Nepenthes rafflesiana

Nepenthes rafflesiana (/nɪˈpɛnθz ræˌflziˈɑːnə/; after Stamford Raffles), or Raffles' pitcher-plant,[3] is a species of tropical pitcher plant. It has a very wide distribution covering Borneo, Sumatra, Peninsular Malaysia, and Singapore. Nepenthes rafflesiana is extremely variable, with numerous forms and varieties described. In Borneo alone, there are at least three distinct varieties. The giant form of this species produces enormous pitchers rivalling those of N. rajah in size.

Nepenthes rafflesiana
Nepenthes rafflesiana from Borneo.
Scientific classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Order: Caryophyllales
Family: Nepenthaceae
Genus: Nepenthes
Species:
N. rafflesiana
Binomial name
Nepenthes rafflesiana
Jack (1835)
Synonyms[2]

Distribution and habitat

Typical habitat of N. rafflesiana.

Nepenthes rafflesiana is a widespread lowland species. It is common in Borneo and parts of the Riau Archipelago, but has a restricted distribution in both Peninsular Malaysia and Sumatra. It is only widespread in the southeastern region of the Malay Peninsula, particularly in the state of Johor, where it is relatively abundant. Nepenthes rafflesiana has only been recorded from the west coast of Sumatra, between Indrapura and Barus.[4] It is also found in Singapore and on a number of smaller islands, including Bangka, Labuan,[5] Natuna,[6] and the Lingga Islands.[7]

Nepenthes rafflesiana generally occurs in open, sandy, wet areas. It has been recorded from kerangas forest, secondary formations, margins of peat swamp forest, heath forest, and seaside cliffs. It grows at elevations ranging from sea-level to 1200 m[4] or even 1500 m.[8]

Description

Detail of the peristome on a lower pitcher.

Nepenthes rafflesiana is a scrambling vine. The stem may climb to a height of 15 m and is up to 10 mm thick. Internodes are up to 20 cm long.[4] Tendrils may be over 110 cm long.

The lower pitchers of N. rafflesiana are bulbous and possess well-developed fringed wings. These terrestrial traps rarely exceed 20 cm in height, although the giant form of N. rafflesiana is known produce pitchers up to 35 cm long and 15 cm wide. Upper pitchers are funnel-shaped and often bear a distinctive raised section at the front of the peristome. Both types of pitchers have a characteristically elongated peristome neck that may be 3 cm or more in length.

Pitcher colouration varies greatly from dark purple to almost completely white. The typical form of N. rafflesiana is light green throughout with heavy purple blotches on the lower pitchers and cream-coloured aerial pitchers.

The inflorescence is a raceme and grows between 16 and 70 cm tall. The red or purple flowers usually occur singly, or sometimes in pairs, on each flower-stalk.

Young plants are wholly covered with long, caducous, brown or white hairs. Mature plants often have a sparse indumentum of short, brown hairs, though they may be completely glabrous.

Biology

Ant drinking nectar from the peristome of a N. rafflesiana pitcher

Nepenthes rafflesiana is found in tropical lowlands. It produces two distinct types of pitchers (heavily modified leaves), which are used to capture and kill insect prey for nutrients. The lower pitchers are generally round, squat and 'winged', while the upper pitchers are more narrow at their base. The species is widely variable and comes in a variety of shapes and colors – most contain varying amounts of green, white, and maroon streaks.

All Nepenthes are passive carnivores with no moving parts, unlike their distant cousins the Venus flytrap. Nepenthes rafflesiana kills by luring its prey into its pitchers, whose peristomes secrete a sweet-tasting nectar. Once the insect is inside, it quickly finds the walls of the pitcher too slippery to scale and drowns. Digestive enzymes released by the plant into the liquid break down the prey and release soluble nutrients, which are absorbed by the plant through the walls of the pitcher. The carnivorous nature of Nepenthes is supposedly a consequence of living in nutrient-poor soils; since the main method of nutrient absorption in most plants (the root) is insufficient in these soils, the plants have evolved other ways to gain nutrients. As a result, the roots of Nepenthes and most other carnivorous plants are slight and fragile; hence care must be taken when repotting. All Nepenthes are dioecious, meaning that each individual plant has only male or female characteristics.

For Nepenthes pitchers being used as daytime roosting sleeping bags by small bats, see Nepenthes hemsleyana#Relationship with bats.

Discovery and early history

Nepenthes rafflesiana cultivated in England as illustrated in The Gardeners' Chronicle and Agricultural Gazette, 1872.

