The species was collected by Hugh Low on Mount Kinabalu in 1858, and described the next year by Joseph Dalton Hooker, who named it after James Brooke, the first White Rajah of Sarawak. Since being introduced into cultivation in 1881, it has always been a sought-after species, although costly and hard to cultivate. Tissue culture has allowed it to become more widespread in cultivation.
N. rajah is best known for the giant urn-shaped traps it produces, which can grow up to 41 cm (16 in) high and 20 cm (7.9 in) wide. These are capable of holding 3.5 L (0.92 US gal) of water and in excess of 2.5 L (0.66 US gal) of digestive fluid, making them probably the largest in the genus.
N. rajah can trap mammals as large as rats. N. rajah occasionally traps small vertebrates such as frogs, lizards, and even birds. Insects, and particularly ants, are its staple prey. The pitchers are host to many other organisms, some so specialised that they cannot survive anywhere else, and are called nepenthebionts. N. rajah has two such mosquitotaxa named after it: Culex rajah and Toxorhynchites rajah. The species is able to hybridise in the wild with all other locally-occurring Nepenthes species.
Etymology
Joseph Dalton Hooker described Nepenthes rajah in 1859, naming it in honour of James Brooke, the first White Rajah of Sarawak. 'Rajah Brooke's Pitcher Plant' is an accurate, but seldom-used common name. N. rajah is sometimes called the 'Giant Malaysian Pitcher Plant' or simply 'Giant Pitcher Plant', although the binomial name remains by far the most popular way of referring to this species. The specific epithetrajah means "King" in Malay and this, coupled with the impressive size of its pitchers, has meant that N. rajah is often called the "King of Nepenthes".
Nepenthes rajah is a scrambling vine. The stem usually grows along the ground, but climbs whenever it comes into contact with a suitable support. The stem is up to 30 mm (1.2 in)) thick and may reach up to 6 m (20 ft) in length, although it rarely exceeds 3 m (9.8 ft). The leaves are distinctive and reach a large size. They are leathery in texture with a wavy outer margin. The leaves are characteristically peltate, whereby the tendril joins the lamina on the underside, before the apex. The tendrils are inserted within 5 cm (2.0 in) below the leaf apex and reach a length of approximately 50 cm (20 in).
Pitchers
The pitcher is a trap consisting of the main pitcher cup, covered by an operculum or lid. A reflexed ring of hardened tissue, the peristome, surrounds the entrance. N. rajah produces two distinct types of trap. "Lower" or "terrestrial" pitchers, the most common, are very large, richly coloured, and ovoid in shape. Exceptional specimens may be more than 40 cm (16 in) in length and hold 3.5 L (0.92 US gal) of water and over 2.5 L (0.66 US gal) of digestive fluid, although most do not exceed 200 ml (6.8 U.S. fl oz). The lower pitchers rest on the ground. They are usually red to purple on the outside, lime green to purple on the inside. Mature plants may in addition produce much smaller "upper" or "aerial" pitchers, which are funnel-shaped, and usually more colourful. The tendril attachment is normally at the rear of the pitcher cup. True upper pitchers are rare, as the stems rarely attain lengths greater than a few metres before dying off.
The peristome has a distinctive scalloped edge and is greatly expanded, forming a red lip around the trap's mouth. A series of raised ribs intersect the peristome, ending in short, sharp teeth that line its inner margin. The inner portion of the peristome accounts for around 80% of its total cross-sectional surface length. The huge, vaulted lid is a distinguishing feature of this species. It is ovate to oblong in shape with a distinct keel down the middle, and two prominent lateral veins. The spur at the back of the lid is approximately 20 mm (0.79 in) long and unbranched.
The plant has very large nectar-secretingglands covering its pitchers. The inner surface of the pitcher is wholly glandular, with 300 to 800 glands/cm (1,900 to 5,200 glands/in).
