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Nepenthes ampullaria

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Nepenthes ampullaria
Rosette pitcher of Nepenthes ampullaria from Bako National Park, Borneo
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Order: Caryophyllales
Family: Nepenthaceae
Genus: Nepenthes
Species:
N. ampullaria
Binomial name
Nepenthes ampullaria
Jack (1835)
Synonyms

Nepenthes ampullaria (/nɪˈpɛnθiːz ˌæmpʊˈlɛəriə/; Latin ampulla meaning "flask") is a very distinctive and widespread species of tropical pitcher plant, present in Borneo, the Maluku Islands, New Guinea, Peninsular Malaysia, Singapore, Sumatra, and Thailand.[2][3][4][5][6]

Nepenthes ampullaria, unlike other members of its genus, has evolved away from carnivory and the plants are partly detritivores, collecting and digesting falling leaf litter in their pitchers.[7][8][9]

In the 1996 book Pitcher-Plants of Borneo, N. ampullaria is given the vernacular name flask-shaped pitcher-plant.[10] This name, along with all others, was dropped from the much-expanded second edition, published in 2008.[11]

Description

N. ampullaria with climbing stems and rosette pitchers.

Due to its unique pitcher morphology and unusual growth habit, it is difficult to confuse N. ampullaria with any other species in the genus. Francis Ernest Lloyd translated Troll's 1932 account of this species as follows:[12]

"I came across N. ampullaria among the massive vegetations of a swamp-forest on the island of Siberut off the west coast of Sumatra. It was a fabulous, unforgettable sight. Everywhere, through the network of lianas the peculiarly-formed pitchers of this species gleamed forth, often in tight clusters and, most remarkably, the muddy moss-overgrown soil was spotted with the pitchers of this plant, so that one got the impression of a carpet."

The stem of N. ampullaria is light brown in colour and may climb to 15 m in height. Leaves are light green, up to 25 cm long, and 6 cm wide. Pitchers are produced at the ends of short tendrils no more than 15 cm long.[13]

The urceolate pitchers are generally quite small, rarely exceeding 10 cm in height and 7 cm in width. The peristome is greatly incurved, with the inner section accounting for around 85% of its total cross-sectional surface length.[14] Upper pitchers are very rarely produced and are considerably smaller than those formed on rosettes or offshoots. Pitchers range in colouration from light green throughout to completely dark red, with many intermediate forms recorded. The pitchers of N. ampullaria from Sumatra and Peninsular Malaysia are almost exclusively green throughout or green with red speckles; the red forms are mostly confined to Borneo. A large-pitchered form has been recorded from New Guinea.[13][15]

Nepenthes ampullaria at the Bogor Botanical Gardens

The inflorescence of N. ampullaria is a dense panicle. It is the only Nepenthes species recorded from Sumatra or Peninsular Malaysia that produces paniculate inflorescences.[15]

All parts of the plant are densely covered with short, brown hairs when young. The indumentum of mature plants is more sparse, except on the inflorescenes.[13]

Distribution and habitat

One of the most widespread Nepenthes species, N. ampullaria is native to Borneo, the Maluku Islands, New Guinea, Peninsular Malaysia, Singapore, Sumatra, and Thailand.[2] It has also been recorded from many smaller islands, including Bangka, Bengkalis, Ko Lanta, Ko Tarutao, Langkawi, Mendol, the Mentawai Islands (Siberut), the Meranti Islands (Padang, Rangsang, Tebing Tinggi), Nias, Penang, the Riau Islands (Lingga Islands, Natuna Islands,[16] Riau Archipelago), and Rupat.[17]

Nepenthes ampullaria generally grows in damp, shady forest from sea-level to 2100 m altitude.[18] In Borneo, it occurs usually on relatively flat terrain in kerangas forest, peat swamp forest, and degraded swamp forest, at elevations of 0 to 1000 m.[13]

In Sumatra and Peninsular Malaysia, it grows from sea-level to 1100 m altitude on flat terrain in heath forest, padang (meaning "field" in Malay), belukar, peat swamp forest, degraded swamp forest, and in padi fields.[15]

In New Guinea, it is predominantly present in Araucaria forests. The species has also been recorded from secondary forests, open microphyllous vegetation, and swamp grassland.[18]

Carnivory

See also: Protocarnivorous plant
N. ampullaria is well-adapted to capturing leaf litter.

Nepenthes ampullaria has largely moved away from carnivory and acquires a substantial portion of its nutrients from digesting leaf matter that falls to the forest floor. It is thus partially detritivorous.

