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Rediscovery of an outstanding Nepenthes: N.
aristolochioides (Nepenthaceae)
Dr. Joachim Nerz
Keywords: observations: Nepenthes aristolochioides, Nepenthes talangensis
Summary
The morphology and ecology of a recently described Nepenthes-species,
Nepenthes aristolochioides (Jebb & Cheek, 1997) from Central-Sumatra,
is described and illustrated in this article.
Introduction
During a visit to the Herbarium of Leiden in 1988 I became
aware of a rather poor herbarium specimen of a Nepenthes from Central
Sumatra marked "new species?" It was collected in 1956 by Prof.
Willem Meijer, a well-known Rafflesia-specialist. The species seems
to be closely related to Nepenthes talangensis. In summer of 1996,
Dr. Jan Schlauer organized a meeting with Prof. Meijer in the Palmengarten
Frankfurt, Germany. At this meeting, he showed us a photo of the mentioned
new Nepenthes species with extraordinary new features. The new
features of it will be discussed later on in this article. To get more
detailed information about it, in June of 1996 Katrin Hinderhofer and
I organized a field rip to Sumatra, where we were able to rediscover this
species in its natural habitat (Back Cover). The species has been described
recently (Jebb & Cheek 1997) as Nepenthes aristolochiodes.
Because of the new details which we obtained, I will now give a detailed
description of the examined material.
Plants usually climbing. climbing stems reaching up to
5-8 m height, the part with adult leaves 3-5 mm thick, cylindrical to
obtusely angular, internodes 7-10 cm long, leaves of the rosettes and
climbing stems thick, coriaceous, sessile, lanceolate-spathulate, about
8-14 cm long, up to 3 cm broad, apically acute or obtuse, attenuate towards
the base, leaves clasping the stem, not decurrent. Pinnate nerves irregularly
reticulate, longitudinal ones 3-5 on each side, originating from the leaf
base, running parallel in the outer 2/3 of the lamina. Pitchers of the
rosettes (Figure 1) originating with a short curve, 3-5 mm wide from the
hanging end of the tendril. Tendrils about twice as long as the leaves,
without curl. Pitchers utriculate, thick, coriaceous, 5-7 cm high, 2.5-3
cm wide, with two fringed wings, the wings up to 1 mm broad, the fringe
segments up to 3-5 mm long, 0.5 to 2 mm apart; mouth orbicular to ovate,
up to 1.5 cm wide, oblique to vertical, facing forward. Peristome flattened,
7-20 mm wide, the ribs 1/2 -1/3 mm apart, the teeth of the inner margin
2-3 times as long as broad. Inner side of the pitcher wholly glandular.
In the lower half of the pitcher overarched glands, 0.2-0.3 mm in diameter,
200 cm-2, smaller ones, 500 cm-2 in the upper part
of the pitcher. Lid orbicular to ovate, 1-1.5 cm in diameter, in front
of the pitcher. Lower surface without appendage, with rather large glands
at the whole surface, especially near the midrib. Three prominent nerves
on each side of the midrib. Spur broad and flattened, 3-7 mm long, branched,
inserted close to the lid. Pitchers of the climbing stem (Figure 2) originating
with a short curve, 10 mm wide from the hanging end of the tendril, narrow
infundibuliform, 7-10 cm high, 2.5-4 cm wide, with 2 prominent ribs; mouth
almost to completely vertical, facing forward. Peristome flattened, 4-6
mm wide, the ribs 1/3 mm apart, the teeth of the inner margin 2-3 times
as long as broad, not distinct. Interior surface of the pitcher wholly
glandular. In the lower part of the pitcher slightly overarched glands,
0.3-0.4 mm in diameter 200 cm-2, smaller overarched glands
in the upper part, 250 cm-2, 0.2-0.3 mm in diameter. Lid ovate,
in front of the pitcher. Lower surface without appendage, with rather
large glands over the whole surface. Three to four prominent ribs on each
side of the midrib. Spur broad and flattened, 3-5 mm long, branched, inserted
close to the lid. Female inflorescence a raceme, the peduncle 4-5 cm long,
2-4 mm thick, the axis 14-15 cm long. The pedicels all of them 1 flowered,
the lower ones 12 mm, the upper ones 6 mm long. Fruits 15-20 mm long,
the valves lanceolate, 3 to 4 mm broad, gradually attenuate towards both
ends. Seeds filiform. Colour of herbarium specimens: Brown to dark brown,
pitchers with dark spots. Colour of living specimens: Vegetative parts
light green, leaves with white hairs at the margins, pitchers ivory white
to reddish with numerous red spots. Rim usually red to dark red, especially
in rosette-pitchers. Lid on the lower surface red, on the upper surface
yellowish with small red spots.
Distribution and Ecology
This species is only known from a very limited area in
central Sumatra, where it grows at an altitude of 2400 m. It grows in
mossy forest, climbing in shrubs and small trees. The typical mossy forest
with Sphagnum on the ground was restricted just to the very top
of the explored ridge. Just here some few single plants of Nepenthes
aristolochioides were found, mostly climbing--only very few rosette-plants
were growing in the moss. A gracile type of Nepenthes singalana
is growing together with Nepenthes aristolochioides, usually in
Sphagnum, sometimes climbing up into the shrubs and treelets.
Other Nepenthes Species of This Mountain:
At an altitude of about 1800-2100 m in montane forests
and in Pandanus-swamps on the shoreline of a crater lake, Nepenthes
gymnamphora can be found regularly, but scattered. Here, plants climb
among shrubs and in the forest. Sometimes the funnel shaped, small upper
pitchers can be found.
Nepenthes singalana grows in the same habitat
as Nepenthes aristolochioides, but in a different ecological niche,
as mentioned above. The type of Nepenthes singalana growing here
is usually quite small and gracile, but also single large ground-pitchers
have been found. The upper pitchers are very slender and small, while
several (but not all) ground pitchers show very distinct ribs and teeth.
Nepenthes singalana is also restricted to the mossy forest, but
single plants can also be found at somewhat lower altitudes at open places.
It is obvious that Nepenthes aristolochioides mainly produces pitchers
high up in the trees while Nepenthes singalana usually bears pitchers
at the ground on Sphagnum moss, so they colonize different ecological
niches in the same habitat. One hybrid between Nepenthes aristolochioides
and Nepenthes singalana has been found growing in Sphagnum
moss. The mouth of it was nearly vertical.
Trap Mechanism of Nepenthes aristolochioides:

