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Title: Asparagales  
Author: World Heritage Encyclopedia
Language: English
Subject: Amaryllidaceae, Allioideae, Lomandroideae, Monocotyledon, Orchidaceae
Collection: Angiosperm Orders, Asparagales, Late Cretaceous First Appearances
Publisher: World Heritage Encyclopedia


Asparagales is an order of plants in modern classification systems such as APG III (which is used throughout this article).[4] The order takes its name from the family Asparagaceae and is placed in the monocots. The order has only recently been recognized in classification systems. It was first put forward by Huber in 1977[5] and later taken up in the Dahlgren system of 1985.[6] Before this, many of its families were assigned to the old order Liliales: a very large order containing almost all monocots with colourful tepals and without starch in their endosperm. DNA sequence analysis indicated that Liliales should be divided into at least Liliales, Asparagales and Dioscoreales. The boundaries of the Asparagales and of its families have undergone a series of changes in recent years; future research may lead to further changes and ultimately greater stability.

The order is clearly circumscribed on the basis of DNA sequence analysis, but is difficult to define morphologically, since its members are structurally diverse. Thus although most species in the order are herbaceous, some no more than 15 cm high, there are a number of climbers (e.g., some species of Asparagus), as well as several genera forming trees (e.g. Agave, Cordyline, Yucca, Dracaena), some of which can exceed 10 m in height. Succulent genera occur in several families (e.g. Aloe).

One of the defining characteristics of the order is the presence of phytomelan (phytomelanin), a black pigment present in the seed coat, creating a dark crust. Phytomelan is found in most families of the Asparagales (although not in Orchidaceae, thought to be a sister to the rest of the group).

Almost all species have a tight cluster of leaves (a rosette), either at the base of the plant or at the end of a more-or-less woody stem; the leaves are less often produced along the stem. The flowers are in the main not particularly distinctive, being of a general 'lily type', with six tepals, either free or fused from the base.

The order is thought to have first diverged from other related monocots some 120–130 million years ago (early in the Cretaceous period),[7][8] although given the difficulty in classifying the families involved, estimates are likely to be uncertain.

From an economic point of view, the order Asparagales is second in importance within the monocots to the order Poales (which includes grasses and cereals). Species are used as food and flavourings (e.g. onion, garlic, leek, asparagus, vanilla), as cut flowers (e.g. freesia, gladiolus, iris, orchids), and as garden ornamentals (e.g. day lilies, lily of the valley, Agapanthus).


  • Description 1
  • Taxonomy 2
    • History 2.1
      • Pre-Darwinian 2.1.1
      • Post-Darwinian 2.1.2
      • Twentieth century 2.1.3
    • Phylogenetics 2.2
    • Phylogeny and APG system 2.3
      • Changes to family structure in APG III 2.3.1
    • Structure of Asparagales 2.4
      • Orchid clade 2.4.1
      • Boryaceae to Hypoxidaceae 2.4.2
      • Ixioliriaceae to Xeronemataceae 2.4.3
      • Xanthorrhoeaceae sensu lato + 'core Asparagales' 2.4.4
    • Evolution 2.5
    • Subdivision 2.6
      • Comparison of family structures 2.6.1
  • Uses 3
  • See also 4
  • Notes 5
  • References 6
  • Bibliography 7
    • APG 7.1
    • Historical sources 7.2
    • Reference materials 7.3


Seeds of Hippeastrum with dark phytomelan-containing coat
Tree-like habit created by secondary thickening in Nolina recurvata

Most species of Asparagales are herbaceous perennials, although some are climbers (e.g. species of Asparagus, family Asparagaceae) and some are tree-like. The order also contains many geophytes (bulbs, corms and various kinds of tuber). Almost all species have a tight cluster of leaves (a rosette) at the base of the plant or, in the tree-forming species, at the end of a woody stem. Only in a few cases are leaves produced along the length of the stem. The flowers are often at the tip of the stem and are mainly of a rather generalized 'lily type', with six tepals and up to six stamens.

The orders which have been separated from the old Liliales are difficult to characterize. No single morphological character appears to be diagnostic of the order Asparagales.

