Nepenthes benstonei
From Wikipedia, the free encyclopedia
| Nepenthes benstonei | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
 Upper pitchers of Nepenthes benstonei
from Bukit Bakar |
||||||||||||||
| Scientific classification | ||||||||||||||
|
||||||||||||||
| Binomial name | ||||||||||||||
| Nepenthes benstonei C.Clarke (1999) |
||||||||||||||
| Synonyms | ||||||||||||||
|
Nepenthes benstonei (pronounced /nəˈpɛnθiːz bɛnˈstəʊniːaɪ/) is a tropical pitcher plant endemic to Peninsular Malaysia, where it occurs at elevations of 450 to 600 m above sea level. The specific epithet benstonei honours botanist Benjamin C. Stone, who was one of the first to collect the species.[1]
Contents |
[edit] Botanical history
In their 1997 monograph "A Skeletal Revision of Nepenthes (Nepenthaceae)", Matthew Jebb and Martin Cheek tentatively referred specimens collected from Bukit Bakar, near Macang, Kelantan to N. sanguinea. These were Stone & Chin 15238, deposited at Universiti Kebangsaan Malaysia near Kuala Lumpur, and Shah & Shukor 3168, also held at the university as well as the Forest Research Institute of Malaysia in Kepong. They noted that the plants exhibited some unusual morphological features, such as larger leaves and decurrent, almost petiolate leaf bases, suggesting that they might represent an as-yet undescribed taxon.[2]
Field studies confirmed that the taxon represented a separate species. It was described as N. benstonei in 1999 by Charles Clarke.[1]
The holotype of N. benstonei, Clarke s.n., was collected by Charles Clarke on July 24, 1998, on Bukit Bakar in Kelantan at an altitude of between 450 and 550 m. It is deposited at the Forest Research Institute of Malaysia in Kepong. Isotypes are held at the Bogor Botanical Gardens, the Royal Botanic Gardens, Kew, the National Herbarium of the Netherlands in Leiden, the Forest Department in Sandakan, and the Singapore Botanic Gardens.[3]
[edit] Ridley 16097
Although only described towards the very end of the twentieth century, N. benstonei was probably first collected in July 1911 by Henry Nicholas Ridley on Mount Tahan in Pahang. The specimen, Ridley 16097, includes female floral material and is deposited at the herbarium of the Singapore Botanic Gardens.[4]
In his seminal monograph "The Nepenthaceae of the Netherlands Indies", B. H. Danser referred Ridley 16097 to N. alata.[4] N. alata was not known from Borneo and this specimen constituted the sole record of N. alata from Peninsular Malaysia. Danser also treated N. eustachya from Sumatra in synonymy with N. alata, making its extreme rarity in Peninsular Malaysia difficult to explain.[3]
In 1990, Ruth Kiew identified Ridley 16097 as belonging to N. gracillima. Kiew explained the apparent near-absence of N. alata from Peninsular Malaysia as follows:[5]
Why has this species not been recollected since 1911 in spite of several botanical expeditions to G. Tahan since then? The answer is quite simple, Ridley's specimen (16097) actually belongs to N. gracillima. Although N. alata Blanco is superficially similar to N. gracillima in its narrow leaf blade which has an attenuate base, the pitchers of these two species are distinct. Those of N. alata are broader (about 4 cm wide) and are distinctly bulbous towards the base compared with the very slender, non-bulbous pitchers of N. gracillima that are 1.5 to 3 cm wide. Nor does the G. Tahan specimen have truly petiolate leaves - its leaf base is narrow and has rolled up during drying. Ridley's specimen from G. Tahan determined by Danser as N. alata bears pitchers typical of N. gracillima and examination of the Tahan population in the field leaves no doubt that it belongs to this species.
