History Pre-Darwinian Linnaeus described the
type genus Amaryllis, from which the family derives its name, in his
Species Plantarum in 1753, with nine species, in the
Hexandria monogynia (i.e. six
stamens and one
pistil) containing 51 genera in total in his
sexual classification scheme. The name
Amaryllis had been applied to a number of plants over the course of history.
Hexandria monogynia has come to be treated as either liliaceous or amaryllidaceaeous (see
Taxonomy of Liliaceae) over time. From 1763, when
Michel Adanson conceived of these genera as '
Liliaceae' it was included in this family, placing
Amaryllis in Section VII, Narcissi of
his scheme, in which the Liliaceae had eight sections. With
de Jussieu came the formal establishment of organising genera into families (
ordo) in 1789. De Jussieu established the
hierarchical system of
taxonomy (
phylogeny), placing
Amaryllis and 15 related genera within a
division of
monocotyledons, a
class (III) of
Stamina Perigynia and 'order' Narcisse, divided into three subfamilies. This system also formally described the Liliaceae, which were a separate order within the
Stamina perigynia (Lilia). The use of the term
Ordo (order) at that time was closer to what we now understand as family, rather than order. In creating
his scheme, De Jussieu used a modified form of Linnaeus' sexual classification, but with the respective topography of stamens to carpels rather than just their numbers. The family Amaryllidaceae was formally named as 'Amaryllidées' (Amaryllideae) in 1805, by
Jean Henri Jaume Saint-Hilaire. In 1810
Brown proposed that a subgroup of Liliaceae be distinguished on the basis of the position of their ovaries (inferior) and be referred to as Amaryllideae and in 1813
de Candolle described Liliacées Juss. and Amaryllidées Brown as two quite separate families. The literature on the organisation of genera into families and higher ranks became available in the English language with
Samuel Frederick Gray's
A natural arrangement of British plants (1821). Gray used a combination of Linnaeus' sexual classification and Jussieu's natural classification to group together a number of families having in common six equal stamens, a single style and a perianth that was simple and petaloid, but did not use formal names for these higher ranks. Within the grouping, he separated families by the characteristics of their fruit and seed. He treated groups of genera with these characteristics as separate families, such as Amaryllideae, Liliaceae, Asphodeleae, and Asparageae.
John Lindley (1830, 1846) was the other important British taxonomist of the early 19th century. In his
first taxonomic work,
An Introduction to the Natural System of Botany (1830), he partly followed De Jussieu by describing a subclass he called 'Endogenae, or Monocotyledonous Plants' (preserving de Candolle's
Endogenæ phanerogamæ) divided into two tribes, the
Petaloidea and
Glumaceae. He divided the former, often referred to as petaloid monocots, into 32 orders, including the Amaryllideae. He defined the latter as "Hexapetaloideous bulbous hexandrous monocotyledons, with an inferior ovarium, a six-parted perianthium with equitant sepals, and flat, spongy seeds" and included
Amaryllis,
Phycella,
Nerine,
Vallota, and
Calostemma. By 1846, in his final scheme Lindley had greatly expanded and refined the treatment of the monocots, introducing both an intermediate ranking (Alliances) and tribes within families. Lindley placed the Liliaceae within the
Liliales, but saw it as a
paraphyletic ("catch-all") family, being all Liliales not included in the other orders, but hoped that the future would reveal some characteristic that would group them better. This kept the Liliaceae separate from the Amaryllidaceae (Narcissales Alliance). Of these, Liliaceae was divided into eleven tribes (with 133 genera) and Amaryllidaceae 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 tribe
Tulipeae (18 genera), 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 four tribes of the Amaryllidaceae, the Amaryllideae and Narcisseae would remain as core amaryllids while the
Agaveae would be part of Asparagaceae, but the
Alstroemeriae would become a family within the
Liliales. Since then, seven of Linnaeus'
Hexandria monogynia genera have consistently been placed in a common taxonomic unit of amaryllids, based on the
inferior position of the ovaries (whether this be as an order, suborder, family, subfamily, tribe or section). Thus, much of what we now consider Amaryllidaceae remained in Liliaceae because the ovary was superior, till 1926 when
John Hutchinson transferred them to Amaryllidaceae. This usage of the family entered the English language literature through the work of
Samuel Frederick Gray (1821),
William Herbert (1837) and
John Lindley (1830, 1846). Meanwhile, Lindley had described two
Chilean genera which for which he created a new family,
Gilliesieae. The number of known genera within these families continued to grow, and by the time of the
Bentham and Hooker classification (1883), the Amaryllidaceae (Amaryllideae) were divided into four tribes, of which only one (Amarylleae) is still included. The Liliaceae were becoming one of the largest families, and
Bentham and
Hooker divided it into 20 tribes, of which one was the Allieae, which as
Allioideae would eventually become part of Amaryllidaceae as two of its three subfamilies. The Allieae included both
Agapantheae, the third of the current subfamilies, and Lindley's
Gilliesieae as two of its four subtribes. Bentham and Hooker's scheme was the last major classification using the natural approach.
