Amalophyllon miraculum J. L. Clark, 2024
publication ID |
https://doi.org/ 10.3897/phytokeys.242.118069 |
DOI |
https://doi.org/10.5281/zenodo.11583367 |
persistent identifier |
https://treatment.plazi.org/id/48FEC23A-4208-53AD-96F1-C5E2CEEBAB34 |
treatment provided by |
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scientific name |
Amalophyllon miraculum J. L. Clark |
status |
sp. nov. |
Amalophyllon miraculum J. L. Clark View in CoL sp. nov.
Fig. 2 View Figure 2
Type.
Ecuador. Santo Domingo de los Tsáchilas: cantón Santo Domingo, parroquia El Esfuerzo, El Respaldo , 3.5 km east of Segundo Respaldo , finca de Paul Henry , 0 ° 25 ' 25.8 " S, 79 ° 14 ' 7.4 " W, 672 m alt., 19 Mar 2022, J. L. Clark, X. Cornejo, P. Henry & C. Restrepo-Villarroel 16634 (holotype: QCA; isotypes: G, MO, NY, SEL, US) GoogleMaps .
Diagnosis.
Similar to Amalophyllon clarkii , differing in larger and broadly ovate leaves in A. clarkii (> 8 cm long) vs. smaller elongate to lanceolate leaf blades in A. miraculum (<6 cm long); calyx lobes elongate in A. clarkii vs. broadly oblong in A. miraculum ; and abaxial leaf surface green with purple venation in A. clarkii vs. uniformly dark purple in A. miraculum .
Description.
Lithophytic herb with scaly rhizomes; stem short; pendent to horizontal with leaves in a basal rosette. Leaves opposite, subequal; petiole glabrous to sparsely pubescent, 2–5 mm long; blade membranous, fragile when dried, oblong to lanceolate, 1.5–5.0 cm long, 1–2 cm wide, with 6–9 pairs of lateral veins, margins deeply serrate, bright green with dark green venation on adaxial surface, dark purple on abaxial surface, apex acute. Inflorescence reduced to a single axillary flower (without peduncles), usually produced at the apex of leaves or axis of clustered leaves, with 1–3 flowers per axil, inflorescence bracts absent; pedicels slender, curved, 1.5–2.0 cm long; calyx lobes 5, uniformly green, subequal, broadly oblong, nearly free, entire, rounded at apex, ca. 2.0 mm long × 1.0 mm wide; corolla lobes 5, fused at base for 1–2 mm forming a shallow tube, tube light red, lobes uniformly white, lobes entire, subequal, spreading broadly during anthesis, apices rounded, corolla lobes broadly ovate, ca. 2.5 mm long × 2.5 mm wide, glabrous inside and outside; stamens 4, adnate to the base of the corolla tube, filaments yellow, ca. 0.5 mm long, glabrous; nectary absent; ovary nearly superior, subglobose, glabrous, ca. 1 mm long and wide, style ca. 2 mm long, curved, glabrous, stigma capitate. Fruits not observed.
Phenology.
Flowering in March and July. Fruits not observed.
Etymology.
The specific epithet reflects the extraordinary and unexpected persistence of remnant forest patches of an area broadly defined as “ Centinela ” (see next section). Dodson and Gentry (1991) popularized this legendary biodiversity hotspot and brought it to prominence when they reported a mass extinction of plant species from this region. Many of the presumed “ extinct ” species were recently documented, including Gasteranthus extinctus L. E. Skog & L. P. Kvist ( Gesneriaceae ) ( Pitman et al. 2022). Amalophyllon miraculum is sympatric with Gasteranthus extinctus . The presence of several critically endangered species and the recent discovery and description of new species from Centinela represent a miraculous discovery that has shattered a prevailing assumption that the once-thought-lost biodiversity of Centinela had vanished entirely. The heroic efforts of local landowners who maintained small patches of forests (usually surrounding waterfalls) were instrumental in conserving remnant forest fragments. Also crucial are current conservation initiatives by foundations and academic institutions such as the Ecuadorian conservation NGO Fundación de Conservación Jocotoco and the Jardín Botánico Padre Julio Marrero ( JBJM) of the Pontificia Universidad Católica del Ecuador in the nearby city of Santo Domingo.
Distribution and preliminary assessment of conservation status.
