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Biology

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Pitcher plants are dioecious, meaning that male and female flowers grow on separate plants (4), and only begin to flower once the upper pitchers are produced (5). The flowers produce large amounts of nectar during the early evening and night, which evaporates by morning. This nectar attracts flies during the early evening and moths at night to aid pollination. Once fertilised, a fruit usually takes about three months to develop and ripen. The fruits of Nepenthes species produce between 100 and 500 very light, winged seeds, which can measure up to 30 millimetres long, and are thought to be dispersed by the wind (2) (6). Despite enormous numbers of seeds being produced, only a few manage to germinate and only a fraction of those survive to maturity (2). Carnivorous pitcher plants are adapted to grow in soils low in nutrients. Although the plants do gain some nutrition through the soil, and energy through photosynthesis, they supplement this with a diet of invertebrates, usually consisting of ants, cockroaches, centipedes, flies and beetles (4). Insects are attracted to the pitchers by their bright colours and nectar, which is secreted by glands situated on the lid and the peristome of the pitcher. The insects fall into the acidic fluid at the base of the pitcher and are unable to escape. Digestive enzymes are then released to break down the drowned prey (4). Despite the hostile environment of the pitchers, they can be home to number of animals. The red crab spider (Misumenops nepenthicola) inhabits pitcher plants in Malaysia, Indonesia and Singapore. This spider ambushes insects that crawl into the pitcher and preys upon other insects, such as mosquitoes, as they emerge from larvae that live in the pitcher fluid (2).
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Conservation

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Most populations of Nepenthes faizaliana grow in remote and inaccessible areas within Gunung Mulu National Park, reducing the threat from collectors (2) (8). It is also listed under Appendix II of the Convention on International Trade in Endangered Species (CITES) which limits the international export of this species (3). However, trade is very difficult to regulate and there is no requirement for internationally traded Nepenthes to be identified down to species level. Plants simply labelled as Nepenthes accounted for 94 percent of all exported Nepenthes plants between 1988 and 1993. This needs to be remedied and urgent attention is required to close other trade loopholes (2). Nepenthes species, including Nepenthes faizaliana, are being increasingly cultivated, helping to reduce the impact on wild populations. Artificial propagation can help make conservation efforts more effective together with the establishment of more habitat reserves and the implementation and enforcement of protective laws (9).
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Description

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This spectacular carnivorous plant is a vine, from which modified pitcher-shaped leaves hang from coiled tendrils and into which insects and other invertebrates fall (2) (4). The pitchers are narrowly trumpet-shaped, gradually widening towards the mouth, and are green with red-brown blotches (2). The pitchers contain an acidic fluid, secreted by the many glands which cover the inside surface of the pitcher (2). The peristome, a ridge of hardened tissue lining the mouth of the pitcher, bears downward pointing teeth, also preventing insects from escaping (2). A lid overhangs the mouth of the pitcher and prevents rain water from diluting the pitcher fluid (2). White hairs cover the stem and the underside of the leaves (2).
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Habitat

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Nepenthes faizaliana grows on limestone outcrops on wet, sandy soils. It is abundant in open areas or on ridge tops, growing either terrestrially or as an epiphyte (2).
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Range

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Endemic to Sarawak, in the Indonesian region of Borneo, where it is found only in Gunung Mulu National Park between 1,000 and 2,600 metres above sea level (2).
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Status

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Classified as Vulnerable (VU) on the IUCN Red List (1) and listed on Appendix II of CITES (3).
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Threats

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Nepenthes species are threatened by a combination of over-collection and habitat loss (2). The biodiversity of Indonesia is significantly threatened by widespread habitat destruction, caused by illegal and commercial logging and large agricultural projects such as rubber and oil palm plantations (7). Nepenthes faizaliana has a highly localised distribution making this species particularly susceptible to extinction from habitat destruction and catastrophic environmental events, such as drought or fire. In addition, montane species, such as Nepenthes faizaliana, take longer to recover than lowland plants after such events, as growth is slower (2).
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Nepenthes faizaliana

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Nepenthes faizaliana /nɪˈpɛnθz ˌfzæliˈɑːnə/ is a tropical pitcher plant endemic to the limestone cliffs of Gunung Mulu National Park in Sarawak, Borneo. It is thought to be most closely related to N. boschiana.[3]

Botanical history

The type specimen of N. faizaliana, S 44163 (Lai & Jugah), was collected on November 10, 1981, on Batu Panjang[4] in Gunung Mulu National Park.[5] The holotype is deposited at the Sarawak Forest Department Herbarium (SAR) in Kuching, Sarawak; isotypes are held at the herbarium of the Royal Botanic Gardens, Kew (K) and at the National Herbarium of the Netherlands (L) in Leiden.[5]

