Magnolia Press • 291
FIGURE 2. Espeletia restricta. A. Adaxial view of leaf. B. Synflorescence. C. Outer phyllary (abaxial view). D. Outer phyllary (adaxial
view). E. Inner phyllary (abaxial view). F. Inner phyllary (adaxial view). G. Ray floret with immature achene. H. Disc floret. I. Palea
(adaxial view). J. Achene (dorsal view). Illustrations made by Adriana Sanín (HUA).
292 • Phytotaxa 433 (4) © 2020 Magnolia Press ALZATE & GIRALDO
Acknowledgments
We thank members of HUA for providing material for the description as well as for facilitating botanical collections
and Adriana Sanín (HUA) for preparing the illustrations. We also thank Herber Sarrazola for useful comments on the
manuscript.
References
Alzate-Guarín, F. & Murillo-Serna, J.S. (2016) Angiosperm flora on the páramos of northwestern Colombia: diversity and affinities.
PhytoKeys 70: 41–52.
https://doi.org/10.3897/phytokeys.70.8609
Alzate, F., Jiménez, J. & Sarrazola, H. (2016) Sonsón, un nuevo complejo de páramos en Colombia. In: Quijano, M. (Ed.) Flora del
Oriente Antioqueño. Biodiversidad, Ecología y Estrategias de Conservación. Academia Colombiana de Ciencias Exactas, Físicas y
Naturales. Colección Jorge Álvarez Lleras Número 30, Bogotá, pp. 19–42.
Bachman, S., Moat, J., Hill, A.W., de la Torre, J. & Scott, B. (2011) Supporting Red List threat assessments with GeoCAT: geospatial
conservation assessment tool. (Version BETA). In: Smith, V. & Penev, L. (Eds.) e-Infrastructures for data publishing in biodiversity
science. ZooKeys 150: 117–126.
https://doi.org/10.3897/zookeys.150.2109
Beentje, H.J. (2010) The Kew plant glossary: an illustrated dictionary of plant terms. Royal Botanic Gardens, London, 164 pp.
Cabrera, M. & Ramirez, W. (2014) Restauración ecológica de los páramos de Colombia. Transformación y herramientas para su
conservación. Instituto de Investigación de Recursos Biológicos Alexander von Humboldt (IAvH), Bogotá, 296 pp.
Cuatrecasas, J. (1933) Plantae Colombianae Novae. Trabajos del Museo Nacional de Ciencias Naturales, Serie Botánica 26: 1–30.
Cuatrecasas, J. (1942) Notas a la flora de Colombia, V. Revista de la Academia Colombiana de Ciencias Exactas, Físicas y Naturales 5
(17): 16–39.
Cuatrecasas, J. (1976) A new subtribe in the Heliantheae (Compositae): Espeletiinae. Phytologia 35: 43–61.
https://doi.org/10.5962/bhl.part.2608
Cuatrecasas, J. (1977) Miscellaneous notes on neotropical flora, IX. Phytologia 38: 7–22.
https://doi.org/10.5962/bhl.part.23374
Cuatrecasas, J. (1980) Miscellaneous notes on neotropical flora, XII. Phytologia 47: 1–13.
https://doi.org/10.5962/bhl.part.4450
Cuatrecasas, J. (1986) Speciation and Radiation of the Espeletiinae in the Andes. In: Vuilleumier, F. & Monasterio, M. (Eds.) High Altitude
Tropical Biogeography. Oxford University Press, New York, pp. 267–303.
Cuatrecasas, J., Robinson, H.E. & Wagner, W.L. (2013) A systematic study of the subtribe Espeletiinae (Heliantheae, Asteraceae). The
New York Botanical Garden Press, New York, 689 pp.
Diazgranados, M. (2012) A nomenclator for the frailejones (Espeletiinae Cuatrec., Asteraceae). PhytoKeys 16: 1–52.
https://doi.org/10.3897/phytokeys.16.3186
Diazgranados, M. & Barber, J.C. (2017) Geography shapes the phylogeny of frailejones (Espeletiinae Cuatrec., Asteraceae): a remarkable
example of recent rapid radiation in sky islands. PeerJ 5: e2968.
https://doi.org/10.7717/peerj.2968
Ellis, B., Daly, D.C., Hickey, L.J., Johnson, K.R., Mitchell, J.D., Wilf, P. & Wing, S.L. (2009) Manual of leaf architecture. Cornell
University Press, New York, 190 pp.
Humboldt, F.W.H.L. & Bonpland, A.J.A. (1808) Plantae Aequinoctiales 2 (9). De l’imprimerie de J. Smith, Paris, 191 pp.
JSTOR (2018) Global Plants. Available from: https://plants.jstor.org/ (accessed: 10 September 2018).
Lüttge, U. (2007) Physiological ecology of tropical plants. Springer Science & Business Media, Berlin, 458 pp.
Rauscher, J.T. (2002) Molecular phylogenetics of the Espeletia complex (Asteraceae): evidence from nrDNA ITS sequences on the closest
relatives of an Andean adaptive radiation. American Journal of Botany 89: 1074–1084.
https://doi.org/10.3732/ajb.89.7.1074
Sarmiento, C., Cadena, C., Sarmiento, M., Zapata, J. & León, O. (2013) Aportes a la conservación estratégica de los páramos de Colombia:
Actualización de la cartografía de los complejos de páramo a escala 1:100.000. Instituto de Investigación de Recursos Biológicos
Alexander von Humboldt, Bogotá, 88 pp.
Sklenář, P., Luteyn, J.L., Ulloa Ulloa, C., Jorgensen, P.M. & Dillon, M.O. (2005) Flora genérica de los páramos: Guía ilustrada de las
plantas vasculares (Memoirs of The New York Botanical Garden 92). The New York Botanical Garden Press, New York, 499 pp.
a new species of Espeletia (ASTERACEAE) Phytotaxa 433 (4) © 2020 Magnolia Press • 293
https://doi.org/10.1086/523148
Smith, A.C. (1935) The genus Espeletia: A study in phylogenetic taxonomy. Brittonia 1: 479–530.
https://doi.org/10.2307/2804673
Thiers, B. (2019) Index Herbariorum: A global directory of public herbaria and associated staff. New York Botanical Garden’s Virtual
Herbarium. Available from: http://sweetgum.nybg.org/science/ih/ (accessed 24 January 2019)
Vasco, A., Thadeo, M., Conover, M. & Daly, D.C. (2014) Preparation of samples for leaf architecture studies, a method for mounting
cleared leaves. Applications in plant sciences 2 (9): 1400038.
https://doi.org/10.3732/apps.1400038
294 • Phytotaxa 433 (4) © 2020 Magnolia Press ALZATE & GIRALDO