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spurge family

Habit Herbs, annual or perennial [rarely shrubs or small trees], with taproot or tuberous rootstock. Herbs, subshrubs, shrubs, trees, or vines [lianas], annual, biennial, or perennial, deciduous or evergreen, monoecious or dioecious; latex present or absent.
Stems

erect or ascending, branched, terete, glabrous or hairy.

Leaves

opposite or alternate;

stipules usually present, occasionally absent, at base of petiole;

petiole present, glabrous or hairy;

blade monomorphic (occasionally polymorphic in E. cyathophora and E. heterophylla), base symmetric, margins entire or toothed, flat to revolute, surfaces glabrous or variously hairy;

venation pinnate, midvein often prominent.

alternate, opposite, whorled, or fascicled on short shoots, simple (3-foliolate in Tragia laciniata) [palmately compound];

stipules present or absent;

petiole present or absent;

blade sometimes palmately lobed, margins entire, subentire, repand, crenate, serrate, or dentate;

venation pinnate, palmate, or palmate at base and pinnate distally.

Inflorescences

unisexual or bisexual, axillary, terminal, or leaf-opposed [cauliflorous], racemes, panicles, spikes, thyrses, cymes, fascicles, or pseudanthia, or flowers solitary.

Involucre

± actinomorphic, not spurred;

glands 1–3 (sometimes 4–5 in E. eriantha, E. exstipulata, and E. radians), sessile or stipitate, shallowly cupped to deeply concave;

appendages absent or petaloid (E. bifurcata, E. eriantha, and E. exstipulata).

Flowers

unisexual;

perianth hypogynous;

hypanthium absent;

sepals 0 or 2–12, distinct or connate basally to most of length;

petals 0 or (3–)5(–6), distinct or connate;

nectary present or absent;

stamens 1–35(–1000), distinct or connate, free;

anthers dehiscing by longitudinal slits;

pistil 1, (1–)3–5(–20)-carpellate, ovary superior, (1–)3–5(–20)-locular, placentation axile;

ovules 1 per locule, anatropous;

styles 1–5(–9), distinct or connate, unbranched, 2-fid, or multifid;

stigmas 1–32+.

Staminate flowers

3–25.

Pistillate flowers

ovary glabrous or hairy;

styles distinct, occasionally appearing connate at base, unbranched or 2-fid.

Fruits

usually capsules, dehiscence septicidal, (usually schizocarpic with cocci separating from persistent columnella, coccus usually dehiscent loculicidally), sometimes schizocarps, drupes, or achenes [berries].

Seeds

caruncle present or absent.

1 per locule.

Cyathial

arrangement: terminal monochasia, dichasia, or condensed pleiochasia with 1–3 primary branches;

individual pleiochasial branches unbranched or few-branched at 1 or more successive nodes;

bracts subtending pleiochasia (pleiochasial bracts) opposite or whorled, usually wholly green or with paler green, white, pink, or red at base, sometimes wholly white, pink, or red, similar in shape and size to distal leaves or distinctly different, those on branches and subtending cyathia (dichasial and subcyathial bracts) opposite, distinct;

additional cymose branches occasionally present in axils of distal leaves, but alternately arranged and without whorled bracts.

x

= 7.

Euphorbia sect. Poinsettia

Euphorbiaceae

Distribution
North America; Mexico; Central America; South America; West Indies; Eurasia; Africa; Indian Ocean Islands; Pacific Islands; Australia
North America; Mexico; Central America; South America; West Indies; Bermuda; Eurasia; Africa; Atlantic Islands; Indian Ocean Islands; Pacific Islands; Australia; mostly tropical to warm temperate regions
[BONAP county map]
Discussion

Species ca. 30 (10 in the flora).

Section Poinsettia belongs to Euphorbia subg. Chamaesyce (Gray) Reichenbach. An expanded sect. Poinsettia is recognized here to include three species that have previously often been included in sect. Alectoroctonum (Schlechtendal) Baillon (E. bifurcata, E. eriantha, and E. exstipulata). These three species differ from the so-called core Poinsettia by the presence of involucral gland appendages, but they possess the shallowly to deeply concave involucral glands and toothed leaves that are generally diagnostic for the broader section. Molecular phylogenetic analyses clearly unite these three species with the other members of sect. Poinsettia and not with sect. Alectoroctonum (Y. Yang et al. 2012).

