A new species of Phalaenopsis Orchid (Orchidaceae: Vandeae, Aeridinae)
has been discovered, based on study by Destario Metusala and Peter O’Byrne. The
orchid was obtained from Kapuas Hulu, West Kalimantan Province, Indonesia.
Description of morphological data is based on observations on living plants, wet
preserved material, herbarium specimens, and color photographs from cultivated individu.
Comparison of morphology with other related Phalaenopsis species (P.
gigantea, P. doweryensis, and P. rundumensis) are carried out based on data
from protologists, living plants, specimens herbarium and photographs. The
results of the study indicate that there are significant differences in the
morphological character of the flower, so the Phalaenopsis sp specimens from
Kapuas Hulu are described as new species with name of Phalaenopsis kapuasensis
Metusala & P.O'Byrne.
Phalaenopsis kapuasensis Metusala & P.O'Byrne belongs in the same
complex as P. gigantea J.J.Sm., P. doweryensis Garay & Christenson, and P.
rundumensis P.J. Cribb & A. Lamb. All these species are endemic to Borneo.
Phalaenopsis kapuasensis. Photo by Muhammad Gunawan
Phalaenopsis gigantea was described in 1909 from specimens collected on
the 1896-1897 Nieuwenhuis trans-Borneo expedition, and cultivated at Bogor
(Smith, 1909). It has been recorded from Kalimantan, Sabah and Sarawak in lowland
dipterocarp forest, hill dipterocarp forest and mossy hill forest from sea
level to 900 m. Flower colour is somewhat variable, and two colour forms have
been formally described. Although the species is well-known in cultivation, the
majority of specimens are ex-nursery, and there are surprisingly few documented
records of wild-collected plants. Consequently, details of range, habitat and
infra-specific variation of the wild population are poorly understood.
Phalaenopsis doweryensis was described in 2001 from plants cultivated
in the USA that reportedly originated in Sabah (Christenson, 2001). The
researcher have seen all the material originated in nurseries; the range,
habitat and infraspecific variation of the wild population are unknown. On-line
photographs show some variation in flower colour, especially the colour and
amount of spots/streaks on the tepals. One or two of these photos appear to show
P. kapuasensis rather than P. doweryensis. Phalaenopsis rundumensis was described
in 2011 from plants collected at 600-800 m in hill forest in the Rundum area of
Sabah, and cultivated at Tenom Orchid Centre (Cribb & Lamb, 2012).
Illustrations in the protologue show considerable variation in flower
colour. Although the species is not yet widely cultivated, the few online
photographs also show considerable variation in flower colour. The extent of
range and habitat of this species are uncertain, and the infraspecific morphological
variation is
unknown. In their protologue, Cribb & Lamb implied that P.
rundumensis may be intermediate between P. gigantea and P. doweryensis, and
stated that the exact relationship of P. rundumensis to P. gigantea needs
further investigation.
Kipandi Park in Sabah has two Phalaenopsis specimens that were purchased
from a local orchid hunter, who collected them from a single locality. Both have
the habit and tepal shape of P. rundumensis. Both have an inflorescence that
elongates slowly, producing 2-3 flowers at a time, which is a characteristic of
P. rundumensis. The 5.8 cm high flowers on one plant have an elliptic lip midlobe
with the lateral margins in the middle slightly erose, and towards the apex somewhat
expanded and dentate; this is typical of P. rundumensis. The other has smaller
flowers (4.8 cm high) with an obovate midlobe that has lateral margins towards
the apex considerably expanded and deeply dentate, which is closer to P. doweryensis
than P. rundumensis.
The Researcher are still far from understanding the taxa in this
complex. Unfortunately, most newly-collected specimens are sold to nurseries or
private individuals rather than being donated to botanic gardens or placed in
herbaria, so the information needed to resolve the complex is being lost to
science.
Although we are reluctant to add to the confusion surrounding this complex,
the presence of a distinct taxon needs documenting. Since P. kapuasensis is as
distinct from the other species as they are from each other, we have opted to describe
it as a species rather assign it subspecific status under one of the other taxa.
In 2011, the first first researcher saw a picture of a strange
wild-collected Phalaenopsis labeled as Phalaenopsis gigantea ‘yellow’ from West
Kalimantan, and asked the owner of the plant, Muhammad Gunawan, to send some
flowers for examination. Muhammad Gunawan kindly supplied some flowers (as
spirit material) in mid 2011. The first author initially thought this material
represented a form of Phalaenopsis gigantea with narrower tepals, a presumption
that was supported by the lip midlobe shape, which is quite similar to that of
P. gigantea.
The status of this plant remained unclear until some plants were
offered for sale in a local
exhibition held in Jakarta in 2017. In mid 2017, Dr. Ingrid Hilman, one
of the orchid hobbyists who has the plant, kindly gave the first author some
fresh flowers, and the researchers were able to re-examine its status.
Below are the description of Phalaenopsis kapuasensis
Type:—INDONESIA. Borneo, West Kalimantan Province, Kapuas Hulu
Regency, RIO 9005 (holotype: BO!).
Diagnosis:—Phalaenopsis kapuasensis is close to Phalaenopsis
rundumensis but differs in having shorter tepals not more than 17 mm long, a
lip with a hairy midlobe and different shape sidelobes. Pendent epiphytic herb.