Nepenthes faizaliana was formally described in 1991 by J. H. Adam and C. C. Wilcock. The description was published in the botanical journal Blumea.[2] Nepenthes faizaliana was named after Muhammad Khairul Faizal, son of describing author J. H. Adam.[2]

In 1997, Matthew Jebb and Martin Cheek reduced N. faizaliana to a heterotypic synonym of N. stenophylla in their monograph on the genus.[6] This treatment was followed by Anthea Phillipps and Anthony Lamb in their book Pitcher-Plants of Borneo.[7] However, Charles Clarke retained N. faizaliana as a distinct species in his monograph Nepenthes of Borneo, which was published a few months after the work of Jebb and Cheek.[3] This interpretation has been supported by subsequent authors.[4][5][8][9]

Description

The climbing stem of Nepenthes faizaliana may be up to 8 mm in diameter. Internodes are cylindrical in cross section and up to 3 cm long.[3]

A lower pitcher

The leaves alternate around the stem. They are petiolate and coriaceous in texture. The lamina is lanceolate to elliptic in shape and up to 14 cm long by 4 cm wide. It has an acute apex and an obtuse base. The petiole is canaliculate and up to 5 cm long. It is semi-amplexicaul, but lacks wings. Two longitudinal veins are present on either side of the midrib. Pinnate veins are indistinct. Tendrils reach 20 cm in length.[3]

Lower pitchers have not been formally described,[3] although they are smaller and less frequently produced than their aerial counterparts.[10] Upper pitchers are narrowly infundibular, becoming slightly wider in the upper part. They reach over 30 cm in height.[10] In aerial pitchers, wings are usually reduced to a pair of ribs.[3] The waxy zone of the inner surface is well developed.[11] The pitcher mouth has an oblique insertion. The peristome is flattened, cylindrical in cross section, and up to 4 mm wide. The lid or operculum is orbicular and has a distinctive glandular crest on its underside. An unbranched spur is inserted near the base of the lid.[3]

An intermediate pitcher

Nepenthes faizaliana has a racemose inflorescence. The female inflorescence of this species has not been formally described.[3] In male inflorescences, the peduncle is up to 17 cm long, while the axis reaches 40 cm in length. Pedicels are one-flowered, up to 20 mm long, and typically possess bracts. Sepals are lanceolate to oblong in shape and up to 4 mm long.[3] A study of 120 pollen samples taken from the type specimen (S 44163 (Lai & Jugah)) found the mean pollen diameter to be 32.3 μm (SE = 0.4; CV = 7.6%).[12]

Nepenthes faizaliana bears an indumentum of white, stellate hairs on its stem and petioles. The upper surface of the lamina is glabrous, whereas the underside has a sparse covering of short, branched hairs. In addition, long white hairs are present at the base of the midrib.[3]

Ecology

Nepenthes faizaliana is endemic to the limestone peaks of Gunung Mulu National Park in Sarawak, Borneo.[3] It typically occurs at elevations of 1000 to 1600 m above sea level,[3][9] although it has been recorded from elevations as low as 400 m.[10] N. faizaliana occurs both terrestrially and as an epiphyte on limestone outcrops and exposed ridge tops.[10] It grows in close proximity to a number of other Nepenthes species, including N. stenophylla, N. tentaculata, and N. vogelii, but only one putative natural hybrid with N. veitchii has been recorded.[8]

Nepenthes faizaliana growing along the Pinnacles Trail on Mount Api

Although most populations of N. faizaliana are remote and inaccessible to regular visitors, the species can be easily observed along the Pinnacles Trail on Mount Api.[10][13]

Related species

Nepenthes faizaliana belongs to the loosely defined "N. maxima complex", which also includes, among other species, N. boschiana, N. chaniana, N. epiphytica, N. eymae, N. fusca, N. klossii, N. maxima, N. platychila, N. stenophylla, and N. vogelii.[14]

Nepenthes faizaliana appears to be most closely related to N. boschiana. These two species differ in the extent of their indumentums; that of N. faizaliana is well developed and conspicuous, while mature plants of N. boschiana are virtually glabrous. In addition, the lower pitchers of N. boschiana tend to have a more bulbous base and a wider peristome. The upper pitchers are hard to distinguish, although those of N. boschiana usually have a wider mouth. Charles Clarke writes that these differences are "not major" and that "closer comparisons seem warranted".[3] Nepenthes boschiana and N. faizaliana are both limestone endemics and occur on the highest limestone formations in Borneo: the Meratus Range and the cliffs of Gunung Mulu National Park, respectively.[3]