Jebb and Cheek supported this interpretation in their monograph.[2]
However, Charles Clarke disagrees with Kiew's identification. He notes that the inflorescences of both N. gracillima and the closely related N. ramispina are very short, rarely exceeding 10 and 20 cm, respectively. Both female inflorescences of Ridley 16097 have a long peduncle and rachis, each exceeding 20 cm in length. In addition, the flowers of these species are almost always borne on pedicels, unlike those of Ridley 16097, which mostly have two-flowered partial peduncles.[6] Furthermore, the shape of the lamina is unlike that of N. gracillima or N. ramispina; despite being narrow and lanceolate, it is proportionately considerably longer and has a much narrower, almost sub-petiolate base. Kiew noted that the lamina of Ridley 16097 appears narrower due to the way in which the specimen was preserved, but Clarke states that this cannot fully account for the differences. He also notes that the specimen exhibits a decurrent leaf attachment. Taking all of these morphological features into account, Clarke feels that Ridley 16097 most likely represents N. benstonei. Clarke considers that Kiew grouped both N. benstonei and N. ramispina with N. gracillima.[3]
[edit] Other specimens
A number of specimens collected from Terengganu also belong to N. benstonei. These are Shah et al. 3274, which is deposited at the Forest Research Institute of Malaysia in Kepong, and Shah et al. 3283, held at the Universiti Kebangsaan Malaysia near Kuala Lumpur.[3][7]
[edit] Description
N. benstonei is a climbing plant. The stem can attain a length of 5 m and is up to 0.6 cm in diameter. Internodes are cylindrical and up to 15 cm long.[3]
Leaves are coriaceous and sessile to sub-petiolate. The lamina is usually broadly linear-lanceolate in shape, but may also be slightly spathulate. Its base is a broad, amplexicaul sheath with decurrent margins. The lamina can reach 60 cm in length and 9 cm in width. It has a rounded to acute apex. The margins of the lamina usually meet the tendril unequally on both sides, being up to 3 mm apart. Three to five longitudinal veins are present on either side of the midrib. Pinnate veins are almost indistinct. Tendrils are up to 60 cm long.[3]
Rosette and lower pitchers reach 20 cm in height[7] and 5 cm in width. They are ovoid in the lower part and cylindrical above, with a pronounced hip in the middle. A pair of fringed wings (≤4 mm wide) runs the whole length of the pitcher cup. The pitcher mouth is round to ovate and oblique throughout. The peristome is up to 6 mm wide and bears very small but distinct teeth along its inner margin. The pitcher lid is ovate and lacks appendages. It bears a short but distinct keel and often has a very broad insertion. A simple or bifurcate spur (≤12 mm long) is inserted near the base of the lid.[3]
Upper pitchers are similar in most respects to their lower counterparts. They are up to 20 cm high[7] and 3 cm wide. They are infundibular in the lowermost part, narrowly ovoid in the next part, and cylindrical above. The peristome lacks teeth in upper pitchers. The lid is narrower and has a less obtuse apex. The spur is simple and much smaller, reaching only 5 mm in length.[3]
N. benstonei has a racemose inflorescence. The peduncle is up to 20 cm long and the rachis up to 30 cm long. The first flower is generally borne on a pedicel, sometimes with a simple, lanceolate bracteole (≤1.5 cm long). Subsequent flowers are produced on pedicels or two-flowered partial peduncles, which lack bracteoles. Sepals are ovate and around 4 mm long. Male inflorescences usually bear around twice as many flowers as female ones. N. benstonei is one of the few Nepenthes species known to produce multiple inflorescences concurrently on a single stem. Two to three are usually produced, originating from sequential nodes at the top of the stem. This unusual reproductive habit has also been observed, although much more rarely, in N. ampullaria, N. rigidifolia, and N. sanguinea.[3]
The stem and lamina have a sparse indumentum of simple white hairs. Short, branched reddish-brown hairs line the margins of the lamina. The outer surfaces of the pitchers bear a sparse covering of short, branched red hairs. The same hairs are more densely present on the margins of the lid and upper part of the pitcher directly below the peristome. Immature inflorescences have an indumentum of short white and red hairs throughout.[3]
The stem and leaves of N. benstonei bear a thick, waxy cuticle that often gives a whitish-blue sheen to the lamina and pitchers. Inflorescences are distinctly waxy throughout.[3]
No infraspecific taxa of N. benstonei have been described.[3]
[edit] Ecology