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Genera ca. 220, species ca. 6500 (24 genera, 259 species in the flora).

Molecular phylogenetic studies have shown Euphorbiaceae, as traditionally treated (A. Radcliffe-Smith 2001; G. L. Webster 1994b, 2014), to be polyphyletic, forming several groups in Malpighiales (C. C. Davis et al. 2005; T. Tokuoka and H. Tobe 2006; K. Wurdack and Davis 2009; Z. Xi et al. 2012). The treatment here reflects those findings. Genera formerly placed in subfamilies Oldfieldioideae Eg. Köhler & G. L. Webster and Phyllanthoideae Beilschmied, characterized by two ovules per locule, are treated as Picrodendraceae and Phyllanthaceae respectively, with two genera segregated from the latter as Putranjivaceae; the first two families appear to be sister taxa, possibly near much of the remaining traditional Euphorbiaceae, whereas the third is placed elsewhere in Malpighiales (Xi et al. 2012). The remaining genera, characterized by one ovule per locule, are treated as Euphorbiaceae in the strict sense and Peraceae Klotzsch (not represented in the flora area).

Four subfamilies currently are recognized in the narrowly defined Euphorbiaceae (K. Wurdack et al. 2005; G. L. Webster 2014). Traditionally, three subfamilies, Acalyphoideae Beilschmied, Crotonoideae Beilschmied, and Euphorbioideae Beilschmied, were recognized based on laticifer presence or absence and pollen morphology (A. Radcliffe-Smith 2001; Webster 1994b). Phylogenetic analyses of molecular data (Wurdack et al.; T. Tokuoka 2007) support the monophyly of Euphorbioideae, represented in the flora area by Ditrysinia, Euphorbia, Gymnanthes, Hippomane, Hura, Microstachys, Pleradenophora, Stillingia, and Triadica. Most of the traditional Crotonoideae is moderately supported as monophyletic, including Astraea, Cnidoscolus, Croton, Jatropha, Manihot, and Vernicia in the flora area. These studies also strongly support the monophyly of most of Acalyphoideae (including Acalypha, Adelia, Argythamnia, Bernardia, Caperonia, Dalechampia, Mercurialis, Ricinus, and Tragia in the flora area), and segregation of a fourth, small subfamily, Cheilosoideae K. Wurdack & Petra Hoffmann (not represented in the flora area). The remaining genera of Acalyphoideae and Crotonoideae, none of which are in the flora area, were placed in several small clades whose relationships to each other and to the four subfamilies were not well supported.

Euphorbiaceae in the strict sense are diverse morphologically, but most are characterized by schizocarpic capsules in which the cocci separate from the persistent columella, often explosively; the seeds are dispersed when the cocci split septicidally and usually also loculicidally. Similar capsules also are found in many Phyllanthaceae and Picrodendraceae but, as noted above, they have two ovules per locule, versus one in Euphorbiaceae. White or whitish latex is found in Euphorbioideae and colored latex in many Crotonoideae, whereas Acalyphoideae lack latex. Pseudanthia evolved independently and are structurally different in Dalechampia and Euphorbia.

Euphorbiaceae are most species-rich and ecologically important in tropical and subtropical regions. The same is true of genera found in the flora area, many of which are represented there only by a small proportion of their global diversity.

Notable economically important Euphorbiaceae are Hevea Aublet, a major source of rubber; Manihot, cassava or manioc, the starchy tubers of which are a major food source in much of the tropics; Ricinus, the source of castor oil; and Vernicia (and its close relative Aleurites J. R. Forster & G. Forster), sources of tung and other finishing oils. Some species of Euphorbiaceae are used horticulturally, especially members of Euphorbia; probably the best known of these is the poinsettia, E. pulcherrima Willdenow ex Klotzsch. Also well-known is Codiaeum variegatum (Linnaeus) A. Jussieu, the horticultural croton. Some introduced Euphorbiaceae have become problematic invasives in the flora area, particularly in areas with mild climates. Most notable among these invasive species are leafy spurge (Euphorbia virgata, commonly incorrectly called E. esula), Chinese tallowtree (Triadica sebifera), and tung-oil tree (Vernicia fordii).