Flowers
N. rajah seems to flower at any time of the year. Flowers are produced in large numbers on inflorescences that arise from the apex of the main stem. N. rajah produces a very large inflorescence that can be 80 cm (31 in), and sometimes even 120 cm (47 in) tall. The individual flowers of N. rajah are produced on partial peduncles (twin stalks) and so the inflorescence is called a raceme (as opposed to a panicle for multi-flowered bunches). The flowers are reported to give off a strong sugary smell and are brownish-yellow in colour. Sepals are elliptic to oblong and up to 8 mm (0.31 in) long. Like all Nepenthes species, N. rajah is dioecious, which means that individual plants produce flowers of a single sex. Fruits are orange-brown and 10 to 20 mm (0.39 to 0.79 in) long . A study of 300 pollen samples taken from a herbarium specimen (J.H.Adam 2443, collected at an altitude of 1,930–2,320 m (6,330–7,610 ft)) found the mean pollen diameter to be 34.7 μm (0.00137 in) (SE = 0.3; CV = 7.0%).
Mature plants with both lower and upper pitchers
The peltate leaf attachment
A terrestrial pitcher
The 41 cm (16 in) pitcher found on The Sabah Society's March 2011 trip to Mesilau
N. rajah is a carnivorous plant of the pitfall trap variety. It is famous for occasionally trapping vertebrates, even small mammals. There exist at least two records of drowned rats found in N. rajah pitchers. The first observation dates from 1862 and was made by Spenser St. John, who accompanied Hugh Low on two ascents of Mount Kinabalu. In 1988, Anthea Phillipps and Anthony Lamb confirmed the plausibility of this record when they managed to observe drowned rats in a large pitcher of N. rajah. In 2011, a drowned mountain treeshrew (Tupaia montana) in a N. rajah pitcher was reported. N. rajah occasionally traps other small vertebrates, including frogs, lizards and even birds, although these cases probably involve sick animals, or those seeking shelter or water in the pitcher, and certainly do not represent the norm. Insects, and particularly ants, comprise the majority of prey in both aerial and terrestrial pitchers.
Mutualism with mammals
Nepenthes rajah has evolved a mutualistic relationship with mountain treeshrews (Tupaia montana) in order to collect their droppings. The inside of the reflexed lid exudes a sweet nectar. The distance from the pitcher mouth to the exudate is the same as the average body length of the mountain treeshrew. As it feeds, the treeshrew defecates, apparently as a method of marking its feeding territory. It is thought that in exchange for providing nectar, the faeces provide the plant with the majority of the nitrogen it requires. In N. lowii, N. macrophylla and N. ;rajah, the colour of the lower lid surface corresponds to visual sensitivity maxima of the mountain treeshrew in the green and blue wavebands, making the lid underside stand out against adjacent parts of the pitcher. Of the three species, N. rajah shows the tightest 'fit', particularly in the green waveband.
In 2011, it was reported that N. rajah has a similar mutualistic relationship with the summit rat (Rattus baluensis). Whereas the mountain treeshrew visits pitchers during daylight hours, the summit rat is primarily active at night; this may be an example of resource partitioning. Daily scat deposition rates were found to be similar for both mammalian species.
Left: Mammal visitation rates to N. rajah pitchers. White bars show visitation by T. montana and black bars by R. baluensis. The horizontal bar below the x-axis indicates photoperiod, white representing daylight hours and black nighttime. Right: Scat deposition rates to N. rajah pitchers. Black squares show the mean number of T. montana droppings found within pitchers; white squares show the mean number found outside pitchers. Black and white diamonds show the same for R. baluensis.
Although Nepenthes are most famous for trapping and digesting animals, their pitchers play host to a large number of other organisms (known as infauna). These include fly and midgelarvae, spiders (crab spiders such as Henriksenia labuanica), mites, ants, and even a species of crab, Geosesarma malayanum. The most common and conspicuous predators found in pitchers are mosquito larvae, which consume large numbers of other larvae during their development. Many of these animals are so specialised that they cannot survive anywhere else, and are referred to as nepenthebionts.
The complex relationships between these various organisms are not yet fully understood. The question of whether infaunal animals "steal" food from their hosts, or whether they are involved in a mutually beneficial (symbiotic) association has yet to be investigated experimentally and is the source of considerable debate. Clarke suggests that mutualism is a "likely situation", whereby "the infauna receives domicile, protection and food from the plant, while in return, the infauna helps to break down the prey, increase the rate of digestion and keep bacterial numbers low".