  • The flowers of Asparagales are of a general type among the lilioid monocots. Compared to Liliales, they usually have plain tepals without markings in the form of dots. If nectaries are present, they are in the septa of the ovaries rather than at the base of the tepals or stamens.
  • Those species which have relatively large dry seeds have a dark, crust-like (crustose) outer layer containing the pigment phytomelan. However, some species with hairy seeds (e.g. Eriospermum, family Asparagaceae s.l.), berries (e.g. Maianthemum, family Asparagaceae s.l.), or highly reduced seeds (e.g. orchids) lack this dark pigment in their seed coats. Phytomelan is not unique to Asparagales (i.e. it is not a synapomorphy) but it is common within the order and rare outside it.[9] The inner portion of the seed coat is usually completely collapsed. In contrast, the morphologically similar seeds of Liliales have no phytomelan, and usually retain a cellular structure in the inner portion of the seed coat.
  • Most monocots are unable to thicken their stems once they have formed, since they lack the cylindrical meristem present in other angiosperm groups. Asparagales have a method of secondary thickening which is otherwise only found inDioscorea (in the order Disoscoreales). In a process called 'anomalous secondary growth', they are able to create new vascular bundles around which thickening growth occurs.[10] Agave, Yucca, Aloe, Dracaena, Nolina and Cordyline can become massive trees, albeit not of the height of the tallest dicots, and with less branching.[9] Other genera in the order, such as Lomandra and Aphyllanthes, have the same type of secondary growth but confined to their underground stems.
  • Microsporogenesis (part of pollen formation) distinguishes some members of Asparagales from Liliales. Microsporogenesis involves a cell dividing twice (meiotically) to form four daughter cells. There are two kinds of microsporogenesis: successive and simultaneous (although intermediates exist). In successive microsporogenesis, walls are laid down separating the daughter cells after each division. In simultaneous microsporogenesis, there is no wall formation until all four cell nuclei are present. Liliales all have successive microsporogenesis, which is thought to be the primitive condition in monocots. It seems that when the Asparagales first diverged they developed simultaneous microsporogenesis, which the 'lower' Asparagale families retain. However, the 'core' Asparagales (see #Phylogeny section) have reverted to successive microsporogenesis.[11]
  • The Asparagales appear to be unified by a mutation affecting their telomeres (a region of repetitive DNA at the end of a chromosome). The typical 'Arabidopsis-type' sequence of bases has been fully or partially replaced by other sequences, with the 'human-type' predominating.[12]
  • Other apomorphic characters of the order according to Stevens are: the presence of chelidonic acid, anthers longer than wide, tapetal cells bi- to tetra-nuclear, tegmen not persistent, endosperm helobial, and loss of mitochondrial gene sdh3.[1]


Asparagales represent the largest order within the monocotyledons, representing between 25,000–42,000 species, thus accounting for about 50% of all monocots and 10–15% of the flowering plants (angiosperms).[13] The attribution of botanical authority for the name Asparagales belongs to Johann Heinrich Friedrich Link (1767 – 1851) who coined the word 'Asparaginae' in 1829 for a higher order taxon that included Asparagus[14] although Adanson and Jussieau had also done so earlier (see History). Earlier circumscriptions of Asparagales attributed the name to Bromhead (1838), who had been the first to use the term 'Asparagales'.[3]



The [27]

The literature on the organisation of genera into families and higher ranks became available in the English language with [29]

Amaryllidaceae: Narcisseae - Pancratium maritimum Linn. John Lindley, Vegetable Kingdom 1846

The [31] divided into two tribes, the Petaloidea and Glumaceae. He divided the former, often referred to as petaloid monocots, into 32 orders, including the Liliaceae (defined narrowly), but also most of the families considered to make up the Asparagales today, including the Amaryllideae.

By 1846, in his final scheme[32] Lindley had greatly expanded and refined the treatment of the monocots, introducing both an intermediate ranking (Alliances) and tribes within orders (i.e. families). Lindley placed the Liliaceae within the [34] into four tribes (with 68 genera), yet both contained many genera that would eventually segregate to each other's contemporary orders (Liliales and Asparagales respectively). The Liliaceae would be reduced to a small 'core' represented by the Tulipae tribe, while large groups such Scilleae and Asparagae would become part of Asparagales either as part of the Amaryllidaceae or as separate families. While of the Amaryllidaceae, the Agaveae would be part of Asparagaceae but the Alstroemeriae would become a family within the Liliales.