Mallotus japonicus (Linnaeus f.) Müller Arg., food wrapper plant, has escaped locally in Durham and Orange counties, North Carolina. The Orange County population may have been eradicated and the status of the Durham County population is not known. This dioecious shrub or small tree, native to eastern Asia, has stellate hairs and in the key below would come under the first lead of couplet 5 with Astraea, Bernardia, and Croton. It can be distinguished from those three genera by its pale yellow to white glandular scales on the leaves and stems, staminate flowers with 70–100 stamens, unbranched styles, and ovaries and capsules covered with soft spines and reddish orange glandular scales.

Sapium haematospermum Müller Arg. from South America was collected on ballast in Pensacola, Florida, in 1901; this collection generally has been incorrectly reported as S. glandulosum (Linnaeus) Morong. Although the species does not appear to have become naturalized in the flora area, it could become adventive in subtropical areas. In the key below, S. haematospermum would come under the second lead of couplet 12 and can be distinguished from the five genera there by its combination of petioles with apical glands, inflorescences with two glands subtending each bract, staminate flowers with two to three sepals that are connate basally, pistillate flowers with three-carpellate pistils bearing three styles, and seeds covered in a red aril.

In the key and descriptions below, laminar glands are those borne on the surface of the leaf blade, not those extending from the margins or teeth or borne at the leaf base at the junction with the petiole.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Leaf blades linear to linear-elliptic, margins entire or with 2–4 inconspicuous teeth near apex; involucral glands densely canescent, appendages divided into subulate segments, incurved and covering glands, densely canescent; styles unbranched.
E. eriantha
1. Leaf blades linear, lanceolate, ovate, oblong, elliptic, or pandurate, margins conspicuously toothed (sometimes subentire in E. cyathophora, entire or few toothed in E. pinetorum); involucral glands glabrous, appendages absent or entire, undulate, slightly lobed, or divided into triangular segments, not incurved and covering glands, glabrous; styles 2-fid.
→ 2
2. Branches often arcuate; involucral gland appendages usually present, rarely absent.
→ 3
3. Leaf blades usually ovate, rarely oblong or elliptic, margins finely serrulate; petioles 15–49 mm; involucral glands 1(–3); ovaries glabrous; caruncles absent or rudimentary.
E. bifurcata
3. Leaf blades linear to narrowly elliptic or ovate, margins coarsely serrate; petioles 1–3 mm; involucral glands 4 (–5); ovaries puberulent on keels; caruncles 0.1 × 0.2 mm.
E. exstipulata
2. Branches ± straight (except occasionally proximal branches arcuate in E. davidii and E. dentata); involucral gland appendages absent.
→ 4
4. Leaves usually opposite, occasionally alternate distally, blade margins coarsely crenate-dentate or doubly crenate; seeds with caruncles; pleiochasial bracts wholly green or with paler green, white, or mauve near base; annual herbs.
→ 5
5. Ovaries densely pilose; capsules pilose (often sparsely); involucral gland taller than wide, stipitate.
E. cuphosperma
5. Ovaries and capsules glabrous or sparsely strigose; involucral glands shorter than wide, sessile.
→ 6
6. Hairs of abaxial leaf blade surface stiff, strongly tapered; capsules 4–4.8 mm wide; seeds angular in cross section, unevenly tuberculate.
E. davidii
6. Hairs of abaxial leaf blade surface weak, filiform; capsules 3.5–4 mm wide; seeds rounded in cross section, evenly tuberculate.
E. dentata
4. Leaves usually alternate, occasionally opposite proximally, blade margins entire, subentire, or glandular-serrulate; seeds usually without caruncles, occasionally caruncles rudimentary; pleiochasial bracts green (purpurescent in E. pinetorum), often paler green, white, pink, or red at base, occasionally wholly white, pink, or red; annual or perennial herbs.