Nepenthes rafflesiana was discovered by Dr. William Jack in 1819. In a letter from Singapore published in Curtis's Botanical Magazine, Jack wrote the following account:[3]

It is impossible to conceive anything more beautiful than the approach to Singapore, through the Archipelago of islands that lie at the extremity of the Straits of Malacca. Seas of glass wind among innumerable islets, clothed in all the luxuriance of tropical vegetation and basking in the full brilliance of a tropical sky... I have just arrived in time to explore the woods before they yield to the axe, and have made many interesting discoveries, particularly of two new and splendid species of pitcher-plant [Nepenthes rafflesiana and Nepenthes ampullaria], far surpassing any yet known in Europe. I have completed two perfect drawings of them with ample descriptions. Sir S. Raffles is anxious that we should give publicity to our researches in one way or other and has planned bringing out something at Bencoolen. He proposes sending home these pitcher-plants that such splendid things may appear under all the advantages of elegant execution, by way of attracting attention to the subject of Sumatran botany.

At the time the largest known species in the genus, N. rafflesiana was described in the Gardener's and Farmer's Journal for 1850 as follows:[3]

Whoever has seen this plant in a living state must undoubted be constrained to consider it as one of the most astonishing productions of the whole vegetable kingdom. The resemblance that a portion of it bears to our more familiar domestic utensils leaves a lasting impression on the minds of spectators that is not easily eradicated; it is the largest and most magnificent of the genus, far surpassing any hitherto known in Europe.

Cultivation

Nepenthes rafflesiana is very popular in cultivation; it is a lowland Nepenthes (enjoying hot, humid conditions most of the time, as found in tropical jungle lowlands) but can be grown as an intermediate, with cooler nights and less humidity. It is a comparatively hardy Nepenthes that is commonly recommended as a "first plant" to new Nepenthes growers. The plant should be grown in shaded conditions, diffuse sunlight, or in a large grow chamber under artificial lights. Watering and misting should be performed frequently, and preferably with distilled water, to avoid mineral build-up that is not only unsightly but that may damage the delicate roots of Nepenthes (and most other carnivorous plants). Standing water is inadvisable. A wet, well-draining potting medium is a necessity. Methods of feeding are varied – some growers feed freeze-dried bloodworms or Koi pellets (both available in the fish section of most pet stores); others prefer orchid mixes. No carnivorous plant should ever be fed mammalian meat – this will result not only in an unpleasant smell but also the probable rotting of the pitcher and potential death of the plant. The digestive enzymes present have not evolved to handle large prey items, and the rotting material gives opportunistic bacteria and fungi a chance to take hold.

Infraspecific taxa

Left: Nepenthes rafflesiana var. insignis, an apparently "large-pitchered variety with unusually dark purple markings",[3] as illustrated in The Gardeners' Chronicle, 1882
Right: A lower pitcher of N. hemsleyana, previously known under a variety of names including N. rafflesiana var. elongata and N. baramensis

Across its expansive range, N. rafflesiana exhibits great variability in both pitcher morphology and colour. The following infraspecific taxa of N. rafflesiana have appeared in the literature. Most of these are not considered valid today, and a number represent different taxa altogether. The elongate plant often referred to informally as N. rafflesiana var. elongata, and described as N. baramensis,[9] is now known under the name N. hemsleyana.[10]

Giant form

Vegetative parts of the giant form (from left to right): a lower pitcher measuring over 30 cm; a tendril measuring over 110 cm; and an upper pitcher measuring around 45 cm.

Giant plants of N. rafflesiana have been recorded from a number of isolated localities on the northwestern coast of Borneo and one population has been found near the seaside town of Sematan, around 110 km west of Kuching.[16] The typical habitat of this form is dense heath forest, especially around vegetation boundaries.[16]

The giant form is a much larger plant than the typical form in all respects. The stem may climb to a height of 15 m. Leaf blades are around two and a half times as long as usual. Lower pitchers reach 35 cm in height by 15 cm in width and sometimes exceed 1 litre in volume, making them some of the largest in the genus.[16] They vary widely in pigmentation, from white with red blotches to dark purple. Upper pitchers may be spotted or green throughout. The inflorescence is also massive, reaching over 1 m in length. The individual flowers measure up to 1.5 cm in diameter and have dark red tepals.[16]

In addition to its size, the giant form is distinguished by the colour of its developing leaves, which have a bronze sheen. Both this characteristic and the plant's exceptional size are exhibited by cultivated specimens and thus they cannot be due to unusual environmental factors.[16]

Natural hybrids

The following natural hybrids involving N. rafflesiana have been recorded.

Conservation

N. rafflesiana growing in a previously logged area.

Most wild populations of Nepenthes, including N. rafflesiana, are endangered due to habitat destruction and (to a lesser extent) poaching. N. rafflesiana is currently listed as a CITES Appendix II plant, so it does have some international trade restrictions (though not an outright ban). Today, most N. rafflesiana plants on the market are propagated by plant tissue culture or other forms of vegetative propagation. When purchasing any plant, especially those protected by CITES, it is important to ask the vendor about the plant's provenance.