N. benstonei is endemic to Peninsular Malaysia. It is known with certainty only from the summits of low hills in Kelantan and northern Terengganu, although collections and observations from Pahang and Taman Negara National Park suggest it may be more widespread in the region.[3][7]
N. benstonei grows terrestrially amongst open, secondary vegetation, where it is exposed to direct sunlight. It is very abundant near the summit of Bukit Bakar, where it grows on cuttings beside a paved road leading to a Telekom Malaysia station at the summit. The exact boundaries of its altitudinal distribution are not yet known, but it has been recorded from elevations of 450 to 600 m above sea level.[3][7]
Although the extent of its range is uncertain, N. benstonei appears to have a secure future in the wild as the type locality lies within a protected area and the species's unremarkable appearance means over-collection does not pose a serious threat.[3]
[edit] Related species
In his description of N. benstonei, Charles Clarke noted two characteristics that he considered unique among Nepenthes. These were the production of multiple inflorescences and the presence of a thick, waxy cuticle on the leaves.[1] However, subsequent field studies have shown that the former is not unique to N. benstonei, but also occasionally occurs in other Nepenthes. Likewise, a number of other species, such as N. hirsuta from Borneo, are known to produce a waxy cuticle, although it is less developed than in N. benstonei.[3] Otherwise, N. benstonei lacks remarkable characteristics and is distinguished from related species on the basis of its stem, leaves, peristome, lid, indumentum, and glands of the digestive zone.[1]
N. benstonei appears to be related to N. sanguinea, which is also endemic to Peninsular Malaysia. It can be distinguished on the basis of its significantly larger leaves, which are often sub-petiolate and differ in shape. N. benstonei also has longer tendrils and a denser indumentum. The presence of teeth on the peristome of lower pitchers and of a thick, waxy cuticle on the leaves also serve to distinguish these taxa. In addition, herbarium specimens of N. benstonei tend to dry to a lighter colour than those of N. sanguinea.[3]
The pitchers of N. benstonei also resemble those of N. anamensis from Indochina. Clarke suggests that N. benstonei may represent an evolutionary link between the Nepenthes taxa of Indochina and Peninsular Malaysia.[7]
N. benstonei also superficially resembles N. macrovulgaris from Borneo. It differs in producing multiple inflorescences, which are longer than those of N. macrovulgaris and bear one- or two-flowered partial peduncles, as opposed to exclusively two-flowered in the latter. The waxy coating of its leaves also separates these species.[3]
N. benstonei has also been compared to N. albomarginata, although the presence of a white band below the peristome, which gives the latter its name, makes identification easy.[3]
.jpg/180px-Apes_abroad_-_Jug_Plant_(by-sa).jpg)
Upper pitchers of N. benstonei could be confused with those of N. mirabilis, although all other parts of the plant have little in common.[3]
In 2001, Charles Clarke performed a cladistic analysis of the Nepenthes species of Sumatra and Peninsular Malaysia using 70 morphological characteristics of each taxon. The resultant cladogram placed N. benstonei in an unresolved polytomy at the base of the Montanae/Nobiles clade, together with N. rhombicaulis.[3]
[edit] Natural hybrids
Only one natural hybrid involving N. benstonei is known. A single example of N. benstonei × N. mirabilis was discovered by Andrew Hurrell at the foot of Bukit Bakar, where the two species occur sympatrically.[3][7]
[edit] References
- ^ a b c d Clarke, C.M. 1999. Nepenthes benstonei (Nepenthaceae), a new pitcher plant from Peninsular Malaysia. Sandakania 13: 79–87.
- ^ a b Jebb, M.H.P. & M.R. Cheek 1997. A Skeletal Revision of Nepenthes (Nepenthaceae). Blumea 42(1): 1–106.
- ^ a b c d e f g h i j k l m n o p q r s t u v Clarke, C.M. 2001. Nepenthes of Sumatra and Peninsular Malaysia. Natural History Publications (Borneo), Kota Kinabalu.
- ^ a b Danser, B.H. 1928. The Nepenthaceae of the Netherlands Indies. Bulletin de Jardin de Botanique, Buitenzorg, Série III, 9(3–4): 249–438.
- ^ Kiew, R.G. 1990. Pitcher plants of Gunung Tahan. Journal of Wildlife and National Parks (Malaysia) 10: 34–37.
- ^ Shivas, R.G. 1984. Pitcher plants of Peninsular Malaysia and Singapore. Maruzen Asia, Kuala Lumpur.
- ^ a b c d e f g Clarke, C.M. 2002. A Guide to the Pitcher Plants of Peninsular Malaysia. Natural History Publications (Borneo), Kota Kinabalu.
[edit] External links
Miscellaneous: Nepenthes taxonomy • Nepenthes infauna