→ 7
7. Stems 5–20(–30) cm, from moniliform tuberous rootstocks; seeds 4–4.6 mm; perennial herbs.
E. radians
7. Stems 20–100 cm, with taproots or woody rootstocks; seeds 2.1–3.1 mm; annual or perennial herbs.
→ 8
8. Pleiochasial bracts wholly green or paler green at base; involucral glands stipitate, opening round (occasionally flattened from pressing), with annular rim.
E. heterophylla
8. Pleiochasial bracts green or purpurescent, often white, pink, or red at base, occasionally wholly white, pink, or red; involucral glands sessile or substipitate, opening oblong (flattened without pressing), without annular rim.
→ 9
9. Annual herbs with spreading taproots; leaf blades 4–40 mm wide, linear, lanceolate, elliptic, or broadly pandurate; bracts usually green with white, pink, or red at base, occasionally distal bracts wholly white, pink, or red, rarely all bracts wholly green; capsules green; involucral gland 1; widespread, including s Florida.
E. cyathophora
9. Perennial herbs with thickened, woody taproots; leaf blades 2.5–5 mm wide, lanceolate to linear; bracts wholly purpurescent green or pink at base; capsules purpurescent; involucral glands 3(–5); Miami-Dade and Monroe counties, s Florida.
E. pinetorum
1. Inflorescences pseudanthia, each consisting of an involucre enclosing 1 or 3 pistillate flowers and (0–)1–80 staminate flowers.
→ 2
2. Vines; pseudanthia with involucre of 2 showy bracts and 3 pistillate flowers; latex absent.
Dalechampia
2. Herbs, subshrubs, or shrubs; pseudanthia with cuplike involucre and 1 pistillate flower; latex white.
Euphorbia
1. Inflorescences thyrses, cymes, racemes, panicles, spikes, or fascicles, or flowers solitary.
→ 3
3. Stinging hairs present (sometimes inconspicuous in Tragia except on ovaries and capsules).
→ 4
4. Sepals usually green, sometimes reddish green, not petaloid; inflorescences racemes; petioles without glands at apices; latex absent.
Tragia
4. Sepals white, petaloid; inflorescences dichasial cymes; petioles with glands at apices; latex white.
Cnidoscolus
3. Stinging hairs absent.
→ 5
5. Hairs stellate or scalelike, sometimes also unbranched.
→ 6
6. Stamens ± straight in bud; laminar glands abaxial, crateriform; staminate petals 0, nectaries intrastaminal; latex absent; caruncle absent.
Bernardia
6. Stamens inflexed in bud; laminar glands absent; staminate petals 0 or (3–)5(–6), nectaries extrastaminal; latex usually present, colorless to reddish; caruncle present.
→ 7
7. Leaf blades usually palmately lobed, sometimes unlobed; hairs unbranched and stellate; pistillate sepals usually not touching in bud; seeds rectangular-oblong.
Astraea
7. Leaf blades unlobed; hairs stellate or scalelike; pistillate sepals imbricate or valvate; seeds ellipsoid, oblong, ovoid, globose, or lenticular.
Croton
5. Hairs unbranched, malpighiaceous, 2-fid, or absent.
→ 8
8. Leaves opposite or subopposite.
→ 9
9. Latex absent; plants dioecious; inflorescences axillary; capsules hispid.
Mercurialis
9. Latex white; plants monoecious; inflorescences terminal; capsules glabrous.
Stillingia
8. Leaves alternate or fascicled.
→ 10
10. Glands subtending each inflorescence bract 2 or 10–14.
→ 11
11. Leaf blades palmately lobed; stamens to 1000; pistillate sepals 5; styles 2-fid.
Ricinus
11. Leaf blades unlobed; stamens 2–3; pistillate sepals 0 or 2–3; styles unbranched.
→ 12
12. Pistils 6–9-carpellate; fruits drupes.
Hippomane
12. Pistils 2–3-carpellate; fruits capsules.
→ 13
13. Glands subtending inflorescence bracts 10–14; pistillate sepals 2; pistils 2-carpellate; styles 2.
Pleradenophora
13. Glands subtending inflorescence bracts 2; pistillate sepals 0 or 3; pistils 3-carpellate; styles 3.
→ 14
14. Petioles with glands at apices; staminate sepals connate most of length; outer seed coat fleshy.
Triadica