Post-Darwinian Although
Charles Darwin's
Origin of Species (1859) preceded Bentham and Hooker's publication, the latter project was commenced much earlier and
Bentham was initially sceptical of
Darwinism. The new
phyletic approach changed the way that taxonomists considered plant classification, incorporating
evolutionary information into their schemata. The major works in the late 19th and early 20th centuries employing this approach were German, those of
Eichler (1875–1886),
Engler,
Prantl (1886–1924), and
Wettstein (1901–1935). The Amaryllidaceae were treated similarly in the German-language literature to the manner they had been in English.
August Eichler (1886) was the first phyletic taxonomist and positioned the Amaryllidaceae and Liliaceae within the
Liliiflorae, one of the seven orders of monocotyledons. Liliaceae included both
Allium and
Ornithogalum (modern
Allioideae).
Adolf Engler developed Eichler's ideas much further, into much more elaborate schemes that evolved over time, from his 1888 scheme, contributed by
Pax to his 1903 version. In the latter, the Liliineae were a suborder of Liliiflorae, including both families Liliaceae and Amaryllidaceae. Within the Liliaceae, the core liliids were segregated in subfamily
Lilioideae from the alliaceous subfamily,
Allioideae.
Allieae,
Agapantheae, and
Gilliesieae were the three tribes within this subfamily. A somewhat similar approach to Liliiflorae was adopted by
Wettstein (without suborders or tribes), and with Alliodeae (
Allium) and
Lilioideae (
Ornithogalum) as subfamilies of Liliaceae. Wettstein's Amaryllidaceae contained three subfamilies, including Amaryllidoideae and Agavoideae.
, R Wettstein Handbuch der Systematischen Botanik'' 1901–1924 The early 20th century was marked by increasing doubts about the placement of the alliaceous genera within Liliaceae.
Lotsy was the first taxonomist to propose separating them, and in his system he describes Agapanthaceae, Alliaceae, and Gilliesiaceae as new and separate families from Liliaceae. This approach was adopted by a number of other authorities, such as Dahlgren (1985) and Rahn (1998). Another approach was that of
John Hutchinson (1926), who performed the first major
recircumscription of the family in over a century. He doubted Brown's dictum that the position of the ovary was the distinguishing feature that separated Amaryllidaceae and Liliaceae. He treated Amaryllidaceae as bulbous plants with umbellate inflorescences, the latter characteristic being the defining feature: "an umbellate inflorescence subtended by an involucre of one or more spathaceous bracts".
His work on this has been upheld by subsequent research and his definition remains valid today. Using this criterion, he removed a number of taxa (
Agavaceae,
Hypoxidaceae,
Alstroemeriaceae) and transferred the
Agapantheae,
Allieae, and
Gilliesieae from Liliaceae to Amaryllidaceae. Other writers proposed reuniting Amaryllidaceae with Liliaceae.
Thorne (1976) and
Cronquist (1988) both included Amaryllidaceae within a broad concept of Liliaceae (although Thorne later separated them again, but keep Alliaceae as a third family). Thus 'Alliaceae' were variously included in either Liliaceae, Amaryllidaceae, or as a separate entity. This uncertainty of circumscription reflected a wider problem with the
petaloid monocots in general. Over the course of time, widely differing views as to the limits of the family have been expressed, so much of the literature dealing with this family requires careful inspection to determine which sense of the Amaryllidaceae the work treats.