Species specific
As the size and shape of Nepenthes pitchers vary greatly between species, but little within a given taxon, it is not surprising that many infaunal organisms are specially adapted to life in only the traps of particular species. N. rajah is no exception, and in fact has two mosquito taxa named after it. Culex (Culiciomyia) rajah and Toxorhynchites (Toxorhynchites) rajah were described by Masuhisa Tsukamoto in 1989, based on larvae collected in pitchers of N. rajah on Mount Kinabalu three years earlier. The two species were found to live in association with larvae of Culex (Lophoceraomyia) jenseni, Uranotaenia (Pseudoficalbia) moultoni and an undescribed taxon, Tripteroides (Rachionotomyia) sp. No. 2. Concerning C. rajah, Tsukamoto noted that the "body surface of most larvae are covered in Vorticella-like protozoa".
Another species, Culex shebbearei, has been recorded as an infaunal organism of N. rajah. The original 1931 record by F. W. Edwards is based on a collection by H. M. Pendlebury in 1929 from a plant growing on Mount Kinabalu. However, Tsukamoto notes that in light of new information on these species, "it seems more likely to conclude that the species [C. rajah] is a new species which has been misidentitied as C. shebbearei for a long time, rather than to think that both C. shebbearei and C. rajah n. sp. are living in pitchers of Nepenthes rajah on Mt. Kinabalu".
Pests
Not all interactions between Nepenthes and fauna are beneficial to the plant. N. rajah is sometimes attacked by insects which feed on its leaves and damage substantial portions of the lamina. Monkeys and tarsiers occasionally rip pitchers open to feed on their contents.
History and popularity
Due to its size, unusual morphology and striking coloration, N. rajah is a popular insectivorous plant. However, it remains a little-known species outside the field of carnivorous plants. Due to its specialised growing requirements, it is not a suitable houseplant and, as such, is only cultivated by hobbyists and professional growers. Its reputation for producing some of the most magnificent pitchers in the genus dates back to the late 19th century. N. rajah was first collected by Hugh Low on Mount Kinabalu in 1858. It was described the following year by Joseph Dalton Hooker, who named it after James Brooke, the first White Rajah of Sarawak. The description was published in The Transactions of the Linnean Society of London.
Spenser St. John wrote an account of his encounter with N. rajah on Mount Kinabalu in his 1862 Life in the Forests of the Far East. N. rajah was first collected for the Veitch Nurseries by Frederick William Burbidge in 1878, during his second trip to Borneo. Shortly after being introduced into cultivation in 1881, N. rajah proved very popular among wealthy Victorianhorticulturalists and became a much sought-after species. A note in The Gardeners' Chronicle of 1881 mentions the Veitch plant as follows: "N. rajah at present is only a young Rajah, what it will become was lately illustrated in our columns...". A year later, young N. rajah plants were displayed at the Royal Horticultural Society's annual show for the first time. The specimen exhibited at the show by the Veitch Nurseries, the first of this species to be cultivated in Europe, won a first class certificate. In Veitch's catalogue for 1889, N. rajah was priced at £2.2s per plant.
Dwindling interest in Nepenthes at the turn of the century saw the demise of the Veitch Nurseries and consequently the loss of several species and hybrids in cultivation, including N. northiana and N. rajah. By 1905, the final N. rajah specimens from the Veitch nurseries were gone, as the cultural requirements of the plants proved too difficult to reproduce. The last surviving N. rajah in cultivation at this time was at the National Botanic Gardens at Glasnevin in Ireland, however this soon perished also.
The first N. rajah plant cultivated in Europe, in The Garden, 1882
Click [show] to view a list of early publications, illustrations, and collections of Nepenthes rajah.
