Lepeostegeres cebuensis Barcelona, Nickrent & Pelser, 2016
publication ID |
https://doi.org/10.11646/phytotaxa.266.1.8 |
DOI |
https://doi.org/10.5281/zenodo.14274146 |
persistent identifier |
https://treatment.plazi.org/id/FF22BC3F-FFF7-FFB7-02AF-F5D3FDBE88B5 |
treatment provided by |
Felipe |
scientific name |
Lepeostegeres cebuensis Barcelona, Nickrent & Pelser |
status |
sp. nov. |
Lepeostegeres cebuensis Barcelona, Nickrent & Pelser View in CoL , sp. nov. — Fig. 1A–H View FIGURE 1
Type: — PHILIPPINES. Cebu Province: Alcoy Municipality, Barangay Nug-as , 17 Dec. 2015, Barcelona 4175 with P.B. Pelser & P. Villarta (holotype: PNH !; isotypes: CAHUP! , CHR! , K! , L! , PUH! , US! ).
Diagnosis: — Lepeostegeres cebuensis is unique among currently known species in the genus by the presence of ridges of brown scales on the leaf and petiole margins and abaxial side of the midvein of young leaves that are decurrent on the young internodes.
Description: —Aerial stem-parasitic shrub, robust, with epicortical runners bearing secondary haustoria. Young internodes slightly angular with two ridges of orange- brown scales. Mature internodes terete or slightly angular, glabrous. Older nodes not or only slightly thickened. Leaves decussate, bifacial; petiole 1.5–3 cm long, adaxially channeled and clasping the terminal bud when young, abaxial surface of midvein and margins with orange-brown scales when young; lamina ovate-elliptic, ca. 5–10 × 2.5–6.5 cm, coriaceous, entirely glabrous when mature, adaxially green and dull, abaxially light green and slightly shiny, base rounded, obtuse or slightly cordate, margin entire, with orange-brown scales when young, apex obtuse to rounded, midvein slightly depressed adaxialy, abaxially prominently raised and with orange-brown scales when young, secondary venation inconspicuous adaxially, faint abaxially. Inflorescences in the axils of the lowermost leaves or ramiflorous, a sessile involucrate head of ca. 25–32 flowers in indistinct sessile triads. Involucre ca. 2.5–4 × 2–2.2 cm, widening towards the apex; involucral bracts 12, decussate, enlarged, chartaceous, not keeled or basal ones slightly keeled when young, imbricate, tightly enclosing the developing flowers, green; upper involucral bracts ovate, ca. 2.5 × 1.5 cm, apex rounded, saccate, glabrous. Bracteoles absent. Pedicel ca. 0.7–0.9 mm long at anthesis, elongating to ca. 2 mm long in fruit. Ovary quadrangular or pentagonal in cross section, ca. 3 × 3 mm, pink, slightly yellow at apex. Calyculus (calyx tube) indistinct, ca. 0.2 mm long, yellowish orange. Corolla in mature bud ca. 4.5–5.2 cm long, 6-merous, regularly gamopetalous, not inflated at base. Corolla in mature, open flower splitting into lobes about half its length with the tube; free petal segments of tube each ca. 18 mm long, pale green; terminal corolla lobes strongly reflexed, ca. 10–12 mm long, red. Stamens with free portion of filaments ca. 2 mm long, pinkish red; anthers basifixed, immobile, not spurred at the base, ca. 7 mm long, apex narrowly tapering, purple when mature. Style simple, very slightly swollen at base, non-articulate above the base, ca. 40–50 mm long, projecting slightly beyond the stamens, ca. 1.0 cm beyond the corolla, pale green, becoming red apically; stigma knob-like, red, darker than apex of style. Fruit depressed orbicular, ca. 5 × 6 mm when immature, slightly angular at base, no stylar base (nipple) present on fruit, calyx limb very short, slightly thickened, scarious, fruit purple when mature; pedicels cup-shaped, irregularly pentagonal (from compression), pale green. Seeds not observed.
Distribution, habitat and ecology: — Lepeostegeres cebuensis is presently only known from Nug-as forest in Alcoy Municipality in southern Cebu. Nug-as forest is a ca. 1000 ha area of fragmented secondary forest over limestone at ca. 300– 900 m.a.s.l. ( Paguntalan & Jakosalem 2007, 2008). It includes regenerating areas of former plantations of exotic trees such as mahogany ( Swietenia macrophylla King in Hooker 1886: pl. 1550; Paguntalan & Jakosalem 2007). This new species grows on various host trees, including Myrsine Linnaeus (1753: 196) sp. , Melicope cf. latifolia ( Candolle 1824: 724) Hartley (1994: 72) , and Rhus taitensis Guillemin (1837: 361) . Handsome sunbird ( Aethopyga bella Tweeddale 1877: 537 ), magnificent sunbird ( Aethopyga magnifica Sharpe 1876: 297 ), red-keeled flowerpecker ( Dicaeum australe Hermann 1783: 223 ), and pygmy flowerpecker ( Dicaeum pygmaeum Kittlitz 1833: 2 ) were observed to feed on floral nectar by one of the authors during previous visits to the area.