The species has developed several unique traits as a consequence of its adaptation to trapping leaf litter:[15]

  • It is one of the few species in the genus to lack "lunate" cells in its pitchers.[19][20] These are modified stomatal guard cells which, it is thought, deny prey a foothold in the pitcher.[12]
  • The pitcher lid is atypical, being very small and reflexed, such that leaf litter is allowed to fall directly into the pitcher.[15]
  • Nectar glands, which play an important role in prey capture, are very rare and in some cases completely absent from the pitcher lid.[15]
  • The marginal glands of the peristome are greatly reduced compared to those of other species.[15]
  • In terrestrial pitchers, the glandular region extends almost to the peristome, such that there is little or no conductive waxy zone.[13][20][21][22][23] The waxy zone functions by causing prey to slip and fall into the digestive fluid.[15]
  • The plant's architecture, consisting of subsurface runners and offshoots, is unusual for the genus. The species often forms a "carpet" of pitchers covering the soil. This serves to maximise the area over which falling debris may be intercepted.[15]
  • The pitchers of N. ampullaria are relatively long-lived, as the species relies on a slow accumulation of nutrients over time.[15]
  • It is thought that infaunal organisms, such as mosquito larvae, facilitate breakdown of leaf litter and aid in the transfer of nitrogen from it to the plant by means of the excretion of ammonium ions. Bacterial breakdown of leaf matter is also known to produce ammonium ions.[15]

It has been shown that foliar stable nitrogen isotope (15N) abundance in N. ampullaria plants growing under forest canopy (litterfall present) is significantly lower than in plants without access to litterfall. Conversely, total nitrogen concentrations are higher in these plants compared to those growing in open sites with no litterfall. A 2003 study estimated that N. ampullaria plants growing under forest canopy derive 35.7% (±0.1%) of their foliar nitrogen from leaf litter.[7] A 2011 study found that N. ampullaria derives 41.7% (±5.5%) of its laminar nitrogen and 54.8% (±7.0%) of its pitcher nitrogen from leaf litter, and showed that detritivory increased the rate of net photosynthesis in the laminae.[8]

Pitcher infauna

At least 59 infaunal species have been recorded from the pitchers of N. ampullaria.[24] Among these are one of the smallest known species of Old World frog, Microhyla nepenthicola, and the crab spider "Misumenops nepenthicola" (properly one or more species of Henriksenia).[25][26] The bacterial communities found in the pitchers of this species have also been studied.[27]

Infraspecific taxa

A red form of N. ampullaria
A tiny upper pitcher of N. ampullaria from Sumatra. Such aerial traps are commonly or rarely produced depending on the variety and appear almost vestigial, often being too small to catch prey.[15]

The most recently described variety, N. ampullaria var. racemosa, occurs in Sarawak and has a racemose inflorescence. B. H. Danser considered the other varieties to be unimportant.[28] A complete list of published varietal names includes:[29]

  • N. ampullacea var. picta Hort.Parker ex Rafarin (1869)
  • N. ampullacea var. vittata Hort.Van Houtte ex Rafarin (1869)
  • N. ampullaria var. geelvinkiana Becc. (1886)
  • N. ampullaria var. guttata D.Moore (1872)[30]
  • N. ampullaria var. longicarpa Becc. (1886)
  • N. ampullaria var. microsepala Macfarl. (1911)
  • N. ampullaria var. papuana Becc. in sched. nom.nud.
  • N. ampullaria var. racemosa J.H.Adam & Wilcock (1990)
  • N. ampullaria var. viridis Hort. ex Teijsm. (1859)[31] nom.nud.
  • N. ampullaria var. vittata-major Mast. (1872)[32]

Natural hybrids

N. ampullaria flowers once or twice annually for several weeks at a time. Its flowering period often coincides with those of other Nepenthes species; consequently, it readily forms natural hybrids. The following natural hybrids involving N. ampullaria have been recorded.