Phylogenetic era The current
phylogenetic era of understanding the taxonomic relationships of Amaryllidaceae began with the work of
Fay and
Chase (1996) who used the
plastid gene rubisco rbcL to identify the close relationship between
Agapanthus,
Alliaceae, and Amaryllidaceae.
Agapanthus had variously been included in Alliaceae or was placed in a separate family, Agapanthaceae. They relocated
Agapanthus within Amaryllidaceae as they considered it a
sister group to that family. Nevertheless, the
Angiosperm Phylogeny Group (APG)
classification (1998) still considered these three separate families within Asparagales. The close relationship was confirmed in a more detailed study by
Meerow (1999) who confirmed the
monophyly of Amaryllidaceae, with Agapanthaceae as its sister family and Alliaceae in turn as sister to the Amaryllidaceae/Agapanthaceae
clade. In its
second iteration (2003), the APG proposed simplifying the higher (core) Asparagales by reducing them to two more broadly circumscribed families, and provisionally proposed the name Alliaceae
sensu lato (
s.l.) to include the three sister families (Agapanthaceae, Alliaceae
sensu stricto,
s.s., and Amaryllidaceae), since together they form a monophyletic group. In this respect, they were following Hutchinson's system (see above). Under this proposal, the three families became reduced to subfamilies (and by extension the subfamilies of Alliaceae
s.s. being reduced to tribes.) At the same time, they appreciated an argument existed for making Amaryllidaceae
s.l. the formal name of the new and larger family, a position subsequently strongly supported by Meerow and colleagues. The
2009 version of the APG formally adopted this broad view and the conserved name Amaryllidaceae. To distinguish this broader family from the older, narrower family, it has become customary to refer to Amaryllidaceae
sensu APG, or as used by APG, Amaryllidaceae
s.l.. as opposed to Amaryllidaceae
s.s.. This
phylogenetic tree (
cladogram) shows the placement of Amaryllidaceae
s.l. within the order Asparagales. }} }} }} }} }} }} }} }} }} }} }} }} }} }}
Subdivision As reconstituted by the APG, Amaryllidaceae
s.l. consists of three
subfamilies, Agapanthoideae, Allioideae, and Amaryllidoideae, corresponding to the three families that were subsumed into it: •
Agapanthoideae (Agapanthaceae) •
Allioideae (Alliaceae) •
Amaryllidoideae (Amaryllidaceae
s.s.) Of these, one (Agapanthoideae) is
monogeneric for
Agapanthus (see Cladogram I). }} }} Of the other two subfamilies, Allioideae was resolved into three subdivisions by the initial
phylogenetic studies of Fay and Chase (1996). Since they treated Allioideae as family Alliaceae, these were subfamilies Allioideae, Tulbaghioideae, and Gilliesioideae. When family Alliaceae was reduced to subfamily Allioideae, they were reduced to tribes, namely Allieae, Tulbaghieae and Gilliesieae (see Cladogram II). }} }} Complete resolution of infrafamilial (suprageneric) relationships within subfamily Amaryllidoideae (Amaryllidaceae
s.s.) has proven more difficult. Fay and Chase's study lacked sufficient resolution for further elucidation of this group. Historically a wide variety of infrafamilial classification systems have been proposed for the Amaryllidaceae. In the latter twentieth century there were at least six schemes, including
Hutchinson (1926),
Traub (1963), }} }} }} }} }} }} }} }} }} }} }} }} }} }} }}
Angiosperm Phylogeny Group Publication of the third version of the APG classification and acceptance of Amaryllidaceae