14. Petioles without glands at apices; staminate sepals distinct or connate basally; outer seed coat dry.
→ 15
15. Plants without hairs; staminate sepals 2; stamens 2; capsule base persisting as 3-lobed gynobase.
Stillingia
15. Plants with hairs; staminate sepals 3; stamens 3; capsule base not persisting.
→ 16
16. Herbs, annual; latex white; leaf blade margins serrulate.
Microstachys
16. Shrubs; latex absent; leaf blade margins entire.
Ditrysinia
10. Glands subtending each inflorescence bract 0.
→ 17
17. Petals 5(–6) (pistillate sometimes rudimentary or 0 in Argythamnia).
→ 18
18. Sepals 2(–3); petioles with glands at apices; petals longer than 24 mm; inflorescences paniclelike thyrses.
Vernicia
18. Sepals 5–8(–10); petioles without glands at apices (sometimes stipitate-glandular or with tack-shaped glands along length); petals less than 18 mm or absent; inflorescences cymes, fascicles, racemes, or spikes, or flowers solitary.
→ 19
19. Latex colorless, cloudy-whitish, yellow, or red; inflorescences cymes or fascicles, or flowers solitary; staminate sepals imbricate; leaf blades palmately lobed or unlobed.
Jatropha
19. Latex absent; inflorescences spikes or racemes; staminate sepals valvate; leaf blades unlobed.
→ 20
20. Leaf blade secondary veins arcuate, not closely spaced; styles 2-fid, branches 6 per flower; capsules not muricate; flower nectaries 5 glands; hairs usually malpighiaceous, sometimes unbranched, rarely absent.
Argythamnia
20. Leaf blade secondary veins straight, closely spaced; styles deeply multifid, branches 12–21 per flower; capsules muricate; flower nectaries absent; hairs unbranched.
Caperonia
17. Petals 0 (sepals petaloid in Manihot).
→ 21
21. Petioles with conspicuous lateral glands at apex; pistils 5–20-carpellate; style 1; stamens 10–80, connate entire length forming thick column; trees, trunks with broad-based conic thorns.
Hura
21. Petioles with inconspicuous adaxial glands at apex or glands absent; pistils (1–)3(–4)-carpellate; styles (1–)3(–4), equal to carpel number; stamens (2–)4–17, distinct or connate basally; herbs, subshrubs, shrubs, or trees, unarmed (branchlets sometimes stiff and thorn-tipped in Adelia).
→ 22
22. Inflorescences racemes or panicles; staminate sepals 5, petaloid, 7–20 mm, connate 1/2 length; latex white; leaf blades usually deeply palmately lobed, rarely unlobed.
Manihot
22. Inflorescences fascicles or racemelike or spikelike thyrses, or flowers solitary; staminate sepals 0 or 4–5, not petaloid, 1–2 mm, distinct; latex colorless or absent; leaf blades unlobed.
→ 23
23. Sepals 0; latex colorless; styles unbranched; stamens (2–)4(–5).
Gymnanthes
23. Staminate sepals 4–5, pistillate sepals 3 or 5(–6); latex absent; styles usually multifid or laciniate, rarely 2-fid or unbranched; stamens 4–8 or 14–17.
→ 24
24. Leaves alternate, blade margins serrate or crenate to subentire; inflorescences spikelike thyrses; bracts subtending pistillate flowers enlarging in fruit; stamens 4–8; pistillate sepals 3.
Acalypha
24. Leaves fascicled on short shoots, blade margins entire; inflorescences fascicles or flowers solitary; bracts subtending pistillate flowers minute, not enlarging in fruit; stamens 14–17; pistillate sepals 5(–6).
Adelia
Source FNA vol. 12, p. 317. Authors: Jess A. Peirson, Paul E. Berry, Victor W. Steinmann. FNA vol. 12, p. 156. Authors: Geoffrey A. Levin, Lynn J. Gillespie.
Parent taxa Euphorbiaceae > Euphorbia
Subordinate taxa
E. bifurcata, E. cuphosperma, E. cyathophora, E. davidii, E. dentata, E. eriantha, E. exstipulata, E. heterophylla, E. pinetorum, E. radians
Acalypha, Adelia, Argythamnia, Astraea, Bernardia, Caperonia, Cnidoscolus, Croton, Dalechampia, Ditrysinia, Euphorbia, Gymnanthes, Hippomane, Hura, Jatropha, Manihot, Mercurialis, Microstachys, Pleradenophora, Ricinus, Stillingia, Tragia, Triadica, Vernicia
Synonyms Poinsettia
Name authority (Graham) Baillon: Étude Euphorb., 284. (1858) Jussieu
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