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Nerine

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This article is about the plant genus. For the anime character, see Nerine (Shuffle!).

Nerine /nɪˈraɪniː/[4] (nerines, Guernsey lily, Jersey lily, spider lily) is a genus of flowering plants belonging to the family Amaryllidaceae, subfamily Amaryllidoideae. They are bulbous perennials, some evergreen, associated with rocky and arid habitats. They bear spherical umbels of lily-like flowers in shades from white through pink to crimson. In the case of deciduous species, the flowers may appear on naked stems before the leaves develop. Native to South Africa, there are about 20–30 species in the genus. Though described as lilies, they are not significantly related to the true lilies (Liliaceae), but more closely resemble their relatives, Amaryllis and Lycoris. The genus was established by the Revd. William Herbert in 1820.

Nerine
Nerine sarniensis
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Monocots
Order: Asparagales
Family: Amaryllidaceae
Subfamily: Amaryllidoideae
Subtribe: Strumariinae
Genus: Nerine
Herb., nom. cons.[1][2]
Type species
Nerine sarniensis
(L.) Herb.
Species

See text

Synonyms[3]

Nerines have been widely cultivated and much hybridized worldwide, especially Nerine bowdenii, N. masoniorum, N. sarniensis and N. undulata (previously known as N. flexuosa). The hybrid cultivar 'Zeal Giant' has gained the Royal Horticultural Society's Award of Garden Merit. Most of the other 20 species are rarely cultivated and very little is known regarding their biology. Many species are threatened with extinction due to the loss or degradation of their habitat.

Description

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Figure 1. Morphological features
 
A. N. humilis: Style, 6 stamens, 6 wavy tepals with crisped margins
 
B. N. angustifolia: Umbellate inflorescence with flowers on pedicls
 
C. N. bowdenii: Flowers on leafless stem
 
D. N. filifolia: Filiform leaves

Species of Nerine are herbaceous perennial bulbous flowering plants. In the case of deciduous species, the inflorescence may appear on naked stems before the leaves develop (hysteranthy), otherwise they appear together with the flowers (synanthy) or afterwards.[5][6][7]

The bulbs may have a short neck, but this is absent in other species. The leaves are filiform (threadlike) (as in N. filifolia; Figure 1D) to linear and flat and strap-shaped (as in N. humilis; Figure 2C). Their flowers, which are few, are borne in spherical umbels on a solid leafless stem (scape or peduncle). The stem may be slender or robust, and rarely minutely puberulous (hairy), with two lanceolate (lance shaped) spathe-valves (spathal bracts) surrounding the inflorescence. The pedicels (flower stalks) may be glabrous (hairy) or smooth, a feature used in differentiating species.

Individual flowers are lily-like, generally with a perianth that is zygomorphic (with one plane of symmetry) but may be actinomorphic (radially symmetrical or "regular"). Each flower is flared, usually with a short extended or recurved perianth tube, consisting of six narrow white, pink or red tepals (perianth segments) joined at the base to form the tube. The free parts of the tepals are generally narrowly oblanceolate (wider near tip) and undulate (wavy) with crisped (curly) margins.[6][7]

The six stamens may be declinate (curvy) or erect, are unequal and are inserted into the base of the tepals, and are connate (fused) at their bases, frequently protruding from the flower. The stamen filaments are thin and filiform, but may be appendiculate (bearing appendages) at their base, a feature that is also important in differentiating species. Their anthers are versatile (swinging freely) and oblong and attach to the filament at the back (dorsifixed).[6][7] The pollen is bisulcate (two grooves).[8]

The inferior ovary is subglobose (slightly flattened sphere) and trilocular (three-lobed or three locules), with one to four ovules in each loculus. The style is filiform, straight or declinate and has an obscurely tricuspidate (three tipped) stigmatose apex.[6][7] The fruit is a subglobose dry loculicidal dehiscent capsule, that produces between one and a few seeds per loculus that are globose to ovoid, red-green and often viviparous (begin to develop before separating).[6][7][9]