References

This illustration of N. rafflesiana by Walter Hood Fitch appeared in Curtis's Botanical Magazine in 1847.
  1. Clarke, C.M. (2018). "Nepenthes rafflesiana". IUCN Red List of Threatened Species. 2018: e.T39689A143963510. Retrieved 30 June 2020.
  2. Schlauer, J. N.d. Nepenthes rafflesiana. Carnivorous Plant Database.
  3. Phillipps, A. & A. Lamb 1996. Pitcher-Plants of Borneo. Natural History Publications (Borneo), Kota Kinabalu.
  4. Clarke, C.M. 2001. Nepenthes of Sumatra and Peninsular Malaysia. Natural History Publications (Borneo), Kota Kinabalu.
  5. Burbidge, F.W. 1882. Notes on the new Nepenthes. The Gardeners' Chronicle, new series, 17(420): 56.
  6. (in Indonesian) Mansur, M. 2012. Keanekaragaman jenis tumbuhan pemakan serangga dan laju fotosintesisnya di Pulau Natuna. [Diversity on insectivorous plants and its photosynthetic rate in Natuna Island.] Berita Biologi 11(1): 33–42. Abstract Archived 2013-09-21 at the Wayback Machine
  7. Clarke, C.M. 2001. Appendix C: Distribution Maps. In: Nepenthes of Sumatra and Peninsular Malaysia. Natural History Publications (Borneo), Kota Kinabalu. pp. 299–307.
  8. Adam, J.H., C.C. Wilcock & M.D. Swaine 1992. "The ecology and distribution of Bornean Nepenthes" (PDF). Archived from the original (PDF) on 2011-07-22. Journal of Tropical Forest Science 5(1): 13–25.
  9. Clarke, C., J.A. Moran & C.C. Lee 2011. Nepenthes baramensis (Nepenthaceae) – a new species from north-western Borneo. Blumea 56(3): 229–233. doi:10.3767/000651911X607121
  10. Scharmann, M. & T.U. Grafe 2013. Reinstatement of Nepenthes hemsleyana (Nepenthaceae), an endemic pitcher plant from Borneo, with a discussion of associated Nepenthes taxa. Blumea 58(1): 8–12. doi:10.3767/000651913X668465
  11. (in German) Beck, G. 1895. Die Gattung Nepenthes. Wiener Illustrirte Garten-Zeitung 20(3–6): 96–107, 141–150, 182–192, 217–229.
  12. (in Latin) Hooker, J.D. 1873. Ordo CLXXV bis. Nepenthaceæ. In: A. de Candolle Prodromus Systematis Naturalis Regni Vegetabilis 17: 90–105.
  13. Clarke, C.[M.] 1997. Another Nice Trip to Sumatra. Carnivorous Plant Newsletter 26(1): 4–10.
  14. (in French) Teysmann, M.J.E. 1859. Énumération des plantes envoyées de Java au jardin botanique de l'Université de Leide. Annales d'horticulture et de botanique, ou Flore des jardins du royaume des Pays-Bas, et histoire des plantes cultivées les plus intéressantes des possessions néerlandaises aux Indes orientales, de l'Amérique et du Japon 2: 133–142.
  15. Burbidge, F.W. 1880. The Gardens of the Sun. Murray, London.
  16. Clarke, C.M. 1997. Nepenthes of Borneo. Natural History Publications (Borneo), Kota Kinabalu.
  17. Lowrie, A. 1983. "Sabah Nepenthes Expeditions 1982 & 1983" (PDF). (1.25 MiB) Carnivorous Plant Newsletter 12(4): 88–95.
  18. McPherson, S.R. 2009. Pitcher Plants of the Old World. 2 volumes. Redfern Natural History Productions, Poole.
  19. Masters, M.T. 1881. New garden plants. Nepenthes Hookeriana. The Gardeners' Chronicle, new series, 16(417): 812–813.
  20. Yulita, K.S. & M. Mansur 2012. The occurrence of hybrid in Nepenthes hookeriana Lindl. from Central Kalimantan can be detected by RAPD and ISSR markers. HAYATI Journal of Biosciences 19(1): 18–24. doi:10.4308/hjb.19.1.18
  21. Phillipps, A., A. Lamb & C.C. Lee 2008. Pitcher Plants of Borneo. Second Edition. Natural History Publications (Borneo), Kota Kinabalu.
  22. Tan, W.K., C.L. Wong & C.K. Frazier 1996. Nepenthes × (rafflesiana and gracilis)? Nature Malaysiana 21: 82–85.
  23. Bednar, B.L. 1985. "Nepenthesdominii and var. intermedia" (PDF). Carnivorous Plant Newsletter 14(4): 105–106.

Further reading

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