Nepenthes faizaliana | |
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An upper pitcher of Nepenthes faizaliana from Mount Api | |
Scientific classification ![]() | |
Kingdom: | Plantae |
Clade: | Tracheophytes |
Clade: | Angiosperms |
Clade: | Eudicots |
Order: | Caryophyllales |
Family: | Nepenthaceae |
Genus: | Nepenthes |
Species: | N. faizaliana
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Binomial name | |
Nepenthes faizaliana |
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.[3]
Botanical history
[edit]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
[edit]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]
![](https://upload.wikimedia.org/wikipedia/commons/thumb/1/1f/Pinnacles_N._faizaliana_10.jpg/160px-Pinnacles_N._faizaliana_10.jpg)
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]
![](https://upload.wikimedia.org/wikipedia/commons/thumb/4/42/Pinnacles_N._faizaliana_16.jpg/220px-Pinnacles_N._faizaliana_16.jpg)
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
[edit]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]
![](https://upload.wikimedia.org/wikipedia/commons/thumb/7/74/Pinnacles_N._faizaliana_14.jpg/220px-Pinnacles_N._faizaliana_14.jpg)
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
[edit]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]
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
[edit]- ^ 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.
- ^ a b c d Adam, J.H. & C.C. Wilcock 1991. A new species of Nepenthes (Nepenthaceae) from Sarawak. Blumea 36(1): 123–125.
- ^ 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.
- ^ a b Schlauer, J. N.d. Nepenthes faizaliana. Carnivorous Plant Database.
- ^ a b c Cheek, M.R. & M.H.P. Jebb 2001. Nepenthaceae. Flora Malesiana 15: 1–157.
- ^ Jebb, M.H.P. & M.R. Cheek 1997. A skeletal revision of Nepenthes (Nepenthaceae). Blumea 42(1): 1–106.
- ^ Phillipps, A. & A. Lamb 1996. Pitcher-Plants of Borneo. Natural History Publications (Borneo), Kota Kinabalu.
- ^ a b Phillipps, A., A. Lamb & C.C. Lee 2008. Pitcher Plants of Borneo. Second Edition. Natural History Publications (Borneo), Kota Kinabalu.
- ^ a b McPherson, S.R. 2009. Pitcher Plants of the Old World. 2 volumes. Redfern Natural History Productions, Poole.
- ^ a b c d e f Clarke, C.M. & C.C. Lee 2004. Pitcher Plants of Sarawak. Natural History Publications (Borneo), Kota Kinabalu.
- ^ 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
- ^ Adam, J.H. & C.C. Wilcock 1999. Palynological study of Bornean Nepenthes (Nepenthaceae). Pertanika Journal of Tropical Agricultural Science 22(1): 1–7.
- ^ Steiner, H. 2002. Borneo: Its Mountains and Lowlands with their Pitcher Plants. Toihaan Publishing Company, Kota Kinabalu.
- ^ 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.
- ^ Schlauer, J. 2006. Nepenthes fallax Archived 2020-05-13 at the Wayback Machine. Carnivorous Plant Database.
- ^ Schlauer, J. 1996. N.stenophylla, once again. Carnivorous Plant Mailing List, May 31, 1996.
Further reading
[edit]- Bourke, G. 2011. The Nepenthes of Mulu National Park. Carniflora Australis 8(1): 20–31.
- Lee, C.C. 2000. Recent Nepenthes Discoveries. [video] The 3rd Conference of the International Carnivorous Plant Society, San Francisco, USA.
- McPherson, S.R. & A. Robinson 2012. Field Guide to the Pitcher Plants of Borneo. Redfern Natural History Productions, Poole.
- Meimberg, H., A. Wistuba, P. Dittrich & G. Heubl 2001. Molecular phylogeny of Nepenthaceae based on cladistic analysis of plastid trnK intron sequence data. Plant Biology 3(2): 164–175. doi:10.1055/s-2001-12897
- (in German) Meimberg, H. 2002. Molekular-systematische Untersuchungen an den Familien Nepenthaceae und Ancistrocladaceae sowie verwandter Taxa aus der Unterklasse Caryophyllidae s. l.. Ph.D. thesis, Ludwig Maximilian University of Munich, Munich.
- Meimberg, H. & G. Heubl 2006. Introduction of a nuclear marker for phylogenetic analysis of Nepenthaceae. Plant Biology 8(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 Evolution 39(2): 478–490. doi:10.1016/j.ympev.2005.11.023
- Mey, F.S. 2014. Joined lecture on carnivorous plants of Borneo with Stewart McPherson. Strange Fruits: A Garden's Chronicle, February 21, 2014.
- Thorogood, C. 2010. The Malaysian Nepenthes: Evolutionary and Taxonomic Perspectives. Nova Science Publishers, New York.