Chromosome number: 11 (2n=22),[10][11][12][7] but rarely 2n=24 or triploids.[13][14]

Taxonomy

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History

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Herbert's 1820 illustration of N. rosea (N. sarniensis)

The first description was in 1635 by French botanist Jacques-Philippe Cornut, who examined Narcissus japonicus rutilo flor (N. sarniensis), a plant he found in the garden of the Paris nurseryman, Jean Morin in October 1634. In 1680 Scottish botanist Robert Morison gave an account of a shipment from Japan being washed ashore. In 1725 James Douglas FRS published an account in his A Description of the Guernsey Lilly,[15] as it was known then. Douglas gave it the Latin name Lilio-Narcissus Sarniensis Autumno florens.[16][a] Linnaeus called this Amaryllis sarniensis in 1753, after Douglas' usage, one of nine species he assigned to this genus.[14][17]

The earliest published name for the genus was Imhofia, given by Lorenz Heister in 1755.[18] The later name Nerine, published by William Herbert in 1820, was widely used, resulting in a decision to conserve the name Nerine and reject the name Imhofia (nom. rej.). Herbert was unaware of Heister's work initially in 1820, but noting that Heister had not defined it and it had not been adopted, transferred the name to Amaryllis marginata, retaining Nerine for N. sarniensis and renaming A. marginata Imhofia marginata (now Brunsvigia marginata).[19]

Herbert's main role was in untangling a number of distinct genera that Linnaeus had included under Amaryllis.[20][2] Although in Herbert's description of Nerine rosea there, he attempted to distinguish it from N. sarniensis, the former is now accepted as a synonym of the latter, the accepted name.[21] When Herbert chose the name of these nymphs for the first species of the genus, Nerine sarniensis, he alluded to the story of how this South African species arrived on the island of Guernsey in the English Channel. It is said that a ship carrying boxes of the bulbs of this species destined for the Netherlands was shipwrecked on Guernsey. The boxes of bulbs were washed up on the island and the bulbs became established and multiplied around the coast.[22] Herbert eventually recognised nine species. At that time Amaryllis (and hence Nerine) were placed in the family Amaryllideae, following the classification of de Candolle (1813).[23] Herbert's main interests were in the taxonomy of amaryllids, publishing a monograph on this in 1837,[24] considering Amaryllideae as one of seven suborders of Amaryllidaceae. He then further subdivided this suborder into groups, placing Nerine and Amaryllis together with twelve other genera into the Amaryllidiformes.[25] In his extensive treatment of Nerine he divided the nine species he recognised into two sections, Regulares and Distortae, of which only N. humilis and N. undulata are still in use. He had also begun a breeding program and described seven hybrids he had raised.[26] His enthusiasm for the genus is evident in that he chose to illustrate the front of the book with one of his hybrids, N. mitchamiae (see illustration).[27]

New species continued to be described so that by the time Traub published his monograph in 1967, he identified 30 species.[13] Other authors, including Norris (1974)[28] and Duncan (2002),[29][12] have identified 31 and 25 species respectively. At one stage 53 species were described.[30] Snijman and Linder (1996), who used a cladistic analysis of 33 characteristics and chromosome number, reduced this to 23, assigning many of these species to varietal status. They considered Nerine to be characterised by zygomorphic flowers with attenuated tepals and crisped margins.[31]

Phylogeny

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In the APG IV system (2016),[32] the genus Nerine is placed in the subfamily Amaryllidoideae of a broadly defined family Amaryllidaceae. Within the subfamily, Nerine is placed in the Southern African tribe Amaryllideae.[33] The phylogenetic relationships of the Amaryllideae have been investigated through molecular analysis of DNA combined with morphological data. This cladistic analysis has demonstrated that Nerine belongs to a monophyletic group forming subtribe Strumariinae. The members of this clade all originate from South Africa and often have prostrate leaves, fused stamens forming a tube towards the base of the flower, dehiscent fruit, and seeds with a well developed seed coat and chlorophyll. Within the Strumariinae, Nerine is most closely related to Brunsvigia Heist., Namaquanula D. & U. Müll.-Doblies and Hessea Herb.[14][34]