Early publications: Transact. Linn. Soc., XXII, p. 421 t. LXXII (1859); MIQ., Ill., p. 8 (1870); HOOK. F., in D.C., Prodr., XVII, p. 95 (1873); MAST., Gard. Chron., 1881, 2, p. 492 (1881); BURB., Gard. Chron., 1882, 1, p. 56 (1882); REG., Gartenfl., XXXII, p. 213, ic. p. 214 (1883); BECC., Mal., III, p. 3 & 8 (1886); WUNSCHM., in ENGL. & PRANTL, Nat. Pflanzenfam., III, 2, p. 260 (1891); STAPF, Transact. Linn. Soc., ser. 2, bot., IV, p. 217 (1894); BECK, Wien. Ill. Gartenz., 1895, p. 142, ic. 1 (1895); MOTT., Dict., III, p. 451 (1896); VEITCH, Journ. Roy. Hort. Soc., XXI, p. 234 (1897); BOERL., Handl., III, 1, p. 54 (1900); HEMSL., Bot. Mag., t. 8017 (1905); Gard. Chron., 1905, 2, p. 241 (1905); MACF., in ENGL., Pflanzenr., IV, 111, p. 46 (1908); in BAIL., Cycl., IV, p. 2129, ic. 2462, 3 (1919); MERR., Bibl. Enum. Born., p. 284 (1921); DANS., Trop. Nat., XVI, p. 202, ic. 7 (1927).
Early illustrations: Transact. Linn. Soc., XXII, t. LXXII (1859) optima; Gard. Chron., 1881, 2, p. 493 (1881) bona, asc. 1; Gartenfl., 1883, p. 214 (1883) bona, asc. 1; Wien. Ill. Gartenfl., 1895, p. 143, ic. 1 (1895) asc. 1; Journ. Roy. Hort. Soc., XXI, p. 228 (1897) optima; Bot. Mag., t. 8017 (1905) optima; BAIL., Cycl., IV, ic. 2462, 3 (1919) asc. 1; Trop. Nat., XVI, p. 203 (1927) asc. 1.
Early collections: North Borneo. Mt. Kinabalu, IX 1913, Herbarium of the Sarawak Museum (material without flowers or fruits); Marai-parai Spur, 1-4 XII 1915, Clemens 11073, Herbarium Bogoriense, the Herbarium of the Buitenzorg Botanic Gardens (male and female material); 1650 m, 1892, Haviland 1812/1852, Herbarium of the Sarawak Museum (male and female material).
Recent popularity
N. rajah is relatively well known in Malaysia, especially its native Sabah. The species is used to promote Sabah's Kinabalu National Park and features on postcards from the region. N. rajah has appeared on the covers of Nepenthes publications, including Nepenthes of Mount Kinabalu (Kurata, 1976) and Nepenthes of Borneo (Clarke, 1997), both published in Kota Kinabalu. In 1996, Malaysia issued a series of four postage stamps including one of N. rajah. N. rajah was featured in the first episode of Kingdom of Plants 3D, a natural history series presented by David Attenborough.
N. rajah grows exclusively on serpentine soils with high concentrations of nickel and chromium, toxic to many plant species. This means that it faces less competition for space and nutrients.
Mount Kinabalu, Borneo
Ultramafic outcrops (yellow) in Kinabalu National Park (green)
Climate
N. rajah has an altitudinaldistribution of 1,500–2,650 m (4,920–8,690 ft) above sea level and is thus considered an (ultra) highland or Upper Montane plant. In the upper limit of its range, night-time temperatures may approach freezing and day-time maxima rarely exceed 25 °C (77 °F). Due to the night-time temperature drop, relative air humidity increases significantly, rising from 65 to 75% to over 95%. Vegetation at this height is very stunted and slow-growing due to the extreme environmental conditions that prevail. Plants are often subjected to fierce winds and driving rain, as well as exposure to intense direct sunlight. The relatively open vegetation of the upper montane forest also experiences greater fluctuations in temperature and humidity compared with lower altitudes. These changes are largely governed by the extent of cloud cover. In the absence of clouds, temperatures rise rapidly, humidity drops, and light levels may be very high. When cloud cover returns, temperatures and light levels fall, while humidity levels increase.
Conservation status
Endangered species
N. rajah is an Endangered (EN – B1+2e) on the IUCNRed List of Threatened Species. It is listed on Schedule I, Part II of the Wildlife Conservation Enactment (WCE) 1997 and CITES Appendix I, which prohibits commercial international trade in plants collected from the wild. Many plants have been removed from the wild illegally, depleting some populations within Kinabalu Park in the 1970s. This led to the CITES listing in 1981.
