The first known collection of N. spectabilis was made by Julius August Lörzing in 1920. The specimen Lörzing 7308 was collected on June 5, 1920, on Mount Sibajak at an elevation of 1800 to 1900 m. It is deposited at the Bogor Botanical Gardens (formerly the Herbarium of the Buitenzorg Botanic Gardens) along with two isotypes which include both male and female floral material. A third isotype, sheet H.L.B. 928.350-170,[3] is held at the National Herbarium of the Netherlands in Leiden and includes female floral material.[2][4]
This new species has only been found on the G. Sibajak and the G. Pinto, two tops of the same mountain ; the Bt. Semaik too certainly belongs to the same group. N. spectabilis grows above 1800 m elevation ; the habitat is alpine forest and scrub. It seems to be most closely related to N. sanguinea by the characters of the vegetative parts, but the inflorescences are quite different.
Lörzing says of his number 8297 that it was a monoeceous [sic] plant ; since, however, in H. B. there is no stem fragment both with male and female flowers, I call this record into question.
The next major taxonomic treatment of N. spectabilis came only in 1986, when Rusjdi Tamin and Mitsuru Hotta covered the species in their monograph on the Nepenthes of Sumatra.[5]
In their 1997 revision of the genus, Matthew Jebb and Martin Cheek treated specimens of N. lavicola as belonging to N. spectabilis. They also designated Lörzing 7308 as the lectotype of N. spectabilis.[8] The subsequent monograph of Charles Clarke treats these taxa as distinct species.[2]
Description
Nepenthes spectabilis is a climbing plant. The stem can reach lengths of 6 m and is up to 7 mm in diameter. Internodes are cylindrical in cross section and up to 10 cm long.[2]
Leaves are coriaceous and sessile. The lamina is oblong and up to 16 cm long by 6 cm wide. It has a rounded-acute apex and is gradually attenuate towards the base. Up to 6 longitudinal veins are present on either side of the midrib. Pinnate veins are usually indistinct. Tendrils are up to 25 cm long.[2]
Rosette and lower pitchers are narrowly ovoid in the lower third to half of the pitcher cup. Above the hip, they are cylindrical and somewhat narrower. Terrestrial pitchers are relatively small, growing to 12 cm in height and 4 cm in width. A pair of fringed wings (≤4 mm wide) runs down the front of the pitcher. The glandular region covers the ovoid portion of the pitcher's inner surface;[2] the waxy zone above is well developed.[9] The mouth is round and flat at the front, becoming oblique towards the lid. The peristome is cylindrical in cross section and up to 4 mm wide. Its inner margin is lined with small but distinct teeth.[2] The inner portion of the peristome accounts for around 41% of its total cross-sectional surface length.[9] The pitcher lid or operculum is sub-orbicular in shape, lacks appendages, and has a strongly cordate base. The spur is very long (≤30 mm) and unbranched. It is inserted near the base of the lid.[2]
A typical upper pitcher of N. spectabilis (left) and one of a particularly gracile form of this species (right)
Upper pitchers arise gradually from the end of the tendril. They are very narrowly infundibular in the lower half to three-quarters. Above the hip, they are either cylindrical or narrowly infundibular. Aerial pitchers are much larger than their terrestrial counterparts, growing to 26 cm in height and 4.5 cm in width.[4] They usually have ribs in place of wings, although fringe elements may be present near the peristome. The glandular region covers the inner surface below the hip. The pitcher mouth is round and has a steeply oblique insertion. The peristome is cylindrical and up to 3 mm wide. Other parts of the upper pitchers are similar to those of the lower pitchers.[2]
Nepenthes spectabilis has a racemoseinflorescence. The peduncle grows to 12 cm in length. The rachis may be up to 15 cm long, although it is usually shorter and denser in female inflorescences. Partial peduncles are bracteolate and two-flowered. Sepals are elliptic-oblong in shape and up to 5 mm long.[2]