Conservation: — Lepeostegeres cebuensis has thus far only been reported from Nug-as forest, which occupies a total area of less than 12 km 2 ( Paguntalan & Jakosalem 2008). This forest does not have protected status, although it is managed by people’s organizations under the Community-based Forest Management Agreement (CBFMA) with the Department of Environment and Natural Resources (DENR; Paguntalan & Jakosalem 2008). Although locally common in the parts of Nug-as forest that were visited by the authors, it is presently unclear if it is present throughout the area and, if so, equally abundant there. It is therefore currently not possible to reliably estimate the number of sites where L. cebuensis occurs or to estimate the total number of individuals in the area. We therefore consider this species to be Data Deficient (DD; IUCN 2014).
Notes: — Lepeostegeres cebuensis most closely resembles L. congestiflorus , but has longer petioles (1.5–3 cm vs. 0.5– 1.5 cm long; Merrill 1909, Danser 1935, Barlow 1997). In addition, the corolla of L. congestiflorus is 2.3–3.2 cm long and greenish-white, greenish yellow, or yellow, and is sometimes red at the base ( Merrill 1909, Danser 1935, Barlow 1997). In contrast, the corolla of L. cebuensis is distinctly larger (4.5–5.2 cm long) and has a pale green tube with red lobes. The involucral bracts of L. congestiflorus were described to be already partially deciduous at anthesis ( Danser 1935), whereas those of L. cebuensis are persistent in early senescent inflorescences. More significantly, however, all currently known Lepeostegeres species are described as entirely glabrous ( Merrill 1909, Danser 1935, Barlow 1997), except for the involucre of the young inflorescences of L. acutiflorus ( Barlow 1997) . In contrast, L. cebuensis has conspicuous orange-brown scales on the leaf and petiole margins and abaxial side of the midvein of the young leaves. Those on the midvein are decurrent on the young internodes, forming two ridges of scales.
Furfuraceous indumentum is seen in a number of species of small-flowered neotropical Loranthaceae ( Kuijt 2011) . The arrangement of this indumentum into stripes on young stems, petioles, midribs, and leaf margins is especially well developed in various species of Oryctanthus Eichler in Martius (1868: 87), a genus of mistletoe found in central and South America: O. asplundii Kuijt (1976: 511) , O. florulentus Urban (1897: 31) , O. guianensis Kuijt (2011: 465) , O. grammatus Kuijt (2011: 463) and O. spicatus Eichler in Martius (1868: 87). At least in Oryctanthus, SEM reveals that the indumentum is composed of corky outgrowths ( Kuijt 2011). Whether the feature in Lepeostegeres cebuensis is developmentally similar remains to be determined. Lepeostegeres (Tribe Elytrantheae , X = 12) and Oryctanthus (Tribe Psittacantheae , X = 8) are phylogenetically distant (Vidal-Russell & Nickrent 2008), hence the furfuraceous lines have likely evolved convergently.
A mistletoe with immature inflorescences was photographed (but not collected) on Mt. Apo in 2012 (PhytoImages DOL74401, DOL74403, DOL7440, DOL74413, DOL74531, DOL108596; Nickrent et al. 2006 onwards). Although this plant keyed to L. congestiflorus , it was not entirely glabrous. Its young stems, petioles, and leaf midveins and margins contained sparsely distributed scales, although not nearly to the extent seen in L. cebuensis . Furthermore, this plant had much shorter petioles and young internodes that were terete instead of slightly angular and ridged. Herbarium specimens of L. congestiflorus examined (Gaerlan, Sagcal, Romero 10919; Gaerlan, Romero, Conran 26525; Reynoso, Garcia, Sagcal 14575; Barbon, et al. 8825, all at BRIT and Jacobs 7004 at MO) did not have these scales, thus it is presently not clear whether this species is polymorphic, if the Mt. Apo mistletoe represents an unknown species, or if it is a hybrid between L. congestiflorus and L. cebuensis . Hybridization and introgression, although generally rare in Loranthaceae , has been proposed for several genera ( Barlow 1997).
PNH |
PNH |
CAHUP |
CAHUP |
CHR |
CHR |
PUH |
PUH |
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