The number of known genera (and species) continued to grow and by the time of the next major British classification, that of [38] as a distinct tribe that would eventually find its way to the Asparagales as the Allioideae subfamily of the Amaryllidaceae.


The appearance of Charles Darwin's Origin of Species in 1859 changed the way that taxonomists considered plant classification, incorporating evolutionary information into their schemata. The Darwinian approach led to the concept of phylogeny (tree-like structure) in assembling classification systems, starting with Eichler.[39] Eichler, having established a hierarchical system in which the flowering plants (angiosperms) were divided into monocotyledons and dicotyledons, further divided into former into seven ordewrs. Within the Liliiflorae were seven families, including Liliaceae and Amaryllidaceae. Liliaceae included Allium and Ornithogalum (modern Allioideae) and Asparagus.[40]

[45] In the Amaryllidacea, there was little change from Bentham and Hooker. A similar approach was adopted by Wettstein.[46]

Twentieth century

Longitudinal section of Narcissus poeticus, R Wettstein Handbuch der Systematischen Botanik 1901–1924
In the twentieth century the [49][5]

The widely used Cronquist system (1968–1988)[50][51][52] used the very broadly defined order Liliales.

These various proposals to separate small groups of genera into more homogeneous families, made little impact till that of herbaria. That committee finally recommended that 24 new families be created in the place of the original broad Liliaceae, largely by elevating subfamilies to the rank of separate families.[56]


The order Asparagales as currently circumscribed has only recently been recognized in classification systems, through the advent of phylogenetics. The 1990s saw considerable progress in plant phylogeny and phylogenetic theory, enabling a phylogenetic tree to be constructed for all of the flowering plants. The establishment of major new clades necessitated a departure from the older but widely used classifications such as Cronquist and Thorne based largely on morphology rather than genetic data. This complicated discussion about plant evolution and necessitated a major restructuring.[57] rbcL gene sequencing and cladistic analysis of monocots had redefined the Liliales in 1995.[58][59] from four morphological orders sensu Dahlgren. The largest clade representing the Liliaceae, all previously included in Liliales, but including both the Calochortaceae and Liliaceae sensu Tamura. This redefined family, that became referred to as core Liliales, but corresponded to the emerging circumscription of the Angiosperm Phylogeny Group (1998).[60]

Phylogeny and APG system

The 2009 revision of the Angiosperm Phylogeny Group system, APG III, places the order in the clade monocots.[4]

From the Dahlgren system of 1985 onwards, studies based mainly on morphology had identified the Asparagales as a distinct group, but had also included groups now located in Liliales, Pandanales and Zingiberales.[6] Research in the 21st century has supported the monophyly of Asparagales, based on morphology, 18S rDNA, and other DNA sequences,[61][62][63][64][65] although some phylogenetic reconstructions based on molecular data have suggested that Asparagales may be paraphyletic, with Orchidaceae separated from the rest.[66] Within the monocots, Asparagales is the sister of the commelinid clade.[57]

A possible phylogenetic tree for the Asparagales, including those families recently reduced to subfamilies, is shown below.[1]




Hypoxidaceae s.l.










Xanthorrhoeaceae s.l.

Hemerocallidoideae (= Hemerocallidaceae)

Xanthorrhoeoideae (= Xanthorrhoeaceae s.s.)

Asphodeloideae (= Asphodelaceae)

'core' Asparagales
Amaryllidaceae s.l.

Agapanthoideae (= Agapanthaceae)

Allioideae (= Alliaceae s.s.)

Amaryllidoideae (= Amaryllidaceae s.s.)

Asparagaceae s.l.

Aphyllanthoideae (= Aphyllanthaceae)

Brodiaeoideae (= Themidaceae)

Scilloideae (= Hyacinthaceae)

Agavoideae (= Agavaceae)

Lomandroideae (= Laxmanniaceae)

Asparagoideae (= Asparagaceae s.s.)