Nepenthes spectabilis exhibits considerable variation in the development of its indumentum. In most plants, developing parts are covered in short, stellate reddish-brown hairs, although many of these are caducous. Inflorescences and the margins of the lamina bear dense, stellate reddish-brown hairs that are persistent. A dense covering of short, persistent hairs is also present on the lower surface of the midrib.[2]
The stem and lamina are green. Pitchers are characteristically light green with numerous dark brown speckles. The peristome is often yellowish-green with brown stripes.[2]
Certain populations of N. spectabilis differ considerably in morphology. Plants from the type locality produce relatively broad upper pitchers, while those from Mount Pangulubao are much narrower. A particularly gracile form has been recorded from the west side of Lake Toba. Plants from Mount Siluatan are different still, producing pitchers that are green throughout. The species also exhibits great variability in the extent of the indumentum; some plants have a dense covering of hairs, while others are virtually glabrous.[2][10]
Due to the patchy distribution of N. spectabilis, its conservation status is listed as Vulnerable on the 2006 IUCN Red List of Threatened Species.[1] Upon observing N. spectabilis on Mount Pangulubao in 1995, botanist Charles Clarke wrote that he "got the impression that collectors had taken a bit of a toll on the population, partly because very few immature plants were visible".[15]
Related species
Nepenthes spectabilis is thought to be most closely related to N. lavicola. It can be distinguished from that species on the basis of its smaller floral bracts, longer fruits, and very long unbranched spur.[2] In addition, the species differ in the shape of their lower pitchers. Those of N. lavicola are urceolate to globose, while those of N. spectabilis are ovoid in the lower part and cylindrical above. Furthermore, the pitchers of N. lavicola are generally dark brown or purple throughout, compared to the light green and dark brown speckled traps of N. spectabilis.[3]
In Nepenthes of Sumatra and Peninsular Malaysia, Charles Clarke mentions an undescribed taxon from Aceh that is intermediate in appearance between N. lavicola and N. spectabilis. It is unlikely to be of hybridogenic origin as it is not sympatric with any other Nepenthes species.[2]
Nepenthes rigidifolia also bears a superficial resemblance to N. spectabilis, particularly in the colouration of its pitchers.[2] Apart from its markedly different upper pitchers, N. spectabilis differs from the former in having thin leaves, an unbranched spur, and an apical tendril insertion.[16]
The third group, that of the Nobiles, comprises the species that form a transition between the Vulgatae and the Montanae on one hand and the Regiae on the other. N. spectabilis, from Sumatra, reminds one of N. sanguinea in many respects but shows a resemblance with the Regiae by the yellowish colour of herbarium specimens and by the red-brown indumentum.
Clarke suggests that N. spectabilis "would perhaps have been better placed in the Montanae, which includes several species that appear to be closely related, such as N. gymnamphora and N. pectinata".[2]
In 2001, Clarke published a cladistic analysis of the Nepenthes species of Sumatra and Peninsular Malaysia based on 70 morphological characteristics of each taxon. The resultant cladogram placed N. spectabilis in a small clade with N. gymnamphora. However, since the study was limited in its geographical scope, this placement may not accurately reflect the relationship between N. spectabilis and its closest relatives.[2]
Natural hybrids
A lower pitcher of N. ovata × N. spectabilis (left) and a lower pitcher of N. rigidifolia × N. spectabilis (right)
A lower pitcher of N. rhombicaulis × N. spectabilis (left) and a lower pitcher of a possible natural cross between N. gymnamphora and N. spectabilis (right)
Nepenthes spectabilis occurs sympatrically with many other Nepenthes species and a number of natural hybrids have been recorded.[2]
N. ovata × N. spectabilis