The genera of Strumariinae are related as in this cladogram, with number of species in each genus in (parentheses):[34]

Strumariinae

Nerine (~23)

Hessea (13)

Strumaria (24)

Crossyne (2)

Subdivision

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Attempts to generate an infrageneric classification (such as those of Traub's four sections and Norris' twelve groups) based on morphological characteristics alone relied on the presence of appendages to the bases of the stamen filaments, the presence of hairs on the ovary, scape and pedicels, together with the shape and arrangement of perianth segments.[14] Traub divided the genus into four subgeneric sections, Nerine, Laticomae, Bowdeniae and Appendiculatae. For instance the six taxa of Laticomae were grouped on the basis of filaments that were not distinctly appendiculate or otherwise modified at the base and scapes that were relatively short and stout.

Much of the modern understanding of the genus comes from the work of Graham Duncan and colleagues at SANBI, Kirstenbosch. In 2002 Duncan grouped the species of Nerine by growth cycle, with three distinct patterns.[29] [29] Nerine species can be either evergreen or deciduous, the deciduous species either growing during the winter or the summer. Zonnefeld and Duncan (2006)[14] examined the total amount of nuclear DNA by flow cytometry in 81 accessions from 23 species. When the species were arranged by DNA content, five groupings (A–E) were apparent, that correlated with growth cycle and leaf width, but only two of the other characteristics (filament appendages and hairy pedicels). Traub's sections were not confirmed, although a slightly better agreement was found with Norris' groups. Leaf width fell into two main groups, narrow (1–4 mm) or broad (6–37 mm). When taken together these characteristics confirm Duncan's original three groups based on growth cycle alone.

The first of these is the largest of these groups, corresponding to DNA groups A, B and C, with 13 species, and contains narrow-leafed evergreen nerines that retain their leaves throughout the summer and winter. They contain the lowest amount of DNA per nucleus. The second group corresponds to DNA group D with four broad-leafed deciduous winter growing species. They contain an intermediate amount of DNA. A third group (DNA group E) has six broad-leafed summer growing deciduous species that have no leaves in the winter. They contain the highest amount of DNA.[14] The two broad-leaved groups are also distinguished by the absence of filamentous appendages and glabrous pedicels, although two of the species have hairs on the pedicels, but these are minute or sparse.

The first group (the evergreens) can then be considered to have three subgroups corresponding to DNA groups A, B and C but also by other characteristics. N. marincowitzii is an outlier being summer growing but narrow-leafed. The other outlier is N. pusilla which is narrow-leafed despite being summer growing. N. duparquetiana has at times been considered to be a synonym of N. laticoma but was restored to species status here. N. huttoniae is another species whose status is disputed, but here is treated (as Traub did) as a subspecies of N. laticoma, a status subsequently confirmed.[35] Two species of doubtful status were not accessed, N. transvaalensis and N. hesseoides.[14]

Based on morphology, geography and DNA content they concluded that there were in fact 23 species, in contrast to the large number of subspecies considered by Traub.[36][14]

Species list

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As of 2016, the World Checklist of Selected Plant Families (WCLSPF) recognises 24 species[37] and The Plant List (TPL), 25[38] (for explanation of the discrepancy, see Notes). Species accepted by the WCLSPF and arranged sensu Zonnefeld & Duncan Table 2[14] are:[b]

Species assigned to other genera

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Hybrids

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Nerine hybrids, along with the parent species, where known, are the following:

Some Nerine species have been used to produce a hybrid with members of the genus Amaryllis, which are included in the hybrid genus (nothogenus) × Amarine. One of these hybrids is × Amarine tubergenii Sealy, which comes from a cross between Amaryllis belladonna and Nerine bowdenii.[37]