The recent advent of artificial tissue culture, or more specifically in vitro, technology in Europe and the United States has meant that plants can be produced in large numbers and sold at relatively low prices (~US$20–$30 in the case of N. rajah). In vitropropagation refers to production of whole plants from cell cultures derived from explants (generally seeds). This technology has largely removed the incentive for collectors to travel to Sabah to collect the plant illegally, and demand for wild-collected plants has fallen. The conservationist Rob Cantley assesses the current status of plants in the wild as due mainly to habitat damage rather than actual theft of plants. The plants in the wild are further threatened by climate phenomena including El Niño; the 1997/98 event and subsequent drought had a catastrophic effect on the Nepenthes on Mount Kinabalu.
Restricted distribution
The Mesilau Nature Resort near the village of Kundasang is now the only place where visitors can hope to see this species in its natural habitat. Daily guided tours are organised. Almost all other populations are in remote parts of Kinabalu National Park, off-limits to tourists.
N. rajah hybridises with all the other Nepenthes species with which it is sympatric. Charles Clarke notes that the pollen of N. rajah can be transported as much as 10 km (6.2 mi).
N. rajah is a montane species or "highlander", growing at altitudes ranging from 1500 to 2650 m. As such, it requires warm days, with temperatures ranging (ideally) from approximately 25 to 30 °C, and cool nights, with temperatures of about 10 to 15 °C. It needs a fairly humid environment to grow well. Values in the region of 75% R.H. have been recommended. In its natural habitat, N. rajah grows in open areas, exposed to direct sunlight. In the tropics, growers can utilise natural sunlight as a source of illumination. In temperate zones, a photoperiod of 12 hours, comparable to that of the tropics, is recommended. The plant produces an extensive root system, requiring a wide pot. The species can tolerate hard water though purified water is recommended by specialists. From trials carried out by a commercial nursery,micronutrient solutions appear to be beneficial. Actual fertilizers (containing NPK) were found to be damaging.
Common misconceptions
Several stories have been told about the species. One such example is the famous legend that N. rajah grows exclusively in the spray zones of waterfalls, on ultramafic soils. Although it is true that they will grow in such places, N. rajah is certainly not found solely in the spray zones of waterfalls. It is likely that the misconception was popularised by Shigeo Kurata's 1976 book Nepenthes of Mount Kinabalu, in which he states that "N. rajah is rather fond of wet places like swamps or the surroundings of a waterfall". Some N. rajah plants do indeed grow near waterfalls (as noted by Hugo Steiner, 2002) "providing quite a humid microclimate". Another myth is that it occasionally catches small monkeys and other large animals in its pitchers. Such tales can probably be explained as rodents being mistaken for other species.
^ Clarke, Charles; Wong, K. M. (1997). Nepenthes of Borneo. Kota Kinabalu: Natural History Publications in association with Science and Technology Unit, Sabah. ISBN983-812-015-4.
^ Wells, K., M.B. Lakim, S. Schulz & M. Ayasse 2011. Pitchers of Nepenthes rajah collect faecal droppings from both diurnal and nocturnal small mammals and emit fruity odour. Journal of Tropical Ecology27(4): 347–353. doi:10.1017/S0266467411000162
^Chin, L., J.A. Moran & C. Clarke 2010. Trap geometry in three giant montane pitcher plant species from Borneo is a function of tree shrew body size. New Phytologist186 (2): 461–470. doi:10.1111/j.1469-8137.2009.03166.x
^Clarke, C., J.A. Moran & L. Chin 2010. Mutualism between tree shrews and pitcher plants: perspectives and avenues for future research. Plant Signaling & Behavior5(10): 1187–1189. doi:10.4161/psb.5.10.12807
^Clarke, C. & J.A. Moran 2011. Incorporating ecological context: a revised protocol for the preservation of Nepenthes pitcher plant specimens (Nepenthaceae). Blumea56(3): 225–228. doi:10.3767/000651911X605781
^ Moran, J.A., C. Clarke, M. Greenwood & L. Chin 2012. Tuning of color contrast signals to visual sensitivity maxima of tree shrews by three Bornean highland Nepenthes species. Plant Signaling & Behavior7(10): 1267–1270. doi:10.4161/psb.21661
^ Greenwood, M., C. Clarke, C.C. Lee, A. Gunsalam & R.H. Clarke 2011. A unique resource mutualism between the giant Bornean pitcher plant, Nepenthes rajah, and members of a small mammal community. PLoS ONE6(6): e21114. doi:10.1371/journal.pone.0021114
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