Nepenthes neoguineensis

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Nepenthes neoguineensis
Lower pitchers of N. neoguineensis
from Western New Guinea

Least Concern  (IUCN 3.1)[1]
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Order: Caryophyllales
Family: Nepenthaceae
Genus: Nepenthes
Species:
N. neoguineensis
Binomial name
Nepenthes neoguineensis
Synonyms
  • Nepenthes leptoptera
    Zippel in sched. (1900)
Heterochresonyms

Nepenthes neoguineensis /nɪˈpɛnθiːz ˌniːoʊɡɪniˈɛnsɪs/ is a tropical pitcher plant native to the island of New Guinea, after which it is named.

Botanical history

Nepenthes neoguineensis was first collected in 1828 by Alexander Zipelius near Triton Bay, New Guinea.[note a] Two further collections were made by Gerard Versteeg [nl] on June 19[note b] and September 25, 1907.[note c] N. neoguineensis was again collected on May 10, 1910, by Knud Gjellerup.[note d][4]

The first name applied to this species was Nepenthes leptoptera by Hermann Zippel in 1900. However, this name is not valid as it only appeared on the label of a herbarium specimen (HLB.908.154-597) deposited at the National Herbarium of the Netherlands in Leiden.[5] The specimen was collected from New Guinea.[5]

Nepenthes neoguineensis was described by John Muirhead Macfarlane in 1911 based on the specimen Versteeg 1746, which consists of female plant material.[2]

In 1916,

B. H. Danser showed that it belonged to a closely related but distinct species, which he named N. papuana.[note e][4]

Description

Nepenthes neoguineensis is a climbing plant. The stem is up to 6 mm thick and cylindrical to obtusely angular in cross section, especially in the upper part of the internodes. Internodes are up to 4 cm long.[4]

Climbing stems with inflorescences

Leaves are

midrib. Pinnate veins ascend obliquely from the midrib and are irregularly reticulate in the outer part of the lamina. Tendrils are up to 4 mm thick and about as long as the lamina.[4]

Upper pitchers gradually arise from the ends of the tendrils, forming a 7 to 23 mm wide curve. They are

spur (≤3 mm long) is inserted at the base of the lid.[4]

Upper pitchers

The male

anthers.[4]

The female inflorescence is a panicle-like

ovary is sessile.[4]

Nepenthes neoguineensis has a very sparse indumentum. The stem is virtually glabrous, as is the lamina. Tendrils are densely hirsute when young, becoming only hairy near the pitcher or entirely glabrous when mature. Pitchers have a dense covering of caducous stellate hairs. The exception is the spur, which has persistent stellate hairs. Inflorescences have a very dense indumentum of short, white or brownish stellate hairs. The pedicels, tepals and the ovary are very densely stellate-tomentose.[4]

Lower pitchers range in colour from light green to dark purple throughout. Upper pitchers are generally yellowish-green, often with a darker peristome and bright red lid. Herbarium specimens are fallow-dun in colour.[4]

Ecology

Nepenthes neoguineensis growing in a clay-based substrate

Nepenthes neoguineensis is native to

Least Concern on the 2006 IUCN Red List of Threatened Species.[1]

Nepenthes neoguineensis grows on river edges, river gravel bars, ridge crests, and rarely in open grassland or disturbed forest. It has a wide altitudinal distribution, occurring from sea-level to an elevation of 900 m (3,000 ft), occasionally 1,400 m (4,600 ft).[1][7]

In the wild, N. neoguineensis occurs sympatrically with N. ampullaria and N. maxima.

Related species

An upper pitcher of N. papuana

Danser considered N. tomoriana from Sulawesi and N. distillatoria from Sri Lanka to be the closest relatives of N. neoguineensis. He also noted its similarity to N. papuana, stating: "N. papuana is so much alike N. neoguineensis in its vegetative parts, that only the complete knowledge of the generative parts has suggested me to establish a new species".[4]

The two taxa can be distinguished on the basis of several morphological features. N. papuana has a racemose inflorescence, while that of N. neoguineensis is a panicle or panicle-like raceme. Furthermore, the inflorescence of N. papuana usually bears only one-flowered pedicels, both in male and female plants. Those of N. neoguineensis can be up to four-flowered.[4]