Roots cylindrical to slightly flattened when creeping, greensilvery, textured
on surface. Stem 4-5 cm long.
Leaves usually 3-6 per stem, pendent, oblong to oblong-elliptic, 22-48
× 5-10 cm, succulent, thick, waxy, obtuse to unequally retuse, green;, not
compressed, green.
Inflorescences several, pendulous, 10-34 cm long, peduncle c. 0.3 diam,
glabrous; rachis somewhat thicker than the peduncle, up to 19 cm long × 0.5 cm
diam, occasionally with 1-2 short branches from
below the rachis, light green to dark green, bearing up to 30 flowers
(or more) with 2- 10 open simultaneously; floral bract triangular, 2.5-3.0 ×
3.0 mm, acute, green.
Flower 2.6-3.0 cm across, rather flat and somewhat stellate; sepals and
petals greenish-yellow to pale-yellow with continuous or discontinuous brown or
maroon-red transverse bars; lip white, midlobe with longitudinal purple lines
on upper surface, stained pink below, sidelobe interior often suffused, spotted
or streaked purple, basal swelling yellow or gold; column and anther-cap white
to cream.
Pedicel-with-ovary c. 1.5 cm, green. Dorsal sepal elliptic, 14-16 ×
6.5-10.0 mm, apex obtuse to acute. Lateral sepals obliquely elliptic-ovate to
elliptic, 15-16 × 8-11 mm, apex obtuse to acute, often slightly acuminate.
Petals elliptic to oblanceolate, 14-16 × 6-10 mm, obtuse to acute. Lip porrect,
3-lobed, 11-12 mm, fleshy; side lobes erect, oblong-falcate, 5-6 × 2.5-3.0 mm,
with an oblong triangular fleshy thickening along front margin, apex truncate
with a small notch in distal half of upper margin; mid-lobe shallowly concave,
obovate or elliptic, 7-8 × 4-7 mm, margins erose, adaxial surface distally with
covering of short, rather broad hairs, with a low median keel extending from
base that elevates in distal third of midlobe to become an erect fleshy median
crest that extends beyond midlobe apex; two thin
plate-like keels with erose margins extend longitudinally on each side
of median keel; between sidelobes a callus forms two forward-projecting
tapering horns that slightly outcurve at their tips, below and in
front a thinner oblong-ovate plate extends onto midlobe, bifid at tip;
blade
apex obtuse to acute.
Column porrect, slightly decurved near the apex, 7.0-7.5 mm, from a
narrow base broadening to 3.5 mm before apex, shortly pubescent on ventral
surface; anther cap sub-globose with two triangular plate-like projections on
the front, 2.5 x 3 mm, apex obtuse; pollinia 2 with a cleft, sub-globose, 1.5 x
1 mm; stipe 2 mm, narrow and curved.
Distribution: Indonesia, West Kalimantan (exact locality withheld for
conservation reasons).
Habitat and ecology: Lowland forest; 50- 200 m.
Etymology: Named after Kapuas Hulu Regency, the area where the type
material originated.
Phenology: January, May, July, August, September.
Cultivation: grown by attaching the plant on a wood slab with some moss
filling in the root area. Plant should be hung in a place with good air
circulation, light intensity 50-70 %, and watered regularly,
especially the root area.
The best character for differentiating Phalaenopsis kapuasensis from
other taxa in this complex is the presence of short, rather thick hairs on the
upper surface of the lip midlobe. Phalaenopsis kapuasensis can be distinguished from P. gigantea by the narrower leaves (up to 10
cm) with an obtuse to retuse apex, an inflorescence with flowers produced
sequentially, and smaller flowers (26-30 mm wide) with
narrower tepals.
Phalaenopsis gigantea has broader leaves (up to 25 cm) with a broadly
rounded apex, and the
inflorescence has all the flowers open at the same time. Phalaenopsis
gigantea has larger (45-50 mm wide) flowers with relatively broader tepals that
usually overlap. In P. gigantea the midlobe shape is too variable to use in
diagnosis, but it never has hairs on the upper surface.
Phalaenopsis kapuasensis, P. doweryensis and P. rundumensis are similar
in plant habit, except that the
former has up to six leaves per stem; the latter two usually have two
or three leaves which are relatively shorter and broader (to 20-23 × 7-10 cm).
All three species flower sequentially, and have one to several
flowers open at a time. Phalaenopsis kapuasensis has flowers of similar
size to P. doweryensis, but differs in having a midlobe without extension on
the upper lateral margins.
Phalaenopsis doweryensis has a midlobe with the lateral margins at the
front extended into conspicuous minutely lacerate-dentate hooks, and it lacks
hairs on the upper surface. Phalaenopsis kapuasensis differs from P. rundumensis
in having smaller flowers (26-30 mm wide) with oblong sidelobes that are
distinctly notched on the rather broad upper margin and a midlobe that is hairy
on the upper surface. By contrast, P. rundumensis has larger flowers (45-50 mm),
the sidelobes are triangular with a narrow entire upper margin, and the midlobe
is hairless with slightly papillose lateral margins.
Since the midlobe shape is variable in P. kapuasensis and P. gigantea,
and the variation is unknown in P. rundumensis (see Introduction), that
character should not be used as a diagnostic character for species in this
complex.
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