Nolinoideae (= Ruscaceae)

The tree shown above can be divided into a basal paraphyletic group, the 'lower Asparagales', from Orchidaceae to Xanthorrhoeaceae sensu lato,[67] and a well-supported monophyletic group of 'core Asparagales', comprising Amaryllidaceae sensu lato and Asparagaceae sensu lato.[1]

Two differences between these two groups (although with exceptions) are: the mode of microsporogenesis and the position of the ovary. The 'lower Asparagales' typically have simultaneous microsporogenesis (i.e. cell walls develop only after both meiotic divisions), which appears to be an apomorphy within the monocots, whereas the 'core Asparagales' have reverted to successive microsporogenesis (i.e. cell walls develop after each division).[61] The 'lower Asparagales' typically have an inferior ovary, whereas the 'core Asparagales' have reverted to a superior ovary. A 2002 morphological study by Rudall treated possessing an inferior ovary as a synapomorphy of the Asparagales, stating that reversions to a superior ovary in the 'core Asparagales' could be associated with the presence of nectaries below the ovaries.[68] However, Stevens notes that superior ovaries are distributed among the 'lower Asparagales' in such a way that it is not clear where to place the evolution of different ovary morphologies. The position of the ovary seems a much more flexible character (here and in other angiosperms) than previously thought.[1]

Changes to family structure in APG III

The APG III system when it was published in 2009, greatly expanded the families Xanthorrhoeaceae, Amaryllidaceae, and Asparagaceae.[69] Thirteen of the families of the earlier APG II system were thereby reduced to subfamilies within these three families. The APG II families (left) and their equivalent APG III subfamilies (right) are as follows:


Structure of Asparagales

Orchid clade

Orchidaceae is the largest family of all angiosperms and hence by far the largest in the order. The Dahlgren system recognized three families of orchids, but DNA sequence analysis later showed that these families are polyphyletic and so should be combined. Several studies suggest (with high bootstrap support) that Orchidaceae is the sister of the rest of the Asparagales.[63][64][65][70] Other studies have placed the orchids differently in the phylogenetic tree, generally among the Boryaceae-Hypoxidaceae clade.[7][61][58][71][72] The position of Orchidaceae shown above seems the best current hypothesis,[1] but cannot be taken as confirmed.

Orchids have simultaneous microsporogenesis and inferior ovaries, two characters that are typical of the 'lower Asparagales'. However, their nectaries are rarely in the septa of the ovaries, and most orchids have dust-like seeds, atypical of the rest of the order. (Some members of Vanilloideae and Cypripedioideae have crustose seeds, probably associated with dispersal by birds and mammals that are attracted by fermenting fleshy fruit releasing fragrant compounds, e.g. vanilla.)

In terms of the number of species, Orchidaceae diversification is remarkable. However, although the other Asparagales may be less rich in species, they are more variable morphologically, including tree-like forms.

Boryaceae to Hypoxidaceae

The four families excluding Boryaceae form a well-supported clade in studies based on DNA sequence analysis. All four contain relatively few species, and it has been suggested that they be combined into one family under the name Hypoxidaceae sensu lato.[73] The relationship between Boryaceae (which includes only two genera, Borya and Alania), and other Asparagales has remained unclear for a long time. The Boryaceae are mycorrhizal, but not in the same way as orchids. Morphological studies have suggested a close relationship between Boryaceae and Blandfordiaceae.[61] There is relatively low support for the position of Boryaceae in the tree shown above.[63]

Ixioliriaceae to Xeronemataceae

The relationship shown between Ixioliriaceae and Tecophilaeaceae is still unclear. Some studies have supported a clade of these two families,[63] others have not.[7] The position of Doryanthaceae has also varied, with support for the position shown above,[64] but also support for other positions.[63]

The clade from Iridaceae upwards appears to have stronger support. All have some genetic characteristics in common, having lost Arabidopsis-type telomeres.[74] Iridaceae is distinctive among the Asparagales in the unique structure of the inflorescence (a ripidium), the combination of an inferior ovary and three stamens, and the common occurrence of unifacial leaves whereas bifacial leaves are the norm in other Asparagales.