Etymology

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The genus name given to it by Herbert in 1820 derives from the Nereids (sea-nymphs) of Greek mythology that protected sailors and their ships. Herbert combined Morison's account of the plant being washed ashore from a shipwreck with Renaissance poetry, alluding to the rescue of Vasco da Gama’s ship by a Nereid in the epic poem of Camões, Os Lusiadas.[40] Although bearing the name "lily" in the vernacular, Nerine is only distantly related to the true lilies (Lilium) of the lily family, Liliaceae, sensu stricto. Instead they are one of many genera placed in the amaryllid lily family, Amaryllidaceae, such as the closely related Amaryllis, and Lycoris. These were once part of the much larger construction of Liliaceae sensu lato. The name "spider lily" is shared by a number of different genera within Amaryllidaceae. For instance, Lycoris aurea may be sold under its earlier synonym, Nerine aurea.[39]

Distribution and habitat

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Nerine are native to Southern Africa, their distribution range being from the Cape Peninsula in the south to Botswana, Eswatini, Lesotho, Namibia to the northwest and northeast of South Africa, occupying all nine provinces of South Africa. (see distribution maps in Zonneveld & Duncan, 2006).[14][22] They prefer rocky, arid and mesic habitats, and most species are found in the summer rainfall region.[31]

Ecology

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Nerine species form three distinct growth patterns, namely winter-growing, summer-growing and evergreen species.[22] While the flowers are generally pink, a red colour is an adaptation to a pollinator, the butterfly Aeropetes tulbaghia.[7]

Conservation

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N. masoniorum

Some Nerine species from Eastern Cape Province are naturally rare, but they are not considered to be in immediate danger of extinction. These include the winter-growing species N. pudica that inhabits inaccessible locations in the Du Toitskloof and Sonderend mountains, and the summer-growing N. marincowitzii that originates from the semi-arid Karoo region.

A number of evergreen nerine species from areas of South Africa that have summer rain are in danger due to the loss or degradation of their habitat and at least two or three of them are on the verge of extinction. Nerine masoniorum is probably the most critically threatened and it may even have become extinct as the area occupied by the only surviving colony has been used for the construction of housing.[41] Another species that is seriously threatened is N. gibsonii from Eastern Cape Province as the grasslands that it grows in have been seriously damaged by overgrazing and erosion resulting from the construction of paths and roads. In addition, this species rarely produces seeds as grazing cattle eat the flowers as soon as they appear.[42]

Various measures have been taken to relieve the threat of extinction from these species. One of these measures, thanks to their ease of cultivation, is the ex situ conservation of a number of populations of N. filamentosa, N. gibsonii, N. gracilis, N. huttoniae and N. masoniorum in the Kirstenbosch botanical garden.[43] Another measure, this time relating to in situ cultivation is the official protection of some species in nature reserves, such as has happened for N. platypetala in the south of Mpumalanga.[44]

In Guernsey, the national flower is Nerine sarniensis, and the island collection of nerines is seeking recognition by National Council for the Conservation of Plants and Gardens as a national collection.[45]

Cultivation

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William Herbert's hybrid, N. mitchamiae (left) from Frontispiece to his Amaryllidaceae 1837

Breeding and hybridisation of Nerine began as early as the beginning of the nineteenth century with the work of William Herbert. A number of the species of this genus are cultivated as ornamentals, such as N. sarniensis, N. undulata (N. flexuosa) and Nerine bowdenii.[12] N. sarniensis is, probably, the best known species of the genus and it has been cultivated in Europe since the beginning of the 17th century. N. bowdenii was introduced to England at the end of the 19th century and used as an ornamental since the first decade of the 20th century.[46] Along with Nerine bowdenii they have been extensively used in plant breeding programmes that have produced the majority of the commercially available hybrids.[11] The hybrid cultivar 'Zeal Giant' has gained the Royal Horticultural Society's Award of Garden Merit.[47]