References

  1. ^ Clarke, C.M. (2018). "Nepenthes ampullaria". IUCN Red List of Threatened Species. 2018: e.T39640A143958546. doi:10.2305/IUCN.UK.2018-1.RLTS.T39640A143958546.en. Retrieved 19 November 2021.
  2. ^ a b c d McPherson, S.R. 2009. Pitcher Plants of the Old World. 2 volumes. Redfern Natural History Productions, Poole.
  3. ^ (in Italian) Catalano, M. 2010. Nepenthes della Thailandia: Diario di viaggio. Prague.
  4. ^ McPherson, S.R. & A. Robinson 2012. Field Guide to the Pitcher Plants of Peninsular Malaysia and Indochina. Redfern Natural History Productions, Poole.
  5. ^ McPherson, S.R. & A. Robinson 2012. Field Guide to the Pitcher Plants of Australia and New Guinea. Redfern Natural History Productions, Poole.
  6. ^ McPherson, S.R. & A. Robinson 2012. Field Guide to the Pitcher Plants of Sumatra and Java. Redfern Natural History Productions, Poole.
  7. ^ a b Moran, J.A., C.M. Clarke & B.J. Hawkins 2003. From carnivore to detritivore? Isotopic evidence for leaf litter utilization by the tropical pitcher plant Nepenthes ampullaria. International Journal of Plant Sciences 164(4): 635–639. doi:10.1086/375422
  8. ^ a b Pavlovič, A., Ľ. Slováková & J. Šantrůček 2011. Nutritional benefit from leaf litter utilization in the pitcher plant Nepenthes ampullaria. Plant, Cell & Environment 34(11): 1865–1873. doi:10.1111/j.1365-3040.2011.02382.x
  9. ^ Pavlovič, A. 2012. Adaptive radiation with regard to nutrient sequestration strategies in the carnivorous plants of the genus Nepenthes. Plant Signaling & Behavior 7(2): 295–297. doi:10.4161/psb.18842
  10. ^ Phillipps, A. & A. Lamb 1996. Pitcher-Plants of Borneo. Natural History Publications (Borneo), Kota Kinabalu.
  11. ^ Phillipps, A., A. Lamb & C.C. Lee 2008. Pitcher Plants of Borneo. Second Edition. Natural History Publications (Borneo), Kota Kinabalu.
  12. ^ a b Lloyd, F.E. 1942. The Carnivorous Plants. Chronica Botanica 9. Ronald Press Company, New York, U.S.A. xvi + 352 pp.
  13. ^ a b c d e f g h i j k Clarke, C.M. 1997. Nepenthes of Borneo. Natural History Publications (Borneo), Kota Kinabalu.
  14. ^ 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
  15. ^ a b c d e f g h i j k l m n Clarke, C.M. 2001. Nepenthes of Sumatra and Peninsular Malaysia. Natural History Publications (Borneo), Kota Kinabalu.
  16. ^ (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 21 September 2013 at the Wayback Machine
  17. ^ Clarke, C.M. 2001. Appendix C: Distribution Maps. In: Nepenthes of Sumatra and Peninsular Malaysia. Natural History Publications (Borneo), Kota Kinabalu. pp. 299–307.
  18. ^ a b Jebb, M.H.P. & M.R. Cheek 1997. A skeletal revision of Nepenthes (Nepenthaceae). Blumea 42(1): 1–106.
  19. ^ Pant, D.D. & S. Bhatnagar 1977. Morphological studies in Nepenthes (Nepenthaceae). Phytomorphology 27: 13–34.
  20. ^ a b Moran, J.A., B.J. Hawkins, B.E. Gowen & S.L. Robbins 2010. Ion fluxes across the pitcher walls of three Bornean Nepenthes pitcher plant species: flux rates and gland distribution patterns reflect nitrogen sequestration strategies. Journal of Experimental Botany 61(5): 1365–1374. doi:10.1093/jxb/erq004
  21. ^ Macfarlane, J.M. 1893. Observations on pitchered insectivorous plants. (Part II.). Annals of Botany 7(4): 403–458.
  22. ^ Jebb, M.H.P. 1991. An account of Nepenthes in New Guinea. Science in New Guinea 17(1): 7–54.
  23. ^ Di Giusto, B., M. Guéroult, N. Rowe & L. Gaume 2009. Chapter 7: The Waxy Surface in Nepenthes Pitcher Plants: Variability, Adaptive Significance and Developmental Evolution. In: S.N. Gorb (ed.) Functional Surfaces in Biology: Adhesion Related Phenomena. Volume 2. Springer. pp. 183–204.
  24. ^ Adlassnig, W., M. Peroutka & T. Lendl 2011. Traps of carnivorous pitcher plants as a habitat: composition of the fluid, biodiversity and mutualistic activities. Annals of Botany 107(2): 181–194. doi:10.1093/aob/mcq238
  25. ^ Das, I. & A. Haas. 2010. New species of Microhyla from Sarawak: Old World's smallest frogs crawl out of miniature pitcher plants on Borneo (Amphibia: Anura: Microhylidae). Zootaxa 2571: 37–52.
  26. ^ Gururaja, K.V. 2010. Old World’s smallest frog discovered residing in killer plants. Current Science 99(8): 1000.
  27. ^ Chou, L.Y., C.M. Clarke & G.A. Dykes 2014. Bacterial communities associated with the pitcher fluids of three Nepenthes (Nepenthaceae) pitcher plant species growing in the wild. Archives of Microbiology 196(10): 709–717. doi:10.1007/s00203-014-1011-1
  28. ^ Danser, B.H. 1928. The Nepenthaceae of the Netherlands Indies. Bulletin du Jardin Botanique de Buitenzorg, Série III, 9(3–4): 249–438.
  29. ^ Schlauer, J. N.d. Nepenthes ampullaria. Carnivorous Plant Database.
  30. ^ Moore, D. 1872. On the culture of Nepenthes at Glasnevin. The Gardeners' Chronicle and Agricultural Gazette 1872(11): 359–360.
  31. ^ (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.
  32. ^ Masters, M.T. 1872. The cultivated species of Nepenthes. The Gardeners' Chronicle and Agricultural Gazette 1872(16): 540–542.
  33. ^ 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
  34. ^ 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
  35. ^ Lowrie, A. 1983. Sabah Nepenthes Expeditions 1982 & 1983. Carnivorous Plant Newsletter 12(4): 88–95.
  36. ^ (in Indonesian) Akhriadi, P. 2007. Kajian taksonomi hibrid alami Nepenthes (Nepenthaceae) di Kerinci Archived 3 March 2016 at the Wayback Machine. Working paper, Andalas University, Padang. Abstract Archived 4 March 2016 at the Wayback Machine

Further reading

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