s.l. was accompanied by a listing of accepted subfamily and tribal names, since the change in
rank from family to subfamily necessitated a revision of other lower ranks, as follows: Family: Amaryllidaceae
J.St.-Hil., Expos. Fam. Nat. 1: 134. Feb–Apr 1805,
nom. cons. • Subfamily:
Agapanthoideae Endl., Gen. Pl.: 141. Dec 1836. (1 genus) • Subfamily:
Allioideae Herb., Amaryllidaceae: 48. late Apr 1837. • Tribe
Allieae Dumort., Fl. Belg.: 139. 1827. (1 genus) • Tribe
Gilliesieae Baker, J. Linn. Soc., Bot. 14: 509. 24 April 1875. (18 genera) • Tribe
Tulbaghieae Endl. ex
Meisn., Pl. Vasc. Gen.: Tab. Diagn. 397, 399, Comm. 302. 17–20 Dec 1842. (2 genera) • Subfamily:
Amaryllidoideae Burnett, Outl. Bot.: 446. Feb 1835 (15 tribes) • Tribe
Amaryllideae Dumort., Anal. Fam. Pl.: 58. 1829. • Tribe
Calostemmateae D.Müll.-Doblies & U.Müll.Doblies, Feddes Repert. 107 (Short commun.): 7 December 1996. • Tribe
Cyrtantheae Traub, Herbertia 5: 111. Nov 1938. • Tribe
Eucharideae Hutch., Fam.Fl.Pl.2:130.20 Jul 1934. • Tribe
Eustephieae Hutch., Fam.Fl.Pl.2:130.20 Jul 1934. • Tribe
Galantheae Parl., Fl. Ital. 3: 75. 1858. • Tribe
Gethyllideae Dumort., Anal. Fam. Pl.: 58. 1829. • Tribe
Haemantheae Hutch., Fam. Fl. Pl. 2: 130. 20 July 1934. • Tribe
Hippeastreae Herb. ex
Sweet, Brit. Fl. Gard., ser. 2, 1: ad t. 14. 1 September 1829. • Tribe
Hymenocallideae Small, Man. S.E. Fl.: 315. 30 November 1933. • Tribe
Lycorideae Traub ex D.Müll.-Doblies & U.Müll.Doblies, Feddes Repert. 107 (Short commun.): 6. Dec. 1996. • Tribe
Narcisseae Lam. & DC., Syn. Pl. Fl. Gall.: 165. 30 June 1806. • Tribe
Pancratieae Dumort., Anal. Fam. Pl.: 58. 1829. • Tribe
Stenomesseae Traub, Pl. Life 19: 60. Jan 1963 This circumscription differs from the phylogenetic descriptions of Meerow and colleagues in several respects. Griffineae is recognised as a distinct tribe within the Hippeastroid clade, and Stenomesseae is recognised as
polyphyletic with two distinct types based on leaf shape (
lorate-leafed and
petiolate-leafed). The lorate-leafed species of the type genus of Stenomesseae,
Stemomesson, were transferred to a new tribe, Clinantheae as sister to Hymenocallideae in the Andean clade. The remnants of
Stemomesson then formed a distinct clade with
Eucharis (Eucharidae) and Eucharidae renamed as Stenomesseae (see
Cladogram III). • Tribe
Griffineae Ravenna • Tribe
Clinantheae Meerow '' holotype fossil
Genera Plants of the World Online accepts 71 genera. and the 2018 description of
Ypresian age
bulbils as
Paleoallium were the first Amaryllidaceae . •
Acis •
Agapanthus •
Allium •
Amaryllis •
Ammocharis •
Apodolirion •
Atacamallium •
Boophone •
Brunsvigia •
Calostemma •
Cearanthes •
Chlidanthus •
Clinanthus •
Clivia •
Crinum •
Crossyne •
Cryptostephanus •
Cyrtanthus •
Eucrosia •
Eustephia •
Galanthus •
Gethyllis •
Gilliesia •
Griffinia •
Haemanthus •
Hannonia •
Hessea •
Hieronymiella •
Hippeastrum •
Hymenocallis •
Ipheion •
Ismene •
Lapiedra •
Latace •
Leptochiton •
Leucocoryne •
Leucojum •
Lycoris •
Mathieua •
Miersia •
× Myobranthus •
Namaquanula •
Narcissus •
Nerine •
Nothoscordum •
Pamianthe •
Pancratium •
Paposoa •
Paramongaia •
Phaedranassa •
Phycella •
Plagiolirion •
Proiphys •
Pyrolirion •
Rauhia •
Rhodolirium •
Scadoxus •
Schickendantziella •
Shoubiaonia •
Sprekelia •
Stenomesson •
Sternbergia •
Strumaria •
Traubia •
Trichlora •
Tristagma •
Tulbaghia •
Ungernia •
Urceolina •
Vagaria •
Worsleya •
Zephyranthes == Distribution ==