The bulbs of Nerine species need a minimum of two years growth and development in order to produce their first flowers. The largest bulbs can give rise to two stems or more if they have been grown under suitable conditions. They are used as cut flowers as they can survive up to 14 days in a vase with water without showing any staining.[12]

Uses

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Nerine species and hybrids with their colourful long-lasting blooms are grown commercially for the cut-flower industry and sale of ornamental bulbs.[14][30]

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Figure 2. Other species
  •  
    A. N. angulata
  •  
    B. N. bowdwnii
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    C. N. humilis
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    D. N. mansellii
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    E. N. undulata

See also

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Notes

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  1. ^ Narcisso-Lirion Sarniense in the first edition, but adopting the continental usage Lilio-Narcissus Sarniensis Autumno florens in the second. He also used the term Lilium Sarniense vulgo as a common name[16]
  2. ^ Both include the hybrid Nerine x versicolor, which Zonnefeld & Duncan did not
  3. ^ Treated as N. laticoma subsp. laticoma by WCLSPF, but as species by Zonneveld & Duncan
  4. ^ Treated as species by TPL but as N. laticoma subsp. huttoniae by Zonneveld & Duncan and WCLSPF
  5. ^ Both accepted by WC:SPF and TPL
  6. ^ Probably subspecies or variety of N. frithii
  7. ^ Described in 1928 and not seen since, possible subspecies of N. frithii

References

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  1. ^ WCLSPF 2016, Nerine
  2. ^ a b Herbert 1820b.
  3. ^ WCLSPF 2016, Synonyms
  4. ^ SWGB 1995.
  5. ^ RHS 2008.
  6. ^ a b c d e Dyer 1975.
  7. ^ a b c d e f g Kubitzki 1998, Nerine p. 96
  8. ^ Dahlgren, Clifford & Yeo 1985, Amaryllideae p. 202
  9. ^ Byng 2014, Nerine p.86
  10. ^ Dimitri 1987.
  11. ^ a b Saunders 2013.
  12. ^ a b c d Duncan 2002b.
  13. ^ a b Traub 1967.
  14. ^ a b c d e f g h i j k Zonneveld & Duncan 2006.
  15. ^ Douglas 2012.
  16. ^ a b David 2012.
  17. ^ Linnaeus 1753, Amaryllis sarniensis pp. 293
  18. ^ Heister 1755, XLVIII Imhofia p. 29
  19. ^ Herbert 1821, Preliminary p. 3
  20. ^ Herbert 1820a.
  21. ^ WCLSPF 2016, N rosea
  22. ^ a b c PlantZAfrica 2016, Duncan: N. sarniensis
  23. ^ Candolle 1813, Esquisse. D'une Série linéaire et par conséquent artificielle, pour la disposition des familles naturelles du règne végetal p. 219
  24. ^ Herbert 1837.
  25. ^ Herbert 1837, p. 61
  26. ^ Herbert 1837, Nerine pp. 283–287
  27. ^ Herbert 1837, Frontispiece
  28. ^ Norris 1974.
  29. ^ a b c Duncan 2002a.
  30. ^ a b Brown 1999.
  31. ^ a b Snijman & Linder 1996.
  32. ^ APG IV 2016.
  33. ^ Stevens 2016, Amaryllideae
  34. ^ a b Meerow & Snijman 2001.
  35. ^ Duncan 2016.
  36. ^ Goldblatt 1972.
  37. ^ a b WCLSPF 2016.
  38. ^ TPL 2013, Nerine
  39. ^ a b WCLSPF 2016, N aurea
  40. ^ Coombes 2012.
  41. ^ Dold, Cloete & Weeks 2000.
  42. ^ Dold & McMaster 2004.
  43. ^ Duncan 2008.
  44. ^ Craib 1996.
  45. ^ "It's time nerines got more recognition". Guernsey Press. 4 April 2017.
  46. ^ David 2008.
  47. ^ RHS 2015, Nerine 'Zeal Giant'

Bibliography

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Historical sources

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Books

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Articles, symposia and theses

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Species

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Websites

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Organizations

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