The lamina of N. papuana has very distinct longitudinal veins and indistinct pinnate veins, whereas in N. neoguineensis the opposite is true. In addition, the leaves of N. papuana are very densely ciliate, much more so than in N. neoguineensis. The wings are less developed in the upper pitchers of N. papuana and the fringe elements are more closely spaced.[4]

Based on the structure of its inflorescence, it has been suggested that N. neoguineensis belongs to a group of relatively primitive Nepenthes species, which includes N. distillatoria and N. pervillei.[8]

Natural hybrids

A lower pitcher of N. ampullaria × N. neoguineensis (left) and a lower pitcher of N. maxima × N. neoguineensis (right)

Where their ranges overlap, N. neoguineensis is known to hybridise with N. ampullaria and N. maxima.[9] The hybrid plants are generally intermediate in appearance between their parent species.

Notes

a.^ Zippel 177 was collected in 1828 near Triton Bay. Zipelius explored this area between June and August and probably collected it during this time.[10] The habitat is recorded as "ad parietines humid, in convallibus montium". The specimen is deposited at Herbarium Lugduno-Batavum in Leiden. It does not include flowers or fruits.[4]
b.
Unir River) at an elevation of 30 m. It is deposited at the Bogor Botanical Gardens (formerly the Herbarium of the Buitenzorg Botanic Gardens) in Java. It does not include flowers or fruits.[4]
c.^ Versteeg 1746 was collected on September 25, 1907, on a "Nepenthes-hill". It is deposited at the Bogor Botanical Gardens and consists of female plant material.[4]
d.^ Gjellerup 122 was collected on May 10, 1910, in Hollandia at an elevation of 30 m. It is preserved in alcohol and deposited at the Bogor Botanical Gardens. It consists of male plant material.[4]
e.^ The Latin diagnosis for N. neoguineensis from Danser's monograph reads:[4]

Folia mediocria petiolata, lamina lanceolata, nervis longitudinalibus utrinque 3-4, vagina caulis 1/2 amplectente ; ascidia rosularum et inferiora ignota ; ascidia superiora mediocria, subcylindrica, sub medio et os versus paulum ampliata, alis 2 fimbriatis ; peristomio operculum versus acuminato, cylindrico v. applanato, 1-1 1/2 cm lato, costis 1/3-1/4 mm distantibus, dentibus fere 0 ; operculo suborbiculari, facie inferiore plano ; inflorescentia panicula v. racemus pedicellis inferioribus ad 35 mm longis 3-floris superioribus brevioribus, 2- v. 1-floris ; indumentum parcum villosum, in caulibus foliisque fere 0, in ascidiis iuventute densum, denique parcum, in inflorescentiis et floribus densum permanens.

References

  1. ^
    doi:10.2305/IUCN.UK.2018-1.RLTS.T39682A143962744.en
    . Retrieved 19 November 2021.
  2. ^ a b Macfarlane, J.M. 1911. Nepenthaceae. In: Nova Guinea 8(1): 339–341.
  3. ^
    doi:10.1111/j.1095-8339.1916.tb00009.x
  4. ^ a b c d e f g h i j k l m n o p q Danser, B.H. 1928. The Nepenthaceae of the Netherlands Indies. Bulletin du Jardin Botanique de Buitenzorg, Série III, 9(3–4): 249–438.
  5. ^ a b Schlauer, J. N.d. Nepenthes leptoptera. Carnivorous Plant Database.
  6. Field Guide to the Pitcher Plants of Australia and New Guinea
    . Redfern Natural History Productions, Poole.
  7. ^ Jebb, M.H.P. & M.R. Cheek 1997. A skeletal revision of Nepenthes (Nepenthaceae). Blumea 42(1): 1–106.
  8. ^ Nerz, J. Nepenthes neoguineensis. Joachim-Nerz.de.
  9. ^ McPherson, S.R. 2009. Pitcher Plants of the Old World. 2 volumes. Redfern Natural History Productions, Poole.
  10. ^ van Steenis-Kruseman, M.J., et al. 2006. Cyclopaedia of Malesian Collectors: Alexander Zip(p)elius. Nationaal Herbarium Nederland.

Further reading

External links

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