Members of the clade from Iridaceae upwards have infra-locular septal nectaries, which Rudall interpreted as a driver towards secondarily superior ovaries.[68]

Xanthorrhoeaceae sensu lato + 'core Asparagales'

The next node in the tree (Xanthorrhoeaceae sensu lato + the 'core Asparagales') has strong support.[75] 'Anomalous' secondary thickening occurs among this clade, e.g. in Xanthorrhoea (family Xanthorrhoeaceae sensu lato) and Dracaena (family Asparagaceae sensu lato), with species reaching tree-like proportions.

The 'core Asparagales', comprising Amaryllidaceae sensu lato and Asparagaceae sensu lato, are a strongly supported clade,[64] as are clades for each of the families. Relationships within these broadly defined families appear less clear, particularly within the Asparagaceae sensu lato. Stevens notes that most of its subfamilies are difficult to recognize, and that significantly different divisions have been used in the past, so that the use of a broadly defined family to refer to the entire clade is justified.[1] Thus the relationships among subfamilies shown above, based on APWeb as of December 2010, is somewhat uncertain.


Several studies have attempted to date the evolution of the Asparagales, based on phylogenetic evidence. Earlier studies[76][77] generally give younger dates than more recent studies,[7][8] which have been preferred in the table below.

Approx. date in
Millions of Years Ago
133-120 Origin of Asparagales, i.e. first divergence from other monocots[7][8]
93 Split between Xanthorrhoeaceae sensu lato and the 'core group' Asparagales[7]
91–89 Origin of Alliodeae and Asparagoideae[7]
47 Divergence of Agavoideae and Nolinoideae[76]

A 2009 study suggests that the Asparagales have the highest diversification rate in the monocots, about the same as the order Poales, although in both orders the rate is little over half that of the eudicot order Lamiales, the clade with the highest rate.[8]


The taxonomic diversity of the monocotyledons is described in detail by Kubitzki.[78][79] Up-to-date information on the Asparagales can be found on the Angiosperm Phylogeny Website.[1]

Comparison of family structures

The APG III system's family circumscriptions are being used as the basis of the Kew-hosted World Checklist of Selected Plant Families.[80] With this circumscription, the order consists of 14 families (Dahlgren had 31)[53] with approximately 1120 genera and 26000 species.[1]

Order Asparagales Link

  • Family Amaryllidaceae J.St.-Hil. (including Agapanthaceae F.Voigt, Alliaceae Borkh.)[notes 1]
  • Family Asparagaceae Juss. (including Agavaceae Dumort. [which includes Anemarrhenaceae, Anthericaceae, Behniaceae and Herreriaceae], Aphyllanthaceae Burnett, Hesperocallidaceae Traub, Hyacinthaceae Batsch ex Borkh., Laxmanniaceae Bubani, Ruscaceae M.Roem. [which includes Convallariaceae] and Themidaceae Salisb.)
  • Family Asteliaceae Dumort.
  • Family Blandfordiaceae R. Dahlgren & Clifford
  • Family Boryaceae M.W. Chase, Rudall & Conran
  • Family Doryanthaceae R. Dahlgren & Clifford
  • Family Hypoxidaceae R.Br.
  • Family Iridaceae Juss.
  • Family Ixioliriaceae Nakai
  • Family Lanariaceae R. Dahlgren & A.E.van Wyk
  • Family Orchidaceae Juss.
  • Family Tecophilaeaceae Leyb.
  • Family Xanthorrhoeaceae Dumort. (including Asphodelaceae Juss. and Hemerocallidaceae R.Br.)
  • Family Xeronemataceae M.W. Chase, Rudall & M.F.Fay

The earlier 2003 version, APG II, allowed 'bracketed' families, i.e. families which could either be segregated from more comprehensive families or could be included in them. These are the families given under "including" in the list above. APG III does not allow bracketed families, requiring the use of the more comprehensive family; otherwise the circumscription of the Asparagales is unchanged. A separate paper accompanying the publication of the 2009 APG III system provided subfamilies to accommodate the families which were discontinued.[81] The first APG system of 1998 contained some extra families, included in square brackets in the list above.