An upper pitcher of N. faizaliana (left) and N. stenophylla (right)

Nepenthes faizaliana is also similar to N. stenophylla, with which it was once synonymised. It differs from that species in having more lanceolate leaves, larger inflorescences, as well as a wider, more colourful[10] and less recurved peristome. The flowers of N. faizaliana are borne singly on bracteate pedicels rather than on two-flowered partial peduncles. In addition, the glandular crest of N. faizaliana differs in shape and its lower pitchers are generally bulbous in the lower parts, unlike those of N. stenophylla.[3] Some authors treat N. fallax in synonymy with N. stenophylla, while others consider them to be two distinct species, with plants commonly referred to as N. stenophylla actually representing N. fallax.[3][15][16]

Nepenthes faizaliana also bears a resemblance to N. fusca. In their description of the former, Adam and Wilcock distinguished these taxa on the basis of inflorescence structure, the size of the glandular region on the inner surface of upper pitchers, and the development and characteristics of the indumentum.[2][3] In addition, N. faizaliana differs in having an orbicular pitcher lid, as opposed to the very narrow lid of N. fusca.[3]

References

  1. ^ Clarke, C.M. (2018). "Nepenthes faizaliana". IUCN Red List of Threatened Species. 2018: e.T40108A143966870. doi:10.2305/IUCN.UK.2018-1.RLTS.T40108A143966870.en. Retrieved 19 November 2021.
  2. ^ a b c d Adam, J.H. & C.C. Wilcock 1991. A new species of Nepenthes (Nepenthaceae) from Sarawak. Blumea 36(1): 123–125.
  3. ^ a b c d e f g h i j k l m n o p q r Clarke, C.M. 1997. Nepenthes of Borneo. Natural History Publications (Borneo), Kota Kinabalu.
  4. ^ a b Schlauer, J. N.d. Nepenthes faizaliana. Carnivorous Plant Database.
  5. ^ a b c Cheek, M.R. & M.H.P. Jebb 2001. Nepenthaceae. Flora Malesiana 15: 1–157.
  6. ^ Jebb, M.H.P. & M.R. Cheek 1997. A skeletal revision of Nepenthes (Nepenthaceae). Blumea 42(1): 1–106.
  7. ^ Phillipps, A. & A. Lamb 1996. Pitcher-Plants of Borneo. Natural History Publications (Borneo), Kota Kinabalu.
  8. ^ a b Phillipps, A., A. Lamb & C.C. Lee 2008. Pitcher Plants of Borneo. Second Edition. Natural History Publications (Borneo), Kota Kinabalu.
  9. ^ a b McPherson, S.R. 2009. Pitcher Plants of the Old World. 2 volumes. Redfern Natural History Productions, Poole.
  10. ^ a b c d e f Clarke, C.M. & C.C. Lee 2004. Pitcher Plants of Sarawak. Natural History Publications (Borneo), Kota Kinabalu.
  11. ^ Bauer, 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 Biology 25(1): 90–102. doi:10.1111/j.1420-9101.2011.02406.x
  12. ^ Adam, J.H. & C.C. Wilcock 1999. Palynological study of Bornean Nepenthes (Nepenthaceae). Pertanika Journal of Tropical Agricultural Science 22(1): 1–7.
  13. ^ Steiner, H. 2002. Borneo: Its Mountains and Lowlands with their Pitcher Plants. Toihaan Publishing Company, Kota Kinabalu.
  14. ^ Robinson, A.S., J. Nerz & A. Wistuba 2011. Nepenthes epiphytica, a new pitcher plant from East Kalimantan. In: McPherson, S.R. New Nepenthes: Volume One. Redfern Natural History Productions, Poole. pp. 36–51.
  15. ^ Schlauer, J. 2006. Nepenthes fallax. Carnivorous Plant Database.
  16. ^ Schlauer, J. 1996. N.stenophylla, once again. Carnivorous Plant Mailing List, May 31, 1996.
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Nepenthes faizaliana: Brief Summary

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Nepenthes faizaliana /nɪˈpɛnθiːz ˌfaɪzæliˈɑːnə/ is a tropical pitcher plant endemic to the limestone cliffs of Gunung Mulu National Park in Sarawak, Borneo. It is thought to be most closely related to N. boschiana.

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