Nepenthes ovata × N. spectabilis is known to occur along the summit trail of Mount Pangulubao. This hybrid produces pitchers roughly intermediate in appearance between its parent species. The peristome is flattened and expanded, but to a lesser degree than in N. ovata. The speckles of N. spectabilis are present, but the pitchers have a much lighter colouration. Most examples of this hybrid grow terrestrially and some climb into the forest canopy.[2]
N. rigidifolia × N. spectabilis
Several plants representing the cross N. rigidifolia × N. spectabilis have been recorded from an open rocky outcrop close to the type locality of N. rigidifolia. The hybrid differs from N. rigidifolia in having narrower pitchers with an infundibular base and distinct hip around the middle. On the other hand, the pitchers of this hybrid are broader than those of N. spectabilis and have a wider, expanded peristome.[2]
The richly coloured lower pitchers of N. rigidifolia × N. spectabilis superficially resemble those of N. macfarlanei. However, since that species is confined to Peninsular Malaysia, the two taxa are not easily confused.[2]
Other hybrids
Four other natural hybrids with N. spectabilis have been recorded. These are N. gymnamphora × N. spectabilis, N. mikei × N. spectabilis, N. rhombicaulis × N. spectabilis, and N. spectabilis × N. tobaica.[2]
Notes
^Lörzing 8260 was collected near the summit of Mount Pinto on January 22, 1921, at an elevation of 2100 to 2200 m. It is deposited at the Bogor Botanical Gardens and includes male floral material. A doubtful duplicate specimen is held at the National Herbarium of the Netherlands and also includes male floral material.[4] Lörzing 8297 was collected on Mount Sibajak on January 23, 1921, at an elevation of 1900 m. It is deposited at the Bogor Botanical Gardens and includes both male and female floral material.[4]
^ The original Latin description of N. spectabilis reads:[4]
Folia mediocria sessilia v. petiolo late alato, lamina oblonga-spathulata, nervis longitudinalibus utrinque 5-6, basi rotundata v. leviter cordata caulis 2/3-3/4 amplectente, vagina 0, ascidia rosularum et inferiore ignota ; ascidia superiore magna, e parte inferiore anguste infundibuliformi tubulosa ; costis 2 prominentibus ad os appendice folicea ramosa ornatis ; peristomio operculum versus accuminato, vix in collum elongato applanato, 3-12 mm lato, costis 3/4-1 mm distantibus, dentibus 3-5 x longioribus quam latis ; operculo rotundato-cordato, facie inferiore plano v. obtusa-cordato inflorescentia racemus pedicellis 10-3 mm longis plerumque 2-floris ; indumentum parcum villoso-tomentosum, ferrugineum.
^(in Indonesian) Tamin, R. & M. Hotta 1986. Nepenthes di Sumatera: The genus Nepenthes of the Sumatra Island. In: M. Hotta (ed.) Diversity and Dynamics of Plant Life in Sumatra: Forest Ecosystem and Speciation in Wet Tropical Environments. Part 1: Reports and Collection of Papers. Kyoto University, Kyoto. pp. 75–109.
^ abBauer, U., C.J. Clemente, T. Renner & W. Federle 2012. Form follows function: morphological diversification and alternative trapping strategies in carnivorous Nepenthes pitcher plants. Journal of Evolutionary Biology25(1): 90–102. doi:10.1111/j.1420-9101.2011.02406.x
Bonhomme, V., H. Pelloux-Prayer, E. Jousselin, Y. Forterre, J.-J. Labat & L. Gaume 2011. Slippery or sticky? Functional diversity in the trapping strategy of Nepenthes carnivorous plants. New Phytologist191(2): 545–554. doi:10.1111/j.1469-8137.2011.03696.x
Meimberg, H., A. Wistuba, P. Dittrich & G. Heubl 2001. Molecular phylogeny of Nepenthaceae based on cladistic analysis of plastid trnK intron sequence data. Plant Biology3(2): 164–175. doi:10.1055/s-2001-12897
Meimberg, H. & G. Heubl 2006. Introduction of a nuclear marker for phylogenetic analysis of Nepenthaceae. Plant Biology8(6): 831–840. doi:10.1055/s-2006-924676
Meimberg, H., S. Thalhammer, A. Brachmann & G. Heubl 2006. Comparative analysis of a translocated copy of the trnK intron in carnivorous family Nepenthaceae. Molecular Phylogenetics and Evolution39(2): 478–490. doi:10.1016/j.ympev.2005.11.023
Renner, T. & C.D. Specht 2011. A sticky situation: assessing adaptations for plant carnivory in the Caryophyllales by means of stochastic character mapping. International Journal of Plant Sciences172(7): 889–901. doi:10.1086/660882
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