Figure 3. Nepenthes aristolochioides. A)proposed trapping mechanism
of upper pitcher B)proposed trapping mechanism of lower pitcher |
The outstanding characteristic of the upper pitchers
of Nepenthes aristolochioides is the vertical position of the mouth;
in this distinctiveness it is unique within the genus Nepenthes.
This phenomenon can be found in Nepenthes klossi from Irian Jaya,
but not as extreme as in Nepenthes aristolochioides. It seems that
it is an adaptation to a special ecological niche in this species; the
species are not closely related to each other. In the pitchers of the
climbing stem of Nepenthes aristolochioides it is remarkable that
the rim and the lower surface of the lid is usually coloured dark red,
but the colour of pitchers is ivory white with red dots. The author presumes
that the trap-mechanism of the upper pitchers of Nepenthes aristolochioides
is like the mechanism in Darlingtonia californica or Sarracenia
psittacina (Sarraceniaceae): the front of the mouth is darkened by
the dark red lid and the dark red rim, but small insects are attracted
by the light which shines through the ivory white pitchers. Insects get
through the dark mouth to the shiny inner side of the pitcher, where they
do not find the way back because of the dark entrance; later on the insects
become exhausted and fall into the fluid at the ground of the pitcher
(Figure 3a). The shiny inner side of the pitcher and the dark mouth can
well be observed at Figure 1. In the field, just few small flying insects
have been found in the upper pitchers. The mechanism of the rosette-pitchers
seems to be quite different; it is striking that the utriculate pitchers
bear just an extremely small, nearly vertical mouth with an extremely
broad rim to the inner side of the pitcher. It may be something like a
wicker trap which catches small crawling insects at the ground. The inner
side of the pitcher can easily be reached by crawling insects by crawling
through the tunnel of the mouth, but once fallen into the pitcher it is
impossible to climb back through the mouth (Figure 3b). More detailed
field-observations and analysis of the captured insects may help to demonstrate
the real mechanism of these extraordinary traps.
Conservation
Nepenthes aristolochioides seems to be an extremely
endangered species because of its very small range, which is just known
from two mountains in Central Sumatra! At moment, the habitats are not
endangered by logging because both are situated in Nature Reserves, but
too enthusiastic collectors could endanger the known population dramatically.
So it remains the responsibility of all of us not to disturb such fragile
populations of Nepenthaceae. Owing to the horticultural interest in this
species, the precise locality is omitted from this description.
Acknowledgments
I would like to thank Dr. Jan Schlauer for critical reading
of this paper and Matthias Schmidt for preparing the illustrations. I
want to thank Heiko Rischer and Dr. Andreas Wistuba for helpful general
discussions. I would like to thank Mr. Andy Adek from Sumatra for his
valuable help through many years in the organization and realization of
most of our field-trips in Sumatra-Barat. I want to thank the staff and
directors of Rijksherbarium Leiden and Royal Botanic Gardens Kew for the
possibility to study the material of Nepenthaceae. Last but not least
I want to thank Katrin Hinderhofer, who accompanied me to this field-trip.
Table 1.
Because of its unique vertical mouth, Nepenthes aristolochioides
is clearly distinguished from all other species of Nepenthaceae. Nepenthes
aristolochioides shows close affinities to Nepenthes talangensis,
but this species has pitchers with a vertical mouth. Table
1 shows some characteristics which clearly distinguish Nepenthes aristolochioides
from Nepenthes talangensis.
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Characteristic
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Nepenthes aristolochioides
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Nepenthes talangensis
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mouth of upper pitchers
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vertical
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horizontal
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mouth of lower pitchers
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oblique to vertical
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horizontal
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shape of mouth
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oblique to ovate, without neck
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elevated into a short neck
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insertion of lid
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in front of the pitcher
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above the pitcher
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size of mouth in lower pitchers
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1-1.5 cm wide
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3-5 cm wide
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size of lid in lower pitchers
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1-1.5 cm in diameter
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3-4 cm in diameter,
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orientation of rim of lower pitchers:
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elongated towards the inner side of the pitcher
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around the horizontal mouth
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growing habit
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usually climbing high up into the trees or high
shrubs; with long internodes
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usually growing as rosettes or climbing in low
shrubs
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Literature:
Danser, B. H. 1928, The Nepenthaceae of the Netherlands
Indies, Bull. Jard. Bot. Buitenzorg, Serie III. Vol. IX. Livr. 3-4.
Jacobs, M. 1938, Contributions to the Botany of Mount
Kerintji and Adjacent Area in West Central Sumatra-I, Annales Bogorienses
3, 45-79.
Jebb, M. and Cheek, M. 1997, A Skeletal Revision of
Nepenthes (Nepenthaceae), Blumea 42, 1-106.
Nerz, J. and Wistuba, A. 1994, Five New Taxa of Nepenthes
(Nepenthaceae) from North and West Sumatra, Carniv. Pl. Newslett. 23,
101-114.
Figures:

Front Cover: Nepenthes aristolochioides intermediate
pitcher.

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