Two older systems which use the order Asparagales are the Dahlgren system[6] and the Kubitzki system.[78] The families included in the circumscriptions of the order in these two systems are shown in the first and second columns of the table below. The equivalent family in the modern APG III system (see below) is shown in the third column. Note that although these systems may use the same name for a family, the genera which it includes may be different, so the equivalence between systems is only approximate in some cases.

Families included in Asparagales in three systems which use this order
Dahlgren system Kubitzki system APG III system
Agapanthaceae Amaryllidaceae: Agapanthoideae
Agavaceae Asparagaceae: Agavoideae
Alliaceae Amaryllidaceae: Allioideae
Amaryllidaceae Amaryllidaceae: Amaryllidoideae
Anemarrhenaceae Asparagaceae: Agavoideae
Anthericaceae Asparagaceae: Agavoideae
Aphyllanthaceae Asparagaceae: Aphyllanthoideae
Asparagaceae Asparagaceae: Asparagoideae
Asphodelaceae Xanthorrhoeaceae: Asphodeloideae
Asteliaceae Asteliaceae
Behniaceae Asparagaceae: Agavoideae
Blandfordiaceae Blandfordiaceae
Boryaceae Boryaceae
Calectasiaceae Not in Asparagales (family Dasypogonaceae, unplaced as to order, clade commelinids)
Convallariaceae Asparagaceae: Nolinoideae
Cyanastraceae Tecophilaeaceae
Dasypogonaceae Not in Asparagales (family Dasypogonaceae, unplaced as to order, clade commelinids)
Doryanthaceae Doryanthaceae
Dracaenaceae Asparagaceae: Nolinoideae
Eriospermaceae Asparagaceae: Nolinoideae
Hemerocallidaceae Xanthorrhoeaceae: Hemerocallidoideae
Herreriaceae Asparagaceae: Agavoideae
Hostaceae Asparagaceae: Agavoideae
Hyacinthaceae Asparagaceae: Scilloideae
Hypoxidaceae Hypoxidaceae
Iridaceae Iridaceae
Ixioliriaceae Ixioliriaceae
Johnsoniaceae Xanthorrhoeaceae: Hemerocallidoideae
Lanariaceae Lanariaceae
Luzuriagaceae Not in Asparagales (family Alstroemeriaceae, order Liliales)
Lomandraceae Asparagaceae: Lomandroideae
Nolinaceae Asparagaceae: Nolinoideae
Orchidaceae Orchidaceae
Philesiaceae Not in Asparagales (family Philesiaceae, order Liliales)
Phormiaceae Xanthorrhoeaceae: Hemerocallidoideae
Ruscaceae Asparagaceae: Nolinoideae
Tecophilaeaceae Tecophilaeaceae
Themidaceae Asparagaceae: Brodiaeoideae
Xanthorrhoeaceae Xanthorrhoeaceae: Xanthorrhoeoideae


The Asparagales include many important crop plants and ornamental plants. Crops include Allium, Asparagus and Vanilla, while ornamentals include irises, hyacinths and orchids.[13]

See also


  1. ^ The name 'Alliaceae' has also been used for the expanded family comprising the Alliaceae sensu stricto, Amaryllidaceae and Agapanthaceae (e.g. in the APG II system). 'Amaryllidaceae' is used as a conserved name in APG III.