Amalophyllon miraculum has been collected in Ecuador’s western Andean slopes in the Santo Domingo de los Tsáchilas province. The only two known subpopulations are in small patches of forest surrounded by large swaths of deforested agricultural landscapes. The forest patch at the Paul Henry farm is approximately 10 hectares and is located in the northernmost part of the Montañas de Ila range in Recinto Milton Murillo. The southern forest patch in the Bosques y Cascadas Las Rocas private reserve is approximately 50 hectares and lies in the intermontane area between the Andean Cordillera and the northern Montañas de Ila (Fig. 1 View Figure 1 ). These patches are approximately 8 km from each other. The current landowners (Paul Henry and Eduardo Díaz C.) are committed to preserving the forest fragments on their property, but broader efforts are urgently needed by governmental and non-governmental agencies to protect these and other nearby forest fragments. The GeoCAT calculated AOO is 8 km 2. Amalophyllon miraculum is preliminarily assessed as Critically Endangered ( CR) based on a limited area of occupancy ( IUCN criterion B 1 where AOO <10 km 2) and the severely fragmented forests ( B 2 a) and ongoing decline of the Centinela forests in western Ecuador ( B 2 bi, ii, iii, iv). Intact forests in the Centinela region are mostly reduced to small (<10 hectares) fragments. Extensive deforestation in western Ecuador, especially Centinela, has resulted in an alarming habitat loss. The area was popularized by E. O. Wilson’s (1992) term as the ‘ Centinelan extinction’ because of initial reports of wide-scale plant extinctions by Dodson and Gentry (1991). One of the presumed extinctions was Gasteranthus extinctus L. E. Skog & L. P. Kvist ( Gesneriaceae ), which was recently documented in more than five forest fragments ( Pitman et al. 2022). The rediscovery resulted in a re-evaluation of its IUCN assessment from Critically Endangered ( CR) to Endangered ( EN). We conducted five field expeditions between 2021 and 2023 and located the only two currently known populations of Amalophyllon miraculum , which is sympatric with the more widespread Gasteranthus extinctus . The only documented populations of Amalophyllon miraculum are inside privately protected areas surrounded by agriculture in unprotected parts of the Santo Domingo de los Tsáchilas province. Effective conservation of this and the other endemic species of the Centinela region will require constant vigilance.
Locating current and future populations of Amalophyllon miraculum is a major challenge because of their small size, ephemeral flowers, and camouflaged foliage on wet moss-covered rock faces. For example, authors Fernández and Zapata recently (April 2024) searched forests in the type locality in Paul Henry’s farm but did not locate extant populations. Likewise, it will require targeted and careful searching to document and locate this elusive species.
Comments.
Most Amalophyllon have leaf margins that are serrate to crenate. Amalophyllon miraculum and A. clarkii (Fig. 2 A View Figure 2 ) are differentiated from other congeners by the presence of deeply serrate to biserrate leaf margins (Figs 2 A View Figure 2 , 3 A View Figure 3 ). The leaf blades of A. clarkii are broadly ovate and nearly 8 cm long (Fig. 2 A View Figure 2 ). In contrast, the leaves of A. miraculum are never more than 6 cm long (Fig. 2 A View Figure 2 ). The calyx lobes in A. clarkii are elongate and narrow (Fig. 3 C View Figure 3 ) vs. broadly oblong in A. miraculum (Fig. 2 C View Figure 2 ). Both Amalophyllon clarkii and A. miraculum share a lithophytic habit but differ in their habitat and posture. Populations of A. clarkii were observed growing erect on a rock in the understory of a shaded forest without direct moisture. Populations of A. miraculum are pendent and have only been observed on wet rocks in streams or where mist is persistent. It was common to locate populations of 10–20 individuals of A. miraculum on wet areas of rock faces and no populations on adjacent dry areas, even when mosses and ferns were shared between the two microhabitats. The rosette-forming individuals of A. miraculum were often pendent. In contrast, populations of A. clarkii are either rosette-forming or with elongate erect shoots, but usually erect. There are always five corolla lobes in Amalophyllon miraculum . In contrast, the number of corolla lobes in A. clarkii is usually five, but occasionally six (Fig. 3 B View Figure 3 ).
Amalophyllon miraculum and A. clarkii are geographically isolated. Amalophyllon miraculum is a narrow endemic from the northern lowlands of the western Andes of Ecuador in the province of Santo Domingo de los Tsáchilas (Fig. 1 View Figure 1 ). Populations of A. clarkii are mainly from the southern lowlands of western Ecuador (Azuay, Guayas, and Los Ríos). One disjunct population of A. clarkii was reported in Boggan et al. (2008) from a unicate collection by Alexander Hirtz from the northern province of Esmeraldas. The collection by Hirtz ( A. Hirtz 3629 - SEL) could not be located or verified and is therefore not included in the distribution map (Fig. 1 View Figure 1 ).
Additional specimen examined.
Ecuador. Santo Domingo de los Tsáchilas: cantón Santo Domingo, parroquia Polanco, sector Bolo Alto, Bosques y Cascadas Las Rocas , propiedad de Eduardo Díaz , near waterfall of the Bolo watershed , 0 ° 28 ' 38.1 " S, 79 ° 11 ' 22.4 " W, 560–600 m alt., 19 Mar 2022, J. L. Clark, L. Hooge, C. Restrepo-Villarroel, R. Clark & E. Muñoz 16805 ( MO, NY, QCA, SEL, US) GoogleMaps .
QCA |
Pontificia Universidad Católica del Ecuador |
G |
Conservatoire et Jardin botaniques de la Ville de Genève |
MO |
Missouri Botanical Garden |
NY |
William and Lynda Steere Herbarium of the New York Botanical Garden |
SEL |
Marie Selby Botanical Gardens |
C |
University of Copenhagen |
CR |
Museo Nacional de Costa Rica |
B |
Botanischer Garten und Botanisches Museum Berlin-Dahlem, Zentraleinrichtung der Freien Universitaet |
E |
Royal Botanic Garden Edinburgh |
O |
Botanical Museum - University of Oslo |
A |
Harvard University - Arnold Arboretum |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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