  1. ^ a b c d e f g h i Stevens 2015: Asparagales
  2. ^ Tropicos 2015
  3. ^ a b Bromhead 1838, p. 132
  4. ^ a b Angiosperm Phylogeny Group III 2009
  5. ^ a b Huber 1977
  6. ^ a b c Dahlgren, Clifford & Yeo 1985
  7. ^ a b c d e f g Janssen & Bremer 2004
  8. ^ a b c d Magallón & Castillo 2009
  9. ^ a b Chase 2004
  10. ^ Rudall 1995
  11. ^ Furness & Rudall 1999
  12. ^ Sýkorová et al. 2003
  13. ^ a b Chen et al. 2013
  14. ^ Link 1829, Asparaginae I: 272
  15. ^ Linnaeus 1753, Aparagus vol. i p. 325
  16. ^ Linnaeus 1753, Hexandria monogynia vol. i pp.  285–352
  17. ^ Lobstein 2013
  18. ^ Adanson 1763, Liliaceae: V Asparagi pp. 51–52
  19. ^ Jussieu 1789
  20. ^ Jussieu 1789, Stamina Perigynia p. 35
  21. ^ Jussieu 1789, Asparagi pp. 40–43
  22. ^ ICN 2011, Names of families and subfamilies, tribes and subtribes p. 18.2
  23. ^ de Candolle 1813, Des familles et des tribus pp. 192–195
  24. ^ Privat-Deschanel & Focillon 1870, Asparagi p. 291
  25. ^ Jaume Saint-Hilaire 1805, Amaryllidées vol. 1. pp. 134–142
  26. ^ Brown 1810, Prodromus. Amaryllideae p. 296
  27. ^ de Candolle 1813, Théorie élémentaire de la botanique p. 219
  28. ^ Gray 1821
  29. ^ Gray 1821,
  30. ^ Lindley 1830
  31. ^ Lindley 1830, Endogenae, or Monocotyledonous Plants p. 251
  32. ^ Lindley 1846)
  33. ^ Lindley 1846, Liliaceae - Lilyworts p. 200
  34. ^ Lindley 1846, Amaryllidaceae - Amaryllids p. 155
  35. ^ Bentham & Hooker 1883
  36. ^ Bentham & Hooker 1883, Liliaceae p. 748
  37. ^ Bentham & Hooker 1883, Amaryllideae p. 711
  38. ^ Bentham & Hooker 1883, Allieae p. 798
  39. ^ Stuessy 2009, Phyletic (evolutionary) classification p. 47
  40. ^ Eichler 1886, Liliiflorae p. 34
  41. ^ Engler & Prantl 1888
  42. ^ Engler 1903
  43. ^ Engler & Prantl 1888, Liliaceae II(5) pp. 10–91
  44. ^ Engler & Prantl 1888, Amaryllidaceae II(5) pp. 97–124
  45. ^ Engler 1903, Subfamily Allioideae p. 96
  46. ^ Wettstein 1924, Liliiflorae p. 862
  47. ^ Wettstein 1924, p.862
  48. ^ Lotsy 1911, Liliifloren: Asparaginaceae p. 743
  49. ^ Huber 1969, Die asparagoiden Liliifloren p. 304
  50. ^ Cronquist 1968
  51. ^ Cronquist 1981
  52. ^ Cronquist 1988
  53. ^ a b Dahlgren, Clifford & Yeo 1985, Order Asparagales
  54. ^ Walters & Keil 1996
  55. ^ Kelch 2002
  56. ^ Mathew 1989
  57. ^ a b Angiosperm Phylogeny Group II 2003
  58. ^ a b Chase et al. 1995
  59. ^ Rudall et al. (1995).
  60. ^ Patterson & Givnish 2002
  61. ^ a b c d Rudall 2002a
  62. ^ Davis et al. 2004
  63. ^ a b c d e Chase et al. 2006
  64. ^ a b c d Graham et al. 2006
  65. ^ a b Pires et al. 2006
  66. ^ Hilu et al. 2003
  67. ^ Rudall et al. 1997
  68. ^ a b Rudall 2002b
  69. ^ Chase et al 2009
  70. ^ Givnish et al. 2006
  71. ^ McPherson & Graham 2001
  72. ^ Li & Zhou 2007
  73. ^ Soltis et al. 2005
  74. ^ Fay 2000
  75. ^ Chase et al. 2000
  76. ^ a b Eguiarte 1995
  77. ^ Wikström, Savolainen & Chase 2001
  78. ^ a b Kubitzki 1998
  79. ^ Kubitzki 2006
  80. ^ WCSP 2010
  81. ^ Chase, Reveal & Fay 2009


  • In Rudall et al. (1995).
  • in Wilson & Morrison (2000)
  • : Families included in the checklist


Historical sources

Reference materials

  • Media related to at Wikimedia Commons
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